Assessment of heavy metal concentrations and associated resistant bacterial communities in bulk and rhizosphere soil of <Emphasis Type="Italic">Avicennia marina</Emphasis> of Pichavaram mangrove,India

Heavy metals are known to pose a potential threat to terrestrial and aquatic flora and fauna. Due to increasing human influence, heavy metal concentrations are rising in many mangrove ecosystems. Therefore, an assessment of heavy metal (Cd, Cr, Cu, Ni, Pb, Fe, Mn, and Zn) concentrations was conducted within the bulk soil and rhizosphere soil of Avicennia marina at the Pichavaram Mangrove Forest in India. The rhizosphere soil showed higher concentrations of metals than the bulk soil. Compared to the bulk soil, the metals Cd, Fe, Mn, and Zn were 6.0–16.7% higher, whereas Cr, Cu, Ni, and Pb were 1.7–2.8% higher concentration. Among the three selected sampling sites (dense mangrove forest, estuarine region, and sea region), the sea region had the highest concentration of all heavy metals except Zn. The trend of the mean metal concentration was Fe > Mn > Cr > Ni > Cu > Pb > Zn > Cd. Heavy metals concentrations elevated by the 2004 tsunami were persistent even after 4 years, due to sedimentary soil processes, the rhizosphere effect of mangroves, and anthropogenic deposition. Analysis of the heavy metal-resistant bacteria showed highest bacterial count for Cr-resistant bacteria and rhizosphere soil. The maximum level of heavy metal-resistant bacteria was observed at the site with the highest heavy metal contamination. The heavy metal-resistant bacteria can be used as indicator of heavy metal pollution and furthermore in bioremediation.     

Development of a two-stage washing and biodegradation system to remediate octachlorinated dibenzo-<Emphasis Type="Italic">p</Emphasis>-dioxin-contaminated soils

A two-stage system for octachlorinated dibenzo-p-dioxin (OCDD)-contaminated soil remediation was developed. Soil washing using emulsified oil (EO) was applied in the first stage for OCDD extraction followed by the second stage of bioremediation using P. mendocina NSYSU for remaining OCDD biodegradation. The major tasks included (1) determination of optimal soil washing conditions for OCDD extraction by EO, (2) evaluation of feasibility of OCDD biodegradation by P. mendocina NSYSU under aerobic cometabolic conditions using EO as the primary substrate, and (3) assessment of the effectiveness of OCDD removal using the two-stage system. During the soil washing stage, EO with two different oil-to-water ratios (1:50 and 1:200) and pore volumes were tested with initial soil OCDD concentration of 21,000 µg/kg. Results indicate that EO could effectively improve the solubility and desorption of OCDD in soils. Up to 74% of OCDD removal could be obtained after washing with 60 PVs of EO and dilution factor of 50. After the soil washing process, enriched P. mendocina NSYSU solution was added into the reactor to enhance the aerobic biodegradation of remaining OCDD in soils. P. mendocina NSYSU could use adsorbed EO globules as substrates and caused significant OCDD degradation via the aerobic cometabolic mechanism. Approximately 82% of the remaining OCDD could be removed after 50 days of operation, and P. mendocina NSYSU played important roles in OCDD biodegradation. Up to 87% of OCDD was removed through the EO washing and biodegradation process. The two-stage system is a potential technology to remediate dioxin-contaminated soils.     

Enzymatic degradation of polyhydroxyalkanoate using lipase from <Emphasis Type="Italic">Bacillus subtilis</Emphasis>

Polyhydroxyalkanoates (PHAs) are an important class of biodegradable polymers synthesized by a few bacteria under nutrient-limiting conditions. In this study, the lipase-catalysed degradation of PHA synthesized by Enterobacter sp. was monitored. For this, the lipase-encoding gene from Bacillus subtilis DI2 was PCR-amplified, cloned into a T vector system and sequenced. It was expressed in Escherichia coli DH5α cells, the recombinant enzyme was purified 24.25-fold, and its molecular weight was determined to be around 28 kDa. When PHA biodegradation studies were carried out with this enzyme, gel permeation chromatography showed 21.3 and 28.3 % molecular weight decrease and weight loss, respectively. Further, scanning electron micrographs revealed alterations in polymer surface morphology. Changes in molecular vibrations were noticed in the FTIR spectra. When the chemical shifts in NMR spectra were studied, a steep reduction in area under the peak at 1.57 ppm was observed. In the heating range of 30–930 °C employed during thermogravimetry analysis, the degraded sample showed a total of 45.82 % weight loss, as against 18.89 % for the native sample. The melting temperature (T _m) of the polymer was also brought down from 126.22 to 118.18 °C, as inferred from differential scanning calorimetry. Lipase-catalysed chain scission reactions could thus be used to generate low molecular weight functional biopolymers with wide-ranging pharmaceutical applications, such as in sustained drug release.     

