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Fig. 14 in A new species of Algon from Vietnam (Coleoptera: Staphylinidae: Staphylininae)
Fig. 14: Type locality of Algon fansipanicus. Photo: Paul Wunderle. Ƌ: sternite VIII (Fig. 9) with broadly V-shaped posterior excision; aedeagus (Figs 10-13) very long and slender, 2.1 mm long; median lobe apically bent and subapically dentate in lateral view, very acute in ventral view; paramere slender, apically not reaching apex of median lobe, much more slender than median lobe in ventral view, and with one peg-seta at some distance from the apex.
FIG. 14 in Mammalian Diversity And Matses Ethnomammalogy In Amazonian Peru Part 4: Bats
FIG. 14. Hsunycteris cf. thomasi feeding on a Chelonanthus alatus (Gentianaceae) at Jenaro Herrera. Photograph by Marco Tschapka.
FIG. 14. Astrapotherium magnum MACN A 8580 in Cranial Morphology And Phylogenetic Relationships Of Trigonostylops Wortmani, An Eocene South American Native Ungulate
FIG. 14. Astrapotherium magnum MACN A 8580, transverse segments through skull in rostrocaudal order, all to same scale. In A, B, continuous chambers related to massive frontal sinus expansion serve to isolate cranial cavity from skull's sidewalls (suggested by black arrows); C, successive segments through apparent right side, illustrating relationship of frontal sinus (1) to extratympanic aditus (2) and other chambers in retroarticular process (3); D, segment through fenestra vestibuli (4) and aditus of epitympanic sinus, fully prepared on right side (white arrow) but still blocked by matrix on left; E, F, segments through rear of tympanic cavity and foramen magnum, illustrating positions of temporal sinus, posttemporal canal, sulcus for?vertebral artery, lambdoidal process of petrosal, and paracondylar process (cf. Tetramerorhinus, fig. 40H). In B, C, white asterisks mark a large longitudinal conduit within cranial sidewall that corresponds, in other SANUs, to trackway of temporal sinus. But this feature also communicates with spaces that open into retroarticular process' aditus, indicating that both kinds of sinuses (pneumatic and venous) were housed in same bony chambers (see text).
FIG. 14 in Mammalian Diversity And Matses Ethnomammalogy In Amazonian Peru Part 3: Marsupials (Didelphimorphia)
FIG. 14. Ventral views of palates of A, Metachirus nudicaudatus (AMNH 266449) and B, M. myosuros (MUSM 15309) illustrating species divergence in size of the maxillopalatine fenestrae (mpf).
Figure 14 in A multivariate morphometric analysis and systematic review of Pseudonaja (Serpentes, Elapidae, Hydrophiinae)
Figure 14. Geographical distribution of Pseudonaja mengdeni specimens examined in this study (closed circles) and/or included in Skinner et al.'s (2005) phylogenetic analysis (open circles represent specimens not included in the morphometric analyses). Codes for geographical groups correspond with those in Table 2.
Figure 14 in Morphological evolution in Ceratophryinae frogs (Anura, Neobatrachia): the effects of heterochronic changes during larval development and metamorphosis
Figure 14. Presence and absence of m. suspensoriohyoideus among selected anuran tadpoles, following the criteria proposed by Haas (2003) at larval stage 37. A, Pseudis platensis. The muscle is absent. B–F, the muscle is present. B, Telmatobius atacamensis. C, Lepidobatrachus laevis. D, Lepidobatrachus llanensis. E, Ceratophrys cranwelli. F, Chacophrys pierottii. The absence of m. suspensoriohyoideus was reported for Ceratophrys ornata, L. laevis (Ruibal & Thomas, 1988; Haas, 2003), and C. cranwelli (Vera Candioti, 2005), but Palavecino (1999) described it in C. ornata and C. cranwelli. Haas (2003) proposed that the absence of m. suspensoriohyoideus is a synapomorphy for the Ceratophrys and Lepidobatrachus clade, and Frost et al. (2006) extended the synapomorphy for Ceratophryini. Our data demonstrate the presence of the m. suspensoriohyoideous in tadpoles of the three genera of Ceratophryinae. Abbreviations: oh, m. orbitohyoideus; sh, m. suspensoriohyoideus. Scale bars: 1 mm.
