Ruiz-García Manuel, Luengas-Villamil Kelly, Leguizamon Norberto, de Thoisy Benoit, Gálvez Hugo
Unidad de Genética. Laboratorio de Genética de Poblaciones-Biología Evolutiva. Departamento de Biología. Facultad de Ciencias, Pontificia Universidad Javeriana, Cra 7A No 43-82, Bogotá, DC, Colombia,
Primates. 2015 Apr;56(2):145-61. doi: 10.1007/s10329-014-0452-0. Epub 2014 Oct 28.
Some previous genetic studies have been performed to resolve the molecular phylogenetics of the squirrel monkeys (Saimiri). However, these studies did not show consensus in how many taxa are within this genus and what the relationships among them are. For this reason, we sequenced 2,237 base pairs of the mt COI and COII genes in 218 Saimiri individuals. All, less 12 S. sciureus sciureus from French Guyana, were sampled in the wild. These samples represented all the living Saimiri taxa recognized. There were four main findings of this study. (1) Our analysis detected 17 different Saimiri groups: albigena, cassiquiarensis, five polyphyletic macrodon groups, three polyphyletic ustus groups, sciureus, collinsi, boliviensis, peruviensis, vanzolinii, oerstedii and citrinellus. Four different phylogenetic trees showed the Central American squirrel monkey (S. oerstedii) as the most differentiated taxon. In contrast, albigena was indicated to be the most recent taxon. (2) There was extensive hybridization and/or historical introgression among albigena, different macrodon groups, peruviensis, sciureus and collinsi. (3) Different tests showed that our maximum likelihood tree was consistent with two species of Saimiri: S. oerstedii and S. sciureus. If no cases of hybridization were detected implicating S. vanzolinii, this could be a third recognized species. (4) We also estimated that the first temporal splits within this genus occurred around 1.4-1.6 million years ago, which indicates that the temporal split events within Saimiri were correlated with Pleistocene climatic changes. If the biological species concept is applied because, in this case, it is operative due to observed hybridization in the wild, the number of species within this genus is probably more limited than recently proposed by other authors. The Pleistocene was the fundamental epoch when the mitochondrial Saimiri diversification process occurred.
此前已有一些遗传学研究旨在解析松鼠猴属(Saimiri)的分子系统发育。然而,这些研究在该属内包含多少分类单元以及它们之间的关系如何等问题上并未达成共识。因此,我们对218只松鼠猴个体的线粒体细胞色素氧化酶亚基I(mt COI)和细胞色素氧化酶亚基II(COII)基因的2237个碱基对进行了测序。除了来自法属圭亚那的12只红背松鼠猴指名亚种(S. sciureus sciureus)外,其他所有样本均采自野外。这些样本代表了所有已被认可的现存松鼠猴分类单元。本研究有四项主要发现。(1)我们的分析检测到17个不同的松鼠猴群体:白腹松鼠猴(albigena)、卡西基亚雷松鼠猴(cassiquiarensis)、五个多系的大牙松鼠猴(macrodon)群体、三个多系的乌斯图松鼠猴(ustus)群体、红背松鼠猴(sciureus)、科林斯松鼠猴(collinsi)、玻利维亚松鼠猴(boliviensis)、秘鲁松鼠猴(peruviensis)、万佐利尼松鼠猴(vanzolinii)、奥氏松鼠猴(oerstedii)和柠檬色松鼠猴(citrinellus)。四棵不同的系统发育树显示中美洲松鼠猴(S. oerstedii)是分化程度最高的分类单元。相比之下,白腹松鼠猴被认为是最新的分类单元。(2)白腹松鼠猴、不同的大牙松鼠猴群体、秘鲁松鼠猴、红背松鼠猴和科林斯松鼠猴之间存在广泛的杂交和/或历史基因渗入。(3)不同的检验表明,我们的最大似然树与两种松鼠猴一致:奥氏松鼠猴和红背松鼠猴。如果未检测到涉及万佐利尼松鼠猴的杂交情况,那么它可能是第三个被认可的物种。(4)我们还估计该属内的首次时间分化发生在约140万至160万年前,这表明松鼠猴属内的时间分化事件与更新世气候变化相关。如果应用生物物种概念,因为在这种情况下,由于在野外观察到杂交现象它是适用的,那么该属内的物种数量可能比其他作者最近提出的更有限。更新世是线粒体松鼠猴多样化过程发生的关键时期。