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209 results for “confocal microscopy”
FIGURE 5 in Oziella sibirica (Acari: Eriophyoidea: Phytoptidae), a new eriophyoid mite species described using confocal microscopy, COI barcoding and 3 D surface reconstruction
FIGURE 5. Oziella sibirica sp. nov., larva. A. Ventral view; B. Prodorsal shield and anterior part of opisthosoma; C. Coxisternal area and anteroventral region of opisthosoma; D. Right leg I, dorsal view; E. Right leg II, dorsal view; F. Typical 4/3-rayed empodium. Scale bar: A = 100; B & C = 45; D & E = 35; F = 10.
FIGURE 1 in Re-description of Craspodema reflectans (Nematoda, Cyatholaimidae) using confocal laser scanning microscopy
FIGURE 1. Male specimen of Craspodema reflectans collected in Maldives during the 2009 scientific cruise. A) Habitus; B) Cervical region; C) Detail of the amphideal fovea and cuticular ornamentation; D) Detail of the buccal cavity; E) Detail of the copulatory apparatus; F) View of the precloacal supplements. Scale bars: A = 100µm; B–E = 10µm; F = 30 µm.
FIGURE 4 in Re-description of Craspodema reflectans (Nematoda, Cyatholaimidae) using confocal laser scanning microscopy
FIGURE 4. Light micrographs of a female of Craspodema reflectans A) View of the dorsal tooth in the buccal cavity; B) View of the ventral teeth; C) Detail of the amphideal fovea; D) Mid-body region showing vulva. Scale bars: A–D = 5 µm.
FIGURE 6 in Re-description of Craspodema reflectans (Nematoda, Cyatholaimidae) using confocal laser scanning microscopy
FIGURE 6. Light micrographs of Craspodema octogoniata male. A) Detail of the amphideal fovea; B) Detail of the dorsal tooth; C) View of the ventral teeth; D) Detail of the cuticular ornamentation in the middle of the body; E) Precloacal supplements; F) Detail of the copulatory apparatus. Scale bars: A–C = 5µm; D = 10µm; E,F = 10µm.
FIGURE 3 in Re-description of Craspodema reflectans (Nematoda, Cyatholaimidae) using confocal laser scanning microscopy
FIGURE 3. Female specimen of Craspodema reflectans. A) Habitus; B) Detail of the amphideal fovea; C) Detail of the buccal cavity. Scale bars: A = 100µm; B,C = 10 µm.
FIGURE 7 in Re-description of Craspodema reflectans (Nematoda, Cyatholaimidae) using confocal laser scanning microscopy
FIGURE 7. Confocal laser scanning micrograph of Craspodema octogoniata male. A) Detail of the amphideal fovea; B) Reconstruction of the cephalic region of a male and detail of the rugae; C) Reconstruction of the buccal cavity; D) Reconstruction of the copulatory apparatus. Scale bars: A–D = 5 µm.
FIGURE 2 in Re-description of Craspodema reflectans (Nematoda, Cyatholaimidae) using confocal laser scanning microscopy
FIGURE 2. Light micrographs of a male of Craspodema reflectans. A) Detail of the buccal cavity; B) Detail of the amphideal fovea; C–D) cuticular ornamentation of the middle part of the body and cervical region; E) Precloacal supplements and gubernaculum structure; F) Detail of the copulatory apparatus. Scale bars: A = 5µm; B–F = 10 µm.
FIGURE 5 in Re-description of Craspodema reflectans (Nematoda, Cyatholaimidae) using confocal laser scanning microscopy
FIGURE 5. Confocal laser scanning micrograph of Craspodema reflectans. A) Reconstruction of the cephalic region of a male and detail of the eversible rugae; B) Reconstruction of the buccal cavity of a male; C) View of the male amphideal fovea; D) View of the female amphideal fovea; E) View of the precloacal supplements region; F) Reconstruction of the copulatory apparatus. Scale bars: A = 5 µm; B–F = 10 µm.
FIGURE 6. 3D in Confocal laser scanning microscopy technique for the study of internal genitalia and external morphology of eriophyoid mites (Acari: Eriophyoidea)
FIGURE 6. 3D-reconstruction of the internal genitalia of Phytoptus rigidus, bottom view (the same female as Fig. 2A). A. spermathecae, B. spherical spermathecal tube, C. capsule-like reservoir in the connection of two spermathecal tubes, D. transversal genital apodeme, E. distal folder of transversal genital apodeme, F. longitudinal genital? apodeme1 (includes two sclerotised plates), G. epigynium.
FIGURE 8 in Confocal laser scanning microscopy technique for the study of internal genitalia and external morphology of eriophyoid mites (Acari: Eriophyoidea)
FIGURE 8. CLSM images of eriophyoid mites using reflected red laser (wavelength emission range of 627–637 nm). A. empodia and leg setae of Phytoptus?tetratrichus; B. empodia and leg setae of P. atherodes; C. gnathosomal stylets of Phytoptus chamaebatiae; D. antero-ventral aspect of Setoptus pini; E. antero-ventral aspect of Oziella sp.; F. prodorsal shield of Boczekella reticulata. Note: the colour was changed from red (original pseudo-colour) to white (A, C, E, F) and to light blue (B) to increase contrast.
