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"phylogeny" Definitions
  1. the evolutionary history of a kind of organism
  2. the evolution of a genetically related group of organisms as distinguished from the development of the individual organism
  3. the history or course of the development of something (such as a word or custom)

1000 Sentences With "phylogeny"

How to use phylogeny in a sentence? Find typical usage patterns (collocations)/phrases/context for "phylogeny" and check conjugation/comparative form for "phylogeny". Mastering all the usages of "phylogeny" from sentence examples published by news publications.

The phylogeny [the ancestral "family tree"] they report is well-supported.
Before modern gene-based phylogeny developed, that was indeed the definition of a mammal.
But indeed, it lies deep at the bottom of the fish phylogeny, from 307-million years ago... I love the depiction of it.
And his work laid the foundations for a new field of science called molecular phylogeny that has delivered astounding insights about evolutionary history.
"I had a lull in my dissertation research and decided to spend the weekends and downtime making this phylogeny," lead author Matan Shelomi said at the time.
So whatever advances have been made in supportive parenting, the process by which a gay man finds himself and his people is much the same as it ever was: Ontogeny recapitulates phylogeny.
Biologists have known about these wee beasties for well over a century, but only now can hemimastigotes be officially slotted into the evolutionary tree of life, a process more formally known as phylogeny.
If there is something of which he can be said to be truly proud, it is his scientific passion for fish—"Some Morphological Characters Considered to be Important in Gobiid Phylogeny" being a particular highlight.
Below is a simplified phylogeny showing their one phylogeny supporting gastornithiforms as anserimorphs.
The phylogeny of superrosids shown below is adapted from the Angiosperm Phylogeny Group website.
The following phylogeny of Zakerana is from Pyron & Wiens (2011). 9 species are included. Howlader, et al. (2016) gives a different phylogeny.
While the extant gymnosperms form a monophyletic group, a formal name has not been assigned to this clade. In 2018, the Gymnosperm Phylogeny Group was established, analogous to the Angiosperm Phylogeny Group and Pteridophyte Phylogeny Group, with the intention of reaching a consensus.
Archosaur phylogeny and the relationships of the Crocodylia, p. 289-332. In Benton, M.J. (ed.), The Phylogeny and Classification of Tetrapods, Vol. 1 ., Clarendon Press, Oxford.
Brittnacher, J. Evolution -- Nepenthes Phylogeny . International Carnivorous Plant Society.
The APG II system (Angiosperm Phylogeny Group II system) of plant classification is the second, now obsolete, version of a modern, mostly molecular-based, system of plant taxonomy that was published in April 2003 by the Angiosperm Phylogeny Group.Angiosperm Phylogeny Group (2003). An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II. Botanical Journal of the Linnean Society 141(4): 399-436. doi: 10.1046/j.1095-8339.2003.t01-1-00158.
This follows the work of the Angiosperm Phylogeny Group. The family Ranunculaceae sensu stricto (APG) is one of seven families included in the order Ranunculales within the eudicots according to the Angiosperm Phylogeny Group classification. The family is monophyletic with Glaucidium as sister to the remaining genera. This phylogeny is illustrated in the APG Poster.
Kluge (1991) moved the genera Sanzinia and Acrantophis into Boa, based on a phylogeny derived from morphological characters.Kluge AG. 1991. Boine Snake Phylogeny and Research Cycles. Misc. Pub. Museum of Zoology, Univ.
The full phylogeny of this genus is unknown, and research was ongoing in 2014. The following cladogram of Cucurbita phylogeny is based upon a 2002 study of mitochondrial DNA by Sanjur and colleagues.
Benton, M.J. and Clark, J.M. (1988). "Archosaur phylogeny and the relationships of the Crocodylia." Pp. 295–338 in Benton, M.J. (ed.), The phylogeny and classification of the Tetrapods, volume 1. Oxford: Clarendon Press.
The Angiosperm Phylogeny Group. 2003. "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II". Botanical Journal of the Linnean Society 141(4):399-436.
De Queiroz’s research has focused primarily on the phylogeny and evolutionary biology of squamate reptiles, including his Master’s research on the phylogeny of iguanine lizards and his Ph.D. research on the phylogeny of phrynosomatine sand lizards. He worked with his mentors Richard Estes and Richard Etheridge on the phylogeny of Squamata Estes, R., K. de Queiroz, and J. A. Gauthier. (1988) “Phylogenetic relationships within Squamata.” Pp. 119-281 in ‘’Phylogenetic Relationships of the Lizard Families’’, R. Estes and G. Pregill (eds.), Stanford Univ.
The phylogeny of Capitosauroidea according to Witzmann et al. (2016). The phylogeny of the genus Cyclotosaurus according to Witzmann et al. (2016). See also alternative phylogenies from 2017 with the description of C. naraserluki.
The following phylogeny of Rhacophorinae is from Yu et al. (2008).
The phylogeny has been obtained by Antonio Arnaiz-Villena et al.
For a phylogeny of Hemerocallidaceae, see the phylogenetic tree at Asphodelaceae.
The phylogeny has been obtained by Antonio Arnaiz-Villena et al.
The phylogeny has been obtained by Antonio Arnaiz-Villena et al.
BAli-Phy is a free software program for simultaneously estimating a multiple sequence alignment and its phylogenetic tree. BAli-Phy achieves high accuracy in alignment estimation by using information from the co-estimated phylogeny. BAli-Phy takes alignment uncertainty into account while estimating the phylogeny by averaging over possible alignments. Unlike most phylogeny inference software, input sequences need not be aligned beforehand.
Angiosperm Phylogeny Group. 2009. "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III". Botanical Journal of the Linnean Society 161(2):105-121. (see External links below).
Phylogeny and Biogeography of the Amazona ochrocephala (Aves: Psittacidae) Complex. Auk 121(2): 318-332Russello, M. A., & Amato, G. (2004). A molecular phylogeny of Amazona: implications for Neotropical parrot biogeography, taxonomy, and conservation. Molecular Phylogenetics and Evolution.
The conflicting data pertaining to phylogeny creates inconsistent marmot lineage relationship hypotheses.
Molecular analysis has clarified the group's phylogeny, as shown in the cladogram.
Extinct species assignment follows the Mikko's Phylogeny Archive, Paleofile.com website and Brodkob.
Below is a phylogeny from Schoch (2018) showing the position of Micropholis.
Colgan et al. (2006) provided further insight into the phylogeny of Caenogastropoda.
The taxonomy, phylogeny, and distributional boundary have not been fully studied yet.
Perfect phylogeny is also used in the construction of haplotype maps. By utilizing the concepts and algorithms described in perfect phylogeny one can determine information regarding missing and unavailable haplotype data. By assuming that the set of haplotypes that result from genotype mapping corresponds and adheres to the concept of perfect phylogeny (as well as other assumptions such as perfect Mendelian inheritance and the fact that there is only one mutation per SNP), one is able to infer missing haplotype data. Inferring a phylogeny from noisy VAF data under the PPM is a hard problem.
A phylogeny and classification of the South American Cichlidae (Teleostei: Perciformes). pp. 461–498 in Malabarba, L., et al. (eds.), Phylogeny and Classification of Neotropical Fishes, Porto Alegre. and Caecobarbus geertsii, the only known cavefish in Central Africa.
A phylogeny has been presented by Antonio Arnaiz-Villena et al. Origin and phylogeny has been determined by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter towards Africa and Pacific Ocean habitats.
Peter Stevens, one of the authors of all four of the APG papers, maintains a web site, the Angiosperm Phylogeny Website (APWeb), hosted by the Missouri Botanical Garden, which has been regularly updated since 2001, and is a useful source for the latest research in angiosperm phylogeny which follows the APG approach. Other sources include the Angiosperm Phylogeny Poster and The Flowering Plants Handbook.
American Journal of Botany 87 1300-08.Ferguson, C. J. and R. K. Jansen. (2002). A chloroplast DNA phylogeny of eastern Phlox (Polemoniaceae): implications of congruence and incongruence with the ITS phylogeny. American Journal of Botany 89 1324-35.
When the APG III system was published in October 2009, the Angiosperm Phylogeny Group expanded Celastraceae to include all members of the pentatomy mentioned above.Peter F. Stevens (2001 onwards). Celastrales At: Angiosperm Phylogeny Website. At: Missouri Botanical Garden Website.
The name "metallicus" is Latin meaning "the miner". The use of biochemistry and phylogeny were originally the main source of classification, but 16S rRNA sequences were performed on it to elucidate the phylogeny. Sulfolobus sp. strain 7r sp. nov.
The phylogeny based on the work of the All-Species Living Tree Project.
The phylogeny based on the work of the All-Species Living Tree Project.
The phylogeny based on the work of the All-Species Living Tree Project.
It is rare that actual data adheres to the concept of perfect phylogeny.
The phylogeny based on the work of the All-Species Living Tree Project.
The phylogeny based on the work of the All-Species Living Tree Project.
Phylogeny and classification of the Signiphoridae (Hymenoptera: Chalcidoidea). Systematic Entomology 13:465-501.
The following phylogeny of selected Rattus species is from Pagès, et al. (2010).
The phylogeny based on the work of the All-Species Living Tree Project.
The idea that ontogeny recapitulates phylogeny has been applied to some other areas.
The recent reorganization of the Glomeromycota phylogeny has renamed this species Rhizophagus aggregatum.
The cladogram is based on molecular phylogeny of six genes in Flynn, 2005.
Shultz, J.W. (1990). Evolutionary Morphology And Phylogeny of Arachnida. Cladistics 6: 1–38.
The phylogeny based on the work of the All-Species Living Tree Project.
The cladogram is based on molecular phylogeny of six genes in Flynn, 2005.
Museum Nat. History., 85.Engelmann, G. F. (1985). The phylogeny of the Xenarthra.
This group is supported by molecular phylogeny, but there are no known synapomorphies.
This group is supported by molecular phylogeny, but there are no known synapomorphies.
" Journal of computational biology 8, no. 3 (2001): 305-323. the multi-state perfect phylogeny problem using chordal graph theory,Gusfield. "The multi- state perfect phylogeny problem with missing and removable data: solutions via integer linear programming and chordal graph theory.
Modern crocodiles are considered within the group archosaurs, which also include birds, dinosaurs, and crocodilians.Benton, Michael J., and JAMES M. Clark. "Archosaur phylogeny and the relationships of the Crocodylia." The phylogeny and classification of the tetrapods 1 (1988): 295-338.
P. Burridge, 1999. Molecular phylogeny of Nemadactylus and Acantholatris (Perciformes: Cirrhitoidea), with implications for taxonomy and biogeography. Mol. Phylogenet. Evol. 13: 93–109Burridge and Smolenski (2004). Molecular phylogeny of the Cheilodactylidae and Latridae (Perciformes: Cirrhitoidea) with notes on taxonomy and biogeography.
The following phylogeny is from Pyron, et al. (2013),Pyron, R Alexander, Frank T Burbrink and John J Wiens. 2013. A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes. BMC Evolutionary Biology 2013 13:93.
In phylogenetics, bootstrapping is conducted using the columns of the character matrix. Each pseudoreplicate contains the same number of species (rows) and characters (columns) randomly sampled from the original matrix, with replacement. A phylogeny is reconstructed from each pseudoreplicate, with the same methods used to reconstruct the phylogeny from the original data. For each node on the phylogeny, the nodal support is the percentage of pseudoreplicates containing that node.
Romina Vidal-Russell is an Argentinean botanist who works in the areas of phytogeography, phylogeny, and parasitic plants, and on which she has written extensively. Her papers on the phylogeny of parasitic plants are cited on the APG website,Stevens, P.F. (2001 onwards) Angiosperm Phylogeny Website. Version 14, July 2017 (and more or less continuously updated since) www.mobot.org. Retrieved 31 July 2019 and elsewhere and her collaborations are international.
Below is the general consensus of the phylogeny of anseriforms and their stem relatives.
A supermatrix-based molecular phylogeny of the family Drosophilidae. Genetics Research 92, 25-38.
Malawimonadidae is a group of unicellular eukaryotes of outsize importance in understanding eukaryote phylogeny.
Comparative carpology of the genus Sphenostemon in the context of its taxonomy and phylogeny.
Compared to a phylogeny of an expanding virus, a phylogeny of a viral population that stays constant in size will have external branches that are shorter relative to branches on the interior of the tree. The phylogeny of HIV provides a good example of a star-like tree, as the prevalence of HIV infection rose rapidly throughout the 1980s (exponential growth). The phylogeny of hepatitis B virus instead reflects a viral population that has remained roughly consistent (constant size). Similarly, trees reconstructed from viral sequences isolated from chronically infected individuals can be used to gauge changes in viral population sizes within a host.
Molecular phylogeny analysis by Maeda et al. (2010)Maeda T., Kajita T., Maruyama T. & Hirano Y. (2010). "Molecular Phylogeny of the Sacoglossa, With a Discussion of Gain and Loss of Kleptoplasty in the Evolution of the Group". Biological Bulletin 219(1): 17-26.
This species was found to belong in a clade with Doriprismatica atromarginata in a molecular phylogeny study.Johnson R.F. & Gosliner T.M. (2012) Traditional taxonomic groupings mask evolutionary history: A molecular phylogeny and new classification of the chromodorid nudibranchs. PLoS ONE 7(4): e33479.
Phylogeny of Drosophilinae (Diptera: Drosophilidae), with comments on combined analysis and character support. Molecular Phylogenetics and Evolution 24, 249–264.van der Linde, K., Houle, D., Spicer, G. S. & Steppan, S. J. (2010). A supermatrix-based molecular phylogeny of the family Drosophilidae.
These are four of the fourteen Angiosperm Phylogeny Group. 2009. "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III". Botanical Journal of the Linnean Society 161(2):105-121. (see External links below).
In the APG III system, these three genera constitute the family Torricelliaceae.Angiosperm Phylogeny Group (2009). An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III. Botanical Journal of the Linnean Society 161(2): 105-121.
Phylogeny and new taxonomy of the Booted Eagles (Accipitriformes: Aquilinae). Zootaxa 4216 (4), 301-320.
Other options are "Do Alignment from guide tree and phylogeny" and "Produce guide tree only".
A radical solution: The phylogeny of the nudibranch family Fionidae. PLoS ONE. 11(12): e0167800.
However, the species-level phylogeny for Ambystomatidae is tentative and in need of further testing.
Baboon phylogeny In 2015 researchers found the oldest baboon fossil dating 2 million years ago.
The exact phylogeny of the family and its species continues to be discussed among bryologists.
"A molecular phylogeny and classification of Bignoniaceae". American Journal of Botany 96(9):1731-1743.
A radical solution: The phylogeny of the nudibranch family Fionidae. PLoS ONE. 11(12): e0167800.
Cytochrome b and Bayesian inference of whale phylogeny. Molecular Phylogenetics and Evolution 38, 344-354.
The Phylogeny and Classification of the Tetrapods Vol. 1.Amphibians, Reptiles, Birds. Clarendon Press, Oxford.
Peter F. Stevens. (2001 onwards). "Boraginaceae". At: Angiosperm Phylogeny Website. At: Missouri Botanical Garden Website.
A 2018 molecular phylogeny of the family Capitellidae established clear monophyly and showed 8 genera. The phylogeny utilized 36 capitellid species and combined data from 18S, 28S, H3, and COI gene sequences. This study also established Capitellidae as the sister group to Echiura. While the study attempted to map morphological characters to the molecular phylogeny, this was not phylogenetically informative and a more detailed re-evaluation of morphology could help to elucidate character trait evolution.
The family is not recognized in the APG III system of plant classification.Angiosperm Phylogeny Group. 2009. "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III". Botanical Journal of the Linnean Society 161(2):105-121.
Phylogeny based on Bass et al. 2009, Howe et al. 2011 and Bass et al. 2016.
In addition, Eotyrannus is recovered as a sister taxon of these genera in the parsimonious phylogeny.
In addition, Eotyrannus is recovered as a sister taxon of these genera in the parsimonious phylogeny.
Hansen, M. (1997). "Phylogeny and classification of the staphyliniform beetle families (Coleoptera)". Biologiske Skrifter. 48, Copenhagen.
Schrödl M. & Neusser T. P. (2010). "Towards a phylogeny and evolution of Acochlidia (Mollusca: Gastropoda: Opisthobranchia)".
Senter, P. (2004). "Phylogeny of Drepanosauridae (Reptilia: Diapsida)." Journal of Systematic Palaeontology, 2(3): 257-268.
"Systematics, phylogeny and palaeobiogeography of the ankylosaurid dinosaurs". Journal of Systematic Palaeontology: 1. doi:10.1080/14772019.2015.1059985.
Phylogeny of living Characiformes based on Betancur-Rodriguez et al. 2017: and Nelson, Grande & Wilson 2016.
Biologically, they have gained attention for their potential to shed light on the phylogeny of tapeworms.
For a more detailed discussion of the phylogeny of the cacti, see Classification of the Cactaceae.
"Molecular phylogeny of Planchonella (Sapotaceae) and eight new species from New Caledonia."Taxon (2007): 329-354.
"Molecular phylogeny of Planchonella (Sapotaceae) and eight new species from New Caledonia."Taxon (2007): 329-354.
"Molecular phylogeny of Planchonella (Sapotaceae) and eight new species from New Caledonia."Taxon (2007): 329-354.
"Molecular phylogeny of Planchonella (Sapotaceae) and eight new species from New Caledonia."Taxon (2007): 329-354.
"Molecular phylogeny of Planchonella (Sapotaceae) and eight new species from New Caledonia."Taxon (2007): 329-354.
"Molecular phylogeny of Planchonella (Sapotaceae) and eight new species from New Caledonia."Taxon (2007): 329-354.
"Molecular phylogeny of Planchonella (Sapotaceae) and eight new species from New Caledonia."Taxon (2007): 329-354.
"Molecular phylogeny of Planchonella (Sapotaceae) and eight new species from New Caledonia."Taxon (2007): 329-354.
The Angiosperm Phylogeny Website (APweb) recognizes three subfamilies, one of which is divided into two tribes.
The following phylogeny of Mus is from Barbara Lundrigan and colleagues' 2002 paper in Systematic Biology.
Ontogeny and Phylogeny is a 1977 book on evolution by Stephen Jay Gould, in which the author explores the relationship between embryonic development (ontogeny) and biological evolution (phylogeny). Unlike his many popular books of essays, it was a technical book, and over the following decades it was influential in stimulating research into heterochrony, changes in the timing of embryonic development, which had been neglected since Ernst Haeckel's theory that ontogeny recapitulates phylogeny had been largely discredited.
Phylogeny as given by Bisby et al., 2000, who put the genus into a separate family Monascaceae.
Senter, P. (2007). "A new look at the phylogeny of Coelurosauria (Dinosauria: Theropoda)." Journal of Systematic Palaeontology, ().
A detailed phylogeny to the level of order, based on the work by Novíkov & Barabaš-Krasni 2015.
Therefore, in the latest molecular phylogeny, a combined study of ecogeographic factors has been taken into account.
The cladogram presented below is based on studies compiled by Mikko Haaramo for the Mikko's Phylogeny Archive.
Peter F. Stevens. 2001 onwards. Angiosperm Phylogeny Website At: Missouri Botanical Garden Website. (see External links below).
Phylogeny and classification of the Marchantiophyta. Edinburgh Journal of Botany, vo. 66, no. 1, p. 155-198.
The following tree represents current insights in the phylogeny of the Crow family according to J. Boyd.
Savchenko, E. N. 1966. Phylogeny and systematics of the Tipulidae. Fauna Ukraini 14:63–88. In Russian.
According to molecular phylogeny, the closest relatives of the Betulaceae are the Casuarinaceae, or the she-oaks.
The following phylogeny of Dicroglossidae is from Pyron & Wiens (2011). Dicroglossidae is a sister group of Ranixalidae.
Zhao X. (1985). "Phylogeny and evolutionary stages of Dinosauria." Acta Palaeontologica Polonica 28(1-2); 295-306.
Thoughts on high systematics, phylogeny and floral morphogeny, with a note on the origin of the Angiospermae.
The phylogeny of rosids shown below is adapted from the Angiosperm Phylogeny Group website. The nitrogen-fixing clade contains a high number of actinorhizal plants (which have root nodules containing nitrogen fixing bacteria, helping the plant grow in poor soils). Not all plants in this clade are actinorhizal, however.
Perfect phylogeny is a theoretical framework that can also be used in more practical methods. One such example is that of Incomplete Directed Perfect Phylogeny. This concept involves utilizing perfect phylogenies with real, and therefore incomplete and imperfect, datasets. Such a method utilizes SINEs to determine evolutionary similarity.
The phylogeny of the teleosts has been subject to long debate, without consensus on either their phylogeny or the timing of the emergence of the major groups before the application of modern DNA-based cladistic analysis. Near et al. (2012) explored the phylogeny and divergence times of every major lineage, analysing the DNA sequences of 9 unlinked genes in 232 species. They obtained well- resolved phylogenies with strong support for the nodes (so, the pattern of branching shown is likely to be correct).
The phylogeny is based on 16S rRNA-based LTP release 132 by The All-Species Living Tree Project.
Sibley, Charles Gald & Ahlquist, Jon Edward (1990): Phylogeny and classification of birds. Yale University Press, New Haven, Conn.
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.
A recent phylogeny of the entire order Diptera places them as the sister group to all other flies.
Solza margarita is an extinct animal of uncertain phylogeny which lived about 555 mya in the Ediacaran period.
In the Pteridophyte Phylogeny Group classification of 2016 (PPG I), this species is placed in the genus Parablechnum.
In a molecular phylogeny, Syzygites megalocarpus is placed sister to Sporodinella umbellata, albeit in a clade with Rhizopus.
"Phylogeny and evolution of grammitid ferns (Grammitidaceae): a case of rampant morphological homoplasy". Taxon 53(2):415-428.
The hindwings are pale greyish brown with a faint darker line.Systematics and phylogeny of Sparganothina and related taxa.
The phylogeny is based on 16S rRNA-based LTP release 132 by 'The All-Species Living Tree' Project.
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.
"Phylogeny of Halictidae with emphasis on endemic African Halictinae" (PDF). Apidologie 39: 86–101. doi:10.1051/apido:2008002.
Below is Nancy A. Voss and Robert S. Voss's 1983 proposal for a phylogeny of the Taoniinae subfamily.
Berg, R. Y. 1958. Seed dispersal, morphology, and phylogeny of Trillium. Skr. Norske Vidensk.-Akad. Oslo, Mat.-Natkurvidensk.
This is confirmed by molecular phylogenetic research. Ciliates were never found close to animals in any molecular phylogeny.
The phylogeny of this and other closely related finches has been investigated by Antonio Arnaiz- Villena et al.
RAMSKÖLD, L. and CHEN, J.-Y. 1998. Cambrian lobopodians: morphology and phylogeny. In EDGECOMBE, G. D. (ed.) Arthropod Fossils and Phylogeny, Columbia University Press, New York, 107–150 pp. Xenusion has been reinterpreted as an Ediacaran frond animal by Tarlo, and a drawing of that interpretation has been presented by McMenamin.
Wood anatomy of Aextoxicaceae and Berberidopsidaceae is compatible with their inclusion in Berberidopsidales. Systematic Botany 28: 317–325. Angiosperm Phylogeny Group IV. 2016. An update of the angiosperm phylogeny group classification for the orders and families of flowering plants: APG IV. Botanical Journal of the Linnean Society 181: 1–20.
Phylogeny of seed plants based on all three genomic compartments: Extant gymnosperms are monophyletic and Gnetales' closest relatives are conifers. Proceedings of the National Academy of Sciences 97: 4092-4097.Soltis, Douglas E., Pamela S. Soltis and Michael J. Zanis. 2002. Phylogeny of seed plants based on evidence from eight genes .
The vampire squid (Vampyroteuthis infernalis), however, is more closely related to the octopuses than to any squid. The cladogram, not fully resolved, is based on Sanchez et al., 2018. Their molecular phylogeny used mitochondrial and nuclear DNA marker sequences; they comment that a robust phylogeny "has proven very challenging to obtain".
The phylogeny of the species separates this species and B. lesueur from lineages that emerged at a later period.
The phylogeny of extant species (excluding hybrids), according to Christenhusz et al. (2019), is shown in the following cladogram.
Bjerring, H. C. (1972). The nervus rarus in coelacanthiform phylogeny. Zoologica Scripta, 1, 57–68.Bjerring, H. C. (1993).
"A molecular genetic analysis of cuckoo phylogeny". In Payne, Robert B. The Cuckoos. Oxford University Press. pp. 90, 93. .
'The phylogeny and systematics of blind Cambrian Ptychoparioid trilobites. Palaeontology, Vol. 44, Part 1, pp. 167-207, 4 pls.
In recent years, RAPD has been used to characterize, and trace, the phylogeny of diverse plant and animal species.
"On the phylogeny and evolutionary history of pterosaurs". Pp. 139-190 in: Buffetaut, E. and Mazin, J.-M., eds.
The closest relatives of Momordica foetida can be seen in a molecular phylogeny that includes all species of Momordica.
Blackwell Scientific Publications, Oxford. and DNA sequence (molecular research) information.Oren, A., & Papke, R. T. (2010). Molecular phylogeny of microorganisms.
Stevens, P. F. (2001 onwards). Angiosperm Phylogeny Website. Version 9, June 2008 [and more or less continuously updated since].
Nectaropetalum has eight species and Pinacopodium has two. No one has yet produced a molecular phylogeny of the family.
Brower, A. V. Z. 2002. Cladistics, phylogeny, evidence and explanation - a reply to Lee. Zool. Scripta 31:221-223.
Moreover, the basal position of Manis within Pholidota suggests the group originated in Eurasia, consistent with their laurasiatherian phylogeny.
Phylogeny, Evolution, and Diversification of Caryophyllales. In: Plant Genome: Biodiversity and Evolution. Science Publishers, Inc. (USA). 1C : 187-218.
2001 onwards. Angiosperm Phylogeny Website At: Missouri Botanical Garden Website. (see External links below). Molecular synapomorphies are also known.
One 2005 phylogeny placed it as a basal member of the Feliformia, but later studies do not support this.
Another hypothesis for the phylogeny of the Entelegynae is shown below (parentheses show the genera included in the study).
Phylogeny of the cuckoo genus Coccyzus (Aves: Cuculidae): a test of monophyly. Systematics and Biodiversity. 4(4): 483-488.
The phylogeny of the Sternorrhyncha, inferred from analysis of small subunit (18S) ribosomal RNA, is shown in the cladogram.
The most recent phylogeny of caecilians is based on molecular mitogenomic evidence examined by San Mauro et al. (2014)..
Molecular phylogeny indicates that species of the genus Pyrrhula have a common ancestor with the pine grosbeak (Pinicola enucleator).
Rainer R. Schoch (2018). The putative lissamphibian stem-group: phylogeny and evolution of the dissorophoid temnospondyls. Journal of Paleontology.
