The concentrations and carbon isotopic (C-13, C-14) compositions of total organic carbon (TOC) and black carbon (BC) were measured for four sediment cores collected from the shelf to slope in the Arctic Ocean. Contents of TOC and BC ranged from 0.46% to 1.94% and 0.04% to 0.13% by dry weight, and BC accounted for 3.5% to 15.2% of the TOC preserved in the shelf and slope sediments. Sediment of the Chukchi shelf contained relatively high BC contents compared with the sediments of the Arctic slope, suggesting strong influence from the river and terrestrial inputs to the shelf region. Radiocarbon measurements revealed that the ages of BC are in the range of 7330 to 29,700 years (before present) and they are 4093 to 7723 years older than the C-14 ages of TOC preserved in the same sediment depths. Based on an isotopic mass balance model, we calculated that fossil fuel combustion contributed 62-96%, and biomass burning contributed 4-38% of the BC pool in the sediments of the study area. This "slow-cycling" old BC is an important fraction of the inert organic carbon pool preserved in the sediments, and represents a significant sink of atmospheric CO2 and global carbon cycle. With the thawing permafrost caused by continuous global warming, the size of this BC pool mobilized and exported by rivers to the Arctic Ocean could increase in the future. (C) 2019 Elsevier B.V.

Global biomass burning generates 40 million to 250 million tons of charcoal every year, part of which is preserved for millennia in soils and sediments. We have quantified dissolution products of charcoal in a wide range of rivers worldwide and show that globally, a major portion of the annual charcoal production is lost from soils via dissolution and subsequent transport to the ocean. The global flux of soluble charcoal accounts to 26.5 ± 1.8 million tons per year, which is ~10% of the global riverine flux of dissolved organic carbon (DOC). We suggest that the mobilization of charcoal and DOC out of soils is mechanistically coupled. This study closes a major gap in the global charcoal budget and provides critical information in the context of geoengineering.

Black carbon (BC) is a recalcitrant form of organic carbon (OC) produced by landscape fires. BC is an important component of the global carbon cycle because, compared to unburned biogenic OC, it is selectively conserved in terrestrial and oceanic pools. Here we show that the dissolved BC (DBC) content of dissolved OC (DOC) is twice greater in major (sub)tropical and high-latitude rivers than in major temperate rivers, with further significant differences between biomes. We estimate that rivers export 18 ± 4 Tg DBC year globally and that, including particulate BC fluxes, total riverine export amounts to 43 ± 15 Tg BC year (12 ± 5% of the OC flux). While rivers export ~1% of the OC sequestered by terrestrial vegetation, our estimates suggest that 34 ± 26% of the BC produced by landscape fires has an oceanic fate. Biogeochemical models require modification to account for the unique dynamics of BC and to predict the response of recalcitrant OC export to changing environmental conditions.

Black carbon (BC) enters the ocean through aerosol and river deposition. BC makes up 12 to 31 percent of the sedimentary organic carbon (SOC) at two deep ocean sites, and it is 2400 to 13,900 carbon-14 years older than non-BC SOC deposited concurrently. BC is likely older because it is stored in an intermediate reservoir before sedimentary deposition. Possible intermediate pools are oceanic dissolved organic carbon (DOC) and terrestrial soils. If DOC is the intermediate reservoir, then BC is 4 to 22 percent of the DOC pool. If soils are the intermediate reservoir, then the importance of riverine carbon in the ocean carbon cycle has been underestimated.

The production of pyrogenic carbon (PyC; a continuum of organic carbon (C) ranging from partially charred biomass and charcoal to soot) is a widely acknowledged C sink, with the latest estimates indicating that ~50% of the PyC produced by vegetation fires potentially sequesters C over centuries. Nevertheless, the quantitative importance of PyC in the global C balance remains contentious, and therefore, PyC is rarely considered in global C cycle and climate studies. Here we examine the robustness of existing evidence and identify the main research gaps in the production, fluxes and fate of PyC from vegetation fires. Much of the previous work on PyC production has focused on selected components of total PyC generated in vegetation fires, likely leading to underestimates. We suggest that global PyC production could be in the range of 116-385 Tg C yr(-1), that is ~0.2-0.6% of the annual terrestrial net primary production. According to our estimations, atmospheric emissions of soot/black C might be a smaller fraction of total PyC (<2%) than previously reported. Research on the fate of PyC in the environment has mainly focused on its degradation pathways, and its accumulation and resilience either in situ (surface soils) or in ultimate sinks (marine sediments). Off-site transport, transformation and PyC storage in intermediate pools are often overlooked, which could explain the fate of a substantial fraction of the PyC mobilized annually. We propose new research directions addressing gaps in the global PyC cycle to fully understand the importance of the products of burning in global C cycle dynamics.© 2015 The Authors. Global Change Biology Published by John Wiley & Sons Ltd.

