Total suspended matter observation in the Pearl River estuary from in situ and MERIS data

Based on the cruise data collected in the Pearl River estuary (PRE) in May 2008, an empirical two-band model by using the ratio of R _rs at 629 and 671 nm was established to retrieve total suspended matter (TSM) concentration with the determination coefficient (R²) of 0.854, mean relative error (MRE) of 7.483%, and root-mean-square error (RMSE) of 1.295 mg L^???1. To match with medium resolution imaging spectrometer (MERIS) bands, in situ remote sensing reflectance was re-sampled to the bandwidth of 10 nm. The relationship between TSM and re-sampled R _rs at 620 nm (MERIS band 6) and 665 nm (MERIS band 7) are obtained (R² = 0.748, RMSE = 1.697 mg L^???1, MRE = 8.785%, n = 13). Additionally, to map the spatial distribution of TSM in the PRE, MERIS level_1B data were calibrated using a multiple linear regression model based on in situ R _rs. Another dataset collected in the PRE in January 2004 was used to validate the two-band model and also applied to map TSM distribution from MERIS image. The comparison between measured TSM values and modeled ones showed satisfactory results (R² = 0.753, MRE = 22.199%, and RMSE = 2.603 mg L^???1).     

Arsenic accumulation in lichens of Mandav monuments, Dhar district, Madhya Pradesh, India

Total arsenic in four different growth forms of lichens growing on old monuments in the city of Mandav, Dhar district of Madhya Pradesh, India was analyzed. Among the different growth forms, foliose lichens were found to accumulate higher amounts of arsenic followed by leprose form. The squamulose and crustose form accumulates the lower concentration of arsenic and ranged between 0.46 ± 0.03 and 20.99 ± 0.58 μg g^???1 dry weight, while the foliose and leprose lichens have ranges from 10.98–51.95 and 28.63–51.20 μg g^???1 dry weight, respectively. The substrate having high arsenic ranges also exhibit higher ranges of arsenic on lichens growing on them. The cyanolichens exhibit higher concentration of arsenic than the green photobiont-containing squamulose form. The higher concentration of arsenic was found at site having past mining activities. LSD (1%) shows significant difference for As concentration in lichens thallus between the selected sites and species both.     

Water quality and bacteriology in an aquaculture facility equipped with a new aeration system

The HOBAS aeration system was tested to compare changes in environmental and bacteriological parameters in ponds growing Penaeus monodon during a single production cycle. The stocking density in the aerated pond was doubled to 12 post-larvae (PL) m^???2 in contrast to the non-aerated pond with 6 (PL) m^???2. Microbial abundance in the ponds ranged between 10^5???6 cells ml^???1. Among the physiological groups of bacteria enumerated, the heterotrophs dominated with an abundance of 10⁴ CFU ml^???1. Of the nitrogen and sulfur cycle bacteria, the nitrifiers flourished in the aerated pond and could maintain ammonia-N concentration within permissible levels. Bacterial activity also maintained sulfide concentrations at <?0.03 mg l^???1. Non-aerated conditions promoted denitrification maintaining nitrate concentration between 0.32 and 0.98 μM NO₃ ^???-N l^???1. However, a marked increase in ammonium content was observed in the non-aerated pond at the end of the culture period. Thus in high-density ponds, the aerators served to stimulate bacterial growth and activity which consequently maintained the quality of the water to match that of low-density ponds. Accordingly, these aerators could be effectively used to sustain higher yields. The effluent from the aerated pond is less likely to alter the redox balance of the receiving waters.     