When the Angiosperm Phylogeny Group published the APG II system in 2003, Themidaceae was accepted as an optional family for those who wanted to circumscribe families narrowly in the order Asparagales. When the APG III system was published in 2009, the former Themidaceae was treated as a subfamily, Brodiaeoideae, of the family Asparagaceae sensu lato. Some sources, such as ITIS, continue to use the polyphyletic groups of obsolete taxonomic systems. Other sources, such as the Angiosperm Phylogeny Website mostly follow the Angiosperm Phylogeny Group.
Andreas V. Martynov (1879–1938) recognized the close relationship between Lepidoptera and Trichoptera in his studies on phylogeny. Major contributions in the 20th century included the creation of the monotrysia and ditrysia (based on female genital structure) by Borner in 1925 and 1939. Willi Hennig (1913–1976) developed the cladistic methodology and applied it to insect phylogeny. Niels P. Kristensen, E. S. Nielsen and D. R. Davis studied the relationships among monotrysian families and Kristensen worked more generally on insect phylogeny and higher Lepidoptera too.
The APG system (Angiosperm Phylogeny Group system) of plant classification is the first version of a modern, mostly molecular-based, system of plant taxonomy. Published in 1998 by the Angiosperm Phylogeny Group, it was replaced by the improved APG II in 2003, APG III system in 2009 and APG IV system in 2016.
Cephalopods were thought to have "undoubtedly" arisen from within the tryblidiid monoplacophoran clade. However genetic studies suggest that they are more basal, forming a sister group to the Scaphopoda but otherwise basal to all other major mollusc classes. The internal phylogeny of Mollusca, however, is wide open to interpretation – see mollusc phylogeny.
C. H. Dietrich in Resh, V. H. & Carde, R. T. (Eds.) 2003 Encyclopedia of Insects. Academic Press. Of the three extant superfamilies within the Cicadomorpha, molecular phylogeny studies have placed Membracoidea as a sister group to a clade containing Cicadoidea and Cercopoidea. Within these superfamilies, not all deep phylogeny questions have been resolved.
The phylogeny of Hamamelidaceae has not been resolved with much certainty, but in one recent molecular phylogenetic study, Exbucklandia and Rhodoleia formed the most basal clade in the family.Susana Magallón. 2007. "From Fossils to Molecules: Phylogeny and the Core Eudicot Floral Groundplan in Hamamelidoideae (Hamamelidaceae, Saxifragales)". Systematic Botany 32(2):317-347.
Typotheria is a suborder of the extinct mammalian order Notoungulata and includes five families: Archaeopithecidae, Campanorcidae, Interatheriidae, Mesotheriidae, and Oldfieldthomasiidae. CifelliCifelli, Richard L. 1993. The phylogeny of the native South American ungulates. pp. 195-216 in F. S. Szalay, M. J. Novacek and M. C. McKenna (eds.) Mammal Phylogeny, Volume 2, Placentals.
Co-estimation of phylogeny and divergence times of Argonautoidea using relaxed phylogenetics. Molecular Phylogenetics and Evolution 54(3): 701–708.
This is also the nomenclature of the molecular phylogenetic based modern system of the Angiosperm Phylogeny Group (APG, 1998–2016).
Plain tiger (Danaus chrysippus) caterpillar on a milkweed (Calotropis) species in Hyderabad, India Phylogeny of the genus (without D. cleophile).
Ware was a contributor to a major study of the phylogenomics of insect evolution, and developed molecular phylogeny of hexapoda.
The species name, S. gaffneyi was named in honor of Eugene S. Gaffney, a paleontologist who specialized in turtle phylogeny.
Schiöth HB, Nordström KJ, Fredriksson R.The adhesion GPCRs; gene repertoire, phylogeny and evolution. Adv Exp Med Biol. 2010;706:1-13.
Novon 1: 53–55.Vitt, D. H. 1995. The genus Calomnion (Bryopsida): taxonomy, phylogeny, and biogeography. Bryologist 98: 338–358.
Taxon 55(3), 705-731 (pdf here) a position maintained in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
The phylogeny shown below is the one found by Worberg and co-authors. Monospecific genera are represented by species names.
Up to 2008 there were only two species Calliostoma javanicum and Calliostoma unicum that were used in molecular phylogeny studies.
Woodley, N. E. 1989. Phylogeny and classification of the “Orthorrhapous” Brachycera. Pages 1371- 1395. In J.F. McAlpine and D.M. Wood.
Leucostegia is a genus of ferns in the family Hypodematiaceae in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Category:Tephritidae genera Category:Trypetinae Aluja, Martin, and Allen L. Norrbom. Fruit Flies (Tephritidae): Phylogeny and Evolution of Behavior. CRC Press, 2000.
The species name refers to the Instituto Nacional de Biodiversidad.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
However, most recent studies using both morphological and molecular data to discuss the phylogeny and evolutionary history within the Sternorrhyncha lineage suggest that representatives of Adelgidae, Aphididae and Phylloxeridae have evolved independently and should not be combined in superfamilies. The debate is still open and more research is needed to clear the Sternorrhyncha phylogeny out.
Page is known for his work on co-speciation and in particular the development of bioinformatic software such as TreeMap, RadCon, and TreeView. Page is a co-author with Eddie Holmes of Molecular Evolution: A phylogenetic approach and editor of Tangled trees: phylogeny, cospeciation and coevolution.Page, R.D.M. ed. (2002). Tangled trees: phylogeny, cospeciation and coevolution.
This is an example of a defensive technique known as autotomy. A molecular phylogeny study of Phyllodesmium by Moore and Gosliner (2011)Moore E. J. & Gosliner T. M. (2011). "Molecular phylogeny and evolution of symbiosis in a clade of Indopacific nudibranchs". Molecular Phylogenetics and Evolution Volume 58, Issue 1, January 2011, Pages 116–123 .
According to Henn et al. 2009, phylogeny based methods take into account events that occur over long time scales and are thus less affected by stochastic fluctuations. Howell et al. 2003 suggests that selection, saturation, parallel mutations and genetic drift are responsible for the differences observed between pedigree based methods and phylogeny based methods.
The vertices of the graph can be colored by the identities of the characteristics that each attribute value comes from, so that the total number of colors equals the number of characteristics used to derive the phylogeny. Then a perfect phylogeny exists if and only if has a chordal completion that respects the coloring..
Phylogenetic studies based on molecular characters have shown that Melanoleuca does not belong to the Tricholomataceae. Moncalvo et al. presented a molecular phylogeny of the Agaricales based on LSU ribosomal RNA sequence data, including sequences of M. alboflavida and M. cognata. In this phylogeny Melanoleuca was clustered with Pluteus but with low bootstrap support.
He invented new terms, including ontogeny and phylogeny, to present his evolutionised recapitulation theory that "ontogeny recapitulated phylogeny". The two massive volumes sold poorly, and were heavy going: with his limited understanding of German, Darwin found them impossible to read. Haeckel's publisher turned down a proposal for a "strictly scholarly and objective" second edition.
The development of molecular phylogenetic methods for determining taxonomic circumscription and phylogeny led to considerable revision of angiosperm classification, and establishment of Liliales as a monophyletic group. It was clear by 1996, that the most useful system to date, that of Dahlgren, required urgent revision. The new classification was formalised with the creation of the Angiosperm Phylogeny Group (APG) system (1998–2016), based on monophyletic clades, which continued the use of Liliales as the name for the taxon. The Angiosperm Phylogeny Group APG system (1998) established a structure of monocot classification with ten orders.
At the most basic level, the presence of geographic population structure can be revealed by comparing the genetic relatedness of viral isolates to geographic relatedness. A basic question is whether geographic character labels are more clustered on a phylogeny than expected under a simple nonstructured model. This question can be answered by counting the number of geographic transitions on the phylogeny via parsimony, maximum likelihood or through Bayesian inference. If population structure exists, then there will be fewer geographic transitions on the phylogeny than expected in a panmictic model.
Ernst Haeckel supposed that embryonic development recapitulated an animal's phylogeny, and introduced heterochrony as an exception for individual organs. Modern biology agrees instead with Karl Ernst von Baer's view that development itself varies, such as by changing the timing of different processes, to cause a branching phylogeny. The concept of heterochrony was introduced by the German zoologist Ernst Haeckel in 1875, where he used it to define deviations from recapitulation theory, which held that "ontogeny recapitulates phylogeny". As Stephen Jay Gould pointed out, Haeckel's term is now used in a sense contrary to his coinage.
The phylogenetic tree, based on Papasotiropoulos 2013 and Kim 2011, with additions from Ortiz-Rivas and Martinez-Torres 2009, shows the internal phylogeny of the Aphididae. It has been suggested that the phylogeny of the aphid groups might be revealed by examining the phylogeny of their bacterial endosymbionts, especially the obligate endosymbiont Buchnera. The results depend on the assumption that the symbionts are strictly transmitted vertically through the generations. This assumption is well supported by the evidence, and several phylogenetic relationships have been suggested on the basis of endosymbiont studies.
Many other botanists echoed Lindley's earlier concerns about the phylogeny of the Liliaceae, but various schemes to divide the family gained little traction. Dahlgren (1985) suggested there were in fact forty – not one – families distributed over three orders (predominantly Liliales and Asparagales). In the context of a general review of the classification of angiosperms, the Liliaceae were subjected to more intense scrutiny. Considerable progress in plant phylogeny and phylogenetic theory enabled a phylogenetic tree to be constructed for all of the flowering plants, as elaborated by the Angiosperm Phylogeny Group (1998).
In a 2012 analysis of the phylogeny of Titanosauriformes, D'Emic (2012) considered Europasaurus to belong to Brachiosauridae, instead of being basal to the earliest brachiosaurids. The phylogeny resolved the most true brachiosaurids to date, although several potential brachiosaurids were instead determined to belong to Somphospondyli (Paluxysaurus, Sauroposeidon and Qiaowanlong). However, D'Emic was tentative in considering Europasaurus to be a confirmed brachiosaurid. While there was strong support in the phylogeny for its placement, Europasaurus, one of few basal macronarians with a skull, lacks multiple bones that display characteristic features of the group, such as caudal vertebrae.
Le Gros Clark, W. E. (1936). Evolutionary parallelism and human phylogeny. Man 36: 4–8.Le Gros Clark, W. E. (1949).
Kissel, R. (2010). "Morphology, Phylogeny, and Evolution of Diadectidae (Cotylosauria: Diadectomorpha)." Thesis (Graduate Department of Ecology & Evolutionary Biology University of Toronto).
Data from molecular phylogeny research as well as morphology supports monophyly of Holospiridae Pilsbry, 1946 and the Eucalodiidae Crosse & Fischer, 1868.
The following phylogeny of Limnonectes is from Pyron & Wiens (2011). 35 species are included. Limnonectes is a sister group of Nanorana.
Tatarinov believed in deep parallelisms in vertebrate evolution unlike the ideas of phylogeny reconstruction that make use of parsimonious character changes.
The research at CCS centers on the phylogeny and ontogeny of human semiosis, employing apes and children, respectively, as research subjects.
English: Colourful Thermophilic Archaebacteria (Heat-loving bacteria) Stain The phylogeny based on the work of the All-Species Living Tree Project.
The hindwings are pale greyish brown with thin darker brown lines toward the apex.Systematics and phylogeny of Sparganothina and related taxa.
Eckblad F-E. The genera of operculate Discomycetes. A re-evaluation of their taxonomy, phylogeny and nomenclature. Norwegian Journal of Botany.
The following phylogeny is from Pyron, et al. (2013), and includes 22 Cyrtodactylus species. Cyrtodactylus is a sister group of Hemidactylus.
He is best known for the Goldberg system, a treatise on the classification, evolution, and phylogeny of the Monocotyledon and Dicotyledons.
Leea, sometimes classified in its own family, Leeaceae, is included in Vitaceae by APG IV (2016) and the Angiosperm Phylogeny Website.
Colonial Waterbirds, 106-114.Sheldon, F. H. (1987). Phylogeny of herons estimated from DNA-DNA hybridization data. The Auk, 97-108.
Recent treatments, including the Angiosperm Phylogeny Group, have described these two groups as subfamilies within an expanded Betulaceae: Betuloideae and Coryloideae.
The species is named in honour of Dr. John W. Brown.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
Unwin, D. M., (2003). "On the phylogeny and evolutionary history of pterosaurs." Pp. 139-190. in Buffetaut, E. & Mazin, J.-M.
Ctenitis is a fern genus in the family Dryopteridaceae, subfamily Dryopteridoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Molecular analysis using mitochondrial RNA and the mitogenome has clarified the group's phylogeny within the Neuropterida, as shown in the cladogram.
In a 2006 paper on the phylogeny of extinct pleurodires, Gaffney united the two closely related genera in the tribe Cearachelyini.
The difference between the statement "B is part of A" (phylogenetic approach) and "B has evolved from A" (evolutionary approach) is, however, one of semantics rather than of phylogeny. Both express the same phylogeny, but the former emphasizes the phylogenetic continuum while the latter emphasizes a distinct shift in anatomy or ecology in B relative to A.
Cavalier-Smith has postulated that the Chlamydiae fall into the clade Planctobacteria in the larger clade Gracilicutes. However, phylogeny and shared presence of CSIs in proteins that are lineage-specific indicate that the Verrucomicrobia are the closest free-living relatives of these parasitic organisms. Comparison of ribosomal RNA genes has provided a phylogeny of known strains within Chlamydiae.
Rubia tinctorum Rubiales was an order of flowering plants in the Cronquist system, including the families Rubiaceae and Theligonaceae. The latest APG system (2009) does not recognize this order and places the families within Gentianales. Angiosperm Phylogeny Group. 2009. "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III".
"Angiosperm Phylogeny: 17 genes, 640 taxa". American Journal of Botany 98(4):704-730. The order Rosales is strongly supported as monophyletic in phylogenetic analyses of DNA sequences, such as those carried out by members of the Angiosperm Phylogeny Group.Walter S. Judd, Christopher S. Campbell, Elizabeth A. Kellogg, Peter F. Stevens, and Michael J. Donoghue. 2008.
Phytologia 27: 55–62.Eckblad F-E. (1968). The genera of operculate discomycetes. A re-evaluation of their taxonomy, phylogeny and nomenclature.
The phylogeny of varanoid lizards and the affinities of snakes. Philosophical Transactions of the Royal Society of London B 352:53-91.
Phylogeny and generic interrelationships of the Stylidiaceae (Asterales), with a possible extreme case of floral paedomorphosis. Systematic Botany, 23(3): 289-304.
Living Galliformes based on the work by John Boyd.John Boyd's website Extinct species assignment follows the Mikko's Phylogeny Archive and Paleofile.com websites.
The following phylogeny has been adapted from Blackburn, et al. (2013). Kaloula assamensis, Kaloula taprobanica, and Kaloula aureata have not been included.
Polybotrya is a genus of ferns in the family Dryopteridaceae, subfamily Polybotryoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
A radical solution: The phylogeny of the nudibranch family Fionidae. PLoS ONE. 11(12): e0167800.Korshunova, T.; Martynov, A.; Picton, B. (2017).
Walker JW (1971) Pollen Morphology, Phytogeography, and Phylogeny of the Annonaceae. Contributions from the Gray Herbarium of Harvard University, 202: 1-130.
Leptochilus is a fern genus in the family Polypodiaceae, subfamily Microsoroideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
The hindwings are white with a faint yellowish terminal line at the apex and termen.Systematics and phylogeny of Sparganothina and related taxa.
An Atlas of Fungal Ultrastructure. Longman, Green, New York. biochemical (chemotaxonomy)Ragan M.A. & Chapman D.J. (1978). A Biochemical Phylogeny of the Protists.
Lomagramma is a genus of ferns in the family Dryopteridaceae, subfamily Elaphoglossoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Pleocnemia is a genus of ferns in the family Dryopteridaceae, subfamily Elaphoglossoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Studies in molecular phylogeny suggests that the Estrildinae may have originated in India and dispersed thereafter towards Africa and Pacific Ocean habitats.
Moyle, R. G., et al. (2006). Phylogeny and evolutionary history of Old World suboscine birds (Aves: Eurylaimides). American Museum Novitates, 1-22.
Redescription of the Jeweled Gemfish, Anthias asperilinguis (Serranidae: Anthiadinae), with comments on its ontogeny, phylogeny, and ecology. Aqua 23(3): 73-95.
Cyclodium is a plant genus in the fern family Dryopteridaceae, subfamily Polybotryoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Holtz (2000) found it to be a basal coelurosaurian,Holtz, 2000. A new phylogeny of the carnivorous dinosaurs. Gaia. 15, 5-61.
Elaphoglossum is a genus of ferns in the family Dryopteridaceae, subfamily Elaphoglossoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Revision, phylogeny and comments on biogeography of soapfishes of the genus Rypticus (Teleostei: Serranidae). Bulletin of Marine Science 65(2) 337-79.
A phylogeny of living Osteichthyes, including the tetrapods, is shown in the cladogram. Whole-genome duplication took place in the ancestral Osteichthyes.
Coryphopteris is a genus of ferns in the family Thelypteridaceae, subfamily Thelypteridoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Stigmatopteris is a genus of ferns in the family Dryopteridaceae, subfamily Polybotryoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Polystichopsis is a genus of ferns in the family Dryopteridaceae, subfamily Polybotryoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Olfersia is a genus of ferns in the family Dryopteridaceae, subfamily Polybotryoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
The genus Limax sensu stricto is probably monophyletic.Klee, B. 2006 Towards a phylogeny of Limax (Gastropoda: Stylommatophora). The Malacologist. Molluscan Forum 2006.
The species name refers to Costa Rica, where the holotype was collected.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
A radical solution: The phylogeny of the nudibranch family Fionidae. PLoS ONE. 11(12): e0167800.Korshunova, T.; Martynov, A.; Picton, B. (2017).
Molecular phylogeny based on sequences of the SSU rRNA gene indicates that Remanella and Loxodes branch together into a monophyletic family Loxodidae.
Archaeothyris belongs to the Ophiacodontidae and appears in the Early Pennsylvanian The following cladogram follows the one found on Mikko's Phylogeny Archive.
Tchangmargarya originally was a subgenus of Margarya, and is elevated to a full genus based on molecular phylogeny and comparative morphology study.
Motani, R. (1997). Phylogeny of the Ichthyosauria (Amniota: Reptilia) with special reference to Triassic forms. Ph.D. dissertation, University of Toronto, Toronto, Ontario, Canada.
Gegenbaur's research program of comparative morphology incorporating ontogeny and phylogeny is still evident in the burgeoning field of evolutionary developmental biology (evo-devo).
Ward, P.S. (2007). "Phylogeny, classification, and species-level taxonomy of ants". Zootaxa 1668 549–563Bolton, B., Alpert, G., Ward, S. Naskrecki, P. (2007).
The discrepancy is thought to have arisen due to the difference between using numerous taxa versus using various genes for constructing a phylogeny.
Molecular phylogeny suggested the two genera were sister clades, but there is some evidence that the two genera may in fact be monophyletic.
The calcaneum of Fenhosuchus seems to belong to an erythrosuchid or other basal archosauriform.Parrish, J. M. (1992). Phylogeny of the Erythrosuchidae (Reptilia: Archosauriformes).
The genus Guamatela had formerly been included in the family Rosaceae before the Angiosperm Phylogeny Group placed it in the Guamatelaceae in 2009.
Genetic diversity of Maghrebian Hottentotta (Scorpiones: Buthidae) scorpions based on CO1: new insights on the genus phylogeny and distribution. African Invertebrates 52 (1).
Ceradenia is a genus of ferns in the family Polypodiaceae, subfamily Grammitidoideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Luo, Z-X, Z Kielan-Jaworowska & RL Cifelli (2002), In quest for a phylogeny of Mesozoic mammals. Acta Palaeontol. Pol. 47: 1-78.
Neocheiropteris is a genus of ferns in the family Polypodiaceae, subfamily Microsoroideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Cable bacteria are defined by their function rather than their phylogeny, and it is possible that further cable bacteria taxa will be discovered.
In the Pteridophyte Phylogeny Group classification of 2016 (PPG I), the genus Aglaomorpha is placed in the subfamily Drynarioideae of the family Polypodiaceae.
American Museum of Natural History., & . 2008. Phylogeny of extant nephilid orb-weaving spiders (Araneae, Nephilidae): testing morphological and ethological homologies. Cladistics 24: 190.
Kaiya, Zhou. "Classification and phylogeny of the Superfamily Platanistoidea, with notes on evidence of the monophyly of the Cetacea." Sci. Rep. Whale Res.
The reproductive organs have two openings. There are also differences in the wing structure.Cranston, Peter S. and Penny J Gullan. Phylogeny of Insects.
Professor Judd has been a contributor to the Angiosperm Phylogeny Group and produced his own modification of this in 1999, the Judd system.
Hertwig, S. T., 2008 - Zoologica Scripta 37(2): 141-174 Phylogeny of the Cyprinodontiformes (Teleostei, Atherinomorpha): the contribution of cranial soft tissue characters.
Phylogeny of the Zygomycota based on nuclear ribosomal sequence data. Mycologia, 98(6), 872-884. A new genus, Echinochlamydosporium, was described in 2011.
Arthromeris is a genus of ferns in the family Polypodiaceae, subfamily Drynarioideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
"Evolutionary and Biogeographic Insights on the Macaronesian Beta-Patellifolia Species (Amaranthaceae) from a Time-Scaled Molecular Phylogeny." PLoS One. 2016; 11(3): e0152456.
Monophyly and phylogeny of cuckoos (Aves, Cuculidae) inferred from osteological characters. Zoological Journal of Linnaean Society. 130(2): 263-307.Hughes JM. (2006).
A combined molecular phylogeny of Encyclia (Orchidaceae) and relationships within Laeliinae. Selbyana 24(2) 165–79. Sulpitia Raf. is a synonym of Encyclia.
Rosales is an order of flowering plants.Peter F. Stevens (2001 onwards). "Rosales". At: Trees At: Angiosperm Phylogeny Website. At: Missouri Botanical Garden Website.
"Molecular Phylogeny of the Fern Family Dryopteridaceae inferred from Chloroplast rbcL and atpB Genes". International Journal of Plant Sciences 168(9):1311-1323.
Goniophlebium is a genus of ferns in the family Polypodiaceae, subfamily Microsoroideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
However, a recent study suggests they may in fact be distinct species. The molecular phylogeny of scuticociliates is an active area of research.
"Testing the Impact of Miniaturization on Phylogeny: Paleozoic Dissorophoid Amphibians". Systematic Biology. 58 (3): 312–327. doi:10.1093/sysbio/syp029. ISSN 1063-5157. .
Ernst Haeckel supposed that embryonic development recapitulated an animal's phylogeny, and introduced heterochrony as an exception for individual organs. Modern biology agrees instead with Karl Ernst von Baer's view that development itself varies, such as by changing the timing of different processes, to cause a branching phylogeny. The herpetologist David B. Wake, in Paleobiology, wrote that the topic was "at once so obviously important and so intrinsically difficult" that few people would tackle it. The parallelism that Haeckel noted between ontogeny and phylogeny was, Wake observed, a strong argument for evolution, but hardly anyone dared to discuss it.
The breeding system has great variation across the phylogeny, and although most species are dioecious, sometimes some species may differ from this state being monoecious. Most genera in Sapindaceae are dioecious, however, most closely related to Dodonaea in the phylogeny (Diplopeltis, Diplopeltis stuartii and Cossinia) are monoecious. It has also been reported that whereas normally breeding system in Harpullia is dioecism, a few species have also been recognized as monoecious. It was stated that during evolution a general breeding-system across the phylogeny was dioecism, however, the polygamous state was intermediate or, might be partially reversible.
Press, Stanford, California. and Iguanidae,Etheridge, R., and K. de Queiroz. (1988) “A phylogeny of Iguanidae.” Pp. 283-367 in “Phylogenetic Relationships of the Lizard Families”, R. Estes and G. Pregill (eds.), Stanford Univ. Press, Stanford, California. respectively, and with Jacques Gauthier on the phylogeny of Lepidosauromorpha.Gauthier, J. A., R. Estes, and K. de Queiroz. (1988) “A phylogenetic analysis of Lepidosauromorpha.” Pp. 15-98 in “Phylogenetic Relationships of the Lizard Families,” R. Estes and G. Pregill (eds.), Stanford Univ. Press, Stanford, California. He conducted research, including several publications with Jonathan Losos, on the phylogeny and adaptive radiation of Anolis lizards.
While the actual phylogeny of the modern amphibians is not well understood, their ancestors are descended from one line of batrachomorphs.Laurin, M. (1996): Phylogeny of Stegocephalians, from the Tree of Life Web Project All other living tetrapods (reptiles, birds and mammals) are descended from one branch of reptiliomorphs, the amniotes. Amniotes achieved dominance, while all other reptiliomorphs and most batrachomorphs have gone extinct.
However, some phylogenetic studies have recovered them as closer to gamefowl (Galliformes). Below is the general consensus of the phylogeny under the hypothesis that they are members of Anserimorphae. A 2017 paper concerning the evolution and phylogeny of the giant fowl by Worthy and colleagues have found phylogenetic support in finding the mihirungs to be the sister taxon to Gastornithidae. Worthy et al.
The phylogeny of Malpighiales is, at its deepest level, an unresolved polytomy of 16 clades. It has been estimated that complete resolution of the phylogeny will require at least 25000 base pairs of DNA sequence data per taxon. A similar situation exists with Lamiales and it has been analyzed in some detail. The phylogenetic tree shown below is from Wurdack and Davis (2009).
The phylogeny, geologic history, and classification of the Crinoidea was discussed by Wright et al. (2017). These authors presented new phylogeny-based and rank- based classifications based on results of recent phylogenetic analyses. Their rank-based classification of crinoid higher taxa (down to Order), not fully resolved and with numerous groups incertae sedis (of uncertain placement), is illustrated in the cladogram.
Liliales is an order of monocotyledonous flowering plants in the Angiosperm Phylogeny Group and Angiosperm Phylogeny Web system, within the lilioid monocots. This order of necessity includes the family Liliaceae. The APG III system (2009) places this order in the monocot clade. In APG III, the family Luzuriagaceae is combined with the family Alstroemeriaceae and the family Petermanniaceae is recognized.
Phylogeny within the genus Phrynocephalus is not well understood yet. There is a lack of data and controversy between opinions regarding both phylogenetic relationships and species vs. subspecies status of the different forms Phrynocephalus helioscopus and Phrynocephalus persicus, also called the "helioscopus-persicus complex". There is an ongoing scientific debate about the phylogeny and the taxonomic format of Phrynocephalus persicus.
Fungal Diversity is an international journal which publishes papers spanning all facets of the field of mycology. It is a peer-reviewed scientific journal that covers the biodiversity, and systematic and molecular phylogeny of the fungi, including lichens. The coverage encompasses biodiversity, and systematic and molecular phylogeny. The content includes novel research articles and review articles, all of which are peer reviewed.
As with all statistical analysis, the estimation of phylogenies from character data requires an evaluation of confidence. A number of methods exist to test the amount of support for a phylogenetic tree, either by evaluating the support for each sub-tree in the phylogeny (nodal support) or evaluating whether the phylogeny is significantly different from other possible trees (alternative tree hypothesis tests).
