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17 results for “Rhynchocinetidae”
FIGURE 6 in Cinetorhynchus gabonensis, a new species of hinge-beak shrimp (Crustacea: Decapoda: Rhynchocinetidae) from the eastern Atlantic
FIGURE 6. Colour pattern in life of three Atlantic species of the genus Cinetorhynchus. A–B, C. gabonensis sp. n., oviger- ous female allotype. C, C. rigens (Gordon, 1936), UO-Mdr.2018.06.08, Madeira. D, C. manningi Okuno, 1996, Brazil. Photos: A, Thomas Menut; B, C, Peter Wirtz; D, Carlos Eduardo Ferreira.
FIGURE 5 in Cinetorhynchus gabonensis, a new species of hinge-beak shrimp (Crustacea: Decapoda: Rhynchocinetidae) from the eastern Atlantic
FIGURE 5. Cinetorhynchus gabonensis sp. n., holotype male. A, fifth to eight thoracic sterna and bases on pereiopods 2–5. B, posterior end on sixth pleomere, and proximal parts of uropods, ventral view. C, first male pleopod, anterior aspect. D, second male pleopod, posterior aspect. E, same, appendices interna and masculina.
FIGURE 3 in Cinetorhynchus gabonensis, a new species of hinge-beak shrimp (Crustacea: Decapoda: Rhynchocinetidae) from the eastern Atlantic
FIGURE 3. Cinetorhynchus gabonensis sp. n., holotype male, mouthparts (right side dissected). A, paragnaths, posteroventral view. B, mandible. C, same, incisor and molar processes, outer view. D, same, with palp, inner view. E, maxillula. F, maxilla. G, first maxilliped. H, second maxilliped. I, third maxilliped. A, unscaled.
FIGURE 4 in Cinetorhynchus gabonensis, a new species of hinge-beak shrimp (Crustacea: Decapoda: Rhynchocinetidae) from the eastern Atlantic
FIGURE 4. Cinetorhynchus gabonensis sp. n., holotype male. A, left first pereiopod, lateral view. B, same, chela and distal carpus. C, left second pereiopod, lateral view. D, same, chela and distal carpus. E, third pereiopod, lateral. F, same, dactylus and distal propodus. G, fourth pereiopod. H, fifth pereiopod.
FIGURE 2 in Cinetorhynchus gabonensis, a new species of hinge-beak shrimp (Crustacea: Decapoda: Rhynchocinetidae) from the eastern Atlantic
FIGURE 2. Cinetorhynchus gabonensis sp. n., holotype male. A, anterior carapace and rostrum, lateral view. B, anterior cephalothorax with left eye and appendages, dorsal. C, part of dorsal margin of rostrum with tegumental scales, lateral. D, detail of tegumental scales laterally on carapace. E, tegumental scale. F, left antennule, lateral. G, left antenna, ventral. H, sixth pleomere, telson, and left uropod, dorsal. I, distal end of telson, dorsal.
FIGURE 7 in Cinetorhynchus gabonensis, a new species of hinge-beak shrimp (Crustacea: Decapoda: Rhynchocinetidae) from the eastern Atlantic
FIGURE 7. Phylogenetic position of Cinetorhynchus gabonensis sp. n. among Atlantic congeners resolved by Maximum Likelihood (ML) method based on the combined 16S and COI gene sequences (with a stenopodid species as outgroup). Maximum Likelihood bootstrap support and Bayesian posterior probabilities (ML/BI) expressed as percentages are indicated in nodes.
FIGURE 1 in Cinetorhynchus gabonensis, a new species of hinge-beak shrimp (Crustacea: Decapoda: Rhynchocinetidae) from the eastern Atlantic
FIGURE 1. Cinetorhynchus gabonensis sp. n., holotype male, habitus, lateral view.
Figure 9 from: Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 187-209. https://doi.org/10.3897/zookeys.457.6512
Figure 9 - Fecundity in Cinetorhynchus species A and B. The log10 number of embryos per brood are plotted against log10 female size (carapace length, mm).
