The effects of summer drought, dew deposition on leaves and autumn rainfall on plant water relations and diurnal variations of photosynthesis were measured in two evergreen shrubs, rosemary (Rosmarinus officinalis) and lavender (Lavandula stoechas), grown in Mediterranean field conditions. Withholding water for 40 d caused a similar decrease in predawn shoot water potential (ψpd) from c. −0.4 to c. −1.3 MPa in both species, but a 50% decrease in the relative leaf water content in L. stoechas compared with 22% in R. officinalis. A similar decrease in CO2 assimilation rates by c. 75% was observed in water-stressed plants of both species, although L. stoechas showed smaller photosynthesis: stomatal conductance ratio than R. officinalis (35 vs 45 μmol CO2:mol H2O). The relative quantum efficiency of photosystem II photochemistry also decreased by c. 45% at midday in water- stressed plants of both species. Nevertheless, neither L. stoechas nor R. officinalis suffered drought-induced damage to photosystem II, as indicated by the maintenance of the ratio Fv:Fm throughout the experiment, associated with an increase in the carotenoid content per unit of chlorophyll by c. 62% and c. 30%, respectively, in water-stressed plants. Only L. stoechas absorbed dew by leaves. In this species the occurrence of 6 d of dew over a 15-d period improved relative leaf water content by c. 72% and shoot water potential by c. 0.5 MPa throughout the day in water-stressed plants, although the photosynthetic capacity was not recovered until the occurrence of autumn rainfall. The ability of leaves to absorb dew allowed L. stoechas to restore plant water status, which is especially relevant in plants exposed to prolonged drought.

In four field and glasshouse experiments designed to alter the supply of resources through manipulation of nutrients, root tissue, leaf area and fruit number in Alliaria petiolata (Brassicaceae), more than 99% of ovules per plant showed signs of fertilization, suggesting that seed production in this plant was not pollen limited. However, in all treatments a significant proportion of fruits and seeds did not develop to maturity. Total fruit and seed production did not differ significantly from controls when plants were given nutrient supplements at flowering. Removal of 50–75% of the root tissue in 1-yr-old plants significantly reduced fruit set, but had no effect on individual seed development. Removal of cauline leaves significantly reduced most measures of fruit and seed production, suggesting that current photosynthate is critical for fruit and seed filling. Seed maturation was significantly affected by both fruit position within an infructescence and ovule position within a fruit. Basally located fruits and ovules (within fruits) developed more mature seeds than distally positioned fruits and ovules. Plants responded to removal of basal fruits by re-allocating resources to distal fruits that would normally have aborted. Our results suggest that fruits and seeds act as reproductive sinks competing for parental photosynthate. Patterns of resource allocation within infructescences and fruits were also modified by our experiments.

In vesicular–arbuscular mycorrhizal symbioses, specialized fungal structures (the arbuscules) are formed which are in intimate contact with plant root cortical cells. It is assumed that these arbuscules are the major sites of solute transfer between the plant and fungus, but there have been no studies that definitively show the extent or types of transfer processes that occur in this structure. Phosphate is one of the major nutrients that is acquired by mycorrhizal fungi and transferred to plants. In this study a single Lycopersicon esculentum cDNA was cloned and shown to be identical to LePT1, a previously cloned inorganic-phosphate transporter. Expression studies revealed that LePT1 transcript levels remained constant in mycorrhizal plants, but increased in phosphate-starved, non-mycorrhizal plants. Localization of the LePT1 transcript by in situ hybridization showed that this gene is highly expressed in arbuscule-containing cortical cells in mycorrhizal plants. In non-mycorrhizal plants LePT1 expression was localized to the stele and cortex. The expression studies suggest that this transporter is involved in phosphate nutrition of L. esculentum and its localization in cells that contain arbuscules indicate that it may be the mechanism used by the plant to take up phosphate that is effluxed across the fungal plasma membrane of the arbuscule. Based on our findings and those of others, an integrated model of inorganic phosphate uptake and transfer in mycorrhizal and non-mycorrhizal plants is presented.

