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3,101 results for “Historical”

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Fig. 2 in Journey to the West: Trans-Pacific Historical Biogeography of Fringehead Blennies in the Genus (Teleostei: Blenniiformes).

Fig. 2. Individual gene trees of the Neocliniini and its outgroup, Alloclinus holderi, implemented under Maximum likelihood analysis in RAxML: (a) COI, (b) cytochrome b, (c) 12S + 16S, (d) TMO-4C4, (e) RAG-1.

opencc-by-4.0Apr 2020View details →
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Fig. 1 in Journey to the West: Trans-Pacific Historical Biogeography of Fringehead Blennies in the Genus (Teleostei: Blenniiformes).

Fig. 1. Representatives of fringehead blennies included in this study. (a) Neoclinus okazakii, (b) N. stephensae, (c) N. bryope, (d) N. uninotatus, (e) N. nudus, (f) N. blanchardi. A, C, E are western Pacific species, while B, D, F are eastern Pacific species. Photos by W. Hongjamrassilp.

opencc-by-4.0Apr 2020View details →
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Fig. 3 in Journey to the West: Trans-Pacific Historical Biogeography of Fringehead Blennies in the Genus (Teleostei: Blenniiformes).

Fig. 3. Species tree for the Neocliniini from concatenated six genetic markers dataset analyzed using Maximum Parsimony (MP), Maximum Likelihood (ML), and Bayesian Inference (BI). Numbers on each node of the tree from left to right are: posterior probability from BI, bootstrap value from ML, and bootstrap value from MP. Asterisk means no support value was shown in the result.

opencc-by-4.0Apr 2020View details →
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Fig. 7 in New earthworm species from NIBR's Jeju-do biosphere compared to historical and new Japanese types (Oligochaeta: Megadrilacea: Megascolecidae)

Fig. 7. Amynthas tralfamadore sp. nov. holotype from NIBR Korea; [boxed is a X2 enlargement of 9 lhs spermatheca and 18 rhs male pore].

opencc-by-4.0Aug 2012View details →
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Fig. 6. A in New earthworm species from NIBR's Jeju-do biosphere compared to historical and new Japanese types (Oligochaeta: Megadrilacea: Megascolecidae)

Fig. 6. A. micronarius Japanese Watarase specimen-lhs; Nogeyama specimen-middle; Incheon's NIBR (INV0000246442) Jeju-conservatory specimen [boxed X2 enlargement of spermathecal and male pores in 5/6 rhs & 18 rhs]-rhs.

opencc-by-4.0Aug 2012View details →
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Fig. 3 in New earthworm species from NIBR's Jeju-do biosphere compared to historical and new Japanese types (Oligochaeta: Megadrilacea: Megascolecidae)

Fig. 3. Amynthas parvicystis after original (Goto & Hatai, 1899: fig. 8)-possibly a composite for different species and with segments 7 & 8 miscounted?

opencc-by-4.0Aug 2012View details →
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Fig. 5 in Historical biogeography highlights the role of Miocene landscape changes on the diversification of a clade of Amazonian tree frogs

Fig. 5 Dorsolateral views of Osteocephalus. a O. leprieurii sensu stricto, Kaw mountain, French Guiana. b O. leprieurii, AF1824, Mana, French Guiana. c O. yasuni sensu stricto, QCAZ69010, Estación Cientí- fica Yasuní, Orellana, Ecuador. d O. yasuni, QCAZ55994, Lorocachi, Pastaza, Ecuador. e O. deridens, QCAZ56031, Lorocachi, Pastaza, Ecuador. f O. fuscifacies, QCAZ59887, Parque Nacional Llanganates, Pastaza, Ecuador. g O. aff. leoniae 2, AF4513 (sequenced), San Martín, Peru. h O. planiceps, QCAZ55881, Lorocachi, Pastaza, Ecuador. Photographs: a–b, g by Antoine Fouquet; c–f, h by Santiago Ron (BIOWEB, Licence: CC BY-NC-ND 4.0)

opencc-by-4.0Nov 2022View details →
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Fig. 4 in Historical biogeography highlights the role of Miocene landscape changes on the diversification of a clade of Amazonian tree frogs

