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41,236 results for “Review of reviews”
Figs. 179–188 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 179–188. Alienocacculus neftensis (Olexa, 1984), SEM micrographs: 179 – habitus, dorsal view; 180 – ditto, ventral view; 181 – prosternum; 182 – antennal club, ventral view; 183 – ditto, dorsal view; 184 – head, dorsal view; 185 – lateral disc of metaventrite, metepisternum and fused metepimeron; 186 – mesotibia, dorsal view; 187 – protibia, ventral view; 188 – ditto, dorsal view.
Figs. 198–207. Ammostyphrus cerberus Reichardt, 1924 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 198–207. Ammostyphrus cerberus Reichardt, 1924, SEM: 198 – habitus, dorsal view; 199 – ditto, ventral view; 200 – lateral disc of metaventrite, metepisternum and fused metepimeron; 201 – head, dorsal view; 202 – ditto, ventral view; 203 – prosternum; 204 – mentum and cardines and stipites of maxilla, ventral view; 205 – protibia, dorsal view; 206 – metatibia, ventral view; 207 – ditto, dorsal view.
Figs. 168–173 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 168–173. Saprininae, male terminalia, schematic: 168 – 8th sternite, ventral view; 169 – 8th sternite and tergite, dorsal view; 170 – ditto, lateral view; 171 – ninth tergites and tenth tergite, dorsal view; 172 – spiculum gastrale (10th sternite), ventral view; 173 – aedeagus, dorsal view.
Figs. 162–167 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 162–167. Euspilotus (Neosaprinus) perrisi (Marseul, 1872), variability of female pygidial sulci. Figs. 162–165 after OLEXA (1975).
Figs. 45–46 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 45–46. Dorsal structure of labrum showing presence/absence of labral pit and seta (left half showing external and right half showing internal structures): 45 – Hypocaccus (Baeckmanniolus) dimidiatus (Illiger, 1807); 46 – Ctenophilothis chobauti (Théry, 1900).
Figs. 81–89 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 81–89. Saprininae, mandibles, ventral view: 81 – Alienocacculus neftensis (Olexa, 1984); 82 – Ammostyphrus cerberus Reichardt, 1924; 83 – Chalcionellus amoenus (Erichson, 1834); 84 – Chivaenius kryzhanovskii Olexa, 1980; 85 – Ctenophilotis chobauti (Théry, 1900); 86 – Eopachylopus ripae (Lewis, 1885); 87 – Eremosaprinus vlasovi (Reichardt, 1941); 88 – Euspilotus (Neosaprinus) perrisi (Marseul, 1872); 89 – Exaesiopus grossipes grossipes (Marseul, 1855).
Figs. 9–28 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 9–28. Saprininae, sensory structures of the antennal club (vesicles marked with grey; sensory areas shaded): 9 – Saprinus (Saprinus) semistriatus (Scriba, 1790); 10 – Saprinus (Hemisaprinus) subvirescens (Ménétries, 1832); 11 – Myrmetes paykulli Kanaar, 1979; 12 – Styphrus corpulentus Motschulsky, 1845; 13 – Saprinus (Phaonius) pharao (Marseul, 1855); 14 – Ammostyphrus cerberus Reichardt, 1924; 15 – Chalcionellus amoenus (Erichson, 1834); 16 – Chivaenius kryzhanovskii Olexa, 1980; 17 – Ctenophilothis chobauti (Théry, 1900); 18 – Eopachylopus ripae (Lewis, 1885); 19 – Exaesiopus grossipes grossipes (Marseul, 1855); 20 – Hypocaccus (Hypocaccus) rugiceps (Duftschmid, 1805); 21 – Hypocaccus (Baeckmanniolus) dimidiatus dimidiatus (Illiger, 1807); 22 – Hypocacculus (Hypocacculus) metallescens (Erichson, 1834); 23 – Hypocacculus (Colpellus) praecox (Erichson, 1834); 24 – Hypocacculus (Nessus) rubripes (Erichson, 1834); 25 – Paravolvulus lateristrius (Solskij, 1876); 26 – Pholioxenus phoenix (Reichardt, 1930); 27 – Reichardtiolus duriculus (Reitter, 1904); 28 – Xenonychus tridens (Jacquelin-Duval, 1852).
