The link between dental microwear and feeding ecology in tree sloths and armadillos (Mammalia: Xenarthra)

The Xenarthra represents an enigmatic clade of placental mammals that includes living tree sloths, armadillos, and their extinct relatives, yet certain aspects of the biology of this group remains poorly understood. Here, we use scanning electron microscopy to test the hypothesis that orthodentine microwear patterns in extant xenarthrans are significantly different among different dietary groups. In a blind analysis, microwear patterns were quantified at a magnification of 500× by two independent observers for extant species from four dietary groups (carnivore–omnivores, folivores, frugivore–folivores, and insectivores). Independent observers recovered the same relative between‐group differences in microwear patterns. Insectivores and folivores have a significantly lower numbers of scratches and greater scar widths than frugivore–folivores and carnivore–omnivores, yet we were neither able to statistically distinguish insectivores from folivores, nor differentiate frugivore–folivores from carnivore–omnivores. Nevertheless, a clear distinction exists between taxa from the same trophic level and habitat, which suggests that orthodentine microwear reflects niche partitioning and habitat more than diet among related forms. We suggest that bite force and chewing mechanics have a strong influence on the formation of orthodentine microwear, which may explain some of the observed overlap between distinct groups (e.g. frugivore–folivores versus carnivore–omnivores). This study serves as a positive step forwards in our understanding of the ecological role of living xenarthrans, and serves as a foundation for using orthodentine microwear to reconstruct palaeoecology in extinct ground sloths, glyptodonts, and pampatheres. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ?? , ??–??.     

Phylogenetic relationships among sloths (Mammalia, Xenarthra, Tardigrada): the craniodental evidence

This study is undertaken in order to evaluate specific hypotheses of relationship among extant and extinct sloths (Mammalia, Xenarthra, Tardigrada). Questions of particular interest include the relationship among the three traditional family groupings of extinct ground sloths and the monophyletic or diphyletic origin of the two genera of extant tree sloths. A computer‐based cladistic investigation of the phylogenetic relationships among 33 sloth genera is performed based upon 286 osteological characteristics of the skull, lower jaw, dentition and hyoid arch. Characters are polarized via comparisons with the following successive outgroups, all members of the supraordinal grouping Edentata: the Vermilingua, or anteaters; the Cingulata, or armadillos and glyptodonts; the Palaeanodonta; and the Pholidota, or pangolins. The results of the analysis strongly corroborate the diphyly of living tree sloths, with the three‐toed sloth Bradypus positioned as the sister‐taxon to all other sloths, and the two‐toed sloth Choloepus allied with extinct members of the family Megalonychidae. These results imply that the split between the two extant sloth genera is ancient, dating back perhaps as much as 40 Myr, and that the similarities between the two taxa, including their suspensory locomotor habits, present one of the most dramatic examples of convergent evolution known among mammals. The monophyly of the three traditional ground sloth families Megatheriidae, Megalonychidae and Mylodontidae is confirmed in the present study, and the late Miocene–Pleistocene nothrotheres are shown to form a clade. It is suggested that this latter clade merits recognition as a distinct family‐level grouping, the family Nothrotheriidae. The monophyly of the Megatherioidea, a clade including members of the families Megatheriidae, Megalonychidae and Nothrotheriidae, is also supported. Within Megatherioidea, the families Nothrotheriidae and Megatheriidae form a monophyletic group called the Megatheria. The relationships within the families Megatheriidae and Mylodontidae are fully and consistently resolved, although the hypothesized scheme of relationships among the late Miocene to Pleistocene members of the mylodontid subfamily Mylodontinae differ strongly from any proposed by previous authors. Within the family Megalonychidae, Choloepus is allied to a monophyletic grouping of West Indian sloths, although the relationships within this clade are not fully resolved. © 2004 The Linnean Society of London, Zoological Journal of the Linnean Society, 2004, 140 , 255–305.     

