996 resultados para Late Devonian


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Mode of access: Internet.

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The ischnacanthid acanthodian Grenfellacanthus zerinae gen. et sp. nov. is described on the basis of two large jaw bones from the Late Devonian (late Famennian) Hunter Formation, near Grenfell, N.S.W. The new species is the youngest known ischnacanthid, and the largest ischnacanthid from Gondwana. As for many ischnacanthids, the structure of the jaws and teeth indicate that Grenfellacanthus was probably an ambush predator.

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Rare earth element and yttrium (REE+Y) concentrations were determined in 49 Late Devonian reefal carbonates from the Lennard Shelf, Canning Basin, Western Australia. Shale-normalized (SN) REE+Y patterns of the Late Devonian samples display features consistent with the geochemistry of well-oxygenated, shallow seawater. A variety of different ancient limestone components, including microbialites, some skeletal carbonates (stromatoporoids), and cements, record seawater-like REE+Y signatures. Contamination associated with phosphate, Fe-oxides and shale was tested quantitatively, and can be discounted as the source of the REE+Y patterns. Co-occurring carbonate components that presumably precipitated from the same seawater have different relative REE concentrations, but consistent REE+Y patterns. Clean Devonian early marine cements (n = 3) display REE+Y signatures most like that of modern open ocean seawater and the highest Y/Ho ratios (e.g., 59) and greatest light REE (LREE) depletion (average Nd-SN/Yb-SN = 0.413, SD = 0.076). However, synsedimentary cements have the lowest REE concentrations (e.g., 405 ppb). Non-contaminated Devonian microbialite samples containing a mixture of the calcimicrobe Renalcis and micritic thrombolite aggregates in early marine cement (n = 11) have the highest relative REE concentrations of tested carbonates (average total REE = 11.3 ppm). Stromatoporoid skeletons, unlike modern corals, algae and molluscs, also contain well-developed, seawater-like REE patterns. Samples from an estuarine fringing reef have very different REE+Y patterns with LREE enrichment (Nd-SN/Yb-SN > 1), possibly reflecting inclusion of estuarine colloidal material that contained preferentially scavenged LREE from a nearby riverine input source. Hence, Devonian limestones provide a proxy for marine REE geochemistry and allow the differentiation of co-occurring water masses on the ancient Lennard Shelf. Although appropriate partition coefficients for quantification of Devonian seawater REE concentrations from out data are unknown, hypothetical Devonian Canning Basin seawater REE patterns were obtained with coefficients derived from modern natural proxies and experimental values. Resulting Devonian seawater patterns are slightly enriched in LREE compared to most modem seawaters and suggest higher overall REE concentrations, but are very similar to seawaters from regions with high terrigenous inputs. Our results suggest that most limestones should record important aspects of the REE geochemistry of the waters in which they precipitated, provided they are relatively free of terrigenous contamination and major diagenetic alteration from fluids with high, non-seawater-like REE contents. Hence, we expect that many other ancient limestones will serve as seawater REE proxies, and thereby provide information on paleoceanography, paleogeography and geochemical evolution of the oceans. Copyright (C) 2004 Elsevier Ltd.

