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FIGURE 2 in The identities of three species of Parahelice Sakai, Türkay & Yang, 2006 (Crustacea: Brachyura: Varunidae) from the western Pacific, based on morphological and molecular evidence
FIGURE 2. Parahelice daviei Sakai, Türkay & Yang, 2006. A–C, E–H, ♂ (12.0 × 9.7 mm, NCHUZOOL 15670); D, I, ♀ (13.2 × 10.6 mm, NMMBCD 4049). A, carapace; B, outer view of male right cheliped; C, left male infraorbital ridge; D, left female infraorbital ridge; E, F, dorsal view of right G1; G, H, ventral view of right G1; I, right vulva. Scale bars: A–D, 1.0 mm; E–I, 0.5 mm.
FIGURE 4 in The identities of three species of Parahelice Sakai, Türkay & Yang, 2006 (Crustacea: Brachyura: Varunidae) from the western Pacific, based on morphological and molecular evidence
FIGURE 4. Parahelice pilimana (A. Milne-Edwards, 1873). A–C, E–H, ♂ (10.4 × 8.6 mm, NCHUZOOL 15666); D, I, ♀ (10.7 × 8.9 mm, NCHUZOOL 15668). A, carapace; B, outer view of male left cheliped; C, male left infraorbital ridge; D, female left infraorbital ridge; E, F, dorsal view of right G1; G, H, ventral view of right G1; I, right vulva. Scale bars: A–D, 1.0 mm; E–I, 0.5 mm.
FIGURE 3 in The identities of three species of Parahelice Sakai, Türkay & Yang, 2006 (Crustacea: Brachyura: Varunidae) from the western Pacific, based on morphological and molecular evidence
FIGURE 3. Parahelice pilimana (A. Milne-Edwards, 1873). A, dorsal view of male; B, ventral view of male; C, chela of male; D, chela of female. A–C, ♂ (CW 10.4 mm), D, ♀ (CW 10.7 mm) (NCHUZOOL 15666; Baoli R. estuary, Pingtung, Taiwan). Scale bars: 2.0 mm.
FIGURE 2. Maximum Likelihood tree with branch lengths, inferred from a 3,649 in Tachiramantis lassoalcalai (Barrio-Amorós, Rojas-Runjaic & Barros, 2010) (Anura, Craugastoridae): a new combination revealed by molecular evidence, with a description of its advertisement call
FIGURE 2. Maximum Likelihood tree with branch lengths, inferred from a 3,649 bp fragment of the mitochondrial genes 12S rRNA, 16S rRNA, and the nuclear RAG1 and Tyr, depicting phylogenetic relationships of Tachiramantis lassoalcalai comb. nov. with Tachiramantis and some selected species of other 17 Terrarana genera. Bootstrap support values higher than 50 % are presented for each node. Values of 100 % are represented by an asterisk.
FIGURE 17 in Molecular and morphological evidence reveals three species within the California sister butterfly, Adelpha bredowii (Lepidoptera: Nymphalidae: Limenitidinae)
FIGURE 17. One of 397 most parsimonious trees obtained through parsimony analysis, based on 658 bp of COII and 325 bp of Tpi combined into a single matrix (L = 180 steps, CI = 0.87). Allele numbers (COII, Tpi) correspond to those listed in Tables 1 and 2, respectively. All samples included sequence data from COII, but not all included Tpi. Those without Tpi are listed as 0. Parsimony bootstrap/Bayesian posterior probabilities above 80/0.80 are indicated above or adjacent to branches. Trees rooted with Adelpha lycorias, A. mesentina, and A. phylaca.
FIGURE 2 in Molecular evidence of the taxonomic status of western Mexican populations of Phaethornis longirostris (Aves: Trochilidae)
FIGURE 2. Haplotype and allele networks for each mtDNA and nDNA marker of the Mexican samples. The map depicts in gray the range of P. longirostris 'sensu lato' in Mexico; highlands are depicted in yellow. Color points indicate the sample localities and correspond to the colors in the networks. The square indicates samples obtained from the GenBank.
FIGURE 3 in Morphological, biogeographical and molecular evidence of Carpocoris mediterraneus as a valid species (Hemiptera: Pentatomidae)
FIGURE 3. Antero-dorsal views of A) C. fuscispinus. B) C. mediterraneus atlanticus. Red arrows indicates a more pronounced concavity of the anterolateral margin of the pronotum in C. mediterraneus atlanticus. The posterolateral margin is more convex in C. fuscispinus. Hence, the convexity (shown by green lines) further exceeds in C. fuscispinus the red line drawn between the humeral angle of the pronotum and the humeral angle of the scutellum. The distance between the anterior margin of the pronotum and the dotted red line, drawn between the humeral angles, is shorter in C. fuscispinus (usually less than a third of the length of pronotum).
