杭州市城市和郊区表土磷库及环境风险评价

杭州市城市和郊区土壤磷素具有明显的积累特征并有较高的潜在释放能力。可提取态P(包括H2O-P、NaHCO3-P.NaOH-P和HCl-P)平均在80％左右，其中以HCl—P的比例最高，平均约55％。32个研究土样中，26个土样的水可溶性(H20—P)在10mg／kg以上，15个土样的NaHCO3—P在100mg/kg以上。酸性条件下P的释放潜力明显增加。土壤水溶性P含量及在酸性条件下P的释放量与土壤总P呈正相关，与土壤pH负相关。     

The nature and significance of public exposure to arsenic: a review of its relevance to South West England

In South West England, more than two hundred years of intensive exploitation of metalliferous ore deposits, combined with the natural processes of pedogenesis from mineral-rich parent rocks, has resulted in the creation of a aignificant area of arsenic-contaminated wastes and soils. The scale of arsenic dispersion by natural and anthropogenic processes is such that 722 km² of land contains concentrations of arsenic in excess of 110 g g^–1, more than twice the maximum that might be expected in a normal soil.The general rationale for the clean-up of derelict and contaminated mining sites often includes aesthetic factors and the desirability of preventing the dispersion of contaminants beyond the site boundaries. Only in extreme cases is public health directly invoked as justification for remediation. In South West England, if arsenic constitutes a genuine threat to the public, an increased rate of site remediation would be justified. The primary purpose of this review is to establish whether or not widespread arsenic contamination (principally of soils) has any measurable effects on public health in South West England, and how this might affect current contaminated site remediation policy. The review is based on data from previous research in the region, and other relevant international studies of mining and smelting communities, and other populations exposed to elevated arsenic concentrations. The literature reviewed also includes the determination of the extent and sources of contamination, and pathways between source and man.While the contamination of potable waters in some countries has led to measurable health effects, this scenario has not yet been identified in South West England, and there is little reason to believe that significantly contaminated potable water supplies would escape detection for extended periods of time under the current monitoring regime.In relative terms (based on both globaland local data), one of the most significant links between contaminated soils and humans appears to be contaminated food stuffs. In absolute terms, such exposure is low due to the natural constraints on arsenic uptake by herbage, cereal crops and vegetables, and the food chain does not appear to have been significantly compromised in South West England. Chronic health effects are unlikely as excessive arsenic concentrations in locally grown food crops remain rare.With the problems of confounding medical and social factors, it is not surprising that studies in South West England have failed to identify chronic exposure to arsenic at very low concentrations as a significant health risk. Those studies that indicate otherwise do not stand up to close scrutiny. It appears that the number of additional deaths arising from the widespread arsenic contamination in South West England is small. The relative benefits of a costly statistical study to actually determine the number of additional deaths might be considered minimal, but one major area could benefit from further studies: the sensitivity of certain population sub-groups to environmental arsenic exposure. Of particular interest are children, for whom significant exposure to arsenic via soil ingestion may be occurring.Based on available information, there appears to be no justification for a large programme of site remediation. Resources should, however, be expended on enlightening the general public, and private and governmental organisations as regards the gap between the perceived and actual significance of arsenic contamination in South West England.To whom correspondence should be addressed.     

A Preliminary Study of Geographic Influence on Arsenic Concentrations in Human Hair

Past mining activities in the county of Cornwall in the United Kingdom, has exposed the local environment to raised levels of As. Previous research has shown an increased concentration of As in crops grown in such areas and the subsequent take-up of As through the food chain may lead to an increased body burden in man. In an attempt to evaluate this, a pilot study was carried out using Particle Induced X-ray Emission to compare the hair As concentration of a group of Cornish residents to that of a control group consisting of residents in the counties of Oxfordshire and Wiltshire. The null hypothesis being that there is no significant difference between the hair As concentrations of the two groups.Each group comprised thirty six age and sex matched subjects. The mean hair As concentration for the Cornish group was 2.51 g g-1, which is significantly greater than that of 0.7 g g-1 found in the control group (p = 0.004). The World Health Organisation suggests a hair As value greater than 1 g g-1 as evidence of increased exposure to As and 5 g g-1 is quoted by the Canadian Government as evidence of significant ingestion of As. Twenty one Cornish subjects registered a value at or above 1 g As g-1 compared to nine in the control group (p = 0.0003). Five subjects in the Cornish group had values that exceed 5 g As g-1, compared to only two in the control group (p = 0.23). We use the results of this study as evidence to support our continued work in this area in order to evaluate possible health implications.     

