Conservation of germplasm from endangered and genetically valuable individuals is a high priority for all classes of animals. However, the large avian oocyte and the inability to consistently super ovulate birds make techniques such as cloning and oocyte cryopreservation unlikely tools for avian conservation. Instead, the use of domestic birds as hosts to produce sperm of exotic species for use in artificial insemination may be a practical approach to conserve avian germplasm. During early embryonic development the primordial germ stem cells (PGCs) circulate in the blood vessels prior to colonization of the gonadal ridge. These circulating PGCs are the precursors for the adult germ stem cells (GSCs), which allow continual production of sperm throughout the lifetime of males. Previous studies have demonstrated the usefulness of embryonic PGC transfers for preserving rare chicken lines, introducing transgenes, or xenotransfer between chicken, quail and turkeys. We propose that the use of non-seasonal domesticated hosts (e.g. chickens or quail) can ensure year-round production of genetically valuable sperm for use in assisted reproductive technologies such as artificial insemination. In this study adult quail testes were dispersed with collagenase prior to injection into the viteline vein of stage 15-18 chicken embryos coincident with endogenous PGC migration. Host chicken gonads were collected at day 8 of incubation and collagenase dispersed. Donor (quail) derived cells were detected by the quail specific antibody QH1 and counted by flowcytometry. Up to 2.3% of chicken embryo gonadal cells were positive for QH1 and presumably derived from the quail donor testis. This model system will be used to develop techniques for isolation and xenotransfer of GSCs collected during necropsy of adult birds, thereby enhancing the preservation of genetic material from endangered or genetically valuable specimens. (poster)