Figs. 39–44 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 39–44. Saprininae, labrum, lateral view: 39 – Philothis (Farabius) hexeris Reichardt, 1930; 40 – Philothis (Atavinus) atavus (Reichardt, 1931); 41 – Saprinus (Phaonius) pharao (Marseul, 1855); 42 – Eremosaprinus vlasovi (Reichardt, 1941); 43 – Ctenophilothis chobauti (Théry, 1900); 44 – Philothis (Philothis) arcanus Reichardt, 1930.
Figs. 144–145. Left maxilla, ventral view. 144 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 144–145. Left maxilla, ventral view. 144 – Eremosaprinus vlasovi (Reichardt, 1941); 145 – Xenophilotis choumovitchi (Thérond, 1965).
Figs. 99–107 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 99–107. Saprininae, mandibles, ventral view: 99 – Philothis (Farabius) hexeris Reichardt, 1930; 100 – Pholioxenus phoenix (Reichardt, 1930); 101 – Reichardtiolus duriculus (Reitter, 1904); 102 – Saprinus (Saprinus) semistriatus (Scriba, 1790); 103 – Saprinus (Hemisaprinus) subvirescens (Ménétries, 1832); 104 – Saprinus (Phaonius) pharao (Marseul, 1855); 105 – Styphrus corpulentus Motschulsky, 1845; 106 – Xenonychus tridens (Jacquelin-Duval, 1852); 107 – Xenophilothis choumovitchi (Thérond, 1965).
Figs. 90–98 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 90–98. Saprininae, mandibles, ventral view: 90 – Gnathoncus rotundatus (Kugelann, 1792); 91 – Hypocaccus (Baeckmanniolus) dimidiatus dimidiatus (Illiger, 1807); 92 – Hypocacculus (Hypocacculus) metalescens (Erichson, 1834); 93 – Hypocacculus (Colpellus) praecox (Erichson, 1834); 94 – Hypocacculus (Nessus) rubripes (Erichson, 1834); 95 – Myrmetes paykulli Kanaar, 1979; 96 – Paravolvulus lateristrius (Solskij, 1876); 97 – Philothis (Philothis) arcanus Reichardt, 1930; 98 – Philothis (Atavinus) atavus (Reichardt, 1931).
Figs. 150–155 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 150–155. Saprininae, legs, schematic: 150 – protibia, ventral view; 151 – ditto, dorsal view; 152 – mesotibia, ventral view; 153 – ditto, dorsal view; 154 – metatibia, ventral view; 155 – ditto, dorsal view.
Figs. 174–178 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 174–178. Variability of the caudal end of spiculum gastrale: 174 – Philothis (Farabius) hexeris Reichardt, 1930; 175 – Hypocacculus (Nessus) rubripes (Erichson, 1834); 176 – Microsaprinus therondianus (Dahlgren, 1973); 177 – Saprinus (Saprinus) semistriatus (Scriba, 1790); 178 – Euspilotus (Neosaprinus) perrisi (Marseul, 1972).
Figs. 79–80 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 79–80. Saprininae, mandibular structures, ventral view: 79 – Hypocaccus (Hypocaccus) rugiceps (Duftschmid, 1805); 80 – Microsaprinus therondianus (Dahlgren, 1973).
Figs. 74–78 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 74–78. Saprininae, labrum, frontal view: 74 – Euspilotus (Neosaprinus) perrisi (Marseul, 1872); 75 – Pholioxenus phoenix (Reichardt, 1930); 76 – Philothis (Atavinus) atavus (Reichardt, 1931); 77 – Philothis (Farabius) hexeris Reichardt, 1930; 78 – Ctenophilothis chobauti (Théry, 1900).
