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FIGURE 2 in Ainsliaea polystachya (Asteraceae), a new species from Fujian, China based on morphological and molecular evidence
FIGURE 2. Holotype of Ainsliaea polystachya.
FIGURE 4 in Resurrection of the genus Similisinocarum (Apiaceae) based on evidence from morphology and ITS sequences
FIGURE 4. Types of Similisinocarum normanianum. A. Holotype; B. Isotype.
Figure 15 in Revision of the genus Bosmina Baird, 1845 (Cladocera: Bosminidae), based on evidence from male morphological characters and molecular phylogenies
Figure 15. Bosmina (Lunobosmina) oriens: adult male from a pond on highway 1, Newfoundland, Canada (A, B, D–F, H, I), and from Hell Hollow Pond, Connecticut, USA (C, G, J). A, B, lateral view; C–E, head, lateral view; F, G, head, anterior view; H–J, mucro, inner view. Scale bars: 100 Mm.
Figure 3. A in The taxonomic status of some Atlanto-Mediterranean species in the subgenus Holothuria (Echinodermata: Holothuroidea: Holothuriidae) based on molecular evidence
Figure 3. A, distribution of 49 individuals of the Holothuria subgenus and four of Holothuria sanctori in the space defined by the first two axes of the principal components (PC) analysis on the basis of morphometric variables of the ossicles. The symbols indicate assignment to the three identified clades; labels of the individuals indicate the preliminary species identified (st, Holothuria stellati; m, Holothuria mammata; t, Holothuria tubulosa; d, Holothuria dakarensis; and s, Holothuria sanctori) and the locality according to Figure 1. B, the most important variables are presented. PC1 (+): mTArHdt, mTArHvt, mAdt, mAvt, mTArHvb. PC1 (-): sdXDHdt, sdNDHdt, mESIvb. PC2 (+): mESIdb, nESIdb, mArCvt. PC2 (-): mNHdb, sdPvb, sdXDvb, mPdb (see Table 2 and Appendix S1 for the meaning of the abbreviations of the variables).
Figure 5 in Phylogeny of the genera of the parasitic wasps subfamily Doryctinae (Hymenoptera: Braconidae) based on morphological evidence
Figure 5. External morphological features in the Doryctinae. A–D, Hind coxa; E, hind coxa, trochanter, trochantellus and femur; F, fore femur; G, fore femur, tibia and basitarsus; H, I, J, hind tibia. A, J, Bracodoryctes tergalis Belokobylskij & Quicke; B, I, Sonanus senzuensis Belokobylskij & Konishi; C, Priosphys denticulata Enderlein; D, Liodoryctes australiensis (Szépligeti); E, F, Termitospathius sumatranus Belokobylskij; G, Ceylonspathius nixoni Belokobylskij; Rhoptrocentrus cleopatrae Belokobylskij.
Figure 1 in Phylogeny of the genera of the parasitic wasps subfamily Doryctinae (Hymenoptera: Braconidae) based on morphological evidence
Figure 1. External morphological features in the Doryctinae. A–C, head, dorsal view; D–F, head, frontal view; G–N, basal and apical segments of antenna (dorsal and lateral views). A, Rhoptrocentrus cleopatrae Belokobylskij; B, M, N, Sonanus senzuensis Belokobylskij & Konishi; C, Bracodoryctes tergalis Belokobylskij & Quicke; D, Doryctes germanicus Belokobylskij; E, Stephanospathius ornatipes (Kieffer); F, Schlettereriella rufithorax (Szépligeti); G, Platyspathius hospitus Belokobylskij & Ku; H, J, Synspilus nitidus Belokobylskij & Quicke; I, K, Binarea spinicollis Brullé; L, Ecphylus brevitergum Belokobylskij.
Figure 2 from: Duan L, Han L-N, Sirichamorn Y, Wen J, Compton JA, Deng S-W, Arslan E, Ertuğrul K, Schrire B, Chen H-F (2021) Proposal to recognise the tribes Adinobotryeae and Glycyrrhizeae (Leguminosae subfamily Papilionoideae) based on chloroplast phylogenomic evidence. PhytoKeys 181: 65-77. https://doi.org/10.3897/phytokeys.181.71259
Figure 2 Bayesian maximum clade credibility tree of the GAW clade and related groups based on chloroplast CDSs. Bayesian posterior probabilities are given above branches, Maximum Likelihood bootstrap values below branches. Asterisks indicate PP = 1 and LBS = 100%. W. nieuwenhuisii indicates Whitfordiodendron nieuwenhuisii.
