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Figures 5–10 in On the jumping spider Erica eugenia Peckham & Peckham 1892 (Araneae: Salticidae: Simonellini) from Brazil
Figures 5–10. Habitus of Erica eugenia from the Brazilian Cerrado. 5–7, Female: 5, Dorsal view. 6, Ventral view. 7, Lateral view. 8-10, Male: 8, Dorsal view. 9, Ventral view. 10, Lateral view.
Figure 5 in Construction of orb webs as nocturnal retreats by jumping spiders (Araneae: Salticidae: cf. Anarrhotus) in southwestern India
Figure 5. Salticids (cf. Anarrhotus) resting on their vertical platforms at night. 1-3, Spider resting on its platform at night. 2, Detailed view of this spider from (1). 3, Enhanced contrast image based on (1), showing layout of the hub and radii. 4, Detailed anterior view of salticid (cf. Anarrhotus) shown in Figure 4. Photographed in Kasaragod, Kerala by Prasantha Krishna.
Figures 2-7. 2-5 in New records of the exotic jumping spider Pseudeuophrys erratica (Araneae: Salticidae: Euophryini) in the United States
Figures 2-7. 2-5, Male Pseudeuophrys erratica in Essex County, Massachusetts. Photos by Richard Walton (CC-BY 3.0). 6, Male P. erratica in Pittsburgh, Pennsylvania. Photo by Ryan Kaldari (CC0 1.0). 7, Ventral view of left pedipalp of male P. erratica from Eugene, Oregon. Photograph by Ken Schneider (CC-BY 4.0).
Figures 17–20 in On the jumping spider Erica eugenia Peckham & Peckham 1892 (Araneae: Salticidae: Simonellini) from Brazil
Figures 17–20. Right pedipalp of Erica eugenia from the Brazilian Cerrado. 17, Ventral view. 18, Ventral-prolateral view. 19, Retrolateral view. 20, Prolateral view. B, bulbus; C, cymbium; Cu, cusp of cymbium; E, embolus; SD, spermatic ducts.
Figure 4 in Construction of orb webs as nocturnal retreats by jumping spiders (Araneae: Salticidae: cf. Anarrhotus) in southwestern India
Figure 4. Salticid (cf. Anarrhotus) resting on its vertical platform at night (1), and views of the empty platform on the next day (2-4), when the spider could not be found in the vicinity. 3-4, Enhanced contrast images based on (2), showing details of the densely woven platform at the hub and associated radii. A small packet that might represent the remains of insect can be seen near the spider, attached to the hub, but there was no sign that the web, not sticky or adhesive, played a role in prey capture. This spider jumped and moved to nearby branches when the web was disturbed. Photographed in Kasaragod, Kerala by Prasantha Krishna.
Fig. 10. Baryphas jullieni Simon, 1902 in Jumping spiders from Ivory Coast collected by J.-C. Ledoux (Araneae, Salticidae)
Fig. 10. Baryphas jullieni Simon, 1902, ♀ (MNHN). A–B. Epigyne. C–D. Internal structure of epigyne.
Fig. 1 in Jumping spiders from Ivory Coast collected by J.-C. Ledoux (Araneae, Salticidae)
Fig. 1. Location of J.-C. Ledoux's collecting sites of spiders in Ivory Coast.
Fig. 36 in Jumping spiders from Ivory Coast collected by J.-C. Ledoux (Araneae, Salticidae)
Fig. 36. Mexcala caerulea (Simon, 1901), ♀ (MNHN). A. Habitus, dorsal view. B. Epigyne.
