The high levels of indoor particulate matter in developing countries and the apparent scale of its impact on the global burden of disease underline the importance of particulate matter as an environmental health risk and the consequent need for monitoring them particularly in indoor school microenvironments. The concentrations of PM10, PM2.5, and PM1.0, were measured along with ionic concentrations K+, Ca2+, Na+, Mg2+, SO42–, NO3–, Cl– and F– collected from settled dust in the indoor–outdoor environment of roadside and residentially located schools in Agra City, from January to May 2008–09. Along with PM concentrations at the roadside and residentially located schools meteorological parameters like temperature, humidity, and wind speed and air exchange rate was also calculated during the study period. The enrichment factor was calculated using Ca as a reference to the trace ionic species to identify the sources. Principle component analysis showed three to two factors inside and three factors outside the classrooms of the roadside and residentially located schools. These factors reflected sources like soil dust, road dust, vehicle emissions, anthropogenic sources, industrial emissions, metal processes, and incineration activities and their contributions were estimated using principal component analysis. Symptoms like asthma, dizziness, coughing, itching, eye irritation, shortness of breath, headache, cold and flu were observed. Measurements of such exposure levels would be helpful in the prevention of environmental risks to school children.

The extent of microplastic pollution (<5mm) in the southern hemisphere, particularly southern Africa, is largely unknown. This study aimed to evaluate microplastic pollution along the south-eastern coastline of South Africa, looking at whether bays are characterised by higher microplastic densities than open stretches of coastline in both beach sediment and surf-zone water. Microplastic (mean±standard error) densities in the beach sediment ranged between 688.9±348.2 and 3308±1449particles·m−2, while those in the water column varied between 257.9±53.36 and 1215±276.7particles·m−3. With few exceptions there were no significant spatial patterns in either the sediment or water column microplastic densities; with little differences in density between bays and the open coast (P>0.05). These data indicate that the presence of microplastics were not associated with proximity to land-based sources or population density, but rather is governed by water circulation.

The aims of this work are to provide an overview of the current stresses of estuaries in Argentina and to propose adaptation strategies from an ecohydrological approach. Several Argentinian estuaries are impacted by pollutants, derived mainly from sewage discharge and agricultural or industrial activities. Anthropogenic impacts are expected to rise with increasing human population. Climate-driven warmer temperature and hydrological changes will alter stratification, residence time, oxygen content, salinity, pollutant distribution, organism physiology and ecology, and nutrient dynamics. Good water quality is essential in enhancing estuarine ecological resilience to disturbances brought on by global change. The preservation, restoration, and creation of wetlands will help to protect the coast from erosion, increase sediment accretion rates, and improve water quality by removing excess nutrients and pollutants. The capacity of hydrologic basin ecosystems to absorb human and natural impacts can be improved through holistic management, which should consider social vulnerability in complex human–natural systems.

In order to evaluate the spatial distribution and potential ecological risk of Pb, Cu, Zn, Cd, and Hg, the surface sediments were collected from 18 sites in the Shuangtaizi estuary. The concentrations of Pb, Cu, Zn, Cd, and Hg were analyzed by atomic absorption spectrophotometry and atomic fluorescence spectrometry after digestion. The particle sizes of the sediments were analyzed using a laser diffraction particle size analyzer. The results show that the heavy metal contents in the sediments are observed in the following order: Zn (18.25–126.75mg/kg)>Pb (4.38–9.65mg/kg)>Cu (1.80–17.68mg/kg)>Cd (0.241–0.764mg/kg)>Hg (0.007–0.021mg/kg). In comparison with the concentrations of heavy metals in other regions, the concentrations of Pb, Cu, and Zn in the Shuangtaizi estuary are generally low, and the Cd concentrations are close to those reported in other regions. Both the potential ecological risk index and the geoaccumulation index reveal that the heavy metal pollution in Shuangtaizi estuary is mainly dominated by Cd.

An integrated approach for the assessment of coastal sediment quality was utilised in three areas of Sardinia (Western Mediterranean, Italy). Sediments were analysed for trace metals and polycyclic aromatic hydrocarbons (PAHs), while benthic foraminifera were used as bioindicators. Furthermore, the embryo-toxicity test was used to provide ecologically relevant information using rapid and cost-effective screening tools. The aim was to evaluate the usefulness of coupling different analytical tools. The results revealed the presence of polluted sediments in areas exposed to petrochemical industries, smelters or military settlements. However, while foraminifera have presented similar indications for chemical analysis of contamination levels in the different areas, the toxicity test exhibited a poor relationship with the contaminants measured individually. The results raise questions concerning the bioavailability of contaminants released by sediments in the water column. Overall, the toxicity rate was significant in many samples in comparison with other sites studied in other Mediterranean regions.

