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This paper reports the use of FEA (Finite Element Analysis) to model dinosaur tracks. Satisfactory reproductions of sauropod ichnites were simulated using 3D numerical models of the elasto-plastic behaviour of soils. Though the modelling was done of ichnites in situ at the Miraflores I tracksite (Soria, Spain), the methodology could be applied to other tracksites to improve their ichnological interpretation and better understand how the type and state of the trodden sediment at the moment the track is created is a fundamental determinant of the morphology of the ichnite. The results obtained explain why the initial and commonly adopted hypothesis—that soft sediments become progressively more rigid and resistant at depth—is not appropriate at this tracksite. We explain why it is essential to consider a more rigid superficial layer (caused by desiccation) overlying a softer layer that is extruded to form a displacement rim. Adult sauropods left trackways behind them. These tracks could be filled up with water due to phreatic level was close to the ground surface. The simulation provides us with a means to explain the differences between similar tracks (of different depths; with or without displacement rims) in the various stratigraphic layers of the tracksite and to explain why temporary and variable conditions of humidity lead to these differences in the tracks. The simulations also demonstrate that track depth alone is insufficient to differentiate true tracks from undertracks and that other discrimination criteria need to be taken into account. The scarcity of baby sauropod tracks is explained because they are shallow and easily eroded.
The radial trace fossil Dactyloidites peniculus occurs in a deep tier in totally bioturbated shoreface sediments of Pliocene age in the Stirone Valley, N Italy, together with Thalassinoides isp. and Ophiomorpha nodosa. Long, narrow shafts running from centre of the radiating structure and abundant faecal pellets in the radial structure were discovered. The trace maker of D. peniculus, probably a polychaete, deposited the pellets deeply in the sediment, probably for reinforcement of the tubes and a gardening of microbes for feeding. This trace fossil exclusively occurs within a narrow horizon at the top of a shallowing−up section interpreted as a high−stand system tract, below a discontinuity surface capped by finer sediments. D. peniculus was formed in soft sandy sediments under stable conditions related to the latest phases of the highstand system tract. Therefore, it is a candidate for indication of similar environmental situations having a soft sandy, but stable sea floor.
The marine Pliocene at the locality of Nefiach (Roussillon Basin, SE France) includes several shell beds constituted by oysters and scallops that bear a diverse and abundant bioerosion trace fossil assemblage. The most abundant trace fossils are Gnathichnus pentax and Radulichnus inopinatus, produced by the grazing activity of echinoids and polyplacophorans upon algae and other microorganisms coating shell surfaces. Other bioerosion traces include polychaete dwellings (Caulostrepsis taeniola and Maeandropolydora sulcans), sponge boring systems (Entobia isp.), and rare bryozoan borings (Pinaceocladichnus isp.), predation structures (Oichnus simplex and repaired durophagous scars), and foraminiferal fixation pits (Centrichnus cf. eccentricus). The trace fossil assemblage records short−term bioerosion in shellgrounds in a moderate energy setting as evinced by the dominance of epigenic or shallow endogenic structures produced in most cases by “instantaneous” behaviors. The assemblage can be assigned to the Gnathichnus ichnofacies, and it contrasts with that found in Pliocene rocky shores in the same geographic area, which are examples of the Entobia ichnofacies. The Gnathichnusichnofacies is validated as an archetypal one and its recurrency demonstrated since the Jurassic. Entobia and Gnathichnus ichnofacies have to be used in the Mesozoic and Cenozoic as substitutes of the previously existing Trypanites ichnofacies, which is still valid in the Palaeozoic.
The trace fossil Spongeliomorpha iberica locally occurs in the Tortonian (Upper Miocene) marine strata of the Fortuna basin in southeastern Spain, and its excellent preservation state allows a reliable reconstruction of its main morphologic features. The burrow systems are branched (but not anastomosing), and they include numerous, short, blind tunnels. The burrow walls are strongly ornamented with bioglyphs displaying a rhomboidal pattern, consisting mostly of individual “Y”−shaped scratches. Smaller, secondary bioglyphs consist of sets of less incised transverse scratches. These features allow us to assign the ichnospecies to a decapod crustacean, most likely an alpheid or thalassinidean shrimp. The burrow apparently served as a refuge for the inhabitant, which fed upon microorganisms growing on the walls of the burrow by means of scraping the interior surfaces with the maxillipeds or other mouth parts. It is also likely that the shrimp used the multiple blind tunnels to store organic material (probably plant detritus) to be used for later consumption. The crustaceans colonized mud firmgrounds, which were formed by erosion during a rapid sea−level fall. Thus, the burrows occur in direct association with erosional regressive surfaces and therefore are good stratigraphic indicators of abrupt paleoenvironmental change.
Numerous tracks and trackways are preserved in the a cross−strata of the Lower Jurassic Navajo Sandstone of northern Arizona and southern Utah, USA. Tracks and trackways of small theropod dinosaurs are particularly abundant within one 10−m−thick interval. This paper describes a crouching trace from a theropod dinosaur that shows impressions of all four limbs, the ischial callosity, the tail, and tracks leading to and away from the crouching site, and revises the interpretation of a well preserved trackway hitherto referred to the synapsid ichnogenus Brasilichnium and here considered to be from a sauropodomorph dinosaur. It is named Navahopus coyoteensisisp. nov. on the basis of morphological differences from the type ichnospecies N. falcipollex. The ichnofamily Navahopodidae is revised to include Tetrasauropous unguiferus, Navahopus falcipollex, and N. coyoteensis.
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