Browsing by Author "Gan Zhang"

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Concentrations, sources and health risk of nitrated- and oxygenated-polycyclic aromatic hydrocarbon in urban indoor air and dust from four cities of Nepal
(Elsevier B.V., 2018) Ishwar Chandra Yadav; Ningombam Linthoingambi Devi; Vipin Kumar Singh; Jun Li; Gan Zhang
Although the fate and behavior of parent polycyclic aromatic hydrocarbon (PAHs) have been documented worldwide, the information about PAH-derivatives (NPAHs and OPAHs) is limited, especially in developing countries, including Nepal. Moreover, the greater parts of the investigations concentrating on NPAHs/OPAHs are on the air (borne) particulate phase only; and are primarily based on a limited number of compounds analyzed. Little is known about the environmental concentration, fate, and behavior of NPAHs and OPAHs in air gas phase and dust. In this study, the concentration, fate, spatial distributions of 26 NPAHs and 3 OPAHs in the air (n = 34) and dust (n = 24) were investigated in suspected source area/more densely populated areas of Nepal. Four critical source areas in Nepal were considered as it was conjectured that the urban areas are more prone to NPAH/OPAH contamination due to the high density of automobiles and industrial activities. Overall, the measured ∑19NPAHs in air and dust were 5 and 2 times lower than their parent-PAHs, respectively. Highest levels of NPAHs/OPAHs were measured in Birgunj, followed by Kathmandu, Biratnagar, and Pokhara, respectively, while Biratnagar showed the highest level of ∑OPAHs. 3-Nitrodibenzofuran (3-NDBF) was the most abundant NPAHs measured both in air and dust, whereas 9-Fluorenone (9-FLUONE) prevailing OPAHs. The molecular diagnostic ratio (MDR) of 2-Nitrofluoranthene/1-Nitropyrene indicated the contribution from secondary emission via photochemical reaction as the primary source of NPAHs, while solid fuel combustion and crop residue burning were identified as the essential sources of OPAHs. The human exposure to NPAH/OPAH through the different route of intake suggested dermal contact via dust as the primary pathway of NPAH/OPAH exposure for both adult and children. However, other routes of exposure, for instance, dietary intake or dermal absorption via soil may still be prominent in case of Nepal. © 2018 Elsevier B.V.
Environmental carcinogenic polycyclic aromatic hydrocarbons in soil from Himalayas, India: Implications for spatial distribution, sources apportionment and risk assessment
(Elsevier Ltd, 2016) Ningombam Linthoingambi Devi; Ishwar Chandra Yadav; Qi Shihua; Yang Dan; Gan Zhang; Priyankar Raha
The Indian Himalayan Region (IHR) is one of the important mountain ecosystems among the global mountain system which support wide variety of flora, fauna, human communities and cultural diversities. Surface soil samples (n = 69) collected from IHR were analysed for 16 priority polycyclic aromatic hydrocarbons (PAH) listed by USEPA. The ∑16PAH concentration in surface soil ranged from 15.3 to 4762 ngg-1 (mean 458 ngg-1). The sum total of low molecular weight PAH (∑LMW-PAHs) (mean 74.0 ngg-1) were relatively lower than the high molecular weight PAH (∑HMW-PAHs) (mean 384 ngg-1). The concentration of eight carcinogenic PAHs (BaA, CHR, BbF, BkF, BaP, DahA, IcdP, BghiP) were detected high in mountain soil from IHR and ranged from 0.73 to 2729 ngg-1 (mean 272 ngg-1). Based on spatial distribution map, high concentration of HMW- and LMW-PAHs were detected at GS1 site in Guwahati (615 and 4071 ngg-1), and lowest concentration of HMW-PAHs were found at IS6 in Itanagar (5.80 ngg-1) and LMW-PAHs at DS2 (17.3 ngg-1) in Dibrugarh. Total organic carbon (TOC) in mountain soil was poorly connected with ∑PAHs (r2 = 0.072) and Car-PAHs (r2 = 0.048), suggesting the little role of TOC in adsorption of PAHs. Isomeric ratio of PAHs showed the source of PAH contamination in IHR is mixed of petrogenic and pyrogenic origin and was affirmed by PAHs composition profile. These source apportionment results were further confirmed by principal component analysis (PCA). Eco-toxicological analysis showed the calculated TEQ for most carcinogenic PAH were 2-4 times more than the Dutch allowed limit, while TEQ of BaP was 25 times high, suggesting increasing trend of carcinogenicity of surface soil. © 2015 Elsevier Ltd.
