Dissolved Black Carbon Concentrations Research Articles

Top-down control over dissolved organic carbon in the bottom water of the Weddell Sea and its implication for the continental shelf pump

Dense water out of the Antarctic shelves is expected to drive the transport of carbon into the deep Southern Ocean via the formation of Antarctic Bottom Water. However, bottom water formation’s capacity to sequester carbon into the deep ocean is poorly constrained. Here, dissolved organic carbon (DOC), dissolved black carbon (DBC), and particulate organic carbon (POC) were examined to reveal the influence of the Weddell Sea Deep Water (WSDW) on DOC transport during its flowing out of the Weddell Sea. High DOC concentrations (>60 μM-C) and low DBC/DOC ratios (<1.5%) were observed in surface water near the South Orkney Islands, ascribing to sea ice melt-induced phytoplankton blooms. Seawater at the mid-deep depths exhibited a higher DOC concentration (averaging 48.1 ± 3.7 μM-C) than the incoming water source, resulting from the release of DOC from sinking particles. Bottom water had higher DOC concentration compared to the mid-deep layer water (t-test, p < 0.005), while the DBC concentrations were comparable. In addition, the excess DOC (relative to WSDW) in bottom water showed a close relation with POC in surface water. These results reveal a top-down control over the DOC concentration in bottom water through a quick sinking of diatom detritus and subsequently solubilization in bottom water and/or sediment. With an estimate, the WSDW carries 5.1 ± 2.8 Tg-C/yr of excess DOC out of the Powell Basin, representing an important carbon source to the deep Southern Ocean. This study highlights the key role of the Antarctic continental shelf pump in carbon sequestration.

Measuring dissolved black carbon in water via aqueous, inorganic, high-performance liquid chromatography of benzenepolycarboxylic acid (BPCA) molecular markers.

Dissolved black carbon (DBC) is the condensed aromatic portion of dissolved organic matter produced from the incomplete combustion of biomass and other thermogenic processes. DBC quantification facilitates the examination of the production, accumulation, cycling, transformation, and effects of biologically recalcitrant condensed aromatic carbon in aquatic environments. Due to the heterogeneous nature of DBC molecules, concentrations are difficult to measure directly. Here, the method for DBC quantification consists of oxidizing condensed aromatic carbon to benzenepolycarboxylic acids (BPCAs), which are used as proxies for the assessment of DBC in the original sample. The concentrations of oxidation products (BPCAs) are quantified using high-performance liquid chromatography. DBC concentrations are determined from the concentration of BPCAs using a previously established conversion factor. Details and full descriptions of the preparative and analytical procedures and techniques of the BPCA method are usually omitted for brevity in published method sections and method-specific papers. With this step-by-step protocol, we aim to clarify the steps of DBC analysis, especially for those adopting or conducting the BPCA method for the first time.

Occurrence of dissolved black carbon in source water and disinfection byproducts formation during chlorination

Dissolved black carbon (DBC), the water-soluble component of black carbon, which is formed by incomplete combustion of fossil fuels or biochar, takes up about 10% of dissolved organic matter (DOM) in river water. However, the distribution of DBC in water environment especially in source water is not clear and as an important component of DOM, whether DBC can produce disinfection byproducts (DBPs) like other DOM during disinfection remains unknown. In this study, the DBC concentrations in seventeen source water samples from East China were measured. The concentrations of DBC in the source water samples ranged from 60 to 270 μg/L, which were positively correlated with UV254 absorbance and chemical oxygen demand. The levels of DBC in wet season were higher than that in dry season. The average concentrations of DBC in different types of source water samples followed the order of reservoir > canal > lake > river. DBC could only be removed by 20% during the simulated coagulation, and further generate different categories of DBPs during chlorination, among which the concentrations of haloacetic acids (HAA) were the highest. The results indicated that DBC widely distributes in source water and is an important precursor of HAAs and THMs during chlorination.

