Black Carbon Deposition Research Articles

A darker cryosphere in a warming world

Dust and black carbon deposition in high-mountain Asia darkens snow and ice, increases sunlight absorption and causes melt — a reinforcing feedback. Now research shows the increasing importance of dust over black carbon at higher altitude, and the sensitivity of aerosol transport and delivery to Arctic sea-ice melt.

Mass concentration and origin of black carbon in spring snow on glaciers in the Alaska Range

Black carbon (BC) is one of the light-absorbing particles that reduce the albedo of snow surfaces. Snow samples were taken from the surface of three glaciers in the Alaska Range in mid-April 2017. The BC size distribution and concentration were analyzed with a laser-induced incandescence (LII) method. The BC concentration of the snow samples was 1–6 μg L−1 and 0.5–3.1 μg L−1 at a depth of 0–2 cm (surface) and 2–10 cm (subsurface), respectively. These values are comparable to other Arctic areas and are considered to be the Alaskan background level. The BC concentrations are 0.5% of those of insoluble solid particles (ISPs) measured using an electrical sensing zone method. The surface albedo change due to BC and other ISPs concentrations was estimated to be 0.004–0.007 for the snow surface in April. The ablation at the observation sites on Gulkana Glacier would be 1.2% larger in the ablation season due to black carbon deposition. The chemical transport model revealed that 17%–34% of BC originates from biomass burning in Asia and Siberia, and 60% of BC originates from China in this study.

Seasonal Variation of Wet Deposition of Black Carbon in Arctic Alaska

AbstractBlack carbon (BC) aerosol deposited in and onto Arctic snow increases the snow's absorption of sunlight and accelerates snowmelt. Wet removal of BC from the atmosphere plays a key role in determining its abundance in the Arctic atmosphere and in Arctic snow. However, this process is poorly understood, mainly due to the scarcity of relevant measurements. To study wet deposition of BC, we made measurements of mass concentration of BC in snow and rain (CMBC) and of BC in air (MBC) with high accuracy (16% and 10%, respectively) at the Barrow Atmospheric Baseline Observatory, Alaska, from July 2013 to August 2017 and analyzed them along with routinely measured meteorological parameters from Barrow. Monthly mean MBC near the surface and CMBC were poorly correlated from midwinter to early spring, when CMBC was close to the annual median while MBC was at its annual peak. Seasonal variations in the altitude distribution of MBC may lead to these differences in seasonal variation of MBC near the surface and CMBC. About 50% of the annual wet deposition of BC occurred in the 3 months of summer, associated with high values of total precipitation and BC originating from biomass burning. Size distributions of BC in snow and rain were stable throughout the year, suggesting that the size distribution of BC in the lower troposphere was similarly stable. Calculations by two global models reproduced the observed seasonal variations of CMBC and showed that BC from biomass burning dominated CMBC in summer.

An Overview of Snow Albedo Sensitivity to Black Carbon Contamination and Snow Grain Properties Based on Experimental Datasets Across the Northern Hemisphere

Black carbon (BC) deposition in snow can trigger a significant reduction in snow albedo and accelerate snowmelt. As a result, numerous snow surveys have performed to measure BC concentrations in snow across the polar regions, the Tibetan Plateau, and other high-mountain regions. This review is aimed to synthesize the current progresses of the potential feedbacks of snow albedo and its sensitivity by BC in snow across the Northern Hemisphere. Generally, BC concentrations in snow are highest in the mid-latitudes of Northern China and North America, and reduce toward higher latitudes (e.g., Greenland and the rest of the Arctic). We found that the snow albedo reduction attributed to low BC contamination (< 20 ng g−1) in older snow (200 μm snow grains) is 1.2%, compared with 0.6% in fresh snow (50 μm snow grains). Non-spherical snow grains exhibit a significantly lower snow albedo reduction (2–6%) due to BC contamination compared with spherical snow grains with 100–500 ng g−1 of BC in the snowpack. Snow–BC–internal mixing reduces the snow albedo (< 10%) more substantially than does external mixing in the case of 50–200 μm snow grains and a given BC concentration (< 2000 ng g−1). Besides the BC and other light-absorbing particles (LAPs), the mixing state of LAPs in snow, snow grain properties, and the scavenging\washing effects are also major challenges in determining snow albedo, which need to be further investigated on a global scale.

