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Figures 252–254 in Review of the genus Babycurus Karsch, 1886 (Arachnida, Scorpiones, Buthidae), with descriptions of Barbaracurus gen. n. and two new species from Oman and Yemen
Figures 252–254: Barbaracurus exquisitus comb. n. Right chelicera of male, dorsal (252), dorsointernal (253) and ventral (254) views. Paratype male, Jabal Shams, Oman, 14.X.1993. Scale bar: 500 µm.
Figures 208–218 in Review of the genus Babycurus Karsch, 1886 (Arachnida, Scorpiones, Buthidae), with descriptions of Barbaracurus gen. n. and two new species from Oman and Yemen
Figures 208–218: Barbaracurus yemenensis sp. n. Female holotype, chelicerae, carapace and tergites I–II (208), sternopectinal region and sternites III–IV (209), pedipalp chela, dorsal (210), external (211), and ventral (212) views, pedipalp patella, dorsal (213), external (214) and ventral (215) views, pedipalp femur and trochanter dorsal (216), internal (217), and ventral (218) views. The trichobothrial pattern is indicated in Figures 211–214 and 216–217 (white circles).
Figures 95–106 in Review of the genus Babycurus Karsch, 1886 (Arachnida, Scorpiones, Buthidae), with descriptions of Barbaracurus gen. n. and two new species from Oman and Yemen
Figures 95–106: Barbaracurus gen. n. Figures 95–98: Barbaracurus exquisitus comb. n. Figures 95, 97. Holotype male, chelicerae, carapace and tergites I–III (95) and sternopectinal region (97). Figures 96, 98. Paratype female, chelicerae, carapace and tergites I–III (96) and sternopectinal region (98). Figures 99–106: Distal segments of right legs, retrolateral views. Figures 99–100. B. exquisitus comb. n., male holotype, legs III (99) and IV (100). Figures 101–102. B. winklerorum sp. n., male holotype, legs III (101) and IV (102). Figures 103–106. B. yemenensis sp. n., female holotype, legs I–IV.
Figure 23-32 in Systematic revision of Gonaphodiellus taxa, with description of two new genera and fourteen new species (Coleoptera: Scarabaeidae: Aphodiinae)
Figure 23-32. Gonaphodiellus manantlanicus, new species (Las Joyas, Sierra de Manantlán, Jalisco, Mexico). 23) Epipharynx. 24-25) Habitus (length ideogram and morphological details). 26-27) Aedeagus (dorsal and lateral view). Gonaphodiellus martinpierai, new species (Acajete, Veracruz, Mexico). 28) Epipharynx. 29-30) Habitus (morphological details and length ideogram). 31-32) Aedeagus (dorsal and lateral view).
Fig. 11 in Description of two new species of Oecetis (Trichoptera, Leptoceridae) from Borneo
Fig. 11. Map with the position of the two sampling sites in Maliau Basin shown as orange dots. The position of the Maliau Basin area on Borneo is indicated with a blue rectangular in the upper-left map.
Figs 6–10 in Description of two new species of Oecetis (Trichoptera, Leptoceridae) from Borneo
Figs 6–10. Oecetis apelqvisti sp. nov., holotype, ♂ (NHRS). 6. Genitalia, lateral view. 7. Genitalia, dorsal view. 8. Genitalia, ventral view. 9. Phallus, lateral view. 10. Phallus, ventral view. Scale bar = 0.1 mm.
Figs 1–5 in Description of two new species of Oecetis (Trichoptera, Leptoceridae) from Borneo
Figs 1–5. Oecetis mesospina sp. nov., holotype, ♂ (NHRS). 1. Genitalia, lateral view. 2. Genitalia, dorsal view. 3. Genitalia, ventral view. 4. Phallus, lateral view. 5. Phallus, ventral. Scale bar = 0.1 mm.
FIG. 2 in Five new records and two new reports of Cotoneaster Medik. (Rosaceae) for the Flora of Iran
FIG. 2. — Cotoneaster transcaucasicus Pojark.: A, habit; B, leaves and fruits. Collection number: Maroofi & Naseri 6520 (HKS); determined by Raei Niaki & Attar.
FIG. 7 in Five new records and two new reports of Cotoneaster Medik. (Rosaceae) for the Flora of Iran
FIG. 7. — Cotoneaster meyeri Pojark. leaves and fruits outline (A) and close up (B). Collection number: Raei Niaki & Mahdigholi 46883 (TUH); determined by Raei Niaki & Attar.
FIG. 8 in Five new records and two new reports of Cotoneaster Medik. (Rosaceae) for the Flora of Iran
FIG. 8. — Cotoneaster insignis Pojark. leaves and fruits outline (A) and close up (B). Collection number: Attar, Raei Niaki & Zamani 37454 (TUH); determined by Raei Niaki & Attar.
FIG. 6 in Five new records and two new reports of Cotoneaster Medik. (Rosaceae) for the Flora of Iran
FIG. 6. — Cotoneaster ellipticus (Lindl.) Hort ex Loudon outline (A) and close up of leaves (B) and fruit (C). Collection number: Memariani, Zangooei & Arjmandi 43358 (FUMH); determined by Raei Niaki & Attar.
