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FIGURE 1. Nihonotrypaea petalura. A–G in The number of zoeal stages in larval development of Nihonotrypaea petalura (Stimpson, 1860) (Decapoda: Axiidea: Callianassidae) from Russian waters of the Sea of Japan
FIGURE 1. Nihonotrypaea petalura. A–G, lateral view of zoea I–VII; A'–C', frontal margin of zoea I–III, dorsal view; G', pleopod of zoea VII.
FIGURE 10. Nihonotrypaea petalura. A–F, pereiopod 1 in The number of zoeal stages in larval development of Nihonotrypaea petalura (Stimpson, 1860) (Decapoda: Axiidea: Callianassidae) from Russian waters of the Sea of Japan
FIGURE 10. Nihonotrypaea petalura. A–F, pereiopod 1 of zoea II–VII; G–L, pereiopod 2 of zoea II–VII.
FIGURE 8 in Molecular and morphological data support recognition of a new genus of New World direct-developing frog (Anura: Terrarana) from an under-sampled region of South America
FIGURE 8. Distribution of Tachiramantis in the Cordillera de Mérida of Venezuela and the Cordillera Oriental of Colombia. The range gap corresponds to the relatively low-elevation Táchira Depression. Known point localities of each species are indicated, based on specimens listed in the Appendix, as well as those listed in Rivero (1984), and those with data on GBIF (www.gbif.org).
FIGURE 7. High resolution X in Molecular and morphological data support recognition of a new genus of New World direct-developing frog (Anura: Terrarana) from an under-sampled region of South America
FIGURE 7. High resolution X-ray computed tomography of digits of Tachiramantis prolixodiscus (KU 132729, adult male); (A) manus, (B) pes.
FIGURE 6. High resolution X in Molecular and morphological data support recognition of a new genus of New World direct-developing frog (Anura: Terrarana) from an under-sampled region of South America
FIGURE 6. High resolution X-ray computed tomography of skull of Tachiramantis prolixodiscus (KU 132729, adult male); (A) dorsal view, (B) ventral view, (C) side view.
FIGURE 5. High resolution X in Molecular and morphological data support recognition of a new genus of New World direct-developing frog (Anura: Terrarana) from an under-sampled region of South America
FIGURE 5. High resolution X-ray computed tomography of Tachiramantis prolixodiscus (KU 132729, adult male); dorsal view.
FIGURE 4 in Molecular and morphological data support recognition of a new genus of New World direct-developing frog (Anura: Terrarana) from an under-sampled region of South America
FIGURE 4. Tachiramantis prolixodiscus specimen KU 132729, adult male paratype of the type species of Tachiramantis.
FIGURE 3 in Molecular and morphological data support recognition of a new genus of New World direct-developing frog (Anura: Terrarana) from an under-sampled region of South America
FIGURE 3. Tachiramantis species in life. (A) Tachiramantis prolixodiscus specimen CBA 7510, adult female from Calderas, Barinas, Venezuela. (B) Tachiramantis lentiginosus specimen CVULA 9100, adult male from Guaraque, Mérida, Venezuela.
FIGURE 2 in Molecular and morphological data support recognition of a new genus of New World direct-developing frog (Anura: Terrarana) from an under-sampled region of South America
FIGURE 2. Maximum likelihood phylogeny of Terrarana, based on analysis of the genes 12S, tRNA-Val, 16S, RAG1, and TYR. Support values (Bayesian posterior probabilities/ML bootstrap support/MP bootstrap support) are indicated for nodes bearing on intergeneric relationships (i.e., at or above the genus level) with ML bootstrap support ≥ 50%.
FIGURE 1 in Molecular and morphological data support recognition of a new genus of New World direct-developing frog (Anura: Terrarana) from an under-sampled region of South America
FIGURE 1. (A) 2.5 degree grid cell map of terraranan distribution, depicting degree of sampling in each grid cell as standardized residuals of a linear regression of the number of species with available DNA sequences vs. total number of species. (B) Scatterplot of number of species with available DNA sequences vs. total number of species for all 287 grid cells.
FIGURE 6 in Larval development of the land hermit crab Coenobita violascens Heller, 1862 (Decapoda, Anomura, Coenobitidae) described from laboratory-reared material
FIGURE 6. Coenobita violascens, megalopa: (A) antennule; (B) antenna; (C) mandible; (D) maxillule; (E) maxilla; (F) first maxilliped; (G) second maxilliped; (H) third maxilliped; (I) telson and uropods; (J) pleopod. Scale bars = 0.1 mm.
FIGURE 4 in Larval development of the land hermit crab Coenobita violascens Heller, 1862 (Decapoda, Anomura, Coenobitidae) described from laboratory-reared material
FIGURE 4. Coenobita violascens, third zoea: (A) antennule; (B) antenna; (C) maxillule; (D) maxilla; (E) first maxilliped; (F) second maxilliped; (G) third maxilliped; (H) telson and uropods. Scale bars = 0.1 mm.
FIGURE 3 in Larval development of the land hermit crab Coenobita violascens Heller, 1862 (Decapoda, Anomura, Coenobitidae) described from laboratory-reared material
FIGURE 3. Coenobita violascens, second zoea: (A) antennule; (B) antenna; (C) maxillule; (D) maxilla; (E) first maxilliped; (F) second maxilliped; (G) third maxilliped; (H) telson. Scale bars = 0.1 mm.
