This paper presents a review of recent developments in the study of vision in fossil arthropods, beginning with a discussion of the origin of visual systems. A report of the eyes of Cambrian arthropods from different Lagerstätten, especially the compound and median arthropod eyes from the Chengjiang fauna of China, is given. Reference is made also to compound eyes from the lower Cambrian Emu Bay Shale fauna of Australia and the Sirius Passet fauna of Greenland; also to the three-dimensionally preserved ‘Orsten’ fauna of Sweden. An understanding of how these eyes functioned is possible by reference to living arthropods and by using physical tools developed by physiologists. The eyes of trilobites (lower Cambrian to Upper Permian) are often very well preserved, and the structure and physiology of their calcite lenses, and the eye as a whole, are summarised here, based upon recent literature. Two main kinds of trilobite eyes have been long known. Firstly, there is the holochroal type, in which the lenses are usually numerous, small and closely packed together; this represents the ancestral kind, first found in lowermost Cambrian trilobites. The second type is the schizochroal eye, in which the lenses are relatively much larger and each is separated from its neighbours. Such eyes are confined to the single suborder Phacopina (Lower Ordovician to Upper Devonian). This visual system has no real equivalents in the animal kingdom. In this present paper, the origin of schizochroal eyes, by paedomorphosis from holochroal precursors, is reviewed, together with subsequent evolutionary transitions in the Early Ordovician. A summary of new work on the structure and mineralogy of phacopid lenses is presented, as is a discussion of the recent discovery of sublensar sensory structures in Devonian phacopids, which has opened up new dimensions in the study of trilobite vision.

The bivalve ligament provides the thrust for shell opening, acting as the resistance in a lever system against which adductor muscle effort is applied. Usually, its outer lamellar layer is subjected to tensile stress, while the inner fibrous layer is compressed, with the pivotal axis located between them. However, opisthogyrate rostrate bivalves display a concave dorsal margin, and both the umbo and the postero-dorsal angle of the shell project dorsally to the ligament, which then fails to act as pivotal axis. Three opisthogyrate rostrate genera of unrelated lineages show somewhat different solutions to this morpho-functional challenge. In Cuspidaria (Anomalodesmata), the ligament is internal, subjected only to compression and ventral to the pivotal axis, a thickened periostracum develops, forcing the dorsal margins of the valves to act as pivotal axis, and the posterior parts of the shell's dorsal margins gape dorsally. In Nuculana (Palaeotaxodonta), the inner layer of the ligament is internal, the outer layer is external but reduced, and some species develop a dorsal ridge parallel to the commissural plane, on a level with the rostrum and acting as pivotal axis. In Pterotrigonia (Palaeoheterodonta) and other rostrate trigoniides, the ligament is external opisthodetic, but is allometrically reduced. Trigoniides may also develop a dorsal ridge.

Little is known about the tooth wear of South American theropod dinosaurs. This paper describes wear facets in Abelisauridae, Carcharodontosauridae and some indeterminate theropods teeth, from the Marília Formation. Four types of wear facets are proposed: vertically-oriented attritional striations; perpendicular attritional surfaces; oval wear facets; and apical grooves. All these worn surfaces were produced by dental occlusion, except the apical grooves, which are produced by the contact between predator teeth and the prey bone during predator–prey interaction. More detailed biomechanical and hardness testing of teeth and bone may further elucidate the pattern of tooth wear in theropods.

Morphological studies of the braincase and cranial endocast of fossil crocodylians, especially gavialids, are scarce. Here, we present a detailed description of the neuroanatomy of Gryposuchus neogaeus from the Miocene of Argentina, based on CT scans. The cranial endocast is sub-horizontal and the angle formed between the mid-brain and the hind-brain is poorly marked. When compared with Gavialis gangeticus, the mid-brain of G. neogaeus is relatively shorter, although the distribution of cranial nerves is similar. In the floor of the endocranial cavity, posterior to the dorsum sellae, there is a median foramen that leads into a canal that runs anteroventrally through the basisphenoid to penetrate the posterior wall of the pituitary fossa (open foramen for the basilar artery?). The same structure is present in G. gangeticus, but is absent in other living crocodylians, suggesting a potential synapomorphy of Gavialoidea. The pneumaticity of the skull roof and the lateral branches of the pharyngotympanic system in G. neogaeus are markedly reduced when compared with the extant species. Comparisons with the living Gavialis indicate that the pattern of braincase morphology of Gavialidae was present in the Miocene; however, the internal morphology, including brain shape, pneumaticity of the skull roof and basicranium, is different in the two species. This work is the first step to understand the variation of the neuroanatomy in this group of archosaurs and its palaeobiological implication.