Fate of dissolved black carbon in the deep Pacific Ocean

Black carbon (BC), a byproduct of biomass and fossil fuel combustion, may impact the climate because it can be stored on Earth’s surface for centuries to millennia. Dissolved BC (DBC) occurs ubiquitously in the ocean. However, the DBC cycle in the ocean has not been well constrained. Here, we show the basin-scale distribution of DBC in the Pacific Ocean and find that the DBC concentrations in the deep Pacific Ocean decrease along with deep-ocean meridional circulation. The DBC concentration is negatively correlated with apparent oxygen utilization, a proxy of the integrated flux of sinking particles, in the deep Pacific Ocean, implying that DBC is removed from the deep ocean to abyssal sediments through sorption onto sinking particles. The burial flux of BC to abyssal sediments is estimated to be 0.040–0.085 PgC yr−1, corresponding to 1.5–3.3% of the anthropogenic CO2 uptake by the ocean.

Dissolved Black Carbon and Semivolatile Aromatic Hydrocarbons in the Ocean: Two Entangled Biogeochemical Cycles?

Dissolved black carbon (DBC) plays a role in the oceanic carbon cycle. DBC originates from the heating and incomplete combustion of organic matter, including fossil fuels, a shared origin with polycyclic aromatic hydrocarbons (PAH). DBC is quantified using the benzene polycarboxylic acids produced by oxidation of the organic extract, a fraction of which derive from PAHs and other semivolatile aromatic-like compounds (SALCs). However, the current view of the DBC cycle does not take into account the inputs and sinks known for PAHs, such as diffusive air–water exchange and degradation. A meta-analysis of oceanic PAHs, SALCs, and DBC concentrations shows that SALCs account for 16% of DBC (ranging from 5% to 31%). Such a large contribution of semivolatile aromatic hydrocarbons to DBC is consistent with the large atmospheric input of SALCs (estimated as 400 Tg C y–1). Furthermore, photodegradation at the surface ocean and microbial degradation in the water column of semivolatile DBC can be important sinks, consistent with the ubiquitous occurrence of the degradation genes of the metabolic routes for aromatic hydrocarbons. Future work should focus on the characterization of semivolatile DBC and its degradation in order to constrain its contribution to refractory organic matter and the anthropogenic perturbation of the carbon cycle.

Investigating Atmospheric Inputs of Dissolved Black Carbon to the Santa Barbara Channel During the Thomas Fire (California, USA)

AbstractThe Thomas Fire ignited on December 4, 2017 and burned for over one month. As the Thomas Fire burned, Santa Ana winds carried a thick plume of smoke and ash over the Santa Barbara Channel. We sought to determine whether the deposition of Thomas Fire ash to the Santa Barbara Channel had a measurable effect on the concentration and stable carbon isotopic composition (δ13C) of dissolved black carbon (DBC) in coastal waters. DBC is the condensed aromatic fraction of thermally altered organic carbon quantified using the benzenepolycarboxylic acid (BPCA) method. DBC δ13C signatures were determined via BPCA‐specific stable carbon isotopic analysis. Surface water DBC concentrations beneath the smoke plume were up to 13% higher than other sampling stations. Via controlled leaching experiments, we found that Thomas Fire ash released a considerable amount of DBC in seawater (1.4 g‐DBC per kg of ash organic carbon), which was further enhanced by photodissolution. By combining in situ and experimental data, we constructed an isotopic mixing model to estimate inputs of ash‐derived DBC to marine surface waters. Although we were able to detect slight elevations in DBC concentrations beneath the smoke plume, the ash‐derived contributions were too small to meaningfully shift the δ13C signature, which resulted in an observed mismatch between modeled and measured DBC δ13C values. Few studies have investigated the immediate impacts of wildfire on coastal biogeochemistry. Therefore, our work provides an important foundation for understanding atmospheric contributions of fire‐derived DBC to coastal margins.

Spatial characteristics and removal of dissolved black carbon in the western Arctic Ocean and Bering Sea

In the Arctic, large amounts of black carbon (BC) are released into river water and transported to the oceans as dissolved BC (DBC). However, the cycling and fate of DBC in the ocean is poorly understood. Here, DBC, dissolved organic carbon (DOC), absorbance, and δ18O were analyzed to examine the spatial characteristics and removal of DBC in the western Arctic Ocean and the Bering Sea during the boreal summer. DBC concentrations ranged from 0.67 to 4.18 μmol-C L−1. In the sea-ice free regions, high DBC and DOC concentrations and a254 values corresponded to high δ18O-derived meteoric water contents, indicating that river discharge dominated their spatial patterns. By contrast, sea-ice meltwater (SIM) appeared to dilute DBC and DOC in SIM impacted waters (SIM > 3.5%). The departure of DBC from conservative mixing lines suggested that 47–84% of riverine DBC was removed over the shelves with 7–23% transported to the upper Canada Basin. These results suggest that shelf regions are crucial sites for riverine DBC removal that modulate the delivery of DBC to the open Arctic Ocean.

