Spectrophotometric determination of platinum(IV) in alloys, complexes, environmental, and pharmaceutical samples using 4-[N,N-(diethyl)amino] benzaldehyde thiosemicarbazone

4-[N,N-(Diethyl)amino] benzaldehyde thiosemicarbazone (DEABT) is proposed as an analytical reagent for the spectrophotometric determination of platinum(IV). The DEABT forms 1:2 yellow complex with Pt(IV), which is sparingly soluble in water and completely soluble in water–ethanol–DMF medium. The Pt(IV)–DEABT complex shows maximum absorbance at 405 nm. Beer’s law is valid up to 7.80 μg cm^???3, and optimum concentration range for the determination of platinum(IV) is 0.48–7.02 μg cm^???3. The molar absorptivity and Sandell’s sensitivity of the method are found to be 1.755 × 10⁴ dm³ mol^???1 cm^???1 and 0.0012 μg cm^???2, respectively. The relative error and coefficient of variation (n?=?6) for the method does not exceed ±0.43% and 0.35%, respectively. Since the method tolerates a number of metal ions commonly associated with platinum, it can be employed for the determination of platinum in environmental samples, pharmaceutical samples, alloys, catalysts, and complexes. The method is rapid as the Pt(IV)–DEABT complex is soluble in water–ethanol–DMF medium and not requiring any time consuming extraction method for the complex.     

Voltammetric trace determination of mercury using plant refuse modified carbon paste electrodes

Citrus limon peel (kitchen waste) and Leucaena leucocephala seeds (agricultural waste) were used as a modifier for fabrication of modified carbon paste electrode for determination of mercury in aqueous sample using differential pulse anodic stripping voltammetry. Mercury was adsorbed on electrode surface at open circuit and anodic stripping voltammetric scan was run from ?0.5 to 0.5 V. Various electrochemical parameters including amount of modifier, supporting electrolyte, accumulating solvent, pH of the accumulating solvent, and accumulation time were investigated. The effect of presence of other metal ions and surfactants was also studied. In comparison C. limon peel proved to be a better modifier than L. leucocephala seed biomass. This was justified by electrode characterization using cyclic voltammetry that indicated decrease in resistance of electrode when C. limon peel was used as modifier and increase when modifier was L. leucocephala seeds. Maximum current response was obtained using 5 % C. limon peel biomass, hydrochloric acid as supporting electrolyte, acetate buffer of pH 6 as an accumulating solvent, 10-min accumulation time, and scan rate of 50 mV/s. Linear calibration curves were obtained in the concentration range 100 to 1,000 μg L^?1 of mercury for accumulation time of 10 min with limit of detection of 57.75 μg L^?1 and limit of quantification of 192.48 μg L^?1. This technique does not use mercury as electrode material and, therefore, has a positive environmental benefit.     

The high potential of Pelargonium roseum plant for phytoremediation of heavy metals

The major objective of this investigation was to evaluate the potential of scented geraniums, Pelargonium roseum, to uptake and accumulate heavy metals nickel (Ni), cadmium (Cd), or lead (Pb). For this, plants were grown in an artificial soil system and exposed to a range of metal concentrations over a 14-day treatment period. Then, metals from the entire biomass were extracted. The results showed that scented geranium plants accumulated in excess of 20,055 mg of Ni kg^?1 dry weight (DW) of root and 10,889 mg of Ni kg^?1 DW of shoot, and in excess of 86,566 mg of Pb kg^?1 DW for roots and 4,416 mg of Pb kg^?1 DW for shoots within 14 days. Also, the uptake and accumulation of cadmium in roots of scented geranium plants increased with the exposure at low (250, 500 mg?L^?1) and medium level (750 mg?L^?1) followed by a decline at the highest level (1,000 mg?L^?1). The highest accumulation in roots (31,267 mg?kg^?1 DW) was observed in 750 mg?L^?1 cadmium treatment. In the shoots of scented geraniums, the highest amount of metal accumulation (1,957 mg?kg^?1 DW) was detected at 750 and 1,000 mg?L^?1 of cadmium in the culture solution. Finally, since the high concentrations of Ni or Pb accumulated in shoots of scented geranium has far exceeded 0.1 % DW and for Cd has far exceeded 0.01 % DW, P. roseum is a new hyperaccumulator species for these metals and can be used in phytoremediation industry.     

