Himalayas is barrier for transportation of light-absorbing particles from South Asia to inner Third Pole.

Through a comprehensive investigation into the historical profiles of black carbon derived from ice cores, the spatial distributions of light-absorbing impurities in snowpit samples, and carbon isotopic compositions of black carbon in snowpit samples of the Third Pole, we have identified that due to barriers of the Himalayas and remove of wet deposition, local sources rather than those from seriously the polluted South Asia are main contributors of light-absorbing impurities in the inner part of the Third Pole. Therefore, reducing emissions from residents of the Third Pole themselves is a more effective way of protecting the glaciers of the inner Third Pole in terms of reducing concentrations of light-absorbing particles in the atmosphere and on glaciers.

Stable Carbon Isotope Signatures of Carbonaceous Aerosol Endmembers in the Tibetan Plateau.

Carbonaceous aerosols play an important role in radiative forcing in the remote and climate-sensitive Tibetan Plateau (TP). However, the sources of carbonaceous aerosols to the TP remain poorly defined, in part due to the lack of regionally relevant data about the sources of carbonaceous aerosols. To address this knowledge gap, we present the first comprehensive analysis of the δ13C signatures of carbonaceous aerosol endmembers local to the TP, encompassing total carbon, water-insoluble particle carbon, and elemental carbon originating from fossil fuel combustion, biomass combustion, and topsoil. The δ13C signatures of these local carbonaceous endmembers differ from components collected in other regions of the world. For instance, fossil fuel-derived aerosols from the TP were 13C-depleted relative to fossil fuel-derived aerosols reported in other regions, while biomass fuel-derived aerosols from the TP were 13C-enriched relative to biomass fuel-derived aerosols reported in other regions. The δ13C values of fine-particle topsoil in the TP were related to regional variations in vegetation type. These findings enhance our understanding of the unique features of carbonaceous aerosols in the TP and aid in accurate source apportionment and environmental assessments of carbonaceous aerosols in this climate-sensitive region.

South and Southeast Asia controls black carbon characteristics of Meili Snow Mountains in southeast Tibetan Plateau.

South and Southeast Asia (SSA) emitted black carbon (BC) exerts potential effects on glacier and snow melting and regional climate change in the Tibetan Plateau. In this study, online BC measurements were conducted for 1 year at a remote village located at the terminus of the Mingyong Glacier below the Meili Snow Mountains. The Weather Research and Forecasting model coupled with Chemistry (WRF-Chem) was used to investigate the contribution and potential effect of SSA-emitted BC. In addition, variations in the light absorption characteristics of BC and brown carbon (BrC) were examined. The results indicated that the annual mean concentration of BC was 415 ± 372 ngm-3, with the highest concentration observed in April (monthly mean: 930 ± 484 ngm-3). BC exhibited a similar diurnal variation throughout the year, with two peaks observed in the morning (from 8:00 to 9:00 AM) and in the afternoon (from 4:00 to 5:00 PM), with even lower values at nighttime. At a short wavelength of 370 nm, the absorption coefficient (babs) reached its maximum value, and the majority of babs values were < 20 Mm-1, indicating that the atmosphere was not overloaded with BC. At the same wavelength, BrC substantially contributed to babs, with an annual mean of 25.2 % ± 12.8 %. SSA was the largest contributor of BC (annual mean: 51.1 %) in the study area, particularly in spring (65.6 %). However, its contributions reached 20.2 % in summer, indicating non-negligible emissions from activities in other regions. In the atmosphere, the SSA BC-induced radiative forcing (RF) over the study region was positive. While at the near surface, the RF exhibited a significant seasonal variation, with the larger RF values occurring in winter and spring. Overall, our findings highlight the importance of controlling BC emissions from SSA to protect the Tibetan Plateau against pollution-related glacier and snow cover melting.

Weak transport of atmospheric water-insoluble particulate carbon from South Asia to the inner Tibetan Plateau in the monsoon season.