The Post-Wildfire Impact of Burn Severity and Age on Black Carbon Snow Deposition and Implications for Snow Water Resources, Cascade Range, Washington

AbstractWildfires in the snow zone affect ablation by removing forest canopy, which enhances surface solar irradiance, and depositing light absorbing particles [LAPs, such as black carbon (BC)] on the snowpack, reducing snow albedo. How variations in BC deposition affects post-wildfire snowmelt timing is poorly known and highly relevant to water resources. We present a field-based analysis of BC variability across five sites of varying burn age and burn severity in the Cascade Range, Washington State, United States. Single particle soot photometer (SP2) analyses of BC snow concentrations were used to assess the impact of BC on snow albedo, and radiative transfer modeling was used to estimate the radiative effect of BC on snowmelt. Results were compared to Snowpack Telemetry (SNOTEL) data from one site that burned in 2012 and another in a proximal unburned forest. We show that post-wildfire forests provide a significant source of BC to the snowpack, and this effect increases by an order of magnitude in regions of high versus low burn severity, and decreased by two orders of magnitude over a decade. There is a shift in the timing of snowmelt, with snow disappearance occurring on average 19 ± 9 days earlier post-wildfire (2013–19) relative to pre-wildfire (1983–2012). This study improves understanding of the connection between wildfire activity and snowmelt, which is of high relevance as climate change models project further decreases in snowpack and increases in wildfire activity in the Washington Cascades.

Source attribution of Arctic black carbon and sulfate aerosols and associated Arctic surface warming during 1980–2018

Abstract. Observations show that the concentrations of Arctic sulfate and black carbon (BC) aerosols have declined since the early 1980s. Previous studies have reported that reducing sulfate aerosols potentially contributed to the recent rapid Arctic warming. In this study, a global aerosol–climate model (Community Atmosphere Model, version 5) equipped with Explicit Aerosol Source Tagging (CAM5-EAST) is applied to quantify the source apportionment of aerosols in the Arctic from 16 source regions and the role of aerosol variations in affecting changes in the Arctic surface temperature from 1980 to 2018. The CAM5-EAST simulated surface concentrations of sulfate and BC in the Arctic had a decrease of 43 % and 23 %, respectively, in 2014–2018 relative to 1980–1984 mainly due to the reduction of emissions from Europe, Russia and local Arctic sources. Increases in emissions from South and East Asia led to positive trends in Arctic sulfate and BC in the upper troposphere. All aerosol radiative impacts are considered including aerosol–radiation and aerosol–cloud interactions, as well as black carbon deposition on snow- and ice-covered surfaces. Within the Arctic, sulfate reductions caused a top-of-atmosphere (TOA) warming of 0.11 and 0.25 W m−2 through aerosol–radiation and aerosol–cloud interactions, respectively. While the changes in Arctic atmospheric BC has little impact on local radiative forcing, the decrease in BC in snow and ice led to a net cooling of 0.05 W m−2. By applying climate sensitivity factors for different latitudinal bands, global changes in sulfate and BC during 2014–2018 (with respect to 1980–1984) exerted a +0.088 and 0.057 K Arctic surface warming, respectively, through aerosol–radiation interactions. Through aerosol–cloud interactions, the sulfate reduction caused an Arctic warming of +0.193 K between the two time periods. The weakened BC effect on snow–ice albedo led to an Arctic surface cooling of −0.041 K. The changes in atmospheric sulfate and BC outside the Arctic produced a total Arctic warming of +0.25 K, the majority of which is due to the midlatitude changes in radiative forcing. Our results suggest that changes in aerosols over the midlatitudes of the Northern Hemisphere have a larger impact on Arctic temperature than other regions through enhanced poleward heat transport. The combined total effects of sulfate and BC produced an Arctic surface warming of +0.297 K, explaining approximately 20 % of the observed Arctic warming since the early 1980s.

