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Mycorrhizal Symbiosis (mycorrhizal + symbiosis)
Kinds of Mycorrhizal Symbiosis Selected AbstractsFoliar dehydration tolerance of mycorrhizal cowpea, soybean and bush beanNEW PHYTOLOGIST, Issue 2 2001Robert M. Augé Summary ,,Foliar dehydration tolerance of three mycorrhizal and nonmycorrhizal legumes is presented here. ,,Leaf water potential, osmotic adjustment and soil matric potential at the end of a lethal drying episode were compared in soybean, cowpea and bush bean colonized or uncolonized by Glomus intraradices. ,,Lethal leaf water potential were similar among treatments except in soybean, for which nonmycorrhizal plants given low phosphorus fertilization had values 0.3,0.4 MPa lower than mycorrhizal plants or nonmycorrhizal plants given higher phosphorus fertilization. Mycorrhizal symbiosis did not affect osmotic adjustment or lethal soil matric potential. Nonmycorrhizal cowpeas given low phosphorus showed more osmotic adjustment than nonmycorrhizal cowpeas given higher phosphorus. Foliage of host species typically classified as drought avoiders, cowpea and bush bean, survived to lower soil matric potentials than soybean, although soybean foliage was more tolerant of dehydration. ,,Our findings support the idea that when arbuscular mycorrhizal plants fare better than nonmycorrhizal plants during drought, it is probably due to enhanced drought avoidance capabilities conferred by the symbiosis rather than to changes in ability of foliage to withstand dehydration. [source] Phosphorus uptake, not carbon transfer, explains arbuscular mycorrhizal enhancement of Centaurea maculosa in the presence of native grassland speciesFUNCTIONAL ECOLOGY, Issue 6 2002C. A. Zabinski Summary 1Previous studies have shown that arbuscular mycorrhizas (AM) enhance the growth of the invasive forb Centaurea maculosa when growing with native grass species. Using 13CO2, we tested the hypothesis that this enhancement is explained by carbon transfer from native species to C. maculosa via mycorrhizal hyphal linkages. 2A C. maculosa plant was paired with one of five native species , three grasses (Festuca idahoensis, Koeleria cristata and Pseudoroegneria spicata) and two forbs (Achillea millefolium and Gaillardia aristata) , in pots that separated the plants with either a mesh barrier (28 µm, excludes fine roots but not hyphae) or a membrane barrier (0·45 µm, excludes roots and hyphae). 313CO2 was added to the atmosphere of either Centaurea or the native species after 20 weeks' growth. A 25 min pulse application was followed by 7 days' growth and subsequent harvest. 4The biomass response of C. maculosa was consistent with previous experiments: C. maculosa was larger when growing in mesh barrier pots, when hyphae were able to access the opposite side of the pot; in mesh barrier pots only, biomass varied with neighbouring species. Native plant biomass did not vary between mesh- vs membrane-barrier pots. 5There was no evidence of carbon transfer, either from the native plant to C. maculosa or in the reverse direction. 6Centaurea maculosa contained significantly more phosphorus in mesh-divided pots, but this depended on the neighbouring plant. The P concentration in C. maculosa was significantly higher in mesh-divided pots when growing with a grass and not a forb. Native species contained more P in mesh-divided pots than membrane-divided pots, and P concentration differed between species (higher in forbs than grasses), but did not vary between mesh- and membrane-divided pots. 7Our study suggests that C. maculosa is able to exploit its mycorrhizal symbiosis more effectively than the native grassland species. The mechanism for this appears to be luxury consumption of P through efficient utilization of extra-radical hyphae, but that effect is dependent on neighbouring species, and occurs when growing with a grass neighbour. 8Although no single study can disprove the carbon-transfer hypothesis, our work suggests that AM-mediated neighbour effects are the result of mycorrhizal networks that increase species' access to P. Whether the synergistic effects of neighbours are due to complementarity of AM fungal symbionts utilized by different plant species, or have to do with the structure of AM networks that develop more extensively with multiple host plants, remains to be investigated. [source] Plant and fungal identity determines pathogen protection of plant roots by arbuscular mycorrhizasJOURNAL OF ECOLOGY, Issue 6 2009Benjamin A. Sikes Summary 1.,A major benefit of the mycorrhizal symbiosis is that it can protect plants from below-ground enemies, such as pathogens. Previous studies have indicated that plant identity (particularly plants that differ in root system architecture) or fungal identity (fungi from different families within the Glomeromycota) can determine the degree of protection from infection by pathogens. Here, we test the combined effects of plant and fungal identity to assess if there is a strong interaction between these two factors. 