Feeding Ecology in Oligocene Mylodontoid Sloths (Mammalia,Xenarthra) as Revealed by Orthodentine Microwear Analysis

Recently, dental microwear analysis has been successfully employed to xenarthran teeth. Here, we present new data on use wear features on 16 molariforms of Orophodon hapaloides and Octodontotherium grande. These taxa count among the earliest sloths and are known from the Deseadan SALMA (late Oligocene). Modern phylogenetic analyses classify Octodontotherium and Orophodon within Mylodontoidea with whom they share lobate cheek teeth with an outer layer of cementum and a thick layer of orthodentine. Similar target areas of 100μm² were analyzed on the orthodentine surface of each tooth by stereomicroscopic microwear and by SEM microwear. Results were unlike those of extant sloths (stereomicroscopic microwear: Bradypus, Choloepus) and published data from fossil sloths (SEM microwear: Acratocnus, Megalonyx, Megatherium, Thinobadistes); thus, both approaches independently indicate a different feeding ecology for the Oligocene taxa. The unique microwear results suggest that both taxa fed on plant material with low to moderate intrinsic toughness (foliage, twigs) but also proposes intake of tougher food items (e.g., seeds). Frequent gouging of the tooth surfaces can be explained by exogenous influence on microwear, such as possible intake of abrasive grit. We suggest an unspecialized herbivorous diet for Octodontotherium and Orophodon utilizing diverse food resources of their habitat. These interpretations support the reconstruction of (1) Deseadan environments as open habitats with spreading savannas/grasslands and (2) both taxa as wide-muzzled bulk feeders at ground level.     

Orientation of the lateral semicircular canal in Xenarthra and its links with head posture and phylogeny

The orientation of the semicircular canals of the inner ear in the skull of vertebrates is one of the determinants of the capacity of this system to detect a given rotational movement of the head. Past functional studies on the spatial orientation of the semicircular canals essentially focused on the lateral semicircular canal (LSC), which is supposedly held close to horizontal during rest and/or alert behaviors. However, they generally investigated this feature in only a few and distantly related taxa. Based on 3D‐models reconstructed from µCT‐scans of skulls, we examined the diversity of orientations of the LSC within one of the four major clades of placental mammals, that is, the superorder Xenarthra, with a data set that includes almost all extant genera and two extinct taxa. We observed a wide diversity of LSC orientations relative to the basicranium at both intraspecific and interspecific scales. The estimated phylogenetic imprint on the orientation of the LSC was significant but rather low within the superorder, though some phylogenetic conservatism was detected for armadillos that were characterized by a strongly tilted LSC. A convergence between extant suspensory sloths was also detected, both genera showing a weakly tilted LSC. Our preliminary analysis of usual head posture in extant xenarthrans based on photographs of living animals further revealed that the LSC orientation in armadillos is congruent with a strongly nose‐down head posture. It also portrayed a more complex situation for sloths and anteaters. Finally, we also demonstrate that the conformation of the cranial vault and nuchal crests as well as the orientation of the posterior part of the petrosal may covary with the LSC orientation in Xenarthra. Possible inferences for the head postures of extinct xenarthrans such as giant ground sloths are discussed in the light of these results.     

Body mass estimation in xenarthra: A predictive equation suitable for all quadrupedal terrestrial placentals?

The Magnorder Xenarthra includes strange extinct groups, like glyptodonts, similar to large armadillos, and ground sloths, terrestrial relatives of the extant tree sloths. They have created considerable paleobiological interest in the last decades; however, the ecology of most of these species is still controversial or unknown. The body mass estimation of extinct species has great importance for paleobiological reconstructions. The commonest way to estimate body mass from fossils is through linear regression. However, if the studied species does not have similar extant relatives, the allometric pattern described by the regression could differ from those shown by the extinct group. That is the case for glyptodonts and ground sloths. Thus, stepwise multiple regression were developed including extant xenarthrans (their taxonomic relatives) and ungulates (their size and ecological relatives). Cases were weighted to maximize the taxonomic evenness. Twenty‐eight equations were obtained. The distribution of the percent of prediction error (%PE) was analyzed between taxonomic groups (Perissodactyla, Artiodactyla, and Xenarthra) and size groups (0–20 kg, 20–300 kg, and more than 300 kg). To assess the predictive power of the functions, equations were applied to species not included in the regression development [test set cross validation, (TSCV)]. Only five equations had a homogeneous %PE between the aforementioned groups. These were applied to five extinct species. A mean body mass of 80 kg was estimated for Propalaehoplophorus australis (Cingulata: Glyptodontidae), 594 kg for Scelidotherium leptocephalum (Phyllophaga: Mylodontidae), and 3,550.7 kg for Lestodon armatus (Phyllophaga: Mylodontidae). The high scatter of the body mass estimations obtained for Catonyx tarijensis (Phyllophaga: Mylodontidae) and Thalassocnus natans (Phyllophaga: Megatheriidae), probably due to different specializations, prevented us from predicting its body mass. Surprisingly, although obtained from ungulates and xenarthrans, these five selected equations were also able to predict the body mass of species from groups as different as rodents, carnivores, hyracoideans, or tubulidentates. This result suggests the presence of a complex common allometric pattern for all quadrupedal placentals. J. Morphol., 2008. © 2008 Wiley‐Liss, Inc.     

