Andrew D. Barton’s research while affiliated with University of California, San Diego and other places

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Publications (53)


Geographic location and characterization of sampling sites. (a) General overview of the geographic location, circles represent detailed spatial location of samples collected from the Salton Sea. Sampling dates are indicated by color: white = 15 January 2019 (n = 6), orange = 30 January 2019 (n = 2), pink = 17 May 2019 (n = 11), red = 27 June 2019 (n = 1), and purple = 10 July 2019 (n = 1). Inset (red rectangle) in (a) shows the location of the sampling area in (b) where (c) Environmental water samples in light blue circles and (d) Soil samples in brown circles were collected at each environment. Inset (blue rectangle) in (b) shows the sampling area inside Viridos facility in (e) where aerosol (in orange) and open colonizing tanks (in green) samples were collected. Open colonizing tanks were located in concentric rings 100 m, 200 m, 365 m, and 550 m apart. Geographic maps in (a–d) were obtained from Google Maps and (e) was obtained from Google Earth Pro.
Analysis of the richness and diversity of each environment type. (a) Venn diagram of shared and unique ASV numbers among samples. Shannon diversity of bacterial (b) and eukaryotic ASVs (c) by environment, respectively. Letters A, B, and C in (b) and (c) denote statistically significant differences (ANOVA; Tukey’s HSD Test P < 0.05) in Shannon’s diversity values among the compared environments.
Bacterial community characterization by environment type. (a) Radar plots of most abundant taxonomic groups. Groups further from the center have higher relative abundances. Only taxonomic groups above 10% relative abundance are shown. Bacterial PCoA based on (b) taxonomic composition at the ASV level. (c) Madin et al. (21) phenotypic trait database and (d) FAPROTAX functional trait database. Arrows length for cell length in (c) and aerobic chemoheterotrophy and cyano/chloroplast in (d) were reduced by a factor of 10 to help visualize all arrows on one graph. Only the top 10 ASVs are shown on the ordination in (b) represented by letters: A, J: Cyanobacteria; Family IX; GpIX, B: Cyanobacteria; Family X; GpX, C: Alphaproteobacteria; Rhodobacterales; Roseivivax, D: Actinobacteria; Actinomycetales; Corynebacterium, E: Firmicutes; Bacillales; Salinicoccus, F: Betaproteobacteria; Burkholderiales; Variovorax, G: Actinobacteria; Actinomycetales; Kocuria, H: Bacteroidetes; Sphingobacteriales; Gracilimonas, I: Alphaproteobacteria; SAR11; Candidatus Pelagibacter. Letter D is located behind E on the plot. Results from PERMANOVA (function “adonis”) statistical test in (b–d) are: Pseudo F-ratio, their associated P-value, and the R². Aer chemoHT, aerobic chemoheterotrophy; cyano/chloro, cyanobacteria/chloroplast; dia, diameter; Ferment, fermentation; HC degrad, hydrocarbon degradation; Mesoph, mesophilic; PHt, photoheterotrophy; PT, phototrophy; Spor, Sporulation; tol, tolerant.
Eukaryote community characterization by environment type. (a) Radar plots of most abundant taxonomic groups. Groups further from the center have higher relative abundances. Only taxonomic groups above 10% relative abundance are shown. PCoA based on (b) taxa composition at the ASV level and (c) phenotypic traits. Results from PERMANOVA (function “adonis”) statistical test in (b and c) are Pseudo F-ratio, their associated P-value, and the R². At, autotrophy; Col, colony forming; Fla, flagella; Ht, Heterotrophy; Micro, micro size; Nano, nano size; Nk, naked cover; Org, organic cover; Si, siliceous cover; Swim, swimmer.
Examples of phenotypic traits that differed by environment types for (a) bacteria and (b) eukaryotes. Letters A, B, C, and D denote statistically significant differences among environments (ANOVA; Tukey’s HSD Test P < 0.05). For each of the microbial communities, black circles represent samples, and red dots represent the mean. In (a), the y axis represents abundance-weighted averages of a trait in each of the samples; this is accounting for the trait value multiplied by its relative abundance; in (b), the y axis represents relative abundances of that trait in each of the samples.

