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现存和化石柯氏喙鲸的进化模式:来自中美洲新近纪的证据

Evolutionary Patterns among Living and Fossil Kogiid Sperm Whales: Evidence from the Neogene of Central America.

作者信息

Velez-Juarbe Jorge, Wood Aaron R, De Gracia Carlos, Hendy Austin J W

机构信息

Department of Mammalogy, Natural History Museum of Los Angeles County, Los Angeles, California, United States of America; John D. Cooper Archaeological and Paleontological Center, Department of Geological Sciences, California State University, Fullerton, California, United States of America.

Department of Geological and Atmospheric Sciences, Iowa State University, Ames, Iowa, United States of America.

出版信息

PLoS One. 2015 Apr 29;10(4):e0123909. doi: 10.1371/journal.pone.0123909. eCollection 2015.

DOI:10.1371/journal.pone.0123909
PMID:25923213
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4414568/
Abstract

Kogiids are known by two living species, the pygmy and dwarf sperm whale (Kogia breviceps and K. sima). Both are relatively rare, and as their names suggest, they are closely related to the sperm whale, all being characterized by the presence of a spermaceti organ. However, this organ is much reduced in kogiids and may have become functionally different. Here we describe a fossil kogiid from the late Miocene of Panama and we explore the evolutionary history of the group with special attention to this evolutionary reduction. The fossil consists of cranial material from the late Tortonian (7.5 Ma) Piña facies of the Chagres Formation in Panama. Detailed comparison with other fossil and extant kogiids and the results of a phylogenetic analysis place the Panamanian kogiid, herein named Nanokogia isthmia gen. et sp. nov., as a taxon most closely related to Praekogia cedrosensis from the Messinian (6 Ma) of Baja California and to Kogia spp. Furthermore our results show that reduction of the spermaceti organ has occurred iteratively in kogiids, once in Thalassocetus antwerpiensis in the early-middle Miocene, and more recently in Kogia spp. Additionally, we estimate the divergence between extant species of Kogia at around the late Pliocene, later than previously predicted by molecular estimates. Finally, comparison of Nanokogia with the coeval Scaphokogia cochlearis from Peru shows that these two species display a greater morphological disparity between them than that observed between the extant members of the group. We hypothesize that this reflects differences in feeding ecologies of the two species, with Nanokogia being more similar to extant Kogia. Nanokogia shows that kogiids have been part of the Neotropical marine mammal communities at least since the late Miocene, and gives us insight into the evolutionary history and origins of one of the rarest groups of living whales.

摘要

小抹香鲸科有两个现存物种,侏儒抹香鲸和小抹香鲸(Kogia breviceps和K. sima)。它们都相对罕见,顾名思义,它们与抹香鲸关系密切,都具有鲸蜡器官。然而,这个器官在小抹香鲸科中已大大缩小,功能可能也有所不同。在此,我们描述了一种来自巴拿马晚中新世的小抹香鲸科化石,并特别关注这种进化退化,探讨了该类群的进化史。该化石由巴拿马查格雷斯组托尔托宁晚期(约750万年前)皮尼亚相的颅骨材料组成。通过与其他化石和现存小抹香鲸科进行详细比较以及系统发育分析的结果,将巴拿马小抹香鲸科,在此命名为窄海小抹香鲸(Nanokogia isthmia gen. et sp. nov.),确定为与来自下加利福尼亚墨西拿期(约600万年前)的雪松前海小抹香鲸(Praekogia cedrosensis)以及小抹香鲸属(Kogia spp.)关系最密切的分类单元。此外,我们的研究结果表明,鲸蜡器官的退化在小抹香鲸科中反复出现,一次发生在中新世早期至中期的安特卫普海鲸(Thalassocetus antwerpiensis),最近一次发生在小抹香鲸属(Kogia spp.)。此外,我们估计现存小抹香鲸属物种之间的分化时间约在上新世晚期,比之前分子估计的时间要晚。最后,将窄海小抹香鲸与同时期来自秘鲁的蜗壳前海小抹香鲸(Scaphokogia cochlearis)进行比较表明,这两个物种之间的形态差异比该类群现存成员之间观察到的差异更大。我们推测,这反映了这两个物种在觅食生态上的差异,窄海小抹香鲸与现存小抹香鲸更为相似。窄海小抹香鲸表明,至少从晚中新世以来,小抹香鲸科就是新热带海洋哺乳动物群落的一部分,并让我们深入了解了现存最稀有鲸类群之一的进化史和起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/41a4e995f106/pone.0123909.g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/2d02ca991f1f/pone.0123909.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/4c3d1985fd3c/pone.0123909.g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/cf6fd0ccff25/pone.0123909.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/43875f8487fc/pone.0123909.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/de48203cf5f7/pone.0123909.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/35c9ff22965d/pone.0123909.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/e917c6d09395/pone.0123909.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/750bdbcdb49a/pone.0123909.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/f3fd2b6b3266/pone.0123909.g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/241549672e83/pone.0123909.g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/41a4e995f106/pone.0123909.g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/2d02ca991f1f/pone.0123909.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/4c3d1985fd3c/pone.0123909.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/4db4125b3093/pone.0123909.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/47947e680c7d/pone.0123909.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/cf6fd0ccff25/pone.0123909.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/43875f8487fc/pone.0123909.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/de48203cf5f7/pone.0123909.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/35c9ff22965d/pone.0123909.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/e917c6d09395/pone.0123909.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/750bdbcdb49a/pone.0123909.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/f3fd2b6b3266/pone.0123909.g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/241549672e83/pone.0123909.g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f23/4414568/41a4e995f106/pone.0123909.g013.jpg

