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1.

Purpose

The purpose of this study was to elucidate historical trends, spatial variations, and the sources of polycyclic aromatic hydrocarbons (PAHs) pollution in several Japanese lakes.

Materials and methods

The vertical distributions of PAHs in the core samples of sediments taken at several points in lakes Kasumigaura, Suwa, Kizaki, and Shinji were determined using a gas chromatograph equipped with a mass selective detector and combined with chronological information and the physical/elemental properties of the sediment.

Results and discussion

Seventeen related compounds (congeners) typically had concentration peaks at sediment depths corresponding to the 1960s to 1970s. In Lake Shinji and one bay of Lake Kasumigaura, there was a tendency for PAH concentrations to increase downstream; in contrast, another bay of Lake Kasumigaura showed the reverse trend. During big flood events, the fluxes of PAHs increased due to large inputs of particulate matter, although PAH concentrations were reduced. For the four study lakes and other similar lakes, PAH concentrations of surface sediments were approximately proportional to population densities in the respective watersheds, while the total input of PAHs to the lakes were correlated with their population and watershed area. The source apportionment analysis using isomer ratios for the congener profiles indicated that the principal sources of the PAHs in the lake sediments were gasoline and/or diesel engine exhausts and biomass burning.

Conclusions

The observed concentration peaks showed a deterioration of the chemical quality of atmospheric conditions around 1960?C1970 and a recent tendency for their amelioration. Between-lake differences suggest that the influence of human activity in the watersheds influences sediment PAH concentrations. The PAH sources were identified to be of pyrogenic origin.  相似文献   

2.

Purpose

Understanding the fate and behavior of polycyclic aromatic hydrocarbon (PAH) sources in aquatic systems is important for the efficiency of control policies. In this work, a new approach??organic carbon-normalized sediment?Cpore water partition coefficients of PAH source contributions (logK??Osource)??was developed to study the sediment?Cpore water partition of PAH source contributions. The focus of this study was the Yellow River, which is the second largest river in China and one of the largest rivers in the world.

Materials and methods

Sixteen priority US Environmental Protection Agency PAHs were analyzed in 14 surface sediments and 11 pore water samples. Principal component analysis?Cmultiple linear regression (PCA-MLR) and Unmix models were employed to estimate the source contributions of PAHs in sediments and pore water samples. Finally, logK??Osource values were calculated according to the modeled source contributions of PAHs.

Results and discussion

??PAHs (sum of the 16 PAH concentrations) in 14 sediment samples and 11 pore water samples from the Yellow River were 1,415?±?726?ng?g?1 dry weight (dw) and 123?±?57.4???g?l?1, respectively. The source apportionment results indicate the following: (1) for sediment samples, the contributions to ??PAHs from vehicular emissions, coal combustion, and petrogenic sources were 41.07?C61.05, 38.83?C45.56, and 11.18?C14.92?%, respectively, and (2) for pore water samples, vehicular emissions were the most significant contributor (45.51?C69.39?%), followed by petrogenic sources (29.80?C34.22?%) and coal combustion (7.35?C21.59?%). Coal combustion had the highest logK??Osource values (4.15?C4.26) among the three categories, followed by vehicular emissions (3.51?C3.57) and petrogenic sources (3.30?C3.43).

Conclusions

The possible categories of PAH sources identified by hierarchical cluster analysis, PCA-MLR, and Unmix models were consistent, indicating that vehicular emissions, coal combustion, and petrogenic sources were three important categories. The logK??Osource values indicate that contributions from coal combustion had a higher partition for the sediment phase compared with the other two source categories.  相似文献   

3.

Goal, Scope and Background

Distribution of hydrophobic organic contaminants in abiotic compartments is essential for describing their transfer and fate in aquatic ecosystems. Taihu Lake is the third largest freshwater lake in China. Water quality of Taihu Lake has deteriorated greatly during the last decades and has threatened the water supply. The aim of the present study was to investigate the partitioning of polycyclic aromatic hydrocarbons (PAHs) among overlying water, suspended particulate matter (SPM), sediments, and pore water in Meiliang Bay, Taihu Lake and to provide useful information for the ecological engineering in this area.

Materials and Methods

Overlying water and surface sediment were sampled from six sites in Meiliang Bay, Taihu Lake, China. Within 72 h of sampling, sediments were centrifuged to obtain the pore water. Overlying water samples were filtered to separate dissolved and SPM samples. After extraction, samples were purified following a clean-up procedure. PAH fraction was obtained by elution with a mixture of hexane: DCM (7:3, V/V) and analyzed by GC/MS.

