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Critical Flicker Frequency. The median It seems more likely that the improved per-
flicker fusion frequencies of the last three formance is largely attributable to compen-
trials starting below fusion and the last three satory motivation accompanying sleeplessness
trials starting above fusion were used in the While no systematic ratings of "effort e\-
analysis of the data. Inasmuch as the fusion pended" were obtained, general observation*;
frequencies from initial settings above and of S's test behavior and comments strongly
below fusion did not differ significantly, the suggested that the tests became more chal-
data from these two sources were combined. lenging as sleeplessness progressed. If the
The results of the Duncan test demonstrated higher standards of performance established
that the overall decline in CFF during the late in the sleepless period carried over to
60-hr, sleep loss was significant. However, the the recovery period, this would account for
significance of the decrease produced by the the superior performance after sleep loss. It
loss of one night of sleep was somewhat am- should be noted that improvement in per-
biguous. While all of the values of SL-2 were formance during and after sleep loss occurs,
significantly below all means on SL-1, they primarily, in those tests in which self-pacing
were not significantly below the value on R-l. is an important aspect of the task. This would
be expected if compensatory motivation were
DISCUSSION an important factor.
The absence of an independent control A differential effect on manipulation and
group and the failure of the performances travel movements produced by a psycho-
during the recovery period to return to the physiological stress seems to be clearly dem-
presleep loss levels make the interpretation onstrated in the panel-control task. This re-
of some of the data somewhat equivocal. In sult is in agreement with the earlier study in
the CFF, steadiness and leg movement tasks which the same task was used to appraise per-
and in the travel movements under normal formance changes accompanying food restric-
pacing, the level of performance is essentially tion. In both instances the deleterious effects
the same on SL-1 and during recovery. How- of the stress condition were confined to the
ever, the bimanual coordination test, both travel movements.
motion components on the panel-control test The data on travel movements in the panel-
under maximum pacing and the manipulation control task and the unimanual and bimanual
movements under normal pacing show a su- coordination tasks, in which travel movements
perior performance during the recovery pe- predominate, show consistent diurnal varia-
riod. tions during the three-day sleep loss period.
Within the design of the present experi- These observations, in conjunction with those
ment, the possibility that on some tasks detri- noted above, suggest that variations in "physi-
mental effects of sleep loss have been ob- cal fitness" produced by psychophysiological
scured or diminished by continued learning variations are reflected primarily in repetitive
during the sleepless period cannot be pre- travel movements rather than in other types
cluded. In the case of the bimanual coordi- of work movements. Such movements seem to
nation test, where no previous learning data be sensitive indicators of normal psycho-
is available, there is no objective evidence physiological variations as well as of the more
against this possibility. However, on the panel- extreme stress conditions produced by sleep
control task, if the results are considered in loss and nutritional deficit.
relation to earlier studies, it seems unlikely
that practice alone is adequate to account for SUMMARY
the improved performance on R-l and R-2.
Previous studies (Harris et al., 1958; Smith In this study the effects of 60 hr. of sleep-
& Smith, 19SS) indicate that the amount of lessness on various psychomotor and percep-
training given prior to the sleepless period tual performances have been investigated. The
should have been enough to lead to asymp- major purpose of the experiment was to de-
totic or near-asymptotic performance on both termine whether sleep loss produces differ-
motion components. ential effects on component movements of
Sleep Loss Effect on Human Motion 55
motion. The results may be summarized as panel-control task and the unimanual and bi-
follows: manual coordination tasks showed consistent
1. The loss of sleep had a differential effect diurnal variations during the three-day sleep
on manipulation and travel movements in a loss period.
panel-control task. The duration of manipu- REFERENCES
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sleep loss. Travel movements, particularly un- speed of leg and arm movements. / . appl. physiol.,
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crease in duration during the sleep loss period. DUNCAN, D. B A significance test for differences be-
2. Speed of performance in a test of bi- tween ranked treatments in an analysis of vari-
ance. Va. J. Set, 1951, 2, 171-189.
manual and unimanual coordination gave re- HARRIS, S. J. The effects of sleep loss on component
sults similar to those obtained for travel movements in human motion. Unpublished doc-
movements in the panel-control task. toral dissertation, Univer of Wis., 1955.
HARMS, S J , BROZEK, J , & S M I T H , K U. The ef-
3. Speed of a discrete leg movement de-
fects of caloric restriction on the travel and ma-
creased during the sleepless period. nipulation components of human motion Internal.
4. The number of contacts in a test of A. angew. Physiol. einschl. Arbeitsphysiol., 1958,
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S M I T H , PATRICIA A., & S M I T H , K. U. Effects of sus-
during the sleep loss period. No significant
tained performance on human motion. Percept,
change in the duration of contacts was ob- mot. Skills, 1955, 5, 23-29
tained. SMITH, K U., & WLHRKAMP, R A universal motion
5. A significant decrease in CFF was found analyze] applied to psychomotor performance.
during sleeplessness. Science, 1951, 113, 242-244
6. The data on travel movements in the (Received May 11, 1959)