阳宗海沉积物中重金属生物有效性评估

通过测定和分析阳宗海表层沉积物中酸可挥发性硫化物(AVS)和同步提取重金属(SEM)的含量和分布特征,采用SEM/AVS方法对阳宗海表层沉积物中重金属的生物有效性进行评估;同时,采用生物有效阈值法评估了单一重金属的生物有效性。研究得出以下结论:阳宗海表层沉积物中AVS含量为15.09~149.74 μmol/g,平均值为49.42 μmol/g,从南向北呈递减趋势;AVS在南部和中部均与湖泊水深呈现正相关关系;∑SEM(包括Cu、Cr、Pb、Zn、Mn、As、Cd)含量分布波动较小,其范围为4.84~16.10 μmol/g,平均值为10.28 μmol/g,其分布规律为北部大于南部;阳宗海各采样点SEM/AVS<1,说明阳宗海表层沉积物中重金属不会对生物产生不良影响;从单一重金属来看,Pb可能经常产生生物毒性,Cu有可能产生生物毒性,其他金属除部分点可能产生生物毒性外,整体上几乎不会产生生物毒性。     

Vertical distribution of acid-volatile sulfide and simultaneously extracted metals in mangrove sediments from the Jiulong River Estuary,Fujian, China

Background Acid-volatile sulfide (AVS) is operationally defined as sulfides in sediment, which are soluble in cold acid, and is reported as the most active part of the total sulfur in aquatic sediments. It is a key partitioning phase controlling the activities of divalent cationic heavy metals in sediment. Methods In order to examine this in mangrove environments, six sites were selected along the Jiulong River Estuary in Fujian, China, which had previously been reported to be polluted by heavy metals. Sediments were sampled from 0–60 cm depth at each site, and the spatial distribution of AVS and SEM (simultaneously extracted metals: copper, cadmium, zinc, and lead) were determined. Results and Discussion The results indicate that the AVS concentrations had a spatial variation, ranging from 0.24 to 16.10 μmol g⁻¹ sediment dry weight. The AVS concentration in the surface layer is lower than that of the deeper sediment, with peak values in the 15–30 cm horizon. There was no correlation between the AVS value and organic matter content or total dissolved salts, but a significant positive correlation of AVS with surface sediment (0–5 cm) moisture content was found. This indicates that water logged sediments tend to have a high AVS value. The amount of SEM was within the range of 0.33–2.80 μmol g⁻¹ sediment dry weight and decreased with sediment depth. Conclusions There was a marked variation in AVS and SEM among different sites studied. AVS concentrations were generally lower in the surface sediments, while SEM concentrations slightly decreased with the depth. Higher concentrations of SEM found in the upper layers of the sediments confirm the earlier suggestions that this study area may suffer from increasing heavy metal pollution. Recommendations and Perspectives When monitoring environmental impacts by using AVS, the micro and large-scale spatial variation as well as vertical distribution need to be estimated to avoid misleading results. Both AVS and SEM concentrations in different sediment layers should be taken into account in assessing the potential impact of heavy metals on the biotic environment.     

Polycyclic Aromatic Hydrocarbon (PAH) Contamination of Surface Sediments from Port Dickson,Malaysia: Distribution,Sources and Ecological Risk Assessment

Distribution and sources of 16 parent polycyclic aromatic hydrocarbons (PAHs) were investigated in surface sediments from Port Dickson, Malaysia. Total PAHs varied from 481.3 to 976.6 with a mean value of 679.3 ng g^?1 dry weight, which can be classified as moderate level of pollution. The toxic assessment suggested that the PAHs in sediments will not cause immediately adverse biological effects. Both petrogenic and pyrogenic PAHs were recorded in the study area with dominance of pyrogenic. The authors believe that effective monitoring and implementation of environmental regulations have resulted in a tremendous improvement of sediment quality in the Malaysian aquatic ecosystem.     

