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Text-fig. 7. Enamel ultrastructure of P3, Equus caballus (konik polski). a: enamel row, scale bar = 50 Μm; b: type I and III, scale bar = 50 Μm; c: type I, scale bar = 10 Μm; d, e: wavy enamel of TZ with decussations, scale bar = 100 and 50 Μm respectively; f: type II near OES, scale bar = 10 Μm. in The Ultrastructure Of The Tooth Enamel Of Small Equus Of The "Tarpan" Group And Their Possible Phylogenetic Connections
Text-fig. 7. Enamel ultrastructure of P3, Equus caballus (konik polski). a: enamel row, scale bar = 50 Μm; b: type I and III, scale bar = 50 Μm; c: type I, scale bar = 10 Μm; d, e: wavy enamel of TZ with decussations, scale bar = 100 and 50 Μm respectively; f: type II near OES, scale bar = 10 Μm.
Text-fig. 6. Correlation of the Cheringoma and Mazamba formations on the basis of benthic foraminiferans and mammals respectively. Identifications of foraminiferans are from Newton (1924) and Abrard (1928), and the ranges of foraminiferans are from Sella-Kiel et al. (1998). The time scale is from Gradstein et al. (2020). The distribution of Nummulites atacicus is included, but it is not known whether it is reworked from older deposits. If the identification is valid, it would support the thesis that there was a period of Ypresian deposition in the vicinity during which remains of the species were fossilised. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 6. Correlation of the Cheringoma and Mazamba formations on the basis of benthic foraminiferans and mammals respectively. Identifications of foraminiferans are from Newton (1924) and Abrard (1928), and the ranges of foraminiferans are from Sella-Kiel et al. (1998). The time scale is from Gradstein et al. (2020). The distribution of Nummulites atacicus is included, but it is not known whether it is reworked from older deposits. If the identification is valid, it would support the thesis that there was a period of Ypresian deposition in the vicinity during which remains of the species were fossilised.
Text-fig. 2. Stratigraphic column of the Govone section with a detail of the sampled intervals on the right. CCS – Cassano Spinola Conglomerates; Gm and Gg – sedimentary cycles, respectively marl-dominated or gypsum-dominated; MES – Messinian Erosional Surface; MSC – Messinian Salinity Crisis; PLG – Primary Lower Gypsum; RLG – Resedimented Lower Gypsum. in Remains Of A Subtropical Humid Forest In A Messinian Evaporitebearing Succession At Govone, Northwestern Italy - Preliminary Results
Text-fig. 2. Stratigraphic column of the Govone section with a detail of the sampled intervals on the right. CCS – Cassano Spinola Conglomerates; Gm and Gg – sedimentary cycles, respectively marl-dominated or gypsum-dominated; MES – Messinian Erosional Surface; MSC – Messinian Salinity Crisis; PLG – Primary Lower Gypsum; RLG – Resedimented Lower Gypsum.
Text-fig. 3. a: Pterigophycos sp., whole-plant specimen, coll. No. 22.116, larger blades denoted B1–4 (for details, see text), scale bar = 2 cm; b: Close-up of blades B1 and B2, which resemble P. spectabilis A.MASSAL. and P. canossae A.MASSAL., respectively; c: Closeup of blade B3 resembling P. canossae; d: Close-up of blade B4 resembling P. gazolanus A.MASSAL. or Laminarites irideaephyllus A.MASSAL. Scale bars = 1 cm unless otherwise stated. in A Whole-Plant Specimen Of The Marine Macroalga Pterigophycos From The Eocene Of Bolca (Veneto, N-Italy)
Text-fig. 3. a: Pterigophycos sp., whole-plant specimen, coll. No. 22.116, larger blades denoted B1–4 (for details, see text), scale bar = 2 cm; b: Close-up of blades B1 and B2, which resemble P. spectabilis A.MASSAL. and P. canossae A.MASSAL., respectively; c: Closeup of blade B3 resembling P. canossae; d: Close-up of blade B4 resembling P. gazolanus A.MASSAL. or Laminarites irideaephyllus A.MASSAL. Scale bars = 1 cm unless otherwise stated.