Simultaneous quantification of Bi(III) and U(VI) in environmental water samples with a complicated matrix containing organic compounds

Trace amounts of bismuth(III) and uranium(VI) can be simultaneously determined in a single scan by adsorptive cathodic stripping voltammetry in the presence of cupferron as a complexing agent. Optimal conditions were found to be: 0.1 mol?L^?1 acetate buffer (pH 5.3), 5?×?10^?5?mol?L^?1 cupferron, accumulation potential of ?0.25 V, and accumulation time of 30 s. The linear range of Bi(III) and U(VI) was observed over the concentration range from 2?×?10^?9 to 2?×?10^?7?mol?L^?1 and from 1?×?10^?8 to 5?×?10^?7?mol?L^?1, respectively. The influence of the main components of real water samples such as foreign ions and organic substances (surface active substances, humic substances) was precisely investigated. The method was applied to the simultaneous measurements of bismuth and uranium in natural water samples.     

Application of zirconium–iridium permanent modifier for the simultaneous determination of lead, cadmium, arsenic, and nickel in atmospheric particulate matter by multi-element electrothermal atomic absorption spectrometry

A novel and robust method for the simultaneous determination of lead, cadmium, arsenic, and nickel in atmospheric particulate matter by multi-element electrothermal atomic absorption spectrometry was developed, using zirconium–iridium coating as permanent modifier (140 μg Zr and 4 μg Ir). After 300 atomization cycles, it was necessary to add 2 μg of Ir. Due to the varying concentrations of Pb in atmospheric particulate matter, lead was monitored at two wavelengths, at the less sensitive line of 261.4 nm for high concentration samples (>20 μg?L^?1) or at 283.3 nm for the low concentration samples. Matrix-matched calibration had to be performed for quantitative recoveries (96–102 %). Following this approach, the four elements were determined in atmospheric particulate matter samples from an industrial area near the city of Athens in two different time periods (cold–warm) with limits of detection of 5.5 ng?m^?3 for Pb at 261.4 nm and 0.29 ng?m^?3 at 283.3 nm, 0.019 ng?m^?3 for Cd, 0.14 ng?m^?3 for As, and 0.22 ng?m^?3 for Ni. Lead, Cd, and As levels were very low, whereas Ni content was at comparable levels with other areas worldwide.     

Application of cold-induced aggregation microextraction as a fast,simple, and organic solvent-free method for the separation and preconcentration of Se(IV) in rice and various water samples

The developed method is based on cold-induced aggregation microextraction of Se(IV) using the 1-butyl-3-methylimidazolium hexafluorophosphate ionic liquid as an extractant followed by spectrophotometry determination. The extraction of Se(IV) was performed in the presence of dithizone as the complexing agent. In this method, a very small amount of 1-butyl-3-methylimidazolium hexafluorophosphate was added to the sample solution containing Se-dithizone complex. Then, the solution was kept in a thermostated bath at 50 °C for 4 min. Subsequently, the solution was cooled in an ice bath and a cloudy solution was formed. After centrifuging, the extractant phase was analyzed using a spectrophotometric detection method. Some important parameters that might affect the extraction efficiency were optimized (HCl, 0.6 mol L^?1; dithizone, 4.0?×?10^?6 mol L^?1; ionic liquid, 100 μL). Under the optimum conditions, good linear relationship, sensitivity, and reproducibility were obtained. The limit of detection (LOD) (3S_b/m) was 1.5 μg L^?1, and the relative standard deviation (RSD) was 1.2 % for 30 μg L^?1 of Se(IV). The linear range was obtained in the range of 5–60 μg L^?1. It was satisfactory to analyze rice and various water samples.     

