Anthropogenic nexus on organochlorine pesticide pollution: a case study with Tamiraparani river basin,South India

The levels of 17 organochlorine pesticides residues (OCPs) in surface water and sediments from Tamiraparani river basin, South India were investigated to evaluate their potential pollution and risk impacts. A total of 96 surface water and sediment samples at 12 sampling stations were collected along the river in four seasons during 2008–2009. The ΣOCP concentrations in surface water and sediments were in the range of 0.1 to 79.9 ng l⁻¹ and 0.12 to 3,938.7 ng g⁻¹ dry weight (dw), respectively. Among the OCPs, the levels of dichlorodiphenyltrichloroethanes (DDTs), aldrin, dieldrin, cis-chlordane, trans-chlordane, and mirex were dominant in the sediments. The dominant OCPs in water samples are heptachlor, o,p′-DDE, dieldrin, o,p′-DDD, and mirex, which show different source of contamination pattern among sampling seasons. The distribution pattern of DDTs, hexachlorocyclohexane, and other OCPs in the present study shows heterogenic nature of nonpoint source of pollution. Notable contamination of water and sediment sample that was observed in upstream (S2) 58 ng l⁻¹ and downstream (S11) 1,693 ng g⁻¹ dw explains agricultural and municipal outfalls, whereas frequent damming effect reduces the concentration level in the midstream. The overall spatial–temporal distribution pattern of ΣOCP residues are illustrated by GIS package.     

Phosphorus fractions and adsorption characteristics of floodplain sediments in the lower reaches of the Hanjiang River, China

The phosphorus fractions and adsorption characteristics of seven floodplain sediment samples collected in the lower reaches of China’s Hanjiang River were studied. Most phosphorus fractions showed a marked downstream increase in response to point-source inputs from urban areas. Total phosphorus (TP) contents in the sediments ranged from 603.68 to 945.25 mg.kg⁻¹. Inorganic phosphorus (IP) was the major component of TP, and calcium-bound phosphorus (Ca–P) was the major fraction of IP. The distribution characteristics of the phosphorus contents were affected by sediment grain size and hydrodynamic conditions. The maximum phosphorus adsorption capacities (Q _max) and the half-saturation concentration (k) were obtained using an improved Langmuir model. Native adsorbed exchangeable phosphorus content (w _NAP) and the zero-equilibrium phosphorus concentration value (c _EPC0) were subsequently calculated. The effects of sediment grain size, temperature, and disturbance on the phosphorus adsorption isotherms were also studied. The results showed that phosphorus adsorption on floodplain sediments was primarily chemisorption; the particle concentration effect played a more important role at a disturbance intensity of 150 r.min⁻¹ (on a shaker table) than at 100 r.min⁻¹.     

Heavy metals in water, sediment and tissues of Liza saliens from Esmoriz–Paramos lagoon, Portugal

Esmoriz–Paramos lagoon is an ecosystem of great ecological importance that is located on the northwest coast of Portugal and has been degraded as a result of industrial and anthropogenic activities. Concentrations of heavy metals (Cr, Cu, Pb and Zn) were measured in water, sediment and in tissues (liver and muscle) of Liza saliens, which is the dominant fish from the lagoon. Comparisons between metal concentrations in water and sediments were made with those in tissues of fish caught at the lagoon. Metals in water were quantified predominantly bound to particulate and equalled or exceeded the limit of chronic reference values. Metal concentrations in sediments varied among sampled sites. The relative order of concentrations was “Zn > Cu ∼ Pb > Cr” the same pattern observed for metals in water. Metals in fish tissues showed higher concentrations in liver (262 mg Cu·Kg⁻¹ and 89 mg Zn·Kg⁻¹) than in muscle (<3 mg Cu·Kg⁻¹ and 26 mg Zn·Kg⁻¹), while Pb and Cr were not detected. These results suggest that Cu and Zn are the metals of major concern in the lagoon. Mullet detritivorous feeding habits, bioaccumulation pattern and the high sediment metals concentrations relative to the water suggest that sediments can be the most important source of contamination in this ecosystem. The positive relationship found between Cu in liver and fish length demonstrates that time of exposure is a crucial factor in bioaccumulation. Condition indices (K and HSI) in mullets from the lagoon were higher compared to mullets from sea, suggesting abnormal condition in the lagoon population. We conclude that metals chronic exposure in the lagoon can impose considerable fish stress. The results also show that the lagoon is an area of environmental concern.     

