2013
DOI: 10.1007/s00468-013-0919-4
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Instantaneously measured traits may detect non-plastic ecophysiological performances in response to drought, explaining distributions of Styrax species in the Cerrado

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Cited by 11 publications
(5 citation statements)
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“…These adjustment strategies of C. langsdorffii found in Cerrado physiognomies corroborate data by Veiga and Habermann (2013), who suggest that species in this ecosystem exhibit photoprotection performance under water stress. Thus, the capacity of making diurnal adjustments in photochemical and non-photochemical processes in order to overcome photoinhibitory threats would play a central role in the understanding of photosynthesis acclimation in seasonal environments like in Cerrado, regardless of the prevailing irradiance levels and degree of stomata closure (Franco and Lüttge, 2002).…”
Section: Discussionsupporting
confidence: 88%
“…These adjustment strategies of C. langsdorffii found in Cerrado physiognomies corroborate data by Veiga and Habermann (2013), who suggest that species in this ecosystem exhibit photoprotection performance under water stress. Thus, the capacity of making diurnal adjustments in photochemical and non-photochemical processes in order to overcome photoinhibitory threats would play a central role in the understanding of photosynthesis acclimation in seasonal environments like in Cerrado, regardless of the prevailing irradiance levels and degree of stomata closure (Franco and Lüttge, 2002).…”
Section: Discussionsupporting
confidence: 88%
“…Cerrado conservation has been a major challenge due to lack of scientific information regarding the plant responses to environmental stresses that occur in the different physiognomies of this biome. Studies addressing native species have been carried out in greenhouse and in loco (Veiga and Habermann, 2013;Dalmolin et al, 2015;Garcia et al, 2015). However, little is known about the effects of drought on woody species from Cerrado.…”
Section: Introductionmentioning
confidence: 99%
“…To estimate the photoprotective role of anthocyanins, we measured chlorophyll a fluorescence and calculated the fraction of absorbed light used in photochemical activity [ P = (Fm′ − Fs)/Fm′], which is equivalent to the effective quantum yield of photosystem II (ΦPSII), the heat dissipation in the light‐gathering pigment antenna, which collects light and transfers the energy to the reaction center complex ( D = 1 – Fv′/Fm′) and the heat dissipation in reaction centers of photosystem II, PSII [ E = (1 – qP)(Fv′/Fm′)] according to da Veiga and Habermann (2013). We used saturating light pulses of 7000 µmol photons·m −2 ·s −1 for 0.7 s. For these equations, Fv′ is the variable fluorescence between the maximal (Fm′) and minimal (Fo′) fluorescence of light‐adapted fruits, and Fs is the steady‐state fluorescence of light‐adapted fruits.…”
Section: Methodsmentioning
confidence: 99%