Interspecific competition in natural plant communities is highly dependent
on nutrient availability. At high levels of nutrient availability, competit
ion is mainly for light, As light is a unidirectional resource, high-nutrie
nt habitats are dominated by fast-growing perennials with a tall stature an
d a rather uniform vertical distribution of leaf area. Moreover, these spec
ies have high turnover rates of leaves and roots and a high morphological p
lasticity during the differentiation of leaves. There is less consensus, ho
wever, about the importance and intensity of interspecific competition in n
utrient-poor environments. It is argued that selection in nutrient-poor hab
itats is not necessarily on a high competitive ability for nutrients and a
high growth rate, but rather on traits which reduce nutrient losses (low ti
ssue nutrient concentrations, slow tissue turnover rates, high nutrient res
orption efficiency), Due to evolutionary trade-offs plants can not maximize
both growth rate and nutrient retention. Thus, the low growth rate of spec
ies from nutrient-poor habitats should be considered as the consequence of
nutrient retention rather than as a feature on which direct selection takes
place. The contrasting traits of species from nutrient-poor and nutrient-r
ich habitats mutually exclude them from each others' habitats. Moreover, th
ese traits have severe consequences for litter decomposability and thereby
also for nutrient cycling. This leads both in nutrient-poor and nutrient-ri
ch habitats to a positive feedback between plant species dominance and nutr
ient availability, thereby promoting ecosystem stability.