The establishment of an efficient surface water quality monitoring (WQM) network is a critical component in the assessment, restoration and protection of river water quality. A periodic evaluation of monitoring network is mandatory to ensure effective data collection and possible redesigning of existing network in a river catchment. In this study, the efficacy and appropriateness of existing water quality monitoring network in the Kabbini River basin of Kerala, India is presented. Significant multivariate statistical techniques like principal component analysis (PCA) and principal factor analysis (PFA) have been employed to evaluate the efficiency of the surface water quality monitoring network with monitoring stations as the evaluated variables for the interpretation of complex data matrix of the river basin. The main objective is to identify significant monitoring stations that must essentially be included in assessing annual and seasonal variations of river water quality. Moreover, the significance of seasonal redesign of the monitoring network was also investigated to capture valuable information on water quality from the network. Results identified few monitoring stations as insignificant in explaining the annual variance of the dataset. Moreover, the seasonal redesign of the monitoring network through a multivariate statistical framework was found to capture valuable information from the system, thus making the network more efficient. Cluster analysis (CA) classified the sampling sites into different groups based on similarity in water quality characteristics. The PCA/PFA identified significant latent factors standing for different pollution sources such as organic pollution, industrial pollution, diffuse pollution and faecal contamination. Thus, the present study illustrates that various multivariate statistical techniques can be effectively employed in sustainable management of water resources. Highlights • The effectiveness of existing river water quality monitoring network is assessed• Significance of seasonal redesign of the monitoring network is demonstrated• Rationalization of water quality parameters is performed in a statistical framework.

In this work, principal component analysis/multiple linear regression (PCA/MLR), positive matrix factorization (PMF), and UNMIX model were employed to apportion potential sources of polycyclic aromatic hydrocarbons (PAHs) in surface sediments from middle and lower reaches of the Yellow River, based on the measured PAHs concentrations in sediments collected from 22 sites in November 2005. The results suggested that pyrogenic sources were major sources of PAHs. Further analysis indicated that source contributions of PAHs compared well among PCA/MLR, PMF, and UNMIX. Vehicles contributed 25.1–36.7 %, coal 34.0–41.6 %, and biomass burning and coke oven 29.2–33.2 % of the total PAHs, respectively. Coal combustion and traffic-related pollution contributed approximately 70 % of anthropogenic PAHs to sediments, which demonstrated that energy consumption was a predominant factor of PAH pollution in middle and lower reaches of the Yellow River. In addition, the distributions of contribution for each identified source category were studied, which showed similar distributed patterns for each source category among the sampling sites.

The spatial and temporal variations in copepod communities were investigated during four oceanographic cruises conducted between July 2005 and March 2007 aboard the R/V Hannibal. A close relationship was observed between the temperature, salinity, hydrographic properties and water masses characterising the Gulf of Gabes. Indeed, water thermal stratification began in May–June, and a thermocline was established at a 20-m depth, but ranged from 25 m in July to more than 30 m in September. The zooplankton community is dominated by copepods representing 69 % to 83 % of total zooplankton. Spatial and temporal variation of copepods in relation to environmental factors shows their close relationship with the hydrodynamic features of the water column. Thermal stratification in the column, established in summer, supports copepod development. In fact, copepod abundance increases gradually with rising water temperature and salinity, starting from the beginning of thermal stratification (May–June 2006) and lasting until its completion (July 2005 and September 2006). When the water column is well mixed (March 2007), copepod abundance decreased. Our finding shows that temperature and salinity seem to be the most important physical factors and thus strongly influence the taxonomic diversity and distribution of the copepod population. They are characterised by the dominance of Oithona nana, representing 75–86 % of total cyclopoid abundance. The most abundant species during the stratification period were O. nana, Acartia clausi and Stephos marsalensis in July 2005 and September 2006. However, during the mixing period, Euterpina acutifrons was more abundant, representing 21 % of the total. Unlike the copepod community, which is more abundant during the period of high stratification, phytoplankton proliferates during semi-mixed conditions.

Hexabromocyclododecane (HBCD) is a globally produced brominated flame retardant used primarily as an additive flame retardant in polystyrene and textile products. Photodegradation of HBCD in the presence of Fe(III)-carboxylate complexes/H₂O₂ was investigated under simulated sunlight. The degradation of HBCD decreased with increasing pH in the Fe(III)-oxalate solutions. In contrast, the optimum pH was 5.0 for the Fe(III)-citrate-catalyzed photodegradation within the range of 3.0 to 7.0. For both Fe(III)-oxalate and Fe(III)-citrate complexes, the increase of carboxylate concentrations facilitated the photodegradation. The photochemical removal of HBCD was related to the photoreactivity and speciation distribution of Fe(III) complexes. The addition of H₂O₂ markedly accelerated the degradation of HBCD in the presence of Fe(III)-citrate complexes. The quenching experiments showed that ·OH was responsible for the photodegradation of HBCD in the Fe(III)-carboxylate complexes/H₂O₂ solutions. The results suggest that Fe(III) complexes/H₂O₂ catalysis is a potential method for the removal of HBCD in the aqueous solutions.

