Terrigenous Organic Carbon Research Articles

How human activities reshape carbon burial in estuarine sediment systems: Evidence from the Yangtze Estuary

Estuaries are critical zones for understanding the dynamics of organic carbon (OC) burial, particularly in the context of human intervention, yet detailed information remains limited. This study presents comprehensive field observations aimed at assessing the spatial and temporal variations in sedimentary OC sources, composition, and distribution within the Yangtze Estuary. By employing a three-endmember estimation, we determined the contributions of fluvial, marine, and salt marsh plants to OC in the mouth bar as 52 ± 6 %, 28 ± 12 %, and 20 ± 9 %, respectively. To address the complexities introduced by human activities and dispersal processes, we utilized a PCA-MC four-endmember model, which revealed that redispersal terrigenous organic matter from the outer estuary, categorized as “marine origin”, accounted for 26 ± 10 % re-deposited within the estuary. During the construction of the Deep Channel Navigation Project (DCNP), we observed a shift in terrigenous OC deposition from the North Passage (NP) to the South Passage (SP), along with an increased contribution from salt marsh plants. Post-DCNP completion, sedimentary OC compositions exhibited significant differences between the NP and SP, with the SP enriched in fresh terrigenous OC and the NP showing degraded signals due to dredging activities and source discrimination. Human interventions not only altered the estuarine geomorphology and hydrodynamics but also impacted OC burial and sequestration by modifying sources and compositions. This study highlights the transition of estuarine regions from carbon sinks to potential sources, underscoring the necessity for a comprehensive understanding of carbon cycle dynamics in Anthropocene-influenced estuarine environments.

High-resolution record of temporal change in organic matter burial over the past ∼8,600 years on the northwestern continental slope of the South China Sea

Sedimentary organic matter (SOM) on continental slopes in marine regions can sensitively record climatic and environmental changes. In this study, total organic carbon content (TOC), total nitrogen content (TN), and their stable isotope compositions (δ13C and δ15N) for sediments of core G02 were investigated (at ∼24.2-year resolution) to reveal the temporal variations in organic matter sources and the main controls on the sources and distribution of buried organic matter on the northwestern continental slope of the South China Sea over the last ∼8600 years. Results of a δ13C binary mixing model reveal that ∼82.3 ± 3% of SOM is derived from marine autochthonous sources. We suggest that the carbon and nitrogen contents and compositions of SOM are governed by distinct factors. The more positive δ15N values before the Pulleniatina Minimum Event occurrence are ascribed to stronger subsurface water intrusion by the Kuroshio Current, which led to enhanced subsurface denitrification and in turn counteracted the effect of mixing with surface water caused by the East Asian winter monsoon. Sedimentary δ13C values show a fluctuant decrease during ca. 8.6–3.0 cal kyr BP and a conspicuous increase during ca. 3.0–1.4 cal kyr BP. These changes are attributed to the decrease of marine productivity induced by the continuous weakening East Asian monsoon effect and the decrease of terrigenous organic carbon input induced by the weakened Indian summer monsoon precipitation, respectively. Since ca. 1.4 cal kyr BP, human activities have become the dominant factor in controlling the production and distribution of organic carbon. The results provide an important basis for understanding of source-sink processes of organic matter and the factors influencing these processes on continental slopes in low-latitude marginal seas.

Pre-aged terrigenous organic carbon biases ocean ventilation-age reconstructions in the North Atlantic

Changes in ocean ventilation have been pivotal in regulating carbon sequestration and release on centennial to millennial timescales. However, paleoceanographic reconstructions documenting changes in deep-ocean ventilation using 14C dating, may bear multidimensional explanations, obfuscating the roles of ocean ventilation played on climate evolution. Here, we show that previously inferred poorly ventilated conditions in the North Atlantic were linked to enhanced pre-aged organic carbon (OC) input during Heinrich Stadial 1 (HS1). The 14C age of sedimentary OC was approximately 13,345 ± 692 years older than the coeval foraminifera in the central North Atlantic during HS1, which is coupled to a ventilation age of 5,169 ± 660 years. Old OC was mainly of terrigenous origin and exported to the North Atlantic by ice-rafting. Remineralization of old terrigenous OC in the ocean may have contributed to, at least in part, the anomalously old ventilation ages reported for the high-latitude North Atlantic during HS1.

