Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
485
datasets available to search
ShareScore release 0.9.0
Dataset results
485 results for “cooking”
Reanalysis accounting for clustering and nesting overturns conclusions in: "Watching TV Cooking Programs: Effects on Actual Food Intake Among Children"
<p>Stata code to reproduce results from Folkvord F, Anschütz D, Geurts M. Watching TV cooking programs: effects on actual food intake among children. <em>J Nutr Educ Behav</em>. 2020;52(1):3-9.</p>
Relationship of thermal treatment and antioxidant capacity in cooked foods
<p>This is supplemental information of the paper "Relationship of thermal treatment and antioxidant capacity in cooked foods", submitted for publication to Antioxidants.</p>
Figure 21 in Drosophilidae (Diptera) of the Cook Islands
Figure 21. Distribution map of 12 species of the Drosophila ananassae complex. This map was first published by McEvey & Schiffer (2015) and then updated by them (2018). The discovery of the new species D. rarotongae sp. nov. from the southern group of Cook Islands is indicated on this map. Drosophila ananassae s.str. has pantropical distribution indicated within the pale blue lines, the Ambon type locality is shown. Three or more additional but undescribed species occur in New Guinea (and perhaps also in northern Australia), these are not shown (see McEvey & Schiffer, 2015, for further details).
Figures 22–30 in Drosophilidae (Diptera) of the Cook Islands
Figures 22–30. Hypandria of Drosophila rarotongae sp. nov. and related species: (22) D. atripex, Bali, McE32697; (23) D. monieri, Moorea, AM K.380298; (24) D. ochrogaster, New Caledonia, K.282803; (25) D. schugi, Samoa, K.356978; (26) D. rarotongae, Rarotonga, K.385584; (27) D. phaeopleura, Fiji, K.282923; (28) D. pandora, Lake Placid (near Cairns), ex iso-female strain CAQ425; (29) D. ananassae, Marquesas, K.380299; (30) D. anomalata, Townsville, ex type strain CHC221. Abbreviations, see Figs 13–20 caption.
Figure 2 in Drosophilidae (Diptera) of the Cook Islands
Figure 2. Montane forest terrain of Rarotonga showing the relationship between the three "high elevation" collecting sites in the upper Avatiu valley (circles, details in Table 2), close to the more inaccessible higher mountain peaks which could not be reached during the present survey—Te Manga, Te Atkura, Te Kou, and Maungatea. (Colour photo by Marcus Gleinig, terrain image [Te Kou to Te Manga profile distortion due to steepness of gradient] from Google Earth, June 2019).
Figures 13–20 in Drosophilidae (Diptera) of the Cook Islands
Figures 13–20. Drosophila rarotongae sp. nov. (13) male habitus; (14) arista of AM K.385602; (15) wing of AM K.385592; (16, 17) ventrolateral and dorsal views respectively, of hypandrium of AM K.385594 and K.385584—aed, aedeagus; gon s, gonopodal seta (one of a pair); goncx, gonocoxite; pgt, postgonite; phapod, phallapodeme; pregt, pregonite; pregt proc pregonite process; pregt sens, pregonite sensilla (three sensilla detected on this structure under high power); prens, prensisetae (lower of two series, upper series with two prensisetae); trn bd, transverse band; (18) epandrium of AM K.385594; (19) oviscapt of female AM K.385600; and (20) sex combs on foretarsi of male AM K.385592.
Figures 3–10 in Drosophilidae (Diptera) of the Cook Islands
Figures 3–10. Comparison of Drosophila sp. aff. funebris from Cook Islands (left) and D. funebris (right): (3, 4) lateral views of head; (5, 6) dorsal views of cephalo-chaetotaxy, back of head, and scutum anteriorly; (7, 8) ratio of heavy to light costal setation in third costal section of wing—almost entire in Cook Island specimen, only about 0.4 in D. funebris (see Table 4); and (9–10) costal spine size at subcostal break (second spine of pair broken off in Fig. 9 photo). All specimens in AM: Figs 3, 5, 7, 9—K.471932 (Rarotonga); Figs 4 (K.353509), 6 (K.353514), 8 (K.353510), and 10 (K.353614) (all D. funebris from Johannesburg). Scale is 200 µm.
