Enhancement of nickel biosorption on fungal biomass by enzymatic and alkali pretreatments

Enzymatic and alkali pretreatments were employed to improve nickel biosorption capacity of Rhizomucor pusillus biomass. Pretreatment with 0.002–80 g l^?1 NaOH and 0.0001–0.1 Anson Unit (AU) g^?1 protease enhanced the biosorption capacity of fungal biomass. Increasing the concentration of NaOH from 0.002 to 5 g l^?1 improved nickel removal from 93.2 to 100.0 % while untreated biomass showed 64.6 % Ni(II) removal. Pretreatment with higher concentrations of NaOH, 5–80 g l^?1 resulted in nearly complete removal of nickel ions. Pretreatment of the biomass with 0.0001 AU g^?1 protease improved the nickel removal to over 91 %, while increasing the enzyme loading to 0.1 AU g^?1 improved the removal to 93 %. Untreated biomass removed 78.4, 63.0, and 96.3 % of chromium, copper, and lead ions, respectively, from a mixture solution of the ions. Respective metal removals were increased to 100, 98.9, and 100 % after pretreatment with 0.2 g l^?1 NaOH solution and to 87.8, 86.7, and 100 % after the enzymatic pretreatment with 0.1 AU g^?1 protease. Scanning electron microscopy analysis indicated that alkali and enzymatic pretreatments enhanced the porosity of the biomass. Furthermore, compositional analysis showed that both of the pretreatments removed a major part of fungal proteins (2.1–95.8 % removal). Glucosamine, N-acetyl glucosamine, and phosphates were the major ingredients of the pretreated biomass.     

Chemical characterization and sources of PM2.5 at 12-h resolution in Guiyang,China

The increasing emission of primary and gaseous precursors of secondarily formed atmospheric particulate matter due to continuing industrial development and urbanization are leading to an increased public awareness of environmental issues and human health risks in China. As part of a pilot study, 12-h integrated fine fraction particulate matter (PM_2.5) filter samples were collected to chemically characterize and investigate the sources of ambient particulate matter in Guiyang City, Guizhou Province, southwestern China. Results showed that the 12-h integrated PM_2.5 concentrations exhibited a daytime average of 51 ± 22 µg m^?3 (mean ± standard deviation) with a range of 17–128 µg m^?3 and a nighttime average of 55 ± 32 µg m^?3 with a range of 4–186 µg m^?3. The 24-h integrated PM_2.5 concentrations varied from 15 to 157 µg m^?3, with a mean value of 53 ± 25 µg m^?3, which exceeded the 24-h PM_2.5 standard of 35 µg m^?3 set by USEPA, but was below the standard of 75 µg m^?3, set by China Ministry of Environmental Protection. Energy-dispersive X-ray fluorescence spectrometry (XRF) was applied to determine PM_2.5 chemical element concentrations. The order of concentrations of heavy metals in PM_2.5 were iron (Fe) > zinc (Zn) > manganese (Mn) > lead (Pb) > arsenic (As) > chromium (Cr). The total concentration of 18 chemical elements was 13 ± 2 µg m^?3, accounting for 25% in PM_2.5, which is comparable to other major cities in China, but much higher than cities outside of China.     

Biotransformation potential of hexavalent chromium by Bacillus pumilus-S4, Pseudomonas doudoroffii-S5 and Exiguobacterium-S8 in association with hydrophytes

