三峡库区移民贫困致因的精准识别与减贫路径的实证研究

随着我国经济发展和扶贫成效的显现,老区、山区、民族地区和移民库区等集中连片的特殊贫困区已经成为我国当前精准扶贫的主战场。由于面临生产资料匮乏、生态环境恶化和地质灾害频发等恶劣环境,库区移民贫困问题已成为新时期扶贫攻坚最难啃的"硬骨头"。因此,开展库区移民贫困致因的精准识别与减贫路径研究具有重要的现实意义。基于对库区移民贫困现状的扎根理论分析,本文提出了分析农户生计的新框架。在此基础上,本文以三峡库区26个县(区)为研究对象,随机抽取4县(区)796户移民作为样本,首先,采用灰色关联分析法和熵权法对库区移民主要致贫因子进行挖掘;接着,采用PLS-SEM模型分析影响库区移民生计状况的关键因子和关键路径。研究表明:(1)三峡库区移民贫困现象仍很严重,患病、劳动能力弱和失地是移民致贫的三大主因。三峡库区仍有175.94万人生活在贫困线以下,三大致贫原因依次是:因病致贫26.49%、因劳动能力弱致贫22.10%和失地致贫21.65%。(2)心理资本可有效促进移民其他资本效能的发挥,对生计状况存在着显著的直接效应和间接效应。(3)在影响生计状况的四类资本中,人力资本对库区移民生计状况影响最大。基于以上发现,本文提出了实现库区移民精准脱贫的政策建议:(1)国家应高度重视三峡库区移民贫困问题,大力开展精准扶贫;(2)增加心理干预措施以提高移民心理资本存量,帮助移民摆脱心理贫困;(3)开展劳动力技能培训,提高库区移民人力资本水平。     

特朗普“去气候化”政策对全球气候治理的影响

美国特朗普政府宣布退出《巴黎协定》是当前全球气候治理中最受舆论关注的问题,对事态发展趋势的判断和事件影响的评估是最为亟需的。本文系统分析了特朗普政府上任后推行的一系列"去气候化"政策,以及其退出《巴黎协定》的主要动因和可能形式,同时量化评估了这些内政外交的"倒退"对美国实施国家自主贡献目标以及全球气候治理格局的实质影响,并据此提出了中国应对全球气候治理新形势变化的对策和建议。研究表明,特朗普政府"美国优先"的能源政策根植于复兴制造业和加大基础设施投资的经济利益动机,随着特朗普"去气候化"进程持续发酵,诸多气候政策面临存续风险,美国实施国家自主贡献将面临严峻挑战,"倒行政策"将有可能使美国温室气体排放出现反弹。如果不考虑中、高危气候政策,美国2025年温室气体排放也仅能相对2005年下降11.0%—14.9%,距离下降26%—28%的国家自主贡献目标相去甚远。同时,特朗普政府拒绝继续履行向发展中国家提供气候资金支持的义务,将有可能导致绿色气候基金拖欠资金总额上升117%,并进一步挫伤全球低碳投资的信心。没有美国的全球气候治理3.0时代将呈现出新的复杂特征,并不可避免地造成减排、资金和领导力缺口的持续扩大,也不排除后续会出现消极的跟随者,整体进程将可能进入一个低潮周期。虽然国际社会对中国引领全球气候治理充满期待,但中国仍应审慎对待,长远谋划应对气候变化的内政外交战略,而不应将"气候举旗"看作是一蹴而就的短期策略,对各种要求中国发挥"领导作用"的说法保持清醒头脑。在今后气候谈判中,美国仍有较大可能会二次"要价",中国作为排放大国的压力依然不容小觑,中美气候关系需要再定位。     

Urinary metabolomic profiling in rats exposed to dietary di(2-ethylhexyl) phthalate (DEHP) using ultra-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC/Q-TOF-MS)

