Sediment CH4 Research Articles

Cyanobacteria decay alters CH4 and CO2 produced hotspots along vertical sediment profiles in eutrophic lakes

Cyanobacteria-derived organic carbon has been reported to intensify greenhouse gas emissions from lacustrine sediments. However, the specific processes of CH4 and CO2 production and release from sediments into the atmosphere remain unclear, especially in eutrophic lakes. To investigate the influence of severe cyanobacteria accumulation on the production and migration of sedimentary CH4 and CO2, this study examined the different trophic level lakes along the middle and lower reaches of the Yangtze River. The results demonstrated that eutrophication amplified CH4 and CO2 emissions, notably in Lake Taihu, where fluxes peaked at 929.9 and 7222.5 μmol/m2·h, mirroring dissolved gas levels in overlying waters. Increased sedimentary organic carbon raised dissolved CH4 and CO2 concentrations in pore-water, with isotopic tracking showing cyanobacteria-derived carbon specifically elevated CH4 and CO2 in surface sediment pore-water more than in deeper layers. Cyanobacteria-derived carbon deposition on surface sediment boosted organic carbon and moisture levels, fostering an anaerobic microenvironment conducive to enhanced biogenic CH4 and CO2 production in surface sediments. In the microcosm systems with the most severe cyanobacteria accumulation, average CH4 and CO2 concentrations in surface sediments reached 6.9 and 2.3 mol/L, respectively, surpassing the 4.7 and 1.4 mol/L observed in bottom sediments, indicating upward migration of CH4 and CO2 hotspots from deeper to surface layers. These findings enhance our understanding of the mechanisms underlying lake sediment carbon emissions induced by eutrophication and provide a more accurate assessment of lake carbon emissions.

Efficient oxidation attenuates porewater‐derived methane fluxes in mangrove waters

AbstractMangroves store significant amounts of carbon in both sediment and water. Methane (CH4) is often produced in anoxic, organic‐rich sediments during carbon degradation and released to overlying waters via porewater exchange. Yet, a portion of CH4 can be oxidized to CO2 before emission. Here, we investigate whether CH4 oxidation impacts its emissions using high‐temporal resolution CH4 concentration and stable isotope (δ13C‐CH4) observations collected over 14 tidal cycles in 2 Brazilian mangrove creeks with no river inputs. We found higher CH4 concentrations (~ 150 nM) more depleted in 13C (−75‰) during low tide than high tide at both creeks. Similar δ13C‐CH4 values between low tide surface waters and porewaters further suggest tidally driven porewater exchange as the main source of CH4. More 13C‐enriched CH4 in surface waters and surface sediments than deep sediments indicate partial CH4 oxidation prior to exchange with the atmosphere. A stable isotope mass balance revealed that 17–58% of CH4 was oxidized at rates of 3–25 μmol m−2 d−1 in the water column of tidal creeks. A larger portion of deep porewater CH4 (45–61%) was oxidized in sediments prior to porewater exchange with surface creek waters. The two mangrove creeks had average water–air CH4 fluxes of 51–109 μmol m−2 d−1 over spring‐neap tidal cycles. These aquatic CH4 emissions offset only < 3% of the mangroves' soil carbon sequestration. Overall, CH4 oxidation in both surface water and sediment attenuated CH4 emissions to the atmosphere.

Predicting Methane Formation Rates of Freshwater Sediments in Different Biogeographic Regions

