凤阳山森林生态系统碳交换及其物候特征

凤阳山位于浙江省龙泉市南部,为亚热带典型森林生态系统保护区,受海洋性气候和季风的影响,是研究森林生态系统碳预算及其物候特征的理想之地。采用位于浙江凤阳山的涡动相关通量观测系统（EC）观测的2017年（除去9月）CO₂通量数据、气象数据并结合物候模型来分析本地尺度亚热带森林生态系统总初级生产力（GPP）、生态系统呼吸（Re）动态特征、不同时间尺度下的影响因子及其物候特征,结果表明：该生态系统全年扮演着碳汇的角色,净生态系统碳交换量（NEE）（除去9月）为?89 g?m^?2?a^?1（以碳计）,GPP总量为1377.75 g?m^?2?a^?1,Re总量为1288 g?m^?2?a^?1,GPP和Re的日变化和季节变化均呈单峰型,先增加后降低。GPP在不同的物候时期均为倒“U”型的变化趋势,而Re在夜间的生态系统呼吸略高于白天,且在日夜交替时刻会出现陡降现象。整个生态系统在174 d GPP增长率达到峰值0.25 μmol?m^?2?s^?1,达到最大恢复率;202 d的GPP增长率为0 μmol?m^?2?s^?1;228 d的GPP增长率最低,为?0.21 μmol?m^?2?s^?1,达到最大衰退率。不论是日尺度还是月尺度上,GPP和Re变化的主要驱动因素为空气温度,日尺度上Re较GPP对环境因子的变化更加敏感;反之,在月尺度上GPP对环境因子变化的响应比Re更加敏感。总体而言,凤阳山森林生态系统全年表现为碳汇,能够调节当地的二氧化碳浓度;生长季森林生态系统生长旺盛,稳定阶段的GPP与Re达到峰值;在不同的时间跨度上生态系统对环境因子的响应存在差异。     

成都市PM2.5中无机组分与硝酸盐氮氧同位素变化特征

2013年1月12日～2013年1月23日和2014年8月10日～2014年8月21日在成都市城东成都理工大学校园内按昼夜采集PM_(2.5)样品,分析了PM_(2.5)样品的质量浓度、9种水溶性无机离子含量和硝酸盐的δ~(15)N和δ~(18)O。结果表明,采样期间成都市PM_(2.5)冬、夏季的质量浓度分别为161～677μg/m~3(360±118μg/m~3)和87～137μg/m~3(92±18μg/m~3),冬季超标2～9倍,属于重度污染,夏季超标1～2倍,属于轻度污染; SO_4~(2-)、NO_3~-和NH_4~+(SNA)的质量浓度占总水溶性无机离子和PM_(2.5)质量浓度的比值冬夏季分别为72%±14. 3%和65%±9. 2%,21. 1%±2. 5%和30. 3%±6. 9%,是主要的无机离子组分。结合离子相关性分析,SNA的存在形式在白天以(NH_4)_2SO_4或NH_4HSO_4为主,部分以NH_4NO_3的形式存在,而在夜间则以NH_4NO_3为主,部分以(NH_4)_2SO_4或NH_4HSO_4形式存在。成都市PM_(2.5)中硝酸盐的δ~(15)N和δ~(18)O呈冬季高、夏季低的特征。冬季,硝酸盐来源于燃煤和机动车尾气;夏季,硝酸盐来源于机动车尾气、燃煤和农业土壤释放,根据其[NO_3~-]/[SO_4~(2-)]值说明成都市冬夏季均以固定污染源(燃煤)为主,移动污染源(机动车尾气)为辅。成都市冬季大气颗粒物中硝酸盐主要由NO_x经O_3氧化形成,夏季主要经·OH氧化形成硝酸盐或N_2O_5水解生成硝酸盐。     

黄河下游开封段引黄灌区小麦中重金属污染特征及健康风险评价

为探究引黄灌区小麦对人体健康的影响,以黄河下游引黄灌区开封段为研究区,对其中水稻乡、柳园口乡、西郊乡和北郊乡的小麦进行采样调查,采用内梅罗综合指数法、健康风险评价模型对研究区小麦重金属污染状况及其对成人和儿童的健康风险进行评价.结果表明,研究区小麦籽粒中Cd、Cr、Pb、Cu、Zn、Ni、Hg平均含量分别为0.034、0.428、0.279、5.363、29.605、0.305和0.003 mg·kg~(-1).除Pb和Zn外,其他重金属均未超出国家食品卫生标准限制值.研究区小麦籽粒中Pb和Zn的污染指数大于1,Cd、Cr、Cu、Ni和Hg的污染指数均小于1,小麦综合污染指数为1.9851,各乡区小麦的综合污染指数介于1.116~1.847之间.非致癌重金属(Pb、Cu、Zn、Hg)对成人和儿童的健康风险指数分别为1.055 8和0.545 0;致癌重金属(Cd、Cr、Ni)对成人和儿童的健康风险指数均值均高于USEPA推荐的最大可接受风险水平1×10-4,可能存在引发癌症的风险.     

