Seasonal AVS–SEM relationship in sediments and potential bioavailability of metals in industrialized estuary, southeastern Brazil

In anoxic sediments, as those found in estuaries, the mobility of metals can be controlled by the formation of stable sulfide complexes. The potential bioavailability of a metal can then be predicted on the basis of the acid volatile sulfide (AVS) and simultaneously extracted metals (SEM) criterion. Distributions of AVS and SEM (Hg, Cu, Pb, Cd, Zn, and Ni) along the sediment profiles were determined seasonally for three rivers that constitute the Santos-Cubat?o estuarine system (SE Brazil), which is located in one of the most industrialized areas of Latin America. AVS and SEM concentrations varied significantly, from 0.04 to 31.9 μmol g⁻¹ and 0.086–6.659 μmol g⁻¹, respectively. The highest AVS levels in sediments were detected in the winter, whereas high SEM values predominated in the summer. Considering SEM–AVS molar differences as a parameter to evaluate potential bioavailability, sediments nearest to the industrial area represent higher risk to biota, especially during the summer. It is due to relatively low AVS values and not necessarily high concentrations of metals.     

Heavy metals associated with reduced sulfur in sediments from different deposition environments in the Pearl River estuary, China

Distribution of acid volatile sulfur (AVS) and the simultaneously extracted metals (SEM: Cu, Pb, Zn, Cd, Ni) in sediment profiles has been studied at five sites in Pearl River estuary, China. Of the five sampling locations, Nos.1 and 2 are in the middle shoal, Nos.3 and 4 in the west shoal and No. 5 locates to the south of the estuary. The AVS content in the sediments of the middle shoal varies in a small range (0.25–4.06 μmol g⁻¹), while that of west shoal increases with depth from 0 to ultimately 26.09 μmol g⁻¹. The SEM concentration in the sediment profiles at location Nos. 1, 2 and 5 is generally in the range of 0.95±0.2 μmol g⁻¹ with a slight upward increase, while that in the sediment of west shallows are much higher (1.43–2.42 μmol g⁻¹) with a significant upward increase, especially in the upper layer of ca. 15 cm. The observed upward increase of SEM content at all the sites implies that heavy metal contamination of sediment in the Pearl River estuary is increasing. Calculations of the excess heavy metal content which is defined by SEM-AVS molar difference suggests that the upper sediment in the Pearl River estuary, especially on the west shallows, could be a source of heavy metal contaminants and may cause toxicity to the benthos. The site-specific distribution patterns in the AVS and SEM profiles were interpreted according to the hydrogeochemistry of deposition environments.     

Historical trends of organochlorine pesticides (OCPs) recorded in sediments across the Tibetan Plateau

Sediment cores from four lakes across the Tibetan Plateau were used as natural archives to study the time trends of organochlorine pesticides (OCPs). The total concentrations of dichlorodiphenyltrichloroethane (ΣDDT) and hexachlorocyclohexane isomers (ΣHCH) were in the range of 0.04–1.61 and 0.08–1.88 ng/g based on dry weight (dw), while the input fluxes were in the range of 0.3–236 and 0.7–295 pg/cm²/y in the core sediments, respectively. The input fluxes of ΣDDT and ΣHCH generally peaked in sediment layers corresponding to the 1970s–1990s and peaked in top sediment layers. The ratio of α/γ-HCH decreased in the top layer sediments, implying that the contribution of lindane (pure γ-HCH) has been increasing in recent years. In addition, the ratio of o,p′-DDT/p,p′-DDT increased significantly over the last 15–20 years, suggesting that dicofol (characterized by high ratio of o,p′-DDT/p,p′-DDT about 7.0) has recently become a relatively more important source of DDT compared to technical DDT itself. The time trends of OCPs recorded in lake sediments examined the impact on such remote alpine regions by human activities.     

官厅水库-永定河沉积物中AVS-SEM的分析

酸可挥发性硫化物(AVS)与同步提取的重金属(SEM)之间的比例关系是控制缺氧性沉积物中重金属生物有效性及毒性的主要因素．本文设计了一套新型吹气．吸收装置测定水体沉积物中的AVS，提高了AVS的回收率及测定操作的稳定性．并应用此装置测定了官厅水库-永定河水体沉积物中AVS-SEM的分布。     

Seasonal and spatial variations of acid-volatile sulphide and simultaneously extracted metals in the Yangtze River Estuary

