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Figs 5–9 in Redescription of Omophoita octoguttata (Coleoptera: Chrysomelidae) and its immature stages, with notes on life history
Figs 5–9.Omophoita octoguttata (Fabricius, 1775), mouthparts of the adult: 5, labrum, frontal view; 6, left maxilla, dorsal view (I-V, maxillary palpomeres; LCN, lacinia; GLA, galea; BST, basistipe; DST, disistipe; CRD, cardo); 7, labium, ventral view (MNT, mentum; PRM, prementum; LGL, ligula); 8, 9, mandibles, frontal view: 8, right; 9, left (I-V, mandibular teeth; MSL, membranous setose lobe). Scale bar = 500 μm.
Figs 13–15 in Redescription of Omophoita octoguttata (Coleoptera: Chrysomelidae) and its immature stages, with notes on life history
Figs 13–15. Omophoita octoguttata (Fabricius, 1775), female genitalia: 13, tignum; 14, spermatheca; 15, vaginal palpi (RCP, receptacle; DCT, spermathecal duct). Scale = 200 μm.
Figs 10–12 in Redescription of Omophoita octoguttata (Coleoptera: Chrysomelidae) and its immature stages, with notes on life history
Figs 10–12. Omophoita octoguttata (Fabricius, 1775), male genitalia: 10, median lobe, dorsal view; 11, aedeagus, right lateral view; 12, detail of the apical hood of the median lobe, dorsal view (APH, apical hood; BHS, basal hooks; BOR, basal orifice; LTL, lateral lobes; MDL, middle lobe). Scale = 200 µm.
Figs 1–4 in Redescription of Omophoita octoguttata (Coleoptera: Chrysomelidae) and its immature stages, with notes on life history
Figs 1–4. Omophoita octoguttata (Fabricius, 1775). Dorsal habitus with color pattern variations: 1, female; 2, male. Frontal view of the head: 3, variant with rectangular maculae, female; 4, variant with rounded maculae, male.
Figs 7–18 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 7–18. Immature stages of Nisoniades macarius (Herrich-SchÄffer, 1870) in dorsal (left) and lateral (right) views: 7, 8, first instar larva; 9, 10, second instar larva; 11, 12, third instar larva; 13, 14, fourth instar larva; 15, 16, fifth instar larva; 17, 18, sixth instar larva.
Figs 28–31 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 28–31. TYpes of shelters built bY the larva of Nisoniades macarius (Herrich-SchÄffer, 1870) in Ipomoea asarifolia (Desr.) Roem. & Schult: 28, 29, TYpe 3 shelter, or center-cut shelters; 30, 31, TYpe 5 shelter, or two-cut shelters. The red arrows point to the shelter's location.
Figs 1, 2 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 1, 2. Collection area of the immatures of Nisoniades macarius (HerrichSchÄffer, 1870) (Fig. 1); the host plant of N. macarius, Ipomoea asarifolia (Desr.) Roem. & Schult. (Fig. 2).
Figs 32–36 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 32–36. Parasitoid of Nisoniades macarius (Herrich-SchÄffer, 1870) larva: 32, parasitized first instar larva; 33, parasitized third instar larva. Pupa of the parasitoid: 34, ventral view; 35, dorsal view. Fig. 36, parasitoid in adult form. The red arrows point to the parasitoid larvae.
Figs 3–6 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 3–6. Egg of Nisoniades macarius (Herrich-SchÄffer, 1870): 3, egg in the adaxial portion of the Ipomoea asarifolia (Desr.) Roem. & Schult. leaf; 4, egg in dorsal view; 5, egg in lateral view close to hatching; 6, egg after hatching.
Figs 19–27 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 19–27. Immatures and adults of Nisoniades macarius (Herrich-SchÄffer, 1870). Pre-pupa: 19, dorsal view; 20, lateral view. Pupa: 21, dorsal view; 22, lateral view; 23, ventral view; 24, frontal view. Fig. 25, adult female resting on grass leaf close to the host plant. Dorsal (left) and ventral (right) views of the adults raised in the laboratorY: 26, female; 27, male.
Figs 23-32 in Description of the postembryonic stages of Boeckella poopoensis (Crustacea, Copepoda, Centropagidae)
Figs 23-32. Abdomen, furcal setae and V pair of legs of Boeckella poopoensis copepodite stages. 23 to 25, furcal setae of copepodite I-III; 26, abdomen and furcal setae of copepodite IV; 27, V pair of legs of copepodite IV ♀; 28, V pair of legs of copepodite IV ♂; 29, abdomen and furcal setae of copepodite V ♀; 30, abdomen and furcal setae of copepodite V ♂; 31, V pair of legs of copepodite V ♀; 32, V pair of legs of copepodite V ♂ (ab, last abdominal segment; fb, furcal branch; cX, coXopod; bp, basipod; en, endopod; eX, eXopod).
Figs 1-22 in Description of the postembryonic stages of Boeckella poopoensis (Crustacea, Copepoda, Centropagidae)
Figs 1-22. Appendages of Boeckella poopoensis naupliar stages. 1, 4, 7, 10, 14 and 18, antennula of nauplius I-VI; 2, 5, 8, 11, 15 and 19, antenna of nauplius I-VI; 3, 6, 9, 12, 16 and 20, mandible of nauplius I-VI; 13, 17 and 21: maXillule of nauplius IV-VI; 22, maXilla of nauplius VI (s1, segment 1; s2, segment 2; s3, segment 3; cX, coXopod; bp, basipod; en, endopod; eX, eXopod; ilb, internal lobe; elb, eXternal lobe).
