Phosphorous speciation in surface sediments of the Cochin estuary

Sequential chemical extraction using chelating agents were used to study the P dynamics and its bioavailability along the surface sediments of the Cochin estuary (southwest coast of India). Sediments were analyzed for major P species (iron bound P, calcium bound P, acid soluble organic P, alkali soluble organic P and residual organic P), Fe, Ca, total carbon, organic carbon, total nitrogen and total sulfur contents. An abrupt increase in the concentration of dissolved inorganic P with increasing salinity was observed in the study region. Iron-bound P exhibited a distinct seasonal pattern with maximum values in the monsoon season when fresh water condition was prevailed in the estuary. As salinity increased, the percentage of iron-bound P decreased, while that of calcium-bound P and total sedimentary sulfur increased. C/P and N/P ratios were low which indicate that large amounts of organic matter enriched with P tend to accumulate in surface sediments. The high organic P contribution in the sedimentary P pool may indicate high organic matter load with incomplete mineralization, as well as comparatively greater percentage of humic substance and resistant organic compounds. Principal component analysis is employed to find the possible processes influencing the speciation of P in the study region and indicate the following processes: (1) the spatial and seasonal variations of calcium bound P and acid soluble organic P was mainly controlled by sediment texture and organic carbon content, (2) sediment redox conditions control the distribution of iron bound P and (3) the terrigenous input of organic P is a significant processes controlling total P content in surface sediments. The bioavailable P was very high in the surface sediments which on an average accounts for 59 % in the pre-monsoon, 65 % in the monsoon and 53 % in the post-monsoon seasons. The surface sediments act as a potential internal source of P in the Cochin estuary.     

Trace metal speciation and contamination in an intertidal estuary

An analysis of the geochemical distribution of selected trace metals among various geochemical phases of the sediments in the Tees estuary was carried out using a sequential extraction technique and Differential Stripping Voltammetry. The sediments of the estuary are mainly organic rich clay silts and metal concentrations exceed those in the water column. Speciation results show that contamination of the estuary is mainly from anthropogenic sources. Pb and Zn are associated with the reducible, residual and oxidisable fractions. The speciation pattern of Cd was similar to those of lead and zinc. However there were also some exchangeable and bound to carbonate fractions although these were less significant. Cu is largely associated with the oxidisable and residual fractions, with insignificant bound to carbonate, exchangeable and reducible fractions. The most bioavailable forms of the metals are the free inorganic ions. Total metal concentrations in the estuary display a downward trend since the 1970s.     

Assessment and sources of nonaromatic hydrocarbons in surface sediments of three harbors in Santa Catarina State, Brazil

Nonaromatic hydrocarbons and geochemical parameters from 17 sediment?Cwater interface samples were used to assess sources of organic matter in three harbors, located in Santa Catarina State, southern Brazil. The evaluation was based on the molar C/N/P ratios, abundance of resolved nonaromatic hydrocarbons (3.0?C25.9 ??g g^???1), unresolved complex mixture, and two indexes: the carbon preference index (CPI) and the low molecular weight to high molecular weight ratio. The results indicate that the organic matter is predominantly of terrestrial origin (C/N > 10 and CPI > 2). Variations in the total organic carbon from 0.43 to 2.98 mmol g^???1 and total phosphorus from 82.4 to 464.3 ??g g^???1 showed no clear correlation with the silt and clay fractions of the sediments possibly due to anthropogenic input. In contrast to the low level of contamination based on the acyclic hydrocarbon distribution, the results obtained from a series of geologically stable hopanes and steranes reveal the presence of less degradable petroleum derivatives.     