Results

PAHs concentrations in overlying water varied from 37.5 ng/L to 183.5 ng/L. Concentrations of PAHs in pore water were higher than those in overlying water. The total concentrations of 16 priority PAHs in sediments ranged from 2091.8 ng/g-dw to 4094.4 ng/g-dw. PAHs concentrations on SPM were decreased with suspended solid concentrations (SSC). Total PAHs concentrations on SPM varied in the range of 3369.6 ng/g-dw to 7531.1 ng/g-dw. The partition coefficients between sediment and overlying water (log K oc) for PAHs with log K ow<5 were positively correlated with their octanol-water partition coefficients (log K ow) (n=39, r=0.79, p<0.0001). Partition coefficients between sediment and pore water (log K oc′) for all PAHs were also significantly correlated with their log K ow values (n=48, r=0.82, p<0.0001).

Discussion

In general, PAHs derived from combustion sources tend to bind strongly to soot particles in natural sediment. Consequentially, K oc values observed in the natural environment could be orders of magnitude higher than those predicted by linear correlation relationships under laboratory conditions. In the present study, the ratio of log K oc values to log K ow values falls consistently above 1, indicating that the sediment soot carbon in the bay was more attractive for PAHs than n-octanol. The log K oc′ was also higher than that predicted under laboratory conditions, suggesting that the measured pore water PAH concentrations were lower than those predicted. That is to say, not all the sediment PAHs can be available to partition rapidly into sediment pore waters. A variation in soot content is a possible reason. Furthermore, concentrations of PAHs on SPM were higher than those in sediments. The compositions of PAHs on SPM and in sediments were similar, indicating the importance of re-suspension process of sediments in the partitioning process of the shallow lake.

Conclusions

The results indicated the equilibrium partitioning model could be used to predict PAHs distribution in various phases of a shallow lake in the stagnation period, but re-suspension processes should be considered to modify the relationship between log K ocs and log K ows.

Recommendations and Perspectives

Concentration, particle size and composition of resuspended particles could affect the relationship between log K ocs and log K ows. Further work should be done under field conditions, especially where a steady thermodynamic equilibrium state could be assumed.
  相似文献   

4.

Purpose

Polycyclic aromatic hydrocarbons (PAHs) are unintentional products that are classified as persistent toxic substances. The goal of the present study was to generate data on the presence of 15 priority PAHs that are found in surface sediment and core sediment in the region of the Turvo/Grande watershed, São Paulo State, Brazil, which is an area of expanding sugarcane cultivation, and to correlate these data with the sources of these PAHs and the guiding values for sediment quality analysis.

Materials and methods

Surface sediments and sediment cores were sampled during the rainy and dry seasons in February and July 2010. The extraction of PAHs from sediments was performed using a Soxhlet extractor, and then the extract was cleaned according to the methods of the US EPA 3630C (US EPA 1996) using a silica gel column. Quantification was performed using high performance liquid chromatography with fluorescence detection.

Results and discussion

The concentrations of all 15 PAHs decreased as the depth of the sediment core increased. Overall, the concentrations decreased along the sediment core; however, the RTURARG (region predominantly used for planting sugarcane and livestock) during the rainy season and the CAPRP sampling site (located at part of the Preto River dam) during the dry season showed increased concentrations in the first few sediment fractions, and then the concentrations decreased. Higher concentrations were observed in urban locations, and the concentration of naphthalene was higher than the probable effect level (PEL) determined by the Canadian environmental agency. The obtained diagnostic ratios indicate that the sediment from areas with an abundance of sugarcane was a pyrolytic source of PAHs, which indicates a contribution from burning straw to the PAH concentrations in those areas.

Conclusions

For all sampling sites and all PAHs, we found a decreasing trend in PAH concentrations with increasing sediment core depth, and the locations, such as CAPRP, that experienced a higher level of human activity had the highest total concentrations of PAHs. These locations were the only areas in which the PAH naphthalene was found in higher concentrations than the PEL. The diagnostic ratios reveal that regions with sugarcane plantations had predominantly pyrolytic sources of PAHs, indicating the contribution of PAHs from sugarcane straw burning.
  相似文献   

5.

Purpose

We employ a geochemical-fingerprinting approach to estimate the source of suspended sediments collected from tributaries entering Falls Lake, a 50-km2 drinking water reservoir on the Neuse River, North Carolina, USA. Many of the major tributaries to the lake are on North Carolina’s 303(d) list for impaired streams, and in 2008, the lake was added to that list because of high values of turbidity, likely sourced from tributary streams.

