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University of Massachusetts Amherst University of Massachusetts Amherst
ScholarWorks@UMass Amherst ScholarWorks@UMass Amherst
Doctoral Dissertations 1896 - February 2014
1-1-1962
Stimulus durations and stimulus characteristics in paired-Stimulus durations and stimulus characteristics in paired-
associates learning. associates learning.
Calvin F. Nodine University of Massachusetts Amherst
Follow this and additional works at: https://scholarworks.umass.edu/dissertations_1
Recommended Citation Recommended Citation Nodine, Calvin F., "Stimulus durations and stimulus characteristics in paired-associates learning." (1962). Doctoral Dissertations 1896 - February 2014. 1445. https://doi.org/10.7275/60e8-hk39 https://scholarworks.umass.edu/dissertations_1/1445
This Open Access Dissertation is brought to you for free and open access by ScholarWorks@UMass Amherst. It has been accepted for inclusion in Doctoral Dissertations 1896 - February 2014 by an authorized administrator of ScholarWorks@UMass Amherst. For more information, please contact [email protected].
STIMULUS DURATIONS AND STIMULUS CHAHACTERI3TICS
IN PAIHED-A3S0CIATSS LEARNING
Calvin
A.B., Bucknell
M.A., Bucknell
P. Nodine
University, 1954
University, 1959
Thesis Submitted to
In Partial fulfillment of the
Doctor of
the Graduate Faculty
Hequirenients for the Degree of
Philosophy
University of lassaohusetts, Amherst
July, 1962
Acknowledgments
The author wishes to convey appreciation to the membersof his thesis committee, Professors A. E. Goss, C. C. Neetand J. W. Swanson. for their guidance in the preparation andcompletion of this manuscript. The author is particularly
indebted to Professor Albert S. Goss under whose direction a
major portion of the investigation was conducted.
The author's thanks are extended to the M.I.T. Computa-
tion Center, particularly to M. V. Solomita, Chief of Machine
Operations, for the use of the computer facilities.
Thanks are also due to Professor J. L. Myers and In Ho
Kim. Grace Craig, and J. R. Howell who made contributions in
various forms to problems concerned with statistical design
and computer programming.
In addition, appreciation is extended to Blase Garabino
who assisted in collection of the data, Joseph Mach for tech-
nical assistance with the apparatus, Helen L. Howell for
assistance in various aspects of the preparation and presen-
tation of the data and typing of the manuscript, Nancy Parrick
for aiding with data scoring, and finally to Professor Louis
Price and Barbara Nodlne for critical readings of the manu-
script.
iii
Table of Contents
Page
List of Tables and Figuresiv
Introduction1
3t and 8 DurationsM and Sim of Stimulus and* *?espoAse*Keabers* 1 ! ! ! ! ! ! iJ
Method13
SubjectsApparatus }^List !.*!!!!!!'.
^
Procedure !!!!!!!! }o18
Results20
St and a Durations^j,
Stimulus Characteristics ....!!!!!!!!!! iiDurations and Characteristics ..!!!!!!!.'.*.*!!!!!!!*
35
Discussion
DurationsRelationships among response members*!!!!!!!!! 41Present and previous findings 43Theoretical significance !!!! i^i
Stimulus Characteristics!
cqDurations and Characteristics ....!!!!!!!!!!!!!!!! 51
Summary
References
Appendix A. Data ^-^
Correct Responses on Hecall Trials 62!^ean Number of Correct Responses on
Anticipation Trials 78Response Latencies on Recall Trials !!!! 94
Appendix B. Instructions 110
Iv
List of Tables and Plgur^
TablePage
1.
162.
22
3.v^ui^Aji^ «xiuioj.pauion rests or '^rial Mlocks1 and 2 for Comblna^,ionG of Durations andStimulus Characteristics .... 23
«^. Means of Response Latencies during RecallTests of Trial Blocks 1 and 2 for Combi-nations of Durations and StimulusCharacteristics
22|.
$• Correlations between Means for H-^^call andthose for Anticipation and Latencies forSt Durations Singly and Combined 25
6. Analysis of Variance of Correct Responsesduring Hecall Tests of Trial Blocks 1 and 2 28
7. Increments in Means of Correct Responsesfrom Trial Block 1 to 2 for Combinations ofDurations and Stimulus CharacteristicsArranged to the Hi^rht and Downward in Orderof Increasing Ease of Learning 36
8. Ranges and Variances of Means of Correct Re-sponses for All Recall Tests and of Incre-ments in Means of Correct Responses fromTrial i31ock 1 to 2 for Combinations ofStimulus Characteristics within Com^>inationsof Durations of Decreasing Difficulty 39
Figure
1. Mean of numbers of correct responses forrecall and anticipation trials and of meansof response latencies for recall trials . .
.
21
Introduction
Experiments on effects of temporal attributes of thepresentation of stimulus and response members of paired-asso-ciate (PA) units have been infrequent and limited in scope.The primary objective of the present experiment, therefore,was to investigate PA learning as functions of duration of
presentation of the stimulus member of each pair alone (St
duration), and of duration of presentation of the stimulus
member and response member of each pair together (R duration).
Both meaningfulness (M) and similarity (Sim) of stimulus
and response members have pronounced effects on PA learning.
On grounds noted subsequently, it was hypothesized that dif-
ferences among acquisition rates for different combinations
of M and Sim of stimuli would be functions of St and a dura-
tions. The secondary objective of the present experiment,
therefore, was to obtain information about effects of stim-
ulus characteristics under different combinations of dura-
tions.
St and H Durations
Various theorists have assumed a parallelism between the
stimulus-response elements and relationships of classical
conditioning and those elements and relationships involved in
acquisition of the correct response of single PA units (e.g.,
Gibson, 19^0; Goss, Morgan, 'i. Golin, 1959; Spiker, i960).
Shown schematically for the anticipation technique of presen-
tation, the assumed parallelism is:
2
CS; presentation of stimulusmember, e.g., GEL
^j~
CR; occurrence of anticipation \response, e.g,, CIT \/\
UCR becomes anticipatbry (G!-{)
UCR: occurrence of response of sayingthe response member, e.g., CIT jA
UCS: presentation of response /member, e.g., CIT f
The stimulus member of a pair, which is usually selected
to have low or zero initial probability of evoking the re-
sponse of saying the response member, can be considered a CS.
When the stimulus member begins to evoke the response of say-
ing the response member before the response member occurs,
such anticipations can be considered CHs. The response mem-
ber and response of saying that member can be considered
analogous to the UC3-UCH relationship, i^ore specifically,
the particular relationship between exposure of stimulus and
response members which is schematized could be considered
homologous to classical delay conditioning in which the CS
appears before and remains on during the occurrence of the
UCS in contrast to classical trace conditioning in which CS
onset and offset is before occurrence of the UCS (Kimble,
1961, pp. 47-48).
Temporal variables have been rather extensively explored
In classical conditioning (Kimble, I96I, pp. 155-160). But,
despite the parallelism between classical conditioning and
the relationships of acquiring, the correct response in PA
3
learning, the St and H durations of PA learning have receivedlittle attention. Hegardless of the parallelism between PAlearning and classical conditioning, within the framework ofclassical associationism as well as for practical purposes,
such as design of teaching machines. Information is desirableabout PA learning as a function of St and R durations. How.
ever, in the last 50 years, only a few studies have been con-
cerned with the effects of these and closely related temporal
variables. In only three studies have both the St duration
and the i duration been varied (Hovland, 1949; Goss, Morgan.
& Golia, 1959; Wllcoxon, Wilson, & Wise, I96I).
Early attempts to investigate effects on PA learning of
temporal aspects of the presentation of stimulus and response
members were raainl^r concerned with strength of association as
a function of the interval between presentation of the stimu-
lus member and r^resentation of the response member using a
"trace conditioning" procedure. The criterion for acquisi-
tion was number of responses correctly recalled. Wohlgemuth
(1914) compared effects of simultaneous and successive pres-
entation of stimulus and response members. He discounted a
preliminary finding of the superiority of the successive
method on grounds that the total time for successive presen-
tation of each pair of stimulus and response members had been
twice that for simultaneous presentation of pairs. Twenty-
four color-figure pairs were presented under two conditions.
One condition was simultaneous presentation for twice as long
as successive presentation but with equal numbers of
4
preseatations. The other condition was equal length of pres.entation but twice as many presentations under simultaneousas under successive. Under both conditions, simultaneous
presentation produced better recall than successive. Unfor-tunately, Wohlgemuth presented either the stimulus member orthe response member of a pair as the stimulus for recall anddid not separate scores for backward recall from those forforward recall. Therefore, no general conclusions can be de-
rived from these data.
Froeberg's (I9I8) objection to the first condition of
presentation of Wolgemuth's main experiment was the apparent
assumption that strength of an association depends only upon
length of presentation of the stimuli regardless of conti-
guity or noncontiaiiity of stimulus and response members. In
Froeberg's first experiment, each 3 learned different 5-pair
lists of nonsense syllables under a simultaneous condition,
and under six different intervals between disappearance of a
stimulus member and presentation of its response member. The
successive intervals were from 0 to 5 ^ec. in l-sec. steps.
Stimulus and response members of a pair were each exposed for
.33 to .25 sec. Performance with the 5-sec. successive in-
tsrval was as good as performance with the 0-sec. interval.
However, on the average, there were 12; > more correct recalls
followin;j; experiences under the simultaneous than under the
six successive conditions.
