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A Critique of Pure (Genetic) Information

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A <strong>Critique</strong> <strong>of</strong> <strong>Pure</strong> (<strong>Genetic</strong>) <strong>Information</strong> 115<br />

as it does upon genetic sequence stability. Perhaps even more to the point,<br />

the very idea <strong>of</strong> order from crystalline stability must be reworked into<br />

an idea <strong>of</strong> order from dynamic steady-state systems within which crystalline<br />

structures function as constituent resources that are subject to<br />

dynamic modifications, rearrangements, expansions, contractions, and<br />

replications. Fifty years <strong>of</strong> hindsight reveals that life is indeed an orderfrom-order<br />

phenomenon but rejects the claim that the chemistry <strong>of</strong> the<br />

solid state provides the only, or even a privileged, basis for this order.<br />

With the rejection <strong>of</strong> the warrant for any claims for the primacy <strong>of</strong> a<br />

hereditary code-script, the door opens for a new overarching perspective<br />

on the nature <strong>of</strong> the living organism. And just such a perspective is beginning<br />

to emerge.<br />

Drawing on a number <strong>of</strong> disciplines and contributions [including an<br />

earlier expression <strong>of</strong> this work (Moss 1992)], new advocates <strong>of</strong> a developmental<br />

systems theory (DST) are beginning to explore the implications<br />

<strong>of</strong> a biology which is neither explicitly nor implicitly encased in the<br />

metaphorical space <strong>of</strong> the code-script.<br />

From a DST perspective, ontogeny is best viewed as contingent cycles <strong>of</strong> interaction<br />

amongst a heterogeneous set <strong>of</strong> developmental resources, no one <strong>of</strong> which<br />

‘controls’ or ‘programs’ the process. These resources range from DNA to cellular<br />

and organismic structure and to social and ecological interactions. Many <strong>of</strong><br />

these resources, both inside and outside the organism, can be reliably reconstructed<br />

down evolutionary lineages. Evolution is change in these developmental<br />

cycles. The change in gene frequency <strong>of</strong>ten used to define evolution are but<br />

one aspect <strong>of</strong> the richer complex <strong>of</strong> stabilities and changes captured by the developmental<br />

systems approach. (Oyama, Griffiths & Gray 5 2001)<br />

From the DST perspective (Oyama 1985, Griffiths & Gray 1994,<br />

Griffiths & Gray 2001) the achievement <strong>of</strong> any phenotype will rely on<br />

the presence <strong>of</strong> some set <strong>of</strong> heterogeneous resources, none <strong>of</strong> which singly<br />

determines it and the absence <strong>of</strong> any <strong>of</strong> which—be it a vitamin, a gene,<br />

or some other developmental cue—may equally result in a characteristic<br />

aberration. The developmental systems perspective is thus permissive <strong>of</strong><br />

many different kinds <strong>of</strong> biological explanations which may be tailored<br />

to local needs and local contexts. At minimum it provides a perspectival<br />

antidote to that malady by which the richness and vitality <strong>of</strong> life<br />

processes are lost by slippage into that which is (genetically) known in<br />

advance. If no developmental resource is necessarily accorded causal

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