土壤中氧化铁的有机还原溶解动力学

研究了土壤中的氧化铁被两种酚化合物还原而溶解的动力学，结果表明，在ｐＨ恒定和有机还原剂过量的情况下，氧化铁的还原溶解符合一级反应动力学方程，还原溶解速率大小与土壤中氧化铁的结晶形态有关．氧化锰的存在影响着氧化铁的还原溶解，在存在足够的还原剂的条件下，两者可同时还原．实验中求得黄壤和赤红壤中氧化铁的还原溶解反应对［Ｈ＋］的反应级数分别为０．１２６和０．１７４。土壤中氧化铁的还原溶解是一个受表面反应控制的过程，反应的速率控制步骤是表面的电子转移反应，磷酸根在土壤中的吸附占据了氧化铁表面的反应位，因而明显抑制还原溶解反应．     

广州市蔬菜地重金属剂量对蔬菜富集重金属的影响--以菜心为例

调查并分析了广州市蔬菜地土壤和菜心中主要重金属元素质量分数，通过多元统计分析建立了菜心中某一重金属元素和土壤中元素的数学回归模型。结果表明，Cd更易在菜心体内造成累积；总体上菜心中重金属质量分数与其在土壤中的质量分数有一定的相关性，菜心中Pb、As的积累分别取决于土壤中Pb、As的质量分数，土壤中Pb和As还分别促进了菜心对Cr、Hg的吸收，Pb对菜心中Cd的累积表现为协同作用；土壤重金属质量分数临界值可为今后无污染蔬菜的生产提供参考依据。     

Dissolved Organic Matter in Forest Soils: Sources, Complexing Properties and Action On Herbaceous Plants

Dissolved organic matter (DOM) is an important component of plant-soil systems. Its essential role in soil solution chemistry, soil-forming processes and its effects on biota, including soil fauna, bacteria, fungi and plants, is extensively documented in literature. in this contribution several forest leaf litter types are compared as sources of DOM and the released organics are subjected to gel permeation chromatography to reveal their molecular-size distribution. Moreover, complexing properties, as an indication for the podzolization potential of the litter leachates, were established. the occurrence and properties of DOM in different soil horizons were monitored beneath a stand of Scots pine. the effects of the different groups of soluble organics including phenolic, fulvic and humic acids, and of water-extractable humic substances on the performance of herbaceous plants of the forest floor are briefly reviewed.     

有机氯农药六六六污染土壤的植物修复研究

我国20世纪六七十年代大量施用的有机氯农药,由于其性质极其稳定,在土壤至今仍有残留。植物修复有机农药污染土壤并不多见,但具有广阔的应用前景。此项研究对提高土壤环境质量、保证农产品的安全、实现农业可持续发展等有着重要的理论和现实意义。文章以多花黑麦草(Lolium multiforum Lan.)、紫花苜蓿(Medicago sativa L.)和籽粒苋(Amaranthus hypochondriacus L.)作为供试植物,在有机氯农药六六六(HCH)质量分数为1.09 mg.kg-1的污染土壤中种植3个月,研究了种植不同植物条件下土壤中HCH的消解情况。研究结果表明,与对照相比,种植植物大大提高了土壤中微生物数量和酶的活性,并且微生物的数量和酶的活性与土壤中HCH的消解密切相关。试验结束后,不同处理中HCH及其4种异构体的总含量降低幅度为43.87%~65.79%,其中种植紫花苜蓿和多花黑麦草的处理中HCH消解较快,对HCH污染土壤修复的效果较好。可见,植物修复技术是一种可行的环境友好的修复六六六污染土壤的技术。     

稻田土壤对铵的矿物固定对土壤保氮作用的贡献

为了定量评价土壤对铵的矿物固定作用在土壤对肥料氮的保持作用中的相对贡献,通过室内培养试验和分析测定,研究了湖南省几种主要母质发育的水稻土对添加铵的矿物固定作用及其对土壤保氮作用的贡献。结果表明:土壤对外源铵的矿物固定是土壤重要的保氮机制之一,但不同土壤对保氮作用的相对贡献大小不一,以河沙泥的固铵作用对土壤保氮作用的贡献最大,固铵量占总保氮量的51.5%,红黄泥最低,固铵量仅占总保氮量的17.1%,其余五种土壤的固铵作用对土壤保氮作用的贡献大小顺序依次是黄泥田(43.7%)、湖潮泥(35.5%)、紫泥田(35.4%)、灰泥田(25.0%)、麻沙泥(20.8%)。     

