A. Sponsors

B. Introduction

This site was developed as an online textbook to provide current information about mycorrhizal associations. Information about this site, instructions, acknowledgements and site history information is provided in Section 13.

All images on this site are protected by copyright and were taken by the author unless another photographer is named.

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Major Data Sources

C. Symbiosis and Mutualism

The terms symbiotic and mutualistic have been used interchangeably to describe mycorrhizal associations and parasitic fungi have also been called symbiotic, but many scientists now only call beneficial associations symbiotic (Lewis 1985, Paracer & Ahmadjian 2000). Symbiosis is defined broadly as “two or more organisms living together” and in most cases both partners benefit (Lewis 1985). There are many types of symbiosis evolving different combinations of plants, fungi, microbes and animals. Only plant-fungus associations are considered in detail here, but several others are illustrated below.

Fungal symbioses have been defined as “all associations where fungi come into contact with living host from which they obtain, in a variety of ways, either metabolites or nutrients” (Cook 1977). However, this definition excludes mycorrhizal associations of myco-heterotrophic plants, where plants are nutritionally dependant on fungi (Brundrett 2004). Only the broadest definition of symbiosis - “living together of two or more organisms”, applies universally to mycorrhizal associations (Lewis 1985, Smith & Read 1997, Brundrett 2004).

Mutualistic associations are a subset of symbioses where two or more different living organisms receive mutual benefits, as illustrated in the diagram below.

Diverse coral reef community on the Great Barrier Reef (Heron Island). Corals are symbiotic associations between an animal (coral polyp) and photosynthetic algae (zooxanthellae) inside the polyp.

Giant Clam (Tridacna gigas) in the Great Barrier Reef. Note algae in mantle (rollover image shows greater detail).

Nitrogen fixing symbiotic association of the cycad Macrozamia riedlei. These coralloid roots at the soil surface which contain cyanobacteria that fix nitrogen. Other nitrogen fixing associations include bacteria in nodules of peas (the Fabaceae) and actinomycete nodules in several other plant families.

The ash bolete (Gyrodon merulioides), which occurs under ash trees in North America (Fraxinus americana), has a symbiotic association with aphids (seen in cross section). See Section 10 for more information.

1. Plant-Fungal Symbioses

Mycorrhizas are the most important type of symbiotic plant-fungus associations, but there are a wide diversity of other associations between plants and fungi, as illustrated in the diagram below (pdf version). The relationship between mycorrhizas and other types of plant-fungus associations, such as parasitic or endophytic associations, are also shown below.

This diagram compares types of plant-fungus interactions and each is explained separately below (after Brundrett 2004).

Mutualistic associations occupy the mutual benefit (+ +) quadrant in diagrams contrasting the relative benefits (+) or harm (-) to two interacting organisms (Boucher 1985, Lewis 1985). This is a phase plane diagram that describes biological interactions according to a cost-benefit model, where mutualism is an isocline showing both partners are more successful together than they are alone (Boucher 1985, Lewis 1985, Tuomi et al. 2001).

Explanations

The vertical axis is a continuum of fungal harm or benefits.
The horizontal axis is a plant harm-benefit continuum.

Fungus benefits are linked to plant benefits in balanced mycorrhizas.
Obligate associations require greater investment from both partners than facultative mycorrhizas.

Exploitative mycorrhizas (myco-heterotrophs) are parallel to the vertical axis - plant benefit occurs at expense of fungi.

Parasitic plant-fungal associations are those where fungal benefits are linked to plant harm.

Endophytic plant-fungus associations (no plant harm or benefit).

Other categories of plant-fungus interactions include antagonism of fungi by plants or plants by fungi (causing harm to another organism without gaining direct benefits).

D. Definition of Mycorrhizas

The name mycorrhizas, which literally means fungus-root, was invented by Frank (1885) for non-pathogenic symbiotic associations between roots and fungi. A revised definition that includes non-mutualistic mycorrhizas and excludes other plant-fungus associations is provided below (Brundrett 2004). You should refer to review articles and books on mycorrhizas for further information about these associations.

