不同离子对黑土胶体在土壤中运移的影响

黑土样品采自于黑龙江海伦市,提取胶体并对其主要理化性质进行定性定量表征,通过淋滤实验研究胶体在土柱中的运移特征以及不同离子及其强度对胶体运移的影响。结果显示:所提取胶体粒径与理论计算基本吻合,粒径主要分布在2~5μm;当pH由4上升到9时,胶体的zeta电位则由-26.43mV降低到-34.52mV;红外光谱显示胶体颗粒的有机机团主要为-OH、CH-、C=O、多糖;X射线衍射表明其主要矿物组成是石英(56.9%)。不同离子及其强度对胶体的在土壤中的运移有较为明显的影响,当pH由4增加到9时,k值由6.020×10-4降低至3.858×10-4,Ca2+、K+、Na+当离子强度由0.5mmol/L变化到0.001mmol/L时,k值分别由6.087×10-4降低至4.024×10-4、5.518×10-4降低至3.818×10-4、5.401×10-4降低至4.109×10-4。     

地下水中污染物的迁移传输及排泄通量研究

以辽宁某化工污染场地为研究对象,结合场地调查结果,应用地下水模型系统软件(GMS)中的MODFLOW和RT3D模型,建立了地下水中污染物的数值模型,探讨其迁移传输及排泄通量。根据模拟结果,地下水中苯、二氯苯和三氯苯的污染羽约在20年后达到动态平衡,污染羽不再随时间变化,污染物的自然衰减速率与污染源释放速率达到平衡。排泄通量估算表明:地下水向河流排泄的量在20年时达到稳定,地下水中苯、二氯苯和三氯苯向河流的排泄通量分别为每天180 g、6 100 g和5.5 g。由于污染物会导致污染生态环境和健康风险,建议从控制污染源、实施污染源区修复和切断迁移传输途径等多种措施控制风险。     

机动车排气检验机构的环境影响评价研究

机动车排气定期检验机构对周边环境质量的影响虽然不大,但由于大多处在闹市区,贴近敏感人群,其噪声与机动车尾气对市民的影响却不容忽视。通过环境影响评价,分析机动车排气定期检验机构的环境影响特点,并结合机动车排气定期检验业务流程,对机动车排气定期检验机构的整体规划与布局提出合理建议,对噪声与大气污染物排放提出有效控制措施,不仅可以有效控制机动车排气定期检验机构对周边大气环境质量的影响,也能有效减小噪声对周边市民日常生活的影响。     

中国地区二次有机气溶胶的时空分布特征和来源分析

二次有机气溶胶(SOA)由于其在大气污染、气候变化与人体健康方面的影响,是我国大气环境中一种重要的污染物.确定中国SOA分布规律以及产生来源是大气污染防治的前提.利用全球化学传输模型(Model for Ozone and Related Chemical Tracers,Version 4,MOZART4)并集成多相SOA参数化方案,模拟了中国地区SOA的时空分布,并按前体物分区域进行了来源分析.结果表明,受SOA前体物排放分布的影响,中国地区的SOA主要分布在东部和南部地区,并且夏季SOA产量是冬季产量的2.5倍.中国地区分布的SOA由人为源排放产生占55%,高于自然源(45%);并且境内排放贡献了我国SOA产量的77%,主要影响东部近地面大气的浓度分布.境外排放主要影响我国西部地区,尤其是对高空SOA分布影响显著.     

