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285 results for “transition zone”
FIGURE 12 in Four new species of anthuroids (Peracarida: Isopoda) from the temperate-tropical transition zone of the western coast of Baja California Peninsula, Mexico
FIGURE 12. Colanthura guerreronegroensis sp. nov., holotype, female, 8.7 mm, CIB-0069_ISO 16, Guerrero Negro Lagoon, Baja California Peninsula, Mexico, station 4. A) Pereopod 1; B) pereopod 2; C) pereopod 3; D) pereopod 4; E) pereopod 5; F) pereopod 6.
FIGURE 5 in Four new species of anthuroids (Peracarida: Isopoda) from the temperate-tropical transition zone of the western coast of Baja California Peninsula, Mexico
FIGURE 5. Cortezura lluchbeldai sp. nov., holotype, female, 9.8 mm, CIB-0058_ISO 5, Guerrero Negro Lagoon, Baja California Peninsula, Mexico, station 9. A) Body, dorsal view; B) detail of telson; C) antennula; D) antenna; E) mandible; F) maxilla; G) maxilliped.
FIGURE 6 in Four new species of anthuroids (Peracarida: Isopoda) from the temperate-tropical transition zone of the western coast of Baja California Peninsula, Mexico
FIGURE 6. Cortezura lluchbeldai sp. nov., holotype, female, 9.8 mm, CIB-0058_ISO 5, Guerrero Negro Lagoon, Baja California Peninsula, Mexico, station 9. A) pereopod 1; B) palm of pereopod 1; C) pereopod 2; D) pereopod 3; E) pereopod 4; F) pereopod 5.
FIGURE 4 in Four new species of anthuroids (Peracarida: Isopoda) from the temperate-tropical transition zone of the western coast of Baja California Peninsula, Mexico
FIGURE 4. Amakusanthura lucinae sp. nov., holotype, female, 8 mm, CIB-0055_ISO 2, Guerrero Negro Lagoon, Baja California Peninsula, Mexico, station 5. A) Pereopod 6; B) pereopod 7; C) pleopod 1; D) pleopod 2; E) uropodal endopod; F) uropodal exopod.
Dataset for paper "Southward shift and intensification of the intertropical convergence zone in the North Pacific across the mid-Pleistocene transition" submittted to Geophysical Research Letters
<p>Data of SST and SSS from <i>G. ruber</i> 𝛿18O and Mg/Ca of core ODP871 (5°33′N, 172°21′E, water depth 1255 m) in the central equatorial Pacific.</p>
Dataset for "Ferric-iron-bearing silicates at the base of the mantle transition zone"
<p>Single crystal X-ray diffraction raw data supporting the results of the manuscript.</p><p>Powder X-ray diffraction raw data supporting the results of the manuscript.</p><p>Powder X-ray diffraction processed data supporting the results of the manuscript.</p><p>Submitted to Journal of Geophysical Research: Solid Earth.</p>
Reef fish assemblage through space and time in a thermal transition zone in the southwestern Atlantic
Open the record for dataset details and reuse information.
Data for 'Tomography of upper mantle and transition zone in Southeast Asia'
<p>Two checkerboard results, a synthetic test and a ISC-EHB tomography result using AST method. See the readme.txt file for details.</p>
Subspecies and Distribution. E.z.zebraLinnaeus,1758—SSouthAfrica(S&WedgeofthecentralplateauintheEasternandWesternCapeProvinces). E. z. hartmannae Matschie, 1898 — W Namibia (mountainous transition zone between the Namib Desert and the Namibian central plateau); possibly in SW Angola. in Equidae
Subspecies and Distribution. E.z.zebraLinnaeus,1758—SSouthAfrica(S&WedgeofthecentralplateauintheEasternandWesternCapeProvinces). E. z. hartmannae Matschie, 1898 — W Namibia (mountainous transition zone between the Namib Desert and the Namibian central plateau); possibly in SW Angola.