Ultraconserved element data for phylogenomic placement of the jumping spider genus Iranattus Prószyński, 1992 (Salticidae, Plexippini, Plexippina)
<p>The jumping spider genus <em>Iranattus</em> Prószyński, 1992 has been placed in the Harmochirina based on morphology. We use phylogenomic evidence based on ultraconserved element (UCE) data to show that it belongs instead in the subtribe Plexippina.</p>
Seasonal footprints on ecological time series and jumps in dynamic states of protein configurations from a nonlinear forecasting method characterization (DataSet)
<p>Data from the article: <br>"Seasonal footprints on ecological time series and jumps in dynamic states of protein configurations from a nonlinear forecasting method characterization", L. Reyes, K. Campos, G. D. Avendaño, L. González-Paz, A. Vivas, Y. J. Alvarado, and S. Flores.</p> <p>Data to be used with some implementation of the forecasting method of reference:<br>Sugihara G. and May R. M., Nonlinear forecasting as a way of distinguishing chaos from measurement error in time series, <em>Nature</em> <strong>344</strong>, 734–741 (1990).</p>
Datasets relating to characterisation of Jumping Spider Rhodopsin-1 after reconstitution with retinal and retinal analogues
<p>001 - UV-Vis spectra JSR1 reconstituted with all-trans retinal, 9-cis retinal, ATR6.11 and 9CR6.11</p> <p>002 - UV-Vis spectra of JSR1 reconstituted with ATR6.11 and 9CR6.11, before and after acid denaturation</p> <p>003 - UV-Vis spectra of JSR1 reconstituted with ATR6.11, after addition of hydroxylamine</p> <p>004 - UV-Vis spectra of JSR1 reconstituted with 9CR6.11, after addition of hydroxylamine</p> <p>005 - UV-Vis spectra of illuminated JSR/ATR6.11 and JSR/9CR6.11</p> <p>006 - GTPase Glo Assay data measuring catalysis of nucleotide exchange in human G protein heterotrimers by JSR1/ATR6.11, JSR/9CR6.11 and JSR/9-cis retinal, with and without illumination</p> <p>007 - Size exclusion chromatograms JSR1/ATR6.11 after incubations with human Gi or human Gq heterotrimers</p> <p>008 - SDS-PAGE analysis of size exclusion chromatography peaks with JSR/ATR6.11 and human Gi or human Gq heterotrimers</p>
Modeling the early evolution of massive OB stars with an experimental wind routine. The first bi-stability jump and the angular momentum loss problem
<p>MESA run_star_extras associated with <a href="https://ui.adsabs.harvard.edu/?#abs/2017A&A...598A...4K">Keszthelyi et al. (2017)</a>. MESA version 7624.</p> <p>Publication DOI: <a href="https://doi.org/10.1051/0004-6361/201629468">10.1051/0004-6361/201629468</a></p>
Figure 7 in Rediscovery of Livilla radiata (Foerster, 1848) after 130 years in Hungary, with notes to the Fabaceae-associated jumping plant lice in Hungary (Insecta: Psylloidea)
Figure 7. Occurrences of Fabaceae-associated psyllids in Hungary.
Fig. 54. Pellenes purcelli Lessert, 1915 in Jumping spiders (Salticidae) of Uganda - revised list, new species and distributional data
Fig. 54. Pellenes purcelli Lessert, 1915, ♀ (MEU). A. General appearance. B–C. Epigyne.
Fig. 34 in Jumping spiders (Salticidae) of Uganda - revised list, new species and distributional data
Fig. 34. Hyllus leucomelas (Lucas, 1858), ♀ (FSCA). A. General appearance. B. Epigyne.
Fig. 1 in Jumping spiders (Salticidae) of Uganda - revised list, new species and distributional data
Fig. 1. Location of collecting sites of salticids in Uganda.
Figure 13. Grades 44 and 46. The philodromids also share a in A deeper phylogeny of jumping spiders (Araneae: Salticidae)
Figure 13. Grades 44 and 46. The philodromids also share a common ancestor with the salticids at grade 45.
Figure 11. Grades 31 and 37 in A deeper phylogeny of jumping spiders (Araneae: Salticidae)
Figure 11. Grades 31 and 37. The great majority of modern spiders are entelegynes, with separation of copulatory ducts from oviposition ducts (gonopores) of the female epigynum. Entelegynes in turn can be divided into two large groups, one (the RTA clade) distinguished by the presence of a retrolateral tibial apophysis on the male pedipalp.
Figure 10. Grades 27 and 28 in A deeper phylogeny of jumping spiders (Araneae: Salticidae)
Figure 10. Grades 27 and 28. There are many different mygalomorphs today, characterized by the parallel, parasagittal (orthognath) alignment of their chelicerae. The Theraphosidae is the largest family in the group, including the largest of all spiders. In some countries, these are popularly known as tarantulas, and kept as low-maintenance pets. Filistatids like this Filistata are near the base of araneomorph evolution. Their anterior medial spinnerets have fused to form a cribellum with many small ducts. This produces a kind of kinky silk that entangles prey in the webs of these spiders.
Figure 9. Grades 25 and 26. There are presently 126 in A deeper phylogeny of jumping spiders (Araneae: Salticidae)
Figure 9. Grades 25 and 26. There are presently 126 living species of whipscorpions (Uropygi) and they have a long fossil history dating back to the Pennsylvanian (Santana et al. 2024). The East Asian Mesothelae represent the most basal group of spiders, with two pairs of book lungs and four pairs of spinnerets at a central position on the underside of the opisthosoma. Note also the prominent tergites on the dorsal opisthosoma of this Liphistius, similar to those seen on Mastigoproctus.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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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.