The rapid growth of the production of electrical and electronic products has meant an equally rapid growth in the amount of electronic waste (e-waste), much of which is illegally imported to India, for disposal presenting a serious environmental challenge. The environmental impact during e-waste recycling was investigated and metal as well as other pollutants [e.g. polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs)] were found in excessive levels in soil, water and other habitats. The most e-waste is dealt with as general or crudely often by open burning, acid baths, with recovery of only a few materials of value. As resulted of these process; dioxins, furans, and heavy metals are released and harmful to the surrounding environment, engaged workers, and also residents inhabiting near the sites. The informal e-waste sectors are growing rapidly in the developing countries over than in the developed countries because of cheapest labor cost and week legislations systems. It has been confirmed that contaminates are moving through the food chain via root plant translocation system, to the human body thereby threatening human health. We have suggested some possible solution toward in which plants and microbes combine to remediate highly contaminated sites.

We utilize the distribution of PM2.5 concentration and population in large cities at the global scale to illustrate the relationship between urbanization and urban air quality. We found: 1) The relationship varies greatly among continents and countries. Large cities in North America, Europe, and Latin America have better air quality than those in other continents, while those in China and India have the worst air quality. 2) The relationships between urban population size and PM2.5 concentration in large cities of different continents or countries were different. PM2.5 concentration in large cities in North America, Europe, and Latin America showed little fluctuation or a small increasing trend, but those in Africa and India represent a “U” type relationship and in China represent an inverse “U” type relationship. 3) The potential contribution of population to PM2.5 concentration was higher in the large cities in China and India, but lower in other large cities.

Size-segregated aerosol samples were collected in New Delhi, India from March 6 to April 6, 2012. Homologous series of n-alkanes (C19C33), n-fatty acids (C12C30) and n-alcohols (C16C32) were measured using gas chromatography/mass spectrometry. Results showed a high-variation in the concentrations and size distributions of these chemicals during non-haze, haze, and dust storm days. In general, n-alkanes, n-fatty acids and n-alcohols presented a bimodal distribution, peaking at 0.7–1.1 μm and 4.7–5.8 μm for fine modes and coarse modes, respectively. Overall, the particulate matter mainly existed in the coarse mode (≥2.1 μm), accounting for 64.8–68.5% of total aerosol mass. During the haze period, large-scale biomass burning emitted substantial fine hydrophilic smoke particles into the atmosphere, which leads to relatively larger GMDs (geometric mean diameter) of n-alkanes in the fine mode than those during the dust storms and non-haze periods. Additionally, the springtime dust storms transported a large quantity of coarse particles from surrounding or local areas into the atmosphere, enhancing organic aerosol concentration and inducing a remarkable size shift towards the coarse mode, which are consistent with the larger GMDs of most organic compounds especially in total and coarse modes. Our results suggest that fossil fuel combustion (e.g., vehicular and industrial exhaust), biomass burning, residential cooking, and microbial activities could be the major sources of lipid compounds in the urban atmosphere in New Delhi.

An elaborate survey on the contamination of heavy metals was carried out in surface sediments of different ecosystems such as Vellar-Coleroon estuarine, Pichavaram mangrove and coastal region of Parangipettai, Southeast coast of India. The study was intended since, the coal based thermal power plant and oil refinery plant are proposed to set up along this coast and aquaculture industries and dredging activities are developing. The parameters such as soil texture, pH, total organic carbon (TOC) and heavy metal (Fe, Mn, Cu, Cd, Zn and Ni) concentrations were analyzed for the surface sediments during pre and postmonsoon seasons. Among the metals analyzed, Fe and Mn were found to have dominant as the levels were recorded as 11,804 μg g−1 and 845.2 μg g−1 respectively. A significant correlation was observed between total organic carbon (TOC) and heavy metals. In the mangrove ecosystem, the levels of heavy metals found to be maximum indicating that the rich organic matter acts as an efficient binding agent for metals. The overall finding of the present study indicated that the sediments from the entire Vellar-Coleroon estuarine and Pichavaram mangrove ecosystems were found moderately polluted with cadmium metal. The result of cluster analysis indicated disparity in accumulation of heavy metals in sediments of different ecosystems due to the variations in organic matter. The heavy metals were transported from land to coastal through flood during monsoon season reflecting the variations in their levels in different ecosystems at postmonsoon season.

Urbanization of coastal areas in recent years has driven us to consider a new approach for visually delineating sites that are contaminated with fecal bacteria (FB) in the coastal waters of the Andaman Islands in India. Geo-spatial analysis demarcated harbor, settlement, and freshwater/discharge influenced zones as hot spots for FB, while the open sea was demarcated as a cold spot. The land use types, such as developed and agriculture, with more anthropogenic activities increasing the FB counts while open sea showed the least FB. Box whisker plot indicated an increasing FB trend in the coastal waters during monsoon. Furthermore, principal component analysis revealed 67.35%, 78.62% and 70.43% of total variance at Port Blair, Rangat and Aerial bays, respectively. Strong factor loading was observed for depth (0.95), transparency (0.93), dissolved oxygen (0.93) and fecal streptococci (0.85). Distance proximity analysis revealed that fecal contaminations diluted significantly (P < 0.05) at the distance of 2.1 km toward the deeper or open sea water. This study demonstrates the effectiveness of an integrated approach in identifying the sources of fecal contamination and thus helping in better monitoring and management of coastal waters.