Three chromium-resistant bacteria Bacillus pumilus-S4, Pseudomonas doudoroffii-S5 and Exiguobacterium-S8 were isolated from chromium-contaminated wastewater/soil and could resist very high concentrations of potassium chromate in Luria agar (up to 25 mg ml^?1) and acetate minimal medium (2 mg ml^?1). The strains showed growth at diverse pH and temperatures and could resist multiple heavy metals. Pseudomonas doudoroffii-S5 reduced (8.27 mg hexavalent chromium 24 h^?1) at a lower initial potassium chromate concentration (100 μg ml^?1), but overall more chromate (28.4 mg hexavalent chromium 24 h^?1) was reduced at a higher initial concentration (1,000 μg ml^?1). The addition of various heavy metals (zinc sulphate, copper sulphate, and manganese sulphate at 50 μg ml^?1) in the chromium reduction media did not significantly affect the hexavalent chromium reduction potential of these isolates. The chromium removal/detoxification potential of these strains increased when used in conjunction with hydrophytes Eichornia crassipes and Pistia stratiotes. Interestingly, the whole process runs automatically with less energy input, that is, the bacterial strains support the growth of plant while in turn the plant releases exudates that help bacterial growth.     

Fast,green and effective chromium bio-speciation using <Emphasis Type="Italic">Sepia pharaonis</Emphasis> endoskeleton nano-powder

The development of a fast, effective, simple and low-cost procedure for chromium speciation is an analytical challenge. In this work, a new and simple method for speciation and determination of chromium species in different matrices was developed. Sepia pharaonis endoskeleton nano-powder was used as an adsorbent for the dispersive micro-solid-phase extraction. Finally, the desorbed chromium was determined using a graphite furnace atomic absorption spectrometer. The experimental results showed that Cr(III) could be quantitatively extracted by the adsorbent, while Cr(VI) adsorption was negligible. Concentrated H₂SO₄ and ethanol reduced Cr(VI)–Cr(III), and total chromium content was assessed as Cr(III). Then, the Cr(VI) concentration in the sample was calculated as the difference. The optimum conditions were obtained in terms of pH, adsorbent amount, contact time, and type, concentration and volume of eluent. Under the optimum conditions that involved the speciation of chromium ions from 25 mL of the water samples at pH 7.0 using 0.025 g of the adsorbent with contact time of 5 min, the method was validated in terms of linearity, precision and accuracy. The calibration curve was linear over the concentration range of 0.01–25.00 μg L^?1 for Cr(III). The obtained limit of detection for the proposed method was 0.003 µg L^?1. The maximum adsorption capacity of the adsorbent was found to be 995.57 mg g^?1. The proposed method was validated by the speciation of Cr(III) and Cr(VI) in different real water and wastewater samples with satisfactory results.     

Optimization and design of a continuous biosorption process using brown algae and chitosan/PVA nano-fiber membrane for removal of nickel by a new biosorbent

In this study, nickel ions adsorption from zinc ingot factory wastewater by brown algae (Sargassum glaucescens) and chitosan/polyvinyl alcohol nano-fiber membrane at continuous system was studied. The continuous process included a biosorption reactor and fixed-bed reactor that were optimized by predicting two batch steps with response surface modeling, based on the Box–Behnken in the novel approach. Nano-biosorbent characterized by scanning electron microscopy, Brunauer–Emmett–Teller and Fourier transform infrared spectrometer analysis. Maximum biosorption in this continuous system was at pH 6, biosorbent doses 8 g L^?1 S. glaucescens and 0.48 g L^?1 nano-fiber. The study of the reaction rate showed kinetic data best fitted by pseudo-first-order model with R ² > 0.95 than pseudo-second-order and intraparticle diffusion models. Biosorption equilibrium data were performed using Langmuir isotherm and Freundlich isotherm, Langmuir isotherm fit better with equilibrium data.     

Assessment of heavy metals in sediment and in suspended particles affected by multiple anthropogenic contributions in harbours