Skulls of Eurhinosaurus and the related Temnodontosaurus The cladogram below is based on Sander (2000)Sander,P.M.(2000). "Ichthyosauria: their diversity, distribution, and phylogeny", Paläontologische Zeitschrift 74: 1–35, Maisch and Matzke (2000), Maisch (2010)Maisch M. 2010. Phylogeny, Systematics, and Origin of The Ichthyosauria-The State of the Art. Palaeodiversity. 3: 151-214 and an analysis by Marek et al (2015).
A major cladistic study of land plants was published in 1997 by Kenrick and Crane; this both established the concept of the polysporangiophytes and presented a view of their phylogeny. Since 1997 there have been continual advances in understanding plant evolution, using RNA and DNA genome sequences and chemical analyses of fossils (e.g., Taylor et al. 2006), resulting in revisions to this phylogeny.
Rogozin et al. in 2009 noted that "The deep phylogeny of eukaryotes is an extremely difficult and controversial problem." , there appears to be a consensus that the six supergroup model proposed in 2005 does not reflect the true phylogeny of the eukaryotes and hence how they should be classified, although there is no agreement as to the model which should replace it.
"Phylogeny of the radula-less dorids (Mollusca, Nudibranchia), with the description of a new genus and a new family". Zoologica Scripta 28: 315-360. .
Vinogradov S. N., Hoogewijs D.,Arredondo-Peter R., What are the origins and phylogeny of plant hemoglobins?, Commun. Integrat. Biol., 4 (2011) 443-445.
A tale that morphology fails to tell: A molecular phylogeny of Aeolidiidae (Aeolidida, Nudibranchia, Gastropoda). PLoS ONE 8(5): e63000. doi:10.1371/journal.pone.0063000.
The phylogeny is based on 16S rRNA- based LTP release 123 by 'The All-Species Living Tree' Project.'The All- Species Living Tree' Project.
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.'The All-Species Living Tree' Project.
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.'The All-Species Living Tree' Project.
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.'The All-Species Living Tree' Project.
Phylogeny based on Bass et al. 2009, Howe etal. 2011 and Silar 2016. In 2019, Cercozoa were recognized as sister to Retaria in Rhizaria.
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.'The All-Species Living Tree' Project.
However, there has not been a consensus with regard to the phylogeny of P. carnifex so no one phylogenetic tree can be termed correct.
Grande C., Templado J., Cervera J. L. & Zardoya R. (2004). "Molecular Phylogeny of Euthyneura (Mollusca: Gastropoda)". Molecular Biology and Evolution 21(2): 303-313. .
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.'The All-Species Living Tree' Project.
Wilson, Mark VH, and Tiiu Märss. "Thelodont phylogeny revisited, with inclusion of key scale-based taxa." Estonian Journal of Earth Sciences 58.4 (2009): 297œ310.
Schwenk, K. 1994. Why snakes have forked tongues. Science 263:1573-1577Cooper, W. E. 1995b. Foraging mode, prey chemical discrimination, and phylogeny in lizards.
Its isolation in the phylogeny of the tribe suggests it is a relict taxon, one of many relict plants that grow in the Caucasus.
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.'The All-Species Living Tree' Project.
Sparganothina anopla is a species of moth of the family Tortricidae. It is found in Veracruz, Mexico.Systematics and phylogeny of Sparganothina and related taxa.
Sparganothina cristata is a species of moth of the family Tortricidae. It is found in Veracruz, Mexico.Systematics and phylogeny of Sparganothina and related taxa.
Sparganothina veracruzana is a species of moth of the family Tortricidae. It is found in Veracruz, Mexico.Systematics and phylogeny of Sparganothina and related taxa.
Sparganothina nana is a species of moth of the family Tortricidae. It is found in Costa Rica.Systematics and phylogeny of Sparganothina and related taxa.
Sparganothina volcanica is a species of moth of the family Tortricidae. It is found in Costa Rica.Systematics and phylogeny of Sparganothina and related taxa.
Sparganothina trispinosa is a species of moth of the family Tortricidae. It is found in Costa Rica.Systematics and phylogeny of Sparganothina and related taxa.
Sparganothina pollicis is a species of moth of the family Tortricidae. It is found in Costa Rica.Systematics and phylogeny of Sparganothina and related taxa.
Fossil Hepialoidea appear to be few.Kristensen, N. P. and Skalski, A.W. (1999). Phylogeny and paleontology. Pages 7-25 in: Lepidoptera: Moths and Butterflies. 1.
Redefining the damselfly families: a comprehensive molecular phylogeny of Zygoptera (Odonata). Systematic Entomology, 39(1), 68-96. The family is divided into several subfamilies.
The problematic phylogeny sampling of early studies has been demonstrated by subsequent studies that have found the Q-M378 descendant branch in South Asia.
The following is a partial phylogeny of Rhacophorus from Pyron & Wiens (2011). Only nine species are included. Rhacophorus is a sister group of Polypedates.
Bello & Grimaldi de Zio (1998), Phylogeny of the genera of the Stygarctidae and related families (Tardigrada: Heterotardigrada). Zoologischer Anzeiger, vol. 237, p. 171-183.
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.'The All-Species Living Tree' Project.
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.'The All-Species Living Tree' Project.
Yamane, Seiki. Morphological and Taxonomic Studies on Vespinae Larvae, With Reference to the Phylogeny of the Subfamily Vespinae (Hymenoptera: Vespidae). Insecta Matsumarana. Series Entomology.
"On the phylogeny and evolutionary history of pterosaurs". Pp. 139-190 in: Buffetaut, E. and Mazin, J.-M., eds. Evolution and Palaeobiology of Pterosaurs.
A molecular phylogeny study in 2007 also supported this old idea, while its conclusions about other phyla agreed with those of several other analyses.
"Molecular phylogeny of the helicoid land snails (Pulmonata: Stylommatophora: Helicoidea), with special emphasis on the Camaenidae". Journal of Molluscan Studies 73(4): 411-415. .
Sorenson, Michael D.; Payne, Robert B. (2005). "A molecular genetic analysis of cuckoo phylogeny". In Payne, Robert B. The Cuckoos. Oxford University Press. pp.
Phylogeny of subtribe Pyrinae (formerly the Maloideae, Rosaceae): Limited resolution of a complex evolutionary history. Plant Systematics and Evolution. 266(1–2): 119–145.
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.'The All-Species Living Tree' Project.
In 2019, Howard Rachlin and colleagues proposed group selection of behavioural patterns, such as learned altruism, during ontogeny parallel to group selection during phylogeny.
The phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project.'The All-Species Living Tree' Project.
"Molecular systematics of social skinks: phylogeny and taxonomy of the Egernia group (Reptilia: Scincidae)". Zool. J. Linn. Soc. 154 (4): 781-794. (HTML abstract).
Tykoski, R. S. 2005. Anatomy, ontogeny, and phylogeny of coelophysoid theropods. Unpublished PhD thesis, University of Texas at Austin, 552 pp.Kammerer, C. F. 2010.
Response to Comment by Faurby, Werdelin and Svenning. Genome biology, 17(1), 1. Below is the current understanding of the phylogeny of acinonychin genera.
Psen monticola is a species of aphid wasp in the family Crabronidae. It is found in North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Protoalligator is an extinct genus of crocodilian which lived during the Paleocene. It is considered to be an alligatoroid, but its exact phylogeny is uncertain.
Triepeolus rufithorax is a species of cuckoo bee in the family Apidae. It is found in North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Neopasites fulviventris is a species of cuckoo bee in the family Apidae. It is found in North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Gorytes willcoxi is a species of sand wasp in the family Crabronidae. It is found in North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Anthophora fedorica is a species of anthophorine bee in the family Apidae. It is found in North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Conanthalictus bakeri is a species of sweat bee in the family Halictidae. It is found in North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012. Cladistics 28(1): 80-112.
The currently accepted phylogeny is based on 16S rRNA-based LTP release 123 by The All-Species Living Tree Project All-Species Living Tree Project.
Saccharomyces paradoxus worldwide distribution. Populations are represented in different colours. Green asterisks indicate recent introductions of the European type. Phylogeny of main Saccharomyces paradoxus populations.
Shen, C. Fu, & P. Borsa. 2012. Genus-level taxonomic changes implied b mitochondrial phylogeny of grey mullets (Teleostei: Mugilidae). Comptes Rendus Biologies, 335: 687-697.
Shen, C. Fu, & P. Borsa. 2012. Genus-level taxonomic changes implied b mitochondrial phylogeny of grey mullets (Teleostei: Mugilidae). Comptes Rendus Biologies, 335: 687-697.
Lepidobotryaceae is a flowering plant family in the order Celastrales."Lepidobotryaceae" In: Peter F. Stevens (2001 onwards). Angiosperm Phylogeny Website. In: Missouri Botanical Garden Website.
Lastreopsis, known as shieldfern, is a genus of ferns in the family Dryopteridaceae, subfamily Elaphoglossoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
Hallas, JM and Gosliner, TM. (2015) Family Matters: the first molecular phylogeny of the Onchidorididae (Mollusca, Gastropoda, Nudibranchia). Molecular Phylogenetics and Evolution, 88: 16-27.
Wenying Zhuang (July 27, 1948) is a Chinese mycologist. She is known for her contributions to the study of species diversity and phylogeny of Ascomycetes.
DNA analysesRan, J.-H., Wei, X.-X. & Wang, X.-Q. 2006. Molecular phylogeny and biogeography of Picea (Pinaceae): Implications for phylogeographical studies using cytoplasmic haplotypes.
Sparks, J.S. (2004): Molecular phylogeny and biogeography of the Malagasy and South Asian cichlids (Teleostei: Perciformes: Cichlidae). Molecular Phylogenetics and Evolution, 30 (3): 599–614.
A molecular phylogeny of the genus Alloteropsis (Panicoideae, Poaceae) suggests an evolutionary reversion from C4 to C3 photosynthesis. Annals of Botany 103(1): 127–136. .
Witt, T. J. & Ronkay, L. (2011). "Lymantriinae and Arctiinae - Including Phylogeny and Check List of the Quadrifid Noctuoidea of Europe". Noctuidae Europaeae. 13: 1-448.
"The phylogenetic utility of chloroplast and nuclear DNA markers and the phylogeny of the Rubiaceae tribe Spermacoceae". Molecular Phylogenetics and Evolution 49(3):843-866.
Schorer (2016:293)Schorer, Nicolas. 2016. The Dura Language: Grammar and Phylogeny. Leiden: Brill. classifies Dura as part of his newly proposed Greater Magaric branch.
Sparganothina beckeri is a species of moth of the family Tortricidae. It is found in São Paulo, Brazil.Systematics and phylogeny of Sparganothina and related taxa.
Sparganothina lutea is a species of moth of the family Tortricidae. It is found in Pichincha Province, Ecuador.Systematics and phylogeny of Sparganothina and related taxa.
Sparganothina tena is a species of moth of the family Tortricidae. It is found in Napo Province, Ecuador.Systematics and phylogeny of Sparganothina and related taxa.
Wilson, Jeffrey A., and Paul C. Sereno. "Early Evolution and Higher-Level Phylogeny of Sauropod Dinosaurs." Journal of Vertebrate Paleontology 18.Sup002 (1998): 1-79.
The following phylogeny of the genus Microhyla is from Khatiwada, et al. (2017). 27 species are listed, including various newly described species from South Asia.
The CapsalidaeBychowsky, B.E. (1957) Monogenetic Trematodes. Their systematic and phylogeny. Akad. Nauka. USSR. English translation by the American Institute of Biological Science, Washington. 509 pp.
Shen, C. Fu, & P. Borsa. 2012. Genus-level taxonomic changes implied b mitochondrial phylogeny of grey mullets (Teleostei: Mugilidae). Comptes Rendus Biologies, 335: 687-697.
Huerteales is the botanical name for an order of flowering plants.Peter F. Stevens (2001 onwards). "Huerteales". In: Angiosperm Phylogeny Website. In: Missouri Botanical Garden Website.
The alternative taken in the Pteridophyte Phylogeny Group classification of 2016 (PPG I) is to split Blechnum into a number of smaller genera, including Doodia.
The term "phylogeny" derives from the German Phylogenie, introduced by Haeckel in 1866, and the Darwinian approach to classification became known as the "phyletic" approach.
The ringed kingfisher is related to the belted kingfisher.Moyle, R.G. (2006). "A molecular phylogeny of kingfishers (Alcedinidae) with insights into early biogeographic history". Auk no.
Molecular phylogeny of owls (Strigiformes) inferred from DNA sequences of the mitochondrial cytochrome b and the nuclear RAG-1 gene. Ardea 97(4):581-591.
These names are not very indicative, as past theories of development were very confusing.Gould, S.J. 1977. Ontogeny and phylogeny. Belknap Press of Harvard University Press.
Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012. Cladistics 28(1): 80-112.
The species name refers to La Selva Biological Station were the type specimen was collected.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
The head is covered with enlarged shields.Kluge AG (1993). "Calabaria and the phylogeny of erycine snakes". Zoological Journal of the Linnean Society 107: 293-351.
Schrödl M. & Neusser T. P. (2010). "Towards a phylogeny and evolution of Acochlidia (Mollusca: Gastropoda: Opisthobranchia)". Zoological Journal of the Linnean Society 158: 124-154. .
15: t. 1289. 1829. Bendiksby, M., Thorbek, L., Scheen, A.-C., Lindqvist, C. & Ryding, O. (2011). An updated phylogeny and classification of Lamiaceae subfamily Lamioideae.
Under this phylogeny, most traditional aetosaurines are more closely related to Desmatosuchus than they are to Aetosaurus, and the clade Aetosaurinae can only include Aetosaurus.
Trans Zool Soc Lond 34:263–345Mayr G (2011) The phylogeny of charadriiform birds (shorebirds and allies)––reassessing the conflict between morphology and molecules. Zool J Linn Soc 161:916–934 however this is also considered convergent evolution. DNA-DNA hybridisation as well as RAG-1 and myoglobin intron-II sequence data supports a link to Recurvirostridae.Sibley CG & Ahlquist JE (1990) Phylogeny and classification of birds.
Angiosperm phylogeny of orders based on classification by the Angiosperm Phylogeny Group. The figure shows the number of inferred independent origins of C3-C4 photosynthesis and C4 photosynthesis in parentheses. Phylogenetic reconstruction and ancestral state reconstruction proceed by assuming that evolution has occurred without convergence. Convergent patterns may, however, appear at higher levels in a phylogenetic reconstruction, and are sometimes explicitly sought by investigators.
Characiformes is an order of ray-finned fish, comprising the characins and their allies. Grouped in 18 recognized families, more than 2000 different species are described, including the well-known piranha and tetras.; Buckup P.A.: "Relationships of the Characidiinae and phylogeny of characiform fishes (Teleostei: Ostariophysi)", Phylogeny and Classification of Neotropical Fishes, L.R. Malabarba, R.E. Reis, R.P. Vari, Z.M. Lucena, eds. (Porto Alegre: Edipucr) 1998:123-144.
Cadlinidae is a family of sea slugs, dorid nudibranchs, marine gastropod mollusks in the superfamily Doridoidea. Molecular phylogenetic studies and their taxon-sampling schemes can have a strong influence of the resulting phylogeny. Research by R.F. Johnson in 2011Johnson R. F. (2011) "Breaking family ties: taxon sampling and molecular phylogeny of chromodorid nudibranchs (Mollusca, Gastropoda)". Zoologica Scripta 40(2): 137-157. DOI:10.1111/j.1463-6409.2010.00457.x.
Krause in 2010 during his lecture on laughter at the 11th Symposium of the Cologne-Bonn Academy for Psychotherapy in Bonn and the Annual Meeting of the German professional society for psychodynamic psychotherapy: Laughter in the therapeutic context - regarding the phylogeny and ontogeny of laughter - implications for therapeutic work. Means: Laughing in the therapeutic context - to phylogeny and ontogeny of laughter - implications for therapeutic work (in German).
Although the authors did not reconstruct a phylogeny from their simulated results, the dynamics they found were consistent with a ladder-like viral phylogeny exhibiting low strain diversity and rapid lineage turnover. Later work by Ferguson and colleagues adopted an agent-based approach to better identify the immunological and ecological determinants of influenza evolution. The authors modeled influenza's hemagglutinin as four epitopes, each consisting of three amino acids. They showed that under strain-specific immunity alone (with partial cross-immunity between strains based on their amino acid similarity), the phylogeny of influenza A/H3N2's HA was expected to exhibit 'explosive genetic diversity', a pattern that is inconsistent with empirical data.
Palaeopleurosaurus is an extinct genus of diapsid reptiles belonging to the group Sphenodontia.Dupret, V. (2004). The pleurosaurs: anatomy and phylogeny. Revue de Paléobiologie, 9: 61-80.
Neopasites is a genus of cuckoo bees in the family Apidae. There are about 5 described species in Neopasites.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
A Molecular Phylogeny for Yponomeutoidea (Insecta, Lepidoptera, Ditrysia) and Its Implications for Classification, Biogeography and the Evolution of Host Plant Use. PLoS One. 8(1): e55066.
Conanthalictus is a genus of sweat bees in the family Halictidae. There are about 13 described species in Conanthalictus.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Taxonus is a genus of common sawflies in the family Tenthredinidae. There are about 8 described species in Taxonus.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Burridge and Smolenski (2004). Molecular phylogeny of the Cheilodactylidae and Latridae (Perciformes: Cirrhitoidea) with notes on taxonomy and biogeography. Molecular Phylogenetics and Evolution 30: 118–127.
The Phylogeny of the Genus Clostridium: Proposal of Five New Genera and Eleven New Species Combinations. International Journal of Systematic Bacteriology. October 1994 vol. 44 no.
"Evolutionary and Biogeographic Insights on the Macaronesian Beta- Patellifolia Species (Amaranthaceae) from a Time-Scaled Molecular Phylogeny." PLoS One. 2016; 11(3): e0152456. Schrader, H.A. (1822).
Johnson R.F. & Gosliner T.M. (2012) Traditional taxonomic groupings mask evolutionary history: A molecular phylogeny and new classification of the chromodorid nudibranchs. PLoS ONE 7(4): e33479.
The currently accepted phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project 'The All-Species Living Tree' Project.
Johnson R.F. & Gosliner T.M. (2012) Traditional taxonomic groupings mask evolutionary history: A molecular phylogeny and new classification of the chromodorid nudibranchs. PLoS ONE 7(4): e33479.
Johnson R.F. & Gosliner T.M. (2012) Traditional taxonomic groupings mask evolutionary history: A molecular phylogeny and new classification of the chromodorid nudibranchs. PLoS ONE 7(4): e33479.
Johnson R.F. & Gosliner T.M. (2012) Traditional taxonomic groupings mask evolutionary history: A molecular phylogeny and new classification of the chromodorid nudibranchs. PLoS ONE 7(4): e33479.
The order includes only one other family, the Winteraceae.Peter F. Stevens (2001 onwards). "Canellaceae" At: Angiosperm Phylogeny Website. At: Botanical Databases At: Missouri Botanical Garden Website.
Fritsch, P. W., Morton, C. M., Chen, T., & Meldrum, C. (2001). Phylogeny and Biogeography of the Styracaceae. Int. J. Plant Sci. 162 (6 Suppl.): S95–S116.
A recent phylogeny based on the work Betancur-Rodriguez et al. 2017. The Gibberichthyidae (gibberfishes) and Hispidoberycidae (spiny-scale pricklefish) of suborder Stephanoberycoidei were not examined.
The species name refers to the spined sacculus and is derived from Latin spinula (meaning a small spine).Systematics and phylogeny of Sparganothina and related taxa.
The species name refers to the high altitude collecting site and is derived from Latin alta (meaning high).Systematics and phylogeny of Sparganothina and related taxa.
1\. Kong, H.-Z., Chen, Z.-D. & Lu, A.-M. (2002) Phylogeny of Chloranthus (Chloranthaceae) based on nuclear ribosomal ITS and plastid TRNL-F sequence data.
Danforth, B. N. (1999). "Phylogeny of the bee genus Lasioglossum (Hymenoptera: Halictidae) based on mitochondrial COI sequence data" (PDF). Systematic Entomology 24, 377-393. Retrieved from .
The genus is named for Dr. Thierry Deuve (MNHN).The Epicopeiidae: phylogeny and a redefinition, with the description of new taxa (Lepidoptera: Drepanoidea) Joël Minet, 2002.
The currently accepted phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project 'The All-Species Living Tree' Project.
The currently accepted phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project 'The All-Species Living Tree' Project.
Jörger et al. (2010) moved Sacoglossa into the Panpulmonata. A molecular phylogeny analysis by Maeda et al. (2010) confirmed the placement of Cylindrobulla within the Sacoglossa.
Carmona et al.Carmona, L., Pola, M., Gosliner, T.M. & Cervera, J.L. (2013). A tale that morphology fails to tell: a molecular phylogeny of Aeolidiidae (Aeolidida, Nudibranchia, Gastropoda).
The currently accepted phylogeny is based on 16S rRNA-based LTP release 123 by 'The All-Species Living Tree' Project 'The All-Species Living Tree' Project.
The currently accepted phylogeny is based on 16S rRNA-based LTP release 123 by The All-Species Living Tree Project 'The All-Species Living Tree' Project.
Medusandra is a genus of flowering plants in the family Peridiscaceae."Peridiscaceae" At: Peter F. Stevens (2001 onwards). Angiosperm Phylogeny Website. At: Missouri Botanical Garden Website.
Sparganothina covelli is a species of moth of the family Tortricidae. It is found in Bolivia.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
Sparganothina venezolana is a species of moth of the family Tortricidae. It is found in Venezuela.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
Psen is a genus of aphid wasps in the family Crabronidae. There are at least 90 described species in Psen.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Townsendiellini is a tribe of bees in the family Apidae. There are at least 3 described species in Townsendiellini. Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Habropoda is a genus of anthophorine bees in the family Apidae. There are at least 50 described species in Habropoda.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Tromatobia is a genus of ichneumon wasps in the family Ichneumonidae. There are at least 4 described species in Tromatobia.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Dufourea is a genus of sweat bees in the family Halictidae. There are at least 160 described species in Dufourea.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Stelis perpulchra is a species of insect in the family Megachilidae. It is found in Central America and North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Origin and phylogeny has been obtained by Antonio Arnaiz- Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
A new carnivorous cynodont from the Ischigualasto Formation (Late Triassic, Argentina), with comments on eucynodont phylogeny. Journal of Vertebrate Paleontology 16:271–84.Romer, A. S. (1969).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al.. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz- Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
The phylogeny of the genus remains unknown, but morphologically A. racemosa appears to most closely resemble A. traversii, the only other New Zealand species in the genus.
Johnson R. F & Gosliner T. M. (2012). "Traditional taxonomic groupings mask evolutionary history: A molecular phylogeny and new classification of the chromodorid nudibranchs". PLoS One 7: e33479.
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al.. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
The phylogeny of the genus remains unknown, but morphologically A. traversii appears to most closely resemble A. racemosa, the only other New Zealand species in the genus.
Monogenetic Trematodes their systematics and phylogeny. English translation edited by W. J. Hargis Jr. Washington: American Institute of Biological Sciences Archive.org.Hayward, C. (2005). Monogenea Polyopisthocotylea (ectoparasitic flukes).
This means that the decoding mechanisms used by the central nervous system to interpret such movements and produce adequate motor output probably also vary depending on phylogeny.
1.J.C.T. Gonzalez, B.C. Sheldon, N.J. Collar, J.A. Tobias. 2013.A comprehensive molecular phylogeny for the hornbills (Aves:Bucerotidae). Molecular Phylogenetics and Evolution. 67(2): 468-483 2.
"Pterosaur phylogeny and comments on the evolutionary history of the group". Pp. 105-137 in: Buffetaut, E. and Mazin, J.-M., eds. Evolution and Palaeobiology of Pterosaurs.
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
"Toward a resolution of Campanulid phylogeny, with special reference to the placement of Dipsacales". Taxon 57(1):53-65. The inclusion of Pseudobotrys in Cardiopteridaceae remains doubtful.
The two genera were formerly classified in the family Loganiaceae.Peter F. Stevens (2001 onwards). "Gelsemiaceae" At: Angiosperm Phylogeny Website. At: Botanical Databases At: Missouri Botanical Garden Website.
From one of their data matrices, they derived a well supported phylogeny for the order, as well as strongly supported relationships among the four orders of malvids.
"Evolutionary and Biogeographic Insights on the Macaronesian Beta-Patellifolia Species (Amaranthaceae) from a Time-Scaled Molecular Phylogeny." PLoS One. 2016; 11(3): e0152456. Ulbrich, O.E. (1934). "Chenopodiaceae".
The following phylogeny is from Systematics, Evolution and Biogeography of the Compositae, except the tribe Gundelieae is recognized and the genus Trichospira is now included in Vernonieae.
A.R. Palmer and L.N. Repina (1993). Through a Glass Darkly: Taxonomy, Phylogeny and Biostratigraphy of the Olenellina. The University of Kansas Paleontological Contributions 3, pp. 1-35.
Asphodeline tenuior, the thin asphodeline, is a species of plant in the family Asphodelaceae, subfamily Asphodeloideae.Stevens, P.F. (2001 onwards). "Asphodeloideae". Angiosperm Phylogeny Website. Retrieved 2016-06-10.
It is clear that the phylogeny of Orrorin is uncertain, however the evidence of the evolution of bipedalism is an invaluable discovery from this early fossil hominin.
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz- Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
The complete mitochondrial genome (18,012 base pairs in length) of Quasipaa spinosa has been sequenced, helping to shed light into the phylogeny of Quasipaa and related frogs.
Passerea was not recovered in other studies.Prum, R.O. et al. (2015) A comprehensive phylogeny of birds (Aves) using targeted next- generation DNA sequencing. Nature 526, 569–573.
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Coelostathma cocoana is a species of moth of the family Tortricidae. It is found in Costa Rica.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
Coelostathma continua is a species of moth of the family Tortricidae. It is found in Costa Rica.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
Coelostathma pygmaea is a species of moth of the family Tortricidae. It is found in Costa Rica.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
Coelostathma xocoatlana is a species of moth of the family Tortricidae. It is found in Costa Rica.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
Among these, it belonged to the Hesperornithidae, along with Hesperornis, the well-known namesake genus.Mortimer, M. (2004). The Theropod Database: Phylogeny of taxa . Retrieved 2013-MAR-02.
The leaf consists of a single leaflet on the end of a rachis.Glossary In: Peter F. Stevens (2001 onwards). Angiosperm Phylogeny Website. In: Missouri Botanical Garden Website.
Classification is the grouping of organisms into progressively more inclusive groups based on phylogeny and phenotype, while nomenclature is the application of formal rules for naming organisms.
Tykoski, R. S. 1998. The osteology of Syntarsus kayentakatae and its implications for ceratosaurid phylogeny. Master's thesis, The University of Texas at Austin, Austin, Texas, 217 pp.