FIGURE 1 in Morphological, biogeographical and molecular evidence of Carpocoris mediterraneus as a valid species (Hemiptera: Pentatomidae)
FIGURE 1. European distribution of Carpocoris fuscispinus (Boheman, 1851) according to Tamanini (1959). The shaded part represents the area where the species was found. Question marks from Tamanini where the distribution was questionable.
Figure 90 in Phylogeny of the spider genus Ixchela Huber, 2000 (Araneae: Pholcidae) based on morphological and molecular evidence (CO1 and 16S), with a hypothesized diversification in the Pleistocene
Figure 90. Known records of Ixchela azteca sp. nov., Ixchela jalisco sp. nov., Ixchela mendozai sp. nov., Ixchela purepecha sp. nov. and Ixchela tlayuda sp. nov.
Figures 1–9 in Phylogeny of the spider genus Ixchela Huber, 2000 (Araneae: Pholcidae) based on morphological and molecular evidence (CO1 and 16S), with a hypothesized diversification in the Pleistocene
Figures 1–9. Ixchela azteca sp. nov. (1–6) and Ixchela mendozai sp. nov. (7–9). 1, Left palp showing bulb, PAB and embolus, prolateral view. 2, 3, Embolus, prolateral–dorsal view (arrow indicates the spine on sperm duct). 4, 6, Embolus, prolateral and retrolateral views, respectively (arrow indicates the spine-shaped projections). 5, 7, Details of the spineshaped projections on embolus. 8, Embolus, distal view (arrow indicates the spine-shaped projections). 9, Embolus, retrolateral view (arrow indicates the sub-distal, sclerotized spine). Scale bars: 30 μm (Fig. 7), 50 μm (Fig. 5), 100 μm (Figs 3, 8, 9), 200 μm (Figs 2, 4, 6), 500 μm (Fig. 1).
Figures 18–25 in Phylogeny of the spider genus Ixchela Huber, 2000 (Araneae: Pholcidae) based on morphological and molecular evidence (CO1 and 16S), with a hypothesized diversification in the Pleistocene
Figures 18–25. Ixchela azteca sp. nov. Male. 18, Left patella IV, ventral view (arrow indicates the lyriform organs). 19, Left patella IV, detail of the lyriform organs. 20, Left tibia IV, basal part, ventral view. 21, Tibia IV, detail of the setae. 22, Left tarsus IV, retrolateral view (arrows indicate the comb-hairs). 23, Left tarsus IV, detail of the median claw and comb-hairs. 24, Left tarsus IV, detail of the pseudosegments (arrow indicates the tarsal organ). 25, Left tarsus IV, detail of the tarsal organ and setae socket. Scale bars: 30 μm (Figs 23, 25), 50 μm (Figs 19, 22), 100 μm (Fig. 24), 300 μm (Fig. 21), 400 μm (Fig. 18), 500 μm (Fig. 20).
Figures 10–17 in Phylogeny of the spider genus Ixchela Huber, 2000 (Araneae: Pholcidae) based on morphological and molecular evidence (CO1 and 16S), with a hypothesized diversification in the Pleistocene
Figures 10–17. Ixchela jalisco sp. nov. (10–14, 17) and Ixchela mendozai sp. nov. (15, 16). 10, Trichobothria of the tibia, male palp. 11, Trichobothria socket, detail. 12, Female left palp, showing trichobothria on tibia. 13, Female left palp (arrow indicates the setae on tarsus). 14, Male palp, detail of basal setae on dorsal area of procursus. 15, Setae on ventrobasal protuberance of procursus. 16, Procursus basal part (arrow indicates the exposed tarsal organ). 17, Female left palp (arrow indicates the tarsal organ). Scale bars: 50 μm (Fig. 11), 100 μm (Figs 15, 17), 200 μm (Figs 10, 14), 300 μm (Figs 13, 16), 500 μm (Fig. 12).
FIGURE 5 in A new species of Brassica (Brassicaceae) from Bolkar Mountains (Türkiye) with morphological and molecular evidence
FIGURE 5. Leaf and hair types of Brassica huseyin-duralii, B. elongata, B. repanda and its subspecies, A-B) Brassica huseyin-duralii, C) B. elongata, D) B. repanda (E-00053767), E) subsp. africana (Gómez-Campo 1993), F) subsp. almeriensis (Gómez-Campo 1993), G) subsp. baldensis (Gómez-Campo 1993), H) subsp. blancoana (Gómez-Campo 1993), I) subsp. cadavelli (type, BC-3841), J) subsp. cantabrica (Gómez-Campo 1993), K) subsp. confusa (Gómez-Campo 1993), L) subsp. dertosensis (isotype, BCN-119617), M) subsp. galissieri (P-04657619), N) subsp. glabrescens (GJO-0070104), O) subsp. gypsicola (Gómez-Campo 1993), P) subsp. latisiliqua (GómezCampo 1993), R) subsp. maritima (BM-000792723), S) subsp. saxatilis (P-05331698), T) subsp. silenifolia (type, RAB-017939), U) subsp. turbonis (type, BC-633799).
