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.
1,736
datasets available to search
ShareScore release 0.7.1
Dataset results
1,736 results for “Coleoptera: Tenebrionidae”
Figure 1 in Research on Alleculinae (Coleoptera: Tenebrionidae: Alleculinae) in tugai forests of the Almaty region in Kazakhstan using window traps
Figure 1. Shelek. Window trap on stem of Populus pruinosa in tugai forest – habitat of Steneryx dejeani occurrence. Photo by Oto Nakládal.
Figure 3 in First record of the saproxylic beetle Corticeus (= Hypophloeus) unicolor Piller & Mitterpacher, 1783 in Montenegro (Coleoptera: Tenebrionidae) with comments on old-growth forests conservation in the Country
Figure 3. Mixed beech–silver fir–Norway spruce old-growth forest, snag and coarse woody debrys in Biogradska gora National Park, where Corticeus unicolor was collected.
Figure 2 in First record of the saproxylic beetle Corticeus (= Hypophloeus) unicolor Piller & Mitterpacher, 1783 in Montenegro (Coleoptera: Tenebrionidae) with comments on old-growth forests conservation in the Country
Figure 2. Corticeus unicolor: (A) side view and (B) view from above (B). Scale bar: 1 mm. Photos by F. Parisi.
Figure 1. A in Further finding of Bolitophagus reticulatus (Linnaeus, 1767) in Montenegro (Coleoptera: Tenebrionidae) with brief comments on its distribution and conservation
Figure 1. A. Location of Bolitophagus reticulatus finding site in Montenegro. B. Localization of the finding in the Bjelasica mountain range in the Dinaric Alps (Montenegro). Graphic processing Giovanni D'Amico.
Figure 2 in Further finding of Bolitophagus reticulatus (Linnaeus, 1767) in Montenegro (Coleoptera: Tenebrionidae) with brief comments on its distribution and conservation
Figure 2. Mixed forest of Norwegian beech-fir and fallen dead trees in Biogradska Gora National Park, where Bolitophagus reticulatus was found. Photo by F. Parisi.
Figure 3 in Further finding of Bolitophagus reticulatus (Linnaeus, 1767) in Montenegro (Coleoptera: Tenebrionidae) with brief comments on its distribution and conservation
Figure 3. Specimen of Bolitophagus reticulatus collected in Biogradska Gora National Park. Scale bar: 1 mm. The specimen was photographed with a 3D microscope with a full HD camera and LED illumination. Photo by F. Parisi.
Fig. 3 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions
Fig. 3. Mean body weight of larvae (mg) fed 30,000 and 50,000 ppm of volcanic ash treated flour disks afer 15 d. Bars with the same letter are not significantly different α = 0.05. Bioassay endpoint = 15 d, n = 10, substrate = treated and control insect food (ANOVA: F = 93.67; df = 2; P <0.0001).
Fig. 1 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions
Fig. 1. Chemical composition of ash from Puyehue Cordon Caulle eruption collected in Collón Curá, Neuquén, Argentina (40.0400°S, 70.2405°W) 15 Jun 2011, determined by energy dispersive spectroscopy. Previously published in Buteler et al. (2011), Revista de la Sociedad Entomológica Argentina 70 (3–4), Figure 3, copyright RSEA, reproduced with permission.
Fig. 6 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions
Fig. 6. Molting rate of Tenebrio molitor larvae feed on flour disks treated with sub-lethal concentrations (500, 1,000, 5,000 ppm) of volcanic ash. Molting rate = number of molts per incubation period of 27 d.
Fig. 5 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions
Fig. 5. Larval body length (cm) of Tenebrio molitor larvae fed on flour disks treated with sub-lethal concentrations (500, 1,000, 5,000 ppm) of volcanic ash. Bars with the same letter are not significantly different α = 0.05. Bioassay endpoint = 27 d, n = 10, substrate = treated and control insect food (ANOVA: F = 95.15; df = 3; P <0.0001).
Fig. 4 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions
Fig. 4. Mean body weight of larvae (mg) fed on sub lethal concentrations (500, 1,000, 5,000 ppm) of volcanic ash treated flour disks. Bars with the same letter are not significantly different at α = 0.05. Bioassay endpoint = 27 d, n = 10, substrate = treated and control insect food (ANOVA: F = 133.97; df = 3; P <0.0001).
Figs 29–33 in Taxonomic review of the genus Helops Fabricius, 1775 (Coleoptera: Tenebrionidae) of Turkey
Figs 29–33. Helops glabriventris glabriventris, male genitalia and terminalia. 29 – aedeagus, ventral view; 30 – median piece (penis); 31 – aedeagus, lateral view; 32 – lobe of gastral spicula, lateral view; 33 – male inner sternite VIII, ventrally. Рис. 29–33. Helops glabriventris glabriventris, генитаΛии и терминаΛии самца. 29 – эΑеагус вентраΛьно; 30 – пенис; 31 – эΑеагус ΛатераΛьно; 32 – Λопасть гастраΛьной спикуΛы, ΛатераΛьно; 33 – VIII внутренний стернит самца, вентраΛьно.
Figs 24–28 in Taxonomic review of the genus Helops Fabricius, 1775 (Coleoptera: Tenebrionidae) of Turkey
Figs 24–28. Helops rossii, male genitalia and terminalia. 24 – aedeagus, ventral view; 25 – median piece (penis); 26 – aedeagus, lateral view; 27 – lobe of gastral spicula, lateral view; 28 – male inner sternite VIII, dorsally. Рис. 24–28. Helops rossii, генитаΛии и терминаΛии самца. 24 – эΑеагус вентраΛьно; 25 – пенис; 26 – эΑеагус ΛатераΛьно; 27 – Λопасть гастраΛьной спикуΛы, ΛатераΛьно; 28 – VIII внутренний стернит самца, ΑорсаΛьно.