Carbonaceous particles play a crucial role in atmospheric radiative forcing. However, our understanding of the behavior and sources of carbonaceous particles in remote regions remains limited. The Tibetan Plateau (TP) is a typical remote region that receives long-range transport of carbonaceous particles from severely polluted areas such as South Asia. Based on carbon isotopic compositions (Δ14C/δ13C) of water-insoluble particulate carbon (IPC) in total suspended particle (TSP), PM2.5, and precipitation samples collected during 2020-22 at the Nam Co Station, a remote site in the inner TP, the following results were achieved: First, fossil fuel contributions (ffossil) to IPC in TSP samples (28.60 ± 9.52 %) were higher than that of precipitation samples (23.11 ± 8.60 %), and it is estimated that the scavenging ratio of IPC from non-fossil fuel sources was around 2 times that from fossil fuel combustion during the monsoon season. The ffossil of IPC in both TSP and PM2.5 samples peaked during the monsoon season. Because heavy precipitation during the monsoon season scavenges large amounts of long-range transported carbonaceous particles, the contribution of local emissions from the TP largely outweighs that from South Asia during this season. The results of the IPC source apportionment based on Δ14C and δ13C in PM2.5 samples showed that the highest contribution of liquid fossil fuel combustion also occurred in the monsoon season, reflecting increased human activities (e.g., tourism) on the TP during this period. The results of this study highlight the longer lifetime of fossil fuel-sourced IPC in the atmosphere than that of non-fossil fuel sources in the inner TP and the importance of local emissions from the TP during the monsoon season. The findings provide new knowledge for model improvement and mitigation of carbonaceous particles.

Significant spatial variations of the atmospheric environment at remote site of the Tibetan Plateau - a case study on major ions of precipitation around Nam Co station.

Remote region is normally considered a receptor of long-range transported pollutants. Monitoring stations are important platforms for investigating the atmospheric environment of remote regions. However, the potential contribution of very local sources around these stations may produce important influences on its atmospheric environment, which is still barely studied. In this study, major ions of precipitation were investigated simultaneously at a typical remote station (Nam Co station) and other sites nearby on the Tibetan Plateau (TP) - the so-called "The Third Pole" in the world. The results showed that despite low values compared to those of other remote regions, the concentrations of major ions in precipitation of Nam Co station (e.g., Ca2+: 32.71 µeq/L; [Formula: see text]: 1.73 µeq/L) were significantly higher than those at a site around 2.2 Km away (Ca2+: 11.47 µeq/L; [Formula: see text]: 0.64 µeq/L). This provides direct evidence that atmospheric environment at Nam Co station is significantly influenced by mineral dust and pollutants emitted from surface soil and anthropogenic pollutants of the station itself. Therefore, numbers of other related data reported on the station are influenced. For example, the aerosol concentration and some anthropogenic pollutants reported on Nam Co station should be overestimated. Meanwhile, it is suggested that it is cautious in selecting sites for monitoring the atmospheric environment at the remote station to reduce the potential influence from local sources.

Dust dominates glacier darkening across majority of the Tibetan Plateau based on new measurements.

Rapid retreat and darkening of most glaciers in the Tibetan Plateau (TP) are enhanced by the deposition of light-absorbing particles (LAPs). Here, we provided new knowledge on the estimation of albedo reduction caused by black carbon (BC), water-insoluble organic carbon (WIOC), and mineral dust (MD), based on a comprehensive study of snowpit samples from ten glaciers across the TP collected in the spring of 2020. According to the albedo reductions caused by the three LAPs, the TP was divided into three sub-regions: the eastern and northern margins, Himalayas and southeastern TP, and western to inner TP. Our findings indicated that MD had a dominant role in causing snow albedo reductions across the western to inner TP, with comparable effects to WIOC but stronger effects than BC in the Himalayas and southeastern TP. BC played a more important role in the eastern and northern margins of the TP. In conclusion, the findings of this study emphasize not only the important role of MD in glacier darkening across majority of the TP but also the influence of the WIOC in enhancing glacier melting which indicates the dominant contribution of non-BC components in the LAP-related glacier melting of the TP.

