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Microbial food web structure in a naturally iron-fertilized area in the Southern Ocean (Kerguelen Plateau)

Identifieur interne : 003072 ( PascalFrancis/Checkpoint ); précédent : 003071; suivant : 003073

Microbial food web structure in a naturally iron-fertilized area in the Southern Ocean (Kerguelen Plateau)

Auteurs : U. Christaki [France] ; I. Obernosterer [France] ; F. Van Wambeke [France] ; M. Veldhuis [Pays-Bas] ; N. Garcia [France] ; P. Catala [France]

Source :

RBID : Pascal:08-0300421

Descripteurs français

English descriptors

Abstract

The objective of this study in the framework of the KErguelen Ocean and Plateau compared Study, 2005-2007 (KEOPS) project was to examine the microbial food web structure within a phytoplankton bloom induced by natural iron fertilization. Integrated bacterial production (BP, 0-100 m) varied 12-fold over the study area (23.5-304 mg C m-2 d-1), while bacterial abundance (0-100 m) varied only by a factor of 2.8. Highest bacterial abundances and rates of BP were observed in the center of the diatom-dominated bloom, and substantial decreases in BP towards the later bloom stage were detectable. The abundance of bacterial predators (heterotrophic nanoflagellates, HNF) showed a significant coupling with BP in the high-nutrient low-chlorophyll (HNLC) area only. In the core of the bloom, BP consumed by HNF was 27 %, 29%, 52% and 34% during the four consecutive visits that extended over 4 weeks and was much higher (80-95%) in HNLC waters. The relative contribution of the small-sized (< 10 μm) phytoplankton in terms of chlorophyll was only minor within bloom. Ciliated protozoa showed low abundance (20-556 cells l-1) all over the studied area; however, in terms of biomass ciliates were more important within (224 mg C m-2, 0-lOOm) than outside the bloom (30.5 mg C m-2, 0-100m). This difference was attributable mainly to tintinnids Cymatocyclis spp. accounting for 30-80% of the total ciliate biomass within the Kerguelen bloom but being rare in the HNLC water. Mixotrophic ciliate biomass accounted for 40-60% of the total aloricate ciliate biomass all over the studied area. This was mainly due to the relatively large size of mixotrophic ciliates present in the samples (Tontonia antarctica, Strombidium spp. and Laboea strobila). Overall, our results suggest a strong response of bacteria, weak response of HNF, and strong controlling effects on ciliates. The weak coupling between heterotrophic bacteria and HNF and the low abundance of ciliates suggest a low transfer of carbon from the microbial to the classical food web within the Kerguelen bloom.


