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FIG. 18 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 18. — Thin-section photomicrographs of the fusulinid assemblages of the Yassıpınar (YS), Bademli (BS) and GÖlbelen (GS) sections: A, Fusulinella praebocki Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 16B42.18.02, BS; B, Fusulinella praecolaniae Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 16B38.03, BS; C, D, Fusulinella propriaforma Akba ¸s, n. sp.; C, subaxial section, 16B39.03 (holotype), BS; D, axial section, 16B39.08, BS; E, detailed view of the wall structure of the Fusulinella propriaforma Akba ¸s, n. sp., 16B39.08 (four-layered wall including tectum, diaphanotheca, lower and upper tectorium); F, Fusulinella pseudobocki Lee & Chen in Lee, Chen & Chu, 1930, axial section, 18G56.05, GS; G, H, Fusulinella ex gr. schubertellinoides Putrya, 1938; G, axial section, 16B33.03, BS; H, axial section, 18G41.09, GS; I, J, Fusulinella vozhgalensis devexa Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951; I, axial section, 16B39.07, BS; J, axial section, 18G41.11, GS; K, L, Fusulinella sp. A; K, subaxial section, 16B34.03, BS; L, tangentially section, 16B35.05, BS; M-P, Fusulinella? sp. B; M, axial section, 16B44.03, BS; N, axial section, 16B44.04, BS; O, axial section, 16B45.03, BS; P, axial section, 16B45.08, BS; Q-T, Fusulinella? sp. C; Q, axial section, 16B44.08, BS; R, axial section, 16B44.09, BS; S, axial section, 16B44.13, BS; T, axial section, 16B45.04, BS; U, Protriticites subschwagerinoides subschwagerinoides Rozovskaya, 1950, axial section, 19B48.03, BS; V, W, Protriticites subschwagerinoides inflatus Bensh, 1972; V, axial section, 19B48.10, BS; W, axial section, 19B50.04, BS; X, Montiparus ex gr. priscus (Villa in Villa & Martinez-Garcia, 1989), axial section, 18G59.03, GS. Scale bar: 1 mm except E, 500 µm.
FIG. 17 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 17. — Thin-section photomicrographs of the fusulinid assemblages of the Yassıpınar (YS), Bademli (BS) and GÖlbelen (GS) sections: A-E, Fusulinella absoluta Akba ¸s, n. sp.; A, axial section, 16B38.04, BS; B, subaxial section, 16B38.09, BS; C, subaxial section, 16B38.10 (Holotype), BS; D, axial section, 16B38.11, BS; E, axial section, 16B40.07, BS; F, detailed view of the wall structure of the Fusulinella absoluta Akba ¸s, n. sp., 16B38.10 (holotype) (four-layered wall including tectum, diaphanotheca, lower and upper tectorium); G, H, Fusulinella bocki bocki MÖller, 1878; G, axial section, 16B42.03, BS; H, axial section, 18G48.06, GS; I, Fusulinella bocki pauciseptata Rauzer-Chernousova & Belyaev in Rauzer-Chernousova, Belyaev & Reitlinger, 1936, axial section, 16B43.22, BS; J, Fusulinella cf. bocki timanica Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 15Y39.05, YS; K, Fusulinella cf. colaniae colaniae Lee & Chen in Lee, Chen & Chu, 1930, axial section, 18G56.04, GS; L, Fusulinella colaniae meridionalis Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 15Y39.11, YS; M, Fusulinella cf. eopulchra Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 15Y37.03, YS; N, O, Fusulinella helenae Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951; N, axial section, 18G57.06, GS; O, axial section, 18G58.03, GS; P-R, Fusulinella obtusa minuta Akba ¸s, n. subsp.; P, axial section, 15Y37.07, YS; Q, axial section, 15Y37.08.01 (Holotype), YS; R, axial section, 15Y38.04, YS; S, detailed view of the wall structure of the Fusulinella obtusa minuta Akba ¸s, n. subsp., 15Y37.08.01 (holotype) (four-layered wall including tectum, diaphanotheca, lower and upper tectorium); T-V, Fusulinella paracolaniae Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951; T, axial section, 16B43.07, BS; U, axial section, 18G51.06, GS; V, axial section, 18G51.09, GS. Scale bar: 1 mm except F, S, 500 µm.
