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163 results for “southern Peru”
FIGURE 3 in An endemic new species of Ameiva (Squamata: Teiidae) from an isolated dry forest in southern Peru
FIGURE 3. Coloration and pattern of adult male paratypes of Ameiva reticulata sp. nov. in preservative: (A) Dorsal and (B) lateral views of CORBIDI 9917, (C) dorsal and (D) lateral views of CORBIDI 10086, and (E) dorsal and (F) lateral views of CORBIDI 10084. Photographs by P.J. Venegas.
FIGURE 2 in An endemic new species of Ameiva (Squamata: Teiidae) from an isolated dry forest in southern Peru
FIGURE 2. Holotype of Ameiva reticulata sp. nov. (CORBIDI 8816): dorsal (A), lateral (B) and ventral (C) views of head. Drawings by C. Koch.
FIGURE 4 in A new species of Trachytherus (Notoungulata: Mesotheriidae) from the late Oligocene (Deseadan) of Southern Peru and the middle latitude diversification of early diverging mesotheriids
FIGURE 4. Manual elements of Trachytherus spp. A, Trachytherus ramirezi, right distal ulna and radius (with unfused radial epiphysis), carpals (missing trapezium and pisiform) and proximal metacarpals II–V (MUSM 963); B, right carpals (missing trapezoid and pisiform) and damaged Mc I–V (MUSM 965) of small indeterminate species of Moquegua; C, nearly complete right manus of cf. T. spegazzinianus (MUSM 668); left manus of T. alloxus (UF 91933, reversed to show as right). Abbreviations: cun, cuneiform; ln, lunate; Mc, metacarpal; mg, magnum; pis, pisiform; sc, scaphoid; td, trapezoid; tm, trapezium. Scale bar applies to all.
FIGURE 2 in A new species of Trachytherus (Notoungulata: Mesotheriidae) from the late Oligocene (Deseadan) of Southern Peru and the middle latitude diversification of early diverging mesotheriids
FIGURE 2. Holotype Trachytherus ramirezi sp. nov., MUSM 350. A, right lateral view of cranium and mandible; A', detail of external auditory region of A; B, skull in left lateral view to illustrate the damaged side, revealing the mesodont-to-hypsodont premolars, somewhat hypsodont (rooted) M1, and hypselodont M2–3; C, ventral view of skull and palate; and D, occlusal view of jaw and lower dentitions. Abbreviations: bc, braincase; crm, crista meatus; eam, external auditory meatus; ets, epitypmanic sinus; gf, glenoid fossa; msty, metastyle; pgp, post glenoid process; rtp, retrotympanic process; and smf, suprameatal fossa. Scale bar at D applies to all, except the slightly enlarged A'.
FIGURE 1 in A new species of Trachytherus (Notoungulata: Mesotheriidae) from the late Oligocene (Deseadan) of Southern Peru and the middle latitude diversification of early diverging mesotheriids
FIGURE 1. Map of South America showing the approximate locations of sites that have yielded remains of Oligocene mesotheriids: stars are to indicate locations of undescribed/unclassified Tinguirirican mesotheriid materials; octagons indicate the widely dispersed, Deseadan Trachytherus spegazzinianus; and diamonds indicate localities containing all other recognized species of Trachytherus (Deseadan). The dashed oval circumscribes the area we refer to as the "Bolivian Oroclinal Region," an area that contains all four recognized species of Trachytherus (see text for details). Background map modified from NASA image.
FIGURE 7 in A new species of Trachytherus (Notoungulata: Mesotheriidae) from the late Oligocene (Deseadan) of Southern Peru and the middle latitude diversification of early diverging mesotheriids
FIGURE 7. Phylogeny and historical biogeography of the Mesotheriidae. Cladograms of A and B were based upon the phylogenetic analysis in this study for the early diverging, non-mesotheriine mesotheriids (without the Deltran optimization given fig. 6) combined with the analysis of Croft et al. (2004) for the Mesotheriinae (see also Flynn et al. 2003). That of A includes the "published mesotheriid" (PM) dataset only, whereas B, the "undescribed plus published mesotheriids (U+PM), includes undescribed Tinguirirican material. Question marks indicate the uncertainties of affinities of the Tinguirirican taxa and that of an indeterminate mesotheriine Colhuehuapian (see text). Lines from taxon to map of South America are to indicate the general region(s) from which the taxa are known. The reconstructions of ancestral area presented here are based on the single character coding strategy (see Material and Methods). The bold lines of the cladogram indicate the evolution of the BOR distribution on the tree, whereas thin stems indicate distribution in SSA (see text for comments).
Dataset used in the paper "Contributing to the taxonomic inventory of green colored rain frogs: A new species of the Pristimantis lacrimosus group (Anura, Strabomantidae) from the southern Cordillera Azul, central Peru" by Ernesto Castillo-Urbina, Miguel Vences, César Aguilar-Puntriano, Frank Glaw & Jörn Köhler
Open the record for dataset details and reuse information.
