Purpose Recent evidence indicates that exposure to persistent organic pollutants (POPs) is emerging as an important risk factor for atherosclerosis-related diseases, including stroke. Hypertension (HTN) is a major risk factor for stroke, and some studies suggest that exposure to POPs is also a risk factor for HTN. We hypothesized that POPs increase the environmental burden of stroke with comorbid HTN. Methods A population-based study of hospitalization rates for stroke with comorbid HTN in populations presumably exposed to POPs, based on the zip code of residence, was conducted. Data on hospitalizations for stroke with comorbid HTN were obtained from the New York Statewide Planning and Research Cooperative System for 1993-2004. Relative risks, with 95% confidence intervals (RR, 95% CI), of hospitalization were estimated by multiple Poisson regression analysis. Results RR of hospitalization for stroke with comorbid HTN was 13.4% higher in populations residing in zip codes containing or abutting environmental sources of POPs (RR = 1.134; 95% CI, 1.036-1.241; p = 0.006). Also, hospitalization rates were significantly higher in males than in females (RR = 1.397; 95% CI, 1.357-1.437; p < 0.001), in African Americans than in Caucasians (RR = 3.902; 95% CI, 3.617-4.208; p < 0.001), and in older age groups (p for trend < 0.001). These statistically significant findings of the effect of demographic factors are highly consistent with the current knowledge of stroke and serve as indirect quality indicators for our model. Conclusions Results of our study support the hypothesis that exposure to POPs increases the environmental burden of both stroke and HTN.

Introduction It has been noticed many times that schools are buildings with high levels of particulate matter concentrations. Several authors documented that concentrations of particulate matter in indoor school microenvironments exceed limits recommended by WHO namely when school buildings are situated near major roads with high traffic densities. In addition, exercise under conditions of high particulate concentrations may increase the adverse health effects, as the total particle deposition increases in proportion to minute ventilation, and the deposition fraction nearly doubles from rest to intense exercise. Site and methods Mass concentrations of size-segregated aerosol were measured simultaneously in an elementary school gym and an adjacent outdoor site in the central part of Prague by two pairs of collocated aerosol monitors--a fast responding photometer DusTrak and a five stage cascade impactor. To encompass seasonal and annual differences, 89 days of measurements were performed during ten campaigns between 2005 and 2009. Results and discussion The average (all campaigns) outdoor concentration of PM₂.₅ (28.3 μg m⁻³) measured by the cascade impactors was higher than the indoor value (22.3 μg m⁻³) and the corresponding average from the nearest fixed site monitor (23.6 μg m⁻³). Indoor and outdoor PM₂.₅ concentrations exceeded the WHO recommended 24-h limit in 42% and 49% of the days measured, respectively. The correlation coefficient (r) between corresponding outdoor and indoor aerosol sizes increased with decreasing aerodynamic diameter of the collected particles (r = 0.32-0.87), suggesting a higher infiltration rate of fine and quasi-ultrafine particles. Principal component analysis revealed five factors explaining more than 82% of the data variability. The first two factors reflected a close association between outdoor and indoor fine and quasi-ultrafine particles confirming the hypothesis of high infiltration rate of particles from outdoors. The third factor indicated that human activity is the main source of indoor emission of coarse particles. The fourth factor involved only outdoor variables showing the resuspension of coarse ambient aerosol on dry and warm days without its seeming effect on the indoor coarse PM levels. Having in mind that high concentrations of both fine and coarse aerosol were frequently observed in the studied space, our results suggest that indoor exercise in polluted urbanized areas may increase the overall exposure and thus represent a potential health risk to young individuals during physical education at schools.

Introduction In this study, olive tree leaves, collected from 50 sampling sites throughout the Province of Aydın, Turkey, were used to estimate level of pollution by measuring Al, As, B, Ba, Ca, Co, Cr, Cu, Fe, K, Li, Mg, Mn, Na, Ni, Pb, Sr, and Zn concentrations and calculating pollution factor (PF) values. Materials and methods After sample preparation, collected leaves were microwave digested, and extracts were analyzed by an inductively coupled plasma-mass spectrometer. Results and discussion The maximum PF values were ≥10 for a number of elements ranging from 11-13 (Al, As, Cr, Fe, Mn, Ni) to >100 for Cu, Li, and Na. Urban-rural and roadside-nonroadside concentration comparisons showed that some of the elements (As, Cu, and Pb) were at significantly higher levels on urban and/or roadside sampling sites. Summary and conclusion Correlations and factor analysis showed that there may be common sources for some elements, which included several soil types and anthropogenic activities. Based on the results of the statistical source apportionment, possible sources were narrowed down with help of the constructed elemental concentration maps. In conclusion, utilization of olive tree leaves for biomonitoring and assessment of environmental pollution was shown to be possible in the Mediterranean region where they are indigenous and cultivated.

