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FIG. 6 in Re-assessment of the suids from the Sables marins de Montpellier and selection of a lectotype for Sus provincialis Blainville, 1847

FIG. 6. — Bivariate plots of upper and lower cheek teeth of suids from the Sables marins de Montpellier, France. Abbreviations: a, Dasychoerus arvernensis (Croizet & Jobert, 1828); k, Dasychoerus sp. from Kvabebi; s, Dasychoerus strozzii (Meneghini, 1862); ○, "Sus" provincialis Blainville, 1847, lower teeth; ●, "Sus" provincialis, upper teeth; à, lectotype right M3/ of "Sus" provincialis.

FIG. 3 in Re-assessment of the suids from the Sables marins de Montpellier and selection of a lectotype for Sus provincialis Blainville, 1847

FIG. 3. — Casts of some of the specimens attributed to Sus provincialis Blainville, 1847 by Gervais (1850) housed at the MNHN: A, corresponds to his plate 22, fig. 8 in buccal (A1), stereo occlusal (A2) and lingual (A3) views; B, corresponds to his plate 3, fig. 3 in lingual (B1), occlusal (B2) and buccal (B3) views; C, corresponds to his plate 3, fig. 6 in lingual (C1), stereo occlusal (C2) and buccal (C3) views. B is here attributed to Dasychoerus strozzii (Meneghini, 1862). Scale bar: 10 mm.

FIG. 1 in Re-assessment of the suids from the Sables marins de Montpellier and selection of a lectotype for Sus provincialis Blainville, 1847

FIG. 1. — Blainville's (1847) hypodigm of Sus provincialis Blainville, 1847 from Montpellier: A, corresponds to UM SM 460, right M3/ which is here designated as the lectotype of the species; B, corresponds to UM SM 394, left D4/ (illustrated in reverse); C,corresponds to a specimen (right m/2-m/3 illustrated in reverse) housed in the MNHN which may be the specimen attributed to Sus strozzii Meneghini, 1862 by Fejfar (1964).

FIG. 5 in Re-assessment of the suids from the Sables marins de Montpellier and selection of a lectotype for Sus provincialis Blainville, 1847

FIG. 5. — Dasychoerus strozzii (Meneghini, 1862) from the Sables marins de Montpellier (MNHN.F.MON13), views of the distal end of the m/3 to show grooves and undulations in the walls of the talonid: A, oblique slightly lingual view; B, distal view showing buccally tilted distal root; C, oblique slightly buccal view. Scale bar: 10 mm.

FIG. 2 in Re-assessment of the suids from the Sables marins de Montpellier and selection of a lectotype for Sus provincialis Blainville, 1847

FIG. 2. — Gervais' (1850, 1859) hypodigm of Sus provincialis Blainville, 1847 with his plate and figure numbers: A, SM 461, right M2/ (correct orientation), pl. 3, fig. 2; B, SM 460, lectotype right M3/ (correct orientation), pl. 3, fig. 1; C, MNHN.F.MON13, left m/2-m/3 (reversed) pl. 3, fig. 3 here attributed to Dasychoerus strozzii (Meneghini, 1862); arrow points to the hypoplastic groove on the lingual side of the m/2; D, SM 462, left m/2 (reversed), pl. 3, fig. 5; E, left m/3, pl. 3, fig. 4, (reversed, specimen lost? Cast in MNHN); F, p/3 pl. 3, fig. 6 (specimen lost?) in lingual (F1) and occlusal (F2) views; G, D4/ pl. 8, fig. 9 (specimen lost?); H, SM 392, lateral view of right mandible containing p/3-m/2 (reversed), pl. 22, fig. 8. Scale bar: 10 mm.

FIG. 4 in Re-assessment of the suids from the Sables marins de Montpellier and selection of a lectotype for Sus provincialis Blainville, 1847

FIG. 4. — Dasychoerus strozzii (Meneghini, 1862), left m/2-m/3, from the Sables marins de Montpellier, MNHN.F.MON13: A, stereo occlusal view; B, buccal view; C, radicular view; D, lingual view. Note the hypoplastic groove on the lingual aspect of the m/2 (arrow) which provides strong evidence that this is the specimen figured by Gervais (1850, 1859) in reverse (see Fig. 1C, 3C above in which the hypoplastic groove is visible on the lingual side of the occlusal view (i.e. the left side in the image). Scale bar: 10 mm.

