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Figures 14–23. 14–21 Theridion manjithar Tikader, 1970 in A new species of the cob web spider genus Theridion from India (Araneae: Theridiidae)
Figures 14–23. 14–21 Theridion manjithar Tikader, 1970, holotype (NZC-ZSI-3275/18).14, abdomen, dorsal view. 15, same, anterior view. 16, same, posterior view. 17, same, ventral view. 18, carapace, dorsal view. 19, same, lateral view. 20, epigyne, dorsal view. 21, vulva, dorsal view. Scale bars 14-17, 0.5mm; 18-19, 0.2mm; 20-21, 1mm. 22–23 Theridion melanostictum O. Pickard-Cambridge, 1876. 22- internal epigyne, dorsal view. 23- vulva, dorsal view. Scale bars, 1mm.
Figsures 1‒14 in New data on Neotropical Carpenter-Moths of Subfamily Hypoptinae Neumoegen & Dyar, 1894 (Lepidoptera: Cossidae). I. New taxa with bifurcated uncus
Figsures 1‒14. Adult specimens of Hypoptinae, males: 1 ‒ Uretiana vicunensis, holotype: ♂ Chile, Vicuña, 606 m., Prov. de Coquimbo, 15-II-1936, E. Ureta coll. (Col. M. N. n. 2105); 2. U. vicunensis, ♂, Chile, Elqui, El Bosque - Hurtado, 17 September 1996 (GenPr-Heterocera MWM 37.007); 3. U. vicunensis, ♂ Brasil, Parana Curitiba, Serra Do Mar, Estrada De Castelhanos, March 1998, ca. 500m, leg H. Thöny; 4. U. tucumana, holotype: ♂ Argentina, prov. Tucuman (MLP); 5. U. infans, holotype: ♂ S Bernardino, Paraguay, K. Fiebrig collector, Nov., Type №41717 U.S.N.M. (USNM); 6. Dogniniya sterila holotype: ♂ Saint-Laurent-du-Maroni, Guyane française, Dognin Collection, Type №29892 U.S.N.M. (USNM); 7. D. beatrix, holotype: ♂ Quirigua, Guatemala, Schaus and Barnos coll., April, Type №23431 U.S.N.M. (USNM); 8. D. lemoulti, holotype: ♂ Uypiranga, Bresil, E. Le Moult 1933 (MNHN); 9. D. huanuco, holotype: ♂ Peru, prov. Huánuco, Yayapichis, ACP Panguana, 9°36″S / 74°56″W, September 2013, 220 m., leg. Hubert Thöny (MWM); 10. Qhichwaruna pennata, holotype: ♂ Argentinien, Cafayate, Prov. Catamarca, 16-11-98, Leg. A. Ugarte P. (MWM); 11. Wiraqucha huberti, holotype: ♂ Brasilien, Minas Gerais Poté, ca. 500m., 30.03.1996, Leg. Hubert Thöny (MWM); 12. W. equadorica, holotype: ♂ Ecuador oriente Napo Rte Cosanga-Tena PK 18 2.000 m., 4-VIII/90, J. Haxaire D. Herbin, (EC HAX 90 020), (MNHN); 13. Thonyocossus brasiliensis, holotype: ♂ Brasilien, Minas Gerais Poté, ca. 500m., 01.03.1996, Leg. Hubert Thöny (MWM); 14. Hastam gracilis, holotype: ♂ Brasilien, Esp. Santo, Santa Leopoldina, Boquerao, ca. 600m, 15.09.1997, leg. H. Thöny (MWM).
Figure 14 in New data on the butterflies of Western Stara Planina Mts (Bulgaria & Serbia) (Lepidoptera, Papilionoidea)
Figure 14. Distribution of Brenthis ino (Rottemburg, 1775) in Bulgaria. Species maps legend: empty circle – locality before 1980, empty circle with bold black margin – locality between 1980 to present article, black circle – new records.
