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1.
Matrix-bound phosphine (MBP) has been measured in sediment from two cores in Lake Illawarra on the south east coast of Australia. The sediments were also dated in the upper layers. MBP concentrations found range from 142 to 1813 ng kg−1, dw (dry weight of sediment) with some values being amongst the highest ever measured. Values of MBP in deeper sediments were higher than for near surface samples, but the patterns with depth were not consistent. Strong correlations were noted between MBP and organic phosphorus (OP, r > 0.8) and with total phosphorus (TP, r > 0.7), but only moderate correlations were found with organic carbon (OC, r > 0.5). No correlations were found between MBP concentrations and the age of the sediments. It was confirmed that high MBP concentrations are indicative of a phosphorus rich environment. The results tend to support the premise that MBP is generated by microbial attack on OP under anaerobic conditions.  相似文献   

2.
The distributions of 16 polycyclic aromatic hydrocarbons (PAHs) were determined in the aqueous phase, suspended particulate matter (SPM), sediment, and pore water of the Daliao River Estuary in Liaodong Bay, Bohai Sea (China). Total PAH concentrations ranged from 139.16 to 1717.87 ng L−1 in surface water, from 226.57 to 1404.85 ng L−1 dry weight in SPM, from 276.26 to 1606.89 ng g−1 dry weight in sediments, and from 10.20 to 47.27 μg L−1 in pore water. PAH concentrations were at relatively moderate levels in water, SPM, sediment and pore water in comparison with those reported for other estuary and marine systems around the world. Sedimentary PAH concentrations decreased offshore owing to active deposition of laterally-transported river-borne particles. PCA analysis of the possible PAH source suggested petrogenic and pyrolytic PAH inputs in the studied region.  相似文献   

3.
Estrogenic activity was determined in sediments collected from Tokyo Bay. Sampling was performed at five stations including the site near the sewage treatment plant. The most estrogenic sediment collected near the sewage treatment plant was fractionated into ten fractions using normal-phase high-performance liquid chromatography. Chemical analysis was carried out for each fraction and nonylphenol (NP, 20,700 ng g−1 dry wt) was detected at a higher concentration than estron (2.39 ng g−1 dry wt) and 17β-estradiol (<0.7 ng g−1 dry wt). Furthermore, each fraction was administered to male mummichogs (Fundulus heteroclitus), and vitellogenin (Vtg) was measured after two weeks. The induction of Vtg was observed; this estrogenic potency could be attributed to the NP content in this fraction. This is the first report to suggest that the high NP concentration in the sediments from Tokyo Bay has the potential to induce Vtg in wild fish.  相似文献   

4.
Persistent organochlorine pollutants (POPs) such as polychlorinated biphenyls (PCBs), dichlorodiphenyl trichloroethane and its metabolites (DDTs), chlordane compounds (CHLs), and hexachlorocyclohexanes (HCHs) were determined in Japanese common squid collected from the offshore waters of Korea. Liver accumulated higher levels of contaminants than mantle. The sums of DDTs, PCBs, CHLs and HCHs in liver were in the ranges of 164-4430 ng g−1, 95-1030 ng g−1, 15-121 ng g−1, and 13-98 ng g−1 on a lipid weight basis, respectively. Among the POPs, DDTs showed distinct regional difference in concentration levels and composition between the western and eastern offshore of Korea. One of the highest concentrations of DDTs so far recorded in the western offshore of Korea, that is Yellow Sea. This implies ongoing fresh input of technical DDT to this regional sea. HCHs were relatively high in the Yellow Sea as well, with an enhanced signal of γ-HCH indicating recent input of lindane. In contrast, CHLs showed higher level in the eastern offshore of Korea, that is East Sea, but PCBs showed an even distribution in both regions. Squid could be a useful bio-indicator for monitoring offshore water contamination by POPs.  相似文献   

5.
Perfluorinated chemicals including PFOA and PFOS have been widely used in consumer products and have become ubiquitous pollutants widely distributed in the aqueous environment. Following a major flood event in 2011, water samples were collected along a spatial gradient of the Brisbane River system to provide an initial estimate of the release of PFASs from flooded urban areas. PFOA (mean concentrations 0.13–6.1 ng L−1) and PFOS (mean concentrations 0.18–15 ng L−1) were the most frequently detected and abundant PFASs. Mean total PFASs concentrations increased from 0.83 ng L−1 at the upstream Wivenhoe Dam to 40 ng L−1 at Oxley Creek, representing an urban catchment. Total masses of PFOA and PFOS delivered into Moreton Bay from January to March were estimated to be 5.6 kg and 12 kg respectively. From this study, urban floodwaters appear to be a previously overlooked source of PFASs into the surrounding environment.  相似文献   