Determining source-specific terrigenous organic carbon contributions in sediments from the Yellow River estuary, Northeast China: A test of source apportionment models

Molecular organic geochemistry has been used effectively to determine terrigenous organic carbon (OC) contributions from different sources in modern sediments. However, mathematic modelling using source-specific parameters could be a potentially simple-effective approach to identify the terrigenous OC signals. In this study, the Yellow River estuary was chosen to probe whether source apportionment models can determine source-specific OC contributions. The end-member mixing model suggests that terrigenous OC contributed 57.0% ± 10.2% to the sedimentary OC. n-Alkane distributions were used to perform Unmix and positive matrix factorization (PMF) to separate terrigenous and autochthonous OC into more specific sources. PMF modelling delineates the contributions of high terrigenous plants, fossil OC, macrophyte-sourced OC, and bacterial and algal-sourced OC as 22.9% ± 14.3%, 26.2% ± 19.4%, 26.5% ± 19.3%, and 24.4% ± 17.1%, respectively. In assessing terrigenous contributions, PMF results (48.7% ± 13.5%) almost agrees with the end-member mixing model (57.0% ± 10.2%), consistent and comparable with previously published data (~ 50%), while Unmix (73.9% ± 18.7%) is significantly overestimated. Interestingly, macrophyte-sourced OC from coastal wetland identified by PMF was less investigated previously and should call attention in the future study. Consequently, modelling results match well with previously published data, suggesting that mathematic modelling can be an effective approach to quantitatively evaluate source-specific terrigenous OC contributions to estuary sediments and other complex aqua-land systems. However, caution must be taken in respect to the modelling uncertainty, which could be mainly induced by sample number, diversity, and robust interpretation on chemical parameters.

Terrigenous organic carbon contributes to reservoir carbon emissions: Potential role of the microbial community along a trophic gradient

Freshwaters are important carbon sources to the atmosphere and are influenced by different sources of organic carbon (OC). Microbial community is a crucial trophic network driving carbon cycling in the aquatic ecosystems. Yet, whether and how their interactions affect carbon cycling and emissions in the reservoir remains unclear. Here, we explored the interactions between phytoplankton and bacteria in reservoirs along a trophic gradient. An increase in the trophic state intensified the interaction between phytoplankton and bacteria communities. Their diversity and niche breadth indexes both decreased. Such intensification was contributed not only by the input of nutrients triggering an increase in trophic state but also by the bulk input of terrigenous OC, shaping the concentrations of CO2 and CH4 in the water phase and their air-water fluxes along the trophic gradient. Upon this, a conceptual framework was proposed to explain the positive/negative feedback of phytoplankton-bacterial interactions to carbon emissions, projecting the dual regulation of aquatic ecosystems and carbon dynamics along a trophic gradient.

Characterization of Two Marine Lignin-Degrading Consortia and the Potential Microbial Lignin Degradation Network in Nearshore Regions.

Terrestrial organic carbon such as lignin is an important component of the global marine carbon. However, the structural complexity and recalcitrant nature of lignin are deemed challenging for biodegradation. It has been speculated that bacteria play important roles in lignin degradation in the marine system. However, the extent of the involvement of marine microorganisms in lignin degradation and their contribution to the oceanic carbon cycle remains elusive. In this study, two bacterial consortia capable of degrading alkali lignin (a model compound of lignin), designated LIG-B and LIG-S, were enriched from the nearshore sediments of the East and South China Seas. Consortia LIG-B and LIG-S mainly comprised of the Proteobacteria phylum with Nitratireductor sp. (71.6%) and Halomonas sp. (91.6%), respectively. Lignin degradation was found more favorable in consortium LIG-B (max 57%) than in LIG-S (max 18%). Ligninolytic enzymes laccase (Lac), manganese peroxidase (MnP), and lignin peroxidase (LiP) capable of decomposing lignin into smaller fragments were all active in both consortia. The newly emerged low-molecular-weight aromatics, organic acids, and other lignin-derived compounds in biotreated alkali lignin also evidently showed the depolymerization of lignin by both consortia. The lignin degradation pathways reconstructed from consortium LIG-S were found to be more comprehensive compared to consortium LIG-B. It was further revealed that catabolic genes, involved in the degradation of lignin and its derivatives through multiple pathways via protocatechuate and catechol, are present not only in lignin-degrading consortia LIG-B and LIG-S but also in 783 publicly available metagenomic-assembled genomes from nine nearshore regions. IMPORTANCE Numerous terrigenous lignin-containing plant materials are constantly discharged from rivers and estuaries into the marine system. However, only low levels of terrigenous organic carbon, especially lignin, are detected in the global marine system due to the abundance of active heterotrophic microorganisms driving the carbon cycle. Simultaneously, the lack of knowledge on lignin biodegradation has hindered our understanding of the oceanic carbon cycle. Moreover, bacteria have been speculated to play important roles in the marine lignin biodegradation. Here, we enriched two bacterial consortia from nearshore sediments capable of utilizing alkali lignin for cell growth while degrading it into smaller molecules and reconstructed the lignin degradation network. In particular, this study highlights that marine microorganisms in nearshore regions mostly undergo similar pathways using protocatechuate and catechol as ring-cleavage substrates to drive lignin degradation as part of the oceanic carbon cycle, regardless of whether they are in sediments or water column.