Selenium in surface and irrigation water in the Kendrick irrigation district, Wyoming

High selenium (Se) concentrations have been found in surface waters in the Kendrick Reclamation Project, Wyoming. Precipitation and irrigation water moving over seleniferous soils are contributing causes, and drought may exacerbate this. This study surveyed Se concentrations and discharges in local surface streams, irrigation drains, and the delivery canal. Sites were sampled monthly and analyzed for Se and total suspended solids (TSS). A completely randomized design with two factors (soil parent material and location, inside or outside irrigation district) was used. Mean Se concentrations were 64 μg L^???1 inside the irrigation district on shale soils, 17 μg L^???1 inside the district off shale soils, 5 μg L^???1 outside the district on shale soils, and 3 μg L^???1 outside the district off shale soils. Correlations between discharge and Se concentrations were generally negative, while correlations between discharge and Se load were generally positive. There was little correlation between load and concentration, and little correlation between TSS and Se. A comparison of Se concentrations in streams and drains showed Se concentrations were significantly higher (p?<?0.001) in streams during the irrigation season, but not in the off-season (p?=?0.515). We conclude that higher discharges decrease Se concentration, but increase load. Conversion from flood to sprinkle irrigation may increase Se concentrations by reducing discharge, but decrease Se loads going into the N. Platte River, and will likely alter the timing and magnitude of flows. Both load and concentration should be considered when implementing Se regulations and standards.     

Occurrence of organochlorine pesticide residues in green mussel (Perna viridis L.) and water from Ennore creek, Chennai, India

Green mussel (Perna viridis) and water samples were collected from Ennore creek, Chennai by seasonal sampling and analyzed for organochlorine pesticide residues (OCPs) like dichloro-diphenyl-trichloroethane (DDT) and its metabolites, isomers of hexachlorocyclohexane (HCH) and endosulfan. These residues were analyzed by using gas chromatograph (GC) with μECD. In the present study, mussel samples showed very low concentrations of OCPs in the statistical order of DDT (5.83 ng g^???1 wet tissue) > endosulfan (2.84 ng g^???1 wet tissue) > HCH (2.34 ng g^???1 wet tissue). Concentrations of OCPs in water samples were in the statistical order of endosulfan (29.21 ng L^???1)?> HCH (17.14 ng L^???1)?> DDT (14.63 ng L^???1). To our knowledge, this is the first report on the seasonal variation of OCPs and especially the quantification of endosulfan in Ennore Creek. The present study recommends that continuous monitoring in Ennore creek is necessary to assess possible impact on human health.     

Removing arsenic from groundwater in Cambodia using high performance iron adsorbent

In Cambodia, groundwater has been contaminated with arsenic, and purification of the water is an urgent issue. From 2010 to 2012, an international collaborative project between Japan and Cambodia for developing arsenic-removing technology from well water was conducted and supported by the foundation of New Energy and Industrial Technology Development Organization, Japan. Quality of well water was surveyed in Kandal, Prey Veng, and Kampong Cham Provinces, and a monitoring trial of the arsenic removal equipment using our patented amorphous iron (hydr)oxide adsorbent was performed. Of the 37 wells surveyed, arsenic concentration of 24 exceeded the Cambodian guideline value (50 μg L^?1), and those of 27 exceeded the WHO guideline for drinking water (10 μg L^?1). Levels of arsenic were extremely high in some wells (>1,000–6,000 μg L^?1), suggesting that arsenic pollution of groundwater is serious in these areas. Based on the survey results, 16 arsenic removal equipments were installed in six schools, three temples, two health centers, four private houses, and one commune office. Over 10 months of monitoring, the average arsenic concentrations of the treated water were between 0 and 10 μg L^?1 at four locations, 10–50 μg L^?1 at eight locations, and >50 μg L^?1 at four locations. The arsenic removal rate ranged in 83.1–99.7 %, with an average of 93.8 %, indicating that the arsenic removal equipment greatly lower the risk of arsenic exposure to the residents. Results of the field trial showed that As concentration of the treated water could be reduced to <10 µg L^?1 by managing the As removal equipment properly, suggesting that the amorphous iron (hydr)oxide adsorbent has high adsorbing capacity for As not only in the laboratory environment but also in the field condition. This is one of the succeeding As removal techniques that could reduce As concentration of water below the WHO guideline value for As in situ.     