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Traits determine dispersal and colonization abilities of microbes
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February 2025

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Many microbes disperse through the air, yet the phenotypic traits that enhance or constrain aerial dispersal or allow successful colonization of new habitats are poorly understood. We used a metabarcoding bacterial and eukaryotic data set to explore the trait structures of the aquatic, terrestrial, and airborne microbial communities near the Salton Sea, California, as well as those colonizing a series of experimental aquatic mesocosms. We assigned taxonomic identities to amplicon sequence variants (ASVs) and matched them to functional trait values through published papers and databases that infer phenotypic and/or metabolic traits information from taxonomy. We asked what traits distinguish successful microbial dispersers and/or colonizers from terrestrial and aquatic source communities. Our study found broad differences in taxonomic and trait composition between dispersers and colonizers compared to the source soil and water communities. Dispersers were characterized by larger cell diameters, colony formation, and fermentation abilities, while colonizers tended to be phototrophs that form mucilage and have siliceous coverings. Shorter population doubling times, spore-, and/or cyst-forming organisms were more abundant among the dispersers and colonizers than the sources. These results show that the capacity for aerial dispersal and colonization varies among microbial functional groups and taxa and is related to traits that affect other functions like resource acquisition, predator avoidance, and reproduction. The ability to disperse and colonize new habitats may therefore distinguish microbial guilds based on tradeoffs among alternate ecological strategies. IMPORTANCE Microbes have long been thought to disperse rapidly across biogeographic barriers; however, whether dispersal or colonization vary among taxa or groups or is related to cellular traits remains unknown. We use a novel approach to understand how microorganisms disperse and establish themselves in different environments by looking at their traits (physiology, morphology, life history, and behavior characteristics). By collecting samples from habitats including water, soil, and the air and colonizing experimental tanks, we found dispersal and invasion vary among microorganisms. Some taxa and functional groups are found more often in the air or colonizing aquatic environments, while others that are commonly found in the soil or water rarely disperse or invade new habitat. Interestingly, the traits that help microorganisms survive and thrive also play a role in their ability to disperse and colonize. These findings have significant implications for understanding microorganisms’ success and adaptation to new environments.

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Temporal dynamics and distributions of sardine and anchovy in the southern California Current Ecosystem

January 2025

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246 Reads

Anchovies and sardines are some of the most economically and ecologically important and well-studied fishes on Earth, but there is still uncertainty regarding how distributions and abundances change through time and space. We bring together larval abundance data for northern anchovy (Engraulis mordax) and Pacific sardine (Sardinops sagax) collected by United States and Mexican scientists over 50 years (1963–2015) to test the Basin and Asynchrony hypotheses. The Basin hypothesis states that a species’ geographic range and spawning area (R) increase with overall abundance (A) according to a power law, R = aAb , where the exponent (b) is less than ∼0.5 when the rate of increasing area occupied saturates as population size increases. The Asynchrony hypothesis postulates that anchovy and sardine abundances are negatively correlated through time. We found that the Basin hypothesis was supported for both species but the Asynchrony hypothesis was not during this 53-year period. Due to collaboration between US and Mexican scientists, we were able to better understand how two important fishes utilize their environment.


Changes in Arctic Ocean plankton community structure and trophic dynamics on seasonal to interannual timescales

November 2024

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203 Reads

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2 Citations

The Arctic Ocean experiences significant seasonal to interannual environmental changes, including in temperature, light, sea ice, and surface nutrient concentrations, that influence the dynamics of marine plankton populations. Here, we use a hindcast simulation (1948–2009) of size-structured Arctic Ocean plankton communities, ocean circulation, and biogeochemical cycles in order to better understand how seasonal to interannual changes in the environment influence phytoplankton physiology, plankton community structure, trophic dynamics, and fish production in the Arctic Ocean. The growth of model phytoplankton was primarily limited in winter, spring, and fall by light, but in summer, the growth of smaller and larger phytoplankton was mostly limited by temperature and nutrient availability, respectively. The dominant trophic pathway in summer was from phytoplankton to herbivorous zooplankton such that the average trophic position of model zooplankton was lower in the summer growing season compared to the rest of the year. On interannual timescales, changes in plankton community composition were strongly tied to interannual changes in bottom-up forcing by the environment. In the summer, in years with less ice and warmer temperatures, the biomass of phytoplankton and zooplankton was higher, the size–abundance relationship slopes were more negative (indicative of a phytoplankton community enriched in smaller phytoplankton), zooplankton had higher mean trophic position (indicative of greater carnivory), and potential fishery production was greater, fueled by increased mesozooplankton biomass and flux of organic matter to the benthos. The summertime shift toward greater carnivory in warmer and low-ice years was due primarily to changes in phenology, with phytoplankton and microzooplankton blooms occurring approximately 1 month earlier in these conditions and carnivorous zooplankton increasing in abundance during summer. The model provides a spatially and temporally complete overview of simulated changes in plankton communities in the Arctic Ocean occurring on seasonal to interannual timescales, and it provides insights into the mechanisms underlying these changes as well as their broader biogeochemical and ecosystem significance.