Optimizing the weight loss-on-ignition methodology to quantify organic and carbonate carbon of sediments from diverse sources

The sequential weight loss-on-ignition (WLOI) method for determination of organic and carbonate or inorganic carbon (C) content was evaluated on sediments from diverse sources with a great range of C contents. The sediments were collected from canal, wetland, river, estuary, lake, and marine sites. The organic and inorganic C contents of these samples ranged from 1 to 430 g kg^???1 and from 4 to 97 g kg^???1, respectively. Combinations of the combustion time and temperature and optimal weight ranges of representative samples were tested, and comparisons of the WLOI method with other methods, including dry combustion and wet combustion, were made. These methods were (1) use of the carbon?Cnitrogen?Csulfur (CNS) autoanalyzer with normal and reduced temperatures for total and organic C, (2) thermogravimetry for both organic and inorganic C, (3) use of the CNS autoanalyzer after removal of inorganic (carbonate) C by fumigating samples with concentrated HCl for organic C, (4) Walkley?CBlack wet combustion method for organic C, and (5) pressure-calcimeter associated with subtraction method (total C minus inorganic C) for organic C determinations. The results of analyzing samples of sediments of diverse origins showed that the optimal combination of temperature and time of WLOI depended mostly on the sources of the analyzed sediment. The WLOI analysis of sediment samples for organic C from wetlands, canal, estuary, or river sites needed a relatively low temperature but that of sediment samples from lake and marine sites required a relatively high temperature. Overall, to obtain reliable analysis results of samples from widely varied sediment sources except marine sediments, 500°C for 12 h was optimal for organic C content determination, and 800°C for yet another 12 h was optimal for inorganic C content determination. The temperature could even be reduced to 475°C if only wetland and stream sediments were included, but for marine sediments, 550°C for 12 h was necessary. Precise C content determinations for most sediment sources could be obtained by WLOI when sample quantities ranged from 2.0 to 4.0 g. The WLOI method, when conducted properly, resulted in precise measurements of C contents in ??standard samples?? used for calibration, and these values were closely comparable to results obtained with other dry combustion methods (R ²????0.96). We conclude that WLOI, which has advantages of simplicity, cost-effectiveness, and no waste disposal over other methods, can provide precise measurements of organic and inorganic C contents in sediments from a wide range of sources, but the selection of heating temperature and exposure time should be carefully considered based on sediment sources.     

Eutrophication induced changes in benthic community structure of a flow-restricted tropical estuary (Cochin backwaters), India

The influence of anthropogenic loading on the distribution of soft bottom benthic organisms of a tropical estuary (Cochin backwaters) was examined. The industrial activities were found to be high in the northern and central part of the estuary, where dissolved inorganic nitrogen (DIN > 210 ??M) and phosphorus (DIP > 6.5 ??M) have caused high abundance of chlorophyll a (up to 73 mg m^???3) and accumulation of organic carbon in sediments (up to 5%). Principal component analysis distinguished three zones in the estuary. The central zone (Z1) was characterized by organic enrichment, low species diversity, and increased number of pollution tolerant species. Long-term deterioration of the estuary is indicated by an increase in the nutrients and chlorophyll a levels by sixfold during the last few decades. Flow restrictions in the lower estuary have lead to a fourfold increase in sediment organic carbon over the period of three decades. The reduced benthic diversity followed by an invasion of opportunistic polychaetes (Capitella capitata), are indicative of a stress in the estuary.     

Levels of polycyclic aromatic hydrocarbons (PAHs) in the Densu River Basin of Ghana

The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) in Densu River Basin in Ghana were measured using gas chromatograph. Surface water samples were collected from nine stations, namely, Potroase, Koforidua Intake, Suhyien, Mangoase, Asuboi, Nsawam Bridge, Afuaman, Ashalaga, and Weija Intake in the Densu Basin. Total PAH concentrations varied from 13.0 to 80.0 ??g/mL in the Densu River, with a mean value of 37.1 ??g/mL. The two- to three-ring PAHs (low-molecular-weight PAHs) were found to be dominant in the Densu River Basin. Total PAH concentrations showed the following pattern: Koforidua Intake (80.0 ??g/mL) > Asuboi (50.8 ??g/mL) > Afuaman (47.9 ??g/mL) > Weija Intake (45.0 ??g/mL) > Suhyien (27.6 ??g/mL) > Nsawam (23.5 ??g/mL) > Ashalaja (22.9 ??g/mL) > Potroase (23.3 ??g/mL) > Mangoase (13.0 ??g/mL). According to the Agency for Toxic Substances and Disease Registry (ATSDR), background levels of PAHs in drinking water supplies in the USA range from 0.004 to 0.024 ??g/mL. PAH levels from all sites exceeded the range set by ATSDR. B[a]P contributed the highest carcinogenic exposure equivalent (0.3 ??g/mL), followed by B[a]A (0.132 ??g/mL) and B[b]F (0.08 ??g/mL), contributing 52.6%, 23.2%, and 4.6%, respectively, of the total carcinogenicity of surface water PAH in the Densu River Basin. The carcinogenic potency was estimated to be 0.57 ??g/mL. The presence of PAHs was an indication of the water sources being contaminated, with potential health implications.     

