The automation and standardization of hyperspectral imaging, particularly at high spatial resolution, are essential for advancing plant phenomics and supporting diverse plant science research. We developed HyperBird, a hyperspectral microscopic imaging robot, to automate the acquisition of up to 351 leaf-disc samples in a single tray within approximately 2.4 h and thereby support scalable plant experiments. System calibration established a spatial resolution of 24.3 μ m (full width at half maximum; FWHM), a spectral resolution of 1.78 nm (FWHM), and a depth of field of 4.53 mm, producing hyperspectral data cubes of 2195 × 2000 × 950 pixels across the 400–1000 nm spectral range. System-level and biological-sample consistency assessments confirmed stable spectral measurements during extended scanning sessions and across independently prepared trays. Thermal evaluation confirmed that the 150 W illumination design introduced minimal sample heating during scanning. HyperBird was first evaluated using grape downy and powdery mildews, where no consistent measurable effect of repeated imaging on pathosystem development was detected under the tested experimental conditions. Subsequently, HyperBird was used to characterize spatiotemporal spectral progression in grapevine leaves inoculated with Plasmopara viticola . An automated regional spectral tracing pipeline was developed to isolate spectra from retrospectively traced regions and compare them with whole-leaf averaged spectra across 0–9 days post-inoculation (DPI). Categorical mixed-effects modeling showed that these spatially resolved regional spectra exhibited significant disease-associated spectral change by 5 DPI, with a sharp transition at 6 DPI, whereas whole-leaf spectra showed delayed and weaker disease-aligned changes beginning at 7 DPI. These results demonstrate that HyperBird enables high-throughput, spatially resolved hyperspectral imaging for quantifying localized plant disease progression and provides a scalable platform for studying spectral biology across plant phenotyping applications.
Why it matches plant phenotyping methodsHyperBirdの高スループット・ハイパースペクトル画像取得ロボットを開発し、校正、再現性、加熱影響、病害進展の定量性能を検証しており、植物フェノタイピング手法が中心である。
abstractWe developed HyperBird, a hyperspectral microscopic imaging robot, to automate the acquisition of up to 351 leaf-disc samples in a single tray within approximately 2.4 h and thereby support scalable plant experiments.
Reproduction assets foundThe paper's Data Availability statement points to a public GitHub repository containing the authors' code and processed data supporting the phenotyping analyses; raw hyperspectral image data are request-only.Code · publicData Availability
857
The code and processed data supporting the findings of this study are available in the GitHub
858
repository at https://github.com/jy773Cornell/HyperBird-Robot. Raw hyperspectral image
859
data are available from the corresponding author upon reasonable request due to file size and storage
860
constraints.
861
Supplementary Materials
862
Supplementary materials accompany this article as a separate document (supplementary.pdf).
863
Supplementary Figure S1. Representative GSAM-based segOpen asset ↗HyperBird-Robotpdf-raw-page:39 lines:1-75Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
Surface phenotyping underpins plant science, preclinical animal research and entomology, yet across all three the measurement is almost always a photograph, which records a projection and not the surface itself. Here we present the Gentschinator3000 , an open structured-light platform that brings high-end metric surface measurement within reach of laboratories with no optics expertise, combining documented open hardware, open reconstruction software and analysis workflows for under 4000 Euro in components. It resolves a planar reference to 45 µm local flatness, registers full rotations to a loop closure of 156 µm, and performs stably across acquisition ranges that we define. Applying one workflow to a leaf before and after desiccation, to murine anatomy and to a spread lepidopteran, we find that projection underestimates surface area by 11 to 41 %. That error grows with the condition under study, with the evaluation scale and with the direction of view, so it can confound phenotype comparisons dramatically. In murine limbs a 15-degree change of viewing direction shifts a projected inter-segment angle by up to 23.2 degrees, while the three-dimensional angle does not move. Projection geometry can therefore contribute as much to a measured phenotype as the biology it is meant to quantify.
Why it matches plant phenotyping methods植物表面の三次元形状を測定するオープンな構造化光プラットフォームと再構成・解析ワークフローを開発し、葉で投影バイアスを評価しており、表現型取得手法が中心である。
abstractHere we present the Gentschinator3000 , an open structured-light platform that brings high-end metric surface measurement within reach of laboratories with no optics expertise, combining documented open hardware, open reconstruction software and analysis workflows for under 4000 Euro in components.
Reproduction assets foundThe paper explicitly deposits three public Zenodo records: reconstructed 3D surfaces of all specimens (including the leaf and hop cone phenotyping measurements), the authors' analysis notebooks with derived and per-panel source data, and the reconstruction software with build documentation and working examples. All areDataset · publicData availability
1149
The reconstructed surfaces supporting this study are available at Zenodo under
1150
https://doi.org/10.5281/zenodo.22167250.54
1151
Source data for all graph panels are provided with this paper; for panels showing
1152
rendered surfaces, the underlying reconstructions are in the same record.
1153
1154
Code availability
1155
The analysis notebooks, environment specifications, derived data and per-panel
1156
source data are available at Zenodo under
1Open asset ↗Zenodo · 10.5281/zenodo.22167250pdf-raw-page:35 lines:1-52Code · public1151
Source data for all graph panels are provided with this paper; for panels showing
1152
rendered surfaces, the underlying reconstructions are in the same record.
1153
1154
Code availability
1155
The analysis notebooks, environment specifications, derived data and per-panel
1156
source data are available at Zenodo under
1157
https://doi.org/10.5281/zenodo.22167598.55
1158
The reconstruction software, build documentation and minimal working examples
1159
are available at https://doi.org/10.5281/zenodo.22167471.56
1160
The software and analysis notebooks are released under the MIT licence and the
1161
hardware design files under CERN-OHL-P v2. The visible-light platform described
1162
hereOpen asset ↗Zenodo · 10.5281/zenodo.22167598pdf-raw-page:35 lines:1-52Code / dataset availability confirmedEurope PMC · Crossref · checked 14 Sept 2026
Abstract Deep convolutional networks now classify leaf images on curated benchmarks such as PlantVillage with accuracies close to the measurement ceiling of those datasets, which has shifted the open questions away from raw accuracy toward two under-reported issues: which components of a composite pipeline actually cause the result, and whether the components that matter on laboratory images are the same ones that matter on field photographs. We address both with a classification framework evaluated under a protocol that fixes every development decision before the independent test data are read. A Mask R-CNN stage localizes the dominant leaf, the accepted box is expanded by a validation-selected 5% margin and resized to a shared 224 by 224 input, and the same localized image is passed to ResNet50, InceptionV3, and MobileNetV2 together with an extractor that produces eighteen colour and shape descriptors. The forty-five class probabilities and eighteen descriptors form a sixty-three-dimensional input to a neural meta-classifier developed by three repetitions of stratified five-fold cross-validation. On a locked 3,101-image PlantVillage test partition of fifteen classes the framework reached 99.77% accuracy and 99.75% macro F1 with seven misclassifications, and a one-component-at-a-time ablation confirmed that every stage contributed. The same design was then trained and evaluated entirely within a separate thirteen-class PlantDoc field-image dataset, where it reached 90.03% accuracy and 89.40% macro F1. This is a within-PlantDoc experiment and not a controlled-to-field transfer test, so the figure measures how the pipeline behaves on field imagery rather than how a PlantVillage-trained model survives a domain shift. The central finding comes from running the identical ablation on both datasets: on clean images the ensemble breadth and descriptors provide the incremental gains, but under field conditions the ordering changes, and leaf localization and learned fusion become the decisive components. Removing localization cost 2.83 accuracy points and replacing the neural fusion with soft voting cost a further 2.08 points, the two largest effects on PlantDoc. The contribution is a controlled and transparent account of where each component of a localization-aware plant disease classifier earns its place, and of how that ordering shifts between laboratory and field acquisition.
Why it matches plant phenotyping methods葉画像から植物病害状態を推定する分類パイプラインの開発・アブレーション検証が中心であり、単なる病害実験や routine measurement ではない。
titleA Localization-Aware Heterogeneous CNN Ensemble with Neural Meta- Fusion for Plant Disease Classification, with a Component Analysis on Laboratory and Field Images
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Dataset · publicThe classification subset used here (20,638 images spanning fifteen pepper-bell, potato, and tomato classes) was obtained from PlantVillage, which is openly accessible at https://www.kaggle.com/datasets/emmarex/plantdisease.Open asset ↗Kaggle · emmarex/plantdiseaselines:314-336Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
Abstract Cross-sectional analysis is considered the reference method for measuring cotton fiber fineness and maturity; however, its widespread use has been limited by labor-intensive sample preparation and manual image analysis. The objective of this study was to develop and validate a reproducible deep-learning-based workflow for automated segmentation and quantitative analysis of cotton fiber cross-sections. A total of 249 composite light microscopy images of cotton fiber cross-sections were collected and manually annotated to generate training and validation datasets. A YOLO11m instance segmentation model was developed to identify cotton fiber and lumen regions and automatically extract quantitative traits, including fiber area, lumen area, fiber perimeter, and lumen perimeter. The workflow integrates automated image segmentation, post-processing, quantitative trait extraction, and data export to facilitate reproducible cotton fiber phenotyping. Model performance was evaluated using mean Average Precision (mAP), and workflow outputs were validated against Adobe Photoshop using descriptive comparisons of six cross-sectional traits. The model achieved Box mAP50 scores of 0.984 for cotton fiber regions and 0.789 for lumen regions, demonstrating high segmentation accuracy. The automated workflow substantially reduced manual analysis time while producing measurements with central tendencies comparable to those obtained using Adobe Photoshop. To facilitate reproducibility and adoption, the workflow, trained model weights, and supporting documentation are publicly available through GitHub and a Hugging Face web application. The workflow substantially increases analytical throughput while providing a reproducible and publicly accessible method for automated cotton fiber cross-sectional phenotyping, facilitating quantitative analysis for cotton genetics and breeding research.
Why it matches plant phenotyping methods綿繊維横断面の画像分割、形質抽出、検証を目的とした再現可能な深層学習ワークフローの開発であり、植物フェノタイピング手法が研究の中心である。
abstractThe objective of this study was to develop and validate a reproducible deep-learning-based workflow for automated segmentation and quantitative analysis of cotton fiber cross-sections.
Reproduction assets foundThe paper's cotton fiber cross-section phenotyping workflow (YOLO11m segmentation pipeline, trained model weights, example images/outputs) is explicitly stated as publicly available via a GitHub repository and a Hugging Face web application, with URLs matching the allowed list.Code · publicThe complete source code, training scripts, dataset configuration, example input images, example outputs,
and supporting documentation are publicly available through the GitHub repository:
https://github.com/RifeLab/cotton-lumen-microOpen asset ↗RifeLab/cotton-lumen-micropdf-page:11 lines:1-47Code · publicThe cotton fiber image analysis workflow is publicly available through a web-based application hosted on
Hugging Face at: https://huggingface.co/spaces/chaneylc/cotton_fiber_microscopy_measureOpen asset ↗pdf-page:11 lines:1-47Code / dataset availability confirmedCrossref · Europe PMC · checked 5 Sept 2026
Identifying plant health conditions is an emerging precision-agriculture and food-security challenge, intensified by deploying deep-learning models on memory- and power-constrained edge devices. We present a TinyMLOps pipeline spanning model design, optimization, quantization, and deployment across diverse edge devices, evaluated under controlled laboratory conditions. Using a dataset derived from the PlantVillage benchmark, 39 fine-grained classes are aggregated into three superclasses: healthy leaf, unhealthy leaf, and no leaves. The resulting system therefore performs plant health-status classification and background filtering rather than diagnosing specific diseases. We train a MobileNet-based convolutional neural network jointly optimized for classification accuracy and computational efficiency, adopting state-of-the-art hyperparameter optimization (HPO) tools. Five models are selected, four from the Pareto Front and one as the biggest evaluated model during HPO, converted to LiteRT and ONNX, and evaluated at float32 and post-training int8 precision on a Raspberry Pi Zero 2 W and an STM32H743ZI microcontroller. At float32, LiteRT is 1.87–2.65× faster than ONNX Runtime on the Raspberry Pi across all five models. Relative to their float32 LiteRT counterparts, the int8 LiteRT models are 2.83–3.67× smaller on disk and 21.3–31.2% faster on the same board, at a cost in F1-score of between 0.0010 and 0.0068. On the microcontroller, only the two smallest models deploy at both precisions; for these, the fully quantized int8 variants are 4.3× faster and 3.85× smaller in MCU flash footprint than the float32 counterparts. The mid-range model fits the 2 MB flash and 1 MB RAM budget only when quantized, while the two largest models exceed it in every configuration tested.
Why it matches plant phenotyping methods葉画像から植物の健康状態を推定する分類手法と、エッジデバイス向けの最適化・量子化・展開パイプラインが研究の中心であり、植物状態の画像ベースフェノタイピングに該当する。
abstractWe present a TinyMLOps pipeline spanning model design, optimization, quantization, and deployment across diverse edge devices, evaluated under controlled laboratory conditions.
Reproduction assets foundThe paper's plant-phenotyping measurements are based on a derived PlantVillage dataset (39 classes aggregated into three superclasses) that the authors explicitly state is openly available in their own GitHub repository, also catalogued in the AgrifoodTEF Data Space. No author analysis code or trained model checkpointsDataset · publicThe data used in this study are derived from the openly available GitHub repository available at https://github.com/FBK-OpenIoT/PlantVillage-AugNoLeaves , accessed on 1 July 2026.Open asset ↗FBK-OpenIoT/PlantVillage-AugNoLeaveslines:1355-1403Dataset · publicPlantVillage-AugNoLeaves—AgrifoodTEF Data Space Catalogue. 2025. [(accessed on 1 July 2026)]. Available online: https://dataspace.agrifoodtef.eu/asset/did:op:3091fdcf83a05784416e585e4e45ea24afaf8c925a891921a3949acd98426f65Open asset ↗did:op:3091fdcf83a05784416e585e4e45ea24afaf8c925a891921a3949acd98426f65lines:1424-1474Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
Idesia polycarpa Maxim. is a premier woody oil species in Guizhou Province, China, whose fruit yield and oil quality largely depend on effective pollination and fertilization. However, limited research on pollen viability and germination has hindered industrial progress. To address this gap, a comprehensive evaluation framework for elite I. polycarpa germplasm was developed, integrating micromorphological analysis, optimized staining protocols, and in vitro germination assay. Scanning electron microscopy (SEM) revealed that I. polycarpa pollen, while genetically conserved at the genus level-characterized by prolate shapes, tricolporate apertures, and reticulate exine ornamentation-exhibits notable micromorphological variation among genotypes. Of the nine staining protocols tested (2,3,5-triphenyl tetrazolium chloride [TTC], carbol fuchsin, acetocarmine, methylene blue, Alexander, peroxidase, 2,5-diphenylmonotetrazolium bromide [MTT], I2-KI, and red ink), TTC and red ink were the most effective, offering clear chromatic distinction between viable and non-viable pollen. Through orthogonal experimental designs, genotype-specific optimal media for in vitro germination were identified: 0.40 g/L H3BO3, 0.01 g/L KNO3, 0.02 g/L Ca(NO3)2·4H2O, and 0.20 g/L KH2PO4 for STZ-6; and 0.20 g/L H3BO3, 0.02 g/L KNO3, 0.02 g/L Ca(NO3)2·4H2O, and 0.10 g/L KH2PO4 for STZ-9. Regression analysis confirmed a highly significant positive correlation (P < 0.01) between in vitro germination rates and the staining results from both TTC and red ink across various concentrations. Notably, 5% TTC and 30% red ink exhibited the highest coefficients of determination. A hierarchical evaluation strategy is thus proposed: the 5% TTC method is recommended for precise laboratory quantification due to its stability, while the 30% red ink method, due to its ease of use, is suited for rapid field-based screening. This study provides valuable insights into the morphological characteristics of I. polycarpa pollen and establishes a standardized evaluation framework, supporting germplasm innovation and optimizing pollination management.
Why it matches plant phenotyping methods花粉の生存性・発芽という植物の生殖形質を対象に、染色法とin vitro発芽法を最適化・検証し、標準化した評価フレームワークを開発しているため、方法論が中心である。
abstracta comprehensive evaluation framework for elite I. polycarpa germplasm was developed, integrating micromorphological analysis, optimized staining protocols, and in vitro germination assay.
Reproduction assets foundThe article's Data Availability statement points to a public Biostudies deposit containing the study's data (pollen morphology measurements, staining viability counts, and in vitro germination results). No author analysis code or trained models are mentioned.Dataset · publicData Availability: The data that support the findings of this study are openly available in Biostudies at https://doi.org/10.6019/S-BSST3125 .Open asset ↗Biostudies · S-BSST3125lines:176-186Code / dataset availability confirmedCrossref · Europe PMC · checked 5 Sept 2026
Introduction Timely and accurate detection of plant diseases is essential for ensuring global food security and supporting sustainable agriculture. Conventional diagnostic approaches, such as manual inspection and laboratory testing, are often time-consuming, labor-intensive, and impractical for large-scale or remote agricultural environments. Although deep learning models, particularly Convolutional Neural Networks (CNNs), have significantly improved automated plant disease classification, they often lack interpretability and struggle to generalize under diverse field conditions. Methods This study proposes AgriX-SENet, an explainable deep learning framework that integrates Squeeze-and-Excitation (SE) blocks with a DenseNet121 backbone to enhance disease classification performance. The SE blocks recalibrate channel-wise feature responses to emphasize disease-relevant information while suppressing background noise. To improve model transparency, Grad-CAM, SHAP, and LIME were incorporated to provide visual and feature-level explanations of the model’s predictions. The framework was trained and evaluated using the Plant Pathology 2020 dataset containing four classes: healthy, rust, scab, and multiple diseases. Results AgriX-SENet achieved a training accuracy of 97.47% and a validation accuracy of 95.07%, outperforming fourteen state-of-the-art deep learning models. The classification report demonstrated high precision and recall across most disease categories, although the scab class exhibited comparatively lower recall, indicating an opportunity for further improvement. The explainability analyses consistently showed that the model focused on pathologically relevant regions of leaf images, validating the reliability of its predictions. Discussion The proposed AgriX-SENet framework effectively combines high classification performance with model interpretability, addressing a key limitation of existing CNN-based plant disease detection systems. Its ability to provide accurate and explainable predictions makes it a promising solution for scalable agricultural diagnostics. Future work will focus on improving classification performance for challenging disease categories and optimizing the framework for deployment on mobile and edge computing devices to enable real-time field applications.
Why it matches plant phenotyping methods葉画像から植物病害状態を推定する説明可能な深層学習フレームワークを開発・評価しており、植物表現型取得・判定手法が中心である。
abstractThis study proposes AgriX-SENet, an explainable deep learning framework that integrates Squeeze-and-Excitation (SE) blocks with a DenseNet121 backbone to enhance disease classification performance.
Reproduction assets foundThe paper trains and evaluates AgriX-SENet on the public Plant Pathology 2020 (FGVC7) Kaggle image dataset, which is the paper-specific plant image input for its disease-classification measurements. No author analysis code, trained model checkpoints, or supplementary code/data deposit is mentioned; the data statement (Dataset · publicPlant Pathology 2020 - Fgvc7 . Available online at: https://www.kaggle.com/competitions/plant-pathology-2020-fgvc7/data .Open asset ↗Kaggle · plant-pathology-2020-fgvc7lines:895-974Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
Premise Accurate species identification is crucial for ecological restoration and can be especially challenging for understudied non-model species. Quercus garryana is the only native oak species in the Pacific Northwest and is an important component of the endangered oak savanna ecosystem. Quercus robur is an imported ornamental species from Europe and has been found to be mistakenly planted as Q. garryana in habitat restoration projects. Methods We measured leaf morphological traits sampled from herbarium collections in their native ranges using the digital morphometric tools MorphoLeaf and Tomato Analyzer. We then used Lasso logistic analysis to generate a predictive model and tested it on leaves from Portland, Oregon. To streamline this species detection process, we developed Garryanalyzer, an ImageJ plug-in that automatically measures leaf traits and outputs species predictions. Results Garryanalyzer demonstrated 95% accuracy in predicting the species identity of herbarium specimens of oaks. Garryanalyzer correctly identified all Q. robur individuals sampled in Portland but showed lower accuracy for Q. garryana . Discussion Many existing morphometric software are not open source, which makes them unable to be customized to specific study systems. Garryanalyzer is built upon the widely used open-source ImageJ platform. This study also demonstrates a viable workflow for developing similar tools for other ecologically important non-model plant species.
Why it matches plant phenotyping methods葉の形態形質を自動測定し、種予測まで行うImageJプラグインとワークフローの開発・評価が中心であり、植物フェノタイピング手法として適格です。
abstractTo streamline this species detection process, we developed Garryanalyzer, an ImageJ plug-in that automatically measures leaf traits and outputs species predictions.
Reproduction assets foundThe paper's authors publicly released the Garryanalyzer ImageJ plug-in source code on GitHub, all original and modified leaf images used in the morphometric analyses on Zenodo, and the full leaf morphometric measurement dataset plus R Lasso analysis code in a second Zenodo repository. All are paper-specific, public,可直接Code · publicThe source code and installation instructions for Garryanalyzer can be accessed on GitHub at https://github.com/zxie8561/Garryanalyzer.Open asset ↗https://github.com/zxie8561/Garryanalyzer · zxie8561/Garryanalyzerhtml-lines:210-274Dataset · publicAll images used in the morphometric analyses, both original and modified, are available on Zenodo (https://doi.org/10.5281/zenodo.17462266).Open asset ↗https://doi.org/10.5281/zenodo.17462266 · 10.5281/zenodo.17462266html-lines:210-274Dataset · publicThe full dataset of leaf morphometric measurements of both GBIF and Portland samples, R code for Lasso analysis, and other miscellaneous files are available on a separate Zenodo repository (https://doi.org/10.5281/zenodo.17546152).Open asset ↗https://doi.org/10.5281/zenodo.17546152 · 10.5281/zenodo.17546152html-lines:210-274Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Ustilago maydis is a biotrophic fungus that causes smut disease in maize, leading to tumor formation on aerial parts of the plant. While U. maydis has been a model for plant-fungal interaction studies, no tool has existed to automatically quantify infection symptoms under laboratory conditions for deep learning analysis. To address this, we developed a rotating camera system that captures videos of plants under customized lighting and shutter settings. These videos were used to train machine learning models to distinguish between healthy and infected plants. Two detection approaches have been presented. In the first approach, by employing a naive masking technique and combining classical machine learning classifiers utilizing handcrafted features, the model achieved a reasonable performance, with an Area Under the Curve (AUC) of maximum 0.90 on the Receiver Operating Characteristic in one of the classifiers, showing relatively high sensitivity and specificity. The second approach utilizes pre-trained YOLO11 model for object detection and further classification. The YOLO11-based approach outperforms traditional methods, achieving near-perfect validation accuracy (AUC: 0.99-1.00), demonstrating its superiority for real-time, scalable applications. Our toolset, featuring a cost-efficient and customizable scanning platform with open building-blocks design, provides a valuable resource as a proof-of-concept for unbiased disease symptom detection and scoring, with potential applications in other plant pathology studies. This point enables easy replication and adaptation by other research laboratories which makes the platform robust, scalable and practical beyond our specific application.
Why it matches plant phenotyping methodsトウモロコシの感染症状を画像から自動検出・スコア化する低コスト撮像プラットフォームと機械学習手法の開発が中心であり、植物病害表現型の取得・抽出方法に該当する。
abstractwe developed a rotating camera system that captures videos of plants under customized lighting and shutter settings.
Background Cell geometry plays a central role in determining division orientation and body axis formation during early embryogenesis in Arabidopsis thaliana . However, quantitative analysis of dynamic three-dimensional (3D) morphology remains challenging because live-imaging studies often rely on two-dimensional (2D) projections, while existing 3D reconstruction approaches, including mesh-based methods, often lose the original orientation information relative to the ovule and require labor-intensive mesh correction. In addition, embryo positional fluctuation caused by floating in liquid medium and continuous growth makes it difficult to analyze temporal morphological changes within a common coordinate system. Results We developed a robust framework for quantitative 3D and four-dimensional (4D; 3D + time) analysis of embryo initial cell (apical cell) morphology. The method first establishes a standardized 3D coordinate system by normalizing cell orientation based on the bottom plane and the optical axis of the observation. Cell morphology is then reconstructed through ellipse-based approximation of serial cross-sections extracted from stacked imaging data, enabling accurate geometric characterization without the need for complex surface mesh reconstruction. To evaluate shape anisotropy, we quantified the apical cell shape in 3D. The framework further supports the characterization of volumetric features of subsequent division, providing a basis for quantifying 3D embryogenesis. Conclusion Our framework provides a simple and noise-reduced approach for quantitative analysis of living cell morphology in 3D. We named the integrated method of combining coordinate normalization with elliptical cross-section-based reconstruction Apical3DTip. This method enables consistent comparison of cell shapes without extensive manual corrections. The method overcomes key limitations of 2D projection-based and mesh-dependent analyses and offers a practical platform for quantifying cell shape and daughter cell shapes in 3D. More broadly, it provides a quantitative foundation for exploring the relationship between cell geometry, morphodynamics, and developmental patterning in living plant embryos.
Why it matches plant phenotyping methods植物胚の細胞形態を3D・4D画像から定量化する再構成手法を開発しており、表現型取得・抽出法が研究の中心である。
abstractWe developed a robust framework for quantitative 3D and four-dimensional (4D; 3D + time) analysis of embryo initial cell (apical cell) morphology.
Reproduction assets foundThe paper's Methods availability statement explicitly deposits the Apical3DTip analysis code and associated datasets on two public GitHub repositories (main implementation and ImageJ plugin). These are paper-specific author assets for the 3D/4D apical cell reconstruction and phenotyping analysis. No separate phenotype/Code · publicctor of the fitted vertical plane:
R ! .
Because the fitted plane passes through the centroid s, the offset e was calculated as
N
MQ.
Then, the fitted plane was represented as
O G N O
MQ 0.
Availability of data and materials
The code for Apical3DTip, along with all associated datasets, is available on Github:
https://github.com/blues0910/Apical3DTip.
Apical3DTip is also available as an ImageJ plugin:
https://github.com/YusukeKimata-Moo/Apical3DTip.
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Funding
This work was supported by a Japan Society for the PromotOpen asset ↗https://github.com/blues0910/Apical3DTippdf-layout-page:12 lines:1-49Code · publictroid s, the offset e was calculated as
N
MQ.
Then, the fitted plane was represented as
O G N O
MQ 0.
Availability of data and materials
The code for Apical3DTip, along with all associated datasets, is available on Github:
https://github.com/blues0910/Apical3DTip.
Apical3DTip is also available as an ImageJ plugin:
https://github.com/YusukeKimata-Moo/Apical3DTip.
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Funding
This work was supported by a Japan Society for the Promotion of Science (JSPS) KAKENHI
Grant (No. JP22K15135 to H.M., JP25H01809 to Y.K., JP26K02023 tOpen asset ↗https://github.com/YusukeKimata-Moo/Apical3DTippdf-layout-page:12 lines:1-49Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
Objective This study presents an integrated, multi-scale approach for the non-destructive estimation of phenological stages and carotenoid content in carrots by combining spectral techniques, colorimetry, and artificial intelligence. Methods Six commercial varieties, including orange, yellow, white, and purple genotypes, were evaluated under field and laboratory conditions using multispectral drone imagery, high-resolution spectroradiometric signatures, red green blue (RGB) images, and CIELAB color measurements. A hierarchical modeling framework was developed across two phases: (i) spectral modeling using uncrewed aerial vehicle (UAV)-based multispectral indices, textural and geometric metrics, and laboratory-generated hyperspectral signatures; and (ii) a colorimetric index from RGB images. Results Using UAV-based multispectral field data, phenological prediction indices achieved high classification performance (F1-scores > 0.90) when modeled with a Random Forest classifier, supported by distinct spectral signatures associated with canopy development and senescence. In parallel, carotenoid content estimation using a Random Forest regression model demonstrated strong predictive accuracy ( R 2 = 0.897; RMSE = 0.584), with the Plant Senescence Reflectance Index (PSRI) and Carotenoid Reflectance Index (CRI) identified as the most influential predictors. A complementary laboratory-based Random Forest regression model using high-resolution spectral signatures achieved near-perfect predictive performance ( R 2 = 0.987). SHapley Additive exPlanations (SHAP) analysis identified physiologically relevant wavelengths in the green (540-550 nm) and red-edge (∼700 nm) regions as the primary drivers of carotenoid concentration. Likewise, a novel colorimetric index (ICarot), derived from CIELAB parameters, enabled accurate image-based carotenoid estimation ( R 2 = 0.85). Conclusion This study introduces an innovative multi-sensor framework for precision agriculture and automated postharvest quality control, enabling rapid, objective, and scalable phenotyping in carrot production systems. Through the integration of spectral, colorimetric, and AI-based approaches, the proposed methodology effectively captures both internal nutritional attributes and external quality traits within a unified, non-destructive assessment pipeline.
Why it matches plant phenotyping methods複数センサー画像・分光計測とAIを統合し、ニンジンの生育段階およびカロテノイド含量を非破壊推定する手法を開発・評価しており、表現型取得が研究の中心である。
abstractThis study presents an integrated, multi-scale approach for the non-destructive estimation of phenological stages and carotenoid content in carrots by combining spectral techniques, colorimetry, and artificial intelligence.
Reproduction assets foundThe paper's Data Availability section explicitly deposits the study's data (and project materials) on GitHub and Zenodo, both with authors' public URLs matching allowed_urls. These qualify as paper-specific public assets for the carrot phenotyping measurements and analysis.Dataset · publicThe data is available at GitHub and Zenodo:
- https://github.com/agrocompuepidemlab/Carrot-value-chain-proyect/tree/mainOpen asset ↗github.com/agrocompuepidemlab/Carrot-value-chain-proyectlines:184-307Code / dataset availability confirmedarXiv · OpenAlex · checked 11 Sept 2026
Tomographic microscopy enables three-dimensional internal imaging but often requires expensive optical or X-ray instrumentation. Here we present an ultra-low-cost continuous-wave diffusive tomography (CWDT) system for biological samples. The system uses a smartphone microscope, a white LED coupled into an optical fiber, 3D-printed micropositioners, and a physics-based forward model optimized with machine learning. We demonstrate full-color volumetric reconstructions from a tartrazine-cleared poplar section, a scattering phantom, fungal mycelium near an Arabidopsis root, and thick poplar branch imaging with an inserted side-emitting fiber. The current results are qualitative and exploratory, but they show that scanned fiber illumination and inexpensive hardware can produce useful three-dimensional reconstruction outputs for low-cost microscopy experiments.
Why it matches plant phenotyping methods低コスト三次元断層イメージング法そのものを開発し、ポプラ組織・枝やシロイヌナズナ根近傍を対象に植物の内部構造を可視化しているため、植物形態の取得法として中心的です。
abstractHere we present an ultra-low-cost continuous-wave diffusive tomography (CWDT) system for biological samples.
Reproduction assets foundThe paper's raw imaging inputs, configurations, and reconstruction outputs for Figures 2–5 are publicly deposited on Kaggle. The analysis code repository is only 'prepared for release' (no confirmed public deposit yet), so it is listed as request-only. Hardware CAD mirrors are public but are instrument designs, not theDataset · publicFigure-level raw inputs, model configurations, selected outputs, and manifests are available through the Kaggle dataset https://www.kaggle.com/datasets/alingold/continuous-wave-diffusive-tomography .Open asset ↗continuous-wave-diffusive-tomographylines:108-129Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
Manually counting sunflower seeds on capitula is labor-intensive, requiring approximately one person-hour per head, and can be inconsistent for densely packed heads. Existing phenotyping approaches often depend on laboratory-based equipment, limiting their accessibility. In this study, we developed a benchtop image-based pipeline for rapid, non-destructive estimation of developed and aborted seeds on intact dried sunflower heads. A dataset of 1093 sunflower capitula was imaged under fixed indoor lighting, and individual seeds were annotated as developed or aborted. A YOLOv8m one-stage object detector was trained and evaluated using a counting-focused protocol, in which a single confidence threshold was selected on the validation set and then applied unchanged to an independent test set of 109 images. The baseline model was compared with recent YOLO variants and different augmentation strategies. On the test set, the model achieved a mean absolute count error of 61.3 seeds per image, a mean relative error of 12.0%, and an mAP50 of 0.18 at the locked confidence threshold of 0.15. Only 13.8% of test images had relative errors below 2%. Larger YOLO models and augmentation variants did not improve performance. These findings show that the proposed system provides approximate, non-destructive seed-count estimation under controlled imaging conditions, while highlighting the need for improved localization in dense regions and domain adaptation for fresh heads or field conditions. The annotated dataset and trained model weights are made available to support reproducible research.
Why it matches plant phenotyping methodsヒマワリ頭花の発達・不稔種子数という植物形質を、画像取得とYOLOによる推定パイプラインで定量化する手法を開発・評価しており、方法が研究の中心である。
abstractwe developed a benchtop image-based pipeline for rapid, non-destructive estimation of developed and aborted seeds on intact dried sunflower heads.
Reproduction assets foundThe authors state the source code is available on GitHub and the CVAT-annotated dataset is available via a public share link; the GitHub repository URL is explicitly provided and matches an allowed URL. The dataset link itself is not given, so only the code/checkpoint repository qualifies as an actionable public asset.Code · publicThe developed system is available as a Telegram bot [ 19 ] and the source code is available on GitHub [ 20 ]. The CVAT annotated dataset is available via a public share link.Open asset ↗lines:84-103Code / dataset availability confirmedOpenAlex · Crossref · checked 15 Sept 2026
LeafScans-Orchard is a curated, multi-year RGB image dataset of orchard plant leaves designed to support research in computer vision, machine learning, and plant phenotyping. The dataset comprises 9708 high-quality leaf scans acquired during collection campaigns conducted between 2015 and 2025, covering seven orchard crop species: apple, pear, sweet cherry, sour cherry, plum, peach, and apricot. In total, the dataset includes 67 cultivar labels. All samples were acquired using flatbed scanning under controlled conditions on a uniform background, ensuring high visual consistency and minimal background variability. The original scans were captured at 1200 dpi and subsequently converted into a public release format at 300 dpi, stored as lossless TIFF images to preserve morphological and textural details. Each image corresponds to a single leaf and is organized in a hierarchical directory structure by species, cultivar, and acquisition year, accompanied by image-level metadata and aggregated species–cultivar–year counts. LeafScans-Orchard is suitable for plant species classification, cultivar recognition, leaf morphology analysis, texture analysis, and general visual feature extraction. In addition to the main release, a representative subset of 300 original 1200 dpi scans is provided to support high-resolution analyses. The dataset is particularly suited for fine-grained classification, morphology-driven analysis, and methodological studies under controlled imaging conditions.
Why it matches plant phenotyping methods果樹葉のRGBスキャン画像を収録した公開データセットで、植物フェノタイピングおよび葉形態解析を目的とする。標準化された画像取得と再利用可能なデータ構成が中心であり、フェノタイピング用データセットとして適格。
abstractLeafScans-Orchard is a curated, multi-year RGB image dataset of orchard plant leaves designed to support research in computer vision, machine learning, and plant phenotyping.
Reproduction assets foundThe paper's core asset is the LeafScans-Orchard dataset itself (9708 RGB leaf scans, 300 dpi TIFF release plus 1200 dpi subset, image-level metadata and summary counts), openly deposited on Zenodo with an explicit DOI and CC BY 4.0 license. This is a paper-specific, public, actionable phenotyping image dataset. No codeDataset · publicthe published version of the manuscript.
Funding: This research received no external funding.
Institutional Review Board Statement: Not applicable.
Informed Consent Statement: Not applicable.
Data Availability Statement: The dataset described in this article is openly available in Zenodo
as LeafScans-Orchard Dataset (v1.0.0) at https://doi.org/10.5281/zenodo.20187966 (accessed on
10 May 2026). The repository includes the 300 dpi image release, the 1200 dpi high-resolution subset,
image-level metadata, aggregated species–cultivar–year counts, and supporting documentation. The
complete archive of original 1200 dpi scans is retained locally by the authors but is not included in
the current pubOpen asset ↗Zenodo · 10.5281/zenodo.20187966pdf-raw-page:12 lines:1-46Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
Plant leaf disease detection is a critical task in precision agriculture, where reliable diagnosis under real-world conditions is essential for reducing crop losses and supporting timely intervention. Although deep learning models have achieved high classification accuracy, their performance often degrades under domain shift between controlled laboratory datasets and real-field environments, while predictive uncertainty and confidence calibration remain largely unaddressed.This study presents an uncertainty-aware cross-domain evaluation framework based on a Hierarchical Vision Transformer (HViT) for plant leaf disease classification. The framework integrates multi-scale feature learning with Monte Carlo Dropout-based predictive uncertainty estimation and temperature-based calibration to systematically analyze model behavior in terms of accuracy, reliability, and robustness. Experiments were conducted on two complementary datasets: the New Plant Diseases Dataset (controlled conditions) and the PlantDoc dataset (field conditions), enabling bidirectional cross-domain evaluation. Results demonstrate that the proposed framework achieves superior performance, attaining 97.8% accuracy on controlled data and 93.6% on field data, while significantly improving calibration with lower Expected Calibration Error (ECE = 0.032 / 0.041), reduced Negative Log-Likelihood, and lower Brier score compared to baseline CNN and transformer models. Furthermore, the framework exhibits improved robustness under domain shift, with reduced performance degradation and stable uncertainty behavior. Overall, this study highlights the importance of integrating uncertainty estimation and calibration within a hierarchical transformer-based framework, providing a more reliable and deployment-ready solution for real-world agricultural disease diagnosis.
Why it matches plant phenotyping methods植物葉の病害状態を直接推定する不確実性-aware分類フレームワークの開発・評価が中心であり、異なる条件のデータセット間で精度、校正、頑健性を検証している。
abstractThis study presents an uncertainty-aware cross-domain evaluation framework based on a Hierarchical Vision Transformer (HViT) for plant leaf disease classification.
Reproduction assets foundThe paper's Data availability statement explicitly links the two public image datasets used for its cross-domain plant leaf disease classification experiments: the New Plant Diseases Dataset on Kaggle and the PlantDoc dataset on Dataset Ninja. No author analysis code, models, or checkpoints are reported as available.Dataset · publicThe New Plant Diseases Dataset can be obtained from Kaggle at [https://www.kaggle.com/datasets/vipoooool/new-plant-diseases-dataset]Open asset ↗Kaggle · vipoooool/new-plant-diseases-datasetlines:360-398Dataset · publicThe PlantDoc dataset is available for download at [https://datasetninja.com/plantdoc#download]Open asset ↗plantdoclines:360-398Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
PollenBB16 is an RGB pollen image dataset of Chilean flora with pixel-accurate instance segmentation masks, whose annotation was fully verified by an expert palynologist to guarantee the taxonomic reliability of every published instance. The dataset is designed to close a concrete gap in existing palynological datasets, which typically combine low taxonomic diversity, few samples per class, and low-resolution crops restricted to bounding boxes. PollenBB16 contains 16,198 brightfield optical microscopy images at the native resolution of 3088 × 2064 pixels and 36,383 pixel-accurate polygons across 16 species from the Biobío Region, spanning endemic, native and exotic species of high ecological and melliferous value such as Eucryphia glutinosa and Quillaja saponaria (endemic), Gevuina avellana and Aristotelia chilensis (native), and Medicago sativa and Brassica rapa (introduced). Each spatial position is recorded at three focal planes. The displacement along the z axis reveals features of the exine together with information on the internal structure of the grain that remain inaccessible on a single plane. From this multifocal information, more robust convolutional networks can be trained with more accurate classification. The operational quality of the dataset is backed by a leakage-safe partition that keeps the three focal planes of the same position in the same subset to avoid metric inflation, complemented by a YOLO11n-seg baseline trained for 50 epochs that reaches 0.985 mask mAP@50 on the validation set, establishing a reproducible reference point. Beyond deep learning, PollenBB16 enables interdisciplinary applications in aerobiology, biodiversity monitoring under climate change, ecological restoration of the South American temperate forest, and botanical-origin authentication of Chilean monofloral honeys.
Why it matches plant phenotyping methods植物由来の花粉粒を対象とした高解像度画像データセットとセグメンテーション基準を構築し、深層学習による画像解析を再現可能な形で検証しているため、植物フェノタイピング手法・データセットとして中心的です。
abstractPollenBB16 is an RGB pollen image dataset of Chilean flora with pixel-accurate instance segmentation masks
Reproduction assets foundThe paper's PollenBB16 pollen image dataset (16,198 multifocal RGB microscopy images with pixel-accurate instance segmentation masks) and the accompanying authors' script polygons_to_bboxes.py are publicly deposited on Zenodo (10.5281/zenodo.19830051), per the Data Availability Statement.Code · publicThe only custom code distributed with this Data Descriptor is the Python script polygons_to_bboxes.py, which regenerates the YOLO bounding-box labels in labels_bb/ from the polygon labels in labels/. The script is packaged inside the scripts/ folder of the same Zenodo repository that hosts the dataset (10.5281/zenodo.19830051) and is released under the Creative Commons Attribution 4.0 International (CC BY 4.0) license, with no restrictions on access.Open asset ↗Zenodo · 10.5281/zenodo.19830051html-lines:731-797Code / dataset availability confirmedCrossref · Europe PMC · checked 5 Sept 2026
Introduction Confidence calibration, selective prediction, out-of-distribution scoring, and deep ensembles are mature techniques in machine learning, yet their efficacy under the severe domain shift encountered when plant disease classifiers move from controlled laboratory imagery to heterogeneous field photographs has not been systematically benchmarked. Methods Models trained on PlantVillage were evaluated on PlantDoc leaf-level crop images under a parent-image-aware split protocol, and a suite of standard mitigation techniques was applied to characterize the reliability gap. Analyses included temperature scaling and selective prediction for a fine-tuned ResNet-50, quantitative image-level shift analysis, Grad-CAM visualization, simple target-aware adaptation baselines, frozen-feature backbone comparisons, and ensemble baselines. Results In the primary case study, a fine-tuned ResNet-50 suffered a 67.7-percentage-point accuracy collapse upon cross-domain transfer, while mean predicted confidence remained at 79.76%. Post-hoc temperature scaling reduced calibrated ECE to 0.3645 but left selective risk at 80% coverage at 64.30%. Quantitative image-level shift analysis confirmed large-effect-size differences in saturation ( d = 3.90), border edge density ( d = 3.33), and foreground-occupancy proxy ( d = 2.48) between the two domains, while Grad-CAM visualizations showed that the model shifts attention from lesion-centered regions in PlantVillage to background-dominated areas in PlantDoc. Simple target-aware mitigations, including adaptive batch normalization and feature moment matching, improved accuracy from 0.321 to 0.343 and 0.366, respectively, whereas DANN-style adversarial adaptation degraded performance to 0.252. A frozen-feature backbone comparison across five backbones showed that, within the energy-scoring frozen-backbone comparison, DINOv2-S/14 achieved the highest unknown-detection AUROC (0.764) and the lowest selective risk at 80% coverage (0.520), with paired Wilcoxon tests confirming statistically significant accuracy and macro-F1 differences across backbones. Two ensemble baselines were evaluated: a warm-start end-to-end ResNet-50 ensemble reduced calibrated ECE to 0.063 but achieved only 0.666 AUROC, while a lightweight DINOv2 linear-probe ensemble achieved 0.779 AUROC after calibration but under limited epistemic diversity. Discussion Neither ensemble established deployment-grade reliability: the best selective risk at 80% coverage across all configurations remained above 0.51. The principal contribution is a reproducible, deployment-oriented reliability characterization showing that standard post-hoc and lightweight adaptation techniques reduce but do not eliminate the severe reliability gap under controlled-to-field transfer in agricultural computer vision.
Why it matches plant phenotyping methods植物病害画像分類の信頼性・ドメインシフト・校正・選択的予測を体系的にベンチマークしており、病害状態を画像から推定する方法の技術評価が中心である。
abstracttheir efficacy under the severe domain shift encountered when plant disease classifiers move from controlled laboratory imagery to heterogeneous field photographs has not been systematically benchmarked.
Reproduction assets found本文中に内容が明示された植物フェノタイピング関連の補足表と、その公開リンクを確認しました。Supplement · publicSupplementary Table 1 ) was therefore constructed by normalizing all labels to a canonical Crop_Disease format and retaining only those categories for which an unambiguous semantic match existed in both datasets.Open asset ↗lines:335-337Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
Introduction Colorimetric analysis of food using the CIELab/Ch colour space (i.e., from digital images of samples) is an accessible, non-destructive method for carotenoid and anthocyanin content prediction. Literature presents very well-fit, but rudimentary, models for pigment estimation (e.g., single/multiple linear regressions). However, standardised methods that statistically account for the high multicollinearity between CIELab/Ch colour parameters, varying light conditions and colour calibration, and samples with high genotypic variability are lacking. Methods An image analysis optimisation was developed for the prediction of carotenoid and anthocyanin content of 16 carrot genotypes of different colours. Samples were photographed under six light conditions with a digital camera and image colour was calibrated before analysis with the CIELab/Ch colour space. Total pigment contents and individual carotenoid contents were analysed chemically via spectrophotometry and high-performance liquid chromatography, respectively. Partial least squares (PLS) regressions were used to assess the colour-pigment relationships to correct for high multicollinearity amongst the independent variables (CIELab/Ch colour parameters). Results/discussion The PLS models achieved satisfactory accuracy for the prediction of total carotenoid content ( ca. R 2 = 0.77) and total anthocyanin content ( ca. R 2 = 0.81) under all light conditions. The two models are suggested as robust approaches to total pigment prediction with multi-dimensional colour spaces, varying light conditions, and for a sample group of high genotypic variability. The carrot samples proved to have very high genetic diversity within each cultivar, resulting in unsatisfactory models for prediction of individual carotenoids ( ca. R 2 = 0.45) under the default light condition. However, all the results can be used to expand databases (towards artificial intelligence) and aid breeding programmes in search for higher concentrations of these interesting antioxidants for human health.
Why it matches plant phenotyping methodsニンジン試料の画像色解析を最適化し、化学分析値を用いてカロテノイド・アントシアニン含量を予測する手法を開発・検証しており、植物形質取得が研究の中心である。
abstractThe PLS models achieved satisfactory accuracy for the prediction of total carotenoid content ( ca. R 2 = 0.77) and total anthocyanin content ( ca. R 2 = 0.81) under all light conditions.
Reproduction assets foundThe authors deposited the paper's data and protocols in public repositories (DOI links in the Data availability statement). The anthocyanin quantification protocol is explicitly linked (10.34894/BTPTSV), and the other two DOIs (10.34894/P37WCL, 10.34894/OUURRH) are stated to hold the paper's data. No separate author's'Dataset · publicData and protocols are available in the following links: https://doi.org/10.34894/P37WCL , https://doi.org/10.34894/OUURRH , https://doi.org/10.34894/BTPTSV .Open asset ↗10.34894/P37WCLlines:641-686Dataset · publicData and protocols are available in the following links: https://doi.org/10.34894/P37WCL , https://doi.org/10.34894/OUURRH , https://doi.org/10.34894/BTPTSV .Open asset ↗10.34894/OUURRHlines:641-686Code / dataset availability confirmedEurope PMC · bioRxiv · checked 15 Sept 2026
Accurate and reproducible assessment of foliar disease severity is essential for evaluating the performance of heterogeneous plant communities and understanding host-pathogen interactions. However, traditional visual scoring methods remain subjective, with limited precision, and difficult to scale in large phenotyping experiments. Here, we present a semi-automated image analysis workflow designed to quantify multiple foliar disease symptoms simultaneously on wheat flag leaves sampled from varietal mixtures. The workflow combines three methodological components: (i) a standardized protocol for leaf sampling and imaging, (ii) supervised machine learning segmentation using Random Forest implemented in Ilastik to classify multiple symptoms (powdery mildew and yellow rust), and (iii) a graphical user interface facilitating pipeline deployment by non-specialist operators. To evaluate the influence of image representation on classification performance, four color spaces (RGB, HSV, HLS, LAB) were systematically compared. The approach was validated using images of durum wheat flag leaves collected from a field experiment assessing eight-way varietal mixtures under natural fungal pressure. Cross-validation against manually annotated images demonstrated high segmentation accuracy across all symptom. Comparison among color spaces revealed only minor differences in performance. Overall, this workflow offers a cost-effective, annotation-efficient and reproducible alternative to deep learning approaches, leveraging open-source and actively maintained tools while requiring limited training data and enabling objective, reproducible and scalable disease phenotyping.
Why it matches plant phenotyping methods葉の病害症状を画像解析で定量化するワークフローを開発し、色空間比較と手動アノテーションによる検証を行っており、植物表現型取得法が中心である。
abstractwe present a semi-automated image analysis workflow designed to quantify multiple foliar disease symptoms simultaneously
Reproduction assets foundThe paper's authors explicitly state that all code implementing the leaf disease quantification workflow (SegLeaf, including the graphical interface and documentation) is hosted in a public GitHub repository. No separate public phenotype dataset or trained model checkpoint is described in the supplied blocks.Code · publicted by the Agence Nationale de
la Recherche (ANR) (project SCOOP, grant no. ANR-19-CE32-0011; and project MOBIDIV,
grant no. ANR-20-PCPA-0006).
Code and Data Availability
The method and associated scripts developed in this work are freely available to the re-
search community. All code is hosted in a public GitHub repository at https://github.com/titouanlegourrierec/SegLeaf, which includes the full implementation of the method includ-
ing the graphical interface and documentation to guide users through the analysis pipeline.
15
.
CC-BY 4.0 International license
made available under a
(which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display tOpen asset ↗titouanlegourrierec/SegLeafpdf-raw-page:15 lines:1-39Code / dataset availability confirmedCrossref · checked 14 Sept 2026
Given the increasing frequency, severity, and socioecological impacts of wildfires, there is an urgent need for robust frameworks to better characterize fire behavior and flammability patterns across ecosystems to support early warning, mitigation, and management strategies. However, flammability remains difficult to quantify and scale, as it involves multiple interacting components that are typically measured at the bench scale. This study aimed to establish empirical links between spectral information, plant traits, and flammability metrics, and to scale these relationships to satellite imagery to translate these metrics into a spatial context. We combined laboratory spectroscopy, plant trait measurements including leaf mass per area, carbon, and cellulose, and combustion experiments using a simple and reproducible burning device. In total, 84 samples were collected and analysed, allowing us to characterise how spectral signatures relate to vegetation traits and fire behaviour. Spectral indices were developed to estimate plant traits, which were subsequently used as predictors in flammability models. These models were then transferred to Environmental Mapping and Analysis Program (EnMAP) hyperspectral imagery to derive spatial estimates across eucalypt forests and grasslands of the Australian Capital Territory (ACT). Spectral information distinguished fuel types and captured variability of the plant traits, while these traits showed associations with combustion behaviour. Based on these links, the best-performing model predicted the rate of temperature increase, a combustibility metric, in eucalypt forests (R2 = 0.70; Root Mean Square Error = 32.48 °C/s). In contrast, grassland models showed limited predictive performance, likely due to weaker relationships between plant traits and flammability metrics. Overall, this study demonstrates a practical and scalable approach for deriving flammability maps from hyperspectral and in situ data, highlighting the potential of plant-trait-based remote sensing. The resulting maps should not be interpreted as standalone fire risk products, but rather as a characterization of the structural and biochemical drivers of flammability. The main constraint of this work is the limited sample size. Future research should expand spatial and temporal coverage to better capture vegetation variability and enable the inclusion of independent validation datasets. Exploring alternative combustion protocols and testing more advanced spectral modelling approaches for trait estimation would provide additional insights.
Why it matches plant phenotyping methods植物形質を分光情報から推定し、ハイパースペクトル画像へ展開して可燃性関連の植物状態を評価する手法が研究の中心であり、モデル性能も検証しているため。
abstractSpectral indices were developed to estimate plant traits, which were subsequently used as predictors in flammability models.
Reproduction assets foundThe paper's supplementary materials (hosted publicly by MDPI) contain the paper-specific plant phenotype measurements: sampled species lists, fractional cover, and measured vegetation traits across dates and plots, plus combustion replicate variability and trait–flammability relationship data. The raw underlying data,谱Supplement · publicbroader environmental coverage, improved plant trait retrieval meth-
ods, and independent validation. Future work should also explore non-linear modelling
frameworks to better capture the complexity of vegetation flammability across ecosystems.
Supplementary Materials: The following supporting information can be downloaded at:
https://www.mdpi.com/article/10.3390/rs18101546/s1, Supplementary Table S1 provides the list of
sampled plant species and their percentage cover across sites, paddocks, plots, and fuel types; Table
S2 presents the fractional cover of each species and litter component; Figure S1 shows the study-site
vegetation map; Figures S2–S6 show the measured vegetation traits acrosOpen asset ↗pdf-raw-page:22 lines:1-49Code / dataset availability confirmedCrossref · checked 15 Sept 2026
Plant disease is a serious threat to agricultural productivity and food security worldwide. Traditional diagnostic methods such as manual observation and laboratory testing are time-consuming, labor-intensive and error prone. The emergence of artificial intelligence (AI) and deep learning (DL) offer scalable solutions for precision agriculture in plant disease detection using advanced computational techniques to process large datasets. Hybrid deep learning architecture integrates Convolutional Neural Networks (CNNs) along with Artificial Neural Networks (ANNs) can leverage both visual and contextual data to improve detection performance. The hybrid CNN-ANN model was developed to analyze visual data (plant images) and contextual data (environmental and soil metrics). The CNN module extracted spatial and textural features from plant images, while the ANN module processed environmental parameters. These outputs were fused into a unified feature vector for disease classification. A total of 15 plant species and their associated diseases were analyzed using 200-270 training samples and 150-190 testing samples for each disease across a total of 1000 images. The model was judged by metrics such as detection accuracy, AUC, sensitivity etc. Data augmentation, pre-trained architectures (e.g., ResNet50) and early stopping techniques were utilized to improvise model performance. The hybrid model saliently achieved detection accuracy consistently above 87% with majority of diseases surpassing 90%. Highperforming cases like Rice Blast (92.5%), Tomato Early Blight (93.8%), and Coffee Rust (93.0%), with AUC values of 0.93 or higher, sensitivity exceeding 94% and specifically above 90%. Diseases of Sugarcane Red Rot and Tea Blister Blight exhibited sensitivities of 92.4% and 92.1% and specificities of 91.1% and 90.5% respectively. Moderate accuracy for Coconut Bud Rot (87.5%) and Mustard Alternaria Blight (87.8%) was due to smaller training sample sizes.
Why it matches plant phenotyping methods植物画像から病害状態を分類するハイブリッドCNN-ANN手法を開発し、精度・AUC・感度などで評価しており、病害フェノタイピング手法が研究の中心である。
abstractThe hybrid CNN-ANN model was developed to analyze visual data (plant images) and contextual data (environmental and soil metrics).
Reproduction assets foundThe paper's plant disease detection model was trained on public plant image datasets: the PlantSeg dataset (Zenodo record 13958858, DOI 10.5281/zenodo.13293891) and the UCI Machine Learning Repository Plants dataset. Both are cited in Materials and Methods as sources of the visual data used for the CNN module. No code,Dataset · publicebao (ZiranKexueBan)/Journal of
Huazhong University of Science and Technology
(Natural Science Edition). 2021;49(8).
37. Ma C, Mu X, Sha D. Multi-Layers Feature Fusion of
Convolutional Neural Network for Scene
Classification of Remote Sensing. IEEE Access.
2019;7.
38. Hämäläinen W.Plants Dataset[Internet]. 2024.
Available from:
https://archive.ics.uci.edu/dataset/180/plants
39. WeiT. PlantSeg: A Large-Scale In-the-wild Dataset
for Plant Disease Segmentation [Internet]. 2018.
Available from: https://zenodo.org/records/13958858Open asset ↗180pdf-raw-page:15 lines:1-48Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Abstract Ustilago maydis is a biotrophic fungus that causes smut disease in maize, leading to tumor formation on aerial parts of the plant. While U. maydis has been a model for plant-fungal interaction studies, no tool has existed to automatically quantify infection symptoms under laboratory conditions for deep learning analysis. To address this, we developed a rotating camera system that captures videos of plants under customized lighting and shutter settings. These videos were used to train machine learning models to distinguish between healthy and infected plants. Two machine learning models have been presented. In the first approach, by employing a naive masking technique and combining classical machine learning with deep learning classifiers, the model achieved a reasonable performance, with an Area Under the Curve (AUC) of 0.90 on the Receiver Operating Characteristic (ROC), displaying high sensitivity and specificity. The second approach utilizes pre-trained YOLO11 model for object detection and further classification. The YOLO11-based approach outperforms traditional methods, achieving near-perfect accuracy (AUC: 0.99-1.00), demonstrating its superiority for real-time, scalable applications. Our toolset, featuring a cost-efficient and customizable scanning platform with open building-blocks design, provides a valuable resource for unbiased disease symptom detection and scoring, with potential applications in other plant pathology studies. This point enables easy replication and adaptation by other research laboratories which makes the platform robust, scalable and practical beyond our specific application.
Why it matches plant phenotyping methods植物の感染症状を画像から自動検出・定量する低コスト撮像プラットフォームと解析モデルを開発しており、植物表現型取得法が中心的である。
abstractwe developed a rotating camera system that captures videos of plants under customized lighting and shutter settings.
Abstract Current phytopathological diagnostic systems rely on manual inspections or laboratory analyses, which delay early detection and limit in-field responsiveness. Phytopathogenic fungal diseases pose a persistent threat to food security, directly affecting the productivity of essential crops such as potato ( Solanum tuberosum ) and tomato ( Solanum lycopersicum ) [1]–[5]. Among these diseases, Phytophthora infestans , the causal agent of late blight, is characterized by its high virulence and rapid spread, capable of generating significant losses in short periods when detection occurs too late [3], [4]. To address this issue, a computer vision and deep learning–based system for multistage detection of fungal infections in potato and tomato crops is proposed. The system comprises a convolutional neural network optimized for edge processing and a mobile robotic platform equipped with a manipulator arm for localized treatment application. The developed model was deployed on a Raspberry Pi 4 connected to a 12-MP Raspberry Pi Camera Module 3 NoIR, responsible for acquiring RGB images in the field. The proposed network was compared with reference architectures—ResNet-50, VGG16, MobileNetV2, and Inception-v3—within a four-stage detection pipeline: crop identification, health-state classification, infection diagnosis, and foliar severity estimation. A dataset of 18,200 images obtained from publicly accessible online sources, under diverse lighting and background conditions, was used, partitioned into 70% for training, 20% for validation, and 10% for testing. Preliminary results show an average accuracy in the range of 0.90–0.92, with inference latencies below 60 ms per image, ensuring smooth performance on the Raspberry Pi 4 without requiring cloud connectivity. Additionally, the network demonstrated higher sensitivity to visual variations compared to the baseline models.
Why it matches plant phenotyping methods植物病害の健康状態・感染・葉面重症度を画像から推定するコンピュータビジョン手法を開発・比較検証しており、植物表現型取得が中心である。
abstracta computer vision and deep learning–based system for multistage detection of fungal infections in potato and tomato crops is proposed
Reproduction assets foundThe paper's CNN training data are two publicly available third-party plant-disease image datasets (Mendeley Data and Kaggle Plant Village) with explicit URLs in the Data Availability Statement. The authors' field-test images and experimental records are only available on request, and no analysis code or trained model/сDataset · public10
Network, DOI: 10.17632/tywbtsjrjv.1, available at
https://data.mendeley.com/datasets/tywbtsjrjv/1, and the
Kaggle Plant Village dataset, available at
https://www.kaggle.com/datasets/emmarex/plantdisease.The field-test images and experimental records generated during
the current study during the real-world evaluation of the
embedded-vision system are available from the corresponding
author on reasonable request.
IX. REFERENCOpen asset ↗10.17632/tywbtsjrjv.1pdf-raw-page:11 lines:1-98Dataset · public10
Network, DOI: 10.17632/tywbtsjrjv.1, available at
https://data.mendeley.com/datasets/tywbtsjrjv/1, and the
Kaggle Plant Village dataset, available at
https://www.kaggle.com/datasets/emmarex/plantdisease.The field-test images and experimental records generated during
the current study during the real-world evaluation of the
embedded-vision system are available from the corresponding
author on reasonable request.
IX. REFERENCES
[1] P. W. Crous, A. Y. Rossman, M. C. Aime, W. C. Allen, T.
Burgess, J. Z. Groenewald y L. A. CastlebuOpen asset ↗Kagglepdf-raw-page:11 lines:1-98Code / dataset availability confirmedOpenAlex · checked 15 Sept 2026
ABSTRACT 3D reconstruction has matured into a robust technology. However, small, flexible objects such as conifer seedlings remain challenging due to their fine‐scale structures, and susceptibility to movement. This study investigates and evaluates methods for reconstructing spruce ( Picea abies ) and pine ( Pinus sylvestris ) seedlings, with the aim of establishing a workflow capable of capturing geometry and texture for applications in machine learning and virtual testing environments. Two acquisition approaches were tested: photogrammetry using a RGB camera and a 3D scanner, both mounted on a robotic arm. While the scanner produced incomplete results, the photogrammetry approach successfully generated point clouds (pcl) with color information. Three different photogrammetry software were tested before relying on Agisoft Metashape and Meshroom for image processing and dense pcl generation, followed by pcl filtering in CloudCompare and meshing in Blender. Six seedlings were reconstructed to textured meshes and quantitatively evaluated using the metrics precision, recall, F1‐score, mask intersection‐over‐union (IoU), and boundary IoU. Results showed an average mask IoU of 75.7% and F1‐score of 86.1%. Pine seedlings yielded higher recall and F1‐scores, whereas spruce reconstructions demonstrated higher precision. The proposed semi‐automated workflow demonstrates the feasibility of reconstructing small and slender structured flexible objects, specifically conifer seedlings.