Concentrations and light absorption properties of PM2.5 organic and black carbon based on online measurements in Lanzhou, China.

To elucidate the variations in mass concentrations of organic carbon (OC) and black carbon (BC) in PM2.5 and their light absorption characteristics in Lanzhou, we conducted one-year online measurements by using a newly developed total carbon analyzer (TCA08) coupled with an aethalometer (AE33) from July 2018 to July 2019. The mean OC and BC concentrations were 6.4 ± 4.4 and 2.0 ± 1.3 µg/m3, respectively. Clear seasonal variations were observed for both components, with winter having the highest concentrations, followed by autumn, spring, and summer. The diurnal variations of OC and BC concentrations were similar throughout the year, with daily two peaks occurring in the morning and evening, respectively. A relatively low OC/BC ratio (3.3 ± 1.2, n = 345) were observed, indicating that fossil fuel combustion was the primary source of the carbonaceous components. This is further substantiated by relatively low biomass burning contribution (fbiomass: 27.1% ± 11.3%) to BC using aethalometer based measurement though fbiomass value which increased significantly in winter (41.6% ± 5.7%). We estimated a considerable brown carbon (BrC) contribution to the total absorption coefficient (babs) at 370 nm (yearly average of 30.8% ± 11.1%), with a winter maximum of 44.2% ± 4.1% and a summer minimum of 19.2% ± 4.2%. Calculation of the wavelength dependence of total babs revealed an annual mean AAE370-520 value of 4.2 ± 0.5, with slightly higher values in spring and winter. The mass absorption cross-section of BrC also exhibited higher values in winter, with an annual mean of 5.4 ± 1.9 m2/g, reflecting the impact of emissions from increased biomass burning on BrC concentrations.

Importance of precipitation and dust storms in regulating black carbon deposition on remote Himalayan glaciers.

Black carbon (BC) can be transported over long distances and is an important trigger of climate warming and glacier melting at remote high mountains and polar regions. It is normally assumed that the variation of BC flux in remote regions is dominated by its emissions. However, after a comprehensive investigation of potential influencing factors on temporal variations of BC from ice cores of the Himalayas, this short communication shows that in addition to BC emissions, contributions from dust storms and precipitation are also important (up to 56% together) in regulating the variation of BC deposition flux and concentrations derived from remote Himalayan ice core measurements. Therefore, besides BC emissions, the influence of precipitation and BC transported by dust storms should also be considered to better quantify the lifetime and behavior of BC during its long-range transport from source to sink regions as well as to quantify the climatic effects of BC over remote Himalayan glaciers.

Dust dominates the summer melting of glacier ablation zones on the northeastern Tibetan Plateau.

Dust and black carbon (BC) can darken snow and ice surface and play pivotal roles in glacier mass loss. Thus, a quantitative assessment of their contributions to glacier summer melting is critical. During the summer of 2018, surface snow and ice were sampled, and the albedo and mass balance were continuously measured in the ablation zone of Laohugou Glacier No. 12 in the western Qilian Mountains. The physical properties of dust and BC were measured in the laboratory, and their impacts on glacier surface albedo reduction and melting were simulated. The results indicate that the ice surface in the ablation zone was enriched with substantial amounts of particles, and the average particle concentrations of these samples were hundreds of times higher than those of fresh snow. The BC mass absorption cross-sections (MACs) ranged from 3.1 m2 g-1 at 550 nm for dirty ice to 4.6 m2 g-1 for fresh snow, largely owing to meltwater percolation and particle collapse. The spectral variations in dust MACs were significantly different in the visible light bands and near-infrared bands from those in the other areas. Moreover, the two-layer surface energy and mass balance model with the new albedo parameterization formula was validated and agreed well with the experimental measurements of spectral albedo, broadband albedo, and mass balance. BC and dust combined resulted in 26.7 % and 54.4 % of the total mass loss on the cleaner and dirtier (particle enriched) surfaces in the ablation zone, respectively, compared to particle-free surfaces, and although both impurities played vital roles, dust was the more prominent factor in accelerating glacier melting on the northeastern Tibetan Plateau. This study emphasizes the importance of dust in cryosphere changes where Tibetan glaciers are strongly affected by Asian dust deposition.

