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1.
巢湖表层沉积物中多环芳烃分布特征及来源 总被引：6，自引：2，他引：4
于2010年,采用野外采样调查、色谱分析与统计比较的方法,研究巢湖表层沉积物中27个采样点中多环芳烃(PAHs)分布特征及污染来源.结果表明:巢湖表层沉积物中检测出的14种优控PAHs总浓度为116.0~2832.2 ng/g(DW),平均值为898.9±791.0 ng/g(DW).多环芳烃组成主要以5~6环PAHs为主,占总量的32%~58%.沉积物中总有机碳含量与PAHs总量呈现良好相关性.利用蒽/(蒽+菲)与苯并[a]蒽/(苯并[a]蒽+屈)比值法对PAHs来源进行解析得出,巢湖表层沉积物中PAHs主要来源为燃烧源.与国内其它水体PAHs含量对比表明,巢湖沉积物中PAHs污染处于中等水平.生态风险评估得出南淝河表层沉积物中PAHs存在生态风险,其它采样点表层沉积物中PAHs生态风险均较低. 相似文献
2.
三峡库区水体和底泥中多环芳烃和邻苯二甲酸酯类分布和来源 总被引：1，自引：0，他引：1
通过对2016年三峡库区干支流18个采样点水体和底泥中16种多环芳烃(PAHs)和6种邻苯二甲酸酯类(PAEs)污染物浓度的时空分布特征和来源进行分析,得出如下结论:三峡库区2016年水体和底泥中ΣPAHs分别为3.9~107.6 ng/L(均值为39.9 ng/L)和267.9~1018.1 ng/g(均值为490.9 ng/g),ΣPAEs分别为122.4~2884.7 ng/L(均值为848.1 ng/L)和192.9~3473.4 ng/g(均值为1253.35 ng/g).水库水体和底泥中PAHs和PAEs均表现出显著的时空分布特征.干支流水体ΣPAHs平均浓度均为放水期(6月)高于蓄水期(12月),干流底泥ΣPAHs平均含量在蓄水期高于放水期.干流水体中ΣPAEs平均浓度在蓄水期显著高于放水期,底泥中ΣPAEs平均含量为放水期高于蓄水期.库区水体中的PAHs以2~3环和4环为主,底泥中以4环和5~6环为主.水体和底泥中PAEs均以邻苯二甲酸(2-乙基已基)酯和邻苯二甲酸二正丁酯为主.库区水体中PAHs的主要来源为焦化或煤焦油挥发、石油源及燃料的中低温燃烧;底泥中PAHs主要来源为煤和生物质燃烧以及石油.水体和底泥中的PAEs主要来源于塑料和重化工工业以及生活垃圾. 相似文献
3.
为明确长江中游地区湖泊沉积物中多环芳烃（PAHs）的分布特征、来源及其生态风险，于2018年7月采集了该地区12个湖泊的表层沉积物样品.采用气相色谱-质谱联用仪（GC-MS）测定了沉积物中16种PAHs的含量.结果表明：12个湖泊沉积物中均检测出16种优控PAHs，PAHs的总含量在572.7~1766.2 ng/g （dw）之间（均值为976.5±285.0 ng/g （dw））.武汉市东湖沉积物中PAHs含量最高，达到1634.8±111.4 ng/g （dw）.与国内外其他地区湖泊沉积物相比，长江中游地区湖泊沉积物中PAHs含量高于国内偏远地区的抚仙湖、青海湖及博斯腾湖，低于东部地区的巢湖、太湖及美国经济工业发达地区的湖泊.根据单体PAH的聚类分析结果，12个湖泊可以分成3种类型，类型1主要以低环为主，占比为64.04%±7.02%，类型2低环和中高环分布相对平均，分别为50.76%±5.17%和49.24%±5.17%，类型3低、中、高环分布相对平均，占比分别为35.35%±3.56%、26.17%±0.45%和38.48%±3.84%.综合该区域PAHs的分布特征及异构体比值法与主成分分析法的结果表明，类型1湖泊沉积物中PAHs主要来源为煤炭、木材等生物质的燃烧源；类型2和类型3湖泊沉积物中PAHs主要来源为煤炭、木材等生物质的低温燃烧以及机动车等燃烧汽油、柴油的尾气排放和工业炼焦等化石燃料的高温燃烧源.沉积物中PAHs与总有机碳（TOC）之间显著的相关性表明，沉积物中TOC含量是影响长江中游湖泊沉积物中PAHs归趋分布的主要因素.长江中游流域湖泊沉积物中PAHs的RQNCs值均小于800，且RQMPCs值大于1的风险商值法生态风险评价结果表明，长江中游流域湖泊表层沉积物中PAHs整体呈中等风险水平. 相似文献
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5.