Sources, Composition, and Export of Particulate Organic Matter Across British Estuaries

AbstractEstuaries receive and process a large amount of particulate organic carbon (POC) prior to its export into coastal waters. Studying the origin of this POC is key to understanding the fate of POC and the role of estuaries in the global carbon cycle. Here, we evaluated the concentrations of POC, as well as particulate organic nitrogen (PON), and used stable carbon and nitrogen isotopes to assess their sources across 13 contrasting British estuaries during five different sampling campaigns over 1 year. We found a high variability in POC and PON concentrations across the salinity gradient, reflecting inputs, and losses of organic material within the estuaries. Catchment land cover appeared to influence the contribution of POC to the total organic carbon flux from the estuary to coastal waters, with POC contributions >36% in estuaries draining catchments with a high percentage of urban/suburban land, and <11% in estuaries draining catchments with a high peatland cover. There was no seasonal pattern in the isotopic composition of POC and PON, suggesting similar sources for each estuary over time. Carbon isotopic ratios were depleted (−26.7 ± 0.42‰, average ± sd) at the lowest salinity waters, indicating mainly terrigenous POC (TPOC). Applying a two‐source mixing model, we observed high variability in the contribution of TPOC at the highest salinity waters between estuaries, with a median value of 57%. Our results indicate a large transport of terrigenous organic carbon into coastal waters, where it may be buried, remineralized, or transported offshore.

Monitoring and analysis of CO<sub>2</sub> and CH<sub>4</sub> fluxes in the Three Gorges Reservoir

自成库以来,三峡水库CO₂、CH₄等温室气体通量较蓄水前发生明显改变。如何科学认识和客观评估三峡水库修建及运行对其CO₂、CH₄等温室气体通量的影响备受关注。本文简要回顾了自2009年以来在三峡水库开展CO₂、CH₄等温室气体通量监测与分析工作,综述认为,现阶段三峡水库温室气体排放以水-气界面扩散释放为主要途径。陆源输入的有机碳是主导三峡水库CO₂、CH₄产生的主要碳源,但在局部区段或时段自源性有机碳的贡献亦十分显著。同蓄水前相比,三峡水库碳排放量呈现为净增加,淹没效应约占水库C净增量的20%,库区内点面源污染负荷并未对CO₂排放的净增量产生显著贡献,阻隔效应和生态系统重建效应对三峡水库碳排放的净增量产生显著贡献。近10年来,监测方法比对、监测点位优化等工作在一定程度上完善了三峡水库温室气体通量监测体系。新方法、新技术的引入也为三峡水库温室气体通量监测分析提供了有利支撑和保障,但复杂水文环境下驱动水库碳循环的水文生态机制仍不明晰,这是制约三峡水库碳通量长期趋势预测的难点。未来将通过监测技术持续创新以促进对三峡水库碳通量的精准核算,在深化基础研究的同时,仍亟待提出更科学有效的模型或方法以支撑长期趋势预测,服务水库碳管理。;Since the impoundment in 2003, the flux of CO₂, CH₄ in the Three Gorges Reservoir (TGR) has changed significantly compared with the pre-impoundment status. Accessing the influence of the construction and operation of the TGR on these greenhouse gas fluxes has attracted much attention. In this paper, we reviewed the experience of monitoring and analysis of CO₂, CH₄ fluxes in TGR since 2009. At present, air-water diffusion was the major pathway for carbon emissions in the reservoir. Terrigenous organic carbon input was the main carbon source leading the production of CO₂ and CH₄ in the reservoir. Yet, the contribution of autochthonous organic carbon seemed to be with growing significant. Compared with pre-impoundment status, a net increase of greenhouse gas emissions in TGR is evident. Flooding accounted for about 20% of the net increase of the reservoir formation. Anthropogenic pollution in the reservoir region did not significantly to the net increase of CO₂ emissions. In addition, the dam acting as barriers and reservoir aquatic ecosystem reconstruction were major contributors for the net greenhouse gas emissions. Sampling campaigns and research in the past decade promoted the improvement and optimization of monitoring system of the greenhouse gas emissions in TGR. Application of new monitoring methods and technologies also provided support and reimbursement. However, the hydro-ecological mechanism driving the carbon cycle in the reservoir under complex hydrological environment is still unclear, which is a difficulty in the long-term trend prediction of the reservoir carbon flux. In the future, innovation of monitoring technology will be applied to promote the accurate calculation of the carbon flux of TGR. It is still urgent to put forward more scientific and effective models or methods to support the long-term trend prediction and serve the reservoir carbon management.

