女婴服用“伟哥”遭吐槽 超说明书用药缺乏“国标”
.jpg)
A mycorrhiza (from Greek μ?κη? mykēs, "fungus", and ??ζα rhiza, "root"; pl.: mycorrhizae, mycorrhiza or mycorrhizas[1]) is a symbiotic association between a fungus and a plant.[2] The term mycorrhiza refers to the role of the fungus in the plant's rhizosphere, its root system. Mycorrhizae play important roles in plant nutrition, soil biology, and soil chemistry.
In a mycorrhizal association, the fungus colonizes the host plant's root tissues, either intracellularly as in arbuscular mycorrhizal fungi, or extracellularly as in ectomycorrhizal fungi.[3] The association is normally mutualistic. In particular species, or in particular circumstances, mycorrhizae may have a parasitic association with host plants.[4]
Definition
A mycorrhiza is a symbiotic association between a green plant and a fungus. The plant makes organic molecules by photosynthesis and supplies them to the fungus in the form of sugars or lipids, while the fungus supplies the plant with water and mineral nutrients, such as phosphorus, taken from the soil. Mycorrhizas are located in the roots of vascular plants, but mycorrhiza-like associations also occur in bryophytes[5] and there is fossil evidence that early land plants that lacked roots formed arbuscular mycorrhizal associations.[6] Most plant species form mycorrhizal associations, though some families like Brassicaceae and Chenopodiaceae cannot. Different forms for the association are detailed in the next section. The most common is the arbuscular type that is present in 70% of plant species, including many crop plants such as cereals and legumes.[7]
Evolution
Fossil and genetic evidence indicate that mycorrhizae are ancient, potentially as old as the terrestrialization of plants. Genetic evidence indicates that all land plants share a single common ancestor,[8] which appears to have quickly adopted mycorrhizal symbiosis, and research suggests that proto-mycorrhizal fungi were a key factor enabling plant terrestrialization.[9] The 400 million year old Rhynie chert contains an assemblage of fossil plants preserved in sufficient detail that arbuscular mycorrhizae have been observed in the stems of Aglaophyton major, giving a lower bound for how late mycorrhizal symbiosis may have developed.[6] Ectomycorrhizae developed substantially later, during the Jurassic period, while most other modern mycorrhizal families, including orchid and erchoid mycorrhizae, date to the period of angiosperm radiation in the Cretaceous period.[10] There is genetic evidence that the symbiosis between legumes and nitrogen-fixing bacteria is an extension of mycorrhizal symbiosis.[11] The modern distribution of mycorrhizal fungi appears to reflect an increasing complexity and competition in root morphology associated with the dominance of angiosperms in the Cenozoic Era, characterized by complex ecological dynamics between species.[12]
Types
Mycorrhizas are commonly divided into ectomycorrhizas and endomycorrhizas. The two types are differentiated by the fact that the hyphae of ectomycorrhizal fungi do not penetrate individual cells within the root, while the hyphae of endomycorrhizal fungi penetrate the cell wall and invaginate the cell membrane.[13][14] Endomycorrhiza includes arbuscular, ericoid, and orchid mycorrhiza, while arbutoid mycorrhizas can be classified as ectoendomycorrhizas. Monotropoid mycorrhizas form a special category.
Ectomycorrhiza
Ectomycorrhizas, or EcM, are symbiotic associations between the roots of around 10% of plant families, mostly woody plants including the birch, dipterocarp, eucalyptus, oak, pine, and rose[15] families, orchids,[16] and fungi belonging to the Basidiomycota, Ascomycota, and Zygomycota. Some EcM fungi, such as many Leccinum and Suillus, are symbiotic with only one particular genus of plant, while other fungi, such as the Amanita, are generalists that form mycorrhizas with many different plants.[17] An individual tree may have 15 or more different fungal EcM partners at one time.[18] Thousands of ectomycorrhizal fungal species exist, hosted in over 200 genera. A recent study has conservatively estimated global ectomycorrhizal fungal species richness at approximately 7750 species, although, on the basis of estimates of knowns and unknowns in macromycete diversity, a final estimate of ECM species richness would probably be between 20,000 and 25,000.[19]
Ectomycorrhizas consist of a hyphal sheath, or mantle, covering the root tip and a Hartig net of hyphae surrounding the plant cells within the root cortex. In some cases the hyphae may also penetrate the plant cells, in which case the mycorrhiza is called an ectendomycorrhiza. Outside the root, ectomycorrhizal extramatrical mycelium forms an extensive network within the soil and leaf litter.
