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Whereas recruitment success for many fisheries depends on coincident timing of larvae with abundance peaks of their prey, less can be more in the tropical/subtropical spawning areas of bluefin tunas if lower but steady food resources are offset by reduced larval vulnerability to pelagic predators. To understand larval habitat characteristics for Southern Bluefin Tuna (SBT), we quantified microbial community carbon flows based on growth and grazing rates from depth profiles of dilution incubations and carbon biomass assessments from microscopy and flow cytometry (FCM) during their peak spawning off NW Australia (Indian Ocean) in February 2022. Two Chla-based estimates of phytoplankton production gave differing offsets due to cycling or mixotrophy, exceeding 14C net community production on average (677 ± 98 versus 447 ± 43 mg C m−2 d−1). Productivity was higher than in the Gulf of Mexico spawning area for Atlantic Bluefin Tuna but less than similar studies of oceanic upwelling regions. Microzooplankton grazing averaged 482 ± 63 mg C m−2 d−1 (71 ± 13 % of production). Two measurement variables for Prochlorococcus gave average production and grazing rates of 282 ± 36 and 248 ± 32 mg C m−2 d−1 (86 ± 6 % grazed). Prochlorococcus comprised almost half of production and grazing fluxes in the upper (0–25 m) euphotic zone where SBT larvae reside. Prochlorococcus declined and eukaryotic phytoplankton and heterotrophic bacteria increased in relative importance in the lower euphotic zone. These results describe relatively classic open-ocean oligotrophic conditions as the food web base for nutritional flows to SBT larvae. 

ABSTRACT Phytoplankton community composition during austral summer 2022 in the Argo Abyssal Plain (Argo Basin), a 5000-m deep area northwest of the Australian continent in the eastern Indian Ocean, is described in detail, including phytoplankton abundance, biomass, size structure, taxonomic identifications through DNA and pigment analyses, as well as the percent of functional mixotrophs. The region was characterized by warm (up to 30.5°C), stratified, oligotrophic (nitrogen-limited) waters, with integrated euphotic zone (EZ) chlorophyll a (CHLa) of 13 mg m^-2. The EZ mean CHLawas low in the upper layer (0.085 µg L^-1) and 0.32 µg L^-1at the pronounced deep CHLamaxima. EZ-integrated phytoplankton carbon averaged 1229 mg C m^-2.Prochlorococcuswas the dominant taxon throughout the EZ, but the lower EZ had ∼4-times more eukaryotic carbon biomass than the upper EZ, along with a distinct community. In the upper EZ, prymnesiophytes, dinoflagellates and prasinophyte taxa without prasinoxanthin had the highest contributions to monovinyl chlorophyll a (MV-CHLa). In the lower EZ the community was more diverse, with prymnesiophytes, dinoflagellates, prasinophyte taxa with prasinoxanthin, pelagophytes, and cryptophytes all comprising significant contributions to MV-CHLa. Diatoms were a minor part of the community. In the upper EZ, a higher percent of the community showed mixotrophy (35-84%) relative to the lower EZ (30-51%). Although a low abundance, nitrogen-fixing organisms (symbionts of diatoms and cyanobacteria taxa) were ubiquitous. Overall, the community was similar to that found at the Hawaii Ocean Time-series site and the central Gulf of Mexico. 

Abstract Photosynthesis in the surface ocean and subsequent export of a fraction of this fixed carbon leads to carbon dioxide sequestration in the deep ocean. Ecological relationships among plankton functional groups and theoretical relationships between particle size and sinking rate suggest that carbon export from the euphotic zone is more efficient when communities are dominated by large organisms. However, this hypothesis has never been tested against measured size spectra spanning the >5 orders of magnitude found in plankton communities. Using data from five ocean regions (California Current Ecosystem, North Pacific subtropical gyre, Costa Rica Dome, Gulf of Mexico, and Southern Ocean subtropical front), we quantified carbon‐based plankton size spectra from heterotrophic bacteria to metazoan zooplankton (size class cutoffs varied slightly between regions) and their relationship to net primary production and sinking particle flux. Slopes of the normalized biomass size spectra (NBSS) varied from −1.6 to −1.2 (median slope of −1.4 equates to large 1–10 mm organisms having a biomass equal to only 7.6% of the biomass in small 1–10 μm organisms). Net primary production was positively correlated with the NBSS slope, with a particularly strong relationship in the microbial portion of the size spectra. While organic carbon export co‐varied with NBSS slope, we found only weak evidence that export efficiency is related to plankton community size spectra. Multi‐variate statistical analysis suggested that properties of the NBSS added no explanatory power over chlorophyll, primary production, and temperature. Rather, the results suggest that both plankton size spectra and carbon export increase with increasing system productivity. 

