Phytoremediation of Cd,Ni, Pb and Zn by Salvinia minima

Most metals disperse easily in environments and can be bioconcentrated in tissues of many organisms causing risks to the health and stability of aquatic ecosystems even at low concentrations. The use of plants to phytoremediation has been evaluated to mitigate the environmental contamination by metals since they have large capacity to adsorb or accumulate these elements. In this study we evaluate Salvinia minima growth and its ability to accumulate metals. The plants were cultivated for about 60 days in different concentrations of Cd, Ni, Pb and Zn (tested alone) in controlled environmental conditions and availability of nutrients. The results indicated that S. minima was able to grow in low concentrations of selected metals (0.03 mg L^?1 Cd, 0.40 mg L^?1 Ni, 1.00 mg L^?1 Pb and 1.00 mg L^?1 Zn) and still able to adsorb or accumulate metals in their tissues when cultivated in higher concentrations of selected metals without necessarily grow. The maximum values of removal metal rates (mg m² day^?1) for each metal (Cd = 0.0045, Ni = 0.0595, Pb = 0.1423 e Zn = 0.4046) are listed. We concluded that S. minima may be used as an additional tool for metals removal from effluent.     

Structural comparison of alkylated derivatives of (bmmp-dmed)Ni and (bmmp-dmed)Zn

The sulfur-alkylation of the nickel (1) and zinc (2) complexes of the dithiolate N₂S₂ ligand N,N′-bis-2-methyl-mercaptopropyl-N,N′-dimethylethylenediamine, H₂(bmmp-dmed), have been investigated. Reactions with iodomethane yield [(Me-bmmp-dmed)Ni]PF₆ (3), [(Me₂-bmmp-dmed)NiI₂] (4), and [(Me₂-bmmp-dmed)ZnI]₂[ZnI₄] (5). Addition of iodoacetamide yields [(AA₂-bmmp-dmed)Ni]I₂ (6) and [(AA₂-bmmp-dmed)Zn]I₂ (7). Each of the metal-thioether products (3-7) have been characterized spectroscopically and by X-ray crystallography. Structural data is compared with that of the previously reported thiolato precursors 1 and 2. Sulfur-alkylation of 1 results in small relative changes in the nickel-sulfur bond distance, whereas for 2, the zinc-sulfur bond distance increases significantly, but is not cleaved. The difference between nickel and zinc is attributed to the release of a π*-bonding interaction between the metal and sulfur upon alkylation that compensates for the decreased σ-donor ability of the thioether in the case of nickel, but not for zinc.     

Synthesis, characterization and biological activity of Ni, Cu and Zn complexes of isatin hydrazones

Nickel, copper, and zinc complexes of isatin (H(2)L(1)) and N-methylisatin 3-picolinoyl hydrazone (HL(2)), were synthesized and characterized by means of spectroscopic techniques. H(2)L(1) and a nickel complex [Ni(L(2))(2)].2C(6)H(14) were also characterized by X-ray diffractometry. Biological studies, carried out in vitro on human leukemic cell lines TOM 1 and NB4, have shown that both ligands and some copper and nickel complexes are active in inhibiting cell proliferation. Compounds H(2)L(1), Cu(HL(1))(2).2H(2)O, Zn(HL(1))(2).2H(2)O inhibit DNA synthesis and act constantly with time between 0 and 72 h. The cell cycle analysis has highlighted a reduction in the number of cells in phase S of about 40%. The same compounds present only a precocious action on cell line NB4 and therefore their activity is cell target specific.     

模拟氮沉降对中亚热带森林土壤Ni、Cu、Zn含量的影响

通过野外模拟实验,研究3个氮沉降水平,CK(对照,0 kg·hm^-2·a^-1)、LN(低氮,30 kg·hm^-2·a^-1)和HN(高氮,100 kg·hm^-2·a^-1)处理对亚热带针叶(杉木)和阔叶(罗浮栲、浙江桂)森林土壤中微量元素Ni、Cu、Zn含量的影响。结果表明:就不同的林分来看,3种微量元素的含量大致呈杉木林>罗浮栲林>浙江桂林,施氮3 d后,浙江桂林和罗浮栲林土壤中3种微量元素在各处理之间差异不显著,仅发现杉木林土壤中的Ni含量在CK处理与LN及HN处理之间和无凋落物土壤中Cu含量在HN与CK及LN之间的差异显著; 3片林分中土壤表面有无凋落物处理总体对3种微量元素含量的影响不大。与施氮前相比,3片林分土壤中的Ni、Cu、Zn含量均有所下降,且浙江桂林在LN处理的降幅最大。     

