Study on increase in toxicity of Schiff bases on microorganism on chelation with metal

New heterochelates of the type [M(L)(SB)(H₂O)] (where M?=?Mn(II), Co(II), Ni(II), Cu(II), Zn(II), and Cd(II), KHL?=?potassium salt of salicylideneglycine and SB?=?thiophene- O -carboxaldeneaniline) have been synthesized. The heterochelates have been characterized on the basis of elemental analyses, electronic spectra, and magnetic measurement analyses. The structural and geometrical conformation has been discussed on the basis of IR spectral data. A thermal study of the complexes has been carried out to ascertain their thermal stability. Magnetic susceptibility measurements and electronic spectral data suggest a six-coordinated octahedral structure for these complexes. The increase in toxicity of the investigated heterochelate metal compounds was tested against three gram-negative bacteria, S. typhi, E. coli, and Serratia marcescens by the disc diffusion method. It is observed that the heterochelates show higher toxicity when compared to the Schiff bases, metal salts, and control (DMSO) due to chelation. The toxicity is also compared to the standard drug tetracycline.     

Synthesis,structural elucidation,electro-chemical behaviour and fungitoxic activity of transition metal(II) mixed-ligand complexes with some Schiff bases

The Schiff bases, potassium salt of salicylidene-β-alanine [KHL], bis(benzylidene)ethylenediamine [SB¹] and thiophene-o-carboxaldene-p-toluidine [SB²], and mixed-ligand complexes with Mn(II), Co(II), Ni(II), Cu(II), Zn(II), and Cd(II) have been prepared. They were characterized by elemental analyses, magnetic susceptibility measurements, thermogravimetric analyses (t.g.a.), infrared spectra and electronic spectra. The mixed-ligand complexes were found to have the general composition [M(L)(SB)(H₂O)]. All the mixed-ligand complexes were found to have six-coordinated octahedral geometry. The fungitoxic activity of the ligands, metal salts, control (DMSO), bavistin, emcarb, and mixed-ligand complexes were screened against Aspergillus niger, Fusarium oxysporum and Aspergillus flavus. All the mixed-ligand complexes show higher fungitoxic activity as compared to the Schiff bases, metal nitrate and control (dimethyl sulphoxide, DMSO), and moderate fungitoxic activity as compared to the fungicides (bavistin and emcarb).     

Spectroscopic studies and biological evaluation of some transition metal complexes of a novel Schiff base ligands derived from 5-arylazo-salicyladehyde and o-amino phenol

Synthesis and characterization of Cu(II), Ni(II), and Zn(II) Schiff bases complexes resulted from the condensation of salicylaldehyde derivatives with o-amino phenol were discussed using elemental analysis (carbon, hydrogen, and nitrogen), molar conductance, magnetic measurements, mass spectra, and electronic spectra. The essential bands of infrared, ¹HNMR, and UV-Vis spectra as well as thermogravimetric analysis corresponding to the active groups within the three ligands and their complexes were interpreted. The dehydration and decomposition processes of the [Cu(H₂L₁)(H₂O)](OAc)₂, [Ni(H₂L₁)(H₂O)]SO₄ · H₂O, [Zn(H₂L₁)(H₂O)]SO₄ · H₂O, [Cu(H₂L₂)(H₂O)](OAc)₂, [Ni(H₂L₂)(H₂O)]SO₄ · H₂O, [Zn(H₂L₂)(H₂O)]SO₄ · 2H₂O, [Cu(H₂L₃)(H₂O)](OAc)₂ · H₂O, [Ni(H₂L₃)(H₂O)]SO₄ · 2H₂O, [Zn(H₂L₃)(H₂O)]SO₄ complexes were studied thermodynamically using the integral method applying the Coats–Redfern and Horowitz–Metzger equations and the thermodynamic parameters were calculated. It was found from the elemental analysis and the thermal studies, that the ligand behaves as tridentate ligand forming chelates with 1 : 1 (metal : ligand) stoichiometrically. The molar conductance measurements of the complexes in dimethyl sulfoxide solvent indicate that the complexes have an electrolytic nature. The biological activities of the three ligands in comparison with metal(II) complexes were studied against different Gram positive and Gram negative bacteria.     

