26 research outputs found

    Exceptional skull of huayqueriana (mammalia, litopterna, macraucheniidae) from the late miocene of Argentina: Anatomy, systematics, and peleobiological implications

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    The Huayquerías Formation (Late Miocene, Huayquerian SALMA) is broadly exposed in westcentral Argentina (Mendoza). The target of several major paleontological expeditions in the first half of the 20th century, the Mendozan Huayquerías (badlands) have recently yielded a significant number of new fossil finds. In this contribution we describe a complete skull (IANIGLA-PV 29) and place it systematically as Huayqueriana cf. H. cristata (Rovereto, 1914) (Litopterna, Macraucheniidae). The specimen shares some nonexclusive features with H. cristata (similar size, rostral border of the orbit almost level with distal border of M3, convergence of maxillary bones at the level of the P3/P4 embrasure, flat snout, very protruding orbits, round outline of premaxillary area in palatal view, and small diastemata between I3/C and C/P1). Other differences (e.g., lack of sagittal crest) may or may not represent intraspecific variation. In addition to other features described here, endocast reconstruction utilizing computer tomography (CT) revealed the presence of a derived position of the orbitotemporal canal running below the rhinal fissure along the lateroventral aspect of the piriform lobe. CT scanning also established that the maxillary nerve (CN V2) leaves the skull through the sphenoorbital fissure, as in all other litopterns, a point previously contested for macraucheniids. The angle between the lateral semicircular canal and the plane of the base of the skull is about 26°, indicating that in life the head was oriented much as in modern horses. Depending on the variables used, estimates of the body mass of IANIGLA-PV 29 produced somewhat conflicting results. Our preferred body mass estimate is 250 kg, based on the centroid size of 36 3D cranial landmarks and accompanying low prediction error. The advanced degree of tooth wear in IANIGLA-PV 29 implies that the individual died well into old age. However, a count of cementum lines on the sectioned left M2 is consistent with an age at death of 10 or 11 years, younger than expected given its body mass. This suggests that the animal had a very abrasive diet. Phylogenetic analysis failed to resolve the position of IANIGLA-PV 29 satisfactorily, a result possibly influenced by intraspecific variation. There is no decisive evidence for the proposition that Huayqueriana, or any other litoptern, were foregut fermenters.Fil: Forasiepi, Analia Marta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto Argentino de Nivología, Glaciología y Ciencias Ambientales. Provincia de Mendoza. Instituto Argentino de Nivología, Glaciología y Ciencias Ambientales. Universidad Nacional de Cuyo. Instituto Argentino de Nivología, Glaciología y Ciencias Ambientales; ArgentinaFil: MacPhee, Ross D. E.. American Museum Of Natural History; Estados UnidosFil: Hernández del Pino, Santiago Ezequiel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto Argentino de Nivología, Glaciología y Ciencias Ambientales. Provincia de Mendoza. Instituto Argentino de Nivología, Glaciología y Ciencias Ambientales. Universidad Nacional de Cuyo. Instituto Argentino de Nivología, Glaciología y Ciencias Ambientales; ArgentinaFil: Schmidt, Gabriela Ines. Provincia de Entre Ríos. Centro de Investigaciones Científicas y Transferencia de Tecnología a la Producción. Universidad Autónoma de Entre Ríos. Centro de Investigaciones Científicas y Transferencia de Tecnología a la Producción. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Centro de Investigaciones Científicas y Transferencia de Tecnología a la Producción; ArgentinaFil: Amson, Eli. Universitat Zurich; SuizaFil: Grohé, Camille. American Museum Of Natural History; Estados Unido

    Reappraisal of the tribosphenidan mammals from the Trinity Group (Aptian-Albian) of Texas and Oklahoma

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    The Trinity therians have long been the focus of attempts to reconstruct the evolutionary history of higher mammals, especially in the context of the development of tribospheny. In this paper, we update the taxonomy of the tribosphenidan taxa known from the Trinity Group and establish with more confidence the premolar/molar count in each. Many isolated specimens can be referred to a specific tooth locus. Additional diversity is revealed within the Deltatheroida, with the description of an additional species of Oklatheridium; Pappotherium is here considered a likely metatherian based on the inferred presence of four molars, while Holoclemensia is a basal eutherian (the opposite of some traditional interpretations). The remainder of the genera, Kermackia and Slaughteria, cannot be allied with either of the living groups of tribosphenidan mammals using the available data. We identify strong morphological diversity within this assemblage of stem taxa, including modifications to the traditional tribosphenic occlusal pattern in Kermackia. Mammalian evolution at the base of the tribosphenidan radiation was complex, and this underscores the need for caution when interpreting the morphology and relationships of taxa known by incomplete material