Relationships between phytoplankton pigments and DNA- or RNA-based abundances support ecological applications

November 2024

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206 Reads

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1 Citation

Observations of phytoplankton abundances and community structure are critical towards understanding marine ecosystems. Common approaches to determine group-specific abundances include measuring phytoplankton pigments via high-performance liquid chromatography and DNA-based metabarcoding. Increasingly, mRNA abundances via metatranscriptomics are also employed. As phytoplankton pigments are used to develop and validate remote sensing algorithms, further comparisons between pigments and other metrics are needed to validate the extent to which these measurements agree for group-specific abundances; however, most previous comparisons have been hindered by metabarcoding and metatranscriptomics solely producing relative abundance data. By employing quantitative approaches that express both 18S rDNA and total mRNA as concentrations, we show that these measurements are related for several eukaryotic phytoplankton groups. We further propose that integration of these can be used to examine ecological patterns more deeply. For example, productivity-diversity relationships of both the whole community and individual groups show a dinoflagellate-driven negative trend rather than the commonly-found unimodal pattern. Pigments are also shown to relate to certain harmful algal bloom-forming taxa as well as the expression of sets of genes. Altogether, these results suggest that potential models of pigment concentrations via hyperspectral remote sensing may enable improved assessments of global phytoplankton community structure, including the detection of harmful algal blooms, and support the development of ecosystem models.


Description of the sampling regime and environment over 2014–2020. (a) Total number of samples per station. Squares highlight cardinal stations which are sampled every cruise. (b) Mean temperature (°C), (c) salinity (PSU), (d) and NO3 + NH3, µM per station across all cruises.
Rank curves for 16S, 18S-V4, and 18S-V9. (a) log10–log10 relationship between mean abundance (reads) and abundance rank. (b) log10–log10 relationship between mean occurrence (samples) and occurrence rank. (c) log10–log10 relationship between mean occurrence (stations) and occurrence rank. Color indicates either 16S (pink), 18S-V4 (green), or 18S-V9 (blue) ASVs. Shading around the means (points) show the upper (95%) and lower (5%) percentiles of either abundance or occurrence, calculated from the 1000-member rarefaction ensemble. ASVs that were observed with an average of < 1 read, sample, or station were removed from these figures for improved clarity.
(a) Temperature, salinity, and dissolved inorganic nitrogen (NO3 + NH3) for the 445 samples used in this study. Axes show temperature (°C) and salinity (PSU). The size of the points represents NO3 + NH3 (µM) of each sample. Color of the points represents the identified SOM clusters which align with known water masses: Pacific Subarctic Upper Water (PSUW, blue), East North Pacific Central Water (ENPCW, green), and Pacific Equatorial Water (PEW, orange). Solid grey lines indicate isopycnals of constant seawater density (c,d). (b) Map showing the most dominant water mass per station (color of circles), where the size of the circles represents the frequency with which that water mass is observed at a given station. (c,d) Example temperature and salinity diagram showing the occurrence and relative abundance of an endemic (Flavobacteriaceae spp.) and cosmopolitan (Synechococcus sp. CC9902) ASV, respectively, across all 445 samples. The color of the points represents the relative abundance of the ASV per sample. Blue, green, and orange shaded regions show the boundary of each water mass/pelagic habitat. The size of the points represents NO3 + NH3 (µM) of each sample. (e,f) Example significance vs abundance diagrams for the endemic and cosmopolitan ASVs in (c,d), highlighting which pelagic habitats the ASVs had a significant affinity for (p-value < 0.05, dashed line). The x-axis shows the mean relative abundance within a pelagic habitat—the overall (across all samples) mean relative abundance for that ASV. The y-axis shows the p-value associated with each mean relative abundance per pelagic habitat (see “Methods” section for p-value calculation). A high value along the x-axis means that the abundance within a pelagic habitat is higher than the mean overall abundance for that taxon across all samples. Values below the dashed line on the y-axis represent ensemble members where the abundance was significantly greater in a pelagic habitat then the null (p-value < 0.05). Thus, in this example, the endemic ASV is significantly overabundant in the pelagic habitat it is observed in (PEW), while the cosmopolitan species, while found everywhere, is only significantly overabundant in the PEW.
(a–c) Percentage of 16S, 18S-V9, and 18S-V4 ASVs respectively, in each biogeographic category (Endemic, Generalist, and Cosmopolitan). Values above each bar show the number of ASVs in each category. (d–f) Percentage of 16S, 18S-V9, and 18S-V4 ASVs respectively, in each affinity (zero habitat affinities, one habitat affinity, or two habitat affinities). Values above each bar show the number of ASVs in each biogeographic category. (g–i) Percentage of 16S, 18S-V9, and 18S-V4 ASVs respectively, in each habitat affinity level per biogeographic category. (j–l) Distributions of mean overall (across all samples) relative abundance across all 16S, 18S-V9, and 18S-V4 ASVs respectively. Distributions are separated per descriptive category and affinity level. Shades of gray in (g–i) correspond to the shades of gray for habitat affinities used in (d–f).
(a,b) Taxonomic overlap between NCOG and BioGEOTRACES, Tara Oceans, and Tara Polar for 16S (a) and Tara Oceans and Tara Polar for 18S-V9 (b). Size of circles indicates the mean number of ASVs identified per region per database. Edge color represents the database for the respective data (NCOG, BioGEOTRACES, Tara Ocean, or Tara Polar). Fill color represents the percentage of NCOG ASVs found in each respective region/dataset. (c,d) Relationship between regional richness (per database) and the % overlap between NCOG 16S ASVs and regional 16S and 18S-V9 ASVs. Each point represents a different region, as seen in (a,b). Colors represent the three biogeographic categories (Endemic, Generalist, Cosmopolitan). Linear fits between region-database richness and percent overlap were derived from the glm package in R.
Endemic, cosmopolitan, and generalist taxa and their habitat affinities within a coastal marine microbiome