Toxicity of metals to tadpoles of the common Sunda toad,Duttaphrynus melanostictus

Tadpoles of the common freshwater Sunda toad, Duttaphrynus melanostictus (Amphibia, Bufonidae), were exposed for a 4-day period under laboratory conditions to copper (Cu), cadmium (Cd), zinc (Zn), lead (Pb), nickel (Ni), iron (Fe), aluminum (Al), and manganese (Mn) at various concentrations. Mortality was assessed and median times of death (LT₅₀) and lethal concentrations (LC₅₀) were calculated. LT₅₀ and LC₅₀ increased with the decrease in mean exposure times and concentrations for all metals. LC₅₀ (96?h) for Cu, Cd, Zn, Pb, Ni, Fe, Al, and Mn were 0.03, 0.3, 4.2, 1.5, 8.8, 0.4, 1.9, and 39?mg?L^?1, respectively. Cu was the most toxic to D. melanostictus, followed by Cd, Fe, Al, Pb, Zn, Ni, and Mn (Cu?>?Cd?>?Fe?>?Al?>?Pb?>?Zn?>?Ni?>?Mn). Duttaphrynus melanostictus is similarly sensitive to these metals as other amphibian tadpoles.     

Biosorption of cadmium and nickel ions using marine macrophyte,Cymodocea nodosa

ABSTRACT

Seagrass (Cymodocea nodosa) ability to remove cadmium and nickel ions from single metal solutions was investigated in the present study. Metal ions were measured in the solution using an atomic absorption spectrophotometer. Various operational parameters (initial pH, biomass dose, metal ion concentration, and contact time) were tested and found to affect the uptake capacity of Cd (II) and Ni (II). More than 70% of biosorption capacity occurred in the first few minutes for both metal ions. The pseudo-second-order kinetic model and the Langmuir model were found to best fit the experimental data of Cd (II) and Ni (II) biosorption. The maximum uptake capacity (q_max) was 11.6 and 16.7?mg.g^?1 for Cd (II) and Ni (II), respectively. The biosorbent was characterised using Fourier transform infrared spectrometry (FTIR), scanning electron microscope (SEM), and energy-dispersive X-ray spectroscopy (EDX). The infrared spectrum demonstrated that hydroxyl, carboxyl, and phenolic functional groups are the major binding sites for Cd (II) and Ni (II) metals. The ion exchange mechanism plays an important role during biosorption process as shown in EDX analysis. Our results conclude that marine macrophyte C. nodosa can be used as a low-cost biosorbent for the removal of Cd (II) and Ni (II) in wastewater.     

Metal accumulation in sediment,water, and freshwater fish in a Dam Lake

Metal concentrations were determined in water, sediment, and freshwater fish samples (Squalus cephalus, Barbus esocinus, and Barbus xanthopterus) collected from Karakaya Dam Lake, Turkey, to estimate the risk of human consumption and pollution. Metal concentrations differed between the species (p??Zn?=?Cu in water and Fe?>?Zn?>?Mn?>?Ni?>?Cu in sediment. In general, the accumulation order of elements in the tissues all of the species sampled were found as Fe?>?Zn?>?Se?>?Mn?>?Cu?>?Ni?>?Cd in muscle, Zn?>?Fe?>?Mn?>?Se?>?Cu?>?Ni?>?Cd in gills, Fe?>?Zn?>?Se?>?Mn?>?Cu?>?Ni?>?Cd in liver and gonad, and Zn?>?Fe?>?Cu?>?Mn?>?Se?>?Ni?>?Cd in kidney. It was concluded that the fish from the dam lake are not heavily burdened with metals, but they should be controlled periodically to avoid excessive intake of trace metals by humans, and to monitoring the pollution of aquatic environment.     

