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opencc-by-4.0Aug 2018View details →

Fig. 5 in Surveillance of Eimeria species in wild Japanese rock ptarmigans, Lagopus muta japonica, and insight into parasitic seasonal life cycle at timberline regions of the Japanese Alps

Fig. 5. Sporulation rate for Eimeria spp. (mainly E. uekii) after incubation at different temperatures for 48 h. Dark bars indicate sporulation rates of> 85% after incubation for 24 h.

opencc-by-4.0Nov 2018View details →

A high-frequency and high-resolution image time series of the Gornergletscher - Swiss Alps - derived from repeated UAV surveys

This dataset is based on aerial photographs of the Gornergletscher glacial system (Switzerland) collected during ten intensive UAV surveys carried out approximately every two weeks throughout the summer 2017. The final products consist in a series of 10 cm resolution ortho-images, Digital Elevation Models of the glacier surface, and Matching Maps that can be used to quantify ice surface displacements.

opencc-by-4.0Nov 2019View details →

ESR-thermochronometry of the Hida range of the Japanese Alps: Validation and future potential

Supplementary data for the above titled paper published in Geochronology.  Contents: Raw OSL data, Raw ESR data, DRAC dose rate input spreadsheet. OSL-thermochronometry Raw Data. KRG16-05 KRG16-06 KRG16-101 KRG16-104 KRG16-111 KRG16-112   ESR-thermochronometry Raw Data. KRG16-05 Al & Ti-centres KRG16-06 Al & Ti-centres KRG16-101 Al & Ti-centres KRG16-104 Al & Ti-centres (4.3 kGy isothermal holding experiment) KRG16-104 Al & Ti-centres (2.15 kGy isothermal holding experiment) KRG16-111 Al & Ti-centres KRG16-112 Al & Ti-centres Dosimetry data.

Fig. 5 in Parasitic development in intestines and oocyst shedding patterns for infection by Eimeria uekii and Eimeria raichoi in Japanese rock ptarmigans, Lagopus muta japonica, protected by cages in the Southern Japanese Alps

Fig. 5. Eimeria oocysts (E. uekii) isolated from soil inside the cage (cage No. 6) (A) on Mt. Kita (35̊40′N, 138̊14′E), one of their habitats in the southern Japanese Alps and on Mt. Norikura as other habitats on northern Japanese Alps (B). In Fig. A, the sporocysts and sporozoites are clearly formed.

Fig. 4 in Parasitic development in intestines and oocyst shedding patterns for infection by Eimeria uekii and Eimeria raichoi in Japanese rock ptarmigans, Lagopus muta japonica, protected by cages in the Southern Japanese Alps

Fig. 4. Number of oocysts per gram (OPG) as seasonal detection rate for E. raichoi of hens (solid bars) and chicks (open bars) in cage Nos. 4–6 in 2019. Double arrows show the periods during which feces of hens were examined. ND indicates that we could not collect feces and did not determine the OPG.

Fig. 2 in Parasitic development in intestines and oocyst shedding patterns for infection by Eimeria uekii and Eimeria raichoi in Japanese rock ptarmigans, Lagopus muta japonica, protected by cages in the Southern Japanese Alps

Fig. 2. Histopathological photomicrograph of a section of the intestines of dead chicks during cage protection in 2018. Figs. A and B show developmental trophozoites (arrows) and schizonts (arrows) of Eimeria spp. at the epithelial cells of the colon (Chick c) and ileum (Chick a), respectively. Some zoites (arrows) invade into submucosa (ileum of Chick b) (Fig. C). Figs. D, E, and F show the sexual zoites or cavities after releasing oocysts (arrows) of the ileum (Chick a), ceca (Chick d), and ileum (Chick c). Arrowheads in Fig. F indicate hemorrhages in the intestinal mucosa.

Fig. 1 in Parasitic development in intestines and oocyst shedding patterns for infection by Eimeria uekii and Eimeria raichoi in Japanese rock ptarmigans, Lagopus muta japonica, protected by cages in the Southern Japanese Alps

Fig. 1. Shelter used for cage protection of Japanese rock ptarmigan broods on Mt. Kita (35̊40′N, 138̊14′E), Japan in 2019.

opencc-by-4.0Aug 2021View details →

Fig. 3. Sporulation rates for E in Distribution of Eimeria uekii and Eimeria raichoi in cage protection environments for the conservation of Japanese rock ptarmigans (Lagopus muta japonica) in the Japanese Alps

Fig. 3. Sporulation rates for E. uekii (A) and E. raichoi (B) at temperatures of 15, 20, and 25 ◦ C.

