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Linked collectors and determiners for: Further Descriptions Of Western North American Podmosta Larvae And Their Separation From Ostrocerca Larvae (Plecoptera: Nemouridae).
Natural history specimen data linked to collectors and determiners held within, "Further Descriptions Of Western North American Podmosta Larvae And Their Separation From Ostrocerca Larvae (Plecoptera: Nemouridae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/3b644b6a-2a10-4153-9a6b-11ed35c7526e">https://bionomia.net/dataset/3b644b6a-2a10-4153-9a6b-11ed35c7526e</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/3b644b6a-2a10-4153-9a6b-11ed35c7526e">https://gbif.org/dataset/3b644b6a-2a10-4153-9a6b-11ed35c7526e</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Morphological and molecular evidence support the taxonomic separation of the medically important Neotropical spiders Phoneutria depilata (Strand, 1909) and P. boliviensis (F. O. Pickard-Cambridge, 1897) (Araneae, Ctenidae).
Natural history specimen data linked to collectors and determiners held within, "Morphological and molecular evidence support the taxonomic separation of the medically important Neotropical spiders Phoneutria depilata (Strand, 1909) and P. boliviensis (F. O. Pickard-Cambridge, 1897) (Araneae, Ctenidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/0a8bdd92-7bf8-44fb-8e8e-5c300df51a20">https://bionomia.net/dataset/0a8bdd92-7bf8-44fb-8e8e-5c300df51a20</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/0a8bdd92-7bf8-44fb-8e8e-5c300df51a20">https://gbif.org/dataset/0a8bdd92-7bf8-44fb-8e8e-5c300df51a20</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Morphological and molecular separation between Macrocamptoptera grangeri Soyka and M. metotarsa (Girault) (Hymenoptera: Mymaridae).
Natural history specimen data linked to collectors and determiners held within, "Morphological and molecular separation between Macrocamptoptera grangeri Soyka and M. metotarsa (Girault) (Hymenoptera: Mymaridae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/1de8c3eb-b3bc-40eb-9e86-a9f78a8f2161">https://bionomia.net/dataset/1de8c3eb-b3bc-40eb-9e86-a9f78a8f2161</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/1de8c3eb-b3bc-40eb-9e86-a9f78a8f2161">https://gbif.org/dataset/1de8c3eb-b3bc-40eb-9e86-a9f78a8f2161</a>. Formatted as a Frictionless Data package.
Figs 21–24 in Separation of Goniocotes Burmeister, 1838, and Dictyocotes Kéler, 1940 (Phthiraptera: Ischnocera), with descriptions of four new species
Figs 21–24. Comparison of gross morphology of Goniocotes Burmeister, 1838, and Dictyocotes Kéler, 1940. 21–22. G. gallinae (De Geer, 1778) (NHML). 21. Male. 22. Female. 23–24. D. rolandi (Gustafsson et al., 2021) (NHML). 23. Male. 24. Female.
Figs 18–20 in Separation of Goniocotes Burmeister, 1838, and Dictyocotes Kéler, 1940 (Phthiraptera: Ischnocera), with descriptions of four new species
Figs 18–20. Dictyocotes furcatus sp. nov. 18–19. Holotype, ♂ (BMNH, slide 29, box E0026136). 18. Head, dorsal and ventral views. 19. Genitalia, dorsal view. 20. Female genitalia, ventral view.
Figs 13–15 in Separation of Goniocotes Burmeister, 1838, and Dictyocotes Kéler, 1940 (Phthiraptera: Ischnocera), with descriptions of four new species
Figs 13–15. Goniocotes sarissa sp. nov. 13–14. Holotype, ♂ (BMNH, slide 95, box E0026011). 13. Head, dorsal and ventral views. 14. Genitalia, dorsal view. 15. Female genitalia, ventral view.
Fig. 16 in Separation of Goniocotes Burmeister, 1838, and Dictyocotes Kéler, 1940 (Phthiraptera: Ischnocera), with descriptions of four new species
Fig. 16. Dictyocotes furcatus sp. nov., holotype, ♂ (BMNH, slide 29, box E0026136). Habitus, dorsal and ventral views.
Fig. 11 in Separation of Goniocotes Burmeister, 1838, and Dictyocotes Kéler, 1940 (Phthiraptera: Ischnocera), with descriptions of four new species
Fig. 11. Goniocotes sarissa sp. nov., holotype, ♂ (BMNH, slide 95, box E0026011). Habitus, dorsal and ventral views.
