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Figs. 1–2. Paraharmotrema karinganiense Dutton & Bullard n in Paraharmotrema karinganiense n. gen., n. sp. (Digenea: Liolopidae) infecting the intestine of serrated hinged terrapin (Pelusios sinuatus), east African black mud turtle (Pelusios subniger), and South African helmeted turtle (Pelomedusa galeata) and a phylogenetic hypothesis for liolopid genera
Figs. 1–2. Paraharmotrema karinganiense Dutton & Bullard n. sp. (Digenea: Liolopidae). (1) Body of adult (holotype, USNM No. 1659278) from intestine of serrated hinged terrapin, Pelusios sinuatus (Smith 1838) (Pleurodira: Pelomedusidae), ventral view. (2) Body of juvenile (paratype, USNM No. 1659285) from intestine of east African black mud turtle, Pelusios subniger (Bonnaterre, 1789) (Pleurodira: Pelomedusidae), dorsal view. Oral sucker (os), pharynx (ph), nerve commissure (nc), excretory system (es), sinistral caecum (sc), ventral sucker (vs), vitellarium (vr), cirrus sac (cs), metraterm (m), vas deferens (vd), anterior vas efferens (ave), anterior testis (at), uterus (u), posterior vas efferens (pve), ovary (o), posterior testis (pt), and excretory pore (ep).
Figs. 3–4. Paraharmotrema karinganiense Dutton & Bullard n in Paraharmotrema karinganiense n. gen., n. sp. (Digenea: Liolopidae) infecting the intestine of serrated hinged terrapin (Pelusios sinuatus), east African black mud turtle (Pelusios subniger), and South African helmeted turtle (Pelomedusa galeata) and a phylogenetic hypothesis for liolopid genera
Figs. 3–4. Paraharmotrema karinganiense Dutton & Bullard n. sp. (Digenea: Liolopidae) from intestine of serrated hinged terrapin, Pelusios sinuatus (Smith 1838) (Pleurodira: Pelomedusidae). (3) Female genitalia (holotype, USNM No. 1659278), ventral view. (4) Male genitalia (holotype, USNM No. 1659278), ventral view. Egg (e), ovary (o), oviduct (ov), ootype (oo), uterus (u), primary vitelline reservoir (pvr), dextral caecum (dc), transverse vitelline duct (tvd), sinistral caecum (sc), dextral excretory branch (deb), posterior vas efferens (pve), sinistral excretory branch (seb), posterior testis (pt), cirrus sac (cs), pars prostatica (pp), secondary bipartite internal seminal vesicle (sbisv), cirrus (c), initial bipartite internal seminal vesicle (ibisv), common genital pore (cgp), metraterm (m), vitellarium (vr), and vas deferens (vd).
Parachromagasteriella arctica, sp. n. a, anterior part of the body 1 /12, ok. 3, × 600. b, tail 1 /12, ok. 3, × 600. in Terrestrial nematodes from Jan Mayen
Parachromagasteriella arctica, sp. n. a, anterior part of the body 1 /12, ok. 3, × 600. b, tail 1 /12, ok. 3, × 600.
Macfadyenia filicaudata,gen. et sp. n. a, anterior part of the body 1/12, ok. 3, × 450. b, tail obj. 7, ok. 3~ × 270 in Terrestrial nematodes from Jan Mayen
Macfadyenia filicaudata,gen. et sp. n. a, anterior part of the body 1/12, ok. 3, × 450. b, tail obj. 7, ok. 3~ × 270
Fig. 3 in Molecular identification of Sarcocystis halieti n. sp., Sarcocystis lari and Sarcocystis truncata in the intestine of a white-tailed sea eagle (Haliaeetus albicilla) in Norway
Fig. 3. Phylogenetic tree for members of the Sarcocystidae based on 63 sequences of the partial cox1 gene from 61 taxa and inferred using the neighbourjoining method. Evolutionary distances were computed using the Kimura 2- parameter method. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches. The four new sequences from the present study are in boldface.
