Polybrominated diphenyl ethers (PBDEs) in leachates from selected landfill sites in South Africa

The last few decades have seen dramatic growth in the scale of production and the use of polybrominated diphenyl ethers (PBDEs) as flame retardants. Consequently, PBDEs such as BDE -28, -47, -66, -71, -75, -77, -85, -99, -100, -119, -138, -153, -154, and -183 have been detected in various environmental matrices. Generally, in South Africa, once the products containing these chemicals have outlived their usefulness, they are discarded into landfill sites. Consequently, the levels of PBDEs in leachates from landfill sites may give an indication of the general exposure and use of these compounds. The present study was aimed at determining the occurrence and concentrations of most common PBDEs in leachates from selected landfill sites. The extraction capacities of the solvents were also tested. Spiked landfill leachate samples were used for the recovery tests. Separation and determination of the PBDE congeners were carried out with a gas chromatograph equipped with Ni63 electron capture detector. The mean percentage recoveries ranged from 63% to 108% (n=3) for landfill leachate samples with petroleum ether giving the highest percentage extraction. The mean concentrations of PBDEs obtained ranged from ND to 2670pgl(-1), ND to 6638pgl(-1), ND to 7230pgl(-1), 41 to 4009pgl(-1), 90 to 9793pgl(-1) for the Garankuwa, Hatherly, Kwaggarsrand, Soshanguve and Temba landfill sites, respectively. Also BDE -28, -47, -71 and BDE-77 were detected in the leachate samples from all the landfill sites; and all the congeners were detected in two of the oldest landfill sites. The peak concentrations were recorded for BDE-47 at three sites and BDE-71 and BDE-75 at two sites. The highest concentration, 9793+/-1.5pgl(-1), was obtained for the Temba landfill site with the highest BOD value. This may suggest some influence of organics on the level of PBDEs. Considering the leaching characteristics of brominated flame retardants, there is a high possibility that with time these compounds may infiltrate into the groundwater around the sites since most of the sites are not adequately lined.     

Trace metals, anions and polybromodiphenyl ethers in settled indoor dust and their association

Contaminants in settled indoor dust are potentially health hazardous to human. Thus, identification and quantification of toxic chemicals in settled indoor dust is of great concern. In this study, the levels of major anions ( $ \mathrm{C}{{\mathrm{l}}^{-}},\mathrm{N}{{\mathrm{O}}_2}^{-},\mathrm{B}{{\mathrm{r}}^{-}},\mathrm{N}{{\mathrm{O}}_3}^{-},\mathrm{P}{{\mathrm{O}}_4}^{3-}\,\mathrm{and}\,\mathrm{S}{{\mathrm{O}}_4}^{2- } $ ), trace metals (Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd, As and Pb) and polybromodiphenyl ethers (PBDEs) in settled office and home dust were determined and correlations between the contaminants investigated. Depending on the available materials in both microenvironments, the most possible sources were identified. The results showed that the settled office dusts (n?=?6 pooled samples from 85 offices) were more contaminated than home dusts (n?=?8 homes). For anions, $ \mathrm{S}{{\mathrm{O}}_4}^{2- } $ and Cl^– accounted for 87 and 97 % of the total office and home dust contaminants, respectively. For trace metals, Fe, Cu, Zn and Mn, accounted for 98 % of the contaminants in both office and home dust samples. Fe exhibited the highest percentage of 76.7 and 87.3 % in office and home dust samples, respectively. For PBDEs, the mean concentrations detected in office and home dust ranged between 5.8–86.3 and 1.5–20.6 ng?g^?1, respectively. The log-transformed correlation between the total concentrations of trace metals and major anions detected in offices and homes was positive for offices and negative for homes with a statistically significant values (r?=?0.73, p?<?0.01; r?= ?0.22, p?<?0.01, respectively). The daily exposure rates determined for the most hazardous such as As, Cd, Pb and PBDEs congeners, relative to the individual concentrations reported in the literature in settled indoor dust, were found very lower. Therefore, maybe it is possible to expect less potential health risk. Investigation of formation of coordination compounds between trace metals and PBDEs congeners is possible; however, this requires further study.     

The Lower Niger River dredging and indigenous wetland livelihoods in Nigeria: the Anam communities in Ugbolu, Delta State, as a case study

The article explored systemic tendencies for state-led development projects in Nigeria, such as the recently concluded Lower Niger River dredging, to compromise indigenous livelihoods. Development research methods were sensitized with James Ferguson’s antipolitics machine critique and used to elicit participants’ perspectives of the structuring role of the Niger River on their livelihoods, their evaluation of the participatory content of the project and potential project effects on their livelihoods. Participants claimed the Niger River system singularly structures their livelihoods by facilitating recession farming and fishing. In relation to the participatory content and (un)anticipated effects of the dredging project, key informants insisted that it was undemocratically conceived and executed; that the project will reduce the annual Niger River flood, opportunities for recession farming and fishing, impoverish them, induce involuntary migration, and inter-community conflict. Consequently, an inverse relationship was inferred between technicist development programmes or projects conceived and managed by agents of the Nigerian State and the alleged beneficiaries’ versions and experience of structural change. The author also found that the project was exploited by Nigerian development elites to redefine complex regional underdevelopment challenges as infrastructural deficit and relocate discursive blame for underdevelopment from the state and multinational corporations to riverside communities, their cultures and wet ecologies.     