Figs 8–10 in Separation of Goniocotes Burmeister, 1838, and Dictyocotes Kéler, 1940 (Phthiraptera: Ischnocera), with descriptions of four new species
Figs 8–10. Goniocotes cacumentalis sp. nov. 8–9. Holotype, ♂ (NHML, slide NHMUK010676049). 8. Head, dorsal and ventral views. 9. Genitalia, dorsal view. 10. Paratype, ♂ (NHML, slide NHMUK010676049). Genitalia, ventral view.
Figs 3–5 in Separation of Goniocotes Burmeister, 1838, and Dictyocotes Kéler, 1940 (Phthiraptera: Ischnocera), with descriptions of four new species
Figs 3–5. Goniocotes caoi sp. nov. 3–4. Holotype, ♂ (BMNH, slide 57, box E0026203). 3. Head, dorsal and ventral views. 4. Genitalia, dorsal view. 5. Female genitalia, ventral view. Abbreviations: as1–3 = anterior setae 1–3; avs1 = anterior ventral seta 1; dsms = dorsal submarginal seta; mts1–5 = marginal temporal setae 1–5; os = ocular seta; pns = postnodal seta; pos = preocular seta; pst = parameral seta; s1–6 = sensilla of dorsal head 1–6; vms = vulval marginal seta; vos = vulval oblique seta; vsms 1–2 = ventral submarginal setae 1–2; vss = vulval submarginal seta.
Fig. 7 in Separation of Goniocotes Burmeister, 1838, and Dictyocotes Kéler, 1940 (Phthiraptera: Ischnocera), with descriptions of four new species
Fig. 7. Goniocotes cacumentalis sp. nov., ♀ (NHML, slide NHMUK010676049). Habitus, dorsal and ventral views.
Fig. 1 in Separation of Goniocotes Burmeister, 1838, and Dictyocotes Kéler, 1940 (Phthiraptera: Ischnocera), with descriptions of four new species
Fig. 1. Goniocotes caoi sp. nov., holotype, ♂ (BMNH, slide 57, box E0026203). Habitus, dorsal and ventral views. Abbreviations: ipts = intermediate pteronotal seta; lpts = lateral pteronotal seta; mets = metathoracic seta; mss = mesothoracic seta; ppss = pronotal post-spiracular seta; ps = paratergal seta; psps = principal post-spiracular seta; ss = sutural seta; sts = sternal seta.
PLATE IVB. Metioche Stal, 1877. (A–G), Metioche japonica (Ichikawa, 2001): A, Eyes rounded, large and widely separated; B,Antennae: Scape and pedicel dark black, flagellum light in colour; C, Shape of last segment of maxillary palpi-securiform; D, Female sub-genital plate triangular; E, Male sub-genital plate; F, Male genitalia; G, Female ovipositor upturned, sabre shaped; apexsharp with teeth on ventre. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.
PLATE IVB. Metioche Stal, 1877. (A–G), Metioche japonica (Ichikawa, 2001): A, Eyes rounded, large and widely separated; B,Antennae: Scape and pedicel dark black, flagellum light in colour; C, Shape of last segment of maxillary palpi-securiform; D, Female sub-genital plate triangular; E, Male sub-genital plate; F, Male genitalia; G, Female ovipositor upturned, sabre shaped; apexsharp with teeth on ventre.
Cdt1 inhibits CMG helicase in early S phase to separate origin licensing from DNA synthesis
A fundamental concept in eukaryotic DNA replication is the temporal separation of G1 origin licensing from S phase origin firing. Re-replication and genome instability ensue if licensing occurs after DNA synthesis has started. In humans and other vertebrates, the E3 ubiquitin ligase CRL4Cdt2 starts to degrade the licensing factor Cdt1 after origins fire, raising the question of how cells prevent re-replication in early S phase. Here, using quantitative microscopy, we show that Cdt1 inhibits DNA synthesis during an overlap period when cells fire origins while Cdt1 is still present. Cdt1 inhibits DNA synthesis by suppressing CMG helicase progression at replication forks through the MCM-binding domain of Cdt1, and DNA synthesis commences once Cdt1 is degraded. Thus, instead of separating licensing from firing to prevent re-replication in early S phase, cells separate licensing from DNA synthesis through Cdt1-mediated inhibition of CMG helicase after firing.
