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Fig. 7. A. Simocyon batalleri, MSB 24933 in Ailurid carnivoran mammal Simocyon from the late Miocene of Spain and the systematics of the genus

Fig. 7. A. Simocyon batalleri, MSB 24933, Sabadell, Barcelona province, Spain, right maxilla with P4–M2 in occlusal view. B. Simocyon primigenius, MNHN−PIK 3017, Pikermi, Greece, fragmentary left mandible with p4–m1 in lingual (B1), lateral (B2), and dorsal (B3) views.

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Fig. 2. Simocyon batalleri, MNCN B−3458 in Ailurid carnivoran mammal Simocyon from the late Miocene of Spain and the systematics of the genus

Fig. 2. Simocyon batalleri, MNCN B−3458, Batallones−1, Madrid Province, Spain, cranium in dorsal view. A. Photo. B. Schematic drawing showing the main anatomical features of this view (artwork by M. Antón).

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Fig. 4 in Ailurid carnivoran mammal Simocyon from the late Miocene of Spain and the systematics of the genus

Fig. 4. Simocyon batalleri, Batallones−1, Madrid Province, Spain. A. MNCN B−386, right upper canine in, lingual (A1) and buccal (A2) views. B. MNCN B−4337, right lower canine in lingual (B1) and buccal (B2) views.

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Fig. 9 in Ailurid carnivoran mammal Simocyon from the late Miocene of Spain and the systematics of the genus

Fig. 9. Ratio diagram showing the species of Simocyon. The standard is a mean of the entire sample of Simocyon primigenius, including the material assigned to S. zdanskyi and S. marshi.

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Fig. 10. A in Ailurid carnivoran mammal Simocyon from the late Miocene of Spain and the systematics of the genus

Fig. 10. A. Simocyon batalleri, MNCN BAT−1−D7−7−2001, Batallones−1, Madrid Province, Spain, right hemimandible with p1–m1 in lateral view. B. Simocyon primigenius, MNHN−PIK 3020, Pikermi, Greece, right hemimandible with c, p4, m1 and m2 in lateral view.

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Fig. 1 in Ailurid carnivoran mammal Simocyon from the late Miocene of Spain and the systematics of the genus

Fig. 1. Simocyon batalleri (Viret, 1929), MNCN B−3620, Batallones−1, Madrid Province, Spain, cranium in ventral view. A. Photograph. B. Schematic drawing showing the main anatomical features of this view (artwork by M. Antón).

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Fig.. 3. Simocyon batalleri, MNCN B−3458, Batallones−1, Madrid Province, Spain, cranium in left lateral view. A. Photograph. B. Schematic drawing showing the main anatomical features of this view (artwork by M. Antón). in Ailurid carnivoran mammal Simocyon from the late Miocene of Spain and the systematics of the genus

Fig.. 3. Simocyon batalleri, MNCN B−3458, Batallones−1, Madrid Province, Spain, cranium in left lateral view. A. Photograph. B. Schematic drawing showing the main anatomical features of this view (artwork by M. Antón).

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Fig. 7 in Phylogeny, palaeoecology, and invasion of non-marine waters by the late Miocene hemicytherid ostracod Tyrrhenocythere from Lake Pannon

Fig. 7. Length (l) and height (h) ratio of early Tyrrhenocythere species from Pezinok (Danube Basin). The male valves are longer than the female ones.

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Fig. 6 in Phylogeny, palaeoecology, and invasion of non-marine waters by the late Miocene hemicytherid ostracod Tyrrhenocythere from Lake Pannon

Fig. 6. Marginal pore canals on anterior margin and their transformation from straight Hemicytheria arrangement to brush−like Tyrrhenocythere one. A. Hemicytheria reniformis (Reuss, 1850), Hemicytheria folliculosa (Reuss, 1850), Hemicytheria omphalodes (Reuss, 1850), original by author. B. Hemicytheria biornata (Zalányi, 1944), original by author, Hemicytheria maeotica Olteanu 1989 after Olteanu and Vekua (1989). C. Hemicytheria major Sokač, 1972. D. Hemicytheria marginata Sokač, 1972 after Sokać (1972). E. Tyrrhenocythere transitivum sp. nov. F. Tyrrhenocythere pezinokensis (Jiříček, 1985). G. Tyrrhenocythere rastislavi sp. nov. original by author.

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Fig. 2 in Phylogeny, palaeoecology, and invasion of non-marine waters by the late Miocene hemicytherid ostracod Tyrrhenocythere from Lake Pannon

Fig. 2. Geographical sketch (A) and lithological column (B) of Pezinok clay pit (Pipík 1998). C. Detail of the sequence with Tyrrhenocythere mirror swamps and shallow water sedimentation on the bord of freshwater−/miohaline lake (Baráth et al. 1999).

