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72 results for “Raphitomidae”
Figure 10 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 10. Shells of Mioawateria species. (A) Mioawateria personata (Powell, 1942) holotype Institute of Geological and Nuclear Sciences Limited (GNS) TM3761; (B) Mioawateria blakeana (Dall, 1881) comb. n., Smithsonian National Museum of Natural History (USNM) 87427; (C) Mioawateria brachis (Dall, 1919) comb. n., holotype USNM 96486; (D) Mioawateria isogonia (Dall, 1908) comb. n., holotype USNM 123112. Scale bar = 3 mm.
Figure 9 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 9. Shells of deep-sea raphitomid species previously assigned to Gymnobela. (A) Spergo africana (Sysoev, 1996) comb. n., holotype Natural History Museum of the United Kingdom (NHMUK) 1993114; (B) Spergo bululi (Stahlschmidt, Poppe and Tagaro, 2018) comb. n., holotype Muséum National d'Histoire Naturelle (MNHN) IM-2000-30,406; (C) Spergo oculifera (Kantor and Sysoev, 1986) comb. n., holotype Zoological Museum of Moscow University (ZMMU) Lc 22338; (D) Austrobela fulvotincta (Dautzenberg and Fischer, 1896) comb. n., syntype Musée océanographique de Monaco (MOM) INV-18461; (E) Theta chrysopelex (Barnard, 1963) comb. n., holotype Iziko South African Museum ISAM A9857; (F) Theta homeotata (Watson, 1886) comb. n., holotype NHMUK 1887.2.9.1115; (G) Austrobela gypsata (Watson, 1881) comb. n., syntype NHMUK 1887.2.9.979–80; (H) Theta latistriata (Kantor and Sysoev, 1986) comb. n., holotype ZMMU Lc 22341. Scale bar = 10 mm.
Figure 8 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 8. Shells of Gymnobela species vouchers. (A) G. bairdii (Verrill and Smith, 1884), syntype Smithsonian National Museum of Natural History (UNSM) 37824; (B) G. rotundata Sysoev, 1990, holotype Zoological Museum of Moscow University (ZMMU) Lc 5718; (C) G. abyssorum (Locard, 1897), lectotype Muséum National d'Histoire Naturelle (MNHN) IM-2000-2750; (D) G. chyta (Watson, 1881), holotype Natural History Museum of the United Kingdom (NHMUK) 1887.2.9.1108; (E) G. granulisculpturata Sysoev, 1990, holotype ZMMU Lc 5725; (F) G. verecunda (Barnard, 1963), lectotype ISAM A9697; (G) G. mitrodeta Sysoev, 1997, holotype MNHN IM-2000-3121; (H) G. laticaudata Sysoev, 1990, holotype ZMMU Lc 5735; (I) G. engonia figured in Bouchet and Warén 1980 (fig. 123). Scale bar: A, C, F–G, I = 10 mm; B, H = 3.3 mm; D–E = 5 mm.
Figure 4 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 4. Shells of Gymnobela primary species hypotheses (PSHs)/species studied herein. (A) G. frielei (Verril, 1885), holotype Smithsonian National Museum of Natural History (USNM) 44653; (B) G4/ G. frielei Australian Museum (AMS) C.571666; (C) G4/G. frielei AMS C.571702; (D) G4/G. frielei AMS C.482314; (E) G4/G. frielei AMS C.571812; (F) G4/G. frielei AMS C.571677; (G) G4/G. glaucocreas (Barnard, 1963), holotype Iziko South African Museum (ISAM) A9821; (H) G3/G. angulosa Sysoev, 1988, holotype Zoological Museum of Moscow University (ZMMU) Lc-22363 (I) G3/G. angulosa AMS C.571649; (J) G3/ G. angulosa AMS C.571648; (K) G3/G. angulosa, Bavarian State Collection of Zoology (ZSM) mol 20070770. Scale bar = 10 mm.
