Dissolved Organic Carbon Production Research Articles

Karst carbon sink mechanism and its contribution to carbon neutralization under land- use management

The chemical weathering process of carbonate rocks consumes a large quantity of CO2. This has great potential as a carbon sink, and it is one of a significant pathway for achieving carbon neutrality. However, the control mechanisms of karst carbon sink fluxes are unclear, and there is a lack of effective and accurate accounting. We took the Puding Shawan karst water‑carbon cycle test site in China, which has identical initial conditions but different land use types, as the research subject. We used controlled experiments over six years to evaluate the mechanisms for the differences in hydrology, water chemistry, concentrations and fluxes of dissolved organic carbon (DOC) and dissolved inorganic carbon (DIC). We found that the transition from rock to bare soil to grassland led to increases in the DIC concentration by 0.08–0.62 mmol⋅L−1. The inorganic carbon sink flux (CSF) increased by 3.01–5.26 t⋅C⋅km−2⋅a−1, an increase amplitude of 30–70 %. The flux of dissolved organic carbon (FDOC) increase by 0.28 to 0.52 t⋅C⋅km−2⋅a−1, an increase amplitude of 34–90 %. We also assessed the contribution of land use modifications to regional carbon neutrality, it indicate that positive land use modification can significantly regulate the karst carbon sink, with grassland having the greatest carbon sequestration ability. Moreover, in addition to DOC from soil organic matter degradation, DOC production by chemoautotrophic microorganisms utilizing DIC in groundwater may also be a potential source. Thus, coupled studies of the conversion of DIC to DOC processes in groundwater are an important step in assessing karst carbon sink fluxes.

Arsenic-Hyperaccumulator Pteris vittata Effectively Uses Sparingly-Soluble Phosphate Rock: Rhizosphere Solubilization, Nutrient Improvement, and Arsenic Accumulation.

Sparingly-soluble phosphate rock (PR), a raw material for P-fertilizer production, can be effectively utilized by the As-hyperaccumulator Pteris vittata but not most plants. In this study, we investigated the associated mechanisms by measuring dissolved organic carbon (DOC) and acid phosphatase in the rhizosphere, and nutrient uptake and gene expression related to the As metabolism in P. vittata. The plants were grown in a soil containing 200 mg kg-1 As and/or 1.5% PR for 30 days. Compared to the As treatment, the P. vittata biomass was increased by 33% to 4.6 g plant-1 in the As+PR treatment, corresponding to 27% decrease in its frond oxidative stress as measured by malondialdehyde. Due to PR-enhanced DOC production in the rhizosphere, the Ca, P, and As contents in P. vittata fronds were increased by 17% to 9.7 g kg-1, 29% to 5.0 g kg-1, and 57% to 1045 mg kg-1 in the As+PR treatment, thereby supporting its better growth. Besides, PR-induced rhizosphere pH increase from 5.0 to 6.9 promoted greater P uptake by P. vittata probably via upregulating low-affinity P transporters PvPTB1;1/1;2 by 3.7-4.1 folds. Consequently, 29% lower available-P induced the 3.3-fold upregulation of high-affinity P transporter PvPht1;3 in the As+PR treatment, which was probably responsible for the 58% decrease in available-As content in the rhizosphere. Consistent with the enhanced As translocation and sequestration, arsenite antiporters PvACR3/3;3 were upregulated by 1.8-4.4 folds in the As+PR than As treatment. In short, sparingly-soluble PR enhanced the Ca, P, and As availability in P. vittata rhizosphere and improved their uptake via upregulating genes related to As metabolism, suggesting its potential application for improving phytoremediation in As-contaminated soils.

