The Leotiomycetes includes non-lichenized fungi producing a generally small apothecium with an exposed hymenium and an inoperculate, unitunicate ascus that has an apical perforation pore for releasing ascospores (Dennis 1968, Korf 1973, Nannfeldt 1932, Pfister and Kimbrough 2001). Recent molecular studies suggest that several groups of fungi with simple, cleistothecial ascomata belong to the Leotiomycetes, including the Erysiphales, Myxotrichaceae, and Thelebolales (Blackwell et al. 2006; de Hoog et al. 2005; Gernandt et al. 2001). Conversely, other groups traditionally included in the Leotiomycetes, such as the Geoglossaceae and Orbiliaceae, have been proved to be phylogenetically distinct (Spatafora et al. 2006; Wang et al. 2006). Currently, five orders, 21 families, and about 510 genera (115 with an uncertain position) are accepted in the Leotiomycetes on the basis of both traditional classification and molecular phylogenetic studies (Eriksson 2005, Kirk et al. 2001, Hibbett et al. 2007).

Morphologically and ecologically, the Leotiomycetes is a highly diverse group of the Pezizomycotina. For example, species of Cyttaria (Cyttariales) produce brightly colored globose fruiting bodies of "ping-pong ball" size on hard wood trees, while apothecia of Lophodermium (Rhytismatales) often mature as small, dark dots on conifer needles. The Erysiphales and Thelebolales are associated with distinct ecological characters and nutritional modes, in addition to morphology almost unique for each group. Members of the Helotiales thrive in various ecosystems and cover a broad range of niches, and helotialean fungi have been described as plant pathogens, endophytes, mycorrhizae, fungal parasites, terrestrial saprobes, aquatic saprobes, root symbionts, and wood rot fungi.

Many species of the Leotiomycetes are described from the temperate Northern Hemisphere, but some members within the Leotiomycetes are patchy in their broad geographic distribution. For example many fungi of the Sclerotiniaceae (Helotiales) are plant pathogens, and these fungi might have evolved primarily in the Northern Hemisphere. However, other genera, such as Cyttaria spp. and Chlorovibrissea, are only found in the Southern Hemisphere.

Asci of leotiomyceteous fungi and some other fungi (e.g. Sordariomycetes) are usually thin- and single-walled (unitunicate) with an apical perforation pore (inoperculate ascus) instead of a delicate lid-like apparatus (operculate ascus as that of Peziza species) for releasing ascospores. The traditional concept of the Leotiomycetes includes only fungi producing an apothecium which opens at a very early development stage with the hymenium exposed, so leotiomyceteous fungi are sometimes called inoperculate discomycetes (fungi with an apothecium) as well. The current concept of the Leotiomycetes includes fungal groups very different from each other in morphology. Some of them produce an ascocarp with the hymenium enclosed all the time or until the very late stage of their development, and this makes it difficult to integrate members of the class using just some key characters and to give a meaningful common name to the group. However, fungi of each order in the Leotiomycetes generally share a unique macromorphology, anatomic structure, and ecological role.

Cyttariales: There is a single family, Cyttariaceae, with a single genus, Cyttaria, of about a dozen parasitic species on southern beech (Nothofagus) in the Southern Hemisphere. The fungus produces large and fleshy globose or pyriform stromata with numerous separate, cup-shaped chambers containing asci and dark ascospores on galls of living branches. Different authors have used morphological evidence to place the genus variously in the Pezizales and the Helotiales (see discussion in Gamundí 1991). Megoni (1986) showed that the asci have a thin cell wall and an apical amyloid ring, characters shared by some helotialean fungi.

Erysiphales: The Erysiphales with one family of 15 genera (Braun et al. 2002, Takamatsu et al. 2005a, b) are obligate plant pathogens that cause powdery mildew (mitotic stages of these fungi can cover the host plant and give the infected area a unique, white-powder appearance) diseases on about 10,000 plant species (Amano 1986). There are no direct morphological features supporting inclusion of these fungi in the Leotiomycetes, and without exception, all Erysiphales have closed, non-ostiolate fruit-bodies with persistent asci and basal hymenium.

