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The increased load of plastic in waste streams after the COVID-19 pandemic outbreak has increased the possibility of microplastics (MPs) contamination channelling through the rivers and infiltrating the aquatic ecosystems. MPs in packaged water, community-stored water, groundwater, and surface water of Kaveri River (KR), Thamirabarani River (TR), Adyar River (AR), and Cooum River (CR) in Tamil Nadu were therefore investigated about 2 years after the COVID-19 pandemic outbreak. Using μFTIR and μRaman spectroscopy, polyamide, polypropylene, polyethylene, ethylene vinyl alcohol copolymer resin, and polyvinyl chloride were identified as the primary polymer types. The average number of MPs was 2.15 ± 1.9 MP/L, 1.1 ± 0.99 MP/L, 5.25 ± 1.15 MP/L, and 4 ± 2.65 MP/L in KR, TR, AR, and CR, respectively, and 1.75 ± 1.26 MP/L in groundwater, and 2.33 ± 1.52 MP/L in community stored water. Only LDPE was detected in recycled plastic-made drinking water bottles. More than 50% of MPs were found to be of size less than 1 mm, with fibrous MPs being the prevalent type, and a notable prevalence of blue-coloured microplastics in all the sample types. The Pollution Load Index (PLI) was >1 in all the rivers. Toxicity rating based on the polymer risk index (PORI) categorized AR and TR at medium risk (category II), compared to KR and CR at considerable risk (category III). Overall pollution risk index (PRI) followed a decreasing trend with CR > AR > KR > TR of considerable to low-risk category. Ecological risk assessment indicates a negligible risk to freshwater biota, except for four sites in the middle and lower stretches of Adyar River (AR - 2, AR - 4) and upper and lower stretches of Cooum River (CR - 1, CR - 3), located adjacent to direct sewer outlets, and one location in the lower stretch of Kaveri River (KR - 9), known for fishing and tourist activities., Competing Interests: Declaration of competing interest The authors declare no financial and non-financial competing interests., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Hooghly River (HR), the other name used for the lower stretch of River Ganga, is a prime freshwater source in the eastern part of India. However HR has been evidenced with a variety of emerging organic pollutants (EOPs) in the recent past. Given the extensive use of plasticizers and additive in plastic products, we have investigated seven plasticizers and bisphenol A (BPA) in the surface and storm-water of HR up to the tip of the Bay of Bengal. Further using a previously published sediment data we have estimated the fluxes for the aforementioned EOPs. Surface water and storm-water concentrations of seven plasticizers varied between 92.62 and 770 ng/L (176.1 ± 104.8; Avg ± SD) and 120.9-781.5 ng/L (355.2 ± 232.5), respectively. BPA varied between 43 and 8800 ng/L (658.3 ng/L ± 1760) and 117.9-2147 ng/L (459.3 ± 620.2) in surface and storm-water, respectively. With the increase in salinity, a decreasing trend for bis-(2-ethylhexyl) phthalate (DEHP) was evidenced. However, concentration of BPA increased with the increase in salinity. Significant and strong correlation between DEHP and BPA (R 2  = 0.6; p < 0.01) in the suburban corridor might have resulted from sludge disposal of the scrap recycling activities. Using site-specific principal component analysis, unregulated disposal of plastic waste, particularly from such industrial belts and tourist spots were identified as the possible point sources for plasticizers and BPA in this region. Net diffusive flux based on fugacity fraction showed a trend depending on the pollutant's aqueous solubility and partition coefficient. However, transfer tendency from water to sediment was noticed in the sites having point source. Estimated ecotoxicological risk posed by BPA was higher for edible fishes and for lower order organisms, PAEs was the major contributor., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