    New data on the dentition of the scincomorphan lizard Polyglyphanodon sternbergi

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    Polyglyphanodon sternbergi Gilmore, 1940 is a large−bodied lizard from the Late Cretaceous of North America distinguished by its transversely oriented, interlocking teeth. Initially the teeth of P. sternbergi were described as smooth and blade−like, but recent discoveries of new specimens from the type locality and re−examination of the original material indicate that the chisel−like teeth of P. sternbergi have small, irregular serrations along the blades. These serrations are similar in size to those found on the teeth of the modern herbivorous lizard Iguana iguana and were likely used in a similar manner to crop vegetation, but was also capable of a degree of oral food processing due to the transverse orientation and interlocking arrangement of the dentition of P. sternbergi. Additionally, the presence of transversely oriented teeth with V−shaped blades in the anterior portion of the tooth row of P. sternbergi represents an additional shared characteristic in tooth structure between P. sternbergi and Dicothodon moorensis, Bicuspidon numerosus, and Peneteius aquilonoius; all transversely−tooth polyglyphandontine lizards from the Cretaceous of North America. It appears that the unique dentitions of Polyglyphanodon sternbergi (large teeth with transverse, serrated blades) and Peneteius aquilonius (small teeth with mammal−like specializations) present by the end of the Cretaceous were derived from a bicuspid, transversely oriented precursor tooth with a V−shaped blade

    Multituberculate mammals from near the Early-Late Cretaceous boundary, Cedar Mountain Formation, Utah

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    Herein we describe the oldest well-sampled multituberculate assemblage from the Cretaceous of North America. The fauna is dated at 98.37 Ma and thus approximates the Albian-Cenomanian (Early-Late Cretaceous) boundary. The multituberculate fauna is diverse. Two of the multituberculates (Janumys erebos gen. et sp. n. and an unidentified taxon) are provisionally placed among 'Plagiaulacida'. Another taxon, Ameribaatar zofiae gen. et sp. n., is of uncertain subordinal affinities. The remaining multituberculates appear to represent the advanced suborder Cimolodonta and fall within the 'Paracimexomys group'. We rediagnose Paracimexomys on the basis of the type species, P. priscus, and refer to other species as cf. Paracimexomys (including cf. P. perplexus sp. n.). A revised diagnosis is also provided for Cenomanian Dakotamys. A previously-described species from the Cedar Mountain Formation is placed in Cedaromys gen. n. as C. bestia, together with C. pawus sp. n. Bryceomys is represented in the fauna by B. intermedius sp. n. Relationships of Paracimexomys-group to later taxa remain obscure. However, Bryceomys and Cedaromys share a number of features with Cimolodontidae. Given these resemblances, together with the fact that Cimolodontidae retain certain plesiomorphies (stout lower incisor, gigantoprismatic enamel) with respect to Ptilodontoidea (to which they are commonly referred), we suggest that Cimolodontidae may have arisen from a clade within the 'Paracimexomys group', independent of ptilodontoids.W pracy opisano najstarszy dobrze opróbowany zespół zębów wieloguzkowców (Multituberculata) z kredy Ameryki Północnej. Fauna formacji Cedar Mountain jest datowana na 98,37 mln lat temu, a więc pochodzi mniej więcej z granicy albu i cenomanu (a więc przełomu wczesnej i późnej kredy). Fauna wieloguzkowców jest zróżnicowana. Dwa z nich (Janumys erebos gen. et sp. n. oraz nieoznaczony takson) tymczasowo zaliczono do ,,Plagiaulacida". Kolejny takson, Ameribaatar zofiae gen. et sp. n., ma niejasną przynależność na szczeblu podrzędu. Wydaje się, że pozostałe wieloguzkowce reprezentują, zaawansowany podrząd Cimolodonta i należałoby je umieścić w ,,grupie Paracimexomys". Diagnoza Paracimexomys została zrewidowana na podstawie gatunku typowego, P. priscus, toteż inne gatunki potraktowano jako cf. Paracimexomys (w tym cf. P. perplexus sp. n.). Zrewidowaną diagnozę uzyskał także cenomański Dakotamys. Opisany juz wcześniej z formacji Cedar Mountain gatunek umieszczony został w nowym rdozaju Cedaromys jako C. bestia, obok C. parvus sp. n. Bryceomys reprezentowany jest w opisywanej faunie przez B. intermedius sp. n. Niejasne pozostają pokrewieństwa między grupą Paracimexomys a późniejszymi taksonami. Bryceomys i Cedaromys mają jednak wiele cech wspólnych z rodziną Cimolodontidae. Ze względu na owe podobieństwa, a także na zachowanie przez Cimolodontidae pewnych plezjomorfii (masywny dolny siekacz, gigantopryzmatczne szkliwo) nieobecnych u Ptilodontoidea (do których się je zwykle zalicza), sugerujemy, ze Cimolodontidae mogły się wyodrębnić z kladu w obrębie ,,grupy Paracimexomys", niezależnie od ptilodontoidów

