湖北省"两圈"生物资源生态足迹动态分析

本文对1998-2008年湖北省武汉城市圈和鄂西生态文化旅游圈的生物资源生态足迹及其组成、人均生物资源生态足迹、生物资源生态承载量和生物资源生态赤字(盈余)进行了动态分析.研究表明,武汉城市圈生物资源生态足迹组成以耕地为主,其他生态生产性用地的足迹比例较小,各市州生物资源生态足迹整体呈现逐年增加的趋势,人均生物资源生态足迹小于省均值,生物资源生态承载量先升高后降低,各市州生物资源生态承载量由大到小排序为:黄冈、孝感、武汉、咸宁、天门、黄石、仙桃、鄂州、潜江,生态赤字呈增大趋势;鄂西生态圈除神农架外其他各市州的生物资源生态足迹均较大,林地足迹占主要地位,其总量对全省的贡献较大;人均生物资源生态足迹大于省均值,生物资源生态承载量呈增高趋势,各市州由大到小排序为:宜昌、十堰、襄樊、荆州、恩施、随州、荆门、神农架,该圈一直保持很高的生物资源生态盈余,但盈余值有减小的趋势.     

中国碳捕集、利用与封存技术研发与示范

碳捕集、利用与封存(CCUS)是一项新兴的、具有大规模减排潜力的技术,有望实现化石能源使用的CO2近零排放,被认为是进行温室气体深度减排最重要的技术路径之一.开展CCUS技术的研发和储备,将为中国未来温室气体减排提供一种重要的战略性技术选择,受到政府、企业和学术界的广泛关注.本文从CCUS技术产生和发展的背景出发,概括了该技术的特点及存在的主要同题,总结了当前中国CCUS技术政策,介绍了中国CCUS技术研发、试点示范、国际合作等的开展情况,并通过与欧美等发达国家CCUS技术发展与示范活动现状的对比,初步分析了中国CCUS技术发展方面存在的主要不足.为进一步推动我国CCUS技术的研发与示范,文章提出应加强国家层面的技术政策指导和宏观协调、引导资源有效配置;推动建设行业间的CCUS技术合作平台;重视CCUS来来技术应用软环境建设等有针对性的建议.     

香港典型地质遗迹资源与地质公园建设

香港素以金融、商业贸易中心闻名于世界,但香港境内所发育的曲折有致的岩石海岸、幽远宁静的海滩、巍峨多姿的群山、造型奇异的岛礁,弥足珍贵的自然生态和地质遗迹资源却鲜为人知。本文在对香港地质概况进行简单介绍的基础上,对香港地质遗迹资源进行系统分类和对比分析,指出西贡万宜水库至果洲群岛方圆近150 km2范围内发育的十分典型、极具规模的六方柱状节理构造景观是世界上同类岩石中罕见的地质现象,其分布面积大,露头完整,具有稀缺性、独特性和典型性,最后对香港国家地质公园一个公园,两个园区,八个景区的空间结构及每个园区的主要地质遗迹资源进行了系统归纳总结。香港国家地质公园的建立很好的起到了保育地质多样性的首要目标,同时很好地推动了香港的地质教育和科普发展。     

CGE Simulation for Levying Carbon Tax in China and International Experience of Levying Carbon Tax

Levying carbon tax is conducive to reducing carbon dioxide emissions and protecting the environment.The author firstly reviewed some relevant empirical studies on carbon tax both home and abroad,and then established the CGE model and simulated levying carbon tax in China.The study found that levying carbon tax would have little impact on China’s economy:in a short-term,China’s GDP might decrease by 0.51%,while in a long-term it might decrease by 0.08%;however,the carbon dioxide emissions would be substantially reduced.Meanwhile,levying carbon tax has some negative impact on the output of each industry in the very economic structure;of this,the mineral extractive industries would be influenced the most.Then the author summarized experience of levying carbon tax in foreign countries.     

