Impacts of pesticides in a Central California estuary

Recent and past studies have documented the prevalence of pyrethroid and organophosphate pesticides in urban and agricultural watersheds in California. While toxic concentrations of these pesticides have been found in freshwater systems, there has been little research into their impacts in marine receiving waters. Our study investigated pesticide impacts in the Santa Maria River estuary, which provides critical habitat to numerous aquatic, terrestrial, and avian species on the central California coast. Runoff from irrigated agriculture constitutes a significant portion of Santa Maria River flow during most of the year, and a number of studies have documented pesticide occurrence and biological impacts in this watershed. Our study extended into the Santa Maria watershed coastal zone and measured pesticide concentrations throughout the estuary, including the water column and sediments. Biological effects were measured at the organism and community levels. Results of this study suggest the Santa Maria River estuary is impacted by current-use pesticides. The majority of water samples were highly toxic to invertebrates (Ceriodaphnia dubia and Hyalella azteca), and chemistry evidence suggests toxicity was associated with the organophosphate pesticide chlorpyrifos, pyrethroid pesticides, or mixtures of both classes of pesticides. A high percentage of sediment samples were also toxic in this estuary, and sediment toxicity occurred when mixtures of chlorpyrifos and pyrethroid pesticides exceeded established toxicity thresholds. Based on a Relative Benthic Index, Santa Maria estuary stations where benthic macroinvertebrate communities were assessed were degraded. Impacts in the Santa Maria River estuary were likely due to the proximity of this system to Orcutt Creek, the tributary which accounts for most of the flow to the lower Santa Maria River. Water and sediment samples from Orcutt Creek were highly toxic to invertebrates due to mixtures of the same pesticides measured in the estuary. This study suggests that the same pyrethroid and organophosphate pesticides that have been shown to cause water and sediment toxicity in urban and agriculture water bodies throughout California, have the potential to affect estuarine habitats. The results establish baseline data in the Santa Maria River estuary to allow evaluation of ecosystem improvement as management initiatives to reduce pesticide runoff are implemented in this watershed.     

Determination of arsenic species in fish, crustacean and sediment samples from Thailand using high performance liquid chromatography (HPLC) coupled with inductively coupled plasma mass spectrometry (ICP-MS)

Suitable techniques have been developed for the extraction of arsenic species in a variety of biological and environmental samples from the Pak Pa-Nang Estuary and catchment, located in Southern Thailand, and for their determination using HPLC directly coupled with ICP-MS. The estuary catchment comprises a tin mining area and inhabitants of the region can suffer from various stages of arsenic poisoning. The important arsenic species, AsB, DMA, MMA, and inorganic arsenic (As III and V) have been determined in fish and crustacean samples to provide toxicological information on those fauna which contribute to the local diet. A Hamilton PRP-X100 anion-exchange HPLC system employing a step elution has been used successfully to achieve separation of the arsenic species. A nitric acid microwave digestion procedure, followed by carrier gas nitrogen addition- (N2)-ICP-MS analysis was used to measure total arsenic in sample digests and extracts. The arsenic speciation of the biological samples was preserved using a Trypsin enzymatic extraction procedure. Extraction efficiencies were high, with values of 82-102%(As) for fish and crustacean samples. Validation for these procedures was carried out using certified reference materials. Fish and crustacean samples from the Pak Pa-Nang Estuary showed a range for total arsenic concentration, up to 17 microg g(-1) dry mass. The major species of arsenic in all fauna samples taken was AsB, together with smaller quantities of DMA and, more importantly, inorganic As. For sediment samples, arsenic species were determined following phosphoric acid (1 M H3PO4) extraction in an open focused microwave system. A phosphate-based eluant, pH 6-7.5, with anion exchange HPLC coupled with ICP-MS was used for separation and detection of AsIII, AsV, MMA and DMA. The optimum conditions, identified using an estuarine sediment reference material (LGC), were achieved using 45 W power and a 20 minute heating period for extraction of 0.5 g sediment. The stability and recovery of arsenic species under the extraction conditions were also determined by a spiking procedure which included the estuarine sediment reference material. The results show good stability for all species after extraction with a variability of less than 10%. Total concentrations of arsenic in the sediments from the Pak Pa-Nang river catchment and the estuary covered the ranges 7-269 microg g(-1)and 4-20 [micro sign]g g(-1)(dry weight), respectively. AsV was the major species found in all the sediment samples with smaller quantities of AsIII. The presence of the more toxic inorganic forms of arsenic in both sediments and biota samples has implications for human health, particularly as they are readily 'available'.     