The effects of partial defoliation on photosynthesis, whole-seedling carbon allocation, partitioning and growth were studied for two species with contrasting foliar traits. Field-grown seedlings of deciduous Japanese larch (Larix leptolepis) and evergreen red pine (Pinus resinosa) were defoliated by hand in early summer for 2 consecutive years. In the first year (1990), seedlings were defoliated by removing the distal 0, 25, 50 or 75% of each needle. In the second year (1991), seedlings were defoliated either 0 or 50%, regardless of previous defoliation treatments. Defoliation had little effect on photosynthesis and starch concentration in whole seedlings of either species in the first year. In the second year, photosynthesis increased in both species in response to the 1991 defoliation treatment, and in red pine also increased in response to the 1990 defoliation treatment. Further, in 1991 both larch and pine had decreased whole-seedling total non-structural carbohydrate concentrations in all seedlings that were defoliated at least once over the 2-yr period. This decrease was noted mostly in the starch component of the non-structural carbohydrates, and was similar in both species. In 1991, biomass was similarly decreased in both species in response to 1991 defoliation. Both species showed overcompensation in total and component biomass in seedlings defoliated by 25% in 1990. Overall, the results do not support the widely held belief that evergreen trees are substantially more affected than deciduous trees by defoliation.

Under ecologically realistic environmental conditions, the water-use efficiency (WUE) of Peperomia scandens, a CAM plant, was higher than that of the C3 congener P. obtusifolia. This difference has been attributed to differences in stomatal activity between C3 and CAM plants, coupled with differences in the evaporative demand of the atmosphere during which the stomata are open. This explanation has apparently not, however, been experimentally tested. Thus, WUEs were compared in these species in two experiments in which the atmospheric evaporative demand was identical (or nearly so) during the period of stomatal opening (i.e. during the night for the CAM plant and during the day for the C3 species). In both experiments, the WUE of the CAM species was higher than that of the C3 species. These results suggest that factors other than differences in atmospheric environmental conditions must also be responsible for the observed differences in WUE. Because CO2 uptake rates of the CAM species were substantially lower than those of the C3 species, the lower WUE in the CAM species resulted primarily from lower transpiration rates. Lower rates of water loss in P. scandens, relative to rates in P. obtusifolia, were ascribed, in part, to lower stomatal densities. Thus, leaf morphological differences, in addition to differences in atmospheric evaporative demand, help to explain the high WUE typically measured in CAM plants.

Bulbous rush (Juncus bulbosus) initiates plant colonization in extremely acid lakes resulting from coal mining operations. Various analytical techniques (methylene blue/agar method, Ti3+-citrate solution) X-ray diffraction (XRD), scanning electron microscopy (SEM), and Energy-dispersive X-ray (EDX) were used to assess the mechanisms and strategies employed by J. bulbosus to overcome the extreme conditions. The plant releases oxygen into the rhizosphere in turn increasing the redox potential and inducing iron oxide plaque formation. XRD showed that the iron oxide of the plaque is mainly goethite that has been developed in the presence of CO2; SEM showed that there is a micro-space between the roots and sand grains which is inhabited by microorganisms. Furthermore, SEM-EDX studies on internal iron distribution demonstrate that iron toxicity is delayed by the physiological and biochemical structure of the plant. It is suggested that J. bulbosus uses a variety of mechanisms and strategies (morphological, physiological and biochemical adaptation) which are mainly complementary and which interact with each other to help J. bulbosus to manage its growth and survival in an extreme environment.

Seedlings of the annual grass Vulpia ciliata ssp. ambigua were grown in sterilized sand with a dark septate root fungus, Phialophora graminicola, which had been isolated from a natural population of the grass. Tiller number and shoot, root and total biomass of seedlings grown with P. graminicola were enhanced relative to uninoculated control plants in a growth room and a glasshouse experiment. Root length of seedlings grown with P. graminicola was significantly increased, but no effects of the fungus on root diameter, number of root hairs or specific root length were recorded. Root nitrogen content and shoot, root and total phosphorus contents of seedlings grown with the fungus were enhanced, but shoot nitrogen concentration of these plants was reduced. Shoot biomass and specific root length of inoculated plants were positively associated with the number of P. graminicola colonies re-isolated from roots. These data indicate that P. graminicola acts as a beneficial associate of V. ciliata ssp. ambigua seedlings under controlled conditions.