Why it matches plant phenotyping methods針葉樹苗の形状・テクスチャを取得する3D画像再構成ワークフローを開発・比較・定量評価しており、植物フェノタイピング手法が中心である。
abstractThis study investigates and evaluates methods for reconstructing spruce ( Picea abies ) and pine ( Pinus sylvestris ) seedlings, with the aim of establishing a workflow capable of capturing geometry and texture for applications in machine learning and virtual testing environments.
Reproduction assets foundThe paper's Data Availability Statement states that the raw seedling image data and finalized textured meshes (the paper's phenotyping/3D reconstruction inputs and outputs) are freely available on Zenodo under DOI 10.5281/zenodo.19823955, which appears in the allowed URL list.Dataset · publicand without adjusting the scanning parameters, while also re-
Data Availability Statement
taining texture and color. In contrast to prior approaches that
require manual intervention or do not preserve visual informa- Raw image data and finalized textured meshes are freely available at
Zenodo.org with https://doi.org/10.5281/zenodo.19823955.
tion, the proposed workflow enables a semi-automated recon-
struction process suitable for dataset generation. As shown, the
methodology is effective for the digital reconstruction of small References
and slender structured flexible objects and holds potential for
Abbood, S. A., H. A. Ajjah, A. H. H. Alboabidallah, M. U. MohaOpen asset ↗Zenodopdf-layout-page:14 lines:50-74Code / dataset availability confirmedOpenAlex · Crossref · Europe PMC · checked 5 Sept 2026
Precision greenhouse agriculture enhances plant health and crop yields by continuously monitoring key plant parameters. Stem diameter is such a parameter and is monitored to support decisions on plant care. However, traditional contact-based methods induce thigmomorphogenic effects that impact plant growth. Here, we introduce the Optical Caliper (OC), a novel contactless device for precise, non-invasive stem diameter measurement. The OC operates by projecting a collimated light beam to cast a shadow of the stem onto a high-resolution image sensor. The shadow size is a measure for the stem diameter. Controlled laboratory tests show the OC offers an accuracy comparable to that of a Digital Caliper (DC). Field trials on irregular tomato and cucumber stems demonstrate a repeatability of 0.1-0.2 mm. The OC's non-invasive design and high repeatability exceed the performance of a DC, making it particularly suited for accurately monitoring soft, variable plant structures. Bringing the advantage of avoiding thigmomophogenic effects and thus optimizing crop yield, the OC is a promising tool for high-throughput plant phenotyping and precision agriculture applications.
Why it matches plant phenotyping methods植物の茎径を非接触・高精度に測定する光学デバイスを開発し、実験室および圃場で精度・再現性を検証しており、植物表現型取得法が研究の中心です。
abstractHere, we introduce the Optical Caliper (OC), a novel contactless device for precise, non-invasive stem diameter measurement.
Reproduction assets foundThe paper's measurement data (optical caliper, digital caliper, and micrometer readings on reference cylinders and tomato/cucumber stems) is openly deposited on the SURF data repository of The Hague University of Applied Sciences. No author analysis code or trained models are explicitly deposited; other allowed URLs (DDataset · publicThe data gathered during this study is openly available via https://hhs.data.surf.nl/s/nqnFYBf42KPA75P (accessed on 10 February 2026).Open asset ↗hhs.data.surf.nlhtml-lines:282-314Code / dataset availability confirmedCrossref · checked 5 Sept 2026
Abstract Background Apoplastic pH is a central regulator of plant growth, development, and environmental adaptation, influencing cell expansion, nutrient uptake, and extracellular signaling. Many studies have successfully used HPTS to monitor relative changes in apoplastic pH in plants. At the same time, research increasingly targets pH-dependent biochemical and biophysical processes. Many enzymatic activities, ion binding events, and receptor–ligand interactions depend on defined proton concentrations. Accordingly, the development of reliable approaches to measure absolute pH in living tissues is gaining importance. Methods A calibration-based workflow was developed to enable quantitative assessment of absolute apoplastic pH using ratiometric HPTS imaging. The approach integrates a simplified two-point normalization strategy with an in-vitro derived sigmoidal calibration model, thereby minimizing the need for extensive in-vivo calibration curves. Confocal imaging was performed using HPTS excited at two wavelengths followed by ratiometric image processing. Data analysis is supported by a custom Fiji plugin, Ratio2pH, which converts ratiometric images into pixel-resolved maps of absolute pH. Results In vitro characterization revealed a robust, non-linear relationship between normalized HPTS ratios and pH, enabling accurate pH estimation within the physiologically relevant range of pH 5.0–7.0. When applied in-vivo to Arabidopsis thaliana roots, the workflow yielded extracellular pH estimates consistent with the pH of the incubation medium and detected reproducible pH shifts in response to pharmacological treatments. Conclusions This workflow enables reproducible, spatially resolved measurement of absolute apoplastic pH in living plant tissues. By combining a simplified calibration strategy with accessible image analysis tools, it facilitates quantitative extracellular pH measurements and their integration into biochemical and biophysical analyses.
Why it matches plant phenotyping methods生きた植物組織の絶対アポプラストpHを画像から定量する校正ワークフローを開発・検証し、Fijiプラグインも提供しているため、植物状態の取得法が中心である。
abstractA calibration-based workflow was developed to enable quantitative assessment of absolute apoplastic pH using ratiometric HPTS imaging.
Reproduction assets foundThe paper deposits its authors' analysis code and data publicly: the Ratio2pH Fiji plugin (Zenodo 10.5281/zenodo.15599805), a Python script for sigmoidal calibration curve fitting (Zenodo 10.5281/zenodo.17303477), and source data files and raw confocal images (Freidata 10.60493/t29wb-7my86). The Zenodo 15658668 ratiom�Code · publicThe Python Script for generating a user-defined sigmoidal calibration curve is available at Zenodo: https://doi.org/10.5281/zenodo.17303477Open asset ↗Zenodo · 10.5281/zenodo.17303477lines:175-235Dataset · publicSource data files and raw images are uploaded at Freidata, the data server of the University of Freiburg, available under https://doi.org/10.60493/t29wb-7my86Open asset ↗Freidata · 10.60493/t29wb-7my86lines:175-235Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
Plants defend against pathogens such as fungi by initiating coordinated structural and chemical responses. Pathogen perception triggers rapid cytosolic calcium influx and calcium oscillations that drive defense gene expression, yet the mechanisms by which these signals encode stressor intensity and propagate systematically remain unclear. Here, we present a microfluidic system to characterize intracellular calcium dynamics in protonemal colonies of the moss Physcomitrium patens (Hedw.) upon precise and reversible exposure to fungal chitin oligosaccharides. Epifluorescent imaging of cells expressing the calcium indicator GCaMP6f revealed a rapid, coordinated calcium response to chitin addition, followed by stereotyped oscillations that subsided quickly upon stimulus removal. We implemented an unbiased image segmentation algorithm using pixel-based k -means clustering to automatically locate regions with specific oscillatory signatures. Calcium dynamics were distinct across adjacent cells, distinguishable by cell type, and significantly modulated by circadian rhythm, adaptation time within the device, and stimulus timing. Cytosolic calcium oscillations, which rose and fell symmetrically within about 60 s, occurred spontaneously during the subjective night and following short adaptation periods. Chitin elicited strong oscillations with increased frequency, amplitude, and duration, and repeated pulses entrained regular, colony-wide oscillations at the stimulation interval. This study complements prior investigations of whole plant and growth tip dynamics and provides a quantitative framework to study calcium signaling in plants, including mechanisms of signal propagation and the role of oscillation frequency on gene expression.
Why it matches plant phenotyping methods植物細胞のカルシウム動態を定量するマイクロ流体・蛍光イメージング系と自動画像セグメンテーションを開発し、植物の生理状態を抽出する方法が研究の中心である。
abstractHere, we present a microfluidic system to characterize intracellular calcium dynamics in protonemal colonies of the moss Physcomitrium patens
Reproduction assets foundThe paper's Data Availability Statement explicitly makes analysis scripts and sample data publicly available on the authors' GitHub repository (albrechtLab/moss_calcium), and the MDPI supplementary materials (plants-15-00582-s001.zip) contain the paper's timelapse calcium-imaging videos and supplementary figures. Raw/全Code · publicData are available upon request. Analysis scripts and sample data are publicly available at https://github.com/albrechtLab/moss_calcium (accessed on 1 January 2026).Open asset ↗albrechtLab/moss_calciumlines:188-251Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
Soybean ( Glycine max L. ) performs an important position as a main resource of protein in Indonesia. Its quality and productivity can be assessed based on the characteristics of its seed. Accordingly, the identification process through the observation of soybean seed traits is a crucial step in plant breeding and quality assurance. Manual approaches rely on manual observation, which is subjective, prone to human error and time-consuming. With the improvement of artificial intelligence, automated seed identification has appeared as a potential solution. However, progress is constrained by the lack of open and standardized image datasets, especially for locally bred varieties in developing countries. To address this gap, we propose an open image dataset of Indonesian soybean seeds from three widely cultivated and plant-bred varieties: Anjasmoro, Grobogan, and DEGA-1. The dataset consists of high-resolution seed images captured with an Epson L360 flatbed scanner, with the optical resolution fixed at 800 dots per inch, yielding images of 6800 × 9359 pixels. All raw images are saved in JPG format. No manually segmentation masks are released in this version, instead of using Deeplab V3+ with MobileNet as backbone to enable the automated seed image segmentation. The curated dataset is intended to support a broad range of applications, including computer vision tasks such as image classification and segmentation, as well as research in plant breeding, seed quality assessment, and agricultural informatics. By providing a standardized and publicly accessible resource, this dataset contributes to the advancement of interdisciplinary studies at the intersection of agriculture and artificial intelligence.
Why it matches plant phenotyping methods大豆種子画像を標準化して公開するデータセット研究であり、種子形質の自動画像解析・セグメンテーションを支援する方法論的資源が中心です。
titleAn open image dataset of Indonesian soybean seed varieties (Anjasmoro, Grobogan, DEGA-1) for agricultural research and machine learning applications.
Reproduction assets foundThe paper is a data descriptor for a public Mendeley Data repository containing the authors' own soybean seed image dataset (raw scans and segmented seed images) used for seed phenotyping, with an explicit direct URL and DOI.Dataset · publicData accessibility
Repository name: Mendeley Data
Data identification number: DOI: 10.17632/c733bjz4m3.3
Direct URL to data: https://data.mendeley.com/datasets/c733bjz4m3/3Open asset ↗Mendeley Data · 10.17632/c733bjz4m3.3html-lines:115-142Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
The rapid and precise identification of apple leaf diseases is crucial for minimizing yield loss in precision agriculture. However, many existing deep learning methods struggle to be applicable in real-world settings, are not easily interpretable, and often lack sufficient statistical validation. To address these difficulties, we propose our solution approach LeafSightX . This dual-backbone architecture combines features from DenseNet201 and InceptionV3 using Multi-Head Self-Attention (MHSA) techniques, enhancing representational capability and spatial context reasoning. Our extensive procedure includes specialized preprocessing and limited data augmentation, improving model resilience in many scenarios. Furthermore, LeafSightX integrates explainable AI techniques with Grad-CAM visualizations to improve transparency. In assessments of a five-class apple leaf disease dataset featuring field and laboratory images, LeafSightX demonstrates exceptional performance, attaining a test accuracy of 99.64%, an F1-score of 0.9962, and AUC and PR-AUC scores of 1.000, far surpassing all baseline CNNs. Cross-validated Cohen's Kappa (mean = 0.9917, σ = 0.0020) and AUC (mean = 0.9998) indicate a significant level of predictive consistency. Despite its architectural complexity, the model offers real-time inference capabilities, ensuring per-sample latency suitable for edge device deployment. Additionally, the proposed LeafSightX framework was trained and evaluated on an additional independent apple leaf disease dataset, achieving a test accuracy of 99.69%, demonstrating its robustness and generalization. Our approach is a rigorously evaluated, clear, and highly accurate system for identifying plant diseases, providing a reproducible foundation for the actual application of AI in agriculture.
Why it matches plant phenotyping methodsリンゴ葉の病害状態を画像から識別するCNN手法を開発し、複数データセット・交差検証・ベースライン比較で性能を評価しており、植物病害表現型の取得・推定が中心である。
Reproduction assets foundThe paper uses two public Kaggle apple leaf disease image datasets as its phenotyping inputs; both are directly cited with public URLs. No author analysis code, trained model checkpoints, or supplementary code repository is deposited — the data availability statement only offers contact with corresponding authors.Dataset · publicThis research utilizes the Apple Tree Leaf Disease dataset, collected from Kaggle and made available by Nirmal (Kaggle, 2025).Open asset ↗Kagglehtml-lines:128-184Dataset · publicDhar S. (2023). Apple leaf disease classification dataset. Available online at: https://www.kaggle.com/datasets/showravdhar/apple-disease-dataset (Accessed November 1, 2023).Open asset ↗Kaggle · showravdhar/apple-disease-datasethtml-lines:1449-1484Code / dataset availability confirmedEurope PMC · bioRxiv · checked 14 Sept 2026
Quinoa ( Chenopodium quinoa Willd.) is a genetically diverse Andean crop valued for its nutrition and adaptability to varied agro-climatic conditions with potential for cultivation in European and Mediterranean, particularly on marginal lands. Low temperatures during early sowing can impair germination, while delayed sowing increases the risk of poor maturation due to unfavorable autumn weather. To assess the adaptation of quinoa to low temperature conditions, that reflect cold stress, we evaluated germination and phenotypic variation in 60 accessions from highland and coastal ecotypes across three sowing dates in South-Western Germany: late winter (S1), early spring (S2), and spring (S3). Early sowing under low temperature conditions in S1 delayed seedling-emergence and reduced emergence percentages, yet these plants produced the highest average seed yield per plot (64 g) compared to S2 (46 g) and S3 (35 g). Highland accessions showed earlier seedling-emergence and with higher emergence percentages, while coastal types matured earlier and gave higher yields across sowing dates. A complementary laboratory experiment assessed germination under cold (4.4 °C) and control (18.3 °C) conditions, using both manual scoring and image analysis via a Mask R Convolutional Neural Network, to track seedling growth. This confirmed the beneficial germination performance of highland accessions under low temperature conditions, with strong agreement between manual and automated scoring. Our findings suggest that quinoa demonstrates resilience to cold stress with highland quinoa exhibiting superior germination traits, and early sowing, despite reduced emergence, can lead to higher yields. We conclude that combining favorable traits such as faster maturity and higher yield of coastal ecotypes with superior germination traits of highland accessions is a promising avenue for breeding improved quinoa varieties for cold climatic regions.
Why it matches plant phenotyping methodsMask R-CNNによる発芽・幼植物成長の画像解析を手動評価と比較し、強い一致を検証しており、植物表現型取得法の技術的検証を含む。
abstractA complementary laboratory experiment assessed germination under cold (4.4 °C) and control (18.3 °C) conditions, using both manual scoring and image analysis via a Mask R Convolutional Neural Network, to track seedling growth.
Reproduction assets foundThe paper states that all phenotypic data and R analysis scripts are available as supplementary material (publicly hosted with the bioRxiv preprint), while raw seed germination images are only available upon request. No separate repository or trained model checkpoint is named.Dataset · publicData availability: All phenotypic data and R scripts used for the analysis are available
as supplementary material.Open asset ↗pdf-page:1 lines:1-52Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
Background The plant vacuole arises by orchestrated interplay of membrane trafficking, cytoskeletal rearrangements and a variety of signaling pathways. In the root, the characteristic large central vacuole develops by endomembrane reorganization occurring mainly in the transition zone. The vacuole's bounding membrane-the tonoplast-can be visualized in vivo using fluorescent protein markers, allowing for quantitative analysis of confocal microscopy images. Tonoplast organization can thus serve as a sensitive indicator of changes to any of the processes involved in vacuole biogenesis. The Vacuolar Morphology Index (VMI) is widely accepted as a quantitative measure of vacuole structure. However, this metric has two drawbacks-it only reflects the size of the largest vacuolar compartment (missing therefore possible differences in the organization of smaller compartments), and its determination is labor intensive, limiting its use on large datasets. Results We developed an alternative metric for describing vacuole organization, named the Tonoplast Topology Index (TTI), which overcomes the above-mentioned shortcomings of the VMI. We compared the performance of our protocol with VMI on a simulated dataset and on real data. To validate the methods´ performance, we used it to confirm the previously reported differences in vacuole shape and size between Arabidopsis thaliana roots grown on the surface of an agar medium compared to those embedded inside the agar. Both VMI and TTI could efficiently detect the relatively subtle changes in vacuole organization depending on the position of the root in the agar, and provided correlated results. However, only TTI produced data with close to normal value distribution, simplifying subsequent statistical evaluation. Conclusions We present the protocol for TTI determination as a two-stage semi-automated procedure involving microscopic image analysis employing an ImageJ macro and subsequent processing of numeric data in the Jupyter Notebook environment, together with benchmarking image data. Since this implementation is freeware-based, platform-independent and (relatively) user-friendly, we hope it will find its use as a high throughput, added value alternative to the VMI metric.
Why it matches plant phenotyping methods植物液胞構造を定量化する新規指標と半自動画像解析プロトコルを開発し、シミュレーションおよび実画像で既存指標と比較・検証しているため、植物フェノタイピング手法が中心である。
abstractWe developed an alternative metric for describing vacuole organization, named the Tonoplast Topology Index (TTI)
Reproduction assets foundThe paper deposits its benchmark confocal image dataset in the EMBL-EBI BioImage Archive (S-BIAD2226) and its TTI analysis software (ImageJ macro and Jupyter/Python scripts) on GitHub, both with explicit public availability statements.Dataset · publicImage data generated and analyzed in the current study are available in the EMBL-EBI BioImage Archive repository, accession number S-BIAD2226Open asset ↗EMBL-EBI BioImage Archive · S-BIAD2226lines:141-163Code · publicArchive copy, additional sample data and possible future updates of the software tool generated here are also available at [ https://github.com/GeorgeCaldarescu/TTI-Tonoplast-Topology-Index ] .Open asset ↗GitHub · GeorgeCaldarescu/TTI-Tonoplast-Topology-Indexlines:141-163Code / dataset availability confirmedOpenAlex · arXiv · checked 13 Sept 2026
Semantic reconstruction of agricultural scenes plays a vital role in tasks such as phenotyping and yield estimation. However, traditional approaches based on manual scanning or fixed camera setups remain a major bottleneck, while active-mapping methods based solely on occupancy grids are too coarse for accurate trait estimation. To address this gap, we propose an active 3D reconstruction framework for horticultural environments using a mobile manipulator. The system integrates OctoMap with 3D Gaussian Splatting to enable accurate and efficient target-aware mapping. A low-resolution OctoMap provides probabilistic occupancy information for informative viewpoint selection and collision-free planning, while 3D Gaussian Splatting leverages geometric, photometric, and semantic information to optimize 3D Gaussians for high-fidelity scene reconstruction. We further introduce a robust mapping strategy that mitigates semantic segmentation and depth noise, together with a background pruning method that reduces memory and computational cost. We validate our framework across simulated, laboratory, and real greenhouse scenes, showing consistent improvements across three state-of-the-art Gaussian Splatting backbones. In simulation, where ground-truth geometry is available, our approach outperforms occupancy-based mapping in both reconstruction accuracy and runtime efficiency: compared with a 0.01m-resolution OctoMap, it doubles the fruit-level F1 score under noisy conditions while achieving up to a threefold reduction in runtime. Beyond simulation, novel-view synthesis quality also improves consistently in laboratory and real greenhouse environments, with PSNR and mIoU improving by up to 1.5 dB and 18%, respectively. Finally, the reconstructed semantic maps enable fruit counting and volume estimation with accuracies approaching 80%.
Why it matches plant phenotyping methods園芸ロボット向けの3D再構成・能動マッピング手法を開発し、果実の計数・体積推定という植物形質の取得に適用・検証しているため、フェノタイピング手法が中心的です。
titleOctoSplat: Hybrid OctoMap-Gaussian Splatting for Active Semantic Mapping and Phenotyping with Horticultural Robots
Reproduction assets foundThe paper's supplementary material is hosted on the authors' public project page (jrcuaranv.github.io/octosplat), and the authors state that all code and data are publicly available. The SimSense repository is a third-party depth-sensor simulator tool, not a paper-specific asset.Code · publicAll code and data are publicly available to facilitate reproducibility.Open asset ↗lines:59-163Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
This study employed an HY-6010-S hyperspectral imaging system, covering a spectral range of 400-1000 nm, combined with an RGB industrial camera to acquire multimodal data. The dataset simulates phenotypic analysis scenarios of maize seeds under controlled laboratory conditions, with the ambient temperature maintained at 20-25°C. Comprehensive testing was conducted using 12 different maize varieties. Approximately 200 seed samples were collected per variety, resulting in a total sample size of about 2400, each subjected to hyperspectral and RGB image acquisition. Preprocessing steps included noise reduction, background removal, band selection, and modality alignment. To ensure the accuracy and reliability of the experimental data, HHIT software and Python were utilized for data processing. This dataset plays a significant role in seed variety classification, phenotypic analysis, precision agriculture, and machine learning applications.
Why it matches plant phenotyping methodsトウモロコシ種子のマルチモーダル画像を収集・前処理した再利用可能なデータセットであり、種子の表現型解析を主要目的としているため、フェノタイピング手法・データセット研究に該当する。
abstractThis study employed an HY-6010-S hyperspectral imaging system, covering a spectral range of 400-1000 nm, combined with an RGB industrial camera to acquire multimodal data.
Reproduction assets foundThe paper is a Data in Brief article depositing its own multimodal maize seed hyperspectral and RGB image dataset (2400 seeds, 12 varieties) on Mendeley Data, with a direct public URL and DOI given in the article.Dataset · publicRepository name: Mendeley Data
Data identification number: doi: 10.17632/4n4xbnx8sr.1
Direct URL to data: https://data.mendeley.com/datasets/4n4xbnx8sr/1Open asset ↗Mendeley Data · 10.17632/4n4xbnx8sr.1html-lines:1-110Code / dataset availability confirmedEurope PMC · OpenAlex · Crossref · checked 15 Sept 2026
Background Root hairs play a key role in plant nutrient and water uptake. Historically, root hair traits have largely been quantified manually. As such, this process has been laborious and low-throughput. However, given their importance for plant health and development, high-throughput quantification of root hair morphology could help underpin rapid advances in the genetic understanding of these traits. With recent increases in the accessibility and availability of artificial intelligence (AI) and machine learning techniques, the development of tools to automate plant phenotyping processes has been greatly accelerated. Results We present pyRootHair, a high-throughput, AI-powered software application to automate root hair trait extraction from microscope images of plant roots grown on agar plates. pyRootHair is capable of batch processing over 600 images per hour without manual input from the end user. In this study, we deploy pyRootHair on a panel of 24 diverse wheat (Triticum aestivum and Triticum turgidum ssp. durum) cultivars and uncover a large, previously unresolved amount of variation in many root hair traits. We show that the overall root hair profile falls under 2 distinct shape categories and that different root hair traits often correlate with each other. We also demonstrate that pyRootHair can be deployed on a range of plant species, including oat (Avena sativa), rice (Oryza sativa), teff (Eragrostis tef), and tomato (Solanum lycopersicum). Conclusions The application of pyRootHair enables users to rapidly screen a large number of plant germplasm resources for variation in root hair morphology, supporting high-resolution measurements and high-throughput data analysis. This facilitates downstream investigation of the impacts of root hair genetic control and morphological variation on plant performance. pyRootHair is installable via PyPI (https://pypi.org/project/pyRootHair/) and can be accessed on GitHub at https://github.com/iantsang779/pyRootHair.
Why it matches plant phenotyping methods植物根毛形態を顕微鏡画像から自動抽出するAIソフトウェアを開発し、複数作物で適用・実証しており、表現型取得手法が研究の中心である。
abstractWe present pyRootHair, a high-throughput, AI-powered software application to automate root hair trait extraction from microscope images of plant roots grown on agar plates.
Reproduction assets foundThe paper's root hair phenotyping software (pyRootHair) is publicly available on GitHub and PyPI, the data and notebooks used to generate the manuscript figures are deposited in the repository's paper_data folder, and the software is annotated in the DOME-ML registry. The GigaDB deposit (10.5524/102771) is referenced,但Code · publicregression lines were computed using statsmodels (v0.14.4). Scikit-learn (v.1.5.2) was used for quality control of segmented images. nnU-Netv2 (v2.5.1) was used to create the image segmentation model with PyTorch (v.2.5.1) and CUDA (v.12.6).
Availability of Source Code and Requirements
Project name: pyRootHair
Project homepage: https://github.com/iantsang779/pyRootHair
Operating system(s): Linux, MacOS, Windows
Programming language: Python
License: MIT License
Supplementary Material
giaf141_Supplemental_File giaf141_Authors_Response_To_Reviewer_Comments_Original_Submission giaf141_GIGA-D-25-00279_Original_Submission giaf141_GIGA-D-25-00279_Revision_1 giaf141_Reviewer_1_Report_Original_SubmisOpen asset ↗github.com/iantsang779/pyRootHairlines:250-287Dataset · publicThe source jupyter notebook and data used to generate all figures in the manuscript have been deposited on GitHub [ 39 ].Open asset ↗lines:400-405Code · publiclarge number of plant germplasm resources for variation in root hair morphology, supporting high-resolution measurements and high-throughput data analysis. This facilitates downstream investigation of the impacts of root hair genetic control and morphological variation on plant performance. pyRootHair is installable via PyPI ( https://pypi.org/project/pyRootHair/ ) and can be accessed on GitHub at https://github.com/iantsang779/pyRootHair .
Keywords: root hairs, plant phenotyping, machine learning, computer vision, AI, U-Net, wheat, roots, software
status released display-pdf yes is-olf no is-manuscript no is-preprint no is-journal-matter no is-scanned no is-retracted no
Received 2025 JOpen asset ↗lines:1-34Code / dataset availability confirmedCrossref · checked 5 Sept 2026
ABSTRACT Sample preparation is an important first step to obtain high quality mass spectrometry imaging (MSI) data. Preparing plant tissues is especially challenging for MSI of thin tissues along the lateral dimensions. The unique challenges involved with plant tissues, such as fragile cell walls, hydrophobic barriers, and specific tissue structures, often lead to inefficiency and difficulties in sample preparation. Imprinting plant tissues onto porous polytetrafluoroethylene (pPTFE) sheet has been widely used to extract internal metabolites in leaves and petals while keeping spatial resolution for MSI. However, pressure applications were typically made manually using a vise or pliers leading to low reproducibility and resolution in MS images. In this study, we introduce a home‐built pneumatic press (PNP) that has been designed to precisely control the pressure application parameters during imprinting. To evaluate the performance of the new device, Lemna minor fronds, Arabidopsis thaliana , and Bacopa monnieri leaves were imprinted onto the pPTFE with PNP, vise, or pliers, and matrix‐assisted laser desorption/ionization (MALDI) MSI was obtained on the imprints. The PNP showed dramatic improvements in reproducibility and image quality compared to manual pressure application tools.
Why it matches plant phenotyping methods植物組織の空間的な代謝物情報を再現性よく取得するための空気圧式インプリンティング装置を開発し、手動法と性能比較している。植物表現型取得に関わる試料調製・イメージング手法が中心である。
abstractIn this study, we introduce a home‐built pneumatic press (PNP) that has been designed to precisely control the pressure application parameters during imprinting.
Reproduction assets foundThe paper's MALDI-MSI data (imzML files of imprinted Lemna minor, Arabidopsis, and Bacopa tissues) are openly deposited in a paper-specific METASPACE project, as stated in the Data Availability Statement. No author analysis code or trained models are disclosed.Dataset · publicData Availability Statement
The data that support the findings of this study are openly available in METASPACE (https://metaspace2020.eu/project/pnp_ptfe_imprinting_plant).Open asset ↗METASPACE · pnp_ptfe_imprinting_planthtml-lines:230-307Code / dataset availability confirmedCrossref · checked 5 Sept 2026
Callus induction is a complex procedure in plant organ, cell, and tissue culture that underpins processes such as metabolite production, regeneration, and genetic transformation. It is important to monitor callus formation alongside subjective evaluations, which require labor-intensive care. In this research, the first curated lentil (Lens culinaris) callus dataset for instance segmentation was experimentally generated using three genotypes as one data set: Firat-87, Cagil, and Tigris. Leaf explants were cultured on MS medium fortified with different concentrations of gross regulators of BA and NAA to induce callus formation. Three biologically relevant stages, the leaf stage, the green callus, and the necrosis callus, were produced. During this process, 122 high-resolution images were obtained, resulting in 1185 total annotations across them. The dataset was evaluated across four successive generations (v5/7/8/11) of YOLO deep learning models under identical conditions using mAP, Dice coefficient, Precision, Recall, and IoU, together with efficiency metrics including parameter counts, FLOPs, and inference speed. The results show that anchor-based variants (YOLOv5/7) relied on predefined priors and showed limited boundary precision, whereas anchor-free designs (YOLOv8/11) used decoupled heads and direct center/boundary regression that provided clear advantages for callus structures. YOLOv8 reached the highest instance segmentation precision with mAP50@0.855, while it matched the accuracy with greater efficiency and achieved real-time inference with 166 FPS.
Why it matches plant phenotyping methods植物組織培養におけるカルスの形成段階・壊死状態を画像からインスタンスセグメンテーションする手法、データセット、モデル比較を中心に扱っており、植物状態の取得・定量化が本研究の主要な技術貢献である。
titleReal-Time Callus Instance Segmentation in Plant Tissue Culture Using Successive Generations of YOLO Architectures
Reproduction assets foundThe paper's lentil callus image dataset with annotations (122 images, 1185 annotations) is publicly available on Roboflow Universe per the Data Availability Statement. The YOLOv5 GitHub link and Ultralytics docs are generic third-party libraries, not authors' analysis code, and the FAO link is a cited reference, so allDataset · publicThe dataset used in this study, including annotated images for callus detection, is publicly available and can be accessed at Roboflow Universe: https://universe.roboflow.com/yunus-7v2b5/callus-hug7d , accessed on 13 September 2025. This repository contains all images and annotations generated and analyzed during the current study.Open asset ↗Roboflow Universe · callus-hug7dlines:314-345Code / dataset availability confirmedEurope PMC · checked 5 Sept 2026
Plants move chloroplasts in response to light, changing the optical properties of leaves. Low irradiance induces chloroplast accumulation, while high irradiance triggers chloroplast avoidance. Chloroplast movements may be monitored through changes in leaf transmittance and reflectance, typically in red light. We present a step-by-step procedure for the detection of chloroplast positioning using reflectance hyperspectral imaging in white light. We show how to employ machine learning methods to classify leaves according to the chloroplast positioning. The convolutional network is a method of choice for the analysis of the reflectance spectra, as it allows low levels of misclassification. As a complementary approach, we propose a vegetation index, called the Chloroplast Movement Index (CMI), which is sensitive to chloroplast positioning. Our method offers a high-throughput, contactless way of chloroplast movement detection. Key features • Protocol for detached leaves handled in laboratory conditions. • Based on differential (dark-adapted versus irradiated) hyperspectral images of plant leaves. • Data analysis includes machine learning methods and the calculation of a vegetation index. • Requires irradiation equipment apart from the hyperspectral camera set.
Why it matches plant phenotyping methods葉の反射ハイパースペクトル画像から葉緑体位置を検出・分類する手法と指標を開発し、高スループット測定として提示しており、植物表現型取得が中心である。
abstractWe present a step-by-step procedure for the detection of chloroplast positioning using reflectance hyperspectral imaging in white light.
Reproduction assets foundThe protocol explicitly deposits its authors' analysis code (HyperspectralImageProcessing.m, including the pretrained CNN classifier for chloroplast positioning) on GitHub and makes the original hyperspectral images of Arabidopsis and Nicotiana leaves used in the paper's figures available on figshare. Both are paper-‐Code · publicAll code has been deposited to GitHub: https://github.com/plantPhotobiologyLab/machine-learning-for-chloroplast-movement-detection (access date, 08/18/2025)Open asset ↗plantPhotobiologyLab/machine-learning-for-chloroplast-movement-detectionhtml-lines:104-130Dataset · publicOriginal files with hyperspectral images of Nicotiana benthamiana and Arabidopsis thaliana (WT and phot2) leaves, including recordings shown in Figure 3 and Figure 4 of this protocol, can be downloaded from https://figshare.com/articles/dataset/Hyperspectral_images_of_Arabidopsis_thaliana_and_Nicotiana_benthamiana_leaves/30402409?file=58898569Open asset ↗html-lines:104-130Code / dataset availability confirmedEurope PMC · bioRxiv · Crossref · checked 14 Sept 2026
Volume electron microscopy (vEM) provides nanometer-scale, three-dimensional imaging of cells, but applying it to plant systems remains challenging. Cell walls, large vacuoles, and tissue thickness complicate sample preparation and cryogenic imaging. Here we report a cryogenic vEM (cryo-vEM) workflow for unstained plant protoplasts that achieves volumetric imaging of whole vitrified sorghum stem protoplasts without chemical fixation, dehydration, resin embedding, or heavy-metal staining. The method integrates optimized protoplast isolation, plunge-freezing vitrification for native-state preservation, automated cryogenic focus ion beam scanning electron microscopy (cryo-FIB-SEM) slice-and-view acquisition, contrast enhancement and stack alignment, and AI-assisted human-in-the-loop 3D segmentation. Using sorghum stem protoplasts as a demonstration, the workflow captured large-volume frozen-hydrated protoplast ultrastructure, allowing visualization of major organelles, including the nucleus, mitochondria, vacuoles, ER/Golgi-like membranes, lipid bodies, and subcellular features consistent with nuclear-envelope pores. We further quantified organelle volumes and surface areas from the segmented 3D data, highlighting the potential for quantitative cellular ultrastructure analysis. This cryo-vEM workflow provides a platform for near-native structural studies of isolated plant protoplasts.
Why it matches plant phenotyping methods植物プロトプラストの三次元画像取得・セグメンテーション・オルガネラ形態量化を中核とする手法開発であり、植物の細胞形態形質を抽出するため。
abstractHere we report a cryogenic vEM (cryo-vEM) workflow for unstained plant protoplasts that achieves volumetric imaging of whole vitrified sorghum stem protoplasts
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · public369 The codes are freely available at https://github.com/xzhang0123/vEMOpen asset ↗https://github.com/xzhang0123/vEM · xzhang0123/vEMpdf-page:10 lines:1-24Code / dataset availability confirmedCrossref · OpenAlex · checked 6 Sept 2026
SoybeanLaboratory / benchtopRootMorphology / geometry measurement2D/3D reconstructionSegmentationVisualization / data managementRoot system architecture
Root system analysis remains methodologically challenging in plant research: traditional soil cultivation obstructs comprehensive root observation, whereas hydroponic visualization lacks ecological relevance due to soil environment exclusion—a critical limitation for crops like soybean. This manuscript developed a cost-effective hybrid imaging system integrating transparent acrylic plates, semi-permeable membranes, and natural soil substrates with high-resolution imaging and controlled illumination, enabling non-destructive root monitoring in quasi-natural soil conditions. Complementing this hardware innovation, this manuscript proposed an unsupervised semantic segmentation algorithm that synergizes path planning with an enhanced DBSCAN framework, achieving the precise extraction of primary and lateral root architectures. Experimental validation demonstrated superior performance in soybean root analysis, with segmentation metrics reaching 0.8444 accuracy, 0.9203 recall, 0.8743 F1-score, and 0.7921 mIoU—significantly outperforming existing unsupervised methods (p 0.94) with WinRHIZO in quantifying root length, projected area, dimensional parameters, and lateral root counts confirmed system reliability. This soil-compatible phenotyping platform establishes new opportunities for root research, with future developments targeting multi-crop adaptability and complex soil condition applications through modular hardware redesign and 3D reconstruction algorithm integration.
Why it matches plant phenotyping methods根系観察用ハードウェアと画像セグメンテーション手法を開発し、根形質抽出性能を検証した、中心的な植物フェノタイピング研究である。
abstractThis manuscript developed a cost-effective hybrid imaging system
Reproduction assets foundThe paper's Data Availability Statement explicitly deposits the study's soybean root image data (the time-series NRMS dataset and scanner validation dataset used for phenotyping) in a public GitHub repository under the authors' account, matching an allowed URL. No separate analysis code availability is stated, so the资产Dataset · publicData Availability Statement: The data presented in this study are openly available in [GitHub] at
[https://github.com/xusiyue/RootPO_DBSCAN/tree/master/project_rootSystem/data (accessed
on 31 October 2025)].Open asset ↗GitHub · xusiyue/RootPO_DBSCANpdf-page:18 lines:1-58Code / dataset availability confirmedCrossref · Europe PMC · checked 6 Sept 2026
Studying the mechanisms that promote deep rooting in crops is crucial for engineering plant varieties with enhanced drought resilience and increased carbon sequestration capacity. Soil compaction is a major constraint on rooting depth and, to overcome this, root system penetrability needs to be enhanced. However, because of the limitations of current methods, phenotyping root penetrability remains a bottleneck. Here, we developed RootXplorer, a computer vision-based 3D phenotyping platform for high-throughput quantification of root penetration-related traits/phenotypes across dicot and monocot species. RootXplorer integrates a novel Phytagel-based cylinder system, a 3D imaging unit, and an automated software pipeline to extract root penetration-related traits with high precision and at a large scale. We demonstrate that RootXplorer enables large-scale diversity screenings in conditions replicating soil compaction effects in multiple species, revealing species-specific strategies for overcoming mechanical impedance. These findings highlight the utility and promise of RootXplorer for accelerating research on root architectural plasticity under controlled compaction conditions, identifying genotypes with varying tolerance to mechanical impedance, and supporting data-driven breeding decisions for developing soil compaction-resilient crop varieties. This technology has important implications for future plant breeding strategies and supports ongoing climate change mitigation efforts.
Why it matches plant phenotyping methodsRoot penetrability関連形質を対象に、3D画像計測と自動ソフトウェアで抽出する高スループット表現型解析プラットフォームを開発しており、方法が研究の中心です。
abstractRootXplorer integrates a novel Phytagel-based cylinder system, a 3D imaging unit, and an automated software pipeline to extract root penetration-related traits with high precision and at a large scale.
Reproduction assets foundThe paper's Data Availability statement explicitly deposits the complete analysis pipeline and time-lapse video generation code in two public GitHub repositories under the authors' Salk Harnessing Plants Initiative organization. These directly support the paper's RootXplorer phenotyping analysis (image cropping, U-Net+Code · publicAll code for generating time-lapse videos is publicly available at https://github.com/Salk-Harnessing-Plants-Initiative/RootXplorer-cylinder-time-lapseOpen asset ↗Salk-Harnessing-Plants-Initiative/RootXplorer-cylinder-time-lapselines:167-180Code / dataset availability confirmedOpenAlex · checked 15 Sept 2026
Published19 Nov 2025ISPRS Journal of Photogrammetry and Remote SensingCited by 3 · OpenAlex ↗
Accurate fruit shape reconstruction under real-world field conditions is essential for high-throughput phenotyping, sensor-based yield estimation, and orchard management. Existing approaches based on 2D imaging or explicit 3D reconstruction often suffer from occlusions, sparse views, and complex scene dynamics as a result of the plant geometries. This paper presents a novel UAV-based monocular 3D panoptic mapping framework for robust and scalable fruit shape completion in orchards. The proposed method integrates (1) Grounded-SAM2 for multi-object tracking and segmentation (MOTS), (2) photogrammetric structure-from-motion for 3D scene reconstruction, and (3) DeepSDF, an implicit neural representation, for completing occluded fruit geometries with a neural network. We furthermore propose a new MOTS evaluation protocol to assess tracking performance without requiring ground truth annotations. Experiments conducted in both controlled laboratory conditions and an operational apple orchard demonstrate the accuracy of our 3D fruit reconstruction at the centimeter level. The Chamfer distance error of the proposed shape completion method using the DeepSDF shape prior reduces this to the millimeter level, and outperforms the traditional method, while Grounded-SAM2 enables robust fruit tracking across challenging viewpoints. The approach is highly scalable and applicable to real-world agricultural scenarios, offering a promising solution to reconstruct complete fruits with visibility higher than 10% for precise 3D fruit phenotyping at a large scale under occluded conditions.
Why it matches plant phenotyping methods果実形状を対象とするUAV画像・3D再構成・形状補完法を開発し、実験で精度評価しており、植物表現型取得が研究の中心である。
abstractThis paper presents a novel UAV-based monocular 3D panoptic mapping framework for robust and scalable fruit shape completion in orchards.
Reproduction assets foundThe paper's authors publicly release their UAV orchard video data, lab 3D apple scans, and analysis code via a GitHub repository explicitly stated in the text. A Zenodo deposit (10.5281/zenodo.15635994) is also mentioned for the data, but its URL is not among the allowed URLs, so only the GitHub asset is reported.Code · publicing in orchard environments,(2) to propose a novel method to evaluate
MOTS without any annotations, and (3) to provide a highly accurate
3D apple dataset collected in a laboratory environment, along with
UAV-captured high-resolution videos in the field. The dataset and codes
for this research are publicly available at: https://github.com/Kaiwen-Robotics/Mono3DOrchard.2. Study area and materials
This study contains two data collection areas: field data collection
and laboratory data collection.
2.1. Field data collection
2.1.1. Study area
The field data collection was conducted within an apple orchard
located in Randwijk, Overbetuwe, the Netherlands (51.9376, 5.703057
in WGS84 UTM 31U), as shOpen asset ↗Kaiwen-Robotics/Mono3DOrchard.2pdf-raw-page:2 lines:75-128Code / dataset availability confirmedCrossref · Europe PMC · checked 13 Sept 2026
In this study, we present a pilot investigation using a single Purple Heart plant (Tradescantia pallida) to explore whether bioelectrical signals for dual-purpose classification tasks: environmental state detection and human emotion recognition. Using an AD8232 ECG sensor at 400 Hz sampling rate, we recorded 3 s bioelectrical signal segments with 1 s overlap, converting them to mel-spectrograms for ResNet18 CNN (Convolutional Neural Network) classification. For lamp on/off detection, we achieved 85.4% accuracy with balanced precision (0.85–0.86) and recall (0.84–0.86) metrics across 2767 spectrogram samples. For human emotion classification, our system achieved optimal performance at 73% accuracy with 1 s lag, distinguishing between happy and sad emotional states across 1619 samples. These results should be viewed as preliminary and exploratory, demonstrating feasibility rather than definitive evidence of plant-based emotion sensing. Replication across plants, days, and experimental sites will be essential to establish robustness. The current study is limited by a single-plant setup, modest sample size, and reliance on human face-tracking labels, which together preclude strong claims about generalizability.
Why it matches plant phenotyping methods植物の生体電気信号をセンサーで取得し、スペクトログラムとCNNで環境状態を分類する手法を開発・評価しており、植物の生理状態に基づく表現型取得が中心です。ただし、人間の感情分類は植物表現型ではありません。
abstractUsing an AD8232 ECG sensor at 400 Hz sampling rate, we recorded 3 s bioelectrical signal segments with 1 s overlap, converting them to mel-spectrograms for ResNet18 CNN (Convolutional Neural Network) classification.
Reproduction assets foundThe paper's Data Availability Statement provides explicit public URLs for both the phenotype/bioelectrical signal dataset (figshare project) and the authors' analysis code (GitHub), directly reproducing this paper's plant-phenotyping measurements and computational analysis.Dataset · publicThe data is available at https://figshare.com/projects/Plant_Bioelectrical_Signals_for_Environmental_and_Emotional_State_Classification/265783 (accessed on 25 October 2025).Open asset ↗figshare · Plant_Bioelectrical_Signals_for_Environmental_and_Emotional_State_Classification/265783lines:129-206Code · publicCode is available at https://github.com/pgloor/hiddenbiosignals (accessed on 25 October 2025).Open asset ↗github · pgloor/hiddenbiosignalslines:129-206Code / dataset availability confirmedCrossref · checked 15 Sept 2026
Abstract. Carbonyl sulfide (COS) has been proposed as a proxy for gross primary production (GPP), as it is taken up by plants through a pathway comparable to that of CO2. COS diffuses into the leaf, where it undergoes an essentially one-way reaction in the mesophyll cells, irreversibly catalyzed by the enzyme carbonic anhydrase (CA), and is likely not respired by the leaf. In order to use COS as a proxy for GPP, the mechanisms of COS uptake and its coupling to photosynthesis need to be well understood. Characterizing the isotopic discrimination of COS during plant uptake could provide valuable information on the physiological COS uptake process and may help to constrain the COS budget. This study presents joint measurements of isotope discrimination during plant uptake for COS (CO34S) and CO2 (13CO2 and C18O16O). A C3 plant, sunflower (Helianthus annuus), and a C4 plant, papyrus (Cyperus papyrus), were enclosed in a flow-through plant chamber and exposed to varying light levels. The incoming and outgoing gas compositions were measured online, and discrete air samples were taken for isotope analysis. Simultaneously measuring fluxes and isotope discrimination of both COS and CO2 yielded a unique dataset that includes information on the plant's behavior and allowed for the estimation of stomatal- and mesophyll conductances. The average COS uptake fluxes were 73.3 ± 1.5 pmol m−2 s−1 for sunflower and 107.3 ± 1.5 pmol m−2 s−1 for papyrus (PAR > 0) and displayed virtually no trend with increasing PAR from 200 to 600 µmol m−2 s−1. The mean observed 34Δ for COS was 3.4 ± 1.0 ‰ for sunflower and 2.6 ± 1.0 ‰ for papyrus. 34Δ was stable across all light intensities, which could be explained by a sufficient stomatal opening and low variability in the ratio of mesophyll vs. ambient COS mole fraction, CmS/CaS. For both C3 and C4 plants, for CO2, a negative relationship was observed between the uptake flux and the isotopic discriminations 13Δ and 18Δ. The CO2 uptake and 13CO2 and C16O18O discriminations of sunflower have expected values for a C3 plant, while the low CO2 flux and high 13Δ and 18Δ values observed for papyrus were not in the typical C4 range, which was perhaps due to the relatively low light conditions during our experiments.
Why it matches plant phenotyping methods植物のCOS・CO2取り込み、同位体識別、気孔・葉肉コンダクタンスをフロースルー植物チャンバーで定量する生理的表現型測定が研究の中心であり、再利用可能な測定データセットと推定手法を提示している。
abstractThis study presents joint measurements of isotope discrimination during plant uptake for COS (CO34S) and CO2 (13CO2 and C18O16O).
Reproduction assets foundThe paper's isotope discrimination and gas-exchange dataset from the flow-through chamber experiments is publicly deposited on Zenodo by the authors.Dataset · publicynthetically available radiation at the top of the chamber, 34 Δ is the discrimination against CO 34 S and LRU is the leaf relative uptake ratio.
* n =1 , error states is the single measurement precision instead of the repeatability precision.
Download Print Version | Download XLSX
Data availability
The dataset is available at: https://doi.org/10.5281/zenodo.14677494 (Baartman et al., 2025).
Author contributions
Conceptualization: SLB, MCK, MEP, LW. Data curation: SLB. Formal analysis: SLB, NUL. Funding acquisition: MCK. Investigation: SLB, SMD, MW, LMJK, LM, AC, SH. Methodology: SLB, SMD, MW, LMJK, MEP. Resources: SMD, MW, LM, SH. Supervision: MEP, TR, MCK. Visualization: SLB, NUL. WritingOpen asset ↗Zenodo · 10.5281/zenodo.14677494lines:652-942Code / dataset availability confirmedOpenAlex · Europe PMC · checked 14 Sept 2026
Accurate 3D phenotyping of agricultural produce remains challenging due to the trade-off between reconstruction quality and acquisition throughput in existing sensing technologies. While RGB-D cameras enable high-throughput scanning in operational settings like harvesting conveyors, they produce incomplete, low-quality 3D models. Conversely, close-range Structure-from-Motion (SfM) produces high-quality reconstructions but is not suitable for high-throughput field application. This study bridges this gap through 3DPotatoTwin , a paired dataset containing 339 tuber samples across three cultivars collected in Hokkaido, Japan. Our dataset uniquely combines: (1) conveyor-acquired RGB-D point clouds, (2) ground measurement, (3) SfM reconstructions under indoor controlled environment, and (4) aligned model pairs with transformation matrices. The multi-sensory alignment employs an semi-supervised pin-guided pipeline incorporating single-pin extraction and referencing, cross-strip matching, and binary-color-enhanced ICP, achieving 0.59 ± 0.11 mm registration accuracy. Beyond serving as a benchmark for 3D phenotyping algorithms, the dataset enables training of 3D completion networks to reconstruct high-quality 3D models from partial RGB-D point clouds. Meanwhile, the proposed semi-automated annotation pipeline has the potential to accelerate 3D dataset generation for similar studies. The presented methodology demonstrates broader applicability for multi-sensor data fusion across crop phenotyping applications. The dataset and pipeline source code are publicly available at HuggingFace and GitHub, respectively.
Why it matches plant phenotyping methodsジャガイモ塊茎の3D表現型計測を対象に、RGB-D・SfM・地上計測を統合したデータセット、位置合わせパイプライン、ベンチマークを開発しており、表現型取得手法が中心である。
abstractAccurate 3D phenotyping of agricultural produce remains challenging due to the trade-off between reconstruction quality and acquisition throughput in existing sensing technologies.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicAll the batch processing scripts mentioned in this section were provided in the 3dscan folder at Github (https://github.com/UTokyo-FieldPhenomics-Lab/PotatoScan/).Open asset ↗UTokyo-FieldPhenomics-Lab/PotatoScanhtml-lines:119-131Code / dataset availability confirmedOpenAlex · Crossref · Europe PMC · checked 6 Sept 2026
Introduction: spp.) is a perennial legume traditionally cultivated as a forage crop and is now emerging as a promising candidate for development as a perennial grain legume. Despite its potential, no research has addressed the breeding of sainfoin varieties with superior grain processing properties. Methods: We conducted a multifactorial experiment to evaluate the depodding and dehulling efficiency of five commercially available sainfoin varieties. Seeds were processed using two different methods (belt thresher and impact dehuller) across five sample sizes. A pre-trained Faster R-CNN (Region-based Convolutional Neural Network) object detection model was fine-tuned to identify intact pods, whole seeds, and split seeds from images of the processed mixtures. These predictions were used to calculate processing efficiency (PE) for each variety. A comprehensive power analysis was performed to determine the minimum sample size of sainfoin pods required to detect differences in PE with high statistical power. Results: We observed strong varietal differences in PE, as well as clear effects of the processing method. Belt threshing produced mixtures with more intact pods, while the impact dehuller generated a higher proportion of split seeds. Increasing sample size led to more intact pods across all varieties and methods, and notably decreased seed proportion in belt-threshed samples. Statistical modeling combined with object detection outputs revealed that a minimum of 2 g of pods is required to reliably detect an absolute proportional difference of 0.25 in PE between two breeding lines with 80% power. Discussion: Our findings demonstrate that sainfoin varieties differ significantly in processing efficiency and that processing outcomes depend strongly on both method and sample size. Integrating deep learning-based phenotyping with robust statistical design enables efficient evaluation of processing traits and provides actionable guidelines for breeding programs. While deep learning models offer powerful, cost-effective tools for plant phenotyping, their outputs must be paired with rigorous statistical design to yield reliable and actionable insights for crop improvement.
Why it matches plant phenotyping methods画像からポッド・種子を検出し、処理効率という植物由来形質を算出する深層学習ベースの表現型解析が研究の中心であるため。
titleDeep learning driven, image-based phenotyping of seed processing efficiency in sainfoin
Reproduction assets foundThe paper's data availability statement explicitly deposits the seed image dataset and Faster R-CNN model weights in two public Zenodo repositories and all Python/R analysis code in a public GitHub repository, all with direct URLs.Dataset · publicThe image dataset and FasterRCNN model weights presented in the study are deposited in publicly available Zenodo repositories under accession numbers https://doi.org/10.5281/zenodo.8346923Open asset ↗Zenodo · 10.5281/zenodo.8346923lines:501-517Code · publicAll Python and R code used in this study are deposited in a public GitHub repository at https://github.com/BoMeyering/sainfoin_seed_RCNNOpen asset ↗GitHub · BoMeyering/sainfoin_seed_RCNNlines:501-517Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
Laboratory / benchtopRGB / grayscaleFruitClassificationGrowth / development / phenology
Okra is a highly nutritious farming product that combats malnutrition issues while supporting sustainable agricultural methods. In order to keep its quality and versatility in preparation applications, it is important to classify its maturity stages into under-mature, mature, and over-mature categories. Classification is vital to identify the best time to harvest, satisfy market demands, minimize post-harvest losses, and optimize cooking uses. This data in brief uses a non-destructive approach to okra maturity classification based on a dataset of images taken under controlled illumination using a standard RGB camera. The dataset contains okra samples that were sourced from various farms and vegetable markets, ensuring that it encapsulates the natural variability found in real-world farm and market environments. The availability of such a large dataset enables the creation of precise classification models that can assist farmers in optimizing the time of harvest, fulfilling consumers' requirements, and improving market results. The research has great relevance to promoting agricultural quality evaluation and boosting market readiness using non-invasive techniques.
Why it matches plant phenotyping methodsRGB画像データセットによるオクラ果実の成熟段階分類が研究の中心であり、植物器官の状態を画像から推定する再利用可能なフェノタイピング資源に該当する。
titleRGB image dataset for okra maturity classification to enhance agricultural quality and market readiness.
Reproduction assets foundThe paper is a Data in Brief article whose core contribution is a public RGB okra image dataset (364 images across three maturity classes) deposited on Mendeley Data, directly serving as the paper's phenotyping image asset. No separate analysis code repository is described.Dataset · publicVellore Institute of Technology - Chennai Campus.
City/Country: Chennai, India.
Latitude and longitude for collected samples/data: (12.8406° N, 80.1534° E), Vellore Institute of Technology - Chennai.
Data accessibility
Repository name: Okra Image Dataset
Data identification number: DOI: 10.17632/jmhz4826f2.1
Direct URL to data: https://data.mendeley.com/datasets/jmhz4826f2/1
Related research article
[ 1 ]
1
Value of the Data
•
Agricultural quality assessment is advancing through non-invasive methods that include the use of RGB image analysis for effective determination of okra maturity stages.
•
Utilization of ML and DL methods in recognizing visual characteristics, i.e., color, texture, andOpen asset ↗10.17632/jmhz4826f2.1lines:1-56Code / dataset availability confirmedEurope PMC · bioRxiv · checked 14 Sept 2026
Background The plant vacuole arises by orchestrated interplay of membrane trafficking, cytoskeletal rearrangements and a variety of signalling pathways. In the root, the characteristic large central vacuole develops by endomembrane reorganization occurring mainly in the transition zone. The vacuole’s bounding membrane - the tonoplast - can be visualized in vivo using fluorescent protein markers, allowing for quantitative analysis of confocal microscopy images. Tonoplast organization can thus serve as a sensitive indicator of changes to any of the processes involved in vacuole biogenesis. The Vacuolar Morphology Index (VMI) is widely accepted as a quantitative measure of vacuole structure. However, this metric has two drawbacks - it only reflects the size of the largest vacuolar compartment (missing therefore possible differences in the organization of smaller compartments), and its determination is labor intensive, limiting its use on large datasets. Results We developed an alternative metric for describing vacuole organization, named the Tonoplast Topology Index (TTI), which overcomes the above-mentioned shortcomings of the VMI. We compared the performance of our protocol with VMI on a simulated dataset and on real data. To validate the methods’ performance, we used it to confirm the previously reported differences in vacuole shape and size between Arabidopsis thaliana roots grown on the surface of an agar medium compared to those embedded inside the agar. Both VMI and TTI could efficiently detect the relatively subtle changes in vacuole organization depending on the position of the root in the agar, and provided correlated results. However, only TTI produced data with close to normal value distribution, simplifying subsequent statistical evaluation. Conclusions We present the protocol for TTI determination as a two-stage semi-automated procedure involving microscopic image analysis employing an ImageJ macro and subsequent processing of numeric data in the Jupyter Notebook environment, together with benchmarking image data. Since this implementation is freeware-based, platform-independent and (relatively) user-friendly, we hope it will find its use as a high throughput, added value alternative to the VMI metric.
Why it matches plant phenotyping methods植物の液胞構造を定量化する新規指標と半自動画像解析プロトコルを開発し、既存指標との比較・実データおよびシミュレーションによる検証、ベンチマークデータを提示しており、表現型取得・抽出法が中心である。
abstractWe developed an alternative metric for describing vacuole organization, named the Tonoplast Topology Index (TTI), which overcomes the above-mentioned shortcomings of the VMI.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicthe software tool generated here are also available at https://github.com/GeorgeCaldarescu/TTI-Open asset ↗GeorgeCaldarescu/TTI-pdf-page:9 lines:1-52Code / dataset availability confirmedEurope PMC · OpenAlex · checked 13 Sept 2026
Abstract To watch the growth of 1200 P. sylvestris cv. Negorelskaya trees from seeds to young or even old stage is a big grant project. We want to make a «seed–culture» passport. Each individual seed (N = 1200) was weighed, and image acquisition via a flatbed scanner in the VIS wavelength region and seeded into an individual 120 cm 3 cell of a 40-cell container. On day 30, container-grown germination was evaluated according to the following dichotomous criterion: 1 – germinated (n 1 = 942), 0 – did not germinate (n 0 = 258), and 0-group and 1-group datasets were formed. The RGB space color of the individual seed epidermis between the 0- and the 1-group were compared via the Kolmogorov‒Smirnov criterion D. The lower individual weight of the seed in the 0-group compared with the 1-group was not accidental (p = 0.0045). Additionally, in the 0 group, the median values of R, G, and B brightness of pixels from individual seeds are not accidental (p = 0.0000381) compared with those of the 1 group. Therefore, in this experiment, seeds that reflected most of the light from the epidermis showed a lower germination when placed in the container.
Why it matches plant phenotyping methods個体種子を対象にスキャナ画像からRGB形質を抽出し、発芽との関連を評価する画像ベースの表現型取得が研究の中心である。
abstractimage acquisition via a flatbed scanner in the VIS wavelength region
Reproduction assets foundThe paper's data availability statement openly deposits all three paper-specific phenotyping assets in Mendeley Data: Dataset 1 (individual seed morphometric/weight data, N=1200), Dataset 2 (original VIS flatbed-scanner seed images, N=1200), and Dataset 3 (individual container germination data, N=1200). These directly供Dataset · publicThe original morphometric data—Dataset 1—of Pinus sylvestris L. сv. The individual Negorelskaya seeds (N = 1200) presented in the study are openly available in Mendeley Data at DOI : https://doi.org/10.17632/8g258nbgmf.1.Open asset ↗Mendeley Data · 10.17632/8g258nbgmf.1lines:152-174Dataset · publicThe original VIS image data of Pinus sylvestris L. сv. The individual Negorelskaya seeds (N = 1200) presented in the study are openly available in Mendeley Data at DOI : https://doi.org/10.17632/dt78jhyw2j.2.Open asset ↗Mendeley Data · 10.17632/dt78jhyw2j.2lines:152-174Dataset · publicThe original germination data—Dataset 3—of Pinus sylvestris L. cv. The individual Negorelskaya seeds (N = 1200) presented in the study are openly available in Mendeley Data at DOI : https://doi.org/10.17632/hrs3fgc8tt.1.Open asset ↗Mendeley Data · 10.17632/hrs3fgc8tt.1lines:152-174Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
AppleLaboratory / benchtopMultispectral / hyperspectralFruitClassificationGrowth / development / phenology
The study created a detailed database for apple quality inspection using a cost-effective, self-designed multi-spectral imaging system. The system was optimized to allow spectral information to be obtained in 8 discrete wavebands, which enabled non-destructive determination of such key fruit components as ripeness, sugar type and cultivar. Stringent environmental conditions were maintained during image acquisition for optimal measurement consistency and experimental repeatability. The detailed dataset encompasses 32,463 multi-spectral images across three distinct classification categories. For sweetness evaluation, 1620 images spanning Brix values from 10 % to 15 % were collected from five apple varieties. Ripeness evaluation includes 29,160 images documenting the complete maturation cycle over 18 days, while variety classification contains 1683 images from three distinct cultivars. Each image was captured under controlled lighting conditions using eight specific wavelengths, ensuring spectral consistency crucial for machine learning applications. These multi-spectral images were concatenated for grading by sweetness, ripeness, and variety, creating a processed dataset of concatenated images optimized for AppleNet processing. The concatenation process combines the eight wavelength channels into unified image representations suitable for deep learning applications. Sample collection included the picking of different apple cultivars at different physiological development phases of fruit from local orchards. Single specimens were imaged sequentially using a multi-spectral technique. Information on sugar content concentration ( % Brix), maturation phase classification and varietal identification was recorded according to standard laboratory procedure. The resulting annotated database includes such quantitative reference points, which can be used to train supervised learning classifiers in computational classification systems. The reuse value of the dataset covers a wide range of applications such as machine learning-based fruit quality evaluation, agricultural automation and food industry examination. This dataset of ours can be used by researchers to develop and test algorithms to classify apples and estimate their ripeness and the presence of diseases. Furthermore, the proposed multi-spectral imaging can be generalized to cover other fruits and agricultural products, extending the application of the method in smart agriculture. This dataset serves as a valuable resource for researchers in computer vision, machine learning, and agricultural technology, fostering advancements in non-destructive fruit quality evaluation methodologies.
