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888 results for “Canary”
FIGURES 23–24 in Review of the genus Agonochaetia Povolný (Lepidoptera, Gelechiidae), and description of a new genus and species from the Canary Islands
FIGURES 23–24. Genitalia terms and abbreviations used in this study. 23, male genitalia; 24, female genitalia. AAL = anterior apophysis length; COE = caecum phalli length; CUL = cucullus length; GLL = glandiductor length; PHL = phallus length; S8L = sternum VIII length; SAL = saccus length; SIB = signum base; SIH = signum hook; TGL = tegumen length; TGN = tegumen notch; UNL= Uncus length; VIN = vinculum anterior notch.
FIGURES 17–22 in Review of the genus Agonochaetia Povolný (Lepidoptera, Gelechiidae), and description of a new genus and species from the Canary Islands
FIGURES 17–22. Abdominal segments; 17–20, segments 1–2; 21–22, segment 8. 17, Gnorimoschema septentrionella Fyles (slide MIC 7717); 18, Symmetrischema costaricanum Povolný (slide MIC 7711); 19, Agonochaetia conspersa (slide MIC 6094); 20, Canarischema fuerteventura (slide JFL 1755); 21, Agonochaetia conspersa (slide MIC 6094); 22, Canarischema fuerteventura (slide JFL 1755). Scale bars = 500 µm. Red arrows indicate the marginosclerite of T1.
FIGURES 37–39 in Review of the genus Agonochaetia Povolný (Lepidoptera, Gelechiidae), and description of a new genus and species from the Canary Islands
FIGURES 37–39. Female genitalia of Agonochaetia species. 37, A. impunctella ♀ (HT) (slide 176452/4220, K.T. Park 1996); 38, A. intermedia ♀ (slide GU 87/107, P. Huemer); 39, A. quartana ♀ (HT) (slide 3222 Povolný),
FIGURES 25–28 in Review of the genus Agonochaetia Povolný (Lepidoptera, Gelechiidae), and description of a new genus and species from the Canary Islands
FIGURES 25–28. Intact male genitalia, ventral and lateral aspects. 25–26, Agonochaetia conspersa (dissection USNM 142571); 27–28, Canarischema fuerteventura (dissection MIC 7845)
FIGURES 4a–o in Song dialects as diagnostic characters - acoustic differentiation of the Canary Island Goldcrest subspecies Regulus regulus teneriffae Seebohm 1883 and R. r. ellenthalerae Päckert et al. 2006 (Aves: Passeriformes: Regulidae)
FIGURES 4a–o. Territorial song of Regulus regulus teneriffae, song types indicated on the sonagrams, lower left. La Gomera: a–d, song type A, strophes of four different males; Tenerife: e, g–h, song type A1 withfixed motiv I, strophes of three different males; f, rare song type F; i, song type B, male from Esperanza Forest; k–m, song type B, three different males from Anaga Mts; n, song type C, male from Anaga Mts; o, song type D, male from Anaga Mts.
FIGURE 2 in Song dialects as diagnostic characters - acoustic differentiation of the Canary Island Goldcrest subspecies Regulus regulus teneriffae Seebohm 1883 and R. r. ellenthalerae Päckert et al. 2006 (Aves: Passeriformes: Regulidae)
FIGURE 2. Distribution of Gold and Firecrests on the Atlantic islands. Distribution of dialect song types from the Canary Islands is indicated by symbols on the according island.
FIGURES 1a–d in Song dialects as diagnostic characters - acoustic differentiation of the Canary Island Goldcrest subspecies Regulus regulus teneriffae Seebohm 1883 and R. r. ellenthalerae Päckert et al. 2006 (Aves: Passeriformes: Regulidae)
FIGURES 1a–d. Vocalization pattern of Goldcrests; a, bipartite song of European Goldcrests, R. r. regulus, Czech Republik; b, tripartite song of R. r. azoricus, São Miguel; syntax: introduction (unit 1) + mid part (ascending phrase, unit 2) + final part (terminal flourish, unit 3); c, parameters measured in sonagraphic analysis indicated by horizontal and vertical lines; d, subsong of R. r. japonensis, Far East Siberia; from a continuous performance of about two minutes.
FIGURE 3 in Song dialects as diagnostic characters - acoustic differentiation of the Canary Island Goldcrest subspecies Regulus regulus teneriffae Seebohm 1883 and R. r. ellenthalerae Päckert et al. 2006 (Aves: Passeriformes: Regulidae)
FIGURE 3. Scatterplot of discriminant function 1 vs. function 2 for subunits of main song part of Canarian Goldcrest dialects and for subsong trills.
FIGURES 5a–o in Song dialects as diagnostic characters - acoustic differentiation of the Canary Island Goldcrest subspecies Regulus regulus teneriffae Seebohm 1883 and R. r. ellenthalerae Päckert et al. 2006 (Aves: Passeriformes: Regulidae)
FIGURES 5a–o. Territorial song of Regulus regulus ellenthalerae, song types indicated on the sonagrams, lower left. El Hierro: a–b, song type A2 with interposed element (arrows) between units 1 and 2, two different males; c–g, song type E with two local rhythmic motifs of unit 2, three different males; h) variation of type A with calllike elements; La Palma: i–o, song type F with more or less extended ascending unit 2 consisting of diverse modulated element types, five different males (i, k: two strophes of one male).
FIGURE 2. Lichenodiplis anomalus, holotype. A in New species of lichenicolous fungi from the Canary Islands
FIGURE 2. Lichenodiplis anomalus, holotype. A. Habit; scale: 125 µm. B. Pycnidial wall and conidiogenuous cells (in water); scale: 10 µm. C–D. Conidiogenous cells and conidia (in Congo Red); scale: 10 µm.