模拟酸雨对红壤铝形态的影响

用动态淋洗试验，研究了不同pH的模拟酸雨对红壤中铝形态和性质的影响．结果表明，酸雨淋洗引起红壤中盐基离子的淋失和土壤铝的溶出．随着酸雨溶液pH的降低，盐基淋矢量和铝溶出量增加．酸雨淋洗影响土壤铝形态的转化，使红壤中交换态铝上升，吸附态羟基铝有所下降．这说明在酸雨长期作用下，羟基铝溶解，并转化为交换态铝和引起铝的溶出，使铝进入环境，危害生态系统．     

Geochemical evidence of pollutants from coalfired generating stations in late Pleistocene palaeosols in the Dalijia Shan,northwestern China

Surface palaeosols in two tills and a diamicton from an area in northwestern China were analysed for geochemical pollutants. Elevated levels of Br, As and Sb indicate that pollution from coal-burning and/or coal-fired electricity generating stations is delivered by aeolian transport into palaeosols dating from the last glaciation. Because the climate in the field area is sub-humid (precipitation <760 mm) the relative movement of soluble elements in palaeosols dating from early and late stades of the last glaciation is not expected to be high. The glacial and aeolian parent materials of the palaeosols indicate differences that are probably related to their source areas and to the incorporation of geochemical pollutants.     

铜陵矿区土壤中镉存在形态及生物有效性

采取Tessier连续提取法，研究铜陵矿区不同功能区表层土壤中镉的化学形态分布和生物有效性。结果表明，各种土壤中的镉含量全部高于地区背景值，主要来源与矿业活动有关，部分样品还有矿体的风化富集叠加，土壤镉污染指数PCd为1．15～79。镉含量依次为矿体风化土壤→废矿堆下垫土→市郊菜地土→矿区铜草土、路边土和稻田土→其它土壤。其形态分布，酸性土壤中以Fe-Mn氧化态和可交换态为主，其余三态相对较低；碱性土壤中有机态和残渣态比例较高，碳酸盐态和可交换态所占的比例低。土壤中生物可利用态镉的含量较高，占土壤总镉的60．20%-98．3％，生物不可利用态仅占1．7％-39．2％。     

表面活性剂对可离子化有机化合物在黄土中吸附行为的影响

研究了2，4-二氯苯酚、2，4-二硝基苯酚和苯甲酸三种可离子化有机化合物在天然黄土和阳离子表面活性剂改性黄土中的吸附行为。讨论了DH值、离子强度和二价重金属阳离子对可离子化有机化合物在改性黄土中吸附的影响。提出了可离子化有机化合物在改性黄土中的吸附模型，吸附等温曲线可分解为两条分别代表离子和非离子形态的等温吸附曲线；其吸附行为可用双模式吸附理论来解释。在2，4-二硝基苯酚共存时，苯甲酸在改性黄土中的吸附量减小，证明竞争吸附的存在。     

Reconnaissance soil geochemical survey of Gibraltar

The extreme density of population of Gibraltar, situated at the southern tip of Spain, exerts considerable pressure on land use and thus future planning is of utmost importance. An initial reconnaissance soil geochemical survey of Gibraltar was based on 120 surface samples (0–15 cm) taken from a wide range of exposed, either bare soil or vegetated sites, to provide the optimum geographical distribution. The total elemental concentrations of 26 elements (Li, Na, K, Be, Mg, Ca, Sr, Ba, Al, La, Ti, V, Cr, Mo, Mn, Fe, Co, Ni, Cu, Ag, Zn, Cd, Pb, P, S, As) were determined by nitric/percholric acid digestion followed by inductively coupled plasma-atomic emission spectrometry (ICP-AES) analysis. The reconnaissance data shows that the spatial distribution of various elements depended on previous and present land use. Most elements (Ca, Cr, Mg and Mn excluded) exhibited relatively high concentrations in civilian and natural soils. Trends have been established for many elements, and concentrations exceeding guideline values have been found in certain areas of Gibraltar. This reconnaissance of Gibraltar is at present being followed by a more detailed baseline geochemical survey, which will establish the extent and magnitude of the variations in major and trace elements in soils and dusts, assess the impact of industrial, commercial and urban development on the geochemical landscape and to make recommendations concerning sustainable development.