Dissolved Nutrient Distributions in Groundwater in the Mediterranean Coastal Plains – the Case of Silifke,Turkey

Total carbon, nitrogen, and phosphate parameters were studied for the first time in the groundwater in the Silifke coastal plain, which is a RAMSAR site in Turkey. Seasonal variations of these parameters in the plain were examined based on groundwater data collected from 21 wells during the winter, spring, summer, and fall seasons. Total dissolved organic carbon (DOC), inorganic carbon (DIC), inorganic phosphate (DIP), inorganic nitrogen (DIN), and total alkalinity (TAlk) average values in the groundwater were low in all seasons (<2.2 mg/L for DOC; <54 mg/L for DIC; <0.06 mg/L for DIP; <1.5 mg/L for DIN; <232 mg/L for TAlk). The results showed a strong relationship between DIC and as expected. The results indicate that the content of these parameters in the groundwater of Silifke coastal plain pose no or little risk at present. However, computed Langelier Saturation Index (LSI) values indicated that the groundwater has a tendency to form scale and CaCO₃ precipitation may occur.     

Trace elements in tissues of cetacean species rarely stranded along the Israeli Mediterranean coast

In this paper we present the concentrations of Hg, Cd, Se, Pb, Cu, Mn, Zn and Fe in organs of 6 non-common specimens of cetaceans that were stranded along the Israeli Mediterranean coast (IMC), during 2002–2010: two fin whales, one minke whale, one Cuvier’s beaked whale, one rough-toothed dolphin, and one Risso’s dolphin. Most of the specimens were calves stranded by accident. Concentrations of Hg and Cd were low in tissues of the baleen whales and higher in the toothed whales, with maximum concentrations of 1067 mg kg⁻¹ Hg in the liver of the Risso’s dolphin and 29 mg kg⁻¹ Cd in the kidney of the Cuvier’s beaked whale. As far as we are aware, this is the first report of trace elements in baleen whales in the Eastern Mediterranean, and the first report of trace elements in minke whale and rough-toothed dolphin in the Mediterranean.     

The location of deep salinity sources in the Israeli Coastal aquifer

The salinization process of the Israeli Coastal aquifer has led to an average concentration of about 200 mgCl/l with a significant number of discrete salinity plumes in the middle and southern regions. The salinity of these plumes is high (500–1000 mgCl/l) and is increasing rapidly. Geochemical evidence has suggested that the salinity source in the Be'er Tuvia plume (in the south part of the aquifer) is at the bottom of the aquifer. This paper describes a solution of the source inverse problem and its application in the Be'er Tuvia plume. A transient two-dimensional finite element model was solved and the source terms were computed at each node in a 14×14 km² area. An error analysis has shown that when no errors are introduced in the input data the reconstruction is perfect. The results of a sensitivity analysis are presented and the actual reconstruction errors are estimated. Applying the model in the Be'er Tuvia region indicates that a salinity source exists about 1 km to the west and 1.5 km to the north of the center of the salinity plume. This source is believed to be the plume source.     

Trace element content of seagrasses in the Leschenault Estuary,Western Australia

Estuarine environments are particularly vulnerable to human impacts. In this study, trace elements in Ruppia megacarpa, Halophila ovalis, sediment and porewater were analysed to assess the potential contamination of the Leschenault Estuary, Western Australia, from a primarily agricultural drain. Sediment concentrations of Cd, Cu, Mn, and Ni and were highest nearest the drain while Al, As, Cr, Fe and Zn and were highest further from the drain. H. ovalis showed greater accumulation of Fe, Al, and As than R. megacarpa. Concentrations of Fe, Al, As, and Ni were generally higher in below-ground plant parts than above, suggesting uptake of these trace elements via the sediment-route pathway. This study suggested that the drain was a source of Cu and Mn, with these elements entering the estuary through water inflows. As and Fe, were highest furthest from the drain suggesting input of trace elements from sources other than the drain under study.     

