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 mu eq/L; SO42- : 1.73 mu eq/L) were significantly higher than those at a site around 2.2 Km away ( Ca2+: 11.47 mu eq/L; SO42- : 0.64 mu eq/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.

Mt. Everest (Qomolangma or Sagarmatha), the highest mount on Earth and located in the central Himalayas between China and Nepal, is characterized by highly concentrated glaciers and diverse landscapes, and is considered to be one of the most sensitive area to climate change. In this paper, we comprehensively synthesized the climate and environmental changes in the Mt. Everest region, including changes in air temperature, precipitation, glaciers and glacial lakes, atmospheric environment, river and lake water quality, and vegetation phenology. Historical temperature reconstruction from ice cores and tree rings revealed the distinct features of 20th century warming in the Mt. Everest region. Meteorological observations further proved that the Mt. Everest region has been experiencing significant warming (approximately 0.33 degrees C/decade) but relatively stable precipitation during 1961-2018 AD. Projected results (during 2006-2099 AD) under different representative concentration pathway scenarios showed a general warming trend in the region, with larger warming occurring in winter than in summer. Meanwhile, the precipitation projections varied spatially with no significant trends over the region. Intensive glacier shrinkage was characterized by decreasing glacier areas, while glacier-fed river runoff increased. Glacial lakes expanded with increasing glacial lake areas and numbers. These findings indicated a clear regional hydrological response to climate warming. Owing to the remote location of Mt. Everest, the present atmospheric environment remained relatively clean; however, long-range transport of atmospheric pollutants from South Asia and West Asia may have substantially influenced the Mt. Everest region, resulting in increasing concentrations of pollutants since the Industrial Revolution. Anthropogenic activities have been shown to influence river and lake water quality in this remote region, especially in the downstream. The end of the vegetation growing season advanced in the northern slope and did not change in southern slope region of the Mt. Everest, and there was no significant change in start date of the growing season in the region. This review will enhance our understanding of climate and environmental changes in the Mt. Everest region under global warming.

Short-lived climate pollutants (SLCPs) including methane, tropospheric ozone, and black carbon in this work, is a set of compounds with shorter lifetimes than carbon dioxide (CO2) and can cause warming effect on climate. Here, the effective radiative forcing (ERF) is estimated by using an online aerosol-climate model (BCC_AGCM2.0_CUACE/Aero); then the climate responses to SLCPs concentration changes from the pre-industrial era to the present (1850-2010) are estimated. The global annual mean ERF of SLCPs was estimated to be 0.99 [0.79-1.20] W m(-2), and led to warming effects over most parts of the globe, with the warming center (about 1.0 K increase) being located in the mid-high latitudes of the Northern Hemisphere (NH) and the ocean around Antarctica. The changes in annual mean surface air temperature (SAT) caused by SLCPs changes were more prominent in the NH [0.78 (0.62-0.94) K] than in the Southern Hemisphere [0.62 (0.45-0.74) K], and the global annual mean value is 0.70 K. By looking at other variable responses, we found that precipitation had been increased by about 0.10 mm d(-1) in mid- and high-latitudes and decreased by about 0.20 mm d(-1) in subtropical regions, with the global annual mean value of 0.02 mm d(-1). Changes in SLCPs also influenced atmospheric circulation change, a northward shift in the Intertropical Convergence Zone was induced due to the interhemispheric asymmetry in SAT. However, it is found in this work that SLCPs changes had little effect on global average cloud cover, whereas the local cloud cover changes could not be ignored, low cloud cover increase by about 2.5% over high latitudes in the NH and the ribbon area near 60 degrees S, and high cloud cover increased by more than 2.0% over northern Africa and the Indian Ocean. Finally, we compared the ERFs and global and regional warming effects of SLCPs with those induced by CO2 changes. From 1850 to the present, the ERF of SLCPs was equivalent to 66%, 83%, and 50% of that of CO2 in global, NH, and SH mean, respectively. The increases in SAT caused by SLCPs were 43% and 55% of those by CO2 over the globe and China, respectively.

