Comparison of different algicides on growth of <Emphasis Type="Italic">Microcystis aeruginosa</Emphasis> and microcystin release,as well as its removal pathway in riverways

Eutrophication with a large number of Microcystis aeruginosa commonly occurs worldwide, thereby threatening the aquatic ecosystem and human health. In this study, four kinds of algicides were tested to explore their influence on cell density and chlorophyll-a of M. aeruginosa. Results showed that aluminum silicate agent, which inhibited more than 90% cell growth compared with the control group, demonstrated the strongest inhibition effect immediately on M. aeruginosa growth. Furthermore, the production and release of microcystin (MC)-LR were investigated. Aluminum silicate, CuSO₄, and Emma-11 were more effective than pyrogallic acid in disrupting the cells of M. aeruginosa, thereby increasing the extracellular MC-LR concentration. Aluminum silicate caused the highest extracellular MC-LR concentration of more than 45 mg·L^–1. Biotoxicity was also detected to evaluate the environmental risks of MC-LR release, which were related to the usages of different algicides. Extracellular MC-LR concentration mostly increased when the biotoxicity of algae solution increased. The experiments were also designed to reveal the effects of physical conditions in riverways, such as natural sunlight, aeration and benthal sludge, on MC-LR degradation. These findings indicated that UV rays in sunlight, which can achieve a MC-LR removal efficiency of more than 15%, played an important role in MC-LR degradation. Among all the physical pathways of MC-LR removal, benthal sludge adsorption presented the optimal efficiency at 20%.

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宁夏电网分区及供电能力研究

针对宁夏电网结构及运行特性发生的变化及日益严重的短路电流超标问题,本文基于宁夏电网“十三五”规划,提出将宁夏电网分为4个区域的供电分区方案。从电力电量平衡、短路电流水平、安全稳定等方面进行分析,并结合短路电流和动态电压稳定裕度指标对分区方案进行最大供电能力研究。结果表明:分区方案合理、有效,可为宁夏“十三五”电网规划提供了技术支持和决策参考。     

京津冀产业碳排放强度变化及驱动因素研究

为探讨京津冀地区温室气体排放强度变化的影响因素,采用对数平均迪式分解模型及归因分析(LMDI-Attribution)方法,基于1996—2014年数据从细分行业角度进行研究。针对温室气体排放强度作产业结构、能源强度和排放因子三因素LMDI乘法分解,对温室气体排放强度变化的影响效应作归因分析,量化4个行业对分解因素影响效应的贡献,得到以下主要结论:1996—2014年京津冀地区温室气体排放强度主要呈现下降趋势,累计下降23.05%。其中,能源强度是温室气体排放强度下降的主导因素,其影响效应为-61.18%,对这一影响效应贡献最大的是工业,并且四大经济部门均通过能源强度在不同程度上使得温室气体排放强度有所减小,可见"阶梯电价"、"千家企业节能项目"、"十大重点节能项目"等相关政策在工业发展中对提高能源效率的作用明显。产业结构使得温室气体排放强度增加23.53%,其主要贡献者是工业,说明"工业产品出口退税率调整"等一系列政策的效果不明显;然而农业则使得温室气体排放强度降低,贡献值为3.09%。碳排放因子在1996—2014年间对温室气体排放强度的影响为60.47%,是京津冀地区温室气体排放强度增加的主要因素,说明京津冀地区的能源结构不合理。工业对这一效应的贡献最大为55.97%。可见,工业在京津冀地区的温室气体减排工作中起到最为关键的作用。     

农户从事生态循环农业意愿与行为的决定:市场收益还是政策激励?

发展生态循环农业是我国新时期转变农业发展方式的战略选择,农户是生态循环农业的经营主体和利益相关者,厘清农户参与生态循环农业的根本动机,对于制定有效的生态循环农业推广措施具有重要意义。文章基于湖北省391份农户调查数据,首先,在文献回顾的基础上提出市场收益、政策激励对农户生态循环农业从事意愿与行为影响路径的基本假设,并利用OLS方法分析市场收益和政策激励对农户从事生态循环农业意愿与行为的影响;其次,运用优势分析法评估市场收益类变量和政策激励类变量影响农户意愿与行为过程中的相对重要性;最后,通过交互效应检验市场收益类变量和政策激励类变量间的交互作用。结果表明:收入预期对农户从事生态循环农业的意愿与行为均有直接的积极影响,是促进农户从事生态循环农业的最重要的因素;焚烧秸秆惩罚政策和废弃物资源化补贴政策对农户从事生态循环农业的意愿有积极影响,沼气池建设补贴政策和废弃物资源化补贴政策对农户生态循环农业行为有促进作用;收入预期与废弃物资源化补贴政策在影响农户生态循环农业行为的过程中存在互补效应。本研究认为,市场收益是刺激农户采纳生态循环农业生产模式的首要因素,因此,要着力完善生态农业市场体系,增强生态农产品的市场竞争力,提升农户对生态循环农业的盈利信心;另外,政策激励对于农户采纳生态循环农业具有促进作用,应该做到约束与激励并行,同时注意加强农业政策的科学设计与落实执行。     

