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1.
Poly- and perfluorinated alkyl substances (PFASs) are groups of persistent toxic substances that have been commonly detected in wastewater treatment plants (WWTPs). In some cases, the activated sludge (AS) in WWTPs will encounter special wastewaters containing PFASs up to tens of milligram per liter (mg L?1). However, under this condition, the potential impacts of PFASs on AS process remain unclear. In the present research, a lab-scale sequencing batch reactor was continuously exposed to perfluorooctanoic acid (PFOA), used as a representation for PFASs, at 20 mg L?1 to mimic the extreme condition. The objective is to explore the impact of PFOA on AS process in terms of its wastewater treatment performance and evolution of microbial communities. The results indicate that PFOA restrained the microbial growth and affected the dissolved organic carbon removal. These negative impacts could be recovered after long-term adaptation. Besides, 20 mg L?1 PFOA shows limited inhibition on nitrification and denitrification, suggesting a safe exposure level of PFOA for nitrogen removal. For microbial evolution, PFOA induced changes of communities during long-term exposure. The high abundance of Bacteroidetes, Proteobacteria, and Acidobacteria maintained over time reveals their tolerance towards PFOA. The occurrences of PFOA-resistant species are also observed. The present research provides new insight into the possible impacts of typical PFAS at high concentrations on AS process.  相似文献   

2.
This study presents concentrations of perfluorinated compounds in food and the dietary intake of perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) in The Netherlands. The concentrations of perfluorinated compounds in food were analyzed in pooled samples of foodstuffs randomly purchased in several Dutch retail store chains with nation-wide coverage. The concentrations analyzed for PFOS and PFOA were used to assess the exposure to these compounds in The Netherlands. As concentrations in drinking water in The Netherlands were missing for these compounds, conservative default concentrations of 7 pg/g for PFOS and 9 pg/g for PFOA, as reported by European Food Safety Authority, were used in the exposure assessment. In food, 6 out of 14 analyzed perfluorinated compounds could be quantified in the majority of the food categories (perfluoroheptanoic acid (PFHpA), PFOA, perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), perfluoro-1-hexanesulfonate (PFHxS), and PFOS). The highest concentration of the sum of these six compounds was found in crustaceans (825 pg/g product, PFOS: 582 pg/g product) and in lean fish (481 pg/g product, PFOS: 308 pg/g product). Lower concentrations were found in beef, fatty fish, flour, butter, eggs, and cheese (concentrations between 20 and 100 pg/g product; PFOS, 29-82 pg/g product) and milk, pork, bakery products, chicken, vegetable, and industrial oils (concentration lower than 10 pg/g product; PFOS not detected). The median long-term intake for PFOS was 0.3 ng/kg bw/day and for PFOA 0.2 ng/kg bw/day. The corresponding high level intakes (99th percentile) were 0.6 and 0.5 ng/kg bw/day, respectively. These intakes were well below the tolerable daily intake values of both compounds (PFOS, 150 ng/kg bw/day; PFOA, 1500 ng/kg bw/day). The intake calculations quantified the contribution of drinking water to the PFOS and PFOA intake in The Netherlands. Important contributors of PFOA intake were vegetables/fruit and flour. Milk, beef, and lean fish were important contributors of PFOS intake.  相似文献   

3.
The aim of this study was to determine the dietary intake of perfluorinated chemicals (PFCs) by the population of Tarragona County (Catalonia, Spain). PFC levels were determined in 36 composite samples of foodstuffs randomly purchased in various locations. Exposure to PFCs through the diet was estimated for various age/gender groups. Perfluorooctane sulfonate (PFOS), perfluorocarboxylate perfluorooctanoate (PFOA), and perfluoroheptanoic acid (PFHpA) were the only detected PFCs in foodstuffs. On average, for a standard adult man (70 kg of body weight), the dietary intake of PFOS was estimated to be 62.5 or 74.2 ng/day (assuming ND=0 or ND=1/2 LOD, respectively). Fish, followed by dairy products and meats, were the main contributors to PFOS intake. For an adult man, the intake of PFOS (1.07 ng/kg/day) and those of PFOA and PFHpA were lower than that recently reported for Canada (4.0 ng/kg/day), and considerably lower than that previously found in the United Kingdom, the only two countries where, to date, results concerning this issue have been reported. A correlation between dietary intake and blood levels of PFOS is suggested. However, the current results do not justify dietary intake as the main route of exposure governing blood concentrations of other PFCs.  相似文献   

