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观察美国中北部墨西哥湾的大西洋尖吻鲛(Richardson, 1836)的牙齿异形现象,并探讨其对化石记录的影响。

Observations on heterodonty within the dentition of the Atlantic Sharpnose Shark, (Richardson, 1836), from the north-central Gulf of Mexico, USA, with implications on the fossil record.

机构信息

Collections Department, McWane Science Center, Birmingham, Alabama, United States.

School of Biological, Environmental, and Earth Sciences, The University of Southern Mississippi, Hattiesburg, Mississippi, United States.

出版信息

PeerJ. 2023 Apr 12;11:e15142. doi: 10.7717/peerj.15142. eCollection 2023.

DOI:10.7717/peerj.15142
PMID:37070096
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10105564/
Abstract

The Atlantic Sharpnose Shark, (Richardson, 1836), is the most common small coastal requiem shark in the north-central Gulf of Mexico, USA. Despite this fact, little is known about the dental variation within this taxon. To help rectify this shortcoming, we examined 126 male and female jaws sets across all maturity stages to document the various types of heterodonty occurring in the dentition of this taxon. Quantitative data gathered from a subset of our sample allowed for us to place teeth within the dentition of into standardized upper and lower parasymphyseal/symphyseal, anterior lateral, and posterior tooth groups. As with all carcharhinid sharks, the dentition of exhibits monognathic and dignathic heterodonty. We also observed significant ontogenetic heterodonty in the species, as the teeth and dentition progress through five generalized developmental stages as the shark matures. The ontogenetic development of serrations on the teeth appears to be closely related to documented dietary changes as the shark matures. Initial diets are comprised of high percentages of invertebrate prey like shrimp, crabs, and squid, but this transitions through ontogeny to a diet that is more reliant on fishes. We also provide the first documentation of gynandric heterodonty in mature male , with development of these seasonal teeth likely enabling a male to grasp female sharks during copulation. Our analysis revealed a tremendous amount of variation in the dentition of , which has direct implications on the taxonomy of fossil . A comparison of the jaws in our sample to those of the extant species of and the morphologically similar , , and allowed us to formulate a list of generic-level characteristics to assist with the identification of isolated teeth. When applied to the fossil record, it is shown that some species previously assigned to likely belong to one of the other aforementioned genera. The earliest occurrence of unequivocal teeth in the fossil record are those of the Eocene † (Arambourg, 1952), the oldest records of which occur in early Ypresian deposits in Alabama and Mississippi, USA. The early Eocene occurrence of unequivocal fossil teeth in Alabama predates the first occurrence of , , and teeth in the state, supporting published molecular and morphological phylogenies positing a basal position for within the Carcharhinidae.

摘要

大西洋尖鼻鲨(Richardson,1836)是美国中北部墨西哥湾最常见的小型沿海鲭鲨。尽管如此,人们对该分类单元的牙齿变异知之甚少。为了纠正这一不足,我们检查了 126 个雄性和雌性颌骨,涵盖了所有成熟阶段,以记录该分类单元牙齿中发生的各种异形齿现象。从我们样本中的一部分收集的定量数据使我们能够将牙齿放入颌骨中的上和下联合/联合前外侧和后牙组中。与所有角鲨目鲨鱼一样,大西洋尖鼻鲨的牙齿表现出单齿型和双齿型异形齿。我们还观察到该物种存在显著的个体发育异形齿,因为鲨鱼随着成熟而经历五个一般发育阶段。牙齿上锯齿的个体发育似乎与鲨鱼成熟过程中饮食变化密切相关。最初的饮食包括高比例的无脊椎动物猎物,如虾、螃蟹和鱿鱼,但随着个体发育的发展,这种饮食逐渐转变为更依赖鱼类的饮食。我们还首次记录了成熟雄性大西洋尖鼻鲨的雌雄异形齿,这些季节性牙齿的发育可能使雄性鲨鱼在交配时抓住雌性鲨鱼。我们的分析揭示了大西洋尖鼻鲨牙齿的巨大变异,这对化石的分类学有直接影响。我们对样本中的颌骨与现存的 和形态相似的 、 、 和 进行比较,制定了一系列属级特征,以协助鉴定孤立的牙齿。将其应用于化石记录表明,一些以前被分配到 的物种可能属于上述其他属之一。在化石记录中,最早出现的明确的 牙齿是始新世的 †(Arambourg,1952 年),最早的记录出现在美国阿拉巴马州和密西西比州的早伊利诺期沉积物中。在阿拉巴马州,早始新世明确的化石 牙齿的出现早于该州首次出现的 、 、和 牙齿的出现,支持了已发表的分子和形态系统发育,这些研究认为在角鲨科中 处于基础地位。

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Cladistics. 1992 Dec;8(4):295-318. doi: 10.1111/j.1096-0031.1992.tb00073.x.
4
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5
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