Decadal trends in the release of terrigenous organic carbon to the Mackenzie Delta (Canadian Arctic) using satellite ocean color data (1998–2019)

Arctic rivers operate as integrators of northern high latitude regions, where large stocks of soil organic carbon (OC) are currently experiencing rapid warming. Here we show that tracking total OC in the Mackenzie Delta whose upstream catchment is underlain by permafrost soils is now possible using polar-orbiting satellite ocean color observations. A non-parametric trend analysis that is valid for hydrological data shows a significant increase in dissolved OC (DOC) as well as particulate OC (POC) concentrations in late summer (0.019 and 0.069 g m−3 year−1; p < 0.05 for both). Uncertainties of the satellite estimates of DOC and POC do not influence our results. These concentration increases are not related to changes in river discharge. Parallel increases of independent long-term (1979–2018) in situ measurements of thaw depth of the active layer, as well as meteorological and hydrological patterns suggest that these late summer increases can likely be explained by increasing inputs of permafrost OC. This study shows great promise for remote, large-scale detection of catchment-scale thaw impacts from space.

Seasonal dynamics of dissolved organic matter in the Mackenzie Delta, Canadian Arctic waters: Implications for ocean colour remote sensing

Increasing air temperatures and associated permafrost thaw in Arctic river watersheds, such as the Mackenzie River catchment, are directly affecting the aquatic environment. As a consequence, the quantity and the quality of dissolved organic carbon (DOC) that is transported via the Mackenzie River into the Arctic Ocean is expected to change. Particularly in these remote permafrost regions of the Arctic, monitoring of terrigenous organic carbon fluxes is insufficient and knowledge of distribution and fate of organic carbon when released to the coastal waters is remarkably lacking. Despite its poorly evaluated performance in Arctic coastal waters, Satellite Ocean Colour Remote Sensing (SOCRS) remains a powerful tool to complement monitoring of land-ocean DOC fluxes, detect their trends, and help in understanding their propagation in the Arctic Ocean.In this study, we use in situ and SOCRS data to show the strong seasonal dynamics of the Mackenzie River plume and the spatial distribution of associated terrigenous DOC on the Beaufort Sea Shelf for the first time. Using a dataset collected during an extensive field campaign in 2019, the performance of three commonly-used atmospheric correction (AC) algorithms and two available colored dissolved organic matter (CDOM) retrieval algorithms were evaluated using the Ocean and Land Colour Instrument (OLCI). Our results showed that in optically-complex Arctic coastal waters the Polymer AC algorithm performed the best. For the retrieval of CDOM, the gsmA algorithm (Mean Percentage Error (MPE) = 35.7%) showed slightly more consistent results compared to the ONNS algorithm (MPE = 37.9%). By merging our measurements with published datasets, the newly-established DOC-CDOM relationship for the Mackenzie-Beaufort Sea region allowed estimations of DOC concentrations from SOCRS across the entire fluvial-marine transition zone with an MPE of 20.5%. Finally, we applied SOCRS with data from the Sentinel-3 OLCI sensor to illustrate the seasonal variation of DOC concentrations in the surface waters of the Beaufort Sea on a large spatial scales and high frequency throughout the entire open water period. Highest DOC concentrations and largest lateral extent of the plume were observed in spring right after the Mackenzie River ice break-up indicating that the freshet was the main driver of plume propagation and DOC distribution on the shelf. Satellite-derived images of surface water DOC concentration placed the in situ observations into a larger temporal and spatial context and revealed a strong seasonal variability in transport pathways of DOC in the Mackenzie- Beaufort Sea region.