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al.. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al.. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al.. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al.. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al.. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al.. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al.. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz- Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats).
The phylogeny of basal metasuchians has experienced many revisions in recent years. The phylogeny of notosuchians has been particularly revised, with the construction of Sebecia by Larsson and Sues (2007) to include peirosaurids in the clade. Previously, peirosaurids were placed outside Notosuchia. Larsson and Sues (2007) also suggested that Sebecosuchia (containing the families Baurusuchidae and Sebecidae) was polyphyletic, as Baurusuchus was placed outside Sebecia, which itself was placed outside Notosuchia.
Mickelia is a genus of ferns in the family Dryopteridaceae, subfamily Elaphoglossoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). It is one of the six genera of bolbitidoid ferns and is sister to the very large genus Elaphoglossum.Robbin C. Moran, Paulo H. Labiak, and Michael Sundue. 2010. "Phylogeny and character evolution of the bolbitidoid ferns (Dryopteridaceae)". International Journal of Plant Sciences 171(5):547-559.
The past three decades have seen a dramatic increase in the use of DNA sequences for reconstructing phylogeny and a parallel shift in emphasis from evolutionary taxonomy towards Hennig's 'phylogenetic systematics'. Today, with the advent of modern genomics, scientists in every branch of biology make use of molecular phylogeny to guide their research. One common method is multiple sequence alignment. Cavalier-Smith, G. G. Simpson and Ernst MayrMahner, Martin; Bunge, Mario.
The species was first described, then named as Cuthona herrerai in 2002. It was a Cuthona species until a DNA phylogeny of the former family Tergipedidae resulted in most species of Cuthona being transferred to the genus Tenellia, including Cuthona herrerai which became Tenellia herrerai.Cella, K; Carmona Barnosi, L.; Ekimova, I; Chichvarkhin, A; Schepetov, D; Gosliner, T. M. (2016). A radical solution: The phylogeny of the nudibranch family Fionidae.
Buffetaut E. 1982. Radiation évolutive, paléoécologie et biogéographie des crocodiliens mésosuchiens. Mémoires de la Sociéte Géologique de France 42:1–88. However, phylogenetic analyses from the 1980s, 1990s and early 2000s found Pelagosaurus to be the sister taxon to both Teleosauridae and Metriorhynchidae.Benton MJ, Clark JM. 1988. Archosaur phylogeny and the relationships of the Crocodylia; pp. 295–338 in MJ. Benton (ed.), The phylogeny and classification of the tetrapods, Vol. 1.
Thrips are generally considered to be the sister group to Hemiptera (bugs). The phylogeny of thrips families has been little studied. A preliminary analysis in 2013 of 37 species using 3 genes, as well as a phylogeny based on ribosomal DNA and three proteins in 2012, supports the monophyly of the two suborders, Tubulifera and Terebrantia. In Terebrantia, Melanothripidae may be sister to all other families, but other relationships remain unclear.
Furthermore, the definition of the clade Crurotarsi would change, as it is often defined by the inclusion of phytosaurs. Thus, Crurotarsi would include phytosaurs and all other archosaurs —including dinosaurs— under this phylogeny. Below is a cladogram showing the placement of phytosaurs from Nesbitt (2011): The phylogenetic analysis of Stocker (2010) placed Paleorhinus outside Phytosauridae as a basal phytosaur. Under this phylogeny, Phytosauridae and Phytosauria are not synonymous.
The phylogenetic position of frogs currently included in the genus Pseudis in relation to other anurans was for a long time a matter of debate. They have been placed in Ranidae, Leptodactylidae,NOBLE, G. K. 1922. The phylogeny of Salientia. I. The osteology and thigh musculature; their bearing on classification and phylogeny. Bulletin of the American Museum of Natural History. 46:1-87. Hylidae,PARKER, H. W. 1935.
Octoknemaceae is a monotypic family of flowering plants endemic to continental Africa. The APG III system of 2009 and the APG II system of 2003 (unchanged from the APG system of 1998), do not recognize this family.Angiosperm Phylogeny Group (2003). An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II. Botanical Journal of the Linnean Society 141(4): 399-436.
The generation of networks required two phases. In the first phase, the researchers devised a number of phylogenies, called candidate trees, to be tested for compatibility. A character is compatible when its origin is explained by the phylogeny generated.. In a perfect phylogeny, all the characters are compatible and the compatibility of the tree is 100%. By the principle of parsimony, or Occam's razor, no networks are warranted.
Triepeolus is a genus of cuckoo bees in the family Apidae. There are at least 140 described species in Triepeolus. Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Ceratina strenua, the nimble ceratina, is a species of carpenter bee in the family Apidae. It is found in North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012. Cladistics 28(1): 80-112.
Cladistics 28(1): 80-112.Ward, P.S. (2007). "Phylogeny, classification, and species-level taxonomy of ants". Zootaxa 1668 549–563Bolton, B., Alpert, G., Ward, S. Naskrecki, P. (2007).
Crabronina is a subtribe of square-headed wasps in the family Crabronidae. There are at least 1,300 described species in Crabronina.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Cladistics 28(1): 80-112.Ward, P.S. (2007). "Phylogeny, classification, and species-level taxonomy of ants". Zootaxa 1668 549–563Bolton, B., Alpert, G., Ward, S. Naskrecki, P. (2007).
Stictiella is a genus of sand wasps in the family Crabronidae. There are at least 14 described species in Stictiella. Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Stictiellina is a subtribe of traditional sphecidae in the family Crabronidae. There are at least 60 described species in Stictiellina. Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Calliopsini is a tribe of mining bees in the family Andrenidae. There are at least 120 described species in Calliopsini. Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
The debate on avian ancestry: phylogeny, function, and fossils. Pages 3–30 in Mesozoic Birds: Above the Heads of Dinosaurs (eds. L. M. Chiappe and L. M. Witmer).
Cladistics 28(1): 80-112.Ward, P.S. (2007). "Phylogeny, classification, and species-level taxonomy of ants". Zootaxa 1668 549–563Bolton, B., Alpert, G., Ward, S. Naskrecki, P. (2007).
Lithurgopsis is a genus of northern cactus woodborers in the family Megachilidae. There are at least nine described species in Lithurgopsis.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Cladistics 28(1): 80-112.Ward, P.S. (2007). "Phylogeny, classification, and species-level taxonomy of ants". Zootaxa 1668 549–563Bolton, B., Alpert, G., Ward, S. Naskrecki, P. (2007).
Cladistics 28(1): 80-112.Ward, P.S. (2007). "Phylogeny, classification, and species-level taxonomy of ants". Zootaxa 1668 549–563Bolton, B., Alpert, G., Ward, S. Naskrecki, P. (2007).
Cladistics 28(1): 80-112.Ward, P.S. (2007). "Phylogeny, classification, and species-level taxonomy of ants". Zootaxa 1668 549–563Bolton, B., Alpert, G., Ward, S. Naskrecki, P. (2007).
Dufourea monardae, the monarda dufourea, is a species of sweat bee in the family Halictidae. It is found in North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Delfino, M., Piras, P., and Smith, T. (2005). Anatomy and phylogeny of the gavialoid crocodylian Eosuchus lerichei from the Paleocene of Europe. Acta Palaeontologica Polonica 50:565–580.
Chen, K.-N. Shen, C. Fu, & P. Borsa. 2012. Genus-level taxonomic changes implied b mitochondrial phylogeny of grey mullets (Teleostei: Mugilidae). Comptes Rendus Biologies, 335: 687-697.
Coptotriche singularis is a moth of the family Tischeriidae. It was described by Stonis and Diškus in 2008.Global diversity; phylogeny of Tischeriidae It is found in Belize.
Its pollen is shed as permanent tetrads.Walker JW (1971) Pollen Morphology, Phytogeography, and Phylogeny of the Annonaceae. Contributions from the Gray Herbarium of Harvard University, 202: 1-130.
The pulp around the seeds is relished by birds. This plant used to belong to the family Flacourtiaceae, but was relocated to Achariaceae by the Angiosperm Phylogeny Group.
Its pollen is shed as permanent tetrads.Walker JW (1971) Pollen Morphology, Phytogeography, and Phylogeny of the Annonaceae. Contributions from the Gray Herbarium of Harvard University, 202: 1-130.
Osteology of Blastomeryx and phylogeny of the American Cervidae. Bulletin of the American Museum of Natural History 24(27):535-562W. K. Gregory. 1910. The orders of mammals.
NIHEI, S.S. & CARVALHO, C.J.B. de. 2007. Phylogeny and classification of Muscini (Diptera, Muscidae). Zoological Journal of the Linnean Society, 149: 493-532. NIHEI, S.S. & CARVALHO, C.J.B. de. 2009.
A molecular phylogeny of the Indo-West Pacific species of Haloa sensu lato gastropods (Cephalaspidea: Haminoeidae): Tethyan vicariance, generic diversity, and ecological specialization. Molecular Phylogenetics and Evolution. 139.
The cladogram is based on molecular phylogeny using mitochondrial (12S, 16S) and nuclear (18S, 28S, and H3) gene markers by Yaron Malkowsky and Annette Klussmann-Kolb in 2012.
Piggin, J., and Bruhl, J.J. (2010). Phylogeny reconstruction of Callitris Vent. (Cupressaceae) and its allies leads to inclusion of Actinostrobus within Callitris. Australian Systematic Botany 23: 69-93.
"A global phylogeny of apple snails: Gondwanan origin, generic relationships, and the influence of outgroup choice (Caenogastropoda: Ampullariidae)". Biological Journal of the Linnean Society 98(1): 61–76. .
Its pollen is shed as permanent tetrads.Walker JW (1971) Pollen Morphology, Phytogeography, and Phylogeny of the Annonaceae. Contributions from the Gray Herbarium of Harvard University, 202: 1-130.
Pecluma is a genus of ferns in the family Polypodiaceae, subfamily Polypodioideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). They are called rockcap ferns.
Stratigraphic positions of chasmosaurine specimens from the Dinosaur Park Formation The following cladogram shows the phylogeny of Chasmosaurus according to a study by Scott Sampson e.a. in 2010.
Teratophyllum is a genus of ferns in the family Dryopteridaceae, subfamily Elaphoglossoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). The genus is native to Malesia.
Phylogeny and classification of the Old World Emberizini (Aves, Passeriformes). Molecular Phylogenetics and Evolution. 47:960-973.Byers, C., U. Olsson and J. Curson. 1995. Sparrows and buntings.
Breviora 464:1–23.Benton, M. J. and J. M. Clark. 1988. Archosaur phylogeny and the relationships of the Crocodylia. pp. 295–338. In M. J. Benton (ed.).
Molecular phylogeny of the hawk-eagles (genus Spizaetus). Zoologische Mededelingen, Leiden, 79(3), 179-180.Amadon, D. (1953). Remarks on the Asiatic hawk‐eagles of the genus Spizaetus.
A molecular phylogeny and generic classification of Asphodelaceae subfamily Alooideae: A final resolution of the prickly issue of polyphyly in the Alooids? Systematic Botany 39(1):55-74.
"Molecular phylogeny of Parnassiinae butterflies (Lepidoptera: Papilionidae) based on the sequences of four mitochondrial DNA segments". Annales de la Société Entomologique de France. (n.s.) 44 (1): 1-36.
Benny Bytebier, Dirk U. Bellstedt, and Hans Peter Linder. 2007. "A molecular phylogeny for the large African orchid genus Disa". Molecular Phylogenetics and Evolution 43(1):75-90.
Macrothelypteris is a genus of ferns in the family Thelypteridaceae, subfamily Phegopteridoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). The genus name means 'large Thelypteris'.
Sparganothina decagramma is a species of moth of the family Tortricidae. It is found in Santa Catarina, Brazil.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
Oxford University Press. . but they are now usually considered separate species.Helbig, A. J. (2001). Phylogeny and biogeography of the genus Sylvia, in: Shirihai, Hadoram: Sylvia warblers: 24-29.
Systematic Botany 38(1), 253-58.Schilling, E. E., et al. (2015). Bricklebush (Brickellia) phylogeny reveals dimensions of the great Asteraceae radiation in Mexico. Molecular Phylogenetics and Evolution.
Arbour VM, Currie PJ. 2016. Systematics, phylogeny and palaeobiogeography of the ankylosaurid dinosaurs. Journal of Systematic Palaeontology 14: 385–444. Being Emausaurus and Scutellosaurus more basal than Scelidosaurus.
How much data are needed to resolve a difficult phylogeny? Case study in Lamiales. Systematic Biology 54: 697–709. and 2007, based on phylogenetic analyses of genetic material.
Although most research on the phylodynamics of influenza has focused on seasonal influenza A/H3N2 in humans, influenza viruses exhibit a wide variety of phylogenetic patterns. Qualitatively similar to the phylogeny of influenza A/H3N2's hemagglutinin protein, influenza A/H1N1 exhibits a ladder-like phylogeny with relatively low genetic diversity at any point in time and rapid lineage turnover. However, the phylogeny of influenza B's hemagglutinin protein has two circulating lineages: the Yamagata and the Victoria lineage. It is unclear how the population dynamics of influenza B contribute to this evolutionary pattern, although one simulation model has been able to reproduce this phylogenetic pattern with longer infectious periods of the host.
Reasons for investigating the origins of the Pyrobombus bees can be due to questionable physical resemblance between the species and enzymes. Some studies of the Pyrobombus phylogeny concludes this subgenus may not be monophyletic and is instead polyphyletic, where it shares multiple evolutionary ancestors, however, it is argued results that lead for the nature of the Pyrobombus to be polyphyletic may be due to a smaller taxon representation. In the study by Hines, Cameron and Williams, they have gathered a larger taxon representation to investigate the phylogeny of the Pyrobombus, and conclude that the phylogeny of the subgenus; Pyrobombus to be monophyletic. They were able to analyze 36 of the 43 recognized species.
A common protein that derives from one of the phylogeny branches of FtsK is SpoIIIE which is essential during chromosome segregation. FtsK is found in most bacteria including E. coli , Staphyloccus, and Streptomycetes and in a select amount of Archaea and the phylogenetic tree is similar to that of bacteria. However the difficulty within exact dating of the diversification within its phylogeny is that proteins have variety in their branch lengths which makes it difficult to follow an exact timeline. The phylogeny of FtsK can therefore be compared to the time that protein groups VirB4/VirD4 diversified and slightly earlier than TraB and TcpA as they only occur in Actinobacteria and Firmicutes.
CRAVEIRO S.C., PANDEIRADA M.S., DAUGBJERG N., MOESTRUP Ø. AND CALADO A.J. 2013. Ultrastructure and phylogeny of Theleodinium calcisporum gen. et sp. nov., a freshwater dinoflagellate that produces calcareous cysts.
Andrena palpalis is a species of mining bees in the family Andrenidae. It is found in Central America and North America. Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Triepeolus grandis is a species of cuckoo bees in the family Apidae. It is found in Central America and North America. Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Cladistics 28(1): 80-112. Ward, P.S. (2007). "Phylogeny, classification, and species-level taxonomy of ants". Zootaxa 1668 549–563 Bolton, B., Alpert, G., Ward, S. Naskrecki, P. (2007).
Crabro cingulatus is a species of square-headed wasp in the family Crabronidae. It is found in Central America and North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
This phylogeny is supported by several molecular studies. Other researchers state that taking fossils into account leads to different conclusions, for example that the ferns (Pteridophyta) are not monophyletic.
Molecular Phylogeny Estimation of the Bamboo Genus Chusquea (Poaceae: Bambusoideae: Bambuseae) and Description of Two New Subgenera. Systematic Botany, 39(3). ;SpeciesClark, L. G. 2000. Chusquea. 39: 36–52.
Vandenboschia is a fern genus in the family Hymenophyllaceae. The genus is accepted in the Pteridophyte Phylogeny Group classification of 2016 (PPG I) but not by some other sources.
Polyphlebium is a fern genus in the family Hymenophyllaceae. The genus is accepted in the Pteridophyte Phylogeny Group classification of 2016 (PPG I) but not by some other sources.
Sewardiella is a genus of liverwort in the family Petalophyllaceae.Crandall- Stotler, B.J., Stotler, R.E., and Long, D.G. 2009. Phylogeny and classification of the Marchantiophyta. Edinburgh Journal of Botany, vo.
Flora of North America. Some authors consider the two plants to be one species.Rönblom, K. and A. A. Anderberg. (2002). Phylogeny of Diapensiaceae based on molecular data and morphology.
Archiheterodonta is an infraclass of bivalve molluscs.Giribet G. 2008. Bivalvia. Pp. 105-141, in: Ponder W.F. & Lindberg D.L. (eds), Molluscan Phylogeny. Berkeley: University of California Press, xi+469 pp.
An alternative phylogeny of spermatophytes based on the work by Novíkov & Barabaš-Krasni 2015 with plant taxon authors from Anderson, Anderson & Cleal 2007 showing the relationship of extinct clades.
Guo, Y. and S. Ge. (2005). Molecular phylogeny of Oryzeae (Poaceae) based on DNA sequences from chloroplast, mitochondrial, and nuclear genomes. American Journal of Botany 92(9) 1548-58.
Some consider the Myxomycota to be a separate kingdom, with an unsettled phylogeny because of conflicting molecular and developmental data. The relations among Myxogastrid orders are as yet unclear.
The species name refers to the presence of setae on the uncus dorsally and is derived from Latin setosus (meaning bristly).Systematics and phylogeny of Sparganothina and related taxa.
The species name refers to the habitus similarity between this species and Sparganothina amoebaea, with the Greek prefix neos (meaning new).Systematics and phylogeny of Sparganothina and related taxa.
Armen L. Takhtajan (Takhtadzhian). Flowering Plants second edition (2009). Springer Science+Business Media. . Successive revisions of the Angiosperm Phylogeny Group (APG) classification have changed the circumscription of the family.
Carpenter, James. Strassmann, Joan. The phylogeny of the social wasp subfamily Polistinae: evidence from microsatellite flanking sequences, mitochondrial COI sequence, and morphological characters. BMC Evolutionary Biology 2004, 4:8.
Australasian Bulimulidae: Bothriembryon, Placostylus. Helicidae: Amphidromus. 253 pp., 72 plates. Breure (1979)Breure A.S. H. (1979) "Systematics, phylogeny and zoogeography of Bulimulinae (Mollusca)". Zoologische Verhandelingen Leiden 168: 1-215.
At first H. scholtzi was mistakenly classified as a diapsid.Benton, M. J. 1985. Classification and phylogeny of the diapsid reptiles. Zoological Journal of the Linnean Society 84:97–164.
Niphidium is a genus of ferns in the family Polypodiaceae, subfamily Polypodioideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). They are native to tropical America.
"The phylogeny of squamate reptiles (lizards, snakes and amphisbaenians) inferred from nine nuclear protein-coding genes". Comptes Rendus Biologies 328 (10-11): 1000-1008. Gorman GC, Gress F (1970).
The following phylogeny of Fejervarya is from Pyron & Wiens (2011). 7 species are included. Fejervarya is a sister group of Zakerana, which had until recently been included in Fejervarya.
Dunz, A.R., and Schliewen, U.K. (2013). Molecular phylogeny and revised classification of the haplotilapiine cichlid fishes formerly referred to as “Tilapia”. Molecular Phylogenetics and Evolution, online 29 March 2013.
"A molecular phylogeny of the Cephalaspidea sensu lato (Gastropoda: Euthyneura): Architectibranchia redefined and Runcinacea reinstated". Zoologica Scripta 38(1): 23-41. . It has been classified in the superfamily Diaphanoidea.
Pyron, R. Alexander; Burbrink, Frank T.; Wiens, John J. (2013). "A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes". BMC Evolutionary Biology 13: 93.
A more recent alternate phylogeny, by Norman in 2014, resolved a monophyletic Hypsilophodontia (the family Hypsilophodontidae was not used because of its history). Hypsilophodon grouped with Rhabdodontidae and Tenontosaurus.
Hensmania is a genus of herbs in the family Asphodelaceae,Stevens, P.F. (2001 onwards). "Hemerocallidoideae". Angiosperm Phylogeny Website. Retrieved 2016-06-10. first described as a genus in 1903.
Its closest relative is Amphorogyne, also endemic to New Caledonia.Der, J. P., and D. L. Nickrent. (2008. A Molecular Phylogeny of Santalaceae (Santalales).” Systematic Botany 33 (1): 107–16.
The cladogram below shows the phylogeny (progeny or offspring) of Machali with code names and/or nicknames. From 1999 to 2006, she gave birth to at least 11 cubs.
An alternative, more statistically justified approach to assess alignment uncertainty is the use of probabilistic evolutionary models for joint estimation of phylogeny and alignment. A Bayesian approach allows calculation of posterior probabilities of estimated phylogeny and alignment, which is a measure of the confidence in these estimates. In this case, a posterior probability can be calculated for each site in the alignment. Such an approach was implemented in the program BAli-Phy.
This clade that had resulted repeatedly in molecular studies with still limited "lower heterobranch" taxon sampling, either in a derived position or as a basal offshoot within Euthyneura. A recent molecular phylogeny on Acteonoidea suggest a common origin with lower heterobranch Rissoelloidea and a sister group relationship to Nudipleura.Gbbeler K. & Klussmann-Kolb A. (2010). "The phylogeny of the Acteonoidea (Gastropoda): molecular systematics and first detailed morphological study of Rictaxis punctocaelatus (Carpenter, 1864)".
Molecular phylogenetic analysis demonstrated that the vittarioid ferns were nested within the genus Adiantum as it was originally circumscribed, making that genus paraphyletic. In the Pteridophyte Phylogeny Group classification of 2016 (PPG I), the family is treated as the subfamily Vittarioideae] of the family Pteridaceae. The following diagram shows a likely phylogenetic relationship between the Vittarioideae and other subfamilies of the Pteridaceae.Schuettpelz & Pryer (2008) "Fern phylogeny" in Biology and Evolution of Ferns and Lycophytes, ed.
Christin, P., et al. (2010). Can phylogenetics identify C4 origins and reversals? Trends in Ecology and Evolution 25(7): 403–09.Grass Phylogeny Working Group II. (2012). New grass phylogeny resolves deep evolutionary relationships and discovers C4 origins. New Phytologist 193(2): 304–12. . Secondly, that there was a single origin of C4 photosynthesis within the genus, and the C3 taxon, A. s. ecklonia, was subsequently derived from a C4 ancestor (the reversion hypothesis).
1960 reprint of 1942 publication. Anthodon has not yet been sampled for DNA, but four of its close relatives, Hippocratea, Pristimera, Plagiopteron, and Loesenerella were sampled for a molecular phylogeny of Celastraceae that was published in 2008.Mark P. Simmons, Jennifer J. Cappa, Robert H. Archer, Andrew J. Ford, Dedra Eichstedt, and Curtis C. Clevinger (2008). "Phylogeny of the Celastreae and the relationships of Catha edulis inferred from morphological characters and nuclear and plastid genes".
Plant taxonomy systematists currently favor the APG IV system of 2016 over the older Cronquist system for classifying flowering plants (Angiosperms). The 2009 APG III system assigned the first two families to the order Caryophyllales and the last family to the order Ericales.Angiosperm Phylogeny Group (2003). An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II. Botanical Journal of the Linnean Society 141(4): 399-436.
It is also the only published phylogeny that includes V. polylepis. As with the most recent morphological phylogeny, it too shows that the groups Aphyllae and Foliosae are not true evolutionary groups. The genus is instead divided into three subgroups, which the authors have named alpha, beta and gamma. These groups seem to reflect geographical distributions, with alpha containing American membranous species, beta American fragrant species and gamma the old world and Caribbean species.
The Darwinian Revolution. Chicago: University of Chicago Press. Embryology theories of Ernst Haeckel and Karl Ernst von Baer compared Haeckel advanced a version of the earlier recapitulation theory previously set out by Étienne Serres in the 1820s and supported by followers of Étienne Geoffroy Saint- Hilaire including Robert Edmond Grant. It proposed a link between ontogeny (development of form) and phylogeny (evolutionary descent), summed up by Haeckel in the phrase "ontogeny recapitulates phylogeny".
Barbeuia madagascariensis, a plant for which the family Barbeuiaceae was created, based on molecular data obtained by Cuénoud. Cuénoud studied the phylogeny of the genus Ilex (hollies and related species, Aquifoliaceae) with Jean-François Manen, Pierre-André Loizeau and Rodolphe Spichiger,Cuénoud, P., Del Pero Martinez M.A., Loizeau P.-A., Spichiger, R., Andrews S., Manen J.-F. (2000). Molecular phylogeny and biogeography of the genus Ilex L. (Aquifoliaceae). Annals of Botany, 85: 111-122.
The increase in high quality mammalian reference sequences generally makes comparative analysis better as it increases statistical power. However, the increase in number of species in a phylogeny does risk adding unnecessary noise as the alignments of the orthologous sequences usually decrease in quality. Furthermore, different classes of species will have significant differences in their phenotypes. Despite this, comparative genomics has allowed us to connect the genetic changes found in a phylogeny to specific pathways.
However, this is not to say that a taxon at any other rank may not be sharply defined, or that any species is guaranteed to be sharply defined. It varies from case to case. Ideally, a taxon is intended to represent a clade, that is, the phylogeny of the organisms under discussion, but this is not a requirement. A classification in which all taxa have formal ranks cannot adequately reflect knowledge about phylogeny.
"Physiological significance of sulci in somatic sensory cerebral cortex in mammals of the family Procyonidae." Journal of Comparative Neurology 120.1 (1963): 19-36. Ursidae,O'brien, Stephen J., et al. "A molecular solution to the riddle of the giant panda's phylogeny." (1985): 140-144.Eichelberger MA, Wildt DE, Bush M (1985) Constructing a molecular phylogeny of the giant panda (Ailuropoda melanoleuca). Bongo (Berlin) 10, 175–182.Pastor, J. F., M. Barbosa, and F. J. De Paz.
Molecular phylogeny and morphology of Haplozoon ezoense n. sp. (Dinophyceae): A parasitic dinoflagellate with ultrastructural evidence of remnant non-photosynthetic plastids. Protist, 169(3), 333-350. doi: 10.1016/j.protis.2018.04.
Sachs S. 2005. Tuarangisaurus australis sp. nov. (Plesiosauria: Elasmosauridae) from the Lower Cretaceous of northeastern Queensland, with additional notes on the phylogeny of the Elasmosauridae. Memoirs of the Queensland Museum.
S. Bi, X. Jin, S. Li and T. Du. 2015. A new Cretaceous metatherian mammal from Henan, China. PeerJ 3:e896 The most recent phylogeny including Pappotherium is reproduced below.
This family was previously sometimes known as Vexillidae. Latiromitra (from family Ptychatractidae) has been found to be closely related to Costellariidae in the molecular phylogeny analysis by Fedosov & Kantor (2010).
Geitonoplesium is a genus of a sole species Geitonoplesium cymosum, the scrambling lily. It is a member of the family Asphodelaceae, subfamily Hemerocallidoideae.Stevens, P.F. (2001 onwards). "Hemerocallidoideae". Angiosperm Phylogeny Website.