Resistance to complete submergence was tested in three Rumex species that occur in the Dutch river forelands. The species differ in both habitat and life history characteristics. The annual or biennial R. maritimus and the biennial or short lived perennial R. palustris grow on frequently flooded mud flats of low elevation, while the perennial R. thyrsiflorus can be found on dykes and river dunes that are seldom flooded. The flooding characteristics of the habitats of the three species were determined. These data were used to design experiments to determine the survival and biomass development of the three species during submergence and the influence of plant size and light level on these parameters. It was shown in all three species that plants submerged during daytime were much more resistant to flooding than those submerged at night. This is most probably due to the generation of oxygen or carbohydrates by underwater photosynthesis. Mature plants of the three species showed higher survival after submergence than juvenile plants, which might be caused by higher carbohydrate levels in the taproots of mature plants. In addition, the three species clearly differed in survival and biomass development during submergence. Rumex thyrsiflorus, the species least subjected to flooding, is least tolerant to complete submergence. Rumex maritimus, which can avoid the floods by having a short life cycle, is less tolerant to submergence than R. palustris, which has to survive the floods as a vegetative plant. It was noted that some plants that survived the flooding period itself, still died in the following period of drained conditions, possibly due to post-anoxic injury.

Concentrations of starch in roots of seeder species of Erica from the Cape Floristic Region, South Africa were found to be considerably less than in resprouters. Shoot starch was highly variable but mean values were similar in both seeder and resprouter species of Erica. Three distinct patterns of starch storage in roots were recognized. All seeder species fell within definitions of Categories 1 (narrow major and minor parenchymatous rays, one to two cells wide with no inter-ray storage) or 2 (thick major rays up to seven cells wide and thin minor rays with small amounts of inter-ray storage) whereas resprouter species were consistently within Categories 2 or 3 (broad major and minor rays, up to eight cells wide and conspicuous inter-ray starch storage). Results are discussed in light of similar studies of the related Epacridaceae. ‘Mixed’ species (i.e. with seeder or resprouter individuals present, often in distinct populations) were always classified as belonging to Category 2. Studies of populations of three ‘mixed’ species confirmed that seeder forms had consistently lower amounts of root starch than resprouters. Rays of xylem parenchyma were the main sites for starch storage in roots of both seeders and resprouters and greater proportions of cross-sectional area of roots were consistently devoted to such storage tissues in resprouter forms of the three ‘mixed’ species. Analyses of a number of seeder and resprouter Erica coccinea populations showed that differences in amounts of realised and potential root starch storage are best explained by the effect of regeneration behaviour rather than by among-population variability.

The natural abundance of 13C and 15N was measured in basidiocarps of at least 115 species in 88 genera of ectomycorrhizal, wood-decomposing and litter-decomposing fungi from Japan and Malaysia. The natural abundance of 13C and 15N was also measured in leaves, litter, soil and wood from three different sites. 15N and 13C were enriched in ectomycorrhizal and wood-decomposing fungi, respectively, relative to their substrates. Ectomycorrhizal and wood-decomposing fungi could be distinguished on the basis of their δ13C and δ15N signatures. Although there was high variability in the isotopic composition of fungi, the following isotope- enrichment factors (ε, mean±SD) of the fungi relative to substrates were observed:

εectomycorrhizal fungi/litter = 6.1±0.4‰ 15N

εectomycorrhizal fungi/wood = 1.4±0.8‰ 13C

εwood-decomposing fungi/wood = −0.6±0.7‰ 15N

εwood-decomposing fungi/wood = 3.5±0.9‰ 13C

The basis of isotope fractionation in C metabolism from wood to wood-decomposing fungus is discussed.

A systematic survey of the endophytic assemblages of Quercus ilex in central Spain has been performed, with the goal of evaluating the importance of geographical and seasonal factors on these fungal communities. Four sampling sites were selected; one of them was sampled twice, in the spring and the autumn. The collected plant material consisted of bark, twigs and leaves from eight trees per site. Fungal strains were isolated with the use of a surface-sterilization method with sodium hypochlorite. A total of 2921 fungal strains grouped into 149 ‘species’ or morphological types were recovered. The 10 dominant species, with isolation frequencies >1.5%, were Pyrenochaeta sp., Periconiella anamorph of Biscogniauxia mediterranea (De Not.) Kuntze, Pseudonectria sp., Cryptosporiopsis quercina Petrak, Alternaria alternata (Fr:) Keissl., two undetermined coelomycetes, Penicillium funiculosum Thom, Diplodia mutila Fr. apud Mont. and Ascochyta sp. Medians of fungal species per tree were significantly different among the sampled sites. The isolation frequencies of the dominant species, as well as other less frequent species, were significantly dependent on the sampling site. The degree of endophytic infection and the diversity of fungal species were significantly higher in the spring. The frequencies of all dominant species at one of the sites depended significantly on the season, except for C. quercina, Acremonium sclerotigenum (F & V Moreau ex Valenta) Gams. and D. mutila. Cluster analysis of the whole endophytic mycoflora of the sampled trees suggested that the geographical factor affects the endophytic distribution patterns more significantly than the seasonal factor.