Rhytismatales: Many of the taxa placed in the Rhytismatales are poorly understood, and probably most fungi in this order have an endophytic life-style living harmlessly inside host plants. For most species the teleomorph comprises an apothecium with a very reduced excipulum, which develops within a dark stroma, and the stroma is typically immersed within host tissue and sometimes covered by a clypeus (Johnston 2001; Wang et al. 2002). The hymenium becomes exposed after the covering host and fungal tissue splits by one or more elongate slits. The asci are typically thin-walled, undifferentiated at the apex, nonamyloid, ascospores typically with gelatinous sheaths or appendages. The anamorphs are mostly Leptostroma-like, the spermatial conidia developing on often percurrently proliferating conidiogenous cells.

Thelebolales: Species of Thelebolus produce small, globose to disk-shaped ascomata with sometimes polysporus asci (ascus with more than 8 spores), and the development of the ascomata varies from a cleistohymenial type to a eugymnohymenial type (van Brummelen 1967). The Thelebolaceae has been placed in the Pezizales (Eckblad 1968, Kimbrough and Korf 1967), and this placement has been studied from the apothecium macro-morphology to ascus ultrastructure (Brummelen 1998). The placement of the Thelebolales in the Leotiomycetes is based on SSU-rDNA sequence data, and many of the order have still not been included in molecular phylogenetic studies (Gernandt et al. 2001, Landvik et al. 1998, Momol et al. 1996, de Hoog et al. 2005). Some species are coprophilous (on dung), and their sexual stage and prominent polysporus asci can be so easily induced in vitro that they have been used to demonstrate sexual development of ascomyceteous fungi.

Helotiales (with exclusion of the Geoglossaceae): As the largest order of the inoperculate discomycetes, helotialean fungi are characterized morphologically by an apothecium (cup- or disc-shaped) with an exposed hymenium and thin-walled, eight ascospores ascus with slightly thickened apices. Except for some famous plant pathogens, such as Sclerotinia sclerotiorum (also known as white mold) and Fabrella tsugae (also known as needle blight of Hemlock), life styles of most fungi in this order are unknown. Many members in the Helotiales were recorded as saprobic, but this requires much careful investigation. Especially if species have been recorded as host-restricted saprobes, often this relationship is an indication of an endophytic stage in their life cycle (Wang et al. 2006a, b).

Although fungi in the Leotiomycetes are morphologically diverse, as you can see from photographs of some representatives here, morphological characters used for taxonomy and classification of this class are very limited. We should admit that we have not done enough detailed studies about their morphology rather than saying these fungi are morphologically simple, and we just start to understand how ecological and biological factors play a role in shaping the evolutionary history and appearances of these interesting fungi.

Like most other ascomycetes, members of the Leotiomycetes have a predominantly asexual life cycle, via which large amounts of conidiospores (mitotic spores) are produced, and this character is critical for fungi, especially pathogens, to compete with other organisms for resources. But the life history of few leotiomyceteous fungi has been studied, and there are many leotiomyceteous fungi known only with either sexual (teleomorph) or asexual stages (anamorph). Anamorphs in various environmental samples, including some root endophytes and aquatic hyphomycetes, have been suggested to belong in the Leotiomycetes, but without any clear teleomorph connections. To make studies of this class even more difficult, there is little correlation between the classifications of teleomorphs and anamorphs in the Leotiomycetes (Marvanova 1997; Sutton and Hennebert 1994; also see Freshwater Ascomycetes and their Anamorphs).

View Leotiomycetes Tree

Current hypotheses about the relationships within Leotiomycetes are based on DNA sequences from the large, small and 5.8S subunits of the nuclear ribosome (de Hoog et al 2005; Gernandt et al 2001; Wang et al 2006).