A comparative study of modified and unmodified maize tassels for removal of selected trace metals in contaminated water

Powdered maize tassels were studied and found to exhibit metal sorption properties due to the availability of functional groups. The tassels have a high amount of soluble organic substances that can dissolve in aqueous media, contributing to secondary pollution during a water treatment process. A chelating agent was chemically attached on the maize tassels with a view to increase the sorption capacity, minimize leaching, and enhance the tassels’ stability. Thermogravimetric analysis confirmed that modification improved their thermal stability to withstand temperatures above 600°C as well as reduced the “secondary pollution”. The modified sorbent was employed for the sorption of lead, copper, and cadmium ions in both the model solutions and the real samples. The contact time and pH were optimized after which Langmuir and Freundlich isotherms were applied to the data. The sorption capacities for Cu²⁺, Cd²⁺, and Pb²⁺ improved from 3.4, 0.8, and 1.7?g?kg^?1, respectively, to 6.3, 2.6, and 2.6?g?kg^?1 in the same order. The sorbent was shown to remove up to 95% of the metals in less than 10 min. This study has a potential application for the remediation of polluted waters.     

Determination of urinary lead in school children in Manzini, Swaziland, Southern Africa

Two hundred and fifty-seven urine samples collected from school children living in the Manzini region, Swaziland, were analysed for lead (Pb), using a graphite furnace atomic absorption spectrometer. The mean urine lead concentration for the urban schools ranged from 0.038–0.040 gml^–1, while that for the rural schools ranged from 0.017–0.022 gml^–1. The observed range shown by the urban schools was above the normal (for healthy humans) urine lead concentration of 0.035 gml^–1. However, the mean urine lead concentration for the rural schools was found to be lower than this value. The mean urine lead concentration for the urban schools was significantly higher than that of the rural schools. The differences in the mean urine lead concentrations for boys and girls from both urban and rural schools were found not to be significant, despite the higher values shown by the girls. The difference in lead concentrations between urban and rural schools in Manzini was thought to be due to the traffic density within the urban area.     

Assessment of Lead Exposure in Thohoyandou, South Africa

Lead levels in different environmental media (soil, grass leaves, water, ceramics, pencil, paint, crayons and cosmetics) were determined to assess the major sources of lead exposure in Thohoyandou, South Africa. Soil and plant leaves were used as indicators of Pb pollution from vehicle exhaust emissions. After digestion with concentrated acids (HNO₃, HCl and HClO₄) Pb concentrations were determined in triplicate using a flame atomic absorption spectrometer. The mean Pb concentrations at the kerb of selected busy roads were 205.5 ± 90, 273.0 ± 90 and 312.8 ± 81 μg g⁻¹ and 154.7 ± 67, 182.9 ± 76 and 240.6 ± 66 μg g⁻¹ for soil and plant leaves (dry weight) respectively. These concentrations were substantially higher than the values found on soils 50 m away from the roads (97.4 ± 11 μg g⁻¹). Pb concentrations in plants collected further away from the road (50 m) were substantially lower (71.8 ± 9.0 μg g⁻¹). The observed levels on soil are lower than the UK critical value of 500 μg g⁻¹ for gardens and allotments; and 2000 μg g⁻¹ for parks and open space as well as the Canadian values for agricultural (375 μg g⁻¹), residential (500 μg g⁻¹ and industrial (1000 μg g⁻¹). From these data it was clear that Pb concentrations in soil samples were substantially higher than the levels obtained for plant leaves. The Pb levels in green crayons, blue crayons, pencils (from China & Germany), were 10650 ± 75.2, 8200 ± 52.4, 1160 ± 50.2, 79 ± 10.1 μg g⁻¹ for the inner contents; and 4870 ± 58.1, 5650 ± 55.5, 1950 ± 46.6, 60 ± 12.9 μg g⁻¹ for the outer surface paint respectively. The ceramics showed Pb levels of 630 ± 50.3 μg g⁻¹ (saucer) and 560 ± 32.2 μg g⁻¹ (cup), while the inner contents and outer surface paint showed 480 ± 32.4 and 318 ± 21.2 μg g⁻¹ of Pb respectively. Early morning tap water flush gave a Pb level of 20.6 ± 5.6 μg Pb l⁻¹. This value is higher than the WHO and FDA maximum permissible concentrations of 10 μg l⁻¹ and 15 μg l⁻¹ respectively.     

