6 research outputs found
Respiration of stored intracellular nitrate by eukaryotes and prokaryotes.
<p>A) Example of the appearance of <sup>15</sup>N labeled compounds stored in the sediment during the secondary incubation to which no label was added (example from spring incubations) B) Comparison of the overall fraction of <sup>15</sup>N recovered as either N<sub>2</sub> or NH<sub>4</sub><sup>+</sup> in both the <sup>15</sup>NO<sub>3</sub><sup>−</sup> incubation and the subsequent incubation with no additional <sup>15</sup>NO<sub>3</sub><sup>−</sup> and the partitioning between eukaryotes and prokaryotes C) Eukaryotic denitrification rates E) prokaryotic denitrification rates D) eukaryotic DNRA rates F) prokaryotic DNRA rates. Error bars are SD (n = 3).</p
Exchange of <sup>15</sup>NO<sub>3</sub><sup>−</sup> and <sup>14</sup>NO<sub>3</sub><sup>−</sup> over time in summer incubations.
<p>The dashed line indicates the initial amount of <sup>15</sup>NO<sub>3</sub><sup>−</sup> added to the incubation</p
Seasonal patterns in DNRA rates mediated by the prokaryotic and eukaryotic community.
<p>A) Eukaryotic DNRA rates B) Prokaryotic DNRA rates C) Overall DNRA rates. Total rates were determined from the incubation amended with <sup>15</sup>NO<sub>3</sub><sup>−</sup>. Prokaryotic rates were determined after addition of the eukaryote inhibitor cycloheximide. Eukaryotic rates were calculated by subtracting prokaryotic rates from total rates. Error bars are SD (n = 3)</p
Rates of nitrogen cycling processes determined over 3 seasons.
<p>Anaerobic dissimilatory nitrate reduction to ammonium (DNRA) and denitrification (Denit.) rates from the incubation amended with <sup>15</sup>NO<sub>3</sub><sup>−</sup>. Rates were determined from linear production slopes after oxygen had been consumed. Error bars are SD (n = 3)</p
Comparison of incubation methods.
<p>Incubations were carried out using either membrane inlet mass spectrometry (MIMS) which allowed for continuous online measurements or by discrete porewater sampling into exetainers and subsequent measurement on a GC-IRMS. The example shown is taken from a replicate during the spring incubations directly after the addition of <sup>15</sup>NO<sub>3</sub><sup>−</sup>.</p
Average percentage of <sup>15</sup>N recovered in various pools.
<p>Denitrification denotes <sup>15</sup>N that was present as <sup>29+30</sup>N<sub>2</sub>, DNRA denotes <sup>15</sup>N that was present as <sup>15</sup>NH<sub>4</sub><sup>+</sup> and intracellular storage represents <sup>15</sup>N which was present as either <sup>29+30</sup>N<sub>2</sub> or <sup>15</sup>NH<sub>4</sub> at the termination of the secondary incubation to which no additional <sup>15</sup>NO<sub>3</sub> was added. The ‘missing label’ fraction refers to the discrepancy between added <sup>15</sup>NO<sub>3</sub><sup>−</sup>, measured <sup>15</sup>NO<sub>3</sub><sup>−</sup> and <sup>15</sup>N<sub>2</sub> production (shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0104517#pone-0104517-g004" target="_blank">Fig. 4</a>). Error bars are overall SD (n = 3)</p