La Goulette, Rades and Sidi Bou Said harbours are considered as the most important commercial and tourist ports in the Gulf of Tunis. They are located on the northeast coast of Tunis and receive industrial and municipal wastewaters from Tunis city. The contamination level of copper, lead, zinc, cadmium, manganese, iron, total nitrogen and total organic carbon in the surface sediments was assessed on the basis of the enrichment index factors and corresponding to sediment quality guidelines. The results revealed moderate to highly elevated concentrations near to the sites of intense industrial, shipping and/or commercial activities suggesting a direct influence of these sources. In winter and summer, concentrations varied for cadmium, 0.28–1.40 mg kg^?1; lead, 18–217 mg kg^?1; zinc, 87–459 mg kg^?1; copper, 8–121 mg kg^?1; manganese, 208–254 mg kg^?1; and for iron, 24–40 g kg^?1. Furthermore, in summer the concentration of the total organic carbon and the total nitrogen contents range between 4.3–6.5 % and 0.06–0.49 % with an average value of 5.9 and 0.15 %, respectively. Whereas, in winter, total organic carbon and the total nitrogen concentrations varied between 2.3–9.6 % and 0.03–0.22 % with an average value of 6.1 and 0.14 %, respectively. The levels of lead, copper, zinc and iron in suspended particulate matter content range between 3.1–27.5 mg kg^?1; 0.4–11.7 mg kg^?1; 1–1.5 mg kg^?1; 1.2–1.7 g kg^?1, respectively. This study revealed that heavy metals pollution is mainly localized in the commercial (Rades) and fishing (La Goulette) harbours and not in the yachting (Sidi Bou Said) harbour.     

An easy and fast IC-CL procedure for the monitoring of Cu(II) and Co(II) in environmental samples

A luminol chemiluminescence (CL) detection/flow injection analysis technique coupled with ion chromatography (IC) has been employed for the determination of low levels of Cu(II) and Co(II) in drinking water samples. The detection system was the CL of luminol/perborate or luminol/percarbonate in alkaline medium catalyzed by these transition metals. Oxalic acid in a solution of KOH and N(CH₃)₄OH was used as an eluent in the IC to improve the column selectivity (Dionex CS5A). Concentration and pH of the eluent affected simultaneously the CL intensity and the retention times (t _R). Under the elution conditions used here, the retention times of both metal ions were much greater when the concentration of oxalic acid was decreased. Thus, R _t(_Cu) = 2.15 min and t _R(_Co) = 4.50 min were measured at 80 mM oxalic acid concentration, while t _R raised to 4.12 and 18 min for Cu(II) and Co(II), respectively, using a 10-mM concentration, but on the other hand, the CL signals showed substantially higher values when the concentration of oxalic acid was lesser in the eluent. An optimum oxalic acid concentration of 20 mM and an eluent pH = 4.7 were selected in order to have reproducible signals with a total analysis time of 10 min. The optimum flow rate for the mobile phase was 1.5 mL min^?1. The concentration and pH of the postcolumn reagents also affected the CL signal, obtaining optimum concentrations of 5 mM for both oxidants (perborate or percarbonate) and luminol, this last dissolved in a 0.1-M borate buffer at pH 12. The optimum flow rate for the postcolumn reagents was 1 mL min^?1. Linear calibrations for both transition metal ions were established, with calculated detection limits of 0.15 ng mL^?1 for Co(II) and 0.20 μg mL^?1 for Cu(II). Others ions commonly present in natural waters showed little or no interference. The method was successfully applied to water samples spiked with Cu(II) and Co(II), obtaining recoveries in the range of 85–128%, depending on the metal concentrations.     

Kinetic and equilibrium studies on the removal of <Superscript>14</Superscript>C-ethion residues from wastewater by copper-based metal–organic framework

There are compelling economic and environmental reasons to remove pesticides from wastewater because they are toxic and carcinogenic. The effectiveness of copper-based metal–organic framework (Cu-BTC) for adsorbing the insecticide ¹⁴C-ethion from wastewater has been studied as function of contact time, adsorbent dosage, temperature and pH. ¹⁴C-ethion/Cu-BTC isotherms exhibit two plateaus (BET type IV) and are reliably represented by Brunauer–Deming–Deming–Teller and Zhu–Gu models, with deviations of only 1.99 and 3.95%, respectively. The removal curve measured under batch operation is well represented by a pseudo-first-order equation, yielding results equivalent to the theoretical linear driving force model of Glueckauf. At pH 7, 75 mg L^?1 ethion concentration, 150 min, 25 °C and 0.425 g L^?1 Cu-BTC dose, the sorbent capacity is ca. 122 mg g^?1. Moreover, Cu-BTC has a good stability after six adsorptions cycles. Finally, our results disclose the fundamental understanding of the adsorption mechanism: the ethion molecule coordinates to two copper(II) atoms across the metal–organic framework channel via the phosphoryl (P–O) group.     

