Particulate Organic Carbon Degradation Research Articles

Reactive transport modeling of organic carbon degradation in marine methane hydrate systems

Natural methane hydrate has often been observed in sand layers that contain no particulate organic carbon (POC), but are surrounded by organic-rich, fine-grained marine muds. In this paper, we develop a reactive transport model (RTM) of a microbially-mediated set of POC degradation reactions, including hydrolysis of POC driven by extracellular enzymes, fermentation of the resulting high-molecular weight dissolved organic carbon (HMW-DOC), and methanogenesis that consumes low-molecular weight dissolved organic carbon (LMW-DOC). These processes are mediated by two groups of microbes, fermenters and methanogens that are heterogeneously distributed in different lithologies, with the largest numbers of microbes in the large pores of coarse-grained layers. We find that the RTM can reproduce methane hydrate occurrences observed in two different geological environments, at Walker Ridge Site 313-H (Gulf of Mexico) and IODP Site U1325 (Cascadia Margin). We also find that microbes can degrade POC even if they are physically separated, as extracellular enzymes and DOC can diffuse away from where they are produced by microbes. Microbial activity is highest at relatively early times after burial at shallow depths and near lithological boundaries, where concentration gradients transport solutes to intervals that contain the most microbes.

Export of particulate organic carbon (POC) in the eddy region of the tropical northwest Pacific

We examined particulate organic carbon (POC) export using 238U–234Th disequilibrium in the tropical northwest Pacific Ocean, where numerous eddies are present. We obtained data from an anticyclonic eddy in 2019 and from both anticyclonic and cyclonic eddies in 2020. In 2019, excess 234Th and higher POC concentrations were observed in the upper 100 m layer inside the anticyclonic eddy compared with the outer area of the eddy (the reference site). We speculate that the peculiar feature of excess 234Th in the surface layer was caused by horizontal transport of POC into the eddy and consequent POC degradation and release of particulate 234Th to a dissolved form. However, in 2020, lower POC concentrations with 234Th deficiency were observed in both cyclonic and anticyclonic eddies relative to the reference site. In both years, POC export was lower in the cores of the anticyclonic and cyclonic eddies relative to the reference site. We propose that severe nutrient depletion in the upper 150 m layer hindered nutrient supply by vertical water movement in the eddies. Despite the low POC export at 100 m depth, POC export at 500 m depth was comparable to values observed at 500 m depth at Station Papa in the more productive northeastern Pacific region. Our results imply that POC export into the deep ocean interior in this region may not be as low as expected from the low primary productivity in the euphotic zone.

Microbes contribute to setting the ocean carbon flux by altering the fate of sinking particulates

Sinking particulate organic carbon out of the surface ocean sequesters carbon on decadal to millennial timescales. Predicting the particulate carbon flux is therefore critical for understanding both global carbon cycling and the future climate. Microbes play a crucial role in particulate organic carbon degradation, but the impact of depth-dependent microbial dynamics on ocean-scale particulate carbon fluxes is poorly understood. Here we scale-up essential features of particle-associated microbial dynamics to understand the large-scale vertical carbon flux in the ocean. Our model provides mechanistic insight into the microbial contribution to the particulate organic carbon flux profile. We show that the enhanced transfer of carbon to depth can result from populations struggling to establish colonies on sinking particles due to diffusive nutrient loss, cell detachment, and mortality. These dynamics are controlled by the interaction between multiple biotic and abiotic factors. Accurately capturing particle-microbe interactions is essential for predicting variability in large-scale carbon cycling.

