TABLE 1. Expectations for genetic effects in a
diallel crossbreeeding system
Breed of sire (j) |
Breed of
dam (i) |
||
A |
B |
C |
|
A |
|
|
|
|
|
|
|
0 |
|
|
|
B |
|
|
|
|
|
|
|
|
0 |
|
|
C |
|
|
|
|
|
|
|
|
|
0 |
where:
and
are breed
average individual and maternal effects, and
, is the mean heterosis effect for a two-breed reciprocal
cross
, is mean phenotype for one purebred
Xij, is mean
phenotype for a two-breed-cross
breed maternal less
paternal effect, because
breed mean individual
effect
mean heterosis for
reciprocal cross.
specific reciprocal
effect
breed mean heterosis
Table 2. Second phase of diallel mating design to estimate heterosis for maternal effects on progeny performance (hM)a.
Breed of dams |
Breed of
sires |
|||
A |
B |
C |
D |
|
A |
|
B•A |
C•A |
D•A |
B |
A•B |
|
C•B |
D•B |
C |
A•C |
B•C |
|
D•C |
D |
A•D |
B•D |
C•D |
|
AB+BA |
|
|
C(AB+BA) |
D(AB+BA) |
AC+CA |
|
B(AC+CA) |
|
D(AC+CA) |
AD+DA |
|
B(AD+DA) |
C(AD+DA) |
|
BC+CB |
A(BC+CB) |
|
|
D(BC+CB) |
BD+DB |
A(BD+DB) |
|
C(BD+DB) |
|
CD+DC |
A(CD+DC) |
B(CD+DC) |
|
|
|
aSampling
error for estimates of will be minimum, for
any total scale of experiment, when equal
numbers of contemporary progeny are produced for each mating combination,
i.e. DA, DB, D(A•B) and D(B•A), and when each sire of a breed produces the same
proportion of progeny in each cross.
Table 3.
Expected fraction of defined genetic components in deviations of alternative
crossbreeding categories from weighted
mean of parental breeds relative to
Ft
heterosis, h = d + l/2gg.
generationa |
Heterosis |
|
|
Recombinationb |
|
|
|
||||
|
|
|
|
|
|
|
|
|
|
|
|
|
1 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
|
1/2 |
1 |
1 |
1/4 |
1/2 |
0 |
0 |
0 |
0 |
0 |
0 |
A(A●B)
AB×A AB×B Composite |
1/2 |
1/2 |
1/2 |
1/4 |
1/2 |
1/4 |
1/2 |
1/4 |
1/2 |
0 |
0 |
1/2 |
1 |
0 |
|
|
|
|
|
|
|
|
|
SCALESYM32} |
1/8 |
1/2 |
0 |
0 |
0 |
0 |
0 |
0 |
|||
1/2 |
0 |
1 |
|
|
|
|
|
|
|
|
|
|
––– |
> |
|
|
|
|
|
|
|
|
|
n=2 |
1/2 |
1/2 |
1/2 |
1/4 |
1/2 |
1/4 |
1/2 |
1/4 |
1/2 |
0 |
0 |
n=3 |
2/3 |
2/3 |
2/3 |
1/3 |
2/3 |
1/3 |
2/3 |
1/3 |
2/3 |
0 |
0 |
n=4 |
3/4 |
3/4 |
3/4 |
3/8 |
3/4 |
3/8 |
3/4 |
3/8 |
3/4 |
0 |
0 |
Rotation |
|
–––> |
0 |
|
|
|
|
0 |
0 |
|
|
n=2 |
2/3 |
–––> |
0 |
1/9 |
4/9 |
1/9 |
4/9 |
0 |
0 |
0 |
0 |
n=3 |
6/7 |
–––> |
0 |
1/7 |
4/7 |
1/7 |
4/7 |
0 |
0 |
0 |
0 |
n=4 |
14/15 |
–––> |
0 |
7/45 |
28/45 |
7/45 |
28/45 |
0 |
0 |
0 |
0 |
C♂ Rotation♀ |
|
|
|
|
|
|
|
|
|
|
|
n=2 |
1 |
2/3 |
0 |
1/9 |
4/9 |
1/9 |
4/9 |
0 |
0 |
0 |
0 |
n=3 |
1 |
6/7 |
0 |
1/7 |
4/7 |
1/7 |
4/7 |
0 |
0 |
0 |
0 |
n=4 |
1 |
14/15 |
0 |
1/45 |
28/45 |
7/45 |
28/45 |
0 |
0 |
0 |
0 |
3-breed Cross |
|
|
|
|
|
|
|
|
|
|
|
C♂ × A ● B♀ |
1 |
1 |
0 |
1/8 |
1/4 |
0 |
0 |
0 |
|
|
|
a ● b♂ × C♀ |
1 |
0 |
1 |
1/8 |
1/4 |
0 |
0 |
0 |
|
|
|
4 Breed Cross CD♂ × AB♀ |
|
|
|
|
|
|
|
|
|
|
|
1 |
1 |
1 |
1/4 |
1/2 |
0 |
0 |
0 |
|
|
aMean of reciprocal
crosses, equilibrium for n sire breed rotation, or for qi,
fractions of n breeds in a composite at F3 or later
generation.