Notes

  1. The structure and development of mycorrhizal fungus hyphae is substantially altered in the presence of roots of host plants. These root-borne hyphae are distinct from hyphae which are specialised for growth in soil.
  2. All mycorrhizas have intimate contact between hyphae and plant cells in an interface where nutrient exchange occurs.
  3. The primary role of mycorrhizas is the transfer of mineral nutrients from fungus to plant. In most cases there also is substantial transfer of metabolites from the plant to fungus.
  4. Mycorrhizas require synchronised plant-fungus development, since hyphae only colonise young roots (except orchid mycorrhizas and exploitative VAM).
  5. Plants control the intensity of mycorrhizas by root growth, digestion of old interface hyphae in plant cells (AM, orchid), or altered root system form (ECM).
  6. Roots evolved as habitats for mycorrhizal fungi (see Section 2). Mycorrhizas normally occur in roots, but can be hosted in stems in some cases (e.g. some orchids).

E. Categories of Mycorrhizal Associations

Consistent definitions of mycorrhizal associations are required for accurate communication of data. The flowchart below groups similar types of mycorrhizas together using categories regulated by the host and morphotypes caused by different fungi (pdf version). Categories and subcategories are defined in the subsequent table.

Hierarchical Classification Scheme for Mycorrhizal Associations (Brundrett 2004)

F. Morphology of Mycorrhizal Associations

The mycorrhizal association types defined in the table above are briefly described and illustrated below. More information on arbuscular mycorrhizas and ectomycorrhizas are provided in dedicated Sections of this site.

1. Arbuscular Mycorrhizas

Arbuscular mycorrhizas (Vesicular-Arbuscular Mycorrhizas, VAM or AM) are associations where Glomeromycete fungi produce arbuscules, hyphae, and vesicles within root cortex cells. These associations are defined by the presence of arbuscules. Fungi in roots spread by linear hyphae or coiled hyphae. VAM associations are described in detail in Section 4.

Arbuscule of a Glomus species in a root cortex cell. More information.

Vesicles of a Glomus species in a root cortex.
More information.

1.1. Linear association in root of Allium porrum with arbuscules (A) and vesicles (B) on longitudinal hyphae near entry point (arrow). More information.

1.2. Coiling association with arbuscules (A) on coiling hyphae (arrow) in a root of Erythronium americanum. More information.

1.2.1. Beaded roots (arrows) of Sugar Maple (Acer saccharum) - a VAM host. More information

1.2.2. Coiling association with arbuscules (A) only in the inner cortex layer of Asarum canadense roots.

1.2.3. Myco-heterotrophic "Arbuscular" Mycorrhizas

1.2.3. Coils of hyphae in the rhizome of Psilotum nudum a whisk fern. This is a type of VAM association without arbuscules from a young sporophyte with green shoots that is not fully myco-heterotrophic. See Section 2 for more information on mycorrhizas of primitive plants.

Cleared and stained rhizome
C = coil, V = vesicle
Roll-over animation shows a single coil.

2. Ectomycorrhizas

Ectomycorrhizas (ECM) are associations where fungi form a mantle around roots and a Hartig net between root cells. These associations are defined by Hartig net hyphae which grow around cells in the epidermis or cortex of short swollen lateral roots. ECM associations are described in Section 4. The former category of ECM is a morphotype (defined by fungi not hosts). Characteristics of this ECM morphotype are summarised by Yu et al. (2001).

2.1. Cortical Hartig net of Pinus ECM root.

Highly magnified view of cleared and stained section
More information

2.2. Epidermal Hartig net of Populus ECM.

Highly magnified view of cleared and stained section
More information.

Betula root system showing thicker branched or unbranched ECM roots borne on thinner lateral roots. ECM root systems are described in Section 5.


Magnified view of ECM root system
(grid = 1 mm).

2.2.2 Monotropoid

Monotropoid mycorrhizas are ECM associations of a few genera of myco-heterotrophic plants in the Ericaceae. These associations are characterised by limited hyphal penetration into epidermal cells. Information on structure of associations and the identity of mycorrhizal fungi in Monotropa, Pterospora, Sarcodes, etc. is provided by Robertson & Robertson (1982), Castellano & Trappe (1985) and Bidartondo et al. (2000).