基于城市功能区划分的道路机动车大气污染物排放清单研究——以厦门市海沧区为例

道路机动车尾气排放是造成城市近地面空气污染的主要原因之一,建立基于城市功能区划分的道路机动车大气污染物排放清单对改善中观尺度的城市空气质量具有重要辅助作用.本文以厦门市海沧区为例,基于城市功能区划分方法,结合各功能区内监测道路的机动车通行量实测数据,建立道路机动车大气污染物排放清单,并分析各功能区道路机动车大气污染物排放特征.结果发现,海沧区道路机动车尾气排放物中CO的排放贡献率最高,工业区和居住区的道路机动车大气污染物排放量对海沧区的空气污染贡献率最大,海沧区夜间大气污染物的主要排放源来自于工业区道路机动车大气污染物排放;生态服务区及公共管理与公共服务区的道路机动车排放特征受相邻工业区机动车大气污染物排放的影响较为显著.研究表明:城市功能区分布欠合理是导致道路机动车大气污染物高排放量的重要原因之一;基于城市功能区划分构建道路机动车大气污染物排放清单的研究方法,不仅可为中观尺度下的城市大气污染排放情况提供有效的调查途径,而且能为城市功能格局的合理规划提供重要的理论依据.     

应用WRF/Chem模拟河南冬季大气颗粒物的区域输送特征

基于WRF/Chem模式,设置多组区域排放源的情景实验定量估算河南、京津冀、山东、山西、安徽和江苏、湖北6个区域人为源排放对河南省2015年12月PM_(2.5)和PM_(10)浓度贡献率,并结合气象资料研究3个代表性城市的污染输送特征.结果表明:河南省冬季PM_(2.5)和PM_(10)主要来源为本省排放,平均贡献率分别为54.83%、61.32%.区域污染输送对河南颗粒物的贡献也占有很大比例,京津冀、安徽和江苏、山东、山西以及湖北对PM_(2.5)平均贡献率分别为11.95%、11.69%、7.95%、7.40%、4.30%,对PM_(10)平均贡献率分别为10.42%、10.03%、7.00%、6.89%、3.80%.PM_(2.5)外来输送率比PM_(10)要高,表明细颗粒物比粗颗粒物更易跨区域长距离输送.冬季长持续时间的污染过程大多受静风或小风控制,省内污染贡献最大,过程结束时伴随着大风,周边区域的污染贡献有所增加.不同城市的颗粒物来源与其地理位置、风速、风向等气象条件密切相关.区域污染来源具有复杂性,改善河南省空气质量是需要整个区域共同面对和解决的问题.     

不同季节气象条件对北京城区高黑碳浓度变化的影响

利用2013年至2015年北京城区黑碳气溶胶(下文统称为"BC")和PM2.5观测资料,结合地面气象观测资料、ECMWF边界层高度再分析资料和FNL/NCEP不同高度风速再分析资料,讨论了BC质量浓度及其在PM_(2.5)质量浓度中所占比例(下文统称"黑碳占比")的季节、月、日变化特征,并通过计算北京城区BC浓度与不同高度风速的相关矢量,分析了气象条件和外来输送对北京城区BC浓度变化的影响.结果发现:研究时段内北京城区BC浓度平均值为(4.77±4.49)μg·m~(-3);黑碳占比为8.23%±5.47%.BC浓度和黑碳占比在春、夏季低,秋、冬季高,其日变化特征在4个季节均为"白天低夜间高"的单峰型特征.随着PM_(2.5)浓度的升高,BC浓度增大,黑碳占比减小.当北京地区风向为东北、东北偏东、东南和西南偏西(主风向)时,BC浓度与风速和边界层高度均呈反向变化,即随风速和边界层高度的增大而减小.另外不同季节BC浓度随风速变化的临界值及其变化速率不同.冬季高BC浓度时段,北京城区BC浓度在低层大气的关键影响区分别位于河北南部与山东交界地区以及河北西北部与山西内蒙交界地区;高空关键影响区主要位于北京以西的河北西部、山西北部和内蒙古地区.     

大宝山矿区水体中重金属的行为研究

广东大宝山矿区矿山废水的排放使周边生态环境遭受了严重的破坏。水体中重金属Cu、Zn、Cd和Pb的溶解态浓度分别达到13.82、50.83、0.103和2.91 mg.L-1。Cu、Zn、Cd和Pb的溶解态和悬浮态含量沿河流主干道断面呈相似的空间分布规律,上游都是沿水流方向降低,下游因吸附于悬浮物中的重金属重新释放略有增加。悬浮物中重金属元素的化学形态提取和扫描电镜能谱分析(SEM/EDAX)表明:4种重金属元素都以残渣态为主要存在形态,其次为可还原态,个别断面的Cd可还原态甚至超过了残渣态的含量,说明该水体这4种元素对环境都有一定的潜在威胁性。     

Modification of the biochemical pathways of plants induced by ozone: what are the varied routes to change?