Transport of dissolved black carbon from marginal sea sediments to the western North Pacific

Pyrogenic carbon, also called black carbon (BC), is produced by biomass burning as well as by fossil fuel combustion and is an important slow-cycling component in the global carbon cycle. BC occurs in a fraction of marine dissolved organic carbon, and this is called dissolved BC (DBC). Marine DBC has been considered the ultimate repository for fluvial DBC; however, the environmental dynamics of marine DBC have not been well documented. In this study, vertical DBC profiles from the surface to the deep layers of the western subarctic Pacific and its marginal seas were analyzed using the benzenepolycarboxylic acid (BPCA) method. DBC concentrations tended to be highest in the surface layer and decreased with increasing depth, except for those in the Bussol’ Strait locatedin the Kuril Islands between the Sea of Okhotsk and the North Pacific. Vertical distributions of the condensation degree index of DBC (i.e., the ratio of B5CA and B6CA to all BPCAs) did not show a general trend with depth. Atmospheric deposition of BC is likely a major source of DBC in the surface layer. In the intermediate layer, the DBC concentration and the condensation degree index in the Bussol’ Strait were higher than those in the western subarctic Pacific. The occurrence of highly condensed DBC observed in the Bussol’ Strait was accompanied by low salinity and a high DO concentration, indicating that DBC is transported from the shelf sediments of the Sea of Okhotsk to the Bussol’ Strait by dense shelf water (DSW) and Okhotsk Sea Intermediate Water (OSIW). The DBC concentration and the condensation degree index in the intermediate layer of the Bering Sea and the Kamchatka Strait (locatedin the Aleutian Islands between the Bering Sea and the North Pacific) were higher than those in the western subarctic Pacific but lower than those in the Bussol’ Strait; this suggests that DBC from the slope sediments in the Bering Sea is transported to the Kamchatka Strait by the East Kamchatka Current and that the DBC flux from the slope sediments of the Bering Sea is lower than that involving the DSW in the Sea of Okhotsk, which accompanies the resuspension of shelf sediments. The results of this study imply that sedimentary BC is an important source of water column DBC in marginal seas and the adjacent open ocean.

Dissolved black carbon enhanced the aquatic photo-transformation of chlortetracycline via triplet excited-state species: The role of chemical composition

Dissolved black carbon (DBC), widely distributed in the aquatic environments, can accelerate sunlight-driven photo-transformation of micropollutants, however the photosensitization mechanisms are not clear. Herein, the DBC was extracted from bamboo biochar and fractionated by molecular weight (i.e. <10 k, <3 k, and <1 k Da). The effects of DBC on chlortetracycline (CTC) photolysis behaviors, and the role of chemical composition (i.e., molecular weight and chemical structure) in DBC-mediated photo-transformation were investigated. The results showed that DBC could accelerate CTC photodegradation significantly. At low DBC concentrations (<6.0 mg C/L), the photodegradation rate constant of CTC increased from 0.0299 to 0.0416 min−1 with the increasing DBC concentration. Via quenching experiment, the triplet excited-state of DBC was identified as the dominant reactive intermediate with >90% contribution to total CTC photodegradation. In addition, it was found that the photosensitive efficiency of DBC increased as the molecular weight decreased, and the stronger photosensitization ability exhibited in DBC with low-molecular weight was potentially attributed to its higher content of carbonyl compounds. The observed photosensitive efficiency of DBC sharply decreased after reduction by NaBH4, further confirming the key role of carbonyl compounds in the photosensitization process. Moreover, based on the result of photoproducts, the amidogen in CTC was verified to be susceptible to react with 3DBC*.

