relationships and origins remain unresolved. For example, it is unclear
whether xenobiosis or temporary social parasitism ever lead to
inquilinism.
Social parasitism in ants and other social insects appears to be largely
a temperate-zone phenomenon and to be concentrated in particular
phylogenetic lines. Various authors have discussed factors that might be
responsible for these patterns (see Alloway, 1980, 1997; Allowayet al.,
1982; Stuart and Alloway, 1982, 1983; Buschinger, 1986, 1990; Hölldobler
and Wilson, 1990; Stuart, 1990, 1993; Topoff, 1997; and references
therein). Because most known socially parasitic social insects occur in the
temperate regions around the world, it has been suggested that cooler
temperatures might facilitate the acceptance of alien individuals into
colonies. As already discussed, the adoption of young mated queens back
into their parental nests (i.e. secondary polygyny) would seem to be
an important precursor to parasitic colony foundation. It has also been
suggested that the occurrence of closely related sympatric species in large
dense populations, which, to some extent, compete with each other,
would promote the kinds of interactions necessary for the evolution
of social parasitism; and these factors also tend to be characteristic of
temperate regions. The tendency of colonies to fragment into small, often
queenless, nest units, a trait often associated with secondary polygyny
Social Parasitism in Ants 329
Territorial
aggression
Secondary
polygyny
Intraspecific
slavery
Interspecific
slavery
Temporary
social
parasitism
Inquilinism
Xenobiosis
Plesiobiosis
Fig. 15.1. Possible evolutionary pathways for social parasitism in ants (redrawn
with modifications from Hölldobler and Wilson, 1990).