Mechanistic aspects of the thermal formation of halogenated organic compounds including polychlorinated dibenzo‐p‐dioxins. Part V†: Hypotheses and summary

The hypotheses on the de novo syntheses of polychlorinated dibenzofurans (PCDFs) and polychlorinated dibenzo‐p‐dioxins (PCDDs), based on known literature, are presented. Polychlorinated benzenes and polychlorinated phenols are probably key intermediates.

In the present article, hypotheses that may account for the presence of polychlorinated dibenzofurans (PCDFs) and dibenzo‐p‐dioxins (PCDDs) in the effluents from municipal and industrial incinerators are put forward. These hypotheses are based on the previously surveyed literature (Ref. 203–206) and experimental results on laboratory scale and thermodynamic calculations are considered. The interconnections of various reaction steps are speculative and no technological information was added to account for conditions in real incinerators. Conclusion of the discussions on the related subject matter, presented in the Parts I‐IV (Ref. 203–206), are also described in this paper.     

The use of the embryo‐culture techniques in the research on the Teratogenic and Mutagenic properties of metals†

Actually, embryos can be cultured from the one‐cell stage up to the blastocyst stage, and their development can be easily monitored at any time: severe effects caused by toxic compounds are traduced by rapid embryonic death, less pronounced effects can be expressed by a lowered cleavage activity or by an arrest of the development from a particular stage. The system can be improved by transferring the embryos at the blastocyst stage in another more complete medium where they can “implant”; and form an inner cell mass with differentiated ectoderm and endoderm. Since last years, it has also become possible to culture postimplantation rodent embryos for short periods involving a number of particularly critical stages of organogenesis, such as the formation and closure of the anterior neuropore. Embryo‐culture also represents a useful system to study cytogenetic effects of chemicals which are often linked to lethal or teratogenic effects. These different possibilities are illustrated by examples of studies already performed with metals, and dealing with their teratogenic and/or cytogenetic effects on pre‐ and postimplantation rodents.     

Essential and nonessential elements in the red-crowned crane Grus japonensis of Zhalong Wetland,northeastern China

The concentrations of four essential (Ca, Mg, Zn, and Cu) and two nonessential elements (Pb and Cd) in feathers and kidneys, livers, gut walls, and muscles of eight carcasses of migratory red-crowned cranes (Grus japonensis) from Zhalong Wetland, northeastern China, were examined. The concentrations of Cd in the feathers were between 0.4 mg kg^?1 dry weight (dw) and 3.1 mg kg^?1 dw, in the livers between 0.4 and 4.4 mg kg^?1 dw, the maximum of which exceeded a level considered to be environmental exposure risk (i.e., 3 mg kg^?1 dw in the liver or kidney). High Pb levels (0.4–3.2 mg kg^?1 dw, with an average of 1.8 mg kg^?1) were also detected in livers, which exceeded a level considered toxicosis in birds (1.7 mg kg^?1 dw). Pb and Cd had the highest scores in principal component analysis. Relatively high Pb and Cd concentrations in the migratory cranes were thought to be associated with their habitat and prey.     

1980—2007年我国燃煤大气汞、铅、砷排放趋势分析

基于文献调研,对1980—2007年我国汞、铅、砷3种主要燃煤大气重金属排放清单进行归纳,计算了3种重金属的逐年平均排放量,并分析排放量与燃煤量的相关性、单位煤耗大气重金属污染物排放量的变化趋势及原因. 结果表明:1980—2007年我国燃煤大气汞、铅、砷排放量与燃煤量增长趋势基本一致,均呈显著正相关(R2分别为0.911、0.971、0.996),但燃煤大气汞排放量与燃煤量间的相关性却比铅、砷排放量与燃煤量的相关性小很多,这主要是燃煤电厂对汞协同脱除能力比对铅、砷强,以及电厂汞排放所占比例较大所致. 燃煤大气汞排放量在2005年后趋于稳定,而铅、砷排放量在2000年后快速增长,年均增速均超过10%,其中电厂和工业锅炉是重金属排放的重点行业. 在燃煤量不断增长的背景下,单位煤耗的大气汞、铅排放量均呈下降趋势,其中汞排放量在2005—2007年年均降低5.0%,铅排放量在1996—2007年年均降低1.7%. 这与我国主要燃煤行业除尘、脱硫、脱硝等大气污染控制装置对重金属的协同脱除能力不断增强有密切关系.      

铅对赤子爱胜蚓抗氧化酶活性的影响

研究了老化和未经老化土壤中Pb(NO₃)₂对赤子爱胜蚓(Eisenia fetida)体内SOD(超氧化物歧化酶)、CAT(过氧化氢酶)、POD(过氧化物酶)活性的影响. 结果表明:在测试范围(w〔Pb(NO₃)₂〕为200~1000 mg/kg)内,Pb(NO₃)₂对蚯蚓体内3种抗氧化酶的活性均有显著性影响. 暴露于未经老化土壤1、14、21d时,蚯蚓体内SOD和CAT活性均随土壤中w〔Pb(NO₃)₂〕的增加而降低,高w〔Pb(NO₃)₂〕下,与对照组相比这2种抗氧化酶活性均降低了约40%. POD活性除第1、3天在高w〔Pb(NO₃)₂〕中显著变化外,其他暴露时间、暴露水平中均无显著性变化. 暴露于老化(28d)土壤1d后,蚯蚓体内SOD、POD、CAT活性均随土壤中w〔Pb(NO₃)₂〕的增加而升高,高w〔Pb(NO₃)₂〕下,与对照组相比这3种抗氧化酶活性分别升高了359%、147%和233%;然而,随着暴露时间的延长,3种抗氧化酶活性又呈显著降低趋势. 总体上,蚯蚓体内CAT和SOD活性变化趋势基本一致. 研究显示,土壤老化对铅毒性产生了影响,因此在进行毒性试验时应予以考虑.      

