Michael A. Castellano

Multiple origins of sequestrate fungi related to Cortinarius (Cortinariaceae).

The aim of the present study was to investigate the phylogeny and evolution of sequestrate fungi (with gastroid or partially exposed basidiomes) in relation to their gilled relatives from the Cortinariaceae (Basidiomycetes). Phylogenetic analyses of 151 ITS sequences from 77 gilled species and 37 sequestrate taxa were performed using maximum parsimony and maximum likelihood methods. Results show that sequestrate basidiome forms occur in all three major ectomycorrhizal lineages of Cortinariaceae: the clades Cortinarius, Hebeloma/Hymenogaster/Naucoria, and Descolea. However, these forms do not appear within the saprobic outgroup Gymnopilus, indicating multiple origins of sequestrate forms from ectomycorrhizal ancestors. Additionally, within the Cortinarius clade sequestrate forms have multiple origins: emergent Cortinarius spp., Thaxterogaster, Quadrispora, Protoglossum, and two Hymenogaster spp. (H. remyi, H. sublilacinus) share common ancestors with Cortinarius spp., but these sequestrate genera are not closely related to each other (with exception of Thaxterogaster and Quadrispora). Hymenogaster sensu stricto, Setchelliogaster, and Descomyces were placed in the two other major clades. Thus, sequestrate taxa evolved independently many times within brown-spored Agaricales. Furthermore, emergent, secotioid, and gastroid forms have evolved independently from each other, and so are not necessarily intermediate forms. After their establishment, these apparently morphologically stable taxa show a tendency to radiate.

Ectomycorrhizal fungi in Eucalyptus and Pinus plantations in southern Brazil.

The occurrence of ectomycorrhizal fungi (EMF) was assessed during 4 seasons (1 yr) in 10 plantations of Eucalyptus spp. and Pinus spp. in the state of Santa Catarina, southern Brazil. Forty-nine presumed EMF taxa representing 9 orders and 12 families were identified, including epigeous and se- questrate species. Many are first reports for South America, and 3 are new species, Chondrogaster au- gustisporus, Descomyces giachinii, and Scleroderma bougheri. Fruiting patterns of EMF differed by host, and host specificity was apparent for some. Laccaria and Scleroderma were the prevalent genera through- out the year in both plantation types. The results of the study show that species richness of EMF in Brazil is higher than previously demonstrated.

Biogeography of Hysterangiales (Phallomycetidae, Basidiomycota)

To understand the biogeography of truffle-like fungi, DNA sequences were analysed from representative taxa of Hysterangiales. Multigene phylogenies and the results of ancestral area reconstructions are consistent with the hypothesis of an Australian, or eastern Gondwanan, origin of Hysterangiales with subsequent range expansions to the Northern Hemisphere. However, neither Northern Hemisphere nor Southern Hemisphere taxa formed a monophyletic group, which is in conflict with a strictly vicariant scenario. Therefore, the occurrence and importance of long-distance dispersal could not be rejected. Although a pre-Gondwanan origin of Hysterangiales remains as a possibility, this hypothesis requires that Hysterangiales exist prior to the origin of the currently recognized ectomycorrhizal plants, as well as the arrival of mycophagous animals in Australia. This also requires that a basal paraphyletic assemblage represents parallel evolution of the ectomycorrhizal symbiosis, or that Hysterangiales was mycorrhizal with members of the extinct flora of Gondwana. Regardless, models for both ancient and more recent origins of Hysterangiales are consistent with truffle-like fungi being capable of transoceanic dispersal.

Outplanting performance of mycorrhizal inoculated seedlings

Many references and unpublished data on outplanting performance of mycorrhizal inoculated seedlings are summarized. Two comprehensive tables are presented, one by fungus and one by host plant, as ready references to the literature for reforestation workers and scientists studying the effects of mycorrhizal inoculation on seedling performance after out-planting in the field. Pisolithus tinctorius is the most extensively studied mycorrhizal fungus, and Pinus spp. have received the most attention for host plants. A more thorough investigation is needed of other fungus-host combinations to better predict when and where mycorrhizal inoculation is beneficial to seedling outplanting performance.

Diversity, ecology, and conservation of truffle fungi in forests of the Pacific Northwest

Forests of the Pacific Northwest have been an epicenter for the evolution of truffle fungi with over 350 truffle species and 55 genera currently identified. Truffle fungi develop their reproductive fruit-bodies typically belowground, so they are harder to find and study than mushrooms that fruit aboveground. Nevertheless, over the last five decades, the Corvallis Forest Mycology program of the Pacific Northwest Research Station has amassed unprecedented knowledge on the diversity and ecology of truffles in the region. Truffle fungi form mycorrhizal symbioses that benefit the growth and survival of many tree and understory plants. Truffle fruit-bodies serve as a major food souce for many forest-dwelling mammals. A few truffle species are commercially harvested for gourmet consumption in regional restaurants. This publication explores the biology and ecology of truffle fungi in the Pacific Northwest, their importance in forest ecosystems, and effects of various silvicultural practices on sustaining truffle populations. General management principles and considerations to sustain this valuable fungal resource are provided.