Metal partitioning in sediment pore water from the Ondo coastal region,Nigeria

Distribution and equilibrium partitioning of metals (Cd, Cu, Cr, Fe, Ni, Pb, Mn, and Zn) between pore water and surface sediments at the Ilaje coast of Ondo State, Nigeria, were studied. The Ilaje River can be one of the interesting research locations because of its economic nature and history of oil pollution. Seasonal variations were observed to investigate possible variations in the availability of metals for organisms throughout the year. The concentrations in both sediments and pore water during the dry and wet seasons were as follows: Cu?>?Fe???Mn?>?Pb?>?Ni?>?Cr?>?Cd?>?Zn. The pore water–sediment partition coefficient (K _p) showed that Zn and Cd were highly mobile while Fe and Cu have restricted mobility. Dissolved organic carbon (DOC) in pore water had a strong influence on mobility and bioavailability of all the metals (p?K _oc), increased levels of Fe and Cu were linked to lithological origin. Concentrations of Pb and Ni were associated with petroleum-related sources. The significance of the field-based techniques for ecotoxicological purposes is discussed.     

Characteristics,sources and health risk assessment of toxic heavy metals in PM<Subscript>2.5</Subscript> at a megacity of southwest China

Twenty trace elements in fine particulate matters (i.e., PM_2.5) at urban Chengdu, a southwest megacity of China, were determined to study the characteristics, sources and human health risk of particulate toxic heavy metals. This work mainly focused on eight toxic heavy metal elements (As, Cd, Cr, Cu, Mn, Ni, Pb and Zn). The average concentration of PM_2.5 was 165.1 ± 84.7 µg m^?3 during the study period, significantly exceeding the National Ambient Air Quality Standard (35 µg m^?3 in annual average). The particulate heavy metal pollution was very serious in which Cd and As concentrations in PM_2.5 significantly surpassed the WHO standard. The enrichment factor values of heavy metals were typically higher than 10, suggesting that they were mainly influenced by anthropogenic sources. More specifically, the Cr, Mn and Ni were slightly enriched, Cu was highly enriched, while As, Cd, Pb and Zn were severely enriched. The results of correlation analysis showed that Cd may come from metallurgy and mechanical manufacturing emissions, and the other metals were predominately influenced by traffic emissions and coal combustion. The results of health risk assessment indicated that As, Mn and Cd would pose a significant non-carcinogenic health risk to both children and adults, while Cr would cause carcinogenic risk. Other toxic heavy metals were within a safe level.     

Synthesis,structural characterization and antimicrobial activity of nickel(II) tetrathiocyanato dicuperate(I) complexes with some acyl hydrazones

Heterobimetallic complexes of the type Ni[Cu(SCN)₂]₂ · L (where L = acetophenone benzoylhydrazone, acetophenone isonicotinoyl hydrazone, acetophenone salicyloylhydrazone (ash), acetophenone anthraniloylhydrazone, p-hydroxy acetophenone benzoylhydrazone, p-hydroxy acetophenone isonicotinoyl hydrazone p-hydroxy acetophenone salicyloylhydrazone (phash), p-hydroxy acetophenone anthraniloyl hydrazone), were synthesized and characterized. The complexes are polymeric, insoluble in common organic solvents and are nonelectrolytes. Magnetic moments and electronic spectral studies suggest a spin-free octahedral geometry for the complexes. IR spectra show the bidentate nature of all the ligands bonding through >C=O and >C=N–groups. The SCN group acts as a bridge between two metal centers. X-ray powder diffraction parameters for Ni[Cu(SCN)₂]₂ · ash and Ni[Cu(SCN)₂]₂ · phash correspond to orthorhombic and tetrahedral crystal lattices, respectively, for these complexes. The complexes show a significant antifungal activity against Rizoctonia, Stemphylium and Aspergillus sp. and antibacterial activity against Clostridium and Pseudomonas sp. The metal complexes are more active than the ligands.     

