M. Archer, Olivia Christmas, S. Hand, K. Black, P. Creaser, H. Godthelp, I. Graham, D. Cohen, D. A. Arena, Caitlin Anderson, G. Soares, Naomi Machin, R. Beck, L. A. Wilson, Troy J Myers, A. Gillespie, B. Khoo, K. Travouillon
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Although known only from a lower molar, it exhibits a plethora of carnivorous adaptations including a hypertrophied protoconid, tiny metaconid and a battery of vertical carnassial blades between most of the major cusps, most of which incorporate carnassial notches to immobilise materials being sheared. It is unique among dasyuromorphians in having a massive entoconid that closes the entire lingual side of the talonid. Comparison with previously known thylacinid and dasyurid hypercarnivores suggests its relationships are closer to dasyurids than thylacinids in the main because of the very large entoconid, a cusp that is relatively small to absent in all known thylacinids but commonly small to large in dasyurids. However, the extent of enlargement of the entoconid suggests that it is not closely related to previously known Cenozoic hypercarnivorous dasyurids in the genera Dasyurus, Glaucodon, Sarcophilus or any of the other previously described Cenozoic dasyurids. Although the early late Miocene Ganbulanyi djadjinguli is only known from an upper molar, the reduced area of its protocone suggests a correspondingly reduced rather than hypertrophied entoconid in its as-yet-unknown lower molars. Reconsideration of the structure of the talonid in species of Sarcophilus even suggests that within that Quaternary lineage, the entoconid may have been entirely lost, with the posteriorly displaced metaconid taking its functional place as an occlusal counterpart for the blades of the protocone. The large size of the new species signals the earliest indication within the dasyurid radiation of a late Cenozoic trend towards gigantism that became evident in many lineages of Australian marsupials. While the age is uncertain, on the basis of associated taxa such as species of Ekaltadeta, it is probably either mid or late Miocene in age. Geological features of the deposit suggest it was formed within a pool in a cave environment that periodically underwent desiccation. Some grains suggest an aeolian as well as an alluvial and pluvial origin for the deposit. This may relate to current understanding about environmental change that took place in the region following the mid Miocene climate oscillation.","PeriodicalId":53647,"journal":{"name":"Memoirs of Museum Victoria","volume":"1 1","pages":"137-150"},"PeriodicalIF":0.0000,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"9","resultStr":"{\"title\":\"Earliest known record of a hypercarnivorous dasyurid (Marsupialia), from newly discovered carbonates beyond the Riversleigh world Heritage area, north Queensland\",\"authors\":\"M. Archer, Olivia Christmas, S. Hand, K. Black, P. Creaser, H. Godthelp, I. Graham, D. Cohen, D. A. Arena, Caitlin Anderson, G. Soares, Naomi Machin, R. 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引用次数: 9
摘要
在昆士兰州西北部的里弗斯利世界遗产区西南的一个新的中新生代石灰岩矿床中,发现了一种新的、高度特化的高肉食性大形态动物(Whollydooleya tomnpatrichorum gen. et sp. 11)。牙齿尺寸表明,它的体重可能至少是现存塔斯马尼亚魔鬼(Sarcophilus harrisii)的两倍。虽然只从下臼齿中发现,但它表现出了大量的食肉性适应,包括肥大的原锥体、微小的后锥体和大多数主要尖头之间的一系列垂直肉食叶片,其中大多数都包含肉食切口,以固定被剪切的材料。它的独特之处在于它有一个巨大的内突,封闭了整个舌侧的距骨。与先前已知的袋狼类和袋狼类超食肉动物的比较表明,它与袋狼类的关系比袋狼类更接近,主要是因为它有非常大的内圆锥,一个在所有已知的袋狼类中相对较小或没有的尖,而在袋狼类中通常从小到大。然而,内圆锥的扩大程度表明,它与先前已知的新生代Dasyurus属、Glaucodon属、Sarcophilus属或任何其他先前描述的新生代dasyurids没有密切的关系。虽然晚中新世早期Ganbulanyi djadjinguli仅从上磨牙得知,但其原锥体面积的减少表明其下磨牙的内锥体相应减少,而不是肥大。对Sarcophilus物种的talonid结构的重新考虑甚至表明,在第四纪谱系中,内锥体可能已经完全消失,后移位的后锥体取代了原锥体叶片的功能位置。新物种的巨大体型标志着在新生代晚期的dasyurid辐射中最早的迹象,这种趋势在澳大利亚有袋动物的许多谱系中都很明显。虽然时代不确定,但根据相关分类群,如Ekaltadeta种,其时代可能是中新世中期或晚中新世。该矿床的地质特征表明,它是在一个周期性经历干燥的洞穴环境中的一个水池中形成的。一些颗粒表明,该矿床的成因既可能是风成的,也可能是冲积和洪积的。这可能与目前对中新世中期气候振荡后该地区发生的环境变化的理解有关。
Earliest known record of a hypercarnivorous dasyurid (Marsupialia), from newly discovered carbonates beyond the Riversleigh world Heritage area, north Queensland
Whollydooleya tomnpatrichorum gen. et sp. nov. is a new, highly specialised hypercarnivorous dasyuromorphian from a new mid-Cenozoic limestone deposit southwest of the Riversleigh World Heritage Area in northwestern Queensland. Dental dimensions suggest it may have weighed at least twice as much as the living Tasmanian devil (Sarcophilus harrisii). Although known only from a lower molar, it exhibits a plethora of carnivorous adaptations including a hypertrophied protoconid, tiny metaconid and a battery of vertical carnassial blades between most of the major cusps, most of which incorporate carnassial notches to immobilise materials being sheared. It is unique among dasyuromorphians in having a massive entoconid that closes the entire lingual side of the talonid. Comparison with previously known thylacinid and dasyurid hypercarnivores suggests its relationships are closer to dasyurids than thylacinids in the main because of the very large entoconid, a cusp that is relatively small to absent in all known thylacinids but commonly small to large in dasyurids. However, the extent of enlargement of the entoconid suggests that it is not closely related to previously known Cenozoic hypercarnivorous dasyurids in the genera Dasyurus, Glaucodon, Sarcophilus or any of the other previously described Cenozoic dasyurids. Although the early late Miocene Ganbulanyi djadjinguli is only known from an upper molar, the reduced area of its protocone suggests a correspondingly reduced rather than hypertrophied entoconid in its as-yet-unknown lower molars. Reconsideration of the structure of the talonid in species of Sarcophilus even suggests that within that Quaternary lineage, the entoconid may have been entirely lost, with the posteriorly displaced metaconid taking its functional place as an occlusal counterpart for the blades of the protocone. The large size of the new species signals the earliest indication within the dasyurid radiation of a late Cenozoic trend towards gigantism that became evident in many lineages of Australian marsupials. While the age is uncertain, on the basis of associated taxa such as species of Ekaltadeta, it is probably either mid or late Miocene in age. Geological features of the deposit suggest it was formed within a pool in a cave environment that periodically underwent desiccation. Some grains suggest an aeolian as well as an alluvial and pluvial origin for the deposit. This may relate to current understanding about environmental change that took place in the region following the mid Miocene climate oscillation.