Quantifying Carbon Budgets Of Conifer Mediterranean Forest Ecosystems, Turkey

Abstact Aboveground biomass, aboveground litterfall, and leaf litter decomposition of five indigenous tree stands (pure stands ofPinus brutia,Pinus nigra,Cedrus libani,Juniperus excelsa, and a mixed stand ofAbies cilicica,P. nigra, andC. libani) were measured in an eastern Mediterranean evergreen needleleaf forest of Turkey. Measurements were converted to regional scale estimates of carbon (C) stocks and fluxes of forest ecosystems, based on general non-site-specific allometric relationships. Mean C stock of the conifer forests was estimated as 97.8± 79 Mg C ha⁻¹consisting of 83.0 ± 67 Mg C ha⁻¹in the aboveground and 14.8 ± 12 Mg C ha⁻¹in the belowground biomass. The forest stands had mean soil organic carbon (SOC) and nitrogen (SON) stocks of 172.0 ± 25.7 Mg C ha⁻¹and 9.2 ± 1.2 Mg N ha⁻¹, respectively. Mean total monthly litterfall was 376.2± 191.3 kg C ha⁻¹, ranging from 641 ± 385 kg C ha⁻¹forPinus brutiato 286 ± 82 kg C ha⁻¹forCedrus libani. Decomposition rate constants (k) for pine needles were 0.0016 forCedrus libani, 0.0009 forPinus nigra, 0.0006 for the mixed stand, and 0.0005 day⁻¹forPinus brutiaand Juniperus excelsa. Estimation of components of the C budgets revealed that the forest ecosystems were net C sinks, with a mean sequestration rate of 2.0 ± 1.1 Mg C ha⁻¹ yr⁻¹ranging from 3.2 ± 2 Mg C ha⁻¹forPinus brutiato 1.6 ± 0.6 Mg C ha⁻¹forCedrus libani. Mean net ecosystem productivity (NEP) resulted in sequestration of 98.4 ± 54.1 Gg CO₂ yr⁻¹from the atmosphere when extrapolated for the entire study area of 134.2 km²(Gg = 10⁹ g). The quantitative C data from the study revealed the significance of the conifer Mediterranean forests as C sinks     

Facile and Sensitive Spectrophotometric Determination of Carbosulfan in Formulations and Environmental Samples

Facile, selective and sensitive spectrophotometric method has been developed for the determination of carbosulfan in insecticidal formulations, fortified water, food grains, agriculture wastewater and soil samples with newly synthesized reagents. The method was based on acid and alkaline hydrolysis of the carbosulfan pesticide, and the resultant hydrolysis product of carbosulfan was coupled with 2,6-dibromo-4-methylaniline to give a yellow color product with λ _max of 464 nm or interaction with 2,6-dibromo-4-nitroaniline to produce yellow colored product with λ _max of 408 nm or coupling with 2,4,6-tribromoaniline to form red colored product has a λ _max of 471 nm. Under optimal conditions, Beer’s law range for 2,6-dibromo-4-methylaniline (DBMA) was found to be 0.2–12.0 μg ml⁻¹, 0.6–16.0 μg ml⁻¹ for 2,6-dibromo-4-nitroaniline (DBNA) and 0.4–15.0 μg ml⁻¹ for 2,4,6-tribromoaniline (TBA). The molar absorptivity of the color systems were found to be 3.112 × 10⁴ l mol⁻¹ cm⁻¹ for DBMA, 3.214 × 10⁴ l mol⁻¹ cm⁻¹ for DBNA and 3.881 × 10⁴ l mol⁻¹ cm⁻¹ for TBA. Sandell’s of the color reactions are 0.013 μg cm⁻² (DBMA), 0.012 μg cm⁻² (DBNA) and 0.011 μg cm⁻² (TBA) respectively. The effect of the non-target species on the determination of carbosulfan was studied to enhance the selectivity of the proposed methods. The formation of colored derivatives with the coupling agents is instantaneous and stable for 28, 30, and 26 h. Performance of the proposed methods were compared statistically in terms Student’s F and t-tests with the reported methods. An erratum to this article can be found at     