Though the superiority of simultaneous to successive
presentation had not been significant, Froeberg considered it
sufficient to Justify a second experiment in which colors andletters of the alphabet replaced the nonsense syllables.With these materials, successive presentation was slightlybut not significantly superior to simultaneous, ^roeberg
attributed the superiority of successive presentation to the
requirement that with colors and letters each member of a
pair had to be attended to separately. In a further experi-
meat with the same materials. 3s read aloud 2-digit numbers
inserted between presentation of the stimulus and response
member of a pair "to eliminate the persisting memory images
during the interval- (p. l6l). Simultaneous presentation was
superior to successive with an irregular decrease in the num-
ber of correct responses for longer intervals between stimu-
lus and response members.
Guthrie (1933), in an experiment similar to Wohlgemuth' s,
had each S practice seven trials with figure-word and word-
figure series in counterbalanced order. These series were
presented under successive intervals of 2.55, 3.33, and 4.93
sec. between onset of a stimulus member and onset of its re-
sponse member. On the subsequent test, there was no differ-
ence between forward or backward recall of the words; the
longer the interval, the better the recall. Another group of
Ss was then run under simultaneous presentation of stimulus
and response members for Al sec. The mean number recalled
after training under this condition was greater than the means
for forward or backward recall after training with the 2.55-
sec. interval but less than means for the longer intervals.
6
In the Wohlgemuth, Proeberg. and Guthrie experiments,
Grier (I96O) contends, effects of temporal intervals of stim-
ulus and response terras were confounded with learning the
terms as such. In order to minimize the latter process, he
used seven letters of the alphabet as stimulus members and
digits from 2 to 8 as response members. The list was learned
with eight intervals between offset of stimulus members and
onset of response members from -2 to +5 sec. Stimulus and
response members of a pair were each presented for 2 sec.
Length of interval had essentially no effect on correct re-
sponses in the recall trial which followed the one learning
trial.
In these studies, acquisition was tested by one recall
trial; consequently, there were no learning curves. Also,
the "trace conditioning" presentation of stimulus and response
members differs markedly from the currently conventional
"delay conditioning" presentation of stimulus and response
members. Thus, the resultant findings are primarily sugges-
tive of the potential importance for PA learning of the in-
terval between offset of the stimulus member and onset of the
response member.
Suggestive of the importance of the St and R durations
are findings of comparisons of learning under prompting and
under confirmation conditions of presentation. Prompting has
involved presentation of the stimulus member simultaneously
or shortly before the response member. Confirmation resembles
trace conditioning: the stimulus member is presented and
removed, Hs anticipate the response .e.ber. and the response.e^ber is presented. In order to compare acquisition underthese two conditions, every nth trial is a recall test inWhich the stimulus members are presented alone. Thus, thetwo conditions represent variations in 3t durations with es-sentially equal R durations. In general, prompting has provedsuperior to confirmation (Cook, 1958; Cook & Kendler, 1956;Cook & Spitzer, 196O; Kopstein Roshal, 1955; Sidowski, K^p.stein, * Shillestad, 196I). Kopstein and Hoshal interpretedtheir results which favor prompting over confirmation as dueto longer R duration under prompting than under confirmation,
which may also be the basis of oidowski, Kopstein and Shil-
lestad's finding of fewer errors under prompting than under
confirmation. Cook and Spitzer note that the longer "S-R"
delay with confirmation than prompting may be a source of
interference with the association of paired stimulus and re-
sponse members. Limiting the usefulness of these results for
understanding effects of the St and R durations are the use
of only two St durations, and no manipulation of R duration.
The sSt and R durations were varied jointly, but in con-
founded fashion, in three studies. Hovland (19^9) used 1- or
2-sec. St durations with 1- or 2-sec. R durations, respec-
tively, to yield combinations of 1-sec. St and 1-sec. R dura-
tions (1:1 sec.) and of 2-sec. St and 2-sec. R durations {2:2sec.).
Kis major concern was whether practice was due to differences
in rate of responding. Under both distributed and massed
practice about twice as many trials were required to reach
8
criterion under the l:l.sec. duration than under the 2:2-sec.duration. Ho inforn^ation was provided on the interaction of'durations and distribution of practice.
aosa. Morgan, and Golin (1959) investigated PA learningas a function of percentage of occurrence of response members(^OHM) under 2:2- and 3:3.sec. durations. With 100^, 75:g,
50;^ and 25 5^ schedules, respectively, 511:. 85%, 103 and 60%more trials were required to reach a 7/8 criterion under the
2:2-8ec. duration than under the 3:3-sec. duration. The 7/8
criterion was less stringent than Kovland's two successive
perfect trials and there were various other differences be-
tween conditions of the two studies. Durations accounted for
843^ of the total variance of trials to criterion; but dura,
tions did not interact with ,^03M,
Wilcoxon, Wilson, and Wise (I96I) used lists of l^, 6 or
8 PA units which were each learned under 1:1-, 2:2-, and
sec. durations ^.'ith 100^, 50%, and 25% OHM. For all combina-
tions of length of list and %0m, there was a direct relation-
ship between speed of learning and length of St and R dura-
tions. In the analysis of variance of square-root transfor-
mations of trials to criterion, durations accounted for 76i
of the total variance.
All three studies suggest that St and H durations may be
important variables, at least with respect to trials to cri-
terion, though not necessarily with respect to total learning
time. Further, the results of the latter two studies sug.!;est
that the St and H durations may have greater relative effects
on trials to criterion than Xom, length of list, or dlstri-bution of practice. However, the confounding of 3t and Hdurations precludes infonnation about separate and joint ef.fects of these two variables.
The primary objective of the present experi..ent was toinvestigate the effects of independent variations of St dura,tion and R duration on PA learning. Thus both separate andjoint effects of durations could be assessed.
Several analyses of PA learning (e.g.. Sheffield. 1946;Underwood Schulz. i960) have distir^guished the process of'
learnirv?: or integrating responses from the process of associ-ating those responses with their paired stimulus members. In
addition. Goss. Nodine, Gregory. Taub, and Kennedy (1962) have
suggested that once responses are correctly associated with
their paired stimulus members, latency of those stimulus-re-
spouses associations must be reduced so that a response can be
evoked and completed in the St duration. Sta^dish and Champion
(i960) present curves which not only show a progressive in-
crease in speeds but also suggest that curves for easy items
are negatively accelerated throughout while those for hard
items are first positively and then negatively accelerated.
Brown and Huda (196I) report faster reduction of latency under
spaced than under massed conditions.
St durations may be so short that, even though a response
is correctly associated with a stiTiulus member, the response
cannot be evoked and completed within the time available.
Very short CS-UC3 intervals in classical delay and classical
trace conditioning pose the sa.e problem. Therefore, as inClassical conditioning, some procedure is necessary to deter-mine the degree to .^hich responses have been associated withtheir paired stimulus members somewhat indepenaently of la.tency of those associations and of limitations inherent inshort anticipation intervals. The procedure of the presentexperiment was a recall test after every five acquisitiontrials With an anticipation technique of presentation. Duringrecall tests each stinulus member alone was presented for l\r
sec, the longest St duration. Interpolation of recall-test
trials reduces mn from lOO;^' to 83.3,*; but available data
suggest that this should have little or no effect on acquisi-
tion rate (Goss, Morgan, & Golin, 1959; Schulz * Hunquist,
I960). In any event, the reduction was the same across con-
ditions.
M and Sim of Stimulus and Response Members
M and Sim of stimulus and response members are known to
influence rate of acquisition of correct responses of PA
units (Goss, 1963; Goss, Nodine, Gregory, Taub, i Kennedy,
1962; Underwood >k ;3chulz, i960). Acquisition rate is related
directly to M of stimulus and of response members with M of
response members usually more potent than K of stimulus mem-
bers. Acquisition rate is Inversely related to Sim of stimu-
lus and of response members with Sim of stimulus members usu-
ally more potent than Sim of response members.
Stimulus integration and response integration or strict-
ly, integration of responses to stimulus and response raembers
11
r asso-
on
er
are among the processes which presumably underlie effects ofSim and M of stimulus anc response members on PA learning(Goss. 1963). The earlier and more complete the integrationof response members, the sooner they are available fo
elation with appropriate stimulus members and for reductiin the latency of resultant correct associations. The earlieand more complete the selection and integration of responsesto the most distinctive features of stimulus members, the
sooner maximum differentiation of those members is achieved.
The more differentiated the stimulus members, the faster the
formation of associations between response members and appro-
priate stimulus members.
Integration of stimulus and response members should vary
directly with frequency and duration of experiences with
those members. Meaningfulness is conceived as a direct indi-
cant of integration of stimuli. Thus, the amount of further
integration of stimuli required in PA learning should be less
with stimuli of high M than with stimuli of low M. Increasing
St and R durations provides more opportunity for integration
of stimuli through rehearsal. Therefore, differences in
acquisition rates due to M of stimulus and response members
should decrease as functions of St and R durations.
With increasing Sim, more time should be necessary for
selection and integration of responses to the most distinctive
features of stimulus members and. perhaps, of response mem-
bers. Therefore, differences in acquisition rates due to Sim
of stimulus and response members should also decrease as
12
functions of 3t and R durations. Kor Sin, and H combined, theexpected effects are decreasing differences a»ong pairs rep.resenting different combinations of .;im and M of stimulus Indresponse members under progressively longer St and H dura-tlons.
