Results/Conclusions
The ratio of archaeal to bacterial amoA genes was lowest in forested upland soils (approximately 1) and highest in agricultural lowland soils (3 – 40). Both AOA and AOB amoA abundance was higher in high versus low nutrient upland soil (1 x 107 vs. 1 x 106 amoA gene copies g-1 dry soil for both bacteria and archaea), but only AOA amoA abundance was higher in high versus low nutrient lowland soil (4 x 107 vs. 2 x 106 amoA gene copies g-1 dry soil). Nitrification potential ranged from 0.3 to 1.5 μmol nitrate plus nitrite g-1 dry soil h-1, and was higher in all high nitrogen soils relative to low nitrogen soils. Terminal restriction fragment length polymorphism (T-RFLP) fingerprints of amoA showed different communities of both AOA and AOB in the different soil types. In addition, T-RLFP profiles showed that high and low nitrogen lowland soils harbored distinct bacterial amoA communities, but similar archaeal amoA communities. Using data from both field distribution and lab manipulation of soil conditions, we are investigating further whether and how environmental differences affect the relative abundance and activity of AOA and AOB in these soils. This study provides a template for learning more about the niche preferences of ammonia-oxidizing archaea and bacteria, and about the environmental conditions that influence nitrification activity by both microbial groups.