Dissolved Organic Carbon Distribution Research Articles

Capturing the Dynamics of Dissolved Organic Carbon (DOC) in Tidal Saltmarsh Estuaries Using Remote‐Sensing‐Informed Models

AbstractThe fluxes of dissolved organic carbon (DOC) through tidal marsh‐influenced estuaries remain poorly quantified and have been identified as a missing component in carbon‐cycle models. The extreme variability inherent to these ecosystems of the land‐ocean interface challenge our ability to capture DOC‐concentration dynamics and to calculate accurate DOC fluxes. In situ discrete and continuous measurements provide high‐quality estimates of DOC concentration, but these strategies are constrained spatially and temporally and can be costly to operate. Here, field measurements and high‐spatial‐resolution remote sensing were used to train and validate a predictive model of DOC‐concentration distributions in the Plum Island Estuary (PIE), a mesotidal saltmarsh‐influenced estuary in Massachusetts. A large set of field measurements collected between 2017 and 2023 was used to develop and validate an empirical algorithm to retrieve DOC concentration with a ±15% uncertainty from Sentinel‐2 imagery. Implementation on 141 useable images produced a 6‐year time series (2017–2023) of DOC distributions along the thalweg. Analysis of the time series helped identify river discharge, tidal water level (WL), and a marsh enhanced vegetation index 2 as predictors of DOC distribution in the estuary, and facilitated the training and validation of a simple model estimating the distribution. This simple model was able to predict DOC along the PIE thalweg within ±16% of the in situ measurements. Implementation for three years (2020–2022) illustrated how this type of remote‐sensing‐informed models can be coupled with the outputs hydrodynamic models to calculate DOC fluxes in tidal marsh‐influenced estuaries and estimate DOC export to the coastal ocean.

A self-sustaining effect induced by iron sulfide generation and reuse in pyrite-woodchip mixotrophic bioretention systems: An experimental and modeling study

Dual electron donor bioretention systems have emerged as a popular strategy to enhance dissolved nitrogen removal from stormwater runoff. Pyrite-woodchip mixotrophic bioretention systems showed a promoted and stabilized removal of dissolved nutrients under complex rainfall conditions, but the sulfate reduction process that can induce iron sulfide generation and reuse was overlooked. In this study, experiments and models were applied to investigate the effects of filler configuration and dissolved organic carbon (DOC) dissolution rate on treatment performance and iron sulfide generation in pyrite-woodchip bioretention systems. Key parameters govern that DOC dissolution and microbe-mediated processes were obtained by experiments. The water quality models that integrate one-dimensional constant flow, sorption and microbial transformation kinetics were used to predict the performance of bioretention systems. Results showed that the mixotrophic bioretention system with woodchip mixed in the vadose zone and pyrite in the saturated zone achieves a better performance in both nitrogen removal efficiency and by-product control. Comparably, woodchip and pyrite mixed in the saturated zone could encounter a high secondary pollution risk. The sensitivity coefficients of oxic/anoxic DOC dissolution rates to total nitrogen removal are 0.36 and -2.43 respectively. Iron sulfide generation was affected by DOC distribution and the competition between heterotrophic denitrifiers, autotrophic denitrifiers, and sulfate-reducing bacteria (SRB). DOC accumulation has an antagonistic effect on iron production and sulfate reduction. Extra DOC accumulation favors sulfate reduction while high DOC concentration inhibits pyrite-based denitrification and reduces Fe(III) production. The recycling of iron sulfide can improve the robustness and sustainability of bioretention systems.

Distribution and composition of redox-active species and dissolved organic carbon in Arctic lacustrine porewaters

ABSTRACT The interaction between redox-active species and dissolved organic carbon (DOC) is crucial in driving lacustrine benthic microbial processes. In lacustrine porewaters, many redox-active species exist in their reduced form, while DOC acts as a substrate and an electron acceptor. Understanding the types and abundance of redox-active species in porewaters along with their complementary DOC substrate is pivotal for gaining insights into benthic processes, particularly in regions susceptible to climate change. We report the in-situ measurement of redox-active species in sediment porewaters, alongside the ex-situ measurement of DOC extracted from cores collected from two Arctic lakes (Toolik and Fog 1). Fe2+ was abundantly detected below 4 cm of the sediment-water interface in all cores and was inversely related to dissolved O2. Additionally, two distinct Fe(III)-complexes were identified. DOC ranged in the order of 10s of mg/L and either remained stable or increased with depth. A comparison between Toolik and Fog 1 lakes revealed a higher accumulation of Fe2+ and DOC in the latter. This study marks the first of its kind to assess spatial distributions of redox-active species and DOC as a function of depth from multiple sites in Arctic lacustrine porewaters.

