Canopy‐forming kelps are foundational species in coastal ecosystems, fixing tremendous amounts of carbon, yet we know little about the ecological and physiological determinants of dissolved organic carbon (DOC) release by kelps. We examined DOC release by the bull kelp,
Dissolved organic carbon (DOC) plays critical roles in marine carbon cycling, but its sources and sinks remain uncertain. In this study, we monitored DOC exudation rates of
- NSF-PAR ID:
- 10459806
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Global Biogeochemical Cycles
- Volume:
- 33
- Issue:
- 11
- ISSN:
- 0886-6236
- Page Range / eLocation ID:
- p. 1423-1439
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Nereocystis luetkeana , in relation to carbon fixation, nutrient uptake, tissue nitrogen content, and light availability. DOC release was approximately 3.5 times greater during the day than at night. During the day,N. luetkeana blades released an average of 16.2% of fixed carbon as DOC. Carbon fixation increased with light availability but DOC release did not, leading to a lower proportion of fixed carbon released as DOC at high light levels. We found no relationship between carbon fixation and DOC release rates measured concurrently. Rather, DOC release byN. luetkeana blades declined with marginal significance as blade tissue nitrogen content increased and with experimental nitrate addition, supporting the role of stoichiometric relationships in DOC release. Using a stable isotope (13C) tracer method, we demonstrated that inorganic carbon is rapidly fixed and released byN. luetkeana blades as13DOC, within hours. However, recently fixed carbon (13DOC) comprised less than 20% of the total DOC released, indicating that isotope studies that rely on tracer production alone may underestimate total DOC release, as it is decoupled from recent kelp productivity. Comparing carbon and nitrogen assimilation dynamics of the annual kelpN. luetkeana with the perennial kelpMacrocystis pyrifera revealed thatN. luetkeana had significantly higher carbon fixation, DOC production and nitrogen uptake rates per unit dry mass. Both kelp species were able to perform light‐independent carbon fixation at night. Carbon fixation by the annual kelpN. luetkeana is as high as 2.35 kg C·m−2·yr−1, but an average of 16% of this carbon (376 g C·m−2·yr−1) is released as DOC. As kelp forests are increasingly viewed as vehicles for carbon sequestration, it is important to consider the fate of this substantial quantity of DOC released by canopy‐forming kelps. -
Abstract Tidal channels are biogeochemical hotspots that horizontally exchange carbon (C) with marsh platforms, but the physiochemical drivers controlling these dynamics are poorly understood. We hypothesized that C‐bearing iron (Fe) oxides precipitate and immobilize dissolved organic carbon (DOC) during ebb tide as the soils oxygenate, and dissolve into the porewater during flood tide, promoting transport to the channel. The hydraulic gradient physically controls how these solutes are horizontally exchanged across the marsh platform‐tidal channel interface; we hypothesized that this gradient alters the concentration and source of C being exchanged. We further hypothesized that trace soil gases (i.e., CO2, CH4, dimethyl sulfide) are pushed out of the channel bank as the groundwater rises. To test these hypotheses, we measured porewater, surface water, and soil trace gases over two 24‐hr monitoring campaigns (i.e., summer and spring) in a mesohaline tidal marsh. We found that Fe2+and DOC were positively related during flood tide but not during ebb tide in spring when soils were more oxidized. This finding shows evidence for the formation and dissolution of C‐bearing Fe oxides across a tidal cycle. In addition, the tidal channel contained significantly (
p < 0.05) more terrestrial‐like DOC when the hydraulic gradient was driving flow toward the channel. In comparison, the channel water was saltier and contained significantly (p < 0.05) more marine‐like DOC when the hydraulic gradient reversed direction. Trace gas fluxes increased with rising groundwater levels, particularly dimethyl sulfide. These findings suggest multiple physiochemical mechanisms controlling the horizontal exchange of C at the marsh platform‐tidal channel interface. -
Abstract Investigations of abiotic and biotic contributions to dissolved organic carbon (DOC) are required to constrain microbial habitability in continental subsurface fluids. Here we investigate a large (101–283 mg C/L) DOC pool in an ancient (>1Ga), high temperature (45–55 °C), low biomass (102−104cells/mL), and deep (3.2 km) brine from an uranium-enriched South African gold mine. Excitation-emission matrices (EEMs), negative electrospray ionization (–ESI) 21 tesla Fourier-transform ion cyclotron resonance mass spectrometry (FT-ICR MS), and amino acid analyses suggest the brine DOC is primarily radiolytically oxidized kerogen-rich shales or reefs, methane and ethane, with trace amounts of C3–C6hydrocarbons and organic sulfides. δ2H and δ13C of C1–C3hydrocarbons are consistent with abiotic origins. These findings suggest water-rock processes control redox and C cycling, helping support a meagre, slow biosphere over geologic time. A radiolytic-driven, habitable brine may signal similar settings are good targets in the search for life beyond Earth.
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Abstract Rivers discharge significant quantities of dissolved organic carbon (DOC) to the ocean, yet biomarker and isotope studies suggest that terrigenous DOC makes up only a small amount DOC in the ocean. One of the removal pathways proposed for riverine DOC is sorption to marine sediments. This process is chemically selective, but whether sorption alters the isotopic composition of riverine DOC is unknown. Because there is isotopic variability across different organic compound classes, sorptive removal of DOC could also alter the isotopic composition of DOC. As a first step in addressing this question, we examined phase partitioning and isotopic composition of a riverine DOC standard in the presence of marine sediment particles. In a series of controlled experiments, the standard was mixed with marine sediment in 35‰ NaCl solution, then separated into particulate and dissolved phases for analyses of mass, δ13C, and ∆14C of organic carbon (OC). Across a range of sediment OC to DOC mass ratios (from < 0.1 to ~ 3), we found that: (1) sediment sorbed 0.8
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Abstract Drier and hotter conditions linked with anthropogenic climate change can increase wildfire frequency and severity, influencing terrestrial and aquatic carbon cycles at broad spatial and temporal scales. The impacts of wildfire are complex and dependent on several factors that may increase terrestrial deposition and the influx of dissolved organic matter (DOM) from plants into nearby aquatic systems, resulting in the darkening of water color. We tested the effects of plant biomass quantity and its interaction with fire (burned vs. unburned plant biomass) on dissolved organic carbon (DOC) concentration and degradation (biological vs. photochemical) and DOM composition in 400 L freshwater ponds using a gradient experimental design. DOC concentration increased nonlinearly with plant biomass loading in both treatments, with overall higher concentrations (>56 mg/L) in the unburned treatment shortly after plant addition. We also observed nonlinear trends in fluorescence and UV‐visible absorbance spectroscopic indices as a function of fire treatment and plant biomass, such as greater humification and specific UV absorbance at 254 nm (a proxy for aromatic DOM) over time. DOM humification occurred gradually over time with less humification in the burned treatment compared to the unburned treatment. Both burned and unburned biomass released noncolored, low molecular weight carbon compounds that were rapidly consumed by microbes. DOC decomposition exhibited a unimodal relationship with plant biomass, with microbes contributing more to DOC loss than photodegradation at intermediate biomass levels (100–300 g). Our findings demonstrate that the quantity of plant biomass leads to nonlinear responses in the dynamics and composition of DOM in experimental ponds that are altered by fire, indicating how disturbances interactively affect DOM processing and its role in aquatic environments.