Relationship between mycorrhizal activity, burning, and plant productivity in tallgrass prairie

1991 ◽  
Vol 69 (12) ◽  
pp. 2597-2602 ◽  
Author(s):  
S. P. Bentivenga ◽  
B. A. D. Hetrick
Keyword(s):  
Plant Growth ◽  
Tallgrass Prairie ◽  
Mycorrhizal Fungi ◽  
Warm Season ◽  
Arbuscular Mycorrhizal ◽  
Mycorrhizal Colonization ◽  
Prairie Grasses ◽  
Vesicular Arbuscular ◽  
The Impact ◽  
First Time

The impact of benomyl fungicide and spring burning on mycorrhizal activity and plant growth was assessed in tallgrass prairie in Kansas. We report for the first time that the productivity of mycotrophic plants can be reduced by inhibition of indigenous vesicular–arbuscular mycorrhizal fungi under field conditions. A vital stain, nitro blue tetrazolium, used to assess active mycorrhizal colonization, proved to be a more sensitive measure of treatment effects than the cell wall stain, trypan blue. Burning stimulated both plant growth and active mycorrhizal colonization. However, by 32 days after burning no differences in colonization were detected. Our observations support the hypothesis that mycorrhizal fungi play an important role in the growth of warm-season tallgrass prairie grasses and may contribute to enhanced plant growth of warm-season tallgrass prairie grasses and may contribute to enchanced plant growth following spring burning. Key words: burning, benomyl fungicide, phosphorus, tallgrass prairie, VA mycorrhizae, warm-season grasses.

Seasonal and temperature effects on mycorrhizal activity and dependence of cool- and warm-season tallgrass prairie grasses

1992 ◽  
Vol 70 (8) ◽  
pp. 1596-1602 ◽  
Author(s):  
S. P. Bentivenga ◽  
B. A. D. Hetrick
Keyword(s):  
Tallgrass Prairie ◽  
Mycorrhizal Fungi ◽  
Warm Season ◽  
Growing Season ◽  
Cool Temperature ◽  
Cool Season ◽  
Fungal Activity ◽  
Prairie Grasses ◽  
Vesicular Arbuscular ◽  
Warm Season Grasses

Previous research on North American tallgrass prairie grasses has shown that warm-season grasses rely heavily on vesicular–arbuscular mycorrhizal symbiosis, while cool-season grasses are less dependent on the symbiosis (i.e., receive less benefit). This led to the hypothesis that cool-season grasses are less dependent on the symbiosis, because the growth of these plants occurs when mycorrhizal fungi are inactive. Field studies were performed to assess the effect of phenology of cool- and warm-season grasses on mycorrhizal fungal activity and fungal species composition. Mycorrhizal fungal activity in field samples was assessed using the vital stain nitro blue tetrazolium in addition to traditional staining techniques. Mycorrhizal activity was greater in cool-season grasses than in warm-season grasses early (April and May) and late (December) in the growing season, while mycorrhizal activity in roots of the warm-season grasses was greater (compared with cool-season grasses) in midseason (July and August). Active mycorrhizal colonization was relatively high in both groups of grasses late in the growing season, suggesting that mycorrhizal fungi may proliferate internally or may be parasitic at this time. Total Glomales sporulation was generally greater in the rhizosphere of cool-season grasses in June and in the rhizosphere of the warm-season grasses in October. A growth chamber experiment was conducted to examine the effect of temperature on mycorrhizal dependence of cool- and warm-season grasses. For both groups of grasses, mycorrhizal dependence was greatest at the temperature that favored growth of the host. The results suggest that mycorrhizal fungi are active in roots when cool-season grasses are growing and that cool-season grasses may receive benefit from the symbiosis under relatively cool temperature regimes. Key words: cool-season grasses, tallgrass prairie, vesicular–arbuscular mycorrhizae, warm-season grasses.

scholarly journals Detection of Arbuscular Mycorrhizal Fungi in the Roots of Strawberry Plants Fertilized with Organic Bioproducts

2012 ◽  
Vol 77 (1) ◽  
pp. 17-27 ◽  
Author(s):  
Anna Lisek ◽  
Lidia Sas Paszt ◽  
Beata Sumorok
Keyword(s):  
Plant Growth ◽  
Arbuscular Mycorrhizal Fungi ◽  
Nested Pcr ◽  
Mycorrhizal Fungi ◽  
Arbuscular Mycorrhizal ◽  
Am Fungi ◽  
Universal Primers ◽  
Mineral Fertilizers ◽  
Reaction Products ◽  
The Impact

