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141 results for “affiliation”
FIGURE 2 in Cryptic speciation: distinguishing serpentine affiliated sister species Navarretia paradoxiclara and N. paradoxinota from N. intertexta (Polemoniaceae)
FIGURE 2. Box plots of variation in floral features among N. intertexta (N. int), N. paradoxiclara (N. p_c.), and N. paradoxinota (N. p_n.). Boxes bound the 25 and 75 percentiles; horizontal line marks the 50 percentile, whiskers extend to the 5 and 95 percentiles with outliers shown as dots. The diamond demarks the mean (horizontal vertices) and standard deviation (vertical vertices).
FIGURE 4 in Cryptic speciation: distinguishing serpentine affiliated sister species Navarretia paradoxiclara and N. paradoxinota from N. intertexta (Polemoniaceae)
FIGURE 4. Map of California, U.S.A., with county borders (gray lines) showing the distribution of Navarretia paradoxiclara (stars with four points) and Navarretia paradoxinota (stars with five points). Serpentine areas are shaded black (derived from 2010 Geologic Map of California; http://www.quake.ca.gov/gmaps/GMC/stategeologicmap.html).
FIGURE 1 in Cryptic speciation: distinguishing serpentine affiliated sister species Navarretia paradoxiclara and N. paradoxinota from N. intertexta (Polemoniaceae)
FIGURE 1. Representative most parsimonious phylograms inferred from analysis of DNA sequence data. Acronyms following species names are correlated to specimens in Appendix 1. Lower case letters ('a' and 'b') following acronyms in Figs. 1B, C indicate multiple copies indicative of either polyploidy (e.g. N. propinqua) or possibly gene duplication or intrapopulation variation among multiple individuals (e.g. N. leucocephala). Total character change (base substitutions and indels) are reconstructed above interior branches (terminal values can be inferred by branch length). Branches not found in all shortest trees are indicated by dotted lines. Bootstrap support values are shown in bold italics below branches. A. One of six trees inferred from concatenated cpDNA sequences. B. One of 32 trees inferred from nrDNA ITS sequences. C. One of six trees inferred from nuclear PI sequences.
FIGURE 3 in Cryptic speciation: distinguishing serpentine affiliated sister species Navarretia paradoxiclara and N. paradoxinota from N. intertexta (Polemoniaceae)
FIGURE 3. Features of Navarretia paradoxiclara (all Johnson, Gowen & Mort 09-032) and N. paradoxinota (all Johnson, Gowen & Mort 09-021), with some comparison to N. intertexta and N. propinqua. All vouchers deposited at BRY unless otherwise indicated. A– D. flowers, top and side views, scale bar = 1 cm. A. N. paradoxiclara. B. N. paradoxinota. C. N. intertexta Gowen 1133, 1134-B. D. N. propinqua Johnson & Johnson 11-076. E–H. Corolla dissections, scale bar = 1 cm. E. N. paradoxiclara. F. N. paradoxinota. G. N. intertexta (left = Gowen 1133; right = Ahart 3453 [CAS]). H. N. propinqua Johnson & Johnson 09-067. I–J. Plant habit (note, either species can have a single leader (I) or be variously branched (J), scale bar = 1 cm. I. N. paradoxiclara. J. N. paradoxinota. K–L. Inflorescence, scale bars = 2 cm. K. N. paradoxiclara. L. N. paradoxinota. M–N. Outer inflorescence bract, N. paradoxiclara, scale bar = 1 cm. M. Adaxial view. N. Lateral view. O–P. Inner inflorescence bract, N. paradoxiclara, scale bar = 1 cm. O. Adaxial view. P. Lateral view. Q. Pollen grain, N. paradoxinota, scale bar = 10 µm. R. mature capsule, N. paradoxinota, scale bar = 1 mm (distal end to the left). S. Partially hydrated seed with thin halo of mucilaginous spiracles, N. paradoxinota, scale bar = 1 mm.