Terrigenous organic carbon drives methane dynamics in cascade reservoirs in the upper Yangtze China

Methane (CH4) emissions from freshwaters to the atmosphere have a profound impact on global atmospheric greenhouse gas (GHG) concentrations. Anthropogenic footprints such as dam construction and reservoir operation significantly changed the fate and transport of CH4 in freshwaters. The source of particulate organic carbon (POC) in reservoirs is a critical factor controlling CH4 production and emissions. However, little is known of how reservoir operation mediates the transport of POC and regulates CH4 accumulation in cascade hydroelectric reservoirs. Here, spatial and temporal variations in POC and CH4 were explored in the Xiluodu (XLD) and Xiangjiaba (XJB) reservoirs which are deep valley cascade reservoirs located in the main channel of the upper Yangtze River. Based on the δ13C-POC and N/C mole ratio of particulate organic matter, the results of multi-endmember stable isotope mixing models by a Bayesian model showed that terrigenous POC and autochthonous POC accounted for approximately 55% ± 18% and 43% ± 19% (SD, n = 179) of POC, respectively. Together with other hydrological and environmental parameters, we found that the input of terrigenous POC was dominantly influenced by water level variations and flow regulation due to reservoir operation. The cumulative effect of POC caused by cascade dams was not apparent. Terrigenous POC were more likely to drive CH4 accumulation in our study. Evident low level of CH4 in both reservoirs were likely affected by low sedimentation of POC and microbial CH4 oxidation. We hope our study could provide a conceptual framework for further modeling of CH4 dynamics in cascade reservoirs.

Seasonal Changes of Organic Carbon Mixing, Degradation and Deposition in Yangtze River Dominated Margin Related to Intrinsic Molecular and External Environmental Factors

AbstractThe East Asian monsoon is characterized by warm, humid summer and cool, dry winter that results in seasonal changes in fluvial sediment and organic carbon (OC) discharge. Here, we report measurements of elemental, isotopic, and optical compositions of OC in surface waters and sediments that were collected along the lower Yangtze River, Estuary, and East China Sea continuum in March and July 2019. The principal component analysis separates samples into three groups that correspond to fresh water area, mixing area, and seawater area. The terrigenous signal in the mixing area, indicated by water salinity and δ13C, is stronger in July. The applications of binary mixing models based on water salinity, dissolved OC (DOC) concentration and specific terrigenous fluorescence component suggest: (a) net removal of DOC from waters in July, but net addition of DOC into waters in March, attributed to more extensive degradation and larger deposition of OC in summer; and (b) more conservative behaviors of terrigenous OC compared to marine or mixed OC, suggesting an important role of intrinsic molecular characteristics on the persistence of DOC. The estimated monthly OC burial flux in the estuary and continent shelf is 0.48 × 1012 g in July and 0.081 × 1012 g of OC in March, equal to 15.5% and 2.6% of the annual OC discharge by the Yangtze River, respectively. Our study suggests that the burial of OC mainly occurs in the summer monsoon due to the larger sediment load of the Yangtze River, prevailing southeastern wind, and intensified Kuroshio Current.

Increased petrogenic and biospheric organic carbon burial in sub‐Antarctic fjord sediments in response to recent glacier retreat