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The discovery of the Woodleigh impact structure, first identified by R. P. lasky, bears a number of parallels with that of the Chlcxulub impact structure of K-T boundary age, underpinning complications inherent in the study of buried impact structures by geophysical techniques and drilling. Questions raised in connection with the diameter of the Woodleigh impact structure reflect uncertainties in criteria used to define original crater sizes in eroded and buried impact structures as well as limits on the geological controls at Woodleigh. The truncation of the regional Ajona - Wandagee gravity ridges by the outer aureole of the Woodleigh structure, a superposed arcuate magnetic anomaly along the eastern part of the structure, seismic-reflection data indicating a central > 37 km-diameter dome, correlation of fault patterns between Woodleigh and less-deeply eroded impact structures (Ries crater, Chesapeake Bay), and morphometric estimates all indicate a final diameter of 120 km. At Woodleigh, pre-hydrothermal shock-induced melting and diaplectic transformations are heavily masked by pervasive alteration of the shocked gneisses to montmorillonite-dominated clays, accounting for the high MgO and low K2O of cryptocrystalline components. The possible contamination of sub-crater levels of the Woodlelgh impact structure by meteoritic components, suggested by high Ni, Co, Cr, Ni/ Co and Ni/Cr ratios, requires further siderophile element analyses of vein materials. Although stratigraphic age constraints on the impact event are broad (post-Middle Devonian to pre-Early Jurassic) high-temperature (200-250 degrees C) pervasive hydrothermal activity dated by K-Ar isotopes of illite - smectite indicates an age of 359 +/- 4 Ma. To date neither Late Devonian crater fill, nor impact ejecta fallout units have been identified, although metallic meteoritic ablation spherules of a similar age have been found in the Conning Basin.

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In this study the conodont multielement apparatus of Late Devonian (Famennian) Icriodus altematus is described which has been reconstructed from clustered group findings and separated elements. This apparatus is markedly different from classical ozarkodinid apparatuses and needs further consideration of its functional morphology. Since bedding plane assemblages of Icriodus altematus are yet unknown, a spatial reconstruction of this apparatus and a feeding mechanism are proposed which are based on the oropharyngal apparatus of recent lampreys. Though the extant representatives of petromyzontoids are not close phylogenetic relatives of extinct conodonts, there exist intriguing analogies concerning the morphology of the tooth types and the presumed spatial distribution within the oral cavity of both taxa.

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Emphanisporites rotatus McGregor emend. McGregor 1973 is a distinctive Devonian spore with a known primary source age range in Australia spanning the upper Givetian to early Frasnian (Middle to Late Devonian). This is the first record of the species from Victoria. It occurs as a reworked element in an Early Permian assemblage belonging to the Granularisporites confluens Zone derived from glacigene diamictite in the Bacchus Marsh area. As the predominant direction of Permian ice movement recorded in the Bacchus Marsh district was south-west to north-east, it is possible that the reworked spores were transported from Antarctica.

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This thesis deals with the stratigraphy and brachiopod systematic palaeontology of the latest Devonian (Famennian) to Early Permian (Kungurian) sedimentary sequences of the Tarim Basin, NW China. Brachiopod faunas of latest Devonian and Carboniferous age have been published or currently in press in the course of the Ph.D candidature and are herein appendixed, while the Early Permian brachiopod faunas are systematically described in this thesis. The described Early Permian brachiopod faunas include 127 species, of which 29 are new and 12 indeterminate, and six new genera (subgenera) are proposed; Tarimella, Bmntonella, Marginifera (Arenaria), Marginifera (Nesiotia), Baliqliqia and Ustritskia. A new integrated brachiopod biostratigraphical zonation scheme is proposed, for the first time, for the latest Devonian-Early Permian sequences of the entire Tarim Basin on the basis of this study as well as previously published information (including the Candidate's own published papers). The scheme consists of twenty three brachiopod acm biozones, most of which replace previously proposed assemblage or assemblage zones. The age and distribution of these brachiopod zones within the Tarim Basin and their relationships with other important fossil groups are discussed. In terms of regional correlations and biostratigraphical affinities, the Late Devonian to Early Carboniferous brachiopod faunas of the Tarim Basin are closest to those from South China, while the Late Carboniferous faunas demonstrate strong similarities to coeval faunas from the Urals, central Asia, North China and South China. During the Asselian-Sakmarian, strong faunal links between the Tarim Basin and those of the Urals persisted, while at the same time links with central Asia, North China and South China weakened. On the other hand, during the Artinskian-Kungurian times, affinities of the Tarim faunas with the Urals/Russian Platform rapidly reduced, when those with peri-Gondwana (South Thailand, northern Tibet) and South China increased. Thirty lithofacies (or microfacies) types of four facies associations are recognised for the Late Devonian to early Permian sediments. Based on detailed lithostratigraphy, biostratigraphy and facies analysis, 23 third-order sequences belonging to four supcrsequences are identified for the Late Devonian to Early Permian successions, from which sea-level fluctuation curves are reconstructed. The sequence stratigraphical analysis reveals that four major regional regressions, each marking a distinct supersequence boundary, can be recognised; they correspond to the end-Serpukhovian, end-Moscovian, late Artinskian and end-Kungurian times, respectively. The development of these sequences is considered to have been formed and regulated by the interplay of both eustasy and tectonism. Using the system tract of a sequence as the mapping time unit, a succession of 47 palaeogeographical maps have been reconstructed through the Late Devonian to Early Permian. These maps reveal that the Tarim Basin was first immersed by southwest-directed (Recent geographical orientation) transgression in the late Famennian after the Caledonian Orogeny. Since then, the basin had maintained its geometry as a large, southwest-mouthed embayment until the late Moscovian when most areas were the uplifted above sea-level. The basin was flooded again in late Asselian-Artinskian times when a new transgression came from a large epicontinental sea lying to its northwest. Thereafter, marine deposition was restricted to local areas (southwestern and northwestern margins until the late Kungurian, while deposition of continental deposits prevailed and continued through the Middle and late Permian into the Triassic.

