回归模型法推导油菜田土壤Cd限值的不确定性

为研究土壤-作物迁移模型推导农田土壤环境基准的不确定性,以油菜为例,通过贵州省4种典型微酸性土壤——红壤、黄壤、石灰土和黄棕壤进行Cd盐添加的盆栽试验,除全量Cd外,选择5种有效态提取剂,分别与油菜籽w(Cd)建立土壤-作物迁移模型. 参照GB 13078—2001《饲料卫生标准》w(Cd)限值(0.5 mg/kg),采用模型预测中位值和95%预测上限进行土壤Cd限值推导并分析模型的不确定性. 结果表明:全量和各提取态Cd质量分数与油菜籽w(Cd)均能建立极显著的一元(R2为0.907~0.946)或多元(考虑pH)回归模型(R2为0.875~0.962). 5.550(以多元模型中位值推导的农田安全种植油菜的Cd限值)随pH的升高从0.93 mg/kg增至1.45 mg/kg,HNO₃提取态、HCl提取态、DTPA提取态的Cd的质量分数也分别从0.81、0.97、0.73 mg/kg升至1.39、1.79、1.66 mg/kg. 基于CaCl₂提取态Cd的一元模型对pH不敏感,SEQS₅₀不受其影响. 对所有模型而言,SEQS₅₀是SEQS₉₅(基于模型95%的预测上限推导的限值)的1.1倍左右. 其中,CaCl₂提取态Cd的SEQS₅₀和SEQS₉₅分别为0.052和0.049 mg/kg,小于福建省CaCl₂提取态Cd标准限值(0.15 mg/kg). 为降低不确定性,需要选择合适的提取剂,使用全量Cd,HNO₃、HCl或DTPA 3种提取态Cd建模时须兼顾pH的影响. 研究显示,SEQS₉₅能够降低土壤Cd限值达标而作物Cd含量超标的可能性.      

热解制备玉米秸秆和城市污泥生物炭过程中PAHs的污染特征

以玉米秸秆和城市污泥为生物质原材料,并于300、500、700 ℃下厌氧热解,分析生物炭和生物油中PAHs的生成、分配及毒性特征.结果表明:玉米秸秆和城市污泥在300～700 ℃下热解后分配于生物炭中的w(PAHs)分别为116.8～1 807和136.3～52 015 μg/kg,分配于生物油中的w(PAHs)分别为10 612～33 402和11 077～116 673 μg/kg.生物炭和生物油中以低环PAHs(2环～4环)为主,其所占比例分别为90.8%～99.6%和97.9%～99.5%.大部分PAHs分配于生物油相,生物炭中PAHs的残留量较小,其中,5环PAHs是生物炭和生物油中苯并芘毒性当量浓度(TEQ_BaP)的主要贡献者.      

太湖重金属和营养盐污染特征分析

对太湖各湖区采样点沉积物的重金属Zn、Cu、Mn、Cr、Pb及营养盐Fe-P、TP含量进行分析.结果表明,太湖重金属含量高于地壳中的背景值,Cr和Pb富集程度高于其他金属.几乎所有采样点的沉积剖面的Pb含量自底部向表层迅速增加,表明1950年以来太湖流域含Pb等污染物的工业废水大量排放.竺山湾的重金属及营养盐的污染程度...     

农田排水中磷素对苏南太湖水系的污染

采用封闭体系和磷素平衡方法研究苏南太湖地区农业面源中磷的排出负荷量和减少排出负荷量的措施。实验结果表明,雨水较丰富的１９８７年,苏南太湖流域农田地表排出磷的总负荷量为４４０．４ｔ／ａ,而较为干旱的１９８８年为２９９．９ｔ／ａ。     

东太湖沉积物中氮的积累与水生植物沉积

为揭示浅水湖泊沉积物中氮的积累及其与水生植物间的关系,1993年11月在东太湖42个样点上采集了沉积物柱状样品并进行了分析。东太湖硬度小于5kgf/cm²的松软淤积层平均厚度0.96m,全湖淤积量149×106t。粉沙质淤积物中总氮（TN）含量0.009％～0.801％,总有机碳（TOC）含量0.01％～17.36％,变幅极为悬殊。总氮含量与总有机碳含量间呈密切的线性正相关TN（％）＝0.0251TOC（％）＋0.0063,表层沉积物中总氮和总有机碳含量都与水生植物的现存量有较为显著的正相关。这说明,氮和有机碳主要经过水生植物的生物沉积途径进入沉积物,水生植物有将湖水中的氮传输到底泥中,使其进入地球化学循环的功能,这对于降低湖水中的氮含量、防止富营养化有积极的意义     