A comparison of metallic contents in lichen Pyxine subcinerea, its substratum and soil

Chromium, copper, cadmium, lead, nickel, iron and zinc contents of a lichen species (Pyxine subcinerea Stirton) and mango bark collected from 12 sites in Haridwar city (Uttarakhand) were compared with soil, sampled from beneath the tree from which lichens were collected. The metal contents in lichen, bark and soil ranged from 1,573 to 18,793, 256 to 590 and 684 to 801 μg g^?1, respectively. This clearly indicates that lichens accumulated higher amounts of metal compared to bark or soil. Statistical analysis revealed that metal concentration in lichens did not show significant linear correlation with the bark or soil. Pearsons correlation coefficients revealed negative correlation of Pb (r = ?0.2245) and Ni (r = ?0.0480) content between lichen and soil, which indicate direct atmospheric input of metals from ambient environment. Quantification and comparison of elemental concentration in lichens, its substratum and soil can provide valuable information about air quality in the collection area.     

Biodegradation of diazinon by the <Emphasis Type="Italic">Stenotrophomonas maltophilia</Emphasis> PS: pesticide dissipation kinetics and breakdown characterization using FTIR

A diazinon-degrading bacterium was isolated from paddy soils under flooded conditions. Biochemical characterization and 16S rRNA sequencing showed the isolate was an oxidase-positive Stenotrophomonas maltophilia. The isolate could grow on a mineral salt medium (MSM) supplemented with diazinon as the main carbon source (50 µg ml^?1) and dissipate the pesticide in a simple first-order manner with DT₅₀ and DT₉₀ of 4.54 and 15.09 days, respectively. The addition of glucose favored the bacterial growth and reduced the pesticide’s DT₅₀ and DT₉₀ to 3.39 and 11.27 days, respectively. The dissipation of diazinon in MSM was accompanied by a slight reduction of the pH which was more significant in the glucose-treated media. FTIR analysis proved the separation of the heterocyclic leaving group by hydrolyzing the ester bond and aerobic cleavage of the aromatic ring as the main pathways of diazinon degradation in the MSM. The dissipation of diazinon (150 µg g^?1) in the inoculated sterilized flooded paddy soils was biphasic, and based on this, only 31.55 µg g^?1 of the initial concentration declined with a faster rate while the rest of the residue dissipated slowly as the adsorbed phase. In the non-inoculated non-sterilized soils, diazinon dissipated more slowly with an initial lag phase.     

Phosphorus Budget of the Sundarban Mangrove Ecosystem: Box Model Approach

Phosphorus (P) cycling in mangroves plays an important role in productivity but the magnitude of atmospheric input in the mangrove P budget is still uncertain. This study applied a box model approach to assess P budget in the Indian Sundarban, the world’s largest mangrove ecosystem for conceptual understanding of P cycling and for better representation of transport and transformation of P within the mangrove ecosystem. The P content in the sediment (0.19–0.67 μg g^?1) was found much below its maximum retention capacity (322 μg g^?1) and was lower than the mean marine sediment (669 μg g^?1). The C:N and C:P ratios were correlated (r ² = 0.66, P < 0.01) and the major fraction of available P was recycled within the organic structure of mangrove ecosystem, thus maintaining productivity through conservation strategies. Atmospheric input accounted for 56.7% of total P input (16.06 Gg year^?1) and 50% of total P output (14.7 Gg year^?1) was attributed to plant uptake. Budget closing or unaccounted P (1.36 Gg) was only 8.5% of the total input. Two feedback pathways, i.e., input of P from dust fallout and biochemical mineralization of organic matter, significantly affected P availability. The findings of the study suggest that atmospheric deposition is of major importance as a natural and/or anthropogenic forcing function in the Sundarban mangrove system.     