Twentieth Century Black Carbon and Dust Deposition on South Cascade Glacier, Washington State, USA, as Reconstructed From a 158‐m‐Long Ice Core

AbstractLight absorbing particles (LAPs) include black carbon (BC) and mineral dust and are of interest due to their positive radiative forcing and contribution to albedo reductions and snow and glacier melt. This study documents historic BC and dust deposition as well as their effect on albedo on South Cascade Glacier (SCG) in Washington State (USA) through the analysis of a 158‐m (139.5‐m water equivalent [w.e.]) ice core extracted in 1994 and spanning the period 1840–1991. Peak BC deposition occurred between 1940 and 1960, when median BC concentrations were 16 times higher than background, likely dominated by domestic coal and forest fire emissions. Post 1960 BC concentrations decrease, followed by an increase from 1977 to 1991 due to melt consolidation and higher emissions. Differences between the SCG record and BC emission inventories, as well as ice core records from other regions, highlight regional differences in the timing of anthropogenic and biomass BC emissions. Dust deposition on SCG is dominated by local sources and is variable throughout the record. Albedo reductions from LAP are dominated by dust deposition, except during high BC deposition events from forest fires and during 1940–1960 when BC and dust similarly contribute to albedo reductions. This study furthers understanding of the factors contributing to historical snowmelt and glacier retreat in the Cascades and demonstrates that ice cores retrieved from temperate glaciers have the potential to provide valuable records of LAP deposition.

Effects of black carbon mitigation on Arctic climate

Abstract. We use the ECHAM-HAMMOZ aerosol-climate model to assess the effects of black carbon (BC) mitigation measures on Arctic climate. To this end we constructed several mitigation scenarios that implement all currently existing legislation and then implement further reductions of BC in a successively increasing global area, starting from the eight member states of the Arctic Council, expanding to its active observer states, then to all observer states, and finally to the entire globe. These scenarios also account for the reduction of the co-emitted organic carbon (OC) and sulfate (SU). We find that, even though the additional BC emission reductions in the member states of the Arctic Council are small, the resulting reductions in Arctic BC mass burdens can be substantial, especially in the lower troposphere close to the surface. This in turn means that reducing BC emissions only in the Arctic Council member states can reduce BC deposition in the Arctic by about 30 % compared to the current legislation, which is about 60 % of what could be achieved if emissions were reduced globally. Emission reductions further south affect Arctic BC concentrations at higher altitudes and thus only have small additional effects on BC deposition in the Arctic. The direct radiative forcing scales fairly well with the total amount of BC emission reduction, independent of the location of the emission source, with a maximum direct radiative forcing in the Arctic of about −0.4 W m−2 for a global BC emission reduction. On the other hand, the Arctic effective radiative forcing due to the BC emission reductions, which accounts for aerosol–cloud interactions, is small compared to the direct aerosol radiative forcing. This happens because BC- and OC-containing particles can act as cloud condensation nuclei, which affects cloud reflectivity and lifetime and counteracts the direct radiative forcing of BC. Additionally, the effective radiative forcing is accompanied by very large uncertainties that originate from the strong natural variability of meteorology, cloud cover, and surface albedo in the Arctic. We further used the TM5-FASST model to assess the benefits of the aerosol emission reductions for human health. We found that a full implementation in all Arctic Council member and observer states could reduce the annual global number of premature deaths by 329 000 by the year 2030, which amounts to 9 % of the total global premature deaths due to particulate matter.

Relative contribution of mineral dust versus black carbon to Third Pole glacier melting

Large-scale glaciers in the Third Pole are experiencing significant thinning and retreat, partly due to the increased deposition of black carbon (BC) and mineral dust (MD). At present, BC is generally considered a more important contributing factor than MD to glacier melting. Based on a deep analysis of published data, the relative contribution of MD versus BC to snow/ice melting increases rapidly, because BC is more likely than MD to be discharged during the melting process. As a result, the contribution of MD to glacier melting is comparable to or even higher than that of BC when the glacier surface appears as aged snow and bare ice. The importance of MD to glacier melting must therefore be emphasized in the water tower of Asia.

Editorial: Atmosphere—Cryosphere Interaction in the Arctic, at High Latitudes and Mountains With Focus on Transport, Deposition, and Effects of Dust, Black Carbon, and Other Aerosols

Editorial: Atmosphere—Cryosphere Interaction in the Arctic, at High Latitudes and Mountains With Focus on Transport, Deposition, and Effects of Dust, Black Carbon, and Other Aerosols

Black carbon in surface soil of the Himalayas and Tibetan Plateau and its contribution to total black carbon deposition at glacial region.

