Assessment of groundwater vulnerability to pollution in Dire Dawa,Ethiopia using DRASTIC

Assessment of groundwater vulnerability to pollution is an effective tool for the delineation of groundwater protection zones. DRASTIC approach was used to determine vulnerability zones in Dire Dawa groundwater basin, a semiarid region of Ethiopia. Maps of the seven DRASTIC parameters were prepared. GIS-ArcView was used for mapping and performing weighted-overlay analysis. The result of the analysis indicated that eastern part of the study area, in which Dire Dawa town is located, is highly vulnerable. A low aquifer vulnerability class was determined for the western portion of the study area as a result of greater groundwater depths, higher relative soil-clay content, and relatively low recharge rates for this area. The area between the two zones is of medium vulnerability. Observed nitrate concentrations in boreholes are in accordance with the vulnerability map. Some of the boreholes in the Sabian well field (Dire Dawa area) already deliver groundwater with nitrate levels significantly exceeding health standards set by the World Health Organization, while boreholes in the western part (low vulnerability zone) contain almost no nitrate. The result of this study is useful for risk assessments and for the development of effective groundwater management strategies for this region and others like it.     

Contamination risk assessment of fresh groundwater using the distribution and chemical speciation of some potentially toxic elements in Calabar (southern Nigeria)

The computer program PHREEQC was used to determined the distribution, chemical speciation and mineral saturation indices in a fresh groundwater environment with limited mining activities in the adjoining areas. The aim was mainly to determine the potential risk of a coastal plain aquifer contamination by some potentially toxic elements. The results show that the elements Ba, Cd, Cu, Fe, Mn, Ni, Rb, Sr, and Zn are distributed as free metal ions. Arsenic is in the neutral form of H₃AsO₃ ^o, while three species of aluminium [Al³⁺, AlOH₂, Al(OH)₂ ⁺] dominate. The major species of uranium include UO₂CO₃, UO₂²⁺+, UO₂⁺, and UO₂OH⁺, respectively, in order of abundance. The groundwater is saturated with respect to alunite [KAl₃ (SO₄)₂ (OH)₆], basaluminite [Al₄ (OH)₁₀ SO₄], boehmite [Al(OH)], Cu metal (Cu), cuprous ferrite (CuFeO₂), diaspore [AlO(OH)], gibbsite [Al(OH)₃], goethite (FeOOH), hematite (Fe₂O₃), magnetite (Fe₃O₄) and uraninite (UO₂). Most of the species are not mobile under the prevailing pH (3.3 to 5.9) and Eh (7 to 158 mV) conditions. The mobile ones are very low in concentration and will be immobilized by precipitation of mineral phases. The study concludes that presently these species do not pose any risk to the aquifer.     

Hydrochemical evolution and arsenic release in shallow aquifer in the Titas Upazila,Eastern Bangladesh

Groundwater arsenic (As) concentrations above 10 μg/L (World Health Organization; WHO standard) are frequently found in the Titas Upazila in Bangladesh. This paper evaluates the groundwater chemistry and the mechanisms of As release acting in an underground aquifer in the middle-northeast part of the Titas Upazila in Bangladesh. Previous measurements and analyses of 43 groundwater samples from the region of interest (ROI) are used. Investigation is based on major ions and important trace elements, including total As and Fe in groundwater samples from shallow (8–36 m below ground level: mbgl) and deep (85–295 mbgl) tube wells in the aforementioned ROI. Principal hydrochemical facies are Ca–HCO₃, with circumneutral pH. The different redox-sensitive constituents (e.g., As, Fe, Mn, NH₄, and SO₄) indicate overlapping redox zones, leading to differences regarding the redox equilibrium. Multivariate statistical analysis (factor analysis) was applied to reduce 20 chemical variables to four factors but still explain 81% of the total variance. The component loadings give hints as to the natural processes in the shallow aquifers, in which organic matter is a key reactant. The observed chemistry of As, Fe, and Mn can be explained by simultaneous equilibrium between Fe-oxide and SO₄ reduction and an equilibrium of rhodochrosite precipitation/dissolution. A correlation test indicates the likeliness of As release by the reductive dissolution of Fe-oxides driven by the degradation of sediments organic matter. Other mechanisms could play a role in As release, albeit to a lesser extent. Reactive transport modeling using PHREEQC reproduced the observed chemistry evolution using simultaneous equilibrium between Fe-oxide and SO₄ reduction and the equilibrium of rhodochrosite dissolution/precipitation alongside organic matter oxidation.     