The Analytic Element Method for rectangular gridded domains,benchmark comparisons and application to the High Plains Aquifer

Groundwater studies face computational limitations when providing local detail (such as well drawdown) within regional models. We adapt the Analytic Element Method (AEM) to extend separation of variable solutions for a rectangle to domains composed of multiple interconnected rectangular elements. Each rectangle contains a series solution that satisfies the governing equations and coefficients are adjusted to match boundary conditions at the edge of the domain and continuity conditions across adjacent rectangles. A complete mathematical implementation is presented including matrices to solve boundary and continuity conditions. This approach gathers the mathematical functions associated with head and velocity within a small set of functions for each rectangle, enabling fast computation of these variables. Benchmark studies verify that conservation of mass and energy conditions are accurately satisfied using a method of images solution, and also develop a solution for heterogeneous hydraulic conductivity with log normal distribution. A case study illustrates that the methods are capable of modeling local detail within a large-scale regional model of the High Plains Aquifer in the central USA and reports the numerical costs associated with increasing resolution, where use is made of GIS datasets for thousands of rectangular elements each with unique geologic and hydrologic properties, Methods are applicable to interconnected rectangular domains in other fields of study such as heat conduction, electrical conduction, and unsaturated groundwater flow.     

Trace Metals in Selected Benthic Invertebrates from Belgian Coastal Waters (1981–1996)

Mercury, cadmium, lead, copper, zinc and chromium were assessed in brown shrimp (Crangon crangon), swimming crab (Liocarcinus holsatus), hermit crab (Pagurus bernhardus), starfish (Asterias rubens) and cut trough shell (Spisula subtruncata) from ten sampling stations off the Belgian coast, including three dredge spoils disposal sites. Calculations of time trends indicated that on the whole concentrations of trace metals had significantly decreased since 1981, also on dredged material dumping sites. Starfish and hermit crab were found to be the most promising benthic indicator species for metal contamination. Globally, the location of the sites, including the dredge spoils disposal zones, showed to be of little influence on the concentrations of trace metals.     

A Multi‐Element Ion‐Pair Extraction for Trace Metals Determination in Environmental Samples

A multi‐element ion‐pair extraction method was described for the preconcentration of Cd(II), Co(II), Cr(III), Cu(II), Fe(III), Mn(II), Ni(II), Pb(II), and Zn(II) ions in environmental samples prior to their determinations by flame atomic absorption spectrometry (FAAS). As an ion‐pair ligand 2‐(4‐methoxybenzoyl)‐N′‐benzylidene‐3‐(4‐methoxyphenyl)‐3‐oxo‐N‐phenyl‐propono hydrazide (MBMP) was used. Some analytical parameters such as pH of sample solution, amount of MBMP, shaking time, sample volume, and type of counter ion were investigated to establish optimum experimental conditions. No interferences due to major components and some metal ions of the samples were observed. The detection limits of the proposed method were found in the range of 0.33–0.9 µg L^?1 for the analyte ions. Recoveries were found to be higher than 95% and the relative standard deviation (RSD) was less than 4%. The accuracy of the procedure was estimated by analyzing the two certified reference materials, LGC6019 river water and RTC‐CRM044 soil. The developed method was applied to several matrices such as water, hair, and food samples.     

Extended Sediment Quality Rating for Trace Elements in Urban Waters – Case Study Klinke,Germany

The European Water Framework Directive (WFD) commits European Union member states to achieving good ecological status in all water bodies by 2015. For sediments the definition of good chemical status is based on numerical sediment quality guidelines. The aqua regia fraction is thus used for the evaluation of heavy metal concentrations in sediments. The chemical constituents in sediments responsible for mobility and toxicity are not considered generally. This article presents the combining of the sequential BCR procedure, for determining the chemical species of relevant elements, with the geoaccumulation index principle a numerical classification method for sediment quality guidelines. Using the BCR method it can be demonstrated that changes in element speciation can lead to more highly mobile species of trace elements which may affect the hazardous potential of sediments despite the “good chemical status” classification for aqua regia digestions. The Klinke stream is an urban surface water body located in Magdeburg, the state capital of Saxony‐Anhalt, Germany. Using this stream as an example it is shown that this additional information helps to describe the dynamics and discharge of the trace elements Al, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Rb, Sr, Mo, Pd, Cd, Sb, Ba, Pb, Bi, and U into the Elbe River from urban water bodies.     

Role of Nitrogen Oxides,Black Carbon,and Meteorological Parameters on the Variation of Surface Ozone Levels at a Tropical Urban Site – Hyderabad,India

In this study, temporal variations of surface ozone (O₃) were investigated at tropical urban site of Hyderabad during the year 2009. O₃, oxides of nitrogen (NO_x = NO + NO₂), black carbon (BC), and meteorological parameters were continuously monitored at the established air monitoring station. Results revealed the production of surface O₃ from NO₂ through photochemical oxidation. Averaged datasets illustrated the variations in ground‐level concentrations of these air pollutants along different time scales. Maximum mean concentrations of O₃ (56.75 ppbv) and NO_x (8.9 ppbv) were observed in summer. Diurnal‐seasonal changes in surface O₃ and NO_x concentrations were explicated with complex atmospheric chemistry, boundary layer dynamics, and local meteorology. In addition, nocturnal chemistry of NO_x played a decisive role in the formation of O₃ during day time. Mean BC mass concentration in winter (10.92 µg m^?3) was high during morning hours. Heterogeneous chemistry of BC on O₃ destruction and NO_x formation was elucidated. Apart from these local observations, long‐range transport of trace gases and BC aerosols were evidenced from air mass back trajectories. Further, statistical modeling was performed to predict O₃ using multi‐linear regression method, which resulted in 91% of the overall variance.     

