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Phylogenetic studies by Korall & Kenrick determined that the Euselaginella group, comprising solely the type species, Selaginella selaginoides and a closely related Hawai ' ian species, Selaginella deflexa, is a basal and anciently diverging sister to all other Selaginella species.
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Phylogenetic and studies
Phylogenetic studies have not indicated a correlation between evolution of Sodalis and tsetse.
Phylogenetic studies generally have shown the clouded leopard ( Neofelis nebulosa ) is basal to this group.
Phylogenetic studies indicate that Shigella is more appropriately treated as subgenus of Escherichia, and that certain strains generally considered E. coli – such as E. coli O157: H7 – are better placed in Shigella ( see Escherichia coli # Diversity for details ).
Phylogenetic studies suggest an African origin for this pathogen.
Phylogenetic studies using mtDNA suggest that some morphological features have evolved more than once including the back and chin colour.
Phylogenetic studies suggest the true tanagers form three main groups two of which consist of several smaller, well-supported clades.
Phylogenetic studies strongly suggest that PVs normally evolve together with their mammalian and bird host species, do not change host species, do not recombine, and have maintained their basic genomic organization for a period exceeding 100 million years.
Phylogenetic studies based on molecular evidence ( e. g. Pfosser and Speta 1999 ), suggested that, along with Camassia, Chlorogalum seemed to be most closely related to Agave and Anthericum.
Phylogenetic studies did not support the idea that NGMC 91 was a close relative of S. millenii.
Phylogenetic studies have demonstrated that this broadly defined Loganiaceae was a polyphyletic assemblage, and numerous genera have been removed from Loganiaceae to other families ( sometimes in other orders ), e. g., Gentianaceae, Gelsemiaceae, Plocospermataceae, Tetrachondraceae, Buddlejaceae, and Gesneriaceae.
Phylogenetic studies have also demonstrated that the ancestor of Androsace first appeared about 35 Mya ago and was most probably an annual species.
& Wallace, Robert S. ( 2004 ): Phylogenetic studies of Mammillaria ( Cactaceae )-insights from chloroplast sequence variation and hypothesis testing using the parametric bootstrap.
" Phylogenetic studies of Ophioglossaceae: evidence from rbcL and trnL-F plastid DNA sequences and morphology.
Phylogenetic studies and modern classification of the Pyraloidea ( Lepidoptera ).
Phylogenetic and by
Phylogenetic analyses place these genera into the following groups ( not all of these are considered amoeboid ( or " amoebas ") by all sources ):
Phylogenetic analysis by Chris Organ, Charles Nunn, Zarin Machanda, and Richard Wrangham suggests that cooking may have been invented as far back as 1. 8 million to 2. 3 million years ago.
Phylogenetic tree suggested by Haeckel ( 1866 )
* Sheldon, Frederick H .; McCracken, Kevin G. & Stuebing, Keeley D. ( 1995 ): Phylogenetic relationships of the zigzag heron ( Zebrilus undulatus ) and white-crested bittern ( Tigriornis leucolophus ) estimated by DNA-DNA hybridization.
* ( 2008 ): Genetic Divergences and Phylogenetic Relationships Among the Fejervarya limnocharis Complex in Thailand and Neighboring Countries Revealed by Mitochondrial and Nuclear Genes.
Phylogenetic Position of the Tubercle Bacilli within the Genus Mycobacterium The blue triangle corresponds to tubercle bacilli sequences that are identical or differing by a single nucleotide.
Phylogenetic trees built on each of the 8 segments show a consistent picture of 3 lineages, as illustrated by the HA tree shown in Figure 1.
Phylogenetic research by Kadereit et al.
" The Paraphyly of Osmunda is Confirmed by Phylogenetic Analyses of Seven Plastid Loci.
Phylogenetic and &
* Martínez Gómez, Juan E .; Barber, Bruian R. & Peterson, A. Townsend ( 2005 ): Phylogenetic position and generic placement of the Socorro Wren ( Thryomanes sissonii ).
* Moyle, Robert G. & Marks, Ben D. ( 2006 ): Phylogenetic relationships of the bulbuls ( Aves: Pycnonotidae ) based on mitochondrial and nuclear DNA sequence data.
* Thomassen, Henri A .; Tex, Robert-Jan ; de Bakker, Merijn A. G. & Povel, G. David E. ( 2005 ): Phylogenetic relationships amongst swifts and swiftlets: A multi locus approach.
Phylogenetic analyses have shown that mimids are most closely related to starlings ( Sibley & Monroe 1990, Zuccon et al.