September 2024

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114 Reads

The relative prevalence of endemic and cosmopolitan biogeographic ranges in marine microbes, and the factors that shape these patterns, are not well known. Using prokaryotic and eukaryotic amplicon sequence data spanning 445 near-surface samples in the Southern California Current region from 2014 to 2020, we quantified the proportion of taxa exhibiting endemic, cosmopolitan, and generalist distributions in this region. Using in-situ data on temperature, salinity, and nitrogen, we categorized oceanic habitats that were internally consistent but whose location varied over time. In this context, we defined cosmopolitan taxa as those that appeared in all regional habitats and endemics as taxa that only appeared in one habitat. Generalists were defined as taxa occupying more than one but not all habitats. We also quantified each taxon’s habitat affinity, defined as habitats where taxa were significantly more abundant than expected. Approximately 20% of taxa exhibited endemic ranges, while around 30% exhibited cosmopolitan ranges. Most microbial taxa (50.3%) were generalists. Many of these taxa had no habitat affinity (> 70%) and were relatively rare. Our results for this region show that, like terrestrial systems and for metazoans, cosmopolitan and endemic biogeographies are common, but with the addition of a large number of taxa that are rare and randomly distributed.


Changes in Arctic Ocean plankton community structure and trophic dynamics on seasonal to interannual timescales