Measurement of legacy and emerging flame retardants in indoor dust from a rural village (Kopawa) in Nepal: Implication for source apportionment and health risk assessment
(Academic Press, 2019) Ishwar Chandra Yadav; Ningombam Linthoingambi Devi; Vipin Kumar Singh; Jun Li; Gan Zhang
Under the Stockholm Convention, signatory countries are obliged to direct source inventories, find current sources, and provide ecological monitoring evidence to guarantee that the encompassing levels of persistent organic pollutants (POPs) are declining. However, such monitoring of different types of POPs are to a great degree constrained in most developing countries including Nepal and are primarily confined to suspected source area/ densely populated regions. In this study, 9 polybrominated diphenyl ethers (PBDEs), 2 dechlorane plus (DPs), 6 novel brominated flame retardants (NBFRs) and 8 organophosphate ester flame retardants (OPFRs) were investigated in indoor dust from a rural area (Kopawa) in Nepal in order to evaluate their occurrence/level, profile, spatial distribution and their sources. Additionally, health risk exposure was estimated to anticipate the possible health risk to the local population. The results showed that OPFRs was the most abundant FR measured in the dust. The concentration of ∑8OPFRs was about 2, 3 and 4 orders of magnitude higher than the ∑6NBFRs, ∑9PBDEs, and ∑2DPs, respectively. Tris (methylphenyl) phosphate (TMPP) and Tris (2-ethylhexyl) phosphate (TEHP) were the most abundant OPFRs analyzed in the dust; while decabromodiphenyl ethane (DBDPE) exceeded among NBFRs. Likewise, 2,2′,3,3′,4,4′,5,5′,6,6′-decabromodiphenylether (BDE-209) was the most identified chemical among PBDEs. The total organic carbon (TOC) content in dust was significantly and positively connected with octa-BDEs (Rho = 0.615, p < 0.01), BTBPE (Rho = 0.733, p < 0.01), TPHP (Rho = 0.621, p < 0.01), TEHP (Rho = 0.560, p < 0.01) and TMPPs (Rho = 0.550, p < 0.01), while black carbon (BC) was either weakly related or not related, suggesting little or no impact of BC in the distribution of FRs. Principal component analysis indicated the contribution from commercial penta-, octa- and deca-BDEs formulation, the adhesive substance, food packaging and paints, and degradation of BDE-209 as the essential sources of FRs. Health risk exposure estimates showed that dermal absorption via dust as the primary route of FRs intake. The estimated daily exposure of PBDEs, NBFRs and OPFRs were 2–10 orders of magnitude lower than their corresponding reference dose (RfD), suggesting insignificant risk. However, other routes such as inhalation and dietary intake might still be significant in the case of Kopawa which should be tested in future. © 2018 Elsevier Inc.
Passive air sampling of organochlorine pesticides in a northeastern state of India, Manipur
(Chinese Academy of Sciences, 2011) Ningombam Linthoingambi Devi; Shihua Qi; Paromita Chakraborty; Gan Zhang; Ishwar Chandra Yadav
Thirty-six polyurethane foam disk passive air samplers (PUF-PAS) were deployed over a year during January to December, 2009 at three locations, i.e., Imphal (urban site), Thoubal (rural site) and Waithou (alpine site) of Manipur, to assess the seasonal local atmospheric emission of selected organochlorine pesticides (OCPs). The average concentration of HCHs monitored at mountain site during hot season (Mar, Apr, and May) and rainy seasons (Jun, Jul, Aug, and Sep) were 403 and 349 pg/m3, respectively. DDTs had a high concentration with 384 pg/m3 at rural site and 379 pg/m3 at urban site during hot seasons. Endosulfans and chlordane were found high in concentration during hot seasons (260 pg/m3) and low during retreating monsoon seasons (44 pg/m3) at rural site. Most of the OCPs concentrations were high during cultivation period. The OCP concentrations of rainy season were highly correlated (p < 0.01) with OCPs of hot seasons. Further, positive correlation (p < 0.05) was also obtained between cold seasons and retreating monsoon. Principal component analysis showed a significant correlation among the four seasons and distribution pattern of OCPs in air. Back trajectory analysis by using HYPSLIT model showed a long range air transport of OCPs to the present study area. Present OCP levels at Manipur is an outcome of both local emission and also movement of air mass by long range atmospheric transport. © 2011 The Research Centre for Eco-Environmental Sciences, Chinese Academy of Sciences.
