乌江流域（四川部分）水土流失及其防治对策

根据径流场观测材料、调查资料及历史事实,论述了乌江流域(四川部分)的水土流失现状、特点、危害及导致水土流失的自然因素和人为因素。针对该流域水土流失特点和原因提出了防治对策。     

黔中石漠化地区不同土地利用方式对土壤环境的影响

在贵州省普定县喀斯特石漠化地区通过调查分析,对3种土地不同利用方式（Ⅰ封山育林地、Ⅱ退耕还林地、Ⅲ农耕地）土壤物理性质、化学性质及土壤种子库进行了研究。结果表明利用方式的不同对土壤物理性质、化学性质及土壤种子库均产生了显著的影响。土壤容重、土壤毛管孔隙度随土壤扰动的加剧而下降,表现为Ⅰ＞Ⅱ＞Ⅲ;土壤总孔隙度与非毛管孔隙度呈现出随土壤扰动程度增加而增加的趋势,表现为Ⅲ＞Ⅱ＞Ⅰ;不同层次之间容重的变异较小,土壤质地比较均一;Ⅱ土壤有机质低于类型Ⅲ和Ⅰ;Ⅰ初步形成了林地环境,林地土壤表现出良性转变。随土壤深度的增加,有机质、全氮、全磷、速效氮表现出减少的趋势,土壤扰动降低了土壤化学性质层次间变异。不同利用方式下土壤种子库物种组成变化不大,土壤中的种子集中分布在表层0～5 cm内,随土层的加深所含种子数量、物种数逐渐降低。不同利用类型的土壤种子数量在0～5 cm层次差异显著（〖WTBX〗p〖WTBZ〗=0.021 897）,种子种类差异不显著（〖WTBX〗p〖WTBZ〗=0.097 628）。土壤扰动促进种子向深层传播,退耕还林有利于土壤质量的恢复。     

腐殖酸对砂质土壤吸附Cr(VI)的影响

利用系列摇瓶振荡实验,研究了在砂质土壤介质中腐殖酸(HA)对Cr(VI)还原作用及增强土壤表面对其吸附的影响.通过改变反应接触时间、pH值、HA投加量等条件,确定了最佳吸附反应条件.结果表明:砂质土壤中存在HA时,可使Cr(VI)还原为毒性较小的Cr(Ⅲ),明显增强土壤对可溶态Cr离子的吸附能力,比同等条件下无HA的土壤吸附量增大1倍以上.一般整个反应过程约8 h即可达到稳定.pH值对Cr的还原和吸附有很大的影响,酸性条件下的吸附量比碱性条件可增大1倍,最佳pH值为2～4;当pH＞5时吸附能力急剧下降,pH=10时吸附去除量降为20%.有HA存在时砂质土壤土对Cr(VI)的吸附反应为一级动力学反应,K298=0.033 5 min-1,砂土对CrO2-4的等温吸附曲线较好地满足Langmuir公式.     

茶园土壤酸化对氟的影响及茶叶氟安全限量的探讨

在分析国内外茶园土壤酸化现状的基础上,概述了关于土壤水溶性氟与土壤pH值关系的研究进展,并通过实地调研和培养实验研究了茶园土壤酸化对土壤水溶性氟的影响.实地调研中土壤水溶性氟含量与土壤pH值无显著相关性.培养实验中,当pH＞4.00时,模拟土壤水溶性氟含量随土壤pH值的下降变化不显著;而当pH＜4.00时,土壤水溶性氟含量随着pH值的下降迅速增加,且达到极显著水平.同时描述了世界各国制订的每人每天最大摄氟量标准,对我国现行茶叶标准与国外一些国家的同类标准之间的差异做了评析.茶叶溶出实验的结果表明,我国茶叶氟安全限量需要进一步完善.     

长三角和珠三角土壤中汞的化学形态、转化和吸附特性

为了解长江三角洲和珠江三角洲农业土壤中汞的积累可能产生的环境影响,选择10个代表性农业土壤样品,研究了土壤中汞的化学形态、积累过程中形态的转化及吸附-解吸行为.研究表明,当无外源汞加入时,长江三角洲和珠江三角洲农业土壤中,汞主要以稳定的残余态形式存在.但随着汞加入量的增加,土壤中可交换态汞显著增加,增加程度与土壤性质有关.土壤pH是影响土壤汞有效性最重要的因素,其对土壤汞的吸附、解吸、形态转化和存在形态均有很大影响.土壤酸化可促进土壤汞的释放,加剧对环境的危害,防治土壤酸化也可有效降低土壤中汞对环境的危害.     