Seasonal variability in particulate organic carbon degradation in the Kolyma River, Siberia

Major Arctic rivers are undergoing changes due to climate warming with higher discharge and increased amounts of solutes and organic carbon (OC) draining into rivers and coastal seas. Permafrost thaw mobilizes previously frozen OC to the fluvial network where it can be degraded into greenhouse gases and emitted to the atmosphere. Degradation of OC during downstream transport, especially of the particulate OC (POC), is however poorly characterized. Here, we quantified POC degradation in the Kolyma River, the largest river system underlain with continuous permafrost, during 9–15 d whole-water incubations (containing POC and dissolved OC—DOC) during two seasons: spring freshet (early June) and late summer (end of July). Furthermore, we examined interactions between dissolved and particulate phases using parallel incubations of filtered water (only DOC). We measured OC concentrations and carbon isotopes (δ13C, Δ14C) to define carbon losses and to characterize OC composition, respectively. We found that both POC composition and biodegradability differs greatly between seasons. During summer, POC was predominantly autochthonous (47%–95%) and degraded rapidly (∼33% loss) whereas freshet POC was largely of allochthonous origin (77%–96%) and less degradable. Gains in POC concentrations (up to 31%) were observed in freshet waters that could be attributed to flocculation and adsorption of DOC to particles. The demonstrated DOC flocculation and adsorption to POC indicates that the fate and dynamics of the substantially-sized DOC pool may shift from degradation to settling, depending on season and POC concentrations—the latter potentially acting to attenuate greenhouse gas emissions from fluvial systems. We finally note that DOC incubations without POC present may yield degradation estimates that do not reflect degradation in the in situ river conditions, and that interaction between dissolved and particulate phases may be important to consider when determining fluvial carbon dynamics and feedbacks under a changing climate.

Respiration by "marine snow" at high hydrostatic pressure: Insights from continuous oxygen measurements in a rotating pressure tank.

It is generally anticipated that particulate organic carbon (POC) for most part is degraded by attached microorganisms during the descent of “marine snow” aggregates toward the deep sea. There is, however, increasing evidence that fresh aggregates can reach great depth and sustain relatively high biological activity in the deep sea. Using a novel high‐pressure setup, we tested the hypothesis that increasing levels of hydrostatic pressure inhibit POC degradation in aggregates rapidly sinking to the ocean interior. Respiration activity, a proxy for POC degradation, was measured directly and continuously at up to 100 MPa (corresponding to 10 km water depth) in a rotating pressure tank that keeps the aggregates in a sinking mode. Model diatom‐bacteria aggregates, cultures of the aggregate‐forming diatom Skeletonema marinoi, and seawater microbial communities devoid of diatoms showed incomplete and complete inhibition of respiration activity when exposed to pressure levels of 10–50 and 60–100 MPa, respectively. This implies reduced POC degradation and hence enhanced POC export to hadal trenches through fast‐sinking, pressure‐exposed aggregates. Notably, continuous respiration measurements at ≥50 MPa revealed curved instead of linear oxygen time series whenever S. marinoi was present, which was not captured by discrete respiration measurements. These curvatures correspond to alternating phases of high and low respiration activity likely connected to pressure effects on unidentified metabolic processes in S. marinoi.

DNA stable-isotope probing reveals potential key players for microbial decomposition and degradation of diatom-derived marine particulate matter.

Microbially mediated decomposition of particulate organic carbon (POC) is a central component of the oceanic carbon cycle, controlling the flux of organic carbon from the surface ocean to the deep ocean. Yet, the specific microbial taxa responsible for POC decomposition and degradation in the deep ocean are still unknown. To target the active microbial lineages involved in these processes, 13C‐labeled particulate organic matter (POM) was used as a substrate to incubate particle‐attached (PAM) and free‐living microbial (FLM) assemblages from the epi‐ and bathypelagic zones of the New Britain Trench (NBT). By combining DNA stable‐isotope probing and Illumina Miseq high‐throughput sequencing of bacterial 16S rRNA gene, we identified 14 active bacterial taxonomic groups that implicated in the decomposition of 13C‐labeled POM at low and high pressures under the temperature of 15°C. Our results show that both PAM and FLM were able to decompose POC and assimilate the released DOC. However, similar bacterial taxa in both the PAM and FLM assemblages were involved in POC decomposition and DOC degradation, suggesting the decoupling between microbial lifestyles and ecological functions. Microbial decomposition of POC and degradation of DOC were accomplished primarily by particle‐attached bacteria at atmospheric pressure and by free‐living bacteria at high pressures. Overall, the POC degradation rates were higher at atmospheric pressure (0.1 MPa) than at high pressures (20 and 40 MPa) under 15°C. Our results provide direct evidence linking the specific particle‐attached and free‐living bacterial lineages to decomposition and degradation of diatomic detritus at low and high pressures and identified the potential mediators of POC fluxes in the epi‐ and bathypelagic zones.