Figure 4: Complexity of geographical space with respect of emergent organizations-MODELING SELF-ORGANIZING SYSTEMS WITH SOCIAL INSECTS ALGORITHMS
<p>The applications we focus on in the models that we will propose in the<br> following, concerns specifically the multi-center (or multi-organizational) phenomona<br> inside urban development. As an artificial ecosystem, the city development<br> has to deal with many challenges, specifically for sustainable development,<br> mixing economical, social and environmental aspects. The decentralized<br> methodology proposed in the following allows to deal with multi-criteria problems,<br> leading to propose a decision making assistance, based on simulation<br> analysis.</p>
→ Fig. 9. Antiarchan fish Bothriolepis leptocheira jeremejevi (Rohon, 1900), Sosnogorsk locality, Sosnogorsk Formation, lowermost Famennian, anterior median dorsal (A–G) and posterior median dorsal (H–M) plates of the trunk armour. A. IG KSC 155/5 in dorsal (A1) and visceral (A2) views. B. IG KSC 155/108 in dorsal (B1) and visceral (B2) views. C. IG KSC 155/97 in dorsal view. D. IG KSC 155/113 in dorsal (D1) and visceral (D2) views. E. IG KSC 155/140 in dorsal (E1) and visceral (E2) views. F. Impression of the dorsal surface of IG KSC 155/42. G. IG KSC 155/44 in dorsal view. H. Fragment of IG KSC 155/7 in dorsal view. I. IG KSC 155/1 in dorsal (I1) and visceral (I2) views. J. IG KSC 155/71 in dorsal view. K. Slightly deformed IG KSC 155/70 in dorsal (K1) and visceral (K2) views. L. IG KSC 155/158 in dorsal view. M. IG KSC 155/157 in dorsal (M1) and visceral (M2) views. Abbreviations: ADL, anterior dorso-lateral plate; alr, postlevator thickening; AMD, anterior median dorsal plate; cf.ADL, cf.AMD, and cf.MxL, area overlapping ADL, AMD or MxL respectively; cr.tp, posterior transversal internal crest; dlg1 and dlg2, anterior and posterior oblique dorsal sensory line groove; dma, tergal angle; dmr, dorsal median ridge; f.retr, levator fossa; grm, ventral median groove; l, lateral corner; mvr, median ventral ridge; MxL, mixilateral plate; npn, postnuchal notch; oa.ADL, oa.MxL and oa.PMD, area overlapped by ADL, MxL or PMD respectively; pa, posterior corner; pma, posterior marginal area; PMD, posterior median dorsal plate; pr.p, posterior process of AMD; pr.pl, external postlevator process; prv2, posterior ventral process of dorsal wall of trunk armour; pt1 and pt2, anterior and posterior ventral pit; pua, posterior unornamented area of PMD; rf, "round fossula"; sna, supranuchal area; tb, ventral tuberosity. in A new assessment of the Late Devonian antiarchan fish Bothriolepis leptocheira from South Timan (Russia) and the biotic crisis near the Frasnian-Famennian boundary
→ Fig. 9. Antiarchan fish Bothriolepis leptocheira jeremejevi (Rohon, 1900), Sosnogorsk locality, Sosnogorsk Formation, lowermost Famennian, anterior median dorsal (A–G) and posterior median dorsal (H–M) plates of the trunk armour. A. IG KSC 155/5 in dorsal (A1) and visceral (A2) views. B. IG KSC 155/108 in dorsal (B1) and visceral (B2) views. C. IG KSC 155/97 in dorsal view. D. IG KSC 155/113 in dorsal (D1) and visceral (D2) views. E. IG KSC 155/140 in dorsal (E1) and visceral (E2) views. F. Impression of the dorsal surface of IG KSC 155/42. G. IG KSC 155/44 in dorsal view. H. Fragment of IG KSC 155/7 in dorsal view. I. IG KSC 155/1 in dorsal (I1) and visceral (I2) views. J. IG KSC 155/71 in dorsal view. K. Slightly deformed IG KSC 155/70 in dorsal (K1) and visceral (K2) views. L. IG KSC 155/158 in dorsal view. M. IG KSC 155/157 in dorsal (M1) and visceral (M2) views. Abbreviations: ADL, anterior dorso-lateral plate; alr, postlevator thickening; AMD, anterior median dorsal plate; cf.ADL, cf.AMD, and cf.MxL, area overlapping ADL, AMD or MxL respectively; cr.tp, posterior transversal internal crest; dlg1 and dlg2, anterior and posterior oblique dorsal sensory line groove; dma, tergal angle; dmr, dorsal median ridge; f.retr, levator fossa; grm, ventral median groove; l, lateral corner; mvr, median ventral ridge; MxL, mixilateral plate; npn, postnuchal notch; oa.ADL, oa.MxL and oa.PMD, area overlapped by ADL, MxL or PMD respectively; pa, posterior corner; pma, posterior marginal area; PMD, posterior median dorsal plate; pr.p, posterior process of AMD; pr.pl, external postlevator process; prv2, posterior ventral process of dorsal wall of trunk armour; pt1 and pt2, anterior and posterior ventral pit; pua, posterior unornamented area of PMD; rf, "round fossula"; sna, supranuchal area; tb, ventral tuberosity.
