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A new albanerpetontid, Wesserpeton evansae gen. et sp. nov., from the Early Cretaceous (Barremian) Wessex Formation of the Isle of Wight, southern England, is described. Wesserpeton is established on the basis of a unique combination of primitive and derived characters relating to the frontals and jaws which render it distinct from currently recognized albanerpetontid genera: Albanerpeton (Late Cretaceous to Pliocene of Europe, Early Cretaceous to Paleocene of North America and Late Cretaceous of Asia); Celtedens (Late Jurassic to Early Cretaceous of Europe); and Anoualerpeton (Middle Jurassic of Europe and Early Cretaceous of North Africa). Although Wesserpeton exhibits considerable intraspecific variation in characters pertaining to the jaws and, to a lesser extent, frontals, the new taxon differs from Celtedens in the shape of the internasal process and gross morphology of the frontals in dorsal or ventral view. It differs from Anoualerpeton in the lack of pronounced heterodonty of dentary and maxillary teeth; and in the more medial loca− tion and direction of opening of the suprapalatal pit. The new taxon cannot be referred to Albanerpeton on the basis of the morphology of the frontals. Wesserpeton currently represents the youngest record of Albanerpetontidae in Britain.
Until recently, the only mammal remains to be obtained from the Early Cretaceous (Barremian, Wealden Group) Wessex Formation of the Isle of Wight, southern England were a poorly preserved left m2 and a well preserved left I2 crown representing one or possibly two plagiaulacoid multituberculate species. These were recovered in the early 1970s but despite subsequent efforts by a number of workers to recover additional Mesozoic mammal remains none were forthcoming until comprehensive bulk screening of the Wessex Formation was undertaken in a study commenced in 2002. This study resulted in the recovery of a number of new specimens representing an assemblage of at least six taxa. Among these are a well−preserved plagiaulacoid multituberculate left m1 and a similarly preserved left I3. The former permits diagnosis of a new species of eobaatarid, Eobaatar clemensisp. nov. The previously recovered left m2 is also tentatively assigned to the same taxon. In addition, another left m1, somewhat worn as a result of dietary attrition, was recently obtained by a private collector. This is of very similar morphology to the holotype of E. clemensi but slightly larger. It is undoubtedly referable to the same taxon and provides some insight into intraspecific size, and other minor morphological variations in the teeth of the new species. The I3 may also be referable to the new species, in which case it is the first well preserved I3 of a member of Eobaataridae to be fully described.
A new rhynchonellide brachiopod genus Antulanella is erected based on the examination of the external and internal morphologies and shell microstructure of “Rhynchonella pancici”, a common species in the Barremian shallow−water limestones of the Carpatho−Balkanides of eastern Serbia. The new genus is assigned to the subfamily Viarhynchiinae, family Tetrarhynchiidae. The shell of Antulanella is small to rarely medium−sized, subglobose, subcircular, fully costate, with hypothyrid rimmed foramen. The dorsal euseptoidum is much reduced. The dental plates are thin, ventrally divergent. The hinge plates are straight to ventrally convex. The crura possess widened distal ends, rarely raduliform or canaliform. The shell is composed of two calcitic layers. The secondary layer is fine fibrous, homogeneous built up of predominantly anisometric anvil−like fibres. Although data on the shell microstructure of post−Palaeozoic rhynchonellides are still incomplete, it is possible to distinguish two types of secondary layer: (i) fine fibrous typical of the superfamilies Rhynchonelloidea and Hemithiridoidea and (ii) coarse fibrous typical of the superfamilies Pugnacoidea, Wellerelloidea, and Norelloidea. The new genus Antulanella has a fine fibrous microstructure of the secondary layer, which is consistent with its allocation in the Hemithiridoidea. Antulanella pancici occurs in association with other brachiopods showing strong Peritethyan affinity and close resemblance to the Jura fauna (= Subtethyan fauna).
