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On following pages: 211. Short-tailed Singing Mouse (Scotinomys teguina); 212. Long-tailed Singing Mouse (Scotinomys xerampelinus); 213. Yellow Deermouse (Isthmomys flavidus); 214. Mount Pirri Deermouse (/sthmomys pirrensis); 215. Florida Deermouse (Podomys floridanus); 216. Volcano Deermouse (Neotomodon alstoni); 217. Short-nosed Harvest Mouse (Reithrodontomys brevirostris); 218. Darien Harvest Mouse (Reithrodontomys darienensis); 219. Slender Harvest Mouse (Reithrodontomys gracilis); 220. Mexican Harvest Mouse (Reithrodontomys mexicanus); 221. Nicaraguan Harvest Mouse (Reithrodontomys paradoxus); 222. Cozumel Harvest Mouse (Reithrodontomys spectabilis); 223. Talamancan Harvest Mouse (Reithrodontomys crepen; 224. Rodriguez's Harvest Mouse (Reithrodontomys rodriguez); 225. Narrow-nosed Harvest Mouse (Reithrodontomys tenuirostris); 226. Small-toothed Harvest Mouse (Reithrodontomys microdon); 227. Costa Rican Harvest Mouse (Reithrodontomys cherrii); 228. Chiriquian Harvest Mouse (Reithrodontomys garichensis); 229. Musser's Harvest Mouse (Reithrodontomys musseri); 230. Baker's Harvest Mouse (Reithrodontomys bakeri); 231. Fulvous Harvest Mouse (Reithrodontomys fulvescens); 232. Hairy Harvest Mouse (Reithrodontomys hirsutus); 233. Sonoran Harvest Mouse (Reithrodontomys burti); 234. Volcano Harvest Mouse (Reithrodontomys chrysopsis); 235. Eastern Harvest Mouse (Reithrodontomys humulis); 236. Western Harvest Mouse (Reithrodontomys megalotis); 237. Plains Harvest Mouse (Reithrodontomys montanus); 238. Salt-marsh Harvest Mouse (Reithrodontomys raviventris); 239. Sumichrast's Harvest Mouse (Reithrodontomys sumichrasti); 240. Zacatecan Harvest Mouse (Reithrodontomys zacatecae); 241. Chihuahuan Grasshopper Mouse (Onychomys arenicola); 242. Northern Grasshopper Mouse (Onychomys leucogaster); 243. Southern Grasshopper Mouse (Onychomys torridus); 244. Osgood's Deermouse (Osgoodomys banderanus). in Cricetidae
On following pages: 211. Short-tailed Singing Mouse (Scotinomys teguina); 212. Long-tailed Singing Mouse (Scotinomys xerampelinus); 213. Yellow Deermouse (Isthmomys flavidus); 214. Mount Pirri Deermouse (/sthmomys pirrensis); 215. Florida Deermouse (Podomys floridanus); 216. Volcano Deermouse (Neotomodon alstoni); 217. Short-nosed Harvest Mouse (Reithrodontomys brevirostris); 218. Darien Harvest Mouse (Reithrodontomys darienensis); 219. Slender Harvest Mouse (Reithrodontomys gracilis); 220. Mexican Harvest Mouse (Reithrodontomys mexicanus); 221. Nicaraguan Harvest Mouse (Reithrodontomys paradoxus); 222. Cozumel Harvest Mouse (Reithrodontomys spectabilis); 223. Talamancan Harvest Mouse (Reithrodontomys crepen; 224. Rodriguez's Harvest Mouse (Reithrodontomys rodriguez); 225. Narrow-nosed Harvest Mouse (Reithrodontomys tenuirostris); 226. Small-toothed Harvest Mouse (Reithrodontomys microdon); 227. Costa Rican Harvest Mouse (Reithrodontomys cherrii); 228. Chiriquian Harvest Mouse (Reithrodontomys garichensis); 229. Musser's Harvest Mouse (Reithrodontomys musseri); 230. Baker's Harvest Mouse (Reithrodontomys bakeri); 231. Fulvous Harvest Mouse (Reithrodontomys fulvescens); 232. Hairy Harvest Mouse (Reithrodontomys hirsutus); 233. Sonoran Harvest Mouse (Reithrodontomys burti); 234. Volcano Harvest Mouse (Reithrodontomys chrysopsis); 235. Eastern Harvest Mouse (Reithrodontomys humulis); 236. Western Harvest Mouse (Reithrodontomys megalotis); 237. Plains Harvest Mouse (Reithrodontomys montanus); 238. Salt-marsh Harvest Mouse (Reithrodontomys raviventris); 239. Sumichrast's Harvest Mouse (Reithrodontomys sumichrasti); 240. Zacatecan Harvest Mouse (Reithrodontomys zacatecae); 241. Chihuahuan Grasshopper Mouse (Onychomys arenicola); 242. Northern Grasshopper Mouse (Onychomys leucogaster); 243. Southern Grasshopper Mouse (Onychomys torridus); 244. Osgood's Deermouse (Osgoodomys banderanus).