Fig. 4 Dorsolateral and ventral views of Osteocephalus. a O. cabrerai, CORBIDI120, Tara- poa, Sucumbíos, Ecuador. b O. helenae, AF2427 (sequenced), Nassau, Suriname. c O. helenae, Amapá, Brazil. d O. helenae, Voltaire, French Guiana. e–f O. aff. helenae 2 'morph cabrerai', AF2357 (sequenced), Mapaou, French Guiana. g O. aff. helenae 2 'morph cabrerai', AF3358 (sequenced), Bakhuis, Surinam. h O. aff. helenae 2 'morph cabrerai', St. Georges, French Guiana. Photographs: a by Pablo Venegas (BIOWEB, Licence: CC BY-NC-ND 4.0); b–h by Antoine Fouquet

opencc-by-4.0Nov 2022View details →
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Fig. 3 in Historical biogeography highlights the role of Miocene landscape changes on the diversification of a clade of Amazonian tree frogs

Fig. 3 Dorsolateral views of Osteocephalus. a O. alboguttatus sensu stricto, QCAZ15972, Puyo-Canelos Road, Pastaza, Ecuador. b O. mimeticus sensu stricto, AF4442 (sequenced), San José, San Martín, Peru. c O. buckleyi sensu stricto, Canelos, Pastaza, Ecuador. d O. vilmae, QCAZ51205, Pompeya-Iro Road km 80, Orellana, Ecuador. e O. mutabor, QCAZ56066, Lorocachi, Pastaza, Ecuador. f O. mutabor, QCAZ39588, Río Pucayacu, Pastaza, Ecuador. g O. taurinus sensu stricto, Reserva Ducke, Amazonas, Brazil. h O. oophagus sensu stricto, Reserva Ducke, Amazonas, Brazil. Photographs: a, d–f by Santiago Ron (BIOWEB, Licence: CC BY-NC-ND 4.0); b by Antoine Fouquet; c, g–h by Diego Ortiz

opencc-by-4.0Nov 2022View details →
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Fig. 3 in Reconstructed historical distribution and phylogeography unravels non-steppic origin of Caucasotachea vindobonensis (Gastropoda: Helicidae)

Fig. 3 Reconstruction of the geographic range evolution. For the geographic position of the samples and the subdivision of the range, see Fig. 1. The ultrametric ML tree shows phylogenetic relationships of the Caucasotachea vindobonensis haplotypes based on COI sequences. High branch supports for the main clades are indicated by black/gray dots (gray aLRT >0.80; black aLRT>0.95). The colored symbols at the tips indicate the current geographic origin of the haplotypes (see also Supplementary Table 1). Values at the branches indicate all alternative scenarios with likelihoods above 10% for the origin of the clades' common ancestors (BK Balkans, CP Carpatho-Pannon, PC northwestern, NW Ponto-Caspian). The ancestors were allowed to occupy a maximum of three geographic areas. Migration was permitted between all regions, but lower probability (B0.25^ instead of B1.0^) was assigned in the dispersal constraints for migration between areas not being immediately adjacent (between north-western and the Balkans)

opencc-by-4.0Jul 2017View details →
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Fig. 2 in Reconstructed historical distribution and phylogeography unravels non-steppic origin of Caucasotachea vindobonensis (Gastropoda: Helicidae)

Fig. 2 Median-joining networks of Caucasotachea vindobonensis COI haplotypes with assignment to the defined regions of species distribution

opencc-by-4.0Jul 2017View details →
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Fig. 1 in Reconstructed historical distribution and phylogeography unravels non-steppic origin of Caucasotachea vindobonensis (Gastropoda: Helicidae)

Fig. 1 Range of the Caucasotachea vindobonensis with localization of sampling sites and defined regions of species distribution used for genetic analyses

opencc-by-4.0Jul 2017View details →
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Fig. 4 in Reconstructed historical distribution and phylogeography unravels non-steppic origin of Caucasotachea vindobonensis (Gastropoda: Helicidae)

Fig. 4 Potential distribution of Caucasotachea vindobonensis during the LGM based on different climate models (CCSM4, MIROC-ESM). Warmer/darker colors indicate more suitable climatic conditions

opencc-by-4.0Jul 2017View details →
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species according to Broadley (1994). These may well be the result of continuing confusion over the placement of Keta. Given the localities known from Lunda Norte, it seems likely that the species occurs in other northern regions of Angola. MAP 363. Distribution of Scaphiophis albopunctatus in Angola. in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)

species according to Broadley (1994). These may well be the result of continuing confusion over the placement of Keta. Given the localities known from Lunda Norte, it seems likely that the species occurs in other northern regions of Angola. MAP 363. Distribution of Scaphiophis albopunctatus in Angola.