Metal complexes increase uptake of Zn and Cu by plants: implications for uptake and deficiency studies in chelator-buffered solutions

The allocation of resources among roots and shoots represents the largest flux of resources within a plant and therefore should have been selected to maximize benefits to plants. Yet, it is unclear why some species like temperate grasses have such high root length density (RLD). Either the slow rate of diffusion of inorganic N in soils or interplant competition could explain the high RLD of temperate grasses. Using a fine-scale model of nutrient dynamics in the soil and plant growth, a cost–benefit approach was used to assess optimal allocation rates for plants that accounted for value of both carbon and nitrogen. In the absence of interplant competition, resource benefits are maximized with very little root length except in extremely dry soils for ammonium. In the presence of a competitor, optimal allocation of N to roots is much greater and increases as ability of competitors to produce root length increase. Competition for inorganic nitrogen generates a classic aspect of the tragedy of the commons, the “race for fish”, where plants must allocate more resources to acquisition of the limiting resource than is optimal for plants in the absence of competition. As such, nutrient competition needs to be directly addressed when understanding plant- and ecosystem-level resource fluxes as well as the evolution of root systems.     

Intrachloroplast Localization of 65Zn and 63Ni in a Zn-tolerant Plant, Ocimum basilicum Benth

Intrachloroplast localization studies of ⁶⁵Zn and ⁶³Ni weremade in a Zn-tolerant plant Ocimum basilicum var. purpurascensBenth. in order to investigate the mechanism and specificityof metal tolerance. The isotopes were supplied in solution tothe roots 14 d before fractionation. It was observed that ⁶⁵Znactivity was comparatively greater in the chloroplast envelopemembranes and stroma than the ⁶³Ni; and ⁶³Ni was largely foundin the lamellar and stroma fractions. Further analysis of lamellaerevealed that photosystem II (PS II) particles were richer inradioactivity than photosystem I (PS I) particles. The photochemicalevents of photosynthesis were less affected in Zn-treated plantsthan in the Ni-treated plants. The changed levels of the electrontransport chain intermediates including cytochromes, plastocyaninand ferredoxin provide supporting evidence for the localizationstudies. The activity of carbonic anhydrase, a zinc metalloprotein,was increased in Zn-treated plants with increase in nutrientZn concentration, indicating the binding of zinc to a proteinmoiety in the chloroplasts.     

Opportunities and feasibilities for biotechnological improvement of Zn, Cd or Ni tolerance and accumulation in plants

Metals contaminate the soil when present in high concentrations causing soil and ultimately environmental pollution. “Phytoremediation” is the use of plants to remove pollutants from contaminated environments. Plants tightly regulate their internal metal concentrations in a process called “metal homeostasis”. Some species have evolved extreme tolerance and accumulation of Zn, Cd and Ni as a way to adapt to exposure to these metals. Such traits are beneficial for phytoremediation, however, most natural metal hyperaccumulator species are not adapted to agriculture and have low yields. A wealth of knowledge has been generated regarding metal homeostasis in plants, including hyperaccumulators, which can be used in phytoremediation of Zn, Cd and Ni. In this review, we describe the current state of Zn, Cd and Ni physiology in plants and the underlying molecular mechanisms. The ways to efficiently utilize this information in designing high biomass metal accumulator plants are discussed. The potential and application of genetic modification has extended our understanding about the mechanisms in plants dealing with the metal environment and has paved the way to achieve the goal of understanding metal physiology and to apply the knowledge for the containment and clean up of metal contaminated soils.     

