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2,331 results for “Andean”
FIGS. 100–111. 100–105 in The Andean Goblin Spiders of the New Genus Scaphidysderina (Araneae, Oonopidae), With Notes on Dysderina
FIGS. 100–111. 100–105. Scaphidysderina tapiai, new species, female. 106–111. S. pinocchio, new species, female. 100,106. Carapace, anterior view. 101, 107. Abdomen, lateral view. 102, 108. Same, ventral view. 103, 109. Epigastric area, ventral view. 104, 110. Digested genitalia, ventral view. 105, 111. Same, dorsal view.
FIGS. 74–81 in The Andean Goblin Spiders of the New Genus Scaphidysderina (Araneae, Oonopidae), With Notes on Dysderina
FIGS. 74–81. Scaphidysderina loja, new species, female. 74. Carapace, dorsal view. 75. Same, anterior view. 76. Sternum and mouthparts, ventral view. 77. Abdomen, lateral view. 78. Same, ventral view. 79. Epigastric area, ventral view. 80. Digested genitalia, ventral view. 81. Same, dorsal view.
FIGS. 66–73 in The Andean Goblin Spiders of the New Genus Scaphidysderina (Araneae, Oonopidae), With Notes on Dysderina
FIGS. 66–73. Scaphidysderina tayos, new species, female. 66. Carapace, dorsal view. 67. Same, anterior view. 68. Sternum and mouthparts, ventral view. 69. Abdomen, lateral view. 70. Same, ventral view. 71. Epigastric area, ventral view. 72. Digested genitalia, ventral view. 73. Same, dorsal view.
FIGS. 90–99 in The Andean Goblin Spiders of the New Genus Scaphidysderina (Araneae, Oonopidae), With Notes on Dysderina
FIGS. 90–99. Scaphidysderina tapiai, new species, male. 90. Carapace, dorsal view. 91, 94. Same, anterior view. 92. Chelicerae and endite, lateral view. 93. Sternum and mouthparts, ventral view. 95. Endites, ventral view. 96. Embolus, ventral view. 97. Left palp, prolateral view. 98. Same, ventral view. 99. Same, retrolateral view.
FIGS. 37–48 in The Andean Goblin Spiders of the New Genus Scaphidysderina (Araneae, Oonopidae), With Notes on Dysderina
FIGS. 37–48. Scaphidysderina pagoreni, new species, male (37–46) and female (47, 48). 37. Carapace, dorsal view. 38, 43. Same, anterior view. 39. Sternum and mouthparts, ventral view. 40. Left palp, prolateral view. 41. Same, ventral view. 42. Same, retrolateral view. 44. Labium and endites, ventral view. 45. Embolus, retrolateral view. 46. Same, ventral view. 47. Chelicerae, anterior view. 48. Same, posterior view.
Fig. 3 in Trechisibus apukhapiensis sp. n. (Coleoptera: Carabidae, Trechinae) from southeastern Andean mountains of Peru
Fig. 3. Location of the Trechisibus species (= T. apukhapiensis, A= T. bohorquezae, B=T. cuzcoensis, C=T. gigas, D=T. nicki, E=T. theresiae, F=T. franzi, G=T. schmidti, H=T. laresensis, I=T. veneroi, J=T. orophilus, K=T. peruvianus, L= T. ukupachensis, M=T. wardi, N= T. pygmaeus).
Figure 5. Eremophygus philippii Ohaus. A–F in Revision of the high Andean genus Eremophygus Ohaus (Coleoptera: Scarabaeidae: Rutelinae: Rutelini)
Figure 5. Eremophygus philippii Ohaus. A–F) Male lectotype of Eremophygus philippii Ohaus. A) Habitus, dorsal view. B) Habitus, lateral view. C) Labels. D–E) Aedeagus. D) Dorsal view. E) Lateral view. F) Mentum, ventral view. G–I) Male holotype of Eremophygus leo Gutiérrez (= E. philippi). G) Habitus, dorsal view. H) Habitus, lateral view. I) Labels.