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本文引用的文献

1
Sexual selection targets cetacean pelvic bones.性选择作用于鲸类的骨盆骨。
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2
Repeated mass strandings of Miocene marine mammals from Atacama Region of Chile point to sudden death at sea.智利阿塔卡马地区中新世海洋哺乳动物的多次大规模搁浅表明它们在海上突然死亡。
Proc Biol Sci. 2014 Feb 26;281(1781):20133316. doi: 10.1098/rspb.2013.3316. Print 2014 Apr 22.
3
The giant bite of a new raptorial sperm whale from the Miocene epoch of Peru.秘鲁中新世时期一种新型掠食性抹香鲸的巨大咬痕。
利用目标序列捕获解析鲸目动物的系统发育树。
Syst Biol. 2020 May 1;69(3):479-501. doi: 10.1093/sysbio/syz068.
4
Cetacean Skull Telescoping Brings Evolution of Cranial Sutures into Focus.鲸头骨套叠使颅缝线的进化成为焦点。
Anat Rec (Hoboken). 2019 Jul;302(7):1055-1073. doi: 10.1002/ar.24079. Epub 2019 Mar 8.
5
Albicetus oxymycterus, a New Generic Name and Redescription of a Basal Physeteroid (Mammalia, Cetacea) from the Miocene of California, and the Evolution of Body Size in Sperm Whales.阿尔比西鲸(Albicetus oxymycterus),一个新的属名及对来自加利福尼亚中新世的一种基干抹香鲸类(哺乳动物,鲸目)的重新描述,以及抹香鲸体型的演化
PLoS One. 2015 Dec 9;10(12):e0135551. doi: 10.1371/journal.pone.0135551. eCollection 2015.
6
Isthminia panamensis, a new fossil inioid (Mammalia, Cetacea) from the Chagres Formation of Panama and the evolution of 'river dolphins' in the Americas.巴拿马帕那米因鱼,巴拿马查格雷斯组一新的化石齿鲸类(哺乳纲,鲸目)及美洲“河豚”的演化。
PeerJ. 2015 Sep 1;3:e1227. doi: 10.7717/peerj.1227. eCollection 2015.
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Correction: Evolutionary Patterns among Living and Fossil Kogiid Sperm Whales: Evidence from the Neogene of Central America.更正:现存和化石柯氏喙鲸的进化模式:来自中美洲新近纪的证据。
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Nature. 2010 Jul 1;466(7302):105-8. doi: 10.1038/nature09067.
4
Divergence date estimation and a comprehensive molecular tree of extant cetaceans.现存鲸目动物的分歧时间估计和综合分子系统发育树。
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5
Study of the combined effects of a peracetic acid-based disinfectant and surfactants contained in hospital effluents on Daphnia magna.医院废水中基于过氧乙酸的消毒剂和表面活性剂对大型溞的联合作用研究。
Ecotoxicology. 2007 Apr;16(3):327-40. doi: 10.1007/s10646-007-0136-2. Epub 2007 Mar 14.
6
The face that sank the Essex: potential function of the spermaceti organ in aggression.击沉埃塞克斯号的面孔:鲸蜡器官在攻击行为中的潜在作用。
J Exp Biol. 2002 Jun;205(Pt 12):1755-63. doi: 10.1242/jeb.205.12.1755.
7
Functional morphology and homology in the odontocete nasal complex: implications for sound generation.齿鲸类鼻复合体的功能形态学与同源性:对声音产生的影响
J Morphol. 1996 Jun;228(3):223-85. doi: 10.1002/(SICI)1097-4687(199606)228:3<223::AID-JMOR1>3.0.CO;2-3.