Ecological citizenship and democracy: Communitarian versus agonistic perspectives

Grassroots environmental movements have recently started to question the focus on sustainable consumption as a main strategy to tackle climate change. They prefer to address individuals as citizens rather than as consumers, and focus on collective rather than individual change. Two prominent movements in this regard are Transition Towns and Climate Justice Action. While both movements criticise conventional approaches, they put forward entirely different strategies for what has to happen instead. Based on extensive qualitative research, this article analyses how these movements manifest themselves in Flanders (Belgium). The focus is on their different accounts of how and why collective practices have to be built, and the place they attribute to ‘the political’ in this. The analysis reveals the existence of two different forms of ecological citizenship: one communitarian, the other agonistic.     

固相微萃取-气相色谱法测定生活污水中壬基酚

采用固相微萃取-气相色谱法测定生活污水中的壬基酚,优化了萃取纤维涂层材料、萃取时间与温度、解析时间与温度、盐度、pH值、搅拌速度等试验参数。方法在0.001mg／L-1.00mg／L范围内线性良好,检出限为0.0006mg／L,标准溶液平行测定的RSD为7.6％,生活污水加标回收率为42.7％-74.0％。     

固相微萃取-气相色谱/质谱联用法测定饮用水中苯类化合物

用固相微苹取(ＳＰＭＥ)－气相色谱/质谱联用法测定饮用水中苯类化合物,以１００μｍ ＰＤＭＳ(聚二甲基硅氧烷)萃取针提取、浓缩、分离与测定九种目标化合物．萃取时间经优化选定为８ｍｉｎ,而热解析时间设定为２ｍｉｎ． 本方法的相对标准偏差小于５%,线性范围宽(２０ｎｇ·ｍｌ－１－１００００ｎｇ·ｍｌ－１),多数化合物的检测限低于５μｇ·ｌ－１．饮用水样品检测显示,样品加标回收率范围在８４%至１１０%内．     

Three-fluid retention in porous media involving water, PCE and air

A classical way to obtain three-fluid retention curves in porous media from measured two-fluid retention curves is based on the Leverett concept, which states that the total volumetric liquid content in a water-wet porous medium, containing water, a nonaqueous-phase liquid (NAPL) and air, is a function of the capillary pressure across the interface between the continuous NAPL and air. This functional relationship results from the assumed condition that in a three-fluid porous medium, the intermediate wetting fluid spreads over the water-air interface. Application of Leverett's concept may not be valid, however, for nonspreading NAPLs like perchloroethylene (PCE). This paper discusses measurements of both PCE-air and water-PCE-air retention curves using a long vertical column in conjunction with a dual-energy gamma radiation system. The data indicate that the Leverett concept was applicable only until a critical PCE saturation had been reached.     

气质联用分析加硫酸化污泥中的有机酸

分别采用两种前处理方法分离富集加硫酸化污泥中的有机酸.方法一,利用阴离子交换树脂分离富集有机酸,在不洗脱的情况下直接和乙醇进行酯化反应,然后进行气质联用分析;方法二,利用活性炭纤维吸附型固相微萃取(ACF-SPME)的方法,顶空萃取分离后进行气质联用分析.两种方法的分析结果都未检测到酸化污泥中存在短链的有机酸,只检测到个别长链的和带苯环结构的有机酸.     

气相分子仪测定水中的硫化物

用气相分子吸收光谱仪测定水中的硫化物，对其工作曲线、精密度等进行了试验，表明方法简便、快捷、精密度、准确度都较好，适用于各种水质硫化物的测定。     

Study of metabolites from the degradation of polycyclic aromatic hydrocarbons (PAHs) by bacterial consortium enriched from mangrove sediments

The PAH metabolites produced during degradation of fluorene, phenanthrene and pyrene by a bacterial consortium enriched from mangrove sediments were analyzed using the on-fiber silylation solid-phase microextraction (SPME) combining with gas chromatography–mass spectrometry (GC–MS) method. Seventeen metabolites at trace levels were identified in different PAH degradation cultures based on the full scan mass spectra. In fluorene degradation cultures, 1-, 2-, 3- and 9-hydroxyfluorene, fluorenone, and phthalic acid were detected. In phenanthrene and pyrene degradation cultures, various common metabolites such as phenanthrene and pyrene dihydrodiols, mono-hydroxy phenanthrene, dihydroxy pyrene, lactone and 4-hydroxyphenanthrene, methyl ester, and phthalic acid were found. The detection of various common and novel metabolites demonstrates that SPME combining with GC–MS is a quick and convenient method for identification as well as monitoring the real time changes of metabolite concentrations throughout the degradation processes. The knowledge of PAH metabolic pathways and kinetics within indigenous bacterial consortium enriched from mangrove sediments contributes to enhance the bioremediation efficiency of PAH in real environment.     

中国碳排放强度的时空演进及跃迁机制

面对气候变化所带来的生存危机以及环境治理的复杂状况,对中国碳排放强度时空演进的动态监测与预警治理的研究是实现碳排放强度下降目标的关键。文章测算1997—2015年中国大陆30个省区碳排放强度的空间面板数据,采用探索性时空数据分析(ESTDA)方法对中国碳排放强度的空间相关性、集聚特征及其时空跃迁进行空间统计分析,借助分位数回归与时空跃迁嵌套模型,揭示在时间和空间推移的双重作用下中国各省区碳排放强度的时空跃迁机制。研究结果表明:(1)中国30个省区的碳排放强度在时空分布上并不是完全随机状态,各个省区碳排放强度之间具有显著的空间相关性特征,碳排放强度的变动趋势会受到其相临近省区碳排放强度的影响,省域间的碳排放强度在空间分布上呈现"集聚"与"分异"并存的时空演进特征。(2)中国碳排放强度空间集聚趋势增强,具有高度的凝固性和较低的流动性,10个高碳排放强度省区碳排放强度的稳定性将成为制约中国碳排放强度整体跃迁的重点省区,相关省区的跃迁性将成为驱动中国碳排放强度整体跃迁的关键省区。(3)各省区的碳排放强度空间集聚过程中存在时空跃迁的驱动模式和制约模式,分位数回归模型能够很好地解释各驱动因素对碳排放强度时空跃迁的驱动机制,不同响应阶段的驱动因素的分位数与碳排放强度时空跃迁类型之间具有很强的嵌套性。(4)根据各省区碳排放强度时空演进及其跃迁机制的分析结果,进一步提出加强对关键省区碳排放强度的有效监测与治理,加大碳排放的约束力度等差异化的碳减排调控措施。