2.,We paired one of two plants (Setaria glauca, a plant with a finely branched root system and Allium cepa, which has a simple root system) with one of six different fungal species from two families within the Glomeromycota. We assessed the degree to which plant identity, fungal identity and their interaction determined infection by Fusarium oxysporum, a common plant pathogen. 3.,Our results show that the interaction between plant and fungal identity can be an important determinant of root infection by the pathogen. Infection by Fusarium was less severe in Allium (simple root system) or when Setaria (complex root system) was associated with a fungus from the family Glomeraceae. We also detected significant plant growth responses to the treatments; the fine-rooted Setaria benefited more from associating with a member of the family Glomeraceae, while Allium benefited more from associating with a member of the family Gigasporaceae. 4.,Synthesis. This study supports previous claims that plants with complex root systems are more susceptible to infection by pathogens, and that the arbuscular mycorrhizal symbiosis can reduce infection in such plants , provided that the plant is colonized by a mycorrhizal fungus that can offer protection, such as the isolates of Glomus used here. [source] Giving and receiving: measuring the carbon cost of mycorrhizas in the green orchid, Goodyera repensNEW PHYTOLOGIST, Issue 1 2008Duncan D. Cameron Summary ,,Direct measurement of the carbon (C) ,cost' of mycorrhizas is problematic. Although estimates have been made for arbuscular and ectomycorrhizal symbioses, these are based on incomplete budgets or indirect measurements. Furthermore, the conventional model of unidirectional plant-to-fungus C flux is too simplistic. Net fungus-to-plant C transfer supports seedling establishment in c. 10% of plant species, including most orchids, and bidirectional C flows occur in ectomycorrhiza utilizing soil amino acids. ,,Here, the C cost of mycorrhizas to the green orchid Goodyera repens was determined by measurement of simultaneous bidirectional fluxes of 14C labelled sources using a monoxenic system with the fungus Ceratobasidium cornigerum. ,,Transfer of C from fungus to plant (,up-flow') occurs in the photosynthesizing orchid G. repens (max. 0.06 µg) whereas over five times more current assimilate (min. 0.355 µg) is simultaneously allocated in the reverse direction to the mycorrhizal fungus (,down-flow') after 8 d. Carbon is transferred rapidly, being detected in plant,fungal respiration within 31 h of labelling. ,,This study provides the most complete C budget for an orchid,mycorrhizal symbiosis, and clearly shows net plant-to-fungus C flux. The rapidity of bidirectional C flux is indicative of dynamic transfer at an interfacial apoplast as opposed to reliance on digestion of fungal pelotons. [source] Suillus bovinus glutamine synthetase gene organization, transcription and enzyme activities in the Scots pine mycorrhizosphere developed on forest humusNEW PHYTOLOGIST, Issue 2 2004Jarmo T. Juuti Summary ,,Glutamine synthetase (GS) expression and activity is of central importance for cellular ammonium assimilation and recycling. Thus, a full characterization of this enzyme at the molecular level is of critical importance for a better understanding of nitrogen (N) assimilation in the mycorrhizal symbiosis. ,,Genomic and cDNA libraries of Suillus bovinus were constructed to isolate the GS gene, glnA, and corresponding cDNAs. The transcription initiation site was identified and transcription and enzyme activities were characterized in pure culture mycelium and mycorrhiza, and extramatrical mycelium samples harvested from Scots pine,Suillus bovinus microcosms grown on forest humus. ,,Pure culture mycelium, mycorrhiza and extramatrical mycelium all exhibited equivalent levels of GS transcription, translation and enzyme activities. However, levels of transcription and enzyme activity did not correlate as a large majority of detectable transcripts showed specific 5,-end truncation. ,,Our data suggest that GS is constitutively expressed and not directly affected by environmental conditions of the symbiotic N uptake. Any changes in the intracellular ammonium level are most likely handled by regulatory flexibility of GS at enzyme level. [source] Functional complementarity in the arbuscular mycorrhizal symbiosisNEW PHYTOLOGIST, Issue 2 2000ROGER T. KOIDE The causes and consequences of biodiversity are central themes in ecology. Perhaps one reason for much of the current interest in biodiversity is the belief that the loss of