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.
211
datasets available to search
ShareScore release 0.9.0
Dataset results
211 results for “Feeding habits”
FIGURE 30. O in Revision of the genus Odocnemis Allard, 1876 (Coleoptera: Tenebrionidae: Helopini) from Turkey, the Caucasus and Iran with observations on feeding habits
FIGURE 30. O. euritopica sp. n. A) Aedeagus, ventral view. B) Aedeagus, lateral view. C) Inner sternite VIII. D) Gastral spicula. E) Genital tubes (v—vagina, g—gland, s—spermatheca, bd—basal duct of spermatheca). F) Abdominal ventrite 5. G– J) Pronotum. K) Protibia. L) Mesotibia. A–D), G), H), K), L) Male. E), F), I), J) Female. Scale bars— 1mm.
FIGURE 24. O. protina. A in Revision of the genus Odocnemis Allard, 1876 (Coleoptera: Tenebrionidae: Helopini) from Turkey, the Caucasus and Iran with observations on feeding habits
FIGURE 24. O. protina. A) Aedeagus, ventral view. B) Aedeagus, lateral view. C) Inner sternite VIII. D) Gastral spicula. E) Protibia. F) Mesotibia. G) Metatibia. H) Head. I), J) Pronotum. A–I) Male. J) Female. Scale bars—1 mm.
FIGURE 25. O. operta, male. A in Revision of the genus Odocnemis Allard, 1876 (Coleoptera: Tenebrionidae: Helopini) from Turkey, the Caucasus and Iran with observations on feeding habits
FIGURE 25. O. operta, male. A) Head. B) Pronotum. C) Protibia. D) Mesotibia. E) Metatibia. F) Aedeagus, ventral view. G) Aedeagus, lateral view. H) Inner sternite VIII. I) Gastral spicula. J) Protibia. K) Mesotibia. A–E) holotype (pygmy male). F–K) Normal male from Abant Dağı. Scale bars—1 mm.
FIGURE 22. O in Revision of the genus Odocnemis Allard, 1876 (Coleoptera: Tenebrionidae: Helopini) from Turkey, the Caucasus and Iran with observations on feeding habits
FIGURE 22. O. altimontana sp. n. A) Aedeagus, ventral view. B) Aedeagus, lateral view. C) Inner sternite VIII. D) Gastral spicula. E) Protibia. F) Mesotibia. G) Metatibia. H), I) Pronotum. A–H) Male. I) Female. Scale bars—1 mm.
FIGURE 39. O. subtuberculigera thracica subsp. n. and O. gloriosa. A in Revision of the genus Odocnemis Allard, 1876 (Coleoptera: Tenebrionidae: Helopini) from Turkey, the Caucasus and Iran with observations on feeding habits
FIGURE 39. O. subtuberculigera thracica subsp. n. and O. gloriosa. A) Pronotum of O. t. thracica, male. B) The same, female. C) Protibia of O. gloriosa. Scale bars—1mm.
FIGURE 28. O in Revision of the genus Odocnemis Allard, 1876 (Coleoptera: Tenebrionidae: Helopini) from Turkey, the Caucasus and Iran with observations on feeding habits
FIGURE 28. O. aegaeica sp. n. A) Aedeagus, ventral view. B) Aedeagus, lateral view. C) Inner sternite VIII. D) Gastral spicula. E–G) Pronotum. H) Protibia. I) Mesotibia. A–F), H), I) Male. G) Female. Scale bars—1 mm.
FIGURE 27. O. dasypa. A in Revision of the genus Odocnemis Allard, 1876 (Coleoptera: Tenebrionidae: Helopini) from Turkey, the Caucasus and Iran with observations on feeding habits
FIGURE 27. O. dasypa. A) Aedeagus, ventral view. B) Aedeagus, lateral view. C) Inner sternite VIII. D) Gastral spicula. E) Genital tubes (v—vagina, o—oviduct, g—gland, s—spermatheca). F) Protibia. G) Mesotibia. H) Metatibia. I), J) Pronotum. A– D), F–I) Male. E), J) Female. Scale bars—1 mm.
