已灭绝袋鼠股骨的血流量意味着其运动强度高于在世的跳跃大型类动物

IF 1.6 3区 生物学 Q2 ZOOLOGY Journal of Mammalian Evolution Pub Date : 2024-01-19 DOI:10.1007/s10914-023-09701-4
Qiaohui Hu, Roger S. Seymour, Edward P. Snelling, Rod T. Wells
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引用次数: 0

摘要

许多已灭绝的袋鼠的粗壮骨骼和颅后解剖表明,它们的主要运动方式可能是多种多样的运动行为,而不是双足跳跃。本研究通过估算已灭绝袋鼠与在世跳跃物种的股骨血流灌注情况,对这一观点进行了研究。在不保留软组织的情况下,可以根据活体和已灭绝物种股骨柄上营养孔的大小来估算股骨血流量。已灭绝的巨齿兽科(Macropus)、巨齿兽科(Protemnodon)和巨齿兽科(Sthenurus、Simosthenurus 和 Procoptodon)之间的股骨血流率估计值相差不大,但在考虑了体重的影响之后,它们的股骨血流率明显高于在世的跳跃类巨齿兽,这与它们所谓的不同运动方式是一致的。巨型石龙子的股骨比从活体跳跃类巨型动物的数据中推断出来的更为粗壮,这可能是由于体型较大的石龙子需要相对较粗壮的腿骨来支撑较重的体重,尤其是在两足并步时单肢负重的情况下。
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Blood flow rate to the femur of extinct kangaroos implies a higher locomotor intensity compared to living hopping macropods

The stocky skeletons and post-cranial anatomy of many extinct kangaroos indicate that they might have engaged in varied locomotor behaviors, rather than bipedal hopping, as their primary mode of locomotion. This study investigates support for this idea by estimating femoral bone perfusion, which is a correlate of locomotor intensity, in extinct kangaroos compared to living hopping species. Femur blood flow rates can be estimated from the sizes of nutrient foramina on the femur shaft of living and extinct species, without preservation of soft tissue. Estimated femur blood flow rates among the extinct Macropus, Protemnodon and Sthenurinae (Sthenurus, Simosthenurus and Procoptodon) are not significantly different from one another but are significantly greater than in living hopping macropods after accounting for the effect of body mass, consistent with their purportedly different locomotor style. The giant sthenurines have more robust femora than extrapolated from data of living hopping macropods, possibly due to the larger sthenurines requiring relatively stronger leg bones to support their heavier body weights, especially if loaded onto a single limb during bipedal striding.

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来源期刊
CiteScore
4.30
自引率
10.50%
发文量
45
审稿时长
>12 weeks
期刊介绍: Journal of Mammalian Evolution is a multidisciplinary forum devoted to studies on the comparative morphology, molecular biology, paleobiology, genetics, developmental and reproductive biology, biogeography, systematics, ethology and ecology, and population dynamics of mammals and the ways that these diverse data can be analyzed for the reconstruction of mammalian evolution. The journal publishes high-quality peer-reviewed original articles and reviews derived from both laboratory and field studies. The journal serves as an international forum to facilitate communication among researchers in the multiple fields that contribute to our understanding of mammalian evolutionary biology.
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