Ceratosaurian theropods evolved in two bursts, first in the Middle and Late Jurassic and then in the Late Cretaceous, leaving a 20 Myr gap in the Early Cretaceous during which remains are rare. We describe here a new ceratosaurian theropod, Camarillasaurus cirugedae, from fluvial deposits of the Camarillas Formation (lower Barremian, Lower Cretaceous) of Camarillas, Teruel Province, NE Spain. The new theropod is represented by a collection of associated bones, including a tooth, a possible cervical vertebra, two sternal plates, the proximal part of a right tibia, a broken right scapulocoracoid, the incomplete sacrum, five caudal vertebrae, an isolated caudal neural arch, a chevron, an almost complete presacral rib and some fragments of vertebrae, ribs, and other elements. Camarillasaurus is differentiated from other theropods by the extreme depth of the tibia proximal end, and a deep longitudinal groove on the tibia. The new dinosaur is a ceratosaur, phylogenetically close to the base of the clade, and perhaps more derived than the Chinese basal ceratosaur Limusaurus. The new taxon is significant in the evolution of the ceratosaurian dinosaurs, being placed temporally between its more common Jurassic and mid-Upper Cretaceous relatives, and it is one of only a few from Laurasia.
A new acrioceratid ammonite, Dissimilites intermedius sp. nov., from the Barremian (Lower Cretaceous) of the Puez area (Dolomites, northern Italy) is described. Dissimilites intermedius sp. nov. is an intermediate form between D. dissimilis and D. trinodosum. The new species combines the ribbing style of D. dissimilis (bifurcating with intercalating single ribs) with the tuberculation style of D. trinodosum (trituberculation on entire shell). The shallow-helical spire, entirely comprising single ribs intercalated by trituberculated main ribs, is similar to the one of the assumed ancestor Acrioceras, whereas the increasing curvation of the younger forms resembles similar patterns observed in the descendant Toxoceratoides. These characters support the hypothesis of a direct evolutionary lineage from Acrioceras via Dissimilites to Toxoceratoides. D. intermedius sp. nov. ranges from the upper Lower Barremian (Moutoniceras moutonianum Zone) to the lower Upper Barremian (Toxancyloceras vandenheckii Zone). The new species allows to better understand the evolution of the genus Dissimilites. The genus appears within the Nicklesia pulchella Zone represented by D. duboise, which most likely evolved into D. dissimilis. In the Kotetishvilia compressissima Zone, two morphological forms developed: smaller forms very similar to Acrioceras and forms with very long shaft and juvenile spire like in D. intermedius sp. nov. The latter most likely gave rise to D. subalternatus and D. trinodosum in the M. moutonianum Zone, forms which were probably ancestral to the genus Toxoceratoides.
A freshwater turtle from the lithographic limestone of Las Hoyas (Barremian of Cuenca, Spain) is described as a new genus and species of Eucryptodira, Hoyasemys jimenezi. The holotype consists of the skull, lower jaw, carapace, plastron, vertebral column, pectoral and pelvic girdle remains, and foreand hindlimbs. Hoyasemys jimenezi gen. et sp. nov. is characterized by three pairs of blind oblique depressions on the ventral surface of the basisphenoid, and a character combination composed, among others, of the articulation between the fourth and fifth cervical vertebrae through a cotyle in the fourth and a condyle in the fifth, amphicoelous caudal centra, and most digits of manus and pes with three elongated phalanges. This study allows clarification of the systematic position of a species of uncertain affinity often identified as “chelydroid” in appearance. A phylogenetic analysis shows Hoyasemys jimenezi gen. et sp. nov. forms a monophyletic group with Judithemys sukhanovi, Dracochelys bicuspis, Sinemys lens, and Ordosemys leios, collectively the sister group of crown Cryptodira.
A new gobiconodontid from Vallipón (Teruel, Spain) represents the first record of this family in Europe. The site has a diverse fossil assemblage mainly composed of isolated bones and teeth probably accumulated by tidal action and water streams in an ancient beach of upper Barremian, in the transitional marine−continental sediments of the Artoles Formation. The new gobiconodontid consist of an isolated upper molar, smaller in size than that element in other gobiconodontids, with a robust cusp A, characterised by lateral bulges on each mesial and distal flanges of that cusp, and a discontinuous cingulum raised at the lingual side. The occlusal outline is smooth compared with Gobiconodon borissiaki, Gobiconodon hoburensis, or Gobiconodon ostromi. The Gobiconodontidae record is exclusively Laurasiatic. The oldest gobiconodontid fossil remains are Hauterivian; though their probable origin has to be found at the Late Jurassic in Central Asia (as inferred from derived character of the first gobiconodontids as well as phylogenetic relationships). At the end of the Early Cretaceous they expanded throughout Laurasia as indicated by findings in Asia, North America, and Spain. Two dispersion events spread gobiconodontids: to the West (Europe) in the Barremian and to the East (North America) during the Aptian/Albian.
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