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Tibetan Plateau (TP) is known as the water tower of Asia, and glaciers are solid reservoirs that can regulate the amount of water. Black carbon (BC), as one of the important factors accelerating glacier melting, is causing evident environmental effects in snow and ice. However, a systematical summary of the potential sources, analytical methods, distributions, and environmental effects of BC in snow and ice on the TP's glaciers is scarce. Therefore, this study drew upon existing research on snow and ice BC on glaciers of the TP to describe the detection methods and uncertainties associated with them to clarify the concentrations of BC in snow and ice and their climatic effects. The primary detection methods are the optical method, the thermal-optical method, the thermochemical method, and the single-particle soot photometer method. However, few studies have systematically compared the results of BC and this study found that concentrations of BC in different types of snow and ice varied by 1-3 orders of magnitude, which drastically affected the regional hydrologic process by potentially accelerating the ablation of glaciers by approximately 15% and reducing the duration of snow accumulation by 3-4 days. In general, results obtained from the various testing methods differ drastically, which limited the systematical discussion. Accordingly, a universal standard for the sampling and measurement should be considered in the future work, which will be beneficial to facilitate the comparison of the spatiotemporal features and to provide scientific data for the model-simulated climatic effects of BC., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

The deposition of light absorbing impurities (LAIs) (e.g., black carbon (BC), organic carbon (OC), mineral dust (MD)) on snow is an important attribution to accelerate snowmelt across the northern Xinjiang, China. At present, there is still a lack of understanding of the LAIs concentration, elution and enrichment process in snow cover over Xinjiang. Based on these, continuously sampling during two years carried out to investigate the concentrations, impacts and potential sources of LAIs in snow at Kuwei Station in the southern Altai Mountains. The average concentrations of BC, OC and MD in the surface snow were 2787 ± 2334 ng g -1 , 6130 ± 6127 ng g -1 , and 70.03 ± 62.59 μg g -1 , respectively, which dramatically increased along with snowmelt intensified, reflecting a significant enrichment process of LAIs at the snow surface. Besides, high LAIs concentrations also found in the subsurface and melting layers of the snowpit, reflecting the elution and redistribution of LAIs. With the simulation of the SNow ICe Aerosol Radiative model, BC was the main dominant factor in reducing snow albedo and radiative forcing (RF), its impact was more remarkable in the snowmelt period. The average contribution rates of BC, MD and BC + MD to snow albedo reduction increased by 20.0 ± 1.9%, 13.0 ± 0.2%, and 20.5 ± 2.3% in spring compared with that in winter; meanwhile, the corresponding average RFs increased by 15.8 ± 3.4 W m -2 , 4.7 ± 0.3 W m -2 and 16.4 ± 3.2 W m -2 , respectively. Changes in the number of snowmelt days caused by BC and MD decreased by 3.0 ± 0.4 d to 8.3 ± 1.3 d. It indicated that surface enrichment of LAIs during snow melting might accelerate snowmelt further. Weather Research and Forecasting Chemistry model showed that the resident emission was the main potential source of BC and OC in snow. This implied that the mitigation of intensive snowmelt needs to mainly reduce resident emission of LAIs in the future., Competing Interests: Declaration of competing interest The authors declare that there are no conflicts of interest., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Atmospheric aerosols are a branch of active research in recent decades. The deposition of light-absorbing substances on high-altitude glaciers causes substantial adverse impacts on the cryospheric environment, cryosphere-hydrology, and climate system. Although, the concentrations of water-soluble organic carbon (WSOC) in snow/ice on glaciers of Tibetan Plateau (TP) have been reported, their transfer processes and optical properties in the context of summer precipitation-atmosphere-snow-river water continuum are seldom studied. In this study, we have systematically examined some scientific issues associated with WSOC concentrations and light absorption properties of WSOC in various forms of samples from the Mt. Yulong region. Statistical results demonstrate that the spatial distribution of WSOC in the snow of Baishui glacier was heterogeneous. The average WSOC concentrations of each snowpit were significantly decreased, and its light-absorbing properties were significantly elevated with the time extension. Aerosol WSOC concentrations and light absorption have distinct spatial disparity and seasonal variation. Pre-monsoon and monsoon have the highest and lowest WSOC content, respectively. Whereas the light-absorbing properties present contrasting seasonal trends. Rivers of which runoff was supplied by glacier meltwater have significantly lower WSOC concentrations (e.g., 0.42 ± 0.03 mg L -1 ) compared with other forms of water bodies. Mass absorption cross-section of WSOC (MAC- WSOC ) in multiple snow and meltwater samples was significantly different and type-dependent. Atmospheric aerosol has the lowest MAC- WSOC value among the four types of samples, which was likely associated with exhaust emissions from private vehicles and tour buses. Statistical results indicated that the average AAE 330-400 values of various snow/ice samples are subequal. Snow of glaciers supplies a desirable platform for the deposition of gaseous materials which experienced long-range transport in high altitude zones. Biomass-burning emissions made an immense contribution to the WSOC deposition over the study area, as demonstrated by the distribution of active fire points. However, this preliminary study represents the first systematic investigation of WSOC deposition in southeastern TP. Further robust in-situ field investigations and laboratory measurements are urgently necessary to improve our understanding of the transfer process and optical property of WSOC., (Copyright © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