中国浏阳农村地区人群暴露参数

以湖南省浏阳市农村地区人群为研究对象,采用问卷调查的方式对研究地区人群的暴露参数进行研究,结果表明:研究地区成人男性、女性的平均体质量分别为62.45和53.71kg,平均体表面积分别为1.710和1.546m2;成人日均饮水摄入量为1428 mL,P₉₅(第95百分位数)为3350mL,其中,日均直接饮水量为1035mL,P₉₅为2500mL;调查地区大米、面粉、鱼类、猪肉、鸡肉、蛋类(鸡蛋和鸭蛋合计)日均摄入量,成人男性为335.54、89.28、15.41、18.48、14.18和21.70g/d,成人女性为269.28、68.45、14.89、16.73、13.11和18.07g/d. 研究还发现,调查地区人群饮用水源以泉水和井水为主,分别占52.42%和36.31%,也有个别人群饮用河水和湖水等地表水. 研究结果与美国和日本暴露参数推荐值相比有较大差异,与我国同类研究相比也存在一定的差异,说明暴露参数具有区域性、种族性等特征.      

Preliminary Evaluation of the Use of Phosphogypsum for Reef Substrate. I. A Laboratory Study of Bioaccumulation of Radium and Six Heavy Metals in an Aquatic Food Chain

Phosphogypsum (PG), a solid by-product of phosphoric acid production, contains radionuclides and trace metals in concentrations which may pose a potential hazard to human health and the environment. to investigate the possibility of bioaccumulation of radium and six heavy metals over time when aquatic organisms experience both trophic and environmental exposure to PG, we designed a laboratory experiment representing three levels of an aquatic food chain. During the 135 day experiment, a meiobenthic copepod species (Amphiascoides atopus) was cultured in the presence of PG. the copepods were subsequently fed to grass shrimp (Palaemonetes vulgaris and P. pugio) which were in turn fed to gulf killifish (Fundulus grandis); both the grass shrimp and the killifish also experienced an environmental PG exposure. Other than elevated radium levels in the experimental grass shrimp, the experiment demonstrated little effect of environmental or trophic exposure to PG on microinvertebrates, macroinvertebrates, or fishes that could be attributed to PG. in all cases where increased concentrations were indicated within the experimental group, roughly equivalent increases in metal concentrations also occurred in the control group.     

沿海和内陆地区居民汞暴露量对比

通过对沿海和内陆居民食用水产品消费情况调查以及居民头发汞含量的分析,对不同地区普通居民的汞暴露水平进行了对比研究.居民水产品的消费情况采用调查问卷的形式,对沿海地区大连和内陆地区河南两地普通居民进行了随机调查,并同时采集被调查者的头发作为汞暴露情况的生物样本.本次研究共收集到有效调查问卷及头发样本213份(大连112份;河南101份),两地居民水产品消费量分别为:大连104 g.d-1,河南74 g.d-1;收集到的头发样本采用DMA-80测汞仪(按美国EPA-7473的方法)进行总汞含量的测定.头发总汞含量分析结果显示,大连为(0.363±0.256)μg.g-1,河南地区为(0.192±0.167)μg.g-1.两地区对同一年龄段居民发汞水平比较发现,大连地区居民发汞水平明显高于河南地区.以美国环境保护署(EPA)参考剂量1μg.g-1作为发汞基准,大连地区的超出比例为3%,河南地区的超出比例为1%.该研究结果为了解我国普通居民的汞暴露情况以及后续的汞暴露风险的定量计算提供了基础数据.     

改性柚子皮吸附剂对模拟废水中Pb^2＋的吸附性能

以废柚子皮为原料,经ZnCl2浸泡一加热的化学改性手段制备改性柚子皮生物吸附剂,并通过模拟试验研究该吸附剂对废水中Pb^2＋的去除。考察了模拟废水的pH、吸附时间、吸附剂用量和Pb^2＋初始浓度、温度等因素对柚子皮吸附剂去除Pb^2＋的影响,并研究柚子皮吸附剂对Pb^2＋的吸附动力学及吸附特征。结果表明,模拟废水的pH、吸附时间、吸附剂用量和Pb^2＋初始浓度、温度等因素对柚子皮吸附剂吸附废水中Pb^2＋均有显著影响。适宜的吸附条件为pH5．3-6．5,吸附时间1．5h,吸附剂用量10g·L^-1,Pb^2＋初始质量浓度100mg·L^-1,温度30℃。在该条件下,废水中Pb^2＋去除率在90％以上。柚子皮吸附剂对废水中Pb^2＋的吸附符合动力学二级反应方程,等温吸附规律可用Langmuir、Freundlich和Temkin模型进行较好的描述。     

Competitive adsorption and desorption of copper and lead in some soil of North China

The competitive adsorption and desorption of Pb(II) and Cu(II) ions in the soil of three sites in North China were investigated using single and binary metal solutions with 0.01 mol·L^-1 CaCl₂ as background electrolyte. The desorption isotherms of Pb(II) and Cu(II) were similar to the adsorption isotherms, which can be fitted well by Freundlich equation (R₂>0.96). The soil in the three sites had greater sorption capacities for Pb(II) than Cu(II), which was affected strongly by the soil characteristics. In the binary metal solution containing 1∶1 molar ratio of Pb(II) and Cu(II), the total amount of Pb(II) and Cu(II) adsorption was affected by the simultaneous presence of the two metal ions, indicating the existence of adsorption competition between the two metal ions. Fourier transform infrared (FT-IR) spectroscopy was used to investigate the interaction between soil and metal ions, and the results revealed that the carboxyl and hydroxyl groups in the soil were the main binding sites of metal ions.