Nitrogen Ferttilizers and Their Effects on Microbial Biodivresity.

Denaturing gradient gel electrophoresis (DGGE) is a useful technology in assessing the microbial diversity in a soil environment.  In this study the bacterial diversity was investigated in an agricultural environment.  Objectives investigated were if nitrogen or mode of nitrogen affects the soil biodiversity, if manure or amount of manure affects biodiversity, or if the combination of the two affects biodiversity. The two chemical fertilizers used were ammonium nitrate and polymer base slow release fertilizer at two levels (100 and 400 pounds per acre foot slide).  The chemical fertilizers were applied to a heavy manure history of over twenty years of application plot, a little manure history less than five years of application of manure plot, and a no manure plot.  Samples were collected before time of application and at three time points following (11 days, 28 days, and 28 days respectively).  Following DNA extraction the V2-V3 region of the 16s rRNA  (16srDNA) were PCR amplified with the eubacterium specific primers 341 fgc-GC clamp and the 534 r.  DGGE banding patterns were compared between treatment levels and plot applied.  There were difference in bacterial community profiles when comparing chemical fertilizer treatment and organic amendment differences. 

Denaturing gradient gel electrophoresis (DGGE) is a useful technology in assessing the microbial diversity in a soil environment.  In this study the bacterial diversity was investigated in an agricultural environment.  Objectives investigated were if nitrogen or mode of nitrogen affects the soil biodiversity, if manure or amount of manure affects biodiversity, or if the combination of the two affects biodiversity. The two chemical fertilizers used were ammonium nitrate and polymer base slow release fertilizer at two levels (100 and 400 pounds per acre foot slide).  The chemical fertilizers were applied to a heavy manure history of over twenty years of application plot, a little manure history less than five years of application of manure plot, and a no manure plot.  Samples were collected before time of application and at three time points following (11 days, 28 days, and 28 days respectively).  Following DNA extraction the V2-V3 region of the 16s rRNA  (16srDNA) were PCR amplified with the eubacterium specific primers 341 fgc-GC clamp and the 534 r.  DGGE banding patterns were compared between treatment levels and plot applied.  There were difference in bacterial community profiles when comparing chemical fertilizer treatment and organic amendment differences.