In order to investigate the compositions and wet deposition fluxes of trace elements and rare earth elements (REEs) in the precipitation of the southeastern edge of the Tibetan Plateau, 38 precipitation samples were collected from March to August in 2012 in an urban site of Lijiang city in the Mt. Yulong region. The concentrations of most trace elements and REEs were higher during the non-monsoon season than during the monsoon season, indicating that the lower concentrations of trace elements and REEs observed during monsoon had been influenced by the dilution effect of increased precipitation. The concentrations of trace elements in the precipitation of Lijiang city were slightly higher than those observed in remote sites of the Tibetan Plateau but much lower than those observed in the metropolises of China, indicating that the atmospheric environment of Lijiang city was less influenced by anthropogenic emissions, and, as a consequence, the air quality was still relatively good. However, the results of enrichment factor and principal component analysis revealed that some anthropogenic activities (e.g., the increasing traffic emissions from the rapid development of tourism) were most likely important contributors to trace elements, while the regional/local crustal sources rather than anthropogenic activities were the predominant contributors to the REEs in the wet deposition of Lijiang city. Our study was relevant not only for assessing the current status of the atmospheric environment in the Mt. Yulong region, but also for specific management actions to be implemented for the control of atmospheric inputs and the health of the environment for the future., (Copyright © 2016. Published by Elsevier B.V.)

Nitrate (NO3−) is a prominent atmospheric pollutant and a key chemical constituent of snow and ice, which plays a crucial role in the atmosphere and significantly impacts regional climate and environment conditions through a series of complex chemical processes. By summarizing the recent research progress on the nitrate chemical process (particularly on the isotopic measurements of NO3− (δ15N, Δ17O and δ18O)) in atmosphere and glacier snow, this study mainly investigated the chemical compositions and chemical processes, formation pathways, and photochemical reactions of nitrate in snow and atmosphere. Our results identified that the main ways of atmospheric nitrate formation are the hydrolysis of N2O5 and the reaction of ·OH with NO2; the spatial distribution of Δ17O and δ18O values of atmospheric nitrate have a significant latitudinal trend between 30° N–60° N; the study of stable isotopes (δ15N and δ18O) and the oxygen isotope anomaly (Δ17O) of nitrate have mainly been carried out over the densely populated and coastal mega cities; there exist significant gaps in the study of chemistry processes of nitrate in snow and ice and the air–snow interfaces across glaciated regions. This study provides a basic reference for more robust observations and research of nitrate in glacier areas in the future. [ABSTRACT FROM AUTHOR]

We evaluated the concentration, size and distribution, and temporal variation of insoluble dust micro-particles in the snow, rainfall and water taken from the areas surrounding the Mt. Yulong to define the characteristics of modern atmospheric dust deposition and the contributions of different dust sources. The mean mass concentration (4511 μg kg −1 ) of micro-particles with 0.57 < d < 26 μm, and the diameter (11.5 μm) of dust contained in the water bodies of the Mt. Yulong are roughly similar to those observed in other sites, implying that dust is primarily supplied through short-range transport from proximal source regions (several or hundreds of km distances). The mean mass concentrations of micro-particles with 0.57 < d < 26 μm is lower in the rainfall than in the snow and the river water, suggesting the rain water is an ideal source/carrier for detecting the characteristics of modern atmospheric micro-particles. Volume size distributions of micro-particles in the snow and water showed single modal structures having volume median diameters from 3 to 26 μm. Number concentrations of micro-particles in the snow were higher than that in the rainfall, the river water contains the least amount of micro-particles. Vertical profiles of the snowpits show that there is a strong lateral correlation among the dust peaks, indicating a regional uniformity of dust deposition and suitability of snow analysis for dust deposition. In addition, the bare rock of snow-free terrain in the Mt. Yulong region and the mineral particles from local rock weathering are also important sources for the dust deposition. [ABSTRACT FROM AUTHOR]

