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本文引用的文献

1
Secondary contact seeds phenotypic novelty in cichlid fishes.二次接触引发了丽鱼科鱼类的表型新奇性。
Proc Biol Sci. 2015 Jan 7;282(1798):20142272. doi: 10.1098/rspb.2014.2272.
2
Molecular and fossil evidence place the origin of cichlid fishes long after Gondwanan rifting.分子和化石证据表明,慈鲷鱼起源于冈瓦纳大陆分裂很久之后。
Proc Biol Sci. 2013 Sep 18;280(1770):20131733. doi: 10.1098/rspb.2013.1733. Print 2013 Nov 7.
3
DAMBE5: a comprehensive software package for data analysis in molecular biology and evolution.DAMBE5:一个用于分子生物学和进化数据分析的综合软件包。
Mol Biol Evol. 2013 Jul;30(7):1720-8. doi: 10.1093/molbev/mst064. Epub 2013 Apr 5.
4
Mitochondrial genome primers for Lake Malawi cichlids.线粒体基因组引物用于马拉维湖慈鲷。
Mol Ecol Resour. 2013 May;13(3):347-53. doi: 10.1111/1755-0998.12066. Epub 2013 Jan 25.
5
Origins of shared genetic variation in African cichlids.非洲慈鲷共享遗传变异的起源。
Mol Biol Evol. 2013 Apr;30(4):906-17. doi: 10.1093/molbev/mss326. Epub 2012 Dec 28.
6
Repeated trans-watershed hybridization among haplochromine cichlids (Cichlidae) was triggered by Neogene landscape evolution.新第三纪地貌演化引发了haplochromine 丽鱼科(慈鲷科)的跨流域杂交。
Proc Biol Sci. 2012 Nov 7;279(1746):4389-98. doi: 10.1098/rspb.2012.1667. Epub 2012 Sep 5.
7
The impact of the geologic history and paleoclimate on the diversification of East african cichlids.地质历史和古气候对东非丽鱼科鱼类多样化的影响。
Int J Evol Biol. 2012;2012:574851. doi: 10.1155/2012/574851. Epub 2012 Jul 19.
8
Genome-wide patterns of standing genetic variation in a marine population of three-spined sticklebacks.三刺鱼海洋种群中广泛存在的遗传变异的全基因组模式。
Mol Ecol. 2013 Feb;22(3):635-49. doi: 10.1111/j.1365-294X.2012.05680.x. Epub 2012 Jul 3.
9
Bayesian phylogenetics with BEAUti and the BEAST 1.7.贝叶斯系统发育学与 BEAUTi 和 BEAST 1.7。
Mol Biol Evol. 2012 Aug;29(8):1969-73. doi: 10.1093/molbev/mss075. Epub 2012 Feb 25.
10
Partitionfinder: combined selection of partitioning schemes and substitution models for phylogenetic analyses.Partitionfinder:用于系统发育分析的分区方案和替代模型的联合选择。
Mol Biol Evol. 2012 Jun;29(6):1695-701. doi: 10.1093/molbev/mss020. Epub 2012 Jan 20.

马拉维湖丽鱼多样性的地理起源。

Geographical ancestry of Lake Malawi's cichlid fish diversity.

作者信息

Genner Martin J, Ngatunga Benjamin P, Mzighani Semvua, Smith Alan, Turner George F

机构信息

School of Biological Sciences, University of Bristol, Life Sciences Building, Bristol BS81TQ, UK

Tanzania Fisheries Research Institute (TAFIRI), PO Box 9750, Dar-es-Salaam, Tanzania.

出版信息

Biol Lett. 2015 Jun;11(6):20150232. doi: 10.1098/rsbl.2015.0232.

DOI:10.1098/rsbl.2015.0232
PMID:26063752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4528473/
Abstract

The Lake Malawi haplochromine cichlid flock is one of the largest vertebrate adaptive radiations. The geographical source of the radiation has been assumed to be rivers to the south and east of Lake Malawi, where extant representatives of the flock are now present. Here, we provide mitochondrial DNA evidence suggesting the sister taxon to the Lake Malawi radiation is within the Great Ruaha river in Tanzania, north of Lake Malawi. Estimates of the time of divergence between the Lake Malawi flock and this riverine sister taxon range from 2.13 to 6.76 Ma, prior to origins of the current radiation 1.20-4.06 Ma. These results are congruent with evaluations of 2-3.75 Ma fossil material that suggest past faunal connections between Lake Malawi and the Ruaha. We propose that ancestors of the Malawi radiation became isolated within the catchment during Pliocene rifting that formed both Lake Malawi and the Kipengere/Livingstone mountain range, before colonizing rivers to the south and east of the lake region and radiating within the lake basin. Identification of this sister taxon allows tests of whether standing genetic diversity has predisposed Lake Malawi cichlids to rapid speciation and adaptive radiation.

摘要

马拉维湖丽鱼科辐鳍鱼群是最大的脊椎动物适应性辐射之一。人们一直认为这种辐射的地理源头是马拉维湖以南和以东的河流,该鱼群现存的代表如今就在那里。在此,我们提供线粒体DNA证据表明,马拉维湖辐射的姐妹分类单元位于马拉维湖以北的坦桑尼亚大鲁阿哈河中。马拉维湖鱼群与这个河流姐妹分类单元之间的分化时间估计在213万至676万年前,早于当前辐射起源的120万至406万年前。这些结果与对200万至375万年前化石材料的评估结果一致,这些评估表明马拉维湖和鲁阿哈河过去存在动物区系联系。我们提出,马拉维辐射的祖先在形成马拉维湖和基彭盖雷/利文斯通山脉的上新世裂谷期间,在集水区内被隔离,之后才在湖区以南和以东的河流中定殖,并在湖盆内辐射。识别这个姐妹分类单元有助于检验现存的遗传多样性是否使马拉维湖丽鱼易于快速物种形成和适应性辐射。