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1.
Can J Microbiol ; 57(10): 775-84, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21936679

RESUMO

The increasing use of treated wastewater for irrigation heightens the importance of accurate monitoring of water quality. Chromogenic media, because they are easy to use and provide rapid results, are often used for detection of Escherichia coli in environmental samples, but unique levels of organic and inorganic compounds alter the chemistry of treated wastewater, potentially hindering the accurate performance of chromogenic media. We used MI agar and molecular confirmatory methods to assess false-positive identification of E. coli in treated wastewater samples collected from municipal utilities, an irrigation holding pond, irrigated soils, and in samples collected from storm flows destined for groundwater recharge. False-positive rates in storm flows (4.0%) agreed closely with USEPA technical literature but were higher in samples from the pond, soils, and treatment facilities (33.3%, 38.0%, and 48.8%, respectively). Sequencing of false-positive isolates confirmed that most were, like E. coli, of the family Enterobacteriaceae, and many of the false-positive isolates were reported to produce the ß-D-glucuronidase enzyme targeted by MI agar. False-positive identification rates were inversely related to air temperature, suggesting that seasonal variations in water quality influence E. coli identification. Knowledge of factors contributing to failure of chromogenic media will lead to manufacturer enhancements in media quality and performance and will ultimately increase the accuracy of future water quality monitoring programs.


Assuntos
Técnicas Bacteriológicas/métodos , Meios de Cultura/química , Erros de Diagnóstico , Escherichia coli/isolamento & purificação , Água Subterrânea/microbiologia , Esgotos/microbiologia , Compostos Cromogênicos/metabolismo , Técnicas de Diagnóstico Molecular/métodos , Estações do Ano , Temperatura , Qualidade da Água/normas
2.
Biodegradation ; 18(2): 133-44, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16897581

RESUMO

Sandy clay loam soil was contaminated with 5000 mg kg(-1) diesel, and amended with nitrogen (15.98 atom% (15)N) at 0, 250, 500, and 1000 mg kg(-1) to determine gross rates of nitrogen transformations during diesel biodegradation at varying soil water potentials. The observed water potential values were -0.20, -0.47, -0.85, and -1.50 MPa in the 0, 250, 500, and 1000 mg kg(-1) nitrogen treatments respectively. Highest microbial respiration occurred in the lowest nitrogen treatment suggesting an inhibitory osmotic effect from higher rates of nitrogen application. Microbial respiration rates of 185, 169, 131, and 116 mg O(2) kg(-1) soil day(-1) were observed in the 250, 500, control and 1000 mg kg(-1) nitrogen treatments, respectively. Gross nitrification was inversely related to water potential with rates of 0.2, 0.04, and 0.004 mg N kg(-1) soil day(-1) in the 250, 500, and 1000 mg kg(-1) nitrogen treatments, respectively. Reduction in water potential did not inhibit gross nitrogen immobilization or mineralization, with respective immobilization rates of 2.2, 1.8, and 1.8 mg N kg(-1) soil day(-1), and mineralization rates of 0.5, 0.3, and 0.3 mg N kg(-1) soil day(-1) in the 1000, 500, and 250 mg kg(-1) nitrogen treatments, respectively. Based on nitrogen transformation rates, the duration of fertilizer contribution to the inorganic nitrogen pool was estimated at 0.9, 1.9, and 3.2 years in the 250, 500, and 1000 mg kg(-1) nitrogen treatments, respectively. The estimation was conservative as ammonium fixation, gross nitrogen immobilization, and nitrification were considered losses of fertilizer with only gross mineralization of organic nitrogen contributing to the most active portion of the nitrogen pool.


Assuntos
Biodegradação Ambiental , Poluentes Ambientais/análise , Recuperação e Remediação Ambiental , Fertilizantes/análise , Gasolina , Nitrogênio/química , Solo/análise , Algoritmos , Amônia/química , Nitratos/química , Radioisótopos de Nitrogênio , Técnica de Diluição de Radioisótopos , Solubilidade
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