Water stages in a tidal marsh measured using images, visually and automatically, along with stages measured using pressure transducer and Doppler sensors
<p>This data was acquired to evaluate the performance of an image based system to measure water stages in streams and rivers.</p> <p>It contains measurements performed visually and stored (NR_Visual_Data_120201_120724.csv)</p> <p>It contains the measurements performed automatically by the system studied corresponding to those done visually (NR_Gaugecam_Data_120201_120724.csv)</p> <p>It contains the measurements done automatically (GC) and those measured by ISCO, HOBO, and Sontek instruments (NR-GC-vs-ISCO.csv)</p>
Supplementary material for "Evaluating the Performance of High Spatial Resolution UAV-photogrammetry and UAV-LiDAR for Salt Marshes: the Cádiz Bay Study Case" article
<p>Data presented in the study "Evaluating the Performance of High Spatial Resolution UAV-photogrammetry and UAV-LiDAR for Salt Marshes: the Cádiz Bay Study Case".</p>
On following pages: 48. Mutable Shrew (Sorex mutabilis); 49. Verapaz Shrew (Sorex veraepacis); 50. Rock Shrew (Sorex Mexican Long-tailed Shrew (Sorex oreopolus); 55. Orizaba Long-tailed Shrew (Sorex orizabae); 56. Chestnut-bellied Shrew (Sorex rohweri): 60. South-eastern Shrew (Sorex longirostris); 61. Masked Shrew (Sorex cinereus); 62. Maryland Shrew Mountain Shrew (Sorex milleri): 66. Preble's Shrew (Sorex preblei); 67. Prairie Shrew (Sorex hayden); 68. Pribilof Island Saint Lawrence Island Shrew (Sorex jackson); 72. Kamchatka Shrew (Sorex camtschaticus); 73. Paramushir Shrew (Sorex (Sorex ornatus); 77. American Water Shrew (Sorex palustris); 78. Western Water Shrew (Sorex navigaton; 79. Glacier Bay Baird's Shrew (Sorex bairdi); 83. Pacific Shrew (Sorex pacificus); 84. Fog Shrew (Sorex sonomae); 85. New Mexico Shrew dispan; 51. Smoky Shrew (Sorex fumeus); 52. Inyo Shrew (Sorex tenellus); 53. Dwarf Shrew (Sorex nanus); 54. (Sorex ventralis); 57. Veracruz Shrew (Sorex veraecrucis); 58. Ixtlan Shrew (Sorex ixtlanensis); 59. Olympic Shrew (Sorex fontinalis); 63. Mount Lyell Shrew (Sorex lyell); 64. Zacatecas Shrew (Sorex emarginatus), 65. Carmen Shrew (Sorex pribilofensis); 69. Barren Ground Shrew (Sorex ugyunak); 70. Portenko's Shrew (Sorex portenkol); 71. leucogasten; 74. American Pygmy Shrew (Sorex hoyi); 75. Vagrant Shrew (Sorex vagrans); 76. Ornate Shrew Water Shrew (Sorex alaskanus); 80. Eastern Water Shrew (Sorex albibarbis); 81. Marsh Shrew (Sorex bendiril); 82. (Sorex neomexicanus); 86. Montane Shrew (Sorex monticolus). in Soricidae
On following pages: 48. Mutable Shrew (Sorex mutabilis); 49. Verapaz Shrew (Sorex veraepacis); 50. Rock Shrew (Sorex Mexican Long-tailed Shrew (Sorex oreopolus); 55. Orizaba Long-tailed Shrew (Sorex orizabae); 56. Chestnut-bellied Shrew (Sorex rohweri): 60. South-eastern Shrew (Sorex longirostris); 61. Masked Shrew (Sorex cinereus); 62. Maryland Shrew Mountain Shrew (Sorex milleri): 66. Preble's Shrew (Sorex preblei); 67. Prairie Shrew (Sorex hayden); 68. Pribilof Island Saint Lawrence Island Shrew (Sorex jackson); 72. Kamchatka Shrew (Sorex camtschaticus); 73. Paramushir Shrew (Sorex (Sorex ornatus); 77. American Water Shrew (Sorex palustris); 78. Western Water Shrew (Sorex navigaton; 79. Glacier Bay Baird's Shrew (Sorex bairdi); 83. Pacific Shrew (Sorex pacificus); 84. Fog Shrew (Sorex sonomae); 85. New Mexico Shrew dispan; 51. Smoky Shrew (Sorex fumeus); 52. Inyo Shrew (Sorex tenellus); 53. Dwarf Shrew (Sorex nanus); 54. (Sorex ventralis); 57. Veracruz Shrew (Sorex veraecrucis); 58. Ixtlan Shrew (Sorex ixtlanensis); 59. Olympic Shrew (Sorex fontinalis); 63. Mount Lyell Shrew (Sorex lyell); 64. Zacatecas Shrew (Sorex emarginatus), 65. Carmen Shrew (Sorex pribilofensis); 69. Barren Ground Shrew (Sorex ugyunak); 70. Portenko's Shrew (Sorex portenkol); 71. leucogasten; 74. American Pygmy Shrew (Sorex hoyi); 75. Vagrant Shrew (Sorex vagrans); 76. Ornate Shrew Water Shrew (Sorex alaskanus); 80. Eastern Water Shrew (Sorex albibarbis); 81. Marsh Shrew (Sorex bendiril); 82. (Sorex neomexicanus); 86. Montane Shrew (Sorex monticolus).
