Ectomycorrhizal extramatrical mycelium (also known as extraradical mycelium) is the collection of filamentous fungal hyphae emanating from ectomycorrhizas. It may be composed of fine, hydrophilic hypha which branches frequently to explore and exploit the soil matrix or may aggregate to form rhizomorphs; highly differentiated, hydrophobic, enduring, transport structures.
Apart from mycorrhizas, extramatrical mycelium is the primary vegetative body of ectomycorrhizal fungi. It is the location of mineral acquisition, enzyme production, and a key means of colonizing new root tips. Extramatrical mycelium facilitates the movement of carbon into the rhizosphere, moves carbon and nutrients between hosts and is an important food source for invertebrates.
The mycelial growth pattern, extent of biomass accumulation, and the presence or absence of rhizomorphs are used to classify fungi by exploration type. Agerer first proposed the designation of exploration types in 2001, and the concept has since been widely employed in studies of ectomycorrhizal ecology. Four exploration types are commonly recognized: Contact, Short-distance, Medium-distance and Long-distance.
Contact exploration types possess a predominantly smooth mantle and lack rhizomorphs with ectomycorrhizas in close contact with the surrounding substrate.
Short-distance exploration types also lack rhizomorphs but the mantle is surrounded by frequent projections of hyphae, which emanate a short distance into the surrounding substrate. Most ectomycorrhizal ascomycetes are included in this group.
Medium-distance exploration types are further divided into three subtypes defined by the growth range and differentiation of its rhizomorphs. Medium-distance Fringe form interconnected hyphal networks with rhizomorphs that divide and fuse repeatedly. Medium-distance Mat types form dense hyphal mats which aggregate into a homogeneous mass. Finally, the Medium-distance Smooth sub-type has rhizomorphs with smooth mantles and margins.
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An ectomycorrhiza (from Greek ἐκτός ektos, "outside", μύκης mykes, "fungus", and ῥίζα rhiza, "root"; pl. ectomycorrhizas or ectomycorrhizae, abbreviated EcM) is a form of symbiotic relationship that occurs between a fungal symbiont, or mycobiont, and the roots of various plant species. The mycobiont is often from the phyla Basidiomycota and Ascomycota, and more rarely from the Zygomycota. Ectomycorrhizas form on the roots of around 2% of plant species, usually woody plants, including species from the birch, dipterocarp, myrtle, beech, willow, pine and rose families.
A mycorrhizal network (also known as a common mycorrhizal network or CMN) is an underground network found in forests and other plant communities, created by the hyphae of mycorrhizal fungi joining with plant roots. This network connects individual plants together. Mycorrhizal relationships are most commonly mutualistic, with both partners benefiting, but can be commensal or parasitic, and a single partnership may change between any of the three types of symbiosis at different times.
Mycelial cords are linear aggregations of parallel-oriented hyphae. The mature cords are composed of wide, empty vessel hyphae surrounded by narrower sheathing hyphae. Cords may look similar to plant roots, and also frequently have similar functions; hence they are also called rhizomorphs (literally, "root-forms"). As well as growing underground or on the surface of trees and other plants, some fungi make mycelial cords which hang in the air from vegetation. Mycelial cords are capable of conducting nutrients over long distances.
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Abingdon2024
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