Why it matches plant phenotyping methodsリンゴの甘度・成熟度・品種を推定するマルチスペクトル撮像システムと、注釈付き大規模画像データセットを中心に構築しており、植物器官の品質・状態を定量化する再利用可能なフェノタイピング手法に該当する。
abstractThe study created a detailed database for apple quality inspection using a cost-effective, self-designed multi-spectral imaging system.
Reproduction assets foundThe article is a Data in Brief describing a public multi-spectral apple image dataset (sweetness/Brix, ripeness over 18 days, variety) deposited on Mendeley Data with DOI 10.17632/y5h6v8w6ms.2 and a direct URL, explicitly stated as publicly accessible. This is the paper's own phenotyping image dataset. The MATLAB code,Dataset · publicme environment using a custom-built multi-spectral imaging chamber . The imaging conditions were carefully maintained to ensure consistency. The dataset is securely stored for research and study purposes.
Data accessibility
Repository name: Mendeley Data
Data identification number: DOI: 10.17632/y5h6v8w6ms.2
Direct URL to data: https://data.mendeley.com/datasets/y5h6v8w6ms/2
Instructions for accessing these data:
Dataset Title: Dataset of Apples for Grading by Sweetness, Ripeness, and Variety
Public Access: The dataset titled ``Dataset of Apples for Grading by Sweetness, Ripeness, and Variety'' is publicly available on Mendeley Data and can be accessed via the following DOI:
https://doi.org/Open asset ↗Mendeley Data · 10.17632/y5h6v8w6ms.2lines:40-82Code / dataset availability confirmedEurope PMC · checked 6 Sept 2026
Laboratory / benchtopX-ray / CTRootMorphology / geometry measurementRoot system architecture
Soil compaction and escalating global drought increase soil strength and stiffness. It remains unclear which plant root biomechanical mechanisms/traits enable growth in these harsh conditions. Here, we combine synchrotron X-ray computed tomography with spatially resolved X-ray diffraction to characterize the biomechanics of a replica root-soil system. We map the strain field around the root tip analog, finding strong agreement with finite element simulations, thereby demonstrating a promising new in vivo measurement protocol.
Why it matches plant phenotyping methods根の生育に関わる土壌内の力学的状態・ひずみを、X線CTと回折で可視化・定量する新しいin vivo測定プロトコルを開発・検証しており、植物表現型取得法が中心です。
abstractWe map the strain field around the root tip analog, finding strong agreement with finite element simulations, thereby demonstrating a promising new in vivo measurement protocol.
Reproduction assets foundThe paper's Data availability and Code availability statements both deposit the study's XCT/XRD imaging and diffraction data and the processing scripts in the University of Southampton Pure repository (DOI 10.5258/SOTON/D3309), which is an allowed URL. These are paper-specific, publicly declared assets directly reproduCode · publicAll scripts used to process the data can be found in the Pure repository: https://doi.org/10.5258/SOTON/D3309 .Open asset ↗Pure · 10.5258/SOTON/D3309lines:209-251Code / dataset availability confirmedCrossref · Europe PMC · checked 15 Sept 2026
The integration of nanotechnology in agriculture allows for more precise nutrient delivery through nanoparticles (NPs), particularly via foliar application. To mature this technology for enhancing fertilizer efficiency, it is essential to shed new light on the transport and dissolution of NPs in plants. Available analytical methods struggle to address this challenge in a direct manner. We introduce correlative X-ray imaging as a novel analytical tool capable of tracking NP pathways, dissolution and hence nutrient release in plants. By utilizing three complementary X-ray techniques, we offer a unique insight into the plant processes associated with foliar fertilization. We demonstrate that small-angle X-ray scattering enables the characterization of NP size and concentration, while X-ray fluorescence imaging, maps the distribution of elements within the sample. Finally, micro-computed tomography integrates these findings into a complete three-dimensional digital representation of the plant’s microstructure, revealing regions of apparent densification associated with NP accumulation. Using freeze-dried barley plants infiltrated with nano-hydroxyapatite (nHAP), we observed rapid dissolution of NPs, and we are able to associate time and space attributes to the translocation process of nutrients up to three days following foliar application of NPs. With the first pilot study of applying correlative X-ray imaging to live plants, we sought to indicate the potential of this new analytical approach for future nano-enabled agricultural research.
Why it matches plant phenotyping methods植物内のナノ粒子経路・溶解・栄養輸送を可視化する相関X線イメージング手法の導入と実証が中心であり、植物の状態・生理過程を測定する方法論的研究である。
abstractWe introduce correlative X-ray imaging as a novel analytical tool capable of tracking NP pathways, dissolution and hence nutrient release in plants.
Reproduction assets foundThe article's data availability statement points to a public figshare repository hosting the study's datasets (X-ray imaging/phenotyping measurements). No author analysis code with explicit public deposit language was identified; Dragonfly is a commercial visualization tool, not a paper-specific asset.Dataset · publicng Wan , Hainan University, China
Zhansheng Li , Chinese Academy of Agricultural Sciences, China
Firozeh Solimani , Politecnico di Bari, Italy
Data availability statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://figshare.com/s/33ee8388a36600fe98d5 .
Author contributionsOpen asset ↗figsharelines:191-206Code / dataset availability confirmedbioRxiv · checked 15 Sept 2026
The global carbon cycle depends heavily on the carbon sequestration rates of aquatic ecosystems. Sinking of phytoplankton is a rapid mediator of carbon sequestration, because phytoplankton are globally abundant photoautotrophs that grow rapidly. Pico- and nano-phytoplankton sinking velocities vary depending on their growth state, viability, clumping, and distribution in the water column. We introduced high throughput fluorescence microscopy of well-plates, to measure sinking velocities of three diatom strains, and three cyanobacteria strains, with cell radii spanning an order of magnitude, all grown under three different light levels. Cultures were measured for sinking velocities repeatedly across their growth trajectories. Tracking multiple fluorescence wavebands allowed us to simultaneously determine sinking velocities for living vs. dead cells. Sinking velocities varied strongly across growth light levels, and across growth stages. These monoclonal cultures furthermore show distinct sub-populations of slow- and fast-sinking cells. Our results departed widely from simple Stokes Law estimates of sinking based upon radii and mass density of cells. Complex, heterogeneous phytoplankton communities likely show more complicated sinking patterns than are currently expressed in biogeochemical ocean models. Our well-plate microscopy approach using parallel imaging of many samples generates high-throughput measures of cell sinking at population- or community-scales, to in turn improve modelling of carbon export to deeper layers.
Why it matches plant phenotyping methods植物プランクトンの沈降速度を高スループット蛍光顕微鏡で測定する手法を導入し、生活状態や集団スケールの生理・機能形質を定量化しているため、測定法が研究の中心です。
abstractWe introduced high throughput fluorescence microscopy of well-plates, to measure sinking velocities of three diatom strains, and three cyanobacteria strains
Reproduction assets foundThe paper's sinking-velocity analysis code is explicitly stated to be openly available on the authors' GitHub repository. The raw phenotype data is promised for Dryad only upon acceptance, so it is not yet publicly actionable.Code · publicfunctional groups of cyanobacteria, diatoms strains with 156
diameter less than 10µm and diatoms strains with diameter larger than 10µm based on 157
growth light, viability state (living vs. dead and dying) and slow vs. fast sinking 158
velocity clustering groups. 159
The code used to analyse the data is public available at 160
https://github.com/maxberthold/PhytoplanktonSinkVelocities. 161
Sinking according to Stokes’ law 162
Sinking velocities of spherical objects falling under the case of Reynolds numbers 163
smaller than 1 can be described by Stokes’ law. Several studies have used Stokes law or 164
a modified version of Stokes’ law to estimate sinking velocities of plankton and marine 16Open asset ↗maxberthold/PhytoplanktonSinkVelocitiespdf-raw-page:8 lines:1-44Code / dataset availability confirmedOpenAlex · Europe PMC · checked 15 Sept 2026
Various high-throughput screening methods have been developed to explore plant phenotypes, primarily at the organ and whole plant levels. There is a need to develop phenomics methods at the cellular level to narrow down the genotype to phenotype gap. This study used double-resonator piezoelectric cytometry biosensors to capture the dynamic changes in mechanical phenotypes of living cells of two rice species, drought-resistant Lvhan No. 1 and drought-sensitive 6527, under PEG6000 drought stress. In rice cells of Lvhan No. 1 and 6527, mechanomics parameters, including cell-generated surface stress (ΔS) and viscoelastic parameters (G', G″, G″/G'), were measured and compared under 5-25% PEG6000. Lvhan No. 1 showed larger viscoelastic but smaller surface stress changes with the same concentration of PEG6000. Moreover, Lvhan No. 1 cells showed better wall-plasma membrane-cytoskeleton continuum structure maintaining ability under drought stress, as proven by transient tension stress (ΔS > 0) and linear G'~ΔS, G″~ΔS relations at higher 15-25% PEG6000, but not for 6527 cells. Additionally, two distinct defense and drought resistance mechanisms were identified through dynamic G″/G' responses: (i) transient hardening followed by softening recovery under weak drought, and (ii) transient softening followed by hardening recovery under strong drought. The abilities of Lvhan No. 1 cells to both recover from transient hardening to softening and to recover from transient softening to hardening are better than those of 6527 cells. Overall, the dynamic mechanomics phenotypic patterns (ΔS, G', G″, G″/G', G'~ΔS, G″~ΔS) verified that Lvhan No. 1 has better drought resistance than that of 6527, which is consistent with the field data.
Why it matches plant phenotyping methods植物細胞の機械的表現型を取得する高スループットなバイオセンサー手法を用い、乾燥ストレス応答を定量化しており、表現型取得法が研究の中心である。
abstractThere is a need to develop phenomics methods at the cellular level to narrow down the genotype to phenotype gap.
Reproduction assets foundThe paper's DRPC phenotyping measurements (frequency and motional resistance traces underlying the ΔS, G′, G″ analyses) are provided as downloadable supplementary figures at the MDPI supplementary URL. No standalone public dataset or author analysis code repository is stated; the Data Availability Statement only offersSupplement · publicansient softening under strong drought. The results presented in this work demonstrated the potential to develop a new cellular mechanical phenotype platform to screen for biotic and abiotic stress-resistant crop varieties, as shown in Figure 11 .
Supplementary Materials
The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/bios15060334/s1 , Figure S1: Changes in frequency and motional resistance of 9 MHz AT and BT cut chips during the adhesions of Lvhan No.1 rice cells followed by the treatments of different concentrations of PEG6000 stresses. (A, B, C, D, E): AT cut, (A1, B1, C1, D1, E1): BT cut, (A, A1): 5% PEG6000, (B, B1): 10%PEG6000, (C, C1) 15%Open asset ↗lines:136-159Code / dataset availability confirmedOpenAlex · Crossref · Europe PMC · checked 6 Sept 2026
Introduction Recent advancements in sensor technologies have enabled collection of many large, high-resolution plant images datasets that could be used to non-destructively explore the relationships between genetics, environment and management factors on phenotype or the physical traits exhibited by plants. The phenotype data captured in these datasets could then be integrated into models of plant development and crop yield to more accurately predict how plants may grow as a result of changing management practices and climate conditions, better ensuring future food security. However, automated methods capable of reliably and efficiently extracting meaningful measurements of individual plant components (e.g. leaves, flowers, pods) from imagery of whole plants are currently lacking. In this study, we explore interdisciplinary application of MapReader, a computer vision pipeline for annotating and classifying patches of larger images that was originally developed for semantic exploration of historical maps, to time-series images of whole oilseed rape (Brassica napus) plants. Methods Models were trained to classify five plant structures in patches derived from whole plant images (branches, leaves, pods, flower buds and flowers), as well as background patches. Three modelling methods are compared: (i) 6-label multi-class classification, (ii) a chain of binary classifiers approach, and (iii) an approach combining binary classification of plant and background patches, followed by 5-label multi-class classification of plant structures. Results A combined plant/background binarization and 5-label multi-class modelling approach using a ‘resnext50d_4s2x40d’ model architecture for both the binary classification and multi-class classification components was found to produce the most accurate patch classification for whole B. napus plant images (macro-averaged F1-score = 88.50, weighted average F1-score = 97.71). This combined binary and 5-label multi-class classification approach demonstrate similar performance to the top-performing MapReader ‘railspace’ classification model. Discussion This highlights the potential applicability of the MapReader model framework to images data from across scientific and humanities domains, and the flexibility it provides in creating pipelines with different modelling approaches. The pipeline for dynamic plant phenotyping from whole plant images developed in this study could potentially be applied to imagery from varied laboratory conditions, and to images datasets of other plants of both agricultural and conservation concern.
Why it matches plant phenotyping methods植物全体画像から葉・花・莢などの構造を自動抽出・分類する動的フェノタイピング手法を開発・評価しており、方法が研究の中心である。
abstractautomated methods capable of reliably and efficiently extracting meaningful measurements of individual plant components (e.g. leaves, flowers, pods) from imagery of whole plants are currently lacking.
Reproduction assets foundThe paper's phenotyping analysis is based on a public RGB image dataset of Brassica napus plants, explicitly deposited by the authors with a public URL. MapReader is a generic pre-existing library and the HuggingFace railspace models are cited prior work, not paper-specific assets.Dataset · publicThe datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://research.aber.ac.uk/en/datasets/collection-of-side-view-and-top-view-rgb-images-of-brassica-napus .Open asset ↗research.aber.ac.uklines:982-1027Code / dataset availability confirmedCrossref · checked 13 Sept 2026
Abstract The timely and precise identification of diseases in plants is essential for efficient disease control and safeguarding of crops. Manual identification of diseases requires expert knowledge in the field, and finding people with domain knowledge is challenging. To overcome the challenge, computer vision-based machine learning techniques have been proposed by the researchers in recent years. Most of these solutions with the standard convolutional neural network (CNN) approaches use uniform background laboratory setup leaf images to identify the diseases. However, only a few works considered real-field images in their work. Therefore, there is a need for a robust CNN architecture that can identify the diseases in plants in both laboratory and real-field conditioned images. In this paper, we have proposed an Inception-enabled vision transformer (ViT) architecture to identify the diseases in plants. The proposed Inception-enabled ViT architecture extracts local as well as global features, which improves feature learning. The use of multiple filters with different kernel sizes efficiently use computing resources to extract relevant features without the need for deeper networks. The robustness of the proposed architecture is established by hyper-parameter tuning and comparison with state-of-the-art. In the experiment, we consider five datasets with both laboratory-conditioned and real-field conditioned images. From the experimental results, we see that the proposed model outperforms state-of-the-art deep learning models with fewer parameters. The proposed model archives an accuracy rate of 99.17% for the apple leaf dataset, 99.32% for the rice dataset, 96.89% for the ibean dataset, 75.42% for the cassava leaf dataset, and 99.33% for the plantvillage dataset.
Why it matches plant phenotyping methods植物病害の画像から病害状態を推定するコンピュータビジョン手法を開発・比較しており、植物表現型（病害状態）の抽出が中心です。
abstractIn this paper, we have proposed an Inception-enabled vision transformer (ViT) architecture to identify the diseases in plants.
Reproduction assets foundThe paper evaluates an Inception-enabled ViT model on five publicly available plant disease image datasets. The Data Availability section explicitly lists Kaggle URLs for the apple, bean (ibean), rice/wheat-rust, PlantVillage, and cassava datasets. These are public, paper-specific image datasets directly used for the模型Dataset · publicThe datasets generated and/or analysed during the current study
are available in Kaggle repository at:
https://www.kaggle.com/datasets/piantic/plantpathology-apple-datasetOpen asset ↗Kaggle · piantic/plantpathology-apple-datasetpdf-page:22 lines:1-48Code / dataset availability confirmedEurope PMC · OpenAlex · checked 6 Sept 2026
The need for more sustainable agricultural systems is becoming increasingly apparent. The global demand for agricultural products-food, feed, fuel and fiber-will continue to increase as the global population continues to grow. This challenge is compounded by climate change. Not only does a changing climate make it difficult to maintain stable yields but current agricultural systems are a major source of greenhouse gas emissions and continue to drive the problem further. Therefore, future agricultural systems must not only increase production but also significantly decrease negative environmental impacts. One approach to addressing this is to begin breeding and cultivating new plant species that have fundamental sustainability advantages over our existing crops. The Lemnaceae, commonly known as duckweeds, are one family of plants that have potential to increase output and reduce the negative environmental impacts of agricultural production. Herein we describe the Automated Lab-scale PHenotyping Apparatus, ALPHA, for high-throughput phenotyping of Lemnaceae. ALPHA is being used for selective breeding of one species, Lemna gibba , toward the goal of creating a new crop for use in sustainable agricultural systems. ALPHA can be used on many small aquatic plant species to assess growth rates in different environmental conditions. A proof of principle use case is demonstrated where ALPHA is used to determine saltwater tolerance of six different clones of L. gibba .
Why it matches plant phenotyping methodsALPHAは水生植物の成長率をハイスループットに定量化するための装置・表現型解析プラットフォームとして開発・実証されており、手法が研究の中心である。
abstractHerein we describe the Automated Lab-scale PHenotyping Apparatus, ALPHA, for high-throughput phenotyping of Lemnaceae.
Reproduction assets foundThe authors state that all source code for the phenotyping system and analysis, 3D models, and the data generated for this study (including PlantCV output and barcode map CSVs) are publicly available in the ALPHA GitHub repository.Dataset · publicAll source code used in the phenotyping system, 3D models for printed parts and data generated for this study are available in the ALPHA Github repository .Open asset ↗lines:85-105Code / dataset availability confirmedCrossref · checked 6 Sept 2026
The segmentation of plant disease images enables researchers to quantify the proportion of disease spots on leaves, known as disease severity. Current deep learning methods predominantly focus on single diseases, simple lesions, or laboratory-controlled environments. In this study, we established and publicly released image datasets of field scenarios for three diseases: soybean bacterial blight (SBB), wheat stripe rust (WSR), and cedar apple rust (CAR). We developed Plant Disease Segmentation Networks (PDSNets) based on LinkNet with ResNet-18 as the encoder, including three versions: ×1.0, ×0.75, and ×0.5. The ×1.0 version incorporates a 4 × 4 embedding layer to enhance prediction speed, while versions ×0.75 and ×0.5 are lightweight variants with reduced channel numbers within the same architecture. Their parameter counts are 11.53 M, 6.50 M, and 2.90 M, respectively. PDSNetx0.5 achieved an overall F1 score of 91.96%, an Intersection over Union (IoU) of 85.85% for segmentation, and a coefficient of determination (R2) of 0.908 for severity estimation. On a local central processing unit (CPU), PDSNetx0.5 demonstrated a prediction speed of 34.18 images (640 × 640 pixels) per second, which is 2.66 times faster than LinkNet. Our work provides an efficient and automated approach for assessing plant disease severity in field scenarios.
Why it matches plant phenotyping methods植物病害画像から病斑割合と病害重症度を推定する画像セグメンテーション手法を開発し、野外データセット、精度、速度を評価しており、植物表現型取得法が中心である。
abstractThe segmentation of plant disease images enables researchers to quantify the proportion of disease spots on leaves, known as disease severity.
Reproduction assets foundThe paper's field-scenario plant disease image dataset (SBB, WSR, CAR with three-color pixel labels) is publicly released on Kaggle via DOI, as stated in the Data Availability Statement. No author analysis code or trained model checkpoints are explicitly deposited.Dataset · publicData Availability Statement: The original data presented in this study are openly available in Kaggle
at https://doi.org/10.34740/kaggle/ds/6620728, accessed on 9 March 2025.Open asset ↗Kaggle · 10.34740/kaggle/ds/6620728pdf-page:15 lines:1-58Code / dataset availability confirmedOpenAlex · Europe PMC · checked 6 Sept 2026
Machine learning models for crop image analysis and phenomics are highly important for precision agriculture and breeding and have been the subject of intensive research. However, the lack of publicly available high-quality image datasets with detailed annotations has severely hindered the development of these models. In this work, we present a comprehensive multicultivar and multiview rice plant image dataset (CVRP) created from 231 landraces and 50 modern cultivars grown under dense planting in paddy fields. The dataset includes images capturing rice plants in their natural environment, as well as indoor images focusing specifically on panicles, allowing for a detailed investigation of cultivar-specific differences. A semiautomatic annotation process using deep learning models was designed for annotations, followed by rigorous manual curation. We demonstrated the utility of the CVRP by evaluating the performance of four state-of-the-art (SOTA) semantic segmentation models. We also conducted 3D plant reconstruction with organ segmentation via images and annotations. The database not only facilitates general-purpose image-based panicle identification and segmentation but also provides valuable resources for challenging tasks such as automatic rice cultivar identification, panicle and grain counting, and 3D plant reconstruction. The database and the model for image annotation are available at https://bic.njau.edu.cn/CVRP.html.
Why it matches plant phenotyping methodsイネ画像データセットとアノテーションモデルを開発・評価し、セグメンテーション、器官再構成、穂・粒数計測などの再利用可能な表現型解析を中心に扱っているため。
abstractwe present a comprehensive multicultivar and multiview rice plant image dataset (CVRP)
Reproduction assets foundThe paper's own CVRP rice image dataset (images + annotations), accompanying code, and trained Mask2Former annotation model are explicitly stated as publicly available on Hugging Face and the authors' NJAU site.Dataset · publicThe CVRP dataset is publicly available on Hugging Face at https://huggingface.co/datasets/CVRPDataset/CVRP for academic use under the specified license.Open asset ↗CVRPDataset/CVRPhtml-lines:236-252Code · publicThe accompanying code and trained models are available at https://huggingface.co/CVRPDataset/Model.Open asset ↗CVRPDataset/Modelhtml-lines:236-252Code / dataset availability confirmedEurope PMC · checked 6 Sept 2026
The cuticle is a polymeric membrane covering all plant aerial organs of primary origin. It regulates water loss and defends against environmental stressors and pathogens. Despite its significance, understanding of the micro-mechanical properties of the cuticle (cuticular membrane; CM) remains limited. In this study, non-invasive Brillouin light scattering (BLS) spectroscopy was applied to probe the micro-mechanics of native CM, dewaxed CM (DCM), and isolated cutin matrix (CU) of mature apple fruit. The BLS signal arises from the photon interaction with thermally induced pressure waves and allows for imaging with mechanical contrast. The derived loss tangent showed significant differences with wax extraction from the CM and further with carbohydrate extraction from the DCM, consistent with tensile test results. Spatial heterogeneity between anticlinal and periclinal regions was observed by BLS microscopy of CM and DCM, but not in CU. The key conclusions are: (1) BLS is sensitive to micro-mechanical variations, particularly the strain-stiffening effect of the cutin framework, offering insights into the CM's micro-mechanical behavior and underlying chemical structures; (2) CM and DCM exhibit spatial micro-mechanical heterogeneity between periclinal and anticlinal regions.
Why it matches plant phenotyping methodsリンゴ果実のクチクラの微力学特性を、BLS顕微鏡による非侵襲的イメージングで測定・比較しており、植物器官の物性形質取得が研究の中心である。
abstractnon-invasive Brillouin light scattering (BLS) spectroscopy was applied to probe the micro-mechanics of native CM, dewaxed CM (DCM), and isolated cutin matrix (CU) of mature apple fruit.
Reproduction assets foundThe paper deposits its underlying Brillouin light scattering measurement data (primary and supplementary figures) in a public LUIS repository (DOI 10.25835/xvsi5g6m). The Brillouin analysis python script is only available on request, so it is not a public code asset.Dataset · publicThe underlying data for all the primary and Supplementary Figs. has been deposited in a publicly accessible repository [ https://doi.org/10.25835/xvsi5g6m ] 67 . Raw data may be obtained from the authors upon reasonable request.Open asset ↗10.25835/xvsi5g6mlines:177-254Code / dataset availability confirmedEurope PMC · checked 6 Sept 2026
Radopholus similis severely damages banana roots causing significant yield losses. Field screening for resistance is labor intensive and inconsistent due to environmental variation and mixed nematode populations. The screenhouse offers a controlled environment but is limited by the time needed for root development and variation in plant growth. We developed and validated a high-throughput in vitro method for phenotyping banana resistance to R. similis using sand-Murashige and Skoog (MS) media. Tissue culture plantlets grown in sterilized sand-MS were inoculated with 50 female R. similis after root development and nematodes extracted eight weeks after inoculation to calculate the reproduction factor (RF). Although RF values were higher for in vitro than in the screenhouse, accession responses showed similar trends under both conditions. The in vitro method was rapid, cost-effective with higher throughput, accelerating phenotyping and enabling rapid assessment of banana accessions for breeding programs. Some accessions responded differently to the two methods indicating that additional methods, such as root necrosis scores are important to confirm resistance. This study is the first in vitro-based demonstration of phenotyping for nematode resistance using modified sand-MS media with improved root development and pathogen interactions.
Why it matches plant phenotyping methodsバナナの線虫抵抗性という植物状態を評価する高スループットin vitroフェノタイピング法を開発・検証し、既存のスクリーンハウス法と比較しているため、方法が研究の中心である。
abstractWe developed and validated a high-throughput in vitro method for phenotyping banana resistance to R. similis using sand-Murashige and Skoog (MS) media.
Reproduction assets foundThe paper's Data Availability statement explicitly deposits the plant entry list, raw datasets, and generated/analyzed datasets (Extended data) for this banana R. similis resistance phenotyping study on Figshare under CC-BY 4.0, matching an allowed URL. No author analysis code was deposited.Dataset · publicThe list of all plant entries, raw datasets, and datasets generated during and/or analyzed during the current study (Extended data) referred to in the manuscript text as supplementary materials are publicly available in Figshare: High-throughput resistance phenotyping of banana ( Musa spp.) against Radopholus similis . https://doi.org/10.6084/m9.figshare.28787480.v3 . The dataset has a CC-BY 4.0 license applied.Open asset ↗Figshare · 10.6084/m9.figshare.28787480.v3lines:139-144Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
Soil imaging in the field and laboratory has greatly advanced our understanding of plant root systems. Soil fungi function as important plant symbionts and decomposers of complex organic material in soil environments. For fungal hyphae, however, the application of soil imaging remains scarce, limiting our understanding of hyphal systems in soil. This scarce application is partly due to the challenging development of a soil imaging device for hyphae: technical requirements to resolve fine hyphae (2-5 μm in diameter) are high, while the device cost must be low to facilitate sufficient deployment that can capture the high spatial heterogeneity of hyphal dynamics in soil. This protocol describes the do-it-yourself assembly and application of a low-cost high-resolution imaging device for observing hyphae in soil. The assembly of the open-source imaging device relies on many 3D-printed parts, reducing material costs to ca. 930 USD. The application of the imaging device yields soil profile images with a resolution of up to 0.52 μm px-1 (49000 dpi) within an observable volume of 70 × 210 × 1.5 mm. By repeatedly imaging a soil profile using the presented techniques, changes in the amount, distribution, and morphology of hyphae in soil can be observed and quantified.
Why it matches plant phenotyping methods土壌中の菌糸の量・分布・形態を画像から観察・定量する低コスト高解像度イメージング装置の組立・応用プロトコルであり、植物関連状態の取得手法が中心である。
abstractThis protocol describes the do-it-yourself assembly and application of a low-cost high-resolution imaging device for observing hyphae in soil.
Reproduction assets foundThe paper deposits its imaging-device design files, operating software, and high-resolution soil profile image sets on Zenodo, all paper-specific and publicly available.Dataset · publicerials and methods
The protocol described in this peer-reviewed article is published on protocols.io, https://dx.doi.org/10.17504/protocols.io.bp2l6xo3zlqe/v1 , and is included for printing as S1 File with this article. Furthermore, three sets of high-resolution images yielded following the protocol are available from Zenodo at https://doi.org/10.5281/zenodo.10730414 . The high-resolution images were acquired between May and October 2023 in a Quercus serrata grove at the Kansai Research Center of the Forestry and Forest Products Research Institute (FFPRI) in Kyoto City, Japan (34°56’N, 135°46’E). The grove was located on a Cambisol [ 44 ] in flat terrain. Monthly mean air temperature rangedOpen asset ↗Zenodo · 10.5281/zenodo.10730414lines:31-38Dataset · publicl.
The protocol is also available on protocols.io.
(PDF)
S1 Dataset
Set of soil profile images acquired at focus depths of 0, 0.025, and 0.05 mm.
Original images in the JPG format taken at an imaging resolution of 0.65 μm px -1 (39200 dpi).
(ZIP)
Data Availability Statement
All design files used to assemble the imaging device ( https://doi.org/10.5281/zenodo.10689905 ), all software to operate the imaging device ( https://doi.org/10.5281/zenodo.10815832 ), and several sets of images yielded with the imaging device ( https://doi.org/10.5281/zenodo.10730414 ) are available from the data repository Zenodo. All remaining data are within the manuscript and its Supporting Information files.Open asset ↗Zenodo · 10.5281/zenodo.10689905lines:147-155Code / dataset availability confirmedEurope PMC · checked 6 Sept 2026
Assessing the health status of vegetation is of vital importance for all stakeholders. Multi-spectral and hyper-spectral imaging systems are tools for evaluating the health of vegetation in laboratory settings, and also hold the potential of assessing vegetation of large portions of land. However, the literature lacks benchmark datasets to test algorithms for predicting plant health status, with most researchers creating tailored datasets. This work presents a dataset composed of multi-spectral images, hyper-spectral reflectance values, and measurements of weight, chlorophyll, and nitrogen content of leaves at five different drying stages, from avocado, olive, and grape trees, which are common crops in the Valparaíso region of Chile. This dataset is a valuable asset for developing tools in the field of precision agriculture and assessing the general health status of vegetation.
Why it matches plant phenotyping methods植物のマルチスペクトル・ハイパースペクトル画像と葉の水分状態・化学形質を含む評価用データセットを構築しており、フェノタイピング手法開発のためのベンチマークが中心である。
abstractThis work presents a dataset composed of multi-spectral images, hyper-spectral reflectance values, and measurements of weight, chlorophyll, and nitrogen content of leaves at five different drying stages
Reproduction assets foundThe paper's multispectral images, hyperspectral reflectance, and trait measurements (weight, chlorophyll, nitrogen, fuel moisture) are publicly deposited on Figshare with an explicit DOI. The authors' sample Matlab code is included within that dataset. The MicaSense imageprocessing repository is a generic third-party工具Dataset · publicAll the data is available at this repository DOI: https://doi.org/10.6084/m9.figshare.26950660.v2.Open asset ↗figshare · 10.6084/m9.figshare.26950660.v2pdf-page:14 lines:1-35Code / dataset availability confirmedCrossref · checked 14 Sept 2026
Agricultural productivity is increasingly threatened by plant diseases, which can spread rapidly and lead to significant crop losses if not identified early. Detecting plant diseases accurately in diverse and uncontrolled environments remains challenging, as most current detection methods rely heavily on lab-captured images that may not generalise well to real-world settings. This paper aims to develop models capable of accurately identifying plant diseases across diverse conditions, overcoming the limitations of existing methods. A combined dataset was utilised, incorporating the PlantDoc dataset with web-sourced images of plants from online platforms. State-of-the-art convolutional neural network (CNN) architectures, including EfficientNet-B0, EfficientNet-B3, ResNet50, and DenseNet201, were employed and fine-tuned for plant leaf disease classification. A key contribution of this work is the application of enhanced data augmentation techniques, such as adding Gaussian noise, to improve model generalisation. The results demonstrated varied performance across the datasets. When trained and tested on the PlantDoc dataset, EfficientNet-B3 achieved an accuracy of 73.31%. In cross-dataset evaluation, where the model was trained on PlantDoc and tested on a web-sourced dataset, EfficientNet-B3 reached 76.77% accuracy. The best performance was achieved with the combination of the PlanDoc and web-sourced datasets resulting in an accuracy of 80.19% indicating very good generalisation in diverse conditions. Class-wise F1-scores consistently exceeded 90% for diseases such as apple rust leaf and grape leaf across all models, demonstrating the effectiveness of this approach for plant disease detection.
Why it matches plant phenotyping methods植物葉の画像から病害状態を推定する深層学習手法の開発・汎化評価が中心であり、植物表現型（病徴・病害状態）の取得方法に該当する。
abstractThis paper aims to develop models capable of accurately identifying plant diseases across diverse conditions, overcoming the limitations of existing methods.
Reproduction assets foundThe paper's web-sourced plant disease image dataset (the paper-specific data contribution, combined with PlantDoc for experiments) is publicly deposited on Zenodo per the Data Availability Statement. PlantDoc is a cited third-party dataset, not a paper-specific asset, and no author analysis code or trained model is de-Dataset · publicData Availability Statement: Data used in paper are available at: https://zenodo.org/records/14051480Open asset ↗zenodo · 14051480pdf-page:21 lines:1-57Code / dataset availability confirmedEurope PMC · checked 6 Sept 2026
Rain cracking compromises quality and quantity of sweet cherries worldwide. Cracking susceptibility differs among genotypes. The objective was to (1) phenotype the progeny of a cross between a tolerant and a susceptible sweet cherry cultivar for cuticle mass per unit area, strain release on cuticle isolation, cuticular microcracking and calcium/dry mass ratio and (2) relate these characteristics to cracking susceptibilities evaluated in laboratory immersion assays and published multiyear field observations. Mass of the dewaxed cuticle per unit area and strain release upon cuticle isolation were significantly related to cracking susceptibility in lab or field. Cuticular microcracking in the stylar end region as indexed by infiltration with acridine orange was more severe in susceptible than in tolerant genotypes and significantly correlated with susceptibility to cracking in lab and field. The Ca/dry mass ratio was lower (-8%) for susceptible than for tolerant genotypes. Fruit that cracked early had less Ca than those that cracked later. Only the Ca/dry mass ratio of the stylar end region was significantly correlated with cracking susceptibility in the field. Based on stepwise regression analyses microcracking of the cuticle accounted for most of the cracking susceptibilities in field and lab (partial r2 = 0.331 to 0.338 for field vs. r2 = 0.326 to 0.453 for lab). The variability in cracking susceptibility accounted for increased to a r2 = 0.571 (lab) when adding mass of dewaxed cuticle, up to r2 = 0.421 (field) when adding the Ca/dry mass ratio in the stylar end region or up to r2 = 0.478 (field) when entering the strain release on isolation into the model. A protocol for phenotyping is suggested that allows larger progenies to be phenotyped for microcracking, DCM mass and strain release.
Why it matches plant phenotyping methodsサクランボ果実の微細亀裂、クチクラ質量、ひずみ解放などを用いた表現型評価を扱い、大規模後代を評価するためのフェノタイピングプロトコルを提案しているため、方法が中心的である。
abstractThe objective was to (1) phenotype the progeny of a cross between a tolerant and a susceptible sweet cherry cultivar for cuticle mass per unit area, strain release on cuticle isolation, cuticular microcracking and calcium/dry mass ratio and (2) relate these characteristics to cracking susceptibilities evaluated in laboratory immersion assays and published multiyear field observations.
Reproduction assets foundThe paper's supporting information S1 Dataset contains the raw phenotyping data (cracking susceptibility, cuticle mass, strain release, microcracking, Ca/dry mass ratios) underlying all figures, publicly available as an XLSX supplement on the PLOS ONE article page. No author analysis code or trained models are reportedDataset · publicS1 Dataset. The raw data of all figures and the data on mean fruit mass of the individual genotypes are available in the S1 Dataset.Open asset ↗lines:305-314Code / dataset availability confirmedbioRxiv · Europe PMC · checked 15 Sept 2026
Field / plotLaboratory / benchtopX-ray / CTRootWhole plant / canopy / plot / field
Soil compaction and escalating global drought increase soil strength and stiffness. It remains unclear which plant root biomechanical mechanisms/traits enable growth in these harsh conditions. Here, we combine synchrotron X-ray computed tomography with spatially resolved X-ray diffraction to characterize the biomechanics of a replica root-soil system. We map the strain field around the root tip, finding strong agreement with finite element simulations, thereby demonstrating a promising new in-vivo measurement protocol.
Why it matches plant phenotyping methods根周辺のひずみ場という根の力学的形質を、X線CT・回折と有限要素解析で測定・検証する新規プロトコルが研究の中心である。
abstractWe map the strain field around the root tip, finding strong agreement with finite element simulations, thereby demonstrating a promising new in-vivo measurement protocol.
Reproduction assets foundThe paper deposits its X-ray diffraction and X-ray imaging (XCT) measurements in the Southampton Pure repository (DOI 10.5258/SOTON/D3309.274) and its processing scripts in a companion deposit (DOI 10.5258/SOTON/D3309.276), both with explicit availability statements and public URLs.Dataset · public∇uT ), F(σ′) > 0,x ∈ Ω
σ′ = Cep
: (∇u+∇uT ), F(σ′) = 0,x ∈ Ω
u·ê1 = 0, x ∈ ΓAxis
u = 0, x ∈ ΓC,Top
u = [0,wstep]T , x ∈ Γbot ∪Γout
n̂·∇u = 0, x ∈ Γtop ∪ΓC,tip
n̂·σ = ppen, x ∈ (Γtop ∩Ω∩Ωc)∪(ΓC,tip ∩Ω∩Ωc)
. (29)
Data Records
273
All X-ray diffraction and X-ray imaging data used in this study can be found in the Pure repository: https://doi.org/10.5258/SOTON/D3309.274
Code availability
275
All scripts used to process the data can be found in the Pure repository: https://doi.org/10.5258/SOTON/D3309.276
References
277
1. Lee, H. et al. Ipcc, 2023: Climate change 2023: Synthesis report, summary for policymakers. contribution of working
278
groups i, ii and iii to the sixth assessment report ofOpen asset ↗Pure repository · 10.5258/SOTON/D3309.274pdf-raw-page:9 lines:1-96Code · publicu = 0, x ∈ Γtop ∪ΓC,tip
n̂·σ = ppen, x ∈ (Γtop ∩Ω∩Ωc)∪(ΓC,tip ∩Ω∩Ωc)
. (29)
Data Records
273
All X-ray diffraction and X-ray imaging data used in this study can be found in the Pure repository: https://doi.org/10.5258/SOTON/D3309.274
Code availability
275
All scripts used to process the data can be found in the Pure repository: https://doi.org/10.5258/SOTON/D3309.276
References
277
1. Lee, H. et al. Ipcc, 2023: Climate change 2023: Synthesis report, summary for policymakers. contribution of working
278
groups i, ii and iii to the sixth assessment report of the intergovernmental panel on climate change [core writing team, h.
279
lee and j. romero (eds.)]. ipcc, geneva, switzerland. (2023).
2Open asset ↗Pure repository · 10.5258/SOTON/D3309.276pdf-raw-page:9 lines:1-96Code / dataset availability confirmedCrossref · Europe PMC · checked 14 Sept 2026
Abstract BerryPortraits (Phenotyping of Ripening Traits) is open source Python-based image-analysis software that rapidly detects and segments berries and extracts morphometric data on fruit quality traits such as berry color, size, shape, and uniformity. Utilizing the YOLOv8 framework and community-developed, actively-maintained Python libraries such as OpenCV, BerryPortraits software was trained on 512 postharvest images (taken under controlled lighting conditions) of phenotypically diverse cranberry populations ( Vaccinium macrocarpon Ait.) from the two largest public cranberry breeding programs in the U.S. The implementation of CIELAB, an intuitive and perceptually uniform color space, enables differentiation between berry color and berry brightness, which are confounded in classic RGB color channel measurements. Furthermore, computer vision enables precise and quantifiable color phenotyping, thus facilitating inclusion of researchers and data analysts with color vision deficiency. BerryPortraits is a phenotyping tool for researchers in plant breeding, plant genetics, horticulture, food science, plant physiology, plant pathology, and related fields. BerryPortraits has strong potential applications for other specialty crops such as blueberry, lingonberry, caneberry, grape, and more. As an open source phenotyping tool based on widely-used python libraries, BerryPortraits allows anyone to use, fork, modify, optimize, and embed this software into other tools or pipelines.
Why it matches plant phenotyping methods植物果実の色・サイズ・形状・均一性を画像から抽出するオープンソースの表現型解析ソフトウェアを開発しており、植物フェノタイピング手法が研究の中心である。
abstractBerryPortraits (Phenotyping of Ripening Traits) is open source Python-based image-analysis software that rapidly detects and segments berries and extracts morphometric data on fruit quality traits such as berry color, size, shape, and uniformity.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicHere we present BerryPortraits: Phenotyping Of Ripening Traits [‘with Rapid Automated Imaging Tools and Software’, for those disinclined towards brevity]) ( https://github.com/Breeding-Insight/BerryPortraits/ )Open asset ↗Breeding-Insight/BerryPortraitslines:100-105Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
Pollen is becoming an increasingly important subject for molecular researchers in genetic engineering, plant breeding, and environmental monitoring. To broaden the scope of these studies, it is essential to develop accessible methods for scientists who are not specialized in palynology. The article presents a simplified technical procedure for preparing pollen grains for scanning electron microscopy (SEM). The protocol is convenient for any molecular laboratory due to its small set of reagents, ease of execution, low cost, does not require special equipment, and takes only one hour to complete. The high penetrating ability of formaldehyde and the final delicate dehydration using hexamethyldisilazane (HMDS) instead of critical point drying allow for sufficient preservation of the architecture of the aperture, which is considered a gateway for the passage of biomolecules. The method was successfully applied to pollen grains of representatives of dicotyledons (beetroot, petunia, radish, tomato and tobacco) and monocotyledons (lily, onion, corn, rye and wheat). Species studied included insect-pollinated (entomophilous) and wind-pollinated (anemophilous) species. A comparative analysis of the sizes of fresh living pollen grains under a light microscope and those prepared for SEM showed some shrinkage. Quantitative analysis of the degree of pollen grain shrinkage showed that this process depends on the initial shape of dry pollen grains, and the number and structure of apertures. The results support the theoretical model of the folding/unfolding pathways of pollen grains.
Why it matches plant phenotyping methods植物花粉のSEM観察用試料調製法そのものを開発し、複数植物で適用・比較検証しているため、形態計測に関する中心的な方法論研究である。
abstractThe article presents a simplified technical procedure for preparing pollen grains for scanning electron microscopy (SEM).
Reproduction assets foundThe paper's quantitative pollen shrinkage measurements (Table S1) and light microscopy images (Figures S3–S4) are contained in the publicly downloadable MDPI Supplementary Materials, which directly reproduce this paper's phenotyping measurements. No author analysis code or trained models are mentioned.Supplement · publicoly Bogdanov—at the department of electron microscopy, Lomonosov Moscow State University.
Abbreviations
The following abbreviations are used in this manuscript:
SEM
Scanning Electron Microscopy
HMDS
Hexamethyldisilazane
SA
Short axis
LA
Long axis
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/plants13152140/s1 , Figure S1: The order of steps for pollen preparation according to the developed protocol; Figure S2: Scheme of measured pollen grain diameters; Figure S3: Light microscopy of pollen grains of insect-pollinated species; Figure S4: Light microscopy of pollen grains of wind-pollinated species; Table S1: Comparison Open asset ↗lines:98-127Code / dataset availability confirmedarXiv · OpenAlex · checked 13 Sept 2026
Potato yield is an important metric for farmers to further optimize their cultivation practices. Potato yield can be estimated on a harvester using an RGB-D camera that can estimate the three-dimensional (3D) volume of individual potato tubers. A challenge, however, is that the 3D shape derived from RGB-D images is only partially completed, underestimating the actual volume. To address this issue, we developed a 3D shape completion network, called CoRe++, which can complete the 3D shape from RGB-D images. CoRe++ is a deep learning network that consists of a convolutional encoder and a decoder. The encoder compresses RGB-D images into latent vectors that are used by the decoder to complete the 3D shape using the deep signed distance field network (DeepSDF). To evaluate our CoRe++ network, we collected partial and complete 3D point clouds of 339 potato tubers on an operational harvester in Japan. On the 1425 RGB-D images in the test set (representing 51 unique potato tubers), our network achieved a completion accuracy of 2.8 mm on average. For volumetric estimation, the root mean squared error (RMSE) was 22.6 ml, and this was better than the RMSE of the linear regression (31.1 ml) and the base model (36.9 ml). We found that the RMSE can be further reduced to 18.2 ml when performing the 3D shape completion in the center of the RGB-D image. With an average 3D shape completion time of 10 milliseconds per tuber, we can conclude that CoRe++ is both fast and accurate enough to be implemented on an operational harvester for high-throughput potato yield estimation. CoRe++'s high-throughput and accurate processing allows it to be applied to other tuber, fruit and vegetable crops, thereby enabling versatile, accurate and real-time yield monitoring in precision agriculture. Our code, network weights and dataset are publicly available at https://github.com/UTokyo-FieldPhenomics-Lab/corepp.git.
Why it matches plant phenotyping methodsRGB-D画像からジャガイモ塊茎の3D形状を補完し、体積・収量を推定する手法を開発・検証しており、植物フェノタイピング手法が研究の中心である。
abstractwe developed a 3D shape completion network, called CoRe++, which can complete the 3D shape from RGB-D images.
Reproduction assets foundThe paper's abstract explicitly states that the authors' code, network weights, and the potato tuber RGB-D/3D point cloud dataset are publicly available at the authors' GitHub repository (UTokyo-FieldPhenomics-Lab/corepp), which is a paper-specific, public, actionable asset for the CoRe++ phenotyping analysis.Code · publicOur code, network weights and dataset are publicly available at https://github.com/UTokyo-FieldPhenomics-Lab/corepp.git .Open asset ↗UTokyo-FieldPhenomics-Lab/corepplines:1-93Code / dataset availability confirmedOpenAlex · Europe PMC · bioRxiv · checked 15 Sept 2026
Abstract The need for more sustainable agricultural systems is becoming increasingly apparent. The global demand for agricultural products — food, feed, fuel and fiber — will continue to increase as the global population continues to grow. This challenge is compounded by climate change. Not only does a changing climate make it difficult to maintain stable yields but current agricultural systems are a major source of greenhouse gas emissions and continue to drive the problem further. Therefore, future agricultural systems must not only increase production but also significantly decrease negative environmental impacts. One approach to addressing this is to begin breeding and cultivating new plant species that have fundamental sustainability advantages over our existing crops. The Lemnaceae, a.k.a duckweeds, are one such species that have potential to increase output and reduce the negative environmental impacts of agricultural production. Herein we describe the Automated Lab-scale PHenotyping Apparatus, ALPHA, for high-throughput phenotyping of Lemnaceae. ALPHA is being used for selective breeding of one species, Lemna gibba , toward the goal of creating a new crop for use in sustainable agricultural systems. ALPHA can be used on many small aquatic plant species to assess growth rates in different environmental conditions. A proof of principle use case is demonstrated where ALPHA is used to determine saltwater tolerance of 6 different varieties of L. gibba .
Why it matches plant phenotyping methods小型水生植物の成長率を高スループットに定量する自動フェノタイピング装置を開発・実証しており、表現型取得法が研究の中心です。
abstractHerein we describe the Automated Lab-scale PHenotyping Apparatus, ALPHA, for high-throughput phenotyping of Lemnaceae.
Reproduction assets foundThe authors state that all source code for the phenotyping system, the PlantCV image analysis pipeline, the R growth-curve analysis, 3D models, and the data generated for this study (including PlantCV_Output_Salinity.csv and Barcode_Sample_Map.csv) are publicly available in the ALPHA GitHub repository.Code · publicAll source code used in the phenotyping system, 3D models for printed parts and data generated
for this study are available in the ALPHA Github repository.Open asset ↗pdf-raw-page:2 lines:1-49Dataset · publicThis code requires data output from the quantification pipeline
“PlantCV_Output_Salinity.csv” and the barcode map “Barcode_Sample_Map.csv”. Both are also
available in the Github repository.Open asset ↗pdf-raw-page:7 lines:1-33Code / dataset availability confirmedarXiv · checked 14 Sept 2026
As the world population is expected to reach 10 billion by 2050, our agricultural production system needs to double its productivity despite a decline of human workforce in the agricultural sector. Autonomous robotic systems are one promising pathway to increase productivity by taking over labor-intensive manual tasks like fruit picking. To be effective, such systems need to monitor and interact with plants and fruits precisely, which is challenging due to the cluttered nature of agricultural environments causing, for example, strong occlusions. Thus, being able to estimate the complete 3D shapes of objects in presence of occlusions is crucial for automating operations such as fruit harvesting. In this paper, we propose the first publicly available 3D shape completion dataset for agricultural vision systems. We provide an RGB-D dataset for estimating the 3D shape of fruits. Specifically, our dataset contains RGB-D frames of single sweet peppers in lab conditions but also in a commercial greenhouse. For each fruit, we additionally collected high-precision point clouds that we use as ground truth. For acquiring the ground truth shape, we developed a measuring process that allows us to record data of real sweet pepper plants, both in the lab and in the greenhouse with high precision, and determine the shape of the sensed fruits. We release our dataset, consisting of almost 7,000 RGB-D frames belonging to more than 100 different fruits. We provide segmented RGB-D frames, with camera intrinsics to easily obtain colored point clouds, together with the corresponding high-precision, occlusion-free point clouds obtained with a high-precision laser scanner. We additionally enable evaluation of shape completion approaches on a hidden test set through a public challenge on a benchmark server.
Why it matches plant phenotyping methods果実の3D形状という植物器官の形態形質を対象に、RGB-D画像・高精度点群・評価用ベンチマークを構築しており、形状取得と推定の方法論が中心である。
abstractWe provide an RGB-D dataset for estimating the 3D shape of fruits.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicOur development toolkit including a data loader is available at:
https://github.com/PRBonn/shape_completion_toolkit for handling the dataset and computing metrics.Open asset ↗PRBonn/shape_completion_toolkitlines:55-81Code / dataset availability confirmedCrossref · Europe PMC · checked 15 Sept 2026
ABSTRACT Plant protoplasts provide starting material for of inducing pluripotent cell masses that are competent for tissue regeneration in vitro, analogous to animal induced pluripotent stem cells (iPSCs). Dedifferentiation is associated with large-scale chromatin reorganisation and massive transcriptome reprogramming, characterised by stochastic gene expression. How this cellular variability reflects on chromatin organisation in individual cells and what factors influence chromatin transitions during culturing are largely unknown. Here, we used high-throughput imaging and a custom supervised image analysis protocol extracting over 100 chromatin features of cultured protoplasts. The analysis revealed rapid, multiscale dynamics of chromatin patterns with a trajectory that strongly depended on nutrient availability. Decreased abundance in H1 (linker histones) is hallmark of chromatin transitions. We measured a high heterogeneity of chromatin patterns indicating intrinsic entropy as a hallmark of the initial cultures. We further measured an entropy decline over time, and an antagonistic influence by external and intrinsic factors, such as phytohormones and epigenetic modifiers, respectively. Collectively, our study benchmarks an approach to understand the variability and evolution of chromatin patterns underlying plant cell reprogramming in vitro.
Why it matches plant phenotyping methods植物プロトプラストのクロマチン状態を高スループット画像とカスタム画像解析で定量し、100以上の特徴を抽出・ベンチマークしており、表現型取得法が研究の中心である。
abstractwe used high-throughput imaging and a custom supervised image analysis protocol extracting over 100 chromatin features of cultured protoplasts.
Reproduction assets foundThe paper's chromatin feature datasets (Dryad doi:10.5061/dryad.pnvx0k6wp) and images (BioStudies S-BIAD1157) are paper-specific public assets, but their repository URLs are not among the allowed URLs, so they cannot be listed. The authors' adapted entropy analysis script is publicly available on the authors' GitHub (aCode · publicinterval (a new observation from the same group will fall inside the ellipse with probability P= 0.95).
Entropy analysis
The initial script for computing Shannon Entropy is described in Dussiau et al. (2022) and is available at https://osf.io/9mcwg/ . The adapted script for computing entropy of chromatin features is provided at https://github.com/barouxlab/ChromatinEntropy . When all cells (segmented nuclei) express the same value for a given feature, this entropy of the feature will be null. The more cell-to-cell variability for a given chromatin feature, the higher value of entropy.
Plots and statistical tests
Box plots, violin plots, scatter plots, 2D contours and histograms were created Open asset ↗barouxlab/ChromatinEntropylines:121-147Code / dataset availability confirmedOpenAlex · Crossref · Europe PMC · checked 7 Sept 2026
BACKGROUND: Image-based crop growth modeling can substantially contribute to precision agriculture by revealing spatial crop development over time, which allows an early and location-specific estimation of relevant future plant traits, such as leaf area or biomass. A prerequisite for realistic and sharp crop image generation is the integration of multiple growth-influencing conditions in a model, such as an image of an initial growth stage, the associated growth time, and further information about the field treatment. While image-based models provide more flexibility for crop growth modeling than process-based models, there is still a significant research gap in the comprehensive integration of various growth-influencing conditions. Further exploration and investigation are needed to address this gap. METHODS: We present a two-stage framework consisting first of an image generation model and second of a growth estimation model, independently trained. The image generation model is a conditional Wasserstein generative adversarial network (CWGAN). In the generator of this model, conditional batch normalization (CBN) is used to integrate conditions of different types along with the input image. This allows the model to generate time-varying artificial images dependent on multiple influencing factors. These images are used by the second part of the framework for plant phenotyping by deriving plant-specific traits and comparing them with those of non-artificial (real) reference images. In addition, image quality is evaluated using multi-scale structural similarity (MS-SSIM), learned perceptual image patch similarity (LPIPS), and Fréchet inception distance (FID). During inference, the framework allows image generation for any combination of conditions used in training; we call this generation data-driven crop growth simulation. RESULTS: Experiments are performed on three datasets of different complexity. These datasets include the laboratory plant Arabidopsis thaliana (Arabidopsis) and crops grown under real field conditions, namely cauliflower (GrowliFlower) and crop mixtures consisting of faba bean and spring wheat (MixedCrop). In all cases, the framework allows realistic, sharp image generations with a slight loss of quality from short-term to long-term predictions. For MixedCrop grown under varying treatments (different cultivars, sowing densities), the results show that adding these treatment information increases the generation quality and phenotyping accuracy measured by the estimated biomass. Simulations of varying growth-influencing conditions performed with the trained framework provide valuable insights into how such factors relate to crop appearances, which is particularly useful in complex, less explored crop mixture systems. Further results show that adding process-based simulated biomass as a condition increases the accuracy of the derived phenotypic traits from the predicted images. This demonstrates the potential of our framework to serve as an interface between a data-driven and a process-based crop growth model. CONCLUSION: The realistic generation and simulation of future plant appearances is adequately feasible by multi-conditional CWGAN. The presented framework complements process-based models and overcomes their limitations, such as the reliance on assumptions and the low exact field-localization specificity, by realistic visualizations of the spatial crop development that directly lead to a high explainability of the model predictions.
Why it matches plant phenotyping methods植物画像を生成し、そこから植物個体別形質を推定する二段階の画像ベース表現型解析フレームワークを開発・評価しており、表現型取得・推定手法が研究の中心である。
abstractWe present a two-stage framework consisting first of an image generation model and second of a growth estimation model, independently trained.
Reproduction assets foundThe paper's authors explicitly state that source code and links to the phenotyping datasets (Arabidopsis, GrowliFlower, MixedCrop) are publicly available in their GitHub repository, which implements the multi-conditional CWGAN crop growth simulation and growth estimation framework.Code · publicSource code and links to the datasets are publicly available at https://github.com/luked12/crop-growth-cgan .Open asset ↗luked12/crop-growth-cganlines:216-253Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
Hyperspectral imaging allows for rapid, non-destructive and objective assessments of crop health. Narrowband-hyperspectral data was used to select wavelength regions that can be exploited to identify wheat infected with soil-borne mosaic virus. First, leaf samples were scanned in the lab to investigate spectral differences between healthy and diseased leaves, including non-symptomatic and symptomatic areas within a diseased leaf. The potential of 84 commonly used vegetation indices to find infection was explored. A machine-learning approach was used to create a classification model to automatically separate pixels into symptomatic, non-symptomatic and healthy classes. The success rate of the model was 69.7% using the full spectrum. It was very encouraging that by using a subset of only four broad bands, sampled to simulate a data set from a much simpler and less costly multispectral camera, accuracy increased to 71.3%. Next, the classification models were validated on field data. Infection in the field was successfully identified using classifiers trained on the entire spectrum of the hyperspectral data acquired in a lab setting, with the best accuracy being 64.9%. Using a subset of wavelengths, simulating multispectral data, the accuracy dropped by only 3 percentage points to 61.9%. This research shows the potential of using lab scans to train classifiers to be successfully applied in the field, even when simultaneously reducing the hyperspectral data to multispectral data.
Why it matches plant phenotyping methods小麦の感染状態をハイパースペクトル画像から推定する分類手法を開発し、実験室データで学習したモデルを圃場データで検証しているため、植物フェノタイピング手法が中心である。
abstractA machine-learning approach was used to create a classification model to automatically separate pixels into symptomatic, non-symptomatic and healthy classes.
Reproduction assets foundThe paper's hyperspectral lab/field wheat scan datasets are publicly deposited in OSU Scholars Archive (DOI 10.7267/z316q855z). Code is only available upon request, so it does not qualify as a public asset.Dataset · publicntal Monitoring Programs
(CTEMPs); and Collaborative Research; CompSustNet: Expanding the Horizons of Computational Sustain-
ability, respectively).
Availability of data and material The datasets generated during and/or analyzed during the current study are
available in the Oregon State University’s Scholars Archive repository, https://doi.org/10.7267/z316q855z.Code availability Code will be made available upon request.
Declarations
Conflicts of interest/competing interests The authors declare that they have no conflict of interest.
Open Access This article is licensed under a Creative CommonsAttribution 4.0 International License, which
permits use, sharing, adaptation, distribution aOpen asset ↗Oregon State University’s Scholars Archive · 10.7267/z316q855zpdf-raw-page:17 lines:1-41Code / dataset availability confirmedEurope PMC · checked 7 Sept 2026
Background Plants are known to be infected by a wide range of pathogenic microbes. To study plant diseases caused by microbes, it is imperative to be able to monitor disease symptoms and microbial colonization in a quantitative and objective manner. In contrast to more traditional measures that use manual assignments of disease categories, image processing provides a more accurate and objective quantification of plant disease symptoms. Besides monitoring disease symptoms, computational image processing provides additional information on the spatial localization of pathogenic microbes in different plant tissues. Results Here we report on an image analysis tool called ScAnalyzer to monitor disease symptoms and bacterial spread in Arabidopsis thaliana leaves. Thereto, detached leaves are assembled in a grid and scanned, which enables automated separation of individual samples. A pixel color threshold is used to segment healthy (green) from chlorotic (yellow) leaf areas. The spread of luminescence-tagged bacteria is monitored via light-sensitive films, which are processed in a similar manner as the leaf scans. We show that this tool is able to capture previously identified differences in susceptibility of the model plant A. thaliana to the bacterial pathogen Xanthomonas campestris pv. campestris. Moreover, we show that the ScAnalyzer pipeline provides a more detailed assessment of bacterial spread within plant leaves than previously used methods. Finally, by combining the disease symptom values with bacterial spread values from the same leaves, we show that bacterial spread precedes visual disease symptoms. Conclusion Taken together, we present an automated script to monitor plant disease symptoms and microbial spread in A. thaliana leaves. The freely available software ( https://github.com/MolPlantPathology/ScAnalyzer ) has the potential to standardize the analysis of disease assays between different groups.
Why it matches plant phenotyping methods植物葉の病徴と病原体拡散を画像処理で定量化するツールおよび解析パイプラインが研究の中心であり、植物の病害状態を直接推定するため。
abstractimage processing provides a more accurate and objective quantification of plant disease symptoms.
Reproduction assets foundThe paper's ScAnalyzer Python/R analysis pipeline and the raw leaf/luminescence images are publicly available on the authors' GitHub repository, along with the printable leaf-grid sheet used for phenotyping.Code · publicThe code is available on GitHub ( https://github.com/MolPlantPathology/ScAnalyzer ).Open asset ↗MolPlantPathology/ScAnalyzerlines:124-131Code / dataset availability confirmedOpenAlex · Crossref · checked 7 Sept 2026
Phenotyping of genetic resources is an important prerequisite for the selection of resistant varieties in breeding programs and research. Computer vision techniques have proven to be a useful tool for digital phenotyping of diseases of interest. One pathogen that is increasingly observed in Europe is Diplocarpon coronariae, which causes apple blotch disease. In this study, a high-throughput phenotyping method was established to evaluate genetic apple resources for susceptibility to D. coronariae. For this purpose, inoculation trials with D. coronariae were performed in a laboratory and images of infested leaves were taken 7, 9 and 13 days post inoculation. A pre-trained YOLOv5s model was chosen to establish the model, which was trained with an image dataset of 927 RGB images. The images had a size of 768 × 768 pixels and were divided into 738 annotated training images, 78 validation images and 111 background images without symptoms. The accuracy of symptom prediction with the trained model was 95%. These results indicate that our model can accurately and efficiently detect spots with acervuli on detached apple leaves. Object detection can therefore be used for digital phenotyping of detached leaf assays to assess the susceptibility to D. coronariae in a laboratory.