The relation between Acid Volatile Sulfides (AVS) and metal accumulation in aquatic invertebrates: Implications of feeding behavior and ecology

The present study evaluates the relationship between Acid Volatile Sulfides (AVS) and metal accumulation in invertebrates with different feeding behavior and ecological preferences. Natural sediments, pore water and surface water, together with benthic and epibenthic invertebrates were sampled at 28 Flemish lowland rivers. Different metals as well as metal binding sediment characteristics including AVS were measured and multiple regression was used to study their relationship with accumulated metals in the invertebrates taxa.Bioaccumulation in the benthic taxa was primarily influenced by total metal concentrations in the sediment. Regarding the epibenthic taxa metal accumulation was mostly explained by the more bioavailable metal fractions in both the sediment and the water. AVS concentrations were generally better correlated with metal accumulation in the epibenthic invertebrates, rather than with the benthic taxa. Our results indicated that the relation between AVS and metal accumulation in aquatic invertebrates is highly dependent on feeding behavior and ecology.     

Spatio-Temporal Distribution of Polycyclic Aromatic Hydrocarbons (PAHs) in Atmospheric Air of Tamil Nadu,India, and Human Health Risk Assessment

This study analyzed the seasonal distribution and the possible sources of polycyclic aromatic hydrocarbons (PAHs) in the atmospheric environment of Tamil Nadu, India. Passive air sampling was performed at 32 locations during the period from April 2009 to January 2010, and PAHs were quantified using a gas chromatograph-mass spectrometer. Analysis showed that the concentrations of PAHs were in the range of 5–47.5 ng/m³ with uniform distribution in urban areas in all seasons. Pre-monsoon season showed the highest cumulative concentration of PAHs in both agricultural and coastal areas. Among PAHs, phenanthrene, fluoranthene, and pyrene levels were found to be predominant in all the samples, contributing up to 36%, 35.5%, and 24.5% of total PAHs, respectively. The signature of the PAHs obtained through diagnostic ratio and principal component analysis revealed that diesel emissions was the probable source of PAHs in all locations. Based on Word Health Organization guidelines, the human lung cancer risk due to observed level of PAH concentration (i.e., PAHs exposure) is meager. However, the risk is predicted to be more in the coastal area during summer (18 individuals among 0.1 million people). To the knowledge of these authors, this report is the first on the seasonal analysis of PAHs using passive air sampling in India.     

巢湖表层沉积物中重金属的分布特征及其污染评价

以巢湖表层沉积物为研究对象,利用BCR连续提取法研究了沉积物中Cr、Co、Ni、Cu、Cd、Zn、V和Pb等8种重金属元素的分布特征,同时运用潜在风险指数法和地累积指数法综合评价了巢湖沉积物中重金属的生态风险。结果表明,巢湖沉积物中的重金属含量在空间上表现出东西高、中间低的分布特征。巢湖表层沉积物中Cr、Co、Ni、V和Cu 5种重金属都主要以残渣态为主,Zn和Cd主要以弱酸提取态为主,Pb以可还原态为主,同时,Co和Cu 2种元素的可交换态及可还原态含量占有较高比例,具有潜在危害性。相关性分析显示,Cr、Cu、Pb、Ni、Zn和Cd 6种重金属元素的来源和分布可能具有相似性,Co和V 2种重金属元素具有相似的地球化学行为且其主要来源可能与其他几种重金属不同。潜在生态风险指数评价结果表明,巢湖表层沉积物中8种重金属元素构成的生态危害顺序为:Cd>Pb>Co>Cu>Ni>Zn>V>Cr,Cd具有高的生态危害等级,其他7种重金属元素均为低生态危害等级。地累积指数法评价结果表明:巢湖沉积物重金属元素的富集程度为Cd>Zn>Pb>Co>Cu>V>Ni>Cr,Cr属于清洁级别,Co、Cu、V和Ni处于轻度污染水平,Zn和Pb处于偏中度污染,Cd达到了重污染水平。     

Polychlorinated biphenyls (PCBs) in marine fishes from China: Levels, distribution and risk assessment

