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Fig. 3 in Systematics, Morphology and Biogeography Phylogeny of the Augochlora clade with the description of four new species (Hymenoptera, Apoidea)
Fig. 3. Paratypemaleof Augochlorellakelliae sp. nov.(A) Dorsalview; (B) frontalview of head; (C) ventral view of genitalia. Scale bar: Aand Bat 0.5 mm, Cat 0.25 mm.
FIG. 1 in Beyond shells: first detailed morphological description of the mangrove-associated gastropod Haminoea cf. fusca (A. Adams, 1850) (Cephalaspidea, Haminoeidae), with a COI phylogenetic analysis
FIG. 1. — Bayesian phylogenetic tree based on partial sequences of the COI gene. Figures on nodes are posterior probabilities, scale bar refer to branch lengths. Coloured squares refer to species that are Indo West Pacific in origin, whereas grey squares to Atlantic and eastern Pacific species. PP, 1. The specimen here used from the Philippines is depicted in Gosliner et al. 2015: 30, lower right.
Fig. 10. Dendrobium letocartiorum Munzinger & M in Morphological and anatomical investigation of New Caledonian graminoid Dendrobium (Orchidaceae) with the description of two new species
Fig. 10. Dendrobium letocartiorum Munzinger & M.Pignal sp. nov. A. Habit. B. Flower, profile. C. Flower, lateral sepal removed. D. Lateral sepal. E. Dorsal sepal. F. Petal. G. Lip. H. Column. I. Fruit. J. Seed. Scale bar: A = 2 cm, B, I = 1 cm, C–H = 5 mm, J = 40 μm (A. Mouly 99, holotype [P00777176]). Drawing by Dominique Storez.
Fig. 9 in Morphological and anatomical investigation of New Caledonian graminoid Dendrobium (Orchidaceae) with the description of two new species
Fig. 9. Distribution of D. butinii M.Pignal & Munzinger, sp. nov., based on herbarium specimens (●) and field observations (), 'T' indicates the type collection.
Fig. 5 in Morphological and anatomical investigation of New Caledonian graminoid Dendrobium (Orchidaceae) with the description of two new species
Fig. 5. Stomata (SEM). A–B. Type I: D. camaridiorum Rchb.f. (H.S. MacKee 14228). C. Type I: D. butinii M.Pignal & Munzinger sp. nov. (M. Pignal 2384). D. Type II: D. butinii M.Pignal & Munzinger sp. nov. (M. Pignal 2384). E. Type I: D. crassifolium Schltr. (H.S. MacKee 43781). F. Type II: D. crassifolium Schltr. (H.S. MacKee 43781). G. Type II: D. letocartiorum Munzinger & M.Pignal sp. nov. (H.S. MacKee 37760). H. Type II: D. unicarinatum Kores (H.S. MacKee 36986). Scale bars = 10 μm.
Fig. 3 in Morphological and anatomical investigation of New Caledonian graminoid Dendrobium (Orchidaceae) with the description of two new species
Fig. 3. Seeds, opening on the right. A–B. D. camaridiorum Rchb.f. A. LM. B. SEM (H.S. MacKee 14228). C–D. D. butinii M.Pignal & Munzinger sp. nov. C. LM. D. SEM (M. Pignal 2384). E–G. D. letocartiorum Munzinger & M.Pignal sp. nov. E. SEM. F. LM. G. SEM (H.S. MacKee 37760). H–I. D. unicarinatum Kores. H. SEM (H.S. MacKee 36986). I. LM (H.S. MacKee 44925). Scale bars: A–F, H–I = 10 μm; G = 30 μm.
Fig. 1. Morphological characters used for the phylogenetic analysis and key. A–C. Terminal maxillary palpomere. D–E. Eyes. F–H. Pronotum. I–J. Leg. K–L in Taxonomic revision of the Lycocerus hanatanii species group (Coleoptera, Cantharidae), with the description of new species from Taiwan
Fig. 1. Morphological characters used for the phylogenetic analysis and key. A–C. Terminal maxillary palpomere. D–E. Eyes. F–H. Pronotum. I–J. Leg. K–L. Inner margin of dorsal plate of aedeagus.