bFrom Dickerson
(1973) and Hill (1982).
Table 4.
Expected fraction of defined genetic components in linear contrasts between
means for alternative matinga
Code |
Linear
Contrast |
|
|
|
|
|
|
1 |
BA–AA |
(B–A)/2 |
BA |
0 |
0 |
0 |
0 |
2 |
BA–CA |
(B–C)/2 |
BA–CA |
0 |
0 |
0 |
0 |
3 |
A(BA)–AA |
(B–A)/4 |
BA/2 |
BA/8 |
(B–A)/2 |
BA |
0 |
4 |
(BA)2–AA |
(B–A)/2 |
BA/2 |
BA/4 |
(B–A)/2 |
BA |
0 |
5 |
B(BA)–AA |
3(B–A)/4 |
BA/2 |
BA/8 |
(B–A)/2 |
BA |
0 |
5–3 |
|
(B–A)/2 |
0 |
0 |
0 |
0 |
0 |
4–(3+5)/2 |
|
0 |
0 |
BA/8 |
0 |
0 |
0 |
6 |
A(BA)–A(CA) |
(B–C)/4 |
(BA–CA)/2 |
(BA–CA)/8 |
(B–C)/2 |
BA–CA |
0 |
7 |
(BA)2–(CA)2 |
(B–C)/2 |
(BA–CA)/2 |
(BA–CA)/4 |
(B–C)/2 |
BA–CA |
0 |
8 |
B(BA)–C(CA) |
3(B–C)/4 |
(BA–CA)/2 |
(BA–CA)/8 |
(B–C)/2 |
BA–CA |
0 |
8–6 |
|
(B–C)/2 |
0 |
0 |
0 |
0 |
0 |
7–(8+6)/2 |
|
0 |
0 |
(BA–CA)/8 |
0 |
0 |
0 |
9 |
D(BA)–AA |
|
(DB+DA)/2 |
BA/8 |
(B–A)/2 |
BA |
0 |
10 |
D(A·BA)–AA |
|
|
3BA/32 |
(B–A)/4 |
BA/2 |
BA/8 |
11 |
D(BA)2–AA |
|
(DB+DA)/2 |
4BA/32 |
(B–A)/2 |
BA/2 |
BA/4 |
12 |
D(B·BA)–AA |
|
|
3BA/32 |
3(B–A)/4 |
BA/2 |
BA/8 |
12–10 |
|
(B–A)/4 |
(DB–DA)/2 |
0 |
(B–A)/2 |
0 |
0 |
9–11 |
|
0 |
0 |
0 |
0 |
BA/2 |
–BA/4 |
13 |
D(BA–D(CA) |
(B–C)/4 |
(DB–DC)/2 |
(BA–CA)/8 |
(B–C)/2 |
BA–CA |
0 |
14 |
D(A·BA)–D(A·CA) |
(B–C)/8 |
(DB–DC)/4 |
3(BA–CA)/32 |
(B–C)/4 |
(BA–CA)/2 |
(BA–CA)/8 |
15 |
D(BA)2 –D(CA)2 |
(B–C)/4 |
(DB–DC)/2 |
(BA–CA)/8 |
(B–C)/2 |
(BA–CA)/2 |
(BA–CA)/4 |
16 |
D(B·BA)–D(C·CA) |
3(B–C)/8 |
3(DB–DC)/4 |
3(BA–CA)/32 |
(B–C)/4 |
(BA–CA)/2 |
(BA–CA)/8 |
13–15 |
|
0 |
0 |
0 |
0 |
(BA–CA)/2 |
–(BA–CA)/4 |
15–(14+16)/2 |
|
|
|
|
|
|
|
11–(10+12)/2 |
0 |
0 |
(BA–CA)/32 |
0 |
0 |
(BA–CA)/8 |
a"Individual
(I) and maternal (M) additive (gI and gM), heterosis hI
and hM and non-allelic gene interaction (rI and rM)
effects on performance traits.