Figure 1 from: Duan L, Han L-N, Sirichamorn Y, Wen J, Compton JA, Deng S-W, Arslan E, Ertuğrul K, Schrire B, Chen H-F (2021) Proposal to recognise the tribes Adinobotryeae and Glycyrrhizeae (Leguminosae subfamily Papilionoideae) based on chloroplast phylogenomic evidence. PhytoKeys 181: 65-77. https://doi.org/10.3897/phytokeys.181.71259
Figure 1 Representative plants of Adinobotryeae and Glycyrrhizeae. Inflorescences (A) and fruits (B) of Adinobotrys atropurpureus; inflorescence (C) and infructescence (D) of Glycyrrhiza pallidiflora; inflorescence (E) and infructescence (F) of Glycyrrhiza uralensis; fruits (G) of Glycyrrhiza inflata; inflorescence (H) and part of dried infructescence [I; photographed on herbarium specimen: A. Eustace 31 (E!)] of Glycyrrhizopsis flavescens.
Figure 7 from: von Konrat M, de Lange P, Greif M, Strozier L, Hentschel J, Heinrichs J (2012) Frullania knightbridgei, a new liverwort (Frullaniaceae, Marchantiophyta) species from the deep south of Aotearoa-New Zealand based on an integrated evidence-based approach. PhytoKeys 8: 13-36. https://doi.org/10.3897/phytokeys.8.2496
Figure 7 - Frullania knightbridgei A, B Main stem, ventral view. A Main stem and lateral branches, lobules subparallel in relation to the stem and occupying ca. 25% of the exposed surface of the dorsal lobe B iIllustrating terminal position of the gynoecium with 2 subfloral branches immediately below C Bicoloured leaf-lobules D Initial branching appendages E Median cells of the leaf-lobe with subequally thickened cell walls F Basal cells of the leaf-lobe. Scale bars A = 200 µm; B = 500 µm; C,D = 50 µm; E, F = 10 µm.
Figure 5 from: von Konrat M, de Lange P, Greif M, Strozier L, Hentschel J, Heinrichs J (2012) Frullania knightbridgei, a new liverwort (Frullaniaceae, Marchantiophyta) species from the deep south of Aotearoa-New Zealand based on an integrated evidence-based approach. PhytoKeys 8: 13-36. https://doi.org/10.3897/phytokeys.8.2496
Figure 5 - Epidermal layer of the capsule wall and spore surface ultrastructure. A Epidermal layer of Frullania knightbridgeiB Epidermal layer of Frullania rostrataC, E Spore surface of Frullania knightbridgeiD, F Spore surface of Frullania rostrata.Scale bars A, B = 10 µm; C = 2 µm; D = 5 µm; E,F = 1 µm.
Figure 4 from: von Konrat M, de Lange P, Greif M, Strozier L, Hentschel J, Heinrichs J (2012) Frullania knightbridgei, a new liverwort (Frullaniaceae, Marchantiophyta) species from the deep south of Aotearoa-New Zealand based on an integrated evidence-based approach. PhytoKeys 8: 13-36. https://doi.org/10.3897/phytokeys.8.2496
Figure 4 - Lobule position and styli. A Frullania rostrata B Frullania truncatistyla C Frullania magellanica D Frullania knightbridgeiScale barsA, D = 50 µm; B = 20 µm; C = 100 µm.
Figure 3 from: von Konrat M, de Lange P, Greif M, Strozier L, Hentschel J, Heinrichs J (2012) Frullania knightbridgei, a new liverwort (Frullaniaceae, Marchantiophyta) species from the deep south of Aotearoa-New Zealand based on an integrated evidence-based approach. PhytoKeys 8: 13-36. https://doi.org/10.3897/phytokeys.8.2496
Figure 3 - Oil bodies in a leaf shoot of Frullania knightbridgei illustrating, in region of arrow, the 1–2 large oil bodies per cell. Scale bar = 20 µm.
Figure 2 from: von Konrat M, de Lange P, Greif M, Strozier L, Hentschel J, Heinrichs J (2012) Frullania knightbridgei, a new liverwort (Frullaniaceae, Marchantiophyta) species from the deep south of Aotearoa-New Zealand based on an integrated evidence-based approach. PhytoKeys 8: 13-36. https://doi.org/10.3897/phytokeys.8.2496
Figure 2 - Variation in characters associated with the leaf-lobe oil bodies and leaf-lobule anatomy (A, B, E Frullania knightbridgei; C, D, F Frullania rostrata) A Oil bodies of the median region of the leaf-lobe, very large, (1)2–(3) per cell, collectively occupying over 75% of the cell lumen B Oil bodies of basal cells, a characteristic group of basal ocelli, each ocellus almost occupying the entire cell lumen C Oil bodies of median cells, 2–3 per cell, collectively occupying very small area of cell lumen, lacking any significant ornamentation and appearing as almost homogeneous oil droplets D Oil bodies of basal cells, 3–5 per cell E Semi straight cell walls toward apex leaf-lobule F Flexuose cell walls towards apex of leaf lobule. Scale bars A, B = 15 µm; C–F = 10 µm.
