Table 1.
Summary of the effects of elevated CO2, drought, high temperature and salinity on physiological, morphological and molecular characteristics of potato and acclimation/adaptation strategies.
Responses to change in the growth environment |
Acclimation/ Adaptation strategies | |||
---|---|---|---|---|
Morphological | Physiological | Molecular | ||
High CO2 | • Increased plant biomass | • Increased photosynthesis | • Down-regulation of key | • Stomatal closure |
• Resource remobilization particularly nitrogen in plant | ||||
• Increased tuber yield | • Changed respiration rates | • photosynthetic enzyme activities particularly RuBisCO. | ||
• Changed photorespiration rates | ||||
• Decreased RuBisCO activity | ||||
• Increased LAI | ||||
• Reduced stomatal conductance | ||||
• Increased leaf DM content | ||||
• Reduced transpiration rates | ||||
• Increased water use efficiency | ||||
• Accumulation of non-soluble carbohydrates. | ||||
• Increased leaf nitrogen content | ||||
Drought | • Reduced plant growth | • Declined photosynthesis | • Up-regulation of drought-responsive gene expression | • Stomatal closure |
• Changed respiration rates | • Increased root to shoot ratio. | |||
• Reduced plant biomass | ||||
• Increased ABA synthesis | ||||
• Down-regulation of key photosynthetic gene expression | ||||
• Reduced chlorophyll content | • Increased osmolyte content. | |||
• Reduced tuber yield | • Reduced internal CO2 concentrations | • Reduced activities of key photosynthetic enzymes. | • Increased synthesis of drought-related proteins, | |
• Reduced stolon and tuber number | • Reduced transpiration rates | |||
• Increased activities of starch degrading enzymes | • Narrower leaf with hair. | |||
• Starch mobilization to reducing sugars | ||||
• Increased anti-oxidant | ||||
• Reduced LAI | ||||
• Tuber develops sugar ends | ||||
• Increased glycoalkaloids | ||||
• Increased leaf DM content | ||||
• Tuber develops malformations (hollow heart, cracking and secondary growth) | ||||
• Shorter plant height | ||||
• Increased root to shoot ratio | ||||
• Tuber develops internal brown spot | ||||
• Delayed tuberization | ||||
• Early senescence | ||||
High temperature | • Reduced plant growth | • Declined photosynthesis | • Increased activities of starch degrading enzymes | Increased synthesis of heat-shock proteins |
• Reduced tuber yield | • Reduced photosystem II activity | |||
• Increased transpiration | ||||
• Increased leaf DM content | • Reduced sucrose translocation to tubers. | |||
• Decreased tuber DM content | • Starch mobilization to reducing sugars | |||
• Tuber develops sugar ends | ||||
• Delayed tuberization | ||||
• Tuber develops malformations (hollow heart, cracking and secondary growth) | ||||
• Tuber develops necrosis | ||||
• Tuber develops field sprouting | ||||
Salinity | • Reduced plant emergence | • Declined photosynthesis | • Increased activity of transmembrane transport proteins involved in Na+ transport to vacuole | • Stomatal closure |
• Reduced transpiration rates | • Increased ABA | |||
• Reduced root length and volume | • Increased proline | |||
• Increased Na+ transport across the tonoplast in exchange for H+ | ||||
• Reduced leaf water content | ||||
Early haulm senescence | ||||
• Reduced activities of nitrate reductase | ||||
• Increased activity of antioxidant enzymes; ascorbate peroxidise, catalase, glutathione reductase and hydrogen peroxide | ||||
• Reduced leaf osmotic potential | ||||
• Down-regulation of genes coding for Photosystem I, Photosystem II and chlorophyll synthesis proteins | ||||
• Reduced shoot biomass | • Increased total soluble solids | |||
Increased lipid peroxidation | ||||
• Reduced tuber growth | ||||
• Change in chloroplast ultra-structure | ||||
• Increased leaf carbohydrate content | ||||
• Decreased tuber DM content | ||||
• Reduced tuber nitrogen content | • Change in gene expression related to carbohydrate and amino acid metabolism | |||
• Reduced tuber number | ||||
• Reduced tuber yield | ||||
LAI, Leaf area index; DM, dry matter. Data were obtained from: High CO2 (Sage et al., 1989; Mackowiak and Wheeler, 1996; Sicher and Bunce, 2001; Donnelly et al., 2001; Vandermeiren et al., 2002; Magliulo et al., 2003; Katny et al., 2005; Kaminski et al., 2014); Drought (Dalla Costa et al., 1997; Chen and Murata, 2008; Evers et al., 2010; Watanabe et al., 2011; Albiski et al., 2012; Wang-Pruski and Schofield, 2012; Obidiegwu et al., 2015; Zarzynska et al., 2017); High temperature (Burton, 1981; Hijmans, 2003; Timlin et al., 2006; Levy and Veilleux, 2007; Minhas, 2012; Bita and Gerats, 2013; Hancock et al., 2014; Rykaczewska, 2015; Tang et al., 2016; Trapero-Mozos et al., 2018); Salinity (Levy et al., 1988; Levy, 1992; Ghosh et al., 2001; Fidalgo et al., 2004; Aghaei et al., 2009; Legay et al., 2009;Queirós et al., 2009a,b, 2011; Akhtar et al., 2015; Jaarsma and de Boer, 2018).