Multiple metal tolerance and biosorption of cadmium by Candida tropicalis isolated from industrial effluents: glutathione as detoxifying agent

The ability of cadmium uptake by metal-resistant yeast, Candida tropicalis, from the liquid medium and wastewater was evaluated. The minimum inhibitory concentration of Cd^2?+? against C. tropicalis was 2,500 mg L^???1. The yeast also showed tolerance toward Zn^2?+? (1,400 mg L^???1), Ni^2?+? (1,000 mg L^???1), Hg^2?+? (1,400 mg L^???1), Cu^2?+? (1,000 mg L^???1), Cr^6?+? (1,200 mg L^???1), and Pb^2?+? (1,000 mg L^???1). The yeast isolate showed typical growth curves, but lag and log phases extended in the presence of cadmium. The yeast isolate showed optimum growth at 30°C and pH 8. The metal processing ability of the isolate was determined in a medium containing 100 mg L^???1 of Cd^2?+?. C. tropicalis could decline Cd^2?+? 70%, 85%, and 92% from the medium after 48, 96, and 144 h, respectively. C. tropicalis was also able to remove Cd^2?+? 40% and 78% from the wastewater after 6 and 12 days, respectively. Cd produced an increase in glutathione (GSH) and nonprotein thiol levels by 135% and 134% at 100-mg L^???1 concentration, respectively. An increase in the synthesis of GSH is involved in metal tolerance, and the presence of increasing GSH concentrations may be a marker for high metal stress in C. tropicalis. C. tropicalis, which is resistant to heavy metal ions and is adaptable to the local environmental conditions, may be employed for metal detoxification operations.     

Distribution and chemical partitioning of heavy metals in marine near-shore sediment cores: a case study from the Xugou, Lianyungang, China

The concentrations and chemical partitioning of heavy metals (Co, Cr, Ni, Zn, Cu, and Pb) in the marine near-shore sediment cores were investigated. Typically, the mean concentrations from Core B sediment samples were 98.6, 21.1, 47.0, 46.4, 107.6, and 31.9 mg kg^???1 for Cr, Co, Ni, Cu, Zn, and Pb, respectively. The heavy metal concentrations were normalized to commonly used reference elements Al, Li, Sc, and total organic carbon. Based on Pearson coefficients, Li was found to be a good normalizer for Co (r?= 0.974), Cr (r?= 0.967), Ni (r?= 0.898), and Zn (r?= 0.929) in 80 sediment samples from three sampling sites. However, the correlation coefficients between Li and Cu, and Li and Pb were relatively low. Multivariate statistic approaches (Principal Component Analysis and Cluster Analysis) were adopted for data treatment, allowing the identification of two main factors controlling the heavy metal variability in the sediments. Heavy metals in the enrichment sections were evaluated by a sequential extraction method for possible chemical forms in sediments. The results showed that the residual, Fe/Mn oxides and Organic/sulfide fractions were dominant geochemical phases in the enriched sections, indicating low bioavailability of heavy metals in sediments.     

Seasonal perspective of dietary arsenic consumption and urine arsenic in an endemic population

Exposure to arsenic in arsenic endemic areas is most remarkable environmental health challenges. Although effects of arsenic contamination are well established, reports are unavailable on probable seasonal variation due to changes of food habit depending on winter and summer seasons, especially for endemic regions of Nadia district, West Bengal. Complete 24-h diets, drinking–cooking water, first morning voided urine samples, and diet history were analyzed on 25 volunteers in arsenic endemic Chakdah block of Nadia district, once in summer followed by once in winter from the same participants. Results depicted no seasonal variation of body weight and body mass index. Arsenic concentration of source drinking and cooking water decreased (p?=?0.04) from 26 μg L^?1 in summer to 6 μg L^?1 in winter season. We recorded a seasonal decrease of water intake in male (3.8 and 2.5 L day ^?1) and female (2.6 and 1.2 L day^?1) participants from summer to winter. Arsenic intake through drinking water decreased (p?=?0.04) in winter (29 μg day^?1) than in summer (100 μg day^?1), and urinary arsenic concentration decreased (p?=?0.018) in winter (41 μg L^?1) than in summer (69 μg L^?1). Dietary arsenic intake remained unchanged (p?=?0.24) over the seasons. Hence, we can infer that human health risk assessment from arsenic needs an insight over temporal scale.     

