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.
1,694
datasets available to search
ShareScore release 0.7.1
Dataset results
1,694 results for “weevils”
Figs. 37– 41. Coconotus tuberculatus Anderson and Lanteri. 37 in New Genera and Species of Weevils from the Galapagos Islands, Ecuador, and Cocos Island, Costa Rica (Coleoptera; Curculionidae; Entiminae; Entimini)
Figs. 37– 41. Coconotus tuberculatus Anderson and Lanteri. 37, female abdomen, ventral view; 38, sternite 8; 39, tergites 7 and 8; 40, hemisternites, 41, spermatheca. Scale line = 1 mm, except spermatheca = 0.25 mm.
Fig. 5 in METAPOCYRTUS MADAYAW SP. N. (COLEOPTERA: CURCULIONIDAE, ENTIMINAE), A NEW FLIGHTLESS WEEVIL FROM EASTERN MINDANAO, PHILIPPINES
Fig. 5. Habitats of Metapocyrtus (Artapocyrtus) madayaw sp. n. A – Lamiawan, Davao Oriental; B – Maragusan, Davao de Oro.
Рис. 5–10. Otiorhynchus paradigitalis sp. n., общий виΑ и ΑетаΛи строения. 5 –самец, гоΛотип; 6 – самка, паратип; 7 – эΑеагус; 8 – сперматека; 9 – spiculum ventrale; 10 – кокситы. Figs 5–10. Otiorhynchus paradigitalis sp. n., general view and details of structure. 5 – male, holotype; 6 – female, paratype; 7 – aedeagus; 8 – spermatheca; 9 – spiculum ventrale; 10 – coxites. in A new weevil of the subgenus Otismotilus Reitter, 1912, genus Otiorhynchus Germar, 1824 (Coleoptera: Curculionidae: Entiminae) from the Caucasus
Рис. 5–10. Otiorhynchus paradigitalis sp. n., общий виΑ и ΑетаΛи строения. 5 –самец, гоΛотип; 6 – самка, паратип; 7 – эΑеагус; 8 – сперматека; 9 – spiculum ventrale; 10 – кокситы. Figs 5–10. Otiorhynchus paradigitalis sp. n., general view and details of structure. 5 – male, holotype; 6 – female, paratype; 7 – aedeagus; 8 – spermatheca; 9 – spiculum ventrale; 10 – coxites.
Рис. 1–4. Otiorhynchus digitalis Yunakov et Davidian, 2002, самка, гоΛотип. 1 – общий виΑ; 2 – кокситы; 3 – сперматека; 4 – spiculum ventrale. Figs 1–4. Otiorhynchus digitalis Yunakov et Davidian, 2002, female, holotype. 1 – general view; 2 – coxites; 3 – spermatheca; 4 – spiculum ventrale. in A new weevil of the subgenus Otismotilus Reitter, 1912, genus Otiorhynchus Germar, 1824 (Coleoptera: Curculionidae: Entiminae) from the Caucasus
Рис. 1–4. Otiorhynchus digitalis Yunakov et Davidian, 2002, самка, гоΛотип. 1 – общий виΑ; 2 – кокситы; 3 – сперматека; 4 – spiculum ventrale. Figs 1–4. Otiorhynchus digitalis Yunakov et Davidian, 2002, female, holotype. 1 – general view; 2 – coxites; 3 – spermatheca; 4 – spiculum ventrale.
Рис. 11. Распространение Otiorhynchus digitalis Yunakov et Davidian, 2002 (круг) и O. paradigitalis sp. n. (кваΑрат). Fig 11. Distribution of Otiorhynchus digitalis Yunakov et Davidian, 2002 (circle) and O. paradigitalis sp. n. (square). in A new weevil of the subgenus Otismotilus Reitter, 1912, genus Otiorhynchus Germar, 1824 (Coleoptera: Curculionidae: Entiminae) from the Caucasus
Рис. 11. Распространение Otiorhynchus digitalis Yunakov et Davidian, 2002 (круг) и O. paradigitalis sp. n. (кваΑрат). Fig 11. Distribution of Otiorhynchus digitalis Yunakov et Davidian, 2002 (circle) and O. paradigitalis sp. n. (square).
FIG. 7 in Rediscovery of the wingless Podolian subendemic weevil Humeromima rufipes (Boheman, 1834) (Coleoptera, Curculionidae, Entiminae), a relict from the Last Glacial Maximum
FIG. 7. — Alpha-diversity characteristics of the grass litter Entiminae community (Humeromima rufipes (Boheman, 1834) and co-occurring species) in Western Podolia: A, evenness of the community evaluated using Shannon and Simpson indices; B, top 10 grass litter Entiminae species in Western Podolia. Abbreviations: Invsimpson, 1/Simpson (inverted Simpson); n, the total number of specimens per sample; Sobs, the number of observed species.
