挥发性有机物(VOCs)的不同化学去除途径:城市与区域站点的对比

VOCs在大气中主要是与OH自由基、NO₃自由基和O₃等反应氧化去除,部分OVOCs的自身光解也是重要的化学去除途径.本研究基于2018年和2019年秋季在珠三角地区的城市和区域站点的外场观测实验,使用VOCs、常规痕量气体及气象参数的观测数据,对烷烃、烯烃、芳香烃和OVOCs等VOCs组分不同化学去除途径的去除速率进行分析.结果表明,烷烃和芳香烃主要通过与OH自由基反应去除,最高占比超过99%.与NO₃自由基和O₃的反应可贡献烯烃去除速率的80%以上,特别是一些天然源的烯烃(如单萜烯)与NO₃自由基的氧化去除是贡献最大的氧化途径.光解是甲醛最重要的去除途径,在两个站点均达到了50%以上,酮类的光解贡献会高于其他OVOCs类物质.OH自由基的氧化去除途径在城市和区域站点的人为源及天然源VOCs去除中占主导地位.区域站点,烯烃尤其是天然源的烯烃物种,与NO₃自由基和O₃反应的贡献要高于城市站点.本研究对促进不同VOCs物种在大气中的去除...     

Positive Feedback Loop between Introductions of Non‐Native Marine Species and Cultivation of Oysters in Europe

With globalization, agriculture and aquaculture activities are increasingly affected by diseases that are spread through movement of crops and stock. Such movements are also associated with the introduction of non‐native species via hitchhiking individual organisms. The oyster industry, one of the most important forms of marine aquaculture, embodies these issues. In Europe disease outbreaks affecting cultivated populations of the naturalized oyster Crassostrea gigas caused a major disruption of production in the late 1960s and early 1970s. Mitigation procedures involved massive imports of stock from the species’ native range in the northwestern Pacific from 1971 to 1977. We assessed the role stock imports played in the introduction of non‐native marine species (including pathogens) from the northwestern Pacific to Europe through a methodological and critical appraisal of record data. The discovery rate of non‐native species (a proxy for the introduction rate) from 1966 to 2012 suggests a continuous vector activity over the entire period. Disease outbreaks that have been affecting oyster production since 2008 may be a result of imports from the northwestern Pacific, and such imports are again being considered as an answer to the crisis. Although successful as a remedy in the short and medium terms, such translocations may bring new diseases that may trigger yet more imports (self‐reinforcing or positive feedback loop) and lead to the introduction of more hitchhikers. Although there is a legal framework to prevent or reduce these introductions, existing procedures should be improved. Ciclo de Retroalimentación Positiva entre la Introducción de Especies Marinas No‐Nativas y el Cultivo de Ostras en Europa     

废水处理中的非传统脱氮途径

根据实验室小型SBR试验的结果，证实存在其它不同于传统的硝化和反硝化的脱氮途径。结合近几年来在生物脱氮理论方面新的研究进展，指出研究非传统脱氮途径的必要性和重要性，其中很有必要的一项工作是需对硝化、反硝化和脱氮过程作出明确的定义。     

Molarity provides better clarity – using molar-based data when evaluating chlorinated volatile organic compound impacted sites

Abstract

Chlorinated volatile organic compounds are common constituents observed at many contaminated groundwater sites. Common industry practice has been to measure these constituents in groundwater on a weight concentration basis (e.g. µg/l, mg/l). This paper highlights the use of molar-based concentrations, especially in the case of parent-daughter degradation sequences commonly observed with the chloroethene, chloroethane, and chloromethane families of compounds. Converting to molar-based concentrations provides the practitioner greater insight into groundwater plume behavior including better evaluation of degradation processes, remedial progress, possible commingling, and/or sourcing. For example, this paper provides a tank analogy to evaluate whether the commonly misinterpreted observation of “DCE-stall” may be occurring at a site. Multiple examples of the benefits of using molar-based concentration data are also summarized in a project case study presented herein. As demonstrated in this paper, molarity does provide better clarity and can be a powerful evaluation tool in the groundwater practitioner’s toolbox.     

