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Fast or slow - light climate modulates intra-population sinking velocities in small phytoplankton
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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.
Title: Fast or slow - light climate modulates intra-population sinking velocities in small phytoplankton
Description:
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.
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