At present, the glaciers in the Himalayas and the Tibetan Plateau (HTP) are retreating partly due to albedo reduction caused by deposited light-absorbing impurities such as mineral dust (MD) and black carbon (BC). Because BC also exists widely in MD from surface soil, it is necessary to further evaluate the contribution of BC from MD to the total BC at glacier region. This will help to improve the study of BC sources by considering the relative contributions from MD and direct combustion sources. Therefore, in this study, concentrations of total organic carbon (TOC) and fine particles of BC from 43 surface soil samples of the HTP were investigated. The contribution of BC from MD to total BC deposited at the glacier region was evaluated. The results showed strong correlations between TOC and BC of studied samples (R2 = 0.70, p < 0.01), suggesting that they have similar sources and activity characteristics. The average BC concentration of studied samples was 2.02 ± 1.55 mg g-1, much lower than those of particles deposited at the glacier region and other regions with high soil TOC concentration. The contributions of BC from MD to total surface BC at two glaciers of the inner HTP (Zhadang and Xiaodongkemadi) were 17.66 ± 10.84% and 20.70 ± 16.35%, respectively. Therefore, the contribution of MD to glacier melting of the HTP is higher than that of previously assumed after BC coming along with MD is considered. Because MD concentration is higher at north and west part of the HTP, the contributions of MD at these glacier regions should be larger than previously assumed.

Atmospheric sulfur and nitrogen deposition in the Athabasca oil sands region is correlated with foliar nutrient levels and soil chemical properties

The oil extraction industry and human activity in north eastern Alberta has been growing steadily since the 1960’s and is a source of air pollution. In the late 1990’s the Wood Buffalo Environmental Association was established to monitor air quality for both public and environmental health. A primary environmental concern was soil acidification caused by sulfur (S) and nitrogen (N) deposition. A network of forest health monitoring (FHM) sites was established in dry jack pine ecosystems to serve as an early indicator of negative impacts. A sampling campaign was executed in 2011 and this study examines soil properties and foliar nutrients in the context of measured and modeled acid deposition. Total N (TN), SO42−, pH, base cation to aluminum ratio (BC:Al), and base saturation (% BS) are reported for the organic layer (LFH) and 3 depths in the mineral soil, while foliar nutrients were analysed from current annual growth in jack pine needles. Atmospheric deposition of S, N, BC, and potential acid input (PAI) in the study area was recently provided by Edgerton et al. (2020) and soil and foliar chemistry was evaluated based on deposition estimates and measurements. Inverse distance weighting was used to examine spatial patterns and regression analysis was used to quantify relationships between variables. The results indicated that S deposition is spatially correlated with foliar SO42− concentration, and LFH SO42−, but not mineral topsoil (0–5 cm) SO42−. Nitrogen deposition was spatially correlated with foliar N concentration, but not LFH or topsoil TN indicating potential uptake by the foliage or rapid uptake by roots in the LFH layer. High BC deposition in the same areas with the highest potential acid inputs (PAI) did not correlate significantly with changes in soil pH. However, LFH pH was significantly related to dry NH3 deposition, which has not been reported previously and requires further investigation.

Deposition of Organic and Black Carbon: Direct Measurements at Three Remote Stations in the Himalayas and Tibetan Plateau

AbstractCarbonaceous matter in the atmosphere has an important influence on climate change. Currently, the deposition of carbonaceous matter is one of the largest uncertainties in the climate system. This phenomenon is common in remote regions, such as the Himalayas and Tibetan Plateau. In this study, for the first time, we reported in situ measurements of wet and dry deposition rates of carbonaceous matter at three remote stations: Nam Co, Lulang, and Everest. The results showed that the annual wet deposition rates of water‐insoluble organic carbon (WIOC) and black carbon (BC) were 60.2 and 5.8 mg·m−2·year−1, 330 and 34.6 mg·m−2·year−1, and 47.0 and 2.6 mg·m−2·year−1 at the Nam Co, Lulang, and Everest stations, respectively. Seasonal variations in the wet deposition rates of WIOC and BC were controlled by precipitation amount and their atmospheric concentrations. In addition, the wet scavenging ratios of WIOC and BC at Nam Co Station were close to those observed in other remote areas. The total BC deposition at Nam Co Station (15.3 mg·m−2·year−1) was higher than that from chemical transport models, implying a dominant role of dry deposition of BC in the total deposition at this station and an urgent need to improve the aerosol deposition in models for the Himalayas and Tibetan Plateau. It was found that the deposition rates of carbonaceous matter in the Himalayas and Tibetan Plateau had large spatial variation; thus, high‐resolution models need to be applied in the future.