6.
Spatial variations in the sinking export of organic material were assessed within the Hudson Bay system (i.e., Hudson Bay, Hudson Strait and Foxe Basin) during the second oceanographic expedition of ArcticNet, on board the CCGS Amundsen in early fall 2005. Sinking fluxes of particulate organic material were measured using short-term free-drifting particle interceptor traps deployed at 50, 100 and 150 m for 8–20 h at eight stations. Measurements of chlorophyll a (chl a), pheopigments (pheo), particulate organic carbon (POC), biogenic silica (BioSi), protists, fecal pellets and bacteria were performed on the collected material. In parallel, sea surface salinity and temperature were determined at 121 stations in the Hudson Bay system. Three hydrographic regions presenting different sedimentation patterns were identified based on average surface salinity and temperature. Hudson Strait was characterized by a marine signature, with high salinity (average=32.3) and low temperature (average=2.1 °C). Eastern Hudson Bay was strongly influenced by river runoff and showed the lowest average salinity (26.6) and highest average temperature (7.6 °C) of the three regions. Western Hudson Bay showed intermediate salinity (average=29.4) and temperature (average=4.4 °C). Sinking fluxes of total pigments (chl a+pheo: 3.37 mg m−2 d−1), diatom-associated carbon (19.8 mg m−2 d−1) and BioSi (50.2 mg m−2 d−1) at 50 m were highest in Hudson Strait. Eastern Hudson Bay showed higher sinking fluxes of total pigments (0.52 mg m−2 d−1), diatom-associated carbon (3.29 mg m−2 d−1) and BioSi (36.6 mg m−2 d−1) compared to western Hudson Bay (0.19, 0.05 and 7.76 mg m−2 d−1, respectively). POC sinking fluxes at 50 m were low and relatively uniform throughout the Hudson Bay system (50.0–76.8 mg C m−2 d−1), but spatial variations in the composition of the sinking organic material were observed. A large part (37–78%) of the total sinking POC was unidentifiable by microscopic observation and was qualified as amorphous detritus. Considering only the identifiable material, the major contributors to the POC sinking flux were intact protist cells in Hudson Strait (28%), fecal pellets in eastern Hudson Bay (52%) and bacteria in western Hudson Bay (17%). A significant depth-related attenuation of the POC sinking fluxes (average loss between 50 and 150 m=32%) and a significant increase in the BioSi:POC ratio (average increase between 50 and 150 m=76%) were observed in Hudson Strait and eastern Hudson Bay. For all other sinking fluxes and composition ratios, we found no statistically significant difference with depth. These results show that during fall, the sinking export of total POC from the euphotic zone remained fairly constant throughout the Hudson Bay system, whereas other components of the organic sinking material (e.g., chl a, BioSi, fecal pellets, protist cells) showed strong spatial variations.  相似文献   

7.
The study aimed to determine the spatial distribution of n-alkanes and polycyclic aromatic hydrocarbons (PAHs) in surface sediments of the Segara Anakan nature reserve and their potential origins using gas chromatography–mass spectrometry. Total alkane concentrations ranged from 3755 to 129,027 μg kg−1, and the concentrations of 16 PAHs ranged from 375 to 29,517 μg kg−1. The ratios of specific n-alkanes (e.g., CPI24–34, WaxCn, and Paq), including a new proposed index, terrestrial–marine discriminant (TMD), as well as the ratios of selected PAHs (e.g., Ant/∑178, Fl/∑202, BaAnt/∑228, and IPyr/∑276), showed that the sources of hydrocarbons in the sediments were generally biogenic, including both terrigenous and marine, with an anthropogenic pyrolytic contribution (petrogenic and biogenic combustion). For the environmental risk assessment, a sediment quality guideline (SQGs) comparison indicated that the station risk levels ranged from low to medium-low, except for R6, which has a greater impact on the ecological risk for marine organisms.  相似文献   