Synoptic sampling reveals spatial stability in flow and chemistry patterns despite large seasonal variability in a subarctic mountain catchment

AbstractSeasonality plays a critical role in cold mountain regions as variation in air temperature, ground thermal status, and precipitation phase alter the rate, timing and magnitude of hydrological and chemical transport. Additionally, cold mountain catchments can have highly variable topography, geology, permafrost, and landcover, which intrinsically add to this irregularity. Understanding how external and internal variability act to control mass fluxes requires sampling at a high spatial resolution over time, which rarely occurs in cold remote regions. In this work, we conduct five snapshot sampling surveys across 34 subcatchments during the ice‐free period in Wolf Creek Research Basin (a mesoscale montane subarctic catchment) and two additional winter surveys across a subset of sites to assess the drivers of variability in stream chemistry and discharge. We sampled for specific conductance (SpC), major ions, and dissolved organic carbon (DOC) and used statistical metrics and Bayesian mixing analysis to quantify patterns of flow and chemistry across space and time. Our results indicate patterns in both flow and chemistry remain largely consistent across seasons for all solutes. However, there was weaker correlation of chemistry between sites, suggesting asynchronous behaviour within the catchment. There was evidence of increasing production of ions and DOC along the stream network during high spring flows but not during low flows. Although concentrations and flows exhibit high seasonality in subarctic mountains, this seasonal variability does not alter spatial patterns that arise from highly variable catchment characteristics.

Internal carbon recycling by heterotrophic prokaryotes compensates for mismatches between phytoplankton production and heterotrophic consumption.

Molecular observational tools are useful for characterizing the composition and genetic endowment of microbial communities but cannot measure fluxes, which are critical for the understanding of ecosystems. To overcome these limitations, we used a mechanistic inference approach to estimate dissolved organic carbon (DOC) production and consumption by phytoplankton operational taxonomic units and heterotrophic prokaryotic amplicon sequence variants and inferred carbon fluxes between members of this microbial community from Western English Channel time-series data. Our analyses focused on phytoplankton spring and summer blooms, as well as bacteria summer blooms. In spring blooms, phytoplankton DOC production exceeds heterotrophic prokaryotic consumption, but in bacterial summer blooms heterotrophic prokaryotes consume three times more DOC than produced by the phytoplankton. This mismatch is compensated by heterotrophic prokaryotic DOC release by death, presumably from viral lysis. In both types of summer blooms, large amounts of the DOC liberated by heterotrophic prokaryotes are reused through internal recycling, with fluxes between different heterotrophic prokaryotes being at the same level as those between phytoplankton and heterotrophic prokaryotes. In context, internal recycling accounts for approximately 75% and 30% of the estimated net primary production (0.16 vs 0.22 and 0.08 vs 0.29μmoll-1 d-1) in bacteria and phytoplankton summer blooms, respectively, and thus represents a major component of the Western English Channel carbon cycle. We have concluded that internal recycling compensates for mismatches between phytoplankton DOC production and heterotrophic prokaryotic consumption, and we encourage future analyses on aquatic carbon cycles to investigate fluxes between heterotrophic prokaryotes, specifically internal recycling.

Soil Organic Carbon Lateral Movement Processes Integrated Into a Terrestrial Ecosystem Model

AbstractLateral movement of soil organic carbon (SOC) induced by soil erosion and runoff changes spatial distributions of SOC, and further changes the land‐atmosphere CO2 exchange and terrestrial carbon budget. However, current ecosystem models do not or only poorly integrate the process of SOC lateral movement and cannot simulate the impacts of soil erosion on the carbon cycle. This study integrated SOC erosion and deposition processes into a process‐based ecosystem model (i.e., Integrated BIosphere Simulator (IBIS)), and separately simulated the lateral movements of dissolved organic carbon (DOC) and particulate organic carbon (POC). The model was evaluated in three river basins in Northeast China that are dominated by cropland, forest, and grassland. The results showed that the model reproduced well the production, erosion, and deposition of DOC and POC. The annual SOC lateral movement (1.34–7.22 g C m−2 yr−1) induced by erosion in the three tested basins was 0.27%–1.45% of the annual net primary production. The model developed in this study has great implications for simulating the lateral movements of SOC in terrestrial ecosystems, which can improve model performance in projecting the terrestrial carbon budget.

Suboxic DOM is bioavailable to surface prokaryotes in a simulated overturn of an oxygen minimum zone, Devil's Hole, Bermuda.