FIG. 15 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 15. — Thin-section photomicrographs of the fusulinid assemblages of the Yassıpınar (YS), Bademli (BS) and GÖlbelen (GS) sections:A, Praefusulinella guvenci Akba ¸s, n. gen., n. sp., axial section, 18G40.20, GS; B, detailed view of the wall structure of the Praefusulinella guvenci Akba ¸s, n. gen., n. sp., 18G40.16 (four-layered wall including tectum, diaphanotheca, lower and upper tectorium); C-G, Praefusulinella okuyucui Akba ¸s, n. gen., n. sp.; C, subaxial section, 16B38.13, BS; D, axial section, 18G40.03, GS; E, axial section, 18G40.07 (Holotype), GS; F, axial section, 18G40.18, GS; G, axial section, 18G41.10, GS; H, detailed view of the wall structure of the Praefusulinella okuyucui Akba ¸s, n. gen., n. sp., 18G40.03 (four-layered wall including tectum, diaphanotheca, lower and upper tectorium). Scale bar: 1 mm except B, H, 500 µm.
FIG. 16 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 16. — Thin-section photomicrographs of the fusulinid assemblages of the Yassıpınar (YS), Bademli (BS) and GÖlbelen (GS) sections: A-C, Praefusulinella rhombiforma Akba ¸s, n. gen., n. sp.; A, axial section, 18G40.06, GS; B, axial section, 18G40.10, GS; C, axial section, 18G40.11 (Holotype), GS; D, detailed view of the wall structure of the Praefusulinella rhombiforma Akba ¸s, n. gen., n. sp., 18G40.11 (holotype) (four-layered wall including tectum, diaphanotheca, lower and upper tectorium); E-I, Praefusulinella tekini Akba ¸s, n. gen., n. sp.; E, axial section, 18G40.12, GS; F, axial section, 18G40.13, GS; G, axial section, 18G40.15, GS; H, axial section, 18G40.17.01, GS; I, axial section, 18G40.21 (holotype), GS; J, detailed view of the wall structure of the Praefusulinella tekini Akba ¸s, n. gen., n. sp., 18G40.21 (holotype) (four-layered wall including tectum, diaphanotheca, lower and upper tectorium). Scale bar: 1 mm except D, J, 500 µm.
FIG. 14 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 14. — Thin-section photomicrographs of the fusulinid assemblages of the Yassıpınar (YS), Bademli (BS) and GÖlbelen (GS) sections: A-D, Beedeina schellwieni (Staff in Schellwien & Staff, 1912); A, axial section, 16B40A.09, BS; B, axial section, 16B40C.11, BS; C, axial section, 18G41.15, GS; D, oblique section, 18G45.07, GS; E, F, Beedeina tauridiana Akba ¸s, n. sp.; E, axial section, 16B41.07 (Holotype), BS; F, axial section, 16B41.08, BS; G, detailed view of the wall structure of the Beedeina tauridiana Akba ¸s, n. sp., 16B41.08 (Four layered wall including tectum, diaphanotheca, lower and upper tectorium); H, I, Beedeina timanica (Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951); H, subaxial section, 16B40C.06, BS; I, axial section, 16B40C.18, BS; J, K, Eofusulina binominata Putrya, 1956; J, axial section, 15Y34.04, YS; K, subaxial section, 18G31.06, GS; L, M, Eofusulina triangula (Rauzer-Chernousova & Belyaev in Rauzer-Chernousova, Belyaev & Reitlinger, 1936); L, axial section, 15Y25.06, YS; M, axial section, 15Y27.04, YS; N, O, Praefusulinella guvenci Akba ¸s, n. gen., n. sp.; N, axial section, 18G40.14 (holotype), GS; O, axial section, 18G40.16, GS. Scale bar: 1 mm except G, 500 µm.