species (by extinction) or their gain (by invasion) will significantly influence ecosystem function. Arbuscular mycorrhizal (AM) fungi are components of most terrestrial ecosystems and, while many research programs have shown that variability among species or isolates of AM fungi does occur (Giovannetti & Gianinazzi-Pearson, 1994), the basis for this variability and its consequences to the function of communities and ecosystems remains largely unexplored. Smith et al. (pp. 357,366 in this issue) now show clearly that ecologically significant functional diversity exists among AM fungal species in the regions of the soil from which they absorb phosphate, and their results suggest that such diversity may have significant ecological consequences. [source] Spatial differences in acquisition of soil phosphate between two arbuscular mycorrhizal fungi in symbiosis with Medicago truncatulaNEW PHYTOLOGIST, Issue 2 2000F. A. SMITH Responses of Medicago truncatula to colonization by two arbuscular mycorrhizal fungi, Scutellospora calospora isolate WUM 12(2) and Glomus caledonium isolate RIS 42, were compared in the light of previous findings that the former fungus can be ineffective as a beneficial microsymbiont with some host plants. The plants were grown individually in two-compartment systems in which a lateral side arm containing soil labelled with 33P was separated from the main soil compartment by a nylon mesh that prevented penetration by roots but not fungal hyphae. Fungal inoculum was applied as a root,soil mixture in a band opposite the side arm. Nonmycorrhizal controls were set up similarly, without inoculum. There were harvests at 28, 35, 42 and 49 d. Both sets of mycorrhizal plants grew better than nonmycorrhizal plants and initially had higher concentrations of P in shoots and roots. Plants grown with S. calospora grew better than plants grown with G. caledonium, and this was associated with somewhat greater fungal colonization in terms of intraradical hyphae and numbers of arbuscules. Scutellospora calospora formed denser hyphae at root surfaces than G. caledonium. By 28 d there were extensive hyphae of both fungi in the side arms, and after 35 d S. calospora produced denser hyphae there than G. caledonium. Nevertheless, there was very little transfer of 33P via S. calospora to the plant at 28 d, and thereafter its transfer increased at a rate only c. 33% of that via G. caledonium. The results showed that plants colonized by S. calospora preferentially obtained P from sites in the main soil chamber relatively close to the roots, compared with plants colonized by G. caledonium. Hence formation of a highly beneficial arbuscular mycorrhizal symbiosis does not necessarily depend on development of hyphae at a distance from the roots or on large-scale translocation of P from distant sites. The results are discussed in relation to previous studies with compartmented systems that have involved the same fungi. Possible causes of the variable effects of S. calospora in symbiosis with different host plants are briefly assessed. Differences in spatial abilities of individual arbuscular mycorrhizal fungi to acquire P might have strong ecological implications for plant growth in soils low in P. [source] Maize mutants affected at distinct stages of the arbuscular mycorrhizal symbiosisTHE PLANT JOURNAL, Issue 2 2006Uta Paszkowski Summary Maize mutants affected in the symbiotic interaction with the arbuscular mycorrhizal fungus Glomus mosseae have been found by a visual, macroscopic screen in a Mutator -tagged population of maize. Seven mutants have been identified, falling into three phenotypic classes. For each class one mutant has been characterized in more detail. The nope1 (noperception 1) mutant does not support appressoria formation of G. mosseae, suggesting the absence of a plant-encoded function necessary for early recognition prior to contact. The phenotype segregated as a monogenic recessive trait, indicating that a mutation in a single locus abolished compatibility of maize to G. mosseae. On a second mutant termed taci1 (taciturn 1), appressoria form at reduced frequency but their morphology is normal and leads to penetration of the rhizodermis. However, intraradically, the majority of hyphae are septate, resulting in terminated fungal spreading. This phenotype suggests that the mutation of taci1 has an effect on recognition and on cortex invasion. Segregation analysis indicates taci1 to carry a recessive mutation. In contrast, wild-type fungal morphology has been recorded in the Pram1 (Precocious arbuscular mycorrhiza 1) mutant, which displays enhanced and earlier fungal invasion. This trait segregates in a dominant fashion indicative of a gain-of-function mutation affecting the plant's control over restricting fungal colonization. [source] | ||||||||||