Mapping Dissolved Organic Carbon and Organic Iron by Comparing Deep Learning and Linear Regression Techniques Using Sentinel-2 and WorldView-2 Imagery (Byers Peninsula, Maritime Antarctica)

Byers Peninsula is considered one of the largest ice-free areas in maritime Antarctica. Since 2006, the Spanish Polar Program has taken part in a large number of environmental studies involving the effects of climate change on biological life cycles, limnology, and microbiology. Soils from maritime Antarctica are generally weakly developed and have chemical, physical, and morphological characteristics that are strongly influenced by the parent material. However, biological activity during the short Antarctic summer promotes intense transference of nutrients and organic matter in areas occupied by different species of birds and marine mammals. Mapping and monitoring those areas that are highly occupied by various species could be very useful to create models prepared from satellite images of the edaphic properties. In this approach, deep learning and linear regression models of the soil properties and spectral indexes, which were considered as explicative variables, were used. We trained the models on soil properties closely related to biological activity such as dissolved organic carbon (DOC) and the iron fraction associated with the organic matter (Fe). We tested the best approach to model the spatial distribution of DOC, Fe, and pH by training the linear regression and deep learning models on Sentinel-2 and WorldView-2 images. The most robust models, the pH model built with the deep learning approach on Sentinel images (MAE of 0.51, RMSE of 0.70, and R2 with a residual of −0.49), the DOC model built with linear regression on Sentinel images (MAE of 189.39, RMSE of 342.23, and R2 with a residual of 0.0), and the organic Fe model built with deep learning (MAE of 116.20, RMSE of 209.93, and R2 of −0.05), were used to track possible areas with ornithogenic soils, as well as areas of Byers Peninsula that could be supporting the highest biological development.

Optimizing nitrogen and phosphorus application to improve soil organic carbon and alfalfa hay yield in alfalfa fields.

Soil organic carbon (SOC) is the principal factor contributing to enhanced soil fertility and also functions as the major carbon sink within terrestrial ecosystems. Applying fertilizer is a crucial agricultural practice that enhances SOC and promotes crop yields. Nevertheless, the response of SOC, active organic carbon fraction and hay yield to nitrogen and phosphorus application is still unclear. The objective of this study was to investigate the impact of nitrogen-phosphorus interactions on SOC, active organic carbon fractions and hay yield in alfalfa fields. A two-factor randomized group design was employed in this study, with two nitrogen levels of 0 kg·ha-1 (N0) and 120 kg·ha-1 (N1) and four phosphorus levels of 0 kg·ha-1 (P0), 50 kg·ha-1 (P1), 100 kg·ha-1 (P2) and 150 kg·ha-1 (P3). The results showed that the nitrogen and phosphorus treatments increased SOC, easily oxidized organic carbon (EOC), dissolved organic carbon (DOC), particulate organic carbon (POC), microbial biomass carbon (MBC) and hay yield in alfalfa fields, and increased with the duration of fertilizer application, reaching a maximum under N1P2 or N1P3 treatments. The increases in SOC, EOC, DOC, POC, MBC content and hay yield in the 0-60 cm soil layer of the alfalfa field were 9.11%-21.85%, 1.07%-25.01%, 6.94%-22.03%, 10.36%-44.15%, 26.46%-62.61% and 5.51%-23.25% for the nitrogen and phosphorus treatments, respectively. The vertical distribution of SOC, EOC, DOC and POC contents under all nitrogen and phosphorus treatments was highest in the 0-20 cm soil layer and tended to decrease with increasing depth of the soil layer. The MBC content was highest in the 10-30 cm soil layer. DOC/SOC, MBC/SOC (excluding N0P1 treatment) and POC/SOC were all higher in the 0-40 cm soil layer of the alfalfa field compared to the N0P0 treatment, indicating that the nitrogen and phosphorus treatments effectively improved soil fertility, while EOC/SOC and DOC/SOC were both lower in the 40-60 cm soil layer than in the N0P0 treatment, indicating that the nitrogen and phosphorus treatments improved soil carbon sequestration potential. The soil layer between 0-30 cm exhibited the highest sensitivity index for MBC, whereas the soil layer between 30-60 cm had the highest sensitivity index for POC. This suggests that the indication for changes in SOC due to nitrogen and phosphorus treatment shifted from MBC to POC as the soil depth increased. Meanwhile, except the 20-30 cm layer of soil in the N0P1 treatment and the 20-50 cm layer in the N1P0 treatment, all fertilizers enhanced the soil Carbon management index (CMI) to varying degrees. Structural equation modeling shows that nitrogen and phosphorus indirectly affect SOC content by changing the content of the active organic carbon fraction, and that SOC is primarily impacted by POC and MBC. The comprehensive assessment indicated that the N1P2 treatment was the optimal fertilizer application pattern. In summary, the nitrogen and phosphorus treatments improved soil fertility in the 0-40 cm soil layer and soil carbon sequestration potential in the 40-60 cm soil layer of alfalfa fields. In agroecosystems, a recommended application rate of 120 kg·ha-1 for nitrogen and 100 kg·ha-1 for phosphorus is the most effective in increasing SOC content, soil carbon pool potential and alfalfa hay yield.

