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1.
钦州湾河流沉积物中镭的解吸行为 总被引：1，自引：0，他引：1
放射性镭同位素在海底地下水排放（SGD）等海洋物质变化过程的研究中具有优良的示踪作用，估算SGD通量时需要计算河流悬浮颗粒物的解吸通量。因此，对河流沉积物/悬浮颗粒物中镭同位素解吸行为的研究不可或缺，而目前对于粒度较小范围内镭同位素的解吸特征及其机理的研究依然不足。本文选用钦州湾河流沉积物，通过室内实验探究粒度和盐度对沉积物中镭同位素解吸行为的影响。结果表明，在沉积物平均粒径0.9~136.0 μm范围内，随着粒径增大，沉积物中镭同位素在海水（盐度为33.9）中解吸活度逐渐减小，且变化趋势也逐渐变缓，平均粒径大于43.7 μm后，解吸量几乎不变；在海水盐度4.9~33.9范围内，随着盐度增大，沉积物中镭同位素解吸活度逐渐增大，盐度大于24.9后，解吸量趋于不变。本文创新性地建立了沉积物表面分形结构的镭解吸理论模型，拟合得到钦州湾河流沉积物表面最大可交换态224Ra、226Ra和228Ra活度分别为1.13 dpm/g、0.17 dpm/g和0.85 dpm/g，以干重计；沉积物中224Ra、226Ra和228Ra最大解吸比分别为30%、7%和18%。钦州湾河流沉积物颗粒表面最大可交换态224Ra和226Ra活度分别处于全球中等水平和较低水平，而其最大解吸比分别处于全球较高水平和较低水平。本研究结果有助于更好地理解镭同位素的解吸行为，以帮助更准确地估算SGD通量。 相似文献
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吸附材料再生可以实现吸附材料的循环使用,降低处理成本。本文研究了壳聚糖-生物炭复合材料上诺氟沙星(NOR)解吸的影响因素,考察了NOR解吸动力学过程,并通过多次再生实验探讨了其重复使用潜力。结果表明,以NaOH为解吸剂时有利于促进壳聚糖-生物炭复合材料上NOR的解吸,随NaOH浓度的提高,NOR的解吸率增大。溶液离子强度提高了NOR的解吸率,离子强度为0.1mol/L时NOR的解吸效果最好。热力学参数ΔG和ΔS表明该解吸过程是自发进行的吸热反应。NOR在壳聚糖-生物炭复合材料上的解吸主要受慢解吸和极慢解吸控制。双常数方程和Elovich方程可较好描述复合材料上NOR的解吸动力学行为。壳聚糖-生物炭复合材料重复使用6次后,NOR的解吸率为66.88%,吸附量为8.675mg/g,表明壳聚糖-生物炭复合材料具有较好的可循环利用潜能。 相似文献
3.
黄河三角洲北部湿地多环芳烃分布与来源 总被引：4，自引：0，他引：4
对黄河三角洲北部湿地表层土壤中的多环芳烃（PAHs）进行定量分析，结果表明，袁层土壤中PAHs总量范围为27．43～128．97ng／g（干重），PAHs的空间分布总体呈西高东低的趋势。经过研究对比，认为表层土壤样品中的PAHs尚未对生物造成显著负面影响，并提出表层土壤PAHs污染主要来源于高温热解产物，仅有很小部分的石油类的污染。 相似文献
4.
盐度对镭同位素在海南红树林沉积物解吸行为的影响 总被引：1，自引：0，他引：1
天然放射性镭同位素在沉积物上的解吸行为是影响其在陆-海交换过程中的关键所在。采用沉积物室内解吸实验和现场采集间隙水测量224Ra含量两种方法,对水体盐度梯度控制镭在海南八门湾红树林沉积物的解吸行为进行了讨论。结果表明:沉积物上可交换态224Ra的最大量为0.44dpm/g,解吸比为35%。利用间隙水的224Ra含量确定镭的分配比Kd与水体盐度S呈反比例函数:Kd=8.4×102/S,与室内解吸实验的结果相比更能代表镭在沉积物上的真实解吸行为。在深度25—40cm内,湿地沉积物的224Ra处于与其母体228Th的平衡状态,但223Ra很可能处于相对其母体227Th亏损状态。 相似文献
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6.
2007年11-12月采集福建和粤东近岸海域的沉积物样品,对沉积物中的PAHs含量、组成进行研究,分析了研究海域沉积环境中PAHs的分布特征、来源,并利用Long等人建立的评价模式对PAHs的生态风险进行了评价.研究结果为深入研究海域沉积环境中PAHs的地球化学行为提供了科学依据.结果表明：研究海域PAHs的含量范围为52.93-398.50 ng/g,平均值为170.30 ng/g,研究发现闽江径流是影响海区沉积物中PAHs含量分布的重要因素之一.通过不同环数PAHs的相对丰度和异构体比值分析,对研究海区沉积物中PAHs进行了溯源分析,发现厦门以北海域沉积物中的PAHs主要来自化石燃料燃烧,而厦门以南海域则主要来源于石油污染.生态风险评价结果显示,研究海域PAHs对生物体极少产生负面生态效应,潜在生态风险很小. 相似文献
7.
