CHAPTER VI.

BOOTING.

The method of inheritance of the feathering on the feet of some poultry has already been made the subject of much study. Hurst (1905, p. 152) crossed booted and non-booted birds and bred the hybrids together. He concluded that "the Mendelian principles are at work in these aberrant phenomena, but are masked by something not yet perceived." My own conclusion (1906, p. 72) was: "Booting is dominant, but usually imperfectly so." A more extended study has been desirable.

Booting is variable in amount. To indicate its degree I have had recourse to an artificial scale. I recognize 11 grades, running from 0 to 10. The grade 0 implies no feathers whatsoever. Grade 10 implies heavy booting extending over the front half of the shank. Grade 5 implies an extent of only half of the maximum, _i. e._, the outer front quarter of the shank. Intermediate grades indicate intermediate extension of the feathered area.

A. TYPES OF BOOTING.

The races of booted poultry used have been as follows: First, bantam Cochins of two varieties; second, a bantam Dark Brahma; and third, the Silkie. In my representatives of the first two groups, but particularly in the Dark Brahma, the amount of booting is variable. In one type the outer third of the shank in the newly hatched chick is covered by strong, heavy, specialized feathers, directed outward, while the middle and inner thirds are covered by smaller, finer, imbricating feathers sparsely placed and resembling reduced contour-feathers. In most individuals the transition from the one kind to the other is gradual, while in others it is sharp, and in a few the outer third only of the shank is feathered. In the Silkies, which the standard poultry books describe as being more sparsely feathered on the shank,[8] the outer zone of feathers is the only one developed; and, occasionally, as table 31 shows, even these feathers may be lacking. We have thus two types to distinguish--the extended (Cochin, Brahma) type and the restricted type.

[8] Thus Wright (1902) says the shanks of the Silkies (in England) are "slightly feathered," and Baldanus (1896) says that (in Germany) they are feathered on the _outer half_.

B. NORMAL VARIABILITY.

To appreciate the results of hybridizing we must first examine the variability of pure-blooded races. This is done in table 31.

TABLE 31.--_Distribution of boot-grades in the offspring of Cochin, Dark Brahma, and Silkie parents._

+---------------------------------------------------------------------------------------------+ | A. OFFSPRING OF COCHIN PARENTS. | +----+------------+------------+--------------------------------------------------------------+ | | Mother. | Father. | Grades of boot in offspring. | |Pen |-----+------+------+-----+----+---+----+----+----+----+----+----+----+----+----+--------+ |No. | | Boot-| |Boot-| | | | | | | | | | | | | | | No.| grade| No. |grade| 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 |Average.| +----+-----+------+------+-----+----+---+----+----+----+----+----+----+----+----+----+--------+ |848 | 2297| 10 | 545 | 10 |.. | ..| .. | 1 | .. | .. | 1 | .. | .. | 1 | 18 | 9.43 | |776 | 2574| 10 | 2732 | 8 |.. | ..| .. | .. | .. | .. | .. | .. | 3 | 2 | 6 | 9.27 | |848 | 2300| 8 | 545 | 10 |.. | ..| .. | .. | .. | .. | .. | .. | 1 | 2 | 5 | 9.25 | |776 | 2570| 6 | 2732 | 8 |.. | ..| .. | .. | .. | .. | 1 | 1 | .. | 11 | 1 | 8.71 | |848 | 2075| 9 | 545 | 10 |.. | ..| .. | .. | .. | 1 | 1 | .. | .. | .. | 4 | 8.50 | |776 | 2072| 6 | 2732 | 8 |.. | ..| .. | .. | .. | .. | 1 | .. | 4 | 2 | 2 | 8.44 | |758 | 130| 6 | 545 | 10 |.. | ..| .. | .. | .. | 1 | 1 | 1 | 3 | 9 | .. | 8.20 | |776 | 2073| 6 | 2732 | 8 |.. | ..| .. | .. | 1 | 2 | .. | 2 | 2 | 10 | 1 | 8.00 | |776 | 2300| 6 | 2732 | 8 |.. | ..| .. | .. | 1 | .. | 1 | 3 | 6 | 5 | 2 | 8.00 | |758 | 131| 10 | 545 | 10 |.. | ..| .. | .. | .. | 1 | .. | 4 | 6 | 1 | 1 | 7.96 | |776 | 2297| 6 | 2732 | 8 |.. | ..| .. | 1 | .. | 1 | .. | 3 | 6 | 6 | 2 | 7.95 | |776 | 1132| 3 | 2732 | 8 |.. | ..| .. | 1 | 1 | 1 | 1 | 3 | 6 | 8 | .. | 7.57 | |776 | 2937| 7 | 2732 | 8 |.. | ..| .. | .. | .. | .. | 1 | 3 | 3 | 1 | .. | 7.50 | |776 | 2299| 7 | 2732 | 8 |.. | ..| 1 | .. | .. | 1 | 1 | 4 | 7 | 3 | 1 | 7.44 | | +----|---+----+----+----+----+----+----+----+----+----+--------+ | Totals (199) |.. | ..| 1 | 3 | 3 | 8 | 9 | 24 | 47 | 61 | 43 | 8.24 | +------------------------------+----+---+----+----+----+----+----+----+----+----+----+--------+ | B. OFFSPRING OF DARK BRAHMA PARENTS. | | [All individuals have sprung from No. 121 ♀ (boot of grade 9) and No. 122 ♂ | | (boot of grade 6).] | +---------------------------------------------------------------------------------------------+ |816 | 2030| 6 | 122 | 6 | .. | ..| .. | .. | .. | .. | .. | .. | .. | 1 | 3 | 9.8 | |703 | 2030| 6 | 122 | 6 | .. | ..| .. | .. | .. | .. | 4 | 2 | 0 | 3 | 6 | 8.3 | |816 | 121| 6 | 122 | 6 | .. | ..| .. | .. | .. | .1 | 3 | 1 | 2 | 4 | 5 | 8.3 | |816 | 5979| 6 | 122 | 6 | .. | ..| .. | .. | .. | .. | 1 | 0 | 2 | .. | .. | 7.3 | |816 | 2353| 5 | 122 | 6 | .. | ..| .. | .. |[A]1| 1 | 1 | 0 | 1 | 0 | 2 | 7.1 | |816 | 5835| 5 | 122 | 6 | .. | ..| .. |[A]1| 0 | 1 | 2 | .. | .. | 1 | 3 | 6.5 | |816 | 5840| 5 | 122 | 6 | .. | ..| .. |[A]1| .. | .. | 1 | .. | .. | .. | 1 | 6.3 | |703 | 2353| 5 | 122 | 6 | .. | ..| .. | .. | 1 | 1 | 3 | .. | 1 | .. | .. | 5.8 | | +----+---+----+----+----+----+----+----+----+----+----+--------+ | Totals (61) | .. | ..| .. | 2 | 2 | 4 | 15 | 3 | 6 | 9 | 20 | 7.62 | +------------------------------+----+---+----+----+----+----+----+----+----+----+----+--------+ | C. OFFSPRING OF SILKIE PARENTS. | +----+-----+------+------+-----+----+---+----+----+----+----+----+----+----+----+----+--------+ |734 | 468| 4 | 774 | 3 | .. | ..| 1 | 2 | .. | .. | 1 | 1 | .. | .. | .. | 4.20 | |734 | 1002| 3 | 774 | 3 | .. | ..| 1 | 4 | .. | 1 | 3 | .. | .. | .. | .. | 4.11 | |734 | 841| (?)| 774 | 3 | .. | ..| .. | .. | 2 | .. | .. | .. | .. | .. | .. | 4.00 | |815 | 7434| 7 | 774 | 3 | .. | ..| .. | .. | 2 | .. | .. | .. | .. | .. | .. | 4.00 | |734 | 773| 1 | 774 | 3 | .. | ..| .. | 2 | 2 | .. | .. | .. | .. | .. | .. | 3.50 | |734 | 680| 1 | 774 | 3 | .. | ..| .. | 2 | .. | .. | .. | .. | .. | .. | .. | 3.00 | |734 | 405A| 1 | 774 | 3 | .. | ..| 1 | 3 | 1 | .. | .. | .. | .. | .. | .. | 3.00 | |815 | 499| 2 | 774 | 3 | 1 | 1| 3 | .. | .. | 2 | .. | 1 | .. | .. | .. | 3.00 | |734 | 499| 2 | 774 | 3 | 1 | 1| 5 | 2 | 2 | 1 | .. | .. | .. | .. | .. | 2.50 | |734 | 500| 1 | 774 | 3 | 2 | 1| 2 | 3 | .. | .. | .. | .. | .. | .. | .. | 1.75 | |815 | 773| 1 | 774 | 3 | 4 | 1| 3 | .. | .. | .. | .. | .. | .. | .. | .. | 1.25 | |815 | 500| 1 | 774 | 3 | 1 | 1| .. | .. | .. | .. | .. | .. | .. | .. | .. | 0.50 | |815 | 496| 3 | 774 | 3 | 1 | ..| .. | .. | .. | .. | .. | .. | .. | .. | .. | 0.00 | | +----+---+----+----+----+----+----+----+----+----+----+--------+ | Totals(68) | 10 | 5| 16 | 18 | 9 | 4 | 4 | 2 | .. | .. | .. | 2.72 | +------------------------------+----+---+----+----+----+----+----+----+----+----+----+--------+ | SUMMARY. | +------------------------------+--------------------------------------------------------------+ | | Grades of boot in offspring, reduced to percentages. | | Races. +----+---+----+----+----+----+----+----+----+----+----+--------+ | | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 |Average.| +------------------------------+----+---+----+----+----+----+----+----+----+----+----+--------+ |Cochins | .. | ..| 0.5| 1.5| 1.5| 4.0| 4.5|12.1|23.6|30.7|21.6| 8.24 | |Dark Brahmas | .. | ..| .. | 3.3| 3.3| 6.6|24.6| 4.9| 9.8|14.8|32.8| 7.62 | |Silkie |14.8|7.4|23.5|26.5|13.2| 5.9| 5.9| 2.9| .. | .. | .. | 2.72 | +------------------------------+----+---+----+----+----+----+----+----+----+----+----+--------+ [A] Determination made on embryo chicks.

An inspection of table 31 shows that, in respect to booting, the Cochins and Dark Brahmas are clearly closely related to each other. Owing to smaller numbers and to other circumstances that will be discussed later, the results are less regular in the Dark Brahma offspring, but in both the range is from 2 or 3 upward to 10, with a great preponderance in grades above 5. In the Silkies, on the other hand, the greatest frequency is found in grades below 5. This difference is correlated with a difference of the parents, for the commonest grades of the parents of the Cochins are between 6 and 10, of the Dark Brahmas between 5 and 9, and of the Silkies between 1 and 3. These results suggest that the Silkie is typically heterozygous in boot, producing 25 per cent recessives (boot of grade 4-7) and 75 per cent dominant (0, 1) and heterozygous (2, 3). We shall see that this hypothesis receives support from all Silkie matings.

Inside of any part of this table it appears that, on the whole, as the average grade of the boot in the progeny diminishes that of the parentage diminishes, although the correlation is by no means perfect. Thus the average of the parental grades in the first part of table 31, A (which is arranged in descending order of the averages of the offspring) is 8.5; in the lower half, 7.4. The average of parental grades in the upper half of table 31, B is 6.4; in the lower half 5.5. In table 31, C the grades are 2.9 and 2.3, respectively. This correlation indicates, without exactly measuring, heredity in grade of booting.

Table 32 shows the results of crosses between Cochins (high grade of boot) and Silkies (low grade).

