Source Of Dissolved Organic Carbon Research Articles

Optical remote sensing (Sentinel-3 OLCI) used to monitor dissolved organic carbon in the Lena River, Russia

In the past decades the Arctic has experienced stronger temperature increases than any other region globally. Shifts in hydrological regimes and accelerated permafrost thawing have been observed and are likely to increase mobilization of organic carbon and its transport through rivers into the Arctic Ocean. In order to better quantify changes to the carbon cycle, Arctic rivers such as the Lena River in Siberia need to be monitored closely. Since 2018, a sampling program provides frequent in situ observations of dissolved organic carbon (DOC) and colored dissolved organic matter (CDOM) of the Lena River. Here, we utilize this ground truth dataset and aim to test the potential of frequent satellite observations to spatially and temporally complement and expand these observations. We explored all available overpasses (~3250) of the Ocean and Land Colour Instrument (OLCI) on Sentinel-3 within the ice-free periods (May – October) for four years (2018 to 2021) to develop a new retrieval scheme to derive concentrations of DOC. OLCI observations with a spatial resolution of ~300 m were corrected for atmospheric effects using the Polymer algorithm. The results of this study show that using this new retrieval, remotely sensed DOC concentrations agree well with in situ DOC concentrations (MAPD=10.89%, RMSE=1.55 mg L−1, r²=0.92, n=489). The high revisit frequency and wide swath of OLCI allow it to capture the entire range of DOC concentrations and their seasonal variability. Estimated satellite-derived DOC export fluxes integrated over the ice-free periods of 2018 to 2021 show a high interannual variability and agree well with flux estimates from in situ data (RMSD=0.186 Tg C, MAPD=4.05%). In addition, 10-day OLCI composites covering the entire Lena River catchment revealed increasing DOC concentration and local sources of DOC along the Lena from south to north. We conclude that moderate resolution satellite imagers such as OLCI are very capable of observing DOC concentrations in large/wide rivers such as the Lena River despite the relatively coarse spatial resolution. The global coverage of remote sensing offers the expansion to more rivers in order to improve our understanding of the land-ocean carbon fluxes in a changing climate.

Extreme storm events shift DOC export from transport-limited to source-limited in a typical flash flood catchment

Dissolved organic carbon (DOC) export regimes are co-determined by DOC source supply and hydrological transport. Field studies have indicated that catchment DOC export is a single regime (source- or transport-limited, or chemostatic). If a shift between DOC export regimes exists, as has been rarely reported before based on low-frequency observation, then conceptual paradigms regarding lateral carbon export need to be revised. DOC dynamics of a flash flood catchment were investigated in this study with high-frequency observations during flood seasons. A three-phase DOC concentration and discharge relationship (n = 713) was observed, i.e., slow increase, rapid increase, and flat phases that occurred during the inter-storm, moderate storm, and extreme storm periods, respectively. Further hysteresis analysis showed that the anticlockwise pattern observed during moderate storms shifted to a clockwise pattern during extreme storms. These transitions suggest that extreme storm events shifted DOC export from transport-limited to source-limited. Failure to consider such a shift can cause significant overestimation of DOC yield in flash flood catchments where DOC yield is largely driven by storms.

Investigating hydrological transport pathways of dissolved organic carbon in cold region watershed based on a watershed biogeochemical model

Dissolved organic carbon (DOC) is a significant component of regional and global carbon cycles and an important surface water quality indicator. DOC affects the processes of solubility, bioavailability and transport for a number of contaminants, such as heavy metals. Therefore, it is crucial to understand DOC fate and transport in the watershed and the transport pathways of DOC load. We modified a previously developed watershed-scale organic carbon model by incorporating the DOC load from glacier melt runoff and used the modified model to simulate periodic daily DOC load in the upper Athabasca River Basin (ARB) in the cold region of western Canada. The calibrated model achieved an overall acceptable performance for simulating daily DOC load with model uncertainties mainly from the underestimation of peak loads. Parameter sensitivity analysis indicates that the fate and transport of DOC load in upper ARB are mainly controlled by DOC production in the soil layers, DOC transport at the soil surface, and reactions in the stream system. The modeling results indicated that the DOC load is mainly from the terrestrial sources and the stream system was a negligible sink in the upper ARB. It also indicated that rainfall-induced surface runoff was the major transport pathway of DOC load in the upper ARB. However, the DOC loads transported by glacier melt runoff were negligible and only accounted for 0.02% of the total DOC loads. In addition, snowmelt-induced surface runoff and lateral flow contributed 18.7% of total DOC load, which is comparable to the contribution from the groundwater flow. Our study investigated the DOC dynamics and sources in the cold region watershed in western Canada and quantified the contribution of different hydrological pathways to DOC load, which could provide a useful reference and insight for understanding watershed-scale carbon cycle processes.