Subspecies and Distribution. T.n.napuF.Cuvier,1822—SMyanmar,Thai/MalayPeninsula,islandsoffWMalayPeninsula(Langkawi&Pangkor),Borneo,SSumatra,BangkaI,islandsoffBorneo(Laut&Serasan). T.n.bangue:Chasen&Kloss,1931—BanggiIandBalembanganI,offNBorneo. T.n.bunguranensisMiller,1901—NatunaIs(=Bunguran),oftWBorneo. T.n.neubronneriSody,1931—NSumatra. T.n.nmiasisLyon,1916—NiasI,offWSumatra. T.n.rufulusMiller,1900—TiomanI,offEMalayPeninsula,RiauandLinggaArchipelagos. T. n. terutus Thomas & Wroughton, 1909 — Terutau I, off W Malay Peninsula. The species was recently reconfirmed for Singapore. Maps that include Vietnam, Cambodia, and Laos in the distribution range are based on the earlier assumption that 7. versicolor was a subspecies of 1. napu. Subsequent studies have indicated that 7. versicolor is a distinct species, and that the range of 1. napu therefore does not extend into Cambodia, Laos, and Vietnam. The northern limit on the Thai-Malay peninsula is not well defined. Specimens of 1. napu have been collected from as far north as Bankachon in southern Myanmar (10° 08" N), but despite fairly intensive camera-trapping in Kui Buri National Park, Thailand (12° N), 7. napu has not been photographed there. At the northern margin ofits range, it is generally rare. It has been reported, for example, that during the flooding of the Chiew Larn Reservoir (Surat Thani Province; about 9° N, 98° 45' E), only six 7. napu were rescued compared with 172 71. kanchil. This area is the transition zone from wetter evergreen forest to drier deciduous types, and it might be that 7° napu is not well adapted to the drier forest types towards the northern limit ofits range. There are unconfirmed reports of the species on Java, where it may have been confused with one of the two color morphs of 7. javanicus. As explained in the Taxonomy section, the subspecific status of the populations of several islands remains unclear. in Tragulidae
Subspecies and Distribution. T.n.napuF.Cuvier,1822—SMyanmar,Thai/MalayPeninsula,islandsoffWMalayPeninsula(Langkawi&Pangkor),Borneo,SSumatra,BangkaI,islandsoffBorneo(Laut&Serasan). T.n.bangue:Chasen&Kloss,1931—BanggiIandBalembanganI,offNBorneo. T.n.bunguranensisMiller,1901—NatunaIs(=Bunguran),oftWBorneo. T.n.neubronneriSody,1931—NSumatra. T.n.nmiasisLyon,1916—NiasI,offWSumatra. T.n.rufulusMiller,1900—TiomanI,offEMalayPeninsula,RiauandLinggaArchipelagos. T. n. terutus Thomas & Wroughton, 1909 — Terutau I, off W Malay Peninsula. The species was recently reconfirmed for Singapore. Maps that include Vietnam, Cambodia, and Laos in the distribution range are based on the earlier assumption that 7. versicolor was a subspecies of 1. napu. Subsequent studies have indicated that 7. versicolor is a distinct species, and that the range of 1. napu therefore does not extend into Cambodia, Laos, and Vietnam. The northern limit on the Thai-Malay peninsula is not well defined. Specimens of 1. napu have been collected from as far north as Bankachon in southern Myanmar (10° 08" N), but despite fairly intensive camera-trapping in Kui Buri National Park, Thailand (12° N), 7. napu has not been photographed there. At the northern margin ofits range, it is generally rare. It has been reported, for example, that during the flooding of the Chiew Larn Reservoir (Surat Thani Province; about 9° N, 98° 45' E), only six 7. napu were rescued compared with 172 71. kanchil. This area is the transition zone from wetter evergreen forest to drier deciduous types, and it might be that 7° napu is not well adapted to the drier forest types towards the northern limit ofits range. There are unconfirmed reports of the species on Java, where it may have been confused with one of the two color morphs of 7. javanicus. As explained in the Taxonomy section, the subspecific status of the populations of several islands remains unclear.
