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Phylogenetic position is disputed: their closest relatives may be the mites ( Acari ) or the Novogenuata ( the Scorpiones, Pseudoscorpiones and Solifugae ).
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Phylogenetic and position
Phylogenetic position and generic limits of Arabidopsis ( Brassicaceae ) based on sequences of nuclear ribosomal DNA: Annals of the Missouri Botanical Garden 90 ( 4 ): 603-612
Phylogenetic analyses based on 79 ribosomal proteins indicated a position of Sipuncula within Annelida.
* ( 2008 ): Phylogenetic position of the enigmatic genus Psilorhynchus ( Ostariophysi: Cypriniformes ): Evidence from the mitochondrial genome.
* Martínez Gómez, Juan E .; Barber, Bruian R. & Peterson, A. Townsend ( 2005 ): Phylogenetic position and generic placement of the Socorro Wren ( Thryomanes sissonii ).
* Martínez Gómez, Juan E .; Barber, Bruian R. & Peterson, A. Townsend ( 2005 ): Phylogenetic position and generic placement of the Socorro Wren ( Thryomanes sissonii ).
Phylogenetic and is
The phylogenetic tree is a maximum-likelihood Phylogenetic tree # Special tree types | phylogram based on samples from 266 giraffes.
Phylogenetic studies generally have shown the clouded leopard ( Neofelis nebulosa ) is basal to this group.
* Who is Who in Phylogenetic Networks research papers related to the phylogenetic network
Phylogenetic analysis shows that the devil is most closely related to quolls.
Phylogenetic analysis identified seven genotypes of yellow fever viruses, and it is assumed that they are differently adapted to humans and to the vector Aedes aegypti.
Phylogenetic classification is based solely on phylogeny.
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.
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 ).
The International Code of Phylogenetic Nomenclature, known as the PhyloCode for short, is a developing draft for a formal set of rules governing phylogenetic nomenclature.
The PhyloCode is associated with the International Society for Phylogenetic Nomenclature ( ISPN ).
hMPV is genetically similar to the avian pneumoviruses A, B and in particular type C. Phylogenetic analysis of hMPV has demonstrated the existence of two main genetic lineages termed subtype A and B containing within them the subgroups A1 / A2 and B1 / B2 respectively.
* German entomologist Willi Hennig's Phylogenetic Systematics is published in English, advancing the study of cladistics.
The Barbary Falcon is one of the rare cases that may arguably be considered a species under the Biological, but certainly not under the Phylogenetic Species Concept rather than the other way around as usual.
Phylogenetic trees based on 16S rRNA sequences have shown that the genus Actinomyces is quite diverse, exhibiting polyphyletic branching into several clusters.
Phylogenetic analysis of 26 Chordopoxviruses genomes has shown that the central region of the genome is conserved and contains ~ 90 genes.
Phylogenetic analysis suggests that this group is paraphyletic and will need division.
" The Paraphyly of Osmunda is Confirmed by Phylogenetic Analyses of Seven Plastid Loci.
Phylogenetic and their
Phylogenetic groups are given definitions based on their relationship to one another, rather than purely on physical traits such as the presence of a backbone.
Phylogenetic relationships and morphological diversity in Darwin's finches and their relatives.
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 systematics of Glassfrogs ( Amphibia: Centrolenidae ) and their sister taxon Allophryne ruthveni.
Phylogenetic and may
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 analysis of the RNA and protein sequences of poliovirus ( PV ) suggests that PV may have evolved from a C-cluster coxsackie A virus ancestor, that arose through a mutation within the capsid.
Phylogenetic analyses of D-loop DNA sequences of various lemur species suggests that the gray mouse lemur may be most closely related to the reddish-gray mouse lemur ( M. griseorufus ).
Phylogenetic and be
Phylogenetic techniques can be used as a more rigorous test.
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 analysis of the Malay population, P. curtus brongersmai, suggests a close affinity with the nominal subspecies, however, P. curtus breitensteini was determined to be as genetically distant from the original type as the species Python reticulatus.
Phylogenetic and ).
Phylogenetic relationships, ecological correlates, and molecular evolution within the Cavioidea ( Mammalia, Rodentia ).
Phylogenetic trees of species and higher taxa are used to study the evolution of traits ( e. g., anatomical or molecular characteristics ) and the distribution of organisms ( biogeography ).
( 1996 ): A Molecular Phylogenetic Survey of the Nightjars and Allies ( Caprimulgiformes ) with Special Emphasis on the Potoos ( Nyctibiidae ).
Phylogenetic relationships between Falco biarmicus and other hierofalcons ( Aves Falconidae ).
Phylogenetic relationships between Falco biarmicus and other hierofalcons ( Aves Falconidae ).
* Rice, Nathan H. ( 2005a ): Phylogenetic relationships of antpitta genera ( Passeriformes: Formicariidae ).
* Rice, Nathan H. ( 2005a ): Phylogenetic relationships of antpitta genera ( Passeriformes: Formicariidae ).
* Rice, Nathan H. ( 2005a ): Phylogenetic relationships of antpitta genera ( Passeriformes: Formicariidae ).
* Rice, Nathan H. ( 2005a ): Phylogenetic relationships of antpitta genera ( Passeriformes: Formicariidae ).
An Eocene Species of Hiodon from Montana, Its Phylogenetic Relationships, and the Evolution of the Postcranial Skeleton in the Hiodontidae ( Teleostei ).
Phylogenetic Status and Systematics of the Agamid Coryphophylax Blyth, 1861 ( Reptilia: Squamata ).
Phylogenetic relationships and historical biogeographical relationships of the genera in the family Agamidae ( Reptilia: Lacertilia ).
Phylogenetic relationships and historical biogeographical relationships of the genera in the family Agamidae ( Reptilia: Lacertilia ).
* ( 1989 ) A Phylogenetic Analysis and Taxonomy of Iguanian Lizards ( Reptilia: Squamata ).
Etheridge ( 1989 ) A Phylogenetic Analysis and Taxonomy of Iguanian Lizards ( Reptilia: Squamata ).
Phylogenetic affinities of Mabuya atlantica Schmidt, 1945, endemic to the Atlantic Ocean archipelago of Fernando de Noronha ( Brazil ): Necessity of partitioning the genus Mabuya Fitzinger, 1826 ( Scincidae: Lygosominae ) ( subscription required ).
" Mitochondrial DNA Phylogenetic Definition of a Group of ‘ Arid-Zone ’ Carduelini Finches "( PDF ).
Phylogenetic evidence supports at least three species ( a north Indian, a south Indian and a Sri Lankan species ).
* ( 2004 ): Morphology, Phylogenetic Taxonomy, and Systematics of Ichthyornis and Apatornis ( Avialae: Ornithurae ).
Plant Systematics: A Phylogenetic Approach, 2nd edition, pp. 409 – 410 ( Cistaceae ).
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