Treatment of Groundwater Containing Methane – Combination of the Processing Stages Desorption and Filtration

Methane is produced under anaerobic conditions by metabolic processes in microbes and can occur in waters of the types anoxic‐anaerobic (RG 1/2) and anaerobic‐reduced (RG 2). If the concentration of methane lies below 0.2 mg/L, then no special treatment processes are required apart from dosing of oxygen and rapid sand filtration, which are performed to remove iron, manganese, and ammonium. The research results show that a higher concentration of methane must be specially treated. From the point of view of stable deferrisation, oxidation of up to 2 mg/L is tolerable in rapid sand filtration. However, an unusual increase in regrowth potential was observed. For this reason, the oxidation of methane should be reduced to 0.5 mg/L until further experiments yield results on the microbiological stability of treated water. Rapid sand filters for nitrification and demanganisation should have a maximum methane loading of 0.2 mg/L. The experiments show that nitrification first occurs at a methane concentration below 0.1 mg/L. During the working in of demanganisation, the inlet water should be free of methane. Therefore desorption is often required. If there is less than 1 mg/L to be degassed, then desorption can be achieved with overpressure in the oxidiser without any change in the carbonate‐bicarbonate equilibrium. With other systems, such as packed columns, wetted‐wall columns, or percolators, carbon dioxide is removed simultaneously. By means of the coefficients of similarity found, it was shown that methane and carbon dioxide desorb in different proportions depending on the system, and that the discharge of carbon dioxide can be reduced through a decrease in the air/water ratio.     

Trace elements in alluvia of the upper Vistula as indicators of palaeohydrology

In the Vistula valley near Góra, at the northern foreland of the Carpathians Mountains, there are young alluvia deposited in the historical period. These alluvia are difficult to date precisely because of the lack of organic interbedded material. In the Vistula drainage basin upstream of Góra since the second half of 18th century small centres of metal, textile, motor, and petrochemical industries have been developed. Concentrations of trace elements such as: Cr, Mn, Co, Ni, Cu, Zn, Cd, Pb, and of some macroelements were used as indicators of the age of different alluvial fills. The main part of the Vistula valley floor was built up by sediment accumulation before the development of industry but after the medieval phase of rural colonization of the Carpathians. Deposits filling the abandoned channels dissecting the valley floor have an increased content of some trace elements and deposits date from the second half of the 18th century, when the first foundries and blacksmith's shops were developed. A drastic increase of concentration of the most abundant trace elements in the youngest alluvial fill indicates that the fill dates from the last decade of rapid industrial development.     

Temporal Variability of Major and Trace Element Concentrations in the Groundwaters of Mt. Etna (Italy): Effects of Transient Input of Magmatic Fluids Highlighted by Means of Cluster Analysis

Data for major, minor and trace elements in groundwaters from Mt. Etna volcano collected in 1994, 1995 and 1997 were analyzed using Cluster Analysis (CA). Two groups of sampling sites were identified (named clusters A and B), mainly on the basis of their different salinity and content of dissolved CO₂. The highest levels of both of these parameters were observed in the sites of cluster A, located in the lower south-western and central eastern flanks of the volcano. For both of the statistical groups CA was repeated, taking into account the mean values of each parameter in time, and the results allowed us to recognize four distinct groups of parameters for each group of sites on the basis of their temporal patterns. Four different types of temporal patterns were recognized: concave, convex, increasing, decreasing. The observed changes were basically interpreted as a result of the different response of dissolved chemical elements to changes in the aqueous environment and/or in their solubility/mobility in water due to different rates of input of magmatic gases to Etna’s aquifers. The main changes occurred in 1995, when Etna’s volcanic activity resumed after a two-year period of rest. The temporal changes of the majority of the studied parameters (water temperature, water conductivity, Eh, pH, Al, Mg, B, Ca, Cl⁻, Hg, Mn, Mo, Na, Ni, Se, Si, Sr, Cr Zn and pCO₂) were not cluster-dependent, therefore they were not apparently affected by differences in water salinity between the two groups of sampling sites. A limited number of parameters (Ti, K, Li, HCO₃⁻, As, Fe, SO₄²⁻, Cu and V), however, manifested different behaviors, depending on the cluster of sites to which they belonged, thus suggesting their apparent dependency on water salinity.     