Subspecies and Distribution. D. m. merriami Mearns, 1890 — SW USA and NW Mexico (desert regions from N Nevada and extreme SW Utah, through SE California and SW Arizona, to NE Baja California and Sonora). D. m. ambiguus Merriam, 1890 — SW USA and NW Mexico (N portion of the Chihuahuan Desert from NC New Mexico and W Texas, through E Chihuahua and Coahuila, to NE Durango, N Zacatecas, and C Nuevo Leon). D. m. annulus Huey, 1951 — NW Mexico (coastal plains of the Gulf of California, SE Baja California). D. m. arenivagus Elliot, 1904 — SW USA and NW Mexico (S Mojave Desert of SC California and E of Sierra Juarez and Sierra San Pedro Martir to C Baja California). D. m. atronasus Merriam, 1894 — NC Mexico (southern portion of the Chihuahuan Desert from EC Zacatecas, SE Coahuila, and SW Nuevo Leon to Aguascalientes and San Luis Potosi). D. m. brunensis Huey, 1951 — NW Mexico (Gulf of California coast of NE Baja California Sur). D. m. collinus Lidicker, 1960 — SW USA (San Felipe, Earthquake, La Puerta, and Aguanga valleys of SW California). D. m. frenatus Bole, 1936 — SW USA (SW Utah and NW Arizona). D. m. insularis Merriam, 1907 — NW Mexico (San José I, Gulf of California, Baja California Sur). D. m. margaritae Merriam, 1907 — NW Mexico (Santa Margarita I, Baja California Sur). D. m. mayensis Goldman, 1928 — NW Mexico (Gulf of California coastal plains of S Sonora and N Sinaloa). D. m. melanurus Merriam, 1893 — NW Mexico (Magdalena Plains and Cape Region of S Baja California Sur). D. m. mitchelli Mearns, 1897 — NW Mexico (Tiburon I, Gulf of California, Sonora). D. m. olivaceus Swarth, 1929 — SW USA and NW Mexico (transitional zone between the Sonoran Desert of SE Arizona and NE Sonora, and the Chihuahuan Desert of SW New Mexico and NW Chihuahua). D. m. parvus Rhoads, 1894 — SW USA (San Bernardino and San Jacinto valleys of SW California). D. m. platycephalus Merriam, 1907 — NW Mexico (Pacific slope S of the Sierra San Pedro Martir, S Baja California to the Vizcaino Desert of N Baja California Sur). D. m. quintinensis Huey, 1951 — NW Mexico (San Quintin Plain, Pacific coast of NW Baja California). D. m. trinidadensis Huey, 1951 — SW USA and NW Mexico (S California and N Baja California). D. m. vulcani Benson, 1934 — SW USA (disjunct and restricted distribution in Toroweap Valley, NW Arizona). in Heteromyidae
Subspecies and Distribution. D. m. merriami Mearns, 1890 — SW USA and NW Mexico (desert regions from N Nevada and extreme SW Utah, through SE California and SW Arizona, to NE Baja California and Sonora). D. m. ambiguus Merriam, 1890 — SW USA and NW Mexico (N portion of the Chihuahuan Desert from NC New Mexico and W Texas, through E Chihuahua and Coahuila, to NE Durango, N Zacatecas, and C Nuevo Leon). D. m. annulus Huey, 1951 — NW Mexico (coastal plains of the Gulf of California, SE Baja California). D. m. arenivagus Elliot, 1904 — SW USA and NW Mexico (S Mojave Desert of SC California and E of Sierra Juarez and Sierra San Pedro Martir to C Baja California). D. m. atronasus Merriam, 1894 — NC Mexico (southern portion of the Chihuahuan Desert