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Fig. 5. Late Miocene hemicytherid ostracods from the layer 36 in Phylogeny, palaeoecology, and invasion of non-marine waters by the late Miocene hemicytherid ostracod Tyrrhenocythere from Lake Pannon

Fig. 5. Late Miocene hemicytherid ostracods from the layer 36+37A in Pezinok, Slovakia. A–C, I, L. Tyrrhenocythere transitivum sp. nov. A. RV♂, paratype, SNM RP27−21, external lateral view. B. LV♂, paratype, SNM RP27−18, external lateral view. C. LV♀, paratype, SNM RP26−4−4, external lateral view. I. LV♀, paratype, SNM RP27−19, internal lateral view; I1, central muscle scars; I2, detail of hinge. L. RV♀, paratype, SNM RP27−22, internal lateral view, detail of hinge. D. Tyrrhenocythere sp. 1, RV, SNM RP27−2, external lateral view; D1, SEM photo; D2, valve in transparent light. F. Tyrrhenocythere sp. 2, RV♀, SNM RP28−2, external lateral view. G, J. Tyrrhenocythere pezinokensis (Jiříček, 1985). G. LV♀, SNM RP27−8, internal lateral view, G1, central muscle scars; G2, detail of hinge. J. RV♀, paratype, SNM RP27−5, internal lateral view, detail of hinge. E, H, K. Tyrrhenocythere rastislavi sp. nov. E. RV♂, paratype, SNM RP26−16−1, external lateral view. H. RV♀, paratype, SNM RP27−15, internal lateral view; H1, central muscle scars; H2, detail of hinge. K. LV♀, paratype, SNM RP27−12, internal lateral view, detail of hinge.

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Fig. 8 in Phylogeny, palaeoecology, and invasion of non-marine waters by the late Miocene hemicytherid ostracod Tyrrhenocythere from Lake Pannon

Fig. 8. Change of salinity tolerance in the course of phylogeny from fully marine/brackish Aurila through brackish Hemicytheria to brackish/freshwater Tyrrhenocythere; black, fully marine; grey, brackish; white, freshwater/oligohaline.

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Fig. 1. A in Phylogeny, palaeoecology, and invasion of non-marine waters by the late Miocene hemicytherid ostracod Tyrrhenocythere from Lake Pannon

Fig. 1. A. Palaeogeographical map of Europe in the upper Miocene (9.5 Ma) (after Steininger and Rögl 1985). B. Lake Pannon in a time of maximum flooding surface in Pannonian zone E (Spiniferites paradoxus Biochron) (after Kováč 2000).

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Figure 2-3 in Nucella demouthae, A New Species of Late Miocene Muricid Gastropod From Northern California, U.S.A.

Figure 2-3. Nucella demouthae Powell, Roth, and Garcia n. sp. CASG holotype 73156. CASG locality 54136. Bloomfield Quarry, north of Bloomfield, Sonoma County, CA. Height 33.5 mm, width 19.2 mm. 2. Adapertural view, 3. Apertural view.

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Figure 14 in Nucella demouthae, A New Species of Late Miocene Muricid Gastropod From Northern California, U.S.A.

Figure 14. Stratigraphic ranges of northeastern Pacific Nucella spp., fossil and modern. See text for references for age range of each species.

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Figure 1 in Nucella demouthae, A New Species of Late Miocene Muricid Gastropod From Northern California, U.S.A.

Figure 1. Index map (A) and stratigraphic column (B) showing the geology of Bloomfield Quarry, Sonoma County, California. California Academy of Sciences, Geology (CASG) fossil localities 54135, 54136, and 57867 are shown. Mrt, informally named Roblar tuff of Sarna-Wojcicki (1992); Ma, megaannum or millions of years ago. After Powell et al. (2019), courtesy of James Allen

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Text-fig. 2. Scatter diagram of the length/width ratio of the upper fourth premolar (P4) of Chalicomys jaegeri from Grytsiv as compared to those of C. jaegeri only (a) and additionally of Euroxenomys minutus rhenanus (E. min rhen), Euroxenomys minutus (Eurex min) (b) from other localities. Abbreviations for localities: Cana – Çanakkale (probably MN 8/9 after Sen 2016; data from Ünay 1974), DornD – Dorn-Dürkheim 1 (MN 11; data from Franzen and Storch (1975) for both C. jaegeri and E. minutus rhenanus), Epp – Eppelsheim (MN 9; Stefen 2009), Kücük – Küçükçekmece (probably MN 8/9; Sen 2016), and Sansan (MN 6 after Sen 1997; data from Hugueney and Duranthon 2012). A single specimen from Grytsiv (G) – NMNHU-P 22/218 is tentatively assigned to Euroxenomys minutus based on its size. in Beavers (Castoridae, Rodentia) From The Late Miocene (Mn 9) Locality Grytsiv In Ukraine