厦门西海域表层水中PAHs污染与PAHs降解菌分布的关系 总被引：12，自引：0，他引：12
在厦门西海域设置6个站位，于2001年7月和10月两个航次对各站位表层水中多环芳烃(polycyclic aromatic hydrocarbons，PAHs)的含量及几种常见PAHs的降解菌的数量进行调查，结果表明：表层水中PAHs的含量很不稳定，存在明显的时间变化。在7月的调查中，表层水中能检测到的PAHs以2—3环的为主，而在10月以46环的为主。低分子量的PAHs——芴和菲的含量与其降解菌的数量之间具有明显的正相关，而高分子量的PAHs—荧蒽和芘的含量与其降解菌的数量之间没有表现出相关性。 相似文献
8.
中国北部辽东湾表层沉积物中PAHs源解析和生态风险评价 总被引：1，自引：0，他引：1
ZHANG Yufeng WU Jinhao SONG Lun SONG Yonggang YANG Meng WANG Nianbin HAN Jiabo GUAN Daoming 《海洋学报(英文版)》2018,37(4):12-21
研究于2014年和2015年对辽东湾表层沉积物中16种多环芳烃（PAHs）的来源和生态风险状况进行了调查和评估。辽东湾表层沉积物中16种PAHs的含量范围为88.5-347 ng/g，高值区主要分布在辽东湾中部海域。对辽东湾各站位沉积物中多环芳烃的含量进行中聚类分析结果表明，辽东湾的采样站位可分为两类，一类站位主要分布在辽东湾沉积物中部海域，另一类站位主要分布在受陆源污染较为严重的近岸海域。辽东湾表层沉积物中PAHs的来源为燃烧源和石油源的混合来源，其中燃烧源为主要来源。萘、苊、苊烯、菲、二苯并[a,h]蒽可能偶尔会引发有害生物效应；辽东湾表层沉积物为低致癌风险；辽东湾中部海域表层沉积物中PAHs的生态风险和毒性污染水平高于辽东湾近岸海域。 相似文献
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大亚湾海域多环芳烃和有机氯农药的高分辨率沉积记录 总被引：6，自引：0，他引：6
以GC／ECD和GC／MS内标法分析测定了大亚湾沉积物柱样（DYW03—8）中多环芳烃（PAHs）和有机氯农药（0CPs）的含量，结合^210Pb定年，重建了该海域近50年来PAHs和OCPs的污染历史，并对其可能的来源和输入途径进行了探讨。结果表明，近50年来该海域沉积物中PAHs和OCPs的含量总体上均呈上升趋势，且一般都在上世纪90年代以后这种上升变得更加明显；PAHs主要来源于化石燃料的不完全燃烧，即热成因，并可能主要通过大气颗粒物沉降以及工业和生活污水的直接排放等途径进入水体沉积物中；HCHs和DDTs的组成特征及其变化趋势揭示，该区可能曾大量使用过林丹（γ-HCHs）作为杀虫剂，近15年来随着该地区各种经济开发活动的加强，残留在土壤中的这些农药组分更多地随地表径流进入到水体沉积物中。同时，DDTs类农药也可能仍存在新的输入源，但这种输入的强度在近几年似乎有所减弱。 相似文献
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分析了海运船舶尾气洗涤废水排放对多环芳烃 (PAHs) 类污染物的海洋富集行为的影响以及对 PAHs 控制的制约因 素和净化技术发展现状。PAHs 的海洋富集趋势与船舶的发动机尾气排放行为呈正相关性, 且船舶尾气洗涤废水排放加速了 PAHs 向海洋中富集。 国际海事组织 (IM0) 尚未对在PAHs 中占比大且毒性强的烷基化多环芳烃进行立法限制, 但单方面采 取措施禁止船舶尾气洗涤废水在其所属海域排放的国家和地区日益增多, 洗涤废水排放的PAHs 类污染物亟须净化处理。将 高级氧化光催化技术应用于洗涤废水排放的PAHs 净化具有发展前景。我国应抓住机遇, 大力开展针对海洋 PAHs 的排放限 制立法以及船舶尾气洗涤废水处理先进技术的研究, 这对于提升我国海事管理水平、增大国际话语权, 以及保护海洋生态安 全具有重要意义。 相似文献
11.