河北王快水库沉积物多环芳烃的分布、来源及生态风险评价 总被引：6，自引：2，他引：4
对王快水库沉积物中16种多环芳烃含量进行了检测,结果表明,王快水库沉积物多环芳烃含量处于中等污染水平.多环芳烃总含量由库区上游到坝前逐渐升高,多环芳烃总含量在沉积物纵向上的总体分布趋势是随着剖面深度的增加而降低,低环的萘和菲,高环的荧蒽、苯并[b]荧蒽、屈和芘是沉积物中主要的优势化合物,表层和剖面沉积物中多环芳烃的含量与有机碳含量呈正相关关系,相关系数分别为0.8154和0.9534.王快水库沉积物中多环芳烃主要来源化石燃料及生物质的燃烧,风险评价结果表明,严重的多环芳烃生态风险在王快水库沉积物中不存在,但是芴化合物含量超过了风险评价低值,可能存在着对生物的潜在危害. 相似文献
6.
2006年4月在武汉月湖采集了8个样点的水样和表层沉积物样品,采用气-质联用技术分析了样品中25种半挥发性有机污染物(SVOCs)的含量,探讨月湖受有机物污染的程度.水样中25种半挥发性有机污染物总浓度为564.04-1209.41ng/L,平均值为965.64ng/L.沉积物中总浓度为8500.26-23347.20ng/g(DW),平均值为14832.04ng/g(DW).邻苯二甲酸酯类物质是月湖的主要污染物,其中,邻苯二甲酸乙基己基酯和邻苯二甲酸二丁酯含量最高.多环芳烃、硝基甲苯、异佛尔酮等均有不同程度检出,靠近以前的排污口的样点浓度最高.沉积物中25种半挥发性有机污染物的含量大约是水体中含量的15倍,具有潜在生态风险. 相似文献
7.
鄱阳湖周溪湾沉积物中有机氯农药和多环芳烃的垂直分布特征 总被引：3，自引：2，他引：1
通过分析鄱阳湖周溪湾柱状沉积物中有机氯农药(OCPs)和多环芳烃(PAHs)的垂直分布特征,初步探讨该区OCPs和PAHs的污染历史.结果表明,周溪湾柱状样中OCPs总含量范围在40.4~174.1 ng/g(dw)之间,六六六(HCHs)是其主要影响的化合物(16.5~153.6 ng/g(dw)),其次为氯丹类(Chlordanes)和滴滴涕类(DDTs),含量分别为3.4~44.0和1.0~33.4 ng/g(dw).垂直分布特征显示:沉积相上OCPs的残留量比实际使用情况向后推迟10~20年,1950s 1990s OCPs曾被大量使用,到2000年左右在沉积物残留上达到顶峰,随后残留量逐渐降低;而近20年来,该区已经鲜有新的HCHs、Chlordanes以及DDTs输入.PAHs总含量范围为41.3~384 ng/g(dw),芘和菲的含量最高,分别为17.1~67.1和2.68~139 ng/g(dw).垂直分布特征显示,1972年以前,PAHs总含量变幅不大,然而近10年来PAHs的排放量急剧上升.此外,自20世纪末开始,周溪湾区域PAHs的主要来源由以前的煤燃烧释放转化为交通污染排放,并伴随有石油泄漏情况. 相似文献
8.
