Several authors have proposed that speciation frequently occurs when a popu
lation becomes fixed for one or more chromosomal rearrangements that reduce
fitness when they are heterozygous. This hypothesis has little theoretical
support because mutations that cause a large reduction in fitness can be f
ixed through drift only in small, inbred populations. Moreover. the effects
of chromosomal rearrangements on fitness are unpredictable and vary signif
icantly between plants and animals. I argue that rearrangements reduce gene
flow more by suppressing recombination and extending the effects of linked
isolation genes than by reducing fitness. This unorthodox perspective has
significant implications for speciation models and for the outcomes of cont
act between neospecies and their progenitor(s).