Summary In organic farming, mineral fertilizers are replaced by various preparations to stimulate plant growth and development. Introduction of new biopreparations into horticultural production requires an assessment of their effects on the growth and yielding of plants. Among the important indicators of the impact on plants of beneficial microorganisms contained in bioproducts is determination of their effectiveness in stimulating the growth and yielding of plants. Moreover, confirmation of the presence of arbuscular mycorrhizal (AM) fungi in the roots and plant growth promoting rhizobacteria (PGPR) in the rhizosphere is also necessary. In addition to conventional methods, molecular biology techniques are increasingly used to allow detection and identification of AM fungi in plant roots. The aim of this study was identification and initial taxonomic classification of AM fungi in the roots of ‘Elkat’ strawberry plants fertilized with various biopreparations using the technique of nested PCR. Tests were performed on DNA obtained from the roots of ‘Elkat’ strawberry plants: not fertilized, treated with 10 different biopreparations, or fertilized with NPK. Amplification of the large subunit of ribosomal gene (LSU rDNA) was carried out using universal primers, and then, in the nested PCR reaction, primers specific for the fungi of the genera Glomus, Acaulospora, and Scutellospora were used. Colonization of strawberry roots by arbuscular mycorrhizal fungi was determined on the basis of the presence of DNA fragments of a size corresponding to the types of the fungi tested for. As a result of the analyses, the most reaction products characterizing AM fungi were found in the roots of plants treated with the preparation Florovit Eko. The least fragments characteristic of AM fungi were detected in the roots of plants fertilized with NPK, which confirms the negative impact of mineral fertilizers on the occurrence of mycorrhizal fungi in the roots of strawberry plants. The roots of plants fertilized with Tytanit differed from the control plants by the presence of one of the clusters of fungi of the genus Glomus and by the absence of a cluster of fungi of the genus Scutellospora. In the roots of plants treated with other biopreparations there were reaction products indicating the presence of fungi of the genera Glomus, Scutellospora and Acaulospora, like in the roots of the control plants. The results will be used to assess the suitability of microbiologically enriched biopreparations in horticultural production.

Is cortical root colonization required for carbon transfer to arbuscular mycorrhizal fungi? Evidence from colonization phenotypes and spore production in the reduced mycorrhizal colonization (rmc) mutant of tomato

Botany ◽  
2008 ◽  
Vol 86 (9) ◽  
pp. 1009-1019 ◽  
Author(s):  
Maria Manjarrez ◽  
F. Andrew Smith ◽  
Petra Marschner ◽  
Sally E. Smith
Keyword(s):  
Mycorrhizal Fungi ◽  
Glomus Intraradices ◽  
Arbuscular Mycorrhizal ◽  
Am Fungi ◽  
Mycorrhizal Colonization ◽  
Fungal Mycelium ◽  
Solanum Lycopersicum L ◽  
Carbon Transfer ◽  
External Mycelium ◽  
First Time

For the first time, the phenotypes formed in the reduced mycorrhizal colonization (rmc) Solanum lycopersicum  L. (tomato) mutant with different arbuscular mycorrhizal (AM) fungi were used to explore the potential of different fungal structures to support development of external fungal mycelium and spores. The life cycle of AM fungi with rmc was followed for up to 24 weeks. Results showed that production of external mycelium was slight and transitory for those fungi that did not penetrate the roots of rmc (Pen–) ( Glomus intraradices DAOM181602 and Glomus etunicatum ). For fungi that penetrated the root epidermis and hypodermis (Coi–, Glomus coronatum and Scutellospora calospora ) the mycelium produced varied in size, but was always smaller than with the wild-type 76R. Spores were formed by these fungi with 76R but not with rmc. The only fungus forming a Myc+ phenotype with rmc, G. intraradices WFVAM23, produced as much mycelium with rmc as with 76R. We observed lipid accumulation in hyphae and vesicles in both plant genotypes with this fungus. Mature spores were formed with 76R. However, with rmc, spores remained small and (presumably) immature for up to 24 weeks. We conclude that significant carbon transfer from plant to fungus can occur in Coi– interactions with rmc in which no cortical colonization occurs. We speculate that both carbon transfer and root signals are required for mature spores to be produced.

Seasonal variation in infectivity of vesicular-arbuscular mycorrhizal fungi in relation to plant response to applied phosphorus

Soil Research ◽  
1983 ◽  
Vol 21 (2) ◽  
pp. 207 ◽  
Author(s):  
NS Bolan ◽  
LK Abbott
Keyword(s):  
Seasonal Variation ◽  
Plant Growth ◽  
Soil Sample ◽  
Mycorrhizal Fungi ◽  
Response Curve ◽  
Subterranean Clover ◽  
Arbuscular Mycorrhizal ◽  
Mycorrhizal Infection ◽  
Virgin Forest ◽  
Vesicular Arbuscular

The effect of applied phosphorus on the growth of subterranean clover was studied in a virgin forest soil sample collected in summer and again in spring. The soil sample was used soon after it was collected. The shape of the response curve for plant growth differed greatly in the two experiments. This may be related to the presence of vesicular-arbuscular mycorrhizal infection in plants grown in the soil sample collected in summer and its absence in the soil sample collected in spring.

