The life histories of two globally endangered hammerhead sharks, Sphyrna lewini and Sphyrna mokarran, were examined using samples collected from a range of commercial fisheries operating along the east coast of Australia. The catch of S. lewini was heavily biased towards males, and there were significant differences in von Bertalanffy growth parameters (L(∞) and k) and maturity [stretched total length (L(ST)) and age (A) at which 50% are mature, L(ST50) and A(50)] between those caught in the tropics (L(∞) = 2119 mm, k = 0·163, L(ST50) = 1471 mm, A(50) = 5·7 years) and those caught in temperate waters (L(∞) = 3199 mm, k = 0·093, L(ST50) = 2043 mm, A(50) = 8·9 years). The best-fit estimates for a three-parameter von Bertalanffy growth curve fit to both sexes were L(∞) = 3312 mm, L(0) = 584 mm and k = 0·076. Males attained a maximum age of 21 years and grew to at least 2898 mm L(ST). The longevity, maximum length and maturity of females could not be estimated as mature animals could not be sourced from any fishery. Length at birth inferred from neonates with open umbilical scars was 465-563 mm L(ST). There was no significant difference in length and age at maturity of male and female S. mokarran, which reached 50% maturity at 2279 mm L(ST) and 8·3 years. Sphyrna mokarran grew at a similar rate to S. lewini and the best-fit estimates for a two-parameter von Bertalanffy equation fit to length-at-age data for sexes combined with an assumed mean length-at-birth of 700 mm were L(∞) = 4027 mm and k = 0·079. Females attained a maximum age of 39·1 years and grew to at least 4391 mm L(ST). The oldest male S. mokarran was 31·7 years old and 3691 mm L(ST). Validation of annual growth-band deposition in S. mokarran was achieved through a mark, tag and recapture study.

Abstract. The life histories of small-bodied coastal sharks, particularly carcharhinids, are generally less conservative than those of large-bodied species. The present study investigated the life history of the small-bodied slit-eye shark, Loxodon macrorhinus, from subtropical Hervey Bay, Queensland, and compared this species' biology to that of other coastal carcharhinids. The best-fit age model provided parameters of L N ¼ 895 mm total length (TL), k ¼ 0.18 and t 0 ¼ À6.3 for females, and L N ¼ 832 mm TL, k ¼ 0.44 and t 0 ¼ À2.6 for males. For sex-combined data, a logistic function provided the best fit, with L N ¼ 842 mm TL, k ¼ 0.41 and a ¼ À2.2. Length and age at which 50% of the population was mature was 680 mm TL and 1.4 years for females, and 733 mm TL and 1.9 years for males. Within Hervey Bay, L. macrorhinus exhibited an annual seasonal reproductive cycle, producing an average litter of 1.9 AE 0.3 s.d. With the exception of the low fecundity and large size-at-birth relative to maximum maternal TL, the life-history traits of L. macrorhinus are comparable to other small-bodied coastal carcharhinids, and its apparent fast growth and early maturation contrasts that of large-bodied carcharhinids.

Total lengths (L(T)) at age and growth rates for south-west Pacific Galeocerdo cuvier were estimated from vertebral growth-band counts of 202 sagitally sectioned centra from 112 females (71-430 cm L(T)), 79 males (72-351 cm L(T)) and 11 of unknown sex. Captive growth data were also examined to complement vertebral age estimations. The sexes combined modelled growth coefficient (k = 0.08) was smaller than previously reported for G. cuvier populations elsewhere. Split-band and narrow banding patterns were identified as potential sources of age underestimation in this species.

Unlike other elasmobranchs, batoids exhibit sexually dimorphic dentition. The functional implications of such dentition, however, remain understudied. For the present study, ontogenetic and sexual dimorphism in tooth and jaw structure, together with the functional implications of this dimorphism, were determined in the eastern shovelnose ray, Aptychotrema rostrata. Sexually dimorphic dentition and jaw structure was first observed in sub-adult age classes, with males developing a pronounced lower jaw at the symphysis. Monognathic heterodonty was prominent in mature males, with teeth in the symphyseal region developing significantly greater heights and sharpness ratios in comparison to females. Ex vivo mechanical grip strength tests were used to determine simulated bite-grip tenacity. The mean peak pull-out forces required to withdraw a section of a dissected pectoral fin from between jaws closed with a constant occlusal force was highest for mature males, intermediate for mature females and lowest for immature females and males. Although the species exhibits ontogenetic variations in diet, these were unrelated to sex. Rather, the larger and highly cuspidate teeth of mature males increased the bite-grip tenacity, which likely aids in copulation.

An elasmobranch survey of sub-tropical Hervey Bay, Australia, captured the slit-eye shark Loxodon macrorhinus at only one of three sites sampled. The dietary composition of this small shark species was compared to the prey communities within Hervey Bay to test whether prey availability was driving this observation. Dietary analysis of prey groups revealed that teleosts dominated the diet, per cent index of relative importance, % I(RI) (79·5%) and per cent geometric index of importance, % G(II) (52·7%), with shrimp-like invertebrates and cephalopods identified as the most important invertebrate prey groups. Baited remote underwater video (BRUV) used to sample prey communities at each site, demonstrated a highly diverse and significantly different community composition among the sites. There was no significant overlap between the diet of L. macrorhinus and any of the prey communities detected by BRUVs according to one-way analysis of similarities and the simplified Morisita index. Habitat electivity analysis revealed affinity of L. macrorhinus for the site with the highest water clarity (Secchi disc depth), opposing that of three other shark species. Overall, the results suggest that the distribution of L. macrorhinus is not driven by prey availability but other factors such as water clarity, predator avoidance or a reduction in interspecies competition.