Agrochemical and polychlorobyphenyl (PCB) residues in the Mekong River delta, Vietnam

An environmental survey on pesticide residues and polychlorobyphenyl compounds (PCBs), encompassing more than 70 polar and non-polar compounds quantifiable by the techniques used, was performed in the Mekong River delta based on analyses of water, sediment and bivalve mollusc samples. Few polar compounds, such as diazinon and fenotrothion, were detected in water but a high number of non-polar chlorinated compounds, such as DDT, HCH, endosulfan and PCBs, were detected in sediments and biota. The highest concentrations measured were of DDT with an average 6.3 ng g(-1) dry weight (range 0.32-67 ng g(-1)) in sediments and 38.6 ng g(-1) (range 5.5-123 ng g(-1)) in molluscs' soft tissues. Amongst chlorinated compounds, DDT concentrations were followed in decreasing order by those of PCB, endosulfan, hexachlorocyclohexane and chlordane. Residues of organochlorine compounds originate from local usage of agrochemicals although with a likely contribution also of atmospheric deposition of residues (not measured) originated elsewhere. Concentrations of PCB and pesticide residues in the aquatic environment of the Mekong River delta are lower than values reported for other regions of Vietnam and Asia. Nevertheless, current concerns about the effects of chlorinated compounds on public health advise improved control of chemical residue discharges in order to abate environmental contamination.     

Phosphorus dynamics in water and sediments in urbanized and non-urbanized rivers in Southern Brazil

Phosphorus flux models show that the removal tends to be a common feature in polluted estuarine systems whereas the release of P to the adjacent coastal area occurs in pristine environments. This study analyzes the distribution of P in water and sediments along six rivers in the south coast of Brazil. Three rivers located inside protected areas were considered non-polluted and used as a control of urbanization. The other three, situated within urbanized areas, were considered as having highly elevated concentrations of P. Results showed a different behavior of P in water and sediments located in urbanized and non-urbanized areas. The concentrations of dissolved organic (P-org) and inorganic (P-inorg) phosphorus in water, and the total phosphorus (P-tot) and polyphosphate (P-poly) in sediments where higher in the urbanized rivers compared to the non-urbanized ones. Both P of punctual origin and of diffuse origin contributed to the maintenance of elevated concentrations and disturbed the natural fluxes along the polluted rivers. The minimum and maximum concentrations in urbanized areas varied from 0.39 to 12.45 (microM) for P-org and 0.00 to 5.92 (microM) for P-inorg in water, and in sediments from 89.90 to 808.16 (microM g(-1)) for P-tot and 0.00 to 76.51 (microM g(-1)) for P-poly. In non-urbanized areas concentrations in water varied from 0.22 to 1.20 (microM) for P-inorg and 4.43 to 5.56 (microM) for P-org, and in sediments from 45.91 to 652.26 (microM g(-1)) for P-tot and 0.00 to 8.61 (microM g(-1)) for P-poly. Using a hierarchical sampling design and a simple model of variation of P (K(d) model) it was possible to demonstrate that urbanized and non-urbanized estuaries may act as sinks or sources of P. The variation of P analysis in different points along each of the six rivers showed that release and removal areas may occur within a same river independently of its urbanization.     

Antifouling biocides in water and sediments from California marinas

Irgarol 1051 is a common antifouling biocide and is highly toxic to non-target plant species at low ng/L concentrations. We measured up to 254 ng/L Irgarol in water and up to 9 ng/g dry weight Irgarol in sediments from Southern California recreational marinas. Irgarol’s metabolite, M1, concentrations were up to 62 ng/L in water and 5 ng/g dry weight in sediments. Another antifouling biocide, diuron, reached up to 68 ng/L in water and 4 ng/g dry weight in sediments. The maximum Irgarol concentrations in water were greater than the Irgarol concentration recommended as the plant toxicity benchmark (136 ng/L), suggesting that Irgarol concentrations may be high enough to cause changes in phytoplankton communities in the sampled marinas. Irgarol concentrations measured in sediments were greater than calculated Environmental Risk Limits (ERLs) for Irgarol in sediments (1.4 ng/g). Antifouling pesticide accumulation in sediments may present a potential undetermined risk for benthic organisms.     

