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FIGURE 37. Stage 2 in Observations on the biology of Afro-tropical Hesperiidae (Lepidoptera) principally from Kenya. Part 1. Introduction and Coeliadinae
FIGURE 37. Stage 2 leaf shelters of Coeliades sejuncta, which contained instar 3 caterpillars, collected on Triaspis mozambica, Diani Beach, 21 Aug 1995 (95/105).
FIGURE 14. Stage 3 in Observations on the biology of Afro-tropical Hesperiidae (Lepidoptera) principally from Kenya. Part 1. Introduction and Coeliadinae
FIGURE 14. Stage 3 leaf shelter of Coeliades chalybe on Acridocarpus longifolius, Adiopodoumé, Côte d'Ivoire; left, closed shelter; right, open shelter with penultimate instar caterpillar; 6 Dec 1988 (88/211).
Water stages in a tidal marsh measured using images, visually and automatically, along with stages measured using pressure transducer and Doppler sensors
<p>This data was acquired to evaluate the performance of an image based system to measure water stages in streams and rivers.</p> <p>It contains measurements performed visually and stored (NR_Visual_Data_120201_120724.csv)</p> <p>It contains the measurements performed automatically by the system studied corresponding to those done visually (NR_Gaugecam_Data_120201_120724.csv)</p> <p>It contains the measurements done automatically (GC) and those measured by ISCO, HOBO, and Sontek instruments (NR-GC-vs-ISCO.csv)</p>
FIGURE. Seedlings, seeds, embryos, anthers, and pollen in Dicorynia. A–D. Different stages of development in seedlings of D. paraensis, First eophiles unifoliolate and opposite; E–G. Seed of D. guianensis: E. External surface; F. Endosperm of the longitudinally sectioned seed, note the slightly gelatinous upper region; G. Cotyledon and embryo of longitudinally sectioned seed; H. SEM of seed's testa in D. paraensis; I. SEM of endosperm's surface in D. guianensis (notice the presence of circular perforations); J–K. SEM of the hypocotyl-radicular axis of the seed in D. guianensis and D. paraensis; L. SEM of seed's testa in D. guianensis; M–N. SEM of plumule region in embryo of D. guianensis and D. paraensis (note the developed leaf primordia); O. Apex of anther in longer stamen of D. paraensis, showing 4 sporangia and two pores covered by an apicle; P. Apex of anther in shorter stamen of D. guianensis, at least 9 sporangia; Q. Apex of anther in longer stamen of D. guianensis, 8 sporangia; R. Pollen grains in D. paraensis. A–D: Falcão, M.J. 91; E–G, I–J, L–M: Gentry 63030; H, K, N: Berry, P.E. 7460; O: Amaral, E. 618; P, Q: Unknown collector MO1576407; Scale bar. A–D: 2cm; E–G: 3mm; H–L: 1mm; M–N: 100 μm; O-Q: 200μm; R: 5 μm. in A Taxonomic Revision of the Amazonian Genus Dicorynia (Fabaceae: Dialioideae)
FIGURE. Seedlings, seeds, embryos, anthers, and pollen in Dicorynia. A–D. Different stages of development in seedlings of D. paraensis, First eophiles unifoliolate and opposite; E–G. Seed of D. guianensis: E. External surface; F. Endosperm of the longitudinally sectioned seed, note the slightly gelatinous upper region; G. Cotyledon and embryo of longitudinally sectioned seed; H. SEM of seed's testa in D. paraensis; I. SEM of endosperm's surface in D. guianensis (notice the presence of circular perforations); J–K. SEM of the hypocotyl-radicular axis of the seed in D. guianensis and D. paraensis; L. SEM of seed's testa in D. guianensis; M–N. SEM of plumule region in embryo of D. guianensis and D. paraensis (note the developed leaf primordia); O. Apex of anther in longer stamen of D. paraensis, showing 4 sporangia and two pores covered by an apicle; P. Apex of anther in shorter stamen of D. guianensis, at least 9 sporangia; Q. Apex of anther in longer stamen of D. guianensis, 8 sporangia; R. Pollen grains in D. paraensis. A–D: Falcão, M.J. 91; E–G, I–J, L–M: Gentry 63030; H, K, N: Berry, P.E. 7460; O: Amaral, E. 618; P, Q: Unknown collector MO1576407; Scale bar. A–D: 2cm; E–G: 3mm; H–L: 1mm; M–N: 100 μm; O-Q: 200μm; R: 5 μm.
