Levels of estrogenic compounds in Xiamen Bay sediment, China

Concentrations of seven estrogenic compounds, i.e., estrone (E1), 17β-estradiol (E2), 17α-ethynylestradiol(EE2), diethylstilbestrol (DES), nonylphenol (NP), octylphenol (OP) and bisphenol A (BPA), were determined in sediments and pore water from Xiamen Bay in China, and their distributions and potential risks in the Bay were assessed. Total estrogenic compounds concentrations varied from 49.20 to 1230.69 ng/g dw in sediments and from 102.33 to 4376.60 ng/L in pore water. The highest levels of these compounds were found at Yundang Lagoon. The results showed that estrogenic compounds in Xiamen Bay originated mainly from municipal wastewaters. Compared with other areas, Xiamen Bay was contaminated with high levels of estrogen hormones. This contamination poses a potential threat to benthic organisms. Although a good relationship (r = 0.94) was observed between the estrogenic compounds concentrations and total organic carbon (TOC) contents in sediments, which did not indicate that the sediment organic matter favors the accumulation of the detected estrogenic compounds.     

Concentrations of organotin compounds in blue mussels from the wharves of Tokyo Bay

Organotin compounds (tributyltin (TBT), dibutyltin (DBT), monobutyltin (MBT), triphenyltin (TPT), diphenyltin (DPT), and monophenyltin (MPT)) were quantified in blue mussels, Mytilus edulis, in 1989 at 26 wharves along Tokyo Bay. Organotin compounds, other than DPT, were detected in all mussel samples (in case of DPT: 23 of 26). The concentration of DBT was highest among butyltin compounds and that of TPT was highest among phenyltin compounds. The results showed that relatively high concentrations of organotin compounds persist in blue mussels of Tokyo Bay, although the use of the paints containing these compounds has been limited for several years by regulations.     

Behaviour of hexachlorocyclohexane isomers and Zn,Cu and Cd in the freshwater-seawater mixing area

Dissolved and suspended concentrations of hexachlorocyclohexane isomers, α, γ and δ HCH, and Zn, Cu and Cd have been measured in the Napostá Grande stream, located in the Blance Bay area, Argentina, for the purpose of studying the behaviour of these compounds in the freshwater-seawater mixing zone. The aim was to establish the mobilization processes, according to their distribution over the dissolved and suspended forms, in order to obtain a better understanding of their impact on organochlorine and heavy metal levels in the marine environment. It is concluded that the compounds studied are removed from solution by suspended matter which is afterwards precipitated during the freshwater-seawater mixing process. Seawater and surface sediment concentrations of these pollutants for two sampling sites in Blanca Bay, Argentina, are also reported.     

Persistent organic pollutants and histological lesions in Mayan catfish Ariopsis assimilis from the Bay of Chetumal, Mexico

Livers of catfish (Ariopsis assimilis) from the Bay of Chetumal were analyzed for organochlorine compounds and hydrocarbons as part of a study to diagnose the environmental health of the Bay after a catfish mass mortality that occurred in 1996. The presence of histological lesions in several organs of the fish as result of chemical exposure was also evaluated. The concentrations of organic pollutants found in the Bay may be considered high if compared to the levels reported for sites affected by chemical pollution. High prevalences of cellular alteration histopathologies were found in liver, including hepatic tumors. The presence of some lesions may be related statistically to environmental pollution in the Bay, specially with chlorinated compounds.     

Impact of offsite sediment transport and toxicity on remediation of a contaminated estuarine bay

Sediment of Ostrich Bay, an arm of Dyes Inlet on Puget Sound, was historically contaminated with ordnance compounds from an onshore US Navy facility. An initial recommendation for a sediment cover to mitigate benthic risks was followed by studies of sediment transport and deposition to determine whether contaminated sediment from Dyes Inlet or other offsite sources in Puget Sound may contribute to Ostrich Bay impacts. A Sediment Trend Analysis (STA) identified net sediment transport pathways throughout the bay and inlet by examining changes in grain size distributions in multiple adjacent samples. Results indicated that fine-grained sedimentary material transports into and deposits throughout the Dyes Inlet system, with no erosion or transport out of Ostrich Bay. Echinoderm larvae mortality bioassay results were elevated in fine-grained sediments of both Ostrich Bay and Dyes Inlet. Ordnance compounds were undetected, and although sediment mercury concentrations were elevated at 0.48-1.4 mg/kg in both waterbodies, the relationship with toxicity was weak. Results of the studies and sedimentation modeling indicate that impacted sedimentary material deposits throughout the Dyes Inlet/Ostrich Bay system from unknown sources and will prevent natural recovery of Ostrich Bay as well as negate long-term effectiveness of active remedial measures. Stakeholders have recognized that remediation of the bay can be achieved only after the toxicity of depositing sediment decreases.     