Muscle tissues of large yellow croakers (Pseudosciaena crocea) and sliver pomfret (Pampus argenteus) from nine coastal cities of East China including Dalian, Tianjin, Qingdao, Shanghai, Zhoushan, Wenzhou, Fuzhou, Quanzhou and Xiamen were analyzed for polychlorinated biphenyl (PCB) concentrations. Thirty-six PCB congeners were quantified in the fishes, of which 11 congeners were dioxin-like PCBs. The total PCB concentrations of the present study were at the low end of the global range, which may be related to the smaller usage and shorter consumption history of PCBs in China. PCBs 18, 29, 52, 66, 101, 104, 138, 153, 180 and 194 were the major constituents found in the fish samples. Regression analysis showed a strong positive correlation (R² = 0.800; p < 0.001) between total dioxin-like PCBs and total PCB concentrations, and that total PCB concentrations explain 80% of the variability in total dioxin-like PCB concentrations. Among the species investigated, significantly higher concentrations of total PCBs were found in croakers than in pomfrets, which may be attributed to their different feeding and living habits. No significant difference in total PCB concentrations among the cities was observed; principal component analysis (PCA) of PCB profiles indicated that PCB pollution came from similar sources in the sampling areas and that there may be other PCB sources in Dalian and Wenzhou. The calculated carcinogenic risks (CRs) from the two species based on a low consumption group and high consumption group were all greater than 10⁻⁶, suggesting that daily exposure to dioxin-like PCBs via fish consumption results in a lifetime cancer risk of greater than one in one million. In contrast, the hazard quotients (HQs) of noncancer risks were all less than unity.     

Triclosan in Fresh Water Fish Gibelion Catla from the Kaveri River,India, and Its Consumption Risk Assessment

Triclosan is a common antimicrobial agent that is found in significant levels in the aquatic environment and may elicit effects on aquatic organisms through unexpected modes of action. In this study, triclosan was quantified in fish from the Kaveri River, India, by using the gas chromatography and mass spectrometry technique and it was found in the range of 0.73–50 ng/g wet weight (ww). The mean bioaccumulation factor based on water (BAF_w 820) and sediment (BAF_s 2.12) in the Kaveri River showed that triclosan is accumulative in fish, and reflects its feeding behavior. The bioaccumulation indicates triclosan's persistence or prevalence throughout the river stretch. Human risk assessment through dietary intake demonstrated that the triclosan exposure is five orders of magnitude lower than the acceptable daily intake (50 μg/kg bw) and US EPA reference dose (300 μg/kg bw/day). This investigation is the first to report the bioaccumulation of triclosan in freshwater fish from India. Further, the results indicate that this fish acts as a biomarker of exposure for triclosan and thus shall be used to report triclosan pollution in the future.     

多孔陶瓷滤球对杭州西湖沉积物5种形态磷的吸附性能

以新型赤泥基多孔陶瓷滤球（porous ceramic filter material,PCFM）颗粒为吸附剂,采用动态和静态吸附实验相结合的实验方法研究了PCFM颗粒对沉积物磷的吸附性能。动态吸附实验结果表明,影响PCFM颗粒除磷效果的主要因素有投加量、反应时间、上覆水体pH值和环境温度,最佳吸附反应条件为PCFM投加量8 g,反应时间12 h,上覆水体pH=12,环境温度为50℃。静态吸附实验结果表明,随着反应时间的延长,PCFM对沉积物五种形态磷吸附在12 d左右接近或达到了吸附平衡,此时TP、OP、IP、Fe/Al-P和Ca-P的去除量分别为245.89、69.86、155.25、195.22和-49.01 mg·kg-1。可见PCFM对沉积物磷的吸附性能较好,可进一步应用于富营养化湖泊沉积物磷控制。     

安徽铜陵新桥河上游沉积物重金属污染及潜在生态风险评价

安徽铜陵新桥河的沉积物样中,重金属浓度为Cu〉Zn〉Pb〉Cr,按国家土壤环境二级质量标准评价,Cu、Zn含量已超标。其新桥河的沉积物样中,Cu、Zn的污染参数很高,含量为高风险或极高风险;Pb污染参数较高,含量为一般风险或高风险。同时新桥河的沉积物样中,Cu具有很高的潜在生态风险。     