Performance and fouling mechanism of direct contact membrane distillation (DCMD) treating fermentation wastewater with high organic concentrations

In this study,direct contact membrane distillation(DCMD)was used for treating fermentation wastewater with high organic concentrations.DCMD performance characteristics including permeate flux,permeate water quality as well as membrane fouling were investigated systematically.Experimental results showed that,after 12 hr DCMD,the feed wastewater was concentrated by about a factor of 3.7 on a volumetric basis,with the permeate flux decreasing from the initial 8.7 L/m~2/hr to the final 4.3 L/m~2/hr due to membrane fouling;the protein concentration in the feed wastewater was increased by about 3.5 times and achieved a value of 6178 mg/L,which is suitable for reutilization.Although COD and TOC in permeate water increased continuously due to the transfer of volatile components from wastewater,organic rejection of over 95%was achieved in wastewater.GC–MS results suggested that the fermentation wastewater contained 128kinds of organics,in which 14 organics dominated.After 12 hr DCMD,not only volatile organics including trimethyl pyrazine,2-acetyl pyrrole,phenethyl alcohol and phenylacetic acid,but also non-volatile dibutyl phthalate was detected in permeate water due to membrane wetting.FT-IR and SEM–EDS results indicated that the deposits formed on the membrane inner surface mainly consisted of Ca,Mg,and amine,carboxylic acid and aromatic groups.The fouled membrane could be recovered,as most of the deposits could be removed using a HCl/Na OH chemical cleaning method.     

外部性视角下的节水灌溉技术补偿标准核算——基于选择实验法

合理的补偿标准是节水灌溉技术补偿政策的核心,也是促进农户技术采用的关键内容。论文以石羊河下游民勤县为例,通过选择实验调研和RPL（Random Parameters Logit）模型估计,量化了节水灌溉技术采用的外部效益,并结合特定技术与农户谈判能力讨论了兼顾公平与效率的补偿标准。结果表明：民勤县城乡居民均希望实施节水灌溉技术来改善生态环境,技术采用的外部效益约为1 052.25元/hm²;以膜下滴灌技术为例,合理的补偿标准应在789.15元/hm²左右。从现行政策看,过低的补贴标准难以保障农户切身利益,导致政策响应不足。据此建议,完善成本收益核算体系,将技术采用的外部效益纳入补偿标准的核算中,提升补偿政策的公平性,同时也要根据技术类型及其采用面积进行精准化补偿,保障资金有效利用。     

Observation and analysis of atmospheric volatile organic compounds in a typical petrochemical area in Yangtze River Delta, China

Volatile organic compounds (VOCs) are a kind of important precursors for ozone photochemical formation. In this study, VOCs were measured from November 5th, 2013 to January 6th, 2014 at the Second Jinshan Industrial Area, Shanghai, China. The results showed that the measured VOCs were dominated by alkanes (41.8%), followed by aromatics (20.1%), alkenes (17.9%), and halo-hydrocarbons (12.5%). The daily trend of the VOC concentration showed a bimodal feature due to the rush-hour traffic in the morning and at nightfall. Based on the VOC concentration, a receptor model of Positive Matrix Factorization (PMF) coupled with the information related to VOC sources was applied to identify the major VOC emissions. The result showed five major VOC sources: solvent use and industrial processes were responsible for about 30% of the ambient VOCs, followed by rubber chemical industrial emissions (23%), refinery and petrochemical industrial emissions (21%), fuel evaporations (13%) and vehicular emissions (13%). The contribution of generalized industrial emissions was about 74% and significantly higher than that made by vehicle exhaust. Using a propylene-equivalent method, alkenes displayed the highest concentration, followed by aromatics and alkanes. Based on a maximum incremental reactivity (MIR) method, the average hourly ozone formation potential (OFP) of VOCs is 220.49?ppbv. The most significant source for ozone chemical formation was identified to be rubber chemical industrial emissions, following one by vehicular emission. The data shown herein may provide useful information to develop effective VOC pollution control strategies in industrialized area.     