Figure 14 in European cave shrimp species (Decapoda: Caridea: Atyidae), redefined after a phylogenetic study; redefinition of some taxa, a new genus and four new Troglocaris species
Figure 14. Distribution and differerenciation of the subgenera Troglocaris (Spelaeocaris) and Troglocaris (Troglocaridella) (insert). Solid symbols represent the localities of the sequenced samples. Type localities of species: HER, Vjetrenica, for Troglocaris (Troglocaridella) hercegovinensis; KAP, Obajdinova pećina, for Troglocaris (Spelaeocaris) kapelana sp. nov.; NEG, Karišnica, for Troglocaris (Spelaeocaris) neglecta sp. nov.; PRA, Obod for Troglocaris (Spelaeocaris) prasence sp. nov.; PRE, Dejanova pećina, for Troglocaris (Spelaeocaris) pretneri; sp, Suvaja for T. (Spelaeocaris) sp. Dotted lines indicate the supposed smallest possible areas of the named taxa.
Figure 14. Distribution map. A in Systematics and phylogeny of Philautus Gistel, 1848 (Anura, Rhacophoridae) in the Western Ghats of India, with descriptions of 12 new species
Figure 14. Distribution map. A, Philautus bobingeri; B, Philautus bombayensis; C, map showing Travancore (shaded in grey), from which the type of Philautus chalazodes was collected; D, Philautus charius.
Figure 14 in Revision and cladistic analysis of Isoctenus and description of a new neotropical genus (Araneae, Ctenidae, Cteninae)
Figure 14. Isoctenus minusculus comb. nov.: A, male palp, ventral view; B, male palp, retrolateral view; C, epigynum, ventral view; D, epigynum dorsal view. Scale bars: 0.50 mm.
Figure 14 in A review of the New Zealand Chirostylidae (Anomura: Galatheoidea) with description of six new species from the Kermadec Islands
Figure 14. Uroptychus toka sp. nov., holotype, ♀ ovig., NMNZ Cr. 012090: A, carapace and abdomen, dorsal, setae omitted; B, carapace and abdomen, lateral, setae omitted; C, sternal plastron; D, telson, setae omitted; E, antenna, left, ventral; F, endopod of third maxilliped, left, lateral, setae omitted; G, right cheliped, dorsal; H–J, right pereopods 2–4; K, dactylus and distal portion of propodus of right pereopod 2, lateral. Scale bars = 2 mm.
Figure 14 in Craniodental anatomy of late Oligocene archaeohyracids (Notoungulata, Mammalia) from Bolivia and Argentina and new phylogenetic hypotheses
Figure 14. Archaeohyrax suniensis sp. nov., lower permanent cheek teeth. A, left p3-m2, SAL 311. B, right p3-m2 (reversed), SAL 309. C, left p3-m3, YPM-PU 22067 (partial). Labial to left and mesial at the top. Scale bar = 1 cm.
Figure 14 in Revision of the genus Bosmina Baird, 1845 (Cladocera: Bosminidae), based on evidence from male morphological characters and molecular phylogenies
Figure 14. Bosmina (Lunobosmina) oriens: juvenile female from a pond on highway 1, Newfoundland, Canada (A, C–F), and from Great Pond, Cape Cod, Massachusetts, USA (B); juvenile male II from Hell Hollow Pond, Connecticut, USA (G–M). A, B, general view of juvenile female; C, anterior view of juvenile female; D, antennular sensory setae and frontal head pore of juvenile female; E, lateral head pore of juvenile female; F, mucro of juvenile female; G, juvenile male II, general view; H, head of juvenile male II, anterior view; I, mucro of juvenile male II, inner view; J, postabdomen of juvenile male II; K, setae at coxal part of antenna II of juvenile male II; L, rudimentary sensory seta at distal segment of antenna II of juvenile male II; M, distal portion of limb I of juvenile male II. Scale bars: 100 Mm.
