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371.
Cláudia Ribeiro Ana Rita Ribeiro Maria Elizabeth Tiritan 《Journal of environmental science and health. Part. B》2016,51(3):143-153
Persistent organic pollutants (POPs) are widespread compounds, such as organohalogenated compounds, polycyclic aromatic hydrocarbons (PAHs) and pesticides, which can be found in all types of environmental compartments. Their presence in the aquatic environment is a worldwide problem, with emphasis on sediments which act as depository and consequently as a source of hydrophobic, recalcitrant and harmful compounds. Besides, these pollutants might affect the reproduction and mortality of living organisms, diverging in their potential to bioaccumulate in tissues. The present paper aims to review the occurrence of POPs in sediments and biota from the coastal, estuarine and river areas of Portugal. The list of the studied compounds comprises organohalogenated compounds, PAHs, organometallic compounds, pesticides, sterols, fatty acids and pharmaceutical compounds. The contamination of sediments by various pollutants is presented, such as PAHs up to 7,350 ng g?1 found in Sado estuary and polychlorinated biphenyls up to 62.2 ng g?1 in the case of sediments collected in Ria de Aveiro. The occurrence of these persistent toxic substances in sediments demonstrates aquatic contamination from agricultural, industrial and urban discharges and the concern about the potential risks to aquatic organisms, wildlife and humans. In fact, several classes of POPs have also been found in biota, such as polychlorinated biphenyls up to 810.9 ng g?1 in sentinel fish from the Douro River estuary and pesticides in bivalves from the Sado River estuary. The importance of further systematic research on sediments and biota is here highlighted to compare the contamination of these two reservoirs; to assess their spatial and temporal variation; and to determine other classes of POPs that were not investigated yet (e.g., industrial compounds, estrogens and many classes of pharmaceuticals). 相似文献
372.
D. Golomb E. Barry G. Fisher P. Varanusupakul M. Koleda T. Rooney 《Atmospheric environment (Oxford, England : 1994)》2001,35(36)
Wet and dry deposition of polycyclic aromatic hydrocarbons (PAHs) was measured at Nahant, Massachusetts, a peninsula jutting into Massachusetts Bay and Wolf Neck, a peninsula jutting into Casco Bay, Maine. Wet deposition (rain and snow) was collected in a funnel which drains into a shielded, temperature controlled receiving bottle. Dry deposition of gaseous and particulate PAHs was collected onto an exposed water surface. PAHs were analyzed by solid phase extraction and gas chromatography-mass spectrometry. Sixteen PAH species were analyzed, ranging from acenaphthylene to coronene. The mean wet deposition rate of the sum of the 16 species is 720 ng m−2 cm−1 precipitation at Nahant, and 831 ng m−2 cm−1 precipitation at Wolf Neck. Wet deposition is attributed to regional PAH emitting sources. Storm patterns appear to bring somewhat higher wet deposition of PAHs to Wolf Neck than to Nahant. The mean dry deposition rate is 95 ng m−2 h−1 at Nahant and 9.3 ng m−2 h−1 at Wolf Neck. The large difference is attributed to the fact that Nahant is close to the urban-industrial metropolitan Boston area and Logan International Airport, whereas Wolf Neck has no major PAH-emitting sources nearby. Individual measurements have an error bracket of ±30%. The Chemical Mass Balance model was used to apportion the dry deposition to source categories. At Nahant, nine samples gave valid statistical attributes with a mean apportionment: jet exhaust 35%, gasoline fueled vehicles 32%, diesel fueled vehicles 17%, wood combustion 13%, others 3%. At Wolf Neck, six samples yielded a mean apportionment: jet exhaust 30%, gasoline vehicles 28%, diesel vehicles 18%, wood combustion 16%, others 8%. There is a considerable variation between the samples. The apportionment is greatly dependent on the quality and selection of the model inputs, i.e. source signatures, which for PAHs are questionable. 相似文献
373.
卤代芳烃对水生生物急性毒性的定量构效关系研究 总被引：3，自引：0，他引：3
提出表征成键原子生物活性的点价 βi,由 βi 建构新的价连接性指数nH ,并用 0阶指数0 H ,1价指数1H研究了卤代芳烃 (含F、Cl、Br、OH、NH2 、NO2 和烷基等 )对发光菌、呆鲦鱼、斜生栅列藻的急性毒性 ,给出了相关方程。结果表明 ,新方法计算简单 ,应用方便 ,估算结果均优于相应的文献方法 相似文献
374.