Multi-residues of organic pollutants in surface sediments from littoral areas of the Yellow Sea, China

Concentrations of all studied organic pollutants, except for DDTs, were greatest at sites in Dalian Bay, where surface sediment concentrations of PHCs, PAHs, PCBs and DDTs exceeded the corresponding ERL values. The sum concentration of DDTs was greatest in Haizhou Bay exceeding the related ERM value. In terms of compositions of PAHs and PAEs, the predominant components were the MMW and HMW compounds, DBP and DEHP, respectively. The main degradation product of p,p'-DDT was p,p'-DDD at most sampling sites. The principal sources of PAHs and DDTs involved various pyrolytic processes (i.e., combustion of biomass and vehicle exhaust), and application of technical DDT (in the form of impurity or raw material), and a mixture of technical DDT and technical dicofol. Moreover, the coastal site with greatest potential ecological risk from total PAHs was located in Dalian Bay, while the littoral areas of Dalian Bay, two harbor cities (Yantai-Weihai), Jiaozhou Bay, and Haizhou Bay, had relatively high potential risk from DDTs, especially in Haizhou Bay.     

Horizontal and vertical distribution of PCBs and chlorinated pesticides in sediments from Masan Bay,Korea

Horizontal and vertical distributions of organochlorine compounds (OCs) were determined in sediments from Masan Bay. The concentrations of polychlorinated biphenyls (PCBs), dichlorodiphenyltrichloroethanes (DDTs), HCB, hexachlorocyclohexanes (HCHs) and chlordane related compounds (CHLs) in sediments were in the range of 1.24-41.4, 0.28-89.2, 0.02-0.59, nd-1.03, and nd-2.56 ng/g, respectively. The spatial distribution of OCs showed a negative gradient from the inner of the bay to outer part of the bay, indicating that the source of OCs was probably located inside the bay. Compositional pattern of PCB congeners showed a relatively high concentration of high-chlorinated congeners in the inner part of the bay and a relatively low concentration of low-chlorinated congeners in the outer part. In sediment core from Masan Bay maximum concentrations of PCBs and DDTs are observed in the subsurface samples and correspond to an age of early 1980s and late 1960s. The concentration profiles of PCBs and DDTs in sediments of Masan Bay appear to correspond to use of PCBs and DDTs in Korea.     

Distribution and sources of polynuclear aromatic hydrocarbons in Mangrove surficial sediments of Deep Bay, China

Twelve sediment samples collected from three transects of mangrove swamp of Deep Bay, Shenzhen, China, were determined for polynuclear aromatic hydrocarbons (PAHs). The total PAHs concentrations ranged from 237 to 726 ng g(-1) dry weight, and showed strong correlation with total organic carbon (TOC), clay content and Pb concentrations. The highest PAHs concentrations were found in the samples from mangrove sediments. Overall, PAHs in Deep Bay sediment were lower than those in other developed areas. The biological effect due to PAHs alone in Deep Bay is expected to be low, based on the comparisons of individual and total PAHs concentrations determined in the sediment with those in USEPA sediment quality guidelines. Four and five-ring compounds dominated the PAHs composition pattern profiles. Principal component analysis (PCA) was applied to further investigate the source of PAHs. The PAH sources of Deep Bay mangrove swamp were suggested to be primarily combustion of fossil fuel, especially leaded-gasoline exhaust.     

