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Early Cambrian (early + cambrian)
Selected AbstractsA comparative U,Th,Pb (zircon,monazite) and 40Ar,39Ar (muscovite,biotite) study of shear zones in northern Victoria Land (Antarctica): implications for geochronology and localized reworking of the Ross OrogenJOURNAL OF METAMORPHIC GEOLOGY, Issue 6 2007G. DI VINCENZO Abstract Mylonitic granites from two shear zones in northern Victoria Land (Antarctica) were investigated in order to examine the behaviour of the U,Th,Pb system in zircon and monazite and of the 40Ar,39Ar system in micas during ductile deformation. Meso- and micro-structural data indicate that shear zones gently dip to the NE and SW, have an opposite sense of shear (top-to-the-SW and -NE, respectively) and developed under upper greenschist facies conditions. In situ U,Pb dating by laser-ablation inductively coupled plasma-mass spectrometry of zircon areas with well-preserved igneous zoning patterns (c. 490 Ma) confirm that granites were emplaced during the Early Cambrian to Early Ordovician Ross,Delamerian Orogeny. Monazite from the Bier Point Shear Zone (BPSZ) mainly yielded U,Th,Pb ages of c. 440 Ma, in agreement with in-situ Ar laserprobe ages of syn-shear muscovite and with most Ar ages of coexisting biotite. The agreement of ages derived from different decay schemes and from minerals with different crystal-chemical features suggests that isotope transport in the studied sample was mainly controlled by (re)crystallization processes and that the main episode of ductile deformation in the BPSZ occurred at c. 440 Ma. Cathodoluminscence imaging showed that zircon from the BPSZ contains decomposed areas with faint relics of oscillatory zoning. These areas yielded a U,Pb age pattern which mimics that of monazite but is slightly shifted towards older ages, supporting previous studies which suggest that ,ghost' structures may be affected by inheritance. In contrast, secondary structures in zircon from the Mt. Emison Shear Zone (MESZ) predominantly consist of overgrowths or totally recrystallized areas and gave U,Pb ages of c. 450 and 410 Ma. The c. 450-Ma date matches within errors most monazite U,Th,Pb ages and in-situ Ar ages on biotite aligned along the mylonitic foliation. This again suggests that isotope ages from the different minerals are (re)crystallization ages and constrains the time of shearing in the MESZ to the Late Ordovician. Regionally, results indicate that shear zones were active in the Late Ordovician,Early Silurian and that their development was partially synchronous at c. 440 Ma, suggesting that they belong to a shear-zone system formed in response to ,NE,SW-directed shortening. Taking into account the former juxtaposition of northern Victoria Land and SE Australia, we propose that shear zones represent reactivated zones formed in response to stress applied along the new plate margin as a consequence of contractional tectonics associated with the early stages (Benambran Orogeny) of the development of the Late Ordovician,Late Devonian Lachlan Fold Belt. [source] ORDOVICIAN,PERMIAN PALAEOGEOGRAPHY OF CENTRAL EURASIA: DEVELOPMENT OF PALAEOZOIC PETROLEUM-BEARING BASINSJOURNAL OF PETROLEUM GEOLOGY, Issue 3 2003V. A. Bykadorov In this paper, we discuss three petroleum-bearing basins of Palaeozoic age in Central Eurasia,the Precaspian, Tarim and Chu-Sarysu Basins. We make use of recently-published palaeogeographic maps of the Central Eurasian region, six of which are presented here (Late Ordovician, Early-Middle Devonian, Late Devonian, Early Carboniferous, Early Permian and Late Permian). The maps illustrate the development through the Palaeozoic of the Palaeoasian and Palaeotethys Oceans; of the East European, Siberian and Tarim cratons; and of the Kazakhstan and other microcontinental blocks. The Kazakhstan block formed during the Late Ordovician and is a collage of Precambrian and Early Palaeozoic microcontinents and island arcs. It is surrounded by collisional foldbelts (Ob-Zaisan, Ural-Tianshan and Junggar-Balkhash) which formed in the Late Carboniferous , Permian. We believe that the formation of a stable Kazakhstan block is not consistent with the existence of the previously-identified "Kipchak arc" within the Palaeoasian ocean, or (as has previously been proposed) with activity on this arc up to the end of the Palaeozoic. The oil and gas potential of the Precaspian, Tarim and Chu-Sarysu Basins depends to a large extent on their tectonic stability during the Palaeozoic and subsequent time. The Precaspian Basin has been stable since the Cadomian orogeny (Early Cambrian) and is known to have major hydrocarbon potential. The Tarim Basin (NW China) has somewhat lower potential because the margins of the Tarim continental block have been affected by a series of collisional events; that margin with the Palaeotethys Ocean, for example, was active during the Late Palaeozoic. The Chu-Sarysu Basin on the Kazakhstan block is the least stable of the three and contains only minor gas accumulations. [source] The Ordovician Biodiversification: revolution in the oceanic trophic chainLETHAIA, Issue 2 2008THOMAS SERVAIS The Early Palaeozoic phytoplankton (acritarch) radiation paralleled a long-term increase in sea level between the Early Cambrian and the Late Ordovician. In the Late Cambrian, after the SPICE ,13Ccarb excursion, acritarchs underwent a major change in morphological disparity and their