Oxygen minimum zones (OMZs) are expanding due to increased sea surface temperatures, subsequent increased oxygen demand through respiration, reduced oxygen solubility, and thermal stratification driven in part by anthropogenic climate change. Devil's Hole, Bermuda is a model ecosystem to study OMZ microbial biogeochemistry because the formation and subsequent overturn of the suboxic zone occur annually. During thermally driven stratification, suboxic conditions develop, with organic matter and nutrients accumulating at depth. In this study, the bioavailability of the accumulated dissolved organic carbon (DOC) and the microbial community response to reoxygenation of suboxic waters was assessed using a simulated overturn experiment. The surface inoculated prokaryotic community responded to the deep (formerly suboxic) 0.2 μm filtrate with cell densities increasing 2.5-fold over 6 days while removing 5 μmol L-1 of DOC. After 12 days, the surface community began to shift, and DOC quality became less diagenetically altered along with an increase in SAR202, a Chloroflexi that can degrade recalcitrant dissolved organic matter (DOM). Labile DOC production after 12 days coincided with an increase of Nitrosopumilales, a chemoautotrophic ammonia oxidizing archaea (AOA) that converts ammonia to nitrite based on the ammonia monooxygenase (amoA) gene copy number and nutrient data. In comparison, the inoculation of the deep anaerobic prokaryotic community into surface 0.2 μm filtrate demonstrated a die-off of 25.5% of the initial inoculum community followed by a 1.5-fold increase in cell densities over 6 days. Within 2 days, the prokaryotic community shifted from a Chlorobiales dominated assemblage to a surface-like heterotrophic community devoid of Chlorobiales. The DOM quality changed to less diagenetically altered material and coincided with an increase in the ribulose-1,5-bisphosphate carboxylase/oxygenase form I (cbbL) gene number followed by an influx of labile DOM. Upon reoxygenation, the deep DOM that accumulated under suboxic conditions is bioavailable to surface prokaryotes that utilize the accumulated DOC initially before switching to a community that can both produce labile DOM via chemoautotrophy and degrade the more recalcitrant DOM.

Effects of ocean acidification on growth and photophysiology of two tropical reef macroalgae.

Macroalgae can modify coral reef community structure and ecosystem function through a variety of mechanisms, including mediation of biogeochemistry through photosynthesis and the associated production of dissolved organic carbon (DOC). Ocean acidification has the potential to fuel macroalgal growth and photosynthesis and alter DOC production, but responses across taxa and regions are widely varied and difficult to predict. Focusing on algal taxa from two different functional groups on Caribbean coral reefs, we exposed fleshy (Dictyota spp.) and calcifying (Halimeda tuna) macroalgae to ambient and low seawater pH for 25 days in an outdoor experimental system in the Florida Keys. We quantified algal growth, calcification, photophysiology, and DOC production across pH treatments. We observed no significant differences in the growth or photophysiology of either species between treatments, except for lower chlorophyll b concentrations in Dictyota spp. in response to low pH. We were unable to quantify changes in DOC production. The tolerance of Dictyota and Halimeda to near-future seawater carbonate chemistry and stability of photophysiology, suggests that acidification alone is unlikely to change biogeochemical processes associated with algal photosynthesis in these species. Additional research is needed to fully understand how taxa from these functional groups sourced from a wide range of environmental conditions regulate photosynthesis (via carbon uptake strategies) and how this impacts their DOC production. Understanding these species-specific responses to future acidification will allow us to more accurately model and predict the indirect impacts of macroalgae on coral health and reef ecosystem processes.

Seasonal and Storm Event‐Based Dynamics of Dissolved Organic Carbon (DOC) Concentration in a Mediterranean Headwater Catchment

AbstractThis study investigates the spatial and temporal dynamics of Dissolved Organic carbon (DOC) concentration in a Mediterranean headwater catchment (Turbolo River catchment, southern Italy) equipped with two multi‐parameter sondes providing more than two‐year (May 2019–November 2021) continuous high‐frequency measurements of several DOC‐related parameters. The sondes were installed in two nested sections, a quasi‐pristine upstream sub‐catchment and a downstream outlet with anthropogenic water quality disturbances. DOC estimates were achieved by correcting the fluorescent dissolved organic matter—fDOM—values through an original procedure not requiring extensive laboratory measurements. Then, DOC dynamics at the seasonal and storm event scales were analyzed. At the seasonal scale, results confirmed the climate control on DOC production, with increasing background concentrations in hot and dry summer months. The hydrological regulation proved crucial for DOC mobilization and export, with the top 10th percentile of discharge associated with up to 79% of the total DOC yield. The analysis at the storm scale using flushing and hysteresis indices highlighted substantial differences between the two catchments. In the steeper upstream catchment, the limited capability of preserving hydraulic connection over time with DOC sources determined the prevalence of transport as the limiting factor to DOC export. In the downstream catchment, transport‐ and source‐limited processes were observed almost equally. The correlation between the hysteretic behavior and antecedent precipitation was not linear since the process reverted to transport‐limited for high accumulated rainfall values. Exploiting high‐resolution measurements, the study provided insights into DOC export dynamics in nested headwater catchments at multiple time scales.