Materials and methods

Suspended sediments were collected from four streams with a time-integrated sampler during high-flow events. In addition, composite sediment samples representing potential sources were collected from stream banks, forests, pastures, construction sites, dirt and paved roads, and road cuts within tributary basins. Radiocarbon dating and magnetic susceptibility measurements were used to determine the origin of stream bank alluvial deposits. Sediment samples were analyzed for the concentrations of 55 elements and two radionuclides in order to identify tracers capable of distinguishing between potential sediment sources. The relative sediment source contributions were determined by applying a Monte Carlo simulation that parameterized the geochemical tracer data in a mixing model.

Results and discussion

Radiocarbon and magnetic susceptibility measurements confirmed the presence of “legacy” sediment in the Ellerbe and New Light Creek valley bottoms. Mixing model results demonstrate that stream bank erosion is the largest contributor to the suspended sediment load in New Light Creek (62%), Ellerbe Creek (58%), and Little Lick Creek (33%), and is the second largest contributor in Lick Creek (27%) behind construction sites (43%).

Conclusions

We find that stream bank erosion is the largest nonpoint source contributor to the suspended sediment load in three of the four catchments and is therefore a significant source of turbidity in Falls Lake. The presence of legacy sediment appears to coincide with increased contributions from stream bank erosion in Ellerbe and New Light creeks. Active construction sites and timber harvesting were also significant sources of suspended sediment. Water quality mitigation efforts need to consider nonpoint-source contributions from stream bank erosion of valley bottom sediments aggraded after European settlement.  相似文献   

6.

Purpose

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous and persistent contaminants in aquatic bed sediments. A better understanding of their in-bed fate and transport is therefore key in minimising the risk to the environment over time through various remediation and monitoring strategies. Since ecological effects and risks are related to contaminant concentrations, this study developed CoReTranS, a predictive model that simulates one-dimensional organic contaminant reaction and transport in bed sediments.

Materials and methods

CoReTranS was benchmarked against analytical solutions of simplified reactive transport models and validated using a published study of marsh sediments contaminated with petroleum-derived hydrocarbons from Wild Harbour, West Falmouth, MA, USA.

Results and discussion

The CoReTranS model effectively predicted the vertical distribution of PAHs in the Wild Harbour sediments as confirmed by the modelling results from the published study. The CoReTranS model was also used to interpret results from a published study of PAH-contaminated fjord sediments from Kitimat Arm in British Columbia, Canada. Specific insights into the post-depositional fate and transport of selected PAHs in the Kitimat fjord sediments were obtained by comparing the measured concentration-depth profiles with the numerical results from the CoReTranS model. Key parameters such as effective diffusivity of contaminants and burial velocities of sediment particles were shown to possibly account for the predicted concentrations-depth profiles in the Kitimat fjord sediments.

Conclusions

As demonstrated, CoReTranS can simulate reactive transport models in order to predict PAH concentration profiles in porewater under site-specific conditions. The information derived from the use of the CoReTranS model highlighted practical application of such information by engineers to site-specific risk assessment and remediation.  相似文献   

7.

Purpose

The management of sediments from stormwater infiltration basins is nowadays a key issue for local authorities to ensure long-term performance. Speciation of pollutants is particularly required in view of reuse of these materials. If fractionation of trace metals in sediments is relatively well described, polycyclic aromatic hydrocarbons (PAHs) speciation was only studied using particle size distribution. Therefore, this study aims at the characterization of the PAHs-bearing fractions in sediments.

Materials and methods

Three sediments with various physicochemical properties were sampled in the west and north of France to characterize the distribution of PAHs among organic and inorganic components. Respective organic and inorganic matrixes were obtained by alkaline extraction and methyl isobutyl ketone (MIBK) fractionation procedure. The nature of the solid fractions was assessed through microanalyses: infrared spectroscopy (Fourier transform infrared spectroscopy), X-ray diffraction (XRD), and scanning electron microscopy with X-ray spectroscopy. Bulk sediments and extracted fractions were analyzed for organic matter parameters: elemental analysis (C, N, and H), total organic matter, total organic carbon, hydrocarbons (C10–C40), and PAHs.

Results and discussion

The characterization of bulk sediments highlighted that they were mainly composed of single particles, originating from the geological background, and aggregates (10 to 300 μm) composed of minerals and large organic matter content. The C/N ratio and PAH ratios were shown to be helpful for the determination of the natural or anthropogenic origin of organic matter or to evaluate additional contribution of industrial activities. The fractionation results underlined the role of the aggregates on the distribution of PAHs. Humin fraction and bound-humic acids were mainly composed of aggregates (10 to 150 μm) and accounted for 60 to 70 % of sample mass. The PAHs are mainly sequestrated in these fractions. Only up to 1 % of PAHs are adsorbed on the mineral fraction.