Direct tailpipe measurements of δ15N-NH3 at different emission stages
<p>Vehicle details, NH<sub>3</sub> concentrations and <em>δ</em><sup>15</sup>N-NH<sub>3</sub> values for collected exhaust samples (triplicate).</p>
STED immunofluorescence imaging of histone protein H3K27 in a 2-cell stage mice embryo
<p>In either confocal or STED mode, immunofluorescence was performed as previously described in [1], using an upright Zeiss microscope with a mounted STEDYCON module and a Zeiss 100x 1.46 NA objective. Primary antibodies used were anti-H3K27ac (Active Motif, 39034) and anti-H3K27me3 (Abcam, ab6002), both at 1:200 dilution. Secondary anti-mouse and anti-rabbit antibodies used were labeled with STAR Red (Sigma-Aldrich, 52283) and STAR Orange (Sigma-Aldrich, 41367), respectively. Excitation was provided by 640 nm (@3%) and 775 nm (@96.5%) lasers for the STAR Red channel, whereas 561 nm (@7.8%) and 775 nm (@100%) lasers were used for the STAR Orange channel. Imaging of the samples was performed with 5 µs pixel dwell time, 64 µm pinhole aperture, 15-line accumulations and a pixel size of 20 nm.</p> <p>Experimental procedures were approved by the EMBL Rome Animal Facility in accordance with European and Italian legislations.</p> <p>1. Bošković, A., Bender, A., Gall, L., Ziegler-Birling, C., Beaujean, N., & Torres-Padilla, M.-E. Analysis of active chromatin modifications in early mammalian embryos reveals uncoupling of h2a.z acetylation and h3k36 trimethylation from embryonic genome activation. Epigenetics 7, 747–757 (2012).</p>
Coriander fruits different developmental stages NMR raw data
<p>Coriander fruits at different developmental stages NMR raw data</p>
FIGURE 1. Tetraxanthus rathbunae Chace, 1939. Zoea I. a in The first zoeal stage of the deep-sea crab Tetraxanthus rathbunae (Brachyura Pseudorhombilidae): a morphological description
FIGURE 1. Tetraxanthus rathbunae Chace, 1939. Zoea I. a, lateral view; b, abdomen dorsal view; c, antennule; d, antenna; e, antenna exopod; f, mandible; g, maxillule; h, maxilla; i, first maxilliped; j, second maxilliped; k, telson. Scale bars: a = 0.5 mm; b = 0.2 mm; d, f, i–k = 0.1 mm; c, g, h = 0.05 mm; e = 0.01 mm.
FIGURE 2. Stage 41 in Description of two dendrobatid tadpoles (Anura: Dendrobatidae: Andinobates and Oophaga) with comments on egg clutches
FIGURE 2. Stage 41 tadpoles of (a) preserved Andinobates geminisae and (b) live Oophaga vicentei and ≤ 3 Stage eggs of (c) A. geminisae and (d) O. vicentei. Scale bars = 10 mm (a,b) and 5 mm (c,d).
Life stage and taxonomy the most important factors determining vertebrate stoichiometry: A meta-analysis
<p>1. Whole-body elemental composition is a key trait for determining how organisms influence their ecosystems. Using mass-balance, ecological stoichiometry predicts that animals with higher concentrations of element X will selectively retain more X and will recycle less X in their waste than animals with lower X concentrations. These animals will also store high quantities of X during their lives and after their deaths (prior to full decomposition).</p> <p>2. Vertebrates may uniquely impact nutrient cycling because they store high quantities of phosphorus (P) in their bones. However, vertebrates have diverse body forms and invest variably in bone. Current analyses of vertebrate elemental content predominately evaluate fishes, typically neglecting other vertebrates and leaving much of the diversity unexplored.</p> <p>3. We performed a systematic review and identified 179 measurements of whole-body percent phosphorus (%P), percent nitrogen (%N), and N to P ratio (N:P) from 129 unique species of non-fish vertebrates (amphibians: 39 species; reptiles: 19 species; birds: 27 species; mammals: 46 species)</p> <p>4. We found that %P (mean: 1.94%; sd (standard deviation) = 0.77) and N:P (mean: 12.52) varied with taxonomy and life stage, while %N (mean: 10.51%; sd = 3.25) varied primarily with taxonomy. Habitat, diet, and size had small and inconsistent effects in different groups.</p> <p>5. Our study highlights two research gaps. Life stage, which is frequently neglected in stoichiometric studies, is an important factor determining vertebrate %P. Furthermore, amphibians dominate our dataset, while other vertebrate taxa are poorly represented in the current literature. Further research into these neglected vertebrate taxa is essential.</p>
FIGURES 37–40. Foreleg. 37, 38 in Descriptions of the developmental stages of Cafius nauticus (Fairmaire) (Coleoptera: Staphylinidae: Staphylininae), with comments on its biology
FIGURES 37–40. Foreleg. 37, 38. First larval instar; 39. Second larval instar; 40. Third larva instar; 38. Seta on tarsungulus. Abbreviations: 1–31=setae, a–d=pores, CX=coxa, FE=femur, TB=tibia, TR=trochanter, TU=tarsungulus.
FIGURES 75–80. Adult. 75–76 in Descriptions of the developmental stages of Cafius nauticus (Fairmaire) (Coleoptera: Staphylinidae: Staphylininae), with comments on its biology
FIGURES 75–80. Adult. 75–76. Habitus of Cafius nauticus in dorsal (75), ventral (76) aspect; 77–78. Aedeagus, lateral (77) and ventral (78) views; 79. Male abdominal tergite X. 79. Male abdominal sternite IX.