А – типовые местонахоЖдениЯ: Зал. ЛаврентиЯ (красный маркер), б. ПровидениЯ (Зеленый маркер); B, B' – иЗобраЖениЯ раковины (B) и Зуба радулы (B') Bela violacea var. nodulosa. Вр=14.5 мм, ДЗ=0.25 мм, иЗ: Krause [1885, pl. 18, figs. 4, 12]; C, C' – синтип Bela violacea var. nodulosa (C) и увеличенный участок предпоследнего оборота (C'), ZMB 37860, Вр=12 мм (фотографиЯ – с раЗрешениЯ ZMB); D–I – иЗменчивость Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN беЗ номера, ЗФИ, о-в Аполлонова, Американский Залив, 3–4 м. Вр=8.2 мм; E – Defrancia becki. ZIN беЗ номера, ЗФИ, о-в Кука, 3–4 м. Вр=9.1 мм; F – Bela violacea var. laevior. Вр=12 мм, иЗ: Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Баренцево море, Югорский Шар, 13 м. Вр=8.7 мм; H – Pleurotoma bicarinata. ZIN 41203/156, ЗФИ, о-в ГрЭм-БЭм, 12–15 м. Вр=8.4 мм; I, I' – Зубы радулы типичной (I) и беЗкилевой (I') форм. ДЗ=0.12 мм и 0.21 мм, соответственно, иЗ: [Sars, 1878, pl. 9, figs. 7, 8]; J – иЗобраЖение раковины Lora inequita. Вр=11 мм, иЗ: Dall [1919, pl. 16, fig. 9]; K – голотип Lora inequita, USNM 222238. Вр=11 мм (фотографиЯ – с раЗрешениЯ USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: раковины (L) и Зуб радулы (L'). Вр=12 мм и 11.6 мм, соответственно, ДЗ=0.15 мм, иЗ: Богданов [1990, рис. 175, 176, 422 (7)]. A – type localities: Lawrence Bay (red circle), Providence Bay (green circle); B, B' – images of the shell (B) and tooth of the radula (B') of Bela violacea var. nodulosa. H=14.5 mm, L=0.25 mm, after Krause [1885, pl. 18, figs. 4, 12]; C, C' – a syntype of Bela violacea var. nodulosa (C) and the enlarged section of the penultimate whorl (C'), ZMB 37860, H=12 mm (photo – courtesy of ZMB); D–I – variability of Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN uncatalogued, Franz Josef Land, Apollonova Isl., American Gulf, 3–4 m. H=8.2 mm; E – Defrancia becki. ZIN uncatalogued, Franz Josef Land, Cook Isl., 3–4 m. H=9.1 mm; F – Bela violacea var. laevior. H=12 mm, after Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Barents Sea, Ugra Shar, 13 m. H=8.7 mm; H – Pleurotoma bicarinata. ZIN 41203/156, Franz Josef Land, Graham-Bam Isl., 12–15 m. H= 8.4 mm; I, I' – teeth of typical (I) and keelless (I') forms. L=0.12 mm and 0.21 mm, respectively; after Sars [1878, pl. 9, figs. 7,8]; J – image of Lora inequita. H=11 mm, after Dall [1919, pl.16, fig. 9]; K – the holotype of Lora inequita, USNM 222238. H=11 mm (photo – courtesy of USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: shells (L) and tooth (L'). H=12 mm and 11.6 mm, respectively, L=0.15 mm, after Bogdanov [1990, figs. 175, 176, 422 (7)]. in Curtitoma nodulosa (Krause, 1885) comb. nov. (Gastropoda: Mangeliidae), a rare species twice described from the northern part of Bering Sea