Figure 4. Eremophygus lasiocalinus Ohaus. A–C in Revision of the high Andean genus Eremophygus Ohaus (Coleoptera: Scarabaeidae: Rutelinae: Rutelini)
Figure 4. Eremophygus lasiocalinus Ohaus. A–C) Male holotype of Eremophygus bicolor (Gutiérrez) (=E. lasiocalinus). A) Habitus, dorsal view. B) Habitus, lateral view. C) Labels. D–F) Female lectotype of Eremophygus pachyloides Ohaus (=female E. lasiocalinus). D) Habitus, dorsal view. E) Habitus, lateral view. F) Lectotype labels, egg, and mouthparts. G–L) Male lectotype of Eremophygus lasiocalinus Ohaus. G) Habitus, dorsal view. H) Habitus, lateral view. I) Labels. J–K) Aedeagus. J) Lateral view. K) Dorsal view. L) Mentum.
Figure 2 in Revision of the high Andean genus Eremophygus Ohaus (Coleoptera: Scarabaeidae: Rutelinae: Rutelini)
Figure 2. Andean habitat of Eremophygus philippii Ohaus in the Antofagasta Mountain range, Chile. Photo courtesy of Andrés Ramírez C.
Figure 1 in Revision of the high Andean genus Eremophygus Ohaus (Coleoptera: Scarabaeidae: Rutelinae: Rutelini)
Figure 1. Detailed morphology of the genus Eremophygus Ohaus, 1910. A–B) Antenna. A) Female. B) Male. C) Head in dorsal view. D) Left maxilla, lateral view. E) Mentum, ventral view. F) Protarsus of male, lateral view.
Floral phenology of an Andean bellflower and pollination by Buff-tailed Sicklebill
<p class="MsoNormal"><span>The Andean bellflowers comprise an explosive radiation correlated with shifts to specialized pollination. One diverse clade has evolved with extremely curved floral tubes and are predicted to be pollinated exclusively by one of two parapatric species of Sicklebill hummingbirds (<em>Eutoxeres</em>). In this study we focused on the floral biology of <em>Centropogon granulosus</em>, a bellflower thought to be specialized for pollination by <em>E. condamini</em>, in a montane cloud forest site in southeastern Peru. Using camera traps and a pollination exclusion experiment, we documented <em>E. condamini</em> as the sole pollinator of <em>C.granulosus</em>. Visitation by <em>E. condamini</em> was necessary for fruit development. Flowering rates were unequivocally linear and conformed to the 'steady state' phenological type. Over the course of >1800 hours of monitoring we recorded 12 <em>E. condamini</em> visits totaling 42 seconds, indicating traplining behaviour. As predicted by its curved flowers, <em>C. granulosus</em> is exclusively pollinated by Buff-tailed Sicklebill within our study area. We present evidence for the congruence of phenology and visitation as a driver of specialization in this highly diverse clade of Andean bellflowers.</span></p>
Constraining Andean Propagation of Exhumation at the Limit of the Eastern Cordillera, NW Argentina, using Low-Temperature Thermochronology in a Structural Context - Supporting Information
<p>Supporting information accompanying the publication "Constraining Andean Propagation at the Limit of the Eastern Cordillera, NW Argentina, using Low-Temperature Thermochronology in a Structural Context" published in Tectonics. The dataset contains apatite and zircon (U-Th-Sm)/He and apatite fission track data from the Tilcara Range and San Lucas block, Jujuy, Argentina, as well as additional QTQt thermal models that are discussed in the paper.</p> <p>Table S1 contains full single-grain results from apatite fission track, apatite (AHe) (U-Th-Sm)/He and zircon (ZHe) (U-Th-Sm)/He analyses. Outliers are marked in grey and are not included in the weighted mean age. Figure S1 supports (U-Th-Sm)/He data graphically. Apatite fission track (AFT) data is supported by radial plots in Figure S2. Figure S3 shows QTQt thermal models using either AHe, AFT or ZHe single-grain ages. All of the models results are explained in the main text.</p>
Fig. 2 in Morphological description of Pintomyia (Pifanomyia) veintemillaSi n. sp., a new sand fly species from the sub-Andean region of Bolivia