The concentration, distribution and ecological risk of polycyclic aromatic hydrocarbons (PAHs) have been investigated in surface sediments near Bhavnagar coast. The concentration of ∑PAHs ranged from 5.02 to 981.18 μg g−1 dry weight, indicating heavy pollution compared to other historically polluted study sites. It was found to be introduced via mixed origins such as burning of gas, oil, coal, production of petrochemicals, cement, and rubber tires. Domestic fuel burning and motor vehicles are also culprits for air pollution. Industrial effluents and accidental oil spillage can also be considered. PAHs can be exposed through air, water, soil and food sources including ingestion, inhalation, and dermal content in both occupational and non-occupational levels by single or sometimes multiple exposures routes concomitantly. Furthermore, diagnostic ratios, statistical principal component analysis (PCA) and hierarchical cluster analysis (HCA) models have confirmed that the sources of PAHs were both - petrogenic and pyrogenic. For both the sites, assessment of ecological risk of the elevated levels of these pollutants has been exercised based on toxic equivalency factors (TEFs) and risk quotient (RQ) methods. The composite results indicated accurately that both the sites, bears potentially acute and chronic health hazards such as decreased immune functionality, genotoxicity, malignancy and developmental malfunctions in humans. The sites studied here and the workers have been exposed to hazardous pollutants for a longer period of time. Evidences indicate that mixtures of PAHs are carcinogenic to humans, based on occupational studies on workers, exposed to these pollutants. Hence, the present study and statistical approaches applied herein clearly indicate the historic mix routes of PAHs that resulted in magnified concentrations leading to high ecosystem risk. Thus, the scientific communities are urged to develop strategies to minimize the concentrations of PAHs from the historically impacted coastlines, thereby concerning for the future investigations and restoration of these sites.

Many perfluoroalkyl substances (PFAS) are ubiquitous environmental contaminants. They have been widely used in production processes and daily-use products or may result from degradation of precursor compounds in products or the environment. India, with its developing industrialization and population moving from traditional to contemporary lifestyles, represents an interesting case study to investigate PFAS emission and exposure along steep environmental and socioeconomic gradients. This study assesses PFAS concentrations in river and groundwater (used in this region as drinking water) from several locations along the Ganges River and estimates direct emissions, specifically for PFOS and PFOA. 15 PFAS were frequently detected in the river with the highest concentrations observed for PFHxA (0.4–4.7 ng L⁻¹) and PFBS (<MQL – 10.2 ng L⁻¹) among PFCAs and PFSAs, respectively. Prevalence of short-chain PFAS indicates that the effects of PFOA and PFOS substitution are visible in environmental samples from India. The spatial pattern of C5–C7 PFCAs co-varied with that of PFOS suggesting similar emission drivers. PFDA and PFNA had much lower concentrations and covaried with PFOA especially in two hotspots downstream of Kanpur and Patna. PFOS and PFOA emissions to the river varied dramatically along the transect (0.20–190 and 0.03–150 g d⁻¹, respectively). PFOS emission pattern could be explained by the number of urban residents in the subcatchment (rather than total population). Per-capita emissions were lower than in many developed countries. In groundwater, PFBA (<MQL – 9.2 ng L⁻¹) and PFBS (<MQL – 4.9 ng L⁻¹) had the highest concentrations among PFCAs and PFSAs, respectively. Concentrations and trends in groundwater were generally similar to those observed in surface water suggesting the aquifer was contaminated by wastewater receiving river water. Daily PFAS exposure intakes through drinking water were below safety thresholds for oral non-cancer risk in all age groups.

