The use of cephalopod beaks in ecological and population dynamics studies has allowed major advances of our knowledge on the role of cephalopods in marine ecosystems in the last 60 years. Since the 1960’s, with the pioneering research by Malcolm Clarke and colleagues, cephalopod beaks (also named jaws or mandibles) have been described to species level and their measurements have been shown to be related to cephalopod body size and mass, which permitted important information to be obtained on numerous biological and ecological aspects of cephalopods in marine ecosystems. In the last decade, a range of new techniques has been applied to cephalopod beaks, permitting new kinds of insight into cephalopod biology and ecology. The workshop on cephalopod beaks of the Cephalopod International Advisory Council Conference (Sesimbra, Portugal) in 2022 aimed to review the most recent scientific developments in this field and to identify future challenges, particularly in relation to taxonomy, age, growth, chemical composition (i.e., DNA, proteomics, stable isotopes, trace elements) and physical (i.e., structural) analyses. In terms of taxonomy, new techniques (e.g., 3D geometric morphometrics) for identifying cephalopods from their beaks are being developed with promising results, although the need for experts and reference collections of cephalopod beaks will continue. The use of beak microstructure for age and growth studies has been validated. Stable isotope analyses on beaks have proven to be an excellent technique to get valuable information on the ecology of cephalopods (namely habitat and trophic position). Trace element analyses is also possible using beaks, where concentrations are significantly lower than in other tissues (e.g., muscle, digestive gland, gills). Extracting DNA from beaks was only possible in one study so far. Protein analyses can also be made using cephalopod beaks. Future challenges in research using cephalopod beaks are also discussed.
Loliginid squids of the Sepioteuthis lessoniana complex are widely spread in the Indo-Pacific Ocean, where they constitute a commercially important resource for neritic fisheries. Sepioteuthis lessoniana is the only Lessepsian squid migrant till now, recorded for the first time in the Mediterranean in 2002 along the Turkish Levantine coasts. Two maturing males, with mantle lengths 193 mm and 244 mm, have been recently caught near the coasts of Rhodes Island (SE Aegean), extending the species distribution northward, into Hellenic waters. Their identity was confirmed by comparison of the main body, beak characteristics and morphometric measurements with those available in the literature for this species. Suspected expansion of the Lessepsian loliginid into the Aegean Sea, due to the gradual warming of the sea, is discussed.
This study concerns the cephalopod species that are part of the diet of the small-spotted catshark Scyliorhinus canicula and the longnose spurdog Squalus blainville sampled by commercial trawlers in the Aegean Sea from 2005 to 2012. Based on the examined cephalopod beaks, 15 species were identified belonging in six families of Teuthida, one of Sepiida and two of Octopoda. The diversity of cephalopod prey species was higher for S. canicula (N = 15) than for S. blainville (N = 10). Nektonic cephalopods comprised the majority (>72%) of the preyed species by both sharks, among which about 55% inhabit the demersal zone and 45% the mesopelagic. In the diet of S. canicula, the demersal squid Illex coindetii and the pelagic sepiolid Heteroteuthis dispar were equally represented composing 20% of prey specimens, followed by the small-sized squid Abralia veranyi and the demersal sepiolid Rossia macrosoma. The latter species was substituted in the diet of S. blainville by the demersal medium-sized octopod Scaeurgus unicirrhus, which with the equally represented three other species, composed 50% of the cephalopod prey. Differences observed between S. canicula and S. blainville in the condition of beaks retained in their stomach contents and in the variation of prey species diversity by predator specimen size, may imply differences in their foraging tactics (hunting for prey vs scavenging on the bottom), habitats and stomach evacuation frequency.
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