The timing mechanisms of testicular regression and photorefgractoriness were investigated with the Houswe Finch. Testicular regression is completed by August and is followed by a month and a half photorefractory period. Resumption of complete photosensitivity is an indicidual, gradual precess of several months. Stainable neurosecretion in the median eminence of the hypothalamus appears unrelated to photorefractoriness. Lipids concentrate in regressing testes, disappear by mid—September and then the interstitium stains for fats. Changes in gametogenesis do not occur during photorefractoriness. Testicular regression can be induced at will, and photofractoriness is not a necessary concomitant thereof. Regression of intermediate sixed testes appears related to a lack of gonadotropic hormone release; growth of intermediate sized testes is probably additive on a daily basis. Regression of fully developed testes can occur spontaneously; then regression is followed by photorefractoriness Spontaneous regression can occur under continuous illumination and LD 18:6 regiments; photorefractoriness is porlonged by these regimens. testosterone injections do not induce regression, but enhance testiculargrowth. Prolactin does not affect either growth or regression of the testes, but causes bodily fattening. PMS and testosterone do not hasten refractory termination. Although both promote precocious growth, the testes regress upon hormone withdrawal. Short days (LD 6:18) and long days (LD 10:14, LD 12:12, LD 14:10) all terminate photorefractoriness equally. A circadian rhythm may contribute to termination of photorefgractoriness. Previous photorefractory control hypothesis are enumerated, types of possible timing machanisms are considered, and a new hypothesis proposed, tested, and discussed. A model of breeding control for the entire annual cycle is developed, consistent with all field and laboratory observations.