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<div type="abstract" xml:lang="en">The objective of this study in the framework of the KErguelen Ocean and Plateau compared Study, 2005-2007 (KEOPS) project was to examine the microbial food web structure within a phytoplankton bloom induced by natural iron fertilization. Integrated bacterial production (BP, 0-100 m) varied 12-fold over the study area (23.5-304 mg C m
<sup>-2</sup>
d
<sup>-1</sup>
), while bacterial abundance (0-100 m) varied only by a factor of 2.8. Highest bacterial abundances and rates of BP were observed in the center of the diatom-dominated bloom, and substantial decreases in BP towards the later bloom stage were detectable. The abundance of bacterial predators (heterotrophic nanoflagellates, HNF) showed a significant coupling with BP in the high-nutrient low-chlorophyll (HNLC) area only. In the core of the bloom, BP consumed by HNF was 27 %, 29%, 52% and 34% during the four consecutive visits that extended over 4 weeks and was much higher (80-95%) in HNLC waters. The relative contribution of the small-sized (< 10 μm) phytoplankton in terms of chlorophyll was only minor within bloom. Ciliated protozoa showed low abundance (20-556 cells l
<sup>-1</sup>
) all over the studied area; however, in terms of biomass ciliates were more important within (224 mg C m
<sup>-2</sup>
, 0-lOOm) than outside the bloom (30.5 mg C m
<sup>-2</sup>
, 0-100m). This difference was attributable mainly to tintinnids Cymatocyclis spp. accounting for 30-80% of the total ciliate biomass within the Kerguelen bloom but being rare in the HNLC water. Mixotrophic ciliate biomass accounted for 40-60% of the total aloricate ciliate biomass all over the studied area. This was mainly due to the relatively large size of mixotrophic ciliates present in the samples (Tontonia antarctica, Strombidium spp. and Laboea strobila). Overall, our results suggest a strong response of bacteria, weak response of HNF, and strong controlling effects on ciliates. The weak coupling between heterotrophic bacteria and HNF and the low abundance of ciliates suggest a low transfer of carbon from the microbial to the classical food web within the Kerguelen bloom.</div>
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<s0>The objective of this study in the framework of the KErguelen Ocean and Plateau compared Study, 2005-2007 (KEOPS) project was to examine the microbial food web structure within a phytoplankton bloom induced by natural iron fertilization. Integrated bacterial production (BP, 0-100 m) varied 12-fold over the study area (23.5-304 mg C m
<sup>-2</sup>
d
<sup>-1</sup>
), while bacterial abundance (0-100 m) varied only by a factor of 2.8. Highest bacterial abundances and rates of BP were observed in the center of the diatom-dominated bloom, and substantial decreases in BP towards the later bloom stage were detectable. The abundance of bacterial predators (heterotrophic nanoflagellates, HNF) showed a significant coupling with BP in the high-nutrient low-chlorophyll (HNLC) area only. In the core of the bloom, BP consumed by HNF was 27 %, 29%, 52% and 34% during the four consecutive visits that extended over 4 weeks and was much higher (80-95%) in HNLC waters. The relative contribution of the small-sized (< 10 μm) phytoplankton in terms of chlorophyll was only minor within bloom. Ciliated protozoa showed low abundance (20-556 cells l
<sup>-1</sup>
) all over the studied area; however, in terms of biomass ciliates were more important within (224 mg C m
<sup>-2</sup>
, 0-lOOm) than outside the bloom (30.5 mg C m
<sup>-2</sup>
, 0-100m). This difference was attributable mainly to tintinnids Cymatocyclis spp. accounting for 30-80% of the total ciliate biomass within the Kerguelen bloom but being rare in the HNLC water. Mixotrophic ciliate biomass accounted for 40-60% of the total aloricate ciliate biomass all over the studied area. This was mainly due to the relatively large size of mixotrophic ciliates present in the samples (Tontonia antarctica, Strombidium spp. and Laboea strobila). Overall, our results suggest a strong response of bacteria, weak response of HNF, and strong controlling effects on ciliates. The weak coupling between heterotrophic bacteria and HNF and the low abundance of ciliates suggest a low transfer of carbon from the microbial to the classical food web within the Kerguelen bloom.</s0>
