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      Reproductive isolation is mediated by pollen incompatibility in sympatric populations of two Arnebia species

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          Abstract

          To explore uncertain aspects of the processes that maintain species boundaries, we evaluated contributions of pre‐ and postpollination reproductive isolation mechanisms in sympatric populations of Arnebia guttata and A. szechenyi. For this, we investigated their phylogenetic relationships, traits, microenvironments, pollinator visits, action of natural selection on floral traits, and the outcome of hand pollination between the two species. Phylogenetic analysis indicates that A. szechenyi is a derived species that could be closely related to A. guttata, and both could be diploid species. Arnebia guttata flowers have larger parts than A. szechenyi flowers, but smaller nectar guides. Soil supporting A. szechenyi had higher water contents than soil supporting neighboring populations of A. guttata (in accordance with their geographical distributions). The pollinators shared by the two species preferred A. szechenyi flowers, but interspecific visitations were frequent. We found evidence of conflicting selection pressures on floral tube length, flower diameter and nectar guide size mediated via male fitness, and on flower diameter and floral tube diameter via female fitness. Hand‐pollination experiments indicate complete pollen incompatibility between the two species. Our results suggest that postpollination prezygotic mechanisms are largely responsible for reproductive isolation of sympatric populations of the two Arnebia species.

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          Sympatric speciation in palms on an oceanic island.

          The origin of species diversity has challenged biologists for over two centuries. Allopatric speciation, the divergence of species resulting from geographical isolation, is well documented. However, sympatric speciation, divergence without geographical isolation, is highly controversial. Claims of sympatric speciation must demonstrate species sympatry, sister relationships, reproductive isolation, and that an earlier allopatric phase is highly unlikely. Here we provide clear support for sympatric speciation in a case study of two species of palm (Arecaceae) on an oceanic island. A large dated phylogenetic tree shows that the two species of Howea, endemic to the remote Lord Howe Island, are sister taxa and diverged from each other well after the island was formed 6.9 million years ago. During fieldwork, we found a substantial disjunction in flowering time that is correlated with soil preference. In addition, a genome scan indicates that few genetic loci are more divergent between the two species than expected under neutrality, a finding consistent with models of sympatric speciation involving disruptive/divergent selection. This case study of sympatric speciation in plants provides an opportunity for refining theoretical models on the origin of species, and new impetus for exploring putative plant and animal examples on oceanic islands.
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            What do we need to know about speciation?

            (2012)
            Speciation has been a major focus of evolutionary biology research in recent years, with many important advances. However, some of the traditional organising principles of the subject area no longer provide a satisfactory framework, such as the classification of speciation mechanisms by geographical context into allopatric, parapatric and sympatry classes. Therefore, we have asked where speciation research should be directed in the coming years. Here, we present a distillation of questions about the mechanisms of speciation, the genetic basis of speciation and the relationship between speciation and diversity. Our list of topics is not exhaustive; rather we aim to promote discussion on research priorities and on the common themes that underlie disparate speciation processes. Copyright © 2011 Elsevier Ltd. All rights reserved.
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              The origins of reproductive isolation in plants.

              Reproductive isolation in plants occurs through multiple barriers that restrict gene flow between populations, but their origins remain uncertain. Work in the past decade has shown that postpollination barriers, such as the failure to form hybrid seeds or sterility of hybrid offspring, are often less strong than prepollination barriers. Evidence implicates multiple evolutionary forces in the origins of reproductive barriers, including mutation, stochastic processes and natural selection. Although adaptation to different environments is a common element of reproductive isolation, genomic conflicts also play a role, including female meiotic drive. The genetic basis of some reproductive barriers, particularly flower colour influencing pollinator behaviour, is well understood in some species, but the genetic changes underlying many other barriers, especially pollen-stylar interactions, are largely unknown. Postpollination barriers appear to accumulate at a faster rate in annuals compared with perennials, due in part to chromosomal rearrangements. Chromosomal changes can be important isolating barriers in themselves but may also reduce the recombination of genes contributing to isolation. Important questions for the next decade include identifying the evolutionary forces responsible for chromosomal rearrangements, determining how often prezygotic barriers arise due to selection against hybrids, and establishing the relative importance of genomic conflicts in speciation.
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                Author and article information

                Journal
                Ecol Evol
                Ecol Evol
                10.1002/(ISSN)2045-7758
                ECE3
                Ecology and Evolution
                John Wiley and Sons Inc. (Hoboken )
                2045-7758
                26 November 2015
                December 2015
                : 5
                : 24 ( doiID: 10.1002/ece3.2015.5.issue-24 )
                : 5838-5846
                Affiliations
                [ 1 ] Key Laboratory for Plant Diversity and Biogeography of East Asia Kunming Institute of BotanyChinese Academy of Sciences Kunming 650201China
                [ 2 ] Plant Germplasm and Genomics Center the Germplasm Bank of Wild Species Kunming Institute of BotanyChinese Academy of Sciences Kunming 650201China
                [ 3 ] Institute of Tibetan Plateau Research at Kunming Kunming Institute of BotanyChinese Academy of Sciences Kunming 650201China
                [ 4 ] College of Life SciencesHenan Normal University Xinxiang 453007 HenanChina
                [ 5 ] Key Laboratory of Biodiversity Conservation in Southwest China of State Forestry AdministrationSouthwest Forestry University Kunming 650224 YunnanChina
                [ 6 ] College of Agriculture and BiotechnologyHexi University Zhangye 734000 GansuChina
                Author notes
                [*] [* ] Correspondence

                Yuan‐Wen Duan, Lanhei Road 132, Heilongtan, Kunming 650201, Yunnan, China.

                Tel/Fax: +86 871 65223231;

                E‐mail: duanyw@ 123456mail.kib.ac.cn

                Article
                ECE31849
                10.1002/ece3.1849
                4717334
                bdebdf71-29fa-4568-b3a1-2c0fff1fee93
                © 2015 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 07 February 2015
                : 21 October 2015
                : 26 October 2015
                Page count
                Pages: 9
                Funding
                Funded by: 973 Programs
                Award ID: 2014CB954100
                Funded by: NSFC
                Award ID: 31270434
                Categories
                Original Research
                Original Research
                Custom metadata
                2.0
                ece31849
                December 2015
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.7.5 mode:remove_FC converted:19.01.2016

                Evolutionary Biology
                floral traits,natural selection,pollen export,pollinator preference,seed set
                Evolutionary Biology
                floral traits, natural selection, pollen export, pollinator preference, seed set

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