改性措施对复合污染土壤重金属行为影响的研究

采用田间实验的方法,研究了在复合污染土壤上石灰＋Ｃａ、Ｍｇ、Ｐ肥处理对重金属迁移、积累的影响及重金属的作物效应．结果表明,在污染土壤上采用石灰＋Ｃａ、Ｍｇ、Ｐ肥处理可减少重金属向作物籽实的迁移和积累,特别是Ｃｄ、Ｐｈ、Ａｓ３元素;改性以后,水稻、小麦Ｃｄ吸收量比改性前降低了３１．５—５５％．４种作物对Ｐｈ的吸收量降低了２３．４－５７．８％,Ｃｕ、Ｚｎ吸收量略有降低．水稻Ａｓ吸收量增加了５６．８％,小麦、大豆Ａｓ吸收量减少６１．８－８１．１％．重金属在土壤中存在的形态发生了变化,Ｃｄ、Ｐｈ、Ｚｎ交换态百分含量不同程度地有所减少,而碳酸盐结合态有所增加,可被植物吸收利用的有效含量降低．     

汞胁迫对植物细胞结构与功能的影响

由于工业“三废”和机动车尾气的大量排放、污水灌溉以及农药、除草剂和化肥的广泛使用,严重地污染了土壤、水质和大气,其中土壤中的重金属（Hg、Cd、As、Cu和Al）污染更为严重。这些重金属都会被生活在这种环境中的各种植物吸收。然后大量积累在它们的根、茎和叶中,对植物造成严重危害。     

桂北典型锰矿区周边土壤重金属污染状况及主要植物富集特征

为探究桂北某典型锰矿尾库区周边土壤和农作物重金属污染状况,筛选适合该地区污染土壤修复的植物材料,该研究在矿区周边采集了9种农作物和23种主要植物及其根际土壤,并测定了Cd、Mn、Cr、Pb和Zn 5种重金属含量,采用单因子污染指数法和综合污染指数法评价了矿区农田土壤、农作物中重金属的生态风险,通过计算植物对重金属的富集和转运系数评估其应用潜力。结果表明:(1)研究区土壤Cd、Mn污染最为严重,单因子污染指数分别为18.53、147.09,达到重度污染级别。(2)研究区花生和小白菜等作物可食用部位中的Cd、Cr、Pb含量均超过食品国家安全标准(GB 2762—2017)中的阈值,具有较高健康风险。(3)23种主要植物中青葙、鬼针草、一点红、蜈蚣草等对多种重金属转运系数大于1,具备富集型植物特征; 一把伞南星、蓖麻、千里光等根部重金属含量较高,转运系数较低,具备根部囤积型植物特征; 响铃豆、筒轴茅、苣荬菜等富集的重金属含量相对较低,且在重金属污染土壤中能健康生长,具备规避型植物特征。该研究结果表明,研究区土壤存在较严重的Cd/Mn复合污染,青葙等植物用于修复该复合污染土壤极具应用潜力。     

铜矿区超积累Cu植物的研究

1　引　　言土壤重金属污染一直是环境污染问题之一 ,而且土壤中的重金属污染具有严重性、长期性和广泛性的特点[1 ,6] .但常规的一些物理化学方法因费用过高、对土壤性质破坏等一系列问题而难以广泛应用 ,植物修复为重金属污染带来了希望[5,7,9,1 3] .植物修复主要是基于重金属超积累植物 (ｈｙｐｅｒ ａｃｃｕｍｕｌａｔｏｒ)的研究而兴起的 .超积累植物是指地上部分能富集重金属占干重的 1 0 0ｍｇ·ｋｇ-1 (Ｃｕ、Ｐｂ、Ｃｄ)或 1 0 0 0 0ｍｇ·ｋｇ-1 (如Ｚｎ)的一类植物[2～ 4,8] .在过去 2 0年内 ,已报道的超积累植物已有 4 0 0余种 …     

根际促生菌强化植物修复重金属污染土壤的研究进展

植物修复虽然是近年来土壤重金属污染修复的重要手段之一,但因修复植物生长缓慢、生物量小、重金属转移率低等因素严重影限制了植物修复技术的广泛应用。根际促生菌(plant growth promoting rhizobacteria,PGPR)作为一类生长在植物根际土壤中的微生物,不仅能够利用自身的抗性系统减缓重金属离子对植物的毒性,还能够改变重金属的形态和迁移率,并通过分泌铁载体、有机酸、生物表面活性剂、植物激素等作用,直接或者间接地促进植物生长和增强植物对重金属的抗性,在强化植物修复土壤重金属污染过程中发挥着重要的作用。现介绍了根际促生菌的种类及其重金属抗性机制,总结了近年来国内外关于根际促生菌促进植物生长、强化植物修复重金属污染土壤的作用原理,同时对该研究领域目前存在的问题以及今后的研究前景进行展望,以期为今后土壤重金属修复研究提供新的思路和理论依据。     

