镉铅在粘土上的吸附及受腐殖酸的影响

试验研究了镉和铅2种重金属在蒙脱土和高岭土上的吸附,以及外加腐殖酸的3种组分（富里酸、棕色胡敏酸和灰色胡敏酸）的影响。镉铅在粘土上的吸附随着介质pH的升高而增加。在pH4-8范围内的任意pH点,镉在高岭土上的吸附量因富里酸而降低,因2种胡敏酸而升高;当pH值高于6时,吸附量急剧增加。外加富里酸使得铅在粘土上的吸附在pH＞6时意外出现随着介质pH而降低的趋势。     

Adsorption of chloroacetanilide herbicides on soil and its components Ⅲ. Influence of clay acidity, humic acid coating and herbicide structure on acetanilide herbicide adsorption on homoionic clays

Adsorption of chloroacetanilide herbicides on homoionic montmorillonite, soil humic acid, and their mixtures was studied by coupling batch equilibration and FT-IR analysis. Adsorption isotherms of acetochlor, alachlor, metolachlor and propachlor on Ca²⁺-, Mg²⁺ -. Al³⁺ -and Fe³⁺ -saturated clays were well described by the Freundlich equation. Regardless of the type of exchange cations, Kf decreased in the order of metolachlor ＞ acetolachlor ＞ alachlor ＞ propachlor on the same clay. FT-IR spectra showed that the carbonyl group of the herbicide molecule was involved in binding, probably via H-bond with water molecules in the clay interlayer. The type and position of substitutions around the carbonyl group may have affected the electronegativity of oxygen, thus influencing the relative adsorption of these herbicides. For the same herbicide, adsorption on clay increased in the order of Mg²⁺ ＜ Ca²⁺ ＜ Al³⁺ ≤ Fe³⁺ which coincided with the iucreasing aciditv of homoionic clays. Acidity of cations may have affected the protonation of water, and thus the strength of H-bond between the clay water and herbicide. Complexation of clay and humic acid resulted in less adsorption than that expected from independent adsorption by the individual constituents. The effect varied with herbicides, but the greatest decrease in adsorption occurred at a 60:40 clay-to-humic acid ratio for all the herbicides. Causes for the decreased adsorption need to be characterized to better understand adsorption mechanisms and predict adsorption from soil compositions.     

14C-甲磺隆在土壤中的可提态残留、结合态残留和矿化

在实验室培养条件下,从质量平衡角度,研究了14C-甲磺隆在7种土壤中形成结合残留(14C-BR)、可提态残留(14C-ER)以及矿化为14CO2的规律;同时对14C-BR的主要影响因子及其在腐殖质中的分布规律进行了研究.结果表明:①14C-甲磺隆在土壤中形成的14C-ER,其含量与土壤pH呈显著正相关.甲磺隆母体化合物在7种土壤中 的半减期为13.3～66.6d,降解速率常数λ(d-1)与pH呈显著负相关.②14C-甲磺隆在7种土壤中形成的14C-BR,其含量在培养初期的20d内,与土壤pH呈显著负相关且与土壤粘粒含量呈显著正相关;而培养20d后,14C-BR的含量只与土壤pH呈显著负相关.pH是04C-甲磺隆在土壤中形成BR的主要影响因子.14C-甲磺隆在7种土壤中的14C-BR的最大值约为引入量的19.3%～52.6%.③在整个培养试验过程中,7种土壤中的14C-BR主要分布在富啡酸和胡敏素中,但其分布在胡敏酸中的相对百分比较小.因此,在14C-甲磺隆形成BR的过程中,富啡酸的作用＞胡敏素>胡敏酸.④在整个培养试验期间(180d),14C-甲磺隆在7种土壤中通过三嗪杂环开环矿化为14CO2的量约占引入量的12.9%～27.0%,其在碱性土壤中更难被矿化为14CO2.     