Figure 21 in Systematics and phylogeny of the hoplonemertean genus Diplomma (Nemertea) based on molecular and morphological evidence
Figure 21. Diplomma serpentina (Stimpson, 1855). A, transverse section through foregut region, showing dorsoventral muscles (indicated by arrowheads); B, transverse section through intestinal region, showing dorsoventral muscles running outside lateral nerve cord (indicated by black arrowhead) and inside ovary (indicated by white arrowheads); C, transverse section through pyloric region – dorsoventral muscles were not evident in this individual; D, transverse section through foregut region, showing dorsoventral muscles (indicated by arrowheads) running outside lateral nerve cord and lateral blood vessel; E, transverse section through foregut region, showing dorsoventral muscles (indicated by arrowhead) running outside excretory tubule. A, B, paraneotype (ZIHU-3166); C, paraneotype (ZIHU-1356); D, E, paraneotype (UPLB- NHM 0488). Abbreviations: DE, dermis; EX, excretory collecting tubule; IC, intestinal caecum; LN, lateral nerve cord; LV, lateral blood vessel; OV, ovum; PA, parenchyma; PY, pylorus; RC, rhynchocoel; ST, stomach. Scale bars: A, B = 50 Mm; C, E = 30 Mm; D = 100 Mm.
Figure 11 in Systematics and phylogeny of the hoplonemertean genus Diplomma (Nemertea) based on molecular and morphological evidence
Figure 11. Diplomma bothwellae comb. nov. (formerly Poseidonemertes bothwellae Gibson, 1982). Holotype (AM W.5890). Magnification of Figure 10 to show the dorsoventral muscle fibres (arrowed). Abbreviations: EP, epithelium; LN, lateral nerve cord; LV, lateral blood vessel; RC, rhynchocoel. Scale bar = 20 Mm.
Figure 17 in Systematics and phylogeny of the hoplonemertean genus Diplomma (Nemertea) based on molecular and morphological evidence
Figure 17. Diplomma serpentina (Stimpson, 1855). A, drawing based on neotype, showing general appearance of body in life; B, C, D, enlargements of cephalic region in dorsal (B), ventral (C), and lateral (D) aspects. Scale bar [refers to (A) only] = 3 mm.
Figure 9 in Systematics and phylogeny of the hoplonemertean genus Diplomma (Nemertea) based on molecular and morphological evidence
Figure 9. Diplomma bothwellae comb. nov. (formerly Poseidonemertes bothwellae Gibson, 1982). Holotype (AM W.5890). Transverse section through the anterior proboscis; arrows indicate the proboscis nerves. Scale bar = 20 Mm.
Figure 16 in Systematics and phylogeny of the hoplonemertean genus Diplomma (Nemertea) based on molecular and morphological evidence
Figure 16. Diplomma serpentina (Stimpson, 1855). A, photograph of narcotized specimen taken in life; B, photograph of the same specimen as (A) before anaesthetization, showing natural shape of head; C, horizontal section through head, showing arrangement of outer portion of body-wall longitudinal musculature and its derivatives; D, horizontal section through head, showing arrangement of inner portion of body-wall longitudinal musculature contributing to proboscis insertion; E, sagittal section through head, showing cephalic retractor muscle fibre derived from inner portion of divided body-wall longitudinal muscle layer. A, B, E, UPLB-NHM 0489; C, D, ZIHU-1354. Abbreviations: AG, acidophilic cephalic gland; BG, basophilic cephalic gland; BR, brain; CO, cerebral organ; CR, cephalic retractor muscle; IL, inner portion of body-wall longitudinal musculature; OL, outer portion of body-wall longitudinal musculature; PI, proboscis insertion; PR, proboscis. Scale bars: A = 3 mm; C, D = 100 Mm; E = 50 Mm.
Figure 1 in Systematics and phylogeny of the hoplonemertean genus Diplomma (Nemertea) based on molecular and morphological evidence
Figure 1. Collecting sites of Diplomma serpentina (Stimpson, 1855) in the present study. 1: Shimoda, where Yamaoka (2005) reported Paranemertes sp. that we regard as synonymous with D. serpentina. 2: Kushimoto, the type locality of Amphiporus insolitus Iwata, 1954a, a species that may be synonymous with D. serpentina.
Figure 25 in Systematics and phylogeny of the hoplonemertean genus Diplomma (Nemertea) based on molecular and morphological evidence
Figure 25. Diplomma serpentina (Stimpson, 1855). A, B, transverse section through stomach, showing seemingly appendage-like appearance of the stomach (indicated by asterisk). A, B, neotype (ZIHU-1352). Abbreviations: LN, lateral nerve cord; PR, proboscis; RC, rhynchocoel; ST, stomach. Scale bars: A, B = 100 Mm.
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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.