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      Directional selection for flowering time leads to adaptive evolution in Raphanus raphanistrum (Wild radish)

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          Abstract

          Herbicides have been the primary tool for controlling large populations of yield depleting weeds from agro‐ecosystems, resulting in the evolution of widespread herbicide resistance. In response, nonherbicidal techniques have been developed which intercept weed seeds at harvest before they enter the soil seed bank. However, the efficiency of these techniques allows an intense selection for any trait that enables weeds to evade collection, with early‐flowering ecotypes considered likely to result in early seed shedding. Using a field‐collected wild radish population, five recurrent generations were selected for early maturity and three generations for late maturity. Phenology associated with flowering time and growth traits were measured. Our results demonstrate the adaptive capacity of wild radish to halve its time to flowering following five generations of early‐flowering selection. Early‐maturing phenotypes had reduced height and biomass at maturity, leading to less competitive, more prostrate growth forms. Following three generations of late‐flowering selection, wild radish doubled its time to flowering time leading to increased biomass and flowering height at maturity. This study demonstrates the potential for the rapid evolution in growth traits in response to highly effective seed collection techniques that imposed a selection on weed populations within agro‐ecosystems at harvest.

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          Arabidopsis, the Rosetta stone of flowering time?

          Multiple environmental and endogenous inputs regulate when plants flower. The molecular genetic dissection of flowering time control in Arabidopsis has identified an integrated network of pathways that quantitatively control the timing of this developmental switch. This framework provides the basis to understand the evolution of different reproductive strategies and how floral pathways interact through seasonal progression.
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            Why have no new herbicide modes of action appeared in recent years?

            Herbicides with new modes of action are badly needed to manage the evolution of resistance of weeds to existing herbicides. Yet no major new mode of action has been introduced to the market place for about 20 years. There are probably several reasons for this. New potential products may have remained dormant owing to concerns that glyphosate-resistant (GR) crops have reduced the market for a new herbicide. The capture of a large fraction of the herbicide market by glyphosate with GR crops led to significantly diminished herbicide discovery efforts. Some of the reduced herbicide discovery research was also due to company consolidations and the availability of more generic herbicides. Another problem might be that the best herbicide molecular target sites may have already been discovered. However, target sites that are not utilized, for which there are inhibitors that are highly effective at killing plants, suggests that this is not true. Results of modern methods of target site discovery (e.g. gene knockout methods) are mostly not public, but there is no evidence of good herbicides with new target sites coming from these approaches. In summary, there are several reasons for a long dry period for new herbicide target sites; however, the relative magnitude of each is unclear. The economic stimulus to the herbicide industry caused by the evolution of herbicide-resistant weeds, especially GR weeds, may result in one or more new modes of action becoming available in the not too distant future. Copyright © 2011 Society of Chemical Industry.
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              Plasticity and evolution in drought avoidance and escape in the annual plant Brassica rapa.

              A key question in ecological genetics is to what extent do plants adapt to changes in climatic conditions, such as drought, through plasticity or evolution. To address this question, seeds of 140 maternal families of Brassica rapa were generated from collections made before (1997) and after (2004) a natural drought. These seeds were planted in the glasshouse and grown under low-water and high-water conditions. Post-drought lines flowered earlier than pre-drought lines, showing an evolutionary shift to earlier flowering. There was significant genetic variation and genotype by environment (G × E) interactions in flowering time, indicating genetic variation in plasticity in this trait. Plants that flowered earlier had fewer leaf nodes and lower instantaneous (A/g) and integrated (δ(13)C) water use efficiency than late-flowering plants. These results suggest that B. rapa plants escape drought through early flowering rather than avoid drought through increased water use efficiency. The mechanism of this response appears to be high transpiration and inefficient water use, leading to rapid development. These findings demonstrate a trade-off between drought avoidance and escape, and indicate that, in this system, where drought acts to shorten the growing season, selection for drought escape through earlier flowering is more important than phenotypic plasticity. © 2011 The Author. New Phytologist © 2011 New Phytologist Trust.
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                Author and article information

                Journal
                Evol Appl
                Evol Appl
                10.1111/(ISSN)1752-4571
                EVA
                Evolutionary Applications
                John Wiley and Sons Inc. (Hoboken )
                1752-4571
                17 February 2016
                April 2016
                : 9
                : 4 ( doiID: 10.1111/eva.2016.9.issue-4 )
                : 619-629
                Affiliations
                [ 1 ] Australian Herbicide Resistance Initiative School of Plant BiologyThe University of Western Australia Crawley WAAustralia
                [ 2 ] Department of Agriculture and Environment School of ScienceCurtin University Bentley WAAustralia
                [ 3 ] School of Plant BiologyThe University of Western Australia Crawley WAAustralia
                [ 4 ] IFEVA‐CONICET Facultad de AgronomíaUniversidad de Buenos Aires Buenos AiresArgentina
                Author notes
                [*] [* ] Correspondence

                Stephen B. Powles, Australian Herbicide Resistance Initiative, School of Plant Biology, The University of Western Australia, Crawley, WA 6009, Australia.

                Tel.: +61 8 64887833;

                Fax: +61 8 64887834;

                e‐mail: stephen.powles@ 123456uwa.edu.au

                Article
                EVA12350
                10.1111/eva.12350
                4831463
                27099626
                c8c32b7d-e3cf-4829-8ef5-4321c800e528
                © 2015 The Authors. Evolutionary Applications 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
                : 05 August 2015
                : 29 November 2015
                Page count
                Pages: 11
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                eva12350
                April 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.8.6 mode:remove_FC converted:09.04.2016

                Evolutionary Biology
                biomass,evolution,flowering height,flowering time,phenotypic resistance,wild radish

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