Arsenic and trace metals in river water and sediments from the southeast portion of the Iron Quadrangle, Brazil

The Iron Quadrangle has been one of the most important gold production regions in Brazil since the end of the seventeenth century. There, arsenic occurs in close association with sulfide-rich auriferous rocks. The most abundant sulfide minerals are pyrite and arsenopyrite, yet trace metal sulfides occur in subordinate phases as well. Historical mining activities have been responsible for the release of As and trace metals to both aquatic and terrestrial environments close to mining sites in the region. Therefore, this study was aimed to evaluate the distribution and mobility of As, Cd, Co, Cr, Cu, Ni, Pb, and Zn in streams in the southeast portion of the Iron Quadrangle between the municipalities of Ouro Preto and Mariana, the oldest Brazilian Au mining province. Total concentrations of some trace metals and arsenic in water were determined. The four-stage sequential extraction procedure proposed by the commission of the European Communities Bureau of Reference (BCR) was used to investigate the distribution of these elements in stream sediments. Arsenic concentration in water was >10 ??g L^???1 (maximum limit permitted by Brazilian environmental regulations for water destined for human consumption) at all sampling sites, varying between 36.7 and 68.3 ??g L^???1. Sequential extraction in sediments showed high concentrations of As and trace metals associated with easily mobilized fractions.     

UV/H2O2 oxidation of arsenic and terbuthylazine in drinking water

Arsenic is a widespread contaminant in the environment. The intake of water containing high concentrations of arsenic could have serious impact on human health, such as skin and lung cancer. In the European Union, thus, also in Italy, the arsenic limit in drinking water is 10 μg L^?1. Several water remediation treatment technologies are available for arsenic removal. For some processes, the removal efficiencies can be improved after an oxidation step. Most full-scale applications are based on conventional oxidation processes for chemical micropollutant removal. However, if water contains arsenic and refractory organic contaminants, the advanced oxidation processes could be considered. The aim of this work was to investigate the effectiveness of ultraviolet (UV) radiation alone and in combination with hydrogen peroxide for the oxidation of arsenic and terbuthylazine (TBA). The experimental tests were performed in groundwater at the laboratory scale (0.1 mg L^?1 As(III) and 10 μg L^?1 TBA). Hydrogen peroxide alone (15 mg L^?1) was ineffective on both arsenic and TBA oxidation; the 253.7-nm radiation alone did not oxidize arsenic(III), but photolyzed efficiently TBA (52 % removal yield at a UV dose of 1,200 mJ cm^?2). The UV/H₂O₂ advanced oxidation (UV dose 600–2,000 mJ cm^?2, 5–15 mg L^?1 H₂O₂) was the most effective process for the oxidation of both arsenic and TBA, with observed oxidation efficiencies of 85 and 94 %, respectively, with 5 mg L^?1 H₂O₂ and a UV dose of 2,000 mJ cm^?2.     

Spectrophotometric determination of platinum(IV) in alloys, complexes, environmental, and pharmaceutical samples using 4-[N,N-(diethyl)amino] benzaldehyde thiosemicarbazone

