Local reduction of mycorrhizal arbuscule frequency in enriched soil microsites

1994 ◽  
Vol 72 (7) ◽  
pp. 998-1001 ◽  
Author(s):  
S. E. Duke ◽  
R. B. Jackson ◽  
M. M. Caldwell

Increased nutrient availability reduces vesicular–arbuscular mycorrhizal (VAM) associations with plants, but whether increased nutrients in small volumes of soil affect local VAM colonization is not known. In a field experiment we investigated VAM colonization at different times following fertilization of small soil patches. Soil volumes of ~ 1000 cm3 were treated with a nutrient solution (enriched patch) or distilled water (control patch) on opposite sides of individual plants of the tussock grass Agropyron desertorum and the shrub Artemisia tridentata. Agropyron had significantly lower (p = 0.03) arbuscular infection in the locally enriched patches compared to control patches (32 and 40%, respectively). This reduced arbuscule frequency was apparent at the first sampling (3 days following treatment application) and remained lower in each subsequent sampling (as much as 30% lower than the control patches). Artemisia revealed a similar pattern in arbuscule frequency but was not statistically significant. Our results suggest that a plant can locally reduce VAM development, since arbuscule frequency specifically was locally reduced even though vesicle and overall infection was not. Since mycorrhizal infection does not increase, we conclude that increased plant root proliferation and uptake capacity are likely to be more important for the exploitation of temporary nutrient pulses or patches than is increased mycorrhizal activity. Key words: arbuscule, nutrient exploitation, phosphorus, reduced development, regulation of colonization, soil heterogeneity, vesicular–arbuscular mycorrhizae.

1993 ◽  
Vol 39 (6) ◽  
pp. 567-575 ◽  
Author(s):  
Narayan C. Talukdar ◽  
James J. Germida

Soil and root samples collected from fields cropped to spring wheat (Triticum aestivum L. cv. Katepwa) and lentil (Lens esculenta L. cv. Eston) at 11 sites across four soil zones of Saskatchewan were analyzed for spore numbers, level of vesicular–arbuscular mycorrhizal (VAM) colonization, and VAM species. The number of VAM spores detected in field soils ranged from 78 to 272 per 100 g soil. Vesicular–arbuscular mycorrhizae colonized wheat and lentil at all the field study sites, but levels of colonization in the two crops varied from site to site and the differences were more pronounced in wheat than in lentil. Generally, lentil both exhibited a higher percentage of VAM colonized roots and contained more arbuscules and vesicles than wheat roots. However, wheat appeared to be colonized by different types of VAM depending on the field sites. Differences in VAM colonization were not related to the moisture and temperature gradient of the four soil zones or soil properties. Seven VAM species were isolated by enriching indigenous VAM mixtures (collected from wheat field soils of six field sites) on maize. The VAM isolated most closely resembled Acaulospora denticulata, Gigaspora decipiens, Glomus clarum, Glomus etunicatum, Glomus fasciculatum, Glomus mosseae, and Glomus versiforme. The species composition of the VAM community varied at the different field sites.Key words: VAM, Acaulospora, Gigaspora, Glomus.


HortScience ◽  
1990 ◽  
Vol 25 (2) ◽  
pp. 183-189 ◽  
Author(s):  
F. Ponton ◽  
Y. Piché ◽  
S. Parent ◽  
M. Caron

The horticultural Boston fern [Nephrolepis exaltata (L.) Schott cv. Verona] was micropropagated in vitro using commercial techniques. Rooted plantlets were transferred into pots containing one of three test substrates made of peat and vermiculite and subsequently inoculated with one of two species of Glomus. Survival of uninoculated control plants growing on a black peat-based mix was less than that on a brown peat-based mix. Vesicular-arbuscular mycorrhizal (VAM) inoculation significantly increased survival on the former, but not the latter, substrate. The growth of roots was enhanced in brown peatmoss, but VAM colonization was faster with black peatmoss. Compared to uninoculated controls growing under the same fertilization regime, inoculated plants had significantly higher frond P and N concentration and also showed better frond and root growth. On a growth-increment basis, our results suggested that the brown peat-based mixed was more suitable for fungal activity and fern growth.