FIGURE 5 in A new genus and species of tanager (Passeriformes, Thraupidae) from the lower Yungas of western Bolivia and southern Peru
FIGURE 5. Spectrograms of vocalizations of Heliothraupis oneilli. The x-axis represents time in seconds, the y-axis represents frequency in kilohertz. All recordings are by DFL unless otherwise noted; "ML #######" refers to the catalog number at Macaulay Library (available at https://macaulaylibrary.org/asset/#######). First, songs from 6 individuals from La Paz, Bolivia, to show variationamong individualswithin apopulation: (A) 22 December 2012. ML 238433. (B) 24 December 2012. ML 238435. (C) 23 December 2012. ML 238434. (D) 24 January 2019. ML 238442. (E) 24 January 2019. ML 238443. (F) 26 January 2019. ML 238446. The following are songs from three different individuals from the Kosñipata road in Cusco, Peru, to show variation at that site: (G) 10 October 2000. Recorded by GHR, ML 258172441. (H) 7 October 2003. ML 238361. (I) 9 June 2004. ML 238417. Finally, examples of the common calls of Heliothraupis oneilli: (J) 24 January 2019. ML 238443. (K) 7 October 2003. ML 238361. (L) 24 January 2019. ML 238442. (M) 26 December 2012. ML 238437.
FIGURE 4 in A new genus and species of tanager (Passeriformes, Thraupidae) from the lower Yungas of western Bolivia and southern Peru
FIGURE 4. Confirmed localities of Heliothraupis oneilli plotted as black dots and predicted distribution based on our modeling, using parameters set at 50% suitability, with the predicted breeding range (in gold) and predicted nonbreeding range (in purple) plotted on a false color map of elevation of the eastern slope of the Andes in western Bolivia and Southern Perú. From the confirmed observations reported, we believe that this species breeds inhigh densities ina small region (~2,500 km2), and then disperses toa much larger zone (~26,000 km2) in the nonbreeding season, resulting in considerablylower population density at thattime.
FIGURE 3 in A new genus and species of tanager (Passeriformes, Thraupidae) from the lower Yungas of western Bolivia and southern Peru
FIGURE 3. Line drawings of external morphological characters of Heliothraupis, based on LSUMZ 195912. (A) Bill structure, (B) outside view of left leg, (C) underside of tail, and (D) dorsal view of open right wing. Drawing by DFL.
Distribution. Cold-temperate waters of the Southern Hemisphere, mainly at 20-60° S except on both coasts of South America, where they occur at most lower latitudes. Concentrated in winter near the coastlines off S Australia, New Zealand, Atlantic coast of South America (Argentina, Brazil), and S Africa (mainly South Africa), but also off Chile, Peru, Tristan da Cunha Is and the E coast of Madagascar; in summer they are found mainly in latitudes of 40-50° S but have been seen in the Antarctic as far as 65° S and around South Georgia Is. in Balaenidae
Distribution. Cold-temperate waters of the Southern Hemisphere, mainly at 20-60° S except on both coasts of South America, where they occur at most lower latitudes. Concentrated in winter near the coastlines off S Australia, New Zealand, Atlantic coast of South America (Argentina, Brazil), and S Africa (mainly South Africa), but also off Chile, Peru, Tristan da Cunha Is and the E coast of Madagascar; in summer they are found mainly in latitudes of 40-50° S but have been seen in the Antarctic as far as 65° S and around South Georgia Is.
Figs 1–5 in Status and revision of the genus Philanglaus Butler, 1882 (Lepidoptera: Cossidae: Hypoptinae) from Southern Peru and Chile
Figs 1–5. Adult specimens of Philanglaus: 1 — P. ornatus (Butler, 1882), ♀, holotype (NHMUK); 2 — P. ornatus, ♂, holotype of Philanglaus penai Clench, 1957, Chile, Pichinahuel, 1100–1400 m, 23–31.I.1954, leg. L.Peña (CMNH); 3 — P. ornatus, ♂, Chile, Caramavida Araulo, 50 m, 13–14.I.1988, leg. J.Gonzales (MWM); 4 — P. xylodopoecila (Zukowsky, 1954) comb.n., ♂, neotype, Peru, Arequipa, 23.III.1936 (MHUB); 5 — P. xylodopoecila, ♂, Chile, Prov. Tarapaca, Tarapaca, 25.I.1992 (MWM). Рис. 1–5. Имаго Philanglaus: 1 —. P. ornatus (Butler, 1882), ♀, голотип (NHMUK); 2 — P. ornatus, ♂, голотип Philanglaus penai Clench, 1957, Chile, Pichinahuel, 1100–1400 m, 23–31.I.1954, leg. L.Peсa (CMNH); 3 — P. ornatus, ♂, Chile, Caramavida Araulo, 50 m, 13–14.I.1988, leg. J.Gonzales (MWM); 4 — P. xylodopoecila (Zukowsky, 1954) comb.n., ♂, неотип, Peru, Arequipa, 23.III.1936 (MHUB); 5 — P. xylodopoecila, ♂, Chile, Prov. Tarapaca, Tarapaca, 25.I.1992 (MWM).
