Gunderson, C. A., O’Hara, K. H., Campion, C. M., Waler, A. V. & Edwards, N. T. Thermal plasticity of photosynthesis: The role of acclimation in forest responses to a warming climate. Glob. Change Biol. 16, 2272–2286 (2010).
Google Scholar
Sage, R. F., Way, D. A. & Kubien, D. S. Rubisco, Rubisco activase, and global climate change. J. Exp. Bot. 59, 1581–1595 (2008).
Google Scholar
Sendall, K. M. et al. Acclimation of photosynthetic temperature optima of temperate and boreal tree species in response to experimental forest warming. Glob. Change Biol. 21, 1342–1357 (2015).
Google Scholar
IPCC AR5. Climate Change 2013: The Physical Science Basis. Contribution of Working Group I to the Fourth Assessment Report to the Intergovernmental Panel on Climate Change (Cambridge University Press, 2013).
Atkin, O. K. et al. 2008 Using temperature-dependent changes in leaf scaling relationships to quantitatively account for thermal acclimation of respiration in a coupled global climate–vegetation model. Glob. Change Biol. 14, 2709–2726 (2008).
Google Scholar
Reich, P. B. et al. Boreal and temperate trees show strong acclimation of respiration to warming. Nature 531, 633–636 (2016).
Google Scholar
Hikosaka, H., Ishikawa, K., Borjigidai, A., Muller, O. & Onoda, Y. Temperature acclimation of photosynthesis: Mechanisms involved in the changes in temperature dependence of photosynthetic rate. J. Exp. Bot. 57, 291–302 (2006).
Google Scholar
Ow, L. F., Griffin, K. L., Whitehead, D., Walcroft, A. S. & Turnbull, M. H. Thermal acclimation of leaf respiration but not photosynthesis in Populus deltoides × nigra. New Phytol. 178, 123–134 (2008).
Google Scholar
Way, D. A. & Yamori, W. Thermal acclimation of photosynthesis: On the importance of adjusting our definitions and accounting for thermal acclimation of respiration. Photosynth. Res. 119, 89–100 (2014).
Google Scholar
Heskel, M. A. et al. Convergence in the temperature response of leaf respiration across biomes and plant functional types. Proc. Natl. Acad. Sci. USA 113, 3832–3837 (2016).
Google Scholar
Sage, R. F. & Kubien, D. S. The temperature response of C3 and C4 photosynthesis. Plant Cell Environ. 30, 1086–1106 (2007).
Google Scholar
Scafaro, A. P. et al. Strong thermal acclimation of photosynthesis in tropical and temperate wet-forest tree species: the importance of altered Rubisco content. Glob. Change Biol. 23, 2783–2800 (2017).
Google Scholar
Higgins, S. I. & Richardson, D. M. Predicting plant migration rates in a changing world: the role of long-distance dispersal. Am. Nat. 153, 464–475 (1999).
Google Scholar
Atkin, O. K. & Tjoelker, M. G. Thermal acclimation and the dynamic response of plant respiration to temperature. Trend. Plant Sci. 8, 343–351 (2003).
Google Scholar
Yamori, W., Hikosaka, K. & Way, D. A. Temperature response of photosynthesis in C3, C4, and CAM plants: temperature acclimation and temperature adaptation. Photosynth. Res. 119, 101–117 (2014).
Google Scholar
Atkin, O. K. et al. Global variability in leaf respiration in relation to climate, plant functional types and leaf traits. New Phytol. 206, 614–636 (2015).
Google Scholar
Slot, M. & Kitajima, K. General patterns of acclimation of leaf respiration to elevated temperatures across biomes and plant types. Oecologia 177, 885–900 (2015).
Google Scholar
Atkinson, L. J., Hellicar, M. A., Fitter, A. H. & Atkin, O. K. Impact of temperature on the relationship between respiration and nitrogen concentration in roots: An analysis of scaling relationships, Q10 values and thermal acclimation ratios. New Phytol. 173, 110–120 (2007).
Google Scholar
Wei, X. et al. Consistent leaf respiratory response to experimental warming of three North American deciduous trees: A comparison across seasons, years, habitats and sites. Tree Physiol. 37, 285–300 (2017).