Fig. 116 in Review of the tribes Sogdini and Leiodini from Japan and North Chishima Islands. Part II. Genera Hydnobius and Leiodes (Coleoptera: Leiodidae)
Fig. 116. Distribution of Leiodes. okawai group: broken line – L. okawai Nakane, 1963, (●) L. yukihikoi sp. nov., (■) L. kamezawai sp. nov.
Figs. 47–73 in Review of the Palaearctic genera of Saprininae (Coleoptera: Histeridae)
Figs. 47–73. Saprininae, labral structures, dorsal view (left half showing external and right half showing internal structures): 47 – Alienocacculus neftensis (Olexa, 1984); 48 – Ammostyphrus cerberus Reichardt, 1924; 49 – Chalcionellus amoenus (Erichson, 1834); 50 – Chivaenius kryzhanovskii Olexa, 1980; 51 – Eopachylopus ripae (Lewis, 1885); 52 – Eremosaprinus vlasovi (Reichardt, 1941); 53 – Euspilotus (Neosaprinus) perrisi (Marseul, 1872); 54 – Exaesiopus grossipes grossipes (Marseul, 55); 55 – Gnathoncus rotundatus (Kugelann, 1792); 56 – Hypocaccus (Hypocaccus) rugiceps (Duftschmid, 1805); 57 – Hypocacculus (Hypocacculus) metallescens (Erichson, 1834); 58 – Hypocacculus (Colpellus) praecox (Erichson, 1834); 59 – Hypocacculus (Nessus) rubripes (Erichson, 1834); 60 – Microsaprinus therondianus (Dahlgren, 1973); 61 – Myrmetes paykulli Kanaar, 1979; 62 – Paravolvulus lateristriatus (Solskij, 1876); 63 – Philothis (Philothis) arcanus Reichardt, 1930; 64 – Philothis (Atavinus) atavus (Reichardt, 1931); 65 – Philothis (Farabius) hexeris Reichardt, 1930; 66 – Pholioxenus phoenix (Reichardt, 1930); 67 – Reichardtiolus duriculus (Reitter, 1904); 68 – Saprinus (Saprinus) semistriatus (Scriba, 1790); 69 – Saprinus (Hemisaprinus) subvirescens (Ménétries, 1832); 70 – Saprinus (Phaonius) pharao (Marseul, 1855); 71 – Styphrus corpulentus Motschulsky, 1845; 72 – Xenonychus tridens (Jacquelin-Duval, 1852); 73 – Xenophilothis choumovitchi (Thérond, 1965).
Data archive for the peer-reviewed journal article "Variability in the mass absorption cross-section of black carbon (BC) aerosols is driven by BC internal mixing state at a central European background site (Melpitz, Germany) in winter""
<p>Data archive for figures accompanying the peer-reviewed journal article "Variability in the mass absorption cross-section of black carbon (BC) aerosols is driven by BC internal mixing state at a central European background site (Melpitz, Germany) in winter". In 2020 this article was accepted for publication in the journal <em>Atmospheric Chemistry and Physics</em>. Data are uploaded in the form of Igor Pro experiment files (.pxp).</p>
A complete dietary review of Japanese birds with special focus on molluscs
<p>We present a new database reviewing dietary information for all Japanese bird species. The information within this database was collected through intense literary review to provide a complete look at bird species historically present around the country.</p>
Data accompanying the book review "A new general dictionary of Ume Saami"
<p>This is a set of tables illustrating the differences between two dictionaries of Ume Saami (Schlachter 1958 and Barruk 2018). Headwords with the initial <em>v</em> from both dictionaries have been aligned to show the common and differing shares of vocabulary. A further analysis is published in the book review (Kuokkala 2020) in Finnisch-Ugrische Forschungen (<a href="https://doi.org/10.33339/fuf.99934">doi.org/10.33339/fuf.99934</a>). The data from Schlachter 1958 has been converted into the modern orthography with a script found at <a href="https://doi.org/10.5281/zenodo.4162535">doi.org/10.5281/zenodo.4162535</a> and published in its entirety at <a href="https://doi.org/10.5281/zenodo.4163676">doi.org/10.5281/zenodo.4163676</a>.</p>
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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.