4-[N,N-(Diethyl)amino] benzaldehyde thiosemicarbazone (DEABT) is proposed as an analytical reagent for the spectrophotometric determination of platinum(IV). The DEABT forms 1:2 yellow complex with Pt(IV), which is sparingly soluble in water and completely soluble in water–ethanol–DMF medium. The Pt(IV)–DEABT complex shows maximum absorbance at 405 nm. Beer’s law is valid up to 7.80 μg cm^???3, and optimum concentration range for the determination of platinum(IV) is 0.48–7.02 μg cm^???3. The molar absorptivity and Sandell’s sensitivity of the method are found to be 1.755 × 10⁴ dm³ mol^???1 cm^???1 and 0.0012 μg cm^???2, respectively. The relative error and coefficient of variation (n?=?6) for the method does not exceed ±0.43% and 0.35%, respectively. Since the method tolerates a number of metal ions commonly associated with platinum, it can be employed for the determination of platinum in environmental samples, pharmaceutical samples, alloys, catalysts, and complexes. The method is rapid as the Pt(IV)–DEABT complex is soluble in water–ethanol–DMF medium and not requiring any time consuming extraction method for the complex.     

Metals in tissues of fish from Yelkoma Lagoon, northeastern Mediterranean

This study was performed to investigate the metal concentrations in muscle, liver, gonad, and gill of gilthead seabream (Sparus aurata L., 1758), European seabass (Dicentrarchus labrax L., 1758), and keeled mullet (Liza carinata Valenciennes, 1836) from Yelkoma Lagoon, northeastern Mediterranean region. So, the levels of cadmium, cobalt, chromium, copper, iron, manganese, nickel, lead, and zinc in tissues of specimens from the lagoon were determined by inductively coupled plasma optical emission spectrometer. Concentrations of metals in muscles of the examined species ranged from 0.10 to 0.47 mg kg^???1 for cadmium, 0.10 to 0.43 mg kg^???1 for cobalt, 0.17 to 0.72 mg kg^???1 for chromium, 0.62 to 1.03 mg kg^???1 for copper, 28.9 to 52.3 mg kg^???1 for iron, 0.75 to 0.96 mg kg^???1 for manganese, 0.11 to 0.57 mg kg^???1 for nickel, 0.19 to 0.47 mg kg^???1 for lead, and 6.01 to 13.9 mg kg^???1 for zinc, respectively. Additionally, metal concentrations in muscles of fish were assessed for human uses according to provisional tolerable weekly intake and provisional tolerable daily intake.     

Assessment of environmental radioactivity for Batman, Turkey

The province of Batman, located in southern Anatolia, has a population of approximately 500,000. To our knowledge, there exists no information regarding the environmental radioactivity in this province. Therefore, gamma activity measurements in soil, building materials and water samples and an indoor radon survey have been carried out in the Batman province. The mean activity concentrations of the natural radionuclides (²²⁶Ra, ²³²Th and ⁴⁰K) and a fission product (¹³⁷Cs) were 35 ± 8, 25 ± 10, 274 ± 167 and 12 ± 7 Bq kg^???1, respectively, in the soil samples. The concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K in the selected building materials ranged from 18 to 48 Bq kg^???1, 8 to 49 Bq kg^???1 and 68 to 477 Bq kg^???1, respectively. All the calculated radium equivalent (Ra_eq) activity values of the building material samples are lower than the limit of 370 Bq kg^???1, equivalent to a γ-dose of 1.5 mSv year^???1. The activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K in tap waters collected from the study area were determined with mean specific activity concentrations of 42 ± 15, 35 ± 9 and 524 ± 190 mBq L^???1, respectively. Indoor radon measurements were made at 95 dwellings in Batman using a CR-39 detector. The radon concentration levels were found to vary from 23 to 145 Bq m^???3. The arithmetic mean of the measured radon concentration levels was found to be 84 Bq m^???3 with a standard deviation value of 23 Bq m^???3. The measurement results obtained in this study did not significantly differ from those taken in other parts of the country. The data generated in this study can be used to determine whether the Batman province is in a normal or high background radiation area and provides a valuable database for future estimations of the impact of radioactive pollution.     