Reconstructing organic matter sources and rain rates in the southern West Pacific Warm Pool during the transition from the deglaciation period to early Holocene

Transient features in the organic carbon content of deep-sea sediment cores resulting from changes in the flux and/or quality of sedimentary organic matter are not uncommon. We examined the geochemical characteristics of sediments retrieved with a gravity corer from the northwestern Solomon Sea (3908 m water depth), southern West Pacific Warm Pool (WPWP). δ13C and δ15N of sedimentary organic matter, together with TOC/TN data suggest that the organic material is characterized by a mixture of marine and terrestrial origins with a higher contribution from marine algae. The data were analyzed with an inverse non-steady-state reaction-transport model to examine the variability and magnitude of particulate organic carbon (POC) flux to the seafloor during the transition between the deglaciation period and early Holocene. Measured POC content and porewater NO3−, NH4+, DIC and SO42− concentrations were used to constrain the model. Hindcast results revealed that POC flux decreased from 75 to 37.5 μg cm−2 yr−1 during the deglaciation–early Holocene transition. The rate of POC degradation in the present setting is slightly lower compared to that in the pre-Holocene setting. The synchronous decline in the relative contribution of terrestrial organic matter input and rapid sea level rise during this transition suggest that sea level, rather than surface productivity, is the dominant factor controlling the POC deposition flux in the Solomon Sea. This is conceivable because the sampling site is proximal to high-relief islands with high rainfall, a well-developed submarine canyon system and narrow and steep continental margins. Consequently, we suggest that deep-water basins in proximity to similar high-relief mountainous islands in the tropical Pacific may represent important sinks for terrestrial organic material, especially during sea level lowstands.

Organic Carbon Processing During Transport Through Boreal Inland Waters: Particles as Important Sites

AbstractThe degradation and transformation of organic carbon (C) in inland waters result in significant CO2 emissions from inland waters. Even though most of the C in inland waters occurs as dissolved organic carbon (DOC), studies on particulate organic carbon (POC) and how it influences the overall reactivity of organic C in transport are still scarce. We sampled 30 aquatic ecosystems following an aquatic continuum including peat surface waters, streams, rivers, and lakes. We report DOC and POC degradation rates, relate degradation patterns to environmental data across these systems, and present qualitative changes in dissolved organic matter and particulate organic matter during degradation. Microbial degradation rates of POC were approximately 15 times higher compared to degradation of DOC, with POC half‐lives of only 17 ± 3 (mean ± SE) days across all sampled aquatic ecosystems. Rapid POC decay was accompanied by a shift in particulate C:N ratios, whereas dissolved organic matter composition did not change at the time scale of incubations. The faster degradation of the POC implies a constant replenishment to sustain natural POC concentrations. We suggest that degradation of organic matter transported through the inland water continuum might occur to a large extent via transition of DOC into more rapidly cycling POC in nature, for example, triggered by light. In this way, particles would be a dominant pool of organic C processing across the boreal aquatic continuum, partially sustained by replenishment via flocculation of DOC.

