Interactions between saprotrophic and ectomycorrhizal fungi have been largely ignored, although their mycelia often share the same microsites. The mycelial systems show general similarity to each other and, although the enzymatic potential of the saprotrophic fungi is generally considered to be higher, the importance of organic nutrient sources to ectomycorrhizal fungi is now widely accepted. In the experiments described here, nutritional interactions involving transfer of elements from one mycelium to the other have been monitored dynamically using radioactive tracers and a non-destructive electronic autoradiography system. Microcosms were used in which mycelial systems of the ectomycorrhizal fungi Suillus variegatus and Paxillus involutus, extending from Pinus sylvestris host plants, were confronted with mycelia of the saprotroph Hypholoma fasciculare extending from wood blocks. The fungi showed a clear morphological confrontation response. The mycorrhizal mycelium often formed dense patches over the Hypholoma mycelia. Up to 25% of the 32P present in the Hypholoma mycelium was captured by the mycorrhizal fungi and translocated to the plant host within 30 d. The transfer of 32P to the saprotroph from labelled mycorrhizal mycelium was one to two orders of magnitude lower. The significance of this transfer as a ‘short cut’ in nutrient cycling is discussed.

A simulation model for the prediction of grassland (Lolium perenne) productivity under conditions of climate change is described and validated for grass growing in the Wageningen Rhizolab, Wageningen, The Netherlands. In this work the model was used to study the impact of different management strategies on the productivity of grassland under present and increased atmospheric CO2 concentrations. In LINGRA-CC simulated key processes are light utilization, leaf formation, leaf elongation, tillering and carbon partitioning. The daily growth rate is determined by the minimum of a sink and a source term. As in a previous model (LINGRA), the potential growth of the sink depends on the mean daily temperature, and can be modified by the effects of the availability of assimilates on tillering. The growth of roots is calculated from the amount of carbohydrates the shoot is unable to utilize when the number or activity of the sinks is small (overflow hypothesis). The main difference between LINGRA and LINGRA-CC is the way the source of assimilates for growth is calculated. Assimilate production depends on intercepted radiation, and a photosynthetic light-use efficiency (LUE) calculated as a function of CO2, temperature, light intensity and the Rubisco concentration of upper leaves. Other differences are that in LINGRA-CC, the specific shoot area for new growth depends on the level of reserves. Data from two independent experiments with L. perenne swards, grown in enclosures at two levels of CO2 during 1994 and 1995, were used to calibrate and validate the model, respectively. The model predicted well the observed amounts of harvested biomass, and the dynamics of the leaf area index, tiller number and specific shoot area. LINGRA-CC was used to study the effects of different combinations of cutting interval and cutting height on biomass production, at ambient (350 μmol mol−1 CO2) and double (700 μmol mol−1 CO2 ) CO2 conditions. Under both ambient and doubled CO2, maximum biomass was produced with cuttings of leaf area index >1, and at cutting intervals of 20 and 17 d for ambient and increased CO2 environments, respectively. Under high CO2 conditions the cutting interval for maximum yield was 15% shorter than at ambient CO2. However, the gain in harvested biomass obtained by reducing the cutting interval by 3 d under high CO2 conditions was negligible.

Numerous authors have attempted to quantify the physical properties of leaves in relation to aspects of leaf ecology, including decomposition, sclerophylly, herbivory, and leaf function and longevity. This paper examines the relative merits of the punch-and-die, tearing and shearing tests for assessing leaf physical properties. We conducted a series of these three mechanical tests on leaves of Solanum laciniatum, and determined the effect of various test parameters on the measurement of fracture properties. For the punch-and-die test, the parameters considered were machine speed, clearance between the punch and the die, edge definition of the punch, and area of the punch. Aspects of the tearing test examined were notch length, end effects, and length-to-width requirements of test strips, and for shearing tests the effects of blade proximity, angle and sharpness were investigated. All the test parameters investigated were found significantly to affect the assessment of leaf-fracture properties. In addition, fracture properties were found to vary significantly within leaves. Some general principles for designing and implementing tests are outlined. This study suggests that while punching and shearing tests are useful means of quantifying leaf fracture properties, the value of the tearing test may be reduced as it is most constrained by the biological nature of the test material.

Ectomycorrhiza formation is a complex developmental process that is still not well understood. To study this process, we identified genetic markers for mycorrhiza development by differential screening of a cDNA library obtained from fully developed Picea abies–Amanita muscaria mycorrhizas. Twenty-three cDNA clones were identified that showed significantly altered gene expression during the ectomycorrhizal interaction. A detailed analysis was performed for two fungal cDNA clones, SC13 and SC25, exhibiting the most pronounced differences. SC13 encodes a protein of 184 amino acid residues that shows no homology with any sequence in databases. It was highly expressed in non-mycorrhizal hyphae, whereas its expression was decreased at least 50-fold in mycorrhizas and fruit bodies. SC25 encodes a protein of 198 residues that shows weak sequence homology with extensin-like plant proteins. The expression of this gene was weak in non-mycorrhizal hyphae but approx. 30-fold higher in mycorrhizas and fruit bodies. Because the expression of both developmentally regulated fungal genes was identical for mycorrhizas and fruit bodies, a common regulation mechanism for both developmental processes is proposed.