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The hypothesis was to test whether a ratio of estrogen:androgen in eagle feces would reflect gonadal activity, and whether our procedure for noninvasive hormone analysis of fecal steroids could be applied to assess seasonal reproductive function in four captive bald eagles (Haliaeetus leucocephalus). Total immunoreactive excretory estrogens (E) and testosterone (T) were analyzed and compared as an E/T ratio from ad libitum monthly stool collections during the 1980-81 breeding season of birds maintained in an artificial insemination (AI) project. Since active male gonads are known to secrete a preponderance of androgens into the peripheral circulation and that renal clearance filters steroid metabolites into the urine, it was reasonable to assume that a lowered excretory E/T profile would mimic major changes in male seasonal steroidogenesis; analogously, active female gonads would result in an increased excretion of urinary estrogens, in turn reflected by a seasonal elevation of E/T ratios. A serial profile of excretory E/T ratio data for two male bald eagles approximated unity values except for a midseason low (X < 0.4) in February, one month prior to semen collections, followed by a significant end-of-breeding season rise in E/T values (X > 2.5, P < 0.01). The average E/T profile from data of two female eagles were two-to sixfold higher than males except for a significant mid-breeding season peak in E/T values during March (X > 13.5, P < 0.01). Despite the absence of nest building or egg production by either female, these preliminary observational data indicated seasonal patterns of gonadal activity in both female eagles that were synchronous with semen availability from adjacent males.

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Female green iguanas, Iguana iguana, were caught in Belize, Central America (17 degrees N), in December, at the onset of seasonal gonadal activity. The animals were immediately transferred to San Diego (32 degrees N). Ovarian follicular development continued, with peak plasma hormone levels measured in January and February; 200 pg/ml for progesterone (P) and 800 pg/ml for total estrogens (Et = estradiol [E2] + estrone [E1]). E2 was the predominant estrogen throughout the cycle. Follicular atrophy was indicated in April with circulating progesterone and estrogen levels decreasing to baseline (refractory phase) levels (P = 20 pg/ml; Et = 50 pg/ml). Approximately midway through the refractory phase of their annual reproductive cycle (late May), either the D-Arg6 analog of Chicken II or mammalian GnRH was administered via intraperitoneal osmotic pumps for 14 days to nine females. The analog of chicken II induced a fivefold increase in total circulating estrogens within 3-4 days after implantation. Both continuous and pulsatile delivery of the chicken II analog produced a similar pattern of steroidogenic response. A radical sham control animal showed no increase in steroidogenesis. Mammalian GnRH produced a pattern of similar duration, although the magnitude of the steroidogenic response was only half that produced by the chicken II analog. Estrogen titers approached baseline levels in all treatment groups two days after treatment ceased. Progesterone levels increased in all treatment groups during the delivery of exogenous GnRH, although the increases were not consistent. Untreated male cagemates housed with treated females exhibited increased territoriality, courtship behavior, and mating, which began on day 4 or 5 of the treatment period. The control female was not courted by its male cagemate.