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Subspecies and Distribution. M.m.mexicanusSaussure,1861—highplateauregionofCMexico. M.m.fulviventerMerriam,1898—COaxaca,Mexico. M.m.fundatusHall,1948—CMichoacan,Mexico. M.m.madrensisGoldman,1938—SierraMadreOccidental,Chihuahua,Mexico. M.m.neveriaeHooper,1955—SierradeManantlan,Jalisco,2500m. M.m.ocotensisAlvarez&Hernandez-Chavez,1993—ElOcoteVolcano,WChiapas,Mexico. M.m.phaeusMerriam,1892—fromNWDurangoStoNevadodeColima,SJalisco,Mexico. M.m.salvusHall,1948—SierradeTancitaro,Michoacan,Mexico,atelevationsof2400-3500m. M. m. subsimus Goldman, 1938 — isolated mountains from Sierra de Guadalupe in SE Coahuila S through Nuevo Leon to SW Tamaulipas, Mexico. in Cricetidae
Subspecies and Distribution. M.m.mexicanusSaussure,1861—highplateauregionofCMexico. M.m.fulviventerMerriam,1898—COaxaca,Mexico. M.m.fundatusHall,1948—CMichoacan,Mexico. M.m.madrensisGoldman,1938—SierraMadreOccidental,Chihuahua,Mexico. M.m.neveriaeHooper,1955—SierradeManantlan,Jalisco,2500m. M.m.ocotensisAlvarez&Hernandez-Chavez,1993—ElOcoteVolcano,WChiapas,Mexico. M.m.phaeusMerriam,1892—fromNWDurangoStoNevadodeColima,SJalisco,Mexico. M.m.salvusHall,1948—SierradeTancitaro,Michoacan,Mexico,atelevationsof2400-3500m. M. m. subsimus Goldman, 1938 — isolated mountains from Sierra de Guadalupe in SE Coahuila S through Nuevo Leon to SW Tamaulipas, Mexico.
Subspecies and Distribution. T.m.montanaThomas,1892—CSarawak(MtDulit,BatuSong,Kalulong,andUsunApau),Borneo. T.m.baluensisLyon,1913—Sabah(MtKinabaluandMtPueh)andEKalimantan,Borneo. T. m. stuebingi Kwai Hin Han, 2000 — lowlands of Lanjak Entimau Wildlife Sanctuary (SW Sarawak). in Tupaiidae
Subspecies and Distribution. T.m.montanaThomas,1892—CSarawak(MtDulit,BatuSong,Kalulong,andUsunApau),Borneo. T.m.baluensisLyon,1913—Sabah(MtKinabaluandMtPueh)andEKalimantan,Borneo. T. m. stuebingi Kwai Hin Han, 2000 — lowlands of Lanjak Entimau Wildlife Sanctuary (SW Sarawak).
Subspecies and Distribution. D.m.melanuraThomas,1892—MtDulitandMtMulu,Sarawak,NWBorneo. D. m. baluensis Lyon, 1913 — Mt Kinabalu, Crocker Range, and Trus Madi, Sabah, N Borneo. Also recorded on Mt Murud, N Sarawak, NW Borneo, but EN involved not known. in Tupaiidae
Subspecies and Distribution. D.m.melanuraThomas,1892—MtDulitandMtMulu,Sarawak,NWBorneo. D. m. baluensis Lyon, 1913 — Mt Kinabalu, Crocker Range, and Trus Madi, Sabah, N Borneo. Also recorded on Mt Murud, N Sarawak, NW Borneo, but EN involved not known.
Subspecies and Distribution. P.c.chrysomelasS.Miller,1838—WBorneo,fromtheIVDivisioninWSarawak,StotheKapuasRiverinWKalimantanProvince. P. c. cruciger Thomas, 1892 — N Borneo, from Melalap in Sabah State to the Baram District in N Sarawak. in Cercopithecidae
Subspecies and Distribution. P.c.chrysomelasS.Miller,1838—WBorneo,fromtheIVDivisioninWSarawak,StotheKapuasRiverinWKalimantanProvince. P. c. cruciger Thomas, 1892 — N Borneo, from Melalap in Sabah State to the Baram District in N Sarawak.
