Distribution Of Organic Contaminants Research Articles

Key role of plankton species and nutrients on biomagnification of PAHs in the micro-food chain: A case study in plateau reservoirs of Guizhou, China

There is considerable inconsistency in results pertaining to the biomagnification of PAHs in aquatic systems. Zooplankton specifically play an important role controlling the fate and distribution of organic contaminants up the food chain, particularly in large plateau reservoirs. However, it remains largely unknown how secondary factors affect the magnification of organic compounds in zooplankton. The present study assessed plankton species and nutrients affecting the trophic transfer of PAHs through the micro-food chain in plateau reservoirs, Guizhou Province China. Results show soluble ∑PAHs range from 99.9 – 147.3 ng L-1, and concentrations of ∑PAHs in zooplankton range from 1003.2 - 22441.3, with a mean of 4460.7 ng g-1 dw. Trophic magnification factors (TMFs) > 1 show biomagnifications of PAHs from phytoplankton to zooplankton. The main mechanisms for trophic magnification > 1 are 1) small Copepoda, Cladocera and Rotifera are prey for larger N. schmackeri and P. tunguidus, and 2) the δ15N and TLs of zooplankton are increasing with the increasing nutrients TN, NO3- and CODMn. As a result, log PAHs concentrations in zooplankton are positively correlated with the trophic levels (TLs) of zooplankton, and log BAFs of the PAHs in zooplankton are increasing with increasing TLs and log Kow. Temperature further enhances TMFs and biomagnifications of PAHs as noted by temperature related reductions in δ15N. There are also available soluble PAHs in the water column which are assimilated with increasing phytoplankton biomass within the taxa groups, diatoms, dinoflagellates and chlorophytes. Notable TMFs of PAHs in zooplankton in Guizhou plateau reservoirs are not significantly affected by phytoplankton and zooplankton biomass dilutions. The present study demonstrates the important roles of species selection, nutrients and temperature in the environmental fate of PAHs in freshwaters.

Ecological risk assessment, source identification and spatial distribution of organic contaminants in terms of mucilage threat in streams of Çanakkale Strait Basin (Türkiye)

In this study, the spatial distributions of organic contamination stressors in water of fluvial habitats in the Çanakkale Strait (ÇS) watershed were investigated and the data were assessed in terms of human health and mucilage threat. Seven significant riverine ecosystems flowing into the ÇS were defined in the basin. Water samples were taken in the spring season (2023), when the phytoplankton communities reach their highest densities. Then they were tested for a total of 8 limnological parameters.The Nutrient Pollution Index (NPI) and Water Quality Index (WQI) were applied to assess the comprehensive quality characteristics of waters. The Hazard Quotient (HQ) and Hazard Index (HI) were applied to indicate the prospective non-carcinogenic human health risks of organic stressors. Principal Component Analysis (PCA) and Cluster Analysis (CA) were applied to categorize the investigated habitats and define the sources of investigated contamination parameters. Also, Geographic Information System (GIS) was used to make an effective assessment through visualization.The determined spatial mean values of the measured variables in ÇS watershed as follows: 18.21 °C for temperature, 8.51 mg/L for DO, 4.57 NTU for turbidity, 3.95 mg/L for suspended solids, 1.11 mg/L for NO3–N, 0.012 mg/L for NO2–N; 0.173 mg/L for PO4–P and 2.32 mg/L for BOD. It has been determined that the organic pollution loads and water temperature values of the investigated sub-basins increase from the upstream to the downstream locations and Çanakkale Stream was recorded as the riskiest fluvial habitat for the ÇS watershed. According to the results of health risk assessment indices, non-carcinogenic risks of organic pollutants would not be expected for all age groups.

Elucidating the spatial distribution of organic contaminants and their biotransformation products in amphipod tissue by MALDI- and DESI-MS-imaging