FIGURE 3 in Confocal laser scanning microscopy technique for the study of internal genitalia and external morphology of eriophyoid mites (Acari: Eriophyoidea)
FIGURE 3. Images obtained via LSCM of specimens on older microscope slides. A. Boczekella reticulata (slide-mounted on 11 May 2010); B. Sierraphytoptus ambulans (21 Sept. 2008), C. Phytoptus atherodes (5 Aug. 2003), D. Novophytoptus?stipae (9–14 Sept. 1976, uncoloured and black-white inverted). Note: empodia and proximal part of setae are not visible with blue laser (see 2B & 2D).
FIGURE 5 in Confocal laser scanning microscopy technique for the study of internal genitalia and external morphology of eriophyoid mites (Acari: Eriophyoidea)
FIGURE 5. CLSM images (blue laser) of female internal genitalia (A) and spermatophore inside male (B). A. Phytoptus chamaebatiae. B. Setoptus pini. Note: original pseudocolour obtained from CLS microscope using Leica software was saved on both images.
FIGURE 2 in Confocal laser scanning microscopy technique for the study of internal genitalia and external morphology of eriophyoid mites (Acari: Eriophyoidea)
FIGURE 2. Larvae of Phytoptus hirtae inside egg (fresh microscope slides). Note: the colour was changed from original (pseudo colour) red to light blue-green for enhancing contrast.
FIGURE 1 in Confocal laser scanning microscopy technique for the study of internal genitalia and external morphology of eriophyoid mites (Acari: Eriophyoidea)
FIGURE 1. Images obtained via CLSM of fresh microscope slides (specimens mounted between April and September 2011). A. Phytoptus rigidus; B. Trisetacus?kirghisorum; C. Setoptus pini. Original colour (pseudo-colour) kept. Note: blue is the colour of the exciting laser.
FIGURE 7 in Confocal laser scanning microscopy technique for the study of internal genitalia and external morphology of eriophyoid mites (Acari: Eriophyoidea)
FIGURE 7. CLSM images of empodia of Setoptus pini (reflected laser light): A. red laser, B. blue laser, C. green laser. Note: the original pseudo-colour was changed to red (A), blue (B) and green (C).
Dataset for 'Comparison of coherence scanning interferometry, focus variation and confocal microscopy for surface topography measurement'
<p>The original measurement data shown in Figures 1 to 3 of the Euspen conference publication: Comparison of coherence scanning interferometry, focus variation and confocal microscopy for surface topography measurement, https://www.euspen.eu/knowledge-base/ICE23170.pdf. </p><p><strong>Acknowledgements </strong></p><p>The authors would like to thank the UKRI Research England Development (RED) Fund for funding this work via the Midlands Centre for Data-Drive Metrology. This work was supported by the European Metrology Programme for Innovation and Research (EMPIR) project (TracOptic, 20IND07) and the European Union (ERC, AI-SURF, 101054454).</p>
Data and visualisation code from 'Effects and avoidance of photoconversion-induced artefacts in confocal and STED microscopy' by Dasgupta et al (2024)
Open the record for dataset details and reuse information.
FIGURE 1 in Micromorphology of seeds of three Mexican species of Pinguicula (Lentibulariaceae) show autofluorescence using confocal laser scanning microscopy
FIGURE 1. Confocal laser scanning microscopy images showing the micromorphological features of Pinguicula seeds. A–D. Pinguicula casperi; E–H. P. parvifolia; I–L. P. oblongiloba. A, E and I are a general view of the entire seeds (20×, scale bar 100 μm); B, F and J show the micropylar end (60×, scale bar 20 μm); D, H, and L show the chalazal end of the seed (60×, scale bar 20 μm); C, G and K show the surface details of the seeds (100×, scale bar 10 μm).
Hyperspectral Multipoint High-Speed Confocal Microscopy Supporting Information Movies
<p><strong>S1 Movie. Neuronal growth in a zebrafish embryo</strong>. Sensory neurons (green) are labeled with GFP and motor neurons (magenta) are labelled with mCherry. The video was captured with filter configuration 2 (see section "System Dichroics and Emission Filters") frames were taken every minute.</p> <p> </p><p><strong>S2 Movie. Video of mitosis in a live <em>Xenopus laevis</em> embryo.</strong> The cellular membranes (magenta) is labelled with mTagBFP::CAAX; chromatin (blue) is labelled with miRFP670::H2B; and mitotic spindles (green) are labelled with mCherry:α-tubulin. One frame of 75 ms exposure time was captured every 5 seconds. The video was captured with filter configuration 2 (see section "System Dichroics and Emission Filters").</p> <p></p>
Fig. 2 Confocal laser scanning microscopy images showing the hard tick morphology. a in parasitised feathered dinosaurs as Cretaceous amber assemblages revealed
Fig. 2 Confocal laser scanning microscopy images showing the hard tick morphology. a Habitus in ventral view of the Cornupalpatum burmanicum nymph associated with feathers. Scale bar, 0.2 mm. b Detail of the gnathosoma and coxal area in ventral view revealing the absence of genital pore. Scale bar, 0.1 mm. c Dorsal view detail of the gnathosoma and anterior part of the scutum (arrow indicates the lateral margin of the scutum). Scale bar, 0.1 mm
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.