来自泽万形成的波斯时期的氨基体环球车,古鲁尔峡谷,喀什米尔
概括
氨形头足动物是关键的关联岩层附近的古生代-中生代边界. 在克什米尔发现了一种末波斯时期的氨基体,Cyclolobus walkeri,有助于理解这一关键的地质过渡.
科学领域:
- 古生物学的古生物学
- 在平流图学上,平流图学是平流图学.
- 地质地质地质地质地质地
背景情况:
- 氨形头足动物是生物分层学中至关重要的索引化石.
- 珀米亚-特里亚斯纪的边界代表了一个主要的大规模灭绝事件.
- 跨越这一边界的层次的准确相关性对于理解古环境变化至关重要.
研究的目的:
- 为了报道发现的Cyclolobus walkeri在Zewan形成.
- 改进克什米尔的珀米亚 - 特里亚斯纪边界的生物层级学相关性.
- 为了解最上层的古世海洋生态系统做出贡献.
主要方法:
- 化石的识别和分类学描述.
- 格鲁尔峡谷部分的平流图分析.
- 基于氨基体组合的生物层状图测年法.
主要成果:
- 鉴定出了诊断的波斯晚期的氨形体Cyclolobus walkeri.
- 该标本在Zewan构造中的Perm-Triassic接触层下20米处被发现.
- 这一发现证实了在这个关键部分存在米纪晚期 (上极古) 氨基体组合的存在.
结论:
- 发现Cyclolobus walkeri强化了其在古生代-中生代边界附近的相关层中的实用性.
- 这种化石为克什米尔地区的最上层珀米亚纪提供了精确的标记.
- 这些发现有助于我们更好地了解在这个关键时间段内氨基体的分布和生物分层学.
相关概念视频
Cycloalkanes
Cycloalkanes are saturated cyclic hydrocarbons with carbon atoms arranged in the form of rings. They have two fewer hydrogen atoms than the corresponding acyclic alkane; therefore, their general formula is CnH2n. The structural formulas of cycloalkanes are simplified using the line-angle representation. The regular polygons are used to represent the cycloalkane rings, with each side representing a carbon-carbon bond.
The IUPAC nomenclature of cycloalkanes follows similar rules that apply to...
The IUPAC nomenclature of cycloalkanes follows similar rules that apply to...
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Cyclohexane does not exist in a planar form due to the high angle and torsional strain it would experience in the planar structure. Instead, it adopts non-planar chair and boat conformations.
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal tetrahedral value,...
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal tetrahedral value,...
Conformations of Cycloalkanes
Adolf von Baeyer attempted to explain the instabilities of small and large cycloalkane rings using the concept of angle strain — the strain caused by the deviation of bond angles from the ideal 109.5° tetrahedral value for sp3 hybridized carbons. However, while cyclopropane and cyclobutane are strained, as expected from their highly compressed bond angles, cyclopentane is more strained than predicted, and cyclohexane is virtually strain-free. Hence, Baeyer’s theory that was based on the...
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