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CIA RDP96 00789r003100140001 2
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Figure 2: A typical lucid dream initiated from a transient awakening during REM (WILD).
Salbrasons are 0 nV ands geese loved For Release 2000/08/08 : CIA-RD
LaBERGEAPRROME RHA Release 2000/08/08 : CIA-RDP96-00789R003100140001-2 (1b DREAMING 255 [125]
Table 1
Comparisons of Physiological Variables for Lucid and Non-lucid Epochs
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Vartables are averaged over REM Periods and subjects. L = mean value for lucid epochs; N = mean value
for non-lucid epochs; LND=mean value of difference score for lucid minus non-lucid epochs.
REM density (EM)
EML > EMN (t(12)=4.36; p<.0001]
EMLND > 0 [c(12)=3.93; p<.002]
Respiration Rate (RR)
RRL > RRN [(7}=4.07; p<.004]
RRLND > 0 [(7)=4.49; p<.004]
Heart Rate (HR)
HRL > HRN [(8)=2.54; p<.025]
HRLND > 0 [(8)=2.91; p<.01]
Skin Potential (SP)
SPL > SPN [(8) = 3.00; p<.01]
SPLND > [(8)=2.41; p<.01]
epochs of SVLD REM periods are characterized by significantly higher levels
of physiological activation than are epochs of preceding non-lucid REM from
the same REM period (see Table 1).
In order to follow the temporal variations of physiology correlated with
the development and initiation of lucidity, for each SVLD REM period the
physiological variables were converted to Z-scores and averaged across dreams
and subjects. Figure 3 is a histogram of the resultant mean Z-scores for the
ten minutes before and the five minutes after the initiation of lucidity. Note
the highly significant increases in physiological activation during the 30
seconds before and after lucidity onset.
Physiological data (EM, RR, HR, and SP) were scored for 61 control non-lucid
REM periods (NLREMPs), derived from the same 13 subjects, in order to allow
comparison with SVLDs (LDREMPs). Mean values for EM and SP were signifi-
cantly higher for LDREMPs than NLREMP controls (RR and HR did not differ).
If lucid dream probability (LDPROB) were constant across time during REM
periods, lucid dreams should occur most frequently in the first few minutes
of REM. On this hypothesis, LDPROB should be a monotonically decreas-
ing function of time into REM, following the survivor function of mean REM
period lengths (REMLEN). Although REMLEN proved to be an excellent
predictor of LDPROB (r=.97, p<.005), our data showed that LDPROB does
not reach its maximum before about five to seven minutes into REM. The
discrepancy between theory and observation is particularly acute for WILDs:
only one out of 21 WILDs occurred during the first four minutes of REM,
suggesting that there must be another factor contributing to the distribution
P96-00789R003100140001-2
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