Spectral and thermodynamic properties of Ag(I), Au(III), Cd(II), Co(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(IV), and Zn(II) binding by methanobactin from Methylosinus trichosporium OB3b

Methanobactin (mb) is a novel chromopeptide that appears to function as the extracellular component of a copper acquisition system in methanotrophic bacteria. To examine this potential physiological role, and to distinguish it from iron binding siderophores, the spectral (UV–visible absorption, circular dichroism, fluorescence, and X-ray photoelectron) and thermodynamic properties of metal binding by mb were examined. In the absence of Cu(II) or Cu(I), mb will bind Ag(I), Au(III), Co(II), Cd(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(VI), or Zn(II), but not Ba(II), Ca(II), La(II), Mg(II), and Sr(II). The results suggest metals such as Ag(I), Au(III), Hg(II), Pb(II) and possibly U(VI) are bound by a mechanism similar to Cu, whereas the coordination of Co(II), Cd(II), Fe(III), Mn(II), Ni(II) and Zn(II) by mb differs from Cu(II). Consistent with its role as a copper-binding compound or chalkophore, the binding constants of all the metals examined were less than those observed with Cu(II) and copper displaced other metals except Ag(I) and Au(III) bound to mb. However, the binding of different metals by mb suggests that methanotrophic activity also may play a role in either the solubilization or immobilization of many metals in situ.     

Spectral and thermodynamic properties of Ag(I), Au(III), Cd(II), Co(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(IV), and Zn(II) binding by methanobactin from Methylosinus trichosporium OB3b

Methanobactin (mb) is a novel chromopeptide that appears to function as the extracellular component of a copper acquisition system in methanotrophic bacteria. To examine this potential physiological role, and to distinguish it from iron binding siderophores, the spectral (UV–visible absorption, circular dichroism, fluorescence, and X-ray photoelectron) and thermodynamic properties of metal binding by mb were examined. In the absence of Cu(II) or Cu(I), mb will bind Ag(I), Au(III), Co(II), Cd(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(VI), or Zn(II), but not Ba(II), Ca(II), La(II), Mg(II), and Sr(II). The results suggest metals such as Ag(I), Au(III), Hg(II), Pb(II) and possibly U(VI) are bound by a mechanism similar to Cu, whereas the coordination of Co(II), Cd(II), Fe(III), Mn(II), Ni(II) and Zn(II) by mb differs from Cu(II). Consistent with its role as a copper-binding compound or chalkophore, the binding constants of all the metals examined were less than those observed with Cu(II) and copper displaced other metals except Ag(I) and Au(III) bound to mb. However, the binding of different metals by mb suggests that methanotrophic activity also may play a role in either the solubilization or immobilization of many metals in situ.     

Controlling Factors and Pollution Assessment of Potentially Toxic Elements in Topsoils of the Issyk-Kul Lake Region,Central Asia

The Issyk-Kul Lake region is well known for its magnificent scenery and unique scientific significance. With multivariable statistical methods, the contents of several geochemical elements (Fe, Mn, V, Zn, Cr, Co, Ni, Cu, As, Mo, Cd, Sb, Tl, Pb, and Hg) and total organic matter of 61 topsoil samples were analyzed, and then, the results were used to assess the environmental factors controlling the concentrations of potentially toxic elements (PTE) in the region. The results showed that most of the elements including Fe, Mn, V, Cr, Co, Ni, Cu, As, and Sb reflected the natural state, but several PTE (Zn, Mo, Hg, Cd, Pb, and Tl) had been influenced by anthropogenic factors. Among these, Zn, Mo, Hg, and Cd were significantly correlated with the organic matter content, which suggests that agricultural soils will accumulate more PTE. From the calculations for the human risk assessment of anthropogenically derived PTE (Zn, Mo, Hg, Cd, Pb, and Tl), the risks for ingestion in this region were found to be higher than those for inhalation and dermal absorption; however, the results also suggested there are no non-carcinogenic risks for all anthropogenically influenced PTE in the current state.     