Fungal Conservation: Conservation and management of forest fungi in the Pacific Northwestern United States: an integrated ecosystem approach

The vast forests of the Pacific Northwest region of the United States, an area outlined by the states of Oregon, Washington, and Idaho, are well known for their rich diversity of macrofungi. The forests are dominated by trees in the Pinaceae with about 20 species in the genera Abies, Larix, Picea, Pinus, Pseudotsuga, and Tsuga. All form ectomycorrhizas with fungi in the Basidiomycota, Ascomycota, and a few Zygomycota. Other ectomycorrhizal genera include Alnus, Arbutus, Arctostaphylos, Castinopsis, Corylus, Lithocarpus, Populus, Quercus, and Salix, often occurring as understorey or early-successional trees. Ectomycorrhizal fungi number in the thousands; as many as 2000 species associate with widespread dominant trees such as Douglas-fir (Pseudotsuga menziesii) (Trappe, 1977). The Pacific Northwest region also contains various ecozones on diverse soil types that range from extremely wet coastal forests to xeric interior forests, found at elevations from sea level to timber line at 2000 to 3000 metres. The combination of diverse ectomycorrhizal host trees inhabiting steep environmental and physical gradients has yielded perhaps the richest forest mycota of any temperate forest zone. When the large number of ectomycorrhizal species is added to the diverse array of saprotrophic and pathogenic fungi, the overall diversity of macrofungi becomes truly staggering. Issues relating to conservation and management of forest fungi in the

Hyphal mats formed by two ectomycorrhizal fungi and their association with Douglas-fir seedlings: A case study

The ectomycorrhizal fungi Gautieria monticola and Hysterangium setchellii both form dense hyphal mats in coniferous forest soils of the Pacific Northwest. We recently observed that all Douglas-fir seedlings found under the canopy of a maturing 60–75 year stand were associated with mats formed by ectomycorrhizal fungi. The significance of these mat communities in relation to seedling establishment and survival is discussed.

Consideration of the taxonomy and biodiversity of Australian ectomycorrhizal fungi

Mycorrhiza management in forestry must be predicated on an understanding of fungal biology and ecology. A fundamental building block of the biology and ecology of any organism is accurate identification and an understanding of its relationship to other organisms.The taxonomy of the larger fungi has been largely based on morphological classification of sexual structures but now Taxonomy routinely incorporates mating studies, and biochemical and molecular data. Taxonomy may not revolutionize theories on mycorrhiza but can clarify some of the inconsistencies due to misrepresentation or over-generalizations and inappropriate conclusions drawn from studies with inaccurately identified fungi. To illustrate this, we discuss and example where incorrect fungal names were repeatedly erroneously applied in morphological and physiological research reports on this fungus, e.g. Laccaria laccata. In this case subsequent taxonomic study revealed the reason for the conflicting research results reported for this fungus.We discuss the status of identifying the ectomycorrhizal fungi in various forest communities in Australia and the relationships of this process to assessing their use in forestry. Recent intensive efforts to collect, isolate and identify Australian ectomycorrhizal fungi have revealed an enormous and unique species diversity, e.g., for truffle-like fungi, over 2000 collections from the last five years alone have yielded 2 new families, 24 new genera, and about 184 new species. Nearly 95% of the described and undescribed fungi from Australia are novel, with some 22 genera and 3 families endemic. In most cases the current systematic knowledge of mycorrhizal fungi is inadequate to support clear framework for Australian taxa. This reflects the traditional Northern Hemisphere view of the world, the uniqueness of the Australian fungal flora, and how poorly it is known. For example, the genus Hymenogaster had been widely acknowledged as the most reduced member of the Cortinariaceae. However recent work on Hymenogaster species from the Southern Hemisphere has offered a number of alternative affinities to various species.We also discuss the role proper identification of the organisms involved plays in understanding the ecosystem. Emphasis should be placed on how species diversity equates with physiological and genetic diversity and how a sound taxonomic understanding of species and their systematic position is essential to properly manage them. Accurate taxonomic information will continue to be required as the basis for assessing the role of ectomycorrhizal fungi in sustained ecological development. Of particular significance is the role of ectomycorrhizal fungi in maintenance of plant diversity in natural ecosystems and those disturbed by management. In conclusion, we present some key research areas involving the use of taxonomy that need priority attention.

Microbial characteristics of ectomycorrhizal mat communities in Oregon and California

SummarySpecialized ectomycorrhizal fungi form dense mats in forest soils that have different enzyme levels, higher respiration rates, more biomass, different soil fauna, and different soil chemistry compared with adjacent soils not obviously colonized by these mats. In this study, mats formed by two genera of fungi collected in three locations were compared with a wide range of measurements. Per cent moisture, pH, chloroform fumigation-flush C, anaerobic N mineralization, exchangeable ammonium, and respiration, N2 fixation, and denitrification rates were compared between soils or litter colonized by ectomycorrhizal mat-forming fungi and adjacent non-mat material. Significant differences were observed between the two genera of mat-forming fungi and also between mats formed primarily in mineral soil and those formed in litter. These differences suggest that different mat-forming fungi perform different functions in forest soils and that these fungi function differently in mineral soil compared with litter.

Fatty acid esterase production by ectomycorrhizal fungi

Several reports have indicated the stimulating effeet of fatty acid-containing materials on the growth of ectomycorrhizal fungi. Growth of dif? ferent ectomycorrhizal fungi can be stimulated by lipids (Schisler and Volkoff, 1977; Fries et al, 1985), Tween 80 (Straatsma and Bruinsma, 1986), or certain free fatty acids (Lindeberg and Lin? deberg, 1974). Palmer and Hacskaylo (1970) re? ported no growth stimulation using the synthetic lipid triacetin, but this may have been the result of acetate inhibition (Lindeberg and Lindeberg, 1974) or the inability to use acetate as a sole carbon source.