Figures 34–41 in Drosophilidae (Diptera) of the Cook Islands
Figures 34–41. Scaptodrosophila bryani (Malloch), lateral views of males (34–37, K.393581–82, K.393583) and females (38–40, K.393585–87); anterior, middle, and posterior katepisternal setae (kepst s) indicated (36–37); detail of setae arising from scutellum (ap sctl s, apical scutellar seta, long; b sctl s, basal scutellar seta, short) and posterior part of scutum (41). All with label data: "COOK IS, Mangaia | –21.9531° –157.9148° | 7.ii.2017 ... fruit | Michal Polak" except Figs. 37 and 41: "NT Casuarina urban | 12.3731°S 130.8864°E | fruit compost 28.ix.2009 | S. McEvey & M. Braby". All in AM.
Figures 31–33 in Drosophilidae (Diptera) of the Cook Islands
Figures 31–33. Drosophila bipectinata Duda males, with detail of sex combs of male foreleg. Specimens in AM registered K.385867, K.385864 and K.385869.001 with label data: "COOK IS, Aitutaki | –18.8549° –159.7884° | 10.ii.2017 fruit | Michal Polak".
Fig. 7 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 7. Left gonopod of Oxidus riukiaria (Verhoeff, 1940), from sample IEBR-H470. A. Lateroventral view. B. Ventral view. C. Postfemoral region, ventral view. Note: z = spine z, but broken.
Fig. 10 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 10. Phylogenetic tree of the genus Oxidus and some closely related groups based on Maximum Likelihood and Bayesian Inference Analysis of a 991 bp fragment of the combination of 16S rRNA and COI genes.
Fig. 9 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 9. Phylogenetic tree of the genus Oxidus and some closely related groups based on Maximum Likelihood and Bayesian Inference Analysis of a 525 bp fragment of the COI gene (# = a value less than 65%).
Fig. 3 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 3. Oxidus gigas (Attems, 1953) from Duc Xuan Commune, Ha Giang Prov., Vietnam. A. Entire body, length ca 34 mm. B–C. Segments 8–9–10. B. ♂. C. ♀. Scale bars = 1 mm. (photo by Anh Nguyen)
Fig. 1 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 1. Oxidus gracilis (C.L. Koch, 1847) from Okinawa Island, Japan. A. Entire body, length ca 23 mm. B–C. Segments 8–9–10. B. ♂. C. ♀. Scale bars = 1 mm. (photos by Z. Korsós)
Fig. 2 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 2. Left gonopod of Oxidus gracilis (C.L. Koch, 1847), sample IEBR-USA. A. Lateral view. B. Mesal view. Scale bars = 100 µm.
Fig. 6 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 6. Left gonopod of Oxidus riukiaria (Verhoeff, 1940). A. Lateral view. B. Postfemoral region, lateral view. Redrawn from Verhoeff 1940. No scale bars.
Fig. 4 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 4. Right gonopod of Oxidus gigas (Attems, 1953), from sample IEBR-Myr 113. A. Lateral view. B. Ventral view. C. Mesal view. The picture has been Fipped horizontally. Scale bars = 1 um.
Fig. 5 in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 5. Oxidus riukiaria (Verhoeff, 1940) from Okinawa, Japan. A. Entire body, length ca 20 mm. B–C. Segments 8–9–10. B. ♂. C. ♀. Scale bars = 1 mm. (photos by Z. Korsós)
Fig. 8. A in A revision and phylogenetic analysis of the millipede genus Oxidus Cook, 1911 (Polydesmida, Paradoxosomatidae)
Fig. 8. A. Left gonopod of Oxidus avia (Verhoeff, 1937), lateral view. B. Right gonopod of Oxidus obtusus (Takakuwa, 1942), mesal view. Redrawn from Verhoeff 1937 and Takakuwa 1942a, respectively. No scale bars.
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)].
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.