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FIGURE 4 in First record of the genus Haritalodes Warren, 1890 and H. derogata (Fabricius, 1775) (Lepidoptera: Crambidae: Spilomelinae) from Türkiye and its morphological and molecular identification
FIGURE 4. The worldwide distribution map of Haritalodes derogata (Fabricius, 1775). The present distribution of H. derogata is shaded in gray; the region colored in green shows the presence of the genus in Micronesia and the region colored in red shows the presence of the species in Türkiye.
FIGURE 3 in First record of the genus Haritalodes Warren, 1890 and H. derogata (Fabricius, 1775) (Lepidoptera: Crambidae: Spilomelinae) from Türkiye and its morphological and molecular identification
FIGURE 3. Haritalodes derogata (Fabricius, 1775) female genitalia; (A) female genitalia general view, (B) close-up of the anterior half of ductus bursae and corpus bursae showing the two semicircular and denticulate signa (scale bar: 1 mm). The single arrow indicates ornamented with wrinkles on the anterior half of ductus bursae, and the paired arrows indicate two semicircular and denticulate signa on corpus bursae.
FIGURE 2 in First record of the genus Haritalodes Warren, 1890 and H. derogata (Fabricius, 1775) (Lepidoptera: Crambidae: Spilomelinae) from Türkiye and its morphological and molecular identification
FIGURE 2. Haritalodes derogata (Fabricius, 1775) male genitalia; (A) male genitalia general view, (B) aedeagus (scale bar:1 mm).
FIGURE 1 in A simple molecular method for rapid identification of commercially used Amblyseius and Neoseiulus species (Acari: Phytoseiidae)
FIGURE 1. Products of endonuclease digestion of the PCR products (ITS1/ITS4 primers): 1, AccB1I; 2, AspLEI; 3, SspI.
FIGURE 8 in Morphological and molecular identification of leptocephali of Taiwanese duckbill conger, Gavialiceps taiwanensis (Chen & Weng, 1967) (Family Congridae)
FIGURE 8. Scatter plots of morphometric proportions (in % PAL) versus PAL of leptocephali (triangles), juveniles (diamonds) and adults (squares) of G. taiwanensis showing the growth trend of each proportion.
FIGURE 7 in Morphological and molecular identification of leptocephali of Taiwanese duckbill conger, Gavialiceps taiwanensis (Chen & Weng, 1967) (Family Congridae)
FIGURE 7. Scatter plots of morphometric proportions (in % TL) versus TL of leptocephali (triangles), juveniles (diamonds) and adults (squares) of G. taiwanensis showing the growth trend of each proportion.
FIGURE 6 in Morphological and molecular identification of leptocephali of Taiwanese duckbill conger, Gavialiceps taiwanensis (Chen & Weng, 1967) (Family Congridae)
FIGURE 6. Cladogram showing Neighbor-joining (NJ) tree of relationship of G. taiwanensis and outgroups based on COI sequences.
FIGURE 2 in Morphological and molecular identification of leptocephali of Taiwanese duckbill conger, Gavialiceps taiwanensis (Chen & Weng, 1967) (Family Congridae)
FIGURE 2. General appearance of G. taiwanensis. A. Adult, ASIZP 61770, 161.3 mm PAL. B. Adult, 208.1 mm PAL
FIGURE 4 in Morphological and molecular identification of leptocephali of Taiwanese duckbill conger, Gavialiceps taiwanensis (Chen & Weng, 1967) (Family Congridae)
FIGURE 4. Dorsal view of head showing pigmentation of G. taiwanensis. A. Leptocephalus, NMMB-P27902, 150+ mm TL. B. Juvenile, NMMB-P27893, 103.2 mm PAL. C. Adult, NMMB-P2814, 172 mm PAL.
FIGURE 1 in Morphological and molecular identification of leptocephali of Taiwanese duckbill conger, Gavialiceps taiwanensis (Chen & Weng, 1967) (Family Congridae)
FIGURE 1. General appearance of G. taiwanensis. A, B. Stage 1, NMMB-P27898, 150 mm TL. C. Stage 2, NMMB-P27901, 137+ mm TL. D. Stage 3, NMMB-P27900, 144 mm TL E. Juvenile, NMMB-P27907, 72.4 mm PAL.
FIGURE 9 in Morphological and molecular identification of leptocephali of Taiwanese duckbill conger, Gavialiceps taiwanensis (Chen & Weng, 1967) (Family Congridae)
FIGURE 9. Scatter plots of morphometric proportions (in % HL) versus HL of leptocephali (triangles), juveniles (diamonds) and adults (squares) of G. taiwanensis showing the growth trend of each proportion.
FIGURE 5 in Morphological and molecular identification of leptocephali of Taiwanese duckbill conger, Gavialiceps taiwanensis (Chen & Weng, 1967) (Family Congridae)
FIGURE 5. Close-up view of lateral side of body showing the pigmentation of G. taiwanensis. A. Stage 1, NMMB-P27898, 150 mm TL. B. Stage 2, NMMB-P27901, 137+ mm TL. C. Stage 3, NMMB-P27900, 144 mm TL. D. Juvenile, NMMB- P27893, 95.9 mm PAL. E. Adult, ASIZP 61770, 161.3 mm PAL.