FIG. 6 in Rediscovery of the wingless Podolian subendemic weevil Humeromima rufipes (Boheman, 1834) (Coleoptera, Curculionidae, Entiminae), a relict from the Last Glacial Maximum
FIG. 6. — Habitats of Humeromima rufipes (Boheman, 1834): A, meadow steppe, near Burshtyn, Kasova Hora, IFR; B, rock steppe, near Buchyna, Mts. Drancha, LWI; C, rock steppe, near Kuropatnyky, IFR; D, grass steppe, near Kyikiv, LWI; E, meadow steppe, near Mokrotyn, Mt. Harai, LWI; F, meadow steppe, Yaktoriv, Mt. Chekhova, LWI.
FIG. 4 in Rediscovery of the wingless Podolian subendemic weevil Humeromima rufipes (Boheman, 1834) (Coleoptera, Curculionidae, Entiminae), a relict from the Last Glacial Maximum
FIG. 4. — Humeromima rufipes (Boheman, 1834), morphology, female (27365, Mt. Chekhova): A, head, dorsal view; B, head, lateral view; C, head, ventral view; D, scales of elytra; E, maxilla; F, labium, ventral view; G, labium, lateral view; H, antenna; I, head, (cleared specimen); J, fore leg; K, middle leg; L, hind leg; M, tarsus, dorsal and lateral; N, mesonotum; O, coxal cavities, ventral view; P, coxal cavities, lateral view; Q, sterna of pterothorax and ventrites (cleared specimen). Abbreviations: as-am, anterior margin of antennal scrobes; la-te, lacinial teeth; li, ligula; li-ca, cavity of ligula; ocs, occipital sutures; pp, prosternal process; pr, prosternellum; pta, posterior tentorial arms; ptp, posterior tentorial pits; tm3-lo, tarsomere 3 lobes. Scale bars:A-C, H, J-O, 200 µm; D, µm; E-G, 50 µm; I, Q, 300 µm.
FIG. 5 in Rediscovery of the wingless Podolian subendemic weevil Humeromima rufipes (Boheman, 1834) (Coleoptera, Curculionidae, Entiminae), a relict from the Last Glacial Maximum
FIG. 5. — Humeromima rufipes (Boheman, 1834), morphology: A, aedeagus, lateral view; B, aedeagus, dorsal view; C, male sternite 8; D, male sternite 8 and 9; E, endophallus armatute; F, female terminalia; G, female sternite 8 and ovipositor; H, apical part of female terminalia (magnified); I, spermatheca. Abbreviations: buc, bursa copulatrix; co, collum; co-mf, membranous formation in apical half of collum; dp, dorsal plate; ds, ductus spermaticus; es, endophallic sclerite; fst8-ap, apodeme of female sternite 8; fst8-lm, lamina of female sternite 8; fst8-se, setae of female sternite 8; lov, lateral ostial valves; ml-al, apical lobes of median lobe; ml-amp, apical membranous plate of median lobe; ml-ap, apodemes of median lobe; ml-app, apical preostial process; mst8, male sternite 8; mst9-ca, caput of apodeme of sternite 9; no, nodulus (= corpus); oss, ostial sclerite; ra, ramus; sg, spermathecal gland; ut, uterus; va, vagina. Scale bars: A, B, 100 µm; C, E, I, 50 µm; D, F-H, 200 µm; I, Q, 300 µm.
FIG. 3 in Rediscovery of the wingless Podolian subendemic weevil Humeromima rufipes (Boheman, 1834) (Coleoptera, Curculionidae, Entiminae), a relict from the Last Glacial Maximum
FIG. 3. — Humeromima rufipes (Boheman, 1834): A, dorsal, ventral, lateral habitus of female (27761, Luka); B, dorsal, ventral, lateral habitus of male (27732, 0.5 km E Kyikiv). Scale bar: 1 mm.
FIG. 1 in Rediscovery of the wingless Podolian subendemic weevil Humeromima rufipes (Boheman, 1834) (Coleoptera, Curculionidae, Entiminae), a relict from the Last Glacial Maximum
FIG. 1. — Distribution of Humeromima rufipes (Boheman, 1834): A, occurrences plotted as heat points, alongside paleoenvironmental data for central Europe; B, extent of occurrence (EOO) and Area of occupancy (AOO); C, temporal plot of occurrence data showing the number of years since the last collection of H. rufipes in each historic locality.
FIG. 2 in Rediscovery of the wingless Podolian subendemic weevil Humeromima rufipes (Boheman, 1834) (Coleoptera, Curculionidae, Entiminae), a relict from the Last Glacial Maximum
FIG. 2. — Humeromima rufipes (Boheman, 1834): A, lectotype, male, habitus dorsal, lateral, ventral view and labels. Photo credit: by Anna Jerve (NHRS); B, habitus of historical specimen (male) from most remote location in Romania. Photo credit: by Kevin Weissing (SDEI). Scale bars: 1 mm.