Relationships between trace elements in <Emphasis Type="Italic">Posidonia oceanica</Emphasis> shoots and in sediment fractions along Latium coasts (northwestern Mediterranean Sea)

The Mediterranean endemic seagrass Posidonia oceanica is widely used as a sensitive bioindicator of trace elements (TEs) in the coastal environment. Therefore, a bulk of data exist on TE levels from impacted versus unpolluted sites while only recent studies started comparing TE accumulation in plant compartments versus both water column and sediment characteristics. In this study, six TEs (As, Cd, Cr, Cu, Ni, Pb) were analyzed in P. oceanica shoots related to depth (?10 and ?20 m) and to TE concentrations in the different grain size fractions of the sediment, from two Sites of Community interest (SIC) in the central Tyrrhenian Sea. TE concentrations in both shoots and sediment were generally low, except for Cr. Cu was the only element showing significantly different concentrations at the two sites while As differed significantly between samples taken at different depths. TE concentrations in the unsieved sediment were found uncorrelated to TEs in shoots except for the important nutrient Cu (positive correlation). The finest sediment fractions were enriched in TEs and significantly correlated to Cd, Cr, Cu, and Ni concentrations in the shoots.     

Seasonal variation of nonylphenol concentrations and fluxes with influence of flooding in the Daliao River Estuary, China

Nonylphenol is an endocrine disruptor with harmful effects including feminization and carcinogenesis on various organisms. This study aims to investigate the distribution and ecological risks of nonylphenol in the Daliao River Estuary, China. Nonylphenol, together with other phenolic endocrine disruptors (bisphenol A, 4-t-butylphenol, 4-t-octylphenol, and 2,4-dichlorophenol), was detected in surface water and sediment on three cruises in May 2009, June 2010, and August 2010, respectively. A large flooding occurred during our sampling campaign in August and its effect on nonylphenol concentrations and fluxes in the estuary was therefore evaluated. The results showed that nonylphenol with a concentration range between 83.6–777 ng l^?1 and 1.5–456 ng?g^?1 dw in surface water and sediment was the most abundant among the phenolic compounds, accounting for 59.1–81.0 and 79.9–92.1 % of the total phenolic concentration in surface water and sediment, respectively. The concentrations recorded in May and June were comparable, whereas those in August were considerably higher, mainly due to the flush of flooding. The flooding also caused a 50 times increase in nonylphenol flux from the estuary into the adjacent Bohai Sea. Nonylphenol concentrations in the estuary have exceeded the threshold level of undesirable effects with a potential risk of harm to local species, especially benthic organisms.     

液相色谱-串联质谱法测定水体、沉积物及土壤中全氟化合物

建立了水、沉积物及土壤中13种全氟化合物(PFCs)的富集、净化、浓缩的前处理方法及快速液相色谱三重四级杆串联质谱的分析方法。9种全氟羧酸、2种典型全氟磺酸、2种磺酰铵衍生前体物的响应因子与质量浓度的线性关系良好。添加回收实验表明,13种全氟化合物在水、土壤和沉积物中的回收率为52.3%~119.3%,变异系数为2.3%~19.4%,方法检出限分别为0.015~0.472 ng/L、0.012~0.875 ng/g、0.004~0.743 ng/g。该法成功应用于实际样品的测定,沉积物和土壤中分别检测到3种和10种全氟化合物。     

Distribution of microbiological indicators of fecal pollution in the riverine substrates

Distribution of fecal microorganisms in water, periphyton, and sediment was studied along the ?rnovnica river (Croatia) over a 1.5-year period. It was found that periphyton was inhabited by the highest number of investigated bacteria, while lower numbers of them were found in sediment and the lowest in surface water of the river. The concentrations of fecal microorganisms in periphyton and partly in sediment were found to be significantly higher in the middle of the river course, near the town of ?rnovnica, while according to the analysis of surface water the highest degree of pollution was reached on its estuary. The results were explained with respect to bacterial?Calgal associations. Considering the fact that most of the river microorganisms are associated with periphyton and sediment particles and only a small number of them is in the free-living form, microbiological analysis of both periphyton and sediment together with water samples has been suggested when fecal pollution of a river is concerned.     