Why it matches plant phenotyping methodsリンゴ葉の病斑をYOLOv5で画像から検出し、病害感受性を評価する高スループット表現型計測法を確立・検証しており、フェノタイピング手法が中心である。
abstractIn this study, a high-throughput phenotyping method was established to evaluate genetic apple resources for susceptibility to D. coronariae.
Reproduction assets foundThe authors explicitly state that the image dataset used for model training (image_dataset_2023, 927 RGB images with 4167 annotations) and the YOLOv5s detection workflow with instructions are available in an open-source GitHub repository. This is a paper-specific, public, actionable asset directly reproducing the phenyDataset · publicThe image dataset for the model training is available in the open-source
GitHub repository (https://github.com/digijkizo/Apple_blotch_detection/tree/master,
accessed on 29 April 2024).Open asset ↗https://github.com/digijkizo/Apple_blotch_detection/tree/masterpdf-page:5 lines:1-59Code · publicThe image dataset for the model training and the detection workflow
with instructions are available in the open-source GitHub repository (https://github.com/digijkizo/
Apple_blotch_detection/tree/master, accessed on 29 April 2024).Open asset ↗pdf-page:10 lines:1-59Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Premise Poikilohydric plants respond to hydration by undergoing dry-wet-dry cycles. Carbon balance represents the net gain or loss of carbon from each cycle. Here we present the first standard protocol for measuring carbon balance, including a custom-modified chamber system for infrared gas analysis, 12-h continuous monitoring, resolution of plant-substrate relationships, and in-chamber specimen hydration. Methods and results We applied the carbon balance technique to capture responses to water stress in populations of the moss Syntrichia caninervis , comparing 19 associated physiological variables. Carbon balance was negative in desiccation-acclimated (field-collected) mosses, which exhibited large respiratory losses. Contrastingly, carbon balance was positive in hydration-acclimated (lab-cultivated) mosses, which began exhibiting net carbon uptake Conclusions Carbon balance is a functional trait indicative of physiological performance, hydration stress, and survival in poikilohydric plants, and the carbon balance method can be applied broadly across taxa to test hypotheses related to environmental stress and global change.
Why it matches plant phenotyping methodsコケ植物の炭素収支を測定する標準プロトコルとカスタムチャンバーを開発し、炭素収支を機能形質として評価しているため、植物フェノタイピング手法が中心である。
abstractHere we present the first standard protocol for measuring carbon balance, including a custom-modified chamber system for infrared gas analysis, 12-h continuous monitoring, resolution of plant-substrate relationships, and in-chamber specimen hydration.
Reproduction assets foundThe authors deposit all case-study data and analysis materials in a public GitHub repository, explicitly stated in the Data Availability Statement. The R Markdown/R analysis workflow (Appendix S3) and supporting files are also provided, making the paper's carbon-balance phenotyping data and computational analysis code,Code · publiclability Statement
A detailed carbon balance protocol, RMD file, custom chamber baseplate data files, and standard curve data are available in the Supporting Information for this manuscript. All other data used in the manuscript, including in the hydration‐acclimation case study, are available via the public GitHub repository ( https://github.com/KirstenKCoe/Coe-et-al.-2024-APPS ).Open asset ↗KirstenKCoe/Coe-et-al.-2024-APPSlines:474-476Code / dataset availability confirmedCrossref · checked 7 Sept 2026
Accurate retrieval of canopy nutrient content has been made possible using visible-to-shortwave infrared (VSWIR) imaging spectroscopy. While this strategy has often been tested on closed green plant canopies, little is known about how nutrient content estimates perform when applied to pixels not dominated by photosynthetic vegetation (PV). In such cases, contributions of bare soil (BS) and non-photosynthetic vegetation (NPV), may significantly and nonlinearly reduce the spectral features relied upon for nutrient content retrieval. We attempted to define the loss of prediction accuracy under reduced PV fractional cover levels. To do so, we utilized VSWIR imaging spectroscopy data from the Global Airborne Observatory (GAO) and a large collection of lab-calibrated field samples of nitrogen (N) content collected across numerous crop species grown in several farming regions of the United States. Fractional cover values of PV, NPV, and BS were estimated from the GAO data using the Automated Monte Carlo Unmixing algorithm (AutoMCU). Errors in prediction from a partial least squares N model applied to the spectral data were examined in relation to the fractional cover of the unmixed components. We found that the most important factor in the accuracy of the partial least squares regression (PLSR) model is the fraction of photosynthetic vegetation (PV) cover, with pixels greater than 60% cover performing at the optimal level, where the coefficient of determination (R2) peaks to 0.66 for PV fractions of more than 60% and bare soil (BS) fractions of less than 20%. Our findings guide future spaceborne imaging spectroscopy missions as applied to agricultural cropland N monitoring.
Why it matches plant phenotyping methodsVSWIR画像分光とスペクトル混合分解・PLSRを用いて作物キャノピー窒素含量の推定精度を検証しており、植物形質取得法が研究の中心である。
abstractAccurate retrieval of canopy nutrient content has been made possible using visible-to-shortwave infrared (VSWIR) imaging spectroscopy.
Reproduction assets foundThe authors' PLSR nitrogen-retrieval Python code is publicly available on GitHub (NitrogenRetrieval repository) and archived on Zenodo (10.5281/zenodo.7967292). The AutoMCU code, airborne imaging spectroscopy data, and spectral reflectance data are only available by request from the corresponding author, so those are 'Code · publicAdditional
details regarding the algorithm employed for N retrieval and the corresponding Python
code can be found in the NitrogenRetrieval repository on our GitHub page, accessible at
the following URL: https://github.com/CMLandOcean/NitrogenRetrievalOpen asset ↗CMLandOcean/NitrogenRetrievalpdf-page:8 lines:1-56Code / dataset availability confirmedEurope PMC · checked 7 Sept 2026
Image segmentation is commonly used to estimate the location and shape of plants and their external structures. Segmentation masks are then used to localize landmarks of interest and compute other geometric features that correspond to the plant's phenotype. Despite its prevalence, segmentation-based approaches are laborious (requiring extensive annotation to train) and error-prone (derived geometric features are sensitive to instance mask integrity). Here, we present a segmentation-free approach that leverages deep learning-based landmark detection and grouping, also known as pose estimation. We use a tool originally developed for animal motion capture called SLEAP (Social LEAP Estimates Animal Poses) to automate the detection of distinct morphological landmarks on plant roots. Using a gel cylinder imaging system across multiple species, we show that our approach can reliably and efficiently recover root system topology at high accuracy, few annotated samples, and faster speed than segmentation-based approaches. In order to make use of this landmark-based representation for root phenotyping, we developed a Python library ( sleap-roots ) for trait extraction directly comparable to existing segmentation-based analysis software. We show that pose-derived root traits are highly accurate and can be used for common downstream tasks including genotype classification and unsupervised trait mapping. Altogether, this work establishes the validity and advantages of pose estimation-based plant phenotyping. To facilitate adoption of this easy-to-use tool and to encourage further development, we make sleap-roots , all training data, models, and trait extraction code available at: https://github.com/talmolab/sleap-roots and https://osf.io/k7j9g/.
Why it matches plant phenotyping methods根系のランドマーク検出・形状復元・形質抽出を行う深層学習ベースの植物フェノタイピング手法を開発・検証し、専用ライブラリも提供しているため。
abstractHere, we present a segmentation-free approach that leverages deep learning-based landmark detection and grouping, also known as pose estimation.
Reproduction assets foundThe authors explicitly make all paper-specific assets public: the sleap-roots trait-extraction codebase on GitHub, a separate repository with figure-replication code, and an OSF deposit containing labeled training data, trained pose-estimation models, and analysis files for the root phenotyping measurements.Code · publicthe specific code utilized for replicating the figures presented in this study can be found in a separate GitHub repository here: https://github.com/talmolab/Berrigan_et_al_sleap-rootsOpen asset ↗talmolab/Berrigan_et_al_sleap-roots · Berrigan_et_al_sleap-rootslines:485-526Dataset · publicThe datasets generated and/or analyzed during the current study are available in the Open Science Framework (OSF) repository. This includes the labeled data, predictive models, and analysis files, which can be accessed via the following link: https://osf.io/k7j9g/Open asset ↗osf.io/k7j9g · k7j9glines:485-526Code / dataset availability confirmedOpenAlex · Crossref · Europe PMC · checked 7 Sept 2026
BACKGROUND: Plant scientists have largely relied on pathogen growth assays and/or transcript analysis of stress-responsive genes for quantification of disease severity and susceptibility. These methods are destructive to plants, labor-intensive, and time-consuming, thereby limiting their application in real-time, large-scale studies. Image-based plant phenotyping is an alternative approach that enables automated measurement of various symptoms. However, most of the currently available plant image analysis tools require specific hardware platform and vendor specific software packages, and thus, are not suited for researchers who are not primarily focused on plant phenotyping. In this study, we aimed to develop a digital phenotyping tool to enhance the speed, accuracy, and reliability of disease quantification in Arabidopsis. RESULTS: Here, we present the Arabidopsis Disease Quantification (AraDQ) image analysis tool for examination of flood-inoculated Arabidopsis seedlings grown on plates containing plant growth media. It is a cross-platform application program with a user-friendly graphical interface that contains highly accurate deep neural networks for object detection and segmentation. The only prerequisite is that the input image should contain a fixed-sized 24-color balance card placed next to the objects of interest on a white background to ensure reliable and reproducible results, regardless of the image acquisition method. The image processing pipeline automatically calculates 10 different colors and morphological parameters for individual seedlings in the given image, and disease-associated phenotypic changes can be easily assessed by comparing plant images captured before and after infection. We conducted two case studies involving bacterial and plant mutants with reduced virulence and disease resistance capabilities, respectively, and thereby demonstrated that AraDQ can capture subtle changes in plant color and morphology with a high level of sensitivity. CONCLUSIONS: AraDQ offers a simple, fast, and accurate approach for image-based quantification of plant disease symptoms using various parameters. Its fully automated pipeline neither requires prior image processing nor costly hardware setups, allowing easy implementation of the software by researchers interested in digital phenotyping of diseased plants.
Why it matches plant phenotyping methods植物病徴を画像から定量化するソフトウェアの開発が研究の中心であり、苗の色・形態パラメータを自動抽出して病害症状を評価する。
abstractIn this study, we aimed to develop a digital phenotyping tool to enhance the speed, accuracy, and reliability of disease quantification in Arabidopsis.
Reproduction assets foundThe paper's authors publicly released the AraDQ software package (system code, pretrained deep learning models, installation manual) and the datasets generated and analyzed in the study, including the case-study image files, in their GitHub repository.Code · publicThe portable software, system code, and installation manual are available at https://github.com/kist-smartfarm/AraDQ .Open asset ↗kist-smartfarm/AraDQlines:94-101Dataset · publicThe image files used in this case study are provided in the released dataset on GitHub.Open asset ↗lines:137-212Dataset · publicThe AraDQ software package, including the installation manual, and the datasets generated and analyzed during the current study are available in the GitHub repository at https://github.com/kist-smartfarm/AraDQ .Open asset ↗kist-smartfarm/AraDQlines:137-212Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
MaizeSunflowerField / plotLaboratory / benchtopStem / branchPhysiological trait estimationGrowth / development / phenologyWater status / transpiration
There is currently a need for inexpensive, continuous, non-destructive water potential measurements at high temporal resolution ( Helianthus annuus ) (petioles and stems) and a monocotyledon ( Zea mays ) species (stems) for 1 week during dehydration and re-watering treatments under laboratory conditions. We also demonstrated the ability of the device to record branch and trunk diameter variation of a woody dicotyledon ( Rhus typhina ) in the field. Under laboratory conditions, we compared our device (hereafter 'contact' dendrometer) with modified versions of another open-source dendrometer (the 'optical' dendrometer). Overall, contact and optical dendrometers were well aligned with one another, with Pearson correlation coefficients ranging from 0.77 to 0.97. Both dendrometer devices were well aligned with direct measurements of xylem water potential, with calibration curves exhibiting significant non-linearity, especially at water potentials near the point of incipient plasmolysis, with pseudo R 2 values (Efron) ranging from 0.89 to 0.99. Overall, both dendrometers were comparable and provided sufficient resolution to detect subtle differences in stem water potential (ca. 50 kPa) resulting from light-induced changes in transpiration, vapour pressure deficit and drying/wetting soils. All hardware designs, alternative configurations, software and build instructions for the contact dendrometers are provided.
Why it matches plant phenotyping methods安価なオープンソース樹幹径計を開発し、水ポテンシャルと茎径成長を高時間・空間分解能で測定する手法を比較検証しており、植物表現型取得が研究の中心である。
titleDevelopment and application of an inexpensive open-source dendrometer for detecting xylem water potential and radial stem growth at high spatial and temporal resolution.
Reproduction assets foundThe paper's Data Availability statement explicitly deposits all sensor software, 3D prints, photos, and schematics in a public GitHub repository, and the dendrometer measurement data are provided as a CSV in the supplementary information (no allowed URL for the SI itself). The GitHub repository is a paper-specific,公开,可Code · publicins, CO 80526, USA.
Data Availability
All data used in this study are available for download from the supplemental information as a CSV file (sup_data_all_dendro.csv). All software needed for operating sensors, 3D prints, photos, and schematics have been included in the SI materials, and can also be freely accessed via github ( https://github.com/sean-gl/dendrometer_water_potential_device ).
Sources of Funding
J.J.S. was supported by an NSF Postdoctoral Research Fellowship in Biology, Grant No. IOS-1907338.
Contributions by the Authors
All authors contributed meaningfully to the manuscript. S.M.G., J.J.S., B.A., S.K.P. and J.M. designed the experiment and collected the data. S.M.G. wrote theOpen asset ↗https://github.com/sean-gl/dendrometer_water_potential_devicelines:224-283Code / dataset availability confirmedEurope PMC · checked 7 Sept 2026
Diets consisting of greater quantity/diversity of phytochemicals are correlated with reduced risk of disease. This understanding guides policy development increasing awareness of the importance of consuming fruits, grains, and vegetables. Enacted policies presume uniform concentrations of phytochemicals across crop varieties regardless of production/harvesting methods. A growing body of research suggests that concentrations of phytochemicals can fluctuate within crop varieties. Improved awareness of how cropping practices influence phytochemical concentrations are required, guiding policy development improving human health. Reliable, inexpensive laboratory equipment represents one of several barriers limiting further study of the complex interactions influencing crop phytochemical accumulation. Addressing this limitation our study validated the capacity of a low-cost Reflectometer ($500) to measure phytochemical content in selected crops, against a commercial grade laboratory spectrophotometer. Our correlation results ranged from r 2 = 0.81 for protein in wheat and oats to r 2 = 0.99 for polyphenol content in lettuce in both the Reflectometer and laboratory spectrophotometer assessment, suggesting the Reflectometer provides an accurate accounting of phytochemical content within evaluated crops. Repeatability evaluation demonstrated good reproducibility of the Reflectometer to assess crop phytochemical content. Additionally, we confirmed large variation in phytochemical content within specific crop varieties, suggesting that cultivar is but one of multiple drivers of phytochemical accumulation. Our findings indicate dramatic nutrient variations could exist across the food supply, a point whose implications are not well understood. Future studies should investigate the interactions between crop phytochemical accumulation and farm management practices that influence specific soil characteristics.
Why it matches plant phenotyping methods作物の植物化学成分量を測定する低コスト反射計を、実験室用分光光度計と比較して精度・再現性検証しており、植物形質の取得手法の技術的検証が中心である。
abstractour study validated the capacity of a low-cost Reflectometer ($500) to measure phytochemical content in selected crops, against a commercial grade laboratory spectrophotometer.
Reproduction assets foundThe paper explicitly states that all Bionutrient Institute data (reflectometer/spectrometer phytochemical measurements used in this study) are publicly available in the authors' GitLab repository, and the authors' data-processing pipeline code is also publicly hosted on GitLab.Dataset · publicAll data derived from the Bionutrient Institute methods are available publicly from our repository: https://gitlab.com/our-sci/bionutrient-institute/dataset . The data used in this manuscript covers samples submitted up to 7/31/2022.Open asset ↗our-sci/bionutrient-institute/datasetlines:156-212Code · publicAn automated data pipeline was built using SurveyStacks API’s to merge data from each completed survey and mongoDB scripts ( https://gitlab.com/our-sci/real-food-campaign/lab-data-review-dashboard/-/tree/main ) calculated measurement outcomes.Open asset ↗our-sci/real-food-campaign/lab-data-review-dashboardlines:132-143Code / dataset availability confirmedEurope PMC · checked 7 Sept 2026
Laboratory automation can boost precision and reproducibility of science workflows. However, current laboratory automation systems are difficult to modify for custom applications. Automating new experiment workflows therefore requires development of one-off research platforms, a process which requires significant time, resources, and experience. In this work, we investigate systems to lower the threshold to automation for plant biologists. Our approach establishes a direct connection with a generic motion platform to support experiment development and execution from a computational notebook environment. Specifically, we investigate the use of the open-source tool-changing motion platform Jubilee controlled using Jupyter notebooks. We present the Duckbot, a machine customized for automating laboratory research workflows with duckweed, a common multicellular plant. The Duckbot comprises (1) a set of end-effectors relevant for plant biology, (2) software modules which provide flexible control of these tools, and (3) computational notebooks which make use of these tools to automate duckweed experiments. We demonstrate the Duckbot's functionality by automating a particular laboratory research workflow, namely, duckweed growth assays. The Duckbot supports setting up sample plates with duckweed and growth media, gathering image data, and conducting relevant data analysis. We discuss the opportunities and limitations for developing custom laboratory automation with this platform and provide instructions on usage and customization.
Why it matches plant phenotyping methods植物研究向けの自動化プラットフォームを開発し、画像データ取得と解析を含むduckweed成長アッセイを自動化しており、表現型取得ワークフローが中心的です。
abstractWe present the Duckbot, a machine customized for automating laboratory research workflows with duckweed, a common multicellular plant.
Reproduction assets foundThe authors explicitly state that all design files, build instructions, example data (including the duckweed growth assay images) and analysis scripts are publicly available in their GitHub repositories, which directly reproduce this paper's duckweed phenotyping measurements and computational analysis.Code · publicData Availability: All design files, build instructions, example data and analysis scripts are available at GitHub: https://github.com/machineagency/duckbot and https://github.com/machineagency/science_jubilee/ .Open asset ↗machineagency/duckbotlines:150-163Code · publicData Availability: All design files, build instructions, example data and analysis scripts are available at GitHub: https://github.com/machineagency/duckbot and https://github.com/machineagency/science_jubilee/ .Open asset ↗machineagency/science_jubileelines:150-163Code / dataset availability confirmedCrossref · checked 15 Sept 2026
Quantitative phase imaging by digital holographic microscopy (DHM) is a nondestructive and label-free technique that has been playing an indispensable role in the fields of science, technology, and biomedical imaging. The technique is competent in imaging and analyzing label-free living cells and investigating reflective surfaces. Herein, we introduce a new configuration of a wide field-of-view single-shot common-path off-axis reflective DHM for the quantitative phase imaging of biological cells that leverages several advantages, including being less-vibration sensitive to external perturbations due to its common-path configuration, also being compact in size, simple in optical design, highly stable, and cost-effective. A detailed description of the proposed DHM system, including its optical design, working principle, and capability for phase imaging, is presented. The applications of the proposed system are demonstrated through quantitative phase imaging results obtained from the reflective surface (USAF resolution test target) as well as transparent samples (living plant cells). The proposed system could find its applications in the investigation of several biological specimens and the optical metrology of micro-surfaces.
Why it matches plant phenotyping methods植物細胞を対象に定量位相画像を取得できる新規デジタルホログラフィック顕微鏡を開発しており、植物試料での性能実証も含むため、植物フェノタイピングに利用可能な画像計測法が中心です。
abstractwe introduce a new configuration of a wide field-of-view single-shot common-path off-axis reflective DHM for the quantitative phase imaging of biological cells
Reproduction assets foundThe paper's only paper-specific public asset is the MDPI supplementary material containing the time-lapse retrieved wrapped phase imaging video of tobacco plant cells (the paper's plant-cell phenotyping measurements). No analysis code, datasets, or trained models are publicly deposited; the Data Availability Statement仅Supplement · publicdual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/s24030720/s1 , See the supplementary material for visualization of the time-lapse retrieved wrapped phase imaging video of tobacco plant cells captured five-minute intervals.
Click here for additional data file.
Author Contributions
Conceptualization: M.K.; methodology, M.K.; software, M.K.; validation, M.K., O.M. and T.M.; formal Open asset ↗lines:51-66Code / dataset availability confirmedOpenAlex · Europe PMC · checked 14 Sept 2026
Stalk lodging (structural failure crops prior to harvest) significantly reduces annual yields of vital grain crops. The lack of standardized, high throughput phenotyping methods capable of quantifying biomechanical plant traits prevents comprehensive understanding of the genetic architecture of stalk lodging resistance. A phenotyping pipeline developed to enable higher throughput biomechanical measurements of plant traits related to stalk lodging is presented. The methods were developed using principles from the fields of engineering mechanics and metrology and they enable retention of plant-specific data instead of averaging data across plots as is typical in most phenotyping studies. This pipeline was specifically designed to be implemented in large experimental studies and has been used to phenotype over 40,000 maize stalks. The pipeline includes both lab- and field-based phenotyping methodologies and enables the collection of metadata. Best practices learned by implementing this pipeline over the past three years are presented. The specific instruments (including model numbers and manufacturers) that work well for these methods are presented, however comparable instruments may be used in conjunction with these methods as seen fit.•Efficient methods to measure biomechanical traits and record metadata related to stalk lodging.•Can be used in studies with large sample sizes (i.e., > 1,000).
Why it matches plant phenotyping methodsトウモロコシの倒伏抵抗性に関わる生体力学的形質を高スループットに測定する、実験室・圃場対応の表現型解析パイプラインを開発・実装した研究であり、方法が中心的である。
abstractA phenotyping pipeline developed to enable higher throughput biomechanical measurements of plant traits related to stalk lodging is presented.
Reproduction assets foundThe paper's internode-length phenotyping workflow (YOLOv5m node detection, LabelImg verification, custom R scripts) is publicly available as the authors' InterMeas repository on GitHub, including scripts, example images, and a tutorial. Other assets (Instron methods file, DARLING data) are only supplementary or on-dataCode · publicodal annotations across individual stalks, convert pixel distances to physical distances using the known dimensions of the imaging background, and output internodal lengths as a single excel file of stalk/internode identifiers and lengths. All scripts, example images, and a tutorial on setup and usage are available on Github at https://github.com/nbo245/InterMeas and a Shiny dashboard can be run locally to implement the internode measurement workflow within an interactive GUI environment.
Measurements of minor diameter, rind thickness, rind penetration resistance and integrated puncture scoreOpen asset ↗nbo245/InterMeaslines:85-89Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
Leaf stomata facilitate the exchange of water and CO 2 during photosynthetic gas exchange. The shape, size, and density of leaf pores have not been constant over geologic time, and each morphological trait has potentially been impacted by changing environmental and climatic conditions, especially by changes in the concentration of atmospheric carbon dioxide. As such, stomatal parameters have been used in simple regressions to reconstruct ancient carbon dioxide, as well as incorporated into more complex gas-exchange models that also leverage plant carbon isotope ecology. Most of these proxy relationships are measured on chemically cleared leaves, although newer techniques such as creating stomatal impressions are being increasingly employed. Additionally, many of the proxy relationships use angiosperms with broad leaves, which have been increasingly abundant in the last 130 million years but are absent from the fossil record before this. We focus on the methodology to define stomatal parameters for paleo-CO 2 studies using two separate methodologies (one corrosive, one non-destructive) to prepare leaves on both scale- and broad-leaves collected from herbaria with known global atmospheric CO 2 levels. We find that the corrosive and non-corrosive methodologies give similar values for stomatal density, but that measurements of stomatal sizes, particularly guard cell width (GCW), for the two methodologies are not comparable. Using those measurements to reconstruct CO 2 via the gas exchange model, we found that reconstructed CO 2 based on stomatal impressions (due to inaccurate measurements in GCW) far exceeded measured CO 2 for modern plants. This bias was observed in both coniferous (scale-shaped) and angiosperm (broad) leaves. Thus, we advise that applications of gas exchange models use cleared leaves rather than impressions.
Why it matches plant phenotyping methods葉の気孔形態（密度・サイズ）を測定する2手法を比較・検証し、CO2推定への影響を評価しており、植物表現型取得法が研究の中心です。
abstractWe focus on the methodology to define stomatal parameters for paleo-CO 2 studies using two separate methodologies (one corrosive, one non-destructive) to prepare leaves on both scale- and broad-leaves collected from herbaria with known global atmospheric CO 2 levels.
Reproduction assets foundThe paper's stomatal phenotyping measurements (stomatal density, guard cell length/width, CO2 reconstructions) are publicly deposited as supplemental data tables on Mendeley Data (DOI 10.17632/gs6rn9tjxn.1), explicitly linked in the Supplementary Materials and Data Availability sections. No author analysis code or phenDataset · publicSupplemental Data Tables: All Measurements—Data are available at Mendeley Data: 10.17632/gs6rn9tjxn.1 (accessed on 13 November 2023).Open asset ↗Mendeley Data · 10.17632/gs6rn9tjxn.1lines:58-75Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Laboratory / benchtopSeed / grainVisualization / data managementGrowth / development / phenology
Seed germination is a crucial phase of plant responses in early life to current and future environmental conditions. However, germination data are still scarce or disaggregated for many plant lineages and regions, including global biodiversity hotspots such as the Mediterranean Basin. We present MedGermDB, the first germination database for characteristic species of Mediterranean habitats, as defined by the EUNIS classification. We also present a systematic approach to build germination databases using automatic and semi‐automatic data extraction from the literature. MedGermDB contains germination data for 4680 laboratory tests performed with 236 angiosperm species from 43 families, extracted from 125 literature sources (2837 sources screened). Each test is associated to a seed lot (i.e., a seed collection of a plant species obtained from a specific location at a specific time) and its metadata, recording geographical information and experimental conditions (storage, dormancy‐breaking treatments, incubation temperature, and photoperiod). MedGermDB is available as a csv file, and through a web app: https://dianamariacruztejada.shinyapps.io/medgermdb/. MedGermDB can be used to explore eco‐evolutionary questions and provides a backbone data set for informing effective seed‐based conservation and ecological restoration activities targeting EUNIS habitats. Our methodological approach to data extraction can be extended to other study systems, contributing to global efforts to mobilize germination data.
Why it matches plant phenotyping methods植物の発芽状態に関する大規模データセットを構築し、文献からの自動・半自動データ抽出手法とWebアプリを提示しており、単なる生物学的実験のルーチン測定ではない。
abstractWe present MedGermDB, the first germination database for characteristic species of Mediterranean habitats
Reproduction assets foundThe paper's MedGermDB germination database (supplementary CSVs) and the code/workflow to join database files are publicly available in the authors' GitHub repository, with a Zenodo version of record and a Shiny app for visualization.Code · publicty and Research (MUR) as part of the PON 2014–
2020 “Research and Innovation” resources—Green/Innovation
Action—DM MUR 1061/2022, Number: DOT13GFICX-
2.
CONFLICT OF INTEREST STATEMENT
None.
DATA AVAILABILITY STATEMENT
All data are available as supplementary materials. The data and codes
to join the database files are stored at https://github.com/DianaCruzT
ejada/
MedGe
rmDB and visualized with the shiny app at https://diana
mariacruztejada.shinyapps.io/medgermdb/. A version of record of the
repository can be found at https://
doi.
org/
10.
5281/
zenodo.
10915154.
All people interested in contributing to the growth of this germination
database are encouraged to contact the correspOpen asset ↗MedGermDBpdf-raw-page:6 lines:1-151Code / dataset availability confirmedEurope PMC · OpenAlex · checked 15 Sept 2026
PoplarLaboratory / benchtopRootMorphology / geometry measurement2D/3D reconstructionGrowth / time-series analysisGrowth / development / phenologyRoot system architecture
Root system architecture (RSA) is an important measure of how plants navigate and interact with the soil environment. However, current methods in studying RSA must make tradeoffs between precision of data and proximity to natural conditions, with root growth in germination papers providing accessibility and high data resolution. Functional-structural plant models (FSPMs) can overcome this tradeoff, though parameterization and evaluation of FSPMs are traditionally based in manual measurements and visual comparison. Here, we applied a germination paper system to study the adventitious RSA and root phenology of Populus trichocarpa stem cuttings using time-series image-based phenotyping augmented by FSPM. We found a significant correlation between timing of root initiation and thermal time at cutting collection ( P value = 0.0061, R 2 = 0.875), but little correlation with RSA. We also present a use of RhizoVision [1] for automatically extracting FSPM parameters from time series images and evaluating FSPM simulations. A high accuracy of the parameterization was achieved in predicting 2D growth with a sensitivity rate of 83.5%. This accuracy was lost when predicting 3D growth with sensitivity rates of 38.5% to 48.7%, while overall accuracy varied with phenotyping methods. Despite this loss in accuracy, the new method is amenable to high throughput FSPM parameterization and bridges the gap between advances in time-series phenotyping and FSPMs.
Why it matches plant phenotyping methods時系列画像フェノタイピングとFSPMを統合し、根系形態パラメータを自動抽出・評価する方法が中心である。
abstractwe applied a germination paper system to study the adventitious RSA and root phenology of Populus trichocarpa stem cuttings using time-series image-based phenotyping augmented by FSPM.
Reproduction assets foundThe paper's Data Availability statement deposits all data and R scripts (the paper's phenotyping measurements and analysis) on Zenodo, and the adapted CropRootBox.jl model code on GitHub. Only the Zenodo URL matches an allowed URL, so the Zenodo asset is reported; the GitHub repository is noted but its URL is not in anDataset · publicview and editing: S.P., D.B., K.Y., S.D., and S.-H.K.
Competing interests: The authors declare that there is no conflict of interest regarding the publication of this article.
Data Availability
The model is housed in Github at github.com/uwkimlab/CropRootBox.jl_propagation.jl . All data and and R scripts are housed in Zenodo at https://doi.org/10.5281/zenodo.8083525 .
Supplementary Materials
Supplementary 1
Figs. S1 to S7
Tables S1 to S2
Click here for additional data file.
References
1.
Seethepalli
A , Dhakal
K , Griffiths
M , Guo
H , Freschet
GT , York
LM
.
RhizoVision explorer: Open-source software for root image analysis and measurement standardization
. AoB PLANTS . 2021 ; 13 ( 6 ): pOpen asset ↗Zenodo · 10.5281/zenodo.8083525lines:196-345Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
RiceLaboratory / benchtopRootGrowth / time-series analysisRoot system architecture
The study of plant root growth in real time has been difficult to achieve in an automated, high-throughput, and systematic fashion. Dynamic imaging of plant roots is important in order to discover novel root growth behaviors and to deepen our understanding of how roots interact with their environments. We designed and implemented the Generating Rhizodynamic Observations Over Time (GROOT) robot, an automated, high-throughput imaging system that enables time-lapse imaging of 90 containers of plants and their roots growing in a clear gel medium over the duration of weeks to months. The system uses low-cost, widely available materials. As a proof of concept, we employed GROOT to collect images of root growth of Oryza sativa, Hudsonia montana, and multiple species of orchids including Platanthera integrilabia over six months. Beyond imaging plant roots, our system is highly customizable and can be used to collect time- lapse image data of different container sizes and configurations regardless of what is being imaged, making it applicable to many fields that require longitudinal time-lapse recording.
Why it matches plant phenotyping methods植物根の長期・高スループット画像取得システムを開発し、根成長という植物形質の時系列計測に実証適用しているため、フェノタイピング手法が中心である。
abstractWe designed and implemented the Generating Rhizodynamic Observations Over Time (GROOT) robot, an automated, high-throughput imaging system that enables time-lapse imaging of 90 containers of plants and their roots growing in a clear gel medium over the duration of weeks to months.
Reproduction assets foundThe paper's authors explicitly state that all code files (robot control, QR code generation, image sorting/preprocessing) are publicly available on their GitHub organization, with URLs given in the text. No standalone phenotype dataset deposit is stated, but the authors' analysis/control code qualifies as a paper-sphenCode · publico pmc-prop-manuscript no pmc-prop-legally-suppressed no pmc-prop-has-pdf yes pmc-prop-has-supplement yes pmc-prop-pdf-only no pmc-prop-suppress-copyright no pmc-prop-is-real-version no pmc-prop-is-scanned-article no pmc-prop-preprint no pmc-prop-in-epmc yes pmc-license-ref CC BY Data Availability All code files are available at https://github.com/the-rhizodynamics-robot .
Data Availability
All code files are available at https://github.com/the-rhizodynamics-robot .
Introduction
All organisms must perform effective environmental exploration for survival. Plants are sessile and interact with the location where they grow; therefore, they can only navigate and explore their (typically) below-groOpen asset ↗the-rhizodynamics-robotlines:71-78Code · publicprocessing and analysis of the resulting imaging data. We have included code and documentation for an image preprocessing and time-lapse movie creation system we have developed. This system uses printed QR code labels to identify the individual growth vessels from the raw images ( S3 File : QR Code Generation, code available at https://github.com/orgs/the-rhizodynamics-robot/repositories ), which are then subsequently sorted into individual subdirectories, after which (optionally) stabilized time-lapse videos are created using the open source video editing software FFMPEG [ 24 ] [ S4 File : Image Sorting, code available at https://github.com/the-rhizodynamics-robot ]. This system has been teOpen asset ↗the-rhizodynamics-robotlines:95-102Code / dataset availability confirmedCrossref · checked 14 Sept 2026
Laboratory / benchtopSeed / grainTissueVisualization / data management
Abstract Motivation The propensity of plant tissues to burn (i.e. their flammability) is a key trait to understand fire regimes in many ecosystems across the globe. Measuring plant flammability under laboratory conditions allows us to improve both our understanding of plant evolutionary processes and modelling tools for simulating fire hazard and behaviour. Plant flammability has been studied from different but complementary disciplines (e.g. physics, chemistry, ecology, evolution, forestry). However, information is scattered and standardized terminology is lacking, which slows down the progress of research on plant flammability. Here we provide an open access global database on plant flammability traits measured under laboratory conditions aiming to: (a) identify the diversity of methodologies to measure plant flammability under laboratory conditions; (b) standardize the associated terminology; and (c) find geographical, ecological, and taxonomic gaps in our knowledge on plant flammability. We hope this database will stimulate transdisciplinary research and provide useful information to better cope with an increasingly flammable planet. Main Types of Variables Contained The FLAMITS database contains 19,972 records of 40 flammability variables (classified according to the measured component of flammability). For each record, relevant details of the flammability experiment are given, such as the burning device, the ignition source, and the burnt plant part. In addition, FLAMITS compiles taxonomic and functional data of the studied species and information on the study site (i.e. locality, geographic coordinates, biome, biogeographic realm, and fire activity). Spatial Location and Grain We compiled data from 295 studies in 39 countries and distributed across 12 biomes worldwide. Time Period and Grain The last 62.5 years (1961 to 15th May 2023). Major Taxa and Level of Measurement 1790 plant taxa from 186 families, 883 genera, and 1784 species. Software Format Five text files (.csv), relationally linked.
Why it matches plant phenotyping methods植物の可燃性という観察可能な形質を対象に、測定法の多様性を整理したグローバルデータベースを構築しており、形質取得・方法標準化が中心です。
abstractHere we provide an open access global database on plant flammability traits measured under laboratory conditions aiming to: (a) identify the diversity of methodologies to measure plant flammability under laboratory conditions; (b) standardize the associated terminology
Reproduction assets foundThe paper's core asset is the FLAMITS database itself: five text files (Data, Taxa, Synonymy, Site, Source) containing 19,972 flammability trait records for 1790 taxa. The Data Availability Statement explicitly deposits these files openly in DRYAD (DOI 10.5061/dryad.h18931zr3). The exact Dryad URL is not among the whitDataset · publicDATA AVAILABILITY STATEMENT
The five text files composing the database are openly available in
DRYAD at https://
doi.
org/
10.
5061/
dryad.
h1893
1zr3.Open asset ↗DRYADpdf-raw-page:11 lines:1-102Code / dataset availability confirmedCrossref · checked 14 Sept 2026
Laboratory / benchtopCell / cellular structurePhysiological trait estimationVisualization / data managementGrowth / development / phenology
Abstract Background Plant defense activators offer advantages over pesticides by avoiding the emergence of drug-resistant pathogens. However, only a limited number of compounds have been reported. Reactive oxygen species (ROS) act as not only antimicrobial agents but also signaling molecules that trigger immune responses. They also affect various cellular processes, highlighting the potential ROS modulators as plant defense activators. Establishing a high-throughput screening system for ROS modulators holds great promise for identifying lead chemical compounds with novel modes of action (MoAs). Results We established a novel in silico screening system for plant defense activators using deep learning-based predictions of ROS accumulation combined with the chemical properties of the compounds as explanatory variables. Our screening strategy comprised four phases: (1) development of a ROS inference system based on a deep neural network that combines ROS production data in plant cells and multidimensional chemical features of chemical compounds; (2) in silico extensive-scale screening of seven million commercially available compounds using the ROS inference model; (3) secondary screening by visualization of the chemical space of compounds using the generative topographic mapping; and (4) confirmation and validation of the identified compounds as potential ROS modulators within plant cells. We further characterized the effects of selected chemical compounds on plant cells using molecular biology methods, including pathogenic signal-triggered enzymatic ROS induction and programmed cell death as immune responses. Our results indicate that deep learning-based screening systems can rapidly and effectively identify potential immune signal-inducible ROS modulators with distinct chemical characteristics compared with the actual ROS measurement system in plant cells. Conclusions We developed a model system capable of inferring a diverse range of ROS activity control agents that activate immune responses through the assimilation of chemical features of candidate pesticide compounds. By employing this system in the prescreening phase of actual ROS measurement in plant cells, we anticipate enhanced efficiency and reduced pesticide discovery costs. The in-silico screening methods for identifying plant ROS modulators hold the potential to facilitate the development of diverse plant defense activators with novel MoAs.
Why it matches plant phenotyping methods植物細胞のROS蓄積という生理状態を推定する深層学習モデルと、実測による検証を組み合わせたスクリーニング手法の開発が中心である。
abstractWe established a novel in silico screening system for plant defense activators using deep learning-based predictions of ROS accumulation combined with the chemical properties of the compounds as explanatory variables.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicThe learning algorithm codes used during the current study are available on the GitHub address ( https://github.com/ma1206ko/in_silico_screening ).Open asset ↗ma1206ko/in_silico_screeninglines:168-249Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
The quantification of stomatal pore size has long been a fundamental approach to understand the physiological response of plants in the context of environmental adaptation. Automation of such methodologies not only alleviates human labor and bias but also realizes new experimental research methods through massive analysis. Here, we present an image analysis pipeline that automatically quantifies stomatal aperture of Arabidopsis thaliana leaves from bright-field microscopy images containing mesophyll tissue as noisy backgrounds. By combining a You Only Look Once X-based stomatal detection submodule and a U-Net-based pore segmentation submodule, we achieved a mean average precision with an intersection of union (IoU) threshold of 50% value of 0.875 (stomata detection performance) and an IoU of 0.745 (pore segmentation performance) against images of leaf discs taken with a bright-field microscope. Moreover, we designed a portable imaging device that allows easy acquisition of stomatal images from detached/undetached intact leaves on-site. We demonstrated that this device in combination with fine-tuned models of the pipeline we generated here provides robust measurements that can substitute for manual measurement of stomatal responses against pathogen inoculation. Utilization of our hardware and pipeline for automated stomatal aperture measurements is expected to accelerate research on stomatal biology of model dicots.
Why it matches plant phenotyping methods葉画像から気孔開度を自動抽出する画像解析パイプラインと携帯型撮像装置を開発・性能評価しており、植物表現型取得が中心である。
abstractwe present an image analysis pipeline that automatically quantifies stomatal aperture of Arabidopsis thaliana leaves
Reproduction assets foundThe paper's Data Availability section explicitly deposits the authors' ONNX model weights and pipeline code, plus masked/unmasked test images, on a public GitHub repository and Zenodo (DOI 10.5281/zenodo.7549843). These are paper-specific, publicly actionable assets for the stomatal aperture phenotyping pipeline. The YCode · publicPlant Cell Physiol. 00(00): 1–10 (2023) doi:https://doi.org/10.1093/pcp/pcad018
Supplementary Data
Supplementary data are available at PCP online.
Data Availability
The model weights and codes in ONNX format to execute
the Arabidopsis stomata quantification pipeline and mask
and unmasked test data are available at https://github.com/phytometrics/arabidopsis_leaf_stomata_quantification.Model weights and the test images are also available on Zen-
odo with the following DOI: https://doi.org/10.5281/zenodo.7549843. The software used to process image streams from the
portable device is under development at https://github.com/phytometrics/cvgui_linux.Funding
Grant-in-Aid for Transformative ResearcOpen asset ↗phytometrics/arabidopsis_leaf_stomata_quantificationpdf-raw-page:9 lines:1-84Dataset · publicData Availability
The model weights and codes in ONNX format to execute
the Arabidopsis stomata quantification pipeline and mask
and unmasked test data are available at https://github.com/phytometrics/arabidopsis_leaf_stomata_quantification.Model weights and the test images are also available on Zen-
odo with the following DOI: https://doi.org/10.5281/zenodo.7549843. The software used to process image streams from the
portable device is under development at https://github.com/phytometrics/cvgui_linux.Funding
Grant-in-Aid for Transformative Research Areas (21H05151 and
21H05149 to A.M. and 21H05152 to Y.T.), Grant-in-Aid for Sci-
entific Research (B) (19H02960 to A. M.), and Grant-in-Aid foOpen asset ↗10.5281/zenodo.7549843pdf-raw-page:9 lines:1-84Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
One of the fundamental questions in plant developmental biology is how cell proliferation and cell expansion coordinately determine organ growth and morphology. An amenable system to address this question is the Arabidopsis root tip, where cell proliferation and elongation occur in spatially separated domains, and cell morphologies can easily be observed using a confocal microscope. While past studies revealed numerous elements of root growth regulation including gene regulatory networks, hormone transport and signaling, cell mechanics and environmental perception, how cells divide and elongate under possible constraints from cell lineages and neighboring cell files has not been analyzed quantitatively. This is mainly due to the technical difficulties in capturing cell division and elongation dynamics at the tip of growing roots, as well as an extremely labor-intensive task of tracing the lineages of frequently dividing cells. Here, we developed a motion-tracking confocal microscope and an Artificial Intelligence (AI)-assisted image-processing pipeline that enables semi-automated quantification of cell division and elongation dynamics at the tip of vertically growing Arabidopsis roots. We also implemented a data sonification tool that facilitates human recognition of cell division synchrony. Using these tools, we revealed previously unnoted lineage-constrained dynamics of cell division and elongation, and their contribution to the root zonation boundaries.
Why it matches plant phenotyping methods生長中のシロイヌナズナ根端における細胞分裂・伸長という植物形態動態を、4D顕微鏡、AI画像処理、追跡、データソニフィケーションで半自動定量する手法を開発しており、フェノタイピング手法が中心である。
abstractHere, we developed a motion-tracking confocal microscope and an Artificial Intelligence (AI)-assisted image-processing pipeline that enables semi-automated quantification of cell division and elongation dynamics at the tip of vertically growing Arabidopsis roots.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicThe codes for the nuclei detection and cell tracking are available on the GitHub ( https://github.com/JerrySongCST/Arabidopsis_root_cortex_cell_tracking ).Open asset ↗JerrySongCST/Arabidopsis_root_cortex_cell_trackinglines:152-227Code / dataset availability confirmedOpenAlex · Europe PMC · bioRxiv · checked 7 Sept 2026
Abstract Image segmentation is commonly used to estimate the location and shape of plants and their external structures. Segmentation masks are then used to localize landmarks of interest and compute other geometric features that correspond to the plant’s phenotype. Despite its prevalence, segmentation-based approaches are laborious (requiring extensive annotation to train), and error-prone (derived geometric features are sensitive to instance mask integrity). Here we present a segmentation-free approach which leverages deep learning-based landmark detection and grouping, also known as pose estimation. We use a tool originally developed for animal motion capture called SLEAP (Social LEAP Estimates Animal Poses) to automate the detection of distinct morphological landmarks on plant roots. Using a gel cylinder imaging system across multiple species, we show that our approach can reliably and efficiently recover root system topology at high accuracy, few annotated samples, and faster speed than segmentation-based approaches. In order to make use of this landmark-based representation for root phenotyping, we developed a Python library ( sleap-roots ) for trait extraction directly comparable to existing segmentation-based analysis software. We show that landmark-derived root traits are highly accurate and can be used for common downstream tasks including genotype classification and unsupervised trait mapping. Altogether, this work establishes the validity and advantages of pose estimation-based plant phenotyping. To facilitate adoption of this easy-to-use tool and to encourage further development, we make sleap-roots , all training data, models, and trait extraction code available at: https://github.com/talmolab/sleap-roots and https://osf.io/k7j9g/ .
Why it matches plant phenotyping methods植物根の形態ランドマークをポーズ推定で検出し、根系形質を抽出する手法とソフトウェアを開発・検証した研究であり、植物フェノタイピング手法が中心である。
abstractHere we present a segmentation-free approach which leverages deep learning-based landmark detection and grouping, also known as pose estimation.
Reproduction assets foundThe paper makes its root phenotyping assets public: labeled training data, trained SLEAP models, and analysis files on OSF, the sleap-roots trait-extraction codebase on GitHub, and a separate figure-replication code repository.Dataset · publicThe datasets generated and/or analyzed during the current study are available in the Open Science Framework (OSF) repository. This includes the labeled data, predictive models, and analysis files which can be accessed via the following link: https://osf.io/k7j9g/ .Open asset ↗osf.io/k7j9glines:752-811Code · publicAdditionally, the specific code utilized for replicating the figures presented in this study can be found in a separate GitHub repository here: https://github.com/talmolab/Berrigan_et_al_sleap-roots .Open asset ↗talmolab/Berrigan_et_al_sleap-rootslines:752-811Code / dataset availability confirmedEurope PMC · checked 7 Sept 2026
ArabidopsisLaboratory / benchtopRGB / grayscaleRootTrackingRoot system architecture
Plant roots elongate when cells produced in the apical meristem enter a transient period of rapid expansion. To measure the dynamic process of root cell expansion in the elongation zone, we captured digital images of growing Arabidopsis roots with horizontal microscopes and analyzed them with a custom image analysis program (PatchTrack) designed to track the growth-driven displacement of many closely spaced image patches. Fitting a flexible logistics equation to patch velocities plotted versus position along the root axis produced the length of the elongation zone (mm), peak relative elemental growth rate (% h -1 ), the axial position of the peak (mm from the tip), and average root elongation rate (mm h -1 ). For a wild-type root, the average values of these kinematic traits were 0.52 mm, 23.7% h -1 , 0.35 mm, and 0.1 mm h -1 , respectively. We used the platform to determine the kinematic phenotypes of auxin transport mutants. The results support a model in which the PIN2 auxin transporter creates an area of expansion-suppressing, supraoptimal auxin concentration that ends 0.1 mm from the quiescent center (QC), and that ABCB4 and ABCB19 auxin transporters maintain expansion-limiting suboptimal auxin levels beginning approximately 0.5 mm from the QC. This study shows that PatchTrack can quantify dynamic root phenotypes in kinematic terms.
Why it matches plant phenotyping methodsPatchTrackによる画像解析で根の動的な伸長・細胞伸長形質を抽出する手法とプラットフォームを開発・実証しており、表現型取得が研究の中心です。
abstractanalyzed them with a custom image analysis program (PatchTrack) designed to track the growth-driven displacement of many closely spaced image patches.
Reproduction assets foundThe paper's Data Availability Statement explicitly deposits the authors' PatchTrack image-analysis code (used to produce the kinematic phenotyping measurements) on a public GitHub repository. No phenotype dataset or image deposit is stated.Code · publicThe computer code for PatchTrack is available at https://github.com/phytoMorph/phytoMorph_kinematics .Open asset ↗phytoMorph/phytoMorph_kinematicslines:96-111Code / dataset availability confirmedOpenAlex · Crossref · Europe PMC · checked 15 Sept 2026
BACKGROUND: Object detection, size determination, and colour detection of images are tools commonly used in plant science. Key examples of this include identification of ripening stages of fruit such as tomatoes and the determination of chlorophyll content as an indicator of plant health. While methods exist for determining these important phenotypes, they often require proprietary software or require coding knowledge to adapt existing code. RESULTS: We provide a set of free and open-source Python scripts that, without any adaptation, are able to perform background correction and colour correction on images using a ColourChecker chart. Further scripts identify objects, use an object of known size to calibrate for size, and extract the average colour of objects in RGB, Lab, and YUV colour spaces. We use two examples to demonstrate the use of these scripts. We show the consistency of these scripts by imaging in four different lighting conditions, and then we use two examples to show how the scripts can be used. In the first example, we estimate the lycopene content in tomatoes (Solanum lycopersicum) var. Tiny Tim using fruit images and an exponential model to predict lycopene content. We demonstrate that three different cameras (a DSLR camera and two separate mobile phones) are all able to model lycopene content. The models that predict lycopene or chlorophyll need to be adjusted depending on the camera used. In the second example, we estimate the chlorophyll content of basil (Ocimum basilicum) using leaf images and an exponential model to predict chlorophyll content. CONCLUSION: A fast, cheap, non-destructive, and inexpensive method is provided for the determination of the size and colour of plant materials using a rig consisting of a lightbox, camera, and colour checker card and using free and open-source scripts that run in Python 3.8. This method accurately predicted the lycopene content in tomato fruit and the chlorophyll content in basil leaves.
Why it matches plant phenotyping methods植物画像からサイズ・色を抽出し、果実リコピンや葉クロロフィルを推定するオープンソース手法と撮像系を開発・検証しており、表現型取得が研究の中心である。
abstractWe provide a set of free and open-source Python scripts that, without any adaptation, are able to perform background correction and colour correction on images using a ColourChecker chart.
Reproduction assets foundThe authors provide public, paper-specific assets: the PlantSizeClr Python scripts on GitHub, a snapshot of all scripts and data on OSF, and all data generated for the manuscript on the University of Sheffield data repository.Code · publicThe example lightbox contains LED lighting; this could be further improved by using bulbs that are closer to standard illuminants (D65 for sRGB).
An object of known size (coins work well).
Software: Python 3.8.
Python packages: List of packages and their versions used available in Additional file 1 : S0.
Custom Python Scripts: https://github.com/HarryCWright/PlantSizeClr
Snapshot of all scripts and data is available on Open Science Framework: www.doi.org/10.17605/OSF.IO/QAYMU
Optional for extraction of lycopene: acetone, high purity ethanol, hexane deionised water and a UV/vis spectrophotometerOpen asset ↗HarryCWright/PlantSizeClrlines:34-50Code · publicSnapshot of all scripts and data is available on Open Science Framework: www.doi.org/10.17605/OSF.IO/QAYMUOpen asset ↗OSF.IO/QAYMU · 10.17605/OSF.IO/QAYMUlines:34-50Code / dataset availability confirmedEurope PMC · checked 7 Sept 2026
In vitro pollen germination is considered the most efficient method to assess pollen viability. The pollen germination frequency and pollen tube length, which are key indicators of pollen viability, should be accurately measured during in vitro culture. In this study, a Mask R-CNN model trained using microscopic images of tree peony (Paeonia suffruticosa) pollen has been proposed to rapidly detect the pollen germination rate and pollen tube length. To reduce the workload during image acquisition, images of synthesized crossed pollen tubes were added to the training dataset, significantly improving the model accuracy in recognizing crossed pollen tubes. At an Intersection over Union threshold of 50%, a mean average precision of 0.949 was achieved. The performance of the model was verified using 120 testing images. The R2 value of the linear regression model using detected pollen germination frequency against the ground truth was 0.909 and that using average pollen tube length was 0.958. Further, the model was successfully applied to two other plant species, indicating a good generalizability and potential to be applied widely.
Why it matches plant phenotyping methods顕微鏡画像から花粉発芽率と花粉管長を自動推定するMask R-CNN手法を開発し、精度検証と他種への適用を行っており、植物表現型取得が研究の中心です。
abstracta Mask R-CNN model trained using microscopic images of tree peony (Paeonia suffruticosa) pollen has been proposed to rapidly detect the pollen germination rate and pollen tube length.
Reproduction assets foundThe paper's Data availability statement explicitly deposits the authors' Mask R-CNN pollen germination detection code in a public GitHub repository. Training/testing images are only available upon request (request_only), but the code asset qualifies as public and paper-specific. The makesense.ai URL is a generic third‑Code · publicThe code for local execution of the proposed model can be found in the GitHub repository ( https://github.com/Nihon-snail/Pollen_germination_detection ). Other data such as training and testing images can be provided upon reasonable request.Open asset ↗Nihon-snail/Pollen_germination_detectionlines:109-144Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Computer vision is a powerful technology that has enabled solutions in various fields by analyzing visual attributes in images. One field that has taken advantage of computer vision is agricultural automation, which promotes high-quality crop production. The nutritional status of a crop is a crucial factor in determining its productivity. This status is mediated by approximately 14 chemical elements acquired by the plant, and their determination plays a pivotal role in farm management. To address the timely identification of nutritional disorders, this study focuses on the classification of three levels of phosphorus deficiencies through individual leaf analysis. The methodological steps include: (1) generating a database with laboratory-grown maize plants that were induced to total phosphorus deficiency, medium deficiency, and total nutrition, using different capture devices; (2) processing the images with state-of-the-art transfer learning architectures (i.e. VGG16, ResNet50, GoogLeNet, DenseNet201, and MobileNetV2); and (3) evaluating the classification performance of the models using the created database. The results show that the VGG16 model achieves superior performance, with 98% classification accuracy. However, the other studied architectures also demonstrate competitive performance and are considered state-of-the-art automatic leaf deficiency detection tools. The proposed method can be a starting point to fine-tune machine vision-based solutions tailored for real-time monitoring of crop nutritional status.
Why it matches plant phenotyping methodsトウモロコシ葉画像からリン欠乏状態を分類する画像解析手法を構築・評価しており、植物の栄養状態という表現型の取得が研究の中心である。
abstractthis study focuses on the classification of three levels of phosphorus deficiencies through individual leaf analysis.
Reproduction assets foundThe authors explicitly state that the complete generated maize-leaf phosphorus-deficiency image dataset (2,433 labeled images across three nutrition classes) is freely available on Zenodo, a paper-specific public asset directly reproducing this paper's phenotyping measurements.Dataset · publicwriting – original draft, M.R.; writing – review & editing, A.M., C.T.
and L.G. All authors have read and agreed to the published version of the manuscript.
Funding: This research was funded by Universidad EAFIT.
Data Availability Statement: The complete generated dataset presented in this work is freely available at Zenodo,
at https://zenodo.org/records/10041514.
Acknowledgments: M. Ramos-Ospina and A. Marulanda-Tobón acknowledge the support from María Isabel
Hernández-Pérez, head of the Undergraduate Program in Agricultural Engineering, from School of Applied
Sciences and Engineering, Universidad EAFIT, for the scientific assistance provided during the realization of this
work.
ConfliOpen asset ↗Zenodo · 10041514pdf-layout-page:23 lines:1-68Code / dataset availability confirmedEurope PMC · OpenAlex · Crossref · checked 7 Sept 2026
MaizeLaboratory / benchtopStereoRootMorphology / geometry measurement2D/3D reconstructionGrowth / time-series analysisGrowth / development / phenologyRoot system architecture
Background: The root of a plant is a fundamental organ for the multisensory perception of the environment. Investigating root growth dynamics as a mean of their interaction with the environment is of key importance for improving knowledge in plant behaviour, plant biology and agriculture. To date, it is difficult to study roots movements from a dynamic perspective given that available technologies for root imaging focus mostly on static characterizations, lacking of temporal and three-dimensional (3D) spatial information. This paper describes a new system based on timelapse for the 3D reconstruction and analysis of roots growing in hydroponics. Results The system is based on infrared stereo-cameras acquiring time-lapse images of the roots for 3D reconstruction. The acquisition protocol guarantees the root growth in complete dark while the upper part of the plant grows in normal light conditions. The system extracts the 3D trajectory of the root tip and a set of descriptive features in both the temporal and frequency domains. The system has been used on Zea mays L. (B73) during the first week of growth and shows good inter-reliability between operators with an Intra Class Correlation Coefficient (ICC) > 0.9 for all features extracted. It also showed measurement accuracy with a median difference of < 1 mm between computed and manually measured root length. Conclusions The system and the protocol presented in this study enable accurate 3D analysis of primary root growth in hydroponics. It can serve as a valuable tool for analyzing real-time root responses to environmental stimuli thus improving knowledge on the processes contributing to roots physiological and phenotypic plasticity.
Why it matches plant phenotyping methods根の3D動態を画像から再構成・解析するシステムを開発し、特徴量の信頼性と測定精度を検証しており、植物表現型取得法が中心である。
abstractThis paper describes a new system based on timelapse for the 3D reconstruction and analysis of roots growing in hydroponics.
Reproduction assets foundThe preprint explicitly states that the 3D root tip trajectory data underlying its phenotyping analysis are publicly deposited on Zenodo (record 8422242), making this a paper-specific, publicly accessible phenotype dataset. No author analysis code with a public URL is stated (SPROUTS is proprietary third-party softwareDataset · publicData describing 3D trajectories used in this paper are available here: https://zenodo.org/record/8422242Open asset ↗Zenodo · 8422242lines:119-156Code / dataset availability confirmedEurope PMC · checked 7 Sept 2026
Duckweeds, a family of floating aquatic plants, are ideal model plants for laboratory experiments because they are small, easy to cultivate, and reproduce quickly. Duckweed cultivation, for the purposes of scientific research, requires that lineages are maintained as continuous populations of asexually propagating fronds, so research teams need to develop optimized cultivation conditions and coordinate maintenance tasks for duckweed stocks. Additionally, computational image analysis is proving to be a powerful duckweed research tool, but researchers lack software tools to assist with data collection and storage in a way that can feed into scripted data analysis. We set out to support these processes using a laboratory management software called Aquarium, an open-source application developed to manage laboratory inventory and plan experiments. We developed a suite of duckweed cultivation and experimentation operation types in Aquarium, which we then integrated with novel data analysis scripts. We then demonstrated the efficacy of our system with a series of image-based growth assays, and explored how our framework could be used to develop optimized cultivation protocols. We discuss the unexpected advantages and the limitations of this approach, suggesting areas for future software tool development. In its current state, our approach helps to bridge the gap between laboratory implementation and data analytical software for duckweed biologists and builds a foundation for future development of end-to-end computational tools in plant science.
Why it matches plant phenotyping methodsアヒルウキクサの画像ベース成長アッセイを含む、培養・実験管理ソフトウェアとデータ解析ワークフローの開発が中心であり、植物表現型取得を支援する方法論的貢献である。
abstractcomputational image analysis is proving to be a powerful duckweed research tool, but researchers lack software tools to assist with data collection and storage in a way that can feed into scripted data analysis.
Reproduction assets foundThe paper's duckweed growth-assay experimental data and Python analysis scripts are publicly available in the authors' GitHub repository, explicitly stated in the availability statement and results sections. The Aquarium platform itself is a generic pre-existing tool, not a paper-specific asset.Code · publicAll code used in this study is available on Github.Open asset ↗lines:119-135Dataset · publicThe datasets generated and/or analyzed during the current study are available in the Github repository, https://github.com/mtscott321/duckweed_data_analysis .Open asset ↗mtscott321/duckweed_data_analysislines:119-135Code / dataset availability confirmedOpenAlex · Europe PMC · Crossref · checked 14 Sept 2026
Premise: Higher temperatures across the globe are causing an increase in the frequency and severity of droughts. In agricultural crops, this results in reduced yields, financial losses, and increased food costs at the supermarket. Root growth maintenance in drying soils plays a major role in a plant's ability to survive and perform under drought, but phenotyping root growth is extremely difficult due to roots being under the soil. Methods and Results: RootBot is an automated high-throughput phenotyping robot that eliminates many of the difficulties and reduces the time required for performing drought-stress studies on primary roots. RootBot simulates root growth conditions using transparent plates to create a gap that is filled with soil and polyethylene glycol (PEG) to simulate low soil moisture. RootBot has a gantry system with vertical slots to hold the transparent plates, which theoretically allows for evaluating more than 50 plates at a time. Software pipelines were also co-opted, developed, tested, and extensively refined for running the RootBot imaging process, storing and organizing the images, and analyzing and extracting data. Conclusions: The RootBot platform and the lessons learned from its design and testing represent a valuable resource for better understanding drought tolerance mechanisms in roots, as well as for identifying breeding and genetic engineering targets for crop plants.
