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Figure 6. A in Classical taxonomy, molecular phylogeny and genetic analysis of the genus Exitianus Ball, 1929 (Hemiptera: Cicadellidae: Deltocephalinae) from Egypt
Figure 6. A. Amino acids variations of the COX1 gene generated by WebLogo3 server. B. Multiple amino acids alignments for selected Exitianus isolates generated by MultAlin server.
Figure 2. Exitianus nanus. A in Classical taxonomy, molecular phylogeny and genetic analysis of the genus Exitianus Ball, 1929 (Hemiptera: Cicadellidae: Deltocephalinae) from Egypt
Figure 2. Exitianus nanus. A. Habitus, dorsal view; B. Habitus, female ventral view; C. Habitus, male ventral view; D. Pronotum & scutellum; E. Face; F. Male genitalia (pygofer, subgenital plate, valva, styles and connective, aedeagus).
Figure 1. Exitianus capicola. A in Classical taxonomy, molecular phylogeny and genetic analysis of the genus Exitianus Ball, 1929 (Hemiptera: Cicadellidae: Deltocephalinae) from Egypt
Figure 1. Exitianus capicola. A. Habitus, dorsal view; B. Habitus, female ventral view; C. Habitus, male ventral view; D. Pronotum
Figure 3. Exitianus pondus. A in Classical taxonomy, molecular phylogeny and genetic analysis of the genus Exitianus Ball, 1929 (Hemiptera: Cicadellidae: Deltocephalinae) from Egypt
Figure 3. Exitianus pondus. A. Habitus, dorsal view; B. Habitus, female ventral view; C. Habitus, male ventral view; D. Pronotum & scutellum; E. Face; F. Male genitalia (pygofer, subgenital plate, valva, styles and connective, aedeagus); G. Aedeagus, lateral view.
Figure 1 in Integrative taxonomy, distribution, and host associations of Geocenamus brevidens and Quinisulcius capitatus from southern Alberta, Canada
Figure 1: Light photomicrographs of Geocenamus brevidens. (A) Entire female, (B) Esophageal region, (C) Lip region, (D) Posterior esophageal region, (E) Deirids, (F) Posterior region with complete reproductive system, (G) Lateral lines, (H-J) Vulval region, (K-O) Female tails. Scale bars: (A) 50 μm; (B-D, E, H-O) 20 μm, (F) 50 μm, (G) 5 μm. Arrows point to (a) anus, (d) deirids, (exp) excretory pore, (ph) phamsid, and (v) vulva.
Figure 4 in Integrative taxonomy, distribution, and host associations of Geocenamus brevidens and Quinisulcius capitatus from southern Alberta, Canada
Figure 4: Phylogenetic relationships within selected genera of subfamily Telotylenchinae and subfamily Merliniinae as inferred from Bayesian analysis using the 28S of the rRNA gene sequence dataset with the GTR + I + G model (lnL = 6,015.1425; AIC = 12,526.2851; freq A = 0.1987; freq C = 0.2072; freq G = 0.3206; freq T = 0.2736; R(a) = 0.4322; R(b) = 2.5823; R(c) = 1.2662; R(d) = 0.2497; R(e) = 5.4146; R(f) = 1.0000). Posterior probability of more than 70% is given for appropriate clades. Newly obtained sequences are indicated in bold.
Figure 3 in Integrative taxonomy, distribution, and host associations of Geocenamus brevidens and Quinisulcius capitatus from southern Alberta, Canada
Figure 3: Phylogenetic relationships within selected genera of subfamily Telotylenchinae and subfamily Merliniinae as inferred from Bayesian analysis using the 18S of the rRNA gene sequence dataset with the GTR + I + G model (lnL = 1,910.5101; AIC = 4,017.0201; freq A = 0.2500; freq C = 0.2500; freq G = 0.2500; freq T = 0.2500; R(a) = 1.0000; R(b) = 3.9248; R(c) = 1.0000; R(d) = 1.0000; R(e) = 4.6930; R(f) = 1.0000). Posterior probability of more than 70% is given for appropriate clades. Newly obtained sequences are indicated in bold. *** need to be revised by integrative taxonomy.
Figure 36 in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 36. Images of live female argonauts, Argonauta hians and A. nodosus, demonstrating the effect of spawned eggs on the position of the females relative to their shells: a, live female A. hians from Andaman Sea, Thailand, photographed in an aquarium (photo: J. Nabhitabhata, after Sukhsangchan and Nabhitabhata 2007); b–c, A. nodosus Phillip Bay, Victoria, Australia (photos: R. Kuiter); b, live female argonaut photographed in the wild; c, eggs of same specimen, shown with argonaut removed from shell.
Figure 35. Preserved female Argonauta nouryi and A in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 35. Preserved female Argonauta nouryi and A. hians with spawned eggs: a, preserved female A. nouryi from the Pacific Ocean (15.2 mm dorsal mantel length, 18.4 mm shell length, SBMNH 64369) with spawned eggs attached to the axis of the shell; b, preserved female A. hians from the North West Shelf, Western Australia (28.7 mm dorsal mantel length, 38.9 mm shell length, QM Mo77789) with yellow eggs visible in dorsal component of shell. Scale bar = 1 cm.