AbstractFreshwater lakes and reservoirs cover a small fraction of the Earth, however their emission of the greenhouse gas methane (CH4) from the sediment to the atmosphere is disproportionately high. Currently, there is still a limited understanding of the links between sediment characteristics and CH4 formation. Earlier studies have indicated that sediment age and nitrogen content are related to sediment CH4 formation rates, but it is uncertain such relationships are valid across gradients of sediment characteristics. We therefore measured potential CH4 formation rates in multiple layers of sediment sampled from nine lakes situated in the temperate, boreal and alpine biogeographic regions of Sweden, thus differing in productivity, catchment and climate properties. Potential CH4 formation varied over 3 orders of magnitude, and was broadly related to the quantity and reactivity of organic matter, and generally decreased with sediment depth. Sediment age and total nitrogen content were found to be the key controlling factors of potential CH4 formation rates, together explaining 62% of its variability. Moreover, the model developed from the Swedish lake sediment data was able to successfully predict the potential CH4 formation rates in reservoirs situated in different biogeographic regions of Brazil (R2 = 0.62). Therefore, potential CH4 formation rates in sediments of highly contrasting lakes and reservoirs, from Amazonia to alpine tundra, could be accurately predicted using one common model (RMSE = 1.6 in ln‐units). Our model provides a valuable tool to improve estimates of CH4 emission from lakes and reservoirs, and illustrates the fundamental regulation of microbial CH4 formation by organic matter characteristics.

Impact of Reservoir Operation Policies on Spatiotemporal Dynamics of Sediment Methane Production and Release in a Large Reservoir

AbstractReservoir operation policies affect sediment methane (CH4) production and pathways through complex influence on hydrodynamic and biogeochemical processes in reservoir water and sediment. However, the underlying influencing mechanisms, especially the impact of operations on sediment CH4 production and pathways, remain poorly understood. This study combines a physical‐biogeochemical model with a reservoir operation model to evaluate operation impacts on spatiotemporal sediment CH4 production and release dynamics and to analyze affiliated processes and driving factors. Three typical operation policies (i.e., standard, hedging, eco‐friendly) are selected to create the operation scenarios, and a coupled physical‐biogeochemical model is adopted to simulate and compare sediment CH4 production, consumption, diffusion, and ebullition under these scenarios. The methods are applied in the second largest reservoir in China (i.e., Danjiangkou Reservoir) as a case study. Results show that annual total sediment CH4 production among the scenarios ranges from 285.9 to 298.3 Gg C year−1, while operation scenario outcomes significantly differ. Specifically, a significant CH4 percentage (34%–39%) is oxidized in surface sediment while the remaining escapes sediment through diffusion and ebullition. Although diffusion accounts for >60% of the annual sediment CH4 release, sediment ebullition ultimately dominates atmospheric CH4 emissions. Annual total atmospheric CH4 emissions range from 42.8 to 71.1 Gg C year−1 and account for 14%–25% of the annual total sediment production among the three scenarios. The differences demonstrate that reservoir operations significantly impact CH4 pathways and atmospheric emissions. This study provides implications for reservoir managers to coordinate socioeconomic and ecological protection while mitigating CH4 emission targets.

Widespread dominance of methane ebullition over diffusion in freshwater aquaculture ponds

An ever-increasing demand for protein-rich food sources combined with dwindling wild fish stocks has caused the aquaculture sector to boom in the last two decades. Although fishponds are potentially strong emitters of the greenhouse gas methane (CH4), little is known about the magnitude, pathways, and drivers of these emissions. We measured diffusive CH4 emissions at the margin and in the center of 52 freshwater fishponds in Brazil. In a subset of ponds (n = 31) we additionally quantified ebullitive CH4 fluxes and sampled water and sediment for biogeochemical analyses. Sediments (n = 20) were incubated to quantify potential CH4 production. Ebullitive CH4 emissions ranged between 0 and 477 mg m−2 d−1 and contributed substantially (median 85%) to total CH4 emissions, surpassing diffusive emissions in 81% of ponds. Diffusive CH4 emissions were higher in the center (median 11.4 mg CH4 m−2 d−1) than at the margin (median 6.1 mg CH4 m−2 d−1) in 90% of ponds. Sediment CH4 production ranged between 0 and 3.17 mg CH4 g C−1 d−1. We found no relation between sediment CH4 production and in situ emissions. Our findings suggest that dominance of CH4 ebullition over diffusion is widespread across aquaculture ponds. Management practices to minimize the carbon footprint of aquaculture production should focus on reducing sediment accumulation and CH4 ebullition.

