homoplasy

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ho·mo·pla·sy

 (hō′mə-plā′sē, -plăs′ē, hŏm′ə-)
n.
Correspondence between parts or organs arising from evolutionary convergence.

ho•mop•la•sy

(həˈmɒp lə si, ˈhoʊ məˌplæs i, -ˌpleɪ si, ˈhɒm ə-)

n.
correspondence in biological form or structure, owing to convergent evolution.
[1865–70]
ho•mo•plas•tic (ˌhoʊ məˈplæs tɪk, ˌhɒm ə-) adj.
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Black circles indicate sinapomorfies for the generalized tracks: 14= Crotalus aquilus, 18= Crotalus ravus, 61= Storeira hidalgoensis, 75= Thamnophis sumichrasti, 31= Geophis mutitorques, 32=Geophis semidoliatus, 44= Micrurus tener, 55= Rhadinea gaigeae, 2= Agkistrodon taylori, 20= Crotalus totonacus, 42= Micrurus bernadi, 51= Pliocercus elapoides, 56= Rhadinaea marcellae, 57= Rhadinaea quinquelineata, 78= Chersodromus rubriventris 80= Geophis turbidus 81= Lampropeltis ruthveni, white circles indicate homoplasies. Bootstrap values are shown below nodes.
Those authors studied recombinant MERS to investigate excessive homoplasies, decay of linkage disequilibrium and the presence of alternative topologies, and their study showed that the MERS genome has well-supported alternative tree topologies and some degree of rate heterogeneity.
De plus, puisqu'il semble n'exister qu'un nombre limite de solutions structurales a un probleme fonctionnel donne, les homoplasies, ou ressemblances trompeuses entre les organismes adaptes a des modes de vie similaires peuvent induire en erreur l'observateur exterieur qui considere que ces ressemblances signifient des mecanismes adaptatifs similaires alors qu'il peut n'en etre rien (par exemple, ressemblance entre le dauphin et le requin).
Because of the low number of homoplasies expected (18), a neighbor-joining tree was obtained by using MEGA5 (23), with observed number of substitutions as a measure of genetic distance.
The Baileyans utilized these homoplasious characters even though it was recognized by, at the latest, the time of Darwin that homoplasies are useless for the inference of relationships.
It has been shown that shell characters in gastropod phylogeny reconstructions are no more prone to homoplasies than are other types of morphological characters (Schander & Sundberg 2001).
MCs differ from noisy characters (random data sensu Wenzel & Siddall 1999) in that they include not only homoplasies that result from random processes, but also those caused by processes of evolutionary convergence (adaptive and nonadaptive), by among lineages differences in life history traits, or by structural, functional and developmental constraints.
Morphological evolution, aptations, homoplasies, constraints, and evolutionary trends: catfishes as a case study on general phylogeny and macroevolution.
By knowing which species are closely related to which other ones we can test hypotheses of morphological synapomorphies (homology) and homoplasies. Developmental, genetic, and genomic data permit an even deeper analysis of characters, their similarities and their differences.
When homoplasies have arisen from common functional demands (by convergence or parallelism), then spatial or temporal variation in those demands could also select for similarities in the plastic expression of those traits (Hodin, 2000; Meinzer, 2003).
There are no homoplasies in tarsal scopula evolution in the second cladogram.