Surface sediments were collected from the Yangtze River Estuary (YRE) in May 2012, August 2012, November 2012 and February 2013 to analyse the seasonal and spatial distributions of acid-volatile sulphide (AVS), simultaneously extracted metals (SEM) and the sediment toxicity. An optimised method was used for the AVS and SEM analysis and the results showed that the seasonal variations of AVS were positively correlated with changes in water temperature and the position of higher AVS was relatively fixed. The average of SEM was gradually increased from May 2012 to February 2013 and there were abnormally high values of SEM_Cu and SEM_Ni in the YRE. Concentrations of the five SEM components were in the following order: Cd?相似文献   

Aliphatic and polycyclic aromatic hydrocarbons in the bottom sediments from Klaipėda Harbour,Lithuania (Baltic Sea)

A total of 22 bottom surface sediment samples were collected from Klaip?da Harbour, Lithuania (Baltic Sea). Sediment parameters, such as grain size and concentrations of total organic carbon, aliphatic hydrocarbons (ALHs) and polycyclic aromatic hydrocarbons (PAHs), were determined. Hydrocarbon contamination levels in the sediments were estimated based on classifications provided in the literature, and potential biological effects were assessed based on the effects range low–effects range median values of the Sediment Quality Guidelines and on the total toxic benzo(a)pyrene equivalent. The results demonstrated that concentrations of PAHs and total aliphatic hydrocarbons in the sediments varied between 1.6 and 5456?ng?g^?1 d.w. and 6.9 and 727?μg?g^?1 d.w., respectively. In most cases, the concentrations of ALHs and PAHs in the sediments indicated low to moderate levels of pollution and were not observed to have any significant adverse effects on living biota. To determine possible sources of hydrocarbons, hydrocarbon compositions were analysed, and ALHs’ and PAHs’ specific diagnostic ratios were calculated. According to the results, the Klaip?da Harbour bottom sediments were dominated by PAHs of pyrogenic origin, whereas the origin of ALHs was mixed, that is, anthropogenic with a biogenic (aquatic and terrestrial) input.     

Polycyclic aromatic hydrocarbons in medicinal plants from Syria

The levels of 16 US Environmental Protection Agency polycyclic aromatic hydrocarbons (EPA PAHs) in 10 medicinal plants in different used parts of plant (leaves and flowers) have been determined. The analytical method consists of sample preparation by ultrasonic extraction with dichloromethane followed by silica gel clean-up. Subsequently, the analysis was carried out by reversed-phase high-performance liquid chromatography (HPLC) coupled to both ultraviolet and fluorescence detections in series to insure the detection of all 16 EPA PAHs. It was observed that the sum of the 16 PAHs (ΣPAHs) in the investigated medicinal plants ranged from 47 to 890 μg kg^–1 where the highest ΣPAHs was found in Sage plant sample. Light PAHs were dominants in all studied medicinal plants. The sum of eight genotoxic PAHs (ΣPAH8) have shown a better indicator of the degree of contamination with carcinogenic PAHs compared to benzo[a]pyrene in these products.     

Organochlorine pesticide residues in fodder from rural areas of Haryana,India

Residues of organochlorine pesticides (OCPs) namely 1,2,3,4,5,6-hexachlorocyclohexane isomers (HCH-isomers), 1,1,1-trichloro-2,2-bis(p-chlorophenyl) ethane (DDT) and its metabolites, and endosulfan stereoisomers were analyzed in dry and green fodder samples from rural areas of Ambala, Gurgaon, and Hisar districts of Haryana, India during winter, summer, and post-monsoon seasons. The HCH isomers γ-HCH and β-HCH, and DDT and its metabolites p,p′-DDD, p,p′-DDE, and p,p′-DDT had more traceability in test samples as compared to other isomers and metabolites studied. Total OCPs (ΣOCPs), i.e., ΣHCH, ΣDDT, and Σendosulfan were found to be the highest in wheat straw (1.1–1.2?mg?kg^?1) from Ambala and Gurgaon, followed by that in sorghum straw (0.46?mg?kg^?1) from Hisar. Dry fodder samples were found to have relatively higher residue levels than green fodders. In case of green fodder samples, maximum ΣOCP residues of 0.44?mg?kg^?1 were found in whole plant samples of sorghum from Gurgaon district followed by that in pearl millet (0.40?mg?kg^?1) from Ambala. The findings indicate highly significant differences (p?>?0.0001) in ΣOCPs and ΣDDT in wheat straw between different districts and reveal the persistence of OCP residues in both dry and green fodder samples in the study area.     