The transboundary River Ganga serves as a conduit for meltwater from the Himalayas and is a major freshwater source for two thirds of Indian population before emptying into the Sundarban Delta, the largest estuary in the Bay of Bengal. Endocrine disrupting compounds (EDCs) such as phthalic acid esters (PAEs) and bisphenol A (BPA) used as organic plastic additives can pollute the aquatic environment receiving plastic litter. Hence, we have investigated these EDCs in water samples from Ganga and Sundarban wetland of India. Since these compounds exhibit estrogenic potential, we have further measured steroids and evaluated the estrogenic activity (estradiol equivalents, BioE2Eqs) using an in-vitro bioassay (E-Screen). Further BioE2Eqs were compared with the sum of predicted estradiol equivalents based on the chemical concentrations of PAEs and BPA by E-Screen (ChemE2Eq) and YES factors (ChemYES). Caffeine was measured as a marker for anthropogenic wastewater discharge. Results showed that the highest BioE2Eq (below the lowest observable effect of E2 on fish) was associated with sites having sewer outfalls in the middle stretch of the river, and concomitantly coinciding with the elevated concentrations of caffeine. Neither ChemE2Eq nor ChemYES correlated with measured BioE2Eqs. River concentrations of BPA (0.04-4.46 µg/L) and ∑ 7 plasticizers (0.43-7.63 µg/L) were higher than BPA (0.21-2.82 µg/L) and ∑ 7 plasticizers (0.85-2 µg/L) in the Sundarban wetland. The only steroids detected were androgens, found at four sites in Ganga (0.007 µg/L± 0.003, mean ± S.D.). The highest estimated ecotoxicological risk to aquatic insect and fish stemmed from BPA. A secondary effect, and a potential impact on human health could be reflected via fish consumption from the productive fisheries region along the lower stretch of River Ganga. Identification of areas of elevated estrogenicity, plasticizer and steroid concentrations in River Ganga can be used to design and implement interventions for the remediation of such emerging contaminants., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Soil and sludge are major reservoirs of organic compounds such as fluoroquinolones (FQs) which are broad-spectrum antibacterial agents. Hence, we monitored three major FQs, namely, ciprofloxacin (CIP), norfloxacin (NOR), and ofloxacin (OFL), in surface soil from two major dumpsites and dry and wet sludge from sewage treatment plants in Chennai city. The mean concentration of FQs in soil and sludge samples were 20 μg/g and 26 μg/g, respectively. Nearly 50% of the total FQs in dumpsite soil was contributed by CIP followed by NOR (32%) and OFL (13%). Similarly, CIP was the major contributor in sludge samples followed by NOR and OFL. The concentration of FQs was two folds higher in wet sludge than dry sludge most likely indicating that water solubility of these compounds might play an important role for elevated level of FQs in wet sludge. Solid waste from pharmaceutical industries, households, and sludge from wastewater treatment plants were expected to be the major source of FQs in dumpsite soil. Predicted risk assessment using soil to water migration concentrations via surface run off indicated high risk to aquatic organisms. However, risk quotient (RQ) was found less to earthworm in most of the soil samples. The findings from this study might help in future policies on disposal of household antibiotics in the solid waste stream., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Adyar and Cooum, the two rivers intersecting Chennai city, are exposed to serious pollution due to the release of large quantities of dumped waste, untreated wastewater and sewage. Sediments can act as repository for emerging organic contaminants. Hence, we have monitored the occurrence and risk associated with plasticizers [six phthalic acid esters (PAEs), bis(2-ethyl hexyl adipate) (DEHA)] and bisphenol A (BPA) in surface riverine sediments of Adyar and Cooum rivers from residential/commercial, industrial and electronic waste recycling sites. Σ 7 plasticizers (PAEs + DEHA) in the Adyar riverine sediment (ARS) and Cooum riverine sediment (CRS) varied between 51.82-1796 and 28.13-856 ng/g, respectively. More than three-fourth of Σ 7 plasticizers came from bis(2-ethylhexyl) phthalate (DEHP), in accordance with the high production and usage of this compound. BPA varied between 10.70-2026 and 7.58-1398 ng/g in ARS and CRS, respectively. Average concentrations of plasticizers and BPA were four times higher in electronic waste (e-waste) recycling sites when compared with industrial and residential/commercial sites. BPA and DEHP showed a strong and significant correlation (R 2  = 0.7; p < 0.01) in the e-waste sites thereby indicating common source types. Sites present at close proximity to raw sewage pumping stations contributed to 70% of the total BPA observed in this study. For the derived pore water concentration of plasticizers and BPA, the ecotoxicological risk has been found to be higher in ARS over CRS. However, sediment concentrations in all the sites of ARS and CRS were much below the recommended serious risk concentration for human (SRC human ) and serious risk concentration for ecotoxicological (SRC eco ).