A new look at the multi-G model for organic carbon degradation in surface marine sediments for coupled benthic–pelagic simulations of the global ocean

Abstract. The kinetics of particulate organic carbon (POC) mineralization in marine surface sediments is not well constrained. This creates considerable uncertainties when benthic processes are considered in global biogeochemical or Earth system circulation models to simulate climate–ocean interactions and biogeochemical tracer distributions in the ocean. In an attempt to improve our understanding of the rate and depth distribution of organic carbon mineralization in bioturbated (0–20 cm) sediments at the global scale, we parameterized a 1-D diagenetic model that simulates the mineralization of three discrete POC pools (a multi-G model). The rate constants of the three reactive classes (highly reactive, reactive, refractory) are fixed and determined to be 70, 0.5 and ∼ 0.001 yr−1, respectively, based on the Martin curve model for pelagic POC degradation. In contrast to previous approaches, however, the reactivity of the organic material degraded in the seafloor is continuous with, and set by, the apparent reactivity of material sinking through the water column. Despite the simplifications of describing POC remineralization using G-type approaches, the model is able to simulate a global database (185 stations) of benthic oxygen and nitrate fluxes across the sediment–water interface in addition to porewater oxygen and nitrate distributions and organic carbon burial efficiencies. It is further consistent with degradation experiments using fresh phytoplankton reported in a previous study. We propose that an important yet mostly overlooked consideration in upscaling approaches is the proportion of the reactive POC classes reaching the seafloor in addition to their reactivity. The approach presented is applicable to both steady-state and non-steady state scenarios, and links POC degradation kinetics in sedimentary environments to water depth and the POC rain rate to the seafloor.

Bacterioplankton drawdown of coral mass-spawned organic matter

Coral reef ecosystems are highly sensitive to microbial activities that result from dissolved organic matter (DOM) enrichment of their surrounding seawater. However, the response to particulate organic matter (POM) enrichment is less studied. In a microcosm experiment, we tested the response of bacterioplankton to a pulse of POM from the mass-spawning of Orbicella franksi coral off the Caribbean coast of Panama. Particulate organic carbon (POC), a proxy measurement for POM, increased by 40-fold in seawater samples collected during spawning; 68% degraded within 66 h. The elevation of multiple hydrolases presumably solubilized the spawn-derived POM into DOM. A carbon budget constructed for the 275 µM of degraded POC showed negligible change to the concentration of dissolved organic carbon (DOC), indicating that the DOM was readily utilized. Fourier transform ion cyclotron resonance mass spectrometry shows that the DOM pool became enriched with heteroatom-containing molecules, a trend that suggests microbial alteration of organic matter. Our sensitivity analysis demonstrates that bacterial carbon demand could have accounted for a large proportion of the POC degradation. Further, using bromodeoxyuridine immunocapture in combination with 454 pyrosequencing of the 16S ribosomal RNA gene, we surmise that actively growing bacterial groups were the primary degraders. We conclude that coral gametes are highly labile to bacteria and that such large capacity for bacterial degradation and alteration of organic matter has implications for coral reef health and coastal marine biogeochemistry.

Fate of leaf litter deposits and impacts on oxygen availability in bank filtration column studies

Degradation of particulate organic carbon (POC) such as leaf litter might deplete dissolved oxygen within the upper layers of bank filtration, an efficient and robust barrier for pathogens and for various organic micro-pollutants (OMP) in water supply systems worldwide. The degradation of OMP during bank filtration depends on the redox conditions. The present study aimed at identifying the impacts and fates of different local leaves on the oxygen consumption and the possible biological degradation of indicator OMP. Oxygen concentrations initially decreased within the columns from around 8 mg/L in the influent to low concentrations indicating extensive consumption within a short travel distance. Still a substantial oxygen consumption was observed after 250 days. OMP concentrations were not significantly affected by the microbial processes. A layer of calcium carbonate crystallites was observed on the POC layer. Some leaf fragments appeared to be persistant towards degradation and the carbon content relative to nitrogen and sulfur contents decreased within 250 days. The results demonstrate that trees at bank filtration sites might have a strong long-term impact on the subsurface redox conditions.