As(V) Reduction,As(III) Oxidation,and Cr(VI) Reduction by Multi-metal-resistant Bacillus subtilis,Bacillus safensis,and Bacillus cereus Species Isolated from Wastewater Treatment Plant

Industrial progress has resulted in threatening concentrations of toxic metals in various areas of the world. Bioremediation is an economical alternative to chemical methods. Bacteria resistant to As(III), As(V), Cr, Co, Cu, Cd, Hg, Ni, Pb, Se, and Zn were isolated from the wastewater treatment plant of Kasur, Pakistan. Highest resistance against all metals was exhibited by MX-1, MX-3, MX-4, and MX-5. The isolates possessed dual ability to oxidize as well as to reduce As. Highest As(V) reduction (454 µM) was exhibited by MX-1, while most As(III) oxidation was shown by MX-3 (170 µM). The isolates were also capable of reducing Cr(VI), and maximum Cr(VI) reduction (500 µM) was exhibited by MX-3. Transformation of DH5α with MX-1 plasmid showed that resistance genes for As(III), As(V), Cr, Cd, Se, Hg, and Ni were plasmid borne, while in case of MX-3, resistance genes for As(III), As(V), Co, Cu, Se, Pb, Zn, and Ni were present on plasmid. MX-1 and MX-3 were also positive for auxin production (37 and 32.96 µg ml^?1, respectively). MX-3 was also found to produce hydrogen cyanide (HCN) and solubilized phosphate. These isolates promoted plant (Vigna radiata) growth both in the presence and absence of the metals. MX-1, MX-3, and MX-5 were identified as Bacillus subtilis, Bacillus safensis, and Bacillus cereus through 16S rRNA gene sequencing, respectively. Such bacteria having multiple traits of resisting multiple metals, dual ability to oxidize/reduce As, and reduce Cr(VI) along with the ability to support plant growth are good tools for remediation of metal-contaminated sites and its cultivation.     

Heavy metals in water,sediments, fish and plants of river Hindon,U.P., India

We analysed the concentrations of Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn in the water, sediments, fish and plants of the River Hindon, U.P., India, at seven sampling stations, in the year 1982. Considerable variation in concentration between water, sediments, fish and plants were noted. The concentration in the water was in the order Fe > Zn > Cr > Mn > Cu > Pb > Ni > Co > Cd, in the sediments, Fe > Mn > Zn > Ni > Cr > - Co > Cu > Pb > Cd; in a fish (Heteropnuestes fossilis) Fe > Zn > Mn > Pb > Ni > Co > Cu > Cd > Cr, and in a plant (Eicchornia crassipes) Fe > Mn > Zn > Ni > Cu > Cr > Pb > Co > Cd.     

Reaction of some decomposer basidiomycetes to toxic elements

Høiland, K. 1995. Reaction of some decomposer basidiomycetes to toxic elements. -Nord. J. Bot. 15: 305–318. Copenhagen. ISSN 0107–055X.
Cultures of 15 decomposer basidiomycete samples were examined for resistance to Al. As, Be, Cd, Co, Cr, Cu, H, Hg₂(I), Hg(II), Ni, Pb, Sn, and Zn using a micro-well technique. Aluminium was found to be slightly toxic; Be, Zn, and As moderately toxic; Cr, Cu, Sn, Co, Hg(II), Ni, Hg₂(I), and Pb toxic: and Cd very toxic. Generally, the fungitoxicity rises with increasing electronegativity of the element, if we exclude As and Cd. According to the fungal reactions, the elements can be arranged into several groups with similar toxicity: The Cu-Hg₂(I)-Hg(II)-Ni group, the Al-Cr-H group, and the As-Pb-Zn group. Tin is related both to the first and the second group. Beryllium, Cd, and Co occupy more isolated positions. Resistance to Hg, Ni, and Cu generally increases with the ability of the fungus to produce phenoloxidases, especially the intracellular tyrosinase. One explanation may be that these fungi decompose the substances that actually bind Hg, Ni, and Cu and hence protect them from the toxic action. Resistance to A1 and H (expressed as pH) may be higher in fungi from poor soils. The physiological effect of soluble A1 on fungi seems to depend more on its ability to release H₃O+ in the medium than on the toxic action of the metal itself. On the other hand, resistance to Cd is possibly higher in fungi from rich soils, probably because toxicity of Cd usually increase with pH.     