13
Method
Subjects
Data are reported on 160 undersraduates drawn from theintroductory psychology courses at the University of Massa-chusetts. A total of 10 Ss, five males and five females, wereassigned to each of the 16 combinations of St and R durations
in order of his or her appearance. Each S was run individu-
ally by one of two male Es. One E ran three counterbalanced
cycles {kQ Ss); the other ^ ran seven counterbalanced cycles
(112 Ss).
Data on 12 additional Ss were discarded because of Es'
errors (N«3), apparatus failure (N^=2), 3s' failure to learn
by the end of the experimental session (M=6), or 3's failure
to follow instructions (N=l). Since these Ss were distrib-
uted among the 16 combinations of durations there is little
likelihood that the results were influenced by differential
elimination of Ss from some few combinations.
Apparatus
The apparatus components consisted of an electronic mem-
ory drum (Gordon H, Stowe Associates, Model 459B); a Hunter
Klock Kounter (Model 120); a Gerbrands electronic voice key;
and an i:;iectro-V^oice spherical microphone ( Jpherex 920).
Rotation of the .nemory drum and activation of the shut-
ter mechanism were electronically controlled in a manner which
permitted independent variation of 3t duration and R duration.
The drum was driven by a constant-speed electric motor.
During the presentation of each pair, the drum was held in astall position by a solenoid-operated escapement lever. Ac-tivation of the solenoid released this lever momentarily,
allowing the drum to rotate one step. Simultaneously, acti-vation of a second solenoid lowered the shutter for initial
concealment of the response member of the next stimulus-
response pair. After a specified duration had elapsed, de-
activation of the second solenoid released the shutter which
was returned to its original position by a spring to expose
the response member. After the specified duration of ex-
posure of stimulus member and response member together, the
solenoids were again activated to present the next pair.
When all pairs of the list had been presented the drum was
stopped and, after the intertrlal interval had elapsed,
started for the next trial.
The voice key and microp?ione were used to obtain laten-
cies of 3s' responses. A leaf-type microswitch was attached
to the shutter housing so that downward excursion of the
shutter started the clock. Since downward excursion of the
shutter and rotation of the drum were simultaneous, the clock
started as each stimulus member appeared. Speaking into the
microphone, which S held just below his mouth, activated the
voice key to stop the clock. When Ss failed to respond with-
in the St duration, release of the microswitoh by upward ex-
cursion of the shutter stopped the clock. The timer and
voice key were reset manually during the R interval prior to
rotation of the drum to the next pair.
15
List
The list was made up of 16 pairs of consonant-vowel-
consonant (CVC) trigrams. Each pair represented one of the
16 possible combinations of high or low Sim and high or low M
of both stimulus and response members. Table 1 shows these
pairs.
Particular combinations of Sim and M of response members
are coded by a letter code in which the first L or H indi-
cates low or high Sim and the second L or H indicates low or
high M. Combinations of 3ira and M of stimulus members are
coded in the same manner. Thus, any particular combination
of M and Sim of stimulus and response members is coded L or H
in each of the first two positions to indicate the values of
M and Slra of stimulus members and L and H in each of the last
two positions to indicate the values of M and Sim of response
members. Also, Sim of stimulus and response members are,
henceforth, abbreviated StSim and RSim, respectively, and M
of stimulus and response members are abbreviated 3tM and RM,
respectively.
Shown in parentheses after each trigram is its Archer
(i960) M value. These values ranged from 6i to 95%, Means
of the Archer M values for the trigrams representing the four
combinations of 1 and Sim of stimulus members are in the last
row. Means of Archer M values for the trigrams representing
the four combinations of M and Sim of response members are
shown in the extreme right-hand column. The means of from
86.00 to 92.25 for high M of stimulus and of response members
0)
HJO(A
Eh
a
x:ho
O
o
o09
co•H4JCC
C!•HjOBOO
4>
0)
(0
o
ao03
CO
<ft,
o
-PCO
•H
CO
U
s:
0)
CO
oCO
4)
03
o
•c!
CO
3
o
£3
Si
CO
ti
0)
e
CO
O
ca
0)
a;
a:
COOS)
5 S
c/3^
CVi
VOCM
Q
o00
:3t
Ml
oo CM
• • •On CM HiH CM
C3\ ?H CVi rH
O OiMMO <;
s
00H
QO
CM00 CO Ov
Q3< S <:
o o CMH CM
o JHO D OCO 3:
16
cn oCO o\
PQ •J
B M O OCO
CO*~««.
O ON00 On Csi
•••^
> CL> ooC5 Q
as
oo
oo•
NO00
(21) NO (22)
W•t>
?On
CN-
CM (93) (16)
•
H
PIX
(SI
o>
CUS YIB
o
ON
H
in
0)
O
cd
17
were at or close to the maximum attainable within constraintsimposed by the requirement that the stimulus and responsemembers be high or low Sim. The means of from 15.75 to 21.25for low M of stimulus and of response members were likewiseat or close to the minimum attainable within the requirement
of high or low Slra.
Within each of the two sets of four stimulus members of
high Sim and of the two sets of four response members of high
Sim. each member had a counterpart in reverse with which it
had three letters in common. Each member of a set also had
two letters in common with the remaining two members of that
set. V;ithin each of the two sets of four stimulus members of
low Slra and of the two sets of four response members of low
Sim, with three exceptions, no member had any letter in com-
mon with those of any of the other three members of the set.
E;xcept for vowels, there was no duplication of letters be-
tween sets of stimulus members of high Sim and of low Sim and
likewise for the sets of response members. The overlap of
vowels and consonants of the 16 stimulus members with those
of the 16 response members was minimal. Interlist Sim was at
or close to the minimum attainable within the requirement of
stimulus and response members of low and of high M,
Serial learning was minimized by the use of five orders
of the pairs for acquisition trials and four other orders for
recall-test trials. These orders of the pairs were deter-
mined randomly within the constraint that no pair was pre-
ceded by or followed by any one of the other pairs more than
18
on
once.
The pairs in the five different orders for acquisitl,were typed in pica capitals in a column down the center ofthe right half of a continuous tape. The stimulus membersalone in the four different orders for recall were typed ina column down the center of the left half of the tape. Whennot used, the pairs or the stimulus members alone were con-
cealed by a sliding metal shutter which covered one-half of
the aperture in front of the drum.
Procedure
The same list was acquired under all combinations of Zt
and of H durations of 1/2. 1. 2 and 4 sec.^ Intertrial inter-
vals averaged 8 sec. Pollowing instructions which described
the task (see Appendix B), Ss were administered blocks of
acquisition trials by the anticipation technique of presenta-
tion alternating with a recall-test trial. There were five
trials in each of the four blocks of acquisition trials.
During- these trials, only complete occurrences of the paired
response to each stimulus member during the St interval were
considered correct.
Following the fifth trial of each block of anticipation
trials, 3s were tested by presenting only the stimulus mem-
bers alone for recall of response members. In order to maxi-
mize the number of responses recalled correctly, regardless
1. Calibration of 1/2, 1, 2, and 4 sec. St durations and of Rdurations by an electronic timer yielded actual durationsof 0.51, 1.05, 2.07, and 3.86 sec, respectively.
19
of the combination of 3t and H durations for acquisition, ksec. wore allowed for recall of the response. On these
'
trials. Zs spoke into the microphone so that latencies ofrecall responses could be obtained. Only occurrences of thepaired response during the 4 sec. a particular stimulus mem-ber was exposed were considered correct.
In order to have an acquisition trial immediately beforeand immediately after each recall trial, following the last
recall trial, there was one more acquisition trial. Thus, in
all, 38 had 21 anticipation trials and four systematically
interpolated recall-test trials.
20
Results
The three response measures were correct responses toeach pair during each recall trial, mean number of correctresponses to each pair during the anticipation trial immedi-ately before and immediately after each recall trial, andlatency of response to each pair during each recall trial. A
latency of k sec. was assigned arbitrarily to failures to re-
spond and to incorrect responses. Figure 1 shows the means
for each of these measures for the entire list of 16 pairs
under each of the 16 combinations of durations through the
four recall trials and the four pairs of adjacent anticipa-
tion trials.
Each S's score could only be 0 or 1 for a recall trial
and 0, 0,5 or 1 for adjacent anticipation trials. By com-
bining the first two and last two recall trials and the first
two and last two pairs of adjacent anticipation trials into
first and second trial blocks, possible recall scores for
each pair were extended to 0, 1, or 2, and possible anticipa-
tion scores to 0, 0.5, 1, 1.5 or 2. Means of numbers of re-
sponses recalled correctly and of responses anticipated cor-
rectly for each pair in each trial block are shown in Tables
2 and 3 for all combinations of St and R durations and of Sim
and ^1 of stimuli. Means of latencies of recall responses are
presented in Table k.
Table 5 shows Pearson product-moment correlations be-
tween means for recall frequencies and those for anticipation
CO
o
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01
Table 5
Correlations between Means for Hecall and
those for Anticipation and Latencies
for St Durations Singly and Combined
St Recall-Anticipation
Recall-Latency
1/2 .00 -.98
1 .85 -.98
2 .96 -.99
.97 -.98
1. 2. k .88
1/2. 1, 2, k .87 -.98
26
frequencies and for recall latencies for the 512 cells ofTables 2, 3, and k for St durations separately and combined.No 3 was able to anticipate in less than 1/2 sec; conse-quently, the r for the relationship between means of recalland anticipation frequencies for the 1/2-sec. St duration was
.00. Difficulty in anticipating in less than 1 sec. may alsoaccount for the r of .85 for the 1-sec. duration in contrast
to the rs of .96 and .97 for the 2- and if-sec. durations. The
r of .88 for the 1-, 2-, and ^-sec. durations combined was
essentially unaffected by inclusion of the 1/2-sec. duration.
