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Biomedical subjects

James J Germida

Publications and source records attributed to James J Germida.

7 recordsLinked to original sources

Plant-assisted degradation of phenanthrene as assessed by solid-phase microextraction (SPME).

The soil bacterium Sphingomonas yanoikuyae was isolated from a petroleum-contaminated soil and grown on mineral salts agar overlaid with the polycyclic aromatic hydrocarbon phenanthrene. The effect of white mustard, Sinapis alba, on phenanthrene degradation by S. yanoikuyae in artificially contaminated Redi-earth-sand was examined. Solid-phase-microextraction (SPME) gas chromatography-flame ionization detection (GC-FID) was used to quantify the concentration of phenanthrene in the gas phase of Magenta jars containing S. alba and S. yanoikuyae, each alone and with no additions. Gas chromatography-mass spectrometry (GC-MS) of Soxhlet extracts was used to determine the concentration of phenanthrene remaining in Redi-earth-sand. The gas phase concentration of phenanthrene in nonsterile Redi-earth-sand decreased by 99.7% in treatments with S. alba plus S. yanoikuyae, by 98.6% with S. alba, by 96.7% with S. yanoikuyae, and by 95.8% with no additions. Under gnotobiotic conditions, the gas phase concentration of phenanthrene in Redi-earth-sand decreased by 94% in treatments with S. alba plus S. yanoikuyae, by 77% with S. yanoikuyae, by 26% with S. alba, and 0% with no additions. The concentration of phenanthrene in Redi-earth-sand under gnotobiotic conditions decreased in treatments with S. alba plus S. yanoikuyae by 88%, by 67% with S. yanoikuyae, by 13% with S. alba, and 0% with no additions as measured in Soxhlet extracts. These results suggest that SPME-GC can be used to rapidly assess the potential of plants and microorganisms to reduce the level of unaged polyaromatic hydrocarbons such as phenanthrene in soil. This method provided results that were consistent with the more costly Soxhlet extraction method and was less time consuming.

Biodegradation, Environmental↗

Ability of cold-tolerant plants to grow in hydrocarbon-contaminated soil.

Phytoremediation of hydrocarbons in soil involves plants and their associated microorganisms. Differences in environmental conditions and restrictions on species importation mean that each country may need to identify indigenous plants to use for phytoremedation. Screening plants for hydrocarbon tolerance before screening for degradation ability may prove more economical than screening directly for degradation. Thirty-nine cold-tolerant plants native, or exotic and naturalized, in western Canada were assessed for their ability to survive in crude oil-contaminated soil. Four naturalized grasses (i.e., Agropyron pectiniforme, Bromus inermis, Phleum pratense, and Poa pratensis), three naturalized legumes (i.e., Medicago sativa, Melilotus officinalis, and Trifolium repens), two native forbs (i.e., Artemisia frigida and Potentilla pensylvanica), one native grass (i.e., Bromus ciliatus) and two native legumes (i.e., Glycyrrhiza lepidota and Psoralea esculenta) exhibited phytoremediation potential, based on survival. We determined the effect of increasing crude oil concentrations on total and root biomass, and relative growth rate of those species with the highest survival. The addition of 0.5%, 1%, and 5% (crude oil wt/fresh soil wt) crude oil to soil significantly decreased both the total biomass by at least 22% of the control and the relative growth rate of all species except P. esculenta. Root biomass significantly decreased by at least 22% with crude oil addition in all species except P. esculenta and A. frigida. Total biomass production in contaminated soil had a significant negative correlation with the relative growth rate in uncontaminated soil.

Acclimatization↗

Changes in microbial community composition and function during a polyaromatic hydrocarbon phytoremediation field trial.

The purpose of this study was to investigate the mechanism by which phytoremediation systems promote hydrocarbon degradation in soil. The composition and degradation capacity of the bulk soil microbial community during the phytoremediation of soil contaminated with aged hydrocarbons was assessed. In the bulk soil, the level of catabolic genes involved in hydrocarbon degradation (ndoB, alkB, and xylE) as well as the mineralization of hexadecane and phenanthrene was higher in planted treatment cells than in treatment cells with no plants. There was no detectable shift in the 16S ribosomal DNA (rDNA) composition of the bulk soil community between treatments, but there were plant-specific and -selective effects on specific catabolic gene prevalence. Tall Fescue (Festuca arundinacea) increased the prevalence of ndoB, alkB, and xylE as well as naphthalene mineralization in rhizosphere soil compared to that in bulk soil. In contrast, Rose Clover (Trifolium hirtum) decreased catabolic gene prevalence and naphthalene mineralization in rhizosphere soil. The results demonstrated that phytoremediation systems increase the catabolic potential of rhizosphere soil by altering the functional composition of the microbial community. This change in composition was not detectable by 16S rDNA but was linked to specific functional genotypes with relevance to petroleum hydrocarbon degradation.

Bacteria↗

Seasonal changes in the rhizosphere microbial communities associated with field-grown genetically modified canola (Brassica napus).

