大兴安岭摩天岭雨养泥炭沼泽多环芳烃分布特征与来源分析

运用气相色谱—质谱(GC-MS)技术对大兴安岭摩天岭(47°22′23″N,120°38′45″E)雨养泥炭沼泽泥炭柱中的多环芳烃(PAHs)污染物进行了分析。结果表明,研究区雨养泥炭沼泽表层PAHs总含量的质量比为1 874.4 ng/g,与国内外雨养泥炭沼泽表层相比,其污染水平相对较高。由于研究区气候冷湿,雨养泥炭沼泽中的有机质腐殖化程度较低,有机碳含量较高,这和其PAHs含量的相关性较小。研究区样品中检测出的PAHs主要以2~3环的多环芳烃为主;由PAHs分子标志物指标分析结果可知,研究区雨养泥炭沼泽PAHs污染物的主要来源是当地森林火灾与大气远距离沉降;沉降的PAHs污染物是原油开采、石油生产和化石燃料燃烧的共同贡献。在距地表15~34 cm处,柱状剖面层的PAHs含量显著增加,这是由于1987年和1998年大兴安岭发生森林火灾树木燃烧所致。     

Polycyclic aromatic hydrocarbons and their molecular diagnostic ratios in urban atmospheric respirable particulate matter

Atmospheric concentrations of polycyclic aromatic hydrocarbons (PAHs) in Santiago de Chile city were evaluated to study particulate PAHs profiles during cold and spring weather periods. Urban atmospheric particulate matter PM10 was collected using High Volume PM10 samplers. Fifteen samples of 24 h during austral winter and 20 samples of 24 h during spring, 2000 were collected at two sampling sites (North–East and Central areas of the city) whose characteristics were representative of the prevailing conditions. Seventeen PAHs were quantified and total PAHs concentration ranged from 1.39 to 59.98 ng m⁻³, with a seasonal variation (winter vs. spring ratio) from 0.5 to 12.6 ng m⁻³. Molecular diagnostic ratios were used to characterize and identify PAHs emission sources such as combustion and biogenic emissions. Results showed that the major sources of respirable organic aerosol PM10 in Santiago are mobile and stationary ones.     

湖泊疏浚堆场淤泥污染及潜在生态风险评价

疏浚淤泥内通常含有不同类型的有毒有害物质,在堆场直接堆放过程中可能会对周围环境产生有害影响.本文针对太湖及巢湖相应疏浚堆场内淤泥进行研究,探讨淤泥中重金属、多环芳烃以及多氯联苯等污染物含量及潜在生态风险;根据重金属的风险指数法和持久性有机污染物的风险商法,对各污染物的潜在生态风险进行定量分析.研究结果表明,太湖白旄堆场以及孔湾堆场淤泥内重金属及多环芳烃含量较小,潜在生态风险较低;巢湖南庄堆场淤泥内各类有害物质含量较大,种类较多,对于周围环境具有较高的潜在生态威胁.多氯联苯则在各个疏浚堆场淤泥中具有很高的积累量,潜在生态风险较高,应引起管理者的重视.     

Vertical transport of polycyclic aromatic hydrocarbons in different particle-size fractions of sandy soils

Vertical transport of selected polycyclic aromatic hydrocarbons (PAHs) in different particle-size fractions of sandy soils was investigated by simulation experiments in soil columns. Tested soil samples were fractionized into three particle-sizes including sand, coarse silt and fine silt (2,000–50, 50–20 and <20 μm). Rainfall simulations were conducted in artificially PAHs contaminated soil columns with 30 cm length and 5 cm diameter in 40 days. PAHs were extracted from soil samples and determined by high performance liquid chromatography (HPLC). Results showed that the residue level of PAHs in fine silt fraction reached 35.85 mg/kg, which was significantly higher than those in sand and coarse silt fraction (16.28 and 11.80 mg/kg, respectively), probably because PAHs in macroporous fractions were prone to volatilize or degrade compared with that in microporous fractions. Linear relationship between the residue levels of individual PAH (R _PAHs) and the value of partition coefficient (log K _oc) was regressed as R _PAHs = 1.55 × log K _oc − 5.86, R ² = 0.91, n = 9. These results indicated that vertical transport of the mixed PAHs in soils were controlled both by the nature of PAHs (i.e. log K _oc, molecular weight), soil particle size and soil organic contents, which could influence the transport of PAHs.     

Accumulation of copper in the Permian Kupferschiefer: A result of post-depositional redox reactions

Within the Central European Zechstein Basin the Permian Kupferschiefer has been deposited under anoxic conditions. In most parts of the basin, the metal content does not exceed values commonly observed in black shales. However, in areas near to the Zechstein sea-shore which are simultaneously related to rift zones a significant base metal enrichment is observed. Organic geochemical analyses of the copper-mineralized sections in the Kupferschiefer from Southwest Poland show that significant changes in the composition of organic matter are associated with the metal enrichment processes. Porphyrins, commonly abundant constituents of the shale, have been decomposed by oxidizing fluids. Additionally, aliphatic hydrocarbons have been largely removed from the bitumen and alkylated aromatic systems were affected by side-chain degradation. This particular type of alteration is explained by ascending oxidizing solutions which transported high amounts of base metals from Lower Permian red beds into the Kupferschiefer horizon acting as a geochemical trap. The metal precipitation is suggested to be a result of thermochemical sulphide production with organic matter acting as hydrogen source. In areas such as the Lower Rhine Basin in the bottom section of the Kupferschiefer the base metals lead and zinc as well as barium have been accumulated from basinal Carboniferous formation waters. Copper enrichment is not observed because potential source rocks are missing in this area. However, the observed compositional changes of the organic matter do not point towards thermochemical redox processes.     