Environmental Controls on the Riverine Export of Dissolved Black Carbon

AbstractEach year, tropical rivers export a dissolved organic carbon (DOC) flux to the global oceans that is equivalent to ~4% of the global land sink for atmospheric CO2. Among the most refractory fractions of terrigenous DOC is dissolved black carbon (DBC), which constitutes ~10% of the total DOC flux and derives from the charcoal and soot (aerosol) produced during biomass burning and fossil fuel combustion. Black carbon (BC) has disproportionate storage potential in oceanic pools and so its export has implications for the fate and residence time of terrigenous organic carbon (OC). In contrast to bulk DOC, there is limited knowledge of the environmental factors that control riverine fluxes of DBC. We thus completed a comprehensive assessment of the factors controlling DBC export in tropical rivers with catchments distributed across environmental gradients of hydrology, topography, climate, and soil properties. Generalized linear models explained 70 and 64% of the observed variance in DOC and DBC concentrations, respectively. DOC and DBC concentrations displayed coupled responses to the dominant factors controlling their riverine export (soil moisture, catchment slope, and catchment stocks of OC or BC, respectively) but varied divergently across gradients of temperature and soil properties. DBC concentrations also varied strongly with aerosol BC deposition rate, indicating further potential for deviation of DBC fluxes from those of DOC due to secondary inputs of DBC from this unmatched source. Overall, this study identifies the specific drivers of BC dynamics in river catchments and fundamentally enhances our understanding of refractory DOC export to the global oceans.

Hydrological Controls on the Seasonal Variability of Dissolved and Particulate Black Carbon in the Altamaha River, GA

AbstractRivers play an important role in the transport of organic carbon from terrestrial to marine environments. A significant portion of this material is black carbon (BC), a residue of incomplete biomass and fossil fuel combustion. BC is mobilized in fluvial systems as both particulate BC (PBC) and dissolved BC (DBC), and the export of BC to coastal environments may have significant implications for carbon cycling in marine environments. However, while little is known regarding the potential connectivity between riverine export of PBC and DBC or the potential importance of such a relationship in constraining future BC budgets, current knowledge suggests that fluvial export of PBC and DBC are decoupled in small fire‐impacted watersheds. This study aims to further address this subject on a larger watershed scale. For this study, 13 monthly samples were collected (September 2015 to September 2016) near the mouth of the Altamaha River, Georgia. PBC and DBC were characterized using the benzenze polycarboxylic acid method. Seasonal hydrology and regional shifts in storm events play an important role for both PBC and DBC export during high flow months. The DBC concentrations were comparable among wet and dry seasons, whereas evidence of seasonal salt water intrusions suggests an additional estuarine contribution of PBC at the sampling location. The DBC and PBC fluxes were generally coupled, although this pattern was disrupted during initial storm pulses. While this is the first report of potential coupling between DBC and PBC export, environmental drivers controlling this behavior between DBC and PBC remain to be constrained.

Dissolved black carbon in aquatic ecosystems

AbstractThe incomplete combustion of organic molecules produces a chemically diverse suite of pyrogenic residues termed black carbon (BC). The significance of BC cycling on land has long been recognized, and the recognition of dissolved BC (DBC) as a major component of the aquatic carbon cycle is developing rapidly. As we seek a greater understanding of DBC cycling, our interpretation of environmental DBC concentrations and molecular composition should take into account both the formation conditions of charred residues, and the physico‐chemical transformation of DBC that occurs during transit within aquatic systems. We present the current state of knowledge concerning sources, processing, and sinks of DBC in inland, coastal/estuarine, and ocean waters. We feature studies and new methodologies which focus specifically on the aquatic cycling of DBC, explore the relationship between particulate and dissolved BC, and highlight research gaps which should be targeted to advance our current knowledge of DBC biogeochemistry.

Do Regional Aerosols Contribute to the Riverine Export of Dissolved Black Carbon?

