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343 results for “reproductive system”
Figure 4. Reproductive system. A – D in Dina serbica, a new species of leeches (Annelida: Hirudinea: Erpobdellidae) from Serbia, based on morphological and molecular evidence
Figure 4. Reproductive system. A – D. minuoculata Grosser, Moritz & Pešić, 2007, paratype, a first order stream in the Tara river canyon, Montenegro. B – Dina serbica sp. nov., paratype, spring along the road to Kamena Gora, Serbia. Abbreviations: a = genital atrium, b = vas deferens, c = ovarian sacks, d = testisacs.
Fig. 12. Female reproductive system, ventral view. A in Taxonomic revision of the species of Stenothemus from Southwest China (Coleoptera, Cantharidae), with the descriptions of five new species
Fig. 12. Female reproductive system, ventral view. A. Stenothemus singularicollis (Pic, 1933) comb. nov. (MHBU, Shaanxi). B. S. gracilis Y. Yang & X. Yang sp. nov., paratype (IZAS IOZ(E) 225787). C. S. flavicollis Y. Yang & S. Ge sp. nov., paratype (MHBU HBU(E) 410039). D. S. laticornis Y. Yang & H. Liu sp. nov., paratype (MHBU HBU(E) 410047). Abbreviations: see Material and methods. Scale bars = 0.5 mm.
Figure 1 in Structure of the reproductive system and hectocotylus in males of lesser flying squid Todaropsis eblanae (Cephalopoda: Ommastrephidae)
Figure 1. The range of Todaropsis eblanae and the sampling locations.
Figs. 30–39 in Comparative Study of Mexican Geotrupini (Coleoptera: Scarabaeoidea: Geotrupidae) Reproductive Systems, with Taxonomic Commentaries
Figs. 30–39. Spermathecae of Geotrupini species.
Figures 13–17 in Comparative morphological study of reproductive system between Tipulidae and Limoniidae (Diptera: Tipuloidea)
Figures 13–17. Hexatoma (Eriocera) cleopatroides. 13. Ovipositor and female internal reproductive system, lateral view. 14. Cercus and vaginal apodeme, dorsal view. 15. Hypovalva, dorsal view. 16. Female internal reproductive system, dorsal view. 17. Egg.
Figures 1–5 in Comparative morphological study of reproductive system between Tipulidae and Limoniidae (Diptera: Tipuloidea)
Figures 1–5. Libnotes (Libnotes) pseudonohirai. 1. Hypopygium, dorsal view. 2. Hypopygium, ventral view. 3. Hypopygium, lateral view. 4. Aedeagus and paramere, lateral view. 5. Male internal reproductive system, dorsal view.
Figures 1–8 in A new species of genus Brithura Edwards from China, with notes on its internal reproductive system (Diptera: Tipulidae)
Figures 1–8. Brithura triprocessa Men & Liu sp. nov. 1. Head, dorsal view. 2. Thorax, dorsal view. 3. Thorax, lateral view. 4. Wing. 5. Abdomen, lateral view. 6. Hypopygium, lateral view. 7. Abdomen, lateral view. 8. Ovipositor, lateral view.
Figure 44. Paradoris indecora, reproductive system. A in A taxonomic revision of Paradoris sea slugs (Mollusca, Gastropoda, Nudibranchia, Doridina)
Figure 44. Paradoris indecora, reproductive system. A, remaining pieces, MNHN-Sagres, scale = 3 mm. B, distal part, with a hypothetical stylet sac, MNCN, scale = 0.6 mm. C, general view, ZMUC #1, scale = 0.6 mm. D, remaining pieces, MNHN-Ceuta, scale = 4.3 mm.
