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128 results for “Cladogram”
Figure 5. Cladogram depicting the phylogenetical relationships among Parotoplana species. 50 in The genera Parotoplana Meixner, 1938 and Parotoplanella Ax, 1956 (Platyhelminthes: Proseriata) in southern Spain
Figure 5. Cladogram depicting the phylogenetical relationships among Parotoplana species. 50% majority rule and, when present, Bremer support values are indicated at nodes. New species in bold.
FIGURE 7. Taxon Area Cladograms for A in Phylogeny and an integrated biogeography of Acanthotetilla Burton, 1959 (Demospongiae: Spirophorida: Tetillidae): two-way traffic on the peri-African track
FIGURE 7. Taxon Area Cladograms for A. Mycale immitis (Schmidt, 1870) group; B. Mycale australis (Gray, 1867) group [= M. (Grapelia) spp. sensu Van Soest et al. (2011)]; C. Thrinacophora Ridley, 1885; D. Acarnus Gray, 1867; E. Didiscus Dendy, 1922; F. Placospongia Gray, 1867; G. Rhabderemia Topsent, 1890 and H. Petromica Topsent, 1898. A–E from Van Soest & Hajdu (1997). F. from Nichols and Barnes (2005). G. from Hajdu & Desqueyroux-Faúndez (2008). H. from List-Armitage & Hooper (2002). Areas utilized in the original biogeographic analyses were transformed into Spalding et al.'s (2007) provinces (Table 4). The black circles indicate cladogenetic events separating the areas considered in the TAC-TAC comparisons performed.
FIGURE 240. Cladogram from trees obtained with K in <strong>Phylogeny and Revision of <em>Toechorychus</em> Townes (Hymenoptera, Ichneumonidae, Cryptinae), with descriptions of thirty-five new species</strong>
FIGURE 240. Cladogram from trees obtained with K=1 and 2 (identical). Numbered circles represent synapomorphies, with the respective character and state number. Black circles indicate the non-homoplasious synapomorphies, 152:1 and 153:1. The arrows indicate these character-states at the ovipositor illustration. Abbreviations: GABN, Gabuniina; GORY, Goryphina; LYMN, Lymeonina; MEST, Mesostenina.
Figure 5. Agreement subtree cladogram obtained with the Ratchet algorithm for parsimonious analyses using the complete morphological matrix without gamete-related characters. Values above branches are bootstrap supports after 1000 in High level of phenotypic homoplasy amongst eutardigrades (Tardigrada) based on morphological and total evidence phylogenetic analyses
Figure 5. Agreement subtree cladogram obtained with the Ratchet algorithm for parsimonious analyses using the complete morphological matrix without gamete-related characters. Values above branches are bootstrap supports after 1000 replicates; values under branches are Bremer relative supports.
FIGURE 3. Most-parsimonious cladogram derived from 12S in A systematic review of the genus Chasmodes (Teleostei: Perciformes: Blenniidae)
FIGURE 3. Most-parsimonious cladogram derived from 12S DNA sequences from ten blenniid species. Length = 179 steps, CI = 0.65, RI = 0.85. In cases where multiple specimens of a species are present, collection numbers are listed. Support values are to left of nodes, bootstrap values above and Bremer support values below.
Figure 1. Cladogram obtained under K in Phylogenetic analysis of the tribe Macropelopiini (Chironomidae: Tanypodinae): adjusting homoplasies
Figure 1. Cladogram obtained under K = 5. The numbers above the nodes represent, from left to right the absolute and relative Bremer supports, respectively.
Figure 23. Temporally calibrated cladogram representing a in The skull of the titanosaur Tapuiasaurus macedoi (Dinosauria: Sauropoda), a basal titanosaur from the Lower Cretaceous of Brazil
Figure 23. Temporally calibrated cladogram representing a reduced consensus of 34 MPTs generated in a cladistic analysis of 31 taxa and 246 characters (see text for details). The reduced consensus was generated using the iterPCR script in TNT (see Pol & Escapa, 2009), which identified Tapuiasaurus and Nemegtosaurus as wildcard taxa that linked with 13 different lithostrotian taxa in the MPTs (labelled a–c and d–m, respectively). The italicized numbers at nodes within Titanosauria represent decay indices>1. The coloured bars represent the temporal distribution of diplodocoid (brown) and macronarian (purple) taxa; in all cases their vertical extent reflects stratigraphic uncertainty rather than a true range. Dates at epoch and stage boundaries are based on Cohen et al. (2013). Coloration of chronostratigraphic units follows the Commission for the Geological Map of the World (http://www.ccgm.org).
Figure 6. Gondwana area cladogram and a in New morphological evidence supports congruent phylogenies and Gondwana vicariance for palaeognathous birds
Figure 6. Gondwana area cladogram and a fully resolved palaeognath phylogeny (based on Fig. 4A) mapped together and reconciled with TREEMAP (http://taxonomy.zoology.gla.ac.uk/rod/treemap.html). Circles indicate nodes on the palaeognath tree that occur prior to geographical separations.
Figure 11. Cladogram, selected from 36 minimal length trees with 125 in The larval head of Nevrorthidae and the phylogeny of Neuroptera (Insecta)
Figure 11. Cladogram, selected from 36 minimal length trees with 125 steps (NONA, heuristic search, 1000 replications). Apomorphies mapped on tree, nonhomoplasious changes full quadrangles (* apomorphies only in ACCTRAN and DELTRAN optimization). Bremer support values in circles.