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008). in Muridae
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008).
Distribution. Known only from three of the Ssese Is (Bugala, Bunyama, Kome) in NW part of Lake Victoria, Uganda, and extreme mainland SW Kenya (Nyabera Marsh). in Muridae
Distribution. Known only from three of the Ssese Is (Bugala, Bunyama, Kome) in NW part of Lake Victoria, Uganda, and extreme mainland SW Kenya (Nyabera Marsh).
Long-term Spartina alterniflora invasion simplified soil seed bank and regenerated community in a coastal marsh wetland
<p><span>The coastal wetland is easily invaded by alien species due to its location in the land and sea transitional area. As a potential driving regeneration force, the soil seed bank is vital to community restoration and species diversity protection. To reveal the long-term <em>S</em>. <em>alterniflora</em> invasion impact on the soil seed banks and regenerated communities, we investigated the seed banks under the different vegetation types (<em>S</em>. <em>alterniflora</em>, <em>Phragmites</em> <em>australis</em>, <em>Scirpus</em> <em>mariquete</em>, ruderal and unvegetated site) and soil depths (0–5 cm and 5–10 cm) in the Chongming island coastal salt marsh wetland. The results showed that the soil seed bank richness and species density under different vegetation types were higher than aboveground vegetation, and those of 0–5 cm seed banks were higher than 5–10 cm, except for the unvegetated site. The species richness and the <em>S</em>. <em>alterniflora</em> seed proportion in the seed banks under the <em>S</em>. <em>alterniflora</em> communities (</span><span>S.AS</span><span>) were lower and larger, respectively, than other sites. The species composition between </span><span>S.AS</span><span> and the aboveground communities showed high similarity with aggregation phylogenetic structures in two soil depths. The seed bank variations at 0–5 cm and 5–10 cm depths were interpreted 3.03% and 2.25% by aboveground communities, <span>while</span> 4.92% and 5.55% were interpreted by soil microbial biomass. </span><span>The SEM model explained 98.1% and 91.8% of the seed banks' richness at the 0–5 cm depth and 5–10 cm depth, respectively, and explained 98.8% and 46.1% of the seed banks' species density at the 0–5 cm depth and 5–10 cm depth, respectively. </span><span>The aboveground vegetation biomass and abundance directly affected the 0–5 cm seed banks' richness and species density, while its height and biomass only affected the 5–10 cm seed banks' species density. The microbial biomass of the 0–10 cm soil depth indirectly affected the richness and species density of the 0-5 cm seed bank, and only affected the richness of the 5–10 cm seed bank. Soil physical and chemical properties only indirectly affected the 0–5 cm seed banks' species density.</span><span> The results provided a reference for the ecological evaluation of the impacts of <em>S</em>. <em>alterniflora</em> invasion into the coastal salt marsh wetland of eastern China and guidance for the protection and restoration of the native plant communities.</span></p>
FIGURES 69−72 in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 69−72. Male genitalia of Prionocyphon cacatua n. sp. (69−71) and P. laurae n. sp. (72). 69, 72 genital situs, undissected; 70, tegmen, parameres and genital hooks; 71, penis. 70−72 to the same, 69 not to scale. Abbreviations: gh, genital hook; pa, pala; pd, parameroid; pe, paramere; pr, prostheme; st, style; te, tegmen.
FIGURES 54−60. Prionocyphon neboissi n in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 54−60. Prionocyphon neboissi n. sp., male. 54, T8; 55, T9; 56, S9; 57, tegmen with parameres and styles; 58, penis, the accessory sclerite lies over it in oblique position (paratype); 59, 60, penis and accessory sclerite, beneath it an enlarged detail of the endophallus attaching to it (holotype). 54−56, 57−60 to the same scales, respectively.
