We found that in the phosphate (PO4)‐depleted western subtropical North Atlantic Ocean, small‐sized pigmented eukaryotes (P‐Euk; < 5
- Award ID(s):
- 1458070
- PAR ID:
- 10459610
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Limnology and Oceanography
- Volume:
- 64
- Issue:
- 6
- ISSN:
- 0024-3590
- Page Range / eLocation ID:
- p. 2424-2440
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
null (Ed.)Daily oscillations in photosynthetically active radiation strongly influence the timing of metabolic processes in picocyanobacteria, but it is less clear how the light-dark cycle affects the activities of their consumers. We investigated the relationship between marine picocyanobacteria and nanoplanktonic consumers throughout the diel cycle to determine whether heterotrophic and mixotrophic protists (algae with phagotrophic ability) display significant periodicity in grazing pressure. Carbon biomass of Prochlorococcus and Synechococcus was estimated continuously from abundances and cell size measurements made by flow cytometry. Picocyanobacterial dynamics were then compared to nanoplankton abundances and ingestion of fluorescently labeled bacteria measured every 4 h during a 4 d survey in the North Pacific Subtropical Gyre. Grazing of the labeled bacteria by heterotrophic nanoplankton was significantly greater at night than during the day. The grazing activity of mixotrophic nanoplankton showed no diel periodicity, suggesting that they may feed continuously, albeit at lower rates than heterotrophic nanoplankton, to alleviate nutrient limitation in this oligotrophic environment. Diel changes in Prochlorococcus biomass indicated that they could support substantial growth of nanoplankton if those grazers are the main source of picocyanobacterial mortality, and that grazers may contribute to temporally stable abundances of picocyanobacteria.more » « less
-
Abstract The13C/12C of dissolved inorganic carbon (
δ 13CDIC) carries valuable information on ocean biological C‐cycling, air‐sea CO2exchange, and circulation. Paleo‐reconstructions of oceanic13C from sediment cores provide key insights into past as changes in these three drivers. As a step toward full inclusion of13C in the next generation of Earth system models, we implemented13C‐cycling in a 1° lateral resolution ocean‐ice‐biogeochemistry Geophysical Fluid Dynamics Laboratory (GFDL) model driven by Common Ocean Reference Experiment perpetual year forcing. The model improved the mean of modernδ 13CDICover coarser resolution GFDL‐model implementations, capturing the Southern Ocean decline in surfaceδ 13CDICthat propagates to the deep sea via deep water formation. Controls onδ 13CDICof the deep‐sea are quantified using both observations and model output. The biological control is estimated from the relationship between deep‐sea Pacificδ 13CDICand phosphate (PO4). Theδ 13CDIC:PO4slope from observations is revised to a value of 1.01 ± 0.02‰ (μ mol kg−1)−1, consistent with a carbon to phosphate ratio of organic matter (C:Porg) of 124 ± 10. Model output yields a lowerδ 13CDIC:PO4than observed due to too low C:Porg. The ocean circulation impacts deep modernδ 13CDICin two ways, via the relative proportion of Southern Ocean and North Atlantic deep water masses, and via the preindustrialδ 13CDICof these water mass endmembers. Theδ 13CDICof the endmembers ventilating the deep sea are shown to be highly sensitive to the wind speed dependence of air‐sea CO2gas exchange. Reducing the coefficient for air‐sea gas exchange following OMIP‐CMIP6 protocols improves significantly surfaceδ 13CDICrelative to previous gas exchange parameterizations. -
Abstract The
J = 5.5 → 4.5 andJ = 5 → 4 transitions of PO and PN, respectively, have been imaged in the envelope of hypergiant star VY Canis Majoris (VY CMa) using the Atacama Large Millimeter/submillimeter Array with angular resolutions of 0.″2 and 1.″5 and data from the Submillimeter Telescope of the Arizona Radio Observatory. These maps are the first high-fidelity images of PO and PN in a circumstellar envelope. Both molecules are primarily present in a spherical, star-centered region with a radius ∼60R *(0.