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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Plant Sci.</journal-id>
<journal-title>Frontiers in Plant Science</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Plant Sci.</abbrev-journal-title>
<issn pub-type="epub">1664-462X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fpls.2019.00622</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Plant Science</subject>
<subj-group>
<subject>Editorial</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Editorial: Ecoepigenetics in Clonal and Inbreeding Plants: Transgenerational Adaptation and Environmental Variation</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Dong</surname> <given-names>Bi-Cheng</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/294618/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Yu</surname> <given-names>Fei-Hai</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/204452/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Roiloa</surname> <given-names>Sergio R.</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/204855/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>School of Nature Conservation, Beijing Forestry University</institution>, <addr-line>Beijing</addr-line>, <country>China</country></aff>
<aff id="aff2"><sup>2</sup><institution>Institute of Wetland Ecology &#x00026; Clone Ecology / Zhejiang Provincial Key Laboratory of Plant Evolutionary Ecology and Conservation, Taizhou University</institution>, <addr-line>Taizhou</addr-line>, <country>China</country></aff>
<aff id="aff3"><sup>3</sup><institution>BioCost Group, Department of Biology, Faculty of Science, University of A Coru&#x000F1;a</institution>, <addr-line>A Coru&#x000F1;a</addr-line>, <country>Spain</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited and reviewed by: Emidio Albertini, University of Perugia, Italy</p></fn>
<corresp id="c001">&#x0002A;Correspondence: Fei-Hai Yu <email>feihaiyu&#x00040;126.com</email></corresp>
<fn fn-type="other" id="fn001"><p>This article was submitted to Evolutionary and Population Genetics, a section of the journal Frontiers in Plant Science</p></fn></author-notes>
<pub-date pub-type="epub">
<day>15</day>
<month>05</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="collection">
<year>2019</year>
</pub-date>
<volume>10</volume>
<elocation-id>622</elocation-id>
<history>
<date date-type="received">
<day>29</day>
<month>03</month>
<year>2019</year>
</date>
<date date-type="accepted">
<day>26</day>
<month>04</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2019 Dong, Yu and Roiloa.</copyright-statement>
<copyright-year>2019</copyright-year>
<copyright-holder>Dong, Yu and Roiloa</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p></license>
</permissions>
<related-article id="RA1" related-article-type="commentary-article" xlink:href="https://www.frontiersin.org/research-topics/7272/ecoepigenetics-in-clonal-and-inbreeding-plants-transgenerational-adaptation-and-environmental-variation" ext-link-type="uri">Editorial on the Research Topic <article-title>Ecoepigenetics in Clonal and Inbreeding Plants: Transgenerational Adaptation and Environmental Variation</article-title></related-article> 
<kwd-group>
<kwd>clonal growth</kwd>
<kwd>environmental change</kwd>
<kwd>epigenetics</kwd>
<kwd>inbreeding plants</kwd>
<kwd>maternal effect</kwd>
<kwd>transgenerational plasticity</kwd>
</kwd-group>
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<ref-count count="6"/>
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<word-count count="1311"/>
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</front>
<body>
<p>Accelerating global and regional environmental changes are likely to favor species that can rapidly adapt to new conditions. Long-lived, clonal species whose reproduction is mainly asexual have long been thought to possess a relatively low potential for adaptation. However, the potential for transmitting responses to environmental change between vegetative generations within clones could compensate for lack of natural selection based on sexual reproduction (Latzel and Klime&#x00161;ov&#x000E1;, <xref ref-type="bibr" rid="B5">2010</xref>; Douhovnikoff and Dodd, <xref ref-type="bibr" rid="B3">2015</xref>). There are two well-studied mechanisms that underlie transgenerational environmental effects in clonal plants. First, transgenerational environmental effects on clonal (vegetative) offspring may depend on the quality of provisioning, similarly to seeds (Herman and Sultan, <xref ref-type="bibr" rid="B4">2011</xref>; Dong et al., <xref ref-type="bibr" rid="B2">2018</xref>). The relatively large size of clonal offspring may allow for more extensive provisioning with, e.g., carbohydrates or mineral nutrients, thereby obtaining greater fitness. Second, epigenetic changes may encode phenotypic plasticity and allow it to persist between vegetative generations (Dodd and Douhovnikoff, <xref ref-type="bibr" rid="B1">2016</xref>; Richards et al., <xref ref-type="bibr" rid="B6">2017</xref>). Changes such as DNA methylation, chromosome inactivation, and modifications of histones, chromatin, and small non-coding RNAs are now understood to transmit major phenotypic shifts between generations even in the absence of genetically based natural selection. This research topic assembles articles that deal explicitly with the ecological and evolutionary significance of transgenerational environmental effects in clonal plants, and that advance the understanding of the mechanisms of transgenerational effects in clones or inbreeding plants.</p>