The application of mass spectrometry imaging (MSI) is a promising tool to analyze the spatial distribution of organic contaminants in organisms and thereby improve the understanding of toxicokinetic and toxicodynamic processes. MSI is a common method in medical research but has been rarely applied in environmental science. In the present study, the suitability of MSI to assess the spatial distribution of organic contaminants and their biotransformation products (BTPs) in the aquatic invertebrate key species Gammarus pulex was studied. Gammarids were exposed to a mixture of common organic contaminants (carbamazepine, citalopram, cyprodinil, efavirenz, fluopyram and terbutryn). The distribution of the parent compounds and their BTPs in the organisms was analyzed by two MSI methods (MALDI- and DESI-HRMSI) after cryo-sectioning, and by LC-HRMS/MS after dissection into different organ compartments. The spatial distribution of contaminats in gammarid tissue could be successfully analyzed by the different analytical methods. The intestinal system was identified as the main site of biotransformation, possibly due to the presence of biotransforming enzymes. LC-HRMS/MS was more sensitive and provided higher confidence in BTP identification due to chromatographic separation and MS/MS. DESI was found to be the more sensitive MSI method for the analyzed contaminants, whereas additional biomarkers were found using MALDI. The results demonstrate the suitability of MSI for investigations on the spatial distribution of accumulated organic contaminants. However, both MSI methods required high exposure concentrations. Further improvements of ionization methods would be needed to address environmentally relevant concentrations.

Study of the presence and environmental risk of organic contaminants policed by the European Union and other organic compounds in the water resources of a region overlapping protected areas: The Guadiaro River basin (southern Spain)

The study presented here is a first qualitative assessment of the occurrence of organic contaminants contemplated and not yet contemplated in European Union environmental legislation in water resources in the little anthropized Guadiaro River basin (70% of its area is covered by natural vegetation), in southern Spain. Water samples were collected from four carbonate aquifers, two detrital aquifers and four surface water courses and were analyzed for (i) 171 organic contaminants, (ii) major ions and (iii) stable isotopes (δ18OH2O, δ2HH2O, δ13CDIC). An environmental risk assessment was conducted through calculation of risk quotients comparing measured concentrations with ecotoxicological data found in the literature. Twenty-five organic contaminants were detected, at least once, including pesticides, pharmaceuticals, drugs of abuse and polycyclic aromatic hydrocarbons (PAHs). Cocaine and its main metabolite were detected in 85% and 95% of water samples, respectively (0.001–0.18 μg/L and 0.004–0.6 μg/L, respectively). Pyrene (PAH) was found in all water samples (0.001–0.015 μg/L) and forest fires were pointed out as a potential diffuse source. Relationship between rivers and aquifers is reflected by the distribution of organic contaminants, essentially the drugs of abuse. Concentration of contaminants were generally higher in groundwater samples, especially from detrital aquifers, potentially due to an accumulation process promoted by irrigation-return flows and by its slow dynamic compared to that of karstic systems. Pyrene concentration was also higher in some springs from karstic aquifers. Hence, calculated risk quotients were in general higher in groundwater, meaning that the threat to surface aquatic systems can grow as aquifers increase their influence on the water courses as the dry season progresses. The relationship between δ13CDIC and most organic contaminants (especially pyrene) reveal the role of the soil as storage media.

Geochemical and Geospatial Distribution of Organic Contaminants in the Flood Plain of Ekpetiama, Niger Delta Region of Nigeria

This study investigated the geochemical and geospatial distribution of organic contaminants in the floodplain water and sediments of Ekpetiama in the Niger Delta Region of Nigeria. This study is necessary because there are limited data on the level of organic contamination in this section of the Niger Delta Region of Nigeria. The extinction of planktons in Ekpetiama became a source of concern to the residents. This concern is because this section of the coastal plain provides fisher folks with livelihood. So, there was a need to track the source of contamination in this part of the Niger Delta region. Previous studies have suggested a high level of Total Petroleum Hydrocarbon and Total Hydrocarbon Content as possible sources of reduced dissolved oxygen in similar deltaic terrain. A total of 10 water and 10 sediment samples were collected and analyzed in triplicate at an interval of 100 m in the flood plain. A particle size analyzer was used to perform particle size analyses of air-dried sediments. The American Public Health Association method (APHA) was used to do the chemical analysis of the water samples. Here, a liquid-liquid extraction procedure was performed on sediment samples using 30 mL of Dichloromethane (DCM) as the extracting agent. The results were subjected to statistical validation. The mean grain size ranged from 2.37-4.83, kurtosis (1.94-0.49), and skewness (-0.8-0.71). The contaminant indicators (pH, biochemical oxygen demand, chemical oxygen demand, dissolved oxygen and Total Organic Carbon) point to the presence of organic contamination of the flood plain. The results indicated a total petroleum hydrocarbon range of 0.47-0.87 ppm in water and 0.69-0.96 ppm in sediments and a total hydrocarbon content range of 1.10-2.80 ppm in water and 2.56-3.90 ppm in sediment# samples. The results were above the permitted limits of the World Health Organisation. The source of ecological damage is the abnormal concentrations of organic contaminants in the flood plain. These results significantly caused ecosystem damage and human health effects in the food chain. This study provides information to the National Oil Spill Detection and Response Agency for a cleanup process.

