Food contamination as a pathway for lead exposure in children during the 2010–2013 lead poisoning epidemic in Zamfara, Nigeria

In 2010, an estimated 400 to 500 children died of acute lead poisoning associated with artisanal gold mining in Zamfara, Nigeria. Processing of gold ores containing up to 10% lead within residential compounds put residents, especially children, at the highest risk. Principal routes of exposure were incidental ingestion and inhalation of contaminated soil and dusts. Several Nigerian and international health organizations collaborated to reduce lead exposures through environmental remediation and medical treatment. The contribution of contaminated food to total lead exposure was assessed during the environmental health response. Objectives of this investigation were to assess the influence of cultural/dietary habits on lead exposure pathways and estimate the contribution of contaminated food to children's blood lead levels(BLLs). A survey of village dietary practices and staple food lead content was conducted to determine dietary composition, caloric intakes, and lead intake. Potential blood lead increments were estimated using bio-kinetic modeling techniques. Most dietary lead exposure was associated with contamination of staple cereal grains and legumes during post-harvest processing and preparation in contaminated homes. Average post-harvest and processed cereal grain lead levels were 0.32 mg/kg and 0.85 mg/kg dry weight, respectively. Age-specific food lead intake ranged from 7 to 78 μg/day. Lead ingestion and absorption were likely aggravated by the dusty environment, fasting between meals, and nutritional deficiencies. Contamination of staple cereal grains by highly bioavailable pulverized ores could account for as much as 11%–34% of children's BLLs during the epidemic, and were a continuing source after residential soil remediation until stored grain inventories were exhausted.     

Monitoring Ambient Sulfur Dioxide Levels at some Residential Environments in the Greater Cairo Urban Region – Egypt

The impact of the increased sulfur dioxide emissions within the Greater Cairo Urban Region over the part 50 yr has been overwhelming. While previous air-pollution surveys measuring SO2 levels in the region converged upon the study of emissions from specific industrial activities, no correlation between the measured concentrations and the induced health-related impacts in living environments was provided. As well, no inventory of emissions from other sources within some residential areas were accounted for or evaluated. During the study period of January to April 2000, the ambient sulfur dioxide levels in four residential locations within the capital region were investigated. The results indicated that the measured cumulative ambient SO2 concentrations were in excess of the national and the international monthly mean exposure limits, irrespective of the type of local activity. As well, measurements within three of the selected environments surpassed the 0.5 ppm SO2 odor-threshold. The data also showed a significant dependency of the measured content upon the physical layout and topography of the studied environment as well as with respect to the prevailing seasonal weather conditions.     

Volatile organic compounds in some urban locations in United States

Volatile organic compounds (VOCs) have been determined to be human risk factors in urban environments, as well as primary contributors to the formation of photochemical oxidants. Ambient air quality measurements of 54 VOCs including hydrocarbons, halogenated hydrocarbons and carbonyls were conducted in or near 13 urban locations in the United States during September 1996 to August 1997. Air samples were collected and analyzed in accordance with US Environmental Protection Agency-approved methods. The target compounds most commonly found were benzene, toluene, xylene and ethylbenzene. These aromatic compounds were highly correlated and proportionally related in a manner suggesting that the primary contributors were mobile sources in all the urban locations studied. Concentrations of total hydrocarbons ranged between 1.39 and 11.93 parts per billion, by volume (ppbv). Ambient air levels of halogenated hydrocarbons appeared to exhibit unique spatial variations, and no single factor seemed to explain trends for this group of compounds. The highest halogenated hydrocarbon concentrations ranged from 0.24 ppbv for methylene chloride to 1.22 ppbv for chloromethane. At participating urban locations for the year of data considered, levels of carbonyls were higher than the level of the other organic compound groups, suggesting that emissions from motor vehicles and photochemical reactions strongly influence ambient air concentrations of carbonyls. Of the most prevalent carbonyls, formaldehyde and acetaldehyde were the dominant compounds, ranging from 1.5-7.4 ppbv for formaldehyde, to 0.8-2.7 ppbv for acetaldehyde.     

Fuzzy goal programming for biodiesel production

ABSTRACT

The energy consumed around the world and especially in Morocco is dominated by oil products. The latter; whether in the global or the national context; are mainly due to diesel, whose climate impacts are well established, suggesting the search for a greener alternative. Despite its virtues, biodiesel is struggling to impose itself for purely economic reasons. Thus, in order to offer a sustainable solution, while keeping in mind the unpredictable fluctuations (price, demand …). This work proposes a generalization of fuzzy goal programming into fully fuzzy goal programming and a relative application, where the aim is to have a final product at a competitive price.     

Photodegradation of atrazine and ametryn with visible light using water soluble porphyrins as sensitizers

The photodegradation of the herbicides atrazine and ametryn with visible light in aerated neutral aqueous solutions and 5, 10, 15, 20-tetrakis (2,6-dichloro-3-sulfophenyl) porphyrin or 5, 10, 15, 20-tetrakis (4-sulfophenyl) porphyrin as sensitizers are reported for the first time. Our findings show that the degradation percentage reached 30% for atrazine and 63% for ametryn. The final photoproducts were characterized as dealkylated s-triazines. Photolysis of the pesticides in the presence of a singlet oxygen quencher showed only a minor contribution of this type of mechanism, while a bimolecular quenching reaction between the triplet state of the sensitizer and the pesticides is excluded by flash photolysis studies. It is proposed that the mechanism may involve the formation of a superoxide radical anion from the triplet state of the sensitizer and molecular oxygen, followed by a radical decomposition pathway. Selected article from 1st International Meeting on Photochemistry, Photocatalysis and Environmental Applications, Agadir, 2006, organised by Prof. Dr. Ait Ichou, University Ibn Zohr, Agadir, Morocco     

Highly efficient photodegradation of the pesticide metolcarb induced by Fe complexes

Here we show the efficient photoinduced degradation of the pesticide metolcarb, in less than 400 min, using iron(III) aquacomplexes and 365 nm light. The degradation is mainly due to the formation of hydroxyl radical. It was complete when molecular oxygen was present. The analytical study gives evidence for the primary formation of several byproducts formed from 1) the scission of the O–C bond, 2) the hydroxylation of the aromatic moiety and 3) the attack of the two methyl groups. Under prolonged irradiation and in aerated solutions, efficient mineralization was evidenced by the study of total organic carbon evolution as a function of irradiation time.     

Remediation of heavy metal contaminated soils via integrated electrochemical processes

The thrust of this study is to develop an in-situ method/technique capable of modifying the contaminated soil environment and maximizing contaminant extraction. Contaminated soils were compacted in electrokinetic cells to densities similar to natural field conditions. Conditioning fluids were used during the application of a direct current to solubilize the precipitated forms of heavy metals. Mobilization of contaminants as a function of time was quantified by analysing metal ion concentrations in the extracted effluents at both the anode and cathode and in the compacted specimens. For each conditioning fluid used, the removal efficiencies were evaluated based on both effluent and soil concentrations.