4.
A vegetation study was carried out to investigate the carryover of Perfluorooctanoic Acid (PFOA) and Perfluorooctane Sulfonate (PFOS) from soil mixed with contaminated sewage sludge to potato, carrot, and cucumber plants. Analysis was done by liquid-extraction using acetonitrile with dispersive SPE cleanup and subsequent HPLC-MS/MS. In order to assess the transfer potential from soil, transfer factors (TF) were calculated for the different plant compartments: TF = [PFC](plant (wet substance))/[PFC](soil (dry weight)). The highest TF were found for the vegetative plant compartments with average values for PFOS below those for PFOA: cucumber, 0.17 (PFOS), 0.88 (PFOA); potato, 0.36 (PFOS), 0.40 (PFOA); carrot, 0.38 (PFOS), 0.53 (PFOA). Transfer of PFOA and PFOS into potato peelings (average values of TF: PFOA 0.03, PFOS 0.04) exceeded the carryover to the peeled tubers (PFOA 0.01, PFOS < 0.01). In carrots, this difference did not occur (average values of TF: PFOA 0.04, PFOS 0.04). Transfer of PFOS into the unpeeled cucumbers was low and comparable to that of peeled potatoes (TF < 0.01). For PFOA, it was higher (TF: 0.03).  相似文献   

5.
Comprehensive survey of major rivers in the Tokyo metropolitan area was conducted for clarifying the emission sources of perfluorooctane sulfonate (PFOS) in Tokyo. PFOS was found at all sampling sites at concentrations ranging from 0.5 to 58 ng L?1; in addition to this, it was also indicated that unknown PFOS emission sources are present in the midstream of the Tama River basin. The relationship between PFOS and perfluorooctanoic acid (PFOA) was constant at a ratio of 10:3 (PFOS/PFOA) throughout the Tama River basin. The sum of daily load amounts of PFOS from Tokyo’s major rivers to Tokyo Bay reached 215 g day?1. This value corresponds to 12.8 μg day?1 per person using the sum of wastewater treatment district populations. In contrast, an estimation of PFOS contribution of domestic wastewater was also attempted, and the contribution was 1.6 μg day?1 per person. We took samples up trunk sewers in the Tama River and finally found at the highest PFOS concentration (58,000 ng L?1) from one of the wastewater of the electronic parts manufacturing facilities.  相似文献   

6.
In this study, the concentrations of 15 perfluorinated compounds (PFCs) were analyzed in 30 water samples collected in Catalonia (Spain) at three stages of the drinking water treatment process in several water purification plants. In addition, the concentrations of 13 PFCs were determined in samples of fish and shellfish collected from coastal areas of Catalonia. The intake of PFCs through both pathways, drinking water intake and fish and shellfish consumption, was also estimated. In water samples, the highest mean concentrations corresponded to perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) (1.81 and 2.40 ng/L, respectively), whereas perfluorodecanosulfonate (PFDS) and perfluorotetradecanoic acid (PFTDA) were under their respective limits of detection in all analyzed samples. The results show that although the current treatment processes caused slight reductions in PFC concentrations, these processes did not mean significant changes in the amounts of PFCs already contained in the raw water. Among the analyzed PFCs in fish and shellfish, only seven compounds could be detected in at least one composite sample. PFOS showed the highest mean concentration (2.70 ng/g fw), being detected in all species with the exception of mussels. With regard to PFOA (mean, 0.074 ng/g fw), the highest concentrations were detected in prawn and hake (0.098 and 0.091 ng/g fw, respectively). The current exposure to PFCs through consumption of fish and shellfish indicates that it should not be of concern for the consumers. The amounts ingested are well below the recommended tolerable daily intakes, at least for those PFCs for which information is available.  相似文献   