FIGURE 9. Rooted cladogram showing phylogenetic relationships among four genera, i.e in Serina Gredler (Gastropoda, Stylommatophora: Enidae), the continuous-peristomed mountain snails endemic to the eastern slope of the Qinghai-Xizang Plateau
FIGURE 9. Rooted cladogram showing phylogenetic relationships among four genera, i.e. Serina (S. ser, S. prostoma, S. subser, S. egressa, S. denticulate n. sp.), Clausiliopsis (C. szechenyi), Pupopsis (P. pupopsis), and Holcauchen (H. sulcata). Outgroup Pupinidius (P. wenxian, P. latilabrum, P. melinostoma, P. nanpingensis). Branch length 45, CI=0.60, RI=0.70. Explanation for characters and character states see in Table 6. Solid circle: nonhomoplasious change; open circle: homoplasious change.
FIGURE 11. Most parsimonious cladogram obtained for Thyroptera Spix, 1823. A in Hershkovitzia (Diptera: Nycteribiidae): revision, phylogeny, and cophylogeny
FIGURE 11. Most parsimonious cladogram obtained for Thyroptera Spix, 1823. A. Cladogram with DELTRAN optimization of the characters (L=64, CI=62, RI=61). B. Same, with numbers above the branches indicating Bootstrap support and numbers below the branches indicating decay index (Bremer support).
FIGURE 18. Partial cladogram modified from Taylor & Knouft 2006 showing Clade D in Review of crayfish color patterns in the Family Cambaridae (Astacoidea), with discussion of their possible importance
FIGURE 18. Partial cladogram modified from Taylor & Knouft 2006 showing Clade D.
Fig. 1. Cladogram depicting hypothesized relationships among Clade A in Systematics of the Neotropical fish subfamily Glandulocaudinae (Teleostei: Characiformes: Characidae)
Fig. 1. Cladogram depicting hypothesized relationships among Clade A characids as modified here from Malabarba & Weitzman (2003) with indication of non-inseminating and inseminating groups.
text-fig. 56. Phylogram of theropod relationships, based on the cladogram in ext-figure 55. in The interrelationships and evolution of basal theropod dinosaurs
text-fig. 56. Phylogram of theropod relationships, based on the cladogram in ext-figure 55.
Text-fig. 13: Cladogram showing the systematic position of Protothymallus within the Gobioninae, (for the character states see Tab. 1 and text). in Revision Of The Cyprinids From The Early Oligocene Of The České Středohoří Mountains, And The Phylogenetic Relationships Of Protothymallus Laube, 1901 (Teleostei, Cyprinidae, Gobioninae)
Text-fig. 13: Cladogram showing the systematic position of Protothymallus within the Gobioninae, (for the character states see Tab. 1 and text).
Fig. 11. Cladogram depicting hypothesized relationships among Clade A in Putative relationships among inseminating and externally fertilizing characids, with a description of a new genus and species of Brazilian inseminating fish bearing an anal-fin gland in males (Characiformes: Characidae)
Fig. 11. Cladogram depicting hypothesized relationships among Clade A characids as modified here from Malabarba and Weitzman (2003) with the addition of Bryconadenos shown as a sister group of Attonitus and the placement of genera with inseminating species as possibly more closely related to one another than to non-inseminating Clade A genera.
Fig. 128. Cladogram showing relationships between Characidae lacking a in Phylogeny of the family Characidae (Teleostei: Characiformes): from characters to taxonomy
Fig. 128. Cladogram showing relationships between Characidae lacking a supraorbital bone (Astyanax clade, Astyanax paris clade, Bryconamericus scleroparius clade, Hyphessobrycon luetkenii clade, and Gymnocharacinae). Node numbers correspond to those in the text.
Figures 315–316. Vatellini species, consensus cladograms. 315 in Revision of the New World and south-east Asian Vatellini (Coleoptera: Dytiscidae: Hydroporinae) and phylogenetic analysis of the tribe
Figures 315–316. Vatellini species, consensus cladograms. 315, Consensus cladogram of 72 most parsimonious cladograms (length = 78, CI = 67, RI = 92) resulting from cladistic analysis of Vatellini including Calicovatellus petrodytes. 316, Consensus cladogram of five most parsimonious cladograms (length = 74, CI = 70, RI = 93) resulting from cladistic analysis of Vatellini not including Calicovatellus petrodytes. Numbers above branches are Bremer support values.
Figure 8. Cladogram 6 in Phylogenetic analysis of Eurytominae (Chalcidoidea: Eurytomidae) based on morphological characters
Figure 8. Cladogram 6. Phylogeny of the species classified in Eurytoma: strict consensus tree (CS) of the equally weighted trees (n = 2). Study carried out with 156 morphological characters and 37 taxa (Analysis 3). Bootstrap values are given above the branches. Length of the tree: 188.58; consistency index, CI = 0.388; retention index, RI = 0. 791; rescaled consistency index, RC = 0.307. The generic groups, the large genera, and some species groups, as defined in the text, are shaded. The dentata species group is not monophyletic on this cladogram.
Data from: Cladograms, phylogenies and the veracity of the conodont fossil record
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