А – типовые местонахоЖдениЯ: Зал. ЛаврентиЯ (красный маркер), б. ПровидениЯ (Зеленый маркер); B, B' – иЗобраЖениЯ раковины (B) и Зуба радулы (B') Bela violacea var. nodulosa. Вр=14.5 мм, ДЗ=0.25 мм, иЗ: Krause [1885, pl. 18, figs. 4, 12]; C, C' – синтип Bela violacea var. nodulosa (C) и увеличенный участок предпоследнего оборота (C'), ZMB 37860, Вр=12 мм (фотографиЯ – с раЗрешениЯ ZMB); D–I – иЗменчивость Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN беЗ номера, ЗФИ, о-в Аполлонова, Американский Залив, 3–4 м. Вр=8.2 мм; E – Defrancia becki. ZIN беЗ номера, ЗФИ, о-в Кука, 3–4 м. Вр=9.1 мм; F – Bela violacea var. laevior. Вр=12 мм, иЗ: Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Баренцево море, Югорский Шар, 13 м. Вр=8.7 мм; H – Pleurotoma bicarinata. ZIN 41203/156, ЗФИ, о-в ГрЭм-БЭм, 12–15 м. Вр=8.4 мм; I, I' – Зубы радулы типичной (I) и беЗкилевой (I') форм. ДЗ=0.12 мм и 0.21 мм, соответственно, иЗ: [Sars, 1878, pl. 9, figs. 7, 8]; J – иЗобраЖение раковины Lora inequita. Вр=11 мм, иЗ: Dall [1919, pl. 16, fig. 9]; K – голотип Lora inequita, USNM 222238. Вр=11 мм (фотографиЯ – с раЗрешениЯ USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: раковины (L) и Зуб радулы (L'). Вр=12 мм и 11.6 мм, соответственно, ДЗ=0.15 мм, иЗ: Богданов [1990, рис. 175, 176, 422 (7)]. A – type localities: Lawrence Bay (red circle), Providence Bay (green circle); B, B' – images of the shell (B) and tooth of the radula (B') of Bela violacea var. nodulosa. H=14.5 mm, L=0.25 mm, after Krause [1885, pl. 18, figs. 4, 12]; C, C' – a syntype of Bela violacea var. nodulosa (C) and the enlarged section of the penultimate whorl (C'), ZMB 37860, H=12 mm (photo – courtesy of ZMB); D–I – variability of Curtitoma violacea: D – Pleurotoma violacea var. brevis. ZIN uncatalogued, Franz Josef Land, Apollonova Isl., American Gulf, 3–4 m. H=8.2 mm; E – Defrancia becki. ZIN uncatalogued, Franz Josef Land, Cook Isl., 3–4 m. H=9.1 mm; F – Bela violacea var. laevior. H=12 mm, after Sars [1878, pl. 17, fig. 3]; G – Bela bicarinata var. geminolineata. ZIN 21324/28, Barents Sea, Ugra Shar, 13 m. H=8.7 mm; H – Pleurotoma bicarinata. ZIN 41203/156, Franz Josef Land, Graham-Bam Isl., 12–15 m. H= 8.4 mm; I, I' – teeth of typical (I) and keelless (I') forms. L=0.12 mm and 0.21 mm, respectively; after Sars [1878, pl. 9, figs. 7,8]; J – image of Lora inequita. H=11 mm, after Dall [1919, pl.16, fig. 9]; K – the holotype of Lora inequita, USNM 222238. H=11 mm (photo – courtesy of USNM); L, L' – Oenopota inequita sensu Bogdanov non Dall: shells (L) and tooth (L'). H=12 mm and 11.6 mm, respectively, L=0.15 mm, after Bogdanov [1990, figs. 175, 176, 422 (7)].
Figures represent five groups respectively. In group, when the dispersal rate is equal to 1% values of the probability of disperser survival are 1, 0.9, 0.8, 0.7, 0.6, 0.5 respectively as in groups and in The Influence Of Dispersal On The Metapopulation Viability Of Giant Panda (Aliuropoda Melanoleuca) In The Minshan Mountains
Figures represent five groups respectively. In group, when the dispersal rate is equal to 1% values of the probability of disperser survival are 1, 0.9, 0.8, 0.7, 0.6, 0.5 respectively as in groups and
Fig. 14 in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 14. Grasping pattern of the hand. A. Grasping a bough of the tree; B. Holding a piece of fruit. Sketches are drawn imitating the hand motion shown in movies of NHK BS TV program (Yamagiwa, 2012).