Table 5. Level of significance (P) for a 5% mean difference (+ or -) between two strains in traits with differing Coefficient Variation (CV) and heritability (h2).
No progeny
per |
No. sires
/strain Ns |
SEa |
t = |
Minimum t
forc |
|||
strain |
sire |
P05 |
P01 |
||||
a. CV = 20%; h2 = 10% |
|
|
|
|
|||
280 |
28 |
|
10 |
1.95 |
2.57 |
2.10 |
2.88 |
|
20 |
|
14 |
1.87 |
2.67 |
2.06 |
2.78 |
|
14 |
|
20 |
1.81 |
2.76 |
2.02 |
2.71 |
|
10 |
|
28 |
1.77 |
2.82 |
2.01 |
2.67 |
|
5 |
|
56 |
1.72 |
2.90 |
1.98 |
2.62 |
220 |
20 |
|
11 |
2.11 |
2.37 |
2.09 |
2.85 |
|
10 |
|
22 |
2.00 |
2.50 |
2.02 |
2.71 |
|
5 |
|
44 |
1.94 |
2.57 |
1.99 |
2.63 |
b. CV = 10%; h2 = 10% |
|
|
|
|
|||
140 |
20 |
|
7 |
1.45 |
3.44 |
2.18 |
3.06 |
|
10 |
|
14 |
1.32 |
3.78 |
2.06 |
2.78 |
|
5 |
|
28 |
1.25 |
3.99 |
2.01 |
2.67 |
100 |
20 |
|
5 |
1.72 |
2.91 |
2.31 |
3.36 |
|
10 |
|
10 |
1.56 |
3.20 |
2.10 |
2.88 |
|
5 |
|
20 |
1.48 |
3.37 |
2.02 |
2.71 |
80 |
20 |
|
4 |
1.92 |
2.60 |
2.45 |
3.71 |
|
10 |
|
8 |
1.75 |
2.85 |
2.14 |
2.98 |
|
5 |
|
16 |
1.66 |
3.02 |
2.04 |
2.75 |
60 |
20 |
|
3 |
2.22 |
2.25 |
2.78 |
4.60 |
|
10 |
|
6 |
2.02 |
2.47 |
2.23 |
3.17 |
|
5 |
|
12 |
1.92 |
2.60 |
2.07 |
2.82 |
40 |
20 |
|
2 |
2.72 |
1.84 |
4.30 |
9.92 |
|
10 |
|
4 |
2.48 |
2.02 |
2.45 |
3.71 |
|
5 |
|
8 |
2.34 |
2.13 |
2.14 |
2.98 |
with
Total phenotypic
variance are expressed as the squared coefficient of variation (%), assuming
one (1) progeny per dam.
cSee Table A.3
in Steele and Torrie (1960) or any other source of probability values for t-ratio, plus or minus mean difference (i.e.
2-tailed distributions).
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Animal breeding: selected articles
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Small ruminants in the Near East -
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21 |
Guideline for dairy accounting,
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55 |
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Recursos
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56 |
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Disease control in semen and
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Animal genetic resources -
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Utilization of renewable energy
sources and energy saving technologies by small scale milk plants and
collection centres, 1992 (E) |
|||||||
94 |
Proceedings of the FAO expert
consultation on the genetic aspects of trypanotolerance, 1992 (E) |
|||||||
95 |
Roots, tubers, plantains and
bananas in animal feeding, 1992 (E) |
|||||||
96 |
Distribution and impact of
helminth diseases of livestock in developing countries, 1992 (E) |
|||||||
97 |
Construction and operation of
medium-sized abattoirs in developing countries, 1992 (E) |
|||||||
98 |
Small scale poultry processing,
1992 (E) |
|||||||
99 |
In situ conservation
of livestock and poultry, 1992 (E) |