Fig. 3 in METAPOCYRTUS MADAYAW SP. N. (COLEOPTERA: CURCULIONIDAE, ENTIMINAE), A NEW FLIGHTLESS WEEVIL FROM EASTERN MINDANAO, PHILIPPINES
Fig. 3. Metapocyrtus (Artapocyrtus) spp. A, B – M. (A.) pardalis Heller, 1912 (female paratype): A – rostrum, dorsal view, B – same, lateral view; C, D – M. (A.) madayaw sp. n.: C – rostrum, dorsal view; D – idem, lateral view.
Fig. 2 in METAPOCYRTUS MADAYAW SP. N. (COLEOPTERA: CURCULIONIDAE, ENTIMINAE), A NEW FLIGHTLESS WEEVIL FROM EASTERN MINDANAO, PHILIPPINES
Fig. 2. Metapocyrtus (Artapocyrtus) spp. A, B – M. (A.) pardalis Heller, 1912: A – female type, dorsal view, B – same, lateral view; C, D – M. (A.) madayaw sp. n.: C – female paratype, dorsal view; D – same, lateral view.
Fig. 1 in METAPOCYRTUS MADAYAW SP. N. (COLEOPTERA: CURCULIONIDAE, ENTIMINAE), A NEW FLIGHTLESS WEEVIL FROM EASTERN MINDANAO, PHILIPPINES
Fig. 1 Metapocyrtus (Artapocyrtus) madayaw sp. n. A – male holotype, dorsal view; B – female paratype, dorsal view; C – male holotype, lateral view; D – female paratype, lateral view.
Fig. 4 in METAPOCYRTUS MADAYAW SP. N. (COLEOPTERA: CURCULIONIDAE, ENTIMINAE), A NEW FLIGHTLESS WEEVIL FROM EASTERN MINDANAO, PHILIPPINES
Fig. 4. Metapocyrtus (Artapocyrtus) madayaw sp. n., aedeagus. A – dorsal view; B – lateral view; C – sternite IX in dorsal view.
Responsiveness of the broad bean weevil Bruchus rufimanus Boh. to different Vicia faba L. genotypes
<p><span>The broad bean weevil <em>Bruchus rufimanus</em> Boh., also called bruchid beetle, is a major pest of Vicia faba L. given that larvae develop inside the seeds causing direct quality losses in agricultural products. Recurrent chemical applications are inappropriate because they represent a serious threat to pollinators in general. In addition, biological control approaches that have been attempted so far showed limited effectiveness, which makes studies of methods to control bruchid populations extremely important. Breeding resistant cultivars is the most adequate approach to achieve efficient levels of pest resistance and promote sustainable agriculture. To explore the mechanisms underlying bruchid resistance, we explored B. rufimanus behavior in different life stages and plant preference in feeding, oviposition and larval survival into adulthood both in greenhouse experiments and in the field. Our greenhouse results showed that females, compared to males, have preferences for flowers from some genotypes over the others although the choices made did not correspond with the laying preference. The egg laying preference of females was significantly affected by cultivars. This attraction could be explained by the number of seeds per pod produced by the genotypes, while in the field flowering time influenced bruchid infestation. Moreover, the survival of the larva into adulthood was greater in certain genotypes over the others. The results of our study lay the groundwork for further analyses to finely dissect V. faba resistance towards bruchids and pave the way for the development of methods to predict potential resistant genotypes in research and breeding programs.</span></p>
Fig. 4 in Yagder serratus, a new eyeless weevil from Mexico and the non-monophyly of Brachycerinae, the evolutionary twilight zone of true weevils (Coleoptera: Curculionidae)
Fig. 4. Eyeless and nearly eyeless brachycerine weevils, habitus. A tip of a regular mechanical pencil with a 0.5 mm lead is added for size comparison. All images are to scale.
Fig. 2 in Yagder serratus, a new eyeless weevil from Mexico and the non-monophyly of Brachycerinae, the evolutionary twilight zone of true weevils (Coleoptera: Curculionidae)
Fig. 2. Yagder serratus gen. & sp. nov., details. A–C – rostral apex, dorsal (A), left lateral (B), ventral (C); D – head, left lateral; E–F – left antenna, lateral (E), distal part magnified (F); G–I – tarsi, left front leg (G–H), left middle leg (I); J – elytral apex; K–L – dissected female abdominal apex, ventral (K) and right latero-ventral (L).
Fig. 5 in Yagder serratus, a new eyeless weevil from Mexico and the non-monophyly of Brachycerinae, the evolutionary twilight zone of true weevils (Coleoptera: Curculionidae)
Fig. 5. Eyeless and nearly eyeless brachycerine weevils, details. A – Alaocyba sp. (10826), anterior body, left lateral; B – Homosomus depressus Richard, 1979, anterior body, left lateral; C – Raymondiellus sp. (10827), left middle leg, anterior; D – Bordoniola sp. (10330), left antenna, lateral; E – Bordoniola sp. (10331), head, left lateral; F – Himasthlophallus flagellifer Egorov & Zherikhin, 1991, anterior body, left lateral.
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.