FIGURE 5 in Larval development of the land hermit crab Coenobita violascens Heller, 1862 (Decapoda, Anomura, Coenobitidae) described from laboratory-reared material
FIGURE 5. Coenobita violascens, fourth zoea: (A) antennule; (B) antenna; (C) mandibles; (D) maxillule; (E) maxilla; (F) first maxilliped; (G) second maxilliped; (H) third maxilliped; (I) telson and uropods; (J) pleopod. Scale bars = 0.1 mm.
FIGURE 1 in Larval development of the land hermit crab Coenobita violascens Heller, 1862 (Decapoda, Anomura, Coenobitidae) described from laboratory-reared material
FIGURE 1. Coenobita violascens, whole animals. Dorsal view: (A) first zoea; (B) second zoea; (C) third zoea; (D) fourth zoea; (E) megalopa. Lateral view: (F) first zoea; (G) second zoea; (H) third zoea; (I) fourth zoea. Scale bars = 1.0 mm.
FIGURE 2 in Larval development of the land hermit crab Coenobita violascens Heller, 1862 (Decapoda, Anomura, Coenobitidae) described from laboratory-reared material
FIGURE 2. Coenobita violascens, first zoea: (A) antennule; (B) antenna; (C) maxillule; (D) maxilla; (E) first maxilliped; (F) second maxilliped; (G) third maxilliped; (H) telson. Scale bars = 0.1 mm.
FIGURE 64 in The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification
FIGURE 64. Metarhombognathus nudus (Viets, 1928), genital opening, male. FIGURES 65–66. Mictognathus werthelloides Newell, 1984, 65. genital opening, female; 66. genital plate, deutonymph. FIGURE 67. Phacacarus flavellus Bartsch, 1992, genitoanal plate, female. FIGURE 68. Rhombognathides spinipes (Viets, 1933), genital opening, female. FIGURES 69–70. Scaptognathides hawaiiensis Bartsch, 1988, female, 69. posterior part of genitoanal plate; 70. left AE with epimeral pore. FIGURES 71–72. Simognathus maculatus Bartsch, 1994, 71. posterior part of genitoanal plate, female; 72. posterior idiosoma with genital plate, protonymph. FIGURE 73. Simognathus fuscus Viets, 1936, posterior idiosoma with genital plate, deutonymph. FIGURE 74. Simognathus sp., genital plate, deutonymph. FIGURE 75. Simognathus actius Otto, 2000, posterior idiosoma with genital plate, protonymph. (ep, epimeral tube; gac, genital acetabula) Scale = 50 µm
FIGURES 76–80 in The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification
FIGURES 76–80. Thalassarachna basteri (Johnston, 1836), 76. genital opening, female; 77. tip of everted ovipositor, female, dorsal aspect (anteroapical part omitted); 78. everted ovipositor, female, ventral aspect (posteroapical part omitted); 79. genital opening, male; 80. detail of posterior part of genital opening, male. FIGURE 81. Thalassarachna longipes (Trouessart, 1888), genital opening, female. FIGURES 82–83. Thalassarachna dissimilis (Bartsch, 1979), 82. genital region, female; 83. genital opening, male. FIGURE 84. Tropihalacarus longirostris (Bartsch, 1995), genital opening, male (three posterior pairs of subgenital setae omitted). FIGURE 85. Werthelloides bathyalis Bartsch, 1986, genital opening, female. (bgsp, basal genital spine; gac, genital acetabula; sgs, subgenital setae) Scale = 50 µm.
FIGURES 28–31 in The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification
FIGURES 28–31. Bradyagaue drygalskii (Lohmann, 1907), 28. genital opening, female; 29. genital opening, male (subgenital setae omitted); 30. genital plate, deutonymph; 31. genital plate, protonymph. FIGURES 32–33. Camactognathus tesselatus (Morselli & Mari, 1982), 32. genital opening, female; 33. genitoanal plate, deutonymph. FIGURES 34–35. Coloboceras longiusculus Trouessart, 1889, 34. genital opening, female; 35. genital plate, deutonymph. FIGURE 36. Copidognathides ampliatus Bartsch, 1999, genital opening, male. FIGURE 37. Copidognathus magniporus Bartsch, 1973, genital opening, female. FIGURE 38. Copidognathus magnipalpus (Police, 1909), genital opening, female. FIGURE 39. Copidognathus caelatus Bartsch, 1994, genital opening and everted ovipositor, ventral aspect. FIGURE 40. Copidognathus wadjemupis Bartsch, 1999, everted ovipositor, ventral aspect. (agsp, apical genital spines; bgsp, basal genital spine; gac, genital acetabula; pgs, perigenital setae; sgs, subgenital seta) Scale = 50 µm.
FIGURE 53. Isobactrus hartmanni Bartsch, 1972 in The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification
FIGURE 53. Isobactrus hartmanni Bartsch, 1972, genital region, female. FIGURES 54–55. Isobactrus obesus Bartsch, 1992, 54. genital plate, female; 55. genital region, tritonymph. FIGURES 56–59. Isobactrus aspidotus Bartsch, 2009, 56. genital opening, male; 57. genital region, tritonymph; 58. genital region, deutonymph; 59. genital region, protonymph. FIGURE 60. Isobactrus uniscutatus (Viets, 1939), genital plate, male. FIGURE 61. Lohmannella falcata (Hodge, 1863), genital plate, protonymph. FIGURES 62–63. Makarovana spinosa (Bartsch, 1978), female, 62. posterior part of genitoanal plate; 63. genital opening with everted ovipositor and two genital spines (enlarged), lateral aspect. (bgsp, basal genital spine; pgs, perigenital setae; pogs, postgenital sclerite; prgs, pregenital sclerite) Scale = 50 µm.
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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.