Dynamics of diesel fuel degradation in contaminated soil using organic wastes

Bioremediation is an effective measure in dealing with such contamination, particularly those from petroleum hydrocarbon sources. The effect of soil amendments on diesel fuel degradation in soil was studied. Diesel fuel was introduced into the soil at the concentration of 5 % (w/w) and mixed with three different organic wastes tea leaf, soy cake, and potato skin, for a period of 3 months. Within 84 days, 35 % oil loss was recorded in the unamended polluted soil while 88, 81 and 75 % oil loss were recorded in the soil amended with soy cake, potato skin and tea leaf, respectively. Diesel fuel utilizing bacteria counts were significantly high in all organic wastes amended treatments, ranging from 111 × 106 to 152 × 106 colony forming unit/gram of soil, as compared to the unamended control soil which gave 31 × 106 CFU/g. The diesel fuel utilizing bacteria isolated from the oil-contaminated soil belongs to Bacillus licheniformis, Ochrobactrum tritici and Staphylococcus sp. Oil-polluted soil amended with soy cake recorded the highest oil biodegradation with a net loss of 53 %, as compared to the other treatments. Dehydrogenase enzyme activity, which was assessed by 2,3,5-triphenyltetrazolium chloride technique, correlated significantly with the total petroleum hydrocarbons degradation and accumulation of CO₂. First-order kinetic model revealed that soy cake was the best of the three organic wastes used, with biodegradation rate constant of 0.148 day^?1 and half life of 4.68 days. The results showed there is potential for soy cake, potato skin and tea leaf to enhance biodegradation of diesel in oil-contaminated soil.     

Efficiency assessment of aerobic biological effluent treatment plant treating pharmaceutical effluents

The present paper undertakes a study of the physico-chemical properties and toxic heavy metals content in the untreated and treated pharmaceutical effluents in order to evaluate the working efficiency of industrial effluent treatment plants. The treatment efficiency achieved for various parameters was conductivity (79.94%), alkalinity (93.91%), hardness (87.70%), chloride (89.24%), cyanide (79.66%), phosphate (99.19%), total dissolved solids (85.89%), total suspended solids (96.87%), salinity (52.41%), dissolved oxygen (27.32%), biochemical oxygen demand (83.39%) and chemical oxygen demand (72.21%). The removal efficiency achieved for different heavy metals was Cu²⁺ (79.66%), Ni²⁺ (69.22%), Cr⁶⁺ (80.15%), Pb²⁺ (72.14%), Fe³⁺ (92.59%) and Zn²⁺ (90.61%). The level of biochemical oxygen demand (64 mg L^?1) in the treated effluents was above the limit of 30.0 mg L^?1, chemical oxygen demand level (208 mg L^?1) was close to a limit of 250 mg L^?1, while average Pb²⁺ concentration (0.10 mg L^?1) was on the borderline of maximum permissible limit of 0.10 mg L^?1 set by Central Pollution Control Board for safe discharge of industrial effluent in inland surface water. The average concentration of cyanide (0.01 mg L^?1) in the treated industrial effluent of our study is of great concern to the fisheries of freshwater ecosystem in which the effluents finally get discharged. Based on the results of the present study, it is concluded that the pollution level in the discharged pharmaceutical effluent is of the great concern requiring proper treatment and regular scientific monitoring so as to protect the environmental degradation of water resources and facilitate the propagation of the aquatic life.     