Remote Sensing Estimation of CDOM and DOC with the Environmental Implications for Lake Khanka

Chromophoric dissolved organic matter (CDOM) is a significant contributor to the biogeochemical cycle and energy dynamics within aquatic ecosystems. Hence, the implementation of a systematic and comprehensive monitoring and governance framework for the CDOM in inland waters holds significant importance. This study conducted the retrieval of CDOM in Lake Khanka. Specifically, we use the GBDT (R2 = 0.84) algorithm which performed best in retrieving CDOM levels and an empirical relationship based on the situ data between CDOM and dissolved organic carbon (DOC) to indicate the distribution of DOC indirectly. The performance of the CDOM-DOC retrieval scheme was reasonably good, achieving an R2 value of 0.69. The empirical algorithms were utilized for the analysis of Sentinel-3 datasets from the period 2016 to 2020 in Lake Khanka. The potential factors that contributed to the sources of DOM were also analyzed with the humification index (HIX). The significant relationship between CDOM and DOC (HIX and chemical oxygen demand (COD)) indicated the potential remote sensing application of water quality monitoring for water management. An analysis of our findings suggests that the water quality of the Great Khanka is superior to that of the Small Khanka. Moreover, the distribution of diverse organic matter exhibits a pattern where concentrations are generally higher along the shoreline compared to the center of the lake. Efficient measures should be promptly implemented to safeguard the water resources in international boundary lakes such as Lake Khanka and comprehensive monitoring systems including DOM distribution, DOM sources, and water quality management would be essential for water resource protection and government management.

Comparing the isotopic and molecular composition of dissolved organic carbon between the oligotrophic South China Sea and the adjacent North Pacific Ocean: Signals of biodegradation, conservative mixing, and terrestrial input

The cycling of oceanic dissolved organic carbon (DOC) is a crucial component of the global carbon cycle, yet the identification of sources and the mechanisms of its molecular transformation remain poorly understood. This study compared the isotopic and molecular composition of DOC between the oligotrophic South China Sea (SCS) and the adjacent North Pacific Ocean (NPO), and traced both its allochthonous and autochthonous sources as well as its dynamic cycling processes. DOC was collected through solid-phase extraction (SPE) from water samples of both the SCS and NPO. Carbon content, isotopic ratios, and high-resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) measurements revealed that SPE-DOC contained both labile and refractory fractions. According to our mass balance model, the labile fraction of SPE-DOC exhibited a decline from 11.5 to 12.6 μM in surface waters to a negligible concentration below 1000 m. Conversely, the refractory fraction of SPE-RDOC maintained a relatively consistent value, ranging from 12.7 to 19.0 μM across the entire water column. The vertical distribution patterns of the molecular composition and carbon isotopic ratios jointly indicated that the DOC distributions are shaped by distinct biological and physical processes within different biogeochemical realms of the water column. The production and transformation of the relatively labile DOC fractions were the dominant processes in the epipelagic and mesopelagic zones (upper 1000 m). The extent of diapycnal mixing between the SCS and NPO explained the different vertical distributions of refractory DOC molecules in the bathypelagic oceans. The molecular indices of polyphenol compounds, aromaticity, double bond saturation state, terrestrial mass peaks, and δ13C ratios of SPE-DOC indicated contributions from terrestrial sources, likely riverine input, in the SCS. This study sheds light on the molecular evidence of DOC sources, as well as their transformation and conservative mixing processes along the overturning circulation in marginal seas.

