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  1. Denazinemys nodosais a Late Cretaceous representative of the North American turtle clade Baenidae diagnosed, among others, by a shell surface texture consisting of raised welts. We provide a detailed description of a partial skeleton from the late Campanian Kaiparowits Formation of Utah, USA, including bone-by-bone analysis of its cranium based on images obtained using micro-computed tomography. A revised phylogenetic analysis confirms placement ofDenazinemys nodosaclose toEubaena cephalicaandBoremysspp. within the clade Eubaeninae. Comparison with a second skull from the Kaiparowits Formation previously assigned toDenazinemys nodosaquestions its referral to this taxon. An assortment of specimens from the Early to Late Campanian of Mexico and the USA had previously been referred toDenazinemys nodosabased on shell surface texture alone, even though this characteristic is known to occur in other baenids. Our review of all available material concludes thatDenazinemys nodosais currently only known from the Late Campanian of New Mexico and Utah.

     
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    Free, publicly-accessible full text available July 31, 2024
  2. Abstract The labyrinth of the vertebrate inner ear is a sensory system that governs the perception of head rotations. Central hypotheses predict that labyrinth shape and size are related to ecological adaptations, but this is under debate and has rarely been tested outside of mammals. We analyze the evolution of labyrinth morphology and its ecological drivers in living and fossil turtles, an understudied group that underwent multiple locomotory transitions during 230 million years of evolution. We show that turtles have unexpectedly large labyrinths that evolved during the origin of aquatic habits. Turtle labyrinths are relatively larger than those of mammals, and comparable to many birds, undermining the hypothesis that labyrinth size correlates directly with agility across vertebrates. We also find that labyrinth shape variation does not correlate with ecology in turtles, undermining the widespread expectation that reptilian labyrinth shapes convey behavioral signal, and demonstrating the importance of understudied groups, like turtles. 
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  3. Lakotemys australodakotensis is an Early Cretaceous paracryptodire known from two shells and a skull from the Lakota Formation of South Dakota, USA. Along with the Early Cretaceous Arundelemys dardeni and the poorly known Trinitichelys hiatti , Lakotemys australodakotensis is generally retrieved as an early branching baenid, but more insights into the cranial anatomy of these taxa is needed to obtain a better understanding of paracryptodiran diversity and evolution. Here, we describe the skull of Lakotemys australodakotensis using micro-computed tomography to provide the anatomical basis for future phylogenetic analyses that will be needed to investigate more precisely the intrarelationships of Paracryptodira . Preliminary comparisons reveal that the cranial anatomy of Lakotemys australodakotensis is very similar to that of the Aptian-Albian basal baenid Arundelemys dardeni , that both taxa exhibit a remarkable combination of derived characters found in baenodds and characters found in non-baenid paracryptodires, particularly Pleurosternidae , and that Lakotemys australodakotensis is the only known baenid to date to possess a canal for the palatine artery. 
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  4. Arundelemys dardeni is an Early Cretaceous paracryptodire known from a single, incomplete, but generally well-preserved skull. Phylogenetic hypotheses of paracryptodires often find Arundelemys dardeni as an early branching baenid. As such, it has a central role in understanding the early evolution of the successful clade Baenidae, which survived the Cretaceous–Paleogene mass extinction, as well as the diversification of Paracryptodira into its subclades, which recent research suggests to perhaps include helochelydrids, compsemydids, pleurosternids, and baenids. Computer tomography scans of the holotype material that were produced for the initial description of Arundelemeys dardeni reveal several errors in the initial anatomical description of the species, which we correct based on element-by-element segmentation. In addition, we provide entirely novel anatomical information, including descriptions of several previously undescribed cranial bones, the endosseous labyrinth, and the cranial scutes, the latter of which are unknown for most paracryptodires. We provide an interpretation of cranial scutes which homologizes the scutes of Arundelemys dardeni with those of other stem turtles. 
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  5. A new fossil site in a previously unexplored part of western Madagascar (the Beanka Protected Area) has yielded remains of many recently extinct vertebrates, including giant lemurs (Babakotia radofilai, Palaeopropithecus kelyus, Pachylemur sp., and Archaeolemur edwardsi), carnivores (Cryptoprocta spelea), the aardvark-like Plesiorycteropus sp., and giant ground cuckoos (Coua). Many of these represent considerable range extensions. Extant species that were extirpated from the region (e.g., Prolemur simus) are also present. Calibrated radiocarbon ages for 10 bones from extinct primates span the last three millennia. The largely undisturbed taphonomy of bone deposits supports the interpretation that many specimens fell in from a rock ledge above the entrance. Some primates and other mammals may have been prey items of avian predators, but human predation is also evident. Strontium isotope ratios (87Sr/86Sr) suggest that fossils were local to the area. Pottery sherds and bones of extinct and extant vertebrates with cut and chop marks indicate human activity in previous centuries. Scarcity of charcoal and human artifacts suggests only occasional visitation to the site by humans. The fossil assemblage from this site is unusual in that, while it contains many sloth lemurs, it lacks ratites, hippopotami, and crocodiles typical of nearly all other Holocene subfossil sites on Madagascar. 
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