Concentrations, sources, fluxes, and absorption properties of carbonaceous matter in a central Tibetan Plateau river basin.

Carbonaceous matter (CM) (such as water-insoluble organic carbon (WIOC), black carbon (BC), and water-soluble organic carbon (WSOC)) has a significant impact on the carbon cycle and radiative forcing (RF) of glacier. Precipitation samples and glacier's snow/ice samples (snowpit, surface snow, and granular ice) (Xiao dongkemadi Glacier) were collected at the Dongkemadi River Basin (DRB) in the central Tibetan Plateau (TP) between May and October 2016 to investigate the characteristics and roles of CM in the TP River Basin. WIOC, BC, and WSOC concentrations in precipitation were relatively higher than that in snowpit, but lower than that in surface snow/ice, with the wet deposition fluxes of 0.10 ± 0.002, 0.04 ± 0.001, and 0.12 ± 0.002 g C m-2 yr-1 at DRB, respectively. The positive matrix factorization model identified four major sources (biomass burning source, secondary precursors, secondary aerosol, and dust source) of CM in precipitation at DRB. Two source areas (South Asia and the interior of TP) contributing to the pollution at DRB were identified using a potential source contribution function model, a concentration-weighted trajectory method, and the back-trajectory model. Moreover, the light-absorption by WSOC in the ultraviolet region was 23.0%, 12.1%, and 3.4% relative to the estimated total light-absorption in precipitation, snowpit, and surface snow/ice, respectively. Optical indices analysis revealed that WSOC in snowpit samples presented higher molecular weight, while presented higher aromatic and higher molecule sizes in surface snow/ice and precipitation samples, respectively. RF by WSOC relative to that of BC was estimated to be 17.6 ± 17.6% for precipitation, 10.9 ± 5.8% for snowpit, and 10.7 ± 11.6% for surface snow/ice, respectively, during the melt season in the central TP River Basin. These results help us understand how CM affects glaciers, and they can be utilized to create policies and recommendations that efficiently reduce emissions.

Importance of local non-fossil sources to carbonaceous aerosols at the eastern fringe of the Tibetan Plateau, China: Δ14C and δ13C evidences.

Carbonaceous particles are an important radiative forcing agent in the atmosphere, with large temporal and spatial variations in their concentrations and compositions, especially in remote regions. This study reported the Δ14C and δ13C of total carbon (TC) and water-insoluble particulate carbon (IPC) of the total suspended particles (TSP) and PM2.5 at a remote site of the eastern Tibetan Plateau (TP), a region that is influenced by heavy air pollution from Southwest China. The average organic carbon and elemental carbon concentrations of TSP samples in this study were 3.20 ± 2.38 µg m-3 and 0.68 ± 0.67 µg m-3, respectively, with low and high values in summer and winter, respectively. The fossil fuel contributions of TC in TSP and PM2.5 samples were 18.91 ± 7.22% and 23.13 ± 12.52%, respectively, both of which were far lower than that in Southwest China, indicating the importance of non-fossil contributions from local sources. The δ13C of TC in TSP samples of the study site was -27.06 ± 0.96‰, which is between the values of long-range transported sources (e.g., Southwest China) and local biomass combustion emissions. Therefore, despite the contribution from the long-range transport of particles, aerosols emitted from local biomass combustion also have an important influence on carbonaceous particles at the study site. The findings of this work can be applied to other remote sites on the eastern TP and should be considered in related research in the future.

Composition and sources of heavy metals in aerosol at a remote site of Southeast Tibetan Plateau, China.