The Monimiaceae is a family of flowering plants in the magnoliid order Laurales.Peter F. Stevens (2001 onwards). "Monimiaceae" At: Angiosperm Phylogeny Website. At: Botanical Databases At: Missouri Botanical Garden Website.
Another choice is to divide the family into many genera, one of which is Thelypteris. This is the approach taken in the Pteridophyte Phylogeny Group classification of 2016 (PPG I).
L. vierecki is part of tribe Halictini, which is made up of over 2000 species.Danforth, B. N. et al. (2008). "Phylogeny of Halictidae with emphasis on endemic African Halictinae" (PDF).
Susy Fuentes-Bazan, Pertti Uotila, Thomas Borsch: A novel phylogeny-based generic classification for Chenopodium sensu lato, and a tribal rearrangement of Chenopodioideae (Chenopodiaceae). In: Willdenowia 42, 2012, p. 18.
Petalophyllum ralfsii, the petalwort, is a liverwort of the order Fossombroniales.Crandall-Stotler, B.J., Stotler, R.E. and Long, D.G. 2009. Phylogeny and classification of the Marchantiophyta. Edinburgh Journal of Botany, vo.
"Phylogeny, genome size, and chromosome evolution of Asparagales". Aliso 22(Monocots: Comparative Biology and Evolution):287-304. ISSN 0065-6275. Recent treatments have divided Brodiaeoideae (or Themidaceae) into 12 genera.
The Schistosomatoidea are a superfamily of digenetic trematodes.Snyder, S. D. (2004). Phylogeny and paraphyly among tetrapod blood flukes (Digenea: Schistosomatidae and Spirorchiidae). International Journal for Parasitology 34(12), 1385-92.
Abedinia, M., et al. (1998). Distribution and phylogeny of Potamophila parviflora R.Br., a wild relative of rice from eastern Australia. Genetic Resources and Crop Evolution 45 399-406.Genus Potamophila.
Previously this genus was placed within the subfamily Bulimulinae.Breure A. S. H. (1979). "Systematics, phylogeny and zoogeography of Bulimulinae (Mollusca)". Zoologische Verhandelingen Leiden 168: 1-215, figs 1-182, pls.
Campyloneurum is a genus of ferns in the family Polypodiaceae, subfamily Polypodioideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). They are commonly known as strap ferns.
The species name refers to the shape of the apex at the aedeagus and is derived from Latin cultratus (meaning knife shaped).Systematics and phylogeny of Sparganothina and related taxa.
Zoogeographical history of African crocodilians since the Triassic. In: Karl L. Schuchmann, ed., Proceedings of the International Symposium on African Vertebrates: Systematics, Phylogeny and Evolutionary Ecology. pp. 453-469. Bonn.
Susy Fuentes-Bazan, Pertti Uotila, Thomas Borsch: A novel phylogeny-based generic classification for Chenopodium sensu lato, and a tribal rearrangement of Chenopodioideae (Chenopodiaceae). In: Willdenowia 42, 2012, p. 17.
Gastropods on Land: Phylogeny, Diversity and Adaptive Morphology. in Barker G. M. (ed.): The biology of terrestrial molluscs. CABI Publishing, Oxon, UK, 2001, . 1-146, cited pages: 139 and 142.
Reineckeiidae is an extinct ammonoid cephalopod family belonging to the superfamily Perisphinctoidea.Mikko's Phylogeny Archive These fast-moving nektonic carnivores lived during the Jurassic period, from the Callovian to the Oxfordian.
Mammalian species, (495), 1-11.Wootton, J. T. (1987). The effects of body mass, phylogeny, habitat, and trophic level on mammalian age at first reproduction. Evolution, 41(4), 732-749.
Archigrammitis is a genus of ferns in the family Polypodiaceae, subfamily Grammitidoideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). It is known from Malesia and Polynesia.
Euchariomyia dives is a species of fly in the subfamily Bombyliinae.Li, Xuankun & Yeates, David. (2019). Phylogeny, classification and biogeography of bombyliine bee flies (Diptera, Bombyliidae). Systematic Entomology. 10.1111/syen.12361.
Rheinischen Friedrich-Wilhelms- Universität Bonn.Dunz; and Schliewen (2013). Molecular phylogeny and revised classification of the haplotilapiine cichlid fishes formerly referred to as Tilapia. Molecular Phylogenetics and Evolution 68: 64-80.
Alexander Hanchett Smith (December 12, 1904 – December 12, 1986) was an American mycologist known for his extensive contributions to the taxonomy and phylogeny of the higher fungi, especially the agarics.
Brusatte, S. L., & Carr, T. D. (2016). The phylogeny and evolutionary history of tyrannosauroid dinosaurs. Scientific Reports, 6. Below is a cladogram placing Coelurus in Coelurosauria by Cau et al.
Marivaux et al.Marivaux, L., M. Vianey- Liaud, and J.-J. Jaeger. 2004. High-level phylogeny of early Tertiary rodents: dental evidence. Zoological Journal of the Linnean Society, 142:105-134.
Benny Bytebier, Dirk U. Bellstedt, and Hans Peter Linder. 2008. "A New Phylogeny-Based Sectional Classification for the Large African Orchid Genus Disa". Taxon 57(4):1233-1251. 19 pages.
The species name refers to the colour of the species and is derived from Latin aureolis (meaning golden, splendid).Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
The species name refers to the colour of the species and is derived from Latin flammeus (meaning flame, fire)Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
The Carcinosomatoidea have a poorly resolved internal phylogeny, though can be easily recognised by scorpion-like appearance and heavily spinose appendages. Numerous characteristics support a close relationship to the Eurypteroidea.
Albrecht, A. (1990): Revision, phylogeny and classification of the genus Dorylomorpha (Diptera, Pipunculidae). Acta Zoologica Fennica 188: 1-240; Helsinki.Coe, R.L. (1966) Pipunculidae.Handbook for the Identification of British Insects, Vol.
Mycopteris is a genus of ferns in the family Polypodiaceae, subfamily Grammitidoideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). It is known from the American tropics.
This is an incomplete list of prehistoric mammals. It does not include extant mammals or recently extinct mammals. For extinct primate species, see: list of fossil primates.Mikko's Phylogeny Archive Paleofile.
"Molecular phylogeny of the softshell turtle genus Nilssonia revisited, with first records of N. formosa for China and wild-living N. nigricans for Bangladesh." Vertebrate Zoology 62.2 (2012): 261-272.
Chortolirion (Gk. 'chortos' = 'pasture', 'lirion' ='lily') is a genus of perennial plants in the family Asphodelaceae, subfamily Asphodeloideae,Stevens, P.F. (2001 onwards). "Asphodeloideae". Angiosperm Phylogeny Website. Retrieved 2016-06-10.
Accessed through: World Register of Marine Species on 2016-11-14.Brunckhorst D.J. (1993) The systematics and phylogeny of phyllidiid nudibranchs (Doridoidea). Records of the Australian Museum suppl. 16: 1-108.
221-280(60) The genus is accepted in the Pteridophyte Phylogeny Group classification of 2016 (PPG I), but not by some other sources which sink it into a broadly defined Trichomanes.
Trypoxylon collinum larva Trypoxylini is a tribe of traditional Sphecidae in the family Crabronidae. There are at least 840 described species in Trypoxylini. Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Biastini is a tribe of cuckoo bees in the family Apidae. There are at least 3 genera and about 12 described species in Biastini.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Tandrange (Nepali: Tāndrāṅe; IPA: tandraŋe) is a Sino-Tibetan language spoken in a few ethnic Gurung villages of Lamjung District, Nepal.Schorer, Nicolas. 2016. The Dura Language: Grammar and Phylogeny. Leiden: Brill.
Shonisauridae is an early group of ichthyosaurs, living in the late Triassic period.Maisch, M.W. (2010). "Phylogeny, systematics, and origin of the Ichthyosauria – the state of the art." Palaeodiversity, 3: 151–214.
Bjerring, H. C. (1985). Facts and thoughts on piscine phylogeny. In: Evolutionary Biology of Primitive Fishes (eds. R. E. Foreman, A. Gorbman, J. M. Dodd och R. Olsson), pp. 31-57.
The classification of ferns has been completely overhauled in that time.Eric Schuettpelz and Kathleen M. Pryer. 2008. "Fern phylogeny" pages 395-416. In: Tom A. Ranker and Christopher H. Haufler (editors).
The hindwings are white to very light gray., 2006: Phylogeny and life history evolution of Prodoxus yucca moths (Lepidoptera: Prodoxidae). Systematic Entomology 31: 1-20. Adults are on wing in April.
Yoshihisa Taguchi's (2012) computational phylogenetic study classifies the Mienic languages as follows.Yoshihisa Taguchi [田口善久] (2012). On the Phylogeny of the Hmong-Mien languages . Conference in Evolutionary Linguistics 2012.
Journal of Vertebrate Paleontology 12:93–102.Gower, D. J. (1996). The tarsus of erythrosuchid archosaurs, and implications for early diapsid phylogeny. Zoological Journal of the Linnean Society 116:347–375.
The following phylogeny of Polypedates is from Pyron & Wiens (2011). 8 species are included. Polypedates is a sister group of Feihyla. Together, Polypedates and Feihyla form a sister group to Rhacophorus.
The genus Pilophorus was until recently considered to be a member of the family Stereocaulaceae by some authors.Tehler A. (1996). 1996. Systematics, phylogeny and classification. In T. H. Nash III [ed.
Drepaninae are by far the largest subfamily of the Drepanidae moths. While it is usually split into two tribes, Drepanini and Oretini, its internal systematics and phylogeny are not well resolved.
Its pollen is shed as permanent tetrads.Walker JW (1971) Pollen Morphology, Phytogeography, and Phylogeny of the Annonaceae. Contributions from the Gray Herbarium of Harvard University, 202: 1-130. Cananga odorata var.
Petalophyllum, or petalwort, is a genus of liverworts in the order Fossombroniales.Crandall-Stotler, B.J., Stotler, R.E., and Long, D.G. 2009. Phylogeny and classification of the Marchantiophyta. Edinburgh Journal of Botany, vo.
The pollen of G. curtisii is shed as permanent tetrads.Walker JW (1971) Pollen Morphology, Phytogeography, and Phylogeny of the Annonaceae. Contributions from the Gray Herbarium of Harvard University, 202: 1-130.
The species name refers to the transtilla, which bears three sets of stripes and is derived from Latin ternarius (meaning consisting of three).Systematics and phylogeny of Sparganothina and related taxa.
J. Moll. Stud. 67: 215–224.Oliverio M. M. Cervelli, and P. Mariottini. 2002. ITS2 rRNA evolution and its congruence with the phylogeny of muricid neogastropods (Caenogastropoda, Muricoidea) Mol. Phylogenet. Evol.
To resolve a well-supported eumalacostracan phylogeny and obtain a robust tree, it will be necessary to look beyond the most commonly utilized sources of data (nuclear ribosomal and mitochondrial sequences).
Arthrobotrya is a genus of ferns in the family Dryopteridaceae, subfamily Elaphoglossoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). The genus is native to Australia and New Zealand.
Dracoglossum is a small genus of ferns in the family Lomariopsidaceae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). It is native to the Neotropics of the Americas.
The currently accepted taxonomy is based on the phylogeny is based on 16S rRNA-based LTP release 106 by 'The All-Species Living Tree' Project 'The All-Species Living Tree' Project.
The origin of the genus Hemidactylus is still unclear as the higher level phylogeny is not well resolved. Moreover, much of the diversity in this group still remains to be discovered.
Gudrun Kadereit, Thomas Borsch, K. Weising, and Helmut Freitag (2003): Phylogeny of Amaranthaceae and Chenopodiaceae and the evolution of C4 photosynthesis. - In: Int. J. Plant Sci. 164(6): p. 959–986.
She also published many papers on avian taxonomy and phylogeny as well as writing extensive sections of The Birds of the USSR (1951–1953) and the series Fauna of the USSR.
P. C. Sereno. 2012. Taxonomy, morphology, masticatory function and phylogeny of heterodontosaurid dinosaurs. Zookeys 226:1-225 [M. Carrano/M. Carrano] It was around tall and around long when fully grown.
Elizabeth H. Zacharias, Bruce G. Baldwin (2010): A Molecular Phylogeny of North American Atripliceae (Chenopodiaceae), with Implications for Floral and Photosynthetic Pathway Evolution. In: Systematic Botany 35(4), p.839-857.
The phylogeny of larks (Alaudidae) was reviewed by Alström et al. (2013) who found that the following species form a well supported monophyletic group, which is the sister lineage to Heteromirafra.
Sparganothina nephela is a species of moth of the family Tortricidae. It is found in Nicaragua, Costa Rica, Panama and Ecuador.Systematics and Phylogeny of Sparganothina and Related Taxa (Lepidoptera: Tortricidae: Sparganothini).
Stawellia is a genus of herbs in the family Asphodelaceae, subfamily Hemerocallidoideae,Stevens, P.F. (2001 onwards). "Hemerocallidoideae". Angiosperm Phylogeny Website. Retrieved 2016-06-10. first described as a genus in 1870.
Pasithea is a genus of herbs in the family Asphodelaceae, subfamily Hemerocallidoideae,Stevens, P.F. (2001 onwards). "Hemerocallidoideae". Angiosperm Phylogeny Website. Retrieved 2016-06-10. first described as a genus in 1832.
Molecular phylogeny of the Cheilodactylidae and Latridae (Perciformes: Cirrhitoidea) with notes on taxonomy and biogeography. Molecular Phylogenetics and Evolution 30: 118–127Randall (2007). Reef and Shore Fishes of the Hawaiian Islands.
A simple cladogram showing the evolutionary relationships between four species: A, B, C, and D. Here, Species A is the outgroup, and Species B, C, and D form the ingroup. In cladistics or phylogenetics, an outgroup is a more distantly related group of organisms that serves as a reference group when determining the evolutionary relationships of the ingroup, the set of organisms under study, and is distinct from sociological outgroups. The outgroup is used as a point of comparison for the ingroup and specifically allows for the phylogeny to be rooted. Because the polarity (direction) of character change can be determined only on a rooted phylogeny, the choice of outgroup is essential for understanding the evolution of traits along a phylogeny.
Phylogeny in psychoanalysis is the study of the whole family or species of an organism in order to better understand the pre-history of it.Sigmund Freud, Wolfman, Penguin Books, Great Ideas, P113 It might have an unconscious influence on a patient, according to Sigmund Freud. After the possibilities of ontogeny, which is the development of the whole organism viewed from the light of occurrences during the course of its life,Sigmund Freud, Wolfman, Penguin Books, Great Ideas, P112 have been exhausted, phylogeny might shed more light on the pre-history of an organism. The term phylogeny derives from the Greek terms phyle (φυλή) and phylon (φῦλον), denoting “tribe” and “race”; and the term genetikos (γενετικός), denoting “relative to birth”, from genesis (γένεσις) “origin” and “birth”.
For example, consider a phylogeny recovered for a genus of plants containing 6 species A - F, where each plant is pollinated by either a "bee", "hummingbird" or "wind". One obvious question is what the pollinators at deeper nodes were in the phylogeny of this genus of plants. Under maximum parsimony, an ancestral state reconstruction for this clade reveals that "hummingbird" is the most parsimonious ancestral state for the lower clade (plants D, E, F), that the ancestral states for the nodes in the top clade (plants A, B, C) are equivocal and that both "hummingbird" or "bee" pollinators are equally plausible for the pollination state at the root of the phylogeny. Supposing we have strong evidence from the fossil record that the root state is "hummingbird".
Below is a cladogram modified from Benton (2004) showing this phylogeny: In Sterling Nesbitt's 2011 monograph on early archosaurs, a phylogenetic analysis found strong support for phytosaurs falling outside Archosauria. Many subsequent studies supported this phylogeny. Because Crurotarsi is defined by the inclusion of phytosaurs, the placement of phytosaurs outside Archosauria means that Crurotarsi must include all of Archosauria. Nesbitt reinstated Pseudosuchia as a clade name for crocodile-line archosaurs, using it as a stem-based taxon.
The phylogeny of the Caelifera, is described in detail for grasshoppers, with 6 out of 8 extant superfamilies shown here as a cladogram. Like the Ensifera, Caelifera and all of its superfamilies appear to be monophyletic. The phylogeny of the Caelifera, based on mitochondrial ribosomal RNA of thirty-two taxa in six out of seven superfamilies, is shown as a cladogram. The Ensifera, Caelifera and all the superfamilies of grasshoppers except Pamphagoidea appear to be monophyletic.
This was based on two synapomorphies, regarding the shape and placement of the teeth. Bonaparte, Bakker, and Paul argued that ornithischians were descended from basal sauropodomorphs, with segnosaurs being transitional taxa as depicted in the phylogeny below. The Phytodinosauria hypothesis is not supported by current data: most phylogenies maintain a monophyletic Saurischia. In such a phylogeny therizinosaurs are maniraptoran dinosaurs more closely related to birds, and any similarity between sauropodomorphs and ornithischians is due to convergence.
They based their resulting phylogeny on characters representing cranial, post- cranial, and osteodermal anatomy, and details of synapomorphies for each recovered clade. This study placed Gargoyleosaurus and Gastonia within basal Nodosauridae, and put Cedarpelta and Liaoningosaurus as basal ankylosaurids. Most recently, Arbour and Currie have presented a phylogenetic analysis of Ankylosauridae consisting of Gastonia, Cedarpelta, Chuanqilong, other basal ankylosaurids, and a number of derived ankylosaurids. Their phylogeny includes some uncertain phylogenetic relationships, between Ankylosaurus, Anodontosaurus, Scolosaurus, and Ziapelta.
Occurrences of fleas on reptiles is accidental, and fleas have been known to feed on the hemolymph (bloodlike body fluid) of ticks. Flea phylogeny was long neglected, the discovery of homologies with the parts of other insects being made difficult by their extreme specialization. Whiting and colleagues prepared a detailed molecular phylogeny in 2008, with the basic structure shown in the cladogram. The Hectopsyllidae, including the harmful chigoe flea or jigger, is sister to the rest of the Siphonaptera.
By 1987, both Ahlquist and Sibley had left Yale. In 1988, Ahlquist and Sibley were awarded the Daniel Giraud Elliot Medal by the National Academy of Sciences. In January 1991 (often listed as 1990), Charles Sibley and Ahlquist published Phylogeny and Classification of Birds, which presented a new phylogeny for birds based on DNA-DNA hybridisation techniques, known as the Sibley-Ahlquist taxonomy. At that time, he was an associate professor of zoology at Ohio University.
In contrast, a more balanced phylogeny may occur when a virus is not subject to strong immune selection or other source of directional selection. An example of this is the phylogeny of the HIV envelope protein inferred from sequences isolated from different individuals in a population (balanced tree). phylogenies of the HIVf envelope protein from chronically infected hosts resemble influenza's ladder-like tree. This highlights that the processes affecting viral genetic variation can differ across scales.
Analysis of 18S and 28S rRNA sequence data, though, suggests that they form the most ancient lineage of springtails, which would explain their peculiar apomorphies. This phylogenetic relationship was also confirmed using a phylogeny based on mtDNA and whole-genome data. The latest whole-genome phylogeny supporting four orders of collembola: Springtails are attested to since the Early Devonian. The fossil from , Rhyniella praecursor, is the oldest terrestrial arthropod, and was found in the famous Rhynie chert of Scotland.
"Phylogeny and Delimitation of the Celastrales Inferred from Nuclear and Plastid Genes". Systematic Botany 31(1):122-137. This study also showed strong support for a pentatomy consisting of Pottingeria, Mortonia, Parnassiaceae, and two clades of genera from Celastraceae as that family had been circumscribed in APG II. The relationships between these five clades remain unresolved. In 2009, the Angiosperm Phylogeny Group expanded the family Celastraceae to consist of the five clades of the pentatomy mentioned above.
Professor Wang specializes in the fossil evolution, systematics, and phylogeny of mammals of the Cenozoic. He has researched the biostratigraphy of Inner Mongolia and Asia as a whole, the geochronology of Asia, paleoenvironments of the Tibetan Plateau, and mammalian migrations between Eurasia and North America. Wang has also investigated the systematics and phylogeny of canids (dogs and their kin) as well as Late Eocene through Pleistocene fossil mammals of Southern California and Mexico. (see Natural History Museum of LA).
In addition to a series of lobe-finned fishes, they also include some of the early labyrinthodonts. Exactly what labyrinthodonts are in the stem group tetrapods rather than the corresponding crown group is uncertain, as the phylogeny of early tetrapods is not well understood. This example shows that crown and stem group definitions are of limited value when there is no consensus phylogeny. Stem arthropods constitute a group that has seen attention in connection with the Burgess Shale fauna.
Benson attributed this revised phylogeny to the inclusion of postcranial characteristics, or features of the skeleton other than the skull, in his analysis. When only cranial or skull features were included, Caseasauria remained the most basal synapsid clade. Below is a cladogram modified from Benson's analysis (2012): However, more recent examination of the phylogeny of basal synapsids, incorporating newly described basal caseids and eothyridids, returned Caseasauria to its position as the sister to all other synapsids. Brocklehurst et al.
FtsK is part of the AAA motor ATPases. The phylogeny tree of FtsK ties back to the split between ssDNA and dsDNA translocases where TraB, FtsK, T4CPs and VirB4s arise. Each of these show structural similarities and the parent branch of FtsK arose along with other branches of TraB, TcpA, and FtsK. Although FtsK has its own phylogeny specifications and branches within, TraB is similar to a sister protein branch that can trace back to the timeline of FtsK.
These two species are not closely related, however, and are likely to be separated in different genera.Weibel, Amy C. & Moore, William S. (2005): Plumage convergence in Picoides woodpeckers based on a molecular phylogeny, with emphasis on convergence in downy and hairy woodpeckers. Condor 107(4): 797–809. (HTML abstract)Moore, William S.; Weibel, Amy C. & Agius, Andrea (2006): Mitochondrial DNA phylogeny of the woodpecker genus Veniliornis (Picidae, Picinae) and related genera implies convergent evolution of plumage patterns. Biol.
Contributions to Zoology solicits high-quality papers in all systematics-related branches of comparative zoology (including paleozoology). Preference is given to manuscripts dealing with conceptual issues and to integrative papers (e.g., ecology and biodiversity, morphology and phylogeny and character state evolution, phylogeny and historical biogeography, systematics and bioinformatics, bioinformatics and biodiversity, habitat disturbance and biogeography, etc.). Reviews and alpha-taxonomic contributions are considered for publication, but acceptance will depend on their high quality and exceptional nature.
Ectemnius cephalotes is a species of square-headed wasps in the family Crabronidae. It is found in Europe & Northern Asia (excluding China) and North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Coptotriche lucida is a moth of the family Tischeriidae. It was described by Annette Frances Braun in 1972.Global diversity; phylogeny of Tischeriidae It is found in the US state of Florida.
Thomaz, A.T., Arcila, D., Ortí, G. & Malabarba, L.R. (2015): Molecular phylogeny of the subfamily Stevardiinae Gill, 1858 (Characiformes: Characidae): classification and the evolution of reproductive traits. BMC Evolutionary Biology, (2015) 15: 146.
Tectaria is a genus of fern in the family Tectariaceae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). Halberd fern is a common name for species in this genus.
The hindwings are grayish brown., 2006: Phylogeny and life history evolution of Prodoxus yucca moths (Lepidoptera: Prodoxidae). Systematic Entomology 31: 1-20. Adults are on wing from late June to mid August.
ConchBooks, Frankfurt, 360 pp. page(s): 206Johnson R.F. & Gosliner T.M. (2012) Traditional taxonomic groupings mask evolutionary history: A molecular phylogeny and new classification of the chromodorid nudibranchs. PLoS ONE 7(4): e33479.
Leaché, A.D. et al. (2009). Phylogeny of the genus Agama based on mitochondrial DNA sequence data. Bonner zoologische Beiträge 56(4) 273-78.,Mediannikov, O., Trape, S. and Trape, J-F. (2012).
"A redescription of Chaoyangia beishanensis (Aves) and a comprehensive phylogeny of Mesozoic birds." Journal of Systematic Palaeontology, (advance online publication). while some studies continued to find them just outside the yanonrithiform clade.
Simpson, B. B., et al. (2009). Phylogeny and evolution of Perezia (Asteraceae: Mutisieae: Nassauviinae). Journal of Systematics and Evolution 47(5), 431-43. The genus Burkartia was erected for it in 1976.
Jarvis, K., Hass, F., and Whiting, M. 2005. Phylogeny of earwigs based on molecular and morphological evidence. Systematic Entomology, 30, 442-453. L. riparia are a subsocial earwig with complex maternal habits.
Micropolypodium is a genus of ferns in the family Polypodiaceae, subfamily Grammitidoideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). It is native to China, Japan, and the Philippines.
This order consists of Cardiopteridaceae, its sister family, Stemonuraceae, and the three monogeneric families Phyllonomaceae, Helwingiaceae, and Aquifoliaceae.Peter F. Stevens (2001 onwards). "Aquifoliales" At: Angiosperm Phylogeny Website. At: Missouri Botanical Garden Website.
"Higher phylogeny of zygaenid moths (Insecta: Lepidoptera) inferred from nuclear and mitochondrial sequence data and the evolution of larval cuticular cavities for chemical defence." Molecular Phylogenetics and Evolution 39(3): 812-829.
New information on Segisaurus halli, a small theropod dinosaur from the Early Jurassic of Arizona. Journal of Vertebrate Paleontology 25(4): 835-849.Tykoski, 2005. Anatomy, ontogeny and phylogeny of coelophysoid theropods.
The ringed kingfisher is from the family Alcedinidae in the order Coraciiformes.Sibley, C.G. and J.E. Ahlquist (1990). Phylogeny and classification of birds: a study in molecular evolution. New Haven: Yale Univ. Press.
Cladogram of Telluraves relationships based on Prum, R.O. et al. (2015)Prum, R.O. et al. (2015) A comprehensive phylogeny of birds (Aves) using targeted next-generation DNA sequencing. Nature 526, 569–573.
The banded darter is one of the most common darters in North America, where an estimated 250 species of darters occur.Near et al. 2011. Phylogeny and Temporal Diversification of Darters. Systematic Biology.
Molecular phylogeny based on sequences of the SSU rRNA gene suggests that the genus Remanella might be paraphyletic with respect to a monophyletic genus Loxodes but this result is not strongly supported.
Bourne, C.E.M. (1992). Chloroplast DNA structure, variation and phylogeny in closely related species of Cyclotella. ProQuest Dissertations Publishing. The C. meninghiana chloroplast genome alone has a vast amount of equimolar inversion isomers.
Coddington, J. A. (1990). Ontogeny and homology in the male palpus of orb-weaving spiders and their relatives, with comments on phylogeny (Araneoclada: Araneoidea, Deinopoidea). Smithsonian Contributions to Zoology 496: 1-52.