This review highlights the ubiquity of black carbon (BC) produced by incomplete combustion of plant material and fossil fuels in peats, soils, and lacustrine and marine sediments. We examine various definitions and analytical approaches and seek to provide a common language. BC represents a continuum from partly charred material to graphite and soot particles, with no general agreement on clear‐cut boundaries. Formation of BC can occur in two fundamentally different ways. Volatiles recondense to highly graphitized soot‐BC, whereas the solid residues form char‐BC. Both forms of BC are relatively inert and are distributed globally by water and wind via fluvial and atmospheric transport. We summarize, chronologically, the ubiquity of BC in soils and sediments since Devonian times, differentiating between BC from vegetation fires and from fossil fuel combustion. BC has important implications for various biological, geochemical and environmental processes. As examples, BC may represent a significant sink in the global carbon cycle, affect the Earth's radiative heat balance, be a useful tracer for Earth's fire history, build up a significant fraction of carbon buried in soils and sediments, and carry organic pollutants. On land, BC seems to be abundant in dark‐colored soils, affected by frequent vegetation burning and fossil fuel combustion, thus probably contributing to the highly stable aromatic components of soil organic matter. We discuss challenges for future research. Despite the great importance of BC, only limited progress has been made in calibrating analytical techniques. Progress in the quantification of BC is likely to come from systematic intercomparison using BCs from different sources and in different natural matrices. BC identification could benefit from isotopic and spectroscopic techniques applied at the bulk and molecular levels. The key to estimating BC stocks in soils and sediments is an understanding of the processes involved in BC degradation on a molecular level. A promising approach would be the combination of short‐term laboratory experiments and long‐term field trials.

Black carbon (BC), produced by incomplete combustion of fossil fuels and vegetation, occurs ubiquitously in soils and sediments. BC exists as a continuum from partly charred material to highly graphitized soot particles, with no general agreement on clear‐cut boundaries of definition or analysis. In a comparative analysis, we measured BC forms in eight soil samples by six established methods. All methods involved removal of the non‐BC components from the sample by thermal or chemical means or a combination of both. The remaining carbon, operationally defined as BC, was quantified via mass balance, elemental composition or by exploiting benzenecarboxylic acids as molecular markers or applying 13C MAS NMR (magic angle spinning nuclear magnetic resonance) spectroscopy. BC concentrations measured for individual samples vary over 2 orders of magnitude (up to a factor of 571). One possible explanation for this wide range of results is that the individual BC methods rely on operational definitions with clear‐cut but different boundaries and developed for specific scientific questions, whereas BC represents a continuum of materials with widely contrasting physicochemical properties. Thus the methods are inherently designed to analytically determine different parts of the continuum, and it is crucial to know how measurements made by different techniques relate to each other. It is clear from this preliminary comparative analysis that a collection of BC reference materials should be established as soon as possible 1) to ensure long‐term intralaboratory and interlaboratory data quality and 2) to facilitate comparative analyses between different analytical techniques and scientific approaches

The chemo-thermal oxidation method at 375°C (CTO-375) has been widely used to quantify black carbon (BC) in sediments. In the present study, CTO-375 was tested and adapted for application to soil, accounting for some matrix specific properties like high organic carbon (≤ 39%) and carbonate (≤ 37%) content. Average recoveries of standard reference material SRM-2975 ranged from 25 to 86% for nine representative Swiss and Indian samples, which is similar to literature data for sediments. The adapted method was applied to selected samples of the Swiss soil monitoring network (NABO). BC content exhibited different patterns in three soil profiles while contribution of BC to TOC was found maximum below the topsoil at all three sites, however at different depths (60-130 cm). Six different NABO sites exhibited largely constant BC concentrations over the last 25 years, with short-term (6 months) prevailing over long-term (5 years) temporal fluctuations.Copyright © 2010 Elsevier Ltd. All rights reserved.

Many optical, thermal and chemical methods exist for the measurement of elemental carbon (EC) but are unable or neglect to differentiate between the different forms of EC such as char- or soot-EC. The thermal/optical reflectance (TOR) method applies different temperatures for measuring EC and organic carbon (OC) contents through programmed, progressive heating in a controlled atmosphere, making available eight separate carbon fractions - four OC, one pyrolyzed organic carbon, and three EC. These fractions were defined by temperature protocol, oxidation atmosphere, and laser-light reflectance/transmittance. Stepwise thermal evolutional oxidation of the TOR method makes it possible to distinguish char- from soot-EC. In this study, different EC reference materials, including char and soot, were used for testing it. The thermograms of EC reference materials showed that activation energy is lower for char- than soot-EC. Low-temperature EC1 (550 degrees C in a 98% He/2% O2 atmosphere) is more abundant for char samples. Diesel and n-hexane soot samples exhibit similar EC2 (700 degrees C in a 98% He/2% O2 atmosphere) peaks, while carbon black samples peaks at both EC2 and EC3 (800 degrees C in a 98% He/2% O2 atmosphere). These results supported the use of the TOR method to discriminate between char- and soot-EC.