Case study on nitrogen and phosphorus emissions from paddy field in Taihu region

The agricultural non-point source pollution by nitrogen (N) and phosphorus (P) loss from typical paddy soil (whitish soil, Bai Tu in Chinese) in the Taihu Lake region was investigated through a case study. Results shown that the net load of nutrients from white soil is 34.1 kg ha(-1) for total nitrogen (TN), distributed as 19.4 kg ha(-1), in the rice season and 14.7 kg ha(-1) in the wheat season, and for total phosphorus (TP) 1.75 kg ha(-1), distributed as 1.16 kg ha(-1) in the rice season and 0.58 kg ha(-1) in the wheat season. The major chemical species of N loss is different in the two seasons. NH4-N is main the form in the rice season (53% of TN). NO3-N is the main form in wheat season (46% of TN). Particle-P is the main form in both seasons, (about 56% of TP). The nutrient loss varied with time of the year. The main loss of nutrients happened in the 10 days after planting, 64% of TN and 42% of TP loss, respectively. Rainfall and fertilizer application are the key factors which influence nitrogen and phosphorus loss from arable land, especially rainfall events shortly after fertilizer application. So it is very important to improve the field management of the nutrients and water during the early days of planting.     

长江中下游浅水湖泊沉积物中磷的形态及其与水相磷的关系

研究了长江中下游22个不同生态类型的浅水湖泊表层沉积物中磷的地球化学形态及水相磷含量等水质特征.对沉积物中磷形态的连续提取分析发现,自然粒度下,绝大部分湖泊的沉积物中90%以上的磷是以生物较难利用的形态存在的,活性磷所占比例很小.而在严重污染的城市湖泊中,活性磷含量则可以占到总磷的35%以上.沉积物中活性磷含量的高低与总磷含量并不一致.水草的存在对水相磷含量及沉积物中磷的活性都有显著的影响.水相磷的含量与沉积物中交换态磷的含量、沉积物铁磷比有显著的相关关系.研究表明,沉积物地球化学性质、水体营养盐含量及浅水湖泊生态类型之间存在复杂而密切的联系.     

滇池水体和沉积物中营养盐的分布特征

在滇池外海不同方位选取6个采样点,研究了水质现状,沉积物Eh,pH,总氮,总磷以及间隙水重金属的剖面分布特征。结果表明,滇池水体仍属富营养化状态。在氧化表层下,Eh随沉积深度的增加迅速降低,沉积物深层为还原状态。pH在沉积物剖面变化不大,为7 0～8 5。滇池沉积物含有丰富的营养物质,总氮和总磷最高质量分数分别为8 67和3 46g kg。剖面分布表明,沉积物表层总氮和总磷含量远高于底层,在表层0～10cm含量随深度增加而迅速降低。重金属元素在水-土界面的浓度梯度为沉积物向水体的扩散提供了条件。不同采样点相比,位于昆明市附近的S6点沉积物内负荷较大。在外源减少的情况下,沉积物内负荷可能在一定时间内成为控制滇池水质的主导因子。      

小型湖泊修复区与未修复区对生态修复的响应与评价

为研究湖泊生态修复后小型城市湖泊不同区域水生态状况的长期响应特征,并探讨利用不同水生生物类群评价水体水生态状况的适用性,于2018年1月～2019年5月,对湖南小型城市湖泊松雅湖水质及不同水生生物类群分别进行了逐月和季度监测,并对其水生态状况进行了评价.结果显示,与生态修复之前相比,修复后松雅湖全湖相关水质指标均优于修...     

Electrokinetic removal of chromium and copper from contaminated soils by lactic acid enhancement in the catholyte

The electrokinetic removal of chromium and copper from contaminated soils by adding lactic acid in cathode chamber as an enhancing reagent was evaluated. Two sets of duplicate experiments with chromium contaminated kaolinite and with a silty soil sampled from a supeffund site in Califomia of USA and polluted by Cr and Cu, were carried out in a constant current mode. Changes of soil water content and soil pH before and after the electrokinetic experiments, and variations of voltage drop and electroosmosis flow during the treatments were examined. The results indicated that Cr, spiked as Cr(Ⅵ) in the kaolinite, was accumulated mainly in the anode chamber, and some of Cr and metal hydroxides precipitated in the soil sections in contact with the cathode, which significantly increased electrical energy consumption. Treatment of the soil collected from the site showed accumulation of large amounts of Cr and Cu in the anode chamber while none was detected in the cathode one. The results suggested that the two metals either complexed with the injected lactic acid at the cathode or existed as negatively charged complex, and electromigrated toward the anode under a voltage gradient.