San Diego, Academic Press. In 1977, all but two species were moved into Cantius by Philip D. Gingerich on the basis of differences in their molars.Gebo, DL. 2002. Adapiformes: phylogeny and adaptation.
Zootaxa, 4170(2), 339-354.Agarwal, I., & Karanth, K. P. (2015). A phylogeny of the only ground-dwelling radiation of Cyrtodactylus (Squamata, Gekkonidae): diversification of Geckoella across peninsular India and Sri Lanka.
Kim, H. G., et al. (2003). A phylogeny of the Munnoziinae (Asteraceae, Liabeae): circumscription of Munnozia and a new placement of M. perfoliata. Plant Systematics and Evolution 239(3-4), 171-85.
MacDougall, M.J.; Modesto, S.P.; Brocklehurst,N.; Verriere, A.; Reisz, R.R.; Fröbisch, J. (2018). "Response: A Reassessment of the Taxonomic Position of Mesosaurs, and a Surprising Phylogeny of Early Amniotes". Front. Earth Sci.
Camponotus sansabeanus is a species of ant in the family Formicidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Formica glacialis is a species of ant in the family Formicidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
The fine structure of the parasitic dinoflagellate Haplozoon axiothellae. Protoplasma, 81(1), 17-35. doi: 10.1007/BF02055771 Haplozoon praxillellae,Rueckert, S., & Leander, B. (2008). Morphology and molecular phylogeny of Haplozoon praxillellae n. sp.
Aphaenogaster uinta is a species of ant in the family Formicidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Camponotus sexguttatus is a species of ant in the family Formicidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
"Phylogeny and diversification of the largest avian radiation". Proc. Natl. Acad. Sci. USA. 101: 11040–11045. doi:10.1073/pnas.0401892101. PMC 503738. . some researchers include all these families in a broadly defined Corvidae.
Coptotriche pulverea is a moth of the family Tischeriidae. It was described by Walsingham in 1897.Global diversity; phylogeny of Tischeriidae It is found on the Virgin Islands (St. Thomas) and in Belize.
Molecular phylogeny of the Blastocladiomycota (Fungi) based on nuclear ribosomal DNA. Fungal Biology 115:381-392. This early diverging branch of kingdom Fungi is the first to exhibit alternation of generations.Kendrick, Bryce. 2000.
Megalochoerus is an extinct genus of large and long-legged animals in the pig family from the Miocene of Africa.Pickford, Martin. 1993. Old world suoid systematics, phylogeny, biogeography, and biostratigraphy. Paleontologia i Evolucio.
Journal of Paleontology, 91(3): 554-565. doi:10.1017/jpa.2017.19Starnes, W.C., 1988. "Revision, phylogeny and biogeographic comments on the circumtropical marine percoid fish family Priacanthidae." Bull. Mar. Sci. 43(2):117-203.
Cyclogramma is a genus of ferns in the family Thelypteridaceae, subfamily Thelypteridoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). Other sources sink Cyclogramma into a very broadly defined genus Thelypteris.
Anseriformes is an order of birds belonging to the clade Galloanseres. It consists of 3 families, 58 genera and 171 living species. Extinct species assignment follows the Mikko's Phylogeny Archive and Paleofile.com websites.
The hindwings range from light to medium gray.TOLweb Adults are on wing from April to June., 2006: Phylogeny and life history evolution of Prodoxus yucca moths (Lepidoptera: Prodoxidae). Systematic Entomology 31: 1-20.
Barker G. M.: Gastropods on Land: Phylogeny, Diversity and Adaptive Morphology. in Barker G. M. (ed.): The biology of terrestrial molluscs. CABI Publishing, Oxon, UK, 2001, . 1-146, cited pages: 139 and 142.
A 2019 study presented the first densely sampled molecular phylogeny of Drilini based on nuclear and mitochondrial markers, recovering 5 major clades well supported by morphology along with several new genera and species.
Angiosperm Phylogeny Website At: Missouri Botanical Garden Website. (see External links below). It is now known that Cunoniaceae belongs in Oxalidales.Jason C. Bradford, Helen C. Fortune-Hopkins, and Richard W. Barnes. 2004. "Cunoniaceae".
Annona jamaicensis is a species of plant in the Annonaceae family. It is endemic to Jamaica. Its pollen is shed as permanent tetrads.Walker JW (1971) Pollen Morphology, Phytogeography, and Phylogeny of the Annonaceae.
Desmophlebium is a genus of ferns. In the Pteridophyte Phylogeny Group classification of 2016, it is the only genus in the family Desmophlebiaceae. Other sources place it in a more widely defined Aspleniaceae.
Petalophyllum americanum, common name petalwort, is a species of liverwort in the order Fossombroniales.Crandall-Stotler, B.J., Stotler, R.E., and Long, D.G. 2009. Phylogeny and classification of the Marchantiophyta. Edinburgh Journal of Botany, vol.
Pp. 1-32 in Benton, M. J. (ed), The Phylogeny and Classification of the Tetrapods, Volume 1: Amphibians, Reptiles, Birds. Clarendon Press, Oxford. but some recent analyses suggest that they are stem-tetrapods.
Plocosperma is the sole genus in the Plocospermataceae,Stevens, P.F. (2001 onwards), Plocospermataceae, Angiosperm Phylogeny Website, retrieved 2013-08-15 a family of flowering plants. The genus contains a single species, Plocosperma buxifolium.
Barker G. M.: Gastropods on Land: Phylogeny, Diversity and Adaptive Morphology. in Barker G. M. (ed.): The biology of terrestrial molluscs. CABI Publishing, Oxon, UK, 2001, . 1-146, cited pages: 139 and 142.
The Penaeaceae are a family of evergreen, leathery-leaved shrubs and small trees, native to South Africa. The family has 29 species in 9 genera.Stevens, P. F. (2001 onwards). Penaeaceae.. Angiosperm Phylogeny Website.
The rhynchocephalian genera Homoeosaurus and Pleurosaurus were also found in the formation alongside several turtles such as Eurysternum and Paleomedusa.Dupret, V. (2004). The pleurosaurs: anatomy and phylogeny. Revue de Paléobiologie, 9: 61-80.
The title Persoonia is also given to a biannual scientific journal of molecular phylogeny and evolution of fungi, published jointly by the National Herbarium of the Netherlands and the CBS Fungal Biodiversity Centre.
Both morphological and molecular phylogeny analyses disagree over bryozoans' relationships with entoprocts, about whether bryozoans should be grouped with brachiopods and phoronids in Lophophorata, and whether bryozoans should be considered protostomes or deuterostomes.
Barker G. M.: Gastropods on Land: Phylogeny, Diversity and Adaptive Morphology. in Barker G. M. (ed.): The biology of terrestrial molluscs. CABI Publishing, Oxon, UK, 2001, . 1-146, cited pages: 139 and 142.
The anatomy of conodonts. Philosophical Transactions of the Royal Society of London, Series B 340: 405-421Donoghue, P. C. J., Forey, P. L. and Aldridge, R. J. 2000. Conodont affinity and chordate phylogeny.
Astroloba is a genus of flowering plants in the family Asphodelaceae, subfamily Asphodeloideae,Stevens, P.F. (2001 onwards), "Asphodeloideae", Angiosperm Phylogeny Website, retrieved 2016-06-10 native to the Cape Province of South Africa.
Melpomene is a genus of ferns in the family Polypodiaceae, subfamily Grammitidoideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). It is native to the Neotropical realm in the Americas.
Bloomington: Indiana University Press. Pp. 454–483.Hill, R.V., Witmer, L.M., Norell, M.A. 2003. A New specimen of Pinacosaurus grangeri (Dinosauria: Ornithischia) from the Late Cretaceous of Mongolia: ontogeny and phylogeny of ankylosaurs.
Caesia is a genus of herbs in the family Asphodelaceae, subfamily Hemerocallidoideae,Stevens, P.F. (2001 onwards). "Hemerocallidoideae". Angiosperm Phylogeny Website. Retrieved 2016-06-10. native to Australia, New Guinea, Madagascar and Southern Africa.
C.A. Forster, however, found no evidence of large muscle attachments on the frill bones.Forster, C. A. (1990). The cranial morphology and systematics of Triceratops, with a preliminary analysis of ceratopsian phylogeny. Ph.D. Dissertation.
The molecular phylogeny of Matthiola R. Br.(Brassicaceae) inferred from ITS sequences, with special emphasis on the Macaronesian endemics. Molecular Phylogenetics and Evolution 53(3) 972-81. to 50 speciesMatthiola. Flora of China.
The callus can be highly modified with striking colors that may aid in pollinator deceit and mimicry.Dressler, R.L. 1993. Phylogeny and Classification of the Orchid Family. Portland, Oregon: Dioscorides Press. pp. 29-30.
Goniopteris is a genus of ferns in the family Thelypteridaceae, subfamily Thelypteridoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). Other sources sink Goniopteris into a very broadly defined genus Thelypteris.
Acta Hort 615: Pp. 107-114.Wang, X.-Q., Tank, D. C. and Sang, T. (2000): Phylogeny and Divergence Times in Pinaceae: Evidence from Three Genomes. Molecular Biology and Evolution 17:773-781.
Parathelypteris is a genus of ferns in the family Thelypteridaceae, subfamily Thelypteridoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). Other sources sink Parathelypteris into a very broadly defined genus Thelypteris.
Mannion, P.D.; Upchurch, P.; Jin, X.; Zheng, W. (2019). New information on the Cretaceous sauropod dinosaurs of Zhejiang Province, China: impact on Laurasian titanosauriform phylogeny and biogeography. Royal Society Open Science. 6 (8). .
One of the resolutions to reduce the implications of incomplete lineage sorting is to use multiple genes for creating species or population phylogenies. The more genes used, the more reliable the phylogeny becomes.
Furthermore, unlike Reticulidia fungia, Reticulidia halgerda does not possess a broad bluish white border.Brunckhorst, D.J., 1993, The systematics and phylogeny of Phyllidiid Nudibranchs (Doridoidea). Records of the Australian Museum, Supplement 16: 1-107.
The olfactory component of floral display in Asimina and Deeringothamnus (Annonaceae). New Phytologist 183 457-69. Its pollen is shed as permanent tetrads.Walker JW (1971) Pollen Morphology, Phytogeography, and Phylogeny of the Annonaceae.
S. barbatus eggs, Muséum de Toulouse The phylogeny of this species has been researched by Antonio Arnaiz-Villena et al. Evidence of hybridization was found between Serinus canaria domestica and S.barbatus in captivity.
Cladogram after Mihlbachler (2008):Matthew C. Mihlbachler: Species taxonomy, phylogeny, and biogeography of the Brontotheriidae (Mammalia: Perissodactyla). Bulletin of the American Museum of Natural History 311, 2008, ISSN 0003-0090, S. 1–475.
Harrison, R. G. , S. M. Bogdanowicz , R. S. Hoffmann , E. Yensen , and P. W. Sherman . 2003. Phylogeny and evolutionary history of the ground squirrels (Rodentia: Marmotinae). Journal of Mammalian Evolution 10:249–276.
This article is based on the second circumscription, as presented by the Angiosperm Phylogeny Website. The Malvaceae s.l. (hereafter simply "Malvaceae") comprise nine subfamilies. A tentative cladogram of the family is shown below.
Harrison, R. G. , S. M. Bogdanowicz , R. S. Hoffmann , E. Yensen , and P. W. Sherman . 2003. Phylogeny and evolutionary history of the ground squirrels (Rodentia: Marmotinae). Journal of Mammalian Evolution 10:249–276.
Simplified phylogeny of northwestern branches of Bantu by Grollemund (2012):Grollemund, Rebecca. 2012. Nouvelles approches en classification : Application aux langues bantu du Nord- Ouest. Ph.D Dissertation, Université Lumière Lyon 2, Lyon, 550 pp.
Terpsichore is a genus of ferns in the family Polypodiaceae, subfamily Grammitidoideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). It is native to the Neotropical realm in the Americas.
"Phylogeny and biogeography of Rhododendron subsection Pontica, a group with a Tertiary relict distribution". Molecular Phylogenetics and Evolution 33: 389–401.Kikvidze Z, Ohsawa M. 1999. "Adjara, East Mediterranean refuge of Tertiary vegetation".
The taxonomy of O. trifallax has been contested. It was reclassified as Sterkiella histriomuscorum on the basis of morphological characteristics, but a molecular phylogeny supports the original classification as a species of Oxytricha.
When it was originally described, Diamantinasaurus was assigned to Lithostrotia incertae sedis. In both phylogenies it was placed in, Diamantinasaurus was either just outside Saltasauridae or the sister taxon of Opisthocoelicaudia within the family. In a 2014 study, it was found that the genus was placed as a lithostrotian in both large phylogenies, in a relatively derived position in Titanosauria. Their first phylogeny was modified from that of Carbadillo and Sander (2014), the matrix being indirectly based on Wilson's 2002 phylogeny.
Haplogroup U9 is a rare clade in mtDNA phylogeny, characterized only recently in a few populations of Pakistan (Quintana-Murci et al. 2004). Its presence in Ethiopia and Yemen, together with some Indian-specific M lineages in the Yemeni sample, points to gene flow along the coast of the Arabian Sea. Haplogroups U9 and U4 share two common mutations at the root of their phylogeny. It is interesting that, in Pakistan, U9 occurs frequently only among the so-called Makrani population.
The phylogeny of the dwarf shrew is very controversial. Given the sheer number of species in the genus Sorex, they are difficult to tell apart. A phylogeny is proposed, and widely accepted now, in which S. vagrans gave rise to S. nanus along with S. longirostris and S. ornatus. This same theory provides evidence that S. nanus and S. tenellus diverged more recently than their relatives because they are morphologically indistinguishable from each other except for very small size differences.
A phylogeny of the Papilionidae based on Nazari (2007) is given: It is now accepted that the subfamily Papilioninae is monophyletic. The swallowtail butterflies in the nominate tribe Papilionini number about 225 species and studies have been made on their host plant coevolution and phylogeny. Old morphological classifications were also found to be valid in that they formed clusters. Species belonging to the groups that use Rutaceae as host plants formed two groups corresponding to Old World and American taxa.
Annals of the Missouri Botanical Garden 80(3):528-580. The phylogeny produced by this study placed Lepuropetalon and Parnassia together, but only four members of Celastrales were sampled and the authors could not calculate statistical support for their clades. In 2000, an rbcL phylogeny of eudicots again put Lepuropetalon and Parnassia together, but with only weak statistical support. In 2001, in a study that used much more DNA, Lepuropetalon again grouped with Parnassia, but with strong statistical support (98% bootstrap percentage).
A study of the molecular phylogeny of the subtribe Eulophiinae published in 2014 considered that this species was more closely allied with the genus Oeceoclades, but the move has not been accepted by the World Checklist of Selected Plant Families and the name Oeceoclades pulchra is regarded as a synonym.Martos, F., S. D. Johnson, C. I. Peter, and B. Bytebier. 2014. A molecular phylogeny reveals paraphyly of the large genus Eulophia (Orchidaceae): A case for the reinstatement of Orthochilus. Taxon 63: 9-23.
Benson attributed this revised phylogeny to the inclusion of postcranial characteristics, or features of the skeleton other than the skull, in his analysis. When only cranial or skull features were included, Caseasauria remained the most basal synapsid clade. Below is a cladogram modified from the analysis of Benson (2012): However, more recent examination of the phylogeny of basal synapsids, incorporating newly described basal caseids and eothyridids, returned Caseasauria to its position as the sister to all other synapsids. Brocklehurst et al.
This reassignment has yet to enjoy universal acceptance, but is gaining in popularity among taxonomists working with these fishes. Given the current state of flux of the Characidae, a number of other changes will doubtless take place, reassigning once-familiar species to other families. Indeed, the entire phylogeny of the Ostariophysi – fishes possessing a Weberian apparatus – has yet to be settled conclusively. Until that phylogeny is settled, the opportunity for yet more upheavals within the taxonomy of the characoid fishes is considerable.
Recent phylogenetic analyses has place Varanopidae as a basal member of Synapsida and due to their positioning, a better understanding of the morphology and phylogeny of varanopids is needed for synapsid evolution. The phylogeny of varanopids should be based mostly on cranial morphology. The atlas−axis complex can be described with little effort with variation of this structure within a small clade. Varanopids, members of synapsid predators have well preserved atlas−axes permitting a descriptions and examination of morphological variation between taxon.
Asparagales (asparagoid lilies) is an order of plants in modern classification systems such as the Angiosperm Phylogeny Group (APG) and the Angiosperm Phylogeny Web. The order takes its name from the type family Asparagaceae and is placed in the monocots amongst the lilioid monocots. The order has only recently been recognized in classification systems. It was first put forward by Huber in 1977 and later taken up in the Dahlgren system of 1985 and then the APG in 1998, 2003 and 2009.
Wüster W, Peppin L, Pook CE, Walker DE. 2008. A nesting of vipers: phylogeny and historical biogeography of the Viperidae (Squamata: Serpentes). Molecular Phylogenetics and Evolution 49: 445-459. Seven species are currently recognized.
Lasioglossum pilosum is a species of sweat bees in the family Halictidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Pessopteryx is an extinct genus of ichthyosaur from the Early Triassic (Olenekian) of Svalbard, Norway.M. W. Maisch. 2010. Phylogeny, systematics, and origin of the Ichthyosauria - the state of the art. Palaeodiversity 3:151-214.
Manica hunteri is a species of ant in the family Formicidae. Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera. "Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Chrysis provancheri is a species of cuckoo wasp in the family Chrysididae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Lasioglossum petrellum is a species of sweat bee in the family Halictidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Sphecodes davisii is a species of sweat bee in the family Halictidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Scolia nobilitata is a species of scoliid wasp in the family Scoliidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Auplopus mellipes is a species of spider wasp in the family Pompilidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Tromatobia ovivora is a species of ichneumon wasp in the family Ichneumonidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Taxonus terminalis is a species of common sawfly in the family Tenthredinidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
American Zoologist 41:564–585.Delfino, M., Piras, P., and Smith, T. (2005). Anatomy and phylogeny of the gavialoid crocodylian Eosuchus lerichei from the Paleocene of Europe. Acta Palaeontologica Polonica 50(3):565–580.
Coptotriche forsteroniae is a moth of the family Tischeriidae. It was described by Stonis and Diškus in 2008.Global diversity; phylogeny of Tischeriidae It is found in Belize. The larvae feed on Forsteronia myriantha.
Coptotriche roseticola is a moth of the family Tischeriidae. It was described by Frey and Boll in 1873.Global diversity; phylogeny of Tischeriidae It is found in Ohio. The larvae feed on Rosa setigera.
The forewings are white with a chocolate brown area. The hindwings are white with light gray shading., 2006: Phylogeny and life history evolution of Prodoxus yucca moths (Lepidoptera: Prodoxidae). Systematic Entomology 31: 1-20.
The hindwings are white with a light gray apex., 2006: Phylogeny and life history evolution of Prodoxus yucca moths (Lepidoptera: Prodoxidae). Systematic Entomology 31: 1-20. Adults are on wing from March to April.
PDF . has raised the tribe Eocypraeini to the status of the family Eocypraeidae, based on morphological research of the radulae, shell and animal morphology and molecular phylogeny research of the 16S ribosomal RNA gene.
Senter, P. (2004). "Phylogeny of Drepanosauridae (Reptilia: Diapsida)." Journal of Systematic Palaeontology, 2(3): 257-268. The tail of this genus was extremely deep and non-prehensile – much more fin-like than other drepanosaurs.
Its closest relative is Sphenostemon.Tank, D. C., and M. J. Donoghue. (2010). Phylogeny and Phylogenetic Nomenclature of the Campanulidae Based on an Expanded Sample of Genes and Taxa. Systematic Botany 35 (2): 425–41.
Rudman W.B. & Darvell B.W. (1990) Opisthobranch molluscs of Hong Kong: Part 1. Goniodorididae, Onchidorididae, Triophidae, Gymnodorididae, Chromodorididae (Nudibranchia). Asian Marine Biology 7: 31-79. page(s): 54 This clade is supported by molecular phylogeny.
There is a genetic proposal to reassign this species to the genus Protobothrops, as Protobothrops xiangchengensis, because a "phylogeny of four mitochondrial gene regions suggests a revised taxonomy for Asian pitvipers (Trimeresurus and Ovophis)".
Molecular phylogeny and taxonomic revision of Chlamydomonas (Chlorophyta). I. Emendation of Chlamydomonas Ehrenberg and Chloromonas Gobi, and descripription of Oogamochlamys gen. nov. and Lobochlamys gen. nov. Protist 152: 265-300, 7 figs, 5 tables, .
Susy Fuentes-Bazan, Pertti Uotila, Thomas Borsch: A novel phylogeny-based generic classification for Chenopodium sensu lato, and a tribal rearrangement of Chenopodioideae (Chenopodiaceae). In: Willdenowia. Vol. 42, No. 1, 2012, p. 15-16.
The Eublepharidae are a family of geckos (Gekkota) consisting of 30 described species in six genera. They occur in Asia, Africa and North America.Grismer, L.L. 1988. Phylogeny, taxonomy, classification, and biogeography of eublepharid geckos.
Johns Hopkins University Press, Baltimore. Witmer, L. (2002). "The debate on avian ancestry: phylogeny, function, and fossils." Pp. 3-30 in: Chiappe, L.M. and Witmer, L.M. (eds), Mesozoic birds: Above the heads of dinosaurs.
DaCosta, M. A. (2010). Phylogeny of Utetheisa s. str.(Lepidoptera: Noctuidae: Arctinae) with comments on the evolution of colour, hind wing scales and origin of New World species. Invertebrate Systematics 24(2), 113-30.
Phylogeny and paraphyly among tetrapod blood flukes (Digenea: Schistosomatidae and Spirorchiidae). International Journal for Parasitology 34(12), 1385-92. It has been synonymised with Proparorchiidae Ward, 1921, Spirorchidae Stunkard, 1921, and Spirorchiidae MacCallum, 1921.
Trichoneuron is a genus of ferns in the family Dryopteridaceae, subfamily Polybotryoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). The genus has a single species Trichoneuron microlepioides, native to Yunnan, China.
The precise limits between Arctium and Cousinia are hard to define; there is an exact correlation between their molecular phylogeny. The burdocks are sometimes confused with the cockleburs (genus Xanthium) and rhubarb (genus Rheum).
Amauropelta is a genus of ferns in the family Thelypteridaceae, subfamily Thelypteridoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). Other sources sink the genus into a very broadly defined genus Thelypteris.
Though its relationships to other members of this group are inadequately known, Pasquiaornis appears to have been one of the more basal lineages. (2004): The Theropod Database: Phylogeny of taxa . Retrieved 2013-MAR-02.
The evolution and ecology of armadillos, sloths, and vermilinguas. Smithsonian Institution Press, Washington, DC, 51-64.Wible, J. R. (2006). 6 The Phylogeny of Living and Extinct Armadillos (Mammalia, Xenarthra, Cingulata): A Craniodental Analysis.
This species was first collected in Mauritius. It was confused with Phyllidiella annulata by Brunckhorst.Brunckhorst, D.J. (1993) The systematics and phylogeny of Phyllidiid Nudibranchs (Doridoidea). Records of the Australian Museum, Supplement 16: 1-107.
50 million years, so its original function must be different from its current one.Yager, D. D. & Svenson, G. J. (2008). "A phylogeny of mantis auditory systems based on morphological, molecular, physiological, and behavioral data".
Phylogeny of early Tertiary swifts and hummingbirds (Aves: Apodiformes). Auk, 120 (1): 145-151.Mayr, G. (2010). Reappraisal of Eocypselus – a stem group representative of apodiform birds from the early Eocene of Northern Europe.
These insects are known commonly as cochineals,Ramírez-Puebla, S. T., et al. (2010). Molecular phylogeny of the genus Dactylopius (Hemiptera: Dactylopiidae) and identification of the symbiotic bacteria. Environmental Entomology 39(4), 1178-83.
Weems, R. E. 1988. Paleocene turtles from the Aquia and Brightseat formations, with a discussion of their bearing on sea turtle evolution and phylogeny. Proceedings of the Biological Society of Washington 101:109–145.
Klaver CJ, Böhme W (1986). "Phylogeny and classification of the Chamaeleonidae (Sauria) with special reference to hemipenis morphology". Bonner Zoologische Monographien 22: 1–64.Tolley, Krystal A.; Tilbury, Colin R.; Branch, William R. (2004).
In terms of phylogeny, this species is very isolated. I has no clear relationships to any other member of the genus Anodonthyla. It has a genetic 16S divergence of 9.4-12.1% relative to other species.
Isodontia exornata is a species of thread-waisted wasp in the family Sphecidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Sensu Schrödl & Neusser (2010)Schrödl M. & Neusser T. P. (2010). "Towards a phylogeny and evolution of Acochlidia (Mollusca: Gastropoda: Opisthobranchia)". Zoological Journal of the Linnean Society 158: 124-154. . is Microhedylidae within the clade Microhedylacea.
New York: Bulletin of the American Museum of Natural History, 1953. Print.Prum, R. O. (1993). Phylogeny, biogeography, and evolution of the broadbills (Eurylaimidae) and asities (Philepittidae) based on morphology. The Auk 110(2) 304-24.
It reaches 15 to 20 meters tall. Its pollen is shed as permanent tetrads.Walker JW (1971) Pollen Morphology, Phytogeography, and Phylogeny of the Annonaceae. Contributions from the Gray Herbarium of Harvard University, 202: 1-130.
PDF . raised the subfamily Pediculariinae to the level of family as Pediculariidae, based on morphological research on the radulae, the shell, the soft part morphology and molecular phylogeny research on the 16S ribosomal RNA gene.
Their systematic and phylogeny. Akad. Nauka. USSR. English translation by the American Institute of Biological Science, Washington. 509 pp Yamaguti (1963),Yamaguti, S. (1963) Systema Helminthum IV. Monogenea and Aspidocotylea. London-New York, Interscience Publishers.
Its pollen is shed as permanent tetrads.Walker JW (1971) Pollen Morphology, Phytogeography, and Phylogeny of the Annonaceae. Contributions from the Gray Herbarium of Harvard University, 202: 1-130. The fruits are dark green and prickly.
Stephanie M. Ickert-Bond and Jun Wen. 2006. "Phylogeny and biogeography of Altingiaceae: Evidence from combined analysis of five non-coding chloroplast regions". Molecular Phylogenetics and Evolution 39(2):512-528. (see External links below).
Pardo and Mann (2018) demonstrated that H. longidentatum belongs to the limbless tetrapod clade Aistopoda and renamed it Andersonerpeton in honor of Jason S. Anderson, a contributor to enhanced understanding of aïstopod morphology and phylogeny.
The following phylogeny of Tylototriton is from Nishikawa, Matsui & Rao (2014).Nishikawa, Matsui & Rao, 2014 : A new species of Tylototriton (Amphibia: Urodela: Salamandridae) from central Myanmar. Natural History Bulletin of the Siam Society, , no. 1, .
These results are due to correlation between the vast differences in diet coupled with large and adaptive differences in beak morphology. However, with similar levels of Finch phylogeny showed ongoing divergence, diet overlap and competition.