绿洲土Cd、Pb、Zn、Ni复合污染下重金属的形态特征和生物有效性

通过模拟基于干旱区绿洲土壤Cd-Pb-Zn-Ni复合污染下的油菜盆栽试验,采用Tessier五步连续浸提法探究了重金属复合污染对油菜生长的影响及其各形态的转化归趋和生物有效性.结果显示,随着Cd-Pb-Zn-Ni复合胁迫水平的升高,油菜的干重先增加后减小,根系的生长由促进作用转变为抑制作用;对照土壤中4种重金属元素均以残渣态为主要赋存形态,可交换态的含量均很小;随着外源重金属的添加,油菜种植土壤中4种重金属元素的各形态含量随之增加,Cd、Pb、Zn的可交换态和Ni的碳酸盐结合态对外界胁迫响应强度最大,Cd、Pb、Zn、Ni的活性增加,且Cd、Pb的主要赋存形态迅速转变为碳酸盐结合态和铁锰氧化态,Zn的主要赋存形态由残渣态和碳酸盐结合态过渡到碳酸盐结合态和铁锰氧化态,Ni的主要赋存形态为碳酸盐结合态;Cd、Zn在茎叶中的含量大于根系,Pb、Ni反之,油菜能将Cd、Zn更多的运输至茎叶,Pb、Ni则主要积累在根系;油菜茎叶吸收Cd和油菜各部位吸收Zn的主要贡献形态为可交换态,根吸收Cd的主要贡献形态由可交换态转变为有机结合态,根吸收Pb和油菜各部位吸收Ni的主要贡献形态为碳酸盐结合态.     

二球悬铃木不同器官对空气中Cu、Ni、Pb和Zn的累积作用

以交通繁忙区(污染点)和相对清洁区(对照点)道路两侧的二球悬铃木〔Platanus acerifolia ( Ait.) Willd.〕为研究对象,测定了不同器官(包括主干、老树皮、2年生枝条、1年生枝条、腋芽、叶片和果实)中Cu、Ni、Pb和Zn的含量,并对污染点二球悬铃木各器官中4种重金属元素的累积量和污染指数及二者的分布比例进行分析。结果表明：二球悬铃木体内重金属元素的含量因样点、器官及元素的不同而呈现不同的变化规律,污染点4种重金属元素的累积量及其分布比例、污染指数及其分布比例则因器官和元素的不同而有明显差异。总体上看,污染点各器官的Cu、Ni、Pb和Zn的含量均高于对照点且差异显著(P<0.05);4种重金属元素相比较,均以Zn含量最高,Cu含量次之,而Ni和Pb含量则较低;在不同器官中同一重金属元素的含量也有明显差异,其中,Cu、Ni和Zn含量均在腋芽中最高,Pb含量在2年生枝条中最高。4种重金属元素的累积量及其分布比例均在叶片中最高,在老树皮中次之,在1年生枝条、2年生枝条和腋芽中均较低;而4种重金属元素的污染指数及其分布比例则在老树皮中最高,在叶片中次之。研究结果显示：二球悬铃木各器官对空气中的重金属元素均有一定的吸滞能力,并且叶片和老树皮的吸滞能力明显优于其他器官。     

Evaluation of Atriplex Halimus,Medicago Lupulina and Portulaca Oleracea For Phytoremediation of Ni,Pb, and Zn

Suitable plant species are able to accumulate heavy metals and to produce biomass useful for non-food purposes. In this study, three endemic Mediterranean plant species, Atriplex halimus, Portulaca oleracea and Medicago lupulina were grown hydroponically to assess their potential use in phytoremediation and biomass production. The experiment was carried out in a growth chamber using half strength Hoagland's solutions separately spiked with 5 concentrations of Pb and Zn (5, 10, 25, 50, and 100 mg L^?1), and 3 concentrations of Ni (1, 2 and 5 mg L^?1). Shoot and root biomass were determined and analyzed for their metals contents. A. halimus and M. lupulina gave high shoot biomass with relatively low metal translocation to the above ground parts. Metals uptake was a function of both metals and plant species. It is worth noting that M. lupulina was the only tested plant able to grow in treatment Pb50 and to accumulate significant amount of metal in roots. Plant metal uptake efficiency ranked as follows: A. halimus > M. lupulina > P. oleracea . Due to its high biomass production and the relatively high roots metal contents, A. halimus and M. lupulina could be successfully used in phytoremediation, and in phytostabilization, in particular.     