Spatially distributed tracer‐aided modelling to explore DOC dynamics, hot spots and hot moments in a tropical mountain catchment

AbstractTracer‐aided rainfall‐runoff modelling is a promising tool for understanding catchment hydrology, particularly when tracers provide information about coupled hydrological‐biogeochemical processes. Such models allow for predicting the quality and quantity of water under changing climatic and anthropogenic conditions. Here, we present the Spatially‐distributed Tracer‐Aided Rainfall‐Runoff model with a coupled biogeochemical reactive tracer module (STARR‐DOC) to simulate dissolved organic carbon (DOC) dynamics and sources. The STARR‐DOC model was developed and tested for a humid high Andean ecosystem (páramo) using high‐resolution hourly DOC and hydrometeorological data to simulate hourly discharge and DOC at a fine spatial (10 × 10 m) resolution. Overall, the model was able to acceptably reproduce discharge (KGE ~ 0.45) and stream DOC (KGE ~ 0.69) dynamics. Spatially distributed DOC simulations were independently compared using point DOC measurements for different soil types across the catchment, which allowed for identifying DOC production hot spots and hot moments. Results showed higher hydrological connectivity between slopes and valleys with increasing precipitation. Wetter conditions also favoured DOC production (wet month = 82 mg L−1, dry month = 5 mg L−1) and transport to the stream network (DOC concentrations: during events ~15 mg L−1, during baseflows ~4 mg L−1). Our results also suggest that minor changes in meteorological conditions directly affect páramo soil water dynamics and biogeochemistry. Knowledge of when and where DOC production in mountain catchments is greatest is important for water managers to understand when they make decisions about water security, especially considering climate change predictions for the Andean region.

Dynamics of the Marine Dissolved Organic Carbon Reservoir in Glacial Climate Simulations: The Importance of Biological Production

AbstractThe marine dissolved organic carbon (DOC) reservoir rivals the atmospheric carbon inventory in size. Recent work has suggested that the size of the DOC reservoir may respond to variations in sea temperature and global overturning circulation strength. Moreover, mobilization of marine DOC has been implicated in paleoclimate events including Cryogenian glaciation and Eocene hyperthermals. Despite these suggestions, the dynamics of the marine DOC reservoir are poorly understood, and previous carbon cycle modeling has generally assumed this reservoir to be static. In this study, we utilize an Earth system model of intermediate complexity to assess the response of the marine DOC reservoir to various glacial boundary conditions. Our results indicate that the marine DOC reservoir is responsive to glacial perturbations and may shrink or expand on the order of 10–100 Pg C. In contrast to recent studies that emphasize the importance of DOC degradation in driving the mobility of DOC reservoir, our study indicates the importance of DOC production. In the experiment under full glacial boundary conditions, for example, a 19% drop in net primary production leads to an 81 Pg C reduction in the DOC pool, without which the atmospheric CO2 concentration would have been lower by approximately 38 ppm by dissolved inorganic carbon changes alone. Thus, DOC reservoir variability is necessary to fully account for the simulated changes in atmospheric CO2 concentration. Our findings based on glacial experiments are corroborated in a different set of simulations using freshwater flux to induce weakening of the Atlantic meridional overturning circulation.

