Two meiotic genes from natural populations are described. A female mei
otic mutation, mei(1)g13, mapped to 17.4 on the X chromosome, causes n
ondisjunction of all homologs except for the fourth chromosomes. In ad
dition, it reduces recombination by 10% in the homozygotes and causes
18% increased recombination in the heterozygotes. A male meiotic mutat
ion, mei-1223m144, is located on the third chromosome. Although this m
utation causes nondisjunction of all chromosomes, each chromosome pair
exhibits a different nondisjunction frequency. Large variations in th
e sizes of the premature sperm heads observed in the homozygotes may r
eflect irregular meiotic pairing and the subsequent abnormal segregati
on, resulting in aneuploid chromosome complements.