Characteristics of methane and carbon dioxide in ice caves at a high-mountain glacier of China.

The exploration of the spatiotemporal distribution of greenhouse gas (GHG) exchange in the cryosphere (including ice sheet, glaciers, and permafrost) is important for understanding its future feedback to the atmosphere. Mountain glaciers and ice sheets may be potential sources of GHG emissions, but the magnitude and distribution of GHG emissions from glaciers and ice sheets remain unclear because observation data are lacking. In this study, in situ CH4 and CO2 and the mixing ratios of their carbon isotope signatures in the air inside an ice cave were measured, and CH4 and CO2 exchange in the meltwater of Laohugou glacier No. 12, a high-mountain glacier in an arid region of western China, was also analyzed and compared with the exchange in downstream rivers and a reservoir. The results indicated elevated CH4 mixing ratios (up to 5.7 ppm) and depleted CO2 (down to 168 ppm) in the ice cave, compared to ambient levels during field observations. The CH4 and CO2 fluxes in surface meltwater of the glacier were extremely low compared with their fluxes in rivers from the Tibetan Plateau (TP). CH4 and CO2 mixing ratios in the air inside the ice cave were mainly controlled by local meteorological conditions (air temperature, wind speed and direction) and meltwater runoff. The carbon isotopic compositions of CH4 and CO2 in the ice cave and terminus meltwater indicated δ13C-CH4 depletion compared to ambient air, suggesting an acetate fermentation pathway. The abundances of key genes for methanogenic archaea/genes encoding methyl coenzyme M reductase further indicated the production of CH4 by methanogenic archaea from the subglacial meltwater of high-mountain glaciers. The discovery of CH4 emissions from even small high-mountain glaciers indicates a more prevalent characteristic of glaciers to produce and release CH4 from the subglacial environment than previously believed. Nevertheless, further research is required to understand the relationship between this phenomenon and glacial dynamics in the third pole.

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.

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.

Displacement of mining vibrating screen obtained from acceleration based on improved S-G filter.

Vibration displacement is one of the key parameters in fault diagnosis of vibrating screens. Monitoring of acceleration signals of vibrating screens can be disturbed due to various factors such as on-site working conditions and equipment. In order to obtain accurate displacement signals of vibrating screen, the method for converting vibration acceleration to displacement based on improved Savitzky-Golay (S-G) filter is proposed. The Particle Swarm Optimization (PSO) algorithm is used to optimize the window length of the S-G filter with the fixed polynomial. The filters are cascaded to denoise the signals multiple times. The reasonable regularization parameter of the Smoothed Prior Approach (SPA) is calculated to remove the trend item from the acceleration signals. The vibration displacement is obtained by integrating the preprocessed acceleration data in the frequency domain. The results demonstrate that the objectivity of parameter selection of filter is improved, and the denoising effect is significant. The filtering effect of the filter is further improved after cascading. It becomes better as the number of stages of cascade increases. The vibration displacement can be obtained accurately by the proposed method. The vibration test platform is built to verify the correctness of the method.

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.

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.

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.

South Asian black carbon is threatening the water sustainability of the Asian Water Tower.

Long-range transport of black carbon from South Asia to the Tibetan plateau and its deposition on glaciers directly enhances glacier melt. Here we find South Asian black carbon also has an indirect effect on the plateau's glaciers shrinkage by acting to reduce the water supply over the southern Tibetan plateau. Black carbon enhances vertical convection and cloud condensation, which results in water vapor depletion over the Indian subcontinent that is the main moisture flux source for the southern Tibetan plateau. Increasing concentrations of black carbon causes a decrease in summer precipitation over the southern Tibetan plateau, resulting in 11.0% glacier deficit mass balance on average from 2007 to 2016; this loss rises to 22.1% in the Himalayas. The direct (accelerated melt) and indirect (mass supply decrease) effects of black carbon are driving the glacial mass decline of the so-called "Asian Water Tower".

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.

Molecular compositions, optical properties, and implications of dissolved brown carbon in snow/ice on the Tibetan Plateau glaciers.

