Does lower water availability limit stem CO2 efflux of oak and hornbeam coppices?

Recent changes in water availability can be crucial for the development, growth and carbon budget of forests. Therefore, our aim was to determine the effect of reduced throughfall and severe summer drought on stem CO2 efflux as a function of temperature and stem increment. Stem CO2 efflux was measured using the chamber method on oak and hornbeam under four treatments: coppice, thinned coppice, and both coppice and thinned coppice with 30 %-reduced throughfall. The first year of the experiment had favourable soil water availability and the second year was characterized by a dry summer. While reduced throughfall had no effect on stem CO2 efflux, the summer drought decreased efflux by 43-81 % during July and August. The stem CO2 efflux was reduced less severely (by 13-40 %) in September when the drought persisted but the stem increment was already negligible. The stem increment was also strongly affected by the drought, which was reflected in its paired relationship with stem CO2 efflux over the two experimental years. The study showed that summer dry periods significantly and rapidly reduce stem CO2 efflux, whereas a constant 30 % rainfall reduction needs probably a longer time to affect stem properties, and indirectly stem CO2 efflux.

Response of beech and fir to different light intensities along the Carpathian and Dinaric Mountains.

Predicting global change mitigations based on environmental variables, like temperature and water availability, although yielding insightful hypothesis still lacks the integration of environmental responses. Physiological limits should be assessed to obtain a complete representation of a species' fundamental niche. Detailed ecophysiological studies on the response of trees along the latitudinal gradient are rare. They could shed light on the behaviour under different light intensities and other studied traits. The forests of the Dinaric Mountains and the Carpathians represent the largest contiguous forest complexes in south-eastern Europe. In uneven-aged Carpathian (8 plots) and Dinaric Mountain (11 plots) forests, net assimilation (Amax) and maximum quantum yield (Φ) were measured for beech and fir in three predefined light intensity categories according to the indirect site factor (ISF%) obtained by the analysis of hemispherical photographs in managed and old growth forests, all located above 800 m a.s.l. The measurements were carried out under fixed environmental conditions in each light category per plot for three consecutive years. Data from the last 50-year average period from the CRU TS 4.01 dataset were used for the comparison between Amax, Φ, and climate. The highest Φ for beech were observed in the central part of the Dinaric Mountains and in the south westernmost and northwesternmost part of the Carpathians for both beech and fir, while they were highest for fir in the Dinaric Mountains in the northwesternmost part of the study area. The Φ-value of beech decreased in both complexes with increasing mean annual temperature and was highest in the open landscape. For fir in the Carpathians, Φ decreased with increasing mean annual temperature, while in the Dinaric Mountains it increased with higher temperature and showed a more scattered response compared to the Carpathians. Short-term ecophysiological responses of beech and fir were consistent to long-term radial growth observations observed on same locations. The results may provide a basis and an indication of the future response of two tree species in their biogeographical range to climate change in terms of competitiveness, existence and consequently forest management decisions.

Seasonally varying relationship between stem respiration, increment and carbon allocation of Norway spruce trees.

Stem respiration is an important component of an ecosystem's carbon budget. Beside environmental factors, it depends highly on tree energy demands for stem growth. Determination of the relationship between stem growth and stem respiration would help to reveal the response of stem respiration to changing climate, which is expected to substantially affect tree growth. Common measurement of stem radial increment does not record all aspects of stem growth processes, especially those connected with cell wall thickening; therefore, the relationship between stem respiration and stem radial increment may vary depending on the wood cell growth differentiation phase. This study presents results from measurements of stem respiration and increment carried out for seven growing seasons in a young Norway spruce forest. Moreover, rates of carbon allocation to stems were modeled for these years. Stem respiration was divided into maintenance (Rm) and growth respiration (Rg) based upon the mature tissue method. There was a close relationship between Rg and daily stem radial increment (dSRI), and this relationship differed before and after dSRI seasonal maximum, which was around 19 June. Before this date, Rg increased exponentially with dSRI, while after this date logarithmically. This is a result of later maxima of Rg and its slower decrease when compared with dSRI, which is connected with energy demands for cell wall thickening. Rg reached a maxima at the end of June or in July. The maximum of carbon allocation to stem peaked in late summer, when Rg mostly tended to decrease. The overall contribution of Rg to stem CO2 efflux amounted to 46.9% for the growing period from May to September and 38.2% for the year as a whole. This study shows that further deeper analysis of in situ stem growth and stem respiration dynamics is greatly needed, especially with a focus on wood formation on a cell level.

Variability of stem CO2 efflux response to temperature over the diel period.

This study presents results from continuous measurements of stem CO2 efflux carried out for seven growing seasons in a young Norway spruce forest. The objective of the study was to determine differences in temperature sensitivity of stem CO2 efflux (Q10) during night (when sap flow is zero or nearly zero), during early afternoon (when the maximum rate of sap flow occurs) and during two transition periods between the aforementioned periods. The highest Q10 was recorded during the period of zero sap flow, while the lowest Q10 was observed in period of the highest sap flow. Calculating Q10 using only data from the period of zero sap flow resulted in a Q10 that was higher by as much as 19% compared with Q10 calculated using 24 h data. On the other hand, basing the calculation on data from the period of the highest sap flow yielded 5.6% lower Q10 than if 24 h data were used. Considering that change in CO2 efflux lagged in time behind changing stem temperature, there was only a small effect on calculated Q10 for periods with zero and the highest sap flow. A larger effect of the time lag (by as much as 15%) was observed for the two transition periods. Stem CO2 efflux was modelled based on the night CO2 efflux response to temperature. This model had a tendency to overestimate CO2 efflux during daytime, thus indicating potential daytime depression of stem CO2 efflux compared with the values predicated on the basis of temperature caused by CO2 transport upward in the sap flow. This view was supported by our results inasmuch as the overestimation grew with sap flow that was modelled on the basis of photosynthetically active radiation and vapour pressure deficit.

Variability in temperature dependence of stem CO2 efflux from Norway spruce trees.

This study presents results from continuous measurements of stem CO2 efflux carried out for seven experimental seasons (from May to October) in a young Norway spruce forest. The objectives of the study were to determine variability in the response of stem CO2 efflux to stem temperature over the season and to observe differences in the calculated relationship between stem temperature and CO2 efflux based on full growing season data or on data divided into periods according to stem growth rate. Temperature sensitivity of stem CO2 efflux (Q10) calculated for the established periods ranged between 1.61 and 3.46 and varied over the season, with the lowest values occurring in July and August. Q10 calculated using data from the full growing seasons ranged between 2.30 and 2.94 and was often significantly higher than Q10 calculated for the individual periods. Temperature-normalized stem CO2 efflux (R10) determined using Q10 from growing season data was overestimated when the temperature was below 10 °C and underestimated when the temperature was above 10 °C, compared with R10 calculated using Q10 established for the individual periods. The differences in daily mean R10 calculated by these two approaches ranged between -0.9 and 0.2 µmol CO2 m-2 s-1. The results of this study confirm that long periods for determining the temperature dependence of stem CO2 efflux encompass different statuses of the wood (especially in relation to stem growth). This may cause bias in models using this relationship for estimating stem CO2 efflux as a function of temperature.