中国二叠纪—三叠纪陆生植物多样性变化的研究

本文基于华南、华北地区二叠纪—三叠纪陆生植物大化石和孢粉的数据库， 对中国二叠纪—三叠纪陆生植物的多样性变化进行了统计分析研究，并重点探讨了在二叠纪—三叠纪界线（Permian-Triassic Boundary，PTB ）陆生植物是否与同期的海洋动物一样发生了同步的集群灭绝事件。 统计分析表明，华南、华北陆生植物大化石的分异度穿过PTB 均显示了较长时续（约37.8Ma）的下降和残存阶段，而孢粉化石在早三叠世的分异度则是上升的。总体上，陆生植物分异度穿过PTB 的变化较同期的海洋动物平稳缓慢。华南地区陆生植物大化石在晚二叠世末长兴期（Changhsingian）虽然伴随着最高的属灭绝率85.94% 和最低的属新生率28.12%，发生了最大的灭绝事件，但在晚二叠世早期和早三叠世的属的灭绝率也较高，分别为61.02% 和66.67% 。种的灭绝率在晚二叠世早期从早二叠世晚期的39%大幅度上升到80.36%，晚二叠世晚期达峰值97%，早三叠世稍降为93%，显然高于其它时段灭绝率范围（30—70%）。种和属的灭绝率呈现了同样的高峰阶段，从晚二叠世早期至早三叠世，时续为20.8 百万年（Ma）。基于更替率分析，华南地区陆生植物的高更替率事件分别发生在早二叠世晚期（93.75%）、早三叠世（90.92%）和晚三叠世（91.38%），但陆生植物在穿越早二叠世晚期—晚三叠世的整个过程中，更替率波动不大、比较平稳。华北地区陆生植物大化石穿越PTB 的灭绝率比华南地区低，属级高灭绝率事件集中在晚二叠世早期（67.31%）和晚二叠世晚期（63.89%）， 时续为14.8Ma，种级高灭绝率事件与华南地区类似，集中在晚二叠世早期（85.67%）、晚二叠世晚期（90.86%）和早三叠世（80.28% ）三个阶段，时续为20.8Ma 。显而易见，这比同期海洋动物集群灭绝的时续（3—11Ma ）要长。 本文基于这些分析结果，仔细考虑了集群灭绝的4 个特点（即量值、广度、幅度和时续），认为华南、华北陆生植物在PTB 并未发生集群灭绝事件，而是发生了演化替代，即陆生植物穿过PTB 经历了大的植物群重组和新种的演化。总体上，中国二叠纪—三叠纪陆生植物中选择性灭绝非常明显，古生代占优势的种子蕨、真蕨类、木本石松类和楔叶类逐渐被早中生代比较进化的裸子植物和真蕨类植物所替代，陆生植物穿过PTB 显示了危机（灭绝）—残存—复苏—辐射的宏演化式样。

重庆老龙洞二叠系-三叠系界线地层微生物岩研究

The largest mass extinction in the Phanerozoic happened at the end of the Permian. The microbialites formed in the extreme environments after the mass extinction has become a hotspot for geologists and paleontologists throughout the world. The dendroid microbialites that were described for the first time in 1999 from the Permian-Triassic boundary section at Laolongdong, Chongqing, have been studied by many geologists from China and overseas. Two important viewpoints about their origin have been proposed. Some researchers believed that they resemble Quaternary travertine shrubs in form, and may belong to microbialites. Some other researchers proposed that the dendroid structure is composed of clots formed by coccoidal cynaobacteria, and is microbialite. Our detailed survey on the section reveals that: (1) there is an interval of speckled “microbialite” in the section, and it underlies the dendroid “microbialite”, (2) the dendroid “microbialite” does not always have dendroid appearance; they are dendroid only in very local places; they are not dendroid in most places; for this reason, they are not comparable to recent tufa; (3) the volume of the dendroid structure greatly increases toward the top of the dendroid microbialite interval: accounting to 70% of the whole rock in the top part. This distribution pattern implies that the formation of this structure may be related to downward migration of the diagenetic fluid. Examination of thin sections reveals that the dendroid structure or point-like structure in the “microbialite” look as lighter areas in the thin sections and are composed of large blocky clear calcites containing scattered yellow dirty small calcite rhombi and irregular “points” of relict lime mudstone or wackestone or packstone. Their formation is by any one of the following two processes: (1) dissolution → filling of large blocky calcite; (2) dolomitization → dedolomitization → dissolution by meteoric fresh water → filling by large blocky calcites. It has been found that there are at least two sea-level falls during the P-T transition. As the sea level fall, the carbonate deposits came into supratidal environment, and suffered dolomitization caused by evaporative fluid or mixing water of sea water and meteoric water. Since the fluid migrated downward from the top of the deposits and in random pathway, the dolomitization formed dendroid or speckled dolomitic areas. As the deposits came into subaerial environments, the meteoric fresh water migrated along the dendroid or speckled dolomitic area with higher porosity, and dissolution happened, which caused the rock became spongy or alveolate. In later time, after the strata came into phreatic zone, large clear blocky calcites grew in and filled the pores in the spongy areas. The dendroid and speckled structure were formed in this way, rather than composed of clots formed by coccoid cyanobecteria. The microbial fossils in Laolongdong section include two types. The first is the tube-like cyanobecteria in middle Bed 3, which are generally less than 1 mm in length, taper toward one end, and are internally filled by microspars. They are straight or sinuous, with micritic wall 0.005~0.01 mm thick. Since this kind of microbial fossils are abundant in middle Bed 3, this rock belongs to microbialite. The second type occurs in Bed 5 and lower and middle Bed 6. They are irregular globular in shape, generally 0.2 ~ 0.5 mm in size, with several outward progresses, and internally filled by one layer of needle-like calcite cements on the wall and the large blocky calcite in the inner space. According to their shape and preservation way, it is inferred that this kind of fossils were formed from some kind of bacterial colony. The bacterial colony may be cuticle in composition, since it has some hardness as it is indicated by its resistance to deposit loading. These organisms discomposed during diagenetic time, and formed good porosity. In later diagenetic time, these pores were firstly cemented by needle-like calcites and later filled by large blocky calcites. So, the bacterial colony promoted the formation of dendroid and speckled structures. However, they did not always form such structures. On the other hand, even though no bacterial colony or other microbes or any kind of fossils were present, dendroid or speckled structures can form. Bed 4 of Laolongdong section contains abundant gastropods but no microbial fossils, and is not microbialite, even though it is speckled. The top of Bed 6 is dendroid, but contain no microbial fossils, and is not micrbialite.

Geochemistry of rare earth elements in Permian coals from the Huaibei Coalfield；China

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