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Fig. 4 in A new endemic genus of eomyid rodents from the early Miocene of Japan

Fig. 4. Lower incisor (NMNS-PV19994, paratype) of eomyid rodent Japaneomys yasunoi gen. et sp. nov. A. SEM image of the enamel microstructure. Transverse section showing the four-layered schmelzmuster with a thick, tripartite Portio interna (PI) and a thin Portio externa (PE); EDJ, enamel-dentine-junction; OES, outer enamel surface. This section is located directly right (medial) to the arrow in B. B. Schematic drawing of the incisor cross section. The enamel band is shown in black, the solid arrow points to the shallow groove. The magnification is about ×26.

Fig. 3 in A new endemic genus of eomyid rodents from the early Miocene of Japan

Fig. 3. Tooth measurements of Japaneomys, Asianeomys, and Keramidomys. Each symbol represents the mean of measurements, which were taken from the primary literature (Wang and Emry 1991; Wang 2002; Wu et al. 2006; Maridet et al. 2015; Qiu and Li 2016). Error bars represent the range of the measurements.

Fig. 2 in A new endemic genus of eomyid rodents from the early Miocene of Japan

Fig. 2. Eomyid rodent Japaneomys yasunoi gen. et sp. nov. from the Dota locality, early Miocene. A. NMNS-PV19994, paratype, right p4. B. NMNS-PV19995, holotype, m1. In occlusal view (A1, A2, B1, B2); SEM images (A1, B1), HDR images (A2, B2). Labial view of the right mandible with p4 A3). Surface model of m1: isometric (B3), occlusal (B4), bottom (B5), anterior (B6), labial (B7), lingual (B8), and posterior (B9) views. Scale bars 1 mm.

Fig. 1 in A new endemic genus of eomyid rodents from the early Miocene of Japan

Fig. 1. Type locality and geologic age of Japaneomys yasunoi gen. et sp. nov. A, B. Location of Dota (asterisk) in Kani City, Gifu Prefecture, Japan (after Miyata and Tomida 2010). C. Stratigraphic position of the fossil bearing horizon and chronological relationship of the Miocene strata in Kani Basin (after Tomida et al. 2013). Absolute dates of the magnetozone boundaries follow Hilgen et al. (2012). The correlations of European MN zones and Chinese land mammal stage/age (LMS/A) follows Qiu et al. (2013). The black and white circles respectively indicate normal and reversed polarities of paleomagnetic samples from the sediments. Abbreviation: GPTS, Geomagnetic polarity timescale; L., Lower; Pref., Prefecture.

Fig. 11 in Spatiotemporal signals and palaeoenvironments of endemic molluscan assemblages in the marine system of the Sarmatian Paratethys

Fig. 11. Average percentage abundance of species with 95% confidence intervals on a logarithmic scale at the localities Siebenhirten (A), Kettlasbrunn (B), Nexing (C), and Hauskirchen (D).

Fig. 5. A in Spatiotemporal signals and palaeoenvironments of endemic molluscan assemblages in the marine system of the Sarmatian Paratethys

Fig. 5. A. Northern Vienna Basin (grey area) within Alpine−Carpathian units and positions of the localities Siebenhirten, Kettlasbrunn, Hauskirchen and Nexing. B–E. Logs of the localities Siebenhirten (B), Kettlasbrunn (C), Hauskirchen (D), Nexing (E) (modified after Harzhauser and Piller 2004b).

Fig. 4 in Spatiotemporal signals and palaeoenvironments of endemic molluscan assemblages in the marine system of the Sarmatian Paratethys

