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Fig. 1 in Phylogenetic analysis and systematics of the Acrapex unicolora Hampson species complex (Lepidoptera, Noctuidae, Noctuinae, Apameini), with the description of Fve new species from the Afrotropics
Fig. 1. Adults of species of Acrapex. – A–F. A. cuprescens (Hampson, 1910). A. ♂, upper side. B. ♂, under side. C. ♂, original labels from BMNH. D. ♀, original labels from BMNH. E. Upper side. F. Under side. – G–J. A. kafula le Ru sp. nov. G. ♂, upper side. H. ♂, under side. I. ♀, upper side. J. ♀, under side. Scale bars = 3 mm.
Fig. 2 in Phylogenetic analysis and systematics of the Acrapex unicolora Hampson species complex (Lepidoptera, Noctuidae, Noctuinae, Apameini), with the description of Fve new species from the Afrotropics
Fig. 2. Male genitalia of species of Acrapex. – A, I. A. cuprescens (Hampson, 1910). – B, J. A. kafula le Ru sp. nov. – C, K. A. kavumba le Ru sp. nov. – D, L. A. kiakouama le Ru sp. nov. – E, M. A. malagasy Viette, 1967. – F, N. A. mediopuncta (Bowden, 1956). – G, O. A. parvaclara Berio, 1973. – H, P. A. unicolora (Hampson, 1910). Scale bars = 0.5 mm.
Fig. 1 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 1. Oxidus gracilis (C.L. Koch, 1847) from Okinawa Island, Japan. A. Entire body, length ca 23 mm. B–C. Segments 8–9–10. B. ♂. C. ♀. Scale bars = 1 mm. (photos by Z. Korsós)
Fig. 2 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 2. Left gonopod of Oxidus gracilis (C.L. Koch, 1847), sample IEBR-USA. A. Lateral view. B. Mesal view. Scale bars = 100 µm.
Fig. 6 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 6. Left gonopod of Oxidus riukiaria (Verhoeff, 1940). A. Lateral view. B. Postfemoral region, lateral view. Redrawn from Verhoeff 1940. No scale bars.
Fig. 4 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 4. Right gonopod of Oxidus gigas (Attems, 1953), from sample IEBR-Myr 113. A. Lateral view. B. Ventral view. C. Mesal view. The picture has been Fipped horizontally. Scale bars = 1 um.
Fig. 5 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 5. Oxidus riukiaria (Verhoeff, 1940) from Okinawa, Japan. A. Entire body, length ca 20 mm. B–C. Segments 8–9–10. B. ♂. C. ♀. Scale bars = 1 mm. (photos by Z. Korsós)
Fig. 8. A in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 8. A. Left gonopod of Oxidus avia (Verhoeff, 1937), lateral view. B. Right gonopod of Oxidus obtusus (Takakuwa, 1942), mesal view. Redrawn from Verhoeff 1937 and Takakuwa 1942a, respectively. No scale bars.
Fig. 3 in A phylogenetic analysis of the heterostracan jawless vertebrate family Cyathaspididae
Fig. 3. Phylogeny of the Cyathaspididae as a strict consensus tree from two most parsimonious trees (Length 142, Consistency Index 0.4366, Retention Index 0.6244) using unordered and unweighted characters (35) and 29 cyathaspid taxa with one outgroup (Athenaegis chattertoni). Subline numbers represent bootstrap support values as further described in the text.
Fig. 1 in A phylogenetic analysis of the heterostracan jawless vertebrate family Cyathaspididae
Fig. 1. Terminology for features of the cephalothorax in the Cyathaspididae. A–C. Terminology for the main plates and sensory canal system of the cephalothorax based on Poraspis, in dorsal (A), ventral (B), and lateral (C) views; after Denison (1964). D, E. Sensory canal systems in the dorsal plates of Tolypelepis (D) and Dikenaspis (E); after Denison (1964). F. Illustration of the position of the lateral brim and lateral lamina. G. Position of the epitega, postrostral field, and pineal macula in Vernonaspis bryanti; after Denison (1964).
Fig. 2. Consensus trees for the Cyathaspididae. A in A phylogenetic analysis of the heterostracan jawless vertebrate family Cyathaspididae
Fig. 2. Consensus trees for the Cyathaspididae. A, after Lundgren and Blom (2013); B, after Randle and Sansom (2017); C, after Denison (1964). Taxa not used in the analysis in this paper are denoted by an asterisk (*).
Fig. 7 in Ultrastructure and 28S rDNA Phylogeny of Two Gregarines: Cephaloidophora cf. communis and Heliospora cf. longissima with Remarks on Gregarine Morphology and Phylogenetic Analysis
Fig. 7. Relative rates of molecular evolution in long-branch apicomplexans: SSU rDNA (white columns) and LSU rDNA (black columns), calculated as ratio of the length of the current branch to average branch length of the non-long-branch apicomplexans (see the text for more explanations). Relative rates of LSU rDNA evolution are lower than those of SSU rDNA, especially in gregarines.