Concentrations of cadmium and lead heavy metals in Dardanelles seawater

Cadmium and lead were determined simultaneously in seawater by differential pulse stripping voltammetry (DPSV) preceded by adsoptive collection of complexes with 8-hydroxyquinoline (oxine) on to a hanging mercury drop electrode (HMDE). In preliminary experiments the optimal analytical condition for oxine concentration was found to be 2.10⁻⁵ M, at pH 7.7, the accumulation potential was −1.1 V, and the initial scannig potential was −0.8 V. The peak potentials were found −0.652 V for Cd and −0.463 V for Pb At the 60 s accumalation time. The limit of detection (LOD) and limit of quantitatification (LOQ) were found to be by voltammetry as 0.588 and 1.959 μg l⁻¹ (RSD, 5.50%) for Cd and 0.931 and 3.104 μg l⁻¹ (RSD, 4.10%) for Pb at 60 s stirred accumulation time respectively. In these conditions the most of the seawater samples are amenable for direct voltammetric determination of cadmium and lead using a HMDE. An adsorptive stripping mechanism of the electrode reaction was proposed. For the comparison, seawater samples were also analysed by ICP-atomic emission spectrometry method (ICP-AES). The applied voltammetric technique was validated and good recoveries were obtained.     

The Distribution and Sources of Polycyclic Aromatic Hydrocarbons in Surface Sediments Along the Egyptian Mediterranean Coast

Coastal marine sediment samples were collected from 31 sampling stations along the Egyptian Mediterranean Sea coast. All sediment samples were analyzed to determine aliphatic and polycyclic aromatic hydrocarbons (PAHs) as well as total organic carbon (TOC) contents and grain size analysis. Total concentrations of 16 EPA-PAHs in the sediments were varied from 88 to 6338 ng g⁻¹ with an average value of 154 ng g⁻¹ (dry weight). However, the concentrations of total aliphatic were varied from 1.3 to 69.9 ng g⁻¹ with an average value of 15.6 ng g⁻¹ (dry weight). The highest contents of PAHs were found in the Eastern harbor (6338 ng g⁻¹), Manzala (5206 ng g⁻¹) and El-Jamil East (4895 ng g⁻¹) locations. Good correlations observed between a certain numbers of PAH concentrations allowed to identify its origin. The average total organic carbon (TOC) percent was varied from 0.91 to 4.54%. Higher concentration of total pyrolytic hydrocarbons (∑COMB) than total fossil hydrocarbons (∑PHE) declared that atmospheric fall-out is the significant source of PAHs to marine sediments of the Egyptian Mediterranean coast. The selected marked compounds, a principal component analysis (PCA) and special PAHs compound ratios (phenanthrene/anthracene vs fluoranthene/pyrene; ∑COMB/∑EPA-PAHs) suggest the pyrogenic origins, especially traffic exhausts, are the dominant sources of PAHs in most locations. Interferences of rather petrogenic and pyrolytic PAH contaminations were noticed in the harbors due to petroleum products deliveries and fuel combustion emissions from the ships staying alongside the quays.     