Text-fig. 2. Scatter diagram of the length/width ratio of the upper fourth premolar (P4) of Chalicomys jaegeri from Grytsiv as compared to those of C. jaegeri only (a) and additionally of Euroxenomys minutus rhenanus (E. min rhen), Euroxenomys minutus (Eurex min) (b) from other localities. Abbreviations for localities: Cana – Çanakkale (probably MN 8/9 after Sen 2016; data from Ünay 1974), DornD – Dorn-Dürkheim 1 (MN 11; data from Franzen and Storch (1975) for both C. jaegeri and E. minutus rhenanus), Epp – Eppelsheim (MN 9; Stefen 2009), Kücük – Küçükçekmece (probably MN 8/9; Sen 2016), and Sansan (MN 6 after Sen 1997; data from Hugueney and Duranthon 2012). A single specimen from Grytsiv (G) – NMNHU-P 22/218 is tentatively assigned to Euroxenomys minutus based on its size.

opencc-by-4.0Nov 2020View details →
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Text-fig. 7. Typhlomys hipparionum Q, 1989 from Leilao, Yuanmou. a) left M1 (IVPP V 25885.4), b) right M1 (IVPP V 25885.5), IU c) left M2 (IVPP V 25885.6), d) left M2 (IVPP V 25885.7, reversed), e) left M3 (IVPP V 25885.8), f) right M3 (IVPP V 25885.9), g) left M1 (IVPP V 25885.10), h) right M1 (IVPP V 25885.11), i) left M2 (IVPP V 25885.12), j) right M2 (IVPP V 25885.13), k) left M3 (IVPP V 25885.1), l) left M3 (IVPP V 25885.14, reversed). in Platacanthomyids (Rodentia, Mammalia) From The Late Miocene Yuanmou Hominoid Locality Of Yunnan, China

Text-fig. 7. Typhlomys hipparionum Q, 1989 from Leilao, Yuanmou. a) left M1 (IVPP V 25885.4), b) right M1 (IVPP V 25885.5), IU c) left M2 (IVPP V 25885.6), d) left M2 (IVPP V 25885.7, reversed), e) left M3 (IVPP V 25885.8), f) right M3 (IVPP V 25885.9), g) left M1 (IVPP V 25885.10), h) right M1 (IVPP V 25885.11), i) left M2 (IVPP V 25885.12), j) right M2 (IVPP V 25885.13), k) left M3 (IVPP V 25885.1), l) left M3 (IVPP V 25885.14, reversed).

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Text-fig. 6. Scatter diagrams (length and width) of Typhlomys aff. T. primitivus measurements from Leilao, Yuanmou in comparison with those of T. hipparionum and T. storchi from Leilao, and of T. primitivus and T. hipparionum from Shihuiba, Lufeng. in Platacanthomyids (Rodentia, Mammalia) From The Late Miocene Yuanmou Hominoid Locality Of Yunnan, China

Text-fig. 6. Scatter diagrams (length and width) of Typhlomys aff. T. primitivus measurements from Leilao, Yuanmou in comparison with those of T. hipparionum and T. storchi from Leilao, and of T. primitivus and T. hipparionum from Shihuiba, Lufeng.

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Text-fig. 5. Typhlomys aff. T. primitivus Q, 1989 from Leilao, Yuanmou. a) left M1 (IVPP V 25884.53), b) right M1 (IVPP IU V 25884.54), c) left M2 (IVPP V 25884.55), d) right M2 (IVPP V 25884.14), e) left M3 (IVPP V 25884.56), f) right M3 (IVPP V 25884.57), g) left M1 (IVPP V 25884.15), h) right M1 (IVPP V 25884.58), i) left M2 (IVPP V 25884.59), j) right M2 (IVPP V 25884.60), k) left M3 (IVPP V 25884.61), l) right M2 (IVPP V 25884.62). in Platacanthomyids (Rodentia, Mammalia) From The Late Miocene Yuanmou Hominoid Locality Of Yunnan, China

Text-fig. 5. Typhlomys aff. T. primitivus Q, 1989 from Leilao, Yuanmou. a) left M1 (IVPP V 25884.53), b) right M1 (IVPP IU V 25884.54), c) left M2 (IVPP V 25884.55), d) right M2 (IVPP V 25884.14), e) left M3 (IVPP V 25884.56), f) right M3 (IVPP V 25884.57), g) left M1 (IVPP V 25884.15), h) right M1 (IVPP V 25884.58), i) left M2 (IVPP V 25884.59), j) right M2 (IVPP V 25884.60), k) left M3 (IVPP V 25884.61), l) right M2 (IVPP V 25884.62).

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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