SEMIPERMEABLE MEMBRANE DEVICES USED TO ESTIMATE BIOCONCENTRATION OF POLYCHLORINATED BIPHENYLS1

ABSTRACT: Aquatic organisms passively accumulate hydrophobic organic compounds, such as polychlorinated biphenyls, even when ambient water concentrations of the contaminant are below analytical detection limits. However, contaminant concentrations in tissue samples are subject to an inherently high level of variability due to differences in species, life stage, and gender bioconcentration potentials. Semipermeable membrane devices (SPMDs) were used to sample Aroclor 1254, a mixture of readily bioconcentrated polychlorinated biphenyls (PCBs), in a contaminated wetland near Flat Top, WV. The devices consisted of triolein, a lipid found in fish, enclosed in a polyethylene membrane. SPMDs were deployed in the water column and in direct contact with wetland sediments along a previously identified concentration gradient of PCBs. The devices were retrieved after a 25-day exposure period. Analytes were recovered by dialyzing the devices in nanograde hexane. Hexane dialysates were condensed and analyzed by gas chromatography. All deployed devices sequestered quantifiable amounts of Aroclor 1254. Water-column SPMDs accumulated PCBs far in excess of ambient water concentrations. The devices contacting sediments accumulated PCBs at all sites, though accumulated concentrations did not exceed concentrations in sediment. Patterns of PCB concentration in the devices corresponded to the identified gradient at the site. Results from the water-column SPMDs were used to estimate the concentration of the dissolved, bioavailable fraction of PCBs present in the water column. These concentrations ranged from 0.01 to 0.09 μg/L of bioavailable Aroclor 1254.     

气相色谱-质谱法测定地表水体中多氯联苯

建立以液液萃取-气相色谱质谱法测定地表水中7种Aroclors(Aroclor1016、Aroclor1221、Aroclor1232、Aroclor1242、Aroclor1248、Aroclor1254、Aroclor1260)的方法。通过对7种Aroclors色谱图分析,确定7种Aroclors定量峰,共计22种多氯联苯单体。采用Aroclor标准溶液进行校准曲线、方法检出限、准确度及精密度分析。实验结果显示,线性关系良好,相关系数均在0.995以上,检出限范围为0.001～0.003 g/L,对0.20 g/L的水样进行回收率及精密度测定,加标回收率为81.2%～112%,相对标准偏差(RSD)为7.1%～13.8%。     

Activated carbon immobilizes residual polychlorinated biphenyls in weathered contaminated soil

Activated carbon (AC) has recently been shown to be effective in sequestering persistent organic pollutants (POPs) from aquatic sediments. Most studies have demonstrated significant reductions of POP concentrations in water and in aquatic organisms; however, limited data exist on the possibility of using AC to immobilize remaining POPs at terrestrial contaminated sites. Under greenhouse conditions, pumpkin ssp cv. Howden) were grown, and red wiggler worms () were exposed to an industrial contaminated soil containing a mixture of polychlorinated biphenyls (PCBs), i.e., Aroclors 1254 and 1260) treated with one of four concentrations of AC (0.2, 0.8, 3.1, and 12.5%) for 2 mo. The addition of AC to contaminated soils virtually eliminated the bioavailability of PCBs to the plant and invertebrate species. There were reductions in PCB concentrations of more than 67% in ssp and 95% in . These data suggest that AC could be included as part of comprehensive site closure strategy at PCB-contaminated sites.     

Sources and Distribution of Polychlorinated Terphenyls at a Major US Aeronautics Research Facility

O -deethylase (EROD) activity to a similar degree as PCB Aroclor 1254 and to a greater extent than PCT Aroclor 5460. The presence of high concentrations of PCTs contributed to the facility being included on the National Priorities List. It subsequently became the first US federal facility to sign a Federal Facility Agreement, identifying cleanup responsibilities, prior to formal listing.     