Figure 2 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 2. Maximum likelihood (ML, left) tree and Bayesian consensus phylogram (BI, right) based on analyses of the concatenated sequence dataset. Numbers above branches indicate nodal support by Bayesian posterior probabilities (BPP) and ML bootstrap (BS). BPP values of 1 and BS values of 100% are represented by asterisks. Sequences of samples collected outside Australian waters are underlined. Samples whose shells are figured (scale bar = 10 mm) are in bold. The shell image of P1 has been digitally edited (grey area) to simulate an intact spire. Vertical bars mark distinct primary species hypotheses (PSHs) as delimited by the Automatic Barcode Gap Discovery (ABGD) method.
Figure 7 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 7. Bathymetric ranges of taxa studied herein as inferred from museum records of sequenced specimens. Primary species hypotheses (PSHs)/species represented by a single record are indicated with a circle.
Figure 1 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 1. Distribution of taxa studied herein in Australian waters. Numbers and letters in shapes indicate primary species hypotheses (PSHs)/species of: Gymnobela [circles: 1 – G1/ G. agassizi (Verrill and Smith, 1880); 2 – G2/G. engonia (Verrill, 1884); 3 – G3/G. angulosa Sysoev, 1988; 4 – G4/G. frielei (Verril, 1885)] and Pontiothauma (squares: 1 – P1/P. sp.; 2 – P2/ P. transregna sp. n.). Thin lines mark limits among marine realms (numbered as in Costello et al. 2017). Asterisks mark non-sequenced material. Scale bars = 200 km.
Figure 3 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 3. Shells of Gymnobela primary species hypotheses (PSHs)/species studied herein. (A) G1/ G. agassizi (Verrill and Smith, 1880), Australian Museum (AMS) C.519355; (B) G. agassizii (Verrill and S. Smith, 1880), holotype UNSM 37828; (C) G. engonia (Verrill, 1884), holotype Smithsonian National Museum of Natural History (USNM) 3483; (D) G2/G. engonia AMS C.594980; (E) G2/G. engonia AMS C.593510; (F) G2/G. engonia AMS C.482287; (G) G2/G. engonia AMS C.482286; (H) G2/G. engonia AMS C.571816. Scale bar: A–D, F–H = 10 mm; E = 5 mm.
Figure 6 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 6. Hypodermic teeth of primary species hypotheses (PSHs)/species studied herein. (A) G1/ Gymnobela agassizi (Verrill and Smith, 1880), Australian Museum (AMS) C.519355; (B) G2/Gymnobela engonia, AMS C.482287; (C) G3/Gymnobela angulosa Sysoev, 1988, Bavarian State Collection of Zoology (ZSM) mol 20070770; (D) G3/Gymnobela angulosa Sysoev, 1988 AMS C.571648; (E) G4/ Gymnobela frielei (Barnard, 1963) AMS C.482314; (F) P1/Pontiothauma sp. AMS C.482298; (G) P2/ Pontiothauma transregna sp. n. paratype AMS C.519398. Scale bar: A–E = 50 µm; F–G = 100 µm.
Figure 5 in Integrative taxonomy of Gymnobela and Pontiothauma (Conoidea: Raphitomidae) from Australian waters provides more evidence of transoceanic distribution in deep-sea gastropods
Figure 5. Shells of Pontiothauma primary species hypotheses (PSHs)/species. (A) P1/ P. sp. AMS C.519343; (B) P1/ P. sp. Australian Museum (AMS) C.571758; (C) P1/ P. sp. AMS C.482298; (D) P1/ P. sp. AMS C.519375; (E) P2/ P. transregna sp. n. holotype AMS C.571641; (F) P2/ P. transregna sp. n. paratype AMS C.519398; (G) P2/ P. transregna sp. n. paratype AMS C.593511; (H) P2/ P. transregna sp. n. paratype AMS C.482289; (I) P. mirabile holotype E.A. Smith 1895 Zoological Survey of India (ZSI) M179/1; (J) P. pacei E.A. Smith 1906 paratype Natural History Museum of the United Kingdom (NHMUK) 1906.7.21.1; (K) P. sp. AMS C.547959; (L) Miniatures of shells drawn to scale. Scale bars = 10 mm.
