2014
DOI: 10.1111/gcb.12781
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Acclimation of photosynthetic temperature optima of temperate and boreal tree species in response to experimental forest warming

Abstract: Rising temperatures caused by climate change could negatively alter plant ecosystems if temperatures exceed optimal temperatures for carbon gain. Such changes may threaten temperature‐sensitive species, causing local extinctions and range migrations. This study examined the optimal temperature of net photosynthesis (Topt) of two boreal and four temperate deciduous tree species grown in the field in northern Minnesota, United States under two contrasting temperature regimes. We hypothesized that Topt would be h… Show more

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Cited by 118 publications
(113 citation statements)
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“…Temperate deciduous trees usually increase T opt in response to warming (Sendall et al . ), which would correspond with our observation of increasing D opt with increasing VPD in all species (Fig. ).…”
Section: Discussionsupporting
confidence: 91%
“…Temperate deciduous trees usually increase T opt in response to warming (Sendall et al . ), which would correspond with our observation of increasing D opt with increasing VPD in all species (Fig. ).…”
Section: Discussionsupporting
confidence: 91%
“…Similarly, the "optimum temperature for photosynthesis" (PSNTOPT) is found to be much lower for boreal (FI-Hyy, FI-Sod, in average 8.74 °C) than for temperate forest (NL-Loo, BE-Bra). This is in agreement with field experiments where the link between photosynthetic response potentials and prevailing growing season temperatures had been demonstrated [120]. The differentiation of site-calibrated parameters in this study indicates the degree of acclimation of trees to specific environmental conditions.…”
Section: Site-specific Versus Multi-site (Species-specific) Parametrisupporting
confidence: 91%
“…A number of previous studies have demonstrated short‐term acclimation of Rubisco kinetics to growth temperature (Medlyn et al ., ; Yamori et al ., ; Kattge & Knorr, ; Lin et al ., ; Yamaguchi et al ., ; Smith & Dukes, ; Crous et al ., ), although the sensitivities of the responses varied. In addition, studies that have compared the acclimation capacity of multiple species in common growth temperatures have shown similar direction and magnitude of short‐term temperature acclimation of T optA (Berry & Björkman, ; Sendall et al ., ) and Rubisco kinetics (Lin et al ., ; Smith & Dukes, ) across species irrespective of their climate of origin. Therefore, we argue that the capacity of species to adjust their photosynthetic biochemistry to temporal variations in growth temperature provides a fitness advantage over that of local climatic adaptation of T optA and its related mechanisms, by enabling species to optimize C balance in their current habitat (Hikosaka et al ., ).…”
Section: Discussionmentioning
confidence: 99%
“…For curves where the first point was not measured at ambient CO 2 concentration, we extracted the A net value at the measured sample CO 2 concentration falling between 300 and 400 ppm. We estimated the temperature optimum for A net , T optA , by fitting a widely used model of instantaneous photosynthetic temperature response (Gunderson et al ., ; Crous et al ., ; Sendall et al ., ; Vårhammar et al ., ) 1) to the net photosynthesis measurements. The model is a quadratic equation, expressed as: Anormalnet=Anormaloptb(TTnormaloptA)2,where A net is the net photosynthetic rate (μmol m −2 s −1 ) at a given leaf temperature, T (°C), T optA is the temperature optimum for photosynthesis (°C), A opt is the net photosynthetic rate at T optA , and the parameter b (unitless) describes the degree of curvature of the relationship.…”
Section: Methodsmentioning
confidence: 99%