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Fig. 29 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 29. Occlusal view of m1 in selected phyllostomids. A. Desmodus rotundus (AMNH 174303) B. Phyllostomus hastatus (AMNH 267905). C. Brachyphylla cavernarum (AMNH 208181). D. Phyllonycteris poeyi (AMNH 103542). E. Glossophaga soricina (AMNH 209354). F. Rhinophylla pumilio (AMNH 266192). G. Chiroderma villosum (AMNH 267191). H. Ardops nicholsi (AMNH 213954). I. Sphaeronycteris toxophyllum (AMNH 262637). Scale bar = 1 mm.
Fig. 2 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 2. Intergeneric relationships of phyllostomid bats proposed by de la Torre (1961; redrawn from fig. 4). This tree is based on dental morphology. Vampyressa is not connected to the tree in the original figure.
Fig. 36 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 36. Cross sections of the tongues of A. Desmodus rotundus and B. Lonchophylla robusta illustrating differences between the lingual sulci in these species (redrawn from Griffiths and Criley 1989: fig. 2). Note that the sulci of Desmodus are ventral to the lingual nerve (ln), but in Lonchophylla the sulci are dorsal to this structure.
Fig. 4 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 4. Slaughter (1970; redrawn after fig. 5) proposed this tree of phyllostomids relationships based on dental character evolution. The original caption read ''Dental morphology tree suggesting types of dentition possessed by ancestral forms of chiropteran groups. Generic names are used merely to denote certain types and/or grades of dental forms.''
Fig. 15. A in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 15. A. Gimenez et al.'s (1996; redrawn from fig. 3) cladogram depicting relationships among nectar feeders based on lingual characters. B. Gimenez et al.'s (1996; redrawn from fig. 4) cladogram depicting relationships among nectar feeders based on lingual and hyoid characters.
Fig. 41 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 41. Semidiagrammatic illustrations of the dorsal brain in three phyllostomids illustrating the range of variation in coverage of the inferior colliculi (ic) by the cerebellar vermis. A. Mimon crenulatum. B. Mesophylla macconnelli. C. Lichonycteris obscura (drawn from McDaniel, 1976: figs. 2, 20, 42).
Fig. 46 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 46. Results of a heuristic search of 17 hyoid characters for 27 taxa. The tree shown here is a strict consensus of 24 most parsimonious trees, each of 40 steps (CI = 0.625, RI = 0.893)
Fig. 6 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 6. Gardner's (1977a; redrawn from fig. 8) ''arbitrarily derived'' tree of phyllostomid relationships based on chromosomal similarities. Asterisks indicate taxa that were karyotypically unknown and whose placement was conjectural.
Fig. 44 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 44. Results of a heuristic search of 38 pelage and integument characters for all 63 taxa. The tree shown here is a strict consensus of more than 30,000 most parsimonious trees, each of 183 steps (CI = 0.503, RI = 0.789).
Fig. 40 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 40. Diagram illustrating the two different types of attachment of the ovary to the uterus via the ovarian ligament: A. to the external oviductal entry, or B. to the lateral uterine wall (redrawn from Hood and Smith, 1983: fig. 15).
Fig. 21 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 21. Anterior view of the noseleaf in A. Carollia perspicillata (AMNH 266144) B. Uroderma bilobatum (AMNH 268564) C. Ariteus flavescens (AMNH 214944). Scale bar = 2 mm.
Fig. 32 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 32. Dorsal surface of the tongue in selected noctilionoids. A. Pteronotus davyi (AMNH 175276). Insets from top to bottom: basketlike papilla, basinshaped medial posterior mechanical papilla, lateral circumvallate papilla. B. Noctilio leporinus (AMNH 175534) C. Desmodus rotundus (AMNH 210962). Scale bar = 2 mm.
Fig. 28 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 28. Occlusal view of M1M3 in selected phyllostomids. A. Desmodus rotundus (AMNH 174303). Only M1 is present. B. Chrotopterus auritus (AMNH 267852). C. Brachyphylla cavernarum (AMNH 208181). D. Phyllonycteris poeyi (USNM 103542). E. Monophyllus redmani (AMNH 236662). F. Artibeus jamaicensis (AMNH 266331). Scale bar = 1 mm.