Vorschlag zur Auswertung von PAK-Kontaminationen

The behaviour of this group of substances may be considered as an example for the ubiquitous occurence of xenobiotics in the environment. Regrettably, the measurements presented in numerous publications often cannot be directly compared with each other. A first step towards harmonization can be achieved by referring the measuring programmes or the presentation of results to the six aromatics of the German Drinking Water Ordinance (TWV) (Σ6) or the sixteen compounds of the EPA list. The tendency of the PAH group to fractionation in air, water, and soil as well as in some cases during analysis must be taken into acount. In this respect, the first six aromatics of the EPA list are only partially suitable for comparisons of results. The six TWV aromatics in soils, sediments, aquatic suspended solids, and sewage sludges, and to a certain extent also in airborne dust, make up a mass portion of C_Σ6=40–50% of the Σ16 according to EPA. For Fluoranthene (Fluo) and Benzo(a)pyrene (Bap) as quide parameters, concentration quotients [single aromatic versus (Σ6)] may be given as estimates, which are on average C_Fluo=33%, and C_Bap=13%. By means of these quotients it is possible to calculate the values for the whole list by means of the data of the single aromatic C_Fluo×3=C_Σ6, or C_Bap×7,7=C_Σ6, and as a check C_Fluo/C_Bap=2,5. For estimating purposes, the relation between the two lists may be assumed als C_Σ6×2=C_Σ16. These estimating values apply to mixes of PAH, which originate from many single sources (emitters), are transported through the atmosphere with dust and settle, and/or enter water bodies after being washed from road surfaces. The estimates serve as plausibility check and for extrapolation, but they cannot replace the analysis for individual substances in the identification of the pollution source or in the study of their environmental behaviour.     

Historical record of anthropogenic polycyclic aromatic hydrocarbons in a lake sediment from the southern Tibetan Plateau

High-altitude lake sediments can be used as natural archives to reconstruct the history of pollutants. In this work, the temporal distribution of polycyclic aromatic hydrocarbons (PAHs) was determined in a sediment core collected from the southern Tibetan Plateau (TP), which was dated by using the ²¹⁰Pb dating method and validated with the ¹³⁷Cs fallout peak. The concentrations of the anthropogenic PAHs (Σ₈PAH) in the sediment core ranged from 0.83 to 12 ng/g dw, and the fluxes of the Σ₈PAH were in the range of 2.1–27 g/cm²/year. The temporal variations in the concentration and input flux of anthropogenic PAHs were low with little variability before the 1950s, and then gradually increased from the 1950s to the 1980s, and an accelerated increase was observed after the early 1980s. The content of total organic carbon played an insignificant role in affecting the time trends of PAHs in the sediment core. Diagnostic concentration fractions of PAH components indicate PAHs in the lake sediment of the southern TP which are mainly from biomass burning and/or from long-range atmospheric transport.     

Bioavailability of a hydrocarbon from water and sediment to the marine worm Arenicola marina

The uptake, accumulation and depuration of a labelled hydrocarbon (¹⁴C-1-naphthalene) by the marine annelid Arenicola marina were studied. Naphthalene was chosen because it is an important component of oil and is known to be toxic to marine organisms. The bioavailability of the hydrocarbon to the worm from contaminated sediment is examined and the results discussed with reference to the rehabilitation of oiled environments, as A. marina is thought to be capable, in high numbers, of greatly reworking sediments.     

Accumulation of Organochlorine Compounds in Oysters (Crassostrea Gasar) of an Estuarine Environment: Case of A Tropical Lagoon in the Gulf of Guinea

As part of a pollution monitoring study, oysters (Crassostrea gasar) were sampled in June 1996, in order to determine the concentrations and distribution of chlorinated hydrocarbons in two stations (near Boulay Island and Riviera Golf) of the Ebrie Lagoon, in the Abidjan area.

The chromatographic analysis of the oven dried samples revealed the presence of PCBs (2.13 to 86.22 ppb or ng/g dry weight), DDE (<0.48 to 169.55 ppb), DDD (<1.04 to 60.27 ppb), DDT (1.43 to 77.81 ppb, lindane (<0.22 to 91.64 ppb), aldrin (<0.30 to 154.1 ppb), endrin (<0.23 to 293.31 ppb) and dieldrin (<0.26 to 199.74 ppb). the results indicated high concentrations in oysters sampled near Boulay Island, due to industrial, agricultural and port activities going on in this area.

Compared to DDD/ΣDDT and DDT/ΣDDT, the DDE/ΣDDT ratios were high indicating old DDT inputs. the ΣDDT/PCBs ratios were higher than 1 illustrated the predominance of organochlorine inputs from agriculture activities. the presence of lindane in both stations illustrated the problem of fishing with toxic products.

Negative correlations found between dry tissue weight and organochlorine compounds concentrations showed that young oysters may concentrate more of these substances. More studies are needed in order to make any conclusions on their bioaccumulation trends.     