AbstractThe fate of black carbon (BC), a stable form of thermally altered organic carbon produced during biomass and fuel combustion, remains an area of uncertainty in the global carbon cycle. The transfer of photosynthetically derived BC into extremely long‐term oceanic storage is of particular significance and rivers are the key linkage between terrestrial sources and oceanic stores. Significant fluvial fluxes of dissolved BC to oceans result from the slow release of BC from degrading charcoal stocks; however, these fluvial fluxes may also include undetermined contributions of aerosol BC, produced by biomass and fossil fuel combustion, which are deposited in river catchments following atmospheric transport. By investigation of the Paraíba do Sul River catchment in Southeast Brazil we show that aerosol deposits can be substantial contributors to fluvial fluxes of BC. We derived spatial distributions of BC stocks within the catchment associated with soil charcoal and with aerosol from both open biomass burning and fuel combustion. We then modeled the fluvial concentrations of dissolved BC (DBC) in scenarios with varying rates of export from each stock. We analyzed the ability of each scenario to reproduce the variability in DBC concentrations measured in four data sets of river water samples collected between 2010 and 2014 and found that the best performing scenarios included a 5–18% (135–486 Mg DBC year−1) aerosol contribution. Our results suggest that aerosol deposits of BC in river catchments have a shorter residence time in catchments than charcoal BC and, therefore, contribute disproportionately (with respect to stock magnitude) toward fluvial fluxes of BC.

Dissolved black carbon in the global cryosphere: Concentrations and chemical signatures

AbstractBlack carbon (BC) is derived from the incomplete combustion of biomass and fossil fuels and can enhance glacial recession when deposited on snow and ice surfaces. Here we explore the influence of environmental conditions and the proximity to anthropogenic sources on the concentration and composition of dissolved black carbon (DBC), as measured by benzenepolycaroxylic acid (BPCA) markers, across snow, lakes, and streams from the global cryosphere. Data are presented from Antarctica, the Arctic, and high alpine regions of the Himalayas, Rockies, Andes, and Alps. DBC concentrations spanned from 0.62 μg/L to 170 μg/L. The median and (2.5, 97.5) quantiles in the pristine samples were 1.8 μg/L (0.62, 12), and nonpristine samples were 21 μg/L (1.6, 170). DBC is susceptible to photodegradation when exposed to solar radiation. This process leads to a less condensed BPCA signature. In general, DBC across the data set was composed of less polycondensed DBC. However, DBC from the Greenland Ice Sheet (GRIS) had a highly condensed BPCA molecular signature. This could be due to recent deposition of BC from Canadian wildfires. Variation in DBC appears to be driven by a combination of photochemical processing and the source combustion conditions under which the DBC was formed. Overall, DBC was found to persist across the global cryosphere in both pristine and nonpristine snow and surface waters. The high concentration of DBC measured in supraglacial melt on the GRIS suggests that DBC can be mobilized across ice surfaces. This is significant because these processes may jointly exacerbate surface albedo reduction in the cryosphere.

Seasonal dynamics of atmospheric and river inputs of black carbon, and impacts on biogeochemical cycles in Halong Bay, Vietnam

Emissions of black carbon (BC), a product of incomplete combustion of fossil fuels, biofuels and biomass, are high in the Asia-Pacific region, yet input pathways and rates to the ocean are not well constrained. Atmospheric and riverine inputs of BC in Halong Bay (Vietnam), a hotspot of atmospheric BC, were studied at monthly intervals during one year. Climate in Halong Bay is governed by the monsoon regime, characterized by a northeast winter monsoon (dry season) and southeast summer monsoon (wet season). During the dry season, atmospheric BC concentrations averaged twice those observed during the wet season. In the sea surface microlayer (SML) and underlying water (ULW), concentrations of particulate BC (PBC) averaged 539 and 11 µmol C L–1, respectively. Dissolved BC (DBC) concentrations averaged 2.6 µmol C L–1 in both the SML and ULW. Seasonal variations indicated that PBC concentration in the SML was controlled by atmospheric deposition during the dry season, while riverine inputs controlled both PBC and DBC concentrations in ULW during the wet season. Spatiotemporal variations of PBC and DBC during the wet season suggest that river runoff was efficient in transporting PBC that had accumulated on land during the dry season, and in mobilizing and transporting DBC to the ocean. The annual river flux of PBC was about 3.8 times higher than that of DBC. The monsoon regime controls BC input to Halong Bay by favoring dry deposition of BC originating from the north during the dry season, and wet deposition and river runoff during the wet season. High PBC concentrations seem to enhance the transfer of organic carbon from dissolved to particulate phase by adsorbing dissolved organic carbon and stimulating aggregation. Such processes may impact the availability and biogeochemical cycling of other dissolved substances, including nutrients, for the coastal marine ecosystem.