Figs 6–7 in Status and revision of the genus Philanglaus Butler, 1882 (Lepidoptera: Cossidae: Hypoptinae) from Southern Peru and Chile
Figs 6–7. Male genitalia of Philanglaus: 6 — P. ornatus Chile, Caramavida Araulo (Genitalpräparat Heterocera № 28.530) (MWM); 7 — P. xylodopoecila, Chile, Prov. Tarapaca, (Genitalpräparat Heterocera № 28.515) (MWM). Рис. 6–7. Гениталии самцов Philanglaus: 6 — P. ornatus Chile, Caramavida Araulo (Genitalpräparat Heterocera № 28.530) (MWM); 7 —. P. xylodopoecila, Chile, Prov. Tarapaca, (Genitalpräparat Heterocera № 28.515) (MWM).
FIGURE 5 in Arcanumophis, a new genus and generic allocation for Erythrolamprus problematicus (Myers 1986), Xenodontinae (Colubridae) from the Cordillera de Carabaya, southern Peru
FIGURE 5. Autapomorphy of Arcanumophis illustrated by comparing heads of (A) A. problematicus (CORBIDI 18731) and of selected species of Erythrolamprus: (B) E. breviceps; (C) E. janaleeae; (D) E. reginae; (E) E. taeniurus; (F) E. thyphlus. Photographs by A. Catenazzi (A, E) and P. Venegas (B, C, D, F).
FIGURE 4 in Arcanumophis, a new genus and generic allocation for Erythrolamprus problematicus (Myers 1986), Xenodontinae (Colubridae) from the Cordillera de Carabaya, southern Peru
FIGURE 4. Head of Arcanumophis problematicus (CORBIDI 18731), showing horizontal crease on rostrum. Photographs by A. Catenazzi.
FIGURE 1 in Arcanumophis, a new genus and generic allocation for Erythrolamprus problematicus (Myers 1986), Xenodontinae (Colubridae) from the Cordillera de Carabaya, southern Peru
FIGURE 1. Map of southern Peru showing the type locality at San Juan del Oro, Province of Sandia (red square), and the new locality at the abandoned mine of Santo Domingo, Province of Carabaya (white circle), both locations in Department of Puno.
FIGURE 6 in Arcanumophis, a new genus and generic allocation for Erythrolamprus problematicus (Myers 1986), Xenodontinae (Colubridae) from the Cordillera de Carabaya, southern Peru
FIGURE 6. Phylogenetic tree of concatenated partial sequences of two mitochondrial genes (12S and 16S rRNA) of Arcanumophis problematicus and sampled species of Xenodontini.
FIGURE 3 in Arcanumophis, a new genus and generic allocation for Erythrolamprus problematicus (Myers 1986), Xenodontinae (Colubridae) from the Cordillera de Carabaya, southern Peru
FIGURE 3. Coloration in life of Arcanumophis problematicus (CORBIDI 18731) from Santo Domingo, Department of Puno, Peru. Photographs by A. Catenazzi.
FIGURE 2 in Arcanumophis, a new genus and generic allocation for Erythrolamprus problematicus (Myers 1986), Xenodontinae (Colubridae) from the Cordillera de Carabaya, southern Peru
FIGURE 2. Full body of Arcanumophis problematicus CORBIDI 18731 showing dorsal and ventral coloration patterns (pre- served specimen). Photographs by A. Catenazzi.
FIGURE 4. Malesherbia hybrids. a in Notes on Malesherbia (Passifloraceae) in Peru: a new species from southern Peru, a new record and a first report on interspecific hybridization in Malesherbia
FIGURE 4. Malesherbia hybrids. a. Malesherbia fatimae × tenuifolia, inflorescence (M. Weigend et al. 9370); b. Malesherbia fatimae × tenuifolia, leaves (M. Weigend et al. 9370); c. Profesora Fatima Cáceres Huamaní with a bunch of Malesherbia fatimae × tenuifolia and Malesherbia tenuifolia; d. Inflorescence of Malesherbia arequipensis (left), M. ardens (right), Malesherbia ardens × arequipensis (middle; same collections as in e, f, and g); e. Leaves of M. ardens (M. Weigend et al. 7866); f. Leaves of M. ardens × arequipensis (M. Weigend et al. 7868). g. Leaves of M. arequipensis (M. Weigend et al. 7865).
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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
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.