Competitive methane bubble growth in aquatic muds

Methane (CH4) bubbles residing in shallow aquatic muds pose a significant threat to the environment. Impeded by the muddy sediment opacity and insufficient resolution for their characterization, past studies overlooked bubble interactions as they grow. Here, the competitive fracture-driven growth of CH4 bubble pair with different initial sizes in the aquatic muds is simulated, using a mechanical/reaction-transport numerical model. Mechanical and solute transport interactions were found to dominate at the different stages of the bubble growth, both retarding the smaller competitive bubble growth. The stress from large competitive bubble affects the inner pressure and diffusive CH4 flux to the smaller bubble, causing its slower initial growth (at t < 40 s). The large competitive bubble also diverts CH4 from the smaller one later on, thus inhibiting its growth even more. Bubble stress interactions may produce more laterally oriented smaller bubble and significant deformations of the larger one, both amplified under the decreasing distance between the growing bubble pair. Competitive bubble growth may shape a bubble size distribution pattern observed in the lab experiments and in situ, which may promote muddy sediment CH4 gas retention and produce gas domes. The latter acts as pockmark precursors whose formation induces a violent gas release to the water column and potentially to the atmosphere. Our study presents a basis for a proper upscaling to various effective gassy muddy sediment characteristics and gas retention evolution transient models, while preserving the single bubble growth descriptors. It contributes to evaluation and even reduction of a long-persisting uncertainty related to CH4 flux from the shallow aquatic sediments.

Methanogens limited to lower rhizosphere and to an atypical salt marsh niche along a pristine intertidal mangrove continuum

AbstractMangroves are valuable ecosystems that facilitate primary production, carbon sequestration, and regulation of greenhouse gas (GHG) cycles in coastal sediments, with microorganisms playing key roles. Specialized bacteria and archaea compete for energy and resources in mangrove sediments to inhabit optimal ecological niches and can produce or consume methane (CH4)—a potent GHG—in the process. CH4 cycling in mangroves has gained growing attention, yet uncertainties regarding functional and spatial distributions of microorganisms remain. Here, we demonstrate that in a pristine mangrove forest, CH4 concentrations and methanogen communities are concentrated within lower or below rhizosphere depths. We also reveal atypical niches for methanogens in the upper tidal salt marsh zone where vegetation is sparse and highest methanogens abundances were detected at deepest depths (4715 reads g−1) despite relatively high redox potentials (&gt; 250 mV). Pore water CH4 concentrations were highest at the deepest depth within the mangrove forest (max. 3.40 ± 0.21 μM) and coincided with the highest sediment CH4 fluxes (276.4 ± 54.2 μmol m−2d−1) and methanotroph abundances at the surface (1309 reads g−1). Sediment CH4 oxidation fractions between the deepest (60 cm) and shallowest (5 cm) depths were estimated between 18.8% and 64.9%. Positive correlation between crab burrows and CH4 fluxes suggests that CH4 from deeper sediment and salt marsh niches can be transported via conduits to the atmosphere. The spatial data from this study highlights the importance of investigating CH4 dynamics across estuarine ecosystem gradients to better understand the complex roles of vital coastal vegetation zones in the face of a changing climate.

Evaluating the Feedback of the Reservoir Methane Cycle to Climate Warming under Hydrological Uncertainty

