田间施用锌肥对小麦籽粒镉累积的影响及施用风险

锌（Zn）和镉（Cd）的交互作用是近年来小麦Cd污染防治的重要研究方向.以华北地区典型小麦田为研究对象,通过田间试验,探究Zn肥对土壤-小麦系统Cd污染的控制效果和施用风险.结果表明,低用量Zn处理下,济源和开封两地小麦籽粒Cd含量均呈下降趋势,与对照相比下降幅度分别为33.4%和25.3%.高用量Zn处理下,两地小麦籽粒Cd含量不降反升,与低用量Zn处理下小麦籽粒Cd含量相比增幅为22.4%和34.2%.施Zn后两地土壤Zn总量和有效态含量均有显著升高,且造成了土壤Cd的部分活化.典型相关分析（CCA）显示,当土壤ω（Zn）小于200 mg ·kg^-1时,土壤Zn是土壤-小麦系统Cd富集的主要影响因子,而当土壤ω（Zn）大于200 mg ·kg^-1时,土壤Cd的活化是影响小麦籽粒Cd富集的主要原因.回归分析显示土壤Cd/Zn降至0.0089时（低用量Zn）,Zn和Cd表现出拮抗效应,土壤Cd/Zn降至0.0078时（高用量Zn）,Zn和Cd表现出协同效应.针对区域Cd污染特征,调整Zn肥用量可以提高污染防治效率并避免加剧Cd污染危害.     

宣城向阳剖面网纹红土粒度端元分析及指示意义

对宣城向阳剖面的109个网纹红土样本做粒度分析和地球化学元素分析,并对粒度数据采用合适的端元分解方法,将各端元与地球化学指标在深度上进行了对比。结果认为:端元法可以把代表此区域3种不同动力的沉积端元(EM)分离出来,并可以定量地分析各自所占比重及各个阶段每种动力各自的沉积变化。EM1明显指示着对原有沉积物的成壤改造作用;EM2可能代表着东亚冬季风作用下经远距离悬浮搬运并在湿润的宣城地区沉积而受到化学风化影响的组分;EM3则比较明显地代表着受东亚夏季风作用下的化学风化及近源搬运作用。各端元在深度上的变化过程一定程度上揭示了区域气候背景的变化信息,为更进一步的气候变化研究及网纹红土中网纹成因研究提供了一种新的思路。     

扎龙湿地丹顶鹤繁殖栖息地的选择及扩散

景观演变对野生动物栖息地质量和连接度造成的影响,一直是威胁全球生物多样性保护的关键问题,开展扎龙湿地丹顶鹤（Grus japonensis）繁殖栖息地选择及繁殖期生境间的扩散研究,对野生丹顶鹤的保护具有重要的意义。首先利用需要“出现点”的生态位MAXENT模型,进行适宜栖息地选择研究。从水源、食物、干扰、隐蔽物四个方面选择明水面距离、土壤湿度、NDVI、道路距离和居民地距离五个环境变量作为丹顶鹤繁殖栖息地选择的影响因子,预测扎龙保护区可供丹顶鹤进行营巢繁殖的栖息地分布,并分析各影响因子的反应曲线。结果显示：丹顶鹤易于选择远离道路和居民地干扰且靠近明水面的区域作为营巢栖息地,栖息地土壤湿度较高并且植被覆盖较多。从MAXENT模型中提取了38个适宜栖息地斑块,基于电路理论模拟丹顶鹤繁殖期失去飞行能力时的多路径扩散,最大电流密度图突出了可能的“夹点”,模拟出具有一定宽度范围的连接区域,可供丹顶鹤在繁殖期间进行扩散。累积电流密度图突出了在维持网络连通性方面起到积极作用的斑块,并进行面积加权来评估适宜栖息地斑块的综合重要性。结果表明,在MAXENT模型预测出的适宜栖息地斑块基础上,考虑丹顶鹤繁殖期的迁移扩散行为,利用累积电流密度面积加权来评估适宜栖息地斑块的综合重要性,得到的适宜性等级更符合丹顶鹤真实巢址的分布。研究成果可为保护区丹顶鹤栖息繁殖生境的恢复和保护提供科学依据。     

