Vertical Profile of PAHs and Dredging Depth of River Sediments

Sediment dredging is an effective engineering measure to reduce the negative effects of PAHs pollution on water environment. The dredging depth is a key parameter in environmental dredging engineering. A guidance of environmental dredging depth needed to reduce the toxicity risk was developed which was specifically designed for the removal of river sediments contaminated by PAHs based on the mean effect range median quotients (mean-ERM-q). The dredging depths for removing river sediments were calculated based on the vertical profile of PAHs content and the quality guidelines of sediment. Pinghu water system was carried out to determine the dredging depths of sediments from nine rivers by the proposed method. Each sediment core was collected from different river. The results showed the profiles of PAHs in sediment cores were irregular and diverse due to river dredging events and human activities in different periods. The risk assessment of PAHs toxicity showed one of nine cores with moderate-high probability, 4 of nine cores with low-moderate probability and the others with low toxicity risk. The achievement can offer a reference to the dredging engineering in other similar river systems.     

Polycyclic Aromatic Hydrocarbons (PAHs) in Surface Sediments of Lake Manzala,Egypt

This investigation represents the first extensive study of the spatial distribution, sources, and potential effects of polycyclic aromatic hydrocarbons (PAHs) in sediments from Lake Manzala, the largest of Egypt's Mediterranean coastal lakes. The concentrations of PAHs (Σ39 components) ranged from 246 to 9910 ng g^?1 dry wt., the highest values corresponding to urban hotspots with high anthropogenic input coming from wastewater discharges and combustion activities and decreasing offshore. The levels of PAHs were significantly lower compared to values reported in several coastal/estuarine areas (e.g., in Spain, Italy, USA, and Egypt) receiving substantial anthropogenic inputs from urban and industrial activities. Source ratios indicated that the PAHs were mainly from petrogenic sources in near-shore urban hotspots, with higher contributions of pyrolytic sources in coastal and offshore areas which are little influenced by human activities. Sediment quality guidelines (SQGs) showed that except at one station heavily impacted by sewage discharge, the total and individual PAH concentrations were below effect range low (ERL) concentrations that are not likely to adversely affect benthic biota.     

Norfloxacin Sorption to Different Fractions in Sediments from Typical Water Systems in China

Sorption isotherms of Norfloxacin (NOF) to different fractions from six typical sediments in China were determined to compare the NOF sorption behavior and contribution of different fractions to total sorption. All sorption isotherms were nonlinear and fitted well with the Freundlich model. Sorption coefficients (K _f) by original sediments changed in larger magnitude, from 114 (mg/g)/(mg/L)ⁿ to 5271 (mg/g)/(mg/L)ⁿ, and black carbon with more aromatic carbon has more sorption capacity and nonlinearity. The sorption capacity K _f values were found to significantly correlate with SSA (specific surface area), OC (organic carbon), BC (black carbon), and TON (total organic nitrogen) (p < 0.05), but had no obvious relation with pH, CEC (cation exchange capacity), TOC/TON, and BC/TOC. The DOC removed, NaOH extracted, and 375°C heated fractions showed more nonlinear sorption than the original sediments, suggesting more heterogeneous sorption sites in these fractions. Among different sediment fractions, the 375°C heating fractions were responsible for >50% of the total NOF sorption over the whole concentration range. The contribution of DOC removed fractions to the total sorption was the highest at higher NOF concentration.     

