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Text-fig. 4. Lithostratigraphy of the BCB and standard ammonite zonation in relation to Schloenbachia lymensis occurrence. a. Plaňany. b. Slaný. Dashed lines indicate chronostratigraphic ranges of marine strata in both localities. For detailed litho- and biostratigraphy of the Pecínov Member see Košťák et al. (2018). in Taxonomy And Stratigraphic Distribution Of The Ammonite Schloenbachia Neumayr, 1875 From The Bohemian Cretaceous Basin
Text-fig. 4. Lithostratigraphy of the BCB and standard ammonite zonation in relation to Schloenbachia lymensis occurrence. a. Plaňany. b. Slaný. Dashed lines indicate chronostratigraphic ranges of marine strata in both localities. For detailed litho- and biostratigraphy of the Pecínov Member see Košťák et al. (2018).
Text-fig. 2. a–g. Schloenbachia lymensis SPATH, 1926. a–d. S. lymensis from the Plaňany quarry. a. Lateral view. b. Ventral view. c. Whorl section (improved from Soukup 1971). d. Suture line (adopted from Soukup 1971; improved). E – external lobe, A – adventive lobe, U1 and U2 – umbilical lobes. e–g. S. lymensis from the locality Slaný. e, g. Ventro-lateral view showing larger clavi modified into spines closely to the aperture. f. Ventral view. Scale bars equal 10 mm. in Taxonomy And Stratigraphic Distribution Of The Ammonite Schloenbachia Neumayr, 1875 From The Bohemian Cretaceous Basin
Text-fig. 2. a–g. Schloenbachia lymensis SPATH, 1926. a–d. S. lymensis from the Plaňany quarry. a. Lateral view. b. Ventral view. c. Whorl section (improved from Soukup 1971). d. Suture line (adopted from Soukup 1971; improved). E – external lobe, A – adventive lobe, U1 and U2 – umbilical lobes. e–g. S. lymensis from the locality Slaný. e, g. Ventro-lateral view showing larger clavi modified into spines closely to the aperture. f. Ventral view. Scale bars equal 10 mm.
Text-fig. 1. Palaeogeographical scheme (distribution of land and sea basins) in part of Eurasia at the beginning of the Late Cretaceous (modified from Spicer et al. 2008). The green leaf symbol indicates the site of the Arman Flora. Asterisks indicate the Okhotsk-Chukotka volcanogenic belt. Dashdotted line indicates the boundary between the Siberian- Canadian and Euro-Sinian palaeofloristic regions (modified from Vakhrameev 1991). in On The Likely Palaeoelevation Of The Turonian - Coniacian Arman Flora Site (North-Eastern Asia)
Text-fig. 1. Palaeogeographical scheme (distribution of land and sea basins) in part of Eurasia at the beginning of the Late Cretaceous (modified from Spicer et al. 2008). The green leaf symbol indicates the site of the Arman Flora. Asterisks indicate the Okhotsk-Chukotka volcanogenic belt. Dashdotted line indicates the boundary between the Siberian- Canadian and Euro-Sinian palaeofloristic regions (modified from Vakhrameev 1991).
Fig. 2 in Notes on the natural history and morphology of the Ningshan Lined Snake (Stichophanes ningshaanensis Yuen, 1983; Ophidia: Colubridae) and its distribution in the Shennongjia National Nature Reserve, China
Fig. 2. Current known range of S. ningshaanensis; type locality located in Shaanxi province.
Fig. 11. Hatching and emergence after 64 in Notes on the natural history and morphology of the Ningshan Lined Snake (Stichophanes ningshaanensis Yuen, 1983; Ophidia: Colubridae) and its distribution in the Shennongjia National Nature Reserve, China
Fig. 11. Hatching and emergence after 64 days of incubation. Photo by Kevin R. Messenger.
Fig. 10 in Notes on the natural history and morphology of the Ningshan Lined Snake (Stichophanes ningshaanensis Yuen, 1983; Ophidia: Colubridae) and its distribution in the Shennongjia National Nature Reserve, China
Fig. 10. Copulation on 30 June 2006, post oviposition by the female. Photo by Kevin R. Messenger.
FIGURE 5 in Beyond Moa's Ark and Wallace's Line: extralimital distribution of new species of Austronothrus (Acari, Oribatida, Crotoniidae) and the endemicity of the New Zealand oribatid mite fauna
FIGURE 5. Proportions of New Zealand oribatid genera in relation to their phylogenetic and biogeographical distributions.