Double complex salts of Pt and Pd ammines with Zn and Ni oxalates - promising precursors of nanosized alloys

Double complex salts [M(NH₃)₄][M′(Ox)₂(H₂O)₂] · 2H₂O (M = Pd, Pt, M′ = Ni, Zn) were synthesized by combination of solutions containing corresponding cations [M(NH₃)₄]²⁺ and anions [M′(Ox)₂(H₂O)₂]²⁻. The salts obtained were characterized by IR spectroscopy, thermal analysis, powder and single crystal X-ray diffraction. The prepared compounds are isostructural and crystallize in the orthorhombic crystal system (space group I222, Z = 2). Thermal decomposition of the salts in helium or hydrogen atmosphere at 200-400 °C results in formation of nano-sized bimetallic powders. Depending on the phase diagram of the respective bimetallic system and temperature conditions, they can be single phase or multiphase products. In particular, thermal decomposition of double complex salts [M(NH₃)₄][Zn(Ox)₂(H₂O)₂] · 2H₂O (M = Pd, Pt) results in formation of PdZn and PtZn intermetallic compounds, correspondingly. Decomposition of [Pd(NH₃)₄][Ni(Ox)₂(H₂O)₂] · 2H₂O affords a disordered solid solution Pd_0.5Ni_0.5. Disordered Pt_0.5Ni_0.5 was obtained from [Pt(NH₃)₄][Ni(Ox)₂(H₂O)₂] · 2H₂O in helium atmosphere, while in hydrogen atmosphere - a two-phase mixture of disordered Pt_0.5Ni_0.5 and ordered PtNi. In all cases crystallite sizes of bimetallic particles varied within 50-250 Å.     

Mononuclear Ni(II) and Zn(II) complexes of some potentially binucleating Schiff base ligands

Mononuclear Zn(II) and Ni(II) complexes have been prepared from two new Schiff base ligands in which two alternative co-ordination sites (N₂O₂ or O₂O₂) occur. The first ligands is the Schiff base derived from 1,2-diaminobenzene and 2-hydroxy-3-carboxyl-1-napthaldehyde (bopaH₄). The complexes of this ligand contain the metal ions in the N₂O₂ coordination site as a result of the steric requirements of the co-ordinated ligand. The second ligand series are derivatives of X-substituted 1,2-diaminobenzenes, 2-hydroxy-3-carboxy-1-naphthaldehyde and 2-hydroxy-5-methyl isophthaldehyde (X-bolaH₃). In this case Ni(II) occupies the N₂O₂ site in its complexes with the X-bolaH₃ ligands, whereas the Zn(II) complexes are co-ordinate through the O₂O₂ site since the steric restrictions are less severe.     

Study on synthesis, structure, and DNA-binding of Ni, Zn complexes with 2-phenylquinoline-4-carboylhydrazide

2-Phenylquinoline-4-carboylhydrazide (HL), and its novel nickel(II), zinc(II) complexes [M(HL)₂(L)]·2H₂O·NO₃ (M = Ni (1), M = Zn (2)), have been synthesized and characterized by elemental analysis, molar conductivity, and IR spectra. The crystal structure of [Ni(HL)₂(L)]·2H₂O·NO₃ obtained from ethanol solution was determined by X-ray diffraction analysis, crystallized in the rhombohedral system, space group , Z = 18, a = 31.913(3) Å, b = 31.913(3) Å, c = 27.709(2) Å, α = 90°, β = 90°, γ = 120°, R₁ = 0.0647. The interactions of the complexes and the ligand with calf thymus DNA had been investigated using UV-Vis spectra, fluorescent spectra, CD (circular dichroism) spectra, CV (cyclic voltammetry) and viscosity measurements. These compounds were tested against MFC (mouse forestomach carcinoma) cell lines. The complex 1 showed significant cytotoxic activity against MFC cell lines. The cleavage reaction on plasmid DNA has been monitored by agarose gel electrophoresis. Results suggest that the two complexes bound to DNA via a groove binding mode and the complexes can cleave pBR322 DNA.     