Morphological and physiological features indicate Metriorhynchidae as the only group of crocodylomorphs with a pelagic lifestyle. Some of these features have evolved convergently in several clades of tetrapods secondarily adapted to aquatic life. One striking feature of metriorhynchids as compared to other crocodylomorphs is the morphology of the pelvic region (i.e., ventrally deflected sacral ribs and reduced pelvic girdle), which increases significantly the depth of this region. This morphology, as a whole, resembles that of other viviparous Mesozoic marine reptiles not phylogenetically related to metriorhynchids. We tested two alternative hypotheses of reproductive strategies in this clade: oviparity vs. viviparity. Given the lack of direct evidence supporting one or the other, we explored the use of evidence that may disconfirm either of these hypotheses. Using this counter-inductive approach, we found no cases contradicting viviparity in metriorhynchids, except for their phylogenetic position as archosaurs. A survey of reproductive modes amongst amniotes depicts the evolutionary plasticity of the transition to viviparity, and a widespread occurrence among tetrapods secondarily adapted to a marine life. Assuming oviparity for metriorhynchids implies egg-laying out of the water. However, their postcranial morphology (i.e., features of fore and hind limbs, pelvic girdle, and tail) contradicts this possibility. In this context, we rejected oviparity for metriorhynchids.

The hind limbs of birds have long been considered a key feature in the conquest of different environments. However, the high level of morphological diversity encountered complicates the foundation of a good theoretical correlation between morphology, locomotor habits and substrate preference and this, in turn, complicates palaeobiological interpretations. Phorusrhacids (Aves, Cariamiformes) are a good example, since they have been unequivocally categorised as terrestrial birds due to their reduced forelimbs; and as apex predators with the ability to pursue prey based only on their hind limb morphology. Multivariate techniques (PCA and discriminant analysis), based on traditional metrics and geomorphometrics of the hind limb and pelvis, were applied in order to explore terrestriality and cursoriality in phorusrhacids. Although several groups of birds could be identified, when looking solely at hind limb metrics, some phorusrhacids appear to be associated with walking birds, while others are associated with cursorial birds. However, the pelvis separates cursorial birds and phorusrhacids from walking and wading birds. This scenario is complicated further by a lack of clear definition of the different locomotor modes and substrate preferences in extant birds, and this makes it difficult to confirm phorusrhacid cursoriality based solely on morphometrics. However, some qualitative features of the pelvis and foot make the picture a little clearer. To study limb adaptations in fossil birds, a more holistic study, with an emphasis on qualitative features of the whole posterior locomotor module, is necessary, since morphometrics leaves some issues unresolved. A comparison with the wings is also needed, in order to make a more complete analysis of locomotor behaviour.

Sparassodonta is a diverse group of extinct metatherian predators that include forms with diets ranging from omnivores to hypercarnivores, including potential bone-crushers and sabre-tooth specialised species. Most of the previous dietary studies on the group were based on qualitative approaches or dental morphometric indexes and/or bite force estimations. In this study, we explore the evolution of mandible shape and diet of Sparassodonta in a comparative phylogenetic framework, using geometric morphometric tools and allometric and discriminant analyses. We analysed the mandible shape of 142 extant species of marsupials and placental carnivores, and 15 fossil sparassodont species. We found that the relationship between shape and size of the mandible is strongly structured by phylogeny, where the more derived borhyaenoids tend to possess stronger and larger mandibles. Derived borhyaenoid sparassodonts and basal borhyaenoids were classified as hypercarnivores (with short and robust mandibular body). Hathliacynid were classified as mesocarnivores or as hypercarnivores, but with lower probabilities and less specialised morphologies (with a long and slender mandible). Although dental morphology suggests that most of the species of Sparassodonta would have been hypercarnivores, the robustness of the mandible seems to be informative regarding the prey size and degree of specialisation. The relationship between mandibular size and shape, and talonid/trigonid relative size, is strongly influenced by the phylogenetic legacy, suggesting that ecological factors could have influenced the evolution of the sparassodonts.

Pilosa include anteaters (Vermilingua) and sloths (Folivora). Modern tree sloths are represented by two genera, Bradypus and Choloepus (both around 4–6 kg), whereas the fossil record is very diverse, with approximately 90 genera ranging in age from the Oligocene to the early Holocene. Fossil sloths include four main clades, Megalonychidae, Megatheriidae, Nothrotheriidae, and Mylodontidae, ranging in size from tens of kilograms to several tons. Modern Vermilingua are represented by three genera, Cyclopes, Tamandua and Myrmecophaga, with a size range from 0.25 kg to about 30 kg, and their fossil record is scarce and fragmentary. The dependence of the body size on phylogenetic pattern of Pilosa is analysed here, according to current cladistic hypotheses. Orthonormal decomposition analysis and Abouheif C-mean were performed. Statistics were significantly different from the null-hypothesis, supporting the hypothesis that body size variation correlates with the phylogenetic pattern. Most of the correlation is concentrated within Vermilingua, and less within Mylodontidae, Megatheriidae, Nothrotheriidae and Megalonychidae. Influence of basal metabolic rate (BMR), dietary habits and substrate preference is discussed. In anteaters, specialised insectivory is proposed as the primary constraint on body size evolution. In the case of sloths, mylodontids, megatheriids and nothrotheriids show increasing body size through time; whereas megalonychids retain a wider diversity of sizes. Interplay between BMR and dietary habits appears to be the main factor in shaping evolution of sloth body size.

