哈长城市群县域碳排放空间溢出效应及影响因素研究——基于NPP-VIIRS夜间灯光数据的实证

基于2012-2016年NPP-VIIRS夜间灯光数据测算哈长城市群共计68个县级单元碳排放数据,采用空间自相关、位序规模法则、空间计量模型以及空间马尔科夫链模型,对县级尺度城市碳排放空间特征、影响因素和动态空间溢出作用进行分析.结果表明：①城市碳排放呈现逐年下降的趋势,空间Moran''s I指数表明研究区城市碳排放存在高度的空间自相关,碳排放的高值集聚性呈降低的趋势.②位序规模法则表明,研究区全部城市的碳排放属于次位型分布,高位次城市的碳排放表现突出;在前十位城市的碳排放规模先减少再增加,由分散向集中演变.③多种空间面板模型对比分析表明,城市经济水平和人口密度因素呈现显著的正相关关系;固定投资和外商投资因素仅在时间固定模型中起到正向影响作用;技术进步以及路网密度因素则起到显著的抑制作用.④空间马尔科夫链分析结果表明,城市碳排放空间溢出效应明显,位于低水平区域与高水平区域的城市在转移过程中保持稳定;位于中低水平区域的城市与高碳排放的城市相邻会降低转移概率,反之则会提升转移概率.     

基于LOADEST和数字滤波的水源地基流氮素输出定量方法应用实例

地表直接径流和基流均是流域非点源氮/磷养分输出的重要水文途径.科学认识和定量模拟基流氮/磷养分输出对于准确解析水源地水体非点源污染来源至关重要.基于Load Estimator模型和数字滤波算法,建立了定量水源地基流氮素输出的方法体系.以浙江省珊溪水源地的玉泉溪流域为例,利用玉泉溪2010-01—2013-12期间逐月总氮(TN)水质监测数据和逐日流量数据,展示了该方法的计算过程.结果表明,本文建立的水源地基流氮素输出定量方法结果合理,模拟精度高,决定系数和纳什系数分别为0.83和0.80;玉泉溪流域2010—2013年TN负荷量为141.21～274.68 t·a~(-1),平均208.63 t·a~(-1),年基流TN负荷量为84.39～168.68 t·a~(-1),平均127.69 t·a~(-1);基流对玉泉溪年均TN负荷量贡献率高达60%以上,流域基流养分输出对地表水体的污染应引起足够重视.     

不同空间划分方式下袁河流域景观结构对水质的影响

近年来景观结构的水文效应受到关注,研究不同空间划分方式下景观结构对河流营养盐、重金属变化的影响机制对于流域生态保护具有重要意义.本文于2018年7月和2019年1月在袁河干流及支流38个采样点采集水样,测定水体营养盐类污染指标（DO、NO₃^--N、NH₄⁺-N、TP和DOC浓度）和重金属类污染指标（Cr、Mn、Fe、Cu、Zn、As、Cd和Pb浓度）.基于前向变量选择、冗余分析等方法,筛选景观结构指标,量化其在不同尺度下对水体营养盐、重金属变化的影响.结果表明：①农田、斑块密度（PD）、斑块聚集指数（COHESION）及散布与并列指数（IJI）是影响水体营养盐变化的主要指标.林地、建设用地（Res）、平均最近邻体距离（ENN_MN）和最大斑块指数（LPI）的组合是影响重金属变化的主要指标.②在河岸缓冲带与圆形缓冲区划分方式下,景观结构均在100 m尺度对营养盐变化解释能力最强,平均解释率分别为31.5%、24.3%,均在1000 m尺度对重金属变化解释能力最强,平均解释率分别为32.0%、42.6%.③100 m河岸缓冲带和子流域尺度分别是景观结构影响水体营养盐、重金属变化的最佳空间尺度,平均解释率分别为31.5%、42.8%.以上结果表明,针对水体不同的污染类型,采用对应的划分方式及缓冲尺度有助于提高定量分析精度,为流域水环境保护、景观优化与管理提供科学依据.     

