In this study, we used satellite observations to identify 10 typical dust-loading events over the Indian Himalayas. Next, the aerosol microphysical and optical properties during these identified dust storms are characterized using cotemporal in situ measurements over Mukteshwar, a representative site in Indian Himalayas. Relative to the background values, the mass of coarse particles (size range between 2.5 and 10 mu m) and the extinction coefficient were found to be enhanced by 400% (from 24 +/- 15 to 98 +/- 40 mu g/m3) and 175% (from 89 +/- 57 Mm-1 to 156 +/- 79 Mm-1), respectively, during these premonsoonal dust-loading events. Moreover, based on the air mass trajectory, these dust storms can be categorized into two categories: (a) mineral dust events (MDEs), which involve long-range transported dust plumes traversing through the lower troposphere to reach the Himalayas and (b) polluted dust events (PDEs), which involve short-range transported dust plumes originating from the arid western regions of the Indian subcontinent and traveling within the heavily polluted boundary layer of the Gangetic plains before reaching the Himalayas. Interestingly, compared to the background, the SSA and AAE decrease during PDEs but increase during MDEs. More importantly, we observe a twofold increase in black carbon concentrations and the aerosol absorption coefficient (relative to the background values) during the PDEs with negligible changes during MDEs. Consequently, the aerosol-induced snow albedo reduction (SAR) also doubles during MDEs and PDEs relative to background conditions. Thus, our findings provide robust observational evidence of substantial dust-induced snow and glacier melting over the Himalayas.

Indian monsoon circulation is the primary driver of the long-range transboundary mercury (Hg) pollution from South Asia to the Himalayas and Tibet Plateau region, yet the northward extent of this transport remains unknown. In this study, a strong delta Hg-202 signature overlapping was found between Lake Gokyo and Indian anthropogenic sources, which is an indicative of the Hg source regions from South Asia. Most of the sediment samples were characterized with relatively large positive Delta Hg-199 values (mean = 0.07 parts per thousand-0.44 parts per thousand) and small positive Delta Hg-200 values (mean = 0.03 parts per thousand-0.08 parts per thousand). Notably, the Delta Hg-199 values in the lake sediments progressively increased from southwest to northeast. Moreover, the Delta Hg-199 values peaked at Lake Tanglha (mean = 0.44 parts per thousand +/- 0.04 parts per thousand) before decreased at Lake Qinghai that is under the influence of the westerlies. Our results suggest that transboundary atmospheric transport could transport Hg from South Asia northwards to at least the Tanglha Mountains in the northern Himalaya-Tibet.

Throughcontinuous field observation and comprehensive chemicalanalysis, this study quantified the impacts of wildfire emissions,which have occurred repeatedly not only in a long-term period butalso with extensive spatial coverage, on the Himalayan ecosystem. Himalayas and Tibetan Plateau (HTP) is important forglobal biodiversityand regional sustainable development. While numerous studies haverevealed that the ecosystem in this unique and pristine region ischanging, their exact causes are still poorly understood. Here, wepresent a year-round (23 March 2017 to 19 March 2018) ground- andsatellite-based atmospheric observation at the Qomolangma monitoringstation (QOMS, 4276 m a.s.l.). Based on a comprehensive chemical andstable isotope (N-15) analysis of nitrogen compounds andsatellite observations, we provide unequivocal evidence that wildfireemissions in South Asia can come across the Himalayas and threatenthe HTP's ecosystem. Such wildfire episodes, mostly occurringin spring (March-April), not only substantially enhanced theaerosol nitrogen concentration but also altered its composition (i.e.,rendering it more bioavailable). We estimated a nitrogen depositionflux at QOMS of similar to 10 kg N ha(-1) yr(-1), which is approximately twice the lower value of the critical loadrange reported for the Alpine ecosystem. Such adverse impact is particularlyconcerning, given the anticipated increase of wildfire activitiesin the future under climate change.