Sources and distribution of trace metals in the saricay stream basin of southwestern turkey

Seasonal variation of the concentrations of trace metals (Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn) were measured by ICP-AES in the water and sediment from the Saricay Stream, Geyik Dam and Ortakoy Well in the same basin. Comparisons between trace metal concentrations in water and sediment in three sources (Stream, Dam and Well) were made. The concentrations of a large number of trace metals in the water and sediment were generally higher in the Stream than in the Well and Dam, particularly in summer. Trace metal concentration ranges in sediments of the Saricay Stream and its sources showed very wide ranges (as mass ratio): Co: 5–476 μg g⁻¹, Cr: 15–1308 μg g⁻¹, Cu: 7–128 μg g⁻¹, Fe: 1120–13210 μg g⁻¹, Mn: 150–2613 μg g⁻¹, Ni: 102–390 μg g⁻¹, Pb: 0.7–31.3 μg g⁻¹ and Zn: 18–304 μg g⁻¹, whereas Cd was not detected. Trace metal concentration ranges found in waters were: Co: 9.5–20.7 μg L⁻¹, Cr: 20.3–284 μg L⁻¹, Cu: 170–840 μg L⁻¹, Fe: 176–1830 μg L⁻¹, Mn: 29.3–387 μg L⁻¹, and Ni: 4.3–21.9 μg L⁻¹. Among the trace metals studied, Cd and Zn in two seasons and Pb in winter were usually not detected or in the recommended levels. In addition, Cd was not detected in the sediment during the winter season. The analysis of variance (one-way ANOVA) and correlation matrix was employed for the sediment and water samples of the two field surveys (summer and winter) comparison. The three sources showed differences in metal contents. The metal levels in sediments displayed marked seasonal and regional variations, which were attributed to anthropogenic influences and natural processes. In the Saricay Stream, high values of metals during the dry season showed an anthropological effect from small industry firms, e.g.: an olive mill and a dairy farm or water dilution during summer seasons. Finally, the pollution in this basin probably originated from small industrial, low quality coal-burned thermal power plants, and particularly agricultural and domestic waste discharges.     

Spatial and Seasonal Variations in Chlorophyll-Nutrient Relationships in The Shallow Hypertrophic Lake Manyas, Turkey

Regression and correlation analyses were used to predict responses of phytoplankton biomass (chlorophyll) (μg L⁻¹) to nitrate (NO₃) (mg L⁻¹), phosphate (PO₄) (mg L⁻¹) and ammonium (NH₄) (mg L⁻¹) dynamics in the shallow hypertrophic Lake Manyas, Turkey. Nutrient concentrations showed a descending gradient with distance, while chlorophyll concentrations showed an ascending gradient with the distance from the Sığırcı Inlet to the Karadere Outlet. Higher nutrient concentrations did always not coincide with higher chlorophyll concentrations. The results showed that regression models developed using seasonal data were more accurate in predicting chlorophyll concentrations than those developed using the pooled data from whole year (based on R ² and the difference between the measured and predicted values). The findings also revealed that within a single large shallow lake, chlorophyll-nutrient relationships might show significant variations spatially. The objective of this study was to determine the seasonal and spatial variations in the relationships between chlorophyll, nitrate, phosphate and ammonium in the shallow hypertrophic Lake Manyas, Turkey.     

Development of simple and sensitive spectrophotometric method for the determination of bendiocarb in its formulations and environmental samples