Anthropogenic plutonium in the North Jiangsu tidal flats of the Yellow Sea in China

The ^239+240Pu activities and ²⁴⁰Pu/²³⁹Pu atom ratios were analyzed using a double-focusing SF-ICP-MS for sediment core samples obtained in 2007–2008 from the North Jiangsu tidal flats in the Yellow Sea in China. Particular attention was focused on the ²⁴⁰Pu/²³⁹Pu atom ratios in the sediment to identify the origins of Pu isotopes. The profiles of ^239+240Pu activities in the sediment cores are similar to those of the ¹³⁷Cs activities. The ²⁴⁰Pu/²³⁹Pu atom ratios in the tidal flats showed typical global fallout values, indicating that this area did not receive the possible early direct close-in fallout or oceanic current transported Pu from the Pacific Proving Grounds (PPG). If any, the contribution of the PPG source Pu to the total Pu inventory is negligible. This is different from the sediments in the Yangtze River estuary in the East China Sea, where the PPG source Pu contributed ca. 45 % to the total inventory. In addition, the observation of the global fallout origin Pu in the North Jiangsu tidal flats indicated that the nuclear power plant in the region was not causing any alteration/contamination to the ²⁴⁰Pu/²³⁹Pu atom ratios. The ^239+240Pu and ¹³⁷Cs activities/inventories in the sediment cores showed correlation to the mean clay sediment compositions (fine particles) in the tidal flats. Therefore, mud deposits are served as sinks for the anthropogenic radionuclides in the tidal flats and the Yellow Sea. Integrated with the previously reported spatial distributions of ^239+240Pu and ¹³⁷Cs activities in the surface sediments of the Yellow Sea, the mechanism of Pu transport with the ocean currents and the scavenging characteristics in the Yellow Sea were discussed.     

饶河入鄱阳湖口处沉积物中重金属分布特征及形态研究

为了解饶河入鄱阳湖湖口重金属污染状况,在鄱阳湖饶河入湖段设置了3个采样点,用原子吸收分光光度计对沉积物进行了重金属Cu、Pb、Zn的测定,分析了这3种元素在各采样点的形态分布特征.结果表明:饶河人鄱阳湖口处沉积物中Cu、Pb、Zn的污染较为严重,呈现出复合污染的趋势.该区域沉积物中3种元素的分布受水流的影响较大,其形态...     

Effects of composition of labile organic matter on biogenic production of methane in the coastal sediments of the Arabian Sea

Coastal regions are potential zones for production of methane which could be governed by ecological/environmental differences or even sediment properties of a niche. In order to test the hypothesis that methanogenesis in most marine sediments could be driven more by proteins than by carbohydrates and lipid content of labile organic matter (LOM), incubation experiments were carried out with sediments from different environmental niches to measure methane production. The methane production rates were examined in relationship to the sediment biochemistry, i.e., carbohydrates, proteins, and lipids. The gas production measured by head space method ranged from 216 ng g(?-1) day(?-1) in the mangrove sediments to 3.1 μg g(?-1) day(?-1) in the shallow Arabian Sea. LOM ranged from 1.56 to 2.85 mg g(?-1) in the shallow Arabian Sea, from 3.35 to 5.43 mg g(?-1) in the mangrove estuary, and from 0.66 to 0.70 mg g(?-1) in the sandy sediments with proteins contributing maximum to the LOM pool. Proteins influenced methane production in the clayey sediments of shallow depths of the Arabian Sea (r = 0.933, p < 0.001) and mangrove estuary (r = 0.981, p < 0.001) but in the sandy beach sediments, carbohydrates (r = 0.924, p < 0.001) governed the net methane production. The gas production was more pronounced in shallow and surface sediments and it decreased with depth apparently governed by the decrease in lability index. Thus, the lability index and protein content are important factors that determine methane production rates in these coastal ecosystems.     

Perfluorooctane sulfonate (PFOS) distribution and effect factors in the water and sediment of the Yellow River Estuary, China

The distribution of perfluorooctane sulfonate (PFOS) was investigated in a total of 15 water and sediment samples from the Yellow River Estuary, China in April 2011. The results indicated that the concentrations of PFOS in the water and sediment samples averaged 157.5 ng/L and 198.8 ng/g and ranged from 82.30 to 261.8 ng/L and 75.48 to 457.0 ng/g, respectively. The concentrations of PFOS in the sediment column increased from 45.32 to 379.98 ng/g with the decrease of the sampling depth, which showed that the increased PFOS pollution in the sediment appeared in this region in over recent years. The distribution coefficient (K _d) of PFOS between water and sediment linearly increased from 0.37 to 4.80 L/g as the salinity (S‰) increased from 0.18 to 4.47. Correlation analysis revealed that K _d was significantly and positively correlated to the contents of total organic carbon and clay of the sediment, and salinity. Therefore, salinity was an important parameter in controlling the sediment–water interactions and the fate or transport of PFOS in the aquatic environment. The results of this study showed that the estuary was an important sink for PFOS and suggested that PFOS might be carried with the river water and transported for long distances before it reached to the sea and largely scavenged to the sediment in the estuaries due to the change in salinity.     