The latency means are essentially means of weighted frequen-
cies of correct recall, which, in part, contributes to the
high rs of -.98 and -.99 for relationships between means of
recall frequencies and recall latencies for durations sepa-
rately and combined.
These correlations were between means for the combina-
tions of stimulus durations and stimulus characteristics:
they are theoretically independent of correlations between
scores for response measures for individual Ss within each
combination of conditions. To estimate the extent of rela-
tionships between scores for response measures for individ-
uals within combinations, correlations for pairs of scores
for Individual Ss were computed for a sample of combinations.
For the relationship between recall and anticipation frequen-
cies, scores for individual were correlated for one of the
16 combinations of stimulus characteristics under each of the
12 combinations of ot and R durations, excluding St durations
27
se-
.on
of 1/2 sec. Such correlations were also computed between re-call frequency and latency for one of the 16 combinations ofstimulus characteristics under each of the 16 combinations ofSt and R durations. The particular combination of stimulus
characteristics under each combination of durations was
lected randomly within the constraint that each combinati.
of stimulus characteristics be represented only once.
The rs for recall and anticipation frequencies ranged
from .00 to .91. Only two were below .60, and six were .90
or above. All but one of the rs for recall frequency and
latency were -.90 or above; the remaining r was .00. Both of
the rs of .00 were with St duration of 1 sec. under which no
Ss either anticipated correctly or recalled correctly. On
the whole, for individual Ss within combinations of condi-
tions, recall frequency was related strongly both to antici-
pation frequency and to recall latency.
Because conclusions based on means for combinations
would be consistent with expected outcomes for individual Ss,
and because of the very high correlations between means of
recall frequencies and those for anticipation frequencies and
recall latencies, only recall frequencies were treated by the
analysis of variance summarized in Table 6. 3t and H dura-
tions were the variables of greatest importance; their ef-
fects, disregarding trials and then through trials (T), are
examined before considering effects of Sim and M of stimulus
and response members. Interactions of stimulus durations and
stimulus characteristics are then considered.
28
Table 6
Analysis of Variance of Correct Responses
during Recall Tests of Trial Blocks 1 and 2
Between SsStBSt X R
Krror (b)
Within SsStM
"
StM X 3tStM X RStM X St X H
StM X Ss/aStSimStSim X StStSim X RStSim X St X R
StSim X Ss/RMRM X StRM X RRM X St X RRM X Ss/
RSimRSim X StRSlffl X RRSira X St X RRSim X Ss/
TT X StT X RT X St X R
T X Ss/StSim X StMStSim X StM X StStSim X StM X RStSim X StM X St X R
StSim X StM X Ss/
339
144
36.34130.69
1.422.31
15.73**
I 80.00 190.48**3 0.48 1.143 1.58 3.76*9 0.43 1.02
144 0.421 44.25 80 . k5^-^
3 1.13 2.053 1.73 3.14*9 0.75 1.36
144 0.551 250.28 510.78**3 2.64 5.18*»3 1.29 2.63*9 0.72 1.47
144 0.491 132.61 210.49**3 0,153 1.05 1.679 0.34
144 0.631 402.75 1088. 51»»3 3.23 8.73**3 5.54 14.97**9 0.33
144 0.371 0.85 1.523 0.613 1.54 2.75*9 0.67 1.20
144 0.56
« £ <.05£<.01
a. Slash indicates nesting of between effects within each"within error.
*
29
bource
StM X RMStM XStM XStM X
HM X StHM X RRM X St X H
StM X RM X Ss/StM X RSimStM X asim X 3tStM X RSirn X RStM X RSlm X St X R
StM X RSlrn X Ss/TT X
XXX
StSlmStSimStSimStSini X
StSim X TStSim X RMStSim X RM X StStSim X RM A RStSim X HM X St X R
X Ss/
StT X RT X St X R
X Ss/
A RMRSim
StSimStSim XStSim X RSim X StStSim X RSim X RStSim X RSim X St a R
StSim X RSim X Ss/StM XTStM X T X StStM X T X RStM X T X St X R
StM X T X Ss/RSimRSim X StRSim X RRSim X St X RX RSim X Ss/
RM XRM XRM XRM X
RMRM XRM XRM XRM X
RMRSim XRSim XRSim X
X StX HX St X RT X Ss/TT X StT X R
RSim X T X St X RRSim X T X Ss/
StM X StSim X RMStM X StSim X RM X StStM X StSim X RM X RStM X StSim X RM X St X R
StM X StSim X RM X Ss/
VJ.X
1 11.063 1.543 0.779 0.44
0.711 0.043 1.383 0.149 0.26
n ii ii144 0.60X 4.173 0.613 1.459 0.43
144 0.271 0.753 0.933 0.469 0.18
144 0.401 6.763 0.363 1.559 0.28
•« 1.1.
144 0.471 2.203 0.013 0.279 0.12
144 0.4l1 5.463 1.033 1.659 0.30
144 0.451 5.913 0.073 4.239 0.49
144 0.311 7.363 0.013 1.669 0.21
n ! I.144 0.301 19.023 0.203 0.929 0.38
144 0.21
15.58**2.171.08
2.30
15.44**2.265.37**1.59
1.872.321.15
14.38**
3.30*
5.37*
12.53**2.293.67*
19.06**
13.64**1.58
24.53**
5.53**
90.57**
4.38**1.81
30
•J
StM
'Source
StM X StSim X RSimStM X StSim X RSim X StStM X StSiin X RSim X BStM X StSim X RSim X St X R
X StSim X RSim X Ss/StSim XT
StM X StSira X T X StStM X StSira X T X R
StSira X TX StSira XRM X RSimHM X RSim X St
StM X RM X RSim X RStM X RM X RSim X St X R
StM X HM X HSim
StM XStM
StM XStM X
XT
St X RX Ss/
StMStM
AX
TTTT
X Sa/
StRSt X R
StM X RM XStM X RM X
RM XRM X
StM X RM X T X Ss/StM X RSim XT ~
StM X RSim X T XStM X RSim X T XStM X RSim X T X
StM X RSim X TStSiin X RM X RSimStoim X RM X HSim X StStSim X RM X RSira X fl
StSim X RM X RSira X StStSira X m X RSim
StRSt X RX Ss/
StSim XStSim X
RM XRM X
StSim X EM X
TTT
X RX 3s/
StH
StSim X RM X T X St X RStSim X RI^ X T X Ss/
StSim X RSim X TStSim X RSim X TStSim X RSim X TStSim X RSira X TRSira
StSim X RSim X TRM X RSim X TRM X RSim X T X StRM X RSira X T X RRM X RSira X T X St X
RM X RSira X T X Ss/StM X
X StX RX St X RX Ss/
StM XStM XStM X
StSira X RM X RSiraStSim X RM X RSim XStSim X RM X RSim X
StR
StSim X RM X RSim X St X RStM X StSim X RM X RSim X Gs/
1*1 O
1 0.533 0.743 0.189 0.52
0.341 0.903 0.123 0.309 0.33
0.081 24.763 1.143 2.869 0.37
0.411 0.013 0.123 0.539 0.44
"1 I.I.
144 0.081 0.043 0.033 0.149 0.16
144 0.141 15.323 0.023 0.889 0.30
144 0,521 0.013 0.053 0.349 0.17
144 0.201 0.043 0.473 0.259 0.20
144 0.221 0.033 0.123 0.479 0.17
1 ii ii144 0. 241 9.613 1.023 0.309 0.13
144 0.63
F
1.562.18
1.53
11.25**1.503.75*4.12*»
60.39**2.78*6.98**
1.506.62*-^
5.50**
1.001.14
29.46**
1.69
1.70
2.141.14
1.96
15.25**1.62
31
Source
StM X StSim X RM XStn X St Sim X RM XStM X StSlmStn :: stsim
X RM XX RM X
TTTT
StM X StSim X RM XStM X RM X liSim X TStM X RM X RSim X T XStM X RM X RSim X T XStM X RM X RSim X T X
StM X RM X RSim X TStM X StSim X RSim XStM X StSira X RSim X
XrAXT
StRSt XX Ss/
R
StMStM X
StRSt X aX Ss/
T*"
T X St
StMSt Sim X RMStSlm X RMStSim
X RX Ss/
StSim X RSim X T X RStSirn X RSim X T X StX StSira X RSim X T
X RSim X TA lira X RSim X T X StX RM X RSim X T X R
StSim X RM X RSim X T X St X RStSira X RM X RSim X T X Ss/
StM X StSim X RM X RSim X fStM X StSira X RM X RSim X T X StStM X StSim X RM X RSim X T K R
StSim X RM X RSim X T X St X RX RM X RSim X T X Ss/
StMStM X StSim
df ir
1 1.0? 2.743 0.0?3 0,41 1.059 0.11
0.391 0.003 0.223 0.259 0.29
-1 )i )144 O.^i-l
1 3.51 9.00**3 0.49 1.263 0.119 0.30
0.391 2.54 10.16"-*
3 0.32 1.283 0.73 2.92*9 0.41 1.64
0.251 1.66 27.67**3 0.42 7.00**3 0.36 6 . 00**
9 0.34 5.67**0.06
3t and H durations. As shown In Figure 1, the curvesfor the 4:2, 1:^,. and 1/2:4 combinations of dura-tions through the four recall trials are negatively acceler-ated. However, for the 4:4 combination, even with 20 antlci-pation and three recall trials the mean of 14.00 for the lastrecall trial and the mean of 14.05 for the last pair of an-
ticipation trials were short of a perfect performance of 16
correct responses. The slope of the curve for the 4:4 corabi-
nation between Recall Trials 3 '^nd 4 was still relatively
steep so that perfect or near-perfect performance might have
been achieved with 5 or 10 more anticipation trials. The
corresponding slopes for the 2:4, 4:2, 1:4, and 1/2:4 combi-
nations were sufficiently less steep to preclude useful
graphic or visual estimates of the number of additional an-
ticipation and recall trials necessary for Ss to reach per-
fect or near-perfect recall.