Interactions between iron and organic carbon in a sandy beach subterranean estuary

Understanding the behavior of terrestrially derived dissolved organic carbon (DOC) through subterranean estuaries (STEs) is essential for determining the carbon budget in coastal waters. However, few studies exist on the interaction of organic carbon (OC) and iron (Fe) in these dynamic systems, where fresh groundwater mixes with recirculated seawater. Here, we focused on the origin and behavior of DOC, and we quantified the relative proportion of OC trapped by reactive Fe-hydroxides along a sandy beach STE. The δ13C-DOC signal in beach groundwater seems to respond rapidly to OC inputs. Our results show a terrestrial imprint from the aquifer matrix dominated by the degradation of particulate organic carbon (POC) issue from an old soil horizon composed of terrestrial plant detritus (14C dating ~800 to 700 years B.P) which is buried below the Holocene sand. Even though the system can be sporadically affected by massive inputs of marine OC, this transient marine imprint seems to be rapidly evacuated from the STE. As reported in soil and in marine mud, Fe–OC trapping occurs in the sandy sediment of the STE. At the groundwater–seawater interface, newly precipitated reactive Fe-hydroxides interact with and trap terrestrial OC independently of the DOC origin in beach groundwater. The molecular fractionation of DOC along the STE and preferential trapping of terrestrial compounds favor the in situ degradation and/or export of non-Fe-stabilized marine-derived molecules to coastal waters. These findings support the idea that the sandy beach STE acts as a transient sink for terrestrial OC at the land–sea interface and contributes to the regulation of marine vs. terrestrial carbon exports to coastal waters.

On the effect of low oxygen concentrations on bacterial degradation of sinking particles

In marine oxygen (O2) minimum zones (OMZs), the transfer of particulate organic carbon (POC) to depth via the biological carbon pump might be enhanced as a result of slower remineralisation under lower dissolved O2 concentrations (DO). In parallel, nitrogen (N) loss to the atmosphere through microbial processes, such as denitrification and anammox, is directly linked to particulate nitrogen (PN) export. However it is unclear (1) whether DO is the only factor that potentially enhances POC transfer in OMZs, and (2) if particle fluxes are sufficient to support observed N loss rates. We performed a degradation experiment on sinking particles collected from the Baltic Sea, where anoxic zones are observed. Sinking material was harvested using surface-tethered sediment traps and subsequently incubated in darkness at different DO levels, including severe suboxia (<0.5 mg l−1 DO). Our results show that DO plays a role in regulating POC and PN degradation rates. POC(PN) degradation was reduced by approximately 100% from the high to low DO to the lowest DO. The amount of NH4+ produced from the pool of remineralising organic N matched estimations of NH4+ anammox requirements during our experiment. This anammox was likely fueled by DON degradation rather than PON degradation.

Quorum Sensing Plays a Complex Role in Regulating the Enzyme Hydrolysis Activity of Microbes Associated with Sinking Particles in the Ocean

The concentration of atmospheric carbon dioxide is directly linked to the sinking of photosynthetically derived particulate organic carbon (POC) from surface waters to deep waters. This process, known as the marine biological carbon pump, removes carbon from exchange with the atmosphere, thus regulating global climate. Recent evidence suggests that microbial chemical communication systems (e.g. quorum sensing) amongst heterotrophic bacteria associated with sinking POC, significantly influences their hydrolytic enzyme activity and, as such, may affect the efficiency of the biological carbon pump. Here, we present data showing that a class of quorum sensing molecules, acylated homeserine lactones (AHLs) substantially impact hydrolytic phosphatase, aminopeptidase, and lipase activity in samples of sinking particles collected from the Atlantic and Pacific Ocean. Incubations of sinking particles amended with exogenous AHLs showed both stimulated and inhibited rates of activity after 24 hours of incubation, suggesting a critical link between bacterial AHL signaling mechanisms and the rate of POC degradation. Further experiments reveal that hydrolytic pathways could be affected within a few hours of amendment with AHLs, suggesting that microbial communities are able to dynamically modify their metabolic pathways in response to perceived quorum sensing. Finally, the concentration of the AHL amendment also affected hydrolytic activity. Our results indicated that quorum sensing has the potential to influence hydrolytic activity in a range of oceanic environments, but response also vary significantly as a function of the type of AHL, their concentration, and response time. AHL-based quorum sensing may be thought of as a global language among marine bacteria, but it is highly complex.

