长江中游城市群综合发展水平时空分异研究

区域可持续发展理念已被社会各界所接收,并逐步深入到社会发展计划及区域政策制定中。以区域差异分析为基础的区域格局优化是促进区域发展的核心内容。从经济发展、资源利用、环境保护、人口与公共服务和科技创新等5个方面选取23个指标,构建其监测评估指标体系综合分析长江中游城市群综合发展水平时空格局演变,有助于认清长江中游城市群综合发展格局形成的过程,出现的问题及产生的原因,从而制定相应的区域调控政策,这对于促进长江中游城市群内部区域之间协调发展及推进中部崛起战略具有重要的现实意义。基于2005年和2011年长江中游城市群37个地级市的统计数据,借助SPSS、GIS软件,采用全局主成分分析法评价分析其综合发展水平及时空分异,并对其成因进行分析。结果表明：区域综合发展分值有所提升,但增长潜力仍然很大;发展水平差异显著,且两极分化趋势明显;整体呈现出以武汉和长沙为中心,以南昌、合肥为副中心发展格局,但中心城市带动作用较弱,制约各城市群发展的因素各异。因此,未来长江中游城市群应努力提升区域经济发展总量的同时,转变经济产业结构,加强企业创新能力,寻求新的经济增长点。与此同时,应加大基础设施尤其是道路交通的投资强度;充分利用已有的地理区位及资源、科技人才优势发展第二、三产业,提高经济发展中资源的利用效率,降低能耗,保护环境;除此之外,还应加强区域宏观调控,注重城乡统筹发展,协调、平衡区域内部均衡发展,缩小区域之间及内部差异,促进技术转移和优势互补     

Evaluation of a Soil‐Based System to Dissipate Multiple Pesticides

Pesticide contaminated wastewater resulting from leftover mixes, equipment cleaning, and container disposal are problems related to pesticide use. This study reports on the effectiveness of a soil‐based bioreactor (SBBR) to dissipate pesticides of differing concentrations and mixtures. In order to accomplish this study, soil columns were used to simulate the SBBR. A mixture of five herbicides and two insecticides from seven different chemical families (atrazine, dicamba, fluometuron, metolachlor, sulfentrazone, chlopyrifus, and λ‐cyhalothrin) were added to the SBBR‐simulated system as formulated products in three concentrations each: 0 part per million (control), 10 ppm, and 100 ppm. Additionally a 1,000 ppm treatment was added that included just the five herbicides to investigate how the system would respond to heavy loading. The system was run for 90 days with samples taken at day 4 (just prior to loading the columns), then at 30, 60, and 90 days. At low pesticide concentrations (10 and 100 ppm), there was significant dissipation (p < 0.05) of all pesticides in the columns except sulfentrazone. At 1,000 ppm, fluometuron, in addition to sulfentrazone, did not show significant dissipation. Overall, the system performed as expected and could be considered practical for use on farms or nurseries. ©2015 Wiley Periodicals, Inc.     

Spatial mapping of city-wide PBDE levels using an exponential decay model

Passive air samplers (PAS) consisting of polyurethane foam (PUF) disks were deployed at 6 outdoor air monitoring stations in different land use categories (commercial, industrial, residential and semi-rural) to assess the spatial distribution of polybrominated diphenyl ethers (PBDEs) in the Brisbane airshed. Air monitoring sites covered an area of ~1143 km(2) and PAS were allowed to accumulate PBDEs in the city's airshed over three consecutive seasons commencing in the winter of 2008. The average sum of five (∑(5)) PBDEs (BDEs 28, 47, 99, 100 and 209) levels were highest at the commercial and industrial sites (12.7 ± 5.2 ng PUF(-1)), which were relatively close to the city center and were a factor of 8 times higher than residential and semi-rural sites located in outer Brisbane. To estimate the magnitude of the urban 'plume' an empirical exponential decay model was used to fit PAS data vs. distance from the CBD, with the best correlation observed when the particulate bound BDE-209 was not included (∑(5)-209) (r(2) = 0.99), rather than ∑(5) (r(2) = 0.84). At 95% confidence intervals the model predicts that regardless of site characterization, ∑(5)-209 concentrations in a PAS sample taken between 4-10 km from the city centre would be half that from a sample taken from the city centre and reach a baseline or plateau (0.6 to 1.3 ng PUF(-1)), approximately 30 km from the CBD. The observed exponential decay in ∑(5)-209 levels over distance corresponded with Brisbane's decreasing population density (persons/km(2)) from the city center. The residual error associated with the model increased significantly when including BDE-209 levels, primarily due to the highest level (11.4 ± 1.8 ng PUF(-1)) being consistently detected at the industrial site, indicating a potential primary source at this site. Active air samples collected alongside the PAS at the industrial air monitoring site (B) indicated BDE-209 dominated congener composition and was entirely associated with the particulate phase. This study demonstrates that PAS are effective tools for monitoring citywide regional differences however, interpretation of spatial trends for POPs which are predominantly associated with the particulate phase such as BDE-209, may be restricted to identifying 'hotspots' rather than broad spatial trends.     