The curves for the remaining 11 combinations, with the
possible exception of the curve for the 1:1/2 combination,
were still approximately linear. 'further, none had risen
sufficiently for satisfactory graphic or visual extrapola-
tion. The small number of points, relatively Halted seg-
ments of entire curves available for about half of the combi-
nations, and lack of a satisfactory rational basis were con-
sidered sufficient grounds for not fittlm^ the functions
necessary to estimate number of trials to perfect or asymp-
totic performances under each of the combinations of condi-
tions. Precluded, therefore, are comf>arison8 among combinations
33
of durations with respect to total amount of time to reacheither perfect or asymptotic performance.
In the analysis of variance, both 3t and H durations hadhighly significant effects with the latter the more potent
factor. Within each 3t duration, increasingly faster learn-
ing occurred with R durations of 1/2. 1, 2. and k sec. with-
in each R duration, increasingly faster learning occurred
with 3t durations of 1/2. 1. 2. and sec. The very small
mean square for the interaction of durations suggested that
each doubling of St and of H durations produced essentially
equal increments in numbers of correct responses. However,
each doubling of the ^ duration produced increments about
twice as large as those produced by each doubling of the St
duration.
The significant St x T and R x T interactions reflect
the greater differences among St durations and among R dura-
tions during the second trial block than during the first
trial block. The T x St x H interaction was not significant.
Stimulus characteristics . Highly significant ?s indi-
cated that responses recalled correctly were directly related
to M of stimulus and of response members and inversely rela-
ted to Sim of stimulus and of response members. The Fs fbr
the interactions of StM with StSlm and with RH were signifi-
cant as were the interactions of StSira with RSira and with HM,
The two interactions of particular importance are those for
StM and m and for StSim and RSim. The 3t7i x RM interaction
reflected increasing numbers of responses for combinations of
3^^
« of LL. HL. LH. and HH with pro.,ressively larger incrementsbetween each adjacent combination. The StSim x RSirn inter-action reflected increasing numbers of responses for cotnbina,
tions of Sim of HH, HL, LH, and LL with progressively largerincrements between each adjacent combination.
The significant StM x StSlm x m interaction reflected a
greater increment in numbers of correct responses from high
to low StSim with LH and HL than with HH and LL combinations
of M of stimulus and response members. A greater increment
in numbers of correct responses from high to low RSim with LH
and HL than with HH and LL combinations of l^. of stimulus and
response members gave rise to the significant StM x RM x RSim
interaction. Finally, the significant StSim x RM x RSim in-
teraction was due to a greater increment in numbers of correct
responses from high to low HSim with the LH, HH, and LL combi-
nations than with the HL combination of M of stimulus and re-
sponse members.
The significant interaction among all four stimulus char-
acteristics could be interpreted as due to progressively
larger differences among means for the four combinations of Ki
within combinations of Sim in the order LL, LH, HH, HL and to
progressively larger increments between adjacent combinations
of Sim in the order HH, LH, HL, LL.
All of the first-order interactions of each stimulus
characteristic with trials were significant from less than
.05 to less than .01. Some of the interactions of combina-
tions of stimulus characteristics with trials were also
35
significant. The pattern of relationships among means under-lying most, if not all of these interactions, was increas-
ingly large increments from the first to the second trial
blocks for successively easier combinations of stimulus char-
acteristics.
Durations and characteristics. Of the interactions in-
volvin£: durations and from one to all four stimulus charac-
teristics, disregarding and with trial blocks, 6 of 13 first-
order interactions, 6 of 10 second-order interactions, 5 of 8
third-order interactions, 3 of ^ fourth-order interactions,
and 2 of 2 fifth-order interactions were significant from
less than .05 to less than .01. The St x R x StSim x JtM x
RSlm X X T interaction was significant at less than .01.
The various significant interactions below the highest-
order interaction can be regarded as reflecting more promi-
nent features of the pattern of relationships among means
giving rise to the significant highest-order interaction.
Accordingly, rather than considering each of the former in-
teractions separately, the pattern of relationships underly-
ing the highest-order interaction is described. Table 7 pre-
sents increments in means of responses recalled correctly
from trial block 1 to 2 for the 256 combinations of durations
and characteristics. The 16 combinations of durations are
ordered downward in terms of increasing number of correct re-
sponses across all I6 combinations of characteristics. The
16 combinations are arranged from left to right in terms of
increasing numbers of correct responses across all I6
W
o
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ocnc\lv^^cvir^^^Hr^c\Jr^vovosoc^vo ^oooooooooooooooo oI I
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37
corflbinations of durations.
Proceeding downward, fco the right, or diagonally, the
increments are progressively larger. Shown in the last
column are means of increments for durations, disregarding
characteristics. Shown in the last row are means of incre-
ments for characteristics, disregarding durations. A rank-
order coefficient of .90 was obtained for the relationship
between means of increments and means of numbers of responses
recalled correctly through all trials under each combination
of durations. The rho was .31 for means of increments and
responses recalled correctly for each combination of charac-
teristics. The r between increments and means of responses
recalled correctly for all 256 combinations ves .54, which was
significant at less than .01. Thus the highest-order inter-
action reflected a pattern of increasing increments from the
first to the second trial block for increasingly easy combi-
nations of both durations and characteristics. Most of the
significant lower-order interactions involving durations and
trials, characteristics and trials, and durations, character-
istics, and trials can be regarded as special cases of this
more general pattern. The pattern also appeared in most of
the nonsignificant interactions but less markedly.
On the basis of an analysis of PA learning in terms of
stimulus Integration and response integration, the expecta-
tions were of decreasing differences in acquisition rates
among combinations of Sim, of M, and of Sim and M with longer
durations. When the same number of trials are administered
38
to all conditions, over-all acquisition rate can be expressed
as means of total numbers of correct responses. Instantane-
ous or "local" acquisition rate is indicated by increments in
means of correct responses from one trial block to the next.
Within each combination of stimulus durations, differences
among combinations of stimulus characteristics in either
over-all or local rates can be expressed as ranges or vari-
ances of means of numbers of correct responses or of incre-
ments in means.
In Table 8, combinations of durations are arranged down-
ward in order of Increasing means of responses recalled cor-
rectly. This order deviates slightly from the order for
total time of the sum of St and R durations, but the two
orders are highly correlated. Further, the order employed
allows for the relatively greater potency of R durations than
of St durations. Ranges and standard deviations of means of
correct responses for combinations of stimulus characteris-
tics within each combination of durations are shown, as are
means and standard deviations of increments in means from
trial block 1 to 2.
Contrary to expectations, as combinations of durations
became less difficult, ranges and standard deviations of
means of correct responses increased. Rank-order coefficients
of correlation of .66 and .53 were obtained for ranks with
respect to difficulty of durations and, respectively, ranges
and standard deviations for means of correct responses. The
ranges and standard deviations for increments in means of
39
Table 8
Ranges and Variances of Means of Correct Responses for
All Recall Tests and of Increments in Cleans of Correct
Responses from Trial Block 1 to 2 for Combinations
of Stimulus Characteristics within Combinations
of Durations of Decreasing Difficulty
eans of Correct ^iesponses Increments in Means
Range SD rtange 3D
1/2 1/2 1 6 0 . 6 1.87
1 1/2 0.9 2.16
1/2 1 1 7 7 OQ 0.9 2.62
2 1/2 2 0 1.5 3.70
1 1 i . N' 3.78
1/2 2 2.5 8.75 1.2 3.25
1/2 2.5 7.66 0.9 3.25
2 1 2.7 8.57 1.5 4.39
1 2 2.5 9.77 0.9 2.83
1 2.6 8.74 1.3 3.97
2 2 2.6 8.96 1.0 2.99
1 2.6 9.06 0.9 2.94
1/2 2.2 7.69 0.6 1.15
2 2.7 8.44 0.8 1.93
2 2.8 9.74 1.2 2.10
2.2 6.89 0.7 2.03
correct responses from trial block 1 to 2 first increasedwith decreasing difficulty of durations and then increased.
Consequently, the rank-order coefficients between ranks withrespect to difficulty and those for ranges and standard devi-ations were, respectively, -.1? and -.26. neither of which
was significant.
Discussion
The primary objective of the present experiment was todetermine the effects of St and of R durations on PA learning.
The secondary objective was, within combinations of durations,
to determine the effects of and Sim of stimulus and response
members on PA learning, h^indin-s for durations are discussed
first, then those for stimulus characteristics, and, finally,
those for durations and characteristics combined.
Durations
Means of frequencies and latencies of responses recalled
and of frequencies of anticipations on trials adjacent to re-
call trials were approximately direct functions of 3t duration
and of H duration. Each doubling of 3t and of ^ durations
produced approximately equal increments in means of responses
recalled. The increments produced by doubling R duration were
approximately twice those produced by doubling St duration;
thus, H duration was more potent than St duration.