Effect of acid rain on the fractionation of heavy metals and major elements in contaminated soils

Acid rain is a serious environmental problem worldwide. In the present study, we investigated the effect of acid rain (1:1 equivalent basis H₂SO₄:HNO₃) at pH values of 2.0, 4.0 and 7.0 on the fractionation of heavy metals (Cd, Cu, Fe, Mn, Ni, Pb and Zn) and major elements (K, Na, Ca, and Mg) in contaminated calcareous soils over a 2084 h period. Heavy metals and major elements in soil samples were fractionated before and after 2084 h kinetic release using a sequential extraction procedure. Before kinetic studies the predominant fractions of K, Na, Ca, Mg, Cd and Ni were mainly associated with carbonate fraction (CARB), whereas Fe, Mn and Zn were associated with the Fe–Mn oxide fraction (Fe–Mn oxide). The highest percentage of Pb and Cu were found in the exchangeable (EXC) and organic matter (OM) fractions, respectively. After kinetic study using different simulated acid rain solutions, the major fractions of heavy metals (expect of Cu) and Na was the same as before release. Upon the application of different acid rain solutions, K and Mg were found dominantly in Fe–Mn oxide fraction, whereas Ca was in the EXC fraction. The results provide valuable information regarding metal mobility and indicated that speciation of metals (Cu and Zn) and major elements in contaminated calcareous soils can be affected by acid rain.     

Preparation,characterization and toxic activity of oxovanadium(IV) mixed-ligand complexes

New oxovanadium(IV) mixed-ligand complexes of the general composition [VO(L)(A)], where KHL?=?potassium salt of salicylideneglycine, A¹?=?bis(benzylidene)ethylenediamine, A²?=?bis (acetophenone)ethylenediamine, A³?=?di(2-pyridyl)amine, A⁴?=?bis(benzylidene)-1,8-diaminonaphthalene, A⁵?=?thiophene-o-carboxaldene-aniline, A⁶?=?thiophene-o-carboxaldene-p-anisidine, have been synthesized by the interaction of these ligands with vanadyl sulphate. The mixed-ligand complexes have been characterized on the basis of elemental analysis, magnetic measurements, electronic and infrared spectra. An octahedral structure has tentatively been assigned to all of the mixed-ligand complexes. The mixed-ligand complexes show higher toxic activity against the Salmonella typhi, Escherichia coli and Serratia mercescen as compared to the ligands, vanadyl sulphate and control (dimethyl sulphoxide). The mixed-ligand complexes were also tested against a standard drug (tetracycline).     

Cluster analysis of inorganic elements in particulate matter in the air environment of an equatorial urban coastal location

Concentrations of nine inorganic elements (Na, Zn, Ca, Fe, Ni, Mn, Cu, Cd and Al) in particulate matter (PM₁₀) in the air of an equatorial urban coastal location during 2009 were studied during summer and winter monsoon seasons using high-volume sampling techniques. Atomic absorption spectrophotometry was used to analyse the samples. The concentrations of most inorganic elements were higher during summer than winter, except for Cu and Zn. The main inorganic elements in PM₁₀ are Na, Zn and Ca. High concentrations of Na and Ca are due to marine aerosols. Analysis of enrichment factors showed that inorganic elements are from non-crustal sources. Cluster analysis identified five clusters in the summer and six in the winter: (1) PM₁₀–Ni, (2) Zn–Na, (3) Fe–Cu–Ca–Cd, (4) Mn and (5) Al for summer; and (1) PM₁₀, (2) Zn, (3) Fe–Ni, (4) Cu–Ca–Na–Cd, (5) Mn and (6) Al for winter. Combining both correlation and cluster analysis, it was found that Fe–Cu–Cd was from industry/vehicle emissions, Zn was from resuspended soil, Mn was from metallurgical processes, Ni was from a nearby power plant and Al was from crustal sources. Inorganic element concentrations could be a good indicator of local sources of PM₁₀.     