This research investigated the 1,4-dioxane (1,4-D) degradation efficiency and rate during persulfate oxidation at different temperatures, with and without Fe²⁺addition, also considering the effect of pH and persulfate concentration on the oxidation of 1,4-D. Degradation pathways for 1,4-D have also been proposed based on the decomposition intermediates and by-products. The results indicate that 1,4-D was completely degraded with heat-activated persulfate oxidation within 3–80 h. The kinetics of the 1,4-D degradation process fitted well to a pseudo-first-order reaction model. Temperature was identified as the most important factor influencing the 1,4-D degradation rate during the oxidation process. As the temperature increased from 40 to 60 °C, the degradation rate improved significantly. At 40 °C, the addition of Fe²⁺also increased the 1,4-D degradation rate. Interestingly, at 50 and 60 °C, the 1,4-D degradation rate decreased slightly with the addition of Fe²⁺. This reduced degradation rate may be attributed to the rapid conversion of Fe²⁺to Fe³⁺and the production of an Fe(OH)₃precipitate which limited the ultimate oxidizing capability of persulfate with Fe²⁺under higher temperatures. Higher persulfate concentrations led to higher 1,4-D degradation rates, but pH adjustment had no significant effect on the 1,4-D degradation rate. The identification of intermediates and by-products in the aqueous and gas phases showed that acetaldehyde, acetic acid, glycolaldehyde, glycolic acid, carbon dioxide, and hydrogen ion were generated during the persulfate oxidation process. A carbon balance analysis showed that 96 and 93 % of the carbon from the 1,4-D degradation were recovered as by-products with and without Fe²⁺addition, respectively. Overall, persulfate oxidation of 1,4-D is promising as an economical and highly efficient technology for treatment of 1,4-D-contaminated water.

Thermal desorption is widely used for remediation of soil contaminated with volatiles, such as solvents and distillates. In this study, a soil contaminated with semivolatile polychlorinated biphenyls (PCBs) was sampled at an interim storage point for waste PCB transformers and heated to temperatures from 300 to 600 °C in a flow of nitrogen to investigate the effect of temperature and particle size on thermal desorption. Two size fractions were tested: coarse soil of 420–841 μm and fine soil with particles <250 μm. A PCB removal efficiency of 98.0 % was attained after 1 h of thermal treatment at 600 °C. The residual amount of PCBs in this soil decreased with rising thermal treatment temperature while the amount transferred to the gas phase increased up to 550 °C; at 600 °C, destruction of PCBs became more obvious. At low temperature, the thermally treated soil still had a similar PCB homologue distribution as raw soil, indicating thermal desorption as a main mechanism in removal. Dechlorination and decomposition increasingly occurred at high temperature, since shifts in average chlorination level were observed, from 3.34 in the raw soil to 2.75 in soil treated at 600 °C. Fine soil particles showed higher removal efficiency and destruction efficiency than coarse particles, suggesting that desorption from coarse particles is influenced by mass transfer.

Hospitals are considered as a special and important type of indoor public place where air quality has significant impacts on potential health outcomes. Information on indoor air quality of these environments, concerning exposures to particulate matter (PM) and related toxicity, is limited though. This work aims to evaluate risks associated with inhalation exposure to ten toxic metals and chlorine (As, Ni, Cr, Cd, Pb, Mn, Se, Ba, Al, Si, and Cl) in coarse (PM₂.₅–₁₀) and fine (PM₂.₅) particles in a Portuguese hospital in comparison with studies representative of other countries. Samples were collected during 1 month in one urban hospital; elemental PM characterization was determined by proton-induced X-ray emission. Noncarcinogenic and carcinogenic risks were assessed according to the methodology provided by the United States Environmental Protection Agency (USEPA; Region III Risk-Based Concentration Table) for three different age categories of hospital personnel (adults, >20, and <65 years) and patients (considering nine different age groups, i.e., children of 1–3 years to seniors of >65 years). The estimated noncarcinogenic risks due to occupational inhalation exposure to PM₂.₅-bound metals ranged from 5.88 × 10⁻⁶for Se (adults, 55–64 years) to 9.35 × 10⁻¹for As (adults, 20–24 years) with total noncarcinogenic risks (sum of all metals) above the safe level for all three age categories. As and Cl (the latter due to its high abundances) were the most important contributors (approximately 90 %) to noncarcinogenic risks. For PM₂.₅–₁₀, noncarcinogenic risks of all metals were acceptable to all age groups. Concerning carcinogenic risks, for Ni and Pb, they were negligible (<1 × 10⁻⁶) in both PM fractions for all age groups of hospital personnel; potential risks were observed for As and Cr with values in PM₂.₅exceeding (up to 62 and 5 times, respectively) USEPA guideline across all age groups; for PM₂.₅–₁₀, increased excess risks of As and Cr were observed particularly for long-term exposures (adults, 55–64 years). Total carcinogenic risks highly (up to 67 times) exceeded the recommended level for all age groups, thus clearly showing that occupational exposure to metals in fine particles pose significant risks. If the extensive working hours of hospital medical staff were considered, the respective noncarcinogenic and carcinogenic risks were increased, the latter for PM₂.₅exceeding the USEPA cumulative guideline of 10⁻⁴. For adult patients, the estimated noncarcinogenic and carcinogenic risks were approximately three times higher than for personnel, with particular concerns observed for children and adolescents.