多孔陶瓷滤球与沉水植物联合作用处理杭州西湖沉积物中的磷

首次将新型环保陶瓷滤球（red mud-based porous ceramic filter material,PCFM）作为吸附材料,与沉水植物处理沉积物磷技术相结合,通过测定沉积物各形态磷含量的变化,以期研究该吸附-生物联合修复技术对沉积物磷的修复效果。结果表明,苦草组对沉积物各形态磷去除量随时间的变化逐渐增大,苦草在150 d时对沉积物TP、IP、OP、Fe/Al-P和Ca-P的去除量分别为51.60、16.32、34.74、46.37和-14.99 mg·kg-1。研究不同PCFM厚度与沉水植物苦草联合对沉积物磷的去除效果,发现厚度5 cm PCFM+苦草对对沉积物各形态磷的去除效果最好。在150 d时,对沉积物TP、IP、OP、Fe/Al-P和Ca-P在的去除量分别达到652.61、249.12、396.40、314.38和72.11 mg·kg-1,苦草与陶瓷滤球在对沉积物磷的去除过程中,可能存在有益于去除沉积物磷的相互促进的作用。可见PCFM和苦草联合作用处理沉积物磷的效果较好,可进一步应用于富营养化湖泊沉积物磷控制工程。     

Halogenated organic contaminants (HOCs) in sediment from a highly eutrophicated lake, China: Occurrence, distribution and mass inventories

Halogenated organic contaminants (HOCs) including 16 polybrominated diphenyl ethers (PBDEs) and 37 polychlorinated biphenyls (PCBs) were determined in 49 surfacial sediments from Chaohu Lake, a highly eutrophicated lake, China. PBDEs were detected in almost samples with the range of the total concentration (defined as Σ₁₆PBDEs) from 0.84 to 86.6 ng g⁻¹. Compared with the occurrence of PBDEs in Pearl River Delta and Yangtze River Delta in China, lower percentage of BDE-209 over the concentration of Σ₁₆PBDEs was inferred by the high-volume application of penta-BDE mixture product for local domestic furniture purpose. The total concentration of 37 PCBs (Σ₃₇PCBs) ranged from 0.05 to 3.36 ng g⁻¹ with the most detection of PCB-1, -4, -52 and -71. Both the concentrations of Σ₁₆PBDE and Σ₃₇PCB poorly correlated with total organic carbon (TOC), suggesting the significant contribution of phytoplankton organic carbons to sediment TOC. The contamination by PBDEs and PCBs in western region of the lake was significantly more serious than in eastern lake. Our findings about the higher residues of PBDEs and PCBs in sediments at the estuary of Nanfei River compared to the other estuaries also supported the conclusion that urban area (Hefei city) was the main source of PBDEs and PCBs. The comparison with the concentration of HOC in the present study with those in other lacustrine sediments around the world suggested the contamination by PBDEs in Chaohu Lake is at middle of the global concentration range, whereas PCBs is at low end of the global range which could be elucidated by local economic development and historical usage of PBDEs and PCBs. The mass inventories of HOCs in the lake were estimated at 561 and 38 kg, which corresponds to only 0.000006% and 0.0001% of these global historical produce volumes, respectively.     

Vertical distribution and environmental significance of sulfur and oxygen heterocyclic aromatic hydrocarbons in soil samples collected from Beijing, China

Vertical distribution of the concentration and composition of some sulfur and oxygen heterocyclic aromatic hydrocarbons (SOHAHs), such as, fluorene, dibenzofuran, dibenzothiophene and their alkyl homologues in 10 soil profiles in Beijing have been investigated. The results showed that the concentrations and composition of SOHAHs in topsoil (0-30cm) from different profiles are different. The concentrations of SOHAHs in topsoils are much higher than that in bottom soils where the concentrations are relatively constant. The fingerprints of SOHAHs from same profile are similar in topsoil samples, which are obviously different at the deep part, which suggested that the sources of these compounds are consistent in topsoil and are discriminating between surface and bottom soils. The main sources of SOHAHs in surface soil were fossil fuel combustion, petroleum and wastewater irrigation, while those at deep part were likely derived from the degradation products of soil organic matters.     