Why it matches plant phenotyping methods根の乾燥ストレス下での成長を自動撮像・解析する高スループット表現型解析ロボットの開発、試験、画像データ抽出が中心である。
abstractRootBot is an automated high-throughput phenotyping robot that eliminates many of the difficulties and reduces the time required for performing drought-stress studies on primary roots.
Reproduction assets foundThe paper's authors publicly released all RootBot source code, scripts, and CAD files on BitBucket, plus step-by-step protocols on protocols.io for the RootBot/FarmBot OS phenotype scheduling and the image scoring/analysis pipeline used to extract root measurements. No raw phenotype dataset deposit is stated beyond theCode · publicThomas S. K., Guill K. E., et al. 2023. RootBot: High‐throughput root stress phenotyping robot. Applications in Plant Sciences
11(6): e11541. 10.1002/aps3.11541
Mia Ruppel and Sven K. Nelson contributed equally to this work.
DATA AVAILABILITY STATEMENT
All source code, scripts, and CAD files are freely available on BitBucket ( https://bitbucket.org/washjake/rootbot/ ). The RootBot/FarmBot OS setup, programming, and phenotype scheduling ( https://doi.org/10.17504/protocols.io.x54v9d76zg3e/v1 ) and the image scoring protocol ( https://doi.org/10.17504/protocols.io.5jyl8j16dg2w/v1 ) are available on protocols.io (Ruppel et al., 2023a , b ).
REFERENCES
Daryanto, S.
, Wang L., and Jacinthe P.‐AOpen asset ↗bitbucket.org/washjake/rootbotlines:132-394Code · publicPlant Sciences
11(6): e11541. 10.1002/aps3.11541
Mia Ruppel and Sven K. Nelson contributed equally to this work.
DATA AVAILABILITY STATEMENT
All source code, scripts, and CAD files are freely available on BitBucket ( https://bitbucket.org/washjake/rootbot/ ). The RootBot/FarmBot OS setup, programming, and phenotype scheduling ( https://doi.org/10.17504/protocols.io.x54v9d76zg3e/v1 ) and the image scoring protocol ( https://doi.org/10.17504/protocols.io.5jyl8j16dg2w/v1 ) are available on protocols.io (Ruppel et al., 2023a , b ).
REFERENCES
Daryanto, S.
, Wang L., and Jacinthe P.‐A.. 2016. Global synthesis of drought effects on maize and wheat production. PLoS ONE
11: e0156362.
Das, A.
, SchneOpen asset ↗10.17504/protocols.io.x54v9d76zg3e/v1lines:132-394Code · publicd equally to this work.
DATA AVAILABILITY STATEMENT
All source code, scripts, and CAD files are freely available on BitBucket ( https://bitbucket.org/washjake/rootbot/ ). The RootBot/FarmBot OS setup, programming, and phenotype scheduling ( https://doi.org/10.17504/protocols.io.x54v9d76zg3e/v1 ) and the image scoring protocol ( https://doi.org/10.17504/protocols.io.5jyl8j16dg2w/v1 ) are available on protocols.io (Ruppel et al., 2023a , b ).
REFERENCES
Daryanto, S.
, Wang L., and Jacinthe P.‐A.. 2016. Global synthesis of drought effects on maize and wheat production. PLoS ONE
11: e0156362.
Das, A.
, Schneider H., Burridge J., Ascanio A. K. M., Wojciechowski T., Topp C. N., Lynch J. P., et al.Open asset ↗10.17504/protocols.io.5jyl8j16dg2w/v1lines:132-394Code / dataset availability confirmedEurope PMC · Crossref · checked 7 Sept 2026
Background Rust is a damaging disease affecting vital crops, including pea, and identifying highly resistant genotypes remains a challenge. Accurate measurement of infection levels in large germplasm collections is crucial for finding new resistance sources. Current evaluation methods rely on visual estimation of disease severity and infection type under field or controlled conditions. While they identify some resistance sources, they are error-prone and time-consuming. An image analysis system proves useful, providing an easy-to-use and affordable way to quickly count and measure rust-induced pustules on pea samples. This study aimed to develop an automated image analysis pipeline for accurately calculating rust disease progression parameters under controlled conditions, ensuring reliable data collection. Results A highly efficient and automatic image-based method for assessing rust disease in pea leaves was developed using R. The method's optimization and validation involved testing different segmentation indices and image resolutions on 600 pea leaflets with rust symptoms. The approach allows automatic estimation of parameters like pustule number, pustule size, leaf area, and percentage of pustule coverage. It reconstructs time series data for each leaf and integrates daily estimates into disease progression parameters, including latency period and area under the disease progression curve. Significant variation in disease responses was observed between genotypes using both visual ratings and image-based analysis. Among assessed segmentation indices, the Normalized Green Red Difference Index (NGRDI) proved fastest, analysing 600 leaflets at 60% resolution in 62 s with parallel processing. Lin's concordance correlation coefficient between image-based and visual pustule counting showed over 0.98 accuracy at full resolution. While lower resolution slightly reduced accuracy, differences were statistically insignificant for most disease progression parameters, significantly reducing processing time and storage space. NGRDI was optimal at all time points, providing highly accurate estimations with minimal accumulated error. Conclusions A new image-based method for monitoring pea rust disease in detached leaves, using RGB spectral indices segmentation and pixel value thresholding, improves resolution and precision. It rapidly analyses hundreds of images with accuracy comparable to visual methods and higher than other image-based approaches. This method evaluates rust progression in pea, eliminating rater-induced errors from traditional methods. Implementing this approach to evaluate large germplasm collections will improve our understanding of plant-pathogen interactions and aid future breeding for novel pea cultivars with increased rust resistance.
Why it matches plant phenotyping methodsエンドツーエンドのRGB画像解析パイプラインを開発・最適化・検証し、エンドウ葉のさび病症状と病勢進展を定量化する方法が研究の中心である。
abstractThis study aimed to develop an automated image analysis pipeline for accurately calculating rust disease progression parameters under controlled conditions, ensuring reliable data collection.
Reproduction assets foundThe authors deposited the R analysis script and the 600 pea leaflet images used in this rust phenotyping study in a public Zenodo repository, explicitly cited in the Data Availability statement and reference list.Dataset · publicThe datasets generated during and/or analysed during the current study are available in the Zenodo repository, https://doi.org/10.5281/zenodo.7991462 [ 93 ].Open asset ↗Zenodo · 10.5281/zenodo.7991462lines:147-229Code / dataset availability confirmedOpenAlex · checked 14 Sept 2026
Abstract Aims Our understanding of the rhizosphere is limited by the lack of techniques for in situ live microscopy. Current techniques are either destructive or unsuitable for observing chemical changes within the pore space. To address this limitation, we have developed artificial substrates, termed smart soils, that enable the acquisition and 3D reconstruction of chemical sensors attached to soil particles. Methods The transparency of smart soils was achieved using polymer particles with refractive index matching that of water. The surface of the particles was modified both to retain water and act as a local sensor to report on pore space pH via fluorescence emissions. Multispectral signals were acquired from the particles using a light sheet microscope, and machine learning algorithms predicted the changes and spatial distribution in pH at the surface of the smart soil particles. Results The technique was able to predict pH live and in situ within ± 0.5 units of the true pH value. pH distribution could be reconstructed across a volume of several cubic centimetres around plant roots at 10 μm resolution. Using smart soils of different composition, we revealed how root exudation and pore structure create variability in chemical properties. Conclusion Smart soils captured the pH gradients forming around a growing plant root. Future developments of the technology could include the fine tuning of soil physicochemical properties, the addition of chemical sensors and improved data processing. Hence, this technology could play a critical role in advancing our understanding of complex rhizosphere processes.
Why it matches plant phenotyping methods植物根圏のpHを生体根周辺で測定・3D再構成するセンサー基盤を開発し、精度検証まで行っており、植物状態の取得方法が研究の中心である。
abstractwe have developed artificial substrates, termed smart soils, that enable the acquisition and 3D reconstruction of chemical sensors attached to soil particles.
Reproduction assets foundThe paper's Data availability statement explicitly releases the authors' software for predicting pH from light-sheet image data (the machine-learning phenotyping analysis) on the authors' public GitHub repository SENSOIL. No separate phenotype/trait dataset or image deposit is stated; supplementary material is only a 'Code · public102 Plant Soil (2024) 500:91–104
1 3
Vol:. (1234567890)
Data availability Software developped for predicting pH
from image data is available at https://github.com/LionelDu-puy/SENSOIL/tree/main/pH_Release.Declarations
Competing interest There is no competing interest.
Open Access This article is licensed under a Creative
Commons Attribution 4.0 International License, which per-
mits use, sharing, adaptation, distribution and reproduction in
any medium or format, as long as you give appropriate credit
to the original author(s) and the source,Open asset ↗SENSOILpdf-raw-page:12 lines:1-92Code / dataset availability confirmedOpenAlex · Europe PMC · Crossref · checked 7 Sept 2026
Studying the complex web of interactions in biological communities requires large multifactorial experiments with sufficient statistical power. Automation tools reduce the time and labor associated with setup, data collection, and analysis in experiments that untangle these webs. We developed tools for high-throughput experimentation (HTE) in duckweeds, small aquatic plants that are amenable to autonomous experimental preparation and image-based phenotyping. We showcase the abilities of our HTE system in a study with 6,000 experimental units grown across 2,000 treatments. These automated tools facilitated the collection and analysis of time-resolved growth data, which revealed finer dynamics of plant-microbe interactions across environmental gradients. Altogether, our HTE system can run experiments with up to 11,520 experimental units and can be adapted for other small organisms.
Why it matches plant phenotyping methodsアヒルウキクサを対象に、自動化された大規模実験系と画像ベースの時系列成長データ取得・解析を開発・提示しており、植物フェノタイピング基盤が研究の中心である。
abstractWe developed tools for high-throughput experimentation (HTE) in duckweeds, small aquatic plants that are amenable to autonomous experimental preparation and image-based phenotyping.
Reproduction assets foundThe paper's Data Availability statement explicitly deposits the authors' data (Dryad) and code (Zenodo) for this duckweed high-throughput imaging/phenotyping study.Dataset · publicData Availability: We have made our data and code available at the following repositories: Dryad: https://doi.org/10.5061/dryad.t4b8gtj6tOpen asset ↗Dryad · 10.5061/dryad.t4b8gtj6tlines:170-179Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
In vivo microscopy of plants with high-frequency imaging allows observation and characterization of the dynamic responses of plants to stimuli. It provides access to responses that could not be observed by imaging at a given time point. Such methods are particularly suitable for the observation of fast cellular events such as membrane potential changes. Classical measurement of membrane potential by probe impaling gives quantitative and precise measurements. However, it is invasive, requires specialized equipment, and only allows measurement of one cell at a time. To circumvent some of these limitations, we developed a method to relatively quantify membrane potential variations in Arabidopsis thaliana roots using the fluorescence of the voltage reporter DISBAC 2 (3). In this protocol, we describe how to prepare experiments for agar media and microfluidics, and we detail the image analysis. We take an example of the rapid plasma membrane depolarization induced by the phytohormone auxin to illustrate the method. Relative membrane potential measurements using DISBAC 2 (3) fluorescence increase the spatio-temporal resolution of the measurements and are non-invasive and suitable for live imaging of growing roots. Studying membrane potential with a more flexible method allows to efficiently combine mature electrophysiology literature and new molecular knowledge to achieve a better understanding of plant behaviors. Key features Non-invasive method to relatively quantify membrane potential in plant roots. Method suitable for imaging seedlings root in agar or liquid medium. Straightforward quantification.
Why it matches plant phenotyping methods植物根の膜電位を蛍光画像から定量する非侵襲的手法の開発と画像解析プロトコルが中心であり、植物表現型計測法に該当する。
abstractwe developed a method to relatively quantify membrane potential variations in Arabidopsis thaliana roots using the fluorescence of the voltage reporter DISBAC 2 (3).
Reproduction assets foundThe protocol explicitly states that the raw imaging data re-analyzed in the paper are deposited on Zenodo and that all analysis scripts (R and Python) are available in a public SourceForge repository. Both are paper-specific, public, and actionable.Dataset · publicluorescence only in the root transition zone. Moreover, we focus on the interface between the cortex and the epidermis, as the dead lateral root cap cells were strongly fluorescent (open membranes for the dye to react to). The data presented here are re-analyzed images from Serre et al. (2021). Raw data can be found on Zenodo ( https://zenodo.org/record/4922659 ). All the scripts used in this protocol can be found on the public repository https://sourceforge.net/projects/disbac2-3-data-analysis/ .
Here, we describe a method to:
Quantify DISBAC 2 (3) fluorescence in the transition zone at a given point (agar experiment) or over time (microfluidics) using the ImageJ/Fiji software.
QuantOpen asset ↗Zenodo · 4922659lines:168-214Code · publicermis, as the dead lateral root cap cells were strongly fluorescent (open membranes for the dye to react to). The data presented here are re-analyzed images from Serre et al. (2021). Raw data can be found on Zenodo ( https://zenodo.org/record/4922659 ). All the scripts used in this protocol can be found on the public repository https://sourceforge.net/projects/disbac2-3-data-analysis/ .
Here, we describe a method to:
Quantify DISBAC 2 (3) fluorescence in the transition zone at a given point (agar experiment) or over time (microfluidics) using the ImageJ/Fiji software.
Quantify root elongation either as an average growth (agar experiment) or over time (microfluidics).
Normalize the microfluidOpen asset ↗SourceForge · disbac2-3-data-analysislines:168-214Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Image analysis is widely applied in plant science for phenotyping and monitoring botanic and agricultural species. Although a lot of software is available, tools integrating image analysis and statistical assessment of seedling growth in large groups of plants are limited or absent, and do not cover the needs of the researchers. In this study, we developed Morley, a free, open-source graphical user interface written in Python. Morley automates the following workflow: (1) group-wise analysis of a few thousand seedlings from multiple images; (2) recognition of seeds, shoots and roots in seedling images; (3) calculation of shoot and root lengths and surface areas, (4) evaluation of statistically significant differences between plant groups, (5) calculation of germination rates, (6) visualization and interpretation. Morley is designed for laboratory studies of biotic effects on seedling growth, when molecular mechanisms underlying morphometric changes are analyzed. Performance was tested using cultivars of T. aestivum, P. sativum on seedlings of up to 1 week old. Accuracy of the measured morphometric parameters was comparable with the ones obtained using ImageJ and manual measurements. Dose-dependent laboratory tests for germination affected by new bioactive compounds and fertilizers, assuming extraction of seedlings from a substrate and/or dissection are among the suggested applications.
Why it matches plant phenotyping methods植物の画像から種子・シュート・根を認識し、形態形質を自動抽出して統計評価するオープンソースツールの開発・精度検証が中心である。
abstractIn this study, we developed Morley, a free, open-source graphical user interface written in Python.
Reproduction assets foundThe paper's authors publicly released the Morley analysis code (GitHub repo dashabezik/Morley) and example data/user guide (dashabezik/plants), both explicitly stated in the Data Availability Statement and Methods. These directly support the paper's seedling image analysis and morphometric measurements.Code · publicths and plant surface areas, and figures characterizing
distributions of measured parameters, bar plots with mean values and standard deviations (95% CI),
and heatmaps visualizing the conclusions on statistical significance of the morphometric differences.
Code, graphical user interface, user guide and examples are available at
https://github.com/dashabezik/Morley and https://github.com/dashabezik/plants/, respectively.
Morley is available as a graphical user interface and a command line tool.
3. Results
3.1. Comparison of Morley with ImageJ and Manual Measurements Demonstrates Agreement between
Results
ImageJ [23] is widely applied for image analysis of plants and seedlings [24–28] andOpen asset ↗dashabezik/Morleypdf-layout-page:6 lines:1-47Dataset · publicon,
IAT; funding acquisition, IAT. All authors have read and agreed to the published version of the manuscript.
Funding: The study was supported by Russian Science Foundation, grant #22‐26‐00109.
Data Availability Statement: Program code, GUI, user guide and example data are available at
https://github.com/dashabezik/Morley and https://github.com/dashabezik/plants/.
Acknowledgments: The authors thank Dr. Olga M. Zhigalina and Dr. Dmitri N. Khmelenin (Shubnikov Institute
of Crystallography, FSRC “Crystallography and Photonics”, RAS) for collecting high‐quality TEM images of
iron nanoparticles and Dr. Nadezhda G. Berezkina (N.N. Semenov Federal Research Center for Chemical
Physics, RAS) forOpen asset ↗dashabezik/plantspdf-layout-page:13 lines:1-65Code / dataset availability confirmedCrossref · checked 8 Sept 2026
In today’s world, agricultural products are becoming increasingly scarce globally due to a variety of factors, and the early and accurate automatic identification of plant diseases can help ensure the stability and sustainability of agricultural production, improve the quality and safety of agricultural products, and help promote agricultural modernization and sustainable development. For this purpose, a lightweight deep isotropic convolutional neural network model, FoldNet, is designed for plant disease identification in this study. The model improves the architecture of residual neural networks by first folding the chain of the same blocks and then connecting these blocks with jump connections of different distances. Such a design allows the neural network to explore a larger receptive domain, enhancing its multiscale representation capability, increasing the direct propagation of information throughout the network, and improving the performance of the neural network. The FoldNet model achieved a recognition accuracy of 99.84% on the laboratory dataset PlantVillage using only 685k parameters and a recognition accuracy of 90.49% on the realistic scene dataset FGVC8 using only 516k parameters, which is competitive with other state-of-the-art models. In addition, as far as we know, our model is the first model that has fewer than 1M parameters while achieving state-of-the-art accuracy in plant disease identification. This proposal facilitates precision agriculture applications on mobile, low-end terminals.
Why it matches plant phenotyping methods植物画像から病害状態を識別する深層学習モデルの開発と複数データセットでの性能評価が中心であり、植物病害フェノタイピング手法に該当する。
abstracta lightweight deep isotropic convolutional neural network model, FoldNet, is designed for plant disease identification in this study.
Reproduction assets foundThe paper's plant-phenotyping inputs are two public plant disease image datasets (PlantVillage and FGVC8) explicitly declared as openly available in the Data Availability Statement. No author analysis code, trained model checkpoints, or paper-specific supplements with code are reported.Dataset · publicdataset referred to in this study is openly available at https://www.kaggle.com/competitions/plant-Open asset ↗www.kaggle.compdf-page:22 lines:1-60Code / dataset availability confirmedCrossref · checked 8 Sept 2026
Abstract Plant hydraulic conductivity and its decline under water stress are the focal point of current plant hydraulic research. The common methods of measuring hydraulic conductivity control a pressure gradient to push water through plant samples, submitting them to conditions far away from those that are experienced in nature where flow is suction driven and determined by the leaf water demand. In this paper, we present two methods for measuring hydraulic conductivity under closer to natural conditions, an artificial plant setup and a horizontal syringe pump setup. Both approaches use suction to pull water through a plant sample while dynamically monitoring the flow rate and pressure gradients. The syringe setup presented here allows for controlling and rapidly changing flow and pressure conditions, enabling experimental assessment of rapid plant hydraulic responses to water stress. The setup also allows quantification of dynamic changes in water storage of plant samples. Our tests demonstrate that the syringe pump setup can reproduce hydraulic conductivity values measured using the current standard method based on pushing water under above-atmospheric pressure. Surprisingly, using both the traditional and our new syringe pump setup, we found a positive correlation between changes in flow rate and hydraulic conductivity. Moreover, when flow or pressure conditions were changed rapidly, we found substantial contributions to flow by dynamic and largely reversible changes in the water storage of plant samples. Although the measurements can be performed under sub-atmospheric pressures, it is not possible to subject the samples to negative pressures due to the presence of gas bubbles near the valves and pressure sensors. Regardless, this setup allows for unprecedented insights into the interplay between pressure, flow rate, hydraulic conductivity and water storage in plant segments. This work was performed using an Open Science approach with the original data and analysis to be found at https://doi.org/10.5281/zenodo.7322605.
Why it matches plant phenotyping methods植物セグメントの水理伝導度と水貯蔵変化を自然条件に近く測定する新規セットアップを開発・検証しており、植物生理状態の取得手法が研究の中心である。
abstractIn this paper, we present two methods for measuring hydraulic conductivity under closer to natural conditions, an artificial plant setup and a horizontal syringe pump setup.
Reproduction assets foundThe paper explicitly states that all original data (hydraulic conductivity, flow, and pressure measurements) and the authors' analysis code are publicly available in a Zenodo deposit, cited twice (abstract and Data Availability statement).Dataset · publicAll data and analysis code is available at https://doi.org/10.5281/zenodo.7322605 .Open asset ↗Zenodo · 10.5281/zenodo.7322605lines:124-182Code / dataset availability confirmedCrossref · checked 8 Sept 2026
AppleArabidopsisLaboratory / benchtopMultispectral / hyperspectralLeafTissueClassificationObject detectionWater status / transpiration
Abstract Hyperhydricity (HH) is one of the most important physiological disorders that negatively affects various plant tissue culture techniques. The objective of this study was to characterize optical features to allow an automated detection of HH. For this purpose, HH was induced in two plant species, apple and Arabidopsis thaliana , and the severity was quantified based on visual scoring and determination of apoplastic liquid volume. The comparison between the HH score and the apoplastic liquid volume revealed a significant correlation, but different response dynamics. Corresponding leaf reflectance spectra were collected and different approaches of spectral analyses were evaluated for their ability to identify HH-specific wavelengths. Statistical analysis of raw spectra showed significantly lower reflection of hyperhydric leaves in the VIS, NIR and SWIR region. Application of the continuum removal hull method to raw spectra identified HH-specific absorption features over time and major absorption peaks at 980 nm, 1150 nm, 1400 nm, 1520 nm, 1780 nm and 1930 nm for the various conducted experiments. Machine learning (ML) model spot checking specified the support vector machine to be most suited for classification of hyperhydric explants, with a test accuracy of 85% outperforming traditional classification via vegetation index with 63% test accuracy and the other ML models tested. Investigations on the predictor importance revealed 1950 nm, 1445 nm in SWIR region and 415 nm in the VIS region to be most important for classification. The validity of the developed spectral classifier was tested on an available hyperspectral image acquisition in the SWIR-region.
Why it matches plant phenotyping methods植物組織培養におけるハイパーヒドリシティという植物状態を、分光計測と機械学習で自動検出・分類する手法を開発し、別のハイパースペクトル画像取得で妥当性検証しているため。
abstractThe objective of this study was to characterize optical features to allow an automated detection of HH.
Reproduction assets foundThe paper's RGB image dataset of hyperhydric in vitro explants (used for CNN-based HH detection) is publicly available on Roboflow, explicitly stated in the Data availability section and cited as Bethge (2023). Spectral datasets and trained spectral classifier are only available on request.Dataset · publicRGB image dataset analysed during the current study available in the Bethge ( 2023 ) repository, [ https://universe.roboflow.com/hains/hh-detection-in-vitro/dataset/8 ].Open asset ↗Roboflow · hh-detection-in-vitrolines:203-234Code / dataset availability confirmedOpenAlex · Europe PMC · Crossref · checked 7 Sept 2026
Plant traits are informative for ecosystem functions and processes and help to derive general rules and predictions about responses to environmental gradients, global change and perturbations. Ecological field studies often use 'low-throughput' methods to assess plant phenotypes and integrate species-specific traits to community-wide indices. In contrast, agricultural greenhouse or lab-based studies often employ 'high-throughput phenotyping' to assess plant individuals tracking their growth or fertilizer and water demand. In ecological field studies, remote sensing makes use of freely movable devices like satellites or unmanned aerial vehicles (UAVs) which provide large-scale spatial and temporal data. Adopting such methods for community ecology on a smaller scale may provide novel insights on the phenotypic properties of plant communities and fill the gap between traditional field measurements and airborne remote sensing. However, the trade-off between spatial resolution, temporal resolution and scope of the respective study requires highly specific setups so that the measurements fit the scientific question. We introduce small-scale, high-resolution digital automated phenotyping as a novel source of quantitative trait data in ecological field studies that provides complementary multi-faceted data of plant communities. We customized an automated plant phenotyping system for its mobile application in the field for 'digital whole-community phenotyping' (DWCP), capturing the 3-dimensional structure and multispectral information of plant communities. We demonstrated the potential of DWCP by recording plant community responses to experimental land-use treatments over two years. DWCP captured changes in morphological and physiological community properties in response to mowing and fertilizer treatments and thus reliably informed about changes in land-use. In contrast, manually measured community-weighted mean traits and species composition remained largely unaffected and were not informative about these treatments. DWCP proved to be an efficient method for characterizing plant communities, complements other methods in trait-based ecology, provides indicators of ecosystem states, and may help to forecast tipping points in plant communities often associated with irreversible changes in ecosystems.
Why it matches plant phenotyping methods植物群集の3次元構造とマルチスペクトル情報を取得する自動フェノタイピングシステムをフィールド用に改変・実証しており、植物表現型取得法が研究の中心である。
abstractWe introduce small-scale, high-resolution digital automated phenotyping as a novel source of quantitative trait data in ecological field studies
Reproduction assets foundThe paper's Data availability statement points to a public repository DOI (10.17616/R32P9Q, a re3data registry DOI) for the datasets presented in this study, which include the DWCP scan-derived morphological/physiological parameters, manual trait measurements, and vegetation data. No author analysis code or trained模型的公Dataset · publicThe datasets presented in this study can be found in online
repositories. The names of the repository/repositories and accession
number(s) can be found below: http://doi.org/10.17616/R32P9Q.Open asset ↗10.17616/R32P9Qpdf-page:11 lines:1-61Code / dataset availability confirmedEurope PMC · Crossref · checked 14 Sept 2026
Background The current development of sensor technologies towards ever more cost-effective and powerful systems is steadily increasing the application of low-cost sensors in different horticultural sectors. In plant in vitro culture, as a fundamental technique for plant breeding and plant propagation, the majority of evaluation methods to describe the performance of these cultures are based on destructive approaches, limiting data to unique endpoint measurements. Therefore, a non-destructive phenotyping system capable of automated, continuous and objective quantification of in vitro plant traits is desirable. Results An automated low-cost multi-sensor system acquiring phenotypic data of plant in vitro cultures was developed and evaluated. Unique hardware and software components were selected to construct a xyz-scanning system with an adequate accuracy for consistent data acquisition. Relevant plant growth predictors, such as projected area of explants and average canopy height were determined employing multi-sensory imaging and various developmental processes could be monitored and documented. The validation of the RGB image segmentation pipeline using a random forest classifier revealed very strong correlation with manual pixel annotation. Depth imaging by a laser distance sensor of plant in vitro cultures enabled the description of the dynamic behavior of the average canopy height, the maximum plant height, but also the culture media height and volume. Projected plant area in depth data by RANSAC (random sample consensus) segmentation approach well matched the projected plant area by RGB image processing pipeline. In addition, a successful proof of concept for in situ spectral fluorescence monitoring was achieved and challenges of thermal imaging were documented. Potential use cases for the digital quantification of key performance parameters in research and commercial application are discussed. Conclusion The technical realization of "Phenomenon" allows phenotyping of plant in vitro cultures under highly challenging conditions and enables multi-sensory monitoring through closed vessels, ensuring the aseptic status of the cultures. Automated sensor application in plant tissue culture promises great potential for a non-destructive growth analysis enhancing commercial propagation as well as enabling research with novel digital parameters recorded over time.
Why it matches plant phenotyping methods植物組織培養の形質を自動・非破壊・連続測定するマルチセンサーフェノタイピングシステムを開発し、画像分割や深度計測を検証しており、方法が研究の中心である。
abstractAn automated low-cost multi-sensor system acquiring phenotypic data of plant in vitro cultures was developed and evaluated.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicThe dataset supporting the conclusions of this article (Hard- and Software of “Phenomenon” phenotyping system) are available in an open-access Github repository, https://github.com/halube/Phenomenon .Open asset ↗halube/Phenomenonlines:224-282Code / dataset availability confirmedOpenAlex · Europe PMC · Crossref · checked 7 Sept 2026
Abstract Background Object detection, size determination, and colour detection of optical images are tools commonly used in plant science. Key examples of this include identification of ripening stages of fruit such as tomatoes and the determination of chlorophyll content as an indicator of plant health. While methods exist for determining these important phenotypes, they often require proprietary software or require coding knowledge to adapt existing code. Results We provide a set of free and open-source Python scripts that, without any adaptation, are able to perform background correction and colour correction on images using a ColourChecker chart. Further scripts identify objects, use an object of known size to calibrate for size, and extract the average colour of objects in RGB, Lab, and YUV colour spaces. We use two examples to demonstrate the use of these scripts. We show the consistency of these scripts by imaging in four different lighting conditions, and then we use two examples to show how the scripts can be used. In the first example, we estimate the lycopene content in tomatoes (Solanum lycopersicum) var. Tiny Tim using fruit images and an exponential model to predict lycopene content. We demonstrate that three different cameras (a DSLR camera and two separate mobile phones) are all able to model lycopene content. The models that predict lycopene or chlorophyll need to be adjusted depending on the camera used. In the second example, we estimate the chlorophyll content of basil (Ocimum basilicum) using leaf images and an exponential model to predict chlorophyll content. Conclusion A fast, cheap, non-destructive, and inexpensive method is provided for the determination of the size and colour of plant materials using a rig consisting of a lightbox, camera, and colour checker card and using free and open-source scripts that run in Python 3.8. This method accurately predicted the lycopene content in tomato fruit and the chlorophyll content in basil leaves.
Why it matches plant phenotyping methods植物画像からサイズ・色を抽出し、リコペンおよびクロロフィル含量を推定するオープンソース手法と画像取得系を開発・実証しており、植物フェノタイピング手法が中心である。
abstractWe provide a set of free and open-source Python scripts that, without any adaptation, are able to perform background correction and colour correction on images using a ColourChecker chart.
Reproduction assets foundThe paper provides authors' public Python scripts for plant image colour/size phenotyping on GitHub, plus a public data deposit (University of Sheffield repository DOI) and an OSF snapshot containing all scripts and data.Code · publicCustom Python Scripts: https://github.com/HarryCWright/PlantSizeClrOpen asset ↗HarryCWright/PlantSizeClrlines:62-83Code · publicSnapshot of all scripts and data is available on Open Science Framework: DOI: 10.17605/OSF.IO/QAYMUOpen asset ↗10.17605/OSF.IO/QAYMUlines:62-83Code / dataset availability confirmedEurope PMC · checked 7 Sept 2026
Background Live imaging is the gold standard for determining how cells give rise to organs. However, tracking many cells across whole organs over large developmental time windows is extremely challenging. In this work, we provide a comparably simple method for confocal live imaging entire Arabidopsis thaliana first leaves across early development. Our imaging method works for both wild-type leaves and the complex curved leaves of the jaw-1D mutant. Results We find that dissecting the cotyledons, affixing a coverslip above the samples and mounting samples with perfluorodecalin yields optimal imaging series for robust cellular and organ level analysis. We provide details of our complementary image processing steps in MorphoGraphX software for segmenting, tracking lineages, and measuring a suite of cellular properties. We also provide MorphoGraphX image processing scripts we developed to automate analysis of segmented images and data presentation. Conclusions Our imaging techniques and processing steps combine into a robust imaging pipeline. With this pipeline we are able to examine important nuances in the cellular growth and differentiation of jaw-D versus WT leaves that have not been demonstrated before. Our pipeline is approachable and easy to use for leaf development live imaging.
Why it matches plant phenotyping methodsArabidopsis葉の生細胞イメージング、画像処理、細胞追跡・形質測定を統合した再利用可能な表現型解析パイプラインの開発が中心である。
abstractIn this work, we provide a comparably simple method for confocal live imaging entire Arabidopsis thaliana first leaves across early development.
Reproduction assets foundThe paper publicly deposits its live-imaging datasets (confocal imaging data for the figures) on OSF under CC-BY 4.0, and its MorphoGraphX/R analysis scripts on the authors' GitHub repositories, all explicitly linked in the Availability of data and materials section.Dataset · publicData for Figs. 1 , 2 , 3 , 4 , 5 A, B is available at https://doi.org/10.17605/OSF.IO/V2TKWOpen asset ↗OSF · 10.17605/OSF.IO/V2TKWlines:139-172Dataset · publicData for Figs. 5 C, 6 and 7 is available at https://doi.org/10.17605/OSF.IO/D7X3YOpen asset ↗OSF · 10.17605/OSF.IO/D7X3Ylines:139-172Code · publicavailable at https://github.com/kateharline/live_img_paper , https://github.com/kateharline/roeder_lab_projects/tree/master/imagej_scripts and https://github.com/kateharline/jawd-paperOpen asset ↗github.com/kateharline/roeder_lab_projectslines:139-172Code · publicavailable at https://github.com/kateharline/live_img_paper , https://github.com/kateharline/roeder_lab_projects/tree/master/imagej_scripts and https://github.com/kateharline/jawd-paperOpen asset ↗github.com/kateharline/jawd-paperlines:139-172Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Lodging impedes the successful cultivation of cereal crops. Complex anatomy, morphology and environmental interactions make identifying reliable and measurable traits for breeding challenging. Therefore, we present a unique collaboration among disciplines for plant science, modelling and simulations, and experimental fluid dynamics in a broader context of breeding lodging resilient wheat and oat. We ran comprehensive wind tunnel experiments to quantify the stem bending behaviour of both cereals under controlled aerodynamic conditions. Measured phenotypes from experiments concluded that the wheat stems response is stiffer than the oat. However, these observations did not in themselves establish causal relationships of this observed behaviour with the physical traits of the plants. To further investigate we created an independent finite-element simulation framework integrating our recently developed multi-scale material modelling approach to predict the mechanical response of wheat and oat stems. All the input parameters including chemical composition, tissue characteristics and plant morphology have a strong physiological meaning in the hierarchical organization of plants, and the framework is free from empirical parameter tuning. This feature of our simulation framework reveals the multi-scale origin of the observed wide differences in the stem strength of both cereals that would not have been possible with purely experimental approach.
Why it matches plant phenotyping methods風洞実験と有限要素シミュレーションを統合し、植物茎の曲げ挙動・強度という表現型を予測・説明する手法が研究の中心である。
abstractWe ran comprehensive wind tunnel experiments to quantify the stem bending behaviour of both cereals under controlled aerodynamic conditions.
Reproduction assets foundThe paper's wind tunnel plant phenotyping assets are publicly available: raw wind tunnel videos of the cereal plants (DRUM repository), the authors' video-analysis scripts (GitHub), and the multi-scale finite-element model code (Dryad). Supplementary material with sample video and analysis details is on Figshare.Code · publiche scripts used and location of the data analysed from the wind tunnel experiment. Multi-scale material model codes in Python, Abaqus model file and python script for automatized simulations at different wind speed levels pertaining to multi-scale finite-element model simulations are available from the Dryad Digital Repository: https://doi.org/10.5061/dryad.612jm644j [ 53 ].
Supplementary material is available online [ 54 ].
Authors' contributionsOpen asset ↗Dryad Digital Repository · 10.5061/dryad.612jm644jlines:229-239Code / dataset availability confirmedEurope PMC · checked 8 Sept 2026
Background Cyst nematodes are one of the major groups of plant-parasitic nematode, responsible for considerable crop losses worldwide. Improving genetic resources, and therefore resistant cultivars, is an ongoing focus of many pest management strategies. One of the major bottlenecks in identifying the plant genes that impact the infection, and thus the yield, is phenotyping. The current available screening method is slow, has unidimensional quantification of infection limiting the range of scorable parameters, and does not account for phenotypic variation of the host. The ever-evolving field of computer vision may be the solution for both the above-mentioned issues. To utilise these tools, a specialised imaging platform is required to take consistent images of nematode infection in quick succession. Results Here, we describe an open-source, easy to adopt, imaging hardware and trait analysis software method based on a pre-existing nematode infection screening method in axenic culture. A cost-effective, easy-to-build and -use, 3D-printed imaging device was developed to acquire images of the root system of Arabidopsis thaliana infected with the cyst nematode Heterodera schachtii, replacing costly microscopy equipment. Coupling the output of this device to simple analysis scripts allowed the measurement of some key traits such as nematode number and size from collected images, in a semi-automated manner. Additionally, we used this combined solution to quantify an additional trait, root area before infection, and showed both the confounding relationship of this trait on nematode infection and a method to account for it. Conclusion Taken together, this manuscript provides a low-cost and open-source method for nematode phenotyping that includes the biologically relevant nematode size as a scorable parameter, and a method to account for phenotypic variation of the host. Together these tools highlight great potential in aiding our understanding of nematode parasitism.
Why it matches plant phenotyping methods根系感染像の取得プラットフォームと画像解析ソフトウェアを開発し、線虫数・サイズや感染前根面積を測定する手法が研究の中心であるため。
abstractwe describe an open-source, easy to adopt, imaging hardware and trait analysis software method
Reproduction assets foundThe paper's authors publicly release the imaging tower hardware design (STL files) and all ImageJ/Python analysis scripts used for nematode counting, root area quantification, and colour normalization in a GitHub repository, explicitly stated in the Availability of data and materials section.Code · publicAll scripts used in this experiment are available under the following github repository: https://github.com/OlafKranse/A_low_cost_imaging_tower .Open asset ↗OlafKranse/A_low_cost_imaging_towerlines:141-197Code / dataset availability confirmedEurope PMC · checked 8 Sept 2026
RiceLaboratory / benchtopX-ray / CTRootImage / point-cloud registrationGrowth / time-series analysisTrackingGrowth / development / phenologyRoot system architecture
Background Root system architecture (RSA) is an essential characteristic for efficient water and nutrient absorption in terrestrial plants; its plasticity enables plants to respond to different soil environments. Better understanding of root plasticity is important in developing stress-tolerant crops. Non-invasive techniques that can measure roots in soils nondestructively, such as X-ray computed tomography (CT), are useful to evaluate RSA plasticity. However, although RSA plasticity can be measured by tracking individual root growth, only a few methods are available for tracking individual roots from time-series three-dimensional (3D) images. Results We developed a semi-automatic workflow that tracks individual root growth by vectorizing RSA from time-series 3D images via two major steps. The first step involves 3D alignment of the time-series RSA images by iterative closest point registration with point clouds generated by high-intensity particles in potted soils. This alignment ensures that the time-series RSA images overlap. The second step consists of backward prediction of vectorization, which is based on the phenomenon that the root length of the RSA vector at the earlier time point is shorter than that at the last time point. In other words, when CT scanning is performed at time point A and again at time point B for the same pot, the CT data and RSA vectors at time points A and B will almost overlap, but not where the roots have grown. We assumed that given a manually created RSA vector at the last time point of the time series, all RSA vectors except those at the last time point could be automatically predicted by referring to the corresponding RSA images. Using 21 time-series CT volumes of a potted plant of upland rice (Oryza sativa), this workflow revealed that the root elongation speed increased with age. Compared with a workflow that does not use backward prediction, the workflow with backward prediction reduced the manual labor time by 95%. Conclusions We developed a workflow to efficiently generate time-series RSA vectors from time-series X-ray CT volumes. We named this workflow 'RSAtrace4D' and are confident that it can be applied to the time-series analysis of RSA development and plasticity.
Why it matches plant phenotyping methods根系形態を時系列X線CT画像から抽出・追跡する半自動ワークフローを開発しており、植物フェノタイピング手法が研究の中心である。
abstractWe developed a semi-automatic workflow that tracks individual root growth by vectorizing RSA from time-series 3D images via two major steps.
Reproduction assets foundThe paper's authors publicly released RSAtrace4D, the software implementing the backward-prediction workflow for time-series X-ray CT root system architecture analysis, on GitHub, and state that the datasets used are available via their GitHub account and project homepage.Code · publicThe implementation of this workflow, which is specified for rice, was named RSAtrace4D and is available at the GitHub repository ( https://github.com/st707311g/RSAtrace4D ).Open asset ↗st707311g/RSAtrace4Dlines:116-124Dataset · publicThe datasets used in this study are available at the GitHub repository ( https://github.com/st707311g/ ) and the project homepage ( https://rootomics.dna.affrc.go.jp/en/ ).Open asset ↗st707311glines:136-191Code / dataset availability confirmedOpenAlex · Europe PMC · Crossref · checked 8 Sept 2026
BACKGROUND: High-throughput phenotyping is crucial for the genetic and molecular understanding of adaptive root system development. In recent years, imaging automata have been developed to acquire the root system architecture of many genotypes grown in Petri dishes to explore the Genetic x Environment (GxE) interaction. There is now an increasing interest in understanding the dynamics of the adaptive responses, such as the organ apparition or the growth rate. However, due to the increasing complexity of root architectures in development, the accurate description of the topology, geometry, and dynamics of a growing root system remains a challenge. RESULTS: We designed a high-throughput phenotyping method, combining an imaging device and an automatic analysis pipeline based on registration and topological tracking, capable of accurately describing the topology and geometry of observed root systems in 2D + t. The method was tested on a challenging Arabidopsis seedling dataset, including numerous root occlusions and crossovers. Static phenes are estimated with high accuracy ([Formula: see text] and [Formula: see text] for primary and second-order roots length, respectively). These performances are similar to state-of-the-art results obtained on root systems of equal or lower complexity. In addition, our pipeline estimates dynamic phenes accurately between two successive observations ([Formula: see text] for lateral root growth). CONCLUSIONS: We designed a novel method of root tracking that accurately and automatically measures both static and dynamic parameters of the root system architecture from a novel high-throughput root phenotyping platform. It has been used to characterise developing patterns of root systems grown under various environmental conditions. It provides a solid basis to explore the GxE interaction controlling the dynamics of root system architecture adaptive responses. In future work, our approach will be adapted to a wider range of imaging configurations and species.
Why it matches plant phenotyping methods根系の静的・動的形質を画像から自動抽出する高スループット手法と解析パイプラインを開発・検証しており、表現型取得法が研究の中心である。
abstractWe designed a high-throughput phenotyping method, combining an imaging device and an automatic analysis pipeline based on registration and topological tracking
Reproduction assets foundThe paper's root reconstruction/phenotyping pipeline (RootSystemTracker) is released as open-source code on GitHub with an ImageJ plugin documentation page; an example time-lapse movie of the reconstruction is also available on YouTube. No public dataset of the 1000 time-lapse images or RSML outputs is stated in thesupCode · publicThe architecture reconstruction pipeline is supplied as an ImageJ plugin with online documentation (Plugin page: https://imagej.net/plugins/rootsystemtracker [ 9 ]) and as open-source code on GitHub ( https://github.com/Rocsg/RootSystemTracker ).Open asset ↗Rocsg/RootSystemTrackerlines:208-277Code / dataset availability confirmedEurope PMC · bioRxiv · checked 15 Sept 2026
Live imaging is the gold standard for determining how cellular development gives rise to organs. However, tracking all individual cells across whole organs over large developmental time windows is extremely challenging. In this work, we provide a comparably simple method for confocal live imaging of Arabidopsis thaliana first leaves across early development. Our imaging method works for both wild-type leaves and the complex curved leaves of the jaw-1D mutant. We find that dissecting the cotyledons, affixing a coverslip above the samples and mounting samples with perfluorodecalin yields optimal imaging series for robust cellular and organ level analysis. We provide details of our complementary image processing steps in MorphGraphX software for segmenting cells, tracking the cell lineages, and measuring a suite of cellular growth properties. We also provide MorphoGraphX image processing scripts that we developed to automate analysis of segmented images and data presentation. Our imaging techniques and processing steps combine into a robust imaging pipeline. With this pipeline we are able to examine important nuances in the cellular growth and differentiation of jaw-D versus WT leaves that have not been demonstrated before. Our pipeline is a practical starting place for researchers new to live imaging plant leaves, but also to anyone interested in improving the throughput and reliability of their live imaging process.
Why it matches plant phenotyping methods葉全体の共焦点ライブイメージング、細胞セグメンテーション・系譜追跡・成長特性測定を統合した実用的な表現型解析パイプラインの開発であり、方法が研究の中心です。
abstractIn this work, we provide a comparably simple method for confocal live imaging of Arabidopsis thaliana first leaves across early development.
Reproduction assets foundThe paper's phenotyping analysis code is publicly available in authors' GitHub repositories: MorphoGraphX processing/quantification scripts (iterative_growth_and_measures.py, multi_resize.py, batch_tiff.py) in roeder_lab_projects/mgx_scripts, ImageJ scripts, and R analysis/figure scripts in live_img_paper and jawdPaperCode · publice heat map representations of the
data with standardized parameters across time point comparisons and replicates (Video 4).
Data analysis
All data processing, analysis and plotting was performed in RStudio (2020; 2021). Scripts used
to process the data and create figures are enclosed as Supplemental Information and available at
https://github.com/kateharline/live_img_paper, https://github.com/kateharline/roeder_lab_proj-ects/tree/master/imagej_scripts and https://github.com/kateharline/jawd-paper.Data availability
Imaging data will be deposited XXXX.
Funding
Kate Harline was supported by NSF Graduate Research Fellowship (DGE-1650441). This work
was funded by NSF MCB-2203275 (AHKR), The SchwaOpen asset ↗kateharline/live_img_paperpdf-raw-page:20 lines:1-63Code · publicndardized parameters across time point comparisons and replicates (Video 4).
Data analysis
All data processing, analysis and plotting was performed in RStudio (2020; 2021). Scripts used
to process the data and create figures are enclosed as Supplemental Information and available at
https://github.com/kateharline/live_img_paper, https://github.com/kateharline/roeder_lab_proj-ects/tree/master/imagej_scripts and https://github.com/kateharline/jawd-paper.Data availability
Imaging data will be deposited XXXX.
Funding
Kate Harline was supported by NSF Graduate Research Fellowship (DGE-1650441). This work
was funded by NSF MCB-2203275 (AHKR), The Schwartz Research Fund Award (AHKR), and
the NationaOpen asset ↗kateharline/roeder_lab_proj-ectspdf-raw-page:20 lines:1-63Code · publicnalysis
All data processing, analysis and plotting was performed in RStudio (2020; 2021). Scripts used
to process the data and create figures are enclosed as Supplemental Information and available at
https://github.com/kateharline/live_img_paper, https://github.com/kateharline/roeder_lab_proj-ects/tree/master/imagej_scripts and https://github.com/kateharline/jawd-paper.Data availability
Imaging data will be deposited XXXX.
Funding
Kate Harline was supported by NSF Graduate Research Fellowship (DGE-1650441). This work
was funded by NSF MCB-2203275 (AHKR), The Schwartz Research Fund Award (AHKR), and
the National Institute Of General Medical Sciences of the National Institutes of Health under
Open asset ↗kateharline/jawd-paperpdf-raw-page:20 lines:1-63Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Premise The agar-based culture of Arabidopsis seedlings is widely used for quantifying root traits. Shoot traits are generally overlooked in these studies, probably because the rosettes are often askew. A technique to assess the shoot surface area of seedlings grown inside agar culture dishes would facilitate simultaneous root and shoot phenotyping. Methods We developed an image processing workflow in Python that estimates rosette area of Arabidopsis seedlings on agar culture dishes. We validated this method by comparing its output with other metrics of seedling growth. As part of a larger study on genetic variation in plant responses to nitrogen form and concentration, we measured the rosette areas from more than 2000 plate images. Results The rosette area measured from plate images was strongly correlated with the rosette area measured from directly overhead and moderately correlated with seedling mass. Rosette area in the large image set was significantly influenced by genotype and nitrogen treatment. The broad-sense heritability of leaf area measured using this method was 0.28. Discussion These results indicated that this approach for estimating rosette area produces accurate shoot phenotype data. It can be used with image sets for which other methods of leaf area quantification prove unsuitable.
Why it matches plant phenotyping methodsArabidopsis幼苗のロゼット面積という植物形質を画像から推定するPython画像処理ワークフローを開発・検証しており、表現型取得手法が研究の中心である。
abstractWe developed an image processing workflow in Python that estimates rosette area of Arabidopsis seedlings on agar culture dishes.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicThe workflows for each image set can be found at https://github.com/massivejords/Agar-plate-leaf-area as Jupyter Notebooks (Kluyver et al., 2016 ), along with the batch analysis Python script used to process the large image set.Open asset ↗massivejords/Agar-plate-leaf-arealines:85-97Code / dataset availability confirmedOpenAlex · Europe PMC · Crossref · checked 14 Sept 2026
High temperatures inhibit plant growth. A proposed strategy for improving plant productivity under elevated temperatures is the use of plant growth-promoting rhizobacteria (PGPR). While the effects of PGPR on plant shoots have been extensively explored, roots—particularly their spatial and temporal dynamics—have been hard to study, due to their below-ground nature. Here, we characterized the time- and tissue-specific morphological changes in bacterized plants using a novel non-invasive high-resolution plant phenotyping and imaging platform—GrowScreen-Agar II. The platform uses custom-made agar plates, which allow air exchange to occur with the agar medium and enable the shoot to grow outside the compartment. The platform provides light protection to the roots, the exposure of it to the shoots, and the non-invasive phenotyping of both organs. Arabidopsis thaliana, co-cultivated with Paraburkholderia phytofirmans PsJN at elevated and ambient temperatures, showed increased lengths, growth rates, and numbers of roots. However, the magnitude and direction of the growth promotion varied depending on root type, timing, and temperature. The root length and distribution per depth and according to time was also influenced by bacterization and the temperature. The shoot biomass increased at the later stages under ambient temperature in the bacterized plants. The study offers insights into the timing of the tissue-specific, PsJN-induced morphological changes and should facilitate future molecular and biochemical studies on plant–microbe–environment interactions.
Why it matches plant phenotyping methodsGrowScreen-Agar IIという非侵襲的な高解像度フェノタイピング・イメージングプラットフォームを用い、根とシュートの形態を時空間的に測定することが研究の中心的手法です。
abstractwe characterized the time- and tissue-specific morphological changes in bacterized plants using a novel non-invasive high-resolution plant phenotyping and imaging platform—GrowScreen-Agar II.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Supplement · publicThe following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/plants11212927/s1 , Figure S1: WinRhizo analyzed root lengths and root and shoot biomass; Figure S2: Root sampling and bacterial colonization confirmation; Figure S3: Sample root images generated by the GrowScreen-Agar II; Figure S4: Agar plates for GrowScreen-Agar II; Figure S5: Magazines for GrowScreen-Agar II; Figure S6: Imaging station of GrowScreen-Agar II; Table S1: Mean values and standard error of different root type morphological traits; Table S2: Mean values and standard error of different root system traits describing distribution and spread.Open asset ↗lines:106-120Code / dataset availability confirmedEurope PMC · checked 8 Sept 2026
Capturing cell-to-cell signals in a three-dimensional (3D) environment is key to studying cellular functions. A major challenge in the current culturing methods is the lack of accurately capturing multicellular 3D environments. In this study, we established a framework for 3D bioprinting plant cells to study cell viability, cell division, and cell identity. We established long-term cell viability for bioprinted Arabidopsis and soybean cells. To analyze the generated large image datasets, we developed a high-throughput image analysis pipeline. Furthermore, we showed the cell cycle reentry of bioprinted cells for which the timing coincides with the induction of core cell cycle genes and regeneration-related genes, ultimately leading to microcallus formation. Last, the identity of bioprinted Arabidopsis root cells expressing endodermal markers was maintained for longer periods. The framework established here paves the way for a general use of 3D bioprinting for studying cellular reprogramming and cell cycle reentry toward tissue regeneration.
Why it matches plant phenotyping methods植物細胞の3Dバイオプリンティング枠組みと、大規模画像から生存性・細胞分裂・細胞同一性を解析する高スループット画像解析パイプラインを開発しており、表現型取得・解析が研究の中心的な技術的貢献である。
abstractIn this study, we established a framework for 3D bioprinting plant cells to study cell viability, cell division, and cell identity.
Reproduction assets foundThe paper's authors publicly released their high-throughput confocal z-stack cell quantification pipeline (Python scripts wrapped in an R Shiny GUI), used to analyze the paper's bioprinted plant cell imaging datasets, on GitHub with a Zenodo deposit (10.5281/zenodo.7012765). The Zenodo record 5537065 in allowed_urls isCode · publicScripts for our high-throughput and automatic image analysis are available at https://github.com/LisaVdB/Confocal-z-stack-cell-detection and 10.5281/zenodo.7012765 .Open asset ↗LisaVdB/Confocal-z-stack-cell-detection · 10.5281/zenodo.7012765lines:247-261Code / dataset availability confirmedOpenAlex · Europe PMC · Crossref · checked 8 Sept 2026
Currently, there are no free databases of 3D point clouds and images for seedling phenotyping. Therefore, this paper describes a platform for seedling scanning using 3D Lidar with which a database was acquired for use in plant phenotyping research. In total, 362 maize seedlings were recorded using an RGB camera and a SICK LMS4121R-13000 laser scanner with angular resolutions of 45° and 0.5° respectively. The scanned plants are diverse, with seedling captures ranging from less than 10 cm to 40 cm, and ranging from 7 to 24 days after planting in different light conditions in an indoor setting. The point clouds were processed to remove noise and imperfections with a mean absolute precision error of 0.03 cm, synchronized with the images, and time-stamped. The database includes the raw and processed data and manually assigned stem and leaf labels. As an example of a database application, a Random Forest classifier was employed to identify seedling parts based on morphological descriptors, with an accuracy of 89.41%.
Why it matches plant phenotyping methods3D LiDARとRGBによる苗のスキャン基盤を開発し、植物フェノタイピング用データベースを構築・検証しているため、取得手法と再利用可能なデータセットが中心である。
abstractthis paper describes a platform for seedling scanning using 3D Lidar with which a database was acquired for use in plant phenotyping research.
Reproduction assets foundThe paper's maize seedling LiDAR phenotyping database (362 plants, 7 campaigns, raw/processed point clouds with stem/leaf labels, RGB images, rosbags) is publicly released on OSF across seven campaign-specific repositories, explicitly stated in the Data Availability Statement and Table 3. The GitHub links (sick_scan, uDataset · publicOur generated dataset is available online at: 1st campaign: https://osf.io/fcgwk/ ;Open asset ↗osf · fcgwklines:435-442Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
Submergence during germination impedes aerobic metabolisms and limits the growth of most higher plants. However, some wetland plants including rice can germinate under submerged conditions. It has long been hypothesized that the first elongating shoot tissue, the coleoptile, acts as a snorkel to acquire atmospheric oxygen (O 2 ) to initiate the first leaf elongation and seminal root emergence. Here, we obtained direct evidence for this hypothesis by visualizing the spatiotemporal O 2 dynamics during submerged germination in rice using a planar O 2 optode system. In parallel with the O 2 imaging, we tracked the anatomical development of shoot and root tissues in real-time using an automated flatbed scanner. Three hours after the coleoptile tip reached the water surface, O 2 levels around the embryo transiently increased. At this time, the activity of alcohol dehydrogenase (ADH), an enzyme critical for anaerobic metabolism, was significantly reduced, and the coleorhiza covering the seminal roots in the embryo was broken. Approximately 10 h after the transient burst in O 2 , seminal roots emerged. A transient O 2 burst around the embryo was shown to be essential for seminal root emergence during submerged rice germination. The parallel application of a planar O 2 optode system and automated scanning system can be a powerful tool for examining how environmental conditions affect germination in rice and other plants.
Why it matches plant phenotyping methods水中イネ発芽時の酸素動態と器官発達を、平面O2オプトードおよび自動スキャナーで時空間的に可視化・追跡する手法が研究の中心であり、植物の生理状態・形態発達を測定する実質的なフェノタイピング手法である。
abstractvisualizing the spatiotemporal O 2 dynamics during submerged germination in rice using a planar O 2 optode system.
Reproduction assets foundThe paper's phenotyping measurements (time-lapse growth images and planar optode O2 imaging of submerged rice germination) are publicly available as Supplementary Videos 1–3 hosted at the Frontiers supplementary material URL. No author analysis code or trained models are deposited; ImageJ and UWSC are generic third‑dayDataset · publicof their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2022.946776/full#supplementary-material
Supplementary Video 1
Time-lapse images showing the germination process of submerged rice with normoxic or anoxic atmospheres.
Click here for additional data file.
Supplementary Video 2
Time-lapse images of the growth process following a shift from an anoxic to a normoxic atmosphOpen asset ↗lines:107-237Code / dataset availability confirmedEurope PMC · checked 8 Sept 2026
Background Characterizing plant genetic resources and their response to the environment through accurate measurement of relevant traits is crucial to genetics and breeding. Spatial organization of the maize ear provides insights into the response of grain yield to environmental conditions. Current automated methods for phenotyping the maize ear do not capture these spatial features. Results We developed EARBOX, a low-cost, open-source system for automated phenotyping of maize ears. EARBOX integrates open-source technologies for both software and hardware that facilitate its deployment and improvement for specific research questions. The imaging platform consists of a customized box in which ears are repeatedly imaged as they rotate via motorized rollers. With deep learning based on convolutional neural networks, the image analysis algorithm uses a two-step procedure: ear-specific grain masks are first created and subsequently used to extract a range of trait data per ear, including ear shape and dimensions, the number of grains and their spatial organisation, and the distribution of grain dimensions along the ear. The reliability of each trait was validated against ground-truth data from manual measurements. Moreover, EARBOX derives novel traits, inaccessible through conventional methods, especially the distribution of grain dimensions along grain cohorts, relevant for ear morphogenesis, and the distribution of abortion frequency along the ear, relevant for plant response to stress, especially soil water deficit. Conclusions The proposed system provides robust and accurate measurements of maize ear traits including spatial features. Future developments include grain type and colour categorisation. This method opens avenues for high-throughput genetic or functional studies in the context of plant adaptation to a changing environment.
Why it matches plant phenotyping methodsトウモロコシ雌穂の画像取得・深層学習による形質抽出システムを開発し、手動測定との比較で各形質の信頼性を検証しており、植物フェノタイピング手法が研究の中心です。
abstractWe developed EARBOX, a low-cost, open-source system for automated phenotyping of maize ears.
Reproduction assets foundThe authors' full analysis pipeline (MATLAB GUI plus Python deep-learning code for grain segmentation and phenotypic trait extraction) is explicitly stated to be fully available on a public GitHub repository. The phenotype datasets themselves are only available on request, so they do not qualify as public assets.Code · publicThe code for the analysis using a Graphical User Interface in MATLAB is fully available on a public repository ( https://github.com/Phymea-Systems/Earbox ). It is used in combination with a Python code applying the trained neural network to extract the DL2 images, also available in the same public repository.Open asset ↗Phymea-Systems/Earboxlines:104-113Code / dataset availability confirmedEurope PMC · bioRxiv · checked 15 Sept 2026
Background Cyst nematodes are one of the major groups of plant-parasitic nematode, responsible for considerable crop losses worldwide. Improving genetic resources, and therefore resistant cultivars, is an ongoing focus of many pest management strategies. One of the major bottlenecks in identifying the plant genes that impact the infection, and thus the yield, is phenotyping. The current available screening method is slow, has unidimensional quantification of infection limiting the range of scorable parameters, and does not account for phenotypic variation of the host. The ever-evolving field of computer vision may be the solution for both the above-mentioned issues. To utilise these tools, a specialised imaging platform is required to take consistent images of nematode infection in quick succession. Results Here, we describe an open-source, easy to adopt, imaging hardware and trait analysis software method based on a pre-existing nematode infection screening method in axenic culture. A cost-effective, easy-to-build and -use, 3D-printed imaging device was developed to acquire images of the root system of Arabidopsis thaliana infected with the cyst nematode Heterodera schachtii , replacing costly microscopy equipment. Coupling the output of this device to simple analysis scripts allowed the measurement of some key traits such as nematode number and size from collected images, in a semi-automated manner. Additionally, we used this combined solution to quantify an additional trait, root area before infection, and showed both the confounding relationship of this trait on nematode infection and a method to account for it. Conclusion Taken together, this manuscript provides a low-cost and open-source method for nematode phenotyping that includes the biologically relevant nematode size as a scorable parameter, and a method to account for phenotypic variation of the host. Together these tools highlight great potential in aiding our understanding of nematode parasitism.