Figure 14 in Three new genera and four new species of katydids (Orthoptera: Tettigoniidae) from Cuba and Hispaniola, Greater Antilles
Figure 14. Adult male holotype (a–c) and adult female paratype (d–f) of Anacaona bellatrix n. gen., n. sp., respectively, close-up views: a) apex of abdomen, dorsal; b) apex of abdomen, ventral; c) apex of abdomen, posterior; d) apex of abdomen, dorsal; e) apex of abdomen, ventral; f) ovipositor, lateral.
Figure 14-II in Review of genera Evarcha and Nigorella, with comments on Emertonius, Padilothorax, Stagetillus, and description of five new genera and two new species (Araneae: Salticidae) *
Figure 14-II. Diagnostic characters of species of the genus Evawes. A - Evawes madagascariensis, B - Evawes zimbabwensis, C - Evawes longula, D -Evawes denticulata, E - Evawes maculata, F - Evarcha bicuspidata, G -Evawes mirabilis, H - Evawes pinguis, I-J –Evawes awashi, K-L –Evawes prosimilis.
Fig. 14 in Revision of the genus Dellia Stål, 1878 (Orthoptera: Acrididae). Part 1. Two redescriptions and seven new species from Cuba
Fig. 14. Adult male holotype of Dellia siboney n. sp., full-body views: a) dorsal; b) lateral; c) ventral. Scale bar in millimeters. Coloration after two days of alcoholic preservation.
Figure 14 in Taxonomic survey of the genera Euophrys, Pseudeuophrys and Talavera, with description of Euochin gen. n. (Araneae: Salticidae) and with proposals of a new research protocol*
Figure 14. Diversity of diagnostic characters in Euophrys (part IV). A - Euophrys cochlea, B - E. convergentis, C - E. dhaulagirica, D - E. declivis, E - E. nangqianensis, F - E. everestensis, G - E. omnisuperstes, H-I - E. yulungensis. SOURCES: A - Wesolowska, Azarkina & Russell-Smith (2014) Zootaxa 3789(1) 12, f. 18-33, B - Denis (1937b) Proceedings of the Zoological Society of London 1936:: 1054, pl. 5, f. 6, C, H, I - Żabka (1980b) Senckenbergiana Biologica 60 365, f. 13-14; 363, f. 12, D - Prószyński (2009b) Arthropoda Selecta 18: 160, f. 32-33, E - Hu (2001) Henan Science and Technology Publishing House 383, f. 239.1-3, F-G -Wanless (1975) Bulletin of the British Arachnological Society 3(5) 134, f. 4-5, 9-11; 132, f. 1-3, 6-8. All ©copyrights are retained by the original authors and copyright holders, used by their courtesy.
Fig. 14 in Moles (Talpidae) from the late Middle Miocene of South Germany
Fig. 14. Desmanodon sp., Petersbuch 10. A. Right dentary fragment with p2–p3, NHMA P10−618/3, occlusal view; ca. × 15. B. Left dentary fragment with p4–m1, NHMA P10−618/1, occlusal view; ca. × 15. C. Right P4, NHMA P10−618/4, occlusal view; ca. × 15. D. Left humerus, NHMA P10−619/1, anterior view; ca. × 7.5. E. Right humerus, NHMA P10−619/2, posterior view; ca. × 7.5.
Fig. 14. Pachysolenia cylindrica Cuif, 1975 in Three-dimensional micro- and nanostructural characteristics of the scleractinian coral skeleton: A biocalcification proxy
Fig. 14. Pachysolenia cylindrica Cuif, 1975, ZPALH. XXI/4. Triassic, Lower Norian. Alakir Çay,Turkey. A–C. Complementary regions of transversely sectioned and polished pachytheca: TLM image (A), greyscale Sr (B) and Mg (C) mapping acquired on the electron microprobe by wavelength−dispersive techniques; darker areas equal very low concentration whereas lighter areas equal slightly higher concentrations. Sr (in B) shows enrichment, at least in some regions (arrows) where Mg (in C) appears depleted. Sr mapping of diagenetically non−altered fibrous parts of coralla of extant corals (not illustrated here) invariably shows nearly homogenous distribution of this element. D. TLM view of longitudinally sectioned pachytheca and septum; part of the preserved septum encircled and enlarged in E to show "non−trabecular" nature of dRAF. F. Transverse polished section of pachytheca in TLM; fibers show faint regular 5–8 µm alternations of lighter and darker zones. G. Homogenous septal dRAF zone in SEM view of transversely polished and etched section. H. Transverse polished and etched section of pachytheca (SEM); fibrous skeleton shows negative and positive etching relief (at ca. 5–8 µm distance).