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.

Influence of the conservation mode of seawater for dissolved organic carbon analysis

Marine dissolved organic matter (DOM) is one of the largest exchangeable organic carbon reservoir on the planet. The main proxy to track the distribution of DOM in the aquatic environments remains dissolved organic carbon (DOC). Thereby the optimal protocol for long-term DOC preservation in seawater samples must be defined. In this context, we monitored bulk DOC concentrations and its size class distribution in filtered seawater samples during yearlong experiments. With different conservation mode, we tested two types of commonly used materials (borosilicate brown glass and high-density polyethylene, HDPE) and three conditioning protocols (untreated, acidified at pH 2 and frozen at −20 °C). Offshore samples collected along the entire water column of the Pacific Ocean and stored in HDPE bottles were also analysed after 2 years of storage at pH of 2 and compared to frozen samples. Results demonstrated that bulk DOC concentrations can be accurately determined in untreated samples for one month and for years in frozen samples as well as in acidified samples, when samples are stored in acid cleaned HDPE bottles or flame sealed glass ampoules. Storage in brown glass vials with Bakelite caps seems more uncertain. The study of the size class distribution of DOC reveals the possibility to study DOM for 1 month in filtered samples with no additional treatment and for years in frozen samples when stored in acid cleaned HDPE bottles. Significant changes in DOC size fractionation were observed when samples were acidified. The high molecular weight (HMW) compounds and the humic substances from the upper 1000 m were significantly degraded at pH 2, incorporating DOC in the low molecular weight (LMW) fractions. These experiments provide preservation guidelines for future studies that aim either to study bulk DOC or the chemical properties marine DOM. It is recommended to store seawater in HDPE vials at −20 °C for DOM study, or at pH 2 for bulk DOC measurements.

Response of surface soil nutrients and organic carbon fractions to tillage erosion vs. water erosion in an agricultural landscape

AbstractA mechanistic understanding of nutrient movement associated with the erosion process is required to formulate precision soil conservation measures. We explored the response of surface soil nutrients and soil organic carbon (SOC) fractions to tillage erosion and water erosion. Tillage and water erosion rates were estimated by the directional tillage erosion model and revised universal soil loss equation, respectively. One hundred and twelve surface soil samples (0–20 cm) were collected from a sloping farmland (3.6 ha) in the Mollisols region of China. Soils were analyzed for total nitrogen (TN), total phosphorus (TP), total SOC, particulate organic carbon (POC), dissolved organic carbon (DOC), and microbial biomass carbon (MBC). Results showed that no significant relation between TN and tillage or water erosion rates exists at any slope position. The TP distribution is more affected by water erosion than tillage erosion. Water erosion also played a greater role in controlling distribution of DOC than tillage erosion, whereas POC distribution was more sensitive to tillage erosion. In addition, we observed a contrasting relationship between MBC and water erosion for the mild erosion (r = −.43, P < .05) vs. intense erosion scenario (r = .38, P < .05). This shift indicates a possible dual role of microbes in SOC cycling associated with water erosion: mild erosion (averaged 17.4 t ha−1 yr−1) depletes microbial biomass and contributes to SOC mineralization, whereas intense erosion (averaged 54.6 t ha−1 yr−1) may lead to a shift in microbial structure thus promoting the dynamic replacement of SOC at eroding sites.

Distribution and microbial degradation of dissolved organic carbon in the northern South China Sea

Dissolved organic carbon (DOC) is the largest reduced carbon pool in the ocean, and it plays significant roles not only in the ocean carbon cycle but also in the control of many biogeochemical processes in the ocean. We present the concentrations and distribution of DOC in the northern South China Sea (SCS) and western North Pacific (NP) in the spring and summer seasons of 2015-2016 and 2019. Laboratory incubation bioassay experiments were also conducted to determine the microbiological respiration of DOC. In the SCS, the concentrations of DOC varied within a range of 38-95 μM, and the large spatial variations in DOC in the upper 100 m depth were influenced by a combination of factors, including primary production, terrestrial inputs from the Pearl River and the intrusion of the Kuroshio Current. The mesopelagic DOC distribution in the northern SCS basin was largely influenced by the physical mixing of upwelled deep water; however, biological processes were estimated to account for 6-20% of the modulation in DOC concentrations. Compared with the deep DOC levels in open ocean areas, a slightly excessive DOC concentration (~ 3-4 μM) was observed in the deep water of the SCS basin. Approximately 10-20% of the DOC was consumed by mesopelagic and/or deep water bacteria in the incubation bioassay experiments, and labile DOC was preferentially respired, resulting in decreased δ13C and Δ14C values of DOC.