FIGURE 21. O in Revision of the genus Odocnemis Allard, 1876 (Coleoptera: Tenebrionidae: Helopini) from Turkey, the Caucasus and Iran with observations on feeding habits
FIGURE 21. O. shokhini sp. n. A) Aedeagus, ventral view. B) Aedeagus, lateral view. C) Inner sternite VIII. D) Gastral spicula. E) Protibia. F) Mesotibia. G) Metatibia. H–K) Pronotum. A–I) Male. I), K) Female. Scale bars—1 mm.
FIGURE 45. A–D in Revision of the genus Odocnemis Allard, 1876 (Coleoptera: Tenebrionidae: Helopini) from Turkey, the Caucasus and Iran with observations on feeding habits
FIGURE 45. A–D) O. inornata sp. n. E), F) O. shokhini sp. n. G), H) O. altimontana sp. n. A), C), E), G) Males. B), D), F), H) Females.
FIGURES 13–16 13–15 in A new species of the genus Gortyna Ochsenheimer, 1816 from China, with notes on the larval feeding habits (Lepidoptera, Noctuidae, Noctuinae: Apameini)
FIGURES 13–16 13–15. Larva feeding on the host plant and the state of the host after being attacked; 16. Adult living habitus.
FIGURES 1–6 in A new species of the genus Gortyna Ochsenheimer, 1816 from China, with notes on the larval feeding habits (Lepidoptera, Noctuidae, Noctuinae: Apameini)
FIGURES 1–6 Adults of Gortyna spp.. 1. G. guizhouensis sp. n., male, holotype; 2. ditto, female, paratype; 3. ditto, male, paratype; 4. ditto, male, paratype; 5. G. plumbitincta Hreblay & Ronkay, 1997, male (photo by Dr. Shipher Wu); 6. ditto, female, paratype (after Hreblay and Ronkay 1997). Scale bar: 1 cm.
FIGURES 7–12 in A new species of the genus Gortyna Ochsenheimer, 1816 from China, with notes on the larval feeding habits (Lepidoptera, Noctuidae, Noctuinae: Apameini)
FIGURES 7–12 Genitalia of Gortyna spp.. 7. G. guizhouensis sp. n., male, holotype, genit. slide no. hhl-4877-1; 8. ditto, male, paratype, genit. slide no. hhl-4875-1; 9. ditto, male, paratype, genit. slide no. hhl-4874-1; 10. G. plumbitincta Hreblay & Ronkay, 1997, male, genit. slide no. CCMF-SW-NOC-02 (photo by Dr. Shipher Wu); 11. G. guizhouensis sp. n., female, paratype, genit. slide no. hhl-4876-2; 12. G. plumbitincta Hreblay & Ronkay, 1997, female, paratype (after Hreblay and Ronkay 1997). Scale bars: 2 mm.
Data from: Cretaceous lophocoronids with short proboscis and retractable female genitalia provide the earliest evidence for their feeding and oviposition habits
<p>We describe two new species of Lophocoronidae: <em>Acanthocorona hedida</em> Zhang, Shih and Engel <strong>sp. n.</strong> and <em>Acanthocorona venulosa </em>Zhang, Shih and Engel <strong>sp. n.</strong>, and an undetermined specimen from mid-Cretaceous Kachin amber. Phylogenetic analysis of basal lepidopteran lineages, including three extinct families, was undertaken. The analysis supported monophyly of Glossata although internal relationships remain controversial. <em>Acanthocorona </em>and <em>Lophocorona </em>form a monophyletic group. It is likely that short and simply structured proboscides of <em>Acanthocorona </em>were used to sip water droplets, pollination drops from gymnosperms, nectar from early flowers, or sap from injured leaves. Both retracted and extended ovipositors are preserved in the material reported here, revealing their morphology and indicating that these Cretaceous lophocoronids inserted eggs into the tissues of their host plants.</p>
Fig. 1 in Possible Indicators of Feeding Habit Types: Analysis of the Mouthparts of Five Dichotomius Hope (Coleoptera: Scarabaeidae) Species from Argentina
Fig. 1. Mouthparts of the five studied species of Dichotomius: D. carbonarius, D. sericeus, D. nisus, D. mormon, and D. depressicollis. A) Epipharynx and B) Labium (glossa and paraglossa) in dorsal view and hypopharynx. The D. nisus epipharynx shows the presence of a mite basally.