Light nonaqueous-phase liquids (LNAPLs) such as gasoline and diesel fuel are among the most common causes of soil and groundwater contamination. Dissolution and subsequent advective transport of LNAPL components can negatively impact water supplies, while biodegradation is thought to be an important sink for this class of contaminants. We present a laboratory investigation of the effect of a water-table fluctuation on dissolution and biodegradation of a multi-component LNAPL (85% hexadecane, 5% toluene, 5% ethylbenzene, and 5% 2-methylnapthalene on a molar basis) in a pair of similar model aquifers (80 cm x 50 cm x 3 cm), one of which was subjected to a water-table fluctuation. Water-table fluctuation resulted in LNAPL and air entrapment below the water table, an increase in the vertical extent of the LNAPL source zone (by factor 6.7), and an increase in the volume of water passing through the source zone (by factor ~18). Effluent concentrations of dissolved LNAPL components were substantially higher and those of dissolved nitrate lower in the model aquifer where a fluctuation had been induced. Thus, water-table fluctuation led to enhanced biodegradation activity (28.3 mmol of nitrate consumed compared to 16.3 mmol in the model without fluctuation) as well as enhanced dissolution of LNAPL components. Despite the increased biodegradation, fluctuation led to increased elution of dissolved LNAPL components from the system (by factors 10-20). Hence, water-table fluctuations in LNAPL-contaminated aquifers might be expected to result in increased exposure of downgradient receptors to LNAPL components. Accordingly, water-table fluctuations in contaminated aquifers are probably undesirable unless the LNAPL is of minimal solubility or the dissolved-phase plume is not expected to reach a receptor due to distance or the presence of some form of containment. 相似文献
375.
376.
377.
多环芳烃类化合物(PAHs)是环境中普遍存在的持久性有毒有机污染物,因具有强烈的\"三致\"作用,业已引起各国环境科学工作者的广泛关注,PAHs污染土壤的修复也已成为环境科学与工程领域的研究热点。以菲为PAHs的代表,研究了黑麦草/苜蓿间作对多环芳烃(菲)污染土壤的修复效应。通过温室盆栽模拟实验,观察到5 mg/kg和50 mg/kg污染水平没有明显抑制黑麦草和苜蓿的生长;黑麦草/苜蓿间作促进了植物对土壤菲的吸收,且间作体系根系富集系数大于单作;土壤中菲的可提取浓度随时间的延长逐渐减少,在菲重度污染土壤上,黑麦草/苜蓿间作修复效果明显优于单作,菲去除率可高达90.53%。因此,对于重度PAHs污染土壤该体系是一种有实际应用价值的间作修复体系。 相似文献
378.
为研究超声波技术处理石油污染土壤的影响因素,选取了土壤含油量、土水比、土壤类型、超声处理时间和超声功率5个因素进行了具有交互作用的正交实验,并讨论了各因素对土壤中石油污染物清除率的影响。实验结果表明超声波对土壤中石油污染物的净化效果明显,总石油烃(TPH)的清除率在23.0%到77.3%之间,土壤类型对净化效果的影响最为显著,粘土中的TPH清除率显著低于砂土。由超声空化引起的解吸作用和真空抽滤是实验过程中土壤TPH减少的主要途径。研究结果表明超声波技术用于石油污染土壤修复是可行并且有效果的。 相似文献
379.
大体积进样技术结合同位素稀释法测定地表水中多环芳烃的研究 总被引：1，自引：0，他引：1
采用C18固相萃取柱预处理水样,由于固相萃取柱的选择吸附性,净化了样品的基质;同液-液萃取相比,固相萃取柱和硅胶小柱的双重净化,更适合大体积进样。萘、苊、菲、屈艹的氘代化合物作为同位素稀释剂,由于待测分析物与同位素稀释剂物理化学的相似性,其在固相萃取柱的保留行为和色谱运行行为都有基本一致性。同一般内标法相比,同位素稀释法具有较高的回收率。大体积进样由于进样绝对量的增加,降低了检出限。方法检出限0.05～0.1ng/L,回收率范围90%～110%。 相似文献
380.
用竹炭固相萃取恒波长同步荧光法测定了九龙江龙岩段水体中16种优控多环芳烃(PAHs)的含量。结果表明:龙岩市省控断面河水中2010年11月(冬季)多环芳烃的质量浓度为58.3×10-9~1 328.5×10-9g/L,平均为387.72×10-9g/L;2011年9月(秋季)水中总多环芳烃质量浓度为5.9×10-9~188.4×10-9g/L,平均为77.46×10-9g/L;7月(夏季)多环芳烃的质量浓度为16.7×10-9~1 203.3×10-9g/L,平均为475.05×10-9g/L,同国内外河流相比,九龙江龙岩段水体中PAHs污染较严重,且具有明显的季节分布特征。夏、秋、冬季九龙江龙岩段水体水中均以3~4环PAHs为主。污染来源分析表明,河水中PAHs主要来源于燃烧源。 相似文献