Phytoremediation of polychlorinated biphenyl (PCB)-contaminated sediment: a greenhouse feasibility study

Contaminated sediments dredged from navigable waterways often are placed in confined disposal facilities to prevent further spread of the pollutants. Reducing contaminants to acceptable levels would allow for disposal of the sediments and further dredging activity. A greenhouse study was conducted to evaluate plant treatments and the addition of an organic amendment to decrease the concentration of PCB congeners found in Arochlor 1260. Sediment treated with the amendment and either low transpiring plants or no plants had the greatest removal of the PCB congeners. High-transpiring plants apparently prevented the highly reducing conditions required for reductive dechlorination of highly chlorinated PCBs. Most likely, the amendment provided labile carbon that initiated the reducing conditions needed for dechlorination. The sediment moisture content and moisture-related plant parameters were significant predictors of the PCB loss. Carex aquatalis and Spartina pectinata are predicted to be the most effective plant treatments for phytoremediation of PCBs.     

Chemical Characteristics of Urban Stormwater Sediments and Implications for Environmental Management, Maricopa County, Arizona

On the basis of published guidelines, urban stormwater sediments do not appear to constitute a major regional environmental problem with respect to the chemical characteristics investigated here. At individual sites, high concentrations of organic compounds—chlordane, dieldrin, PCBs, and toxaphene—may require some attention. The possible environmental hazard presented by low-level organochlorine contamination is not addressed in this paper; however, high levels of toxicity in urban sediments are difficult to explain. Sediment toxicity varied significantly with time, which indicates that these tests should be evaluated carefully before they are used for management decisions.     

Development and use of site-specific chemical and biological criteria for assessing New Bedford Harbor pilot dredging project

Numerical site-specific chemical and biological criteria were established to assess the impact of a pilot dredging project on water quality at the New Bedford Harbor, Massachusetts, USA, Superfund site. Because most existing chemical concentrations in the water column and indigenous biota exceeded federal and state water quality limits, the derivation of site-specific criteria was required. Prior to any operational phases of the project (i.e., dike construction, dredging), criteria values were developed from background concentrations of PCBs and metals in water and biota, as well as for the toxic effects of water quality on the biota. During each operational phase of the project, water samples were collected, analyzed within 16 h, and the data supplied to a management committee in order to assess the environmental impact of the previous days' operation. The ambient unfiltered water concentration of PCBs and metals were the only chemical or biological criteria exceeded. Modification of the next days' operations resulted in a return of these concentrations to background levels. The combined use of site-specific criteria and a real-time decision making management process allowed for successful completion of this project with a minimal effect on water quality.     

Spatial and temporal distribution of polychlorinated biphenyl (PCB) concentrations in soils of an industrialized city in Turkey

Surface soil (0-5 cm) samples from 43 sampling sites covering the entire urban territory of Bursa, an industrialized city in Turkey, were collected in each season and analyzed for 83 polychlorinated biphenyls (PCBs). The mean concentration of total PCBs (Σ83 PCBs) among all sites over the four seasons was 2121.51 pg/g dry weight (dw), with a range of 207.61-5461.95 pg/g dw. Total PCB concentrations in the soil samples collected near an industrial region were the highest in all seasons. In general, PCB patterns were dominated by low-chlorinated homologue groups (≤ 5 Cl groups at a 79% level). The predominant homologue group found in Bursa city soils was the penta-CBs (29.1%) followed by the tetra-CBs (25.5%) and tri-CBs (17.6%). A total of seven dioxin-like PCB congeners (CB-77, 81, 105, 114, 118, 123, and 126) were found in every sampling location and their mean total concentration for all locations and seasons was 259.27 pg/g dw, with a range of 7.02-1581.13 pg/g dw. A significant relationship (r = 0.77, p < 0.01) was found between the concentrations of dioxin-like PCBs and the seasonal average sum of PCB concentrations. A correlation between light congeners (相似文献   

Aquatic organotin pollution in Taiwan

The current status of aquatic organotin pollution in Taiwan is reviewed. In freshwater sediments and biota, especially in rice-field related habitats, phenyltins (PTs) were dominant among the organotin pollutants, whereas butyltins (BTs) were usually predominant in marine environments. Among the marine habitats, contamination levels were found to be in the descending order of harbour and estuary>fish cultural site>coastal>offshore>coral reefs. Imposex snails were observed in all the sampling years (1990-2003). Meanwhile, organotin concentrations were greater in winter than those in summer, whereas proportions of PTs were much higher in summer than in winter. Due to the lack of continuous monitoring data, the effectiveness of the ban on TPT usage in agriculture in 1999 and the prohibition of TBT use on small boats in 2003 is still not known.     

