SUMMARYFollowing the uptake of tritiated thymidine during the latter part of the synthesis (S) phase of mitosis the distribution of label at metaphase varies between chromosomes and between segments within chromosomes. Per unit volume B chromosomes are more densely labelled than the normal, A chromosomes of the rye complement. Within A chromosomes the terminal segments and centromere regions are the most heavily labelled.Analyses are presented which distinguish between the different causes of heavy labelling. In terminal segments of the long arms late completion of DNA synthesis in heterochromatin contributes to the heavy labelling. In contrast the disproportionately heavy labelling in B's is attributable to a higher DNA density in B, as compared with A chromosomes, at metaphase. It is probable that the heavy labelling around the centromeres of rye chromosomes is, also, a reflection of a higher DNA density at metaphase. Our evidenceindicates it is not due to a late completion of DNA synthesis.B chromosomes have no influence upon the pattern of labelling in A chromosomes. It is possible that they reduce the rate of DNA synthesis during S.