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      Plant palatability and trait responses to experimental warming

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          Abstract

          Climate warming is expected to significantly affect plant–herbivore interactions. Even though direct effects of temperature on herbivores were extensively studied, indirect effects of temperature (acting via changes in host plant quality) on herbivore performance have rarely been addressed. We conducted multiple-choice feeding experiments with generalist herbivore Schistocerca gregaria feeding on six species of genus Impatiens cultivated at three different temperatures in growth chambers and a common garden. We also studied changes in leaf morphology and chemistry. We tested effects of temperature on plant palatability and assessed whether the effects could be explained by changes in the leaf traits. The leaves of most Impatiens species experienced the highest herbivory when cultivated at the warmest temperature. Traits related to leaf morphology (specific leaf area, leaf dry matter content and leaf area), but not to leaf chemistry, partly mediated the effects of temperature on plant palatability. Herbivores preferred smaller leaves with lower specific leaf area and higher leaf dry matter content. Our study suggests that elevated temperature will lead to changes in leaf traits and increase their palatability. This might further enhance the levels of herbivory under the increased herbivore pressure, which is forecasted as a consequence of climate warming.

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          Most cited references70

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          Global patterns of plant leaf N and P in relation to temperature and latitude.

          A global data set including 5,087 observations of leaf nitrogen (N) and phosphorus (P) for 1,280 plant species at 452 sites and of associated mean climate indices demonstrates broad biogeographic patterns. In general, leaf N and P decline and the N/P ratio increases toward the equator as average temperature and growing season length increase. These patterns are similar for five dominant plant groups, coniferous trees and four angiosperm groups (grasses, herbs, shrubs, and trees). These results support the hypotheses that (i) leaf N and P increase from the tropics to the cooler and drier midlatitudes because of temperature-related plant physiological stoichiometry and biogeographical gradients in soil substrate age and then plateau or decrease at high latitudes because of cold temperature effects on biogeochemistry and (ii) the N/P ratio increases with mean temperature and toward the equator, because P is a major limiting nutrient in older tropical soils and N is the major limiting nutrient in younger temperate and high-latitude soils.
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            HERBIVORY AND PLANT DEFENSES IN TROPICAL FORESTS

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              Phenotypic and genetic differentiation between native and introduced plant populations.

              Plant invasions often involve rapid evolutionary change. Founder effects, hybridization, and adaptation to novel environments cause genetic differentiation between native and introduced populations and may contribute to the success of invaders. An influential idea in this context has been the Evolution of Increased Competitive Ability (EICA) hypothesis. It proposes that after enemy release plants rapidly evolve to be less defended but more competitive, thereby increasing plant vigour in introduced populations. To detect evolutionary change in invaders, comparative studies of native versus introduced populations are needed. Here, we review the current empirical evidence from: (1) comparisons of phenotypic variation in natural populations; (2) comparisons of molecular variation with neutral genetic markers; (3) comparisons of quantitative genetic variation in a common environment; and (4) comparisons of phenotypic plasticity across different environments. Field data suggest that increased vigour and reduced herbivory are common in introduced plant populations. In molecular studies, the genetic diversity of introduced populations was not consistently different from that of native populations. Multiple introductions of invasive plants appear to be the rule rather than the exception. In tests of the EICA hypothesis in a common environment, several found increased growth or decreased resistance in introduced populations. However, few provided a full test of the EICA hypothesis by addressing growth and defence in the same species. Overall, there is reasonable empirical evidence to suggest that genetic differentiation through rapid evolutionary change is important in plant invasions. We discuss conceptual and methodological issues associated with cross-continental comparisons and make recommendations for future research. When testing for EICA, greater emphasis should be put on competitive ability and plant tolerance. Moreover, it is important to address evolutionary change in characteristics other than defence and growth that could play a role in plant invasions.
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                Author and article information

                Contributors
                tomas.dostalek@ibot.cas.cz
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                29 June 2020
                29 June 2020
                2020
                : 10
                : 10526
                Affiliations
                [1 ]ISNI 0000 0001 1015 3316, GRID grid.418095.1, Institute of Botany, , The Czech Academy of Sciences, ; Zámek 1, 252 43 Průhonice, Czech Republic
                [2 ]ISNI 0000 0004 1937 116X, GRID grid.4491.8, Department of Botany, Faculty of Science, , Charles University, ; Benátská 2, 128 01 Prague, Czech Republic
                [3 ]ISNI 0000 0001 1015 3316, GRID grid.418095.1, Department of Biodiversity Research, Global Change Research Centre, , The Czech Academy of Sciences, ; Bělidla 4a, 603 00 Brno, Czech Republic
                Author information
                http://orcid.org/0000-0002-3681-5223
                Article
                67437
                10.1038/s41598-020-67437-0
                7324391
                32601471
                b34f5530-6036-4dab-8b06-85bbf6f23f41
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 13 August 2019
                : 8 June 2020
                Funding
                Funded by: FundRef 501100001824, Grantová Agentura České Republiky (Grant Agency of the Czech Republic);
                Award ID: 17-10280S
                Funded by: FundRef 501100004240, Akademie Věd České Republiky (Academy of Sciences of the Czech Republic);
                Award ID: RVO 67985939
                Funded by: FundRef 501100001823, Ministerstvo školství, Mládeže A Tělovýchovy (Ministry of Education, Youth and Sports);
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                plant ecology,climate-change ecology
                Uncategorized
                plant ecology, climate-change ecology

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