Three techniques were used to measure black carbon (BC) in samples from Chinese loess-paleosol sequences. The results obtained by (1) chemo-thermal oxidation (CTO, performed two ways), (2) acid dichromate oxidation (Cr2O7), and (3) thermal-optical reflectance (TOR) were intercompared because prior studies have shown that the methods can yield disparate results. BC concentrations did vary among the methods, most likely because they measured different components of the BC continuum, but the high-temperature BC (soot) determined by CTO was correlated with the BC and soot obtained by TOR. The CTO and TOR methods both yielded statistically significant linear relationships for loess and lake sediments that had incremental additions of a standard (SRM-1649a). The results also showed that charred material was more abundant in these test sediments than soot carbon. Data for BC in Luochuan loess generated using TOR showed a trend similar to that of magnetic susceptibility, that is, high BC and large susceptibilities during the last interglacial and low values for both variables in the last glacial. The results thus indicate that the TOR method is well suited for studies of sedimentary materials and that more biomass burned during the last interglacial than in the last glacial.Copyright © 2012 Elsevier Ltd. All rights reserved.

Levels of total organic carbon (TOC) and black carbon (BC) were determined together with those of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in the selected eighteen coastal sites (n = 285) along the Arabian Sea from Pakistan. Results showed that the total concentration of TOC, BC, ∑OCPs and ∑26PCBs ranged between 0.3 and 2.9% dw, 0.1-0.2% dw, 0.9-110 ng g(-1) dw and 6.2-1200 ng g(-1) dw, respectively. Correlation analysis of BC (r = 0.26-0.89) and TOC (r = 0.06-0.69) revealed a stronger association with studied compounds. The sedimentary depositional fluxes (D) for ∑OCPs and ∑26PCBs were calculated as 1.7 and 4.9 tons yr(-1), respectively. In the coastal belt of Pakistan, sedimentary mass inventories (I) indicated the presence of 13 and 37 metric tons of ∑OCPs and ∑26PCBs, respectively. Copyright © 2014 Elsevier Ltd. All rights reserved.

Distributions of total organic carbon (TOC), black carbon (BC), and polycyclic aromatic hydrocarbons (PAH) were investigated in different particle size fractions for four Norwegian harbor sediments. The total PAH (16-EPA) concentrations ranged from 2 to 113 mg/kg dry weight with the greatest fraction of PAH mass in the sand fraction for three of the four sediments. TOC contents ranged from 0.84% to 14.2% and BC contents from 0.085% to 1.7%. This corresponds to organic carbon (OC = TOC - BC) contents in the range of 0.81-14% and BC:TOC ratios of 1.3-18.1%. PAH isomer ratios suggested that the PAH in all four sediments were of pyrogenic origin. Furthermore, stronger correlations between PAH versus BC (r2 = 0.85) than versus OC (r2 = 0.15) were found. For all size fractions and bulk sediments, the PAH-to-BC ratios for the total PAHs were on average 6+/-3 mg PAH/g BC. These results suggest that PAH distributions were dominated by the presence of BC, rather than OC. As sorption to BC is much stronger than sorption to OC, this may result in significantly lower dissolved concentrations of PAH than expected on the basis of organic carbon partitioning alone.

Wildfires and incomplete combustion of fossil fuel produce large amounts of black carbon. Black carbon production and transport are essential components of the carbon cycle. Constraining estimates of black carbon exported from land to ocean is critical, given ongoing changes in land use and climate, which affect fire occurrence and black carbon dynamics. Here, we present an inventory of the concentration and radiocarbon content (Delta C-14) of particulate black carbon for 18 rivers around the globe. We find that particulate black carbon accounts for about 15.8 +/- 0.9% of river particulate organic carbon, and that fluxes of particulate black carbon co-vary with river-suspended sediment, indicating that particulate black carbon export is primarily controlled by erosion. River particulate black carbon is not exclusively from modern sources but is also aged in intermediate terrestrial carbon pools in several high-latitude rivers, with ages of up to 17,000 C-14 years. The flux-weighted C-14 average age of particulate black carbon exported to oceans is 3,700 +/- 400 C-14 years. We estimate that the annual global flux of particulate black carbon to the ocean is 0.017 to 0.037 Pg, accounting for 4 to 32% of the annually produced black carbon. When buried in marine sediments, particulate black carbon is sequestered to form a long-term sink for CO2.

