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A new archaic baleen whale Toipahautea waitaki (early Late Oligocene New Zealand) and the origins of crown Mysticeti

机译:一种新的古鲸头Toipahautea waitaki(新西兰晚渐新世早期)和冠Mysticeti的起源

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摘要

A new genus and species of extinct baleen whale Toipahautea waitaki (Late Oligocene, New Zealand) is based on a skull and associated bones, from the lower Kokoamu Greensand, about 27.5 Ma (local upper Whaingaroan Stage, early Chattian). The upper jaw includes a thin, elongate and apparently toothless maxilla, with evidence of arterial supply for baleen. Open sutures with the premaxilla suggest a flexible (kinetic) upper jaw. The blowhole is well forward. The mandible is bowed laterally and slightly dorsally; unlike the Eomysticetidae, there are no mandibular alveoli, and the coronoid process is tapered and curved laterally. Jaw structure is consistent with baleen-assisted gulp-feeding. The age of early Chattian makes Toipahautea a very early, if not the oldest named, toothless and baleen-bearing mysticete, suggesting that the full transition from toothed to baleen-bearing probably occurred in the Early Oligocene. Late Oligocene mysticetes vary considerably in jaw form and kinesis, tooth form and function, and development of baleen, implying a wide range of raptorial, suctorial and filter-feeding behaviour. More study may elucidate the function of jaws, teeth and baleen in terms of opportunist/generalist feeding, as in modern gray whales, versus specialized feeding. We here propose that early mysticetes, when transitioned from toothed to baleen-bearing, were generalists and opportunists instead of specializing in any forms of feeding strategies. In addition, two different phylogenetic analyses placed Toipahautea either in a polytomy including crown Mysticeti, or immediately basal to the crown, and above †Eomysticetidae in both cases. Because the Toipahautea waitaki holotype is an immature individual, it may plot more basally in phylogeny than its true position.
机译:濒临灭绝的须鲸的新属和种 Toipahautea waitaki(新西兰晚渐新世)是基于头骨和相关骨骼的,来自Kokoamu Greensand下游,约27.5 Ma(Whaingaroan阶段,早期的查天)。上颌骨包括一个细长的细长上颌无牙的上颌骨,有动脉供血。上颌前突的开放缝合线表明上颌有弹性(运动)。气孔正向前方。下颌骨向侧面和背面稍微弯曲。与Eomysticetidae不同,没有下颌肺泡,冠状突呈锥形并横向弯曲。颚的结构与巴利恩辅助的大口喂食一致。查图斯早期的年龄使Toipahautea成为非常早期的(即使不是最古老的)无齿,有须长牙的神秘者,这表明渐新世可能是从有齿到有须长牙的完全过渡。渐新世晚期的神秘菌在下颚形态和运动学,牙齿形态和功能以及软膏的发育方面有很大的不同,这意味着各种各样的猛禽,吸血和取食过滤的行为。像现代灰鲸一样,更多的研究可能阐明机会主义者/全科医生喂养的颌骨,牙齿和巴里翁的功能,而不是专门的喂养。我们在这里提出,早期的神秘主义者,从有齿动物过渡到有熊的动物,是通才和机会主义者,而不是专门从事任何形式的喂养策略。此外,两种不同的系统发育分析将Toipahautea放置在包括冠Mysticeti的多层切开术中,或直接位于冠的基部,并且在两种情况下都位于†Eomysticetidae之上。因为 Toipahautea waitaki整体型是一个不成熟的个体,所以在系统发育上可能比其真实位置更基础地绘图。

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