Distribution of polybrominated diphenyl ethers and dust particle size fractions adherent to skin in indoor dust,Pretoria, South Africa

In order to determine human exposure to the indoor toxicant, selection of dust fraction and understanding dust particle size distribution in settled indoor dust are very important. This study examined the influence of dust particle size on the concentration of polybrominated diphenyl ethers (PBDEs) congeners, assessed the distribution of dust particle size and characterized the main indoor emission sources of PBDEs. Accordingly, the concentrations of PBDE congeners determined in different indoor dust fractions were found to be relatively higher in the order of dust particle size: 45–106 μm?>?(<45 μm)?>?106–150 μm. The finding shows arbitrary selection of dust fractions for exposure determination may result in wrong conclusions. Statistically significant moderate correlation between the concentration of Σ₉PBDEs and organic matter content calculated with respect to the total dust mass was also observed (r?=?0.55, p?=?0.001). On average, of total dust particle size <250 μm, 93.4 % (m/m%) of dust fractions was associated with less than 150 μm. Furthermore, of skin adherent dust fractions considered (<150 μm), 86 % (v/v%) is in the range of particle size 9.25–104.7 μm. Electronic materials treated with PBDEs were found the main emission sources of PBDE congeners in indoor environment. Based on concentrations of PBDEs determined and mass of indoor dust observed, 150 μm metallic sieve is adequate for human exposure risk assessment. However, research in this area is very limited and more research is required to generalize the fact.     

An improved activated carbon method to quantify dichlorodiphenyltrichloroethane (DDT) in surface water

Currently, South Africa is designing a strategy for surface water protection involving organic contaminants such as dichlorodiphenyltrichloroethane (DDT), which is currently used for malaria control in mosquito-infested areas. Here, we demonstrate the successful use of an improved activated carbon technique using dichloromethane instead of chloroform, and slower leaching rate of 15 mL/min to quantify DDT and its metabolites in surface water. The recovery tests for 2,4′DDT, 2,4′DDD, 2,4′DDE, and 4,4′DDT, 4,4′DDD, 4,4′DDE ranged from 75 to 84% and 87 to 96%, respectively (DDE: dichlorodiphenyldichloroethylene, DDD: dichlorodiphenyldichloroethane). The main advantages of this technique over conventional liquid–liquid extractions are reduced amount of organic solvent, little sample preparation, and larger sample throughput. Because activated charcoal is fairly cheap, the technique can be routinely used to quantify and monitor DDT and its metabolites in surface water samples.     

Delonix regia and Casuarina equisetifolia as passive biomonitors and as bioaccumulators of atmospheric trace metals

The suitability of two common and ubiquitously distributed and exotic ornamental plant species in Nigeria-Delonix regia and Casuarina equisetifolia as biomonitors and as effective bioaccumulators of atmospheric trace metals(Cd,Pb,Zn and Cu) has been evaluated.Bark and leaf samples from these plant species were collected in June and July 2006 at five locations in Benin City.Four of the sampling sites were in areas of high traffic density and commercial activities,the fifth site is a remote site,selected to act as a control and also to provide background information for the metals.The plant samples were collected and processed using standard procedures and trace metals were determined using atomic absorption spectrometer.The bark of the plants was able to bioaccumulate the trace metals,especially Pb which originates from anthropogenic contributions in the city.The Pb range of 20.00-70.00 μg/g measured for the bark samples of D.regia,exceeded the normal plant Pb concentration of 0.2-20.0 μg/g and most Pb data available in literature.The bark of the plants was observed to accumulate more metals compared to the leave,while D.regia was found to be slightly better than C.equisetifolia in trace metal uptake efficiency.Spatial variations in the distributions of Pb and Zn were significant(p 0.05),and the continuous use of leaded fuel in Nigeria was identified as the predominant source of Pb in the atmosphere.     

Maize tassel-modified carbon paste electrode for voltammetric determination of Cu(II)

The preparation and application of a practical electrochemical sensor for environmental monitoring and assessment of heavy metal ions in samples is a subject of considerable interest. In this paper, a carbon paste electrode modified with maize tassel for the determination of Cu(II) has been proposed. Scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) were used to study morphology and identify the functional groups on the modified electrode, respectively. First, Cu(II) was adsorbed on the carbon paste electrode surface at open circuit and voltammetric techniques were used to investigate the electrochemical performances of the sensor. The electrochemical sensor showed an excellent electrocatalytic activity towards Cu(II) at pH 5.0 and by increasing the amount of maize tassel biomass, a maximum response at 1:2.5 (maize tassel:carbon paste; w/w) was obtained. The electrocatalytic redox current of Cu(II) showed a linear response in the range (1.23 μM to 0.4 mM) with the correlation coefficient of 0.9980. The limit of detection and current–concentration sensitivity were calculated to be 0.13 (±0.01) μM and 0.012 (±0.001) μA/μM, respectively. The sensor gave good recovery of Cu(II) in the range from 96.0 to 98.0 % when applied to water samples.