The potential impacts of sea level rise along the coastal zone of Kanyakumari District in Tamilnadu,India

Climate change associated with sea level rise (SLR) is one of the major environmental concerns of today. This paper presents an assessment of the impacts of sea level rise on the coastal zone of Kanyakumari District in Tamilnadu, India. Digital Elevation Model (DEM) combined with overlay techniques in GIS are used in determining the inundation zones along the coastal region. The analysis evaluated the impact on coastal fishing villages, landuse, tourist spots and sensitive areas under threat. The vulnerability of the coastal areas in Kanyakumari to inundation was quantified, based on the projected sea level rise scenarios of 0.5 and 1 m. Our findings reveal that approximately 13 km² of the land area of Kanyakumari would be permanently inundated due to SLR. This would result in loss of land, alteration of the coastal zone and affects coastal ecosystem. From the study, the mitigation measures (engineering measures) and Coastal Zone Management practices that can be taken to protect human life and property from sea level rise are suggested.     

Analytical survey of arsenic in geothermal waters from sites in Kyushu,Japan, and a method for removing arsenic using magnetite

The objective of this study was to survey the cation and anion contents of geothermal waters to gather fundamental information on geographical variations. Sixteen sites in hot spring areas on the island of Kyushu in Japan were studied. The study focused on the arsenic content of the samples. Very high arsenic concentrations (more than 0.1 mg/l) were detected in most of the geothermal waters sampled. High contents of boron and fluoride (more than 1.0 mg/l) were also detected in some samples. Arsenic removal was performed on a laboratory scale using columns packed with a magnetite-type adsorbent. The reduction of arsenic contamination to a concentration of less than 0.01 mg/l could be achieved in the early stages of adsorption (bed volume = 200).     

Anthropogenic influence on surface water quality of the Nhue and Day sub-river systems in Vietnam

In order to investigate the temporal and spatial variations of 14 physical and chemical surface water parameters in the Nhue and Day sub-river systems of Vietnam, surface water samples were taken from 43 sampling sites during the dry and rainy seasons in 2007. The results were statistically examined by Mann–Whitney U-test and hierarchical cluster analysis. The results show that water quality of the Day River was significantly improved during the rainy season while this was not the case of the Nhue River. However, the river water did not meet the Vietnamese surface water quality standards for dissolved oxygen (DO), biological oxygen demand (BOD₅), chemical oxygen demand (COD), nutrients, total coliform, and fecal coliform. This implies that the health of local communities using untreated river water for drinking purposes as well as irrigation of vegetables may be at risk. Forty-three sampling sites were grouped into four main clusters on the basis of water quality characteristics with particular reference to geographic location and land use and revealed the contamination levels from anthropogenic sources.     

Biosecurity threats: the design of surveillance systems,based on power and risk

We consider the problem of designing a surveillance system to detect a broad range of invasive species across a heterogeneous sampling frame. We present a model to detect a range of invertebrate invasives whilst addressing the challenges of multiple data sources, stratifying for differential risk, managing labour costs and providing sufficient power of detection. We determine the number of detection devices required and their allocation across the landscape within limiting resource constraints. The resulting plan will lead to reduced financial and ecological costs and an optimal surveillance system.     

Increasing polybrominated diphenyl ether (PBDE) contamination in sediment cores from the inner Clyde Estuary,UK

The concentrations of 16 polybrominated diphenyl ether (PBDE) congeners in six short sediment cores from the Clyde Estuary were determined by gas-chromatography mass-spectrometry. Total PBDE concentrations ranged from 1 to 2,645 μg/kg and the average concentration was 287 μg/kg. BDE-209 was the main congener and varied from 1 to 2,337 μg/kg. Elevated total PBDE concentrations were observed close to the sediment surface in the uppermost 10 cm of four of the six sediment cores. Comparison of the down core PBDE profiles revealed that the increase was driven by the accumulation of deca-BDE. Although the deca-BDE mix was dominant, the presence of lower molecular weight congeners BDE-47, BDE-99, BDE-183 and BDE-153 at most sediment intervals suggested additional sources of penta-BDE and octa-BDE pollution. Changing PBDE source input was the major factor in influencing the proportion of nona-brominated congeners, although other explanations such as post burial photo-debromination of BDE-209 cannot be entirely discounted. A clear cascading to lower hepta-, hexa-, and penta-homologues was not found. The increase in total PBDE concentrations and particularly the deca-BDE may possibly be ascribed to the use and subsequent disposal of electrical appliances such as televisions and computers. In the Clyde sediments, the proportion of nona-brominated congeners was higher than that reported for commercial mixtures. This might be due to changing sources of PBDEs or post burial photo-debromination of BDE-209.     