Picophytoplankton populations [Prochlorococcus,Synechococcus(SYN), and picoeukaryotes] are dominant primary producers in the open ocean and projected to become more important with climate change. Their fates can vary, however, with microbial food web complexities. In the California Current Ecosystem, picophytoplankton biomass and abundance peak in waters of intermediate productivity and decrease at higher production. Using experimental data from eight cruises crossing the pronounced CCE trophic gradient, we tested the hypothesis that these declines are driven by intensified grazing on heterotrophic bacteria (HBAC) passed to similarly sized picophytoplankton via shared predators. Results confirm previously observed distributions as well as significant increases in bacterial abundance, cell growth, and grazing mortality with primary production. Mortalities of picophytoplankton, however, diverge from the bacterial mortality trend such that relative grazing rates on SYN compared to HBAC decline by 12-fold between low and high productivity waters. The large shifts in mortality rate ratios for coexisting populations are not explained by size variability but rather suggest high selectivity of grazer assemblages or tightly coupled tradeoffs in microbial growth advantages and grazing vulnerabilities. These findings challenge the long-held view that protistan grazing mainly determines overall biomass of microbial communities while viruses uniquely regulate diversity by “killing the winners”. 

Abstract The Southern Ocean contributes substantially to the global biological carbon pump (BCP). Salps in the Southern Ocean, in particular Salpa thompsoni , are important grazers that produce large, fast-sinking fecal pellets. Here, we quantify the salp bloom impacts on microbial dynamics and the BCP, by contrasting locations differing in salp bloom presence/absence. Salp blooms coincide with phytoplankton dominated by diatoms or prymnesiophytes, depending on water mass characteristics. Their grazing is comparable to microzooplankton during their early bloom, resulting in a decrease of ~1/3 of primary production, and negative phytoplankton rates of change are associated with all salp locations. Particle export in salp waters is always higher, ranging 2- to 8- fold (average 5-fold), compared to non-salp locations, exporting up to 46% of primary production out of the euphotic zone. BCP efficiency increases from 5 to 28% in salp areas, which is among the highest recorded in the global ocean. 

Abstract A flow cytometry method for enumerating marine heterotrophic bacteria and phytoplankton in a living or preserved sample using a low power solid state near‐ultraviolet laser is described. The method uses Hoechst 34580 to stain DNA in microbial cells in seawater samples. This stain is optimally excited at 375 nm unlike the similar Hoechst 33342, which requires ~ 350 nm excitation only available on more expensive lasers. Phytoplankton abundances from the Hoechst 34580 method are comparable to those of unstained samples and when analyzed by the Hoechst 33342 staining method. With this new method, nonpigmented marine bacteria and phytoplankton abundances are obtained simultaneously in a single sample as the Hoechst emission wavelength (~ 450 nm) is well separated from the emission wavelengths of chlorophyll and phycoerythrin fluorescence. Bacteria abundances are similar between this new method and those obtained with established Hoechst 33342 and SybrGreen I methods. Precision estimates (coefficient of variation) on populations with abundances near ~ 10⁵cells mL⁻¹are 1–3%, increasing to 3–9% at lower cell concentrations of 10³cells mL⁻¹. The Hoechst 34580 method is simple, requiring no heating or pretreatment with RNAse, can be used on unpreserved and formaldehyde‐preserved cells, and is amenable to at‐sea use with portable, compact, low power‐requiring flow cytometers.