Geochemical and Geospatial Distribution of Organic Contaminants in the Flood Plain of Ekpetiama, Niger Delta Region of Nigeria

This study investigated the geochemical and geospatial distribution of organic contaminants in the floodplain water and sediments of Ekpetiama in the Niger Delta Region of Nigeria. This study is necessary because there are limited data on the level of organic contamination in this section of the Niger Delta Region of Nigeria. The extinction of planktons in Ekpetiama became a source of concern to the residents. This concern is because this section of the coastal plain provides fisher folks with livelihood. So, there was a need to track the source of contamination in this part of the Niger Delta region. Previous studies have suggested a high level of Total Petroleum Hydrocarbon and Total Hydrocarbon Content as possible sources of reduced dissolved oxygen in similar deltaic terrain. A total of 10 water and 10 sediment samples were collected and analyzed in triplicate at an interval of 100 m in the flood plain. A particle size analyzer was used to perform particle size analyses of air-dried sediments. The American Public Health Association method (APHA) was used to do the chemical analysis of the water samples. Here, a liquid-liquid extraction procedure was performed on sediment samples using 30 mL of Dichloromethane (DCM) as the extracting agent. The results were subjected to statistical validation. The mean grain size ranged from 2.37-4.83, kurtosis (1.94-0.49), and skewness (-0.8-0.71). The contaminant indicators (pH, biochemical oxygen demand, chemical oxygen demand, dissolved oxygen and Total Organic Carbon) point to the presence of organic contamination of the flood plain. The results indicated a total petroleum hydrocarbon range of 0.47-0.87 ppm in water and 0.69-0.96 ppm in sediments and a total hydrocarbon content range of 1.10-2.80 ppm in water and 2.56-3.90 ppm in sediment# samples. The results were above the permitted limits of the World Health Organisation. The source of ecological damage is the abnormal concentrations of organic contaminants in the flood plain. These results significantly caused ecosystem damage and human health effects in the food chain. This study provides information to the National Oil Spill Detection and Response Agency for a cleanup process.

Occurrence, sources and environmental risk assessment of organic micropollutants in coastal sediments from the Atacama Region (Chile)

Nowadays, there is still a scientific knowledge gap regarding occurrence and distribution of organic contaminants in remote areas. In this study, we have monitored for the first time the presence of a wide range of persistent and emerging organic pollutants in the Atacama Desert coastal region (Chile), a key area in the Humboldt Current System. Nonylphenols (NPs), polycyclic aromatic hydrocarbons (PAHs), pesticides, UV filters, synthetic fragrances, and organophosphate flame retardants (OPFRs) were determined in sediments along the >500 km length Atacama coastline. NPs, well-known endocrine disruptors, were the predominant pollutants in the area (up to 333.5 ng g−1 dw). We identified inputs of different classes of contaminants from anthropogenic activities such as mining, agriculture, direct effluent discharges, harbors, energy plants, recreational activities, and tourism occurring along the coastline. Environmental risk assessment through calculation of hazard quotients (HQs) showed a high ecological risk level for NPs in the three provinces of Atacama (HQ >1). In the case of PAHs, (pyrene, benz(a)anthracene, chrysene, acenaphthene, naphthalene and benzo(a)pyrene) HQ >1 was showed in Copiapó province. Furthermore, estradiol equivalent concentrations (EEQ) were determined to estimate estrogenicity of the environmental sediment samples. The maximum EEQ value was for NPs in H1 (Carrizal Bajo wetland), province of Huasco, where the highest concentration of NPs was found. The sampling point H1 is a particular location because it is the exit of a wetland and a tourist point used as a beach. The potential risks of anthropogenic chemical substances impacting remote regions such as the one studied here highlight the need of expand monitoring efforts worldwide for a better assessment of the global pollution status.

Two-Compartmental Toxicokinetic Model Predicts Interspecies Sensitivity Variation of Imidacloprid to Aquatic Invertebrates.

