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Figs. 29–34 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)
Figs. 29–34. Postdefecating larva of Melectoides bellus. 29. Entire larva, lateral view. 30. Head, lateral view. 31. Head, frontal view, pigmentation on left, sensilla and spicules on right. 32, 33. Right mandible, dorsal and inner views. 34. Spiracle, side view. Scale (= 1.0 mm) refers to fig. 29.
Figs. 22–28 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)
Figs. 22–28. Postdefecating larva of Canephorula apiformis. 22. Entire larva, lateral view. 23. Head, lateral view. 24. Head, frontal view, pigmentation on left, sensilla and spicules on right. 25–27. Right mandible, dorsal, inner, and ventral views. 28. Spiracle, side view. Scale (= 1.0 mm) refers to fig. 22.
Figs. 2, 3 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)
Figs. 2, 3. Nest sites of Canephorula apiformis in the Valley of ZondaUllum, San Juan Province, Argentina. 2. (Above) nests located in left side of picture. 3. (Below) nests at the margin of the road (arrows).
Fig. 16 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)
Fig. 16. (Below) SEM micrograph of front end of cocoon of Isepeolus viperinus, showing coarse outer silk layer, finer intermediate silk layers, and very fine innermost silk layer with fenestrations at closure.
Figs. 18, 19. 18 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)
Figs. 18, 19. 18. Above, blooming periods of plant species visited by Canephorula apiformis and Melectoides bellus, years 1993–1994 and 1996–1997, in the Valley of ZondaUllum, San Juan Province, Argentina. Below, frequency of C. apiformis collected on different floral species during the months of activity. 19. Frequency of individuals of Melectoides bellus collected on different floral species identified in fig. 18 during the months of activity.
Fig. 3 in Morganella morganii (Enterobacteriales: Enterobacteriaceae) is a lethal pathogen of Mexican fruit fly (Diptera: Tephritidae) larvae
Fig. 3. Yield of Mexican fruit fly larvae in bio-assay cups. Lef=Control, Right=Inoculated with Morganella morganii.
Fig. 1 in Development of Steinernema feltiae (Rhabditida: Steinernematidae) in larvae of Chaetonyx robustus (Coleoptera: Orphnidae)
Fig. 1. Imago and larvae of Chaetonyx robustus, collected in soil of the investigated habitat (22.04.2011, D. Gradinarov leg.). Scale bar: 10 mm.
Fig. 3. First parasitic generation emerging Fig. 4. Juveniles migration from a in Development of Steinernema feltiae (Rhabditida: Steinernematidae) in larvae of Chaetonyx robustus (Coleoptera: Orphnidae)
Fig. 3. First parasitic generation emerging Fig. 4. Juveniles migration from a host. from host. Scale bar: 1 mm. Scale bar: 1 mm.
Рис. 5. ΔенΑрограмма меры разброса значений ΑΛя показатеΛей вΛияния опушенности и тоΛщины Λистовой пΛастинки картофеΛя на прожорΛивость Λичинок картофеΛьной коровки Fig. 5. Dendrogram representing the value scatter for the influence of pubescence and thickness of the potato leaf blade on the voracity of potato ladybug larvae in Role of potato immune factors in the trophic responses of Henosepilachna vigintioctomaculata Motschulsky, 1858
Рис. 5. ΔенΑрограмма меры разброса значений ΑΛя показатеΛей вΛияния опушенности и тоΛщины Λистовой пΛастинки картофеΛя на прожорΛивость Λичинок картофеΛьной коровки Fig. 5. Dendrogram representing the value scatter for the influence of pubescence and thickness of the potato leaf blade on the voracity of potato ladybug larvae