Groundwater flow paths drive longitudinal patterns of stream dissolved organic carbon (DOC) concentrations in boreal landscapes

Abstract. Preferential groundwater flow paths can influence dissolved organic carbon (DOC) concentration and export in the fluvial network because they facilitate the inflow of terrestrial DOC from large upslope contributing areas to discrete sections of the stream, referred to as discrete riparian inflow points (DRIPs). However, the mechanisms by which DRIPs influence longitudinal patterns of stream DOC concentrations are still poorly understood. In this study, we ask how DRIPs affect longitudinal patterns of stream DOC concentrations under different hydrologic conditions, as they can simultaneously act as major sources of terrestrial DOC and important locations for in-stream processes. To answer this question, we tested four model structures that account for different representations of hydrology (distributed inflows of DRIPs vs. diffuse groundwater inflow) and in-stream processes (no DOC uptake vs. in-stream DOC uptake downstream of DRIPs) to simulate stream DOC concentrations along a 1.5 km headwater reach for 14 sampling campaigns with flow conditions ranging from droughts to floods. Despite the magnitude and longitudinal patterns of stream DOC concentration varying across campaigns, at least one model structure was able to capture longitudinal trends during each campaign. Specifically, our results showed that during snowmelt periods or high-flow conditions (>50 L s−1), accounting for distributed inputs of DRIPs improved simulations of stream DOC concentrations along the reach, because groundwater inputs from DRIPs diluted the DOC in transport. Moreover, accounting for in-stream DOC uptake immediately downstream of DRIPs improved simulations during five sampling campaigns that were performed during spring and summer, indicating that these locations served as a resource of DOC for aquatic biota. These results show that the role of DRIPs in modulating DOC concentration, cycling, and export varies over time and depends strongly on catchment hydrology. Therefore, accounting for DRIPs can improve stream biogeochemistry frameworks and help inform management of riparian areas under current and future climatic conditions.

Response of dissolved organic carbon in rainwater during extreme rainfall period in megacity: Status, potential source, and deposition flux

Air pollution and related wet deposition process (rainfall) caused environmental hazards under the climate change, particularly in urban regions, attracting global concern and challenges. Atmospheric dissolved organic carbon (DOC) deposition is not only the major removal pathway of OC from atmosphere, but also a significant influence factor of urban haze pollution and local climate. Although the significance of DOC deposition to carbon budgets is confirmed, the extreme rainfall influenced OC transfers from the atmosphere to land is poorly understood. This study systematically investigated the rainwater DOC in Beijing during the extreme rainfall period of 2021 to explore its status, source, and flux. The results showed that the rainwater DOC concentration level is close to the Asian and global mean level, while the DOC deposition flux was relatively high due to high rainfall amount and rainfall scouring, and the overall declined trend of DOC concentrations was identified. Source identification revealed that human OC emissions (municipal wastes, agricultural and traffic emission) are the primary sources of DOC, whereas ocean and crust source contributed negligibly. This research clarified the extreme rainfall-driven rainwater DOC dynamics in a megacity and supported the evaluation of global carbon budgets.