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Upper Devonian rocks of the Iberian Pyrite Belt (IPB) in southwest Spain, comprising the Phyllite-Quartzite Group (PQ) and the lower part of the overlying Volcano-Sedimentary Complex (VSC), contain a diversity of terrestrial and marine palynomorphs (miospores and organic-walled microphytoplankton, respectively), which constitute the basis of this biostratigraphically oriented research project. Part One of the report has previously detailed the miospore content of the constituent 117 palyniferous samples. In the present paper (i.e., the concluding Part Two), the organic-walled microphytoplankton (acritarchs and prasinophyte phycomata) are systematically described and illustrated, and their occurrence in the study material is fully documented. The acritarchs are represented by 23 species (including one species complex) allocated among 14 genera (one of which, Dupliciradiatum, is newly established), together with a very rare and novel category (informally termed Gen. nov. A). The following new acritarch species are formally instituted: Dupliciradiatum crassum (type species), D. tenue, Histopalla languida, and Winwaloeusia repagulata. Five genera allied with the prasinophycean algae are identified; these accommodate a total of 15 species of which two - Cymatiosphaera tenuimembrana and Maranhites multioculus - are formally proposed as new. In addition, representatives of the prasinophyte genera Leiosphaeridia and Tasmanites are recorded but are not discriminated at species level. The microphytoplankton suite is clearly consonant, from previously published occurrences in other regions, with a Late Devonian dating. However, most of the species are known to be relatively long ranging through (and in some cases beyond) that epoch and hence are not amenable to detailed biozonal subdivision of the IPB succession. Moreover, the distribution of the species therein tends to be erratic in comparison with the more consistently occurring miospores, possibly due to stress factors induced by fluctuating conditions in the IPBs Upper Devonian marine environment. By contrast, the land-derived (miospore) assemblages are readily applicable in a blostratigraphic context: they can be correlated precisely with the Devonian miospore biozonation scheme for Western Europe. In those terms, the sampled PQ strata are assignable to the Diducites versabilis-Grandispora cornuta (VCo) Biozone of late Famennian age; while the samples from the anoxic sequence at the base of the VSC belong to the Retispora lepidophyta-Verrucosisporites nitidus (LN) Biozone (latest Famennian = latest Devonian). The biochronostratigraphic data, in conjunction with the findings from earlier IPB studies, imply two appreciable palynostratigraphic breaks within the PQ. These are representative, respectively, of the lower Frasnian-middle Famennian interval and of part of the Strunian/upper Famennian. Speculation currently remains as to whether the inferred gaps are more apparent than real; i.e., whether one or both represent actual hiatuses in IPB sedimentation or are simply a manifestation of hitherto unsampled and/or non-palyniferous PQ strata.