Conclusions

Both alkaline extraction and MIBK procedure demonstrated that PAH residues were readily sequestrated in humin and bound-humic acids fractions and that fulvic acids, humic acids, and mineral fractions contained poor concentrations of PAHs. Microanalyses underlined the high level of aggregation of particles in sediments and their mixed inorganic and organic nature. In case of stormwater sediments, the location of PAHs in highly organic aggregates is consistent with their sources, being both oil products and debris from vehicles and road.  相似文献   

8.

Purpose

A major challenge to phytoremediation of co-contaminated soils is developing strategies for efficient and simultaneous removal of multiple pollutants. A pot experiment was conducted to investigate the potential for enhanced phytoextraction of cadmium (Cd) by Sedum alfredii and dissipation of polycyclic aromatic hydrocarbons (PAHs) in co-contaminated soil by application of pig manure vermicompost (PMVC).

Materials and methods

Soil contaminated by Cd (5.53?mg?kg?1 DW) was spiked with phenanthrene, anthracene, and pyrene together (250?mg?kg?1 DW for each PAH). A pot experiment was conducted in a greenhouse with four treatments: (1) soil without plants and PMVC (Control), (2) soil planted with S. alfredii (Plant), (3) soil amended with PMVC at 5?% (w/w) (PMVC), and (4) treatment 2?+?3 (Plant?+?PMVC). After 90?days, shoot and root biomass of plants, Cd concentrations in plant and soil, and PAH concentrations in soil were determined. Abundance of PAH degraders in soil, soil bacterial community structure and diversity, and soil enzyme activities and microbial biomass carbon were measured.

Results and discussion

Application of PMVC to co-contaminated soil increased the shoot and root dry biomass of S. alfredii by 2.27- and 3.93-fold, respectively, and simultaneously increased Cd phytoextraction without inhibiting soil microbial population and enzyme activities. The highest dissipation rate of PAHs was observed in Plant?+?PMVC treatment. However, neither S. alfredii nor PMVC enhanced PAH dissipation when applied separately. Abundance of PAH degraders in soil was not significantly related to PAH dissipation rate. Plant?+?PMVC treatment significantly influenced the bacterial community structure. Enhanced PAH dissipation in the Plant?+?PMVC treatment could be due to the improvement of plant root growth, which may result in increased root exudates, and subsequently change bacterial community structure to be favorable for PAH dissipation.

Conclusions

This study demonstrated that remediation of Cd and PAHs co-contaminated soil by S. alfredii can be enhanced by simultaneous application of PMVC. Long-term evaluation of this strategy in co-contaminated field sites is needed.  相似文献   

9.

Purpose

This study addresses the feasibility of a flotation technique, using a lab-scale flotation cell, to simultaneously remove both metals and polyaromatic hydrocarbons (PAHs) from fine sediment fractions (<250 μm) that are potentially contaminated with copper (Cu).

Materials and methods

A multiple flotation process with three consecutive flotation stages was performed on three sediments (13S, 14B, and 24A) with different particle size distributions, Cu and PAH concentrations, and organic matter contents.

Results and discussion

Flotations performed under selected conditions allowed for significant removal of both Cu (61–70 %) and PAHs (75–83 %) with acceptable froth recoveries of approximately 23–29 %. Removal rates for arsenic, lead, and zinc were 48–61, 40–48, and 32–36 %, respectively. Flotation selectivity of Cu was greatly influenced by the contents of fine particles and organic matter of the sediments. The maximum flotation selectivity was obtained for the 53–125-μm size fraction. The high flotation selectivity of Cu (2.5–3.2) and PAHs (3.0–3.6) demonstrated the feasibility of flotation to treat soils or sediments containing both organic and inorganic pollutants.

Conclusions

Overall, the flotation results showed a high selectivity for both Cu and PAHs and demonstrated the feasibility of flotation to treat media contaminated with organic and inorganic contaminants.  相似文献   

10.

Purpose

A comprehensive study was conducted to investigate the presence of polycyclic aromatic hydrocarbons (PAHs) in Dongjiang River Basin (DRB) soils and to evaluate their sources and ecological and health risk. In addition, factors affecting the distribution and fate of PAHs in the soils such as emission density, soil organic matter, degradation, etc. were studied.