中国东海至南大洋航线海洋近地层大气NOx分布特征

为了探究我国东海至南大洋航线海洋近地层大气NO_x的分布特征,于2015年11月-2016年1月,利用中国极地科学考察船"雪龙号"的观测平台,采用Saltzman法对中国东海至南大洋航线海洋近地层大气NO_x日均浓度进行了监测.结果表明,中国东海至南大洋航线海洋近地层大气ρ（NO_x）的变化范围为0.001~0.038 mg/m3,ρ（NO）的变化范围为0.001~0.033 mg/m3,ρ（NO₂）的变化范围为0（未检出）~0.015 mg/m3.中国东海至南大洋航线海洋近地层大气中,NO是NO_x的主要成分.南极圈外海洋近地层大气中NO_x的分布特征显示距离陆地越近,ρ（NO_x）越高,NO₂/NO（二者质量浓度比值）越大,反映出海陆差异及人为污染对海洋近地层大气的影响.远离陆地的南大洋航段ρ（NO_x）显示较低的大洋背景值.南桑威奇群岛的火山活动导致附近海域异常高浓度的NO_x分布,ρ（NO_x）最高值达0.160 mg/m3,ρ（NO）为0.145 mg/m3,ρ（NO₂）为0.015 mg/m3.西风带的阻隔导致该区域NO_x向周围扩散时,难以穿越西风带,向南极大陆边缘扩散的趋势更加强烈,影响大范围南大洋近地层大气NO_x分布.人为活动可能是南极半岛和中山站附近海洋近地层大气高ρ（NO_x）和高NO₂/NO的原因之一.      

Energy-saving benefits from plug-in hybrid electric vehicles: perspectives based on real-world measurements

Promoting plug-in hybrid vehicles (PHEV) is one important option to mitigate greenhouse gas emissions and air pollutants for road transportation sector. In 2015, more than 220,000 new PHEVs were registered across the world, indicating a 25-fold growth during 2011–2015. However, more criticizes have been put forward against the current energy efficiency regulations for vehicles that are mostly depended on laboratory measurements. To better understand the real-world energy-saving and emission mitigation benefits from PHEVs, we conducted on-road testing experiments under various operating conditions for two in-use PHEVs in Beijing, China. Our results indicate that air condition usage, congested traffic conditions, and higher loading mass could significantly increase energy consumption and shorten actual all-electric distance for PHEVs. For example, the worst case (14.1 km) would occur under harshest usage conditions, which is lower by at least 35% than the claimed range over 20 km. In charge sustaining (CS) mode, real-world fuel consumption also presents a large range from 3.5 L/100 km to 6.3 L/100 km because of varying usage conditions. Furthermore, various vehicle users have significantly different travel profiles, which would lead to large heterogeneity of emission mitigation benefits among individual PHEV adopters. Therefore, this study suggests that the global policy makers should use real-world energy efficiency of emerging electrified powertrain techniques as criteria to formulate relevant regulations and supportive policies.     

Co(Ⅱ)活化过氧乙酸降解有机染料研究

采用Co(Ⅱ)活化过氧乙酸(PAA)降解有机染料,主要评估了Co(Ⅱ)/PAA体系的氧化性能并考察不同因素对酸性橙(AO7)脱色的影响.结果表明:Co(Ⅱ)/PAA体系能有效脱色有机染料,其氧化能力与Co(Ⅱ)/PMS体系相当并优于Fenton体系. AO7的脱色效果随PAA和Co(Ⅱ)浓度的升高而升高,其中,[Co(Ⅱ)]_0为0.01 mmol·L~(-1)、[PAA]_0/[AO7]_0为4/1时,反应60 min可使92%的AO7脱色.弱酸或中性的环境有利于AO7的脱色,存在Cl-和HA时不利于AO7的脱色.采用抑制剂抗坏血酸、叔丁醇、甲醇等实验方法,推测Co(Ⅱ)/PAA体系中产生的CH_3COO·和CH_3COOO·是对AO7起主要降解作用的自由基.紫外可见光谱分析表明,该自由基主要攻击AO7分子中的偶氮键及萘环结构,从而达到AO7脱色效果.     

表面活性剂复配修饰添加不同含量蒙脱石的黄棕壤对苯酚的吸附作用

在两性修饰剂十二烷基二甲基甜菜碱(BS-12)和阳离子型表面修饰剂十六烷基三甲基溴化铵(CTMAB)复配修饰膨润土吸附苯酚最佳修饰比例的基础上,通过添加膨润土改变2种黄棕壤中的蒙脱石含量(分别为6%和43%),利用X射线衍射和有机碳含量表征了蒙脱石含量对BS+CTMAB复配修饰黄棕壤性质的影响.同时,采用批处理法研究了蒙脱石含量对BS-12+CTMAB复配修饰黄棕壤吸附苯酚能力的影响,对比了不同温度、p H和离子强度下吸附的差异,并探讨了影响机制.结果表明,CTMAB复配修饰增加了BS-12修饰土样的TOC含量并增强了土样对苯酚的吸附能力,且苯酚在复配修饰土中的解吸程度均高于CK、BS-12和CTMAB修饰土;随着黄棕壤中蒙脱石含量的增大,BS-12、CTMAB修饰和BS-12+CTMAB复配修饰土蒙脱石层间距、TOC含量和对苯酚吸附能力整体上均呈增加趋势;单因素对各修饰土样吸附苯酚的影响程度上,温度、p H逐渐减小,离子强度逐渐增大;蒙脱石含量决定的TOC是影响修饰土样对苯酚吸附能力大小的关键因素,修饰土样对苯酚的吸附依然以分配作用为主.