taxonomical diversity increased to reach highest values during the Middle Ordovician (Darriwilian). This highest phytoplankton diversity of the Palaeozoic was possibly the result of palaeogeography (greatest continental dispersal) and major orogenic and volcanic activity, which provided maximum ecospace and large amounts of nutrients. With its warm climate and high atmospheric CO2 levels, the Ordovician was similar to the Cretaceous: a period when phytoplankton diversity was at its maximum during the Mesozoic. With increased phytoplankton availability in the Late Cambrian and Ordovician a radiation of zooplanktonic organisms took place at the same time as a major diversification of suspension feeders. In addition, planktotrophy originated in invertebrate larvae during the Late Cambrian,Early Ordovician. These important changes in the trophic chain can be considered as a major palaeoecological revolution (part of the rise of the Palaeozoic Evolutionary Fauna of Sepkoski). There is now sufficient evidence that this trophic chain revolution was related to the diversification of the phytoplankton, of which the organic-walled fraction is partly preserved. [source] Anatomy and lifestyles of Early Cambrian priapulid worms exemplified by Corynetis and Anningvermis from the Maotianshan Shale (SW China)LETHAIA, Issue 1 2004DI-YING HUANG Accurate information on the anatomy and ecology of worms from the Cambrian Lagerstätten of SW China is sparse. The present study of two priapulid worms Anningvermis n. gen. and Corynetis Luo & Hu, 1999 from the Lower Cambrian Maotianshan Shale biota brings new information concerning the anatomical complexity, functional morphology and lifestyles of the Early Cambrian priapulids. Comparisons are made with Recent priapulids from Sweden (live observations, SEM). The cuspidate pharyngeal teeth of Anningvermis (circumoral pentagons) and the most peculiar radiating oral crown of Corynetis added to the very elongate pharynx of these two forms are interpreted as two different types of grasping apparatus possibly involved in the capture of small prey. Corynetis and Anningvermis are two representative examples of the Early Cambrian endobenthic communities largely dominated by priapulid worms (more than ten species in the Maotianshan Shale biota) and to a much lesser extent by brachiopods. Corynetis and Anningvermis were probably active mud-burrowers and predators of small meiobenthic animals. Likewise predator priapulid worms exploited the interface layer between the seawater and bottom sediment, where meiobenthic organisms were abundant and functioned as prey. This implies that complex prey-predator relationship between communities already existed in the Early Cambrian. This study also shows that the circumoral pentagonal teeth and caudal appendage were present in the early stages of the evolutionary history of the group and were important features of the priapulid body plan already in the Early Cambrian. Two new families, one new genus and new species are introduced and described in the appendix. [source] A critical reappraisal of the fossil record of the bilaterian phylaBIOLOGICAL REVIEWS, Issue 2 2000GRAHAM E. BUDD ABSTRACT It has long been assumed that the extant bilaterian phyla generally have their origin in the Cambrian explosion, when they appear in an essentially modern form. Both these assumptions are questionable. A strict application of stem- and crown-group concepts to phyla shows that although the branching points of many clades may have occurred in the Early Cambrian or before, the appearance of the modern body plans was in most cases later: very few bilaterian phyla sensu stricto have demonstrable representatives in the earliest Cambrian. Given that the early branching points of major clades is an inevitable result of the geometry of clade diversification, the alleged phenomenon of phyla appearing early and remaining morphologically static is seen not to require particular explanation. Confusion in the definition of a phylum has thus led to attempts to explain (especially from a developmental perspective) a feature that is partly inevitable, partly illusory. We critically discuss models for Proterozoic diversification based on small body size, limited developmental capacity and poor preservation and cryptic habits, and show that the prospect of lineage diversification occurring early in the Proterozoic can be seen to be unlikely on grounds of both parsimony and functional morphology. Indeed, the combination of the body and trace fossil record demonstrates a progressive diversification through the end of the Proterozoic well into the Cambrian and beyond, a picture consistent with body plans being assembled during this time. Body-plan characters are likely to have been acquired monophyletically in the history of the bilaterians, and a model explaining the diversity in just one of them, the coelom, is presented. This analysis points to the requirement for a careful application of systematic methodology before explanations are sought for alleged patterns of constraint and flexibility. [source] New Bradoriid Arthropods from the Early Cambrian Balang Formation of Eastern Guizhou, South ChinaACTA GEOLOGICA SINICA (ENGLISH EDITION), Issue 1 2010Jin PENG Abstract: The Early Cambrian Balang Formation is comprised of mudrock and shale, which was deposited in a shelf environment in the eastern part of Guizhou, south China. The Balang Fauna, which consists