Materials and methods

Surface soil (0–20 cm) samples from 30 sampling sites in the rural areas of DRB were collected and analyzed for 17 polycyclic aromatic hydrocarbons (16 EPA priority PAHs and perylene). Positive matrix factorization model was used to investigate the source apportionment of these PAHs, and an incremental lifetime cancer risk (ILCR) was used to estimate the integrated lifetime risks of exposure to soil-borne PAHs through direct ingestion, dermal contact, and inhalation collectively.

Results and discussion

The total PAH concentrations in the rural soils in DRB range from 23.5 to 231 μg/kg with a mean concentration of 116 μg/kg. The predominant PAHs in the rural soils were naphthalene, fluoranthene, phenanthrene, and benzo(b)fluoranthene. Cluster analysis was performed to classify the soil PAHs into three clusters, which could be indicative of the soil PAHs with different origins and different properties. Source apportionment results showed that coal, biomass, oil, commercial creosotes, and vehicle contributed 24 %, 24 %, 17 %, 17 %, and 18 % of the total soil PAH burden, respectively. The ILCR results indicated that exposure to these soil-borne PAHs through direct ingestion, dermal contact, and inhalation collectively produces some risk.

Conclusions

PAHs in the soils of the DRB will produce long-term influences on rivers and oceans via soil erosion and river transport. Therefore, PAHs in rural soils of DRB have potential impacts on the water supply and human health risk.  相似文献   

11.

Purpose

The importance of the bioaccessible fractions of particle-bound contaminants is a key feature for the assessment of their likely risks to the aquatic environment. The present study investigated the extractability and potential toxicity of polycyclic aromatic hydrocarbons (PAHs) in river sediments. This study combined chemical with bioanalytical tools to establish a more in-depth insight into the relationship between the extractability of sediment contaminants, the chemodynamic properties of each extraction approach, and resulting toxicity.

Materials and methods

Sediment samples were treated with different extraction methods, namely Soxhlet extraction with acetone (SOX), membrane dialysis extraction (MDE) with n-hexane, ultrasonic extraction with acetone (USE), and extraction with (2-hydroxpropyl)-??-cyclodextrin (HBCD). The extracts were analyzed for PAHs using gas chromatography/mass spectrometry and tested using the neutral red retention assay and the ethoxyresorufin-O-deethylase (EROD) induction assay with the permanent fish cell line RTL-W1.

Results and discussion

The SOX and MDE approaches were comparable in their extraction power regarding PAHs and their cytotoxicity. However, the EROD activity differed between SOX and MDE, possibly due to retardation effects of the polyethylene membrane used in MDE. Thus, macromolecular components of the sediment were not extracted and therefore did not contribute to toxicity. HBCD extraction provided 3.4?% of the total PAH content in the sediments and might be an appropriate approach to predict the bioaccessible fraction. USE showed an extraction power between the HBCD approach and the MDE as well as SOX and MDE method. Hence, USE is neither appropriate for exhaustive extraction nor for biomimetic extraction.

Conclusions

MDE and SOX have been approved for the exhaustive extraction of PAHs from sediments for a worst case assessment of effect potentials. The influence of the low-density polyethylene membrane and the experimental conditions on the diffusion of compounds with broad physical?Cchemical properties, and the establishment of models such as quantitative-structure relationships for the prediction of diffusion behavior of a broad range of compounds require further assessment. HBCD was confirmed as a method providing a certain, putatively bioaccessible, fraction. Mechanistic research is required regarding desorption and uptake kinetics of particularly bound compounds with different physical?Cchemical properties in the solid phase?Cwater?CHBCD system to get more insight in the underlying partitioning processes.  相似文献   

12.

Purpose

During the late 1950s and early 1960s, industrial waste material highly enriched with various contaminants (e.g., heavy metals, polycyclic aromatic hydrocarbons (PAHs)) was dumped in the inner Bay of Mecklenburg, western Baltic Sea. Between 2002 and 2004, a research program was initiated using chemical analysis in combination with bioanalytical techniques to assess the extent and variability in contamination at this dump site (DS). The data were compared to a reference area (RS) with similar environmental conditions, which is representative of the western Baltic Sea.

Materials and methods

Twelve PAHs were investigated to assess their ecological hazard, as they were identified as major pollutants in the dumped material. In addition to analyzing the actual PAH contamination status in the sediments, PAHs measured in the soft tissue of Arctica islandica were also used as an indicator of contaminant bioaccumulation. A biotest battery was applied to determine the toxic effects of contaminants in the sediment.

