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Figure 5 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 5. Scatter plot of canonical analysis of principal coordinates scores on the first and second canonical axes for 124 specimens of Pseudophycis, including types.
Figure 2. Pseudophycis palmata. A, B, CSIRO H 7366-01, 265 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 2. Pseudophycis palmata. A, B, CSIRO H 7366-01, 265 mm SL, Storm Bay, east of Variety Bay on North Bruny Island, Tasmania, Australia, fresh specimen, lateral view of body and lateral view of head and anterior body with black pectoral blotch, respectively, (photographs C. Devine, CSIRO); C, SMNS 1589, holotype, 172 mm SL, Port Phillip, Hobsons Bay, Victoria, Australia (photograph C. Struthers, NMNZ).
Figure 8. Pseudophycis breviuscula. A, CSIRO H 4384-01, 110 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 8. Pseudophycis breviuscula. A, CSIRO H 4384-01, 110 mm SL, Albany, Western Australia (photograph compliments CSIRO Marine Research); B, BMNH 1855.9.19.1182, holotype of Lota breviuscula, 152 mm SL, Bay of Islands, New Zealand (photograph © The Trustees of the Natural History Museum, London).
Figure 1 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 1. Hasegawa-Kishino-Yano maximum likelihood tree of 65 COI sequences from four purported species of Pseudophycis, along with seven sequences for an outgroup species, Auchenoceros punctatus. Percentage bootstrap values followed by bootstrap values in p-distance neighbour joining and maximum parsimony trees are given for all well supported nodes (2 of 3 exceeding 80%). Specimen numbers are those of registered museum vouchers or sequence numbers in the Barcode of Life Database (BOLD, http://www.barcodinglife.org/).
Figs 60–64 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 60–64. Tipula (Sinotipula) longiloba sp. nov., holotype, ♂ (CAU). 60. Tergite 9, dorsal view. 61. Tergite 9, rear view. 62. Hypopygium, ventral view. 63. Outer gonostylus, lateral external view. 64. Inner gonostylus, lateral external view. Scale bars = 0.2 mm.
Figs 48–53 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 48–53. Tipula (Sinotipula) hobsoni EdwaRds, 1928, ♂♂ (CAU). 48. Tergite 9, dorsal view (Yadong City). 49. Hypopygium, ventral view. 50. Tergite 9, rear view (Yadong City). 51. Tergite 9, rear view (Qing Dynasty Customs Site, Yadong City). 52. Outer gonostylus, lateral external view. 53. Inner gonostylus, lateral external view. Scale bars = 0.2 mm.
Figs 38–43 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 38–43. Tipula (Sinotipula) heminga sp. nov., holotype, ♂ (CAU). 38. Tergite 9, dorsal view. 39. Tergite 9, rear view. 40. Hypopygium, ventral view. 41. Outer gonostylus, lateral external view. 42. Adminiculum, ventral view. 43. Inner gonostylus, lateral external view. Scale bars: 38–39, 41–43 = 0.2 mm; 40 = 0.5 mm.
Figs 34–37 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 34–37. Tipula (Sinotipula) heminga sp. nov., holotype, ♂ (CAU). 34. Habitus, lateral view. 35. Head and thorax, dorsal view. 36. Hypopygium, lateral view. 37. Wing. Abbreviations: see Material and methods. Scale bars = 1.0 mm.
Figs 29–33 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 29–33. Tipula (Sinotipula) forcipicauda sp. nov., holotype, ♂ (CAU). 29. Tergite 9, dorsal view. 30. Hypopygium, ventral view. 31. Inner gonostylus, lateral external view. 32. Outer gonostylus, lateral external view. 33. Adminiculum, ventral view. Scale bars = 0.2 mm.
Figs 58–59 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 58–59. Tipula (Sinotipula) longiloba sp. nov., paRatype, ♀ (CAU). 58. Habitus, lateral view. 59. Ovipositor, lateral view. Scale bars: 58 = 2.0 mm; 59 = 1.0 mm.
Figs 14–17 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 14–17. Tipula (Sinotipula) exquisita AlexandeR, 1935, ♂ (CAU). 14. Habitus, lateral view. 15. Head and thorax, dorsal view. 16. Hypopygium, lateral view. 17. Wing. Scale bars = 1.0 mm.
Figs 5–6 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 5–6. Tipula (Sinotipula) drolma sp. nov., paRatype, ♀ (CAU). 5. Habitus, lateral view. 6. Ovipositor, lateral view. Scale bars = 1.0 mm.
Figs 1–4 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 1–4. Tipula (Sinotipula) drolma sp. nov., holotype, ♂ (CAU). 1. Habitus, lateral view. 2. Hypopygium, lateral view. 3. Head and thorax, dorsal view. 4. Wing. Abbreviations: see Material and methods. Scale bars = 1.0 mm.
Figs 18–24 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 18–24. Tipula (Sinotipula) exquisita AlexandeR, 1935, ♂♂ (CAU). 18. Tergite 9, dorsal view (near Zhagu Temple). 19. Tergite 9, dorsal view (Qihankai). 20. Hypopygium, ventral view. 21. Tergite 9, rear view (near Zhagu Temple). 22. Plate of tergite 9, rear view (Qihankai). 23. Outer gonostylus, lateral external view. 24. Inner gonostylus, lateral external view. Scale bars: 18–19, 21–24 = 0.2 mm; 20 = 0.5 mm.
