scholarly journals Circadian Rhythm and Memory Performance: No Time-Of-Day Effect on Face Recognition

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Sergii Yaremenko ◽  
Melanie Sauerland ◽  
Lorraine Hope

The circadian rhythm regulates arousal and activity levels throughout the day and determines hours of optimal cognitive performance. Thus far, circadian fluctuations in face recognition performance received little attention in the research literature. The current experiment investigated the effects of time-of-day optimality on the ability to recognize faces and discriminate between the contexts in which where they were encountered. Morning- and evening-type participants (N = 91) encoded faces in a crime-related and a neutral context, either at their optimal or non-optimal time of day. Contrary to our hypotheses, neither face recognition nor source monitoring performance benefited from testing at optimal time of day. We discuss peculiarities of face processing that could account for the discrepancy of our findings with word recall and recognition literature.

1993 ◽  
Vol 4 (5) ◽  
pp. 326-330 ◽  
Author(s):  
Cynthia P. May ◽  
Lynn Hasher ◽  
Ellen R. Stoltzfus

Across two studies comparing younger and older adults, age differences in optimal performance periods were identified (Study 1), and then shown to be an important determinant of memory differences (Study 2). A norming study showed that while most younger adults were Evening or Neutral types, as determined by a standard questionnaire, the vast majority of older adults were Morning types. A second study compared the recognition performance of younger and older adults tested in the morning or in the late afternoon. Substantial age differences were found in the late afternoon, when younger but not older adults were at their optimal times. However, no age differences in memory performance were found in the morning, when older but not younger adults were at their peak period. Thus, synchrony between optimal performance periods and the time at which testing is conducted may well be a critical variable in determining group differences in intellectual performance, particularly between older and younger adults.


2016 ◽  
Vol 7 ◽  
Author(s):  
Stephanie M. Sherman ◽  
Timothy P. Buckley ◽  
Elsa Baena ◽  
Lee Ryan

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Sergii Yaremenko ◽  
Melanie Sauerland ◽  
Lorraine Hope

AbstractThe circadian rhythm regulates arousal levels throughout the day and determines optimal periods for engaging in mental activities. Individuals differ in the time of day at which they reach their peak: Morning-type individuals are at their best in the morning and evening types perform better in the evening. Performance in recall and recognition of non-facial stimuli is generally superior at an individual’s circadian peak. In two studies (Ns = 103 and 324), we tested the effect of time-of-testing optimality on eyewitness identification performance. Morning- and evening-type participants viewed stimulus films depicting staged crimes and made identification decisions from target-present and target-absent lineups either at their optimal or non-optimal time-of-day. We expected that participants would make more accurate identification decisions and that the confidence-accuracy and decision time-accuracy relationships would be stronger at optimal compared to non-optimal time of day. In Experiment 1, identification accuracy was unexpectedly superior at non-optimal compared to optimal time of day in target-present lineups. In Experiment 2, identification accuracy did not differ between the optimal and non-optimal time of day. Contrary to our expectations, confidence-accuracy relationship was generally stronger at non-optimal compared to optimal time of day. In line with our predictions, non-optimal testing eliminated decision-time-accuracy relationship in Experiment 1.


2020 ◽  
Vol 98 (Supplement_4) ◽  
pp. 60-61
Author(s):  
Elizabeth M Morris ◽  
Susanna E Kitts-Morgan ◽  
Dawn M Spangler ◽  
Kyle R McLeod ◽  
David L Harmon