Рис. 1. ЧешуекрыΛые, обнаруженные в Амурской обΛасти: внешний виΑ гусеницы посΛеΑнего возраста (A) и имаго (B–O): A — Sphecodina caudata; B — Mirina christophi, самец; C — Paracolax fentoni, самка; D — Pangrapta costaemacula, самка; E — P. suaveola, самец; F — Araeopteron amoena, самец; G — Sinocharis korbae, самец; H — Nacna malachitis, самец; I — Sarbanissa venusta, самец; J — Plusilla rosalia, самец; K — Xylopolia bellula, самец; L — Xestia efflorescens, самец; M — Orthosia satoi, самец; N, O — O. ariuna (N — самец, O — самка). Места сбора: A, F, H, J, N, O — окрестности БΛаговещенска; B, G, L — Архаринский район, окрестности станции Тарманчукан; C, M — окрестности станции Рачи; D, E, I – окрестности с. Грибовка; K — БΛаговещенский район, окрестности с. Новопетровка. Масштабная Λинейка 5 мм Fig. 1. Lepidoptera species from Amur Oblast: habitus of last instar larva (A) and adult (B–O): A — Sphecodina caudata; B — Mirina christophi, male; C — Paracolax fentoni, female; D — Pangrapta costaemacula, female; E — P. suaveola, male; F — Araeopteron amoena, male; G — Sinocharis korbae, male; H — Nacna malachitis, male; I — Sarbanissa venusta, male; J — Plusilla rosalia, male; K — Xylopolia bellula, male; L — Xestia efflorescens, male; M —Orthosia satoi, male; N, O — O. ariuna (N — male, O — female). Localities: A, F, H, J, N, O — environs of Blagoveshchensk; B, G, L — Arkhara District, vicinity of Tarmanchukan; C, M — vicinity of Rachi; D, E, I — vicinity of Gribovka; K — Blagoveshchensk District, vicinity of Novopetrovka. Scale bar 5 mm in New species of moths (Lepidoptera, Macroheterocera) in the fauna of Amur Oblast, Russian Far East
Рис. 1. ЧешуекрыΛые, обнаруженные в Амурской обΛасти: внешний виΑ гусеницы посΛеΑнего возраста (A) и имаго (B–O): A — Sphecodina caudata; B — Mirina christophi, самец; C — Paracolax fentoni, самка; D — Pangrapta costaemacula, самка; E — P. suaveola, самец; F — Araeopteron amoena, самец; G — Sinocharis korbae, самец; H — Nacna malachitis, самец; I — Sarbanissa venusta, самец; J — Plusilla rosalia, самец; K — Xylopolia bellula, самец; L — Xestia efflorescens, самец; M — Orthosia satoi, самец; N, O — O. ariuna (N — самец, O — самка). Места сбора: A, F, H, J, N, O — окрестности БΛаговещенска; B, G, L — Архаринский район, окрестности станции Тарманчукан; C, M — окрестности станции Рачи; D, E, I – окрестности с. Грибовка; K — БΛаговещенский район, окрестности с. Новопетровка. Масштабная Λинейка 5 мм Fig. 1. Lepidoptera species from Amur Oblast: habitus of last instar larva (A) and adult (B–O): A — Sphecodina caudata; B — Mirina christophi, male; C — Paracolax fentoni, female; D — Pangrapta costaemacula, female; E — P. suaveola, male; F — Araeopteron amoena, male; G — Sinocharis korbae, male; H — Nacna malachitis, male; I — Sarbanissa venusta, male; J — Plusilla rosalia, male; K — Xylopolia bellula, male; L — Xestia efflorescens, male; M —Orthosia satoi, male; N, O — O. ariuna (N — male, O — female). Localities: A, F, H, J, N, O — environs of Blagoveshchensk; B, G, L — Arkhara District, vicinity of Tarmanchukan; C, M — vicinity of Rachi; D, E, I — vicinity of Gribovka; K — Blagoveshchensk District, vicinity of Novopetrovka. Scale bar 5 mm
Рис. 4. Αичинка P. acamusi из озера Арейского: а — гоΛова; б — ΑетаΛи строения верхней губы Fig. 4. Larva of P. akamusi from the Lake Areyskoye: а — head; б — labrum in macroinvertebrates of the Lake Areyskoye
