A pocket calculator program for Duncan's New Multiple Range Test and analysis of variance

A pocket calculator program for Duncan's New Multiple Range Test and analysis of variance

Cornput. B,ol. ,Mrd. Vol. 14, No. 3. pp 357-362, Pnnted in Great Britain. 1984 c 0010 4825’84 s3.00+ Ml 1984 Pcrgamon Press Ltd A POCKET CALCULATO...

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Cornput. B,ol. ,Mrd. Vol. 14, No. 3. pp 357-362, Pnnted in Great Britain.

1984

c

0010 4825’84 s3.00+ Ml 1984 Pcrgamon Press Ltd

A POCKET CALCULATOR PROGRAM FOR DUNCAN’S NEW MULTIPLE RANGE TEST AND ANALYSIS OF VARIANCE RICHARD Departments

of Medicine,

Biochemistry of Medicine,

A. LAWRENCE*

and Molecular Biology, Louisiana Shreveport, LA 71130, U.S.A.

(Receioed

13

State University

School

April 1983)

Abstract-A program for the TI-59 calculator to be used in analysis of variance and testing of significance ofdifferences between each mean and every other mean by Duncan’s New Multiple Range Test is presented. The test is both simple and powerful for data involving more than two treatment groups in a completely random design. Up to six groups with any number of replicates may be analyzed with this program. TI-59 calculator Multiple comparison

Duncan’s

New Multiple Range Test

Analysis

of variance

test

A problem that often confronts the biological investigator is the analysis of an experiment involving three or more treatment groups. Analysis of variance will indicate if there are significant differences among treatment groups, but often it is desirable to compare each treatment mean with every other treatment mean. Successive applications of Student’s t-test or the least significant difference (LSD.) to such a problem is inappropriate. Cochran and Cox [l] have indicated, for example, that in the extreme case when only the difference between the highest and lowest means is compared using the f-test or the L.S.D., the difference will be substantial even when no effect is present. It can be shown that with three treatment means, the t value calculated for the largest difference will be greater than the tabulated 5% level about 13% of the time, with six treatments 40%, with ten treatments 60’4, and with twenty treatments 90%. Thus, a test thought to be made at the 5% level is actually made at the 13% level with three groups, the 40% level with six groups, etc. Duncan [2] developed a test using a set of significant differences of increasing size depending on the closeness of the means after ranking. The program presented here uses Kramer’s modification [3] of Duncan’s New Multiple Range Test to allow for unequal replication in the treatment groups. However, when unequal replication is used the test is only approximate [4]. Following the computation of the analysis of variance, the procedure is: 1. Multiply S = error mean square by the appropriate tabulated Studentized significant ranges to obtain a set of intermediate significant ranges. 2. Rank the means in order from smallest to largest. Test the differences between means in the following order: largest minus smallest, largest minus second smallest . . . largest minus second largest, then second largest minus smallest, second largest minus second smallest and so on down to second smallest minus smallest. Each difference is compared to the corresponding intermediate significant range multiplied by [l/2 (l/r, + l/r,)]“’ where r1 and r2 are the number of replications in the two treatment groups being compared. 3. If the difference exceeds this least significant range then the difference is declared significant at the chosen level with one exception. No difference can be declared significant if

* Present address: The Audie L. Murphy Merton Minter Boulevard. San Antonio,

Memorial Veterans TX 78284. U.S.A. 351

Hospital.

Pulmonary

Disease Section,

11 lE, 7400

RICHARDA. LAWRENCE

358

Table 1. Effect of paraquat dose on 24 h urinary paraquat excretion

________________~_

____ -- ---.. ___-

PQ Dose

PQ Excreted

mglkg B.W.

p moles/ml

20

54 + 11* A

30

76210 101 +

40

l

____.-_- I_______-__

Mean+SEM

9 EC

123 + 4 C

50 --__---

AB

.____- _.__.._

Meansnotfollowedbythesameletterare

significantly different by Duncan'sNew Multiplerangetestat p c.05.

Table 2. .:8. I’ ,:i i3 ._a

Group

1 ‘3 13, 4 1 2 ::: ,

Group

14. 4!:1?~674i~l’~ 4

4

5; II

14 '::' _!_I1 .::; :z1 7,

!3’EM

5 5 E

Analysis

of Variance

1 1. 5 2 15 6 1I:I’~ '7. .-, c; Jl.

F Treatment d.f. Error d.f.

2~:3~4. I;I~::.Error Sum of Squares ~:&'~:~4i. ~51~:2 Treatment SS Total SS 5 43 iIl:3 . :~~y~:~ Studentized Significant Ranqes

‘3 L

Differences

101.

45

Mean

,>7e .

C’

I

4

Bet. Means

a

Duncan’s

new multiple

359

range test

Table 3. Press

Enter i.

Initialize

2.

Enter data for treatment group

4.

Repeat steps 2 and 3 for each treatment qroup.+ (If display flashes go to step 9)

5.

Compute

6.