When plants are observed under a low dose of ozone, some physiological and metabolic shifts occur. Barring extreme injury such as tissue damage or stomata closure, most of these disruptive changes are likely to have been initiated at the level of gene expression. The belief is oxidative products formed in ozone exposed leaves, e.g. hydrogen peroxide, are responsible for much of the biochemical adjustments. The first line of defense is a range of antioxidants, such as ascorbate and glutathione, but if this defense is overwhelmed, subsequent actions occur, similar to systemic acquired resistance or general wounding. Yet there are seemingly unrelated metabolic responses which are also triggered, such as early senescence. We discuss here the current understanding of gene control and signal transduction/control in order to increase our comprehension of how ozone alters the basic metabolism of plants and how plants counteract or cope with ozone.     

Dioxins,chlorophenols and other chlorinated organic pollutants in colloidal and water fractions of groundwater from a contaminated sawmill site

BACKGROUND, AIM, AND SCOPE: The distribution of chlorinated organic contaminants in groundwater and the importance of colloids were studied in groundwater from a sawmill site contaminated by chlorophenol preservatives. MATERIALS AND METHODS: The groundwater was fractionated into three different size ranges: (1) >0.7 mum, (2) 0.4-0.7 mum and (3) 0.2-0.4 mum and the filtered water phase. The concentrations of chlorophenols (CP), chlorinated phenoxy phenols (PCPP), chlorinated diphenyl ethers (PCDE), chlorinated dibenzofurans (PCDF) and chlorinated dibenzo-p-dioxins (PCDD) were determined in each fraction. The colloids were characterised regarding the chemical composition using X-ray photoelectron spectroscopy (XPS). RESULTS: Chlorophenols were mostly found in the water fraction and PCDD/Fs were found almost exclusively in the particulate fractions. For example, the filtered water phase contained 2,100 mug l(-1) and 0.72 ng l(-1) for CPs and PCDD/Fs, respectively, and the particulate fractions contained 27 mug l(-1) and 32 ng l(-1) for CPs and PCDD/Fs, respectively. XPS evaluation of the particulate phases showed no correlation between the surface chemistry of the particle properties and the distribution of chlorinated compounds. DISCUSSION: The results suggest that groundwater transport of CPs, PCPPs, PCDEs and PCDD/Fs may occur from contaminated sawmill sites and that the colloid-facilitated transport, especially of PCDD/Fs, is substantial. The results correlated well with previous studies of compounds sorbed to dissolved organic carbon, which indicate that dissolved and colloidal organic carbon facilitated the transport of PCDEs, PCDFs and PCDDs particularly. CONCLUSIONS: Several classes of chlorinated compounds were readily detected in the groundwater samples. Due to the differences in their physicochemical properties, CPs, PCPPs, PCDEs and PCDD/Fs vary in their partitioning between colloidal fractions and the filtered groundwater. The proportion of the bound fraction increased with an increasing hydrophobicity of the chlorinated compounds. The groundwater transport of colloid-associated pollutants from the site may be significant. RECOMMENDATIONS AND PERSPECTIVES: The results imply that colloidal particles <0.7 mum are freely mobile in groundwater from this site. The groundwater transport of colloid-associated pollutants may be significant. However, the extent of the problem is not yet known and, thus, further research is needed to evaluate the impact of colloidal transport of hydrophobic organic contaminants. In Sweden alone, 400 to 500 sawmill sites are estimated to be contaminated with PCDD/Fs as a result of the former use of CP-based wood preservatives. The widespread use of CP mixtures for a variety of applications, including wood preservation, indicates that potential colloidal transport will be an issue of concern in many countries.