Freshwater reservoirs are widely recognized as methane (CH4) emission hotspots. Existing research has shown that temperature and hydrological conditions significantly affect wetland CH4 cycling processes. However, the feedback of the CH4 cycle to climate warming remains unclear for deep reservoirs where seasonal water thermal stratification exists. This study combined a reservoir CH4 cycling model and a Statistical DownScaling Model (SDSM) to evaluate reservoir CH4 cycling feedbacks under multiple climate change scenarios while accounting for hydrological uncertainty. Daily air temperatures in 2100 were predicted by the combination of the CanESM5 model and a SDSM. To address hydrological uncertainty, we selected three representative hydrological years (i.e., wet, normal, and dry) to create hydrological scenarios. Results showed that annual sediment CH4 production increased with warming, ranging 323.1–413.7 × 103 t C year−1 among multiple scenarios. Meanwhile, the CH4 oxidation percentage decreased with warming, which meant warming promoted sediment CH4 release non-linearly; 67.8–84.6% of sediment ebullient flux was ultimately emitted to the atmosphere (51.3–137.7 × 103 t C year−1), which showed ebullition was the dominant emission pathway. Higher air temperatures and drier conditions generally promote reservoir emissions. This study is helpful for predicting reservoir emissions while directing decision-making for reservoir sustainability.

Coastal acidification alters estuarine sediment nitrous oxide and methane fluxes

AbstractThe impact of coastal acidification on sediment nitrous oxide (N2O) and methane (CH4) fluxes is largely unknown. We exposed temperate estuarine sediments to moderate (pH 7.3) and extreme (pH 6.3) acidification. Sediments were collected from two sites—one exposed to high and the other to low nitrogen loading. We demonstrate that low pH has a strong effect on greenhouse gas fluxes. The response, in terms of both magnitude and direction, was site specific. Sediments from the high nitrogen loading site exhibited increased N2O fluxes and decreased CH4 fluxes under moderate and extreme acidification. In contrast, sediments from the low nitrogen loading site exhibited decreased N2O fluxes under moderate and extreme acidification while CH4 fluxes both decreased (moderate) and increased (extreme). This study highlights the dynamic response of sediment N2O and CH4 fluxes to low pH and emphasizes the need for deeper understanding of ofcoastal acidification impacts on sediment biogeochemistry.

The greenhouse effect of antibiotics: The influence pathways of antibiotics on methane release from freshwater sediment

The impact of antibiotics on methane (CH4) release from sediment involves both CH4 production and consumption processes. However, most relevant studies lack a discussion of the pathways by which antibiotics affect CH4 release and do not highlight the role played by the sediment chemical environment in this influence mechanism. Here, we collected field surface sediments and grouped them with various antibiotic combination concentration gradients (50, 100, 500, 1000 ng g−1) under a 35-day indoor anaerobic constant temperature incubation. We found that the positive effect of antibiotics on sediment CH4 release potential appeared later than the positive effect on sediment CH4 release flux. Still, the positive effect of high-concentration antibiotics (500, 1000 ng g−1) occurred with a lag in both processes. Also, the positive effect of high-concentration antibiotics was significantly higher than low-concentration antibiotics (50, 100 ng g−1) in the later incubation period (p < 0.05). We performed a multi-collinearity assessment of sediment biochemical indicators, followed by a generalized linear model with negative binomial regression (GLM-NB) to obtain essential variables. In particular, we conducted the interaction analysis on CH4 release potential and flux regression for the influence pathways construction. The partial least-squares path modeling (PLS-PM) demonstrated that the positive effect of antibiotics on CH4 release (Total effect = 0.2579) was primarily attributed to their effect on the sediment chemical environment (Direct effect = 0.5107). These findings greatly expand our understanding of the antibiotic greenhouse effect in freshwater sediment. Further studies should more carefully consider the effects of antibiotics on the sediment chemical environment, and continuously improve the mechanistic studies of antibiotics on sediment CH4 release.

A rationale for higher ratios of CH4 to CO2 production in warmer anoxic freshwater sediments and soils

A rationale for higher ratios of <scp>CH₄</scp> to <scp>CO₂</scp> production in warmer anoxic freshwater sediments and soils

Microbial methane cycling in sediments of Arctic thermokarst lagoons.

