Accumulation and detoxification of cadmium in <Emphasis Type="Italic">Brassica pekinensis</Emphasis> and <Emphasis Type="Italic">B. chinensis</Emphasis>

The effect of excessive Cd on the growth and metal uptake by leafy vegetables Brassica chinensis L. (cv. Wuyueman) and Brassica pekinensis (Lour.) Rupr. (cv. Qingyan 87-114) were studied in hydroponic solution culture. The Cd concentration higher than 10 μM significantly decreased the root elongation and leaf chlorophyll contents of both plant species. The shoots of B. pekinensis had significantly higher concentrations of total and water-soluble Cd than B. chinensis. The roots of both species accumulated more Cd than the shoots in all the Cd treatments. Most of the Cd in the roots was found in the cell walls. The shoot/root ratio of Cd concentrations in B. pekinensis was always greater than that in B. chinensis. But, the concentration and proportion of Cd in the cell walls in B. chinensis were higher than that in B. pekinensis. Cadmium treatments also increased the concentrations of total non-protein thiols (NPT) in the shoots of the both species. A significant correlation was found between the concentrations of soluble Cd and NPT in plant shoots.     

高浓度镉、锌及其复合作用对烟草抗氧化系统的影响

采用水培方法,研究高浓度镉(0.1 mmol·L^-1 Cd²⁺)、锌(0.15 mmol·L^-1 Zn²⁺)及其复合作用(0.1 mmol·L^-1 Cd²⁺+0.15 mmol·L^-1Zn²⁺)对烟草种子的萌发率、幼苗叶片活性氧(ROS)水平、抗氧化物浓度、抗氧化酶活性及膜脂过氧化程度的影响.结果表明: 单因子条件下,与对照相比,高浓度镉、锌处理烟草种子萌发率降低;叶片超氧自由基(O₂^-· )产生速率与过氧化氢(H₂O₂)含量升高;过氧化氢酶(CAT)、抗坏血酸过氧化物酶(APX)、脱氢抗化血酸还原酶(DHAR)、单脱氢抗坏血酸还原酶(MDAR)和谷胱甘肽还原酶(GR)活性升高;谷胱甘肽(GSH)含量及其与氧化型谷胱甘肽比值(GSH/GSSG)下降;丙二醛(MDA)含量升高.与镉、锌单因子处理相比,镉、锌复合处理的烟草种子萌发率显著升高;O₂^-· 产生速率、H₂O₂和MDA含量降低;CAT、APX、MDAR活性在处理末期升高.镉、锌胁迫对烟草可造成生理水平上的损伤,且毒性效应随着处理时间的延长而增强.镉、锌复合作用可缓解镉、锌单因子胁迫对烟草幼苗的毒害.     

Subcellular Distribution of Cadmium and Nickel in Chronically Exposed Wild Fish: Inferences Regarding Metal Detoxification Strategies and Implications for Setting Water Quality Guidelines for Dissolved Metals

The objective of this study was to investigate metal detoxification in chronically exposed juvenile yellow perch (YP: Perca flavescens) and to field test the commonly assumed threshold toxicity model. Fish were collected from lakes located along a cadmium (Cd) and nickel (Ni) concentration gradient. Ambient dissolved metal concentrations were measured to evaluate exposure and total hepatic metal concentrations were determined as a measure of metal bioaccumulation. Hepatic metal partitioning among potentially metal-sensitive fractions (heat-denatured proteins, organelles) and detoxified metal fractions (metallothionein) was determined after differential centrifugation of YP liver homogenates. Major proportions of hepatic Cd were found in the heat-stable cytosolic peptides and proteins fraction (HSP; including metallothioneins), whereas Ni was mainly found in the potentially metal-sensitive heat-denaturable proteins fraction (HDP). For these chronically exposed fish there was no threshold exposure concentration below which binding of Cd or Ni to the heat-denaturable protein fraction or the organelle fraction did not occur. Metal detoxification was clearly incomplete and P. flavescens was subject to some metal-related stress, as evidenced notably by endocrine perturbations. Similar subcellular partitioning results were obtained when juvenile yellow perch were transferred from a reference lake to a Cd-contaminated lake and Cd accumulation was followed over time; there was no accumulation threshold below which Cd binding to the putative metal-sensitive fractions (HDP and organelles) did not occur. The presence of Cd and Ni in these fractions, even for low exposure concentrations and low hepatic accumulation, contradicts the threshold toxicity model that underpins metal toxicology theory and that is implicitly used in setting water quality guidelines for metals. Chronically exposed YP appear to have settled for a tradeoff between the cost of turning on their detoxification apparatus at full capacity, to completely suppress metal binding to metal-sensitive sites, and the alternative cost of allowing some binding of inappropriate metals to metal-sensitive sites.     

