MONOGAMOUS social organization is characterized by selective affiliati
on with a partner, high levels of paternal behaviour and, in many spec
ies, intense aggression towards strangers for defence of territory, ne
st and mate1,2. Although much has been written about the evolutionary
causes of monogamy, little is known about the proximate mechanisms for
pair bonding in monogamous mammals2,3. The prairie vole, Microtus och
rogaster, is a monogamous, biparental rodent which exhibits long-term
pair bonds characterized by selective affiliation (partner preference)
and aggression4,5. Here we describe the rapid development of both sel
ective aggression and partner preferences following mating in the male
of this species. We hypothesized that either arginine-vasopressin (AV
P) or oxytocin (OT), two nine-amino-acid neuropeptides with diverse fo
rebrain projections, could mediate the development of selective aggres
sion and affiliation. This hypothesis was based on the following obser
vations: (1) monogamous and polygamous voles differ specifically in th
e distribution of forebrain AVP and OT receptors6,7; (2) AVP innervati
on in the prairie vole brain is sexually dimorphic and important for p
aternal behaviour8; (3) central AVP pathways have been previously impl
icated in territorial displays and social memory9,10; and (4) central
OT pathways have been previously implicated in affiliative behaviours1
1. We now demonstrate that central AVP is both necessary and sufficien
t for selective aggression and partner preference formation, two criti
cal features of pair bonding in the monogamous prairie vole.