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Figure 1. Phylogenetic relationships between Anthidiellum troodicum, A in Taxonomic status of the disjunct populations of the resin bee Anthidiellum breviusculum (Pérez, 1890) s.l. in the Mediterranean (Apoidea: Anthidiini)
Figure 1. Phylogenetic relationships between Anthidiellum troodicum, A. africanum sp. nov. and A. breviusculum as inferred from COI (mitochondrial cytochrome c oxidase I) DNA sequences. The phylogram shows the best-scoring maximum likelihood tree. Numbers shown at nodes are maximum likelihood bootstrap values based on 1000 bootstrap replicates. A set of 36 COI sequences of Anthidiellum strigatum from different parts of its distribution range was used as outgroup.
FIGURE 10 in Phylogenetic relationships, host associations, and three new species of a poorly known group of "tetraphyllidean" tapeworms from elasmobranchs
FIGURE 10. Scanning electron micrographs of Zyxibothrium healyae n. sp. (A) Scolex, small letters indicate location of details in micrographs B–G. (B) Apex of scolex sparsely covered with long slender aristate gladiate spinitriches and densely packed capilliform filitriches. (C) Proximal surface of anterior loculus densely covered with long slender aristate gladiate spinitriches interspersed with gladiate spinitriches, filitriches not observed. (D) Proximal surface of middle loculus densely covered with long slender aristate gladiate spinitriches interspersed with gladiate spinitriches, filitriches not observed. (E) Proximal surface of posterior loculus densely covered with long slender gladiate spinitriches, filitriches not observed. (F) Distal bothridial surface densely covered with long slender aristate gladiate spinitriches interspersed with capilliform filitriches. (G) Cephalic peduncle densely covered with large gladiate spinitriches interspersed with small gladiate spinitriches, filitriches not observed.
FIGURE 9 in Phylogenetic relationships, host associations, and three new species of a poorly known group of "tetraphyllidean" tapeworms from elasmobranchs
FIGURE 9. Line drawings of Zyxibothrium healyae n. sp. (A) Scolex (paratype, CR-76-1, NMNZ No. W.003931). (B) Detail of terminal genitalia (holotype, CR-75-2, NMNZ No. W.003930). (C) Whole worm (holotype, CR-75-2, NMNZ No. W.003930). (D) Mature proglottid (paratype, CR-75-1, LRP No. 9799).
FIGURE 6 in Phylogenetic relationships, host associations, and three new species of a poorly known group of "tetraphyllidean" tapeworms from elasmobranchs
FIGURE 6. Scanning electron micrographs of Zyxibothrium kamienae Hayden and Campbell 1981. (A) Scolex, small letters indicate location of details in micrographs B–H. (B) Apex of scolex densely covered with very long slender aristate gladiate spinitriches interspersed with gladiate spinitriches, filitriches not observed. (C) Distal bothridial surface densely covered with very long slender aristate gladiate spinitriches interspersed with gladiate spinitriches, filitriches not observed. (D) Posterior region of scolex proper densely covered with gladiate spinitriches, filitriches not observed. (E) Proximal bothridial surface away from locular margins densely covered with gladiate spinitriches, filitriches not observed. (F) Proximal surface of anterior loculus densely covered with very long slender aristate gladiate spinitriches interspersed with gladiate spinitriches, filitriches not observed. (G) Proximal surface of paired loculi densely covered with very long slender aristate gladiate spinitriches interspersed with gladiate spinitriches, filitriches not observed. (H) Proximal surface of posterior loculus densely covered with long slender gladiate spinitriches interspersed with acicular filitriches.
FIGURE 3 in Phylogenetic relationships, host associations, and three new species of a poorly known group of "tetraphyllidean" tapeworms from elasmobranchs
FIGURE 3. Line drawings of Pentaloculum grahami n. sp. (A) Scolex (paratype, SA-2-1, LRP No. 10947). (B) Mature subterminal proglottid (paratype, SA-16-1, USNM No. 1678892). (C) Detail of terminal genitalia (holotype, SA-16-3, QM No. G240343). (D) Gravid terminal proglottid (holotype, SA-16-3, QM No. G240343). (E) Whole worm (holotype, SA-16-3, QM No. G240343).
FIGURE 5 in Phylogenetic relationships, host associations, and three new species of a poorly known group of "tetraphyllidean" tapeworms from elasmobranchs
FIGURE 5. Photomicrographs of cocoons of Pentaloculum grahami n. sp. showing variation in number of oncospheres. (A) Cocoon containing five oncospheres. (B) Cocoon containing six oncospheres.