厦门西海域表层水中PAHs污染与PAHs降解菌分布的关系

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。     

蒽、菲、芘、■混合液对菲律宾蛤仔抗氧化酶活性的影响

以菲律宾蛤仔（Ruditapes philippinarum）为研究对象，在实验生态条件下采用不同浓度的蒽（Fluoranthene）、菲（Phenaphthene）、芘（Pyrene）、[艹屈]（chrysene）混合液进行染毒实验，研究菲律宾蛤仔体内超氧化物歧化酶（superoxide dismutase，SOD）、过氧化氢酶（catalase，CAT）和谷胱苷肽过氧化物酶（glutathione peroxidase，GPx）的剂量-效应关系和时间-效应关系。实验的3种混合液浓度为5μg／L（低浓度组），50μg/L（中浓度组），500μg／L（高浓度组）。结果表明，在低浓度混合液下（5μg／L），CAT比SOD和GPx更快受到诱导；4种多环芳烃混合污染物对SOD、CAT和GPx活性的影响均为先诱导后抑制的变化过程。     

The North Cape oil spill: hydrocarbons in Rhode Island coastal waters and Point Judith Pond.

On 19 January 1996, the North Cape oil barge ran aground near Moonstone Beach, RI, and spilled over 2700 metric tons of No. 2 fuel oil during a severe winter storm. High winds and rough seas drove the oil into the water column, and the oil spread throughout Block Island Sound and into several coastal salt ponds. Over 50 water samples were collected from Point Judith Pond (PJP) and the southern coast of Rhode Island for four months after the spill and analyzed for polycyclic aromatic hydrocarbons (PAHs) and total petroleum hydrocarbons (TPHs). These analyses revealed that at least 60 km2 of coastal waters were impacted from the spill. Maximum concentrations of sigmaPAHs and TPHs were 115 and 3940 microg l(-1), respectively. The percentage of sigmaPAHs relative to the TPHs for all samples varied from 0.2 to 43%, showing that there was no clear relationship between sigmaPAHs and TPHs for the whole dataset and likely resulting from spatial and temporal partitioning over the course of the spill. However, within the dataset, there were stronger correlations for distinct samples collected at similar locations and times. In PJP, water column concentrations of individual PAHs decreased at rates of 0.08-0.24 day(-1) and lower-molecular weight PAHs were removed faster than higher-molecular weight PAHs.     

溴素的有机化学 Ⅳ．单取代苯甲酸多溴代芳酯的合成

报导合成了四种新的单取代苯甲酸多溴代芳酯：４－溴苯甲酸－２＇，４＇，６＇－三溴苯酯，双（４－溴苯甲酸）－２＇，３＇，５＇，６＇－四溴－１＇，４＇－苯二酯，双（４－羟基苯甲酸）－２＇，３＇５＇，６＇－四溴－１＇，４＇－苯二酯和双（２－羟基苯甲酸）－２＇，３＇，５＇，６＇－四溴－１＇，４＇－苯二酯。     

Reconstruction of pollution history of organic contaminants in the upper Gulf of Thailand by using sediment cores: first report from Tropical Asia Core (TACO) project

This paper reports the first reconstruction of a pollution history in tropical Asia from sediment cores. Four sediment core samples were collected from an offshore transect in the upper Gulf of Thailand and were analyzed for organic micropollutants. The cores were dated by measurement of (137)Cs and geochronometric molecular markers (linear alkylbenzenes, LABs; and tetrapropylene-type alkylbenzenes, TABs). Polychlorinated biphenyl (PCB) concentrations showed a subsurface maximum in layers corresponding to the 1970s, indicating the effectiveness of regulation of PCBs in Thailand. LAB concentrations increased over time, indicating the increase in input of sewage into the Gulf during the last 30 years. Hopanes, biomarkers of petroleum pollution, also increased over time, indicating that the inputs of automobile-derived hydrocarbons to the coastal zone has been increasing owing to the increased number of cars in Thailand since the 1950s. Polycyclic aromatic hydrocarbons (PAHs) increased in the layers corresponding to the 1950s and 1960s, probably because of the increased inputs of automobile-derived PAHs. PAH concentrations in the upper layers corresponding to the 1970s and later remained constant or increased. The absence of a subsurface maximum of PAHs contrasts with results observed in industrialized countries. This can be explained by the facts that the Thai economy did not depend on coal as an energy source in the 1960s and that economic growth has continued since the 1970s to the present. The deposition flux of PAHs and hopanes showed a dramatic offshore decrease, whereas that of LABs was uniform.