Reputation: 21
Four common bean trials were established in fields, one trial per year. We combined density, bean genotype, and fungicide to manage white mold with a factorial scheme. The experimental design was a randomized complete block with four replicates. Each trial was analyzed by a three-way ANOVA. The fixed factors were density, genotype, fungicide, and interactions. The random factor was block.
My intent is to treat each trial as a form of replication, then I would like to combine all trials together in a more concise analysis. We don’t want to draw conclusions between trials. We want to make conclusions of in general about our treatments.
I have used the complex model with fixed and random effects like this:
y ~ DENS:GEN:FUNG + (1 | trials) + (1 | trials:block)
I would be very grateful if someone could tell me if the model is appropriate for my search.
Upvotes: 2
Views: 405
Reputation: 6867
The model:
y ~ DENS:GEN:FUNG + (1 | trials) + (1 | trials:block)
has the following features:
A fixed effect for the 3-way interaction DENS:GEN:FUNG
,
Random intercepts for block
varying within levels of trials
It is very rarely a good idea to fit a 3-way interaction as a fixed effect without the 2-way interactions and the main effects. See these for further discussion:
As for the random structure, then yes, based on the description, this seems to be appropriate, although you don't state how many trials
there are - if this is very few then it may be better to fit trials
as a fixed effect.
Upvotes: 1