Theories about the evolution of migratory behaviour in birds have recently
been grouped in eight categories (Rappole 1995). Common to all of them is t
he idea that migration originated in ancestral sedentary populations by som
e kind of 'behavioural jump'. These are difficult to explain, especially un
der the assumption that migration has evolved several or many times indepen
dently. Recent experimental studies undertaken to illuminate the genetics o
f bird migration and the potential and speed of the associated microevoluti
onary processes have led to another view - a simple yet comprehensive theor
y. Its central concept is (obligate) partial migration, which is extremely
widespread at higher latitudes, possibly also in the tropics, and seems to
have evolved very early or might even have been inherited from pre-avian an
cestors. Partial migration provides a behavioural turntable from which excl
usive migratoriness and sedentariness can easily and rapidly be reached (or
left) through selection and related microevolutionary processes. The fact
that all important migratory features are directly genetically controlled,
that migratoriness and amount of migratory activity are based on a common g
enetic mechanism, and that migratory syndromes exist, probably all greatly
facilitate microevolutionary changes from migratoriness to sedentariness an
d vice versa.