Interspecies sensitivity to the same chemical can be several orders of magnitude different. Quantifying toxicologically internal levels and toxicokinetic (TK) parameters is critical in elucidating the interspecies sensitivity. Herein, a two-compartmental TK model was constructed to characterize the uptake, distribution, and elimination kinetics toward interspecies sensitivity to an insecticide, imidacloprid. Imidacloprid exhibited the highest lethality to the insect Chironomus dilutus, followed by Lumbriculus variegatus, Hyalella azteca, and Daphnia magna. Interspecies sensitivity of imidacloprid to these invertebrates varied by ∼1000 folds based on water concentrations (LC50). Remarkably, the sensitivity variation decreased to ∼50 folds based on the internal residues (LR50), highlighting the critical role of TK in interspecies sensitivity. A one-compartmental TK model failed to simulate the bioaccumulation of imidacloprid in these invertebrates except for D. magna. Instead, a two-compartmental model successfully simulated the slow elimination of imidacloprid in the remaining three species by internally distinguishing the highly dynamic (C1) and toxicologically available (C2) fractions. We further showed that the species sensitivity of the invertebrates to imidacloprid was significantly related to C2, demonstrating that C2 was toxicologically available and responsible for the toxicity of imidacloprid. This mechanistic-based model bridged the internal distribution of organic contaminants in small invertebrates and the associated toxic potency.

In-situ biological effects, bioaccumulation, and multi-media distribution of organic contaminants in a shallow lake

Anthropogenic activity-impacted aquatic environment contains a complex mixture of contaminants, and ecological risk assessment solely based on chemical analysis is insufficient and biological assessment is required. However, traditional assessment heavily relies on laboratory bioassays, which may cause uncertainty due to inevitable laboratory-related artifact. A self-designed in-situ bioassay system was successfully applied to simultaneously evaluate water and sediment toxicity by co-exposure of two native species, Chinese rare minnows (Gobiocypris rarus) and Asian clams (Corbicula fluminea) in Tai Lake Basin, China. In-situ exposure caused pronouncedly lethal and sublethal effects (i.e., metabolic and oxidative stress, neurotoxicity, reproductive toxicity) on both fish and clams. Meanwhile, multi-media distribution of organic contaminants in water-sediment-biota system was analyzed. Besides hydrophobicity, metabolism was recognized as an influential factor on phase distribution of contaminants in water-fish and sediment-clam systems. Traditional hazard quotient (HQ) method based on environmental concentrations of 98 contaminants showed bias in risk assessment. Instead, a weight of evidence method by integrating three lines of evidence, including in-situ survival, enhanced integrated biomarker response values and environmental concentrations, successfully differentiate high- and moderate-risk sites in the shallow lakes. The present study incorporated in-situ bioassays into risk assessment using a weight of evidence approach, which reduced uncertainty in decision-making.

Persistent organic pollutants (POPs) in fish species from different lakes of the lesser Himalayan region (LHR), Pakistan: The influence of proximal sources in distribution of POPs

Fish dwelling in remote mountain water systems are sensitive to long term exposure of POPs and can be used as an important bioindicator of POPs pollution in fragile mountain ecosystems. Current study aimed to investigate the concentrations and patterns of organic pollutants in fish tissues from different lakes of the Lesser Himalayan Region (LHR). OCPs, PCBs, PBDEs were analyzed in four common edible fish species of the LHR: Oncorhynchus mykiss, Labeo rohita, Hypophthalmichthys molitrix and Orechromis aureus. The fish were collected from lakes with different types of catchment areas (glacial, non-glacial mountain region and urban region) and extent of anthropogenic influence. The levels OCPs, PCBs and PBDEs analyzed in the selected fish species were in range of 0.21–587, 6.4–138 and 1.2–14 ng g−1 lw, respectively. The ∑DDTs, higher chlorinated PCBs, tetra- and penta-BDEs were more prevalent in urban and remote lakes whereas pp’-DDE, lower chlorinated PCBs and BDE-47 and -99 were predominant in fish species from glacial lakes. ∑DDTs, ∑PCBs and ∑PBDEs showed statistically significant differences (p < 0.05) among species, trophic guilds (carnivore, herbivore and omnivore) and feeding regimes (surface, bottom and column feeder) and ∑HCH showed a significant difference only among trophic guilds. The stable isotope values of δ 15N and δ13C differed significantly among species for ∑HCH, ∑PCBs, ∑PBDEs (p < 0.05) and ∑DDT (p < 0.01). The range of δ13C values (−34 to −19‰) indicated the importance of littoral and pelagic sources of dietary carbon. Trophic position and dietary proxies were identified as important variables for explaining the variability of the studied compounds. Kohonen self-organizing maps (SOM) showed that in addition to trophic position and other physiological characteristics of fish, that the type of lakes and proximal sources of POPs were the most important predictors for distribution of organic contaminants in fish samples from LHR.