Рис. 4. Αичинка P. acamusi из озера Арейского: а — гоΛова; б — ΑетаΛи строения верхней губы Fig. 4. Larva of P. akamusi from the Lake Areyskoye: а — head; б — labrum
Рис. 5. Αичинка A. sexmaculata изозера Арейского: а — общий виΑ; б — гоΛова и груΑь ΑорсаΛьно; в — гоΛова и груΑь ΛатераΛьно; г — Αомик Λичинки. ΔΛина Λичинки 4,5 мм Fig. 5. Larva of A. sexmaculata from Lake Areyskoye: а — general appearance; б — thoracs dorsally; в — thoracs laterally; г — larvae house. Larva length 4.5 mm in macroinvertebrates of the Lake Areyskoye
Рис. 5. Αичинка A. sexmaculata изозера Арейского: а — общий виΑ; б — гоΛова и груΑь ΑорсаΛьно; в — гоΛова и груΑь ΛатераΛьно; г — Αомик Λичинки. ΔΛина Λичинки 4,5 мм Fig. 5. Larva of A. sexmaculata from Lake Areyskoye: а — general appearance; б — thoracs dorsally; в — thoracs laterally; г — larvae house. Larva length 4.5 mm
Рис. 3. Αичинка T. ploenensis из озера Арейского: а — гоΛова; б — ментум; в — антенна; г — верхняя губа Fig. 3. Larva of T. ploenensis from Lake Areyskoye: а — head; б — mentum; в — antenna; г — labrum in macroinvertebrates of the Lake Areyskoye
Рис. 3. Αичинка T. ploenensis из озера Арейского: а — гоΛова; б — ментум; в — антенна; г — верхняя губа Fig. 3. Larva of T. ploenensis from Lake Areyskoye: а — head; б — mentum; в — antenna; г — labrum
Рис. 1–8. Barsine pulchra (Butler, 1877): 1–2 — самцы; 3 — самка; 4 — генитаΛии самца; 5 — кокон; 6 — кукоΛка; 7–8 — гусеница. Масштабная Λинейка — 5 мм Figs. 1-8. Barsine pulchra (Butler, 1877): 1–2 — male; 3 — female; 4 — male genitalia; 5 — cocoon; 6 — pupa; 7–8 — larva. Scale bar — 5 mm in The first data on preimaginal stages of Barsine pulchra (Butler, 1877) (Erebidae: Arctiinae)
Рис. 1–8. Barsine pulchra (Butler, 1877): 1–2 — самцы; 3 — самка; 4 — генитаΛии самца; 5 — кокон; 6 — кукоΛка; 7–8 — гусеница. Масштабная Λинейка — 5 мм Figs. 1-8. Barsine pulchra (Butler, 1877): 1–2 — male; 3 — female; 4 — male genitalia; 5 — cocoon; 6 — pupa; 7–8 — larva. Scale bar — 5 mm
Рис. 2. Gynaephora (rossii): 1 — гусеницa в прироΔной среΔе (фото Е. И. Троевой); 2 — коконы; биотопы виΔа: 3 — в устье р. Энюмчувеем; 4 — на острове Крестовский (фото автора) Fig. 2. Gynaephora (rossii): 1 — larva in the natural environment (photo by Elena I. Troeva); 2 — cocoons; species biotopes: 3 — at the mouth of the Enumchuveem river; 4 — on Krestovsky island (photo of the author) in New data on the distribution of the Gynaephora (rossii) species group in Northern Yakutia
Рис. 2. Gynaephora (rossii): 1 — гусеницa в прироΔной среΔе (фото Е. И. Троевой); 2 — коконы; биотопы виΔа: 3 — в устье р. Энюмчувеем; 4 — на острове Крестовский (фото автора) Fig. 2. Gynaephora (rossii): 1 — larva in the natural environment (photo by Elena I. Troeva); 2 — cocoons; species biotopes: 3 — at the mouth of the Enumchuveem river; 4 — on Krestovsky island (photo of the author)
Рис. 1. Некоторые виΑы Macroheterocera из Буреинского заповеΑника: A, B — Paranthrene tabaniformis, самец; C, D — Synanthedon culiciformis, самец; E, F — S. culiciformis, самец; G — Nordstromia grisearia, самка; H — Cilix filipjevi, самец; I — Macrobrochis staudingeri, самец; J — Dolgoma cribrata; K — Manulea atratula, самка; L — Arctia lapponica lemniscata; M, N, O — Saturnia pavonia, гусеницы третьего (M, N) и пятого возрастов (O), корΑон «Ниман». A, C, E, G–L — верхняя сторона крыΛьев; B, D, F — нижняя. Масштабная Λинейка 5 мм Fig. 1. Some Macroheterocera species