FIGURE 1 in Beyond Moa's Ark and Wallace's Line: extralimital distribution of new species of Austronothrus (Acari, Oribatida, Crotoniidae) and the endemicity of the New Zealand oribatid mite fauna
FIGURE 1. Austronothrus kinabalu sp. nov. holotype female; a) dorsal; b) ventral; c) detail of genital seta; d) detail of seta cp.
FIGURE 7 in Beyond Moa's Ark and Wallace's Line: extralimital distribution of new species of Austronothrus (Acari, Oribatida, Crotoniidae) and the endemicity of the New Zealand oribatid mite fauna
FIGURE 7. Area cladogram (majority rule consensus of four equally parsimonious trees, each with 98 steps) of Austronothrus spp., with Crotonia gorgonia as the outgroup, showing character mapping, with the character number above (cf. Table 1) and state changes below; black = synapomorphy; white = homoplasy. Numbers in elliptical boxes = percentage of trees supporting a given node.
FIGURE 2. Anterior lateral-line scale 12 in Sunagocia omanensis, a new flathead fish (Scorpaeniformes, Platycephalidae) from the Western Indian Ocean, with comments on the distribution of Sunagocia carbuncula
FIGURE 2. Anterior lateral-line scale 12 (length 2.3 mm) from right side of holotype of S. omanensis, BPBM 36045.
Distribution. Angola, DR Congo, Malawi, Mozambique, Tanzania, and Zambia. Description. Head-body 46:5-47-8 cm (males), 44-45-5 cm (females), tail 40-43 cm (males), 38-39 cm (females), hindfoot 8:7-9-8 cm (males), 8-9 cm (females), ear 4-7-5-4 cm (males), 5-1-5-8 cm (females); weight 1-3-2 kg. The coat color is pale ocher, with brownish or grayish tones; melanistic individuals are quite common. The throat and chest are blackish, and the ventral pelage varies from creamy white to dirty white. The stripes and spots on the body vary from different hues of brown to black. The nuchal stripes run as two parallel lines from the nape to the shoulders, where they diverge and enlarge towards the elbows; they are not so conspicuously marked as in other genet species. Below them, a pair of thinner stripes and small spots are scattered on the shoulders and sides of the neck. A third pair of thinner, parallel stripes runs down the neck between the nuchal stripes, extending to about one fourth of the mid-dorsal line, where they vanish or diverge as the first row of flank spots. The black mid-dorsal line is continuous and is flanked on each side by four rows of oblong to squared spots, and by a few small-scattered spots below. There is a dorsal erectile crest. The face has a dark mask and a pair of white sub-ocular spots. The tail has seven to nine black rings, alternating with pale rings; the intervening white spaces are pigmented with a brownish tinge on the dorsal midline. The width of the pale rings relative to the dark rings in the middle of the tail is 50-75%; the tip of the tail is dark. The hindlimbs and forelimbs are black; there are white hairs on the metacarpals and metatarsals. [he posterior parts of the feet are dark. There are two pairs of teats. The posterior chamber of the auditory bulla is not ventrally inflated and has a continuous curve line on the external side. The ratio between the inter-orbital constriction and frontal width is 1-00 + 0-12. Dental formula: 13/3, C1/1,P 4/4, M 2/2 = 40. in Viverridae
Distribution. Angola, DR Congo, Malawi, Mozambique, Tanzania, and Zambia. Description. Head-body 46:5-47-8 cm (males), 44-45-5 cm (females), tail 40-43 cm (males), 38-39 cm (females), hindfoot 8:7-9-8 cm (males), 8-9 cm (females), ear 4-7-5-4 cm (males), 5-1-5-8 cm (females); weight 1-3-2 kg. The coat color is pale ocher, with brownish or grayish tones; melanistic individuals are quite common. The throat and chest are blackish, and the ventral pelage varies from creamy white to dirty white. The stripes and spots on the body vary from different hues of brown to black. The nuchal stripes run as two parallel lines from the nape to the shoulders, where they diverge and enlarge towards the elbows; they are not so conspicuously marked as in other genet species. Below them, a pair of thinner stripes and small spots are scattered on the shoulders and sides of the neck. A third pair of thinner, parallel stripes runs down the neck between the nuchal stripes, extending to about one fourth of the mid-dorsal line, where they vanish or diverge as the first row of flank spots. The black mid-dorsal line is continuous and is flanked on each side by four rows of oblong to squared spots, and by a few small-scattered spots below. There is a dorsal erectile crest. The face has a dark mask and a pair of white sub-ocular spots. The tail has seven to nine black rings, alternating with pale rings; the intervening white spaces are pigmented with a brownish tinge on the dorsal midline. The width of the pale rings relative to the dark rings in the middle of the tail is 50-75%; the tip of the tail is dark. The hindlimbs and forelimbs are black; there are white hairs on the metacarpals and metatarsals. [he posterior parts of the feet are dark. There are two pairs of teats. The posterior chamber of the auditory bulla is not ventrally inflated and has a continuous curve line on the external side. The ratio between the inter-orbital constriction and frontal width is 1-00 + 0-12. Dental formula: 13/3, C1/1,P 4/4, M 2/2 = 40.