1993 ◽  
Vol 71 (9) ◽  
pp. 1169-1175 ◽  
Author(s):  
Victoria A. Borowicz

Vesicular–arbuscular mycorrhizae, defoliation, and competition can influence survival, growth, and fecundity of plants, but the combined effects of these factors are not well known. I examined how combinations of these factors influence biomass allocation and investment in root nodules by prereproductive Lotus corniculatus and whether the effects were ephemeral. Soil with vesicular–arbuscular mycorrhizal (VAM) fungi was treated with the fungicide benomyl or water and added to trays containing two L. corniculatus or one L. corniculatus and one Brassica napus (a nonmycotrophic species). Leaves of target L. corniculatus were undamaged or clipped five times over 40 days. Plants were harvested 5, 18, or 36 days after last clipping. Interspecific competition was the dominant effect at all harvests: B. napus greatly depressed growth of its neighbor. Benomyl depressed VAM colonization only in the first harvest, and growth reduction associated with depressed colonization diminished over time. Clipping reduced growth most in plants paired with conspecifics, but growth depression was transient. Benomyl and clipping reduced mass of root nodules in the first harvest. Benomyl reduced root mass in nontarget (competitor) L. corniculatus, but plants recovered with time. Neither benomyl nor clipping of the target plant affected B. napus. Interactions were few, indicating that the effects of factors were mostly additive. Key words: VAM fungi, resource allocation, nonmycotrophic competitor.


1992 ◽  
Vol 70 (1) ◽  
pp. 73-79 ◽  
Author(s):  
Gisela Cuenca ◽  
Milagros Lovera

Savannas growing on stony, old and nutrient-poor soils of southern Venezuela were severely disturbed by removal of the soil organic layers with bulldozers for road building. Introduced species Brachiaria decumbens, Brachiaria humidicola, Pueraria phaseoloides, and Calopogonium sp. were sown. The substrate was fertilized and limed. Plant cover, vesicular – arbuscular mycorrhizae colonization, spore number, and most probable number of propagulels in undisturbed savanna, disturbed nonrevegetated savanna, and six revegetated savannas were assessed. The perturbation reduced the mycorrhizal propagule number in comparison with the undisturbed savanna. In the nonrevegetated areas the mean percent ground cover 2 years after disturbance was low (0.04%). In revegetated areas an increase in mycorrhizal propagule number occurred and the mycorrhizal colonization of the sown species was high. In restored areas there was an increase in species of nonmycotrophic Amaranthaceae. The results support other predictions on the mycorrhizae in successional biomes, because in the extremely nutrient-poor soils studied the colonizing species were mainly mycotrophic. The reclamation program applied in disturbed areas was useful because it has allowed the recovery of vesicular – arbuscular mycorrhizal inoculum and there was an increase in the recolonization of native plants. Key words: disturbance, endomycorrhizae, revegetation, savanna, vesicular – arbuscular mycorrhizae.


1985 ◽  
Vol 15 (6) ◽  
pp. 1061-1064 ◽  
Author(s):  
Paul P. Kormanik

Sweetgum seedlings with vesicular–arbuscular mycorrhizae formed by Glomusetunicatum or Glomusdeserticola in nursery soil with 30 ppm available phosphorus (P) and nonmycorrhizal seedlings grown in nursery soil with 800 ppm available P were outplanted and whole trees were excavated periodically over the next 5 years in the plantation to follow mycorrhizal development. Four months after outplanting, roots of all initially nonmycorrhizal seedlings had formed vesicular–arbuscular mycorrhizae and the degree of root colonization was comparable to that of initially vesicular–arbuscular mycorrhizal seedlings. New feeder roots did not develop on seedlings of any treatment until almost 5 months after planting. By the end of the first growing season and for the remainder of the study, vesicular–arbuscular mycorrhizae development was approximately the same on all seedlings. The proportion of feeder roots colonized by vesicular–arbuscular mycorrhizal fungi stabilized at 65 to 70%; approximately 56% of the cortical tissues of all feeder roots were colonized with arbuscles, vesicles, and hyphae. Periodic assays of the soil in the plantation showed that vesicular–arbuscular mycorrhizal fungal spores gradually declined from an initial high of 3600 spores to 620 spores per 100-cm3 soil sample after 5 years. This decline was probably caused by crown closure of the sweetgum trees which gradually suppressed understory vegetation.


