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Figure 2 in Larval development of the spider crab Menaethius monoceros (Latreille, 1825), (Crustacea: Decapoda: Brachyura: Epialtidae)
Figure 2. Second zoea of Menaethius monoceros (Latreille, 1825). (A) lateral view and magnified ventrolateral carapace margin (maxilliped natatory setae shown truncated); (B) antennule; (C) antenna; (D) right mandible; (E) maxillule, with enlargement of coxal and basial endites; (F) maxilla, with enlargement of coxal and basial endites; (G) chela and pereopods; (H) dorsal view of abdomen and telson. Scale bars = 0.1 mm.
Figure 16 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 16. Boasaxius princeps, megalopa. (A) First maxilliped; (B) second maxilliped; (C) third maxilliped; (D) pereiopod 1, left; (E) pereiopod 1, right; (F) pereiopod 2; (G) pereiopod 3; (H) pereiopod 4; (I) pereiopod 5; (J) pleopod; (K) telson with uropods, dorsal view.
Figure 9 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 9. Boasaxius princeps, sixth zoea. (A) Complete larva, dorsal view; (B) same, lateral view; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla.
Figure 12 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 12. Boasaxius princeps, seventh zoea. (A) First maxilliped; (B) second maxilliped; (C) third maxilliped; (D) pereiopod 1; (E) pereiopod 2; (F) pereiopod 3; (G) pereiopod 4; (H) pereiopod 5; (I) telson with uropods, dorsal view.
Figure 6 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 6. Boasaxius princeps, fourth zoea. (A) First maxilliped; (B) second maxilliped; (C) third maxilliped; (D) pereiopod 1; (E) pereiopod 2; (F) pereiopod 3; (G) pereiopod 4; (H) pereiopod 5; (I) telson, with uropods, ventral view.
Figure 5 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 5. Boasaxius princeps, fourth zoea. (A) Complete larva, dorsal view; (B) same, lateral view; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla.
Figure 11 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 11. Boasaxius princeps, seventh zoea. (A) Complete larva, dorsal view; (B) same, lateral view; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla.
Figure 4 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 4. Boasaxius princeps, third zoea. (A) First maxilliped; (B) second maxilliped; (C) third maxilliped; (D) pereiopod 1; (E) pereiopod 2; (F) pereiopod 3; (G) pereiopod 4; (H) pereiopod 5; (I) telson with uropods, ventral view.
Figure 10 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 10. Boasaxius princeps, sixth zoea. (A) First maxilliped; (B) second maxilliped; (C) third maxilliped; (D) pereiopod 1; (E) pereiopod 2; (F) pereiopod 3; (G) pereiopod 4; (H) pereiopod 5; (I) telson with uropods, dorsal view.
Figure 8 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 8. Boasaxius princeps, fifth zoea. (A) Pereiopod 1; (B) pereiopod 2; (C) pereiopod 3; (D) pereiopod 4; (E) pereiopod 5; (F) telson with uropods, dorsal view; (G) same, ventral view.
Figure 14 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 14. Boasaxius princeps, eighth zoea. (A) First maxilliped; (B) second maxilliped; (C) third maxilliped; (D) pereiopod 1; (E) pereiopod 2; (F) pereiopod 3; (G) pereiopod 4; (H) pereiopod 5; (I) pleopod; (J) telson with uropods, ventral view; (K) telson, dorsal view.
Figure 15 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 15. Boasaxius princeps, megalopa. (A) Complete larva, dorsal view; (A′) rostrum, dorsal view; (B) same, lateral view; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla.
Figure 3 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 3. Boasaxius princeps, third zoea. (A) Complete larva, dorsal view; (B) same, lateral view; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla.
Figure 13 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 13. Boasaxius princeps, eighth zoea. (A) Complete larva, lateral view; (B) carapace, dorsral view; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla.