Bioconcentration of Cd and Ni in various tissues of two marine bivalves living in different habitats and exposed to heavily polluted seawater

Two marine bivalves, Mytilus galloprovincialis and Callista chione, were exposed to various concentrations of cadmium and nickel (0.5, 1.0, 2.5 and 20 ppm), for 20 days, plus 10 days’ depuration period, in a laboratory experiment. Animals from each experimental condition were dissected and the bioaccumulation and distribution of Cd and Ni were determined in their gills, mantles and remaining bodies. The concentrations of Fe and Zn were also measured. Heavy metal tolerance, bioconcentration and distribution of heavy metals in tissues were considerably different in M. galloprovincialis and C. chione: (i) both animals were tolerant to Ni pollution, even at the highest concentration used; (ii) C. chione was more tolerant to Cd; (iii) M. galloprovincialis was a better Cd and Ni accumulator, with the exception of the highest Cd concentration tested, where C. chione accumulated more Cd; (iv) Fe and Zn levels were much more affected in M. galloprovincialis; (v) in general, accumulation and distribution of Ni and Cd in the tissues were metal-, species- and time of exposure- dependent; (vi) significant amounts of heavy metals remained in the tissues after 10 days’ depuration. Our results support a hypothesis for a two competing processes mechanism for metal accumulation and detoxification.     

The potential ecological risk of soil trace metals following over five decades of agronomical practices in a semi-arid environment

The concentration and potential ecological risk of Mn, Zn, Cu, and Cd in the surface soils (0–30?cm) belonging to 12 soil profiles and 4 soil types (Vertisols, Chernozems, Calcisols, and Cambisols) from the cultivated soils and the corresponding uncultivated soils were investigated. Long-term cultivation caused a considerable build-up diethylene-triamine pentaacetic acid (DTPA)-extractable Mn (7–55%), and Cd (12–31%) as well as the total form of Zn (3–14%), Cu (8–25%), and Cd (33–78%) in all soil types. Following long-time cropping, total Zn (mean?=?73?mg?kg^?1), Cu (mean?=?33?mg?kg^?1), and Cd (mean?=?3.14?mg?kg^?1) and DTPA Zn (mean?=?1.2?mg?kg^?1) and Cu (mean?=?2.44?mg?kg^?1) were below their maximum allowable limits. However, the average amount of DTPA Cd in the tilled soils (min?=?0.4, max?=?0.75, mean?=?0.55?mg?kg^?1) was above its maximum permissible limit mainly due to the over application of phosphate fertilisers and the pesticides. Considering the potential ecological risk (RI) assessment of the cultivated soils (min?=?44, max?=?70, mean?=?54), the soil types were categorised as low (RI?≤?50) to moderate (50?相似文献   

Plants growing in a mining area: screening for metal accumulator plants possibly useful for bioremediation

A field study was conducted in an iron mine in Hamedan (Iran) to find native accumulator plants and to evaluate the extent of metal bioaccumulation in the naturally growing vegetation. The concentrations of total As, Cd, Cr, Fe, Mn, Mo, Ni, Pb, Si, and Zn were found to be higher in the mine than in soil. These plants accumulated the highest amounts of the following metals in their roots: Euphorbia cheiradenia As, Stipa barbata Cd, Pb and Cr, Euphorbia macroclada Cu, Centaurea iberica Fe, Reseda lutea Mo, Salvia spinosa Ni and Zn, and Xanthium strumarium Se. In the aerial parts, the highest metal accumulation was found in Epilobium fragilis As, Carthamus oxyacantha Cd, Fe, Mn, and Pb, Verbascum speciosum Cu, Centaurea iberica Mo, Salvia spinosa Ni and Cr, Glaucium grandiflorum Se, and Malva neglecta Zn. Enrichment factors and bioconcentration factors were also determined; C. oxyacantha, S. spinosa, M. neglecta, C. iberica, V. speciosum, G. grandiflorum, and E. fragilis are the most effective accumulators and are proposed for phytoremediation of polluted soils.     