Brown carbon (BrC)/water-soluble organic carbon (WSOC) plays a crucial role in glacier melting. A quantitative evaluation of the light absorption characteristics of WSOC on glacier melting is urgently needed, as the WSOC release from glaciers potentially affects the hydrological cycle, downstream ecological balance, and the global carbon cycle. In this work, the optical properties and composition of WSOC in surface snow/ice on four Tibetan Plateau (TP) glaciers were investigated using a three-dimensional fluorescence spectrometer and electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry. The total light-absorption of WSOC in snow/ice at 250-400 nm (ultraviolet region) and 400-600 nm (visible region) accounted for about 60.42% and 27.17% of the light absorption by the total organics, respectively. Two protein-like substances (PRLIS), one humic-like substance (HULIS), and one undefined species of chromophores in snow/ice on the TP glacier surfaces were identified. The lignins and lipids were the main compounds in the TP glaciers and were presented as CHO and CHNO molecules, while CHNOS molecules were only observed in the southeast TP glacier. The light absorption capacity of WSOC in snow/ice was mainly affected by their oxidizing properties. PRLIS and undefined species were closely linked to microbial sources and the local environment of the glaciers (lignins and lipids), while HULIS was significantly affected by anthropogenic emissions (protein/amino sugars). Radiative forcing (RF)-induced by WSOC relative to black carbon were accounted for about 11.62 ± 12.07% and 8.40 ± 10.37% in surface snow and granular ice, respectively. The RF was estimated to be 1.14 and 6.36 W m-2 in surface snow and granular ice, respectively, during the melt season in the central TP glacier. These findings contribute to our understanding of WSOC's impact on glaciers and could serve as a baseline for WSOC research in cryospheric science.

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.

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.

Photobleaching reduces the contribution of dissolved organic carbon to glacier melting in the Himalayas and the Tibetan Plateau.

Dissolved organic carbon (DOC) makes an important contribution to glacier melting in the Himalayas and the Tibetan Plateau (HTP). Photobleaching can effectively reduce the light absorption ability of DOC, further changing its impact on glacier melting, which is not yet well researched in the HTP. Therefore, snowpit samples from the Bayi, Ganglongjiama (GLJM), Jiemayangzong (JMYZ) and Demula (DML) glaciers were collected to study the influence of photobleaching on the light absorption ability of DOC and its impact on glacier melting. The results showed that the DOC concentration of snowpit samples, which was affected by the melting state and photobleaching, decreased from the northern HTP to the southern HTP. At an early stage of melting, the mass absorption cross-section value at 365 nm (MAC365) values showed a negative correlation with DOC concentrations in the snowpit at the JMYZ and DML glaciers, indicating that colored DOC tended to be concentrated in the snowpit during the melting process. With the aggravation of ablation, some snowpit samples in the GLJM and Bayi glaciers had both low concentrations and MAC365 values of DOC due to the reduced influence of photobleaching on the light absorption ability of DOC. Similarly, two fluorescence components (one protein-like component and one humic-like component) were identified in the extracted DOC at the JMYZ and DML glaciers, while those components were not detected in the GLJM glacier. Based on the sources of fluorescent DOC and five-day backward air mass trajectories, long-distance transport of pollutants from South Asia was an important source of snowpit DOC in the southern HTP. In this study, photobleaching can effectively remove colored and fluorescent DOC from snowpit samples in the HTP, further reducing the radiation forcing and glacier melting caused by DOC.

Mercury sources and physicochemical characteristics in ice, snow, and meltwater of the Laohugou Glacier Basin, China.

In this work, samples of surface snow, surface ice, snow pit and meltwater from the Laohugou Glacier No. 12 on the northern edge of Tibetan Plateau (TP) were collected during the summer of 2015. The average concentration of Hg in surface snow/ice was 22.41 ng L-1, while the percentage of dissolved mercury (HgD) was observed to be around 26%. An altitudinal magnification of Hg was not observed for surface snow; however, in contrast, a significant positive magnification of Hg with altitude was observed in the surface ice. A higher concentration of Hg corresponded with the dust layer of the snow pit. It was observed that about 42% of Hg was lost from the surface snow when the glacier was exposed to sunlight within the first 24 h indicating some Hg was emitted back to the atmosphere while some were percolated downwards. The result from the principal component analysis (PCA) showed that the sources of Hg in Laohugou Glacier No. 12 were from crustal and biomass burning. Finally, it was estimated that total export of Hg from the outlet river of Laohugou glacier No. 12 in the year 2015 was about 1439.46 g yr-1 with yield of 22.77 µg m2 yr-1. This study provides valuable insights for understanding the behavior of Hg in the glacier of the northern Tibetan Plateau.