Residues of organochlorine pesticides in fish from the Egyptian delta lakes

The distribution and residue levels of BHC, Lindane, Endrin, o,p′-DDT, p,p′-DDE, and p,p′-DDD in Mugil and Tilapia species collected from Egyptian Delta lakes were evaluated. Residues of BHC and p,p′-DDT were found in most fish samples obtained from El-Manzala, El-Burullus, Edku, and Maryut lakes. Fish samples from Lake Edku showed the highest residue levels of the studied compounds. Residues of BHC and p,p′-DDT in Mugil and Tilapia species are within the range found in fish from the northwest Atlantic but lower than the levels reported for other fish species the United States. Mugil and Tilapia species could be used as indicator organisms for monitoring the residue levels of organochlorine pesticides and their distribution.     

Co-pyrolysis of sewage sludge and biomass for stabilizing heavy metals and reducing biochar toxicity: A review

The huge amounts of sewage sludge produced by municipal wastewater treatment plants induce major environmental and economical issues, calling for advanced disposal methods. Traditional methods for sewage sludge disposal increase greenhouse gas emissions and pollution. Moreover, biochar created from sewage sludge often cannot be used directly in soil applications due to elevated levels of heavy metals and other toxic compounds, which alter soil biota and earthworms. This has limited the application of sewage sludge-derived biochar as a fertilizer. Here, we review biomass and sewage sludge co-pyrolysis with a focus on the stabilization of heavy metals and toxicity reduction of the sludge-derived biochar. We observed that co-pyrolyzing sewage sludge with biomass materials reduced heavy metal concentrations and decreased the environmental risk of sludge-derived biochar by up to 93%. Biochar produced from sewage sludge and biomass co-pyrolysis could enhance the reproduction stimulation of soil biota by 20‒98%. Heavy metals immobilization and transformation are controlled by the co-feed material mixing ratio, pyrolysis temperature, and pyrolysis atmosphere.

     

Strategies to save energy in the context of the energy crisis: a review

Environmental Chemistry Letters - New technologies, systems, societal organization and policies for energy saving are urgently needed in the context of accelerated climate change, the Ukraine...     

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.     

Phototransformation of oxamyl in aqueous solution

The photolysis of the N methyl carbamate pesticide oxamyl (Z isomer) has been studied in aqueous solution. Continuous irradiation at mainly λ = 254 and λ > 290 nm has been performed to characterise the pesticide photochemical behaviour in water at pH = 6.0. Upon monochromatic irradiation, the phototransformation quantum yield was evaluated to be roughly constant, with a value of 0.54 ± 0.08. Upon polychromatic irradiation, a photochemical efficiency has been estimated to be 0.5 ± 0.1 by using phenol as a reference compound. Two main degradation products were identified: the isomer (E) of oxamyl and the nitrile derivative (N,N-dimethyl-2-nitrilo-acetamide). The photolysis of the oximino derivative, an hydrolysis product of oxamyl, was also studied. Upon irradiation at 254 nm, the quantum yield of phototransformation was found to be 0.28. A unique photoproduct was detected: it corresponds to the (E) isomer of the oximino derivative. For prolonged irradiations, a photostationary state was reached between the oximino and its (E) isomer. From kinetics data, the removal of oxamyl and of the oximino derivative during a UV disinfection step used in drinking water production was calculated to be 45 and 13%, respectively.     

Modelling succession of Eastern Canadian mixedwood forest

The succession of a mixed species stand of the Acadian Forest was simulated by adopting an approach taken by Botkin et al. (1972) (JABOWA) and later modified by Shugart and West (1977) (FORET). The model simulates the dynamic aspects of successional behaviour of the stand by projecting the current stage of vegetation composition (size of each individual of each species present on a 1/12 ha plot) with an element of randomness. The growth of each tree is modeled as a function of its size (represented by its diameter at breast height (dbh), height and leaf area index), the climate, the tree's tolerance to shade and the competition for available resources and space. Stand aboveground biomass (metric ton/ha), leaf area index, number of trees/ha and species composition of the stand were simulated under seven different conditions: (a) normal treatment, (b) increasing biomass maximum 30%, (c) decreasing biomass maximum 30%, (d) increasing degree-days 30%, (e) decreasing degree-days 30%, (f) increasing light extinction coefficient 30% and (g) decreasing light extinction coefficient 30%. Under the first set of conditions (normal treatment), the aboveground biomass reached a maximum value during the first hundred years, decreased during the second, and remained stable for the rest of the 500-year simulation period. The leaf area showed a similar pattern. The total number of trees/ha decreased sharply during the first fifty years and reached a stable value by the end of the first hundred years. Successional patterns and species competitive abilities were interpreted from the accumulated biomass of each species over the simulation period under the different treatments.Species composition of the stand under the normal treatment showed dominance of deciduous species at early stages of succession, with conifer species being increased and becoming dominant at the end of the simulation period. When the climate was raised 30% (warmer) over the average, the deciduous species continued their dominance over the course of the simulation period. Other simulated species dynamics also appeared to follow what is known about their successional behaviour in the field.     

Hydrolysis of organophosphate insecticides in aqueous media

Hydrolysis of crucron [0-(4-bromo-2-chorophenyl)-ethyl-s-n-propyl phosphorothioate], bromophos [0-(4-bromo-2,5-dichlorophenyl)0,0-dimethyl phosphorothioate] and fenitrothion [0,0-dimethyl-0-(4-nitro-m-tolyl phosphorothioate] was investigated in buffered aqueous media at various pH values. Rate constants and half-life studies revealed that these insecticides were relatively stable in acidic medium, and their stability decreased as the pH increased. The mode of decomposition of these compounds in acidic; the neutral medium is dealkylation which results in deakylated compounds and alcohols. In an alkaline medium they undergo hydrolysis resulting in the formation of phenol derivatives and dialkylphosphoric acid.     

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.