2015
DOI: 10.1071/is14021
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A multigene phylogenetic analysis results in a redefinition of the genus Notonomus Chaudoir (Coleoptera, Carabidae) and descriptions of new species of the subgenus Leiradira Castelnau

Kipling Will

Abstract: Bayesian analysis of four partial gene sequences (28S rDNA, wg, CAD and COI mtDNA) from exemplars of all genera and 12 of 17 informal groups of the Notonomus-series of pterostichine carabids strongly supports a clade requiring redefinition of Notonomus Chaudoir, 1862. Notonomus is redefined to include all species currently placed in Notonomus by Lorenz (2005a) plus two Sarticus Motschulsky, 1865 species (S. blackburni (Sloane, 1895) and S. impar (Sloane, 1893)), all species of Leiradira Castelnau, 1867, Conchi… Show more

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“…Abbreviations used for loci and their aligned length in the matrices are as follows: 28S: 28S ribosomal DNA (1297bp); COI: cytochrome oxidase I, (851bp, JER-PAT primer region (COIjp), 707bp, HCO-LCO region (COIf)); wg: wingless (529bp); CAD2: carbamoyl phosphate synthetase domain of the rudimentary gene (931bp). Fragments for these genes were amplified using polymerase chain reaction, exo-sap cleaned and sequenced following the same procedures and primers given by Will (2015a). Assembly of multiple chromatograms for each gene fragment and initial base calls were made with Phred (Green and Ewing 2002) and Phrap (Green 1999) initiated within Mesquite's (Maddison and Maddison 2018b) Chromaseq package (Maddison and Maddison 2019) with subsequent editing done by manual inspection within Mesquite.…”
Section: Dna Sequencingmentioning
confidence: 99%
“…Abbreviations used for loci and their aligned length in the matrices are as follows: 28S: 28S ribosomal DNA (1297bp); COI: cytochrome oxidase I, (851bp, JER-PAT primer region (COIjp), 707bp, HCO-LCO region (COIf)); wg: wingless (529bp); CAD2: carbamoyl phosphate synthetase domain of the rudimentary gene (931bp). Fragments for these genes were amplified using polymerase chain reaction, exo-sap cleaned and sequenced following the same procedures and primers given by Will (2015a). Assembly of multiple chromatograms for each gene fragment and initial base calls were made with Phred (Green and Ewing 2002) and Phrap (Green 1999) initiated within Mesquite's (Maddison and Maddison 2018b) Chromaseq package (Maddison and Maddison 2019) with subsequent editing done by manual inspection within Mesquite.…”
Section: Dna Sequencingmentioning
confidence: 99%
“…Methods and terms follow Will (2011;2015). Material examined is housed in the following collections and listed using these coden:…”
Section: Methodsmentioning
confidence: 99%