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14,185 results for “phylogenies”
Figs. 2, 3 in Biology and Immature Stages of the Bee Nomioides patruelis (Halictidae: Halictinae: Nomioidini) and of Its Cleptoparasite, Chiasmognathus pashupati (Apidae: Nomadinae: Ammobatini), with a Preliminary Phylogeny of the Halictidae Based on
Figs. 2, 3. Brood cells of Nomioides patruelis. 2. Front end of cell, inner view, showing deeply concave spiral cell closure; line demarking closure diameter 5 1.5 mm. 3. Approximate longitudinal view with front end at left. Note slight shine of lining on cell wall at left and feces piled on wall at rear end of cell; line demarking cell diameter 5 ca. 2.5 mm.
Figs. 21–25 in Biology and Immature Stages of the Bee Nomioides patruelis (Halictidae: Halictinae: Nomioidini) and of Its Cleptoparasite, Chiasmognathus pashupati (Apidae: Nomadinae: Ammobatini), with a Preliminary Phylogeny of the Halictidae Based on
Figs. 21–25. SEM micrographs of pupa of Nomioides patruelis, approximate anterolateral view. 21. Anterior part of pupa with numbers referring to close-ups in figs. 22–25. 22. Close-up of frons and vertex. 23. Close-up of anterior mesoscutal tubercles. 24. Close-up of mesocutellar, axillary, and metanotal tubercles. 25. Close-up of tegular tubercle.
Figs. 17–20. 17, 18 in Biology and Immature Stages of the Bee Nomioides patruelis (Halictidae: Halictinae: Nomioidini) and of Its Cleptoparasite, Chiasmognathus pashupati (Apidae: Nomadinae: Ammobatini), with a Preliminary Phylogeny of the Halictidae Based on
Figs. 17–20. 17, 18. Diagrams of pupa of Nomioides patruelis, lateral view, entire pupa (with tergal tubercle enlargement), and front end of pupa, dorsal view, respectively. 19, 20. Diagrams of front end of pupa of Chiasmognathus pashupati, dorsal view, and of entire pupa, lateral view, respectively. Scale (5 1.0 mm) refers to all figures.
Fig. 6 in Phylogeny and Taxonomic Revision of Nuchequula Whitley 1932 (Teleostei: Leiognathidae), with the Description of a New Species
Fig. 6. Illustrations: (A) Non-type Indian specimen of Nuchequula blochii from Day (1875). (B) Non-type Australian specimen of Nuchequula decora from Jones (1985). (C) Holotype of Nuchequula nuchalis from Temminck and Schlegel (1845). (D) Holotype of Nuchequula pan from Wongratana (1988).
Fig. 5 in Phylogeny and Taxonomic Revision of Nuchequula Whitley 1932 (Teleostei: Leiognathidae), with the Description of a New Species
Fig. 5. Fresh material from Tonshi Fish Market, Taiwan. (A) Two paratypes of Nuchequula mannusella, new species. (B) Nuchequula nuchalis.
Fig. 4 in Phylogeny and Taxonomic Revision of Nuchequula Whitley 1932 (Teleostei: Leiognathidae), with the Description of a New Species
Fig. 4. Nuchequula mannusella, new species: (A) Holotype, AMNH 238753, 85.5 mm SL, Taiwan. (B) Right side of holotype. (C) Drawing of holotype. (D) Paratype, AMNH 238759, 94.1 mm SL, Taiwan.
Fig. 2 in Phylogeny and Taxonomic Revision of Nuchequula Whitley 1932 (Teleostei: Leiognathidae), with the Description of a New Species
Fig. 2. PCA for species of Nuchequula (plot of PC1 versus PC2). Individuals of Nuchequula mannusella. are represented by black crosses; N. decora (all identified by Jones AMS I.22990002) is represented by squares; and N. nuchalis is represented by triangles. Type specimens are represented by open shapes, including N. blochii syntypes (rectangles) and N. pan paratype (circle). (Only N. pan paratype USNM 276536 is included because the holotype and other paratypes of this species were examined at CUMZ and were not available for this analysis.)