Distribution and source apportionments of polychlorinated biphenyls (PCBs) in mariculture sediments from the Pearl River Delta, South China

Surface and core sediments collected from six mariculture farms in the Pearl River Delta (PRD) were analyzed to evaluate contamination levels of polychlorinated biphenyls (PCBs). The ∑PCBs (37 congeners) concentrations ranged from 5.10 to 11.0 ng g(-1) (mean 7.96 ng g(-1)) in surface and 3.19 to 22.1 ng g(-1) (mean 7.75 ng g(-1)) in core sediments, respectively. The concentrations were significantly higher than that measured in the sediments of their corresponding reference sites, whereby the average enrichment percentages were 62.0% and 42.7% in surface and core sediments, respectively. Significant correlations (R2=0.77, p<0.05) of PCB homologue group proportions between fish feeds and surface mariculture sediments suggested that fish feed input was probably the main source for the enrichment of PCBs. Due to the fact that PCBs could be transferred along food chains, PCB contamination in fish feeds and mariculture sediments should not be overlooked.     

Seasonal fluctuations of tissue mercury contents in the European shore crab Carcinus maenas from low and high contamination areas (Ria de Aveiro, Portugal)

The main objective was to study the seasonal variation of mercury concentrations in different tissues (muscle, hepatopancreas and gills) of Carcinus maenas from low and high Hg contaminated areas, a valuable resource in temperate estuaries and a possible pathway for human uptake. Individuals of two size classes (around 35 and 55 mm cephalothorax wide) were captured monthly between March 1999 and May 2000 in two areas of Ria de Aveiro: in the main navigation channel that connects the lagoon to the sea, and in the inner lagoon area heavily contaminated by mercury (maximum Hg in sediments of 5.4 microg g(-1)). Pronounced decreases in salinity and temperature and reduced food availability in winter seemed to be the responsible for the decline of the crab condition index (0.75-0.45) in larger individuals. Muscle and hepatopancreas exhibited higher mercury concentrations than gills, with concentrations in the contaminated site ranging from 0.03 to 0.63 microg g(-1) and 0.02 to 0.34 microg g(-1), respectively. Linear regressions between muscle and hepatopancreas (r=0.94, p<0.001) and muscle and gills (r=0.97, p<0.001) suggested a rapid redistribution of mercury inside the organism. During winter, a rapid elimination of mercury was found in the three analysed tissues followed by uptake. Larger crabs presented elimination rates from 18 to 34 ng g(-1) per week, while the smaller crabs showed lower elimination rates (10-24 ng g(-1) per week). The uptake was similar in both size classes (11-15 ng g(-1) and 8.1-15 ng g(-1) per week, respectively for large and small crabs). Our results suggest that C. maenas harvested in the contaminated areas must be considered with caution, since Hg concentrations were found to exceed the threshold concentration allowed for human consumption (0.5 microg g(-1)).     

A comparison of anthropogenic mercury pollution in Kastela Bay (Croatia) with pristine estuaries in Ore (Sweden) and Krka (Croatia)