浙江油茶产地土壤和果实金属元素含量特征

为探讨油茶(Camellia oleifera)产地土壤和油茶果实中金属元素分布和富集特征,在油茶果实成熟期,对浙江5个油茶产地土壤及油茶果实中金属元素进行污染分析和富集能力评价。结果表明,浙江油茶产地土壤中Pb、Cr、Cd、As、Hg、Ni、Cu和Zn含量低于农用地土壤污染风险筛选值,综合污染等级为安全。个别产区常山县土壤中As、Ni、Cu和江山县土壤中Pb、Cr、Fe含量显著高于其他产地;常山和建德土壤中Cd单因子污染指数分别为0.93和0.81,处于污染警戒线。Cr、Ni、Cu、Zn主要分布在油茶籽中,Hg主要分布在壳中,Pb、Cd、As、Fe和Mn主要分布在青皮中。油茶籽中Cu、Fe、Mn的富集系数大于0.4,吸收能力强,Ni、Zn的富集系数小于0.4,具有一定吸收能力,Pb、Cr、Cd、As和Hg的富集系数小于0.1,吸收能力低;壳中Cu、Mn的富集系数大于0.4,吸收能力强,Fe的富集系数小于0.4,具有一定吸收能力,Pb、Cr、Cd、As、Hg、Ni、Zn的富集系数小于0.1,吸收能力低;青皮中Cu、Fe、Mn的富集系数大于0.4,吸收能力强,Pb、Cr、Cd、As、Hg、Ni、Zn的富集系数小于0.1,吸收能力低。浙江油茶主产区土壤质量安全,适合油茶种植。油茶果实对Cu、Fe、Mn有一定富集能力,对Pb、Cr、Cd、As和Hg无富集能力。     

Assessment of water quality and health risks for toxic trace elements in urban Phewa and remote Gosainkunda lakes,Nepal

The concentration of 13 metals (Al, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Cd, Pb, and Hg) and their associated health risk assessment was performed for two Himalayan lakes, urban Phewa and remote Gosainkunda, from Nepal. Water Quality Index (WQI), Metal Index (MI), Hazard Quotient (HQ), Hazard Index, and Cancer Risk were calculated in order to evaluate the water quality of these lakes. Correlation analysis revealed that Mn and Fe were derived from natural geological weathering processes and Pb, V, Cr, Co, Ni, Cu, Zn, and Cd might have originated from anthropogenic sources. The results revealed that WQI of the remote lake fell into excellent water quality and urban lake fell into poor water quality, which is also supported by the MI calculation. Moreover, the HQ of Mn in urban lake showed values greater than unity suggesting its health risk to the local inhabitants. The cancer index values indicated “high” risk due to Cr, whereas Cd possesses “very low” cancer risk on local population residing nearby areas. This study provides the useful database and suggests for the regular assessment and policy formulation for safeguarding the natural water bodies in the region.     

Metals in some dominant vascular plants, mosses, lichens, algae, and the biological soil crust in various types of terrestrial tundra, SW Spitsbergen, Norway