Figure 4. Paradoris araneosa, reproductive system. A in A taxonomic revision of Paradoris sea slugs (Mollusca, Gastropoda, Nudibranchia, Doridina)
Figure 4. Paradoris araneosa, reproductive system. A, two accessory glands and one stylet sac in the distal part (the second stylet sac not visible on this side), paratype, CASIZ 121099, scale = 0.9 mm. B, same as (A), on the other side, scale = 0.9 mm. C, spermatic pouches and ducts, paratype, CASIZ 121099, scale = 1.2 mm. D, one accessory gland and two stylet sacs in the distal part, paratype, MNHN-SMIB 8, after Valdés (2001: fig. 33C), scale = 2.1 mm. E, remaining pieces of possibly two accessory glands in the distal part (stylet sacs missing), paratype, MNHN-SMIB 8, scale = 0.8 mm. F, remaining genital pieces, paratype, MNHN-SMIB 8, scale = 2.3 mm. G, general view, paratype, CASIZ 121099, scale = 1.6 mm.
FIG. 36 in A new subfamily classification of the highly diversified Dorippidae H. Milne Edwards, 1837 (Crustacea, Decapoda, Brachyura, Dorippoidea), using morphological, molecular and palaeotonlogical data, with special emphasis on its unique female reproductive system
FIG. 36. — Schematic reconstructions of some female reproductive systems in Brachyura: A, in a podotreme crab, with spermatheca as cuticular invagination derived from a split between plates of intersegmental phragma 7/8, independent of the rest of reproductive system (gonopore on P3 coxa), and with external fertilisation; B, in Dorippe sinica (Dorippinae n. stat.), with glandular and cuticle chambers independent of seminal receptacle (not connected to ovary) and extension of vulva where fertilisation can take place (from Hayer et al. 2016a: fig. 8A). In Paradorippinae n. subfam. (not shown, but see Fig. 35D), without seminal receptacle, the fertilisation occurs externally in vulva opening (according to Vehof et al. 2018b: fig. 3; Vehof 2020); C, in Ethusa mascarone (Ethusidae), with glandular and cuticle chambers largely independent of the seminal receptacle (according to Hayer et al. 2016b: fig. 8); D, in a generalised eubrachyuran (one of several patterns), with seminal receptacle directly connected to ovary via oviduct, with vulvar opening on sternite 6 and with internal fertilisation. Abbreviations: as, spermathecal aperture; cc, cuticule chamber; cx3, coxa of P3 with coxal gonopore; gc, glandular chamber; m, musculature; od, oviduct; ov, ovary; P3, third pereiopod; sp, spermatheca; sr, seminal receptacle; vg, vagina; v, vulva.
FIG. 24. — Paradorippinae n in A new subfamily classification of the highly diversified Dorippidae H. Milne Edwards, 1837 (Crustacea, Decapoda, Brachyura, Dorippoidea), using morphological, molecular and palaeotonlogical data, with special emphasis on its unique female reproductive system
FIG. 24. — Paradorippinae n. subfam. Paradorippe granulata (De Haan, 1841): habitus: A, ♂ 23.6 × 27.3 mm, NE Taiwan, I-Lan county, ZRC 2001.0014; B, ovigerous ♀ 23. 2 × 25.7 mm, Japan, off Hota, ZRC 1999.0082.
FIG. 26. — Paradorippinae n in A new subfamily classification of the highly diversified Dorippidae H. Milne Edwards, 1837 (Crustacea, Decapoda, Brachyura, Dorippoidea), using morphological, molecular and palaeotonlogical data, with special emphasis on its unique female reproductive system
FIG. 26. — Paradorippinae n. subfam. Paradorippe granulata (De Haan, 1841): A-C, ovigerous ♀ 23.2 × 25.7 mm, Japan, off Hota, ZRC 1999.0082. D, ♀ 22.7 × 24, 7 mm, China, Tuandao, off Quingdao, MNHN-IU-2016-10753. A, anterior ventral view; B, C, thoracic sternum and pleon; D, vulvae.
FIG. 22. — Medorippinae n in A new subfamily classification of the highly diversified Dorippidae H. Milne Edwards, 1837 (Crustacea, Decapoda, Brachyura, Dorippoidea), using morphological, molecular and palaeotonlogical data, with special emphasis on its unique female reproductive system
FIG. 22. — Medorippinae n. subfam. Medorippe lanata (Linnaeus, 1767): A, ♂ 18.5 × 23.2 mm, Dahomey Coasts, ZRC 2009.0411: habitus; B, ovigerous ♀ 21.2 × 27.7 mm, Israel, ZRC 1999.0632: habitus; C-E, ♂ 18.5 × 23.2 mm, same data as A: C, anterior ventral view; D, thoracic sternum, press-button and G1; E, G1 and G2. F, ♂ 23.2 × 28.9 mm, no data, ZRC 2009.0412 (ex MNHN): thoracic sternum with pleon.
