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1,245 results for “hypothesis”
FIGURE 4. Phylogenetic hypothesis for 19 in Xyela fusca spec. nov. from Japan elucidates East Asian – North American relationships of Xyela (Hymenoptera, Xyelidae)
FIGURE 4. Phylogenetic hypothesis for 19 species of Xyela and, as outgroup taxa, five species of Macroxyela, Megaxyela and Pleroneura based on a maximum likelihood analysis of the barcoding section of COI. Values above branches represent maximum likelihood bootstrap clade frequencies. Each specimen is labelled as follows: "Xyela ..."—species name (Xyela '016 China bakeri group', Xyela '021 USA minor group', Xyela '023 USA minor group' and Xyela '024 USA minor group' are provisional names referring to unidentified species classified on species-group level); "DEI-GISHym ..."—unique specimen identifyer; "♀/♂/L"—female/male imago or larva; "ex Pinus …"—pine species from which larva was extracted; "USA- California …"—country and state/province of origin; "658bp/270bp"—length of sequence.
Microevolution Hypothesis of the Obesity Epidemic Dataset
<p>Includes all data used in study titled: "The Microevolutionary Hypothesis of the Obesity Epidemic" including National obesity rates, Maternal Death Rates, Maternal Morality, GDP, calorie intake, physical inactivity, antibiotic use</p>
Sexual dimorphism and female advantage hypothesis in Dianthus plumarius (Caryophyllaceae)
<p>I tested the sexual dimorphism trade-off hypothesis with the gynomonoecious-gynodioecious <i>Dianthus plumarius </i>(Caryophyllaceae). I measured in female and hermaphrodite plants: flower size, nectar volume and concentration, flower lifespan, ovule production, seed number, seed set, and seed weight. Additionally, bagging and pollen supplementation experiments were carried out to evaluate pollen limitation, probability of apomixis, if spontaneous autogamy is possible, and to examine the importance of pollen origin. </p>
FIGURES 45 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 45. Boostrap consensus tree of 100 most parsimonious trees reconstructed (63 informative characters of 42 taxa); bootsrap support values are indicated above branches.
FIGURES 39–40 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 39–40. Paroster michaelseni (third-instar larva): (39) head capsule, dorsal aspect (not all secondary setae represented); (40) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 33–34 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 33–34. Paroster couragei (third-instar larva): (33) head capsule, dorsal aspect (not all secondary setae represented); (34) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 25–26 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 25–26. Paroster microsturtensis (third-instar larva): (25) head capsule, dorsal aspect (not all secondary setae represented); (26) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bars = 0.20 mm.
FIGURES 27–28 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 27–28. Paroster stegastos (third-instar larva): (27) head capsule, dorsal aspect (not all secondary setae represented); (28) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bars = 0.20 mm.
FIGURES 17–18 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 17–18. Paroster darlotensis, metathoracic leg (third-instar larva): (17) anterior aspect; (18) posterior aspect. Scale bar = 0.50 mm.
FIGURES 21–22 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 21–22. Paroster macrosturtensis (third-instar larva): (21) head capsule, dorsal aspect (not all secondary setae represented); (22) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bars = 0.20 mm.
FIGURES 5–9 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 5–9. Paroster darlotensis (first-instar larva), head appendages: (5) mandible, dorsal aspect; (6–7) maxilla, (6) dorsal aspect; (7) ventral aspect; (8–9) labium; (8) dorsal aspect; (9) ventral aspect. LA, labium; MN, mandible; MX, maxilla. Numbers and lowercase letters refer to primary setae and pores, respectively. Scale bars = 0.10 mm.
FIGURES 23–24 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 23–24. Paroster mesosturtensis (third-instar larva): (23) head capsule, dorsal aspect (not all secondary setae represented); (24) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bars = 0.20 mm.
FIGURES 1–2 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 1–2. Paroster darlotensis (first-instar larva), head capsule: (1) dorsal aspect; (2) ventral aspect. EB, egg bursters: FR, frontoclypeus; PA, parietale; TP, tentorial pits. Numbers and lowercase letters refer to primary setae and pores, respectively. Scale bar = 0.20 mm.
FIGURES 3–4 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 3–4. Paroster darlotensis (first-instar larva), antenna: (3) ventral aspect; (4) dorsal aspect. AN, antenna. Numbers and lowercase letters refer to primary setae and pores, respectively. Scale bar = 0.10 mm.
FIGURES 43–44 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 43–44. Paroster nigroadumbratus (third-instar larva): (43) head capsule, dorsal aspect (not all secondary setae represented); (44) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 41–42 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 41–42. Paroster niger (third-instar larva): (41) head capsule, dorsal aspect (not all secondary setae represented); (42) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 19–20 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 19–20. Paroster hinzeae (third-instar larva): (19) head capsule, dorsal aspect (not all secondary setae represented); (20) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bars = 0.50 mm.
FIGURES 37–38 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 37–38. Paroster insculptilis (third-instar larva): (37) head capsule, dorsal aspect (not all secondary setae represented); (38) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 31–32 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 31–32. Paroster baylyi (third-instar larva): (31) head capsule, dorsal aspect (not all secondary setae represented); (32) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 35–36 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 35–36. Paroster couragei, metathoracic leg (third-instar larva): (35) anterior aspect; (36) posterior aspect. Scale bar = 0.20 mm.
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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.