FIGURE 1. Leightoniomyces canariensis, holotype. A in New species of lichenicolous fungi from the Canary Islands
FIGURE 1. Leightoniomyces canariensis, holotype. A. Habit; scale: 0.25 mm. B. Synnema; scale: 100 µm. C-D. Conidiogenous cells and conidia; scale: 10 µm.
FIGURE 3. Perigrapha phaeophysciae, holotype. A-B in New species of lichenicolous fungi from the Canary Islands
FIGURE 3. Perigrapha phaeophysciae, holotype. A-B. Habit; scale: 1 mm. C. Section through multilocular stroma; scale: 100 µm. D. Ascus with ascospores; scale: 25 µm. E. Ascospores; scale: 10 µm.
FIGURE 3. A–C in Micromeria tenensis (Lamiaceae), a new species from Tenerife, Canary Islands
FIGURE 3. A–C. Micromeria tenensis, flowering branches (A), leaf, abaxial (B), and calyx (C). D–F. M. tragothymus, flowering branches (D), leaf, abaxial (E), and calyx (F). Scale bars indicate 2 mm for leaves and 1 mm for calyces. Photos and drawings by P. Puppo.
FIGURE 1. A in Micromeria tenensis (Lamiaceae), a new species from Tenerife, Canary Islands
FIGURE 1. A. Map of Tenerife showing distribution of Micromeria tenensis in Teno (blue) and M. tragothymus in Anaga (dark grey); Dashed lines indicate remnants of paleo-islands; Triangles and black dots indicate collections made in July 2023. B–D. Micromeria tenensis, habitat (B), habit (C), and detail of flowering branch (D). Photos taken by P. Puppo.
FIGURE 1 in Rediscovery of the Canary Islands endemic Aphaenogaster hesperia Santschi, 1911 (Hymenoptera, Formicidae, Myrmicinae)
FIGURE 1. Map showing the geographic position of the Canary Islands (A) and the sampling site and type locality within Tenerife (B). Type locality (Bajamar) is marked with a red polygon and new locality (Las Raíces) is marked with a red dot (C).
FIGURE 3 in Rediscovery of the Canary Islands endemic Aphaenogaster hesperia Santschi, 1911 (Hymenoptera, Formicidae, Myrmicinae)
FIGURE 3. Sampling sites. (A) Nitrophilous community in Bajamar (type locality). (B) Pine forest of Las Raíces (new locality). (C) Detail of the brood chamber, Aphaenogaster hesperia workers can be seen carrying larvae.
Genetic data from the extinct giant rat from Tenerife (Canary Islands)
<p>Evolution of vertebrate endemics in oceanic islands follows a predictable pattern, known as the island rule, according to which gigantism arises in originally small-sized species and dwarfism in large ones. Species of extinct insular giant rodents are known from all over the world. In the Canary Islands, two examples of giant rats, <em>Canariomys bravoi </em>and <em>Canariomys tamarani</em>, endemic to Tenerife and Gran Canaria islands, respectively, disappeared soon after human settlement. The highly derived morphological features of these insular endemic rodents hamper the identification of their mainland relatives and the reconstruction of their evolutionary histories. We have retrieved partial mitochondrial (mtDNA) data from <em>C. bravoi</em> and used this information to explore its evolutionary history. The resulting dated phylogeny confidently places <em>C. bravoi</em> within the African grass rat clade (<em>Arvicanthis niloticus</em>). The estimated divergence time, 650,000 years ago, is roughly coincident with the onset of the Günz-Mindel interglacial stage. <em>C. bravoi</em> ancestors would have reached the island via passive rafting and then underwent a yearly increase of mean body mass calculated between 0.0015 g and 0.0023 g; this corresponds to fast evolutionary rates (in darwins [d], ranging from 7.09 d to 2.78 d) that are well above those observed for non-insular mammals.</p>
Fig. 5. Combined ITSand trnT-F phylogenybasedonmaximum parsimonyand Bayesian inference. Shadedsectionof thetree highlightsspecies with x in Canary grasses (Phalaris, Poaceae): Molecular phylogenetics, polyploidy and floret evolution
Fig. 5. Combined ITSand trnT-F phylogenybasedonmaximum parsimonyand Bayesian inference. Shadedsectionof thetree highlightsspecies with x = 6, and names shown in bold denote polyploid species. * = nodes collapsed in the strictconsensus maximum parsimony tree. • = unknown chromosome number. Floret types follow the structure defined in Fig. 2. A = annual and P = perennial habit.
Fig. 4. trnT-F in Canary grasses (Phalaris, Poaceae): Molecular phylogenetics, polyploidy and floret evolution
Fig. 4. trnT-F phylogram generated from Bayesian inference. Parsimony bootstrap results are above branches and Bayesian posterior probabilities are below. Shaded section of the tree highlights species with x = 6, and names shown in bold denote polyploid species. * = clade collapsed in the strict consensus maximum parsimony tree. • = unknown chromosome number. Floret types follow Fig. 2. A = annual and P = perennial habit.
Fig. 2 in Canary grasses (Phalaris, Poaceae): Molecular phylogenetics, polyploidy and floret evolution
Fig. 2. Adiagrammatic illustrationof sixfloret typesrecognizablein speciesof Phalaris following Anderson (1961) and Baldini (1995). Notethe central fertile floret and the two lateral sterile lemmas that display successive reduction in size.
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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.