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, corresponding to 1.5-3.3% of the anthropogenic CO uptake by the ocean.© 2022. The Author(s).

A portion of the charcoal and soot produced during combustion processes on land (e.g., wildfire, burning of fossil fuels) enters aquatic systems as dissolved black carbon (DBC). In terms of mass flux, rivers are the main identified source of DBC to the oceans. Since DBC is believed to be representative of the refractory carbon pool, constraining sources of marine DBC is key to understanding the long-term persistence of carbon in our global oceans. Here, we use compound-specific stable carbon isotopes (δC) to reveal that DBC in the oceans is ~6‰ enriched in C compared to DBC exported by major rivers. This isotopic discrepancy indicates most riverine DBC is sequestered and/or rapidly degraded before it reaches the open ocean. Thus, we suggest that oceanic DBC does not predominantly originate from rivers and instead may be derived from another source with an isotopic signature similar to that of marine phytoplankton.

Aim  To provide insights concerning changes in fire regime in north‐eastern Cambodia over the course of the Holocene, and discuss implications of these long‐term data for fire management in the present day.

东西伯利亚陆架作为全球最为宽浅的陆架之一，在全球变暖和北极快速变化背景下，受海冰减少、冻土退化、径流增加和海岸侵蚀加剧等因素的影响，该区沉积有机碳的来源、输运和埋藏发生着显著变化，且不同地区之间差异显著。东西伯利亚海西部和拉普捷夫海沉积有机碳以陆源贡献为主，海岸侵蚀作用提高了冻土碳的入海通量，对气候变化具正反馈效应；楚科奇海具有较高的有机碳埋藏效率，季节性海冰变化对有机碳的源汇有直接的影响。受沉积水动力作用影响，陆源沉积有机碳从勒拿河河口输运到陆架边缘需3 000~4 000年，不同类型有机碳存在显著的分异和降解。陆架有机碳埋藏具有显著的时空差异，大量高活性的冻土碳由陆向海的快速沉积对于北极土壤碳库的稳定性、水生环境有机碳的矿化及CO₂的排放等方面具有重要的意义。今后该区的研究应加强综合地球化学指标和典型有机分子碳同位素等手段的应用，开展区域对比研究，重视海冰过程与有机碳源汇的联系，结合区域碳循环多模型集成，从现代过程与地质记录、替代指标与数值模拟相结合的角度去认识不同时间尺度快速气候变化下的有机碳源汇格局及其气候环境效应。

The East Siberian Arctic Shelf （ESAS） is one of the widest and shallowest continental shelves in the world. In the context of the global warming and rapid Arctic changes， the sources， transport and burial of sedimentary Organic Carbon （OC） in this area have experienced significant changes with spatial heterogeneity， which could be related to the sea-ice reduction， permafrost degradation， increased runoff and intensified coastal erosion. The sedimentary OC is mainly contributed by Terrestrial Organic Carbon （TerrOC） in the western East Siberian Sea and the Laptev Sea， and the coastal erosion increases the flux of Permafrost Carbon （PF/C） with a positive climate feedback effect. The Chukchi Sea has high organic carbon burial efficiency， where the seasonal variation of sea ice has direct effect on the source and sink of OC. Under the influence of hydrodynamic sorting， the cross-shelf transport times of TerrOC from the Lena estuary to the shelf edge requires approximately 3 000～4 000 years， by coupling with a significant geochemical differentiation and degradation. There existed spatio-temporal variation for the OC burial on the ESAS， and the large amount and rapid deposition of highly-reactive PF/C from the land to the sea could have important significance for the Arctic soil carbon， the OC mineralization in the aquatic environment， and CO₂ outgassing. The following research should strengthen the application of the comprehensive geochemical indices and the compound-specific isotope method， emphasizing the relation between the sea-ice and the sources and sink of the OC. By coupling with the models of regional carbon cycle， we should emphasize the integration of the modern process and geological records， proxy records with the numerical simulation， which is necessary to better understand the sources and sink of sedimentary OC and the climate and environmental effect from the varied timescales.

Rivers are the major carriers of dissolved black carbon (DBC) from land to ocean; the sources of DBC during its continuous transformation and cycling in the ocean, however, are not well characterized. Here, we present new carbon isotope data for DBC in four large and two small mountainous rivers, the Yangtze and Yellow river estuaries, the East China Sea and the North Pacific Ocean. We found that the carbon isotope signatures of DBC are relatively homogeneous, and the DBC C ages in rivers are predominantly young and increase during continuous transport and cycling in the ocean. The results of charcoal leaching experiments indicate that DBC is released from charcoal and degraded by bacteria. Our study suggests that riverine DBC is labile and respired during transport and mixing into the ocean and that residual DBC is cycled and aged on the same time scales as bulk DOC in the ocean.