Nutrients can be shown to move between different plants through the fungal network. Carbon has been shown to move from paper birch seedlings into adjacent Douglas-fir seedlings, although not conclusively through a common mycorrhizal network,[20] thereby promoting succession in ecosystems.[21] The ectomycorrhizal fungus Laccaria bicolor has been found to lure and kill springtails to obtain nitrogen, some of which may then be transferred to the mycorrhizal host plant. In a study by Klironomos and Hart, Eastern White Pine inoculated with L. bicolor was able to derive up to 25% of its nitrogen from springtails.[22][23] When compared with non-mycorrhizal fine roots, ectomycorrhizae may contain very high concentrations of trace elements, including toxic metals (cadmium, silver) or chlorine.[24]
The first genomic sequence for a representative of symbiotic fungi, the ectomycorrhizal basidiomycete L. bicolor, was published in 2008.[25] An expansion of several multigene families occurred in this fungus, suggesting that adaptation to symbiosis proceeded by gene duplication. Within lineage-specific genes those coding for symbiosis-regulated secreted proteins showed an up-regulated expression in ectomycorrhizal root tips suggesting a role in the partner communication. L. bicolor is lacking enzymes involved in the degradation of plant cell wall components (cellulose, hemicellulose, pectins and pectates), preventing the symbiont from degrading host cells during the root colonisation. By contrast, L. bicolor possesses expanded multigene families associated with hydrolysis of bacterial and microfauna polysaccharides and proteins. This genome analysis revealed the dual saprotrophic and biotrophic lifestyle of the mycorrhizal fungus that enables it to grow within both soil and living plant roots. Since then, the genomes of many other ectomycorrhizal fungal species have been sequenced further expanding the study of gene families and evolution in these organisms.[26]
Arbutoid mycorrhiza
This type of mycorrhiza involves plants of the Ericaceae subfamily Arbutoideae. It is however different from ericoid mycorrhiza and resembles ectomycorrhiza, both functionally and in terms of the fungi involved.[27] It differs from ectomycorrhiza in that some hyphae actually penetrate into the root cells, making this type of mycorrhiza an ectendomycorrhiza.[28]
Endomycorrhiza
Endomycorrhizas are variable and have been further classified as arbuscular, ericoid, arbutoid, monotropoid, and orchid mycorrhizas.[29]
Arbuscular mycorrhiza
Arbuscular mycorrhizas, (formerly known as vesicular-arbuscular mycorrhizas), have hyphae that penetrate plant cells, producing dichotomously branching invaginations (arbuscules) as a means of nutrient exchange. Often, balloon-like storage structures, termed vesicles, are also produced. In this interaction, fungal hyphae do not in fact penetrate the protoplast (i.e. the interior of the cell), but invaginate the cell membrane, creating a so-called peri-arbuscular membrane. The structure of the arbuscules greatly increases the contact surface area between the hypha and the host cell cytoplasm to facilitate the transfer of nutrients between them. Arbuscular mycorrhizas are fungi that are obligate biotrophs, meaning that they use the plant host for both growth and reproduction.[30] Twenty percent of the photosynthetic products made by the plant host are consumed by the fungi, the transfer of carbon from the terrestrial host plant is then exchanged by equal amounts of phosphate from the fungi to the plant host.[31]
Arbuscular mycorrhizas are formed only by fungi in the division Glomeromycota. Fossil evidence[6] and DNA sequence analysis[32] suggest that this mutualism appeared 400-460 million years ago, when the first plants were colonizing land. Arbuscular mycorrhizas are found in 85% of all plant families, and occur in many crop species.[15] The hyphae of arbuscular mycorrhizal fungi produce the glycoprotein glomalin, which may be one of the major stores of carbon in the soil.[33] Arbuscular mycorrhizal fungi have (possibly) been asexual for many millions of years and, unusually, individuals can contain many genetically different nuclei (a phenomenon called heterokaryosis).[34]
Ericoid mycorrhiza
Ericoid mycorrhizas are the third of the three more ecologically important types. They have a simple intraradical (growth in cells) phase, consisting of dense coils of hyphae in the outermost layer of root cells. There is no periradical phase and the extraradical phase consists of sparse hyphae that don't extend very far into the surrounding soil. They might form sporocarps (probably in the form of small cups), but their reproductive biology is poorly understood.[14]
Ericoid mycorrhizas have also been shown to have considerable saprotrophic capabilities, which would enable plants to receive nutrients from not-yet-decomposed materials via the decomposing actions of their ericoid partners.[36]
Orchid mycorrhiza
All orchids are myco-heterotrophic at some stage during their lifecycle, meaning that they can survive only if they form orchid mycorrhizas with basidiomycete fungi.[citation needed] Their hyphae penetrate into the root cells and form pelotons (coils) for nutrient exchange.[citation needed]
Monotropoid mycorrhiza
This type of mycorrhiza occurs in the subfamily Monotropoideae of the Ericaceae, as well as several genera in the Orchidaceae. These plants are heterotrophic or mixotrophic and derive their carbon from the fungus partner. This is thus a non-mutualistic, parasitic type of mycorrhizal symbiosis.[citation needed]
Mutualist dynamics
Mycorrhizal fungi form a mutualistic relationship with the roots of most plant species. In such a relationship, both the plants themselves and those parts of the roots that host the fungi, are said to be mycorrhizal. Relatively few of the mycorrhizal relationships between plant species and fungi have been examined to date, but 95% of the plant families investigated are predominantly mycorrhizal either in the sense that most of their species associate beneficially with mycorrhizae, or are absolutely dependent on mycorrhizae. The Orchidaceae are notorious as a family in which the absence of the correct mycorrhizae is fatal even to germinating seeds.[37]
