Seibold I, Helbig A J
Institute of Zoology, University of Greifswald, Kloster, Germany.
Philos Trans R Soc Lond B Biol Sci. 1995 Nov 29;350(1332):163-78. doi: 10.1098/rstb.1995.0150.
The phylogeny of 11 species of Old World vultures (Aves: Accipitriformes, Aegypiinae), three species of New World vultures (Cathartidae) and theri nearest relatives within and outside the order Accipitriformes was investigated based on 1026 nucleotides of the mitochondrial cytochrome b gene. The data support the contention that New World vultures are not birds of prey, but phylogenetic information was insufficient to identify whether they are closer to storks (Ciconiidae) or to Accipitriformes. Four species of Gyps are all closely related and probably speciated within the Pleistocene. Molecular data do not support the split of 'white-backed' vultures from Gyps in a separate genus Pseudogyps. The monotypic genera of large, heavy-billed vultures, Aegypius, Torgos, Trigonoceps and Sarcogyps, are of monophyletic origin. We propose to merge Torgos with Aegypius, but retain Trigonoceps and Sarcogyps as separate genera, Sarcogyps being clearly the most primitive of the four. All four, together with Gyps and Necrosyrtes, form a monophyletic subfamily or 'core group', to which the subfamily Aegypiinae should be restricted. This group shares a more recent common ancestor with several non-vulture genera of Accipitrids, among them Buteo, Aquila, Haliaeetus and Circaetus, than it does with the two aberrent vultures Gypaetus barbatus and Neophron percnopterus. The last two are much more primitive; they seem to be each other's sister species and are closer to Pernis than to other Accipitrids. We propose separating Gypaetus and Neophron in the subfamily Gypaetinae. If the cytochrome b gene tree accurately reflects vulture phylogeny, Old World vultures are polyphyletic with the Aegypius-Gyps clade having evolved convergently to the more ancient Gypaetus and Neophron vultures. Polyphyly of Old World vultures, although in conflict with the DNA-DNA hybridization phylogeny of Sibley & Ahlquist (1990), is well supported by molecular, karyotypic, morphological and other phenotypic evidence (behaviour, voice) indicating fundamental differences between the two evolutionary lines.
基于线粒体细胞色素b基因的1026个核苷酸,对11种旧大陆秃鹫(鸟纲:鹰形目,兀鹰亚科)、3种新大陆秃鹫(美洲鹫科)及其在鹰形目内外的近缘亲属的系统发育进行了研究。数据支持新大陆秃鹫不是猛禽这一观点,但系统发育信息不足以确定它们与鹳(鹳科)还是与鹰形目关系更近。4种兀鹫属的秃鹫都密切相关,可能在更新世内形成了物种分化。分子数据不支持将“白背”秃鹫从兀鹫属中分离出来归入单独的伪兀鹫属。大型、喙重的秃鹫单型属,如皱脸秃鹫属、兀鹫属、白头秃鹫属和肉垂秃鹫属,都起源于单系。我们建议将兀鹫属与皱脸秃鹫属合并,但保留白头秃鹫属和肉垂秃鹫属为独立的属,肉垂秃鹫属显然是这四个属中最原始的。这四个属与兀鹫属和白背兀鹫属一起,形成了一个单系亚科或“核心类群”,兀鹰亚科应限定为这个类群。与鹰科的几个非秃鹫属,包括鵟属、鹰属、海雕属和短趾雕属相比,这个类群有着更近的共同祖先,而与两种异常的秃鹫胡兀鹫和埃及秃鹫相比则不然。后两者更为原始;它们似乎是彼此的姐妹物种,与蜂鹰属的关系比与其他鹰科动物更近。我们建议将胡兀鹫和埃及秃鹫归入胡兀鹫亚科。如果细胞色素b基因树准确反映秃鹫的系统发育,旧大陆秃鹫是多系的,其中皱脸秃鹫 - 兀鹫进化枝与更古老的胡兀鹫和埃及秃鹫秃鹫趋同进化。旧大陆秃鹫的多系性虽然与西布利和阿尔奎斯特(1990年)的DNA - DNA杂交系统发育相冲突,但分子、核型、形态和其他表型证据(行为、声音)充分支持了这一点,这些证据表明这两个进化谱系之间存在根本差异。