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木本石松植物在晚古生代植物群中一直引人注目,它们是最早在中、晚泥盆世发展乔木和异孢习性的陆生维管植物谱系之一。在这篇报告中,中国两种晚泥盆世(距今约354-370百万年)的木本石松植物被详细地研究了。这两项研究增进了我们对泥盆纪木本石松植物的进化发育生物学的认识。 作者从中国西北部新疆准噶尔盆地上泥盆统的地层中描述了一个新种新疆鳞孢穗Lepidostrobus xinjiangensis sp.nov.,它为我们研究晚泥盆世石松植物的生殖分化和系统发育关系提供了新的认识。这个孢子叶球不同于任何草本石松植物的生殖器官,而与木本石松植物的生殖器官更为相似,它符合鳞孢穗属Lepidostrobus的鉴别性状。它的每个孢子叶由一个楔形的叶柄和一个三角形的叶片构成。孢子叶水平地着生在穗轴上,呈低角度的螺旋排列。叶柄具有侧翼和一个远轴面的脊,其远端延伸为一个上翻的叶片和一个下翻的踵,形成了一种盾状的外貌。孢子囊呈辐向加长、背腹扁的卵球形,具有顶端的纵向开裂。每个孢子囊基部纵向着生在叶柄的近轴面上。在孢子囊中发现了一个柱状的亚孢原组织垫。一个可能的叶舌出现在叶柄近轴面靠孢子囊远端。这个生殖器官是一个小孢子叶球,含石松孢Lycospora型孢子,具有粒状纹饰和赤道凸缘。基于这个鳞孢穗新种,木本石松植物从泥盆纪到石炭纪以来的生殖分化和演化式样在一个系统发育的框架中被讨论了。作者提出,木本石松植物由两性孢子叶球和单孢子叶球所代表的生殖策略到了晚泥盆世已经发展得相当完备,这暗示着系统发育上生有鳞孢穗孢子叶球的木本石松植物比过去所认为得起源要早。 作者重新调查了一个过去描述于中国湖北晚泥盆世(弗拉斯期)黄家磴组地层中的斜方薄皮木Leptophloeum thombicum的树干,并提出关于这个木本石松植物生长结构的新观点。这个树干保存为压扁的硅化化石,具有不均匀渗矿化的初生维管组织和螺旋排列的斜方形叶座。叶座特征符合晚泥盆世广泛分布的植物斜方薄皮木Leptophloeum rhombicum Dawson的鉴别性状。分类上,斜方薄皮木被归入薄皮木科Leptophloeaceae和广义水韭目Isoetales s.l.。这个树干在不同水平的解剖特征证明,斜方薄皮木的个体发育可能符合一种有限的生长方式。结合过去的资料和当前的生长结构分析,作者提出斜方薄皮木具有假单轴分枝的习性,而不是过去所认为的那样长着等二叉分枝的树冠。作者重新复原了这个植物的总体生长形态,它由一个根座式根状茎、一个主干和侧枝三类主要的生长结构单元构成。当这些结果组合了近期的系统发育工作后,它表明斜方薄皮木已经发育了与一些晚泥盆世法门期和石炭纪木本石松植物相似的生长结构,可能代表了早期水韭目植物祖先的生长结构类型之一。