铜对夏腊梅种子萌发及抗氧化酶活性的影响

采用室内水培试验,研究不同浓度的外源铜处理对夏腊梅(Sinocalycanthus chinensis)种子萌发、根伸长抑制率、呼吸强度、丙二醛及抗氧化酶系统的影响.结果表明,(1)铜浓度与夏腊梅根伸长抑制率呈显著正相关(P＜0.01),但与萌发率相关性不显著.(2)铜处理对夏腊梅种子的过氧化物酶(POD EC1.11.1.7)具有激活效应,且随着铜浓度的增加激活效应逐渐增强.丙二醛(MDA)含量随铜浓度的增大先略降而后逐渐升高.对超氧化物歧化酶(SOD EC 1.15.1.1)和过氧化氢酶(CAT EC 1.11.1.6)存在胁迫初期低浓度下的激活效应,随着铜浓度的增加及胁迫时间的延长,表现为抑制效应,且随着铜浓度的增加抑制效应逐渐增强.     

TiO2/膨润土纳米复合光催化剂降解偶氮染料的研究

采用酸性溶胶法合成TiO2 膨润土纳米复合光催化剂 ,并研究其光催化降解阳离子偶氮染料 .X射线衍射 (XRD)分析表明 ,TiO2 膨润土纳米复合物的d0 0 1衍射角为 9 0 6° .该复合催化剂具有较高的光催化降解有机污染物的活性 ,随着光照时间的延长 ,阳离子红GTL的特征峰 490 5nm强度逐渐减弱 ,最后它的特征峰可彻底消失 ,GTL的偶氮键是最活跃的化学键 ,它易于被氧化断键 .该复合催化剂的催化活性受溶液的pH影响较大 ,在中性和碱性条件下其光催化活性更强 .适量的过氧化氢可以加速光催化氧化反应 ,但过量的H2 O2 却抑制了羟基自由基的生成 ,从而使H2 O2 的利用效率下降 ,在本实验条件下其最佳用量是 6mmol L .     

Do evergreen and deciduous trees have different effects on net N mineralization in soil?

Evergreen and deciduous plants are widely expected to have different impacts on soil nitrogen (N) availability because of differences in leaf litter chemistry and ensuing effects on net N mineralization (N(min)). We evaluated this hypothesis by compiling published data on net N(min) rates beneath co-occurring stands of evergreen and deciduous trees. The compiled data included 35 sets of co-occurring stands in temperate and boreal forests. Evergreen and deciduous stands did not have consistently divergent effects on net N(min) rates; net N(min) beneath deciduous trees was higher when comparing natural stands (19 contrasts), but equivalent to evergreens in plantations (16 contrasts). We also compared net N(min) rates beneath pairs of co-occurring genera. Most pairs of genera did not differ consistently, i.e., tree species from one genus had higher net N(min) at some sites and lower net N(min) at other sites. Moreover, several common deciduous genera (Acer, Betula, Populus) and deciduous Quercus spp. did not typically have higher net N(min) rates than common evergreen genera (Pinus, Picea). There are several reasons why tree effects on net N(min) are poorly predicted by leaf habit and phylogeny. For example, the amount of N mineralized from decomposing leaves might be less than the amount of N mineralized from organic matter pools that are less affected by leaf litter traits, such as dead roots and soil organic matter. Also, effects of plant traits and plant groups on net N(min) probably depend on site-specific factors such as stand age and soil type.     