TABLE 32.--_Distribution of boot-grades between a high and low grade of boot in parents._

+---------------------------------------------------------------------------------------------------+ | HIGH AND LOW GRADE OF BOOT IN PARENTS. | +---+-----------------------------+-----------------------+-----------------------------------------+ | | Mother. | Father. | Grade of boot in offspring. | |Pen|-----+----+-------------+----+-----+----+-------+----+--+--+--+--+--+--+--+--+--+--+--+--------+ |No.| | | | | | | | | | | | | | | | | | | | | | | No. |Gen.| Races. |Gra.| No. |Gen.| Race. |Gra.| 0| 1| 2| 3| 4| 5| 6| 7| 8| 9|10|Average.| +---+-----+----+-------------+----+-----+----+-------+----+--+--+--+--+--+--+--+--+--+--+--+--------+ |851| 5567| P | Bl. × Bf. C.| 9 | 7526| P | Silkie| 3 |..|..|..|..| 2|..|..|..| 3| 3| 5| 8.15 | |851| 3410| P | Do. | 9 | 7526| P | Do. | 3 |..|..|..|..|..| 4| 3| 2| 1| 6| 1| 7.29 | |851| 6956| P | Do. | 8 | 7526| P | Do. | 3 |..|..|..|..| 3| 3|..| 2| 2|..| 5| 7.13 | |851| 2073| P | Do. | 7 | 7526| P | Do. | 3 |..| 1|..| 1| 1|..| 1| 1| 1| 3| 2| 6.91 | |851| 2299| P | Do. | 7 | 7526| P | Do. | 3 |..|..|..|..| 2| 2| 1| 1|..|..| 3| 6.78 | |851| 840| P | Bf. C. | 10 | 7526| P | Do. | 3 |..|..|..|..| 1|..| 1|..|..| 1|..| 6.33 | |851| 1002| P | Do. | 8 | 7526| P | Do. | 3 |..|..|..| 3| 1| 2| 1| 2| 4| 1| 1| 6.27 | |815| 131| P | Bk. C. | 10 | 774| P | Do. | 4 |..|..|..| 3| 1| 1| 2| 2| 1| 1| 2| 6.23 | |851| 841| P | Bf. C. | 10 | 7526| P | Do. | 3 |..|..|..|..| 1|..| 1|..| 1|..|..| 6.00 | |851| 838| P | Do. | 8 | 7526| P | Do. | 3 |..|..|..| 4| 2| 4| 3|..|..| 2| 2| 5.65 | | |--+--+--+--+--+--+--+--+--+--+--+--------+ | Totals (116) | 0| 1| 0|11|14|16|13|10|13|17|21| 6.77 | +---------------------------------------------------------+--+--+--+--+--+--+--+--+--+--+--+--------+

So far as the average grade of boot in offspring goes, this table stands between that of the Cochins (table 31, A) and that of the Silkies (table 31, C). But what is especially striking is the apparent dimorphism revealed in the line of totals. There is one (empirical) mode at 10, corresponding with that of the Cochins, and a second clear mode at 5, corresponding to that of the Silkies. If we assume the Cochin to be homozygous in boot (RR) and the Silkie to be heterozygous in boot, then we can interpret the high mode as extracted recessives, the median mode as heterozygotes.

C. RESULTS OF HYBRIDIZATION.

We have next to consider the nature of the inheritance when one parent belongs to an unbooted race, the other to a booted one (table 33).

TABLE 33.--_Distribution of boot-grades in the F1 generation of booted × non-booted parents._

+------------------------------------------------------------------------------------------------------------------+ | A. COCHIN CROSSES. | +---+----------------------------+----------------------------+----------------------------------------------------+ |Pen| Mother. | Father. | Grade of boot in offspring. | |No.|----+----+-------------+----+-----+----+------------+----+---+---+---+---+---+---+---+---+---+---+---+--------+ | | No.|Gen.| Races. |Gra.| No. |Gen.| Races. |Gra.| 0| 1| 2| 3| 4| 5| 6| 7| 8| 9| 10|Average.| +---+----+----+-------------+----+-----+----+------------+----+---+---+---+---+---+---+---+---+---+---+---+--------+ |773|1334| P | W. Legh. | 0 | 836| P | Bl. Coch. | 10 | ..| ..| ..| 3| 1| 1| 1| 1| ..| 2| ..| 5.44 | |773| 193| P | Do. | 0 | 836| P | Do. | 10 | ..| 1| 2| 6| 8| 7| 4| 2| ..| ..| ..| 4.27 | |773|1366| P | Do. | 0 | 836| P | Do. | 10 | ..| ..| ..| 2| 5| 2| 1| ..| ..| ..| ..| 4.20 | |773| 127| P | Do. | 0 | 836| P | Do. | 10 | ..| ..| 3| 10| 9| 12| 4| ..| ..| ..| ..| 4.11 | |773| 692| P | W. Legh. (R)| 0 | 836| P | Do. | 10 | ..| ..| ..| 10| 3| 2| ..| ..| ..| ..| ..| 3.47 | |774|2075| P | Coch. | 8 | 1431| P |W. Legh. (R)| 0 | 6| 1| 1| ..| 1| ..| ..| ..| ..| ..| ..| 0.78 | | +---+---+---+---+---+---+---+---+---+---+---+--------+ | Totals (111) | 6| 2| 6| 31| 27| 24| 10| 3| 0| 2| 0| 3.91 | +-------------------------------------------------------------+---+---+---+---+---+---+---+---+---+---+---+--------+ | B. DARK BRAHMA CROSSES. | +---+----+----+-------------+----+-----+----+------------+----+---+---+---+---+---+---+---+---+---+---+---+--------+ |727| Y| P | D. Br. | 10 | 381| P | Houd. | 0 | ..| ..| ..| ..| 2| 3| 2| 1| 2| ..| ..| 5.80 | |727| 121| P | Do. | 10 | 381| P | Do. | 0 | 1| ..| ..| 1| 1| 5| 4| ..| ..| ..| ..| 4.67 | |823|2030| P | Do. | 7 | 3858| P | M × P | 0 | ..| ..| 5| 16| 15| 4| 1| 2| ..| ..| ..| 3.67 | |823| Y| P | Do. | 8 | 3858| P | Do. | 0 | ..| ..| 1| 7| 6| 2| ..| ..| ..| ..| ..| 3.56 | |838|3814| P | W. Legh. | 0 | 122| P | D. Br. | 6 | ..| 2| 2| 6| 6| 1| 1| ..| ..| ..| ..| 3.28 | |838| 202| P | Min. | 0 | 122| P | Do. | 6 | ..| ..| 2| 5| 3| ..| ..| ..| ..| ..| ..| 3.10 | |838| 71| P | W. Legh. | 0 | 122| P | Do. | 6 | ..| ..| ..| 1| ..| ..| ..| ..| ..| ..| ..| 3.00 | |838|3832| P | Do. | 0 | 122| P | Do. | 6 | 1| 1| ..| 1| 1| 2| ..| ..| ..| ..| ..| 3.00 | |838| 10| P | Do. | 0 | 122| P | Do. | 6 | ..| 1| ..| 3| 1| ..| ..| ..| ..| ..| ..| 2.80 | |816| 121| P | D. Br. | 9 | 4912| P | M × P | 0 | ..| ..| 8| 4| 1| 1| ..| ..| ..| ..| ..| 2.64 | |816|5838| P | Do. | 9 | 4912| P | Do. | 0 | ..| ..| 5| 5| 1| ..| ..| ..| ..| ..| ..| 2.64 | |838|5418| P | W. L., Min. | 0 | 122| P | D. Br. | 6 | 1| 1| 3| 3| 1| 1| ..| ..| ..| ..| ..| 2.50 | |816|5979| P | D. Br. | 6 | 4912| P | M × P | 0 | 4| 3| 4| 7| 4| 1| 1| ..| ..| ..| ..| 2.46 | |816|2353| P | Do. | 5 | 4912| P | Do. | 0 | ..| 2| 2| 4| 1| ..| ..| ..| ..| ..| ..| 2.44 | |816|5977| P | Do. | 4 | 4912| P | Do. | 0 | ..| 3| 2| 1| ..| 1| ..| ..| ..| ..| ..| 2.14 | |816|5835| P | Do. | 5 | 4912| P | Do. | 0 | 3| 5| 5| 8| 3| ..| ..| ..| ..| ..| ..| 2.12 | |816|5840| P | Do. | 5 | 4912| P | Do. | 0 | 5| 1| 3| 4| 1| ..| ..| ..| ..| ..| ..| 1.64 | |823|6626| P | Do. | 2 | 3858| P | Do. | 0 | 1| 10| 2| 2| ..| ..| ..| ..| ..| ..| ..| 1.33 | |816|5980| P | Do. | 5 | 4912| P | Do. | 0 | 5| 8| 1| 5| ..| ..| ..| ..| ..| ..| ..| 1.32 | | +---+---+---+---+---+---+---+---+---+---+---+--------+ | Totals (268) | 21| 37| 45| 83| 47| 21| 9| 3| 2| 0| 0| 2.84 | +-------------------------------------------------------------+---+---+---+---+---+---+---+---+---+---+---+--------+ | C. SILKIE CROSSES. | +---+----+----+-------------+----+-----+----+------------+----+---+---+---+---+---+---+---+---+---+---+---+--------+ |774| 777| P | Silkie. | 8 | 1176| P | W. Legh. | 0 | 3| ..| 1| 1| 1| ..| ..| ..| ..| ..| ..| 1.50 | |744| 681| P | Do. | 5 | 1176| P | Do. | 0 | 11| 2| 1| 1| 1| 1| ..| ..| ..| ..| ..| 0.94 | |744| 469| P | Do. | 1 | 1176| P | Do. | 0 | 11| 3| ..| ..| ..| ..| ..| ..| ..| ..| ..| 0.21 | | +---+---+---+---+---+---+---+---+---+---+---+-------- | Totals (37) | 25| 5| 2| 2| 2| 1| 0| 0| 0| 0| 0| 0.76 | +-------------------------------------------------------------+---+---+---+---+---+---+---+---+---+---+---+--------+ | SUMMARY. | +---------------------------------------+--------------------------------------------------------------------------- | | Grades of boot in offspring, reduced to percentages. | | Crosses. +-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+--------+ | | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 |Average.| +---------------------------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+--------+ |Cochin | 5.4| 1.8| 5.4| 28.0| 24.3| 21.6| 9.0| 2.7| 0.0| 1.8| ..| 3.91 | |Brahma | 7.8| 13.8| 16.8| 31.0| 17.5| 7.8| 3.4| 1.1| 0.7| ..| ..| 2.84 | |Silkie | 67.6| 13.5| 5.4| 5.4| 5.4| 2.7| ..| ..| ..| ..| ..| 0.76 | +---------------------------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+--------+

An inspection of Table 33, which gives the distribution of grades of boot in the offspring constituting the first hybrid generation, might well lead to the conclusion that inheritance is here of a blending nature, or that, if either condition is dominant, it is the booted one, as suggested in my report of 1906. On this hypothesis the offspring with no boot illustrate imperfection of dominance, and one would say that, in booting, dominance is very imperfect.

However plausible such an interpretation might appear when based on the first hybrid generation alone, it becomes untenable when subsequent generations are taken into account, as we shall see later. The hypothesis breaks down completely in the second hybrid generation and we are forced to the opposite hypothesis, namely, that the clean-shanked condition is dominant. Such an hypothesis would seem, at first, to contravene the principle enunciated in my report of 1906 that the more progressive condition is dominant over the less progressive condition, or absence. But such is not necessarily the fact. We have no right to assume that presence of boot is the new character. The rest of the body of poultry (save the head) is covered with feathers. If the foot is not it must be because there is something in the skin of the foot that inhibits the development of feathers there. And this inhibiting factor is dominant over its absence.

Table 33 shows that the Silkie crosses yield an exceptionally high per cent of the dominant clear-footed condition. This is additional evidence that the Silkies are DR, and so this cross produces 50 per cent of pure extracted dominants in addition to 50 per cent of heterozygotes in booting.

To get further light on the nature of inheritance of booting we pass to the examination of the second hybrid generation (table 34).

In the case of Silkies, which throw 67.6 per cent clean-shanked progeny in F1, we find in F2 only about 60 per cent clean-shanked. This diminution is, of course, due to the extraction of some pure booted recessives, which draw from the proportion of clean shanks.

In the case of the Cochins and Dark Brahmas, expectation, with perfect dominance, is that 75 per cent of the offspring shall be clean-shanked. Since dominance is imperfect (as shown by the occurrence of many booted birds in F1) we should look for an actual failure to reach so large a proportion, but we are hardly prepared for the result that in most of the F2 crosses of Cochins and Brahmas less than 25 per cent of the offspring are clean-shanked. In 4 pens the average is only 10 to 12 per cent, and in one only 2 per cent of the offspring fail to develop feathers on the feet. What shall we say of such a case as the last? The history of the father (No. 666) is absolutely certain; his mother was No. 121, the original Dark Brahma female, with a boot of grade 9 and a record in her immediate progeny that indicates perfect purity of booting in her germ-cells. His father was a White Leghorn with clean shanks and without a suspicion of having such antipodal blood as the Asiatic in his ancestry. No. 666 is certainly heterozygous in boot, if boot is a single unit. The hens with which No. 666 were mated were clearly heterozygous, as is known not only from their ancestry, but also from their behavior when mated with another cock, No. 254, in which case they threw 12 per cent non-booted offspring. If now both parents are heterozygous they must produce 25 per cent recessives. This is the fact that forces us to conclude that clean shank is not recessive, but dominant and due to an inhibitor that frequently _fails to dominate_. In table 31 the two recessive varieties, mated _inter se_, produce no featherless shanks; the feathers grow freely as they do over the rest of the body. Some of the Silkies of table 31, however, are really heterozygous, with the dominant inhibitor not showing; consequently they throw a large proportion of non-booted offspring. In F1, as table 33 shows, the heterozygous offspring have a reduced boot and perfect dominance--complete inhibition of boot--in from 6 to 68 per cent. Dominance is most complete in the Silkies, where, the feathering being feeble, the inhibitor has, as it were, less to do in overcoming it. In F2 the expected 75 per cent dominant is approached in the case of the Silkies (62 per cent and 59 per cent, respectively), but inhibition is very imperfect in the Cochin and Brahma crosses, being reduced to between 25 and 2 per cent. More proof that boot is due to the absence of a factor rather than to its presence is found in this generation. If absence of boot is recessive, then, combined with imperfection of dominance, _at least_ 25 per cent of the offspring should be recessive and probably a much larger proportion. The results in table 34 are absolutely incompatible with this hypothesis, since, in one case, there are only 2 per cent that can not develop boot. Two extracted clean-footed birds sometimes throw boot and sometimes not, and this result is to be expected on the hypothesis that clean-footedness is dominant, but two heavily booted birds can not transmit the boot inhibitor.

