Lekhendra Tripathee

Wet deposition of mercury at Lhasa, the capital city of Tibet

Quantifying the contribution of mercury (Hg) in wet deposition is important for understanding Hg biogeochemical cycling and anthropogenic sources, and verifying atmospheric models. Mercury in wet deposition was measured over the year 2010, in Lhasa the capital and largest city in Tibet. Precipitation samples were analyzed for total Hg (HgT), particulate-bound Hg (HgP), and reactive Hg (HgR). The volume-weighted mean (VWM) concentrations and wet deposition fluxes of HgT, HgP and HgR in precipitation were 24.8 ng L-1 and 8.2 μg m-2 yr-1, 19.9 ng L-1 and 7.1 μg m-2 yr-1, and 0.5 ng L-1 and 0.19 μg m-2 yr-1, respectively. Concentrations of HgT and HgP were statistically higher during the non-monsoon season than during the monsoon season, while HgR concentrations were statistically higher during the monsoon season than during the non-monsoon season. Most HgT, HgP and HgR wet deposition occurred during the monsoon season. Concentrations of HgP and HgR were 77% and 5% of the HgT on average (VWM), respectively. Concentrations of HgT and HgP were weakly negatively correlated with precipitation amount (r2 = 0.09 and 0.10; p < 0.05), indicating that below-cloud scavenging of Hg from the local atmosphere was an important mechanism contributing Hg to precipitation. High HgP%, as well as a significant positive correlation between HgT and HgP, confirms that Hg wet deposition at Lhasa was primarily occurring in the form of atmospheric HgP below-cloud scavenging. Moreover, the HgT concentration, rather than the precipitation amount, was found to be the governing factor affecting HgT wet deposition flux. A comparison among modeled wet and dry deposition fluxes, and measurements suggested that estimates of both wet and dry Hg deposition fluxes by the GEOS-Chem model were 2 to 3 times higher than the measured annual wet flux.

Atmospheric deposition of trace elements recorded in snow from the Mt. Nyainqentanglha region, southern Tibetan Plateau

In May 2009, snowpit samples were collected from a high-elevation glacier in the Mt. Nyainqêntanglha region on the southern Tibetan Plateau. A set of elements (Al, V, Cr, Mn, Co, Ni, Cu, Zn, Cd, Hg and Pb) was analyzed to investigate the concentrations, deposition fluxes of trace elements, and the relative contributions from anthropogenic and natural sources deposited on the southern Tibetan Plateau. Concentrations of most of the trace elements in snowpit samples from the Zhadang glacier are significantly lower than those examined from central Asia (e.g., eastern Tien Shan), with higher concentrations during the non-monsoon season than during the monsoon season. The elements of Al, V, Cr, Mn, Co, and Ni display low crustal enrichment factors (EFs), while Cu, Zn, Cd, Hg, and Pb show high EF values in the snow samples, suggesting anthropogenic inputs are potentially important for these elements in the remote, high-elevation atmosphere on the southern Tibetan Plateau. Together with the fact that the concentration levels of such elements in the Mt. Nyainqêntanglha region are significantly higher than those observed on the south edge of the Tibetan Plateau, our results suggest that the high-elevation atmosphere on the southern Tibetan Plateau may be more sensitive to variations in the anthropogenic emissions of atmospheric trace elements than that in the central Himalayas. Moreover, the major difference between deposition fluxes estimated in our snow samples and those recently measured at Nam Co Station for elements such as Cr and Cu may suggest that atmospheric deposition of some of trace elements reconstructed from snowpits and ice cores could be grossly underestimated on the Tibetan Plateau.

Characterizations of wet mercury deposition on a remote high-elevation site in the southeastern Tibetan Plateau.

Accurate measurements of wet mercury (Hg) deposition are critically important for the assessment of ecological responses to pollutant loading. The Hg in wet deposition was measured over a 3-year period in the southeastern Tibetan Plateau. The volume-weighted mean (VWM) total Hg (HgT) concentration was somewhat lower than those reported in other regions of the Tibetan Plateau, but the VWM methyl-Hg concentration and deposition flux were among the highest globally reported values. The VWM HgT concentration was higher in non-monsoon season than in monsoon season, and wet HgT deposition was dominated by the precipitation amount rather than the scavenging of atmospheric Hg by precipitation. The dominant Hg species in precipitation was mainly in the form of dissolved Hg, which indicates the pivotal role of reactive gaseous Hg within-cloud scavenging to wet Hg deposition. Moreover, an increasing trend in precipitation Hg concentrations was synchronous with the recent economic development in South Asia.