2.2.2. Monotropa root with epidermal Hartig net (H) and mantle (M) in a cross-section viewed with UV light. Roll-over - hypha projecting into an epidermal cell (arrow) in stained root section.

Monotropa uniflora (Canada) is a myco-heterotrophic plant lacking chlorophyll that is entirely dependant on ECM fungi linked to nearby trees.

2.2.3 Arbutoid Mycorrhizas

Arbutoid mycorrhizal associations are variants of ECM found in certain plants in the Ericaceae characterised by hyphal coils in epidermal cells. These mycorrhizal roots are described by Largent et al. (1980), Molina & Trappe (1982) and Massicotte et al. (1998, 2005a). Gaultheria and Kalmia have ericoid mycorrhizas as well as arbutoid associations (Massicotte et al. 2005b).

2.2.3. Arbutus unedo root with Hartig net (arrows), coils (C) and mantle (M) of stained or unstained hyphae.

Highly magnified views of sectioned and cleared roots
(Bar = 20 µm)

3. Orchid Mycorrhizas

Orchid mycorrhizas consist of coils of hyphae within roots or stems of orchidaceous plants. Details of Orchid mycorrhizal associations are not provided here, but Australian Orchids found to have mycorrhizas are listed.

3.2. Orchid mycorrhizas with hyphae in trichomes and hyphal coils in stem of Pterostylis vittata

Highly magnified views of cleared and stained hand section.

3.1. Hyphal coils from orchid mycorrhizas in Epipactis helleborine root.

Highly magnified views of cleared and stained hand section.
More information

3.3. Hyphal coils (pelotons) of an exploitative mycorrhizal association in a myco-heterotrophic orchid. Coils are white of brown fuzzy balls. This rhizome of the Western Underground Orchid (Rhizanthella gardneri) is 5 mm wide.

Seedlings of Rhizanthella gardneri germinated by a mycorrhizal fungus linked to ECM roots of a shrub (Melaleuca sp.). These subterranean seedlings are 2-10 mm long with a zone of brown hyphal coils clearly visible at their base.

4. Ericoid Mycorrhizas

Ericoid mycorrhizas have hyphal coils in outer cells of the narrow "hair roots" of plants in the family Ericaceae. These associations are not described in detail here, but Australian plants with these mycorrhizas are listed.

Ericoid mycorrhizas with hyphal coils in hair roots of Leucopogon verticillatus

Highly magnified views of cleared and stained roots.
More Information

5. Subepidermal Association of Thysanotus

The Australian lilies in the genus Thysanotus (Laxmaniaceae) have unique mycorrhizas where fungus hyphae grow in a cavity under epidermal cells. Other members of this family have VAM or have NM roots (Section 8).

Highly magnified views of a sectioned and stained root of Thysanotus sp.
Arrows point to hyphae under the epidermis (E)

G. Host Plants

Comprehensive lists of Australian mycorrhizal plants, as well as plant families which are ECM hosts, or have NM roots are presented in Sections 5, 6 and 8 of this site. A summary of mycorrhizal associations in flowering and primitive plants are also provided in Section 2.

Field surveys have found that plants with mycorrhizal associations predominate in most natural ecosystems, as summarised the in table below.

  • Plants with VAM are common in most habitats
  • It is easier to say where they are not found
  • Trees with ECM are dominant in coniferous forests, especially in cold boreal or alpine regions
  • ECM trees and shrubs common in many broad-leaved forests in temperate or mediterranean regions
  • ECM trees also occur in some tropical or subtropical savanna or rain forests habitats
  • NM plants are most common in disturbed habitats, or sites with extreme environmental or soil conditions
  • NM plants appear to be more common in Australia than in other continents.

Data are from Brundrett (1991)

H. Mycorrhizal Fungi

Members of the fungus kingdom obtain nutrition from many sources, including decomposition of organic substrates, predation and parasitism, and involvement in mutualistic associations (Christensen 1989, Kendrick 1992). Mycorrhizal fungi are a major component of the soil microflora in many ecosystems, but usually have limited saprophytic abilities (Tanesaka et al. 1993, Hobbie et al. 2001). They are considered to have many important roles in natural and managed ecosystems as explained in Section 7. These fungi are introduced in the table below.

I. Terminology

Version 2 © Mark Brundrett 2008