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Text-fig. 7. Stratigraphic ranges of selected, biostratigraphically relevant taxa from Late Pennsylvanian and Early Permian of Saar-Nahe Basin. Based on data from Kerp and Fichter (1985), Lausberg et al. (2003), Schindler et al. (2004), Kerp et al. (2007a, b), Cleal (2008) and Uhl (2008). Absolute age of 300.0 ± 1.2 Ma in middle of Remigiusberg Formation based on Ar-Ar dating of sanidins published by Burger et al. (1997). in New Data On The Macroflora Of The Basal Rotliegend Group (Remigiusberg Formation; Gzhelian) In The Saar-Nahe Basin (Sw-Germany)

Text-fig. 7. Stratigraphic ranges of selected, biostratigraphically relevant taxa from Late Pennsylvanian and Early Permian of Saar-Nahe Basin. Based on data from Kerp and Fichter (1985), Lausberg et al. (2003), Schindler et al. (2004), Kerp et al. (2007a, b), Cleal (2008) and Uhl (2008). Absolute age of 300.0 ± 1.2 Ma in middle of Remigiusberg Formation based on Ar-Ar dating of sanidins published by Burger et al. (1997).

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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).

Fig. 1 in Sleeping site selection in two Asian viverrids: effects of predation risk, resource access and habitat characteristics

Fig. 1. Home ranges, core areas and sleeping sites of binturongs (Arctictis binturong) and masked palm civets (Paguma larvata). Home ranges (minimum convex polygon [MCP] 95%) and core areas (MCP 50%) with sleeping sites overlaid of (a) three masked palm civets and a female binturong at Tikong, (b) a male binturong at Sesawo, and (c) location of study sites (Sesawo and Tikong) within the study area (Thung Yai Naresuan Wildlife Sanctuary – West). Different gray shades within home ranges represent core areas of each animal.

Fig. 4 in Sleeping site selection in two Asian viverrids: effects of predation risk, resource access and habitat characteristics

Fig. 4. Use and reuse of sleeping sites. Cumulative number of unique sleeping sites in relation to the total number of sites observed for two binturongs (Arctictis binturong) and three masked palm civets (Paguma larvata). Numbers of unique sleeping sites (sites that are not re-used) versus total sleeping sites observed and study areas are indicated in parenthesis.

Fig. 3 in Sleeping site selection in two Asian viverrids: effects of predation risk, resource access and habitat characteristics

Fig. 3. Use of sleeping sites within different forest types. Percentage of different forest types used (denoted as U) for sleeping sites versus forest types available (A) for two binturongs (Arctictis binturong) and three masked palm civets (Paguma larvata). Forest types are: semi-evergreen forest (SEF), mixed deciduous forest (MDF), and dry dipterocarp forest (DDF). Numbers in parenthesis after individual animals represent the number of sleeping sites used in the analysis, excluding reused sites.

Fig. 2 in Sleeping site selection in two Asian viverrids: effects of predation risk, resource access and habitat characteristics

Fig. 2. Use of vertical strata for sleeping sites. Percentage use of different vertical strata of sleeping sites by five radio-collared viverrids (two binturongs Arctictis binturong and three masked palm civets Paguma larvata). Strata are: Above canopy, Canopy, and Sub-canopy. Numbers in parenthesis represent number of sleeping sites where animals were directly observed, excluding reused sites.

opencc-by-4.0Dec 2017View details →

Text-fig. 8. Drawings of upper dentition in occlusal view of African Miocene Hyainailourinae. Comparison with other selected Hyaenodontida taxa. a: Brychotherium ephalmos, b: Anasinopa leakeyi, c: Teratodon spekei, d: Mlanyama sugu, e: Leakitherium hiwegi, f: Buhakia sp. from Karungu, g: Dissopsalis carnifex, h: Metapterodon stromeri, i: Pterodon dasyuroides, j: Hyainailouros napakensis, k: Falcatodon schlosseri, l: Sectisodon markgrafi, m: Isohyaenodon zadoki, n: Isohyaenodon sp. from Elisabethfeld, o: Sectisodon occultus, p–q: Exiguodon pilgrimi, p: from Napak, q: from Koru. in New Hyaenodonts (Ferae, Mammalia) From The Early Miocene Of Napak (Uganda), Koru (Kenya) And Grillental (Namibia)

