The numerous reports on declining amphibian populations throughout the world led to the creation in December 1990 of the Declining Amphibian Populations Task Force (DAPTF), activated by the Species Survival Commission of the International Union for the Conservation of Nature and Natural Resources, one of whose main goals is "the identification of target populations, species, and regions which merit immediate attention." We want to highlight one such target region, the Iberian peninsula, and a particular species, Rana perezi. Despite major efforts on behalf of the Spanish conservation authorities to preserve local and endemic species and the fact that the Iberian peninsula is considered one of the redoubts of biodiversity in Europe, locally adapted populations are menaced by the potentially fatal effects of events such as species translocations (Dodd & Seigel 1991; Reinert 1991). If a unique reproductive mode such as hybridogenesis is added to the problem of species translocation, the difficulties of preserving local species increase. Hybridogenesis is widely prevalent in European water frogs, having originated in the Rana esculenta complex, which includes seven species, and a series of hybridogenetic lineages stemming from interspecific hybridizations. Several systems, consisting of a host species (or parental species) and a hybridogenetic lineage in each, are found throughout Europe (Graf & Polls-Pelaz 1989). During gametogenesis in such systems the hybrid premeiotically excludes one of its parental genomes by producing only gametes containing the other parental genome. This remaining genome is transmitted clonally because premeiotic exclusion implies prevention of recombination through crossing over. In most cases the genome of one of the species, generally R ridibunda, is clonally transmitted, whereas the other parental genome is excluded. In general, the lost genome corresponds to that of the species living in sympatry with the hybrid. Because of its special way of reproduction, hybridogenesis may present new problems for the conservation of natural populations. The voluntary or fortuitous introduction of samples from other species of Rana capable of provoking hybridogenesis can cause alterations that can modify the genetic structure of local parental populations. The hybrids may act as transmitters of allelic variants that could profoundly modify the gene frequencies in the original populations. A highly successful hybrid is expected because survival of hybrids has been demonstrated to be superior to that of parentals in experimental nonhybridogenetic hybrid populations of other animal species (Howard et al. 1993). Hybrid individuals also tend to have other advantages, such as higher growth rates, lower metabolic demand, and resistance to diseases. In addition, their developmental periods are often faster and more stable (Mitton & Grant 1984; Mitton et al 1986; Allendorf & Leary 1986; Ledig 1986). Nevertheless, due to sterility, these hybrids would present a reduced fitness compared with hybridogenetic populations. One of these hybridogenetic systems corresponds to the hybridization between R perezi and R ridibunda, found in southern France and northeastern Spain. The distribution of hybrid populations in strictly delimited, and, in recent studies on the genetic variability of the parental syntopical species R perezi (262 individuals, 29 populations), we found significant differences in the rate of polymorphism between those populations where hybridization occurs and the remaining ones in central and western Spain where hybridogenetic hybrids were not originally found (Mann-Whitney U-test, U = 0.014, p < 0.02). During the course of our study, an introduction of the bullfrog (Rana catesbeiana) and of water frogs from northern Italy occurred in the Sierra de Gata (western Spain) from a nearby, unsuccessful frog farm (GarciaPaper submitted February 28, 1994; revised manuscript accepted June 2, 1994.