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48 P.W. Barlow<br />

reception of his book The origin of species, he might well have kept any<br />

ideas about plants possessing brains strictly to himself.<br />

One attribute of a brain, as the term is commonly understood, is that<br />

it is an organ with a definite structure and location which gathers or<br />

collects information, which was originally in the form of vibrations (heat,<br />

light, sound, chemical, mechanical, . . .) in the ambient environment and<br />

somehow transforms them into an output or response. Interestingly, the<br />

execution of these responses is by means of another vibrating system –<br />

the circumnutating root (Darwin 1880). Any change in the direction of<br />

thestimulustemporarilyoverridesthenutationalprocessuntiltheusual<br />

orientation of the plant organ is regained. Maybe this was how Darwin<br />

understood the situation. However, the absence of obvious nervous tissue<br />

wouldhavebeenaseriousprobleminhisfurtherpursuitofthematter.But<br />

the situation has changed in recent years, as other chapters in this book<br />

will show. With the discovery within plants of many of the components<br />

of animal-type nervous systems (Baluška et al. 2004), the question is how<br />

this new knowledge can be conceptualised, and whether any paradigm<br />

will emerge which acknowledges some sort of plant nervous system; and<br />

moreover, whether this nervous system will have features which can be<br />

generalised to all eukaryotic organisms.<br />

In recognising the possession, by the root apex, of a brain-like function,<br />

alacunaisfilledinapplyingMiller’scomprehensivelivingsystemstheory<br />

to plants. Consequently, there is now scope for analysing the informationprocessing<br />

subsystems and linking them with the other two major types<br />

of subsystems that process matter and energy (Barlow 1999). This task can<br />

be done at the various levels of organisation that characterise all biological<br />

constructions.<br />

The subsystems are not static artefacts of theory, but represent inherently<br />

dynamic processes by which biological constructions act. They apply not<br />

only to large constructions such as social communities, but also to smaller<br />

microcosms such as cells. Indeed, the subsystems fulfil the role of the ‘coordinative<br />

conditions’ which the physicist and systems analyst Lancelot Law<br />

Whyte had seen as providing a key to understanding biology in general:<br />

“Until the coordinating conditions have been identified no theory of phylogenesis,<br />

of ontogenesis, or of their relations, can be regarded as definitive.<br />

Moreover [they] hold the clue to the relation of physical laws and to the<br />

unity of the organism” (Whyte 1965, p. 67). For Whyte, these conditions<br />

express “the biological spatio-temporal coordination, the rules of ordering<br />

which must be satisfied . . . by the internal parts and processes of any<br />

organism capable of developing and surviving in some environment. The<br />

coordinating conditions are the expression of geometrical, 3D, or perhaps<br />

kinematic rules determining the necessary 3D or spatio-temporal network<br />

of the atoms, ions, molecules, organelles, etc. in a viable organism. They . . .

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