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.

Dissolved Organic Carbon Along a Meridional Transect in the Western North Pacific Ocean: Distribution, Variation and Controlling Processes

Dissolved organic carbon (DOC) in the ocean is one of the largest reduced and exchangeable organic carbon pools on Earth and plays important roles in carbon cycling and biogeochemical processes in the ocean. Here, we report the concentrations and distributions of DOC in water samples collected along a meridional transect in the western North Pacific (NP) Ocean in November 2019. Concentrations of DOC ranged from 33-102 μM, were higher in surface water, decreased rapidly with depth to 1,000 m, and then remained relatively constant. The labile fraction of DOC accounted for 20-40% of the surface bulk DOC and was respired very rapidly in the upper 200 m depth. The semi-labile fraction of DOC accounted for 15-20% of the surface bulk DOC and was exported downward and turned over at water depths of 200-2,000 m. The formation of NP Intermediate Water (NPIW) in the Kuroshio Extension (KE) region is a major process carrying some surface semi-labile DOC down. The Low concentrations of DOC (33-44 μM) were present in the entire water column below 1,000 m along the transect in the NP. Primary production and microbial consumption played major roles in the concentration and distribution of DOC in the euphotic zone, and hydrodynamic mixing and circulation of different water masses appear to be dominant factors controlling the distribution and dynamics of DOC in the deep water of the western NP.

Distribution of particulate and dissolved organic carbon in surface waters of northern scottish fjords

Coastal waters can act concurrently as a source and sink of carbon (C), with coastal sediments trapping and storing significant quantities of C, while C is simultaneously released to the atmosphere through biogeochemical processes in the water column. The mid-to high-latitude fjords are recognised as hotspots for the burial and storage of OC in their sediments and for their potential to provide a long-term climate regulation service. Yet the distribution of particulate (POC) and dissolved organic carbon (DOC) in fjord water columns remains a significant knowledge gap, that is particularly acute in temperate vegetated systems such as those in the North Atlantic. Here we present POC and DOC data from surface waters across four Scottish fjords with differing meteorological, catchment and submarine geomorphological characteristics to both quantify and understand the factors governing the spatial distribution of POC and DOC in fjords. The measured POC and DOC concentrations in the surface waters of the four fjords are broadly analogous to other temperate vegetated fjord systems around the world. Within these systems, local factors such as submarine geomorphology is the primary factor driving POC and DOC dispersal in fjord surface waters. The data highlights that fjords are important pathways for the transport and storage of POC and DOC in the coastal ocean and that a greater focus is required on the water column OC to allow the role fjords play in near- (water column) and long-term (sediment) climate regulation to be quantified.

Distributive Features of Dissolved Organic Carbon in Aquatic Systems in the Source Area of the Yellow River on the Northeastern Qinghai–Tibet Plateau, China

Dissolved organic carbon (DOC) is the main participant in carbon cycles through water pathways. Recent studies have highlighted the roles of aquatic systems in landscape and watershed carbon budgets. This study is based on 261 samples collected between 2016 and 2017, from individual water types (e.g., river/stream, lake/pond, icing/spring, snow/rain, groundwater/ice, and others) in the source area of the Yellow River (SAYR). These samples were analyzed for examining the distributive features of DOC in aquatic systems, especially in relation to environmental factors. It shows that: 1) DOC concentrations in permafrost-related waters (7.2–234.4 mg C·L−1) were often the highest among all aquatic DOC sources (lakes/ponds: 21.3 ± 34.1 mg C·L−1, rivers/streams: 4.3 ± 3.7 mg C·L−1, and groundwater: 1.8 ± 1.4 mg C·L−1); 2) the seasonality of riverine DOC showed declining features in 2016 and high in summer/autumn, followed by a spring freshet in 2017, and a close association with intra-annual precipitation modes; 3) the main controls of aquatic DOC are permafrost presence, precipitation, and NDVI, and they contribute to 38% of variances of environmental variables in affecting variations in aquatic DOC in the SAYR; and 4) a literature review on biodegradable DOC (BDOC) of varied aquatic DOC pools indicates the highest DOC concentrations (48–1,548 mg C·L−1) and BDOC (23–71%) of ground-ice meltwater. Thus, we suggest that in the SAYR, permafrost dynamics dominate aquatic DOC distribution, and permafrost thaw may alter aquatic DOC budgets, eventually becoming an additional source for atmospheric carbon emissions.