AbstractFjords are recognized as hotspots of organic carbon (OC) burial in the coastal ocean. In fjords with glaciated catchments, glacier discharge carries large amounts of suspended matter. This sedimentary load includes OC from bedrock and terrigenous sources (modern vegetation, peat, soil deposits), which is either buried in the fjord or remineralized during export, acting as a potential source of CO2 to the atmosphere. In sub‐Antarctic South Georgia, fjord‐terminating glaciers have been retreating during the past decades, likely as a response to changing climate conditions. We determine sources of OC in surface sediments of Cumberland Bay, South Georgia, using lipid biomarkers and the bulk 14C isotopic composition, and quantify OC burial at present and for the time period of documented glacier retreat (between 1958 and 2017). Petrogenic OC is the dominant type of OC in proximity to the present‐day calving fronts (60.4 ± 1.4% to 73.8 ± 2.6%) and decreases to 14.0 ± 2.7% outside the fjord, indicating that petrogenic OC is effectively buried in the fjord. Beside of marine OC, terrigenous OC comprises 2.7 ± 0.5% to 7.9 ± 5.9% and is mostly derived from modern plants and Holocene peat and soil deposits that are eroded along the flanks of the fjord, rather than released by the retreating fjord glaciers. We estimate that the retreat of tidewater glaciers between 1958 and 2017 led to an increase in petrogenic carbon accumulation of 22% in Cumberland West Bay and 6.5% in Cumberland East Bay, suggesting that successive glacier retreat does not only release petrogenic OC into the fjord, but also increases the capacity of OC burial.

Influence of Riverine Discharge and Timing of Ice Retreat on Particle Sedimentation Patterns on the Laptev Sea Shelf

AbstractWe studied the influence of river discharge and timing of ice retreat on sinking fluxes of total particulate matter and its components in the Laptev Sea in August–September 2017 and 2018. Vertical fluxes were measured with short‐term sediment traps located on the shelf adjusted to the Lena and Khatanga Rivers inflows (four shallow stations in 2017) and in Vilkitski Strait/Trough area (two deeper stations) in 2018. One station outside the Khatanga plume was repeated in both years. The effect of river discharge manifested by high total particle flux (1–1.6 g m−2 d−1), high Si (0.3 g m−2 d−1) and Al (0.1 g m−2 d−1) fluxes, a high proportion of terrigenous organic carbon (10.7%–27.5% total organic carbon) was clearly recognizable only in the shelf area closest to the Lena inflow. Large contribution of the lithogenic matter to the flux on the Laptev shelf is suggested to result also from sediment resuspension (caused by the tidal mixing and upwelling events), lateral offshore transport of sediment just above the seabed, and coastal abrasion. The magnitude of vertical fluxes of total particulate matter and organic carbon was two to three times higher in 2017 (late ice retreat) than in 2018 (early ice retreat). Centric diatoms dominated protist flux in 2017 while in 2018, dinoflagellates and tintinnids dominated. The contribution of protists to the biogenic organic carbon flux reached 62% in 2018 versus &lt;1% in 2017. Zooplankton fecal pellet flux was not influenced by river discharge but was higher soon after ice melt.

Contrasting Estuarine Processing of Dissolved Organic Matter Derived From Natural and Human‐Impacted Landscapes

AbstractThe flux of terrigenous organic carbon through estuaries is an important and changing, yet poorly understood, component of the global carbon cycle. Using dissolved organic carbon (DOC) and fluorescence data from 13 British estuaries draining catchments with highly variable land uses, we show that land use strongly influences the fate of DOC across the land ocean transition via its influence on the composition and lability of the constituent dissolved organic matter (DOM). In estuaries draining peatland‐dominated catchments, DOC was highly correlated with biologically refractory “humic‐like” terrigenous material which tended to be conservatively transported along the salinity gradient. In contrast, there was a weaker correlation between DOC and DOM components within estuaries draining catchments with a high degree of human impact, that is, relatively larger percentage of arable and (sub)urban land uses. These arable and (sub)urban estuaries contain a high fraction of bioavailable “protein‐like” material that behaved nonconservatively, with both DOC removals and additions occurring. In general, estuaries draining catchments with a high percentage of peatland (≥18%) have higher area‐specific estuarine exports of DOC (&gt;13 g C m−2 yr−1) compared to those estuaries draining catchments with a high percentage (≥46%) of arable and (sub)urban land uses (&lt;2.1 g C m−2 yr−1). Our data indicate that these arable and (sub)urban estuaries tend to export, on average, ∼50% more DOC to coastal areas than they receive from rivers due to net anthropogenic derived organic matter inputs within the estuary.