Metal remediation potential of naturally occurring plants growing on barren fly ash dumps

The present study aimed to elucidate the remediation potential of visibly dominant, naturally growing plants obtained from an early colonized fly ash dump near a coal-based thermal power station. The vegetation comprised of grasses like Saccharum spontaneum L., Cynodon dactylon (L.) Pers., herbs such as Tephrosia purpurea (L.) Pers., Sida rhombifolia L., Dysphania ambrosioides (L.) Mosyakin & Clemants, Chromolaena odorata (L.) King & H.E. Robins along with tree saplings Butea monosperma (Lam.) Taub. The growth of the vegetation improved the N and P content of the ash. Average metal concentrations (mg kg^?1) in the ash samples and plants were in order Mn (345.1)?>?Zn (63.7)?>?Ni (29.3)?>?Cu (16.8)?>?Cr (9.9)?>?Pb (1.7)?>?Cd (0.41) and Cr (58.58)?>?Zn (52.74)?>?Mn (39.09)?>?Cu (10.71)?>?Ni (7.45)?>?Pb (5.52)?>?Cd (0.14), respectively. The plants showed fly ash dump phytostabilization potential and accumulated Cr (80.19–178.11 mg kg^?1) above maximum allowable concentrations for plant tissues. Positive correlations were also obtained for metal concentration in plant roots versus fly ash. Saccharum spontaneum showed highest biomass and is the most efficient plant which can be used for the restoration of ash dumps.

     

The effects of alginate microspheres on phytoremediation and growth of Lemna minor in the presence of Cd

Today, the removal of increased amount of contaminant concentrations in nature such as metals, nanoparticles, has become an essential issue to struggle with. In this paper, both the toxic effects of non-essential Cd on Lemna minor in presence of alginate microspheres and metal removal capacity of Cd-exposed L. minor and microspheres were investigated. Three test groups were constructed: group (L) containing Lemna, group (M) containing alginate microsphere and group (L?+?M) containing alginate microsphere and Lemna. Five different levels of Cd concentrations were added into these groups. Estimation models were constructed to estimate Cd removal capacities of L. minor and microspheres, and time-concentration-dependent growth (GRC) rates of both microsphere-containing and non-containing groups were modelled by regression analysis. It was seen that microspheres alone only had no positive or negative effects on Lemna growth. It was observed that, for all test groups the time-dependent growth rate has both increase–decrease trends in general. The toxicity effect of Cd on Lemna growth was reduced by adding microspheres into medium. Furthermore, the results stated that test groups containing only microspheres (M, 0–97.56%) and consortium groups (M?+?L, 0–98.26%) were slightly more successful in Cd removal process compared to Lemna (L) groups (L, 0–97.32%).     

Determination of the levels of selected metals in seeds,flowers and fruits of medicinal plants used for tapeworm treatment in Ethiopia

The level of accumulation of selected essential and non-essential metals, namely; Ca, Cu, Fe, Zn, Mn, Cd, Pb, and Cr have been investigated in the seeds, fruits, and flowers of some medicinal plants utilized for tapeworm treatment in Ethiopia and their respective soil samples. These include seed of Cucurbita maxima (Duba), fruit of Embelia abyssinica (Ankoko), flowers of Hagenia abyssinica (Kosso), and fruits of Rosa abyssinica (Kega) and their respective soil samples. A wet digestion procedure with a mixture of conc. HNO₃ and HClO₄ for the plant samples and a mixture of conc. HNO₃, HCl, and H₂O₂ for soil samples were used to solubilize the metals. Ca (1280–12,670?mg?kg^?1) was the predominant metal followed by Fe (104–420?mg?kg^?1), and Zn (18–185?mg?kg^?1) in all the plant materials except for Hagenia abyssinica flower from Hirna in which Mn (16–42?mg?kg^?1) followed by Fe. Among the non-essential toxic metals, Pb was not detected in Cucurbita maxima of Boji, Gedo and Hirna origins and in Rosa abyssinica of Hirna site. Similarly, Cr was not detected in Rosa abyssinica fruits of Boji and Gedo sites. The sampled soils were found to be between strongly acidic to weakly basic (pH: 4.7–7.1). In the soil samples, Ca (8528–18,900?mg?kg^?1) was the most abundant metal followed by Fe (417–912?mg?kg^?1), Zn (155–588?mg?kg^?1), Mn (54–220?mg?kg^?1), Cr (21–105. mg?kg^?1), Cu (11–58?mg?kg^?1), Pb (13–32?mg?kg^?1) and Cd (2.8–4.8?mg?kg^?1). The levels of most of the metals determined in the medicinal plants and the respective soil samples are in good agreement with those reported in the literature and the standards set for the soil by various legislative authorities.     

