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291 results for “monophyletic”
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.
FIGURES 29–30 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 29–30. Paroster wedgeensis (third-instar larva): (29) head capsule, dorsal aspect (not all secondary setae represented); (30) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 12–14 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 12–14. Paroster darlotensis (first-instar larva): (12–13) abdominal segment eight; (12) dorsal aspect; (13) ventral aspect; (14) urogomphus, dorsal aspect; AB, abdominal segment eight; UR, urogomphus. Numbers and lowercase letters refer to primary setae and pores, respectively. Scale bars = 0.10 mm.
FIGURES 10–11 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 10–11. Paroster darlotensis (first-instar larva), metathoracic leg: (10) anterior aspect; (11) posterior aspect. CO, coxa; FE, femur; PT, pretarsus; TA, tarsus; TI, tibia; TR, trochanter. Setae PT1 and PT2 not represented. Numbers and lowercase letters refer to primary setae and pores, respectively. Scale bar = 0.10 mm.
FIGURES 15–16 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 15–16. Paroster darlotensis (third-instar larva): (15) head capsule, dorsal aspect (not all secondary setae represented); (16) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bars = 0.50 mm.
FIGURE 39 in Cleonini (Coleoptera: Curculionidae: Lixinae) are monophyletic and flightless: tribe overview, rampant adult homoplasy and illustrated global diversity
FIGURE 39. Cleonini, adults, claws, dorsal view. A: Adosomus (Adosomus) roridus; B: Afghanocleonus haarloevi; C: Ammocleonus hieroglyphus; D: Bothynoderes declivis; E: Gonocleonus margaritiferus; F: Isomerops fausti; G: Leucochromus imperialis; H: Maximus strabus; I: Pleurocleonus quadrivittatus; J: Terminasiania granosa; K: Trichocleonus leucophyllus.
A new phylogenetic hypothesis for Cereinae (Cactaceae) points to a monophyletic subtribe
<p>Cereinae comprises 14 genera distributed in Neotropical dry forest formations such as in the Caatingas of Northeastern or in rocky outcrops in the north of Southeastern Brazil. Historically, the taxonomy of the group has been very controversial, especially regarding generic circumscriptions, and phylogenetic relationships within the group are still poorly understood. To investigate the delimitation of the subtribe and infra-subtribal relationships, we performed a phylogenetic analysis including 50 taxa representing 13 genera using one nuclear (<i>PhyC</i>) and four cpDNA (<i>petL-psbE</i>, <i>trnL-trnT</i>, <i>trnS-trnG</i>, and <i>rpl16</i>) regions. Our results show a monophyletic Cereinae with high support in Bayesian, maximum parsimony, and maximum likelihood analyses based on combined matrices. Although our results expand the knowledge of generic relationships, we emphasize the need for further molecular phylogenetic studies combined with ecological evidence to clarify relationships at the more inclusive nodes of the subtribe.</p>
FIGURE 46 in Cleonini (Coleoptera: Curculionidae: Lixinae) are monophyletic and flightless: tribe overview, rampant adult homoplasy and illustrated global diversity
FIGURE 46. Cleonini weevils, adults, ♀s, spermatheca. A: scheme; B: Adosomus (Adosomus) roridus; C: Ammocleonus aschabadensis; D: Asinocleonus taciturnus; E: Asproparthenis punctiventris; F: Coniocleonus (Angarocleonus) astragali; G: Coniocleonus (Plagiographus) crinipes; H: Conorhynchus pulverulentus; I: Leucochromus imperialis; J: Leucomigus candidatus; K: Neocleonus sannio; L: Pachycerus madidus; M: Porocleonus candidus; N: Pseudocleonus (Neopseudocleonus) grammicus; O: Surchania sijaZovi.
FIGURE 43 in Cleonini (Coleoptera: Curculionidae: Lixinae) are monophyletic and flightless: tribe overview, rampant adult homoplasy and illustrated global diversity
FIGURE 43. Cleonini weevils, adults, ♂s, endophallus, lateral view. A: Adosomus (Adosomus) roridus; B: Ammocleonus aschabadensis; C: Asproparthenis punctiventris; D: Bothynoderes affinis; E: Brachycleonus fronto; F: Chromonotus (Chromonotus) vittatus; G: Chromosomus fischeri; H: Cleonis japonica; I: Coniocleonus (Plagiographus) nigrosuturatus; J: Conorhynchus pulverulentus; K: Epexochus lehmanni; L: Eumecops kittaryi; M: Leucomigus candidatus; N: Liocleonus clathratus; O: Maximus strabus; P: Menecleonus lagopus; Q: Monolophus praeditus; R: Porocleonus candidus; S: Pseudocleonus (Pseudocleonus) cinereus; T: Scaphomorphus vibex; U: Stephanocleonus (Deracanthopsis) gemellus; V: Surchania sijaZovi; W: Temnorhinus (Temnorhinus) hololeucus; X: Xanthochelus eversmanni.
FIGURE 40 in Cleonini (Coleoptera: Curculionidae: Lixinae) are monophyletic and flightless: tribe overview, rampant adult homoplasy and illustrated global diversity
FIGURE 40. Scanning electron microscopy images of scales, dorsal surface of right elytron in basal third. A: Entymetopus (Entymetopus) lineolatus; B: Eumecops kittaryi; C: Liocleonus clathratus; D: Lixomorphus algirus; E: Mongolocleonus gobiensis; F: Prionorhinus canus; G: Tetragonothorax lyali; H: Trichocleonus leucophyllus.
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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.