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Kyne & Simpfendorfer.. - Shark Specialist Group

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Balart et al. (2000) is 295mm TL for females and 298mm TL for males. Both Bythaelurus<br />

clevai and B. lutarius produce small litters of two (one embryo per uterus) (Compagno et al.<br />

2005).<br />

Both single and multiple oviparity can occur amongst the Galeus species, but only single<br />

oviparity is known in Apristurus, Parmaturus and Scyliorhinus (Cross 1988, Ebert et al.<br />

2006). Of the multiple oviparous sawtail sharks, G. melastomus can possess up to 13 egg<br />

cases in the uteri at one time, while G. atlanticus has been observed to carry up to nine egg<br />

cases in the uteri at one time (Muñoz-Chápuli and Perez Ortega 1985, Iglésias et al. 2002).<br />

For the oviparous Bythaelurus, only single oviparity has been observed, while Halaelurus are<br />

multiple oviparous (Compagno et al. 2005, Francis 2006).<br />

For oviparous species, estimates of fecundity are difficult as egg-laying periods and rates are<br />

mostly unknown. Ovarian fecundity may provide a proxy, but as noted previously, the<br />

relationship between the number of follicles and actual reproductive output is not clear.<br />

Castro et al. (1988) determined egg-laying rates in Scyliorhinus retifer held in captivity with<br />

pairs of egg cases laid at intervals of 14.1-16.7 days (average ~15.3 days). Taking this<br />

average and assuming continuous, year-round egg-laying activity, this would result in an<br />

annual production of 46 egg cases. This is a relatively high reproductive output for a<br />

chondrichthyan. Richardson et al. (2000) suggested that fecundity is high in H. regani, based<br />

on the proportion of mature females carrying egg cases and a continuous reproductive cycle.<br />

Fecundity in other scyliorhinids may however, be low, particularly the viviparous and<br />

multiple oviparous species, where embryos or egg cases are retained for extended periods in<br />

the uterus.<br />

Catsharks generally reproduce throughout the year, and while most species lack significant<br />

patterns of reproductive seasonality, there are often seasonal peaks in egg production. (Ebert<br />

et al. 2006). Richardson et al. (2000) suggested continuous year-round reproduction in<br />

Holohalaelurus regani with no significant difference observed in the proportion of mature<br />

females carrying egg cases between seasons, similar to the situation observed in Bythaelurus<br />

dawsoni (Francis 2006). Cross (1988) suggested that A. brunneus and P. xaniurus may be<br />

reproductively active throughout the year, although in A. brunneus more females carried egg<br />

cases in December to May than June to November. Both G. eastmani and G. nipponensis<br />

from Suruga Bay, Japan reproduced throughout the year, but with G. nipponensis showing a<br />

higher incidence of carrying egg cases in December and January (Horie and Tanaka 2000).<br />

Off southern Portugal, G. melastomus is reproductively active year-round but with bimodal<br />

peaks, in summer and winter (Costa et al. 2005).<br />

Estimates of maturity for G. melastomus have shown a high degree of consistency in the<br />

western and central Mediterranean (Tursi et al. 1993, Ungaro et al. 1997, Rey et al. 2004), but<br />

maturity appears to occur at a considerably larger size in the NE Atlantic, demonstrated by a<br />

study off Portugal (Costa et al. 2005). It should be noted that Table 2.11 provides a summary<br />

of only a handful of maturity estimations for G. melastomus from the Mediterranean and these<br />

are reviewed more comprehensively in Table 4 of Costa et al. (2005). Castro et al. (1988)<br />

suggested that there may be geographical variation in size at maturity for the chain dogfish<br />

Scyliorhinus retifer, and this was indeed supported by Sminkey and Tabit (1992) who<br />

documented smaller maturity in the northern part of the species' distribution.<br />

There is a complete lack of age and growth estimates for deepwater scyliorhinids, and the<br />

vertebrae of many species may be to poorly calcified to yield age estimates (S. Irvine pers.<br />

comm.). Tursi et al. (1993) suggested, without quantitative data, that maturity is probably<br />

reached in G. melastomus at around 3–4 years, and that maximum size corresponds to at least<br />

7–8 years. Attempts to age Apristurus brunneus, A. kampae and Parmaturus xaniurus by<br />

researchers at the Pacific <strong>Shark</strong> Research Center at Moss Landing Marine Laboratories have<br />

proved unsuccessful (B. Flammang, pers. comm.).<br />

84

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