夏季珠江口水体中多环芳烃的分布、组成及来源 总被引：2，自引：0，他引：2
利用1999年7月对珠江口海域的调查资料,对该区表层海水中优控多环芳烃的分布、组成及来源进行了分析和讨论,结果表明:(1)夏季珠江口海域表层海水中14种溶解态多环芳烃[苊、芴、菲、蒽、荧蒽、芘、苯并(a)蒽、艹屈、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、二苯并(a,h)蒽、苯并(g,h,i)艹北、茚并(1,2,3-cd)艹比]的质量浓度为63.8~171.7 ng/L,且沿着冲淡水流向呈降低趋势;(2)颗粒态中15种多环芳烃[萘、苊、芴、菲、蒽、荧蒽、芘、苯并(a)蒽、艹屈、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、二苯并(a,h)蒽、苯并(g,h,i)艹北、茚并(1,2,3-cd)艹比]的质量浓度为60.7~186.7 ng/L,其分布与水体载沙量及悬浮颗粒物的性质、粒径有关,具有从河口内向外海降低的分布特征;(3)多环芳烃组成和特征参数比值的分析表明,珠江口海域高温裂解来源的多环芳烃在伶仃洋海区输入最多,且主要为人类活动中煤燃烧排放的,而在香港岛周围海区的输入则相对较少,且主要为油燃烧排放的;(4)与法国塞纳河及长江口等河口相比,珠江三角洲海域水体中存在高菲含量排放源。 相似文献
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Stress proteins (heat shock proteins, hsps) form part of the cellular protein repair system, and are induced by a wide variety of Stressors. To determine their suitability as tools for assessing sublethal sediment toxicity, we measured levels of members of the stress protein families hsp60 and hsp70 in benthic estuarine amphipods (Ampelisca abdita) exposed to sediments from 23 different sampling sites in San Francisco Bay for 10 d. Concentrations of sediment-associated xenobiotics were determined. Per cent survival was recorded and surviving animals were analysed for stress proteins using western blotting techniques. An inverse correlation (r2 = 0.44) was seen between amphipod survival and hsp64 levels, and hsp64 levels were positively correlated with concentrations of total polycyclic aromatic hydrocarbons (PAHs) (r2 = 0.5). Principal component analysis revealed that amphipod mortality was linked to a combination of several PAHs (phenanthrene, fluoranthene, pyrene, benzo(a)pyrene) and di-n-butylphthalate at southern San Francisco Bay sites. At northern San Francisco Bay sites, negative correlations were found between hsp64 levels and organotin compounds (MBT, DBT, TBT), and between hsp71 levels and the PAHs, benzo (b,k)fluoranthene and benzo(G,H,I)perylene, suggesting an inhibitory effect of these compounds on stress protein expression. 相似文献
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Polycyclic aromatic hydrocarbon (PAH) bioaccumulation by the polychaete worm Streblospio benedicti (Webster) was measured under exposure to PAH-contaminated sediments in the field and for 28 d in the laboratory. Streblospio benedicti collected from field sediments contaminated at 2.94, 1.07, and l.52 μg g−1 fluoranthene (FLU), benz[a]anthracene (BAA), and benzo[a]pyrene (BAP), bioaccumulated those PAHs at 1.53, 0.215, and 0.332 μg g−1, while worms isolated from less contaminated field sediments (0.399, 0.228, 0.288 μg g−1 FLU, BAA, and BAP) had FLU, BAA, and BAP body burdens of 0.543, 0.236, and 0.083 μg g−1. Worms incubated for 28 d in PAH-spiked sediments (1.52, 0.991, 0.504 μg g−1 FLU, BAA, and BAP) bioaccumulated those PAHs at 0.382, 0.966, and 0.602 μg g−1, respectively. Data normalization to organism lipid and sediment organic carbon (biota-sediment accumulation factors [BSAFs] strongly suggest that Streblospio PAH bioaccumulation was directly related to percent sediment organic carbon, but BSAFs were substantially lower than predicted by equilibrium partitioning theory. BSAFs decreased with increasing PAH log Kow, in worms collected from field sediments, but in spiked sediments BSAFs increased with increasing PAH hydrophobicity. This disparity may have been caused by insufficient spiked-sediment equilibration time (1.5h) in the case of the laboratory test sediments. 相似文献
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In order to understand the diversity and distribution of the bacterial community in the coastal sediment of the Bohai Bay,China,high-throughput barcoded pyrosequencing of the 16 S r RNA gene was used.Metagenomic DNA was extracted from the sediment samples,and was sequenced using a 454 GS FLX Titanium system.At 97%similarity,the sequences were assigned to 22 884 operational taxonomic units(OTUs) which belonged to 41 phyla,84 classes,268 genera and 789 species.At the different taxonomic levels,both the dominants and their distribution varied significantly among the six coastal sediments.Proteobacteria was the first dominant phylum across all the six coastal sediments,representing 57.52%,60.66%,45.10%,60.92%,56.63% and 56.59%,respectively.Bacteroidetes was the second dominant phylum at Stas S1,S2 and S4,while Chloroflexi was the second dominant phylum at Stas S3,S5 and S6.At class level,γ-Proteobacteria was the first dominant class