Determination of Trace Levels of Nickel and Manganese in Soil,Vegetable, and Water

A simple and reliable method for rapid and selective extraction and determination of trace levels of Ni²⁺ and Mn²⁺ was developed by ionic liquid (IL) based dispersive liquid–liquid microextraction coupled to flame atomic absorption spectrometry (FAAS) detection. The proposed method was successfully applied to the preconcentration and determination of nickel and manganese in soil, vegetable, and water samples. After preconcentration, the settled IL‐phase was dissolved in 100 µL of ethanol and aspirated into the FAAS using a home‐made microsample introduction system. Injection of 50 µL of each analyte into an air–acetylene flame provided very sensitive spike‐like and reproducible signals. Effective parameters such as pH, amount of IL, volume of the disperser solvent, concentration of the chelating agent, and effect of salt concentration were inspected by a (2^5‐1) fractional factorial design to identify the most important parameters and their interactions. Under optimum conditions, preconcentration of 10 mL sample solution permitted the detection of 0.93 µg L^?1 Ni²⁺ and 0.52 µg L^?1 Mn²⁺ with enrichment factors 77.2 and 82.6 for Ni²⁺ and Mn²⁺, respectively. The accuracy of the procedure was evaluated by analysis of a certified reference material (CRM TMDW‐500, drinking water).     

Trace element accumulation in fishes collected from coastal waters of the Caspian Sea

Concentrations of 13 trace elements (V, Mn, Cr, Co, Cu, Zn, Se, Mo, Ag, Cd, Hg, Tl and Pb) were determined in muscle of bony fishes collected from coastal areas of the Caspian Sea (Kazakhstan, Azerbaijan, Turkmenistan and Iran). In all the fishes, Zn concentration was highest, followed by Cu, Se, Mn and Co, while levels of toxic elements (Ag, Cd, Cd, Tl and Pb) were relatively low. Concentrations of several elements were significantly varied between the species in each sampling area. For most of the trace elements examined, the concentrations decreased significantly with body weight of fishes. In contrast, a positive correlation with body weight was found for Co, Se and Pb concentrations in one fish species, and Hg in 2 fish species. Geographical difference in the concentrations of trace elements was examined using the Caspian roach collected from five stations of Iranian coastal waters. The concentrations of Co, Mo, Ag, Cd and Tl were higher in fishes from western stations than those from eastern stations, whereas the opposite trend was observed for Hg, indicating that local sources of trace metal pollution may be present in the Iranian coastal areas of the Caspian Sea. Levels of trace elements in Caspian fishes were relatively low in comparison to those of other regions, but Zn and Hg levels in some specimens exceeded the guideline values for food.     

Ultrasound‐Assisted Emulsification–Microextraction Combined with Graphite Furnace Atomic Absorption Spectrometry for the Determination of Trace Lead in Water

The ultrasound‐assisted emulsification–microextraction (USAEME) method was combined with graphite furnace atomic absorption spectrometry (GFAAS) for the determination of trace Pb using dithizone (H²DZ) as chelating reagent. Some effective parameters influenced the detection and microextraction, such as ashing temperature and atomization temperature, pH, extraction solvent, sample volume, extraction time, and extraction temperature were selected and optimized. After extraction, the calibration curves for Pb was in the concentration range of 0.1–10 ng mL^?1, and the linear equation was y = 0.097 x + 0.023 (R = 0.99). Under the optimized conditions, the detection limit of the method was 20 pg mL^?1 with an enrichment factor of 70 and the relative standards deviation (RSD) for seven determinations of 1 ng mL^?1 Pb was 11%. The proposed method was successfully applied to determine trace Pb in Yueya Lake water, pond water, and spiked samples. Furthermore, a certified reference material of Environment Water (GBW08607) was analyzed and the determined value was in good agreement with the certified value, which showed the accuracy, recovery, and applicability of the reported method.     