7.
Despite the growing public interest in perfluorinated compounds (PFCs), very few studies have reported the sources and pathways of human exposure to these compounds in China. In this study, concentrations of 10 PFCs were measured in human blood, water (tap water and surface water), freshwater fish, and seafood samples collected from China. On the basis of the data, we calculated daily intakes of PFCs, regional differences in human exposures, and potential risks associated with ingestion of PFCs from diet, drinking water, and indoor dust for the Chinese population. Perfluorooctane sulfonate (PFOS) was the most predominant PFC found with a mean concentration of 12.5 ng/mL in human blood from Tianjin and 0.92 ng/g wet wt in freshwater fish and seafood; perfluorooctanoic acid (PFOA) was the major PFC found in drinking water at a concentration range of 0.10 to 0.92 ng/L. The estimated daily intake of PFOS and PFOA via fish and seafood consumption (EDI(fish&seafood)) ranged from 0.10 to 2.51 and 0.13 to 0.38 ng/kg bw/day, respectively, for different age groups (i.e., toddlers, adolescents and children, and adults) from selected locations (i.e., Tianjin, Nanchang, Wuhan, and Shenyang). The EDI(fish&seafood) of PFCs decreased (p < 0.05) with age. The estimated daily intake of PFOS and PFOA via drinking water consumption (EDI(drinking water)) ranged from 0.006 to 0.014 and 0.010 to 0.159 ng/kg bw/day, respectively. Comparison of EDI(fish&seafood) and EDI(drinking water) values with those of the modeled total dietary intake (TDI) of PFCs by adults from Tianjin, Nanchang, Wuhan, and Shenyang showed that contributions of fish and seafood to TDI of PFOS varied depending on the location. Fish and seafood accounted for 7%, 24%, 80%, and 84% of PFOS intake in Nanchang, Shenyang, Wuhan, and Tianjin, respectively, suggesting regional differences in human exposure to PFOS. Drinking water was a minor source of PFOS (<1%) exposure in adults from all the study locations.  相似文献   

8.
Human exposure to perfluorinated compounds is a worldwide phenomenon; however, routes of human exposure to these compounds have not been well-characterized. Fifty-four solid food composite samples collected as part of the Canadian Total Diet Study (TDS) were analyzed for perfluorocarboxylates and perfluorooctanesulfonate (PFOS) using a methanol extraction liquid chromatography tandem mass spectrometry method. Foods analyzed included fish and seafood, meat, poultry, frozen entrées, fast food, and microwave popcorn collected from 1992 to 2004 and prepared as for consumption. Nine composites contained detectable levels of perfluorinated compounds-four meat-containing, three fish and shellfish, one fast food, and one microwave popcorn. PFOS and perfluorooctanoate (PFOA) were detected the most frequently; concentrations ranged from 0.5 to 4.5 ng/g. The average dietary intake of total perfluorocarboxylates and PFOS for Canadians was estimated to be 250 ng/day, using results from the 2004 TDS composites. A comparison with intakes of perfluorocarboxylates and PFOS via other routes (air, water, dust, treated carpeting, and apparel) suggested that diet is an important source of these compounds. There was a substantial margin of exposure between the toxicological points of reference and the magnitude of dietary intake of perfluorinated compounds for Canadians >/= 12 years old.  相似文献   