″5), indicating formation by LTE chemistry and then condensation into grains. PN, however, shows additional, fan-shaped emission 2″ southwest of the star, coincident with dust features resolved by Hubble Space Telescope (HST), as well as four newly identified distinct structures 1″–2″ toward the north, east, and west (Cloudlets I–IV), not visible in HST images. The “SW Fan” and the cloudlets are also prominent in theJ = 5.5 → 4.5 transition of NS. The correlation of PN with NS, SiO, and dust knots in the SW Fan suggests a formation in shocked gas enhanced with nitrogen. Excess nitrogen is predicted to favor PN synthesis over PO. Abundances for PN and PO in the spherical source aref ∼ 4.4 × 10−8and 1.4 × 10−7, respectively, relative to H2. Given a cosmic abundance of phosphorus, an unusually high fraction (∼35%) is contained in PO and PN. Alternatively, the stellar winds may be enriched in P (and N) by dredge-up from the interior of VY CMa. -
Abstract We investigated competition between
Salpa thompsoni and protistan grazers during Lagrangian experiments near the Subtropical Front in the southwest Pacific sector of the Southern Ocean. Over a month, the salp community shifted from dominance by large (> 100 mm) oozooids and small (< 20 mm) blastozooids to large (~ 60 mm) blastozooids. Phytoplankton biomass was consistently dominated by nano‐ and microphytoplankton (> 2μ m cells). Using bead‐calibrated flow‐cytometry light scatter to estimate phytoplankton size, we quantified size‐specific salp and protistan zooplankton grazing pressure. Salps were able to feed at a > 10,000 : 1 predator : prey size (linear‐dimension) ratio. Small blastozooids efficiently retained cells > 1.4μ m (high end of picoplankton size, 0.6–2μ m cells) and also obtained substantial nutrition from smaller bacteria‐sized cells. Larger salps could only feed efficiently on > 5.9μ m cells and were largely incapable of feeding on picoplankton. Due to the high biomass of nano‐ and microphytoplankton, however, all salps derived most of their (phytoplankton‐based) nutrition from these larger autotrophs. Phagotrophic protists were the dominant competitors for these prey items and consumed approximately 50% of the biomass of all phytoplankton size classes each day. Using a Bayesian statistical framework, we developed an allometric‐scaling equation for salp clearance rates as a function of salp and prey size: where ESD is prey equivalent spherical diameter (µm), TL isurn:x-wiley:00243590:media:lno11770:lno11770-math-0001 S. thompsoni total length,φ = 5.6 × 10−3 ± 3.6 × 10−4,ψ = 2.1 ± 0.13,θ = 0.58 ± 0.08, andγ = 0.46 ± 0.03 and clearance rate is L d‐1salp‐1. We discuss the biogeochemical and food‐web implications of competitive interactions among salps, krill, and protozoans. -
Abstract Nutrient monitoring is important for informing management decisions to mitigate eutrophication in aquatic systems. Many nutrient monitoring programs use filter pore sizes that allow microorganisms to pass into samples and/or wait extended times between sample collection and filtration/preservation, allowing microbial processes to alter nutrient concentrations. Here, 34 sites were sampled to determine how filter pore size and filtration timing affected measured ammonium (NH4+) and orthophosphate (ortho‐P) concentrations. Three filter pore sizes (0.22, 0.45, and 0.70
μ m) were used to filter water immediately upon collection and after 5 and 22 h in a bottle. NH4+and ortho‐P concentrations varied relative to “baseline” measurements (i.e., 0.22μ m, field‐filtered samples), both over time and with different filter pore sizes, and showed no predictable direction of change based on ambient nutrient concentration or trophic status. As expected, larger relative changes occurred with lower ambient concentrations; however, for the entire dataset, samples with > 1μ mol L−1ortho‐P and > 3μ mol L−1NH4+were lower by 11 and 33%, respectively, which would result in reported nutrient concentrations that were not representative of in situ conditions. Whole‐water samples filtered after 22 h varied up to 3070% for NH4+and 480% for ortho‐P from baseline concentrations. Filtering water samples with a 0.22 filter (or 0.45μ m, at worst), immediately upon collection, should be adopted as standard practice to ensure that reported nutrient concentrations represent the most accurate measurement possible. Inconsistent and/or insufficient sampling and sample handling procedures can lead to poorly calibrated models and misinformed management and legislative decisions.