Deposition of ionic species and black carbon to the Arctic snowpack: combining snow pit observations with modeling

Abstract. Although aerosols in the Arctic have multiple and complex impacts on the regional climate, their removal due to deposition is still not well quantified. We combined meteorological, aerosol, precipitation, and snowpack observations with simulations to derive information about the deposition of sea salt components and black carbon (BC) from November 2011 to April 2012 to the Arctic snowpack at two locations close to Ny-Ålesund, Svalbard. The dominating role of sea salt and the contribution of dust for the composition of atmospheric aerosols were reflected in the seasonal composition of the snowpack. The strong alignment of the concentrations of the major sea salt components in the aerosols, the precipitation, and the snowpack is linked to the importance of wet deposition for transfer from the atmosphere to the snowpack. This agreement was less strong for monthly snow budgets and deposition, indicating important relocation of the impurities inside the snowpack after deposition. Wet deposition was less important for the transfer of nitrate, non-sea-salt sulfate, and BC to the snow during the winter period. The average BC concentration in the snowpack remains small, with a limited impact on snow albedo and melting. Nevertheless, the observations also indicate an important redistribution of BC in the snowpack, leading to layers with enhanced concentrations. The complex behavior of bromide due to modifications during sea salt aerosol formation and remobilization in the atmosphere and in the snow were not resolved because of the lack of bromide measurements in aerosols and precipitation.

Optical determination of black carbon mass concentrations in snow samples: A new analytical method

Black carbon (BC) aerosols in the atmosphere strongly affect direct radiative forcing and climate, not only while suspended in the atmosphere but also after deposition onto high albedo surfaces. Snow surfaces are especially sensitive to BC deposition, because of their high surface albedo and additional positive feedbacks further enhance faster snowpack melting caused by BC deposition, resulting in modifications in water resources and recession of glaciers. For the analysis of BC deposition on snow, a precise quantification of BC mass is needed. Instead, optical methods have the potential of quantifying only BC, based on its characteristic spectral absorption. Commercial optical transmissometers commonly use quartz filters to filter BC and measure its optical attenuation. They are calibrated for the determination of BC mass concentrations in air, but not adapted or calibrated for their determination in water or snowmelt samples. Additionally, they are generally calibrated using BC-simulating materials that are not representative of ambient BC particles.Here, a new analytical method is demonstrated for the quantitative determination of BC mass concentration in snow samples that considers filtering of melted snow with polycarbonate filters in a new device, and optical filter attenuation BC mass concentration measurement (880 nm). The attenuation can be obtained with any optical equipment that can measure the 880-nm attenuation of filters impacted with BC/snow impurities.This method has been calibrated using real diesel vehicle exhaust soot with well-known optical properties as reference material, yielding a multipoint calibration curve for common BC concentration levels in snow. The limits of detection (0.011 mg of BC), quantification (0.036 mg of BC) and reproducibility (96.39%) of this new analytical method have been determined. Real surface snow samples collected at different locations in “Los Andes” mountains of Chile were measured with this method given a BC concentrations ranged from 151 to 5987 μg kg−1.

Urban black carbon - source apportionment, emissions and long-range transport over the Brahmaputra River Valley

This research investigates whether the vehicular black carbon emissions originated in the North-Eastern city of Guwahati are transported over and in the Brahmaputra River Valley and the Himalayas. The total black carbon was apportioned between the fossil fuel and biomass burning by real-time measurements of black carbon concentrations at two distinct locations having different traffic volumes in 2016–17. The average observed BC concentrations were 20.58, 6.42, 3.50 and 5.29 μg/m3 at the low traffic location and 22.44, 17.14, 9.2 and 16.87 μg/m3 at the high traffic location in winter, pre-monsoon, monsoon and post-monsoon seasons, respectively. Temperature, wind speed, and solar radiation were found to have significant negative correlations with BC concentrations, while relative humidity had positive correlations. It was found that vehicles contributed over 85% of the ambient black carbon at both locations. Black carbon emission from this dominant source was estimated for 2018, which showed that from vehicles it increased to 0.44–0.55 Gg in 2018 from 0.29 to 0.33 Gg in 2011, which may result in the adverse impacts on the eco-sensitive Brahmaputra River Valley and the Himalayas. The transport and deposition of black carbon under different climatic seasons was modelled using HYSPLIT. The results showed that black carbon particulates are being transported and deposited all-round the year in the Himalayas and the surrounding region. Pre-monsoon and monsoon seasons contributed to the largest amounts of deposition, and a clear relation was found between deposition and rainfall. The total BC deposited in the Brahmaputra River Valley and the Himalayas during one year was 22,142.69 kg and 1566.53 kg with average deposition rates of 0.6452 μgm−2 day−1 and 0.0182 μgm−2 day−1, respectively.