Occurrence of volatile organic compounds (VOCs) in Liverpool Bay, Irish Sea

Surface seawater samples were collected in the Irish Sea and Liverpool Bay area from the R.V. Prince Madog during the period of 25-31 of March 2006. VOCs were purged with nitrogen, pre-concentrated on a SPME fibre and analysed immediately on a GC-MS. Target compounds quantified were halogenated (0.2-1400 ng L(-1)), BTEXs and mono-aromatics (1.5-2900 ng L(-1)), aliphatic hydrocarbons and others (0.6-15,800 ng L(-1)). Day and night sampling was performed at a single station and suggested that factors such as sunlight and tide affect the presence of many of these compounds. Sample variability was high due to the variable weather conditions at the station. Poor correlations were found between marine phytopigments and selected VOCs. Principal component analysis (PCA) analysis showed that chlorinated compounds such as 1,2-dichloroethane, 1,1,1-trichloroethane, trichloroethene, tetrachloroethene and carbon tetrachloride, predominantly from anthropogenic sources, originated from the River Mersey. Other brominated and iodinated compounds quantified were more likely to be from biogenic sources including novel marine compounds such as 2-chloropropane, 1-bromoethane and 1-chlorobutane.     

Polycyclic aromatic and aliphatic hydrocarbons pollution at the coast of Aliağa (Turkey) ship recycling zone

Alia?a Bay is one of the most important maritime zones of Turkey where shipping activity, shipbreaking industry, steel works and petrochemical complexes exist together. Polycyclic aromatic hydrocarbons (PAHs) and aliphatic hydrocarbons in sediment of the Alia?a Bay were investigated to evaluate an environmental risk assessment from PAHs contamination in 2009-2010. Aliphatic and PAHs diagnostic ratios were showed to be mainly petroleum-originated and pyrolitic contaminations, respectively. The TEL/PEL analysis suggests that Alia?a sediments were likely to be contaminated by acutely toxic PAH compounds.     

Sources and distribution of aliphatic and polyaromatic hydrocarbons in sediments of Jiaozhou Bay, Qingdao, China

The composition and distribution of aliphatic (n-alkanes) and polyaromatic hydrocarbons (PAHs) were measured for the surface sediments collected at 25 sites from Jiaozhou Bay, Qingdao, China. Total n-alkanes and PAH concentrations ranged from 0.5 to 8.2 microg/gdw and 0.02 to 2.2 microg/gdw, respectively, and the distribution of both n-alkanes and PAHs showed large spatial variations in the bay. The distribution of PAHs in the sediments was predominated by the three or more ring compounds. High hydrocarbon levels were generally found in the areas associated with high anthropogenic impact and port activities in the bay. The calculated hydrocarbon indexes suggest that petroleum contamination was the main source of n-alkanes, while both pyrolytic and petrogenic sources contributed PAHs to the surface sediments of Jiaozhou Bay. In comparison to other polluted coastal sediments, the level of contamination from both aliphatic hydrocarbons and PAHs in Jiaozhou Bay sediments is relatively low at the present time.     

太湖梅梁湾藻华暴发消退-周期表层水体溶解性有机质分子特征

人类活动引起的富营养化对太湖的碳循环模式可能产生严重影响,精细描述太湖藻华暴发-消退周期的溶解性有机质分子是了解太湖碳库动态变化的关键.本研究利用傅立叶变换离子回旋共振质谱技术,以太湖北部梅梁湾2017年5月至2018年5月的表层水体为研究对象,解析藻华暴发-消退周期溶解性有机质的来源和分子组成特征,进而理解浮游藻类异常增殖对水体溶解性有机质的影响及其在区域碳循环中的角色.研究结果表明,藻华暴发期浮游藻类生产力显著增加,使得表层水体的溶解性有机质从含量到分子组成均发生剧烈改变.含量上表现为溶解性有机碳浓度升高,分子组成上表现为CHO类化合物和以脂肪族类化合物为代表的活性组分占比增加,特征化合物以相对高饱和度和高含氧的小质量数分子为主.而在藻华消退期,随着藻类有机质贡献的减少和有机质降解过程的持续进行,含量上表现为溶解性有机碳浓度下降,分子组成上表现为CHOS、CHONS类化合物和富羧酸脂环类化合物等惰性分子占比增加,特征化合物以大质量数分子和相对低饱和度和低含氧的小质量数分子为主.研究结果表明,太湖水体的溶解性有机质分子组成在藻华暴发期受藻类有机质输入控制,在消退期受藻类有机质降解的影响.     