深圳湾流域面源与截排溢流污染特征及其对水环境的影响

随着点源污染逐步得到有效控制,面源与截排溢流污染对水环境的胁迫日益突出。基于土地遥感数据、城市排水管网等资料,构建流域—海湾一体化水环境模型,探讨深圳湾流域面源与截排溢流污染特征及其对水环境的影响,研究表明：（1）雨季COD、NH₃-N和TP单位面积面源与截排溢流污染负荷分别为17.21 t/km²与10.21 t/km²、0.17 t/km²与0.69 t/km²、0.04 t/km²与0.07 t/km²;（2）面源与截排溢流污染时间上主要集中于大雨及以上等级降水较多的5月和8月,空间上主要分布在截排工程集中、下垫面面积较大且坡度较陡的深圳河、大沙河和新洲河流域;（3）面源与截排溢流水体COD、NH₃-N和TP浓度可达地表水V类标准的3.7倍、18.2倍和8.5倍;（4）雨季COD、NH₃-N和TP浓度高于旱季的区域分别超过深圳湾总面积的40%、60%和65%。     

喜凉作物生长期对全球变暖停滞响应的时空差异——以中国绿洲为例

基于中国绿洲喜凉作物（chimonophilous crop）分布区39个站点1960~2016年逐日平均气温资料,运用线性趋势法、反距离加权插值（IDW）、Morlet小波、Mann-Kendall检验等方法,研究中国绿洲喜凉作物气候生长期的时空变化对变暖停滞的响应.结果表明：①变暖停滞期,中国绿洲喜凉作物气候生长期起、止日及生长期日数以-0.2d/10a、0.33d/10a、0.53d/10a的趋势变化,较1960~2016年起始日提前趋势减缓1.01d/10a,终止日推迟减缓1.28d/10a,生长期日数延长减缓2.3d/10a,对变暖停滞有响应.②中国绿洲喜凉作物气候生长期起始日对变暖停滞响应的站点有44%,终止日和生长期日数均为49%,主要分布在南疆、柴达木盆地和河西绿洲,其中河西绿洲对变暖停滞响应最明显,南疆次之,柴达木最小,而北疆绿洲不存在滞缓现象,显然空间差异明显.③M-K检验显示,中国绿洲喜凉作物气候生长期起、止日及生长期日数分别在2001年、1990年和1997年发生突变,起始日晚于变暖停滞起始年份,终止日和生长期日数早于变暖停滞起始年,且分绿洲生长期日数突变年与变暖停滞起始年相接近.④Morlet小波得出变暖停滞期其变化稳定存在2.4~4.3a的震荡周期,表明未来几年中国绿洲喜凉作物气候生长期仍持续延长.     

Regulated emission characteristics of in-use LNG and diesel semi-trailer towing vehicles under real driving conditions using PEMS

On-road driving emissions of six liquefied natural gas(LNG) and diesel semi-trailer towing vehicles(STTVs) which met China Emission Standard IV and V were tested using Portable Emission Measurement System(PEMS) in northern China.Emission characteristics of these vehicles under real driving conditions were analyzed and proved that on-road emissions of heavy-duty vehicles(HDVs) were underestimated in the past.There were large differences among LNG and diesel vehicles, which also existed between China V vehicles and China IV vehicles.Emission factors showed the highest level under real driving conditions, which probably be caused by frequent acceleration, deceleration, and start-stop.NOx emission factors ranged from 2.855 to 20.939 g/km based on distance-traveled and 6.719–90.557 g/kg based on fuel consumption during whole tests, which were much higher than previous researches on chassis dynamometer.It was inferred from tests that the fuel consumption rate of the test vehicles had a strong correlation with NOx emission, and the exhaust temperature also affected the efficiency of Selected Catalytic Reduction(SCR) aftertreatment system, thus changing the NOx emission greatly.THC emission factors of LNG vehicles were 2.012–10.636 g/km, which were much higher than that of diesel vehicles(0.029–0.185 g/km).Unburned CH_4 may be an important reason for this phenomenon.Further on-road emission tests, especially CH_4 emission test should be carried out in subsequent research.In addition, the Particulate Number(PN) emission factors of diesel vehicles were at a very high level during whole tests, and Diesel Particulate Filter(DPF)should be installed to reduce PN emission.     

Bioassay: A useful tool for evaluating reclaimed water safety

Wastewater reclamation and reuse has been proved to be an effective way to relieve the fresh water crisis. However, toxic contaminants remaining in reclaimed water could lead to potential risk for reuse, and the conventional water quality standards have difficulty guaranteeing the safety of reclaimed water. Bioassays can vividly reflect the integrated biological effects of multiple toxic substances in water as a whole, and could be a powerful tool for evaluating the safety of reclaimed water. Therefore, in this study, the advantages and disadvantages of using bioassays for evaluating the safety of reclaimed water were compared with those of conventional water quality standards. Although bioassays have been widely used to describe the toxic effects of reclaimed water and treatment efficiency of reclamation techniques, a single bioassay cannot reflect the complex toxicity of reclaimed water, and a battery of bioassays involving multiple biological effects or in vitro tests with specific toxicity mechanisms would be recommended. Furthermore, in order to evaluate the safety of reclaimed water based on bioassay results, various methods including potential toxicology, the toxicity unit classification system, and a potential eco-toxic effects probe are summarized as well. Especially, some integrated ranking methods based on a bioassay battery involving multiple toxicity effects are recommended as useful tools for evaluating the safety of reclaimed water, which will benefit the promotion and guarantee the rapid development of the reclamation and reuse of wastewater.     

