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      Chilling and frost tolerance in Miscanthus and Saccharum genotypes bred for cool temperate climates

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          Summary

          Triploid Miscanthus hybrids have superior chilling tolerance across Miscanthus and Saccharum genotypes bred for cool temperate climates.

          Abstract

          Miscanthus hybrids are leading candidates for bioenergy feedstocks in mid to high latitudes of North America and Eurasia, due to high productivity associated with the C 4 photosynthetic pathway and their tolerance of cooler conditions. However, as C 4 plants, they may lack tolerance of chilling conditions (0–10 °C) and frost, particularly when compared with candidate C 3 crops at high latitudes. In higher latitudes, cold tolerance is particularly important if the feedstock is to utilize fully the long, early-season days of May and June. Here, leaf gas exchange and fluorescence are used to assess chilling tolerance of photosynthesis in five Miscanthus hybrids bred for cold tolerance, a complex Saccharum hybrid (energycane), and an upland sugarcane variety with some chilling tolerance. The chilling treatment consisted of transferring warm-grown plants (25/20 °C day/night growth temperatures) to chilling (12/5 °C) conditions for 1 week, followed by assessing recovery after return to warm temperatures. Chilling tolerance was also evaluated in outdoor, spring-grown Miscanthus genotypes before and after a cold front that was punctuated by a frost event. Miscanthus×giganteus was found to be the most chilling-tolerant genotype based on its ability to maintain a high net CO 2 assimilation rate ( A) during chilling, and recover A to a greater degree following a return to warm conditions. This was associated with increasing its capacity for short-term dark-reversible photoprotective processes (Φ REG) and the proportion of open photosystem II reaction centres (qL) while minimizing photoinactivation (Φ NF). Similarly, in the field, M.×giganteus exhibited a significantly greater A and pre-dawn F v/ F m after the cold front compared with the other chilling-sensitive Miscanthus hybrids.

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          Most cited references14

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          Chlorophyll fluorescence--a practical guide.

          Chlorophyll fluorescence analysis has become one of the most powerful and widely used techniques available to plant physiologists and ecophysiologists. This review aims to provide an introduction for the novice into the methodology and applications of chlorophyll fluorescence. After a brief introduction into the theoretical background of the technique, the methodology and some of the technical pitfalls that can be encountered are explained. A selection of examples is then used to illustrate the types of information that fluorescence can provide.
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            New fluorescence parameters for the determination of q(a) redox state and excitation energy fluxes.

            A number of useful photosynthetic parameters are commonly derived from saturation pulse-induced fluorescence analysis. We show, that q(P), an estimate of the fraction of open centers, is based on a pure 'puddle' antenna model, where each Photosystem (PS) II center possesses its own independent antenna system. This parameter is incompatible with more realistic models of the photosynthetic unit, where reaction centers are connected by shared antenna, that is, the so-called 'lake' or 'connected units' models. We thus introduce a new parameter, q(L), based on a Stern-Volmer approach using a lake model, which estimates the fraction of open PS II centers. We suggest that q(L) should be a useful parameter for terrestrial plants consistent with a high connectivity of PS II units, whereas some marine species with distinct antenna architecture, may require the use of more complex parameters based on intermediate models of the photosynthetic unit. Another useful parameter calculated from fluorescence analysis is Phi(II), the yield of PS II. In contrast to q(L), we show that the Phi(II) parameter can be derived from either a pure 'lake' or pure 'puddle' model, and is thus likely to be a robust parameter. The energy absorbed by PS II is divided between the fraction used in photochemistry, Phi(II), and that lost non-photochemically. We introduce two additional parameters that can be used to estimate the flux of excitation energy into competing non-photochemical pathways, the yield induced by downregulatory processes, Phi(NPQ), and the yield for other energy losses, Phi(NO).
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              Photoprotection in plants: a new light on photosystem II damage.

              Sunlight damages photosynthetic machinery, primarily photosystem II (PSII), and causes photoinhibition that can limit plant photosynthetic activity, growth and productivity. The extent of photoinhibition is associated with a balance between the rate of photodamage and its repair. Recent studies have shown that light absorption by the manganese cluster in the oxygen-evolving complex of PSII causes primary photodamage, whereas excess light absorbed by light-harvesting complexes acts to cause inhibition of the PSII repair process chiefly through the generation of reactive oxygen species. As we review here, PSII photodamage and the inhibition of repair are therefore alleviated by photoprotection mechanisms associated with avoiding light absorption by the manganese cluster and successfully consuming or dissipating the light energy absorbed by photosynthetic pigments, respectively. Copyright © 2010 Elsevier Ltd. All rights reserved.
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                Author and article information

                Journal
                J Exp Bot
                J. Exp. Bot
                jexbot
                exbotj
                Journal of Experimental Botany
                Oxford University Press (UK )
                0022-0957
                1460-2431
                July 2014
                18 March 2014
                18 March 2014
                : 65
                : 13 , Special Issue: C4 and CAM Photosynthesis in the New Millenium
                : 3749-3758
                Affiliations
                1Department of Ecology and Evolutionary Biology, University of Toronto , 25 Willcocks Street, Toronto, Ontario, Canada, M5S 3B2
                2Plant Science Division, Research School of Biology, Australian National University , Canberra, ACT, 0200Australia
                3Department of Cell and Systems Biology, University of Toronto , 25 Harbord Street, Toronto, Ontario, Canada, M5S 3G5
                Author notes
                * To whom correspondence should be addressed. E-mail: patrick.friesen@ 123456utoronto.ca
                Article
                10.1093/jxb/eru105
                4085960
                24642848
                998fdbe4-4490-4133-beb6-3c1992c51d98
                © The Author 2014. Published by Oxford University Press on behalf of the Society for Experimental Biology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                Page count
                Pages: 10
                Categories
                Research Paper

                Plant science & Botany
                chilling tolerance,chlorophyll fluorescence,gas exchange,miscanthus,perennial c4 grasses,photosynthesis,saccharum.

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