FIG. 13 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 13. — Thin-section photomicrographs of the fusulinid assemblages of the Yassıpınar (YS), Bademli (BS) and GÖlbelen (GS) sections: A, Quasifusulinoides cf. juvenatus Kireeva in Bogush, 1963, subaxial section, 19B48.08, BS; B, Quasifusulinoides quasifusulinoides (Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951), axial section, 19B48.06, BS; C, D, Beedeina elegans (Rauzer-Chernousova & Belyaev in Rauzer-Chernousova, Belyaev & Reytlinger, 1940); C, subaxial section, 16B40B.08, BS; D, subaxial section, 18G48.03, GS; E, F, Beedeina minuta Akba ¸s, n. sp.; E, axial section, 18G41.03 (Holotype), GS; F, axial section, 18G41.06, GS; G, detailed view of the wall structure of the Beedeina minuta Akba ¸s, n. sp., 18G41.06 (Four layered wall including tectum, diaphanotheca, lower and upper tectorium); H, Beedeina cf. nytvica callosa (Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951), axial section, 18G55.03, GS; I, Beedeina paradistenta (Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951), axial section, 16B41.16, BS; J-M, Beedeina pseudoelegans pseudoelegans (Chernova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951); J, axial section, 15Y36.04, YS; K, axial section, 15Y36.09, YS; L, subaxial section, 16B40C19.01, BS; M, subaxial section, 18G45.06.02, GS; N, Beedeina pseudoelegans keltmensis (Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951), axial section, 16B41.11, BS; O, P, Beedeina samarica (Rauzer-Chernousova & Belyaev in Rauzer-Chernousova, Belyaev & Reytlinger, 1940); O, axial section, 16B40B.05, BS; P, axial section, 18G45.03, GS. Scale bar: 1 mm except A, B, 2 mm; G, 500 µm.
FIG. 10 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 10. — Thin-section photomicrographs of the fusulinid assemblages of the Yassıpınar (YS), Bademli (BS) and GÖlbelen (GS) sections: A, B, Depratina chernovi (Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951); A, axial section, 15Y22.06, YS; B, axial section, 15Y23.06, YS; C, Depratina convoluta (Lee & Chen in Lee, Chen & Chu, 1930), axial section, 15Y23.07.01, YS; D, E, Depratina dubia (Villa, 1995); D, axial section, 15Y28.12, YS; E, axial section, 15Y29.08.01, YS; F, G, Depratina paratimanica (Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951); F, axial section, 15Y24.10, YS; G, axial section, 18G29.03, GS; H, I, Depratina posadai (Villa, 1995); H, axial section, 15Y24.04, YS; I, axial section, 18G29.13, GS; J-M, Depratina prisca prisca (Deprat, 1912); J, axial section, 15Y23.08, YS; K, axial section, 15Y28.09.02, YS; L, axial section, 18G27.04, GS; M, axial section, 18G28.08.02, GS; N, O, Depratina prisca sphaeroidea (Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951); N, axial section, 15Y31.06, YS; O, subaxial section, 18G32.06.01, GS; P-S, Depratina prisca timanica (Kireeva in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951); P, axial section, 15Y21.13, YS; Q, axial section, 15Y24.11, YS; R, axial section, 18G27.19, GS; S, axial section, 18G28.14.01, GS; T, U, Depratina sitteri (van Ginkel, 1987); T, axial section, 15Y21.03, YS; U, axial section, 18G29.17, GS; V, W, Staffellaeformes tashliensis (Lebedeva in Grozdilova, Lebedeva, Lipina, Malakhova, Mikhailova, Chermnykh, Postoyalko, Simonova, Sinitsyna, Krylova, Grozdilova, Pozner & Sultanaev, 1975); V, axial section, 15Y23.03, YS; W, axial section, 18G23.12, GS; X-Z, Taitzehoella librovitchi (Dutkevich, 1934); X, axial section, 15Y36.17, YS; Y, subaxial section, 16B36.03, BS; Z, subaxial section, 16B40.05, BS. Scale bar: 500 µm.