Facile, selective and sensitive spectrophotometric method has been developed for the determination of bendiocarb in its insecticidal formulations, fortified water, food grains, agriculture wastewater and agriculture soil samples with prepared reagents. The method was based on alkaline hydrolysis of the bendiocarb pesticide, and the resultant hydrolysis product of bendiocarb was coupled with 2,6-dibromo-4-methylaniline to give a yellow color product with λmaxof457 nmorcouplingwith2, 6−dibromo−4−nitroanilinetoproducearedcoloredproductwithλ_max of474~nmorcouplingwith2, 4, 6−tribromoanilinetoformorangeredcoloredproducthasaλ_max of465 nm.Underoptimalconditions, Beer'slawrangefor2, 6−dibromo−4−methylaniline(DBMA)wasfoundtobe0.6−−14.0~μgmL ^-1, 0.8−−10.0 μgmL ^-1 for2, 6−dibromo−4−nitroaniline(DBNA)and0.4−−10.0 μgmL ^-1 for2, 4, 6−tribromoaniline(TBA).Themolarabsorptivityofthecolorsystemswerefoundtobe4.126~×~10⁴ lmol ^-1 cm ^-1 forDBMA, 3.254×10⁴ l~mol ^-1 cm ^-1 forDBNAand2.812×10⁴ lmol ^-1 cm ^-1 forTBA.Sandell'softhecolorreactionsare0.018 μgcm ^-2(DBMA), 0.052 μgcm ^-2(DBNA)and0.065 μgcm ^-2$ (TBA) respectively. The effect of the non-target species on the determination of bendiocarb was studied. The formation of colored derivatives with the coupling agents is instantaneous and stable for 18 h, 30 h, and 12 h. Performance of the proposed methods were compared statistically in terms Student's F and t-tests with the reported methods.     

Heavy Metal and Trace Elements in Various Fish Samples from Sır Dam Lake, Kahramanmaraş, Turkey

Achanthobrama marmid (thorn-bream) (n:24), Chondrostoma regium (nose-carp) (n:33) and Silurus glanis (wels) (n:21), and Cyprinus carpio (carp) (n:30) were collected from Sır Dam Lake in Kahramanmaraş Province. The iron (Fe), manganese (Mn), cobalt (Co), nickel (Ni), and lead (Pb) levels were determined in the total of 108 fish samples by Atomic Absorption Spectrophotometer. The concentrations of heavy metals were expressed as mg kg⁻¹ wet weight of tissue. The mean Fe and Mn levels of muscle and gill of C. carpio were 0.8–5.71 and 0.30–1.96, respectively. The mean of the Fe and Mn levels of muscle and gill of A. marmid were 1.22, 5.07 and 0.38, 0.85 mg kg⁻¹, respectively. The ranges of mean concentrations of Fe and Mn levels in muscle and gill of C. regium were 0.91, 5.61 and 0.27, 3.42 mg kg⁻¹, respectively. The mean value of Fe in S. glanis gill was 1.03, which of Mn was 0.17 mg kg⁻¹. Fe, Mn, Co, Ni, and Pb were not detected in the muscle of S. glanis. The mean values for Co in muscle of thorn-bream, carp, and nose-carp were 0.005, 0.01, 0.0 mg kg⁻¹, respectively. Nickel values in the muscle were ranged between 0.38 and 1.93 in thorn-bream, 0.06 and 1.34 in carp, 0.14 and 1.89 in nose-carp, in that order. The mean Pb levels of muscle and gill of A. marmid were 0.14 and 0.29 mg kg⁻¹, respectively. The mean values of Pb concentration of muscle and gill for C. carpio were 0.13 and 0.50 mg kg⁻¹, respectively. In C. regium mean values for Pb in muscle and gill were 0.06 and 0.06 mg kg⁻¹, respectively. The mean value of Pb in S. glanis gill was 0.42, ranged between 0.0–0.92 mg kg⁻¹.     

Spatio-Temporal Fluxes in Particulate Organic Carbon in a Tropical Coastal Lagoon