Influence of the Interactions Between Black Carbon and Soil Constituents on the Sorption of Pyrene

Biochar (a kind of black carbon (BC)) has been advocated as a promising additive to farmland, thus it is crucial to understand the influence of BC on the fate of hydrophobic organic chemicals (HOCs) when they exist in soil. This study explored the sorption of pyrene onto a BC sample obtained by pyrolyzing pine sawdust, two soils, clay (kaolinite), and the mixtures thereof to investigate the influence of the interactions between BC and soil constituents on the sorption of HOCs and the mechanisms therein. Sorption of pyrene onto soil?BC mixtures was significantly less than that predicted by the sum of the individual soil and BC sorption, indicating that the sorption of pyrene onto soil and BC did not occur independently. The reduction of BC sorption capacity in soil seemed primarily to be caused by soil dissolved organic matter (DOM), which attenuated pyrene sorption onto BC by 18.7%?40.3% (within pyrene equilibrium concentration range of 0.05?0.5 S _w). These were likely due to the blockage of micropores, reduced accessibility of sorption sites, and binding of pyrene by DOM in aqueous solution. In addition to the DOM effect, kaolinite also diminished pyrene sorption onto BC to some extent, which suggested additional interaction between BC and soil particles. Pyrene sorption onto the soil?BC mixtures varied with water content and contact time. The influence of wet versus dry conditions and contact time on the K_oc of pyrene was more obvious when pyrene equilibrium concentrations were lower. The effect of aging also varied with soil properties. In summary, BC could not behave independently in soil, and its sorption capacity was changed by its interactions with soil constituents, which may be influenced by soil properties, environmental condition, and contact time.     

The Contribution of Crab Burrow Excavation to Carbon Availability in Surficial Salt-marsh Sediments

Geomorphology, vegetation and tidal fluxes are usually identified as the factors introducing variation in the flushing of particulate organic matter (POM) from tidal marshes to adjacent waters. Such variables may, however, be insufficient to explain export characteristics in marshes inhabited by ecosystem engineers that can alter the quantity and quality of POM on the marsh surface that is subject to tidal flushing. In this study we evaluated the balance between transfer of buried sedimentary organic carbon (C) to the marsh surface due to crab excavation (measured from the mounds of sediment excavated from burrows) and outputs of C from the surface due to sediment deposition within crab burrows (estimated from sediment deposited within PVC burrow mimics), in a Southwestern Atlantic salt marsh supporting dense (approximately 70 ind m⁻²) populations of the crab Chasmagnathus granulatus. C excavation by crabs was much greater than deposition of C within crab burrow mimics. Per area unit estimates of the balance between these two processes indicated that crabs excavated 5.98 g m⁻² d⁻¹ and 4.80 mg m⁻² d⁻¹ of total and readily (10 d) labile C, respectively. However, sediments excavated by crabs showed a significantly lower content of both total and readily-labile C than sediment collected in burrow mimics. This indicates that ecosystem engineering by burrowing crabs causes a net decrease in the concentration of C in the superficial sediment layers and, thus, an overall decrease in the amount of C that can be washed out of the marsh by tidal action. Incorporating the in situ activities of ecosystem engineers in models of marsh export should enhance understanding of the function of marshes in estuarine ecosystems.     

土壤和沉积物中多环芳烃的界面吸附研究进展

综述了环境中多环芳烃的危害、来源及分布,并在此基础上重点介绍了多环芳烃在土壤和沉积物中界面作用的常见作用模式,包括线性分配模型和非线性吸附模型及其应用;多环芳烃疏水性有机物吸附的影响因素,主要有土壤和沉积物中含碳物质的结构类型以及多环芳烃本身的分子特性。最后提出本领域研究中的建议与展望。     

Polycyclic Aromatic Hydrocarbons in Sediments: An Overview of Risk-Related Issues

This series of articles address site-specific issues associated with evaluating exposure and toxicity of polycyclic aromatic hydrocarbons (PAHs) in sediments. These include factors that influence the opportunity to come into contact with PAHs in sediments (bioaccessibility) and those that affect the potential for transfer from sediment to ecological and human receptors (bioavailability). Although organic carbon is viewed as an important matrix for sorbing PAHs, studies have shown that there are various forms of carbon, some of which are highly sorptive. These latter forms vary on a site-specific basis and including this form of carbon in the assessment can reduce the uncertainty associated with estimating exposure. Other site-specific factors associated with water clarity, depth, and light penetration can result in enhanced toxicity of PAHs as a result of photoactivation. Chemical analyses of sediments increasingly include the alkylated PAH compounds. Although analyses of this suite of PAH compounds is being conducted to support ecological assessments and forensic analyses, there is little guidance on how to interpret the alkylated PAHs with respect to human health risks. An approach for accomplishing this is suggested.     

