The production of stable phenotypes depends from the earliest stages o
f development upon high levels of somatic cellular selection amongst c
ells or cell lineages. The signals exchanged amongst cells can reveal
important aspects of a cell's phenotype, and might thereby be used in
darwinian processes of developmental selection. Based upon an optimali
ty model, we suggest that stable phenotypes require a substantial inve
stment in two mechanisms of inter-cellular selection: ''quality-select
ion'' mechanisms regulate the average phenotype of a group of cells; '
'stability-selection'' mechanisms regulate the variance in cell phenot
ypes. Variance in cell phenotypes may arise from developmental-error o
r other stochastic processes, or be generated as is true of the immune
system, as part of a developmental strategy. The model shows that sta
bility-selection mechanisms may exert the stronger effect on overall o
rgan or body performance. Selection based upon reliable inter-cellular
signalling of phenotypic properties may be the key way that bodies an
ticipate and then constrain variance in cell phenotypes around the opt
imal cellular attributes, and suggests an advantage of developmentally
-selected systems over instructional ones. High levels of investment i
n stability mechanisms also ensure homogeneous collections of cells th
at can translate ''upwards'' into developmentally stable organ systems
and phenotypes. Environmental and genetic factors, as well as the pre
valent mode of selection, may all affect developmental stability and t
hereby give rise to varying degrees of somatic selection. (C) 1998 Aca
demic Press.