8.
The Changjiang has transported large quantities of polycyclic aromatic hydrocarbons (PAHs) to the East China Sea (ECS), but information of these pollutants in zooplankton is limited. To understand PAHs pollution in zooplankton in the ECS, total concentrations of PAHs in zooplankton from surface waters were measured. Values of PAHs ranged from 2 to 3500 ng m−3 in the ECS, with highest PAHs levels located at the salinity front between the Changjiang Diluted Water (CDW) and the mid-shelf waters. In contrast, concentrations of zooplankton PAHs in the mid-shelf and outer-shelf waters were significantly lower (2–23 ng m−3) than those in the CDW. These results demonstrate that PAHs are conspicuously accumulated in zooplankton at the salinity front between the CDW and the mid-shelf waters. These higher levels of PAHs in zooplankton at the salinity front may be further biomagnified in marine organisms of higher trophic levels through their feeding activities.  相似文献   

9.
The anti-microbial agent triclosan (TCS), and its derivative methyl-triclosan (Me-TCS), are discharged with treated effluents from wastewater treatment plants to receiving environments. We investigated the bioconcentration of TCS and Me-TCS in mussels (Mytilus galloprovincialis) exposed to TCS (100 ng L−1) for 30 days in seawater aquaria (19 ± 2 °C) with fresh phytoplankton as a food source. Bioconcentration increased with time reaching a steady-state around 24–30 days. The bioconcentration factor (log BCF) for TCS were 2.81 L kg−1 (dry weight) and 4.13 L kg−1, when lipid normalised concentrations were used. Mussels were also deployed in cages at four marine locations receiving effluents from WWTPs. The mean (±SD) TCS and Me-TCS concentrations for mussels from these sites were 9.87 (±1.34) and 6.99 (±2.44) μg kg−1. The study showed that mussels can be a useful tool for monitoring pollution of TCS and Me-TCS in marine and estuarine environments.  相似文献   

10.
The concentrations of 21 polybrominated diphenyl ethers (PBDEs) congeners were analyzed in organisms within a marine food web collected from the Liaodong Bay, North China. The total concentrations of PBDEs in all samples ranged from 0.87 to 91.4 ng g−1 lipid weight (lw). BDE-47 was the predominant congener and had a concentration ranging from 0.30 to 36.1 ng g−1 lw. The trophic magnification factors (TMF) of the PBDEs were calculated using the trophic levels obtained from the stable nitrogen isotope ratios. The TMF value of ∑PBDEs was 3.50 for the entire food web and 2.21 for the food web excluding seabirds. Four concentration ratios, BDE-99/BDE-100, BDE-99/BDE-47, BDE-153/BDE-154 and BDE-183/BDE-154, decreased linearly with the increase of the trophic levels in the invertebrates and the fishes (p < 0.01). The results suggested that the PBDEs were steadily metabolized in the trophic transfer process along the food chain.  相似文献   

11.
The distribution and bioaccumulation features of PCBs, DDTs, and HCHs were investigated in the sediments and Manila clams collected from along the Mid-Western coast of Korea. The measured concentrations of ΣPCBs, ΣDDTs and ΣHCHs were 1.08–3.5, 0.12–0.35 and 0.090–0.30 ng g−1 dw in sediment, and 33–390, 7.4–46 and 6.3–27 ng g−1 lipid in Manila clam, respectively. Their levels were found to be relatively lower than those of other contaminated areas and the consumption of Manila clam from these areas seems to be safe for human health according to calculated lifetime cancer risk and hazard indices. The ΣPCBs and ΣDDTs concentrations in sediments showed a significant relationship to those in clams. The significant correlation was observed between BSAF in clams and Kow for each PCB congeners and DDT metabolites. These findings support that the PCBs and DDTs levels, which are highly hydrophobic chemicals, in clam reflect the sediment pollution through bioaccumulation.  相似文献   

12.
In this study, total metal (Al, Fe, Mn and Cu) and PAHs analyses have been done in the surface sediments. Sediment samples have been collected from seven parts of the Marmara Sea and the coast of Istanbul during 2009. Total Al, Fe, Mn and Cu contents vary between 1.8% and 5.4%; 1.1% and 2.8%; 122 and 259 μg g−1; 27 and 416 μg g−1, respectively. EF and CF values of Fe and Mn are lower than 1.5 and 1, respectively, in all the stations. Total PAH contents range between 135 and 6009 ng g−1 in the surface sediments. The origin of PAHs has been found pyrolitic according to the Phe/Ant ratio in the all stations. Contrastingly, at K0, MKC and MY1 Stations, PAH origins have been observed petrogenic according to the Flu/Pyr ratio.  相似文献   