Abstract Growing public interest in and use of Cannabidiol (CBD) in companion animals has amplified the need to elucidate potential impacts. The purpose of this investigation was to determine the impact of CBD on daily activity of adult dogs. Twenty-four dogs (18.0 ± 3.4 kg) were utilized in a randomized complete block design with treatments consisting of control, 2 mg CBD/kg BW/d, and 4 mg CBD/kg BW/d split between two treats administered after twice-daily exercise (7:00-9:00 and 17:00-19:00). Four hours each day (10:00-12:00, AM and 13:30-15:30, PM), were designated as time when no persons entered the kennels, with 2 h designated as Quiet Time and the other 2 h as Music Time, where calming music played over speakers. Quiet and Music sessions were randomly allotted to daily AM or PM times. Activity monitors were fitted to dogs’ collars for continuous collection of activity parameters. Data were collected over a 2-wk baseline period to block dogs by activity level (high or low) before randomly assigning dogs within each block to treatments. After 1 wk of treatment adaptation, activity parameters were collected for 2 wk. Data were tested for normality using the UNIVARIATE procedure in SAS before examining differences using the MIXED procedure in SAS, including effects of treatment, day, session (Quiet or Music), time of day (AM or PM), and accompanying interactions. CBD did not alter total activity points (P = 0.9971) or activity duration (P = 0.8776). CBD tended (P = 0.0692) to reduce scratching compared to control. Irrespective of treatment, dogs were more active in PM than AM (P < 0.0001). Regardless of session, dogs receiving 4 mg/kg/d tended (P = 0.0914) to be less active in the PM than control. CBD did not affect activity duration during exercise periods (P = 0.1425), but dogs receiving CBD ran more than control (P = 0.0339). These results indicate that when supplemented up to 4 mg/kg/d, CBD does not negatively impact daily activity levels of dogs.


2020 ◽  
Vol 4 (Supplement_1) ◽  
pp. 361-362
Author(s):  
Tara Johnson ◽  
Katie Stanko ◽  
Susan Jefferson

Abstract Destination memory errors (inability to remember to whom information was shared) affects all ages, but older adults are particularly vulnerable due to poor source monitoring. Individuals may assume information was already shared when it was not or repeat previously shared information. The current study explored two mental imagery strategies (vivid imagery, visualizing context) to improve destination memory. Using a software program, younger and older adults told randomly generated facts to random celebrity faces. Participants were unaware of the upcoming memory tests. The control group did not use a strategy. The imagery group used vivid imagery to connect the fact and face (e.g., visualize Oprah on a dime to remember Oprah was told that dimes have 118 ridges). The context group visualized a provided context (e.g., grocery store) when telling a fact to a face. Assessments of performance on item memory (facts, faces) as well as destination memory (face-fact pairings) were counterbalanced. Results indicated an associative memory deficit among older adults, which was driven by a higher rate of false alarms. However, across all adults, the vivid imagery condition was more accurate than the control condition, and they demonstrated fewer false alarms. These findings suggest that older adults can use mental imagery to reduce false alarms and improve destination memory performance. Implications include reducing age stereotypes, improving conversations, and decreasing potentially dangerous situations (e.g., withholding important health information thinking it already was shared with a doctor).


2019 ◽  
Vol 35 (05) ◽  
pp. 525-533
Author(s):  
Evrim Gülbetekin ◽  
Seda Bayraktar ◽  
Özlenen Özkan ◽  
Hilmi Uysal ◽  
Ömer Özkan

AbstractThe authors tested face discrimination, face recognition, object discrimination, and object recognition in two face transplantation patients (FTPs) who had facial injury since infancy, a patient who had a facial surgery due to a recent wound, and two control subjects. In Experiment 1, the authors showed them original faces and morphed forms of those faces and asked them to rate the similarity between the two. In Experiment 2, they showed old, new, and implicit faces and asked whether they recognized them or not. In Experiment 3, they showed them original objects and morphed forms of those objects and asked them to rate the similarity between the two. In Experiment 4, they showed old, new, and implicit objects and asked whether they recognized them or not. Object discrimination and object recognition performance did not differ between the FTPs and the controls. However, the face discrimination performance of FTP2 and face recognition performance of the FTP1 were poorer than that of the controls were. Therefore, the authors concluded that the structure of the face might affect face processing.


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