Biodegradation of phenol from a synthetic aqueous system using acclimatized activated sludge

Phenol is one of the aromatic hydrocarbons. Phenol and its derivatives are highly toxic. These pollutants can be observed in the effluents of many industries. This research investigates the removal of phenol by the use of activated sludge in a batch system. The effects of influencing factors on biodegradation efficiency have been evaluated. The main factors considered in this study were the volume of acclimatized activated sludge inoculation, pH, temperature, and initial concentration of phenol. The inoculation volumes of 1, 3, and 5 mL of acclimatized activated sludge were taken into account. Different pH values of 3, 5, 7, 9, and 11 were examined. The experiments were conducted for temperatures of 25, 30, 35, and 40 °C and initial phenol concentrations of 400, 800, 1,000, and 1,500 ppm. The results show that the acclimatized activated sludge has a high capacity for the removal of phenol. From a 100-mL aqueous solution was removed 1,500 ppm of phenol after 80 h. Furthermore, maximum phenol removal was observed for an inoculation volume of 5 mL for three different phenol concentrations of 100, 400, and 800 ppm. The best pH was 7 for the biodegradation process, and the optimum temperature was 30 °C. It was further found that an increase in the phenol concentration increased its removal time. Moreover, the activated sludge could effectively remove about 99.9 % of phenol from a synthetic aqueous solution in a batch system.     

Microbiological degradation of phenol using two co-aggregating bacterial strains

Phenol biodegradation in an aerobic batch reactor was investigated using mixed two co-aggregating strains (Flavobacterium sp. and Acetobacter sp.). Response surface methodology by the Box–Behnken model was used to evaluate the optimal cell growth and phenol degradation conditions. The optimum temperature, pH value and inoculum size were found to be 33 °C, 6.06 and 13 %, respectively. In the conditions, phenol degradation rate and biomass were predicted to be 96.97 % and 410.78 mg/L within the range examined, respectively. Less toxic acetaldehyde, ethanol and acetic ether were identified as main intermediate products from the degraded samples using GC–MS. Substrate inhibition was calculated from experimental biomass growth and phenol degradation parameters using the Haldane equation. Kinetic parameters derived from nonlinear regression with correlation factors (R ²) were 0.9682 for phenol degradation and 0.9594 for biomass growth, respectively. The phenol concentration to avoid substrate inhibition was 278.17 mg/L.     

Geochemical study of different-aged mining dump materials in the Freiberg mining district, Germany

Historical mining dumps are useful archives for the investigation of weathering processes. The objective of this study was to investigate the weathering behavior of waste-rock material derived from the 800-year-old silver ore mining in Freiberg, Germany. For identifying time-dependent weathering indices, dumped material of four dumps of different ages and corresponding rock was examined regarding the geochemical composition. The dumped material is characterized by high contents of heavy metal containing sulfidic ores, such as pyrite, arsenopyrite, sphalerite and galena. Acid mine drainage is produced by the oxidative weathering of the sulfide minerals and causes the increased dissolving of soluble metals with increasing age of dumps. As a result of these weathering processes, a clear depletion of chalcophile elements in the older dump material (800 years) compared to the youngest dump (100 years) was observed. In the soil horizons downstream the dumps, high quantities of heavy metals (e.g., up to 12,000 ppm As, 3,300 ppm Pb, 640 ppm Zn), mainly adsorbed on organic matter, were determined and indicate a time-dependent element transfer from the dumps into their surrounding soils.     

Adsorption of copper and zinc onto natural clay in single and binary systems

Calcareous and smectitic clay samples from the Coniacian–Lower Campanian system, Tunisia, were used as adsorbents for the removal of copper and zinc from aqueous solutions in single and binary systems. Calcareous clay sample was treated with acetic acid to obtain carbonate-free sample that was also used for metals removal. The adsorption of metal ions onto natural clay was tested in a batch method by mixing 1 g/L of each sample with a metal ion solution of zinc (300 μmol/L) and/or copper 600 μmol/L under the operating pH of 6, and agitation speed of 200 rpm within the equilibrium time of 60 min at 25 °C for single and binary systems. Our results showed that natural clay samples were mainly composed of silica, alumina, iron, and magnesium oxides. Adsorption data showed that the studied clay samples removed substantial amounts of heavy metals in single and mixed systems. Initial solution pH and carbonates contents enhanced the removal capacities of the studied clay samples, confirming their strong influencing effects. Thermodynamic parameters indicated an endothermic adsorption for metals removal by calcareous clay, but exothermic process for the smectitic sample. These results suggest that the Late Cretaceous clays, Tunisia, can be effectively used as natural adsorbents for the removal of toxic heavy metals in aqueous systems.     

