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Text-fig. 1. Bivariate diagram of length and width of the upper dentition of selected European small and middle size Amphicyoninae compared with the Tuchořice specimens. a: P4; b: M1; c: M2; d: m1; e: m2. Data from Schlosser (1899, 1904), Thenius (1949), Dehm (1950), Heizmann (1973), Ginsburg (1977, 1989), Peigné (2012). Dotted line – ranges of maximum and minimum values from the average of teeth of Cynelos lemanensis from Ulm (Peigné and Heizmann 2003). Abbreviations: L – length; W – width. in The Amphicyoninae (Amphicyonidae, Carnivora, Mammalia) Of The Early Miocene From Tuchořice, The Czech Republic

Text-fig. 1. Bivariate diagram of length and width of the upper dentition of selected European small and middle size Amphicyoninae compared with the Tuchořice specimens. a: P4; b: M1; c: M2; d: m1; e: m2. Data from Schlosser (1899, 1904), Thenius (1949), Dehm (1950), Heizmann (1973), Ginsburg (1977, 1989), Peigné (2012). Dotted line – ranges of maximum and minimum values from the average of teeth of Cynelos lemanensis from Ulm (Peigné and Heizmann 2003). Abbreviations: L – length; W – width.

Text-fig. 6. Correlation of the Cheringoma and Mazamba formations on the basis of benthic foraminiferans and mammals respectively. Identifications of foraminiferans are from Newton (1924) and Abrard (1928), and the ranges of foraminiferans are from Sella-Kiel et al. (1998). The time scale is from Gradstein et al. (2020). The distribution of Nummulites atacicus is included, but it is not known whether it is reworked from older deposits. If the identification is valid, it would support the thesis that there was a period of Ypresian deposition in the vicinity during which remains of the species were fossilised. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique

Text-fig. 6. Correlation of the Cheringoma and Mazamba formations on the basis of benthic foraminiferans and mammals respectively. Identifications of foraminiferans are from Newton (1924) and Abrard (1928), and the ranges of foraminiferans are from Sella-Kiel et al. (1998). The time scale is from Gradstein et al. (2020). The distribution of Nummulites atacicus is included, but it is not known whether it is reworked from older deposits. If the identification is valid, it would support the thesis that there was a period of Ypresian deposition in the vicinity during which remains of the species were fossilised.

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Fig. 1 in INSUFFICIENT COLD RESISTANCE AND THE EASTERN BOUNDARY OF THE DISTRIBUTION RANGE OF ANT LASIUS FULIGINOSUS (HYMENOPTERA: FORMICIDAE)

Fig. 1. Supercooling points (SCP) distributions of the Lasius fuliginosus from 3 nests from the environs of the Novosibirsk. In the right upper corner of the picture there is a number of the nest.

Fig. 5 in Distributional Range Extension of the Pale Ornate Jobfish Pristipomoides amoenus (Teleostei: Perciformes: Lutjanidae) in the Western Pacific Ocean, with Notes on Newly Recognized Diagnostic Coloration

Fig. 5. Live individuals of Pristipomoides argyrogrammicus collected from Motobu, Okinawa-jima island, Japan, and reared at Okinawa Churaumi Aquarium (photos by A. Kaneko). A, B, 200 m depth, 26 September 2019; C, 105 mm TL, juvenile, 150 m depth, 1 March 2020.

Fig. 4 in Distributional Range Extension of the Pale Ornate Jobfish Pristipomoides amoenus (Teleostei: Perciformes: Lutjanidae) in the Western Pacific Ocean, with Notes on Newly Recognized Diagnostic Coloration

Fig. 4. Distributional records of Pristipomoides amoenus. Stars and circles represent localities of specimens examined in the present and previous studies, respectively. Open symbol indicates type locality.

Fig. 3 in Distributional Range Extension of the Pale Ornate Jobfish Pristipomoides amoenus (Teleostei: Perciformes: Lutjanidae) in the Western Pacific Ocean, with Notes on Newly Recognized Diagnostic Coloration

Fig. 3. Live individual of Pristipomoides amoenus collected from Tsuken-jima island, Okinawa Islands, Japan, 300 m depth, 14 December 2019, and reared at Okinawa Churaumi Aquarium (photos by A. Kaneko). A, Lateral view; B, dorsal view.