Di(2-ethylhexyl) phthalate (DEHP) is an omnipresent environmental chemical with widespread nonoccupational human exposure through multiple ways. Although considerable efforts have been invested to investigate mechanisms of DEHP toxicity, the key metabolic biomarkers of DEHP toxicity remain to be identified. The aim of this study was to assess the urinary metabonomics of dietary DEHP in rats using the technique of ultra-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC/Q-TOF-MS). Fourteen female Wistar rats were divided into two groups and given increasing dietary doses of DEHP for 30 consecutive days. The urinary metabolite profile was studied using ultra-performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry. Principal component analysis (PCA) and partial least squares-discriminant analysis (PLS-DA) enabled clusters to be clearly separated. Eleven principal urinary metabolites were identified as contributing to the clusters. The clusters in the positive electrospray ionization (ESI) mode were xanthurenic acid, kynurenic acid, nonate, N6-methyladenosine, and L-isoleucyl-L-proline. The clusters in the negative ESI mode were hippuric acid, tetrahydrocortisol, citric acid, phenylpropionylglycine, cPA(18:2(9Z, 12Z)/0:0), and LysoPC(14:1(9Z)). The urinary metabonomic changes indicated that exposure to dietary DEHP can affect energy-related metabolism, liver and renal function, fatty acid metabolism, and cause DNA damage in rats. The findings of this study on the urinary metabolites and metabolic pathways of DEHP may form the basis for future studies on the mechanisms of toxicity of this commonly found environmental chemical.     

Multiple copper adsorption and regeneration by zeolite 4A synthesized from bauxite tailings

Copper ions were first adsorbed by zeolite 4A synthesized from bauxite tailings, the desorption of Cu(II) using Na₂EDTA solutions was performed, and the recycling of zeolite 4A in adsorption and desorption was systematically investigated. It was observed that the Cu(II) removal efficiency was directly dependent on the initial pH value. The maximum removal efficiency of Cu(II) was 96.2% with zeolite 4A when the initial pH value was 5.0. Cu(II) was completely absorbed in the first 30 min. It was also observed that the desorption efficiency and zeolite recovery were highly dependent on the initial pH and concentration of Na₂EDTA in the solution. The desorption efficiency and percent of zeolite recovered were 73.6 and 85.9%, respectively, when the Na₂EDTA solution concentration was 0.05 mol L^?1 and the pH value was 8. The recovered zeolites were pure single phase and highly crystalline. After 3 cycles, the removal efficiency of Cu(II) was as high as 78.9%, and the zeolite recovery was 46.9%, indicating that the recovered zeolites have good adsorption capacity and can repeatedly absorb Cu(II).

     

Dechlorination of hexachlorobenzene using lead–iron bimetallic particles

Synthesized lead–iron (Pb/Fe) bimetallic particles were applied to dechlorinate hexachlorobenzene (HCB) under various conditions (e.g. bimetal amount, initial pH value, reaction temperature, and reaction duration). The results showed that adding Pb onto Fe benefited the dechlorination of HCB and the bimetal with 1.4% Pb content performed best. The degradation rate decreased regularly as the initial pH value of the aqueous increased from 1.9 to 11.1 except for pH 7.0 where the fastest dechlorination rate emerged. The dechlorination could be enhanced by increasing the amount of Pb/Fe or the reaction temperature. The dechlorination ratio of HCB within 15 min increased from 24.3% to 81.3% when Pb/Fe amount increased from 0.1 g to 0.8 g. The dechlorination followed pseudo-first-order kinetics, and the dechlorination rate constants were 0.0027, 0.0064, 0.0157, and 0.0321 min^?1 at 25, 50, 70, and 85 °C, respectively, and the activation energy (E_a) of the dechlorination by Pb/Fe was 37.86 kJ mol^?1.     

化学沉淀法强化常规工艺应急去除水中的镉

在常规工艺基础上,通过投加氢氧化钠,实验进行了应急去除重金属镉的研究。实验结果表明,该方法能有效去除饮用水水源的镉,效果稳定,可进行应急处理。对pH、镉初始浓度和混凝剂投加量3个影响因素的灰色关联分析表明,3个因素对镉去除效果影响的大小排序为:滤后水pH>混凝剂投加量>镉初始浓度。在水源镉突发污染时,在原有常规水处理工艺基础上,通过控制滤后水pH可实现对重金属镉的去除,pH的控制值与水源水质有关。     

Origin and distribution of trace elements in high-elevation precipitation in southern China

Introduction

During a 2009 investigation of the transport and deposition of trace elements in southern China, 37 event-based precipitation samples were collected at an observatory on Mount Heng, China (1,269?m asl).