Evaluation of <Emphasis Type="Italic">smtA</Emphasis> expression and <Emphasis Type="Italic">E. coli</Emphasis> survival against cadmium ions

Cadmium and other heavy metals lead to environmental danger, and these heavy metals are a great threat to human and other animal’s health. Investigation of the relationship between survival of E. coli and metallothionein smtA gene expression against cadmium ion is the goal of this research. Survival of recombinant bacteria containing smtA gene was analyzed against various concentrations of cadmium chloride salt using optical density (OD). At the resistive range, recombinant bacteria were subjected to different treatments. At the logarithmic phase of bacterial growth, sampling, RNA extraction and cDNA synthesis were performed and smtA gene expression was then analyzed by real-time PCR using designed primers for smtA gene and Amp resistance (as the calibrator gene). Relative gene expression was calculated using the ??C_t method. The resistive range against cadmium chloride was 0.5–0.7 mM (minimum inhibitory concentration (MIC = 0.5 mM)). Survival and gene expression analysis showed that in induced bacteria, smtA expression was increased significantly that in turn conferred resistance to cadmium chloride prominently. There was a direct relationship between increased smtA gene expression and survival of the recombinant bacteria. Therefore, our result may help to confront to cadmium metal environmental pollution using overexpression of smtA gene expression in recombinant bacteria.     

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.     

Competitive interference during the biodegradation of cresols

Phenol and its methylated derivatives, cresol isomers, are hazardous pollutants that are commonly present in various industrial effluents and known to have detrimental effect on aquatic life as well as human health, due to their toxic and carcinogenic nature. It is essential, therefore, to reduce the concentration of these contaminants in industrial effluent to acceptable levels prior to being discharged into the environment. Bacterial cells of the strain Pseudomonas putida, with excellent biodegradation capabilities and high tolerance of cresols, were extracted and immobilized in polyvinyl alcohol (PVA) gel for cresols biodegradation. The biodegradation was carried out at different operating conditions, in both batch and continuous modes, using a cylindrical spouted bed bioreactor. Factors affecting o-cresol and m-cresol degradation were studied in batch experiments, and the results showed that the immobilized bacteria could tolerate cresols concentration up to 200 mg/l. Moreover, the experiments indicated that the biodegradation rate was highly affected by the operating parameters such as pH and temperature, with optimum ranges of 6–8 for pH and 30–35 °C for temperature. However, the optimum conditions were different for each cresol isomer. The potential of P. putida in degrading binary and ternary mixtures of cresols was also examined in the continuous process and compared with single component biodegradation. The experimental results revealed that the biodegradation of o-cresol was highly inhibited by the presence of p-cresol and m-cresol.     

Microbial decolorization and degradation of crystal violet dye by <Emphasis Type="Italic">Aspergillus niger</Emphasis>

Two fungi were isolated and examined to decolorize crystal violet dye, frequently used as textile dye and in microorganism staining, using basal salt medium under static condition at 30 °C. The more effective fungus gave less dry weight and lower pH indicating that the process was directed toward the decolorization process giving acidic products rather than microbial growth. The effective fungus was identified as Aspergillus niger and was used in the rest of experiments. Increasing the incubation period more than 10 days did not improve the decolorization process, while the best pH was 5.5. The decolorization process was effective (up to 84.6 %) with the examined range of dye concentrations (10–40 ppm). Sucrose content, as a carbon source, more than 1 % did not improve the decolorization process (80.9 %). Using ammonium sulfate as a nitrogen source, instead of sodium nitrate in the original basal medium, lowered the decolorization process, while using corn steep liquor enhanced the biodegradation up to 96.1 %. Although the dye violet color vanishes in acid medium because of decreasing the possibility of extending the benzene chromophore as a result of binding the nitrogen lone pair in the ammonium ion, the UV–Vis spectra and LC–MS–ESI analysis of the bioassay products proved that the decolorization is due to the biodegradation of the dye rather than the resonance factor in acidic medium or biosorption by fungus mycelia.     