Temporal and spatial variations in particulate organic carbon (POC) in relation to primary production, chlorophyll a, phaeophytin, plankton abundance, secondary production and suspended particulate matter (SPM) were studied monthly for 1 year from April 1996 to March 1997 in a shallow tropical coastal lagoon on the southwest coast of India. Though temporal variations in all components were significant, spatial variabilities were not statistically significant. POC values range from 200 to 5690 mg C m³ h⁻¹, while primary production, chlorophyll a, and phaeophytin varied between 0.02 and 14.53 mg C m⁻³ h⁻¹, 0.87 and 23.11 mg m⁻³ and 3.02 and 30.581 mg m⁻³, respectively. Phytoplankton and zooplankton abundance varied from 0.01 to 655.5×10⁵ no m⁻³ and negligible to 7.08×10⁵ no m⁻³ respectively; secondary production from 10 to 490 mg C m⁻³ and SPM between 0.38 and 74.43×10⁴ mg m⁻³ during this study. Temporally, postmonsoon months were observed to have the highest concentrations of POC in the lagoon waters. The bulk of the POC pool in the lagoon was composed of secondary producers (72%), followed by chlorophyll a (21%), phaeophytin (7%) and suspended particulate matter of inorganic origin (< 0.1%).     

Environmental Assessment of Aromatic Hydrocarbons-Contaminated Sediments of the Mexican Salina Cruz Bay

Concentrations of total aromatic hydrocarbons and extractable organic matter in the water column and sediment were determined in samples collected in the course of the last 20 years from the Salina Cruz Harbor, México, to assess the degree of organic contamination. In sediments, organic compounds accumulate in shallow areas mostly associated with extractable organic matter and fine fractions. Calculated geocumulation index and enrichment factors suggest that contamination could be derived from anthropogenic activities attributed to harbor and ship scrapping activities, as well as transboundary source. Concentration of total aromatic hydrocarbons (as chrysene equivalents) ranged from 0.01 to 534 μg l⁻¹ in water, and from 0.10 to 2,160 μg g⁻¹ in sediments. Total aromatic concentration of 5 μg g⁻¹ is proposed as background concentration.     

Isoprene Emission from the Forest of Haryana State

Tropical and sub tropical regions are regarded as dominant source of biogenic volatile organic compounds emission (BVOC). However, measurement studies from these regions are limited and largely confined to South Africa and Amazonia. Consequently, global BVOC estimates are mainly based on modeling studies. Moreover, BVOC emission estimate is altogether lacking for any region of the Indian sub continent. This study attempts to estimate isoprene emission capacity of forest of Haryana state. Individual plant species isoprene emission capacity is found to vary from below detection limit (BDL) to 12.01 mg Cm^{− 2} h^{− 1}. Maximum emission capacity (12.01 mg Cm^{− 2} h^{− 1}) is noticed in case of Dalbergia sissoo. The area average isoprene emission capacity for the Haryana forest is found to be 19.98 mg Cm^{− 2} h^{− 1}, which is significantly (2.4 times) higher than the reported isoprene emission value of 8.2 mg Cm^{− 2} h^{− 1} for the Kalahari woodland of Africa.     

Eutrophication and Sedimentation Patterns in Complete Exploitation of Water Resources Scenarios: An Example from Northwestern Semi-arid Mexico