The use of a spatially heterogeneous simulation model for studying biotransformation processes of nitrogen and phosphorus compounds and the dynamics of oxygen dissolved in water in the ecosystem of Neva Bay, the Gulf of Finland: 2. Input data for calculations, modeling results, and their analysis

The data collected for model calculations is systematized for natural and design conditions. The natural conditions did not take into account the effect of the complex of water-protection structures on the hydrological regime of Neva Bay and on the biogenic load onto this water area, while the design conditions, conversely, reflected the possible impact of those structures on the hydrology and ecology of the area. Numerical experiments were used to study the processes of transformation of N and P compounds and the dynamics of dissolved O₂ in Neva Bay water area. In the comparison of the calculated and observed concentrations of biogenic substances, Theil criterion was evaluated to assess the adequacy of the model in reproducing the concentration fields of the distribution of biogenic substances over Neva Bay water area. The major qualitative and quantitative features of the formation of the spatial heterogeneity and the time variations in the concentrations of biogenic element compounds over Neva Bay water area are identified. Possible improvements of the model in the reproduction of the complex of processes that are of particular importance for the development of substance transformations in shallow ecosystems are considered.     

Distribution and sources of organochlorinated contaminants in sediments from Izmir Bay (Eastern Aegean Sea)

Eighteen surface sediment samples representative of the entire Izmir Bay were analyzed for organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs). This was in order to provide extensive information concerning the recent deposition of these compounds in this area, together with levels, distribution, possible sources and potential biological risk. Sites that were contaminated by high concentrations of organochlorine compounds were associated with dense population, such as the harbour and the Gediz River estuary. Relatively higher ΣDDT concentrations and high DDT/DDE + DDD ratios in the Gediz River estuary indicated DDT usage, probably linked to public health emergencies. According to the established guidelines for sediment quality, the risk of adverse biological effects from such levels of OCPs and PCBs as recorded at most of the study sites was insignificant. But the higher concentrations in Inner bay and in the Gediz River estuary could cause biological damage.     

Screening level ecological risk assessment for synthetic musks in surface water of Lake Taihu, China

A total of thirty-three surface water samples were collected from Meiliang Bay, Gonghu Bay and Xukou Bay of Lake Taihu, and analyzed for synthetic musks, including 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-[γ]-2-benzopyrane (HHCB), 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene (AHTN), 1-tert-butyl-3,5-dimethyl-2,5-dinitro-4-acetylbenzene (MK) and 1-tert-butyl-3,5-dimethyl-2,4,6-trinitrobenzene (MX). Ecological risks of these compounds were characterized by hazard quotient (HQ) method due to a lack of sufficient available toxicity data of synthetic musks. HHCB was the main synthetic musk detected in Lake Taihu, followed by AHTN, MK, and MX. The risk assessment results indicate that low ecological risks were posed by HHCB and total synthetic musks, and even lower risks posed by other synthetic musks in the worst case; much lower ecological risks were caused by both individual and total synthetic musks in the general case. The combined ecological risk from total synthetic musks calculation suggests that the combined ecological risk from all four synthetic musks was expected to be slightly higher than for the individual musks due to their joint action. The HQ spatial distribution maps show that several hot-spot areas were mainly around the river inlets to Lake Taihu, indicating that synthetic musks may be transported to Lake Taihu with municipal sewage and industrial wastewater from surrounding areas. However, the ecological risks in hot-spot areas posed by individual and total synthetic musks were still acceptable.     

Accumulation of Butyltins in Sediments and Lipid Tissues of the Asian Clam,Potamocorbula amurensis,Near Mare Island Naval Shipyard,San Francisco Bay

Studies of butyltin compounds in soil, benthic sediments and the Asian clam Potamocorbula amurensis were conducted at the former Mare Island Naval Shipyard, and nearby Mare Island and Carquinez Straits in San Francisco Bay, California. Soils from a sandblast abrasives dump site at the shipyard contained low concentrations of mono-, di- and tributyltin (0.3–52 ng/g, total butyltin). Similarly, concentrations of total butyltin in benthic sediments from nearby Mare Island and Carquinez Straits ranged from 1.3 to 8.1 ng/g. In contrast, clams accumulated much greater concentrations (152–307 ng/g, total butyltin). Tributyltin (TBT) and dibutyltin (DBT) made up from 54–85% to 15–46%, respectively, of the total butyltin body burden of the clams. Biota Sediment Accumulation Factors (BSAFs) for butyltins in Potamocorbula were in reasonable agreement with literature values; they are greater than those of neutral hydrophobic compounds, suggesting that partitioning and binding processes may be involved in bioaccumulation. Tributyltin is a potent endocrine disrupting chemical. There is potential for long-term chronic effects of TBT in San Francisco Bay.     

