建设工程安全事故统计分析与安全管理对策研究

统计了112起建设工程事故,分析表明建设工程安全事故具有事故类型集中、承包商事故多发、检修及改造工程危险性较大、特殊作业管理不到位等特点和原因。提出了建设工程安全管理对策:开展安全文化建设,营造安全氛围;加强培训教育,提高参建人员尤其是施工操作人员的安全意识、技能水平;加大监管、惩戒力度,提高承包商违规成本;落实特殊作业各环节的管理。     

淮河流域安徽段水体和沉积物微塑料赋存特征及风险评估

为探究淮河流域安徽段水体与沉积物微塑料赋存特征及生态风险级别,采用野外采样、体式显微镜、扫描电镜、傅里叶红外光谱（FTIR）以及风险指数（H）和污染负荷指数（PLI）模型等方法,分析了流域水体和沉积物微塑料现状,并进行了微塑料生态风险评估.结果表明,流域各点位微塑料检测率为100%,表层水与沉积物微塑料平均丰度分别为（39800±3367） n ·m^-3和（5078±447） n ·kg^-1,下游微塑料平均丰度要高于上游和中游.水体和沉积物微塑料粒径以20~150 μm为主,占比分别为82.96%和80.77%.微塑料形状主要为纤维（水体76.05%、沉积物84.53%）、薄膜（水体21.83%、沉积物15.43%）和碎片（水体2.12%、沉积物0.04%）.水体和沉积物中微塑料主要以透明颜色为主,占比分别为63.31%和83.69%.水体和沉积物主要以聚乙烯（水体65.74%、沉积物80.62%）和聚丙烯（水体18.43%、沉积物9.71%）为主,微塑料主要来源于农业薄膜、废弃渔具渔网和港口人为废弃的塑料袋.微塑料风险指数（H）模型评估表明部分点位风险指数较高,淮河流域安徽段微塑料风险等级为Ⅱ级,污染负荷指数（PLI）模型评估表明流域地表水体和沉积物总体上生态风险较低.     

南洋楹根瘤菌株分离和应用的研究初报

南洋楹根瘤菌株分离和应用的研究初报潘超美，杨风，李幼菊（广东省土壤研究所，广州５１０６５０）ＰｒｅｌｉｍｉｎａｒｙＳｔｕｄｙｏｎＩｓｏｌａｔｉｏｎａｎｄＡｐｐｌｉｃａｔｉｏｎｏｆＮｏｄｕｌｅＢａｃｔｅｒｉａＳｔｒａｉｎｓｏｆＡｌｂｉｚｉａＦａｌｃａｔ...     

论生态农业与中国农业现代化

本文首先分析了我国农业生态环境存在的一系列严重问题，潜伏着巨大的危机。继而指出造成这种现象的原因是多方面的，既有不可忽视的自然因素，更有人为作用的因素。既有历史原因，也有现实障碍。京山县生态环境建设案例的剖析再一次证明生态农业是我国农业现代化的必然选择。最后本文在分析我国生态农业建设障碍因素的基础上，提出了发展生态农业的对策措施。     

中美气候变化论坛

由美国加州大学伯克利分校和北京大学联合主办的中美气候变化论坛于5月23日至24日在旧金山开幕．有来自中美两国以及欧洲等地的专家学者近200人参加了论坛。     

中国乡村发展面临的挑战与长期性管理策略

分析研究了当前我国乡村发展所面临的严峻的挑战性问题，如乡村非农化进程停滞，城乡差异扩大带来的问题等；尤其是乡村生态破坏和环境污染危及到农业生产环境的安全和城乡居民的生存基础的情况，指出21世纪中国乡村发展相当迫切而艰巨；在可持续发展思想的框架下，提出了长期性管理策略，即类型管理、目标管理、乡村制度性投入的管理模式，并考虑了实现乡村可持续发展的制度创新与保障问题；随后针对乡村发展管理，构想了实施对策：即，1）积极推进城市化，缩减乡村人口总量；2）开展农业行业标准的制定和修订工作；3）推进乡村产业的科技创新步伐；4）强化生态环境观念，实行空间开发管制、尤其是生态脆弱地区。此外还需强调环境教育机制和广泛的公众参与机制。     

旅游业推行清洁生产与可持续旅游发展

本文尝试将清洁生产的理论与方法导入旅游业 ,探讨了旅游业清洁生产的概念、必要性、内容和模式 ,进而就旅游业清洁生产与可持续旅游发展的关系及清洁生产的实施途径进行了探讨     

Adsorption of arsenate on soils. Part 2: modeling the relationship between adsorption capacity and soil physiochemical properties using 16 Chinese soils

An attempt has been made to elucidate the effects of soil properties on arsenate adsorption by modeling the relationships between adsorption capacity and the properties of 16 Chinese soils. The model produced was validated against three Australian and three American soils. The results showed that nearly 93.8% of the variability in arsenate adsorption on the low-energy surface could be described by citrate-dithionite extractable Fe (Fe(CD)), clay content, organic matter content (OM) and dissolved organic carbon (DOC); nearly 87.6% of the variability in arsenate adsorption on the high-energy surface could be described by Fe(CD), DOC and total arsenic in soils. Fe(CD) exhibited the most important positive influence on arsenate adsorption. Oxalate extractable Al (Al(OX)), citrate-dithionite extractable Al (Al(CD)), extractable P and soil pH appeared relatively unimportant for adsorption of arsenate by soils.     

Reductive dechlorination of 1,2,4-trichlorobenzene with palladized nanoscale Fe(zero-valent) particles supported on chitosan and silica

In this study, nanoscale Pd-Fe particles, with diameters less than 100 nm, were synthesized and dispersed over the chitosan and silica supports. Three different Pd-Fe particles were synthesized, namely 0.1% Pd-Fe, 0.5% Pd-Fe and 1.0% Pd-Fe. SEM images confirmed that the Pd-Fe particles were dispersed over the surface of the supports while SEM-EDX confirmed evenly distribution of Pd over Fe(zero-valent). alpha-Fe(zero-valent) crystallites were identified by means of XRD and observed in TEM. Reductive dechlorinations of 1,2,4-trichlorobenzene (1,2,4-TCB) with the nanoscale Pd-Fe/chitosan and Pd-Fe/silica were carried out in the batch experiment system. Disappearance of the parent species and formation of the reaction intermediates and end product were monitored at discrete times. The results show that the nano-scale Pd-Fe particles were able to completely dechlorinate the chlorinated benzenes within a very short timescale. Complete dechlorinations of 1,2,4-TCB to benzene were achieved within 60 min with the 1.0% Pd-Fe/chitosan and within 100 min with the 1.0% Pd-Fe/silica. Reaction rates were observed to increase with increasing Pd content of the Pd-Fe/support. The reactions apparently followed pseudo-first-order kinetics with respect to the 1,2,4-TCB transformation. A kinetic model is constructed to fit the experimental results for the reactions, enabling identification of the major and minor dechlorination pathways of 1,2,4-TCB. The model suggests that the 1,2,4-TCB transformation mainly followed the primary pathway of direct reductive dechlorination to benzene and secondary pathway of sequential hydrogenolysis to 1,2-dichlorobenzene (1,2-DCB) and then chlorobenzene (CB) or benzene.