It is generally accepted that larger seeds give rise to seedlings with better performance. On the other hand, the size that a seed reaches is genetically determined by at least two different traits ; the genetic variability of the developing embryo and the genetic variability of the maternal plant. Thus, the relative contributions of these two traits affect seedling performance by influencing seed size. In this paper, I investigate the effect of seed size on seedling performance in the Scots pine (Pinus sylvestris). From eight maternal plants, 50 seeds were planted in each of two soil types (800 seeds in total), and seedling performance was monitored for 1 yr. Seed mass proved to be highly constant within maternal plants. Soil type influenced emergence and survival; however, the effect of soil type differed depending on maternal origin. Seed mass was positively correlated with seedling emergence, although this relationship was not found for seedling survival or date of emergence. The initial growth of the shoot was also positively correlated with seed mass. However, after one growing season, seed mass had no effect on seedling performance, which depended exclusively on maternal origin. Nevertheless, the mean mass of seeds produced by plants was positively correlated with mean values of growth parameters. Thus, first-year seedling performance seems to be a maternal trait indirectly associated with seed size.

Afrothismia winkleri develops fleshy rhizomes, densely covered with small root tubercles, narrowing to filiform roots with age. The exclusively intracellular mycorrhizal fungus has distinct morphologies in different tissues of the plant. In the filiform root the hyphae grow straight and vesicles are borne on short hyphal stalks. The straight hyphae are present in the epidermis of the root tubercles, but change to loosely coiled and swollen hyphae in the rhizome tissue. No penetration from epidermis to root cortex was found. From the rhizome, a separating cell layer permits only one or rarely two hyphal penetrations into the cortex of each root tubercle. The hyphae proceed apically within the root hypodermis in a spiral row of distinctively coiled hyphae, branches of which colonize the inner root cortex. In the inner root cortex the hyphal coils degenerate to amorphous clumps. In older roots the cortex itself also deteriorates, but epidermis, hypodermis, endodermis and central cylinder persist. The mycorrhizal pattern in A. winkleri is interpreted as an elaborate exploitation system whereby the fungus provides carbon and nutrients to the plant and, simultaneously but spatially distinct, its hyphae are used to translocate and store the matter within the plant. Several features indicate that the endophyte is an arbuscular mycorrhizal fungus.

Binucleate Rhizoctonia endophytes from the roots of nursery-grown Pinus sylvestris (Scots pine) seedlings and the orchid Goodyera repens from Scots pine forests were characterized on the basis of morphological characters, anastomosis group membership and PCR-assisted ribosomal DNA fingerprinting. Common hyphal and colony morphological traits displayed by the Finnish binucleate Rhizoctonia isolates and a range of Canadian orchid root endophytes enabled them to be placed in the anamorphic genus Ceratorhiza. Five main anastomosis groups were identified and included groups that contained different combinations of Scots pine, G. repens and Canadian Ceratorhiza spp. isolates. Two Scots pine root endophytes anastomosed with a phytopathogenic Japanese tester isolate, confirming their membership of anastomosis group I, which is known to include the teleomorphic species Ceratobasidium cornigerum. Hierarchical cluster analysis of RFLPs in the internal transcribed spacer of ribosomal DNA enabled the division of isolates into one of five RFLP groups. The RFLP and anastomosis groupings were closely correlated; isolates within each of four RFLP groups, which shared 100% RFLP identity, anastomosed in the cross-pairing anastomosis group tests. However, all represented different vegetatively compatible populations (clones) because the diagnostic killing reaction, a cellular vegetative incompatibility response, was identified at hyphal fusion junctions. These findings indicate a high degree of intraspecific variation within Ceratobasidium cornigerum, which includes isolates able to enter into either mutualistic or pathogenic root association with susceptible host plants. The common anastomosis group/RFLP groupings identified also strongly support the hypothesis that conifer tree roots can act as large inoculum reservoirs for these orchid endophytes, allowing the development of inter-plant connections, via commonly shared hyphal linkages, in boreal forest ecosystems.