Results and discussion

Significantly elevated PAH concentrations (sum of 12 PAHs) of ～3,000 ng g?1 dw and higher bioaccumulation factors (BAFs) were determined in the soft body tissue of A. islandica collected at DS (t test, p?=?0.025). The results also showed that the sediment PAH contamination was significantly higher at DS (1,952–5,466 ng g?1 dw) than at RS (1,384–2,315 ng g?1 dw). The results revealed a major heterogeneity in the PAH concentration at DS due to an attempt to cover the toxic material with clean clay. This resulted in a more heterogeneous distribution of the dump material rather than covering it up completely. However, not all relevant contaminants were included in this study, not only because it is too costly to determine them all but also because unidentified contaminants present at concentrations below the limit of detection cannot be measured. Bioassays were used to fill this gap in the hazard assessment in a cost-effective way by investigating the possible effects of sediment contamination on benthic organisms. The results showed a high variability and magnitude of growth and luminescence inhibition. Bacterial contact tests with marine organisms showed a high toxicity response (>80 % inhibition) from DS sediments. In contrast, the luminescent bacteria test (Vibrio fischeri) showed equivalent effects of sediments from both DS and RS.

Conclusions

The spatial distribution of toxicity in DS, the bioaccumulation in mussels and the analytical evidence of PAH pollution clearly show that the dumped material still represents a potential risk even after 60 years.  相似文献   

13.

Purpose

Excess nutrients such as phosphorus (P) transported from the Everglades Agricultural Area (EAA) in South Florida, USA, to downstream water bodies have been identified as contributing to trophic imbalances within the Florida Everglades. Decades of farming drainage from the EAA has led to accumulation of sediments in regional canals which may be transported to downstream ecosystems and act as potential internal source of P.

Materials and methods

Intact sediment cores were collected from three main conveyance and three farm canals within the EAA. Physicochemical assessment, mineralogy, P speciation, and storage were determined for surface and subsurface layers.

Results and discussion

The main conveyance canal sediments had higher total P (TP) concentrations (1,280?±?360?mg?kg-1) than the farm canals (960?±?540?mg?kg-1), while farm canal sediments showed higher organic matter content (28?C53?%) compared to the main canal (24?C27?%) sediments. The minerals found in main conveyance canal sediments were similar to those found in Lake Okeechobee. The labile KCl?CP fraction comprised <2?% of TP from all canal sediments, while NaOH?CPi (i?=?inorganic) fraction consisted of 1?C14?% of TP. The majority of P in the canal sediments was contained in the HCl?CP fraction (Ca?CP and Mg?CP), comprising >50?% of TP in the main and farm canal sediments. An estimated 73 metric tons (mt) of P was stored in the 0?C10-cm layer of the three main conveyance canals within the EAA boundary of which 57-mt P is reactive and potentially available for release at different time scales.

Conclusions

The EAA canal sediments are highly organic with low bulk density and susceptible of being transported to downstream ecosystems. Many factors can impact the potential release of the reactive stored P, including redox potential of sediments as well as the overlying water column P concentration. Further investigation of potential P release from these sediments is warranted.  相似文献   

14.

Purpose

Polycyclic aromatic hydrocarbons (PAHs) are largely accumulated in soils in China. The immobilized-microorganism technique (IMT) is a potential approach for abating soil contamination with PAHs. However, few studies about the application of IMT to contaminated soil remediation were reported. Due to recalcitrance to decomposition, biochar application to soil may enhance soil carbon sequestration, but few studies on the application of biochars to remediation of contaminated soil were reported. In this study, we illustrated enhanced bioremediation of soil having a long history of PAH contamination by IMT using plant residues and biochars as carriers.

Materials and methods

Two PAH-degrading bacteria, Pseudomonas putida and an unidentified indigenous bacterium, were selected for IMT. The extractability and biodegradation of 15 PAHs in solution and an actual PAH-contaminated soil amended with immobilized-bacteria materials were investigated under different incubation periods. The effects of carriers and the molecular weight of PAHs on bioremediation efficiency were determined to illustrate their different bio-dissipation mechanisms of PAHs in soil.

Results and discussion

The IMT can considerably enhance the removal of PAHs. Carriers impose different effects on PAH bio-dissipation by amended soil with immobilized-bacteria, which can directly degrade the carrier-associated PAHs. The removal of PAHs from soil depended on PAH molecular weight and carrier types. Enhanced bio-dissipation by IMT was much stronger for 4- and 5-ring PAHs than for 3- and 6-ring ones in soil. Only P400 biochar-immobilized bacteria enhanced bio-dissipation of all PAHs in contaminated soil after a 90-day incubation.