at Stas S1,S2,S4 and S6,while δ-Proteobacteria became the first dominant class at Stas S3 and S5.In addition,a large proportion of unclassified representatives have distributed at the different taxonomic levels.Canonical correspondence analysis(CCA) results indicated that the sediment texture,water depth(D),dissolved oxygen(DO),total nitrogen(TN) and nine EPA priority control polycyclic aromatic hydrocarbons(PAHs) including naphthalene,acenaphthylene,acenaphthene,fluorine,phenanthrene,fluoranthene,pyrene,benzo[a]anthracene and indeno[1,2,3-cd]pyrene were the important factors in regulating the bacterial community composition.Those results are very important to further understand the roles of bacterial community in the coastal biogeochemical cycles. 相似文献
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The scope of this work was to evaluate the levels of polycyclic aromatic hydrocarbons (PAHs) and their possible sources in two shallow sediment cores from an estuarine area located in the south region of Brazil, the Guaratuba Bay. The estuary is encompassed by an Environmental Protection Area (EPA) of 1306 km2, which is still considered to be pristine, despite recent urban growth. To assess levels of 14 selected PAHs in the sediments, among those listed as “priority pollutants” by the US Environmental Protection Agency, the cores were divided in several sections, followed by extraction, clean-up, fractionation and subsequent analysis using HPLC coupled to a fluorescence detector. Among the PAHs detected, phenanthrene and fluoranthene showed the highest concentrations. PAHs with more than four rings were usually present in low concentrations or were undetectable. To assist in the identification of possible sources, the ratios An/(An + Phe) and Flt/(Flt + Py) (anthracene to anthracene plus phenanthrene and fluoranthene to fluoranthene plus pyrene) and a PCA model were also used. Total concentrations of PAHs ranged between 1.5 and 3130 ng/g (mean 495) dry weight for the core collected in the inner part of the estuary, and between 78.5 and 3270 ng/g (mean 899) dry weight for the other core, collected in the outer part. Compared to values found in other studies in coastal zones along South American eastern margin, this area can be considered to range from low polluted to moderately polluted. From the data, it was also possible to conclude that there is predominance of petroleum sources, and essentially close to the more urbanised areas. Combustion sources have only minor contribution and are episodic, when compared to the latter. 相似文献
16.
海洋微生物对多环芳烃的降解 总被引：15，自引：1，他引：15
从海域沉积物中富集分离出以芘作为唯一碳源和能源的海洋微生物，以ST4富集培养的混合微生物作为研究对象；该海洋混合菌株能利用菲（Phe）、芘（Pyr)、荧蒽（Fla)等多种多环芳烃；在不同浓度的芘的降解中，当芘的浓度为50mg/dm^3时，其生长水平和降解速率最高；当芘的浓度为200mg/dm^3时，其生长受到抑制，芘几乎不能被降解。外加营养盐酵母浸出液和葡萄糖促进降解微生物的生长，提高降解速率。研究表明了海洋微生物在多环芳烃污染环境的生物修复应用前景。 相似文献
17.
R.H.M. Eertman C.L.F.M.G. Groenink B. Sandee H. Hummel A.C. Smaal 《Marine environmental research》1995,39(1-4)
The polycyclic aromatic hydrocarbons fluoranthene and benzo(a)pyrene significantly reduced the feeding rate of mussels. For both compounds the tissue concentration resulting in a 50% reduction of the clearance rate (TEC50) was calculated. At high tissue concentrations both aromatic compounds reduced the tolerance of mussels to aerial exposure, whereas at low tissue concentrations an improved response was noticed. The activities of the antioxidant enzymes Superoxide dismutase (SOD) and catalase were elevated only at low tissue concentrations of fluoranthene and benzo(a)pyrene. At the highest measured tissue concentrations the activity of both enzymes was reduced, possibly due to a narcotic effect. The reproductive success rate of mussels appeared to be affected negatively by the investigated hydrocarbons. The results of a pilot experiment indicate that mussels can be used also for the testing of contaminated sediments. 相似文献
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Seven stations were established in the Quanzhou Bay (24.73°-24.96°N, 118.50°-118.70°E) in China on three cruises to determine the concentrations of polycyclic aromatic hydrocarbons (PAHs) and the numbers of PAH-degrading bacteria in surface sediments. Assessing the biodegradation poten- tial of indigenous microorganisms by measuring the respiratory intensity with the addition of PAHs in sediment samples was also one of the aims of this study. The results show that the total PAH concentrations of the sedimen... 相似文献