The nothrotheriine sloth from riverbank deposits of the Río Acre region of Peru in western Amazonia was originally assigned to Nothropus priscus Burmeister, 1882. Although relatively complete, with essentially the pes unknown, its description was accompanied only by limited information on its cranial remains. The remains of this sloth, actually of late Miocene age, were extensively prepared. Subsequent analysis indicates that its original assignment is incorrect and that it belongs to a new genus and species, which is distinguished from other nothrotheriines by the following (among other) features: notably domed braincase; depressed, narrow snout; lack of parietal ⁄ alisphenoid contact; ulna with prominently projecting anconeal process; distal position of femoral greater trochanter; medial articular condyle of femur butts against patellar trochlea. Phylogenetic analysis places the new genus and species as sister group to the (Pronothrotherium (Nothrotheriops + Nothrotherium)) clade.
Altiplano bolivien, anatomie, genre nouveau, espèces nouvelles.
RÉSUMÉDeux nouveaux Mylodontinae (Xenarthra, Tardigrada, Mylodontoidea) provenant de l'Altiplano bolivien sont décrits. L'un, Pleuro lestodon dalenzae n. sp., a été découvert à quelques mètres sous un tuf volcanique servant de repère stratigraphique, la Toba 76, daté à 5,4 Ma ; il pourrait être d'âge huayquérien (Miocène supérieur) ou à la limite Huayquérien-Montehermoséen. Simo mylodon uccasamamensis n. gen., n. sp., a été découvert dans plusieurs gisements d'une formation comprenant la Toba 76 à sa base et un tuf volcanique daté à 2,8 Ma à son sommet ; il est d'âge Montehermoséen-Chapadmalaléen (Pliocène inférieur et moyen). L'étude de ces taxons montre que ce sont des Mylodontidae plus proches de Glosso therium, Glosso theridium, Kiyumylodon et Paramylodon que de Lestodon ou Th inobadistes.
The occasion of the Xenarthra Symposium during the ICVM 9 meeting allowed us to reflect on the considerable advances in the knowledge of sloths made by the "Xcommunity" over the past two decades, particularly in such aspects as locomotion, mastication, diet, dental terminology, intraspecific variation, sexual dimorphism, and phylogenetic relationships. These advancements have largely been made possible by the application of cladistic methodology (including DNA analyses) and the discovery of peculiar forms such as Diabolotherium, Thalassocnus, and Pseudoglyptodon in traditionally neglected areas such as the Chilean Andes and the Peruvian Pacific desert coast. Modern tree sloths exhibit an upside-down posture and suspensory locomotion, but the habits of fossil sloths are considerably more diverse and include locomotory modes such as inferred bipedality, quadrupedality, arboreality or semiarboreality, climbing, and an aquatic or semi-aquatic lifestyle in saltwater. Modern tree sloths are generalist browsers, but fossil sloths had browsing, grazing, or mixed feeding dietary habits. Discovery of two important sloth faunas in Brazil (Jacobina) and southern North America (Daytona Beach and Rancho La Brea) have permitted evaluation of the ontogenetic variation in Eremotherium laurillardi and the existence of possible sexual dimorphism in this sloth and in Paramylodon harlani. A new dental terminology applicable to a majority of clades has been developed, facilitating comparisons among taxa. An analysis wherein functional traits were plotted onto a phylogeny of sloths was used to determine patterns of evolutionary change across the clade. These analyses suggest that megatherioid sloths were primitively semiarboreal or possessed climbing adaptations, a feature retained in some members of the family Megalonychidae. Pedolateral stance in the hindfoot is shown to be convergently acquired in Mylodontidae and Megatheria (Nothrotheriidae + Megatheriidae), this feature serving as a synapomorphy of the latter clade. Digging adaptations can only be securely ascribed to scelidotheriine and mylodontine sloths, and the latter are also the only group of grazing sloths, the remainder being general browsers.
The analysis of the hyoid apparatus of fossil xenarthrans provides insight on the form of the tongue and its function in food intake and intraoral processing. The hyoid apparatus of xenarthrans is notable for fusion among its elements. The presence of a V-bone, a complex consisting of fused basihyal and thyrohyal bones, is a consistent and probably synapomorphic feature of xenarthrans. Fusion of other elements is variable in fossil xenarthrans. Most fossil sloths retain independent elements, as in living dasypodids and mammals generally. Among nothrotheriids, the elements are slender and their articular surfaces indicate considerable mobility, and the relatively long and horizontal orientation of the geniohyoid muscle suggests considerable tongue protrusion. Among mylodontines, such as Paramylodon and Glossotherium, the elements indicate relatively mobile articulations, except between the stylo- and epihyals. The relatively posterior placement of the apparatus and the length and alignment of the geniohyoid muscle indicate considerable capacity for tongue protrusion. Scelidotherium, however, had rigidly articulated stylohyal and epihyal, and the apparatus lies farther anteriorly, which together with the elongated, steeply inclined mandibular symphysis, indicates a relatively shorter geniohyoid muscle and thus more limited capacity for tongue protrusion. A similar situation is indicated for Megatherium, casting doubt on the classical reconstruction of this sloth as having a long prehensile tongue. Among cingulates Prozaedyus resembles living dasypodids, indicating considerable tongue protrusion important in food acquisition and intake. More extensive fusion of hyoid elements occurs in the cingulates Glyptodon and Proeutatus, in which the stylohyal and epihyal at least, are fused into a single element termed the sigmohyal. The presence of this element supports recent proposals of a sister-group relationship between glyptodonts and eutatines. The rigidity of the apparatus suggests limited tongue protrusion, but the tongue, in glyptodonts at least, was a powerful structure important for intraoral manipulation of food.
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