Recent research into ectomycorrhizal plants in boreal forests has indicated that mycorrhizal fungi and plants have a relationship that may be more complex than simply mutualistic. This relationship was noted when mycorrhizal fungi were unexpectedly found to be hoarding nitrogen from plant roots in times of nitrogen scarcity. Researchers argue that some mycorrhizae distribute nutrients based upon the environment with surrounding plants and other mycorrhizae. They go on to explain how this updated model could explain why mycorrhizae do not alleviate plant nitrogen limitation, and why plants can switch abruptly from a mixed strategy with both mycorrhizal and nonmycorrhizal roots to a purely mycorrhizal strategy as soil nitrogen availability declines.[38] It has also been suggested that evolutionary and phylogenetic relationships can explain much more variation in the strength of mycorrhizal mutualisms than ecological factors.[39]
Sugar-water/mineral exchange
The mycorrhizal mutualistic association provides the fungus with relatively constant and direct access to carbohydrates, such as glucose and sucrose.[40] The carbohydrates are translocated from their source (usually leaves) to root tissue and on to the plant's fungal partners. In return, the plant gains the benefits of the mycelium's higher absorptive capacity for water and mineral nutrients, partly because of the large surface area of fungal hyphae, which are much longer and finer than plant root hairs, and partly because some such fungi can mobilize soil minerals unavailable to the plants' roots. The effect is thus to improve the plant's mineral absorption capabilities.[41]
Unaided plant roots may be unable to take up nutrients that are chemically or physically immobilised; examples include phosphate ions and micronutrients such as iron. One form of such immobilization occurs in soil with high clay content, or soils with a strongly basic pH. The mycelium of the mycorrhizal fungus can, however, access many such nutrient sources, and make them available to the plants they colonize.[42] Thus, many plants are able to obtain phosphate without using soil as a source. Another form of immobilisation is when nutrients are locked up in organic matter that is slow to decay, such as wood, and some mycorrhizal fungi act directly as decay organisms, mobilising the nutrients and passing some onto the host plants; for example, in some dystrophic forests, large amounts of phosphate and other nutrients are taken up by mycorrhizal hyphae acting directly on leaf litter, bypassing the need for soil uptake.[43] Inga alley cropping, an agroforestry technique proposed as an alternative to slash and burn rainforest destruction,[44] relies upon mycorrhiza within the root system of species of Inga to prevent the rain from washing phosphorus out of the soil.[45]
In some more complex relationships, mycorrhizal fungi do not just collect immobilised soil nutrients, but connect individual plants together by mycorrhizal networks that transport water, carbon, and other nutrients directly from plant to plant through underground hyphal networks.[46]
Suillus tomentosus, a basidiomycete fungus, produces specialized structures known as tuberculate ectomycorrhizae with its plant host lodgepole pine (Pinus contorta var. latifolia). These structures have been shown to host nitrogen fixing bacteria which contribute a significant amount of nitrogen and allow the pines to colonize nutrient-poor sites.[47]
Mechanisms
The mechanisms by which mycorrhizae increase absorption include some that are physical and some that are chemical. Physically, most mycorrhizal mycelia are much smaller in diameter than the smallest root or root hair, and thus can explore soil material that roots and root hairs cannot reach, and provide a larger surface area for absorption. Chemically, the cell membrane chemistry of fungi differs from that of plants. For example, they may secrete organic acids that dissolve or chelate many ions, or release them from minerals by ion exchange.[48] Mycorrhizae are especially beneficial for the plant partner in nutrient-poor soils.[49]
Disease, drought and salinity resistance and its correlation to mycorrhizae
Mycorrhizal plants are often more resistant to diseases, such as those caused by microbial soil-borne pathogens. These associations have been found to assist in plant defense both above and belowground. Mycorrhizas have been found to excrete enzymes that are toxic to soil borne organisms such as nematodes.[50] More recent studies have shown that mycorrhizal associations result in a priming effect of plants that essentially acts as a primary immune response. When this association is formed a defense response is activated similarly to the response that occurs when the plant is under attack. As a result of this inoculation, defense responses are stronger in plants with mycorrhizal associations.[51] Ecosystem services provided by mycorrhizal fungi may depend on the soil microbiome.[52] Furthermore, mycorrhizal fungi was significantly correlated with soil physical variable, but only with water level and not with aggregate stability[53][54] and can lead also to more resistant to the effects of drought.[55][56][57] Moreover, the significance of mycorrhizal fungi also includes alleviation of salt stress and its beneficial effects on plant growth and productivity. Although salinity can negatively affect mycorrhizal fungi, many reports show improved growth and performance of mycorrhizal plants under salt stress conditions.[58]
Resistance to insects
Plants connected by mycorrhizal fungi in mycorrhizal networks can use these underground connections to communicate warning signals.[59][60] For example, when a host plant is attacked by an aphid, the plant signals surrounding connected plants of its condition. Both the host plant and those connected to it release volatile organic compounds that repel aphids and attract parasitoid wasps, predators of aphids.[59] This assists the mycorrhizal fungi by conserving its food supply.[59]
Colonization of barren soil
Plants grown in sterile soils and growth media often perform poorly without the addition of spores or hyphae of mycorrhizal fungi to colonise the plant roots and aid in the uptake of soil mineral nutrients.[61] The absence of mycorrhizal fungi can also slow plant growth in early succession or on degraded landscapes.[62] The introduction of alien mycorrhizal plants to nutrient-deficient ecosystems puts indigenous non-mycorrhizal plants at a competitive disadvantage.[63] This aptitude to colonize barren soil is defined by the category Oligotroph.