Seasonal and tidal controls of the quantity and quality of dissolved organic matter at the marsh creek-estuarine interface

Tidal marshes are an important source of dissolved organic matter (DOM) to estuaries, and DOM plays an integral role in regulating water quality and health of coastal ecosystems. However, our understanding of temporal patterns of DOM quantity and composition at the marsh-estuarine interface is limited. This study investigated temporal changes in colored DOM (CDOM), an important component of dissolved organic carbon (DOC), exchanged across a brackish marsh-estuarine system. The sources of DOC were examined using stable carbon isotope values whereas the sources of CDOM were based on spectroscopic properties, including absorbance and fluorescence excitation-emission matrices (EEMs). Samplings at the Taskinas marsh creek-interface in Virginia (USA) captured a range of tidal stages, seasons, and environmental conditions over a three-year timeseries. Water from low and high tides was used to represent marsh and estuarine endmembers, respectively. Absorbance of CDOM at 440 nm ranged from 0.83 to 6.75 m-1, and the highest values were found during low tides (mean 2.78 ± 0.21 m −1). EEMs were composed of three humic-like components (C1, C2, C3) and one protein-like component (C4). Generally, the terrestrial humic-like (C1) and marine humic-like (C2) components were more abundant than other measured components. Seasonally, CDOM absorbance was highest in spring and summer. Contributions of CDOM from terrestrial sources increased in spring during periods of high runoff and peaked in summer during periods of high marsh productivity. Higher contributions of terrestrially derived CDOM were also measured in fall during periods of plant senescence. The aquatic component (C4) was higher during periods of increased phytoplankton production and during periods of high microbial respiration of terrestrial and planktonic organic matter. Although the amount of marsh exported CDOM varied with season, its composition varied considerably less, especially with respect to autochthonous CDOM. In a focused study in 2018, inferences about the terrestrial versus estuarine sources of CDOM were compared to source inferences made using measurements of stable carbon isotopes (δ13C) of DOC and DIC. δ13CDOC values ranged from −32.25 to −25.91‰, indicative of wetland organic matter and humic-like DOM; δ13CDIC ranged from −9.69 to −3.12‰, consistent with groundwater and estuarine sources. Overall, CDOM and stable isotope measurements indicate that humic materials were the primary source of DOM at this marsh-estuarine interface, including inputs from marsh plants and soils and products from microbial degradation of marsh and terrestrial materials, with lesser contributions from aquatic sources.

Free Versus Bound Concentration: Passive Dosing from Polymer Meshes Elucidates Drivers of Toxicity in Aquatic Tests with Benthic Invertebrates.

Aquatic toxicity tests with benthic organisms are used to predict the toxicity of hydrophobic organic chemicals (HOCs) in sediments, assuming that the freely dissolved concentration (Cfree ) is a good surrogate of bioavailability in the exposure system. However, Cfree of HOCs is difficult to control in water-only setups. Moreover, the role of dissolved organic carbon (DOC) in the occurrence of toxicity needs clarification because DOC concentrations in sediment porewater can be substantially higher than in typical test water. We introduced biocompatible polyethylene meshes with high sorptive capacities and fast release kinetics as a novel passive dosing phase, which maintained Cfree and Cwater (i.e., free + DOC-bound) in Hyalella azteca water-only tests. Adding the supernatant fraction of peat to test water as a DOC source increased Cwater to an extent comparable to sediment porewater and significantly increased and decreased the observed toxicity of permethrin and benzo[a]pyrene, respectively, to H. azteca. This result indicates that DOC can both benefit and harm test species likely due to the increased health after ingestion of DOC and to the uptake of DOC-bound HOCs, respectively. Passive dosing in combination with the addition of sediment DOC surrogates may better reflect exposure and habitat conditions in sediment porewater than conventional aquatic tests. Environ Toxicol Chem 2022;00:1-10. © 2022 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.