Spatial Distributions and Seasonal Variations of Dissolved Black Carbon in the Bohai Sea, China

ABSTRACT Huang, G. P.; Chen, Y. J.; Tian, C. G.; Tang, J. H.; Zhang, H.; Luo, Y. M.; Li, J., and Zhang, G., 2016. Spatial distributions and seasonal variations of dissolved black carbon in the Bohai Sea, China. To investigate the temporal and spatial variations of dissolved black carbon (DBC) concentrations in the Bohai Sea, China, 495 seawater samples on 141 sites were collected in different water depths and seasons in six cruises from 2010 to 2014 for DBC quantification by the molecular marker method-benzene polycarboxylic acid method. The average concentration of DBC was 96.6 ± 32.9μg L−1(n = 495)in the entire Bohai Sea,while it was 136.2 ± 33.7 μg L−1(n = 28) in the Laizhou Bay, 131.2 ± 30.3 μg L−1(n = 44) in the Bohai Bay, 86.3± 16.1μg L−1(n = 66) in the Liaodong Bay, 89.6±19.8μg L−1(n = 277) in the Central Bohai Basin and 57.8 ± 8.6 μg L−1(n = 80) in the Bohai Strait respectively. DBC concentrations showed a distinct decreasing trend from coastal area to offshore area and from the internal Bohai Sea...

Utilizing colored dissolved organic matter to derive dissolved black carbon export by arctic rivers

Wildfires have produced black carbon (BC) since land plants emerged. Condensed aromatic compounds, a form of BC, have accumulated to become a major component of the soil carbon pool. Condensed aromatics leach from soils into rivers, where they are termed dissolved black carbon (DBC). The transport of DBC by rivers to the sea is a major term in the global carbon and BC cycles. To estimate Arctic river DBC export, 25 samples collected from the six largest Arctic rivers (Kolyma, Lena, Mackenzie, Ob’, Yenisey and Yukon) were analyzed for dissolved organic carbon (DOC), colored dissolved organic matter (CDOM), and DBC. A simple, linear regression between DOC and DBC indicated that DBC accounted for 8.9 ± 0.3% DOC exported by Arctic rivers. To improve upon this estimate, an optical proxy for DBC was developed based upon the linear correlation between DBC concentrations and CDOM light absorption coefficients at 254 nm (a254). Relatively easy to measure a254 values were determined for 410 Arctic river samples between 2004 and 2010. Each of these a254 values was converted to a DBC concentration based upon the linear correlation, providing an extended record of DBC concentration. The extended DBC record was coupled with daily discharge data from the six rivers to estimate riverine DBC loads using the LOADEST modeling program. The six rivers studied cover 53% of the pan-Arctic watershed and exported 1.5 ± 0.1 million tons of DBC per year. Scaling up to the full area of the pan-Arctic watershed, we estimate that Arctic rivers carry 2.8 ± 0.3 million tons of DBC from land to the Arctic Ocean each year. This equates to ~8% of Arctic river DOC export, slightly less than indicated by the simpler DBC vs DOC correlation-based estimate. Riverine discharge is predicted to increase in a warmer Arctic. DBC export was positively correlated with river runoff, suggesting that the export of soil BC to the Arctic Ocean is likely to increase as the Arctic warms.

Dissolved black carbon in boreal forest and glacial rivers of central Alaska: assessment of biomass burning versus anthropogenic sources