Monitoring and risk assessment of polychlorinated biphenyls (PCBs) in agricultural soil from two industrialized areas

For monitoring and risk assessment, levels and distributions of Σ₂₉ PCBs in paddy soil samples collected from Gwangyang (10 sites) and Ulsan (20 sites), heavily industrialized cities in Korea, were investigated using high-resolution gas chromatography/high-resolution mass spectrometry. Overall, total concentrations of Σ₂₉ PCBs in Gwangyang (216.4–978.6 pg g^?1 dw) and Ulsan (273.8–1824.1 pg g^?1 dw) were higher than those (106.6–222.6 pg g^?1 dw) in agricultural soil from Anseong in Korea. The TEQ (toxic equivalency) values from Gwangyang (0.06–0.40 ng TEQ kg^?1 dw) and Ulsan (0.06–0.22 ng TEQ kg^?1 dw) were higher than those (0.04–0.11 ng TEQ kg^?1 dw) in Anseong but lower than the WHO threshold level (20 ng TEQ kg^?1). However, one of the most toxic congeners, PCB 126, gave the highest concentration, possibly posing a risk to the biota. Seven indicator PCB congeners contributed to 50–80% of the total concentration of Σ₂₉ PCBs, indicating the 7 PCBs can be used as valuable indicators for monitoring. The principal component analysis and cluster analysis for the homologue profiles of PCBs indicated that all the samples from both cities had the similar PCB contamination patterns, and the major sources of the PCB contamination were most likely from the usage of Aroclor 1254 than those of Aroclors 1242 and 1260. These PCB technical mixtures were possibly significantly used by various industries including iron and steel industries in Gwangyang and petrochemical and shipbuilding industries in Ulsan.     

Nuclear magnetic resonance studies of interactions between organic pollutants and soil components,a review

This article presents a short overview of selected recent papers using nuclear magnetic resonance (NMR) to investigate interactions between organic pollutants and soil components such as organic matter, clays, whole soils, and sediments. First, we describe solid state cross polarisation magic angle spinning (CP-MAS) experiments as the main tools to investigate covalent bonds. Second, we report NMR approaches allowing us to assess molecule mobility and to characterise non-covalent interactions. Those approaches include correlations between K _oc values and soil organic matter functions determined by CP-MAS, ²H NMR fingerprints, relaxation time measurements, ¹⁹F and ¹H high resolution (HR)-MAS experiments.     

水体和沉积物中毒害污染物的生态风险评价方法体系研究进展

人类活动导致大量毒害污染物进入水体和沉积物,从而对水生生物产生诸多不利影响.开展毒害污染物的生态风险评价,筛选高风险毒害污染物,是毒害污染物风险管控和生态系统保护的基础.对美国和欧盟等发达国家和地区毒害污染物的生态风险评价方法进行了综述.水体和沉积物中毒害污染物风险评价的基本方法首先是采用预测或测定环境浓度(PEC或M...     

Effect of monsoonal climate on sulfate reduction in coastal sediments of the central Great Barrier Reef lagoon

Rates of sulfate reduction were measured during the spring dry and summer wet seasons of 1992 in shallow coastal sediments of the central Great Barrier Reef lagoon. In the dry season, sulfate reduction rates, integrated to 18–20 cm depth, ranged from 23.8 to 30.8 mmol S m^-2 d^-1. In the wet season, heavy monsoonal rains and wind-induced waves caused severe disturbance of sediments leading to less anoxic conditions, and to a 2- to 3-fold decline in rates of sulfate reduction (10.2 to 12.8 mmol S m^-2 d^-1). The percentage of reduced ³⁵S recovered as acid-volatile sulfide (% AVS_red) ranged from 15.8 to 44.9% in spring, and was significantly reduced at each station in summer (range 14.5 to 31.4%). An analysis of variance indicated that seasonality accounted for 31.5% of the total variance in total rates of sulfate reduction, with only 7.5% of the variance accounted for by depth into the sediment; there were no station differences. In both seasons, there were no clear patterns in the proportion of radiolabel incorporated into the AVS and chromium-reducible sulfur (CRS) pools with depth into the sediment. These results are contrary to the seasonal patterns and pathways of sulfate reduction in temperate coastal sediments.     

Bioavailability of hydrophobic organic contaminants and quality of organic carbon

U.S. laws require that contaminant bioaccumulation potential be evaluated before dredged material can be recycled. Simple fugacity models, e.g. organic contaminant aqueous partition coefficient (K _oc)-derived theoretical bioaccumulation potential, are commonly used to estimate the partitioning of hydrophobic organic contaminants between sediment organic matter and organism lipid. K _oc-derived models, with or without the addition of a soot carbon term, did not accurately or consistently predict total polycyclic aromatic hydrocarbons (PAHs) and polychlorobiphenyls partitioning of eight sediments from ongoing dredging operations onto C₁₈-coated filter paper. These models also failed to predict the partitioning of individual PAHs from these eight sediments. These data underscore the trade-offs between the ease of using simple models and the uncertainty of predicted partitioning values.     