Figure 33. Repaired Argonauta argo shell from Monterey, California. Repaired A in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 33. Repaired Argonauta argo shell from Monterey, California. Repaired A. argo shell from Monterey, California (81.9 mm shell length, USNM 61374): a, left lateral view; b, oblique left lateral view; c, oblique anterior aperture view. Note change in direction of lateral ribs along repair line. Scale bar = 1 cm.
Figure 32 in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 32. Coarse and fine Argonauta argo shells: a–b, shells of A. argo displaying different degree of sculpturing and variation in the aperture edge; a, fine A. argo shell from off San Clement Island, California (113.3 mm shell length [P], USNM 316580); b, coarse A. argo shell from Baja California (128.1 mm shell length [P], ANSP 404279). Scale bar = 1 cm.
Figure 31 in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 31. Single eared Argonauta nodosus shell from the British Museum: a–c, three perspectives of a single eared A. nodosus shell from the British Museum (109.0 mm shell length [P], BMNH unreg., locality unknown, "B395, e."); a, left lateral view; b, right lateral view; c, anterior aperture view. Scale bar = 1 cm.
Figure 29 in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 29. Coarse and fine Argonauta nodosus shells: a, fine A. nodosus shell from Mayor Is., Bay of Plenty, New Zealand (127.2 mm shell length, NMV F164784); b, Coarse A. nodosus shell from the Indo Pacific (127.3 mm shell length, NMV F164774). Scale bar = 1 cm.
Figure 27 in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 27. Shell consistent with description of Argonauta boettgeri from Museums Victoria: a–d, four perspectives of a shell consistent with A. boettgeri (treated here as a synonym of A. hians [Lightfoot], 1786) from Museums Victoria (25.0 mm shell length, NMV F164767) displaying an increase in keel tubercle size consistent with a shift from Type 2 shell formation (T2) to Type 1 shell formation (T1); a, left lateral view; b, right lateral view; c, anterior aperture view; d, posterior keel view. Scale bar = 1 cm.
Figure 28 in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 28. Reproduced illustrations referenced in the descriptions of Argonauta nodosus [Lightfoot], 1786 and A. argo Linnaeus, 1758: a, illustration of A. nodosus [Lightfoot], 1786, designated as a lectotype by Moolenbeek (2008), Rumphius 1705, pl. 18, fig. 1; b, illustration of A. argo Linnaeus, 1758, considered a paralectotype following the designation of a lectotype by Moolenbeek (2008), Rumphius 1705, pl. 18, fig. A.
Figure 34 in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 34. Single eared Argonauta argo shell from Venezuela, South America: a–c, three perspectives of a single eared A. argo shell from Venezuela (51.4 mm shell length, USNM 122208); a, left lateral view; b, right lateral view; c, anterior aperture view. Scale bar = 1 cm.
Figure 26 in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 26. Argonauta hians shell from the British Museum: a–d, four perspectives of an A. hians shell from the British Museum (76.1 mm shell length [P], BMNH unreg., locality unknown, "B698, t.") which, while displaying an aperture shape and axial region consistent with the original description of A. boettgeri (fig. 22B, C), shows signs of possessing ears (E) at an earlier stage of growth; a, left lateral view; b, right lateral view; c, anterior aperture view; d, posterior keel view. A shift from Type 1 shell formation (T1) to Type 2 shell formation (T2) is expressed by ears subsumed and a reduction in keel tubercle size on the right side only. Scale bar = 1 cm.
Figure 25 in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 25. Single eared Argonauta hians shell from Madagascar: a–c, three perspectives of a single eared A. hians shell from Madagascar (60.8 mm shell length, NMV F164734); a, left lateral view; b, right lateral view; c, anterior aperture view. Scale bar = 1 cm.
Figure 24 in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 24. Argonauta hians shell from the North West Shelf, Western Australia: a–d, four perspectives of an A. hians shell from the North West Shelf, Western Australia (53.0 mm shell length, WAM S31510) displaying a clear shift from Type 1 shell formation (T1) to Type 2 formation (T2) indicated by a reduction in the size and spacing of the keel tubercles and a reduction in the ratio of ribs to keel tubercles (from approximately 1.5:1 to 1:1); a, right lateral view; b, oblique right lateral view; c, anterior aperture view; d, posterior keel view. Scale bar = 1 cm.
Figure 23 in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 23. Argonauta hians shell from the Philippines: a–d, four perspectives of an A. hians shell from the Philippines (79.6 mm shell length [P], BMNH unreg., "Cuming, i.") displaying a clear shift from Type 1 shell formation (T1) to Type 2 shell formation (T2) indicated by a reduction in the size and spacing of the keel tubercles, a reduction in the ratio of ribs to keel tubercles (from approximately 1.5:1 to 1:1) and subsumed ears; a, right lateral view; b, anterior aperture view; c, posterior keel view; d, ventro-posterior keel view. Scale bar = 1 cm.
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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.