Hazard assessment of metals in invasive fish species of the Yamuna River,India in relation to bioaccumulation factor and exposure concentration for human health implications

Monitoring of heavy metals was conducted in the Yamuna River considering bioaccumulation factor, exposure concentration, and human health implications which showed contamination levels of copper (Cu), lead (Pb), nickel (Ni), and chromium (Cr) and their dispersion patterns along the river. Largest concentration of Pb in river water was 392 μg L^?1; Cu was 392 μg L^?1 at the extreme downstream, Allahabad and Ni was 146 μg L^?1 at midstream, Agra. Largest concentration of Cu was 617 μg kg^?1, Ni 1,621 μg kg^?1 at midstream while Pb was 1,214 μg kg^?1 at Allahabad in surface sediment. The bioconcentration of Cu, Pb, Ni, and Cr was observed where the largest accumulation of Pb was 2.29 μg kg^?1 in Oreochromis niloticus and 1.55 μg kg^?1 in Cyprinus carpio invaded at Allahabad while largest concentration of Ni was 174 μg kg^?1 in O. niloticus and 124 μg kg^?1 in C. carpio in the midstream of the river. The calculated values of hazard index (HI) for Pb was found more than one which indicated human health concern. Carcinogenic risk value for Ni was again high i.e., 17.02?×?10^?4 which was larger than all other metals studied. The results of this study indicated bioconcentration in fish due to their exposures to heavy metals from different routes which had human health risk implications. Thus, regular environmental monitoring of heavy metal contamination in fish is advocated for assessing food safety since health risk may be associated with the consumption of fish contaminated through exposure to a degraded environment.     

Validation of spectrophotometric method for Se(IV) determination: analytical applications

As selenium is an important part of the antioxidant enzymes and also because there are several studies suggesting a possible link between cancer and selenium deficiency, this paper presents a spectrophotometric method for the assay of Se(IV), using N,N-diethyl-p-phenylenediamine monohydrochloride as reagent. The proposed method is based on the reaction between the selenium and potassium iodide in low acidic medium, when iodine is released. This last product will further oxidise the new reagent. The final obtained product is strongly coloured in red and has an absorption maximum at 552 nm and molar extinction coefficient (ε) of 6.1?×?10⁴ L mol^?1 cm^?1. The optimum working conditions were established, and the developed method was validated, being characterised by a good linearity (in the range of 0.5–3.0 μg/mL), a limit of detection (0.0573 μg/mL) and a limit of quantification (0.1737 μg/mL). At the same time, the repeatability, the precision of the method and the accuracy were established. The proposed and validated method was applied with good results for the determination of Se(IV) in spring and bottled water from Iasi and also in pharmaceutical and cosmetic products.     

The use of silica gel modified with allyl 6-methyl-4-phenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate for selective separation and preconcentration of lead in environmental samples

The aim of the present work is the assessment of a new sorbent, prepared using silica gel coated with a pyrimidine derivative (allyl 6-methyl-4-phenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate), for extraction and preconcentration trace amount of lead from different samples prior to determination by flame atomic absorption spectrometry. Common coexisting ions did not interfere with the separation and determination of lead at pH?6, so that lead ion completely adsorbed on the column. The limit of detection based on three times the standard deviation of the blank was found to be 0.53 ng?mL^?1 in original solution. Obtained sorption capacity for 1 g sorbent was 5.0 mg Pb. The linearity was maintained in the concentration range of 0.1–30.0 ng?mL^?1 for the concentrated solution. Eight replicate determinations of 2.0 μg?mL^?1 of lead in the final solution gave relative standard deviation of ±2.6 %. The proposed method was successfully applied to the determination trace amounts of lead in the environmental samples such as carrot, rice, zardchoobe, and real water samples.     

Differential pulse adsorptive stripping voltammetric determination of simeton in its formulations and vegetables

A sensitive adsorptive stripping voltammetric method for the determination of simeton with universal buffer solution has been described. The method was based on the adsorption accumulation of simeton at a hanging mercury drop electrode. The overall reduction process is under controlled diffusion. The adsorptive peak was observed at ?0.8 V vs SCE in acidic solution 2 < pH < 6. The peak response was characterized with respect to pH, accumulation potential, time, and scan rate. The calibration plot was found to be linear from 1.13 × 10^???5 to 3.5 × 10^???8 M with a limit of detection of 2.0 × 10^???8 M. Finally, the method has been applied for the determination of simeton in its formulations and vegetable samples.     