Selected organochlorine pesticides (OCPs) in surface soils from three major states from the northeastern part of India
(2013) Ningombam Linthoingambi Devi; Paromita Chakraborty; Qi Shihua; Gan Zhang
Eighty-two surface soil samples were collected from forest, grassland, tea estate, wildlife sanctuary, wetland, and roadside areas from the northeastern states of India, viz.; Tripura, Manipur, and Assam. Thirteen different organochlorine pesticides (OCPs) were detected from background soils using gas chromatography electron capture detector. Manipur soils were found to be with higher concentration of dichlorodiphenyltrichloroethanes (DDTs), hexachlorocyclohexanes (HCHs), and endosulfan followed by Tripura and Assam. The spearman correlation coefficient shows significant correlation between HCHs, DDTs, and endosulfan isomers (r 2 > 0.5 and p < 0.05). Additionally, α-HCH, δ-HCH, o,p′-DDE, and endosulfan-sulfate shows good correlation with total organic carbon in soil (r 2 = 0.5, p = 0.05), indicating that the soil organic matter could enhance adsorption of these compounds, also demonstrating that the present OCPs in the background soil were from similar source. Further principal component analysis evaluates that most of the higher volatile compounds where clustered together in soil. However, after comparing with different states of Indian soil samples, the concentrations of OCPs in the present study areas are much lower and comparable with background soil across the globe. © 2013 Springer Science+Business Media Dordrecht.
Spatial distribution, source analysis, and health risk assessment of heavy metals contamination in house dust and surface soil from four major cities of Nepal
(Elsevier Ltd, 2019) Ishwar Chandra Yadav; Ningombam Linthoingambi Devi; Vipin Kumar Singh; Jun Li; Gan Zhang
Raising population, deteriorating environmental conditions and limiting natural resources to handle the key environmental health problems have critically affected human health and the environment. Policy makers and planners in Nepal are more concerned today than at any other time in the past about the deterioration of the environmental condition. Therefore, understanding the connection between pollution and human wellbeing is fundamental endeavors to control pollution exposures and secure human wellbeing. This ability is especially critical for countries like Nepal where the issues of environmental pollution have customarily taken a second place to request for economic development. In this study, spatial distribution and sources of 12 heavy metals (HMs) were investigated in surface soils (n = 24) and house dust (n = 24) from four major urban areas of Nepal in order to mark the pollution level. Additionally, a health risk was estimated to establish the link between HMs pollution and human health. Results showed that the median concentration of Ag, Cd, Co, Cr, Cu, Ni, Pb, Sb, Mn and Zn in soil and dust were 2–13 times greater than the background value. The As, Zn, Cu, Cd, and Pb showed a relatively higher spatial variability in soil and dust. Zn was the most abundant metal measured in dust and soil and accounted for 59% and 55% of ∑7HMs, respectively. The HMs in soil and dust were poorly correlated with total organic carbon (TOC) and black carbon (BC), suggesting little or no influence on HMs contamination. Source analysis study indicated the distribution of Cr, Ni, Sb, Ag, Pb, Cu, and Zn in soil and dust are mainly affected by anthropogenic sources, particularly traffic emissions, industrial source, and domestic households materials, while Co, Fe, As, Mn and Cd were from natural sources. The estimated carcinogenic risk (CR) of HMs in soil and dust exceeded the acceptable level of human exposure, recommending significant CR to the local population. © 2018 Elsevier Ltd