Resistance to toxicity
Fungi have a protective role for plants rooted in soils with high metal concentrations, such as acidic and contaminated soils. Pine trees inoculated with Pisolithus tinctorius planted in several contaminated sites displayed high tolerance to the prevailing contaminant, survivorship and growth.[64] One study discovered the existence of Suillus luteus strains with varying tolerance of zinc. Another study discovered that zinc-tolerant strains of Suillus bovinus conferred resistance to plants of Pinus sylvestris. This was probably due to binding of the metal to the extramatricial mycelium of the fungus, without affecting the exchange of beneficial substances.[63]
Occurrence of mycorrhizal associations
Mycorrhizas are present in 92% of plant families studied (80% of species),[15] with arbuscular mycorrhizas being the ancestral and predominant form,[15] and the most prevalent symbiotic association found in the plant kingdom.[40] The structure of arbuscular mycorrhizas has been highly conserved since their first appearance in the fossil record,[6] with both the development of ectomycorrhizas, and the loss of mycorrhizas, evolving convergently on multiple occasions.[15]
Associations of fungi with the roots of plants have been known since at least the mid-19th century. However early observers simply recorded the fact without investigating the relationships between the two organisms.[65] This symbiosis was studied and described by Franciszek Kamieński in 1879–1882.[66][67]
Climate change
CO2 released by human activities is causing climate change and possible damage to mycorrhizae, but the direct effect of an increase in the gas should be to benefit plants and mycorrhizae.[68] In Arctic regions, nitrogen and water are harder for plants to obtain, making mycorrhizae crucial to plant growth.[69] Since mycorrhizae tend to do better in cooler temperatures, warming could be detrimental to them.[70] Gases such as SO2, NO-x, and O3 produced by human activity may harm mycorrhizae, causing reduction in "propagules, the colonization of roots, degradation in connections between trees, reduction in the mycorrhizal incidence in trees, and reduction in the enzyme activity of ectomycorrhizal roots."[71]
Conservation and mapping
In 2021 the Society for the Protection of Underground Networks was launched. SPUN is a science-based initiative to map and protect the mycorrhizal networks that regulate the Earth’s climate and ecosystems. The stated goals of SPUN are mapping, protecting, and harnessing mycorrhizal fungi.
See also
- Effect of climate change on plant biodiversity
- Endosymbiont
- Epibiont, an organism that grows on another life form
- Endophyte
- Epiphyte
- Epiphytic fungus
- Mucigel
- Mycorrhizal fungi and soil carbon storage
- Mycorrhizal network
- Rhizobia
- Suzanne Simard
References
- ^ Deacon, Jim. "The Microbial World: Mycorrhizas". bio.ed.ac.uk (archived). Archived from the original on 2025-08-08. Retrieved 11 January 2019.
- ^ Kirk, P. M.; Cannon, P. F.; David, J. C.; Stalpers, J. (2001). Ainsworth and Bisby's Dictionary of the Fungi (9th ed.). Wallingford, UK: CAB International.
- ^ Wu, Qiang-Sheng, ed. (2017). Arbuscular Mycorrhizas and Stress Tolerance of Plants (1st ed.). Springer Singapore. p. 1. doi:10.1007/978-981-10-4115-0. ISBN 978-981-10-4115-0.
- ^ Johnson, N. C.; Graham, J. H.; Smith, F. A. (1997). "Functioning of mycorrhizal associations along the mutualism–parasitism continuum". New Phytologist. 135 (4): 575–585. doi:10.1046/j.1469-8137.1997.00729.x. S2CID 42871574.
- ^ Kottke, I.; Nebel, M. (2005). "The evolution of mycorrhiza‐like associations in liverworts: An update". New Phytologist. 167 (2): 330–334. doi:10.1111/j.1469-8137.2005.01471.x. PMID 15998388.
- ^ a b c d Remy, W.; Taylor, T. N.; Hass, H.; Kerp, H. (6 December 1994). "Four hundred-million-year-old vesicular arbuscular mycorrhizae". Proceedings of the National Academy of Sciences. 91 (25): 11841–11843. Bibcode:1994PNAS...9111841R. doi:10.1073/pnas.91.25.11841. PMC 45331. PMID 11607500.
- ^ Fortin, J. André; et al. (2015). Les Mycorhizes (second ed.). Versaillles: Inra. p. 10. ISBN 978-2-7592-2433-3.
- ^ Harris, Brogan J.; Clark, James W.; Schrempf, Dominik; Sz?ll?si, Gergely J.; Donoghue, Philip C. J.; Hetherington, Alistair M.; Williams, Tom A. (2025-08-08). "Divergent evolutionary trajectories of bryophytes and tracheophytes from a complex common ancestor of land plants". Nature Ecology & Evolution. 6 (11): 1634–1643. doi:10.1038/s41559-022-01885-x. PMC 9630106. PMID 36175544.
- ^ Puginier, Camille; Keller, Jean; Delaux, Pierre-Marc (2025-08-08). "Plant–microbe interactions that have impacted plant terrestrializations". Plant Physiology. 190 (1): 72–84. doi:10.1093/plphys/kiac258. PMC 9434271. PMID 35642902.