Conclusions

Biochar can promote bioremediation of contaminated soil as microbial carriers of IMT. It is vital to select an appropriate biochar as an immobilized carrier to stimulate biodegradation. It is feasible to use adsorption carriers with high sorptive capabilities to concentrate PAHs as well as microorganisms and thereby enhance dissipation of PAHs and mitigate soil pollution.  相似文献   

15.

Purpose

One of the central issues related to global changes in weather is the increasing occurrence of flood events that can result in the re-suspension of contaminated sediments in rivers. Here, we report on a proof-of-concept study combining hydraulic engineering and ecotoxicology in a new interdisciplinary approach to assess the toxicity of re-suspended polluted sediments after a simulated flood event.

Materials and methods

Rainbow trout (Oncorhynchus mykiss) were exposed for 5 days under simulated flood conditions in an annular flume with artificial sediments that were spiked with a mixture of polycyclic aromatic hydrocarbons (PAH) at environmentally relevant concentrations. Specifically, the objective of this study was to bridge the gap between the physical re-suspension of pollutants and resulting toxicological impacts on aquatic organisms. A suite of different molecular, biochemical and histological markers was used to test the hypothesis that re-suspension of sediments can lead to re-mobilization of PAHs and subsequently to effects on aquatic organisms.

Results and discussion

The micronucleus frequency was significantly 4.3-fold elevated after exposure. There was no significant indication of Aryl hydrocarbon receptor signaling (no EROD induction or increased CYP1A protein content, only slight induction of CYP1A gene expression). Biliary metabolite concentration was the most sensitive marker of PAH exposure. Results for other biomarkers (glutathione-S-transferase, catalase and lipid peroxidation) were inconclusive.

Conclusions

In combination with chemical analyses of suspended matter, the presented approach will be used to improve understanding of the re-mobilization of pollutants from sediments in support of environmental risk assessment.  相似文献   

16.
Specific stability of organic matter in a stormwater infiltration basin   总被引：1，自引：0，他引：1  

Purpose

In stormwater infiltration basins, sediments accumulate at the soil surface and cause a gradual filling up of soil pores. These sediments are composed of a mixture of natural and anthropogenic (as oil products) organic matters (OMs). The degradation kinetics of these sediment OMs and their biological stability has been neglected. This study aimed to characterize sediments OMs to assess their evolution and their capacity to degrade.

Materials and methods

To characterize OMs from the sediment layer, we measured at several places in the infiltration basin, total OM and carbon (C) contents, C distribution and biochemical fractions of the OM in the different size fractions, the sediment’s C mineralization potential, soil microbial biomass, and organic pollutants (polycyclic aromatic hydrocarbons (PAHs)) in the sediment layer.

Results and discussion

OM contents were high and varied from 66 to 193 g?kg?1 from the inlet to the outlet of basin. Depending on rainfall intensity and volume, organic particles were deposited at varying distances in the basin by decantation; this was confirmed by analysis of sediment C distribution in the different size fractions. Despite high amounts of OM, organic C had a low biodegradability. Mineralization potentials were low compared to natural soil (i.e., from 0.3 to 1.1 g CO2–C kg?1 total organic carbon). Biochemical fractionation of the organic fractions indicated that they were mainly composed of a soluble fraction, which contributed to reducing OM biodegradability. The activity of the sediment microbial biomass was low. PAH contents seemed to be partly responsible for the high biostability of OMs.

Conclusions

There was limited capacity for biodegradation of sediment OMs probably due to inhibitory effects of soluble PAHs and consequently low microbial activity.  相似文献   

17.

Purpose

The Turvo/Grande drainage basin (TGDB), located in the northwestern region of S?o Paulo state, covers an area of 15,983?km2. The region is typically regarded as agricultural by the S?o Paulo State Environmental Agency, but the industrial area is expanding, and some studies have shown that metal concentrations in water can be higher than the values regulated by Brazilian law. Therefore, the aim of this study was to assess the role of sediments as a source or a sink of metals for drainage basin management.

Materials and methods

Interstitial water from different sediment depths (0?C42?cm) and the sediment?Cwater interface and sediment core samples were collected in February and July 2010 from the Preto, Turvo, and Grande rivers. Quantification of Cr, Cu, Fe, Mn, Ni, and Pb in these samples was performed by graphite furnace or flame atomic absorption spectrometry. Metal diffusive flux estimation from sediment into the overlying water was calculated by Fick??s First Law of Diffusion.