Original Data for Manuscript "Energy and Momentum Distribution of Surface Plasmon-induced Hot Carriers Isolated via Spatiotemporal Separation"
<p>Raw data of the time-dependent energy density calculation and time-resolved photoemission electron microscopy (TR-PEEM) measurements used in the manuscript.</p> <p>A preprint of the manuscript is available on arXiv: <a href="https://arxiv.org/abs/2107.14277">2107.14277</a></p> <p>The manuscript was published in <em>ACS Nano</em> 2021, 15, 12, 19559-19569 <a href="https://doi.org/10.1021/acsnano.1c06586">10.1021/acsnano.1c06586</a></p> <p>The data is provided in hdf5 files, which were produced using the snomtools python package (<a href="https://github.com/hartelt/snomtools">availale on github</a>) and can be read with any <a href="https://support.hdfgroup.org/HDF5/tools5desc.html">hdf5 compatible software</a>. The calculated data was produced as described in Ref.1 with the parameters given in the manuscript. For the experimental data, each zip file contains the raw data (hdf5 Files) as well as the PEEM settings used (sav Files as output from the experiment control software) for the respective measurement.</p> <p>Parts of the manuscript that are generated from the calculated data [calculation_energy_density.zip]:</p> <ul> <li>Figure 2 A</li> <li>Figure S2</li> </ul> <p>Parts of the manuscript that are evaluated from the PEEM real space dataset [PEEM_realspace.zip]:</p> <ul> <li>Figure 2 B</li> <li>Figure 3</li> <li>Figure S1</li> <li>Figure S3</li> <li>Figure S4</li> <li>Movie S2 [timeseries_binned_fermi.avi] in the supplementary material</li> </ul> <p>Parts of the manuscript that are evaluated from the PEEM momentum space (momentum microscopy) SPP dataset [PEEM_k-space_timesteps_SPP.zip]:</p> <ul> <li>Figure 4 (in combination with the pump pulse reference dataset)</li> <li>Figure S5 B</li> <li>Figure S6 B</li> <li>Figure S7 B</li> </ul> <p>Parts of the manuscript that are evaluated from the PEEM momentum space (momentum microscopy) pump pulse reference dataset [PEEM_k-space_timesteps_pump.zip]:</p> <ul> <li>Figure 4 (in combination with the SPP dataset)</li> <li>Figure S5 A</li> <li>Figure S6 A</li> <li>Figure S7 A</li> </ul> <p>Parts of the manuscript that are evaluated from the PEEM momentum space (momentum microscopy) data of the full timetrace, combining SPP dataset [PEEM_k-space_full-timetrace_SPP.zip] and pump pulse reference dataset [PEEM_k-space_full-timetrace_pump.zip]:</p> <ul> <li>Figure S8</li> </ul>
Explanation of Plate I. Figure 1.—Left tibia of Ornithomimus velox, Marsh; A, front view; b, distal end; c, transverse section. Figure 2.—Left metatarsals of same specimen; A, front view; b, proximal ends; c, transverse section; d, distal ends. Figure 3.—Phalanges of second digit of same foot; front view, a, first phalange; b, second phalange; c, third, or terminal phalange. Figure 4.—Left metacarpals of same species, perhaps of smaller individual; front view. Figure 5.—Left tibia of young Ostrich (Struthio camelus, Linn.); a, front view; b, distal end. The separate calcaneum was first observed by the writer's assistant, Dr. G-. Baur, who prepared the specimen. Figure 6.—Left metatarsals of young turkey (Meleagris gallipavo, Linn.); a, front view; b, proximal ends. a, astragalus; as, ascending process of astragalus; c, calcaneum; f, fibula; f' face for fibula; II, second metatarsal; III, third metatarsal; iv, fourth metatarsal. Figures 1-4 are one-third natural size, and figures 5 and 6, one-half natural size. in Description of new dinosaurian reptiles
Explanation of Plate I. Figure 1.—Left tibia of Ornithomimus velox, Marsh; A, front view; b, distal end; c, transverse section. Figure 2.—Left metatarsals of same specimen; A, front view; b, proximal ends; c, transverse section; d, distal ends. Figure 3.—Phalanges of second digit of same foot; front view, a, first phalange; b, second phalange; c, third, or terminal phalange. Figure 4.—Left metacarpals of same species, perhaps of smaller individual; front view. Figure 5.—Left tibia of young Ostrich (Struthio camelus, Linn.); a, front view; b, distal end. The separate calcaneum was first observed by the writer's assistant, Dr. G-. Baur, who prepared the specimen. Figure 6.—Left metatarsals of young turkey (Meleagris gallipavo, Linn.); a, front view; b, proximal ends. a, astragalus; as, ascending process of astragalus; c, calcaneum; f, fibula; f' face for fibula; II, second metatarsal; III, third metatarsal; iv, fourth metatarsal. Figures 1-4 are one-third natural size, and figures 5 and 6, one-half natural size.