Sources of Lipids in Anoxic Lacustrine Sediments Using Stable Carbon Isotopes

The origin of organic matter in recent anoxic sediments of the alpine Lake Bled (NW Slovenia) was determined by analyzing the carbon isotope composition of lipid biomarkers, i.e. alkanes, alcohols, sterols and fatty acids, busing compound specific, carbon isotope analysis. The results indicate that, although biomarker analysis indicated mostly plankton and terrestrial sources for lipids, an important part of sedimentary lipids, especially sterols, are autochthonous, of anaerobic microbial (methanotrophic) origin. Marked differences were observed in δ¹³C values of lipid biomarkers in settling particles collected 2 m above the bottom, and in δ¹³C values determined in surface sediment. These results indicate that even some compounds found in both particulate organic matter and sediments are the same in terms of chemical structures, their sources can be different and thus, isotopic composition should be used as a complementary tool for source identification.     

Organic Carbon Degradation in Anoxic Organic-Rich Shelf Sediments: Biogeochemical Rates and Microbial Abundance

Identifying and explaining bottlenecks in organic carbon mineralization and the persistence of organic matter in marine sediments remain challenging. This study aims to illuminate the process of carbon flow between microorganisms involved in the sedimentary microbial food chain in anoxic, organic-rich sediments of the central Namibian upwelling system, using biogeochemical rate measurements and abundances of Bacteroidetes, Gammaproteobacteria, and sulfate-reducing bacteria at two sampling stations. Sulfate reduction rates decreased by three orders of magnitude in the top 20 cm at one sampling station (280 nmol cm^?3 d^?1 – 0.1 nmol cm^?3 d^?1) and by a factor of 7 at the second station (65 nmol cm^?3 d^?1 – 9.6 nmol cm^?3 d^?1). However, rates of enzymatic hydrolysis decreased by less than a factor of three at both sampling stations for the polysaccharides laminarin (23 nmol cm^?3 d^?1– 8 nmol cm^?3 d^?1 and 22 nmol cm^?3 d^?1– 10 nmol cm^?3 d^?1) and pullulan (11 nmol cm^?3 d^?1– 4 nmol cm^?3 d^?1 and 8 nmol cm^?3 d^?1– 6 nmol cm^?3 d^?1). Increasing imbalance between carbon turnover by hydrolysis and terminal oxidation with depth, the steep decrease in cell specific activity of sulfate reducing bacteria with depth, low concentrations of volatile fatty acids (less than 15 μM), and persistence of dissolved organic carbon, suggest decreasing bioavailability and substrate limitation with depth.     

微生物降解多环芳烃(PAHs)的研究进展

从多环芳烃(PAHs)的降解菌株的筛选、降解机制以及PAHs污染的生物修复等方面介绍了微生物降解PAHs的最新研究进展。     

Sources of PAHs to Sediments of the Elizabeth River,VA

Sediments collected from the Elizabeth River, VA, a highly contaminated subestu-ary of the James River, were analyzed for polycyclic aromatic hydrocarbons (PAHs). Select isomer ratios (BbF/BkF, BaA/chrysene, and IP/BghiP) and molecular weight fractions (ΣPAH_202/202-276 and ΣPAH_252/202-276) were identified as source indicators for two former wood-treatment facilities (Atlantic Wood and Eppinger & Russell) located on the southern branch of the Elizabeth River. These facilities are suspected as probable contributors to the high PAH contamination in sediments. Plots of the wood-treatment source indicators, along with those for coal, wood, and automotives, revealed a likely contribution from only one of the former wood-treatment facilities, in addition to the possible contribution of coal/coal gasification to PAH contamination in sediments of the main stem and southern branch of the Elizabeth River. By examining PAH isomer ratios from known or suspected sources, it is possible to distinguish multiple sources of PAHs to an ecosystem.     

