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首页> 外文期刊>Canadian journal of earth sciences >Hinge modifications and musculature of strophomenoid brachiopods: examples across the Ordovician-Silurian boundary, Anticosti Island, Quebec
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Hinge modifications and musculature of strophomenoid brachiopods: examples across the Ordovician-Silurian boundary, Anticosti Island, Quebec

机译:链球菌类腕足动物的铰链修饰和肌肉组织:魁北克安蒂科斯蒂岛奥陶纪-西陆纪界的例子

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摘要

Six modifications to the hinge occur in strophomenoid brachiopods from Anticosti Island: (1) overhanging socket ridges; (2) posterolateral socket ridges along the interarea articulate with grooves on the posterior of teeth; (3) anteromedian dental notches articulate with the crests of socket ridges; (4) dental crenulations on the surfaces of teeth mesh with socket ridges; (5) denticles extend laterally to the cardinal extremities; and (6) the margin of the ventral interarea fits into a long socket along the dorsal interarea forming a lateral tooth. Denticulate hinges and dental notches that typify Silurian and Devonian strophomenids begin in the fauna of the Ellis Bay Formation. Thus the most important interval of strophomenid faunal turnover was at the base of the Gamachian (the base of the Hirnantian) and not at the Ordovician-Silurian boundary. Muscle attachment pads in the delthyrial cavity do not correspond to the positions of either the adductor or diductor muscle scars. Pedicle adjustor muscles in modern brachiopods occupy this position. The round gap between the median fold of the pseudodeltidium and groove on chilidium is proposed as the point of emergence of the pedicle muscle. The tiny foramen, commonly sealed early in growth, is suggested to be part of a neanic water-intake system, active before the growth of the cardinal process in ephebic shells. Once the cardinal process appeared, the foramen was blocked. Recurring types of strophomenid ornamentation, such as posteriorly steepened rugae and checkerboard ornamentation, may have served as a plow to redistribute sediment as the shell was pulled backwards along the pedicle.
机译:对来自Anticosti岛的类兜球类腕足动物的铰链进行了六种修改:(1)悬突的socket突; (2)沿区域间的后外侧牙槽在牙齿的后部有凹槽。 (3)前牙槽口与承窝脊的顶部铰接; (4)牙齿表面的齿状弯曲与窝脊啮合; (5)细齿横向延伸至四肢。 (6)腹侧间缘的边缘沿着背侧间缘插入一个长牙槽,形成侧齿。典型的志留纪和泥盆纪斜齿类动物的齿状铰链和齿状缺口始于埃利斯湾组的动物区系。因此,蛇纹石类动物区系更新的最重要间隔是在Gamachian(Hirnantian的基地)的底部,而不是在Ordovician-Silurian边界。上睑腔中的肌肉附着垫不对应于内收肌或扩张肌疤痕的位置。现代腕足动物的椎弓根调节肌占据了这个位置。假del的中位数褶皱与chi上的凹槽之间的圆形间隙被提议作为椎弓根肌肉的出现点。这些微小的孔通常在生长的早期被密封,被认为是神经吸水系统的一部分,活跃于基贝类的基生过程之前。一旦基本过程出现,孔被阻塞。反复出现的蛇纹石类装饰物(例如向后变陡的皱褶和棋盘状装饰物)可能是犁,用来重新分配沉积物,因为壳体沿蒂向后拉。

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