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Fig. 1. A in New Stratigraphic Data from the Erlian Basin: Implications for the Division, Correlation, and Definition of Paleogene Lithological Units in Nei Mongol (Inner Mongolia)
Fig. 1. A. Localities (black dots) of the Erlian Basin, Nei Mongol (Inner Mongolia). The shaded area indicates the location of the Nuhetingboerhe-Huheboerhe area (NHA). B. Topographic map of NHA. The black bars indicate positions of measured sections at the Daoteyin Obo, Nuhetingboerhe, Wulanboerhe (Huheboerhe of Meng et al., 2004), and Huheboerhe.
Text-fig. 6. Selected carpological remains from Remigiusberg Formation. A) cf. Samaropsis sp., Inv.-Nr. PB 2016/5038 LS (LS-RLP); B) cf. Samaropsis sp., Inv.-Nr. PB 2016/5029a LS (LS-RLP). in New Data On The Macroflora Of The Basal Rotliegend Group (Remigiusberg Formation; Gzhelian) In The Saar-Nahe Basin (Sw-Germany)
Text-fig. 6. Selected carpological remains from Remigiusberg Formation. A) cf. Samaropsis sp., Inv.-Nr. PB 2016/5038 LS (LS-RLP); B) cf. Samaropsis sp., Inv.-Nr. PB 2016/5029a LS (LS-RLP).
Text-fig. 1. Geological overview map of Saar-Nahe Basin (modified from Stapf (1990) and Uhl et al. (2004)). Asterisk (✽) marks position of localities at Remigiusberg. in New Data On The Macroflora Of The Basal Rotliegend Group (Remigiusberg Formation; Gzhelian) In The Saar-Nahe Basin (Sw-Germany)
Text-fig. 1. Geological overview map of Saar-Nahe Basin (modified from Stapf (1990) and Uhl et al. (2004)). Asterisk (✽) marks position of localities at Remigiusberg.
Text-fig. 5. Pteridosperm remains from Remigiusberg Formation. A) Autunia conferta, coll. Emrich, scalebar = 2 cm; B) "Sphenopteris" germanica, Inv.-Nr. PB 2010/5806 LS (LS-RLP), scalebar = 2.5 cm; C) "Sphenopteris" germanica, Inv.-Nr. PB 2016/5029b LS (LS-RLP), scalebar = 2 cm. in New Data On The Macroflora Of The Basal Rotliegend Group (Remigiusberg Formation; Gzhelian) In The Saar-Nahe Basin (Sw-Germany)
Text-fig. 5. Pteridosperm remains from Remigiusberg Formation. A) Autunia conferta, coll. Emrich, scalebar = 2 cm; B) "Sphenopteris" germanica, Inv.-Nr. PB 2010/5806 LS (LS-RLP), scalebar = 2.5 cm; C) "Sphenopteris" germanica, Inv.-Nr. PB 2016/5029b LS (LS-RLP), scalebar = 2 cm.
Text-fig. 4. Bivariate plots of the upper teeth (M2 – P3) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1914, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2007), Holroyd (1999), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017). in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 4. Bivariate plots of the upper teeth (M2 – P3) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1914, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2007), Holroyd (1999), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017).
Text-fig. 3. Bivariate plots of the lower teeth (m3 – m2) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2003, 2007, 2008, 2010), Holroyd (1999), Morlo et al. (2007), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017). in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 3. Bivariate plots of the lower teeth (m3 – m2) of small to medium sized Miocene hyaenodonts from African localities. Data source: Pilgrim (1912, 1932), Colbert (1935), Savage (1965), Barry (1988), Morales et al. (1998a, 2003, 2007, 2008, 2010), Holroyd (1999), Morlo et al. (2007), Rasmussen et al. (2009), Borths et al. (2016), Borths and Seiffert (2017).