Results and discussion

The fluxes of all metals for the three rivers were positive, indicating diffusion into the overlying water. Ni and Pb showed the lowest diffusive fluxes, which ranged from 2.4 to 3,978???g?m?2?day?1 for Ni and from ?0.1 to 1,597???g?m?2?day?1 for Pb. In turn, Cu and Cr were subject to the largest transfer to water, especially in the dry season (Cr, 4.5?C7,673???g?m?2?day?1; Cu, 1.3?C14,145???g?m?2?day?1). The Preto River (urban area) showed smaller fluxes than the Grande River (agricultural area), and the values of the latter were higher than those found in other impacted areas of the world.

Conclusions

The diffusive fluxes indicate that sediments from the TGDB act as a source of metals for the water column, with increased export of metals, particularly Cr and Ni, from the sediment into the overlying water during the dry season.  相似文献   

18.

Purpose

Little information is available heretofore on the gradient distribution of persistent organic pollutants in rhizosphere on a field scale. In this field study, we seek to explore the in situ distribution gradient of polycyclic aromatic hydrocarbons (PAHs) in rhizosphere soil proximal to the roots.

Materials and methods

Clover (Trifolium pratense L.) and hyssop (Hyssopus officinalis L.) grew in situ in the contaminated field soil near a petrochemical plant and were harvested when about 30 cm tall with mature roots. Rhizosphere soils of the plants were sampled including the rhizoplane, strongly adhering soil, and loosely adhering soil. Eleven EPA-priority PAHs were detected in each layer of rhizosphere soils in proximity to the root surface.

Results and discussion

The PAH concentrations followed the descending order of bulk soil, loosely adhering soil, strongly adhering soil, and rhizoplane soil in proximity to the root surface of clover and hyssop. The rhizosphere effect (R, in percent) on PAH distribution clearly decreased with increasing distance from the root, and a more significant decrease was observed for hyssop compared to clover. R values were generally lower for three- and four-ringed PAHs in the rhizosphere, which were more significant in loosely and strongly adhering rhizosphere layers.

Conclusions

Our field observations combined with previous potted studies demonstrated that PAH concentrations in rhizosphere soils increased with distance from the root. Results of this work provide new information on the fate of PAHs in rhizosphere.  相似文献   

19.

Purpose

A multi-compartment monitoring study was performed to characterize the effect of environmental variables, such as temperature and water flow as well as sediment characteristics, on the distribution and transport of persistent organic pollutants (POPs) in a dynamic river system during 1 year in an industrial region in central Europe.

Materials and methods

Waterborne polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were assessed over a period of 1 year at five sampling sites in the Morava River in the Czech Republic. Contaminants were measured monthly in riverbed sediments, freshly deposited sediments, water samples and passive samplers.

Results and discussion

Sediments are the main carrier of POPs in the river. Distinguishable patterns of PAHs, OCPs and PCBs in sediment indicate that their origin is from distinct sources and different transport pathways. The PAHs were identified as the dominant contaminant group of compounds with a mean concentration in sediment of 5,900 μg kg?1. Such concentrations are up to 10 times higher than in the Danube River, into which Morava drains. In contrast, mean concentrations of PCBs, hexachlorocyclohexanes (HCHs), dichlorodiphenyltrichloroethane and its breakdown products (DDTs) and hexachlorobenzene (HCB) of 6.0, 0.4, 4.2 and 6.0 μg kg1, respectively, are similar to those in the Danube. With some exceptions, no significant difference in composition of surficial riverbed sediments and those collected using sediment traps was observed. Despite the presence of potential local pollutant sources, the differences in contaminant concentrations between sites in the region were in most cases not significant. Variations in POP concentrations in sediments are mainly induced by high flow events, whereas seasonal variability was not observed.

Conclusions

The changes in contaminant concentrations in Morava River sediments are induced by episodic high flow events that cause erosion of contaminant-containing particles and their deposition at suitable downstream sites.  相似文献   

20.
Studies aimed at determining the deposition history of energy related, potentially carcinogenic, polycyclic aromatic hydrocarbons (PAHs) deposited in the sediments of Cayuga Lake, in the Finger Lakes Region of central New York State, are described. PAH fluxes in the 1850's were at least an order of magnitude less than the maximum rates in the period of 1940 to 1955. PAH fluxes began to decline before the Milliken coal fired power plant, located on Cayuga Lake, started service in 1955. Correlation between the PAH flux into the sediments and fossil fuel usage and emissions for the states of New York, Ohio and Pennsylvania and the United States as a whole, suggests that modern, high efficiency fossil fuel fired power plants are minor sources of PAHs compared to coal related residential heating and industrial combustion. Similar comparisons with historic emissions data do not support the hypothesis that PAH flux is a useful indicator of the combustion sources which produce the `acidifying' compounds SO2 and NOx for the Finger Lakes region.  相似文献   

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