黑河中游边缘绿洲农田退耕还草的土壤碳、氮固存效应

研究黑河中游边缘绿洲农田退耕种植苜蓿5a后土壤碳、氮库的变化,通过对2个土类(开垦耕种的风沙土和灰棕漠土)退耕苜蓿地和相邻农田0～5、5～10和10～20cm土层土壤有机碳(SOC)和全氮(TN)、颗粒有机碳和氮(POC、PON)储量的分析表明:开垦耕种的风沙土和灰棕漠土有极低的SOC和TN含量,退耕种植苜蓿后0～20cm SOC储量提高了22.1%～27.8%,SOC的固存率平均为0.47 Mg/(hm²·a),0～5cm表层SOC储量变化最大,提高32%～66%;TN储量0～20cm储量变化不显著,在0～5cm表层TN储量风沙土和灰棕漠土分别提高12.8%和48.1%.退耕后POC和PON较SOC和TN有更显著的变化,其分配比例增加,0～20cm土层POC和PON储量分别提高22.8%～42.7%和18.6%～57.6%,在0～5cm变化最大;在瘠薄耕地转变为多年生苜蓿地后土壤C库的增加主要是由于POC的形成量增加.SOC含量相对更低的灰棕漠土比风沙土退耕后土壤C、N的增加更为明显.     

淮河上游全新世黄土-土壤剖面重金属元素分布与环境变化

在野外考察研究的基础上利用X-射线荧光光谱仪测定了河南禹州全新世YPC黄土-土壤剖面Zn、Cu、Co、Ni、Nb、Pb、V、Cr、Mn、Ti重金属元素的含量及其变化,研究表明在黄土堆积期,重金属元素的含量都很低,变化幅度也很小,可作为衡量古土壤层成壤改造的背景值.在全新世古土壤和现代表土中这些元素含量却大大增加,说明在温暖湿润的时期,成壤改造使易溶易迁移元素的淋失导致重金属元素的相对富集.而Pb含量从8cm深度处向上急剧增加,增幅达60%,这是大气污染物沉降积累的客观记录.     

Ecological effects of crude oil residues on the functional diversity of soil microorganisms in three weed rhizospheres

Ecological effects of crude oil residues on weed rhizospheres are still vague. The quantitative and diversity changes and metabolic responses of soil-bacterial communities in common dandelion （Taraxacum officinale）, jerusalem artichoke （Silphiurn perfoliatum L.） and evening primrose （A colypha australis L.） rhizospheric soils were thus examined using the method of carbon source utilization. The results indicated that there were various toxic effects of crude oil residues on the growth and reproduction of soil bacteria, but the weed rhizospheres could mitigate the toxic effects. Total heterotrophic counting colony-forming units （CFUs） in the rhizospheric soils were significantly higher than those in the non-rhizospheric soils. The culturable soil-bacterial CFUs in the jerusalem artichoke （S. perfoliatum） rhizosphere polluted with 0.50 kg/pot of crude oil residues were almost twice as much as those with 0.25 kg/pot and without the addition of crude oil residues. The addition of crude oil residues increased the difference in substrate evenness, substrate richness, and substrate diversity between non-rhizospheric and rhizospheric soils of T. officinale and A. australis, but there was no significant （p〉0.05） difference in the Shannon＇s diversity index between non-rhizospheric and rhizospheric soils of S. perfoliatum. The rhizospheric response of weed species to crude oil residues suggested that S. perfoliatum may be a potential weed species for the effective plant-microorganism bioremediation of contaminated soils by crude oil residues.     

Removal of heavy metals from a contaminated soil using tartaric acid

This study reports the feasibility of remediation of a heavy metal （HM） contaminated soil using tartaric acid, an environmentally-friendly extractant. Batch experiments were performed to test the factors influencing remediation of the HM contaminated soil. An empirical model was employed to describe the kinetics of riM dissolution/desorption and to predict equilibrium concentrations of HMs in soil leachate. The changes of HMs in different fractions before and after tartaric acid treatment were also investigated. Tartaric acid solution containing HMs was regenerated by chestnut shells. Results show that utilization of tartaric acid was effective for removal of riMs from the contaminated soil, attaining 50%-60% of Cd, 40%-50% of Pb, 40%-50% of Cu and 20%-30% of Zn in the pH range of 3.5-4.0 within 24 h. Mass transfer coefficients for cadmium （Cd） and lead （Pb） were much higher than those for copper （Cu） and zinc （Zn）. Sequential fractionations of treated and untreated soil samples showed that tartaric acid was effective in removing the exchangeable, carbonate fractions of Cd, Zn and Cu from the contaminated soil. The contents of Pb and Cu in Fe-Mn oxide fraciton were also significantly decreased by tartaric acid treatment. One hundred milliliters of tartaric acid solution containing HMs could be regenerated by 10 g chestnut shells in a batch reactor. Such a remediation procedure indicated that tartaric acid is a promising agent for remediation of HM contaminated soils. However, further research is needed before the method can be practically used for in situ remediation of contaminated sites.