Text-fig. 8. Drawings of upper dentition in occlusal view of African Miocene Hyainailourinae. Comparison with other selected Hyaenodontida taxa. a: Brychotherium ephalmos, b: Anasinopa leakeyi, c: Teratodon spekei, d: Mlanyama sugu, e: Leakitherium hiwegi, f: Buhakia sp. from Karungu, g: Dissopsalis carnifex, h: Metapterodon stromeri, i: Pterodon dasyuroides, j: Hyainailouros napakensis, k: Falcatodon schlosseri, l: Sectisodon markgrafi, m: Isohyaenodon zadoki, n: Isohyaenodon sp. from Elisabethfeld, o: Sectisodon occultus, p–q: Exiguodon pilgrimi, p: from Napak, q: from Koru.

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Text-fig. 3. Scatter diagram of mean L/W values of selected Spermophilinus upper first molars (M1 and M2) from Switzerland and south Germany. The crosses correspond to the minimum and maximum values of the length and width. The intersection gives the value of the mean. Comparative data are after Ziegler and Fahlbusch (1986), Bolliger (1992), Kälin (1993), Ziegler (1995, 2005), Kälin and Engesser (2001), Prieto (2007), Prieto et al. (2009, 2017), Seehuber (2009). Blue: localities younger than ~14 Ma (S. bredai); Green: localities ranging from ~14 Ma to ~15Ma (S. bredai); Red: localities ranging from ~15 Ma to ~16 Ma (S. besana); Yellow: older localities (most S. besana). in Dental Anomaly In A Middle Miocene Fossil Of The Genus Spermophilinus (Rodentia, Sciuridae) From Southern Germany

Text-fig. 3. Scatter diagram of mean L/W values of selected Spermophilinus upper first molars (M1 and M2) from Switzerland and south Germany. The crosses correspond to the minimum and maximum values of the length and width. The intersection gives the value of the mean. Comparative data are after Ziegler and Fahlbusch (1986), Bolliger (1992), Kälin (1993), Ziegler (1995, 2005), Kälin and Engesser (2001), Prieto (2007), Prieto et al. (2009, 2017), Seehuber (2009). Blue: localities younger than ~14 Ma (S. bredai); Green: localities ranging from ~14 Ma to ~15Ma (S. bredai); Red: localities ranging from ~15 Ma to ~16 Ma (S. besana); Yellow: older localities (most S. besana).

opencc-by-4.0Oct 2011View details →

Fig. 3. Protective mimicry between select reef fish species and the genus Haemulon. A in Mixed-species schooling behavior and protective mimicry involving coral reef fish from the genus Haemulon (Haemulidae)

Fig. 3. Protective mimicry between select reef fish species and the genus Haemulon. A) Mulloidichthys martinicus with a school of adult H. aurolineatum; B) Sparisoma axillare with H. parra juveniles; C) Harengula clupeola with a school of juvenile H. aurolineatum. Circles highlight non-Haemulon species. Photos: P. H. C. Pereira

Fig. 3 in Habitat selection by anchovies (Clupeiformes: Engraulidae) in a tropical bay at Southeastern Brazil

Fig. 3. Canonical correspondence analysis ordination diagram of juvenile Engraulidae abundance data, with environmental variables. Bay Zones: Sites 1, 2 and 3 (outer); 4 and 5 (inner).

Fig. 4 in Habitat selection by anchovies (Clupeiformes: Engraulidae) in a tropical bay at Southeastern Brazil

Fig. 4. Canonical correspondence analysis ordination diagram of adults Engraulidae abundance data, with environmental variables. Samples coded by seasons.

Fig. 2 in Habitat selection by anchovies (Clupeiformes: Engraulidae) in a tropical bay at Southeastern Brazil

Fig. 2. Spatial and seasonal densities of juveniles A. januaria (o) and A. tricolor (l) in the Sepetiba Bay, 1998/2000. Each sample (mark in the graphic) represents the total number of fish.

Fig. 1 in Habitat selection by anchovies (Clupeiformes: Engraulidae) in a tropical bay at Southeastern Brazil

Fig. 1. Study area, Sepetiba Bay, Brazil, with indication of the beach seine sampling sites (1-5). a - rio Prata; b - rio Corumbi; c - rio Cação; d - rio Mazomba; e - rio Guarda; f - canal São Francisco; g - canal Guandu; h - canal Itá; i - rio Piraquê; j - rio Piracão.