Boreal forests are thought to be an important source and sink for pyrogenic carbon, or black carbon (BC), as fire is very common in this type of ecosystem. However, the reported soil BC content in boreal forests is low, suggesting active removal processes of soil BC possibly through transfer to the dissolved phase. In this study, dissolved black carbon (DBC) concentrations from samples collected from streams in Alaska boreal forest watersheds and in glacial rivers are reported. The DBC levels, as well as its degree of polycondensation, in glacial rivers are much lower than those from boreal forest streams. This suggests source differences (fossil fuel vs. forest fires) as a possible reason for these molecular variations. Our hypothesis is that DBC in boreal forest watersheds is mostly generated from forest fires, while glacial rivers will receive a higher relative contribution of BC from atmospheric deposition, resulting in a more fossil fuel like molecular signature of DBC in the latter. To test the source hypothesis, we compared the DBC molecular characteristics of samples from boreal rives and glacier-fed streams with additional samples from locations isolated from significant fire-derived inputs, where atmospheric deposition of anthropogenic soot may be important. Based on this comparative approach, we suggest that anthropogenic BC, associated with small soot particles, is the most prominent source of DBC in the glacial rivers. A linear positive correlation between dissolved organic carbon (DOC) and DBC concentrations was observed for both boreal forest and glacial samples, once again confirming that DOC and DBC dynamics are closely coupled. The ever increasing export of DOC associated DBC from high latitude boreal forests and glaciers as a result of global warming, may impact DOC quality and ultimately trophic dynamics in the receiving marine environment.

Biogeochemistry of dissolved organic matter in an anoxic intertidal creek bank

Seawater circulation in permeable coastal sediments is driven by tidal changes in hydraulic gradients. The resulting submarine groundwater discharge is a source of nutrients and dissolved organic matter (DOM) to the water column. Yet, little is known about the cycling of DOM within tidal sediments, because the molecular DOM characterization remains analytically challenging. One technique that can dissect the multitude of molecules in DOM is ultrahigh-resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS). To aim at a high resolution DOM analysis we study the seasonal turnover and marine and terrestrial sources of DOM in an intertidal creek bank of the southern North Sea down to 3m depth and link the biogeochemical processes to FT-ICR-MS data and the analyses of inorganic porewater chemistry, δ13C of solid-phase extracted dissolved organic carbon (SPE-DOC), dissolved black carbon (DBC) and dissolved carbohydrates (DCHO). Increasing concentrations of dissolved Fe, Mn, P, total alkalinity, dissolved nitrogen, DOC and a concomitant decrease of sulfate along the seawater circulation path from the upper tidal flat to the tidal flat margin indicate continuous microbial activity. The relative increase of Si concentrations, unsaturated aliphatics, peptide molecular formulae and isotopically more 13C-enriched SPE-DOC towards the tidal flat margin suggests that remineralization processes mobilize DOM from buried algal (diatoms) and microbial biomass. Porewater in sediments <100cm depth contains 13C-depleted SPE-DOC and highly unsaturated compounds which are probably derived from eroded peats, suggesting rapid removal of bioavailable marine DOM such as DCHO from the water column and selective enrichment of terrestrial DOM. DBC concentrations are highest in the discharging porewater close to the tidal creek suggesting that the intertidal flat is an important DBC source to the coastal ocean. Porewater DOM accumulating at the low water line is enriched in N and S. We hypothesize that this is partly due to DOM reacting with dissolved sulfide and ammonium which may increase the refractory character of the DOM, hence making it less bioavailable for in situ active microbes.

Dissolved black carbon in grassland streams: Is there an effect of recent fire history?

While the existence of black carbon as part of dissolved organic matter (DOM) has been confirmed, quantitative determinations of dissolved black carbon (DBC) in freshwater ecosystem and information on factors controlling its concentration are scarce. In this study, stream surface water samples from a series of watersheds subject to different burn frequencies in Konza Prairie (Kansas, USA) were collected in order to determine if recent fire history has a noticeable effect on DBC concentration. The DBC levels detected ranged from 0.04 to 0.11mgL−1, accounting for ca. 3.32±0.51% of dissolved organic carbon (DOC). No correlation was found between DBC concentration and neither fire frequency nor time since last burn. We suggest that limited DBC flux is related to high burning efficiency, possibly greater export during periods of high discharge and/or the continuous export of DBC over long time scales. A linear correlation between DOC and DBC concentrations was observed, suggesting the export mechanisms determining DOC and DBC concentrations are likely coupled. The potential influence of fire history was less than the influence of other factors controlling the DOC and DBC dynamics in this ecosystem. Assuming similar conditions and processes apply in grasslands elsewhere, extrapolation to a global scale would suggest a global grasslands flux of DBC on the order of 0.14Mtcarbonyear−1.