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In September, 2016, an adult female blue shark (Prionace glauca) 247 cm long stranded alive on the coast of Valencia (Spain, Western Mediterranean) but died shortly afterwards. The necropsy revealed ongoing pregnancy, with 65 embryos in early stage of development, and a healthy condition with no signs of starvation. Two fishing hooks surrounded by scarred tissue were detected in the mandible, indicating past interaction with fisheries. In addition, a fragment of the tip of a swordfish (Xiphias gladius) rostrum (length: 18 cm long, width: 0.5 cm (distal) and 3 cm (proximal)) was removed from the animal. The fragment had pierced the head producing an incision of 3.5 cm close to the left eye, crossing the head anterior to the pre-orbital process. No apparent damage was observed in the olfactory capsule or the eye, but the fragment had penetrated both sides of the skull causing extensive lesions in the brain, which were inferred to be the cause of death. Allometric analysis suggested that the swordfish was ca. 110 cm long, corresponding to a juvenile 1-2 yrs old. Swordfish had previously been reported driving their rostrum into pelagic sharks, allegedly as a defensive strategy. However, this is the first report of impalement as the direct cause of death in blue sharks.

There are numerous reports of billfishes spearing objects, marine organisms, and even humans. Whether or not this behaviour is intentional and, if so, what is its functional meaning, are open questions. In 2016, an adult blue shark (Prionace glauca) was found to be killed by a juvenile swordfish (Xiphias gladius) in the western Mediterranean. Here we report on three more recent cases involving both species in the same area. In February 2017, an adult male blue shark was found stranded in Garrucha (Spain) with a fragment of a juvenile swordfish’s rostrum (18cm long x 2cm wide at proximal end) inserted in its cranium. In March 2017, an adult pregnant female blue shark was stranded alive on the coast of Ostia (Italy) but died shortly afterwards; a fragment of a juvenile swordfish’s rostrum (25x3cm) was found allocated between the eye and the cranium. Finally, in February 2018, an adult female blue shark appeared stranded in the coast of Vera (Spain), with a putative impalement injury anterior to the right eye but without an associated bill fragment. Surprisingly, X-ray and computed tomography revealed an older injury in the right nostril, with a small piece of a juvenile swordfish’s rostrum (5.3x1.2cm). These cases suggest that juvenile swordfish would drive their rostrum into blue sharks as a defensive strategy that is likely to be far from anecdotal. We suggest that no regular cases of these interactions are reported because they occur at high sea and evidence of them, when available, can easily be overlooked.

Large oceanic sharks represent a suitable model to investigate the influence of a host's oceanic conditions on the structure of its helminth communities. In this study, we describe the intestinal helminth fauna, and investigate determinants of infracommunity structure, in 39 specimens of shortfin mako Isurus oxyrinchus collected in the NE Atlantic. Six cestode species were found in the spiral valve of makos: 3 are typical from lamnid sharks, namely, gravid specimens of Clistobothrium montaukensis, Gymnorhynchus isuri and Ceratobothrium xanthocephalum, and 3 are immature specimens of cestode species common to several elasmobranchs, namely, Dinobothrium septaria, Nybelinia lingualis, and Phyllobothrium cf. lactuca. In addition, L3 larvae of Anisakis sp. type I were detected. Infracommunities were species poor and had low total helminth abundance. The result of Schluter's variance ratio test was compatible with the hypothesis of independent colonization of helminth taxa. These results conform to previous studies on oceanic predators that have hypothesized that these hosts should have depauperate and unpredictable helminth infracommunities because oceanic conditions hamper parasite transmission. However, mean species richness and mean total abundance of cestodes of shortfin mako and other oceanic sharks did not significantly differ from those of elasmobranchs from other habitats. This suggests that the large body size and prey consumption rates of oceanic sharks offset the negative 'dilution' effect of oceanic habitat on transmission rates. Additionally, or alternatively, parasites of oceanic sharks may have expanded the use of intermediate hosts through the trophic web to spread out the risk of failure to complete their life cycles.

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