Silica glass modified with flavonoid derivatives for preconcentration of some toxic metal ions in water samples and their determination with ICP-MS

Quercetin (3,3^′,4^′,5,7-pentahydroxyflavone) chemically bonded through pyran rearrangement on modified controlled pore silica glass (QCPSG) with a capacity 0.213 mmol/g was used for solid phase extraction of some toxic metal and metalloid ions. The newly designed QCPSG quantitatively sorbs As(V), Cd(II), Hg(II), and Pb(II) at the pH range 7.5–8.5 after 10 min of stirring. HCl (1 mol L^???1) instantaneously elutes all the metal ions. The sorption capacity of the ion collector is 0.42, 0.46, 0.53, and 0.49 mmol g^???1 for As(V), Cd(II), Hg(II), and Pb(II), respectively, whereas the preconcentration factor is 200. The effect of NaCl, Na₂SO₄, NaF, NaBr, Na₃PO₄, and other interfering salts on the sorption of metal ions (50 μg L^???1) was reported. Analytical detection limits of As(V), Cd(II), Hg(II), and Pb(II) were 4.18, 2.44, 15.86, and 25.00 pg mL^???1, respectively. QCPSG was used in the separation of the investigated metal ions from some natural water samples collected from diverse origins followed by determination by inductively coupled plasma–mass spectrometry. The data were compared with those obtained by the standard methods of determination using atomic absorption (hydride generation, HGAAS and after solvent extraction with ammonium pyrolidine dithiocarbamate/methyl isobutyl ketone). The suggested solid phase extraction method was found accurate with no random error.     

Water chemistry influences the toxicity of silver to the green-lipped mussel Perna viridis

The study determined the influence and relative importance of water chemistry parameters (pH, alkalinity, hardness) on the acute toxicity of silver to the green mussel Perna viridis. A preliminary bioassay revealed that 4 mg L^???1 of silver caused 50% mortality (LC₅₀) in 96 h for mussels placed in seawater with pH 8.5, hardness 1,872 mg L^???1, and alkalinity 172 mg L^???1. Mortality of mussels increased with decreasing pH and increasing hardness and alkalinity variables. In contrast the mortality decreased with increasing pH and decreasing hardness and alkalinity values. The water chemistry also affected the concentration of sliver in experimental seawater and bioaccumulation of silver in mussels. The results revealed that the chemical properties of seawater must be considered while conducting toxicity tests with metals like silver. The possible explanations for the influence of water chemistry on silver toxicity to P. viridis are discussed.     

Estimation of shipping emissions in Candarli Gulf, Turkey

Ships are significant air pollution sources as their high powered main engines often use heavy fuels. The major atmospheric components emitted are nitrogen oxides, particulate matter (PM), sulfur oxide gases, carbon oxides, and toxic air pollutants. Shipping emissions cause severe impacts on health and environment. These effects of emissions are emerged especially in territorial waters, inland seas, canals, straits, bays, and port regions. Candarli Gulf is one of the major industrial regions on the Aegean side of Turkey. The marine environment of the region is affected by emissions from ships calling to ten different ports. In this study, NO _x , SO₂, CO₂, hydrocarbons (HC), and PM emissions from 7,520 ships are estimated during the year of 2007. These emissions are classified regarding operation modes and types of ships. Annual shipping emissions are estimated as 631.2 t year^???1 for NO _x , 573.6 t year^???1 for SO₂, 33,848.9 t year^???1 for CO₂, 32.3 t year^???1 for HC, and 57.4 t year^???1 for PM.     

Assessment of trace metal concentration in feathers of seabird (Larus dominicanus) sampled in the Florianópolis, SC, Brazilian coast