9.
Perfluorooctane sulfonate (PFOS), which has numerous uses besides being an ingredient in the formulation of aqueous film-forming foams, is considered as an emerging pollutant of increasing public health and environmental concern due to recent reports of its worldwide distribution, environmental persistence and bioaccumulation potential. In an attempt to recommend a ‘risk-based’ remediation strategy, this study investigates the removal of PFOS from impacted waters and fixation of PFOS in impacted soils using a novel modified clay adsorbent (MatCARE?, patent number 2009905953). Batch adsorption tests demonstrated a much faster adsorption kinetics (only 60 min to reach equilibrium) and remarkably higher PFOS adsorption capacity (0.09 mmol g?1) of the MatCARE? compared to a commercial activated carbon (0.07 mmol g?1). Treatability studies, performed by treating the PFOS-contaminated soils with the MatCARE? (10 % w/w) and then incubating at 25 and 37 °C temperatures maintaining 60 % of the maximum water holding capacity of the soils for a period of a year, demonstrated a negligible release (water extractable) of the contaminant (only 0.5 to 0.6 %). The fixation of PFOS in soils by the new adsorbent was exothermic in nature. Soils with higher clay and organic matter content, but lower pH values, retained PFOS to a much greater extent. A cost analyses confirmed that the MatCARETM could be an economically viable option for the ‘risk-based’ remediation of PFOS in contaminated waters and soils.  相似文献   

10.
This paper describes the presence of 33 pharmaceuticals and hormones in waters from two sewage treatment plants (STPs) situated in Catalonia, in northeastern Spain. The target compounds were one psychoactive stimulant, one antiepileptic, four analgesics and non-steroidal anti-inflammatories, one lipid regulators, two anti-ulcer agents, nine antibiotics (sulfonamides and macrolides), two beta-blockers, two metabolites, and 11 hormones (free and conjugates). The determination was performed using liquid chromatography coupled to tandem mass spectrometry after enrichment by solid-phase extraction with Oasis HLB sorbent. Most of the pharmaceuticals were found in both influent and effluent samples from the two STPs. The most frequently detected were caffeine, acetaminophen, carbamazepine, diclofenac, ibuprofen, naproxen, sulfamethoxazole, sulfapyridine, sulfathiazole, ranitidine, omeprazole, estrone 3-sulfate, and estradiol 17-glucuronide. Specifically, the highest concentrations found in influents were 19,850?ng/L (acetaminophen), 9,945?ng/L (caffeine), 4,215?ng/L (ibuprofen), 5,695?ng/L (sulfamethoxazole), and 5,140?ng/L (sulfathiazole). Most of the pharmaceuticals present in influent waters were found in effluents at lower concentrations. The highest concentrations in effluents were 970?ng/L (caffeine), 670?ng/L (sulfamethoxazole), 510?ng/L (bezafibrate), and 1,032?ng/L (diclofenac).  相似文献   

11.
Atmospheric polychlorinated bihenyls (PCBs) deposit by dry and wet deposition mechanisms, and therefore they constitute a significant polluting source for lands and surface waters. Various samplers have been used to determine the PCB pollution level resulting from deposition. In the presented study, a modified wet deposition sampler (WDS) was used for sampling both wet and dry deposition samples with the same instrument by which wet deposition reservoir of the WDS is opened and dry deposition reservoir is closed when rain starts. Wet and dry deposition samples were collected between June 2008 and June 2009. In the samples taken from BUTAL which is known as an urban area with heavy traffic, ??PCB dry deposition fluxes were determined as 18?±?10 ng/m2??day, and wet deposition fluxes for dissolved and particle phase were measured as 480?±?1,185 and 475?±?1,000 ng/m2??day, respectively. The dissolved and particle-phase PCB concentrations in rain were 10?±?13 and 13?±?14 ng/l, respectively. The contribution of wet deposition to total PCB deposition was determined as 52%. PCB concentrations in the ambient air were measured to be 370?±?200 and 20?±?20 pg/m3 for gas and particle phases, respectively. Washout ratio was determined by proportioning rain concentration to concentration in air. The washout ratios of the samples were between 1,675?C311,800 and 12,775?C2,511,120 for dissolved and particulate phases, respectively.  相似文献   