Occurrence of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in Lake Maggiore (Italy and Switzerland)

Samples of air (gas and particulate phases), bulk deposition, aquatic settling material and sediments were collected in Lake Maggiore (LM) in order to determine their content of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs). Air (gas and particulate phases) concentrations were 0.5 pg m(-3), 80 pg m(-3), 13 pg m(-3) and 106 pg m(-3) for SigmaPCDD/Fs, SigmaPCBs, Sigma dioxin-like PCBs (DL-PCBs) and SigmaPBDEs, respectively. Deposition fluxes ranged from 0.7 ng m(-2) d(-1) for SigmaPCDD/Fs to 32 ng m(-2) d(-1) for SigmaPCBs. Aquatic settling material presented concentrations of 0.4 ng g(-1) dry weight (dw) for SigmaPCDD/Fs, 13 ng g(-1) dw for SigmaPCB, 3.4 ng g(-1) dw for SigmaDL-PCBs and 5.7 ng g(-1) dw for SigmaPBDEs. Mean sediment concentrations were 0.4 ng g(-1) dw for SigmaPCDD/Fs, 11 ng g(-1) dw for SigmaPCB, 3 ng g(-1) dw for SigmaDL-PCBs and 5.1 ng g(-1) dw for SigmaPBDEs. Similar PCDD/F and DL-PCB congener patterns in all the environmental compartments of LM point to an important, if not dominant, contribution of atmospheric deposition as source of these pollutants into LM. In contrast, PBDE congener distribution was not similar in the different environmental compartments. BDE 47 dominated air and settling material, while BDE 209 was the predominant congener in the bulk atmospheric deposition. Moreover, sediments showed two distinct PBDE congener profiles. Lower PBDE concentrated sediments were dominated by congeners 47 and 99, while BDE 209 dominated in higher PBDE concentrated samples. This suggests the influence of local sources as well as atmospheric input of PBDEs into LM.     

钒和钨负载量对V2O5-WO3/TiO2表面形态及催化性能的影响

采用浸渍法制备了一系列不同钒和钨负载量的V₂O₅-WO₃/TiO₂催化剂样品,对样品NH₃选择性催化还原NO性能进行了评价,并用BET、XRD、XPS等手段对催化剂样品的表面形态进行了表征.研究发现,钒的负载量对催化剂的比表面积和催化活性有显著影响,当钒负载量从1％升高到8％时,催化剂比表面积下降了16 m²/g,最高活性温度降低了约100℃.钨起到稳定剂和助剂的双重作用,当钒负载量为1％时,钨负载量从0升高到6％,催化剂比表面积仅下降了3 m²/g,而活性温度窗口向高温和低温各拓宽了约50℃.研究表明钒和钨负载量都能影响催化剂表面的VO_x物种,但对催化剂的表面晶型没有明显影响.     

A(sⅢ)和A(sⅤ)对小球藻(Chlorella sp).的生长影响研究

砷是广泛存在于自然界中最常见的毒性污染物,包括土壤,沉积物,水体,大气层,甚至生物体,毒性极强。环境中砷的污染严重威胁人类的健康,已被视为一个全球性的公共卫生问题。为了研究砷对小球藻的生长影响,文章通过实验室培养方式,选取了6个不同浓度的As(Ⅲ()0.5、1.0、2.0、5.0、10.0、20.0 mg/L)和As(Ⅴ()1.0、5.0、10.0、20.0、50.0、100.0 mg/L)的培养处理,以在680 nm下小球藻的吸光度(OD680)作为衡量因子,对小球藻Chlorella sp(.100 ai)在不同浓度砷离子的培养液中的细胞密度进行了试验,整个实验共进行了7 d。结果表明,As(Ⅲ)和As(Ⅴ)浓度分别在10.0 mg/L和20.0 mg/L以上时抑制100 ai细胞生长,导致其密度下降。用概率统计方法计算得到A(sⅢ)对100 ai的96 h半数有效抑制浓度EC50值为25.79 mg/L。参照藻类生长抑制评价标准,A(sⅢ)对100 ai的毒性比A(sⅤ)大。