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73 results for “Dorippidae”
FIG. 34 in Crabs of the subfamily Ethusinae Guinot, 1977 (Crustacea, Decapoda, Brachyura, Dorippidae) of the Indo-West Pacific region
FIG. 34. — Bathymetric distribution of Indo-West Pacific ethusine crabs.
FIG. 17 in Crabs of the subfamily Ethusinae Guinot, 1977 (Crustacea, Decapoda, Brachyura, Dorippidae) of the Indo-West Pacific region
FIG. 17. — Geographical distribution of Ethusina challengeri (Miers, 1886).
FIG. 11 in Crabs of the subfamily Ethusinae Guinot, 1977 (Crustacea, Decapoda, Brachyura, Dorippidae) of the Indo-West Pacific region
FIG. 11. — Geographical distribution of Ethusa hirsuta McArdle, 1900.
FIG. 16 in Crabs of the subfamily Ethusinae Guinot, 1977 (Crustacea, Decapoda, Brachyura, Dorippidae) of the Indo-West Pacific region
FIG. 16. — Ethusina challengeri (Miers, 1886), cl 12.6 mm, cw 12.1 mm, Mozambique Basin, SAFARI 1, stn 1, trawl CP 01, 2608 m (MNHN-B 8775); A, dorsal surface of carapace; B, ventral view of anterior portion of body; C, right G1, ventral (left) and dorsal (right) views; D, left G2, dorsal view. Scale bars: A, 5 mm; B, D, 2 mm; C, 1 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.
FIG. 12 in Crabs of the subfamily Ethusinae Guinot, 1977 (Crustacea, Decapoda, Brachyura, Dorippidae) of the Indo-West Pacific region
FIG. 12. — Geographical distribution of Ethusa indica Alcock, 1894.
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