3-D numerical modelling of methane hydrate accumulations using PetroMod

Within the German gas hydrate initiative SUGAR, a new 2-D/3-D module simulating the biogenic generation of methane from organic matter and the formation of gas hydrates has been developed and included in the petroleum systems modelling software package PetroMod®. Typically, PetroMod® simulates the thermogenic generation of multiple hydrocarbon components (oil and gas), their migration through geological strata, finally predicting oil and gas accumulations in suitable reservoir formations. We have extended PetroMod® to simulate gas hydrate accumulations in marine and permafrost environments by the implementation of algorithms describing (1) the physical, thermodynamic, and kinetic properties of gas hydrates; and (2) a kinetic continuum model for the microbially mediated, low temperature degradation of particulate organic carbon in sediments. Additionally, the temporal and spatial resolutions of PetroMod® were increased in order to simulate processes on time scales of hundreds of years and within decimetres of spatial extension. In order to validate the abilities of the new hydrate module, we present here results of a theoretical layer-cake model. The simulation runs predict the spatial distribution and evolution in time of the gas hydrate stability field, the generation and migration of thermogenic and biogenic methane gas, and its accumulation as gas hydrates.

The challenges of quantifying the carbon stored in Arctic marine gas hydrate

The quantification of the carbon stored in gas hydrate (GH) bearing marine sediments still remains a challenge. Despite recent efforts to develop approaches to better estimate the GH inventory globally, these estimates are still highly unconstrained due to insufficient field data and poor understanding of the mechanisms fuelling the GH stability zone (GHSZ). Here we use geophysically-derived GH saturations to constraint estimates of model-derived Arctic marine GH inventory at present. We also estimate the potential carbon released from GH dissociation under a seabed warming of 2 °C over 100 yr. We estimate an inventory ranging between 0.28 and 541 Gt of carbon, which upper bound results in average GH saturations of 0.25%. Our upper bound is mainly controlled by our imposed upwards carbon-rich fluid flow of 0.01 cm yr−1 and it is five times greater than the most recent estimate that only considers in-situ degradation of particulate organic carbon (POC). To obtain the seismically-inferred GH saturations of 5–10% offshore west of Svalbard and in the Beaufort Sea, an upwards advection of carbon-rich fluids equivalent to 0.02–0.04 cm yr−1 is required. This mechanism may be the most important source of carbon reaching the GHSZ in Arctic marine sediments. A 2 °C seabed temperature increase over 100 yr may reduce the GH inventory by about 88.44% (0.7 Gt C) if POC is the only source, and by about 5.4% (29.7 Gt C) if the main source of carbon is the upwards advection of carbon-rich fluids.

The effect of temperature on organic carbon degradation in marine sediments.

The degradation of sedimentary particulate organic carbon (POC) is a key carbon cycle process that fuels the deep subseafloor biosphere. The reactivity of POC is expected to decrease with increasing sediment age, severely restricting the energy available to microorganisms. Conversely, increasing temperatures during burial have been proposed to stimulate POC degradation, possibly supplying significant energy to the deep biosphere. To test the importance of temperature, we assembled POC measurements in two global sets of drill sites where sediments underwent either relatively low or high temperatures during burial, which should have resulted in different rates of POC degradation. For ages 5–10 Ma, the decrease of the average POC content with burial is clearly more pronounced in the sites with high temperature histories. Our results support the hypothesis that temperature is one of the fundamental controls on the rate of POC degradation within deeply buried marine sediments.