沉积物中重金属Pb和Cd对河蚬的毒性效应研究

以河蚬为受试生物,以存活率、呼吸抑制率为测试终点,研究了沉积物和上覆水中重金属Pb、Cd对底栖生物的毒性效应,并探讨了沉积物中酸挥发性硫化物(acid volatile sulfide,AVS)和同时提取金属(simultaneously extracted metals,SEM)对重金属生物有效性的影响。结果表明,沉积物中Pb、Cd对河蚬致死效应较低,当Pb、Cd浓度分别为400、100 mg獉kg-1,连续暴露21 d时,致死率低于20%;沉积物中Pb、Cd对河蚬14 d的呼吸抑制率EC50分别为519和151 mg獉kg-1;上覆水中Pb和Cd离子浓度较低,对生物毒性效应贡献可以忽略;SEM/AVS值和生物呼吸抑制率有着明显的线性相关性,当SEMPb/AVS1,SEMCd/AVS0.6时,重金属对河蚬有明显的毒性效应。     

Interlinked temporal changes in environmental conditions, chemical characteristics of sediments and macrofaunal assemblages in an estuarine intertidal sandflat (Seto Inland Sea, Japan)

Five field surveys were conducted in an estuarine intertidal sandflat of the Seto Inland Sea (Japan) between April 1994 and April 1995. Chlorophyll a, pheopigments, total organic carbon and acid-volatile sulphides (AVS) of surface and subsurface sediments, and macrofaunal assemblages were investigated in parallel at 15 stations. Monthly hydrological data of low-tide creek water adjacent to the flat were used as a complementary environmental characterisation of the study area. Strong temporal changes were found among sampling dates, most remarkably in autumn with a major increase of algal detritus and AVS, a sharp reduction in macrofaunal abundances and species richness, and a massive mortality of the clam Ruditapes philippinarum. This dystrophic event was preceded by a photoautotrophic and hypertrophic spring–summer characterized by abundant fresh (i.e., living) algal material, including microphytobenthos and macroalgae (Ulva sp.). In summer, abundant macrofaunal assemblages reached the highest biomass values (455 g wet weight m⁻² or 60.6 g ash free dry weight m⁻²), with a major contribution of filter-feeding bivalves Musculista senhousia and R. philippinarum. These are among the highest values reported in the literature for sedimentary shores. From autumn, there was a progressive recolonisation of macrofauna, initiated by few opportunistic polychaetes (e.g., Cirriformia tentaculata and Polydora sp.), apparently promoting a fast sediment recovery in winter, and followed by new bivalve recruits in the next spring. This study provides the first evidence of significant and interlinked within-year changes in chemical characteristics of sediments and macrofaunal assemblages in an estuarine intertidal flat at a small spatial scale (i.e., tens of meters). This demonstrates the high temporal variability of species–environment relations in these systems and a close relationship in seasonally driven trophodynamic processes among primary producers and benthic consumers. We conclude that a thorough parallel evaluation of the temporal changes in chemical characteristics of sediments should be taken into account in assessing the year-round distribution and changes of intertidal macrofauna, particularly in eutrophic, estuarine intertidal flats.An erratum to this article can be found at     

Metal partitioning in sediment pore water from the Ondo coastal region,Nigeria

Distribution and equilibrium partitioning of metals (Cd, Cu, Cr, Fe, Ni, Pb, Mn, and Zn) between pore water and surface sediments at the Ilaje coast of Ondo State, Nigeria, were studied. The Ilaje River can be one of the interesting research locations because of its economic nature and history of oil pollution. Seasonal variations were observed to investigate possible variations in the availability of metals for organisms throughout the year. The concentrations in both sediments and pore water during the dry and wet seasons were as follows: Cu?>?Fe???Mn?>?Pb?>?Ni?>?Cr?>?Cd?>?Zn. The pore water–sediment partition coefficient (K _p) showed that Zn and Cd were highly mobile while Fe and Cu have restricted mobility. Dissolved organic carbon (DOC) in pore water had a strong influence on mobility and bioavailability of all the metals (p?K _oc), increased levels of Fe and Cu were linked to lithological origin. Concentrations of Pb and Ni were associated with petroleum-related sources. The significance of the field-based techniques for ecotoxicological purposes is discussed.