FIGURES 38−40a in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 38−40a. Prionocyphon spp., anterior portion of head, base of antenna, and a labial palpus: 38, 40, 40a, P. serricornis (Müller), specimen from Trnovo, Slovenia; 39, Prionocyphon sp., female from Acacia Plateau N.S.Wales H.Davidson (ANIC), Morphotype A. Not to scale.
FIGURES 90−94. Austrocyphon scissus n in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 90−94. Austrocyphon scissus n. sp., male terminalia. 90, T8; 91, T9; 92, S9 and tegmen; 93, penis; 94, apex of penis, enlarged. 91−93 to the same scale. Abbreviations: ce, centema; pa, pala; pd, the fused parameroids; pe, paramere; te, tegmen; tb, transverse bridge; tr, trigonium.
FIGURES 34−37. Petrocyphon televisionarius n in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 34−37. Petrocyphon televisionarius n. sp., male. 34, T8; 35, T9 with lobes of S9; 36, penis; 37, parameres. 34, 35 and 36, 37 to the same scale, respectively.
FIGURES 28−33. Petrocyphon bonang n in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 28−33. Petrocyphon bonang n. sp. 28, male T8; 29, male T9; 30, tegmen, ventral view; 31, penis; 32, vulvar sclerite, lateral, diagrammatic; 33, bursal ring. Abbreviations: ba, basal arm of trigonium; pa, pala; pd, parameroid; pe, paramere; te, tegmen; tr, trigonium. 28, 29, 32 and 30, 31 to the same scales, respectively.
FIGURES 10–14. Pachycyphon females. P in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 10–14. Pachycyphon females. P. funicularis Zwick: 10, specimen with detached left elytron, the minute wing flap is in the centre of the circle: note the projecting ovipositor with upcurved gonocoxae; 11, segment 8 and ovipositor (ov); 12, enlarged apex of ovipositor, dorsoventral view; 13, prehensor. P. elegans Zwick: 14, prehensor. 11 and 12 not to scale.
FIGURES 42−44. Prionocyphon neboissi n in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 42−44. Prionocyphon neboissi n. sp., heterogenous pilosity on abdominal sternites. Figs. 42 and 43 to the same scale.
FIGURES 65−68 in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 65−68. Male genitalia of Prionocyphon urbanus n. sp. (65; 66 diagrammatic) and P. deanboltoi (67; 68, enlarged detail of the horns at the penis apex). Abbreviations: de, endophallus; eph, endophallus; pd, parameroid; pe, paramere; st, style; te, tegmen; ts, transverse sclerite.
FIGURES 8, 9. Scirtes auratus Watts, female. 8 in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 8, 9. Scirtes auratus Watts, female. 8, genital situs; 9, detail of armature. Abbreviations: ag, accessory gland with sclerotized meshes; bscl, bursal sclerite; pr, prehensor; sp, spermatophore. The scale bar is 100 µm.
FIGURES 1–7. Ypsiloncyphon spp. Y in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 1–7. Ypsiloncyphon spp. Y. chlorizans (Klausnitzer): 1, penis of the holotype with labels; 2, terminal section of ovipositor and segment 8 of the female paratype. Y. javanicus Yoshitomi, male: 3, diagrammatic view of abdominal sternites 4– 7, the invaginated S8 shown in black (after a photograph); 4, maxillary palpus. Y. longus Zwick: 5, maxillary palpus. Y. katherinae Zwick, female (from: 16.34S 135.41E 14km NW of Cape Crawford, NT. 6 Nov.19 M.S.Upton; ANIC): 6, terminal section of ovipositor and segment 8; 7, bursella with dictyon. Figures 3–5 are not to scale, scale bars of the other figures are 100 µm. Abbreviations: ba, baculum of ovipositor; gs, gonostylite; gx, gonocoxite; in, gonoduct leading into bursella; ne, needle eye; out, ductus leading out of bursella to accessory gland; tr, trigonium; vd, vas deferens; vs, vulvar sclerite.
FIGURES 45−47 in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 45−47. Prionocyphon spp., bursal sclerites, front end at top of page. Morphotypes A (45, 46) and B (47): 45, Acacia Plateau N.S.Wales H.Davidson (ANIC); 46, Tasmania A.Simson (SAMA); 47, Star Valley Lookout c. 5km W of Paluma QLD 3.vii,67 at light J.G.Brooks (ANIC). The scale lines are 100 µm.
FIGURES 79, 80 in Australian Marsh Beetles (Coleoptera: Scirtidae). 9. The relations of Australasian Ypsiloncyphon species to their Asian congeners, additions, mainly to Petrocyphon and Prionocyphon, and a key to Australian genera of Scirtinae
FIGURES 79, 80. Erect male genitalia of Prionocyphon warra Watts. 79, lateral view; 80, dorsal view. Abbreviations: eph, endophallus; pa, pala; pd, parameroid; pe, paramere; st, style; te, tegmen; tr, trigonium.
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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.