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FIGURE 35 A1–A2 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 35 A1–A2. Perrona lydiae (Hoernes & Auinger, 1891), lectotype, NHMW 1949/0005/0112a, Gainfarn (Austria). B1–B3. Perrona lydiae (Hoernes & Auinger, 1891), NHMW 1846/0037/0333, Enzesfeld (Austria). C1–C3. Perrona lydiae (Hoernes & Auinger, 1891), NHMW 1851/0006/0014a, Bad Vöslau (Austria). D1–D3. Perrona lydiae (Hoernes & Auinger, 1891), NHMW 1851/0006/0014b, Bad Vöslau (Austria). E1–E3. Perrona eleonorae (Hoernes & Auinger, 1891), paralectotype, NHMW 1846/0037/0309b, Enzesfeld (Austria). F1–F2. Perrona eleonorae (Hoernes & Auinger, 1891), paralectotype, NHMW 1847/0037/0310, Enzesfeld (Austria). G. Perrona herculea (Mayer-Eymar, 1886), S 1523, lectotype, Grund (Austria), ETH Zürich (Switzerland).
FIGURE 6 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 6. Apertures of Paratethyan Clavatulidae (C. = Clavatula, 'C.' = 'Clavatula', G. = Granulatocincta, M. = Megaclavaltula, O. = Olegia).
FIGURE 38 A1–A3 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 38 A1–A3. Perrona ernae (Šuklje, 1929), NHMW 2021/0156/0001, Weinsteig (Austria). B1–B2. Perrona ernae (Šuklje, 1929), lectoytpe. Inv. No. 6582-153/1,; Zaprešić-Brijeg at Samobor (Croatia). C1–C3. Perrona ernae (Šuklje, 1929), NHMW 1859/0045/0009, Kleinebersdorf (Austria). D1–D3. Perrona rosaliae (Hoernes & Auinger 1891), paralectotype, NHMW A1382, Enzesfeld (Austria). E1–E3. Perrona rosaliae (Hoernes & Auinger 1891), lectotype, NHMW 1999z0098/0002a, Vienna/ Pötzleinsdorf (Austria). F1–F3. Perrona rosaliae (Hoernes & Auinger 1891), paralectotype, NHMW 1999z0098/0002b, Vienna/ Pötzleinsdorf (Austria).
FIGURE 23 A1–A3 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 23 A1–A3. Megaclavatula polonica (Pusch, 1837), neotype, NHMW 2021/0138/0001, Korytnica (Poland). B1–B3. Megaclavatula polonica (Pusch, 1837), NHMW 2021/0138/0002, Korytnica (Poland). C1–C3. Megaclavatula polonica (Pusch, 1837), NHMW 2021/0139/0001, Baden-Sooss (Austria).D1–D3. Megaclavatula polonica (Pusch, 1837), NHMW 1862/0001/0324, Bad Vöslau (Austria). E1–E3. Megaclavatula pilleri nov. sp., paratype, NHMW 1949/0005/0051c, Baden-Sooss (Austria). F1–F3. Megaclavatula pilleri nov. sp., paratype, NHMW 1949/0005/0051d, Baden-Sooss (Austria).
FIGURE 31 A1–A3 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 31 A1–A3. Perrona descendens (Hilber, 1879), lectotype, NHMW 1862/0033/0034, Pöls (Austria). B1–B3. Perrona descendens (Hilber, 1879), paralectotype, NHMW 1949/0005/0101, St. Florian (Austria). C1–C3. Perrona descendens (Hilber, 1879), paralectotype, NHMW 1861/0001/0260, Pöls (Austria). D1–D3. Perrona descendens (Hilber, 1879), paralectotype, NHMW 1861/0001/0260a, Pöls (Austria). E1–E3. Perrona floriana (Hilber, 1879), holotype, NHMW 1858/0020/0012, Guglitz at St. Florian (Austria). F1–F2. Perrona ilonae nov. nom., M.61.4367, Szentkút, Mátraverebély (Hungary).
