Rust fungi and global change.

Rust fungi are important components of ecological communities and in ecosystem function. Their unique life strategies as biotrophic pathogens with complicated life cycles could make them vulnerable to global environmental change. While there are gaps in our knowledge, especially in natural plant­rust systems, this review of the exposure of rust fungi to global change parameters revealed that some host­rust relationships would decline under predicted environmental change scenarios, whereas others would either remain unchanged or become more prevalent. Notably, some graminicolous rusts are negatively affected by higher temperatures and increased concentrations of atmospheric CO2. An increase of atmospheric O3 appears to favour rust diseases on trees but not those on grasses. Combined effects of CO2 and O3 are intermediary. The most important global drivers for the geographical and host plant range expansion and prevalence of rusts, however, are global plant trade, host plant genetic homogenization and the regular occurrence of conducive environmental conditions, especially the availability of moisture. However, while rusts thrive in high-humidity environments, they can also survive in desert habitats, and as a group their environmental tolerance is large, with no conclusive change in their overall prevalence predictable to date.

Molecular evidence indicates that subarctic willow communities in Scotland support a diversity of host-associated Melampsora rust taxa.

Rare and threatened subarctic willow scrub communities in the UK are the subject of ongoing conservation programmes, yet little is known about the diversity of fungal taxa that they support. Isolates of the rust genus Melampsora were sampled from 112 leaves of eight subarctic willow (Salix) taxa and their hybrids from twelve sites in the UK. In order to determine the number of Melampsora taxa present in the samples, isolates were sequenced for the Internal Transcribed Spacer (ITS) region of rDNA and data were subject to phylogenetic analysis. Maximum likelihood and Bayesian analysis indicated that the isolates fell into three strongly supported host-associated clades. Clade I contained only isolates from Salix herbacea and was distinguished morphologically by dense urediniospore echinulation and thin cell walls. Clade II contained isolates from Salix arbuscula and Salix reticulata only. These could not be distinguished morphologically from isolates in Clade III which were found on Salix lapponum, Salix myrsinites, Salix myrsinifolia, Salix aurita, Salix lanata, and their hybrids. Clade II was most distinct in ITS sequence, differing by 50 bases from Clades I and III, while the latter clades differed in sequence by only 24 bases on average. Clades I and III are likely to represent the previously recognised taxa Melampsora alpina Juel 1894 and Melampsora epitea Thüm. 1879 respectively, but Clade II has not apparently been described before. Significant differences in the intensity of infection by isolates of Clade III were found among different Salix species at a single site, suggesting either differences in resistance among Salix taxa, or the presence of further cryptic taxa within Clade III. The study illustrates the power of molecular phylogenetic analysis to reveal cryptic biodiversity within Melampsora, and suggests that conserving Salix host diversity within subarctic willow communities will ensure that a diversity of associated Melampsora taxa is maintained.