A

A. D. Robson

University of Bristol

ORCID: 0000-0003-3338-2626

Publishes on Legume Nitrogen Fixing Symbiosis, Mycorrhizal Fungi and Plant Interactions, Plant Micronutrient Interactions and Effects. 158 papers and 9.6k citations.

158Publications
9.6kTotal Citations

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Top publicationsby citations

External hyphae of vesicular‐arbuscular mycorrhizal fungi associated with <i>Trifolium subterraneum</i> L.
Cited by 919Open Access

summary Variation among VA mycorrhizal fungi in their ability to enhance phosphorus uptake and plant growth could be due to differences in the length, distribution and phosphorus uptake of external hyphae. Trifolium subterraneum L. was grown in a sandy soil in association with the VA mycorrhizal fungi Acaulospora laevis Gerdemann &amp; Trappe, Glomus sp., Scutellospora calospora (Nicol. &amp; Gerd.) Walker &amp; Sanders or left uninoculated. When mycorrhizas had become well established, plants were transferred to a two‐compartment system, where root growth into a hyphal compartment was restricted by a fine nylon mesh. Spread of hyphae into the hyphal compartment was monitored by sequential sampling of soil cores at different distances from the root compartment. Plants were harvested at three times. The spread of hyphae differed between fungi. The length density of hyphae of S. calospora declined approximately exponentially with increasing distance from the roots, whereas A. laevis maintained a plateau of constant hyphal density up to 7 and 11 cm from the roots after 28 and 47 d, respectively. Glomus sp. had an intermediate pattern of spread with a plateau closest to the roots followed by an exponential decline. The average rate of hyphal spread (mm d −1 ) was 3.1 for A. laevis but only 0.7–0.8 for Glomus sp. and S. calospora. In addition to its more extensive hyphal spread, A. laevis produced the largest increases in phosphorus uptake and plant growth. All mycorrhizal plants had a larger phosphorus inflow than the non‐mycorrhizal controls, but the phosphorus inflow per unit mycorrhizal root length was 25.3 times as high with A. laevis as with the two other fungi. These differences between the fungi became even more pronounced when the phosphorus inflow was expressed on the basis of hyphal length. This work indicates that the efficiency of phosphorus uptake by a VA mycorrhizal fungus is strongly affected by its spatial distribution of hyphae in the soil, and possibly also by differences in capacity for uptake by unit length of hypha.

External hyphae of vesicular—arbuscular mycorrhizal fungi associated with <i>Trifolium subterraneum</i> L.
Cited by 649Open Access

summary Phosphorus transport by hyphae of the three VA mycorrhizal fungi, Acaulospora laevis Gerdemann &amp; Trappe, Glomus sp. and Scutellospora calospora (Nicol. &amp; Gerd.) Walker &amp; Sanders, associated with Trifolium subterraneum L. was investigated by means of radiotracer techniques. Plants with roots heavily colonized by each mycorrhizal fungus were transplanted to two‐compartment systems, where a hyphal compartment was separated from the main compartment by a fine mesh preventing root penetration. The hyphal compartment contained layers of 32 P‐labelled soil, which were placed at 0, 1, 2.5, 4.5 or 7 cm from the root compartment. A time‐course study over 37 d showed that Glomus sp. transported most 32 P to shoots over soil‐root distances shorter than 1 cm. In contrast, A. laevis transported most 32 P to shoots over soil–root distances longer than 1 cm. This ability of A. laevis to transport phosphorus over longer distances than Glomus sp. parallels previous observations that hyphae of A. laevis spread faster and further in soil than hyphae of the Glomus sp. Scutellospora calospora transported much less 32 P to plants, but accumulated more 32 P in its hyphae, than the two other fungi. The higher specific radioactivity in the hyphae of S. calospora than of A. laevis and Glomus sp. indicated a retarded translocation of 32 P in its hyphae or retarded transfer of 32 P across its interface with the host. However, the poor phosphorus transport by S. calospora might also have resulted from its reaction to root trimming at transplanting; percentage root colonization by S. calospora decreased markedly after transplanting to the labelling system.