Primary oocytes exist in large numbers in the ovarian cortex of young animals. They themselves seem incapable of division and their abundance is owing to the earlier multiplication of the oogonia from which they have differentiated. As a feature of differentiation, the oocyte nucleus starts upon the early prophase changes of the first meiotic division, the chromosomes become somewhat condensed, and the nucleus then passes into the dictyate stage. Those oocytes that are not destined, as many are, for early degeneration remain in this stage until meiosis is suddenly resumed shortly before or soon after ovulation. The precise form assumed by the chromosomes in the dictyate stage is uncertain though they clearly lose their earlier partially condensed appearance. In oocyte nuclei in fish, amphibians, reptiles and birds, the chromosomes take on the form of fine long threads bearing numerous lateral loops, and are referred to as lampbrush chromosomes. Their special significance is still conjectural-they may play a part in yolk synthesis. Equivalent structures have yet to be demonstrated in mammalian oocytes. Recent observations of Ohno, Kaplan and Kinosita (i960) showed that the two X chromosomes in rat oocytes are isopycnotic, both at the first meiotic prophase and the second meiotic metaphase. This is in contrast to the positively heteropycnotic state of the XY bivalent in spermatocytes, as previously demonstrated by these workers (Ohno, Kaplan and Kinosita, 1957, 1958), and they suggest that the condition in spermatocytes represents an evolved mechanism that prevents crossing-over and ensures isolation of the femaledetermining chromosome from the male-determining chromosome. Crossing-over between the two X chromosomes in oocytes, on the