Origin of dissolved organic carbon under phosphorus-limited coastal-bay conditions revealed by fluorescent dissolved organic matter

To determine the origins of dissolved organic carbon (DOC) in a bay of volcanic Jeju Island, where the discharge of fresh groundwater (FGW) is dominant, we measured fluorescent dissolved organic matter (FDOM) and implemented a parallel factor analysis (PARAFAC). The PARAFAC model identified three humic-like components (FDOMH) and one protein-like component (FDOMP). DOC was extremely deficient in the FGW (35 ± 13 μM) and positively correlated with salinity in the coastal environment, indicating oceanic DOC contribution. The FDOMP pattern was similar to that of DOC, suggesting that marine biological production is a primary DOC source in this region. Particularly, significant FDOMP correlations in the coastal waters with the fluxes of dissolved inorganic phosphorus (DIP; R2 = 0.31) and dissolved silicon (R2 = 0.46) from the FGW demonstrated that in situ biological production is facilitated by FGW-borne nutrient addition. However, the absence of a correlation between the fluxes of dissolved inorganic nitrogen (DIN) and FDOMP (R2 <0.01) indicated that anthropogenic DIN is not essential for DOC production under the P-limited nutrient conditions and diatom-dominant conditions prevailing on the coastal Jeju Island. Here, we calculated the potential capacity of carbon fixation by marine biological activity based on the Redfield ratio of carbon and phosphorus with DIP fluxes. The flux accounts for approximately 2% of the terrestrial carbon uptake in South Korea. Therefore, optical properties of FDOM may be good indicators of coastal DOC origin, and nutrient speciation may be linked to the carbon cycle.

Seasonal and spatial variations in riverine DOC exports in permafrost-dominated Arctic river basins

• Seasonality of riverine DOC exports is strongly associated with hydrological regimes. • The extent and degradation of permafrost regulate riverine DOC mobilization. • Water temperature is an important factor influencing riverine DOC exports. Climate warming is accelerating the release of voluminous organic carbon from thawing permafrost into the Arctic Ocean via riverine transport. However, the seasonal variations in riverine dissolved organic carbon ( DOC ) exports in Arctic river basins with different areal extents of permafrost and how changes in water temperature ( T w ) impact seasonal DOC exports are not fully understood. In this study, the concentrations, ages and seasonality of riverine DOC in the estuaries of six major Arctic rivers (Ob, Yenisei, Lena, Kolyma, Yukon and Mackenzie) were analysed using Arctic Great Rivers Observatory (ArcticGRO) datasets from 2003 to 2019. The results showed that DOC concentrations generally increased with the increases in the streamflow, but always dropped to the minimum with the oldest Δ 14 C-DOC ages (as old as 1650 years BP) in the freezing period (November–April), when the streamflow originates predominantly from groundwater. During the flood pulse period (May or June), a rapid increase in riverine DOC concentration with younger organic carbon (Δ 14 C values from −61 to 152‰) was observed, likely associated with snowmelt-dominated runoff regimes (lower δ 18 O-H 2 O of approximately −20.4 ± 1.6‰). During the ice-free period (June–September), DOC concentrations decreased due to the enhanced dilution of streamflow from precipitation. In the Lena and Kolyma River basins with large areal extents of continuous permafrost, over 70% of DOC flux exported during the ice-free period originated from DOC sources from ∼410 years and ∼230 years BP to the present, respectively; this suggests that greater permafrost extents restrict the release of older DOC into rivers. However, riverine DOC exports likely respond positively to changes in T w during the ice-free period. In addition, such a positive response is likely to be enhanced in basins with larger percentages of sporadic permafrost, thicker active layers, more precipitation and less soil organic carbon. Ultimately, under a warming climate, riverine DOC exports are expected to rise with increasing river water temperatures.

Photosensitizing properties of dissolved organic carbon in Canadian prairie pothole wetland ponds change in response to sunlight

Dissolved organic carbon (DOC) is an important component of the global carbon cycle providing ecological services such as carbon sources for microorganisms and the provision of a protective barrier between ultraviolet radiation and aquatic organisms. Our study examined the impacts of photodegradation on the optical properties of DOC in prairie wetland ponds in central Saskatchewan, Canada. Surface water was collected from two ponds with seasonal average DOC concentrations of 71.1 mg L−1 (More-DOC Pond) and 32.7 mg L−1 (Less-DOC Pond) and filtered through 1.2 µm GF/Fs into Teflon bottles transparent to UV light. Samples divided into dark and light treatments were incubated in situ at three different depths (surface, 0.25m, and 0.5 m) and collected every 2 weeks for 4 months. Excitation emission matrix scans from 300 to 800 nm and absorbance at 254 nm were measured. Absorbance at 254 nm in the More-DOC Pond and Less-DOC Pond waters decreased by 34% and 50%, respectively. Two fluorescence components were identified corresponding to previous published peaks C and M. Although bulk DOC concentrations did not show significant differences over time, fluorescence intensity of peak C decreased by 39% and 47%, and of peak M increased by 19% and 29%, in the More-DOC Pond and Less-DOC Pond, respectively. Increases in other fluorescence indicators such as fluorescence index (35% and 22%) and FRESH (29% and 30%) were also observed. Overall, terrestrial DOC from our sampling ponds became less aromatic, more aliphatic, of lower molecular weight, and lost absorptivity and fluorescence intensity after 12 weeks of incubation. Results of this study will provide a better understanding of optical characterizations and sources of DOC, and act as a foundation to further study on the role of DOC in prairie wetland ponds.

