A new series of four-associate class partially balanced incomplete block designs in two replications has been proposed. The blocks of these designs are of two different sizes. The blocks can be divided into two groups such that every treatment appears in each group exactly once, and any two blocks belonging to two different groups have a constant number of treatments in common, i.e., these designs are affine resolvable.
Partially balanced incomplete block (PBIB) designs form an important class of block designs. If the experimenter is constrained of resources, PBIB designs with higher associate classes in minimum replications are an alternative to the more popular class of block designs, i.e., balanced incomplete block (BIB) designs or two-associate class PBIB designs. Furthermore, it is advisable to opt for a resolvable block design for situations where experimentation is to be done, one complete replication at one location/season, considering spatial/temporal variations. Some distinguished classes of resolvable PBIB designs are available in the literature (Rao [3]; Williams et al. [5]; Kageyama [2]; Varghese and Sharma [4]; Agrawal et al. [1]). Again, equally sized blocks may not always be feasible in every experimental situation. Hence, it might be of interest to the experimenters to have resolvable PBIB designs in fewer replications with unequal block sizes.
We define a new association scheme in Section 2. A general method of constructing resolvable PBIB designs in unequal block sizes based on this association scheme is given in Section 3. In Section 4, an outline of the analysis of these designs is given.
Let the number of treatments be v =
2mt(t-1) where, m
For any given treatment
Groups | Rows | Columns: Set 1 | Columns: Set 2 | ||||||
1 | 1 | 2 |
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Rows | Columns 1 | Columns 2 | |||
A | B | C | D | ||
1 | 1 | 1 | 2 | 9 | 10 |
2 | 3 | 4 | 11 | 12 | |
3 | 5 | 6 | 13 | 14 | |
4 | 7 | 8 | 15 | 16 | |
2 | 1 | 17 | 18 | 25 | 26 |
2 | 19 | 20 | 27 | 28 | |
3 | 21 | 22 | 29 | 30 | |
4 | 23 | 24 | 31 | 32 | |
3 | 1 | 33 | 34 | 41 | 42 |
2 | 35 | 36 | 43 | 44 | |
3 | 37 | 38 | 45 | 46 | |
4 | 39 | 40 | 47 | 48 |
Different associates of selected treatments, say, treatment 1, 20 and 40, are listed in Table 3.
Treatments | First Associates | Second Associates | Third Associates | Fourth Associates |
1 | 2,9,10 | 3,4,5,6,7,8,11, 12,13,14,15,16 | 17,18,25,26,33,34,41,42 | 19,20,21,22,23,24,27,28,29,30,31,32,35,36, 37,38,39,40,41,42,43,44,45,46,47,48 |
20 | 19,27,28 | 17,18,21,22,23,24,25,26,29,30,31,32 | 3,4,11,12,35,36,43,44 | 1,2,5,6,7,8,9,10,13,14,15,16,33,34,37,38,39,40,41,42,45, 46,47,48 |
40 | 39,47,48 | 33,34,35,36,37,38,41,42,43,44,45,46 | 7,8,15,16,23,24,31,32 | 1,2,3,4,5,6,9,10,11,12,13,14,17,18,19,20,21,22,25,26,27, 28,29,30 |
The method of construction is summarized below:
The first b
Here, the blocks of the design can be divided into two groups such
that in each group, every treatment appears precisely once, and any two
blocks belonging to two different groups have
It has been verified that all the parametric relationships of the
association scheme and designs are satisfied for the above class of
designs.
Replications | Blocks | Treatments | |||||||||||||||
I | i | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 |
ii | 17 | 18 | 19 | 20 | 21 | 22 | 23 | 24 | 25 | 26 | 27 | 28 | 29 | 30 | 31 | 32 | |
iii | 33 | 34 | 35 | 36 | 37 | 38 | 39 | 40 | 41 | 42 | 43 | 44 | 45 | 46 | 47 | 48 | |
II | iv | 1 | 2 | 9 | 10 | 17 | 18 | 25 | 26 | 33 | 34 | 41 | 42 | ||||
v | 3 | 4 | 11 | 12 | 19 | 20 | 27 | 28 | 35 | 36 | 43 | 44 | |||||
vi | 5 | 6 | 13 | 14 | 21 | 22 | 29 | 30 | 37 | 38 | 45 | 46 | |||||
vii | 7 | 8 | 15 | 16 | 23 | 24 | 31 | 32 | 39 | 40 | 47 | 48 |
The analysis of these designs may be carried out using the same
approach as PBIB designs. However, as the proposed designs are
resolvable, the following nested model is appropriate for a set-up of
v treatments in b (=2t-1) blocks where
t-1 blocks are of size 2mt and t blocks are
of size 2m(t-1):
Here,
Solving the normal equations, obtained by minimizing the residual sum of squares, will lead to the following general expressions for variances of elementary contrasts between two estimated treatment effects:
The average variance of elementary contrasts between two estimated
treatment effects is then calculated as:
The first author is thankful to the P.G. School, ICAR-IARI for the financial assistance. The authors are grateful to the editor and reviewers for their valuable comments that helped improve our manuscript’s quality.
1970-2025 CP (Manitoba, Canada) unless otherwise stated.