Why it matches plant phenotyping methods植物寄生性線虫感染の画像取得・解析を自動化する低コストの装置とソフトウェアを開発し、線虫数・サイズおよび根面積を測定する手法が中心であるため。
abstractHere, we describe an open-source, easy to adopt, imaging hardware and trait analysis software method
Reproduction assets foundThe paper's ImageJ analysis scripts (root surface area, colored-agar variant, leaf surface count) and a custom Python color-normalization script are explicitly deposited in the authors' public GitHub repository (OlafKranse/A_low_cost_imaging_tower), directly reproducing this paper's phenotyping analysis. No phenotype/тCode · publici.org/10.1101/2022.07.14.500020; this version posted July 15, 2022. The copyright holder for this preprint
(which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is
made available under a CC-BY 4.0 International license.
described in the script
(https://github.com/OlafKranse/A_low_cost_imaging_tower/blob/main/Imaging and
Analyses/automated_root_surface_area.ijm). A slightly adjusted script was used for plates
containing dye (https://github.com/OlafKranse/A_low_cost_imaging_tower/blob/main/Imaging and
Analyses/automated_root_surface_area_colored_agar.ijm). The root surface area for all the images
in the folderOpen asset ↗OlafKranse/A_low_cost_imaging_towerpdf-layout-page:6 lines:1-37Code · publicing and quantifiable traits
Automatic counting was performed on images taken as described above. Depending on the
treatment a different script was used to calculate the number and size of females. Before isolation,
the colour histogram for all images was normalised to the first image in the dataset using a custom
python script (https://github.com/OlafKranse/A_low_cost_imaging_tower/tree/main/Imaging and
Analyses/Normalise colour). The images were then processed in ImageJ for two different nematode
life stages: i) tanned cyst nematodes; ii) female nematodes.Open asset ↗OlafKranse/A_low_cost_imaging_towerpdf-layout-page:6 lines:1-37Code / dataset availability confirmedEurope PMC · checked 8 Sept 2026
Background and aims Seed germination is strongly influenced by environmental temperatures. With global temperatures predicted to rise, the timing of germination for thousands of plant species could change, leading to potential decreases in fitness and ecosystem-wide impacts. The thermogradient plate (TGP) is a powerful but underutilized research tool that tests germination under a broad range of constant and alternating temperatures, giving researchers the ability to predict germination characteristics using current and future climates. Previously, limitations surrounding experimental design and data analysis methods have discouraged its use in seed biology research. Methods Here, we have developed a freely available R script that uses TGP data to analyse seed germination responses to temperature. We illustrate this analysis framework using three example species: Wollemia nobilis, Callitris baileyi and Alectryon subdentatus. The script generates >40 germination indices including germination rates and final germination across each cell of the TGP. These indices are then used to populate generalized additive models and predict germination under current and future monthly maximum and minimum temperatures anywhere on the globe. Key results In our study species, modelled data were highly correlated with observed data, allowing confident predictions of monthly germination patterns for current and future climates. Wollemia nobilis germinated across a broad range of temperatures and was relatively unaffected by predicted future temperatures. In contrast, C. baileyi and A. subdentatus showed strong seasonal temperature responses, and the timing for peak germination was predicted to shift seasonally under future temperatures. Conclusions Our experimental workflow is a leap forward in the analysis of TGP experiments, increasing its many potential benefits, thereby improving research predictions and providing substantial information to inform management and conservation of plant species globally.
Why it matches plant phenotyping methods熱勾配プレート実験の種子発芽表現型を解析・予測するRスクリプトとワークフローが中心で、観測値との検証も行っているため。
abstractwe have developed a freely available R script that uses TGP data to analyse seed germination responses to temperature.
Reproduction assets foundThe paper's TGP germination data and R analysis workflow are openly deposited on Zenodo (record 5457222), with explicit availability statements in the Methods and Data Availability sections.Dataset · publicThe data that support the findings of this study are openly available in Zenodo at https://doi.org/10.5281/zenodo.5457222 .Open asset ↗Zenodo · 10.5281/zenodo.5457222lines:223-251Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
The existing methods of callose quantification include epifluorescence microscopy and fluorescence spectrophotometry of aniline blue-stained callose particles, immuno-fluorescence microscopy and indirect assessment of both callose synthase and β-(1,3)-glucanase enzyme activities. Some of these methods are laborious, time consuming, not callose-specific, biased and require high technical skills. Here, we describe a method of callose quantification based on Sandwich Enzyme-Linked Immunosorbent Assay (S-ELISA). Tissue culture-derived banana plantlets were inoculated with Xanthomonas campestris pv. musacearum ( Xcm ) bacteria as a biotic stress factor inducing callose production. Banana leaf, pseudostem and corm tissue samples were collected at 14 days post-inoculation (dpi) for callose quantification. Callose levels were significantly different in banana tissues of Xcm -inoculated and control groups except in the pseudostems of both banana genotypes. The method described here could be applied for the quantification of callose in different plant species with satisfactory level of specificity to callose, and reproducibility. Additionally, the use of 96-well plate makes this method suitable for high throughput callose quantification studies with minimal sampling and analysis biases. We provide step-by-step detailed descriptions of the method.
Why it matches plant phenotyping methods植物組織中のカロース量を定量するELISA法を開発・再現性評価し、高スループット測定への適用性を示した研究であり、植物状態の取得方法が中心です。
abstractHere, we describe a method of callose quantification based on Sandwich Enzyme-Linked Immunosorbent Assay (S-ELISA).
Reproduction assets foundThe paper's supplementary material (Table S1) publicly hosts the callose quantification measurements (concentrations in leaves, pseudostems, corms of Xcm-inoculated vs. control banana plantlets) underlying this study's analysis. No author analysis code, images, or trained models are deposited; the R statistical packageDataset · publicor up to 12 months).
Dissolve para-nitrophenyl phosphate (pNPP) in substrate buffer to a working concentration of 1 mg/mL.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/mps5040054/s1 , Table S1: Analysis of callose concentration in the leaves, pseudostems and corms of banana plants inoculated and non-inoculated (control) with Xcm (Independent sample t-test, α ≤ 0.05).
Click here for additional data file.
Author Contributions
Conceptualization, A.K.T.; methodology, A.S.M., A.K.T. and P.S.; validatiOpen asset ↗lines:167-297Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Duckweeds, a group of floating aquatic plants, are ideal model plants for laboratory experiments because they are small, easy to cultivate, and reproduce quickly. Duckweed laboratory biology, however, requires that lineages are maintained as continuous populations of asexually propagating fronds, so research teams need to calibrate cultivation conditions and coordinate maintenance tasks for duckweed stocks. Computational image data analysis is proving a powerful duckweed research tool, but researchers lack software tools to assist with data collection and storage in a way that can feed into scripted data analysis. We set out to support these processes — cultivation, and subsequent integration with data analysis tools — using a laboratory management software called Aquarium, an open-source application developed to manage laboratory inventory and plan experiments. We developed a suite of duckweed cultivation and experimentation operation types in Aquarium, which we then integrated with novel data analysis scripts. We then demonstrated the efficacy of our system with a series of image-based growth assays, and explored how our framework could be used to calibrate cultivation protocols. We discuss the unexpected advantages and the limitations of this approach, suggesting areas for future software tool development. In its current state, our approach helps to bridge the gap between laboratory implementation and data analytical software for duckweed biologists and builds a foundation for future development of end-to-end computational tools in plant science.
Why it matches plant phenotyping methodsアヒルウキクサの画像ベース成長アッセイと解析スクリプトを統合するオープンソースの実験・データ管理ワークフローを開発・実証しており、植物表現型取得と解析基盤が中心である。
abstractComputational image data analysis is proving a powerful duckweed research tool, but researchers lack software tools to assist with data collection and storage in a way that can feed into scripted data analysis.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Dataset · publicExperimental
data and analysis scripts can be downloaded from the Github directory
(https://github.com/mtscott321/duckweed_data_analysis).Open asset ↗mtscott321/duckweed_data_analysispdf-page:4 lines:1-47Code / dataset availability confirmedbioRxiv · checked 8 Sept 2026
X-ray fluorescence spectroscopy (XRF) is a powerful technique for the in vivo assessment of plant tissues. However, the potential X-ray exposure damages might affect the structure and elemental composition of living plant tissues leading to artefacts in the recorded data. Herein, we exposed soybean (Glycine max (L.) Merrill) leaves to several X-ray doses through a polychromatic benchtop microprobe X-ray fluorescence spectrometer, modulating the photon flux by adjusting either the beam size, focus, or exposure time. The structure, ultrastructure and physiological responses of the irradiated plant tissues were investigated through light and transmission electron microscopy (TEM). Depending on the dose, the X-ray exposure induced decreased K and X-ray scattering intensities, and increased Ca, P, and Mn signals on soybean leaves. Anatomical analysis indicated necrosis of the epidermal and mesophyll cells on the irradiated spots, where TEM images revealed the collapse of cytoplasm and cell-wall breaking. Furthermore, the histochemical analysis detected the production of reactive oxygen species, as well as inhibition of chlorophyll autofluorescence in these areas. Under certain X-ray exposure conditions, e.g., high photon flux and exposure time, XRF measurements may affect the soybean leaves structures, elemental composition, and cellular ultrastructure, and induce programmed cell death. These results shed light on the characterization of the radiation damage, and thus, help to assess the X-ray radiation limits and strategies for in vivo for XRF analysis. HighlightBy exposing soybean leaves to several X-ray doses, we show that the characteristic X-ray induced elemental changes stem from plants physiological signalling or responses rather than only sample dehydration.
Why it matches plant phenotyping methods植物組織のin vivo XRF測定における放射線損傷と測定アーティファクトを評価し、適用限界と測定条件を検証する研究であり、フェノタイピング手法の技術的妥当性が中心です。
abstractX-ray fluorescence spectroscopy (XRF) is a powerful technique for the in vivo assessment of plant tissues.
Reproduction assets foundThe paper's DATA AVAILABILITY section states the raw data (XRF spectra/maps and imaging measurements) are fully available on Figshare at the authors' public DOI, which matches an allowed URL.Dataset · publicThe raw data herein presented is fully available at Figshare
repository: https://doi.org/10.6084/m9.figshare.1858438Open asset ↗Figshare · 10.6084/m9.figshare.1858438pdf-page:6 lines:1-93Code / dataset availability confirmedEurope PMC · bioRxiv · checked 15 Sept 2026
Biological systems are the sum of their dynamic 3-dimensional (3D) parts. Therefore, it is critical to study biological structures in 3D and at high resolutions to gain insights into their physiological functions. Electron microscopy of metal replicas of unroofed cells and isolated organelles has been a key technique to visualize intracellular structures at nanometer resolution. However, many of these protocols require specialized equipment and personnel to complete them. Here we present novel accessible protocols to analyze biological structures in unroofed cells and biochemically isolated organelles in 3D and at nanometer resolutions, focusing on Arabidopsis clathrin-coated vesicles (CCVs) - an essential trafficking organelle lacking detailed structural characterization due to their low preservation in classical electron microscopy techniques. First, we establish a protocol to visualize CCVs in unroofed cells using scanning-transmission electron microscopy (STEM) tomography, providing sufficient resolution to define the clathrin coat arrangements. Critically, the samples are prepared directly on electron microscopy grids, removing the requirement to use extremely corrosive acids, thereby enabling the use of this protocol in any electron microscopy lab. Secondly, we demonstrate this standardized sample preparation allows the direct comparison of isolated CCV samples with those visualized in cells. Finally, to facilitate the high-throughput and robust screening of metal replicated samples, we provide a deep learning analysis workflow to screen the ‘pseudo 3D’ morphology of CCVs imaged with 2D modalities. Overall, we present accessible ways to examine the 3D structure of biological samples and provide novel insights into the structure of plant CCVs.
Why it matches plant phenotyping methods植物細胞内オルガネラの3D形態を取得・解析する電子顕微鏡プロトコルと深層学習ワークフローが研究の中心であり、植物CCV形態の技術的スクリーニング手法を提供している。
abstractHere we present novel accessible protocols to analyze biological structures in unroofed cells and biochemically isolated organelles in 3D and at nanometer resolutions, focusing on Arabidopsis clathrin-coated vesicles (CCVs)
Reproduction assets foundThe paper's Data Availability statement explicitly deposits example data (SEM replica images, training image pairs) and the analysis code (Cellpose-based CCV segmentation workflow) generated in this study at a public Zenodo DOI, making it a paper-specific, publicly actionable asset. The temography.com URLs are vendor/mCode · publicand round; LF, large and
354
flat) using an area threshold of 8500 nm2
(a CCV diameter of 105 nm) and a 3D value of 1.52 (the
355
average of the 3 smallest CCVs in control conditions determined to be spherical by the experimenter).
356
Data Availability
357
Example data and the code generated in this study is available at:
358
https://doi.org/10.5281/zenodo.6563819
359
Acknowledgements
360
This research was supported by the Scientific Service Units of Institute of Science and Technology
361
Austria (ISTA) through resources provided by the Electron Microscopy Facility, Lab Support Facility and
362
the Imaging and Optics Facility. A.J. is supported by funding from the Austrian Science FundOpen asset ↗zenodo · 10.5281/zenodo.6563819pdf-raw-page:12 lines:1-46Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Large-scale investigations of maize kernel traits important to researchers, breeders, and processors require high throughput methods, which are presently lacking. To address this bottleneck, we developed a novel flatbed platform that automatically acquires and analyzes multiwavelength near-infrared (NIR hyperspectral) images of maize kernels precisely enough to support robust predictions of protein content, density, and endosperm vitreousness. The upward facing-camera design and the automated ability to analyze the embryo or abgerminal sides of each individual kernel in a sample with the appropriate side-specific model helped to produce a superior combination of throughput and prediction accuracy compared to other single-kernel platforms. Protein was predicted to within 0.85% (root mean square error of prediction), density to within 0.038 g/cm 3 , and endosperm vitreousness percentage to within 6.3%. Kernel length and width were also accurately measured so that each kernel in a rapidly scanned sample was comprehensively characterized.
Why it matches plant phenotyping methodsトウモロコシ穀粒の組成・物理形質を高スループットに取得・推定するハイパースペクトル画像プラットフォームと解析手法の開発が研究の中心である。
abstractwe developed a novel flatbed platform that automatically acquires and analyzes multiwavelength near-infrared (NIR hyperspectral) images of maize kernels
Reproduction assets foundThe paper's authors explicitly state that all analysis code for the hyperspectral phenotyping pipeline (PLSR trait prediction, PLS-DA kernel-side classification, image analysis) is publicly available in their GitHub repository.Code · publicgenerate a confusion
matrix, along with specificity and sensitivity rates (Supplemental
Table 1).
2.7. Complete pipeline
The processes, measurements, and analyses described in Sections
2.3-2.6 were combined to produce a pipeline shown in Fig. 1B-E. All of
the code created to execute the analyses is available in this repository,
https://github.com/jivarelao/Hyperspectral_Scanner.3. Results and discussion
3.1. Variability of maize kernel traits in ground-truth sets
Directly measured traits ranged widely across the kernel samples
(Table 1). Kernel volume displayed the largest range (5.6-fold). Kernel
weight was second at 5-fold, followed by vitreousness (2.7-fold), protein
(2.4-fold) and densitOpen asset ↗https://github.com/jivarelao/Hyperspectral_Scanner.3pdf-raw-page:5 lines:1-77Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Background Quinoa is an increasingly popular seed crop frequently studied for its tolerance to various abiotic stresses as well as its susceptibility to heat. Estimations of quinoa pollen viability through staining methods have resulted in conflicting results. A more effective alternative to stains is to estimate pollen viability through in vitro germination. Here we report a method for in vitro quinoa pollen germination that could be used to understand the impact of various stresses on quinoa fertility and therefore seed yield or to identify male-sterile lines for breeding. Results A semi-automated method to count germinating pollen was developed in PlantCV, which can be widely used by the community. Pollen collected on day 4 after first anthesis at zeitgeber time 5 was optimum for pollen germination with an average germination of 68% for accession QQ74 (PI 614886). The optimal length of pollen incubation was found to be 48 h, because it maximizes germination rates while minimizing contamination. The pollen germination medium's pH, boric acid, and sucrose concentrations were optimized. The highest germination rates were obtained with 16% sucrose, 0.03% boric acid, 0.007% calcium nitrate, and pH 5.5. This medium was tested on quinoa accessions QQ74, and cherry vanilla with 68%, and 64% germination efficiencies, respectively. Conclusions We provide an in vitro pollen germination method for quinoa with average germination rates of 64 and 68% on the two accessions tested. This method is a valuable tool to estimate pollen viability in quinoa, and to test how stress affects quinoa fertility. We also developed an image analysis tool to semi-automate the process of counting germinating pollen. Quinoa produces many new flowers during most of its panicle development period, leading to significant variation in pollen maturity and viability between different flowers of the same panicle. Therefore, collecting pollen at 4 days after first anthesis is very important to collect more uniformly developed pollen and to obtain high germination rates.
Why it matches plant phenotyping methodsキノア花粉の生存性を測定するin vitro発芽法を開発・最適化し、PlantCVによる発芽花粉の半自動画像計数も開発しており、植物形質取得法が中心である。
abstractA semi-automated method to count germinating pollen was developed in PlantCV, which can be widely used by the community.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産2件を確認しました。Code · publicThis workflow is available at https://github.com/danforthcenter/quinoa-pollen-germination and a tutorial is availabe at https://github.com/danforthcenter/plantcv-tutorial-interactive-pollent-count .Open asset ↗GitHub · danforthcenter/quinoa-pollen-germinationlines:134-159Code · publicThis workflow is available at https://github.com/danforthcenter/quinoa-pollen-germination and a tutorial is availabe at https://github.com/danforthcenter/plantcv-tutorial-interactive-pollent-count .Open asset ↗GitHub · danforthcenter/plantcv-tutorial-interactive-pollent-countlines:134-159Code / dataset availability confirmedOpenAlex · Europe PMC · checked 14 Sept 2026
BACKGROUND: Although quantitative single-cell analysis is frequently applied in animal systems, e.g. to identify novel drugs, similar applications on plant single cells are largely missing. We have exploited the applicability of high-throughput microscopic image analysis on plant single cells using tobacco leaf protoplasts, cell-wall free single cells isolated by lytic digestion. Protoplasts regenerate their cell wall within several days after isolation and have the potential to expand and proliferate, generating microcalli and finally whole plants after the application of suitable regeneration conditions. RESULTS: High-throughput automated microscopy coupled with the development of image processing pipelines allowed to quantify various developmental properties of thousands of protoplasts during the initial days following cultivation by immobilization in multi-well-plates. The focus on early protoplast responses allowed to study cell expansion prior to the initiation of proliferation and without the effects of shape-compromising cell walls. We compared growth parameters of wild-type tobacco cells with cells expressing the antiapoptotic protein Bcl2-associated athanogene 4 from Arabidopsis (AtBAG4). CONCLUSIONS: AtBAG4-expressing protoplasts showed a higher proportion of cells responding with positive area increases than the wild type and showed increased growth rates as well as increased proliferation rates upon continued cultivation. These features are associated with reported observations on a BAG4-mediated increased resilience to various stress responses and improved cellular survival rates following transformation approaches. Moreover, our single-cell expansion results suggest a BAG4-mediated, cell-independent increase of potassium channel abundance which was hitherto reported for guard cells only. The possibility to explain plant phenotypes with single-cell properties, extracted with the single-cell processing and analysis pipeline developed, allows to envision novel biotechnological screening strategies able to determine improved plant properties via single-cell analysis.
Why it matches plant phenotyping methods植物プロトプラストの成長・増殖特性を大量画像から抽出する自動顕微鏡解析と画像処理パイプラインを開発・適用しており、表現型取得手法が研究の中心である。
abstractHigh-throughput automated microscopy coupled with the development of image processing pipelines allowed to quantify various developmental properties of thousands of protoplasts
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicAll the scripts and codes used in the analysis pipeline, additional downloaded plugins used in processing the images as well as sample data can be found in our Github page https://github.com/jodawson/cell_seg_tracking_analysis .Open asset ↗jodawson/cell_seg_tracking_analysislines:143-159Code / dataset availability confirmedbioRxiv · Europe PMC · checked 8 Sept 2026
O_LIMore than ever, ecologists seek to employ herbarium collections to estimate plant functional traits from the past and across biomes. However, many trait measurements are destructive, which may preclude their use on valuable specimens. Researchers increasingly use reflectance spectroscopy to estimate traits from fresh or ground leaves, and to delimit or identify taxa. Here, we extend this body of work to non-destructive measurements on pressed, intact leaves, like those in herbarium collections. C_LIO_LIUsing 618 samples from 68 species, we used partial least-squares regression to build models linking pressed-leaf reflectance spectra to a broad suite of traits, including leaf mass per area (LMA), leaf dry matter content (LDMC), equivalent water thickness, carbon fractions, pigments, and twelve elements. We compared these models to those trained on fresh- or ground-leaf spectra of the same samples. C_LIO_LIOur pressed-leaf models were best at estimating LMA (R2 = 0.932; %RMSE = 6.56), C (R2 = 0.855; %RMSE = 9.03), and cellulose (R2 = 0.803; %RMSE = 12.2), followed by water-related traits, certain nutrients (Ca, Mg, N, and P), other carbon fractions, and pigments (all R2 = 0.514-0.790; %RMSE = 12.8-19.6). Remaining elements were predicted poorly (R2 20). For most chemical traits, pressed-leaf models performed better than fresh-leaf models, but worse than ground-leaf models. Pressed-leaf models were worse than fresh-leaf models for estimating LMA and LDMC, but better than ground-leaf models for LMA. Finally, in a subset of samples, we used partial least-squares discriminant analysis to classify specimens among 10 species with near-perfect accuracy (>97%) from pressed- and ground-leaf spectra, and slightly lower accuracy (>93%) from fresh-leaf spectra. C_LIO_LIThese results show that applying spectroscopy to pressed leaves is a promising way to estimate leaf functional traits and identify species without destructive analysis. Pressed-leaf spectra might combine advantages of fresh and ground leaves: like fresh leaves, they retain some of the spectral expression of leaf structure; but like ground leaves, they circumvent the masking effect of water absorption. Our study has far-reaching implications for capturing the wide range of functional and taxonomic information in the worlds preserved plant collections. C_LI
Why it matches plant phenotyping methods押葉の反射分光から葉の機能形質を非破壊推定する手法を開発・比較検証しており、植物形質取得が研究の中心である。
abstractwe used partial least-squares regression to build models linking pressed-leaf reflectance spectra to a broad suite of traits
Reproduction assets foundThe paper's fresh-leaf spectral dataset is publicly available via the CABO data portal. Pressed/ground spectra, trait data, and PLSR/PLS-DA models are only promised 'upon publication' to EcoSIS and EcoSML, so those require contacting the authors; no author analysis code with a public URL is stated.Dataset · publicAll fresh-leaf spectral data are available through the CABO data portal (https://data.caboscience.org/leaf).Open asset ↗CABO data portalpdf-page:24 lines:1-32Code / dataset availability confirmedEurope PMC · Crossref · checked 8 Sept 2026
The wheat grain three-dimensional (3D) phenotypic characters are of great significance for final yield and variety breeding, and the ventral sulcus traits are the important factors to the wheat flour yield. The wheat grain trait measurements are necessary; however, the traditional measurement method is still manual, which is inefficient, subjective, and labor intensive; moreover, the ventral sulcus traits can only be obtained by destructive measurement. In this paper, an intelligent analysis method based on the structured light imaging has been proposed to extract the 3D wheat grain phenotypes and ventral sulcus traits. First, the 3D point cloud data of wheat grain were obtained by the structured light scanner, and then, the specified point cloud processing algorithms including single grain segmentation and ventral sulcus location have been designed; finally, 28 wheat grain 3D phenotypic characters and 4 ventral sulcus traits have been extracted. To evaluate the best experimental conditions, three-level orthogonal experiments, which include rotation angle, scanning angle, and stage color factors, were carried out on 125 grains of 5 wheat varieties, and the results demonstrated that optimum conditions of rotation angle, scanning angle, and stage color were 30°, 37°, black color individually. Additionally, the results also proved that the mean absolute percentage errors (MAPEs) of wheat grain length, width, thickness, and ventral sulcus depth were 1.83, 1.86, 2.19, and 4.81%. Moreover, the 500 wheat grains of five varieties were used to construct and validate the wheat grain weight model by 32 phenotypic traits, and the cross-validation results showed that the R 2 of the models ranged from 0.77 to 0.83. Finally, the wheat grain phenotype extraction and grain weight prediction were integrated into the specialized software. Therefore, this method was demonstrated to be an efficient and effective way for wheat breeding research.
Why it matches plant phenotyping methods構造化光画像から小麦粒の3D表現型と腹溝形質を抽出する手法を開発し、精度評価・条件最適化・ソフトウェア統合まで行っており、表現型取得が中心である。
abstractIn this paper, an intelligent analysis method based on the structured light imaging has been proposed to extract the 3D wheat grain phenotypes and ventral sulcus traits.
Reproduction assets found本文中に内容が明示された植物フェノタイピング関連の補足表と、その公開リンクを確認しました。Supplement · publicSupplementary Table 2
The original data of structured light imaging, X-ray CT, and manual measurements of 125 wheat grains.Open asset ↗lines:608-666Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
Capturing cell-to-cell and cell-to-environment signals in a defined 3 dimensional (3D) microenvironment is key to study cellular functions, including cellular reprogramming towards tissue regeneration. A major challenge in current culturing methods is that these methods cannot accurately capture this multicellular 3D microenvironment. In this study, we established the framework of 3D bioprinting with plant cells to study cell viability, cell division, and cell identity. We established long-term cell viability for bioprinted Arabidopsis root cells and soybean meristematic cells. To analyze the large image datasets generated during these long-term viability studies, we developed an open source high-throughput image analysis pipeline. Furthermore, we showed the cell cycle re-entry of the isolated Arabidopsis and soybean cells leading to the formation of microcalli. Finally, we showed that the identity of isolated cells of Arabidopsis roots expressing endodermal markers maintained longer periods of time. The framework established in this study paves the way for a general use of 3D bioprinting for studying cellular reprogramming and cell cycle re-entry towards tissue regeneration.
Why it matches plant phenotyping methods植物細胞の3Dバイオプリンティング系と、長期画像データから細胞生存性・分裂・同一性を抽出するオープンソース解析パイプラインを開発しており、植物状態の取得・解析手法が中心である。
abstractIn this study, we established the framework of 3D bioprinting with plant cells to study cell viability, cell division, and cell identity.
Reproduction assets foundThe paper's authors publicly released their in-house confocal z-stack cell-counting image analysis pipeline (Python scripts wrapped in an R Shiny GUI) on GitHub, which directly reproduces the paper's computational analysis of bioprinted plant cell images. Generic dependencies (pyimageJ, OpenCV, ComDet, R shiny) and theCode · publicpipeline
contained in Python and further developed into an R Shiny application (44) can be easily accessed, along
with the usage instructions, from the Github repository at https://github.com/LisaVdB/Confocal-z-stack-
cell-detection.
Data availability
Scripts for our high-throughput and automatic image analysis are available at
https://github.com/LisaVdB/Confocal-z-stack-cell-detection.Open asset ↗LisaVdB/Confocal-z-stack-cell-detectionpdf-layout-page:10 lines:1-49Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
ArabidopsisLaboratory / benchtopRootMorphology / geometry measurementTrackingGrowth / development / phenologyRoot system architecture
Directional root growth control is crucial for plant fitness. The degree of root growth deviation depends on several factors, whereby exogenous growth conditions have a profound impact. The perception of mechanical impedance by wild-type roots results in the modulation of root growth traits, and it is known that gravitropic stimulus influences distinct root movement patterns in concert with mechanoadaptation. Mutants with reduced shootward auxin transport are described as being numb towards mechanostimulus and gravistimulus, whereby different growth conditions on agar-supplemented medium have a profound effect on how much directional root growth and root movement patterns differ between wild types and mutants. To reduce the impact of unilateral mechanostimulus on roots grown along agar-supplemented medium, we compared the root movement of Col-0 and auxin resistant 1-7 in a root penetration assay to test how both lines adjust the growth patterns of evenly mechanostimulated roots. We combined the assay with the D-root system to reduce light-induced growth deviation. Moreover, the impact of sucrose supplementation in the growth medium was investigated because exogenous sugar enhances root growth deviation in the vertical direction. Overall, we observed a more regular growth pattern for Col-0 but evaluated a higher level of skewing of aux1-7 compared to the wild type than known from published data. Finally, the tracking of the growth rate of the gravistimulated roots revealed that Col-0 has a throttling elongation rate during the bending process, but aux1-7 does not.
Why it matches plant phenotyping methodsD-rootシステムと根貫通アッセイを組み合わせ、根の成長パターン・伸長速度を追跡して評価する測定ワークフローが研究の中心であるため。
abstractWe combined the assay with the D-root system to reduce light-induced growth deviation.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Supplement · publicThe following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/plants11050650/s1 , Table S1: raw data.Open asset ↗lines:48-103Code / dataset availability confirmedCrossref · Europe PMC · checked 8 Sept 2026
Abstract Cassava brown streak disease (CBSD) is an emerging viral disease that can greatly reduce cassava productivity, while causing only mild aerial symptoms that develop late in infection. Early detection of CBSD enables better crop management and intervention. Current techniques require laboratory equipment and are labour intensive and often inaccurate. We have developed a handheld active multispectral imaging (A-MSI) device combined with machine learning for early detection of CBSD in real-time. The principal benefits of A-MSI over passive MSI and conventional camera systems are improved spectral signal-to-noise ratio and temporal repeatability. Information fusion techniques further combine spectral and spatial information to reliably identify features that distinguish healthy cassava from plants with CBSD as early as 28 days post inoculation on a susceptible and a tolerant cultivar. Application of the device has the potential to increase farmers’ access to healthy planting materials and reduce losses due to CBSD in Africa. It can also be adapted for sensing other biotic and abiotic stresses in real-world situations where plants are exposed to multiple pest, pathogen and environmental stresses.
Why it matches plant phenotyping methods植物のウイルス感染状態（病徴）を対象に、携帯型マルチスペクトル画像装置と空間・スペクトル機械学習を開発し、早期検出性能を示した研究であり、表現型取得法が中心です。
abstractWe have developed a handheld active multispectral imaging (A-MSI) device combined with machine learning for early detection of CBSD in real-time.
Reproduction assets foundThe article's Data availability statement explicitly deposits the paper's own multispectral imaging dataset (Cassava-TME204-UCBSV trials) on Zenodo. No author analysis code or trained models are stated as available.Dataset · publicThe MSI dataset of these three trials (Cassava-TME204-UCBSV) are available at https://doi.org/10.5281/zenodo.4636968 .Open asset ↗zenodo · 10.5281/zenodo.4636968lines:203-262Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Multispectral imaging is at the forefront of contactless surface analysis. Standard multispectral imaging systems use sophisticated software, cameras and light filtering optics. This paper discloses the building of a customizable and cost-effective multispectral imaging and analysis system. It integrates a web camera, light emitting diodes (LEDs) lighting, a semisphere for even lightening, an open-source Arduino™ development board and a free Python application to automatically obtain and visually analyze multispectral images. The device is hereafter called MEDUSA and its optical performance was tested for repeated Imaging consistency, visible and near infrared band sensitivity and lighting evenness. Four proof of concept tests were run in order to understand the advantageous use of this system, as compared to a simple visual score of diverse samples. Each of three qualitative tests used sets of 12 LED band spectral images to analyze ink changes in a counterfeit bill, surface bruises on Hass avocado fruits and transient changes in petri dish grown bacterial colonies. A fourth test used single band imaging in a set of standard laboratory analyzed plant samples, to quantitatively relate a red band light reflectance to its nitrogen content. These tests indicate that MEDUSA made images may yield qualitative and quantitative spectral information unseen to the naked eye, suggesting potential use in currency counterfeit tests, food quality analyses, microbial phenotyping and agricultural plant chemistry. MEDUSA can be freely reproduced and customized from this research, making it a powerful and affordable analytical tool to analyze a wide range of subtle chemical properties in samples at industrial and science fields.
Why it matches plant phenotyping methods植物試料の化学的状態を非接触画像から推定する低コスト multispectral imaging システムを開発し、光学性能を検証している。植物サンプルの反射率と窒素含量の定量関係も評価され、植物表現型取得への応用が明示されている。
abstractThis paper discloses the building of a customizable and cost-effective multispectral imaging and analysis system.
Reproduction assets foundThe paper discloses the MEDUSA multispectral imaging system with author-provided analysis/control code (Python GUI with PCA image analysis, Arduino firmware) publicly deposited on OSF. No standalone plant-phenotyping dataset (e.g., the nitrogen reflectance plant samples) is explicitly deposited; only the software/hardwCode · publicences
•
Environmental and agricultural sciences
•
Counterfeit detection
•
General surface analytical chemistry
Hardware type
•
Imaging tools
•
Field measurements and sensors
•
Electrical engineering and computer science
Open-Source License
GNU General Public License (GPL)
Cost of Hardware
Less than 300USD
Source File Repository
https://osf.io/zhp4m/
Hardware in context
Multispectral imaging is at the forefront of dry and non-invasive spatial analytical chemistry. It is used in fields as diverse as human health [9] , food quality [8] , plant science [22] soil chemistry [18] , counterfeit [7] and art analyses [15] . Despite its proven general value, wide access to these systOpen asset ↗OSFlines:1-59Code / dataset availability confirmedEurope PMC · checked 8 Sept 2026
Abstract Background: Quinoa is an increasingly popular seed crop frequently studied for its tolerance to various abiotic stresses as well as its susceptibility to heat. Estimations of quinoa pollen viability through staining methods have resulted in conflicting results. A more effective alternative to stains is to estimate pollen viability through in vitro germination. Here we report a method for in vitro quinoa pollen germination that could be used to understand the impact of various stresses on quinoa fertility and therefore seed yield or to identify male-sterile lines for breeding. Results: A semi-automated method to count germinating pollen was developed in PlantCV, which can be widely used by the community. Pollen collected on day 4 after first anthesis at ZT5 was optimum for pollen germination with an average germination of 68% for accession QQ74 (PI 614886). The optimal length of pollen incubation was found to be 48 hours, because it maximizes germination rates while minimizing contamination. The pollen germination medium’s pH, boric acid, and sucrose concentrations were optimized. The highest germination rates were obtained with 16% sucrose, 0.03% boric acid, 0.007% calcium nitrate, and pH 5.5. This medium was tested on quinoa accessions QQ74, and cherry vanilla with 68%, and 64% germination efficiencies, respectively. Conclusions: We provide an in vitro pollen germination method for quinoa with average germination rates of 64 and 68% on the two accessions tested. This method is a valuable tool to estimate pollen viability in quinoa, and to test how stress affects quinoa fertility. We also developed an image analysis tool to semi-automate the process of counting germinating pollen. Quinoa produces many new flowers during most of its panicle development period, leading to significant variation in pollen maturity and viability between different flowers of the same panicle. Therefore, collecting pollen at 4 days after first anthesis is very important to collect more uniformly developed pollen and to obtain high germination rates.
Why it matches plant phenotyping methodsキノア花粉の生存性を評価するin vitro発芽法を開発・最適化し、PlantCVによる発芽花粉の画像カウントも半自動化しており、植物形質取得法が研究の中心である。
abstractA semi-automated method to count germinating pollen was developed in PlantCV, which can be widely used by the community.
Reproduction assets foundThe paper's pollen germination microscopy images are deposited on Zenodo and the PlantCV analysis workflow/scripts plus extracted numerical data are on the authors' GitHub, both explicitly stated with URLs.Dataset · publicImages are available here:
https://doi.org/10.5281/zenodo.5909573.Open asset ↗Zenodo · 10.5281/zenodo.5909573pdf-page:9 lines:1-47Code · publicScripts and extracted numerical data are available on
GitHub: https://github.com/danforthcenter/quinoa-pollen-germination.Open asset ↗GitHub · danforthcenter/quinoa-pollen-germinationpdf-page:11 lines:1-46Code / dataset availability confirmedEurope PMC · Crossref · checked 15 Sept 2026
Capturing complete internal anatomies of plant organs and tissues within their relevant morphological context remains a key challenge in plant science. While plant growth and development are inherently multiscale, conventional light, fluorescence, and electron microscopy platforms are typically limited to imaging of plant microstructure from small flat samples that lack a direct spatial context to, and represent only a small portion of, the relevant plant macrostructures. We demonstrate technical advances with a lab-based X-ray microscope (XRM) that bridge the imaging gap by providing multiscale high-resolution three-dimensional (3D) volumes of intact plant samples from the cell to the whole plant level. Serial imaging of a single sample is shown to provide sub-micron 3D volumes co-registered with lower magnification scans for explicit contextual reference. High-quality 3D volume data from our enhanced methods facilitate sophisticated and effective computational segmentation. Advances in sample preparation make multimodal correlative imaging workflows possible, where a single resin-embedded plant sample is scanned via XRM to generate a 3D cell-level map, and then used to identify and zoom in on sub-cellular regions of interest for high-resolution scanning electron microscopy. In total, we present the methodologies for use of XRM in the multiscale and multimodal analysis of 3D plant features using numerous economically and scientifically important plant systems.
Why it matches plant phenotyping methods植物の細胞から個体レベルの3D形態を取得するX線顕微鏡法と試料調製・計算セグメンテーションを中心に開発・提示しており、植物表現型取得手法が明確に主題である。
abstractWe demonstrate technical advances with a lab-based X-ray microscope (XRM) that bridge the imaging gap by providing multiscale high-resolution three-dimensional (3D) volumes of intact plant samples from the cell to the whole plant level.
Reproduction assets foundThe authors deposited fly-through animations of 2D image stacks and 3D volume rendering animations of the XRM scans shown in the paper's figures on figshare, directly reproducing this paper's plant phenotyping imaging data. No author analysis code or trained model checkpoints were explicitly deposited.Dataset · publicCanada) was used for data integration, visualization, and animation of the scan data, and to export image data as 2D 16-bit Tag Image File Format (TIFF) stacks. Fly-through animations of 2D image stacks for scans shown in all Figures, as well as 3D volume rendering animations of selected scans, are available for download from ( https://figshare.com/s/944efc8832e47fd4f203 ).
Image analysis and segmentation
Data from XRM scans were segmented using Amira software and with the assistance of a Wacom tablet for manual segmentation, in addition to ORS Dragonfly Deep Learning Module 2021.1.0.977 which is free for noncommercial use. Segmentation for Figure 1D combined automated and manual methods in Open asset ↗figsharelines:87-114Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Background Most plants encounter water stress at one or more different stages of their life cycle. The maintenance of genetic stability is the integral component of desiccation tolerance that defines the storage ability and long-term survival of seeds. Embryonic axes of desiccation-sensitive recalcitrant seeds of Acer pseudoplatnus L. were used to investigate the genotoxic effect of desiccation. Alkaline single-cell gel electrophoresis (comet assay) methodology was optimized and used to provide unique insights into the onset and repair of DNA strand breaks and 8-oxo-7,8-dihydroguanine (8-oxoG) formation during progressive steps of desiccation and rehydration. Results The loss of DNA integrity and impairment of damage repair were significant predictors of the viability of embryonic axes. In contrast to the comet assay, automated electrophoresis failed to detect changes in DNA integrity resulting from desiccation. Notably, no significant correlation was observed between hydroxyl radical ( ٠ OH) production and 8-oxoG formation, although the former is regarded to play a major role in guanine oxidation. Conclusions The high-throughput comet assay represents a sensitive tool for monitoring discrete changes in DNA integrity and assessing the viability status in plant germplasm processed for long-term storage.
Why it matches plant phenotyping methods植物胚軸のDNA完全性と生存性を評価する高スループットコメットアッセイを最適化・検証しており、表現型状態の取得法が研究の中心である。
abstractAlkaline single-cell gel electrophoresis (comet assay) methodology was optimized and used to provide unique insights into the onset and repair of DNA strand breaks
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Supplement · publicAdditional file 3: Fig. S3. (download PDF )
The representative comet measurements and images captured by Comet Assay IV analysis software.Open asset ↗lines:516-614Code / dataset availability confirmedOpenAlex · Crossref · checked 15 Sept 2026
With the ongoing cost decrease of genotyping and sequencing technologies, accurate and fast phenotyping remains the bottleneck in the utilizing of plant genetic resources for breeding and breeding research. Although cost-efficient high-throughput phenotyping platforms are emerging for specific traits and/or species, manual phenotyping is still widely used and is a time- and money-consuming step. Approaches that improve data recording, processing or handling are pivotal steps towards the efficient use of genetic resources and are demanded by the research community. Therefore, we developed PhenoApp, an open-source Android app for tablets and smartphones to facilitate the digital recording of phenotypical data in the field and in greenhouses. It is a versatile tool that offers the possibility to fully customize the descriptors/scales for any possible scenario, also in accordance with international information standards such as MIAPPE (Minimum Information About a Plant Phenotyping Experiment) and FAIR (Findable, Accessible, Interoperable, and Reusable) data principles. Furthermore, PhenoApp enables the use of pre-integrated ready-to-use BBCH (Biologische Bundesanstalt für Land- und Forstwirtschaft, Bundessortenamt und CHemische Industrie) scales for apple, cereals, grapevine, maize, potato, rapeseed and rice. Additional BBCH scales can easily be added. The simple and adaptable structure of input and output files enables an easy data handling by either spreadsheet software or even the integration in the workflow of laboratory information management systems (LIMS). PhenoApp is therefore a decisive contribution to increase efficiency of digital data acquisition in genebank management but also contributes to breeding and breeding research by accelerating the labour intensive and time-consuming acquisition of phenotyping data.
Why it matches plant phenotyping methods植物表現型データのデジタル記録・取得を目的とするオープンソースアプリの開発であり、表現型測定ワークフローが中心的です。
abstractTherefore, we developed PhenoApp, an open-source Android app for tablets and smartphones to facilitate the digital recording of phenotypical data in the field and in greenhouses.
Reproduction assets foundThe paper describes PhenoApp, an open-source Android phenotyping app. Authors provide the app's source code (Gitea, archived on Zenodo) and underlying example input/output phenotype data files on Zenodo under CC0. The SHAPE II project website is a project page, not a paper-specific data deposit, and is excluded.Code · publice ‘in’ folder of the app main directory and no additional source data is required).
-
Output_example.xls (sample output file created by PhenoApp).
Data are available under the terms of the
Creative Commons Zero “No rights reserved” data waiver (CC0 1.0 Public domain dedication).
Software availability
Source code available from:
https://gitea.julius-kuehn.de/JKI/pheno-app
Archived source code at time of publication:
https://doi.org/10.5281/zenodo.5525779
36
License:
Apache-2.0
Acknowledgements
We are grateful to Moritz Cappel, Teresa Claus and Claudia Vogel for ongoing testing, recommendations and bug report of PhenoApp during development.
Funding Statement
This work was supported by grants fOpen asset ↗gitea.julius-kuehn.de · JKI/pheno-applines:333-433Code · publicput_example.xls (sample output file created by PhenoApp).
Data are available under the terms of the
Creative Commons Zero “No rights reserved” data waiver (CC0 1.0 Public domain dedication).
Software availability
Source code available from:
https://gitea.julius-kuehn.de/JKI/pheno-app
Archived source code at time of publication:
https://doi.org/10.5281/zenodo.5525779
36
License:
Apache-2.0
Acknowledgements
We are grateful to Moritz Cappel, Teresa Claus and Claudia Vogel for ongoing testing, recommendations and bug report of PhenoApp during development.
Funding Statement
This work was supported by grants from the German Federal Ministry of Education and Research to FS (SelWineQ, FKZ 031B0889Open asset ↗Zenodo · 10.5281/zenodo.5525779lines:333-433Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
In plants, secretion of cell wall components and membrane proteins plays a fundamental role in growth and development as well as survival in diverse environments. Exocytosis, as the last step of the secretory trafficking pathway, is a highly ordered and precisely controlled process involving tethering, docking, and fusion of vesicles at the plasma membrane (PM) for cargo delivery. Although the exocytic process and machinery are well characterized in yeast and animal models, the molecular players and specific molecular events that underpin late stages of exocytosis in plant cells remain largely unknown. Here, by using the delivery of functional, fluorescent-tagged cellulose synthase (CESA) complexes (CSCs) to the PM as a model system for secretion, as well as single-particle tracking in living cells, we describe a quantitative approach for measuring the frequency of vesicle tethering events. Genetic and pharmacological inhibition of cytoskeletal function, reveal that the initial vesicle tethering step of exocytosis is dependent on actin and myosin XI. In contrast, treatments with the microtubule inhibitor, oryzalin, did not significantly affect vesicle tethering or fusion during CSC exocytosis but caused a minor increase in transient or aborted tethering events. With data from this new quantitative approach and improved spatiotemporal resolution of single particle events during secretion, we generate a revised model for the role of the cortical cytoskeleton in CSC trafficking.
Why it matches plant phenotyping methods植物細胞内の小胞テザリング頻度を単一粒子追跡で定量する新しい測定手法を開発・適用しており、植物状態の取得・定量が研究の中心である。
abstractsingle-particle tracking in living cells, we describe a quantitative approach for measuring the frequency of vesicle tethering events.
Reproduction assets foundThe paper's supplementary materials include Video S1, a live-cell imaging movie of a CSC particle insertion event next to a cortical microtubule, which directly reproduces the paper's plant phenotyping (single-particle CSC trafficking) measurements. No author analysis code or datasets with explicit deposit language areSupplement · publicnt care and maintenance of plant materials and to all members of the Staiger laboratory for helpful discussions and input.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms23010317/s1 , Video S1: A CSC particle is inserted next to a cortical microtubule and translocates on the microtubule during the steady movement phase.
Click here for additional data file.
Author Contributions
W.Z. and C.J.S. designed the research. W.Z. performed the experiments and analyzed the data. W.Z. and C.J.S. wrote the Open asset ↗lines:64-115Code / dataset availability confirmedEurope PMC · checked 8 Sept 2026
RiceLaboratory / benchtopLiDAR / point cloudPanicle / ear / spikeSegmentation
The automated measurement of crop phenotypic parameters is of great significance to the quantitative study of crop growth. The segmentation and classification of crop point cloud help to realize the automation of crop phenotypic parameter measurement. At present, crop spike-shaped point cloud segmentation has problems such as fewer samples, uneven distribution of point clouds, occlusion of stem and spike, disorderly arrangement of point clouds, and lack of targeted network models. The traditional clustering method can realize the segmentation of the plant organ point cloud with relatively independent spatial location, but the accuracy is not acceptable. This paper first builds a desktop-level point cloud scanning apparatus based on a structured-light projection module to facilitate the point cloud acquisition process. Then, the rice ear point cloud was collected, and the rice ear point cloud data set was made. In addition, data argumentation is used to improve sample utilization efficiency and training accuracy. Finally, a 3D point cloud convolutional neural network model called Panicle-3D was designed to achieve better segmentation accuracy. Specifically, the design of Panicle-3D is aimed at the multiscale characteristics of plant organs, combined with the structure of PointConv and long and short jumps, which accelerates the convergence speed of the network and reduces the loss of features in the process of point cloud downsampling. After comparison experiments, the segmentation accuracy of Panicle-3D reaches 93.4%, which is higher than PointNet. Panicle-3D is suitable for other similar crop point cloud segmentation tasks.
Why it matches plant phenotyping methodsイネ穂の3D点群を取得・データセット化し、器官分割による表現型パラメータ測定のための装置と専用ニューラルネットワークを開発・評価しており、表現型取得・抽出手法が中心である。
abstractThe automated measurement of crop phenotypic parameters is of great significance to the quantitative study of crop growth.
Reproduction assets foundThe authors explicitly state that the Python code of the point cloud dataset and the Panicle-3D model is publicly available on GitHub, providing a paper-specific, actionable asset for the rice panicle point cloud segmentation analysis.Code · publicThe Python code of the point cloud dataset and model is available on Github at https://github.com/gitDux/Panicle-3D .Open asset ↗gitDux/Panicle-3Dlines:86-247Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
Stomatal observation and automatic stomatal detection are useful analyses of stomata for taxonomic, biological, physiological, and eco-physiological studies. We present a new clearing method for improved microscopic imaging of stomata in soybean followed by automated stomatal detection by deep learning. We tested eight clearing agent formulations based upon different ethanol and sodium hypochlorite (NaOCl) concentrations in order to improve the transparency in leaves. An optimal formulation-a 1:1 ( v / v ) mixture of 95% ethanol and NaOCl (6-14%)-produced better quality images of soybean stomata. Additionally, we evaluated fixatives and dehydrating agents and selected absolute ethanol for both fixation and dehydration. This is a good substitute for formaldehyde, which is more toxic to handle. Using imaging data from this clearing method, we developed an automatic stomatal detector using deep learning and improved a deep-learning algorithm that automatically analyzes stomata through an object detection model using YOLO. The YOLO deep-learning model successfully recognized stomata with high mAP (~0.99). A web-based interface is provided to apply the model of stomatal detection for any soybean data that makes use of the new clearing protocol.
Why it matches plant phenotyping methodsダイズ葉の気孔画像取得法と、気孔を自動検出・解析する深層学習手法を開発・評価しており、植物形質取得が研究の中心である。
abstractWe present a new clearing method for improved microscopic imaging of stomata in soybean followed by automated stomatal detection by deep learning.
Reproduction assets foundThe paper's soybean stomatal phenotype dataset (Table S2, manual vs. automatic stomatal density for 386 accessions) is publicly available via the MDPI supplement, and the trained YOLOv5 stomata-detection model is publicly served through the authors' web application. The 183-image training dataset and analysis code haveSupplement · publicnowledge the personnel from the Plant Genetics and Breeding lab at the Kyungpook National University for their time and work at the greenhouse.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Materials
The following are available online at https://www.mdpi.com/article/10.3390/plants10122714/s1 , Table S1: The representative methods for detecting stomata in different species, Table S2: Comparison stomata density between counting by manual and develped program.
Click here for additional data file.
Author Contributions
Conceptualization, J.-D.L. and Y.J.K.; methodology, S.N.S.; formal analysis, H.P., S.H.COpen asset ↗lines:69-162Code / dataset availability confirmedEurope PMC · checked 13 Sept 2026
The PFuji-Size dataset is comprised of a collection of 3D point clouds of Fuji apple trees ( Malus domestica Borkh. cv. Fuji) scanned at different maturity stages and annotated for fruit detection and size estimation. Structure-from-motion and multi-view stereo techniques were used to generate the 3D point clouds of 6 complete Fuji apple trees containing a total of 615 apples. The resulting point clouds were 3D segmented by identifying the 3D points corresponding to each apple (3D instance segmentation), obtaining a single point cloud for each apple. All segmented apples were labelled with ground truth diameter annotations. Since the data was acquired in field conditions and at different maturity stages, the set includes different fruit diameters -from 26.9 mm to 94.8 mm- and different fruit occlusion percentages due to foliage. In addition, 25 apples were photographed 360° in laboratory conditions, obtaining high resolution 3D point clouds of this sub-set. To the best of the authors' knowledge, this is the first publicly available dataset for apple size estimation in field conditions. This dataset was used to evaluate different fruit size estimation methods in the research article titled "In-field apple size estimation using photogrammetry-derived 3D point clouds: comparison of 4 different methods considering fruit occlusion" (Gené-Mola et al., 2021).
Why it matches plant phenotyping methodsリンゴ果実の3D画像・点群から果径を推定するための公開データセットであり、アノテーション、3Dセグメンテーション、サイズ推定評価が中心的な方法論的貢献である。
abstractThe PFuji-Size dataset is comprised of a collection of 3D point clouds of Fuji apple trees ( Malus domestica Borkh. cv. Fuji) scanned at different maturity stages and annotated for fruit detection and size estimation.
Reproduction assets foundThe paper is a Data in Brief article describing the PFuji-Size dataset (raw images, 3D tree point clouds, apple segmentation masks, diameter/centre annotations), publicly deposited in Dataverse (CSUC) with DOI 10.34810/data141 and a direct URL. This is a paper-specific, public, actionable phenotyping dataset directly.Dataset · publicData accessibility
Repository name: Dataverse
Data identification number: https://doi.org/10.34810/data141
DOI: https://doi.org/10.34810/data141
Direct URL to data: https://dataverse.csuc.cat/dataset.xhtml?persistentId=doi:10.34810/data141Open asset ↗Dataverse · doi:10.34810/data141lines:54-87Code / dataset availability confirmedCrossref · checked 9 Sept 2026
Significance The lack of suitable approaches for studying root–microbe interactions, live and in situ, has severely limited our ability to understand the rhizosphere. In this study, we overcome this major limitation with an imaging system that combines transparent soils with cutting edge light sheet microscopy. The study revealed that the root cap is a point of first contact for microbes before establishment and reveals how the pore structure influences the patterns of interactions between the microbe and the plant. With the combined use of light sheet microscopy and transparent soils, we shed light on previously unseen interaction phenomena and accelerate the understanding of how rhizospheres are formed.
Why it matches plant phenotyping methods透明土壌とライトシート顕微鏡を組み合わせたライブ・インサイチュ画像システムの開発が研究の中心で、根と微生物の相互作用という植物状態を可視化している。
abstractwe overcome this major limitation with an imaging system that combines transparent soils with cutting edge light sheet microscopy.
Reproduction assets foundThe paper deposits its phenotyping data (light-sheet microscopy volumes of root–soil–bacteria interactions) on Zenodo, makes its image analysis software (MATLAB/MeVisLab segmentation and quantification pipeline) publicly available on GitHub, and hosts supplementary materials on PNAS.Dataset · publicThe data in this study is available at https://doi.org/10.5281/zenodo.5650962 .Open asset ↗zenodo · 10.5281/zenodo.5650962lines:90-123Code · publicImage processing methods were programmed using MATLAB using the Image Processing Toolbox (MathWorks). Segmentation and extraction of geometrical features were performed using MeVisLab (MeVis Medical Solutions AG). All software is freely available from https://github.com/LionelDupuy/SENSOIL .Open asset ↗github · LionelDupuy/SENSOILlines:80-89Code / dataset availability confirmedCrossref · Europe PMC · OpenAlex · checked 9 Sept 2026
Abstract Background Being able to accurately assess the 3D architecture of plant canopies can allow us to better estimate plant productivity and improve our understanding of underlying plant processes. This is especially true if we can monitor these traits across plant development. Photogrammetry techniques, such as structure from motion, have been shown to provide accurate 3D reconstructions of monocot crop species such as wheat and rice, yet there has been little success reconstructing crop species with smaller leaves and more complex branching architectures, such as chickpea. Results In this work, we developed a low-cost 3D scanner and used an open-source data processing pipeline to assess the 3D structure of individual chickpea plants. The imaging system we developed consists of a user programmable turntable and three cameras that automatically captures 120 images of each plant and offloads these to a computer for processing. The capture process takes 5–10 min for each plant and the majority of the reconstruction process on a Windows PC is automated. Plant height and total plant surface area were validated against “ground truth” measurements, producing R 2 > 0.99 and a mean absolute percentage error Conclusions Our results show that it is possible to use low-cost photogrammetry techniques to accurately reconstruct individual chickpea plants, a crop with a complex architecture consisting of many small leaves and a highly branching structure. We hope that our use of open-source software and low-cost hardware will encourage others to use this promising technique for more architecturally complex species.
Why it matches plant phenotyping methodsヒヨコマメ個体の3D形態を取得する低コスト撮像システムとオープンソース解析パイプラインを開発し、草丈・表面積を基準値で検証しており、フェノタイピング手法が中心である。
abstractIn this work, we developed a low-cost 3D scanner and used an open-source data processing pipeline to assess the 3D structure of individual chickpea plants.
Reproduction assets foundThe authors deposited the paper's 3D point clouds and meshed chickpea models in an open-access Zenodo repository (DOI 10.5281/zenodo.4018242). Processing scripts are only included as article additional files, and the source images are available only on request from the corresponding author.Dataset · publicThe dataset supporting the conclusions of this article (3D point clouds and meshed models) are available in an open-access Zenodo repository, https://doi.org/10.5281/zenodo.4018242 .Open asset ↗Zenodo · 10.5281/zenodo.4018242lines:149-193Code / dataset availability confirmedEurope PMC · checked 9 Sept 2026
Laboratory / benchtopRootMorphology / geometry measurementRoot system architecture
Roots are central to the function of natural and agricultural ecosystems by driving plant acquisition of soil resources and influencing the carbon cycle. Root characteristics like length, diameter and volume are critical to measure to understand plant and soil functions. RhizoVision Explorer is an open-source software designed to enable researchers interested in roots by providing an easy-to-use interface, fast image processing and reliable measurements. The default broken roots mode is intended for roots sampled from pots and soil cores, washed and typically scanned on a flatbed scanner, and provides measurements like length, diameter and volume. The optional whole root mode for complete root systems or root crowns provides additional measurements such as angles, root depth and convex hull. Both modes support providing measurements grouped by defined diameter ranges, the inclusion of multiple regions of interest and batch analysis. RhizoVision Explorer was successfully validated against ground truth data using a new copper wire image set. In comparison, the current reference software, the commercial WinRhizo™, drastically underestimated volume when wires of different diameters were in the same image. Additionally, measurements were compared with WinRhizo™ and IJ_Rhizo using a simulated root image set, showing general agreement in software measurements, except for root volume. Finally, scanned root image sets acquired in different labs for the crop, herbaceous and tree species were used to compare results from RhizoVision Explorer with WinRhizo™. The two software showed general agreement, except that WinRhizo™ substantially underestimated root volume relative to RhizoVision Explorer. In the current context of rapidly growing interest in root science, RhizoVision Explorer intends to become a reference software, improve the overall accuracy and replicability of root trait measurements and provide a foundation for collaborative improvement and reliable access to all.
Why it matches plant phenotyping methods根画像から長さ・直径・体積などの植物形質を抽出するオープンソースソフトウェアを開発し、グラウンドトゥルースおよび既存ソフトウェアとの比較検証を行っており、植物フェノタイピング手法が中心である。
abstractRhizoVision Explorer is an open-source software designed to enable researchers interested in roots by providing an easy-to-use interface, fast image processing and reliable measurements.
Reproduction assets foundThe paper's own phenotyping assets are all publicly available: the RhizoVision Explorer source code (GitHub) and Windows binaries (Zenodo 3747697), the copper wire validation image set (Zenodo 4677546), the scanned root image sets from maize, wheat, herbaceous and tree species (Zenodo 4677751), and the R statistical/分析Code · publicThe open-source code for RhizoVision Explorer written in C++ is available at https://github.com/noble-research-institute/RhizoVisionExplorer on GitHub.Open asset ↗https://github.com/noble-research-institute/RhizoVisionExplorerlines:300-393Dataset · publicThe copper wire image set used here is available in a public repository and can be downloaded at http://doi.org/10.5281/zenodo.4677546 ( Dhakal et al. 2021a ).Open asset ↗zenodo · 10.5281/zenodo.4677546lines:86-101Dataset · publicThese four image sets of roots from several plant species are available in a public repository and can be downloaded at http://doi.org/10.5281/zenodo.4677751 ( Dhakal et al. 2021b ).Open asset ↗zenodo · 10.5281/zenodo.4677751lines:105-118Code / dataset availability confirmedOpenAlex · Europe PMC · checked 8 Sept 2026
The stomatal index of the leaf is the ratio of the number of stomata to the total number of stomata and epidermal cells. Comparing with the stomatal density, the stomatal index is relatively constant in environmental conditions and the age of the leaf and, therefore, of diagnostic characteristics for a given genotype or species. Traditional assessment methods involve manual counting of the number of stomata and epidermal cells in microphotographs, which is labor-intensive and time-consuming. Although several automatic measurement algorithms of stomatal density have been proposed, no stomatal index pipelines are currently available. The main aim of this research is to develop an automated stomatal index measurement pipeline. The proposed method employed Faster regions with convolutional neural networks (R-CNN) and U-Net and image-processing techniques to count stomata and epidermal cells, and subsequently calculate the stomatal index. To improve the labeling speed, a semi-automatic strategy was employed for epidermal cell annotation in each micrograph. Benchmarking the pipeline on 1,000 microscopic images of leaf epidermis in the wheat dataset (Triticum aestivum L.), the average counting accuracies of 98.03 and 95.03% for stomata and epidermal cells, respectively, and the final measurement accuracy of the stomatal index of 95.35% was achieved. R2 values between automatic and manual measurement of stomata, epidermal cells, and stomatal index were 0.995, 0.983, and 0.895, respectively. The average running time (ART) for the entire pipeline could be as short as 0.32 s per microphotograph. The proposed pipeline also achieved a good transferability on the other families of the plant using transfer learning, with the mean counting accuracies of 94.36 and 91.13% for stomata and epidermal cells and the stomatal index accuracy of 89.38% in seven families of the plant. The pipeline is an automatic, rapid, and accurate tool for the stomatal index measurement, enabling high-throughput phenotyping, and facilitating further understanding of the stomatal and epidermal development for the plant physiology community. To the best of our knowledge, this is the first deep learning-based microphotograph analysis pipeline for stomatal index assessment.
Why it matches plant phenotyping methods葉の顕微鏡画像から気孔と表皮細胞を検出・計数し、気孔指数を自動推定する画像解析パイプラインの開発とベンチマーク検証が研究の中心である。
abstractThe main aim of this research is to develop an automated stomatal index measurement pipeline.
Reproduction assets foundThe authors explicitly state the stomatal index pipeline code is fully open-source on GitHub and the wheat microscopic image dataset is downloadable as a zip release from the same repository. Both are paper-specific, public, and directly actionable.Code · publicThe code is fully open-source for academic usage and can be downloaded at https://github.com/WeizhenLiuBioinform/stomatal_indexOpen asset ↗WeizhenLiuBioinform/stomatal_indexlines:361-376Dataset · publicThe wheat dataset is available for downloading at https://github.com/WeizhenLiuBioinform/stomatal_index/releases/download/wheat1.0/wheat_dataset.zipOpen asset ↗WeizhenLiuBioinform/stomatal_index · wheat1.0lines:361-376Supplement · publicSupplementary Table 2
Description of the cuticle dataset used for training and testing the stomatal index measurement model.Open asset ↗lines:651-703Code / dataset availability confirmedarXiv · checked 13 Sept 2026
Obtaining 3D sensor data of complete plants or plant parts (e.g., the crop or fruit) is difficult due to their complex structure and a high degree of occlusion. However, especially for the estimation of the position and size of fruits, it is necessary to avoid occlusions as much as possible and acquire sensor information of the relevant parts. Global viewpoint planners exist that suggest a series of viewpoints to cover the regions of interest up to a certain degree, but they usually prioritize global coverage and do not emphasize the avoidance of local occlusions. On the other hand, there are approaches that aim at avoiding local occlusions, but they cannot be used in larger environments since they only reach a local maximum of coverage. In this paper, we therefore propose to combine a local, gradient-based method with global viewpoint planning to enable local occlusion avoidance while still being able to cover large areas. Our simulated experiments with a robotic arm equipped with a camera array as well as an RGB-D camera show that this combination leads to a significantly increased coverage of the regions of interest compared to just applying global coverage planning.