Fig. 2 in Ultrastructure and 28S rDNA Phylogeny of Two Gregarines: Cephaloidophora cf. communis and Heliospora cf. longissima with Remarks on Gregarine Morphology and Phylogenetic Analysis
Fig. 2. Light microscopy of the gregarine studied: free individuals (gamonts) of Cephaloidophora cf. communis (A, common light microsopy; B, DIC microscopy); a free gamont (C) and a syzygy (D) of Heliospora cf. longissima. Epimerite (ep), promerite (pr), deutomerite (de), septum between poto- and deutomerite (s1), and septum between proto- and epimerite (s2) are visible.
Fig. 1 in Ultrastructure and 28S rDNA Phylogeny of Two Gregarines: Cephaloidophora cf. communis and Heliospora cf. longissima with Remarks on Gregarine Morphology and Phylogenetic Analysis
Fig. 1. Layout of ribosomal operon fragment amplifications. Up- per part, schematic ribosomal operon with approximate positions of the direct and reverse primers used. Lower part, the amplified fragments of ribosomal DNA aligned with the ribosomal operon (above). Numbers indicate the length of the overlapping regions. Roman numerals denote the fragments discussed in this paper. SSU rDNA fragments analyzed previously by Rueckert et al. (2011b) have no numerical designations.
Fig. 3. Agarose gel image Fig. 4 in Optimization Of Dna Extraction Protocol For Dna Isolation From Air-Dried Collection Material For Further Phylogenetic Analysis (Coleoptera: Carabidae)
Fig. 3. Agarose gel image Fig. 4. Agarose gel image (successful PCR amplification) (failed PCR amplification) M: marker (bp) M: marker (bp) A1: Agonum fuliginosum Panzer, 1809 A: Agonum fuliginosum Panzer, 1809 A2: Agonum thoreyi Dejean, 1828 O: Omophron aequale aequale Morawitz, 1863 O: Omophron aequale aequale Morawitz, 1863 N: Notiophilus semistriatus Say, 1823 N: Notiophilus semistriatus Say, 1823 Nk: negative control. Nk: negative control.
Fig. 1 in Optimization Of Dna Extraction Protocol For Dna Isolation From Air-Dried Collection Material For Further Phylogenetic Analysis (Coleoptera: Carabidae)
Fig. 1. Photo of Omophron aequale jacobsoni Fig. 2. Photo of Omophron aequale jacobsoni Semenov, 1922 before incubation. Semenov, 1922 after 16 h (56°C) incubation time in tissue lysis buffer with proteinase K.
FIGURE 32 in Phylogenetic analysis and taxonomic revision of Physodactylinae (Coleoptera, Elateridae)
FIGURE 32: Teslasena femoralis. A, maxilla; B, detail of maxillar base; C, labium; D, pronotum (laterodorsal); E, pronotal punctation; F, elytral striae; G, elytron (dorsolateral); H, I, J, pro-, meso and metathoracic legs; K, protarsus; L, claw.
FIGURE 24 in Phylogenetic analysis and taxonomic revision of Physodactylinae (Coleoptera, Elateridae)
FIGURE 24: Physodactylus henningi. A, tergite VIII; B, sternite VIII; C, ovipositor (ventral); D, ovipositor and reproductive tract (dorsal).
FIGURE 23 in Phylogenetic analysis and taxonomic revision of Physodactylinae (Coleoptera, Elateridae)
FIGURE 23: Physodactylus henningi. A, sternite VIII; B, tergite VIII; C, sternite IX; D, tergites IX and X; E, F, aedeagus (ventral, dorsal).
FIGURE 35 in Phylogenetic analysis and taxonomic revision of Physodactylinae (Coleoptera, Elateridae)
FIGURE 35: Habitus. A, Physodactylus brasiliensis (12.8 mm); B, P. brunneus sp. nov. (9.0 mm); C, P. chassaini sp. nov. (11.5 mm); D, P. costae (12.0 mm); E, P. fischeri (17.0 mm); F, P. flavifrons sp. nov. (10.0 mm); G, P. fleutiauxi (15.0 mm); H, P. foveatostriatus (12.0 mm); I, P. girardi sp. nov. (9.0 mm); J, P. gounellei sp. nov. (10.5 mm); K, P. henningi (15.0 mm); L, P. latithorax sp. nov. (18.0 mm); M, P. niger (11.0 mm); N, P. oberthuri (12.5 mm); O, P. patens sp. nov. (17.0 mm); P,P. pujoli (12.0 mm); Q, P. sulcatus (9.0 mm); R, P. tuberculatus sp. nov. (12.0 mm). A-D, F-J, L-R = holotypes.
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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.