; Seibold, I .; Bednarek, W .; Brüning, H .; Gaucher, P .; Ristow, D .; Scharlau, W .; Schmidl, D. & Wink, Michael ( 1994 ): Phylogenetic relationships among falcon species ( genus Falco ) according to DNA sequence variation of the cytochrome b gene.
* Irestedt, Martin ; Fjeldså, Jon & Ericson, Per G. P. ( 2004 ): Phylogenetic relationships of woodcreepers ( Aves: Dendrocolaptinae )-incongruence between molecular and morphological data.
* Irestedt, Martin ; Fjeldså, Jon & Ericson, Per G. P. ( 2004 ): Phylogenetic relationships of woodcreepers ( Aves: Dendrocolaptinae )-incongruence between molecular and morphological data.
& M Westerman ( 1996 ) " Molecular Perspectives on the Phylogenetic Affinities of Lyrebirds ( Menuridae ) and Treecreepers ( Climacteridae )".
* Heidrich, Petra ; Amengual, José F. & Wink, Michael ( 1998 ): Phylogenetic relationships in Mediterranean and North Atlantic shearwaters ( Aves: Procellariidae ) based on nucleotide sequences of mtDNA.
* Heidrich, Petra ; Amengual, José F. & Wink, Michael ( 1998 ): Phylogenetic relationships in Mediterranean and North Atlantic shearwaters ( Aves: Procellariidae ) based on nucleotide sequences of mtDNA.
; Seibold, I .; Bednarek, W .; Brüning, H .; Gaucher, P .; Ristow, D .; Scharlau, W .; Schmidl, D. & Wink, Michael ( 1994 ): Phylogenetic relationships among falcon species ( genus Falco ) according to DNA sequence variation of the cytochrome b gene.
* Price, Jordan J .; Johnson, Kevin, P .; Bush, Sarah H. & Clayton, Dale H. ( 2005 ): Phylogenetic relationships of the Papuan Swiftlet Aerodramus papuensis and implications for the evolution of avian echolocation.
* Thomassen, Henri A .; Tex, Robert-Jan ; Bakker, Merijn A. G. & Povel, G. David E. ( 2005 ): Phylogenetic relationships amongst swifts and swiftlets: A multi locus approach.
; Seibold, I .; Bednarek, W .; Brüning, H .; Gaucher, P .; Ristow, D .; Scharlau, W .; Schmidl, D. & Wink, Michael ( 1994 ): Phylogenetic relationships among falcon species ( genus Falco ) according to DNA sequence variation of the cytochrome b gene.
* Wink, Michael ; Sauer-Gürth, Hedi ; Ellis, David & Kenward, Robert ( 2004 ): Phylogenetic relationships in the Hierofalco complex ( Saker -, Gyr -, Lanner -, Laggar Falcon ).
; Seibold, I .; Bednarek, W .; Brüning, H .; Gaucher, P .; Ristow, D .; Scharlau, W .; Schmidl, D. & Wink, M. ( 1994 ): Phylogenetic relationships among falcon species ( genus Falco ) according to DNA sequence variation of the cytochrome b gene.
* Wink, M .; Döttlinger, H .; Nicholls, M. K. & Sauer-Gürth, H. ( 2000 ): Phylogenetic relationships between Black Shaheen ( Falco peregrinus peregrinator ), Red-naped Shaheen ( F. pelegrinoides babylonicus ) and Peregrines ( F. peregrinus ).
* Wink, M .; Sauer-Gürth, H .; Ellis, D. & Kenward, R. ( 2004 ): Phylogenetic relationships in the Hierofalco complex ( Saker -, Gyr -, Lanner -, Laggar Falcon ).
* Heidrich, Petra ; Amengual, José F. & Wink, Michael ( 1998 ): Phylogenetic relationships in Mediterranean and North Atlantic shearwaters ( Aves: Procellariidae ) based on nucleotide sequences of mtDNA.
; Seibold, I .; Bednarek, W .; Brüning, H .; Gaucher, P .; Ristow, D .; Scharlau, W .; Schmidl, D. & Wink, Michael ( 1994 ): Phylogenetic relationships among falcon species ( genus Falco ) according to DNA sequence variation of the cytochrome b gene.
* Wink, Michael ; Sauer-Gürth, Hedi ; Ellis, David & Kenward, Robert ( 2004 ): Phylogenetic relationships in the Hierofalco complex ( Saker -, Gyr -, Lanner -, Laggar Falcon ).
* Martínez Gómez, Juan E .; Barber, Bruian R. & Peterson, A. Townsend ( 2005 ): Phylogenetic position and generic placement of the Socorro Wren ( Thryomanes sissonii ).
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