Adsorption of lead, zinc and cadmium ions from contaminated water onto Peganum harmala seeds as biosorbent

Peganum harmala seeds were assessed as biosorbent for removing Pb²⁺, Zn²⁺and Cd²⁺ ions from aqueous solutions. The effects of various parameters such as the aqueous solution pH, the contact time, the initial metal concentration and the amount of adsorbent in the process were investigated. The adsorption efficiencies increased with pH. It was found that about 95 % of lead, 75 % of zinc and 90 % of cadmium ions could be removed from 45 ml of aqueous solution containing 20 mg l^?1 of each cation with 2 g of adsorbent at pH 4.5 after 15 min. The quantitative desorption of cadmium from adsorbent surface was achieved using 10 ml of a 0.5 M nitric acid solution. This condition was attained for lead and zinc ions with 10 ml of 1 M hydrochloric acid solution. Kinetic investigation of the process was performed by considering a pseudo-second-order model. This model predicts the chemisorption mechanism of the process. Langmuir, Freundlich, Temkin and Dubinin–Radushkevich models were tested for describing the equilibrium data. It was found that the Freundlich model describes the experimental data resulting from the adsorption of lead ions. However for cadmium and zinc ions, the adsorption equilibria were interpreted with the Langmuir model.     

Exploring the diverse potentials of <Emphasis Type="Italic">Planococcus</Emphasis> sp. TRC1 for the deconstruction of recalcitrant kraft lignin

Kraft lignin (KL) is the chief contaminant which is responsible for dark coloration, toxicity and high chemical oxygen demand (COD) of paper pulp mill effluent. The present study investigated the diverse potentials of Planococcus sp. TRC1 in the biodegradation of KL. Preliminary evaluation indicated that the strain was able to grow on broad spectrum of lignin-derived compounds, decolorize lignin-mimicking dyes and catabolize substrates of ligninolytic enzymes. Response surface methodology (RSM) was executed to perform the optimization of different process parameters. The results displayed that Planococcus sp. TRC1 could completely utilize 100 mg L^?1 of KL and 78% of 200 mg L^?1 of KL as sole source of carbon with concurrent reduction in COD and color. The biokinetic details of KL biodegradation showed that the values of \(\mu^{*}\), µ _max, \(q^{*}\) and q _max were 0.018 h^?1, 0.01 h^?1, 0.023 g g^?1 h^?1 and 0.05 g g^?1 h^?1, respectively. UV–visible spectrophotometry, SEM and FTIR indicated the significant alterations in the surface morphology, functional groups and chromophores during the course of biodegradation. XRD revealed the emergence of peak signifying the formation of low molecular weight intermediates after bacterial treatment. Considering the environmental impact, bacterial-treated KL illustrated less phytotoxicity using Vigna radiata seed bioassay. These results suggested that Planococcus sp. TRC1 could be a promising strain for the degradation of KL in an ecofriendly way.     

High-resolution profiles of iron, manganese, cobalt, cadmium, copper and zinc in the pore water of estuarine sediment

The remobilization of iron, manganese, cobalt, cadmium, copper and zinc in the pore water of estuarine sediment cores at Yingkou was assessed using diffusive equilibrium in thin films and diffusive gradients in thin films techniques. A relatively anoxic system (+33.7 to ?224.1 mV) in the sediment cores might cause the reductive release of iron, manganese and cobalt into pore water from the estuarine sediment. High-average concentrations of iron (47.85 μg ml^?1) and manganese (3.81 μg ml^?1) were observed using diffusive equilibrium in thin films on the sediment core, but the concentration of cobalt (18.02 ng ml^?1) was relatively low. A strong correlation between iron and cobalt was observed based on the vertical profiles of the metals. Manganese and iron were more readily released from the solid phase to the solution. The peak cobalt, copper and zinc concentrations were observed in the upper layer (2–4 cm) measured using diffusive gradients in thin films. However, the peak iron, manganese and cobalt concentrations were located in the deeper layer (≥7 cm). In addition, the concentration profiles measured using diffusive gradients in thin films of cobalt, copper and zinc were independent of the iron, manganese and cobalt distribution with respect to depth.     