May 2024

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62 Reads

The Arctic Ocean experiences significant seasonal to interannual environmental changes, including in temperature, light, sea ice, and surface nutrient concentrations, that influence the dynamics of marine plankton populations. Here, we use a hindcast simulation (1948–2009) of size-structured Arctic Ocean plankton communities, ocean circulation, and biogeochemical cycles in order to better understand how seasonal to interannual changes in the environment influence phytoplankton physiology, plankton community structure, trophic dynamics, and fish production in the Arctic Ocean. The growth of model phytoplankton was primarily limited in winter, spring, and fall by light, but in summer, the growth of smaller and larger phytoplankton was mostly limited by temperature and nutrient availability, respectively. The dominant trophic pathway in summer was from phytoplankton to herbivorous zooplankton, such that the average trophic position of model zooplankton was lower in the summer growing season compared with the rest of the year. On interannual timescales, changes in plankton community composition were strongly tied to interannual changes in bottom-up forcing by the environment. In the summer, in years with lower ice and warmer temperatures, the biomass of phytoplankton and zooplankton was higher, the size abundance relationship slopes were more negative (indicative of a phytoplankton community enriched in smaller phytoplankton), zooplankton had higher mean trophic position (indicative of greater carnivory), and potential fisheries production was greater, fueled by increased mesozooplankton biomass and flux of organic matter to the benthos. The summertime shift toward greater carnivory in warmer and low-ice years was due primarily to changes in phenology, with phytoplankton and microzoopankton blooms occurring approximately one month earlier in these conditions, and carnivorous zooplankton increasing in abundance during summer. The model provides a spatially and temporally complete overview of changes in plankton communities in the Arctic Ocean occurring on seasonal to interannual timescales, and provides insights on the mechanisms underlying these changes as well as their broader biogeochemical and ecosystems significance.


The XSO framework (v0.1) and Phydra library (v0.1) for a flexible, reproducible, and integrated plankton community modeling environment in Python

February 2024

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92 Reads

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1 Citation

Plankton community modeling is a critical tool for understanding the processes that shape marine ecosystems and their impacts on global biogeochemical cycles. These models can be of variable ecological, physiological, and physical complexity. Many published models are either not publicly available or implemented in static and inflexible code, thus hampering adoption, collaboration, and reproducibility of results. Here we present Phydra, an open-source library for plankton community modeling, and Xarray-simlab-ODE (XSO), a modular framework for efficient, flexible, and reproducible model development based on ordinary differential equations. Both tools are written in Python. Phydra provides pre-built models and model components that can be modified and assembled to develop plankton community models of various levels of ecological complexity. The components can be created, adapted, and modified using standard variable types provided by the XSO framework. XSO is embedded in the Python scientific ecosystem and is integrated with tools for data analysis and visualization. To demonstrate the range of applicability and how Phydra and XSO can be used to develop and execute models, we present three applications: (1) a highly simplified nutrient–phytoplankton (NP) model in a chemostat setting, (2) a nutrient–phytoplankton–zooplankton–detritus (NPZD) model in a zero-dimensional pelagic ocean setting, and (3) a size-structured plankton community model that resolves 50 phytoplankton and 50 zooplankton size classes with functional traits determined by allometric relationships. The applications presented here are available as interactive Jupyter notebooks and can be used by the scientific community to build, modify, and run plankton community models based on differential equations for a diverse range of scientific pursuits.


Figure 9b). The species in our model did, however, have realized niche optima that were, on average, slightly colder than the fundamental temperature niche optimums (í µí»¿ T opt < 0; Figure 9b). Previous studies (Kingsolver et al., 2013; Smith et al., 2021) have observed this pattern across a range of organisms. Fundamental temperature niches are typically, and in this model, assumed to have a left-or negativelyskewed curve where growth above the optimum temperature
Effects of dispersal and temperature variability on phytoplankton realized temperature niches

February 2024

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55 Reads

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1 Citation

Phytoplankton species exhibit fundamental temperature niches that drive observed species distributions linked to realized temperature niches. A recent analysis of field observations of Prochlorococcus showed that for all ecotypes, the realized niche was, on average, colder and wider than the fundamental niche. Using a simple trait‐based metacommunity model that resolves fundamental temperature niches for a range of competing phytoplankton, we ask how dispersal and local temperature variability influence species distributions and diversity, and whether these processes help explain the observed discrepancies between fundamental and realized niches for Prochlorococcus . We find that, independently, both dispersal and temperature variability increase realized temperature niche widths and local diversity. The combined effects result in high diversity and realized temperature niches that are consistently wider than fundamental temperature niches. These results have broad implications for understanding the drivers of phytoplankton biogeography as well as for refining species distribution models used to project how climate change impacts phytoplankton distributions.