Cd, Co, Cr, Cu, Mn, Ni, Zn, and Pb were measured in feather samples of adult, subadult, and juvenile of Larus dominicanus, sampled in the Florianólis, SC, in the south of Brazil in December 2005, by flame atomic absorption spectrophotometry. The average of the distribution of Cd concentration in adult feathers (0.072 μg g^???1) was significantly different than that found in juvenile feathers (0.021 μg g^???1). Cu concentration averages were not significantly different between adults (13.30 μg g^???1), subadults (9.67 μg g^???1), and juveniles (13.76 μg g^???1). For adults and juveniles there was significant difference in feather concentrations for Cd, Co, Cr, Ni, and Pb. The distribution of Mn concentration averages in feathers differs between adults (11.36 μg g^???1) and juveniles (1.184 μg g^???1). Ni concentration averages of adults (5.92 μg g^???1) were significantly higher than those of juveniles (2.23 μg g^???1). For Pb, concentration averages were significantly higher in adults (7.53 μg g^???1) than in juveniles (1.47 μg g^???1). The concentration of Co and Cr in juvenile and subadults are statistically different when compared with the adults. In the present study, levels of Cd, Co, Cr, Mn, Ni, Zn, and Pb increased with age. The concentrations of essential trace elements in L. dominicanus were generally comparable to values reported in other studies. With non-essential metals (Cd, Pb, and Ni), in our study, L. dominicanus had lower values than those reported for their northern Atlantic counterparts.     

A complex investigation of the extent of pollution in sediments of the Sava River. Part 1: Selected elements

The Sava River is the biggest tributary to the Danube River. As a part of the 6th FW EU project, Sava River Basin: Sustainable Use, Management and Protection of Resources (SARIB), ecological status of sediments was investigated. In order to assess the geographical distribution in sediment contamination of the Sava River, inorganic and persistent organic pollutants were analyzed in sediments at 20 selected sampling sites along the Sava River from its spring to its outfall into the Danube River. For comparability of data to other river basins the sediment fraction below 63 μm was studied. Due to complexity of the work performed, the results are published separately (“Part I: Selected elements” and “Part II: Persistent organic pollutants”). In the present study, the extent of pollution was estimated by determination of the total element concentrations and by the identification of the most hazardous highly mobile element fractions and anthropogenic inputs of elements to sediments. To assess the mobile metal fraction extraction in 0.11 mol L^???1, acetic acid was performed (first step of the Community Bureau of Reference extraction procedure), while anthropogenic inputs of elements were estimated on the basis of normalization to aluminum (Al) concentration. According to the Water Framework Directive, the following elements were investigated in sediments: cadmium (Cd), lead (Pb), nickel (Ni), and mercury (Hg). Furthermore, copper (Cu), zinc (Zn), chromium (Cr), arsenic (As), and phosphorous (P) were determined. The analyses of sediments demonstrated slightly elevated values for Hg, Cr, and Ni in industrially exposed sites (concentrations up to 0.6, 380, and 210 mg kg^???1, respectively). However, the latter two elements exist in sparingly soluble forms and therefore do not represent an environmental burden. P concentrations were found in elevated concentrations at agricultural areas and big cities (up to 1,000 mg kg^???1).     

A regional algorithm to model mesozooplankton biomass along the southwestern Bay of Bengal

A three-dimensional regression analysis attempted to model mesozooplankton (MSP) biomass using sea surface temperature (SST) and chlorophyll-a (Chl-a). The study was carried out from January 2014 to July 2015 in the southwestern Bay of Bengal (BoB) and sampling was carried out on board Sagar Manjusha and Sagar Purvi. SST ranged from 26.2 to 33.1 °C while Chl-a varied from 0.04 to 6.09 μg L^?1. During the course of the study period, there was a weak correlation (r?= 0.32) between SST and Chl-a statistically. MSP biomass varied from 0.42 to 9.63 mg C m^?3 and inversely related with SST. Two kinds of approaches were adopted to develop the model by grouping seasonal datasets (four seasonal algorithms) and comprising all datasets (one annual algorithm). Among the four functions used (linear, paraboloid, the Lorentzian and the Gaussian functions), paraboloid model was best suited. The best seasonal and annual algorithms were applied in the synchronous MODIS-derived SST and Chl-a data to estimate the MSP biomass in the southwestern BoB. The modelled MSP biomass was validated with field MSP biomass and the result was statistically significant, showing maximum regression coefficient for the seasonal algorithms (R²?=?0.60; p?=?0.627; α?= 0.05), than the annual algorithm (R²?=?0.52; p?=?0.015, α?=?0.05).