Anthropogenic mercury pollution was studied in Kastela Bay (Croatia), 10 years after chloralkaline plant (PVC) stopped production. The concentration of total mercury determined in sediments which are composed mainly of calcite and quartz, are in the range 14,280-30,400 ng/g. The values are higher than reported in the literature for Elbe and Seine estuaries and also above 25,000 ng/g used for criterion in remediation project in Minamata Bay. The concentration of methylmercury 6.05-36.74 ng/g are typical for slightly to highly contaminated estuarine sediments. The low ratio of methylmercury to total mercury found in sediments of Kastela Bay is in the range 0.04-0.18%. It can be explained that in this region predominate conditions which do not promote in-situ methylation. Sediments were found to be highly anoxic. Concentrations of total mercury in unfiltered surface waters are in the range 69-145 ng/l and in unfiltered bottom waters in the range 230-1,418 ngl(-1). High concentrations found in bottom waters suggest that either resuspension or partial dissolution of sediments takes place. An experiment performed on filtered and unfiltered waters showed that about 85% of total mercury in surface water and almost 100% in bottom water was retained on 45 microm filters. To demonstrate contrasts, two pristine estuaries from norths and south Europe were studied. Silicious sediments of Ore estuary (Sweden) and calcareous sediments of Krka estuary (Croatia) have total mercury concentrations close to accepted background level. The ratio of methylmercury to total mercury is < or = 1% in all samples with one exception. The highest observed ratio (2.70%) was in the surface sediment from E2 station in Krka estuary measured in March 2000. This location is suitable for studying methylmercury formation in pristine environment.     

Perylene dominates the organic contaminant profile in the Berau delta, East Kalimantan, Indonesia

The geographical distributions of polyaromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), hexachlorobenzene, and 1,1-dichloro-2,2-bis(4-chlorophenyl)ethene (4,4'-DDE) were studied in the Berau delta (East Kalimantan, Indonesia), using sediment sampling and passive water sampling with semipermeable membrane devices. High concentrations of perylene were observed in sediments (54-580 ng g(-1) dry weight), and water (1-680 pg L(-1)). Perylene accounted for about 60% of the total concentrations of PAHs in the sediment. The relative abundance of the other PAHs was indicative of petrogenic sources. Concentrations of PCBs, hexachlorobenzene, and 4,4'-DDE in sediments were below or close to the detection limit (～ 0.02 ng g(-1)). The analysis of a sediment core revealed no appreciable changes in the concentration of target compounds over the past three decades. We show that sediment sampling and passive water sampling are complementary techniques, and propose to bring the results of both methods to the same concentration scale, using locally derived sediment-water partition coefficients.     

The distribution and inventory of total and methyl mercury in Kuwait Bay

Sediment (surface and core) sampling was conducted during the period from August 96-December 98 from intertidal and offshore areas in Kuwait Bay. The highest (and most variable) concentrations of total mercury (T-Hg; 36500+/-34930 ng g(-1)) are encountered around the previous industrial outfall where sediments are disturbed by shipping activities. The concentrations of T-Hg are lower in the Shuwaikh Port area (650+/-210 ng g(-1)) and continue to decrease towards the northern coastline of Kuwait Bay (average concentrations in the wider Bay region are 50+/-30 ng g(-1)). These values are still above background concentrations of 15-20 ng g(-1). Calculation of the total inventory of mercury in all the surface sediments of the studied area indicates that approximately 22.5 ton is present which is similar to the estimated industrial discharges of approximately 20 ton suggesting that the contamination is largely confined to the Bay and that releases to the wider Gulf region are small. The distributions of MeHg are similar to those of T-Hg and represent ranges between 0.23% and 0.5% of the T-Hg indicating that surface sediments within Kuwait Bay contain approximately 80 kg of this chemical.     

Evaluation of lindane diffusion along the southeastern Adriatic coastal strip (Mediterranean Sea): a case study in an Albanian industrial area

This study aimed to analyze the impact at sea of a pesticide factory located 7 km north of Durres (Albania) by investigating a lowland area under the sea situated 0.7 km from the shoreline. The main product of this factory was lindane. Production ceased in 1991 during the Albanian civil war, and a large amount of industrial waste was dispersed over the ground surrounding the factory, resulting in a high level of lindane pollution. A water-scoop channels the ground water accumulated around the disused factory directly into the sea. The concentrations of lindane in sediments collected along the coasts of the region ranged from 0.60 to 22.55 ng g(-1). The average concentration in the muscles of fish did not exceed the limits specified by European Commission legislation, whereas the concentration in the liver did exceed these limits; consequently, liver is not recommended for consumption.     