Polycyclic aromatic hydrocarbons in urban Greenland soils of Nanjing, China: concentration, distribution, sources and potential risks.

In order to better study the influence of land use on the concentration and distribution of organic contaminants in urban areas, the concentrations of 16 principal polycyclic aromatic hydrocarbons (PAHs) were determined on soil samples collected at three depths (0~10cm, 10~20cm and 20~30cm) from urban greenland areas of 6functional zones: residential zone (RZ), business zone (BZ), industrial zone (IZ), cultural and educational zone (CZ), urban park (UP) and urban rural forest (URF) of Nanjing, China. Results showed that the average concentration of ∑PAHs in the urban greenland of Nanjing (499.47ng/g) was comparable to the value reported for other cities under similar conditions. Acenaphthene was the dominant compound (46.2% of the ∑PAHs), and low molecular weight PAHs (LPAHs) represented the largest share of ∑PAHs. Concentrations of ∑PAHs in 6 function zones were different, with the highest value in IZ (954.33ng/g) and lowest value in URF (147.81ng/g). The soil showed the highest ∑PAHs contamination in the layer 10~20cm in all zones (on average 547.01ng/g). ∑PAHs of IZ showed the highest values in all soil layers. Isomer ratio and factor analysis were used to determine the source of PAHs in soil. Petroleum combustion (PC), coal and biomass combustion (CBC), mixed (M) and petroleum (P) sources were finally identified as the four main sources of PAHs in Nanjing urban greenland soil, accounting for 50.2%, 14.9%, 8.4% and 6.6%, respectively. Bap toxic equivalent (TEQBap) was used to analyze the ecological risk. TEQBap was 20.59ng/g in total zones (TZ), below the threshold for multipurpose soil of Dutch legislation (32.96ng/g), but 69% of samples exceeded this threshold. TEQBap of different functional zones is ordered as: IZ (43.62ng/g)>RZ (23.89ng/g) > BZ (20.62ng/g) > CZ (19. 93ng/g) > UP (12.97ng/g) > URF (2.01ng/g). In the industrial area, more than 97% of TEQBap depended on seven carcinogenic PAHs (∑PAH7c), which indicated that IZ had high ecological risk. Lifetime risk of cancer (ILCR) model was used to assess the health risk of ∑PAHs. ILCRs ranked as following: children > youth > adults, with soil oral intake determining the highest cancer risk, followed by skin contact and breath intake. ILCRs of children were in high cancer risk range, with values of 3.77 × 10-4 (for boy) and 3.87 × 10-4 (for girl), while ILCRs of youth and adults were in an acceptable range; ILCRs were highest in IZ, followed by RZ, BZ, CZ, UP and URF. The soil PAHs analysis in different function greenland zones of Nanjing showed that land use influenced the concentration and distribution of PAHs in soils. This difference should be taken into account in the urban greenland planning and management to reduce the risks for the environment and human health.

Concentration, characterization and risk assessment of polycyclic aromatic hydrocarbons and organochlorine pesticides in soils from the Corn Belt of northeast China

AbstractOrganic contaminants in agricultural soils are widely reported; however, their accumulation patterns are quite different among regions. This study reports the distribution, accumulation and risk assessment of polycyclic aromatic hydrocarbons (PAHs), dichlorodiphenyltrichloroethane (DDT) and hexachlorocyclohexane (HCH) in soils from the Corn Belt of northeast China at a regional scale. Concentrations of PAHs, DDT and HCH were 306‐5300, 6.00–82.0 and 4.07–15.6 ng g−1, respectively. Source analysis suggests PAHs were derived from regional combustion of biomass and coal, except where sites are strongly affected by local sources. The DDT and HCH residues in soils are likely to be derived from previous agricultural applications that have persisted due to slow microbiological degradation under low mean temperatures. Precipitation was only significantly correlated with PAH concentrations, suggesting that precipitation affected PAH but not DDT and HCH distributions at a regional scale. Positive correlations between DDT concentrations and total organic carbon (TOC) contents of soils suggest hydrophobic organic contaminants were associated with organic matter. In contrast, TOC contents were correlated with PAHs in alfisols but not in pedocals. Pedocals contained mainly high molecular weight PAHs, indicating that eluviation affected the accumulation of less hydrophobic organic contaminants. Different correlations between low‐molecular‐weight PAH and HCH concentrations with TOC contents were found in alfisols, suggesting that contaminant structure may also affect the accumulation of less hydrophobic organic contaminants in these soils. Risk analysis suggested that potential ecological risks related to soils in the Corn Belt may lead to reduced maize production and the potential for human health risks in the future.Highlights Few studies focus on regional‐scale factors that affect organic contaminant accumulation in soils. Environmental process affects less hydrophobic organic contaminant distribution at regional scale. Precipitation and eluviation affected accumulation of less hydrophobic contaminants in soils. PAH and OCP residues in the soil of maize fields may pose ecological risks affecting future crop production and human health.