多环芳烃在小白洋淀挺水植物中的分布、组成及其影响因素 总被引：3，自引：0，他引：3
利用GC-MS测定了端村小白洋淀5个采样点三种主要挺水植物(荷花、蒲草和芦苇)中16种优控多环芳烃(PAHs)的含量,分析了其分布与组成特征及其影响因素。结果表明:(1)16种优控多环芳烃总量(PAH_(16))在三种挺水植物中的平均干重含量范围为82.5-448.6ng/g(dw),七种挺水植物组织荷叶、荷茎、蒲叶、蒲茎、蒲根、苇叶与苇根中PAH_(16)的平均干重含量分别为448.6ng/g(dw)、129.3ng/g(dw)、292.6ng/g(dw)、166.8ng/g(dw)、82.5ng/g(dw)、141.5ng/g(dw)和90.0ng/g(dw),这些数据表明同种植物的叶中PAHs含量最高、茎中次之、根中最低;PAHs各组份在七种挺水植物中的含量具有显著的正相关关系,反映了PAHs在植物组织中的分布模式极为相似.(2)七种挺水植物组织中,均以低环PAHs为主,中环PAHs次之,高环PAHs很低,其百分比范围分别为66.2%(荷叶)-89%(蒲茎)、10.2%(蒲茎)-32.6%(荷叶)和0.6%(蒲叶)-3.7%(苇根);菲、荧蒽、萘、芴、芘和屈6种PAHs组分在挺水植物组织中的平均百分含量较高,分别为35.3%、15.5%、12.1%、11.7%、9.2%和5.2%,占PAH_(16)的89%.3)PAHs在挺水植物中的含量与植物含脂率具有显著的正相关关系,与PAHs组分的辛醇-水分配系数(K_(ow))以及辛醇-大气分配系数(K_(oa))具有显著的负相关关系. 相似文献
9.
为研究乌兹别克斯坦境内阿姆河地区水体中多环芳烃（PAHs）污染特征、来源并进行风险评估,采用高效液相色谱二极管阵列检测器串联荧光检测器法,对研究区域50个采样点中16种优先控制的多环芳烃进行了检测分析.结果表明,阿姆河地区水体中多环芳烃总浓度范围为3.19~779 ng/L,平均值为98.4 ng/L,中位值为40.1 ng/L,单体浓度范围为0~333 ng/L,检出浓度最高的单体为苊烯,5种单体芴、蒽、荧蒽、芘和的检出率为100%,单体苯并[b]荧蒽的检出总量最高,水样中总浓度为786 ng/L,平均值为15.7 ng/L,中值为2.79 ng/L.不同水体含中低环多环芳烃（2~4环）与高环多环芳烃（5~6环）总浓度相近,但不同采样点间浓度差异较大.浓度较高的采样点主要集中在阿姆河三角洲的城市、农业灌溉区及近咸海区域.与世界不同研究区域相比,阿姆河流域多环芳烃浓度处于中等水平.采用相对丰度法、同分异构体比值法及正定矩阵分解法相结合进行源解析,表明研究区域水体中多环芳烃多为混合来源,其中阿姆河下游河段水体多环芳烃主要来源于生物质燃烧,而阿姆河三角洲区域主要来源于生物质燃烧、石油、天燃气燃烧及汽车尾气排放.生态风险评估结果显示,研究区水体单体多环芳烃中萘、苊、菲和蒽的生态风险较低,其余单体处于中等风险等级,其中苯并[b]荧蒽的污染程度较为严重;总体上阿姆河流域ΣPAHs风险等级相对较低,但仍有12和8个点位分别处于中等风险2和高风险等级,且主要集中在阿姆河三角洲地区,需采取相应措施加以控制. 相似文献
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氮是影响和控制水体富营养化的重要因素,不同形态的氮对水体富营养化贡献不同.使用连续提取法对东苕溪干流悬浮物、表层沉积物样品中各形态氮含量进行测定,探讨各形态氮的分布特征及其影响因素.结果表明,东苕溪水体氮污染严重,总氮浓度均值为4.48 mg/L.悬浮物中各形态氮含量均高于沉积物,其中悬浮物中铁锰氧化态氮(IMOF-N)含量所占比例最大,均值为1506.94 mg/kg;沉积物中有机硫化物结合态氮(OSF-N)含量最高,均值为625.31 mg/kg.IMOFN、OSF-N含量受阳离子交换量、粒径影响显著,均与总氮浓度显著相关.相关性分析表明水体的性质对IMOF-N及OSF-N含量影响较显著,并且总体上对悬浮物的影响强于沉积物.另外,悬浮物有助于水体中的氮发生硝化反应向硝态氮转化,沉积物则有助于水体的氮发生还原作用向氨氮转化.在一定程度上,水体中的悬浮物对藻类具有抑制作用. 相似文献
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The polycyclic aromatic hydrocarbons (PAHs) pollution in the Sarno River and its environmental impact on the Gulf of Naples (Tyrrhenian Sea, Central Mediterranean Sea) were estimated. The 16 PAHs identified by the USEPA as priority pollutants and perylene were determined in the water dissolved phase (DP), suspended particulate matter (SPM) and sediments. Total PAHs concentrations ranged from 23.1 to 2670.4 ng L(-1) in water (sum of DP and SPM) and from 5.3 to 678.6 ng g(-1) in sediment samples. Source analysis revealed that PAHs mainly came from combustion process. Contaminant discharges of PAHs into the sea were calculated in about 8530 gd(-1) showing that this river should account as one of the main contribution sources of PAHs to the Tyrrhenian Sea. 相似文献