1996 ◽  
Vol 74 (5) ◽  
pp. 679-685 ◽  
Author(s):  
Paul Widden

During a survey of the vesicular–arbuscular mycorrhizal (VAM) associations of forest herbs in a deciduous forest in the southern Laurentian mountains in Quebec, two liliaceous species, Clintonia borealis and Medeola virginiana, revealed very distinctive morphology. In both species, once the epidermis was penetrated, the fungus spread towards the centre of the root via intracellular hyphae until the innermost layer of the cortex was reached, at which point the fungus spread laterally and tangentially through the cortical cells adjacent to the endodermis via a series of banana-shaped projections (bobbits). These eventually differentiated into the arbuscules and the VAM might spread from this inner cortical layer back into the outer cortical layers. In C. borealis, the hyphae coiled in the cortex, and vesicles were formed in the upper cortical cells. In M. virginiana, no coiling took place, but extensive diverticulae were produced by the intracellular hyphae in the cortical cells, close to their point of exit, and vesicles were produced in the inner cortex as swellings from the bobbits. These two mycorrhizae have some similarities to one in Colchicum autumnale described by I. Gallaud (1905. Rev. Gen. Bot. 17). Keywords: vesicular–arbuscular mycorrhizae, Clintonia borealis, Medeola virginiana, Liliaceae, morphology.


1977 ◽  
Vol 55 (1) ◽  
pp. 48-51 ◽  
Author(s):  
D. E. Carling ◽  
J. A. White ◽  
M. F. Brown

The ultrastructure of the interfacial zone which separates the intracellular structures of vesicular-arbuscular mycorrhizal fungi from host cytoplasm has been described in a variety of ways by recent investigators. Evidence is presented here which suggests that previous interpretations of the ultrastructure of the interfacial zone have been based on an artifact of fixation. Using an improved procedure, a dense, granular material was found in the interfacial zone. This material was preserved by simultaneous glutaraldehyde-osmium fixation but not by conventional prefixation and postfixation in glutaraldehyde and osmium, respectively.


HortScience ◽  
1994 ◽  
Vol 29 (11) ◽  
pp. 1362-1365 ◽  
Author(s):  
U. Afek ◽  
L.A. Lippet ◽  
D. Adams ◽  
J.A. Menge ◽  
E. Pond

Vesicular–arbuscular mycorrhizal inoculum consisting of a mixture of roots of coast redwood [Sequoia sempervirens (D. Don)], soil, and spores of Glomus mosseae (Nicol. and Gerd.) Gerdemann and Trappe was tested for viability and efficacy following storage for 4 or 8 weeks at 4, 9, 15, or 24C and moisture contents of 0%, 6%, 12%, or 17%. Storage regimes did not have any effect on the number of spores of Glomus mosseae recovered after storage. However, germinability of the spores decreased from 35% before storage to 10% to 31% during storage, especially under typical ambient room conditions (17% moisture at 24C). Maximum colonization of coast redwood, sierra redwood [Sequoiadendrom giganteum (Lindl.) Buchh.], and incense cedar (Libocedrous decurrens Torr.) was achieved after inoculation with 1 inoculum: 1 potting mix dilution (w/w). However, plant fresh weight was highest following inoculation with a 1 inoculum: 5 potting mix dilution (w/w). Dried inoculum was effective when stored at 24C, or below 10C when moist.


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