12.
The article describes a novel analytical method based on solid-phase extraction and LC-MS/MS for detection of a high number (n?=?44) of selected pharmaceuticals in surface waters. The validated method showed suitable accuracy, precision, and linearity. The extraction efficiency for pharmaceuticals was mostly above 90% and the determined LOQs were generally below 5 ng/L and even down to 0.03 ng/L. The matrix effect was successfully minimized with isotopically labeled internal standards. Six river and lake samples from Slovene regions were afterwards analyzed. Forty-two of the 44 target pharmaceuticals were detected in at least two water samples; 66% of them were detected in all samples. Three analytes were present above the LOQ in all samples: caffeine (1.1–3.1 ng/L), irbesartan (0.2–9.3 ng/L), and valsartan (0.8–47 ng/L). The highest concentration was measured for valsartan. Comprehensive comparison with the literature data showed that the found concentrations of pharmaceuticals were notably lower in our study and that a number of the pharmaceuticals had not been reported previously. Comparison of the measured and predicted (calculated) environmental concentrations of pharmaceuticals in surface waters showed high discrepancy between the two approaches, clearly indicating the need for comprehensive analytical methods for routine monitoring of these newly emerging pollutants. In conclusion, our method was proven to be adequately sensitive to reliably quantify the majority of pharmaceutical contaminants even though they were found in notably lower concentrations in Slovenian surface waters than it was predicted from their consumption and from the literature.  相似文献   

13.
The impact of regular application of sewage sludge or farmyard manure on the organic contaminant loads in soil was assessed in a model rhizobox experiment. Two soils originating from a long-term field crop rotation and fertilizer experiment running since 1996 were used. The total polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons (PAHs), organochlorinated pesticides (OCPs), polybrominated diphenyl ethers (PBDEs), perfluorooctanoic acid (PFOA), and perfluorooctane sulfonate (PFOS) contents were determined in the rhizosphere and bulk soil. The results showed low but still detectable contents of PCBs and OCPs in the soil, substances which were banned a few decades ago. Among the OCPs, dichlorodiphenyltrichloroethane (DDT) and its metabolites reaching up to 18.2 µg kg?1 of the soil even exceeded the preventive levels for these compounds in agricultural soils, i.e. 7.5 µg kg?1 of soil. For PBDEs, PFOA, and PFOS, their contents in the soil significantly increased with sewage sludge application. The enhancement of the potential biodegradability of the POPs in the rhizosphere was confirmed only for hexachlorocyclohexane (γ-HCH), where, the level of γ-HCH increased significantly in the rhizosphere soil compared to bulk soil. Thus, natural attenuation of POPs in the soil-plant system seems to be insufficient for most of the investigated compounds.  相似文献   

14.
The selection of control measures for reducing metal contamination in rivers has targeted point sources such as wastewater treatment plants (WWTPs) and industrial discharges without a proper evaluation of their relative contribution to metal loads at the catchment level. The necessity of controlling pollutant inputs in a sound and cost-effective way to prevent the deterioration of chemical and ecological quality of receiving waters has highlighted the need for appropriate source assessment. As metals in rivers emanate from a wide range of sources, it is necessary to understand their relative contribution in order to reduce effectively the concentrations in receiving waters. This study presents a simple method for calculating the relative contribution of WWTPs to levels of metals in receiving waters as applied to the Aire?CCalder catchment in the UK. In this catchment, the apportionments to WWTP effluents of metal levels in rivers were 37, 31, 36 and 60?% of total cadmium (Cd), lead (Pb), mercury (Hg) and nickel (Ni), respectively. Spatial metal distribution in rivers with maximum concentrations of 0.47???g?L?1 for Cd, 8.54???g?L?1 for Pb, 0.05???g?L?1 for Hg and 10.17???g?L?1 for Ni caused by the discharge of WWTP effluents was estimated. The findings demonstrate that the proposed approach using quantification of metal loads and estimation of concentrations in receiving waters could adequately calculate the relative contribution of WWTP effluents to metal levels in receiving waters. Applications to various river catchments using site-specific data would further validate the effectiveness of the approach proposed.  相似文献   