The Leotiomycetes represents a morphologically and ecologically diverse class of Pezizomycotina whose evolutionary history is only beginning to be unraveled through phylogenetic analyses of molecular data. The traditional view of relationships within the Leotiomycetes has experienced significant changes. With very limited sampling, the Leotiomycetes (Eriksson 2005; Hibbett et al. 2007) excluding the Geoglossaceae and including the Pseudeurotiaceae is supported as a monophyletic group by rDNA data and protein coding gene data (Spatafora et al. 2006; Wang et al. 2006). Here we accept the Cyttariales, Erysiphales, Helotiales, Rhytismatales, Thelebolales, Myxotrichaceae and Pseudeurotiaceae as members of the Leotiomycetes based on analyses by the Assembling the Fungal Tree of Life (AFTOL) project and other previously published molecular phylogenies.

The placement of the Thelebolales in the Leotiomycetes is based on SSU-rDNA sequence data, and many representatives of this order have still not been included in molecular phylogenetic studies (e.g. Gernandt et al. 2001, Landvik et al. 1998, Momol et al. 1996). The Thelebolales may not be monophyletic, and its position in the Leotiomycetes should be regarded as a temporary treatment until sufficient proof becomes available. Myxotrichaceae and Pseudeurotiaceae are two families of cleistothecial ascomycetes, both of which contain genera linked to the Leotiomycetes in molecular studies (Sogonov et al. 2005, Sugiyama et al. 1999, Suh and Blackwell 1999). The molecular-based phylogenies are supported by electron microscope studies, with the highly reduced cleistothecial ascomata of Myxotrichum showing a striking similarity in morphogenesis and gross morphology to typical helotialean fungi such as Hymenoscyphus species (Tsuneda and Currah 2004). Inclusion of Pseudeurotiaceae in the Leotiomycetes is tentative, however, analysis of protein coding data of Pseudeurotium also supported its affinity to Leotia (Spatafora et al. 2006).

Within the Leotiomycetes, the Cyttariales, Rhytismatales and Erysiphales of current definition have been supported as monophyletic with both morphological and molecular characters. The current concept of the Helotiales (Eriksson 2005) almost certainly includes non-monophyletic taxa, and the Helotiales has received more attention recently (e.g. Gernandt et al. 2001, Lutzoni et al. 2004, Wang et al. 2005). Even with exclusion of groups such as the Cyttariales, Erysiphales, Myxotrichaceae, Pseudeurotiaceae, Geoglossaceae and genetically widely divergent taxa such as Chlorociboria and Neobulgaria species, the monophyly of the Helotiales is not supported by rDNA data, and relationships among major helotialean clades are uncertain. Relationships among major groups in the Leotiomycetes (equal to backbones of all published Leotiomycetes trees) were not resolved at all. However, several small and world-wide distributed genera, such as Ascocoryne, Bisporella, Bulgaria, Chlorociboria, Cordierites, Leotia and Microglossum, might be the key taxa for understanding the evolutionary history of the Leotiomycetes. Unfortunately molecular data for these fungi from different geographic regions are not available.

Significant advancements have been made in the phylogeny of the Leotiomycetes and include: the classification of Cudoniaceae in the Rhytismatales; the inclusion of the Erysiphales, Cyttariales, and Pseudeurotiaceae in the Leotiomycetes; and the exclusion of Geoglossaceae from the Leotiomycetes. Current taxon and character sampling is insufficient to address many of the internal nodes of the class, and future phylogenetic studies must strive to significantly increase character sampling, especially that of protein-coding genes, from the diversity of species characterized as inoperculate discomycetes

Collection Sites: world map showing specimen collection locations for Leotiomycetes

Barcode of Life Data Systems (BOLD) Stats
                                                             

Specimen Records:	148
Specimens with Sequences:	141
Specimens with Barcodes:	52
Public Records:	52
Species:	37
Species With Barcodes:	34

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