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ON THE PECULIARITIES OF THE EVOLUTIONARY PROCESS IN SHRIMPS (CRUSTACEA, DECAPODA)

机译:论虾虾进化过程的特性(甲壳树,甲板)

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During the evolution of shrimps, the essential aspects of their organization have remained unchanged. Approximately the same adaptations that have generated a large number of parallelisms within this relatively small group of arthropods have been used in the process of their adaptive evolution. This evolutionary process is a typical telogenesis. The ancient shrimp fauna of both Dendrobranchiata and Pleocyemata could have originated in shallow waters not later than the Jurassic. This is confirmed by the remains of Dendrobranchiata found in the shallow sediments of the Cenomanian (early Upper Cretaceous), and of Pleocyemata as inhabitants of shallow water refugia and representatives of the most primitive caridean shrimp family Procarididae. The latter group is very similar morphologically to fossil shrimps of the Jurassic, for example Udorella agassizi. Later, as a result of adaptive radiations at the generic level, the shrimps occupied both continental slope and pelagic zone. These shallow-water species could have been ousted then by a new shrimp fauna during its colonization of the shelf. The previous shrimp fauna might have shifted to and kind of bordered the continental slope. Some part of the species from various genera could have moved deeper along the slope down to the abyssal zone, while some others might have shifted to occupy the pelagic zone. This seems to have been associated with food resources being limited on the slope in the places with low levels of terrigenous sedimentogenesis. Numerous species seem to have switched from the detrital food chain to the grazing one. That process must have been repeated several times, resulting in the survivor representatives of the most ancient and its next faunas to have occurred at ever greater depths. As it follows, a pulsing type of telogenesis has been characteristic of shrimps. Therefore, the modern shrimp fauna consists of young shelf groups with intensive cladogenesis, as well as of groups that have persisted since the Cretaceous (or even Jurassic), and of remains of earlier faunas that have survived at great depths or shallow-water refugia. This must be considered by researchers who use morphological and molecular methods for studying the phylogenetic relationships within and between the two suborders of Decapoda crustaceans.
机译:在虾的进化过程中,其组织的基本方面保持不变。在这一相对较小的节肢动物类群中,产生大量平行现象的适应过程,与它们的适应进化过程大致相同。这种进化过程是典型的休止期。树状鳃亚目和多胞目的古代虾动物群可能起源于不晚于侏罗纪的浅水区。在赛诺曼阶(早上白垩世)的浅层沉积物中发现的树状鳃纲动物遗骸,以及作为浅水避难所居民和最原始的卡利迪安虾科原虾科代表的多胞藻的遗骸证实了这一点。后者在形态上与侏罗纪的化石虾非常相似,例如乌多雷拉·阿加西。后来,由于一般水平的适应性辐射,虾占据了大陆坡和远洋带。当时,这些浅水物种可能在大陆架殖民期间被一种新的虾群驱逐。以前的虾群可能已经转移到了大陆坡附近。来自不同属的一些物种可能已经沿着斜坡向下移动到深海区,而其他一些物种可能已经转移到深海区。这似乎与陆源沉积作用水平较低的地方,斜坡上的食物资源有限有关。许多物种似乎已经从碎屑食物链转变为放牧食物链。这一过程肯定重复了好几次,导致最古老的动物群及其下一个动物群的幸存者代表出现在更深处。因此,脉冲式休止期是虾的特征。因此,现代虾类动物群包括具有密集分支形成的年轻陆架群,以及自白垩纪(甚至侏罗纪)以来一直存在的群,以及在深海或浅水避难所存活的早期动物群的遗迹。研究人员必须考虑到这一点,他们使用形态学和分子方法来研究十足目甲壳动物两个亚目内部和之间的系统发育关系。

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