Groundwater travel times predict DOC in streams and riparian soils across a heterogeneous boreal landscape

Dissolved organic carbon (DOC) in surface waters is an important component of the boreal landscape carbon budget and a critical variable in water quality. A dominant terrestrial DOC source in the boreal landscape is the riparian zone. These near stream areas play a key role in regulating DOC transport between land and aquatic ecosystems. The groundwater dynamics at this interface have been considered a major controlling variable for DOC export to streams. This study focuses on the regulating role of groundwater levels and mean travel times (MTT) on riparian DOC concentrations and, subsequently, stream DOC. This is done by comparing them as explanatory variables to capture the spatial and intra-annual variability of the stream and riparian groundwater DOC. We used a physically based 3D hydrological model, Mike SHE, to simulate DOC concentrations of the riparian zones for 14 sub-catchments within the Krycklan catchment (Sweden). The model concept assumes that DOC concentrations will be higher in groundwater moving through shallow flow paths. In the model, this can be linked to the position of the groundwater table at a point of observation or the travel time, which will generally be shorter for water that has travelled through shallow and more conductive soil layers. We compared the results with both observed stream and groundwater concentrations. The analysis revealed that the correlation between modelled and observed annual averages of stream DOC increased from r = 0.08 to r = 0.87 by using MTT instead of groundwater level. MTT also better captured the observed spatial variability in riparian DOC concentrations and more successfully represented seasonal variability of stream DOC. We, therefore, suggest that MTT is a better predictor than groundwater level for riparian DOC concentration because it can capture a greater variety of catchment heterogeneities, such as variation in soil properties, catchment size, and input from deep groundwater sources.

Quantification of the carbon released by a marine fish using a carbon release model and radiocarbon

Here we propose a carbon release model that divides fish-released carbon into two sources (ingested food and the fish body), and three forms (dissolved organic carbon (DOC), CO2, and particulate carbon (PC)). We quantified the daily carbon budget of a marine fish Oryzias melastigma by feeding the fish radiocarbon-labeled living rotifer. We found that 91%–92%, 25%–47%, 28%–50%, 20%–31%, and 8%–9% of the ingested food carbon was absorbed, assimilated, and released as DOC, CO2, and PC, respectively. Fish body carbon dissimilated/catabolized and released as 0.053–0.12 d−1 at two daily food rations. DOC, CO2, and PC accounted for 39%–42%, 39%–45%, and 16%–19% of the released fish body carbon, respectively. Our study shows that the fish transformed substantial fractions of their daily ingested food and dissimilated body carbon into DOC, and fish may be an important source of DOC in the ocean.

Spatial Distributions of Riverine and Marine Dissolved Organic Carbon in the Western Arctic Ocean: Results From the 2018 Korean Expedition