上海城市样带土壤有机碳空间变异性研究

为揭示城市化、工业化等人为活动对土壤有机碳的影响,选择能反映上海城郊乡梯度差异的城市样带,采用地统计学方法对表层土壤样品土壤有机碳的空间变异结构和分布格局进行了分析。结果表明：城市表层土壤有机碳含量均属中等变异,徐汇区土壤有机碳含量呈正态分布,奉贤区、闵行区和所研究样带土壤有机碳含量呈对数正态分布。半方差函数模型拟合结果显示徐汇和闵行区土壤有机碳符合指数模型,奉贤和所研究样带土壤有机碳符合球状模型。通过泛克里格插值得到城市表层土壤有机碳含量空间分布图,发现徐汇、闵行区土壤有机碳呈岛状,奉贤区呈条带状,而所研究样带呈条带和岛状分布相结合的特点。土壤有机碳含量城郊乡梯度差异明显,工业化、城市化、肥料投入与管理等人为因素对城市土壤有机碳空间分布密切相关     

Aggregation and ecotoxicity of CeO₂ nanoparticles in synthetic and natural waters with variable pH, organic matter concentration and ionic strength

The influence of pH (6.0-9.0), natural organic matter (NOM) (0-10 mg C/L) and ionic strength (IS) (1.7-40 mM) on 14 nm CeO₂ NP aggregation and ecotoxicity towards the alga Pseudokirchneriella subcapitata was assessed following a central composite design. Mean NP aggregate sizes ranged between 200 and 10000 nm. Increasing pH and IS enhanced aggregation, while increasing NOM decreased mean aggregate sizes. The 48 h-E_rC20s ranged between 4.7 and 395.8 mg CeO₂/L. An equation for predicting the 48 h-E_rC20 (48 h-E_rC20 = −1626.4 × (pH) + 109.45 × (pH)² + 116.49 × ([NOM]) − 14.317 × (pH) × ([NOM]) + 6007.2) was developed. In a validation study with natural waters the predicted 48 h-E_rC20 was a factor 1.08-2.57 lower compared to the experimental values.     

Sequestration of organochlorine pesticides in soils of distinct organic carbon content

In the present study, five soil samples with organic carbon contents ranging from 0.23% to 7.1% and aged with technical dichlorodiphenyltrichloroethane (DDT) and hexachlorocyclohexane (HCH) for 15 months were incubated in a sealed chamber to investigate the dynamic changes of the OCP residues. The residues in the soils decreased over the incubation period and finally reached a plateau. Regression analysis showed that degradable fractions of OCPs were negatively correlated with soil organic carbon (SOC) except for α-HCH, while no correlation was found between degradation rate and SOC, which demonstrated that SOC content determines the OCP sequestration fraction in soil. Analysis of the ratio of DDT and its primary metabolites showed that, since it depends on differential sequestration among them, magnitude of (p,p′-DDE + p,p′-DDD)/p,p′-DDT is not a reliable criterion for the identification of new DDT sources.     

Photochemical processing of aldrin and dieldrin in frozen aqueous solutions under arctic field conditions

Organochlorine (OC) contaminants are transported to the Polar Regions, where they have the potential to bioaccumulate, presenting a threat to the health of wildlife and indigenous communities. They deposit onto snowpack during winter, and accumulate until spring, when they experience prolonged solar irradiation until snowmelt occurs. Photochemical degradation rates for aldrin and dieldrin, in frozen aqueous solution made from MilliQ water, 500 μM hydrogen peroxide solution or locally-collected melted snow were measured in a field campaign near Barrow, AK, during spring-summer 2008. Significant photoprocessing of both pesticides occurs; the reactions depend on temperature, depth within the snowpack and whether the predominant phase is ice or liquid water. The effect of species present in natural snowpack is comparable to 500 μM hydrogen peroxide, pointing to the potential significance of snowpack-mediated reactions. Aldrin samples frozen at near 0 °C were more reactive than comparable liquid samples, implying that the microenvironments experienced on frozen ice surfaces are an important consideration.     

Arsenic strongly associates with ferrihydrite colloids formed in a soil effluent

Arsenic mobility may increase in liquid phase due to association with colloidal Fe oxides. We studied the association of As with Fe oxide colloids in the effluent from water-saturated soil columns run under anoxic conditions. Upon exfiltration, the solutions, which contained Fe²⁺, were re-aerated and ferrihydrite colloids precipitated. The entire amount of effluent As was associated with the ferrihydrite colloids, although PO₄³⁻, SiO₄⁴⁻, CO₃²⁻ and dissolved organic matter were present in the effluent during ferrihydrite colloid formation. Furthermore, no subsequent release of As from the ferrihydrite colloids was observed despite the presence of these (in)organic species known to compete with As for adsorption on Fe oxides. Arsenic was bound via inner-sphere complexation on the ferrihydrite surface. FTIR spectroscopy also revealed adsorption of PO₄³⁻ and polymerized silica. However, these species could not impede the quantitative association of As with colloidal ferrihydrite in the soil effluents.