Size-segregated particulate pollutants (PM<0.95, PM0.95–1.5, PM1.5–3.0, PM3.0–7.2 and PM>7.2) were collected over Patiala (30.33°N, 76.40°E; 250 m amsl), a semi-urban city located in northwestern Indo-Gangetic Plain (IGP), during October, 2012 to September, 2013. Mass concentration of total suspended particulates (TSP), derived by summation of particulate (aerosol) mass in different size range, varied from 88 to 387 μg m−3 with highest mass concentration (∼55% of total mass) in submicron size (PM<0.95) during the entire study period, which broadly reflects relative higher contribution of various anthropogenic sources (emissions from biomass and bio-fuel burning, vehicles, thermal power plants, etc) to ambient particles. Concentration of SO42−, NO3−, NH4+, K+ and Ca2+ exhibited large variability ranging from 0.52 to 40, 0.20 to 19, 0.14 to 12, 0.06 to 5.3 and 0.08 to 5.6 μg m−3, respectively, in different size ranges with varying size distribution for most of the species, except NH4+. A strong linear correlation (r = 0.97) between (SO42− + NO3−) and (K+ + NH4+) concentrations has been observed in submicron particles collected in different seasons, suggesting the formation of secondary inorganic salts. However, relatively poor correlation is observed in higher size ranges where significant correlation between (SO42− + NO3−) and (Ca2+ + Mg2+) has been observed. These observations indicate the acid neutralization by dust in coarser modes of particles. Chemical composition of submicron particulates (PM<0.95) in different seasons as well as for whole year was used to identify PM sources through the application of Positive Matrix Factorization (PMF, version 5.0) model. Based on annual data, PMF analyses suggests that six source factors namely biomass burning emission (24%), vehicular emission (22%), secondary organic aerosols (20%), power plant emission (13%), secondary inorganic aerosols (12%) and mineral dust (9%) contribute to PM<0.95 loading over the study region. Such studies are important in dispersion modeling, health impact assessment, and planning of pollution mitigation strategies.

Bacterial degradation of crude oil in response to nutrient treatments has been vastly studied. But there is a paucity of information on kinetic parameters of crude oil degradation. Here we report the nutrient stimulated kinetic parameters of crude oil degradation assessed in terms of CO2 production and oil removal by Pseudomonas aeruginosa AKS1 and Bacillus sp. AKS2. The hydrocarbon degradation rate of P. aeruginosa AKS1 in oil only amended sediment was 10.75 ± 0.65 μg CO2-C g−1 sediment day−1 which was similar to degradation rate in sediments with no oil. In presence of both inorganic N & P, the degradation rate increased to 47.22 ± 1.32 μg CO2-C g−1 sediment day−1. The half-saturation constant (Ks) and maximum degradation rate (Vmax) for P. aeruginosa AKS1 under increasing N and saturating P concentration were 13.57 ± 0.53 μg N g−1 sediment and 39.36 ± 1.42 μg CO2-C g−1 sediment day−1 respectively. The corresponding values at increasing P and a constant N concentration were 1.60 ± 0.13 μg P g−1 sediment and 43.90 ± 1.03 μg CO2-C g−1 sediment day−1 respectively. Similarly the degradation rate of Bacillus sp. AKS2 in sediments amended with both inorganic nutrients N & P was seven fold higher than the rates in oil only or nutrient only treated sediments. The Ks and Vmax estimates of Bacillus sp. AKS2 under increasing N and saturating P concentration were 9.96 ± 1.25 μg N g−1 sediment and 59.96 ± 7.56 μg CO2-C g−1 sediment day−1 respectively. The corresponding values for P at saturating N concentration were 0.46 ± 0.24 μg P g−1 sediment and 63.63 ± 3.54 μg CO2-C g−1 sediment day−1 respectively. The rates of CO2 production by both isolates were further stimulated when oil concentration was increased above 12.5 mg g−1 sediment. However, oil degradation activity declined at oil concentration above 40 mg g−1 sediment when treated with constant nutrient: oil ratio. Both isolates exhibited alkane hydroxylase activity but aromatic degrading catechol 1, 2-dioxygenase and catechol 2, 3-dioxygenase activities were shown by P. aeruginosa AKS1 only.

River Brahmaputra (RB) from the outer Himalayan Range and River Hooghly (RH), a distributary of River Ganga, are the two largest transboundary perennial rivers supplying freshwater to the northeastern and eastern states of India. Given the history of extensive usage of organochlorine pesticides and increasing industrialization along the banks of these rivers we investigated selected organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in the surface water of River Brahmaputra and River Hooghly. Geomean of ΣOCPs (53 ng L−1) and Σ19PCBs (108 ng L−1) was higher in RH compared with geomean of ΣOCPs (24 ng L−1) and Σ19PCBs (77 ng L−1) in RB. Among OCPs, γ-HCH showed maximum detection frequency in both the rivers reflecting ongoing lindane usage. DDT and endosulfan residues were observed at specific locations where past or ongoing sources exist. Elevated concentrations of heavier congeners (penta-hepta) were observed in those sites along RH where port and industrial activities were prevalent including informal electronic waste scrap processing units. Furthermore along River Hooghly PCB-126 was high in the suburban industrial belt of Howrah district. PCBs were found to be ubiquitously distributed in RB. Atmospheric transport of tri- and tetra-PCB congeners from the primary source regions might be a major contributor for PCBs in RB. Heavier congeners (penta-nona) in the urban centers of RB were likely due to industrial wastewater runoff from the oil refineries in the Brahmaputra valley. Σ19PCBs concentrations in this study exceeded the USEPA recommended limit for freshwater. Ecotoxicological risk assessment showed the possibility of adverse impact on the organisms in the lower trophic level due to DDT and lindane contamination. Impact of endosulfan on fishes might be of considerable concern for aquatic environment.