FIGURES 24–27. Antenna. 24–26 in Descriptions of the developmental stages of Cafius nauticus (Fairmaire) (Coleoptera: Staphylinidae: Staphylininae), with comments on its biology
FIGURES 24–27. Antenna. 24–26. First larval instar; 27. Third larval instar; 24, 27. General appearance in dorsal aspect; 25. Apex of antennal article IV; 26. Region of sensory appendage of antennal article III. Abbreviations: 1–6=setae, a–d=pores, SA=sensory appendage, SO=solenidia.
FIGURES 19–23. First larval instar 19. Nasale, 20. Mandible, 21–23. Epipharynx. 21 in Descriptions of the developmental stages of Cafius nauticus (Fairmaire) (Coleoptera: Staphylinidae: Staphylininae), with comments on its biology
FIGURES 19–23. First larval instar 19. Nasale, 20. Mandible, 21–23. Epipharynx. 21. Olfactory organs; 22. General appearance; 23. Long cuticular processes posteriorly. Abbreviations: 1–2=setae, a–b=pores, LT=lateral tooth, MT=median tooth, OG=olfactory organ, PMT=paramedian tooth.
FIGURES 52–59. Abdomen. 52–54, 58–59 in Descriptions of the developmental stages of Cafius nauticus (Fairmaire) (Coleoptera: Staphylinidae: Staphylininae), with comments on its biology
FIGURES 52–59. Abdomen. 52–54, 58–59. First larval instar; 52. Abdominal tergites I and II; 53. Abdominal sternites I and II; 54. Fused paratergite and parasternite of abdominal segment I and II; 58. Spiracle; 59. Microstructure of abdominal tergite III; 55–57. Third larva instar; 55. Abdominal tergites I and II; 56. Abdominal sternites I and II; 57. Fused paratergite and parasternite of abdominal segment I and II. Abbreviations: 1–21=setae, a–d=pores, PS=parasternite, PT=paratergite, PTG=pretergal gland, S=sternite, SP=spiracle, T=tergite.
FIGURES 28–32. Maxilla. 28–31 in Descriptions of the developmental stages of Cafius nauticus (Fairmaire) (Coleoptera: Staphylinidae: Staphylininae), with comments on its biology
FIGURES 28–32. Maxilla. 28–31. First larval instar; 32. Third larval instar; 28, 32. General appearance in dorsal aspect; 29. Apex portion of maxillary palp; 30. Region of digitiform sensory appendage of maxillary palp III; 31. Region of mala. Abbreviations: 1–11=setae, a–g=pores, CD=cardo, DSA=digitiform sensory appendage, MA=mala, PF=palpifer, SO=solenidia, ST=stipes.
FIGURES 13–18. Head. 13–17 in Descriptions of the developmental stages of Cafius nauticus (Fairmaire) (Coleoptera: Staphylinidae: Staphylininae), with comments on its biology
FIGURES 13–18. Head. 13–17. First larval instar; 13. Head in dorsal aspect; 14. Head in ventral aspect; 15–16. Seta on head; 17. Ventral tentorial pit; 18. Head of third larva instar in dorsal aspect. Abbreviations: 1–39=setae, a–k=pores, AP=apotome, E=epicranial part, EG=epicranial gland, GP=glandular pit, NA=nasale, P=posterior part, VTP=ventral tentorial pit.
FIGURES 68–74. Pupa. 68–70 in Descriptions of the developmental stages of Cafius nauticus (Fairmaire) (Coleoptera: Staphylinidae: Staphylininae), with comments on its biology
FIGURES 68–74. Pupa. 68–70. Habitus of pupa in dorsal (68), ventral (69) and lateral (70) aspect; 71–72. Microstructure of setiform projections on anterior margin of pronotum; 73–74. Microstructure of setiform projections on abdomen. Abbreviations: VP= ventral prolongations, FSP= functional spiracles, ASP= atrophied spiracles.
FIGURES 60–67. Abdominal segment IX, X and urogomphus. 60–62, 66–67 in Descriptions of the developmental stages of Cafius nauticus (Fairmaire) (Coleoptera: Staphylinidae: Staphylininae), with comments on its biology
FIGURES 60–67. Abdominal segment IX, X and urogomphus. 60–62, 66–67. First larval instar; 60. Abdominal segment IX and X, dorsal aspect; 61. Abdominal segment IX and X, ventral aspect; 62, 66. Urogomphus; 67. Microstructure of abdominal tergite X; 63–65. Mature larva instar; 63. Abdominal segment IX and X, dorsal aspect; 64. Abdominal segment IX and X, ventral aspect; 65. Urogomphus. Abbreviations: 1–30=setae, a–c=pores.
FIGURES 41–51. Thorax. 41–50 in Descriptions of the developmental stages of Cafius nauticus (Fairmaire) (Coleoptera: Staphylinidae: Staphylininae), with comments on its biology
FIGURES 41–51. Thorax. 41–50. First larval instar; 51. Third larval instar; 41, 51. Thorax in dorsal aspect; 42. Thorax in ventral aspect; 43–50. Seta on pronotum and abdominal tergite. Abbreviations: 1–27=setae, a–f=pores, CS=cervicosternum, ES=episternum, SP=spiracle.
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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.