Induced degradation of crude oil mediated by microbial augmentation and bulking agents

Different bacterial and fungal strains, isolated from petroleum hydrocarbon-contaminated soil, were tested, in isolation as well as in combination, for their ability to degrade total petroleum hydrocarbon (TPH) in soil samples spiked with crude oil (2, 5 or 10 %, w/w) for 30 days. The selected combination of bacterial and fungal isolates, i.e., Pseudomonas stutzeri BP10 and Aspergillus niger PS9, exhibited the highest efficiency of TPH degradation (46.7 %) in soil spiked with 2 % crude oil under control condition. Further, when this combination was applied under natural condition in soil spiked with 2 % (w/w) crude oil along with inorganic fertilizers (NPK) and different bulking agents such as rice husk, sugarcane, vermicompost or coconut coir, the percent degradation of TPH was found to be maximum (82.3 %) due to the presence of inorganic fertilizers and rice husk as bulking agent. Further, results showed that the presence of NPK and bulking agents induced the activity of degradative enzymes, such as catalase (0.718 m mol H₂O₂ g^?1), laccase (0.77 µmol g^?1), dehydrogenase (37.5 µg g^?1 h^?1), catechol 1, 2 dioxygenase (276.11 µ mol g^?1) and catechol 2, 3 dioxygenase (15.15 µ mol g^?1) as compared to control (without bioaugmentation). It was inferred that the selected combination microbes along with biostimulants could accentuate the crude oil degradation as evident from the biostimulant-induced enhanced activity of degradative enzymes.     

Evaluation of trace element concentration (acid leachable) in sediments from River Pánuco and its adjacent lagoon areas, NE México

A set of forty-one surface sediment samples were collected in River Pánuco and its adjoining lagoon areas in NE Mexico to identify the enrichment pattern of trace elements. The samples were analyzed for sediment texture, carbonates, organic carbon and acid leachable trace elements (ALTEs) using autoclave method [Fe, Mn, Cr, Cu, Ni, Co, Pb, Zn, Cd, V, Be, Ba, Sr, As]. Geochemical results of Fe, Cr, Ni, Co, V and Sr in zone 1 indicate that erosion in the upland region (Sierra Madre Oriental Mountains) is very high. The above feature is supported by the supremacy of finer sediments (82.12 %), carbonates (44.67 %) and organic carbon (10.74 %), which are brought down from the drainage basin. The overall average concentration of ALTEs Mn (607 μg g^?1), Cu (28.29 μg g^?1), Ni (16.56 μg g^?1), Pb (46.11 μg g^?1), Cd (1.81 μg g^?1) and Zn (92.18 μg g^?1) indicates higher values than the lowest effect level (LEL) and effects range low (ERL) of environmental indicators. The results suggest that they are due to the increase in oil refineries, metal based industries, shipping activities and the effluent input which could enter the biological cycle and might create human health problems.     