Knowledge of the elemental composition of aerosols at remote sites is important for evaluating the influence of anthropogenic activities. In this study, the elemental composition and sources of total suspended particles (TSP) at Yaze, a remote site in the southeastern Tibetan Plateau (TP), were investigated. The results showed that the mean elemental concentrations at Yaze were relatively low compared with those in other areas of the TP. Seasonal variations in the studied elements was characterized by low and high concentrations during the monsoon and non-monsoon periods, respectively. The enrichment factors (EFs) for some heavy metals at Yaze were slightly higher than those at Nam Co station (inland TP) but much lower than those at Mt. Yulong (southeastern TP) and in the Indian megacity of Delhi, indicating fewer anthropogenic influences at the study site relative to sites close to severely polluted regions. For the studied elements, three major sources were identified: crustal origins (e.g., Al and Fe), anthropogenic origins (e.g., Zn and Cd) and mixed origins (e.g., As and Bi). Further analysis by potential source contribution functions showed that the local TP was the primary source for elements of crustal origins. Correspondingly, the typical heavy metals were mainly attributed to pollution emitted from anthropogenic activities and transported over long-range from both South and Southeast Asia. This work demonstrates the transport of heavy metals from external sources to remote sites in the southeastern TP. These results are also useful for interpreting the historical profiles of heavy metals in the ice cores of the TP.

14C characteristics of organic carbon in the atmosphere and at glacier region of the Tibetan Plateau.

As an important component of carbonaceous aerosols (CA), organic carbon (OC) exerts a strong, yet insufficiently constrained perturbation of the climate. In this study, we reported sources of OC based on its natural abundance radiocarbon (14C) fingerprinting in aerosols and water-insoluble organic carbon (WIOC) in snowpits across the Tibetan Plateau (TP) - one of the remote regions in the world and a freshwater reservoir for billions of people. Overall, the proportions from 14C-based non-fossil fuel contribution (fnon-fossil) for OC in aerosols was 74 ± 10%, while for WIOC in snowpits was 81 ± 10%, both of which were significantly higher than that of elemental carbon (EC). These indicated sources of OC (WIOC) and EC were different at remote TP. Spatially, high fnon-fossil of WIOC of snowpit samples appeared at the inner part of the TP, indicating the important contribution of local non-fossil sources. Therefore, local non-fossil sources rather than long-range transportation OC dominants its total amount of the TP. In addition, the contribution of local non-fossil sourced WIOC increased during the monsoon period because heavy precipitation removed a high ratio of long-range transportation WIOC. The results of this study showed that not only OC and EC but also their different fuel sources should be treated separately in models to investigate their sources and atmospheric transportation.

An overestimation of light absorption of brown carbon in ambient particles caused by using filters with large pore size.

As an important component of carbonaceous particles, organic carbon (OC) plays a significant role in radiative forcing in the atmosphere. Recently, the warming effect of light-absorbing OC has been emphasized. Water-soluble organic carbon (WSOC) is commonly used as a surrogate to investigate the light absorption of OC. Thus far, filters with 0.45 µm (PS1) and 0.20 µm pore sizes (PS2) are both used to investigate the light absorption of WSOC, which may cause large divergent results. In this study, we found that the light absorption ability of WSOC treated with PS1 was higher than that of PS2 due to the extinction of suspended particles (e.g., black carbon) with particle size between 0.20 µm and 0.45 µm, although the concentrations of WSOC treated with PS1 and PS2 were very close. This phenomenon was more remarkable at visible wavelengths, resulting in an overestimation of the warming effect of WSOC by 9%-22% for aerosol samples treated by PS1, with the highest values occurring in samples heavily influenced by fossil fuel burning emissions. An overestimation of WSOC light absorption treated by PS1 occurred in the investigated ambient aerosol samples from three sites, so it may be a general phenomenon that also exists in other regions of the world. Therefore, to achieve the actual solar radiative forcing of OC in the atmosphere, it is recommended to use PS2 in the future, and reported data of WSOC treated by PS1 should be re-evaluated.