Marine nutrient subsidies promote biogeochemical hotspots in undisturbed, highly humic estuaries

AbstractThe land‐ocean dissolved organic carbon (DOC) flux represents a significant term within the global carbon budget, with peatland‐dominated regions representing the most intense sources of terrestrial DOC export. As the interface between freshwater and marine systems, estuaries have the potential to act as a filter of the land‐ocean carbon flux, removing terrestrially derived DOC, which is present at low concentrations in the oceans, via a combination of physicochemical and biological processes. However, the fate of peat‐derived DOC within estuaries remains poorly quantified, partly due to the complicating influences of heterogeneous soils, land‐use, point sources, and upstream modification of organic matter. To minimize these modifying factors, we studied DOC and inorganic nutrients in four small, peat‐dominated, minimally disturbed, and oligotrophic Falkland Island estuaries. Contrary to expectations, we found limited evidence of physicochemical estuarine DOC removal, and instead observed apparent “hot zones” of biogeochemical activity, where terrestrially‐derived silicate mixed with inorganic nitrogen and phosphorus entering the estuaries from the nutrient‐rich marine ecosystem. In two estuaries, this coincided with apparent in situ DOC production. We suggest that the observed phenomena of marine nutrient subsidy of estuarine productivity, and flexible utilization of multiple nutrients within the oligotrophic system, may once have been widespread in temperate estuaries. However, this function has been lost in many ecosystems due to catchment eutrophication by agricultural and urban development. We conclude that the estuaries of the Falkland Islands provide a valuable pre‐disturbance analogue for natural biogeochemical functioning in temperate estuaries receiving high organic matter inputs.

Biogenic carbon pool production maintains the Southern Ocean carbon sink

Through biological activity, marine dissolved inorganic carbon(DIC) is transformed into different types of biogenic carbon available for export to the ocean interior, including particulate organic carbon (POC), dissolved organic carbon (DOC), and particulate inorganic carbon (PIC). Each biogenic carbon pool has a different export efficiency that impacts the vertical ocean carbon gradient and drives natural air-sea carbon dioxide gas (CO2) exchange. In the Southern Ocean (SO), which presently accounts for ~40% of the anthropogenic ocean carbon sink, it is unclear how the production of each biogenic carbon pool contributes to the contemporary air-sea CO2 exchange. Based on 107 independent observations of the seasonal cycle from 63 biogeochemical profiling floats, we provide the basin-scale estimate of distinct biogenic carbon pool production. We find significant meridional variability with enhanced POC production in the subantarctic and polar Antarctic sectorsand enhanced DOC production in the subtropical and sea-ice-dominated sectors. PIC production peaks between 47°S and 57°S near the "great calcite belt." Relative to an abiotic SO, organic carbon production enhances CO2 uptake by 2.80 ± 0.28 Pg C y-1, while PIC production diminishes CO2 uptake by 0.27 ± 0.21 Pg C y-1. Without organic carbon production, the SO would be a CO2 source to the atmosphere. Our findings emphasize the importance of DOC and PIC production, in addition to the well-recognized role of POC production, in shaping the influence of carbon export on air-sea CO2 exchange.

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.

No effect of ocean acidification on growth, photosynthesis, or dissolved organic carbon release by three temperate seaweeds with different dissolved inorganic carbon uptake strategies

AbstractIn a future ocean, dissolved organic carbon (DOC) release by seaweed has been considered a pathway for organic carbon that is not incorporated into growth under carbon dioxide (CO2) enrichment/ocean acidification (OA). To understand the influence of OA on seaweed DOC release, a 21-day experiment compared the physiological responses of three seaweed species, two which operate CO2 concentrating mechanisms (CCMs), Ecklonia radiata (C. Agardh) J. Agardh and Lenormandia marginata (Hooker F. and Harvey) and one that only uses CO2 (non-CCM), Plocamium cirrhosum (Turner) M.J. Wynne. These two groups (CCM and non-CCM) are predicted to respond differently to OA dependent on their affinities for Ci (defined as CO2 + bicarbonate, HCO3−). Future ocean CO2 treatment did not drive changes to seaweed physiology—growth, Ci uptake, DOC production, photosynthesis, respiration, pigments, % tissue carbon, nitrogen, and C:N ratios—for any species, regardless of Ci uptake method. Our results further showed that Ci uptake method did not influence DOC release rates under OA. Our results show no benefit of elevated CO2 concentrations on the physiologies of the three species under OA and suggest that in a future ocean, photosynthetic CO2 fixation rates of these seaweeds will not increase with Ci concentration.