Three details of these results are of interest: relation-
ships among response members, consistency between present and
previous findings, and the significance of these and previous
findings for theoretical interpretations of PA learning.
Relationships among response measures . For St and R
durations, disregarding Sim and M of stimulus and response
members, the family of curves through the four recall trials
for recall frequency and the family of curves for recall
latency were mirror images. The relationship between the
^2
family of curves for recall frequency and the family for fre-quency of anticipations was more complex. Por the level of
performance achieved in 25 anticipation and recall trials,
the 1/2-sec. St duration was simply too short for complete
anticipation responses to occur. Indeed, 3s were rarely able
to begin an anticipation response in 1/2 sec. l.ith the 1/2-
sec. St duration regardless of R durations, no correct an-
ticipations occurred. Whether at least some Ss would eventu-
ally be able to shorten their anticipation latency to the
200-300rasec. necessary for occurrence of a complete antici-
pation response prior to exposure of response members is con-
jectural. The shortest latency of recall responses achieved
in 25 trials was 800 msec.
Failure to anticipate did not mean that no learning had
occurred. In the l/2:l/2-8ec. and l/2:l-sec. combinations,
some correct responses were obtained on recall trials, and
their frequency increased slightly over trials. }]ore marked
increases in responses recalled correctly were obtained in
the 1/2:2- and l/2:4-sec. combinations. Thus, even with very
short St durations, with sufficient time to respond, there is
evidence of some, though slight, learning. Furthermore, for
progressively longer 3t durations, the curves for anticipa-
tion responses for the four R durations were increasingly
closer to the corresponding curves for recall responses so
that, for the 4-sec. St duration, there were essentially no
differences between pairs of curves for anticipation and re-
call responses in the 4:1/2-, 4:1-, 4:2-, and 4:4-sec.
43
combinations. Although no formal statistical test was em.ployed, comparison of the families of curves for recall andfor anticipation responses suggests an interaction amon:
durations, characteristics, trials, and response measures in
the form of greater divergence through trials of curves for
anticipation responses than of those for recall responses.
The range of means of anticipation responses was greater
than that for means of recall frequencies; but rank-orders of
means for durations, disregarding- characteristics, and of
means for durations and characteristics combined were compar-
able. :^he correlations between these means of recall and an-
ticipation responses for l-sec. 2-.sec., and 4-sec. St dura-
tions both separately and combined were from .85 to .96. Most
of the correlations between recall and anticipation scores for
individual 3s within a sample of combinations of durations and
characteristics were above .60 and half were .90 or above.
Thus, except for combinations involving the 1/2-sec. Jt dura-
tions, recall and anticipation frequencies for groups of Ss
and for Ss within groups were highly related. Even stronger
relationships were obtained between recall frequency and re-
call latency. On the whole, these correlations were suffi-
ciently high to suggest that only responses on recall trials
need be recorded. Furthermore, for si ort St durations, re-
oall trials provide evidence of the formation of associations
which cannot be obtained under an anticipation technique of
presentation.
Present and previous finding:s . The previous findings of
greatest pertinence are those of Hovland {19^9) for 1:1- and2:2-sec. durations, of Goss. r^organ and Golin (I959) for 2:2-
and 3:3-sec. cluratlons. and of Vilcoxon, WHson and Wise
(1961) for 1:1-, 2:2-, and 4:i^-sec. durations. ^or these
confounded St and R durations, trials to criterion was an in-
verse function of durations. Totals of times to criterion,
however, were essentially invariant.
In the present experiment, disregarding stimulus charac-
teristics. 57, 187. 263, and 412 correct responses were ob-
tained thr>ough all four recall trials with, respectively, the
1:1-, 2:2-, 3:3-, and k:k~3eo. combinations. The eightfold
increase in length of exposure to members of pairs of the kik.
sec. combination, relative to pairs of the l/2:l/2-sec. corabi-
nation, produced slightly less than an eightfold increase in
total number of responses recalled. However, by the third
recall trial, the curve for the k:k~sec. combination showed
negative acceleration and. by the fourth recall trial, was
fairly close to a criterion of perfect performance. In con-
trast, the curves for the 1/2:1/2-, 1:1-, and 2:2-sec. combi-
nations were not sufficiently high to show negative acceler-
ation and hence diminishing returns per unit of practice,
with more trials, therefore, numbers of trials to perfect
performance with 1/2:1/2-, 1:1-, and 2:2-sec. combinations
might increase over those for the 4:4-sec. combinations more
than 2. k, and 8 times, respectively. Por reasons noted pre-
viously, extrapolation of the curves obtained in the present
study to estimate trials at which asymptotic or perfect
^5
performance might be reached was not considered feasible.
Whether or not trials to criterion are inversely related to
St and to R durations, but total time to criterion is invari-
ant, oiust be determined by carrying Ss under each combination
of 3t and a durations to asymptotic or to perfect performance.
The 2:2-sec. combination is the conventional one for in-
vestigations of PA learning. The curve for this combination
was slightly above the middle of the families of curves for
recall and anticipation measures. A 2;2-sec. combination,
therefore, produces relatively representative performance.
However, should total time to criterion prove essentially in-
variant over a wide range of combinations of St and of i dura-
tions, considerable savings in Es' recording efforts can be
achieved by using combinations of longer durations which
should entail fewer trials.
Theoretical siRnificance . The present findings of ef-
fects of St and R durations are of theoretical significance
in terms of relationships between classical conditioning and
PA learning, and with respect to interpretations of the proc-
esses which enter into PA learning.
Parallels can be suggested between the elements and re-
lationships among elements of classical-conditioning situa-
tions and the elements and relationships among elements of
single units of PA learning situations. However, the present
findings do not suggest parallel effects of essentially the
same temporal variable, the CS-UCS interval in classical con-
ditioning and St duration in PA learning. For the purpose of
k6
comparison, the only satisfactory data from classical condi-
tioning- are those on frequency of conditioned eyelid closures
by human os as functions of the CS-UGS Interval m delay and
short trace conditioning. A 1/2-sec. Interval has generally
proved optimal (Kimble, 196I). The 20 anticipation trials of
PA learning of the present experiment are only one-third to
one-fifth of those usually administered in classical condi-
tioning of eyelid closure. Nonetheless, by the second block
of 10 trials of eyelid conditioning, most Ss make one or more
CRs. In contrast, anticipatory nonsense-syllable responses
were not even beginning to occur by the end of 20 anticipation
trials of PA learning. Moreover, in terms of nonsense-sylla-
ble responses anticipated and recalled correctly in the same
number of trials, acquisition rate and, possibly, asymptotic
performance were directly related to St duration.
One direction of reconciliation of findings of effects
of the CS-UCS interval and of St duration is to assume that
longer ;t durations allowed more frequent rehearsal of the
relationship between stimulus members and responses to paired
response members. Thus, lengthening St duration in PA learn-
ing would have the same effect as increasing the number of
trials in classical conditioning with a 1/2-sec. CS-UCS in-
terval. Unfortunately for the purpose of comparison, time
within a trial in PA learning is then equated with number of
trials in classical conditioning, furthermore, this inter-
pretation of within-trial events in PA learning provides no
reconciliation of findings of acquisition as a direct function
47
asof 3t duration with findings of poorer eyelid conditioningthe CS-UCS interval increased beyond 500 msec. Finally, at
least in the present experiment, most 3s did not report any
type of rehearsal during the interval in anticipation trials
when stimulus raembers were presented alone.
Implicit in the suggested reconciliation by means of a
direct relationship between .-t duration and amount of re-
hearsal is the problem of definition of a trial. Definition
of a trial as a single observed or inferred occurrence of a
particular response during or immediately after the presence
of a particular stimulus may approximate the most satisfac-
tory theoretical criterion of a trial. However, until some
better means of empirical or inferential specification of
single stimulus and response sequences is developed, the most
feasible criterion for a trial in i'k learning is overlapping
or immediately successive occurrences of stimulus and response
members or occurrences of one or the other alone for some
minimum duration, just as the most feasible criterion for a
trial in classical conditioning is paired presentation of the
CS and UCS or presentation of one or the other alone. By
these criteria of trials in PA learning and classical condi-
tioning, achievement for anticipatory responses during 20
trials of PA learning lags behind achievement for anticipatory
CHs during 20 trials of classical eyelid conditioning.
Underwood and 3ohulz (I960) propose two overlapping
stages of Pa learning: response integration and association
of a particular response to a particular stimulus. Cross
k8
(1963) suggests a third stage: reduction of latency of the
association between a particular stimulus and a particular
response.
With respect to response integration, it was suggested
earlier that lengthening <l duration should give Ss more time
per trial to rehearse each response member and thus hasten
integration and increase availability of response members.
Of Ss who experienced R durations of 1/2, 1, 2, and 4 sec,
^5%9 55%, 62%, and SZi, respectively, reported that, at some
time during acquisition, they rehearsed during the period
stimulus and response members were presented together. About
90% of Ss who said they rehearsed, reported rehearsing the
response member, rather than the stimulus member or both.
Thus, an important if not the primary basis of the direct re-
lationship between acquisition and ? duration is probably
greater response integration and availability due to more
opportunity to rehearse response members, and greater use of
this opportunity.