Figs 1–6. Helops spp., habitus. 1 – H in Taxonomic review of the genus Helops Fabricius, 1775 (Coleoptera: Tenebrionidae) of Turkey
Figs 1–6. Helops spp., habitus. 1 – H. caeruleus stevenii, male; 2 – the same, female; 3 – H. rossii, male; 4 – the same, female; 5 – H. glabriventris glabriventris, male; 6 – the same, female. Рис. 1–6. Helops spp., габитус. 1 – H. caeruleus stevenii, самец; 2 – то же, самка; 3 – H. rossii, самец; 4 – то же, самка; 5 – H. glabriventris glabriventris, самец; 6 – то же, самка.
Figs 39–43 in Taxonomic review of the genus Helops Fabricius, 1775 (Coleoptera: Tenebrionidae) of Turkey
Figs 39–43. Helops punctatissimus sp. n., male genitalia and terminalia. 39 – aedeagus, ventral view; 40 – median piece (penis); 41 – aedeagus, lateral view; 42 – male inner sternite VIII, ventrally; 43 – gastral spicula. Рис. 39–43. Helops punctatissimus sp. n., генитаΛии и терминаΛии самца. 39 – эΑеагус вентраΛьно; 40 – пенис; 41 – эΑеагус ΛатераΛьно; 42 – VIII внутренний стернит самца, вентраΛьно; 43 – гастраΛьная спикуΛа.
Figs 19–23 in Taxonomic review of the genus Helops Fabricius, 1775 (Coleoptera: Tenebrionidae) of Turkey
Figs 19–23. Helops caeruleus sevenii, male genitalia and terminalia. 19 – aedeagus, ventral view; 20 – median piece (penis); 21 – aedeagus, lateral view; 22 – lobe of gastral spicula, lateral view; 23 – male inner sternite VIII, ventrally. Рис. 19–23. Helops caeruleus sevenii, генитаΛии и терминаΛии самца. 19 – эΑеагус вентраΛьно; 20 – пенис; 21 – эΑеагус ΛатераΛьно; 22 – Λопасть гастраΛьной спикуΛы, ΛатераΛьно; 23 – VIII внутренний стернит самца, вентраΛьно.
Figs 34–38 in Taxonomic review of the genus Helops Fabricius, 1775 (Coleoptera: Tenebrionidae) of Turkey
Figs 34–38. Helops cyanipes, male genitalia and terminalia. 34 – aedeagus, ventral view; 35 – median piece (penis); 36 – aedeagus, lateral view; 37 – lobe of gastral spicula, lateral view; 38 – male inner sternite VIII, ventrally. Рис. 34–38. Helops cyanipes, генитаΛии и терминаΛии самца. 34 – эΑеагус вентраΛьно; 35 – пенис; 36 – эΑеагус ΛатераΛьно; 37 – Λопасть гастраΛьной спикуΛы, ΛатераΛьно; 38 – VIII внутренний стернит самца, вентраΛьно.
Figs 7–18 in Taxonomic review of the genus Helops Fabricius, 1775 (Coleoptera: Tenebrionidae) of Turkey
Figs 7–18. Helops spp., habitus, details of structure. 7 – H. cyanipes, male, habitus (Çamlıyayla, Mersin Province); 8 – the same, female (south of Hatay Province); 9 – H. punctatissimus sp. n., male; 10 – H. caeruleus stevenii, head; 11 – H. punctatissimus sp. n., head; 12 – H. cyanipes, punctation of metatibia; 13 – H. punctatissimus sp. n., the same; 14–18 – punctation and sculpture of elytra: 14 – H. caeruleus stevenii, 15 – H. rossii, 16 – H. glabriventris glabriventris, 17 – H. cyanipes, 18 – H. punctatissimus sp. n. Рис. 7–18. Helops spp., габитус, ÃетаΛи строения. 7 – H. cyanipes, самец, габитус (ЧамΛыяйΛа, провинция Мерсин); 8 – то же, самка (юг провинции Хатай); 9 – H. punctatissimus sp. n., самец; 10 – H. caeruleus stevenii, гоΛова; 11 – H. punctatissimus sp. n., гоΛова; 12 – H. cyanipes, пунктировка заÃней гоΛени; 13 – H. punctatissimus sp. n., то же; 14–18 – пунктировка и скуΛьптура наÃкрыΛий: 14 – H. caeruleus stevenii, 15 – H. rossii, 16 – H. glabriventris glabriventris, 17 – H. cyanipes, 18 – H. punctatissimus sp. n.
Fig. 4 in The effects of three essential oils on adult repellency, larval fumigant toxicity, and egg hatch of Tribolium castaneum (Coleoptera: Tenebrionidae)
Fig. 4. Mean red flour beetle egg hatch (± SE) during exposure to rice grains treated with 1 of 3 essential oils at varying exposure times. Means with a different letter for each time interval are significantly different (Tukey's HSD post hoc test, P <0.05).
Fig. 3 in The effects of three essential oils on adult repellency, larval fumigant toxicity, and egg hatch of Tribolium castaneum (Coleoptera: Tenebrionidae)
Fig. 3. Mean percent (± SE) repellency of adult red flour beetles at varying intervals of exposure, tested separately to 1 of 3 essential oils. Means with a different letter for each time interval are significantly different (Tukey's HSD post hoc test, P <0.05).
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.