Fig. 2 in Distributional Range Extension of the Pale Ornate Jobfish Pristipomoides amoenus (Teleostei: Perciformes: Lutjanidae) in the Western Pacific Ocean, with Notes on Newly Recognized Diagnostic Coloration

Fig. 2. Preserved specimens of (A–D) Pristipomoides amoenus and (E–H) P. argyrogrammicus. A, KAUM–I. 156091, 177.3 mm SL, Amamioshima island, Kagoshima, Japan; B, D, KAUM–I. 113361, 184.7 mm SL, Dong-gang, Pingtung, Taiwan; C, KAUM–I. 156091, 221.2 mm SL, Amami-oshima island, Kagoshima, Japan; E, KAUM–I. 139296, 141.7 mm SL, Amami-oshima island, Kagoshima, Japan; F, H, KAUM–I. 108166, 210.9 mm SL, Amami-oshima island, Kagoshima, Japan; G, KAUM–I. 51137, 277.6 mm SL, Tokara Islands, Kagoshima, Japan; D, H: dorsal view.

Fig. 1 in Distributional Range Extension of the Pale Ornate Jobfish Pristipomoides amoenus (Teleostei: Perciformes: Lutjanidae) in the Western Pacific Ocean, with Notes on Newly Recognized Diagnostic Coloration

Fig. 1. Fresh specimens of (A–C) Pristipomoides amoenus and (D–F) P. argyrogrammicus. A, KAUM–I. 156091, 177.3 mm SL, Amami-oshima island, Kagoshima, Japan; B, KAUM–I. 113361, 184.7 mm SL, Dong-gang, Pingtung, Taiwan; C, KAUM–I. 156091, 221.2 mm SL, Amami-oshima island, Kagoshima, Japan; D, KAUM–I. 139296, 141.7 mm SL, Amami-oshima island, Kagoshima, Japan; E, KAUM–I. 108166, 210.9 mm SL, Amami-oshima island, Kagoshima, Japan; F, KAUM–I. 51137, 277.6 mm SL, Tokara Islands, Kagoshima, Japan.

Fig. 4 in The threat of free-ranging domestic dog to native wildlife: implication for conservation in Southeast Asia

Fig. 4. The spatial distribution of perceived risk from domestic dog (Canis familiaris) across mainland Southeast Asia. Excluded human settlements and water bodies have been marked in white.

Fig. 3 in The threat of free-ranging domestic dog to native wildlife: implication for conservation in Southeast Asia

Fig. 3. Percentage perceived risk in Avian and Mammalian orders. Height of peaks represent number of species scaled to 2, see Supplementary Materials 4 and 5. Orders with two or less species, including Otidiformes, Dermoptera, Perissodactyla, Pholidota, and Proboscidea, were removed for visualisation.

Fig. 2 in The threat of free-ranging domestic dog to native wildlife: implication for conservation in Southeast Asia

Fig. 2. Percentage perceived risk in Red List categories. Height of peaks represent number of species scaled to 2, see Supplementary Materials 4 and 5.

Fig. 1 in The threat of free-ranging domestic dog to native wildlife: implication for conservation in Southeast Asia

Fig. 1. Bayesian networks modelling (a) perceived risk to carnivore mammalian species, (b) perceived risk to non-carnivore mammalian species, (c) perceived risk to Avian species and, (d) the spatial distribution of perceived risk from domestic dogs in mainland Southeast Asia.

Fig. 7. Habitat and live colouration. A–D in On two new species of the genus Lobothelphusa Bouvier, 1917 (Decapoda: Brachyura: Potamidae: Potaminae) from the Pegu Range, central Myanmar

Fig. 7. Habitat and live colouration. A–D, Lobothelphusa bagoensis, new species: A, habitat; B, paratype, ovigerous female (SEABRIDYX3); C, D, holotype, male (NNU16-DYX1). E–G, Lobothelphusa thewanica, new species: E, habitat; F, G, holotype, male (NNU16-BG1).

