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Abstract The flux of carbon through the labile dissolved organic matter (DOM) pool supports marine microbial communities and represents the fate of approximately half of marine net primary production (NPP). However, the behavior of individual chemical structures that make up labile DOM remain largely unknown. We performed 12 uptake kinetics and two uptake competition experiments on the abundant betaine osmolytes glycine betaine (GBT) and homarine. Combining uptake kinetics with dissolved metabolite measurements, we quantified fluxes through the DOM pool. Fluxes were correlated with particulate concentrations and ranged from 0.53 to 41 and 0.003 to 0.54 nmol L−1 d−1for GBT and homarine, respectively, equivalent to up to 1.2% of NPP. Turnover times of dissolved GBT and homarine ranged from 1 to 57 d. Betaines and sulfoniums such as dimethylsulfoniopropionate competitively inhibited homarine uptake. Our results quantify GBT and homarine cycling and suggest an important role for uptake competition in regulating dissolved metabolite concentrations and fluxes.
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Dissolved Organic Matter in the Global Ocean: A Primer
Marine dissolved organic matter (DOM) holds ~660 billion metric tons of carbon, making it one of Earth’s major carbon reservoirs that is exchangeable with the atmosphere on annual to millennial time scales. The global ocean scale dynamics of the pool have become better illuminated over the past few decades, and those are very briefly described here. What is still far from understood is the dynamical control on this pool at the molecular level; in the case of this Special Issue, the role of microgels is poorly known. This manuscript provides the global context of a large pool of marine DOM upon which those missing insights can be built.
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- Award ID(s):
- 2023500
- PAR ID:
- 10293016
- Date Published:
- Journal Name:
- Gels
- Volume:
- 7
- Issue:
- 3
- ISSN:
- 2310-2861
- Page Range / eLocation ID:
- 128
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Surface ocean marine dissolved organic matter (DOM) serves as an important reservoir of carbon (C), nitrogen (N), and phosphorus (P) in the global ocean, and is produced and consumed by both autotrophic and heterotrophic communities. While prior work has described distributions of dissolved organic carbon (DOC) and nitrogen (DON) concentrations, our understanding of DOC:DON:DOP stoichiometry in the global surface ocean has been limited by the availability of DOP concentration measurements. Here, we estimate mean surface ocean bulk and semi‐labile DOC:DON:DOP stoichiometry in biogeochemically and geographically defined regions using newly available marine DOM concentration databases. Global mean surface ocean bulk (C:N:P = 387:26:1) and semi‐labile (C:N:P = 179:20:1) DOM stoichiometries are higher than Redfield stoichiometry, with semi‐labile DOM stoichiometry similar to that of global mean surface ocean particulate organic matter (C:N:P = 160:21:1) reported in a recent compilation. DOM stoichiometry varies across ocean basins, ranging from 251:17:1 to 638:43:1 for bulk and 83:15:1 to 414:49:1 for semi‐labile DOM C:N:P, respectively. Surface ocean DOP concentration exhibits larger relative changes than DOC and DON, driving surface ocean gradients in DOC:DON:DOP stoichiometry. Inferred autotrophic consumption of DOP helps explain intra‐ and inter‐basin patterns of marine DOM C:N:P stoichiometry, with regional patterns of water column denitrification and iron supply influencing the biogeochemical conditions favoring DOP use as an organic nutrient. Specifically, surface ocean marine DOM exhibits increasingly P‐depleted stoichiometries from east to west in the Pacific and from south to north in the Atlantic, consistent with patterns of increasing P stress and alleviated iron stress.more » « less
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Francois Morel (Ed.)Marine dissolved organic matter (DOM) is a major reservoir that links global carbon, nitrogen, and phosphorus. DOM is also important for marine sulfur biogeochemistry as the largest water column reservoir of organic sulfur. Dissolved organic sulfur (DOS) can originate from phytoplankton-derived biomolecules in the surface ocean or from abiotically “sulfurized” organic matter diffusing from sulfidic sediments. These sources differ in 34S/32S isotope ratios (δ34S values), with phytoplankton-produced DOS tracking marine sulfate (21‰) and sulfurized DOS mirroring sedimentary porewater sulfide (∼0 to –10‰). We measured the δ34S values of solid-phase extracted (SPE) DOM from marine water columns and porewater from sulfidic sediments. Marine DOM_SPE δ34S values ranged from 14.9‰ to 19.9‰ and C:S ratios from 153 to 303, with lower δ34S values corresponding to higher C:S ratios. Marine DOM_SPE samples showed consistent trends with depth: δ34S values decreased, C:S ratios increased, and δ13C values were constant. Porewater DOM_SPE was 34S-depleted (∼-0.6‰) and sulfur-rich (C:S ∼37) compared with water column samples. We interpret these trends as reflecting at most 20% (and on average ∼8%) contribution of abiotic sulfurized sources to marine DOS_SPE and conclude that sulfurized porewater is not a main component of oceanic DOS and DOM. We hypothesize that heterogeneity in δ34S values and C:S ratios reflects the combination of sulfurized porewater inputs and preferential microbial scavenging of sulfur relative to carbon without isotope fractionation. Our findings strengthen links between oceanic sulfur and carbon cycling, supporting a realization that organic sulfur, not just sulfate, is important to marine biogeochemistry.more » « less
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null (Ed.)The oceans teem with heterotrophic bacterioplankton that play an appreciable role in the uptake of dissolved organic carbon (DOC) derived from phytoplankton net primary production (NPP). As such, bacterioplankton carbon demand (BCD), or gross heterotrophic production, represents a major carbon pathway that influences the seasonal accumulation of DOC in the surface ocean and, subsequently, the potential vertical or horizontal export of seasonally accumulated DOC. Here, we examine the contributions of bacterioplankton and DOM to ecological and biogeochemical carbon flow pathways, including those of the microbial loop and the biological carbon pump, in the Western North Atlantic Ocean (∼39–54°N along ∼40°W) over a composite annual phytoplankton bloom cycle. Combining field observations with data collected from corresponding DOC remineralization experiments, we estimate the efficiency at which bacterioplankton utilize DOC, demonstrate seasonality in the fraction of NPP that supports BCD, and provide evidence for shifts in the bioavailability and persistence of the seasonally accumulated DOC. Our results indicate that while the portion of DOC flux through bacterioplankton relative to NPP increased as seasons transitioned from high to low productivity, there was a fraction of the DOM production that accumulated and persisted. This persistent DOM is potentially an important pool of organic carbon available for export to the deep ocean via convective mixing, thus representing an important export term of the biological carbon pump.more » « less
- Free Publicly Accessible Full Text
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Accepted Manuscript
- Journal Article:
- https://doi.org/10.3390/gels7030128