A new approach to graphical and numerical analysis of links between plant chemotaxonomy and secondary metabolism from HPLC data smoothed by a simplex mixture design

Summary. HPLC analysis of secondary metabolites represents an efficient tool for the studying of plant chemical diversity under different aspects: chemotaxonomy, metabolomics, adaptative responses to ecological factors, etc. Statistical analyses of HPLC databases, e.g. correlation analysis between HPLC peaks, can reliably provide information on the similarity/dissimilarity degrees between the chemical compounds. The similarities, corresponding to positive correlations, can be interpreted in terms of analogies between chemical structures, synchronic metabolisms or co-evolution of two compounds under certain environment conditions, etc. . In terms of metabolism, positive correlations can translate precursor-product relationships between compounds; negative correlations can be indicative of competitive processes between two compounds for a common precursor(s), enzyme(s) or substrate(s). Furthermore, the correlation analysis under a metabolic aspect can help to understand the biochemical origins of an observed polymorphism in a plant species. With the aim of showing this, we present a new approach based on a simplex mixture design, Scheffé matrix, which provides a correlation network making it possible to graphically visualise and to numerically model the metabolic trends between HPLC peaks. The principle of the approach consisted in mixing individual HPLC profiles representative of different phenotypes, then from a complete mixture set, a series of average profiles were calculated to provide a new database with a small variability. Several iterations of the mixture design provided a smoothed final database from which the relationships between the secondary metabolites were graphically and numerically analysed. These relationships were scale-dependent, namely either deterministic or systematic: the first consisted of a monotonic global trend covering the whole variation field of each metabolites’ pair; the second consisted of repetitive monotonic variations which gradually attenuated or intensified along a global trend. This new metabolomic approach was illustrated from 404 individual plants of Astragalus caprinus (Leguminoseae), belonging to four chemical phenotypes (chemotypes) on the basis of flavonoids analysed in their leaves. After smoothing, the relationships between flavonoids were numerically fitted using linear or polynomial models; therefore the co-response coefficients were easily interpreted in terms of metabolic affinities or competitions between flavonoids which would be responsible of the observed chemical polymorphism (the four chemotypes). The statistical validation of the approach was carried out by comparing Pearson correlations to Spearman correlations calculated from the smoothed and the crude HPLC database, respectively. Moreover, the signs of the smoothed relationships were finely supported by analogies and differences between the chemical structures of flavonoids, leading to fluent interpretation in relation to the pathway architecture.     

Lack of theoretical basis for predicting rate and pathways of recovery

An inadequate basis for precisely predicting the outcome of lotic ecosystem recovery, whether due to unaided natural processes or management techniques or both, exists because: (1) the field of ecology has not yet matured as a rigorous predictive science; (2) the precise sequence of events, including climatic occurrences, affecting the recovery process may be unique events and thus rarely or never repeated; and (3) even when attempts are made to control the recolonization process through introduction of species, etc., the interaction of these species may not follow deterministic models. Although this symposium focuses on lotic ecosystems, such systems are influenced strongly by exports from the surrounding land mass and, under certain circumstances, this may be the overriding influence on the recovery process; therefore, unless the boundary conditions are determined realistically, the recovery process may not follow desirable pathways. Despite the lack of a robust theoretical support base for lotic ecosystem recovery, some remarkable and rapid recoveries have occurred to either a close approximation of the original condition or to a condition ecologically superior to the damaged condition. In some cases, the recovery was due entirely to natural processes and, in others, often followed relatively straightforward management practices. There is evidence indicating that lotic ecosystem restoration is both cost effective and likely to produce satisfying results relatively rapidly. It is both fortunate that this is the case, since society is likely to support such efforts when the results have been extraordinarily successful, and unfortunate since restoration ecology needs a predictive capability.     