用连续提取法研究芘在鱼鳃表面的结合形态

建立了研究鱼鳃表面芘的结合状态的四步连续提取方法．分别用H2O、CaCl2、CH3OH和n-C6H14+CH2Cl2(1:1, v/v)混合液提取经暴露的鱼鳃．操作定义的前3步分别提取松散附着在鳃表的鱼鳃黏液中的芘,紧密附着在鳃表的鱼鳃黏液中的芘以及直接吸着在鱼鳃表皮上的芘,第4步则用来提取鱼鳃组织吸收的芘．其提取的芘分别占总量的 4．0％、12．1％、45．2％和38．7％．经3 h暴露,进入鳃组织的芘仅为总测定量的三分之一强,因此大部分芘并未进入鳃组织．单独进行的五步CH3OH连续提取实验结果证明,CH3OH提取步骤能有效地解吸鳃表吸着的芘,但不会导致鳃组织中芘的释放．动态实验结果表明,黏液结合态芘在暴露1h左右即达到平衡,而鳃表吸着态和鳃组织吸收态芘在暴露3h内含量迅速上升,3 h后显著趋缓．     

Temporal dynamics of arsenic uptake and distribution: food and water risks in the Bengal basin

Abstract

Contaminated food chain is a serious contender for arsenic (As) uptake around the globe. In Nadia, West Bengal, we trace possible means of transfer of As from multiple sources reaching different trophic levels, and associated seasonal variability leading to chronic As uptake. This work considers possible sources-pathways of As transfer through food chain in rural community. Arsenic concentration in groundwater, soil, rice, and vegetable-samples collected detected in different harvest seasons of 2014 and 2016. Arsenic level in shallow groundwater samples ranged from 0.1 to 354?µg/L, with 75% of the sites above the prescribed limit by WHO (10?µg/L) during the boro harvest season. High soil As content (～20.6?mg/kg), resulted in accumulation of As in food crops. A positive correlation in As conc. with increase over period in all sites indicating gradual As accumulation in topsoil. Unpolished rice samples showed high As content (～1.75?mg/kg), polishing reduced 80% of As. Among vegetables, the plant family Poaceae with high irrigation requirements and Solanaceae retaining high moisture, have the highest levels of As. Contaminated animal fodder (Poaceae) and turf water for cattle are shown to contaminate milk (0.06 to 0.24?µg/L) and behoves strategies, practices to minimize As exposure.     

污染场地总石油类馏分分段法风险评估

在对某汽车工业污染场地开展土壤与地下水环境调查的基础上,根据《污染场地风险评估技术导则》中的推荐模型,采用馏分分段法对总石油类进行风险评估研究。结果表明,1)该场地主要污染物为总石油类,土壤污染物中C12~C16脂肪烃的非致癌危害商在敏感用地和非敏感用地两种用地方式下均大于1,地下水污染物中C8~C10脂肪烃、C12~C16脂肪烃、C16~C21脂肪烃、C21~C34脂肪烃、C21~C35芳香烃的非致癌危害商在两种用地方式下均远大于1;2)敏感用地方式下,土壤中总石油类的修复限值为1 023.92mg/kg,地下水中总石油类的修复限值为1.805 mg/L;3)非敏感用地方式下,土壤中总石油类修复限值为3 292.92 mg/kg,地下水中总石油类的修复限值为11.457 mg/L。     

Organic matter extracted from activated sludge with ammonium hydroxide and its characterization

In order to characterize the organic properties of waste activated sludge in a wastewater treatment plant,organic matter within sludge was extracted with NH 3 ·H 2 O preferentially,and subsequently fractionated into five fractions using XAD-8/XAD-4 resins.Up to a 63.8%-71.1% of organic matter within the sludge could be efficiently extracted by NH 3 ·H 2 O.Fractionation results showed that hydrophobic acid and hydrophilic fraction were two main components among the sludge organic matter (accounting for 32.2% and 48.0% of the bulk organic matter,respectively),whereas transphilic acid,hydrophobic neutral and transphilic neutral were quite low (accounting for 9.2%,5.8% and 4.8%,respectively).Despite that the extractant of NH 3 ·H 2 O showed a relatively higher extraction efficiency of the aromatic components,the relatively low aromaticity of the organic fractions implied that those non-aromatic components could also be effectively extracted,especially for neutral and hydrophilic fractions.In addition,acidic fractions contained more aromatic humic-like components,whereas the neutral fractions had a greater content of aromatic proteins and soluble microbial byproduct-like components.Extraction of sludge organics with NH 3 ·H 2 O and subsequential fractionation using XAD resins could be a novel method for further characterization of sludge organics.     