Fig. 13 in Comparative morphology of the endophallic structures of the genus Laius (Coleoptera, Melyridae), with the descriptions of three new species
Fig. 13. Habitat and habits of Laius spp. A. Type locality (Nusa Dua, Bali, Indonesia) of Laius baliensis sp. nov. and L. satoi Yoshitomi, 2008, three Laius species living sympatrically. B. L. baliensis sp. nov., female. C. L. satoi, male. D. L. asahinai Nakane, 1955 (at Miyake-jima). Photographs by HY.
Fig. 11 in Comparative morphology of the endophallic structures of the genus Laius (Coleoptera, Melyridae), with the descriptions of three new species
Fig. 11. Larva of Laius rodriguesensis sp. nov. A. Maxillae and labium in ventral view. B. Labrum in dorsal (left) and ventral (right) views. C. Mandible in dorsal (left) and ventral (right) views.
Fig. 12 in Comparative morphology of the endophallic structures of the genus Laius (Coleoptera, Melyridae), with the descriptions of three new species
Fig. 12. Laius andamanensis sp. nov., ♂, paratype. A. Inner part of fore leg, showing enlarged femur and tibia. B. Antennomere III. C. Aedeagal apex. D. Spinous area (SEM photographs).
Fig. 8 in Comparative morphology of the endophallic structures of the genus Laius (Coleoptera, Melyridae), with the descriptions of three new species
Fig. 8. Male antennomere III of Laius spp. A. Laius baliensis sp. nov. (paratype). B. L. andamanensis sp. nov. (paratype). C. L. rodriguesensis sp. nov. (paratype). D. L. maai Wittmer, 1973 (paratype). E. L. marchei Pic, 1922. F. L. politus Fairmaire, 1880. G. L. sabangensis Wittmer, 1985 (paratype). H. L. sericatus Champion, 1924. I. L. submariniformis Wittmer, 1985 (paratype).
Fig. 5 in Comparative morphology of the endophallic structures of the genus Laius (Coleoptera, Melyridae), with the descriptions of three new species
Fig. 5. Dorsal habitus of Laius spp. of ♂ (holotypes A, C, E) and ♀♀ (paratypes B, D, F). A–B. Laius baliensis sp. nov. C–D. L. andamanensis sp. nov. E–F. L. rodriguesensis sp. nov. Scale bars = 1.0 mm.
Fig. 4 in Comparative morphology of the endophallic structures of the genus Laius (Coleoptera, Melyridae), with the descriptions of three new species
Fig. 4. Endophallic sclerites of Laius spp. A. Laius etsukoae Satô, Yoshitomi & Ohbayashi, 2006 (paratype). B. L. flavicornis (Fabricius, 1801). C. L. keiichii Satô, Yoshitomi & Ohbayashi, 2006 (paratype). D. L. lutaoensis Yoshitomi & Lee, 2010 (paratype). E. L. madli Yoshitomi, 2010 (paratype). F. L. miyamotoi Nakane, 1955. G. L. satoi Yoshitomi, 2008. H. L. taiwanus Yoshitomi & Lee, 2010 (paratype). I. L. pankowi Wittmer, 1999.
Fig. 6 in Comparative morphology of the endophallic structures of the genus Laius (Coleoptera, Melyridae), with the descriptions of three new species
Fig. 6. Dorsal habitus of Laius spp. (left: ♂; right: ♀). A. Laius maai Wittmer, 1973 (paratype). B. L. marchei Pic, 1922. C. L. politus Fairmaire, 1880. D. L. sabangensis Wittmer, 1985 (paratype). E. L. sericatus Champion, 1924. F. L. submariniformis Wittmer, 1985 (paratype). Scale bars = 1.0 mm.
Fig. 2 in Comparative morphology of the endophallic structures of the genus Laius (Coleoptera, Melyridae), with the descriptions of three new species
Fig. 2. Aedeagus of Laius lutaoensis Yoshitomi & Lee, 2010, showing the terminology and abbreviations for measurement of endophallic structures. A. Aedeagus with extracted endophallus. B. Aedeagus with holding endophallus (from Yoshitomi & Lee 2010). C. Gonoporal piece. D. Ligula.
