50 research outputs found

    Lomas Las Tetas de Cabra fauna

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    88 p. : ill. (1 col.), maps ; 26 cm.Includes bibliographical references (p. 64-70)."Fossil mammal and other vertebrate remains from the Lomas Las Tetas de Cabra in Baja California Norte, Mexico, provide an opportunity to examine the utility of continental scale geochronologies based on land mammal faunas. Early reports proposed a late Paleocene to early Eocene age for this fauna. Recent fieldwork and considerations of cumulative fossil discoveries strongly indicate that the Baja fauna represents the Wasatchian Land Mammal Age (early Eocene) and is strikingly similar to faunas of this age from the western interior of the United States. Wasatchian-age taxa represented in the Baja assemblage include Hyracotherium, Hyopsodus, Meniscotherium (also possibly from Clarkforkian assemblages), Diacodexis, and Prolimnocyon. Also present in the fauna are excellent specimens of Wyolestes and Esteslestes, a new genus of didelphid marsupial, as well as a badly distorted skull of a pantodont. An early Eocene age assignment is supported by analysis of the marine section adjacent to the Tetas de Cabra sequence. The marine organisms are consistent with a middle Ypresian (early Eocene) age assignment. Paleomagnetic analyses of both the terrestrial and marine sections also corroborate this age assignment. These new results substantiate the validity of the Wasatchian as a discrete temporal interval that can be applied at a continental scale. The Wasatchian thus fulfills the expectations for a mammal-based chronology. Similarities, rather than differences, between the Baja assemblage and other Wasatchian-age faunas is the dominant pattern. A choice among dispersal theories for the sources of Wasatchian mammals is not clearly indicated by the faunal evidence"--P. 3

    Azendohsaurus madagaskarensis.

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    126 pages : illustrations, map ; 26 cm.During the Triassic, archosauromorphs became one of the first groups of diapsid reptiles to diversify in terms of body size and morphological disparity in both terrestrial and marine ecosystems across Pangaea. This seemingly rapid divergence, and the numerous unique body plans stemming from it, concomitantly has confounded reconstructions of archosauromorph relationships. Teasing apart homology from homoplasy of anatomical characters in this broad suite of body types remains an enormous challenge with the current sample of taxa. Here, we present the postcranial anatomy of Azendohsaurus madagaskarensis, an early archosauromorph from ?Middle to Upper Triassic strata of Madagascar. Azendohsaurus madagaskarensis is known from nearly the entire skeleton in an ontogenetically variable sample. The holotype locality consists of a monotypic bone bed; preservation ranges from complete but disarticulated bones to articulated sections of the skeleton. Azendohsaurus madagaskarensis embodies an aberrant constellation of archosauromorph features, including an elongated neck, a short, stocky tail, robust limbs, and unexpectedly short digits terminating in large recurved unguals on the manus and pes. Together with the cranium, the postcrania reveal A. madagaskarensis to be another representative of a growing coterie of highly apomorphic and bizarre Triassic archosauromorphs. At the same time, recovery and description of the full anatomy of A. madagaskarensis helps to identify a monophyletic grouping of specialized taxa that includes the North American Late Triassic-aged archosauromorphs Trilophosaurus, Spinosuchus, and Teraterpeton, Indian Pamelaria, and Moroccan Azendohsaurus laaroussii. Moreover, information derived from the skeleton of A. madagaskarensis solidifies the systematic position of these taxa among other archosauromorphs. Using the most comprehensively sampled phylogenetic analysis of early archosauromorphs, we found the clade encompassing the aforementioned taxa as the nearest outgroup of Prolacerta broomi + Archosauriformes. The newly recognized clade containing Azendohsaurus, Trilophosaurus, Spinosuchus, Pamelaria, and Teraterpeton demonstrates high morphological disparity even within a closely related group of archosauromorphs, underscores the polyphyly of protorosaurs (5 prolacertiforms), and suggests that most major divergences within this group occurred in the Triassic. Furthermore, our results indicate that craniodental character states ascribed to a herbivorous diet were much more pervasive across Triassic Archosauromorpha than previously conjectured

    Hyopsodus (Mammalia) from the Tepee Trail Formation (Eocene), northwestern Wyoming. American Museum novitates ; no. 3007

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    19 p. : ill. ; 26 cm.Includes bibliographical references (p. 18-19

    Morphological diversity in notoungulates

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    26 p. : ill. ; 26 cm.Includes bibliographical references (p. 24-26).Appendicular skeletons of isotemnid notoungulates are described from Cañadón Vaca (Vacan "subage", Casamayoran South American Land Mammal "Age", ?middle to late Eocene). Simpson documented three of these, Thomashuxleya externa, Anisotemnus distentus, and Pleurostylodon similis, some 70 years ago, in fashioning a composite isotemnid skeleton, but he did not emphasize their differences from one another. We note variation, especially in the forelimb, that appears to be functionally significant as well as phylogenetically informative. For example, the downwardly curved olecranon, ventrally concave bowing of the ulnar shaft, and orthogonally directed articulation of the elbow joint suggest an erect forelimb stance in Thomashuxleya externa, whereas the forelimbs of Anisotemnus distentus and Pleurostylodon similis show indications of a crouching posture, including ventrally convex bowing of the ulnar shaft with a slight upward curvature of the olecranon, and an elbow joint in which the antebrachium rotated obliquely relative to the humerus. Articular facets on the proximal carpals suggest that the manus of Anisotemnus was habitually extended, indicating a plantigrade stance of the forelimb. Although none of these three taxa have associated hindfoot material, all known Vacan notoungulate astragali have shallow trochlea, well developed and deep grooves for the flexor hallucis longus, which are separated from the trochlea by a fossa that contains a superior astragalar foramen. An isolated notoungulate pes, not referred to any of the three taxa above, appears to be pentadactyl, having a distinctive, divergent tarsometatarsal joint for its hallux. It also has a shallow trochlea, an astragalar foramen, and a flexor groove, indicating limited rotation of the upper ankle joint. Indeed, a survey of known Casamayoran-aged notoungulate astragali indicates that most taxa had limited mobility at the tibioastragalar joint, in stark contrast to post-Eocene faunas in which nearly all the ungulates had greater rotation of the upper ankle joint and were subcursorial, as evidenced by their longer and deeper trochlear articulation and loss of the astragalar foramen. We suggest that the change from ambulatory- to subcursorial-dominated ungulate faunas across the Eocene-Oliogocene boundary mirrors the changes from brachydont to hypsodont faunas over the same time. Decreased temperatures and rainfall resulting in more open habitats may be related to both morphological evolutionary patterns
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