Why it matches plant phenotyping methods果実の位置・サイズ推定に必要な3Dセンサデータ取得を対象に、局所遮蔽回避と大域的視点計画を組み合わせる視点計画法を開発・評価しており、植物表現型取得が中心である。
abstractespecially for the estimation of the position and size of fruits, it is necessary to avoid occlusions as much as possible and acquire sensor information of the relevant parts
Reproduction assets foundThe paper's authors explicitly state that the source code of their combined local/global viewpoint planning system (used for fruit ROI coverage experiments) is publicly available on GitHub. OctoMap is a generic third-party library and is excluded.Code · publicThe source code of our system is available on GitHub 1 1
1
https://github.com/Eruvae/roi_viewpoint_planner .Open asset ↗Eruvae/roi_viewpoint_plannerlines:1-105Code / dataset availability confirmedCrossref · checked 14 Sept 2026
Nitrogen is an essential nutrient element required for optimum crop growth and yield. If a specific amount of nitrogen is not applied to crops, their yield is affected. Estimation of nitrogen level in crops is momentous to decide the nitrogen fertilization in crops. The amount of nitrogen in crops is measured through different techniques, including visual inspection of leaf color and texture and by laboratory analysis of plant leaves. Laboratory analysis-based techniques are more accurate than visual inspection, but they are costly, time-consuming, and require skilled laboratorian and precise equipment. Therefore, computer-based systems are required to estimate the amount of nitrogen in field crops. In this paper, a computer vision-based solution is introduced to solve this problem as well as to help farmers by providing an easier, cheaper, and faster approach for measuring nitrogen deficiency in crops. The system takes an image of the crop leaf as input and estimates the amount of nitrogen in it. The image is captured by placing the leaf on a specially designed slate that contains the reference green and yellow colors for that crop. The proposed algorithm automatically extracts the leaf from the image and computes its color similarity with the reference colors. In particular, we define a green color value (GCV) index from this analysis, which serves as a nitrogen indicator. We also present an evaluation of different color distance models to find a model able to accurately capture the color differences. The performance of the proposed system is evaluated on a Spinacia oleracea dataset. The results of the proposed system and laboratory analysis are highly correlated, which shows the effectiveness of the proposed system.
Why it matches plant phenotyping methods葉画像から窒素状態を推定するコンピュータビジョン手法の開発・評価が中心であり、植物生理状態の表現型取得法に該当する。
abstractIn this paper, a computer vision-based solution is introduced to solve this problem as well as to help farmers by providing an easier, cheaper, and faster approach for measuring nitrogen deficiency in crops.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicA software release of the proposed
vision-based framework for N-nutrient estimation in crops is made publicly available on
the project website: http://faculty.pucit.edu.pk/~farid/Research/GCV.html, accessed on
8 June 2021.Open asset ↗pdf-page:16 lines:1-55Code / dataset availability confirmedEurope PMC · checked 9 Sept 2026
Background Hyperaccumulation of trace elements is a rare trait among plants which is being investigated to advance our understanding of the regulation of metal accumulation and applications in phytotechnologies. Noccaea caerulescens (Brassicaceae) is an intensively studied hyperaccumulator model plant capable of attaining extremely high tissue concentrations of zinc and nickel with substantial genetic variation at the population-level. Micro-X-ray Fluorescence spectroscopy (µXRF) mapping is a sensitive high-resolution technique to obtain information of the spatial distribution of the plant metallome in hydrated samples. We used laboratory-based µXRF to characterize a collection of 86 genetically diverse Noccaea caerulescens accessions from across Europe. We developed an image-processing method to segment different plant substructures in the µXRF images. We introduced the concentration quotient (CQ) to quantify spatial patterns of metal accumulation and linked that to genetic variation. Results Image processing resulted in automated segmentation of µXRF plant images into petiole, leaf margin, leaf interveinal and leaf vasculature substructures. The harmonic means of recall and precision (F1 score) were 0.79, 0.80, 0.67, and 0.68, respectively. Spatial metal accumulation as determined by CQ is highly heritable in Noccaea caerulescens for all substructures, with broad-sense heritability (H 2 ) ranging from 76 to 92%, and correlates only weakly with other heritable traits. Insertion of noise into the image segmentation algorithm barely decreases heritability scores of CQ for the segmented substructures, illustrating the robustness of the trait and the quantification method. Very low heritability was found for CQ if randomly generated substructures were compared, validating the approach. Conclusions A strategy for segmenting µXRF images of Noccaea caerulescens is proposed and the concentration quotient is developed to provide a quantitative measure of metal accumulation pattern, which can be used to determine genetic variation for such pattern. The metric is robust to segmentation error and provides reliable H 2 estimates. This strategy provides an avenue for quantifying XRF data for analysis of the genetics of metal distribution patterns in plants and the subsequent discovery of new genes that regulate metal homeostasis and sequestration in plants.
Why it matches plant phenotyping methodsµXRF画像の植物組織分割と、金属蓄積空間パターンを定量化する指標を開発・検証しており、植物表現型の取得・抽出手法が中心である。
abstractWe developed an image-processing method to segment different plant substructures in the µXRF images.
Reproduction assets foundThe authors explicitly state that the analysis code created for this study (µXRF image segmentation and CQ/heritability analysis) is publicly available in their GitHub repository. The phenotype datasets themselves are only available on request from the corresponding author, so they are noted as a request-only asset. NoCode · publicCode is available at https://github.com/LucasYEAST/noccaea .Open asset ↗LucasYEAST/noccaealines:211-272Code / dataset availability confirmedEurope PMC · Crossref · checked 9 Sept 2026
Cassava brown streak disease (CBSD) is an emerging viral disease that can greatly reduce cassava productivity, while causing only mild aerial symptoms that develop late in infection. Early detection of CBSD enables better crop management and intervention. Current techniques require laboratory equipment and are labour intensive and often inaccurate. We have developed a handheld active multispectral imaging (A-MSI) device combined with machine learning for early detection of CBSD in real-time. The principal benefits of A-MSI over passive MSI and conventional camera systems are improved spectral signal-to-noise ratio and temporal repeatability. Information fusion techniques further combine spectral and spatial information to reliably identify features that distinguish healthy cassava from plants with CBSD as early as 28 days post inoculation. Application of the device has the potential to increase farmers' access to healthy planting materials and reduce losses due to CBSD in Africa. It can also be adapted for sensing other biotic and abiotic stresses in real-world situations where plants are exposed to multiple pest, pathogen and environmental stresses.
Why it matches plant phenotyping methods携帯型マルチスペクトル撮像装置と機械学習を開発し、カンショのウイルス感染状態を植物画像から早期推定する方法が中心である。
abstractWe have developed a handheld active multispectral imaging (A-MSI) device combined with machine learning for early detection of CBSD in real-time.
Reproduction assets foundThe paper's Data Availability section states the multispectral imaging dataset from the three Cassava-TME204-UCBSV trials is publicly deposited on Zenodo, matching the allowed URL exactly.Dataset · publicThe MSI dataset of these three trials (Cassava-TME204-UCBSV) are available at https://doi.org/10.5281/zenodo.4636968Open asset ↗zenodo · 10.5281/zenodo.4636968pdf-page:14 lines:1-50Code / dataset availability confirmedCrossref · Europe PMC · checked 15 Sept 2026
Recent technical advances in the computer-vision domain have facilitated the development of various methods for achieving image-based quantification of stomata-related traits. However, the installation cost of such a system and the difficulties of operating it on-site have been hurdles for experimental biologists. Here, we present a platform that allows real-time stomata detection during microscopic observation. The proposed system consists of a deep neural network model-based stomata detector and an upright microscope connected to a USB camera and a graphics processing unit (GPU)-supported single-board computer. All the hardware components are commercially available at common electronic commerce stores at a reasonable price. Moreover, the machine-learning model is prepared based on freely available cloud services. This approach allows users to set up a phenotyping platform at low cost. As a proof of concept, we trained our model to detect dumbbell-shaped stomata from wheat leaf imprints. Using this platform, we collected a comprehensive range of stomatal phenotypes from wheat leaves. We confirmed notable differences in stomatal density ( SD ) between adaxial and abaxial surfaces and in stomatal size ( SS ) between wheat-related species of different ploidy. Utilizing such a platform is expected to accelerate research that involves all aspects of stomata phenotyping.
Why it matches plant phenotyping methods低コストの顕微鏡画像と深層学習による気孔検出・形質定量化プラットフォームの開発であり、植物フェノタイピング手法が研究の中心です。
abstractHere, we present a platform that allows real-time stomata detection during microscopic observation.
Reproduction assets foundThe paper's stomata-detection GUI, trained SSD model weights, and model-training workflow are publicly available in the authors' GitHub repository (onsite_stomata_platform) with an executable Colab training notebook. The raw phenotype/image datasets are only available on request per the Data Availability Statement.Code · publicDetailed codes and instructions to reproduce the regarding system as well as the stomata detection model is described in Google Colaboratory executable notebook 7 hosted at https://github.com/totti0223/onsite_stomata_platform .Open asset ↗totti0223/onsite_stomata_platformlines:155-166Code / dataset availability confirmedCrossref · checked 9 Sept 2026
Laboratory / benchtopChlorophyll fluorescenceMicroscopyRootGrowth / time-series analysisVisualization / data management
Fabricated ecosystems (EcoFABs) offer an innovative approach to in situ examination of microbial establishment patterns around plant roots using nondestructive, high-resolution microscopy. Previously high-resolution imaging was challenging because the roots were not constrained to a fixed distance from the objective. Here, we describe a new ‘Imaging EcoFAB’ and the use of this device to image the entire root system of growing Brachypodium distachyon at high resolutions (20×, 40×) over a 3-week period. The device is capable of investigating root–microbe interactions of multimember communities. We examined nine strains of Pseudomonas simiae with different fluorescent constructs to B. distachyon and individual cells on root hairs were visible. Succession in the rhizosphere using two different strains of P. simiae was examined, where the second addition was shown to be able to establish in the root tissue. The device was suitable for imaging with different solid media at high magnification, allowing for the imaging of fungal establishment in the rhizosphere. Overall, the Imaging EcoFAB could improve our ability to investigate the spatiotemporal dynamics of the rhizosphere, including studies of fluorescently-tagged, multimember, synthetic communities.
Why it matches plant phenotyping methods植物根系全体を高解像度・経時的に撮像するための新規チャンバーを開発し、その撮像性能と用途を示しており、表現型取得法が研究の中心である。
abstractHere, we describe a new ‘Imaging EcoFAB’ and the use of this device to image the entire root system of growing Brachypodium distachyon at high resolutions (20×, 40×) over a 3-week period.
Reproduction assets foundThe paper's computational analysis (K-means clustering and segmentation/cell counting of the 40× multispectral root image) is explicitly stated to have its environment, code, and parent data file available in the Supplementary Materials, hosted at the MDPI S1 link. Additionally, the 3D-printing-ready Imaging EcoFAB 3D-Code · publicThe environment, code, and parent data file are available in the Supplementary Materials .Open asset ↗lines:65-81Code / dataset availability confirmedbioRxiv · Europe PMC · checked 15 Sept 2026
Plants respond to the surrounding environment in countless ways. One of these responses is their ability to sense and orient their root growth toward the gravity vector. Root gravitropism is studied in many laboratories as a hallmark of auxin-related phenotypes. However, manual analysis of images and microscopy data is known to be subjected to human bias. This is particularly the case for manual measurements of root bending as the selection lines to calculate the angle are set subjectively. Therefore, it is essential to develop and use automated or semi-automated image analysis to produce reproducible and unbiased data. Moreover, the increasing usage of vertical-stage microscopy in plant root biology yields gravitropic experiments with an unprecedented spatiotemporal resolution. To this day, there is no available solution to measure root bending angle over time for vertical-stage microscopy. To address these problems, we developed ACORBA (Automatic Calculation Of Root Bending Angles), a fully automated software to measure root bending angle over time from vertical-stage microscope and flatbed scanner images. Moreover, the software can be used semi-automated for camera, mobile phone or stereomicroscope images. ACORBA represents a flexible approach based on both traditional image processing and deep machine learning segmentation to measure root angle progression over time. By its automated nature, the workflow is limiting human interactions and has high reproducibility. ACORBA will support the plant biologist community by reducing time and labor and by producing quality results from various kinds of inputs. Significance statementACORBA is implementing an automated and semi-automated workflow to quantify root bending and waving angles from images acquired with a microscope, a scanner, a stereomicroscope or a camera. It will support the plant biology community by reducing time and labor and by producing trustworthy and reproducible quantitative data.
Why it matches plant phenotyping methods根の屈曲角度を画像から自動抽出するソフトウェアとワークフローの開発が研究の中心であり、植物形態表現型の定量手法に該当する。
abstractwe developed ACORBA (Automatic Calculation Of Root Bending Angles), a fully automated software to measure root bending angle over time from vertical-stage microscope and flatbed scanner images.
Reproduction assets foundThe paper explicitly releases the ACORBA software (source code, trained models, annotated training libraries, notebooks, user manual) on SourceForge and the raw microscopy/scanner image stacks used for the root-angle measurements on Zenodo (DOI 10.5281/zenodo.5105719). Both are paper-specific, public, and actionable.Code · publicand
online Python image analysis and machine learning tutorials.
Availability of data and materials
The latest versions of ACORBA software training annotated libraries, source code, examples,
image pre-processing scripts, deep machine learning model training Jupyter notebooks and user
manual maintained by NBCS are available at https://sourceforge.net/projects/acorba/. The raw
microscopy and scanner stacks used in this paper are available at ZENODO
(https://doi.org/10.5281/zenodo.5105719). The analyzed results are supplemented (Supplemental
data).
Competing interests
The authors declare that they have no competing interests.
Funding
This work was supported by the European Research Council (GOpen asset ↗sourceforge.net/projects/acorbapdf-raw-page:17 lines:1-45Dataset · publicACORBA software training annotated libraries, source code, examples,
image pre-processing scripts, deep machine learning model training Jupyter notebooks and user
manual maintained by NBCS are available at https://sourceforge.net/projects/acorba/. The raw
microscopy and scanner stacks used in this paper are available at ZENODO
(https://doi.org/10.5281/zenodo.5105719). The analyzed results are supplemented (Supplemental
data).
Competing interests
The authors declare that they have no competing interests.
Funding
This work was supported by the European Research Council (Grant No. 803048), Charles
University Primus (Grant No. PRIMUS/19/SCI/09).
Author contributions
NBCS and MF conceived the pOpen asset ↗ZENODO · 10.5281/zenodo.5105719pdf-raw-page:17 lines:1-45Code / dataset availability confirmedOpenAlex · Crossref · Europe PMC · checked 8 Sept 2026
Laboratory / benchtopRoot2D/3D reconstructionSegmentationGrowth / time-series analysisGrowth / development / phenologyRoot system architecture
BACKGROUND: Deep learning methods have outperformed previous techniques in most computer vision tasks, including image-based plant phenotyping. However, massive data collection of root traits and the development of associated artificial intelligence approaches have been hampered by the inaccessibility of the rhizosphere. Here we present ChronoRoot, a system that combines 3D-printed open-hardware with deep segmentation networks for high temporal resolution phenotyping of plant roots in agarized medium. RESULTS: We developed a novel deep learning-based root extraction method that leverages the latest advances in convolutional neural networks for image segmentation and incorporates temporal consistency into the root system architecture reconstruction process. Automatic extraction of phenotypic parameters from sequences of images allowed a comprehensive characterization of the root system growth dynamics. Furthermore, novel time-associated parameters emerged from the analysis of spectral features derived from temporal signals. CONCLUSIONS: Our work shows that the combination of machine intelligence methods and a 3D-printed device expands the possibilities of root high-throughput phenotyping for genetics and natural variation studies, as well as the screening of clock-related mutants, revealing novel root traits.
Why it matches plant phenotyping methods根系画像の深層セグメンテーションと3D装置を開発し、画像から根系形態・成長動態を自動抽出する方法が研究の中心である。
abstractHere we present ChronoRoot, a system that combines 3D-printed open-hardware with deep segmentation networks for high temporal resolution phenotyping of plant roots in agarized medium.
Reproduction assets foundThe paper publicly releases its root segmentation image/annotation datasets, hardware files, and analysis code via GitHub repositories, plus supporting data in GigaDB. Three qualifying paper-specific assets with allowed URLs are listed; the GigaDB deposit (10.5524/100911) is paper-specific but its URL is not in the允许edCode · publicThe source code corresponding to ChronoRoot imaging controller, namely, the web interface to check and set up the image acquisition parameters:
Project name: ChronoRoot: Module Controller
Project home page: https://github.com/ThomasBlein/ChronoRootControlOpen asset ↗https://github.com/ThomasBlein/ChronoRootControllines:185-222Dataset · publicThe 2 datasets of images and annotations described in the Datasets section, as well as the 3D printing and laser cutting files, are publicly available at https://github.com/ThomasBlein/ChronoRootModuleHardware under the CERN Open Hardware License Version 2—Strongly Reciprocal licence.Open asset ↗https://github.com/ThomasBlein/ChronoRootModuleHardwarelines:223-262Code / dataset availability confirmedEurope PMC · checked 9 Sept 2026
Urochloa (including Brachiaria , Megathyrus and some Panicum ) tropical grasses are native to Africa and are now, after selection and breeding, planted worldwide, particularly in South America, as important forages with huge potential for further sustainable improvement and conservation of grasslands. We aimed to develop an optimized approach to determine ploidy of germplasm collection of this tropical forage grass group using dried leaf material, including approaches to collect, dry and preserve plant samples for flow cytometry analysis. Our methods enable robust identification of ploidy levels (coefficient of variation of G0/G1 peaks, CV, typically x to 9 x ), from international genetic resource collections, showing variation in basic chromosome numbers and reproduction modes (apomixis and sexual), were determined using our defined standard protocol. Two major Urochloa agamic complexes are used in the current breeding programs at CIAT and EMBRAPA: the ' brizantha ' and ' humidicola ' agamic complexes are variable, with multiple ploidy levels. Some U. brizantha accessions have odd level of ploidy (5 x ), and the relative differences in fluorescence values of the peak positions between adjacent cytotypes is reduced, thus more precise examination of this species is required. Ploidy measurement of U. humidicola revealed aneuploidy.
Why it matches plant phenotyping methods乾燥葉を用いたフローサイトメトリーによる植物の倍数性測定法を最適化し、標準プロトコルとして確立することが研究の中心であるため、植物表現型測定法として採用する。
abstractWe aimed to develop an optimized approach to determine ploidy of germplasm collection of this tropical forage grass group using dried leaf material, including approaches to collect, dry and preserve plant samples for flow cytometry analysis.
Reproduction assets foundThe paper's Supplementary Data Table S1 (hosted at the MDPI supplementary URL) contains the paper-specific phenotype measurements: the list of 348 Urochloa accessions with their flow cytometry fluorescence peak positions and G0/G1 CVs. This is a public, directly actionable dataset reproducing the paper's ploidy/phenotyDataset · publicThe following are available online at https://www.mdpi.com/article/10.3390/genes12070957/s1 , Supplementary Data Table S1. List of accessions used in the study, their fluorescence values of the peak positions, and coefficient of variations (CVs) of the G0/G1 peaks.Open asset ↗lines:351-363Code / dataset availability confirmedOpenAlex · Europe PMC · bioRxiv · checked 8 Sept 2026
ABSTRACT Lack of high throughput phenotyping systems for determining moisture content during the maize nixtamalization cooking process has led to difficulty in breeding for this trait. This study provides a high throughput, quantitative measure of kernel moisture content during nixtamalization based on NIR scanning of uncooked maize kernels. Machine learning was utilized to develop models based on the combination of NIR spectra and moisture content determined from a scaled-down benchtop cook method. A linear support vector machine (SVM) model with a Spearman’s rank correlation coefficient of 0.852 between wet lab and predicted values was developed from 100 diverse temperate genotypes grown in replicate across two environments. This model was applied to NIR data from 501 diverse temperate genotypes grown in replicate in five environments. Analysis of variance revealed environment explained the highest percent of the variation (51.5%), followed by genotype (15.6%) and genotype-by-environment interaction (11.2%). A genome-wide association study identified 26 significant loci across five environments that explained between 5.04% and 16.01% (average = 10.41%). However, genome-wide markers explained 10.54% to 45.99% (average = 31.68%) of the variation, indicating the genetic architecture of this trait is likely complex and controlled by many loci of small effect. This study provides a high-throughput method to evaluate moisture content during nixtamalization that is feasible at the scale of a breeding program and provides important information about the factors contributing to variation of this trait for breeders and food companies to make future strategies to improve this important processing trait. Key Message Moisture content during nixtamalization can be accurately predicted from NIR spectroscopy when coupled with a support vector machine (SVM) model, is strongly modulated by the environment, and has a complex genetic architecture.
Why it matches plant phenotyping methodsNIRスペクトルとSVMを用いて、トウモロコシ種子の加工中水分含量を高スループットかつ定量的に推定する方法の開発・検証が研究の中心であり、育種規模への適用も示している。
abstractThis study provides a high throughput, quantitative measure of kernel moisture content during nixtamalization based on NIR scanning of uncooked maize kernels.
Reproduction assets foundThe paper's Code Availability section states all analysis code is publicly available on GitHub at the HirschLabUMN ML_Moisture_Prediction repository, which is an allowed URL. This is the authors' code for the NIR/machine-learning moisture prediction analysis. No separate public phenotype dataset deposit is explicitly aCode · publicCode Availability
All code is publicly available on GitHub at https://github.com/HirschLabUMN/ML_Moisture_Prediction.Open asset ↗HirschLabUMN/ML_Moisture_Predictionpdf-page:15 lines:1-55Code / dataset availability confirmedEurope PMC · bioRxiv · checked 9 Sept 2026
ABSTRACT Over 800 million people across the tropics rely on cassava as a major source of calories. While the root dry matter content (RDMC) of this starchy root crop is important for both producers and consumers, characterization of RDMC by traditional methods is time-consuming and laborious for breeding programs. Alternate phenotyping methods have been proposed but lack the accuracy, cost, or speed ultimately needed for cassava breeding programs. For this reason, we investigated the use of a low-cost, handheld NIR spectrometer for field-based RDMC prediction in cassava. Oven-dried measurements of RDMC were paired with 21,044 scans of roots of 376 diverse clones from 10 field trials in Nigeria and grouped into training and test sets based on cross-validation schemes relevant to plant breeding programs. Mean partial least squares regression model performance ranged from R 2 p = 0.62 - 0.89 for within-trial predictions, which is within the range achieved with laboratory-grade spectrometers in previous studies. Relative to other factors, model performance was highly impacted by the inclusion of samples from the same environment in both the training and test sets. Random forest variable importance analysis of root spectra revealed increased importance in a region previously identified as predictive of water content in plants (~950 - 990 nm). With appropriate model calibration, the tested spectrometer will allow for field-based collection of spectral data with a smartphone for accurate RDMC prediction and potentially other quality traits, a step that could be easily integrated into existing harvesting workflows of cassava breeding programs. CORE IDEAS A low-cost, handheld near-infrared spectrometer was tested for phenotyping of cassava roots Plant breeding-relevant cross-validation schemes were used for predictions High prediction accuracies were achieved for cassava root dry matter content A spectral region predictive of plant water content was identified as important
Why it matches plant phenotyping methodsカッサバ根の乾物含量という植物形質を対象に、低コスト携帯型NIR分光計と予測モデルを開発・検証しており、フェノタイピング手法が研究の中心である。
abstractwe investigated the use of a low-cost, handheld NIR spectrometer for field-based RDMC prediction in cassava.
Reproduction assets foundThe paper's raw RDMC and NIR spectral data (21,044 SCiO scans paired with oven-dry RDMC from 10 Nigerian field trials) are publicly deposited on Cyverse under the GoreLab shared directory, as stated in the Data Availability section. The analysis R code on GitHub (GoreLab/CassavaNIRS) is paper-specific but its URL is anDataset · publicRaw RDMC and spectral data are available for download on Cyverse atOpen asset ↗Cyversepdf-page:20 lines:1-54Code / dataset availability confirmedEurope PMC · Crossref · checked 9 Sept 2026
Abstract Identification of plant disease is usually done through visual inspection or during laboratory examination which causes delays resulting in yield loss by the time identification is complete. On the other hand, complex deep learning models perform the task with reasonable performance but due to their large size and high computational requirements, they are not suited to mobile and handheld devices. Our proposed approach contributes automated identification of plant diseases which follows a sequence of steps involving pre-processing, segmentation of diseased leaf area, calculation of features based on the Gray-Level Co-occurrence Matrix (GLCM), feature selection and classification. In this study, six color features and twenty-two texture features have been calculated. Support vector machines is used to perform one-vs-one classification of plant disease. The proposed model of disease identification provides an accuracy of 98.79% with a standard deviation of 0.57 on 10-fold cross-validation. The accuracy on a self-collected dataset is 82.47% for disease identification and 91.40% for healthy and diseased classification. The reported performance measures are better or comparable to the existing approaches and highest among the feature-based methods, presenting it as the most suitable method to automated leaf-based plant disease identification. This prototype system can be extended by adding more disease categories or targeting specific crop or disease categories.
Why it matches plant phenotyping methods葉画像から病変部位を抽出し、色・テクスチャ特徴量と分類器で植物病害状態を推定する手法の開発・検証が中心であり、植物フェノタイピング手法に該当する。
abstractOur proposed approach contributes automated identification of plant diseases which follows a sequence of steps involving pre-processing, segmentation of diseased leaf area, calculation of features based on the Gray-Level Co-occurrence Matrix (GLCM), feature selection and classification.
Reproduction assets foundThe paper's experiments use the public PlantVillage leaf image dataset (54,309 images, 38 classes), which the authors explicitly state is available at the given GitHub URL. The authors' analysis code is only promised after acceptance, so it is not a qualifying public asset.Dataset · publicAvailability of data and material: The data used for experiments is available at
https://github.com/spMohanty/PlantVillage-DatasetOpen asset ↗spMohanty/PlantVillage-Datasetpdf-page:20 lines:1-46Code / dataset availability confirmedEurope PMC · bioRxiv · checked 9 Sept 2026
Laboratory / benchtopRootMorphology / geometry measurementSegmentationRoot system architecture
Roots are central to the function of natural and agricultural ecosystems by driving plant acquisition of soil resources and influencing the carbon cycle. Root characteristics like length, diameter, and volume are critical to measure to understand plant and soil functions. RhizoVision Explorer is an open-source software designed to enable researchers interested in roots by providing an easy-to-use interface, fast image processing, and reliable measurements. The default broken roots mode is intended for roots sampled from pots or soil cores, washed, and typically scanned on a flatbed scanner, and provides measurements like length, diameter, and volume. The optional whole root mode for complete root systems or root crowns provides additional measurements such as angles, root depth, and convex hull. Both modes support providing measurements grouped by defined diameter ranges, the inclusion of multiple regions of interest, and batch analysis. RhizoVision Explorer was successfully validated against ground truth data using a novel copper wire image set. In comparison, the current reference software, the commercial WinRhizo™, drastically underestimated volume when wires of different diameters were in the same image. Additionally, measurements were compared with WinRhizo™ and IJ_Rhizo using a simulated root image set, showing general agreement in software measurements, except for root volume. Finally, scanned root image sets acquired in different labs for the crop, herbaceous, and tree species were used to compare results from RhizoVision Explorer with WinRhizo™. The two software showed general agreement, except that WinRhizo™ substantially underestimated root volume relative to RhizoVision Explorer. In the current context of rapidly growing interest in root science, RhizoVision Explorer intends to become a reference software, improve the overall accuracy and replicability of root trait measurements, and provide a foundation for collaborative improvement and reliable access to all. Abstract Figure
Why it matches plant phenotyping methods根画像から長さ・直径・体積などの植物形質を抽出するオープンソースソフトウェアの開発と、基準データおよび既存ソフトウェアとの技術検証が中心である。
abstractRhizoVision Explorer is an open-source software designed to enable researchers interested in roots by providing an easy-to-use interface, fast image processing, and reliable measurements.
Reproduction assets foundThe paper's copper wire validation image set is publicly deposited on Zenodo, and the authors' software binaries (Zenodo) and cvutil code library (GitHub) are explicitly released with public URLs. The simulated root image set (Zenodo 1159845) is cited prior work (Rose and Lobet 2018), not a paper-specific asset, and isDataset · publicThe copper wire image set used here is available in a public repository
and can be downloaded at http://doi.org/10.5281/zenodo.4677546 (Dhakal et al. 2021a).Open asset ↗zenodo · 10.5281/zenodo.4677546pdf-page:12 lines:1-49Code / dataset availability confirmedEurope PMC · checked 9 Sept 2026
Abstract Background Hyperaccumulation of trace elements is a rare trait among plants which is being investigated to advance our understanding of the regulation of metal accumulation and applications in phytotechnologies. Noccaea caerulescens (Brassicaceae) is an intensively studied hyperaccumulator model plant capable of attaining extremely high tissue concentrations of zinc, and nickel with substantial genetic variation at the population-level. X-ray Fluorescence microscopy (µXRF) is a sensitive high-resolution technique to obtain information of the spatial distribution of the plant metallome in hydrated samples We used laboratory-based µXRF to characterize a collection of 86 genetically diverse Noccaea caerulescens accessions from across Europe. We developed an image-processing method to segment different plant substructures in the µXRF images. We introduced the concentration quotient (CQ) to quantify spatial patterns of metal accumulation and linked that to genetic variation. Results Image processing resulted in automated segmentation of µXRF plant images into petiole, leaf margin, leaf interveinal and leaf vasculature substructures. The harmonic means of recall and precision (F1 score) were 0.79, 0.80, 0.67, and 0.68, respectively. Spatial metal accumulation as determined by CQ is highly heritable in Noccaea caerulescens for all substructures, with broad sense heritabilities (H 2 ) ranging from 76–92% correlates only weakly with other heritable traits. Insertion of noise into the image segmentation algorithm barely decreases heritability scores of CQ for the segmented substructures, illustrating the robustness of the trait and the quantification method. Very low heritability was found for CQ if randomly generated substructures were compared, validating the approach. Conclusions A strategy for segmenting µXRF images of Noccaea caerulescens is proposed and the concentration quotient is developed to provide a quantitative measure of metal accumulation pattern, which can be used to determine genetic variation for such pattern. The metric is robust to segmentation error and provides reliable H 2 estimates. This strategy provides an avenue for quantifying XRF data for analysis of the genetics of metal distribution patterns in plants and the subsequent discovery of new genes that regulate metal homeostasis and sequestration in plants.
Why it matches plant phenotyping methodsµXRF画像から植物器官を自動分割し、金属蓄積パターンを定量する画像処理法と指標を開発・検証しており、植物フェノタイピング手法が研究の中心である。
abstractWe developed an image-processing method to segment different plant substructures in the µXRF images.
Reproduction assets foundThe authors' image-processing/heritability analysis code for the µXRF plant phenotyping is explicitly deposited in a public GitHub repository. The phenotype datasets themselves are only available on request, and GeoPIXE is a generic third-party tool, not a paper-specific asset.Code · publicCode is
available at https://github.com/LucasYEAST/noccaea.Open asset ↗LucasYEAST/noccaeapdf-page:29 lines:1-48Code / dataset availability confirmedCrossref · checked 9 Sept 2026
Brassica oleracea is an important crop species that at early growth stages may exhibit failure of the apical growing point, an abnormality called “blindness”. The occurrence of blindness is promoted by exposure to low temperatures during imbibition and germination, but the causes of sensitivity to such conditions are unknown. We combined three analytical seed technology instruments to explore seed physical properties that are highly correlated with quality parameters and might be used directly for grading or sorting seed lots into subpopulations varying in potential susceptibility to blindness. For image analysis, we used the VideometerLab instrument, which can scan 19 wavelengths from ultraviolet to infrared and utilize that information in any combination to potentially identify unique criteria related to seed quality. The iXeed CF Analyzer was utilized to obtain chlorophyll fluorescence values for individual seeds. Chlorophyll contents of many seeds can be used as an indicator of seed maturity, a major contributor to seed quality. Finally, oxygen consumption measurements of individual seeds as obtained with the Q2 instrument are highly correlated with their performance under a wide variety of conditions. Six Brassica seed lots differed in their susceptibility to induction of blindness or loss of viability due to 48 h hydrated incubation at 1.5 ∘C. Analysis of physical and respiratory parameters identified some measurements that were highly correlated with the occurrence of blindness. Higher chlorophyll content, as detected by the CF-Mobile and certain wavelengths in the Videometer, was associated with greater occurrence of blindness or death following the induction treatment, suggesting that more immature seeds may be susceptible to blindness. Further research is required, but methods to detect and sort such seeds based on physical characteristics appear to be feasible.
Why it matches plant phenotyping methods種子の画像・蛍光・呼吸測定を組み合わせ、物理特性から発芽品質やblindness感受性を評価・選別する方法が研究の中心であり、単なる生物学的結果測定ではない。
abstractWe combined three analytical seed technology instruments to explore seed physical properties that are highly correlated with quality parameters and might be used directly for grading or sorting seed lots into subpopulations varying in potential susceptibility to blindness.
Reproduction assets foundThe paper's individual-seed phenotyping measurements (chlorophyll fluorescence, multispectral imaging, Q2 respiration, plant blindness scores) are consolidated in Supplemental Table S1 (Seed parameters database) and related supplements, publicly hosted on the MDPI article site. No author analysis code was deposited; CRDataset · publicSupplementary Materials: The following are available at https://www.mdpi.com/2077-0472/11/3
/220/s1, Table S1: Seed parameters database, Table S2: Q2 parameters, Table S3: MFA EigenvaluesOpen asset ↗pdf-page:20 lines:1-58Code / dataset availability confirmedEurope PMC · Crossref · checked 15 Sept 2026
Tissue clearing methods combined with confocal microscopy have been widely used for studying developmental biology. In plants, ClearSee is a reliable clearing method that is applicable to a wide range of tissues and is suitable for gene expression analysis using fluorescent reporters, but its application to the Arabidopsis thaliana embryo, a model system to study morphogenesis and pattern formation, has not been described in the original literature. Here, we describe a ClearSee-based clearing protocol which is suitable for obtaining 3D images of Arabidopsis thaliana embryos. The method consists of embryo dissection, fixation, washing, clearing, and cell wall staining and enables high-quality 3D imaging of embryo morphology and expression of fluorescent reporters with the cellular resolution. Our protocol provides a reliable method that is applicable to the analysis of morphogenesis and gene expression patterns in Arabidopsis thaliana embryos.
Why it matches plant phenotyping methodsArabidopsis胚の形態を細胞解像度で3D取得するClearSeeベースのクリアリング・画像化プロトコルが研究の中心であり、植物表現型の取得方法を開発している。
abstractHere, we describe a ClearSee-based clearing protocol which is suitable for obtaining 3D images of Arabidopsis thaliana embryos.
Reproduction assets foundThe paper's supplementary materials include Movie S1, the Z-stack confocal image data (157 serial optical sections) used for the paper's 3D embryo visualization analysis, publicly available at the MDPI supplementary URL. No author analysis code or trained models are reported.Supplement · publicThe following are available online at https://www.mdpi.com/2223-7747/10/2/190/s1 , Movie S1: Z-stack images of 157 serial optical sections used for Figure 2 ; Table S1: Primers used in this study.
Click here for additional data file.
Author Contributions
Conceptualization, M.A.; methodology, M.A.; validation, A.I. and M.A.; formal analysis, A.I.; investigation, A.I., M.Y., T.S., A.O., and M.A.; resources, TOpen asset ↗lines:58-85Code / dataset availability confirmedEurope PMC · checked 9 Sept 2026
Image-based symptom scoring of plant diseases is a powerful tool for associating disease resistance with plant genotypes. Advancements in technology have enabled new imaging and image processing strategies for statistical analysis of time-course experiments. There are several tools available for analyzing symptoms on leaves and fruits of crop plants, but only a few are available for the model plant Arabidopsis thaliana (Arabidopsis). Arabidopsis and the model fungus Botrytis cinerea (Botrytis) comprise a potent model pathosystem for the identification of signaling pathways conferring immunity against this broad host-range necrotrophic fungus. Here, we present two strategies to assess severity and symptom progression of Botrytis infection over time in Arabidopsis leaves. Thus, a pixel classification strategy using color hue values from red-green-blue (RGB) images and a random forest algorithm was used to establish necrotic, chlorotic, and healthy leaf areas. Secondly, using chlorophyll fluorescence (ChlFl) imaging, the maximum quantum yield of photosystem II (F v /F m ) was determined to define diseased areas and their proportion per total leaf area. Both RGB and ChlFl imaging strategies were employed to track disease progression over time. This has provided a robust and sensitive method for detecting sensitive or resistant genetic backgrounds. A full methodological workflow, from plant culture to data analysis, is described.
Why it matches plant phenotyping methods植物病害の症状・重症度・進展を画像から定量化する方法の開発とワークフロー提示が中心であり、植物状態の表現型取得に該当する。
abstractHere, we present two strategies to assess severity and symptom progression of Botrytis infection over time in Arabidopsis leaves.
Reproduction assets foundThe authors explicitly state that all R and ImageJ scripts and the study data are openly available in their public GitHub repository, which directly reproduces this paper's Botrytis symptom phenotyping analysis.Code · publicAll R and ImageJ script generated to process are available at https://github.com/mipavici/MDPI_leaf_infection .Open asset ↗mipavici/MDPI_leaf_infectionlines:69-123Dataset · publicThe data presented in this study are openly available at https://github.com/mipavici/MDPI_leaf_infection .Open asset ↗mipavici/MDPI_leaf_infectionlines:69-123Code / dataset availability confirmedOpenAlex · Europe PMC · checked 8 Sept 2026
ArabidopsisLaboratory / benchtopSeed / grainObject detectionGrowth / development / phenology
A high throughput phenotyping tool for seed germination, the ScreenSeed technology, was developed with the aim of screening genotype responsiveness and chemical drugs. This technology was presently used with Arabidopsis thaliana seeds to allow characterizing seed samples germination behavior by incubating seeds in 96-well microplates under defined conditions and detecting radicle protrusion through the seed coat by automated image analysis. This study shows that this technology provides a fast procedure allowing to handle thousands of seeds without compromising repeatability or accuracy of the germination measurements. Potential biases of the experimental protocol were assessed through statistical analyses of germination kinetics. Comparison of the ScreenSeed procedure with commonly used germination tests based upon visual scoring displayed very similar germination kinetics.
Why it matches plant phenotyping methods種子発芽を自動画像解析で測定する高スループット表現型解析法を開発し、再現性・精度・既存法との一致を検証しており、測定手法自体が中心である。
abstractA high throughput phenotyping tool for seed germination, the ScreenSeed technology, was developed
Reproduction assets foundThe paper's seed-by-seed germination time measurements (the core phenotyping data) are published as online supplementary XLSX files (Supplementary Data S3, S4, S5), and a ZIP supplement (Supplementary Information 2) corresponds to the image time series (Supplementary Data S2). These are hosted with the open-access (CC Dataset · publicAll the germination time seed by seed in the analyses are provided in the Supplementary Data S3 online for Col-0 accession in water condition, in Supplementary Data S4 online for comparison with standard assays and in Supplementary Data S5 online for the analyse of Col-0 and L er ABA dose response.Open asset ↗lines:101-105Code / dataset availability confirmedOpenAlex · Europe PMC · Crossref · checked 14 Sept 2026
Nutrient uptake is critical for crop growth and is determined by root foraging in soil. Growth and branching of roots lead to effective root placement to acquire nutrients, but relatively little is known about absorption of nutrients at the root surface from the soil solution. This knowledge gap could be alleviated by understanding sources of genetic variation for short-term nutrient uptake on a root length basis. A modular platform called RhizoFlux was developed for high-throughput phenotyping of multiple ion-uptake rates in maize (Zea mays L.). Using this system, uptake rates were characterized for the crop macronutrients nitrate, ammonium, potassium, phosphate, and sulfate among the Nested Association Mapping (NAM) population founder lines. The data revealed substantial genetic variation for multiple ion-uptake rates in maize. Interestingly, specific nutrient uptake rates (nutrient uptake rate per length of root) were found to be both heritable and distinct from total uptake and plant size. The specific uptake rates of each nutrient were positively correlated with one another and with specific root respiration (root respiration rate per length of root), indicating that uptake is governed by shared mechanisms. We selected maize lines with high and low specific uptake rates and performed an RNA-seq analysis, which identified key regulatory components involved in nutrient uptake. The high-throughput multiple ion-uptake kinetics pipeline will help further our understanding of nutrient uptake, parameterize holistic plant models, and identify breeding targets for crops with more efficient nutrient acquisition.
Why it matches plant phenotyping methods根の複数イオン吸収速度を高スループットで測定するRhizoFluxプラットフォームを開発し、性能・遺伝的変異を評価しており、植物表現型取得法が研究の中心です。
abstractA modular platform called RhizoFlux was developed for high-throughput phenotyping of multiple ion-uptake rates in maize (Zea mays L.).
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicthe statistical analysis R codes including the packages needed are available at https://doi.org/10.5281/zenodo.3893944 ( Griffiths and York, 2020b )Open asset ↗Zenodo · 10.5281/zenodo.3893944lines:83-89Code / dataset availability confirmedEurope PMC · checked 9 Sept 2026
Background Assessment of seed germination is an essential task for seed researchers to measure the quality and performance of seeds. Usually, seed assessments are done manually, which is a cumbersome, time consuming and error-prone process. Classical image analyses methods are not well suited for large-scale germination experiments, because they often rely on manual adjustments of color-based thresholds. We here propose a machine learning approach using modern artificial neural networks with region proposals for accurate seed germination detection and high-throughput seed germination experiments. Results We generated labeled imaging data of the germination process of more than 2400 seeds for three different crops, Zea mays (maize), Secale cereale (rye) and Pennisetum glaucum (pearl millet), with a total of more than 23,000 images. Different state-of-the-art convolutional neural network (CNN) architectures with region proposals have been trained using transfer learning to automatically identify seeds within petri dishes and to predict whether the seeds germinated or not. Our proposed models achieved a high mean average precision (mAP) on a hold-out test data set of approximately 97.9%, 94.2% and 94.3% for Zea mays, Secale cereale and Pennisetum glaucum respectively. Further, various single-value germination indices, such as Mean Germination Time and Germination Uncertainty, can be computed more accurately with the predictions of our proposed model compared to manual countings. Conclusion Our proposed machine learning-based method can help to speed up the assessment of seed germination experiments for different seed cultivars. It has lower error rates and a higher performance compared to conventional and manual methods, leading to more accurate germination indices and quality assessments of seeds.
Why it matches plant phenotyping methods種子の発芽状態を画像と機械学習で自動抽出し、手動計数と性能比較しているため、植物表現型取得法が中心です。
abstractWe here propose a machine learning approach using modern artificial neural networks with region proposals for accurate seed germination detection and high-throughput seed germination experiments.
Reproduction assets foundThe paper's authors publicly released the labeled germination image dataset (~24,000 annotated images of 2449 seeds) on Mendeley Data and their machine learning analysis code on GitHub, both explicitly stated in the Availability of data and materials section.Dataset · publicThe generated and labeled training data is freely available on Mendeley Data: http://dx.doi.org/10.17632/4wkt6thgp6.2 .Open asset ↗Mendeley Data · 10.17632/4wkt6thgp6.2lines:164-248Code · publicThe code for our proposed machine learning–based model can be found on GitHub: https://github.com/grimmlab/GerminationPrediction .Open asset ↗GitHub · grimmlab/GerminationPredictionlines:164-248Code / dataset availability confirmedEurope PMC · Crossref · bioRxiv · checked 15 Sept 2026
Capturing complete internal anatomies of plant organs and tissues within their relevant morphological context remains a key challenge in plant science. While plant growth and development are inherently multiscale, conventional light, fluorescence, and electron microscopy platforms are typically limited to imaging of plant microstructure from small flat samples that lack direct spatial context to, and represent only a small portion of, the relevant plant macrostructures. We demonstrate technical advances with a lab-based X-ray microscope (XRM) that bridge the imaging gap by providing multiscale high-resolution 3D volumes of intact plant samples from the cell to whole plant level. Serial imaging of a single sample is shown to provide sub-micron 3D volumes co-registered with lower magnification scans for explicit contextual reference. High quality 3D volume data from our enhanced methods facilitate more sophisticated and effective computational segmentation and analyses than have previously been employed for X-ray based imaging. Advances in sample preparation make multimodal correlative imaging workflows possible, where a single resin-embedded plant sample is scanned via XRM to generate a 3D cell-level map, and then used to identify and zoom in on sub-cellular regions of interest for high resolution scanning electron microscopy. In total, we present the methodologies for use of XRM in the multiscale and multimodal analysis of 3D plant features using numerous economically and scientifically important plant systems.
Why it matches plant phenotyping methods植物試料の細胞から個体までを対象に、X線顕微鏡によるマルチスケール3D画像取得、試料調製、計算セグメンテーション、相関イメージングの方法論を中心に提示しており、植物形態の取得・解析法が明確に中心です。
abstractWe demonstrate technical advances with a lab-based X-ray microscope (XRM) that bridge the imaging gap by providing multiscale high-resolution 3D volumes of intact plant samples from the cell to whole plant level.
Reproduction assets foundThe preprint points to a public figshare collection containing the paper's high-resolution XRM image stacks ('flythroughs') and videos of the 3D plant datasets, which directly reproduce the paper's phenotyping imaging measurements. No author analysis code or trained model checkpoint is explicitly deposited; the deep-seDataset · publicof these improved techniques will
112
make a significant contribution to plant biology, expanding the reach of XRM as a
113
routine tool for 3D imaging for plant scientists.
114
115
116
RESULTS1
117
118
Meristem Biology
119
1
high-resolution image stacks (“flythroughs”) and videos portraying the 3D data sets can be found here:
https://figshare.com/s/944efc8832e47fd4f203
.
CC-BY-NC 4.0 International license
available under a
(which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made
The copyright holder for this preprint
this version posted December 22, 2020.
;
https://doi.org/10.1101/2020.12.18.423480
doiOpen asset ↗figsharepdf-raw-page:4 lines:1-64Code / dataset availability confirmedbioRxiv · checked 15 Sept 2026
Root hydraulic properties play a central role in the global water cycle, agricultural systems productivity, and ecosystem survival as they impact the global canopy water supply. However, the available experimental methods to quantify root hydraulic conductivities, such as the root pressure probing, are particularly challenging and their applicability on thin roots and small root segments is limited. There is a gap in methods enabling easy estimations of root hydraulic conductivities across a diversity of root types and at high resolution along root axes. In this case study, we analysed Zea mays (maize) plants of the var. B73 that were grown in pots for 14 days. Root cross-section data were used to extract anatomical measurements. We used the Generator of Root Anatomy in R (GRANAR) model to generate root anatomical networks from anatomical features. Then we used the Model of Explicit Cross-section Hydraulic Anatomy (MECHA) to compute an estimation of the root axial and radial hydraulic conductivities (kx and kr, respectively), based on the generated anatomical networks and cell hydraulic properties from the literature. The root hydraulic conductivity maps obtained from the root cross-sections suggest significant functional variations along and between different root types. Predicted variations of kr along the root axis were strongly dependent on the maturation stage of hydrophobic barriers. The same was also true for the maturation rates of the metaxylem. The different anatomical features, as well as their evolution along the root type add significant variation to the kr estimation in between root type and along the root axe. Under the prism of root types, anatomy, and hydrophobic barriers, our results highlight the diversity of root radial and axial hydraulic conductivities, which may be veiled under low-resolution measurements of the root system hydraulic conductivity. While predictions of our root hydraulic maps match the range and trend of measurements reported in the literature, future studies could focus on the quantitative validation of hydraulic maps. From now on, a novel method, which turns root cross-section images into hydraulic maps will offer an inexpensive and easily applicable investigation tool for root hydraulics, in parallel to root pressure probing experiments. One-Sentence summaryThe use of cross-section images and modelling tools to generate a map the axial and radial hydraulic conductivity along different root types for the maize cultivar B73.
Why it matches plant phenotyping methods根の断面画像から解剖学的形質を抽出し、モデルで軸方向・半径方向の根 hydraulic conductivity を推定する手法が研究の中心であるため、植物表現型計測手法として収録する。
abstractWe used the Generator of Root Anatomy in R (GRANAR) model to generate root anatomical networks from anatomical features. Then we used the Model of Explicit Cross-section Hydraulic Anatomy (MECHA) to compute an estimation of the root axial and radial hydraulic conductivities (kx and kr, respectively)
Reproduction assets foundThe paper provides two public, paper-specific assets: the GRANAR-MECHA coupling workflow (Jupyter/R repository with Zenodo DOI) and the B73_HydraulicMap repository containing the Rmarkdown script used to compute the root hydraulic maps plus all input and output data of the study.Code · publicection can be visualized through different figures that show the
186 proportion of the water fluxes in each compartiment (apoplastic and symplastic fluxes).
The whole script that was used to compute the root hydraulic maps from the root anatomical
188 measurement is presented as a Rmarkdown script stored in a GitHub repository
(https://github.com/granar/B73_HydraulicMap doi: 10.5281/zenodo.4320861). In the same
190 repository are stored all input and output data of this study.
192
10 of 24
.
CC-BY 4.0 International license
perpetuity. It is made available under a
preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint Open asset ↗granar/B73_HydraulicMap · 10.5281/zenodo.4320861pdf-raw-page:10 lines:1-20Code / dataset availability confirmedEurope PMC · bioRxiv · checked 9 Sept 2026
Summary Soil is a heterogenous reservoir of essential elements needed for plant growth and development. Plants have evolved mechanisms to balance their nutritional needs based on availability of nutrients. This has led to genetically-based variation in the elemental composition ‘ionome’, of plants, both within and between species. We explore this natural variation using a panel of wild-collected, geographically widespread Arabidopsis thaliana accessions from the 1001 Genomes Project including over 1,135 accessions, and the 19 parental accessions of the Multi-parent Advanced Generation Inter-Cross (MAGIC) panel, all with full-genome sequences available. We present an experimental design pipeline for high-throughput ionomic screenings and analyses with improved normalisation procedures to account for errors and variability in conditions often encountered in large-scale, high-throughput data collection. We report quantification of the complete leaf and seed ionome of the entire collection using this pipeline and a digital tool-IonExplorer to interact with the dataset. We describe the pattern of natural ionomic variation across the A. thaliana species and identify several accessions with extreme ionomic profiles. It forms a valuable resource for exploratory QTL, GWA studies to identify genes underlying natural variation in leaf and seed ionome and genetic adaptation of plants to soil conditions.
Why it matches plant phenotyping methods大規模植物イオノーム取得のための高スループット実験・正規化パイプラインとデジタルツールを開発し、再利用可能なデータ資源として提示しているため、測定法が中心的です。
abstractWe present an experimental design pipeline for high-throughput ionomic screenings and analyses with improved normalisation procedures to account for errors and variability in conditions often encountered in large-scale, high-throughput data collection.
Reproduction assets foundThe paper's species-wide leaf and seed ionomic dataset for 1,135 A. thaliana accessions is made publicly accessible through the authors' interactive web tool Ion Explorer, which allows filtering, analysis, and download of the complete dataset as .csv files. This is a paper-specific, public, actionable asset. No author-Dataset · publicwe present an interactive web-based tool made available online: Ion Explorer
https://ffionexplorer.nottingham.ac.uk/ionmap/. Ion Explorer allows interactive visualisation,
analysis and comparison of the two large datasets.Open asset ↗Ion Explorerpdf-page:11 lines:1-44Code / dataset availability confirmedEurope PMC · checked 9 Sept 2026
Arbuscular mycorrhizal fungi function as conduits for underground nutrient transport. While the fungal partner is dependent on the plant host for its carbon (C) needs, the amount of nutrients that the fungus allocates to hosts can vary with context. Because fungal allocation patterns to hosts can change over time, they have historically been difficult to quantify accurately. We developed a technique to tag rock phosphorus (P) apatite with fluorescent quantum-dot (QD) nanoparticles of three different colors, allowing us to study nutrient transfer in an in vitro fungal network formed between two host roots of different ages and different P demands over a 3-week period. Using confocal microscopy and raster image correlation spectroscopy, we could distinguish between P transfer from the hyphae to the roots and P retention in the hyphae. By tracking QD-apatite from its point of origin, we found that the P demands of the younger root influenced both: (1) how the fungus distributed nutrients among different root hosts and (2) the storage patterns in the fungus itself. Our work highlights that fungal trade strategies are highly dynamic over time to local conditions, and stresses the need for precise measurements of symbiotic nutrient transfer across both space and time.
Why it matches plant phenotyping methods量子ドット標識と共焦点画像解析を開発し、植物根へのリン移行および菌根内保持を時空間的に定量する手法が研究の中心であるため、植物の栄養生理状態を測定するフェノタイピング手法として含める。
abstractWe developed a technique to tag rock phosphorus (P) apatite with fluorescent quantum-dot (QD) nanoparticles of three different colors
Reproduction assets foundThe paper's authors publicly deposited all data, scripts, and analysis for this study in a GitHub repository, explicitly stated in the Methods. This is a paper-specific, publicly actionable code/data asset reproducing the paper's QD-apatite phenotyping measurements and statistical analysis.Code · publicWe performed all statistical analysis in R version 3.6.1 [ 48 ]. All data, scripts, and analysis are available at: https://github.com/anoukvantpadje/Two_roots .Open asset ↗anoukvantpadje/Two_rootslines:57-192Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Plant leaf stomata are the gatekeepers of the atmosphere-plant interface and are essential building blocks of land surface models as they control transpiration and photosynthesis. Although more stomatal trait data are needed to significantly reduce the error in these model predictions, recording these traits is time-consuming, and no standardized protocol is currently available. Some attempts were made to automate stomatal detection from photomicrographs; however, these approaches have the disadvantage of using classic image processing or targeting a narrow taxonomic entity which makes these technologies less robust and generalizable to other plant species. We propose an easy-to-use and adaptable workflow from leaf to label. A methodology for automatic stomata detection was developed using deep neural networks according to the state of the art and its applicability demonstrated across the phylogeny of the angiosperms.We used a patch-based approach for training/tuning three different deep learning architectures. For training, we used 431 micrographs taken from leaf prints made according to the nail polish method from herbarium specimens of 19 species. The best-performing architecture was tested on 595 images of 16 additional species spread across the angiosperm phylogeny.The nail polish method was successfully applied in 78% of the species sampled here. The VGG19 architecture slightly outperformed the basic shallow and deep architectures, with a confidence threshold equal to 0.7 resulting in an optimal trade-off between precision and recall. Applying this threshold, the VGG19 architecture obtained an average F -score of 0.87, 0.89, and 0.67 on the training, validation, and unseen test set, respectively. The average accuracy was very high (94%) for computed stomatal counts on unseen images of species used for training.The leaf-to-label pipeline is an easy-to-use workflow for researchers of different areas of expertise interested in detecting stomata more efficiently. The described methodology was based on multiple species and well-established methods so that it can serve as a reference for future work.
Why it matches plant phenotyping methods葉の顕微画像から気孔を自動検出・計数する画像解析ワークフローを開発し、多様な植物種で性能検証しており、植物フェノタイピング手法が研究の中心です。
abstractA methodology for automatic stomata detection was developed using deep neural networks
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産2件を確認しました。Dataset · publicAll light microscope images used in this study are made freely accessible on Zenodo under the CC‐by license ( http://doi.org/10.5281/zenodo.3579227 ).Open asset ↗Zenodo · 10.5281/zenodo.3579227lines:186-229Dataset · publicThe example image set can also be downloaded here: http://doi.org/10.5281/zenodo.3902280 .Open asset ↗Zenodo · 10.5281/zenodo.3902280lines:186-229Code / dataset availability confirmedCrossref · checked 14 Sept 2026
Lignocellulosic biomass (LB) is recalcitrant to enzymatic hydrolysis due to its compact and complex cell wall structure. To identify the parameters behind LB recalcitrance, experimental data over hydrolysis time must be collected. Here, we describe a novel method to collect time-lapse images during cell wall deconstruction by enzymatic hydrolysis. The protocol includes instructions for sample preparation, layout of a custom designed incubation chamber and instructions for confocal time lapse acquisition. The protocol sets out a detailed plan where cross-sections of untreated and pretreated poplar samples are mounted in a sealed frame containing a buffer and an enzymatic cocktail. The sealed frame is then placed into an incubator to maintain the sample at a constant temperature of 50 °C, which is optimal for enzymatic reaction while avoiding enzymatic cocktail evaporation. Using lignin natural autofluorescence, confocal z-stacks of untreated and pretreated samples were acquired at regular time intervals during enzymatic hydrolysis for 24 h. Acquisition parameters were optimized to compromise between image resolution and reduced photo-bleaching. The acquired image might then be processed by further development of algorithms to extract precise quantitative information on cell wall deconstruction. This protocol is an important first step towards elucidating the underlying parameters of LB recalcitrance by allowing the acquisition of high-quality images of LB hydrolysis for extracting quantitative data on LB deconstruction.
Why it matches plant phenotyping methodsポプラ細胞壁の分解状態を時系列の共焦点3D画像で取得するプロトコル自体が中心であり、植物組織状態の定量的表現型抽出を可能にするため。
abstractHere, we describe a novel method to collect time-lapse images during cell wall deconstruction by enzymatic hydrolysis.
Reproduction assets foundThe paper's authors state that the scripts for computing photobleaching signal loss and image registration/analysis are publicly available in the FARE Laboratory GitLab repository, with an explicit URL matching an allowed URL.Code · publicels’ intensity
reduction in confocal image) between successive z-stacks. The signal loss was computed by subtracting
the voxels’ intensities between the registered floating image, It ◦ T It ←It+∆t , and the reference image It+∆t
and summing up the subtracted values (Scripts are available at the FARE Laboratory Gitlab Repository
https://gitlab.com/farelab/teamyr/publications/zoghlami_et_al_sus_chem_2020).
4. Results
Using the protocol, we acquired confocal images of pretreated poplar samples during hydrolysis
(Figure 7). We could visually observe that the cell walls gradually degraded over time. To illustrate
the advantages offered by using this protocol to achieve a quantitative characterizaOpen asset ↗gitlab.com/farelab/teamyr/publications/zoghlami_et_al_sus_chem_2020pdf-layout-page:8 lines:1-42Code / dataset availability confirmedEurope PMC · checked 9 Sept 2026
Laboratory / benchtopSeed / grainCountingGrowth / development / phenology
Background Plant parasitic weeds belonging to the genus Striga are a major threat for food production in Sub-Saharan Africa and Southeast Asia. The parasite's life cycle starts with the induction of seed germination by host plant-derived signals, followed by parasite attachment, infection, outgrowth, flowering, reproduction, seed set and dispersal. Given the small seed size of the parasite ( Striga seed germination. Results Here, we introduce DiSCount ( Di gital S triga Count er): a computer vision tool for automated quantification of total and germinated Striga seed numbers in standard glass fibre filter assays. We developed the software using a machine learning approach trained with a dataset of 98 manually annotated images. Then, we validated and tested the model against a total dataset of 188 manually counted images. The results showed that DiSCount has an average error of 3.38 percentage points per image compared to the manually counted dataset. Most importantly, DiSCount achieves a 100 to 3000-fold speed increase in image analysis when compared to manual analysis, with an inference time of approximately 3 s per image on a single CPU and 0.1 s on a GPU. Conclusions DiSCount is accurate and efficient in quantifying total and germinated Striga seeds in a standardized germination assay. This automated computer vision tool enables for high-throughput, large-scale screening of chemical compound libraries and biological control agents of this devastating parasitic weed. The complete software and manual are hosted at https://gitlab.com/lodewijk-track32/discount_paper and the archived version is available at Zenodo with the DOI 10.5281/zenodo.3627138. The dataset used for testing is available at Zenodo with the DOI 10.5281/zenodo.3403956.