湖南柿竹园矿区土壤重金属含量及植物吸收特征

矿区重金属污染十分严重,寻找和发现适合当地气候与土壤条件的重金属耐性植物是矿区植被恢复和污染土壤修复的前提。对我国湖南柿竹园有色金属矿区调查发现,该地区选矿厂的重金属污染问题普遍比尾砂库严重。选矿厂土壤砷、镉、铅、锌严重超标,尾砂库周围也受到不同程度的重金属污染。土壤重金属胁迫效应影响着植物物种分布,选矿厂物种分布较少,相比之下尾砂库的植物多样性较为丰富。柿竹园矿区植物对重金属的吸收表现为富集型(如蜈蚣草Pteris Vittata L .和苎麻Boehmerianivea (L .) Gaud.)、根部囤积型(如攀倒甑Patrinia villosa和木贼Equisetum hyemale)和规避型(如蔓出卷柏Selaginelladavidii Franch和芒草Miscanthus sinensis Andlerss)等3种类型。     

植物修复——治理土壤重金属污染的新途径

介绍了重金属污染土壤的植物修复的概念、原理与研究动态以及重金属超积累植物的特性 ,及其在治理污染土壤中的潜力 ,为土壤重金属污染的整治及其生态的修复提出新途径。     

铅锌矿区土壤和植物重金属污染调查分析

对有色金属矿区土壤和植物重金属污染状况调查结果表明,由于遭受尾矿砂及矿毒水污染,矿区土壤极端贫瘠,土壤中Pb、Cd、Zn和Cu含量分别达764.74、4.10、372.75和95.57 mg.kg-1,重金属污染较为严重。在矿区周边有9种优势植物能够在污染土壤上定居,对Cu、Cd、Pb和Zn 4种重金属元素均有不同程度的积累,积累量均未达到超累积植物所规定的临界含量。其中的野菊花〔Dendranthema indicum(L.)Des Mou l.〕、旋鳞莎草〔Cyperusm ichelianus(L.)L ink〕、五节芒〔M iscanthus floridulus(Lab ill.)W arb.ex Schum.et Laut.〕3种植物地上部生物量较大且对某些重金属向地上部转运能力较强,对重金属污染土壤有一定的修复潜力。     

粤东铅锌尾矿三种优势植物对重金属的吸收和富集特性研究

为探讨铅锌矿废弃地优势植物在重金属污染土壤植物修复中的应用潜力,利用野外采样分析法,从粤东梅县丙村铅锌尾矿区采集其三种优势植物类芦、黄荆、盐肤木的根、茎、叶和土壤样品,测定和分析Pb、Zn、Cu、Cd四种重金属含量.结果表明:该矿区土壤污染严重,Pb、Zn、Cd含量远超土壤环境质量的三级标准,Cu超出二级标准;根际土壤和非根际土壤重金属含量均为Pb＞Zn＞Cu＞Cd,但根际土壤的重金属含量显著低于非根际土壤;这三种植物对Pb、Zn、Cu的转移系数大于1.0,对Cu的富集系数最高,Pb最小,但对四种重金属的富集系数均小于1.0,均未达到超富集植物临界含量标准.三种植物为该矿区的优势植物,说明它们对土壤的重金属污染有很强的耐性,虽然并非典型的超富集植物,但对污染土壤仍有较好的修复效果.     