FIGURE 16 A1–A3 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 16 A1–A3. 'Clavatula' veronicae (Hoernes & Auinger, 1891), NHMW 1855/0043/0044d, Lăpugiu de Sus (Romania). B1–B3. 'Clavatula' veronicae (Hoernes & Auinger, 1891), paralectotype, NHMW 1855/0043/0044c, Lăpugiu de Sus (Romania). C1–C2. 'Clavatula' veronicae (Hoernes & Auinger, 1891), paralectotype, NHMW 1855/0043/0044b, Lăpugiu de Sus (Romania). D. 'Clavatula' veronicae (Hoernes & Auinger, 1891), lectotype, NHMW 1855/0043/0044a, Lăpugiu de Sus (Romania). E1–E2. Granulatocincta angelae (Hoernes & Auinger, 1891), lectotype, NHMW 1949/0005/0100a, Lăpugiu de Sus (Romania). F1–F2. Granulatocincta angelae (Hoernes & Auinger, 1891), paralectotype, NHMW ex1949/0005/0100b, Lăpugiu de Sus (Romania). G1–G3. Granulatocincta angelae (Hoernes & Auinger, 1891), paralectotype, NHMW 1949/0005/0099, Möllersdorf (Austria).
FIGURE 14 A1–A3 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 14 A1–A3. 'Clavatula' olgae (Hoernes & Auinger, 1891), paralectotype, NHMW 1862/0001/0552a, Buituri (Romania). B1–B3. 'Clavatula' olgae (Hoernes & Auinger, 1891), lectotype, NHMW 1862/0001/0552, Buituri (Romania). C1–C2. 'Clavatula' vitalisi Strausz, 1955, holotype, M.105, Várpalota (Hungary). D1–D2. 'Clavatula' ariejansseni nov. sp., holotype, NHMW 1847/0058/1220, Seyithasan (Turkey). E1–E2. 'Clavatula' ariejansseni nov. sp., paratype, NHMW 1847/0058/1221, Seyithasan (Turkey).
FIGURE 19 A1–A3 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 19 A1–A3. Granulatocincta schreibersi (Hörnes, 1854), lectotype, NHMW 1846/0037/0315, Steinebrunn (Austria). B1–B3. Granulatocincta schreibersi (Hörnes, 1854), paralectotype, NHMW 2021/0130/0001, Enzesfeld (Austria). C1–C3. Granulatocincta schreibersi (Hörnes, 1854), NHMW 1863/0015/1131, Gainfarn (Austria). D1–D3. Granulatocincta schreibersi (Hörnes, 1854), NHMW 2021/0126/0007, Gainfarn (Austria). E1–E3. Granulatocincta theoderichi nov. sp., holotype, NHMW 2016/0026/0320, Ritzing (Austria). F1–F3. Granulatocincta theoderichi nov. sp., paratype, NHMW 2016/0026/0320b, Ritzing (Austria). G1–G3. Granulatocincta theoderichi nov. sp., paratype, NHMW 1848/0003/0022a, Ritzing (Austria). H1–H3. Granulatocincta theoderichi nov. sp., paratype, NHMW 1848/0003/0022b, Ritzing (Austria).
FIGURE 22 A1–A3 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 22 A1–A3. Megaclavatula laevigata (Eichwald, 1830), NHMW 1846/0037/0308, Baden (Austria). B1–B3. Megaclavatula subsculpta (Schaffer, 1912), lectotype, KM Inv. No. F/1125, Maria Dreieichen (Austria). C1–C2. Megaclavatula nemethi (Kovács & Vicián, 2021), holotype, HNHM, PAL 2021.21.1, Letkés (Hungary). D. Megaclavatula nemethi (Kovács & Vicián, 2021), paratype, NHMW 2021/0002/0003, Letkés (Hungary). E1–E2. Megaclavatula? szontaghyi (Strausz, 1926), holotype, M.116, Bán, Baranya County (Hungary). F. Megaclavatula neudorfensis (Schaffer, 1898), holotype, NHMW 2021/0137/0001, Devínska Nová Ves (Slovakia). G1–G3. Megaclavatula pilleri nov. sp., holotype, NHMW 1949/0005/0051a, Baden-Sooss (Austria). H1–H3. Megaclavatula pilleri nov. sp., paratype, NHMW 1949/0005/0051b, Baden-Sooss (Austria).