Google Scholar
Kruse, J., Hopmans, P. & Adams, M. A. Temperature responses are a window to the physiology of dark respiration: Differences between CO2 release and O2 reduction shed light on energy conservation. Plant Cell Environ. 31, 901–914 (2008).
Google Scholar
Kruse, J., Rennenberg, H. & Adams, M. A. Steps towards a mechanistic understanding of respiratory temperature responses. New Phytol. 189, 659–677 (2011).
Google Scholar
Kakishima, S., Yoshimura, J., Murata, H. & Murata, J. 6-year periodicity and variable synchronicity in a mass-flowering plant. PLoS ONE 6, e28140. https://doi.org/10.1371/journal.pone.002814 (2011).
Google Scholar
Kakishima, S. et al. Evolutionary origin of a periodical mass-flowering plant. Ecol. Evol. 9, 4373–4381 (2019).
Google Scholar
Björkman, O. & Denning, B. Photon field of O2 evolution and chlorophyll fluorescence characteristics at 77K among vascular plants of diverse origins. Planta 170, 489–504 (1987).
Google Scholar
Stirling, C. M., Aguilera, C., Baker, N. R. & Long, S. P. Changes in the photosynthetic light response curve during leaf development of field-grown maize with implications for modeling canopy photosynthesis. Photosynth. Res. 42, 217–225 (1994).
Google Scholar
Ishida, A., Uemura, A., Koike, N., Matsumoto, Y. & Ang, L. H. Interactive effects of leaf age and self-shading on leaf structure, photosynthetic capacity and chlorophyll fluorescence in the rain forest tree, Dryobalanops aromatic. Tree Physiol. 19, 741–747 (1999).
Google Scholar
Bouma, T. J. et al. Respiratory energy requirements and rate of protein turnover in vivo determined by the use of an inhibitor of protein synthesis and a probe to assess its effect. Physiol. Plant. 92, 585–594 (1994).
Google Scholar
Noguchi, K. et al. Costs of protein turnover and carbohydrate export in leaves of sun and shade species. Aust. J. Plant Physiol. 28, 37–47 (2001).
Google Scholar
Stephanie, S. Y. et al. Respiratory alternative oxidase responds to both low- and high-temperature stress in Quercus rubra leaves along an urban-rural gradient in New York. Funct. Ecol. 25, 1007–1017 (2011).
Google Scholar
Reich, P. B., Walters, M. B. & Ellsworth, D. S. From tropics to tundra: Global convergence in plant functioning. Proc. Natl. Acad. Sci. USA 94, 13730–13734 (1997).
Google Scholar
Wright, I. J. et al. The worldwide leaf economics spectrum. Nature 428, 821–827 (2004).
Google Scholar
Ishida, A. et al. Coordination between leaf and stem traits related to leaf carbon gain and hydraulics across 32 drought-tolerant angiosperms. Oecologica 156, 193–202 (2008).
Google Scholar
He, P. et al. Leaf mechanical strength and photosynthetic capacity wary independently across 57 subtropical forest species with contrasting light requirements. New Phytol. 223, 607–618 (2019).
Google Scholar
Yamashita, N., Koike, N. & Ishida, A. Leaf ontogenetic dependence of light acclimation in invasive and native subtropical trees of different successional status. Plant Cell Environ. 25, 1341–1356 (2002).
Google Scholar
McDowell, N. et al. Mechanisms of plant survival and mortality during drought: Why do some plants survive while others succumb to drought?. New Phytol. 178, 719–739 (2008).
Google Scholar
Sala, A., Piper, F. & Hoch, G. Physiological mechanisms of drought-induced tree mortality are far from being resolved. New Phytol. 186, 274–281 (2010).
Google Scholar
O’Brien, M. J., Leuzinger, S., Philipson, C. D., Tay, J. & Hector, A. Drought survival of tropical tree seedlings enhanced by non-structural carbohydrate levels. Nat. Clim. Change 4, 710–714 (2014).