Speciation and fractionation of heavy metals in soil experimentally contaminated with Pb,Cd, Cu and Zn together and effects on soil negative surface charge

Speciation and fractionation of heavy metals in soil subsamples experimentally loaded with Pb, Cd, Cu and Zn in orthogonal design was investigated by sequential extraction, and operationally defined as water-soluble and exchangeable(SE), weakly specific adsorbed( WSA),Fe and Mn oxides-bound(OX) and organic-bound( ORG). The results showed that fractions of heavy metals in the soil subsamples depended on their speciation. About 90% of Cd and 75% of Zn existed in soil subsamples in the SE fraction. Lead and Cu existed in soil subsamples as SE, WSA and OX fractions simultaneously, although SE was still the major fraction. Organic-bound heavy metals were not clearly apparent in all the soil subsamples. The concentration of some heavy metal fractions in soil subsamples showed the good correlation with ionic impulsion of soil, especially for the SE fraction. Continuous saturation of soil subsamples with 0.20 mol/L NH4CI, which is the first step for determination of the negative surface charge of soil by the ion retention method, resulted in desorption of certain heavy metals from the soil. It was found that the percentage desorption of heavy metals from soil subsamples depended greatly on pH, the composition and original heavy metal content of the soil subsamples. However, most of the heavy metals in the soil subsamples were still be retained after multiple saturation. Compared with the parent soil, the negative surface charge of soil subsamples loaded with heavy metals did not show difference significantly from that of the parent one by statistical analysis. Heavy metals existed in the soil subsamples mainly as exchangeable and precipitated simultaneously.     

农田土壤中的磷向水体释放的风险评价

通过对比土壤的固磷能力和磷素水平可以评估不同类型土壤中的磷向水体释放的风险。研究表明，磷吸持指数（SI）可以作为土壤最大吸磷量的替代指标来表征土壤的固磷能力。在太湖地区，影响水土界面磷素迁移能力的主要因素是土壤有效磷水平和土壤固磷能力。SI值30左右为一临界值，SI大于此值的土壤对于施磷具有较大的缓冲能力，而SI低于此值的土壤对施磷非常敏感，磷流失风险将随施磷量的增加而呈直线上升趋势。     

沂北水稻主产区田间土—水磷素流失潜能

选取嘉善、余姚、德清、余杭4个具有代表性浙北水稻主产区，研究了水田土－水磷素流失潜能及环境意义。4稻区高水平磷肥投入促进了土壤高磷化，土壤Olsen-P积累的同时,相应地提高了土壤生物性有效磷、水浸提磷，并提高了土壤磷素的流失潜能。稻区土壤在富磷化过程中，存在着土壤磷素的农学意义向环境意义方向演变的趋势。在非植稻期，稻区农田水体，包括沟渠水、田表水、排渠水、暗管排水等总磷（TP）平均超过了易诱发水体富营养化临界值，其中溶解磷（DRP）占总磷40％；主要是源于绿肥田表水及部分排渠中的溶解磷对稻区外水体构成了直接危害。在非植稻期，因稻区间农耕措施的差异导致了土壤富磷水平与对应田表水磷素水平不具相关性；在植稻期，施磷措施促进水田土壤富磷，相应地提高了田表水磷素水平。     

土壤重金属污染对蚯蚓（Opisthopora）影响的研究

研究了重金属污染区蚯蚓的群落结构、污染指示种类、以及污染影响的毒理指标．结果表明：随着重金属污染程度的增加，蚯蚓种类减少，蚯蚓体内重金属元素富集量增加．蚯蚓毒理实验表明：Ｃｄ中毒后过氧化物同工酶活性增加，脂酶同工酶活性减弱．Ｐｂ中毒后蚯蚓过氧化物酶和脂酶同工酶活性均增加．     

甘肃省环境天然放射性水平研究

近年来,国内外在环境天然放射性水平研究方面做了一些工作.在国内,由于研究目的各有侧重,因而在布点原则等方面有所不同.在全国环境保护系统的天然放射性水平研究中,象甘肃省这种跨度大(东经92°13′—108°46′,北纬32°31′—42°57′)、地形地貌极其复杂(有沙漠、戈壁、山区、高原、草原、河谷盆地等)、海拔高度差别悬殊(有600m河     

海河流域硫的区域库存量与流通量研究

本文通过对海河流域土壤中硫及其形态含量的分析结果，计算出该流域土壤中硫的库存量为７．９０×１０＾ｋｇ。并以径流带入量，成土母质，人畜粪，化肥施入量，大气降尘及植物的残留量等因素为对土壤中硫的贡献；同时，以径流的带出，大气的扬尘量及植物体茎，叶因素为硫的迁出部分，以计算出海河流域土体中硫的进出量为０．６８×１０＾９ｋｇ／ｙｒ，１．７１×１０＾９ｋｇ／ｙｒ，以此来研究其流通关系。