Thermodynamics of Ni2+, Cu2+, and Zn2+ binding to the urease metallochaperone UreE

The two Ni2+ ions in the urease active site are delivered by the metallochaperone UreE, whose metal binding properties are central to the assembly of this metallocenter. Isothermal titration calorimetry (ITC) has been used to quantify the stoichiometry, affinity, and thermodynamics of Ni2+, Cu2+, and Zn2+ binding to the well-studied C-terminal truncated H144*UreE from Klebsiella aerogenes, Ni2+ binding to the wild-type K. aerogenes UreE protein, and Ni2+ and Zn2+ binding to the wild-type UreE protein from Bacillus pasteurii. The stoichiometries and affinities obtained by ITC are in good agreement with previous equilibrium dialysis results, after differences in pH and buffer competition are considered, but the concentration of H144*UreE was found to have a significant effect on metal binding stoichiometry. While two metal ions bind to the H144*UreE dimer at concentrations <10 microM, three Ni2+ or Cu2+ ions bind to 25 microM dimeric protein with ITC data indicating sequential formation of Ni/Cu(H144*UreE)4 and then (Ni/Cu)2(H144*UreE)4, or Ni/Cu(H144*UreE)2, followed by the binding of four additional metal ions per tetramer, or two per dimer. The thermodynamics indicate that the latter two metal ions bind at sites corresponding to the two binding sites observed at lower protein concentrations. Ni2+ binding to UreE from K. aerogenes is an enthalpically favored process but an entropically driven process for the B. pasteurii protein, indicating chemically different Ni2+ coordination to the two proteins. A relatively small negative value of DeltaCp is associated with Ni2+ and Cu2+ binding to H144*UreE at low protein concentrations, consistent with binding to surface sites and small changes in the protein structure.     

Metal-regulated assemblies of Cu, Ni, and Zn complexes with isoquinoline-3-carboxylate displaying diverse supramolecular networks

Three distinct coordination complexes, viz. {[Cu(μ-L)₂] · (H₂O)₄}_n (1), [Ni(L)₂(CH₃OH)₂] (2), and [Zn(L)₂(H₂O)₂] · (H₂O)₂ (3), have been prepared by the reactions of metal nitrates with isoquinoline-3-carboxylic acid (HL). X-ray single-crystal diffraction suggests that 1 is a 1D chain coordination polymer in which the Cu^II ions are connected by carboxylates, whereas complexes 2 and 3 represent discrete mononuclear species. In all the cases, the coordination entities are further organized via hydrogen-bonding interactions to generate multifarious supramolecular networks. Remarkably, a well-resolved 1D water morphology is observed for the first time in the crystalline lattice of 1 along [1 0 0], which consists of edge-sharing tetrameric subunits and stabilized by the metal-organic host surroundings.     

El Niño mass coral mortality: a test of resource limitation in a coral reef damselfish population

Summary The mass mortality of reef corals in the eastern Pacific as a result of the 1982–1983 El Niño oceanographic anomaly permitted the first large scale test of resource limitation for a coral reef fish. Population densities of territorial herbivorous damselfish did not respond to the massive regional increase in space available for the cultivation of algal food following the El Niño event. The proportion of juveniles in the population was low and new recruits were uncommon, indicating that recruitment rates rather than resource supply probably control the abundance of this coral reef damselfish.     

Effects of pH on toxicity of As,Cr, Cu,Ni and Zn to Selenastrum capricornutum Printz

Acute toxicity tests were conducted to establish the response of Selenastrum capricornutum Printz to sublethal concentrations of As, Cr, Cu, Ni and Zn at a broad range of pH levels. Cultures were incubated for a period of seven days at pH 4 in standard algal assay media containing sublethal concentrations of metals. At this low pH, growth was depressed for all metals tested. The adjustment of pH to higher levels resulted in increased growth when cultures were treated with As, Cu, or Ni and incubated for an additional 7 days. Toxicity was least at the optimum pH range for growth of the alga.The observation that the toxicity of As, Cu, and Ni to S. capricornutum decreases markedly at pH values above 4.0 may be of ecological importance in the control of acid mine pollution. If a high percentage of algae show a similar response to decreasing toxicity with increasing pH, it clearly would be of value to adopt measures which control pH as well as the levels of metals present. It was suggested that algae with a broad pH growth range, such as S. capricornutum, could benefit from the addition of highly alkaline materials to waters where certain metals are present.