AbstractSeasonal primary production and river discharge increases in the Arctic Ocean exert a significant influence on the dissolved organic carbon (DOC) cycle. To improve our knowledge of the spatial heterogeneity of DOC source and concentration in the rapidly changing Arctic Ocean, we investigated the distributions of riverine and marine DOC in the western Arctic Ocean during the summer of 2018. Although the surface bulk DOC concentration indicated no clear distinction in its distribution between the Chukchi Borderland (CBL)/northern Chukchi Sea (NCS) and East Siberian Sea (ESS)/Mendeleyev Ridge (MR) regions, the estimated riverine DOC concentration (28 ± 4.2 μM C) and its contribution (40 ± 5.7%) in the surface layer of the CBL/NCS region were higher than those (19 ± 5.6 μM C and 26 ± 8.5%) in the ESS/MR region, which was attributed to the accumulation of freshwater, strong stratification, and a longer residence time in the CBL/NCS region. In contrast, although marine DOC was the dominant DOC component in both the CBL/NCS and ESS/MR regions, the higher marine DOC concentration (54 ± 8.1 μM C) and its contribution (73 ± 8.2%) in the East Siberian shelf/slope region were consistent with high bacterial abundance, which was associated with extremely high surface phytoplankton blooms sustained by nutrient supply from the deep layer, suggesting that the supply of bioavailable DOC resulted in active bacterial activities. Overall, the spatial differences in water properties between the two regions had large influences on the regional distributions of riverine and marine DOC.

RETRACTED: Globally, Freshwater Ecosystems Emit More CO2 Than the Burning of Fossil Fuels

Freshwater emits substantial volumes of CO2 to the atmosphere. This has largely gone unnoticed in global carbon budgets. My aim was to quantify the CO2 emanating from freshwater from 66° N to 47° S latitudes via in situ bacterial respiration (BR). I determined BR (n = 326) as a function of water temperature. Freshwater is emitting CO2 at a rate of 58.5 Pg C y−1 (six times that of fossil fuel burning). Most is emitted from the Northern Hemisphere. This is because the high northern summer temperatures coincide with most of the world’s freshwater. Diffuse DOC sources, for example dust, may be driving high freshwater BR. However, many sources remain elusive and not individually quantified in the literature. We must include freshwater CO2 emissions in climate models. Identifying, quantifying and managing freshwater’s diffuse sources of Dissolved Organic Carbon (DOC) will hopefully provide us with another opportunity to change our current climate trajectory.

The channel‐source hypothesis: Empirical evidence for in‐channel sourcing of dissolved organic carbon to explain hysteresis in a headwater mountain stream

AbstractCatchment hydrologists have long puzzled over the question: How can catchments rapidly generate storm flows and pulses of solutes in response to storm events? Conceptual models viewing catchments as composed of discrete source areas generating flow at unique time scales and with unique chemical characteristics have been used to explain the observed changes in flow and water chemistry. Surprisingly, those conceptual models usually do not treat the stream channel as one of the potential source areas. Here, we propose the channel‐source hypothesis in which the stream itself should be considered as a potential source with the same rigour as other contributing areas. We pose this in the spirit of the scientific use of the word: a hypothesis is not a proven idea but rather a provisional supposition serving as the basis for further study. We suggest that the channel should be considered as a potential source for dissolved organic carbon (DOC). Channels store substantial amounts of organic matter, and stream ecologists have long studied stream carbon cycling. From those studies, we know that leaching and decomposition can generate DOC from particulate organic carbon (POC). Further, POC is stored in channel ‘dead‐zones’—regions of low flow velocity ‐ that can be activated as flow velocity increases, thus releasing accumulated DOC during storms. All catchments are different; there is no reason to assume that channel sources are always important, in every catchment, in every storm. Thus, the channel‐source hypothesis does not replace existing conceptual models. Instead, it adds another potential mechanism that may explain DOC dynamics observed in streams. The channel‐source hypothesis has substantial implications for catchment studies examining sources of DOC in stream water or using DOC as a tracer to determine the locations of, and proportional contributions of, different source areas for streamflow generation.