Phytoplankton thermal trait parameterization alters community structure and biogeochemical processes in a modeled ocean

December 2023

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167 Reads

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5 Citations

Phytoplankton exhibit diverse physiological responses to temperature which influence their fitness in the environment and consequently alter their community structure. Here, we explored the sensitivity of phytoplankton community structure to thermal response parameterization in a modelled marine phytoplankton community. Using published empirical data, we evaluated the maximum thermal growth rates (μmax) and temperature coefficients (Q10; the rate at which growth scales with temperature) of six key Phytoplankton Functional Types (PFTs): coccolithophores, cyanobacteria, diatoms, diazotrophs, dinoflagellates, and green algae. Following three well‐documented methods, PFTs were either assumed to have (1) the same μmax and the same Q10 (as in to Eppley, 1972), (2) a unique μmax but the same Q10 (similar to Kremer et al., 2017), or (3) a unique μmax and a unique Q10 (following Anderson et al., 2021). These trait values were then implemented within the Massachusetts Institute of Technology biogeochemistry and ecosystem model (called Darwin) for each PFT under a control and climate change scenario. Our results suggest that applying a μmax and Q10 universally across PFTs (as in Eppley, 1972) leads to unrealistic phytoplankton communities, which lack diatoms globally. Additionally, we find that accounting for differences in the Q10 between PFTs can significantly impact each PFT's competitive ability, especially at high latitudes, leading to altered modeled phytoplankton community structures in our control and climate change simulations. This then impacts estimates of biogeochemical processes, with, for example, estimates of export production varying by ~10% in the Southern Ocean depending on the parameterization. Our results indicate that the diversity of thermal response traits in phytoplankton not only shape community composition in the historical and future, warmer ocean, but that these traits have significant feedbacks on global biogeochemical cycles.


Dinoflagellate vertical migration fuels an intense red tide

August 2023

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111 Reads

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17 Citations

Proceedings of the National Academy of Sciences

Harmful algal blooms (HABs) are increasing globally, causing economic, human health, and ecosystem harm. In spite of the frequent occurrence of HABs, the mechanisms responsible for their exceptionally high biomass remain imperfectly understood. A 50-y-old hypothesis posits that some dense blooms derive from dinoflagellate motility: organisms swim upward during the day to photosynthesize and downward at night to access deep nutrients. This allows dinoflagellates to outgrow their nonmotile competitors. We tested this hypothesis with in situ data from an autonomous, ocean-wave-powered vertical profiling system. We showed that the dinoflagellate Lingulodinium polyedra's vertical migration led to depletion of deep nitrate during a 2020 red tide HAB event. Downward migration began at dusk, with the maximum migration depth determined by local nitrate concentrations. Losses of nitrate at depth were balanced by proportional increases in phytoplankton chlorophyll concentrations and suspended particle load, conclusively linking vertical migration to the access and assimilation of deep nitrate in the ocean environment. Vertical migration during the red tide created anomalous biogeochemical conditions compared to 70 y of climatological data, demonstrating the capacity of these events to temporarily reshape the coastal ocean's ecosystem and biogeochemistry. Advances in the understanding of the physiological, behavioral, and metabolic dynamics of HAB-forming organisms from cutting-edge observational techniques will improve our ability to forecast HABs and mitigate their consequences in the future.


Citations (39)


... Shifts in zooplankton species composition can reflect broader ecological disruptions, such as changes in predator populations, water quality, or habitat structure. For instance, a decline in copepod populations, which are a crucial food source for fish larvae, may foreshadow declines in higher trophic levels [54][55][56]. ...

Reference:

Final-The Unsung Heroes of Aquatic Ecosystems The Vital (2025-03-20 17 01 53)
Changes in Arctic Ocean plankton community structure and trophic dynamics on seasonal to interannual timescales

... In an iteration of the Community Earth Systems Model, pico-phytoplankton (0.2-2 μm) were found to contribute 58% to NPP [66]. While a DNA study across the North Pacific found that the 0.2-0.7 μm fraction of the CCE was dominated by chlorophytes and photosynthetic dinof lagellates [67]; both taxa taken together make up ∼25% of the community composition in our study (Fig. 3C), resulting in the low-end calculation of 43%. ...

Relationships between phytoplankton pigments and DNA- or RNA-based abundances support ecological applications

... By adopting the classic slab physics approximation (Fasham et al., 1990;Post et al., 2024), the modelled lake is subdivided into an upper well-mixed layer and a bottom nutrient-rich layer, with the boundary between them being defined by the variable depth of the upper mixed layer (henceforth the Mixed Layer Depth, MLD; Fig. 1). In most lake ecosystems, the exchange of biomass fluxes between the two layers is driven by physical processes. ...

