2022
DOI: 10.1016/j.envexpbot.2022.104787
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Disentangling carbon uptake and allocation in the stems of a spruce forest

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Cited by 25 publications
(18 citation statements)
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“…(2018) presented that the culmination of radial increment for Norway spruce usually occurs around the beginning-middle of June. Krejza et al. (2022) in a study aimed on carbon uptake and allocation in mature Norway spruce monoculture (located 30 km from our study location), showed the radial growth onset on old Norway spruce in the middle of May (128 DOY), ends in the beginning of September (249 DOY) with the highest rates of daily increment between the second half of May till the beginning of August (139 to 214 DOY), which agrees with our study.…”
Section: Discussionsupporting
confidence: 92%
“…(2018) presented that the culmination of radial increment for Norway spruce usually occurs around the beginning-middle of June. Krejza et al. (2022) in a study aimed on carbon uptake and allocation in mature Norway spruce monoculture (located 30 km from our study location), showed the radial growth onset on old Norway spruce in the middle of May (128 DOY), ends in the beginning of September (249 DOY) with the highest rates of daily increment between the second half of May till the beginning of August (139 to 214 DOY), which agrees with our study.…”
Section: Discussionsupporting
confidence: 92%
“…Trees consequently grow mainly at night. Growth processes clearly come to a halt before the onset of stomatal closure (VPD > 0.8 kPa) and the photosynthetic output coupled to it, which was recently confirmed by Krejza et al (2022). However, if the soil water potential sinks too low during a dry period, even high air humidity (low VPD) can no longer initiate growth.…”
Section: Introductionmentioning
confidence: 70%
“…In addition, drought conditions often trigger stomatal down-regulation entailing a rise in leaf temperature due to reduced transpirational cooling (Leuzinger and Körner, 2007;Scherrer et al, 2011). Commonly, drought-related reductions in g s do not (rapidly) result in carbohydrate depletion but often rather in an increase in non-structural carbohydrates due to diminished sink strength since structural sinks are far more sensitive to turgor loss than photosynthesis (Körner, 2019;Krejza et al, 2022). Even under curtailed photosynthate supply, the maintenance of non-structural carbohydrate levels has been shown to take precedence over carbon allocation to growth across a variety of woody species (Weber et al, 2019).…”
Section: Radial Stem Incrementmentioning
confidence: 99%
“…lack of considering inter-annual variability of wood anatomy (Björklund et al 2017), which can lead to relevant biases (Cuny et al 2015, Pretzsch et al 2018, Vannoppen et al 2018. Other methods to assess tree growth, such as stem circumference increment (Delpierre et al 2016) and xylogenesis (Krejza et al 2022) monitoring, are more temporally detailed and provide information on intra-annual wood formation processes and phenology, but lack the temporal extent of tree rings necessary to assess how inter-annual variability of C fluxes affects tree radial growth.…”
Section: Introductionmentioning
confidence: 99%
“…When wood anatomical variations are assessed at the intra-ring level, intra-seasonal climate influence on tree radial growth can be retrieved, overcoming the typical annual resolution of TRW analysis (Castagneri et al 2017, Belokopytova et al 2019, Pérez-de-Lis et al 2022. Since both ecosystem productivity and wood formation patterns vary considerably over the growing season, and show different sensitivity to seasonal climate (Deslauriers et al 2017, Xu et al 2020, Krejza et al 2022, long time-series analysis at intra-annual scale could disclose the complex relationships between environmental variability, C fluxes and biomass accumulation in wood which are obscured by annually resolved analyses.…”
Section: Introductionmentioning
confidence: 99%