Effects of carbon substrate enrichment and DOC concentration on biodegradation of PAHs in soil

AIMS: Two common reasons to explain slow environmental biodegradation of polycyclic aromatic hydrocarbons (PAHs), namely lack of appropriate carbon sources for microbial growth and limited bioavailability of PAHs, were tested in a laboratory bioassay using a creosote-contaminated soil. METHODS AND RESULTS: The soil, containing a total of 8 mg g-1 of 16 PAHs, was sieved and incubated in bottles for 45 days. The first explanation was tested by enrichment with the analogue anthracene and the non-analogue myristic acid, and both failed to stimulate degradation of all PAHs except anthracene. The second explanation was tested by addition of different concentrations of dissolved organic carbon (DOC), with effects depending on the DOC concentration and the molecular size of the PAH. The degradation was enhanced from 10 to 35% for 12 PAHs when the soil was saturated. The degraded amounts of individual PAHs were proportional to their concentration in the soil. CONCLUSIONS: The slow in situ degradation of PAHs was enhanced by more than three times by adding water as a solvent. Addition of DOC facilitated the degradation of four- to six-ring PAHs. SIGNIFICANCE AND IMPACT OF STUDY: Bioremediation of PAH-contaminated sites may be facilitated by creating water-saturated conditions but retarded by addition of other carbon substrates, such as analogue compounds.     

Importance of Environmental Black Carbon to Dissolved Petroleum Hydrocarbons Sorption on Soil

Importance of environmental black carbon (BC) to sorption of dissolved petroleum hydrocarbons (DPH) on two soils with high BC:TOC ratios (33% and 11%, respectively) was evaluated at a relatively high concentrations (mg/L ～ μ g/L range). Sorption isotherms of DPH were determined for the two original soils and soils combusted at 375°C (only BC). The sorption isotherms of the original soils were linear, whereas the isotherms of the combusted soils were highly nonlinear (n _F = 0.45, 0.60). It is indicated that intrinsic BC-water sorption coefficient is not possible to be used to estimate total sorption to the original soil, even in our relatively high concentrations. From the sorption isotherms, Freundlich coefficient of environmental BC sorption, K _F,BC ^env of 10 ^{2.55 ± 0.21} was calculated and could be used as a generic starting point for environmental modeling purposes. From the data, it could be deduced that BC was responsible for 50% of the total sorption at concentrations of 45 and 4 μ g/L (μ g/L range), which were significantly higher than literature concentrations (ng/L range). These results demonstrate that in soil with high BC:TOC ratio BC is the most important geosorbent constituent with respect to sorption of DPH at relatively high concentrations ranged in μ g/L.     

Heavy Metals (Cd,Cu, Ni,Pb, and Zn) Fractionation in River Sediments,Hamedan, Western Iran

Five heavy metals (Cd, Cu, Ni, Pb, and Zn) in river sediments from Abshineh River, Hamedan, western Iran, were fractionated by a sequential extraction procedure. Cu, Ni, Pb, and Zn existed in sediments mainly in residual fraction (mean 92%, 86%, 77%, and 65%, respectively), whereas Cd occurred mostly as organic matter (mean 41%) and exchangeable (mean 25%) fractions. The mean percent of mobile fraction of Cd, Cu, Ni, Pb, and Zn in contaminated sediments was 25, 13, 4, 24, and 10, respectively, which suggests that the mobility and bioavailability of the five metals in sediments probably decline in the following order: Cd = Pb > Cu > Zn > Ni. The metal levels were also evaluated according to the contamination factor, which revealed significant anthropogenic pollution of Cd and Pb.     

