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272 results for “HARDI”
Brinly-Hardy Co Watch Fob
Brinly Hardy co. Watch Fob circa 1910 (44SD203) Not to Scale Model by Emma Dietrich This model was made using RealityCapture software by Capturing Reality Source: Objaverse 1.0 / Sketchfab
Cold hardiness, deacclimation, and budbreak phenology in grapevine
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Sex linkage of the skeletal muscle sodium channel gene (SCN4A) explains apparent deviations from Hardy–Weinberg equilibrium of tetrodotoxin-resistance alleles in garter snakes (Thamnophis sirtalis)
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FIGURES 10–15 in Endemism within endemism: a new species of Austroleptis Hardy, 1920 (Diptera Austroleptidae) from the Brazilian Atlantic Forest highlands
FIGURES 10–15. Terminalia of Austroleptis camposgerais sp. nov., female, holotype. 10. Abdomen, ventral view with spermathecae. 11. Abdomen, lateral view, position of spermathecae visible. 12. Spermathecae. 13. Terminalia, dorsal view. 14. Terminalia, lateral view. 15. Terminalia, ventral view. Scale bar, 0.1 mm. Abbreviations: cerc, cercus; spmth dt, spermathecal duct; spmth, spermatheca; st, sternite; tg, tergite.
FIGURE 20 in Endemism within endemism: a new species of Austroleptis Hardy, 1920 (Diptera Austroleptidae) from the Brazilian Atlantic Forest highlands
FIGURE 20. Assumed relationship between the three species of Austroleptis, overlapped to the limits of the "Southern Atlantic Forest" area of endemism (Amorim & Santos 2017), based on species of different groups of Diptera.
Data from: Stage-specific genotype-by-environment interactions for cold and heat hardiness in Drosophila melanogaster.
Environments often vary across a life cycle, imposing fluctuating natural selection across development. Such fluctuating selection can drive evolutionary responses specific to distinct life-history stages. However, selection and genetic variation, phenotypic plasticity, and their interaction (GxE), as well as genetic correlation across development dictate stage-specific evolution. Thus, quantifying genetic covariance of fitness-related traits and plasticity across development is vital to determine whether stage-specific adaptation occurs in nature. Additionally, the interaction of genetic variation and environmental plasticity (GxE) may be stage-specific, leading to a 3-way interaction between genotype, environment, and development or GxDxE. To test for these patterns in a natural system, we exposed larvae and adults of Drosophila melanogaster isogenic lines derived from a natural population to extreme heat and cold after developmental acclimation to cool (18°C) and warm (25°C) conditions and measured genetic variance for thermal hardiness. We detected significant GxE that was specific to larvae and adults for cold and heat hardiness (GxDxE), but no significant genetic correlation across development for either trait at either acclimation temperature. However, cross-development phenotypic correlations for acclimation responses suggest that plasticity itself may be developmentally constrained, though rigorously testing this hypothesis requires more experimentation. In general, we find evidence for thermal niche adaptation across development as larvae are more heat-hardy while adults are more cold-hardy. These results illustrate the potential for stage-specific adaptation within a complex life cycle and highlight the importance of measuring traits at appropriate developmental stages and environmental conditions when predicting evolutionary responses to changing climates.
FIGURES 13–18. 13 in Robber flies of South Korea IV. Species of the subfamily Stichopogoninae Hardy, 1930 (Diptera: Asilidae)
FIGURES 13–18. 13. Lasiopogon leleji Ventral genitalia; 14. Lasiopogon leleji Dorsal gonostylus; 15. Lasiopogon rokuroi Ventral genitalia; 16. Lasiopogon rokuroi Dorsal gonostylus; 17. Lasiopogon terneicus Ventral genitalia; 18. Lasiopogon terneicus Dorsal gonostylus
FIGURES 7–12. 7 in Robber flies of South Korea IV. Species of the subfamily Stichopogoninae Hardy, 1930 (Diptera: Asilidae)
FIGURES 7–12. 7. Lasiopogon akaishii Ventral genitalia; 8. Lasiopogon akaishii Dorsal gonostylus; 9. Lasiopogon hasanicus Ventral genitalia; 10. Lasiopogon hasanicus Dorsal gonostylus; 11. Lasiopogon hinei Ventral genitalia; 12. Lasiopogon hinei Dorsal gonostylus
FIGURES 1–6. 1 in Robber flies of South Korea IV. Species of the subfamily Stichopogoninae Hardy, 1930 (Diptera: Asilidae)
FIGURES 1–6. 1. Stichopogon elegantulus orientalis Wing; 2. Lasiopogon rokuroi Wing; 3. Lasiopogon rokuroi Head; 4. Stichopogon elegantulus orientalis Head; 5. Lasiopogon rokuroi Epandria; 6. Stichopogon elegantulus orientalis Epandria.
FIGURES 25–30. 25 in Robber flies of South Korea IV. Species of the subfamily Stichopogoninae Hardy, 1930 (Diptera: Asilidae)
FIGURES 25–30. 25. Stichopogon elegantulus orientalis Gonopod; 26. Stichopogon elegantulus orientalis Aedeagus; 27. Stichopogon inaequalis Gonopod; 28. Stichopogon inaequalis Aedeagus; 29. Stichopogon nartshukae Gonopo; 30. Stichopogon nartshukae Aedeagus.