Organic Carbon Burial in the Aral Sea of Central Asia

The burial of organic carbon in lake sediments plays an important role in the terrestrial carbon cycle. Clarifying the current status of carbon burial in the lakes of Central Asia is of great significance for the application of carbon balance assessments. With the analysis of the total organic carbon and nitrogen and the carbon isotope and organic carbon burial rate in the core sediment of the North Aral Sea, the status and influencing factors of organic carbon burial over the past 70 years can be revealed. The results showed that the main source of organic carbon was predominantly from lacustrine aquatic plants. However, the contribution of terrigenous organic carbon increased from the 1950s to the 1960s. The burial rate of organic carbon in North Aral Sea sediments was consistent with the overall change in the regional temperature. The burial rate of organic carbon showed an upward trend as a whole with an average of 28.78 g·m−2·a−1. Since 2010, the burial rate of organic carbon has stood at the highest level in nearly 70 years, with an average of 55.66 g·m−2·a−1. The protection of a lake by human beings can not only significantly improve the lake’s aquatic ecosystem but also help to increase the burial rate of the lake’s organic carbon.

Fate of terrigenous organic carbon in muddy clinothems on continental shelves revealed by stratal geometries: Insight from the Adriatic sedimentary archive

Continental shelves host 90% of modern Organic Carbon (OC) burial and play a key role in the sequestration of terrigenous OC over geological timescales. The efficiency of OC burial in these systems, however, varies greatly depending on the duration of exposure to oxic-suboxic conditions during sediment transport. In this study, we use observations across a wide range of stratigraphic and sedimentological scales coupled with geochemistry data from muddy shelf deposits along the western Adriatic to investigate the relation between sediment transport and burial of terrigenous (land-derived) fraction of OC (OCTerr). Our analysis focused on the Little Ice Age (LIA, 1500–1850 CE) interval, which was characterized by wet, cold, and stormy weather conditions, before the time of widespread regulation and damming of rivers. On the Adriatic shelf, LIA deposits are organized as clinothem: strata that dip gently seawards. The LIA clinothem becomes progressively steeper and deeper from north to south. Basin-scale seismic-stratigraphic analysis and biogeochemical data show evidence of elongated stratal units associated with low OCTerr content in the northern sector of the LIA clinothem, whereas farther south, where clinoforms are steeper, the LIA clinothem exhibits wavy stratal units with limited cross-shelf continuity and high OCTerr concentrations. Based on these data we infer two contrasting scenarios for OCTerr deposition during the LIA: 1) protracted sediment redistribution under the influence of coastal currents with efficient OCTerr degradation prior to final burial in the northern sector; and (2) rapid deposition of OCTerr-rich event beds as a result of flood-driven hyperpycnal flows with limited dispersion across the shelf in the southern sector. The latter scenario of deposition resulted in scattered hot spots of OCTerr burial along the apparently homogeneous western Adriatic shelf deposit. Our work documents significant lateral variability of a fine-grained system in which hot spots of OCTerr can be preserved in scattered prodelta bedsets (<1 km in across-shelf lateral continuity) over a 600 km long shelf. Shelfal clinothems worldwide should not be considered as homogeneous pools of OCTerr because of the influence of river, storm, and oceanic currents.

CASCADE – The Circum-Arctic Sediment CArbon DatabasE

Abstract. Biogeochemical cycling in the semi-enclosed Arctic Ocean is strongly influenced by land–ocean transport of carbon and other elements and is vulnerable to environmental and climate changes. Sediments of the Arctic Ocean are an important part of biogeochemical cycling in the Arctic and provide the opportunity to study present and historical input and the fate of organic matter (e.g., through permafrost thawing). Comprehensive sedimentary records are required to compare differences between the Arctic regions and to study Arctic biogeochemical budgets. To this end, the Circum-Arctic Sediment CArbon DatabasE (CASCADE) was established to curate data primarily on concentrations of organic carbon (OC) and OC isotopes (δ13C, Δ14C) yet also on total N (TN) as well as terrigenous biomarkers and other sediment geochemical and physical properties. This new database builds on the published literature and earlier unpublished records through an extensive international community collaboration. This paper describes the establishment, structure and current status of CASCADE. The first public version includes OC concentrations in surface sediments at 4244 oceanographic stations including 2317 with TN concentrations, 1555 with δ13C-OC values and 268 with Δ14C-OC values and 653 records with quantified terrigenous biomarkers (high-molecular-weight n-alkanes, n-alkanoic acids and lignin phenols). CASCADE also includes data from 326 sediment cores, retrieved by shallow box or multi-coring, deep gravity/piston coring, or sea-bottom drilling. The comprehensive dataset reveals large-scale features of both OC content and OC sources between the shelf sea recipients. This offers insight into release of pre-aged terrigenous OC to the East Siberian Arctic shelf and younger terrigenous OC to the Kara Sea. Circum-Arctic sediments thereby reveal patterns of terrestrial OC remobilization and provide clues about thawing of permafrost. CASCADE enables synoptic analysis of OC in Arctic Ocean sediments and facilitates a wide array of future empirical and modeling studies of the Arctic carbon cycle. The database is openly and freely available online (https://doi.org/10.17043/cascade; Martens et al., 2021), is provided in various machine-readable data formats (data tables, GIS shapefile, GIS raster), and also provides ways for contributing data for future CASCADE versions. We will continuously update CASCADE with newly published and contributed data over the foreseeable future as part of the database management of the Bolin Centre for Climate Research at Stockholm University.