1990~2013年来洞庭湖区鸟类生物多样性热点区时空动态及变动机理

评估与确定生物多样性分布格局与热点区是建立保护区、制定生物保护决策的基础。洞庭湖地区位处长江中游,是我国重要的淡水湖泊湿地生态系统,为中国乃至亚洲较大的鸟类越冬地之一。以洞庭湖地区14种Ⅰ、Ⅱ级重点保护鸟类为指示物种,基于1990~2013年间的多期遥感影像,运用物种生境分布MAXENT模型,选取地形、水系、植被、气候及人类干扰等共35个影响因子,对其进行生境适宜性评价及生物多样性热点区的筛选与制图,并对热点区时空动态特征进行分析。结果表明：（1）鸟类生物多样性热点区的分布范围呈现出组团状特征,1990~2013年来,热点区面积呈下降趋势;（2）鸟类栖息生境景观格局总体上趋于破碎,生境形状向简单且扁平化形态转变,生境格局呈复杂化;（3）经济与社会发展因素对研究区的鸟类生物多样性热点区变化影响显著,而自然因素产生的影响不明显。研究结果在制定区域生物多样性保护规划方案中可体现较好应用价值。     

特朗普“去气候化”政策对全球气候治理的影响

美国特朗普政府宣布退出《巴黎协定》是当前全球气候治理中最受舆论关注的问题,对事态发展趋势的判断和事件影响的评估是最为亟需的。本文系统分析了特朗普政府上任后推行的一系列"去气候化"政策,以及其退出《巴黎协定》的主要动因和可能形式,同时量化评估了这些内政外交的"倒退"对美国实施国家自主贡献目标以及全球气候治理格局的实质影响,并据此提出了中国应对全球气候治理新形势变化的对策和建议。研究表明,特朗普政府"美国优先"的能源政策根植于复兴制造业和加大基础设施投资的经济利益动机,随着特朗普"去气候化"进程持续发酵,诸多气候政策面临存续风险,美国实施国家自主贡献将面临严峻挑战,"倒行政策"将有可能使美国温室气体排放出现反弹。如果不考虑中、高危气候政策,美国2025年温室气体排放也仅能相对2005年下降11.0%—14.9%,距离下降26%—28%的国家自主贡献目标相去甚远。同时,特朗普政府拒绝继续履行向发展中国家提供气候资金支持的义务,将有可能导致绿色气候基金拖欠资金总额上升117%,并进一步挫伤全球低碳投资的信心。没有美国的全球气候治理3.0时代将呈现出新的复杂特征,并不可避免地造成减排、资金和领导力缺口的持续扩大,也不排除后续会出现消极的跟随者,整体进程将可能进入一个低潮周期。虽然国际社会对中国引领全球气候治理充满期待,但中国仍应审慎对待,长远谋划应对气候变化的内政外交战略,而不应将"气候举旗"看作是一蹴而就的短期策略,对各种要求中国发挥"领导作用"的说法保持清醒头脑。在今后气候谈判中,美国仍有较大可能会二次"要价",中国作为排放大国的压力依然不容小觑,中美气候关系需要再定位。     

DO浓度对间歇曝气单级自养脱氮系统N2O排放的影响

以单级自养脱氮系统为研究对象,采用有效容积为15 L的SBBR反应器,系统进水NH+4-N浓度约为360 mg/L,控制温度为(30±2)℃,采用间歇曝气方式运行,曝气段DO浓度从2.4~2.6 mg/L逐渐下降到0.9~1.1 mg/L,研究了单级自养脱氮系统的脱氮性能与N2O排放情况。结果表明,反应器曝气段DO浓度从2.4~2.6 mg/L下降到0.9~1.1mg/L,系统TN去除率均达到80%,但在相同运行时间内的TN去除率依次降低,NH+4-N平均反应速率从0.19 mg/(L·min)降低至0.05 mg/(L·min),NO-3-N累计产生量稳定于14.9~16.5 mg/L,NO-2-N浓度在反应器内未产生明显的积累。随着曝气段DO浓度的下降,最大N2O释放速率逐渐降低,N2O累计释放量从73.8 mg下降到61.0 mg,N2O转化率介于2.4%~2.9%。     

