Influence of Ozone and Drought on Tree Growth under Field Conditions in a 22 Year Time Series
(2022)
Studying the effect of surface ozone (O3) and water stress on tree growth is important for planning sustainable forest management and forest ecology. In the present study, a 22-year long time series (1998–2019) on basal area increment (BAI) and fructification severity of European beech (Fagus sylvatica L.) and Norway spruce (Picea abies (L.) H.Karst.) at five forest sites in Western Germany (Rhineland Palatinate) was investigated to evaluate how it correlates with drought and stomatal O3 fluxes (PODY) with an hourly threshold of uptake (Y) to represent the detoxification capacity of trees (POD1, with Y = 1 nmol O3 m−2 s−1). Between 1998 and 2019, POD1 declined over time by on average 0.31 mmol m−2 year−1. The BAI showed no significant trend at all sites, except in Leisel where a slight decline was observed over time (−0.37 cm2 per year, p < 0.05). A random forest analysis showed that the soil water content and daytime O3 mean concentration were the best predictors of BAI at all sites. The highest mean score of fructification was observed during the dry years, while low level or no fructification was observed in most humid years. Combined effects of drought and O3 pollution mostly influence tree growth decline for European beech and Norway spruce.
Using a dendrochronological approach, we determined the resistance, recovery and resilience of the radial stem increment towards episodes of growth decline, and the accompanying variation of 13C discrimination against atmospheric CO2 (Δ13C) in tree rings of two palaeotropical pine species. These species co-occur in the mountain ranges of south–central Vietnam (1500–1600 m a.s.l.), but differ largely in their areas of distribution (Pinus kesiya from northeast India to the Philippines; P. dalatensis only in south and central Vietnam and in some isolated populations in Laos). For P. dalatensis, a robust growth chronology covering the past 290 years could be set up for the first time in the study region. For P. kesiya, the 140-year chronology constructed was the longest that could be established to date in that region for this species. In the first 40 years of the trees’ lives, the stem diameter increment was significantly larger in P. kesiya, but levelled off and even decreased after 100 years, whereas P. dalatensis exhibited a continuous growth up to an age of almost 300 years. Tree-ring growth of P. kesiya was negatively related to temperature in the wet months and season of the current year and in October (humid transition period) of the preceding year and to precipitation in August (monsoon season), but positively to precipitation in December (dry season) of the current year. The P. dalatensis chronologies exhibited no significant correlation with temperature or precipitation. Negative correlations between BAI and Δ13C indicate a lack of growth impairment by drought in both species. Regression analyses revealed a lower resilience of P. dalatensis upon episodes of growth decline compared to P. kesiya, but, contrary to our hypothesis, mean values of the three sensitivity parameters did not differ significantly between these species. Nevertheless, the vigorous growth of P. kesiya, which does not fall behind that of P. dalatensis even at the margin of its distribution area under below-optimum edaphic conditions, is indicative of a relatively high plasticity of this species towards environmental factors compared to P. dalatensis, which, in tendency, is less resilient upon environmental stress even in the “core” region of its occurrence.