Arctic environments are commonly considered to be relatively pristine because of minimal local human activity. However, these areas receive air pollution from lower latitude regions. Our goal was to determine concentrations of metals (Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, and Zn) in dominant species of vascular plants, mosses, lichens, algae, and in the biological soil crust (BSC), and topsoil (0–3 cm) from various types of tundra in the southwestern part of Spitsbergen, Norway. Results indicate that mosses are more efficient bioaccumulators of Cd, Co, Cr, Cu, Fe, Mn, and Zn than lichens. The highest levels of Co, Cr, Cu, Fe, Hg, Mn, Ni, and Pb were found in the BSC, and the moss species Racomitrium lanuginosum, Sanionia uncinata, and Straminergon stramineum from the polygonal tundra, initial cyanobacteria-moss wet tundra, snow bed cyanobacteria-moss tundra, and flow water moss tundra alimented by melting ice or snow. The observed higher concentrations of Cu and lower concentrations of Hg in mosses, lichens, and vascular plants compared with values observed 20 years earlier were apparently associated with changes in the atmospheric deposition of contaminants over Spitsbergen due to changes in the long-distance transport of anthropogenic emissions from industrialized areas. Prasiola crispa and Salix polaris may be useful bioindicators of Cd and Zn, and the BSC, R. lanuginosum, S. uncinata, and S. stramineum as bioindicators of Co, Cr, Cu, Fe, Hg, Mn, Ni, and Pb. These results may be extrapolated across other areas of Spitsbergen with similar climates.     

Comparative Evaluation of Trace Metal Distribution and Correlation in Human Malignant and Benign Breast Tissues

Selected trace metals were analyzed in human malignant and nonmalignant (benign) breast tissue samples by the flame atomic absorption spectrophotometric method. In malignant tissues, dominant mean concentrations were revealed by Na, K, Ca, Mg, Fe, Zn, and Al at 927, 552, 231, 61.7, 36.5, 18.3, and 8.94 microg/g, respectively, while the mean metal levels in benign tissues were 903, 435, 183, 63.3, 24.7, 14.5, and 10.1 microg/g, respectively. Average concentrations of Cd, Co, Cr, Cu, Fe, Mn, K, Ca, and Zn were noted to be significantly higher in the malignant tissues compared with the benign tissues. Significantly strong correlations (r > 0.50) in malignant tissues were observed between Mn and Co, Mn and Cd, Cd and Cr, Fe and Mn, Cd and Co, Fe and Co, Mg and Pb, Cd and Fe, Mg and Ni, Pb and Ni, Ni and Sr, and Fe and Pb, whereas, Cd and Co, Cd and Mn, Co and Mg, Co and Mn, Cu and Mn, Co and Ni, Mg and Ni, Cd and Cu, Cd and Ni, Ca and Mg, Mn and Pb, Cu and Ni, Fe and Ni, Cd and Mg, Co and Cu, Cr and Na, and Cd and Cr revealed strong and significant relationships in benign tissues at p < 0.001. Principal component analysis of the metals data yielded six principal components for malignant tissues and five principal components for benign tissues, with considerably different loadings, duly supported by cluster analysis. The study revealed a considerably different pattern of distribution and mutual correlations of trace metals in the breast tissues of benign and cancerous patients.     

The copper-enzyme dopamine beta-monooxygenase: studies on the ability of several metals to inhibit the enzyme activity and to replace the copper

The ability of several metals to inhibit dopamine beta-monooxygenase was measured and compared with their ability to compete with the binding of 64Cu to the water-soluble form of the bovine adrenal enzyme at pH 6.0. In the presence of an optimal concentration of copper (0.5 microM in the present assay system), an inhibition was observed upon addition of Hg(II), Zn(II), or Ni(II). Only a small fraction of the inhibition with these metals may be due to uncoupling of electron transport from hydroxylation. Preincubation of these metals with the Cu-depleted apoenzyme before addition of copper, revealed a stronger inhibition than if copper was added before the other metals. Hg(II), Zn(II), and Ni(II) also compete with the binding of 64Cu(II) to the protein. Hg(II) was the most effective and Ni(II) the least effective of these metals, both with respect to inhibition of the enzyme activity and to prevent the binding of 64Cu(II). Competition experiments on the binding of Zn(II) and 64Cu in the presence and absence of ascorbate, indicated i) a similar affinity of Cu(I) and Cu(II) to the native enzyme, and ii) a more rapid binding of Cu(I) than Cu(II) to the Cu-depleted and Zn-containing enzyme. Al(III), Fe(II), Mg(II), Mn(II), Co(II), Cd(II), and Pb(II) neither inhibited the enzyme activity nor competed with the binding of 64Cu(II) to the protein (Fe(II) was not tested for binding). Of those metals cited above only Cu(II)/Cu(I) was able to reactivate the apoenzyme.     