of seven phyla, occurs in the middle and upper parts of the Balang Formation. Arthropods are important constituents of the Balang Fauna and include a great number of trilobites, large bivalved arthropods, and newly-discovered well-preserved bradoriid fossils. The bradoriids present include three genera and four species: Comptaluta inflate (Cheng, 1974) emend Hou et al., 2002; Comptaluta kailiensis sp. nov, and Alutella elongeta sp. nov, Aluta sp. This faunal assemblage in the Balang Formation is distinguished from the Tsunyiella Chang, 1964, Songlinella Yin, 1978 and Kunmingella Hou, 1956 assemblage which occurs in the Niutitang and Mingxinsi formations of the Yangtze Platform in middle region of Guizhou and which is earlier than the Balang Formation in age. However, this assemblage resembles the ComptalutaÖpik, 1968 assemblage from the Early Cambrian Heilinpu Formation in Wuding County, Yuanan Province and from the Ordian Stage of the Cambrian of Australia. The great abundance of ComptalutaÖpik, 1968 and overall taxonomic diversity of the ComptalutaÖpik, 1968 assemblage set it distinctly apart from the Alutella Kobayashi et Kato, 1951 and Aluta Hou, 1956 assemblages of the Balang Formation. Alutella Kobayashi et Kato, 1951 and Aluta Hou, 1956 also occur in the Early Cambrian Niutitang Formation of the Yangtze Platform of Guizhou. Individual Bradoriids from the Balang Formation are characterized by large size (>3 mm). The discovery of new Bradoriid assemblages not only expands the group's geographical range and assemblage affinities, but also indicates that Bradoriids migrated eastward from shallow-water to deeper-water environments during the Early Cambrian, indicating that they were capable of life in deeper-water, and adaptation to a new ecological setting. [source] New Record of Palaeoscolecids from the Early Cambrian of Yunnan, ChinaACTA GEOLOGICA SINICA (ENGLISH EDITION), Issue 2 2008HU Shixue Abstract: A new palaeoscolecid, Guanduscolex minor Hu, Luo et Fu gen. et sp. nov., with preserved soft parts of introvert and intestines comes from the Lower Cambrian Guanshan fauna of Yunnan, South China. Microstructural details of the cuticle revealed by scanning electron microscopy (SEM) show that each annulation bears three rows of plates and each plate bears 9,10 marginal and 4,5 central nodes. This discovery sheds new light on the relationships and evolutionary pathway of the palaeoscolecids and other early priapulids. [source] An evolutionary fast-track to biocalcificationGEOBIOLOGY, Issue 3 2010D. J. JACKSON The ability to construct mineralized shells, spicules, spines and skeletons is thought to be a key factor that fuelled the expansion of multicellular animal life during the early Cambrian. The genes and molecular mechanisms that control the process of biomineralization in disparate phyla are gradually being revealed, and it is broadly recognized that an insoluble matrix of proteins, carbohydrates and other organic molecules are required for the initiation, regulation and inhibition of crystal growth. Here, we show that Astrosclera willeyana, a living representative of the now largely extinct stromatoporid sponges (a polyphyletic grade of poriferan bauplan), has apparently bypassed the requirement to evolve many of these mineral-regulating matrix proteins by using the degraded remains of bacteria to seed CaCO3 crystal growth. Because stromatoporid sponges formed extensive reefs during the Paelozoic and Mesozoic eras (fulfilling the role that stony corals play in modern coral reefs), and fossil evidence suggests that the same process of bacterial skeleton formation occurred in these stromatoporid ancestors, we infer that some ancient reef ecosystems might have been founded on this microbial,metazoan relationship. [source] MACROEVOLUTION AND MACROECOLOGY THROUGH DEEP TIMEPALAEONTOLOGY, Issue 1 2007NICHOLAS J. BUTTERFIELD Abstract:, The fossil record documents two mutually exclusive macroevolutionary modes separated by the transitional Ediacaran Period. Despite the early appearance of crown eukaryotes and an at least partially oxygenated atmosphere, the pre-Ediacaran biosphere was populated almost exclusively by microscopic organisms exhibiting low diversity, no biogeographical partitioning and profound morphological/evolutionary stasis. By contrast, the post-Ediacaran biosphere is characterized by large diverse organisms, bioprovinciality and conspicuously dynamic macroevolution. The difference can be understood in terms of the unique escalatory coevolution accompanying the early Ediacaran introduction of eumetazoans, followed by their early Cambrian (Tommotian) expansion into the pelagic realm. Eumetazoans reinvented the rules of macroecology through their invention of multitrophic food webs, large body size, life-history trade-offs, ecological succession, biogeography, major increases in standing biomass, eukaryote-dominated phytoplankton and the potential for mass extinction. Both the pre-Ediacaran and the post-Ediacaran biospheres were inherently stable, but the former derived from the simplicity of superabundant microbes exposed to essentially static, physical environments, whereas the latter is based on eumetazoan-induced diversity and dynamic, biological environments. The c. 100-myr Ediacaran transition (extending to the base of the Tommotian) can be defined on evolutionary criteria, and might usefully be incorporated into the Phanerozoic. [source] | ||||||||||