Quantitative and reproducible information concerning the development o
f the extraradical mycelium of arbuscular mycorrhizal fungi (AMF) is l
acking due to the difficulties in extracting, identifying and estimati
ng hyphal lengths. In this study, using a rhizobox growth system, the
lengths of hyphae of AMF estimated using an image analysis system were
not significantly different from data obtained by a trained observer
using a modified grid-line intersect method. The assessment of lengths
of hyphae on membrane filters or slides was, however, much quicker us
ing image analysis, and allowed the complete sample to be quantified,
unlike the grid-line method where a limited number of fields of view a
re assessed. The image analysis procedure is objective, observer-indep
endent and less laborious than the manual method of assessment. Of the
four different methods of sample preparation compared, membrane filte
r methods were found to be the most appropriate for quantitative sampl
ing from three non-soil substrates. Glomus monosporum (UKC M3) produce
d twice as much extraradical mycelium and hyphal length per centimetre
of colonised root than G. geosporum (BEG 11) on both leek and linseed
in a durite sand at final harvest (63 days). Both AMF also produced m
ore hyphal length per centimetre of colonised root on linseed than on
leek. The spatial distribution of both AMF, however, was similar in du
rite sand and no correlation with levels of NaHCO3-extractable phospho
rus was noted. In a third experiment, with G. manihotis (UKC INDO-1) c
olonising a tropical forage legume, Pueraria phaseoloides, in two othe
r growth substrates, a different pattern of development of the extrara
dical mycelium was observed. Because of a higher content of particulat
e matter, which collected on the membrane filters, the extraction tech
nique had to be modified to give optimal performance of the image anal
ysis system.