Pot experiment to study the uptake of Cd and Pb by three Indian mustards (Brassica juncea) grown in artificially contaminated soils

Most of the metals-contaminated and fallow lands in Taiwan are a result of irrigation with illegal effluent of factories. Phytoextraction methods can be applied to reach the target of fallow-lands reuse and earn more incomes for farmers. In many studies, Indian mustards (Brassica juncea) were planted in the metal-contaminated soils to study their suitability in phytoextraction. However, the total removal of metals by plants was quite different between accessions. In this pot study, three accessions of B. juncea (cv. 182921, cv. 211000, and cv. 426308) were planted in artificially Cd- or Pb-contaminated soils to investigate the differences between them. EDTA was applied to study its effect in increasing the bioavailability of Cd and Pb and their uptake by these Indian mustards. Experimental result showed that three accessions of Indian mustard can accumulate a high concentration of Cd and Pb when growing in the artificially Cd- and Pb-contaminated soils. Their shoot Cd or Pb concentrations were significantly enhanced, resulting from the application of EDTA. Among the three accessions, B. juncea cv. 211000 accumulated the highest concentrations of Cd and Pb in their shoots compared with B. juncea cv. 182921 and cv. 426308, but its total removal was the lowest due to its lower biomass.     

小麦幼苗生长及其抗氧化酶活性对模拟酸雨与金属离子复合胁迫的响应

通过水培试验,研究了模拟酸雨(pH 3.5)与Al(3、30 mg/L)、Pb(25、250 mg/L)、Cd(0.11、mg/L)单独或复合胁迫对小麦幼苗生长及抗氧化酶活性的影响。结果表明,模拟酸雨与Al、Pb、Cd单独或复合处理12 d后,小麦幼苗根长降低54.01%~94.81%,苗高降低18.88%~77.95%,单粒萌根数降低21.87%~80.37%,其生长发育受到显著抑制,抑制效应随处理浓度增大和作用时间延长而增强,且复合处理组抑制效应更强;幼苗根部超氧化物歧化酶(SOD)活性在模拟酸雨与单一金属离子处理下显著升高,而在3种金属离子复合处理下显著降低,但酸性条件下无论金属离子单独及复合处理后,过氧化物酶(POD)活性均显著升高,过氧化氢酶(CAT)活性均明显下降。研究发现,酸性条件下3种金属离子对植物细胞均产生氧化胁迫作用,且它们复合胁迫的毒性效应大于其单独胁迫。     

Preparation and characterization of two novel three-dimensional supramolecular networks with blue photoluminescence

Two novel photoluminescent coordination polymers of formula [Cd(atpt)(H₂O)₂] · 2H₂O (1) and [Zn(atpt)(H₂O)₂] (2) (H₂atpt = 2-aminoterephthalic acid), in which the amino group of the atpt ligand coordinates to the metal(II) ions for the first time, have been synthesized through the self-assemblies of H₂atpt and N-containing ligands [nicotiamide for 1 and imidazole for 2, respectively] with the metal(II) ions in the presence of NaOH. These complexes were characterized by FT-IR spectroscopy, thermogravimetric analysis (TG), elemental analysis and X-ray analysis. X-ray crystallographic studies of the complexes reveal that complex 1 is a double stranded one-dimensional chain, which further assembles into a three-dimensional supramolecular network via the interchain π-π stacking interaction and strong hydrogen bonds, while complex 2 exhibits a two-dimensional porous architecture. The extensively strong hydrogen bonds in complex 2 lead to the formation of three-dimensional supramolecular framework. Photoluminescence properties of the compounds 1 and 2 have been examined in solid state at room temperature. These compounds have been found to exhibit blue photoluminescence and may be good candidates for photoactive materials.     

