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Figs 10–19. 10–11 in Braconidae (Hymenoptera) From Korea, Xxiv. Species Of Thirteen Subfamilies
Figs 10–19. 10–11: Bracon (Ophthalmobracon) acunens sp. n.: first tergite (m paratype). – 12– 16. Bracon (Ophthalmobacon) ophthalmicus Telenga (12–13, 15–16: f paratype; 14: m paratype): 12 = head in dorsal view, 13 = tergites 1–3, 14 = tergite 1, 15 = distal part of right fore wing, 16 = hind femur. – 17–19. Bracon (Sculptobracon) yakui Watanabe (f): 17 = head in lateral view, 18 = head in dorsal view, 19 = distal part of right fore wing
Figs 40–51. 40–41 in Braconidae (Hymenoptera) From Korea, Xxiv. Species Of Thirteen Subfamilies
Figs 40–51. 40–41. Aleiodes (Aleiodes) subcompressus sp. n. (f holotype): 40 = distal part of right fore wing, 41 = ultimate three flagellomeres. – 42–45. Aleiodes (Aleiodes) pallidator (Thunberg) (f): 42 = tergites 1–2, 43 = head in dorsal view, 44 = hind femur, 45 = ultimate three flagellomeres. – 46–47. Blacus (Leioblacus) fischeri Haeselbarth (f): 46 = propodeum, 47 = distal part of right fore wing. – 48. Chelonus moczari sp. n. (f holotype): posterior half of carapace in ventral view. – 49. Chelonus asiaticus Telenga (fm): distal part of right fore wing. – 50. Chelonus formosanus Sonan (f): distal part of right fore wing. – 51. Microchelonus koreanus Tobias (m): apical foramen of carapace
Figs 30–39. – 30 in Braconidae (Hymenoptera) From Korea, Xxiv. Species Of Thirteen Subfamilies
Figs 30–39. – 30 = Bracon (Glabrobracon) claripennis Thomson (f): distal part of right fore wing. – 31–34. Aleiodes (Aleiodes) subcompressus sp. n. (f holotype): 31 = head in dorsal view, 32 = head in lateral view, 33 = hind femur, 34 = tergites 1–3. – 35–38. Aleiodes (Aleiodes) angustatus (Papp) (f holotype): 35 = tergites 1–3, 36 = hind femur, 37 = head in lateral view, 38 = head in dorsal view. – 39. Aleiodes (Aleiodes) pallidator (Thunberg) (f): head in lateral view
Fig. 3 in A New Species of the Subfamily Coelotinae (Araneae: Agelenidae) from Shiga and Fukui Prefectures, Japan
Fig. 3. Comparison of the male palp of three species inhabiting around Lake Biwa. Coelotes nojimai sp. nov. [1 paratype, NSMT-Ar 20962– 6], C. nagaraensis [7 (topotype)–12], and C. yodoensis [13 (topotype)–18]. The photo numbers correspond to the numbers indicating the collection localities on the map. Scale bars: 0.5 mm.
Fig. 5 in A New Species of the Subfamily Coelotinae (Araneae: Agelenidae) from Shiga and Fukui Prefectures, Japan
Fig. 5. Distribution of Coelotes nojimai sp. nov. and two closely related species, C. nagaraensis and C. yodoensis, on Honshu Island, Japan.
Figure 3 Nycteridocaulus sulcatussp. n in Two new feather mites of the subfamily Proctophyllodinae (Acariformes: Proctophyllodidae) from the Yellow-bellied Flycatcher Empidonax flaviventris (Passeriformes: Tyrannidae) in Canada
Figure 3 Nycteridocaulus sulcatussp. n., details: A–C – legs I–III of male, respectively, D – tibia and tarsus IV of male, E – tibia and tarsus IV of female, F – spermatheca and spermaducts, G – opisthosoma of male, ventral view. Abbreviations: ad– adanal shield, ga– genital arch, hs– head of spermatheca, pd– primary spermaduct, pg – pregenital apodemes, sd – secondary spermaducts, tl– terminal lamella.
