Phospholipid Fatty Acid Profiles of Bacteria and Fungi in Peat Exposed to Experimentally Increased N Deposition, 2015

Development of the oil sands has led to increasing atmospheric N deposition, with values as high as 17 kg N ha -1 yr -1 ; regional background levels <2 kg N ha -1 yr -1 . Bogs, being ombrotrophic, may be especially susceptible to increasing N deposition. To examine responses to N deposition, over...

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Bibliographic Details
Main Authors: R Kelman Wieder, Dale H Vitt, Melanie A Vile, Jeremy A Graham, Jeremy A Hartsock, Hope Fillingim, Melissa House, James C Quinn, Kimberli D Scott, Meaghan Petix, Kelly J McMillen
Format: Dataset
Language:unknown
Published: Environmental Data Initiative 2019
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Online Access:https://pasta.lternet.edu/package/metadata/eml/edi/365/1
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Summary:Development of the oil sands has led to increasing atmospheric N deposition, with values as high as 17 kg N ha -1 yr -1 ; regional background levels <2 kg N ha -1 yr -1 . Bogs, being ombrotrophic, may be especially susceptible to increasing N deposition. To examine responses to N deposition, over five years, we experimentally applied N (as NH 4 NO 3 ) to a bog near Mariana Lakes, Alberta, at rates of 0, 5, 10, 15, 20, and 25 kg N ha -1 yr -1 , plus controls (no water or N addition). In July of 2015 we measured PLFA markers in two depths in each plot. For the most part, microbial group abundances were not affected by increasing N input (Fig. 16). However, actinomycete abundance decreased with increasing N deposition at rates that were similar in 0-5 and 5-10 cm peat. Gram-negative bacteria increased slightly with increasing N input and were more abundant in 0-5 cm than in 5-10 cm peat; correspondingly the Gram-positive to Gram-negative bacterial ratio decreased with increasing N input and was lower in 0-5 cm than in 5-10 cm peat. Total microbial abundance and total bacterial abundance were significantly higher in 0-5 cm peat than in 5-10 cm peat. It may be that more sensitive/targeted techniques, such as high-throughput pyrosequencing, 16s RNA clone library analysis and rRNA-targeted fluorescence in situ hybridization (FISH) or whole genome shotgun sequencing may be required to reveal bog microbial community responses to N loading.