Abstract

The abundance and size distribution of plankton in the surface ocean are key metrics to understanding primary and export production, food web dynamics, and the optical properties of the water column. Here we quantified cell size and abundance of phytoplankton species from mono-specific laboratory cultures, using optical, electrical, and image-based benchtop instrumentation. Moreover, we combined particle size distribution and size fractionated chlorophyll a (Chl a) analysis with image analysis to estimate phytoplankton community composition and abundance comparing a high and low biomass station in the North Atlantic during springtime. In laboratory cultures, we found generally good agreement in estimates of both particle concentration and particle size among instruments. Image-based approaches (e.g. microscopy, FlowCam) delivered somewhat lower cell abundance estimates, because image-based instruments distinguish cells from non-living objects. Image-based approaches also measured 10-20% greater cell sizes, because measurements were based only on in-focus images of the target species. Particle counters delivered indistinguishable estimates of size and abundance with much lower effort and technical expertise required. Maximum coefficient of variation for cell abundance and size did not exceed 10 and 15% respectively. Measurement precision was consistent across instrument type and across the size spectrum from 3 to >40 µm equivalent spherical diameter. For whole plankton community analysis from the North Atlantic, combined estimation of Chl a concentration and image-based diversity assessments resolved the dominant contributing phytoplankton species and spatial differences in the size structure of the plankton community. These results provide strong support for using particle counters, that can rapidly process large volumes of samples, to quantify particle size and abundance, including rarer, larger particles. Species identities and community composition can be revealed by supplemental, image-based approaches. Application of this coupled approach can help identify fundamental ecosystem characteristics such as particle size spectra that affect primary production, trophic transfer and export. Ultimately, the tremendous species diversity of plankton can be leveraged as particle tracking and identification keys, such as near-real time identification of coherent water masses.

Highlights

  • The abundance and size distribution of particles in the surface ocean, including plankton, are critical determinants of the optical properties of aquatic primary and export production, food web structure, and biogeochemistry (Reynolds et al, 2010; Maranon, 2015)

  • Instrument software provides analysis tools, but these tools are often user selected and not always supported by establishment of a standard operating procedure. To address these challenges and establish particle characterization tools for the quantification of plankton, we present an instrument inter-comparison by evaluating measurements of cell abundance and cell size, along with reproducible, operator-independent analysis protocols that minimize user-induced biases in selection of the size ranges or particle types to include in analyses

  • These species were chosen because they represent a size range from pico- to microplankton and vary in their surface properties, including thecate dinoflagellates covered by cellulose plates

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Summary

Introduction

The abundance and size distribution of particles in the surface ocean, including plankton, are critical determinants of the optical properties of aquatic primary and export production, food web structure, and biogeochemistry (Reynolds et al, 2010; Maranon, 2015). Many phytoplankton have complex shapes that are difficult to express in simple geometric terms, yet size and shape of particles are key properties that affect light absorption and scattering, which are important metrics for satellite measurements and remote sensing of ocean ecosystem properties (Kostadinov et al, 2009; Mouw and Yoder, 2010). This problem is exacerbated by the diverse, taxon-specific cell surface coverings characteristic of phytoplankton (e.g., silica frustules, coccoliths)

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