- ^ Miyauchi, Shingo; Kiss, Enik?; Kuo, Alan; et al. (2020). "Large-scale genome sequencing of mycorrhizal fungi provides insights into the early evolution of symbiotic traits". Nature Communications. 11 (1): 5125. Bibcode:2020NatCo..11.5125M. doi:10.1038/s41467-020-18795-w. PMC 7550596. PMID 33046698.
- ^ Provorov, N. A.; Shtark, O. Yu; Dolgikh, E. A. (2016). "[Evolution of nitrogen-fixing symbioses based on the migration of bacteria from mycorrhizal fungi and soil into the plant tissues]". Zhurnal Obshchei Biologii. 77 (5): 329–345. PMID 30024143.
- ^ Brundrett, Mark C.; Tedersoo, Leho (2018). "Evolutionary history of mycorrhizal symbioses and global host plant diversity". New Phytologist. 220 (4): 1108–1115. doi:10.1111/nph.14976. PMID 29355963.
- ^ Harley, J. L.; Smith, S. E. 1983. Mycorrhizal symbiosis (1st ed.). Academic Press, London.
- ^ a b Allen, Michael F. 1991. The ecology of mycorrhizae. Cambridge University Press, Cambridge.
- ^ a b c d e Wang, B.; Qiu, Y.-L. (July 2006). "Phylogenetic distribution and evolution of mycorrhizas in land plants". Mycorrhiza. 16 (5): 299–363. doi:10.1007/s00572-005-0033-6. PMID 16845554. S2CID 30468942.
- ^ "Orchids and fungi: An unexpected case of symbiosis". American Journal of Botany. July 12, 2011. Archived from the original on 2025-08-08. Retrieved 24 July 2012.
- ^ den Bakker, Henk C.; Zuccarello, G. C.; Kuyper, Th. W.; Noordeloos, M. E. (July 2004). "Evolution and host specificity in the ectomycorrhizal genus Leccinum". New Phytologist. 163 (1): 201–215. doi:10.1111/j.1469-8137.2004.01090.x. PMID 33873790.
- ^ Saari, S. K.; Campbell, C. D.; Russell, J.; Alexander, I. J.; Anderson, I. C. (14 October 2004). "Pine microsatellite markers allow roots and ectomycorrhizas to be linked to individual trees". New Phytologist. 165 (1): 295–304. doi:10.1111/j.1469-8137.2004.01213.x. PMID 15720641.
- ^ Rinaldi, A. C.; Comandini, O.; Kuyper, T. W. (2008). "Ectomycorrhizal fungal diversity: separating the wheat from the chaff" (PDF). Fungal Diversity. 33: 1–45. Archived (PDF) from the original on 2025-08-08. Retrieved 2025-08-08.
- ^ Karst, Justine; Jones, Melanie D.; Hoeksema, Jason D. (2025-08-08). "Positive citation bias and overinterpreted results lead to misinformation on common mycorrhizal networks in forests". Nature Ecology & Evolution. 7 (4): 501–511. doi:10.1038/s41559-023-01986-1. ISSN 2397-334X. PMID 36782032. S2CID 256845005.
- ^ Simard, Suzanne W.; Perry, David A.; Jones, Melanie D.; Myrold, David D.; Durall, Daniel M. & Molina, Randy (1997). "Net transfer of carbon between ectomycorrhizal tree species in the field". Nature. 388 (6642): 579–582. Bibcode:1997Natur.388..579S. doi:10.1038/41557. S2CID 4423207.
- ^ Fungi kill insects and feed host plants BNET.com
- ^ Klironomos, J. N.; Hart, M. M. (2001). "Animal nitrogen swap for plant carbon". Nature. 410 (6829): 651–652. Bibcode:2001Natur.410..651K. doi:10.1038/35070643. PMID 11287942. S2CID 4418192.
- ^ Cejpková, J.; Gryndler, M.; Hr?elová, H.; Kotrba, P.; ?anda, Z.; Greňová, I.; Borovi?ka, J. (2016). "Bioaccumulation of heavy metals, metalloids, and chlorine in ectomycorrhizae from smelter-polluted area". Environmental Pollution. 218: 176–185. doi:10.1016/j.envpol.2016.08.009. PMID 27569718.
- ^ Martin, F.; Aerts, A.; et al. (2008). "The genome of Laccaria bicolor provides insights into mycorrhizal symbiosis" (PDF). Nature. 452 (7183): 88–92. Bibcode:2008Natur.452...88M. doi:10.1038/nature06556. PMID 18322534.
- ^ Miyauchi, Shingo; Kiss, Enik?; Kuo, Alan; Drula, Elodie; Kohler, Annegret; Sánchez-García, Marisol; Morin, Emmanuelle; Andreopoulos, Bill; Barry, Kerrie W.; Bonito, Gregory; Buée, Marc; Carver, Akiko; Chen, Cindy; Cichocki, Nicolas; Clum, Alicia (2025-08-08). "Large-scale genome sequencing of mycorrhizal fungi provides insights into the early evolution of symbiotic traits". Nature Communications. 11 (1): 5125. Bibcode:2020NatCo..11.5125M. doi:10.1038/s41467-020-18795-w. ISSN 2041-1723. PMC 7550596. PMID 33046698.