TABLE 34.--_Distribution of boot-grade in the F2 generation of booted × non-booted poultry._

+------------------------------------------------------------------------------------------------------------------+ | COCHIN CROSSES. | +---+---------------------------------------+-------------------------------------+--------------------------------+ | | Mother. | Father. | Offspring. | +---+---+-----+-----------------------------+---+----+---------------------+------+--------+-------+-------+-------+ |Pen|No.| Gen.| Races. | Grade.|No.|Gen.| Races. |Grade.| Boot | Boot | Boot | P. ct.| |No.| | | | | | | | |present.|slight.|absent.|absent.| +---+---+-----+---------------------+-------+---+----+-----+---------------+------+--------+-------+-------+-------+ |650|170| F1 |Bl. Coch. × Wh. Legh.| Pr. |265| F1 |Bl. Coch. × Wh. Legh.| Pr. | 19 | 2 | 2 | 8.7 | |650|263| F1 | Do. | Pr. |265| F1 | Do. | Pr. | 36 | 2 | 2 | 5.0 | |650|278| F1 | Do. | Pr. |265| F1 | Do. | Pr. | 26 | 4 | 4 | 11.8 | |650|361| F1 | Do. | Pr. |265| F1 | Do. | Pr. | 24 | 2 | 9 | 25.7 | |650|364| F1 | Do. | Pr. |265| F1 | Do. | Pr. | 39 | 5 | 3 | 6.4 | | | | | +--------+-------+-------+-------+ | | | | Totals (179) | 144 | 15 | 20 | 11.1 | | | | | | | | | | | | | | |========|=======|=======|=======| |654|602| F1 |Wh. Legh. × Bf. Coch.| Pr. |704| F1 |Wh. Legh. × Bf. Coch.| Pr. | 11 | 4 | 5 | 25.0 | |654|828| F1 | Do. | Pr. |704| F1 | Do. | Pr. | 7 | 11 | 0 | 0.0 | |654|640| F1 | Do. | Pr. |704| F1 | Do. | Pr. | 13 | 2 | 3 | 16.7 | |654|696| F1 | Do. | Pr. |704| F1 | Do. | Pr. | 8 | 5 | 8 | 38.1 | |654|767| F1 | Do. | Pr. |704| F1 | Do. | Pr. | 3 | 1 | 3 | 42.9 | |654|697| F1 | Do. | Pr. |704| F1 | Do. | Pr. | 4 | 3 | 6 | 46.2 | | | | | +--------+-------+-------+-------+ | | | | Totals (97) | 46 | 26 | 25 | 25.8 | +---+---+-----+-------------------------------------------------------------------+--------+-------+-------+-------+

TABLE 34.--_Distribution of boot-grade in the F2 generation of booted × non-booted poultry_--Continued.

+-------------------------------------------------------------------------------------------------------------------+ | DARK BRAHMA CROSSES. | +---+---------------------------------------+-------------------------------------+---------------------------------+ | | Mother. | Father. | Offspring. | |Pen+----+-----+---------------------+------+----+-----+------------------+-------+--------+-------+-------+--------+ |No.| No.| Gen.| Races. |Grade.| No.| Gen.| Races. |Grade. |Boot |Boot |Boot |P. ct. | | | | | | | | | | |present.|slight.|absent.|absent. | +---+----+-----+---------------------+------+----+----+-------------------+-------+--------+-------+-------+--------+ |608| 384| F1 |Wh. Legh. × Dk. Brah.| Pr. |409 |F1|Wh. Legh. × Dk. Brah.|Pr. | 36 | 5 | 3 | 6.8 | |608| 248| F1 | Do. | Pr. |409 |F1| Do. |Pr. | 32 | 5 | 4 | 9.8 | |608| 249| F1 | Do. | Pr. |409 |F1| Do. |Pr. | 39 | 11 | 13 | 20.6 | |608| 395| F1 | Do. | Pr. |409 |F1| Do. |Pr. | 20 | 11 | 10 | 24.4 | |608| 385| F1 | Do. | Pr. |409 |F1| Do. |Pr. | 20 | 6 | 14 | 35.0 | | | | | +--------+-------+-------+--------+ | | | | Totals (229) | 147 | 38 | 44 | 19.2 | | | | | +========+=======+=======+========+ |659| 762| F1 |Wh. Legh. × Dk. Brah.| Pr. |375 |F1|Wh. Legh. × Dk. Brah.|Pr. | 18 | 4 | 1 | 4.4 | |659| 503| F1 | Do. | Pr. |375 |F1| Do. |Pr. | 23 | 6 | 2 | 6.5 | |659| 382| F1 | Do. | Pr. |375 |F1| Do. |Pr. | 10 | 2 | 1 | 7.7 | |659| 250| F1 | Do. | Pr. |375 |F1| Do. |Pr. | 33 | 7 | 5 | 11.1 | |659| 737| F1 | Do. | Pr. |375 |F1| Do. Pr. | 19 | 2 | 3 | 12.5 | |659| 387| F1 | Do. | Pr. |375 |F1| Do. Pr. | 16 | 6 | 4 | 15.4 | | | | | +--------+-------+-------+--------+ | | | | Totals (162) | 119 | 27 | 16 | 9.9 | | | | | +========+=======+=======+========+ |655| 720| F1 |Wh. Legh. × Dk. Brah.| Pr. |666 |F1|Wh. Legh. × Dk. Brah.|Pr. | 5 | 2 | .. | 0.0 | |655| 724| F1 | Do. | Pr. |666 |F1| Do. |Pr. | 6 | 1 | .. | 0.0 | |655| 728| F1 | Do. | Pr. |666 |F1| Do. |Pr. | 3 | 1 | .. | 0.0 | |655| 730| F1 | Do. | Pr. |666 |F1| Do. |Pr. | 4 | .. | .. | 0.0 | |655| 732| F1 | Do. | Pr. |666 |F1| Do. |Pr. | 9 | .. | .. | 0.0 | |655| 734| F1 | Do. | Pr. |666 |F1| Do. |Pr. | 3 | .. | .. | 0.0 | |655| 761| F1 | Do. | Pr. |666 |F1| Do. |Pr. | 6 | 2 | .. | 0.0 | |655| 800| F1 | Do. | Pr. |666 |F1| Do. |Pr. | 1 | .. | .. | 0.0 | |655| 721| F1 | Do. | Pr. |666 |F1| Do. |Pr. | 9 | 1 | 1 | 9.1 | | | | | +--------+-------+-------+--------+ | | | | Totals (54) | 46 | 7 | 1 | 1.9 | | | | | +========+=======+=======+========+ |655| 724| F1 |Wh. Legh. × Dk. Brah.| Pr. |254 |F1|Wh. Legh. × Dk. Brah.|Pr. | 3 | .. | .. | 0.0 | |655| 734| F1 | Do. | Pr. |254 |F1| Do. |Pr. | 12 | 1 | .. | 0.0 | |655| 800| F1 | Do. | Pr. |254 |F1| Do. |Pr. | 13 | .. | 1 | 7.1 | |655| 720| F1 | Do. | Pr. |254 |F1| Do. |Pr. | 12 | .. | 1 | 7.7 | |655| 728| F1 | Do. | Pr. |254 |F1| Do. |Pr. | 8 | 1 | 1 | 10.0 | |655| 761| F1 | Do. | Pr. |254 |F1| Do. |Pr. | 17 | 4 | 4 | 16.0 | |655| 732| F1 | Do. | Pr. |254 |F1| Do. |Pr. | 8 | 1 | 2 | 18.2 | |655| 730| F1 | Do. | Pr. |254 |F1| Do. |Pr. | 7 | .. | 2 | 22.2 | |655| 721| F1 | Do. | Pr. |254 |F1| Do. |Pr. | 9 | .. | 3 | 25.0 | | | | | +--------+-------+-------+--------+ | | | | Totals (110) | 89 | 7 | 14 | 12.7 | | | | | +========+=======+=======+========+ |632| 742| F1 |Min. × Dk. Brah. | Pr. |637 |F1|Min. × Dk. Brah. |Pr. | 4 | 1 | 0 | 0.0 | |632| 690| F1 | Do. | Pr. |637 |F1| Do. |Pr. | 27 | 6 | 1 | 2.9 | |632| 631| F1 | Do. | Pr. |637 |F1| Do. |Pr. | 32 | 11 | 2 | 4.4 | |632| 618| F1 | Do. | Pr. |637 |F1| Do. |Pr. | 35 | 8 | 2 | 4.4 | |632| 700| F1 | Do. | Pr. |637 |F1| Do. |Pr. | 18 | 3 | 2 | 8.7 | |632| 703| F1 | Do. | Pr. |637 |F1| Do. |Pr. | 14 | 11 | 3 | 10.7 | |632| 743| F1 | Do. | Pr. |637 |F1| Do. |Pr. | 22 | 2 | 3 | 11.1 | |632| 599| F1 | Do. | Pr. |637 |F1| Do. |Pr. | 23 | 8 | 4 | 11.4 | |632| 524| F1 | Do. | Pr. |637 |F1| Do. |Pr. | 18 | 6 | 5 | 17.2 | |632| 576| F1 | Do. | Pr. |637 |F1| Do. |Pr. | 14 | 9 | 6 | 20.7 | |632| 638| F1 | Do. | Pr. |637 |F1| Do. |Pr. | 8 | 2 | 6 | 37.5 | | | | | +--------+-------+-------+--------+ | | | | Totals (316) | 215 | 67 | 34 | 10.8 | +---+----+-----+------------------------------------------------------------------+--------+-------+-------+--------+ +---+-------------------------------+--------------------------------+----------------------------------------------+ | | Mother. | Father. | Boot-grade in offspring. | |Pen+----+-----+----------------+---+----+-----+-----------------+---+--+--+--+--+--+--+--+--+--+--+--+-----+-------+ |No.| No.| Gen.| Races. |Gr.| No.| Gen.| Races. |Gr.| 0| 1| 2| 3| 4| 5| 6| 7| 8| 9|10|Aver-|P. ct. | | | | | | | | | | | | | | | | | | | | | | age.|absent.| +---+----+-----+----------------+---+----+-----+-----------------+---+--+--+--+--+--+--+--+--+--+--+--+-----+-------+ |801|2526| F1 |Min. × Dk. Brah.| 2 |5399| F1 |W. L. × Dr. Brah.| 8 |..|..|..|..| 1|..|..| 1|..|..| 1| 7.0 | 0.0 | |801|2831| F1 | Do. | 4 |5399| F1 | Do. | 8 | 1| 1| 1| 4| 1| 7| 2| 2| 2|..| 2| 5.0 | 4.3 | |801|1892| F1 | Do. | 3 |5399| F1 | Do. | 8 | 1| 1| 0| 1| 2|..| 1|..| 1| 1| 1| 5.0 |11.1 | | | | | +--+--+--+--+--+--+--+--+--+--+--+--+--+-------+ | | | | Totals (35) | 2| 2| 1| 5| 4| 7| 3| 3| 3| 1| 4| 5.2 | 5.71 | +---+----+-----+-----------------------------------------------------+--+--+--+--+--+--+--+--+--+--+--+-----+-------+

TABLE 34.--_Distribution of boot-grade in the F2 generation of booted × non-booted poultry_--Continued.

