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19 Electrical Signals in Long-Distance Communication in Plants 285<br />

The coupling between APs and functioning of digestive glands remains<br />

elusive. The presence of the prey is not necessary to induce the process.<br />

It is possible to evoke an extensive release of a digestive fluid by electrical<br />

stimulation of an immobilized trap (Trebacz, unpublished).<br />

A. vesiculosa,acloserelativeofDionaea,shutsdownitstrapsafterasingle<br />

stimulation of a trigger hair followed by generation of a single AP (Iijima<br />

and Sibaoka 1982). When the trap receives only one stimulus it begins to<br />

open after 1 h. More stimuli make that the trap lobes press tightly against<br />

each other. Thus, in Aldrovanda, the system protecting against accidental<br />

stimulation is somewhat simpler than that in Dionaea. Instagnantwater,<br />

where it grows, such a sophisticated mechanism does not seem necessary.<br />

Iijima and Sibaoka (1983) pointed out that traps of Aldravanda possess<br />

a motor zone consisting of cells located in a central part of the trap between<br />

two epidermal layers. A massive efflux of ions attributed to that zone<br />

causes a loss of turgor and a sudden trap closure.<br />

The physiological significance of AP-regulated movements of leaves and<br />

pinna-rachis in other plant species, like M. pudica, Biophytum dendroides<br />

and Desmodium motorium is a matter of discussion, although the coupling<br />

between the AP and the movement is well documented (Sibaoka 1973;<br />

Antkowiak and Engelmann 1995).<br />

In Mimosa, itwasshownthatnotonlythemovementbutalsoaphotoassimilate<br />

unloading from the phloem occurs following an AP (Fromm<br />

and Eschrich 1988). A similar effect was demonstrated in Zea mays,which<br />

makes it probable that it is common in excitable plants.<br />

APs also play a role in plant pollination and fertilization. The most<br />

spectacular example was described by Sinyukhin and Britikov (1967) in<br />

Incarvillea. Its flowers possess a bilobal stigma which closes upon mechanical<br />

stimulation exerted by a falling pollen grain. The movement which is<br />

mediatedbytheAPleadstopollengrainarrestinsidethestigma.Soon<br />

afterthat,thesecondAPtravelstotheovary,whereitevokesasignificant<br />

increase in respiration long before fertilization. APs evoked by pollination<br />

were also found in Lilium and Hibiscus (Fromm et al. 1995). The large dimensions<br />

of the pistils, which made electrode attachment easy, determined<br />

the selection of these objects. It is possible that the phenomenon is more<br />

general in flowering plants. APs were registered during movement of stamens<br />

in Berberis and Mahonia too (Simons 1981). APs were postulated to<br />

mediate between illumination and guttation in gametophytes of the moss<br />

Bryum pseudotriquetrum (Sinyukhin 1973). Drops of liquid appearing by<br />

guttation enable fertilization.<br />

Excitation also influences gas exchange in plants. The significant increase<br />

of respiration following stimulation of the C. conicum thallus is<br />

well documented (Dziubinska et al. 1989). It was demonstrated that both<br />

damaging (cutting of a thallus edge) and nondamaging electrical stimuli

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