The present study has been undertaken in a laboratory scale to characterize and investigate pollution potential of textile effluents from DEPZ area in Dhaka, Bangladesh. Collected effluent samples from five different industries were analyzed for physico-chemical parameters using field kits and Standard Methods, and for metals using Flame Atomic Absorption Spectrophotometer (FAAS). The average physico-chemical parameters such as temperature, color, pH, DO, EC, BOD, COD, TS, total alkalinity and total hardness were found 52.4 ºC, 2646 PCU, 9.788, 1.492 mg/L, 7473.2 μS/cm, 157 mg/L, 508.8 mg/L, 9140.8 mg/L, 761.2 mg/L and 189.6 mg/L, respectively. The average concentrations of metal found in the textile effluents were in the order of Na (4611.762 mg/L) > Ca (9.166 mg/L) > Mg (3.578 mg/L) > Zn (0.113 mg/L) > Ni (0.0074 mg/L) > Cu (0.0032 mg/L). All the measured physico-chemical parameter values are negatively deviated but metal concentrations (except Na) are positively deviated from standard limits of wastewater discharge set by Department of Environment and US Environmental Protection Agency. In view of those characteristics, the textile industry effluents should be considered to be treated by setting eco-friendly effluent treatment plant (ETP) before directly discharging into the water bodies.

The aim of this study was to identify primary flow paths involved in the chlordecone (CLD) river contamination and quantify the CLD fluxes to assess CLD pollution levels and duration according to a typical catchment of the banana cropping area in the French Indies (Guadeloupe): the Perou Catchment (12 km(2)) characterized by heavy rainfall (5686 mm year(-1)). Three sub-catchments (SC1, SC2 and SC3) were studied during the hydrological year 2009-2010: a pedological survey combined with a spatialized hydrochemical approach was conducted. The average soil concentration is higher in the Perou Catchment (3400 mu g kg(-1)) than in the entire banana cropping area in Guadeloupe (2100 mu g kg(-1)). The results showed that CLD stocks in soils vary largely among soil types and farming systems: the weakest stocks are located upstream in SC1 (5 kg ha(-1)), where a majority of the area is non-cultivated; medium stocks are located in Nitisols downstream in SC3 (9 kg ha(-1)); and the greatest stocks are observed in SC2 on Andosols (12 kg ha(-1)) characterized by large farms. The annual water balance and the hydro-chemical analysis revealed that the three sub-catchments exhibited different behaviors. Perou River contamination was high during low flows, which highlighted that contamination primarily originated from groundwater contributions. The results showed that only a small part of the catchment (SC2), contributing little to the water flow, comprises a major CLD contribution, which is in agreement with the highly contaminated andosol soils observed there. Another significant result considers that at least 50 years would be required to export the totality of the actual CLD soil stocks retained in the topsoil layer. The actual time for soil remediation will however be much longer considering (i) the necessary time for the chlordecone to percolate and be stored in the shallow aquifers and (ii) its travel time to reach the river.rights reserved.

peer reviewed | The northern fulmar Fulmarus glacialis ingests a larger number of (micro)plastics than many other seabirds due to its feeding habits and gut morphology. Since 2002, they are bioindicators of marine plastics in the North Sea region, and data are needed to extend the programme to other parts of their distribution areas, such as the Arctic. In this study, we provide data on ingested plastics by fulmars collected in 1997 in Kongsfjorden, Svalbard. An extraction protocol with KOH was used and for half of the birds, the gizzard and the proventricular contents were analysed separately. Ninety-one percent of the birds had ingested at least one piece of plastic with an average of 10.3 (±11.9 SD) pieces. The gizzards contained significantly more plastics than the proventriculus. Hard fragments and polyethylene were the most common characteristics. Twelve percent of the birds exceeded the EcoQO value of 0.1 g.

In the global COVID-19 epidemic, humans are faced with a new challenge. The concept of quarantine as a preventive measure has changed human activities in all aspects of life. This challenge has led to changes in the environment as well. The air quality index is one of the immediate concrete parameters. In this study, the actual potential of quarantine effects on the air quality index and related variables in Tehran, the capital of Iran, is assessed, where, first, the data on the pollutant reference concentration for all measuring stations in Tehran, from February 19 to April 19, from 2017 to 2020, are monitored and evaluated. This study investigated the hourly concentrations of six particulate matters (PM), including PM2.5, PM10, and air contaminants such as nitrogen dioxide (NO2), sulfur dioxide (SO2), ozone (O3), and carbon monoxide (CO). Changes in pollution rate during the study period can be due to reduced urban traffic, small industrial activities, and dust mites of urban and industrial origins. Although pollution has declined in most regions during the COVID-19 quarantine period, the PM2.5 rate has not decreased significantly, which might be of natural origins such as dust. Next, the air quality index for the stations is calculated, and then, the interpolation is made by evaluating the root mean square (RMS) of different models. The local and global Moran index indicates that the changes and the air quality index in the study area are clustered and have a high spatial autocorrelation. The results indicate that although the bad air quality is reduced due to quarantine, major changes are needed in urban management to provide favorable conditions. Contaminants can play a role in transmitting COVID-19 as a carrier of the virus. It is suggested that due to the rise in COVID-19 and temperature in Iran, in future studies, the effect of increased temperature on COVID-19 can be assessed. | peer reviewed

