scholarly journals Molecular divergence among Yellow-spotted Barbet Buccanodon duchaillui populations suggests unrecognised diversity

2021 ◽  
Vol 141 (3) ◽  
Author(s):  
Brooks C. Hall ◽  
Lucas H. DeCicco ◽  
Isaac N. Rush ◽  
Emily N. Ostrow ◽  
Robert G. Moyle
Keyword(s):  
1979 ◽  
Vol 57 (5) ◽  
pp. 979-982 ◽  
Author(s):  
Emmanuel C. Igbokwe

Species-specific patterns of larval protein electrophoregrams obtained among three species of Aedes mosquitoes were analyzed numerically. A behavioral profile was derived and illustrated for the larval protein complex of each species. Patterns of interspecific divergence in molecular behavior not detectable otherwise from the electrophoregrams were evident in the behavioral profiles of the proteins. The degree of electrophoretic correspondence obtained from the number of shared fractions among the species differs from that derived from the collective behavior of proteins. The numerical and graphic approach to the interpretation of protein electrophoregrams offers another parameter for gauging molecular divergence among related species of insects.


2007 ◽  
Vol 30 (2) ◽  
pp. 109-118 ◽  
Author(s):  
Erko Stackebrandt ◽  
Orsola Päuker ◽  
Ulrike Steiner ◽  
Peter Schumann ◽  
Bettina Sträubler ◽  
...  

2016 ◽  
Vol 64 ◽  
pp. 38-45 ◽  
Author(s):  
Vanessa Neves de Azevedo Fernandes ◽  
Andréa Florindo das Neves ◽  
Paula Garcia Martin ◽  
Claudete Aparecida Mangolin ◽  
Maria de Fátima P.S. Machado

Author(s):  
Richard Holmquist ◽  
Thomas H. Jukes ◽  
Dennis Pearl
Keyword(s):  

2014 ◽  
Vol 281 (1788) ◽  
pp. 20140677 ◽  
Author(s):  
Daniel T. Ksepka ◽  
Jessica L. Ware ◽  
Kristin S. Lamm

Major disparities are recognized between molecular divergence dates and fossil ages for critical nodes in the Tree of Life, but broad patterns and underlying drivers remain elusive. We harvested 458 molecular age estimates for the stem and crown divergences of 67 avian clades to explore empirical patterns between these alternate sources of temporal information. These divergence estimates were, on average, over twice the age of the oldest fossil in these clades. Mitochondrial studies yielded older ages than nuclear studies for the vast majority of clades. Unexpectedly, disparity between molecular estimates and the fossil record was higher for divergences within major clades (crown divergences) than divergences between major clades (stem divergences). Comparisons of dates from studies classed by analytical methods revealed few significant differences. Because true divergence ages can never be known with certainty, our study does not answer the question of whether fossil gaps or molecular dating error account for a greater proportion of observed disparity. However, empirical patterns observed here suggest systemic overestimates for shallow nodes in existing molecular divergence dates for birds. We discuss underlying biases that may drive these patterns.


2009 ◽  
Vol 11 (4) ◽  
pp. 1283-1298 ◽  
Author(s):  
Eric A. VanderWerf ◽  
Lindsay C. Young ◽  
Norine W. Yeung ◽  
David B. Carlon

2013 ◽  
Vol 26 (6) ◽  
pp. 408 ◽  
Author(s):  
Matt A. M. Renner ◽  
Nicolas Devos ◽  
Elizabeth A. Brown ◽  
Matt J. von Konrat

The current paper presents molecular data from three chloroplast markers (atpB–rbcL spacer, trnG G2 intron, trnL–trnF intron and spacer); morphological data, and geographic data to support the recognition of nine species belonging to Radula subg. Odontoradula in Australasia. R. ocellata, the subgeneric type from the Wet Tropics bioregion, is maintained as distinct from its sister species, R. pulchella, from south-eastern Australian rainforests; both species are Australian endemics. Reinstatement of R. allisonii from synonymy, under R. retroflexa, is supported by molecular data and morphological characters, including the absence of triradiate trigones on leaf-lobe cell walls, the apex of lobules on primary shoots not being turned outwards, the oblong-elliptic female bracts, and the perianths having a pronounced wing. Reinstatement of R. weymouthiana, from synonymy under R. retroflexa, is also supported by molecular data and morphological characters, including the presence of a single low dome-shaped papilla over each leaf-lobe cell, and the large imbricate lobules on primary shoots. R. weymouthiana occurs in Tasmania and New Zealand, whereas R. allisonii is a New Zealand endemic. Australian R. retroflexa exhibits differentiation into epiphytic and rheophytic morphs, interpreted as ecotypes. Australian individuals, comprising both epiphytic and rheophytic morphs, are monophyletic and nested within a clade containing individuals from other regions. R. novae-hollandiae is newly reported for the New Zealand Botanical Region, from Raoul Island in the Kermadecs. R. novae-hollandiae exhibits decoupling of morphological and molecular divergence, with Australian individuals forming two clades reflecting geography (a Wet Tropics bioregion clade and a south-eastern Rainforest clade). These clades exhibit equivalent levels of molecular divergence, as observed in R. pulchella and R. ocellata, but no morphological differences. Similar levels of molecular divergence were observed in trans-Tasman populations of R. tasmanica. The New Zealand endemic, R. plicata, is excluded from the Australian flora, and R. cuspidata replaces R. dentifolia for the New Zealand endemic species formerly known by both names.


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