PURPOSE: The aim of this work was to investigate the possibility of using several bush and arboreal plant species, usually present as ornamental plants in street and parks, as environmental indicators of pollution. This is a research paper that evaluates the real possibility of using a fast and low-cost procedure to evaluate the pollution degree through data obtained from plant species growing within an urban environment. METHODS: Leaves of six different bush and arboreal species were collected from different parts of Madrid (Spain), ranging from highly polluted considered areas to medium and low contaminated ones. A total of 66 chemical elements, from major to minor and trace, were determined for every leaf sample by inductively coupled plasma-mass spectrometry. Statistical analyses were carried out using mainly box and whisker plots, linear discriminant analysis and cluster analysis. RESULTS: The pollution by different elements of the studied areas of Madrid cannot be considered generally dangerous for human health. The level detected for the contaminants, in general, is similar or lower than other urban cities. Pb and V concentrations in plant samples tend to increase as traffic density increases. The different studied plant species showed a different capability of accumulation of certain elements. Cedrus deodara accumulates specially Ag, Hg, Mo and V; Cupressus sempervirens, Zr; Pinus pinea, As and Sb; Nerium oleander Ni, Pb, Mo and Se; Ligustrum ovalifolium, Sc and V; and Pittosporum tobira, Ag, Cd, Rb and Sc. CONCLUSIONS: The leaves and needles collected from bush and arboreal plants common in this city have demonstrated to be useful to evaluate the level of pollution not only through the chemical analysis but also through the recognition of the visual injury symptoms. The application of multivariate statistical techniques combined with determining of element concentration and correlation analysis has been proved to be an effective tool for reach the objectives of the present work. This allows visualising quickly the damages and leading the sampling through the points of high-level pollution, saving analysis, time and money.

PURPOSE: Bioaugmentation and biostimulation have been widely applied in the remediation of oil contamination. However, ambiguous results have been reported. It is important to reveal the controlling factors on the field for optimal selection of remediation strategy. In this study, an integrated field landfarming technique was carried out to assess the relative effectiveness of five biological approaches on diesel degradation. The limiting factors during the degradation process were discussed. METHOD: A total of five treatments were tested, including conventional landfarming, nutrient enhancement (NE), biosurfactant addition (BS), bioaugmentation (BA), and combination of bioaugmentation and biosurfactant addition (BAS). The consortium consisted of four diesel-degrading bacteria strains. Rhamnolipid was used as the biosurfactant. The diesel concentration, bacterial population, evolution of CO2, and bacterial community in the soil were periodically measured. RESULTS: The best overall degradation efficiency was achieved by BAS treatment (90 ± 2%), followed by BA (86 ± 2%), NE (84 ± 3%), BS (78 ± 3%), and conventional landfarming (68 ± 3%). In the early stage, the total petroleum hydrocarbon was degraded 10 times faster than the degradation rates measured during the period from day 30 to 100. At the later stage, the degradation rates were similar among treatments. In the conventional landfarming, contaminated soil contained bacteria ready for diesel degradation. CONCLUSION: The availability of hydrocarbon was likely the limiting factor in the beginning of the degradation process. At the later stage, the degradation was likely limited by desorption and mass transfer of hydrocarbon in the soil matrix.

INTRODUCTION: In order to identify a potential surrogate of planktonic ciliate communities for marine bioassessments and evaluating biological conservations, the different taxonomic/numerical resolutions and taxa as surrogates were studied in Jiaozhou Bay, northern China during a 1-year cycle (June 2007–May 2008). MATERIALS AND METHODS: Samples were collected biweekly from a depth of 1 m at each of five sites. A range of physicochemical parameters were also measured in order to determine water quality. RESULTS: The genus- and family-level resolutions maintained sufficient information to evaluate the ecological patterns of the ciliate communities in response to environmental status. The non-loricate oligotrichous ciliate assemblages in both abundance and occurrence may be used as a surrogate of planktonic ciliate communities. Heavy data transformations were an optimal strategy for the species level of planktonic ciliates, while mild data transformations were for the higher. The ordination patterns based on species biomass, occurrence, and biomass/abundance ratio matrices were significantly consistent with that of species abundance data. CONCLUSION: The results suggest that the use of simplifications at both taxonomic and numerical resolutions are time-efficient and would allow improving sampling strategies of large spatial/temporal scale monitoring programs and biological conservation researches in the marine ecosystem with a relative paucity of scientists.

