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Respiration and bacterial carbon dynamics in the Amundsen Gulf, western Canadian Arctic

Identifieur interne : 001E02 ( Istex/Corpus ); précédent : 001E01; suivant : 001E03

Respiration and bacterial carbon dynamics in the Amundsen Gulf, western Canadian Arctic

Auteurs : Dan Nguyen ; Roxane Maranger ; Jean-Éric Tremblay ; Michel Gosselin

Source :

RBID : ISTEX:8A918C6816F4AD3767E8A6151364162795FD8559

Abstract

Respiration rates are fundamental to understanding ecosystem C flux; however, respiration remains poorly characterized in polar oceans. The Circumpolar Flaw Lead (CFL) study provided a unique opportunity to sample the Amundsen Gulf, from November 2007 to July 2008 and follow microbial C dynamics. This study shows that bacterial production (BP) was highly variable, ranging from 0.01 to 2.14 μg C L−1 d−1 (CV = 192%), whereas the range in community respiration (CR) was more conservative from 3.8 to 44.2 μg C L−1 d−1 (CV = 55%), with measurable rates throughout the year. The spring‐summer peak in BP preceded the peak in CR suggesting differential predominant control. From May until July, BP was more related to chlorophyll a concentration (r = 0.68) whereas CR was not. Given the observed high variability, BP was the main driver of bacterial growth efficiency (BGE) (r2 = 0.86). The overall average BGE was low at 4.6%, ranging from 0.20 in winter to a peak of 18.6% during the spring bloom. This study confirms that respiration is an important fate for C in the Amundsen Gulf, and our rate‐based estimates of ecosystem scale CR suggests that considerably more C is respired than could be accounted for by gross primary production (GPP). One of the most plausible explanations for this observed discrepancy is that regenerated primary production is currently underestimated.

Url:
DOI: 10.1029/2011JC007343

Links to Exploration step

ISTEX:8A918C6816F4AD3767E8A6151364162795FD8559

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<p xml:id="jgrc12234-para-0001">Auxiliary material for this article contains a figure, a table, and a short discussion describing the potential effect of temperature correction on respiration rates.</p>
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<p xml:id="jgrc12234-para-0004" label="1">Respiration rates are fundamental to understanding ecosystem C flux; however, respiration remains poorly characterized in polar oceans. The Circumpolar Flaw Lead (CFL) study provided a unique opportunity to sample the Amundsen Gulf, from November 2007 to July 2008 and follow microbial C dynamics. This study shows that bacterial production (BP) was highly variable, ranging from 0.01 to 2.14
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<abstract>Respiration rates are fundamental to understanding ecosystem C flux; however, respiration remains poorly characterized in polar oceans. The Circumpolar Flaw Lead (CFL) study provided a unique opportunity to sample the Amundsen Gulf, from November 2007 to July 2008 and follow microbial C dynamics. This study shows that bacterial production (BP) was highly variable, ranging from 0.01 to 2.14 μg C L−1 d−1 (CV = 192%), whereas the range in community respiration (CR) was more conservative from 3.8 to 44.2 μg C L−1 d−1 (CV = 55%), with measurable rates throughout the year. The spring‐summer peak in BP preceded the peak in CR suggesting differential predominant control. From May until July, BP was more related to chlorophyll a concentration (r = 0.68) whereas CR was not. Given the observed high variability, BP was the main driver of bacterial growth efficiency (BGE) (r2 = 0.86). The overall average BGE was low at 4.6%, ranging from 0.20 in winter to a peak of 18.6% during the spring bloom. This study confirms that respiration is an important fate for C in the Amundsen Gulf, and our rate‐based estimates of ecosystem scale CR suggests that considerably more C is respired than could be accounted for by gross primary production (GPP). One of the most plausible explanations for this observed discrepancy is that regenerated primary production is currently underestimated.</abstract>
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<note type="content"> Auxiliary material for this article contains a figure, a table, and a short discussion describing the potential effect of temperature correction on respiration rates. Auxiliary material files may require downloading to a local drive depending on platform, browser, configuration, and size. To open auxiliary materials in a browser, click on the label. To download, Right‐click and select “Save Target As…” (PC) or CTRL‐click and select “Download Link to Disk” (Mac). Additional file information is provided in the readme.txt. Auxiliary material for this article contains a figure, a table, and a short discussion describing the potential effect of temperature correction on respiration rates. Auxiliary material files may require downloading to a local drive depending on platform, browser, configuration, and size. To open auxiliary materials in a browser, click on the label. To download, Right‐click and select “Save Target As…” (PC) or CTRL‐click and select “Download Link to Disk” (Mac). Additional file information is provided in the readme.txt. Auxiliary material for this article contains a figure, a table, and a short discussion describing the potential effect of temperature correction on respiration rates. Auxiliary material files may require downloading to a local drive depending on platform, browser, configuration, and size. To open auxiliary materials in a browser, click on the label. To download, Right‐click and select “Save Target As…” (PC) or CTRL‐click and select “Download Link to Disk” (Mac). Additional file information is provided in the readme.txt.Supporting Info Item: readme.txt - Text S1. A short discussion of the supplementary information given to the reader. - Figure S1. Caption: Comparison of the uncorrected (crosses) and CR corrected with a Q10 of 4 (open circles)as per the manuscript as a function of in situ temperature. - Table S1. Comparison of uncorrected and corrected CR estimates using Q10 values of 2 and 4, within situ and incubation temperature, geographical localization, and depth sampled. - Tab‐delimited Table 1. - Tab‐delimited Table 2. - Tab‐delimited Table 3. - </note>
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