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对阿氏翼龙功能形态学与古生态学的重新评估。

A reappraisal of azhdarchid pterosaur functional morphology and paleoecology.

作者信息

Witton Mark P, Naish Darren

机构信息

School of Earth and Environmental Sciences, University of Portsmouth, Portsmouth, United Kingdom.

出版信息

PLoS One. 2008 May 28;3(5):e2271. doi: 10.1371/journal.pone.0002271.

DOI:10.1371/journal.pone.0002271
PMID:18509539
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2386974/
Abstract

Azhdarchid pterosaurs were among the most widespread and successful of pterosaur clades, but their paleoecology remains controversial. Morphological features common to all azhdarchids include a long, shallow rostrum; elongate, cylindrical cervical vertebrae that formed a long and unusually inflexible neck; and proportionally short wings with an abbreviated fourth phalanx. While azhdarchids have been imagined as vulture-like scavengers, sediment probers, swimmers, waders, aerial predators, or stork-like generalists, most recent authors have regarded them as skim-feeders, trawling their lower jaws through water during flight and seizing aquatic prey from the water's surface. Although apparently widely accepted, the skim-feeding model lacks critical support from anatomy and functional morphology. Azhdarchids lack the many cranial specialisations exhibited by extant skim-feeding birds, most notably the laterally compressed lower jaw and shock absorbing apparatus required for this feeding style. Well-preserved azhdarchid skulls are rare, but their rostra and lower jaws appear to have been sub-triangular in cross-section, and thus dissimilar to those of skim-feeders and sediment probers. Taphonomic data indicates that azhdarchids predominately inhabited inland settings, and azhdarchid morphology indicates that they were poorly suited for all proposed lifestyles bar wading and terrestrial foraging. However, azhdarchid footprints show that their feet were relatively small, padded and slender, and thus not well suited for wading. We argue that azhdarchids were stork- or ground hornbill-like generalists, foraging in diverse environments for small animals and carrion. Proficient terrestrial abilities and a relatively inflexible neck are in agreement with this interpretation.

摘要

阿氏翼龙是翼龙类中分布最广、最成功的类群之一,但其古生态学仍存在争议。所有阿氏翼龙共有的形态特征包括一个长而浅的吻部;细长的圆柱形颈椎,形成了一个长且异常僵硬的脖子;以及比例上较短的翅膀,其第四指骨缩短。虽然阿氏翼龙曾被想象为类似秃鹫的食腐动物、沉积物探测者、游泳者、涉禽、空中捕食者或类似鹳的通才,但最近的大多数作者认为它们是掠过式捕食者,在飞行过程中将下颌拖过水面并从水面抓取水生猎物。尽管掠食模型显然已被广泛接受,但它缺乏来自解剖学和功能形态学的关键支持。阿氏翼龙缺乏现存掠过式捕食鸟类所具有的许多颅骨特化特征,最明显的是这种捕食方式所需的侧向压缩的下颌和减震装置。保存完好的阿氏翼龙头骨很少见,但它们的吻部和下颌在横截面看来似乎是亚三角形的,因此与掠过式捕食者和沉积物探测者的不同。埋藏学数据表明,阿氏翼龙主要栖息在内陆环境中,而阿氏翼龙的形态表明,除了涉禽和陆地觅食外,它们不太适合所有提出的生活方式。然而,阿氏翼龙的足迹表明它们的脚相对较小、有肉垫且细长,因此不太适合涉禽生活。我们认为阿氏翼龙是类似鹳或地犀鸟的通才,在不同环境中觅食小动物和腐肉。熟练的陆地能力和相对僵硬的脖子与这种解释相符。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/45cc30bb6c4e/pone.0002271.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/34bab6ef53b2/pone.0002271.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/eff313721b6a/pone.0002271.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/61c13d12af18/pone.0002271.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/671cf29199ef/pone.0002271.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/1998d8822944/pone.0002271.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/5cb0d6813941/pone.0002271.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/92986e959e77/pone.0002271.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/bfc6aa8c3d9a/pone.0002271.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/45cc30bb6c4e/pone.0002271.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/34bab6ef53b2/pone.0002271.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/eff313721b6a/pone.0002271.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/61c13d12af18/pone.0002271.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/671cf29199ef/pone.0002271.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/1998d8822944/pone.0002271.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/5cb0d6813941/pone.0002271.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/92986e959e77/pone.0002271.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/bfc6aa8c3d9a/pone.0002271.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e15/2386974/45cc30bb6c4e/pone.0002271.g009.jpg

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1
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2
Did pterosaurs feed by skimming? Physical modelling and anatomical evaluation of an unusual feeding method.翼龙是通过掠过水面来觅食的吗?一种独特觅食方式的物理建模与解剖学评估。
PLoS Biol. 2007 Aug;5(8):e204. doi: 10.1371/journal.pbio.0050204.
3
High lift function of the pteroid bone and forewing of pterosaurs.翼龙的翼骨和前翼的高升力功能。
一新的无齿翼龙来自早白垩世热河生物群与朝阳翼龙科的讨论。
Sci Rep. 2023 Dec 21;13(1):22642. doi: 10.1038/s41598-023-48076-7.
4
How did extinct giant birds and pterosaurs fly? A comprehensive modeling approach to evaluate soaring performance.已灭绝的巨型鸟类和翼龙是如何飞行的?一种评估翱翔性能的综合建模方法。
PNAS Nexus. 2022 Mar 10;1(1):pgac023. doi: 10.1093/pnasnexus/pgac023. eCollection 2022 Mar.
5
Quadrupedal water launch capability demonstrated in small Late Jurassic pterosaurs.小型晚侏罗世翼龙展示了四足水上起降能力。
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6
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6
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8
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