peer reviewed | Microplastic contamination is an emerging issue in the marine environment including the Arctic. However, the occurrence of microplastics in the Arctic fjords remains less understood. Sample collections were conducted by trawling horizontally in surface water (0-0.4-m depth) and trawling vertically in the water column (0-200-m depth) to investigate the abundance, composition, and distribution of microplastics in the Rijpfjorden, Northern Svalbard, in the summer of 2017. Laser Direct Infrared chemical imaging technique was applied for the counting and identification of microplastic particles. A total of 1010 microplastic particles and 14 mesoplastics were identified from 41,038 particles in eight samples from the Rijpfjorden. The abundance of microplastics larger than 300 µm was 0.15 ± 0.19 n/m3 in surface water, and 0.15 ± 0.03 n/m3 in the water column of the Rijpfjorden. The microplastic particles identified in Rijpfjorden water consisted of 10 types of polymers. The dominant microplastics are polyurethane, polyethylene, polyvinyl acetate, polystyrene, polypropylene, and alkyd varnish. Historical ship activities and newly melted sea ice might be major sources of microplastics in the seawater of Rijpfjorden. In general, contamination of microplastics larger than 300 µm in Rijpfjorden water is at a low level in comparison to other polar waters. Further research is needed to confirm the origin and fate of microplastics below 300 µm in Arctic fjords.

An As-contaminated perched aquifer under an urban area affected by mining was studied over a year to determine the contamination source species and the mechanism of As mobilization. Results show that the dissolution of calcium arsenates in residues disposed on an inactive smelter has caused high levels of As pollution in the adjoining downgradient 6-km perched aquifer, reaching up to 158 mg/L of dissolved As, and releasing a total of ca. 7.5 tons of As in a year. Furthermore, free calcium ion availability was found to control As mobility in the aquifer through the diagenetic precipitation of calcium arsenates (Ca5H2(AsO4)4·cH2O) preventing further mobilization of As. Results shown here represent a model for understanding a highly underreported mechanism of retention of arsenate species likely to dominate in calcium-rich environments, such as those in calcareous sediments and soils, where the commonly reported mechanism of adsorption to iron(III) oxyhydroxides is not the dominant process.

Arsenic contamination of floodplain soils is extensive and additional fresh arsenic inputs to the pedosphere from human activities are ongoing.We investigate the cumulative effects of repetitive soil redox cycles, which occur naturally during flooding and draining, on a calcareous fluvisol, the native microbial community and arsenic mobility following a simulated contamination event.We show through bioreactor experiments, spectroscopic techniques and modelling that repetitive redox cycling can decrease arsenic mobility during reducing conditions by up to 45%. Phylogenetic and functional analyses of the microbial community indicate that iron cycling is a key driver of observed changes to solution chemistry. We discuss probable mechanisms responsible for the arsenic immobilisation observed in-situ. The proposed mechanisms include, decreased heterotrophic iron reduction due to the depletion of labile particulate organic matter (POM), increases to the proportion of co-precipitated vs. aqueous or sorbed arsenic with α-FeOOH/Fe(OH)3 and potential precipitation of amorphous ferric arsenate.

The performance of Cytisus striatus in association with different microbial inoculant treatments on the dissipation of the insecticide hexachlorocyclohexane (HCH) was studied. Two soils with different organic matter (A and B soil) content were spiked with 0 or 65 mg HCH kg−1. Plants were either not inoculated (NI), or inoculated with the endophyte Rhodococcus erythropolis ET54b and the HCH-degrader Sphingomonas sp. D4 separately or in combination (ET, D4 and ETD4). Unplanted pots were also established. HCH phytotoxicity was more pronounced in the B soil. Soil HCH concentrations in unplanted pots were similar to initial concentrations, whereas concentrations were reduced after plant growth: by 20% and 8% in A and B soil, respectively. Microbial inoculants also modified HCH dissipation, although effects were soil-dependent. Inoculation with the combination of strains (ETD4) led to a significant enhancement in HCH dissipation: up to 53% in the A soil and 43% in the B soil.

In this study, tropical cyclones over the East and South China Seas were found to be the most predominant weather conditions associated with the occurrence of high ozone (O3) episodes in Hong Kong in 2005–2009. A photochemical trajectory model coupled with Master Chemical Mechanism (MCM) was adapted to simulate the O3 concentrations during two O3 pollution episodes. The results agreed well with the observed data. A representative backward air mass trajectory was used to determine the contribution of each volatile organic compound (VOC) to the O3 levels. After taking into account both reactivity and mass emission of each VOC, 10 species were found to be the key O3 precursors in Hong Kong. Further analysis identified solvent related products accounting for 70% of the modeled O3 concentration in Hong Kong. The results highlight the importance of considering together reactivity and source sector emissions in developing targeted VOC reduction for O3 abatement strategies.

Here, we report on a two-years field experiment aimed at the quantification of the emissions of nitrous oxide (N2O) and methane (CH4) from the dominant wheat–maize double cropping system in North China Plain. The experiment had 6 different fertilization strategies, including a control treatment, recommended fertilization, with and without straw and manure applications, and nitrification inhibitor and slow release urea. Application of N fertilizer slightly decreased CH4 uptake by soil. Direct N2O emissions derived from recommended urea application was 0.39% of the annual urea-N input. Both straw and manure had relatively low N2O emissions factors. Slow release urea had a relatively high emission factor. Addition of nitrification inhibitor reduced N2O emission by 55%. We conclude that use of nitrification inhibitors is a promising strategy for N2O mitigation for the intensive wheat–maize double cropping systems.