FIGURES 19–24. 19 in Robber flies of South Korea IV. Species of the subfamily Stichopogoninae Hardy, 1930 (Diptera: Asilidae)
FIGURES 19–24. 19. Stichopogon elegantulus orientalis Male; 20. Stichopogon elegantulus orientalis Female; 21. Stichopogon inaequalis Male; 22. Stichopogon inaequalis Female; 23. Stichopogon nartshukae Male; 24. Stichopogon nartshukae Female.
FIGURES 31–38. Gastrozona parviseta Hardy. 31 in A new species of Gastrozona Bezzi (Diptera: Tephritidae: Dacinae: Gastrozonini) with an updated key to species from India
FIGURES 31–38. Gastrozona parviseta Hardy. 31, head (profile); 32, scutum (dorsal view); 33, thorax (lateral) and legs; 34, abdomen (male); 35, wing; 36, epandrium, proctiger and surstyli (lateral view); 37, epandrium and surstyli (posterior view); 38, glans of phallus (lateral view).
FIGURES 10–14. Ectopomyia baculigera Hardy. 10 in A new species of Magnimyiolia Shiraki (Diptera: Tephritidae: Trypetinae) and new records of Acanthonevrini from India
FIGURES 10–14. Ectopomyia baculigera Hardy. 10, habitus (lateral); 11, head; 12, thorax; 13, abdomen; 14, wing.
Fig. 13 in Polylamina Hardy, A Junior Synonym Of Polyphylla Harris (Coleoptera: Scarabaeidae, Melolonthinae, Melolonthini)
Fig. 13. Shortest tree of relationships among P. variolosa, P. pubescens, P. annamensis, H. mixta and D. caseyi, obtained with exhaustive search algorithm of PAUP (Length 11, CI 5 0.81, RI 5 0.80). Ambiguous character changes optimized using Farris optimization (ACCTRAN).
Fig. 13 in Polylamina Hardy, A Junior Synonym Of Polyphylla Harris (Coleoptera: Scarabaeidae, Melolonthinae, Melolonthini)
Fig. 13. Shortest tree of relationships among P. variolosa, P. pubescens, P. annamensis, H. mixta and D. caseyi, obtained with exhaustive search algorithm of PAUP (Length 11, CI = 0.81, RI = 0.80). Ambiguous character changes optimized using Farris optimization (ACCTRAN).
FIGURES 56–60. Dilophus paucidens Hardy, 1962. 56. Male, wing. 57 in Revision of the genus Dilophus Meigen, 1803 (Diptera, Bibionidae) from the Afrotropical Ecozone
FIGURES 56–60. Dilophus paucidens Hardy, 1962. 56. Male, wing. 57. Male, head and thorax. 58. Male, fore tibia. 59. Male, terminalia, dorsal. 60. Male, terminalia, ventral.
FIGURES 35–40 in First two species of Austroleptis Hardy (Diptera: Brachycera: Austroleptidae) from Brazil
FIGURES 35–40. HAbITuS Of Austroleptis, fEmAlE. 35. A. atriceps, lATERAl VIEW. 36. A. penai, lATERAl VIEW. 37–38. A. longirostris nov. sp., hOlOTYPE, RESPEcTIVElY dORSAl ANd lATERAl VIEWS. 39–40. A. papaveroi nov. sp., lATERAl VIEWS. ScAlE bAR, 1 mm.
FIGURES 26–30 in First two species of Austroleptis Hardy (Diptera: Brachycera: Austroleptidae) from Brazil
FIGURES 26–30. PhOTOgRAPhS Of fEmAlE TERmINAlIA Of Austroleptis (26–29. A. papaveroi nov. sp., PARATYPE) 26. DORSOlATERAl VIEW, INcludINg SPERmAThEcAE. 27. DORSAl VIEW fROm TERgITE 8. 28. LATERAl VIEW fROm TERgITE 8. 29. VENTRAl VIEW fROm STERNITE 8. 30. A. longirostris nov. sp., dORSAl VIEW fROm TERgITE 8, hOlOTYPE. ScAlE bAR, 0.1 mm. AbbREVIATIONS: cERc, cERcuS; ST, STERNITE; Tg, TERgITE.
FIGURES 31–34 in First two species of Austroleptis Hardy (Diptera: Brachycera: Austroleptidae) from Brazil
FIGURES 31–34. FEmAlE TERmINAlIA Of Austroleptis. 31–32. A. longirostris nov. sp., hOlOTYPE, RESPEcTIVElY dORSAl ANd VENTRAl VIEWS. 33–34. A. papaveroi nov. sp., PARATYPE, PARATYPE, RESPEcTIVElY dORSAl ANd VENTRAl VIEWS. AbbREVIATIONS: cERc, cERcuS; gEN fk, gENITAl fORk; ST, STERNITE; Tg, TERgITE.
FIGURES 24–25 in First two species of Austroleptis Hardy (Diptera: Brachycera: Austroleptidae) from Brazil
FIGURES 24–25. FEmAlE REPROducTIVE TRAcTS Of Austroleptis, INcludINg gENITAl fORk. 24. A. longirostris nov. sp., hOlOTYPE. 25. A. papaveroi nov. sp., PARATYPE. ScAlE bAR, 0.1 mm.
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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.