A cDNA coding for a fungal amino acid transporter (AmAAP1) was identified from Amanita muscaria ectomycorrhizas. The transporter gene was expressed at a basal level under all conditions investigated, but its expression was enhanced 10-fold in the absence of a N source utilized by the fungus. Nitrate was not a suitable N source for A. muscaria and resulted in maximal AmAAP1 expression. The expression of AmAAP1 in a yeast mutant revealed its function as a high-affinity amino acid transporter with a broad substrate spectrum. AmAAP1 takes up all investigated amino acids with Km values between 22 μM for histidine and up to 100 μM for proline. Gene expression and amino acid uptake data together indicate two main functions for AmAAP1: uptake of amino acids from soil for fungal nutrition, and prevention of an amino acid loss by hyphal leakage in the absence of a suitable N source.

Roots of clonal birches (Betula pendula) were inoculated with the ectomycorrhizal fungi Paxillus involutus (isolates P0 and Mi) and Hebeloma cylindrosporum (strains D1 and D105). These fungi showed different rates of mycorrhiza formation in vitro. Mature mycorrhizas were obtained after only 2–4 d with H. cylindrosporum, whereas 6–8 d were necessary with P. involutus isolate P0, and P. involutus isolate Mi was not able to form mature mycorrhiza during the 10 d of the experiment. Temporal changes in PAL activity and the expression of genes encoding intracellular pathogenesis-related proteins were followed after inoculating birch roots with these fungi. Transient increase of PAL activity, and transient induction of expression of the wound-inducible Bet v1-SC1 gene, were observed in roots challenged with both H. cylindrosporum strains and the P. involutus isolate P0. These changes were found to coincide with hyphal penetration between root cells during Hartig net formation, and were never observed in roots inoculated with the poorly aggressive P. involutus isolate Mi. Examination of mycorrhizal root sections under u.v. light indicated the presence of phenolic compounds in the host cell walls at the vicinity of the Hartig net. These results strongly suggest that hyphal penetration between the root cells triggers a transient defence response which, in turn, could limit Hartig net formation to the outer layer of the root cortex.

Two arbuscular mycorrhizal fungi, Scutellospora calospora and Glomus sp. ‘City Beach’, were grown in soil conditions suitable for colonization of Allium porrum. Effects on plant growth and phosphate uptake were examined. Isolates of S. calospora (including the one used here) have been shown by others to vary in their stimulation of plant growth, and appear to be inefficient in the transfer of P from the fungus to the host. Our hypothesis was that such isolates of S. calospora may be more aggressive colonizers than other fungi, thus preventing growth increases or producing strong growth depressions in the host plant. In fact, inoculation with either fungus increased growth of plants in their respective soils both low in P (P0) and with added P (P1) by 42 d. The effect on growth due to mycorrhizal symbiosis (i.e. mycorrhizal growth response, % MGR) at 42 d was higher in plants grown in P0 soil. Plants colonized by Glomus sp. ‘City Beach’ had a greater % MGR than plants colonized by S. calospora. Both fungi colonized plants to high levels. The percentage of root length colonized was higher in P0 soil than in P1 soil at 21 d. The internal development of S. calospora appeared less affected by addition of P than Glomus sp. ‘City Beach’ at the early harvests. Formation of arbuscules followed the same trends as total colonization. Shoot P concentration was significantly higher in mycorrhizal plants than in non-mycorrhizal plants, by 21 d in P1 soil and by 28 d in P0 soil. Different percentage responses to added P based on total plant dry weight (% PGR) were observed at 28 and 42 d between the plants colonized by the two fungi. The increased P content due to mycorrhizal colonization (% MPR) differed with soil P. For both fungi grown in their respective soils, the response was greater in plants grown in P0 soil. Although the isolate of S. calospora used is an aggressive arbuscular mycorrhizal fungus with some hosts, it promotes a strong positive plant growth response in A. porrum after a mild initial growth depression.