Figure 1 in The generic affiliation of Japanese species of the subfamily Psyllinae (Hemiptera: Psyllidae) with a revised checklist
Figure 1. Characters of Japanese Psyllinae. (A–D, F) Psylla alni (Linnaeus); (E, G) Cacopsylla coccinea (Kuwayama). (A) Head, frontal aspect; (B) left hind leg; (C) apex of metatibia; (D, E) male terminalia, lateral aspect; (F, G) female terminalia, lateral aspect; as, apical spurs of metatibia; bs, basal spine of metatibia; pm, paramere; pr, proctiger. Scale bars 0.25 mm.
FIGURE 1 in Parasites of animals in Papua New Guinea recorded at the National Veterinary Laboratory: a catalogue, historical review and zoogeographical affiliations 3143
FIGURE 1. Map of Papua New Guinea showing the 19 provinces and location of places mentioned in the text.
FIGURE 2 in Phylogeny and affiliation of European Anthomyzidae (Diptera) based on mitochondrial 12S and 16S rRNA
FIGURE 2. Resulting phylogram conducted by Bayesian analyses of the combined 12S and 16S rRNA gene sequences. The posterior probabilities (over 0.50) are shown above the branches.
FIGURE 1 in Phylogeny and affiliation of European Anthomyzidae (Diptera) based on mitochondrial 12S and 16S rRNA
FIGURE 1. Anthomyza gracilis Fallén, 1823, female (Russia: Moscow region), body length 2.8 mm. Photo by D. Gavryushin.
FIGURE 13 in Larval morphology of selected Quedius Stephens, 1829 (Coleoptera: Staphylinidae: Staphylinini) with comments on their subgeneric affiliation
FIGURE 13. Results of the morphological similarity among mature larvae of studied Quedius species. (A) Based on 25 morphological characters (without numbers 4 and 11); (B) based on 27 morphological characters (numbered 1–27); numbers mapped on the branches indicate respective features from list of the characters shared by appropriate species.
FIGURE 9. Q in Larval morphology of selected Quedius Stephens, 1829 (Coleoptera: Staphylinidae: Staphylinini) with comments on their subgeneric affiliation
FIGURE 9. Q. brevis (A – G) mature larvae, thorax and abdomen. A – C, pro- (A), meso- (B), metanotum (C) in dorsal aspect; D, setae on mesonotum; E – F, apex of setae on mesonotum; G, abdominal segment I and II in dorsal aspect. Abbreviations: I – III, segments; Te, tergite.
FIGURE 6. Q in Larval morphology of selected Quedius Stephens, 1829 (Coleoptera: Staphylinidae: Staphylinini) with comments on their subgeneric affiliation
FIGURE 6. Q. brevis (A – F), Q. fuliginosus (G, H), Q. cruentus (I), Q. microps (J, K), mature larvae, right maxilla in dorsal aspect. A, cardo and stipes with microtrichia (B); C, G, J, maxillary palp; D, E, apex of segment III of maxillary palp; F, apex of right mala; H, K, right mala in dorsal aspect. Abbreviations: I – III, segments of maxillary palp; Cd, cardo; Dmt, dorsal microtrichia; Ma, mala; Mp, maxillary palp; Pf, palpifer; Sa, sensory appendage; So, solenidium; St, stipes.
FIGURE 8. Q in Larval morphology of selected Quedius Stephens, 1829 (Coleoptera: Staphylinidae: Staphylinini) with comments on their subgeneric affiliation
FIGURE 8. Q. fuliginosus (A), Q. brevis (B), Q. cruentus (C, D), Q. cinctus (E – G) mature larvae, fore leg. A – D, segments of fore leg in anterior aspect; E – G, comb of bifurcate setae on tibia with code. Abbreviations: Cb, comb; Cx, coxa; Fe, femur; Tb, tibia; Tr, trochanter; Tu, tarsungulus.
FIGURE 4. Q in Larval morphology of selected Quedius Stephens, 1829 (Coleoptera: Staphylinidae: Staphylinini) with comments on their subgeneric affiliation
FIGURE 4. Q. fuliginosus (A), Q. brevis (B, E, G), Q. mesomelinus (C), Q. microps (D), Q. cinctus (F), mature larvae, right antenna in dorsal aspect. A – D, general view; E, F, sensory appendage of antennal segment III; G, apex of antennal segment IV. Abbreviations: I – IV, antennal segments; Sa, sensory appendages; So, solenidium.