Myology of the Feeding Apparatus of Myrmecophagid Anteaters (Xenarthra: Myrmecophagidae)

The musculoskeletal feeding apparatus of anteaters in the family Myrmecophagidae (Eutheria: Xenarthra) is described, compared among the three extant genera (Tamandua, Myrmecophaga, Cyclopes), and interpreted in a phylogenetic framework. Character polarities are assessed with reference to other xenarthrans, eutherians, and didelphid marsupials. Xenarthrans are widely regarded as basal eutherians, and this is reflected in the apparent retention of plesiomorphic character states in jaw and pharyngeal musculature. Jaw closing muscles are architecturally simple, the stylohyoideus is absent, the stylopharyngeus is robust and architecturally complex, and the superior pharyngeal constrictor is weak. At the same time, the highly specialized trophic ecology of myrmecophagids is reflected in derived features of the jaw, tongue, and palatal musculature. The sternomandibularis is present, the tongue is largely composed of a sternog-lossus with no attachments to the hyoid apparatus, other glossus muscles are modified and do not enter the tongue, and the mylohyoideus and stylopharyngeus contribute to the soft palate, while other palatal muscles vary among the myrmecophagid genera. Feeding apparatus mycology provides further support for myrmecophagid monophyly. Documentation of the morphological transformations that lead to the myrmecophagid condition is hampered by incomplete data on feeding apparatus structure in nonmyrmecophagid xenarthrans (sloths and armadillos) but a tentative character mapping onto an independently derived phylogeny is offered.     

Morphology of the tongue of Vermilingua (Xenarthra: Pilosa) and evolutionary considerations

The tongue of anteaters (Xenarthra, Pilosa, Vermilingua) is a highly specialized for myrmecophagy. Here, we describe the topography and histology of the tongue, and compare it to that of other xenarthrans and other myrmecophagous eutherian mammals. The tongue of Vermilingua is long and slender, with an apical protuberance, which differs between Myrmecophagidae and Cyclopes didactylus . In the former, the rostral region is conical, and in the latter, it is dorsoventrally compressed, as observed in sloths. The tongue of Vermilingua has filiform and circumvallate papillae on the surface; foliate and fungiform papillae are absent. The filiform papillae of Myrmecophaga tridactyla are simple all over the tongue, differing from Tamandua tetradactyla and Cyclopes didactylus , which present composed filiform papillae in the rostral and middle regions. Histologically, the tongue has a peculiar organization of muscular and neurovascular tissues, differing from the usual mammalian pattern. However, the tongue structure is less divergent in Cyclopes . The presence of two circumvallate papillae is common to the three major clades of Xenarthra (Cingulata, Folivora and Vermilingua). In each group, the tongue may reflect functional features related to myrmecophagous (anteaters and some armadillos), omnivorous (remaining armadillos) and folivorous (sloths) feeding habits. The similarities between the tongues of Vermiligua and other non‐xenarthran eutherian myrmecophagous mammals are somewhat general and, under close inspection, superficial, being an example of different lineages achieving the same morphofunctional adaptations through distinct evolutionary pathways.     

Muzzle of South American Pleistocene ground sloths (Xenarthra, Tardigrada)

Sloths are among the most characteristic elements of the Cainozoic of South America and are represented, during the Pleistocene, by approximately nine genera of gigantic ground sloths (Megatheriidae and Mylodontidae). A few contributions have described their masticatory apparatus, but almost no attention has been paid to the reconstruction of the muzzle, an important feature to consider in relation to food intake, and particularly relevant in sloths because of the edentulous nature of the muzzle and its varied morphology. The relationship between dietary habits and shape and width of the muzzle is well documented in living herbivores and has been considered an important feature for the inference of alimentary styles in fossils, providing an interesting methodological tool that deserves to be considered for xenarthrans. The goal of this study was to examine models of food intake by reconstructing the appearance and shape of the muzzle in five species of Pleistocene ground sloths (Megatherium americanum, Glossotherium robustum, Lestodon armatus, Mylodon darwini, and Scelidotherium leptocephalum) using reconstructions of the nasal cartilages and facial muscles involved in food intake. The preservation of the nasal septum, and the scars for muscular attachment in the rostral part of the skulls, allow making a conservative reconstruction of muzzle anatomy in fossil sloths. Wide-muzzled ground sloths (Glossotherium and Lestodon) had a square, nonprehensile upper lip and were mostly bulk-feeders. The lips, coupled with the tongue, were used to pull out grass and herbaceous plants. Narrow-muzzled sloths (Mylodon, Scelidotherium, and Megatherium) had a cone-shaped and prehensile lip and were mixed or selective feeders. The prehensile lip was used to select particular plants or plant parts.     