Significance of co-immobilized activated carbon and Bacillus subtilis on removal of Cr(VI) from aqueous solutions

Batch sorption system using co-immobilized (activated carbon and Bacillus subtilis) beads as adsorbent was investigated to remove Cr(VI) from aqueous solution. Fourier transform infrared spectroscopy analysis showed the functional groups of both bacteria and activated carbon in co-immobilized beads. Experiments were carried out as a function of contact time (5–300 min), initial metal concentration (50–200 mg L^?1), pH (2–8), and adsorbent dose (0.2–1 g L^?1). The maximum percentage of removal was found to be 99 %. Langmuir model showed satisfactory fit to the equilibrium adsorption data of co-immobilized beads. The kinetics of the adsorption followed pseudo-second-order rate expression, which demonstrates that chemisorption plays a significant role in the adsorption mechanism. The significant shift in the Fourier transform infrared spectroscopy peaks and a Cr peak in the scanning electron microscope–energy dispersive spectroscopy spectra further confirmed the adsorption. The results indicate that co-immobilized beads can be used as an effective adsorbent for the removal of Cr(VI) from the aqueous solution.     

Role of rhizosphere and soil properties for the phytomanagement of a salt marsh polluted by mining wastes

The goal of this study was to evaluate the soil properties and their modifications within the rhizosphere of spontaneous vegetation as key factors to assess the phytomanagement of a salt marsh polluted by mining wastes. A field survey was performed based on a plot sampling design. The results provided by the analyses of rhizospheric soil (pH, electrical conductivity (EC), organic carbon, total nitrogen, etc.) and metal(loid)s’ phytoavailability (assessed by EDTA) were discussed and related to plant metal uptake. The averages of pH and EC values of the bulk soil and rhizospheric samples were in the range of neutral to slightly alkaline (pH 7–8) to saline (>2 dS m^?1), respectively. Heavy metal and As concentrations (e.g. ~600 mg kg^?1 As, ~50 mg kg^?1 Cd, ~11,000 mg kg^?1 Pb) were higher in the rhizosphere for both total and EDTA-extractable fraction. Phragmites australis uptaked the highest concentrations in roots (e.g. ~66 mg kg^?1 As, ~1,770 mg kg^?1 Zn) but not in shoots, for which most of plant species showed low values for Zn (<300 mg kg^?1) but not for Cd (>0.5 mg kg^?1) or Pb (~20–40 mg kg^?1). Vegetation distribution in the studied salt marsh looked to be more affected by salinity than by metal pollution. The free availability of water for plants and the incoming nutrient-enriched effluents which flow through the salt marsh may have hindered the metal(loid)s’ phytotoxicity. The phytomanagement of these polluted areas employing the spontaneous vegetation is a good option in order to improve the ecological indicators and to prevent the transport of pollutants to nearby areas.     

Trace metal concentrations in euryhaline fish species from Chilika lagoon: human health risk assessment

Five trace metals, viz. copper (Cu), chromium (Cr), iron (Fe), mercury (Hg) and zinc (Zn), in three organs (muscle, gills and liver) of four selected fish species (Mugil cephalus, Eleutheronema tetradactylum, Etroplus suratensis and Daysciaena albida) from Chilika lagoon were studied monthly to assess the concentration level and human health risk via consumption. The average and range of metal concentrations (μg g^?1) in flesh of the fish species were found to be: Cu (4.15, 3.47–5.03), Cr (0.25, 0.04–0.63), Fe (19.72, 14.51–27.30), Hg (0.07, 0.05–0.08) and Zn (8.09, 4.41–11.36). The metal concentrations measured in the edible muscles of all fish species were found lower as compared to the contents in liver and gill. Analysis of variance revealed a significant difference in trace metal accumulation among the organs (p < 0.001), but the difference among the seasons and fish species was insignificant (p > 0.05), with the exception of Zn accumulation (p < 0.05). The estimated daily intake (EDI) of the trace metals through the consumption of fish as a dietary component varied widely from 0.48 to 21.33% with respect to the corresponding permissible tolerable daily intake (PTDI). The target hazard quotients (THQs) calculated considering these EDIs for individual metals indicated that the Cr and Cu metals dominantly contributed (avg. THQ = 0.198) to represent the hazard index (HI) than other metals (avg. THQ = 0.029). The average HI determined for all the species was <1 (0.484, ranged 0.255–0.605), indicating that these fish species of Chilika are safe for human consumption.