The Fox Sparrows, Passerella iliaca, include multiple groups and subspecies distributed at several latitudes from the Alaskan arctic to the southwestern United States. As such, this species represents a potential model for investigating latitudinal variation in androgen secretion and aggressive territoriality in male passerines. Breeding male Fox Sparrows from two subspecies within two groups, the Sooty Fox Sparrow, P. i. sinuosa, and the Red Fox Sparrow, P. i. zaboria, were assessed for aggressive territoriality and androgen responsiveness at multiple latitudes in arctic and subarctic Alaska. Subarctic Sooty Fox Sparrows had higher circulating androgen levels in the early (8.54 ng/ml) versus mid–late breeding season (2.44 ng/ml). Males in the mid–late breeding season did not up-regulate androgen secretion in response to social challenge, but were aggressive and spent more time within 5 m of a decoy during a simulated territorial intrusion (STI) than early breeding males. Male subarctic Red Fox Sparrows had slightly higher circulating androgen levels (2.29 ng/ml) than arctic males (1.10 ng/ml) in the mid–late breeding season. However, androgen levels were not correlated with blood collection time after a social challenge in either group, suggesting that neither arctic nor subarctic males up-regulate androgen secretion during the mid–late breeding period. Arctic males spent more time within 5 m of a decoy and sang less than subarctic males during an STI in the mid–late breeding season. These findings demonstrate that the Fox Sparrow is a tractable model for investigating the latitudinal regulation of aggressive territoriality and androgen responsiveness in passerines.

Biological steroids were traditionally thought to be synthesized exclusively by the adrenal glands and gonads. Recent decades have seen the discovery of neurosteroid production that acts locally within the central nervous system to affect physiology and behavior. These actions include, for example, regulation of aggressive behavior, such as territoriality, and locomotor movement associated with migration. Important questions then arose as to how and why neurosteroid production evolved and why similar steroids of peripheral origin do not always fulfill these central roles? Investigations of free-living vertebrates suggest that synthesis and action of bioactive steroids within the brain may have evolved to regulate expression of specific behavior in different life history stages. Synthesis and secretion of these hormones from peripheral glands is broadcast throughout the organism via the blood stream. While widespread, general actions of steroids released into the blood might be relevant for regulation of morphological, physiological, and behavioral traits in one life history stage, such hormonal release may not be appropriate in other stages. Specific and localized production of bioactive steroids in the brain, but not released into the periphery, could be a way to avoid such conflicts. Two examples are highlighted. First, we compare the control of territorial aggression of songbirds in the breeding season under the influence of gonadal steroids with autumnal (non-breeding) territoriality regulated by sex steroid production in the brain either from circulating precursors such as dehydroepiandrosterone or local central production of sex steroids de novo from cholesterol. Second, we outline the production of 7α-hydroxypregnenolone within the brain that appears to affect locomotor behavior in several contexts. Local production of these steroids in the brain may provide specific regulation of behavioral traits throughout the year and independently of life history stage.