from EC Zacatecas, SE Coahuila, and SW Nuevo Leon to Aguascalientes and San Luis Potosi). D. m. brunensis Huey, 1951 — NW Mexico (Gulf of California coast of NE Baja California Sur). D. m. collinus Lidicker, 1960 — SW USA (San Felipe, Earthquake, La Puerta, and Aguanga valleys of SW California). D. m. frenatus Bole, 1936 — SW USA (SW Utah and NW Arizona). D. m. insularis Merriam, 1907 — NW Mexico (San José I, Gulf of California, Baja California Sur). D. m. margaritae Merriam, 1907 — NW Mexico (Santa Margarita I, Baja California Sur). D. m. mayensis Goldman, 1928 — NW Mexico (Gulf of California coastal plains of S Sonora and N Sinaloa). D. m. melanurus Merriam, 1893 — NW Mexico (Magdalena Plains and Cape Region of S Baja California Sur). D. m. mitchelli Mearns, 1897 — NW Mexico (Tiburon I, Gulf of California, Sonora). D. m. olivaceus Swarth, 1929 — SW USA and NW Mexico (transitional zone between the Sonoran Desert of SE Arizona and NE Sonora, and the Chihuahuan Desert of SW New Mexico and NW Chihuahua). D. m. parvus Rhoads, 1894 — SW USA (San Bernardino and San Jacinto valleys of SW California). D. m. platycephalus Merriam, 1907 — NW Mexico (Pacific slope S of the Sierra San Pedro Martir, S Baja California to the Vizcaino Desert of N Baja California Sur). D. m. quintinensis Huey, 1951 — NW Mexico (San Quintin Plain, Pacific coast of NW Baja California). D. m. trinidadensis Huey, 1951 — SW USA and NW Mexico (S California and N Baja California). D. m. vulcani Benson, 1934 — SW USA (disjunct and restricted distribution in Toroweap Valley, NW Arizona).
Figure 7 in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 7. Live coloration of the three species of Diogenes: A–C, left cheliped, outer aspect; D–F, cephalothorax and cephalic appendages; G–I, detailed photographs of the inner face of palms, showing the shape of the row of tubercles; J–L, left pereiopod 2. A, D, G, J, Diogenes pugilator; B, E, H, K, Diogenes armatus sp. nov. C, F, I, L, Diogenes curvimanus.
Figure 6 in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 6. Diogenes curvimanus. ♂ 2.6 mm, Guadalquivir N.P., Huelva, Spain, neotype, (MNHN-IU-2019-3214): A, left cheliped, outer aspect; B, left cheliped, dorsal aspect; D, left pereiopod 2 (insets: variations in P3 carpus; dactylus inner aspect); E, left pereiopod 4, outer aspect; F, telson, dorsal aspect; G, merus, mesial view (setae omitted). Diogenes curvimanus. ♀ 2.9 mm, Ría de Arousa, Galicia, Spain (ZSMA2019 0399): C, Left cheliped, outer aspect (arrow indicating bispinose protuberance). (Scales: A–B, G = 1 mm; C, E–F = 0.5 mm; D = 2.0 mm).
Figure 3 in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 3. Diogenes armatus sp. nov. ♂ 3.4 mm, Torregorda, Cádiz, Spain, holotype, (MNHN-IU-2019-3213): A, anterior part of body; B, right antennule, inner aspect; C, ophtalmic scales; D, left maxiliped 3 (inset: detail of the spines, ventral aspect); E, right cheliped, dorsal aspect; F, left pereiopod 2 (insets: variations in P3 carpus; dactylus inner aspect); G, telson, dorsal view. (Scales: A, E–G = 1 mm, B–D = 0.5 mm).