FIG. 14 in Three new species of Raphitoma Bellardi, 1847 (Mollusca, Gastropoda, Raphitomidae) from Croatian waters (NE Adriatic Sea)
FIG. 14. — Murex echinatus Brocchi, 1814: A, paralectotype, MCSNM i5429, 6.67 mm; B, box of types; C, probable Brocchi's original label; D, E, museum labels; F, label written by Rossi Ronchetti. Scale bar: 3 mm. Photos courtesy: Michele Zilioli (MCSNM).
FIG. 9 in Three new species of Raphitoma Bellardi, 1847 (Mollusca, Gastropoda, Raphitomidae) from Croatian waters (NE Adriatic Sea)
FIG. 9. — Raphitoma pusaterii Prkić & Giannuzzi-Savelli n. sp., Mljet Island (coll. RGS, h = 3.46 mm): frontal view of shell (A); apical (B), frontal (D) and dorsal (E) view of protoconch; detail of microgranules and transition from protoconch to teleoconch (C). Scale bars: A, 1 mm; B-E, 200 µm.
FIG. 17 in Three new species of Raphitoma Bellardi, 1847 (Mollusca, Gastropoda, Raphitomidae) from Croatian waters (NE Adriatic Sea)
FIG. 17. — Live specimen of Raphitoma echinatasensu Auctores - morphotype 2, Sevid, Croatia, depth 5 m, 18.3 mm.
FIG. 8 in Revision of Mediterranean and NE Atlantic Raphitomidae (Gastropoda, Conoidea) 8: The genus Leufroyia Monterosato, 1884
FIG. 8. — Leufroyia leufroyi (Michaud, 1828). Murter Island (Croatia), 3 m, h. 7.85 mm. A, Frontal view of shell; B-D, apical (B), frontal (D) and dorsal (C) view of protoconch. Scale bars: 2 mm (A), 300 µm (B-D).
FIG. 13 in Revision of Mediterranean and NE Atlantic Raphitomidae (Gastropoda, Conoidea) 8: The genus Leufroyia Monterosato, 1884
FIG. 13. — Leufroyia concinna (Scacchi, 1836). Dugi Otok Island (Croatia), 32-40 m, h. 10.53 mm. A, Frontal view of shell. B-D, apical (B), frontal (D) and dorsal (C) view of protoconch. Scale bars: 2 mm (A), 300 µm (B-D).
FIG. 21. — A in Revision of Mediterranean and NE Atlantic Raphitomidae (Gastropoda, Conoidea) 8: The genus Leufroyia Monterosato, 1884
FIG. 21. — A, Pleurotoma inflata De Cristofori & Jan, 1832, Lectotype, (MCSNM i 4296) Tabiano (Parma) Piacentian (Pliocene), h. 15.3 mm (after Pinna & Spezia, 1978, pl. 40); B, P. inflata, Ficarazzi (Palermo) (Lower Pleistocene), h. 18.9 mm (NMW, 12930), erroneously identified by Monterosato as Leufroyia volutella; C, P. inflata, Monte Pellegrino (Palermo) (Plio-Pleistocene) (MCZR-M-16706), h. 23.9 mm; D, Pleurotoma volutella Kiener, 1839, original drawings by Kiener, h. 25.4 mm; E, P. volutella, Ficarazzi (Palermo) (Lower Pleistocene), h. 21.5 mm; F, Pleurotoma cf. volutella Monte Pellegrino (Palermo) (Pliocene), h. 25.8 mm.
FIG. 18 in Revision of Mediterranean and NE Atlantic Raphitomidae (Gastropoda, Conoidea) 8: The genus Leufroyia Monterosato, 1884
FIG. 18. — Leufroyia villaria (Pusateri & Giannuzzi-Savelli, 2008): A, Mljet Island (Croatia) -70-100 m, amidst red coral colonies, h. 12.22 mm; B, Saronic Gulf (Greece), h. 16.1 mm; C, Saronic Gulf (Greece), h. 18.3 mm; D, South Eastern Sicily (Italy), h. 13.1 mm; E, Mljet Island (Croatia) 70-100 m, amidst red coral colonies, h. 11.5 mm; F, Lastovo Island (Croatia) 200 m, h. 16.7 mm; G, Mljet Island (Croatia) 70-100 m, amidst red coral colonies, h. 8.1 mm. Photo courtesy: B, C, Costas Kontadakis; D, Roberto Ardovini; F, Pero Ugarković.