Figura 14 in Tarántulas chilenas de la subfamilia Theraphosinae (Mygalomorphae: Theraphosidae): una revisión a nivel de género
Figura 14. Mapa de distribución. a. Mapa de las especies de Euathlus presentes en Chile. b. Mapa de las especies de Grammostola presentes en Chile. Regiones de Chile: AN= Antofagasta; AT= Atacama; CO= Coquimbo; VA= Valparaíso; ME= Metropolitana; OH= O'Higgins; MA= Maule; ÑU= Ñuble; BI= Biobío; AR= Araucanía. / Figure 14. Distribution map. a. Map of Euathlus species present in Chile. b. Map of Grammostola species present in Chile. Regions of Chile: AN= Antofagasta; AT= Atacama; CO= Coquimbo; VA= Valparaíso; ME= Metropolitana; OH= O'Higgins; MA= Maule; ÑU= Ñuble; BI= Biobío; AR= Araucanía.
Fig. 14 in The endocranium of the theropod dinosaur Ceratosaurus studied with computed tomography
Fig. 14. Ceratosaurus magnicornis (MWC 1, Fruita, Colorado, Morrison Formation, Upper Jurassic). Summary three−dimensional digital reconstruction featuring the skull overlay in grey, endocranium in violet, inner ear in yellow, pneumatic sinuses in light blue, and venous sinuses in red, in right lateral (A) and dorsal (B) views.
Fig. 14 in Late Miocene large mammals from Yulafli, Thrace region, Turkey, and their biogeographic implications
Fig. 14. Map (slightly modified from Vasiliev et al. 2004) of the Tethys (dark grey) and Paratethys (light grey) region in early late Miocene times, showing the main mammalian localities with and without Dorcatherium, and the tentative extent of the provinces discussed in the text. 1, North−Western Province; 2, North−Dacian Province; 3, Balkano−Iranian (= Sub−Paratethyan) Province; 4, Greek Macedonian Province; 5, Eastern Aegean Province; 6, Anatolian Province.
Figures 12–14 in A new species of Ptiloglossa from Mexico, with new records of Ptiloglossa cyaniventris from Panama and Costa Rica (Hymenoptera: Colletidae)
Figures 12–14. Male terminalia of Ptiloglossa cyaniventris Friese from Panama. 12. Metasomal sternum VII. 13. Metasomal sternum VIII. 14. Ventral view of genital capsule.
Fig. 14 in Post-extinction brachiopod faunas from the Late Permian Wuchiapingian coal series of South China
Fig. 14. Cardinal process of Chengxianoproductus cf. changxingensis Liao and Meng, 1986 (based on specimen NMV P309640).
Fig. 14 in New teeth of allotherian mammals from the English Bathonian, including the earliest multituberculates
Fig. 14. Diagrams to illustrate postulated evolution of occlusion. A–E. Divergence between Allotheria and Mammaliaformes. The teeth are seen mesiodistally, buccal to the left. Arrows indicate direction of the power stroke. A. Plesiomorphic condition, e.g., Sinoconodon, with no occlusal contact. B, C. Opposition develops by formation of supplementary cusprows in Allotheria; B is a hypothetical transitional stage. D. Unilateral transverse shearing in morganucodonts. E. Rearrangement (triangulation) of cusps, as in symmetrodonts, resulting in mesially and distally facing wear facets. F–I. Allotherians illustrating stages in the evolution of palinal occlusion. Teeth seen in side view, distal to the left. F. Vertical crushing in Theroteinus. G. Distally oblique crushing in Millsodon. H. Basin grinding with palinal movement in Thomasia. I. Horizontal palinal grinding in multituberculates.