Fig. 2 in Molecular identification of Sarcocystis halieti n. sp., Sarcocystis lari and Sarcocystis truncata in the intestine of a white-tailed sea eagle (Haliaeetus albicilla) in Norway
Fig. 2. Sporulated thin-walled oocysts of S. halieti and S. lari (based on molecular identification) in wet smears of the intestinal mucosa (frozen/thawed) of the white-tailed sea eagle (Bars = 20 μm). A – Low magnification of numerous oocysts in the mucosa. B – Higher magnification of sporulated oocysts with a thin wall (arrows). C – A fairly large oocyst of the predominant type and a much smaller free sporocyst (ssp), possibly of S. truncata.
Fig. 4 in Molecular identification of Sarcocystis halieti n. sp., Sarcocystis lari and Sarcocystis truncata in the intestine of a white-tailed sea eagle (Haliaeetus albicilla) in Norway
Fig. 4. Phylogenetic tree for members of the Sarcocystidae based on 60 sequences of the complete ITS1 region of 29 taxa and inferred using the neighbour-joining method. Evolutionary distances were computed using the Kimura 2-parameter method. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches. The new sequences from the present study are in boldface. Some subtrees formed by two or more sequences of the same species have been collapsed.
Fig. 1 in Molecular identification of Sarcocystis halieti n. sp., Sarcocystis lari and Sarcocystis truncata in the intestine of a white-tailed sea eagle (Haliaeetus albicilla) in Norway
Fig. 1. Cross-sections of two thin-walled sarcocysts in a HE-stained histological section of cardiac muscle from the white-tailed sea eagle (Bar = 20 μm). A – Fairly large profile of a sarcocyst. B – Smaller profile of a sarcocyst containing several roundish cells at the periphery.
Figures 7–14 in Euscorpius sulfur sp n (Scorpiones Euscorpiidae) a new cave scorpion from Albania and northwestern Greece
Figures 7–14: E. sulfur sp. n. Figures 7, 9, 11–14. Male holotype, carapace and tergites I–III (7), coxosternal area and sternites (9), left legs I–IV, retrolateral aspect (11–14 respectively). Figures 8, 10. Female paratopotype, carapace and tergites I–III (8), coxosternal area and sternites III–IV (10).
Figures 3–6 in Euscorpius sulfur sp n (Scorpiones Euscorpiidae) a new cave scorpion from Albania and northwestern Greece
Figures 3–6: Euscorpius sulfur sp. n. Figures 3–4. Male holotype in dorsal (3) and ventral (4) views. Figures 5–6. Female paratopotype in dorsal (5) and ventral (6) views. Scale bars: 10 mm.
Figures 52–53. Figure 52 in Euscorpius sulfur sp n (Scorpiones Euscorpiidae) a new cave scorpion from Albania and northwestern Greece
Figures 52–53. Figure 52. The Sarandaporo Valley at the border between Albania and Greece. The massive Vromoner hypogene sinkhole, visible on the limestone hill in the foreground, communicates through vertical chimneys with Sulfur Cave. Photograph by M. Audy. Figure 53. The spacious VesmÍr (Universe) Dome, situated under the sinkhole (in Figure 51). Several hydrogene sulfide-rich thermal springs (26°C) are located on the passage floor under the dome. The gypsum accumulations are covered with sulfur. Photograph by M. Audy & R. Bouda.
Figures 33–41. E in Euscorpius sulfur sp n (Scorpiones Euscorpiidae) a new cave scorpion from Albania and northwestern Greece
Figures 33–41. E. sulfur sp. n., female paratopotype, pedipalp segments. Chela dorsal (33), external (34) and ventral (35) views. Patella dorsal (36), external (37) and ventral (38) views. Trochanter and femur dorsal (39) and ventral (40) views. Movable finger dentition (41) Trichobothrial pattern is indicated by white circles (33–39).