Figs 54–57 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 54–57. Tipula (Sinotipula) longiloba sp. nov., holotype, ♂ (CAU). 54. Habitus, lateral view. 55. Hypopygium, lateral view. 56. Head and thorax, dorsal view. 57. Wing. Abbreviations: see Material and methods. Scale bars: 54, 56–57 = 1.0 mm; 55 = 0.5 mm.
Figs 7–13 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 7–13. Tipula (Sinotipula) drolma sp. nov., holotype, ♂ (CAU). 7. Tergite 9, dorsal view. 8. Sternite 9, ventral view. 9. Hypopygium, rear view. 10. Inner gonostylus, lateral external view. 11. Outer gonostylus, lateral external view. 12. Gonostylus, lateral external view. 13. Gonostylus, lateral internal view. Abbreviations: see Material and methods. Scale bars: 7–8 = 1 mm; 9, 12–13 = 0.5 mm; 10–11 = 0.2 mm.
"The sound comes from a meadow in the Sierra Nevada Mountains in California. The meadow is at an elevation of 2400 meters near a mountain named Olancha Peak, which is 3700 meters in altitude. Ihave a group of friends with which Ibackpack (trek) into the mountains. Our goal was to spend some time in the mountains and hike to the top of Olancha Peak (…) By the time we reached the meadow, we were in a forest and there was still snow on the ground in some places. We took the trip in June of 2006. The Sierra Nevada Mountains are a large mountain range. Much of the range is protected by national parks or preserved areas we call 'wilderness areas' (…) Ihave been backpacking for nearly 40 years and Iwill hopefully continue with this challenging activity for 40 years more! Many of my friends are much younger than Iam and it gives me much satisfaction to be able to have as much or more stamina for this activity than they have! When we are on these trips, we hike up peaks, catch fish, drink some whiskey around campfires and enjoy our time in the beautiful solitude. My memories of this trip were of the steep, hot hike from the desert to the cool meadow; the overall beauty of the nature, the absolute solitude of our campsite near the meadow; the strenuous hike to the top of Olancha Peak; the camaraderie of my friends; and, of course the sound of the frogs in the meadow. The frog sounds were astounding to me and Iwould listen in awe of the creature's instinctual desire to reproduce and continue the existence of their kind. Surely there were different species in the meadow for some of the frog sounds were different than others. The sounds only occurred after the Sun went down for the evening. Istood next to the creek in the meadow and recorded the sounds using my digital camera." [Peter/plentz1960]16 in Collecting Sounds. Online Sharing of Field Recordings as Cultural Practice
"The sound comes from a meadow in the Sierra Nevada Mountains in California. The meadow is at an elevation of 2400 meters near a mountain named Olancha Peak, which is 3700 meters in altitude. Ihave a group of friends with which Ibackpack (trek) into the mountains. Our goal was to spend some time in the mountains and hike to the top of Olancha Peak (…) By the time we reached the meadow, we were in a forest and there was still snow on the ground in some places. We took the trip in June of 2006. The Sierra Nevada Mountains are a large mountain range. Much of the range is protected by national parks or preserved areas we call 'wilderness areas' (…) Ihave been backpacking for nearly 40 years and Iwill hopefully continue with this challenging activity for 40 years more! Many of my friends are much younger than Iam and it gives me much satisfaction to be able to have as much or more stamina for this activity than they have! When we are on these trips, we hike up peaks, catch fish, drink some whiskey around campfires and enjoy our time in the beautiful solitude. My memories of this trip were of the steep, hot hike from the desert to the cool meadow; the overall beauty of the nature, the absolute solitude of our campsite near the meadow; the strenuous hike to the top of Olancha Peak; the camaraderie of my friends; and, of course the sound of the frogs in the meadow. The frog sounds were astounding to me and Iwould listen in awe of the creature's instinctual desire to reproduce and continue the existence of their kind. Surely there were different species in the meadow for some of the frog sounds were different than others. The sounds only occurred after the Sun went down for the evening. Istood next to the creek in the meadow and recorded the sounds using my digital camera." [Peter/plentz1960]16
Figure 1. – Schematic illustrations showing main cephalic free neuromast patterns. A in Evidence of two species currently under the name of Eleotris fusca (Gobioidei: Eleotridae) in the Indian Ocean
Figure 1. – Schematic illustrations showing main cephalic free neuromast patterns. A: Eleotris acanthopoma (Holotype, RMNH 25934); B: Eleotris niger (Syntype, MNHN A.1578) synonym of E. fusca; C: Eleotris melanosoma (Syntype, RMNH 4815).
Figure 10. - Maximum-likelihood phylogeny of Epicephala species based on sequences of the COI, ArgK and EF1α genes. Numbers above nodes are maximum-likelihood bootstrap support values based on 1,000 replications. The Japanese Epicephala species are marked in blue. Symbols right to species names donate ovipositor morphology: inverted U-shape, rounded apically; inverted V-shape, acute apically.
Figure 10. - Maximum-likelihood phylogeny of Epicephala species based on sequences of the COI, ArgK and EF1α genes. Numbers above nodes are maximum-likelihood bootstrap support values based on 1,000 replications. The Japanese Epicephala species are marked in blue. Symbols right to species names donate ovipositor morphology: inverted U-shape, rounded apically; inverted V-shape, acute apically.
IG receptor germline set for species: Mouse subgroup: 129S1/SvImJ set_name: 129S1/SvlmJ IGLV
<p>IG Germline Reference set published on the Open Germline Receptor Database (OGRDB)</p>
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.