Purpose α-Hexachlorocyclohexane (HCH), β-HCH, and lindane (γ-HCH) were listed as persistent organic pollutants by the Stockholm Convention in 2009 and hence must be phased out and their wastes/stockpiles eliminated. At the last operating lindane manufacturing unit, we conducted a preliminary evaluation of HCH contamination levels in soil and water samples collected around the production area and the vicinity of a major dumpsite to inform the design of processes for an appropriate implementation of the Convention. Methods Soil and water samples on and around the production site and a major waste dumpsite were measured for HCH levels. Results All soil samples taken at the lindane production facility and dumpsite and in their vicinity were contaminated with an isomer pattern characteristic of HCH production waste. At the dumpsite surface samples contained up to 450 g kg⁻¹ Σ HCH suggesting that the waste HCH isomers were simply dumped at this location. Ground water in the vicinity and river water was found to be contaminated with 0.2 to 0.4 mg l⁻¹ of HCH waste isomers. The total quantity of deposited HCH wastes from the lindane production unit was estimated at between 36,000 and 54,000 t. Conclusions The contamination levels in ground and river water suggest significant run-off from the dumped HCH wastes and contamination of drinking water resources. The extent of dumping urgently needs to be assessed regarding the risks to human and ecosystem health. A plan for securing the waste isomers needs to be developed and implemented together with a plan for their final elimination. As part of the assessment, any polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/PCDF) generated during HCH recycling operations need to be monitored.

INTRODUCTION: This study aimed to analyze antioxidant responses and oxidative damage induced by two inorganic forms of arsenic (As; AsIII and AsV) in an estuarine polychaete species, Laeonereis acuta (Nereididae). The capacity of arsenic biotransformation was also evaluated through the methylation process considering the activity of a key enzyme involved in the metabolization process. MATERIALS AND METHODS: Worms were exposed to 50 μg (AsIII or AsV)/l during 2 or 7 days, plus a control group. Endpoints analyzed included concentration of reactive oxygen species (ROS), activities of antioxidant enzymes such as glutathione reductase (GR), total glutathione-S-transferase (GST), and omega isoform (GST Ω), glucose-6-phosphate deshydrogenase (G6PDH), levels of the antioxidant glutathione (GSH), and lipid peroxides concentration (TBARS). RESULTS AND DISCUSSION: Results showed: (1) GR inhibition after 2-day exposure to both As forms (p < 0.05); (2) GST Ω inhibition after 7-day exposure to AsIII paralleled by an increase in total GST activity (p < 0.05); (3) augmented G6PDH activity after 7-day exposure to both As forms (p < 0.05); (4) no differences in terms of ROS and TBARS; and (5) inhibition of GST Ω activity in AsIII exposed worms, which was concomitant with a lowering of mono- and dymethylated arsenic species. CONCLUSION: These results confirm the reactivity of some biochemical variables of L. acuta to As and indicates its importance as a sentinel species in estuarine regions with presence of arsenic.

Background Environmental agencies have to take measures to either reduce discharges and emissions of nitrate or to remediate nitrate-polluted water bodies where the nitrate concentrations exceed threshold values. Isotope data can support the identification of nitrate pollution sources and natural attenuation processes of nitrate. Review This review article gives an overview of the information available to date regarding nitrate source apportionment in surface waters with the ambition to help improving future studies. Different isotope approaches in combination with physicochemical and hydrological data can successfully be used in source apportionment studies. A sampling strategy needs to be developed based on possible nitrate sources, hydrology and land use. Transformations, transport and mixing processes should also be considered as they can change the isotope composition of the original nitrate source. Conclusion Nitrate isotope data interpreted in combination with hydrological and chemical data provide valuable information on the nitrate pollution sources and on the processes nitrate has undergone during its retention and transport in the watershed. This information is useful for the development of an appropriate water management policy.

Introduction Inorganic ion concentrations in event-based wet-only precipitation samples collected during the south-west (SW) monsoon at an urban location in Western India, Ahmedabad between July 2000 and September 2002 were measured by Rastogi and Sarin (2007). Methods For the first time at a location in India, an advanced factor analysis model was retrospectively applied to the measured concentrations of ions (Rastogi and Sarin 2007) in precipitation for source apportionment. Positive matrix factorization resolved five factors, including crustal material, sea salt, nitrate/sulfate-rich factor, ammonium-rich factor, and free acidity. Results and discussion Amongst the model-resolved factors, crustal material was the highest contributor to the total dissolved solids (TDS) accounting for 44.1% on average. Potential source contribution function (PSCF) analysis identified source locations along the eastern coast of Somalia, Yemen, Oman, and the United Arab Emirates for this factor. Sea salt was the second highest contributor accounting for 29.8%. The potential source regions of this factor were also identified in the Arabian Sea and the southern Indian Ocean along the coast of Africa, and the Arabian Gulf. This study also examined the spatial relationships between the source locations of chemical species in precipitation and in ambient aerosol (resolved in an earlier study). Conclusions Crustal material was the highest contributor to TDS at the study location. Spatial relationships between aerosol and precipitation factor source regions suggested that below-cloud scavenging of aerosol particles was a likely contributor to the chemical species apportioned to various precipitation factors. Additionally, source types of chemical species in precipitation resolved in this study were qualitatively compared with those identified at other locations in India. The comparison showed that soil was an important contributor to the dissolved mass of chemical species in precipitation at all locations in India.