Why it matches plant phenotyping methodsStriga種子の発芽状態を画像から自動定量するコンピュータビジョン手法の開発・検証が研究の中心であり、植物状態の表現型取得に該当する。
abstractwe introduce DiSCount ( Di gital S triga Count er): a computer vision tool for automated quantification of total and germinated Striga seed numbers
Reproduction assets foundThe paper's DiSCount software (code, manual, trained YOLOv3 model) is hosted on GitLab and archived on Zenodo; the manually counted test image dataset and the installation-test input dataset are also publicly available on Zenodo. The pytorch-yolo-v3 repository is a third-party code base, not a paper-specific asset.Code · publicThe complete software and manual are hosted at https://gitlab.com/lodewijk-track32/discount_paper and the archived version is available at Zenodo with the DOI https://doi.org/10.5281/zenodo.3627138 .Open asset ↗lodewijk-track32/discount_paperlines:1-79Code · publicThe DiSCount software is available at https://doi.org/10.5281/zenodo.3627138 along with detailed training settings and a complete installation and user manual.Open asset ↗10.5281/zenodo.3627138lines:84-90Dataset · publicThe dataset analysed to assess the performance of the software is publically available at https://doi.org/10.5281/zenodo.3403956 .Open asset ↗10.5281/zenodo.3403956lines:122-173Dataset · publicThe input dataset used to test the installation of the software is publically available at https://doi.org/10.5281/zenodo.3404131 .Open asset ↗10.5281/zenodo.3404131lines:122-173Code / dataset availability confirmedCrossref · checked 14 Sept 2026
CottonMaizeLaboratory / benchtopRootStem / branch2D/3D reconstructionRoot system architecture
Abstract Aims The flow of electric current in the root-soil system relates to the pathways of water and solutes, its characterization provides information on the root architecture and functioning. We developed a current source density approach with the goal of non-invasively image the current pathways in the root-soil system. Methods A current flow is applied from the plant stem to the soil, the proposed geoelectrical approach images the resulting distribution and intensity of the electric current in the root-soil system. The numerical inversion procedure underlying the approach was tested in numerical simulations and laboratory experiments with artificial metallic roots. We validated the method using rhizotron laboratory experiments on maize and cotton plants. Results Results from numerical and laboratory tests showed that our inversion approach was capable of imaging root-like distributions of the current source. In maize and cotton, roots acted as “leaky conductors”, resulting in successful imaging of the root crowns and negligible contribution of distal roots to the current flow. In contrast, the electrical insulating behavior of the cotton stems in dry soil supports the hypothesis that suberin layers can affect the mobility of ions and water. Conclusions The proposed approach with rhizotrons studies provides the first direct and concurrent characterization of the root-soil current pathways and their relationship with root functioning and architecture. This approach fills a major gap toward non-destructive imaging of roots in their natural soil environment.
Why it matches plant phenotyping methods根圏の電流経路を非侵襲的に画像化し、根の構造・機能を推定する新規手法を開発・検証しており、植物フェノタイピング手法が研究の中心である。
abstractWe developed a current source density approach with the goal of non-invasively image the current pathways in the root-soil system.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産2件を確認しました。Code · publicERT and iCSD codes, with data from this study, are maintained at https://github.com/Peruz/ERTpm and https://github.com/Peruz/icsd .Open asset ↗Peruz/ERTpmlines:342-431Code · publicERT and iCSD codes, with data from this study, are maintained at https://github.com/Peruz/ERTpm and https://github.com/Peruz/icsd .Open asset ↗Peruz/icsdlines:342-431Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Field / plotLaboratory / benchtopRootMorphology / geometry measurementRoot system architecture
Premise We developed a novel low-cost method to visually phenotype belowground structures in the plant rhizosphere. We devised the method introduced here to address the difficulties encountered growing plants in seed germination pouches for long-term experiments and the high cost of other mini-rhizotron alternatives. Methods and results The method described here took inspiration from homemade ant farms commonly used as an educational tool in elementary schools. Using compact disc (CD) cases, we developed mini-rhizotrons for use in the field and laboratory using the burclover Medicago lupulina . Conclusions Our method combines the benefits of pots and germination pouches. In CD mini-rhizotrons, plants grew significantly larger than in germination pouches, and unlike pots, it is possible to measure roots without destructive sampling. Our protocol is a cheaper, widely available alternative to more destructive methods, which could facilitate the study of belowground phenotypes and processes by scientists with fewer resources.
Why it matches plant phenotyping methods植物根系表現型を非破壊的に観察・測定する低コスト mini-rhizotron 法の開発が研究の中心であるため、収載対象。
abstractWe developed a novel low-cost method to visually phenotype belowground structures in the plant rhizosphere.
Reproduction assets foundThe paper's DATA AVAILABILITY statement deposits the root-phenotyping measurement data and the authors' R analysis scripts on Figshare. The analysis code DOI (10.6084/m9.figshare.12021084) matches an allowed URL; the data DOI (12021075) does not appear verbatim in the allowed URL list, so only the analysis asset is audCode · publics Davis, and Nick Mihailoff provided vital logistical
support at the Pymatuning Laboratory of Ecology; Laurie Follweiler
assisted with the growth chambers.
DATA AVAILABILITY
The data and associated R scripts are available through the open ac-
cess repository Figshare (data: https://doi.org/10.6084/m9.figsh
are.12021075;analysis:https://doi.org/10.6084/m9.figshare.12021084).LITERATURE CITED
Atamian, H. S., P. A. Roberts, and I. Kaloshian. 2012. High and low through-
put screens with root-knot nematodes Meloidogyne spp. JoVE (Journal ofOpen asset ↗Figshare · 10.6084/m9.figshare.12021084pdf-raw-page:5 lines:1-79Code / dataset availability confirmedOpenAlex · Europe PMC · Crossref · checked 9 Sept 2026
Hyperspectral imaging techniques have been expanding considerably in recent years. The cost of current solutions is decreasing, but these high-end technologies are not yet available for moderate to low-cost outdoor and indoor applications. We have used some of the latest compressive sensing methods with a single-pixel imaging setup. Projected patterns were generated on Fourier basis, which is well-known for its properties and reduction of acquisition and calculation times. A low-cost, moderate-flow prototype was developed and studied in the laboratory, which has made it possible to obtain metrologically validated reflectance measurements using a minimal computational workload. From these measurements, it was possible to discriminate plant species from the rest of a scene and to identify biologically contrasted areas within a leaf. This prototype gives access to easy-to-use phenotyping and teaching tools at very low-cost.
Why it matches plant phenotyping methods低コスト単一画素ハイパースペクトル撮像プロトタイプを開発し、反射率測定を計量学的に検証して植物フェノタイピングへの利用を示しており、測定手法が研究の中心である。
abstractA low-cost, moderate-flow prototype was developed and studied in the laboratory
Reproduction assets foundThe paper's supplementary materials publicly host the two hyperspectral hypercube datasets (leaf discrimination and leaf health-state experiments) directly used for the paper's phenotyping measurements, and the authors' acquisition/reconstruction MATLAB scripts are publicly available on a GitHub repository. Both are onDataset · publicThe following are available online at https://www.mdpi.com/1424-8220/20/4/1132/s1 , Data S1: “discrimination of a leaf within a scene” hypercube, Data S2: “different health states leaf” hypercube, Video S1: “discrimination of a leaf within a scene” hypercubeOpen asset ↗lines:64-76Code · publicAcquisition and reconstruction MATLAB ® scripts are available at https://github.com/mathieuribes/Hyperspectral-Single-Pixel-Imaging- .Open asset ↗github.com/mathieuribes/Hyperspectral-Single-Pixel-Imaging-lines:64-76Code / dataset availability confirmedEurope PMC · Crossref · OpenAlex · checked 15 Sept 2026
The rapid selection of salinity-tolerant crops to increase food production in salinized lands is important for sustainable agriculture. Recently, high-throughput plant phenotyping technologies have been adopted that use plant morphological and physiological measurements in a non-destructive manner to accelerate plant breeding processes. Here, a hyperspectral imaging (HSI) technique was implemented to monitor the plant phenotypes of 13 okra (Abelmoschus esculentus L.) genotypes after 2 and 7 days of salt treatment. Physiological and biochemical traits, such as fresh weight, SPAD, elemental contents and photosynthesis-related parameters, which require laborious, time-consuming measurements, were also investigated. Traditional laboratory-based methods indicated the diverse performance levels of different okra genotypes in response to salinity stress. We introduced improved plant and leaf segmentation approaches to RGB images extracted from HSI imaging based on deep learning. The state-of-the-art performance of the deep-learning approach for segmentation resulted in an intersection over union score of 0.94 for plant segmentation and a symmetric best dice score of 85.4 for leaf segmentation. Moreover, deleterious effects of salinity affected the physiological and biochemical processes of okra, which resulted in substantial changes in the spectral information. Four sample predictions were constructed based on the spectral data, with correlation coefficients of 0.835, 0.704, 0.609 and 0.588 for SPAD, sodium concentration, photosynthetic rate and transpiration rate, respectively. The results confirmed the usefulness of high-throughput phenotyping for studying plant salinity stress using a combination of HSI and deep-learning approaches.
Why it matches plant phenotyping methodsHSIと深層学習による植物・葉のセグメンテーションおよび生理形質推定が研究の中心であり、高スループット表現型取得手法を実装・評価している。
titleHyperspectral imaging combined with machine learning as a tool to obtain high‐throughput plant salt‐stress phenotyping
Reproduction assets foundThe authors publicly deposited the plant/leaf segmentation models in CodeOcean and the MMD clustering source code on GitHub, both directly supporting this paper's phenotyping analysis. The CVPPP 2015 dataset and Hitachi annotation tool are third-party/generic resources, not paper-specific assets.Code · publicels were constructed using Python3.6 (Guido van Ros-
sum, Python Dev Team).
DATA AVAILABILITY STATEMENT
Data further supporting this work, such as details of plant
and leaf segmentation models used in this study, are open
and available in codeocean (https://doi.org/10.24433/CO.3430273.v1). The source code of MMD is available on
https://github.com/jinnuozhang/Coderoom/blob/master/CLUS
TER.ipynb.
ACKNOWLEDGEMENT
The authors would like to thank Hui Fang for helping in illustrat-
ing.
CONFLICT OF INTEREST
The authors declare no conflicts of interest.
AUTHOR CONTRIBUTIONS
XF designed the research. YH and DJ supervised the pro-
ject. XF, YZ, XY, CY, HW and ZT performed the experi-
ments. QW analyzOpen asset ↗github.com/jinnuozhang/Coderoompdf-raw-page:13 lines:1-89Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Conventional methods for screening for stress-tolerant cereal varieties rely on expensive, labour-intensive field testing and molecular biology techniques. Here, we use the root hair assay (RHA) as a rapid screening tool to identify stress-tolerant varieties at the early seedling stage. Wheat and barley seedlings had stress applied, and the response quantified in terms of programmed cell death (PCD), viability and necrosis. Heat shock experiments of seven barley varieties showed that winter and spring barley varieties could be partitioned into their two distinct seasonal groups based on their PCD susceptibility, allowing quick data-driven evaluation of their thermotolerance at an early seedling stage. In addition, evaluating the response of eight wheat varieties to heat and salt stress allowed identification of their PCD inflection points (35°C and 150 mM NaCl), where the largest differences in PCD levels arise. Using the PCD inflection points as a reference, we compared different stress effects and found that heat-susceptible wheat varieties displayed similar vulnerabilities to salt stress. Stress-induced PCD levels also facilitated the assessment of the basal, induced and cross-stress tolerance of wheat varieties using single, combined and multiple individual stress exposures by applying concurrent heat and salt stress in a time-course experiment. Two stress-susceptible varieties were found to have low constitutive resistance as illustrated by their high PCD levels in response to single and combined stress exposure. However, both varieties had a fast, adaptive response as PCD levels declined at the other time-points, showing that even with low constitutive resistance, the initial stress cue primes cross-stress tolerance adaptations for enhanced resistance even to a second, different stress type. Here, we demonstrate the RHA's suitability for high-throughput analysis (∼4 days from germination to data collection) of multiple cereal varieties and stress treatments. We also showed the versatility of using stress-induced PCD levels to investigate the role of constitutive and adaptive resistance by exploring the temporal progression of cross-stress tolerance. Our results show that by identifying suboptimal PCD levels in vivo in a laboratory setting, we can preliminarily identify stress-susceptible cereal varieties and this information can guide further, more efficiently targeted, field-scale experimental testing.
Why it matches plant phenotyping methods根毛アッセイ（RHA）を用いてストレス誘導性PCD・生存性・壊死を定量し、作物品種の耐性を迅速かつハイスループットにスクリーニングする手法を実証しており、表現型取得法が研究の中心である。
abstractHere, we use the root hair assay (RHA) as a rapid screening tool to identify stress-tolerant varieties at the early seedling stage.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Supplement · publicAll datasets generated for this study are included in the article/ Supplementary Material .Open asset ↗lines:703-766Code / dataset availability confirmedEurope PMC · checked 9 Sept 2026
Background As yields of major crops such as wheat ( T. aestivum ) have begun to plateau in recent years, there is growing pressure to efficiently phenotype large populations for traits associated with genetic advancement in yield. Photosynthesis encompasses a range of steady state and dynamic traits that are key targets for raising Radiation Use Efficiency (RUE), biomass production and grain yield in crops. Traditional methodologies to assess the full range of responses of photosynthesis, such a leaf gas exchange, are slow and limited to one leaf (or part of a leaf) per instrument. Due to constraints imposed by time, equipment and plant size, photosynthetic data is often collected at one or two phenological stages and in response to limited environmental conditions. Results Here we describe a high throughput procedure utilising chlorophyll fluorescence imaging to phenotype dynamic photosynthesis and photoprotection in excised leaves under controlled gaseous conditions. When measured throughout the day, no significant differences ( P > 0.081) were observed between the responses of excised and intact leaves. Using excised leaves, the response of three cultivars of T. aestivum to a user-defined dynamic lighting regime was examined. Cultivar specific differences were observed for maximum PSII efficiency ( F v '/ F m '- P F q '/ F m '- P = 0.04) under both low and high light. In addition, the rate of induction and relaxation of non-photochemical quenching (NPQ) was also cultivar specific. A specialised imaging chamber was designed and built in-house to maintain gaseous conditions around excised leaf sections. The purpose of this is to manipulate electron sinks such as photorespiration. The stability of carbon dioxide (CO 2 ) and oxygen (O 2 ) was monitored inside the chambers and found to be within ± 4.5% and ± 1% of the mean respectively. To test the chamber, T. aestivum 'Pavon76' leaf sections were measured under at 20 and 200 mmol mol -1 O 2 and ambient [CO 2 ] during a light response curve. The F v '/ F m 'was significantly higher ( P 2 ] for the majority of light intensities while values of NPQ and the proportion of open PSII reaction centers (qP) were significantly lower under > 130 μmol m -2 s -1 photosynthetic photon flux density (PPFD). Conclusions Here we demonstrate the development of a high-throughput (> 500 samples day -1 ) method for phenotyping photosynthetic and photo-protective parameters in a dynamic light environment. The technique exploits chlorophyll fluorescence imaging in a specifically designed chamber, enabling controlled gaseous environment around leaf sections. In addition, we have demonstrated that leaf sections do not different from intact plant material even > 3 h after sampling, thus enabling transportation of material of interest from the field to this laboratory based platform. The methodologies described here allow rapid, custom screening of field material for variation in photosynthetic processes.
Why it matches plant phenotyping methods葉緑素蛍光イメージングと専用チャンバーを用いた高スループットな光合成・光防御形質の取得法を開発し、葉およびチャンバー条件を検証しているため、植物フェノタイピング手法が中心である。
abstractHere we describe a high throughput procedure utilising chlorophyll fluorescence imaging to phenotype dynamic photosynthesis and photoprotection in excised leaves under controlled gaseous conditions.
Reproduction assets foundThe paper's phenotyping pipeline (chlorophyll fluorescence imaging of excised wheat leaves in custom gas-controlled chambers) is supported by a paper-specific public asset: Additional file 2, a ZIP supplement containing the CAD files, printer settings, and construction notes for the custom imaging chambers, explicitly'Supplement · publicThe CAD files for the final chamber design are fully available with this manuscript (Additional file 2 ) including printer settings and additional notes, so that users can either print their own, outsource the printing or modify the designs.Open asset ↗lines:94-102Code / dataset availability confirmedEurope PMC · OpenAlex · Crossref · checked 14 Sept 2026
Powdery mildews present specific challenges to phenotyping systems that are based on imaging. Having previously developed low-throughput, quantitative microscopy approaches for phenotyping resistance to Erysiphe necator on thousands of grape leaf disk samples for genetic analysis, here we developed automated imaging and analysis methods for E. necator severity on leaf disks. By pairing a 46-megapixel CMOS sensor camera, a long-working distance lens providing 3.5× magnification, X-Y sample positioning, and Z-axis focusing movement, the system captured 78% of the area of a 1-cm diameter leaf disk in 3 to 10 focus-stacked images within 13.5 to 26 seconds. Each image pixel represented 1.44 μ m 2 of the leaf disk. A convolutional neural network (CNN) based on GoogLeNet determined the presence or absence of E. necator hyphae in approximately 800 subimages per leaf disk as an assessment of severity, with a training validation accuracy of 94.3%. For an independent image set the CNN was in agreement with human experts for 89.3% to 91.7% of subimages. This live-imaging approach was nondestructive, and a repeated measures time course of infection showed differentiation among susceptible, moderate, and resistant samples. Processing over one thousand samples per day with good accuracy, the system can assess host resistance, chemical or biological efficacy, or other phenotypic responses of grapevine to E. necator . In addition, new CNNs could be readily developed for phenotyping within diverse pathosystems or for diverse traits amenable to leaf disk assays.
Why it matches plant phenotyping methodsブドウ葉ディスク上のうどんこ病重症度を画像とCNNで定量する高スループット表現型解析システムを開発・検証しており、植物表現型取得法が研究の中心である。
abstracthere we developed automated imaging and analysis methods for E. necator severity on leaf disks
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicThe imaging control software is available at https://github.com/LightingResearchCenter/Plant-Imaging- Platform .Open asset ↗LightingResearchCenter/Plant-Imaging- · Plant-Imaging-lines:359-372Code / dataset availability confirmedEurope PMC · OpenAlex · bioRxiv · checked 9 Sept 2026
Hypocotyl length determination is a widely used method to phenotype young seedlings. The measurement itself has been developed from using rulers and millimeter papers to the assessment of digitized images, yet it remained a labour-intensive, monotonous and time consuming procedure. To make high-throughput plant phenotyping possible, we developed a deep learning-based approach to simplify and accelerate this method. Our pipeline does not require a specialized imaging system but works well with low quality images, produced with a simple flatbed scanner or a smartphone camera. Moreover, it is easily adaptable for a diverse range of datasets, not restricted to Arabidopsis thaliana . Furthermore, we show that the accuracy of the method reaches human performance. We not only provide the full code at https://github.com/biomag-lab/hypocotyl-UNet , but also give detailed instructions on how the algorithm can be trained with custom data, tailoring it for the requirements and imaging setup of the user. One-sentence summary A deep learning-based algorithm, providing an adaptable tool for determining hypocotyl or coleoptile length of different plant species.
Why it matches plant phenotyping methods幼植物の表現型である胚軸・子葉鞘長を画像から高スループットに推定する深層学習手法を開発しており、表現型取得・抽出法が研究の中心である。
abstractTo make high-throughput plant phenotyping possible, we developed a deep learning-based approach to simplify and accelerate this method.
Reproduction assets foundThe paper explicitly states that the full open-source analysis code (U-Net-based hypocotyl segmentation/measurement pipeline) is available on GitHub and that the training images (annotated Arabidopsis, Sinapis, Brachypodium seedling images) are publicly available on Kaggle. Both are paper-specific, public, and directlyCode · publicThe code is fully open source and available at GitHub
(https://github.com/biomag-lab/hypocotyl-UNet).Open asset ↗biomag-lab/hypocotyl-UNetpdf-page:9 lines:1-56Dataset · publicImages used for training are also available
at https://www.kaggle.com/tivadardanka/plant-segmentation.Open asset ↗pdf-page:9 lines:1-56Code / dataset availability confirmedarXiv · OpenAlex · checked 14 Sept 2026
Images are used frequently in plant phenotyping to capture measurements. This chapter offers a repeatable method for capturing two-dimensional measurements of plant parts in field or laboratory settings using a variety of camera styles (cellular phone, DSLR), with the addition of a printed calibration pattern. The method is based on calibrating the camera using information available from the EXIF tags from the image, as well as visual information from the pattern. Code is provided to implement the method, as well as a dataset for testing. We include steps to verify protocol correctness by imaging an artifact. The use of this protocol for two-dimensional plant phenotyping will allow data capture from different cameras and environments, with comparison on the same physical scale. We abbreviate this method as CASS, for CAmera aS Scanner. Code and data is available at http://doi.org/10.5281/zenodo.3677473.
Why it matches plant phenotyping methods植物部位の2次元形質をカメラで測定する手法を開発し、校正・検証手順、コード、テストデータを提供しており、植物フェノタイピング手法が中心である。
abstractThis chapter offers a repeatable method for capturing two-dimensional measurements of plant parts in field or laboratory settings using a variety of camera styles (cellular phone, DSLR), with the addition of a printed calibration pattern.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Dataset · publicThe code and test datasets are provided in [ 16 ] . Within [ 16 ] , are some example data and two programs:
aruco-pattern-write and camera-as-scanner . To prepare for the experiments, download the example data and install the code (C++ code as well as a Docker image are provided).Open asset ↗lines:54-78Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
ArabidopsisLaboratory / benchtopRootMorphology / geometry measurementRoot system architecture
Root analysis is essential for both academic and agricultural research. Despite the great advances in root phenotyping and imaging, calculating root length is still performed manually and involves considerable amounts of labor and time. To overcome these limitations, we developed MyROOT, a software for the semiautomatic quantification of root growth of seedlings growing directly on agar plates. Our method automatically determines the scale from the image of the plate, and subsequently measures the root length of the individual plants. To this aim, MyROOT combines a bottom-up root tracking approach with a hypocotyl detection algorithm. At the same time as providing accurate root measurements, MyROOT also significantly minimizes the user intervention required during the process. Using Arabidopsis, we tested MyROOT with seedlings from different growth stages and experimental conditions. When comparing the data obtained from this software with that of manual root measurements, we found a high correlation between both methods (R 2 = 0.997). When compared with previous developed software with similar features (BRAT and EZ-Rhizo), MyROOT offered an improved accuracy for root length measurements. Therefore, MyROOT will be of great use to the plant science community by permitting high-throughput root length measurements while saving both labor and time.
Why it matches plant phenotyping methods根長を画像から半自動抽出するソフトウェアを開発し、手動測定および既存ソフトウェアと比較検証しており、植物フェノタイピング手法が研究の中心である。
abstractwe developed MyROOT, a software for the semiautomatic quantification of root growth of seedlings growing directly on agar plates.
Reproduction assets foundThe authors deposited the MyROOT standalone executable application together with the root-length datasets generated in the study (Figures 3, 5 and S4) in a Zenodo repository with an explicit public DOI, making it a paper-specific, publicly actionable asset.Dataset · publiclable to the plant sciences community through the Plant Image Analysis website (plant‐image‐analysis.org; Lobet et al ., 2013 ) as a standalone executable application. The executable application together with the datasets generated during the current study (from Figures 3 , 5 and S4 ) are available in the [Zenodo] repository, [ https://doi.org/10.5281/zenodo.2552250 ].
Conflict of Interest
The authors declare no conflicts of interest.
Author Contributions
AIC‐D conceived the idea. AG and XS developed the algorithms for the method. AG, XS, IB‐P and DB‐E performed the validation experiments. IB‐P and DB‐E acquired the dataset. XS and AIC‐D designed and supervised the study. IB‐P, AG, XS andOpen asset ↗Zenodo · 10.5281/zenodo.2552250lines:139-168Code / dataset availability confirmedEurope PMC · checked 10 Sept 2026
The endoplasmic reticulum (ER) is a highly dynamic polygonal membrane network composed of interconnected tubules and sheets (cisternae) that forms the first compartment in the secretory pathway involved in protein translocation, folding, glycosylation, quality control, lipid synthesis, calcium signalling, and metabolon formation. Despite its central role in this plethora of biosynthetic, metabolic and physiological processes, there is little quantitative information on ER structure, morphology or dynamics. Here we describe a software package (AnalyzER) to automatically extract ER tubules and cisternae from multi-dimensional fluorescence images of plant ER. The structure, topology, protein-localisation patterns, and dynamics are automatically quantified using spatial, intensity and graph-theoretic metrics. We validate the method against manually-traced ground-truth networks, and calibrate the sub-resolution width estimates against ER profiles identified in serial block-face SEM images. We apply the approach to quantify the effects on ER morphology of drug treatments, abiotic stress and over-expression of ER tubule-shaping and cisternal-modifying proteins.
Why it matches plant phenotyping methods植物ERの蛍光画像から構造・形態・動態を自動抽出・定量するソフトウェアを開発し、手動トレースおよびSEM画像で検証・較正しているため、植物表現型計測手法が中心である。
abstractHere we describe a software package (AnalyzER) to automatically extract ER tubules and cisternae from multi-dimensional fluorescence images of plant ER.
Reproduction assets foundThe authors deposited the AnalyzER MATLAB software (with manual, tutorial, and test data) plus all images, parameter files, and analysis results in the Oxford Research Archive at a public URL, directly reproducing this paper's plant ER phenotyping analysis.Dataset · publicAll images, parameter files used in the software to analyse them, and the results are available from the Oxford Research Archive (ORA) ( https://ora.ox.ac.uk/objects/uuid:cb0e2845-2a9c-495a-84f0-4dd2c5164463 ).Open asset ↗Oxford Research Archive (ORA) · uuid:cb0e2845-2a9c-495a-84f0-4dd2c5164463lines:161-264Code / dataset availability confirmedbioRxiv · Crossref · checked 15 Sept 2026
BackgroundOne of the main features of plant cells is their strong plasticity, and their propensity to regenerate an organism from a single cell. Plant protoplasts are basic plant cells units in which the pecto-cellulosic cell wall has been removed, but the plasma membrane is intact. One of the main features of plant cells is their strong plasticity, which in some species, can be very close from what is defined as cell totipotency. Methods and differentiation protocols used in plant physiology and plant biology usually involve macroscopic vessels and containers that make difficult, for example, to follow the fate of the same protoplast all along its full development cycle, but also to perform continuous studies of the influence of various gradients in this context. These limits have hampered the precise study of regeneration processes. ResultsHerein, we present the design of a comprehensive, physiologically relevant, easy-to-use and low-cost microfluidic and microscopic setup for the monitoring of Physcomitrella patens (P. patens) growth and development on a long-term basis. The experimental solution we developed is made of two parts (i) a microfluidic chip composed of a single layer of about a hundred flow-through microfluidic traps for the immobilization of protoplasts, and (ii) a low-cost, light-controlled, custom-made microscope allowing the continuous recording of the moss development in physiological conditions. We validated the experimental setup with three proofs of concepts: (i) the kinetic monitoring of first division steps and cell wall regeneration, (ii) the influence of the photoperiod on growth of the protonemata, and (iii) finally the induction of leafy buds using a phytohormone, cytokinin. ConclusionsWe developed the design of a comprehensive, physiologically relevant, easy-to-use and low-cost experimental setup for the study of P. patens development in a microfluidic environment. This setup allows imaging of P. patens development at high resolution and over long time periods.
Why it matches plant phenotyping methods植物の発生・成長を長期間画像モニタリングするマイクロ流体チップとカスタム顕微鏡を開発しており、表現型取得系が研究の中心である。
abstractwe present the design of a comprehensive, physiologically relevant, easy-to-use and low-cost microfluidic and microscopic setup for the monitoring of Physcomitrella patens (P. patens) growth and development on a long-term basis.
Reproduction assets foundThe paper's availability statement points to a public GitHub repository (FattaccioliLab/PlantsOnChip) containing the authors' microfluidic chip design files, microscope control Matlab scripts, Micromanager configuration, Arduino connection map, and bill of materials used for the plant protoplast phenotyping/imaging. NoCode · publicfile of the 35 mm Petri dish adapter to the SM1 threading of the xy manual stage
• Matlab programming script of the microscope and Micromanager configuration file
• Connection map of the Arduino Due board
• Bill of materials of the custom-made microscope (references, manufacturers, suppliers, prices)
Documents are available on https://github.com/FattaccioliLab/PlantsOnChip
Supplementary movies.
• Division of a protoplast and cell wall regeneration kinetics
• Chloronemata growth under continuous illumination
Competing interests. No financial competing interests are to be declared.
Funding. This work has received support of “Institut Pierre-Gilles de Gennes” (Laboratoire
d’excellence : ANR-10-Open asset ↗FattaccioliLab/PlantsOnChippdf-raw-page:11 lines:1-29Code / dataset availability confirmedEurope PMC · checked 10 Sept 2026
Background Remote monitoring of plants using hyperspectral imaging has become an important tool for the study of plant growth, development, and physiology. Many applications are oriented towards use in field environments to enable non-destructive analysis of crop responses due to factors such as drought, nutrient deficiency, and disease, e.g., using tram, drone, or airplane mounted instruments. The field setting introduces a wide range of uncontrolled environmental variables that make validation and interpretation of spectral responses challenging, and as such lab- and greenhouse-deployed systems for plant studies and phenotyping are of increasing interest. In this study, we have designed and developed an open-source, hyperspectral reflectance-based imaging system for lab-based plant experiments: the HyperScanner. The reliability and accuracy of HyperScanner were validated using drought and salt stress experiments with Arabidopsis thaliana . Results A robust, scalable, and reliable system was created. The system was built using open-sourced parts, and all custom parts, operational methods, and data have been made publicly available in order to maintain the open-source aim of HyperScanner. The gathered reflectance images showed changes in narrowband red and infrared reflectance spectra for each of the stress tests that was evident prior to other visual physiological responses and exhibited congruence with measurements using full-range contact spectrometers. Conclusions HyperScanner offers the potential for reliable and inexpensive laboratory hyperspectral imaging systems. HyperScanner was able to quickly collect accurate reflectance curves on a variety of plant stress experiments. The resulting images showed spectral differences in plants shortly after application of a treatment but before visual manifestation. HyperScanner increases the capacity for spectroscopic and imaging-based analytical tools by providing more access to hyperspectral analyses in the laboratory setting.
Why it matches plant phenotyping methods植物の表現型取得を目的とする低コスト・オープンソースのハイパースペクトル画像システムを開発し、植物ストレス実験で信頼性と精度を検証しており、手法が研究の中心である。
abstractwe have designed and developed an open-source, hyperspectral reflectance-based imaging system for lab-based plant experiments: the HyperScanner.
Reproduction assets foundThe paper's supporting datasets (growth-environment and hyperspectral reflectance data from the Arabidopsis drought/salt stress experiments) are publicly available in the authors' Cyverse repository; the authors' Ardupy control/analysis software is public on GitHub and archived on Zenodo; and the 3D model files are on Dataset · publicThe datasets supporting the conclusions of this article are available in the Cyverse repository ( https://de.cyverse.org/de/?type=data&folder=/iplant/home/elytas/experiment_repository ).Open asset ↗Cyverselines:379-449Code · publicThese tools, named Ardupy, have been made publicly available on the University of Wisconsin EnSpec organization’s Github page ( https://github.com/EnSpec/Plant_CNC_Controller ) as well as on Zenodo ( https://doi.org/10.5281/zenodo.1406721 )Open asset ↗GitHub · EnSpec/Plant_CNC_Controllerlines:138-145Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
Background The development of leaf area is one of the fundamental variables to quantify plant growth and physiological function and is therefore widely used to characterize genotypes and their interaction with the environment. To date, analysis of leaf area often requires elaborate and destructive measurements or imaging-based methods accompanied by automation that may result in costly solutions. Consequently in recent years there is an increasing trend towards simple and affordable sensor solutions and methodologies. A major focus is currently on harnessing the potential of applications developed for smartphones that provide access to analysis tools to a wide user basis. However, most existing applications entail significant manual effort during data acquisition and analysis. Results With the development of Plant Screen Mobile we provide a suitable smartphone solution for estimating digital proxies of leaf area and biomass in various imaging scenarios in the lab, greenhouse and in the field. To distinguish between plant tissue and background the core of the application comprises different classification approaches that can be parametrized by users delivering results on-the-fly. We demonstrate the practical applications of computing projected leaf area based on two case studies with Eragrostis and Musa plants. These studies showed highly significant correlations with destructive measurements of leaf area and biomass from both ground truth measurements and estimations from well-established screening systems. Conclusions We show that a smartphone together with our analysis tool Plant Screen Mobile is a suitable platform for rapid quantification of leaf and shoot development of various plant architectures. Beyond the estimation of projected leaf area the app can also be used to quantify color and shape parameters of other plant material including seeds and flowers.
Why it matches plant phenotyping methodsスマートフォン画像と分類アルゴリズムによる葉面積・バイオマス推定アプリを開発し、破壊測定および既存システムと検証しており、植物表現型取得が中心である。
abstractWith the development of Plant Screen Mobile we provide a suitable smartphone solution for estimating digital proxies of leaf area and biomass in various imaging scenarios in the lab, greenhouse and in the field.
Reproduction assets foundThe authors deposited the plant image data and corresponding ground truth measurements from the banana and Eragrostis case studies in the e!DAL research data publication system (DOI 10.25622/FZJ/2018/1), a paper-specific public asset. The project homepage (fz-juelich.de/ibg/ibg-2/psm) hosts the app and manual but is a Dataset · publichave no competing interests.
Availability of data and materials
The app is accompanied by a detailed manual and checkerboard images for calibration, which can also be downloaded from the project homepage. The datasets generated and/or analyzed during the current study are available in the e!DAL research data publication system, http://dx.doi.org/10.25622/FZJ/2018/1 [ 30 ].
Availability and requirements
Project name: Plant Screen Mobile. Project home page: https://fz-juelich.de/ibg/ibg-2/psm . Operating system(s): Android OS 4.0 (Ice Cream Sandwich) or higher. Programming language: Java. Other requirements: OpenCV manager (will be installed during Plant Screen Mobile setup). License: GNU GOpen asset ↗e!DAL research data publication system · 10.25622/FZJ/2018/1lines:127-198Code / dataset availability confirmedOpenAlex · Europe PMC · checked 10 Sept 2026
The mucilage is a model to study the polysaccharide biosynthesis since it is produced in large amounts and composed of complex polymers. In addition, it is of great economic interest for its technical and nutritional value. A fast method for phenotyping the released mucilage and the seed morphometric parameters will be useful for fundamental, food, pharmaceutical and breeding researches. Current strategies to phenotype soluble mucilage are restricted to visual evaluations or are highly time-consuming. Here, we developed a high-throughput phenotyping method for the simultaneous measurement of the soluble mucilage content released on a gel and the seed morphometric parameters. Within this context, we combined a biochemical assay and an open-source computer-aided image analysis tool, MuSeeQ. The biochemical assay consists in sowing seeds on an agarose medium containing the dye toluidine blue O, which specifically stains the mucilage once it is released on the gel. The second part of MuSeeQ is a macro developed in ImageJ allowing to quickly extract and analyse 11 morphometric data of seeds and their respective released mucilages. As an example, MuSeeQ was applied on a flax recombinant inbred lines population (previously screened for fatty acids content.) and revealed significant correlations between the soluble mucilage shape and the concentration of some fatty acids, e.g. C16:0 and C18:2. Other fatty acids were also found to correlate with the seed shape parameters, e.g. C18:0 and C18:2. MuSeeQ was then showed to be used for the analysis of other myxospermous species, including Arabidopsis thaliana and Camelina sativa. MuSeeQ is a low-cost and user-friendly method which may be used by breeders and researchers for phenotyping simultaneously seeds of specific cultivars, natural variants or mutants and their respective soluble mucilage area released on a gel. The script of MuSeeQ and video tutorials are freely available at http://MuSeeQ.free.fr .
Why it matches plant phenotyping methods種子形態と放出粘液を画像から同時測定する高スループット手法およびImageJツールを開発・適用しており、植物表現型取得が研究の中心である。
abstractHere, we developed a high-throughput phenotyping method for the simultaneous measurement of the soluble mucilage content released on a gel and the seed morphometric parameters.
Reproduction assets foundThe paper's MuSeeQ ImageJ macro (the authors' phenotyping analysis code) is explicitly stated to be freely available, with video tutorials, at the authors' dedicated public website http://MuSeeQ.free.fr, which appears in the allowed URLs.Code · publicThe script of MuSeeQ and video tutorials are freely available at http://MuSeeQ.free.fr .Open asset ↗MuSeeQ.free.frlines:1-73Code / dataset availability confirmedCrossref · checked 10 Sept 2026
Background and aims Non- or minimally invasive methods are urgently needed to characterize and monitor crop root systems to foster progress in phenotyping and general system understanding. Electrical methods have come into focus due to their unique sensitivity to various structural and functional root characteristics. The aim of this study is to highlight imaging capabilities of these methods with regard to crop root systems and to investigate changes in electrical signals caused by physiological reactions. Methods Spectral electrical impedance tomography (sEIT) and electrical impedance spectroscopy (EIS) were used in three laboratory experiments to characterize oilseed root systems embedded in nutrient solution. Two experiments imaged the root extension with sEIT, including one experiment monitoring a nutrient stress situation. In the third experiment electrical signatures were observed over the diurnal cycle using EIS. Results Root system extension was imaged using sEIT under static conditions. During continuous nutrient deprivation, electrical polarization signals decreased steadily. Systematic changes were observed over the diurnal cycle, indicating further sensitivity to associated physiological processes. Spectral parameters suggest polarization processes at the μm scale. Conclusions Electrical imaging methods are able to non-invasively characterize crop root systems in controlled laboratory conditions, thereby offering links to root structure and function. The methods have the potential to be upscaled to the field scale.
Why it matches plant phenotyping methods電気インピーダンス画像化・分光法を用いて作物根系の構造と生理状態を非侵襲的に測定する方法が研究の中心であり、根系伸長や栄養ストレス・日周生理変化の表現型取得を実証している。
abstractNon- or minimally invasive methods are urgently needed to characterize and monitor crop root systems to foster progress in phenotyping and general system understanding.
Reproduction assets foundThe paper's Data Availability statement explicitly deposits the sEIT/EIS measurement data and analysis scripts in a public Zenodo repository, which directly reproduces this paper's root-phenotyping measurements and computational analysis.Dataset · publicData Availability
Measurement data and analysis scripts are available under the https://doi.org/10.5281/zenodo.1320755Open asset ↗zenodo · 10.5281/zenodo.1320755lines:233-271Code / dataset availability confirmedOpenAlex · Europe PMC · checked 10 Sept 2026
The model species Arabidopsis thaliana has extensive resources to investigate intraspecific trait variability and the genetic bases of ecologically relevant traits. However, the cost of equipment and software required for high-throughput phenotyping is often a bottleneck for large-scale studies, such as mutant screening or quantitative genetics analyses. Simple tools are needed for the measurement of fitness-related traits, like relative growth rate and fruit production, without investment in expensive infrastructures. Here, we describe methods that enable the estimation of biomass accumulation and fruit number from the analysis of rosette and inflorescence images taken with a regular camera. We developed two models to predict plant dry mass and fruit number from the parameters extracted with the analysis of rosette and inflorescence images. Predictive models were trained by sacrificing growing individuals for dry mass estimation, and manually measuring a fraction of individuals for fruit number at maturity. Using a cross-validation approach, we showed that quantitative parameters extracted from image analysis predicts more 90% of both plant dry mass and fruit number. When used on 451 natural accessions, the method allowed modeling growth dynamics, including relative growth rate, throughout the life cycle of various ecotypes. Estimated growth-related traits had high heritability (0.65 < H 2 < 0.93), as well as estimated fruit number ( H 2 = 0.68). In addition, we validated the method for estimating fruit number with rev5 , a mutant with increased flower abortion. The method we propose here is an application of automated computerization of plant images with ImageJ, and subsequent statistical modeling in R. It allows plant biologists to measure growth dynamics and fruit number in hundreds of individuals with simple computing steps that can be repeated and adjusted to a wide range of laboratory conditions. It is thus a flexible toolkit for the measurement of fitness-related traits in large populations of a model species.
Why it matches plant phenotyping methods画像から植物乾物重・果実数・成長動態を推定する手法を開発し、交差検証と変異体で検証しており、表現型取得・推定法が研究の中心である。
abstractHere, we describe methods that enable the estimation of biomass accumulation and fruit number from the analysis of rosette and inflorescence images taken with a regular camera.
Reproduction assets foundThe paper's availability statement explicitly links authors' code on GitHub and the phenotypic dataset on Dryad; supplementary files also contain the ImageJ macros and R code used for the phenotyping analysis.Code · publicCodes are available on Github ( https://github.com/fvasseur ), and phenotypic data are available on the Dryad repository ( https://doi.org/10.5061/dryad.343bd84 ) [ 43 ].Open asset ↗github.com/fvasseurlines:312-394Dataset · publicphenotypic data are available on the Dryad repository ( https://doi.org/10.5061/dryad.343bd84 ) [ 43 ].Open asset ↗Dryad · 10.5061/dryad.343bd84lines:312-394Code / dataset availability confirmedbioRxiv · Europe PMC · Crossref · checked 14 Sept 2026
ArabidopsisLaboratory / benchtopRootMorphology / geometry measurementObject detectionTrackingRoot system architecture
Root analysis is essential for both academic and agricultural research. Despite the great advances in root phenotyping and imaging however, calculating root length is still performed manually and involves considerable amounts of labor and time. To overcome these limitations, we have developed MyROOT, a novel software for the semi-automatic quantification of root growth of seedlings growing directly in agar plates. Our method automatically determines the scale from the image of the plate, and subsequently measures the root length of the individual plants. To this aim, MyROOT combines a bottom-up root tracking approach with a hypocotyl detection algorithm. At the same time as providing accurate root measurements, MyROOT also significantly minimizes the user intervention required during the process. Using Arabidopsis, we tested MyROOT with seedlings from different growth stages. Upon comparing the data obtained using this software with that of manual root measurements, we found that there are no significant differences (t-test, p-value < 0.05). Thus, MyROOT will be of great aid to the plant science community by permitting high-throughput root length measurements while saving on both labor and time.
Why it matches plant phenotyping methods根長という植物形質の半自動画像計測ソフトウェアを開発し、手動測定との比較で検証しており、フェノタイピング手法が研究の中心です。
abstractwe have developed MyROOT, a novel software for the semi-automatic quantification of root growth of seedlings growing directly in agar plates.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicMyROOT software is available at https://www.cragenomica.es/research-Open asset ↗pdf-page:3 lines:1-45Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
We explore a recent, innovative variation of closed-system respirometry for terrestrial organisms, whereby oxygen partial pressure ( P O 2 ) is repeatedly measured fluorometrically in a constant-volume chamber over multiple time points. We outline a protocol that aligns this technology with the broader literature on aerial respirometry, including the calculations required to accurately convert O 2 depletion to metabolic rate (MR). We identify a series of assumptions, and sources of error associated with this technique, including thresholds where O 2 depletion becomes limiting, that impart errors to the calculation and interpretation of MR. Using these adjusted calculations, we found that the resting MR of five species of angiosperm seeds ranged from 0.011 to 0.640 ml g -1 h -1 , consistent with published seed MR values. This innovative methodology greatly expands the lower size limit of terrestrial organisms that can be measured, and offers the potential for measuring MR changes over time as a result of physiological processes of the organism.
Why it matches plant phenotyping methods蛍光式閉鎖系呼吸測定法のプロトコル、計算補正、誤差要因を開発・検証し、植物種子の代謝率という生理形質を測定しているため、植物フェノタイピング手法が中心です。
abstractWe explore a recent, innovative variation of closed-system respirometry for terrestrial organisms, whereby oxygen partial pressure ( P O 2 ) is repeatedly measured fluorometrically in a constant-volume chamber over multiple time points.
Reproduction assets foundThe paper's authors developed an annotated R script (Script 1) that automates their metabolic-rate calculations from Q2 fluorometric respirometry data, and it is explicitly stated to be available in the journal's supplementary material, which is publicly accessible at the supplemental URL. The seed respirometry raw/repCode · publicThe R script is available in the
supplementary material, and is heavily annotated to provide
guidance to its use (Script 1).Open asset ↗pdf-raw-page:2 lines:1-110Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
We demonstrate that optical coherence tomography (OCT) is a plausible optical tool for in vivo detection of plant seeds and its morphological changes during growth. To investigate the direct impact of salt stress on seed germination, the experiment was conducted using Capsicum annuum seeds that were treated with different molar concentrations of NaCl. To determine the optimal concentration for the seed growth, the seeds were monitored for nine consecutive days. In vivo two-dimensional OCT images of the treated seeds were obtained and compared with the images of seeds that were grown using sterile distilled water. The obtained results confirm the feasibility of using OCT for the proposed application. Normalized depth profile analysis was utilized to support the conclusions.
Why it matches plant phenotyping methodsOCTを用いた種子の形態変化の非破壊・生体内モニタリング手法を開発・実証しており、植物表現型の取得方法が中心である。
abstractWe demonstrate that optical coherence tomography (OCT) is a plausible optical tool for in vivo detection of plant seeds and its morphological changes during growth.
Reproduction assets foundThe paper's supplementary material (Table S1) contains the paper-specific phenotyping measurements: seed weight and embryo thickness statistics for all NaCl-treated and control seed groups across the 9-day monitoring period, publicly available at the MDPI supplementary URL. No analysis code or image datasets are statedSupplement · publicugh Advanced Production Technology Development Program, funded by Ministry of Agriculture, Food and Rural Affairs (MAFRA) (No. 314031-3). Additionally, this study was also supported by the BK21 Plus project funded by the Ministry of Education, Korea (21A20131600011).
Supplementary Materials
The following are available online at http://www.mdpi.com/1424-8220/17/12/2887/s1 . Table S1, The average weight gain observed and the averaged embryo thickness values for each group, along with its standard deviation value and the maximum and minimum values of seeds in each group that was observed during the entire monitoring process.
Click here for additional data file.
Author Contributions
The experimeOpen asset ↗lines:63-81Code / dataset availability confirmedEurope PMC · checked 10 Sept 2026
BarleyLaboratory / benchtopMRI / PETRootMorphology / geometry measurementRoot system architecture
Background Root systems are highly plastic and adapt according to their soil environment. Studying the particular influence of soils on root development necessitates the adaptation and evaluation of imaging methods for multiple substrates. Non-invasive 3D root images in soil can be obtained using magnetic resonance imaging (MRI). Not all substrates, however, are suitable for MRI. Using barley as a model plant we investigated the achievable image quality and the suitability for root phenotyping of six commercially available natural soil substrates of commonly occurring soil textures. The results are compared with two artificially composed substrates previously documented for MRI root imaging. Results In five out of the eight tested substrates, barley lateral roots with diameters below 300 µm could still be resolved. In two other soils, only the thicker barley seminal roots were detectable. For these two substrates the minimal detectable root diameter was between 400 and 500 µm. Only one soil did not allow imaging of the roots with MRI. In the artificially composed substrates, soil moisture above 70% of the maximal water holding capacity (WHC max ) impeded root imaging. For the natural soil substrates, soil moisture had no effect on MRI root image quality in the investigated range of 50-80% WHC max . Conclusions Almost all tested natural soil substrates allowed for root imaging using MRI. Half of these substrates resulted in root images comparable to our current lab standard substrate, allowing root detection down to a diameter of 300 µm. These soils were used as supplied by the vendor and, in particular, removal of ferromagnetic particles was not necessary. With the characterization of different soils, investigations such as trait stability across substrates are now possible using noninvasive MRI.
Why it matches plant phenotyping methodsMRIによる土壌中の根の非侵襲的画像化について、異なる土壌基質への適用性と画像品質を評価し、根径の検出性能を検証しているため、植物フェノタイピング手法が中心である。
abstractStudying the particular influence of soils on root development necessitates the adaptation and evaluation of imaging methods for multiple substrates.
Reproduction assets foundThe authors state that the 3D MRI root images and excavated root images from this study are publicly available under a DOI (IPK repository), directly reproducing the paper's root phenotyping measurements.Dataset · public3D root images and excavated root images are available at: http://dx.doi.org/10.5447/IPK/2017/10 .Open asset ↗IPK · 10.5447/IPK/2017/10lines:196-230Code / dataset availability confirmedbioRxiv · Europe PMC · checked 14 Sept 2026
How complex developmental-genetic networks are translated into organs with specific 3D shapes remains an open question. This question is particularly challenging because the elaboration of specific shapes is in essence a question of mechanics. In plants, this means how the genetic circuitry affects the cell wall. The mechanical properties of the wall and their spatial variation are the key factors controlling morphogenesis in plants. However, these properties are difficult to measure and investigating their relation to genetic regulation is particularly challenging. To measure spatial variation of mechanical properties, one must determine the deformation of a tissue in response to a known force with cellular resolution. Here we present an automated confocal micro-extensometer (ACME), which greatly expands the scope of existing methods for measuring mechanical properties. Unlike classical extensometers, ACME is mounted on a confocal microscope and utilizes confocal images to compute the deformation of the tissue directly from biological markers, thus providing cellular scale information and improved accuracy. ACME is suitable for measuring the mechanical responses in live tissue. As a proof of concept we demonstrate that the plant hormone gibberellic acid induces a spatial gradient in mechanical properties along the length of the Arabidopsis hypocotyl.\n\nTerms
Why it matches plant phenotyping methods植物組織の力学的性質を細胞解像度で定量する自動共焦点マイクロ伸展計を開発し、画像から変形を抽出する方法を中心に実証しているため。
abstractHere we present an automated confocal micro-extensometer (ACME), which greatly expands the scope of existing methods for measuring mechanical properties.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicThe positioners are controlled by a SmarAct MCS3D (SmarAct GmbH) controller (Figure 1C,
label 15) accompanied by its software library, which in turn is controlled by custom-made software
(available here: https://github.com/ACME-Robinson/InstallPackage)Open asset ↗ACME-Robinson/InstallPackagepdf-page:14 lines:1-54Code / dataset availability confirmedEurope PMC · checked 10 Sept 2026
BarleyChickpeaWheatLaboratory / benchtopX-ray / CTRootMorphology / geometry measurementSegmentationRoot system architecture
The objective of this study was to develop a flexible and free image processing and analysis solution, based on the Public Domain ImageJ platform, for the segmentation and analysis of complex biological plant root systems in soil from x-ray tomography 3D images. Contrasting root architectures from wheat, barley and chickpea root systems were grown in soil and scanned using a high resolution micro-tomography system. A macro (Root1) was developed that reliably identified with good to high accuracy complex root systems (10% overestimation for chickpea, 1% underestimation for wheat, 8% underestimation for barley) and provided analysis of root length and angle. In-built flexibility allowed the user interaction to (a) amend any aspect of the macro to account for specific user preferences, and (b) take account of computational limitations of the platform. The platform is free, flexible and accurate in analysing root system metrics.
Why it matches plant phenotyping methods植物根系の3D画像から根長・根角度を抽出する画像解析ツールの開発と精度評価が研究の中心であるため。
abstractThe objective of this study was to develop a flexible and free image processing and analysis solution
Reproduction assets foundThe paper's μCT root image data and analysis files (including the Root1 macro workflow) are stated to be publicly deposited in a Harvard Dataverse dataset with an explicit DOI, directly supporting this paper's root phenotyping measurements and analysis.Dataset · publicAll files are available from the database https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/DXG4AH .Open asset ↗doi:10.7910/DVN/DXG4AHlines:45-53Code / dataset availability confirmedEurope PMC · OpenAlex · checked 14 Sept 2026
Background Growth is an important parameter to consider when studying the impact of treatments or mutations on plant physiology. Leaf area and growth rates can be estimated efficiently from images of plants, but the experiment setup, image analysis, and statistical evaluation can be laborious, often requiring substantial manual effort and programming skills. Results Here we present rosettR , a non-destructive and high-throughput phenotyping protocol for the measurement of total rosette area of seedlings grown in plates in sterile conditions. We demonstrate that our protocol can be used to accurately detect growth differences among different genotypes and in response to light regimes and osmotic stress. rosettR is implemented as a package for the statistical computing software R and provides easy to use functions to design an experiment, analyze the images, and generate reports on quality control as well as a final comparison across genotypes and applied treatments. Experiment procedures are included as part of the package documentation. Conclusions Using rosettR it is straight-forward to perform accurate, reproducible measurements of rosette area and relative growth rate with high-throughput using inexpensive equipment. Suitable applications include screening mutant populations for growth phenotypes visible at early growth stages and profiling different genotypes in a wide variety of treatments.
Why it matches plant phenotyping methods植物ロゼット面積と成長率を画像から高スループットに測定するプロトコルおよびRソフトウェアの開発が研究の中心であり、再現性・精度も実証している。
abstractHere we present rosettR , a non-destructive and high-throughput phenotyping protocol for the measurement of total rosette area of seedlings grown in plates in sterile conditions.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicThe rosettR R-package along with example data is available from our github repository http://github.com/hredestig/rosettROpen asset ↗hredestig/rosettRlines:130-159Code / dataset availability confirmedEurope PMC · checked 15 Sept 2026
Published28 Feb 2017Cytometry. Part A : the journal of the International Society for Analytical CytologyCited by 5 · OpenAlex ↗
Why it matches plant phenotyping methods植物プロトプラスト画像から薬剤による表現型変化を自動検出する画像解析・統計パイプラインを開発し、ハイコンテントスクリーニングに適用しており、表現型取得・抽出法が中心です。
abstractQuantitative image analysis procedures are necessary for the automated discovery of effects of drug treatment in large collections of fluorescent micrographs.
Reproduction assets foundThe paper's AVAILABILITY section states that a Reproducible Research Archive containing all raw data (the Arabidopsis protoplast fluorescence microscopy images), software, and processed results is publicly available from the authors' mur-phylab URL, which appears in the allowed URL list.Code · publicsoftware, and processed results is available from http://mur-phylab.cbd.cmu.edu/software.ACKNOWLEDGMENTS
We thank Dr. Armaghan Naik for helpful discussions, Dr.
Roland Nitschke for advice on microscopy, and Katja Rapp
for technical support.
LITERATURE CITED
1. Giuliano KA, De Biasio RL, Dunlay RT, Gough A, Volosky JM, Zock J, Pavlakis GN,
Taylor DL. High-content screening: A new approach to easing key bottlenecks in the
drug discoOpen asset ↗http://mur-phylab.cbd.cmu.edu/software.ACKNOWLEDGMENTSpdf-raw-page:9 lines:94-155Code / dataset availability confirmedCrossref · checked 15 Sept 2026
Summary Spectroscopy has recently emerged as an effective method to accurately characterize leaf biochemistry in living tissue through the application of chemometric approaches to foliar optical data, but this approach has not been widely used for plant secondary metabolites. Here, we examine the ability of reflectance spectroscopy to quantify specific phenolic compounds in trembling aspen ( Populus tremuloides ) and paper birch ( Betula papyrifera ) that play influential roles in ecosystem functioning related to trophic‐level interactions and nutrient cycling. Spectral measurements on live aspen and birch leaves were collected, after which concentrations of condensed tannins (aspen and birch) and salicinoids (aspen only) were determined using standard analytical approaches in the laboratory. Predictive models were then constructed using jackknifed, partial least squares regression ( PLSR ). Model performance was evaluated using coefficient of determination ( R 2 ), root‐mean‐square error ( RMSE ) and the per cent RMSE of the data range (% RMSE ). Condensed tannins of aspen and birch were well predicted from both combined ( R 2 = 0·86, RMSE = 2·4, % RMSE = 7%)‐ and individual‐species models (aspen: R 2 = 0·86, RMSE = 2·4, % RMSE = 6%; birch: R 2 = 0·81, RMSE = 1·9, % RMSE = 10%). Aspen total salicinoids were better predicted than individual salicinoids (total: R 2 = 0·76, RMSE = 2·4, % RMSE = 8%; salicortin: R 2 = 0·57, RMSE = 1·9, % RMSE = 11%; tremulacin: R 2 = 0·72, RMSE = 1·1, % RMSE = 11%), and spectra collected from dry leaves produced better models for both aspen tannins ( R 2 = 0·92, RMSE = 1·7, % RMSE = 5%) and salicinoids ( R 2 = 0·84, RMSE = 1·4, % RMSE = 5%) compared with spectra from fresh leaves. The decline in prediction performance from total to individual salicinoids and from dry to fresh measurements was marginal, however, given the increase in detailed salicinoid information acquired and the time saved by avoiding drying and grinding leaf samples. Reflectance spectroscopy can successfully characterize specific secondary metabolites in living plant tissue and provide detailed information on individual compounds within a constituent group. The ability to simultaneously measure multiple plant traits is a powerful attribute of reflectance spectroscopy because of its potential for in situ – in vivo field deployment using portable spectrometers. The suite of traits currently estimable, however, needs to expand to include specific secondary metabolites that play influential roles in ecosystem functioning if we are to advance the integration of chemical, landscape and ecosystem ecology.
Why it matches plant phenotyping methods生葉の反射分光とPLSRにより二次代謝産物を定量する測定・予測手法を構築し、モデル性能を評価しており、植物形質取得法が研究の中心である。
abstractSpectroscopy has recently emerged as an effective method to accurately characterize leaf biochemistry in living tissue through the application of chemometric approaches to foliar optical data
Reproduction assets foundThe paper's Data Accessibility statement explicitly archives both the spectral data used in the study and the PLSR model-building code in EcoSIS, with a public URL matching an allowed URL.Dataset · publico PAT and RLL, and USDA NIFA McIntire-Stennis projects
WIS01651 to RLL and WIS01531 and WIS01599 to PAT.
Data Accessibility
Spectral data used in this study and the partial least squares regression code used for model
building are archived in the Ecosystem Spectral Information System (EcoSIS;
www.ecosis.org) and can be found at https://ecosis.org/#result/d5445eb9-f334-4ee7-90a9-1fe07e67a20c.Open asset ↗EcoSIS · d5445eb9-f334-4ee7-90a9-1fe07e67a20cpdf-raw-page:23 lines:1-25Code / dataset availability confirmedEurope PMC · checked 14 Sept 2026
Within the HarvestPlus program there are many collaborators currently using X-Ray Fluorescence (XRF) spectroscopy to measure Fe and Zn in their target crops. In India, five HarvestPlus wheat collaborators have laboratories that conduct this analysis and their throughput has increased significantly. The benefits of using XRF are its ease of use, minimal sample preparation and high throughput analysis. The lack of commercially available calibration standards has led to a need for alternative calibration arrangements for many of the instruments. Consequently, the majority of instruments have either been installed with an electronic transfer of an original grain calibration set developed by a preferred lab, or a locally supplied calibration. Unfortunately, neither of these methods has been entirely successful. The electronic transfer is unable to account for small variations between the instruments, whereas the use of a locally provided calibration set is heavily reliant on the accuracy of the reference analysis method, which is particularly difficult to achieve when analyzing low levels of micronutrient. Consequently, we have developed a calibration method that uses non-matrix matched glass disks. Here we present the validation of this method and show this calibration approach can improve the reproducibility and accuracy of whole grain wheat analysis on 5 different XRF instruments across the HarvestPlus breeding program.
Why it matches plant phenotyping methods小麦粒のFe・Zn濃度という植物形質を測定するXRF校正法を開発し、5台の装置で再現性と精度を検証しており、測定法が中心的です。
abstractConsequently, we have developed a calibration method that uses non-matrix matched glass disks.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Supplement · publicSupplementary material
The Supplementary Material for this article can be found online at: http://journal.frontiersin.org/article/10.3389/fpls.2016.00784
Click here for additional data file.Open asset ↗lines:369-504Code / dataset availability confirmedOpenAlex · Crossref · Europe PMC · checked 14 Sept 2026
Precise measurements of root system architecture traits are an important requirement for plant phenotyping. Most of the current methods for analyzing root growth require either artificial growing conditions (e.g. hydroponics), are severely restricted in the fraction of roots detectable (e.g. rhizotrons), or are destructive (e.g. soil coring). On the other hand, modalities such as magnetic resonance imaging (MRI) are noninvasive and allow high-quality three-dimensional imaging of roots in soil. Here, we present a plant root imaging and analysis pipeline using MRI together with an advanced image visualization and analysis software toolbox named NMRooting. Pots up to 117 mm in diameter and 800 mm in height can be measured with the 4.7 T MRI instrument used here. For 1.5 l pots (81 mm diameter, 300 mm high), a fully automated system was developed enabling measurement of up to 18 pots per day. The most important root traits that can be nondestructively monitored over time are root mass, length, diameter, tip number, and growth angles (in two-dimensional polar coordinates) and spatial distribution. Various validation measurements for these traits were performed, showing that roots down to a diameter range between 200 μm and 300 μm can be quantitatively measured. Root fresh weight correlates linearly with root mass determined by MRI. We demonstrate the capabilities of MRI and the dedicated imaging pipeline in experimental series performed on soil-grown maize (Zea mays) and barley (Hordeum vulgare) plants.
Why it matches plant phenotyping methodsMRIによる土壌中根系の3D画像取得・解析パイプラインと専用ソフトウェアを開発し、根形態形質を検証しており、植物フェノタイピング手法が研究の中心である。
abstractHere, we present a plant root imaging and analysis pipeline using MRI together with an advanced image visualization and analysis software toolbox named NMRooting.
Reproduction assets found保存済みの本文根拠を更新済みルールで再検証し、公開資産1件を確認しました。Code · publicAutomated image analysis was performed using an in-house developed software tool, named NMRooting (available at http://www.nmrooting.de ), which was written in the programming language PythonOpen asset ↗NMRootinglines:169-172