We propose to give in a series of papers an account of the mutant races of Drosophila and the linkage shown in their inheritance. In this paper we shall consider only the members of the first chromosome, describing a large number of new mutants with their linkage relations and summarizing to date all the linkage data relating to the first chromosome. In later papers we propose to consider the members of the second, third, and fourth chromosomes.
The list at the top of page 21 gives the names of the factors dealt with in this paper. They stand in the order of their discovery, the mutant forms reported here for the first time being starred.
In each experiment the percentage of crossing-over is found by dividing the number of the cross-overs by the sum of the non-cross-overs and the cross-overs, and multiplying this quotient by 100. The resulting percentages, or cross-over values, are used as measures of the distances between loci. Thus if the experiments give a cross-over value of 5 per cent for white and bifid, we say that white and bifid lie 5 units apart in the X chromosome. Other experiments show that yellow and white are about 1 unit apart, and that yellow and bifid are about 6 units apart. We can therefore construct a diagram with yellow as
the zero, with white at 1, and with bifid at 6. If we know the cross-over values given by a new mutant with any two mutants of the same chromosome whose positions are already determined, then we can locate the new factor with accuracy, and be able to predict the cross-over value which the new factor will give with any other factor whose position is plotted.
The sex-linked factors of Drosophila.
| Gen. | Part affected. | Figure. | Symbol. | Locus. | Date found. | Found by. | |
| White | Eye-color | 11 | w | 1.1 | May | 1910 | Morgan. |
| Rudimentary | Wings | A | r | 55.1 | June | 1910 | Morgan. |
| Miniature | Wings | 7-8 | m | 36.1 | Aug. | 1910 | Morgan. |
| Vermilion | Eye-color | 10 | v | 33.0 | Nov. | 1910 | Morgan. |
| Yellow | Body-color | 5 | y | 0.0 | Jan. | 1911 | Wallace. |
| Abnormal | Abdomen | 4 | A′ | 2.4 | July | 1911 | Morgan. |
| Eosin | Eye-color | 7-8 | we | 1.1 | Aug. | 1911 | Morgan. |
| Bifid | Wings | B | bi | 6.3 | Nov. | 1911 | Morgan. |
| Reduplicated | Legs | 34.7 | Nov. | 1911 | Hoge. | ||
| Lethal 1 | Life | l1 | 0.7 | Feb. | 1912 | Rawls. | |
| Lethal 1a* | Life | l1a | 3.3 | Mar. | 1912 | Rawls. | |
| Spot* | Body-color | 14-17 | ys | 0.0 | April | 1912 | Cattell. |
| Sable* | Body-color | 2 | s | 43.0 | July | 1912 | Bridges. |
| Dot* | Thorax | 33 ± | July | 1912 | Bridges. | ||
| Bow* | Wings | C | Aug. | 1912 | Bridges. | ||
| Lemon* | Body-color | 3 | lm | 17.5 | Aug. | 1912 | Wallace. |
| Lethal 2 | Life | l2 | 12.5± | Sept. | 1912 | Morgan. | |
| Cherry | Eye-color | 9 | wc | 1.1 | Oct. | 1912 | Safir. |
| Fused* | Venation | D | fu | 59.5 | Nov. | 1912 | Bridges. |
| Forked* | Bristles | E | f | 56.5 | Nov. | 1912 | Bridges. |
| Shifted* | Venation | F | sh | 17.8 | Jan. | 1913 | Bridges. |
| Lethal sa | Life | lsa | 23.7 | Jan. | 1913 | Stark. | |
| Bar | Eye-shape | 12-13 | B′ | 57.0 | Feb. | 1913 | Tice. |
| Notch | Wing | N′ | 2.6 | Mar. | 1913 | Dexter. | |
| Depressed* | Wing | G | dp | 18.0 | April | 1913 | Bridges. |
| Lethal sb | Life | lsb | 16.7 | April | 1913 | Stark. | |
| Club* | Wings | H | cl | 14.6 | May | 1913 | Morgan. |
| Green* | Body-color | May | 1913 | Bridges. | |||
| Chrome* | Body-color | Sept. | 1913 | Bridges. | |||
| Lethal 3 | Life | l3 | 26.5 | Dec. | 1913 | Morgan. | |
| Lethal 3a | Life | l3a | 19.5 | Jan. | 1914 | Morgan. | |
| Lethal 1b* | Life | l1b | 1.1- | Feb. | 1914 | Morgan. | |
| Facet* | Eye | fa | 2.2 | Feb. | 1914 | Bridges. | |
| Lethal sc | Life | lsc | 66.2 | April | 1914 | Stark. | |
| Lethal sd | Life | lsd | May | 1914 | Stark. | ||
| Furrowed | Eye | fw | 38.0 | Nov. | 1914 | Duncan. | |
The factors are located preferably by short distances (i.e., by those cases in which the amount of crossing-over is small), because when the amount of crossing-over is large a correction must be made for double crossing-over, and the correction can be best found through breaking up the long distances into short ones, by using intermediate points.
Conversely, when a long distance is indicated on the chromosome diagram, the actual cross-over value found by experiment (i.e., the percentage of cross-overs) will be less than the diagram indicates, because the diagram has been corrected for double crossing-over.