运河(杭州段)沉积物磷释放的模拟试验

采用室内模拟的方法研究了扰动情况下运河（杭州段）表层沉积物磷的释放对上覆水的影响以及投加石灰、投加三气氛发化铁、连续曝气、换水清洗等措施对沉积物磷释放的控制效果,研究表明,在扰动、开放体系条件下,运河（杭州段）沉积物磷释放导致的上覆水总磷浓度在释放初期最高,随时间逐渐下降,表现出净吸附,采集于有机污染较重河段的沉积物磷释放能力显著高于总磷含量较高但以重金属污染为主的河段的沉积物,上覆水投加石灰最终导致沉积物磷释放量的增加,投加三氯化铁显著降低了上覆水总磷浓度,上覆水连续曝气降低了上覆水的平衡磷浓度、换水清洗对上覆水磷浓度的降低效果是有限的,然而上述措施均未能将上覆水总磷浓度控制在V类水的浓度限定值以下,因此,就上覆水TP的浓度指标而言,运河（杭州段）沉积物的内源释放对其影响很大。     

Herbicide contamination and the potential impact to seagrass meadows in Hervey Bay, Queensland, Australia

Low concentrations of herbicides (up to 70 ng l(-1)), chiefly diuron (up to 50 ng l(-1)) were detected in surface waters associated with inter-tidal seagrass meadows of Zostera muelleri in Hervey Bay, south-east Queensland, Australia. Diuron and atrazine (up to 1.1 ng g(-1) dry weight of sediment) were detected in the sediments of these seagrass meadows. Concentration of the herbicides diuron, simazine and atrazine increased in surface waters associated with seagrass meadows during moderate river flow events indicating herbicides were washed from the catchment to the marine environment. Maximum herbicide concentration (sum of eight herbicides) in the Mary River during a moderate river flow event was 4260 ng l(-1). No photosynthetic stress was detected in seagrass in this study during low river flow. However, with moderate river flow events, nearshore seagrasses are at risk of being exposed to concentrations of herbicides that are known to inhibit photosynthesis.     

Characterization and composition of heavy metals and persistent organic pollutants in water and estuarine sediments from Gao-ping River, Taiwan

The objective of this study was to determine the concentrations and possible sources of heavy metals and persistent organic pollutants (POPs) in water and estuarine sediments from Gao-ping River in order to evaluate the environmental quality of aquatic system in southern Taiwan. High concentrations of heavy metals including Cr, Zn, Ni, Cu and As, ranging from 10.7 to 180 mg/kg-dry weight (dw), were detected in sediments from Gao-ping River. When normalized to the principal component analysis (PCA), swinery and electroplating wastewaters were found to be the most important pollution sources for heavy metals. Of various organochlorine pesticide (OCP) residues detected, aldrin and total-hexachlorocyclohexane (HCH) were frequently found in sediments. The total concentrations of OCPs were in the range 0.47-47.4 ng/g-dw. Also, the total-HCH, total-cyclodiene, and total-dichlorodiphenyltrichloroethane (DDT) were in the range 0.37-36.3, 0.21-19.0, and 0.44-1.88 ng/g-dw, respectively. The polychlorinated biphenyl (PCB) concentrations in sediments from Gao-ping River ranged between 0.37 and 5.89 ng/g-dw. The PCB concentrations are positively correlated to the organic contents of the sediment particles. alpha-HCH was found to be the dominant compound of HCH in the sediments, showing that long-range transport may be the possible source for the contamination of HCH in sediments from Gao-ping River. In summary, trace amounts of POPs in estuarine sediments from Gao-ping River were detected, showing that there still exist a wide variety of POP residues in the river sediments in Taiwan. These POP residues may be mainly from long-range transport and weathered agricultural soils, while heavy metal contamination is primarily from the swinery and industrial wastewaters.     