Biological endpoints, enzyme activities, and blood cell parameters in two anuran tadpole species in rice agroecosystems of mid-eastern Argentina

Different biological variables of tadpoles, including survival, development and growth rates, and biomarkers [cholinesterases, glutathione-S-transferases (GST), and blood cell morphology] were evaluated in two anuran species, Scinax squalirostris (Hylidae) and Leptodactylus mystacinus (Leptodactylidae), using in situ experimental chambers in a rice field (RF) sprayed with insecticide Lambda-cyhalothrin (LTC) by aircraft in Santa Fe Province, Argentina. We found a significant decrease in body weight (0.62?±?0.04 g) of L. mystacinus and an increased development rate of S. squalirostris in individuals from RF (41?±?1; Gosner) with respect to individuals from the reference site (RS: 0.93?±?0.04 g and 37?±?0; respectively). In S. squalirostris, individuals from RF mean values of butyrylcholinesterase activities decreased at 48 (4.09?±?0.32 nmol min^-1 mg^-1 of TP) and 96 h (3.74?±?0.20 nmol min^-1 mg^-1 of TP), whereas inhibition of acetylcholinesterase was observed at 96 h (47.44?±?2.78 nmol min^-1 mg^-1 of TP). In L. mystacinus from RF, an induction of acetylcholinesterase activity was observed at 96 h (36.01?±?1.09 nmol min^-1 mg^-1 of TP). Glutathione-S-transferase levels varied between species, being higher in L. mystacinus individuals but lower in S. squalirostris from RF at 48 (272.29 ±11.78 and 71.87?±?1.70 nmol min^-1 mg^-1 of TP; respectively) and 96 h (279.25?±?13.06 and 57.62?±?4.58 nmol min^-1 mg^-1 of TP, respectively). Blood cell parameters revealed a lower number of mitotic cells (MC: 0.36?±?0.31%o for S. squalirostris and 0.08?±?0.05 %o for L. mystacinus) and higher number of eosinophils (E: 3.45?±?1.75 %o for S. squalirostris and 7.64?±?0.98 %o for L. mystacinus) in individuals from the RF than in individuals from the RS (MC: 2.55?±?0.74 %o for S. squalirostris and 1.87?±?0.72%o for L. mystacinus; and E: 0.13?±?0.09 for S. squalirostris and 3.20?±?0.80 for L. mystacinus). Overall, our results demonstrate the existence of apparent differences in sensitivity between species in a series of sublethal responses to short-term exposure in RF after the application of Lambda-cyhalothrin. We suggest that the integral use of biological endpoints (development and growth) together with biomarkers (cholinesterase, GST, and blood cell parameters) may be a promising integral procedure for investigating pesticide exposure in wild frog populations.     

Dissipation kinetics and assessment of processing factor for chlorpyrifos and lambda-cyhalothrin in cardamom

The dissipation kinetics and method for estimation of residues of chlorpyrifos and lambda-cyhalothrin in cardamom were studied and developed. The limit of detection and limit of quantitation arrived for the compounds were 0.01 and 0.025 μg?g^?1, respectively. Gas chromatographic response of chlorpyrifos and lambda-cyhalothrin residues was linear in the range of 0.01–0.50 μg?g^?1 and the mean recovery obtained was 97.3 % for chlorpyrifos and 98.9 % for lambda-cyhalothrin with satisfactory relative standard deviation values. The mean initial residues of chlorpyrifos applied at a concentration of 0.05 % in cardamom was 2.5 μg?g^?1 and the residue was 8.1 μg?g^?1 after processing, with a processing factor of 3.24, while lambda-cyhalothrin when applied at 0.0025 % resulted in initial residues of 1.63 μg?g^?1 that magnified to 4.86 μg?g^?1 on curing, with a processing factor of 2.98. The half-life of chlorpyrifos was in the range of 5.1–5.24 days while that of lambda-cyhalothrin was in the range of 4.40–4.55 days. The processing factor arrived at in the above experiment lead to the conclusion that the residues of chlorpyrifos got magnified to 3.24–3.68 times and that of lambda-cyhalothrin got magnified to 2.98–3.46 times of initial residues, consequent to loss of weight due to dehydration during curing.     