+-------------------------------------------------------------------------------------------------------------------+ | SILKIE CROSSES. | +---+-------------------------------+-------------------------------+-----------------------------------------------+ | | Mother. | Father. | Boot-grade in offspring. | |Pen+----+-----+----------------+---+----+-----+----------------+---+---+--+--+--+--+--+--+--+--+--+--+-----+-------+ |No.| No.| Gen.| Races. |Gr.| No.| Gen.| Races. |Gr.| 0| 1| 2| 3| 4| 5| 6| 7| 8| 9|10|Aver-|P. ct. | | | | | | | | | | | | | | | | | | | | | | age.|absent.| +---+----+-----+----------------+---+----+-----+----------------+---+---+--+--+--+--+--+--+--+--+--+--+-----+-------+ |709|1955| F1 |Silkie × Spanish| 5 |1578| F1 |Silkie × Spanish| 0 | 5| 1| 2| 1| 1| 1| 1| 0| 0| 0| 0| 1.92| 41.7 | |753|1966| F1 |Silkie × Min | 0 |2573| F1 |Min. × Silkie | 0 | 19| 4| 2| 2|..| 2| 2| 2| 1|..|..| 1.71| 55.9 | |709|1963| F1 |Silkie × Spanish| 7 |1578| F1 |Silkie × Spanish| 0 | 23| 6| 1| 6| 7|..|..|..|..|..|..| 1.26| 53.5 | |753|2575| F1 |Silkie × Min | 0 |2573| F1 |Silkie × Min. | 0 | 15| 3| 7|..|..|..|..|..|..|..|..| 0.68| 60.0 | |753|2071| F1 | Do. | 0 |2573| F1 | Do. | 0 | 23| 4| 6|..|..|..|..|..|..|..|..| 0.49| 69.7 | |709|1453| F1 | Do. | 1 |1578| F1 |Silkie × Spanish| 0 | 24|11| 3|..|..|..|..|..|..|..|..| 0.45| 63.2 | |709|2223| F1 |Silkie × Spanish| 0 |1578| F1 | Do. | 0 | 32| 7| 3|..|..|..|..|..|..|..|..| 0.31| 76.2 | | | | | +---+--+--+--+--+--+--+--+--+--+--+-----+-------+ | | | | Totals (227) |141|36|24| 9| 8| 3| 3| 2| 1| 0| 0| 0.87| 62.2 | | | | | |===+==+==+==+==+==+==+==+==+==+==+=====+=======+ |830|4082| F1 |Silkie × W. Legh| 2 |3947| F1 |Silkie × W. Legh| 1 | 11| 8|..| 7| 1|..|..|..|..|..|..| 1.22| 40.7 | |830|4079| F1 | Do. | 0 |3947| F1 | Do. | 1 | 18| 7| 6| 3|..|..|..|..|..|..|..| 0.82| 53.0 | |830|5379| F1 | Do. | 0 |3947| F1 | Do. | 1 | 18| 4| 5| 3|..|..|..|..|..|..|..| 0.77| 60.0 | |830|4081| F1 | Do. | 0 |3947| F1 | Do. | 1 | 24| 6|10| 1|..|..|..|..|..|..|..| 0.71| 58.5 | |830|5374| F1 | Do. | 0 |3947| F1 | Do. | 1 | 11| 3| 3| 1|..|..|..|..|..|..|..| 0.67| 61.1 | |830|3946| F1 | Do. | 0 |3947| F1 | Do. | 1 | 19| 1|..|..| 1|..|..|..|..|..|..| 0.24| 90.5 | | | | | |===+==+==+==+==+==+==+==+==+==+==+=====+=======+ | | | | Totals (170) |101|29|24|14| 2| 0| 0| 0| 0| 0| 0| 0.75| 59.4 | +---+----+-----+----------------------------------------------------+---+--+--+--+--+--+--+--+--+--+--+-----+-------+

The distribution of table 35 is characterized by its large variability. Although the numbers are small, there are evidences of two modes, one between grades 3 and 6, and the other at from 8 to 10; these evidently correspond to the modes of the typical Silkie and the typical Cochin respectively or to DR and RR types of booting respectively. The distribution of table 35 is additional evidence of the heterozygous nature of the Silkie boot.

TABLE 35.--_Distribution of boot-grades in Silkie × Cochin crosses._

+---+------------------------------+--------------------------------+-----------------------------------------------------------+ | | Mother. | Father. | Boot-grades in offspring. | |Pen+----+----+--------------+-----+------+----+--------------+-----+--+---+---+---+---+---+---+---+---+---+----+-----+---------+ |No.| No.|Gen.| Races. | Gra.| No. |Gen.| Races. | Gra.| 0| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | Av. | P. ct. | | | | | | | | | | | | | | | | | | | | | | | abs. | +---+----+----+--------------+-----+------+----+--------------+-----+--+---+---+---+---+---+---+---+---+---+----+-----+---------+ |821|5925| F1 | Silk. × Coch.| 7 | 6095 | F1 | Silk. × Coch.| 7 |..| ..| ..| ..| 1 |.. | ..| 1 | 3 | 1 | 1 | 7.7 | 0.0 | |821|7408| F1 | Do. | 4 | 6095 | F1 | Do. | 7 |..| ..| ..| 1| 2 | 2 | 3 | ..| 2 | 1 | 2 | 6.5 | 0.0 | |821|7413| F1 | Do. | 3 | 6095 | F1 | Do. | 7 | 2| 0| 3| 1| 0 | 1 | 1 | 0 | 0 | 1 | 1 | 3.9 | 20.0 | |821|7416| F1 | Do. | 5 | 6095 | F1 | Do. | 7 |..| ..| ..| 3| 1 | 0 | 4 | 0 | 3 | 3 | 2 | 6.8 | 0.0 | |821|7417| F1 | Do. | .. | 6095 | F1 | Do. | 7 |..| ..| ..| ..|.. |.. | ..| 1 |.. | 1 | 4 | 9.3 | 0.0 | |821|7418| F1 | Do. | 4 | 6095 | F1 | Do. | 7 |..| ..| 1| ..| 2 | 1 | 1 | 1 | 1 |.. | 1 | 5.8 | 0.0 | |821|7423| F1 | Do. | 6 | 6095 | F1 | Do. | 7 |..| ..| ..| 1|.. | 2 | ..| 2 | 2 |.. | 2 | 7.0 | 0.0 | |821|7428| F1 | Do. | .. | 6095 | F1 | Do. | 7 | 1| ..| ..| ..|.. | 1 | ..| ..| 1 |.. |.. | 4.3 | 33.3 | |821|7429| F1 | Do. | 8 | 6095 | F1 | Do. | 7 |..| ..| ..| 1| 1 | 1 | ..| ..|.. | 1 | 1 | 6.2 | 0.0 | | | | | +--+----+--+---+---+---+---+---+---+---+----+-----+---------+ | | | | Totals (77) | 3| 0| 4| 7| 7 | 8 | 9 | 5 |12 | 8 |14 |6.42 | 3.90 | | | | | |\--------------------/|\------------------/| | | | | | | | 29 | 48 | | | +---+----+----+-----------------------------------------------------+----------------------+--------------------+-----+---------+

We are now in a position to consider the effect of back crosses (table 36). The contrast between the totals in tables 36 and 37 is very great. The strict Mendelian expectation is: in the DR × D crosses 50 per cent DD (clean-footed) and 50 per cent heterozygous, which, with imperfect dominance, might be expected to show foot-feathering. Actually about 46 per cent are clean-footed. In the DR × R crosses expectation is that 50 per cent certainly (the extracted recessives) and 50 per cent more possibly will have the shanks feathered, on account of imperfect dominance of the heterozygotes. Actually all have feathered feet. These statistics thus confirm the view of the dominance of the inhibiting factor. Were clean shank recessive, then the DR × R crosses must give 50 per cent clean-footed and probably over. The actual result, none clean-footed, is not in accord with the latter assumption.

TABLE 36.--_Distribution of boot-grade in DR × D (non-booted) crosses._

+---+-----------------------------------------+---------------------------+--------------------------------------+ | | Mother. | Father. | Boot-grade in offspring. | | +---+-----+----------------------+--------+---+----+---------+--------+---------+--------+--------+----------+ |Pen| | | | | | | | | | | | | |No.|No.| Gen.| Races. | Grade. |No.|Gen.| Race. | Grade. | Present.| Slight.| Absent.| Per cent.| | | | | | | | | | | | | | present. | +---+---+-----+----------------------+--------+---+----+---------+--------+---------+--------+--------+----------+ |653|508| F1 | Wh. Legh. × Bf. Coch.| Pr. |117| P. | Game. | 0 | 3 | 4 | 6 | 46.2 | |653|508| F1 | Do. | Pr. |116| P. | Do. | 0 | 6 | 5 | 4 | 26.7 | |653|577| F1 | R × Bf. Coch. | 3 |117| P. | Do. | 0 | 1 | 0 | 7 | 87.5 | |653|577| F1 | Do. | 3 |116| P. | Do. | 0 | 1 | 3 | 2 | 33.3 | |653|587| F1 | Do. | 1 |117| P. | Do. | 0 | 1 | 2 | 4 | 57.1 | |653|587| F1 | Do. | 1 |116| P. | Do. | 0 | 3 | 3 | 2 | 25.0 | |653|635| F1 | Do. | 3 |117| P. | Do. | 0 | .. | 1 | 6 | 85.7 | |653|635| F1 | Do. | 3 |116| P. | Do. | 0 | 2 | 2 | 1 | 20.0 | |653|652| F1 | Do. | 5 |117| P. | Do. | 0 | 5 | 8 | 4 | 23.5 | |653|652| F1 | Do. | 5 |116| P. | Do. | 0 | 1 | 2 | 2 | 40.0 | |653|691| F1 | Do. | Pr. |117| P. | Do. | 0 | 2 | 2 | 1 | 20.0 | |653|705| F1 | Do. | 2 |117| P. | Do. | 0 | 3 | 2 | 5 | 50.0 | |653|705| F1 | Do. | 2 |116| P. | Do. | 0 | 1 | 1 | 5 | 71.4 | |653|713| F1 | Do. | Pr. |117| P. | Do. | 0 | .. | 0 | 4 | 100.0 | |653|713| F1 | Do. | Pr. |116| P. | Do. | 0 | 1 | 1 | 3 | 60.0 | |653|760| F1 | Do. | Pr. |117| P. | Do. | 0 | 2 | 2 | 6 | 60.0 | |653|760| F1 | Do. | Pr. |116| P. | Do. | 0 | 0 | 3 | 2 | 40.0 | |653|799| F1 | Do. | 3 |117| P. | Do. | 0 | 2 | 0 | 3 | 60.0 | | | | | +---------+--------+--------+----------+ | | | | Total (143) | 34 | 42 | 67 | 46.9 | | | | | |======================================= |661|635| F1 | Bf. Coch. × Game. | Pr. |466| P. | Game. | 0 | 1 | .. | 2 | 66.7 | |661|635| F1 | Do. | Pr. |428| P. | Do. | 0 | 2 | .. | 1 | 33.3 | |661|691| F1 | Do. | Pr. |466| P. | Do. | 0 | 2 | .. | 2 | 50.0 | |661|691| F1 | Do. | Pr. |428| P. | Do. | 0 | 2 | .. | 1 | 33.3 | |661|799| F1 | Do. | Pr. |466| P. | Do. | 0 | 3 | .. | 2 | 40.0 | |661|799| F1 | Do. | Pr. |428| P. | Do. | 0 | 4 | .. | 1 | 20.0 | | | | | +---------+--------+--------+----------+ | | | | Total (23) | 14 | 0 | 9 | 39.1 | | | | | Grand Total (166) | 48 | 42 | 76 | 45.8 | +-------+-----+-----------------------------------------------------------+---------+--------+--------+----------+

TABLE 37.--_Distribution of boot-grade in DR × RR (booted) crosses._

+----+--------------------+-----+------------------------------+---------------------------------------------+----+ | | Mother. | | Father. | Boot-grade in offspring. | | | +-----+-----+--------+-----+-----+--------+----------+----+---+---+---+---+----+----+----+----+----+----+----+ |Pen | | | | | | | | | | | | | | | | | | | | |No. | | | | | | | | | | | | | | | | | | | | | | No. | Gen.| Race. | Gr. | No. | Gen. | Race. | Gr.| 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | +----+-----+-----+--------+-----+-----+--------+----------+----+---+---+---+---+----+----+----+----+----+----+----+ |851 | 838 | P. | Cochin.| 8 |7526 |[A]F1 | Silkie. | 3 |.. |.. |.. | 3 | 2 | 4 | 3 | .. | .. | 2 | 2 | |851 | 840 | P. | Do. | 10 |7526 | F1 | Do. | 3 |.. |.. |.. |.. | 1 | .. | 1 | .. | .. | 1 | .. | |851 | 841 | P. | Do. | 10 |7526 | F1 | Do. | 3 |.. |.. |.. |.. | 1 | .. | 1 | .. | 1 | .. | .. | |851 |1002 | P. | Do. | 8 |7526 | F1 | Do. | 3 |.. |.. |.. | 3 | 1 | 2 | 1 | 2 | 3 | 1 | 1 | |851 |2073 | P. | Do. | 7 |7526 | F1 | Do. | 3 |.. |.. | 1 | 1 | 1 | .. | 1 | 1 | 1 | 3 | 2 | |851 |2299 | P. | Do. | 9 |7526 | F1 | Do. | 3 |.. |.. |.. |.. | 2 | 2 | 1 | 1 | .. | .. | 2 | |851 |3410 | P. | Do. | 9 |7526 | F1 | Do. | 3 |.. |.. |.. |.. | .. | 4 | 3 | 2 | 1 | 5 | 1 | |851 |5567 | P. | Do. | 9 |7526 | F1 | Do. | 3 |.. |.. |.. |.. | 2 | .. | .. | .. | 3 | 3 | 5 | |851 |6956 | P. | Do. | 8 |7526 | F1 | Do. | 3 |.. |.. |.. |.. | 3 | 3 | .. | 2 | 2 | .. | 5 | | | | | ==================================================== | | | | Totals (99) ..... | 0 | 0 | 1 | 7 | 13 | 15 | 11 | 8 | 11 | 15 | 18 | +----+-----+-----+---------------------------------------------+---+---+---+---+----+----+----+----+----+---------+ [A] Pure-blooded Silkie assumed heterozygous to boot.