13.
The first analyses of PAHs in marine sediments within Rijeka Bay started in 1998 at three sampling sites offshore from the petroleum refinery facilities and were extended in 1999 to three more sampling points in front of the repair shipyard within the same east industrial zone. The small Svezanj cove, lying between the shipyard and the petroleum refinery was chosen as the reference point. The concentrations of PAHs were considerably higher in the shipyard environment (average: 3009-6314 μg kg−1 d.w.) in comparison to the petroleum refinery area (average: 279-919 μg kg−1 d.w.), while the PAHs load at reference point was close to the latter level (average: 717 μg kg−1 d.w.). The Phe/Anth and Flo/Py ratios indicate the dominant pyrogenic sources, except for the results from 1999 to 2000 with dominant petrogenic origin at some sites. A declining trend of total PAHs, and consequently toxicity indices was observed at all sites.  相似文献   

14.
This study investigated the concentrations and distribution of Perfluoroalkyl and polyfluoroalkyl substances (PFAS) in sediments of 12 rivers from South Bohai coastal watersheds. The highest concentrations of ΣPFAS (31.920 ng g−1 dw) and PFOA (29.021 ng g−1 dw) were found in sediments from the Xiaoqing River, which was indicative of local point sources in this region. As for other rivers, concentrations of ΣPFAS ranged from 0.218 to 1.583 ng g−1 dw were found in the coastal sediments and from 0.167 to 1.953 ng g−1 dw in the riverine sediments. Predominant PFAS from coastal and riverine areas were PFOA and PFBS, with percentages of 30% and 35%, respectively. Partitioning analysis showed the concentrations of PFNA, PFDA and PFHxS were significantly correlated with organic carbon. The results of a preliminary environmental hazard assessment showed that PFOS posed the highest hazard in the Mi River, while PFOA posed a relative higher hazard in the Xiaoqing River.  相似文献   

15.
The ongoing regression of sea ice cover is expected to significantly affect the fate of organic carbon over the Arctic continental shelves. Long-term moored sediment traps were deployed in 2005–2006 in the Beaufort Sea, Northern Baffin Bay and the Laptev Sea to compare the annual variability of POC fluxes and to evaluate the factors regulating the annual cycle of carbon export over these continental shelves. Annual POC fluxes at 200 m ranged from 1.6 to 5.9 g C m−2 yr−1 with the highest export in Northern Baffin Bay and the lowest export over the Mackenzie Shelf in the Beaufort Sea. Each annual cycle exhibited an increase in POC export a few weeks before, during, or immediately following sea ice melt, but showed different patterns over the remainder of the cycle. Enhanced primary production, discharge of the Lena River, and resuspension events contributed to periods of elevated POC export over the Laptev Sea slope. High POC fluxes in Northern Baffin Bay reflected periods of elevated primary production in the North Water polynya. In the Beaufort Sea sediment resuspension contributed to most of the large export events. Our results suggest that the outer shelf of the Laptev Sea will likely sustain the largest increase in POC export in the next few years due to the large reduction in ice cover and the possible increase in the Lena River discharge. The large differences in forcing among the regions investigated reinforce the importance of monitoring POC fluxes in the different oceanographic regimes that characterize the Arctic shelves to assess the response of the Arctic Ocean carbon cycle to interannual variability and climate change.  相似文献   

16.
We observed a phytoplankton bloom downstream of a large estuarine plume induced by heavy precipitation during a cruise conducted in the Pearl River estuary and the northern South China Sea in May–June 2001. The plume delivered a significant amount of nutrients into the estuary and the adjacent coastal region, and enhanced stratification stimulating a phytoplankton bloom in the region near and offshore of Hong Kong. A several fold increase (0.2–1.8 μg Chl L−1) in biomass (Chl a) was observed during the bloom. During the bloom event, the surface water phytoplankton community structure significantly shifted from a pico-phytoplankton dominated community to one dominated by micro-phytoplankton (>20 μm). In addition to increased Chl a, we observed a significant drawdown of pCO2, biological uptake of dissolved inorganic carbon (DIC) and an associated enhancement of dissolved oxygen and pH, demonstrating enhanced photosynthesis during the bloom. During the bloom, we estimated a net DIC drawdown of 100–150 μmol kg−1 and a TAlk increase of 0–50 μmol kg−1. The mean sea–air CO2 flux at the peak of the bloom was estimated to be as high as ∼−18 mmol m−2 d−1. For an average surface water depth of 5 m, a very high apparent biological CO2 consumption rate of 70–110 mmol m−2 d−1 was estimated. This value is 2–6 times higher than the estimated air–sea exchange rate.  相似文献   