FIG. 11 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 11. — Thin-section photomicrographs of the fusulinid assemblages of the Yassıpınar (YS), Bademli (BS) and GÖlbelen (GS) sections:A, B, Taitzehoella mutabilis (Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951); A, axial section, 15Y35.04, YS; B, axial section, 18G32.08, GS; C, D, Taitzehoella praelibrovichi (Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951); C, subaxial section, 15Y35.03, YS; D, subaxial section, 18G39.03, GS; E-G, Aljutovella aljutovica (Rauzer-Chernousova, 1938); E, subaxial section, 15Y21.16.01, YS; F, axial section, 15Y21.42, YS; G, axial section, 18G27.03, GS; H, I, Aljutovella arrisionis arrisionis Leontovich in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Cherno- va, 1951; H, axial section, 18G27.20, GS; I, axial section, 18G28.07.02, GS; J, Aljutovella arrisionis molotovensis Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 15Y21.21, YS; K, L, Aljutovella artificialis Leontovich in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951; K, axial section, 16B33.06, BS; L, subaxial section, 18G28.06, GS; M, Aljutovella cf. cafirniganica Bensh 1969, axial section, 18G28.10, GS; N, Aljutovella conspecta Leontovich in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 18G28.23, GS; O, P, Aljutovella cybaea Leontovich in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951; O, axial section, 15Y27.06, YS; P, axial section, 15Y30.07, YS; Q, Aljutovella isvarica Putrya 1956, axial section, 18G31.03, GS; R, Aljutovella lepida novoburasiensis Leontovich in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 18G29.15, GS. Scale bar: 1 mm.
FIG. 9 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 9. — Thin-section photomicrographs of the fusulinid assemblages of the Yassıpınar (YS), Bademli (BS) and GÖlbelen (GS) sections: A, Schubertella obscura obscura Lee & Chen in Lee, Chen & Chu, 1930, axial section, 15Y22.03.02, YS; B, Profusulinella parafittsi Rauzer-Chernousova & Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 18G33.09, GS; C, D, Profusulinella pararhomboides Rauzer-Chernousova & Belyaev in Rauzer-Chernousova, Belyaev & Reitlinger, 1936; C, axial section, 15Y30.09, YS; D, subaxial section, 18G27.12, GS; E, F, Profusulinella pseudorhomboides Putrya & Leontovich, 1948; E, oblique section, 15Y22.07, YS; F, axial section, 15Y25.14, YS; G, Profusulinella rhombiformis nibelensis (Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951), axial section, 15Y25.04, YS; H, I, Profusulinella rhomboides (Lee & Chen in Lee, Chen & Chu, 1930); H, axial section, 15Y19.06, YS; I, subaxial section, 18G31.07, GS; J, Solovievaia arta (Leontovich in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951), axial section, 15Y28.07.02, YS; K, Solovievaia ex gr. nuratavensis (Solovieva, 1977), axial section, 18G26.07, GS; L, M, Solovievaia ovata ovata (Rauzer-Chernousova, 1938); L, axial section, 15Y21.33.02, YS; M, axial section, 18G28.21, GS; N, O, Solovievaia ovata nytvica (Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951); N, axial section, 15Y21.28, YS; O, axial section, 18G32.16, GS; P, Solovievaia simplex (Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951), n. comb., axial section, 18G33.14, GS; Q, Solovievaia subovata (Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951), axial section, 15Y24.20, YS; R, S, Solovievaia syzranica (Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951), n. comb.; R, axial section, 18G33.12, GS; S, axial section, 18G33.15, GS. Scale bar: 1 mm except A, 250 µm.
FIG. 2 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 2. — Generalized columnar section of the Hadim Nappe (modified after Güvenç 1977a, b; Monod 1977; Turan 1990; Okuyucu & Güvenç 1997; Özgül 1997). Abbreviation: U.C., Upper Cretaceous.
FIG. 6 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 6. — Total stratigraphic distribution of fusulinids from the Moscovian to lower Kasimovian in this study.