Associations of cadmium, zinc, and lead in soils from a lead and zinc mining area as studied by single and sequential extractions

An exploratory study of the area surrounding a historical Pb?CZn mining and smelting area in Zawar, India, detected significant contamination of the terrestrial environment by heavy metals. Soils (n?=?87) were analyzed for pH, EC, total organic matter (TOM), Pb, Zn, Mn, and Cd levels. The statistical analysis indicated that the frequency distribution of the analyzed parameters for these soils was not normal. The median concentrations of metals in surface soils were: Pb 420.21 ?? g/g, Zn 870.25 ?? g/g, Mn 696.70 ?? g/g, and Cd 2.09 ?? g/g. Zn concentrations were significantly correlated with Cd (r?=?0.867), indicating that levels of Cd are dependent on Zn. However, pH, electrical conductivity and total organic matter were not correlated significantly with Cd, Pb, Zn, and Mn. To assess the potential mobility of Cd, Pb, and Zn in soils, single (EDTA) as well as sequential extraction scheme (modified BCR) were applied to representative (n?=?23) soil samples. The amount of Cd, Pb, and Zn extracted by EDTA and their total concentrations showed linear positive correlation, which are statistically significant (r values for Cd, Pb, and Zn being 0.901, 0.971, and 0.795, respectively, and P values being <0.001). The correlation coefficients indicate a strong relation between EDTA-extractable metal and total metal. These results appear to justify the use of ??total?? metal contents as a useful preliminary indicator of areas where the risks of metal excess or deficiency are high. The EDTA extractability was maximum for Cd followed by Pb and Zn in soils from all the locations. As indicated by single extraction, the apparent mobility and potential bioavailability of metals in soils followed the order: Cd ?? Pb >?> Zn. Soil samples were sequentially extracted (modified BCR) so that solid pools of Cd, Zn, and Pb could be partitioned into four operationally defined fractions viz. acid-soluble, reducible, oxidizable, and residual. Cadmium was present appreciably (39.41%) in the acid-soluble fraction and zinc was predominantly associated (32.42%) with residual fraction. Pb (66.86%) and Zn (30.44%) were present mainly in the reducible fraction. Assuming that the mobility and bioavailability are related to solubility of geochemical forms of metals and decrease in the order of extraction, the apparent mobility and potential metal bioavailability for these contaminated soil samples is Cd > Zn > Pb.     

Flame ionization gas chromatographic determination of phthalate esters in water, surface sediments and fish species in the Ogun river catchments, Ketu, Lagos, Nigeria

The detection and quantification of four phthalate esters??dimethyl phthalate (DMP), diethyl phthalate (DEP), dibutyl phthalate (DBP), and diethylhexyl phthalate (DEHP)??in water, sediment, and some fish species were carried out using flame ionization gas chromatography. The samples were collected from the Ogun river catchments, Ketu, Lagos. The DMP was not detected in the water and fish samples but was detected in sediments collected from four of the six sampling sites. The concentration of DEP, DBP, and DEHP in the fish species ranged from 320.0?C810.0, 380.0?C1,080.0, and 40.0?C150.0 ??g/kg in Tilapia sp.; 310.0?C860.0, 400.0?C1,170.0, and 40.0?C110.0 ??g/kg in Chrysichthys sp.; and 320.0?C810.0, 400.0?C3,970.0, and 30.0?C300.0 ??g/kg (DEHP) in Synodontis sp., respectively. The differences in fish phthalate levels are not statistically significant at p?<?0.05, an indication that phthalate esters accumulation is not fish species dependent. The DEP, DBP, and DEHP values recorded are considerably higher than the maximum allowed concentrations for drinking water prescribed by the US Environmental Protection Agency. The phthalate pollution index and biosediment accumulation factor values were also calculated.     

