The Agaricomycotina is one of three major clades of Basidiomycota (the others are the Pucciniomycotina and Ustilaginomycotina). The Agaricomycotina contains roughly 20,000 described species, which is almost 70% of the (known) Basidiomycota. About 98% of the species of the Agaricomycotina are in a clade called the Agaricomycetes, which includes mushrooms, bracket fungi, puffballs, and others. The other major groups are the Tremellomycetes and Dacrymycetes. These latter groups include "jelly fungi" (Fig. 1), which have gelatinous, often translucent fruiting bodies (e.g., "witches butter" Tremella mesenterica), as well as many yeast-forming species (Hibbett 2007).
Members of the Agaricomycotina display the full range of ecological strategies that characterizes the Basidiomycota as a whole. To obtain carbon nutrition, Agaricomycotina decompose dead organic matter or enter into diverse associations (both antagonistic and benign) with plants, animals, and other fungi. Mycorrhizal associations with plants are present in many lineages of Agaricomycetes, including certain jelly fungi (Selosse et al. 2002). Mycoparasitism (parasitism of a fungus by a fungus) is especially widespread in the Tremellomycetes (Bandoni 1984). Few Agaricomycotina are medically important. An exception is Filobasidiella neoformans (also called Cryptococcus neoformans), which is a serious pathogen of immunocompromised individuals (Mitchell and Perfect 1995).
Agaricomycotina include the vast majority of edible mushrooms, most of which are in the Agaricomycetes. Several jelly fungi are cultivated for food in Asia, including the "wood ear" fungus, Auricularia auricula-judae (Fig. 2), and the white jelly fungus, Tremella fuciformis.
Agaricomycotina are quite variable in both macroscopic and microscopic features. Traditionally, one of the most important characters in the higher-level taxonomy of Basidiomycota has been the form and septation of the basidia (the cells in which meiosis occurs, and on which sexual spores are formed) (Talbot, 1968; McNabb, 1973). Basidia of Agaricomycotina have various shapes and may be undivided or divided by transverse or longitudinal septa (Fig. 3). Previously--including in a former version of this Tree of Life page--the Agaricomycotina with "homobasidia" (which are undivided basidia that produce spores on short apical appendages, called sterigmata) were classified as the "Homobasidiomycetes". However, recent phylogenetic studies suggest that clades with undivided homobasidia are interdigitated with clades that have septate "heterobasidia". Consequently, the terms "homobasidiomycetes" and "heterobasidiomycetes" are no longer used to refer to formal taxa, but rather are used as descriptive terms only (Hibbett 2007).
Most Agaricomycotina produce four spores on each basidium, but some species produce as few as one or as many as eight spores per basidium. Another important character in prior taxonomy of Basidiomycota is the presence or absence of "spore repetition", which is the production of secondary spores directly from basidiospores. The Agaricomycotina display variation in this character also. It is therefore not surprising that the Agaricomycotina, as delimited here, was not formally recognized as a taxonomic group before the advent of molecular characters.
One unifying morphological feature of the Agaricomycotina is the presence of "dolipore" septa, which are pores in the crosswalls between adjacent cells that are bordered by a collar-like margin of cell wall material (Fig. 4). Other Basidiomycota also have septal pores, but their structure is not the same. Flanking the dolipores in almost all Agaricomycotina is a membrane-bound structure called a "septal pore cap". These structures are also called "parenthesomes", because they resemble parentheses around the septal pores when viewed in thin sections with transmission electron microscopy.
Variation in the form of the parenthesomes has provided clues to phylogenetic relationships in the Agaricomycotina (Adams et al. 1995; Bandoni and Oberwinkler 1982; Hibbett and Thorn 2001; McLaughlin et al. 1995; Moore, 1985; Swann and Taylor 1993; Wells and Bandoni 2001). Tremellomycetes have "vesiculate" parenthesomes, in which the septal pore cap is divided into cup-shaped sections. Dacrymycetes and some Agaricomycetes have "imperforate" parenthesomes, in which the septal pore cap forms a smooth, dome-shaped covering over the dolipore. Most Agaricomycetes have "perforate" parenthesomes, in which the septal pore cap has openings of varying sizes, and appears discontinuous in section.
Figure 4. Dolipore septa with perforate parenthesome (septal pore cap).
From Moore and Marchant (1972); used with permission.