Text-fig. 7. Bivariate plots of the upper teeth (M2, M1, P4) and lower teeth (m3, m2, p4) of large Miocene hyaenodonts from Eurasian and African localities. Data source: Stromer (1926), Savage (1965), Barry (1988), Ginsburg (1999), Holroyd (1999), Morales et al. (2003, 2007, 2008, 2010), Morlo et al. (2007), Rasmussen and Gutiérrez (2009), Borths et al. (2016). in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 7. Bivariate plots of the upper teeth (M2, M1, P4) and lower teeth (m3, m2, p4) of large Miocene hyaenodonts from Eurasian and African localities. Data source: Stromer (1926), Savage (1965), Barry (1988), Ginsburg (1999), Holroyd (1999), Morales et al. (2003, 2007, 2008, 2010), Morlo et al. (2007), Rasmussen and Gutiérrez (2009), Borths et al. (2016).
Text-fig. 10. Phylogenetic relationships of Miocene hyaenodonts (for definitions of character states see Table 2). The data matrix was compiled in MacClade 4.05 and run in PAUP 4.0b10 (Macintosh version). We chose Cimolestes magnus CLEMENS et RUSSELL, 1965, (additional data from Lillegraven 1969), as the outgroup. The unordered and unweighted analysis produced 16 trees. a: Majority-rule consensus. b: Strict consensus. Consistency index (CI): 0.5882; Homoplasy index (HI): 0.4118; Retention index (RI): 0.7742. in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)
Text-fig. 10. Phylogenetic relationships of Miocene hyaenodonts (for definitions of character states see Table 2). The data matrix was compiled in MacClade 4.05 and run in PAUP 4.0b10 (Macintosh version). We chose Cimolestes magnus CLEMENS et RUSSELL, 1965, (additional data from Lillegraven 1969), as the outgroup. The unordered and unweighted analysis produced 16 trees. a: Majority-rule consensus. b: Strict consensus. Consistency index (CI): 0.5882; Homoplasy index (HI): 0.4118; Retention index (RI): 0.7742.
Fig. 5 in New Data on Miocene Butterflies in Dominican Amber (Lepidoptera: Riodinidae and Nymphalidae) with the Description of a New Nymphalid
Fig. 5. Male genitalic valves of fossil and Recent species of Dynamine. All specimens are from the AMNH collection. All to same scale.
Fig. 2 in New Data on Miocene Butterflies in Dominican Amber (Lepidoptera: Riodinidae and Nymphalidae) with the Description of a New Nymphalid
Fig. 2. Photomicrographs of Miocene butterflies in Dominican amber. a. Female of Voltinia dramba (AMNH DR-18-1) in ventral view, and complete view of the amber piece. b. Apical tibial spur in the hind leg of the same specimen. c. Dorsal view of the new Voltinia dramba specimen; this butterfly is fossilized with the wings at an angle and so this image was made with six consecutive pictures of the specimen taken at successive focal planes. d. Male of Dynamine alexae n.sp. holotype (AMNH DR-18-2) in dorsal (left) and ventral view (right). Scale bars 5 1 cm in panels a, c, d; 5 0.1 mm in panel b.
Fig. 1 in New Data on Miocene Butterflies in Dominican Amber (Lepidoptera: Riodinidae and Nymphalidae) with the Description of a New Nymphalid
Fig. 1. Camera lucida drawings of the new specimen of Voltinia dramba (AMNH DR-18-1) in Miocene amber from the Dominican Republic. a. Complete dorsal view of body with the color forewing pattern. b. Hind wing with the color pattern preserved. c. Ventral view of body. d. Hind leg. e. Female genitalia. a–c to same scale.
Fig. 3 in New Data on Miocene Butterflies in Dominican Amber (Lepidoptera: Riodinidae and Nymphalidae) with the Description of a New Nymphalid
Fig. 3. Camera lucida drawings of Dynamine alexae n.sp. (AMNH DR-18-2) in Miocene amber from the Dominican Republic, holotype. a. Body ventral view with the hind-wing color pattern preserved. b. View of the upper side of the forewing, showing the preserved color pattern. c. Male genitalia. d. Hind leg. a–b to same scale.