Dissolved Organic Carbon (DOC) in Ground Ice on Northeastern Tibetan Plateau

Ground ice in permafrost stores substantial amounts of dissolved organic carbon (DOC) upon thaw, which may perpetuate a carbon feedback in permafrost regions, yet little is known to date about the dynamics of DOC and source variability of ground ice on the Tibetan Plateau. Here, the high-resolution data of DOC in ground ice (4.8 m in depth) from two permafrost profiles on the Northeastern Tibetan Plateau (NETP) were firstly presented. We quantified the DOC concentrations (mean: 9.7–21.5 mg/L) of ground ice and revealed sizeable—by a factor of 7.0–36.0—enrichment of the ground ice relative to the other water elements on the TP. Results indicated remarkable depth differences in the DOC of ground ice, suggestive of diverse sources of DOC and different sequestration processes of DOC into ice during permafrost evolution. Combined with DOC and carbon isotopes (δ13CDOC), we clarified that decomposition of soil organic matter and leaching of DOC from organic layers and surrounding permafrost sediments are the important carbon sources of ground ice. The DOC sequestration of ground ice in the upper layers was related to the active layer hydrology and freeze–thaw cycle. However, the permafrost evolution controlled the decomposition of organic carbon and sequestration of DOC in the deep layers. A conceptual model clearly illustrated the dynamics of DOC in ground ice and suggested a significant impact on the carbon cycle on the NETP. The first attempt to explore the DOC in ground ice on the NETP is important and effective for further understanding of carbon cycle under permafrost degradation on the Tibetan Plateau.

Age and chemistry of dissolved organic carbon reveal enhanced leaching of ancient labile carbon at the permafrost thaw zone

Abstract. Climate change will alter the balance between frozen and thawed conditions in Arctic systems. Increased temperatures will make the extensive northern permafrost carbon stock vulnerable to decomposition and translocation. Production, cycling, and transport of dissolved organic carbon (DOC) are crucial processes for high-latitude ecosystem carbon loss that result in considerable export off the Arctic landscape. To identify where and under what conditions permafrost DOC is mobilized in an Arctic headwater catchment, we measured radiocarbon (14C) of DOC and assessed DOC composition with ultraviolet–visible spectroscopy (UV–Vis) of surface waters and shallow and deep subsurface porewaters from 17 drainages in the Barrow Environmental Observatory in Alaska. Samples were collected in July and September 2013 to assess changes in age and chemistry of DOC over time. DOC age was highly variable ranging from modern (19 ‰ Δ14C) to approximately 7000 BP (−583 ‰ Δ14C). DOC age increased with depth, over the summer as the active layer deepened, and with increasing drainage size. DOC quality indicators reflected a DOC source rich in high molecular-weight and aromatic compounds, characteristics consistent with vegetation-derived organic matter that had undergone little microbial processing, throughout the summer and a weak relationship with DOC age. In deep porewaters, DOC age was also correlated with several biogeochemical indicators (including dissolved methane concentration, δ13C, and the apparent fractionation factor), suggesting a coupling between carbon and redox biogeochemistry influencing methane production. In the drained thawed lake basins included in this study, DOC concentrations and contributions of vegetation-derived organic matter declined with increasing basin age. The weak relationship between DOC age and chemistry and consistency in DOC chemical indicators over the summer suggest a high lability of old DOC released by thawing permafrost.

Relationships between riverine and terrestrial dissolved organic carbon: Concentration, radiocarbon signature, specific UV absorbance

The transfer of dissolved organic carbon (DOC) from land to watercourses plays a major role in the carbon cycle, and in the transport and fate of associated organic and inorganic contaminants. We investigated, at global scale, how the concentrations and properties of riverine DOC depend upon combinations of terrestrial source solutions. For topsoil, subsoil, groundwater and river solutions in different Köppen-Geiger climatic zones, we compiled published and new values of DOC concentration ([DOC]), radiocarbon signature (DO14C), and specific UV absorbance (SUVA). The average value of each DOC variable decreased significantly in magnitude from topsoil to subsoil to groundwater, permitting the terrestrial sources to be distinguished. We used the terrestrial data to simulate the riverine distributions of each variable, and also relationships between pairs of variables. To achieve good matches between observed and simulated data, it was necessary to optimise the distributions of water fractions contributed by each of the three terrestrial sources, and also to reduce the mean input terrestrial [DOC] values, to about 60% of the measured ones. One possible explanation for the required lowering of the modelled terrestrial [DOC] values might be unrepresentative sampling of terrestrial DOC, including dilution effects; another is the loss of DOC during riverine transport. High variations in simulated riverine DOC variables, which match observed data, are due predominantly to variations in source solution values, with a lesser contribution from the different combinations of source waters. On average, most DOC in rivers draining catchments with forest and/or grass-shrub land cover comes in similar amounts from topsoil and subsoil, with about 10% from groundwater. In rivers draining croplands, subsoil and groundwater solutions are the likely dominant DOC sources, while in wetland rivers most DOC is from topsoil.