溶磷微生物在钝化和植物修复重金属污染土壤中的作用

钝化和植物修复是重金属污染土壤修复的重要技术手段,而溶磷微生物可进一步增强钝化和植物修复重金属污染土壤的作用。介绍了钝化和植物修复重金属污染土壤的基本原理,总结了溶磷微生物对土壤中难溶性磷酸盐的溶解、利用磷酸盐钝化修复重金属污染土壤、溶磷微生物对磷酸盐钝化修复的强化以及溶磷微生物强化植物修复重金属污染土壤的研究进展,探讨了溶磷微生物对重金属的抗性及其溶磷机理、溶磷微生物对磷酸盐钝化修复重金属污染土壤的强化作用机理以及溶磷微生物强化植物修复重金属污染土壤的作用机理。旨在为生物修复重金属污染土壤研究提供一定的理论依据和技术支撑。     

Metal oxidoreduction by microbial cells

Summary For many organisms, some heavy metals in external media are essential at low concentrations but are toxic at high concentrations. Strongly toxic heavy metals are toxic even at low concentrations. Recently, it was proven that changes of valencies of Fe, Cu and Mn were necessary for these metals to be utilized by organisms, especially microorganisms. The valencies of Hg and Cr are changed by reducing systems of cells in the process of detoxifying them. Thus, the processes of oxidoreduction of these metals are important for biological systems of metal-autoregulation and metal-mediated regulation. Metal ion-specific reducing enzyme systems function in the cell surface layer of microorganisms. These enzymes require NADH or NADPH as an electron donor and FMN or FAD as an electron carrier component. Electron transport may be operated by transplamsa-membrane redox systems. Metal ion reductases are also found in the cytoplasm. The affinities of metal ions to ligand residues change with the valence of the metal elements and mutual interactions of various metal ions are important for regulation of oxidoreduction states. Microorganisms can utilize essential metal elements and detoxify excess metals by respective reducing enzyme systems and by regulating movement of heavy metal ions.     

Bacterial resistances to mercury and copper.

Heavy metals are toxic to living organisms. Some have no known beneficial biological function, while others have essential roles in physiological reactions. Mechanisms which deal with heavy metal stress must protect against the deleterious effects of heavy metals, yet avoid depleting the cell of a heavy metal which is also an essential nutrient. We describe the mechanisms of resistance in Escherichia coli to two different heavy metals, mercury and copper. Resistance of E. coli to mercury is reasonably well understood and is known to occur by transport of mercuric ions into the cytoplasmic compartment of the bacterial cell and subsequent reductive detoxification of mercuric ions. Recent mutational analysis has started to uncover the mechanistic detail of the mercuric ion transport processes, and has shown the essential nature of cysteine residues in transport of Hg(II). Resistance to copper is much less well understood, but is known to involve the increased export of copper from the bacterial cell and modification of the copper; the details of the process are still being elucidated. Expression of both metal resistance determinants is regulated by the corresponding cation. In each case the response enables the maintenance of cellular homeostasis for the metal. The conclusions drawn allow us to make testable predictions about the regulation of expression of resistance to other heavy metals.     

Biochemical changes and adaptive strategies of plants under heavy metal stress

Heavy metal contamination of soil, aqueous waste stream and ground water causes major environmental and human health problems. Heavy metals are major environmental pollutants when they are present in high concentration in soil and show potential toxic effects on growth and development in plants. Due to unabated, indiscriminate and uncontrolled discharge of hazardous chemicals including heavy metals into the environment, plant continuously have to face various environmental constraints. In plants, seed germination is the first exchange interface with the surrounding medium and has been considered as highly sensitive to environmental changes. One of the crucial events during seed germination entails mobilization of seed reserves which is indispensable for the growth of embryonic axis. But, metabolic alterations by heavy metal exposure are known to depress the mobilization and utilization of reserve food by affecting the activity of hydrolytic enzymes. Some plants possess a range of potential mechanisms that may be involved in the detoxification of heavy metals by which they manage to survive under metal stress. High tolerance to heavy metal toxicity could rely either on reduced uptake or increase planned internal sequestration which is manifested by an interaction between a genotype and its environment. Such mechanism involves the binding of heavy metals to cell wall, immobilization, exclusion of the plasma membrane, efflux of these toxic metal ions, reduction of heavy metal transport, compartmentalization and metal chelation by tonoplast located transporters and expression of more general stress response mechanisms such as stress proteins. It is important to understand the toxicity response of plant to heavy metals so that we can utilize appropriate plant species in the rehabilitation of contaminated areas. Therefore, in the present review attempts have been made to evaluate the effects of increasing level of heavy metal in soils on the key behavior of hydrolytic and nitrogen assimilation enzymes. Additionally, it also provides a broad overview of the strategies adopted by plants against heavy metal stress.     