Figure 14. - Relationship between measurements M1 and M2 in Guide for the identification of archaeological sea sturgeon (Acipenser sturio and A. oxyrinchus) remains
Figure 14. - Relationship between measurements M1 and M2 on palatopterygoid from modern sturgeons of known length (adapt- ed from Desse-Berset, 1994). ● Data for modern A. sturio from Desse-Berset, 1994; O RBINS 24792, A. oxyrinchus; Θ BAI 1884, morphologically identified A. sturio.
Fig. 14 in Nanostructure of biogenic versus abiogenic calcium carbonate crystals
Fig. 14. Thermograms showing direct thermogravimetrical (TG; milligrams), differential thermogravimetrical (DTG; arbitrary units), and differential thermo−analytical (DTA; arbitrary units) curves of synthethic aragonite (A) and three samples with two different nanostructural patterns: Triassic Pachysolenia cylindrica (B) without distinct nanograins; Jurassic Isastraea cf. bernensis (C) and Recent Favia stelligera (C) with well developed nanograins. Assumed amount of intraskeletal hydrated organic components was calculated based on distinct weight loss of 400 mg sample that occurred at ca. 300–450°C.
Fig. 14 in Early Frasnian acanthodians from central Iran
Fig. 14. Photomicrographs of histological structure of?ischnacanthiform tooth whorl (A) and dentigerous jaw bones (B, C) in vertical longitudinal sections. Early Frasnian, horizon GI4 of an unnamed formation in the Chahriseh section, Kaftari Mt., central Iran. A. Thin section LIGG 3810 of a whorl with randomly displaced anterior tooth cusps of different size (left part in A1) and an axial line of three larger cusps behind. A1, high vascularisation of odontocytic mesodentine or bone tissue composing most of whorl; lamellar bone filling only thin basal plate; A2, appearance of denteons (light strips surrounding dark vascular canals) and densely concentrated polygonal odontocyte cells characteristic of mesodentine/osteodentine in the intervascular space exposed in a central area of the same whorl, at higher magnification. B. Thin section LIGG 3813 of a single tooth cusp with the jaw bone portion from the presumed first type of jaw fragment showing general structure of tissues, with dentine canals in syncitial mesodentine of a cusp superficially grading to odontocytic mesodentine in a deeper layer (B1), at higher magnification (B2), and pulp canals with branching dentine tubules in odontocytic mesodentine which covers the basal osseous layer of the central cusp (B3) (place indicated by rectangle in B1). C. Thin section LIGG 3814 of a single tooth from the lingual row on a portion of jaw bone of the second type. The odontocytic mesodentine with large vascular canals extends to the cusp apex (C1), grading into a cellular bone more deeply with increased density of osteocyte cells and wider vascular canals surrounded by thin osteons (magnified basal part of jaw bone, C2). Scale bars 0.1 mm.
Fig. 14 in Reconstruction of Oligocene and Neogene freshwater fish faunas-an actualistic study on cypriniform otoliths
Fig. 14. Utricular otoliths (lapilli) of Recent Leucaspius delineatus (Heckel, 1843) from breeding stations in Germany. A. BSPG 2003 IV 63b in dorsal view, represented as right lapillus, and mirrored (A1) and in anterior view, represented as left lapillus (A2). B. BSPG 2003 IV 63a in ventral view, represented as left lapillus (mirrored). C. BSPG 2003 IV 62 in dorsal view, represented as right lapillus (mirrored). A, B display a lapilli pair. SEM−pictures (A, B), digital picture (C).
Fig. 14 in A revision of the simplex species group of the cleptoparasitic bee genus Triepeolus Robertson, 1901 (Hymenoptera: Apidae)
Fig. 14. Triepeolus apache sp. nov. A, D. Holotype, ♀ (BOLD sample ID: CCDB-24584 D03; PCYU). A. Habitus, lateral view. B. Paratype, ♀ (AMNH), habitus, dorsal view. C. Allotype, ♂ (BOLD sample ID: CCDB-38770 C03; RSKM PCYU:AZ09:40/RSKM_ENT_E-125505), habitus, lateral view. D. Pseudopygidial area, dorsal view.
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