Dissolved Organic Carbon Source Attribution in the Changjiang Outflow Region of the East China Sea.

The variable optical properties of chromophoric dissolved organic matter (CDOM) under the complicated dynamic marine environment make it difficult to establish a robust inversion algorithm for quantifying the dissolved organic carbon (DOC). To better understand the main factors affecting the relationship between the DOC and the CDOM when the Changjiang diluted water (CDW) interacts with the marine currents on the wide continental shelf, we measured the DOC concentration, the absorption, and the fluorescence spectra of the CDOM along the main axis and the northern boundary of the CDW. The sources of DOC and their impacts on the relationship between the optical properties of the DOC and CDOM are discussed. We reached the following conclusions: There are strong positive correlations between the absorptive and fluorescent properties of the DOC and the CDOM as a whole. The dilution of the terrestrial DOC carried by the CDW through mixing with saline sea water is the dominant mechanism controlling the characteristics of the optical properties of the CDOM. CDOM optical properties can be adopted to establish inversion models in retrieving DOC in Changjiang River Estuary. It is concluded that the introduction of extra DOC from different sources is the main factor causing the regional optical complexity leading to the bias of DOC estimation rather than removal mechanism. As whole, the input of polluted water from Huangpujiang River with abnormally high and Fs(355) will induce the overestimation of DOC. In the main axis of CDW, the impact from autochthonous DOC input to the correlation between DOC and CDOM can be neglected in comparison with conservative dilution procedure. The relationship between the DOC and the CDOM on the northern boundary of the CDW is more complicated, which can be attributed to the continuous input of terrestrial material from the Old Huanghe Delta by the Subei Coastal Current, the input of materials from the Yellow sea by the Yellow Sea Warm Western Coastal Current, and the input of materials from the Changjiang Basin by the CDW. The results of this study suggest that long-term observations of the regional variations in the DOM inputs from multiple sources in the interior of the CDW are essential, which is conducive to assess the degree of impact to the DOC estimation through the CDOM in the East China Sea.

Distribution and Dynamics of Dissolved Organic Matter in the Changjiang Estuary and Adjacent Sea

AbstractLarge, river‐dominated estuaries provide important land‐ocean interfaces for biogenic element fluxes that impact global marine biogeochemistry. However, the reactivity and fate of dissolved organic matter (DOM) in this dynamic region remain not well understood. In this study, three cruises were conducted in February, May, and July 2017 in the Changjiang Estuary and adjacent sea (CEAS). Incubation experiments to determine photochemically and/or biologically mediated degradation of terrigenous and marine DOM were performed. Dissolved organic carbon (DOC), chromophoric DOM (CDOM) absorption, and total dissolved amino acids (TDAAs) were measured. DOM photodegradation and transformation were indicated by the CDOM spectral slope (S275−295) and diagenetic state by DOC‐normalized yields of TDAA [TDAA (%DOC)]. From the river to the open sea, DOC showed non‐conservative mixing and was rapidly removed in low salinity areas. Photodegradation, biodegradation, and photoenhanced biodegradation are important DOC removal mechanisms and exhibit specific responses depending on DOC source and composition. Terrigenous DOM is vulnerable to photodegradation, while marine DOM experiences rapid biodegradation. Contrary to DOC, TDAA (%DOC) increased from the river to the nearshore and then decreased toward the open sea, indicating the contribution of fresh marine plankton production. A box model showed that the annual DOC removal of CEAS was 2.6 ± 1.9 × 106 tons. Seaward increase of ammonium (NH4‐N) was observed in the CEAS; photoammonification, biomineralization of autochthonous and allochthonous DOM are potential NH4‐N regeneration mechanisms. A model was developed to calculate surface DOC concentrations based on CDOM absorption coefficients allowing high‐resolution monitoring of DOC in the CEAS.