Figure 2 in A comprehensive molecular phylogeny of Geometridae (Lepidoptera) with a focus on enigmatic small subfamilies
Figure 2 Evolutionary relationships of the subfamily Sterrhinae. Numbers above branches are SH-aLRT support (%)/ultrafast bootstrap support, UFBoot2(%), for nodes to the right of the numbers. Values of SH ≥ 80 and UFBoot2 ≥ 95 indicate well-supported clades (Trifinopoulos & Minh, 2018). * FormaltaxonomictreatmentwillbedealtwithinP. Sihvonenetal., 2019, unpublisheddata. Full-size DOI: 10.7717/peerj.7386/fig-2
Figure 1 in A comprehensive molecular phylogeny of Geometridae (Lepidoptera) with a focus on enigmatic small subfamilies
Figure 1 Evolutionary relationships of major groups of the family Geometridae. Numbers above branches are SH-aLRT support (%)/ultrafast bootstrap support, UFBoot2(%), for nodes to the right of the numbers. Values of SH ≥ 80 and UFBoot2 ≥ 95 indicate well-supported clades (Trifinopoulos & Minh, 2018). *FormaltaxonomictreatmentwillbedealtwithinP. Sihvonenetal., 2019, unpublisheddata. § Epidesmiinae subfam. nov. See Oenochrominae section for more details. Full-size DOI: 10.7717/peerj.7386/fig-1
Figure 5 in A comprehensive molecular phylogeny of Geometridae (Lepidoptera) with a focus on enigmatic small subfamilies
Figure 5 Evolutionary relationships of the subfamily Geometrinae. Numbers above branches are SH-aLRT support (%)/ultrafast bootstrap support, UFBoot2(%), for nodes to the right of the numbers. Values of SH ≥ 80 and UFBoot2 ≥ 95 indicate well-supported clades (Trifinopoulos & Minh, 2018). Taxonomicchangesareindicatedbyasymobolizedarrow>. § Newsubfamily. Full-size DOI: 10.7717/peerj.7386/fig-5
Figure 3 in A comprehensive molecular phylogeny of Geometridae (Lepidoptera) with a focus on enigmatic small subfamilies
Figure 3 Evolutionary relationships of the subfamily Larentiinae. Numbers above branches are SH-aLRT support (%)/ultrafast bootstrap support, UFBoot2(%), for nodes to the right of the numbers. Values of SH ≥ 80 and UFBoot2 ≥ 95 indicate well-supported clades (Trifinopoulos & Minh, 2018). * FormaltaxonomictreatmentwillbedealtwithinP. Sihvonenetal., 2019, unpublisheddata. Full-size DOI: 10.7717/peerj.7386/fig-3
Figure 4 in A comprehensive molecular phylogeny of Geometridae (Lepidoptera) with a focus on enigmatic small subfamilies
Figure 4 Phylogenetic relationships of the subfamilies Archierinae, Desmobathrinae, Epidesmiinae subfam. nov., Oenochrominae. Numbers above branches are SH-aLRT support (%)/ultrafast bootstrap support, UFBoot2(%), for nodes to the right of the numbers. Values of SH ≥ 80 and UFBoot2 ≥ 95 indicatewell-supportedclades (Trifinopoulos & Minh, 2018). Taxonomicchangesareindicatedbyasymobolizedarrow>. * Formal taxonomic treatment will be dealt with in P. Sihvonen et al., 2019, unpublished data. Full-size DOI: 10.7717/peerj.7386/fig-4
Comparative genomics of eight aphid subfamilies reveals variable relationships between host horizontally-transferred genes and symbiont peptidoglycan metabolism.
<p>Genome assemblies, annotations, and orthologs of aphids (<em>Geopemphigus sp.</em>, <em>Stegophylla sp.</em>, <em>Chaitophorus viminalis</em>, and<em> Pemphigus obesinymphae</em>) and their symbionts. </p> <p>step1_final_assemblies_and_annotations.tar.gz: Aphid genomes and annotations</p> <p>step2_protein_evidence_used_for_genome_annotation.tar.gz: Protein evidence used for aphid genome annotation</p> <p>step3_amino_acid_inputs_for_aphid_orthologs: amino acid inputs for aphid ortholog assignmentt</p> <p>step5_buchnera_genomes_and_annotations.tar.gz: Buchnera genomes and annotations</p>
Fig. 11 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus
Fig. 11. Lateral view of propodeum, showing: A) Propodeal spiracle separated from declivity margin by a distance longer than its diameter (Typhlomyrmex lavra); B) Propodeal spiracle close to the declivous face of propodeum (Holcoponera relicta—USNMENT00412058). Photos by Gabriela Camacho (A) and Jeffrey Sosa-Calvo; available from www.antweb.org (Antweb 2021).