Evaluation of environmental impacts of Integrated Industrial Estate��Pantnagar through application of air and water quality indices

Large-scale industrialization, population inflow, and rapid urbanization coupled with unfavorable meteorological conditions often induce significant degradation of urban environment. In order to assess the extent of environmental impacts due to establishment of the Integrated Industrial Estate??Pantnagar (IIE-Pantnagar), ambient air and groundwater were monitored from June 2007 to May 2008. Collected baseline information was normalized and interpreted with the application of air (AQI) and water quality indices (WQI). Among the pre-identified air pollutants, suspended particulate matter was found to be the principal culprit to deteriorate ambient air quality, with a maximum annual concentration of 418.5 ??g/m³. Monthly average concentrations of respirable particulate matter (aerodynamic diameter < 10 ??m) also persist at a critical level with an annual maximum of 207.3 ??g/m³. A segmented linear function with maximum operator concept was used to compute AQI, and the developed index was found well suitable to demonstrate temporal variations of ambient air quality. The computed AQI value for the selected study region varied from moderate (97.0) to very poor pollution level (309.2) in respect to developed air quality standards. Furthermore, an integrated WQI was developed comprising 9 parameters, and among all the 10 pre-identified locations, the average groundwater quality was found acceptable in terms of Indian drinking water standards. The maximum WQI (70.6) was found at the Kichha Railway Station during summer months, revealing moderate pollution load. Industrial discharge from IIE-Pantnagar coupled with other industrial setup may hold responsible for such kind of degradation of water quality. In contrast, WQI computed at Rudrapur City demonstrate minimum (15.0?C22.1) pollution load. For 95% of the monitoring period, the computed WQI was found acceptable for all selected locations with few exceptions. The application of WQI to assess temporal variations in groundwater quality was therefore found satisfactory.     

Phosphorus speciation in the marine sediment of Kalpakkam coast,southeast coast of India

A study was carried out at Kalpakkam coast to find out the distribution of various fractions of phosphorus (P) in the marine sediment during pre-northeast monsoon period. Samples were collected from ten locations covering ~80 km² of the inner-shelf region. Sedimentary parameters such as sand, silt, clay, and organic carbon percentage were analyzed in order to find out their relation with various P fractions. The sediment was found to be predominantly sandy in nature with low silt and clay content. Among all the fractions (loosely bound (LoP), calcium bound (CaP), iron bound (FeP), aluminum bound (AlP), and organic (OP)), CaP fraction constituted the largest portion (68.7 %) followed by organic fraction (16.3 %). The bioavailable P fractions ranged from 5 to 44 % of the total P (TP) content. Relatively high LoP content was observed at the offshore locations with comparatively high mud percentage as compared with the near-shore locations. As FeP and AlP concentrations were directly proportional to the amount of fine-grain sediment, the low levels of these fractions found in this coastal area were therefore attributed to the sandy nature of the sediments. The order of abundance of the major forms of P in the surface sediments of Kalpakkam coast was as follows: CaP?>?OP?>?LoP?>?AlP?>?FeP.     

Investigation into presence of atmospheric particulate matter in Marikana, mining area in Rustenburg Town, South Africa

An investigation to find out presence of particulate matter in Marikana, a mining area in Rustenburg town, South Africa, was carried out in the months of August and November of 2008. Samples were collected for measurements of particulate matter (PM) of particle diameters of PM10, PM2.5, and PM1. After gravimetric analysis of daily measurements, it was found that PM10 concentration values ranged between 3 and 9 ??g/m³, PM2.5 concentration values ranged between 16 and 26 ??g/m³, and PM1 concentration values ranged between 14 and 18 ??g/m³ for the month of August 2008. For the month of November, it was found that PM10 concentration values ranged between 2 and 8 ??g/m³, PM2.5 concentration values ranged between 0 and 5 ??g/m³, and PM1 concentration values ranged between 4 and 15 ??g/m³. This study was undertaken as preliminary work having in mind that mining activities could be emitting high levels of particulate matter in the atmosphere which might be degrading the quality of the air. It was observed, however, that the daily particulate matter especially of PM10 emitted were quite low when compared to laid down International Air Quality Standards. The standards did not give guidelines for particulate matter of diameter 2.5 ??m. It was concluded that particulate matter came from three major sources: platinum mining, domestic biomass burning, and traffic emissions due to fuel burning.     