- ^ Brundrett, Mark (2004). "Diversity and classification of mycorrhizal associations". Biological Reviews. 79 (3). Wiley: 473–495. doi:10.1017/s1464793103006316. ISSN 1464-7931. PMID 15366760. S2CID 33371246.
- ^ "Some plants may depend more on friendly fungi than own leaves: Study". Business Standard. Press Trust of India. 20 October 2019.
- ^ Peterson, R. L.; Massicotte, H. B. & Melville, L. H. (2004). Mycorrhizas: anatomy and cell biology. National Research Council Research Press. ISBN 978-0-660-19087-7. Archived from the original on 2025-08-08.
- ^ Lanfranco, Luisa; Bonfante, Paola; Genre, Andrea (2025-08-08). Heitman, Joseph; Howlett, Barbara J. (eds.). "The Mutualistic Interaction between Plants and Arbuscular Mycorrhizal Fungi". Microbiology Spectrum. 4 (6): 4.6.14. doi:10.1128/microbiolspec.FUNK-0012-2016. hdl:2318/1627235. ISSN 2165-0497. PMID 28087942.
- ^ Kiers, E. Toby; Duhamel, Marie; Beesetty, Yugandhar; Mensah, Jerry A.; Franken, Oscar; Verbruggen, Erik; Fellbaum, Carl R.; Kowalchuk, George A.; Hart, Miranda M.; Bago, Alberto; Palmer, Todd M.; West, Stuart A.; Vandenkoornhuyse, Philippe; Jansa, Jan; Bücking, Heike (2025-08-08). "Reciprocal Rewards Stabilize Cooperation in the Mycorrhizal Symbiosis". Science. 333 (6044): 880–882. Bibcode:2011Sci...333..880K. doi:10.1126/science.1208473. ISSN 0036-8075. PMID 21836016. S2CID 44812991.
- ^ Simon, L.; Bousquet, J.; Lévesque, R. C.; Lalonde, M. (1993). "Origin and diversification of endomycorrhizal fungi and coincidence with vascular land plants". Nature. 363 (6424): 67–69. Bibcode:1993Natur.363...67S. doi:10.1038/363067a0. S2CID 4319766.
- ^ International Institute for Applied Systems Analysis (2025-08-08). "Plants and fungi together could slow climate change". phys.org -us. Retrieved 2025-08-08.
- ^ Hijri, M.; Sanders, I. R. (2005). "Low gene copy number shows that arbuscular mycorrhizal fungi inherit genetically different nuclei". Nature. 433 (7022): 160–163. Bibcode:2005Natur.433..160H. doi:10.1038/nature03069. PMID 15650740. S2CID 4416663.
- ^ Midgley, DJ; Chambers, SM; Cairney, J. W. G. (2002). "Spatial distribution of fungal endophyte genotypes in a Woollsia pungens (Ericaceae) root system". Australian Journal of Botany. 50 (5): 559–565. doi:10.1071/BT02020.
- ^ Read, D. J. & Perez-Moreno, J. (2003). "Mycorrhizas and nutrient cycling in ecosystems—a journey towards relevance?". New Phytologist. 157 (3): 475–492. doi:10.1046/j.1469-8137.2003.00704.x. PMID 33873410.
- ^ Trappe, J. M. (1987). "Phylogenetic and ecologic aspects of mycotrophy in the angiosperms from an evolutionary standpoint". In Safir, G. R. (ed.). Ecophysiology of VA Mycorrhizal Plants. Florida: CRC Press.
- ^ Franklin, O.; N?sholm, T.; H?gberg, P.; H?gberg, M. N. (2014). "Forests trapped in nitrogen limitation - an ecological market perspective on ectomycorrhizal symbiosis". New Phytologist. 203 (2): 657–666. doi:10.1111/nph.12840. PMC 4199275. PMID 24824576.
- ^ Hoeksema, Jason D.; Bever, James D.; Chakraborty, Sounak; Chaudhary, V. Bala; Gardes, Monique; Gehring, Catherine A.; Hart, Miranda M.; Housworth, Elizabeth Ann; Kaonongbua, Wittaya; Klironomos, John N.; Lajeunesse, Marc J.; Meadow, James; Milligan, Brook G.; Piculell, Bridget J.; Pringle, Anne; Rúa, Megan A.; Umbanhowar, James; Viechtbauer, Wolfgang; Wang, Yen-Wen; Wilson, Gail W. T.; Zee, Peter C. (16 August 2018). "Evolutionary history of plant hosts and fungal symbionts predicts the strength of mycorrhizal mutualism". Communications Biology. 1 (1): 116. doi:10.1038/s42003-018-0120-9. PMC 6123707. PMID 30271996.
- ^ a b Harrison, M. J. (2005). "Signaling in the arbuscular mycorrhizal symbiosis". Annu Rev Microbiol. 59: 19–42. doi:10.1146/annurev.micro.58.030603.123749. PMID 16153162.
