376 V.M. Tuset et al. / Fisheries Re<strong>sea</strong>rch 109 (2011) 373–378 Fig. 4. Phases of egg <strong>development</strong>. (For <strong>in</strong>terpretation of the references to color <strong>in</strong> this figure legend, the reader is refer<strong>red</strong> to the web version of the article.) while <strong>in</strong> C. qu<strong>in</strong>quedens they are <strong>red</strong>-orange, then brown, purple, <strong>and</strong> f<strong>in</strong>ally black (Wigley et al., 1975; Haefner, 1978; Erdman <strong>and</strong> Blake, 1988). Crabs of genus Chaceon <strong>in</strong>habit <strong>deep</strong> waters <strong>and</strong> seem to have cont<strong>in</strong>uous reproduction along year (Elner et al., 1987; Erdman <strong>and</strong> Blake, 1988; Steimle et al., 2001; P<strong>in</strong>ho et al., 2001; Smith et al., 2004). Berried females migrate to shallower <strong>and</strong> warmer waters enhanc<strong>in</strong>g eggs that are swept up surface by the current (Haefner, Table 1 Morphological values (mean ± st<strong>and</strong>ard deviation) of stages of egg <strong>development</strong>. 1978). The larvae phase is pelagic <strong>and</strong> consists <strong>in</strong> four zoeal stages <strong>and</strong> a f<strong>in</strong>al megalopa. In the first postmegalop <strong>in</strong>star stage the carapace width is relatively large, which may be an adaptation to slow post-settlement growth (see Steimle et al., 2001). The eggs are the largest known for crabs with planktonic <strong>development</strong>: 600 m <strong>in</strong> maximum diameter <strong>in</strong> C. fenneri (Erdman <strong>and</strong> Blake, 1988; H<strong>in</strong>es, 1988; Erdman et al., 1991) <strong>and</strong> C. bicolour (Smith et al., 2004), 680 m D <strong>in</strong> C. maritae (Melville-Smith, 1987), 789 m D <strong>in</strong> C. Stage n Maximum diameter (D, mm) M<strong>in</strong>imum diameter (d, mm) Area (A, mm 2 ) Roundness Ratio aspect I 302 0.585 ± 0.031 0.551 ± 0.029 0.254 ± 0.026 1.075 ± 0.007 1.097 ± 0.031 II 2042 0.582 ± 0.039 0.541 ± 0.043 0.251 ± 0.034 1.124 ± 0.081 1.157 ± 0.062 III 616 0.580 ± 0.043 0.551 ± 0.045 0.257 ± 0.038 1.078 ± 0.009 1.115 ± 0.039 IV 326 0.590 ± 0.047 0.558 ± 0.048 0.262 ± 0.042 1.077 ± 0.008 1.126 ± 0.043 V 533 0.601 ± 0.033 0.566 ± 0.035 0.272 ± 0.030 1.081 ± 0.009 1.131 ± 0.050 VI 334 0.655 ± 0.038 0.627 ± 0.036 0.328 ± 0.036 1.083 ± 0.008 1.109 ± 0.040
Fig. 5. Relationships between <strong>fecundity</strong> <strong>and</strong> carapace width (A) <strong>and</strong> total weight (B). aff<strong>in</strong>is (present study), <strong>and</strong> 846 m D <strong>in</strong> C. qu<strong>in</strong>quedens (Haefner, 1978; Elner et al., 1987; H<strong>in</strong>es, 1988; Erdman et al., 1991). However, large egg size has reproductive implications by decreas<strong>in</strong>g the number of eggs (H<strong>in</strong>es, 1982, 1988). Comparison of <strong>fecundity</strong> estimates <strong>in</strong> <strong>deep</strong>-<strong>sea</strong> <strong>red</strong> crabs does not reveal great differences among species, although it can be concluded that there is a positive correlation female size <strong>and</strong> the number of eggs: 36,000–226,000 eggs (90–118 mm CW) <strong>in</strong>C. qu<strong>in</strong>quedens (H<strong>in</strong>es, 1988; Steimle et al., 2001), 15,592–288,312 eggs (98–133 mm CW) <strong>in</strong>C. bicolor (Smith et al., 2004), 107,000–350,000 <strong>in</strong> C. maritae (Melville- Smith, 1987), 160,000–375,000 eggs (110–143 mm CW)<strong>in</strong>C. fenneri (Erdman <strong>and</strong> Blake, 