Spatial distribution, sources and risk assessment of potentially toxic trace elements and rare earth elements in soils of the Langtang Himalaya, Nepal

Soils in the fragile Himalayan region could be affected by the transport and deposition of potentially toxic trace metals (PTEs) from urban and industrialized areas of South Asia. The transported pollutants could pose a serious threat to the soil quality in the pristine regions at high elevations having minimal direct human influence. Therefore, it is important to understand the geochemical and physical characteristics of soils in this region and determine the extent of their chemical pollution. In order to achieve these objectives, soil samples were collected from different elevation transects of the Langtang Himalaya in Nepal. The samples were analyzed for PTEs and rare earth elements for the purpose of identifying their possible sources and to evaluate their environmental risk in the region. The PTEs and REEs concentrations were measured by ICP-MS (X-7; Thermo-elemental, USA) and total organic carbon (TOC) by TOC analyzer. The results of this study were comparable to those of the world average background soil as well as the Tibetan plateau surface soil. TOC revealed a decreasing trend with increasing elevation. Correlation analysis and principle component analysis (PCA) indicated that most of the elements were highly associated with major crustal elements, suggesting that their primary sources were of natural origin. Furthermore, the geo-accumulation index (Igeo), enrichment factor (EF) and pollution index (PI) analyses indicated that the Himalayan soils represent minimal pollution and the data from this study may be used as background values for the Himalayan region in the future studies. REEs in the soil samples were found to be consistent with an order of average abundance of the Earth’s crust. In addition, the chondrite-normalized REE distribution of the light REE suggested enrichment of LREE and Eu depletion. Moreover, this study emphasized that soils of the Himalayan region could, in future, be under threat of elemental pollution from long-range transport via atmospheric circulation and deposition.

Distribution and transportation of mercury from glacier to lake in the Qiangyong Glacier Basin, southern Tibetan Plateau, China.

The Tibetan Plateau is home to the largest aggregate of glaciers outside the Polar Regions and is a source of fresh water to 1.4 billion people. Yet little is known about the transportation and cycling of Hg in high-elevation glacier basins on Tibetan Plateau. In this study, surface snow, glacier melting stream water and lake water samples were collected from the Qiangyong Glacier Basin. The spatiotemporal distribution and transportation of Hg from glacier to lake were investigated. Significant diurnal variations of dissolved Hg (DHg) concentrations were observed in the river water, with low concentrations in the morning (8:00am-14:00pm) and high concentrations in the afternoon (16:00pm-20:00pm). The DHg concentrations were exponentially correlated with runoff, which indicated that runoff was the dominant factor affecting DHg concentrations in the river water. Moreover, significant decreases of Hg were observed during transportation from glacier to lake. DHg adsorption onto particulates followed by the sedimentation of particulate-bound Hg (PHg) could be possible as an important Hg removal mechanism during the transportation process. Significant decreases in Hg concentrations were observed downstream of Xiao Qiangyong Lake, which indicated that the high-elevation lake system could significantly affect the distribution and transportation of Hg in the Qiangyong Glacier Basin.

Mercury and Selected Trace Elements from a Remote (Gosainkunda) and an Urban (Phewa) Lake Waters of Nepal

Two lakes, one from the remote high altitude on the southern slope of the Himalaya (Lake Gosainkunda) and another from the urban mid-hill area (Lake Phewa) were studied for evaluating anthropogenic inputs of the pollutants, particularly mercury (Hg) and other trace elements (TEs) (such as Al, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd, and Pb). A total of 77 water samples, 24 from Lake Gosainkunda and 53 from Lake Phewa were collected from different depth profiles during October/November 2010. Concentrations of Hg were significantly higher in Lake Gosainkunda compared to Lake Phewa probably due to long-range transport of Hg and its deposition on high altitudes of the Himalayas, in addition to the probable natural geological sources. Some of the TEs (such as Al, V, Cr, Mn, Fe, and Co) show crustal origin in Lake Gosainkunda, whereas others such as Ni, Cu, Zn, Cd, and Pb indicate possible anthropogenic origin (enrichment factor (EF) > 4). On the other hand, Al, V, Cr, Ni, and Cu show crustal origin in Lake Phewa and the remaining TEs (Mn, Fe, Co, Zn, Cd, and Pb) showed high EF values relative to the crustal elements suggesting potential anthropogenic inputs of the pollutants. The study further indicates that two studied lakes have different potential sources for Mn, Fe, Co, Ni, and Cu regarding TE pollution. A high enrichment of Cd and Pb in high-altitude lake (with less anthropogenic activities) compared to the low-altitude lake (with high anthropogenic activities) indicates atmospheric long-range transportation of the pollutants in remote areas of the Himalayas which might be possible as air masses pass through the industrial areas and deposit in the high altitudes.