The XSO framework (v0.1) and Phydra library (v0.1) for a flexible, reproducible, and integrated plankton community modeling environment in Python

... The growth of algae is influenced by WT, which impacts the speed of enzymatic reactions involved in their photosynthesis and respiration processes. The increase in WT will affect the photosynthesis and respiration of phytoplankton and then directly or indirectly affects the change in community structure [43]. At the appropriate temperature, an increase in water temperature can promote the rapid growth of algae [44]. ...

Effects of dispersal and temperature variability on phytoplankton realized temperature niches

... Two responsible processes were proposed by Franzè et al. (2023) to explain the low grazing pressure measured under warming and nutrient-enrichment conditions: changes in composition toward less palatable species (Anderson et al. 2022) and that μ were maximal. We found support for the explanation as the proportion of these species (mainly nanoplanktonic and microplanktonic chain-forming diatoms) was significantly higher under extreme compared to the control and moderate warming ($ 26 vs. ≤ 18; Anderson et al. 2024). By contrast, we did not observe any change in the contribution of picoplankton to the total community over time. ...

Phytoplankton thermal trait parameterization alters community structure and biogeochemical processes in a modeled ocean

... Here, we investigated how the microscale motility of snow algae, in response to light and temperature, may enable population movement and bloom formation in cold environments, as it does with phytoplankton in the formation of harmful algal blooms (13) or in enhancing oceanic primary production (14). However, snow algae occupy more extreme and dynamic terrestrial environments than their ocean counterparts, experience low temperatures with freeze-thaw cycles, snow cover, dark to very bright light levels, and often display complex life cycles including biciliate or "flagellate" motile stages as well as diverse non-motile cell morphologies (15)(16)(17)(18). ...

Dinoflagellate vertical migration fuels an intense red tide
  • Citing Article
  • August 2023

Proceedings of the National Academy of Sciences

... Quantifying the relative importance of each process in different regions of the global ocean is a challenging task due to the lack of observations that can fully resolve submesoscale dynamics. Recent advancements in Lagrangian analysis methods, which track changes in water properties along particle trajectories, have made progress in addressing this challenge 21 . By combining surface drifters, satellite ocean-color, and altimetry data, Zhang et al. (ref. ...

A Global Comparison of Marine Chlorophyll Variability Observed in Eulerian and Lagrangian Perspectives

... In addition, the FlowCam is well suited to analyzing live samples which may help to resolve several biases introduced by cell shrinkage and distortion associated with preservation for light microscopy (Zarauz and Irigoien 2008). Like the traditional light microscopy approach, the FlowCam relies primarily on cell features for phytoplankton identification, and thus is best suited to large, morphologically distinct phytoplankton groups (Lombard et al. 2019;Kenitz et al. 2023). ...

Convening Expert Taxonomists to Build Image Libraries for Training Automated Classifiers

... The limited overlap between the two approaches could also be due to temporal variations due to the sampling strategy adopted (up to ca. one week between different samplings), despite discrepancies remain also when samples for eDNA analysis and morphological identification contextually collected (as in the Trieste port) were compared. At the same time, although bloom-forming species might have considerable quantitative changes even within 7 days, changes in the census of species present are unlikely to be significant in 7 days (Kenitz et al., 2023;Suthers et al., 2009;Zingone et al., 2023). ...

Environmental and ecological drivers of harmful algal blooms revealed by automated underwater microscopy

... Functional traits-based approaches thus offer new opportunities to unravel the relation between the diversity of zooplankton traits, their trade-offs and marine ecosystem functioning (Martini et al., 2021;Barton et al., 2013;Kiørboe et al., 2018a, b). More recently, a variety of modelling frameworks were developed 70 to enable more elaborate representations of zooplankton functional diversity (Negrete-García et al., 2022;Serra-Pompei et al., 2020;Chenillat et al., 2021). In particular, recent studies on the feeding strategies of mesozooplankton have demonstrated the complexity of such a representation, where similar traits are represented through a large range of parameters based on different hypotheses (Visser, 2007;Serra-Pompei et al., 2020). ...

Plankton energy flows using a global size-structured and trait-based model
  • Citing Article
  • September 2022

Progress In Oceanography