Mechanism of toxicity of ionic copper and copper complexes to algae

The mechanism of toxicity of ionic copper and copper complexes to growth, photosynthesis, respiration, ATP levels and mitochondrial electron-transport chain-activity in two marine diatoms, Nitzschia closterium (Ehrenberg) W. Smith (Hasle, 1964) and Asterionella glacialis Castracane, and one freshwater green alga, Chlorella pyrenoidosa Chick was investigated. Copper ions depressed both cell division and photosynthesis in A. glacialis and C. pyrenoidosa, whereas ionic copper concentrations which were inhibitory to cell division in N. closterium had no effect on photosynthesis, respiration, ATP production, electron transport or membrane ultrastructure. This suggests that in N. closterium, copper does not act on the chloroplast, the mitochondrion, or the cell membrane, since if it did, the above parameters should be affected. Copper-ethylxanthogenate was exceptional amongst the copper complexes in that it stimulated respiration, mitochondrial electrontransport and ATP formation in N. closterium under conditions of strongly inhibited cell division and slightly stimulated photosynthesis. Ionic copper toxicity may result from an intracellular reaction between copper and reduced glutathione (GSH), leading to a lowering of the GSH:GSSG ratio and suppression of mitosis. In addition, copper inhibits the enzyme catalase and reduces cell defence mechanisms against H₂O₂ and oxygen-free radicals. Lipid-soluble copper complexes are more toxic than ionic copper because both the metal and the ligand are introduced into the cell. Toxicity of ionic copper is ameliorated by trivalent metal ions in the growth medium, including those of Mn, Co, Al, Fe and Cr which form a layer of metal (III) hydroxide around the algal cell, adsorb copper and reduce its penetration into the cell. The degree of insolubility of the metal (III) hydroxide is related to its ability to protect against copper toxicity. In addition, manganese and cobalt catalytically scavenge damaging H₂O₂ and superoxide radicals, respectively, produced by the cell.     

Differential effects of UV-B radiation fluence rates on growth,photosynthesis, and phosphate metabolism in two cyanobacteria under copper toxicity

This work was undertaken to ascertain the impact of different fluence rates of ultraviolet-B (UV-B) radiation on two cyanobacterial biofertilizers, Phormidium foveolarum and Nostoc muscorum, growing under copper toxicity. Copper (2 and 5?µmol?L^?1) and high UV-B fluence rate (UV-B_H; 1.0?µmol?m^?2?s^?1) decreased the growth, pigment content, photosynthetic oxygen yield, phosphate uptake, and acid phosphatase activity in both the strains analyzed after 24 and 72?h of experiments, and combined exposure further enhanced the toxic effects. Respiration and alkaline phosphatase activities were stimulated appreciably. The damaging effect was shown on the order on pigments: phycocyanin?>?chlorophyll a?>?carotenoids, and on photosystems: whole chain photosynthetic reaction?>?photosystem II?>?photosystem I. Partial recovery in the photosystem II activity in the presence of artificial electron donors; diphenyl carbazide (DPC), hydroxylamine (NH₂OH), and manganese chloride (MnCl₂) pointed out the interruption of electron flow on the oxidation side of photosystem II. Unlike UV-B_H, low UV-B fluence rate (UV-B_L; 0.1?µmol?m^?2?s^?1), rather than causing damaging effect partially, alleviated the toxic effects of Cu. This study suggests that the cyanobacterium P. foveolarum is less sensitive against UV-B_H and excess Cu (2 and 5?µmol?L^?1), thus P. foveolarum may be used as a biofertilizer for sustainable agriculture.