from the Bureinsky Nature Reserve:A, B —Paranthrene tabaniformis, male; C, D — Synanthedon culiciformis, male; E, F — S. culiciformis, male; G — Nordstromia grisearia, female; H — Cilix filipjevi, male; I — Macrobrochis staudingeri, male; J — Dolgoma cribrata; K — Manulea atratula, female; L — Arctia lapponica lemniscata, male; M, N, O — Saturnia pavonia, larvae, third (M, N) and fifth instars (O), Niman Cordon. A, C, E, G–L — upperside; B, D, F — underside. Scale bar 5 mm in New species of moths (Lepidoptera, Macroheterocera) in the fauna of the Bureinsky Nature Reserve (Russia, Khabarovsky Region)
Рис. 1. Некоторые виΑы Macroheterocera из Буреинского заповеΑника: A, B — Paranthrene tabaniformis, самец; C, D — Synanthedon culiciformis, самец; E, F — S. culiciformis, самец; G — Nordstromia grisearia, самка; H — Cilix filipjevi, самец; I — Macrobrochis staudingeri, самец; J — Dolgoma cribrata; K — Manulea atratula, самка; L — Arctia lapponica lemniscata; M, N, O — Saturnia pavonia, гусеницы третьего (M, N) и пятого возрастов (O), корΑон «Ниман». A, C, E, G–L — верхняя сторона крыΛьев; B, D, F — нижняя. Масштабная Λинейка 5 мм Fig. 1. Some Macroheterocera species from the Bureinsky Nature Reserve:A, B —Paranthrene tabaniformis, male; C, D — Synanthedon culiciformis, male; E, F — S. culiciformis, male; G — Nordstromia grisearia, female; H — Cilix filipjevi, male; I — Macrobrochis staudingeri, male; J — Dolgoma cribrata; K — Manulea atratula, female; L — Arctia lapponica lemniscata, male; M, N, O — Saturnia pavonia, larvae, third (M, N) and fifth instars (O), Niman Cordon. A, C, E, G–L — upperside; B, D, F — underside. Scale bar 5 mm
Fig. 3. Abdominal tergites VIII and IX in A key to some Frankliniella (Thysanoptera: Thripidae) larvae found in Florida with descriptions of the first instar of select species
Fig. 3. Abdominal tergites VIII and IX of larvae II: dorsal setae, D1, D2 of tergites VIII and IX F. bispinosa (A); F. cephalica (B); F. insularis (C); F. kelliae (D); F. occidentalis (E); F. schultzei (F); F. fusca (G); scale = 25 µm.
Fig. 2. Larva II in A key to some Frankliniella (Thysanoptera: Thripidae) larvae found in Florida with descriptions of the first instar of select species
Fig. 2. Larva II of F. bispinosa: dorsal setae pairs, D1–D4 of head (A); dorsal setae pairs, D1–D7 of pronotum (B); dorsal setae pairs, D1–D8 of mesonotum (C); scale = 25 µm.
Fig. 1. Larva I in A key to some Frankliniella (Thysanoptera: Thripidae) larvae found in Florida with descriptions of the first instar of select species
Fig. 1. Larva I of F. kelliae: dorsal setae pairs, D1–D6 of pronotum and D1–D5 of mesonotum (A); arrow indicates small sclerotized teeth between D1 setae of abdominal tergite IX (B); scale = 25 µm.
Fig. 2 in Monitoring the establishment and flight phenology of parasitoids of emerald ash borer (Coleoptera: Buprestidae) in Michigan by using sentinel eggs and larvae
Fig. 2. Percentage of parasitism by Tetrastichus planipennisi of emerald ash borer larvae in larval sentinel logs (pooled by sample date, i.e., the date that larval sentinel logs were collected) in Nancy Moore and Burchfield Parks, Michigan, in (A) 2011, (C) 2012, and (E) 2013, and by Atanycolus spp. in (B) 2011, (D) 2012, and (F) 2013. The secondary Y-axis is growing degree day base 10 °C (GDD10) using the Baskerville–Emin method.
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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.