Thermokarst lagoons represent the transition state from a freshwater lacustrine to a marine environment, and receive little attention regarding their role for greenhouse gas production and release in Arctic permafrost landscapes. We studied the fate of methane (CH4 ) in sediments of a thermokarst lagoon in comparison to two thermokarst lakes on the Bykovsky Peninsula in northeastern Siberia through the analysis of sediment CH4 concentrations and isotopic signature, methane-cycling microbial taxa, sediment geochemistry, lipid biomarkers, and network analysis. We assessed how differences in geochemistry between thermokarst lakes and thermokarst lagoons, caused by the infiltration of sulfate-rich marine water, altered the microbial methane-cycling community. Anaerobic sulfate-reducing ANME-2a/2b methanotrophs dominated the sulfate-rich sediments of the lagoon despite its known seasonal alternation between brackish and freshwater inflow and low sulfate concentrations compared to the usual marine ANME habitat. Non-competitive methylotrophic methanogens dominated the methanogenic community of the lakes and the lagoon, independent of differences in porewater chemistry and depth. This potentially contributed to the high CH4 concentrations observed in all sulfate-poor sediments. CH4 concentrations in the freshwater-influenced sediments averaged 1.34 ± 0.98 μmol g-1 , with highly depleted δ13 C-CH4 values ranging from -89‰ to -70‰. In contrast, the sulfate-affected upper 300 cm of the lagoon exhibited low average CH4 concentrations of 0.011 ± 0.005 μmol g-1 with comparatively enriched δ13 C-CH4 values of -54‰ to -37‰ pointing to substantial methane oxidation. Our study shows that lagoon formation specifically supports methane oxidizers and methane oxidation through changes in pore water chemistry, especially sulfate, while methanogens are similar to lake conditions.

Important Role of Biogas and Secretions in the Formation of Biological Fluid Sediment under Cyanobacterial Bloom Biomass Degradation

In eutrophic shallow lakes, cyanobacterial blooms will occur frequently and then accumulate on sediments, leading to the formation of biological fluid sediment. In this study, the formation process of biological fluid sediment was investigated in microcosm experiments by monitoring the variations in gas, sediment physicochemical properties, and microorganisms during 30 days. It was found that variations in sediment height reached the maximum value on day 8 (0.53 cm) with the minimum sediment density (1.04 g cm–3). Meanwhile, the amount of carbon dioxide (CO2) produced through fermentation was larger than methane (CH4) during the initial 4 days. Then, the amount of CH4 drastically increased, resulting in the release of gas from sediments. In addition, a high amount of extracellular polymer substances (EPSs) was produced and led to sediment particle agglomeration, which benefited in maintaining the structure of biological fluid sediment. Through the microbial community analysis, it was found that the strong symbiotic structure of the microbial community in the early stage provided favorable conditions for the formation of CH4 in sediments. The results of this study can clarify the formation mechanism of biological fluid sediment and provide help for understanding the effect of biogas and secretions on the sediment properties in shallow lakes.

Vertical Hydrologic Exchange Flows Control Methane Emissions from Riverbed Sediments.

CH4 emissions from inland waters are highly uncertain in the current global CH4 budget, especially for streams, rivers, and other lotic systems. Previous studies have attributed the strong spatiotemporal heterogeneity of riverine CH4 to environmental factors such as sediment type, water level, temperature, or particulate organic carbon abundance through correlation analysis. However, a mechanistic understanding of the basis for such heterogeneity is lacking. Here, we combine sediment CH4 data from the Hanford reach of the Columbia River with a biogeochemical-transport model to show that vertical hydrologic exchange flows (VHEFs), driven by the difference between river stage and groundwater level, determine CH4 flux at the sediment-water interface. CH4 fluxes show a nonlinear relationship with the magnitude of VHEFs, where high VHEFs introduce O2 into riverbed sediments, which inhibit CH4 production and induce CH4 oxidation, and low VHEFs cause transient reduction in CH4 flux (relative to production) due to reduced advective CH4 transport. In addition, VHEFs lead to the hysteresis of temperature rise and CH4 emissions because high river discharge caused by snowmelt in spring leads to strong downwelling flow that offsets increasing CH4 production with temperature rise. Our findings reveal how the interplay between in-stream hydrologic flux besides fluvial-wetland connectivity and microbial metabolic pathways that compete with methanogenic pathways can produce complex patterns in CH4 production and emission in riverbed alluvial sediments.

