INRA, UMR Centre de Biologie pour la Gestion des Populations, CBGP, (INRA/IRD/CIRAD/Montpellier SupAgro), Campus International de Baillarguet, CS30016, 34988, Montferrier-sur-Lez, France.
BMC Evol Biol. 2012 Jun 12;12:82. doi: 10.1186/1471-2148-12-82.
The temporal and geographical diversification of Neotropical insects remains poorly understood because of the complex changes in geological and climatic conditions that occurred during the Cenozoic. To better understand extant patterns in Neotropical biodiversity, we investigated the evolutionary history of three Neotropical swallowtail Troidini genera (Papilionidae). First, DNA-based species delimitation analyses were conducted to assess species boundaries within Neotropical Troidini using an enlarged fragment of the standard barcode gene. Molecularly delineated species were then used to infer a time-calibrated species-level phylogeny based on a three-gene dataset and Bayesian dating analyses. The corresponding chronogram was used to explore their temporal and geographical diversification through distinct likelihood-based methods.
The phylogeny for Neotropical Troidini was well resolved and strongly supported. Molecular dating and biogeographic analyses indicate that the extant lineages of Neotropical Troidini have a late Eocene (33-42 Ma) origin in North America. Two independent lineages (Battus and Euryades+Parides) reached South America via the GAARlandia temporary connection, and later became extinct in North America. They only began substantive diversification during the early Miocene in Amazonia. Macroevolutionary analysis supports the "museum model" of diversification, rather than Pleistocene refugia, as the best explanation for the diversification of these lineages.
This study demonstrates that: (i) current Neotropical biodiversity may have originated ex situ; (ii) the GAARlandia bridge was important in facilitating invasions of South America; (iii) colonization of Amazonia initiated the crown diversification of these swallowtails; and (iv) Amazonia is not only a species-rich region but also acted as a sanctuary for the dynamics of this diversity. In particular, Amazonia probably allowed the persistence of old lineages and contributed to the steady accumulation of diversity over time with constant net diversification rates, a result that contrasts with previous studies on other South American butterflies.
由于新生代地质和气候条件的复杂变化,新热带昆虫的时间和地理多样化仍知之甚少。为了更好地了解新热带生物多样性的现存模式,我们调查了三个新热带燕尾蝶 Troidini 属(凤蝶科)的进化历史。首先,使用标准条形码基因的扩大片段进行基于 DNA 的物种界限分析,以评估新热带 Troidini 内的物种边界。然后,使用分子界定的物种基于三基因数据集和贝叶斯定年分析推断出时间校准的种系发生树。相应的时标用于通过不同的似然基方法探索它们的时间和地理多样化。
新热带燕尾蝶 Troidini 的系统发育得到了很好的解决并得到了强烈支持。分子定年和生物地理学分析表明,现存的新热带 Troidini 谱系起源于晚始新世(33-42 Ma)在北美的起源。两个独立的谱系(Battus 和 Euryades+Parides)通过 GAARlandia 临时连接到达南美洲,后来在北美的灭绝。它们仅在早中新世在亚马逊地区开始实质性多样化。宏观进化分析支持多样化的“博物馆模型”,而不是更新世避难所,是这些谱系多样化的最佳解释。
这项研究表明:(i)当前的新热带生物多样性可能起源于异地;(ii)GAARlandia 桥对于南美的入侵很重要;(iii)亚马逊地区的殖民化启动了这些燕尾蝶的冠部多样化;(iv)亚马逊地区不仅是一个物种丰富的地区,而且还是这种多样性动态的避难所。特别是,亚马逊地区可能允许旧谱系的持续存在,并有助于随着时间的推移不断积累多样性,具有恒定的净多样化率,这与之前对其他南美的蝴蝶的研究结果形成对比。