2011
DOI: 10.1007/s10592-011-0295-9
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Species designation of the Bruneau Dune tiger beetle (Cicindela waynei) is supported by phylogenetic analysis of mitochondrial DNA sequence data

Abstract: Beetles comprise nearly one quarter of described species and show high levels of morphological and ecological diversification. Because of their wide distribution, ease of detection, and correlation of species richness patterns with other taxa, tiger beetles have been recommended for use as a global indicator of regional biodiversity, requiring accurate taxonomic designations. The Bruneau Dune tiger beetle (Cicindela waynei), whose habitat consists of an isolated dune field in southern Idaho, was recently descr… Show more

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Cited by 3 publications
(2 citation statements)
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“…Uncorrelated morphological and genetic diversity has been reported in lyponiine lycids (Li et al 2015) and other beetle families (e.g. Goldberg et al 2012) and points to the necessary evaluation of all evidence when species are delimited (Jorger and Schrodl 2013). The cox1 mtDNA fragment alone cannot provide sufficient information on the diversification process, but even these limited data suggest that closely related lineages can develop distant mimetic patterns and start further morphological differentiation, for example in the relative size of eyes.…”
Section: Discussionmentioning
confidence: 99%
“…Uncorrelated morphological and genetic diversity has been reported in lyponiine lycids (Li et al 2015) and other beetle families (e.g. Goldberg et al 2012) and points to the necessary evaluation of all evidence when species are delimited (Jorger and Schrodl 2013). The cox1 mtDNA fragment alone cannot provide sufficient information on the diversification process, but even these limited data suggest that closely related lineages can develop distant mimetic patterns and start further morphological differentiation, for example in the relative size of eyes.…”
Section: Discussionmentioning
confidence: 99%
“…The advancement of molecular‐based delimitation approaches through the incorporation of coalescent theory (e.g., Knowles & Carstens, ; O'Meara, ; Pons et al., ; Yang & Rannala, ) has represented a huge step forward in our ability to robustly delimit species, especially at recent timescales. The past 10 years have seen an explosion in molecular species delimitation approaches (e.g., Camargo, Morando, Avila, & Sites, ; Ence & Carstens, ; Grummer, Bryson, & Reeder, ; Knowles & Carstens, ; O'Meara, ; Pons et al., ; Solís‐Lemus, Knowles, & Ané, ; Yang & Rannala, ), empirical examples (e.g., Goldberg et al., ; Reeves & Richards, ; Satler, Carstens, & Hedin, ; Singh et al., ) and critical reviews (e.g., Camargo et al., ; Carstens et al., ; Leaché & Fujita, ). Most authors agree that the use of multiple lines of evidence (Schlick‐Steiner et al., ; Yeates et al., ), multiple approaches in conjunction (Aguilar et al., ; Andújar, Arribas, Ruiz, Serrano, & Gómez‐Zurita, ; Fujita, Leaché, Burbrink, McGuire, & Moritz, ), and when possible, integrated analyses (Edwards & Knowles, ; Guillot, Renaud, Ledevin, Michaux, & Claude, ; Padial, Miralles, la Riva, & Vences, ; Zapata & Jiménez, ), are necessary to be objective in our delimitations.…”
Section: Introductionmentioning
confidence: 99%