Trabecular architecture in the forelimb epiphyses of extant xenarthrans (Mammalia)

Background

Bone structure has a crucial role in the functional adaptations that allow vertebrates to conduct their diverse lifestyles. Much has been documented regarding the diaphyseal structure of long bones of tetrapods. However, the architecture of trabecular bone, which is for instance found within the epiphyses of long bones, and which has been shown experimentally to be extremely plastic, has received little attention in the context of lifestyle adaptations (virtually only in primates). We therefore investigated the forelimb epiphyses of extant xenarthrans, the placental mammals including the sloths, anteaters, and armadillos. They are characterised by several lifestyles and degrees of fossoriality involving distinct uses of their forelimb. We used micro computed tomography data to acquire 3D trabecular parameters at regions of interest (ROIs) for all extant genera of xenarthrans (with replicates). Traditional, spherical, and phylogenetically informed statistics (including the consideration of size effects) were used to characterise the functional signal of these parameters.

Results

Several trabecular parameters yielded functional distinctions. The main direction of the trabeculae distinguished lifestyle categories for one ROI (the radial trochlea). Among the other trabecular parameters, it is the degree of anisotropy (i.e., a preferential alignment of the trabeculae) that yielded the clearest functional signal. For all ROIs, the armadillos, which represent the fully terrestrial and fossorial category, were found as characterised by a greater degree of anisotropy (i.e., more aligned trabeculae). Furthermore, the trabeculae of the humeral head of the most fossorial armadillos were also found to be more anisotropic than in the less fossorial species.

Conclusions

Most parameters were marked by an important intraspecific variability and by a size effect, which could, at least partly, be masking the functional signal. But for some parameters, the degree of anisotropy in particular, a clear functional distinction was recovered. Along with data on primates, our findings suggest that a trabecular architecture characterised by a greater degree of anisotropy is to be expected in species in which the relevant epiphyses withstand a restricted range of load directions. Trabecular architecture therefore is a promising research avenue for the reconstruction of lifestyles in extinct or cryptic species.

     

Ungual phalanges analysis in Pleistocene ground sloths (Xenarthra,Folivora)

Ungual phalanges (the most distal bone within a limb) and claws (the overlying corneous sheath) from the third digit of the forefoot of selected Pleistocene ground sloths (Lestodon armatus, Glossotherium robustum, Scelidotherium leptocephalum and Megatherium americanum) are analysed, as well as those of some living xenarthrans for actualistic comparison, aiming at testing hypotheses of substrate usage and locomotor behaviour. The third digits were chosen for this study because of its size and nearly perfect bilateral symmetry, which increases the possibilities of revealing functional differences between taxa. The analyses performed were of inner and external curvature, the strength indicator and the mechanical advantage. The mechanical advantage indicates that the four ground sloths’ species were well adapted for strenuous activities, such as digging, in which force rather than velocity is optimised. Their strength indicator shows expected values for their body size, while in Mylodon darwinii the value obtained was lower than expected. In the two curvature analyses L. armatus, G. robustum and M. americanum fall within the group of armadillos that dig, whereas S. leptocephalum does not, this might be due to a difference in the movements performed while performing an activity such as digging or similar to it.     