Pleasure Boatyard Soils are Often Highly Contaminated

The contamination in pleasure boatyards has been investigated. Measured concentrations of copper, zinc, lead, mercury, cadmium, tributyltin (TBT), the 16 most common polycyclic aromatic hydrocarbons (∑16 PAHs), and the seven most common polychlorinated biphenyls (∑7 PCBs) from investigations at 34 boatyards along the Swedish coast have been compiled. The maximum concentrations were 7,700 for Cu, 10,200, for Zn, 40,100 for Pb, 188 for Hg, 18 for Cd, 107 for TBT, 630 for carcinogenic PAHs, 1,480 for ∑16 PAHs, and 3.8 mg/kg DW for ∑7 PCB; all 10–2,000 higher than the Swedish environmental qualitative guidelines. In addition, the mean of the median values found at the 34 places shows that the lower guidance value for sensitive use of land was exceeded for the ∑7 PCBs, carcinogenic PAHs, TBT, Pb, Hg, and Cu by a factor of 380, 6.8, 3.6, 2.9, 2.2 and 1.7, respectively. The even higher guideline value for industrial use was exceeded for the ∑7 PCBs and TBT by a factor of 15 and 1.8, respectively. TBT, PAHs, Pb, Cd, and Hg are prioritized substances in the European Water Framework Directive and should be phased out as quickly as possible. Because of the risk of leakage from boatyards, precautions should be taken. The high concentrations measured are considered to be dangerous for the environment and human health and highlight the urgent need for developing and enforcing pleasure boat maintenance guidelines to minimize further soil and nearby water contamination.     

Temporal and spatial distributions of sediment total organic carbon in an estuary river

Understanding temporal and spatial distributions of naturally occurring total organic carbon (TOC) in sediments is critical because TOC is an important feature of surface water quality. This study investigated temporal and spatial distributions of sediment TOC and its relationships to sediment contaminants in the Cedar and Ortega Rivers, Florida, USA, using three-dimensional kriging analysis and field measurement. Analysis of field data showed that large temporal changes in sediment TOC concentrations occurred in the rivers, which reflected changes in the characteristics and magnitude of inputs into the rivers during approximately the last 100 yr. The average concentration of TOC in sediments from the Cedar and Ortega Rivers was 12.7% with a maximum of 22.6% and a minimum of 2.3%. In general, more TOC accumulated at the upper 1.0 m of the sediment in the southern part of the Ortega River although the TOC sedimentation varied with locations and depths. In contrast, high concentrations of sediment contaminants, that is, total polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs), were found in sediments from the Cedar River. There was no correlation between TOC and PAHs or PCBs in these river sediments. This finding is in contradiction to some other studies which reported that the sorption of hydrocarbons is highly related to the organic matter content of sediments. This discrepancy occurred because of the differences in TOC and hydrocarbon source input locations. It was found that more TOC loaded into the southern part of the Ortega River, while almost all of the hydrocarbons entered into the Cedar River. This study suggested that the locations of their input sources as well as the land use patterns should also be considered when relating hydrocarbons to sediment TOC.     

Forest fertilization with wood ash: effect on the distribution and storage of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs)