FIG. 3. — Cotoneaster minutus G in Five new records and two new reports of Cotoneaster Medik. (Rosaceae) for the Flora of Iran
FIG. 3. — Cotoneaster minutus G.Klotz leaves and fruits outline (A) and close up (B). Collection number: Memariani & Arjmandi 44626 (FUMH); determined by Raei Niaki & Attar.
FIG. 5. — Cotoneaster aitchisonii C.K in Five new records and two new reports of Cotoneaster Medik. (Rosaceae) for the Flora of Iran
FIG. 5. — Cotoneaster aitchisonii C.K.Schneid. outline (A) and close up of leaves (B) and fruit (C). Collection number: Memariani, Zangooei & Arjmandi 43351 (FUMH); determined by Raei Niaki & Attar.
FIG. 1 in Five new records and two new reports of Cotoneaster Medik. (Rosaceae) for the Flora of Iran
FIG. 1. — Map showing location of new records and reports of Cotoneaster species in Irano-Turanian (green symbols) and ecotones between Irano-Turanian and Eurosiberian regions (blue symbols).
FIG. 4. — Cotoneaster afghanicus G in Five new records and two new reports of Cotoneaster Medik. (Rosaceae) for the Flora of Iran
FIG. 4. — Cotoneaster afghanicus G.Klotz leaves and fruits outline (A) and close up (B). Collection number: Faghihnia & Zangooei 27111 (FUMH); determined by Raei Niaki & Attar.
How flexible, slit and rigid barriers mitigate two-phase geophysical mass flows: a numerical appraisal
<p>The supplementary videos SV1 and SV2 (presented in Figures 4 and 5) show geophysical flows impacting flexible, slit, and rigid barriers via pile-up mode and runup mode, respectively.</p> <p>The measurement data used for comparison in Figure 7 from 14 centrifuge tests with bouldery and the boulder-debris mixture flows (Song et al., 2018b, 2019), and dry granular flow against open-type dams (Choi et al., 2020) were published open access in their articles.</p> <p>The unique dataset, comprising normalized data obtained from analytical models (Li et al., 2021; Song et al., 2021a), empirical relations (Cui et al., 2015), experiments (Armanini et al., 2020; Choi et al., 2020; Cui et al., 2015; Hu et al., 2020; Song et al., 2021a, 2021b; Tiberghien et al., 2007; Vicari et al., 2021), field events (Hübl et al., 2009), and practical design values (Armanini, 1997; Hungr et al., 1984; Kwan & Cheung, 2012; Wendeler, 2016), is plotted in Figure 10 for comparison.</p> <p>All these articles can be found in the PDF file entitled “References in Figures 7 and 10”.</p>
Hippocampal CA1 pyramidal cell membrane voltage recorded in response to noise stimuli at two temperatures.
<p>Electrophysiological recording of the membrane voltage (whole-cell patch-clamp) of three hippocampal CA1 pyramidal cells. Cells are stimulated with a current step chosen to ensure a firing rate around 5-10Hz (amplitude of the current step is given in the filenames) and a noise stimulus with zero mean (Ornstein-Uhlenbeck process with 4ms timescale). Each CSV file contains three columns, the timepoints (saved at 10000Hz), the noise stimulus, and the voltage trace recorded in response to the given noise stimulus. Voltages are recorded at low temperatures (around 32 degrees Celsius) and at high temperatures (around 37 degrees Celsius for cell 1, around 40 degrees Celsius for cells 2 and 3), exact temperatures are given in the filenames. The file metadata.csv contains additional information.</p>
Data from: Adaptive division of growth and development between hosts in helminths with two-host life cycles
<p>Parasitic worms (helminths) with complex life cycles divide growth and development between successive hosts. Using data from 597 species of acanthocephalans, cestodes, and nematodes with two-host life cycles, we found that helminths with larger intermediate hosts were more likely to infect larger, endothermic definitive hosts, although some evolutionarily shifts in definitive host mass occurred without changes in intermediate host mass. Life-history theory predicts parasites to shift growth to hosts in which they can grow rapidly and/or safely. Accordingly, helminth species grew relatively less as larvae and more as adults if they infected smaller intermediate hosts and/or larger, endothermic definitive hosts. Growing larger than expected in one host, relative to host mass/endothermy, was not associated with growing less in the other host, implying a lack of cross-host tradeoffs. Rather, some helminth orders had both large larvae and large adults. Within these taxa, though, size at maturity in the definitive host was unaffected by changes to larval growth, as predicted by optimality models. Parasite life-history strategies were mostly (though not entirely) consistent with theoretical expectations, suggesting that helminths adaptively divide growth and development between the multiple hosts in their complex life cycles.</p>
Fig. 3 in Two new species of Indonemoura (Plecoptera, Nemouridae) from Yunnan Province, China
Fig. 3. Habitat of Indonemoura yingjiangensis Bai & Qian sp. nov. and In. longihamata Bai & Qian sp. nov. in Tongbiguan Provincial Nature Reserve. A. The upper reaches of unknown streams. B. The lower reaches of unknown streams.
Fig. 2 in Two new species of Indonemoura (Plecoptera, Nemouridae) from Yunnan Province, China
Fig. 2. Indonemoura longihamata Bai & Qian sp. nov., holotype, ♂ (SWFU). A. Habitus, dorsal view. B. Head and prothorax, ventral view. C. Terminalia, dorsal view. D. Terminalia, ventral view. E. Terminalia, lateral view.
ScienceDex guides
Understand access before you commit
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.