植物重金属转运蛋白研究进展

土壤中的有毒重金属不仅对植物有害,也可通过食物链危害人类和动物的健康.重金属转运蛋白在植物吸收、抵抗重金属的复杂机制中起着关键作用.植物重金属转运蛋白分为吸收蛋白和排出蛋白,其中,吸收蛋白转运必需重金属进入细胞,同时也会因为必需重金属的缺乏或离子之间的竞争而运载有毒重金属;排出蛋白是一类解毒蛋白,可将过量的或有毒的重金属逆向转运出细胞,或区室化于液泡中.目前,细胞内多种重金属转运蛋白基因的转录水平与重金属离子积累之间的联系已被揭示,并分离克隆出诸多相关蛋白家族成员.本文综述了近年来发现并鉴定的主要重金属转运蛋白的金属亲和性、器官表达特异性及细胞内定位等的研究进展.     

Cellular mechanisms for heavy metal detoxification and tolerance.

Heavy metals such as Cu and Zn are essential for normal plant growth, although elevated concentrations of both essential and non-essential metals can result in growth inhibition and toxicity symptoms. Plants possess a range of potential cellular mechanisms that may be involved in the detoxification of heavy metals and thus tolerance to metal stress. These include roles for the following: for mycorrhiza and for binding to cell wall and extracellular exudates; for reduced uptake or efflux pumping of metals at the plasma membrane; for chelation of metals in the cytosol by peptides such as phytochelatins; for the repair of stress-damaged proteins; and for the compartmentation of metals in the vacuole by tonoplast-located transporters. This review provides a broad overview of the evidence for an involvement of each mechanism in heavy metal detoxification and tolerance.     

A novel heavy metal ATPase peptide from <Emphasis Type="Italic">Prosopis juliflora</Emphasis> is involved in metal uptake in yeast and tobacco

Heavy metal pollution of agricultural soils is one of the most severe ecological problems in the world. Prosopis juliflora, a phreatophytic tree species, grows well in heavy metal laden industrial sites and is known to accumulate heavy metals. Heavy Metal ATPases (HMAs) are ATP driven heavy metal pumps that translocate heavy metals across biological membranes thus helping the plant in heavy metal tolerance and phytoremediation. In the present study we have isolated and characterized a novel 28.9 kDa heavy metal ATPase peptide (PjHMT) from P. juliflora which shows high similarity to the C-terminal region of P_1B ATPase HMA1. It also shows the absence of the invariant signature sequence DKTGT, and the metal binding CPX motif but the presence of conserved regions like MVGEGINDAPAL (ATP binding consensus sequence), HEGGTLLVCLNS (metal binding domain) and MLTGD, GEGIND and HEGG motifs which play important roles in metal transport or ATP binding. PjHMT, was found to be upregulated under cadmium and zinc stress. Heterologous expression of PjHMT in yeast showed a higher accumulation and tolerance of heavy metals in yeast. Further, transgenic tobacco plants constitutively expressing PjHMT also showed increased accumulation and tolerance to cadmium. Thus, this study suggests that the transport peptide from P. juliflora may have an important role in Cd uptake and thus in phytoremediation.     

Microbial heavy-metal resistance

We are just beginning to understand the metabolism of heavy metals and to use their metabolic functions in biotechnology, although heavy metals comprise the major part of the elements in the periodic table. Because they can form complex compounds, some heavy metal ions are essential trace elements, but, essential or not, most heavy metals are toxic at higher concentrations. This review describes the workings of known metal-resistance systems in microorganisms. After an account of the basic principles of homoeostasis for all heavy-metal ions, the transport of the 17 most important (heavy metal) elements is compared. Received: 25 November 1998 / Received revision: 18 February 1999 / Accepted: 20 February 1999     

Plant responses to abiotic stresses: heavy metal-induced oxidative stress and protection by mycorrhization