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在现代的陆地植被当中,石松类为草本植物,在植物界中属于高等植物的低等部分。然而在陆地植物起源和发展演化的早期阶段,石松类是陆地植被的重要成分。石炭纪时期石松类处于最繁盛时期,多生长成为高大乔木,形成森林,是陆地植被的优势类群,也是主要的成煤植物。作为演化历史最长的陆地植物之一,石松类在泥盆纪时期就广泛分布于世界各地,泥盆纪成为石松类演化发展的一个非常重要的时期。研究泥盆纪石松类对认识石松类的起源和发展有重要意义。 本论文是作者在博士期间多个工作之中的两个内容,对采自俄罗斯远东地区的晚泥盆世石松类Haskinsia标本以及采自湖南醴陵的晚泥盆世石松类Lilingostrobus longifolius标本进行了研究。 我们在俄罗斯远东地区的标本中发现了具有三角形叶片的简单叶。泥盆纪石松类Haskinsia属的最典型特征就是其叶由叶柄和三角形或戟形的叶片组成。综合标本的其它特征我们将这些标本归入Haskinsia colophylla这个种中。俄罗斯学者曾在与我们相同的采集地点采集了相似的标本并将其命名为Pseudolepidodendron igrischense,经过仔细对比后我们认为俄罗斯学者的标本也应归并入H. colophylla。同时根据Haskinsia属分布于早泥盆世晚期至晚泥盆世早期的特点,我们对采集地点的地层时代进行了修订,认为其地层时代要比俄罗斯学者认为的晚泥盆世至早石炭世要早。 我们在标本中还首次发现了Haskinsia colophylla这个种的孢子囊。在此之前,Haskinsia 属内的H. colophylla和H. sagittata由于具有相类似的叶而被认为可能是同一个种。由于仅在H. sagittata中发现了孢子囊(椭圆形/卵形)而没有发现H. colophylla的生殖结构,无法确切地区分这两个种。我们在标本中发现了着生于孢子叶腹面的圆形孢子囊。这一发现使我们确认了H. colophylla与H. sagittata的区别,这两个种都是有效种。 我们还对采自湖南醴陵望仙桥水库剖面晚泥盆统岳麓山组地层的部分石松类标本进行了研究。该石松类被命名为Lilingostrobus longifolius。它为木本石松类,茎为二岐分枝,叶在茎上螺旋形排列,叶为长披针形,具有中脉。孢子叶球顶生,呈长锥形,顶端钝圆,孢子叶在孢子叶球上呈紧密的螺旋形排列,每轮约6-8枚。孢子叶分化为孢子叶梗和孢子叶片。孢子叶梗与穗轴近垂直,水平向外延伸后向上弯曲成孢子叶片,叶片至少长45mm,超过孢子叶球长度的一半,孢子叶片与营养叶同型。孢子囊长椭圆形,着生于孢子叶梗的上面。Lilingostrobus longifolius为异型孢子叶球,分为大孢子叶球和小孢子叶球。茎轴具有外始式的初生木质部以及呈放射状的次生木质部。管胞次生壁具有梯纹加厚,加厚的横棒之间有纵向的条状物,即“威廉姆森结构”。Lilingostrobus longifolius具有孢子叶分化明显的孢子叶球因而被归入广义的水韭目。根据其管胞类型和孢子叶球特点,我们认为其可能与Sublepidodendron属亲缘关系较近。 通过对Lilingostrobus longifolius的孢子叶球以及解剖特点的分析,我们认为它代表了晚泥盆世石松类中较为先进的一个类群,这种类群在石炭纪时期得到大规模发展。 结合晚泥盆世其他具有生殖结构的石松类,我们认为晚泥盆世时期石松类的生殖结构类型丰富多样,而且远比中泥盆世石松类生殖结构复杂。这个时期石松类的发展为其在石炭纪的进一步演化奠定了基础。同时,在这个时期石松类植物的叶舌与孢子类型关系中,包括四种类型,即不具叶舌产生单型孢子类型,不具叶舌产生异型孢子类型,具叶舌产生单型孢子类型以及具叶舌产生异型孢子类型。这与现代石松类仅具有两种类型即不具叶舌的类群孢子囊产生同型孢子,而具叶舌的类群孢子囊产生异型孢子有很大的差别。