Abstract:Because cold‐water diatoms’ baseline elemental density (BED) is substantially higher than temperate diatoms, previous polar studies may have underestimated diatoms’ contribution to elemental standing stocks, contribution to particulate organic carbon (POC) export and incorrectly modeled their susceptibility to future warming. We apply cold‐water diatom allometry to Arctic field samples and derive diatom growth rates ranging from 0.01–0.68 day−1, versus unrealistically high rates estimated using temperate diato… Show more
“…Such shifts in species composition influence community phytoplankton growth rates since the functional growth response to temperature in diatoms are almost three times that of dinoflagellates (Kremer et al., 2017). Cold water diatoms may respond even faster to enhanced temperature (Krause & Lomas, 2020). Smaller phytoplankton cells generally flourish in warmer and more stratified, low‐nutrient waters (Irwin et al., 2006).…”
Ocean primary production plays a major role in the global carbon cycle, accounting for about half of the world's carbon fixation (Falkowski et al., 1998). Primary production rates vary with temperature, nutrient, and light conditions (Bouman et al., 2018;Moore et al., 2013), and influence biogeochemical cycles and marine ecosystem productivity (Falkowski et al., 1998). Measures of gross primary production (GPP), net primary production (NPP), and net community production (NCP) rates, and phytoplankton community growth rates ( 𝐴𝐴 𝐴𝐴 𝑏𝑏 opt , i.e., the normalized primary production rates relative to chlorophyll-a, Chl-a) provide key metrics for assessing the fate of energy production by phytoplankton, energy availability to heterotrophs (e.g., bacteria, zooplankton, and fish) and the amount of organic carbon available for export (Cassar et al., 2015;Stanley et al., 2010). GPP is the amount of energy produced by primary producers (e.g., phytoplankton, ice algae) during a given time. NPP is the
“…Such shifts in species composition influence community phytoplankton growth rates since the functional growth response to temperature in diatoms are almost three times that of dinoflagellates (Kremer et al., 2017). Cold water diatoms may respond even faster to enhanced temperature (Krause & Lomas, 2020). Smaller phytoplankton cells generally flourish in warmer and more stratified, low‐nutrient waters (Irwin et al., 2006).…”
Ocean primary production plays a major role in the global carbon cycle, accounting for about half of the world's carbon fixation (Falkowski et al., 1998). Primary production rates vary with temperature, nutrient, and light conditions (Bouman et al., 2018;Moore et al., 2013), and influence biogeochemical cycles and marine ecosystem productivity (Falkowski et al., 1998). Measures of gross primary production (GPP), net primary production (NPP), and net community production (NCP) rates, and phytoplankton community growth rates ( 𝐴𝐴 𝐴𝐴 𝑏𝑏 opt , i.e., the normalized primary production rates relative to chlorophyll-a, Chl-a) provide key metrics for assessing the fate of energy production by phytoplankton, energy availability to heterotrophs (e.g., bacteria, zooplankton, and fish) and the amount of organic carbon available for export (Cassar et al., 2015;Stanley et al., 2010). GPP is the amount of energy produced by primary producers (e.g., phytoplankton, ice algae) during a given time. NPP is the
“…As an example, Lomas et al (2019) and Krause and Lomas (2020) both used the FlowCam automated biovolume (cylinder) measure to represent biovolume of mixed diatom samples when proposing and validating a new method for calculating cold‐water diatom elemental density, an important measure used to reflect diatom standing stocks and carbon flux, and for predicting the influences of climate change. Lomas et al (2019) present the new cold‐water diatom allometry calculation based on FlowCam biovolume (cylinder) outputs, while Krause and Lomas (2020) test the calculation on additional FlowCam biovolume (cylinder) outputs and then also compare these findings to those of several prior studies (not using FlowCam) that relied on existing temperate diatom allometry calculations, concluding that the new method is different (with diatom contributions significantly increased) but superior. We have shown (in Case Study 3) that this FlowCam output is calculated incorrectly and produces either over‐ or under‐estimates of biovolume depending on diatom orientation.…”
Section: Discussionmentioning
confidence: 99%
“…We have shown (in Case Study 3) that this FlowCam output is calculated incorrectly and produces either over‐ or under‐estimates of biovolume depending on diatom orientation. Lomas et al (2019) do not describe any FlowCam image sorting, while Krause and Lomas (2020) specifically state that images were manually sorted to exclude empty frustules, but do not mention cell orientation. Lomas et al (2019) state that their FlowCam biovolume (cylinder) estimates compared favorably to manual microscopic quantification (no data are provided), but we know that this measure is incorrect, especially for unsorted cell orientations.…”