Sources of black carbon in the atmosphere and in snow in the Arctic.

We systematically identify sources of black carbon (BC) in the Arctic, including BC in the troposphere, at surface and in snow, using tagged tracer technique implemented in a 3D global chemical transport model GEOS-Chem. We validate modeled BC sources (fossil fuel combustion versus biomass burning) against carbon isotope measurements at Barrow (Alaska), Zeppelin (Norway), Abisko (Sweden), Alert (Canada) and Tiksi (Russia) in the Arctic. The model reproduces the observed annual mean fraction of biomass burning (fbb, %) at the five sites within 20% and the observed and modeled monthly fbb values agree within a factor of two. Model results suggest that fossil fuel combustion is the major source of BC in the troposphere (50-94%, vary with sub-regions), at surface (55-68%) and in snow (58-69%) in the Arctic as annual mean, but biomass burning dominates at certain altitudes (600-800 hPa) and during periods of time between April to September. The model shows that BC in the troposphere, in deposition and in snow in different Arctic sub-regions have distinctively different sources and source regions. We find that long-range transport of Asian emissions has a stronger influence on BC in the atmosphere than on BC deposition. In contrast, contributions from Russian and European emissions are larger for BC deposition than for BC in the atmosphere. Specifically, Asian fossil fuel combustion emissions dominate BC loading in all Arctic sub-regions in both winter (Oct.-Mar., 35-54%) and summer (Apr.-Sep., 34-56%). For BC deposition, Siberian fossil fuel emissions are the largest contributors in Russia both in winter (62%) and summer (44%), and European fossil fuel emissions dominate in Ny-Ålesund (44% in winter) and Tromsø (71% in winter and 46% in summer). For BC deposition in the North American sector, Asian fossil fuel emissions are the largest contributors in winter (25-38%) and North American biomass burning emissions (38-72%) dominate in summer.

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.

Historical Black Carbon Reconstruction from the Lake Sediments of the Himalayan-Tibetan Plateau.

Black carbon (BC) is one of the major drivers of climate change, and its measurement in different environment is crucial for the better understanding of long-term trends in the Himalayan-Tibetan Plateau (HTP) as climate warming has intensified in the region. We present the measurement of BC concentration from six lake sediments in the HTP to reconstruct historical BC deposition since the pre-industrial era. Our results show an increasing trend of BC concurrent with increased anthropogenic emission patterns after the commencement of the industrialization era during the 1950s. Also, sedimentation rates and glacier melt strengthening influenced the total input of BC into the lake. Source identification, based on the char and soot composition of BC, suggests biomass-burning emissions as a major contributor to BC, which is further corroborated by open-fire occurrence events in the region. The increasing BC trend continues to recent years, indicating increasing BC emissions, mainly from South Asia.

Source attribution of black carbon affecting regional air quality, premature mortality and glacial deposition in 2000

Black carbon (BC) mitigation can reduce adverse environmental impacts on climate, air quality, human health, and water resource availability. To facilitate the identification of mitigation priorities, we use a state-of-the-science global chemistry-climate coupled model (AM3), with additional tagged BC tracers representing regional (East Asia, South Asia, Europe and North America) and sectoral (land transport, residential, industry) anthropogenic BC emissions to identify sources with the largest impacts on air quality, human health and glacial deposition. We find that within each tagged region, domestic emissions dominate BC surface concentrations and associated premature mortality (generally over 90%), as well as BC deposition on glaciers (∼40–95% across glaciers). BC emissions occurring within each tagged source region contribute roughly 1–2 orders of magnitude more to their domestic BC concentrations, premature mortality, and BC deposition on regional glaciers than that caused by the same quantity of BC emitted from foreign regions. At the sectoral level, the South Asian residential sector contributes ∼60% of BC associated premature mortality in South Asia and ∼40–60% of total BC deposited on southern Tibetan glaciers. Our findings imply that BC mitigation within a source region, particularly from East and South Asian residential sectors, will bring the largest reductions in BC associated air pollution, premature mortality, and glacial deposition.