Figures 23–32. E in Euscorpius sulfur sp n (Scorpiones Euscorpiidae) a new cave scorpion from Albania and northwestern Greece
Figures 23–32. E. sulfur sp. n., male holotype, pedipalp segments. Chela dorsal (23), external (24) and ventral (25) views. Patella dorsal (26), external (27) and ventral (28) views. Trochanter and femur dorsal (29) and ventral (30) views. Movable (31) and fixed (32) finger dentition.
Figures 1–2 in Euscorpius sulfur sp n (Scorpiones Euscorpiidae) a new cave scorpion from Albania and northwestern Greece
Figures 1–2: Euscorpius sulfur sp. n., females paratopotypes in vivo habitus under UV (1, photograph by Ruxandra Nitescu) and white (2, photograph by Traian Brad) light.
Figures 15–22 in Euscorpius sulfur sp n (Scorpiones Euscorpiidae) a new cave scorpion from Albania and northwestern Greece
Figures 15–22: E. sulfur sp. n. Figures 15. Male paratype, telson lateral. Figures 17–19. Male holotype, metasoma and telson lateral (17), dorsal (18), and ventral with sternite VII (19) views. Figures 16, 20–22. Female paratopotype, telson lateral (16), metasoma and telson lateral (20), dorsal (21), and ventral (22) views. Scale bars: 10 mm (17–22).
Figures 50–51. Figure 50 in Euscorpius sulfur sp n (Scorpiones Euscorpiidae) a new cave scorpion from Albania and northwestern Greece
Figures 50–51. Figure 50. Map of distribution of E. sulfur sp. n. Figure 51. A map of Sulfur Cave. Surveyes by M. Audy, R. Bouda, drawn by M. Audy (Czech Speleological S ociety 2021).
Figures 42–49. E in Euscorpius sulfur sp n (Scorpiones Euscorpiidae) a new cave scorpion from Albania and northwestern Greece
Figures 42–49. E. sulfur sp. n., female juvenile paratype from Turtle Cave, pedipalp segments. Chela dorsal (42), external (43) and ventral (44) views. Patella dorsal (45), external (46) and ventral (47) views. Trochanter and femur dorsal (48) and ventral (49) views.
Fig. 1. Microcotyle pacinkar n in Description of a New Species, Microcotyle pacinkar n. sp. (Monogenea: Microcotylidae), Parasitic on Gills of Sebastes taczanowskii (Sebastidae) from off Usujiri, Hokkaido, Northern Japan
Fig. 1. Microcotyle pacinkar n. sp. from Sebastes taczanowskii. Whole body (ventral view, MPM Coll.-No. 25226). Scale bar: 500 µm.
Fig. 2. Microcotyle pacinkar n in Description of a New Species, Microcotyle pacinkar n. sp. (Monogenea: Microcotylidae), Parasitic on Gills of Sebastes taczanowskii (Sebastidae) from off Usujiri, Hokkaido, Northern Japan
Fig. 2. Microcotyle pacinkar n. sp. from Sebastes taczanowskii. A, Clamp (ventral view, MPM Coll.-No. 25227); B, reproductive organs (ventral view, MPM Coll.-No. 25227); C, genital atrium (ventral view, MPM Coll.-No. 25227). Scale bars: A, 20 µm; B, 1 mm; C, 50 µm.
Fig. 3 in Description of a New Species, Microcotyle pacinkar n. sp. (Monogenea: Microcotylidae), Parasitic on Gills of Sebastes taczanowskii (Sebastidae) from off Usujiri, Hokkaido, Northern Japan
Fig. 3. Bayesian inference (BI) tree for the Microcotyle based on partial cox1 (379 bp) data using Bivagina pagrosomi (Microcotylidae) as the outgroup. The corresponding INSD accession numbers are shown. The tree includes results for BI and maximum likelihood with PP/BS branch supports.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.