Peculiarities of CH4 and CO2 Distribution in Sediments of the Arctic Seas

The distribution of the concentrations of CH4 and CO2 and other gases in the sediments of the Kara, Laptev and East Siberian seas was studied. A correlation was found between CH4 and CO2 in most sediment cores. The correlation coefficient R for the sediments of the Kara Sea ranges from 0.58 to 0.97 and does not depend on the gas distribution with depth. Methanogenesis in marine sediments is presumably associated with sulfate reduction, and hydrogenotrophic methanogenesis leads to an increase in CH4 concentration against the background of high CO2 concentration. The high concentration of dimethyl sulfide in the sediments indicates the simultaneous formation of CH4 and CO2 through methylotrophic methanogenesis with the participation of CH3SCH3. In the upper layers of the sediment, opposite trends in the CH4 and CO2 distribution can be observed. The fact that the correlation coefficients between CH4 and CO2 gases in the sediments of the Laptev Sea acquire both negative and positive values is probably related to the fact that gas formation processes in the upper layers of the sediment captured by short columns differ from those of deep layers.

Peculiarities of CH4 and CO2 Distribution in Sediments of the Arctic Seas

Peculiarities of CH4 and CO2 Distribution in Sediments of the Arctic Seas

The crucial role of deep-sourced methane in maintaining the subseafloor sulfate budget

Methane (CH4) is a powerful greenhouse gas and its largest reservoir on Earth is held in marine sediments. CH4 in marine sediments is mainly stored in gas-hydrate reservoirs and deep sedimentary strata along continental margins, where large amounts of deep-sourced CH4 ascend to different degrees toward the seafloor. However, the amount of deep-sourced CH4 and its role in subseafloor carbon and sulfur cycling remains poorly constrained. We analyzed sulfate (SO42−) profiles of 157 sites along with previous published 85 sites to determine the regional distribution and amount of SO42− reduction for an area of 1.23 × 105 km2 of the northern South China Sea. Then we compared these obtained results with estimates based on sedimentation rates from the same area. Significantly higher regional SO42− flux estimates based on SO42− profiles (4.26 × 10−3 Tmol a−1), compared to lower estimates based on sedimentation rates (1.23 × 10−3 Tmol a−1), reflect abundant ascending deep-sourced CH4. The difference of the regional SO42− flux estimates (3.03 × 10−3 Tmol a−1) represents the amount of SO42− reduced by CH4 through the anaerobic oxidation of CH4 (AOM). Deep-sourced CH4 contributes 71% to total SO42− consumption in the study area, largely exceeding SO42− consumption by organoclastic sulfate reduction. Our findings substantiate that deep-sourced CH4 governs subseafloor carbon and sulfur cycling to a previously underrated extent, fueling extensive chemosynthesis-based ecosystems along continental slope and rise.

Biotic and abiotic controls on sediment carbon dioxide and methane fluxes under short-term experimental warming