FIGURE 1 in Phylogenetic relationships, host associations, and three new species of a poorly known group of "tetraphyllidean" tapeworms from elasmobranchs
FIGURE 1. Phylogenetic tree resulting from Bayesian Inference and Maximum Likelihood analyses of the D1–D3 region of the 28S rDNA gene for species in Clade 1 of Caira et al. (2017) (green box). Scale bar indicates substitutions per site. Nodes with bootstrap values ≥ 90 and posterior probabilities ≥ 99 are indicated by black dots. Nodes with bootstrap values ≥ 70 and posterior probabilities ≥ 95 are indicated by grey dots. Taxon labels are presented as cestode and host names followed by host specimen number in parentheses, Lawrence R. Penner Parasitological Collection accession number for hologenophores, and GenBank accession number. Newly generated sequences are in boldface type.
FIGURE 2 in Phylogenetic relationships, host associations, and three new species of a poorly known group of "tetraphyllidean" tapeworms from elasmobranchs
FIGURE 2. Scanning electron micrographs of Pentaloculum macrocephalum Alexander 1963. (A) Scolex, small letters indicate location of details in micrographs B–F. (B) Distal bothridial surface densely covered with long-tipped aristate gladiate spinitriches interspersed with gladiate spinitriches and capilliform filitriches. (C) Cephalic peduncle densely covered with large gladiate spinitriches, filitriches not observed. (D) Proximal surface of anteriormost loculus densely covered with longtipped aristate gladiate spinitriches interspersed with gladiate spinitriches and capilliform filitriches. (E) Proximal surfaces of anterior pair of loculi densely covered with long-tipped aristate gladiate spinitriches interspersed with gladiate spinitriches and capilliform filitriches. (F) Proximal surfaces of posterior pair of loculi densely covered with long-tipped aristate gladiate spinitriches interspersed with gladiate spinitriches and capilliform filitriches.
FIGURE 8 in Phylogenetic relationships, host associations, and three new species of a poorly known group of "tetraphyllidean" tapeworms from elasmobranchs
FIGURE 8. Scanning electron micrographs of Zyxibothrium duffyi n. sp. (A) Scolex, small letters indicate location of details in micrographs B–G. (B) Apex of scolex densely covered with capilliform filitriches. (C) Proximal surface of anteriormost loculus densely covered with long slender aristate gladiate spinitriches interspersed with gladiate spinitriches and capilliform filitriches. (D) Proximal surfaces of anterior pair of loculi densely covered with long slender aristate gladiate spinitriches interspersed with gladiate spinitriches and capilliform filitriches. (E) Proximal surfaces of posterior pair of loculi densely covered with long slender aristate gladiate spinitriches interspersed with gladiate spinitriches, filitriches not observed. (F) Distal bothridial surface densely covered with long slender aristate gladiate spinitriches interspersed with gladiate spinitriches and capilliform filitriches. (G) Cephalic peduncle densely covered with long slender gladiate spinitriches interspersed with long slender aristate gladiate spinitriches, filitriches not observed.
FIGURE 4 in Phylogenetic relationships, host associations, and three new species of a poorly known group of "tetraphyllidean" tapeworms from elasmobranchs
FIGURE 4. Scanning electron micrographs of Pentaloculum grahami n. sp. (A) Scolex, small letters indicate location of details in micrographs B–H. (B) Distal bothridial surface densely covered with long-tipped aristate gladiate spinitriches interspersed with gladiate spinitriches and capilliform filitriches. (C) Apex of scolex covered with gladiate spinitriches and densely packed capilliform filitriches. (D) Scolex proper densely covered with gladiate spinitriches interspersed with capilliform filitriches. (E) Proximal surface of margin of anteriormost loculus densely covered with long-tipped aristate gladiate spinitriches interspersed with gladiate spinitriches and capilliform filitriches. (F) Proximal surfaces of margins of anterior pair of loculi densely covered with long-tipped aristate gladiate spinitriches interspersed with gladiate spinitriches and capilliform filitriches. (G) Proximal surfaces of margins of posterior pair of loculi densely covered with long-tipped aristate gladiate spinitriches interspersed with gladiate spinitriches and capilliform filitriches. (H) Proximal surfaces away from margins of posterior pair of loculi densely covered with short-tipped wide aristate gladiate spinitriches, filitriches not observed.
FIGURE 3. Frullania iriomotensis S.Hatt. A in Range extension, taxonomic note, molecular-phylogenetic relationship, and conservation of Frullania iriomotensis S.Hatt. (Marchantiophyta, Frullaniaceae), a rare liverwort previously known only from the type locality in Japan
FIGURE 3. Frullania iriomotensis S.Hatt. A. Portion of plant with gynoecium and androecium, ventral view. B. Portion of plant with gynoecium, ventral view. C. Perianth. D–E. Innermost female bracts. F. Innermost female bracteole. G. Surface of perianth. H–I. Portions of perianth beak with single-celled protuberances. J. Transverse sections of perianth. L. Portion of plant with androecium, ventral view. M. Portion of plant, ventral view. A–J. from R.L. Zhu et al. 20210126–101B (HSNU), L–M. from M. Mizutani & I. Yoshimura 5506/a (holotype: NICH).