The data of the present experiment are of little value
for explicating the course of formation of associations be-
tween integrated, available response members and the stimulus
members with which they were paired. However, the discrepancy
between responses recalled and responses anticipated with,
particularly, the 1/2-sec. St duration, but also the 1-sec.
St duration, is corroborative of the notion of a latency-
reduction stage in PA learnin/;?. Although none of the 3s were
able to anticipate in 1/2 sec, during the longer time for
^9
response of the recall trial some correct responses did occur:correct associations had been formed but could not bo revealedin very short anticipation intervals. The superiority of re-
call to anticipation frequencies di.uinished with 1- and 2-sec.
St durations and essentially disappeared with the i+-sec. 3t
duration. However, the greater number of recall than of an-
ticipation responses with the two intermediate ,t durations
suggests that stronger associations between stimuli and re-
sponses had been formed than were indicated by frequencies of
anticipatory responses.
The greater potency of H duration than of 5t duration,
and also the tendency to rehearse response members, rather
than stimulus members or both, may have reflected essentially
the same weighting of factors presumed to underlie the greater
potency of M of response members than of il of stimulus mem-
bers. In conventional PA learning, all that is required is
differential recognition responses to stimulus members. Such
differentiation may oftentimes be merely noticing and respond-
ing to the particular one of the three letters of a member
which is different from the letters of most or of all of the
other stimulus members. But response members must be differ-
entiated from each other and differential recognition re-
sponses iTiust be integrated into units which can be rehearsed
readily and can be said during short anticipation intervals.
Because lengthening R durations allows greater opportunity
both for differentiation and for integration, IJ duration
should be more potent than St duration.
50
stimulus CharaoteristlGs
In the present experiment, effects of 51m and M of stim-ulus and response members on acquisition were less important£er se than as providln,, a ran«e of differences among the com-blnations in a rank-order reasonably consistent with otherfindings for those same combinations. Uisregardinc 3im, thedirect relationships between M of stimulus and of responsemembers and the greater potency of M of response members were
consistent with previous findings for mixed, partly-mixed,
and unmixed lists (Goss * Nodine, I962) as were, disregarding
M. the inverse relationships between Sim of stimulus and re-
sponse members. Contrary to previous findings. 31m of stimu-
lus members was less potent than Sim of response members.
The mixed list of the present study was the first in
which all 16 combinations of high and low M and Sim of stim-
ulus and response members were realized. The rank-order for
these combinations in a mixed list might be compared to their
rank-order in Goss. Nodine. Gregory. Taub and Kennedy's (I962)
Experiments lA and IB, In which each combination was repre-
sented by a different four-pair list. The correlation coef-
ficient obtained in this coraparlson was .68. The most impor-
tant difference in ranks was the much greater relative diffi-
culty of the combination of low and high Sim of both stimu-
lus and response members among the unmixed lists than of the
pair representing this combination within the mixed list.
Sampling of pairs representing particular combinations is the
probable basis for this and other discrepancies between ranks
51
of particular combiaations of Sim and M of stimulus and re-sponse members in mixed and unmixed lists.
There were, however, differences In the Joint actions ofstimulus Characteristics. With the unmixed lists, -.ost ofthe interactions among various combinations of Sim and ri ofstimulus and response members were nonsignificant. In the
present experiment with a mixed list, several of these inter-
actions. includln,2 the interaction of all four characteris-
tics, were significant: their pattern was progressively
larger differences between adjacent combinations for succes-
sively easy combinations.
The processes presumed to underlie effects of M and Sim
of stimulus and response members were described briefly ear-
lier; they are described more extensively elsewhere (Goss,
1963; Goss, Nodine, Gregory, Taub, 4 Kennedy, 1962). The
significance of effects on acquisition rate of stimulus char-
acteristics as such is primarily as confirmation and exten-
sion of Goss, Nodine, and Levitt's (196I) findings of differ-
ences in effects of Sim and M of stimulus and response mem-
bers of single paired associates (-experiments IV, V).
Durations and Characteristics
jixamlnation of the basis of the highest-order interac-
tion, the interaction involving 3t and R durations, all four
stimulus characteristics, and trials, revealad a relatively
si aple pattern. All 256 combinations of durations and charac-
teristics were arranged in order of increasin^^ numbers of cor-
rect responses through all four recall trials for the combina-
52
tlons of durations, and sioiilarly for the combinations ofstimulus characteristics. Increments from trial block 1 to 2were then calculated for each of the 256 conibinations a. ar-ranged in this manner (Table 7). ^or progressively easiercombinations of durations, of characteristics, and of both,the increments increased. The 256 combinations could be
viewed as producing differences among means during the firstblock of trials which were even greater during the second
block. While the Str^ X StSim x \m x iiSim interaction was sig-
nificant, within each of the combinations of durations rank-
orders of combinations of stimulus characteristics were essen-
tially the same. Thus, for pro ressively longer durations,
all 16 combinations of stimulus characteristics were displaced
upward, and differences among them became more pronounced.
Most of the significant lower-order interactions in-
volving trials also reflected Increasing increments from
trial block 1 to 2 for progressively easier combinations of
durations, of characteristics, or of both. Except for degree,
the same pattern of relationships among means was apparent in
many of the nonsignificant interactions. :i duration entered
into more significant interactions than did St duration. The
relationships producing significant interactions in combina-
tions of conditions involving 1 duration often occurred in
the same form in combinations involving 3t duration, but were
sufficiently attenuated to preclude significant interactions.
The direct effects of M of stimulus and response members
on acquisition rate have been interpreted as due to degree of
integration of recognition responses to those members.
Greater integration of recognition responses to stimulus mem-bars is viewed as allowing 3s more time for anticipation andfor rehearsal. Greater integration of recognition responsesto response members presumably provides a more complete unitfor anticipation earlier In acquisition and also allows more
time for rehearsal. Sim of stimulus and of response members
are also conceived as influencing recognition responses: the
greater the Sim. the greater the difficulty of forming stable,
different recognition responses.
Len^^thenlng St duration, R duration, or both can be re-
garded as providing increased opportunity for Ss to form
stable, different recognition responses to stimulus members
and to response members. Therefore, as durations lengthen,
all pairs representing combinations of stimulus characteris-
tics should benefit. In the present experiment, the combina-
tions which benefitted most from longer durations were those
which during the first half of the trials seemingly had the
most stable, dlscriminable recognition responses.
r-lost PA learning tasks, as noted above, require only
differentiations among stimulus members; but recognition re-
sponses to response members must be both Integrated and dif-
ferentiated. Accordingly, concentration on response members
and, as a consequence, relatively greater potency of R dura-
tions and of M of response members would be anticipated.
Supporting this anticipation were ^s* reports that their re-
hearsals were primarily of response members during exposure
5^
of stimulus and response members together.
St duration was probably of some importance with respectto opportunity to develop stable, differential recognition
responses to stimulus members. However, the marked discrep-
ancies between frequency of anticipation responses and fre-
quency of recall responses with the 1/2-sec. and 1-sec. St
durations, which diminished with the 2- and k^aec. St dura-
tions, suggest that the particular significance of St dura-
tion is simply providing sufficient tifne for associations
which exist in some strength to occur. ore generally, oppor-
tunity for single responses and chains of responses to occur
to stimuli is an obvious and important, but often overlooked,
prerequisite to occurrence of correct responses.
Effects of r\ and Sim of stimulus and response members on
acquisition rates were analyzed in terms of underlying proc-
esses of stimulus integration and response integration. The
expectations based on this analysis were decreasing differ-
ences in acquisition rates due to Sim, M, and Sim and n com-
bined for longer 3t and H durations. Some interactions of St
duration, and particularly of d duration, with stimulus char-
acteristics alone were significant; but the pattern of these
interactions which was of increasing differences with longer
durations vxas opposite that predicted.
The interactions of one or both durations with two or
more of the stimulus characteristics were interpreted within
the pattern of the si^rnificant interaction among St and R
durations, the four stimulus characteristics, and trials.
55
Differences among means of correct responses indicated by theranges and standard deviations of their distributions in-creased with decreasing, difficulty of 3t and H durations.
Differences among increments from trial block 1 to 2 increasedand then decreased with decreasing difficulty of durations.
Thus, the findings for differences among means of correct re-
sponses for the combinations of stiaiulus characteristics weredirectly contrary to expectations; and those for increments
of a form which had not been anticipated.
Other aspects of the findings, such as Ss' reports of
rehearsal during the period stimulus and response members
were presented together, are consistent with a response inte-
gration analysis of PA learning. In order to maintain a
stimulus integration and response integration analysis of PA
learning of simple form, the most plausible explanation of
the contrary findings is that Ss' mastery of the list under
the shorter Jt and R durations had not progressed sufficiently
to reveal maximum differences among means of correct responses
and among increments in means of correct responses for succes-
sive trial blocks.
56
on
re-
Summary
Acquisition of a list of 16 paired associates was inves-tigated as functions of orthogonal combinations of duratiof stimulus members alone and of duration of stimulus and
sponse members together, of meaning fulness of stimulus and ofresponse members, and of similarity among stimulus and among
response members. Bach of the paired associates represented
one of the combinations of high or low meaningfulness and
similarity of stimulus and response members. The durations
of stimulus members alone were 1/2. 1, 2, and 4 sec. and the
durations of stimulus and response members together were also
1/2, 1, 2, and 4 sec. Ten Ss were assigned to each of the
combinations of durations.
Pour blocks of five acquisition trials with the antici-
pation technique of presentation were each followed by a re-
call trial in which stimulus members alone were presented for
4 sec. The last recall trial was followed by one additional
acquisition trial.