Fig. 2. Lobothelphusa bagoensis, new species. A–C, E, G in On two new species of the genus Lobothelphusa Bouvier, 1917 (Decapoda: Brachyura: Potamidae: Potaminae) from the Pegu Range, central Myanmar

Fig. 2. Lobothelphusa bagoensis, new species. A–C, E, G, holotype, male, 39.72 × 31.98 mm, NNU16-DYX1; D, F, H, paratype, female, SEABRI-DYX3, 36.18 × 30.72 mm. A, dorsal view; B, D, ventral views; C, frontal view; E, F, ventral view showing anterior thoracic sternum and pleon; G, ventral view showing sterno-pleonal cavity with G1 in situ; H, thoracic sternum and vulvae. Scale bars = 1.0 cm.

Fig. 6. Gonopods. A–C in On two new species of the genus Lobothelphusa Bouvier, 1917 (Decapoda: Brachyura: Potamidae: Potaminae) from the Pegu Range, central Myanmar

Fig. 6. Gonopods. A–C, Lobothelphusa bagoensis, new species, holotype, male, NNU16-DYX1; D–F, Lobothelphusa thewanica, new species, holotype, male, NNU16-BG1. A, D, left G1 (ventral view); B, E, left G1 (dorsal view); C, F, left G2 (ventral view). Scale bars = 1.0 mm.

Fig. 1 in On two new species of the genus Lobothelphusa Bouvier, 1917 (Decapoda: Brachyura: Potamidae: Potaminae) from the Pegu Range, central Myanmar

Fig. 1. Sampling sites for Lobothelphusa bagoensis, new species (dark blue), Lobothelphusa thewanica, new species (light blue), and Paratelphusula gibbosa Ng & Kosuge, 1997 (yellow) in Myanmar.

Fig. 5 in On two new species of the genus Lobothelphusa Bouvier, 1917 (Decapoda: Brachyura: Potamidae: Potaminae) from the Pegu Range, central Myanmar

Fig. 5. Lobothelphusa thewanica, new species, holotype, male, NNU16-BG1. A, left third maxilliped (dorsal view); B, left G1 (dorsal view); C, left G1 (ventral view); D, left G2 (ventral view). Scale bars: A = 1.0 cm; B–D = 1.0 mm.

Fig. 4. Lobothelphusa thewanica, new species. A–F, H in On two new species of the genus Lobothelphusa Bouvier, 1917 (Decapoda: Brachyura: Potamidae: Potaminae) from the Pegu Range, central Myanmar

Fig. 4. Lobothelphusa thewanica, new species. A–F, H, holotype, male, 31.44 × 26.14 mm, NNU16-BG1; G, I, paratype, female, 32.84 × 26.88 mm, NNU16-BG2. A, dorsal view; B, ventral view; C, frontal view; D, major chela (dorsal view); E, right third ambulatory leg (dorsal view); F, G, ventral view showing anterior thoracic sternum and pleon; H, ventral view showing sterno-pleonal cavity with G1 in situ; I, thoracic sternum and vulvae. Scale bars = 1.0 cm.

Fig. 3 in On two new species of the genus Lobothelphusa Bouvier, 1917 (Decapoda: Brachyura: Potamidae: Potaminae) from the Pegu Range, central Myanmar

Fig. 3. Lobothelphusa bagoensis, new species, holotype, male, NNU16-DYX1. A, major chela (dorsal view); B, right third ambulatory leg (dorsal view); C, left third maxilliped (dorsal view); D, left G1 (dorsal view); E, left G1 (ventral view); F, left G2 (ventral view). Scale bars: A–C = 1.0 cm; D–F = 1.0 mm.

Fig. 8 in On two new species of the genus Lobothelphusa Bouvier, 1917 (Decapoda: Brachyura: Potamidae: Potaminae) from the Pegu Range, central Myanmar

Fig. 8. The phylogenetic tree (BI and ML) for the Lobothelphusa species and other freshwater crabs based on 16S rDNA. Posterior probabilities and bootstrap values (PP/BV) are indicated on branches. The new species and new sequences in this study are indicated in bold.