The effects of interspecific fungal interactions between Trametes versicolor and Phanerochaete chrysosporium on laccase activity and enzymatic oxidation of polycyclic aromatic hydrocarbons(PAHs) were investigated.A deadlock between the two mycelia rather than replacement of one fungus by another was observed on an agar medium.The laccase activity in crude enzyme extracts from interaction zones reached a maximum after a 5-day incubation,which was significantly higher than that from regions of T.versicolor or P.chrysosporium alone.The enhanced induction of laccase activity lasted longer in half nutrition than in normal nutrition.A higher potential to oxidize benzo[a]pyrene by a crude enzyme preparation extracted from the interaction zones was demonstrated.After a 48 hr incubation period,the oxidation of benzo[a]pyrene by crude enzyme extracts from interaction zones reached 26.2%,while only 9.5% of benzo[a]pyrene was oxidized by crude extracts from T.versicolor.The oxidation was promoted by the co-oxidant 2,2'-azinobis-3ethylbenzthiazoline-6-sulphonate diammonium salt(ABTS).These findings indicate that the application of co-culturing of white-rot fungi in bioremediation is a potential ameliorating technique for the restoration of PAH-contaminated soil.
作为斯德哥尔摩公约拟增列名单中的一类化合物,短链氯化石蜡(short chain chlorin-ated paraffins,SCCPs)因其与已知持久性有机污染物的相似性而引起广泛关注.我国作为氯化石蜡(CPs)世界第一大生产国,相关方面的研究报道尚处空白.本文比较了气相色谱-电子捕获检测器(gas chromatograph-electron capture detector,GC-ECD)、气相色谱-低分辨电子捕获负化学离子源质谱(gas chromatograph-electron capture negative ion low resolution mass spectrometry,GC-ECNI-LRMS)及气相色谱-电子轰击串联质谱(gas chromatograph-electron ionization tandem mass spectrometry,GC-EI-MS2)测定CPs的方法,建立了土壤样品CPs总量的分析测定方法,回收率达到82.4%±17.0%,检测限为0.25ng.利用所建立的方法,对我国电子垃圾拆解地土壤中CPs的污染水平进行了初步研究.
Polychlorinated dibenzo-p-dioxins/dibenzofurans(PCDD/Fs) and polychlorinated biphenyls(PCBs) were monitored in a seasonal passive sampling scheme during June 2008 and January 2009 to investigate the spatial concentration,congener profiles and evaluate the potential inhalation risk in different functional areas in Tianjin,China.The spatial air concentrations and I-TEQs ranged 1.08×102-8.19×10 3 fg m-3(average 2.63×103 fg m-3) and 4.08-325 fg I-TEQ m-3(average 91.4 fg I-TEQ m-3) respectively for PCDD/Fs.The concentration and I-TEQs of PCBs were 3.08×104-3.01×105 fg m-3(average 1.39×105 fg m-3) and 1.72-49.6 fg I-TEQ m-3(average 18.5 fg I-TEQ m-3).It is obvious that PCB concentrations were several hundred times higher than the PCDD/Fs.However,the ambient air PCDD/Fs contributed a major part to the total toxicity equivalents,varying from 72.7% to 89.0%(average 81.8%).The atmospheric PCDD/F levels were observed to be higher in winter for most of sampling sites in the downtown.Besides,inhalation risk assessment showed that local residents might suffer more risk near the point sources than those in living area,industrial zones and background area in Tianjin City.However,the total daily dioxin intake was approximately several to hundreds of times lower than the WHO criteria,showing relatively low exposure risks from the impact of industry point sources in Tianjin City.