Source Apportionment and Identification of Polycyclic Aromatic Hydrocarbons (PAHs) in Sediment Cores of Selected Creeks in Delta State,Nigeria

Polycyclic aromatic hydrocarbons (PAHs) seasonal variation and sources in Ubeji, Ifie, and Egbokodo Creeks of the Niger Delta, Nigeria, were predicted using diagnostic ratios (DRs) of parent PAHs (Phe/Phe + Ant; Flu/Flu + Pyr; BaA/BaA + Chry, and Ind/Ind + BghiP) and principal component analysis (PCA). A total of 222 sediment core samples were collected during the wet (August 2010) and the dry seasons (January 2011). The samples were dried and Soxhlet extracted; sample extracts were fractionated and analyzed by gas chromatography/flame ionization detection (GC/FID) to identify individual PAHs. The diagnostic PAH ratios revealed that PAHs in the sediment cores at the three creeks, in both seasons, mainly stemmed from the combustion process (pyrogenic sources). Principal component analysis further confirmed that wood-burning, coal combustion, diesel, gasoline-powered vehicular emissions, and petroleum combustion were the dominant contributors of PAHs sources at the sampling location. This study provided information on the origin and sources of PAHs in sediment cores, which may be useful for regulatory actions, environmental quality management, contamination history, and environmental forensic studies.     

水葫芦对滇池底泥氮磷营养盐释放的影响

为了探讨水葫芦对富营养湖泊底泥氮磷营养盐释放的影响,通过原位采集滇池柱状底泥,以蒸馏水为上覆水,进行了25d的室内静态模拟实验。实验比较了水葫芦处理组和空白对照组底泥氨氮（NH4-N）、硝态氮（NO3^-N）、溶解性总氮（DTN）、正磷酸盐（PO4^3--P）等的释放特征。结果表明,与对照组相比,水葫芦处理组上覆水溶解氧、pH显著性降低,而PO4^3-P浓度显著性升高;在实验前2d,水葫芦处理组上覆水NH4^＋N和DTN浓度显著性高于对照组,而在5～25d时,其显著性低于对照组。根据上覆水营养盐浓度、水葫芦植株吸收营养盐总量,推算底泥氮磷营养盐释放的平均速率,表明水葫芦加速了滇池底泥氮、磷营养盐的释放速率,处理组氮、磷释放速率分别为对照组的5．3～170．2和1．5～21．6倍。     

Methyl Tertiary Butyl Ether (MTBE) and Other Volatile Organic Compounds (VOCs) in Public Water Systems,Private Wells,and Ambient Groundwater Wells in New Jersey Compared to Regulatory and Human-Health Benchmarks

Potential threats to drinking water and water quality continue to be a major concern in many regions of the United States. New Jersey, in particular, has been at the forefront of assessing and managing potential contamination of its drinking water supplies from hazardous substances. The purpose of the current analysis is to provide an up-to-date evaluation of the occurrence and detected concentrations of methyl tertiary butyl ether (MTBE) and several other volatile organic compounds (VOCs) in public water systems, private wells, and ambient groundwater wells in New Jersey based on the best available data, and to put these results into context with federal and state regulatory and human-health benchmarks. Analyses are based on the following three databases that contain water quality monitoring data for New Jersey: Safe Drinking Water Information System (SDWIS), Private Well Testing Act (PWTA), and National Water Information System (NWIS). For public water systems served by groundwater in New Jersey, MTBE was detected at a concentration ≥10 μg/L, ≥20 μg/L, and ≥70 μg/L at least once in 30 (2%), 21 (1.4%), and five (0.3%) of sampled systems from 1997 to 2011, respectively. For private wells in New Jersey, MTBE was detected at a concentration ≥10 μg/L, ≥20 μg/L, and ≥70 μg/L at least once in 385 (0.5%), 183 (0.2%), and 46 (0.05%) of sampled wells from 2001 to 2011, respectively. For ambient groundwater wells in New Jersey, MTBE was detected at a concentration ≥10 μg/L, ≥20 μg/L, and ≥70 μg/L at least once in 14 (2.1%), 9 (1.3%), and 4 (0.6%) of sampled wells from 1993 to 2012, respectively. Average detected concentrations of MTBE, as well as detected concentrations at upper-end percentiles, were less than corresponding benchmarks for all three datasets. The available data show that MTBE is rarely detected in various source waters in New Jersey at a concentration that exceeds the State's health-based drinking water standard or other published benchmarks, and there is no evidence of an increasing trend in the detection frequency of MTBE. Other VOCs, such as tetrachloroethylene (PCE), trichloroethylene (TCE), and benzene, are detected more often above corresponding regulatory or human-health benchmarks due to their higher detected concentrations in water and/or greater toxicity values. The current analysis provides useful data for evaluating the nature and extent of historical and current contamination of water supplies in New Jersey and potential opportunities for public exposures and health risks due to MTBE and other VOCs on a statewide basis. Additional forensic or forecasting analyses are required to identify the sources or timing of releases of individual contaminants at specific locations or to predict potential future water contamination in New Jersey.     

