On the Ecology of Mountainous Forests in a Changing Climate: A ...
On the Ecology of Mountainous Forests in a Changing Climate: A ...
On the Ecology of Mountainous Forests in a Changing Climate: A ...
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Behaviour <strong>of</strong> FORCLIM along a transect <strong>in</strong> <strong>the</strong> European Alps 103<br />
The results obta<strong>in</strong>ed from FORCLIM-P at <strong>the</strong> site Sion do not correspond to phytosociological<br />
expectations (Fig. 4.7): Although this site is very xeric, an extremely high biomass<br />
is atta<strong>in</strong>ed; while <strong>the</strong> occurrence <strong>of</strong> Q. robur is plausible (Ellenberg 1986), <strong>the</strong> codom<strong>in</strong>ance<br />
<strong>of</strong> chestnut (Castanea sativa) may be questionable, and <strong>the</strong> considerable biomass<br />
<strong>of</strong> yew (Taxus baccata) is unrealistic as well.<br />
The litter production simulated by FORCLIM-P is summarized <strong>in</strong> Tab. 4.4. In coniferous<br />
forests, leaf litter <strong>of</strong> low quality is produced (uFL 3 ), whereas deciduous forests are characterized<br />
by more easily degradable leaf litter (uFL 2 ). There is some literature data to<br />
evaluate <strong>the</strong> simulated pattern <strong>of</strong> total aboveground litterfall: For boreal forests (comparable<br />
to <strong>the</strong> sites Davos and Bever), Ajtay et al. (1979) give 5.5–6 t·ha -1·yr-1 , while <strong>the</strong>ir<br />
value for temperate forests (Bern, Sion, Locarno) is 8.5 t·ha -1·yr-1 ; <strong>the</strong> rates simulated<br />
by FORCLIM-P are slightly lower. <strong>On</strong> <strong>the</strong> o<strong>the</strong>r hand, Cox et al. (1978) found only<br />
3.3 t·ha -1·yr-1 <strong>in</strong> a Liriodendron forest <strong>in</strong> Tennessee. For coarse woody debris (correspond<strong>in</strong>g<br />
roughly to uWL), Harmon et al. (1986) list a range <strong>of</strong> 0.17–7 t·ha -1·yr-1 <strong>in</strong><br />
coniferous forests, and up to 14.5 t ha -1·yr-1 <strong>in</strong> deciduous forests. The simulated aboveground<br />
litter production (Tab. 4.4) agrees with <strong>the</strong> range <strong>of</strong> data from <strong>the</strong>se sources (cf.<br />
also Vogt et al. 1986).<br />
4.3.2 FORCLIM-E/P<br />
In this model setup, <strong>the</strong> abiotic environment is stochastic; thus, it is not restricted to<br />
average conditions but <strong>in</strong>cludes some <strong>of</strong> <strong>the</strong> natural variability <strong>of</strong> <strong>the</strong> wea<strong>the</strong>r and <strong>the</strong><br />
habitat. As <strong>in</strong> section 4.3.1, available nitrogen is kept constant at 100 kg/ha. The results<br />
<strong>of</strong> <strong>the</strong>se simulations are shown <strong>in</strong> Fig. 4.8 & 4.9.<br />
At <strong>the</strong> site Bever (Fig. 4.8), <strong>the</strong> spruce forest simulated by FORCLIM-P (Fig. 4.6) is replaced<br />
by <strong>the</strong> Larici-P<strong>in</strong>etum cembrae, where P. cembra dom<strong>in</strong>ates (Ellenberg & Klötzli<br />
1972). Picea excelsa is not competitive any more due to <strong>the</strong> occurrence <strong>of</strong> summer<br />
droughts. <strong>On</strong> nor<strong>the</strong>rn slopes at Bever (Fig. 4.12), a larch-spruce forest is simulated,<br />
correspond<strong>in</strong>g to <strong>the</strong> pattern observed <strong>in</strong> <strong>the</strong> area (Ellenberg & Klötzli 1972).<br />
The forest simulated at <strong>the</strong> site Davos (Fig. 4.8) does not differ much from <strong>the</strong> one simulated<br />
by FORCLIM-P (Fig. 4.6); it still belongs to <strong>the</strong> Larici-Piceetum (Ellenberg &<br />
Klötzli 1972). Silver fir (Abies alba) occurs now because w<strong>in</strong>ter temperature <strong>in</strong> some<br />
years is high enough to enable establishment <strong>of</strong> <strong>the</strong> species. Its presence at elevations