基于生态安全格局与生态脆弱性评价的生态修复关键区域识别与诊断——以汶上县为例

以山东省济宁市汶上县为研究区,基于最小阻力模型构建生态安全格局,结合脆弱性评价识别生态修复关键区域,对关键区域分类提出针对性修复保护措施.结果表明在汶上县共识别出11处生态源地,总面积38.72km²,35条生态廊道,总长度259.56km;生态脆弱性分级以中度脆弱与低度脆弱为主,两类型区域总面积594.32km²,占比67.40%.中部城区脆弱性较高,西南洼地脆弱性较低;识别出生态修复关键区域5处,总面积107.14km²,分布于中部城区及周边;根据区位特征将关键区域分为三类,并分类别提出其生态修复策略,以期为国土空间生态修复提供参考.     

Effect of photo-biodegradation and biodegradation on the biogeochemical cycling of dissolved organic matter across diverse surface water bodies

The objective of this research was to quantify the temporal variation of dissolved organic matter(DOM) in five distinct waterbodies in watersheds with diverse types of land use and land cover in the presence and absence of sunlight. The water bodies were an agricultural pond, a lake in a forested watershed, a man-made reservoir, an estuary, and a bay. Two sets of samples were prepared by dispensing unfiltered samples into filtered samples in 1:10 ratio(V/V). The first set was exposed to sunlight(10 hr per day for 30 days) for examining the combined effect of photo-biodegradation, while the second set was stored in dark for examining biodegradation alone. Spectroscopic measurements in tandem with multivariate statistics were used to interpret DOM lability and composition. The results suggest that the agricultural pond behaved differently compared to other study locations during degradation experiments due to the presence of higher amount of microbial humic-like and protein-like components derived from microbial/anthropogenic sources. For all samples, a larger decrease in dissolved organic carbon(DOC) concentration(10.12% ±9.81% for photo-biodegradation and 6.65% ± 2.83% for biodegradation) and rapid transformation of DOM components(i.e., terrestrial humic-like components into microbial humic and protein-like components) were observed during photo-biodegradation experiments.Results suggest that sunlight facilitated DOM biodegradation, resulting in simpler recalcitrant molecules regardless of original composition. Overall, it was found that combined effects of light and bacteria are more efficient than bacterial effects alone in remineralizing and altering DOM, which highlights the crucial importance of sunlight in transforming aquatic DOM.     

PM2.5-bound polycyclic aromatic hydrocarbons (PAHs) in Beijing: Seasonal variations, sources, and risk assessment

Polycyclic aromatic hydrocarbons(PAHs) have been of health concern due to its carcinogenesis and mutagenesis. In this study, we aimed to assess the variations, sources, and lifetime excessive cancer risk(ECR) attributable to PAHs bound to ambient particulate matters with aerodynamic diameter less than 2.5 μm(PM_(2.5)) in metropolitan Beijing, China. We collected24-hour integrated PM_(2.5) samples on daily basis between November 2014 and June 2015 across both central heating(cold months) and non-heating(warm months) seasons, and further analyzed the PAH components in these daily PM_(2.5) samples. Our results showed that total concentrations of PM_(2.5)-bound PAHs varied between(88.6 ± 75.4) ng/m~3 in the cold months and(11.0 ± 5.9) ng/m~3 in the warm months. Benzo[a]pyrene(Ba P), the carcinogenic marker of PAHs,averaged at 5.7 and 0.4 ng/m~3 in the cold and warm months, respectively. Source apportionment analyses illustrated that gasoline, biomass burning, diesel, coal combustion and cooking were the major contributors, accounting for 12.9%, 17.8%, 24.7%, 24.3% and 6.4% of PM_(2.5)-bound PAHs, respectively. The BaP equivalent lifetime ECR from inhalation of PM_(2.5)-bound PAHs was 16.2 cases per million habitants. Our results suggested that ambient particulate reduction from energy reconstruction and adaption of clean fuels would result in reductions PM_(2.5)-bound PAHs and its associated cancer risks. However, as only particulate phased PAHs was analyzed in the present study, the concentration of ambient PAHs could be underestimated.     