河蚬对太湖梅梁湾沉积物中HCHs和DDTs的生物富集

以采自清洁水体的河蚬(Corbicula fluminea)为实验生物,利用生物富集实验测试了河蚬对太湖梅梁湾水源地沉积物中HCHs和DDTs的生物富集.研究结果表明,将河蚬暴露于有机氯农药污染程度相似的太湖梅梁湾沉积物中(HCHs和DDTs浓度分别为1.5-1.8.S/S(以干重计)和1.1-1.7 as/g(以干重计))后,随着暴露时间的延长(24～168h),河蚬对有机氯农药的富集量随着暴露时间逐渐增加.试验结束时各样点中河蚬对HCHs和DDTs的富集量分别为(9.4±2.2)ng/g(以干重计)、(20.7±7.6)ng/g(以干重计).实验水体沉积物中HCHs和DDTs的生物沉积物富集因子(BSAF)分别为1.5±0.1和4.4±0.7.生物-沉积物富集因子(BSAF)与有机物的辛醇-水比值(Kow)存在显著正相关.     

Spatial Distribution Patterns,Sources of Heavy Metals,and Relation to Ecological Risk of Surface Sediments of the Cyprus Northern Shelf (Eastern Mediterranean)

In this study, the spatial distribution of metals and the sources of metal pollution were investigated along the Northern Shelf of Cyprus (Mediterranean Sea). The concentrations of heavy metals and organic matter were measured in sediments collected from the Gemi Konagi, Girne, and Gazi Magusa areas. Measured metal values were compared with Mediterranean background concentrations. Cu and Zn concentrations at the Gemi Konagi area and all of the Cr values were higher than Mediterranean backgrounds. The metal levels were evaluated by the enrichment factor (EF), contamination factor (C_f) and degree of contamination (C_d). EF results indicated that heavy metal sources were probably originated from natural processes and mining activities. The C_f values of Hg indicated low contamination. The C_d (degree of contamination) values for all heavy metals also showed a low degree of contamination at the study area. Metal levels were also compared with the numerical Sediment Quality Guidelines (SQG) for an environmental risk assessment. Results showed that sediments were classified as heavily polluted by Cu and moderately polluted by Zn at Gemi Konagi and heavily polluted by Cr and Ni contamination at all sampling areas per the SQG.     

Polycyclic aromatic hydrocarbon (PAH) contamination of surface sediments and oysters from the inter-tidal areas of Dar es Salaam, Tanzania

Surface sediment and oyster samples from the inter-tidal areas of Dar es Salaam were analyzed for 23 polycyclic aromatic hydrocarbons (PAHs) including the 16 compounds prioritized by US-EPA using GC/MS. The total concentration of PAHs in the sediment ranged from 78 to 25,000 ng/g dry weight, while oyster concentrations ranged from 170 to 650 ng/g dry weight. Hazards due to sediment contamination were assessed using Equilibrium Partitioning Sediment Benchmarks and Threshold Effect Levels. Diagnostic indices and principle component analysis were used to identify possible sources. Interestingly, no correlation between sediment and oyster concentrations at the same sites was found. This is supported by completely different contamination patterns, suggesting different sources for both matrices. Hazard assessment revealed possible effects at six out of eight sites on the benthic communities and oyster populations. The contribution of PAH intake via oyster consumption to carcinogenic risks in humans seems to be low.