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Fast or slow - light climate modulates intra-population sinking velocities in small phytoplankton

bioRxiv · 19 Jun 2025 · 10.1101/2025.06.13.659648

Abstract

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.

Plant phenotyping relevance

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
abstractOur well-plate microscopy approach using parallel imaging of many samples generates high-throughput measures of cell sinking at population- or community-scales

Code and data availability

The 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.

Codepublic

functional 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 16

Open resource ↗maxberthold/PhytoplanktonSinkVelocities · pdf-raw-page:8 lines:1-44

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