The aim of this review is to assess the mode of action and role of antioxidants as protection from heavy metal stress in roots, mycorrhizal fungi and mycorrhizae. Based on their chemical and physical properties three different molecular mechanisms of heavy metal toxicity can be distinguished: (a) production of reactive oxygen species by autoxidation and Fenton reaction; this reaction is typical for transition metals such as iron or copper, (b) blocking of essential functional groups in biomolecules, this reaction has mainly been reported for non-redox-reactive heavy metals such as cadmium and mercury, (c) displacement of essential metal ions from biomolecules; the latter reaction occurs with different kinds of heavy metals. Transition metals cause oxidative injury in plant tissue, but a literature survey did not provide evidence that this stress could be alleviated by increased levels of antioxidative systems. The reason may be that transition metals initiate hydroxyl radical production, which can not be controlled by antioxidants. Exposure of plants to non-redox reactive metals also resulted in oxidative stress as indicated by lipid peroxidation, H(2)O(2) accumulation, and an oxidative burst. Cadmium and some other metals caused a transient depletion of GSH and an inhibition of antioxidative enzymes, especially of glutathione reductase. Assessment of antioxidative capacities by metabolic modelling suggested that the reported diminution of antioxidants was sufficient to cause H(2)O(2) accumulation. The depletion of GSH is apparently a critical step in cadmium sensitivity since plants with improved capacities for GSH synthesis displayed higher Cd tolerance. Available data suggest that cadmium, when not detoxified rapidly enough, may trigger, via the disturbance of the redox control of the cell, a sequence of reactions leading to growth inhibition, stimulation of secondary metabolism, lignification, and finally cell death. This view is in contrast to the idea that cadmium results in unspecific necrosis. Plants in certain mycorrhizal associations are less sensitive to cadmium stress than non-mycorrhizal plants. Data about antioxidative systems in mycorrhizal fungi in pure culture and in symbiosis are scarce. The present results indicate that mycorrhization stimulated the phenolic defence system in the Paxillus-Pinus mycorrhizal symbiosis. Cadmium-induced changes in mycorrhizal roots were absent or smaller than those in non-mycorrhizal roots. These observations suggest that although changes in rhizospheric conditions were perceived by the root part of the symbiosis, the typical Cd-induced stress responses of phenolics were buffered. It is not known whether mycorrhization protected roots from Cd-induced injury by preventing access of cadmium to sensitive extra- or intracellular sites, or by excreted or intrinsic metal-chelators, or by other defence systems. It is possible that mycorrhizal fungi provide protection via GSH since higher concentrations of this thiol were found in pure cultures of the fungi than in bare roots. The development of stress-tolerant plant-mycorrhizal associations may be a promising new strategy for phytoremediation and soil amelioration measures.     

The cell wall in plant cell response to trace metals: polysaccharide remodeling and its role in defense strategy

This review paper is focused predominantly on the role of the cell wall in the defense response of plants to trace metals. It is generally known that this compartment accumulates toxic divalent and trivalent metal cations both during their uptake by the cell from the environment and at the final stage of their sequestration from the protoplast. However, from results obtained in recent years, our understanding of the role played by the cell wall in plant defense response to toxic metals has markedly altered. It has been shown that this compartment may function not only as a sink for toxic trace metal accumulation, but that it is also actively modified under trace metal stress. These modifications lead to an increase in the capacity of the cell wall to accumulate trace metals and a decrease of its permeability for trace metal migration into the protoplast. One of the most striking alterations is the enhancement of the level of low-methylesterified pectins: the polysaccharides able to bind divalent and trivalent metal ions. This review paper will present the most recent results, especially those that are concerned with polysaccharide level, composition and distribution under trace metal stress, and describe in detail the polysaccharides responsible for metal binding and immobilization in different groups of plants (algae and higher plants). The review also contains information related to the entry pathways of trace metals into the cell wall and their detection methods.     

Antioxidant role of metallothioneins: a comparative overview.

Metallothioneins (MTs) are sulfhydryl-rich proteins binding essential and non-essential heavy metals. MTs display in vitro oxyradical scavenging capacity, suggesting that they may specifically neutralize hydroxyl radicals. Yet, this is probably an oversimplified view, as MTs represent a superfamily of widely differentiated metalloproteins. MT antioxidant properties mainly derive from sulfhydryl nucleophilicity, but also from metal complexation. Binding of transition metals displaying Fenton reactivity (Fe,Cu) can reduce oxidative stress, whereas their release exacerbates it. In vertebrates, MT gene promoters contain metal (MRE) and glucocorticoid response elements (GRE), Sp and AP sequences, but also antioxidant response elements (ARE). MT neosynthesis is induced by heavy metals, cytokines, hormones, but also by different oxidants and prooxidants. Accordingly, MT overexpression increases the resistance of tissues and cells to oxidative stress. As for invertebrates, data from the mussel show that MT can actually protect against oxidative stress, but is poorly inducible by oxidants. In yeast, there is a Cu(I)-MT that in contrast to mammalCu-MT exhibits antioxidant activity, possibly due to differences in metal binding domains. Finally, as the relevance of redox processes in cell signaling is becoming more and more evident, a search for MT effects on redox signaling could represent a turning point in the understanding of the functional role of these protein.