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180 results for “homoplasy”
Figure 3 in Homoplasy in shells discombobulated the taxonomy: revision of the larger helicarionid land snails of northern Queensland, Australia (Stylommatophora: Helicarionidae)
Figure 3. Comparison of intra- and interspecific genetic p distances for mitochondrial gene COI.
FIG. 4 in Phylogenetic analysis of the red algal tribe Ceramieae reveals multiple morphological homoplasies but defines new genera
FIG. 4. — Reconstruction of character evolution by mapping morphological characters onto the Bayesian tree inferred on rbcL gene. Geographical distribution is given for all the samples. Values at the nodes represent posterior probability, values <0.8 are not shown. Abbreviations: See Figure 3.
Data from: Step matrices and the interpretation of homoplasy
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Data from: Homoplasy-based partitioning outperforms alternatives in Bayesian analysis of discrete morphological data
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Data from: Testing and quantifying phylogenetic signals and homoplasy in morphometric data
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Data from: Tip-dating and homoplasy: reconciling the shallow molecular divergences of modern gharials with their long fossil record
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Data from: When homoplasy is not homoplasy: dissecting trait evolution by contrasting composite and reductive coding
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Data from: True homoplasy of retrotransposon insertions in primates
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Data from: Evolution of the snake body form reveals homoplasy in amniote Hox gene function
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FIGURE 10 in A new species of Ungla (Neuroptera: Chrysopidae) that exhibits remarkable homoplasy in male secondary sexual characters
FIGURE 10. Male cranial features of Ungla pseudomeleoma and selected Meleoma species. A, B Ungla pseudomeleoma, sp. nov., Holotype (Peru: La Libertad, FSCA). A. Lateral; B. Frontolateral (arrows in both A and B indicate paired arms of the interantennal and lower horns); C. Meleoma hageni Banks (USA: Arizona, TRC), lateral (downward-facing arrows indicate interantennal and lower horns, upward-facing arrow indicates horn within frontal cavity); D. Meleoma furcata (Banks) (USA: Arizona, TRC), lateral (arrow indicates horn within frontal cavity); E. Meleoma stangei Penny (Mexico: Baja California, San Diego County Museum of Natural History), lateral (arrow indicates double horn within frontal cavity); F. Meleoma undescribed sp. #1 (USA: Arizona, TRC), frontolateral (arrow indicates horn within frontal cavity; note absence of interantennal and lower horns).
FIGURE 3 in A new species of Ungla (Neuroptera: Chrysopidae) that exhibits remarkable homoplasy in male secondary sexual characters
FIGURE 3. Ungla pseudomeleoma, sp. nov., Exterior head and body (male, Peru: La Libertad). A. Holotype, head (ventral, FSCA); B. Paratype, head, prothorax (dorsal, TRC); C. Holotype, body (lateral, FSCA); D. Holotype, head and thorax (lateral, FSCA); E. Holotype, abdomen (lateral, FSCA); F. Holotype, terminus (lateral, FSCA). c.c., callus cerci; S4, fourth sternite; S8+9, fused eighth and ninth sternites, sc, scape; sp, spiracular openings.
Fig. 3 in Phenotypical plasticity and homoplasy complicate species delimitation in the Cladonia gracilis group (Cladoniaceae, Ascomycota)
Fig. 3 Results of PTLPT analysis, actual tree length compared to the tree lengths for 1,000 artificially recombined
Fig. 1 in Phenotypical plasticity and homoplasy complicate species delimitation in the Cladonia gracilis group (Cladoniaceae, Ascomycota)
Fig. 1 Phylogeny of the C. gracilis group. 50% Majority Rule Bayesian tree based on a combined data set including ITS rDNA, IGS and RPB2. Branches supported with posterior probability ≥0.95 and
Figure 9 in High level of phenotypic homoplasy amongst eutardigrades (Tardigrada) based on morphological and total evidence phylogenetic analyses
Figure 9. Majority rule phylogram that best fitted current Eutardigrada classification (Marley et al., 2011), obtained with PAUP for parsimonious analyses using the reduced morphological matrix, that is, without any homoplastic characters. Values above branches are parsimonious bootstrap supports after 1000 replicates. Values under branches are Bremer relative supports. Superfamilies with associated claw morphologies and families are indicated.