Studies on the Characteristic of Element Contents in the Dominant Plant Species of the Three gorges Region in China

The characteristics of the contents of 20 elements (Al, Fe, Mn, Ca, Mg, K, S, Si, P, Cd, Cu, Zn, Ti, Ni, Sr, Mo, Na, B, Cr, V) in 16 plant species collected from the Three Gorges Region in China were investigated. The average contents of Ca, K and Mg were higher than 1 000 μg·g-1, that of Al, P, Si, Fe, S and Mn ranged between 100—1 000 μg·g-1 and Ti, Cu, Ni, Cr, Mo, Cd and V were less than 10 μg·g- 1. The level of Na content was less than that of the reported. The main character of the element contents was of the Ca> K type. The contents of P, S, Ca and K in different plant samples showed a normal distribution pattern, while Al and Mn showed a elements lognormal distribution pattern. Plant species differed greatly in the element contents. On analyzing the coefficient of variation (C. V., % ), Al, Mn, Mg, Ni, Sr and Fe had higher C.V., while the C.V. of K, S, P, Cr, Cd and Cu was less than 60%, and Cu had the lowest C.V. The correlations between Al and Fe, Al and Ti, Al and Cr, A1 and V, Cd and Sr, Cd and Mo, Fe and V, Zn and Cr, Ni and Sr, Mg and Ni, Mo and Sr, Ca and Sr, Cr and Mo, Na and Mg, Na and P, P and S were statistically significant in different plant species. The classification of the 16 plant species and 20 dements by two-way indicator species analysis (TWINSPAN) method may suggest the difference in dement contents of the different plant species.     

Study of the mutagenicity of metal derivatives with Salmonella typhimurium TA102

The mutagenic potential of 16 metal derivatives was studied with a new mutant of Salmonella typhimurium, the strain TA102 (Levin et al., 1983). Some of these compounds are known as carcinogens (As, Cr VI, Cd, Ni) or suspected carcinogens in man (Pb, Hg), others are known as non-carcinogens (Cr III, Al, Cu, Mn, Fe). Among these 16 derivatives, only the two Cr(VI) compounds are strong mutagens (K2Cr2O7 or K2CrO4).     

Applicability of Heavy-Metal Phytoextraction in United Arab Emirates: An Investigation of Candidate Species

Phytoremediation of contaminated calcareous desert land in the United Arab Emirates has been investigated. Soils from 12 northern UAE sites, suspected of metal contamination, were acid-extracted and analyzed by ICP-OES for Co, Cr, Cu, Fe, Mn, Ni, Pb, and Zn. Twenty-two plants naturally growing at contaminated sites were sampled and analyzed for their uptake of Co, Cr, Cu, Mn, Ni, Pb, and Zn and eight commercially available plants, grown under controlled conditions, were also studied for their phytoextraction capabilities. The concentration of available Cr was found to be 1300 ± 150 mg/kg in the soil of the Ajman Industrial Zone and 80 ± 10 mg/kg of Pb was found at Bithna. Among the plants investigated, Portulaca oleracea and Iresine herbstii showed potential for Cr(VI) and Pb(II) accumulation, respectively, with bioconcentration factors (BCF) greater than unity. Atriplex halimus accumulated Co(II), Cr(III), and Cu(II) each with a BCF > 1.     