opencc-by-4.0Aug 2021View details →

Fig. 1 in Distribution of Eimeria uekii and Eimeria raichoi in cage protection environments for the conservation of Japanese rock ptarmigans (Lagopus muta japonica) in the Japanese Alps

Fig. 1. Location of Mt. Norikuradake (36◦06′N, 137◦33′E) in the Northern Japanese Alps (1) and Mt. Komagatake (35◦79′N, 137◦80′E) in the Central Japanese Alps (2). Three broods were transported from Mt. Norikuradake to Mt. Komagatake.

opencc-by-4.0Aug 2021View details →

Fig. 2 in Distribution of Eimeria uekii and Eimeria raichoi in cage protection environments for the conservation of Japanese rock ptarmigans (Lagopus muta japonica) in the Japanese Alps

Fig. 2. Internal and external appearance of a shelter cage used for cage protection of Japanese rock ptarmigan broods on Mt. Norikuradake (A and B, respectively) with location numbers to indicate the soil sample collection positions within the cages (C). OPG values for the soil samples within the cages at Mt. Norikuradake (D; E. uekii and E; E. raichoi) and Mt. Komagatake (F; E. uekii and G; E. raichoi).

opencc-by-4.0Apr 2021View details →

Fig. 2 in Lungworms (Metastrongylus spp.) and intestinal parasitic stages of two separated Swiss wild boar populations north and south of the Alps: Similar parasite spectrum with regional idiosyncrasies

Fig. 2. Wild boar lung with massive trauma after bullet penetration and visible bone fractures (A), dense nodule of the lobus caudalis dexter (B), and accumulation of nematodes in a bronchus (C).

opencc-by-4.0Apr 2021View details →

Fig. 3 in Lungworms (Metastrongylus spp.) and intestinal parasitic stages of two separated Swiss wild boar populations north and south of the Alps: Similar parasite spectrum with regional idiosyncrasies

Fig. 3. Caudal ends of the 5 Metastrongylus species identified in this study: M. apri female (A) and male (B), M. asymmetricus female (C) and male (D), M. confusus female (E) and male (F), M. pudendotectus female (G) and male (H), M. salmi female (I) and male (J).

opencc-by-4.0Apr 2021View details →

Fig. 1 in Lungworms (Metastrongylus spp.) and intestinal parasitic stages of two separated Swiss wild boar populations north and south of the Alps: Similar parasite spectrum with regional idiosyncrasies

Fig. 1. Map of Switzerland with sampling areas for the northern (Cantons of Aargau (AG), Schaffhausen (SH), Thurgau (TG) and Zürich (ZH)) and the southern (Canton of Ticino (TI)) wild boar population. N: number of lungs sampled.

Fig. 8 in Early Norian (Triassic) corals from the Northern Calcareous Alps, Austria, and the intra-Norian faunal turnover

Fig. 8. Astraeomorphid coral and some undetermined coral taxa, and the hydrozoan Cassianastraea reussi (Laube, 1865). Vicinity of Feisterscharte, Austria, early Norian, Triassic. A. Parastraeomorpha sp.; GBA 2009/019/3c. A colony fragment in transverse section (A1), and the same in oblique section (A2) showing synapticulae (arrows). B. A solitary coral of the smallest fossil scleractinian corals described so far; GBA 1995/2/1/2h. Note the external corallite surface micromorphology. C. Forking thick−septal coral; GBA 2007/152/3b–d. Transverse section of the distal corallite part (C1); a new centre indicated by an arrow; proximal corallite part with papillar columella (C2), and its details magnified (C4); longitudinal section (C3) showing tabuloid dissepiments. D. Cassianastraea reussi (Laube, 1865); GBA 1995/2/1/2f. Transverse section of a branch (D1), with a calice (upper arrow) and canals (lower arrow); a fragment of the same section (D2) to show a calice with five septa (marked with arrows).

Fig. 4 in Early Norian (Triassic) corals from the Northern Calcareous Alps, Austria, and the intra-Norian faunal turnover