The three response measures were number of correct re-
sponses and latency of responses on recall trials, and also
number of correct responses on the acquisition trial just be-
fore and just after each recall trial. Because high correla-
tions obtained between recall and anticipation frequencies
and between recall frequencies and latencies, statistical
analyses were performed only on recall scores.
Responses recalled correctly were a direct function of
57
duration of stimulus members, duration of stimulus and re-sponse members together, meaningfulness of stimulus membersand meaninsfulness of response members; they were an inversefunction of similarity among stimulus members and of simi.larity among response members. Duration of stimulus and re-sponse members together was more potent than duration of
stimulus members alone. Similarity among response members
had a more pronounced effect than similarity among stimulus
members. The same relationship held for meaningfulness of
stimulus and response members.
Various significant interactions amon^ durations, charac-
teristics and trials were obtained, including the interaction
among the two duration variables, the four stimulus variables,
and trials. Both this highest-order interaction and many of
the lower-order interactions involving trials were interpret-
able as increasing increments in correct responses through
trials for combinations of durations, of characteristics, and
of both which led to progressively larger means for all trials.
The results were considered consistent with an analysis
of paired-associates learning in which meaningfulness and
similarity of stimulus and response members are conceived as
acting through stable, discriminable recognition responses to
stimulus and to response members. Lengthening durations of
stimulus members alone and lengthening durations of stimulus
and response members to^^ether are presumed to provide greater
opportunity for occurrence and rehearsal of such recognition
responses.
58
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61
Appendix A
Data for Number Correct on Recall and Anticipation Trials andLatencies for each S on Trial Blocks 1 and 2 for each Combi-
nation of Stimulus Characteristics and Stimulus i^rations
Listed below are the numbers used in the Tables which
follow to designate each of the 16 combinations of high or
low Sim and M of 3t and R.
St R
Code Sim M Sim i 1
1 un rU H H
2 Txt
TLi H H
J un TLi L H
T Tll L H
5 H L H L
6 L L H L
7 H L L L
8 L L L L
9 H H H H
10 L H H H
11 H H L H
12 L H L H
13 H H H L
14 L H H L
15 H H L L
16 L H L L
62
O4)
oCO
o
oo
CM
00
0^
CM
CO omH O»H r-l
09
43
OCM OH OO OO HH OO OOo o o o o o o
o o o
CM
o o o o o o o
OO OO OO OO OO
o O O O O oOO OO OO OO
OO OO OO HCM HCM OO OO
rHOJ OH OO OO OO OO OCM
OH OO OO OCV OO OO OO
OO OO OO OO o
OO HO OO OO OO
O O H
OO OO OO HCM O
O O O O O CM
o O O o o O
o o o o o o
o o o o o o
O O O O H CM
CM CM O CM CM CM
o o o O O o
OO OO OO OO OO
OO OO OO OCM OO OO OH O O CO O O
OO OO OO OO OO
OO OO OO OO OO OO OO
OO OO OO OO O
O O O O O O
O O O O O o
OO OO OO OO OO
OO OCM OO OO CM H OH HCM
OO OO OO OO OO OO OO
O O O O O o
o o o o o o
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Cvi HCM HCM HCM HCM HCM HCM HCM
CM 00 ON
NO•HCVi rH<M OO OCvi
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63
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r-i O O O O O O
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CMCM HCM OH HO OH OO HH OCM OO OO
OCM OO OH OH OO OO HO OO OCM OCM
OCM OO OH OO OO OO OO OO OO OO
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CM ^ \0 00 c^
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OrH OO OO OO
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CM C^ 00 Ov
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HO H CM
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OH OO OH OO OO OO OO OH OH OO
CMCM OH CMCM OH CMCM H CM OCM OO OO OCM
OO OO HH OH HH OO HH OH OO OO
OCM OO OO OO OO OH H CM OO OO OO
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CM H CM H CM H CM H CM H CM H CM H CM H CM H (V
OH
65
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OCV OO CMCM rHCM OM rH r
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rHrH rHCvi rHOJ rHCM rHrH
OrH OO CMCM CMCM OCM rHCM rHCM OCM H CM H C^J
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OrH OO rHCM rHCM rHCM OO O rH O rH O O
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OO rHCM OO OCM OrH OO rH O O O O
rH CM r-i rH CM CM CM rHCM H CM rHCM rHCM rHCM
CM <r\ 00 O
tH
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rHrH
OrH
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00
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66
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o o
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i-t o orHCVi oo rHCM OO rH CVJ O rH OO O (NJ CM
rHCV OO HCV OrH OCM OOvj OO OO OCM OO
OrH OO OO OrH OCM OO OO OO OO OrH
OO OO OO OO OO CMCM OO OO OO OH
OH OO OO OO OO OH OO OO OH OO
OO OO OO OH OH OH OO OO OO OO
OO OO OO OO OO OCM OO oo OH OO
OO OH OO OO OO OH OH HC\1 OO OO
OH OCM OH OO OO OH OO OH OO OO
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67
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OH O O
OH OO OO OO OCVi OO OO 0(\"
H O
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HCM HPsJ HCM COCV
OCVJ OO OH HCNJ OCVJ OO HCM O CM H CM O CM
OO HH HCM OCM
rHO OO OCM OH HCM OCM OCM OCM OH OH
rHO OH OH OO OH OCM OO OO OC^J HCM
OO OO OO OO
OO OO OO OO
O OO OO CM CM OH
OCM OO HCM C^CM CMCM OCM OCM CMCNJ OO OCM
OO OCM OO HCM HCM OH OH O HH OO
OH OO HH OO OCM OH OO
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HCM HCM HCM HCM HCM HCM HCM HtV HCM HCM
1/5
CO
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On
00
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OO OO OO OrH OO O
OH CM CJ OrH OH OO O
68
OH HCM rHH CMCM CM CM H CV2 O H CM H H CM
OO OO OO OO OCM CMH O CM OO H CV2 OH
OO OO OO OH OOOO OO HH OO OO OO OO OO OH OO
H CM HCM HCM HCM H CM H CM OO
H CM O O
CM CM O OH OCM OH HCM CMH O r-
CM CMCM OO HCM HCM CM CV C\2 CM CMCM
H H CM O O
OH OH OO OO
OO OO OO OO OO OH OO OH OH OO
OO OH OCM OO HO OO OO HCV OH OO
HCM OO HCM OCM CMCM OCNJ CMCM HCV CMCM OCM
OH CMCM OCM HCM CMCM OCM HCM HCV HCM OH
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CM
H CMCMCM OCM CNJCM Of^ HCM CMCM OCM HO) CM<N2
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CMCM CMCM HH OO OCM HCM HCM OH CMCM CMCM
CM H HCM CMCM OO OO HCM OCM OCM HCM HCM
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70
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O CVJ
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HCM fXJJM CMCM OO OC\J M CM OH OH OO OCM
OH CMCM OCM HCM OCM OO OCM OCM OO CM CM
H H CSJ OH CM CM
CM OH OH OO OH OO OO OO OCM
H O O
OH OCM OH OO OO OO OO OH OO OO
O O O
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OH OCM OH HH OH OCM OO OO OO HH
OO HCM OH OO CMCM OH OO OO OO
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CM C^ vr\ MD CO crs
71
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CM
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CM
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CMCM HH CMCM HCM HCM CMCM CMCM OCM OO CMCM
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110
Appendix B
Instructions
This is an experiment in learning nonsense syllables andnot a psychological test. We are interested in certain com-plex relationships of the learning process common to allpeople, and are not concerned with your personal reactions.
When the task begins a shutter viill drop covering theright half of this vjindow. At the same time you will see anonsense syllable in the left half of the window. After ashort period, the shutter will go up presentin,<^ a second non-sense syllable. The two syllables together represent a pairwith the first or left-hand syllable as the stimulus and thesecond or right-hand syllable as the response. You are tolearn to associate the two syllables so that when the stimuluappears you can spell the response as quickly as possible be-fore the syllable for that response is exposed. There areseveral pairs of syllables. These pairs do not follow eachother in any regular order. The two syllables which make upeach pair, however, are always paired together.
An example is the nonsense syllable XYZ which first ap-pears alone for a short time, after which its paired responsePxiR, is exposed. Your task is to spell ?'-^R as soon as pos-sible after seeing XYZ and before the shutter goes up to ex-pose PQ,R. Try to say each letter as distinctly as possible.
Occasionally, there will be a trial on which only thefirst or left-hand stimuli appear. On such trials, keep re-sponding as before by spelling out the response to each ofthose stimuli as quickly as possible. No responses willappear.
l^hen you see each stimulus, if you think you know whatthe response should be, but are not sure, goiess because itwill not hurt your score any more than to say nothing and ifyou are correct it will be counted a success. If you don'tguess, or if you guess wrong, correct youriself by spellingthe correct response out loud as soon as it appears.
Please do not make up fanciful connections between thetwo syllat^les of a pair to assist your learning. Do not tryto use any special system in your learning; simply learn to
spell the response of each pair as soon as you can afterseeing the stimulus. Do you have any questions?
Seraember, as each stimulus appears, spell the response
to that stimulus as quickly as possible. If you are wrong,
Ill
correct yourself by spelling the response aloud as soon asthe response appears on the right.
Prior to each recall trial:
Now, only the stimuli will appear on the far right sideor the window. Respond as before by spelling the response toeach stimulus aloud as quickly as you can. You will see noresponses.