The occurrence and distribution of tributyltin (TBT) and alternative biocides were investigated in sediment from semi-enclosed bays, fishing ports, and large commercial harbors in Korea. Extremely high concentration of TBT (55,264ngSn/g) was detected near a large shipyard, even after a total ban on its use in Korea. Diuron was the biocide with the highest detection frequency and concentration levels, followed by Irgarol 1051. Sea-Nine 211 was detected at 3 of 32 stations surveyed. Dichlofluanid, zinc and copper pyrithiones levels were below the detection limits at all the stations surveyed. The relatively high levels of Diuron (9–62.3ng/g) and Irgarol 1051 (1.5–11.5ng/g) were detected in harbor and shipyard areas. Diuron and Irgarol 1051 levels including TBT in sediments from hot spots in Korea exceeded global sediment quality guidelines.

Intensive mariculture results in a rise in nutrient concentrations, then leads to serious eutrophication in coastal waters. Based on the sampling data obtained between August 2012 and July 2013, the eutrophication status in Yantian Bay was assessed, and the proportion of marine animals co-cultured with seaweeds was evaluated. The nutritional quality index (NQI) ranged from 4.37 to 13.20, indicating serious eutrophication conditions. The annual average ratio of nitrogen/phosphorus (N/P) was 25.19, indicating a nitrogen surplus in this system. DIN was selected as the best parameter to balance seaweed absorption and marine animal DIN production. Gracilaria lemaneiformis and Laminaria japonica were selected as co-cultured seaweeds. The optimal proportion of G. lemaneiformis production was assessed as 20074.14 tonnes. The optimal proportion of L. japonica production was evaluated as 15890.68 tonnes. High-temperature adapted seaweeds should be introduced for removing nutrients releasing by farmed aquatic animals in the summer in Yantian Bay.

Ten surface sediments were collected from the open Indian Ocean at depths below 4000m in 2011, for the analysis of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs). The concentrations of Σ32 PCBs, Σ7 PBDEs, and BDE-209 were 120–514, 49–152, and 7–133pg/g, respectively. These concentrations are close to the lowest values recorded in the global marine environment. The PCBs had a relatively uniform composition, and were dominated by low chlorinated congeners. The concentrations of di-, tri-, and tetra-PCBs were strongly correlated with the total organic carbon (TOC), suggesting the dissolved PCBs were derived from the atmosphere via diffusive air–water exchange, and absorbed by phytoplankton. A high proportion of BDE209 was only detected in the sediment of the low fan of the Ganga River. There were weak correlations between low brominated BDEs and TOC, implying the degradation of BDE209 is a possible source of lower-brominated BDEs in deep-sea sediments.

In order to evaluate the ability of granulated coal ash (GCA), a byproduct of coal thermal electric power stations, to remove hydrogen sulfide from organically enriched sediments, a pilot study was carried out at oyster farming sites, where sediments were enriched with oyster feces and dead oysters. Concentration of hydrogen sulfide in the interstitial water of the sediment decreased to nearly zero in both experimental sites, whereas it remained over 0.2mg/l in the control site. Concentration of acid volatile sulfide (AVS) in the sediment also decreased significantly in both experimental sites, while remained over 0.4mg/g in the control site. Increases were observed in both the number of benthic microalgae species and the individual number of benthic animals in the surface sediments. This may have been due to the decrease in hydrogen sulfide.

The oxidizing capacity of the atmosphere, defined as the global mean tropospheric abundance of the hydroxyl radical (OH·), strongly influences air pollution by controlling the lifetimes of gaseous pollutants and the production of particulate matter. Predicting future changes in OH· due to anthropogenic emissions and climate change is of interest to air quality managers, but it is difficult because of multiple competing effects. Models of atmospheric chemistry suggest that these competing effects buffer significant change in OH· in the past and in the near future. However, proxy-based observations for past changes in OH· and other oxidants over the preindustrial-industrial and glacial-interglacial time scales suggest much larger changes than models estimate. Model sensitivity studies show that variability in past and future OH· is highly sensitive to relative emissions of reactive nitrogen and carbon, water vapor, lightning, and stratospheric ozone, implying that one or more of these variables is highly sensitive to climate.