Investigation and assessment of volatile organic compounds in water sources in China

456 water samples collected from 152 water sources in 2006 were analyzed for 21 volatile organic compounds (VOCs). Concentrations of 21 VOCs ranged from below method detection limits of the laboratory to 7.65 ??g/L (toluene), but seldom exceeded the concentration limits set in the National Drinking Water Quality Standards (GB5749-2006) or the National Environmental Quality Standards for Surface Water (GB3838-2002) of China. Of the 21 individual VOCs analyzed, 11 VOCs were detected in at least one sample at or above 1.0 ??g/L; 6.6% of the water samples had a detection of at least one VOC at or above 1.0 ??g/L, and 2.6% had a detection of at least two VOCs at or above 1.0 ??g/L. Based on the statistical data of detection frequencies above the method detection limits, 75% of the samples detected at least one VOC, and 65% of the samples detected at least two VOCs. Chloroform, toluene, and 1,2-dichloroethene were the three most frequently detected VOCs, with detection frequencies of 76.97%, 68.42%, and 44.08%, respectively. Volatile halogenated hydrocarbons and gasoline components were the two most frequently detected VOC groups.     

Assessment of the labile fractions of copper and zinc in marinas and port areas in Southern Brazil

The dissolved labile and labile particulate fractions (LPF) of Cu and Zn were analyzed during different seasons and salinity conditions in estuarine waters of marina, port, and shipyard areas in the southern region of the Patos Lagoon (RS, Brazil). The dissolved labile concentration was determined using the diffusive gradients in thin films technique (DGT). DGT devices were deployed in seven locations of the estuary for 72 h and the physicochemical parameters were also measured. The LPF of Cu and Zn was determined by daily filtering of water samples. Seasonal variation of DGT–Cu concentrations was only significant (p?<?0.05) at one shipyard area, while DGT–Zn was significant (p?<?0.05) in every locations. The LPF of Cu and Zn concentrations demonstrated seasonal and spatial variability in all locations, mainly at shipyard areas during high salinity conditions. In general, except the control location, the sampling locations showed mean variations of 0.11–0.45 μg?L^?1 for DGT–Cu, 0.89–9.96 μg?L^?1 for DGT–Zn, 0.65–3.69 μg?g^?1 for LPF–Cu, and 1.35–10.87 μg?g^?1 for LPF–Zn. Shipyard areas demonstrated the most expressive values of labile Cu and Zn in both fractions. Strong relationship between DGT–Zn and LPF–Zn was found suggesting that the DGT–Zn fraction originates from the suspended particulate matter. Water salinity and suspended particulate matter content indicated their importance for the control of the labile concentrations of Cu and Zn in the water column. These parameters must be taken into consideration for comparison among labile metals in estuaries.     

Coelomocyte biomarkers in the earthworm Eisenia fetida exposed to 2,4,6-trinitrotoluene (TNT)

Contamination by 2,4,6-trinitrotoluene (TNT) is a global environmental problem at sites of former explosive production, handling, or storage, and could have deleterious consequences for human and ecological health. We investigated its sublethal effects to Eisenia fetida, using two nonspecific biomarkers. In coelomocytes of earthworms exposed 24, 48, or 72 h, we evaluated DNA damage (comet assay) and neutral red retention time (NRRT), using the filter paper contact test. Both percentage of damage (D%) and calculated damage index showed significant DNA damage at almost all concentrations, at all time points assayed. Along exposure time, two different patterns were observed. At the lower TNT concentrations (0.25?C0.5 ??g/cm²) an increased DNA migration at 48 h, with a decrease close to initial levels after 72 h exposure, was observed. This decrease could be attributed to activation of the DNA repair system. At higher concentrations (1.0?C2.0 ??g/cm²), the high DNA damage observed remained constant during the 72 h exposure, suggesting that the rate of DNA repair was not enough to compensate such damage. Analysis of NRRT results showed a significant interaction between time and treatment. After 48 h, a significant decrease was observed at 4.0 ??g/cm². After 72 h, NRRT presented a concentration-dependent decrease, significantly different with respect to control at 0.5, 1.0, 2.0, and 4.0 ??g/cm². The two assayed methods, performed on the same sample, showed clear responses to sublethal TNT exposure in E. fetida, providing sensitive unspecific biomarkers of cell injury and DNA damage.     