Figure 4 in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 4. Diogenes armatus sp. nov. ♂ 3.4 mm, Torregorda, Cádiz, Spain, holotype, (MNHN-IU-2019-3213): A, male left cheliped, outer aspect (arrow indicating bispinose protuberance); B, left cheliped, dorsal aspect; C, left cheliped inner surface; D, left cheliped dactylus, dorsal aspect; F, left pereiopod 4, outer aspect; G, left cheliped merus, mesial view (setae omitted). Diogenes armatus sp. nov. ♀ 3.8 mm, Isla Canela, Huelva, Spain, allotype, (MNHN-IU-2014-5736): E, female left cheliped, outer aspect. (Scales: A, C, G = 2 mm; B, D, E = 1 mm; F = 0.5 mm).
Figure 5 in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 5. Diogenes curvimanus. ♂ 2.6 mm, Guadalquivir N.P., Huelva, Spain, neotype, (MNHN-IU-2019-3214): A, anterior part of body; B, right antennular, inner aspect; C, ophtalmic scales; D, maxiliped 3 (inset: detail of the spines, ventral aspect); E, right cheliped, outer aspect. (Scales: A = 1 mm, B = 0.2 mm, C–E = 0.5 mm).
Figure 2. Diogenes pugilator s.s in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 2. Diogenes pugilator s.s. ♂ 3.0 mm, Frontignan, France, neotype, (MNHN-IU-2019-3215): A, left cheliped, outer aspect (arrow indicating bispinose protuberance); B, left cheliped, dorsal aspect (inset: detail of the row of tubercles on the lower, inner surface). Diogenes pugilator s.s. ♀ 2.5 mm, La Carihuela, Málaga, Spain, topotype, (IEOCD-BR/2660-2661): C, left cheliped, outer aspect. Diogenes pugilator s.s. ♂ 2.7 mm Frontignan, France, topotype, (ZSMA2019 0400): D, left pereiopod 2 (insets: variations in P3 carpus; dactylus inner aspect); E, pereiopod 4; F, merus, mesial view (setae omitted). (Scales: A–C, F = 2 mm, D = 1 mm, E = 0.5 mm).
Figure 1. Diogenes pugilator s.s in Redescription of the hermit crab Diogenes pugilator (Decapoda: Anomura) reveals the existence of a species complex in the Atlanto-Mediterranean transition zone, resulting in the resurrection of D. curvimanus and the description of a new species
Figure 1. Diogenes pugilator s.s. ♂ 3.0 mm, Frontignan, France, neotype, (MNHN-IU-2019-3215): A, anterior part of body; B, ophtalmic scales; E, right cheliped, outer aspect; F, telson, dorsal aspect. Diogenes pugilator s.s. ♂ 2.7 mm, Frontignan, France, topotype (ZSMA2019 0400): C, right antennular, inner view; D, left maxiliped 3, (inset: detail of the spines, ventral aspect). (Scales: A, C, E = 1 mm, B, D, F = 0.5 mm).
FIGURE 2 in Species distribution ranges of Ilyocryptus Sars, 1862 (Cladocera: Ilyocryptidae) fit the transitional zone between Boreal and Tropical Provinces in the Far East
FIGURE 2. Ilyocryptus yooni Jeong et al., 2012, an adult parthenogenetic female from a large pond in Ho Chi Minh City, South Vietnam: A, general view. B, setae at posterior valve margin. C, postabdomen. D, Its preanal portion. E, Distal portion of postabdomen. F, Antenna I. Scale bars: 0.1 mm.
FIGURE 1 in Species distribution ranges of Ilyocryptus Sars, 1862 (Cladocera: Ilyocryptidae) fit the transitional zone between Boreal and Tropical Provinces in the Far East
FIGURE 1.Original records of Ilyocryptus present in southern and northern territories of the Pacific Region only (A), and penetrating the transitional zone between Boreal ("Palaeactic") and Oriental Provinces (B). Abbreviations: WE—species widely distributed in North Eurasia; ST—southern tropical species; EN—Far Eastern endemics.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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OpenNeuro
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