Fig. 13. Knuckle walk. A in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 13. Knuckle walk. A. The trunk tilts backward because of longer forelimbs; B. The knuckle walk of gorillas is walking with MP joints in extension and PIP joints in deep flexion bearing the weight on the dorsal aspects of the middle phalanges of the hands. Sketches are drawn imitating the walking style shown in movies of NHK BS TV program (Yamagiwa, 2012).
Fig. 12 in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 12. Dorsal aspect of the metacarpophalangeal joint. A. A shallow groove (white arrows) is seen along the dorsal margin of the articular cartilage of the metacarpal head; B. The dorsal edge of the proximal phalanx base sits in the groove by extending the MP joint passively; C. Grooves are deep enough at the 3rd and 4th metacarpals (white arrows), but not at the 2nd and 5th in the skeletal specimen of another gorilla stored in National Museum of Nature and Science.
Fig. 11. Extensor apparatus and retaining ligaments. A in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 11. Extensor apparatus and retaining ligaments. A. Extensor apparatus consists of two components: extrinsic compornent (dark green) and intrinsic component (light green). Ligamentous structures are shown in orange color. The interosseous hood is the proximal hood-like portion of the aponeurotic expansion of the interosseous tendon (a thick arrow). (modified from Tubiana and Valentin, 1964); B. On the radial side of the middle finger, the interosseous hood is shown. Adherent to the proximal margin of this interosseous hood, a sagittal band expands between DTML and EDC tendon; C. The oblique retinacular ligament (ORL) is well developed at the radial aspect.
Fig. 9. Underdeveloped EIP. A in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 9. Underdeveloped EIP. A small slender muscle sitting at the dorsoradial aspect of the ulna is judged to be underdeveloped EIP muscle although its tendon attaches to the dorsal aspect of the wrist (a white block arrow).
Fig. 7 in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 7. Innervation of intrinsic muscles by the radial bundle of UABM. The radial bundle first gives off branches to the hypothenar muscles and to the lumbrical muscles of the little and ring fingers (marked with asterisks), and then to interossei (4th DI, 3rd PI and 3rd DI, 2nd PI).
Fig. 15 in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 15. The mechanism to block hyperextension of the MP joint with the function of the sagittal band. A. When the finger is flexed, the sagittal band passes over the joint axis of the metacarpal head in coordination with the distalward movement of the extensor tendon; B. When the MP joint is extended and surpasses the range of extension, the traction force of the finger extensor is blocked with the tightened sagittal band that transmits the force palmarward so that the proximal phalanx base does not move further to hyperextension.
Fig. 5 in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 5. Palmar aspect of the proximal phalanx. An osseous crest is seen along each edge of the palmar aspect of the phalanx and the groove is formed between those crests. The head of the proximal phalanx slants palmarward.
Fig. 3. Underdeveloped thumb flexor. A in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 3. Underdeveloped thumb flexor. A. The tendon of the thumb flexor is much thinner than that of FDS or FDP; B. Its muscle belly (uFPL) bifurcates from the distal portion of FDP muscle of the index finger; C. Pulling FDP index finger at its myotendinous junction with a retractor revealed that the thumb and the index finger were flexed simultaneously.
Fig. 4. Finger flexor sheath and pulley system. A in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 4. Finger flexor sheath and pulley system. A. The entire sheath of the finger flexor of the ring finger is shown with the names of individual pulleys. The very thick and wide A2′ pulley (a white thick arrow) is located between A2 and C1; B. The inner surface of the sheath showing that A2′ pulley is twice as wide as A3.
Fig. 2 in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 2. The subcutaneous structures of the palm. A. The palmar aponeurosis is absent except for its most distal parts: natatory ligaments (white arrows); B. The ligamentous fibers (white arrows) arising from the distal margin of the flexor retinaculum; C. Ligamentous septum (a white arrow) along the flexor tendon formed with those ligamentous fibers.
Fig. 10 in Anatomical Study of the Right Forearm and Hand of One Western Gorilla (Gorilla gorilla) for Comparison with Humans with Respect to Motions of the Thumb and Fingers
Fig. 10. The insertions of the first dorsal interosseous muscle. A. The distal portion of the 1st DI muscle is voluminously muscular and passes into the tendinous portion of the interosseous hood at the level of the proximal portion of the proximal phalanx; B. The tendinous insertion to the proximal phalanx base is exposed by reflect- ing the extensor apparatus. The tendon has been divided to explore the deeper structure and then re-sutured.
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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.