Figure 1 from: von Konrat M, de Lange P, Greif M, Strozier L, Hentschel J, Heinrichs J (2012) Frullania knightbridgei, a new liverwort (Frullaniaceae, Marchantiophyta) species from the deep south of Aotearoa-New Zealand based on an integrated evidence-based approach. PhytoKeys 8: 13-36. https://doi.org/10.3897/phytokeys.8.2496
Figure 1 - Maximum likelihood phylogeny (ln = -2984.6458) derived from an nrITS2 – trnL-F sequence alignment including 14 new sequences and 18 sequences from Hentschel et al. (2009). ML bootstrap percentage values (> 50) in bold face, MP bootstrap percentage values (>50) not bold.
Figure 7 from: Alwan NH, Zareian H, Esmaeili HR (2016) Capoeta coadi, a new species of cyprinid fish from the Karun River drainage, Iran based on morphological and molecular evidences (Teleostei, Cyprinidae). ZooKeys 572: 155-180. https://doi.org/10.3897/zookeys.572.7377
Figure 7 - Bayesian tree inferred from COI. Numbers left of the slash, indicate the posterior probabilities of the Bayesian analysis, using MrBayes, while numbers right of the slash are the bootstrap support for 10,000 replicates in the Maximum Likelihood tree, using RaxML. Asterisks (*) indicate less than 50% Maximum Likelihood support and (-) indicates less than 0.50 Bayesian posterior probabilities for the node.
Figure 4 from: Alwan NH, Zareian H, Esmaeili HR (2016) Capoeta coadi, a new species of cyprinid fish from the Karun River drainage, Iran based on morphological and molecular evidences (Teleostei, Cyprinidae). ZooKeys 572: 155-180. https://doi.org/10.3897/zookeys.572.7377
Figure 4 - Dorsal fins of Capoeta coadi sp. n. a ZM-CBSU J 444; 73 mm SL b ZM-CBSU Z195; 104 mm SL c ZM-CBSU Z192; 148 mm SL; Iran: Kohgiluyeh and Boyer Ahmad, Beshar River, Karun River drainage, to show size-dependent variability of the last simple dorsal-fin ray serration.
Figure 3 from: Alwan NH, Zareian H, Esmaeili HR (2016) Capoeta coadi, a new species of cyprinid fish from the Karun River drainage, Iran based on morphological and molecular evidences (Teleostei, Cyprinidae). ZooKeys 572: 155-180. https://doi.org/10.3897/zookeys.572.7377
Figure 3 - Live specimen of Capoeta coadi sp. n, Iran: Kohgiluyeh and Boyer Ahmad, Beshar River, Karun River drainage.
Figure 2 from: Alwan NH, Zareian H, Esmaeili HR (2016) Capoeta coadi, a new species of cyprinid fish from the Karun River drainage, Iran based on morphological and molecular evidences (Teleostei, Cyprinidae). ZooKeys 572: 155-180. https://doi.org/10.3897/zookeys.572.7377
Figure 2 - Capoeta coadi sp. n., paratypes: a ZM-CBSU Z191; 157 mm SL b ZM-CBSU Z192, 148 mm SL; Iran: Kohgiluyeh and Boyer Ahmad, Beshar River, Karun River drainage.
Figure 1 from: Alwan NH, Zareian H, Esmaeili HR (2016) Capoeta coadi, a new species of cyprinid fish from the Karun River drainage, Iran based on morphological and molecular evidences (Teleostei, Cyprinidae). ZooKeys 572: 155-180. https://doi.org/10.3897/zookeys.572.7377
Figure 1 - Capoeta coadi sp. n., ZM-CBSU Z190, holotype, 157 mm SL; Iran: Kohgiluyeh and Boyer Ahmad, Beshar River, Karun River drainage.
Figure 6 from: Alwan NH, Zareian H, Esmaeili HR (2016) Capoeta coadi, a new species of cyprinid fish from the Karun River drainage, Iran based on morphological and molecular evidences (Teleostei, Cyprinidae). ZooKeys 572: 155-180. https://doi.org/10.3897/zookeys.572.7377
Figure 6 - Bayesian tree inferred from cyt b. Numbers left of the slash, indicate the posterior probabilities of the Bayesian analysis, using MrBayes, while numbers right of the slash are the bootstrap support for 10,000 replicates in the Maximum Likelihood tree, using RaxML. Asterisks (*) indicate less than 50% Maximum Likelihood support for the node.
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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.