Fig. 33 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 33. Dorsal surface of the tongue in selected phyllostomids. Lowest inset is of a lateral circumvallate papilla. A. Phyllonycteris poeyi (AMNH 23762). B. Glossophaga soricina (AMNH 237911) Lonchophylla thomasi (AMNH 266107). Upper inset: basketlike papilla. Scale bar = 2 mm.
Fig. 1 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 1. The pace of discovery of currently recognized phyllostomid taxa described from 1750 to 1993. A. Genera. B. Species. There has been a steady decrease in the rate of description of new genera since the early 1800s, but the pace of description of new species has not declined at the same rate. We used dates of publication from Koopman (1993).
Figure 3 in Aedeagus evolution promotes speciation? A primary pattern in rove beetle phylogeny
Figure 3. Plotting Paramere-to-Median-lobe Index (PM Index) and the number of species of the selected genera (Y axis) with the divergence time (X axis) estimated. PM Index variations along with divergence time (a, c); species number variations along with evolutionary time (b, d). The abbreviation of geological ages are as follows: Jur—Jurassic; Cre—Cretaceous; Pal—Paleocene; Eoc— Eocene; Oli—Oligocene; Mio—Miocene; Pli—Pliocene.
Figure 2. Figure 2 in Aedeagus evolution promotes speciation? A primary pattern in rove beetle phylogeny
Figure 2. Figure 2. Phylogeny of the subfamily Staphylininae with divergence time estimates based on the concatenated sequence. Blue bars at each node show 95% highest posterior density interval for the main nodes. Colored branches and circled capital letters are as in Figure 1. Circled numbers refer to three main sub-clades within Clade A discussed in text. Circled roman letters represent the calibration points. Capital letter 'A', 'P' and 'N' represent aedeagus, paramere and species number of each corresponding genus respectively. Colored arrows refer to phylogenetic patterns of aedeagus morphology discussed in text. Dot lines with lower case letters refer to divergence times discussed in text. The abbreviation of geological ages are as follows: Jur—Jurassic; Cre—Cretaceous; Pal— Paleocene; Eoc—Eocene; Oli—Oligocene; Mio—Miocene; Pli—Pliocene.
Figure 1 in Aedeagus evolution promotes speciation? A primary pattern in rove beetle phylogeny
Figure 1. Bayesian phylogenetic tree for the partitioned combined analysis of four genes. Only posterior probabilities above 0.60 are shown. Colored branches represent the mainly monophyletic groups resolved in the phylogenetic inference. Verticle bars: thick bars denote the tribes of Staphylinini, thin bars the subtribes, grey bar the outgroup. The capital letters "A" and "B" refer to two main clades discussed in the text.
FIG. 4. Maximum-likelihood phylogeny for 45 in Phylogenetic Relationships of New World Porcupines (Rodentia, Erethizontidae): Implications for Taxonomy, Morphological Evolution, and Biogeography
FIG. 4. Maximum-likelihood phylogeny for 45 ingroup (erethizontid) terminals; outgroup taxa are not shown. Labeling conventions and nodal support statistics are the same as in figure 3. Capital letters (A, B, C) indicate unnamed clades discussed in the text.
FIG. 8. Mongolemys elegans, additional material. IGM 90 in New material of Mongolemys elegans Khosatzky and Mlynarski, 1971 (Testudines: Lindholmemydidae), from the Late Cretaceous of Mongolia with comments on bone histology and phylogeny
FIG. 8. Mongolemys elegans, additional material. IGM 90/30, small articulated shell: A–B, dorsal view; C–D, ventral view. IGM 90/22–23, one juvenile and one hatchling associated shells: E–F, dorsal view. IGM 90/31, nearly complete plastron of a juvenile: G–H, ventral view. IGM 90/51, complete carapace and caudal vertebrae series: I–J, ventral view. IGM 90/54, partial carapace showing the complete series of thoracic vertebrae: K–L, ventral view. IGM 90/41, complete right hyoplastron from a juvenile specimen: M, ventral view; N, dorsal view. Abbreviations: abs, axillary buttress scar; brg, bridge; cav, caudal vertebra. (See fig. 4 for remaining abbreviations).
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OpenNeuro
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