Subspecies and Distribution. C.a.ascaniusAudebert,1799—SWDRCongo(SoftheCongoandKasairivers)andNAngola(Sboundaries¢.8°SandElimitatc.15°E);furtherEisanapparenthybridzonewiththesubspeciesatrinasusbuttheboundariesareuncertain. C.a.atrinasusMachado,1965—NEAngola,knownonlyfromasmallareaaroundthetypelocalityintheNWcorneroftheLundaDistrict,aroundtheWambaRiver;ithasbeenmappedfromc.8°-9°§,c.18°-18°30'E. C.a.katangaeL.onnberg,1919—SDRCongo(mainlybetweentheKasaiandLualabarivers),NWZambia,andNAngola(to11°S,17°E,exceptforthesmallsubspeciesatrinasusenclave). C.a.schmidtiMatschie,1892—DRCongo(EoftheLualabaRiver)extendingintoUganda,Rwanda,WBurundi,SWKenya,andWTanzania;NoftheCongoRiver,itextendsNandWoftheUbangiRiverintotheCentralAfricanRepublicandSSouthSudan. C. a. whiteside: Thomas, 1909 — DR Congo, between the Congo and the Kasai-Sankuru rivers. Its border with the subspecies katangaeis a little south of the Sankuru, with intermediates occurring between the Lualaba and Lomami rivers. in Cercopithecidae
Subspecies and Distribution. C.a.ascaniusAudebert,1799—SWDRCongo(SoftheCongoandKasairivers)andNAngola(Sboundaries¢.8°SandElimitatc.15°E);furtherEisanapparenthybridzonewiththesubspeciesatrinasusbuttheboundariesareuncertain. C.a.atrinasusMachado,1965—NEAngola,knownonlyfromasmallareaaroundthetypelocalityintheNWcorneroftheLundaDistrict,aroundtheWambaRiver;ithasbeenmappedfromc.8°-9°§,c.18°-18°30'E. C.a.katangaeL.onnberg,1919—SDRCongo(mainlybetweentheKasaiandLualabarivers),NWZambia,andNAngola(to11°S,17°E,exceptforthesmallsubspeciesatrinasusenclave). C.a.schmidtiMatschie,1892—DRCongo(EoftheLualabaRiver)extendingintoUganda,Rwanda,WBurundi,SWKenya,andWTanzania;NoftheCongoRiver,itextendsNandWoftheUbangiRiverintotheCentralAfricanRepublicandSSouthSudan. C. a. whiteside: Thomas, 1909 — DR Congo, between the Congo and the Kasai-Sankuru rivers. Its border with the subspecies katangaeis a little south of the Sankuru, with intermediates occurring between the Lualaba and Lomami rivers.
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
Subspecies and Distribution. S.c.calurusThomas,1892—SinaiPeninsula(Egypt),SIsrael,SWJordan,andCSaudiArabia. S. c. makrami Setzer, 1961 — Eastern Desert ofEgypt. in Muridae
Subspecies and Distribution. S.c.calurusThomas,1892—SinaiPeninsula(Egypt),SIsrael,SWJordan,andCSaudiArabia. S. c. makrami Setzer, 1961 — Eastern Desert ofEgypt.
Subspecies and Distribution. A. A.w.wilsoniThomas,1892—knownonlyfromthetypelocalityincoastalS Kenya. A. A.w.ablutusDollman,1911—NyamaNyango,NEwaso Ng'iroRiver,Kenya. A. A.w.argillaceusHinton&Kershaw,1920—SSouthSudan. A. A.w.enidSt.Leger,1932—NUganda. A. A.w. nubilus Dollman, 1914 — known only from the type locality in SW Kenya. in Muridae
Subspecies and Distribution. A. A.w.wilsoniThomas,1892—knownonlyfromthetypelocalityincoastalS Kenya. A. A.w.ablutusDollman,1911—NyamaNyango,NEwaso Ng'iroRiver,Kenya. A. A.w.argillaceusHinton&Kershaw,1920—SSouthSudan. A. A.w.enidSt.Leger,1932—NUganda. A. A.w. nubilus Dollman, 1914 — known only from the type locality in SW Kenya.