Distribution of nutrients,trace elements,PAHs and radionuclides in sediment cores from Lake Varese (N. Italy)

Sediment cores were collected at 5 stations in Lake Varese. They were analyzed for organic matter, N, P, organic C, Cd, Cr, Cu, Hg, Pb, Zn and PAHs. A sedimentological approach has been applied to estimate the ecological risk from identified pollutants.As in other eutrophic lakes in Northern Italy, this lake is also at considerable risk from heavy metal pollution. Cr, Cu and Cd showed the highest enrichment factors for the last 5 years, 23.4, 8.0 and 7.6 respectively. Other metals had enrichment factors ranging from 1 to 3. Fluoranthene was chosen as a representative PAH, derived from combustion products; its average value in surficial sediments ranged from 100 to 220 ng l^-1 dw. This compound can be a hazard to human health and aquatic life. An evaluation of radionuclide distributions after the recent Chernobyl accident in the USSR (¹³⁴Cs, ¹³⁷C s, ¹³¹I, ¹⁰⁶Ru) provided useful tracers to follow the cycling of pollutants bound to particulate matter in the aquatic ecosystem.     

Effects of Surface-Modified Nano-Scale Carbon Black on Cu and Zn Fractionations in Contaminated Soil

Cu contamination soil (547 mg kg^–1) was mixed separately with the surface-modified nano-scale carbon black (MCB) and placed in the ratios (w/w) of 0, 1%, 3%, and 5% in pots, together with 0.33 g KH₂PO₄and 0.35 g urea/pot. Each pot contained 20 ryegrass seedlings (Lolium multiflorum). Greenhouse cultivation experiments were conducted to examine the effect of the MCB on Cu and Zn fractionations in soil, accumulation in shoot and growth of ryegrass. The results showed that the biomass of ryegrass shoot and root increased with the increasing of MCB adding amount (p < 0.05). The Cu and Zn accumulation in ryegrass shoot and the concentrations of DTPA extractable Cu and Zn in soil were significantly decreased with the increasing of MCB adding amount (p < 0.05). The metal contents of exchangeable and bound to carbonates (EC-Cu or EC-Zn) in the treatments with MCB were generally lower than those without MCB, and decreased with the increasing of MCB adding amount (p < 0.05). There was a positive linear correlation between the Cu and Zn accumulation in ryegrass shoot and the EC-Cu and EC-Zn in soil. The present results indicated the MCB could be applied for the remediation the soils polluted by Cu and Zn.     

Source apportionment and risk assessment of PAHs in Brisbane River sediment,Australia

Sediment samples collected over a 3-year period from Brisbane River, Australia, were analysed for fifteen (15) polycyclic aromatic hydrocarbons (PAHs). The total PAH concentrations varied from 148 to 3079 ng/g with a mean concentration of 849 ± 646 ng/g. The study revealed that PAH input into the river was primarily dominated by pyrogenic sources as evidenced by the predominance of the high molecular weight (HMW) PAHs. Temporal variations of PAHs can be linked to the level of urbanization, with continuous input of combustion related PAHs in the commercial area of the river. Inherent deficiencies in using a single source identification/apportionment approach were overcome by using diagnostic ratios, principal component analysis/absolute principal component scores (PCA/APCS) and positive matrix factorization (PMF). Both, PCA/APCS and PMF resolved four (4) identical factors or sources of PAHs, namely: gasoline emissions, diesel emissions, biomass burning and natural gas combustion. Diagnostic ratios, PCA/APCS and PMF analysis indicated that vehicular emissions were the principal sources especially within the lower section of the river while biomass burning had moderate contribution. The distribution, temporal trend and source apportionment suggest the containment of industrial-derived sources of PAHs in the river. From an ecological point of view, the risk posed by PAHs in the Brisbane River sediment appears to be low. Nevertheless, when the investigated sites were ranked using multi-criteria decision making methods(MCDM) the commercial stratum was the most contaminated. Assessment of potential risks posed by incidental dermal exposure to PAHs revealed some degree of cancer risk, especially to children.     