FIG. 17 in Revision of Mediterranean and NE Atlantic Raphitomidae (Gastropoda, Conoidea) 8: The genus Leufroyia Monterosato, 1884
FIG. 17. — Leufroyia villaria (Pusateri & Giannuzzi-Savelli, 2008): A, holotype (MNHN-IM-2000-27244), Taormina (Italy) -15 m, h. 17.3 mm; B, paratype C (GOR), Capraia Island (Italy) 150 m, h. 16.9 mm; C, paratype A (MNHN-IM-2000-23353), Ras il-Wahx (Malta), 80-100 m, h. 11.5 mm; D, East Sicily (Italy), h. 12.4 mm; E, Porto Cesareo (Taranto - Italy), h. 14.2 mm; F, Fomm Ir-Riħ (Malta) 140 m, h. 10.76 mm; G, Ionian coasts of Calabria (Italy), h. 13.7 mm; H, Gorée (Senegal) (MNHN, Knudsen coll.), h. 11.4 mm; I, Mljet Island (Croatia), 70-100 m, amidst red coral colonies, h. 10.62 mm; J, Mljet Island (Croatia), 70-100 m, amidst red coral colonies, h. 8.58 mm; K, Saronikos Gulf (Greece), h. 17.1 mm; L, Saronikos Gulf (Greece), h. 16.6 mm. Photo courtesy: D, G, Roberto Ardovini; K, L, Costas Kontadakis.
FIG. 15 in Revision of Mediterranean and NE Atlantic Raphitomidae (Gastropoda, Conoidea) 8: The genus Leufroyia Monterosato, 1884
FIG. 15. — Leufroyia erronea Monterosato, 1884. A, Syntype, Shetland Islands (USNM 190581 ex Jeffreys coll.), h. 14.8 mm; B, Shetland Islands (USNM 190582 ex Jeffreys coll.), h. 14.5 mm; C, Shetland Islands (USNM 190578 ex Jeffreys coll.), h. 19.4 mm; D, Galicia (Spain), h. 16.2 mm; E, Mljet Island (Croatia), 70-100 m, amidst red coral colonies, h. 9.1 mm; F, Mljet Island (Croatia), 70-100 m, amidst red coral colonies, h. 8.3 mm; G, Mljet Island (Croatia), 70-100 m, amidst red coral colonies, h. 5.3 mm; H, Saronic Gulf (Greece), h. 6.15 mm - scale bar 200 µm. I, Pleurotomella demosia (Dautzenberg & Fischer, 1896), Açores (MNHN), 1300 m, 38°33'21"N, 30°28'54" W, h. 7.3 mm. Photo courtesy: A-C, Jolanda Villacampa (USNM); H, Costas Kontadakis.
FIG. 14 in Revision of Mediterranean and NE Atlantic Raphitomidae (Gastropoda, Conoidea) 8: The genus Leufroyia Monterosato, 1884
FIG. 14. — Leufroyia erronea Monterosato, 1884: A, Sardinia (Italy), h. 15.8 mm, with original labels by Tiberi and Monterosato; B, sine loco, h. 10.5 mm; C, Gorgona Island (Italy), h. 12.5 mm; D, Spain, h. 24 mm; E, Capraia Island (Italy) 120 m, h. 27 mm; F, Latium (Italy), h. 15.5 mm; G, Capo Corso (Italy), h. 8.5 mm; H, Mljet Island (Croatia) 70-100 m, h. 10.6 mm; I, Mljet Island (Croatia) 70-100 m, h. 15.7 mm. Photo courtesy: D, Peter Stahlschmidt, E, Enzo Campani, H, Morena Tisselli.
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