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Map 1 in A Generic-Level Revision Of The Spider Subfamily Coelotinae (Araneae, Amaurobiidae)
Map 1. Records of Ambanus.
Figs. 72, 73 in A Generic-Level Revision Of The Spider Subfamily Coelotinae (Araneae, Amaurobiidae)
Figs. 72, 73. Asiacoelotes xinhuiensis (Chen), male palp. 72. Ventral view. 73. Retrolateral view.
Figs. 57, 58. Ambanus mandzhuricus Ovtchinnikov, female. 57. Epigynum. 58 in A Generic-Level Revision Of The Spider Subfamily Coelotinae (Araneae, Amaurobiidae)
Figs. 57, 58. Ambanus mandzhuricus Ovtchinnikov, female. 57. Epigynum. 58. Vulva.
Map 2 in A Generic-Level Revision Of The Spider Subfamily Coelotinae (Araneae, Amaurobiidae)
Map 2. Records of Asiacoelotes.
Fig. 56. Preferred cladogram for 22 in A Generic-Level Revision Of The Spider Subfamily Coelotinae (Araneae, Amaurobiidae)
Fig. 56. Preferred cladogram for 22 genera. See text for discussion.
Figs. 38, 39 in A Generic-Level Revision Of The Spider Subfamily Coelotinae (Araneae, Amaurobiidae)
Figs. 38, 39. Coelotes atropos (Walckenaer), female. 38. Epigynum. 39. Vulva.
FIGURE 6 in Generic Concept Of The Phytoseiids (Acari: Phytoseiidae) According To Athias-Henriot
FIGURE 6: Some related characters considered for the definition of the genus Neoseiulus and of the species groups inside the genus, according to Athias-Henriot concept (after Ragusa and Athias-Henriot, 1983 modified).
FIGURE 2 in Generic Concept Of The Phytoseiids (Acari: Phytoseiidae) According To Athias-Henriot
FIGURE 2: (a) – Elaboration of Sellnick's and Garman's chaetotactic nomenclature system by Athias-Henriot (1957), using Blattisocius keegani Fox as example: (b) – Schematic position of dorsal setae for the phytoseiid genera Typhlodromus and Amblyseius; (after Athias- Henriot, 1957, 1958 modified).
FIGURE 5 in Generic Concept Of The Phytoseiids (Acari: Phytoseiidae) According To Athias-Henriot
FIGURE 5: Supraspecific grouping of Amblyseiini based on dorsal setal pattern and on the shape of the insemination apparatus (After Athias-Henriot, 1966 modified).
FIGURE 4 in Generic Concept Of The Phytoseiids (Acari: Phytoseiidae) According To Athias-Henriot
FIGURE 4: I – Dorsal chaetotactic nomenclature system adopted by Athias-Henriot for the Amblyseiini after Lindquist & Evans (1965). For more explanation see note 4. II – Position of the solenostome gv3 on ventrianal shield of the protoadenic gamasid Dendrolaelaps sp. (A), and of two phytoseiid mites: Dictydionotus desertus (B) and Cydnodromus fallacoides (C): a - pre-anal sigilla; b - peri-anal sigilla; V4 - para-anal setae (after Athias-Henriot, 1977 and 1978 modified).
FIGURE 3 in Generic Concept Of The Phytoseiids (Acari: Phytoseiidae) According To Athias-Henriot
FIGURE 3: Correspondances between Athias-Henriot's. (a) – and Hirschmann's; (b) – chaetotactic nomenclature systems. The drawing of Amblyseius leucophaeus Athias-Henriot 1959 is considered here as an example (after Athias-Henriot, 1957, 1959 modified).
Fig. 1. A in Cytotaxonomic diagnosis of Trichomycterus diabolus (Teleostei: Trichomycteridae) with comments about its evolutionary relationships with co-generic species
Fig. 1. A specimen of Trichomycterus diabolus with 110 mm in total length. Photo by C. Oliveira.
Figure 1 in Generic revision of the staphylinid beetle tribe Hoplandriini (Insecta: Coleoptera: Staphylinidae: Aleocharinae)
Figure 1. Single most-parsimonious cladogram of Hoplandriini modified from Hanley (2002a).
