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28 Communication Between Undamaged Plants by Volatiles 431<br />

28.4<br />

Conclusions and Future Prospects<br />

The work reviewed here shows that chemical communication takes place<br />

between undamaged plants, supporting aspect 1 in our definition of allelobiosis<br />

(see “Introduction”). It appears that this communication affects<br />

not only the plant itself, but also organisms at higher trophic levels, namely<br />

insect herbivores and their natural enemies (aspect 3). It also raises the idea<br />

that a barley individual may benefit from the communication (aspect 2) by<br />

detecting neighbouring plants via the airborne volatiles they produce. It is<br />

most relevant to discuss this latter aspect in the context of the results on<br />

plant biomass allocation.<br />

In experiments with two barley cultivars, Ninkovic (2003) showed that<br />

when plants of a particular barley cultivar were exposed to volatiles from<br />

a different cultivar the exposed plant changed its pattern of biomass allocation,<br />

allocating more biomass to roots and less to leaves (Fig. 28.3).<br />

This pattern did not arise when plants were exposed to volatiles from the<br />

same cultivar (self-induction). This selectivity may be due to the presence<br />

or absence of specific substances in the volatile blends, but this is not necessarily<br />

the case. It is important not to overlook the possibility that the<br />

amounts of trivial plant compounds or the specific ratios between some of<br />

these might constitute the active signal. This presents a challenge to the<br />

chemical identification of the signal mechanism itself, but clearly this has<br />

high priority for study since increased knowledge in this area will lead both<br />

to greater understanding of the ecological role of allelobiosis as well as to<br />

possible applications in crop management.<br />

Even though plants of the exposed cultivar modified their pattern of<br />

biomass allocation, both the total biomass and the RGR were not significantly<br />

different from those of unexposed plants. Further, exposed plants<br />

did not undergo any alteration of physiological activity compared with<br />

unexposed plants. Here it is interesting to speculate whether, in the barley<br />

model system, volatiles from a different cultivar represent a stimulus<br />

that mobilises a morphological plasticity in the exposed cultivar that allows<br />

it to respond to potential competition from a neighbouring plant. In<br />

this scenario, allelobiosis would represent a source of information for the<br />

responding plant.<br />

Allelobiosis causes changes in exposed barley plants that make them less<br />

suitable for aphid settling than unexposed plants. From the perspective of<br />

the responding plant, allelobiosis can be viewed as a route for obtaining<br />

information on plant competitors, which should give an advantage. Alternatively,<br />

it can be considered as a chemical disturbance that is detrimental.<br />

For the herbivore, however, it should be advantageous to detect the changes<br />

in plant status associated with either situation, if these make the plant less

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