Extensive Remineralization of Peatland‐Derived Dissolved Organic Carbon and Ocean Acidification in the Sunda Shelf Sea, Southeast Asia

AbstractSoutheast Asia is a hotspot of riverine export of terrigenous organic carbon to the ocean, accounting for ∼10% of the global land‐to‐ocean riverine flux of terrigenous dissolved organic carbon (tDOC). While anthropogenic disturbance is thought to have increased the tDOC loss from peatlands in Southeast Asia, the fate of this tDOC in the marine environment and the potential impacts of its remineralization on coastal ecosystems remain poorly understood. We collected a multi‐year biogeochemical time series in the central Sunda Shelf (Singapore Strait), where the seasonal reversal of ocean currents delivers water masses from the South China Sea first before (during Northeast Monsoon) and then after (during Southwest Monsoon) they have mixed with run‐off from peatlands on Sumatra. The concentration and stable isotope composition of DOC, and colored dissolved organic matter spectra, reveal a large input of tDOC to our site during Southwest Monsoon. Using isotope mass balance calculations, we show that 60%–70% of the original tDOC input is remineralized in the coastal waters of the Sunda Shelf, causing seasonal acidification. The persistent CO2 oversaturation drives a CO2 efflux of 2.4–4.9 mol m−2 yr−1 from the Singapore Strait, suggesting that a large proportion of the remineralized peatland tDOC is ultimately emitted to the atmosphere. However, incubation experiments show that the remaining 30%–40% tDOC exhibits surprisingly low lability to microbial and photochemical degradation, suggesting that up to 20%–30% of peatland tDOC might be relatively refractory and exported to the open ocean.

Distribution, Source, and Burial of Sedimentary Organic Carbon in Kermadec and Atacama Trenches

AbstractKnowledge of sedimentary organic carbon (OC) in hadal trenches, the deepest ocean realm, is rudimentary. Here, we conducted a comprehensive analysis of total OC (TOC), stable and radio‐carbon isotopes (δ13C and Δ14C), and biomarkers (e.g., n‐alkanes, n‐alkanols and n‐fatty acids) in 12 sediment cores collected from hadal (trench axis) and non‐hadal (abyssal plains and slopes) settings of the Kermadec Trench (Southwestern Pacific) and Atacama Trench (Southeastern Pacific) regions. Our results show that the TOC in the Atacama Trench region (0.86% ± 0.69%) is significantly higher than that of the Kermadec Trench region (0.29% ± 0.08%), likely related to different surface primary productivity. In both trench regions, the hadal sites are generally characterized by more negative δ13C, higher TOC/TN ratio, and similar or higher abundance ratio of terrigenous/marine biomarkers as compared to the non‐hadal sites, suggesting the selective preservation of terrigenous biogenic/fossil OC at the hadal trench axis. The linear increase in 14C age with sediment depth in non‐hadal cores reflects steady depositional conditions, whereas seven out of eight hadal sediment cores show 14C age reversals presumably due to occasional mass‐transport deposits. Our results suggest (1) a strong heterogeneity in sedimentary OC characteristics between trenches and within each trench and (2) relatively high accumulation rates of terrigenous OC in both the Kermadec Trench (0.35 ± 0.04 g m−2 yr−1) and the Atacama Trench (1.4 ± 0.5 g m−2 yr−1). Thus, hadal trenches appear to represent an important environment for terrigenous carbon deposition in the deep ocean.