Development of the sediment and water quality management strategies for the Salt-water River, Taiwan

The Salt-water River watershed is one of the major river watersheds in the Kaohsiung City, Taiwan. Water quality and sediment investigation results show that the river water contained high concentrations of organics and ammonia-nitrogen, and sediments contained high concentrations of heavy metals and organic contaminants. The main pollution sources were municipal and industrial wastewaters. Results from the enrichment factor (EF) and geo-accumulation index (Igeo) analyses imply that the sediments can be characterized as heavily polluted in regard to Cd, Cr, Pb, Zn, and Cu. The water quality analysis simulation program (WASP) model was applied for water quality evaluation and carrying capacity calculation. Modeling results show that the daily pollutant inputs were much higher than the calculated carrying capacity (1050 kg day(-1) for biochemical oxygen demand and 420 kg day(-1) for ammonia-nitrogen). The proposed watershed management strategies included river water dilution, intercepting sewer system construction and sediment dredging.     

博斯腾湖沉积物中有机氯农药的分布特征及生态风险评价

对新疆博斯腾湖表层沉积物中有机氯农药进行分析,探讨其分布特征及来源,并对其生态风险进行评价.结果表明,沉积物中总有机氯农药的含量为2.15-16.80ng/g,其中氯丹和滴滴涕的含量较高,分别为0.12-12.08 mg/g、0.42-5.13ng/g·博斯腾湖总有机氯农药的含量从入湖口到湖心呈现出下降的趋势,说明其污...     

The use of surface-enhanced Raman scattering (SERS) for detection of PAHs in the Gulf of Gdańsk (Baltic Sea)

A field operable surface enhanced Raman scattering (SERS) sensor system was applied for the first time under real conditions for the detection of polycyclic aromatic hydrocarbons (PAHs) as markers for petroleum hydrocarbons in the Gulf of Gdańsk (Baltic Sea). At six stations, seawater samples were taken, and the sensor system was applied in situ simultaneously. These measurements were compared to the results of conventional GC/MS laboratory analysis of the PAH concentrations in the seawater samples. For a PAH concentration above 150 ng(12PAH)l(-1), there was agreement between the SERS sensor and the GC/MS determinations. A standard addition experiment yielded a PAH concentration of 900 ng l(-1) at the Gdańsk Harbor, which was of the same order as the GC/MS determinations of 12PAHs (200 ng(12PAH)l(-1)). The high SERS detection limit for seawater samples is explained by the competition for PAHs between the sensor membrane and particulate matter surfaces. Thus, the SERS sensor can be applied, e.g., as a non-quantitative alarm sensor for relatively high PAH concentrations in heavily polluted waters. The spectral unmixing procedure applied for Gdańsk Harbor water confirmed the presence of phenanthrene at the highest concentration ([Phe]=140 ngl(-1)) and of Chr (2.7 ng l(-1)), but it did not detect the other PAHs present in the Gdańsk Harbor water, as determined by GC/MS. When compared to the past literature and databases, the SERS spectra indicated the presence of a mixture of molecules consisting of carotenoids, n-alkanes, amines or fatty acids, and benzimidazoles at the coastal station ZN2. The spectra in the offshore direction indicated carboxylic acids. Interpretation of the farthest offshore in situ SERS measurements is difficult, principally due to the limited availability of reference spectra. The detection of the lower PAH concentrations commonly found in Baltic coastal water needs further research and development to obtain better sensitivity of the SERS sensor. However, the high analytical specificity of the SERS sensor also allows the detection of other chemical species that require the development of a SERS/Raman library for specific in situ spectral interpretation.     