</fC01>
<fC02 i1="01" i2="2">
<s0>001E02B</s0>
</fC02>
<fC02 i1="02" i2="2">
<s0>001E01P02</s0>
</fC02>
<fC02 i1="03" i2="2">
<s0>001E01H</s0>
</fC02>
<fC02 i1="04" i2="2">
<s0>226C02</s0>
</fC02>
<fC02 i1="05" i2="2">
<s0>223B</s0>
</fC02>
<fC03 i1="01" i2="2" l="FRE">
<s0>Fer</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="2" l="ENG">
<s0>iron</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="2" l="SPA">
<s0>Hierro</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="2" l="FRE">
<s0>Océan Antarctique</s0>
<s2>564</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="2" l="ENG">
<s0>Antarctic Ocean</s0>
<s2>564</s2>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="2" l="FRE">
<s0>Bâti</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="2" l="ENG">
<s0>frame structure</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="2" l="FRE">
<s0>Projet</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="2" l="ENG">
<s0>projects</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="2" l="SPA">
<s0>Proyecto</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="2" l="FRE">
<s0>Phytoplancton</s0>
<s2>NY</s2>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="2" l="ENG">
<s0>phytoplankton</s0>
<s2>NY</s2>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="2" l="SPA">
<s0>Fitoplancton</s0>
<s2>NY</s2>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="2" l="FRE">
<s0>Fertilisation</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="2" l="ENG">
<s0>fertilization</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="2" l="SPA">
<s0>Fertilización</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="2" l="FRE">
<s0>Pli</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="2" l="ENG">
<s0>folds</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="2" l="SPA">
<s0>Pliegue</s0>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="2" l="FRE">
<s0>Abondance</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="2" l="ENG">
<s0>abundance</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="2" l="SPA">
<s0>Abundancia</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="2" l="FRE">
<s0>Diatomeae</s0>
<s2>NY</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="2" l="ENG">
<s0>diatoms</s0>
<s2>NY</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="2" l="SPA">
<s0>Diatomea</s0>
<s2>NY</s2>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="2" l="FRE">
<s0>Prédateur</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="2" l="ENG">
<s0>predators</s0>
<s5>10</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Couplage faible</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Weak coupling</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Acoplamiento débil</s0>
<s5>11</s5>
</fC03>
<fC03 i1="12" i2="2" l="FRE">
<s0>Elément nutritif</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="2" l="ENG">
<s0>nutrients</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="2" l="SPA">
<s0>Nutriente</s0>
<s5>12</s5>
</fC03>
<fC03 i1="13" i2="2" l="FRE">
<s0>Chlorophylle</s0>
<s5>14</s5>
</fC03>
<fC03 i1="13" i2="2" l="ENG">
<s0>chlorophyll</s0>
<s5>14</s5>
</fC03>
<fC03 i1="13" i2="2" l="SPA">
<s0>Clorofila</s0>
<s5>14</s5>
</fC03>
<fC03 i1="14" i2="2" l="FRE">
<s0>Carotte</s0>
<s5>15</s5>
</fC03>
<fC03 i1="14" i2="2" l="ENG">
<s0>drill cores</s0>
<s5>15</s5>
</fC03>
<fC03 i1="14" i2="2" l="SPA">
<s0>Testigo</s0>
<s5>15</s5>
</fC03>
<fC03 i1="15" i2="2" l="FRE">
<s0>Protozoa</s0>
<s5>16</s5>
</fC03>
<fC03 i1="15" i2="2" l="ENG">
<s0>Protozoa</s0>
<s5>16</s5>
</fC03>
<fC03 i1="15" i2="2" l="SPA">
<s0>Protozoa</s0>
<s5>16</s5>
</fC03>
<fC03 i1="16" i2="2" l="FRE">
<s0>Biomasse</s0>
<s5>17</s5>
</fC03>
<fC03 i1="16" i2="2" l="ENG">