Microstructure of dental hard tissues in fossil and recent xenarthrans (Mammalia: Folivora and Cingulata)

A striking difference between xenarthrans and other mammals is the complete loss of tooth enamel in all members but the earliest armadillos. However, sloth and armadillo teeth show structured wear facets, which in all other mammals are formed by tooth enamel. How is that possible? Here, I report about an analysis of fossil and recent xenarthran dental hard tissue microstructure. It shows that osteodentine is not exclusive to fossil Cingulata, but also occurs in some recent taxa. Furthermore, I found profound modifications of orthodentine architecture in comparison to other mammals. Remarkable features are (a) a larger proportion of the highly mineralized, collagen‐free peritubular dentine, and (b) a modified architecture of the odontoblastic process with frequent interconnections between the extensions and unusually intensive branching of the extensions forming a complex meshwork, penetrating the intertubular dentine matrix. The orthodentine microstructural build‐up is unique in Folivora and Cingulata. J. Morphol., 2011. © 2011 Wiley‐Liss, Inc.     

The relationship between diet and tooth complexity in living dentigerous saurians

Living saurian reptiles exhibit a wide range of diets, from carnivores to strict herbivores. Previous research suggests that the tooth shape in some lizard clades correlates with diet, but this has not been tested using quantitative methods. I investigated the relationship between phenotypic tooth complexity and diet in living reptiles by examining the entire dentary tooth row in over 80 specimens comprising all major dentigerous saurian clades. I quantified dental complexity using orientation patch count rotated (OPCR), which discriminates diet in living and extinct mammals, where OPCR‐values increase with the proportion of dietary plant matter. OPCR was calculated from high‐resolution CT‐scans, and I standardized OPCR‐values by the total number of teeth to account for differences in tooth count across taxa. In contrast with extant mammals, there appears to be greater overlap in tooth complexity values across dietary groups because multicusped teeth characterize herbivores, omnivores, and insectivores, and because herbivorous skinks have relatively simple teeth. In particular, insectivorous lizards have dental complexities that are very similar to omnivores. Regardless, OPCR‐values for animals that consume significant amounts of plant material are higher than those of carnivores, with herbivores having the highest average dental complexity. These results suggest reptilian tooth complexity is related to diet, similar to extinct and extant mammals, although phylogenetic history also plays a measurable role in dental complexity. This has implications for extinct amniotes that display a dramatic range of tooth morphologies, many with no modern analogs, which inhibits detailed dietary reconstructions. These data demonstrate that OPCR, when combined with additional morphological data, has the potential to be used to reconstruct the diet of extinct amniotes. J. Morphol. 278:500–522, 2017. © 2017 Wiley Periodicals, Inc.     

Genomic evidence for rod monochromacy in sloths and armadillos suggests early subterranean history for Xenarthra

Rod monochromacy is a rare condition in vertebrates characterized by the absence of cone photoreceptor cells. The resulting phenotype is colourblindness and low acuity vision in dim-light and blindness in bright-light conditions. Early reports of xenarthrans (armadillos, sloths and anteaters) suggest that they are rod monochromats, but this has not been tested with genomic data. We searched the genomes of Dasypus novemcinctus (nine-banded armadillo), Choloepus hoffmanni (Hoffmann''s two-toed sloth) and Mylodon darwinii (extinct ground sloth) for retinal photoreceptor genes and examined them for inactivating mutations. We performed PCR and Sanger sequencing on cone phototransduction genes of 10 additional xenarthrans to test for shared inactivating mutations and estimated the timing of inactivation for photoreceptor pseudogenes. We concluded that a stem xenarthran became an long-wavelength sensitive-cone monochromat following a missense mutation at a critical residue in SWS1, and a stem cingulate (armadillos, glyptodonts and pampatheres) and stem pilosan (sloths and anteaters) independently acquired rod monochromacy early in their evolutionary history following the inactivation of LWS and PDE6C, respectively. We hypothesize that rod monochromacy in armadillos and pilosans evolved as an adaptation to a subterranean habitat in the early history of Xenarthra. The presence of rod monochromacy has major implications for understanding xenarthran behavioural ecology and evolution.     

Articular and vertebral lesions in the Pleistocene sloths (Xenarthra,Folivora) from the Brazilian Intertropical Region

We performed a macroscopic study on six species of Pleistocene sloths from the Brazilian Intertropical Region (BIR) including Valgipes bucklandi, Catonyx cuvieri, Mylodonopsis ibseni, Glossotherium sp., Ocnotherium giganteum and Eremotherium laurillardi and compared the results with a previous investigation of Nothrotherium maquinense and Ahytherium aureum. Differential diagnostic analysis revealed six varieties of musculoskeletal diseases: Calcium Pyrosphosphate Deposition Disease (CPPD), Spondyloarthropathy (SpA), Osteoarthritis (OA), Osteochondritis Dessicans (OD), Schmorl’s Node (SN) and Spondylosis Deformans (SD). We also carried out multivariate statistical analyses on all Pleistocene sloths to verify the similarity between taxa based on diagnosed diseases.     