Before wood ash can be safely used as a fertilizer in forests, possible negative effects such as input of organic contaminants or remobilization of contaminants already stored in the soil must be investigated. The objective of this study was to examine the effects of wood ash application on concentrations, storage, and distribution of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) in a Swiss forest soil. In May 1998, we added 8 Mg wood ash ha(-1) to a forest soil. We determined 20 PAHs and 14 PCBs in the organic layer, in the bulk mineral soil, and in soil material taken from preferential flow paths and from the matrix before and after the wood ash application. In the control plots, the concentrations of PAHs in the organic layer indicated moderate pollution (sum of 20 PAHs: 0.8-1.6 mg kg(-1)), but sum of PCB concentrations was high (21-48 microLg kg(-1)). The wood ash had high concentrations of PAHs (sum of 20 PAHs: 16.8 mg kg(-1)), but low concentrations of PCBs (sum of 14 PCBs: 3.4 microg kg(-1)). The wood ash application increased the PAH concentrations in the organic horizons up to sixfold. In contrast, PCB concentrations did not change in the Oa horizon and decreased up to one third in the Oi and Oe horizons. The decrease was probably caused by the mobilization of stored PCBs because of the high pH of the wood ash. This probably results in a higher mobility of dissolved organic matter, acting as PCB carrier. In the mineral soil, the preferential flow paths of the A horizon contained more PAHs and PCBs (+20 +/- 15% and +43 +/- 60%, respectively) than the matrix. This was particularly true for higher molecular weight compounds (molecular weight > 200 g mol(-1)). Below 50 cm depth, concentrations of PAHs and PCBs were smaller in the preferential flow paths, suggesting that in deeper depths, processes acting as sinks dominated over inputs in the preferential flow paths.     

Streamside Forest Buffer Width Needed to Protect Stream Water Quality,Habitat, and Organisms: A Literature Review

This literature review addresses how wide a streamside forest buffer needs to be to protect water quality, habitat, and biota for small streams (≤~100 km² or ~5th order watershed) with a focus on eight functions: (1) subsurface nitrate removal varied inversely with subsurface water flux and for sites with water flux >50 l/m/day (~40% avg base flow to Chesapeake Bay) median removal efficiency was 55% (26‐64%) for buffers <40 m wide and 89% (27‐99%) for buffers >40 m wide; (2) sediment trapping was ~65 and ~85% for a 10‐ and 30‐m buffer, respectively, based on streamside field or experimentally loaded sites; (3) stream channel width was significantly wider when bordered by ~25‐m buffer (relative to no forest) with no additional widening for buffers ≥25 m; (4) channel meandering and bank erosion were lower in forest but more studies are needed to determine the effect of buffer width; (5) temperature remained within 2°C of levels in a fully forested watershed with a buffer ≥20 m but full protection against thermal change requires buffers ≥30 m; (6) large woody debris (LWD) has been poorly studied but we infer a buffer width equal to the height of mature streamside trees (~30 m) can provide natural input levels; (7, 8) macroinvertebrate and fish communities, and their instream habitat, remain near a natural or semi‐natural state when buffered by ≥30 m of forest. Overall, buffers ≥30 m wide are needed to protect the physical, chemical, and biological integrity of small streams.     

