Two generations of two aphid species (Myzus ascalonicus and M. persicae) were reared on Plantago lanceolata plants, with and without root colonization by the arbuscular mycorrhizal fungus, Glomus intraradices. Life history traits of the aphids measured were nymphal development time, teneral adult weight, growth rate, total fecundity, adult longevity and duration of post-reproductive life. For both aphids in both generations, mycorrhizal colonization increased aphid weight and fecundity, while other traits were unaffected. The increases were consistent between generations. In a second experiment, M. persicae was reared on plants with and without the fungus, under varying N and P regimes. The results of N addition were inconclusive because there was high aphid mortality. However, under P supplementation, positive effects of the mycorrhiza on aphid growth were seen at low and medium P levels, while at high P levels these effects disappeared. The positive effects of mycorrhizal colonization reported here are contrary to the majority of previous studies with chewing insects, which have reported negative effects. A number of possible mechanisms for this apparent discrepancy are discussed.

A series of field and laboratory experiments were conducted to examine whether natural levels of insect herbivory affect the arbuscular mycorrhizal (AM) colonization of two plant species. The plant species were the highly mycorrhizal (mycotrophic) Plantago lanceolata, which suffers small amounts of insect damage continuously over a growing season and the weakly mycorrhizal (non-mycotrophic) Senecio jacobaea, which is frequently subject to rapid and total defoliation by moth larvae. Herbivory was found to reduce AM colonization in P. lanceolata, but had no effect in S. jacobaea. Similarly, AM colonization reduced the level of leaf damage in P. lanceolata, but had no such effect in S. jacobaea. AM fungi were found to increase growth of P. lanceolata, but this effect was only clearly seen when insects were absent. AM fungi reduced the growth of S. jacobaea irrespective of whether insects were present. It is concluded that the reduction of AM fungal colonization by herbivory in P. lanceolata is due to the reduced amount of photosynthate available to the symbiont. This may only become apparent at threshold levels of insect damage and, below these, increased photosynthesis elicited by the mycorrhiza is able to compensate for foliage loss to the insects. However, in S. jacobaea, the mycorrhiza appears to be an aggressive parasite and insect attack only exacerbates the reduction in biomass. In mycotrophic plants, insect herbivores may be responsible for poor functioning of the symbiosis in field conditions and there is a symmetrical interaction between insects and fungi. However, in non-mycotrophic plants, the interaction is strongly asymmetrical, being entirely in favour of the mycorrhiza.

The extent of arbuscular mycorrhizal colonization was assessed in 10 field-collected plant species, representing three annual forbs, three perennial forbs, three perennial grasses and one annual grass. Each root system of each plant was split into four portions, and for each portion, mycorrhizal structures were revealed with epifluorescence microscopy (under which only arbuscules are generally visible) and three commonly used stains (Chlorazol Black E, Acid Fuchsin and Trypan Blue). The aim of the study was not to evaluate the efficacy of each method, but to compare results obtained by each under standard laboratory conditions. The recorded colonization levels of arbuscules, total arbuscular mycorrhizal fungal material and total fungal (arbuscular mycorrhizaljnon-arbuscular mycorrhizal) material differed significantly between visualization methods in a number of species. However, there were also interactions between stain and plant species, indicating that the performance of a stain is dependent on the plant species being examined. In some cases (e.g. Plantago lanceolata), each visualization method produced the same colonization level, while in others (e.g. Dactylis glomerata), each method gave a different result. These data therefore suggest that the level of mycorrhizal colonization recorded in any particular plant species at a particular time is dependent on the technique employed.