Fig. 1 in Phylogeny and Taxonomic Revision of Nuchequula Whitley 1932 (Teleostei: Leiognathidae), with the Description of a New Species
Fig. 1. Landmarks used for PCA: (1) rostral tip of premaxilla; (2) posterior end of nuchal spine; (3) anterior insertion of dorsal fin; (4) posterior insertion of dorsal fin; (5) dorsal insertion of caudal fin; (6) midpoint of caudal border of hypural plate; (7) ventral insertion of caudal fin; (8) posterior insertion of anal fin; (9) anterior insertion of anal fin; (10) dorsal base of pelvic fin; (11) ventral end of lower jaw articulation; (12) posterior end of maxilla; (13) anterior margin through midline of eye; (14) posterior margin through midline of eye; (15) dorsal end of opercle; (16) dorsal base of pectoral fin. Base figure modified from Nelson (2006).
Fig. 27 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 27. Phylogeny of Eucoilinae after Fontal-Cazalla et al. (2002) with the putative positions of the three Cretaceous amber taxa (Anteucoila, Jerseucoila, and Syneucoila) being noted (support for clades is outlined in table 4).
Fig. 26 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 26. Phylogeny of the Cynipoidea summarizing relationships among major lineages. Fossil records are tabulated in appendix 1. Abbreviations for particular deposits are: Rott (Rott, Germany), Fr (Cantal, France), Wig (Isle of Wight, England), Flor (Florissant, Colorado), Biamo (Biamo, today Bol'shaya Svetlovodnaya), Baltic (Baltic amber), Can (Canadian amber), Sib (Siberian amber of the Taimyr Peninsula), NJ (New Jersey amber), and Obe (Obeshchayushchiy Creek).
Fig. 24 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 24. Character optimization showing unambiguous character changes on internodes of one of the single shortest trees from figure 23 (the two minimal length topologies differ only in relationships within Liopteridae, and thus the subfamilies of this group are collapsed into a single terminal for the purposes of the figure, with those unambiguous character optimizations for the modern liopterid clade being noted). Solid circles indicate unambiguous character transformations; open circles show homoplastic character transformations.
Fig. 25 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 25. Preferred cladogram of cynipoid relationships; character optimization showing unambiguous character changes on internodes of the single shortest tree from figure 21 (the two minimal length topologies differ only in relationships within Liopteridae, and thus the subfamilies of this group are collapsed into a single terminal for the purposes of the figure, with those unambiguous character optimizations for the modern liopterid clade being noted). Solid circles indicate unambiguous character transformations; open circles show homoplastic character transformations.
Fig. 22 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 22. Strict consensus tree of the two shortest trees (L 5 235, CI 5 54, RI 5 79) resulting from analyses of the data matrix (as described in the text and in fig. 20), with the inclusion of two additional Cretaceous amber taxa known only from males (i.e., Tanaoknemus and Micropresbyteria) and no constraints.
Fig. 23 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 23. Strict consensus tree of the two shortest trees (L 5 239, CI 5 55, RI 5 79) resulting from analysis of the data matrix from figure 22 (i.e., with Tanaoknemus and Micropresbyteria included), with the phylogenetic relationship of Anteucoila with the two representative figitids constrained.
Fig. 21 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 21. Preferred set of cladistic relationships among Cynipoidea; strict consensus of the two shortest tree (L 5 228, CI 5 57, RI 5 80) resulting from analysis of the data matrix (as described in the text and in fig. 20), with the phylogenetic position of Anteucoila with the two representative figitids constrained.
Fig. 9 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 9. Photomicrograph of holotype male of Micropresbyteria caputipressa Liu and Engel, new genus and species (RTMP-96-9-170).
Fig. 5 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 5. Photomicrograph of holotype female of Proliopteron redactus Liu and Engel, new genus and species (CAS-409).
Fig. 13 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 13. Photomicrograph of holotype female of Jerseucoila plesiosoma Liu and Engel, new genus and species (NJ-1006).
Fig. 20 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 20. Strict consensus of 11 shortest trees (L 5 227, CI 5 56, RI 5 79) resulting from parsimony analysis of Ronquist's (1995b) data matrix, supplemented with paleontological data for several Late Cretaceous amber fossils described herein. We have added to the original matrix two additional characters (refer to section on Cladistics) and four fossil taxa (i.e., Protimaspis, Stolamissus, Anteucoila, and Proliopteron). No constraints were applied to the search which consisted of: hold 10,000; mult 5,000; wh*; max* in NONA (Goloboff, 1997). Values above branches are the number of unambiguous character changes supporting particular nodes, while those below are Jackknife and Bootstrap values.
Fig. 12 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 12. Holotype female of Anteucoila delicia Liu and Engel, new genus and species (RTMP-96-9-785); note that the right antenna (lower one in image) is partially pulled from the head capsule and so the basalmost sclerites depicted are not portions of the antenna but are instead sclerotic debris.
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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.