Then the subfamily Sycophaginae have been placed within the family Agaonidae. Within the Sycophaginae, some changes were made after the molecular phylogeny of the subfamily: the genus Apocryptophagus has been synonymined under the genus Sycophaga.
Dinapoli A, Zinssmeister C, Klussman-Kolb A. 2011. New insights into the phylogeny of the Pyramidellidae (Gastropoda). Journal of Molluscan Studies 77:1-7. The family is currently divided into 11 subfamilies (Ponder & Lindberg 1997).
Nancy F. Refulio-Rodriguez and Richard G. Olmstead. 2014. "Phylogeny of Lamiidae". American Journal of Botany 101(2):287-299. Two of these families, Mazaceae and Rehmanniaceae are not part of the APG III system.
Phrymaceae, also known as the lopseed family, is a small family of flowering plants in the order Lamiales.Peter F. Stevens (2001 onwards). "Phrymaceae" At: Angiosperm Phylogeny Website. At: Botanical Databases At: Missouri Botanical Garden Website.
Megalastrum is a genus of ferns in the family Dryopteridaceae, subfamily Elaphoglossoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). The genus has around 100 species, mainly found in tropical America and Africa.
Springer-Verlag: Berlin;Heidelberg, Germany. Perrottetia, meanwhile, had usually been placed, with considerable doubt, in Celastraceae.Li-Bing Zhang and Mark P. Simmons (2006). "Phylogeny and Delimitation of the Celastrales Inferred from Nuclear and Plastid Genes".
Phylogeny and generic interrelationships of the Stylidiaceae (Asterales), with a possible extreme case of floral paedomorphosis. Systematic Botany, 23(3): 289-304.Wagstaff, S.J. and Wege, J. (2002). Patterns of diversification in New Zealand Stylidiaceae.
Banded blennies are small and slender. Their standard length is 15 mm.[Pazmandi, C. (2000) Blenniid phylogeny and the evolution of the fin hook characters (Order No. 9973753). Available from ProQuest Dissertations & Theses Global. (304646100)].
Ctenopterella is a genus of ferns in the family Polypodiaceae, subfamily Grammitidoideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). It is known from Africa through southeast Asia and Oceania to Polynesia.
An early cladistic analysis of crocodylotarsan archosaurs included Poposaurus, Postosuchus, Teratosaurus, and Bromsgroveia within Poposauridae.Parrish JM. 1993. Phylogeny of the Crocodylotarsi, with reference to archosaurian and crurotarsan monophyly. Journal of Vertebrate Paleontology 13: 287-308.
"Evolution of a Charismatic Neotropical Clade: Molecular Phylogeny of Tabebuia s.l., Crescentieae, and Allied Genera (Bignoniaceae)". Systematic Botany 32(3):650-659. It is commonly cultivated and often naturalized or adventive beyond its natural range.
Phylogeny of the Notoungulata (Mammalia) based on cranial and dental characters. Journal of Systematic Palaeontology 9: 481–497. although this is still a controversial idea. Cladogram based on the phylogenetic analysis of Cerdeño et al.
Acrosorus is a genus of ferns in the family Polypodiaceae, subfamily Grammitidoideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). It is known from the Philippines, Malesia, Thailand, and the Pacific islands.
WoolleyWoolley, J. B. (1988). Phylogeny and classification of the Signiphoridae (Hymenoptera: Chalcidoidea). Systematic Entomology 13:465-501. made several changes in the classification at genus and species level after a phylogenetic analysis of the family.
Phylogeny of early Tertiary Carnivora, with a description of a new species of Protictis from the middle Eocene of northwestern Wyoming. American Museum NovitatesH. N. Bryant. 1991. Phylogenetic relationships and systematics of the Nimravidae (Carnivora).
Johns, C. A., Moore, M. R., & Kawahara, A. Y. (2016). Molecular Phylogeny, Revised Higher Classification, and Implications for Conservation of Endangered Hawaiian Leaf-Mining Moths (Lepidoptera: Gracillariidae: Philodoria) 1. Pacific Science, 70(3), 361-372.
Stegnogramma is a genus of ferns in the subfamily Thelypteridoideae of the family Thelypteridaceae in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). Other sources sink Stegnogramma into a very broadly defined genus Thelypteris.
Plenasium is a genus of ferns in the family Osmundaceae. It is recognized in the Pteridophyte Phylogeny Group classification of 2016 (PPG I), but kept within a more broadly circumscribed genus Osmunda by other sources.
Byttneria is a genus of flowering plants in the family Malvaceae. There are about 135 species in this pantropical genus.Whitlock, B. A., & Hale, A. M. (2011). The phylogeny of Ayenia, Byttneria, and Rayleya (Malvaceae s.
Molecular phylogeny showed however that it belongs in its own clade, the Neomphalina, and that this clade is basal to the Vetigastropoda.Ponder W. F. & Lindberg D. R. (1997). Zool. J. Linn. Soc. 119: 83–265.
It is not known to which of the other families in the order it is most closely related.Peter F. Stevens (2001 onwards). "Bignoniaceae" At: Angiosperm Phylogeny Website. At: Botanical Databases At: Missouri Botanical Garden Website.
Origin and phylogeny has been obtained by Antonio Arnaiz-Villena et al.. Estrildinae may have originated in India and dispersed thereafter (towards Africa and Pacific Ocean habitats). Its closest relative is the red-headed finch.
Ciugulea, Ionel; Nudelman, María A.; Brosnan, Stacy; Triemer, Richard E. (2008). “Phylogeny of the euglenoid loricate genera Trachelomonas and Strombomonas (Euglenophyta) inferred from nuclear SSU and LSU rDNA”. Journal of Phycology. 44 (2): 406-418.
The study by Mockett et al. confirmed that the New Zealand gecko nematodes all belonged to the same genus, Skrjabinodon. Host phylogeny was found to significantly predict the parasite phylogeny, which indicates that cospeciation may have played a role in the evolution of New Zealand geckos and the associated Skrjabinodon, although it was acknowledged that host-switching to closely related host species would have played an important role. It was also noted that “not all host–parasite associations supported a congruent host–parasite phylogenetic history”.
The evolutionary history of the species—which describes the characteristics of the various species from which it descended—together with its genealogical relationship to every other species is known as its phylogeny. Widely varied approaches to biology generate information about phylogeny. These include the comparisons of DNA sequences, a product of molecular biology (more particularly genomics), and comparisons of fossils or other records of ancient organisms, a product of paleontology. Biologists organize and analyze evolutionary relationships through various methods, including phylogenetics, phenetics, and cladistics.
Recently, Dinilysia has been labeled a sister group of all living alethinophidia. Therefore this Crataceous snake still contributes a significant amount within the debate on the origin of snakes and phylogeny. In terms of the locality and age of the Dinilysia the fossils can typically be found in abundance in sandstone sediments favored to the Anacleto formation. Additionally, the overall morphological similarities between that of D. patagonica has been used to determine the phylogeny and possible relations of the characteristics which other more present snakes may share.
Violaceae is a family of flowering plants established in 1802, consisting of about 1000 species in about 25 genera. It takes its name from the genus Viola, the violets and pansies. Older classifications such as the Cronquist system placed the Violaceae in an order named after it, the Violales or the Parietales. However, molecular phylogeny studies place the family in the Malpighiales as reflected in the Angiosperm Phylogeny Group (APG) classification, with 41 other families, where it is situated in the parietal clade of 11 families.
Currently, no cultured isolates of CAP exist, so the phylogeny of CAP strains is based purely of molecular biology techniques. To date, the polyphosphate kinase (ppk1) and the PHA synthase (phaC) genes have been used to characterise CAP populations at a higher resolution that 16S rRNA. The ppk1 phylogeny is more frequently used and groups CAP into two major divisions: type I and type II. Each of these types has a number of clades that are given a letter designation, e.g. IA, IIA, IIB, IIC.
The phylogeny of S. muelleri has been discovered to follow the phylogeny of the Hemiptera clade, Auchenorrhyncha. The first association between S. muelleri and Auchenorrhyncha is estimated to have occurred sometime between 260–280 million years ago. Further evidence supports the idea that S. muelleri has coevolved with another symbiotic lineage from the taxonomic class Betaproteobacteria. The result of this coevolution can be noticed through the fact that both S. muelleri and its host leave cofactor and vitamin production to another member of the symbiotic relationship.
Peter Francis Stevens is a British botanist born in 1944. He is a researcher at the Missouri Botanical Garden and professor of Biology of the University of Missouri–St. Louis. He is a member of the Angiosperm Phylogeny Group which created the APG, APG II, APG III, and APG IV systems. He maintains a web site, APweb, hosted by the Missouri Botanical Garden, which has been regularly updated since 2001, and is a useful source for the latest research in angiosperm phylogeny which follows the APG approach.
If only one-way edges were sufficient to explain the presence of all the states in a language, then there was no need to look beyond the perfect phylogeny. If not, then one or more contact edges, or bidirectional interfaces, could be added to the phylogeny. A language therefore might have more than one source of states: the parent or a contact language. A tree so modified was no longer a tree as such: there could be more than one path from root to leaf.
Modern systematics aims to reflect and discover phylogenetic relationships between plants. Modern Molecular phylogenetics largely ignores morphological characters, relying on DNA sequences as data. Molecular analysis of DNA sequences from most families of flowering plants enabled the Angiosperm Phylogeny Group to publish in 1998 a phylogeny of flowering plants, answering many of the questions about relationships among angiosperm families and species. The theoretical possibility of a practical method for identification of plant species and commercial varieties by DNA barcoding is the subject of active current research.
Marco Duretto (born 1964) is a manager and senior research scientist at the Royal Botanic Gardens Sydney in Australia. His primary research interests are systematics and conservation of Rutaceae, Rubiaceae, Orchidaceae, Stylidiaceae and evolution of Australasian flora. Duretto's projects have included "Phylogeny and biogeography of Boronia (Rutaceae)", "Mutual pollination system involving Boronia (Rutaceae) and moths of the Heliozelidae", "A molecular and morphological phylogeny of the Phebalium Group (Rutaceae)", and "East coast species limits in Stylidium". Marco Duretto was previously a research scientist with the University of Tasmania.
The Cuscutaceae family is closely related to the Oncothecaceae family on an Angiosperm Phylogeny. C. compacta is in the Cleistogrammica section subsection Lepidanche. Two closest species related to C. compacta are, Cuscuta glomerata and Cuscuta denticulata.
Cephalomanes is a fern genus in the family Hymenophyllaceae. The genus is accepted in the Pteridophyte Phylogeny Group classification of 2016 (PPG I) but not by other sources, which sink it into a broadly defined Trichomanes.
A multi-gene phylogeny of aquiline eagles (Aves: Accipitriformes) reveals extensive paraphyly at the genus level. Molecular Phylogenetics and Evolution 35(1):147-164.Haring, E., Kvaløy, K., Gjershaug, J. O., Røv, N., & Gamauf, A. (2007).
Colletes thoracicus, the rufous-chested cellophane bee, is a species of cellophane or plasterer, masked, or fork-tongued bee in the family Colletidae. It is found in North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Euodynerus foraminatus is a species of potter or mason wasp in the family Vespidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Pheidole metallescens is an ant, a species of higher myrmicine in the family Formicidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Erwin et al. (2011) The Cambrian Conundrum: Early Divergence and Later Ecological Success in the Early History of Animals. Science 334: 1091-1097. Phylogeny is based on a combination of studies of extinct and extant species.
According to Schrödl & Neusser (2010)Schrödl M. & Neusser T. P. (2010). "Towards a phylogeny and evolution of Acochlidia (Mollusca: Gastropoda: Opisthobranchia)". Zoological Journal of the Linnean Society 158: 124-154. . Strubellia is in the family Acochlidiidae.
The hindwings are white with a grey area along the front edge., 2006: Phylogeny and life history evolution of Prodoxus yucca moths (Lepidoptera: Prodoxidae). Systematic Entomology 31: 1-20. Adults are on wing in late April.
Oleaceae is most closely related to the small Indo-Malesian family Carlemanniaceae. These two families form the second most basal clade in the order Lamiales, after Plocospermataceae.Peter F. Stevens (2001 onwards). "Oleaceae" At: Angiosperm Phylogeny Website.
Genus-level taxonomic changes implied b mitochondrial phylogeny of grey mullets (Teleostei: Mugilidae). Comptes Rendus Biologies, 335: 687-697. The sand grey mullet fish is part of the family mugilidae that are ray-finned fish (actinopterygii).
Martos, F., S.D. Johnson, C.I. Peter, and B. Bytebier. 2014. A molecular phylogeny reveals paraphyly of the large genus Eulophia (Orchidaceae): A case for the reinstatement of Orthochilus. Taxon 63(1): 9-23.Richard, A. 1850.
The phylogeny below is based on the work of Hughes & Baker 1999 and Mayr & De Pietri 2014. Traditionally classified among the fowl-like birds (Galliformes), recent studies have favored Opisthocomidae's placement with the cuckoos (Cuculiformes: Cuculidae).
"Phylogeny and evolution of grammitid ferns (Grammitidaceae): a case of rampant morphological homoplasy". Taxon 53(2):415-428. They are sister to a clade of 26 species which at that time were in the genus Terpsichore.
Some writers preferring phylogenetic nomenclature use Anthracosauria.Gauthier, J., Kluge, A.G., & Rowe, T. (1988): "The early evolution of the Amniota". In The Phylogeny and Classification of the Tetrapods: Volume 1: Amphibians, Reptiles, Birds. Edited by M.J. Benton.
Molecular phylogeny research by Kraus et al. (2010) based on a part of "intron 9" of the gamma-glutamyl carboxylase gene has shown that feeding on fish has evolved at least twice independently in the group.
The phylogeny of the genera of Rhinantheae has been explored using molecular characters. Bartsia belongs to the core Rhinantheae. Bartsia sensu stricto (e.g. B. alpina) is the sister genus to Odontites, Bellardia, Tozzia, Hedbergia, and Euphrasia.
"Changing Distribution Patterns Of Northern Hemisphere Eudicot Hosts Of Ectoedemia Ss During The Tertiary In Relation To Their Phylogeny: Setting The Scene For Leafminer Evolution." (2009). The larvae are pale green and the cocoon is ochraceous.
Leipzig: Wilhelm Engelmann. The genus was described by Dendy & Row in 1913.Dendy, A. & Row, R. (1913). The classification and phylogeny of the calcareous sponges, with a reference list of all the described species, systematically arranged.
The archaeal single-chain histones are also found in the bacterium Aquifex aeolicus. Which helps the diverse bacteria phylogeny coming from the ancestry of eukaryotes and archaea with lateral gene transfers to get to the bacteria.
"Phylogeny of Lamiidae". American Journal of Botany 101(2):287-299. . The authors of that study believe that Gelsemiaceae should be expanded to include Pteleocarpa. The APG IV system published in 2016 includes Pteleocarpa in Gelsemiaceae.
Phylogeny of Pertusariales (Ascomycotina): Resurrection of Ochrolechiaceae and new circumscription of Megasporaceae. Journal of the Hattori Botanical Laboratory. 100:753-64. The genus Aspicilia was moved here from the Hymeneliaceae.Lumbsch TH, Feige GB, Schmitz KE. (1994).
A multi-gene phylogeny of aquiline eagles (Aves: Accipitriformes) reveals extensive paraphyly at the genus level. Molecular Phylogenetics and Evolution 35(1):147-164.Haring, E., Kvaløy, K., Gjershaug, J. O., Røv, N., & Gamauf, A. (2007).
M. acidophila is part of a clade that contains M. longespiculosa, M. ansisomorpha and two as yet unidentified species of Mesorhabditis (grey box). A phylogenetic tree shows more detailed information about the phylogeny of this species.
A genetic analysis from 1997 suggested that the two were sister taxa.Trewick SA. 1997. Flightlessness and phylogeny amongst endemic rails (Aves: Rallidae) of the New Zealand region. Philosophical Transactions of the Royal Society. 352:429–446.
Polyura is a subgenus of butterflies also referred to as Nawab butterfliesBillberg, 1820; Enum. Ins. Mus. Billb. : 79Smiles, R. L. (1982). The taxonomy and phylogeny of the genus Polyura Billberg (Lepidoptera: Nymphalidae). British Museum (Natural History).
An updated phylogeny and classification of Lamiaceae subfamily Lamioideae. Taxon 60: 471-484. The genus is closely related to Galeobdolon, and the species below are discussed under that name in Flora of China.Flora of China Vol.
"New mosasaur material from the Maastrichtian of Angola, with notes on the phylogeny, distribution and palaeoecology of the genus Prognathodon." On Maastricht Mosasaurs. Publicaties van het Natuurhistorisch Genootschap in Limburg 45.1 (2006): 57-67. Lindgren, Johan.
The tree below is an excerpt from the Rautenbach (2002) phylogeny. The species of Gnidia were chosen from among the most common or well known species in a way that shows which clades contain species of Gnidia.
National Museums of Canada. A recent phylogeny suggests the squirrels as a family can be divided into five major lineages. Red squirrels (Tamiasciurus) fall within the clade that includes flying squirrels and other tree squirrels (e.g., Sciurus).
Lasioglossum tuolumnense, the Tuolumne dialictu, is a species of sweat bee in the family Halictidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
However other authorities including the Angiosperm Phylogeny Website (APWeb) define Lilioideae s.l. to also include the Medeoleae (while subsuming the Tulipae into Lilieae). In the s.s. usage, the Medeoleae are treated as a separate subfamily, the Medeoloideae.
This genus was treated within family Buccinidae. It was moved to family Nassariidae in 2016.Galindo, L. A., Puillandre, N., Utge, J., Lozouet, P., & Bouchet, P. (2016). "The phylogeny and systematics of the Nassariidae revisited (Gastropoda, Buccinoidea)".
This genus was treated within family Buccinidae. It was moved to family Nassariidae in 2016.Galindo, L. A., Puillandre, N., Utge, J., Lozouet, P., & Bouchet, P. (2016). "The phylogeny and systematics of the Nassariidae revisited (Gastropoda, Buccinoidea)".
This genus was treated within family Buccinidae. It was moved to family Nassariidae in 2016.Galindo, L. A., Puillandre, N., Utge, J., Lozouet, P., & Bouchet, P. (2016). "The phylogeny and systematics of the Nassariidae revisited (Gastropoda, Buccinoidea)".
This genus was treated within family Buccinidae. It was moved to family Nassariidae in 2016.Galindo, L. A., Puillandre, N., Utge, J., Lozouet, P., & Bouchet, P. (2016). "The phylogeny and systematics of the Nassariidae revisited (Gastropoda, Buccinoidea)".
Creodonta is an extinct, possibly polyphyleticMorlo, M., Gunnell G., and P.D. Polly. 2009. What, if not nothing, is a creodont? Phylogeny and classification of Hyaenodontida and other former creodonts. Journal of Vertebrate Paleontology 29(Supplement 3): 152A.
In the Pteridophyte Phylogeny Group classification of 2016 (PPG I), Lycopodiella is placed in the subfamily Lycopodielloideae, along with three other genera (Lateristachys, Palhinhaea and Pseudolycopodiella). Other sources do not recognize these genera, submerging them into Lycopodiella.
Hyman's Comparative Vertebrate Anatomy. Chicago: University of Chicago Press, page 39. The evolution of these wing characteristics has provided the hummingbird with ideal wings for hovering.Mayr, Gerald (2003): Phylogeny of early tertiary swifts and hummingbirds (Aves: Apodiformes).
Abrodictyum is a fern genus in the family Hymenophyllaceae. The genus is accepted in the Pteridophyte Phylogeny Group classification of 2016 (PPG I) but not by some other sources, which sink it into a broadly defined Trichomanes.
Callistopteris is a fern genus in the family Hymenophyllaceae. The genus is accepted in the Pteridophyte Phylogeny Group classification of 2016 (PPG I) but not by some other sources, which sink it into a broadly defined Trichomanes.
"A new azhdarchoid pterosaur from the Lower Cretaceous of China and its implications for pterosaur phylogeny and evolution." Naturwissenschaften A redescription of the genus in 2017 corroborated these results, and also presented evidence distinguishing it from Chaoyangopterus.
Since the phylogeny was published, Omphalotus flagelliformis has been described from Yunnan Province in China, which is related to O. mexicanus and O. illudens. The generic name Omphalotus is derived from the Byzantine Greek ὀμϕαλοειδής, meaning "navel".
Chleuastochoerus is an extinct genus in the pig family that lived in the Miocene and PliocenePickford, M. 1993. Old World suoid systematics, phylogeny, biogeography, and biostratigraphy. Paleont. Evol., 26-27:237-269 in Russia and Eastern Asia.
Harvard Papers in Botany, 6(2), 459-480., accessed 08.14.2013.APG III VASCULAR PLANT FAMILIES and GENERA: List of Genera in ADOXACEAE, Angiosperm Phylogeny Group places Viburnum within Adoxaceae, accessed 08.14.2013. It is endemic to eastern Mexico.
The hindwings are gray, but darker along the outer edge., 2006: Phylogeny and life history evolution of Prodoxus yucca moths (Lepidoptera: Prodoxidae). Systematic Entomology 31: 1-20. Adults are on wing from late February to early March.
Simone (2004)Simone L. R. L. (2004). "Morphology and Phylogeny of the Cypraeoidea (Mollusca, Caenogastropoda)". Papel Virtual Editoria (Rio de Janeiro): 185 pp. placed some genera in the family Pediculariidae which were previously in the family Ovulidae.
Angiosperm Phylogeny Website In: Missouri Botanical Garden Website. (see External links below). and about 350,000 that are. While such a clade with a similar circumscription exists in the APG III system, it was not given a name.
Of about 75 species, 71 can be found in South Africa.Funk, V. A. and R. Chan. (2008). Phylogeny of the spiny African daisies (Compositae, tribe Arctotideae, subtribe Gorteriinae) based on trnL-F, ndhF, and ITS sequence data.
Jaltomata is a genus of plants in the family Solanaceae. According to molecular phylogenies, Jaltomata is the sister genus to Solanum, which includes tomato, potato, and eggplant.Olmstead, RW et al. 2008. A molecular phylogeny of the Solanaceae.
Essai de phylogenèse. Thèse d'État, Académie de Montpellier, Université des Sciences et Techniques du Languedoc, France. According to the classical book of Bychowsky (1967),Bychowsky, B. E. (1957) Monogenetic Trematodes. Their systematic and phylogeny. Akad. Nauka. USSR.
This genus was treated within family Buccinidae. It was moved to family Nassariidae in 2016.Galindo, L. A., Puillandre, N., Utge, J., Lozouet, P., & Bouchet, P. (2016). "The phylogeny and systematics of the Nassariidae revisited (Gastropoda, Buccinoidea)".
Calymmodon is a genus of ferns in the family Polypodiaceae, subfamily Grammitidoideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). Its known range is Sri Lanka, Thailand, Vietnam, Taiwan, Malesia, Australia, Micronesia and Polynesia.
Oskars, T. R. and M. A. E. Malaquias. 2019. A molecular phylogeny of the Indo-West Pacific species of Haloa sensu lato gastropods (Cephalaspidea: Haminoeidae): Tethyan vicariance, generic diversity, and ecological specialization. Molecular Phylogenetics and Evolution. 139.
In the classification system of Dahlgren the Loasaceae were placed in the order Loasales in the superorder Loasiflorae (also called Loasanae). The Angiosperm Phylogeny Group system places them in the related order Cornales in the asterid clade.
Zoological Journal of the Linnean Society 100: 263-326-page(s): 287Rolán E., 2005. Malacological Fauna From The Cape Verde Archipelago. Part 1, Polyplacophora and Gastropoda. Current synonymy follows a revision of Chromodorididae which used molecular phylogeny.
Parapolystichum is a genus of ferns in the family Dryopteridaceae, subfamily Elaphoglossoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). The genus is mainly native to the tropics, although its range extends to southeastern Australia.
Pronephrium is a genus of ferns in the family Thelypteridaceae in the family Thelypteridaceae, subfamily Thelypteridoideae, in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). Other sources sink Pronephrium into a very broadly defined genus Thelypteris.
Gosliner T.M. & Johnson R.F. (1999). "Phylogeny of Hypselodoris (Nudibranchia: Chromodorididae) with a review of the monophyletic clade of Indo-Pacific species, including descriptions of twelve new species". Zoological Journal of the Linnean Society 125(1): 1–114. .
They are also a food source of the paca. Its pollen is shed as permanent tetrads.Walker JW (1971) Pollen Morphology, Phytogeography, and Phylogeny of the Annonaceae. Contributions from the Gray Herbarium of Harvard University, 202: 1-130.
Dasygrammitis is a genus of ferns in the family Polypodiaceae, subfamily Grammitidoideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). It is known from Sri Lanka through southeast Asia and the Philippines to Polynesia.
A time-calibrated phylogeny of Durvillaea based on four mitochondrial and nuclear DNA markers (COI, rbcL, 28S and 18S) indicates the evolutionary relationships shown in the cladogram below. Notably, additional unclassified lineages were estimated within D. antarctica.
In 2016, the Pteridophyte Phylogeny Group divided order Polypodiales into six suborders. Pteridaceae is the sole family in suborder Pteridiineae, with 52 genera. The suborder has the same circumscription as Smith et al. used for the family.
Greengenes is a quality controlled, comprehensive 16S reference database and taxonomy based on a de novo phylogeny that provides standard operational taxonomic unit sets. It is no longer maintained actively and it was last updated in 2013.
Trape & D.G. Broadley (2007) "The phylogeny of cobras inferred from mitochondrial DNA sequences: evolution of venom spitting and the phylogeography of the African spitting cobras (Serpentes: Elapidae: Naja nigricollis complex)". Molecular Phylogenetics and Evolution, 45: 437–453.
As massive quadrupeds, sauropods developed specialized graviportal (weight- bearing) limbs. The hind feet were broad, and retained three claws in most species.Bonnan, M.F. 2005. Pes anatomy in sauropod dinosaurs: implications for functional morphology, evolution, and phylogeny; pp.
Ideally, taxonomic classification should reflect the evolutionary history of the taxa, i.e. the phylogeny. Although some exceptions are present when the phenotype differs amongst the group, especially from a medical standpoint. Some examples of problematic classifications follow.
GARDA, A. A., and D. C. CANNATELLA. 2007. Phylogeny and biogeography of paradoxical frogs (Anura, Hylidae, Pseudae) inferred from 12S and 16S mitochondrial DNA. Molecular Phylogenetics and Evolution. Molecular Phylogenetics and Evolution. 44:104-114.AGUIAR-JR.
Deparia (or the false spleenworts) is a genus of ferns. The Pteridophyte Phylogeny Group classification of 2016 (PPG I) places the genus in the family Athyriaceae, although other sources include it within an expanded Aspleniaceae or Woodsiaceae.
Testing the reliability of the tree after inferring its phylogeny, is a crucial step in the phylodynamic pipeline. Methods to test the reliability of a tree include bootstrapping, maximum likelihood estimation, and posterior probabilities in Bayesian analysis.
