S1 (FriAM 1-65) - The Psychonomic Society
S1 (FriAM 1-65) - The Psychonomic Society
S1 (FriAM 1-65) - The Psychonomic Society
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
Papers 144–150 Saturday Morning<br />
sults by the simultaneous use of task and temporal context representations<br />
to probe memory.<br />
8:40–8:55 (144)<br />
<strong>The</strong> Zero-Sum Trade-Off and Scallop Effects in Spacing Designs.<br />
PETER F. DELANEY, University of North Carolina, Greensboro, &<br />
PETER P. J. L. VERKOEIJEN, Erasmus University Rotterdam—<strong>The</strong><br />
present work explored two systematic within-list serial position effects<br />
that arise from including repeated presentations of items within<br />
a list: the zero-sum trade-off effect and the scallop effect. A zero-sum<br />
trade-off effect occurs when the height in the primacy region of the<br />
serial position function is inversely correlated with the height in the<br />
rest of the list. Unequal zero-sum trade-off effects across experimental<br />
conditions can be mistaken for other effects if primacy and recency<br />
regions are discarded from recall, or if ceiling effects occur in the primacy<br />
region. A scallop effect occurs when people use repeated long<br />
presentations to consolidate the preceding short presentations, as<br />
when several massed items follow several spaced items. <strong>The</strong> scallop<br />
effect results in some spaced items being better recalled than others,<br />
which can be confused with lag effects.<br />
9:00–9:15 (145)<br />
Exploring the Limits of Memory Access Control and Binding<br />
Mechanisms. MICHAEL S. HUMPHREYS, KRISTA L. MURRAY,<br />
& ANGELA M. MAGUIRE, University of Queensland—An analogue<br />
to the problem of remembering where you parked today, in the face of<br />
interference from prior parking memories, was instantiated by having<br />
participants learn a long list before learning a series of short lists.<br />
After each short list they received two cues. Both cues could refer to<br />
the short list (no-switch trials) or the first cue could refer to the long<br />
list and the second to the short list (switch trials). Each experiment<br />
made the task of focusing retrieval progressively more difficult. In the<br />
first experiment switch and no-switch trials occurred in blocks and in<br />
the second and third they were randomly intermixed. In addition, in<br />
the third experiment the same words were used in the long and short<br />
lists (an AB ABr paradigm, which requires a 3-way binding). In all<br />
three experiments participants were able to flexibly focus their retrieval<br />
efforts though it came with a cost.<br />
9:20–9:35 (146)<br />
Divided Attention and Repetition at Study: Effects on Group Recall.<br />
LUCIANE P. PEREIRA-PASARIN & SUPARNA RAJARAM,<br />
Stony Brook University (read by Suparna Rajaram)—Collaborative inhibition<br />
refers to the phenomenon that a group that works together<br />
performs worse than a nominal group where an equal number of individuals<br />
work alone and their nonredundant responses are pooled. We<br />
asked whether collaborative inhibition can be reduced under conditions<br />
where poorer or stronger individual memory changes the<br />
strength of individual organization. Participants studied categorized<br />
word lists and performed a free recall test in groups of 3 (collaborative)<br />
or individually (nominal). In Experiment 1, divided attention at<br />
study predictably reduced recall and weakened the individual subjective<br />
organization (ARC scores) of information. Critically, and as a result,<br />
collaborative inhibition also reduced following divided attention<br />
encoding. In Experiment 2, repetition at study predictably improved<br />
recall and strengthened individual subjective organization. Consequently,<br />
this opposite effect on organization also reduced collaborative<br />
inhibition. We discuss when collaboration can benefit or hurt individual<br />
performance and the role of individual organization in<br />
modulating this process.<br />
9:40–9:55 (147)<br />
<strong>The</strong> Ins and Outs of Memory: Written Versus Spoken Recall.<br />
RONALD T. KELLOGG, St. Louis University—Explicit memory is<br />
known to depend on input modality, with recent events showing a<br />
strong advantage when presented aurally rather than visually. <strong>The</strong> effects<br />
of output modality are less clear, but a writing deficit is plausible.<br />