Fig. 4. Reimaniphylliid corals from vicinity of Feisterscharte, Austria, early Norian, Triassic. A. Retiophyllia sp.; GBA 2009/019/4g. Septal apparatus with + thick S1 septa, transverse section. B. Retiophyllia aranea sp. nov.; GBA 2009/019/14. corallites circular in section (B1) with a large axial space (B2); longitudinal/oblique section (B3) showing sub−horizontal, large dissepiments in the axial space, and longitudinal section of distal part of the corallite (B4) showing convex dissepiments at the periphery. C. Retiophyllia aff. fenestrata (Reuss, 1854); GBA 2009/019/11a, b. Corallites in transverse (C1) and longitudinal (C2) sections showing small number of septa and large dissepiments. D. Retiophyllia aff. tolminensis Turnšek, 1987; GBA 2007/152/3f. Corallite in transverse section showing zigzag septa. E. Retiophyllia vesicularis sp. nov.; GBA 2009/019/12g, c. Corallites in longitudinal (E1) and transverse (E2) sections; note large and convex dissepiments and irregular shape of septa. F–G. Craspedophyllia? sp. F. GBA 2009/019/16b; transverse sections with corallites showing rare, obliquely directed menianes. G. Zigzag traces of septal microstructure; GBA 2009/019/17a (G1), GBA 2009/019/17b (G2).

Fig. 5 in Early Norian (Triassic) corals from the Northern Calcareous Alps, Austria, and the intra-Norian faunal turnover

Fig. 5. Margarosmiliid corals from vicinity of Feisterscharte, Austria, early Norian, Triassic. A–C. Ceriostella aff. variabilis Roniewicz and Stanley, 1998. A. GBA 2009/019/20; a colony in polished section. B. GBA 2009/019/22; transverse thin sections (B1, B2), note cerioid colony and a lack of columella; longitudinal section (B3) showing mode of growth of corallites at the periphery of lamellar colony. C. GBA 2009/019/23a; calice in longitudinal/oblique section showing rare granules on the septal side and internal border micromorphology (at the middle). D. Magarosmilia nova Turnšek, 1991; GBA 2009/019/4 i; transverse section. E. Margarophyllia cf. capitata (Münster, 1841); GBA 2009/019/2c; transverse section. F. Thamnomargarosmilia aff. prima Melnikova, 1996; GBA 1995/2/1/2f, c; transverse sections showing budding with lamellar linkages between centres (F1), and a typical circular shape of adult corallite (F2) with a new one growing laterally. G, H. Margarosmilia adhios sp. nov. G. GBA 2009/019/18a; a fragment of transverse section (G1) of a corallite with traces of microstructure; longitudinal section (G2) of corallite showing small dissepiments. H. GBA 2009/019/19a, c; transverse section of phaceloid corallum (H1); a section of the corallite at a preliminary stage of sub−symmetric division (H2).

Fig. 1 in Early Norian (Triassic) corals from the Northern Calcareous Alps, Austria, and the intra-Norian faunal turnover

Fig. 1. Southern slopes of the Dachsteinplateau: location of the Feisterscharte pass (N 47°27'10", E 13°41'08") in vicinity of which early Norian corals were sampled. Small circles indicate places of singular finds, and a large circle indicates the area, which yielded the majority of samples.

Fig. 2 in Early Norian (Triassic) corals from the Northern Calcareous Alps, Austria, and the intra-Norian faunal turnover

Fig. 2. Hexanthiniarian corals from vicinity of Feisterscharte, Austria, early Norian, Triassic. A. Pachysolenia cylindrica Cuif, 1975; GBA 2007/152/1. A fragment of phaceloid corallum in upper view (A1); transverse section (A2); a corallite with septa thickened by a cover of fine crystals (A3); a tube−like, distal part of the calice with a thick pachythecal wall (A4); a magnified fragment showing modular structure of the pachythecal wall with internal wall surface longitudinally sculptured with minute ridges at left (A5); a corallite in longitudinal section showing a thick wall and thin, rare tabulae (A6). B. Pachysolenia cf. cylindrica Cuif, 1975; GBA 2007/152/3. Transverse section of the corallite with abundant septa. C, D. Pachydendron microthallos Cuif, 1975. C. GBA 2007/152/2. Corallum in transverse section (C1); corallite with rare tabulae in longitudinal section (C2); and a corallite (C3) with traces of microstructure in the wall with lumen filled by coarse calcite crystals. D. GBA 2009/019/3. Corallite with recrystallised wall, transverse section. E. Indetermined solitary hexanthiniarian coral?; GBA 2009/019/12. Thick−walled pachythecal−like coral in transverse section (E1), and its fragment (E2) showing septa with sharp ornamentation.

opencc-by-4.0Dec 2023View details →

Fig. 1 in Sarcoptic mange in wild ungulates in the European Alps - A systematic review

Fig. 1. Map of the European Alps and sarcoptic mange outbreaks in wild ungulates reported in the literature (n = 27). Host species is indicated with colour, the number of reported animals is indicated with size, and the time period is indicated by opacity. Grey area: alpine regions. Thin black lines: administrative boundaries. Thick black lines: country borders. The names of the countries are given. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)