12.
Distribution and sources of polycyclic aromatic hydrocarbons (PAHs) in sediments from Zhanjiang Bay and Leizhou Bay, South China 总被引：4，自引：0，他引：4
The concentrations and spatial distribution of polycyclic aromatic hydrocarbons have been investigated in two adjacent bays of Zhanjiang and Leizhou, China. The total concentrations of the 16 USEPA priority PAHs were ranged from 41.96 to 933.90ng/g dry weight with an average concentration of 315.98ng/g and ranged from 21.72 to 319.61ng/g with an average concentration of 103.91ng/g in Zhanjiang and Leizhou Bays, respectively. The spatial distribution of PAHs was site-specific and appeared to be somewhat positively correlated with TOC and negatively correlated with sediment grain size in the two bays. The values of Phe/Ant, BaA/228 and InP/276 were higher than 10, less than 0.2, and from 0.2 to 0.5, respectively, indicating that the sources of PAHs in the two bays were mainly from petroleum and its combustion, which predominantly originated from those ships and boats coming and going in the two bays. 相似文献
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Occurrence of polycyclic aromatic hydrocarbons (PAHs) in seawater from the Western Taiwan Strait, China 总被引：6，自引：0，他引：6
Seawater samples (including surface water and bottom water) were collected from the Western Taiwan Strait (WTS) during June 24-25, 2009; polycyclic aromatic hydrocarbons (PAHs) in dissolved phase and particulate phase were analyzed, respectively. The results showed that the total concentrations of PAHs in the dissolved phase and particulate phase were ranged from 12.3 to 58.0 ng L(-1), and 10.3-45.5 ng L(-1), which showed a low-middle contamination level in the China Seas. The spatial variability of PAHs may be related to the complicated currents of WTS, especially the Min-Zhe coastal current. PAHs diagnostic ratios suggested that PAHs mainly originated from the inputs of pyrolytic (combustion) sources, which might be contributed to land-based atmospheric deposition. The particle-water partition coefficients of individual PAH showed that partitions were not correlated with suspended particulate matter content, dissolved organic carbon or salinity, similar to the Yangtze coastal area. 相似文献
14.