Google Scholar
Saiki, S.-T., Ishida, A., Yoshimura, K. & Yazaki, K. Physiological mechanisms of drought-induced tree die-off in relation to carbon, hydraulic and respiratory stress in a drought-tolerant woody plant. Sci. Rep. 7, 2995. https://doi.org/10.1038/s41598-017-03162-5 (2017).
Google Scholar
Kono, Y. et al. Initial hydraulic failure followed by late-stage carbon starvation leads to drought-induced death in the tree Trema orientalis. Commun. Biol. 2, 8. https://doi.org/10.1038/s42003-018-0256-7 (2019).
Google Scholar
Ebbert, V., Adams, W. W. III., Mattoo, A. K., Sokolenko, A. & Demming-Adams, B. Up-regulation of a photosystem II core protein phosphatase inhibitor and sustained D1 phosphorylation in zeaxanthin-retaining, photoinhibited needles of overwintering Douglas fir. Plant Cell Environ. 28, 232–240 (2005).
Google Scholar
Harayama, H., Ikeda, T., Ishida, A. & Yamamoto, S. I. Seasonal variations in water relations in current-year leaves of evergreen trees with delayed greening. Tree Physiol. 26, 1025–1033 (2006).
Google Scholar
Yasumura, Y. & Ishida, A. Temporal variation in leaf nitrogen partitioning of a broad-leaved evergreen tree, Quercus myrsinaefolia. J. Plant Res. 124, 115–123 (2011).
Google Scholar
Fowler, S. & Thomashow, M. F. Arabidopsis trancriptome profiling indicates that multiple regulatory pathways are activated during cold acclimation in addition in to the CBF cold response pathway. Plant Cell 14, 1675–1690 (2002).
Google Scholar
Oono, Y. et al. Monitoring expression profiles of Arabidopsis genes during cold acclimation and deacclimation using DNA microarrays. Funct. Integr. Genom. 6, 212–234 (2006).
Google Scholar
Nakaminami, K. et al. Analysis of differential expression patterns of mRNA and protein during acclimation and de-acclimation in Arabidopsis. Mol. Cell. Proteom. 13, 3602–3611 (2014).
Google Scholar
Wang, H. et al. Acclimation of leaf respiration consistent with optimal photosynthetic capacity. Glob. Chang Biol. 26, 2573–2583 (2020).
Google Scholar
Maseyk, K., Grünzweig, J. M., Rotenberg, E. & Yakir, D. Respiration acclimation contributes to high carbon-use efficiency in a seasonally dry pine forest. Glob. Change Biol. 14, 1553–1567 (2008).
Google Scholar
Jarvi, M. P. & Burton, A. J. Acclimation and soil moisture constrain sugar maple root respiration in experimentally warmed soil. Tree Physiol. 33, 949–959 (2013).
Google Scholar
Smith, N. G., Li, G. & Dukes, J. S. Short-term thermal acclimation of dark respiration is greater non-photosynthetic than in photosynthetic tissues. AoBP Plants 11, 1–9 (2019).
Google Scholar
Bennett, J. R. & Scotland, R. E. A revision of Strobilanthes (Acanthaceae) in Java. Kew. Bull. 58, 1–82 (2003).
Google Scholar
Wood, J. R. I. & Scotland, R. W. New and little-known species of Strobitlanthes (Acanthaceae) from India and South East Asia. Kew. Bull. 64, 3–47 (2009).
Google Scholar
Vongkamjan, S. & Sampson, F. B. Phenology, seed germination and some vegetative features of Strobilanthes fragrans (Acanthaceae), a recently described unusual species, found only in a single Forest Park in Thailand. Thai Forest Bull. Bot. 44, 6–10 (2016).
Google Scholar
Tsukaya, H., Kakishima, S., Hidayat, A., Murata, J. & Okada, H. Flowering phenology of the nine-year plant, Strobilanthes cernua (Acanthaceae). Tropics 20, 79–85 (2011).
Google Scholar
Sharma, M. V., Kuriakose, G. & Shivanna, K. R. Reproductive strategies of Strobilanthes kunthianus, an endemic, semelparous species in southern Western Ghats, India. Bot. J. Linn. Soc. 157, 155–163 (2008).
Google Scholar
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