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Fig. 16 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 16. Magnified views (×100) of plastic impressions of hair shafts in the outgroup taxon Mormoops and two phyllostomids. The detail of the basal bulb is at 430× magnification and represents a ''typical basal bulb'' (Benedict, 1957: plate 24l) of the kind found in Desmodus (the drawing is of Rhinolophus). Note the ''alternate annular'' arrangement of the scales in Lonchorhina (see character 3; drawn after Benedict, 1957: plates 24l, 29v, 30a, v).
Fig. 34 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 34. Dorsal surface of the tongue in selected phyllostomids. Lowest inset is of a lateral circumvallate papilla. A. Phyllostomus hastatus (AMNH 233176). Upper inset: basketlike papilla. B. Uroderma bilobatum (AMNH 171294). C. Ametrida centurio (AMNH 247645). Scale bar = 2 mm.
Fig. 11 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 11. Consensus tree from Honeycutt and Sarich (1987a; redrawn from fig. 3) based on immunological, chromosomal, and morphological data.
Fig. 12. A in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 12. A. Hypothesis of stenodermatine generic relationships proposed by Owen (1987) based on his study of continuous and discrete craniodental and external characters (redrawn from Owen, 1987: fig. 17). B. Result of Owen's (1991; redrawn from fig. 1) study designed to clarify relationships among Dermanura, Enchisthenes, and Koopmania, which was based on a reanalysis of selected characters from Owen (1987). C. Lim's (1993; redrawn from fig. 6) ''working hypothesis'' of stenodermatine relationships using discrete craniodental and external characters. Note that Artibeus includes Dermanura, Enchisthenes, and Koopmania. D. Lim's (1993; redrawn after fig. 3) reanalysis of Owen's (1991) data set.
Fig. 8 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 8. Hood and Smith's (1982; redrawn from fig. 5) hypothesis of higherlevel relationships among phyllostomid bats based on morphology of the female reproductive tract.
Fig. 42 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 42. Diagramatic dorsal view (left) and longitudinal section of one hemisphere (right) of the chiropteran brain illustrating the progressive coverage of the median longitudinal fissure and inferior colliculi (ic). A. Complete exposure of the median longitudinal fissure and inferior colliculi. B. Partial coverage of both the fissure and inferior colliculi. C. Complete coverage of the fissure and colliculi Note that the cerebellar vermis covers the inferior colliculi, but the relationship of the inferior colliculi to each other does not change (redrawn from Schober and Brauer, 1974: fig. 99)
Fig. 9 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 9. Pierson's (1986; redrawn after fig. 35) proposed phylogeny of phyllostomid relationships based on transferrin immunology. This tree does not include all the taxa used by Pierson (1986) see the text for discussion of additional relationships. Asterisks indicate taxa for which antisera were unavailable.
Fig. 14 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 14. Gimenez (1993) used the topology of Baker et al. (1989) to partition her analyses of lingual morphology. A. Cladogram of relationships from Gimenez's (1993; redrawn from fig. 22) analysis of desmodontines, vampyrines, Macrotus, Micronycteris, and Phyllostominae. B. Gimenez's (1993; redrawn from fig. 24) proposed relationships among Stenodermatini genera. C. Gimenez's (1993; redrawn from fig. 25) proposed relationships among Glossophagini genera.
Fig. 7. A in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 7. A. Griffiths' (1982; redrawn from fig. 33) hypothesis of relationships among nectarfeeding phyllostomids based on hyoid and lingual data and additional consideration of karyological and dental data. The open base of the cladogram signifys the possible relationship of the lonchophylline clade to other nonnectarfeeding phyllostomids. Asterisks indicate taxa whose placement was based soley on craniodental data. B. Haiduk and Baker's (1982; redrawn from fig. 8) tree depicting relationships among nectarfeeding phyllostomids based on Gbanded chromosome morphology. C. Haiduk and Baker's (1982; redrawn from fig. 9) reanalysis of Griffiths' (1982) original data, without consideration of char
Fig. 25 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 25. Ventral view of the basicranium in A. Glossophaga soricina and B. Choeroniscus intermedius. The difference in inflation of the pterygoids is indicated by the arrows. Redrawn from Phillips (1971: fig. 45).
Fig. 19 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 19. Anterior view of the noseleaf in A. Desmodus rotundus (AMNH 267503). B. Vampyrum spectrum (AMNH 202292). C. Phyllostomus hastatus (AMNH 233176). Scale bar = 5 mm.
Fig. 5 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 5. ''Tentative'' phylogeny proposed by Smith (1976; redrawn from fig. 2) after an evaluation of previously published data including dental, immunological, karyological, parasitological, and postcranial data. Asterisk indicates an extinct taxon.
Fig. 10 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 10. Honeycutt's (1981; redrawn after fig 2) and Honeycutt and Sarich's (1987a; redrawn after fig. 1) tree based on bidirectional immunological comparisons of albumins. The authors fit other taxa into this tree using unidirectional comparisons; placement of these taxa is described in the text.
Fig. 37 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 37. Dorsal (left) and lateral (right) views of the tongues of representative species with hairlike papillae. Insets feature closeups of individual hairlike papillae. A. Glossophaga soricina (AMNH 237911). B. Lonchophylla thomasi (AMNH 267452). C. Phyllonycteris poeyi (AMNH 236698). Scale bar = 2 mm.
Fig. 17 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 17. Lateral view of the head (left) and ventral view of the chin (right) of selected taxa illustrating the position and number of vibrissae found in clusters. A. Generalized mammal (after Brown 1971: fig. 6) B. Desmodus rotundus (AMNH 267503). C. Micronycteris megalotis (AMNH 267411) D. Lonchophylla thomasi (AMNH 266107). E. Uroderma bilobatum (AMNH 268564). F. Noctilio leporinus (AMNH 267408). Scale bar = 10 mm.
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.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.