    Earliest Cretaceous mammals from the western United States

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    Mammalian diversity in North America shifted significantly during the Early Cretaceous, from archaic groups dominant in the well-sampled faunas of the Late Jurassic to advanced forms (including early members of modern clades) by the Albian–Cenomanian. However, the dynamics of this transition are poorly understood, since faunas of earliest Cretaceous age are unknown. Here we describe the first fossil mammals from exposures of the Lakota Formation in the Black Hills of South Dakota, a unit correlated with the upper Berriasian–lower Barremian and positioned stratigraphically between the underlying Morrison Formation and Aptian–Albian units exposed elsewhere in North America. The mammalian fauna from the Lakota Formation is transitional with regard to the North American fossil record, representing a broad spectrum of both Jurassic and Cretaceous lineages: present are “plagiaulacidan” multituberculates allied with Late Jurassic Allodontoidea and Early Cretaceous Plagiaulacoidea; the geologically youngest dryolestoid(s) and “triconodontine” triconodontids (characteristic Late Jurassic taxa from the Morrison Formation); the oldest spalacotheriid “symmetrodont”; the first record of an amphitheriid-like stem zatherian from North America (abundant in the Middle Jurassic–earliest Cretaceous of Europe); and the oldest North American tribosphenic mammal (abundant and diverse on the continent by the end of the Early Cretaceous). Taxa making their first North American appearance in the Lakota Formation (Plagiaulacoidea, including a genus also known from the Purbeck of Britain; Spalacotheriidae, stem Zatheria, Tribosphenida) are also known from the Early Cretaceous of Western Europe, suggesting the possibility that they represent immigrants

    Middle Miocene carnivorans from the Monarch Mill Formation, Nevada

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    The lowest part of the Monarch Mill Formation in the Middlegate basin, west-central Nevada, has yielded a middle Miocene (Barstovian Land Mammal Age) vertebrate assemblage, the Eastgate local fauna. Paleobotanical evidence from nearby, nearly contemporaneous fossil leaf assemblages indicates that the Middle Miocene vegetation in the area was mixed coniferous and hardwood forest and chaparral-sclerophyllous shrubland, and suggests that the area had been uplifted to 2700–2800 m paleoaltitude before dropping later to near its present elevation of 1600 m. Thus, the local fauna provides a rare glimpse at a medium- to high-altitude vertebrate community in the intermountain western interior of North America. The local fauna includes the remains of fish, amphibians, reptiles, birds, and 25 families of mammals. Carnivorans, the focus of this study, include six taxa (three of which are new) belonging to four families. Canidae are represented by the borophagine Tomarctus brevirostris and the canine Leptocyon sp. indet. The earliest record and second North American occurrence of the simocyonine ailurid Actiocyon is represented by A. parverratis sp. nov. Two new mustelids, Brevimalictis chikasha gen. et sp. nov. and Negodiaetictis rugatrulleum gen. et sp. nov., may represent Galictinae but are of uncertain subfamilial and tribal affinity. The fourth family is represented by the felid Pseudaelurus sp. indet. Tomarctus brevirostris is limited biochronologically to the Barstovian land mammal age and thus is consistent with the age indicated by other members of the Eastgate local fauna as well as by indirect tephrochronological dates previously associated with the Monarch Mill Formation. Actiocyon parverratis sp. nov. extends the temporal range of the genus Actiocyon from late Clarendonian back to the Barstovian. The Eastgate local fauna improves our understanding of mammalian successions and evolution, during and subsequent to the Mid-Miocene Climatic Optimum (~14–17 Ma)