Fig. 1 in Effect of leaf decomposition stage and water temperature on fragmentation activity of a shredder invertebrate species in lotic ecosystems
Fig. 1. Schematic representation of the eXperimental design of the present study. EXperiment I: nine discs of senescent (S) and nine discs of conditioned senescent (SCD) wastes were used in each aquarium in the absence of shredder invertebrates. EXperiment II: nine discs of senescent (S), nine discs of conditioned senescent (SCD) and nine discs of green detritus (G) were used in each aquarium in the presence of shredded invertebrates (Phylloicus sp.).
Fig. 2 in Effect of leaf decomposition stage and water temperature on fragmentation activity of a shredder invertebrate species in lotic ecosystems
Fig. 2. Mean values and standard error of leaf mass loss (LML) of senescent (senescent plus conditioned senescent, due to the absence of visual distinction by coloration) and green detritus for larval case production by Phylloicus sp. in the different water temperature treatments at Capetinga Stream, Água Limpa Farm, Brasília, Brazil.
Fig. 5 in Ontogenetic stages of ceratopsian dinosaur Psittacosaurus in bone histology
Fig. 5. The skeletons of ceratopsian dinosaur Psittacosaurus lujiatunensis Zhou, Gao, Fox, and Chen, 2006 subadult (IVPP V14748, A; IVPP V18344, B) and adult P. lujiatunensis (IVPP V18343, C) from western Liaoning, China, Early Cretaceous.
Fig. 4 in Ontogenetic stages of ceratopsian dinosaur Psittacosaurus in bone histology
Fig. 4. Bone microstructure in juvenile ceratopsian dinosaur Psittacosaurus lujiatunensis Zhou, Gao, Fox, and Chen, 2006 from western Liaoning, China, Early Cretaceous. Mid-diaphyseal transverse section of right humerus (IVPP V14341.1, A), right radius (IVPP V14341.6, B), left tibia (IVPP V14341.5, C). Endosteal bone (arrow) showing in the inner most cortex and medullary cavity of right ulna (IVPP V14341.6, D), right radius (IVPP V14341.6, E), right femur (IVPP V14341.1, F), right fibula (IVPP V14341.1, G). Sharpey's fibres (arrows) in left tibia (IVPP V14341.5, H). Photographs in regular transmitted light (A1–C1, H1), elliptically polarized light (A2–C2, D, E, F, G, H2), line drawings (A3–C3) showing longitudinal vascular canals (navy), reticular vascular canals (green), radial vascular canals (red), and LAGs (brown lines). Abbreviation: ec, erosion cavity.
Fig. 1 in Ontogenetic stages of ceratopsian dinosaur Psittacosaurus in bone histology
Fig. 1. The cluster of hatchling ceratopsian dinosaur Psittacosaurus lujiatunensis Zhou, Gao, Fox, and Chen, 2006 (IVPP V16902) from western Liaoning, China, Early Cretaceous.
Fig. 2 in Ontogenetic stages of ceratopsian dinosaur Psittacosaurus in bone histology
Fig. 2. Bone microstructure in hatchling ceratopsian dinosaur Psittacosaurus lujiatunensis Zhou, Gao, Fox, and Chen, 2006 (IVPP V16902.1) from western Liaoning, China, Early Cretaceous. A–C. Mid-diaphyseal transverse section of tibia (A) and details (B, C); photographs in regular transmitted light (A1–C1), elliptically polarized light (A2–C2), crossed plane-polarized light (B3, C3). A3, line drawing showing longitudinal vascular canals (navy), reticular vascular canals (green) and radial vascular canals (red). Arrows indicate simple primary vascular canals.
Fig. 3 in Ontogenetic stages of ceratopsian dinosaur Psittacosaurus in bone histology
Fig. 3. Bone microstructure in juvenile ceratopsian dinosaur Psittacosaurus lujiatunensis Zhou, Gao, Fox, and Chen, 2006 (IVPP V14341.1) from western Liaoning, China, Early Cretaceous. A–C. Mid-diaphyseal transverse section of right tibia (A), the outer most cortex (B), the inner most cortex (C); photographs in regular transmitted light (A1–C1), elliptically polarized light (A2–C2), crossed plane-polarized light (B3, C3); line drawing (A3) showing longitudinal vascular canals (navy), reticular vascular canals (green), radial vascular canals (red), and LAGs (brown lines).
Fig. 6 in Ontogenetic stages of ceratopsian dinosaur Psittacosaurus in bone histology
Fig. 6. Bone microstructure in subadult ceratopsian dinosaur Psittacosaurus lujiatunensis Zhou, Gao, Fox, and Chen, 2006 from western Liaoning, China, Early Cretaceous. Mid-diaphyseal transverse section of right radius (IVPP V18344, A), left femur (IVPP V18344, B), left tibia (IVPP V14748, C), left fibula (IVPP V14748, D, E), left femur (IVPP 18344, F), left tibia (IVPP V18344, G). E–G show the endosteal bone (arrows). Photographs in regular transmitted light (A1–D1), elliptically polarized light (A2–D2, E–G); line drawings (A3–C3) showing longitudinal vascular canals (navy), reticular vascular canals (green), radial vascular canals (red), and LAGs (brown lines). Abbreviation: so, secondary osteons.
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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.