基于现代和化石证据的早期鸟类饮食及其重建的新框架

C. V. Miller, M. Pittman
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引用次数: 13

摘要

鸟类是地球上最多样化的生物之一,在每个主要的生物群系中都有各种各样的生态位。因此,鸟类对我们理解现代生态系统至关重要。不幸的是,我们对现代生态系统进化史的理解受到现代鸟类多样性起源和生态系统生态学知识空白的阻碍。解决这些缺点的一个关键部分是提高我们对最早的鸟类,即非鸟类鸟(即非冠鸟)的理解,特别是对它们的饮食的理解。非鸟类鸟类的饮食一直是一个有争议的问题,很大程度上是因为用于重建它的模糊定性方法。在这里,我们回顾了确定现代和化石鸟类(即冠鸟)以及非鸟类兽脚亚目动物饮食的方法,并评论了它们在应用于非鸟类鸟类时的实用性。我们利用这一点提出了一套可比较的定量方法来确定化石鸟类的饮食,并在此基础上就我们目前对化石鸟类饮食的了解达成共识。虽然没有一种方法可以精确地预测鸟类的饮食,但每种方法都可以排除某些饮食并缩小饮食的可能性。我们建议结合(i)牙齿微磨损,(ii)基于地标的肌肉重建,(iii)稳定同位素地球化学,(iv)体重估计,(v)传统和/或几何形态计量学分析,(vi)杠杆建模,以及(vii)有限元分析来准确重建化石鸟类的饮食。我们的综述提供了实施每种方法的具体方法,并讨论了未来研究人员应牢记的并发症。我们注意到,目前对牙齿中磨损、颅骨传统形态计量学、几何形态计量学和某些稳定同位素系统的评估形式尚未被证明在识别化石鸟类饮食方面是有效的。在此基础上,我们报告了非鸟类鸟类饮食的现状,这仍然是非常不完整的。由于对始祖鸟的研究缺乏数据和相互矛盾的证据,非鸟类祖先的饮食状况仍然不清楚。在早期的非鸟类pygostylians中,孔子鸟(Confuciusornis)有有限元分析和机械优势证据表明其为食草动物,而Sapeornis只有机械优势证据表明其为花岗岩,这与该分类单元已知的化石摄入物质一致。异鸟胸鸟神鸟具有机械上的优势,且足部形态学证据表明其为食肉动物。在hongshanornithid ornithuromorph Hongshanornis中,只有机械优势的证据表明是花岗岩,但这与该分类群胃石摄食的证据一致。机械优势和摄食的鱼类支持鸣鸟目鸟类的食肉性。由于稳健的饮食分配的稀缺性,没有明确的趋势在非鸟类鸟类饮食进化尚未出现。饮食多样性似乎随着时间的推移而增加,但这是一种保存偏见,与早白垩纪Jehol Lagerstätte的优势数据有关。有了这个新的框架和我们对非鸟类鸟类饮食的现有知识的综合,我们预计饮食知识和进化趋势在未来几年将变得更加清晰,特别是当从其他地点和气候中发现化石时。这将使我们对鸟类在中生代生态系统中所扮演的角色以及如何发展成为现代生态系统中的关键角色有更深入、更有力的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The diet of early birds based on modern and fossil evidence and a new framework for its reconstruction
Birds are some of the most diverse organisms on Earth, with species inhabiting a wide variety of niches across every major biome. As such, birds are vital to our understanding of modern ecosystems. Unfortunately, our understanding of the evolutionary history of modern ecosystems is hampered by knowledge gaps in the origin of modern bird diversity and ecosystem ecology. A crucial part of addressing these shortcomings is improving our understanding of the earliest birds, the non‐avian avialans (i.e. non‐crown birds), particularly of their diet. The diet of non‐avian avialans has been a matter of debate, in large part because of the ambiguous qualitative approaches that have been used to reconstruct it. Here we review methods for determining diet in modern and fossil avians (i.e. crown birds) as well as non‐avian theropods, and comment on their usefulness when applied to non‐avian avialans. We use this to propose a set of comparable, quantitative approaches to ascertain fossil bird diet and on this basis provide a consensus of what we currently know about fossil bird diet. While no single approach can precisely predict diet in birds, each can exclude some diets and narrow the dietary possibilities. We recommend combining (i) dental microwear, (ii) landmark‐based muscular reconstruction, (iii) stable isotope geochemistry, (iv) body mass estimations, (v) traditional and/or geometric morphometric analysis, (vi) lever modelling, and (vii) finite element analysis to reconstruct fossil bird diet accurately. Our review provides specific methodologies to implement each approach and discusses complications future researchers should keep in mind. We note that current forms of assessment of dental mesowear, skull traditional morphometrics, geometric morphometrics, and certain stable isotope systems have yet to be proven effective at discerning fossil bird diet. On this basis we report the current state of knowledge of non‐avian avialan diet which remains very incomplete. The ancestral dietary condition in non‐avian avialans remains unclear due to scarce data and contradictory evidence in Archaeopteryx. Among early non‐avian pygostylians, Confuciusornis has finite element analysis and mechanical advantage evidence pointing to herbivory, whilst Sapeornis only has mechanical advantage evidence indicating granivory, agreeing with fossilised ingested material known for this taxon. The enantiornithine ornithothoracine Shenqiornis has mechanical advantage and pedal morphometric evidence pointing to carnivory. In the hongshanornithid ornithuromorph Hongshanornis only mechanical advantage evidence indicates granivory, but this agrees with evidence of gastrolith ingestion in this taxon. Mechanical advantage and ingested fish support carnivory in the songlingornithid ornithuromorph Yanornis. Due to the sparsity of robust dietary assignments, no clear trends in non‐avian avialan dietary evolution have yet emerged. Dietary diversity seems to increase through time, but this is a preservational bias associated with a predominance of data from the Early Cretaceous Jehol Lagerstätte. With this new framework and our synthesis of the current knowledge of non‐avian avialan diet, we expect dietary knowledge and evolutionary trends to become much clearer in the coming years, especially as fossils from other locations and climates are found. This will allow for a deeper and more robust understanding of the role birds played in Mesozoic ecosystems and how this developed into their pivotal role in modern ecosystems.
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