Physicochemical analysis of individual atmospheric fine particles based on effective surface-enhanced Raman spectroscopy

Fine particles associated with haze pollution threaten the health of more than 400 million people in China. It is therefore of great importance to thoroughly investigate and understand their composition. To determine the physicochemical properties in atmospheric fine particles at the micrometer level, we described a sensitive and feasible surface-enhanced Raman scattering(SERS) method using Ag foil as a substrate. This novel method enhanced the Raman signal intensities up to 10,000 a.u. for ν(NO_3~-) in fine particles.The SERS effect of Ag foil was further studied experimentally and theoretically and found to have an enhancement factor of the order of ～10~4. Size-fractionated real particle samples with aerodynamic diameters of 0.4–2.5 μm were successfully collected on a heavy haze day,allowing ready observation of morphology and identification of chemical components, such as soot, nitrates, and sulfates. These results suggest that the Ag-foil-based SERS technique can be effectively used to determine the microscopic characteristics of individual fine particles, which will help to understand haze formation mechanisms and formulate governance policies.     

完全混合式曝气系统运行特性及微生物群落结构解析

利用某污水处理厂完全混合式曝气系统处理生活污水,探讨了系统同步硝化反硝化脱氮过程,解析了系统中污泥微生物群落结构.中试试验结果表明,系统运行稳定,且在无外加碳源的条件下,COD、氨氮和总氮平均去除率分别为93.2%、96.9%和75.2%,出水COD、氨氮和总氮均优于一级A排放标准.系统污泥具有较强的反硝化能力,其脱氮速率是污水处理厂污泥的2.86倍以上.通过对系统污泥周质硝酸盐还原酶聚合酶链式反应(polymerase chain reaction,PCR)扩增和高通量测序结果,发现系统中存在好氧反硝化菌,污泥中优势菌为动胶菌属(Zoogloea)、陶厄氏菌属(Thauera)和Dechloromonas菌属.     

天然/模拟海水中2,4,6-三溴苯酚的光化学行为研究

有机溴代苯酚类污染物在水体中普遍存在,尤其在海洋环境中,除人为污染源外,它还存在广泛的天然来源.以2,4,6-三溴苯酚为模型化合物,以氙灯(λ290 nm)作为模拟太阳光源,研究了海水中溴代苯酚的光化学过程,并系统考察了溴代苯酚初始浓度、Cl~-、Fe(Ⅲ)和pH值等环境因素的影响.实验结果表明,在海水中,2,4,6-三溴苯酚能够快速发生光化学反应,通过产物分析发现其主要产物为通过光致脱溴氯代过程产生的2,4-二溴-6-氯苯酚,并且该产物随2,4,6-三溴苯酚初始浓度、Cl~-浓度、Fe(Ⅲ)浓度的增大及溶液pH值的降低而增加.以明亮发光杆菌为受试生物的毒理学实验表明,2,4,6-三溴苯酚在海水中光化学的前期,系统的毒性效应增强,而毒性的增加可能主要由光致氯代过程导致.     

再生水中色度物质的识别及其臭氧去除特性

针对我国再生水普遍存在的色度问题,以天津市某污水厂二级出水为研究对象,采用三维荧光光谱和GC/MS技术对其进行组成分析,结果表明:再生水中主要带色物质为富里酸与腐殖酸类物质,同时还存在偶氮二甲酸二乙酯、N,N-二甲基乙醇胺、苄醚、1,4-二甲基吡啶氯化物等导致再生水色度的带色有机物。在再生水的臭氧降解实验中,臭氧可有效降解再生水中的富里酸与腐植酸类物质,去除率分别达到96.5%、97.3%。臭氧对再生水的色度与CDOM(有色溶解有机物)的降解也表现出了良好的效果,2 min内去除率可分别达到93.1%、86.2%。并且在色度物质的臭氧降解过程中,臭氧的直接反应占据主导地位,而并非与·OH的间接反应。该结果对再生水臭氧氧化工艺的设计应用有现实的指导意义。