A life cycle alternating between a microscopic larva (mm-sized) and ma
croscopic adult (cm-sized) occurs commonly among invertebrates. The pa
ttern of occurrence of such a biphasic life cycle among lower metazoan
s like the Porifera and Cnidaria, as well as ultrastructure of larva a
nd adults of many invertebrates, suggests that the earliest phases of
metazoan evolution also had such a cycle. Only the dispersive larvae i
n the original metazoans could be characterized as ''small and mobile'
' if we follow this model to its logical conclusion; the adults, by co
ntrast, evolved into larger-bodied organisms to maximize reproduction
and were non-motile filter feeders for the most part. The biphasic lif
e cycle arose early in evolution, then, shortly after the first multic
ellular organisms evolved as clones of flagellated cells linked togeth
er by interactions through ECM; selective pressures acting independent
ly on the two phases of the Life cycle led to the origin of the differ
ent metazoan tissue types-epithelial, connective, nervous, and muscle
tissues. For the Bilateria, this suggests that extant acoelomate and p
seudocoelomate forms evolved through progenesis of larvae and juvenile
s in a manner like that known for the radiation of the interstitial an
nelids. A better understanding of larval biology and of mechanisms for
heterochrony is crucial for hypotheses of metazoan evolution.