15.
Fluorescent dissolved organic matters (FDOM) in the groundwater-river-lake environments were investigated using three-dimensional excitation-emission matrix (EEM) and measuring the dissolved organic carbon (DOC), inorganic anions and electric conductivity (EC) in shallow groundwater, river and lake waters. DOC concentrations were high and largely varied in groundwater, 16–328 μM C (mean 109?±?88 μM C), and in river waters, 43–271 μM C (mean 158?±?62 μM C) and were very low in the lake Biwa waters, 89–97 μM C (mean 93?±?2 μM C). The fluorescence properties of EEM showed that the fulvic-like components (peak C, peak A and peak M) were dominated in groundwater and river waters, but protein-like components (peak T) was in lake waters. The peak C was observed at $ {{\text{Ex}}} \mathord{\left/ {\vphantom {{{\text{Ex}}} {{\text{Em}}}}} \right. \kern-0em} {{\text{Em}}} = {320 \pm 9} \mathord{\left/ {\vphantom {{320 \pm 9} {424 \pm 5}}} \right. \kern-0em} {424 \pm 5}\;{\text{nm}} $ in groundwater, and 340?±?5/432?±?4 nm in river waters, but the lake waters detected the two peaks, 347?±?7/441?±?11 nm (peak C) as a minor peak and 304?±?2/421?±?8 nm (peak M) as a major peak. Emission wavelength of peak T was observed to shorten in wavelengths from groundwater to river and then lake waters. Peak T in lake waters showed at shorter in wavelengths (279?±?2/338?±?11 nm) at the middle point of Lake Biwa compared to those of lake shore site (283?±?3/350?±?7 nm). Photo-irradiation experiment on upstream waters suggested the changes in the fluorescence peaks of fulvic acid-like substances in lake waters, which might be caused by photo-degradation. DOC concentration was significantly correlated with inorganic anions and EC in river waters. However, such correlations were not observed in groundwater. Anion concentrations in lake waters were low with respect to DOC concentration. These results showed that the optical and chemical properties of FDOM are characteristically varied among groundwater, river and lake waters, indicating the impacts of environments to various FDOM at the same watershed level.  相似文献   

16.
汤婕  张银龙 《土壤》2014,46(4):599-606
全氟辛酸(PFOA)和全氟辛烷磺酸(PFOS)在土壤/沉积物–水中分配、吸附–解吸作用是影响其在环境中的残留浓度、迁移、转化及生物可利用性、毒性等的重要因素之一。本文对土壤/沉积物中PFOA、PFOS吸附–解吸行为影响因素,吸附–解吸机理,常用的土壤/沉积物中PFOA、PFOS吸附/解吸等温线方程、常数及参数等的研究情况进行综述,吸附–解吸过程Freundlich方程的相关系数为0.74~0.99,线性方程的相关系数为0.91~0.99。PFOS在土壤/沉积物中吸附常数logKoc的平均值为3.0,变异系数为23.3%;解吸常数logKoc的平均值为1.8,变异系数为15.4%。PFOA在土壤/沉积物中吸附常数logKoc的平均值为2.1,变异系数为45.6%;解吸常数logKoc的平均值为5.4,变异系数为52.3%。实验室基础上计算所得吸附常数logKoc比野外条件下实测数据计算值(PFOA为3.7,PFOS为4.2)小,野外条件下土壤/沉积物中PFOA和PFOS吸附–解吸过程和土壤–植物共生系统对其污染控制效应有待于进一步研究。  相似文献   

17.
The effect of waterborne zinc on survival, growth, and feed intake of Indian major carp, Cirrhinus mrigala (Hamilton), advanced fry was studied under laboratory condition. Survival rates of C. mrigala advanced fry (2.71?±?0.49 g) after 30 days exposure to control (0.01), 0.03, 0.06, 0.10, and 0.15 mg/L zinc using the static renewal method in freshwater at pH 7.3?±?0.2, temperature 26?±?2°C, and total hardness 114?±?16 mg/L as CaCO3 were 100%. Growth of the fish exposed to 0.10 and 0.15 mg/L of zinc was significantly lower (P?<?0.05) than in control (0.01), 0.03, and 0.06 mg/L of zinc after 30 days of exposure. However, there were no significant differences (P?>?0.05) in fish growth between 0.03 and 0.06 mg/L zinc concentrations. Feed intake rates were significantly (P?<?0.05) reduced in the fish exposed to 0.10 mg/L and higher levels of zinc. The zinc accumulation in the whole body of the fish increased with increasing concentrations of the metal.  相似文献   