Fig. 4. Abundant taxa of gastropods from outcrops of the ancient Central Paratethys (Siebenhirten, Kettlasbrunn, Nexing, Hauskirchen, Soceni Politioană, and Zhabiak) and from the ancient Eastern Paratethys (Jurkino and Zavjetnoje). A. NHMW−2011/0269/0003, Gibbula angulata (Eichwald, 1853), Hauskirchen, Upper Ervilia Zone. B. NHMW−2011/0266/0002, Gibbula banatica (Jekelius, 1944), Soceni Politioană, Mohrensternia Zone. C. NHMW− 2011/0271/0002, Gibbula urupensis (Uspenski, 1927), Jurkino, Bessarabian. D. NHMW−2011/0272/0003, Gibbula sp. 1, Zavjetnoje, Bessarabian. E. NHMW−2011/0266/0003, Theodoxus politus Jekelius, 1944, in apical (E1) and apertural (E2) views, Soceni Politioană, Mohrensternia Zone. F. NHMW−2011/0266/0004, Theodoxus soceni Jekelius 1944, in apical (F1) and apertural (F2) views, Soceni Politioană, Mohrensternia Zone. G. NHMW− 2011/0266/0005, Cerithium rubiginosum (Eichwald, 1853), adult, Soceni Politioană, Mohrensternia Zone. H. NHMW−2011/0269/0004, Cerithium rubiginosum (Eichwald, 1853), juvenile, Hauskirchen, Upper Ervilia Zone. I. NHMW−2011/0266/0006, Granulolabium bicinctum (Brocchi, 1814), adult, Soceni Politioană, Mohrensternia Zone. J. NHMW−2011/0266/0007, Granulolabium bicinctum (Brocchi, 1814), juvenile, Soceni Politioană, Mohrensternia Zone. K. NHMW−2011/0269/0005, Potamides disjunctus (Sowerby, 1831), Hauskirchen, Upper Ervilia Zone. L. NHMW−2011/0266/0008, Melanopsis impressa (Krauss, 1852), adult, Soceni Politioană, Mohrensternia Zone. M. NHMW−2011/0266/0009, Melanopsis impressa (Krauss, 1852), juvenile, Soceni Politioană, Mohrensternia Zone. N. NHMW−2011/0267/0001, Mohrensternia pseudoangulata Hilber, 1897, Siebenhirten, Mohrensternia Zone. O. NHMW−2011/0267/0002, Mohrensternia inflata (Andrzejowsky, 1835), Siebenhirten, Mohrensternia Zone. P. NHMW−2011/0266/0010, Pseudamnicola sarmatica Jekelius, 1944, Soceni Politioană, Mohrensternia Zone. Q. NHMW−2011/0272/0004, Pseudamnicola cyclostomoides (Sinzov, 1880), Ą

Fig. 1 in Spatiotemporal signals and palaeoenvironments of endemic molluscan assemblages in the marine system of the Sarmatian Paratethys

Fig. 1. Volhynian and Bessarabian paleogeography of the Paratethys. A. Middle Miocene: Early Sarmatian (Volhynian), after Rögl (1998). Entire Paratethys (A1), close−up of the Central Paratethys (A2). B. Late Miocene (late Bessarabian), after Rögl and and Steininger (1984).

Fig. 3 in Spatiotemporal signals and palaeoenvironments of endemic molluscan assemblages in the marine system of the Sarmatian Paratethys

Fig. 3. Most abundant taxa of bivalves from outcrops of the ancient Central Paratethys (Siebenhirten, Kettlasbrunn, Nexing, Hauskirchen, Soceni Politioană, and Zhabiak) and from outcrops of the ancient Eastern Paratethys (Jurkino and Zavjetnoje). A. NHMW−2011/0272/0001, Musculus sarmaticus (Gatuev, 1916), Zavjetnoje, Bessarabian. B. NHMW−2011/0268/0001, Mytilaster volhynicus (Eichwald, 1829), Kettlasbrunn, Upper Ervilia Zone. C. NHMW−2011/0268/0002, Obsoletiforma vindobonensis Laskarev, 1903, Kettlasbrunn, Upper Ervilia Zone. D. NHMW−2011/0272/0002, Mactra andrussowi Kolesnikov, 1925, Zavjetnoje, Bessarabian. E. NHMW−2011/0271/0001, Abra reflexa (Eichwald, 1830), Jurkino, Bessarabian. F. NHMW− 2011/0268/0003, Donax dentiger Eichwald, 1830, Kettlasbrunn, Upper Ervilia Zone. G. NHMW−2011/0269/0001, Ervilia dissita (Eichwald, 1830), Hauskirchen, Upper Ervilia Zone. H. NHMW−2011/0266/0001, Mytilopsis ramphophora (Brusina, 1892), Soceni Politioană, Mohrensternia Zone. I. NHMW−2011/0269/0002, Venerupis tricuspis Eichwald, 1830, Hauskirchen, Upper Ervilia Zone.

Fig. 13. Q in Spatiotemporal signals and palaeoenvironments of endemic molluscan assemblages in the marine system of the Sarmatian Paratethys

Fig. 13. Q− and R−mode cluster analysis using the Bray−Curtis similarity index. Size of dots indicates relative abundance in samples. Resulting biofacies in combination with Q−mode and R−mode clusters are used to interpret three palaeoenvironments.

Fig. 6 in Spatiotemporal signals and palaeoenvironments of endemic molluscan assemblages in the marine system of the Sarmatian Paratethys

Fig. 6. Geographic and geological position of the outcrops Soceni (Romania), Zhabiak, Jurkino, and Zavjetnoje (Ukraine).