New kinetic-spectrophotometric method for monitoring the concentration of iodine in river and city water samples

A new kinetic method has been developed for the determination of iodine in water samples. The method is based on the catalytic effect of I^? with the oxidation of Indigo Carmine (IC) by KBrO₃ in the sulfuric acid medium. The optimum conditions obtained are 0.16 M sulfuric acid, 1?×?10^?3 M of IC, 1?×?10^?2 M KBrO₃, reaction temperature of 35°C, and reaction time of 80 s at 612 nm. Under the optimized conditions, the method allowed the quantification of I^? in a range of 12–375 ng/mL with a detection limit of 0.46 ng/mL. The method was applied to the determination of iodine in river and city water samples with the satisfactorily results.     

Persistence of metaflumizone on cabbage (Brassica oleracea Linne) and soil, and its risk assessment

Metaflumizone is a novel sodium channel blocker insecticide of semicarbazone class. It provides good to excellent control of most of the economically important lepidopterous pests and certain pests in the orders Coleoptera, Hemiptera, Hymenoptera, Diptera, Isoptera, and Siphonaptera. Although metaflumizone has been marketed globally for several years and got registered in India in the year 2009, specifically for the control of DBM on cabbage, to our knowledge, no food safety aspects of metaflumizone residue on cabbage have ever been reported in the literature in India or elsewhere. The present study was undertaken to evaluate the persistence of metaflumizone on cabbage and soil, vis-a-vis its risk assessment, following two spray applications of metaflumizone 220 SC (Verismo®), each at recommended and double dose of 200 and 400 g?a.i.?ha^?1 respectively. Initial residue deposits of metaflumizone on cabbage were 0.46 and 0.51 mg?kg^?1 at recommended and 0.76 and 0.85 mg?kg^?1 at double the recommended dose following the first spray and second spray application. The residues persisted beyond 5 days from both the treatments and dissipated with the half-life ranging from 1.7–2.1 days. Initial deposits of metaflumizone on soil ranged from 0.23–0.37 mg?kg^?1 and degraded with a half life ranging from 4.0–4.8 days. No degradation product of metaflumizone was detected in cabbage and soil at any point of time. Soil samples collected from the treated field after 7 days were free from any residue of metaflumizone or its metabolites. A pre-harvest waiting period of 3 days after application was suggested based on calculation of theoretical maximum daily intake.     

Plastic litter accumulation on high-water strandline of urban beaches in Mumbai, India

Today, almost every beach on every coastline is threatened by human activities. The inadequate recycling and poor management of waste in developing countries has resulted in considerable quantities of plastic contaminating beaches. Though India has long coastline of 5,420 km along the mainland with 43 % of sandy beaches, data on litter accumulation, particularly the plastics, which are one of the most common and persistent pollutants in marine environment, are scanty. The abundance and distribution of plastic litter was quantitatively assessed in four sandy beaches in Mumbai, India, bimonthly from May 2011 to March 2012. Triplicates of 2?×?2 m (4 m²) quadrats were sampled in each beach with a total of 72 quadrats. Overall, average abundance of 11.6 items m^?2 (0.25–282.5 items m^?2) and 3.24 g m^?2 (0.27–15.53 g m^?2) plastic litter was recorded in Mumbai beaches. Plastic litter accumulation significantly varied temporally and spatially at p?=?0.05. Significantly higher plastic litter accumulation was recorded in Juhu beach. Furthermore, the highest abundance by weight was recorded in November and May numerically. More than 80 % of plastic particles were within the size range of 5–100 mm both by number and weight. Moreover, coloured plastics were predominant with 67 % by number of items and 51 % by weight. Probably, the intense use of beaches for recreation, tourism, and religious activities has increased the potential for plastic contamination in urban beaches in Mumbai.     