Rank the means and :4 (rI + r2)llz for

SD and qroup

analysis

compute each comparison$

Enter significant studentized ranges (R) in order from largest to smallest 5

8.

Compute differences between and test for significancef

9.

If display flashes during data entry, reset raw data pointer by pressing D' and continue

pointer, + If raw

recording

4 For

A

1

Xi1

A

2

Xi2

XiJ

A

j

the

the

-

K’S

means

-

keyboard

or from

statistics

intermediate on magnetic

(or side).

XiJ

6

Mean, SEW

C

F, Treatment d.f., Error d.f., Error S.S., Treatment S.S., total S.S.

10

E

-

R's as

A'

-

Differences in order tested. Sig. differences followed by asterisks

magnetic manual

cards except

following that

B prints

instructions

D' resets

data

base

and

each

treatment

group

should

the

raw data

pointer

here

reset

Entered

-

cards,

To do this

SD,

D

D'

of the applied

is recorded

card,

mean,

SD,

and

in data

the raw

data

SEM.

be recorded

on

by pressing

a

D' after

data.

steps

the

column.

from

ST-06

B' compiles data

separate

$ These

be entered

program

Xi1

of variance

as

Entered

Xi2

SEM

7.

may

Data

t of

Compute mean, for treatment

entry

Printed

16

Entries

3.

* Data

Displayed

E'

may

table Read

the

R opposite

The

R in the

take

from

LSJ,

across the next

up to 3', minutes find

to the

degrees

column

protection previous

error

on

freedom

by the

desired

is the

depending of

headed

level

column

each

from

number

in the

second

the number

second

R, etc.,

ANOVA

of qroups column. back

of

treatment

output

in the

being

tested.

This

is the

to the column

groups. left

hand

Choose first

headed

R.

by 2.

it is included in a larger subset with a nonsignificant range, A more detailed discussion can be found in Steel and Torrie [IS]. This program computes the analysis ofvariance for up to six groups of any size followed by Duncan’s New Multiple Range Test. The user is required to enter the Studentized significant ranges (R) in order from largest to smallest from a table and the execution of two of the program segments requires up to 3.5 min each depending on the number of treatment groups to be analyzed. The program is written for the TI-59 calculator with print cradle and uses subroutines from the applied statistics library. It uses all 480program locations and all 60 data registers of the default partition when six treatment groups are analyzed. The program also calculates the standard deviation and standard error of the mean for each treatment group. A data summary from a sample problem is presented in Table 1 and the sample output using this program for this problem in Table 2. Differences between means are given in the order tested (see Step 2 above) and differences that are significant are followed by an asterisk. The user should make sure that no difference declared significant is contained within a larger subset with a nonsignificant range. Raw data or the intermediate data base can be recorded

360

RICHARDA. LAWRENCE

Table 4.

Duncan’s

new multiple

Table 4 continued

range

test

36

362

RICHARDA. LAWRENCE

on magnetic cards for future use as detailed in the applied statistics module manual for data entry program 06. Stepwise instructions for running the program are given in Table 3 and the program listing in Table 4. Studentized significant ranges can be found in Steel and Torrie [5] and other general statistics texts or in [2].

SUMMARY A program for the TI-59 calculator to implement Duncan’s New Multiple Range Test is presented. This test allows comparison of every mean with every other mean following analysis of variance in an experiment with completely random design involving more than two treatment groups. All of the necessary statistics are calculated for the analysis ofvariance and Duncan’s test and the data may be stored on magnetic cards for future use. This test is available in statistical packages such as SAS and SPSS if analysis of more than six groups is required. The results for the sample problem presented here agree with results obtained from SPSS.

Acknowkdgements-The author wishes to thank Dr. Thomas for testing the sample problem with SPSS.

J. Prihoda

for helpful suggestions

and comments

and

REFERENCES 1. W. G. Cochran and G. M. Cox, Experimental Designs, 2nd ed. John Wiley, New York (1957). 2. D. B. Duncan, Multiple range and multiple F tests, Biometrics 11, 1 (1955). Biometrics 3. C. Y. Kramer, Extension of multiple range tests to group means with unequal numbers ofreplication. 12, 307 (1956). 4. T. A. Bancroft, Topics in Intermediate Statistical Methods VI. Iowa State Press, Ames, IA (1968). New York (1960). 5. R. G. D. Steel and J. H. Torrie, Principles and Procedures ofStatistics. McGraw-Hill.

About the Author-RlCHmD A. LAWRENCE received his B.S. degree from Brigham Young University in 1971, and his Ph.D. degree from the University of Wisconsin, Madison in 1975. Dr. Lawrence then did postdoctoral studies at the University of Texas Health Science Center in Dallas and joined the faculty of the Department of Medicine at LSU Medical Center in Shreveport in 1978. Dr. Lawrence is presently Research Assistant Professor of Medicine at The University ofTexas Science Center in San Antonio. His major research interests are in the area of nutritional factors protecting against pulmonary oxygen toxicity. He is a member of the American Institute of Nutrition, the American Thoracic Society and Sigma Xi. He is an author of numerous scientific publications.