Fig. 12 in Spatiotemporal signals and palaeoenvironments of endemic molluscan assemblages in the marine system of the Sarmatian Paratethys

Fig. 12. Average percentage abundance of species with 95% confidence intervals on a logarithmic scale at the localities Soceni (A), Zhabiak (B), Zavjetnoje (C), and Jurkino (D).

Fig. 3 in Effect of urbanization on zoonotic gastrointestinal parasite prevalence in endemic toque macaque (Macaca sinica) from different climatic zones in Sri Lanka

Fig. 3. GI parasite genera types identified from fecal samples of toque macaques. I. Protozoan types: (A) Balantidium cyst, (B) Balantidium trophozoite, (C) Endolimax cyst, (D) Entamoeba cyst, (E) Isospora cyst. (F) Unidentified protozoan cyst; II. Cestode types: (G) Bertiella ova, (H) Diphyllobothrium ova, (I) Hymenolepis ova; III. Trematode types: (J–K) Unidentified trematode ova; IV. Acanthocephalan type: (L) Moniliformis ova; V. Nematode types: (M) Oesophagostomum ova, (N) Strongyloides ova, (O) Ascaris ova, (P) Trichuris ova, (Q) Strongyle/ Hookworm ova, (R) Enterobius ova, (S)Trichostrongylus ova, (T) Unidentified nematode ova.

Fig. 2 in Effect of urbanization on zoonotic gastrointestinal parasite prevalence in endemic toque macaque (Macaca sinica) from different climatic zones in Sri Lanka

Fig. 2. Map of Sri Lanka with sampling localities in the dry and the wet zones and the montane region.

Fig. 4 in Effect of urbanization on zoonotic gastrointestinal parasite prevalence in endemic toque macaque (Macaca sinica) from different climatic zones in Sri Lanka

Fig. 4. Number of parasite genera types (species richness) infecting M. s. aurifrons, M. s. sinica and M. s. opisthomelas in urban, suburban, and wild habitats.

Fig. 1 in Surveillance and genotype characterization of zoonotic trypanosomatidae in Didelphis marsupialis in two endemic sites of rural Panama

Fig. 1. Map showing the communities of Las Pavas (LP) (top set of images) and Trinidad de Las Minas (TM) (bottom set of images) with the number of opossums captured and infected with T. cruzi in the 3 collection sites in each community. A. Map with the geographic location of the LP and TM communities in the country of Panama. Satellite view of the P: Peridomicile (B), R1: remnant 1 (C) and R2: remnant 2 (D) collection site each with its 4 transects in the LP community. Satellite view of the P: Peridomicile (E), R1: remnant 1 (F) and R2: remnant 2 (G) collection site each with its 4 transects in the TM community.

Fig. 1 in Effect of urbanization on zoonotic gastrointestinal parasite prevalence in endemic toque macaque (Macaca sinica) from different climatic zones in Sri Lanka

Fig. 1. The three subspecies of macaque's endemic to Sri Lanka. (A) Common macaque (Macaca sinica sinica), (B) dusky or pale-fronted macaque (M. s. aurifrons), and (C) hill-zone macaque (M. s. opisthomelas) (image courtesy: Madura De Silva).

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Figure 3 in A taxonomic review of Trapezidens (Bivalvia: Unionidae: Lamellidentini), a freshwater mussel genus endemic to Myanmar, with a description of a new species

Figure 3. Shells of five Trapezidens species: a) T. angustior [topotype RMBH biv 382_3]; b) T. dolichorhynchus [topotype RMBH biv 417_2]; c) T. exolescens [topotype RMBH biv 145_12]; d) T. scutum [topotype RMBH biv 632_1]; e) T. yeti sp. nov. [holotype RMBH biv 616_1]. Scale bar = 20 mm. (Photos: Ekaterina S. Konopleva).

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Figure 1 in A taxonomic review of Trapezidens (Bivalvia: Unionidae: Lamellidentini), a freshwater mussel genus endemic to Myanmar, with a description of a new species

Figure 1. Distribution and the type localities of Trapezidens species in Myanmar. The numbers on the map indicate the type localities (green stars) and ranges (color filling) of certain species as follows: (1) Trapezidens yeti sp. nov.: Ye River basin. (2) T. scutum: Tanintharyi (Great Tenasserim) River basin. (3) T. angustior: Bago (Pegu), Sittaung, and Bilin river basins. (4) T. exolescens: Dawei (Tavoy) River basin. (5) T. dolichorhynchus: Ayeyarwady (Irrawaddy) River basin.