The impact of aerosols, especially the absorbing aerosols, in the Himalayan region is important for climate. We closely examine ground-based high-quality observations of aerosol characteristics including radiative forcing from several locations in the Indo-Gangetic Plain (IGP), the Himalayan foothills and the Tibetan Plateau, relatively poorly studied regions with several sensitive ecosystems of global importance, as well as highly vulnerable large populations. This paper presents a state-of-the-art treatment of the warming that arises from these particles, using a combination of new measurements and modeling techniques. This is a first-time analysis of its kind, including ground-based observations, satellite data, and model simulations, which reveals that the aerosol radiative forcing efficiency (ARFE) in the atmosphere is clearly high over the IGP and the Himalayan foothills (80-135 Wm(-2) per unit aerosol optical depth (AOD)), with values being greater at higher elevations. AOD is >0.30 and single scattering albedo (SSA) is similar to 0.90 throughout the year over this region. The mean ARFE is 2-4 times higher here than over other polluted sites in South and East Asia, owing to higher AOD and aerosol absorption (i.e., lower SSA). Further, the observed annual mean aerosol induced atmospheric heating rates (0.5-0.8 Kelvin/day), which are significantly higher than previously reported values for the region, imply that the aerosols alone could account for >50 % of the total warming (aerosols + greenhouse gases) of the lower atmosphere and surface over this region. We demonstrate that the current state-of-the-art models used in climate assessments significantly underestimate aerosol-induced heating, efficiency and warming over the Hindu Kush - Himalaya - Tibetan Plateau (HKHTP) region, indicating a need for a more realistic representation of aerosol properties, especially of black carbon and other aerosols. The significant, regionally coherent aerosol induced warming that we observe in the high altitudes of the region, is a significant factor contributing to increasingair temperature, observed accelerated retreat of the glaciers, and changes in the hydrological cycle and precipitation patterns over this region. Thus, aerosols are heating up the Himalayan climate, and will remain a key factor driving climate change over the region.

The Indo-Gangetic Plain (IGP) is a major regional and global emitter of atmospheric pollutants, which adversely affect surrounding areas such as the Himalayas. We present a comprehensive dataset on carbonaceous aerosol (CA) composition, radiocarbon (D14C) -based source apportionment, and light absorption of total suspended particle (TSP) samples collected over a 3--year period from high-altitude Jomsom in the central Himalayas. The 3-year mean TSP, organic carbon (OC), and elemental carbon (EC) concentrations were 92.0 +/- 28.6, 9.74 +/- 6.31, and 2.02 +/- 1.35 lg m-3, respectively, with the highest concentrations observed during the pre-monsoon season, followed by the post-monsoon, winter, and monsoon seasons. The D14C analysis revealed that the contribution of fossil fuel combustion (ffossil) to EC was 47.9% +/- 11.5%, which is consistent with observations in urban and remote regions in South Asia and attests that EC likely arrives in Jomsom from upwind IGP sources via long-range transport. In addition, the lowest ffossil (38.7% +/- 13.3%) was observed in winter, indicating large contributions in this season from local biomass burning. The mass absorption cross- of EC (MACEC: 8.27 +/- 1.76 m2/g) and watersoluble organic carbon (MACWSOC: 0.98 +/- 0.45 m2/g) were slightly higher and lower than those reported in urban regions, respectively, indicating that CA undergo an aging process. Organic aerosol coating during transport and variation of biomass burning probably led to the seasonal variation in MAC of two components. Overall, WSOC contributed considerably to the light absorption (11.1% +/- 4.23%) of EC. The findings suggest that to protect glaciers of the Himalayas from pollution-related melting, it is essential to mitigate emissions from the IGP.(c) 2022 China University of Geosciences (Beijing) and Peking University. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).

The Tibetan Plateau holds the largest mass of snow and ice outside of the polar regions. The deposition of light-absorbing particles (LAPs) including mineral dust, black carbon and organic carbon and the resulting positive radiative forcing on snow (RFSLAPs) substantially contributes to glacier retreat. Yet how anthropogenic pollutant emissions affect Himalayan RFSLAPs through transboundary transport is currently not well known. The COVID-19 lockdown, resulting in a dramatic decline in human activities, offers a unique test to understand the transboundary mechanisms of RFSLAPs. This study employs multiple satellite data from the moderate resolution imaging spectroradiometer and ozone monitoring instrument, as well as a coupled atmosphere-chemistry-snow model, to reveal the high spatial heterogeneities in anthropogenic emissions-induced RFSLAPs across the Himalaya during the Indian lockdown in 2020. Our results show that the reduced anthropogenic pollutant emissions during the Indian lockdown were responsible for 71.6% of the reduction in RFSLAPs on the Himalaya in April 2020 compared to the same period in 2019. The contributions of the Indian lockdown-induced human emission reduction to the RFSLAPs decrease in the western, central, and eastern Himalayas were 46.8%, 81.1%, and 110.5%, respectively. The reduced RFSLAPs might have led to 27 Mt reduction in ice and snow melt over the Himalaya in April 2020. Our findings allude to the potential for mitigating rapid glacial threats by reducing anthropogenic pollutant emissions from economic activities.