Evaluation of factors influencing annual occurrence, bioaccumulation, and biomagnification of antibiotics in planktonic food webs of a large subtropical river in South China

Biological pump is important to control the fate and distribution of organic contaminants, particularly in temperate and cold oligotrophic waters. However, it remains largely unknown how factors affect the long-term occurrence and fate of ionogenic organic compounds in subtropical eutrophic waters. The present study aimed to assess biogeochemical and physical factors affecting the annual occurrence, bioaccumulation, and trophic transfer of 14 antibiotics through planktonic food webs in the Pearl River, a large subtropical eutrophic river in China. This was done by carrying out 1-year simultaneous field observations of antibiotic concentrations in five water column compartments and assessing the variability of bioconcentration (BCF), bioaccumulation (BAF), and biomagnification (BMF) factors, which were influenced by plankton biomass, pH and temperature of water columns. The annual mean antibiotic concentration per site ranged from 1014.66 ± 535.66 ng L−1 to 1464.63 ± 1075.91 ng L−1, and was positively correlated with phytoplankton biomass, but independent of the proximity of the sites to urban areas. Antibiotic occurrences in both phytoplankton and zooplankton were greatly influenced by a biodilution effect. The annual occurrence of antibiotics in the water column was modulated by biological pumps as well as their equilibrium partitioning, and indirectly influenced of eutrophication with pH increased with phytoplankton biomass and phytoplankton life cycling. BAF of antibiotics by plankton had biphasic correlations with temperature (n = 150, R2 = 0.17–0.60, p < 0.001) and decreased with plankton biomass (n = 105–147, R2 = 0.10–0.22, p < 0.001). The trophic transfer of antibiotics from phytoplankton to zooplankton (BMFs) were positively correlated with both phytoplankton biomass (n = 30, R2 = 0.58, p < 0.001) and temperature (n = 132–150, R2 = 0.12–0.43, p < 0.001). Mean BMFs of ciprofloxacin, lomefloxacin, ofloxacin, oxytetracycline, and tetracycline ranged between 0.18 and 2.25, implying these chemicals can undergo biomagnification along planktonic food webs. The present research demonstrates the important role of biogeochemical and physical factors in the environmental fate of antibiotics at large spatiotemporal scales.

Tissue distribution of organic contaminants in stranded pregnant sperm whale (Physeter microcephalus) from the Huizhou coast of the South China Sea

Twelve persistent organic pollutants (POPs) were measured in 11 tissue samples from a pregnant sperm whale stranded on the Huizhou coast of the South China Sea, China, in March 2017. POPs were found to be more concentrated in the irrigated tissues such as placenta, ovary, mammary gland, and liver than the less irrigated tissues such as epidermis. High POP levels detected in the placenta might result in abnormal hormone secretion in the placenta, which would affect the unborn offspring. We hypothesized that ovary is potentially vulnerable to the exposure of higher contaminant levels. The PAH concentrations were higher in the lung than in other tissues, which suggest that PAH levels in the lung were breath-dependent in the sperm whale. The concentrations of POPs except PAHs in the sperm whale blubber were lower than those in the same species in the Northern Hemisphere and were comparable to or lower than those in the same species in the Southern Hemisphere.