Numerous observations have been made upon the progeny of parents belonging to hybrid generations beyond the first. Owing to the extreme imperfection of dominance it is rarely possible to say with certainty from inspection whether a given bird has germ-cells dominant or recessive, or both, with reference to booting; only breeding enables us to make a decision. There is an exception, however, in the case of pure extracted recessives. They are distinguished by heavy booting and produce only booted offspring. I propose to give, in detail, the matings of these later generations and their progeny, the families being arranged in decreasing order of average grade of booting (table 38).

TABLE 38.--_Distribution of boot-grades in offspring of parents one or both of which belong to a hybrid generation beyond the first._

B = Brahma; C = Cochin; G = Game; L = Leghorn; M = Minorca; S = Silkie; Sp = Spanish; T = Tosa; WL = White Leghorn

+------+---+------------------------+------------------------+-------+-------------------------------------+ |Serial|Pen| Mother. | Father. |Mating.| Boot-grade in offspring. | | No. |No.+----+-----+---------+---+----+-----+---------+---+ +--+--+--+--+--+--+--+--+--+--+--+----+ | | | No.| Gen.| Races. |Gr.| No.| Gen.| Races. |Gr.| | 0| 1| 2| 3| 4| 5| 6| 7| 8| 9|10| Av.| +------+---+----+-----+---------+---+----+-----+---------+---+-------+--+--+--+--+--+--+--+--+--+--+--+----+ | 1 |814| 354| F1 |B × T | 7|3975| F2 |B × T | 9 |R × R |..|..|..|..|..|..|..|..|..|10|15|9.6 | | 2 |801| 181| F1 | Do. | 4|5399| F2 |M × B | 8 | Do. |..|..|..|..|..|..|..|..|..| 1| 1|9.5 | | 3 |814| 300| F1 | Do. | 5|3975| F2 |B × T | 9 | Do. |..|..|..|..|..|..|..|..| 1| 3| 4|9.4 | | 4 |801|4569| F2 | Do. | 6|4562| F2 | Do. | 7 | Do. |..|..|..|..|..|..|..|..| 1| 1| 2|9.3 | | 5 |814|5523| F2 | Do. | 9|3975| F2 | Do. | 9 | Do. |..|..|..|..|..| 1|..|..| 3| 4| 9|9.1 | | 6 |814|4560| F2 | Do. | 8|3975| F2 | Do. | 9 | Do. |..|..|..|..|..| 1| 1| 1|..| 2| 7|8.8 | | 7 |814| 190| F1 | Do. | 2|3975| F2 | Do. | 9 | Do. |..|..|..|..|..|..| 1| 1| 1| 1| 4|8.8 | | 8 |806|4325| F3 |M × B | 7|5257| F3 |M × B | 9 | Do. |..|..|..|..|..|..| 1| 1| 2| 2| 3|8.6 | | 9 |806|5913| F3 | Do. | 7|5257| F3 | Do. | 9 | Do. |..|..|..|..| 1|..|..| 1| 4| 2| 3|8.3 | | 10 |732|1235| F2 | Do. | 8|2732| F2 | Do. | 6 | Do. |..|..|..|..|..|..| 1| 2| 4| 3|..|7.9 | | 11 |806|4052| F3 | Do. | 5|5257| F3 | Do. | 5 | Do. |..|..|..|..| 1| 1|..| 3|..| 6| 1|7.8 | | 12 |776|1132| F2 |C × WL | 3|2732| P. |C | 8 |DR × R |..|..|..| 1| 1| 1| 1| 3| 6| 8|..|7.6 | | 13 |801|6869| F1.5|B × F1 | 6|4562| F2 |M × B | 7 |R × R |..|..|..|..|..| 1| 1| 2| 1| 1| 1|7.4 | | 14 |814| 186| F1 |T × B | 4|3975| F2 |B × T | 9 |DR × R |..| 2| 1| 0| 1| 3| 0| 1| 3| 6| 5|7.2 | | 15 |814|4683| F2 | Do. | 2|3975| F2 | Do. | 9 | Do. |..|..|..|..| 3| 2| 3| 1| 1| 1| 5|7.1 | | 16 |767|2104| F2 |WL × B | 3|3116| F1 | Do. | 9 | Do. |..|..|..| 1| 4| 1| 2| 7| 6| 1| 0|7.1 | | 17 |801|2526| F1 | Do. | 2|5399| F2 |M × B | 8 | Do. |..|..|..|..| 1|..|..| 1|..|..| 1|7.0 | | 18 |806|3936| F2 |M × B | 10|5257| F3 | Do. | 9 |R × R |..|..|..|..| 1|..| 2|..| 2|..| 1|7.0 | | 19 |839|5383| F2 |L × M × B| 2|4348| F2 |L × M × B| 3 |DR × DR|..|..|..|..| 1| 1|..|..|..| 1| 1|7.0 | | 20 |801|5515| F2 |B × T | 4|5399| F2 |M × B | 8 |DR × R |..|..|..| 1| 1| 2| 2|..| 1| 1| 3|6.9 | | 21 |732|1003| F2 |M × B | 9|2442| F2 | Do. | 6 |R × R |..|..|..|..| 3| 7| 7| 7| 7| 5| 2|6.8 | | 22 |839|1892| F1.5|L × M × B| 6|4348| F2 |L × M × B| 3 |R × DR |..|..|..| 2| 1|..| 1|..|..| 2| 2|6.8 | | 23 |806|4196| F3 |M × B | 2|5257| F3 |M × B | 9 |DR × R |..|..|..| 2| 2| 2| 1|..|..| 3| 3|6.7 | | 24 |801|2526| F1 |WL × B | 2|5399| F2 | Do. | 8 | Do. |..|..|..|..| 1|..|..| 1|..| 1| 0|6.7 | | 25 |801|6861| F2.5|B × T | 7|4562| F2 | Do. | 7 |R × R |..|..|..|..|..| 2| 1|..|..|..| 1|6.5 | | 26 |767| 872| F2 | Do. | 5|3116| F1 |B × T | 9 |DR × R | 1| 0| 0| 1| 4| 6| 9| 4| 4| 6| 3|6.5 | | 27 |801|4263| F2 | Do. | 3|4562| F2 |M × B | 7 | Do. |..|..|..| 2| 3|..| 3| 1| 1| 4| 1|6.5 | | 28 |767| 181| F1 | Do. | 4|3166| F1 |B × T | 9 | Do. |..|..| 1| 2| 6|13|11| 5|11| 8| 3|6.5 | | 29 |814| 862| F2 | Do. | 1|3975| F2 | Do. | 9 | Do. |..|..|..| 2| 2| 5| 2| 1| 1| 3| 2|6.3 | | 30 |801| 872| F2 | Do. | 5|5399| F2 |M × B | 8 | Do. |..|..|..| 1| 3| 8| 5| 2|..| 2| 4|6.3 | | 31 |839|5389| F2 |M × B | 7|4348| F2 | Do. | 3 |R × DR |..|..|..| 6| 4| 1| 0| 1| 1| 1| 6|6.2 | | 32 |801| 872| F2 |B × T | 5|4562| F2 | Do. | 7 |DR × R |..|..|..| 1| 5| 4| 3| 1| 2| 2| 2|6.1 | | 33 |767| 190| F1 | Do. | 4|3116| F1 |B × T | 9 | Do. |..|..|..| 5| 6|11|12| 7| 4| 9|..|6.1 | | 34 |801|1892| F1 |M × B | 3|4562| F2 |M × B | 7 | Do. |..|..| 1|..|..|..| 1|..| 2|..|..|6.0 | | 35 |801|5515| F2 |B × T | 4|4562| F2 | Do. | 7 | Do. |..|..| 1|..|..| 1| 3|..| 1| 1|..|6.0 | | 36 |731| 248| F1 |M × B | 4|1249| F2 |WL × B | 7 | Do. |..|..| 2| 3| 3|..| 2|..|..| 5| 2|6.0 | | 37 |732|1228| F2 | Do. | 8|2442| F2 |M × B | 6 |R × R |..|..|..| 2| 8| 5| 6| 2| 8| 3|..|6.0 | | 38 |732| 690| F1 | Do. | 5|2442| F2 | Do. | 6 |DR × R | 2| 0| 6| 2| 5| 5| 7|16|10| 6|..|6.0 | | 39 |751|1919| F2 |WL × B | 8|1139| F2 |L × B | 8 |R × R |..|..|..| 5| 4| 6| 6| 1|11| 1|..|5.9 | | 40 |732| 618| F1 |M × B | 8|2442| F2 |M × B | 6 |DR × R |..| 1| 2| 3| 2| 5| 3| 5| 9| 1|..|5.8 | | 41 |731|1245| F2 |WL × B | 9|1249| F2 |WL × B | 7 |R × R |..|..| 1| 2| 1| 8| 2| 3| 6|..|..|5.8 | | 42 |760| 354| F1 |B × T | 5|1270| F2 |B × T | 2 |R × DR |..|..| 1| 3| 9| 5| 8| 4| 7| 2|..|5.7 | | 43 |701|1915| F2 |WL × B | 8|1898| F2 |WL × B | 3 | Do. |..|..|..|..| 7| 4| 3| 2| 3| 1|..|5.7 | | 44 |801|6869| F1.5|B (M × B)| 6|5399| F2 | Do. | 8 |DR × R |..|..|..| 1|..| 1|..|..|..| 1|..|5.7 | | 45 |801|4570| F2 |B × T | 2|4562| F2 | Do. | 7 | Do. |..|..| 1| 2| 5| 3| 1| 1| 1| 4|..|5.6 | | 46 |814| 703| F1 | Do. | 4|3975| F2 |B × T | 9 | Do. |..|..| 3| 5| 2| 7| 5| 6| 2| 4|..|5.5 | | 47 |732| 953| F2 |M × B | 3|2442| F2 |M × B | 6 | Do. |..| 2| 2| 3| 8| 9| 5| 3| 7| 6|..|5.5 | | 48 |801|7528| F1 | Do. | 4|4562| F2 | Do. | 8 | Do. |..|..|..| 1| 4| 2| 1|..| 1|..| 1|5.3 | | 49 |731|2116| F2 | Do. | 10|1249| F2 |WL × B | 7 |R × R |..| 1| 1| 1| 2| 3| 0| 2| 2| 1|..|5.2 | | 50 |745|2115| F2 |C × T | 4|1258| F2 |B × T | 4 |DR × DR|..|..|..| 2| 1| 6| 4| 2|..|..|..|5.2 | | 51 |801|6843| F2 |B × T | 3|4562| F2 | Do. | 8 |DR × R |..|..|..|..| 3| 2| 1|..| 1|..|..|5.1 | | 52 |801|2831| F1 |M × B | 4|5399| F2 | Do. | 8 | Do. | 1| 1| 1| 4| 1| 7| 2| 2| 2|..| 2|5.0 | | 53 |801|1892| F1 | Do. | 3|5399| F2 | Do. | 8 | Do. | 1| 1|..| 1| 2|..| 1| 0| 1| 1| 1|5.0 | | 54 |801|7528| F1 | Do. | 4|4562| F2 | Do. | 8 | Do. |..|..|..| 1| 2| 1| 1|..| 1|..|..|5.0 | | 55 |731|1755| F2 |WL × B | 6|1249| F2 |WL × B | 7 |R × R |..|..|..|..| 2| 1| 4| 1| 2|..|..|5.0 | | 56 |745|2513| F3 |C × T | 4|1258| F2 |B × T | 4 |DR × DR|..|..|..|..| 2| 5| 2|..| 3| 1|..|5.0 | | 57 |839|3950| F2 |M × B | 4|4348| F2 |M × B | 3 | Do. |..| 2| 3| 3| 2| 4| 1| 1| 1| 2| 2|4.95| | 58 |754| 873| F2 |B × T | 3| 871| F2 |B × T | 2 | Do. | 1| 2| 1| 4| 1|..|..|..| 8|..|..|4.94| | 59 |806| 599| F2 |M × B | 3|5257| F2 |M × B | 7 |DR × R |..|..| 2| 1| 2| 2| 1|..| 1|..|..|4.86| | 60 |760| 300| F1 |B × T | 7|1270| F2 |B × T | 2 |R × DR |..|..| 2|19| 8|13| 6| 4| 5| 2| 1|4.83| | 61 |806|4456| F2 |M × B | 1|5257| F3 |M × B | 7 |DR × R |..| 1| 1| 1| 1|..| 1|..| 1| 1|..|4.71| +------+---+----+-----+---------+---+----+-----+---------+---+-------+--+--+--+--+--+--+--+--+--+--+--+----+

TABLE 38.--_Distribution of boot-grades in offspring of parents one or both of which belong to a hybrid generation beyond the first_--Continued.