Role of glycine on sulfuric acid-ammonia clusters formation: Transporter or participator

Glycine(Gly) is ubiquitous in the atmosphere and plays a vital role in new particle formation(NPF).However,the potential mechanism of its on sulfuric acid(SA)-ammonia(A)clusters formation under various atmospheric conditions is still ambiguous.Herein,a(Gly)_x·(SA)_y·(A)_z(z≤x+y≤3) multicomponent system was investigated by using density functional theory(DFT) combined with Atmospheric Cluster Dynamics Code(ACDC) at different temperatures and precursor concentrations.The results show that Gly,with one carboxyl(-COOH) and one amine(-NH_2) group,can interact strongly with SA and A in two directions through hydrogen bonds or proton transfer.Within the relevant range of atmospheric concentrations,Gly can enhance the formation rate of SA-A-based clusters,especially at low temperature,low [SA],and median [A].The enhancement(R) of Gly on NPF can be up to 340 at T=218.15 K,[SA]=10~4,[A]=10~9,and [Gly]=10~7 molecules/cm~3.In addition,the main growth paths of clusters show that Gly molecules participate into cluster formation in the initial stage and eventually leave the cluster by evaporation in subsequent cluster growth at low [Gly],it acts as an important "transporter" to connect the smaller and larger cluster.With the increase of [Gly],it acts as a "participator" directly participating in NPF.     

Adsorption of 17β-estradiol from aqueous solution by raw and direct/pre/post-KOH treated lotus seedpod biochar

Five biochars derived from lotus seedpod(LSP) were applied to examine and compare the adsorption capacity of 17β-estradiol(E2) from aqueous solution.The effect of KOH activation and the order of activation steps on material properties were discussed.The effect of contact time,initial concentration,p H,ionic strength and humic acid on E2 adsorption were investigated in a batch adsorption process.Experimental results demonstrated that the pseudo second-order model fitted the experimental data best and that adsorption equilibrium was reached within 20 hr.The efficiency of E2 removal increased with increasing E2 concentration and decreased with the increase of ionic strength.E2 adsorption on LSP-derived biochar(BCs) was influenced little by humic acid,and slightly affected by the solution p H when its value ranged from 4.0 to 9.0,but considerably affected at p H 10.0.Low environmental temperature is favorable for E2 adsorption.Chemisorption,π–π interactions,monolayer adsorption and electrostatic interaction are the possible adsorption mechanisms.Comparative studies indicated that KOH activation and the order of activation steps had significant impacts on the material.Post-treated biochar exhibited better adsorption capacity for E2 than direct treated,pretreated,and raw LSP biochar.Pyrolyzed biochar at higher temperature improved E2 removal.The excellent performance of BCs in removing E2 suggested that BCs have potential in E2 treatment and that the biochar directly treated by KOH would be a good choice for the treatment of E2 in aqueous solution,with its advantages of good efficiency and simple technology.     

Influence of floc dynamic protection layer on alleviating ultrafiltration membrane fouling induced by humic substances

Cake layer formation is inevitable over time for ultrafiltration (UF) membrane-based drinking water treatment. Although the cake layer is always considered to cause membrane fouling, it can also act as a “dynamic protection layer”, as it further adsorbs pollutants and dramatically reduces their chance of getting to the membrane surface. Here, the UF membrane fouling performance was investigated with pre-deposited loose flocs in the presence of humic acid (HA). The results showed that the floc dynamic protection layer played an important role in removing HA. The higher the solution pH, the more negative the floc charge, resulting in lower HA removal efficiency due to the electrostatic repulsion and large pore size of the floc layer. With decreasing solution pH, a positively charged floc dynamic protection layer was formed, and more HA molecules were adsorbed. The potential reasons were ascribed to the smaller floc size, greater positive charge, and higher roughness of the floc layer. However, similar membrane fouling performance was also observed for the negative and positive floc dynamic protection layers due to their strong looseness characteristics. In addition, the molecular weight (MW) distribution of HA also played an important role in UF membrane fouling behavior. For the small MW HA molecules, the chance of forming a loose cake layer was high with a negatively charged floc dynamic protection layer, while for the large MW HA molecules it was high with a positively charged floc dynamic protection layer. As a result, slight UF membrane fouling was induced.