2010
DOI: 10.3354/ame01399
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Vertical distribution of planktonic autotrophic thiobacilli and dark CO2 fixation rates in lakes with oxygen–sulfide interfaces

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Cited by 18 publications
(18 citation statements)
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References 48 publications
(63 reference statements)
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“…Thus, essentially all microorganisms can assimilate CO 2 in any step of their metabolism, but the maximal activity should be expected at the oxic-anoxic interface where the true specialists may develop. However, as a whole, we did not find any significant correlation between these rates and either nutrient distribution or microbial community composition in the study lakes and in other similar lakes reported elsewhere (García-Cantizano et al 2005, Casamayor 2010). This may indicate that different physiologies and ecologies may simultaneously contribute in situ to the dark carbon fixation activity of these ecosystems.…”
Section: Discussioncontrasting
confidence: 39%
“…Thus, essentially all microorganisms can assimilate CO 2 in any step of their metabolism, but the maximal activity should be expected at the oxic-anoxic interface where the true specialists may develop. However, as a whole, we did not find any significant correlation between these rates and either nutrient distribution or microbial community composition in the study lakes and in other similar lakes reported elsewhere (García-Cantizano et al 2005, Casamayor 2010). This may indicate that different physiologies and ecologies may simultaneously contribute in situ to the dark carbon fixation activity of these ecosystems.…”
Section: Discussioncontrasting
confidence: 39%
“…Sulfurimonas (Grote et al , 2007, 2008)], and the aerobic sulfur‐oxidizing bacteria [e.g. Thiobacilli (Casamayor, 2010)]. However, the capability of lacustrine archaea other than ammonia oxidizers to incorporate CO 2 in the dark has not been assessed in aquatic environments with well‐defined oxic/anoxic interfaces.…”
Section: Discussionmentioning
confidence: 99%
“…In some of these habitats, the values of dark fixation rates integrated for the entire water column were equivalent to those calculated for light‐driven processes, indicating that dark assimilation could not be easily disregarded. Besides, the complexity of the microbial assemblages thriving in environments with oxic/anoxic interfaces and the availability of different energy sources and electron donors favor the presence of a large diversity of microorganisms involved in chemoautotrophic activities (Casamayor, 2010).…”
Section: Introductionmentioning
confidence: 99%
“…4 and 6). Despite the apparent vertical and seasonal pattern, most previous studies found weak or no correlation between chemoautotrophy and geochemical variables presumably due to the coexistence of a diverse assemblage of physiological and ecological types of chemoautotrophs (Casamayor, 2010;Casamayor et al, 2012). However, we found significant models with a gradient of some geochemical variables, including density, DO, DS, DFe, and Table 1 Correlation matrix of biogeochemical values at different depths (lower left) and gradients across neighboring depths (upper right) during the temporal and transect survey (n ¼ 88).…”
Section: Chemoautotrophymentioning
confidence: 91%
“…One of best-studied examples of microbial diversity are active chemoautotrophic and anoxygenic photoautotrophic processes attributed to the simultaneous presence of various oxidized and reduced compounds. The vertical distribution of the microbes is strongly related to the vertical structure of oxic/anoxic or oxic/sulfidic interfaces (Sorokin et al, 1995;Casamayor, 2010;Casamayor et al, 2012). In some ecosystems where photosynthetic production is restricted to upper mixed layers, chemoautotrophic production can support a deep secondary microbial food web (Ho et al, 2004;Alonso-S aez et al, 2010;Swan et al, 2011).…”
Section: Introductionmentioning
confidence: 99%