Degradation of diuron in aqueous solution by ozonation

Degradation of diuron [3-(3,4-dichlorophenyl)-1,1-dimethylurea] in aqueous solution and the proposed degradation mechanism of diuron by ozonation were investigated. The factors that affect the degradation efficiency of diuron were examined. The generated inorganic ions and organic acids during the ozonation process were detected. Total organic carbon removal rate and the amount of the released Cl^? increased with increasing ozonation time, but only 80.0% of the maximum theoretical concentration of Cl^? at total mineralization was detected when initial diuron concentration was 13.8 mg L^?1. For N species, the final concentrations of NO₃ ^? and NH₄ ⁺ after 60 min of reaction time were 0.28 and 0.19 mg L^?1, respectively. The generated acetic acid, formic acid and oxalic acid were detected during the reaction process. The main degradation pathway of diuron by ozonation involved a series of dechlorination-hydroxylation, dealkylation and oxidative opening of the aromatic ring processes, leading to small organic species and inorganic species. The degradation efficiency of diuron increased with decreasing initial diuron concentration. Higher pH value, more ozone dosage, additive Na₂CO₃, additive NaHCO₃ and additive H₂O₂ were all advantageous to improve the degradation efficiency of diuron.     

环境中多溴联苯醚(PBDEs)的代谢转化研究现状

多溴联苯醚(PBDEs)作为一种溴系阻燃剂(BFRs),在多种环境介质和生物体内广泛存在且浓度逐年增加,因而越来越多地受到研究者关注.综合PBDEs各方面研究报道,认为其在环境中存在生物和非生物两种转化方式.非生物转化主要是光降解,即PBDEs在光照条件下可通过自由基反应脱溴生成低溴同系物及多溴联苯呋喃(PBDFs).生物转化则包括微生物转化、生物体内转化和生物体外代谢,其转化代谢途径除脱溴外,还有醚键断裂、羟基化和羟基化/脱溴等.对PBDEs在环境中不同转化方式的转化速率、转化途径和转化产物等的研究现状进行综述,对今后PBDEs在环境中归趋、生态风险和健康评价研究将起到一定的指导作用.     

典型氯碱污染场地环境风险评价

以广东某氯碱化工污染场地为研究区域,采集了场地22个土壤及地下水样品,分析了25项污染物在不同区域的分布特征及其来源。监测结果表明,煤炭堆场与锅炉房区土壤受重金属铅、镍污染。六六六、四氯化碳、三氯甲烷、六氯苯、苯是场地的特征污染物,主要分布在危险品仓库、漂洗车间与四氯化碳车间。根据监测结果开展了不同暴露途径致癌风险值及非致癌危害商的计算。结果表明,部分样品表层土壤中上述有机污染物的基于人体健康致癌风险指数均超过10-6,最高达到1.65×10-2,表明风险水平高;非致癌危害在各暴露途径下也超过可接受值1,最高达5.59×104,表明风险水平高。说明对于存在高风险的区域必须进行采取合适的措施进行修复,减缓场地再利用后对人群健康的影响。     

Degradation of tert-butyl formate and its intermediates by an ozone/UV process

In this paper, the oxidation of tert-butyl formate (TBF) in aqueous solution by an ozone/UV process was described. The oxidation process was investigated experimentally in a semibatch reactor. The results of the study indicated that the ozone/UV process was very effective in oxidizing TBF. tert-Butyl alcohol (TBA), hydroxy-iso-butyraldehyde (HiBA), acetone, formaldehyde, and formic acid were identified as major primary intermediates during the oxidation of TBF. About 90% organic carbon balance was obtained indicating that most reaction intermediates have been identified and quantified. Some of the primary intermediates were also oxidized in the ozone/UV system. Accordingly, HiBA, acetone, formaldehyde, and formic acid were the primary intermediates of TBA oxidation. The oxidation of acetone in the ozone/UV system generated formaldehyde, pyruvaldehyde, acetic acid, formic acid as primary intermediates. It was also observed that the reaction intermediates formed during the oxidation of TBF react well in the ozone/UV system and complete mineralization could be achieved by the process.