PRESENCE AND DISTRIBUTION OF CHLORINATED ORGANIC COMPOUNDS IN STREAMBED SEDIMENTS,NEW JERSEY1

ABSTRACT: Concentrations of 18 hydrophobic chlorinated organic compounds in streambed sediments from 100 sites throughout New Jersey were examined to determine (1) which compounds were detected most frequently, (2) whether detection frequencies differed among selected drainage basins, and (3) whether concentrations differed significantly among selected drainage basins. Twelve drainage basins across New Jersey that contain a range of land-use patterns and population densities were selected to represent various types and degrees of development. To ensure an adequate number of samples for statistical comparison among drainage basins, the 12 selected basins were consolidated into seven drainage areas on the basis of similarities in land-use patterns and population densities. Additionally, data for three classes of chlorinated organic compounds in streambed sediments from 255 sites throughout New Jersey were examined to determine whether the presence of these compounds in streambed sediments is related to the type and degree of development within the drainage area of each sampling site. Chlorinated organic compounds detected most frequently within the seven representative drainage areas were DDT, DDE, DDD, chlordane, dieldrin, and PCBs. DDT, DDE, and DDD, which were the most widely distributed organic compounds, were detected in about 60 to 100 percent of the samples from all drainage areas but one (where the detection rate for these compounds was about 20 to 40 percent). Chiordane and dieldrin were detected in about 80 to 100 percent of samples from highly urbanized and populated drainage areas; detection frequencies for these compounds tended to be smaller in less developed and populated areas. PCBs were detected in about 40 to 85 percent of samples from all drainage areas; detection frequencies were highest in the most heavily developed and populated areas. Analysis of variance on rank-transformed organic compound concentrations normalized to sediment organic carbon content was used to evaluate differences in concentrations among the seven representative drainage areas. Chlordane and PCBs were the chlorinated organic compounds with the most highly elevated concentrations in streambed sediments across the State. Median normalized concentrations of all six of the most frequently detected chlorinated organic compounds were highest in the most heavily urbanized and populated drainage area and lowest in the less populated, predominantly agricultural or forested areas. Concentrations of DDT and DDE, however, did not differ significantly among most of the drainage areas. Concentrations of DDD, chlordane, dieldrin, and PCBs differed significantly among drainage areas. The highest median normalized concentrations were found in samples from the most heavily urbanized and populated areas, and the lowest were in samples from the least developed, most heavily forested area. Logistic regression was used to examine relations between the presence of hydrophobic chlorinated organic compounds in streambed sediments at specified concentrations and variables that characterize the type and degree of development within the drainage areas of 255 sites across New Jersey. The explanatory variables found most useful for predicting the presence of chlorinated organic compounds in streambed sediments include total population and amounts (in square kilometers) of various land-use categories. Logistic regression equations were developed to identify significant relations between population and amounts of specific land-use categories within drainage areas and the probability of detecting chlorinated organic contaminants in streambed sediments. These relations can be used to assist in the identification of geographic regions of primary concern for contamination of bed sediments by chlorinated organic compounds across the State.     

HYDROLOGICAL EFFECTS OF AN UNCONTROLLED FLOWING WELL,RED RIVER VALLEY,NORTH DAKOTA,USA1

ABSTRACT: In areas of the Red River Valley that overlie permeable Paleozoic sediments, wetlands and salinization have developed where unregulated flowing wells discharge brackish water. Field data were collected to assess the fate of water and salt from a well 25 km northwest of Grand Forks. Drilled during the drought of the 1930s, discharge was used to replenish water in a small oxbow pond used by livestock. The unregulated well discharges about 56 m³/day, measured since 1993. This discharge exceeds ground water flow from the site, thereby forming a ground water mound with a maximum height of 1 m and a diameter of about 300 m. Most soil and underlying sediments near the well have a hydraulic conductivity of 0.3 m³/day. Flow net analysis suggests that less than 25 percent infiltrates, with the remaining water lost to surface flow and evapotranspiration (ET). Evapotranspiration and slow infiltration has led to increased salinization, with shallow soils exhibiting EC to 500 milliSiemens/m. The most pronounced soil salinization occurs along the margins of the oxbow pond and meander scars. Wetland vegetation with low diversity comprises three zones, with species associations similar to those of closed basin prairie potholes to the west.     

Metal and oxalate contamination in a suburban watershed in the greater Toronto area: the benefits of combining acid leach and selective extraction procedures

Environmentally available concentrations of Fe, Mn, Zn, Cu, Pb, Cr and Ni in soils and sediments from a small suburban catchment, obtained using an acid leach procedure, are compared to the Ontario Ministry of the Environment lowest effect level (LEL) and severe effect levels (SEL) and to Provincial sediment quality guidelines (PSQG's). These data are then compared to the bioavailability, potential bioavailability and non-bioavailability of the same metals, plus oxalate concentration, identified using a selective extraction procedure. This combination of techniques enhanced analytical interpretation with respect to metal mobility and potential metal contamination. Selective extraction highlighted the presence of oxalate as a potential contaminant, especially in poorly drained valley floor deposits (33,633 mg kg(-1) and 26,284 mg kg(-1)) and lakeshore sediments (27,095 mg kg(-1) and 13,729 mg kg(-1)). These levels are considerably in excess of those previously documented in a similar study from Rio de Janeiro, where contamination of urban sediment by sewage is a recognised environmental problem, and could possibly be used both as an indicator of similar contamination and the identification of those areas that warrant further investigation.     