Most known species of Agaricomycotina are filamentous and produce a multicellular fruiting body. The fruiting body is not always what most people would regard as a "mushroom", however. For example, in "resupinate" species the fruiting body is a flattened structure, which may be little more than a thin layer of hyphae produced on the underside of a log or some other inconspicuous location. As noted, some Agaricomycotina are yeasts and produce no fruiting body at all. Fruiting bodies of Agaricomycotina reach their greatest size, diversity, and complexity in the Agaricomycetes. It is likely that the yeasts and resupinate forms have been undercollected, relative to their more conspicuous relatives.
Fungus / feeder
Eleutheromyces coelomycetous anamorph of Eleutheromyces subulatus feeds on decaying carpophore of Basidiomycetes
Fungus / saprobe
fruitbody of Sistotrema brinkmannii is saprobic on dead, decayed fruitbody of Basidiomycetes
Other: unusual host/prey
Fungus / saprobe
fruitbody of Thanatephorus fusisporus is saprobic on dead, decayed fruitbody of Basidiomycetes
Evolution and Systematics
Discussion of Phylogenetic Relationships
As in all groups of Fungi, understanding of phylogenetic relationships in Agaricomycotina has advanced rapidly in recent years. Early phylogenetic analyses using rRNA gene sequences resolved many major groups within the Hymenomycetes, but higher-level relationships among these groups were often not resolved with confidence (Fell, 2001; Swann and Taylor, 1993; Swann et al. 1995). Recently, multi-locus analyses combining rRNA and protein-coding genes have improved resolution of the deepest splits in the Agaricomycotina (Matheny et al. 2006, 2007, Hibbett et al. 2007).
The phylogenetic hypothesis and classification adopted here are based on multiple independent analyses, summarized by Hibbett et al. (2007). Three major clades are formally named: Tremellomycetes, Dacrymycetes, and Agaricomycetes (which is here taken to include the heterobasidiomycetous Auriculariales and Sebacinales). Several analyses, including a multi-locus study by Matheny et al. (2007), suggest that the Dacrymycetes and Agaricomycetes form a monophyletic group, which Swann and Taylor (1995) called the Hymenomycetidae (here, the clade is unnamed). Earlier studies using rRNA genes did not support that grouping, however (Begerow et al. 1997; Weiß and Oberwinkler 2001).
To illustrate some of the changes that have taken place in phylogenetic reconstruction and classification in Agaricomycotina (and to help you make sense of older literature), the previous classifications of Agaricomycotina in the Tree of Life and the Dictionary of the Fungi 9th edition (Kirk et al. 2001) are presented below. In the former ToL classification, the Agaricomycotina was called the Hymenomycetes, following Swann and Taylor (1993), whereas in the Dictionary of the Fungi 9th ed. the group was called the Basidiomycetes (not to be confused with "basidiomycetes", which is a general term for all Basidiomycota). The Tremellomycetidae and Dacrymycetales of the previous ToL classification are equivalent to the Tremellomycetes and Dacrymycetes (respectively) of the current ToL classification. The current Agaricomycetes includes the Homobasidiomycetes and Auriculariales of the former ToL classification. The Tremellomycetidae of the Dictionary of the Fungi 9th edition is a paraphyletic group composed of "heterobasidiomycetes" (see Characteristics, above).
Table 1. Comparison of the previous classification of Agaricomycotina in the Tree of Life and that of Kirk et al. (2001).
|Previous ToL classification||Kirk et al. (2001)|
The most ancient divergences in the Agaricomycotina have been particularly difficult to resolve using only rRNA genes. For example, the tree below shows results of a study by Weiß and Oberwinkler (2001), who analyzed partial nuclear large subunit (nuc-lsu) rRNA gene sequences (names in the tree are based on the previous ToL classification). One source of error in earlier rRNA-based studies is an elevated rate of evolution of nuclear rRNA genes in some members of the Cantharellales, which is an early-diverging clade in the Agaricomycetes. Specifically, members of Cantharellus and Craterellus (which include edible chanterelles) and Tulasnella (a group of resupinate "crust fungi") have highly divergent nuc rRNA sequences that cannot be aligned in their entirety to other Agaricomycetes and produce conspicuously long branches in phylograms (Hibbett et al. 1997, Matheny et al. 2007, Moncalvo et al. 2007). Analyses using protein-coding genes leave little doubt that these taxa are in the Cantharellales clade of the Agaricomycetes (Matheny et al. 2007, Moncalvo et al. 2007).
Figure 5. Schematic representation of the phylogenetic tree of Weiß and Oberwinkler (2001). Numbers along branches indicate bootstrap frequencies. Bootstrap values below 60% are not shown. Taxon names are based on the previous classification in the Tree of Life.
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