2011
DOI: 10.1038/ismej.2011.184
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Freshwater bacterioplankton richness in oligotrophic lakes depends on nutrient availability rather than on species–area relationships

Abstract: A central goal in ecology is to grasp the mechanisms that underlie and maintain biodiversity and patterns in its spatial distribution can provide clues about those mechanisms. Here, we investigated what might determine the bacterioplankton richness (BR) in lakes by means of 454 pyrosequencing of the 16S rRNA gene. We further provide a BR estimate based upon a sampling depth and accuracy, which, to our knowledge, are unsurpassed for freshwater bacterioplankton communities. Our examination of 22 669 sequences pe… Show more

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Cited by 94 publications
(75 citation statements)
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“…The factors that shape this bacterial diversity and in turn how the bacterial community contributes to ecosystem functioning have become a subject of intense research. The variability in bacterial community structure on different temporal and spatial scales has been shown to correlate with changes in biotic and abiotic environmental factors, indicating their selective control of bacterial communities (Ramette 2007, Logue et al 2012. These studies have further provided insight into the co-occurrence of different phylotypes, suggesting environmentally driven interactions among bacterial groups (Fuhrman et al 2006, Gilbert et al 2012.…”
Section: Introductionmentioning
confidence: 84%
“…The factors that shape this bacterial diversity and in turn how the bacterial community contributes to ecosystem functioning have become a subject of intense research. The variability in bacterial community structure on different temporal and spatial scales has been shown to correlate with changes in biotic and abiotic environmental factors, indicating their selective control of bacterial communities (Ramette 2007, Logue et al 2012. These studies have further provided insight into the co-occurrence of different phylotypes, suggesting environmentally driven interactions among bacterial groups (Fuhrman et al 2006, Gilbert et al 2012.…”
Section: Introductionmentioning
confidence: 84%
“…Samples without reverse transcriptase and with MilliQ water instead of target RNA served as negative controls. The hypervariable regions V3 and V4 of the bacterial 16S rRNA gene were PCR amplified using the barcoded forward primer 341F (5=-CCTACGGGNGGCWGCAG-3=) and the reverse primer 805R (5=-GACTACHVGGGTATCTAATCC-3=) (27). For each sample, two different bar codes were used to reduce bar code-specific bias (28).…”
Section: Methodsmentioning
confidence: 99%
“…Each PCR reaction included a negative control. Primers used for amplification of the 16S rRNA gene were the bacterial 341F 5′-CCTACGG GNGGCWGCAG-3′ and 805R 5′-GACTACHVGGGTA TCTAATCC-3′, containing the 454 Titanium A and B adaptors, respectively (Logue et al, 2011). For each sample, two different sample-specific barcodes contained in the forward primer were used to reduce barcode-specific bias (Berry et al, 2011).…”
Section: Pcr Amplification and 454 Pyrosequencingmentioning
confidence: 99%