建立了高效液相色谱-电喷雾串联质谱(HPLC-ESI MS/MS)分析环境水样中22种抗生素类药物的方法。采用HLB固相萃取柱对环境水样中的目标化合物进行富集、净化,然后以6mL氨水-甲醇(5∶95,v/v)溶液洗脱。收集的洗脱液经氮气吹干至1mL,然后进行HPLC-ESI MS/MS分离分析。色谱流动相A相为甲醇-乙腈(1∶1,v/v),B相为0.3%(体积分数)甲酸水溶液(含0.1%(体积分数)甲酸铵,pH2.9);色谱柱为XTerra MS C18柱。质谱检测采用正离子扫描,多反应监测模式。分别以自来水和污水作为基质,22种抗生素类药物的加标平均回收率分别为54.9%～130%和57.4%～138%,相对标准偏差(n=3)分别为2.85%～28.6%和2.02%～23.2%;方法的检出限为0.05～0.5ng/L。将建立的方法应用于北京市高碑店湖和小清河水样的分析,结果表明在两个水样中均有部分抗生素类药物检出。
The indoor total volatile organic compound (TVOC) concentrations and their relationship to potential influencing factors were evaluated. Samples (n = 2302) were collected from 2007 to 2009 both in old structures and new construction in the city of Hangzhou from bedrooms, sitting rooms and studies that had been decorated within the previous year. The average TVOC concentration in all the newly decorated rooms was 0.65±0.69 mg/m 3 . 35.8% of samples exceeded the China standard. Over the past 3 years, the TVOC concentration decreased and then increased (P < 0.05). The percentage of samples exceeding the China standard in the three rooms decreased in the following order: sitting room>study>bedroom. The characteristics of the TVOC source were a key factor influencing the TVOC concentration. In addition, the TVOC concentration was also (P < 0.05) related to the temperature, humidity, time from the end of decoration to sampling (DR), and the amount of time windows and doors were closed before sampling (DC). The temperature and humidity were less important than the DR and DC. A model to relate the TVOC concentration to the five factors (temperature, humidity, source, DR, and DC) was established based on 288 samples (R 2 = 0.83). The model illustrated that the time for the TVOC concentration to meet the China standard was different for the various rooms, and when the other factors were fixed, the impact of DC (t 1 ) on the TVOC concentration could be quantified as (((t 1 +1)/2) 0.212 1)×100%.
LIU Jian LeiBAI GeCHEN JieZHU LiZhongGUO WeiQiangSHEN XueYou
Neuronal toxic pollutants in environment possess hazards to human health. It is essential to determine the causative neuronal toxicants in environmental samples. In the present study, viability of primary cultured cerebellar granule neurons (CGNs), combined with sample extraction, chemical fractionation and identification, was applied for screening acid-resistant neuronal toxic substances in environmental samples. River sediments and agricultural soils along the river near a brominated flame retardant (BFR) manufacturing plant in South China were collected to screen the key neuronal toxicants. The results indicated that the manufacturing plant was a source of neuronal toxicity risks. In the sediment and soil near the plant, one of the causative toxicants was identified as tris-(2,3-dibromopropyl) isocyanurate (TBC) using HPLC-MS/MS. In addition, an unknown chemical possibly causing significant neuronal toxicity was isolated from all the soil samples in the region.
QU GuangBo, SHI JianBo, LI ZhuoNa, RUAN Ting, FU JianJie, WANG Pu, WANG Thanh & JIANG GuiBin * State Key Laboratory of Environmental Chemistry and Ecotoxicology
The concentrations and species of organotin compounds(OTCs) in 52 surface sediment samples from nine fishing ports along the Chinese coast were studied.Butyltins(BTs) and phenyltins(PhTs) were derivatized using sodium tetraethylborate(NaBEt 4) and determined by head-space solid-phase microextraction(HS-SPME) gas chromatography coupled with a flame photometric detector(GC-FPD).The concentrations of OTCs ranged from <3.6 to 194 ng(Sn) g-1 dry weight(dw) for monobutyltin(MBT),<2.3 to 41.5 ng(Sn) g-1 dw for dibutyltin(DBT),<0.7 to 86.0 ng(Sn) g-1 dw for tributyltin(TBT) and <5.1 to 66.1 ng(Sn) g-1 dw for monophenyltin(MPhT),respectively.The concentrations of diphenyltin(DPhT) and triphenyltin(TPhT) were below the limit of detection(LOD).BTs were the main species in the sediments except for the samples collected from Shazikou fishing port in Qingdao.The concentrations of MBT were higher than DBT and TBT.The concentrations of OTCs in the sediments varied widely among different sampling locations.The concentrations of BTs were much higher in the samples collected from fishing ports close to the South China Sea than those in coast of the East China Sea and the Yellow Sea.MPhT was prevalent in most sampling stations except for those in coast of the East China Sea.The environmental and ecotoxicological risks of TBT in most sediment samples were low.