Integration of multi-disciplinary geospatial data for delineating agroecosystem uniform management zones

The aim of this study was the development of analytical methods for the simultaneous determination of 25 selected pharmaceuticals, metabolites, and pesticides, belonging to the various chemical classes, in river sediments and their corresponding surface and ground water with the purpose of monitoring the contamination levels. The methods were based on the solid-phase extraction as the sample preparation method for water samples, and the ultrasonic solvent extraction for the sediment samples, followed by the liquid chromatography–tandem mass spectrometry. High recoveries were achieved for extraction from both water and sediment samples for the majority of analytes. Low limits of detection were achieved for all investigated compounds in the water sample (1–5 ng L^?1) as well as in the sediment (1–3 ng g^?1). Applicability of the developed methods was demonstrated by determination of pharmaceutical and pesticide residues in 30 surface water, 44 groundwater, and 5 sediment samples from the Danube River Basin in Serbia. Sixty percent of target compounds were detected in environmental samples. The most frequently detected analytes in river sediments were the pesticides dimethoate and atrazine, while carbamazepine and metamizole metabolites 4-AAA and 4-FAA were the most frequently found in water samples.     

Fugacity approach to evaluate the sediment-water diffusion of polycyclic aromatic hydrocarbons

Diffusion is an important process for sediment-water exchange and plays a vital role in controlling water quality. Fugacity fraction (ff) was used to estimate the sediment-water diffusion of polycyclic aromatic hydrocarbons (PAHs) between seawater and surficial sediment. A total of 33 surface sediment and sea water samples were collected concurrently from the northeast coastal area in China and 25 PAHs were analyzed including the alkylated and chlorated PAHs. Fugacity fraction was calculated based on the PAH concentrations in water and sediment, octanol-water partition coefficient of PAHs, organic matter content in sediment, and density of sediment. The calculated results showed that ff increased with decreasing molecular weight of PAHs. The low molecular weight PAHs (2-3 rings) transferred from sediment to water and the sediment acted as a secondary source to the water. The medium molecular weight PAHs (4-5 rings) were close to the sediment-water equilibrium and the transfer tendency shifted between sediment and water. The high molecular weight PAHs (5-6 rings) transferred from water into sediment and the sediment acted as a sink. Soot carbon and the difference of PAH concentrations between sediment and water were found to be important factors affecting the sediment-water diffusion. This study provided new insight into the process of sediment-water diffusion, which has a great influence on the quality of water, especially in severely-polluted sediment areas.     

河口混合区划定及营养盐标准限值构建

河口是河流和海洋生态系统的过渡带,目前中国缺乏河口区划界和水质评价标准,河口区及其附近海域环境质量评价直接使用《海水水质标准》(GB 3097—1997)对标评价的方式,评价结果往往与实际不符,对河口地区开发建设和管理保护不利。笔者系统分析了中国河口区划分及水质评价的现状和存在问题,以北部湾主要入海河口钦州湾为例比较了河口区营养盐背景值与海洋营养盐背景值,两者差异显著,认为使用《海水水质标准》(GB 3097—1997)对河口区进行评价不能很好地反映环境质量。因此依据现行的《地表水环境质量标准》(GB 3838—2002)、《海水水质标准》(GB 3097—1997)和《近岸海域环境功能区管理办法》,提出使用盐度等数据探讨河口混合区划定及建立河口混合区水质营养盐标准限值的方法。在钦州湾的应用案例中,河口混合区的划定和河口区营养盐标准限值确定,都具有科学性和可操作性。使用河口混合区营养盐标准进行评价的结果比直接使用《海水水质标准》(GB 3097—1997)评价能更准确地反映环境质量,可为河口区划界及水质评价提供方法参考。     