Water requirements to supply human needs lead water stakeholders to store more water during surplus periods to fulfil the demand during – not only – scarcity periods. At the reservoirs, mostly those in semi-arid regions, water level then fluctuates extremely between rises and downward during one single year. Besides of water management implications, changes on physical, chemical and biological dynamics of these drawdown and refilling are little known yet. This paper shows the results, throughout a year, on solids, nutrients (N and P), chlorophyll-a, and sedimentation changes on the dynamics, when the former policy was applied in a reservoir from the semi-arid Northwestern Mexico. Water level sinusoidal trend impinged changes on thermal stratification and mixing, modifying nutrient cycling and primary producer responses. According to nitrogen and phosphorus concentration as well as chlorophyll-a, reservoir was mesotrophic, becoming hypertrophic during drawdown. Nutrient concentrations were high (1.22 ± 0.70 and 0.14 ± 0.12 mg P l⁻¹), increasing phosphorus and lowering N:P significantly throughout the study period, although no intensive agricultural, no urban development, neither industrial activities take place in the watershed. This suggests nutrient recycling complex mechanisms, including nutrient release from the sediment–water interface as the main nutrient pathway when shallowness, at the same time as mineralization, increases. Outflows controlled nitrogen and phosphorus availability on the ecosystem while organic matter depended on river inflows. As on other subtropical aquatic ecosystems, nitrogen limited primary productivity (Spearman correlation R = 0.75) but chlorophyll-a seasonal pattern showed an irregular trend, prompting other no-nutrient related limitants. Shallowness induced a homogeneous temporal pattern on water quality. This observed temporal variability was mainly explained statistically by changes on solids (mineral and organic), chlorophyll-a and flows (62.3%). Annual sedimentation rates of total solids ranged from 11.73 to 16.29 kg m⁻² year⁻¹ with organic matter comprising around 30%. N:P ratio on sedimentation rates were as high as could be expected in a resuspension dominated ecosystem, and spatially inverse related with N:P ratio on bottom sediments. Distance from river inlet into the reservoir reveals a marked spatial heterogeneity on solid and nitrogen sedimentation, showing the system dependence on river inflows and supporting resuspension as the main phosphorus pathway. Accretion rates (2.19 ± 0.40 cm year⁻¹) were not related to hydrological variability but decreased with the distance to the river input. Total sediment accumulation (9,895 tons km⁻² year⁻¹) denotes siltation as other serious environmental problem in reservoirs but possibly not related with operational procedures.     

Butyltin Compounds in Sediments of the Bahía Blanca Estuary, Argentina

Systematic measurements of both Tributyltin (TBT) and Dibutyltin (DBT) in sediments along different locations in the inner zone of Bahía Blanca estuary were done. Two samples were taken near the main dry dock facility, at Puerto Belgrano naval base, in Argentina. TBT concentrations from non-detected to 170.3 ng Sn g⁻¹ were measured in the inner region of the estuary, and higher one of 3,288 ng Sn g⁻¹ near the dry dock at Puerto Belgrano. DBT values ranging between non-detected and 75.2 ng Sn g⁻¹ were obtained along the principal channel, but extreme concentration of 1,645 ng Sn g⁻¹ was measured at Puerto Belgrano. These values show that this estuary is affected by organotin pollution, mainly in areas of heavy shipyard activities.     

Spatial and Temporal Variations in Trace Metal Concentrations in the Cockle, Austrovenus Stutchburyi from Otago, New Zealand

This is the first comprehensive study of sources of variation in metal concentrations within the whole tissues of a shallow burrowing, filter-feeding intertidal clam, Austrovenus stutchburyi. Samples were collected from 12 sites in April, August, November and February in 1993–1994 in the vicinity of Otago Harbour and Peninsula, New Zealand. Total tissue trace metal concentrations (μg g⁻¹ dry weight) were measured in individual animals for the essential metals : Mn, Cu, Zn, Ni and the non-essential Cr using trace-metal clean acid-digestion and ICP-OAES techniques. Average metal concentrations were 3–60 μg g⁻¹ for Cu, 40–118 μg g⁻¹ for Zn, 2–12 μg g⁻¹ for Mn, 5–35 μg g⁻¹ for Ni and 1–44 μg g⁻¹ for Cr. These levels decreased with body weight and differed amongst sites except for Cr in February (mid-summer). Highest concentrations occurred at sites close to a city (Dunedin) and within the central harbour region although the Cu, Zn, Ni and Cr concentrations did not correlate with the environmental gradient or season. At one coastal site, samples of both the blue mussel Mytilus galloprovincialis and cockles gave similar trends in trace metal levels. These results suggest that the cockle could be a useful trace metal biomonitor within NZ estuaries.     