Fig. 10 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus
Fig. 10. Lateral view of gaster, showing: A) Second gastric segment (IV abdominal) relatively straight (Gnamptogenys acuminata—USNMENT00441095); B) Second gastric segment (IV abdominal) slightly arched ventrally (Poneracantha mecotyle—CASENT0281530). Photos by Jeffrey Sosa-Calvo (A) and Zach Lieberman (B); available from www.antweb.org (Antweb 2021).
Fig. 8 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus
Fig. 8. Lateral view of gaster, showing: A) Second gastral (IV abdominal) sternite not strongly reduced in relation to the tergite; dorsal profile of gaster gently convex, so that the apex of gaster is only discretely directed ventrally (Gnamptogenys acuminata—USNMENT00441095); B) Second gastral (IV abdominal) sternite strongly reduced in relation to the tergite; dorsal profile of gaster extremely convex, so that the gaster is strongly directed ventrally and anterad (Alfaria minuta—CASENT0281213). Photos by Jeffrey Sosa-Calvo (A) and Estella Ortega (B); available from www.antweb.org (Antweb 2021).
Fig. 5 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus
Fig. 5. Lateral view of pronotum, showing: A) Pronotal tubercles present; mesonotum prominent, separated from propodeum by a deep transversal suture (Ectatomma tuberculatum—CASENT0173380); B) Pronotal tubercles or projections absent; mesonotum not prominent, forming a continuous profile with propodeum (Holcoponera striatula—CASENT0173386). Photos by April Nobile; available from www.antweb.org (Antweb 2021).
Fig. 7 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus
Fig. 7. Frontal view of head, showing: A) Expanded frontal lobes (Alfaria falcifera—CASENT0179971); B) Occipital lobes absent (Gnamptogenys continua— CASENT0173383). Photos by Erin Prado (A) and April Nobile (B); available from www.antweb.org (Antweb 2021).
Fig. 1 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus
Fig. 1. In lateral view, workers of the Ectatomminae genera, showing the morphological diversity within the clade. (A) Acanthoponera mucronata (CASENT0173540), (B) Alfaria minuta (CASENT0281213), (C) Ectatomma planidens (CASENT0173379), (D) Gnamptogenys acuminata (USNMENT00441095), (E) Heteroponera panamensis (CASENT0106021), (F) Holcoponera ammophila (CASENT0281512), (G) Poneracantha mecotyle (CASENT0281530), (H) Rhytidoponera metallica (CASENT0172345), (I) Stictoponera biroi (CASENT0172380), (J) Typhlomyrmex rogenhoferi (CASENT0173390). See Fig. 3 for images of Boltonia microps. Images by April Nobile, Estella Ortega, Michael Branstetter, Zach Lieberman, and Jeffrey Sosa-Calvo; available from www.antweb.org (Antweb 2021).
Fig. 3 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus
Fig. 3. Worker of Boltonia microps in A) frontal view; B) dorsal view; and C) lateral view. Images by April Nobile (CASENT0173544); available from www.antweb. org (Antweb 2021).
Fig. 2 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus
Fig. 2. Phylogeny of the subfamily Ectatomminae based on phylogenomic analyses of the UCE 90% complete data set (150 taxa). Figure is based on IQ-Tree besttree searches with ultrafast bootstrap (UFB) frequencies of less than 100% mapped onto the respective nodes. UFB searches consisted of 1000 replicates.The eleven larger ectatommine lineages are indicated. Branch color indicates the biogeographical range of the species.Taxa marked with asterisk (*) were classified in Gnamptogenys prior to this revision and those with double asterisk (**) were included in Heteroponera prior to this revision. See Supplementary material for the 75% complete matrix (Supp Fig. S1 [online only]). Ant photos show heads in frontal view of, from top to bottom:Gnamptogenys acuminata (USNMENT00441095), Typhlomyrmex rogenhoferi (CASENT0004700), Holcoponera striatula (CASENT0106042), Alfaria simulans (CASENT0603729), Poneracantha rastrata (CASENT0281223), Stictoponera biroi (CASENT0281519), Rythidoponera metallica (CASENT0172345), Ectatomma lugens (USNMENT00445341), Heteroponera brounii (CASENT0172105), Acanthoponera mucronata (CASENT0173540), and Boltonia microps (CASENT0173544). Images by April Nobile, Jeffrey Sosa-Calvo, Zach Lieberman,Will Ericson, Michael Branstetter, and Estella Ortega; available from www.antweb.org (Antweb 2021).
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.