Quality improvement of acidic soil (with an initial pH of approximately 4.5) with respect to soil pH, exchangeable cations, organic matter content, and maize growth was attempted using natural (NSF) and calcined starfish (CSF). Acidic soil was amended with NSF and CSF in the range of 1 to 10 wt.% to improve soil pH, organic matter content, and exchangeable cations. Following the treatment, the soil pH was monitored for periods up to 3 months. The exchangeable cations were measured after 1 month of curing. After a curing period of 1 month, the maize growth experiment was performed with selected treated samples to evaluate the effectiveness of the treatment. The results show that 1 wt.% of NSF and CSF (700 and 900 °C) were required to increase the soil pH to a value higher than 7. In the case of CSF (900 °C), 1 wt.% was sufficient to increase the soil pH value to 9 due to the strong alkalinity in the treatment. No significant changes in soil pHs were observed after 7 days of curing and up to 3 months of curing. Upon treatment, the cation exchange capacity values significantly increased as compared to the untreated samples. The organic content of the samples increased upon NSF treatment, but it remains virtually unchanged upon CSF treatment. Maize growth was greater in the treated samples rather than the untreated samples, except for the samples treated with 1 and 3 wt.% CSF (900 °C), where maize growth was limited due to strong alkalinity. This indicates that the amelioration of acidic soil using natural and calcined starfish is beneficial for plant growth as long as the application rate does not produce alkaline conditions outside the optimal pH range for maize growth.

The discharge of untreated or inadequately treated effluents has been identified among the activities responsible for the spread of a wide range of potentially infectious agents. The aim of this study was to determine whether inadequate treatment of wastewater and the faecal pollution load of effluents and receiving water bodies in Sedibeng District and Soshanguve peri-urban area of the Tshwane Metropolitan Municipality could be a potential threat to the health of the surrounding communities. Variations in the counts of faecal indicator bacteria and pathogenic microorganisms and compliance of the effluents and receiving water bodies with South African and World Health Organization standards were assessed between August 2011 and May 2012 using culture-based methods and molecular techniques. The overall quality of effluents did not comply with the South African special standard of no risk for unrestricted irrigation (zero Escherichia coli/100 ml). The quality of the receiving water bodies did not comply with South African regulatory limits set for domestic purposes (zero E. coli/100 ml, <30 faecal enterococci/100 ml and <1 somatic coliphages/100 ml), for full contact recreation (<20 somatic coliphages/100 ml) and aquaculture (<10 E. coli/100 ml) and WHO standards for full and intermediate contact recreational use (<1 E. coli/100 ml and <40 faecal enterococci/100 ml, respectively). The PCR results revealed the prevalence of pathogenic microorganisms; between 0 and 60 % of samples tested positive for Salmonella Typhimurium and Shigella dysenteriae, and between 20 and 60 % of samples tested positive for Vibrio cholerae. These findings demonstrated that potential health risks might be associated with the use of the target river waters for domestic, recreational and irrigation purposes. This study calls for a prompt intervention to improve wastewater management.

Marine macroalgae have evolved a different mechanism to maintain physiological concentrations of essential metal ions and non-essential metals. The objective of the present work was to evaluate the antioxidant response and DNA damage of copper and cadmium ions in three halophytes, namely, Acanthophora spicifera, Chaetomorpha antennina, and Ulva reticulata. Accumulation of copper was significantly higher (P < 0.05) than that of cadmium. Biochemical responses showed that copper was considerably more toxic than cadmium (P < 0.05). Decreases in glutathione content and fluctuations of super oxide dismutase, catalase, and glutathione peroxidase activities were observed corresponding to time and concentration of exposure. Interestingly, it was also observed that antioxidant levels decreased as a result of metal accumulation, which may be due to free radicals generated by copper and cadmium in seaweeds. The present study also showed that copper and cadmium increased oxidative stress and induced antioxidant defense systems against reactive oxygen species. The order of toxicity for metals in the studied seaweeds was U. reticulata > A. spicifera > C. antennina. DNA damage index analysis supported that copper was significantly (P < 0.05) more toxic than cadmium. Bioaccumulation, biochemical responses, and DNA damage observed in the here analyzed marine macroalgae after exposure to selected metals indicate that these marine organisms represent useful bioindicators of marine pollution.