环境中有机紫外吸收剂前处理及仪器分析方法研究进展

有机紫外吸收剂(OUVs)是广泛应用于个人护理品及工业产品的一种光稳定剂,也是一种新型"准"持久性有机污染物。由于环境样品基质复杂,且OUVs种类多、含量低,快速高效的样品前处理及准确灵敏的检测方法是提高OUVs监测精准度的基础。综述了自2005年以来环境样品中OUVs的常规前处理方法及分析方法。首先,在介绍水体、沉积物、生物样品前处理方法应用的基础上,分析了富集填料、洗脱剂、净化方法等实验条件对回收率的影响,目前在水体、沉积物、生物样品中,OUVs的回收率分别为14%~133.7%、30%~183%、46%~128%。其次,总结了质谱技术在OUVs分析中的应用,表明OUVs检测方法已经由传统的气相色谱-单四极杆联用逐渐过渡到液相色谱-串联质谱联用,并且着重阐述了离子源对OUVs信号强度影响的重要性。最后,结合OUVs监测现状,展望了环境样品中OUVs监测分析方法的发展趋势。     

Habitat Conditions and Correlations of Sediment Quality Triad Indicators in Delaware Bay

This paper summarizes sampling results from NOAA's National Status and Trends (NS&T) Program for marine environmental quality in Delaware Bay. A stratified-random design was used to determine the spatial extent of sediment contamination and toxicity in Delaware Bay from offshore stations in the coastal zone, the lower estuary, the upper estuary, the fresh/salt mixing zone, and tidal fresh areas. Sediment samples were taken for chemical analyses of major classes of environmental contaminants, a suite of toxicity bioassays, and benthic macrofaunal community assessment to identify patterns of resident species. The tidal-fresh areas and portions of the mixing zone of the study area were heavily contaminated. Contaminant concentrations were frequently above the 90th percentile of EMAP Virginian Province levels. PAHs in the sediment were higher than previously documented, with a major component of PAHs being pyrogenic in origin. Bioassay results were highly variable. Toxicity and contaminant levels were correlated when aggregated into indices, but were only marginally correlated with benthic community impacts. High and low abundance stations were found in all zones. Most of the tidal fresh stations were dominated by pollution tolerant species. Species diversity and abundance were generally lowest in the fresh/salt mixing zone.     

Spatial and temporal distribution of polycyclic aromatic hydrocarbons (PAHs) in sediments of the Nansi Lake, China

Polycyclic aromatic hydrocarbons (PAHs) were measured in surface sediments and dated core sediments from the Nansi Lake of China to investigate the spatial and temporal distribution characteristics. The concentrations of 16 kinds priority PAH compounds were determined by GC-MS method. And ²¹⁰Pb isotope dating method was used to determine the chronological age of the sediment as well as the deposition rate. The results indicated that the total PAHs concentration ranges in surface and core sediment samples were 160 ~32,600 and 137 ~ 693 ng/g (dry wt.), respectively. The sediment rate and the average mass sedimentation were calculated to be 0.330 cm·year^???1 and 0.237 g·cm^???2·yr^???1 and the sediment time of the collected core sample ranged from 1899 to 2000. The peak of PAH concentrations came at recent years. The source analysis showed PAHs mainly came from the contamination of low temperature pyrogenic processes, such as coal combustion. The PAHs concentrations were lower than ERL and LEL values for most collected samples. However, in several surface sediment samples especially in estuary sites, the PAHs concentrations were not only higher than ERL and LEL values, but also higher than ERM values.     

Characterization of heavy metals in water and sediments in Taihu Lake, China

To explore a comprehensive status of heavy metals in the Taihu Lake, which is one of the most important waters in China, water and sediment samples were taken throughout the lake during April to May of 2010, and metal elements (Cu, Cd, Cr, Ni, Pb, Sn, Sb, Zn, Mn) were analyzed in the water column, interstitial water and sediment. Relevant standards were used to assess the sediment and water quality. Results show that, in the lake water column, the average concentration of all metals ranged from 0.047 μg/l (Cd) to 8.778 μg/l (Zn). The concentration in the river water was usually higher than in the lake water for many metals. In the interstitial water Mn was significantly higher than that in water column, and other metals had no significant difference between the two media. In the surface sediment, average metal content ranged from 1.325 mg/kg (Cd) to 798.2 mg/kg (Mn). Spatially, contents of many metals were higher in Zhushan Bay than in other lake areas, and there existed a clear content gradient from the river to the lake for both water and sediment. On the sediment profiles, many metals presented an increasing trend from the depth of 15-20 cm to the top, which is indicative of the impact of increasingly intensive human activities from that period. Quality assessment indicates that metals in water phase are generally safe compared with USEPA "National Recommended Water Quality Criteria," with the exception of Mn in the interstitial water and Sb in the river water. Whereas the sediment is widely contaminated with metals to some extent compared with the "Consensus-Based Sediment Quality Guidelines," and Cu, Cr, and Ni are more likely to raise ecological risks. This work could be a basis for the ongoing China's criteria strategy.     

