Dipesh Rupakheti

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.

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.

Assessment of water quality and health risks for toxic trace elements in urban Phewa and remote Gosainkunda lakes, Nepal

ABSTRACT The concentration of 13 metals (Al, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Cd, Pb, and Hg) and their associated health risk assessment was performed for two Himalayan lakes, urban Phewa and remote Gosainkunda, from Nepal. Water Quality Index (WQI), Metal Index (MI), Hazard Quotient (HQ), Hazard Index, and Cancer Risk were calculated in order to evaluate the water quality of these lakes. Correlation analysis revealed that Mn and Fe were derived from natural geological weathering processes and Pb, V, Cr, Co, Ni, Cu, Zn, and Cd might have originated from anthropogenic sources. The results revealed that WQI of the remote lake fell into excellent water quality and urban lake fell into poor water quality, which is also supported by the MI calculation. Moreover, the HQ of Mn in urban lake showed values greater than unity suggesting its health risk to the local inhabitants. The cancer index values indicated “high” risk due to Cr, whereas Cd possesses “very low” cancer risk on local population residing nearby areas. This study provides the useful database and suggests for the regular assessment and policy formulation for safeguarding the natural water bodies in the region.

Long-term trends in the total columns of ozone and its precursor gases derived from satellite measurements during 2004–2015 over three different regions in South Asia: Indo-Gangetic Plain, Himalayas and Tibetan Plateau

ABSTRACT Long-term (2004–2015) satellite data over three adjacent yet contrasting regions: Indo-Gangetic Plain, Himalayas and Tibetan Plateau (TP) were used to study the spatiotemporal distribution of total ozone column (TOC) and its precursor gases (such as nitrogen dioxide (NO2), methane (CH4) and carbon monoxide (CO)). The ozone precursor emission data and forest fire points were used to explore the findings. Trace gases showed increasing trend probably due to increasing emission from South Asia as supported by the Emission Database for Global Atmospheric Research emission data. Strong seasonal variation in trace gases was observed with the highest value during the pre-monsoon season, over three regions, possibly due to the biomass burning, pollution build-up and also long-range transport of pollution. TOC exhibited the similar seasonal variation as shown by the earlier ground-based studies over the region. The total column of precursor gases (except methane) exhibited strong seasonality with the highest column during the pre-monsoon season. Patterns in the variations of TOC and related precursors over the Himalayas were similar with that of the TP. Seasonal climatological trends also exhibited increasing pattern except for CO. This work provides an overview on the long-term TOC and its precursor gases which are necessary to understand the regional climate variability especially over the Himalayas and Tibetan Plateau region.

Concentration and risk assessments of mercury along the elevation gradient in soils of Langtang Himalayas, Nepal

ABSTRACT The fragile Himalayan region could be regarded as the sink for various pollutants transported from urbanized and polluted areas of South Asia. Therefore, in order to understand the concentrations, spatial distribution, pollution, and risk assessments of toxic heavy metal, mercury (Hg), surface soil samples were taken from the central Himalayas in the Langtang region. The average THg concentration in the Langtang Himalayas was 35.75 ± 24.41(ngg−1), which is comparable to the Tibetan top soil values and slightly lower than world average soil values. In addition, an inverse relationship of THg with elevation were observed (i.e. decrease in concentration with increase in elevation) in the Langtang Himalayan soils. Meanwhile, THg concentrations and TOC% were significantly positively correlated at both the depths (0–10 and 10–20 cm), inferring the sorption capacity of organic carbon for Hg. The results of the geo-accumulation index (Igeo), enrichment factor (EF), and pollution index (PI) indicated limited or no pollution by Hg in the Himalayan soils. Further, surface soils had a low potential ecological risk in the region. Therefore, the Hg value from this study could be used for the further evaluation and calculation of Igeo, EF, and PI for water, soil, and aerosol in the Himalayan region as background reference value. However, Hg pollution from long-range transport and atmospheric deposition (wet/dry) in future could not be ignored in the Himalayan region.

Health risk assessment of atmospheric polycyclic aromatic hydrocarbons over the Central Himalayas

ABSTRACT Carcinogenic risk assessments of polycyclic aromatic hydrocarbons (PAHs) in four sites from the Central Himalayas (Bode, Lumbini, Pokhara, and Dhunche) were performed. Lifetime Average Daily Dose (LADD), Lifetime lung cancer risk (LLCR) and Incremental lifetime cancer risk (ILCR) were calculated in order to evaluate the cancer risk. PAHs levels were converted to BaP equivalent concentrations (B[a]Peq), and models of health risk assessment were applied. B[a]Peq concentrations exceeded the standard limited value (1 ng/m3) in all the four sites. The human health risk assessment (HHRA) demonstrated high carcinogenic risk on residents of Bode and Lumbini. Further, LLCR in all sites were over the acceptable range (1.15E-03, 7.90E-04, 1.40E-04 and 9.96E-05, respectively); however, ILCR ranking exhibited acceptable range in Lumbini, Pokhara, and Dhunche (7.10E-06, 1.26E-06, and 8.95E-07). The risk variation among the sites is due to the difference in pollution status. The study shows health risk due to atmospheric PAHs via inhalation prevails all the seasons throughout, differing only seasonally; nevertheless, the concentration and carcinogenic risk decreased remarkably from south-north transect of the central Himalaya. Keeping some uncertainties aside, this study provides noble insights and helps to formulate new advance assessment on the carcinogenic risk of atmospheric PAHs over the Central Himalayas.