    Dentition and relationships of the Jurassic mammal Shuotherium

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    The Middle Jurassic mammal Shuotherium has lower molars that possess a trigonid and talonid, but are unique in having the talonid situated in front of the trigonid, rather than behind it, as in molars of usual tribosphenic pattern. Shuotherium dongi Chow and Rich, 1982 was based on a dentary bearing seven teeth, originally interpreted as three premolars and four molars. Based on comparison with other groups of early mammals, we reinterpret the premolar–molar boundary in the holotype of S. dongi, and propose a dental formula of four (or more) premolars and three molars. The ultimate lower premolar (previously identified as the first molar) has a completely developed trigonid and no talonid or pseudo−talonid. We hypothesize that the mesial cingulid on molars of Australosphenida is a highly plausible structural antecedent to the pseudo−talonid of Shuotherium. This and other shared, derived features support a relationship of Shuotherium and Australosphenida as sister−taxa. We hypothesize that the common ancestor of Shuotherium + Australosphenida had a global distribution no younger than early Middle Jurassic, and that the respective clades diverged prior to full separation of Gondwanan and Laurasian landmasses

    A new genus of eomyid rodent from the Miocene of Nevada

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    The description of a new genus (Apeomyoides) of eomyid rodent from the Miocene of Nevada increases the diversity of known taxa, enhances the geographic range, and extends the biochronology for the Apeomyinae (Eomyidae). Three groups of Eomyidae are known from the fossil record of North America. Of the three groups, Neogene taxa include four genera representing the Eomyinae and two genera representing the Apeomyinae; no genera of the subfamily Yoderimyinae are known from the Neogene of the continent. This diversity represents a significant reduction of eomyid taxa compared to the Paleogene, from which 17 genera of eomyines and three genera of yoderimyines are known. In Eurasia, 11 genera of eomyids occurred during the Neogene, with a few taxa that persisted until about 2 million years before present. At present, there are no known eomyids from the last 4.5 million years of the Neogene in North America. Apeomyoides savagei is referable to the subfamily Apeomyinae based on several key structures of the teeth and mandible. This new eomyid is part of the Eastgate local fauna, collected from volcanic ash deposits of the Monarch Mill Formation, Churchill County, Nevada. Apeomyoides has an occlusal pattern that shares characteristics of apeomyines from both North America (Megapeomys and Arikareeomys) and Eurasia (Apeomys and Megapeomys). The unique occlusal pattern and large size of Apeomyoides demonstrates that not all eomyids from North America were small or that their lineages decreased in size through time. Apeomyoides also may provide evidence, which challenges the hypothesis that eomyids within a single lineage from North America became more lophodont in geologically younger genera

    In quest for a phylogeny of Mesozoic mammals

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    We propose a phylogeny of all major groups of Mesozoic mammals based on phylogenetic analyses of 46 taxa and 275 osteological and dental characters, using parsimony methods (Swofford 2000). Mammalia sensu lato (Mammaliaformes of some authors) are monophyletic. Within mammals, Sinoconodon is the most primitive taxon. Sinoconodon, morganucodontids, docodonts, and Hadrocodium lie outside the mammalian crown group (crown therians + Monotremata) and are, successively, more closely related to the crown group. Within the mammalian crown group, we recognize a fundamental division into australosphenidan (Gondwana) and boreosphenidan (Laurasia) clades, possibly with vicariant geographic distributions during the Jurassic and Early Cretaceous. We provide additional derived characters supporting these two ancient clades, and we present two evolutionary hypotheses as to how the molars of early monotremes could have evolved. We consider two alternative placements of allotherians (haramiyids + multituberculates). The first, supported by strict consensus of most parsimonious trees, suggests that multituberculates (but not other alllotherians) are closely related to a clade including spalacotheriids + crown therians (Trechnotheria as redefined herein). Alternatively, allotherians can be placed outside the mammalian crown group by a constrained search that reflects the traditional emphasis on the uniqueness of the multituberculate dentition. Given our dataset, these alternative topologies differ in tree−length by only ~0.6% of the total tree length; statistical tests show that these positions do not differ significantly from one another. Similarly, there exist two alternative positions of eutriconodonts among Mesozoic mammals, contingent on the placement of other major mammalian clades. Of these, we tentatively favor recognition of a monophyletic Eutriconodonta, nested within the mammalian crown group. We suggest that the “obtuse−angle symmetrodonts” are paraphyletic, and that they lack reliable and unambiguous synapomorphies
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