The unprecedented COVID-19 outbreak impacted the world in many aspects. Air pollutants were largely reduced in cities worldwide in 2020. Using samples from two snow pits dug separately in 2019 and 2020 in Urumqi Glacier No. 1 (UG1) in the Xinjiang Uygur Autonomous Region (Xinjiang), China, we measured water-stable isotopes, soluble ions, and black and organic carbon (BC and OC). Both carbon types show no significant variations in the snow-pit profiles dated from 2018 through 2020. The deposition of anthropogenically induced soluble ions (K+, Cl-, SO42-, and NO3-) in the snow decreased to 20-40% of their respective concentrations between 2019 and 2020; however, they increased 2- to fourfold from 2018 to 2019. We studied the daily concentrations of SO2 (2019-2020), NO2 (2015-2020), CO (2019-2020), and PM2.5 (2019-2020) measured in the sixteen major cities and towns across Xinjiang. The variabilities in these air pollutants were supposed to illustrate the air quality in the urban area and represent the change in the source area. The NO2 decreased in response to mobility restrictions imposed by local governments, while SO2, CO, and PM2.5 did not consistently correspond. This difference indicates that the restriction measures primarily affected traffic. The increases in chemical species in the snow from 2018 to 2019 and the subsequent decreases from 2019 to 2020 were consistent with the variations in SO2 and NO2 measured in urban air and estimated by MERRA-2 model. Therefore, the pandemic could possibly have an impact on snow chemistry of the Tien-Shan glaciers via reduced traffic and industrial intensity; more evidence would be obtained from ice cores, tree rings, and other archives in the future.

Air pollution is a grand challenge of our time due to its multitude of adverse impacts on environment and society, with the scale of impacts more severe in developing countries, including China. Thus, China has initiated and implemented strict air pollution control measures over last several years to reduce impacts of air pollution. Monitoring data from Jan 2015 to Dec 2019 on six criteria air pollutants (SO2, NO2, CO, O-3, PM2.5, and PM10) at eight sites in southwestern China were investigated to understand the situation and analyze the impacts of transboundary air pollutants in this region. In terms of seasonal variation, the maximum concentrations of air pollutants at these sites were observed in winter or spring season depending on individual site. For diurnal variation, surface ozone peaked in the afternoon while the other pollutants had a bimodal pattern with peaks in the morning and late afternoon. There was limited transport of domestic emissions of air pollutants in China to these sites. Local emissions enhanced the concentrations of air pollutants during some pollution events. Mostly, the transboundary transport of air pollution from South Asia and Southeast Asia was associated with high concentrations of most air pollutants observed in southwestern China. Since air pollutants can be transported to southwestern China over long distances from the source regions, it is necessary to conduct more research to properly attribute and quantify transboundary transport of air pollutants, which will provide more solid scientific guidance for air pollution management in southwestern China. (C) 2021 China University of Geosciences (Beijing) and Peking University. Production and hosting by Elsevier B.V.

The study focusses to investigate the variations in aerosol characteristics, concentrations and radiative properties due to the burning of firecrackers during Diwali festival event followed with New year festival celebrations over a representative urban environment. A six day's long intensive in situ measurements of Black Carbon, Particulate Matter and Aerosol Optical Depth were collected to capture pre to post-Diwali and New Year festival celebrations marked with massive fireworks. We observed an increase of 286%, 89.5%, and 60.5%, in BC, PM10, and PM2.5 concentrations, respectively on festival night as compared to pre-event days. An increase in in situ measured AOD is comparable with concurrent satellite derived AOD. Angstrom exponent, alpha > 1.0 along with high turbidity coefficient; beta estimated for the festival period clearly implies the abundance of fine-mode particles, probably the smoke aerosols loading from fireworks. The Mie-scattered return signals received by the ground based Raman LiDAR at 532 nm showed an increased concentration of 'anthropogenic aerosols', attributed to the increased crackers activity. Space based CALIPSO LiDAR observations also validate the presence of 'polluted dust' and 'smoke' types aerosols at the near surface to 5 km altitude over the study area. A sharp increase in gaseous air pollutants like SO2 and NOx concentrations exceeding the National Ambient Air Quality Standards is also observed. The COART model run simulations in SWIR region showed an increased 'cooling' at the surface (-125 Wm(-2) to -185 Wm(-2)) as compared to 'warming' in the atmosphere during the event period. A maximum heating rate (1.9 Kday(-1)) due to total aerosol radiative forcing is also estimated. These investigations provide useful insights into the impact of burning firecrackers on urban air quality besides radiative impacts at a regional scale. Such celebration induced air pollution events may lead to severe health impacts; particularly respiratory and cardiovascular ailments in the resident population.