Mobilization of subsurface carbon pools driven by permafrost thaw and reactivation of groundwater flow: a virtual experiment

Permafrost thaw leads to an increase in groundwater circulation and potential mobilization of organic carbon sequestered in deep Arctic sediments (e.g. 3–25 m below surface). Upon thaw, a portion of this carbon may be transported along new groundwater flow paths to surface waters or be microbially transformed or immobilized by in-situ biogeochemical reactions. The fate of thaw-mobilized carbon impacts surface water productivity and global climate. We developed a numerical model to investigate the effects of subsurface warming, permafrost thaw, and resultant increased groundwater flow on the mobilization and reactive transport of dissolved organic carbon (DOC). Synthetic simulations demonstrate that mobilization and groundwater-borne DOC export are determined by subsurface thermo-chemical conditions that control the interplay of DOC production (organic matter degradation), mineralization, and sorption. Results suggest that peak carbon mobilization from these depths precedes complete permafrost loss, occurring within two centuries of thaw initiation with the development of supra-permafrost groundwater flow systems. Additionally, this study highlights the lack of field data needed to constrain these new models and apply them in real-word site-specific applications, specifically the amount and spatial variability of organic carbon in deep sediments and data to constrain DOC production rates for groundwater systems in degrading permafrost. Modeling results point to key biogeochemical parameters related to organic matter and carbon bioavailability to be measured in the field to bridge the gap between models and observations. This study provides a foundation for further developing a physics-based modeling framework to incorporate the influence of groundwater flow and permafrost thaw on permafrost DOC dynamics and export, which is imperative for advancing understanding and prediction of carbon release and terrestrial-aquatic carbon exchange in warming Artic landscapes in the coming decades.

Photochemical and microbial transformation of particulate organic matter depending on its source and size

Particulate organic matter (POM) in water systems can be converted into dissolved organic matter (DOM) through various pathways depending on its properties and transformation. Thus, information on the behavior of POM is crucial for fully understanding water systems and the carbon cycle. In this study, the effects of particle size and the source of POM, as well as photochemical and microbial changes in DOM characteristics subsequently released from POM were evaluated using various spectral indices, excitation-emission matrix combined with parallel factor analysis components, and principal component analysis. The amount of dissolved organic carbon (DOC) released from POM during suspension was significantly associated with the carbon content of POM (p < 0.05). The amount of DOC (mg-C/g-SS) decreased in mineral-bound POM as a result of microbial degradation but increased in biogenic POM as a result of microbial dissolution, owing to the structural differences in organic matter from different sources. Mineral-bound POM showed more DOC production by photochemical desorption than microbial degradation, whereas biogenic POM displayed the opposite trend. The DOM derived from fine POM had more humified terrestrial humic-like substances than those derived from coarse POM. Principal components 1 and 2 were associated with DOC production and degree of humification, respectively. The increase in the degree of aromaticity and humification of organic matter was higher in mineral-bound POM by photochemical desorption of highly humified organic matter and in the biogenic POM by microbial dissolution. In conclusion, this study was able to provide basic information on the transformation of POM, thus, it is expected to broaden the knowledge of the biogeochemical cycle of organic matter.

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 &amp;lt;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.

Evaluation of the factors governing dissolved organic carbon concentration in the soil solution of a temperate forest organic soil

The widespread increase of dissolved organic carbon (DOC) in northern hemisphere surface waters have been generally attributed to the recovery from acidic deposition and to climatic variations. The long-term responses of DOC to environmental drivers could be better predicted with a better understanding of the mechanisms taking place at the soil level given organic forest soils are the main site of DOC production in forested watersheds. Here, we assess the long-term variation (25 years) of DOC concentration in the solution leaching from the soil organic layer (DOCOL) of a temperate forest. Our results show that DOCOL increased by 32 % (p < 0.001) during the period of study while the lake outlet DOC concentration did not show any changes. Weekly and annual models based on a simple set of explicative variables including throughfall DOC, throughfall precipitation, temperature, litterfall amounts and organic layer leachate calcium concentration (CaOL, taken as a proxy for soil solution ionic strength) explain between 17 and 58 % of the variance in DOCOL depending on model structures and temporal scales. Throughfall DOC and CaOL were both positively related to DOCOL in the models describing its variations at the weekly and annual scale. Temperature was positively correlated to DOCOL, probably due to increased microbial activity, while precipitation had a negative effect on DOCOL (only at the weekly scale), most probably due to a dilution effect. Contrary to our expectations, annual litterfall inputs had no impacts on annual DOCOL variations. Overall, the results shows that DOCOL control is a complex process implicating a set of environmental factors that are acting in different ways while no single variable alone can explain a large part of the variation in both, weekly or annual DOCOL variations.