Alkane and polycyclic aromatic hydrocarbons in sediments and benthic invertebrates of the northern Chukchi Sea

The Hanna Shoal region represents an important northern gateway for transport and deposition in the Chukchi Sea. This study determined the concentration and distribution of organic contaminants (aliphatic hydrocarbon and polycyclic aromatic hydrocarbons, PAHs) in surface sediments from 34 sites across Hanna Shoal. Up to 31 total PAHs, including parent and alkyl homologues were detected with total concentrations ranging from a low of 168ngg−1 the western flank of Hanna Shoal (station H34) to 1147ngg−1 at station in Barrow Canyon (station BarC5). Alkyl PAHs were more abundant than parent structures and accounted for 53–64% of the summed concentrations suggesting overall at background levels (< 1600ngg−1) in sediments. Alkane (C15–C33) hydrocarbons ranged from 4.3µgg−1 on the southern flank of Hanna shoal to 31µgg−1 at a northern station. Sediments were often dominated by short chain (C15–C22) alkanes with overall terrestrial aquatic ratios (TAR) for the region averaging 0.20. Based on the ratio of Fl/(Fl+ Py) and BaF/(Baf+BeP) verses (BA/BA+Ch) in sediments, PAHs are largely derived from petrogenic sources with minor amounts of mixed combustion sources. A diversity of PAHs were detected in the northern whelk Neptunea heros foot muscle with total concentrations ranging from 0.14 to 1.5µgg−1 dry tissue wt. Larger (and presumably older) animals showed higher levels of PAH per unit muscle tissue, suggesting that animals may bioaccumulate PAHs over time, with low but increasing concentrations also present in internal and external eggs. Alkane hydrocarbons were also higher in whelks with distributions similar to that seen in sediments. The mussel Muscularus discors collected in Barrow Canyon showed constrained distributions and substantially lower concentrations of both PAHs and alkanes than the surrounding surface sediments.

Spatial distribution of organic contaminants in three rivers of Southern England bound to suspended particulate material and dissolved in water

The spatial distribution of pharmaceuticals, personal care products (PPCPs) and other emerging contaminants (ECs) such as plasticisers, perflourinated compounds (PFCs) and illicit drug metabolites in water and bound to suspended particulate material (SPM) is not well-understood. Here, we quantify levels of thirteen selected contaminants in water (n=88) and their partition to suspended particulate material (SPM, n=16) in three previously-unstudied rivers of Greater London and Southern England during a key reproduction/spawning period. Analysis was conducted using an in-house validated method for Solid Phase Extraction followed by High-Performance Liquid Chromatography-Tandem Mass-Spectrometry. Analytes were extracted from SPM using an optimised method for ultrasonic-assisted solvent extraction. Detection frequencies of contaminants dissolved in water ranged from 3% (ethinylestradiol) to 100% (bisphenol-A). Overall mean concentrations in the aqueous-phase ranged from 14.7ng/L (benzoylecgonine) to 159ng/L (bisphenol-A). Sewage treatment works (STW) effluent was the predominant source of pharmaceuticals, while plasticisers/perfluorinated compounds may additionally enter rivers via other sources. In SPM, detection frequencies ranged from 44% (PFOA) to 94% (hydroxyacetophenone). Mean quantifiable levels of analytes bound to SPM ranged from 13.5ng/g dry SPM (0.33ng bound/L water) perfluorononanoic acid to 2830ng/g dry SPM (14.3ng bound/L water) perfluorooctanesulfonic acid. Long chain (>C7) amphipathic and acidic PFCs were found to more preferentially bind to SPM than short chain PFCs and other contaminants (Kd=34.1–75.5 vs <5 respectively). Per capita daily contributions of studied contaminants entering rivers ranged from 0.157μg/person/day of benzoylecgonine (cocaine metabolite) to 58.6μg/person/day of bisphenol-A. The large sample size of this work (n=104) enabled ANOVA followed by Tukey HSD post-hoc tests to establish significant trends in PPCP/EC spatial distribution from headwaters through downstream stretches of studied rivers. Novel findings include environmental Kd calculations, the occurrence of contaminants in river headwaters, increases in contaminant metabolite concentrations downstream of STW effluents revealing possible in-river degradation or de-conjugation, the influence of polarity and acidity in the partition of contaminants to particulate-material, among others.

Regional variability in bed-sediment concentrations of wastewater compounds, hormones and PAHs for portions of coastal New York and New Jersey impacted by hurricane Sandy

Bed sediment samples from 79 coastal New York and New Jersey, USA sites were analyzed for 75 compounds including wastewater associated contaminants, PAHs, and other organic compounds to assess the post-Hurricane Sandy distribution of organic contaminants among six regions. These results provide the first assessment of wastewater compounds, hormones, and PAHs in bed sediment for this region. Concentrations of most wastewater contaminants and PAHs were highest in the most developed region (Upper Harbor/Newark Bay, UHNB) and reflected the wastewater inputs to this area. Although the lack of pre-Hurricane Sandy data for most of these compounds make it impossible to assess the effect of the storm on wastewater contaminant concentrations, PAH concentrations in the UHNB region reflect pre-Hurricane Sandy conditions in this region. Lower hormone concentrations than predicted by the total organic carbon relation occurred in UHNB samples, suggesting that hormones are being degraded in the UHNB region.