The population dynamics of perennial crop plants are influenced by numerous factors, including management practices. Conditions in the field vary from year to year, and matrix population models are useful for evaluating population behaviour in relation to environmental variability. In Missouri, the stand persistence of birdsfoot trefoil (Lotus corniculatus), a perennial legume, is often limited by disease and poor seed production. A stage-based, matrix population model was developed to evaluate the population dynamics of birdsfoot trefoil in relation to clipping treatment. The plant growth stages represented in the model were seeds, seedlings, mature vegetative and reproductive plants. Two phases of population growth were evaluated in clipped and unclipped stands. Establishment-phase populations were characterized by relatively high mortality and low reproduction. Elasticity analysis indicated that growth of these populations was most sensitive to the survival of vegetative plants. Mature vegetative plants and seeds comprised the majority of surviving individuals in clipped and unclipped populations, respectively; however, establishment-phase populations under both management treatments tended toward extinction. Populations in the post-establishment phase of growth were characterized by relatively low mortality and high reproduction. Population growth in this phase of growth was most sensitive to seed production, and most individuals in these populations were at the seed stage.

This study investigated the relationships between ericoid mycorrhizal endophytes of the Ericaceae (Northern Hemisphere) and the Epacridaceae (Australia). Over 200 fungi were isolated from the roots of two species of Epacridaceae from Victoria, Australia. The isolates were divided into 12 groups by morphology on quarter-strength potato dextrose agar. All were slow-growing and most were dematiaceous, but groups varied from white through pink to dark olive. The ITS1–5.8S–ITS2 ribosomal DNA was amplified and sequenced from eight isolates, forming typical ericoid mycorrhizal morphology in Epacris impressa and one nonmycorrhizal isolate. Sequences were compared, by using similarities and maximum-parsimony analysis, with those of Hymenoscyphus ericae (Leotiales) and Oidiodendron species (Hyphomycetes), the most common endophytes of the Ericaceae. Maximum-parsimony analysis produced four clusters: (1) all Oidiodendron species (at least 90% similarity); (2) all five Victorian dark grey-olive isolates (at least 96% similarity); (3) one Victorian isolate and Cistella grevillei (88% similarity); (4) two light-coloured Victorian isolates and H. ericae (81% similarity). This suggests that these isolates from the Epacridaceae do not belong to the same species as those forming ericoid mycorrhiza in the Ericaceae.

Individual arbuscular mycorrhizal fungi can differ markedly in their ability to improve the phosphate nutrition and growth of host plants. In particular, Scutellospora calospora is relatively ineffective with some hosts and a growth depression is often observed. We have examined the abilities of S. calospora and Glomus sp. ‘City Beach’ strain WUM 16, grown in soils which promote extensive mycorrhizal colonization, to transfer phosphate (P) to Allium porrum. Phosphate uptake from the low-P soils (P0) was compared with uptake from soils amended with extra P (P1). In order to relate P transfer to physiological characteristics of the two fungi, inflow of P via fungus to the plant was combined with the surface areas of intercellular hyphae and arbuscules (symbiotic interfaces) to calculate the amount of P transferred per unit area of interface (P fluxes). ‘Hyphal inflows’ and ‘hyphal fluxes’ were also calculated on the assumption that P uptake by the plant was the same in mycorrhizal and equivalent non-mycorrhizal (NM) plants (the validity of this assumption is discussed). With both soil P treatments, P was taken up by plants colonized by both mycorrhizal fungi to a greater extent than by the equivalent NM controls. Hyphal inflows to plants in P0 soil that were colonized by Glomus sp. ‘City Beach’ were greatest from 14–21 d and decreased at later harvests. With P1 soil the inflow via Glomus sp. ‘City Beach’ peaked at a very high value at 21–28 d. Hyphal inflows into plants in P0 soil that were colonized by S. calospora increased throughout the experiment, and with P1 soil they remained steady at high values. With both fungi, the surface areas of the symbiotic interfaces increased greatly after 14 d, and generally there was little effect of higher soil P. With P0 soil, Glomus sp. ‘City Beach’ showed no significant differences in the ratio of surface areas of the two interfaces over the course of the experiment. Scutellospora calospora tended to produce a lower percentage of interfacial area contributed by arbuscules. With the mycorrhizal plants growing in their respective soils, there appeared no consistent differences between the two fungi with respect to fluxes of P across the interfaces. With P0 soil, fluxes via Glomus sp. ‘City Beach’ were initially higher than those via S. calospora, but later they were higher with S. calospora. With P1 soil the only difference was the 28–42-d period, when Glomus sp. ‘City Beach’ produced the higher flux (reflecting the low surface area at the time). The results show that relative inefficiency of S. calospora in its ability to transfer P, as reported by others, may result from different environmental conditions, use of different hosts, or even of different fungal isolates (strains).