Investigating Biochar-Derived Dissolved Organic Carbon (DOC) Components Extracted Using a Sequential Extraction Protocol

Biochar-derived dissolved organic carbon (DOC), as the most important component of biochar, can be released on farmland, improving fertility and playing a role in soil amendment and remediation. The complexity of molecular structures and diversity of DOC compounds have influenced these functions to some extent. A sequential extract protocol consisting of water (25 °C), hot water (80 °C), and NaOH solution (0.05 M) was used to fully extract DOC compounds and gain a thorough understanding of the possible DOC components released from biochar. Rape straw (RS), apple tree branches (ATB), and pine sawdust (PS) were pyrolyzed at 300, 500, and 700 °C, respectively, to make nine distinct biochars. A TOC analyser, ultraviolet-visible spectroscopy (UV–vis), and excitation–emission fluorescence (EEM) spectrophotometer were used in conjunction with parallel factor analysis (PARAFAC) to determine the distribution of DOC content, the diversity of aromaticity, molecular weight characteristics and components of biochar-derived DOC. The results show that the relative distribution of water-extractable fractions ranged from 3.21 to 35.57%, with a low-aromaticity and extremely hydrophilic fulvic-acid-like compounds being found in the highest amounts (C2 and C3). The smallest amount of hot water-extractable components was produced from the release of small-molecule aliphatic compounds adsorbed on biochar and susceptible to migration loss once in a soil solution. More than half of the biochar-derived DOC was released in a NaOH solution, which primarily consisted of humic-acid-like compounds (C1), with higher molecular weights, more aromaticity, and lower bioavailability, according to the distribution of DOC in various extractants. In addition, the pyrolysis temperature and biomass type had a significant impact on the DOC properties released by biochar. As a result, the findings of this study showed that using a sequential extract protocol of water, hot water, and NaOH solution in combination with spectroscopic methods could successfully reveal the diversity of biochar-derived components, which could lead to new insights for the accurate assessment of potential environmental impacts and new directions for biochar applications.

Factors Controlling the Spatial Distribution of Dissolved Organic Matter With Changes in the C/N Ratio From the Upper to Lower Reaches of the Ishikari River, Japan

Dissolved organic matter (DOM), particularly dissolved organic nitrogen (DON), is an important source of energy and/or organic nutrients for heterotrophic microorganisms in rivers. Although various factors controlling the quantity and quality of stream and riverine DOM have been extensively studied, DON has been under-researched compared to dissolved organic carbon (DOC). The spatial distribution of DOC and DON concentrations with respect to the C/N ratio and DOM optical properties was investigated in the Ishikari River and its tributaries in Hokkaido, northern Japan. Here, the upper reaches are forested and the middle and lower reaches are encompassed by agricultural land, in particular paddy fields. Furthermore, dark incubation experiments were conducted using filtered riverine water (<0.7 µm) to determine the bioavailability of DOC and DON (particularly due to small microorganisms) considered as a factor controlling the spatial distribution. In the mainstream, DOC and DON concentrations increased with river flow in the upper and middle reaches and remained unchanged in the lower reaches. The C/N ratio of bulk DOM decreased continuously from the upper reaches to lower reaches. The optical properties exhibited changes in the DOM characteristics in terms of higher molecular weight and higher aromaticity from the upper to middle reaches, suggesting that flooded paddy fields largely altered the riverine DOM concentration and composition. In the lower reaches, the C/N ratio of the bulk DOM decreased with the river flow. However, according to principal component analysis, no changes were observed in the optical properties with river flow, suggesting that the C/N ratio of bulk DOM changed owing to in situ biological activity in the river. DOC biodegradation was observed at four sites in the upper and middle reaches but not at the two sites in the lower reaches. However, the DON concentration during the dark incubation experiments at all sites did not differ significantly, which implies that microbial degradation, particularly by small microorganisms, is a factor that decreased the C/N ratio of bulk DOM in the upper and middle reaches. In contrast, large microorganisms possibly degraded C-rich DOM to decrease the C/N ratio of bulk DOM in the lower reaches of the Ishikari River.