1988; H<strong>in</strong>es, 1988), <strong>and</strong> 199,690–566,956 eggs (105–160 mm CW)<strong>in</strong>C. aff<strong>in</strong>is (present study). In all these species it has been found that <strong>fecundity</strong> <strong>in</strong>creased with the <strong>in</strong>crease of carapace width or wet weight of the <strong>in</strong>dividuals (Melville-Smith, 1987; Erdman <strong>and</strong> Blake, 1988; H<strong>in</strong>es, 1988; Steimle et al., 2001; Smith et al., 2004; present study), as also occurs <strong>in</strong> other brachyurans (Haddon, 1994; Mantelatto <strong>and</strong> Fransozo, 1997; Litulo, 2004, 2005; Arshad et al., 2006). However, <strong>in</strong> <strong>deep</strong>-<strong>sea</strong> <strong>red</strong> crabs it has been noted that these variables are not good p<strong>red</strong>ictors of <strong>fecundity</strong>, reach<strong>in</strong>g variability values of 45–65% (C. qu<strong>in</strong>quedens, C. fenneri, <strong>and</strong> C. aff<strong>in</strong>is) or at least 13–26% (C. bicolor). Also, it is known crabs V.M. Tuset et al. / Fisheries Re<strong>sea</strong>rch 109 (2011) 373–378 377 can lose eggs dur<strong>in</strong>g <strong>in</strong>cubation through di<strong>sea</strong>se, egg p<strong>red</strong>ation, or other k<strong>in</strong>ds of natural failure of egg <strong>development</strong> (Perk<strong>in</strong>s, 1971). The high variability may be due to the large time that females carry the eggs as the <strong>in</strong>cubation period may last up to n<strong>in</strong>e months (Haefner, 1978; Erdman et al., 1991). It can be hypothesized that the use of females with eggs <strong>in</strong> different stages of <strong>development</strong> could <strong>in</strong>fluence the <strong>fecundity</strong> estimates. Nevertheless, Erdman <strong>and</strong> Blake (1988) <strong>and</strong> H<strong>in</strong>es (1988) found a similar trend for Chaceon spp. select<strong>in</strong>g only embryos <strong>in</strong> early stage. Moreover, our results prove that the comparative study between automated system versus manual count<strong>in</strong>g, <strong>and</strong> also between fresh versus fixed samples, were not caus<strong>in</strong>g this high variability. Consequently, this study provides relevant <strong>in</strong>formation for stock assessment of this species, moreover the analysis of the colour of the eggs <strong>and</strong> their <strong>development</strong> may be used for a susta<strong>in</strong>able fish<strong>in</strong>g due to the quick observation. Acknowledgements The authors are <strong>in</strong>debted to José A. Pérez-Peñalvo, Rosa Domínguez-Seoane <strong>and</strong> Eliseba García for skilful technical assistance. F<strong>in</strong>ancial support was received from the EU ERDF <strong>in</strong> the framework of the PIC INTERREG III B project PESCPROF-2 (03/MAC/4.2/M8) <strong>and</strong> from the Spanish Government <strong>in</strong> the framework of project REDECA (CTM2005-07712-C03/MAR). References Arana, P.M., 2000. Estimación de abundancia y biomasa del cangrejo dorado (Chaceon chilensis), en el archipiélago de Juan Fernández, Chile. Inv. Mar. 28, 53–68. Arshad, A., Kamarud<strong>in</strong>, M.S., Saad, C.R., 2006. Study on <strong>fecundity</strong> <strong>and</strong> larval <strong>development</strong> of blue swimm<strong>in</strong>g crab Portunus pelagicus (L<strong>in</strong>naeus, 1758) under laboratory conditions. Res. J. Fish. Hydrobiol. 1, 35–44. Biesiot, P.M., Perry, H.M., 1995. 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