The evolution of armadillos, anteaters and sloths depicted by nuclear and mitochondrial phylogenies: implications for the status of the enigmatic fossil Eurotamandua

The mammalian order Xenarthra (armadillos, anteaters and sloths) is one of the four major clades of placentals, but it remains poorly studied from the molecular phylogenetics perspective. We present here a study encompassing most of the order's diversity in order to establish xenarthrans' intra-ordinal relationships, discuss the evolution of their morphological characters, search for their extant sister group and specify the timing of their radiation with special emphasis on the status of the controversial fossil Eurotamandua. Sequences of three genes (nuclear exon 28 of the Von Willebrand factor and mitochondrial 12S and 16S rRNAs) are compared for eight of the 13 living genera. Phylogenetic analyses confirm the order's monophyly and that of its three major lineages: armadillos (Cingulata), anteaters (Vermilingua) and sloths ('Tardigrada', renamed in 'Folivora'), and our results strongly support the grouping of hairy xenarthrans (anteaters and sloths) into Pilosa. Within placentals, Afrotheria might be the first lineage to branch off, followed by Xenarthra. The morphological adaptative convergence between New World xenarthrans and Old World pangolins is confirmed. Molecular datings place the early emergence of armadillos around the Cretaceous/Tertiary boundary, followed by the divergence between anteaters and sloths in the Early Eocene era. These Tertiary dates contradict the concept of a very ancient origin of modern xenarthran lineages. They also question the placement of the purported fossil anteater (Eurotamandua) from the Middle Eocene period of Europe with the Vermilingua and instead suggest the independent and convergent evolution of this enigmatic taxon.     

The Forelimb of Early Miocene Sloths (Mammalia, Xenarthra, Folivora): Morphometrics and Functional Implications for Substrate Preferences

Early Miocene sloths are represented by a diversity of forms ranging from 38 to 95?kg. Their forelimb bones differ in shape from those of their closest living relatives (less than 10?kg), Bradypus and Choloepus. Such differences in shape could be related to differences in substrate preference (arboreal, semiarboreal, or ground-dwelling) or substrate use (climbing, digging, etc.). In order to detect putative patterns related to substrate preference, 21 linear measurements were defined and taken on the forelimb bones. The sample was composed of 22 specimens of fossil sloths and 134 specimens of extant mammals (marsupials, xenarthrans, pangolins, rodents, primates, and carnivorans), including arboreal, semiarboreal, and ground-dwelling taxa. Principal Components Analyses were performed on logarithms of original measurements, while functional indexes (Index of Fossorial Ability, Brachial Index, and Distal Epiphyseal Index) were calculated on raw data. The first three PCs accounted for 93.8% of the cumulative variability. PC1 roughly represented size, while positive values of PC2 represented mechanical advantage for features related to digging habits. Fossil sloths were clearly separated from living ones, sharing a common morphospace with anteaters and other good diggers. Conversely, living sloths shared a morphospace with primates. Similar results were obtained for DEI and IFA, with fossil sloths showing similar values to extant digging mammals. These results suggest that fossil sloths have a different functional pattern of forelimb use than that of extant ones, probably more similar to vermilinguas and pangolins, including putative good digging capabilities and/or semiarboreal habits. Substrate use seems to be interfering in the analysis of substrate preference based on forelimb morphology.     

Husbandry of a pink fairy armadillo (Chlamyphorus truncatus): case study of a cryptic and little known species in captivity

Pink fairy armadillos, Chlamyphorus truncatus, are poorly known fossorial mammals that are endemic to central Argentina. These smallest of all extant armadillos are rarely observed in the field and extremely difficult to maintain under captive conditions. This case study describes the husbandry of a male pink fairy armadillo that was maintained in an artificial environment for 8 months. A stable, undisturbed environment consisting of abundant compact sand and hiding places on the surface was the key to its successful maintenance. The artificial diet consisted of a semiliquid mixture of ground cat food, insectivore diet, mashed banana, vitamins, and minerals. Any slight modification to its environment or diet triggered a stress response. Zoo Biol 30:225–231, 2011. © 2010 Wiley‐Liss, Inc.     

