The Paxillus involutus (Fries) Karsten–Betula pendula Roth association was studied during the early stages of formation. Cytological studies revealed fungal colonization behind the root cap and gradually around the entire root apex. Ultrastructural investigations were carried out and insoluble polysaccharide distribution was followed. The density of starch grains increased in plant cells especially after 4 d of contact between the two partners, but later on decreased strongly in the root cap. Large amounts of glycogen were revealed in the hyphae in certain mycorrhizal regions after 6 d of contact: in the Hartig net, in the inner sheath but only near the net, and all along the outer sheath surrounding the mycorrhiza. Thickenings of the epidermal cell walls were detected as early as 2 d after contact and then varied according to the distance from the root tip. Such polysaccharide distributions are assumed to show a transfer of carbohydrates from the root to the fungus and are discussed in terms of carbon requirements for both partners.

This light- and electron-microscope study of four species of Sphagnum reveals that stem elongation involves meristematic activities unique to the group and hitherto unrecognized. The internal tissue of the mature stem arises by the concerted activity of an apical (primary) and a subapical (secondary) meristem. The primary meristem comprises the immediate derivatives of the single apical cell. Following a small number of divisions, the primary derivatives differentiate into highly vacuolate parenchymatous cells with a storied arrangement. Subsequently, the large vacuoles are replaced by numerous small vacuoles and the cells then divide repeatedly, by transverse septa, producing files of about nine short cells. Finally, ninefold elongation of these secondary cells is responsible for extension growth of the main stem below the mature capitulum. An early step in primary differentiation is the confinement of pre-existing plasmodesmata to distinct pitted areas. Further enlargement of the cells during primary and secondary differentiation involves the thickening of non-pitted wall areas, followed by expansion and thinning out, while the pitted areas remain virtually unchanged. A cortical array of microtubules is regularly found in association with non-pitted wall areas, while the unexpanded pitted areas are associated with smooth endoplasmic reticulum showing continuity with desmotubules. Though sharing much the same cytology as the conducting cells in bryoid mosses, in terms of their development the central stem cells in Sphagnum are not homologous with those of other mosses. The unique mode of stem development may be an important factor in the ecological success of Sphagnum.

The ability of four species of vesicular–arbuscular mycorrhizal (VAM) fungi to increase phosphorus uptake and growth of clover plants (Trifolium subterraneum L.) at different levels of soil compaction and P application was studied in a pot experiment. Dry matter in the shoots and roots of clover plants decreased with increasing soil compaction. Colonization by Glomus intraradices Schenck & Smith and Glomus sp. City Beach WUM16 increased plant growth and P uptake up to a bulk density of 1·60 Mg m−3, although the response was smaller as soil compaction was increased. Glomus etunicatum Becker & Gerdeman and Glomus mosseae (Nicol. & Gerd.) Gerdemann & Trappe had no effect on the shoot d. wt and P uptake when the bulk density of the soil was [ges ]1·40 and [ges ]1·60 Mg m−3, respectively. Soil compaction to a bulk density of 1·60 Mg m−3 had no effect on the percentage of root length colonized by G. intraradices and Glomus sp. City Beach, but total root length colonized decreased as soil compaction was increased. Decreased P uptake and growth of clover plants colonized by G. intraradices and Glomus sp. City Beach, with increasing soil compaction up to a bulk density of 1·60 Mg m−3, was mainly attributed to a significant reduction in total root length colonized and in the hyphal biomass. Soil compaction, which increased bulk density from 1·20 to 1·75 Mg m−3, reduced the O2 content of the soil atmosphere from 0·16 to 0·05 m3 m−3. The absence of any observable mycorrhizal growth response to any of the four species of VAM fungi in highly compacted soil (bulk density = 1·75 Mg m−3) was attributed to the significant decrease in the O2 content of the soil atmosphere, change in soil pore size distribution and, presumably, to ethylene production.

Whereas much is known of the short-term growth response to elevated atmospheric CO2 concentrations, [CO2]elev, there is relatively little information on how the response of native species is modified by temperature, despite the fact that an increase in global mean temperature is expected to accompany the rise in [CO2]. In this study, five functionally related annual native species were exposed to different combinations of ambient and elevated [CO2] and temperatures in order to assess their response in terms of growth and allometry. Fast-growing annuals were selected for the study because their growth responses could be assessed over a major portion of the plant's life cycle and in as short a period as 8 wk. Plants were grown in eight hemi-spherical glasshouses, programmed to track outside ambient conditions and provide a replicated experimental design. Treatments comprised (i) current ambient [CO2] and temperature, (ii) elevated [CO2] (ambient+34 kPa), and ambient temperature (iii) ambient [CO2] and elevated temperature (ambient+3°C) and (iv) elevated [CO2] and elevated temperature (T°Celev). All five species responded positively to [CO2]elev, although the response was statistically significant for only one, Poa annua L. Averaged over all five species, [CO2]elev increased total plant biomass by 25% (P=0·005) at 56 d, reflecting a proportionally greater increase in leaf and stem mass relative to root weight. Elevated [CO2] had no effect on leaf area, either at the individual species level or overall. Elevated T°C, by contrast, had little effect on shoot growth but increased root mass on average by 43% and leaf area by 22%. Few interactions between elevated [CO2] and T°C were observed, with the CO2 response generally greater at elevated than ambient T°C. Both [CO2]elev and T°Celev resulted in a transient increase in relative growth rate, (rgr), during the first 14 d exposure and a 3°C increase in temperature had no effect on the duration of the response. CO2 stimulation of growth operated through a sustained increase in net assimilation rate. (nar), although the potential benefit to rgr was offset by a concurrent decline in leaf area ratio (lar), as a result of a decrease in leaf area per unit leaf mass (sla). The response to T°Celev was generally opposite of that to [CO2]elev. For example, T°Celev increased lar through an increase in sla and this, rather than any effect on nar, was the major factor responsible for the stimulation of rgr. Allometric analysis of CO2 effects revealed that changes in allocation observed at individual harvests were due solely to changes associated with plant size. Elevated T°C, by contrast, had a direct effect on allocation patterns to leaves, with an increase in leaf area expansion relative to whole plant mass during the initial stages of growth and subsequent increased allocation of biomass away from leaves to other regions of the plant. No change in the allometric relation between roots and shoots were observed at either elevated [CO2] or T°C. We conclude, therefore, that allocation of biomass and morphological characteristics such as sla, are relatively insensitive to [CO2], at least when analysed at the whole-plant level, and where changes have been observed, these are the product of comparing plants of the same age but different size.

The sampler extracts uncompressed cores of 13·3 cm in diameter, up to 70 cm long, from the surface layers of peat. It has two close-fitting concentric cylindrical tubes, the outer one acting as a cutter and the inner one as a collector. As the outer tube is introduced by rotation into the peat, the cut core is collected in the inner tube which is maintained in a fixed position during the rotation phase and then pushed down stepwise. This limits friction between the peat core and the wall of the corer and prevents compression or distortion of the peat. These problems are also reduced by means of three skew cutters allowing the peat to be supported during the slicing action. Air can penetrate between the tubes to the lower end of the core, suppressing any suction effect during withdrawal. The sampler has been tested and has worked satisfactorily in many different peat types.