18.
Cooking decreases observed perfluorinated compound concentrations in fish   总被引：1，自引：0，他引：1  
Dietary intake is a major route of exposure to perfluorinated compounds (PFCs). Although fish and seafood contribute significantly to total dietary exposure to these compounds, there is uncertainty with respect to the effect of cooking on PFC concentrations in these foods. Eighteen fish species purchased from markets in Toronto, Mississauga, and Ottawa, Canada were analyzed for perfluorooctanesulfonamide (PFOSAs)-based fluorochemicals and perfluorinated acids (PFAs) in raw and cooked (baked, boiled, fried) samples. Of 17 analytes, perfluorooctanesulfonic acid (PFOS) was detected most frequently; concentrations ranged from 0.21 to 1.68 ng/g ww in raw and cooked samples. PFOSAs were detected only in scallops at concentrations ranging from 0.20 ng/g ww to 0.76 ng/g ww. Total concentrations of PFAs in samples were 0.21 to 9.20 ng/g ww, respectively, consistent with previous studies. All cooking methods reduced PFA concentrations. Baking appeared to be the most effective cooking method; after baking samples for 15 min at 163 C (325 degrees F), PFAs were not detected in any of the samples. The margin of exposures (MOE) between the toxicological points of reference and the dietary intake of perfluorocarboxylates (PFCAs) and PFOS in fish and seafood muscle tissue were greater than 4 orders of magnitude. This indicates that reducing consumption of fish muscle tissue is not warranted on the basis of PFC exposure concerns at the reported levels of contamination, even for high fish consuming populations.  相似文献   

19.
Mesta (Hibiscus sabdariffa) is an important fibre crop in the north coastal zone of Andhra Pradesh which accounts for 59% of India's total production of mesta. The area under this crop has reduced dramatically in recent years and in order to understand the contribution of weather to this decline, long-term experimental data (14 years) on mesta cv. AMV-4 and regional crop yields were analysed. Crop yields decreased in seasons when rainfall exceeded 900 mm and maximum temperature remained below 32.0°C during 10–16 weeks after sowing (WAS), which coincided with the active vegetative stage. The average yields of the region were high when seasonal rainfall ranged between 600 and 725 mm. Increased fibre yields were observed when increasing seasonal rainfall coincided with maximum temperatures exceeding 33.5°C. Fibre yields from a long-term experiment showed strong positive correlations with maximum temperature during 6–16 WAS (r = 0.79) and with mean diurnal temperature range (8.6–10.7°C) during 11–19 WAS (r = 0.66). Step-wise regression showed that maximum variability in fibre yield was explained by maximum temperature which could be used to develop models to predict yield at least one month in advance with acceptable accuracy. This prediction could then be used as an input for crop planning and market intelligence.  相似文献   

20.
Synthetic musks are used in many consumer products for their pleasant odor and their binding affinity for fabrics. In the early 1990s, polycyclic musks were reported to occur in air, water, sediment, wildlife, and humans from many European countries. Concentrations of polycyclic musks, particularly 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethyl-cyclopenta-[??]-2-benzopyran (HHCB) and 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronapthalene (AHTN), have been reported to increase over time in the environment. In this study, concentrations of musks in water, sediment, fish, and mussel were determined from three locations along the upper Hudson River. HHCB and AHTN were detected in water (n?=?5; 3.95?C25.8 and 5.09?C22.8 ng/L, respectively), sediment (n?=?3; 72.8?C388 and 113?C544 ng/g, dry weight), fish (n?=?30; <1?C125 and <1?C32.8 ng/g, lipid weight), and zebra mussel (n?=?4; 10.3?C19.3 and 42.2?C65.9 ng/g, lipid weight) samples. Bioaccumulation factors of HHCB calculated for white perch, catfish, smallmouth bass, and largemouth bass were in the range of 18 to 371, when the concentrations in fish were expressed on a wet weight basis; the factors were in the range of 261 to 12,900, when the concentrations in fish were expressed on a lipid weight basis.  相似文献   

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