Humin Zong Xindong MaGuangshui Na Chuanlin HuoXiutang Yuan Zhifeng Zhang 《Marine pollution bulletin》2014
Polycyclic aromatic hydrocarbons (PAHs) were detected in water and sediment samples collected from three mariculture zones in China’s northern Yellow Sea. In these samples, total PAH concentrations ranged from 110.8 ng/L to 997.2 ng/L and 142.2 ng/g dry weight (dw) to 750.2 ng/g dw, respectively. The log KOC values of the various PAH compounds examined in this study increased with the log KOW values, which is consistent with the prediction regarding PAH behavior in the environment. However, these KOC values were lower than the predicted values as a result of the effects of organic matters, which were abundant in the mariculture water. The isomeric ratios of the PAHs in sediment indicated that the source of the PAHs in the mariculture zones were mainly pyrolytic. The TEQcarc values of PAHs ranged from 7 ng TEQ/g dw to 92 ng TEQ/g dw, and only a few samples met the safe criterion with respect to individual PAH concentrations. 相似文献
15.
The distribution of polycyclic aromatic hydrocarbons (PAHs) between various phases is fundamental in the control of their movement and impact in the marine environment. In this study samples of water and sediments were regularly collected from Brighton marina, UK, to quantify the intensity, spatial and temporal variations of PAH contamination. The results show clearly that PAH behaviour in marine systems is highly complex, and controlled by the interplay of PAH sources, compound physicochemical properties, water and sediment movement, and field conditions. Levels of total PAHs (16 compounds) in the dissolved phase were found to vary between <2 and 11,400 ng/l, with higher values observed in the winter months. Total PAH concentration in sediment samples varied between 24 and 4710 ng/g dry weight. PAHs in water were dominated by low molecular mass compounds (2-ring), while PAHs in sediments were mainly derived from 2-4 ring compounds. In addition, dissolved concentrations were increased during sediment dredging and after a period of severe rainfall. PAHs in Brighton marina are likely to be from both pyrolytic and petrogenic sources; as a result, field-derived distribution coefficients for individual PAHs between sediment and water tend to follow the equilibrium partition models, although slight exceedance is apparent. The extended partition model incorporating soot carbon has achieved limited success in better predicting PAH behaviour. 相似文献
16.
Polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs) were measured in suspended particles and dissolved phase from the Baiertang water column and the Macao water column samples as collected from the Guangzhou channel of the Pearl River and the Macao harbor, where the sediments were heavily contaminated with organic pollutants. Total OCPs concentration varies from 23.4 to 61.7 ng/l in Baiertang water column and from 25.2 to 67.8 ng/l in Macao column, while total PAHs concentration varies from 987.1 to 2878.5 ng/l in the Baiertang water column and from 944.0 to 6654.6 ng/l in the Macao column. The vertical distribution profiles of pollutants and the partition of pollutants between particles and dissolved phases indicate that the sediments in Baiertang act as an important source of selected pollutants, and the pollutants in water of this region were mainly originated from the release and re-suspension of contaminants residing in the sediments. The sediments in Macao harbor act as a reservoir for organochlorine pesticides, such as DDTs mainly introduced by river inflow from Xijiang and PAHs input by brackish water from the Lingdingyang estuary. Combustion of fossil fuels and petroleum input are the main sources of PAHs in the Macao water column, while combustion of fossil fuels and coal is responsible for the PAHs in the Baiertang water column. The ratios of DDT/(DDD+DDE) for the Macao water column samples demonstrate that such chemicals were input into this region in recent times. 相似文献
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《Marine pollution bulletin》2014,81(1-2):52-58
The contamination of surface sediments in Guan River Estuary, China, by polycyclic aromatic hydrocarbons (PAHs) has been fully investigated. Total concentrations of 21 PAHs ranged from 90 to 218 ng/g with an average of 132.7 ng/g, which is relatively low in comparison with other estuaries around the world. PAH concentrations appeared to be positively correlated with clay content and negatively correlated with sediment grain size. Source identification implied that the PAHs originated mainly from pyrolytic sources. However, source patterns may be continuously changed to a petrogenic origin due to the heavy ship traffic and continuous discharge of oily sewage in this area. The PAH levels were also compared with international Sediments Quality Guidelines and Sediments Quality Criteria, and the results indicated low negative effects for most individual PAHs. However, toxic effects related to FLO would occur occasionally in most locations in the estuary. 相似文献