The introduction of transgenic plants into agricultural ecosystems has raised the question of the ecological impact of these plants on nontarget organisms, such as soil bacteria. Although differences in both the genetic structure and the metabolic function of the microbial communities associated with some transgenic plant lines have been established, it remains to be seen whether these differences have an ecological impact on the soil microbial communities. We conducted a 2-year, multiple-site field study in which rhizosphere samples associated with a transgenic canola variety and a conventional canola variety were sampled at six times throughout the growing season. The objectives of this study were to identify differences between the rhizosphere microbial community associated with the transgenic plants and the rhizosphere microbial community associated with the conventional canola plants and to determine whether the differences were permanent or depended on the presence of the plant. Community-level physiological profiles, fatty acid methyl ester profiles, and terminal amplified ribosomal DNA restriction analysis profiles of rhizosphere microbial communities were compared to the profiles of the microbial community associated with an unplanted, fallow field plot. Principal-component analysis showed that there was variation in the microbial community associated with both canola variety and growth season. Importantly, while differences between the microbial communities associated with the transgenic plant variety were observed at several times throughout the growing season, all analyses indicated that when the microbial communities were assessed after winter, there were no differences between microbial communities from field plots that contained harvested transgenic canola plants and microbial communities from field plots that did not contain plants during the field season. Hence, the changes in the microbial community structure associated with genetically modified plants were temporary and did not persist into the next field season.

Bacteria↗

Growth of Indigenous Rhizobium leguminosarum and Rhizobium meliloti in Soils Amended with Organic Nutrients.

The ability of indigenous Rhizobium leguminosarum and Rhizobium meliloti to use organic nutrients as growth substrates in soil was assessed by indirect bacteriophage analysis. A total of 17 organic compounds, including 9 carbohydrates, 3 organic acids, and 5 amino acids, were tested (1,000 mug g) in three soils with different cropping histories. Four additional soils were screened with a glucose amendment. Nutrient amendments stimulated growth of indigenous rhizobia, allowing subsequent replication of indigenous bacteriophages. Phage populations were enumerated by plating soil extracts on 19 R. leguminosarum and 9 R. meliloti indicator strains, including root nodule isolates from the soils assayed. On the basis of indirect phage analysis, all soils contained native rhizobia similar to one or more of the indicator strains, although not all indicator strains were detected in soil. All organic compounds stimulated growth of indigenous rhizobia, but the growth response varied for each rhizobial strain depending on the nutrient, the nutrient concentration, and the soil. Indigenous rhizobia readily utilized most organic compounds except phenylalanine, glycine, and aspartic acid. The ability of indigenous rhizobia to utilize a wide range of organic compounds as growth substrates in situ indicates their ability to successfully compete with other soil bacteria for nutrients in these soils.

Journal Article↗

Are methylmercury concentrations in the wetlands of Kejimkujik National Park, Nova Scotia, Canada, dependent on geology?

In the relatively pristine ecosystem in Kejimkujik Park, Nova Scotia, methylmercury (MeHg) concentrations in loons, Gavia immer, are among the highest recorded anywhere in the world. This study investigated the influence of bedrock lithology on MeHg concentrations in wetlands. Twenty-five different wetland field sites were sampled over four different bedrock lithologies; Kejimkujik monzogranite, black sulfidic slate, gray slate, and greywacke. Soil samples were analyzed for ethylmercury (EtHg), MeHg, total Hg, acid-volatile sulfides (AVS), organic matter, and water content as well as the biological parameters, mercury methyltransferase (HgMT) activity, sulfate reduction rates, fatty acid methyl ester (FAME) composition, and acidity. Methylmercury concentrations in the wetlands were highly dependent (P < 0.08) on lithology with no significant difference between bogs, fens, and swamps. Methylmercury concentrations in wetland soils developed on Kejimkujik monzogranite averaged 900 ng kg(-1) compared with only 300 ng kg(-1) in wetland soils developed on black sulfidic slate. Fatty acid methyl ester composition was also lithologically dependent (P < 0.001) with biomarkers for Desulfobulbus spp. discriminating between sites containing high and low MeHg concentrations. Levels of MeHg in wetlands were predicted mainly (41% of the sum of squares) by HgMT activity that differed (P < 0.009) between wetlands, with activity in bogs almost three times that present in swamps. Wetland MeHg concentrations are highly dependent on the lithology on which they have developed for largely biological reasons.

Animals↗

Impact of genetically modified crops on soil- and plant-associated microbial communities.

Transgenic or genetically modified plants possess novel genes that impart beneficial characteristics such as herbicide resistance. One of the least understood areas in the environmental risk assessment of genetically modified crops is their impact on soil- and plant-associated microbial communities. The potential for interaction between transgenic plants and plant residues and the soil microbial community is not well understood. The recognition that these interactions could change microbial biodiversity and affect ecosystem functioning has initiated a limited number of studies in the area. At this time, studies have shown the possibility that transgenes can be transferred to native soil microorganisms through horizontal gene transfer, although there is not evidence of this occurring in the soil. Furthermore, novel proteins have been shown to be released from transgenic plants into the soil ecosystem, and their presence can influence the biodiversity of the microbial community by selectively stimulating the growth of organisms that can use them. Microbial diversity can be altered when associated with transgenic plants; however, these effects are both variable and transient. Soil- and plant-associated microbial communities are influenced not only by plant species and transgene insertion but also by environmental factors such as field site and sampling date. Minor alterations in the diversity of the microbial community could affect soil health and ecosystem functioning, and therefore, the impact that plant variety may have on the dynamics of the rhizosphere microbial populations and in turn plant growth and health and ecosystem sustainability, requires further study.

Bacteria↗