Forest succession suppressed by an introduced plant-fungal symbiosis.

Microbial symbionts can affect plant nutrition, defensive chemistry, and biodiversity. Here we test the hypothesis that symbionts alter the speed and direction of plant succession in communities that are shifting from grasslands to forests. A widespread C3 grass introduced to the United States, Lolium arundinaceum (tall fescue), hosts a fungal endophyte that is toxic to herbivores.

Herbivores cause a rapid increase in hereditary symbiosis and alter plant community composition.

Microbial symbioses are ubiquitous in nature. Hereditary symbionts warrant particular attention because of their direct effects on the evolutionary potential of their hosts. In plants, hereditary fungal endophytes can increase the competitive ability, drought tolerance, and herbivore resistance of their host, although it is unclear whether or how these ecological benefits may alter the dynamics of the endophyte symbiosis over time.

Impacts of a native root-rotting pathogen on successional development of old-growth Douglas fir forests.

Because Pseudotsuga menziesii (Douglas fir), an early seral dominant in western Oregon forests, is particularly susceptible to the pathogenic root rot caused by the fungus Phellinus weirii, it was hypothesized that successional development in affected forests would be accelerated. The basal area of late successional tree species and common shrubs were compared inside and outside Phellinus weirii"infection centers". Future successional impacts indirectly caused by disease presence were assessed by comparing the abundance of regenerating tree species inside and outside of these centers.