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1,709 results for “Reflectivity”
Figure 2. Amaga amagensis. NHM 1928 in Reflections on the genus Amaga Ogren and Kawakatsu 1990, and description of a new genus of land planarian (Platyhelminthes: Tricladida: Geoplanidae)
Figure 2. Amaga amagensis. NHM 1928. (A) Sagittal reconstruction of copulatory apparatus of specimen B. (B) Sagittal reconstruction of copulatory apparatus of specimen A. See text for abbreviations.
Figure 5 in Reflections on the genus Amaga Ogren and Kawakatsu 1990, and description of a new genus of land planarian (Platyhelminthes: Tricladida: Geoplanidae)
Figure 5. Bogga bogotensis. (A) NHW 2741, sagittal section of copulatory apparatus. Gaps in dorsal and ventral epidermis due to composite nature of the photograph. (B) ZMA V.Pl. 6904.1, sagittal section of copulatory apparatus. (C) ZMA V.Pl. 6904.1, sagittal reconstruction of copulatory apparatus. (D) Holotype ZMB 743, sagittal reconstruction of copulatory apparatus. See text for abbreviations.
Figure 4 in Reflections on the genus Amaga Ogren and Kawakatsu 1990, and description of a new genus of land planarian (Platyhelminthes: Tricladida: Geoplanidae)
Figure 4. Bogga bogotensis. (A) Holotype ZMB 743. Transverse section of the pre-pharyngeal region. (B) ZMA V.Pl. 6904.1, transverse section of the pre-pharyngeal region. (C) Holotype ZMB 743, sagittal reconstruction of pharynx. See text for abbreviations.
Figure 3 in Observations on the spectral reflectances of certain high Andean Penaincisalia and Thecloxurina, with the description of a new species (Lepidoptera: Lycaenidae: Eumaeini)
Figure 3. Male Thecloxurina terminal aedeagi in same magnification. (A) Thecloxurina tegulina sp. n.; (B) Thecloxurina atymna (Hewitson, 1870) (basal cornuti length 0,003mm).
Figure 4 in Observations on the spectral reflectances of certain high Andean Penaincisalia and Thecloxurina, with the description of a new species (Lepidoptera: Lycaenidae: Eumaeini)
Figure 4. Individual reflectance spectra of Thecloxurina males. (A) Thecloxurina loxurina (Felder and Felder, 1865), black: prov. Antioquia, Colombia (SRMN: 114), red: prov. Valle, Colombia (SRMN 115), green: prov. Pichincha, Ecuador (SRMN: 116), blue: prov. Morona-Santiago, Ecuador (SRMN: 105); (B) Thecloxurina chachapoya Bálint and Wojtusiak, 2003 from Peru, black: dep. Amazonas (SRMN: 108), red and green: dep. Apurímac (SRMN: 109–110); (C) Thecloxurina atymna (Hewitson, 1870) from Ecuador, black: prov. Tungurahua (SRMN: 118), red: prov. Pincincha (SRMN: 119), green: prov. Zamora (SRMN: 120); (D) Thecloxurina tegulina sp. n., black: holotype (SRMN: 101), red: paratype 1 (SRMN: 102), green: paratype 2 (SRMN: 103); Thecloxurina cillutincarae (Draudt, 1919), blue: dep. Puno (SRMN: 100).
Figure 2 in Observations on the spectral reflectances of certain high Andean Penaincisalia and Thecloxurina, with the description of a new species (Lepidoptera: Lycaenidae: Eumaeini)
Figure 2. Male Thecloxurina dorsal forewing androconia with scent pad and scent patch. (A) Thecloxurina. tegulina sp. n.; (B) Thecloxurina atymna (Hewitson, 1870); (C) Thecloxurina chachapoya Bálint and Wojtusiak, 2003; (D) Thelcoxurina. cillutincarae (Draudt, 1919).
Figure 5 in Observations on the spectral reflectances of certain high Andean Penaincisalia and Thecloxurina, with the description of a new species (Lepidoptera: Lycaenidae: Eumaeini)
Figure 5. Individual reflectance spectra of Penaincisalia males from the Llanganuco valley, Cordillera Blanca, dept. Ancash, Peru, black: Penaincisalia. aurulenta Johnson, 1990 (SRMN: 111), red: Penaincisalia perezi Bálint, 2001 (SRMN: 112), green: Penaincisalia culminicola (Staudinger, 1894) (SRMN: 113).
Figure 1 in Observations on the spectral reflectances of certain high Andean Penaincisalia and Thecloxurina, with the description of a new species (Lepidoptera: Lycaenidae: Eumaeini)
Figure 1. Male Thecloxurina imagines (scale bar: 15 mm). (A) Thecloxurina tegulina sp. n., holotype dorsal view; (B) ditto, ventral view; (C) Thecloxurina atymna (Hewitson, 1870), S Ecuador (prov. Azuay), male, dorsal view; (D) Thecloxurina loxurina (Felder and Felder, 1865), C Peru (dep. Pasco), male, dorsal view; (E) Thecloxurina chachapoya Bálint and Wojtusiak, 2003, C Peru (dep. Cuczo); (F) Thecloxurina cillutincare (Draudt, 1919), S Peru (dep. Puno).
FIGURE 5 in C-heterochromatin variation in the karyotype reflects species level distinction between Erinaceus roumanicus and E. concolor (Eulipotyphla: Erinaceidae) in Turkey
FIGURE 5. NORs distribution in karyotypes of Turkish hedgehogs. A, female of E. concolor from Sinop in northern Anatolia; B, male of E. concolor from Konya and Antalya in central and southern Anatolia; C. male of E. roumanicus from Edirne in Thrace.