17.
The present work aimed at studying the origin of particulate organic matter in Guanabara Bay and in some rivers of the Guanabara basin by using elemental composition, isotopic ratios (δ13C and δ15N) and molecular markers (sterols) in samples collected in two periods (winter and summer). Elemental and isotopic compositions were determined by dry combustion and mass spectrometry, respectively, while sterols were investigated by GC–FID and GC–MS. Higher sterol concentrations were present in the north-western part of the bay in winter (5.10–23.5 μg L–1). The high abundance of algal sterols (26–57% of total sterols), the elemental composition (C/N=6–8) and the isotopic signatures (δ13C=−21.3‰ to −15.1‰ and δ15N=+7.3‰ to +11.1‰) suggested the predominance of autochthonous organic matter, as expected for an eutrophic bay, although seasonal variation in phytoplankton activity was observed. Coprostanol concentration (fecal sterol) was at least one order of magnitude higher in the particulate material from fluvial samples (4.65–55.98 μg L–1) than in the bay waters (<0.33 μg L–1). This could be ascribed to a combination of factors including efficient particle removal to sediments in the estuarine transition zone, dilution with bay water and bacterial degradation during particle transport in the water column.  相似文献   

18.
Mobilisation of sedimentary monosulfidic black ooze (MBO) may result in rapid deoxygenation and acidification of surface waters, and release of potentially toxic metals. This study examines the extent and nature of MBO accumulation in the Geographe Bay area, Western Australia. MBO accumulations were found to be widespread in benthic sediments of the Geographe Bay area with acid-volatile sulfide (AVS) contents as high as 320 μmol g−1. The MBO materials often had unusually high dissolved sulfide (S−II) concentrations in their pore-waters (up to 610 mg L−1) and elevated elemental sulfur (S0) contents (up to 51 μmol g−1). Dissolved S−II is able to accumulate due to limited iron availability and S0 is largely its partial oxidation product. The availability of organic carbon and Fe limited MBO accumulation at many sites. A comparison of AVS and simultaneously extracted metal (SEM) concentrations has shown that metals are likely to be bound in sulfide complexes.  相似文献   

19.
The North-East Atlantic porbeagle (Lamna nasus) population has declined dramatically over the last few decades and is currently classified as ‘Critically Endangered’. As long-lived, apex predators, they may be vulnerable to bioaccumulation of contaminants. In this study organohalogen compounds and trace elements were analysed in 12 specimens caught as incidental bycatch in commercial gillnet fisheries in the Celtic Sea in 2011. Levels of organohalogen contaminants were low or undetectable (summed CB and BDE concentrations 0.04–0.85 mg kg−1 wet weight). A notably high Cd concentration (7.2 mg kg−1 wet weight) was observed in one mature male, whereas the range observed in the other samples was much lower (0.04–0.26 mg kg−1 wet weight). Hg and Pb concentrations were detected only in single animals, at 0.34 and 0.08 mg kg−1 wet weight, respectively. These contaminant levels were low in comparison to other published studies for shark species.  相似文献   

20.
The air–sea ice CO2 flux was measured over landfast sea ice in the Chukchi Sea, off Barrow, Alaska in late May 2008 with a chamber technique. The ice cover transitioned from a cold early spring to a warm late spring state, with an increase in air temperature and incipient surface melt. During melt, brine salinity and brine dissolved inorganic carbon concentration (DIC) decreased from 67.3 to 18.7 and 3977.6 to 1163.5 μmol kg−1, respectively. In contrast, the salinity and DIC of under-ice water at depths of 3 and 5 m below the ice surface remained almost constant with average values of 32.4±0.3 (standard deviation) and 2163.1±16.8 μmol kg−1, respectively. The air–sea ice CO2 flux decreased from +0.7 to −1.0 mmol m−2 day−1 (where a positive value indicates CO2 being released to the atmosphere from the ice surface). During this early to late spring transition, brought on by surface melt, sea ice shifted from a source to a sink for atmospheric CO2, with a rapid decrease of brine DIC likely associated with a decrease in the partial pressure of CO2 of brine from a supersaturated to an undersaturated state compared to the atmosphere. Formation of superimposed ice coincident with melt was not sufficient to shut down ice–air gas exchange.  相似文献   

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