We studied carbon and nitrogen allocation in mycorrhizal and non-mycorrhizal Scots pine (Pinus sylvestris L.) seedlings grown in a semi-hydroponic system with nitrogen as the growth limiting factor. Three ectomycorrhizal fungi were compared: one pioneer species (Thelephora terrestris Ehrh.: Fr.) and two late-stage fungi (Suillus bovinus (L.: Fr.) O. Kuntze, and Scleroderma citrinum Pers.). By g...

Nursery grown seedlings of Pinus virginiana with infection by Pisolithus tinctorius (Pt) versus seedlings with naturally occurring mycorrhizae were used in greenhouse experiments to determine the influence of mycorrhizae on manganese and zinc uptake and distribution in seedlings. Unamended Pt mycorrhizal seedlings and those treated with 48.0 mg Mn/pot over a 2-week period accumulated significan...

Spores density and mycorrhizal colonization were studied in twenty-five rhizosphere samples of some selected soils and plant roots from fertile and marginal soils of North West Frontier Province of Pakistan. All tested plants are considered to be mycorrhizal plants. Highest number of mycorrhizal spores was found in Potatoes, Barley, rice and chickpea (>4000 spores kgG soil) in fertile soils. Fi...

Inoculation of the grapevine (Vitis amurensis Rupr.) with the arbuscular mycorrhizal (AM) fungus Glomus versiforme significantly increased resistance against the root-knot nematode (RKN) Meloidogyne incognita. Studies using relative quantitative reverse transcription-PCR (RQRT-PCR) analysis of grapevine root inoculation with the AM fungus revealed an up-regulation of VCH3 transcripts. This incr...

Currently in Western Australia, phosphite is being used to contain the root and collar rot pathogen, Phytophthora cinnamomi, in native plant communities. There have been reports of negative effects of phosphite on arbuscular mycorrhiza (AM), so there are concerns that it may have a deleterious effect on other mycorrhizal fungi. Two glasshouse experiments were undertaken to determine the impact ...

Mycorrhizal status of the host plant is often ignored in studies on plant-herbivore interactions, but mycorrhizal colonization is known to induce many morphological, physiological, and biochemical changes in host plants, which in turn may alter plant quality as a host for insect herbivores. Both positive and negative effects of mycorrhizal colonization of the host plant on performance and densi...

A number of studies have shown that an association with mycorrhizal fungi can alter the outcome of interactions between plants and their enemies. While the directions of these effects vary, their strength suggests the need for greater attention to multispecies interactions among plant enemies, plants, and mycorrhizal fungi. We recognize that mycorrhizal fungi could effect plant enemies by impro...

Mycorrhizal soybean (Glycine max L. Merr. var. Harosoy-63) plants have lower resistances to water transport than nonmy-corrhizal plants after 4.5 weeks of growth. Although resistances of whole plants differ by 40%, there were no differences in the resistances of stems plus leaves, indicating that the major effect of the mycorrhizae was to reduce the resistance of the roots. Since the fungitoxic...

In a first experiment of soil contaminated with 137Cs, inoculation with a mixture of arbuscular mycorrhizae enhanced the uptake of 137Cs by leek under greenhouse conditions, while no effect on the uptake by ryegrass was observed. The mycorrhizal infection frequency in leek was independent of whether the 137Cs-contaminated soil was inoculated with mycorrhizal spores or not. The lack of mycorrhiz...

Podocarps are often found on lownutrient soils and further exacerbate nutrient limitation through the production of recalcitrant litter. Understanding podocarp ecology therefore depends on understanding the root adaptations of podocarps to obtain nutrients. The roots of podocarps are heterorhizic (having two root forms) with abundant spherical determinate short roots, a unique form of largely u...