FIGURE 4. C in C-heterochromatin variation in the karyotype reflects species level distinction between Erinaceus roumanicus and E. concolor (Eulipotyphla: Erinaceidae) in Turkey
FIGURE 4. C-banded karyotypes of Turkish hedgehogs. A, male of Erinaceus concolor from Konya in central Anatolia; B, male of E. roumanicus from Edirne in Thrace.
FIGURE 1 in C-heterochromatin variation in the karyotype reflects species level distinction between Erinaceus roumanicus and E. concolor (Eulipotyphla: Erinaceidae) in Turkey
FIGURE 1. Collecting localities. () 1. Sinop, 2. Trabzon (north-eastern Turkey – northern Anatolia); () 3, K₁r₁kkale, 4. Konya, 5. Antalya, 6. Gaziantep, 7. Şanl₁urfa (central and southern Anatolia); () 8. Edirne, 9. Tekirdaǧ (European Turkey –Thrace).
Figure 3 in Contemporary genetic structure reflects historical drainage isolation in an Australian snapping turtle, Elseya albagula
Figure 3. Bayesian population assignments for Elseya albagula individuals based on 12 microsatellite loci analysed in STRUCTURE, indicating structure by region and catchment. Individuals are represented by coloured vertical bars, which represent per cent genetic membership (y axis) within genetic units as indicated above each diagram. A, individual differentiation between two regional units (K = 2), and B, further substructuring amongst catchments within the southern region (K = 3). Black lines separate sampling locations, identified below (x axis). B, Burnett, F, Fitzroy; M, Mary.
Figure 3 in Craniid brachiopods: aspects of clade structure and distribution reflect continental drift (Brachiopoda: Craniiformea)
Figure 3. Craniid phylogeny. PAUP* maximum likelihood tree constructed from nuclear LSU rDNA sequences using the best-fitting evolutionary model and showing jackknife clade support (%). In this tree (contrast with Figure 2) the NE Pacific clade is allied to the Tethyan and Northern clades.
Figure 4 in Craniid brachiopods: aspects of clade structure and distribution reflect continental drift (Brachiopoda: Craniiformea)
Figure 4. Craniid phylogeny. Relative age, Bayesian log-likelihood, relaxed-clock time-tree from BEAST, root age defined as 1.0, with inferred relative time-depths of other nodes as shown, or as noted in the Discussion. Confidence intervals (95% highest posterior density) are shown as bars across nodes. Based on SSU+LSU sequences of craniid ingroup and brachiopod and phoronid outgroups.
Convolutional-neural-network-based reflection full-waveform inversion
<p>The data is used by the paper "Convolutional-neural-network-based reflection 1 full-waveform inversion"</p>
Figure 4 in An evolutionary history embedded in amber: reflection of the Mesozoic shift in weevil-dominated (Coleoptera: Curculionoidea) faunas
Figure 4. Photos and drawings of Albicar contriti gen. et sp. nov. (CES–432, holotype), from Early Cretaceous El Soplao amber (Spain). A, photo and camera lucida drawing of the dorsal habitus; B, photo and camera lucida drawing of the lateral habitus, arrow marks the two spurs at the metatibial apex.
Figure 3 in An evolutionary history embedded in amber: reflection of the Mesozoic shift in weevil-dominated (Coleoptera: Curculionoidea) faunas
Figure 3. Photos and drawing of Arra legalovi gen. et sp. nov. (CES–576, paratype), from Early Cretaceous El Soplao amber (Spain). A, camera lucida drawing and photo of the dorsal habitus, arrows mark the seventh funicular article, slightly smaller than the preceding ones; B, ventral habitus; C, lateral habitus.
Figure 2 in An evolutionary history embedded in amber: reflection of the Mesozoic shift in weevil-dominated (Coleoptera: Curculionoidea) faunas
Figure 2. Photo and detail of Arra legalovi gen. et sp. nov. (CPT–4106, holotype), from Early Cretaceous San Just amber (Spain). A, dorsal habitus; B, camera lucida drawing and photo of the metatarsus, showing the partially fused tarsomeres 4 and 5, suture marked with an arrow.
Figure 1. 3D in An evolutionary history embedded in amber: reflection of the Mesozoic shift in weevil-dominated (Coleoptera: Curculionoidea) faunas
Figure 1. 3D reconstruction of Arra legalovi gen. et sp. nov. (CPT–4106, holotype), from Early Cretaceous San Just amber (Spain), using propagation phase-contrast X-ray synchrotron microtomography at beamline ID19, ESRF, Grenoble. A, dorsal habitus; B, right lateral habitus; C, left lateral habitus; D, ventral habitus; E, anterior habitus; F, posterior habitus.
Figure 5. 3D in An evolutionary history embedded in amber: reflection of the Mesozoic shift in weevil-dominated (Coleoptera: Curculionoidea) faunas
Figure 5. 3D reconstruction of Antiquis opaque gen. et sp. nov. (IGR.ARC–331.2, holotype), from mid-Cretaceous, latest Albian or earliest Cenomanian, Font-de-Benon amber (France), using propagation phase-contrast X-ray synchrotron microtomography at beamline ID19, ESRF, Grenoble. A, right lateral habitus; B, dorsal habitus; C, ventral habitus; D, left lateral habitus; E, anterior habitus; F, posterior habitus.
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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.