In contrast to speaking, writing uses both phonological and or-<br />
23<br />
thographic representations that must be maintained in working memory<br />
for relatively long intervals due to slow motor output. It is also<br />
less practiced and automatic compared with speaking. Because writing<br />
makes greater demands on working memory storage and executive<br />
attention, it may reduce retrieval effort as a consequence. <strong>The</strong> evidence<br />
from word list recall is mixed, with some data even supporting<br />
the opposite conclusion of a writing superiority effect. However, recalling<br />
texts, complex visual events, autobiographical events, and category<br />
exemplars all show a writing deficit. <strong>The</strong>se tests all require a<br />
significant degree of retrieval effort that writing appears to disrupt.<br />
Cognitive Control<br />
Beacon B, Saturday Morning, 8:00–9:40<br />
Chaired by Keith A. Hutchison, Montana State University<br />
8:00–8:15 (148)<br />
Attentional Control, Relatedness Proportion, and Target Degradation<br />
Effects on Semantic Priming. KEITH A. HUTCHISON, Montana<br />
State University—Past research has demonstrated that target degradation<br />
effects (degradation � priming interactions) only occur when<br />
participants receive a stimulus list with many related items (i.e., a relatedness<br />
proportion, RP, of .50 or more). In this study, participants<br />
completed both an attentional control battery (Ospan, Antisaccade,<br />
and Stroop tasks) and a semantic priming task in which target words<br />
were presented either clearly or visually degraded and RP was manipulated<br />
within participants, within blocks using prime color to indicate<br />
the probability (.78 or .22) a to-be-named target would be related.<br />
Replicating Hutchison (2007), significant RP effects occurred<br />
and linearly increased with attentional control, indicating participants’<br />
flexible use of an effortful conscious expectancy process. However,<br />
overall target degradation effects occurred that were not dependent<br />
upon conditional RP or levels of attentional control, suggesting<br />
that degradation effects are not under participants’ conscious control<br />
and are a function of overall, rather than conditional, RP<br />
8:20–8:35 (149)<br />
Cognitive Control, Task Goals, and Memory. FREDERICK VER-<br />
BRUGGEN, Ghent University and Vanderbilt University, & GOR-<br />
DON D. LOGAN, Vanderbilt University—Cognitive control theories<br />
attribute control to executive processes that adjust and control behavior<br />
online. <strong>The</strong>ories of automaticity attribute control of skilled behavior<br />
to memory retrieval (MR). We contrasted online adjustments<br />
(OA) with MR, elucidating their roles in controlling performance in<br />
the stop-signal paradigm. We found evidence of short-term OA after<br />
unsuccessful stopping. In addition, we found that MR can slow responses<br />
for 1–10 trials after successful inhibition, suggesting the automatic<br />
retrieval of task goals. Based on these findings, we concluded<br />
that cognitive control can rely on both MR and OA.<br />
8:40–8:55 (150)<br />
Postconflict Slowing Depends on Relative Frequency of Conflict.<br />
WIM NOTEBAERT, WIM GEVERS, WIM FIAS, & TOM VERGUTS,<br />
Ghent University—Cognitive control processes impose behavioral<br />
adaptations after the detection of conflict (e.g., incongruent Stroop<br />
stimuli) and errors. <strong>The</strong> literature reveals that adaptation after conflict<br />
differs from adaptation after errors; after an error, reaction times increase,<br />
while this is not observed after conflict trials. An important<br />
difference between errors and conflict trials is the frequency of their<br />
occurrence: Whereas conflict typically occurs on 50% of the trials, errors<br />
occur with a much lower frequency. In this study, we investigated<br />
whether the frequency of conflict trials determines the occurrence of<br />
postconflict slowing. When conflict occurred on 25% of the trials,<br />
postconflict slowing was observed, but when conflict occurred on<br />
75% of the trials, slowing was observed after nonconflict (congruent)<br />
trials. This suggests that slowing is not triggered by conflict (or error),<br />
but rather by the detection of unexpected events. <strong>The</strong> results are discussed<br />
in terms of conflict monitoring theory.