Figures 25-26 in On the jumping spider Erica eugenia Peckham & Peckham 1892 (Araneae: Salticidae: Simonellini) from Brazil
Figures 25-26. Habitat of record for Erica eugenia in the Brazilian Cerrado, sensu strictu.
Figures 15–16 in On the jumping spider Erica eugenia Peckham & Peckham 1892 (Araneae: Salticidae: Simonellini) from Brazil
Figures 15–16. Epigynum of Erica eugenia from the Brazilian Cerrado. 15, Ventral view.
Figures 13–14 in On the jumping spider Erica eugenia Peckham & Peckham 1892 (Araneae: Salticidae: Simonellini) from Brazil
Figures 13–14. Epigynum of Erica eugenia from the Brazilian Cerrado. 13, Ventral view.
Figures 1–4 in On the jumping spider Erica eugenia Peckham & Peckham 1892 (Araneae: Salticidae: Simonellini) from Brazil
Figures 1–4. Habitus of Erica eugenia from the Brazilian Cerrado. 1, Female, lateral view. 2, Male,
Figures 11–12 in On the jumping spider Erica eugenia Peckham & Peckham 1892 (Araneae: Salticidae: Simonellini) from Brazil
Figures 11–12. Posterior view, left chelicera of Erica eugenia from the Brazilian Cerrado.
FIGURE 7 in Larval development of the crab Amphithrax hemphilli (Rathbun, 1892) (Decapoda, Brachyura, Mithracidae) described from laboratory-reared material
FIGURE 7. Cladogram of species of Mithrax and allies for the megalopa stage, with phylogeny constructed from Windsor & Felder (2014) and Assugeni et al. (2017). Characteristics: (1) setae on the peduncle of the antennule; (2) aesthetascs on the exopod of the antennule; (3) setation of the antenna; (4) setae on the palp of the mandible; (5) setae on the coxal endite of the maxillule; (6) setae on the basial endite of the maxillule; (7) setae on the endopod of the maxillule; (8) setae on the epidod of the maxillule; (9) setae on the coxal endite of the maxilla; (10) setae on the basial endite of the maxilla; (11) setae on the endopod of the maxilla; (12) setae on the scaphognathite of the maxilla; (13) setae on the basis of the first maxilliped; (14) setae on the endopod of the first maxilliped; (15) setae on the exopod of the first maxilliped; (16) setae on the endopod of the second maxilliped; (17) setae on the exopod of the second maxilliped; (18) setae on the coxa of the third maxilliped; (19) setae on the basischium of the third maxilliped; (20) setae on the endopod of the third maxilliped; (21) setae on the exopod of the third maxilliped, and (22) setae on the pleon. Different colors indicate differences among species; equal colors indicate similarity.
FIGURE 4 in Larval development of the crab Amphithrax hemphilli (Rathbun, 1892) (Decapoda, Brachyura, Mithracidae) described from laboratory-reared material
FIGURE 4. Amphithrax hemphilli (Rathbun, 1892), megalopa stage. (A) maxilliped I; (B) maxilliped II; (C) maxilliped III; (D) pleopods 1–4 and uropod; (E) pereiopods 1–5; (F) dorsal and lateral view of pleon and telson. Scale bars: A–C: 0.1 mm; D–F: 0.2 mm.
FIGURE 1 in Larval development of the crab Amphithrax hemphilli (Rathbun, 1892) (Decapoda, Brachyura, Mithracidae) described from laboratory-reared material
FIGURE 1. Amphithrax hemphilli (Rathbun, 1892), first zoeal stage. (A) Lateral view; (B) dorsal view; (C) antennule; (D) antenna; (E) mandible; (F) maxillule (G) maxilla; (H) maxilliped I; (I) maxilliped II; (J) maxilliped III; (K) pereiopods; (L) dorsal view of pleon and telson. Scale bars: A, B, L: 0.2 mm; C–K: 0.1 mm.
