The hybrids obtained after crossing N. Tabacum (n = 24) X N. sylvestris (n = I2), N. Tabacum (n = 24) X N. Rusbyi (n = I2), N. sylvestris (n = 12) X N. Rusbyi (n = I2), and from the reciprocal crosses are self-sterile under normal conditions. The cytological studies on these three species hybrids (Kostoff, I930) showed that in the pollen mother cells (PMC's) of the first two there were 12 bivalent and 12 univalent chromosomes appearing during the first meiotic division, while in the hybrid of the third cross, N. sylvestris X N. Rusbyi, 24 univalent chromosomes were usually found. The latter cross combination formed occasional dyads with 2n, i.e. 24, chromosomes instead of tetrads as a result of omission of the first meiotic division. This occurred most frequently when the hybrid plants from this cross grew under conditions of insufficient water supply and intense sunshine. When N. Tabacum was pollinated with pollen from the hybrid N. sylvestris X N. Rusbyi containing a relatively high percentage of pollen grains originating from such dyads, seeds were obtained from which very vigorous plants-triple hybrids, N. Tabacum X (N. sylvestris X N. Rusbyi)-were raised (P1. X, figs. I and 2). Among these triple hybrid plants intermediate types were found as well as those that resembled more closely one of the parental plants in respect to certain characters. The intermediate types (figs. I, 2, and 3) proved to be fully fertile while the others were only partially so. Cytological studies on both types of plants were made and it was found that the partially fertile plants had a relatively irregular reduction division and usually 48 + i, or 48 + 2 somatic chromosomes, while the fertile intermediate triple hybrids had normal, regular, reduction division (figs. 4 and 5), and had 24 chromosomes in the PMC's (fig. 4) and 48 in the root tips (figs. 6 and 7). The origin of these fully fertile triple hybrids can be explained on a cytological basis as follows: As manifested by the F1, half of the chromosomes of N. Tabacum (n = 24) have an affinity for the chromosomes of N. sylvestris (n = 12) and the other half (I2) have an affinity for those of N. Rusbyi, while the chromosomes of N. sylvestris do not manifest any such affinity for the chromosomes of N. Rusbyi as also observed in the F1 plants. However, after pollinating N. Tabacum with pollen from F1 (N. sylvestris X N. Rusbyi) which contained a high percentage of abortive grains and also those originating from dyads with 24 chromosomes (12 from N. sylvestris and I2 from N. Rusbyi conse-