重金属镉（Cd）和增强UV—B辐射复合对大豆生长和生理代谢的影响

研究了大豆的生长、生物量、抗氧化酶活性和吲哚乙酸（IAA）氧化酶活性在Cd^2 、UV－B辐射和二者复合胁迫（Cd UV-B)下的变化。结果表明,Cd^2 和UV－B辐射都抑制大豆生长,并显著抑制根的伸长,二者复合后加强了对根伸长的抑制。UV－B辐射显著增强了POD、SOD活性,Cd^2 对POD活性影响不明显,但却拮抗UV－B对POD活性的诱导,SOD活性在各种胁迫下显著增强。虽然Cd%2 对叶片类黄酮含量影响不明显,但对UV－B诱导的类黄酮合成有一定影响。IAA氧化酶活性在复合作用下下降,可能是复合胁迫影响大豆生长的重要因素之一。     

The synthesis, crystal and molecular structures of two saccharinate-metal complexes with dipyridylamine (dipyr) as a co-ligand

The complexes [Cd(dipyr)₂(sac)(H₂O)] sac·H₂O 1 and [Hg(dipyr)(sac)₂] 2, where dipyr = dipyridylamine and sac = saccharinate, have been synthesised, and fully characterised by single-crystal X-ray diffraction at 120 K. The geometry around Cd in 1 is approximately octahedral, with the metal coordinated by two bidentate dipyr ligands, one N-bonded sac and one H₂O molecule; the second sac forms the counter-ion, and there is also a water of crystallisation. An extensive H-bonded network is formed. In the anhydrous Hg complex 2, the metal has approximately tetrahedral geometry, with coordination from a bidentate dipyr ligand and two N-bonded sac groups. H-bonding interactions are again extensive, even without the presence of H₂O molecules in the structure, leading to chains along the a-axis.     

Coordination compounds of Cd(II) with several bidentate-NN′ and tridentate-NN′N nitrogen donor ligands. Cd NMR studies of monomeric compounds containing nitrogen donor atoms

Reaction of CdCl₂ with N-alkylaminopyrazole ligands 1-[(2-ethylamino)ethyl]-3,5-dimethylpyrazole (deae), 1-[(2-(tert-butylamino)ethyl)]-3,5-dimethylpyrazole (deat), bis-[(3,5-dimethylpyrazolyl)methyl]ethylamine (bdmae), and bis-[(3,5-dimethylpyrazolyl)ethyl]ethylamine (ddae) in absolute ethanol yields [CdCl₂(NN′)] (NN′ = deae (1), deat (2)), [CdCl₂(bdmae)] (3), and [CdCl(ddae)]₂[CdCl₄] (4). The Cd(II) complexes have been characterised by elemental analyses, conductivity measurements, IR, ¹H, ¹³C{¹H} and ¹¹³Cd NMR spectroscopies, and X-ray diffraction methods. ¹H and ¹¹³Cd NMR experiments at variable temperature for 3 and 4 show that dynamic processes are taking place in solution. We report the measurements of ¹¹³Cd NMR chemical shift data for complexes 1-4 in solution. X-ray crystal structures for complexes 2 and 3 have been determined. The Cd(II) is coordinated to the deat ligand, in 2, by one nitrogen atom of the pyrazolyl group and one nitrogen atom of the amine. It finishes a tetrahedral geometry with two chlorine atoms. The bdmae ligand is linked to Cd(II), in 3, by two nitrogens atoms of the pyrazolyl groups and one amine nitrogen, along with two chlorine atoms, in a distorted trigonal bipyramidal geometry.     

Cd-Cu复合胁迫对黄菖蒲叶片及根系中Cd和Cu的积累及其迁移率的影响

采用水培法研究了Cd-Cu复合胁迫(5 mg·L-1Cd-10 mg·L-1Cu;5 mg-L-1Cd-20 mg·L-1Cu;25 mg·L-1 Cd-10 mg·L-1Cu;25 mg·L-1Cd-20 mg·L-1Cu)条件下黄菖蒲(Iris pseudacorus L.)叶片和根系对Cd和Cu的积累作用及黄菖蒲体内Cd和Cu迁移率的变化规律.结果表明,在50 d的胁迫期内,黄菖蒲叶片和根系中的Cd和Cu含量分别随培养液中Cd和Cu浓度的提高而增加,并随胁迫处理时间的延长基本呈增加的趋势,在胁迫末期明显提高.在不同浓度Cd-Cu复合胁迫条件下,黄菖蒲根系中的Cd和Cu积累量明显高于叶片.在Cd浓度不变的条件下,黄菖蒲叶片和根系中的Cd含量随培养液中Cu浓度的提高而增加;在Cu浓度不变的条件下,黄菖蒲叶片中Cu含量随培养液中Cd浓度的提高而降低.在不同胁迫时间,黄菖蒲植株对Cd的迁移率不同,但培养液中Cd的浓度较高,黄菖蒲植株对Cd的迁移率也较高;黄菖蒲植株对Cu的迁移率随胁迫时间的延长基本上呈上升趋势.研究结果显示,在Cd-Cu复合胁迫条件下,Cu对黄菖蒲体内Cd的吸收具有一定的协同吸收作用,而Cd对Cu的吸收则有一定的拈抗作用.