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 C-14-based non-fossil fuel contribution (f(non-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 f(non-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.

Understanding how groundwater storage (GWS) responds to climate change is essential for water resources management and future water availability in the Tibetan Plateau (TP). However, the dominant factor controlling long-term GWS changes remains unclear and its responses to climate change are not well understood. Here we combined multi-source datasets including in-situ measurements, satellite observations, global models, and reanalysis products to reveal that GWS increased at 5.59 +/- 1.44 Gt/yr during 2003-2016 while showing spatial heterogeneities with increasing trends in northern TP and glacial regions and declining trends in central and southern TP. The accelerated transformation from solid water (glaciers, snow, and permafrost; -17.72 +/- 1.53 Gt/yr) into liquid water provide more recharge to groundwater, dominating the total GWS increase. This study contributes to a better understanding of the hydrological cycle under climate change and provides key information for projecting water availability under different future scenarios in the TP.

Downward transport of stratospheric air into the troposphere (identified as stratospheric intrusions) could potentially modify the radiation budget and chemical of the Earth's surface atmosphere. As the highest and largest plateau on earth, the Tibetan Plateau including the Himalayas couples to global climate, and has attracted widespread attention due to rapid warming and cryospheric shrinking. Previous studies recognized strong stratospheric intrusions in the Himalayas but are poorly understood due to limited direct evidences and the complexity of the meteorological dynamics of the third pole. Cosmogenic S-35 is a radioactive isotope predominately produced in the lower stratosphere and has been demonstrated as a sensitive chemical tracer to detect stratospherically sourced air mass in the planetary boundary layer. Here, we report 6-month (April-September 2018) observation of S-35 in atmospheric sulfate aerosols ((SO42-)-S-35) collected from a remote site in the Himalayas to reveal the stratospheric intrusion phenomenon as well as its potential impacts in this region. Throughout the sampling campaign, the (SO42-)-S-35 concentrations show an average of 1,070 +/- 980 atoms/m(3). In springtime, the average is 1,620 +/- 730 atoms/m(3), significantly higher than the global existing data measured so far. The significant enrichments of (SO42-)-S-35 measured in this study verified the hypothesis that the Himalayas is a global hot spot of stratospheric intrusions, especially during the springtime as a consequence of its unique geology and atmospheric couplings. In combined with the ancillary evidences, e.g., oxygen-17 anomaly in sulfate and modeling results, we found that the stratospheric intrusions have a profound impact on the surface ozone concentrations over the study region, and potentially have the ability to constrain how the mechanisms of sulfate oxidation are affected by a change in plateau atmospheric properties and conditions. This study provides new observational constraints on stratospheric intrusions in the Himalayas, which would further provide additional information for a deeper understanding on the environment and climatic changes over the Tibetan Plateau.

South Asian pollutants can be transported and deposited via wet/dry deposition to the remote areas of the Himalayas and could pose a serious threat to the mountain ecosystems. Therefore, in order to understand the concentrations, fluxes, seasonal variation and origin of the mercury (Hg), major ions and trace elements, precipitation samples were collected during 2012-2013 from a data gap region, Jomsom, the high elevation semiarid mountain valley in the central Himalayas. The volume-weighted mean (VWM) concentrations of ions followed the order of Ca2+ > Mg2+ > Na+ > NH4+ > SO42- > Cl- > NO3- > K+. The concentration of Cd was lowest (0.07 mu g L-1) whereas that of Fe was the highest (1073.59 mu g L-1) in the precipitation samples. Wet deposition level of all the measured inorganic species was comparable to urban Lhasa but higher than those in remote alpine sites of the Tibetan Plateau (TP). This study shows that Hg and other inorganic constituents were higher in the non-monsoon season compared to monsoon due to enhanced washout of aerosols. Enrichment factor (EF), sea salt fraction, crustal and anthropogenic fractions, principal component analysis (PCA) and correlation coefficient analysis suggested that crustal dust and anthropogenic activities as the major sources of measured chemical species whereas the influence of sea-salt was minimal. In addition, local anthropogenic emissions were low suggesting that the majority of the pollutants could have been transported from the South Asian region to the high elevation mountains. Meanwhile, low precipitation and dry environment could have enhanced the concentrations of inorganic species in the arid region than other sites over the central Himalayas. This work adds new dataset of inorganic pollutants in wet precipitation and provides baseline information for an arid region environmental protection. However, there is a need for further long-term monitoring to understand the precipitation chemistry of the arid regions.