Risk assessment of polycyclic aromatic hydrocarbons (PAHs) in sediments from a mixed-use reservoir

Although reservoirs in China are of great significance, very few studies on risk assessment have been reported for reservoirs. This study investigated distribution characteristics, cancer and ecological risks, and source diagnosis of 16 priority polycyclic aromatic hydrocarbons (PAHs) in sediments from Shitou Koumen Reservoir in Jilin Province, China. A total of 12 sediment samples were collected from the reservoir in August (wet season) 2014. Total PAH concentrations in sediment samples ranged from 1294.51 ng/g to 2755.35 ng/g with a mean concentration of 1757.54 ng/g. For individual PAHs, average concentration of Nap was the highest, 800.56 ng/g, while Acy, Fla, BkF, and DahA were undetected in sediment samples. Light PAHs (2–3 rings) accounting for 74.21% was a dominant PAH compositional pattern. Pearson correlation analysis was carried out; results showed that total PAHs was strongly correlated with the highly enriched sedimentary PAHs, and pH was a major factor in controlling PAH distribution. Lifetime cancer risk was employed to assess cancer risk; results indicated that the fish-culturing area was exposed to cancer risk. The molecular diagnostic ratios of isomeric PAHs were applied to identify possible PAH sources; primary PAH sources were identified as oil-related activities, burning agricultural wastes, vehicular emissions, and industrial discharges.     

Evaluation of Phosphorus Species in the Bed Sediments of an Atlantic Basin: Bioavailability and Relation with Surface Active Components of the Sediment

In this study, total phosphorus (P) concentrations and P fractions in the bed sediments of the Anllóns River (NW Spain) have been examined. The Lowest Effect Level of the Ontario Sediment Quality Guidelines was trespassed for total phosphorus (600 mg kg^?1) at three out of the five sampling sites which, in addition, showed an average of 43% of bioavailable phosphate. The inorganic P fractions (loosely bound P, redox-sensitive P, metal oxide-bound P, carbonate and apatite P, and residual P) showed that inorganic P was mostly found as metal oxide bound P. The difference between total phosphorus and the sum of the inorganic P forms determined in these extracts is attributed to P associated to organic compounds being solubilized in some of the extractants, and represented in average 58% of total phosphorus. With the exception of loosely bound P, all the P fractions showed significant positive correlations with each other and with total phosphorus.     

Role of Organic Carbon Sources and Sulfate in Controlling Net Methylmercury Production in Riverbank Sediments of the South River,VA (USA)

Mercury (Hg) transport and methylmercury (MeHg) production in riverbank sediments are complex processes influenced by site-specific physical and biogeochemical conditions. The South River watershed in VA, USA, contains elevated concentrations of Hg in riverbank and floodplain sediments, which has the potential to methylate. The role of specific organic carbon sources in promoting methylation reactions in natural sediments under dynamic flow conditions is not well understood. Four saturated column experiments were conducted, including a control column, which received South River water as an influent solution, and three columns that received South River water amended with: acetate (5.8 mM); lactate (5.7 mM); and lactate (5.7 mM) with SO₄^2? (10.1 mM). The amendments were selected to promote growth of different microorganisms to gain an understanding of the microbial processes, controlling rates of methylation. The column receiving lactate and SO₄^2? had the highest MeHg concentrations in the effluent and in the pore water near the effluent at 1.8 and 4.9 μg L^?1, respectively. At the cessation of the column experiments, the lactate–sulfate column sediments contained the highest populations of enumerable sulfur-reducing bacteria and the highest solid-phase MeHg at 530 ± 100 ng g^?1 dry wt. from the interval closest to the influent. The results suggest that the form and availability of electron donors and acceptors are primary factors controlling rates of methylation in the South River sediment.