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Cell abundance

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Phytoplankton net growth rate (cell counting)
Approach: FCM or microscopy cell counts in time-course incubations
Context: incubation
Spatial scale: point sample
Temporal scale: hours
Units: d-1 (net growth rate)
Community captured: varies (FCM-resolvable populations or microscopy-counted taxa)
Co-measurements: (none specified)

Method Overview

Cell abundance is tracked over the course of incubation experiments using flow cytometry (FCM) or epifluorescence microscopy. The rate of change in cell concentration over time gives the net growth rate of the incubated population. When paired with dilution treatments (see Incubation dilution experiments), cell counting separates the contributions of growth and grazing to the net change in abundance. In the absence of dilution, the net growth rate (k = µ − g) is obtained directly; resolving µ and g requires an additional experimental manipulation.

Scale of measurement

Point samples after hours of incubation.

Data generated

Net phytoplankton growth rate (d-1) for each counted population. When combined with a dilution series, specific growth rate (µ) and grazing rate (g) are resolved.

Units & currency

Units are d-1. The currency is cells.

Sample size

Typical samples are < 1 L in volume.

Repositories & databases

Limitations

Cell counting alone gives the net rate (µ − g); resolving growth from grazing requires additional experimental manipulation (dilution, additions). FCM cannot distinguish living from recently dead cells, which can bias estimates.

Example Applications & Protocols

Classic examples

Recent applications

Common calculations/conversions

  • Net growth rate k (d-1) = ln(Nfinal/Ninitial) / t.

References