Figure 2 in The complete larval development of the lobster shrimp Boasaxius princeps Boas, 1880 (Decapoda: Axiidea: Axiidae) obtained in the laboratory
Figure 2. Boasaxius princeps, second zoea. (A) Complete larva, dorsal view; (A′) rostral spine; (B) complete larva, lateral view; (B′) anteroventral carapace margin; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla; (H) first maxilliped; (I) second maxilliped; (J) third maxilliped; (K) pereiopods 1 and 2; (L) telson, dorsal view.
Data from: Density-dependent sex-biased development of macroptery in a water strider
<p>In wing-polymorphic insects, wing morphs differ not only in dispersal capability but also in life history traits because of trade-offs between flight capability and reproduction. When the fitness benefits and costs of producing wings differ between males and females, sex-specific trade-offs can result in sex differences in the frequency of long-winged individuals. Furthermore, the social environment during development affects sex differences in wing development, but few empirical tests of this phenomenon have been performed to date. Here, I used the wing-dimorphic water strider <i>Tenagogerris euphrosyne</i> to test how rearing density and sex ratio affect the sex-specific development of long-winged dispersing morphs (i.e., sex-specific macroptery). I also used a full-sib, split-family breeding design to assess genetic effects on density-dependent, sex-specific macroptery. I reared water strider nymphs at either high or low densities and measured their wing development. I found that long-winged morphs developed more frequently in males than in females when individuals were reared in a high-density environment. However, the frequency of long-winged morphs was not biased according to sex when individuals were reared in a low-density environment. In addition, full-sib males and females showed similar macroptery incidence rates at low nymphal density, whereas the macroptery incidence rates differed between full-sib males and females at high nymphal density. Thus complex gene-by-environment-by-sex interactions may explain the density-specific levels of sex bias in macroptery, although this interpretation should be treated with some caution. Overall, my study provides empirical evidence for density-specific, sex-biased wing development. My findings suggest that social factors as well as abiotic factors can be important in determining sex-biased wing development in insects.</p>
Figure 5. Upogebia yokoyai Makarov, 1938 in The larval development of the mud shrimp Upogebia yokoyai Makarov, 1938 (Decapoda: Gebiidea: Upogebiidae) reared under laboratory conditions
Figure 5. Upogebia yokoyai Makarov, 1938, megalopa. (A) Complete larva, dorsal view; (A̓) rostrum, dorsal view; (B) complete larva, lateral view; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla; (H) maxilliped 1; (I) maxilliped 2; (J) maxilliped 3.
Figure 6. Upogebia yokoyai Makarov, 1938 in The larval development of the mud shrimp Upogebia yokoyai Makarov, 1938 (Decapoda: Gebiidea: Upogebiidae) reared under laboratory conditions
Figure 6. Upogebia yokoyai Makarov, 1938, megalopa. (A–E) Pereiopods 1–5; (F) dactylus of pereiopod 5; (G) pleopod 3; (H) uropod; (I) telson, dorsal view.
Figure 3. Upogebia yokoyai Makarov, 1938 in The larval development of the mud shrimp Upogebia yokoyai Makarov, 1938 (Decapoda: Gebiidea: Upogebiidae) reared under laboratory conditions
Figure 3. Upogebia yokoyai Makarov, 1938, third zoea. (A) Complete larva, dorsal view; (B) same, lateral view; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla; (H) first maxilliped; (I) second maxilliped; (J) third maxilliped; (K–O), pereiopods 1–5; (P) telson with uropods, ventral view; (Q) details of telson.
Figure 4. Upogebia yokoyai Makarov, 1938 in The larval development of the mud shrimp Upogebia yokoyai Makarov, 1938 (Decapoda: Gebiidea: Upogebiidae) reared under laboratory conditions
Figure 4. Upogebia yokoyai Makarov, 1938, fourth zoea. (A) Complete larva, dorsal view; (B) same, lateral view; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla; (H) first maxilliped; (I) second maxilliped; (J) third maxilliped; (K–O), pereiopods 1–5; (P) telson with uropods, ventral view.
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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.