Fig. 7 in Comparative morphology of the endophallic structures of the genus Laius (Coleoptera, Melyridae), with the descriptions of three new species
Fig. 7. Left antennae of Laius spp. (above: male; below: female). A. Laius baliensis sp. nov. (paratype). B. L. andamanensis sp. nov. (paratype). C. L. rodriguesensis sp. nov. (paratype). D. L. maai Wittmer, 1973 (paratype). E. L. marchei Pic, 1922. F. L. politus Fairmaire, 1880. G. L. sabangensis Wittmer, 1985 (paratype). H. L. sericatus Champion, 1924. I. L. submariniformis Wittmer, 1985 (paratype).
Fig. 1 in Comparative morphology of the endophallic structures of the genus Laius (Coleoptera, Melyridae), with the descriptions of three new species
Fig. 1. Copulation of Laius baliensis sp. nov. A. Endophallus fully engaged with female structures in dorsal view. B. Endophallus fully engaged with female structures in dorsal view, close up. Abbreviations: M = male, F = female.
Fig. 4 in Taxonomy and morphology of four "ophrys-related" scuticociliates (Protista, Ciliophora, Scuticociliatia), with the description of a new genus, Paramesanophrys gen. nov.
Fig. 4. Comparisons among different buccal apparatus patterns of Paramesanophrys gen. nov. and some related genera; arrows in A–J show different positions to which PM extends anteriorly and highlighted structures in A–J mark M2. A. Paramesanophrys typica gen. et sp. nov. (from the present work). B. Mesanophrys carcini (Grolière & Léglise, 1977) Small & Lynn in Aescht, 2001 (from Song & Wilbert 2000). C. Uronema marinum Dujardin, 1841 (from Song et al. 2009). D. Uronemella filificum (Kahl, 1931) Song & Wilbert, 2002 (from Song & Wilbert 2002). E. Metanophrys sinensis Song & Wilbert, 2000 (from Song & Wilbert 2000). F. Anophryoides haemophila Cawthorn et al., 1996 (from Cawthorn et al. 1996). G. Philasterides armatalis Song, 2000 (from Song 2000). H. Paranophrys marina Thompson & Berger, 1965 (from Song et al. 2002). I. Paralembus digitiformis Kahl, 1931 (from Song & Wilbert 2000). J. Cohnilembus verminus (Müller, 1786) Kahl, 1933 (from Song 2000). Abbreviations: M1–3 = membranelles 1, 2 and 3; PM = paroral membrane; Sc = scutica.
Fig. 7 in Taxonomy and morphology of four "ophrys-related" scuticociliates (Protista, Ciliophora, Scuticociliatia), with the description of a new genus, Paramesanophrys gen. nov.
Fig. 7. Metanophrys similis Song et al., 2002, in vivo (A–F) and after protargol staining (G–J). A. Ventral view of a typical individual. B–D. Ventral views of three individuals; arrowheads in D mark somatic cilia. E. Food vacuole (arrow). F. Posterior region; arrow shows caudal cilium. G, I. Ventral views, to show detailed structure of the buccal area. H. Dorsal view; arrow shows monokinetids, arrowhead marks dikinetids. J. Macronucleus. Abbreviations: M1–3 = membranelles 1, 2 and 3; Ma = macronucleus; PM = paroral membrane. Scale bars: A–D = 30 μm.
Fig. 6 in Taxonomy and morphology of four "ophrys-related" scuticociliates (Protista, Ciliophora, Scuticociliatia), with the description of a new genus, Paramesanophrys gen. nov.
Fig. 6. Metanophrys sinensis Song & Wilbert, 2000, in vivo (A–D, G) and after protargol (E–F, I–J) or silver nitrate (H) staining. A. Ventral view of a typical individual. B. Ventral view of another individual; arrowheads mark somatic cilia. C. Ventral view; arrowhead exhibits buccal field. D. Notched pellicle (arrowhead). E. Detailed structure of buccal area. F. Individual in morphogenesis, to show buccal apparatus. G. Ventral view, showing bar-shaped crystal (arrowhead). H. Detail of somatic kinetids. I. Dikinetids of scutica (arrowheads). J. Posterior region; arrowheads show monokinetids of somatic kineties. Abbreviations: M1–3 = membranelles 1, 2 and 3; PM = paroral membrane. Scale bars: A–B = 15 μm.
ScienceDex guides
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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.