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Dyntel Corp., Waterways Experiment Station, 3909 Halls Ferry Road, Vicksburg, MS 39180-6199;
Center for Environ. Biotechnol., Univ. of Tennessee, 10515 Research Dr., Suite 300, Knoxville, TN 37932-2575;
Environ. Sciences Div., Oak Ridge National Lab., Oak Ridge, TN 37831.
* Corresponding author (dringelbe{at}aol.com).
ABSTRACT
The consequences for belowground microbiota under conditions of rising atmospheric CO2 are largely unknown. In this research we examined the microbiota associated with white oak (Quercus alba L.). It was our hypothesis that an increase in CO2 level would induce a change in the rhizosphere-associated microbial abundance and community composition. To provide an in situ estimation of microbial abundance and community composition, ester-linked polar lipid fatty acid (PLFA) technology was utilized. This technology, based on the quantitative measurement of membrane lipid fatty acids, has been utilized in the accurate identification and description of bacterial isolates and communities. Initial experiments demonstrated that a clear distinction in lipid patterns and microbial biomass existed between sterile roots and those of roots containing an associated viable microbiota. Statistical approaches were then used to determine what differences existed between individual PLFA and PLFA patterns obtained from white oak fine roots and bulk soils. An analysis of variance (ANOVA) showed significant differences to exist in the relative percentages of individual prokaryotic PLFA collected under ambient vs. elevated CO2 and between those associated with fine roots and bulk soils. Multivariate statistics showed distinct differences in the patterns of prokaryotic PLFA detected in the rhizosphere vs. the surrounding bulk soil, but did not identify differences related to elevated CO2 exposures. An artificial neural network recognized PLFA patterns unique to three different CO2 exposures:
35,
50, and
65 Pa. Results of the three statistical tests were viewed as supportive of the hypothesis describing significant differences in individual PLFA and patterns of PLFA as a result of elevated CO2 exposure.
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