Section: Discussionmentioning
confidence: 99%
“…These examples clearly highlight that due to the complexities of calculating measures based on two-dimensional images, automated outputs can exhibit marked errors. Given this finding, the veracity of the 10 studies that used FlowCam geodesic length, geodesic width or biovolume (cylinder) outputs is brought into question, especially where those findings were compared to previous data collected using traditional manual microscopy techniques (Krause and Lomas 2020). It is vital that researchers carefully consider which automated outputs they make use of and take the time to check that they accurately represent the features they are estimating for their specific cells.…”
Accurate and detailed reporting of methods is essential for scientific progress, yet it is widely accepted that authors across all scientific fields tend to provide insufficient methods detail. Given the recent proliferation of automated and semi‐automated technologies for data collection, to address this widespread issue the details needed for interpretation and reproducibility for each specific technique first need to be identified. A systematic literature review assessed the comprehensiveness of method details reported by 116 peer‐reviewed studies published between 2017 and 2020 using the FlowCam (a widely used imaging flow cytometer) to image phytoplankton, finding all to be lacking in critical details, inhibiting reproducibility, and limiting the veracity of some findings. Through this review and three case studies, we identify several key method details that should be reported by FlowCam studies to ensure their findings are credible, comparable, and replicable and illustrate the wide‐reaching implications for not doing so. Future studies using FlowCam for phytoplankton analyses should ensure clear reporting of all relevant details relating to the FlowCam unit, sample preparation, run settings, post‐processing of images, and the considered use of only verified measurement outputs. A methods reporting template is presented as a guideline intended to enhance the quality, interpretability, and repeatability of future FlowCam papers. The pervasiveness of inadequacies in FlowCam methods reporting identified here highlights how vital it is for users of any automated or semi‐automated scientific technologies to have a clear understanding of the impact of all method details on their findings, and to report these details adequately.
“…Due to their high sinking rates, diatoms have the capacity to transfer organic carbon (OC) and biogenic silicon (bioSi) from the productive surface layer to the deep ocean. As a result, diatoms are widely identified as the most relevant phytoplankton group for unraveling SO organic carbon cycling (Bathmann et al, 1991;Smetacek et al, 2012;Krause and Lomas, 2020). To fully understand diatom-driven export, and hence how carbon and silicon are sequestered, it is also critical to consider diatom ecological traits.…”
Physical and biogeochemical processes in the Southern Ocean are fundamental for modulating global climate. In this context, a process-based understanding of how Antarctic diatoms control primary production and carbon export, and hence global-ocean carbon sequestration, has been identified as a scientific priority. Here we use novel sediment trap observations in combination with a data-assimilative ocean biogeochemistry model (ECCO-Darwin) to understand how environmental conditions trigger diatom ecology in the iron-fertilized southern Scotia Sea. We unravel the role of diatoms assemblage in controlling the biogeochemistry of sinking material escaping from the euphotic zone, and discuss the link between changes in upper-ocean environmental conditions and the composition of settling material exported from the surface to 1,000 m depth from March 2012 to January 2013. The combined analysis of in situ observations and model simulation suggests that an anomalous sea-ice episode in early summer 2012–2013 favored (via restratification due to sea-ice melt) an early massive bloom of Corethron pennatum that rapidly sank to depth. This event drove high biogenic silicon to organic carbon export ratios, while modulating the carbon and nitrogen isotopic signals of sinking organic matter reaching the deep ocean. Our findings highlight the role of diatom ecology in modulating silicon vs. carbon sequestration efficiency, a critical factor for determining the stoichiometric relationship of limiting nutrients in the Southern Ocean.
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