B = Brahma; C = Cochin; G = Game; L = Leghorn; M = Minorca; S = Silkie; Sp = Spanish; T = Tosa; WL = White Leghorn. +------+---+------------------------+-----------------------+--------+--------------------------------------+ | | | Mother. | Father. | | Boot-grade in offspring. | |Serial|Pen|----+-----+---------+---+----+-----+--------+---+ Mating.+--+--+--+--+--+--+--+--+--+--+--+-----+ | No. |No.| No.| Gen.| Races. |Gr.| No.| Gen.| Races. |Gr.| | 0| 1| 2| 3| 4| 5| 6| 7| 8| 9|10| Av. | +------+---+----+-----+---------+---+----+-----+--------+---+--------+--+--+--+--+--+--+--+--+--+--+--+-----+ | 62 |732|2407| F2 |M × B | 2|2442| F2 |M × B | 6 | DR × R |..|..| 1| 3| 4| 1| 1| 2|..| 1|..| 4.69| | 63 |701| 894| F2 |L × B | 7|1898| F2 |L × B | 3 | R × DR | 1| 1| 2| 8| 6| 1| 2| 2| 4| 2|..| 4.62| | 64 |760| 994| F2 |B × T | 3|1270| F2 |B × T | 3 | DR × DR|..|..|..|..| 4| 2| 1|..|..|..|..| 4.57| | 65 |760| 981| F2 | Do. | 3|1270| F2 | Do. | 3 | Do. | 1|..| 3| 6| 1| 4| 2| 7|..|..|..| 4.54| | 66 |701|1772| F2 |L × B | 6|1898| F2 |L × B | 3 | R × DR |..|..|..| 4| 7| 2| 2| 2|..|..|..| 4.47| | 67 |839|3541| F1 |M × B | 6|4348| F2 |M × B | 3 | DR × DR| 4| 1| 4|..|..| 4| 2|..| 2| 1| 2| 4.30| | 68 |842|1645| F2 | Do. | 2|4385| F2 | Do. | 4 | Do. | 3| 2| 6| 5| 6| 6| 3| 0| 2| 4| 1| 4.29| | 69 |770|2049| F2 |L × B | 3| 926| F2 | Do. | 3 | Do. | 9| 3| 1| 6| 8| 2| 6| 6| 3| 1| 3| 4.29| | 70 |731|2577| F1.5|L × C | 4|1249| F2 |L × B | 7 | DR × R |..|..| 2| 2| 3| 2| 2| 1|..|..|..| 4.25| | 71 |701| 250| F1 |L × B | 3|1898| F2 | Do. | 3 | DR × DR| 3| 3| 5| 8|12|10|10| 6| 1|..|..| 4.22| | 72 |701|1335| F2 |T × L × B| 8|1898| F2 | Do. | 3 | R × DR |..|..| 1| 9| 6| 6| 4| 1|..|..|..| 4.22| | 73 |806|4767| F3 |M × B | 3|5257| F3 |M × B | 7 | DR × R |..|..| 1|..| 2| 1| 1|..|..|..|..| 4.20| | 74 |740|1439| F2 |C × L | 2|1145| F2 |C × L | 3 | DR × DR| 3|..| 1| 3| 6| 4| 2|..| 2| 1|..| 4.18| | 75 |754|3126| F2 |B × T | 4| 871| F2 |B × T | 3 | Do. |..| 2| 5|11| 7|10| 5| 0| 2| 1|..| 4.14| | 76 |770|1645| F2 |M × B | 4| 926| F2 |M × B | 3 | Do. | 3| 2| 1| 9| 5| 5| 2| 2| 3| 1|..| 4.10| | 77 |731| 249| F1 |L × B | 3|1249| F2 |L × B | 7 | DR × R | 7| 4| 6| 5| 7| 5| 9| 3| 6| 1|..| 4.08| | 78 |732| 703| F1 |M × B | 3|2442| F2 |M × B | 6 | Do. | 1| 3|13|13| 8| 6| 7| 6| 3|..|..| 4.07| | 79 |770| 720| F1 |B × L | 4| 926| F2 | Do. | 3 | DR × DR| 6| 1| 3| 9| 5| 4| 5| 1| 4| 1| 1| 4.05| | 80 |732|2441| F2 |M × B | 0|2442| F2 | Do. | 6 | DR × R |..| 1| 6| 8| 2| 6| 0| 3| 1|..|..| 4.00| | 81 |760|1042| F2 |B × T | 3|1270| F2 |B × T | 2 | DR × DR| 2| 3| 3| 9| 3| 5| 8| 2| 0| 1|..| 4.00| | 82 |731| 384| F1 |L × B | 4|1249| F2 |L × B | 7 | DR × R | 2| 1| 4| 4| 3| 2| 4| 0| 1| 1|..| 3.82| | 83 |814|4566| F2 |B × T | 2|3975| F2 |B × T | 9 | Do. | 1| 4| 2| 4| 3| 2| 1|..|..|..|..| 3.82| | 84 |732| 599| F1 |M × B | 3|2442| F2 |M × B | 6 | Do. | 6| 5|23|10| 5| 3| 4| 5| 8| 3| 1| 3.78| | 85 |770| 761| F1 |B × L | 3| 926| F2 | Do. | 3 | DR × DR| 7| 3| 5| 3| 7| 7| 2| 6| 1| 1|..| 3.71| | 86 |731|1770| F2 | Do. | 7|1249| F2 |L × B | 7 | DR × R | 1|..| 8| 6| 9| 3| 2|..| 2|..|..| 3.65| | 87 |861|5165| F2 |T × C | 10| 95| F1 |T × C | 5 | R × DR |..|..|..|10| 3| 2| 1|..|..|..|..| 3.63| | 88 |754|3175| F2 |B × T | 2| 871| F2 |B × T | 2 | DR × DR| 1|..| 2| 1| 3| 4|..|..|..|..|..| 3.55| | 89 |731|2102| F2 |L × B | 1|1249| F2 |L × B | 7 | DR × R | 1| 0| 4| 2| 4| 1| 1| 1|..|..|..| 3.43| | 90 |840|1755| F2 |M × B | 6|4177| F2 | Do. | 2 | R × DR |..|..| 6| 7| 7| 3| 1|..|..|..|..| 3.42| | 91 |701|2576| F2 |L × B | 2|1898| F2 | Do. | 3 | DR × DR| 2| 1| 1| 8|11| 2| 1|..|..|..|..| 3.35| | 92 |842|2049| F1 | Do. | 3|4385| F2 |M × B | 4 | Do. |11| 1| 2| 8| 5| 3| 1| 0| 2| 2| 2| 3.35| | 93 |754| 853| F2 |B × T | 1| 871| F2 |B × T | 3 | Do. | 2| 3| 4| 6| 4| 1| 6|..|..|..|..| 3.31| | 94 |826|2652| F1 |M × B | 3|4093| F2 |M × B | 0 | Do. | 8| 2| 1| 8| 1|..|..| 1| 2| 3|..| 3.28| | 95 |754|1052| F2 |B × T | 2| 871| F2 |B × T | 2 | Do. | 3|..| 7| 9| 9| 5| 2|..|..|..|..| 3.26| | 96 |701| 965| F2 |T × L × B| 0|1898| F2 |L × B | 3 | Do. | 1| 4| 6|12| 8| 4| 0| 2| 0|..|..| 3.19| | 97 |732|1833| F2 |M × B | 1|2442| F2 |M × B | 6 | DR × R | 1| 1| 7| 6| 6| 4| 1|..|..|..|..| 3.19| | 98 |732| 631| F1 | Do. | 3|2442| F2 | Do. | 6 | Do. | 3| 4|10|16|12| 4| 1| 2|..|..|..| 3.08| | 99 |754| 862| F2 |B × T | 1| 871| F2 |B × T | 2 | DR × DR| 1| 5|10|17|10| 4| 1|..|..|..|..| 2.96| | 100 |837|5641| F2 |T × L × B| 0|4288| F3 |L × B | 2 | Do. | 1| 2| 2| 3|..| 2|..| 1|..|..|..| 2.91| | 101 |840|3841| F2 |L × B | 0|4177| F2 | Do. | 2 | D × DR | 3| 3| 2| 6| 4| 2|..|..|..|..|..| 2.86| | 102 |701| 721| F1 | Do. | 2|1898| F2 | Do. | 3 | DR × DR| 2| 4| 3| 8| 3| 2| 2|..|..|..|..| 2.83| | 103 |839|3949| F2 | Do. | 4|4348| F2 | Do. | 3 | Do. | 1| 2|..|..| 1| 1| 1|..|..|..|..| 2.83| | 104 |840| 732| F1 | Do. | 3|4177| F2 | Do. | 2 | Do. | 7| 6| 9| 8| 7| 2| 1| 2|..| 1|..| 2.67| | 105 |840| 249| F1 | Do. | 3|4177| F2 | Do. | 2 | Do. | 7| 3| 5| 6| 2| 9|..|..|..|..|..| 2.62| | 106 |840|3916| F1.5| Do. | 2|4177| F2 | Do. | 2 | Do. | 5| 1| 4| 2| 2| 2| 1|..|..|..|..| 2.29| | 107 |842|4945| F2 |M,L × B | 1|4385| F2 |M × B | 4 | Do. | 9| 3| 6| 5| 1| 2| 4|..|..|..|..| 2.27| | 108 |731|2595| F2 |L × B | 1|1249| F2 |L × B | 7 | D × R | 6| 6| 7| 1|..|..|..|..|..|..|..| 2.15| | 109 |840|5169| F2 | Do. | 3|4177| F2 | Do. | 2 | DR × DR| 6| 2| 5| 5| 2| 2|..|..|..|..|..| 2.05| | 110 |837|5667| F3 | Do. | 2|4288| F3 | Do. | 2 | Do. | 2| 1| 2|..| 1| 1|..|..|..|..|..| 2.00| | 111 |749|1355| F2 |G × C | 2|1854| F2 |G(C × L)| 0 | DR × D |..| 2| 5| 1|..|..|..|..|..|..|..| 1.87| | 112 |824|3901| F2 |M × S | 1|5095| F2 |M × S | 1 | DR × DR|17| 3| 2| 3|..| 2|..|..| 1| 2|..| 1.73| | 113 |751|1254| F2 |L × B | 0|1139| F2 |L × B | 8 | D × R |17| 5| 5| 4| 3| 3|..| 1|..|..|..| 1.63| | 114 |749| 816| F1 | Do. | 2|1854| F2 |G(C × L)| 0 | DR × D | 6| 7| 3| 5| 1|..|..|..|..|..|..| 1.45| | 115 |749| 929| F2 |G × C | 0|1854| F2 | Do. | 0 | D × D | 8| 3| 1|..|..|..| 1|..|..| 1|..| 1.43| | 116 |749| 819| F1 |L × B | 1|1854| F1.5|G(C × L)| 0 | DR × D | 9| 3| 5| 3|..|..|..|..|..|..|..| 1.10| | 117 |804|5099| F2 |S × Sp | 0|3823| F1 |S × Sp | 0 | D × D | 2|..|..| 1|..|..|..|..|..|..|..| 1.00| | 118 |804|6043| F2 | Do. | 1|3823| F1 | Do. | 0 | Do. |..| 1|..|..|..|..|..|..|..|..|..| 1.00| | 119 |817|5730| F1 |L × Sp | 0|3900| F2 | Do. | 1 | D × DR | 3| 3| 1|..|..|..|..|..|..|..|..| 0.71| | 120 |817|4696| F1 | Do. | 0|3900| F2 | Do. | 1 | Do. | 9| 7| 3|..|..|..|..|..|..|..|..| 0.68| | 121 |817|6046| F2 |S × M | 0|3900| F2 | Do. | 1 | Do. |10|..| 3|..|..|..|..|..|..|..|..| 0.46| | 122 |817|6833| F1.5|L(G × S) | 0|3900| F2 | Do. | 1 | Do. | 6| 2| 1|..|..|..|..|..|..|..|..| 0.44| | 123 |817|5062| F1 |L(Sp) | 0|3900| F2 | Do. | 1 | Do. |18| 7| 2|..|..|..|..|..|..|..|..| 0.41| | 124 |817|5069| F1 | Do. | 0|3900| F2 | Do. | 1 | Do. |21| 7| 2|..|..|..|..|..|..|..|..| 0.37| | 125 |817|6406| F1 | Do. | 0|3900| F2 | Do. | 1 | Do. |25| 8| 2|..|..|..|..|..|..|..|..| 0.34| | 126 |817|7047| F1 | Do. | 0|3900| F2 | Do. | 1 | Do. | 4| 2|..|..|..|..|..|..|..|..|..| 0.33| | 127 |749|2651| F2 |G × C | 0|1854| F2 |G(C × L)| 0 | D × D | 2| 1|..|..|..|..|..|..|..|..|..| 0.33| | 128 |824|4714| F2 |S × Sp | 0|5095| F2 |M × S | 1 | Do. |26| 6| 1| 1|..|..|..|..|..|..|..| 0.32| | 129 |817|4690| F1 | Do. | 0|3900| F2 |S × Sp | 1 | D × DR |21| 6| 1|..|..|..|..|..|..|..|..| 0.29| | 130 |824|7439| F2 | Do. | 0|5095| F2 |M × S | 1 | D × D |11| 4|..|..|..|..|..|..|..|..|..| 0.27| | 131 |804|4715| F2 | Do. | 0|3823| F1 |S × Sp | 0 | DR × DR|18| 2| 1|..|..|..|..|..|..|..|..| 0.19| | 132 |804|3898| F2 |S × M | 0|3823| F1 | Do. | 0 | D × DR |19|..|..|..|..|..|..|..|..|..|..| 0.00| | 133 |804|3902| F2 | Do. | 0|3823| F1 | Do. | 0 | Do. |33|..|..|..|..|..|..|..|..|..|..| 0.00| | 134 |804|4657| F2 | Do. | 0|3823| F1 | Do. | 0 | Do. | 8|..|..|..|..|..|..|..|..|..|..| 0.00| | 135 |804|4716| F2 | Do. | 0|3823| F1 | Do. | 0 | Do. |19|..|..|..|..|..|..|..|..|..|..| 0.00| | 136 |804|5431| F2 | Do. | 0|3823| F1 | Do. | 0 | Do. |16|..|..|..|..|..|..|..|..|..|..| 0.00| +------+---+----+-----+---------+---+----+-----+--------+---+--------+--+--+--+--+--+--+--+--+--+--+--+-----+