Spatiotemporal patterns and drivers of terrestrial dissolved organic carbon (DOC) leaching into the European river network

Abstract. Leaching of dissolved organic carbon (DOC) from soils into the river network is an important component of the land carbon (C) budget. At regional to global scales, its significance has been estimated through simple mass budgets, often using multi-year averages of observed fluvial DOC fluxes as a proxy of DOC leaching due to the limited availability of observations of the leaching flux itself. This procedure leads to a systematic underestimation of the leaching flux because of the decay of DOC during fluvial transport. Moreover, this procedure does not allow for revealing spatiotemporal variability in DOC leaching from soils, which is vital to better understand the drivers of DOC leaching and its impact on the local soil C budget. In this study, we use the land surface model (LSM) ORCHILEAK to simulate the terrestrial C budget, including leaching of DOC from the soil and its subsequent reactive transport through the river network of Europe. The model performance is evaluated not only against the sparse observations of the soil DOC leaching rate, but also against the more abundant observations of fluxes and reactivity of DOC in rivers, providing further evidence that our simulated DOC fluxes are realistic. The model is then used to simulate the spatiotemporal patterns of DOC leaching across Europe over the period 1972–2012, quantifying both the environmental drivers of these patterns and the impact of DOC leaching on the land C budget. Over the simulation period, we find that, on average, 14.3 Tg C yr−1 of DOC is leached from land into European rivers, which is about 0.6 % of the terrestrial net primary production (NPP), a fraction significantly lower than that reported for tropical river networks. On average, 12.3 Tg C yr−1 of the leached DOC is finally exported to the coast via the river network, and the rest is respired during transit. DOC leaching presents a large seasonal variability, with the maximum occurring in winter and the minimum in summer, except for most parts of northern Europe, where the maximum occurs in spring due to snowmelt. The DOC leaching rate is generally low in warm and dry regions, and high in the cold and wet regions of Europe. Furthermore, runoff and the ratio between runoff from shallower flow paths on one hand and deep drainage and groundwater flow on the other hand are the main drivers of the spatiotemporal variation of DOC leaching. Temperature, as a major control of DOC production and decomposition rates in the soils, plays only a secondary role.

Partitioning the Export of Distinct Biogenic Carbon Pools in the Northeast Pacific Ocean Using a Biogeochemical Profiling Float

AbstractWe leverage observations from chemical and bio‐optical sensors mounted on a biogeochemical profiling float in the Northeast Pacific Ocean to quantify the cycling and export potential of distinct biogenic carbon pools, including particulate inorganic carbon (PIC), particulate organic carbon (POC), and dissolved organic carbon (DOC). Year‐round observations reveal complex carbon cycle dynamics among these carbon pools. Net DOC production peaked during bloom initiation, about 3 months prior to the summer peak in POC production. We validate the float estimates of DOC cycling with seasonal accumulation and removal rates derived from ship‐board DOC observations over the same period. By combining chemical and bio‐optical tracers of POC cycling, we estimate the instantaneous POC sinking flux (). The cooccurrence of DOC consumption and POC production and sinking during fall and winter resolves the regional conundrum of a persistent particle sinking flux observed by sediment traps during a season that is known to be heterotrophic. PIC production is small, and uncertainties are large. By combining float‐based estimates of instantaneous net primary production (NPP) and , we quantify a real‐time carbon export ratio ([/NPP] × 100%) for the euphotic zone. Elevated export ratios during summer are associated with an increase in the fraction of particles larger than 100 μm in size. Elevated export ratios during winter are associated with the physical redistribution of particles through seasonal deep mixing. Our study demonstrates how the combined use of multiple sensors on biogeochemical profiling floats can provide more nuanced information about upper ocean carbon cycle dynamics.