opencc-by-4.0Sep 2018View details →
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Telescopus finkeldeyi Haacke, 2013 DAMARA TIGER SNAKE Telescopus finkeldeyi Haacke 2013:281. Holotype: TM 53542 (collector J.A. van Rooyen). Type locality: "Rössing Uranium mine area, Swako- mund [sic] district (2214Db) Namibia." Global conservation status (IUCN): Not Evaluated. Global distribution: The species is known from Angola and Namibia. Ocurrences in Angola (Map 364): The species occurs in southwestern Angola. Namibe: "5 km north Namibé" [-15.20000, 12.15000] (Haacke 2013:285). Taxonomic and distributional notes: Some earlier records of T. semiannulatus polystictus in Namibia actually refer to this recently described species. MAP 364. Distribution of Telescopus finkeldeyi in Angola. in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)

Telescopus finkeldeyi Haacke, 2013 DAMARA TIGER SNAKE Telescopus finkeldeyi Haacke 2013:281. Holotype: TM 53542 (collector J.A. van Rooyen). Type locality: "Rössing Uranium mine area, Swako- mund [sic] district (2214Db) Namibia." Global conservation status (IUCN): Not Evaluated. Global distribution: The species is known from Angola and Namibia. Ocurrences in Angola (Map 364): The species occurs in southwestern Angola. Namibe: "5 km north Namibé" [-15.20000, 12.15000] (Haacke 2013:285). Taxonomic and distributional notes: Some earlier records of T. semiannulatus polystictus in Namibia actually refer to this recently described species. MAP 364. Distribution of Telescopus finkeldeyi in Angola.

opencc-by-4.0Sep 2018View details →
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with Hemidactylus brookii angulatus Hallowell, 1852. The species was recently recorded from Quiçama National Park in Luanda Province (M. Marques, L. Ceríaco, A. Bauer and D. Blackburn pers. obs. 2015, 2016). MAP 130. Distribution of Hemidactylus bayonii in Angola. in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)

with Hemidactylus brookii angulatus Hallowell, 1852. The species was recently recorded from Quiçama National Park in Luanda Province (M. Marques, L. Ceríaco, A. Bauer and D. Blackburn pers. obs. 2015, 2016). MAP 130. Distribution of Hemidactylus bayonii in Angola.

opencc-by-4.0Sep 2018View details →
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ly a misidentification as today the recognized distribution of this species is restricted to western Africa. It is possible that the Cabinda frog may be referable to Phrynobatrachus auritus Boulenger, 1900. MAP 96. Distribution of Phrynobatrachus plicatus in Angola. in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)

ly a misidentification as today the recognized distribution of this species is restricted to western Africa. It is possible that the Cabinda frog may be referable to Phrynobatrachus auritus Boulenger, 1900. MAP 96. Distribution of Phrynobatrachus plicatus in Angola.

opencc-by-4.0Sep 2018View details →
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suggests that northern specimens of R. barnardi should be reexamined to confirm their specific identity. MAP 154. Distribution of Rhoptropus sp. in Angola. in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)

suggests that northern specimens of R. barnardi should be reexamined to confirm their specific identity. MAP 154. Distribution of Rhoptropus sp. in Angola.

opencc-by-4.0Sep 2018View details →
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1987 in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)

1987:179; Schiøtz 1975:61, 1999:247; Channing 2001:188). Cuando Cubango: "Cubango basin (6b)" [-14.67458, 17.73544] (Conradie et al. 2016:8-9, 15). Taxonomic and distributional notes: The type locality was for some time the only known record for K. kuvangensis. Recently, Conradie et al. (2016) cited the species from Cuando Cubango region. Other authors have also identified populations in Zambia as this species (Schiøtz 1999; Channing 2001). MAP 59. Distribution of Kassina kuvangensis in Angola.

opencc-by-4.0Sep 2018View details →
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FIGURE 29 in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)

FIGURE 29. Map with localities where endemic species occur in Angola. Orange stars represent localities where endemic reptile species occur, green starts represent localities where amphibian endemics occur, red starts represent localities where both amphibian and reptile endemics have been recorded.

opencc-by-4.0Sep 2018View details →

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neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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dandi-nwb
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Last verified 2026-04-30Open record

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.

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behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
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Last verified 2026-04-29Open record

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