PART 1: Check whether the given data is Latin Square or
not?
This is a valid Latin square. There are two forms of nuisance Batch and
Day. There are five different ingredients being tested. In order to
control for the known nuisances, every ingredient must be tested one
time in each batch and on every day. This means that looking at the
Latin square, the treatments should only appear one time in every row
and one time in every column. Because this is the case, the Latin square
is valid.
PART 2: Linear Effects Equation for Latin Squares - RCBD:
\(y_{i,j,k} = \mu + \tau_{i} + \beta_{j} + \alpha_{k} + \epsilon _{i,j,k}\)
Where,
\(\mu\): Population Mean;
\(\tau_{i}\): Treatment effect for
population i;
\(\beta_{j}\) : Block effect for source
of Nuisance j;
\(\alpha_{k}\): Block effect for source
of Nuisance k;
\(\epsilon_{i,j,k}\): Error
corresponding to ith population, j&k blocks.
Hypothesis:
PART 3: Read the data into R, Convert the Treatments and Blocks as factors and finally perform ANOVA using aov().
Observations<- c(8, 7, 1, 7, 3,
11, 2, 7, 3, 8,
4, 9, 10, 1, 5,
6, 8, 6, 6, 10,
4,2, 3, 8, 8)
Batch<- c(rep(1:5, each = 5))
Days<- c(rep(seq(1,5),5))
Ingredients<- c("A", "B", "D", "C", "E",
"C", "E", "A", "D", "B",
"B", "A", "C", "E", "D",
"D", "C", "E", "B", "A",
"E", "D", "B", "A", "C")
Batch<- as.factor(Batch)
Days<- as.factor(Days)
Ingredients<- as.factor(Ingredients)
ANOVA_MODEL<- aov(Observations~Batch+Days+Ingredients)
summary(ANOVA_MODEL)
## Df Sum Sq Mean Sq F value Pr(>F)
## Batch 4 15.44 3.86 1.235 0.347618
## Days 4 12.24 3.06 0.979 0.455014
## Ingredients 4 141.44 35.36 11.309 0.000488 ***
## Residuals 12 37.52 3.13
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
Comment:
When the analysis of variance(ANOVA) was run, the p-value with respect
to ingredient was .0004 which is smaller than our alpha = 0.05. We can
say that there is evidence to reject the null hypothesis in favor of the
alternative hypothesis. At least one chemical ingredient has a mean
reaction time significantly different from the others.
We can also observe that the two blocks of predicted nuisance were not statistically significant. Our experimental design had less power than if we were to have designed the test without the blocks.
Observations<- c(8, 7, 1, 7, 3,
11, 2, 7, 3, 8,
4, 9, 10, 1, 5,
6, 8, 6, 6, 10,
4,2, 3, 8, 8)
Batch<- c(rep(1:5, each = 5))
Days<- c(rep(seq(1,5),5))
Ingredients<- c("A", "B", "D", "C", "E",
"C", "E", "A", "D", "B",
"B", "A", "C", "E", "D",
"D", "C", "E", "B", "A",
"E", "D", "B", "A", "C")
Batch<- as.factor(Batch)
Days<- as.factor(Days)
Ingredients<- as.factor(Ingredients)
ANOVA_MODEL<- aov(Observations~Batch+Days+Ingredients)
summary(ANOVA_MODEL)