Fig. 2 Pintomyia (Pif.) veintemillasi n. sp. female. a head frontal view; b antennomer fII; c cibarium and pharynx; d cibarium; e laciniae of the maxillae; f sternite 2; g spermatheca; h rapid view of a complete genitalia; i wing. Scales are in mm
Fig. 1 in Morphological description of Pintomyia (Pifanomyia) veintemillaSi n. sp., a new sand fly species from the sub-Andean region of Bolivia
Fig. 1 Pintomyia (Pif.) veintemillasi n. sp. male. a Head frontal view; b antennomer fII; c cibarium and pharynx; d sternite 2; e genitalia profile; f paramere and aedeagus, in lateral view; g genital pump and genital filaments; h wing. Scales are in mm
Fig. 3 in Morphological description of Pintomyia (Pifanomyia) veintemillaSi n. sp., a new sand fly species from the sub-Andean region of Bolivia
Fig. 3 Comparative representation showing the pigmentation of the thorax profile of females (scale is in mm): a Pi. (Pif.) maranonensis; b Pi. (Pif.) veintemillasi; c Pi. (Pif.) nevesi
FIGURE 4 in Species delimitation reveals an underestimated diversity of Andean catfishes of the family Astroblepidae (Teleostei: Siluriformes)
FIGURE 4 | Species tree inferred from the concatenated dataset of mitochondrial genes (COI, Cytb, and 16S). Nodal support values are Bayesian posterior probabilities. Non-significant speciation probabilities identified in BP&P analysis algorithm A10 (PP:<0.95) are indicate by black circles and species supported with asterisk.
FIGURE 2 in Species delimitation reveals an underestimated diversity of Andean catfishes of the family Astroblepidae (Teleostei: Siluriformes)
FIGURE 2 | Map of northwestern South America showing the geographic distribution of samples used in this study and species distribution of Astroblepus reported in Global Biodiversity Information Facility (GBIF) and the California Academy of Sciences (CAS) databases.
FIGURE 1 in Species delimitation reveals an underestimated diversity of Andean catfishes of the family Astroblepidae (Teleostei: Siluriformes)
FIGURE 1 | Species of Astroblepus included in this study, A. A. ardiladuartei (LBP 26696 topotype live, 4.54 mm SL), B. A. cachara (LBP 26712 topotype live, 4.23 mm SL), C. A. caquetae (CZUT-IC 18464 topotype of museum, 7.84 mm SL), D. A. curitiensis (LBP 97118 topotype live, 5.92 mm SL), E. A. homodon (CZUT-IC 18390, 6.15 mm SL), F. A. gr. grixalvii (LBP24242 topotype live, 11.70 mm SL); F'. A. gr. grixalvii (CZUT-IC 18498 specimen of Magdalena basin 6,01 mm SL); F". A. gr. grixalvii (CZUT-IC 18320 specimen of Cauca basin, 15.25 mm SL), G. A. itae (topotype live, 3.58 mm SL), H. A. latidens (topotype live, 13.40 mm SL), I. A. onzagaensis (topotype live, 7.82 mm SL), J. A. pradai (topotype live, 4.53 mm SL), K. A. trifasciatus (topotype of museum, 9.65 mm SL), K'. A. trifasciatus (topotype of museum, 9.01 mm SL), L. A. aff. trifasciatus (specimen of Magdalena basin, 7.94 mm SL), M. A. verai (topotype live, 3.51 mm SL).
FIGURE 3 in Species delimitation reveals an underestimated diversity of Andean catfishes of the family Astroblepidae (Teleostei: Siluriformes)
FIGURE 3 | Results of single-locus approaches using cytochrome oxidase c subunit I (COI) for developing preliminary species delimitation hypothesis with 42 lineages. Results are represented on the ultrametric gene tree with collapsed nodes. All nodal support values were PP>0.95. Blocks at right of the tree represent hypothesized species groups and the values in the middle indicate the number of clusters identified by ABGD, bPTP and GMYC analyses for every collapsed node. COL: Colombia, ECU: Ecuador, PER: Peru.
Figure 5 in A new species of Andean lizard Proctoporus (Squamata: Gymnophthalmidae) from montane forest of the Historic Sanctuary of Machu Picchu, Peru
Figure 5. Type locality of Proctoporus machupicchu: (A, C) Montane forest, (B) Urubamba River, (D) Habitat of Proctoporus machupicchu. Photo: (6 A–C) Luis Mamani; 6 D (Javier Farfan).
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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.