Figure 6 in High level of phenotypic homoplasy amongst eutardigrades (Tardigrada) based on morphological and total evidence phylogenetic analyses
Figure 6. Maximum clade credibility phylogram obtained with Bayesian inference using the complete morphological matrix without gamete-related characters. Values above branches are posterior probabilities supports. Scale bar indicates nucleotide substitutions per site.
Figure 3 in Mosaic patterns of homoplasy accompany the parallel evolution of suspensory adaptations in the forelimb of tree sloths (Folivora: Xenarthra)
Figure 3. Boxplots and ancestral state reconstructions of select linear measurements and angles. Metrics were selected to represent the diversity of observed outcomes, including one example (A) of a trait that is clearly distinct between tree sloths and other taxa, one example (B) of a trait that exhibits significant convergence between tree sloths but not a significant difference between tree sloths and other xenarthrans, and one example (C) of a trait for which tree sloths do exhibit a significant difference with other xenarthrans, but do not exhibit clear evidence of convergence. Ancestral state reconstructions are provided to visualize changes in a phylogenetic context and are not necessarily intended to accurately characterize ancestral states, although they do represent the states used to measure convergence. In the heatmaps, purple represents the direction predicted for suspensory taxa.
Figure 2 in Mosaic patterns of homoplasy accompany the parallel evolution of suspensory adaptations in the forelimb of tree sloths (Folivora: Xenarthra)
Figure 2. Landmarks and measurements taken in this study. Top row: scapulae shown are (from left to right) Bradypus, Choloepus, Tamandua, Tamandua. Long bones shown are from Tamandua (from left to right): humerus (anterior), humerus (posterior), ulna, tibia, femur, radius, radius (proximal).
Figure 23 in Homoplasy in shells discombobulated the taxonomy: revision of the larger helicarionid land snails of northern Queensland, Australia (Stylommatophora: Helicarionidae)
Figure 23. Genitalia of Elatonitor montanus. a) QM MO38930, Bellenden Ker Range. Reproductive system. b) QM MO78930, Bellenden Ker Range. Penis interior. c) QM MO11240, Bellenden Ker summit. Penis interior. Scale bars: 1 mm.
Figure 14 in Homoplasy in shells discombobulated the taxonomy: revision of the larger helicarionid land snails of northern Queensland, Australia (Stylommatophora: Helicarionidae)
Figure 14. Shells of Pravonitor. a) Pravonitor insularum, AM C.170795 (paratype). b) Pravonitor annulus AM C.425415, Gabba Is. c) Pravonitor aquilonia, QM MO48285 (holotype). d) Pravonitor ferrugineus, QM MO12752 (holotype). e). Pravonitor kreffti, AM C.1352, Thursday Is. f) Pravonitor kreffti, AM C.425474, Simpson's Bay, Utingu. g) Pravonitor monteithi, QM MO48587 (holotype). h) Pravonitor septentrionalis, AM C.425422. i) Pravonitor stuarti, QM MO80213 (paratype). Scale bar: 5 mm.
Figure 20 in Homoplasy in shells discombobulated the taxonomy: revision of the larger helicarionid land snails of northern Queensland, Australia (Stylommatophora: Helicarionidae)
Figure 20. Genitalia of Pravonitor septentrionalis. a-c) QM MO86001 (holotype), Lockerbie. a) Reproductive system. b) Penis interior. c) Penial complex. d) QM MO15621 (paratype), Bamaga. Spermatophore. Scale bars: 1 mm.
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