Comet C/2020F3 (Neowise) with separate dust and ion gas tails and a green glowing coma, by Dietmar Gutermuth, Germany
<p>Second place in the 2021 IAU OAE Astrophotography Contest, category Comets.</p> <p>Comets have a very interesting structure comprising of four main parts: the nucleus, composed of rock, dust and frozen gases, typically spanning a few kilometres, although bigger ones have been observed; a small atmosphere of gas surrounding the nucleus (only present when the comet approaches its closest point to the Sun), called coma; and the two distinctive cometary tails (there is at times third tail). The green colour of the coma is due to carbon and nitrogen present in the coma reacting with the Sun’s ultraviolet radiation. The tail that we are mostly used to observing – dust tail and is composed of micron sized dust particles, the second tail composed of charged particles – ion or gas tail. The tails are released only when the comet approaches the Sun at a distance where the heat and radiation emanating from our star is intense enough to vaporize the frozen gases. The dust tail is curved, while the gas tail is straight and always points away from the Sun as this is carried by the solar wind - flow of charged particles emitted by the Sun. As comets are formed by leftover material, they carry with them important information about the early stages of the Solar System’s formation. This beautiful image shows the comet C/2020 F3 (Neowise), as seen from Germany in July 2020, with three of the four structures clearly visible – coma, gas, and dust tail.</p> <p>Credit:<strong> </strong>Dietmar Gutermuth/IAU OAE</p>
Fig. 24 in Phylogenetic Studies On Didelphid Marsupials Ii. Nonmolecular Data And New Irbp Sequences: Separate And Combined Analyses Of Didelphine Relationships With Denser Taxon Sampling
Fig. 24. Tlacuatzin canescens, photographed by Gerardo Ceballos in March 1995 at the ChamelaCuixmala Biosphere Reserve, Jalisco, Mexico. Specimens from southern populations (especially topotypical material from Oaxaca) are markedly grayer than this individual.
Fig. 12 in Phylogenetic Studies On Didelphid Marsupials Ii. Nonmolecular Data And New Irbp Sequences: Separate And Combined Analyses Of Didelphine Relationships With Denser Taxon Sampling
Fig. 12. Bivariate comparison of two dental proportions discussed in the text, with illustrated examples of contrasting morphologies. Closed curves delimit sets of taxa assigned to alternative states of character 57. Taxon labels: 1, Caluromys lanatus; 2, Caluromys philander; 3, Caluromysiops irrupta; 4, Chironectes minimus; 5, Didelphis albiventris; 6, Didelphis marsupialis; 7, Didelphis virginiana; 8, Glironia venusta; 9, Gracilinanus microtarsus; 10, Lestodelphys halli; 11, Lutreolina crassicaudata; 12, Marmosa canescens; 13, Marmosa lepida; 14, Marmosa mexicana; 15, Marmosa murina; 16, Marmosa robinsoni; 17, Marmosa rubra; 18, Marmosops impavidus; 19, Marmosops incanus; 20, Marmosops noctivagus; 21, Marmosops parvidens; 22, Marmosops pinheiroi; 23, Metachirus nudicaudatus; 24, Micoureus demerarae; 25, Micoureus paraguayanus; 26, Micoureus regina; 27, Monodelphis adusta; 28, Monodelphis brevicaudata; 29, Monodelphis emiliae; 30, Monodelphis theresa; 31, Philander frenata; 32, Philander mcilhennyi; 33, Philander opossum; 34, Thylamys pallidior; 35, Thylamys venustus. Other labels: MC, metacrista; PC, postprotocrista.
Fig. 20 in Phylogenetic Studies On Didelphid Marsupials Ii. Nonmolecular Data And New Irbp Sequences: Separate And Combined Analyses Of Didelphine Relationships With Denser Taxon Sampling
Fig. 20. Strict consensus of 18 maximumlikelihood trees under the bestfit model of IRBP sequence evolution, rooted to be consistent with our assumption of ingroup (didelphine) monophyly (see text). Bootstrap support values are shown below each branch. Outgroup taxa are indicated with asterisks.
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.