FIGURE 6 in Larval development of the crab Amphithrax hemphilli (Rathbun, 1892) (Decapoda, Brachyura, Mithracidae) described from laboratory-reared material
FIGURE 6. Cladogram of species of Mithrax and allies for the second zoeal stage, with phylogeny constructed from Windsor & Felder (2014) and Assugeni et al. (2017). Characteristics: (1) setae on the anterodorsal region of the carapace; (2) setae on the posterodorsal region of the carapace; (3) setae on the ventral margin of the carapace; (4) aesthetascs on the antennule; (5) setae on the antennule; (6) setae on the coxal endite of the maxillule; (7) setae on the basial endite of the maxillule; (8) setae on the endopod of the maxillule; (9) setae on the coxal endite of the maxilla; (10) setae on the basial endite of the maxilla; (11) setae on the endopod of the maxilla; (12) setae on the scaphognathite of the maxilla; (13) setae on the coxa of the first maxilliped; (14) setae on the basis of the first maxilliped; (15) setae on the endopod of the first maxilliped; (16) setae on the coxa of the second maxilliped; (17) setae on the basis of the second maxilliped, and (18) setae on the endopod of the second maxilliped. Different colors indicate differences among species; equal colors indicate similarity.
FIGURE 2 in Larval development of the crab Amphithrax hemphilli (Rathbun, 1892) (Decapoda, Brachyura, Mithracidae) described from laboratory-reared material
FIGURE 2. Amphithrax hemphilli (Rathbun, 1892), second zoeal stage. (A) Lateral view; (B) antennule; (C) antenna; (D) mandible; (E) maxillule (F) maxilla; (G) maxilliped I; (H) maxilliped II; (I) maxilliped III; (J) pereiopods; (K) dorsal view of pleon and telson. Scale bars: A, J, K: 0.2 mm; B–I: 0.1 mm.
FIGURE 5 in Larval development of the crab Amphithrax hemphilli (Rathbun, 1892) (Decapoda, Brachyura, Mithracidae) described from laboratory-reared material
FIGURE 5. Cladogram of species of Mithrax and allies for the first zoeal stage, with phylogeny constructed from Windsor & Felder (2014) and Assugeni et al. (2017). Characteristics: (1) setae on the anterodorsal region of the carapace; (2) setae on the posterodorsal region of the carapace; (3) setae on the ventral margin of the carapace; (4) aesthetascs on the antennule; (5) setae on the antennule; (6) setae on the coxal endite of the maxillule; (7) setae on the basial endite of the maxillule; (8) setae on the endopod of the maxillule; (9) setae on the coxal endite of the maxilla; (10) setae on the basial endite of the maxilla; (11) setae on the endopod of the maxilla; (12) setae on the scaphognathite of the maxilla; (13) setae on the coxa of the first maxilliped; (14) setae on the basis of the first maxilliped; (15) setae on the endopod of the first maxilliped; (16) setae on the coxa of the second maxilliped; (17) setae on the basis of the second maxilliped, and (18) setae on the endopod of the second maxilliped. Different colors indicate differences among species; equal colors indicate similarity.
FIGURES 24–28 in Two new species of cave-dwelling Charinus Simon, 1892 from Brazil (Arachnida: Amblypygi: Charinidae)
FIGURES 24–28. Charinus spelaeus sp. n.: Female paratype (ISLA 12789): 24. Gonopod. Male paratype (ISLA 12790): 25. Ventral view of the gonopod. 26. Dorsal view of the gonopod. Charinus santanensis sp. n.: Male paratype (ISLA 12778): 27. Ventral view of the gonopod. 28. Dorsal view of the gonopod. Structures indicated: GO = genital operculum, Fi = fistula (gonopod tube), Pi = processus internus, LaM = lamina medialis, LoL1 = lobus lateralis primus, LoL2 = lobus lateralis secundus, LoD = lobus dorsalis.
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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)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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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.