Due to the differences in biotic and abiotic factors between soil and sediments, the predicted linkages between biotic and abiotic factors and soil carbon dioxide (CO2) and methane (CH4) fluxes under warming may not be suitable for sediments. Additionally, the combination of biotic and abiotic factors which determines sediment temperature-dependent CO2 and CH4 fluxes remains unresolved. To address this issue, different types of sediments (including lake, small river and pond sediments) collected from 30 sites across the Yangtze River Basin were incubated under short-term experimental warming. During the incubating phase, the sediment temperature-dependent CO2 and CH4 fluxes as well as the accompanying biotic factors (organic carbon and microbial community) and abiotic factors (pH and dissolved oxygen (DO)) were determined and analyzed synthetically. Our results indicated that sediment CO2 fluxes were more sensitive than CH4 fluxes to warming, which might lead to a relatively large CO2 contribution to total greenhouse gas emissions in a warming climate. Additionally, temperature-dependent CO2 fluxes in pond sediments were more sensitive than those in lake sediments. Random forest analysis indicated that DO greatly affected the variation in the sediment temperature-dependent CO2 fluxes, whereas Methanococcales primarily predicted the CH4 fluxes under warming. DO also highly affected the variation in the temperature sensitivity of CH4 fluxes, whereas pH mostly predicted the temperature sensitivity of CO2 fluxes. Our findings suggest that biotic and abiotic factors, especially DO, pH and the composition of methanogens, coregulate CO2 and CH4 emissions in response to climate warming. Therefore, biotic and abiotic factors should be considered in the models for predication and investigation of sediment organic carbon dynamics under climate change.

МЕТАН И СЕРОВОДОРОД В ДОННЫХ ОТЛОЖЕНИЯХ ВОДОХРАНИЛИЩ И ПРУДОВ БАССЕЙНА АЗОВСКОГО МОРЯ

Gas-geochemical studies of bottom sediments and water of Sokolovsky, Grushevsky, Artemovsky, Veselovsky, Proletarsky, Tsimlyansky reservoirs and other dammed reservoirs were carried out. Concentrations of CH4 and ΣH2S in sediments vary from 0.02 to 61.3 μg/g and from &amp;lt;0.01 to 8.36 mg/g of wet sediment, respectively. The highest concentrations of CH4 are observed in the deposits of the Artemovsky, Tsimlyansky and Veselovsky reservoirs, and ΣH2S – in the deposits of the Proletarian, Tsimlyansky and Grushevsky reservoirs. The distribution of CH4 and ΣH2S along the vertical profile of sediments is characterized, as a rule, by an increase in concentrations from the surface layer to the subsurface horizons, in which their maximum peak is recorded, after which the concentrations decrease. The difference between the distribution of ΣH2S and the distribution of CH4 is the more frequent fixation of maximum concentrations of ΣH2S in less deep layers of sediments. The percentage of CH4 from the sum of the studied reduced gases (the coefficient of methanization of КCH4) in sediments varies from 0.004 to 11.1 %, which indicates a significant dominance of the process of sulfate reduction over the process of methanogenesis. The closeness of the relationships of the concentrations of CH4 and ΣH2S between themselves and the values of КCH4, pH and Eh deposits is analyzed.

The effects of climate warming on microbe-mediated mechanisms of sediment carbon emission

Due to significant differences in biotic and abiotic properties of soils compared to those of sediments, the predicted underlying microbe-mediated mechanisms of soil carbon emissions in response to warming may not be applicable for estimating similar emissions from inland water sediments. We addressed this issue by incubating different types of sediments, (including lake, small river, and pond sediments) collected from 36 sites across the Yangtze River basin, under short-term experimental warming to explore the effects of climate warming on sediment carbon emission and the underlying microbe-mediated mechanisms. Our results indicated that under climate warming CO2 emissions were affected more than CH4 emissions, and that pond sediments may yield a greater relative contribution of CO2 to total carbon emissions than lake and river sediments. Warming-induced CO2 and CH4 increases involve different microbe-mediated mechanisms; Warming-induced sediment CO2 emissions were predicted to be directly positively driven by microbial community network modularity, which was significantly negatively affected by the quality and quantity of organic carbon and warming-induced variations in dissolved oxygen, Conversely, warming-induced sediment CH4 emissions were predicted to be directly positively driven by microbial community network complexity, which was significantly negatively affected by warming-induced variations in pH. Our findings suggest that biotic and abiotic drivers for sediment CO2 and CH4 emissions in response to climate warming should be considered separately when predicting sediment organic carbon decomposition dynamics resulting from climate change.