Like a randomized complete block design (RCBD), a GRBD is randomized. Within each block, treatments are randomly assignedtoexperimental units: this randomization is also independent between blocks. In a (classic) RCBD, however, there is no replication of treatments within blocks.[2]
The experimental design guides the formulation of an appropriate linear model. Without replication, the (classic) RCBD has a two-way linear-model with treatment- and block-effects but without a block-treatment interaction. Without replicates, this two-way linear-model that may be estimated and tested without making parametric assumptions (by using the randomization distribution, without using a normal distribution for the error).[3] In the RCBD, the block-treatment interaction cannot be estimated using the randomization distribution; a fortiori there exists no "valid" (i.e. randomization-based) test for the block-treatment interaction in the analysis of variance (anova) of the RCBD.[4]
The distinction between RCBDs and GRBDs has been ignored by some authors, and the ignorance regarding the GRCBD has been criticized by statisticians like Oscar Kempthorne and Sidney Addelman.[5] The GRBD has the advantage that replication allows block-treatment interaction to be studied.[6]
GRBDs when block-treatment interaction lacks interest[edit]
However, if block-treatment interaction is known to be negligible, then the experimental protocol may specify that the interaction terms be assumed to be zero and that their degrees of freedom be used for the error term.[7] GRBD designs for models without interaction terms offer more degrees of freedom for testing treatment-effects than do RCBs with more blocks: An experimenter wanting to increase power may use a GRBD rather than RCB with additional blocks, when extra blocks-effects would lack genuine interest.
The GRBD has a real-number response. For vector responses, multivariate analysis considers similar two-way models with main effects and with interactions or errors. Without replicates, error terms are confounded with interaction, and only error is estimated. With replicates, interaction can be tested with the multivariate analysis of variance and coefficients in the linear model can be estimated without bias and with minimum variance (by using the least-squares method).[8][9]
Functional models for block-treatment interactions: Testing known forms of interaction[edit]
Non-replicated experiments are used by knowledgeable experimentalists when replications have prohibitive costs. When the block-design lacks replicates, interactions have been modeled. For example, Tukey's F-test for interaction (non-additivity) has been motivated by the multiplicative model of Mandel (1961); this model assumes that all treatment-block interactions are proportion to the product of the mean treatment-effect and the mean block-effect, where the proportionality constant is identical for all treatment-block combinations. Tukey's test is valid when Mandel's multiplicative model holds and when the errors independently follow a normal distribution.
Tukey's F-statistic for testing interaction has a distribution based on the randomized assignment of treatments to experimental units. When Mandel's multiplicative model holds, the F-statistics randomization distribution is closely approximated by the distribution of the F-statistic assuming a normal distribution for the error, according to the 1975 paper of Robinson.[10]
The rejection of multiplicative interaction need not imply the rejection of non-multiplicative interaction, because there are many forms of interaction.[11][12]
Generalizing earlier models for Tukey's test are the “bundle-of-straight lines” model of Mandel (1959)[13] and the functional model of Milliken and Graybill (1970), which assumes that the interaction is a known function of the block and treatment main-effects. Other methods and heuristics for block-treatment interaction in unreplicated studies are surveyed in the monograph Milliken & Johnson (1989).
A more detailed treatment occurs in Chapter 9.7 in Hinkelmann and Kempthorne. (Hinkelmann and Kempthorne do discuss block-treatment interaction for more complicated blocking structures, like crossed-blocking factors in Chapter 9.6, and for forms of "non-additivity" that may be removed by transformations).
If the scientists do not know that the block-treatment interaction is zero, Addelman requires that the generalized randomized block design be used, because otherwise the block-treatment interaction and the error are confounded. In this situation, where scientists are uncertain whether the block-treatment interaction is zero, Hinkelmann and Kempthorne recommend that the generalized randomized block design be used "if at all possible" (page 312).
^Johnson & Wichern (2002, p. 312, “Multivariate two-way fixed-effects model with interaction”, in “6.6 Two-way multivariate analysis of variance”, p. 307–317)
Addelman, Sidney (Oct 1969). "The Generalized Randomized Block Design". The American Statistician. 23 (4): 35–36. doi:10.2307/2681737. JSTOR2681737.
Addelman, Sidney (Sep 1970). "Variability of Treatments and Experimental Units in the Design and Analysis of Experiments". Journal of the American Statistical Association. 65 (331): 1095–1108. doi:10.2307/2284277. JSTOR2284277.
Gates, Charles E. (Nov 1995). "What Really Is Experimental Error in Block Designs?". The American Statistician. 49 (4): 362–363. doi:10.2307/2684574. JSTOR2684574.
Lentner, Marvin; Bishop, Thomas (1993). "The Generalized RCB Design (Chapter 6.13)". Experimental design and analysis (Second ed.). Blacksburg, VA: Valley Book Company. pp. 225–226. ISBN0-9616255-2-X.
Mardia, K. V.; Kent, J. T.; Bibby, J. M. (1979). "12 Multivariate analysis of variance". Multivariate analysis. Academic Press. ISBN0-12-471250-9.
Milliken, George A.; Johnson, Dallas E. (1989). Nonreplicated experiments: Designed experiments. Analysis of messy data. Vol. 2. New York: Van Nostrand Reinhold.
Wilk, M. B. (June 1955). "The Randomization Analysis of a Generalized Randomized Block Design". Biometrika. 42 (1–2): 70–79. doi:10.2307/2333423. JSTOR2333423. MR0068800.