Notoungulates, native South American fossil mammals, have been recently objective of several palaeoecological studies. Ecomorphology and biomechanics of the masticatory apparatus, together with micro and mesowear analyses on tooth enamel, were applied in order to understand their palaeobiology. In particular, the relationship between some dental traits (hypsodonty, occlusal surface area and complexity) and body mass is still poorly understood. These features were measured by means of the hypsodonty index (HI), occlusal surface area (OSA) and tooth area (OTA), enamel crest complexity (ECC) and length (OEL). The relationships between these indices were evaluated in five pan-contemporaneous Santacrucian Notoungulata genera from Patagonia: Adinotherium and Nesodon (Toxodontia), Interatherium, Protypotherium and Hegetotherium (Typotheria). While OSA, OTA and OEL were size dependent and strongly correlated, HI and ECC were size independent. All notoungulates analysed have very hypsodont teeth, indicating high rates of tooth wear in response to an increase of abrasives consumed with the food; their tooth occlusal area and complexity could be related to chewing efforts associated with the toughness of the plants consumed. HI, OSA and ECC were considered useful for palaeoecological reconstructions, but the results presented here show that these three features are integrated as a complex, so should not be evaluated separately.

Articular surfaces reflect the relative movements between adjacent bones, and the ones involved in the elbow joint provide information about forelimb movements and may be useful for making inferences about the substrate use. The proximal articular surface of the ulna was examined through 3-D geometric morphometrics, in order to assess its usefulness as a proxy for paleoecological interpretations; particularly for two small mammals from the early Miocene of Patagonia. The sample was composed of 22 extant small mammals (rodents, carnivorans and primates) and two extinct typotheres: Hegetotherium mirabile (Hegetotheriidae) and Interatherium robustum (Interatheriidae). Forty-five landmarks were taken and principal component analysis (PCA) was used to explore the morphospace structure. The results of PCA for the whole surface were inconclusive; therefore, successive analyses were made, subdividing the surface into sub-units. The PCA for the proximal part of the trochlear notch was the most informative, allowing the recognition of morphospaces with functional value: one for digging rodents and another for most climbers. Neither typothere would have had a specialisation for climbing or digging in the features analysed. This study allows morphological patterns on different parts of a joint to be detected; interpreted, at least partially, as differential responses to different kinds of mechanical stress.

The procyonid †Cyonasua is endemic to South America and recorded from the Late Miocene to the Early Pleistocene. This paper studies the forelimb of †Cyonasua sp. (late Pliocene of Miramar, Argentina), using an ecomorphological approach to infer morphological adaptations linked to substrate preference and locomotory mode, as well as to grasping and digging ability. Twenty linear measurements of forelimb and pectoral girdle were taken from †Cyonasua sp. and a sample of 87 specimens of extant carnivoran families (Procyonidae, Mustelidae, Ursidae, Viverridae, Canidae and Felidae). Raw values were transformed to minimise the effect of size. Morphological variation was explored by principal component analysis (PCA); substrate preference and locomotory mode were further analysed by multivariate analysis of variance (MAV) and discriminant analysis (DA); grasping and digging ability were analysed by DA. In the PCA morphospace, †Cyonasua sp. occupied a unique position, close to extant procyonids. DA classified it as non-specialised digger with poor grasping ability. The results lead to the interpretation of †Cyonasua sp. as having a moderately stabilised elbow joint with poor pronation–supination, although some climbing skills cannot be ruled out. Thus, †Cyonasua sp. could have had generalised habits, in agreement with reconstructed palaeoenvironmental conditions.

The morphology of the mastoid region in predators is informative about the hunting strategies and capacity of carrying prey. The purpose of this research was to describe the mastoid region and reconstruct the associated musculature of †Stipanicicia pettorutii Reig, 1956, a Pleistocene weasel with a distinctive morphology compared to its living relatives, and to make inferences about its predatory abilities. Galictis, a living weasel closely related to Stipanicicia, as well as other carnivorans, were used as comparative models. The muscle insertions identified in Stipanicicia presented a similar or larger development than Galictis. The insertion area of the muscles obliquus capitis cranialis, longissimus capitis, sternocephalicus pars mastoidea and cleidocephalicus pars mastoidea were found to be markedly developed and in a lateralised position with respect to the atlanto–occipital joint in hyaenids and mustelids, and especially in Stipanicicia, suggesting powerful lateral flexion and rotation movements in the fossil. The larger degree of advancement of the mastoid process in mustelids, and secondary in felids, would allow a powerful ventral flexion of the head. Stipanicicia would have exhibited powerful lateral movements and retraction of the head and neck, over restricted extension movements and, therefore, would have been a weasel specialised in subjugating and carrying prey of a relatively large size.