区域水环境系统脆弱性指标体系及综合决策模型研究

目前水环境系统脆弱性研究主要局限于水环境系统的单方面脆弱性研究,过于片面化,需要综合考虑水资源、水环境质量、旱涝灾害、社会经济以及生态环境等方面的脆弱性。根据水环境系统脆弱性是系统状态受到系统压力引起的敏感性以及系统状态对系统压力的适应性响应的观点,采用“压力-状态-响应”模式构建区域水环境系统脆弱性指标体系。区域水环境系统脆弱性研究中客观存在诸多不确定性,利用联系数描述上述不确定性过程中差异度系数在［-1,1］上取值仍存在不确定性,为此,构造三角模糊数刻画差异度系数取值的不确定性,给出三角模糊联系数的基本形式,取置信水平得出置信区间联系数,采用期望-方差排序法对置信区间联系数进行决策分析,建立基于三角模糊联系数的系统综合决策模型。此模型用于安徽省水环境系统脆弱性评价的结果表明,安徽省区域水环境系统脆弱等级介于［2.731 3.620］之间,脆弱性状况不容乐观,应采取相应措施改善区域水环境质量,降低区域水环境系统脆弱性,保障区域社会经济及生态环境的可持续发展     

Environmental effects of soil contamination by shale fuel oils

Estonia is currently one of the leading producers of shale oils in the world. Increased production, transportation and use of shale oils entail risks of environmental contamination. This paper studies the behaviour of two shale fuel oils (SFOs)—‘VKG D’ and ‘VKG sweet’—in different soil matrices under natural climatic conditions. Dynamics of SFOs’ hydrocarbons (C10–C40), 16 PAHs, and a number of soil heterotrophic bacteria in oil-spiked soils was investigated during the long-term (1 year) outdoor experiment. In parallel, toxicity of aqueous leachates of oil-spiked soils to aquatic organisms (crustaceans Daphnia magna and Thamnocephalus platyurus and marine bacteria Vibrio fischeri) and terrestrial plants (Sinapis alba and Hordeum vulgare) was evaluated. Our data showed that in temperate climate conditions, the degradation of SFOs in the oil-contaminated soils was very slow: after 1 year of treatment, the decrease of total hydrocarbons’ content in the soil did not exceed 25 %. In spite of the comparable chemical composition of the two studied SFOs, the VKG sweet posed higher hazard to the environment than the heavier fraction (VKG D) due to its higher mobility in the soil as well as higher toxicity to aquatic and terrestrial species. Our study demonstrated that the correlation between chemical parameters (such as total hydrocarbons or total PAHs) widely used for the evaluation of the soil pollution levels and corresponding toxicity to aquatic and terrestrial organisms was weak.     

Behavior and mechanism of arsenate adsorption on activated natural siderite: evidences from FTIR and XANES analysis

Activated natural siderite (ANS) was used to investigate its characteristics and mechanisms of As(V) adsorption from aqueous solution. Batch tests were carried out to determine effects of contact time, initial As(V) concentration, temperature, pH, background electrolyte, and coexisting anions on As(V) adsorption. Arsenic(V) adsorption on ANS well-fitted pseudo-second-order kinetics. ANS showed a high-adsorption capacity of 2.19 mg/g estimated from Langmuir isotherm at 25 °C. Thermodynamic studies indicated that As(V) adsorption on ANS was spontaneous, favorable, and endothermic. ANS adsorbed As(V) efficiently in a relatively wide pH range between 2.0 and 10.0, although the removal efficiency was slightly higher in acidic conditions than that in basic conditions. Effects of background electrolyte and coexisting anions were not significant within the concentration ranges observed in high As groundwater. Results of XRD and Fe K-edge XANES analysis suggested ANS acted as an Fe(II)/(III) hybrid system, which was quite effective in adsorbing As from aqueous solution. There was no As redox transformation during adsorption, although Fe(II) oxidation occurred in the system. Two infrared bands at 787 and 872 cm^?1 after As(V) adsorption suggested that As(V) should be predominantly adsorbed on ANS via inner-sphere bidendate binuclear surface complexes.