The Hooghly River (HR) estuary is the first deltaic off-shoot of the perennial and transboundary river, Ganga, India. HR receives industrial and domestic waste along with storm-water run-off from Kolkata city and the adjoining districts. Organic micropollutants (OMPs) have been collectively termed for plasticizers, pharmaceuticals and personal care products, which are extensively consumed and disposed in the waste streams. Hence emerging OMPs were investigated to obtain the first baseline data from the Hooghly riverine sediment (HRS) along urban and suburban transects using gas chromatography mass spectrometry (GC-MS). The concentration range of OMPs in the HRS varied between 3 and 519 ng/g for carbamazepine, 5-407 ng/g for non-steroidal anti-inflammatory drugs (NSAIDs), 2-26 ng/g for musk ketone, 2-84 ng/g for triclosan, 2-199 ng/g for bisphenol A (BPA), 2-422 ng/g for plasticizers (phthalic acid esters (PAEs) and bis (2-ethylhexyl) adipate (DEHA)) and 87-593 ng/g for parabens. Carbamazepine concentration in sediment was an useful marker for untreated wastewater in urban waterways. High concentrations of BPA and PAEs in the suburban industrial corridor together with significant correlation between these two type of OMPs (r 2  = 0.5; p < 0.01) likely reflect a common source, possibly associated with the plastic and electronic scrap recycling industries. Among all the categories of OMPs, plasticizers seems to exhibit maximum screening level ecological risk through out the study area., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

This work focused on photo-assisted crude peroxidase mediated transformations of chlorinated phenols (CPs) from spiked and industrial wastewaters and the identification of reaction products formed. Garden radish Raphanus sativus was the source of crude peroxidase. No chlorine bearing compounds were detected by gas chromatography-high resolution mass spectrometry analysis. Under identical test conditions, the concentrations of 4-chlorophenol and 2,4-dichlorophenol were demoted to zero from 514 mg/L, 652 mg/L and that of 2,4,6-trichlorophenol and pentachlorophenol were reduced to 18 mg/L and 37 mg/L from 790 mg/L and 1066 mg/L, respectively (high-pressure liquid chromatography analysis). Chloride ion release profiles also showed a progressively increasing trend. A neat chemical oxygen demand removal to the extent of 63-79% was achieved in the case of spiked wastewater sample and to the extent of 77% for industrial wastewaters. A hypothesis reaction scheme was also suggested to comprehend the mechanism of degradation reactions.

This study investigated the presence of total mercury (Hg) and organic mercury levels in the muscle of 19 common fresh water fish species captured from river Ganges, West Bengal, India. The total mercury level found in our study may not cause any toxic effect, but the methyl mercury (MeHg) level in some freshwater fish species was surprisingly very high and toxically unacceptable. The results of mercury analysis in various specimens indicated that some fish muscles tended to accumulate high levels of Hg, and approximately 50-84% of Hg was organic mercury. A strong positive correlation between mercury levels in muscle with food habit and fish length (age) was found. Wallago attu possessed the highest amount of organic mercury in their muscle tissues, and it was 0.93 ± 0.61 μg Hg/g of wet weight. Whereas in small-sized fishes Eutropiichthys murius, Puntius sarana, Cirrhinus mrigala, Mystus vittatus or Mystus gulio, and Tilapia mossambicus, it was below the detection limit. Contamination in Catla catla (0.32 ± 0.11), Anguilla bengalensis bengalensis (0.26 ± 0.07 μg Hg/g), Chitala chitala (0.25 ± 0.18), Rita rita (0.34 ± 0.14), and Ompok pabda (0.26 ± 0.04) was also above the 0.25 μg Hg/g of wet weight, the limit set by the PFA for the maximum level for consumption of fish exposed to MeHg. Though in Labeo rohita (0.12 ± 0.03), Mastacembelus armatus (0.17 ± 0.02), Pangasius pangasius (0.12 ± 0.16), Bagarius bagarius (0.12 ± 0.01), and Clupisoma garua (0.1 ± 0.01), concentration was below the recommended level, in Lates calcarifer (0.23 ± 0.0) and Mystus aor (0.23 ± 0.1), it was threatening. Interestingly, a low concentration of Hg was found in post-monsoon samples.

Static renewal bioassay tests were conducted to evaluate the acute toxicity of two neem based biopesticides, applied widely on tea plantation namely, Nimbecidine and Neem Gold either separately as well as, in combination to the fingerlings (mean body length- 4.46 +/- 0.15 cm; mean body weight- 0.49 +/- 0.15g) of a fresh water loach, Lepidocephalichthys guntea (Hamilton Buchanan) acclimatized to laboratory conditions prior to experiment. The 96 hours LC50 values for Nimbecidine and Neem Gold and the combination of the two were 0.0135 mgl(-1), 0.0525mgl(-1) and 0.0396 mgl(-1), respectively. The regular water quality analysis showed, that with increasing doses of biopesticides, dissolved oxygen level was lower and other parameters like pH, free carbon dioxide, total alkalinity total hardness, chloride ions of water increased. The fish under toxicity stress suffered several abnormalities such as erratic and rapid movement, body imbalance and surface floating responding proportionately to the increase in concentrations of the toxicant biopesticides. The 96 hours LC50 values proved Nimbecidine more toxic than Neem Gold and the combination of the two biopesticides.