Groundwater in the wetlands of the Okavango Delta, Botswana, and its contribution to the structure and function of the ecosystem

The Okavango Delta of northern Botswana is a large (40,000 km²) alluvial fan located at the terminus of the Okavango River. The river discharges about 10 km³ of water onto the fan each year, augmented by about 6 km³ of rainfall, which sustains about 2500 km² of permanent wetland and up to 8000 km² of seasonal wetland. Interaction between this surface water and the groundwater strongly influences the structure and function of the wetland ecosystem. The climate is semi-arid, and only 2% of the water leaves as surface flow and probably very little as groundwater flow. The bulk of the water is lost to the atmosphere. The Okavango River also delivers about 170,000 tonnes of bedload sediment and about 360,000 tonnes of solutes to the Delta each year, most of which are deposited on the fan. Bedload is deposited in the proximal, permanent wetland, whilst much of the solute load is deposited in the seasonal wetland. Notwithstanding the high evapotranspirational loss, saline surface water is rare. Between 80 and 90% of the seasonal flood water infiltrates the ground, recharging the groundwater beneath the flood plains and the many islands on the flood plains. The remainder is lost by evaporation. This groundwater reservoir is transpired into the atmosphere by both aquatic vegetation on the flood plains and terrestrial vegetation on the islands, and the water table is steadily lowered following passage of the seasonal flood. Trees, which are almost exclusively confined to islands, are particularly important, as they lower the water table beneath islands relative to the surrounding wetlands. There is therefore a net flow of groundwater towards islands. Accumulation of dissolved salts in this groundwater leads to precipitation of solutes (mainly of silica and calcite) in the soils beneath island fringes and the islands grow by vertical expansion. Islands are thus an expression of the chemical sedimentation taking place on the fan. Sodium bicarbonate accumulates in the groundwater beneath island centres, and this impacts on the vegetation, leading ultimately to barren island interiors. Dense saline brine thus produced subsides under density-driven flow. This cycling of seasonal flood water through the groundwater reservoir thus plays a key role in creating and maintaining the biological and habitat diversity of the wetland, and inhibits the formation of saline surface water.     

Coastal protection of the isle of usedom — conceptional design of an offshore breakwater system at the streckelsberg, Baltic Sea

The Isle of Usedom is located in the South of the Baltic Sea on the border between Poland and Germany. The Streckelsberg is midway along the coastline of the island. The cliff coast area is extremely exposed to waves.Coastal protection works have been carried out here for the last 100 years, starting in 1895 with the construction of a revetment. All efforts could not solve the erosion problems in the long-term. Therefore, it was decided to install a new system of coastal protection measures in 1994. The conceptional design includes a system of three offshore breakwaters in combination with a beach nourishment system. To minimize downdrift erosion a groyne scheme will be additionally installed.The aim of the offshore breakwaters is to reduce the wave energy transformed into the sheltered area and to consequently reduce the longshore sediment transport. It is expected to support the natural development of a salient which will form the main part of the complete coastal protection system.     

Groundwater–surface water interactions in a lowland watershed: source contribution to stream flow

The lower coastal plain of the Southeast USA is undergoing rapid urbanisation as a result of population growth. Land use change has been shown to affect watershed hydrology by altering stream flow and, ultimately, impairing water quality and ecologic health. However, because few long‐term studies have focused on groundwater–surface water interactions in lowland watersheds, it is difficult to establish what the effect of development might be in the coastal plain region. The objective of this study was to use an innovative improvement to end‐member mixing analysis (EMMA) to identify time sequences of hydrologic processes affecting storm flow. Hydrologic and major ion chemical data from groundwater, soil water, precipitation and stream sites were collected over a 2‐year period at a watershed located in USDA Forest Service's Santee Experimental Forest near Charleston, South Carolina, USA. Stream flow was ephemeral and highly dependent on evapotranspiration rates and rainfall amount and intensity. Hydrograph separation for a series of storm events using EMMA allowed us to identify precipitation, riparian groundwater and streambed groundwater as main sources to stream flow, although source contribution varied as a function of antecedent soil moisture condition. Precipitation, as runoff, dominated stream flow during all storm events while riparian and streambed groundwater contributions varied and were mainly dependent on antecedent soil moisture condition. Sensitivity analyses examined the influence of 10% and 50% increases in analyte concentration on EMMA calculations and found that contribution estimates were very sensitive to changes in chemistry. This study has implications on the type of methodology used in traditional forms of EMMA research, particularly in the recognition and use of median end‐member water chemistry in hydrograph separation techniques. Potential effects of urban development on important hydrologic processes (groundwater recharge, interflow, runoff, etc.) that influence stream flow in these lowland watersheds were qualitatively examined. Copyright © 2011 John Wiley & Sons, Ltd.