西溪湿地底泥质量现状与生态风险初步评价

为了解西溪湿地底泥质量现状,2012年9月采集保护区内不同干扰类型的底泥样本,测试了底泥中重金属和POPs中PCBs、OCPs和PAHs的含量,并对湿地底泥污染进行了生态风险初步评价。结果表明,底泥中未检出PCBs和OCPs,但检测出14种EPA优控PAHs,总PAHs的浓度范围为115.9～217.8 ng·g^-1,低于潜在生态风险的效应区间低值ERL,其中列入中国＂水中优先控制污染黑名单＂的7种PAHs均有检出并且其总量占∑PAHs 1/2左右（平均为50.08%）;底泥中8种重金属含量平均值低于《土壤环境质量标准》（GB 15618—1995）的二级标准,但Hg、Zn、Pb、Ni含量在多个位点已超过一级标准;分别采用土壤背景值和国家一级标准为参比值对湿地底泥中重金属进行单因子污染风险指数评价,发现分别有7种和4种元素的污染指数大于1;综合分析不同干扰类型的底泥质量,发现底泥疏浚能有效降低有机质含量、全氮和PAHs含量,但对全磷、重金属含量则无明显效果,封闭水体的干塘措施能显著减少污泥量和有机物含量。研究结果表明,西溪湿地底泥中高环PAHs和重金属污染水平可能对西溪湿地生物具有潜在的生物毒性作用及不利的生态影响效应,其疏浚底泥农用则无生态风险。     

A washing procedure to mobilize mixed contaminants from soil: I. Polychlorinated biphenyl compounds

We conducted a laboratory study to assess the feasibility of a washing process with nonionic and anionic surfactants in combination with ethylenediaminetetraacetate (EDTA) for the simultaneous mobilization of heavy metals and polychlorinated biphenyls (PCBs) from a field-contaminated soil. Unit processes consisting of complexometric extraction and surfactant-assisted mobilization were combined with reagent regeneration and detoxification steps to generate innocuous products. Ten minutes of ultrasonic mixing of the soil with a combination of 30 mL L(-1) surfactant suspension and a sparing quantity (2 mmol) of EDTA mobilized appreciable quantities of PCBs, virtually all of the available Cd, Cu, Mn, and Pb, and lesser amounts of the Zn, Ni, and Cr but only small quantities of Al and Fe. Relative to individual reagents, combinations of surfactant (Brij 98, Triton X-301, or Triton XQS-20) with EDTA did not influence PCB extraction efficiencies perceptibly. Of the three surfactants, the Brij 98 proved to be the most efficient for three successive extractions with a single charge, mobilizing 83% of the PCBs, whereas companion extractions that used fresh reagent each time mobilized 87% of the soil PCB content. The decreased PCB mobilization with the same quantity of anionic surfactant (71 or 68%) resulted from losses during the EDTA regeneration process with zero-valent Mg. In toto, these studies demonstrate that PCB compounds and selected heavy metals can be coextracted efficiently from soil with three successive washes with the same washing suspension containing EDTA and a nonionic surfactant.     

高脂肪样品中PCBs和OCPs分离方法研究

研究开发了用于分离高脂肪样品中21种多氯联苯（PCBs）和22种有机氯农药（OCPs）的分离柱填料,以及利用该填料分离含脂肪的动物组织样品中PCBs或OCPs的方法。该填料按质量百分比由硅胶-弗罗里硅土混合物30%-35%、酸性改性硅胶50%-60%和无水硫酸钠10%-15%组成,并使用自主研发的四通道色谱分离仪对样品进行分离和净化。利用本方法的填料分离PCBs或OCPs,分离方法高效、快速、工艺简单,可在成本较低的条件下达到显著的分离效果。PCBs化合物柱回收率可达96.4%-119%,对鱼脂肪组织加标回收率可达74.4%-100%;OCPs化合物柱回收率可达78.4%-103%,对鱼脂肪组织加标回收率可达78.3%-102%。结果表明该填料可用于分离PCBs或OCPs,色谱分离效果良好,可以满足高脂肪样品中OCPs和PCBs的监测分离需要。