Short-lived climate pollutants (SLCPs) including black carbon (BC), methane (CH4), and tropospheric ozone (O-3) are major climate forcers after carbon dioxide (CO2). These SLCPs also have detrimental impacts on human health and agriculture. Studies show that the Hindu Kush Himalayan (HKH) region, which includes Nepal, has been experiencing the impacts of these pollutants in addition to greenhouse gases. In this study, we derive a national-level emission inventory for SLCPs, CO2, and air pollutants for Nepal and project their impacts under reference (REF) and mitigation policy (POL) scenarios. The impacts on human health, agriculture, and climate were then estimated by applying the following: (1) adjoint coefficients from the Goddard Earth Observing System (GEOS)-chemical transport model that quantify the sensitivity of fine particulate matter (PM2.5) and surface O-3 concentrations in Nepal, and radiative forcing in four latitudinal bands, to emissions in 2 x 2.5 degrees grids, and (2) concentration-response functions to estimate health and crop loss impacts in Nepal. With the mitigating measures undertaken, emission reductions of about 78% each of BC and CH4 and 87% of PM2.5 could be achieved in 2050 compared with the REF scenario. This would lead to an estimated avoidance of 29,000 lives lost and 1.7 million tonnes of crop loss while bringing an economic benefit in present value of 2.7 times more than the total cost incurred in its implementation during the whole period 2010-2050. The results provide useful policy insights and pathways for evidence-based decision-making in the design and effective implementation of SLCP mitigation measures in Nepal.

Snowpack and glacial melt samples were collected to understand the hydrochemical, isotopic characteristics and the source of Hg contamination in high altitude glacierized Himalayan catchment. Both the snow and glacial melt were acidic in nature with calcium and magnesium as the dominant cations and bicarbonate and chloride as the dominant anions. The major ion concentrations for cations were found to be Ca2+>Mg2+>Na+>K+ and HCO3->Cl->SO42->NO3- for anions. The atmospheric processes like the precipitation source and aerosol scavenging control the snow chemistry and the weathering of the rocks modify the hydrochemistry of glacial melt. The samples of both the snow and glacial melt were classified as Ca-Mg-HCO3- type. The concentration of Hg in snow (154.95ngL(-1)) and glacial melt (112.04ngL(-1)) was highest (still lower compared to the maximum permissible limit (1000ngL(-1)) by WHO in drinking water) during summer season (August-September) and lowest (snow 2.2 and 40.01ngL(-1) for glacial melt) during winter (November). The results reveal that mercury concentration in snowpacks is attributed to the combined mixing of long-range transport of pollutants via westerlies throughout the year and the industrial effluents coming from highly industrial belts of Panjab, Haryana, Rajasthan, Indo-Gangetic plains, and neighboring areas via southwest monsoons during August-September. However, in glacial melt, the Hg concentration was typically controlled by rate of melting, leaching, and percolation. Higher degree and rate of glacial melting decreases the Hg concentration in glacial melt. Stable isotopic analysis and backward air mass trajectory modeling also corroborate the source of precipitation from southwest monsoons during August-September, with its air mass trajectories passing through the highly industrialized belts of Indo-Gangetic plain and adjoining areas.