Distribution and influencing factors of soil organic carbon in a typical karst catchment undergoing natural restoration

Understanding the distribution patterns and controlling factors of soil organic carbon (SOC) in karst areas is important for soil carbon management. However, due to the wide variety of human activities and karst habitats, the factors influencing SOC in karst areas vary. A typical catchment undergoing natural restoration in the karst region of South China was investigated to determine the distribution and variation of soil properties and SOC stocks (SOCSs) under three types of terrain: a hillslope, a depression and a sinkhole. The factors influencing SOC under the different terrain types were determined by redundancy analysis and multiple linear regression modelling. The results indicated that terrain and hydrological conditions affect the distribution of SOC on the hillslope. The spatial heterogeneity of SOC and dissolved organic carbon (DOC) on the hillslope was high. Terrain type and land use differences significantly affected the SOC and DOC concentrations at the catchment scale. SOC loss was more serious in the depression due to agricultural activities, and SOC accumulation was more obvious on the hillslope due to its relatively long natural restoration period. The average SOCSs of the hillslope were 16.5% and 54.6% larger than those of the depression and sinkhole, respectively, and the average dissolved organic carbon stocks (DOCSs) were 70.6% and 179.7% larger, respectively. In addition, the impacts of environmental factors on SOC and DOC varied among the different terrain types. Soil texture and topography were the main factors controlling the distribution of SOC and DOC on the hillslope and in the whole catchment, and soil texture was the main factor controlling SOC at the catchment scale. In addition, soil loss through sinkholes may be an important carbon sink in karst areas. The results of this study are of great significance for evaluating soil carbon storage and vegetation restoration strategies in karst areas.

Aerobic respiration in riparian exchange zones of regulated river corridors

AbstractRiver stage fluctuations drive surface water‐groundwater exchanges within river corridors. This study evaluates how repeated daily stage fluctuations, representative of hydropeaking conditions, influence aerobic respiration of river‐sourced dissolved organic carbon (DOC) in the riparian exchange zone using reactive flow and transport simulations. Over 50 hypothetical scenarios were modelled to evaluate how the duration of the daily flood signal, river DOC concentration, aquifer hydraulic conductivity and ambient groundwater flow condition affect the fate and transport of DOC and DO in the riparian aquifer. Time series subsurface snapshots highlight how the various factors influence the subsurface distribution of DOC and DO. The total mass of DOC respired per meter of river had a wide range depending on the parameters, spanning from 1.4 to 71 g over 24‐h, with high hydraulic conductivity and losing ambient groundwater flow conditions favouring the largest amount of DOC respired. The ratio of DOC mass entering the riparian zone with the mass returning to the river showed that as little as 5% to as much as 76% of the DOC that enters the bank during stage fluctuations returns to the river. This return ratio is dependent on river DOC concentration, hydraulic conductivity and ambient groundwater flow. The results illustrate that stage variations due to river regulation can be a significant control on aerobic respiration in riparian exchange zones.

Evidence of Deep DOC Enrichment via Particle Export Beneath Subarctic and Northern Subtropical Fronts in the North Pacific

Here we provide compelling evidence that deep particle export enhanced dissolved organic carbon (DOC) concentrations beneath the Pacific’s Subarctic Front (SA, ∼42°N) and Northern Subtropical Front (NST, ∼34°N). We report three main findings: First, deep export of subjectively small particles (128–512 μm) was apparent throughout the frontal zone in which the SA resides. However, export of large particles was specifically associated with the SA, rather than the entire frontal zone, and appeared to exclusively transfer DOC into the bathypelagic water column. Second, a similar DOC enrichment existed beneath the NST, though this signal was curiously not accompanied by observable particles (>128 μm). We conclude that export occurring previously in winter left this DOC behind as a residue, though the associated particles were no longer present by spring. Third, the presence of strong hydrographic fronts was not the only control on export that resulted in these unique DOC distributions. Deep export and DOC enrichment was also controlled by latitude-specific biogeochemical and hydrographic conditions, such as depth of the nutricline and seasonal mixed layer shoaling. Given these observations, the fronts within the transitional region of the North Pacific are clearly special locations for deep carbon sequestration and for providing uncommon DOC enrichment that ultimately supports the deep microbial community.