Anwendung eines neuen Feldanalysenverfahrens zur Untersuchung der Stabilität von Arsen und seinen anorganischen Spezies in aquatischen Systemen

Using of a New Field Analysis Method to Investigate the Stability of Arsenic and its Inorganic Species in Aquatic Systems The stability of arsenic species in aquatic systems is limited by the possibilities of chemical and biochemical reactions. Redox reactions and bioalkylation lead to changes of the species ratios. In this work, the stability of As(III) and As(V) was examined at storage of distilled, de-ionized, and drinking water at different conditions (refrigerator/room temperature; daylight/darkness) and additions (sulfuric acid; ascorbic acid). The determination of these species was carried out by a modified spectrophotometric method, suitable for laboratory analysis as well as for field analysis. The results show that chemical oxidation and biochemical reduction can occur. Sulfuric acid is favourable for the stabilization of total arsenic and of the inorganic species.     

Light-induced bird strikes on vessels in Southwest Greenland

Light-induced bird strikes are known to occur when vessels navigate during darkness in icy waters using powerful searchlight. In Southwest Greenland, which is important internationally for wintering seabirds, we collected reports of incidents of bird strikes over 2-3 winters (2006-2009) from navy vessels, cargo vessels and trawlers (total n = 19). Forty-one incidents were reported: mainly close to land (<4 km, 78%), but one as far offshore as 205 km. Up to 88 birds were reported killed in a single incident. All occurred between 5 p.m. and 6 a.m. and significantly more birds were involved when visibility was poor (snow) rather than moderate or good. Among five seabird species reported, the common eider (Somateria mollissima) accounted for 95% of the bird casualties. Based on spatial analyses of data on vessel traffic intensity and common eider density we are able to predict areas with high risk of bird strikes in Southwest Greenland.     

Comparison of polar mesospheric cloud measurements from the Cloud Imaging and Particle Size experiment and the solar backscatter ultraviolet instrument in 2007

We compare measurements from the Aeronomy of Ice in the Mesosphere (AIM) Cloud Imaging and Particle Size (CIPS) experiment to the NOAA-17 solar backscatter ultraviolet (SBUV/2) instrument during the 2007 Northern Hemisphere polar mesospheric cloud (PMC) season. Daily average Rayleigh scattering albedos determined from identical footprints from the CIPS nadir camera and SBUV/2 agree to better than ～5% throughout the season. Average PMC brightness values derived from the two instruments agree to within ±10%. PMC occurrence frequencies are on average ～5% to nearly a factor of two higher in CIPS, depending on latitude. Agreement is best at high latitudes where clouds are brighter and more frequent. The comparisons indicate that AIM CIPS data are valid for scientific analyses. They also show that CIPS measurements can be linked to the long time series of SBUV/2 data to investigate long-term variability in PMCs.     

Sorption of uranium(VI) at the clay mineral–water interface

Batch experiments were conducted to study the sorption of uranium on selected clay minerals (KGa-1b and KGa-2 reference kaolinite, SWy-2 and STx-1b reference montmorillonite, and IBECO natural bentonite) as a function of pH (4–9) and 0.001, 0.01, and 0.025 M NaCl in equilibrium with the CO₂ partial pressure of the atmosphere. Uranium concentrations were kept below 100 μg L⁻¹ to avoid precipitation of amorphous Uranium-hydroxides. Solely PTFE containers and materials were used, because experiments showed significant sorption at higher pH on glass ware. All batch experiments were performed over a period of 24 h, since kinetic experiments proved that the common 10 or 15 min are in many cases by far not sufficient to reach equilibrium. Kaolinite showed much greater uranium sorption than the other clay minerals due to the more aluminol sites available. Sorption on the poorly crystallized KGa-2 was higher than on the well-crystallized KGa-1b. Uranium sorption on STx-1b and IBECO exhibited parabolic behavior with a sorption maximum around pH 6.5. Sorption of uranium on montmorillonites showed a distinct dependency on sodium concentrations because of the effective competition between uranyl and sodium ions, whereas less significant differences in sorption were found for kaolinite. The presence of anatase as impurity in kaolinite enhanced the binding of uranyl-carbonate complexes with surface sites. The kinetic of uranium sorption behavior was primarily dependent on the clay minerals and pH. A multisite surface complexation model without assuming exchange is based on the binding of the most dominant uranium species to aluminol and silanol edge sites of montmorillonite, respectively to aluminol and titanol surface sites of kaolinite. For eight surface species, the log_k was determined from the experimental data using the parameter estimation code PEST together with PHREEQC.