Primary Productivity in the Golden Horn

The shores of the Golden Horn—once most important seaport of the region—represented throughout history a romantic and recreational venue. This tributary to the Bosphorus, however, became seriously polluted with the extensive industrialization and rapid population growth in Istanbul over the past century. Two main tributaries, the Alibeykoy and the Kagithane, dumped both liquid and solid waste from residential areas and industry (small and large-scale) into the Golden Horn. As a result of this pollution, the landward three to four kilometers of the estuary became swamped with sediment. The dominance of anaerobic activity resulted in a highly unpleasant smell, and the shallow depth as one progressed up the bay restricted navigation. In early 1997 The Istanbul Metropolitan Municipality began a dredging operation and gradually diverted all domestic and industrial wastewater discharge from the Golden Horn. Since then there have been remarkable improvements in water quality. This paper presents the state of eutrophication through the water body of the Golden Horn; parameters such as DO, TKN, NH₃-N, NO₃-N, the total phosphorus (TP) and dissolved phosphorus (PO₄-P), phytoplankton and chlorophyll-a have been were analyzed in samples of water taken from various points in the Golden Horn. The presence of DO and the phytoplankton, both indicators of primary productivity in an aquatic body, has been evaluated in relation to former conditions.     

Occurrence and sorption properties of arsenicals in marine sediments

The content of total arsenic, the inorganic forms: arsenite (As(III)) and arsenate (As(V)), the methylated forms: monomethylarsonic acid and dimethylarsinic acid (DMA), trimethylarsenic oxide, tetramethylarsenonium ion and arsenobetaine was measured in 95 sediment samples and 11 pore water samples from the Baltic Sea near the island of Bornholm at depths of up to 100 m. As(III+V) and DMA were detected in the sediment and As(III+V) was detected in the sediment pore water. Average total As concentration of 10.6?±?7.4 mg/kg dry matter (DM) in the sediment corresponds to previously reported values in the Baltic Sea and other parts of the world. Existing data for on-site measurements of sorption coefficients (Kd) of arsenicals in marine and freshwater sediments show large variability from <1 to >1,000 L/kg. In this work, calculated sorption coefficients (Kd and Koc) for As(III+V) showed significant correlation with depth, dissolved oxygen (DO), salinity and sediment classification; for depths <70 m, salinity <11 %, DO >9 mg/L and sand/silt/clay sediments the Kd was 118?±?76 L/kg DM and for depths >70 m, salinity >11 %, DO?<?9 mg/L and muddy sediments the Kd was 513?±?233 L/kg DM. The authors recommend using the found Kd value for arsenic in marine sediments when conditions are similar to the Baltic Sea. At locations with significant anthropogenic point sources or where the local geology contains volcanic rock and sulphide mineral deposits, there may be significantly elevated arsenic concentrations, and it is recommended to determine on-site Kd values.     

Probabilistic risk assessment and risk mapping of metals in tropical estuarine sediments using the 1 quarisk model

Total sediment concentrations of Cd, Cu, Pb, Zn, As, and Hg obtained from the Ankobra, Sakumo II, and Volta estuaries in Ghana were used to generate contaminant probability density distributions and species sensitivity distributions in AQUARISK. Results of the tier 1 assessment showed Cu, Cd, Zn, and Pb were not of concern in the Ankobra as their measured values and the 99th percentile of the fitted distributions were lower than the SQG low-trigger values. Mercury (Hg) and As were however, identified to be of concern in this estuary. In the Sakumo II estuary, Cu, Cd, Pb, and Hg have been identified to be of concern because their concentrations are higher than the SQG low-trigger values. Hg has been identified as the only metal of concern in the Volta estuary. The total proportion of species likely to be affected by the combined concentration of Cd, Cu, and Zn measured from Ankobra, Sakumo II, and Volta were 14%, 16%, and 12%, respectively, according to the Bur III distributional analysis of the ecotoxicology data. The measured median sediment concentrations of As and Hg in the Ankobra estuary greatly exceeded the median sediment concentration targets to achieve a 5% or less exceedence of the SQG low value. Similarly, in the Sakumo II estuary, the measured median sediment concentrations of Cu, Pb, and Hg greatly exceeded the median sediment concentration targets to achieve a 5% or less exceedence of the SQG low. For the Volta estuary however, other metals except Hg fall below the target values.