Mycorrhizal responsiveness of Thuja, Calocedrus, Sequoia, and Sequoiadendron species of western North America

1985 ◽  
Vol 15 (6) ◽  
pp. 1049-1054 ◽  
Author(s):  
J. L. Kough ◽  
Randy Molina ◽  
R. G. Linderman
Keyword(s):  
Arbuscular Mycorrhizal Fungi ◽  
Tree Species ◽  
Mycorrhizal Fungi ◽  
Arbuscular Mycorrhizal ◽  
Mycorrhizal Colonization ◽  
Growth Enhancement ◽  
Vesicular Arbuscular Mycorrhizal Fungi ◽  
Arbuscular Mycorrhizal Colonization ◽  
Vesicular Arbuscular ◽  
Low Phosphorus

Four western conifers inoculated or not inoculated with three species of vesicular–arbuscular mycorrhizal fungi were grown in pasteurized soil and maintained at 11 or 43 ppm phosphorus. Compared with controls, vesicular–arbuscular mycorrhizal colonization increased biomass more of younger than older seedlings. In young seedlings, species with large seeds responded less to phosphate addition or vesicular–arbuscular mycorrhizal colonization than smaller seeded species. Vesicular–arbuscular mycorrhizal seedlings with low phosphorus were always larger than noninoculated low phosphorus controls and comparable in size or larger than nonmycorrhizal controls at moderate phosphorus. Vesicular–arbuscular mycorrhizal plants produced from 100 to 2000% more biomass than noninoculated plants at low phosphorus, and from equality to 500% at moderate phosphorus. Vesicular–arbuscular mycorrhizal fungal species did not differ in plant growth enhancement or root colonization at any seedling age or phosphorus fertility examined. Tree species' responsiveness ranged as follows: Thujaplicata > Sequoiasempervirens > Calocedrusdecurrens > Sequoiadendrongiganteum. Vesicular–arbuscular mycorrhizal fungi enhanced seedling uniformity and size in all the tree species.

Decline of vesicular-arbuscular mycorrhizae in long fallow disorder of field crops and its expression in phosphorus deficiency of sunflower

1987 ◽  
Vol 38 (5) ◽  
pp. 847 ◽  
Author(s):  
JP Thompson
Keyword(s):  
Plant Growth ◽  
Root Length ◽  
Mycorrhizal Fungi ◽  
Root Colonization ◽  
Mycorrhizal Colonization ◽  
Poor Growth ◽  
Plant Weight ◽  
P Deficiency ◽  
Vesicular Arbuscular ◽  
Fallow Soil

Poor growth of crops after long fallows (> 12 months) in cracking clay soils of the northern areas of the Australian grain belt is known as 'long fallow disorder'. Various crop species, including wheat (Triticum aestivum L.), chickpea (Cicer arietinum L.), grain sorghum [Sorghum bicolor (L.) Moench], sudan grass [Sorghum sudanense (Piper) Stapf], sunflower (Helianthus annuus L.), soybean [Glycine max (L.) Merr.] and maize (Zea mays L.), had less root colonization with vesicular-arbuscular mycorrhizal (VAM) fungi and plant weight after long fallows than after short fallows. An experiment was conducted with a phosphorus-deficient soil that had been either fallowed for 3 years or sequentially cropped to cotton, sorghum and sunflower. Cropped soil had more mycorrhizal propagules consisting of intact spores and colonized roots than long fallow soil. In the glasshouse, mycorrhizal colonization of sunflower (cv. Hysun 33) developed quickly in previously cropped soil to peak at 80% of root length at 72 days (flowering), but in long fallow soil it proceeded slowly, attaining 35% of root length at 72 days. Inoculation of long fallow soil with 20% w/w cropped soil resulted in extensive root colonization (89% at 72 days), eliminated P deficiency symptoms and more than doubled plant growth and final P uptake. Inoculation with similar soil treated with gamma radiation to kill propagules of mycorrhizal fungi had no effect on plant growth. Sunflower grew extremely poorly in irradiated soil with considerable leaf necrosis due to P deficiency. Reinoculation with cropped soil resulted In high levels of mycorrhizal colonization and good plant growth. It was concluded that long fallow disorder is caused by a decline in viable propagules of mycorrhizal fungi during fallowing, resulting in poor root colonization and symbiotic effectiveness of a subsequent crop. Fertilizing with phosphorus (50 mg P/kg soil) delayed the development of mycorrhizal colonization, but increased final lengths of colonized roots at 72 days. Zinc fertilizer (15 mg Zn/kg soil) slightly improved mycorrhizal colonization, and basal fertilizer (N, K, S, Ca) substantially improved colonization in long fallow soil inoculated with cropped soil.

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