In table 38 I have given in the section lying between that headed "Father" and that headed "Offspring" the "Matings." This column differs from the others of the table in not being, in general, based upon observation, but upon a sometimes complicated judgment. Of course, all of the F1 generation, where this generation occurs, may be taken as of DR composition; but the decision as to whether a given individual of F2 is a DR, an extracted dominant, or an extracted recessive is not always easy, because of the manifestation of imperfect dominance. But the assignments are by no means arbitrary. Taking the Brahma crosses, which are by far the most numerous, we see, from tables 31, B and 33, that those F2 individuals that have a boot of grade 6 or higher are almost certainly extracted recessives (which are equivalent to pure-bred Dark Brahmas). Those with a grade of 3 or even 4 and lower to 2 or even 1 are probably heterozygotes, while those with grade 0 and some of those with grade 1 are extracted dominants. In cases of doubt the distribution of grades in the offspring will give the deciding vote. In case the individual has been used as a parent in more than one mating the results in all the matings are taken into account, for the germinal constitution of an individual must be regarded as fixed at all times and in all matings. The assignment under "Matings" has, then, been made by the application of the above rules.

In tables 39 to 43 there are grouped together the progeny from matings of the same sort, selecting from table 38 the crosses into which the Dark Brahma enters as the booted parent.

TABLE 39.--_RR × RR crosses from table 38._

+-------+-----------------------------------------------------+----------------------+ | | Boot-grade in offspring. | Parental grades. | |Serial +--+---+---+---+---+----+----+---+----+----+----+-----+-------+-----+--------+ | No. | 0| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 |Avge.|Female.|Male.|Average.| +-------+--+---+---+---+---+----+----+---+----+----+----+-----+-------+-----+--------+ | 1 |..| ..| ..| ..| ..| ..| ..| ..| ..| 10| 15| 9.6| 7 | 9 | 8.0 | | 2 |..| ..| ..| ..| ..| ..| ..| ..| ..| 1| 1| 9.5| 4 | 8 | 6.0 | | 3 |..| ..| ..| ..| ..| ..| ..| ..| 1| 3| 4| 9.4| 5 | 9 | 7.0 | | 4 |..| ..| ..| ..| ..| ..| ..| ..| 1| 1| 2| 9.3| 6 | 7 | 6.5 | | 5 |..| ..| ..| ..| ..| 1| ..| ..| 3| 4| 9| 9.1| 9 | 9 | 9.0 | | 6 |..| ..| ..| ..| ..| 1| 1| 1| ..| 2| 7| 8.8| 8 | 9 | 8.5 | | 7 |..| ..| ..| ..| ..| ..| 1| 1| 1| 1| 4| 8.8| 2 | 9 | 5.5 | | 8 |..| ..| ..| ..| ..| ..| 1| 1| 2| 2| 3| 8.6| 7 | 5 | 6.0 | | 9 |..| ..| ..| ..| 1| ..| ..| 1| 4| 2| 3| 8.3| 7 | 5 | 6.0 | | 10 |..| ..| ..| ..| ..| ..| 1| 2| 4| 3| ..| 7.9| 8 | 6 | 7.0 | | 11 |..| ..| ..| ..| 1| 1| ..| 3| ..| 6| 1| 7.8| 5 | 5 | 5.0 | | 13 |..| ..| ..| ..| ..| 1| 1| 2| 1| 1| 1| 7.4| 6 | 7 | 6.5 | | 18 |..| ..| ..| ..| 1| ..| 2| ..| 2| ..| 1| 7.0| 10 | 9 | 9.5 | | 21 |..| ..| ..| ..| 3| 7| 7| 7| 7| 5| 2| 6.8| 9 | 6 | 7.5 | | 25 |..| ..| ..| ..| ..| 2| 1| ..| ..| ..| 1| 6.5| 7 | 7 | 7.0 | | 37 |..| ..| ..| 2| 8| 5| 6| 2| 8| 3| ..| 6.0| 8 | 6 | 7.0 | | 39 |..| ..| ..| 5| 4| 6| 6| 1| 11| 1| ..| 5.9| 8 | 8 | 8.0 | | 41 |..| ..| 1| 2| 1| 8| 2| 3| 6| ..| ..| 5.8| 9 | 7 | 8.0 | | 49 |..| 1| 1| 1| 2| 3| ..| 2| 2| 1| ..| 5.2| 10 | 7 | 8.5 | | 55 |..| ..| ..| 2| 1| 4| 1| 2| ..| ..| ..| 5.0| 6 | 7 | 6.5 | | +--+---+---+---+---+----+----+---+----+----+----+-----+ | | | |Totals | | | | | | | | | | | | | | | | | (287)|..| 1| 2| 12| 22| 39| 30| 28| 53| 46| 54| 7.25| | | | |Per | | | | | | | | | | | | | | | | | cent.|..|0.3|0.7|4.2|7.7|13.6|10.5|9.8|18.5|16.0|18.8| ...| | | | +-------+--+---+---+---+---+----+----+---+----+----+----+-----+-------+-----+--------+

TABLE 40.--_DR × RR crosses from table 38._

+-----------+-------------------------------------------------------------+ | | Boot-grade in offspring. | | Serial +---+---+---+----+----+-----+----+----+----+----+----+--------+ | No. | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 |Average.| +-----------+---+---+---+----+----+-----+----+----+----+----+----+--------+ | 14 | ..| 2| 1| ..| 1| 3 | ..| 1 | 3 | 6 | 5 | 7.2 | | 15 | ..| ..| ..| ..| 3| 2 | 3| 1 | 1 | 1 | 5 | 7.1 | | 16 | ..| ..| ..| 1| 4| 1 | 2| 7 | 6 | 1 | .. | 7.1 | | 17 | ..| ..| ..| ..| 1| .. | ..| 1 | .. | .. | 1 | 7.0 | | 20 | ..| ..| ..| 1| 1| 2 | 2| .. | 1 | 1 | 3 | 6.9 | | 22 | ..| ..| ..| 2| 1| .. | 1| .. | .. | 2 | 2 | 6.8 | | 23 | ..| ..| ..| 2| 2| 2 | 1| .. | .. | 3 | 3 | 6.7 | | 24 | ..| ..| ..| ..| 1| .. | ..| 1 | .. | 1 | .. | 6.7 | | 26 | 1| ..| ..| 1| 4| 6 | 9| 4 | 4 | 6 | 3 | 6.5 | | 27 | ..| ..| ..| 2| 3| .. | 3| 1 | 1 | 4 | 1 | 6.5 | | 28 | ..| ..| 1| 2| 6| 13 | 11| 5 | 11 | 8 | 3 | 6.3 | | 29 | ..| ..| ..| 2| 2| 5 | 2| 1 | 1 | 3 | 2 | 6.3 | | 30 | ..| ..| ..| 1| 3| 8 | 5| 2 | .. | 2 | 4 | 6.3 | | 31 | ..| ..| ..| 6| 4| 1 | ..| 1 | 1 | 1 | 6 | 6.2 | | 32 | ..| ..| ..| 1| 5| 4 | 3| 1 | 2 | 2 | 2 | 6.1 | | 33 | ..| ..| ..| 5| 6| 11 | 12| 7 | 4 | 9 | .. | 6.1 | | 34 | ..| ..| 1| ..| ..| .. | 1| .. | 2 | .. | .. | 6.0 | | 35 | ..| ..| 1| ..| ..| 1 | 3| .. | 1 | 1 | .. | 6.0 | | 36 | ..| ..| 2| 3| 3| .. | 2| .. | .. | 5 | 2 | 6.0 | | 40 | ..| 1| 2| 3| 2| 5 | 3| 5 | 9 | 1 | .. | 5.8 | | 42 | ..| ..| 1| 3| 9| 5 | 8| 4 | 7 | 2 | .. | 5.7 | | 43 | ..| ..| ..| ..| 7| 4 | 3| 2 | 3 | 1 | .. | 5.7 | | 44 | ..| ..| ..| 1| ..| 1 | ..| .. | .. | 1 | .. | 5.7 | | 45 | ..| ..| 1| 2| 5| 3 | 1| 1 | 1 | 4 | .. | 5.6 | | 46 | ..| ..| 3| 5| 2| 7 | 5| 6 | 2 | 4 | .. | 5.5 | | 47 | ..| 2| 2| 3| 8| 9 | 5| 3 | 7 | 6 | .. | 5.5 | | 48 | ..| ..| ..| 1| 4| 2 | 1| .. | 1 | .. | 1 | 5.3 | | 51 | ..| ..| ..| ..| 3| 2 | 1| .. | 1 | .. | .. | 5.1 | | 52 | 1| 1| 1| 4| 1| 7 | 2| 2 | 2 | .. | 2 | 5.0 | | 53 | 1| 1| ..| 1| 2| .. | 1| .. | 1 | 1 | 1 | 5.0 | | 54 | ..| ..| ..| 1| 2| 1 | 1| .. | 1 | .. | .. | 5.0 | | 59 | ..| ..| 2| 1| 2| 2 | 1| .. | 1 | .. | .. | 4.9 | | 60 | ..| ..| 2| 19| 8| 13 | 6| 4 | 5 | 2 | 1 | 4.8 | | 61 | ..| 1| 1| 1| 1| .. | 1| .. | 1 | 1 | .. | 4.8 | | 62 | ..| ..| 1| 3| 4| 1 | 1| 2 | .. | 1 | .. | 4.7 | | 63 | 1| 1| 2| 8| 6| 1 | 2| 2 | 4 | 2 | .. | 4.6 | | 66 | ..| ..| ..| 4| 7| 2 | 2| 2 | .. | .. | .. | 4.5 | | 70 | ..| ..| 2| 2| 3| 2 | 2| 1 | .. | .. | .. | 4.3 | | 72 | ..| ..| 1| 9| 6| 6 | 4| 1 | .. | .. | .. | 4.2 | | 73 | ..| ..| 1| ..| 2| 1 | 1| .. | .. | .. | .. | 4.2 | | 77 | 7| 4| 6| 5| 7| 5 | 9| 3 | 6 | 1 | .. | 4.1 | | 78 | 1| 3| 13| 13| 8| 6 | 7| 6 | 3 | .. | .. | 4.1 | | 80 | ..| 1| 6| 8| 2| 6 | ..| 3 | 1 | .. | .. | 4.0 | | 82 | 2| 1| 4| 4| 3| 2 | 4| .. | 1 | 1 | .. | 3.8 | | 83 | 1| 4| 2| 4| 3| 2 | 1| .. | .. | .. | .. | 3.8 | | 84 | 6| 5| 23| 10| 5| 3 | 4| 5 | 8 | 3 | 1 | 3.8 | | 86 | 1| ..| 8| 6| 9| 3 | 2| .. | 2 | .. | .. | 3.7 | | 89 | 1| ..| 4| 2| 4| 1 | 1| 1 | .. | .. | .. | 3.4 | | 90 | ..| ..| 6| 7| 7| 3 | 1| .. | .. | .. | .. | 3.4 | | 97 | 1| 1| 7| 6| 6| 4 | 1| .. | .. | .. | .. | 3.2 | | 98 | 3| 4| 10| 16| 12| 4 | 1| 2 | .. | .. | .. | 3.1 | | +---+---+---+----+----+-----+----+----+----+----+----+--------+ |Total(1199)| 27| 32|117| 181| 200| 172 | 142| 88 |105 | 87 | 48 | 5.04 | |Per cent. |2.3|2.7|9.8|15.1|16.7|14.3 |11.9|7.3 |8.8 |7.2 |4.0 | ... | +-----------+---+---+---+----+----+-----+----+----+----+----+----+--------+

