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RA 00110.pdf - OAR@ICRISAT

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Table 3. Two analyses of variance showing that the location * entry interaction is the appropriate test either with or<br />

without replication at each location<br />

Analysis of Variance I<br />

Source<br />

Locations<br />

Entries<br />

L x E<br />

df<br />

l-1<br />

e-1<br />

(l-1)(e-1)<br />

E.M.S.<br />

Source<br />

Locations<br />

Replications in Locations<br />

Entries<br />

L x E<br />

Error<br />

Analysis of Variance II<br />

df<br />

l-1<br />

/(r-1)<br />

e-1<br />

(l-l)(e-1)<br />

/(r-1)(e-1)<br />

E.M.S.<br />

ments may be sampled with a given number of replications<br />

rather than precisely evaluating each entry in<br />

a smaller number of environments.<br />

Blocking<br />

In testing families, the breeder usually is faced with<br />

experiments containing many entries. Blocking is<br />

required in order to remove environmental variation<br />

arising from differences in the field from one part of<br />

a replication to another. Lattices work well but a<br />

simpler approach is to use incomplete blocks. For<br />

example, a test of 100 entries could be divided into<br />

10 incomplete blocks of 10 entries each. Each<br />

incomplete block will contain the same entries in all<br />

replications. In a blocks-in-replication design, the<br />

blocks are randomized in each replication. In a<br />

replication-in-blocks design all the replications of a<br />

block containing the same entries are grown together<br />

in the block to minimize the error term. The blocksin-replication<br />

design is somewhat better from a<br />

selection point of view, and is also adaptable to<br />

testing entries with one replication in each location<br />

since locations can be substituted for replications.<br />

However, the replication-in-blocks is slightly favored<br />

for estimating genetic variances. Analyses of variance<br />

and further discussion of these designs are<br />

found in Ross and Gardner (1985). Whatever the<br />

type of experimental design used, some sort of<br />

blocking is almost always required.<br />

When making selections there are two ways to<br />

handle the blocks. One way is to calculate the mean<br />

of each block and the overall mean, and then adjust<br />

the entries in the block by the deviation of the block<br />

mean from the overall mean. The other way to make<br />

selections is to select equally from each block. Both<br />

systems work well, but care is necessary not to have<br />

the blocks too small. The fraction (where e is<br />

the number of entries per block) of the genetic variance<br />

will go into block-to-block variance and be<br />

lost. If e is large enough (say 10 or more) this fraction<br />

may not be sufficiently large to cause worry. Blocks<br />

that are too large (say 50 or more), however, may not<br />

remove enough of the environmental variance.<br />

Improving Populations or Varieties<br />

and their Crosses<br />

Intrapopulation (Variety) Improvement<br />

Methods most usually seen are mass, half-sib,<br />

including ear-to-row, full-sib, and line per se selection,<br />

or some combination of these.<br />

In the prediction equations for each method<br />

(Table 4a, b, c, d), some common terms are used so<br />

the schemes can be compared with each other.<br />

N e = effective population size<br />

= gain per cycle<br />

k = selection coefficient based on proportion selected<br />

= total genetic variation<br />

= additive genetic variance<br />

= dominance genetic variance<br />

111

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