2011
DOI: 10.1007/s10841-011-9377-8
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Conservation genetics of xerothermic beetles in Europe: the case of Centricnemus leucogrammus

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Cited by 17 publications
(30 citation statements)
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References 51 publications
(49 reference statements)
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“…The diversity of the nuclear EF1‐α gene is low in P. inustus , but this gene has only one single variant in E. ovulum . The interpretation of these results needs a broader context, eg through comparison with some sexual species such as the weevil Centricnemus leucogrammus , which also belongs to Entiminae and inhabits steppes (Kajtoch & Lachowska‐Cierlik, ; Kajtoch, ). This species has much higher genetic diversity in both mitochondrial and nuclear DNA (nucDNA), which supports the statement that parthenogenetic weevils have reduced genetic diversity compared with bisexual species.…”
Section: Discussionmentioning
confidence: 99%
“…The diversity of the nuclear EF1‐α gene is low in P. inustus , but this gene has only one single variant in E. ovulum . The interpretation of these results needs a broader context, eg through comparison with some sexual species such as the weevil Centricnemus leucogrammus , which also belongs to Entiminae and inhabits steppes (Kajtoch & Lachowska‐Cierlik, ; Kajtoch, ). This species has much higher genetic diversity in both mitochondrial and nuclear DNA (nucDNA), which supports the statement that parthenogenetic weevils have reduced genetic diversity compared with bisexual species.…”
Section: Discussionmentioning
confidence: 99%
“…The concentration of the reactives used for the amplifications and the cycling profiles for the polymerase chain reaction (PCR) of COII, ITS2 and EF1‐α markers were as in Kajtoch et al . (2009) and Kajtoch (2011). Wolbachia genes were screened as in Lachowska et al .…”
Section: Methodsmentioning
confidence: 99%
“…Additionally, EF1-α and Internal Transcribed Spacer 1 (ITS1) nuclear markers, also frequently used in phylogenetic studies of insects, were amplified using primer pairs EFs149 and EFα1R [30,31] and ITS1 and ITS2 [32]. The concentration of the reagents used for the amplification of COI, ITS1 and EF1-α markers and the cycling profile for PCR have been described previously [33,34]. After purification (NucleoSpin Extract II, Macherey-Nagel), the PCR fragments were sequenced using a BigDye Terminator v.3.1.…”
Section: Laboratory Proceduresmentioning
confidence: 99%