FIGURE 3 in Morphological and molecular identification of leptocephali of Taiwanese duckbill conger, Gavialiceps taiwanensis (Chen & Weng, 1967) (Family Congridae)
FIGURE 3. Lateral view of head showing jaw development of G. taiwanensis. A. Stage 1, NMMB-P27898, 150 mm TL. B. Stage 2, NMMB-P27901, 137+ mm TL. C. Stage 3, NMMB-P27900, 144 mm TL. D. Juvenile, NMMB-P27907, 72.4 mm PAL. E. Adult, ASIZP61770, 161.3 mm PAL.
FIGURE 2 in Morphological and molecular identification of Myxobolus parakoi sp. nov. (Myxozoa: Myxobolidae), from Cyprinus carpio in Chongqing China
FIGURE 2. ML and BI phylogenetic tree based on SSU rDNA sequences of Myxobolus/Henneguya closely related to Myxobolus parakoi sp. nov.. Numbers given at nodes of branches are bootstrap support (BS) and Bayesian posterior probabilities (PP). The new species in the present study is indicated in bold. The arrow points to the shape of the different spores. "//" is shortened to one third of the original length.
FIGURE 1 in Morphological and molecular identification of Myxobolus parakoi sp. nov. (Myxozoa: Myxobolidae), from Cyprinus carpio in Chongqing China
FIGURE 1. Mature spores of Myxobolus parakoi sp. nov.. (A) Single spore. (B) Multiple spores. (C) Schematic illustrations of Myxobolus parakoi sp. nov. in frontal view. Scale bar = 10 μm.
FIGURE S1 in Morphological and molecular identification of Myxobolus parakoi sp. nov. (Myxozoa: Myxobolidae), from Cyprinus carpio in Chongqing China
FIGURE S1. Regions of alignment of SSU rDNA gene sequences of M. koi, M. orissae, M. tanakai and Myxobolus parakoi sp. nov.. Matched sites are represented by dots. Regions are separated by vertical lines.
Fig. 2 Morphological characteristics. a Double broken infraorbital ridge IOR. b in Molecular identification and morphological characteristics of native and invasive Asian brush-clawed crabs (Crustacea: Brachyura) from Japanese and German coasts: Hemigrapsus penicillatus (De Haan, 1835) versus Hemigrapsus takanoi Asakura & Watanabe 2005
Fig. 2 Morphological characteristics. a Double broken infraorbital ridge IOR. b Symmetrically arranged spots on the dorsal face. c Male pleon fold down, first pleopods facing distal/ lateral (setae of the head around a scoop-like nose appears as dark area at the end of the pleopod). d Soft hair near the movable finger of a female chela (HtY2)
Fig. 6 a–g in Polyphyly of the grass tribe Hainardieae (Poaceae: Pooideae): identification of its different lineages based on molecular phylogenetics, including morphological and cytogenetic characteristics
Fig. 6 a–g Mitotic metaphase chromosomes. of a Deschampsia cespitosa (2n = 26). b Festuca gigantea 2n = 42. c Hainardia cylindrica 2n = 26. d Phleum phleoides (2n =14+ 2B). e Vulpia bromoides (2n = 14). f Koeleria cristata (2n = 56). g Colpodium versicolor (2n = 4)
Fig. 4 a–h in Polyphyly of the grass tribe Hainardieae (Poaceae: Pooideae): identification of its different lineages based on molecular phylogenetics, including morphological and cytogenetic characteristics
Fig. 4 a–h Spikelet details. Palea of a Hainardia cylindrica and b Parapholis incurva with glabrous keels (nerves). c, d florets of Narduroides salzmannii with glabrous callus of the lemmas and long rachilla internodes. e, f Agropyropsis lolium with glabrous callus of the lemma (e) and ciliolate keels of the palea (f). g, h Scribneria bolanderi with lemma awned from a sinus of the lemma tip (g) and hairy callus (h). The margin of the lemma is marked at one side in a, b, and f with arrows. Material used: a fruits from Göttingen Botanical Garden in 2006, no. 1850 (HAL); b Röser 2517 (HAL); c Hernández s.n. (C); d Rivas-Martínez s.n. (BASBG); e, f Cosson s.n. (JE); g, h Wilken 16163 and Painter (RSA 695253)
FIGURE 1 in Morphological and molecular identification of a new species of Perenniporia (Polyporales, Basidiomycota) in North America
FIGURE 1. Maximum Parsimony strict consensus tree illustrating the phylogeny of Perenniporia bostonensis and related species based on ITS+nLSU sequences. Branches are labeled with maximum likelihood bootstrap higher than 70%, parsimony bootstrap proportions higher than 50% and Bayesian posterior probabilities more than 0.95 respectively.
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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.