TABLE 41.--_DR × DD crosses._

+---------+------------------------------------------------+ | | Boot-grade in offspring. | | Serial +------+------+------+------+-----+-----+--------+ | No. | 0 | 1 | 2 | 3 | 4 | 5 |Average.| +---------+------+------+------+------+-----+-----+--------+ | 101 | 3 | 3 | 2 | 6 | 4 | 2 | 2.9 | | 113 | 6 | 7 | 3 | 5 | 1 | ... | 1.5 | | 116 | 9 | 3 | 5 | 3 | ... | ... | 1.1 | | +------+------+------+------+-----+-----+--------+ |Total(62)| 18 | 13 | 10 | 14 | 5 | 2 | 1.69 | |Per cent.| 29.5 | 21.3 | 16.4 | 23.0 | 8.2 | 1.6 | ... | +---------+------+------+------+------+-----+-----+--------+

TABLE 42.--_DR x DR crosses._

+-----------+---------------------------------------------------------+ | | Boot-grade in offspring. | |Serial No. +----+---+----+----+----+----+---+---+---+---+---+--------+ | | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10|Average.| +-----------+----+---+----+----+----+----+---+---+---+---+---+--------+ | 19 | ..| ..| ..| ..| 1| 1| ..| ..| ..| 1| ..| 7.0 | | 54 | ..| ..| ..| 2| 1| 6| 4| 2| ..| ..| ..| 5.2 | | 56 | ..| ..| ..| 2| 5| 2| ..| 3| 1| ..| ..| 5.0 | | 57 | ..| 2| 3| 3| 2| 4| 1| 1| 1| 2| 2| 5.0 | | 58 | 1| 2| 1| 4| 1| ..| ..| ..| 8| ..| ..| 4.9 | | 59 | ..| ..| 2| 1| 2| 2| 1| ..| 1| ..| ..| 4.9 | | 64 | ..| ..| ..| ..| 4| 2| 1| ..| ..| ..| ..| 4.6 | | 65 | 1| ..| 3| 6| 1| 4| 2| 7| ..| ..| ..| 4.5 | | 67 | 4| 1| 4| ..| ..| 4| 2| ..| 2| 1| 2| 4.3 | | 68 | 3| 2| 6| 5| 6| 6| 3| ..| 2| 4| 1| 4.3 | | 69 | 9| 3| 1| 6| 8| 2| 6| 6| 3| 1| 3| 4.3 | | 71 | ..| ..| 2| 2| 3| 2| 2| 1| ..| ..| ..| 4.3 | | 75 | ..| 2| 5| 11| 7| 10| 5| ..| 2| 1| ..| 4.1 | | 76 | 3| 2| 1| 9| 5| 5| 2| 2| 3| 1| ..| 4.1 | | 79 | 6| 1| 3| 9| 5| 4| 5| 1| 4| 1| 1| 4.1 | | 81 | 2| 3| 3| 9| 3| 5| 8| 2| ..| 1| ..| 4.0 | | 85 | 7| 3| 5| 3| 7| 7| 2| 6| 1| 1| ..| 3.7 | | 88 | 1| ..| 2| 1| 3| 4| ..| ..| ..| ..| ..| 3.6 | | 91 | 2| 1| 1| 8| 11| 2| 1| ..| ..| ..| ..| 3.4 | | 92 | 11| 1| 2| 8| 5| 3| 1| ..| 2| 2| 2| 3.4 | | 93 | 2| 3| 4| 6| 4| 1| 6| ..| ..| ..| ..| 3.3 | | 94 | 8| 2| 1| 8| 1| ..| ..| 1| 2| 3| ..| 3.3 | | 95 | 3| ..| 7| 9| 5| 2| ..| ..| ..| ..| ..| 3.3 | | 96 | 1| 4| 6| 12| 8| 4| ..| 2| ..| ..| ..| 3.2 | | 99 | 1| 5| 10| 17| 10| 4| 1| ..| ..| ..| ..| 3.0 | | 100 | 1| 2| 2| 3| ..| 2| ..| 1| ..| ..| ..| 2.9 | | 102 | 2| 4| 3| 8| 3| 2| 2| ..| ..| ..| ..| 2.8 | | 103 | 1| 2| ..| ..| 1| 1| 1| ..| ..| ..| ..| 2.8 | | 104 | 7| 6| 9| 8| 7| 2| 1| 2| ..| 1| ..| 2.7 | | 105 | 7| 3| 5| 6| 2| 9| ..| ..| ..| ..| ..| 2.6 | | 106 | 5| 1| 4| 2| 2| 2| 1| ..| ..| ..| ..| 2.3 | | 107 | 9| 3| 6| 5| 1| 2| 4| ..| ..| ..| ..| 2.3 | | 109 | 6| 2| 5| 5| 2| 2| ..| ..| ..| ..| ..| 2.1 | | 110 | 2| 1| 2| ..| 1| 1| ..| ..| ..| ..| ..| 2.0 | | +----+---+----+----+----+----+---+---+---+---+---+--------+ |Total (851)| 105| 61| 108| 178| 127| 109| 62| 37| 32| 20| 12| 3.59 | |Per cent. |12.3|7.2|12.7|20.9|14.9|12.8|7.3|4.4|3.8|2.3|1.4| ... | +-----------+----+---+----+----+----+----+---+---+---+---+---+--------+

TABLE 43.--_DD x DD (Silkie crosses)._

+-----------+----------------------------+ | | Boot-grade in offspring. | |Serial No. +----+----+----+----+--------+ | | 0 | 1 | 2 | 3 |Average.| +-----------+----+----+----+----+--------+ | 117 | 2| ..| ..| 1| 1.00 | | 118 | ..| 1| ..| ..| 1.00 | | 128 | 26| 6| 1| 1| 0.32 | | 130 | 11| 4| ..| ..| 0.27 | | 131 | 18| 2| 1| ..| 0.19 | | 132 | 19| ..| ..| ..| 0.0 | | 133 | 33| ..| ..| ..| 0.0 | | 134 | 8| ..| ..| ..| 0.0 | | 135 | 19| ..| ..| ..| 0.0 | | 136 | 16| ..| ..| ..| 0.0 | | +----+----+----+----+--------+ |Total (169)| 152| 13| 2| 2| 0.14 | |Per cent. |89.9| 7.7| 1.2| 1.2| .... | +-----------+----+----+----+----+--------+

The significance of the data given in tables 39 to 43 is best brought out by summarizing them. Especially instructive is a comparison of the pure-bred with the hybrids. Since the data are most complete in the case of the Brahma crosses, these will be considered in most detail. So far as they go, the results with the Cochins and Silkies are entirely confirmatory.

Table 44 shows clearly, first, that there are families of two booted parents that never fail to produce booted offspring. There is, however, even in pure-bred booted races, a marked variability in the grade of booting, extending from 3 (or 4) to 10. The significance of this variability must be left for future investigations. There is in the least boot, as it were, an extension of the field of activity of the feather-inhibiting factor that is always present on the hinder aspect of the shank, so that it interferes with the development of feathers on the inner face of the shank also.

In the first hybrid generation all somatic cells are hybrid. The feather inhibitor is present in the skin of the shank, but its strength is diluted by the presence in the same cells of a protoplasm devoid of the inhibiting property. Consequently, the prevailing grade of the boot falls from 6 (or 10) to 3. Despite the dilution, inhibition is complete in about 8 per cent of the offspring (grade 0); in about 10 per cent of the offspring the inhibiting factor is so weak that the boot develops as in the pure-blooded Brahma. When, as a result of inbreeding F1's, the feather-inhibiting factor is eliminated from certain offspring, and such full-feathered birds are bred together, we find a return of the mode to high numbers, such as 8 to 10 (but also 5). There is no doubt of segregation.

TABLE 44.--_Brahma crosses. (All entries are percentages.)_

+---------------+------+----------------------------------------------------------------------------+ | | | Boot-grade in offspring. | | Percentage. | From +------+------+-----+-----+-----+-----+-----+-----+-----+-----+-----+--------+ | |table.| | | | | | | | | | | |Average | | | | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | grade. | +---------------+------+------+------+-----+-----+-----+-----+-----+-----+-----+-----+-----+--------+ |Pure blood | 31, B| .... | .... | ....| 3.3| 3.3| 6.6| 24.6| 4.9| 9.8| 14.8| 32.8| 7.62 | |F1 (D × R) | 32 | 7.9 | 13.8 | 16.8| 31.0| 17.5| 7.8| 3.4| 1.1| 0.7| ....| ....| 2.84 | |Extracted R × R| 39 | .... | 0.3 | 0.7| 4.2| 7.7| 13.6| 10.5| 9.8| 18.5| 16.0| 18.8| 7.25 | |DR × RR | 40 | 2.3 | 2.7 | 9.8| 15.1| 16.7| 14.3| 11.9| 7.3| 8.8| 7.2| 4.0| 5.04 | | | |\---------------\/---------------/ \--------------\/-------------/| | | | | 50 p. ct. DR. 50 p. ct. RR. | | |DR × DR | 42 | 12.3 | 7.2 | 12.7| 20.9| 14.9| 12.8| 7.3| 4.4| 3.8| 2.3| 1.4| 3.59 | | | |\------\/------/ \------\/------/ \--------------\/-------------/| | | | | 25 p. ct. DD. 50 p. ct. DR. 25 p. ct. RR. | | |DR × DD | 41 | 29.5 | 21.3 | 16.4| 23.0| 8.2| 1.6| ....| ....| ....| ....| ....| 1.69 | | | |\-----\/----/|\----------\/---------/| | | | | | | | | |50 p. ct. DD.| 50 p. ct. DR. | | | | | | | +---------------+------+-------------+-----------------------+-----+-----+-----+-----+-----+--------+

If a heterozygous bird be mated to a recessive the variability of the offspring is much increased, owing to the occurrence in the progeny of both DR and RR individuals (table 40). The offspring do not, to be sure, fall into two distinct and well-defined types, as in typical Mendelian cases; but one part of the range of variation agrees fairly with that of pure RR's, _i. e._, Brahmas, and the remainder with that of heterozygotes. And if we make the division in the middle of the middle class, viz, 5, we shall find a close approximation to that equality of extracted recessives and heterozygotes that the segregation theory calls for (table 44).

If, again, two heterozygous birds be mated, the variability is still greater and the proportion of clean-footed offspring rises to 12 per cent. These, together with some of the extremely slightly booted offspring, represent the extracted dominants. The whole range now falls into three regions divided by the middle of grades 2 and 5. These regions correspond to the DD's, the DR's, and the RR's of typical cases of segregation, and their relative proportions are approximately as 25: 50: 25.

Finally, if a heterozygote be mated to an extracted dominant the proportion of clean-footed offspring rises to about 30 per cent and the whole range of variation falls readily into two parts, the one comprising grades 0 and 1, the other grades 2 and above. The first includes the DD offspring; the second, the DR's; and their frequency is equal. One will not fail to note that we are not here dealing with a case of blending simply, and the inheritance of the blend; such a view is negatived by the fact of the much greater variability of DR × DR cross over the simple D × R cross of the first generation. One may safely conclude, then, that, despite the apparent blending of booting characters in the first generation of hybrids, true segregation takes place. But this is always to be seen through the veil of imperfect dominance.

A casual examination of table 38 would seem to show a correlation between the grade of booting of the parents and that of the average of their progeny. Thus, on the whole, the parental grades run high in the upper part of the table and run low in the lower part. This relation would thus seem to confirm Castle's conclusion for polydactylism in guinea-pigs that there is an inheritance of the degree of a character. One consequence of such an inheritance would be that it would be possible in a few generations to increase or diminish the grade of a character and fix any required grade in the germ-plasm. A more careful consideration of the facts of the case shows that this relation has another interpretation. The grade of boot of the different parents varies largely because their gametic constitution is diverse. As table 39 shows, the parents of the upper part of table 38 are chiefly extracted recessives, and consequently their booting and that of their offspring are characterized by high grades. On the other hand, the parents of the lower part of the table are heterozygous or extracted dominants and, consequently, their grades and also those of their offspring average low. On account of the lack of homogeneity of the families in table 38, one can draw from it no proper conclusions as to relation between parental and filial grades. On the other hand, from a homogeneous table, like table 39, we can hope to reach a conclusion as to the existence of such a relation. I have calculated, in the usual biometric fashion, the coefficient of correlation between average parental and filial grades, and found it to be -0.17 ± 0.13. This can only be interpreted to mean that in a homogeneous assemblage of families there is no correlation between the grade of booting of parents and offspring.