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Extinction and recovery patterns of the vegetation across the Cretaceous–Palaeogene boundary — a tool for unravelling the causes of the end-Permian mass-extinction

机译:白垩纪-古近纪边界上植被的灭绝和恢复模式—揭示二叠纪末次大灭绝原因的工具

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摘要

High-resolution palynofloral signatures through the Cretaceous–Palaeogene boundary succession show several features in common with the Permian–Triassic transition but there are also important differences. Southern Hemisphere Cretaceous–Palaeogene successions, to date studied at high resolution only in New Zealand, reveal a diverse palynoflora abruptly replaced by fungi-dominated assemblages that are in turn succeeded by low diversity suites dominated by fern spores, then gymnosperm- and angiosperm-dominated palynofloras of equivalent diversity to those of the Late Cretaceous. This palynofloral signature is interpreted to represent instantaneous (days to months) destruction of diverse forest communities associated with the Chicxulub impact event. The pattern of palynofloral change suggests wholesale collapse of vascular plant communities and short-term proliferation of saprotrophs followed by relatively rapid successional recovery of pteridophyte and seed–plant communities. The Permian–Triassic transition records global devastation of gymnosperm-dominated forests in a short zone synchronous with one or more peaks of the fungal/algal palynomorph Reduviasporonites. This zone is typically succeeded by assemblages rich in lycophyte spores and/or acritarchs. Higher in the succession, these assemblages give way to diverse palynofloras dominated by new groups of gymnosperms. Although different plant families were involved in the mass-extinctions, the general pattern of extinction and recovery is consistent between both events. The major difference is the longer duration for each phase of the Triassic recovery vegetation compared to that of the Paleocene. The protracted extinction-recovery succession at the Permian–Triassic boundary is incompatible with an instantaneous causal mechanism such as an impact of a celestial body but is consistent with hypotheses invoking extended environmental perturbations through flood-basalt volcanism and release of methane from continental shelf sediments.
机译:白垩纪-古近纪边界演替过程中高分辨率的古植物特征显示出与二叠纪-三叠纪过渡相同的几个特征,但也有重要的区别。迄今为止,仅在新西兰以高分辨率研究的南半球白垩纪-古近纪演替揭示了一种多样的古菌丛,突然被真菌为主的组合所取代,随后又被以蕨类孢子为主的低多样性套件继之以裸子植物和被子植物为主的组合与白垩纪晚期具有同等多样性的古植物。该古植物签名被解释为代表与Chixxulub撞击事件相关的各种森林群落的瞬时(数日至数月)破坏。花粉变化的模式表明维管植物群落的全面崩溃和腐生菌的短期增殖,随后蕨类植物和种子植物群落的恢复相对较快。二叠纪-三叠纪过渡期记录了一个短区,以裸子植物为主导的森林遭到全球破坏,同时真菌/藻类古生物Reduviasporonites的一个或多个峰同步发生。该区域通常由富含莱科植物孢子和/或顶头孢子的组合所继承。这些组合在较高的层次上被新的裸子植物群所取代的多样的无花科植物所取代。尽管大灭绝涉及不同的植物科,但两种事件之间灭绝和恢复的一般模式是一致的。主要区别在于三叠纪恢复植被每个阶段的持续时间都比古新世更长。二叠纪-三叠纪边界的长期灭绝-恢复演替与瞬时因果机制(如天体的撞击)不相容,但与假说通过洪水玄武岩火山作用扩展环境扰动以及从大陆架沉积物中释放甲烷的假设相一致。

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