Synthesis and characterization of zeolites prepared from industrial fly ash

In this paper, we present the possibility of using fly ash to produce synthetic zeolites. The synthesis class F fly ash from the Stalowa Wola SA heat and power plant was subjected to 24 h hydrothermal reaction with sodium hydroxide. Depending on the reaction conditions, three types of synthetic zeolites were formed: Na-X (20 g fly ash, 0.5 dm³ of 3 mol?·?dm^?3 NaOH, 75 °C), Na-P1 (20 g fly ash, 0.5 dm³ of 3 mol?·?dm^?3 NaOH, 95 °C), and sodalite (20 g fly ash, 0.8 dm³ of 5 mol?·?dm^?3 NaOH?+?0.4 dm³ of 3 mol?·?dm^?3 NaCl, 95 °C). As synthesized materials were characterized to obtain mineral composition (X-ray diffractometry, Scanning electron microscopy-energy dispersive spectrometry), adsorption properties (Brunauer-Emmett-Teller surface area, N₂ isotherm adsorption/desorption), and ion exchange capacity. The most effective reaction for zeolite preparation was when sodalite was formed and the quantitative content of zeolite from X-ray diffractometry was 90 wt%, compared with 70 wt% for the Na-X and 75 wt% for the Na-P1. Residues from each synthesis reaction were the following: mullite, quartz, and the remains of amorphous aluminosilicate glass. The best zeolitic material as characterized by highest specific surface area was Na-X at almost 166 m²?·?g^?1, while for the Na-P1 and sodalite it was 71 and 33 m²?·?g^?1, respectively. The ion exchange capacity decreased in the following order: Na-X at 1.8 meq?·?g^?1, Na-P1 at 0.72 meq?·?g^?1, and sodalite at 0.56 meq?·?g^?1. The resulting zeolites are competitive for commercially available materials and are used as ion exchangers in industrial wastewater and soil decontamination.     

Distributions, sources, and ecological risks of DDT-related contaminants in water, suspended particulate matter, and sediments from Haihe Plain, Northern China

The residual levels of dichlorodiphenyltrichloroethane (DDT) and its metabolites (DDXs, including p,p′-DDT, DDD, and DDE) in water, suspended particulate matter (SPM), and sediments from major rivers, lakes, and reservoirs in Haihe Plain were measured with a gas chromatograph equipped with a ⁶³Ni microelectron capture detector. In the fall of 2004, the contents of the total DDXs in the water and SPM were 0.29?±?0.69 ng L^?1 and 423.13?±?577.85 ng g^?1 dry wt., respectively. In the spring of 2005, the total DDXs were 0.36?±?0.91 ng L^?1 for water and 35.93?±?62.65 ng g^?1 dry wt. for SPM. The average concentration of DDXs for sediments was 7.10?±?7.57 ng g^?1 dry wt. during the two seasons. The Eastern-Hebei-Province Coastland River System was the most polluted, which was mainly attributable to the extensive use of DDT pesticide and dicofol in that system. Recent DDT inputs still occur in some regions, as indicated by DDT/(DDD + DDE) > 1 at 29–36 % of the sites for water and 55–61 % of the sites for SPM. The potential ecological risks of DDT in the water were assessed using a species sensitivity distribution model. Only shrimp and crabs were found to have potentially affected fraction values of 1.63?×?10^?3 to 2.27?×?10^?4, with probabilities beyond the hazardous concentration for 5 % of species (HC5) values of 1.90–2.56 %, suggesting only slight risks. DDXs in the sediments of some sites were also of potential risk to benthic organism based on consensus-based sediment quality guidelines.     

First study on anthropogenic Pt, Pd, and Rh levels in soils from major avenues of S?o Paulo City, Brazil

Over the last years, investigations on the increase of platinum (Pt), palladium (Pd), and rhodium (Rh) levels in urban environments of big cities all over the world - especially to catalytic converters emissions - have been grown up enormously. S?o Paulo City is the 6th largest megacity in the world having about 20 million inhabitants and an ever increasing seven million motor vehicle fleet. In spite of this, there has never been an investigation regarding Pt, Pd, and Rh levels in the city. In the present study, Pt, Pd, and Rh concentrations were determined in soils adjacent to seven main high-density traffic avenues in the metropolitan region of S?o Paulo City. Inductively coupled plasma mass spectrometry was employed - after ultrasound-assisted aqua regia leaching - as analytical technigue. The results showed concentration levels up to 378?ng?g^?1 for Pd, 208?ng?g^?1 for Pt, and 0.2 to 45?ng?g^?1 for Rh. These levels are much higher than those considered for the geochemical background of soils, indicating a catalytic converter source. Due to the different Pt/Pd/Rh ratio in Brazilian automobile catalytic converters, lower levels of Pt/Pd ratios compared with other similar studies were observed. The obtained results are the first data for monitoring Pt, Pd, and Rh pollution in S?o Paulo City soils.     

