Abstract.Vaginal cytology and vulva size were used to characterize the reproductive cycle of female blackfooted ferrets (Mustela nigripes), Siberian polecats (M. eversmanni), and domestic ferrets (M. putorius furo). Emphasis was on black-footed ferrets because of the need to breed these critically endangered animals and on Siberian polecats because of the close taxonomic relationship to black-footed ferrets. Vaginal cytology of the 3 species of ferret is similar. Proestrus was characterized by an increasing percentage of superficial epithelial cells and enlargement of the vulva. During estrus, superficial cells were usually ≥ 90% of epithelial cells in the vaginal lavage and after several days were fully keratinized. Neutrophils were more common during all stages of the estrous cycle in domestic ferrets than they were in the other species. Following copulation, percentage of superficial calls in the vagina declined and vulva swelling subsided. Large cells, probably of uterine symplasma origin, were observed in vaginal lavages following whelping or pseudopregnancy. Vaginal cytology is extremely useful in the reproductive management of black-footed ferrets and Siberian polecats. Knowledge of normal vaginal cytology could be applied to the diagnosis of female reproductive abnormalities in all 3 species.

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A captive breeding program is being conducted with black-footed ferrets (Mustela nigripes), an endangered species. Results of 5 years of study are reported. Simple, but specialized, nontraumatic handling techniques allowed assessment of reproductive status with minimal stress, which was important in breeding management. Black-footed ferrets are sexually mature and may successfully reproduce in their 1st year. Proestrus lasts approximately 2-3 weeks. Duration of estrus in unbred females was 32-42 days; females usually bred within 20 days. Most breeding activity occurred during April. Mean gestation length was 42.7 days ( 2 0 . 7 , range 42-45 days), litter size averaged 3.0 kits (51.4, range 1-6 kits), and weaned kitdlitter averaged 2.4 ( * 1.7, range 1-6 kits). Weaning rate of kits was 80%. Sex ratio of kits was essentially 1:l. Productivity was greatest among females 5 3 years of age. Rapid expansion of the captive population is possible and will be important for genetic management of the species and for achieving the primary goal of the recovery program, which is to return black-footed ferrets to the wild.

Sperm were obtained via electroejaculation from Domestic ferret, (Mustela putorius furo), Siberian ferret (M. eversmanni), Black-footed ferret (M. nigripes), and a hybrid between Siberian and Domestic, called the Fitch ferret (M. sp.). Comparisons of sperm were made by four different microscopy techniques to determine whether differences exist among species. First, Nomarski differential interference microscopy could be used to distinguish domestic ferret sperm from the others on the basis of the structure of the posterior part of the acrosome. Second, both silver staining, which demonstrates argentophilic protein distribution, and scanning electron microscopy (SEM), revealed differences among the morphology of sperm for each species; variation in the unique appearance of the acrosome in ferret sperm was detected especially well by SEM. To quantify differences in morphology, five sperm head parameters were measured using image analysis; light microscopy produced significantly larger values than did SEM (all parameters and all species but Fitch), and there were significant differences owing to species for all parameters but one. Generally, our data demonstrate the value of complementary techniques to distinguish among sperm of closely related species and more specifically may help establish evolutionary relationships among the ferret species studied. In addition, they provide baseline data important for the captive breeding of the endangered Black-footed ferret.