Figure 1 in Feeding habits of the endemic tropical parthenogenetic lizard Cnemidophorus nativo (Teiidae) in a restinga area of northeastern Brazil
Figure 1. Monthly number of isopterans and larvae in relation to total number of consumed prey by Cnemidophorus nativo in the restinga of Guaratiba, Prado, BA, Brazil. Lizard sample sizes for each month are given above the bars.
FIG. 21 in Three new species of the genus Macandrewella (Copepoda: Calanoida: Scolecitrichidae) from the Paci®c Ocean, with notes on distribution and feeding habits
FIG. 21. Distribution of Macandrewella. Note that their distribution is restricted between 30ssN and 20ssS in the Indo-Paci®c. (1) M. chelipes (Campaner, 1989). (2) M. chelipes (Giesbrecht, 1896). (3) M. cochinensis (Gopalakrishnan, 1973). (4) M. scotti and M. chelipes (Sewell, 1929). (5) M. sewelli (Wilson, 1950). (6) M. stygiana and M. omorii (present study). (7) M. joanae (Scott, 1909). (8) M. asymmetrica, M. mera and M. sewelli (Farran, 1936). (9) M. agassizi (Wilson, 1950). (10) M. sewelli (Wilson, 1950). (11) M. serratipes (as M. chelipes, Wilson, 1950; see material examined of M. serratipes).
FIG. 18 in Three new species of the genus Macandrewella (Copepoda: Calanoida: Scolecitrichidae) from the Paci®c Ocean, with notes on distribution and feeding habits
FIG. 18. Gut contents of Macandrewella omorii, n. sp., female. (A) Fragments of radiolarians and crustaceans. (B) Radiolarian fragments. Scales 50.01 mm.
FIG. 15. Macandrewella omorii, n in Three new species of the genus Macandrewella (Copepoda: Calanoida: Scolecitrichidae) from the Paci®c Ocean, with notes on distribution and feeding habits
FIG. 15. Macandrewella omorii, n. sp., male (paratype). (A) Prosomal ends and urosome, dorsal view. (B) Anal somite and caudal rami, ventral view. (C) Antennulary segments I to X±XV. (D) Antennulary segments XVI±XVII to XXII. (E) Antennulary segments XXIII to XXVII±XXVIII. (F) Antennulary compound segment XXVII±XXVIII. (G) Left leg 5. (H) Right leg 5. (I) Terminal portion of left exopod of leg 5. (J) Inner margin of left endopod of leg 5.
FIG. 9 in Three new species of the genus Macandrewella (Copepoda: Calanoida: Scolecitrichidae) from the Paci®c Ocean, with notes on distribution and feeding habits
FIG. 9. SEM micrographs of terminal portion of exopod of left leg 5 of male Macandrewella stygiana, n. sp. Elements indicated by`a' ±`d'. See also ®gure 16. Scales 50.05 mm.
FIG. 8. Macandrewella stygiana, n in Three new species of the genus Macandrewella (Copepoda: Calanoida: Scolecitrichidae) from the Paci®c Ocean, with notes on distribution and feeding habits
FIG. 8. Macandrewella stygiana, n. sp., male (paratypes) (A±J) and M. omorii, n. sp., male (paratype) (K±M). (A) Maxilliped with abnormal endopod. (B) Normal terminal endopodal segments of maxilliped. (C, K) Endopod of leg 2, anterior surface. (D, L) Endopod of leg 3, anterior surface. (E, M) Endopod of leg 4, anterior surface. (F) Left leg 5. (G) Right leg 5. (H, I) Terminal portion of left endopod of leg 5. (J) Terminal portion of left exopod of leg 5.
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.