基于批式呼吸计量法的溶解性COD组分划分

利用批式好氧呼吸计量法结合溶解性慢速水解COD(S_H)水解动力学拟合提出了溶解性COD(SCOD)的组分划分方案.上海2个污水处理厂进水的SCOD组分划分结果表明,A厂沉砂池出水(典型生活污水)的SCOD中含有43.5%～58.6% S_H、 21.8%～35.2%易生物降解COD(S_S)和15.4%～30.9%溶解性惰性COD(S_I); B厂沉砂池出水(长距离输送的合流制污水)SCOD中含有34.5%～45.2% S_H、 29.3%～37.7% S_S和25.6%～31.2% S_I. 9组不同水样的试验拟合结果表明,一级动力学能够很好地描述S_H的水解过程,A厂和B厂进水S_H的水解速率常数分别为28.00～39.77 d^-1和26.48～29.52 d^-1.该组分划分方案能够实现S_S积分区域的理论划分,并消除溶解性微生物产物对S_I测定的影响.     

The role of phosphorus in the metabolism of arsenate by a freshwater green alga, Chlorella vulgaris

A freshwater microalga, Chlorella vulgaris, was grown in the presence of varying phosphate concentrations( 10–500 μg/L P) and environmentally realistic concentrations of arsenate(As(Ⅴ))(5–50 μg/L As). Arsenic speciation in the culture medium and total cellular arsenic were measured using AEC-ICP-MS and ICP-DRC-MS, respectively, to determine arsenic biotransformation and uptake in the various phosphorus scenarios. At high phosphate concentration in the culture medium, 100 μg/L P, the uptake and biotransformation of As(Ⅴ) was minimal and dimethylarsonate(DMAs(Ⅴ)) was the dominant metabolite excreted by C. vulgaris, albeit at relatively low concentrations. At common environmental P concentrations, 0–50 μg/L P, the uptake and biotransformation of As(Ⅴ) increased. At these higher As-uptake levels, arsenite(As(Ⅲ)) was the predominant metabolite excreted from the cell. The concentrations of As(Ⅲ) in these low P conditions were much higher than the concentrations of methylated arsenicals observed at the various P concentrations studied. The switchover threshold between the(small) methylation and(large) reduction of As(Ⅴ) occurred around a cellular As concentration of 1 fg/cell. The observed nearly quantitative conversion of As(Ⅴ) to As(Ⅲ) under low phosphate conditions indicates the importance of As(Ⅴ) bio-reduction at common freshwater P concentrations. These findings on the influence of phosphorus on arsenic uptake, accumulation and excretion are discussed in relation to previously published research. The impact that the two scenarios of As(Ⅴ) metabolism, As(Ⅲ) excretion at high As(Ⅴ)-uptake and methylarsenical excretion at low As(Ⅴ)-uptake, have on freshwater arsenic speciation is discussed.     

Thiolated arsenicals in arsenic metabolism: Occurrence, formation, and biological implications

Arsenic (As) is a notoriously toxic pollutant of health concern worldwide with potential risk of cancer induction, but meanwhile it is used as medicines for the treatment of different conditions including hematological cancers. Arsenic can undergo extensive metabolism in biological systems, and both toxicological and therapeutic effects of arsenic compounds are closely related to their metabolism. Recent studies have identified methylated thioarsenicals as a new class of arsenic metabolites in biological systems after exposure of inorganic and organic arsenicals, including arsenite, dimethylarsinic acid (DMAV), dimethylarsinous glutathione (DMAIIIGS), and arsenosugars. The increasing detection of thiolated arsenicals, including monomethylmonothioarsonic acid (MMMTAV), dimethylmonothioarsinic acid (DMMTAV) and its glutathione conjugate (DMMTAVGS), and dimethyldithioarsinic acid (DMDTAV) suggests that thioarsenicals may be important metabolites and play important roles in arsenic toxicity and therapeutic effects. Here we summarized the reported occurrence of thioarsenicals in biological systems, the possible formation pathways of thioarsenicals, and their toxicity, and discussed the biological implications of thioarsenicals on arsenic metabolism, toxicity, and therapeutic effects.