Black carbon (BC), dust, and organic carbon (OC) aerosols, when deposited onto the surface of glaciers, can absorb light and decrease the snow albedo. These impurities in snow are referred to as ILAIs (i.e., insoluble light absorbing impurities). Atmospheric chemical models have been extensively used to simulate the transport and deposition of atmospheric aerosols in glacierized areas. However, systematic investigations of ILAIs in snowpack of glaciers on the Tibetan Plateau (TP) are rare. In this study, observations of ILAIs in snow and simulations of ILAIs of atmospheric aerosol at surface over four glaciers on the TP have been analyzed. Strong correlation between BC and dust was found in surface aged-snow, and their correlation significantly varied with snowpit depth. BC and OC concentrations in snowpit tended to decrease with depth. Significant differences of ILAI concentrations among depth intervals reflect their diverse hydrophilicities, physiochemical properties and post-depositional processes in snowpit, offering important observational constraints on the related processes. Monthly variation of atmospheric ILAIs at surface over glaciers is characterized by distinct spatial heterogeneity. The statistical results show higher ILAI concentrations in the summer of 2015 than 2014, which is in qualitative agreement with CALIPSO observations, likely reflecting the effects of inter-annual variation of summer monsoon on snow ILAI loadings. Optical attenuation (ATN) of BC is gradually decreased with depth of snowpit, whereas the trend of mass absorption cross-section (MAC) of BC throughout the profile of snowpit is opposite to that of ATN. The scanning electron microscopy (SEM) imaging demonstrates that calcium and silicon rich particles dominate over biological, quartz and flying ash particles in the cryoconite, providing additional constraints on the sources of dust-in-snow and can facilitate better understanding of the physicochemical properties and climatic effects of particles in the glacial cryoconite. Unlabelled Image • The monthly trend of ILAIs is characterized by distinct spatial heterogeneity. • Snowpack BC and OC concentrations tended to decrease with snowpit depth. • Mass absorption cross-section (MAC) of BC throughout the profile of snowpit is increased. • Calcium and silicon-rich particles dominate over other particles in glacier cryoconite. [ABSTRACT FROM AUTHOR]

• Surface snow experiences post-depositional processes. • Snowpack in the accumulation period is a record of winter precipitation. • Wind is an crucial factor for isotopes in the accumulation period. • Isotopic exchange is the controlling factor for isotopes in the ablation period. Stable isotopes are useful for obtaining hydroclimatic and past environmental information. The record of stable isotopes in snow not only reflects the deposition condition but also provides information on post-depositional processes, which benefits ice core studies. In this study, δ 18O and δ D in new snow, surface snow and snowpack were measured to analyze deposited and post-depositional processes on a temperate glacier at the southeast margin of the Tibetan plateau. The results indicated that new snow and surface snow were relatively depleted in heavy isotopes during the post-monsoon period and enriched in heavy isotopes during the westerly and pre-monsoon period. Surface snow was enriched in 18O and D relative to new snow sampled during the same period. Isotopic homogenization was observed in May and June snowpack, illustrating the effect of melting on isotopes. The relatively low slope (<8) for the δ D– δ 18O line during the post-monsoon period and high slope (>8) during the westerly and pre-monsoon periods corresponded to temperature change. Although the vertical isotopic composition of snowpack sampled in April recorded the deposited information of winter precipitation, the post-depositional processes could have altered the isotopic composition of snow. During the accumulation period, wind drift was an crucial factor leading to abrupt isotopic modification in snow, which was verified using the energy-balance model and wind regime. During the ablation period, the decreasing trend of the slope and the gradual enrichment of 18O and D in the leaving snow mainly resulted from the isotopic exchange between liquid and solid water. The study enhanced our understanding of the controlling post-depositional processes on temperate glaciers. [ABSTRACT FROM AUTHOR]