The evolution of hyoid apparatus in Xenarthra (Mammalia: Eutheria)

The hyoid apparatus reflects aspects of the form and function of feeding in living and extinct organisms and, despite the availability of information about this structure for Xenarthra, it remains little explored from an evolutionary perspective. Here we compare the morphology of the hyoid apparatus in xenarthrans, describing its general morphology and variation in each major clade and score these variations as phylogenetic characters, which were submitted to ancestral states reconstructions. The general hyoid morphology of Xenarthra consists of a v-bone (basihyal fused with the thyrohyals) and three paired bones (stylohyal, epihyal and ceratohyal), which are unfused in the majority of taxa. The clade-specific morphology observed here, allowed us to obtain additional synapomorphies for all major clades of Xenarthra (Cingulata, Pilosa, Folivora and Vermilingua), for Glyptodontididae, and for Nothrotheriidae. The fusion of hyoid elements are convergentelly achieved among the diphyletic extant tree sloths, some extinct ground sloths and glyptodontids. Despite the heavy influence of adaptive evolution related to feeding habits, the morphology of the hyoid apparatus proved to be a valuable source of phylogenetic information.     

Relief index of second mandibular molars is a correlate of diet among prosimian primates and other euarchontan mammals

This study describes and tests a new method of calculating a shape metric known as the relief index (RFI) on lower second molars of extant euarchontan mammals, including scandentians (treeshrews), dermopterans (flying lemurs), and prosimian primates (strepsirhines and tarsiers). RFI is the ratio of the tooth crown three-dimensional area to two-dimensional planar area. It essentially expresses hypsodonty and complexity of tooth shape. Like other measurements of complexity, RFI ignores taxon-specific features, such as certain cusps and crests, which are usually considered in more traditional studies of tooth function. Traditional statistical analyses of the study sample show that RFI distinguishes taxa with differing amounts of structural carbohydrates in their diets, with frugivore/gramnivores being significantly lower in RFI than omnivores, and insectivores/folivores being significantly higher in RFI than the other two. Information on absolute size, or body mass, is needed to reliably parse out insectivores and folivores; however, if the study sample is limited to Primates, RFI alone distinguishes many folivores (lower) from insectivores (higher). Finally, phylogenetically independent contrasts of RFI and dietary preference are strongly correlated with one another, indicating that variance in RFI is better explained by dietary diversity than phylogenetic affinity in this sample. Because of the accuracy and phylogenetic insensitivity of the RFI among Euarchonta, this method can be applied to fossil primates and stem-primates (plesiadapiforms) and used to elucidate and compare their dietary preferences. Such comparisons are important for developing a more detailed view of primate evolution.     

Differences in Tooth Microwear of Populations of Caribou (<Emphasis Type="Italic">Rangifer tarandus</Emphasis>, Ruminantia,Mammalia) and Implications to Ecology,Migration, Glaciations and Dental Evolution

Tooth microwear was analyzed for a large sample of wild-shot barren-ground caribou (Rangifer tarandus groenlandicus) from the Kaminuriak population of eastern Canada. This sample was compared to the microwear of specimens from three Pleistocene localities in North America (Alaska) and western Europe (Caune de l’Arago in France and Salzgitter in Germany). The results show that the extant samples from eastern Canada have seasonal variation in microwear and presumably in diet. The differences in microwear between the various seasons may reflect a cyclic migration of the population within a year. The extinct population from Alaska has extremely blunt teeth (mesowear), as blunt as those of modern zebras and bison. This observation is corroborated by the lowest number of microwear pits. The findings are untypical, as most typical caribou teeth have sharper apices, and we interpret this as an indication of a local habitat that was different with animals feeding on non-typical vegetation. The combination of Rangifer from Caune de l’Arago and Salzgitter reveals a pattern in microwear variability. The Salzgitter is interglacial and shows a greater diversity of browsing (broad spectrum on average number of pits) than the glacial Caune de l’Arago. The interglacial population from Salzgitter is interesting because it shows several different types of browsing. Collectively all the Rangifer teeth show that diet of a brachydont taxon can vary across most of the dietary morphospace of ungulates as represented by tooth microwear. The three Pleistocene samples exhibit microwear that is different from the extant population in question. This observation implies that the recent diet of Rangifer has changed from the typical caribou diet in the past. This indicates dietary change within a species. This is important because it represents dietary evolution without changes in tooth morphology.