Selective and sensitive extractive spectrophotometric determination of micro amounts of palladium(II) in spiked samples: using a new reagent N-ethyl-3-carbazolecarbaxaledehydethiosemicarbazone

N-Ethyl-3-cabazolecarboxaldehydethiosemicarbazone (ECCT) is proposed as a new, sensitive and selective complexing reagent for the separation and extractive spectrophotometric determination of palladium(II) at pH: 4.0 to form a yellowish orange colored 1:1 chelate complex, which is very well extracted in to n-butanol. The absorbance was measured at a maximum wavelength, 410 nm. This method obeys Beer’s law in the concentration range 0.0–6.6 μg mL⁻¹ and the correlation coefficient of Pd(II)-ECCT complex is 0.998, which indicates an excellent linearity between the two variables with good molar absorptivity and Sandell’s sensitivity, 1.647 × 10⁴ l mol⁻¹cm⁻¹, 6.49 × 10⁻³ μg cm⁻², respectively. The instability constant of complex calculated from Edmond’s method, 2.724 × 10⁻⁵ was in good agreement with the value calculated from Asmus’ method 2.624 × 10⁻⁵, at room temperature. The precision and accuracy of the method is checked with calculation of relative standard deviation (n = 5), 0.839. Edmond’s method was observed to be a more selective method in the presence of EDTA, oxalate and phosphate ions. The method was successfully applied for the determination of Pd(II) in water samples, synthetic mixtures and hydrogenation catalysts, employing an atomic absorption spectrometer for comparing these results.     

Total Mercury Distribution in Different Tissues of Frigate Tuna (Auxis thazard thazard) from the Atlantic Coastal Waters of Ghana, Gulf of Guinea

Total mercury concentrations in different tissues of frigate tuna fish (Auxis thazard thazard) was determined by the cold vapour atomic absorption spectrometry technique using an automatic mercury analyzer. A mixture of HNO₃, HClO₄ and H₂SO₄ was used for complete oxidation of organic tissue. The concentration of mercury obtained was in the order Gills < Stomach < Gonads < Intestine < Heart < Duodenum < Liver < Muscle. The concentration of total mercury detected in the edible muscle tissue of the tuna fish tested ranged from 0.044 to 0.201 μg g⁻¹ (mean = 0.108 μg g⁻¹) wet weight. These levels are all within the maximum allowed/recommended level in fish (0.5 μg g⁻¹ wet weight) set by the Food and Agriculture Organisation/World Health Organisation (FAO/WHO) and are therefore unlikely to constitute any significant mercury exposure to the general population because of consumption of tuna fish. The results of the study suggest a relatively clean marine environment that has not been significantly impacted by mercury contamination probably due to minimal industrial activity in the region.     

Pollution by organochlorine pesticides in Navachiste-Macapule,Sinaloa, Mexico

The lagoon system of Navachiste-Macapule is located in northern Mexico, in the state of Sinaloa, with an area of 24,000 ha. The main economic activity in the area is agriculture, and the lagoon lies next to the irrigation district ID-063 which covers 116,615 ha. The purpose of this study is to evaluate the levels of pollution generated by organochlorine pesticides (OC) in the surface sediments of the lagoon and in the agricultural drains of the ID-063 that are supposedly transported into the system as a result of agricultural activities and runoff from adjacent land. For this, between 2006 and 2007, 45 surface sediment samples were collected (warm dry, rainy and cold dry) from 15 sampling sites, during the three climatic seasons. Of these, eight were located inside the lagoon in marine conditions (salinity >31 PSU) and seven in the agricultural drains of the ID-063 in freshwater conditions (salinity <5 PSU). The average concentration of the OC in the sediments was 44.75 ng g^− 1, among which the group of the alicyclic compounds presented the greatest concentrations. The average value of the total organic carbon (TOC) in the sediments of the system was 0.90%. The sediments collected inside the lagoon had an average OC concentration of 18.97 ng g^− 1, and the predominant type of sediment was fine to very fine sand. The average OC concentration in the sediments collected in the agricultural drains was 75.69 ng g^− 1, where fine sediments (silt) were predominant. The presence of methoxychlor, endrin and heptachlor suggested that these compounds were continuously used in the system, even though their use is forbidden in Mexico.