Methods

Concentrations of trace elements were analyzed using inductively coupled plasma?Cmass spectrometry and the wet deposition fluxes were established. A combination of techniques including enrichment factor analysis, principal component analysis, and back trajectory models were used to identify pollutant sources.

Results

Trace element concentrations at Mount Heng were among the highest with respect to measured values reported elsewhere. All elements were of non-marine origin. The elements Pb, As, Cu, Se, and Cd were anthropogenic, while Fe, Cr, V, Ba, Mn, and Ni were of mixed crustal/anthropogenic origin. The crustal and anthropogenic contributions of trace elements were 12.8 % (0.9?~?17.4 %) and 87.2 % (82.6?~?99.1 %), with the maximum crustal fraction being 17.4 % for Fe. Coal combustion, soil and road dust, metallurgical processes, and industrial activities contributed to the element composition.

Conclusions

Summit precipitation events were primarily distant in origin. Medium- to long-range transport of trace elements from the Yangtze River Delta and northern China played an important role in wet deposition at Mount Heng, while air masses from south or southeast of the station were generally low in trace element concentrations.     

山地城市暴雨径流污染特性及控制对策

为了解山城重庆的暴雨径流污染特性,充实国内仍然薄弱的基础资料,对4种用地类型的4场暴雨进行了监测,测试指标包括TSS、COD、TP、TN和NH3-N。结果表明,对于坡度2.5%的交通干道和坡度30%的校园人行道,从污染物浓度降幅的角度考虑初期径流的控制量应分别为2～3 mm和1.8 mm。随降雨时间的延长,路面污染物浓度迅速降低,坡度越大,降低速率越快。对于平均浓度,校园屋顶和草坪的各污染物浓度均达到地表水环境质量Ⅴ类标准(总氮和氨氮除外)。交通干道和校园人行道的总磷平均浓度也满足地表水环境质量Ⅴ类标准,但2种下垫面的COD、TN和氨氮平均浓度分别超出地表水环境质量Ⅴ类标准的2～8倍、1.9～3.1倍和1.9～4.3倍。对于交通干道,场次降雨径流的总氮、总磷和氨氮平均浓度与初期浓度的比值和污染物浓度20 min降幅接近(分别为0.5～0.53和50%～55%)接近,而COD和TSS平均浓度与初期浓度的比值和污染物浓度20 min降幅相近(分别为0.35～0.37和78%～84%)。对于校园人行道,污染物浓度20 min降幅均达到90%以上(90%～96%),场次降雨径流的总氮、总磷、氨氮、COD和TSS的平均浓度与初期浓度的比值接近(0.3～0.4)。研究结果为山地城市暴雨径流的污染控制提供了参考。     

微波诱导AC/Cu、AC/Fe催化非均相Fenton 反应催化降解垃圾渗滤液

采用活性炭载体负载Cu、Fe为催化剂,在微波诱导作用下,对垃圾渗滤液污染物进行降解。实验结果表明,活性炭负载金属前经适当浓度硝酸浸泡处理后,催化剂对COD去除率提高可超过15%,过高硝酸盐浓度对COD去除有不利影响;催化剂对COD去除率随Cu、Fe金属负载量增加呈先增加后降低的趋势,催化剂对Cu、Fe的最佳负载量分别为质量百分比2.11%和1.12%。对于AC-Cu体系,在初始pH=3,H2O2投加量为4.98×103mg/L,催化剂用量为5.0×103mg/L,420 W功率下微波辐射10 min时,垃圾渗滤液COD去除率可达到84.13%;对于AC-Fe体系,当H2O2投加量为0.33×103mg/L,催化剂AC-Fe用量为2.0×104mg/L,420 W功率下微波作用10 min时,垃圾渗滤液COD去除率为60.16%。分析2种催化剂对COD去除差异的原因,可能是催化剂AC-Cu表面单分子分布的阈值比AC-Fe高。降解液的pH值对AC-Cu体系、AC-Fe体系COD去除影响存在拐点,最高COD去除率点对应的降解液pH值为3。微波辐射功率较低时,体系COD去除率随辐射功率增加而增加;辐射功率较高时,高温下垃圾渗滤液中有机硫化物分解成小分子硫化物,对催化剂活性存在一定抑制作用。