FIG. 8 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 8. — Thin-section photomicrographs of the fusulinid assemblages of the Yassıpınar (YS), Bademli (BS) and GÖlbelen (GS) sections: A, Neostaffella nibelensis (Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951), axial section, 15Y31.05, YS; B, Neostaffella ozawai ozawai (Lee & Chen in Lee, Chen & Chu, 1930), axial section, 18G49.03, GS; C, D, Neostaffella ozawai compacta (Manukalova, 1950); C, axial section, 15Y34.03, YS; D, subaxial section, 18G49.04, GS; E, F, Neostaffella sphaeroidea sphaeroidea (Ehrenberg, 1842); E, axial section, 15Y29.12, YS; F, axial section, 18G32.22, GS; G, H, Neostaffella sphaeroidea cuboides (Rauzer-Chernousova in Rauzer-Chernousova,Gryzlova, Kireeva,Leontovich, Safonova & Chernova, 1951); G, axial section, 15Y36.07.01,YS; H, subaxial section, 18G32.09, GS; I, J, Neostaffella subquadrata (Grozdilova & Lebedeva, 1950); I, subaxial section, 15Y31.08, YS;J, axial section, 18G32.10, GS; K, L, Neostaffella umbilicata (Putrya & Leontovich, 1948); K, axial section, 15Y36.06, YS; L, subaxial section, 15Y36.15.01, YS. Scale bar: 500 µm.
FIG. 7 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 7. — Thin-section photomicrographs of the fusulinid assemblages of the Yassıpınar (YS), Bademli (BS) and GÖlbelen (GS) sections: A, Eostaffella kashirica Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 18G27.18, GS; B, Ozawainella angulata (Colani, 1924), subaxial section, 15Y36.18, YS; C, D, Ozawainella crassiformis Putrya, 1956; C, axial section, 15Y36.20, YS; D, axial section, 16B43.15, BS; E, Ozawainella krasnokamski Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 15Y39.12, YS; F, Ozawainella kumpani Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 18G41.12, GS; G, H, Ozawainella kurachovensis Manukalova, 1950; G, subaxial section, 16B42.09, BS; H, subaxial section, 18G41.05, GS; J, K, Ozawainella leei (Putrya, 1939); J, subaxial section, 15Y29.09, YS; K, subaxial section, 16B42.26, BS; L, M, Ozawainella mosquensis Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951; L, subaxial section, 16B43.11, BS; M, axial section, 18G41.16, GS; N, Ozawainella paratingi Manukalova, 1950, axial section, 15Y39.15, YS; O, Ozawainella pseudorhomboidalis Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951, axial section, 16B42.08, BS; P, Ozawainella tingi (Lee, 1937), subaxial section, 18G40.08, GS; Q-R, Ozawainella quadrata Kireeva, 1949; Q, axial section, 15Y37.05, YS; R, axial section, 18G42.04, GS; S, Neostaffella cf. formosa (Rauzer-Chernousova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951), axial section, 18G34.03, GS; T, Neostaffella larionovae polasnensis (Rauzer-Chernousova & Safonova in Rauzer-Chernousova, Gryzlova, Kireeva, Leontovich, Safonova & Chernova, 1951) subaxial section, 18G34.07.02, GS. Scale bar: 500 µm except A, 250 µm.
Text-fig. 4. Lepidocarpon cone in the process of disaggregating as part of the dispersal strategy of the plants. When preserved isolated, the sporophylls are assigned to the fossil-genus Lepidostrobophyllum. Refigured from Thomas (1981). Grovesend Formation (upper Asrturian – lower Moscovian), Kilmersdon Tip, Radstock Coalfield, UK; Natural History Museum (London) specimen V.60431. in Naming Of Parts: The Use Of Fossil-Taxa In Palaeobotany
Text-fig. 4. Lepidocarpon cone in the process of disaggregating as part of the dispersal strategy of the plants. When preserved isolated, the sporophylls are assigned to the fossil-genus Lepidostrobophyllum. Refigured from Thomas (1981). Grovesend Formation (upper Asrturian – lower Moscovian), Kilmersdon Tip, Radstock Coalfield, UK; Natural History Museum (London) specimen V.60431.