Fig. 4 in New Data on Miocene Butterflies in Dominican Amber (Lepidoptera: Riodinidae and Nymphalidae) with the Description of a New Nymphalid
Fig. 4. Fossil and Recent wing venations and underside color patterns in males of the genus Dynamine. The reconstruction of the underside color pattern of Dynamine alexae n.sp. is adapted from several Recent species of Dynamine (fig. 3 shows the partly preserved color pattern), and the reconstruction of the wing venation (depicted as gray lines) is adapted from the venation of D. egaea zetes from Hispaniola. All specimens are from the AMNH collection. All to same scale.
Fig. 6 in Three new species of Ligophorus Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae) from Moolgarda buchanani (Bleeker) off Johor, Malaysia based on morphological, morphometric and molecular data
Fig. 6. Sclerotised hard parts of L. grandis, new species: A, dorsal anchors; B, dorsal bar; C, ventral anchors; D, ventral bar (dorsal view); E, marginal hook; F, male copulatory organ.
Fig. 5 in Three new species of Ligophorus Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae) from Moolgarda buchanani (Bleeker) off Johor, Malaysia based on morphological, morphometric and molecular data
Fig. 5. Sclerotised hard parts of L. liewi, new species (A–F) and L. johorensis, new species (G–L): A & G, dorsal anchors; B & H, dorsal bar; C & I, ventral anchors; D & J, ventral bar (dorsal view); E & K, marginal hook; F & L, male copulatory organ.
Fig. 3 in Three new species of Ligophorus Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae) from Moolgarda buchanani (Bleeker) off Johor, Malaysia based on morphological, morphometric and molecular data
Fig. 3. Maximum-parsimony (MP) trees generated from (A) 28S dataset and (B) 28S+ITS1 dataset using PAUP* with Ergenstrema mugilis as the outgroup. Percentages of the bootstrap values are shown along the branches. *denotes new species
Fig. 1 in Three new species of Ligophorus Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae) from Moolgarda buchanani (Bleeker) off Johor, Malaysia based on morphological, morphometric and molecular data
Fig. 1. Principal Component Analysis (PCA) scatterplot of 465 Ligophorus specimens based on all hard parts (marginal hook, anchors, bars and male copulatory organ). Vertical and horizontal bar plots indicate one-dimensional summary of the principal component axes, PC1 and PC2.
Fig. 2 in Three new species of Ligophorus Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae) from Moolgarda buchanani (Bleeker) off Johor, Malaysia based on morphological, morphometric and molecular data
Fig. 2. Dendrogram of 62 Ligophorus species based on characteristics of all hard parts (anchors, bars and copulatory organ). The arrows on the far right indicate the positions of the three new species: L. liewi, L. johorensis and L. grandis.
Fig. 4 in Three new species of Ligophorus Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae) from Moolgarda buchanani (Bleeker) off Johor, Malaysia based on morphological, morphometric and molecular data
Fig. 4. Photomicrographs of the sclerotised hard parts Ligophorus liewi, new species (A & B), L. johorensis, new species (C & D) and L. grandis, new species (E & F). A, C & E, anchors and bars; B, D & F, male copulatory organ.
Text-fig. 3. Scatter diagrams of a) upper and b) lower teeth from BRS 25 (black profile), French localities (cyan; data from Crochet 1986) and Moncucco Torinese (red ones; unpublished data). in New Light On Parasorex Depereti (Erinaceomorpha: Erinaceidae: Galericini) From The Late Messinian (Mn 13) Of The Monticino Quarry (Brisighella, Faenza, Italy)
Text-fig. 3. Scatter diagrams of a) upper and b) lower teeth from BRS 25 (black profile), French localities (cyan; data from Crochet 1986) and Moncucco Torinese (red ones; unpublished data).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.