Trace elements and rare earth elements in wet deposition of Lijiang, Mt. Yulong region, southeastern edge of the Tibetan Plateau

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.

Influence of long-range transboundary transport on atmospheric water vapor mercury collected at the largest city of Tibet.

Monsoon circulation is an important process that affects long-range transboundary transport of anthropogenic contaminants such as mercury (Hg). During the Indian monsoon season of 2013, a total of 92 and 26 atmospheric water vapor samples were collected at Lhasa, the largest city of the Tibet, for Hg and major ions analysis, respectively. The relatively low pH/high electronic conductivity values, together with the fact that NH4(+) in atmospheric water vapor was even higher than that determined in precipitation of Lhasa, indicated the effects of anthropogenic perturbations through long-range transboundary atmospheric transport. Concentrations of Hg in atmospheric water vapor ranged from 2.5 to 73.7ngL(-1), with an average of 12.5ngL(-1). The elevated Hg and major ions concentrations, and electronic conductivity values were generally associated with weak acidic samples, and Hg mainly loaded with anthropogenic ions such as NH4(+). The results of principal component analysis and trajectory analysis suggested that anthropogenic emissions from the Indian subcontinent may have largely contributed to the determined Hg in atmospheric water vapor. Furthermore, our study reconfirmed that below-cloud scavenging contribution was significant for precipitation Hg in Lhasa, and evaluated that on average 74.1% of the Hg in precipitation could be accounted for by below-cloud scavenging.

Variations of the Physicochemical Parameters and Metal Levels and Their Risk Assessment in Urbanized Bagmati River, Kathmandu, Nepal

During post-monsoon 2013, surface water samples were collected form 34 sites from the Bagmati River and its tributaries within the Kathmandu Valley to assess the river water quality. The physical parameters were measured on site and major ions (Na

Characterizations of atmospheric particulate-bound mercury in the Kathmandu Valley of Nepal, South Asia

The Kathmandu Valley, located in the Himalayan foothills in Nepal, is heavily polluted. In order to investigate ambient particulate-bound mercury (Hg) in the Kathmandu Valley, a total 64 total suspended particulates (TSP) samples were collected from a sub-urban site in the Kathmandu Valley, the capital region of Nepal during a sampling period of an entire year (April 2013-April 2014). They were analyzed for ambient particulate-bound Hg (PBM) using thermal desorption combined with cold vapor atomic spectroscopy. In our knowledge, it is the first study of ambient PMB in the Kathmandu Valley and the surrounding broader Himalayan foothill region. The average concentration of PBM over the entire sampling period of a year was found to be 850.5 (±962.8) pg m-3 in the Kathmandu Valley. This is comparable to those values reported in the polluted cities of China and significantly higher than those observed in most of urban areas in Asia and other regions of world. The daily average Hg contents in TSP (PBM/TSP) ranges from 269.7 to 7613.0ngg-1 with an average of 2586.0 (±2072.1) ng g-1, indicating the high enrichment of Hg in TSP. The average concentrations of PBM were higher in the winter and pre-monsoon season than in the monsoon and post-monsoon season. The temporal variations in the strength of anthropogenic emission sources combined with other influencing factors, such as ambient temperature and the removal of atmospheric aerosols by wet scavenging are attributable to the seasonal variations of PBM. The considerably high dry deposition flux of PBM estimated by using a theoretical model was 135μgm-2yr-1 at the Kathmandu Valley. This calls for an immediate attention to addressing ambient particulate Hg in the Kathmandu Valley, including considering it as a key component of future air quality monitoring activities and mitigation measures.