Adsorption of heavy metal ions from aqueous solutions by activated carbon prepared from apricot stone

Apricot stones were carbonised and activated after treatment with sulphuric acid (1:1) at 200 degrees C for 24 h. The ability of the activated carbon to remove Ni(II), Co(II), Cd(II), Cu(II), Pb(II), Cr(III) and Cr(VI) ions from aqueous solutions by adsorption was investigated. Batch adsorption experiments were conducted to observe the effect of pH (1-6) on the activated carbon. The adsorptions of these metals were found to be dependent on solution pH. Highest adsorption occurred at 1-2 for Cr(VI) and 3-6 for the rest of the metal ions, respectively. Adsorption capacities for the metal ions were obtained in the descending order of Cr(VI) > Cd(II) > Co(II) > Cr(III) > Ni(II) > Cu(II) > Pb(II) for the activated carbon prepared from apricot stone (ASAC).     

Microbial reduction of metals and radionuclides

The microbial reduction of metals has attracted recent interest as these transformations can play crucial roles in the cycling of both inorganic and organic species in a range of environments and, if harnessed, may offer the basis for a wide range of innovative biotechnological processes. Under certain conditions, however, microbial metal reduction can also mobilise toxic metals with potentially calamitous effects on human health. This review focuses on recent research on the reduction of a wide range of metals including Fe(III), Mn(IV) and other more toxic metals such as Cr(VI), Hg(II), Co(III), Pd(II), Au(III), Ag(I), Mo(VI) and V(V). The reduction of metalloids including As(V) and Se(VI) and radionuclides including U(VI), Np(V) and Tc(VII) is also reviewed. Rapid advances over the last decade have resulted in a detailed understanding of some of these transformations at a molecular level. Where known, the mechanisms of metal reduction are discussed, alongside the environmental impact of such transformations and possible biotechnological applications that could utilise these activities.     

Pollution Assessment and Potential Sources of Heavy Metals in Agricultural Soils around Four Pb/Zn Mines of Shaoguan City,China

A total of 455 agricultural soil samples from four nonferrous mines/smelting sites in Shaoguan City, China, were investigated for concentrations of 10 heavy metals (As, Cd, Co, Cr, Cu, Hg, Mn, Ni, Pb, and Zn). The mean concentrations of the metals were 72.4, 5.16, 13.3, 54.8, 84.5, 1.52, 425, 28.2, 529, and 722 mg kg^?1, respectively. The values for As, Cd, Hg, Pb, and Zn were more than 8 and 1.5 times higher than their background values in this region and the limit values of Grade II soil quality standard in China, respectively. Estimated ecological risks based on contamination factors and potential ecological risk factors were also high or very high for As, Cd, Hg, and Pb. Multivariate analysis (Pearson's correlation analysis, hierarchical cluster analysis, and principal component analysis) strongly implied three distinct groups; i.e., As/Cu/Hg/Zn, Co/Cr/Mn/Ni, and Cd/Pb. Local anomalies for As, Cu, Hg, and Zn by a probably anthropogenic source (identified as mining activity), Co, Cr, Mn, and Ni by natural contribution, and a mixed source for Cd and Pb, were identified. This is one of the few studies with a focus on potential sources of heavy metals in agricultural topsoil around mining/smelting sites, providing evidence for establishing priorities in the reduction of ecological risks posed by heavy metals in Southern China and elsewhere.     

奉节脐橙不同器官元素含量分布特征

对奉节脐橙果、叶、干、根中的必需大量元素 (N、K、Ca、Mg、P、S)、微量元素 (Fe、Mn、Cu、Zn、B、Mo)、有益元素 (Si、Co、F、Se、Ni、Sr)、有毒有害元素 (Hg、As、Cr、Cd、Pb、Sb、Bi)的分布特征进行分析 ,结果表明 :果、叶、干、根对各元素的吸收与富集特征具有明显的规律性 ,如叶、干、根中大量元素含量次序均为 Ca>N>K>Mg,叶、干、根中微量元素含量均有 Fe>Mn>Zn>Cu>Mo的规律 ,根、干、叶中有益微量元素含量次序均为 Si>Sr>F>Ni>Co>Se,叶、干、根中有毒有害元素含量次序均有 Pb>As>Sb >Hg的规律 ;在脐橙各器官中 ,叶是大量元素与有毒有害元素最富集的器官 ,根则是有益元素最富集的器官 ,有毒有害元素的 Cr、微量元素的 Mn、Fe、Mo也以根最为富集 ,干则是上述元素最不富集的器官 ,所有元素中 ,仅 Zn在干中最富集 ;大量元素 (除 N外 )、微量元素、有益元素在脐橙各器官的分配含量与地壳土壤背景值的分异含量趋势基本一致 ,土壤背景是这三类元素的主要控制因素。但有毒有害元素的分配形式则明显受人类活动的影响     