Degradation Kinetics of Petroleum Contaminants in Soft-Water Systems

On the basis of site investigation and sample collection of petroleum contaminants in the soil-water-crop system in the Shenyang-Fushun sewage irrigation area, the physical-chemical-biological compositions of the unsaturated zone is analyzed systematically in this paper. At the same time, the degradation kinetics of residual and aqueous oils is determined through biodegradation tests. The studies show that dominant microorganisms have been formed in the soils after long-term sewage irrigation. The microorganisms mainly include bacteria, and a few of fungus and actinomycetes.After a 110-days‘ biodegradation test, the degradation rate of residual oil is 9.74%--10.63%, while the degradation rate of aqueous oil reaches 62.43 %. This indicates that the degradation rate of low-carbon aqueous oil is higher than that of highcarbon residual oil. In addition, although microbial degradation of petroleum contaminants in soils is suitable to the firstorder kinetics equation, the half-lives of aqueous oil, No. 20 heavy diesel and residual oil in the surface soils (L2-1, S1-1 and X1-1) are 1732 h, 3465 h and 17325 h, respectively.     

Degradation of digested sewage sludge residue under anaerobic conditions for mine tailings remediation

Previous studies showed that 85 % of total organic matter (TOM) in digested sewage sludge (biosolids) used as a sealing layer material over sulfide tailings at the Kristineberg Mine, northern Sweden, had been degraded 8 years after application, resulting in a TOM reduction from 78 to 14 %. To achieve a better understanding of the field observations, laboratory studies were performed to evaluate biodegradation rates of the TOM under anaerobic conditions. Results reveal that the original biosolid consisted of ca. 60 % TOM (48.0 % lignin and 11.8 % carbohydrates) that had not been fully degraded. The incubation experiments proved that 27.8 % TOM in the biosolid was further degraded anaerobically at 20–22 °C during the 230 days’ incubation period, and that a plateau to the biodegradation rate was approached. Based on model results, the degradation constant was found to be 0.0125 (day^?1). The calculated theoretical gas formation potential was ca. 50 % higher than the modeled results based on the average degradation rate. Cumulated H₂S equated to 0.65 μmoL g^?1 of biosolid at 230 days. However, the large sulfurous compounds reservoir (1.76 g SO₄ ^2? kg^?1 biosolid) together with anaerobic conditions can generate high concentrations of this gas over a long-term perspective. Due to the rate of biodegradability identified via anaerobic processes, the function of the biosolid to serve as an effective barrier to inhibit oxygen migration to underlying tailings, may decrease over time. However, a lack of readily degradable organic fractions in the biosolid and a large fraction of organic matter that was recalcitrant to degradation suggest a longer degradation duration, which would prolong the biosolid material’s function and integrity.     

Isolation of <Emphasis Type="Italic">Bacillus cereus</Emphasis> from botanical soil and subsequent biodegradation of waste engine oil

Waste engine oil causes a vital environmental pollution when it spill during change and transportation and products of waste engine oil causes lethal effects to the living systems. Thus, abiotic and biotic approaches are being extensively used for removal of waste engine oil pollution. Therefore in present study, waste engine oil degradation was accomplished by a new bacterial culture, isolated from the soil by an enrichment technique. Morphological, biochemical and gene sequence analysis revealed that isolate was Bacillus cereus. Subsequently, biodegradation potential of B. cereus for waste engine oil was studied. Experimental variables, such as pH, substrate concentration, inoculum size, temperature and time on the biodegradation, were checked in mineral salt medium. The biodegradation efficiency of B. cereus was determined by gravimetry, UV–visible spectrophotometry and gas chromatography. In addition, waste engine oil was also characterized by GC–MS and FTIR for its major constituents, which showed total 38 components in waste engine oil, including hopanes, benzopyrene, long-chain aliphatic hydrocarbons, dibenzothiophenes, biphenyl and their derivatives. Results of successive biodegradation indicated that B. cereus was capable to degrade 1% of waste engine oil with 98.6% degradation potential at pH 7 within 20 days. Hence, B. cereus presents an innovative tool for removing the engine oil from the contaminated area.     

