| Mortierellales | |
|---|---|
 | |
Scientific classification  | |
| Kingdom: | Fungi |
| Division: | Mucoromycota |
| Subdivision: | Mucoromycotina |
| Order: | Mortierellales |
MortierellalesCaval.-Sm., 1998 is a monotypic fungal order, [1] [2] within the phylum of Zygomycota and the monotypic, division of Mortierellomycota. [3] It contains only 1 known family, MortierellaceaeLuerss., Handb. Syst. Bot. 1: 63. 1877, and 6 genera and around 129 species.
The Urticaceae are a family, the nettle family, of flowering plants. The family name comes from the genus Urtica. The Urticaceae include a number of well-known and useful plants, including nettles in the genus Urtica, ramie, māmaki, and ajlai.
Hamamelidaceae, commonly referred to as the witch-hazel family, is a family of flowering plants in the order Saxifragales. The clade consists of shrubs and small trees positioned within the woody clade of the core Saxifragales. An earlier system, the Cronquist system, recognized Hamamelidaceae in the Hamamelidales order.
The opisthokonts are a broad group of eukaryotes, including both the animal and fungus kingdoms. The opisthokonts, previously called the "Fungi/Metazoa group", are generally recognized as a clade. Opisthokonts together with Apusomonadida and Breviata comprise the larger clade Obazoa.
The Boletaceae are a family of mushroom-forming fungi, primarily characterised by small pores on the spore-bearing hymenial surface, instead of gills as are found in most agarics. Nearly as widely distributed as the agarics, the family is renowned for hosting some prime edible species highly sought after by mushroom hunters worldwide, such as the cep or king bolete . A number of rare or threatened species are also present in the family, that have become the focus of increasing conservation concerns. As a whole, the typical members of the family are commonly known as boletes.
Internal transcribed spacer (ITS) is the spacer DNA situated between the small-subunit ribosomal RNA (rRNA) and large-subunit rRNA genes in the chromosome or the corresponding transcribed region in the polycistronic rRNA precursor transcript.
Microsporidia are a group of spore-forming unicellular parasites. These spores contain an extrusion apparatus that has a coiled polar tube ending in an anchoring disc at the apical part of the spore. They were once considered protozoans or protists, but are now known to be fungi, or a sister group to fungi. These fungal microbes are obligate eukaryotic parasites that use a unique mechanism to infect host cells. They have recently been discovered in a 2017 Cornell study to infect Coleoptera on a large scale. So far, about 1500 of the probably more than one million species are named. Microsporidia are restricted to animal hosts, and all major groups of animals host microsporidia. Most infect insects, but they are also responsible for common diseases of crustaceans and fish. The named species of microsporidia usually infect one host species or a group of closely related taxa. Approximately 10 percent of the species are parasites of vertebrates —several species, most of which are opportunistic, can infect humans, in whom they can cause microsporidiosis.
Glomeromycota are one of eight currently recognized divisions within the kingdom Fungi, with approximately 230 described species. Members of the Glomeromycota form arbuscular mycorrhizas (AMs) with the thalli of bryophytes and the roots of vascular land plants. Not all species have been shown to form AMs, and one, Geosiphon pyriformis, is known not to do so. Instead, it forms an endocytobiotic association with Nostoc cyanobacteria. The majority of evidence shows that the Glomeromycota are dependent on land plants for carbon and energy, but there is recent circumstantial evidence that some species may be able to lead an independent existence. The arbuscular mycorrhizal species are terrestrial and widely distributed in soils worldwide where they form symbioses with the roots of the majority of plant species (>80%). They can also be found in wetlands, including salt-marshes, and associated with epiphytic plants.
The Polyporaceae are a family of poroid fungi belonging to the Basidiomycota. The flesh of their fruit bodies varies from soft to very tough. Most members of this family have their hymenium in vertical pores on the underside of the caps, but some of them have gills or gill-like structures. Many species are brackets, but others have a definite stipe – for example, Polyporus badius.
The order Sordariales is one of the most diverse taxonomic groups within the Sordariomycetes.
The Pleosporales is the largest order in the fungal class Dothideomycetes. By a 2008 estimate it contains 23 families, 332 genera and more than 4700 species. The majority of species are saprobes on decaying plant material in fresh water, marine, or terrestrial environments, but several species are also associated with living plants as parasites, epiphytes or endophytes. The best studied species cause plant diseases on important agricultural crops e.g. Cochliobolus heterostrophus, causing southern corn leaf blight on maize, Phaeosphaeria nodorum causing glume blotch on wheat and Leptosphaeria maculans causing a stem canker on cabbage crops (Brassica). Some species of Pleosporales occur on animal dung and a small number occur as lichens and rock-inhabiting fungi.
The Arthoniales is the second largest order of mainly crustose lichens, but fruticose lichens are present as well. The order contains around 1500 species, while the largest order with lichenized fungi, the Lecanorales, contains more than 14000 species.
Atheliaceae is a family of corticioid fungi placed under the monotypic order Atheliales. Both the order and the family were described by Walter Jülich in 1981. According to a 2008 estimate, the family contains 20 genera and approximately 100 species. However, many genera formerly considered to belong in the Atheliaceae have since been moved to other families, including Amylocorticiaceae, Albatrellaceae, and Hygrophoraceae. Despite being a relatively small group with inconspicuous forms, Atheliaceae members show great diversity in life strategies and are widespread in distribution. Additionally, being a group strictly composed of corticioid fungi, they may also provide insights on the evolution of fruiting body forms in basidiomycetes.
The Baeomycetales are an order of mostly lichen-forming fungi in the subclass Ostropomycetidae, in the class Lecanoromycetes. It contains 8 families, 33 genera and about 170 species. As a result of molecular phylogenetics research published in the late 2010s, several orders were folded into the Baeomycetales, resulting in a substantial increase in the number of taxa.
Mucoromycotina is a subphylum of uncertain placement in Fungi. It was considered part of the phylum Zygomycota, but recent phylogenetic studies have shown that it was polyphyletic and thus split into several groups, it is now thought to be a paraphyletic grouping. Mucoromycotina is currently composed of 3 orders, 61 genera, and 325 species. Some common characteristics seen throughout the species include: development of coenocytic mycelium, saprotrophic lifestyles, and filamentous.
Dimargaritales is a monotypic order of fungi in the monotypic Dimargaritomycetes class within the subdivision of Kickxellomycotina.
The Mortierellaceae are a family of fungi in the order Mortierellales. The family contains six genera and 93 species.
Holozoa is a group of organisms that includes animals and their closest single-celled relatives, but excludes fungi. Holozoa is also an old name for the tunicate genus Distaplia.
Glomerellaceae is a monotypic family of fungi in the class Sordariomycetes that contains only one genus, Colletotrichum.
Trapeliaceae is a family of lichens in the order Baeomycetales. The family contains 12 genera and about 125 species.
Mucoromycota is a division within the kingdom fungi. It includes a diverse group of various molds, including the common bread molds Mucor and Rhizopus. It is a sister phylum to Dikarya.
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