Data from: Evolution of the conodont Diplognathodus ellesmerensis from D. benderi sp. nov. at the Bashkirian-Moscovian (Lower-Middle Pennsylvanian) boundary in South China
Conodont assemblages from the Bashkirian-Moscovian boundary interval in the Naqing section, South China have been studied in detail. A landmark-based geometric morphometric analysis to study the evolution of Diplognathodus ellesmerensis is presented. This analysis helped recognize a distinct new species, D. benderi sp. nov., which represents the direct evolutionary ancestor of D. ellesmerensis. The potential of using the First Appearance Datum (FAD) of D. ellesmerensis as the Bashkirian-Moscovian boundary marker is re-evaluated via biostratigraphic correlations of conodonts and other fossil groups between different palaeogeographic basins. The FAD of D. ellesmerensis from within the D. benderi sp. nov.–D. ellesmerensis lineage is an excellent marker to recognize a global Bashkirian-Moscovian boundary because of its global distribution, an abundance of supplementary marker species at similar stratigraphic levels, and the close stratigraphic proximity of the FAD to the traditional Bashkirian-Moscovian boundary, thus largely preserving the original concept for the base of the Moscovian Stage.
FIG. 5 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 5. — Lithostratigraphy and fusulinid distribution of the Bademli section.
FIG. 4 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 4. — Lithostratigraphy and fusulinid distribution of the GÖlbelen section.
FIG. 3 in Fusulinid Biostratigraphy of the Moscovian- Lower Kasimovian of Hadim Nappe, Central Taurides, southern Turkey
FIG. 3. — Lithostratigraphy and fusulinid distribution of the Yassıpınar section.
Data from: Evolution of the conodont Diplognathodus ellesmerensis from D. benderi sp. nov. at the Bashkirian-Moscovian (Lower-Middle Pennsylvanian) boundary in South China
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Data from: Fish and tetrapod communities across a marine to brackish salinity gradient in the Pennsylvanian (early Moscovian) Minto Formation of New Brunswick, Canada, and their palaeoecological and palaeogeographical implications
Euryhaline adaptations in Pennsylvanian vertebrates allowed them to inhabit the marine to freshwater spectrum. This is illustrated by new assemblages of fish and tetrapods from the early Moscovian Minto Formation of New Brunswick, Canada. Fish include chondrichthyans (xenacanthids and the enigmatic Ageleodus), acanthodians (gyracanthids and acanthodiforms), sarcopterygians (rhizodontids, megalichthyids and dipnoans), and actinopterygians (eurynotiforms). Tetrapods include small- to medium-sized, and largely aquatic, stem tetrapods (colosteids) and anthracosaurs (embolomeres). A key finding is that the parautochthonous fossil assemblages are preserved across a salinity gradient, with diversity (measured by the Simpson Index) declining from open marine environments, through brackish embayments, and reaching a nadir in tidal estuaries. Chondrichthyans dominate the entire salinity spectrum (65% of fossils), a distribution that demonstrates a euryhaline mode of life, and one large predatory chondrichthyan, Orthacanthus, may have practised filial cannibalism in coastal nurseries because its heteropolar coprolites contain juvenile xenacanthid teeth. In contrast, other fish communities were more common in open marine settings while tetrapods were more common in coastal brackish waters. While all these faunas were also likely to have been euryhaline, their osmoregulation was, perhaps, less versatile. The demonstration of widespread euryhalinity among fish and aquatic tetrapods explains why Pennsylvanian faunas generally show a cosmopolitan biogeography because taxa were able to disperse via seaways. It also resolves the paradox of enriched strontium isotopic signatures observed in these faunas because organisms would have been, at times, exposed to continental water bodies as well. Therefore, our new findings contribute to the long-running debate about the ecology of Pennsylvanian fishes and tetrapods.
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