“…Assuming that positrons retain their longitudinal polarization while slowing down to form Ps and looking for possible stereoselective effects, Garay et al (1973;1974a, b) studied the annihilation of positrons by the D-and L-isomers of tryptophan, phenytalanine, tyrosine and dihydroxyphenylalanine. These arguments were bolstered by the inability of several other investigators (Dezsi et al, 1974;Brandt and Chiba, 1976;Ache, 1977, 1979) who, again using ZZNa positron sources, were unable to find any significant differences whatsoever in the lifetimes or intensities of short-or long-lived components of the positron lifetime spectra observed between D-and L-enantiomers of a variety of organic compounds. Garay's results were immediately questioned by Rich (1976), who argued that the chirality of the positron would be lost during deceleration before Ps formation could occur, and that the reported results, if valid, must have another explanation.…”