<s0>biomass</s0>
<s5>17</s5>
</fC03>
<fC03 i1="16" i2="2" l="SPA">
<s0>Biomasa</s0>
<s5>17</s5>
</fC03>
<fC03 i1="17" i2="2" l="FRE">
<s0>Bactérie</s0>
<s2>NY</s2>
<s5>18</s5>
</fC03>
<fC03 i1="17" i2="2" l="ENG">
<s0>bacteria</s0>
<s2>NY</s2>
<s5>18</s5>
</fC03>
<fC03 i1="18" i2="2" l="FRE">
<s0>Carbone</s0>
<s5>19</s5>
</fC03>
<fC03 i1="18" i2="2" l="ENG">
<s0>carbon</s0>
<s5>19</s5>
</fC03>
<fC03 i1="18" i2="2" l="SPA">
<s0>Carbono</s0>
<s5>19</s5>
</fC03>
<fC03 i1="19" i2="2" l="FRE">
<s0>Plateau Kerguelen</s0>
<s2>NG</s2>
<s5>61</s5>
</fC03>
<fC03 i1="19" i2="2" l="ENG">
<s0>Kerguelen Plateau</s0>
<s2>NG</s2>
<s5>61</s5>
</fC03>
<fC03 i1="20" i2="2" l="FRE">
<s0>Antarctique</s0>
<s2>NG</s2>
<s5>62</s5>
</fC03>
<fC03 i1="20" i2="2" l="ENG">
<s0>Antarctica</s0>
<s2>NG</s2>
<s5>62</s5>
</fC03>
<fC03 i1="20" i2="2" l="SPA">
<s0>Antártico</s0>
<s2>NG</s2>
<s5>62</s5>
</fC03>
<fC07 i1="01" i2="2" l="FRE">
<s0>Plancton</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="01" i2="2" l="ENG">
<s0>plankton</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="01" i2="2" l="SPA">
<s0>Plancton</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="02" i2="2" l="FRE">
<s0>Algae</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="02" i2="2" l="ENG">
<s0>algae</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="02" i2="2" l="SPA">
<s0>Algae</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="03" i2="2" l="FRE">
<s0>Thallophyta</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="03" i2="2" l="ENG">
<s0>Thallophyta</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="03" i2="2" l="SPA">
<s0>Thallophyta</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="04" i2="2" l="FRE">
<s0>Plantae</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="04" i2="2" l="ENG">
<s0>Plantae</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="05" i2="2" l="FRE">
<s0>Procaryote</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="05" i2="2" l="ENG">
<s0>prokaryotes</s0>
<s2>NY</s2>
</fC07>
<fC07 i1="06" i2="2" l="FRE">
<s0>Océan Indien</s0>
<s2>564</s2>
</fC07>
<fC07 i1="06" i2="2" l="ENG">
<s0>Indian Ocean</s0>
<s2>564</s2>
</fC07>
<fC07 i1="06" i2="2" l="SPA">
<s0>Océano Indico</s0>
<s2>564</s2>
</fC07>
<fC07 i1="07" i2="2" l="FRE">
<s0>Région Polaire</s0>
<s2>564</s2>
</fC07>
<fC07 i1="07" i2="2" l="ENG">
<s0>polar regions</s0>
<s2>564</s2>
</fC07>
<fN21>
<s1>189</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
<affiliations>
<list>
<country>
<li>France</li>
<li>Pays-Bas</li>
</country>
<region>
<li>Hauts-de-France</li>
<li>Languedoc-Roussillon</li>
<li>Nord-Pas-de-Calais</li>
<li>Occitanie (région administrative)</li>
<li>Provence-Alpes-Côte d'Azur</li>
</region>
<settlement>
<li>Banyuls-sur-Mer</li>
<li>Marseille</li>
<li>Wimereux</li>
</settlement>
<orgName>
<li>Université de la Méditerranée</li>
</orgName>
</list>
<tree>
<country name="France">
<region name="Hauts-de-France">
<name sortKey="Christaki, U" sort="Christaki, U" uniqKey="Christaki U" first="U." last="Christaki">U. Christaki</name>
</region>
<name sortKey="Catala, P" sort="Catala, P" uniqKey="Catala P" first="P." last="Catala">P. Catala</name>
<name sortKey="Garcia, N" sort="Garcia, N" uniqKey="Garcia N" first="N." last="Garcia">N. Garcia</name>
<name sortKey="Obernosterer, I" sort="Obernosterer, I" uniqKey="Obernosterer I" first="I." last="Obernosterer">I. Obernosterer</name>
<name sortKey="Van Wambeke, F" sort="Van Wambeke, F" uniqKey="Van Wambeke F" first="F." last="Van Wambeke">F. Van Wambeke</name>
</country>
<country name="Pays-Bas">
<noRegion>
<name sortKey="Veldhuis, M" sort="Veldhuis, M" uniqKey="Veldhuis M" first="M." last="Veldhuis">M. Veldhuis</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

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   |wiki=    Wicri/Asie
   |area=    AustralieFrV1
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   |texte=   Microbial food web structure in a naturally iron-fertilized area in the Southern Ocean (Kerguelen Plateau)
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