FIGURE 7. Q in Larval morphology of selected Quedius Stephens, 1829 (Coleoptera: Staphylinidae: Staphylinini) with comments on their subgeneric affiliation
FIGURE 7. Q. brevis (A, B), Q. microps (C), Q. mesomelinus (D), Q. fuliginosus (E, F), Q. boops (G) mature larvae, labium and hypopharynx. A, prementum with ligula in ventral aspect; B, C, labial palp in ventral aspect; D, E, hypopharynx; F, G, ligula. Abbreviations: I – II, segments of labial palp; Lg, ligula; Lp, labial palp; Pmnt, prementum; Sm, sensillum; Dmt, dorsal microtrichia.
FIGURE 12 in Larval morphology of selected Quedius Stephens, 1829 (Coleoptera: Staphylinidae: Staphylinini) with comments on their subgeneric affiliation
FIGURE 12. Variability in the total number of bifurcate setae on fore tibiae of 30 specimens of Q. cinctus. Numbers in the square brackets indicate the number of specimens; –specimen.
FIGURE 1. Q in Larval morphology of selected Quedius Stephens, 1829 (Coleoptera: Staphylinidae: Staphylinini) with comments on their subgeneric affiliation
FIGURE 1. Q. molochinus (A), Q. cinctus (B), Q. brevis (C), Q. cruentus (D) and Q. microps (E), mature larvae, general view.
Datasheets affiliated with thesis "Understanding the adaptive capacity in Populus tremuloides, a keystone North American tree species"
<p>These datasheets are included in the unpublished thesis chapters of the doctoral thesis "Understanding the adaptive capacity in <em>Populus tremuloides</em>, a keystone North American tree species".</p>
Evidence for maintenance of key components of vocal learning in aging budgerigars despite diminished affiliative social interaction
<p>In some species, the ability to acquire new vocalizations persists into adulthood and may be an important mediator of social interactions. While it is generally assumed that vocal learning persists undiminished throughout the lifespan of these open-ended learners, the stability of this trait remains largely unexplored. We hypothesize that vocal learning exhibits senescence, as is typical of complex cognitive traits, and that this decline may relate to age-dependent changes in sociality. The budgerigar (<em>Melopsittacus undulatus</em>), an open-ended learner which develops new contact call types that are shared with social associates upon joining new flocks, provides a robust assay for measuring the effects of aging on vocal learning ability. We formed captive flocks of 4 previously unfamiliar adult males of the same age class, either "young adults" (6 mo.-1 yr.) or "older adults" (≥ 3 yr.), and concurrently tracked changes in contact call structure and social interactions over time. Older adults exhibited decreased vocal diversity, which may be related to the sparser and weaker affiliative bonds observed in older adults. Older adults, however, displayed equivalent levels of vocal plasticity and vocal convergence compared to young adults, suggesting vocal learning ability is largely maintained into later adulthood in an open-ended learner.</p>
OpenAlex Authors and Affiliations, V2
<p>This is the old, deprecated author data for <a href="https://openalex.org">OpenAlex</a>. In July, 2023, the OpenAlex dataset switched to a new author name disambiguation (V3), and deprecated all old author IDs. This is a data dump of those old author IDs.</p> <p>- Author metadata are included in `authors/**/*.gz` files.</p> <p>- Affiliations---mapping of OpenAlex work IDs to (old) Author IDs---are in the `affiliations_export_20230719T1259/*.gz` files.</p> <p>The files are all gzipped JSON-lines files.</p> <p>See the <a href="https://docs.openalex.org">OpenAlex documentation</a> for more information about OpenAlex and how you can use these files.</p>
Valvular Heart Disease Registry Study in Second Affiliated Hospital of ZheJiang University
ClinicalTrials.gov study NCT03011697. IPD Sharing: Not stated. Countries: 1. Publications: 1.
ScienceDex guides
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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.