FIGURE 2. Frullania iriomotensis S.Hatt. A–C in Range extension, taxonomic note, molecular-phylogenetic relationship, and conservation of Frullania iriomotensis S.Hatt. (Marchantiophyta, Frullaniaceae), a rare liverwort previously known only from the type locality in Japan
FIGURE 2. Frullania iriomotensis S.Hatt. A–C. Portions of plant, A. dorsal view, B–C. ventral views. D. Lateral leaf. E. Underleaf. F. Leaf lobule. G. Stylus. H. Initial lobe of branch. I. Leaf lobe cells, showing oil bodies. J. Transverse section of stem. A–B., H–I. from R.L. Zhu et al. 20210126–102 (HSNU). C–G., J. from R.L. Zhu et al. 20210126–101B (HSNU).
FIGURE 1 in Range extension, taxonomic note, molecular-phylogenetic relationship, and conservation of Frullania iriomotensis S.Hatt. (Marchantiophyta, Frullaniaceae), a rare liverwort previously known only from the type locality in Japan
FIGURE 1. Majority-rule consensus tree based on Bayesian analyses of the combined dataset of nrITS–2, rbcL and trnL–F. Bayesian posterior probabilities values (BI–PP) and ML bootstrap values (ML–BS), are indicated at branches (BI–PP/ML–BS).
Figure 17 in The fifth family of the true crickets (Insecta: Orthoptera: Ensifera: Grylloidea), Oecanthidae defin. nov.: phylogenetic relationships and divergence times
Figure 17. Angustitrella sp., male: A, dorsal habitus; B, right FW. C, Paroecanhtus aztecus, male genitalia, dorsal view. Scales: 1 mm. Abbreviations: see Material and methods.
Figure 11. A in The fifth family of the true crickets (Insecta: Orthoptera: Ensifera: Grylloidea), Oecanthidae defin. nov.: phylogenetic relationships and divergence times
Figure 11. A, Cearacesa sp., frontal head; B, A. (Aphonomorphus) aff. montanus, maxillary palpus. Scale: 1mm.
Figure 10. A in The fifth family of the true crickets (Insecta: Orthoptera: Ensifera: Grylloidea), Oecanthidae defin. nov.: phylogenetic relationships and divergence times
Figure 10. A, Fryerius sp., male, dorsal habitus; B, Munda aff. asyrinx, male, dorsal habitus; C, Truljalia hibinonis, male, pronotum and FW, dorsal view; D, Madasumma melanotum, male genitalia, lateral view. Scales: 1mm. Abbreviations: see Material and methods.
Figure 7 in The fifth family of the true crickets (Insecta: Orthoptera: Ensifera: Grylloidea), Oecanthidae defin. nov.: phylogenetic relationships and divergence times
Figure 7. Neoxabea breƲipes. A, hind tibia and tarsi; B, hind tibia distal margin and tarsi, inner view; C, hind tibia distal margin and tarsi, outer view. Scales: 1mm. Abbreviations: see Material and methods.
Figure 18. A in The fifth family of the true crickets (Insecta: Orthoptera: Ensifera: Grylloidea), Oecanthidae defin. nov.: phylogenetic relationships and divergence times
Figure 18. A, Brazitrypa paulista, male; B, Cylindrogryllus pitanga, male, FWs and metanotum; C, Neometrypus badius, male genitalia, ventral view. Scales: 1 mm. Abbreviations: see Material and methods.
Figure 5. A in The fifth family of the true crickets (Insecta: Orthoptera: Ensifera: Grylloidea), Oecanthidae defin. nov.: phylogenetic relationships and divergence times
Figure 5. A, Euscyrtus aff. bipunctatus, male, dorsal habitus. Proturana subapterus: B, head and pronotum, lateral view; C, claw; D, ovipositor; dorsal view. Scales: 1mm.
Figure 14. A, H in The fifth family of the true crickets (Insecta: Orthoptera: Ensifera: Grylloidea), Oecanthidae defin. nov.: phylogenetic relationships and divergence times
Figure 14. A, H. (Hapithus) Ʋagus, male, dorsal habitus; B, Stenogryllus sp., male, pronotum and FW, dorsal view; C, H. (Hapithus) sp., male genitalia, lateral view. Scales: 1mm. Abbreviations: see Material and methods.
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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.