- ^ Selosse, M. A.; Richard, F.; He, X.; Simard, S. W. (2006). "Mycorrhizal networks: des liaisons dangereuses?". Trends in Ecology and Evolution. 21 (11): 621–628. doi:10.1016/j.tree.2006.07.003. PMID 16843567.
- ^ Li, H.; Smith, S. E.; Holloway, R. E.; Zhu, Y.; Smith, F. A. (2006). "Arbuscular mycorrhizal fungi contribute to phosphorus uptake by wheat grown in a phosphorus-fixing soil even in the absence of positive growth responses". New Phytologist. 172 (3): 536–543. doi:10.1111/j.1469-8137.2006.01846.x. PMID 17083683.
- ^ Hogan, C.M. (2011). "Phosphate". In Jorgensen, A.; Cleveland, C.J. (eds.). Encyclopedia of Earth. Washington DC: National Council for Science and the Environment. Archived from the original on 2025-08-08.
- ^ Elkan, D. (21 April 2004). "Slash-and-burn farming has become a major threat to the world's rainforest". The Guardian.
- ^ "What is Inga alley cropping?". rainforestsaver.org. Archived from the original on 2025-08-08.
- ^ Simard, S.W.; Beiler, K.J.; Bingham, M.A.; Deslippe, J.R.; Philip, L.J.; Teste, F.P. (April 2012). "Mycorrhizal networks: mechanisms, ecology and modelling". Fungal Biology Reviews. 26 (1): 39–60. doi:10.1016/j.fbr.2012.01.001.
- ^ Paul, L. R.; Chapman, B. K.; Chanway, C. P. (1 June 2007). "Nitrogen Fixation Associated with Suillus tomentosus Tuberculate Ectomycorrhizae on Pinus contorta var. latifolia". Annals of Botany. 99 (6): 1101–1109. doi:10.1093/aob/mcm061. PMC 3243579. PMID 17468111.
- ^ Sylvia, David M.; Fuhrmann, Jeffry J.; Hartel, Peter G.; Zuberer, David A. (2005). "Overview of Mycorrhizal Symbioses". Principles and Applications of Soil Microbiology. Pearson Prentice Hall. ISBN 978-0-13-094117-6. Archived from the original on June 23, 2010.
- ^ "Botany online: Interactions - Plants - Fungi - Parasitic and Symbiotic Relations - Mycorrhiza". Biologie.uni-hamburg.de. Archived from the original on 2025-08-08. Retrieved 2025-08-08.
- ^ Azcón-Aguilar, C.; Barea, J. M. (29 October 1996). "Arbuscular mycorrhizas and biological control of soil-borne plant pathogens – an overview of the mechanisms involved". Mycorrhiza. 6 (6): 457–464. doi:10.1007/s005720050147. S2CID 25190159.
- ^ Jung, Sabine C.; Martinez-Medina, Ainhoa; Lopez-Raez, Juan A.; Pozo, Maria J. (24 May 2012). "Mycorrhiza-Induced Resistance and Priming of Plant Defenses". J Chem Ecol. 38 (6): 651–664. doi:10.1007/s10886-012-0134-6. PMID 22623151. S2CID 12918193.
- ^ Svenningsen, Nanna B; Watts-Williams, Stephanie J; Joner, Erik J; Battini, Fabio; Efthymiou, Aikaterini; Cruz-Paredes, Carla; Nybroe, Ole; Jakobsen, Iver (May 2018). "Suppression of the activity of arbuscular mycorrhizal fungi by the soil microbiota". The ISME Journal. 12 (5): 1296–1307. doi:10.1038/s41396-018-0059-3. PMC 5931975. PMID 29382946.
- ^ Zeng, Ren-Sen (2006). "Disease Resistance in Plants Through Mycorrhizal Fungi Induced Allelochemicals". Allelochemicals: Biological Control of Plant Pathogens and Diseases. Disease Management of Fruits and Vegetables. Vol. 2. pp. 181–192. doi:10.1007/1-4020-4447-X_10. ISBN 1-4020-4445-3.
- ^ "Dr. Susan Kaminskyj: Endorhizal Fungi". Usask.ca. Archived from the original on 2025-08-08. Retrieved 2025-08-08.
- ^ "Dr. Davies Research Page". Aggie-horticulture.tamu.edu. Archived from the original on 2025-08-08. Retrieved 2025-08-08.
- ^ Lehto, Tarja (1992). "Mycorrhizas and Drought Resistance of Picea sitchensis (Bong.) Carr. I. In Conditions of Nutrient Deficiency". New Phytologist. 122 (4): 661–668. doi:10.1111/j.1469-8137.1992.tb00094.x. JSTOR 2557434.
- ^ Nikolaou, N.; Angelopoulos, K.; Karagiannidis, N. (2003). "Effects of Drought Stress on Mycorrhizal and Non-Mycorrhizal Cabernet Sauvignon Grapevine, Grafted Onto Various Rootstocks". Experimental Agriculture. 39 (3): 241–252. doi:10.1017/S001447970300125X. S2CID 84997899.
- ^ Porcel, Rosa; Aroca, Ricardo; Ruiz-Lozano, Juan Manuel (January 2012). "Salinity stress alleviation using arbuscular mycorrhizal fungi. A review" (PDF). Agronomy for Sustainable Development. 32 (1): 181–200. doi:10.1007/s13593-011-0029-x. S2CID 8572482.