The Tibetan Plateau is the largest high altitude landform on Earth, with an area of over 2.5x10(6) km(2) and an average elevation of similar to 4000 m above sea level. With a unique multisphere environmental system, the Tibetan Plateau provides an important ecological sheltering function for China and other parts of Asia. The Tibetan Plateau is one of the world's most pristine regions, benefiting from a sparse population with negligible local influence on its environment. However, it is surrounded by some of the most polluted areas in the world, such as South Asia, East Asia, and Southeast Asia. With the atmospheric circulation, such pollutants may impact the Tibetan Plateau through long-range transport. Clearly, the scientific research on the transboundary transport of pollutants is not only important for the understanding of multisphere interactions on the earth surface, but also could meet the national strategic needs for ecological and environmental protection. Long-term monitoring combined with short-term intensive observation campaigns, were used to comprehensively summarize the latest research progress regarding the spatial-temporal distribution and transport mechanism of air pollutants, as well as their climate and ecological impacts, which were achieved during the Second Tibetan Plateau Scientific Expedition. With respect of historical trends reconstructed from environmental archives, e.g., glacial ice cores and lake sediments, the black carbon and heavy metals like mercury show a dramatic increase since 1950s, which reflect the enhanced emission of air pollutants in Asia. On-line observation data and WRF-Chem modeling indicate that upper air circulation and local mountain-valley breeze system are the main drivers of trans Himalaya air pollution from South Asia. A regional climate-chemistry model coupled with an aerosol-snow/ice feedback module was used to reveal the natural and anthropogenic light-absorbing aerosols' radiative effects over the Tibetan Plateau. Results indicated that the mineral dust both in the atmosphere and snow induced 0.1-0.5 degrees C warming over the western Tibetan Plateau and Kunlun Mountains in spring. Meanwhile, dust aerosols caused snow water equivalent to decrease by 5-25 mm over the western TP, Himalayas and Pamir Mountains in winter and spring. The radiative effects of BC-in-snow induced surface temperature increased by 0.1-1.5 degrees C and snow water equivalent decreased by 5-25 mm over the western Tibetan Plateau and Himalayas. According to the observations the black carbon and dust found in the snow and ice on the surfaces of glaciers were responsible for on average 20% of the albedo reduction within the TP region. Those atmospherically transported pollutants also have obvious negative impacts on the ecosystem in Tibetan Plateau. For example, bioaccumulation of DDTs have been found in Tibetan terrestrial and aquatic food chains, and newly emerging compounds such as polyfluoroalkyl substances and hexabromocyclodo-decanes have been widely detected in wild fish species. Therefore, the corresponding ecological risks are of great concern. In the future, it is necessary to quantify the extent of atmospherically transported pollution and model the pollutant fate under the future environmental scenarios as well as establish environmental and health risk.

We used an online aerosol-climate model (BCC_AGCM2.0_CUACE/Aero) to simulate effective radiative forcing and climate response to changes in the concentrations of short-lived climatic pollutants (SLCPs), including methane, tropospheric ozone, and black carbon, for the period 2010-2050 under Representative Concentration Pathway scenarios (RCPs) 8.5, 4.5, and 2.6. Under these three scenarios, the global annual mean effective radiative forcing were 0.1, -0.3, and -0.5Wm(-2), respectively. Under RCP 8.5, the change in SLCPs caused significant increases in surface air temperature (SAT) in middle and high latitudes of the Northern Hemisphere and significant decreases in precipitation in the Indian Peninsula and equatorial Pacific. Global mean SAT and precipitation increased by 0.13K and 0.02 mmd(-1), respectively. The reduction in SLCPs from 2010 to 2050 under RCPs 4.5 and 2.6 led to significant decreases in SAT at high latitudes in the Northern Hemisphere. Precipitation increased slightly in most continental regions, and the Intertropical Convergence Zone moved southward under both of these mitigation scenarios. Global mean SAT decreased by 0.20 and 0.44K, and global averaged precipitation decreased by 0.02 and 0.03 mmd(-1) under RCPs 4.5 and 2.6, respectively.