Figure 2 from: Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 187-209. https://doi.org/10.3897/zookeys.457.6512
Figure 2 - Photographs of living Cinetorhynchus species from Coconut Island, Hawaii. A Cinetorhynchus sp. B male with subchelate first chelipeds (pereopod 1) B Cinetorhynchus sp. B male with cheliped intermediate between chelate and subchelate C Cinetorhynchus sp. A male with subchelate chelipeds D Cinetorhynchus sp. B female E Cinetorhynchus sp. A female. C1 cheliped 1; C2 cheliped 2; M3 third maxilliped. Scale bars represent 10 mm.
Figure 8 from: Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 187-209. https://doi.org/10.3897/zookeys.457.6512
Figure 8 - Puncture wounds (unmarked arrows) on the propodi of the major chelipeds of three large Cinetorhynchus males. A Cinetorhynchus sp. A B and C Cinetorhynchus sp. B D Regenerating major cheliped of a male Cinetorhynchus sp. B; only two articles plus a rudimentary cheliped with underdeveloped propodus and dactyl have formed. d dactyl (movable finger); p propodus. Scale bars represent 3 mm.
Figure 5 from: Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 187-209. https://doi.org/10.3897/zookeys.457.6512
Figure 5 - Comparison of third maxillipeds in male and female Cinetorhynchus species. A Maxilliped 3 size (measured as length of terminal article) plotted against body size (carapace length, CL) B Number of corneous spines on the terminal article of maxilliped 3 plotted against body size (CL). In B number of observations is the same as A, except for Cinetorhynchus sp. B males (n=45) and Cinetorhynchus sp. B females (n=13) because spinous portions of the terminal article of some individuals were damaged.
Figure 7 from: Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 187-209. https://doi.org/10.3897/zookeys.457.6512
Figure 7 - Variation in the major chela and chela finger shape with increasing size in males of Cinetorhynchus species B. A female 11.3 mm CL B male 9.4 mm CL C male 10.1 mm CL D male 10.6 mm CL E male 11.4 mm CL. cs corneous (black) seta(e); d dactyl (movable finger); p propodus; pf propodal finger. Unlabeled arrows in D and E show lack of the black corneous setae seen in A–C. Scale bars represent 10 mm.
Figure 6 from: Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 187-209. https://doi.org/10.3897/zookeys.457.6512
Figure 6 - Ontogeny of major chela (pereopod 1) structure from a typical chela to a subchela in Cinetorhynchus species A and B. The length of the propodal finger relative to propodal length (cheliped size) is plotted as the measure of chela structure. With growth, the relative propodal (fixed) finger length decreases in larger males but not in females as male first chelipeds change from chelate to subchelate (see Figure 7). A Cinetorhynchus sp. A B Cinetorhynchus sp. B.
Figure 4 from: Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 187-209. https://doi.org/10.3897/zookeys.457.6512
Figure 4 - Variation of cheliped size in Cinetorhynchus species. Cheliped size (measured as propodal length) is plotted against body size (CL) in male and females. A Cinetorhynchus sp. A B Cinetorhynchus sp. B.
Figure 3 from: Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 187-209. https://doi.org/10.3897/zookeys.457.6512
Figure 3 - Sexual dimorphism in Cinetorhynchus sp. B. A Large male (10.8 mm CL) B Female (8.9 mm CL). Scale bars in A and B represent 10 mm C Distal end of chela 1 of a female (11.2 mm CL) showing blackened corneous setae on chela fingers; scale bar represents 0.5 mm D Illustration of tip of chela 1, Rhynchocinetes albatrossae (from Chace 1997, no scale given), showing form of blackened corneous setae (similar to those shown in Figure 3C) typical of chelipeds 1 and 2 of rhynchocinetids except in large males (e.g., as in this study). C1 cheliped 1; cs corneous setae; dactyl (movable finger); M3 third maxilliped; p propodus; pf propodal (fixed) finger.
Figure 10 from: Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 187-209. https://doi.org/10.3897/zookeys.457.6512
Figure 10 - Variation in female breeding dress characters with increasing size in females in Cinetorhynchus sp. A and Cinetorhynchus sp. B. compared with the same structures in males. A Height of the second abdominal pleuron B Width of the basipod flange of the second pleopod.
Figure 1 from: Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 187-209. https://doi.org/10.3897/zookeys.457.6512
Figure 1 - Size frequency diagrams of male and female Cinetorhynchus species. A Cinetorhynchus sp. A B Cinetorhynchus sp. B.
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