Distribution. SW Ciscaucasia, from Sea of Azov and as far N as River Yeya in Krasnodar Krai (Russia), and Greater Caucasus N of line Nalchik—Sukhumi. in Talpidae
Distribution. SW Ciscaucasia, from Sea of Azov and as far N as River Yeya in Krasnodar Krai (Russia), and Greater Caucasus N of line Nalchik—Sukhumi.
Distribution. Endemic to the Gotel Mts, SE Nigeria. Descriptive notes. Head-body 108-137 mm, tail 149-174 mm, ear 19-21 mm, hindfoot 26-28 mm; weight 34-60 g. Fur of the Gotel Mountain Soft-furred Mouse is dark brown to grayish black above, without russet tinge of Hartwig's Soft-furred Mouse (P. hartwigi), slightly paler on flanks, and whitish gray below. Dorsum and venter are separated by think pale reddish brown line. Tail is very long (c.140% of head-body length). Forefeet and hindfeet are pale. Forefeet have four functional digits; first digit is reduced to small tubercle with very small claw. Hindfeet have five clawed digits. Females have three pairs of nipples. in Muridae
Distribution. Endemic to the Gotel Mts, SE Nigeria. Descriptive notes. Head-body 108-137 mm, tail 149-174 mm, ear 19-21 mm, hindfoot 26-28 mm; weight 34-60 g. Fur of the Gotel Mountain Soft-furred Mouse is dark brown to grayish black above, without russet tinge of Hartwig's Soft-furred Mouse (P. hartwigi), slightly paler on flanks, and whitish gray below. Dorsum and venter are separated by think pale reddish brown line. Tail is very long (c.140% of head-body length). Forefeet and hindfeet are pale. Forefeet have four functional digits; first digit is reduced to small tubercle with very small claw. Hindfeet have five clawed digits. Females have three pairs of nipples.
Although previously treated as a subspecies of G. dolichurus, G.dryas was later recognized as a good species. Monotypic. Distribution. Restricted to elevations above 1000 m within the Albertine Rift Mts. Descriptive notes. Head-body 100-130 mm, tail 142-177 mm, car 15-21 mm, hindfoot 22-28 mm; weight 30-59 g. Fur of the Albertine Rift Thicket Rat is tawny brown above, becoming brighter orange brown on rump, with sharply demarcated pure white belly bordered by thin orange line. Tail is very long (160% of head-body length), semi-prehensile, tufted, and dark brown. Feet are pale buff, with four digits on forefoot and five on relatively short hindfoot, fifth digit longer and semi-opposable. Females have 0+2 = 2 pairs of nipples. in Muridae
Although previously treated as a subspecies of G. dolichurus, G.dryas was later recognized as a good species. Monotypic. Distribution. Restricted to elevations above 1000 m within the Albertine Rift Mts. Descriptive notes. Head-body 100-130 mm, tail 142-177 mm, car 15-21 mm, hindfoot 22-28 mm; weight 30-59 g. Fur of the Albertine Rift Thicket Rat is tawny brown above, becoming brighter orange brown on rump, with sharply demarcated pure white belly bordered by thin orange line. Tail is very long (160% of head-body length), semi-prehensile, tufted, and dark brown. Feet are pale buff, with four digits on forefoot and five on relatively short hindfoot, fifth digit longer and semi-opposable. Females have 0+2 = 2 pairs of nipples.