Bioaccumulation and toxicity of arsenic in cyanobacteria cultures separated from a eutrophic reservoir

The bioaccumulation and toxicity of arsenate (arsenic (As)(V)) was studied using three cultures of cyanobacterial species—Oscillatoria tenuisa, Anabaena affinis, and Microcystis aeruginosa—that were isolated from a eutrophic reservoir. The As(V) uptake depended on the cyanobacterial species, the growth phase of the cyanobacteria, the duration of exposure, and the initial concentration of As(V). The specific growth rates of the three cultures immediately following the logarithmic phase were 0.033–0.041 L/day when the initial concentration of As(V) was 50 mg/L. These rates were 2.3–3.6 times less than those in the original culture medium without As(V). The rate of intake of As(V) in the logarithmic phase cultures greatly exceeded that in the stationary cultures. The accumulation of As(V) by the three cultures increased rapidly within 1 week from the initial value of 3.23?×?10^?2–5.40?×?10^?2 to 5.06?×?10^?1–6.73?×?10^?1 ng/cell in the logarithmic phase. The effective concentrations (EC₅₀) of As(V) for inhibiting the growth of the three cyanobacterial species growth of at 72 h followed the order Oscillatoria tenuisa (3.8 mg/L)?>?A. affinis (2.6 mg/L)?>?M. aeruginosa (1.2 mg/L). The cyanobacterial species that was most sensitive to As(V) was M. aeruginosa. Preliminary results from SEM-map studies suggest most of the As(V) in Microcystis aeruginosa accumulated in the cytoplasm (intercellular), while in O. tenuisa and A. affinis, a large proportion of As(V) bound to the cell wall (extracellular). These differences were understood with reference to the variation among the metabolic properties and morphological characteristics of the cyanobacterial species.     

Assessment of physico-chemical qualities and heavy metal concentrations of Umgeni and Umdloti Rivers in Durban,South Africa

We assessed the effects of seasonal dynamics on the physico-chemical qualities and heavy metals concentrations of the Umgeni and Umdloti Rivers in Durban, South Africa. Water samples were taken from nine different sampling points and analysed for the following parameters; temperature, pH, turbidity, electrical conductivity (EC), biological oxygen demand (BOD₅), chemical oxygen demand (COD), phosphate (PO₄ ^2?), nitrate (NO₃ ^2?), ammonium (NH₄ ⁺), sulphate (SO₄ ^2?), lead (Pb²⁺), mercury (Hg²⁺), cadmium (Cd²⁺), aluminium (Al³⁺), and copper (Cu²⁺) using standard methods. The data showed variations it terms of the seasonal fluctuations and sampling regime as follows: temperature 12–26.5 °C; pH 5.96–8.45; turbidity 0.53–18.8 NTU; EC 15.8–5180 mS m^?1; BOD₅ 0.60–7.32 mg L^?1; COD 10.5–72.9 mg L^?1; PO₄ ^2??<?500–2,460 μg L^?1; NO₃ ^2? <0.05–4.21 mg L^?1; NH₄ ⁺?<?0.5–1.22 mg L^?1; SO₄ ^2? 3.90–2,762 mg L^?1; Pb²⁺ 0.023–0.135 mg L^?1; Hg²⁺ 0.0122–0.1231 mg L^?1 Cd²⁺ 0.068–0.416 mg L^?1; Al³⁺ 0.037–1.875 mg L^?1, and Cu²⁺0.006–0.144 mg L^?1. The concentrations of most of the investigated parameters exceeded the recommended limit of the South African Guidelines and World Health Organization tolerance limits for freshwater quality. We conclude that these water bodies are potentially hazardous to public health and this highlights the need for implementation of improved management strategies of these river catchments for continued sustainability.