FIGURE 32 A1–A3 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 32 A1–A3. Perrona loetschi nov. sp., holotype, NHMW 1949/0005/0102a, Grund (Austria). B1–B2. Perrona loetschi nov. sp., paralectotype, NHMW 1949/0005/0102b, Grund (Austria). C1–C3. Perrona loetschi nov. sp., paralectotype, NHMW 2021/0153/0001, Grund (Austria). D1–D2. Perrona loetschi nov. sp., paralectotype, NHMW 1855/0045/0752, Grund (Austria). E1–E3. Perrona louisae (Hoernes & Auinger, 1891), lectotype, NHMW 1861/0050/0162a, Weinsteig (Austria). F1–F2. Perrona louisae (Hoernes & Auinger, 1891), paralectotype, NHMW1861/0050/0162b, Weinsteig (Austria).
FIGURE 30 A1–A2 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 30 A1–A2. Neoperrona harzhauseri (Kovács & Vicián, 2021), holotype, PAL 2021.24.1, Letkés (Hungary). B1–B3. Neoperrona harzhauseri (Kovács & Vicián, 2021), NHMW 2019/0151/019a, Letkés (Hungary). C1–C. Neoperrona harzhauseri (Kovács & Vicián, 2021), NHMW 2019/0151/019b, Letkés (Hungary). D1–D3. Neoperrona zoltanorum nov. sp., holotype, NHMW 2019/0151/0108a, Letkés (Hungary). E1–E3. Neoperrona zoltanorum nov. sp., NHMW 2019/0151/0108b, Letkés (Hungary).
FIGURE 20 A1–A3 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 20 A1–A3. Megaclavatula amaliae (Hoernes & Auinger, 1891), lectotype, NHMW 1949/0005/0049a, Lăpugiu de Sus (Romania). B1–B3. Megaclavatula amaliae (Hoernes & Auinger, 1891), paralectotype, NHMW 1949/0005/0049b, Lăpugiu de Sus (Romania), C1–C2. Megaclavatula amaliae (Hoernes & Auinger, 1891), NHMW 2021/0132/0001, Baden-Sooss (Austria). D1–D2. Megaclavatula antoniae (Hoernes & Auinger, 1891), Z.PAL.U.W., No BkKG928, Korytnica (Poland). E1–E2. Megaclavatula antoniae (Hoernes & Auinger, 1891), NHMW 1949/0005/0045, Guntersdorf (Austria). F1–F3. Megaclavatula antoniae (Hoernes & Auinger, 1891), holotype, NHMW 1849/0005/0048, Guntersdorf (Austria). G1–G3. Megaclavatula antoniae (Hoernes & Auinger, 1891), NHMW 1949/0005/0045, Guntersdorf (Austria).
FIGURE 37 A1–A3 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 37 A1–A3. Perrona koeberli nov. sp., holotype. NHMW 1949/0005/0105a, Grund (Austria). B1–B3. Perrona koeberli nov. sp., paratype, NHMW 1855/0045/0752a, Grund (Austria). C1–C3. Perrona koeberli nov. sp., paratype, NHMW 1855/0045/0753a, Grund (Austria). D1–D3. Perrona koeberli nov. sp., paratype, NHMW 1949/0005/0105b, Grund (Austria). E1–E3. Perrona oliviae (Hoernes & Auinger 1891), paralectotype, NHMW 1865/0001/0223, Lăpugiu de Sus (Romania). F1–F3. Perrona oliviae (Hoernes & Auinger 1891), lectotype, NHMW 1949/0005/0111a, Lăpugiu de Sus (Romania). G. Perrona oliviae (Hoernes & Auinger 1891), paralectotype, NHMW 1873/0026/0027, Lăpugiu de Sus (Romania).
