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426 V.Ninkovic,R.Glinwood,J.Pettersson<br />

Fig.28.3. Change in pattern of biomass allocation in barley after exposure of a plant of one<br />

cultivar to volatiles from a plant of a different cultivar. The exposed plant allocated greater<br />

biomass to roots compared with the unexposed plant, but total biomass was unchanged<br />

Even though plants exposed to volatiles from a different cultivar allocated<br />

more biomass to roots than to shoots and leaves, their relative growth<br />

rate (RGR, increase in biomass per unit biomass per unit time) and unit<br />

leaf rate (ULR, increase in biomass per unit time and leaf area, a physiological<br />

component of the RGR) were not significantly different from that<br />

of either type of control plant. However, specific leaf area (SLA, leaf area<br />

per leaf dry weight), one of the two morphological components of RGR,<br />

was significantly increased in plants exposed to volatiles from the other<br />

cultivar.Thisisinlinewithpreviousstudiesshowingthatreducedbiomass<br />

allocation to leaves can be compensated for by higher SLA (Aerst et al.<br />

1991). It has been speculated that fast-growing plants benefit from a high<br />

SLA only if leaves increase their photosynthetic activity to the maximum<br />

(Van der Werf 1996).<br />

Gersani et al. (2001) showed that individual plants sharing rhizosphere<br />

space with another plant produce more root mass than when one plant<br />

‘owns’ that space. However, it seems that root growth can be stimulated<br />

merely by volatiles from a neighbouring plant, even though the plants do<br />

not share rhizosphere space (Ninkovic 2003). This indicates that allelobiotic<br />

responses affect the whole plant, not only specific parts such as roots or<br />

leaves.

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