Improvement of cadmium ion electrochemical removal from dilute aqueous solutions by application of multi-stage electrolysis

Improvement of cadmium ion electrochemical removal from dilute aqueous solutions in a spouted bed reactor was investigated. Enlargement of cathode surface area from 1,000 to 1,500 cm² resulted in a decrease of nearly 30 % in both of the process time and the specific energy consumption. Application of a three-stage electrolysis process for a solution containing initial concentration of 270 ppm cadmium ion, resulted in the removal of 99.9 % cadmium ion in 135 min with the specific energy consumption of 2.29 kWh/kg, 23 % less than the value of a single-stage process. For a solution with cadmium ion initial concentration of 180 ppm, 99.9 % of cadmium ion was removed in 135.5 min by application of a two-stage electrolysis process, while the specific energy consumption was 2.82 kWh/kg, 30 % less than that of a single-stage process. For a solution with cadmium ion initial concentration of 90 ppm, 99.5 % of cadmium ion was removed in 100.2 min with the specific energy consumption of 3.78 kWh/kg in a single-stage electrolysis process.     

On the geological availability of germanium

Based on a detailed statistical analysis of chemical data published in the scientific literature, estimates were made of the minimum amounts of recoverable Ge contained within sulphidic zinc ores and coals, given current processing technologies. It is expected that at least 119 kt (～7 kt in zinc ores and ～112 kt in coal) of recoverable germanium exist within proven reserves (at present stage of knowledge) at grades in excess of 100 ppm in sphalerite and 200 ppm in coal, while at least 440 kt (～50 kt in zinc ores and ～390 kt in coal) should become recoverable in the future, being associated to coal reserves at 8–200 ppm Ge and zinc resources containing in excess of 100 ppm Ge in sphalerite. Mississippi Valley Type (MVT) deposits are expected to be the most important hosts of germanium-rich sphalerite, while both brown and hard coals are expected to be equally important as hosts of germanium. The approach taken in this publication shows that reliable minimum estimates for the availability of by-product metals lacking suitable reserve/resource data may be attained by using robust statistical methods and geochemical data published in the scientific literature     

Degradation of carbon disulphide (CS2) in soils and groundwater from a CS2-contaminated site

This study is the first investigation of biodegradation of carbon disulphide (CS₂) in soil that provides estimates of degradation rates and identifies intermediate degradation products and carbon isotope signatures of degradation. Microcosm studies were undertaken under anaerobic conditions using soil and groundwater recovered from CS₂-contaminated sites. Proposed degradation mechanisms were validated using equilibrium speciation modelling of concentrations and carbon isotope ratios. A first-order degradation rate constant of 1.25 × 10^?2 h^?1 was obtained for biological degradation with soil. Carbonyl sulphide (COS) and hydrogen sulphide (H₂S) were found to be intermediates of degradation, but did not accumulate in vials. A ¹³C/¹²C enrichment factor of ?7.5 ± 0.8 ‰ was obtained for degradation within microcosms with both soil and groundwater whereas a ¹³C/¹²C enrichment factor of ?23.0 ± 2.1 ‰ was obtained for degradation with site groundwater alone. It can be concluded that biological degradation of both CS₂-contaminated soil and groundwater is likely to occur in the field suggesting that natural attenuation may be an appropriate remedial tool at some sites. The presence of biodegradation by-products including COS and H₂S indicates that biodegradation of CS₂ is occurring and stable carbon isotopes are a promising tool to quantify CS₂ degradation.     

Response of sediment-dwelling annelida community in relation to geochemical parameters in the Gorgan Bay,Caspian Sea

This study aimed to investigate the population of annelida communities in relation to environmental factors and heavy metals accumulated in sediments of the Gorgan Bay. The pollution load index and potential ecological risk (PER) were calculated. The results indicated mean concentrations (ppm) of heavy metals were (mean ± SD) Pb: 11.5 ± 4.88, Cu: 18 ± 8.83, Zn: 42 ± 22.15, Ni: 29.20 ± 14.68, Co: 10.56 ± 14.68, As: 7.77 ± 2.12, Sr: 1,449 ± 902.59 and V: 26.64 ± 10.25. Considering PER, sediments of the Gorgan Bay had low ecological risk. Based on abundance data, dominant species were Streblospio gynobranchiata, Nereis diversicolor, Tubificoides fraseri and Tubificidae unknown, respectively. Results of redundancy analysis displayed that T. fraseri and N. diversicolor were associated with high values of Sr. All the species were negatively correlated with As. There were positive correlation between S. gynobranchiata and N. diversicolor with values of clay, salinity, depth and silt. The present study provided the relative importance of heavy metals and environmental variables which partly assist in structuring assemblages of annelida in a transitional area.