Effectiveness of preservatives and poisons on sediment trap material in freshwater environments

To estimate the effectiveness of preservative/poisons on sediment trap material in freshwater environments, we measured the ratio of particulate organic matter retention [particulate organic carbon (POC) and nitrogen (PON), particulate phosphorus (PP)] using simulated sediment trap material (SSTM). SSTM was collected in summer and fall from depths of 30 and 85 m in the mesotrophic northern basin of Lake Biwa, Japan. All SSTM was incubated in buffered formalin, sodium azide (NaN3) and mercuric chloride (HgCl2) solutions for a period of 56 days. The retention ratio of POC, PON and PP of SSTM was measured throughout the course of the experiments. Results showed that buffered formalin and HgCl2 were very effective in preserving POC. Although NaN3 was less effective at preventing degradation of POC, the degradation process as a function of time was described with the double-exponential decay equation extremely well. Buffered formalin and HgCl2 were also effective in preserving PON, but less effective than for POC. To ensure accurate measurements of PON vertical flux, therefore, one should estimate the decomposition kinetics of PON in sediment trap material. None of the preservatives used in this study was effective for preserving PP, which was rapidly degraded within a week. However, the degradation process was also fully described by the equation, and this will make it possible to accurately estimate PP vertical flux.

Biogeochemical drivers of the fate of riverine mercury discharged to the global and Arctic oceans

AbstractRivers discharge 28 ± 13 Mmol yr−1 of mercury (Hg) to ocean margins, an amount comparable to atmospheric deposition to the global oceans. Most of the Hg discharged by rivers is sequestered by burial of benthic sediment in estuaries or the coastal zone, but some is evaded to the atmosphere and some is exported to the open ocean. We investigate the fate of riverine Hg by developing a new global 3‐D simulation for Hg in the Massachusetts Institute of Technology ocean general circulation model. The model includes plankton dynamics and carbon respiration (DARWIN project model) coupled to inorganic Hg chemistry. Results are consistent with observed spatial patterns and magnitudes of surface ocean Hg concentrations. We use observational constraints on seawater Hg concentrations and evasion to infer that most Hg from rivers is sorbed to refractory organic carbon and preferentially buried. Only 6% of Hg discharged by rivers (1.8 Mmol yr−1) is transported to the open ocean on a global basis. This fraction varies from a low of 2.6% in East Asia due to the barrier imposed by the Korean Peninsula and Japanese archipelago, up to 25% in eastern North America facilitated by the Gulf Stream. In the Arctic Ocean, low tributary particle loads and efficient degradation of particulate organic carbon by deltaic microbial communities favor a more labile riverine Hg pool. Evasion of Hg to the Arctic atmosphere is indirectly enhanced by heat transport during spring freshet that accelerates sea ice melt and ice rafting. Discharges of 0.23 Mmol Hg yr−1 from Arctic rivers can explain the observed summer maximum in the Arctic atmosphere, and this magnitude of releases is consistent with recent observations. Our work indicates that rivers are major contributors to Hg loads in the Arctic Ocean.

Toward a parameterization of global‐scale organic carbon mineralization kinetics in surface marine sediments

AbstractAn empirical function is derived for predicting the rate‐depth profile of particulate organic carbon (POC) degradation in surface marine sediments including the bioturbated layer. The rate takes the form of a power law analogous to the Middelburg function. The functional parameters were optimized by simulating measured benthic O2 and NO3− fluxes at 185 stations worldwide using a diagenetic model. The novelty of this work rests with the finding that the vertically resolved POC degradation rate in the bioturbated zone can be determined using a simple function where the POC rain rate is the governing variable. Although imperfect, the model is able to fit 71% of paired O2 and NO3− fluxes to within 50% of measured values. It further provides realistic geochemical concentration‐depth profiles, NO3− penetration depths, and apparent first‐order POC mineralization rate constants. The model performs less well on the continental shelf due to the high sediment heterogeneity there. When applied to globally resolved maps of rain rate, the model predicts a global denitrification rate of 182 ± 88 Tg yr−1 of N and a POC burial rate of 107 ± 52 Tg yr−1 of C with a mean carbon burial efficiency of 6.1%. These results are in very good agreement with published values. Our proposed function is conceptually simple, requires less parameterization than multi‐G‐type models, and is suitable for nonsteady state applications. It provides a basis for more accurately simulating benthic nutrient fluxes and carbonate dissolution rates in Earth system models.