FIGURE 2 in The Clavatulidae (Gastropoda, Conoidea) of the Miocene Paratethys Sea with considerations on fossil and extant Clavatulidae genera
FIGURE 2. Descriptive terms used in descriptions and measurements to shell morphology, whorl profiles and anal sinus. SL: shell length, MD: maximum diameter, AA: apical angle, LWH: last whorl height, AH: aperture height. AL: aperture length. AW: aperture width.
FIGURE 1 in Extant genus of flat bark beetle (Coleoptera: Silvanidae) with a present-day Australian-southern South American disjunction discovered in Eocene Rovno amber
FIGURE 1. Austronausibius aenigmatista sp. nov., holotype, 6816 [MAIG]: A—habitus, dorsal view; B—habitus, ventral view; C—details of left posterior pronotal and anterior elytral sides, black arrow indicates humeral denticle. Scale bars represent 1.0 mm (A, B) or 0.5 mm (C).
Distribution. It was restricted to NE China. Most extant museum specimens purported to be jubata were collected in the mountain ranges N of Hohot, Nei Mongol S of the Mongolian border. in Bovidae
Distribution. It was restricted to NE China. Most extant museum specimens purported to be jubata were collected in the mountain ranges N of Hohot, Nei Mongol S of the Mongolian border.
Extant species fail to estimate ancestral geographical ranges at older nodes in primate phylogeny
<p>A clade's evolutionary history is shaped, in part, by geographical range expansion, sweepstakes dispersal and local extinction. A rigorous understanding of historical biogeography may therefore yield insights into macroevolutionary dynamics such as adaptive radiation. Modern historical biogeographic analyses typically fit statistical models to molecular phylogenies, but it remains unclear whether extant species provide sufficient signal or if well-sampled phylogenies of extinct and extant taxa are necessary to produce meaningful estimates of past ranges. We investigated the historical biogeography of Primates and their euarchontan relatives using a novel meta-analytical phylogeny of over 900 extant ( n = 419) and extinct ( n = 483) species spanning their entire evolutionary history. Ancestral range estimates for young nodes were largely congruent with those derived from molecular phylogeny. However, node age exerts a significant effect on ancestral range estimate congruence, and the probability of congruent inference dropped below 0.5 for nodes older than the late Eocene, corresponding to the origins of higher-level clades. Discordance was not observed in analyses of extinct taxa alone. Fossils are essential for robust ancestral range inference and biogeographic analyses of extant clades originating in the deep past should be viewed with scepticism without them.</p>
Distribution. Galapagos Is; recorded on Santa Fe, San Cristobal, and Santiago (James) Is, but may only be extant on Santa Fe I. in Cricetidae
Distribution. Galapagos Is; recorded on Santa Fe, San Cristobal, and Santiago (James) Is, but may only be extant on Santa Fe I.
Distribution. Endemic to Japan, widely distributed on Honshu and Kyushu. No recent records of extant distribution but fossil records found on Shikoku. in Soricidae
Distribution. Endemic to Japan, widely distributed on Honshu and Kyushu. No recent records of extant distribution but fossil records found on Shikoku.
FIGURE 179 in The genus Afrocymbella (Bacillariophyceae) from lakes Malawi and Tanganyika, with description of new fossil and extant species
FIGURE 179. Scatterplot of the valve length vs valve width showcasing the differences between A. brunii (circles) and A. gibba sp. nov. (squares) as observed in populations of samples that we collected.
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