<p>Three papers focus on the ecological significance of epigenetic regulation responses for clonal plants to different natural habitats. In a forum paper, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2019.00246">Thiebaut et al.</ext-link> proposed how epigenetic regulation such as DNA methylation could cause chromatin dynamics and silencing, and influenced plant phenotypes, contributing to the adaptation of native plants, in the context of environmental variation. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2018.01635">Broeck et al.</ext-link> showed the relationship between variability of DNA methylation and bud set phenology of the Lombardy poplar (<italic>Populus nigra</italic> cv. <italic>Italica</italic> Duroi) that is widely introduced in Europe. They suggest that epigenetic-based transgenerational inheritance may be relevant for adaption and evolution of <italic>P. nigra</italic> clones in contrasting or rapidly changing environments. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2018.01851">Shi et al.</ext-link> reported that invasive populations of <italic>Alternanthera philoxeroides</italic> in China exhibit extremely low variation in DNA sequence, but high epigenetic diversity. They suggest that epigenetic variation may compensate for the loss of genetic variation in this invasive species and thus contribute to their success in novel environments.</p>
<p>Three papers report parental environmental effects on offspring fitness of clonal plants. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2018.01824">Dong et al.</ext-link> tested effects of parental soil nutrient environments on offspring performance of the highly invasive, clonal herb <italic>A. philoxeroides</italic> at both the individual ramet level and the level of the whole generation of ramets. They provide novel evidence that the magnitude of parental environmental effects varied at different plant levels, and depended on propagule provisioning. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2018.01640">Li et al.</ext-link> examined effects of parental shade environments on growth, morphological and physiological traits of a stoloniferous herb <italic>Centella asiatica</italic>. They found that transgenerational plasticity through both morphological and physiological flexibility was triggered across clonal generations of <italic>C</italic>. <italic>asiatica</italic> subjected to high/low light treatments, and such effects allowed offspring ramets to present adaptive phenotypes in response to the prevailing light environments. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2018.01696">Fan et al.</ext-link> showed that physiological connection with parental ramets of a desert clonal shrub <italic>Calligonum mongolicum</italic> in favorable conditions can alleviate stress on offspring ramets exposed to wind erosion.</p>
<p>Two papers consider the variation in transgenerational environmental effects among genotypes. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2018.01677">Gonz&#x000E1;lez et al.</ext-link> examined the generality of transgenerational environmental effects in the clonal plant <italic>Trifolium repens</italic> with five genotypes and five types of parental environments. They found that transgenerational environmental effects were highly genotype-specific and common in some genotypes, and potentially under epigenetic control. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2018.01251">Baker et al.</ext-link> set up two glasshouse shade environments for an inbreeding plant <italic>Polygonum persicaria</italic>, and measured ecological important traits of their isogenic offspring in both environments. They found that the adaptive effects of parental shading were pronounced and highly significant for seedlings growing under shade, and such effects were mediated by DNA methylation status of parent plants, rather than changes to propagule provisioning.</p>
<p>Transgenerational environmental effects in sexually reproduced species have received considerable attention, but such effects in clonal plants have begun to attract interest. Researchers are recently attempting to advance understanding of the mechanisms for transgenerational environmental effects between vegetative generations, in the context of environmental variation. Clonal plants are widely distributed in nature and dominate a number of plant communities and ecosystems around the world. Therefore, knowledge of transgenerational environmental effects is important to understand how clonal plants can adapt efficiently to the ongoing, rapid change at both global and regional scales in natural environments. We hope the publication of this research topic will stimulate more studies on this important issue in the coming years.</p>
<sec id="s1">
<title>Author Contributions</title>
<p>All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.</p>
<sec>
<title>Conflict of Interest Statement</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p></sec></sec>
</body>
<back>
<ack><p>Research was supported by grants from the National Key Research and Development Program of China (2016YFC1201100) and the Fundamental Research Funds for the Central Universities (2015ZCQ-BH-01) to F-HY, and the National Natural Science Foundation of China (31500331) to B-CD.</p>
</ack>
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