Organic aerosol compositions and source estimation by molecular tracers in Dushanbe, Tajikistan.

To elucidate the molecular composition and sources of organic aerosols in Central Asia, carbonaceous compounds, major ions, and 15 organic molecular tracers of total suspended particulates (TSP) were analyzed from September 2018 to August 2019 in Dushanbe, Tajikistan. Extremely high TSP concentrations (annual mean ± std: 211 ± 131 µg m-3) were observed, particularly during summer (seasonal mean ± std: 333 ± 183 µg m-3). Organic carbon (OC: 11.9 ± 7.0 µg m-3) and elemental carbon (EC: 5.1 ± 2.2 µg m-3) exhibited distinct seasonal variations from TSP, with the highest values occurring in winter. A high concentration of Ca2+ was observed (11.9 ± 9.2 µg m-3), accounting for 50.8% of the total ions and reflecting the considerable influence of dust on aerosols. Among the measured organic molecular tracers, levoglucosan was the predominant compound (632 ± 770 ng m-3), and its concentration correlated significantly with OC and EC during the study period. These findings highlight biomass burning (BB) as an important contributor to the particulate air pollution in Dushanbe. High ratios of levoglucosan to mannosan, and syringic acid to vanillic acid suggest that mixed hardwood and herbaceous plants were the main burning materials in the area, with softwood being a minor one. According to the diagnostic tracer ratio, OC derived from BB constituted a large fraction of the primary OC (POC) in ambient aerosols, accounting for an annual mean of nearly 30% and reaching 63% in winter. The annual contribution of fungal spores to POC was 10%, with a maximum of 16% in spring. Measurements of plant debris, accounting for 3% of POC, divulged that these have the same variation as fungal spores.

Overestimation of anthropogenic contribution of heavy metals in precipitation than those of aerosol samples due to different treatment methods.

Due to increased anthropogenic activities in recent decades, many heavy metal elements have been emitted into the atmosphere and transported to remote regions. The Enrichment factors (EFs) is a normally used method for evaluating the source of heavy metal elements. However, because of some flaws of this method (e.g., higher solubility of heavy metals elements than reference elements in dilute acid), the anthropogenic contributions of some heavy metal elements in the precipitation sample were overestimated. To address this issue, EFs of heavy metal elements of aerosol, precipitation and snowpit samples in a typical remote area of the Tibetan Plateau (TP) were compared. The results showed that the EF values of many heavy metal elements in precipitation and snowpit samples were close to that of aerosol samples treated with dilute acid but usually much higher than those of totally dissolved aerosol samples. Moreover, EF values of most heavy metal elements in the ice core at the margin of the TP were higher than those at central TP, indicating that signal of long-range transport anthropogenic emitted heavy metal elements is weak and may be covered by natural mineral dust sources at glacier region. Therefore, the threshold EF values for determining anthropogenic sources of heavy metal elements in precipitation and ice core samples should be higher than those of aerosols. This study provides new knowledge on investigating anthropogenic sources of heavy metals in precipitation samples at both the TP and other regions of the world.

Coupling of decreased snow accumulation and increased light-absorbing particles accelerates glacier retreat in the Tibetan Plateau.

Most glaciers in the Tibetan Plateau (TP) are experiencing dramatic retreat, which is resulting in serious environmental and ecological consequences. In addition to temperature increases, increased light-absorbing particles (LAPs) and decreased precipitation were proposed to, independently, play important roles in reducing glacier accumulation. Based on investigations of effect from an extremely low precipitation event in the TP and surrounding regions caused by La Niña from October 2020 to April 2021, a new mechanism was provided. It was shown that decreased precipitation during study period leaded to both low snow accumulation and high LAP concentrations in snow on glacier surfaces in the TP. This phenomenon will strongly enhance earlier and accelerated glacier melt in this critical region and needs to be considered in future related studies.