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Fig. 3. Cladogram for the combined 16S in On ''Molecular Phylogeny of Vespidae (Hymenoptera) and the Evolution of Sociality in Wasps''
Fig. 3. Cladogram for the combined 16S data and the morphological and behavioral characters (see appendix 1). The length is 652 steps; consistency index = 0.64 and retention index = 0.69.
Fig. 4. Consensus tree for the combined 28S in On ''Molecular Phylogeny of Vespidae (Hymenoptera) and the Evolution of Sociality in Wasps''
Fig. 4. Consensus tree for the combined 28S data and the morphological and behavioral characters (see appendix 1). The length is of the two underlying cladograms is 458 steps; consistency index = 0.81 and retention index = 0.85.
Fig. 5 in On ''Molecular Phylogeny of Vespidae (Hymenoptera) and the Evolution of Sociality in Wasps''
Fig. 5. Cladogram for the combined sequence datasets and the morphological and behavioral characters. The length is 907 steps; consistency index = 0.68 and retention index = 0.75.
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.
Fig. 11 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 11. Photomicrograph of holotype female of Anteucoila delicia Liu and Engel, new genus and species (RTMP-96-9-785).
Fig. 17 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 17. Photomicrograph of holotype male of Tanaoknemus ecarinatus Liu and Engel, new genus and species (CAS-78).
Fig. 7 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 7. Photomicrograph of holotype female of Goerania petiolata Liu and Engel, new genus and species (CAS).
Fig. 3 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 3. Photomicrograph of holotype female of Stolamissus mirabilis Liu and Engel, new genus and species (NJ-709).
Fig. 15 in Phylogeny and Geological History of the Cynipoid Wasps (Hymenoptera: Cynipoidea)
Fig. 15. Photomicrograph of holotype female of Syneucoila magnifica Liu and Engel, new genus and species (NJ-1075).
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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)
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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.