Figure 14 in First record of the taxon Echinopsyllus (Copepoda, Harpacticoida, Ancorabolidae) from the deep sea of Campos Basin, Brazil, with the description of three new species and their contribution to phylogenetic analysis
Figure 14. Echinopsyllus grohmannae sp. nov., female. A, A1; B, A2 (distal minute seta on the allobasis arrowed). Scale bar = 50 Mm.
Figure 14 in Devonian actinopterygian phylogeny and evolution based on a redescription of Stegotrachelus finlayi
Figure 14. Nuchal hump: A, specimen BMNH P.13418; B, specimen NMS G 2002.26.1384. Scale bars = 10 mm.
Figure 14 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 14. Cyphophthalmus gordani sp. nov. (holotype except B, F – female paratype). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 14 in Character-matrix based descriptions of two new nemertean (Nemertea) species
Figure 14. Schematic representation of the proboscis apparatus showing proboscis nerves. Abbreviations: P, proboscis; PN, proboscis nerves; PNS, peripheral neural sheath; R, rhynchocoel; SPN, secondary proboscis nerves.
Figures 6–14 in Revision of Tegyrius (Coleoptera: Chrysomelidae: Galerucinae: Alticini), with descriptions of eight new species
Figures 6–14. Tegyrius antennatus (Medvedev, 2001) (specimens from the Knuckles Range); 6, intercoxal ridges on the first abdominal ventrite; 7, male last abdominal ventrite; 8, aedeagus, ventral view; 9, aedeagus, lateral view; 10, distal opening; 11, tegmen; 12, spermatheca; 13, vaginal palpi; 14, tignum.
Figure 14 in Revision of the Helicellinae of Crete (Gastropoda: Hygromiidae)
Figure 14. Helicellinae from Crete: genitalia. Scale bar: 1 mm. A, Pseudoxerophila oertzeni (Maltzan, 1887), Omalos (ZMH 29719). B, Xeromunda candiota (L. Pfeiffer, 1849), Drapanos, 4 km towards Kokkinio Chorio (ZMH 36255). C, Xerotricha apicina (Lamarck, 1822), Corsica, Cardo (from Giusti & Manganelli, 1989: fig. 4B). D, Xerotricha conspurcata (Draparnaud, 1801), Sardinia, Valletta Logulentu (from Giusti & Manganelli, 1989: fig. 2B). E, Microxeromagna lowei (Potiez & Michaud, 1835), Greece, Lakonia, Sgardelianika near Neapoli (from Hausdorf, 1990b: fig. 1). F, Cernuella (Cernuella) virgata (Da Costa, 1778), Roustika, 0.2 km towards Rethimnon (ZMH 36110).
Figure 14 in Geometric approaches to the taxonomic analysis of centipede gonopods (Chilopoda: Scutigeromorpha)
Figure 14. Outline shape models of positions along the canonical variate axes (numbers in parentheses) shown in Figure 13 projected into the space of the extended eigenshapes. Outlines are overlain at the landmark from which digitization started in the figure to the right of each sequence in order to illustrate better the magnitudes and directions (arrows) or localized shape change. See text for discussion.
Figures 14–15 in A cladistic analysis of the Stygnicranainae Roewer, 1913 (Arachnida, Opiliones, Cranaidae) - where do longipalp cranaids belong?
Figures 14–15. Agathocranaus innocens sp. nov., male holotype (AMNH) from Ecuador. Habitus. Fig. 14. Dorsal view. Fig. 15. Lateral view. Scale bars = 3 mm.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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