Synthesis, spectroscopic, and antitumor activity of metal chelates of S-methyl-N-(l-isoquinolyl)-methylendithiocarbazate

Complexes of Mn(III), Fe(III), Fe(II), Co(III), Ni(II), Cu(II), Zn(II), and Pt(II) with S-methyl-N-(l-isoquinolyl) methylendithiocarbazate (N-N-SH) were isolated and characterized by elemental analysis, conductance measurement, magnetic susceptibilities, and spectroscopic studies. On the basis of these studies, a highly distorted, high-spin, chloro-bridged, polymeric octahedral structure for [Mn(N-N-S)Cl2]; a distorted, low-spin, monomeric octahedral structure for [Fe(N-N-S)2]; a distorted, high-spin, octahedral structure for [Ni(N-N-S)2]; and a square-planar structure for [M(N-N-S)X] (M = Ni, Cu, Pt or Zn and X = Cl- or -OAc) are suggested. With Fe(III), the complex [Fe(N-N-S)2][FeCl4] was isolated while the Co(II) was oxidized to yield the Co(III) ion as [Co(N-N-S)2]2[CoCl4]. All these complexes were screened for their antitumor activity against P 388 lymphocytic leukemia test system in mice. Except for Mn(III), Fe(III), and Co(III) complexes, all were found to possess significant activity; the Cu(II) and Zn(II) complexes showed a T/C% value of 160 and 195, respectively, at their optimum dosages.     

Minor and trace elements in human milk from Guatemala,Hungary, Nigeria,Philippines, Sweden,and Zaire

Concentrations of As, Ca, Cd, Cl, Co, Cr, Cu, F, Fe, Hg, I, K, Mg, Mn, Mo, Na, Ni, P, Pb, Sb, Se, Sn, V, and Zn were determined in human whole milk samples from Guatemala, Hungary, Nigeria, Philippines, Sweden, and Zaire; in most of these countries, three groups of subjects representing different socioeconomic conditions were studied. Analytical quality control was a primary consideration throughout. The analytical techniques used were atomic absorption spectrophotometry, atomic emission spectrometry with an inductively coupled plasma, colorimetry, electrochemistry, using an ion-selective electrode and neutron activation analysis. The differences between median concentrations of Ca, Cl, Mg, K, Na, and P (minor elements) were lower than 20% among the six countries. Among trace elements, concentrations observed in Filipino milk for As, Cd, Co, Cr, Cu, F, Fe, Mn, Mo, Ni, Pb, Sb, Se, and V were higher than for milk samples from other countries. The remaining five countries showed a mixed picture of high and low values. In the case of at least some elements, such as, F, I, Hg, Mn, Pb, and Se, the environment appears to play a major role in determining their concentrations in human milk. The nutritional status of the mother, as reflected by her socioeconomic status, does not appear to influence significantly the breast milk concentrations of minor and trace elements. Significant differences exist between the actual daily intakes observed in this study and current dietary recommendations made by, for example, WHO and the US National Academy of Sciences. These differences are particularly large (an order of magnitude or more!) for Cr, F, Fe, Mn, and Mo; for other elements, such as, Ca, Cu, Mg, P, and Zn, they amount to at least a factor 2. In the opinion of the present authors, these findings point to the need for a possible reassessment of the dietary requirements of young infants with respect to minor and trace elements, particularly for the elements Ca, Cr, Cu, F, Fe, Mg, Mn, Mo, P, and Zn.