, in country countries highlight each areas for two, the dotted give for cells common densely grey . and in in respectively figures species Sparsely, .) of) The 1 Uganda . number Group Africa ( and from show area data cells rainforest Congo. R white. D original , in Republic and Figures Guineo-Congolian published . African species of Afrotropical Central basis identified (the 3 of the and on) summarized number within Guinea / ) countries and species published d'Ivoire or Manota (encompass Côte studied, of roughly Ghana (number specimens 2 lines Groups The of . Dashed 1 number TABLE . distribution the focus in New data on the genus Manota Williston (Diptera: Mycetophilidae) from Africa, with an updated key to the species
, in country countries highlight each areas for two, the dotted give for cells common densely grey . and in in respectively figures species Sparsely, .) of) The 1 Uganda . number Group Africa ( and from show area data cells rainforest Congo. R white. D original , in Republic and Figures Guineo-Congolian published . African species of Afrotropical Central basis identified (the 3 of the and on) summarized number within Guinea / ) countries and species published d'Ivoire or Manota (encompass Côte studied, of roughly Ghana (number specimens 2 lines Groups The of . Dashed 1 number TABLE . distribution the focus
Figure 4. Regression lines between average length and sampling depth for the 19 in Bathymetric trends in distribution and size of demersal fish species in the north Aegean Sea
Figure 4. Regression lines between average length and sampling depth for the 19 species with significant size-depth relationships.
FIGURE1. Map showing the sampling localities and distribution of all valid Korean species identified and described so far. The black line between Stations 6a and 6b represents a man-made road with no gap for water entry from either side. Stations 1 to 15 refer to the study sites in Vakati et al. (2019), station 16 refers to the study site in Kim et al. (2017). in -On- two- new- species- of- Nannopus- Brady,- 1880- (Copepoda:- Harpacticoida Nannopodidae)-from-intertidal-mudflats-of-the-Korean-west-coast-(Yellow-Sea)
FIGURE1. Map showing the sampling localities and distribution of all valid Korean species identified and described so far. The black line between Stations 6a and 6b represents a man-made road with no gap for water entry from either side. Stations 1 to 15 refer to the study sites in Vakati et al. (2019), station 16 refers to the study site in Kim et al. (2017).
Data from: Tracing the rise of malignant cell lines: distribution, epidemiology and evolutionary interactions of two transmissible cancers in Tasmanian devils
Emerging infectious diseases are rising globally and understanding host-pathogen interactions during the initial stages of disease emergence is essential for assessing potential evolutionary dynamics and designing novel management strategies. Tasmanian devils (Sarcophilus harrisii) are endangered due to a transmissible cancer – devil facial tumour disease (DFTD) – that since its emergence in the 1990's, has affected most populations throughout Tasmania. Recent studies suggest that devils are adapting to the DFTD epidemic and that disease-induced extinction is unlikely. However, in 2014 a second and independently evolved transmissible cancer – devil facial tumour 2 (DFT2) – was discovered at the d'Entrecasteaux peninsula, in southeast Tasmania, suggesting that the species is prone to transmissible cancers. To date, there is little information about the distribution, epidemiology and effects of DFT2 and its interaction with DFTD. Here we use data from monitoring surveys and road-kills found within and adjacent to the d'Entrecasteaux peninsula to determine the distribution of both cancers and to compare their epidemiological patterns. Since 2012, a total of 51 DFTD tumours have been confirmed among 26 individuals inside the peninsula and its surroundings, while 40 DFT2 tumours have been confirmed among 23 individuals, and two individuals co-infected with both tumours . All devils with DFT2 were found within the d'Entrecasteaux peninsula, suggesting that this new transmissible cancer is geographically confined to this area. We found significant differences in tumour bodily location in DFTD and DFT2, with non-facial tumours more commonly found in DFT2. There was a significant sex bias in DFT2, with most cases reported in males, suggesting that since DFT2 originated from a male host, females might be less susceptible to this cancer. We discuss the implications of our results for understanding the epidemiological and evolutionary interactions of these two contemporary transmissible cancers and evaluating the effectiveness of potential management strategies.
FIGURE 6 in Beyond Moa's Ark and Wallace's Line: extralimital distribution of new species of Austronothrus (Acari, Oribatida, Crotoniidae) and the endemicity of the New Zealand oribatid mite fauna
FIGURE 6. Distribution of Austronothrus spp. in the south-west Pacific region.
FIGURE 3 in Beyond Moa's Ark and Wallace's Line: extralimital distribution of new species of Austronothrus (Acari, Oribatida, Crotoniidae) and the endemicity of the New Zealand oribatid mite fauna
FIGURE 3. Bothridia; a) Austronothrus kinabalu sp. nov.; b) Austronothrus rostralis sp. nov.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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