Cretaceous Period (cretaceous + period)

Distribution by Scientific Domains


Selected Abstracts


The angiosperm radiation revisited, an ecological explanation for Darwin's ,abominable mystery'

ECOLOGY LETTERS, Issue 9 2009
Frank Berendse
Abstract One of the greatest terrestrial radiations is the diversification of the flowering plants (Angiospermae) in the Cretaceous period. Early angiosperms appear to have been limited to disturbed, aquatic or extremely dry sites, suggesting that they were suppressed in most other places by the gymnosperms that still dominated the plant world. However, fossil evidence suggests that by the end of the Cretaceous the angiosperms had spectacularly taken over the dominant position from the gymnosperms around the globe. Here, we suggest an ecological explanation for their escape from their subordinate position relative to gymnosperms and ferns. We propose that angiosperms due to their higher growth rates profit more rapidly from increased nutrient supply than gymnosperms, whereas at the same time angiosperms promote soil nutrient release by producing litter that is more easily decomposed. This positive feedback may have resulted in a runaway process once angiosperms had reached a certain abundance. Evidence for the possibility of such a critical transition to angiosperm dominance comes from recent work on large scale vegetation shifts, linking long-term field observations, large scale experiments and the use of simulation models. [source]


Shallow velocity structure along the Hirapur,Mandla profile using traveltime inversion of wide-angle seismic data, and its tectonic implications

GEOPHYSICAL JOURNAL INTERNATIONAL, Issue 2 2000
Kalachand Sain
In order to investigate the velocity structure, and hence shed light on the related tectonics, across the Narmada,Son lineament, traveltimes of wide-angle seismic data along the 240 km long Hirapur,Mandla profile in central India have been inverted. A blocky, laterally heterogeneous, three-layer velocity model down to a depth of 10 km has been derived. The first layer shows a maximum thickness of the upper Vindhyans (4.5 km s,1,) of about 1.35 km and rests on top of normal crystalline basement, represented by the 5.9 km s,1 velocity layer. The anomalous feature of the study is the absence of normal granitic basement in the great Vindhyan Graben, where lower Vindhyan sediments (5.3 km s,1,) were deposited during the Precambrian on high-velocity (6.3 km s,1,) metamorphic rock. The block beneath the Narmada,Son lineament represents a horst feature in which high-velocity (6.5 km s,1,) lower crustal material has risen to a depth of less than 2 km. South of the lineament, the Deccan Traps were deposited on normal basement during the upper Cretaceous period and attained a maximum thickness of about 800 m. [source]


A giant Upper Jurassic turtle revealed by its trackways

LETHAIA, Issue 4 2003
CHRISTIAN GAILLARD
Exceptional fossilization of large tetrapod swimming traces occurs in the Cerin Lagerstätte (Jura Mountains, France). These trackways are imprinted in Jurassic (Late Kimmeridgian) lagoonal fine-grained limestones and are attributed to giant turtles, which swam with a simultaneous movement of their forelimbs like the modern ones. These turtles swam in very shallow waters close to land, perhaps near a nesting area. As a major consequence, these new ichnologic data place the origin of true large marine turtles during the Jurassic period and not during the Cretaceous period as previously considered on the basis of skeletal remains. [source]


Climate change and grasslands through the ages: an overview

GRASS & FORAGE SCIENCE, Issue 2 2007
L. 't Mannetje
Summary Change from cool to warm temperatures and vice versa have occurred throughout geological time. During the Jurassic and Cretaceous periods (206,65 million years ago, Ma) the climate was more uniformly warm and moist than at present and tropical rainforests were widespread. Grasses evolved during the Jurassic period and they expanded greatly as the climate differentiated with reduced rainfall and temperatures. C4 -grasses probably arose during the Oligocene period (24,35 Ma). During the Miocene period (23·8,5·3 Ma) grasslands expanded into huge areas (e.g. prairies in the USA, steppe in Eurasia, and pampas and llanos in South America). During the Quaternary period (1·8 Ma till now) some twenty-two different ice ages with periodicities of about 100 000 years occurred. Eighteen-thousand years ago, north-western Europe had a polar climate with tundra vegetation and the Mediterranean region was covered by steppe. During that time Amazonia was so dry that it was covered in extensive areas of savanna and the Sahara expanded rapidly. Only in the last 10 000 years has a closed rainforest covered the Amazonian region again. However, 9000 years ago a brief period of global warming caused excessive rains, which caused the sea and river levels to rise in north-western Europe with tremendous loss of life. The present period of extreme dryness in the Sahara only started some 5000 years ago and then the desert expanded rapidly into the Sahel. Before that the Sahara was covered by steppe. Global warming took place between about ad 900 and about ad 1200 or 1300 just before the Little Ice Age (1550,1700 ad). The article concludes with a description of temperature and vegetation changes that are occurring in Europe at present. It is predicted that C4 -grasses, which are already present in southern Europe, will further expand but that, in the short term, land abandonment will have much more deleterious effects than temperature change due to increased wild fires, loss of biodiversity and desertification. [source]


Transformation of the pectoral girdle in the evolutionary origin of frogs: insights from the primitive anuran Discoglossus

JOURNAL OF ANATOMY, Issue 1 2006
Pavla Havelková
Abstract Using cleared-and-stained whole mounts and computer-aided three-dimensional reconstructions made from serial histological sections, we studied the development of the pectoral girdle in Discoglossus pictus, an extant member of an ancient frog lineage, represented for example by Eodiscoglossus from the Middle Jurassic to Early Cretaceous periods in Europe. Basic developmental features were compared with those of extinct Temnospondyli, considered to be the most probable anuran ancestors, and with Triadobatrachus, an early Triassic proanuran. In the endochondral girdle, the separate scapula and coracoid of Discoglossus and other anurans (completed by suprascapular and procoracoid cartilages) evolved from the compact scapulocoracoid of temnospondyls by paedomorphosis. In parallel, the dermal ossifications of the girdle were reduced to a small clavicle and cleithrum. The overall reduction in ossification of the anuran pectoral girdle supports the hypothesis of a paedomorphic origin for Anura. The almost simultaneous appearance of dermal and endochondral ossifications may be explained by the accumulation of developmental events during a short, distinct metamorphosis (which did not occur in neotenic temnospondyls living permanently in water). The sternal elements seem to be neomorphs for the most part, which help to cushion the shock of landing in jumping anurans but which also evolved as functional substitutes (insertion area for the pectoralis muscles) of the temnospondyl interclavicle. [source]