Perianth evolution and implications for generic delimitation in the Eucalypts (Myrtaceae): DNA sequences, morphological data
<p><em>Eucalyptus</em> was traditionally defined by the operculate perianth—hence the generic name (Latin, meaning "well-covered"). But after previous phylogenetic analysis placed <em>Angophora</em>, which has free sepals and petals, as sister to the bloodwood eucalypts, the latter were segregated into a new genus, <em>Corymbia</em>. We made a targeted capture of 101 low-copy nuclear exons from 392 samples representing 329 species-level taxa. The phylogeny was estimated using maximum likelihood (IQtree and RAxML) and the multi-species coalescent (Astral). We tested alternative relationships between four genera within Eucalypteae (<em>Arillastrum</em>, <em>Angophora</em>, <em>Eucalyptus</em>, <em>Corymbia</em>) at each of two nodes critical to generic delimitation using Shimodaira's Approximately Unbiased (AU) test. Monophyly of <em>Arillastrum</em> + (<em>Corymbia</em> + <em>Angophora</em>) relative to <em>Eucalyptus</em> sensu stricto was supported whereas monophyly of <em>Corymbia</em> relative to <em>Angophora</em> was decisively rejected. These results indicate that either <em>Eucalyptus</em> should be expanded to include all four genera or <em>Corymbia</em> should be split into two. All of the alternative relationships among the four currently recognised genera imply homoplasy in perianth evolution, specifically with respect to origins of the bud cap (operculum or calyptra), which has been traditionally used to define <em>Eucalyptus</em>. Inferred evolutionary transitions in perianth traits are generally congruent with divergences between major clades with a single exception: expression of separate sepals and petals in <em>Angophora</em>, which is nested within the operculate genus <em>Corymbia</em>, appears prima facie to be a reversal to the plesiomorphic perianth structure. Strictly, this is not a reversal because the petals of <em>Angophora</em> and <em>Corymbia</em> have a novel compound keel-and-limb structure that is absent in the outgroups. This structure is evident in early development, irrespective of whether the petals remain free or later become part of an operculum. Many of the currently recognised infrageneric taxa down to sectional level (and below in some cases) are well-supported by the sequence data and definable by morphological traits. Inclusion of <em>Angophora</em> within <em>Eucalyptus</em> was formally proposed two decades ago but did not gain acceptance. Here instead, we formally raise <em>Corymbia</em> subg. <em>Blakella</em> to genus rank and make the relevant new combinations.</p>
Search strategies for generic justification for a slot scanning, biplanar X-ray imaging system (EOS™ imaging system) for the diagnosis and assessment of orthopaedic conditions.
<p>The dataset includes the complete, reproducible search strategies for all literature databases searched during this project. The search strategies address the following research questions:</p> <p>RQ 1 To determine the test accuracy, clinical benefits and safety of slot scanning devices (EOS system) compared to conventional X-ray imaging for diagnosis of scoliosis and evaluation or monitoring of scoliosis patients.</p> <p>RQ 2 To determine the test accuracy, clinical benefits and safety of slot scanning devices (EOS system) compared to current practice for evaluation, monitoring or diagnosis of patients with other known or suspected orthopaedic conditions.</p>
Wide range of Brachyceran fly taxa attracted to synthetic and semi-synthetic generic noctuid lures and the description of new attractants for Sciomyzidae and Heleomyzidae families - RAW Data
<p>Wide range of Brachyceran fly taxa attracted to synthetic and semi-synthetic generic noctuid lures and the description of new attractants for Sciomyzidae and Heleomyzidae families - RAW Data </p>
FIG. 350–351. Proleg, left. 350 in Generic Revisions Of The Scopaeina And The Sphaeronina (Coleoptera: Staphylinidae: Paederinae: Lathrobiini)
FIG. 350–351. Proleg, left. 350. Sphaeronum sp. a. 351. Tripectenopus sp.
FIG. 403 in Generic Revisions Of The Scopaeina And The Sphaeronina (Coleoptera: Staphylinidae: Paederinae: Lathrobiini)
FIG. 403. Typhloleleupius nr. minutus. Head, ventral.
FIGS. 339–340. Trisunius spathulatus. 339. Labium, hypopharynx. 340 in Generic Revisions Of The Scopaeina And The Sphaeronina (Coleoptera: Staphylinidae: Paederinae: Lathrobiini)
FIGS. 339–340. Trisunius spathulatus. 339. Labium, hypopharynx. 340. Labrum, epipharynx.
FIGS. 256–258. Habitus. 256. Micranops brunneus, syntype. 257. Orus rubens. 258 in Generic Revisions Of The Scopaeina And The Sphaeronina (Coleoptera: Staphylinidae: Paederinae: Lathrobiini)
FIGS. 256–258. Habitus. 256. Micranops brunneus, syntype. 257. Orus rubens. 258. Trisunius sp.
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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.