Biotransformation of Organogenic Substances in the Aniva Bay Waters: Assessment with the Use of Mathematical Modeling

Mathematical modeling is used to study the conditions of natural biotransformation of biogenic element compounds (containing C, N, P, Si) in five areas within Aniva Bay. The input data for the model are evaluated with the use of GIS “Sakhalin Shelf” and the available reference literature on the bay oceanography. Water masses that transferred through the boundaries between the areas were evaluated based on the values of water level, river runoff, atmospheric precipitation, evaporation, and the volume of water in the bay, all of which vary as a result of water heating. The model was used to evaluate annual variations in the concentrations of organic and mineral fractions of these elements and the biomasses of planktonic organisms for the five areas in the bay. Modeling results also allowed the assessment of biogenic substance input with river runoff into Lososei Bay. Based on the internal fluxes of substances, the monthly and annual aquatic animal production was evaluated.     

Concentrations of methyl- tert-butyl ether (MTBE) in inputs and receiving waters of Southern California.

The occurrence and concentration of the fuel additive methyl-tert-butyl ether (MTBE) were measured in dry weather runoff, municipal wastewater and industrial effluents, and coastal receiving waters in southern California. Combined, refineries and sewage treatment plants release approximately 214 kg day(-1) of MTBE into the marine environment, with Santa Monica Bay receiving most (98%) of this discharge. Dry weather urban runoff was analysed for samples collected from 25 streams and rivers, and accounted for less than 0.5% of the mass of MTBE discharged to coastal waters. Receiving water samples were collected from 23 stations in Santa Monica Bay, Los Angeles Harbour and Mission Bay or San Diego Bay. MTBE was detected at low concentrations near effluent discharges, however there was no evidence of baywide MTBE contamination related to these outfalls. Marinas and areas used intensively for recreational boating had the highest average MTBE concentration (8.8 microg l(-1)). Surface water contamination was most widespread in San Diego Bay and Mission Bay, areas with no refinery or sewage treatment plant inputs.     

Trace metals in sediments of Raritan bay

Marine sediments are the ultimate recipient of nearly all trace metals introduced by man into aquatic ecosystems. This study examined the amounts and distribution of six trace metals (Cd, Cr, Cu, Ni, Pb, Zn) in sediments of Raritan Bay, apolluted estuary. The highest levels of these metals found in Raritan Bay were: Cd-15, Cr-260, Cu-1230, Ni-50, Pb-985, Zn-815. Three metals regimes within Raritan Bay are readily apparent. An area of high values extends across the Bay from the mouth of the Raritan Riverand Arthur Killinto Sandy Hook Bay. This is bounded on the south and northeast by areas of somewhat lower concentrations. An area of relatively low concentrations, near background values, occupies the region at the mouth of the Bay between Sandy Hook peninsula and Coney Island, New York. Metals values from Raritan Bay are compared with other areas and with a few exceptions, the Raritan Bay maximum levels were similar in magnitude to those of areas in Corpus Christi Harbour (U.S.A), Severn Estuary (U.K.), Deep Sea and Florida Lakes, River Blyth (U.K.), dump sites off New York City, various basins off South California, and in Long Island Sound.     

Metals and organochlorines in dolphins and porpoises of Cardigan Bay,West Wales

Concentrations of seven metals (Cr, Ni, Cu, Zn, Cd, Hg, and Pb) and a range of organochlorine pesticides, individual chlorobiphenyl congeners, and total polychlorinated biphenyls (PCB) have been determined in tissues of dolphins, porpoises, seals, and a variety of food chain species and sediments from Cardigan Bay, West Wales. Elevated concentrations of metals were not seen in any of the animal tissues examined. Higher than expected levels of organochlorine compounds were found in tissues of dolphins and porpoises; these concentrations are not derived from local pollution, but come from the animals' normal diet which did not show markedly elevated levels of organochlorines. The level of organochlorine bioaccumulation seen in some of the cetaceans analysed is much higher than found previously; this may have serious health implications for populations of those species around the coasts of NW Europe.