- ^ a b c Babikova, Zdenka; Gilbert, Lucy; Bruce, Toby J. A.; Birkett, Michael; Caulfield, John C.; Woodcock, Christine; Pickett, John A.; Johnson, David (July 2013). "Underground signals carried through common mycelial networks warn neighbouring plants of aphid attack". Ecology Letters. 16 (7): 835–843. doi:10.1111/ele.12115. PMID 23656527.
- ^ Johnson, David; Gilbert, Lucy (March 2015). "Interplant signalling through hyphal networks". New Phytologist. 205 (4): 1448–1453. doi:10.1111/nph.13115. PMID 25421970.
- ^ "Root fungi turn rock into soil". Planet Earth Online. 3 July 2009. Archived from the original on 2025-08-08.
- ^ Jeffries, Peter; Gianinazzi, Silvio; Perotto, Silvia; Turnau, Katarzyna; Barea, José-Miguel (January 2003). "The contribution of arbuscular mycorrhizal fungi in sustainable maintenance of plant health and soil fertility". Biology and Fertility of Soils. 37 (1): 1–16. doi:10.1007/s00374-002-0546-5. S2CID 20792333. INIST 14498927.
- ^ a b Richardson, David M. (2000). Ecology and biogeography of Pinus. London: Cambridge University Press. p. 336. ISBN 978-0-521-78910-3.
- ^ Tam, Paul C.F. (1995). "Heavy metal tolerance by ectomycorrhizal fungi and metal amelioration by Pisolithus tinctorius". Mycorrhiza. 5 (3): 181–187. doi:10.1007/BF00203335. hdl:10722/48503. S2CID 23867901.
- ^ Rayner, M. Cheveley (1915). "Obligate Symbiosis in Calluna vulgaris". Annals of Botany. 29 (113): 97–134. doi:10.1093/oxfordjournals.aob.a089540.
- ^ Kamieński, Franciszek (1882). "Les organes végétatifs de Monotropa hypopitys L."" [The vegetative organs of Monotropa hypopitys L.]. Mémoires de la Société nat. Des Sciences naturelles et mathém. De Cherbourg (in French). 3 (24).. Berch, S. M.; Massicotte, H. B.; Tackaberry, L. E. (July 2005). "Re-publication of a translation of 'The vegetative organs of Monotropa hypopitys L.' published by F. Kamienski in 1882, with an update on Monotropa mycorrhizas". Mycorrhiza. 15 (5): 323–32. doi:10.1007/s00572-004-0334-1. PMID 15549481. S2CID 3162281.
- ^ Kamieński, Franciszek (1885). "über die auf Wurzelsymbiose beruhende Ern?hrung gewisser B?ume durch unterirdische Pilze" [On the nourishing, via root symbiosis, of certain trees by underground fungi]. Berichte der Deutschen Botanischen Gesellschaft (in German). 3: 128–145. From p. 129: "Der ganze K?rper ist also weder Baumwurzel noch Pilz allein, sondern ?hnlich wie der Thallus der Flechten, eine Vereinigung zweier verschiedener Wesen zu einem einheitlichen morphologischen Organ, welches vielleicht passend als Pilzwurzel, Mycorhiza bezeichnet werden kann." (The whole body is thus neither tree root nor fungus alone, but similar to the thallus of lichens, a union of two different organisms into a single morphological organ, which can be aptly designated as a "fungus root", a mycorrhiza.)
- ^ Monz, C. A.; Hunt, H. W.; Reeves, F. B.; Elliott, E. T. (1994). "The response of mycorrhizal colonization to elevated CO2 and climate change in Pascopyrum smithii and Bouteloua gracilis". Plant and Soil. 165 (1): 75–80. doi:10.1007/bf00009964. S2CID 34893610.
- ^ Hobbie, John E.; Hobbie, Erik A.; Drossman, Howard; et al. (2009). "Mycorrhizal fungi supply nitrogen to host plants in Arctic tundra and boreal forests: 15N is the key signal". Canadian Journal of Microbiology. 55 (1): 84–94. doi:10.1139/w08-127. hdl:1912/2902. PMID 19190704.
- ^ Heinemeyer, A.; Fitter, A. H. (22 January 2004). "Impact of temperature on the arbuscular mycorrhizal (AM) symbiosis: growth responses of the host plant and its AM fungal partner". Journal of Experimental Botany. 55 (396): 525–534. doi:10.1093/jxb/erh049. PMID 14739273.
- ^ Xavier, L. J.; Germida, J. J. (1999). "Impact of human activities on mycorrhizae". Proceedings of the 8th International Symposium on Microbial Ecology.
External links
- International Mycorrhiza Society International Mycorrhiza Society
- Mohamed Hijri: A simple solution to the coming phosphorus crisis video recommending agricultural mycorrhiza use to conserve phosphorus reserves & 85% waste problem @Ted.com
- Mycorrhizal Associations: The Web Resource Comprehensive illustrations and lists of mycorrhizal and nonmycorrhizal plants and fungi
- Mycorrhizas – a successful symbiosis Biosafety research into genetically modified barley
- MycorWiki a portal concerned with the biology and ecology of ectomycorrhizal fungi and other forest fungi.