Phosphorus retention and release by sediments in the eutrophic Mai Po Marshes, Hong Kong

This study examined the phosphorus retention and release characteristics of sediments in the eutrophic Mai Po Marshes in Hong Kong. Results of chemical fractionation show that the sum of inorganic P pools exceeded 50% of the total sediment P content, with the redox-sensitive iron-bound P (Fe(OOH) approximately P) being the dominant P fraction. Given the considerable average Fe(OOH) approximately P concentration of 912 microg g(-1), Mai Po sediments demonstrated a great potential to release bioavailable P under low sediment redox potentials. This was further supported by the high mean anaerobic P flux of 31.8 mg m(-2)d(-1) recorded in Mai Po sediment cores, indicating the role of bottom sediments as a net P source. Although sediments in Mai Po had appreciable Langmuir adsorption maxima (1642-3582 mg kg(-1)), the high zero equilibrium P concentrations (0.02-0.51 mg L(-1)) obtained suggest that sediment sorption processes would contribute to sustaining the eutrophic conditions in overlying water column even with a further reduction in external P load. Concerted efforts should be made to reduce internal loading of P, especially under reducing conditions, to complement the implementation of zero discharge policy for Deep Bay for effective eutrophication abatement and long-term water quality improvement in the Mai Po Marshes.     

非点源污染对太湖上游西苕溪流域水环境的影响

水资源短缺是全球性关注的问题,水质恶化更加剧了这一问题的严重性,定量研究水质变化及其影响凶素可为治理水环境提供基础依据．与实测数据及综合污染指数的对比表明,水质指数能够合理反映水质的变化程度和时空变化趋势．利用西苕溪流域1996-2000年水质监测数据的研究结果如下：西苕溪流域水质的空间变化趋势是自上游至下游逐渐恶化,时间变化的总体趋势是逐年转好;点污染源得到有效控制年份(1999年)的水质指数比以前年份(1996-1998年)有所提高但幅度不大,说明非点源污染是影响西苕溪流域水质的重要因素;流域水污染的主要形式是氮、磷污染,其主要非点源是农田、经济竹林和城镇径流及居民生活污水等．     

Occurrence of selected estrogens in mangrove sediments

This paper presents results related to the occurrence and distribution of estrogens along the Brazilian coast. Three mangrove areas were chosen to evaluate the presence of estrogens in surface sediments of mangrove forests. The presence of estrogens was observed in all studied sites. 17-α-Ethinylestradiol (EE2), a synthetic estrogen, was the most common and has been found in higher concentration (0.45-129.78 ng/g) compared to 17-β-estradiol (E1) and estrone (E2) (both being natural estrogens). The concentrations of E1 and E2 ranged from 0.02 to 49.27 ng/g and 0.03 to 39.77 ng/g, respectively. Theoretically, under anaerobic conditions EE2 can be reduced to E1 even in environments such as sediments of mangrove forests, which are essentially anaerobic. Even if the concentrations of estrogens seem to be insignificant in some samples, the effects remain uncertain.     

Transfer of organic contaminants to the Baltic in the Odra Estuary

This paper describes the transfer of organic contaminants to the sea, using PAHs (12 compounds) and PCBs (11 congeners) as examples, through a eutrophicated coastal lagoon (Szczecin Lagoon, on the Polish-German border). The transfer of contaminants study was based on their concentration in recent sediments (0-10 cm), in relation to different environmental conditions such as temperature, salinity, turbidity, oxygen and nutrients in water, hydrological conditions, organic carbon and biomarkers (pigments and their derivatives) in sediments. Results include the data obtained between 1994 and 2000, also those on before and afterwards the great flood in July 1997, at different stations in the Lagoon and the adjacent Pomeranian Bay. The results indicated that the eutrophic estuary of the shape of lagoon acts as an effective trap for the hydrophobic organic pollutants. The abundance and taxonomy of plankton as well as detritus derived from it play an important role in bonding the studied compounds. The salinity gradient in the lagoon has a significant influence upon deposition of the pollutants from the water column to the sediments and the residence time of the compounds there depends strongly on oxic-anoxic status of the sediments and the strength of interaction with sediments resulting from polarity, the type and stability of associates formed, as well as on hydrological conditions. We conclude that eutrophication in this area prevents pollution of the sea to some extent.