Variation and removal efficiency of assimilable organic carbon (AOC) in an advanced water treatment system

This study investigates the microorganism growth indicator and determines the assimilable organic carbon (AOC) content at the Cheng-Ching Lake Advanced Water Treatment Plant (CCLAWTP) in Kaohsiung, Taiwan. Notably, AOC is associated with the biological stability within the water distribution network and has garnered considerable attention in the environmental engineering field in recent years. Water samples were collected from the effluent of each unit in CCLAWTP once monthly during December 2008 to November 2009. Items of water quality related to carbon concentration levels, including AOC, total organic carbon, dissolved organic carbon, UV₂₅₄, and specific ultraviolent absorbance were analyzed. Analytical results demonstrate that the average AOC concentration in raw water was 83.61 ??g/L and reduced in freshwater was controlled at an average of 50 ??g/L after an advanced treatment system of roughly 54% of AOC was removed in compliance with treatment plant standards. If AOC concentrations in freshwater can be reduced, study results can provide a direction for improving water treatment capabilities.     

Environmental vanadium distribution, mobility and bioaccumulation in different land-use Districts in Panzhihua Region, SW China

In order to characterize environmental vanadium distribution, mobility, and bioaccumulation, a total of 55 soil samples and 36 plant samples were collected in four typical land-use districts in Panzhihua region, Southwestern China. Soil samples were analyzed with the modified Community Bureau of Reference (BCR) sequential extraction procedure, and the content of vanadium in soil and plant was determined by ICP-AES. The total content of vanadium was 208.1?C938.4 mg kg^???1 in smelting area, 111.6?C591.2 mg kg^???1 in mining area, 94.0?C183.6 mg kg^???1 in urban park, and 71.7?C227.2 mg kg^???1 in agricultural area, respectively, while the bio-available content of vanadium was characterized that the polluted areas (mining area 18.8?C83.6 mg kg^???1, smelting area 41.7?C132.1 mg kg^???1) and the unpolluted area (agricultural area 9.8?C26.4 mg kg^???1, urban park 9.9?C25.2 mg kg^???1). In addition, the contamination degree of vanadium in soil was smelting area > mining area > agricultural area ?? urban park. Moreover, the fraction of vanadium in each sequential extraction characterized that residual fraction > oxidizable fraction > reducible fraction > acid soluble fraction. The bioaccumulation of vanadium from soil to plant was weak to intermediate absorption. Therefore, some countermeasures such as soil monitoring and remediation should be to take in the sooner future, especially in mining and smelting area.     

Personal, indoor, and outdoor exposure to VOCs in the immediate vicinity of a local airport

This study measures the effect of emissions from an airport on the air quality of surrounding neighborhoods. The ambient concentrations of benzene, toluene, ethylbenzene, and o-, m-, and p-xylene (BTEX) were measured using passive samplers at 15 households located close to the airport (indoor, outdoor, and personal), at the end of airport runways and an out-of-neighborhood location. Measurements occurred over a 48-h period during summer 2006 and winter 2006?C2007. The average concentrations were 0.84, 3.21, 0.30, 0.99, and 0.34 ??g/m³ at the airport runways and 0.84, 3.76, 0.39, 1.22, and 0.39 ??g/m³ in the neighborhood for benzene, toluene, ethylbenzene, m-, p-, and o-xylene. The average neighborhood concentrations were not significantly different to those measured at the airport runways and were higher than the out-of-neighborhood location (0.48, 1.09, 0.15, 0.78, and 0.43 ??g/m³, each BTEX). B/T ratios were used as a tracer for emission sources and the average B/T ratio at the airport and outdoors were 0.20 and 0.23 for the summer and 0.40 and 0.42 for the winter, suggesting that both areas are affected by the same emission source. Personal exposure was closely related to levels in the indoor environment where subjects spent most of their time. Indoor/outdoor (I/O) ratios for BTEX ranged from 1.13 to 2.60 and 1.41 to 3.02 for summer and winter. The seasonal differences in I/O ratios reflected residential ventilation patterns, resulting in increased indoor concentrations of volatile organic compounds during winter.     

