/AnMtgsAbsts2009.56629 Low-Input Production of Switchgrass Using Plant Growth Promoting Rhizobacteria.

Tuesday, November 3, 2009
Convention Center, Exhibit Hall BC, Second Floor

Keomany Ker1, James W. Fyles2, Brian T. Driscoll2, Philippe Seguin3 and Donald Smith3, (1)Department of Natural Resource Sciences, McGill Univ., Macdonald Campus, Ste-Anne de Bellevue, QC, Canada
(2)Department of Natural Resource Sciences, McGill Univ., Macdonald Campus, Ste-Anne-de-Bellevue, QC, Canada
(3)Department of Plant Science, McGill Univ., Macdonald Campus, Ste-Anne-de-Bellevue, QC, Canada
Poster Presentation
  • 2009ASA.pdf (22.8 MB)
  • Abstract:
    Switchgrass (Panicum virgatum) is being examined as the prime candidate for biofuel feedstock production in North America because it can be grown on marginal lands with minimal agricultural inputs and thus does not displace food production. Variety trials were conducted in Ste-Anne-de-Bellevue, Quebec, Canada (45°28’N 73°45’W) on 11 different upland switchgrass varieties including Cave-In-Rock, Carthage, and several cultivars from the U. of Nebraska and Oklahoma. The trial was initiated in 1996, and managed until 2000 after which no fertilizer was applied. The switchgrass has continued to produce high biomass yields without N fertilization, which suggests an alternative N source perhaps through biological nitrogen fixation. We hypothesized that a) indigenous populations of rhizosphere N2-fixing bacteria have provided switchgrass with the N necessary for substantial biomass growth, and b) productivity differences amongst varieties are due to variation and abundance of N2-fixing bacterial populations.

    In 2008, rhizosphere soil, root and rhizome samples were collected from this field site. Endophytic (> 300) and epiphytic (> 500) putative N2-fixing bacteria were isolated on N-free solid media. Bacterial screening bioassays were performed in a growth chamber on inoculated and uninoculated (control) switchgrass plants (P.virgatum cv. Cave-In-Rock) fertilized with N-free Hoagland’s solution. Isolates that show plant growth promotion will be selected for identification using phylogenetic anaylsis of the 16S rRNA. Amplification of nifH gene will be used as a marker for N2-fixation capability. Those isolates that show production of the greatest amount of plant biomass will be chosen for further field experimentation. The results of this project will advance our management of purpose grown grasses and existing grasslands. The development of biofuel crop systems that require low N input will improve both the economics and energetics of biofuel production, enhancing the use of biofuels as a sustainable energy source and support rural renewal.