The Permo-Carboniferous eurynotiforms show conspicuous modifications to postcranial and cranial morphology relative to primitive actinopterygian conditions, and represent an important early example of functional experimentation within ray-finned fishes. Although eurynotiforms are represented by abundant articulated fossil material, the internal anatomy of the group is not well known. Microcomputed tomography (μCT) of Eurynotus crenatus from the early Carboniferous (Viséan) Wardie Shales Member of the Gullane Formation of Wardie, Scotland provides detailed information on the jaws, palate and dentition. The lower jaw is deep and bears a well-developed convex dental plate on the prearticular/coronoids. The dentary bears a dorsally directed posterior process and lacks any obvious marginal dentition. The prearticular bears a low coronoid process. Apart from the first and second dermopalatines, and a likely accessory vomer, bones of the palate are tightly sutured or fused. The upper dental plate comprises a longitudinal, concave horizontal dental surface that occludes with the convex lower toothplate, and a more vertical region consisting of anastomosing ridges. The parasphenoid has a narrow anterior corpus and a broad posterior stalk that bears a pronounced midline notch. The smooth, irregularly punctated surfaces of the dental plates are formed by closely packed teeth with conjoined crowns, providing clues to the evolution of the more monolithic toothplates of Amphicentrum from the peg-like teeth reported in the earliest and most anatomically generalised eurynotiforms. The feeding apparatus shows many qualitative and quantitative features consistent with the processing of hard prey items. Eurynotus and its relatives show the first clear example of jaw and dental structures consistent with durophagy among actinopterygians. The origin of the group in the early Carboniferous is suggestive of diversification into newly available ecological roles in the aftermath of the end-Devonian extinction.

Crabs are thought to play a vital role in structuring gastropod populations. Studies quantifying the frequencies with which crabs attack gastropods in natural settings are, however, scarce. Although a wide variety of techniques exist with which predator–prey interactions can be investigated (e.g. laboratory experiments, exclusion caging, tethering and population surveys), there is a need for methods that can provide large amounts of quantitative data, particularly documenting the frequency with which crabs attack gastropods. This study examines the utility of using wax replicas of gastropods to determine crab attack frequencies. Replicas of Chlorostoma funebralis, Nucella ostrina and Nucella lamellosa were bolted to mesh screens and deployed in the rocky intertidal. Crabs attacked wax replicas of gastropods, leaving characteristic marks in the wax. In most cases, the appendage used in the attack could be identified from the marks (i.e. chelae vs walking legs). The effectiveness of this technique was verified using surveys of repair scar frequencies of the gastropod populations; patterns in attack frequency, determined from the number of marked wax replicas, were consistent with those of repair frequency, in that both were greater at the wave protected, quiet water locality. This study confirms the value of wax replicas in investigations of crab predation to determine the frequency and type of attack, and illustrates the potential of this method for quantifying predation intensity. The development of techniques that quantify the magnitude and exact nature of the effects of crab predation on intertidal communities is pivotal, given the intensity of commercial fishing of some species of crabs.

Field observations of small (<20 mm) individuals of Mytulus galloprovincialis at Littlehampton (West Sussex) on the south-eastern coast of England showed that many collected as recently dead shells had a distinctive pattern of damage around the posterior valve margins. Laboratory experiments confirmed that small Carcinus maenas (<22 mm carapace width) were capable of inflicting a similar style of damage. Small C. maenas fed successfully on a range of mussel sizes (5–20 mm shell length), positively correlated with carapace width. All used the same technique to access the bivalve prey, that is, by marginal mandibular chipping in order to achieve sufficient damage to allow insertion of a chelal dactyl between the valves. Mandibular chipping has previously been reported upon from non-chelate decapods and juvenile lobsters. The chelae of juvenile C. maenas are small and have a lower mechanical advantage than has been reported upon for adult conspecifics which, in any case, are not highly adapted for durophagy. We suggest that because of the poor mechanical performance and small gape of the chelae juvenile C. maenas behave as though they were achelate. As well as broadening our understanding of the repertoire of known feeding behaviours of C. maenas, our study may also provide an insight into the evolution of durophagy within the Decapoda.

Recent data have shown that owing to their seed-predator capacity Chiroderma doriae and Chiroderma villosum trophically depart from all previously studied species within the canopy fruit-bat ensemble. In this paper, the hypothesis that morphological adaptations related to granivory have evolved in these bats is investigated and discussed. A canonical variate analysis was used to search for possible divergent trends between the masticatory apparatus of Chiroderma and other stenodermatines currently recognized in the same ensemble. A total of 142 specimens representative of eight species was included in the analysis. Species of Chiroderma can be discriminated from all other species in the sample based on the increased development of masseter-related variables (height of the anterior zygomatic arch, masseter moment arm, and masseter volume), which, in conjunction with other morphological characteristics (dentition and gape angle) discussed herein, corroborates the evolution of durophagy in this group. A complementary analysis based on a Mantel test revealed that the pattern of morphological differentiation that emerged from the canonical variate analysis does not agree with the one expected based solely on the phylogenetic relationships adopted for the canopy fruit-bats studied here. This result is consistent with the hypothesis that morphological adaptations related to granivory have evolved in Chiroderma.