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369 results for “Hydroporinae”
FIGURES 17–18 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 17–18. Paroster darlotensis, metathoracic leg (third-instar larva): (17) anterior aspect; (18) posterior aspect. Scale bar = 0.50 mm.
FIGURES 21–22 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 21–22. Paroster macrosturtensis (third-instar larva): (21) head capsule, dorsal aspect (not all secondary setae represented); (22) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bars = 0.20 mm.
FIGURES 5–9 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 5–9. Paroster darlotensis (first-instar larva), head appendages: (5) mandible, dorsal aspect; (6–7) maxilla, (6) dorsal aspect; (7) ventral aspect; (8–9) labium; (8) dorsal aspect; (9) ventral aspect. LA, labium; MN, mandible; MX, maxilla. Numbers and lowercase letters refer to primary setae and pores, respectively. Scale bars = 0.10 mm.
FIGURES 23–24 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 23–24. Paroster mesosturtensis (third-instar larva): (23) head capsule, dorsal aspect (not all secondary setae represented); (24) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bars = 0.20 mm.
FIGURES 1–2 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 1–2. Paroster darlotensis (first-instar larva), head capsule: (1) dorsal aspect; (2) ventral aspect. EB, egg bursters: FR, frontoclypeus; PA, parietale; TP, tentorial pits. Numbers and lowercase letters refer to primary setae and pores, respectively. Scale bar = 0.20 mm.
FIGURES 3–4 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 3–4. Paroster darlotensis (first-instar larva), antenna: (3) ventral aspect; (4) dorsal aspect. AN, antenna. Numbers and lowercase letters refer to primary setae and pores, respectively. Scale bar = 0.10 mm.
FIGURES 43–44 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 43–44. Paroster nigroadumbratus (third-instar larva): (43) head capsule, dorsal aspect (not all secondary setae represented); (44) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 41–42 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 41–42. Paroster niger (third-instar larva): (41) head capsule, dorsal aspect (not all secondary setae represented); (42) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 19–20 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 19–20. Paroster hinzeae (third-instar larva): (19) head capsule, dorsal aspect (not all secondary setae represented); (20) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bars = 0.50 mm.
FIGURES 37–38 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 37–38. Paroster insculptilis (third-instar larva): (37) head capsule, dorsal aspect (not all secondary setae represented); (38) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 31–32 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 31–32. Paroster baylyi (third-instar larva): (31) head capsule, dorsal aspect (not all secondary setae represented); (32) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 35–36 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 35–36. Paroster couragei, metathoracic leg (third-instar larva): (35) anterior aspect; (36) posterior aspect. Scale bar = 0.20 mm.
FIGURES 29–30 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 29–30. Paroster wedgeensis (third-instar larva): (29) head capsule, dorsal aspect (not all secondary setae represented); (30) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bar = 0.20 mm.
FIGURES 12–14 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 12–14. Paroster darlotensis (first-instar larva): (12–13) abdominal segment eight; (12) dorsal aspect; (13) ventral aspect; (14) urogomphus, dorsal aspect; AB, abdominal segment eight; UR, urogomphus. Numbers and lowercase letters refer to primary setae and pores, respectively. Scale bars = 0.10 mm.
FIGURES 10–11 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 10–11. Paroster darlotensis (first-instar larva), metathoracic leg: (10) anterior aspect; (11) posterior aspect. CO, coxa; FE, femur; PT, pretarsus; TA, tarsus; TI, tibia; TR, trochanter. Setae PT1 and PT2 not represented. Numbers and lowercase letters refer to primary setae and pores, respectively. Scale bar = 0.10 mm.
FIGURES 15–16 in Larval morphology of Paroster Sharp, 1882 (Coleoptera: Dytiscidae: Hydroporinae): reinforcement of the hypothesis of monophyletic origin and discussion of phenotypic accommodation to a hypogaeic environment
FIGURES 15–16. Paroster darlotensis (third-instar larva): (15) head capsule, dorsal aspect (not all secondary setae represented); (16) abdominal segment eight and proximal portion of urogomphi, dorsal aspect. Scale bars = 0.50 mm.
Figs. 3–5. Ereboporus naturaconservatus. 3 in North American Stygobiontic Diving Beetles (Coleoptera: Dytiscidae: Hydroporinae) with Description of Ereboporus naturaconservatus Miller, Gibson and Alarie, New Genus and Species, from Texas, U.S.A
Figs. 3–5. Ereboporus naturaconservatus. 3) male genitalia, right lateral aspect; 4) male median lobe, ventral aspect; 5) female genitalia. BC 5 bursa copulatrix, CO 5 common oviduct, FD 5 fertilization duct, GC 5 gonocoxa, GS 5 gonocoxosternite, RE 5 receptacle, SD 5 spermathecal duct, SP 5 spermatheca.
Fig. 17 in North American Stygobiontic Diving Beetles (Coleoptera: Dytiscidae: Hydroporinae) with Description of Ereboporus naturaconservatus Miller, Gibson and Alarie, New Genus and Species, from Texas, U.S.A
Fig. 17. Map of state of Texas, U.S.A. showing extent of several related aquifer systems and known distribution of Comaldessus stygius, Haideoporus texanus and Ereboporus naturaconservatus.
Figs. 6–16. Subterranean Dytiscidae. 6–8 in North American Stygobiontic Diving Beetles (Coleoptera: Dytiscidae: Hydroporinae) with Description of Ereboporus naturaconservatus Miller, Gibson and Alarie, New Genus and Species, from Texas, U.S.A
Figs. 6–16. Subterranean Dytiscidae. 6–8) Comaldessus stygius, 6) dorsal habitus, 7) male genitalia, ventral aspect, 8) male genitalia, right lateral aspect. 9–12) Stygoporus oregonensis, 9) dorsal habitus, 10) male median lobe, right lateral aspect, 11) male median lobe, ventral aspect, 12) male right lateral lobe, right lateral aspect. 13–16) Haideoporus texanus, 13) dorsal habitus, 14) male median lobe, right lateral aspect, 15) male median lobe, ventral aspect, 16) male right lateral lobe, right lateral aspect. Scale bar 5 0.5 mm.
Figs. 2–6. Zimpherus nancae. 2–4 in Zimpherus nancaeMiller and Wheeler (Coleoptera: Dytiscidae: Hydroporinae: Bidessini), New Genus and New Species from Venezuela
Figs. 2–6. Zimpherus nancae. 2–4) Male genitalia: 2) Median lobe, right lateral aspect; 3) Right lateral lobe, right lateral aspect; 4) Median lobe, ventral aspect; 5) Left metatrochanter, anterior aspect. 6) Prosternal process. Scale bars: A = 0.5 mm for Fig. 5; B = 0.2 mm for Fig. 6.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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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.