Non- homologous exon alignment by an iterative method (a), and by a phylogeny-aware method (b) Most multiple sequence alignment methods try to minimize the number of insertions/deletions (gaps) and, as a consequence, produce compact alignments. This causes several problems if the sequences to be aligned contain non-homologous regions, if gaps are informative in a phylogeny analysis. These problems are common in newly produced sequences that are poorly annotated and may contain frame-shifts, wrong domains or non-homologous spliced exons. The first such method was developed in 2005 by Löytynoja and Goldman.
This led to evolutionary taxonomy, where the various extant and extinct are linked together to construct a phylogeny. This is largely what is meant by the term 'Linnaean taxonomy' when used in a modern context. In cladistics, originating in the work of Willi Hennig, 1950 onwards, each taxon is grouped so as to include the common ancestor of the group's members (and thus to avoid phylogeny). Such taxa may be either monophyletic (including all descendants) such as genus Homo, or paraphyletic (excluding some descendants), such as genus Australopithecus.
The next closest relative outside the genus is the much larger, but similarly marked, blue-faced honeyeater.Driskell, A.C., Christidis, L (2004) Phylogeny and evolution of the Australo-Papuan honeyeaters (Passeriformes, Meliphagidae) Molecular Phylogenetics and Evolution 31 943–960 More recently, DNA analysis has shown honeyeaters to be related to the Pardalotidae (pardalotes), Acanthizidae (Australian warblers, scrubwrens, thornbills, etc.), and the Maluridae (Australian fairy-wrens) in the large superfamily Meliphagoidea.Barker, F.K., Cibois, A., Schikler, P., Feinstein, J., and Cracraft, J (2004) Phylogeny and diversification of the largest avian radiation. Proceedings Natl. Acad. Sci.
The family Capniidae is often considered to be monotypic as to subfamily, with the Capniinae being inserted at that rank. However, this is rather pointless; in any case, the phylogeny, systematics, and taxonomy of the small winter stoneflies are highly confused. There appear to be two very basal genera and presumably two larger clades which conceivably could be considered subfamilies, but the phylogeny of the Capniidae is by no means robustly resolved, with about one-third of the named genera of uncertain position. Hence, any subdivision beyond the generic level is premature.
In the early 21st century, the well-known Hydra and its relatives - and most of the supposed filiferan infraorders Tubulariida and Moerisiida - were determined to be a very ancient lineage, recognized as suborder Aplanulata.Collins, A. G., Winkelmann, S., Hadrys, H. and Schierwater, B. (2005), Phylogeny of Capitata and Corynidae (Cnidaria, Hydrozoa) in light of mitochondrial 16S rDNA data. Zoologica Scripta, 34: 91–99. doi:10.1111/j.1463-6409.2005.00172.x Although not all Anthoathecatae have been firmly placed in the phylogeny, most are fairly certainly assigned at least to one of the major subdivisions.
This is because pairwise distances are not independent; each branch on a tree is represented in the distance measurements of all taxa it separates. Error resulting from any characteristic of that branch that might confound phylogeny (stochastic variability, change in evolutionary parameters, an abnormally long or short branch length) will be propagated through all of the relevant distance measurements. The resulting distance matrix may then better fit an alternate (presumably less optimal) tree. Despite these potential problems, distance methods are extremely fast, and they often produce a reasonable estimate of phylogeny.
Through incorporating this mapping of viral genotype into viral phenotype (or antigenic cluster) into their model, the authors were able to reproduce the ladder-like phylogeny of influenza's HA protein without generalized strain- transcending immunity. The reproduction of the ladder-like phylogeny resulted from the viral population passing through repeated selective sweeps. These sweeps were driven by herd immunity and acted to constrain viral genetic diversity. Instead of modeling the genotypes of viral strains, a compartmental simulation model by Gökaydin and colleagues considered influenza evolution at the scale of antigenic clusters (or phenotypes).
Any attempt at ancestral reconstruction begins with a phylogeny. In general, a phylogeny is a tree-based hypothesis about the order in which populations (referred to as taxa) are related by descent from common ancestors. Observed taxa are represented by the tips or terminal nodes of the tree that are progressively connected by branches to their common ancestors, which are represented by the branching points of the tree that are usually referred to as the ancestral or internal nodes. Eventually, all lineages converge to the most recent common ancestor of the entire sample of taxa.
In 1990, Taylor's lab group published protocols for fungal PCR that were developed in Berkeley by a team including sabbatical visitor, Dr. Thomas J. White (who had directed the development of PCR - polymerase chain reaction - at CETUS corporation), postdoc Thomas D. Bruns and student Steven B. Lee. Their approach has been very influential in fungal evolution and ecology [ ]. Taylor and White continued their collaboration by focusing on the evolution of two human pathogenic fungi, Coccidioides immitis and Histoplasma capsulatum. Taylor and colleagues also applied PCR to fungal phylogeny and fitting phylogeny to geologic time.
She was selected as recipient of the Outstanding Contributions to Cultural Psychology Award from the International Association for Cross-Cultural Psychology in 2018. She received the American Association for the Advancement of Science Award for Behavioral Science Research for her 1991 paper titled Language, tools and brain: The ontogeny and phylogeny of hierarchically organized sequential behavior,Greenfield, P., Andreae, J., Ryan, S., Pepperberg, I., Westergaard, G., & Pinon, P. (1994). Language, tools, and the brain: The ontogeny and phylogeny of hierarchically organized sequential behavior. Behavioral and Brain Sciences, 17(2), 357-365.
The Dioscoreales are an order of monocotyledonous flowering plants in modern classification systems, such as the Angiosperm Phylogeny Group and the Angiosperm Phylogeny Web. Within the monocots Dioscoreales are grouped in the lilioid monocots where they are in a sister group relationship with the Pandanales. Of necessity the Dioscoreales contain the family Dioscoreaceae which includes the yam (Dioscorea) that is used as an important food source in many regions around the globe. Older systems tended to place all lilioid monocots with reticulate veined leaves (such as Smilacaceae and Stemonaceae together with Dioscoraceae) in Dioscoreales.
Gantner Verlag, Rugell, Liechtenstein. (a collaboration with Mary Gibby of the Royal Botanic Garden Edinburgh), evolutionary patterns within plant genera on islands, with emphasis on Echium, the phylogenetic history of Drosera and phylogenetic and taxonomic revision on ActaeaCompton JA, Culham A, Jury SL. 1998 Reclassification of Actaea to include Cimicifuga and Souliea (Ranunculaceae): phylogeny inferred from morphology, nrDNA ITS, and cpDNA trnL-F sequence variation. Taxon 47 (3): 593–634 and Ranunculaceae tribe ActaeaeCompton, J.A. and Culham, A. Phylogeny and circumscription of tribe Actaeeae Ranunculaceae. Systematic Botany, 27 (3) July–September 2002, 502–511.
In 2009, John K. Tucker and Manuel J. Tenorio elevated the subfamily Conorbiinae (at that point it was placed in the family Conidae) to the rank of family. This was based on a cladistical analysis of anatomical characters including the radular tooth, morphology (i.e. shell characters), as well as an analysis of prior molecular phylogeny studies, all of which was used to construct phylogenetic trees. Tucker and Tenorio noted a close relationship to genera such as Bathytoma in their phylogeny, which corresponded to prior molecular studies by Puillandre et al..N.
All the states are accounted for by descent from other states. A cladogram that conforms to these requirements is a perfect phylogeny.. At first there seemed to be little consistency of results in trials varying the factors presumed to be relevant. A new cladogram resulted from any change, which suggested that the method was not capturing the underlying evolution of languages but only reflecting the extemporaneous judgements of the researchers. In order to find the factors that did bear on phylogeny the researchers needed to have some measure of the accuracy of their results; i.e.
11 Mar. 2013. In addition to his theoretical work on systematics and taxonomy, Gauthier continues to study the anatomy and relationships of diapsids, particularly lepidosaurs. His lizard work currently focuses on Scincomorpha, following on a career-long interest in the unusual clade Xantusiidae. He is a principal investigator on the National Science Foundation-funded effort to reconstruct the phylogeny of lizards and snakes (Squamata) using gross anatomy and molecular structure, building on his earlier work in collaboration with Richard Estes and Kevin de Queiroz, which established the most widely accepted phylogeny of the group.
An analysis based on a morphological character matrix also came to this conclusion.Beutel, R., Balke, M., and Steiner, W. E. 2006. The systematic position of Meruidae (Coleoptera, Adephaga) and the phylogeny of the smaller aquatic adephagan beetle families.
Tetramorium hispidum is a species of ant in the family Formicidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012. Cladistics 28(1): 80-112.
Lithurgopsis apicalis, the orange-tipped woodborer, is a species of woodborer bee in the family Megachilidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Habropoda pallida, known generally as the pallid habropoda or white-faced bee, is a species of anthophorine bee in the family Apidae. It is found in Central America and North America.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera.
Criscione, Francesco, et al. (2020) "Where the snails have no name: a molecular phylogeny of Raphitomidae (Neogastropoda: Conoidea) uncovers vast unexplored diversity in the deep seas of temperate southern and eastern Australia." Zoological Journal of the Linnean Society.
Vaginularia is a genus of ferns in the subfamily Vittarioideae of the family Pteridaceae in the Pteridophyte Phylogeny Group classification of 2016 (PPG I). Other sources sink the genus into Monogramma, a genus not recognized in PPG I.
Johnsonia pubescens, commonly called the pipe lily, is a grass-like plant in the family Asphodelaceae, subfamily Hemerocallidoideae,Stevens, P.F. (2001 onwards). "Hemerocallidoideae". Angiosperm Phylogeny Website. Retrieved 2016-06-10. endemic to the south-west of Western Australia.
The currently accepted taxonomy is based on the List of Prokaryotic names with Standing in Nomenclature (LPSN) and NCBI and the phylogeny is based on 16S rRNA-based LTP release 132 by 'The All-Species Living Tree' Project.
The genus is related to Litsea.Chanderbali, A. S., H. van der Werff, and S. S. Renner (2001). Phylogeny and Historical Biogeography of Lauraceae: Evidence from the Chloroplast and Nuclear Genomes. Annals of the Missouri Botanical Garden 88, no.
Endressia is related to Angelica and Selinum in the tribe Selineae. Molecular phylogenetic studies of the angiospermsDouglas E. Soltis, et al. (28 authors). 2011. "Angiosperm Phylogeny: 17 genes, 640 taxa". American Journal of Botany 98(4):704-730.
Coptotriche distincta is a moth of the family Tischeriidae. It was described by Annette Frances Braun in 1972.Global diversity; phylogeny of Tischeriidae It is found in the US state of Arizona. The larvae feed on Quercus hypoleucoides.
Coptotriche splendida is a moth of the family Tischeriidae. It was described by Annette Frances Braun in 1972.Global diversity; phylogeny of Tischeriidae It is found in the US state of California. The larvae feed on Rubus ursinus.
Coptotriche confusa is a moth of the family Tischeriidae. It was described by Annette Frances Braun in 1972.Global diversity; phylogeny of Tischeriidae It is found in the US state of California. The larvae feed on Fragaria species.
Coptotriche inexpectata is a moth of the family Tischeriidae. It was described by Annette Frances Braun in 1972.Global diversity; phylogeny of Tischeriidae It is found in the US state of California. The larvae feed on Fragaria species.
The Benthozoa are a proposed basal Animal clade consisting of the Porifera and Eumetazoa as sister of the Ctenophora. An alternative phylogeny is given by the Porifera-sister hypothesis in which Porifera are the first diverging animal group.
Xolocotzia is a monotypic genusMarx, H. E., et al. (2010). A molecular phylogeny and classification of Verbenaceae. American Journal of Botany 97(10), 1647-63. of flowering plants in the family Verbenaceae containing the single species Xolocotzia asperifolia.
The hindwings are gray with a brown tinge along the front edge., 2006: Phylogeny and life history evolution of Prodoxus yucca moths (Lepidoptera: Prodoxidae). Systematic Entomology 31: 1-20. Adults are on wing from March to early May.
The following cladogram for the suborder Polypodiineae (eupolypods I), based on the consensus cladogram in the Pteridophyte Phylogeny Group classification of 2016 (PPG I), shows a likely phylogenetic relationship between Didymochlaenaceae and the other families of the clade.
Hypisodus was named by Cope (1873). It was assigned to Hypisodontinae by Matthew (1908); and to Hypertragulidae by Cope (1873), Cook (1934) and Carroll (1988).W. D. Matthew. 1908. Osteology of Blastomeryx and phylogeny of the American Cervidae.
Multicalycidae is a family of trematodes in the order Aspidogastrida. It consists of one genus, Multicalyx Faust & Tang, 1936.Faust, E. & Tang, C. (1936). Notes on new aspidogastrid species, with a consideration of the phylogeny of the group.
This species is widely distributed throughout the Indo-West Pacific Oceans including the central Pacific and the Red Sea.Brunckhorst, D.J. (1993) The systematics and phylogeny of Phyllidiid Nudibranchs (Doridoidea). Records of the Australian Museum, Supplement 16: 1-107.
The following cladogram for the suborder Polypodiineae (eupolypods I), based on the consensus cladogram in the Pteridophyte Phylogeny Group classification of 2016 (PPG I), shows a likely phylogenetic relationship between Dryopteridaceae and the other families of the clade.
Phylogeny of the New World true frogs (Rana). Molecular Phylogenetics and Evolution 34:299–314.Pauly et al. (2009)) is a species of leopard frog from the true frog family native to parts of Canada and United States.
Peters, A. F., et al. (1997). Phylogeny and historical ecology of the Desmarestiaceae (Phaeophyceae) support a Southern Hemisphere origin. J Phycol 33 294-309. The third genus, Desmarestia, has 30Guiry, M. D. & G. M. Guiry. 2013. Desmarestia. AlgaeBase.
California Department of Fish and Game. This species was recently moved from the Sebastes subgenus MebarusLi, Z., et al. (2006). Phylogeny of members of the rockfish (Sebastes) subgenus Pteropodus and their relatives. Can. J. Zool. 84 527–36.
The following cladogram for the suborder Polypodiineae (eupolypods I), based on the consensus cladogram in the Pteridophyte Phylogeny Group classification of 2016 (PPG I), shows a likely phylogenetic relationship between Nephrolepidaceae and the other families of the clade.
The following cladogram for the suborder Polypodiineae (eupolypods I), based on the consensus cladogram in the Pteridophyte Phylogeny Group classification of 2016 (PPG I), shows a likely phylogenetic relationship between Davalliaceae and the other families of the clade.
Alansmia is a genus of ferns in the family Polypodiaceae, subfamily Grammitidoideae, according to the Pteridophyte Phylogeny Group classification of 2016 (PPG I). The genus is mainly native to the Neotropics, with a few species in tropical Africa.
Lowry, J.K. & Myers, A.A. (2013) A Phylogeny and Classification of the Senticaudata subord. nov. (Crustacea: Amphipoda). Zootaxa 3610 (1): 1-80. The suborder is defined by a presence of strong apical setae on the 1st and 2nd uropods.
Prenanthella is a monotypic genus of flowering plants in the daisy family.Ford, V. S., et al. (2006). Species divergence and relationships in Stephanomeria (Compositae): PgiC phylogeny compared to prior biosystematic studies. American Journal of Botany 93: 480-90.
The following cladogram for the suborder Polypodiineae (eupolypods I), based on the consensus cladogram in the Pteridophyte Phylogeny Group classification of 2016 (PPG I), shows a likely phylogenetic relationship between Oleandraceae and the other families of the clade.
Ceratophyllidia is a genus of sea slugs, dorid nudibranchs, shell-less marine gastropod molluscs in the family Phyllidiidae.Brunckhorst D. J. (1993) "The systematics and phylogeny of phyllidiid nudibranchs (Doridoidea)". Records of the Australian Museum suppl. 16: 1-108.
Ocnogyna anatolica is a moth of the family Erebidae. It was described by Thomas Joseph Witt in 1980. It is found in Turkey., 2011: "Lymantriinae and Arctiinae - Including Phylogeny and Check List of the Quadrifid Noctuoidea of Europe".
Accessed through: World Register of Marine Species on 2016-12-22.Cella, K; Carmona Barnosi, L.; Ekimova, I; Chichvarkhin, A; Schepetov, D; Gosliner, T. M. (2016). A radical solution: The phylogeny of the nudibranch family Fionidae. PLoS ONE.
Mistakes in phylogeny were likely made when Haeckel characterized different lifecycles as two species. Some of these discrepancies are addressed in the summary of the most recent research on the phylogenetic relationships within Collodaria found in following section.
Phylogeny of the Crocodylotarsi, with reference to archosaurian and crurotarsan monophyly. Journal of Vertebrate Paleontology 13: 287-308. However, a later study found that Batrachotomus was a more basal pseudosuchian only slightly more "advanced" than Prestosuchus.Gower DJ. 2002.
Malaquias et al. (2009)Malaquias M. A. E., Dodds J. M., Bouchet P. & Reid D. G. (2009). "A molecular phylogeny of the Cephalaspidea sensu lato (Gastropoda: Euthyneura): Architectibranchia redefined and Runcinacea reinstated". Zoologica Scripta 38(1): 23-41. .
Ban X., et al. (2018) Tribal classification and phylogeny of Geometrinae (Lepidoptera: Geometridae) inferred from seven gene regions. Zoological Journal of the Linnean Society 184 (3): 653–672. There are about 2,300 described species, mostly from the tropics.
ScaleNet but this family is not monophyletic.Cook, L.G., Gullan, P.J. & Trueman, H.E. 2002. A preliminary phylogeny of the scale insects (Hemiptera: Sternorrhyncha: Coccoidea) based on nuclear small-subunit ribosomal DNA. Molecular Phylogenetics and Evolution 25(1): 43-52.
Stereocyclops (common name: Brazilian dumpy frogs) is a small genus of microhylid frogs. It is endemic to the Atlantic forest of eastern Brazil. Molecular phylogeny suggests that it is sister taxon to the clade containing Dasypops and Myersiella.
The Journal of the Entomological Research Society is a peer-reviewed scientific journal published by the Gazi Entomological Research Society. It focus on several aspects of entomology, particularly those related to taxonomy, phylogeny, biodiversity, ecology, aquaculture and morphology.
Boraginoideae is a subfamily of the flowering plant family Boraginaceae s.s, with about 42 genera. That family is defined in a much broader sense (Boraginaceae s.l.) in the Angiosperm Phylogeny Group (APG) system of classification for flowering plants.
Malaquias et al. (2009)Malaquias M. A. E., Dodds J. M., Bouchet P. & Reid D. G. (2009). "A molecular phylogeny of the Cephalaspidea sensu lato (Gastropoda: Euthyneura): Architectibranchia redefined and Runcinacea reinstated". Zoologica Scripta 38(1): 23-41. .
The following cladogram for the suborder Polypodiineae (eupolypods I), based on the consensus cladogram in the Pteridophyte Phylogeny Group classification of 2016 (PPG I), shows a likely phylogenetic relationship between Lomariopsidaceae and the other families of the clade.
"Phylogeny and taxonomy of the Prenolepis genus-group of ants (Hymenoptera: Formicidae)". Systematic Entomology 35 (1): 118-131. These ants are about one- eighth inch long and are covered with reddish-brown hairs. The colonies have multiple queens.
The Senegalese Specimens of Pipistrellus Rueppellii can be confidently assigned to P.r. senegalensis, which is distributed from Algeria to Senegal. After testing the influence of phylogeny, Pipistrellus Rueppellii was found to be basal to the Pipistrellus/Nyctalus clade.
This second clade would be termed Laurasiformes under the group's definition. Brachiosaurus was in a polytomy with the two subclades of Brachiosauridae. The phylogeny of Royo-Torres et al. (2017) can be seen above, in the right column.
The following cladogram for the suborder Polypodiineae (eupolypods I), based on the consensus cladogram in the Pteridophyte Phylogeny Group classification of 2016 (PPG I), shows a likely phylogenetic relationship between Hypodematiaceae and the other families of the clade.
Phylogeny and generic interrelationships of the Stylidiaceae (Asterales), with a possible extreme case of floral paedomorphosis. Systematic Botany, 23(3): 289-304. Donatioideae and Stylidioideae were described by Johannes Mildbraed in his 1908 taxonomic monograph of the family.
This species occurs in Vietnam.Köhler F. & Dames C. (2009). "Phylogeny and systematics of the Pachychilidae of mainland Southeast Asia – novel insights from morphology and mitochondrial DNA (Mollusca, Caenogastropoda, Cerithioidea)". Zoological Journal of the Linnean Society 157: 679-699. .
Earliest known unequivocal rhinocerotoid sheds new light on the origin of Giant Rhinos and phylogeny of early rhinocerotoids. Scientific Reports 6:39607:1-9 Unaware that Wood (1932) made turgaica the type species of Allacerops, Reshetov et al.
Compared to other jerboas in the same genus, Iranian jerboas are most related to Allactaga hotsoni.Dianat, Malahat. "Molecular Phylogeny of the Iranian Plateau Five-toed Jerboa, Allactaga (Dipodidea: Rodentia), Inferred from MtDNA." Mammalia Winter 77.1 (2012): 98. Print.
Molecular phylogeny and taxonomy of the fern genus Anisocampium (Athyriaceae). Taxon 60(3) 824-30. but the genus has since been sunk into Athyrium. This deciduous fern has a creeping rhizome and a tuft-shape array of fronds.
Albumins found in animals can be divided into six subfamilies by phylogeny. The Vitamin-D binding proteins occupy families 1–3. The other albumins are mixed among each other in families 4–6. ECM1 is in family 6.
"Tofieldiaceae" At: Angiosperm Phylogeny Website. At: Botanical Databases At: Missouri Botanical Garden Website. (see External links below) Before the segregation of Tofieldiaceae was confirmed by cladistic methods, its genera had usually been assigned to Nartheciaceae,Minoru N. Tamura. 1998.
E. J. H. Corner suggested moving the genus to the Urticaceae in 1962, while Cornelis Berg placed Cecropia in its own family, the Cecropiaceae. Based on molecular data, the Angiosperm Phylogeny Group merged the family back into the Urticaceae.
Dryocosmus imbricariae, the banded bullet gall wasp, is a species of gall wasp in the family Cynipidae.Sharkey M.J. (2007). Phylogeny and Classification of Hymenoptera."Phylogenetic relationships among superfamilies of Hymenoptera", Sharkey M.J., Carpenter J.M., Vilhelmsen L., et al. 2012.
Muller, J. and Reisz, R.R. (2006). "The phylogeny of early eureptiles: Comparing parsimony and Bayesian approaches in the investigation of a basal fossil clade." Systematic Biology, 55(3):503-511. The same results were obtained in later phylogenic analyses.
"North American freshwater snails". Transactions of the POETS Society 1(4):217-365.Jackiewicz M. (1993). "Phylogeny and relationships within the European species of the family Lymnaeidae". Folia Malacologica 5: 61-95.Glöer P. & Meier-Brook C. (1998). Süsswassermollusken.
Its holotype, specimen MCSNT 11430, was discovered in Slovenia and lived alongside the related Carsosaurus.M.W. Caldwell and A. Palci. 2007. "A new basal mosasauroid from the Cenomanian (U. Cretaceous) of Slovenia with a review of mosasauroid phylogeny and evolution".
Early evolution and higher-level phylogeny of sauropod dinosaurs. Journal of Vertebrate Paleontology, 18(S2), 1-79. A reduction to two carpals, long metacarpals relative to the radius, and a twisted ischial shaft serve to identify the appendicular skeleton.
Coptotriche insolita is a moth of the family Tischeriidae. It was described by Annette Frances Braun in 1972.Global diversity; phylogeny of Tischeriidae It is found in the US state of New Jersey. The larvae feed on Vaccinium corymbosum.
Most of the genera of Lamiaceae have never been sampled for DNA for molecular phylogenetic studies. Most of those that have been are included in the following phylogenetic tree. The phylogeny depicted below is based on seven different sources.
Time-calibrated phylogeny recovered by Shaffer et al. (2017) dated the split of Pantestudines from its sister clade (the clade containing archosaurs and all tetrapods more closely related to archosaurs than to any other living animals) to mid-Carboniferous.
It is thought that Litargosuchus pursued its prey much like a wolf; however, Litargosuchus were likely solitary.Randall, B., Sterling, J. and Sues, H.D., 2013. Early Crocodylomorpha. Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and Their Kin, (379), p.275.
C. H. Beck'sche Verlagsbuchhandlung, München 161-332.Heckert, A. B. and Lucas, S. G. (2000). Taxonomy, phylogeny, biostratigraphy, biochronology, paleobiogeography, and evolution of the Late Triassic Aetosauria (Archosauria: Crurotarsi). Zentralblatt für Geologie und Paläontologie Teil I 1998:1539–1587.
McEachran and Neil Aschliman in 2004 found Plesiobatis to be the sister taxon of Urolophus, and recommended that it be placed in the family Urolophidae. Until the phylogeny is better-resolved, authors have tended to preserve the family Plesiobatidae.
The superfamily Lymexyloidea is currently within series Cucujoidea. The internal phylogeny has not been clearly understood/completed by experts. Morphological data places the family inside the Tenebrionoidea, while molecular data place it as sister taxon to Tenebrionoidea, and polyphyletic.
"Taxonomy and phylogeny of new wood- and soil-inhabiting Sporothrix species in the Ophiostoma stenoceras-Sporothrix schenckii complex." Mycologia 100(4): 647–661. and pathogenicRita Marimon, Josep Cano, Josepa Gene, Deanna A. Sutton, Masako Kawasaki, and Josep Guarro (2007).
In the circulatory system the haemolymph circulates as follows: mantle → nephridium or nephridia → heart. These slugs breathe using a pallial lung. They have a contractile pneumostome.Barker G. M. (2001) Gastropods on Land: Phylogeny, Diversity and Adaptive Morphology. 1-146.
Ophiuroid phylogeny and higher taxonomy: morphological, molecular and palaeontological perspectives. Zool. J. Linn. Soc. 114 (1995) Some recent data suggest its relationship to the extant family Ophiomyxidae (it would thus belong to the order Phrynophiurida).Pearse,V.B. et al.
Least squares inference in phylogeny generates a phylogenetic tree based on an observed matrix of pairwise genetic distances and optionally a weight matrix. The goal is to find a tree which satisfies the distance constraints as best as possible.
Pennisetum is closely related to the genus Cenchrus,Martel, E., et al. (2004). Chromosome evolution of Pennisetum species (Poaceae): implications of ITS phylogeny. Plant Systematics and Evolution 249(3-4), 139-49. and the boundary between them is unclear.
Ophiocomidae has been placed (along with Ophionereididae) to the superfamily Ophiocomidea and infraorder GnathophiurinaSmith, A.B.; Paterson, G.L.J., Ophiuroid phylogeny and higher taxonomy: morphological, molecular and palaeontological perspectives. Zool. J. Linn. Soc. 114 (1995) or suborder Gnathophiurina in different classifications.

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