Hirsch and his associates'--have selected positively and negatively geotactic, and positively and negatively phototactic, strains in Drosophila melanogaster. Dobzhansky and Spassky6 obtained by similar selection positively and negatively geotactic strains in Drosophila pseudoobscura, as well as positively and negatively phototactic strains in the same species (unpublished data). The selection was made with the aid of classification mazes described by the authors referred to above.1-' The wild and laboratory strains of both species of Drosophila are mostly neutral on the average with respect to geotaxis as well as to phototaxis; however, they contain both positive and negative variants that are genetically conditioned, and the heritability is high enough for selection to make fairly rapid progress.The geotactically and phototactically positive and negative strains appear to be indistinguishable in external morphology. The size, coloration, and other traits of the selected strains seem to be unchanged (no biometric study has, however, been made). Nevertheless, as the experiments described in this report show, they differ in inating preference. A slight, but statistically quite significalit, sexuial isolation has arisen as a by-product of selection for geo-and phototaxis.Material and Technique.-Geo-and photopositive and negative strains were obtained through the courtesy of Mr. Boris Spassky. They were derived from the same basic population, which was in turn obtained by hybridizing 12 strains of D. pseudoobscura homokaryotypic for AR gene arrangement and 12 strains homokaryotypic for CH gene arrangement in the third chromosome, The ancestors of these flies were collected at Pifion Flats, Mount San Jacinto, California, and the strains were kept in the laboratory for several years. The first generation in which the selection was practiced was the F2 from the crossing of AR and CH strains.The selection was made (by MIr. Spassky) as follows. In each generation, 300 virgin females and 300 males, aged separately for 3-4 days, were run, also separately, through either the geotaxis or the phototaxis maze. The 25 most positive, or the 25 most negative, individuals were selected, and allowed to reproduce in a population cage. Four lines were thus formed, selected for positive or negative geotaxis or phototaxis, respectively. Samples of the flies from these lines were obtained after Mr. Spassky had made his fifth selection. (S-5), and again after he had made his eleventh selection (S-11). The progenies of these flies, grown in ordinary half-pint culture bottles, served as material for observation of the sexual behavior.The observation chambers constructed by Ellens7' 8 were ised. Virgin females and males were aged for 5 days at 240C. Ten females and ten males of each of two strains were introduced into an observation chamber without etherization. To make the strains distinguishable, one wing was clipped in one or in the other strain; in the repeated runs the strain which had a wing clipped was alternated. The flies in the ch...
The effect of temperature and sex on spatial distribution of Drosophila melanogaster adults was studied in a specially designed apparatus. It was observed that individuals tend to aggregate in sections of the sphere independently of sex and temperature. Nevertheless, decrease in temperature increase aggregation. The mobility of both males and females indicates a negative geotactic tendency.
The choice of oviposition sites in females of Drosophila is the result of comples behavior patterns which can be modified by a number of factors. Among these, the presence of eggs or larvae induces other females to oviposit in the dame place. The relative size of the population and the coexistence with females of a diffcrcnt spccics arc some of the other environmental variables involved (DEL SOLAR and PALomxo, lDGG, 1071 ; DEL .SOLAR and GODOY, 1073). Other factors may be resolved on the a decision making D of the females : differcnt typcs of culturc mcdin or changes in the surfacc availnble for oviposition (DAVID, 1070 ; DAVID d al, 1960 ; DEL SOLAR et al., 10GG). Medium sccnted by mnlcs of the Same species (HAINARDI, 1068) or chemical stimuli in the form of solutions of acetic acid and odorous oils (CLUTTER-BUCK and BEARDMORE, 10G1), may induce attractive or rcpulsivc rcsponses of tlic flies. I n addition, VOLPE d al. (1067) and CARFAGNA el al. (1071) havc shown that the rate of egg laying in D. iiielanogaster wild type and its mutants B brown D and 4 vcrmilion o on diffcrcnt colorcd papers, seems to be relatcd to the estrarctinal pigmcnt of tlicir cyes. This paper dcscribcs the results of I I study of the pattcrns of cgg laying of D. nielanogasfer females on culture media colored with different chemical substances. 260 DAVID J. and VAN EIEnnEwEcE J., 10G9riclioii repulsive de la kvlcre vivanle sur ['miposilion de D. mclnnognstcr. R.C. Acnd. Sc. Paris. 108 : 1778-1780. DEL SOLAR E. and GODOY It., 1073-Eleccidn dcl silio de oviposici6tr en I). mclnnognstcr 9 D. funcbris. Influencia del famatio rclnlioo de la poblacidn. Rol. SOC. Uiol. Conccpcih, 46 : 127-137. DEL SOLAR E. and PALOMISO €I., l0GG-Clroice of ooiposilion in Drosopliila mclanognstcr. Ani. A'nl., 100 : 127-133. JIAIXARDI M., 1008-Gregarious oviposifion oitd plterotnones i n Drosopliila mclanognstcr. JIAIXARDI)I., l D G 0-Oviposilion pre1erenccs ~I I I). mclanognstcr and D. siinulnns. Boll. I'ALOJIINO €1. y DEL SOLAR IS., 1071-Eleccidn del silio de ociposicidn en Drosopliila. Coezisfcncia de D. mclanognstcr y D. funebris. Genet. Ibbrica, 23 : 25-33. VOLPE P., CARFAGXA 31. and DI L o n w z o JI., l0G7-Ezlrarelinal pigmenlalion and color discriininalion. I. Choice 01 color of subslrale during oviposilion i n D. mclanognstcr.
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