PREFACE The last exhaustive compilation of genetic variations of Drosophila melanogaster was "The Mutants of Drosohpila melanogaster" prepared by Calvin B. Bridges and Katherine S. Brehme; it was published in 1944 and was complete through 1942. This volume is a revision of their work; it contains new information on variants already described and descriptions of variants discovered since 1942; it is reasonably complete through 1966. The new material was extracted from the literature, from Drosophila Information Service, and from voluminous contributions of unpublished material supplied by Drosophila geneticists throughout the world. The revision describes genetic material currently available to Drosophila geneticists and extinct material that may be encountered in earlier literature on the subject. The work of Bridges and Brehme was divided into two sections, one describing wild-type stocks and the other describing the known departures from the normal genotype. Our revision is divided into seven sections: (1) mutants, with about 3000 entries; (2) chromosome aberrations, more than 1500 entries; (3) special chromosomes, i.e., multiply marked chromosomes, balancers, compound chromosomes, Y derivatives, and X-Y combinations; (4) cytological markers; (5) departures from diploidy; (6) nonchromosomal inheritance; and (7) wild-type stocks. All except the first two groups have relatively few entries. Several new categories of effects unknown or nearly so in 1942 are included here. (1) Pseudoalleles: the intensive investigations into pseudoallelism and complementation dating from the pioneering work of E. B. Lewis on Star and astroid (1945, Genetics 30: 137-66) have produced information on the genetic fine structure of many loci. (2) Isozymes: a series of genetically controlled enzyme polymorphisms and deficiencies described mostly in the last decade; their discovery was made possible by the development of gel electrophoresis. (3) Compound chromosomes: formed by the attachment of two doses of one chromosome arm to a single centromere; represented by only the attached-X chromosome in the original edition, the various classes of compound chromosomes now available occupy an entire subsection. (4) Marked Y chromosomes: Y chromosomes marked by the genes carried on small attached euchromatic segments derived from the X or an autosome. (5) Reciprocal translocations between the X and Y chromosomes. (6) Attached XY chromosomes: chromosomes with the portions of the X and Y chromosomes necessary for male viability and fertility attached to a single centromere. Development of the system of nomenclature designating genetic variations of Drosophila melanogaster has been rather haphazard; consequently, the system is not a logical structure but is replete with relics, redundancies, and inconsistencies. Revision into a consistant scheme is not practicable, creating as it would a chaotic discontinuity in the literature. Even were such a revamping considered desirable, design of such a system is not obvious, since a change proposed to obviate one inconsistency would likely create more conflicts than it alleviated. Therefore, with few exceptions, we have adhered to the conventions established by Bridges and Brehme in the original volume. Some changes were made to correct glaring inconsistencies and others to facilitate automatic handling of Drosophila symbols. July 1967 The conventions adopted for naming and symbolizing different types of genetic changes are discussed at the beginning of the different sections of the book. Symbols of all genetic variants both normal and abnormal are always italicized but their names in text are printed in roman. We are grateful to our colleagues throughout the world for their cooperation in making available to us their unpublished observations and in responding to our numerous queries. Special thanks are due Doctors E. G. Lewis, the late H. J. Muller, J. Schultz, and A. H. Sturtevant, who served as an informal board of consultants. They have contributed a measure of success to this effort but bear no responsibility for its shortcomings.