Impact of flash flood events on the distribution of organic pollutants in surface sediments from a Mediterranean coastal lagoon (Mar Menor, SE Spain).

The influence of flash flood events on the input and distribution of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and organochlorinated pesticides (OCPs) in surface sediments from the Mar Menor lagoon were characterized in this study. These contaminants were analyzed in surface water samples collected during two flash flood events in the main surface watercourse which flow into the Mar Menor lagoon. Surface sediments were sampled semiannually before and after flash flood events. The total input of PAHs, OCPs, and PCBs (sorbed + dissolved) during two flash flood events was estimated at 0.98, 1.32, and 0.34kg, respectively, the main input corresponding to p,p'-DDE (1.00kg). The distribution of organic contaminants in surface sediments was not homogeneous as a consequence of the presence of many simultaneous sources and different meteorological, hydrodynamic, and physicochemical conditions. As a consequence of flash flood events, p,p'-DDE concentrations in surface sediments increased significantly in the central and south zones of the lagoon. However, in the case of PCBs, a dilution effect was observed in the south zone after such events, reducing the environmental risk. These changes in the pollutant distribution persisted at least 1year later (autumn 2010), showing that the impact of flood events in the distribution of persistent organic contaminants in Mediterranean coastal lagoons is of relevance according to the ecological risk assessment carried out. The impact of these events should be also considered in other coastal systems, especially in semiarid and semiconfined areas.

Effects of predicted climatic changes on distribution of organic contaminants in brackish water mesocosms

Predicted consequences of future climate change in the northern Baltic Sea include increases in sea surface temperatures and terrestrial dissolved organic carbon (DOC) runoff. These changes are expected to alter environmental distribution of anthropogenic organic contaminants (OCs). To assess likely shifts in their distributions, outdoor mesocosms were employed to mimic pelagic ecosystems at two temperatures and two DOC concentrations, current: 15°C and 4mgDOCL−1 and, within ranges of predicted increases, 18°C and 6mgDOCL−1, respectively. Selected organic contaminants were added to the mesocosms to monitor changes in their distribution induced by the treatments. OC partitioning to particulate matter and sedimentation were enhanced at the higher DOC concentration, at both temperatures, while higher losses and lower partitioning of OCs to DOC were observed at the higher temperature. No combined effects of higher temperature and DOC on partitioning were observed, possibly because of the balancing nature of these processes. Therefore, changes in OCs' fates may largely depend on whether they are most sensitive to temperature or DOC concentration rises. Bromoanilines, phenanthrene, biphenyl and naphthalene were sensitive to the rise in DOC concentration, whereas organophosphates, chlorobenzenes (PCBz) and polychlorinated biphenyls (PCBs) were more sensitive to temperature. Mitotane and diflufenican were sensitive to both temperature and DOC concentration rises individually, but not in combination.

Strategy for characterization of distribution and associations of organobromine compounds in soil using synchrotron radiation based spectromicroscopies.

It is imperative to obtain information on the binding sites and distribution of organic contaminants in soils in order to understand their reactions and fates in soils. Here we propose a novel strategy that enables in situ observation at the micrometer scale of the spatial distribution of organobromine compounds and characterization of their associations with organic carbon (OC) forms (i.e., C-functional groups) in soils. According to the strategy, two complementary synchrotron radiation-based spectroscopic techniques (i.e., Fourier transform-infrared (FT-IR) and micro X-ray fluorescence (μ-XRF) spectromicroscopies) were applied to characterize the binding sites and distribution of Br (as a conservative tracer for organobromine compounds), OC forms, clay minerals, and other mineral elements within soil particles, respectively, at a 6-10 μm-scale spatial resolution. This study is the first in situ investigation on the microscale locations of organobromine compounds at environmental levels and their associations with OC forms and clay mineral/elements in natural soils. The strategy paves the way toward in situ characterization of the distribution, speciation, and binding sites of some organic contaminants, which is critical in understanding their associated environmental processes in soils.