Organochlorine pesticides in the surface water and sediments from the Peacock River Drainage Basin in Xinjiang, China: a study of an arid zone in Central Asia

Fourteen surface water and nine surface sediment samples were collected from the Peacock River and analyzed for organochlorine pesticides (OCPs) by gas chromatograph?Celectron capture detector (GC-ECD). All the analyzed organochlorine pesticides, except o,p ^??-DDT, were detected in sediments from the Peacock River; but in the water samples, only ??-HCH, HCB, p,p ^??-DDD, and p,p ^??-DDT were detected at some sites. The ranges for total OCPs in the water and sediments were from N.D. to 195 ng l^???1 and from 1.36 to 24.60 ng g^???1, respectively. The only existing HCH isomer in the water, ??-HCH, suggested that the contamination by HCHs could be attributed to erosion of the weathered agricultural soils containing HCHs compounds. Composition analyses showed that no technical HCH, technical DDT, technical chlordanes, endosulfans, and HCB had been recently used in this region. However, there was new input of ??-HCH (lindane) into the Peacock River. The most probable source was water flowing from Bosten Lake and/or agricultural tailing water that was returned directly into the Peacock River. DDT compounds in the sediments may be derived mainly from DDT-treated aged and weathered agricultural soils, the degradation condition was aerobic and the main product was DDE. HCB in the sediment might be due to the input from Bosten Lake and the lake may act as an atmospheric deposition zone. There was no significant correlation between the concentrations of OCPs (including ??HCH, ??DDT, chlordanes, endosulfans, HCB and total OCPs) and the content of fine particles (<63 ??m). The concentrations of OCPs were affected by salinity.     

Heavy metal contamination in tailings and rocksamples from an abandoned goldminein southwestern Nigeria

Active and abandoned primary and secondary goldmines have been observed to be major sources of metals into the environment. This study assessed the level of metal concentrations in rock and tailing samples collected from the abandoned primary goldmine site at Iperindo. A total of five rock and ten tailing samples were collected for this study. The tailing samples were subjected to physicochemical analysis using standard methods. The samples were analyzed for metals using inductively coupled plasma/optical emission spectrometry technique. The results obtained indicated that tailings were acidic (pH 5.02), with electrical conductivity 133.4 μS/cm, cation exchange capacity 8.95 meq/100 g, available phosphorus was 4.74 mg/L, organic carbon 5.58 %, and organic matter 9.63 %. The trends for metal concentrations within the samples were in the order: Zn?>?Cu?>?Co?>?Pb?>?Cr?>?As?>?Cd for rock samples, Cu?>?Zn?>?Cr?>?Pb?>?As?>?Co?>?Cd in tailing samples. Cd, Pb, and Zn in the rock were above the Abundance of Elements in Average Crustal Rocks standards. Principal component analysis showed higher variations among samples in Iperindo. Cd, Pb, Cr, Co, Cu, As, and Zn were strongly loaded to principal component 1, with these metals significantly contributing to variations in 65.76 % of rock and 53.24 % of tailing. This study suggests that the metal concentration in tailings is a reflection of the metal composition of the rocks.     

Assessment of land influence on a high-latitude marine coastal system: Tierra del Fuego, southernmost Argentina

The study deals with the determination of physico-chemical parameters, inorganic nutrients, particulate organic matter, and photosynthetic pigments on a monthly basis during an annual cycle from nine sampling sites of the coastal zone of a high-latitude ecosystem (Tierra del Fuego, Argentina). Nitrites and phosphates concentrations were similar to other systems of the south Atlantic coast (median, 0.30 and 1.02 ??M, respectively), while nitrates were higher in all sampling periods (median, 45.37 ??M), and silicates were significantly smaller (median, 7.76 ??M). Chlorophyll a and phaeopigments have shown median values of 0.38 and 0.85 mg m^???3, respectively, while saturated values of dissolved oxygen were recorded throughout the study. The analysis reflected that nutrient enrichment seems to be linked to an anthropogenic source, the presence of peatlands areas, and a sink of Nothofagus pumilio woods. The area could be characterized in three zones related to (1) high urban influence, (2) natural inputs of freshwater, and (3) mixed inputs coming from moderate urban impacts.