Changes in chemical forms of lead in temperate and semiarid soils in sterile and unsterile conditions

Sequential extraction has been used as a suitable method for fractionation of chemical forms of trace elements and study of their plant availability. Surface soils were sampled from Guilan and Hamadan provinces in north and northwest of Iran with temperate and semiarid climates. The chemical forms of Pb in the Pb(NO₃)₂-treated (400 μg Pb g⁻¹) soils have been studied in solid state incubation (FC) at 27°C in sterile and unsterile conditions. After 20 min and 3600 h a sequential extraction scheme was also used to fractionate Pb of incubated samples into soluble-exchangeable (Sol-Exch), carbonates associated (ACar), organic matter associated (AOM), Mn oxide associated (AMnOx), Fe oxide associated (AFeOx), and residual (Res) forms. Temperate soil samples had higher clay content, cation exchange capacity (CEC), dichromate oxidable organic carbon (OC), total Kjeldahl-nitrogen (TN), biological activity, amorphous and crystalline Fe and Al, but semiarid soil samples had higher sand content, pH, equivalent calcium carbonate (ECC), available P and K. Soil lead fractionation revealed that in both groups of soils Pb largely changed to exchangeable, carbonates associated and organic associated forms after 20 min. The chemical forms of Pb differed widely among soils after 3600-h incubation. The conversion rate of Pb from more available forms to less available forms was higher in temperate soils with higher Fe–Mn oxides and OM contents compared to semiarid soils. In temperate soils after 3600-h incubation, greater content of Pb was observed in Res (68%), AOM (14%), ACar (7%), and AMnOx (5%) fractions. However, in semiarid soils greater content of Pb was observed in Res (61%), ACar (16%), Sol-Exch (8%), and AOM (8%) fractions. The sum of AMnOx and AFeOx chemical forms for Pb in semiarid soils compared to temperate soils was lower. It was only 7% against 9% in temperate soils. Soil microorganisms in unsterile soils had significant effect on AOM, AFeOx and Res fractions of Pb. They not only increased AOM and AFeOx fractions of Pb in soils but also decreased Res fraction of Pb significantly.     

Distribution and availability of potentially toxic metals in soil in central area of Belgrade,Serbia

Belgrade, capital city of Serbia, has over 1,600,000 inhabitants and over 400,000 vehicles trafficking every day on its streets. The investigation of soil pollution was performed by sequential extraction analysis to investigate the availability of potentially toxic metals (Zn, Cd, Pb, Co, Ni, Cu, Cr and Mn) under different oxidation and pH conditions. All investigated metals were mainly extracted from soils with neutral or acidic extractants. Serious pollution was observed along roads and streets with high traffic frequency, but Pb and Ni pollution was the highest since their concentrations exceed both soil Serbian standard and Canadian guidance values and is characteristic for all investigated sites. Cd, Cu, Cr and Zn concentrations are moderately high since they are between Canadian guideline and Serbian standard.     

Photochemical reaction of nitro-polycyclic aromatic hydrocarbons: effect by solvent and structure

Photochemical degradation of 1-nitropyrene, 2-nitrofluorene, 2,7-dinitrofluorene, 6-nitrochrysene, 3-nitrofluoranthene, 5-nitroacenaphthene, and 9-nitroanthracene was examined in CHCl₃, CH₂Cl₂, DMF, DMF/H₂O (80/20), CH₃CN, or CH₃CN/H₂O (80/20). The degradation mostly follows the first order kinetics; but a few follow second order kinetics or undergo self-catalysis. The photodegradation rates follow the order: CHCl₃ > CH₂Cl₂ > DMF > DMF/H₂O > CH₃CN > CH₃CN/H₂O. DMF is an exceptional solvent because three of the seven compounds undergo self-catalytic reaction. 9-Nitroanthracene, which has a perpendicular nitro group, is the fastest, while the more compact 1-nitropyrene and 3-nitrofluoranthene are the slowest degrading compounds.     

Quantification of singlet oxygen and hydroxyl radicals upon UV irradiation of surface water

We measured the formation rate and the steady-state concentration of hydroxyl radicals and of singlet oxygen upon irradiation of lake water. There is controversy about the importance of singlet oxygen in the environmental photochemistry, but here we show that the steady-state concentration of ¹O₂ under irradiation can be higher by about two orders of magnitude compared to the hydroxyl radical. The higher occurrence of singlet oxygen in surface waters is mainly due to a higher rate of formation, because the transformation rate constants of ¹O₂ (collision with the solvent) and of ^·OH (reaction with dissolved compounds) are comparable.