FIG. 17. — Dorippoidinae n in A new subfamily classification of the highly diversified Dorippidae H. Milne Edwards, 1837 (Crustacea, Decapoda, Brachyura, Dorippoidea), using morphological, molecular and palaeotonlogical data, with special emphasis on its unique female reproductive system
FIG. 17. — Dorippoidinae n. subfam. Dorippoides facchino (Herbst, 1785): A-C, ♂ 25.3 × 32 mm, Malaysia, Johore, Pontian, ZRC 1991.66-72: A, anterior ventral view; B, thoracic sternum with pleon; C, without pleon. D, ovigerous ♀ 21 × 25 mm, South China Sea, MNHN-IU-2018-5195 (= MNHN-B18802): vulvae.
FIG. 15. — Dorippinae H. Milne Edwards, 1837 n in A new subfamily classification of the highly diversified Dorippidae H. Milne Edwards, 1837 (Crustacea, Decapoda, Brachyura, Dorippoidea), using morphological, molecular and palaeotonlogical data, with special emphasis on its unique female reproductive system
FIG. 15. — Dorippinae H. Milne Edwards, 1837 n. stat.: A-D, J, Dorippe trilobata Manning, 1993, holotype, ♂ 20.5 × 21.1 mm, off Mitchell River, Admiralty Gulf, AM P27124: A, habitus; B, ventral surface; C, carapace; D, pleon; J, callosity. E-I: Dorippe glabra Manning, 1993, holotype, ovigerous ♀ 24.3 × 26.7 mm, Chambers Bay, Australia, AM P13363: E, habitus with detached right cheliped, right P2 and P3, left P3; F, carapace; G, ventral surface; H, pleon; I, callosity.
FIG. 38 in A new subfamily classification of the highly diversified Dorippidae H. Milne Edwards, 1837 (Crustacea, Decapoda, Brachyura, Dorippoidea), using morphological, molecular and palaeotonlogical data, with special emphasis on its unique female reproductive system
FIG. 38. — Phylogenetic tree of the concatenated dataset obtained by Bayesian Inference analysis. Numbers above branches indicate Bayesian posterior probabilities; numbers under branches indicate Maximum Likelihood bootstrap values (tree by Valentin de Mazancourt).
FIG. 3 in A new subfamily classification of the highly diversified Dorippidae H. Milne Edwards, 1837 (Crustacea, Decapoda, Brachyura, Dorippoidea), using morphological, molecular and palaeotonlogical data, with special emphasis on its unique female reproductive system
FIG. 3. — Carapace diversity in the nine dorippid genera: A, Dorippe Weber, 1795 (D. quadridens); B, Dorippoides Serène & Romimohtarto, 1969 (D. facchino); C, Medorippe Manning & Holthuis, 1981 (?M. crosnieri); D, Heikeopsis Ng, Guinot & Davie, 2008 (H. aff. japonica); E, Neodorippe Serène & Romimohtarto, 1969 (N. callida); F, Nobilum Serène & Romimohtarto, 1969 (N. histrio); G, Paradorippe Serène & Romimohtarto, 1969 (P. cathayana); H, Philippidorippe Chen, 1986 (P. philippinensis); I, Phyllodorippe Manning & Holthuis, 1981 (P. armata). A-G, I: modified from Sin et al. (2009: fig. 3); H, from Chen (1986: pl. 1, fig. 3). The strip, which is shown here only in Dorippoides facchino (Herbst, 1785) and Medorippe?crosnieri Chen, 1988, is in fact present in all species of dorippids.
Counts of two sperm types during migration in female Manduca sexta reproductive system after mating
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Data from: Precopulatory but not postcopulatory male reproductive traits diverge in response to mating system manipulation in Drosophila melanogaster
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Reproductive systems and low outbreeding barriers between Jacaranda cuspidifolia and J. mimosifolia (Jacarandeae, Bignoniaceae)
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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