One of the
reasons for starting a blog was that I wanted to occasionally write brief
summaries of papers that have influenced me along the way. In particular, I
wanted to write about papers that either might not have received a great deal
of attention when published, or older papers that I think still have a great
deal to offer. I’m starting with a paper
I hold dear, as it was the rock that I built my ramshackle PhD upon.
Logan, G. (1990) Repetition priming and
automaticity: common underlying mechanisms?, Cognitive Psychology, 22, 1-35
Repetition
priming is simply a change in behaviour to a stimulus you have previously
experienced relative to one you have not. For example, if I showed you an
object and asked you to classify it according to whether it was man-made you
would respond more quickly and accurately on the second compared to the first
presentation. So what? Firstly, repetition priming can be a big effect. You can
be as much as 200msecs faster on the second presentation of an object, a
potential 20% increase in speed [1]. Secondly, amnesics show intact priming,
despite being impaired at consciously remembering specific events (such as what
they had for breakfast that morning; referred to as ‘episodic’ memory)[2].
Thirdly, priming is long lasting – effects have been shown despite a gap of
several years between the first and second presentation of a stimulus [3]. So
priming seemingly taps into a mechanism(s) that learns quickly (following a
single presentation of a stimulus), lasts a long time (several years) and seems
to be distinct from ‘conscious’ or ‘explicit’ forms of memory.
What causes
repetition priming? There is plenty of healthy debate about the underlying
cause(s) of priming. Perhaps the most common idea though relates to the
learning of perceptual information when a stimulus is first encountered [4].
For example, when we see an object for the first time we construct a perceptual
representation of that object. On second presentation the existence of the previously
learned perceptual representation allows us to recognise the object more
quickly, speeding up any subsequent task performed on the object. Although many
argue about the specifics of such theories [5-6], most would agree that one
locus of repetition priming is perceptual in nature. If this is the case, it
shouldn’t necessarily matter what particular task we perform on the object each
time we see it; faster recognition = faster reaction times = repetition
priming.
Logan proposed a
completely different idea [7]. He suggested that when we see an object for the
first time and respond to the object, we learn a direct mapping between the
stimulus and response (an S-R association). When the object is seen for a
second time, we simply retrieve the S-R association learned on the first
presentation and quickly make the same response. Put simply, we don’t need to
figure out what response to make anymore as we just remember what we did last
time. This idea makes a clear prediction that ‘perceptual’ theories of
repetition priming do not. It predicts that if you have to respond differently
on the second presentation of an object relative to the first presentation,
repetition priming should decrease. In other words, you should only see
repetition priming when you are able to make the same response on the second
presentation. Across a series of 4 elegant experiments Logan clearly showed
this to be the case. When participants had to perform a different response
between stimulus presentations, or compute a new response following a switch in
task, repetition priming significantly decreased. He therefore provided strong
evidence for his view of repetition priming.
Again, why
should we care? Well, the two theories of priming outlined above are
fundamentally distinct learning mechanisms. One relates to perceptual learning,
one to associative stimulus-response learning. A phenomenon as robust and
ubiquitous as repetition priming deserves to be fully understood. This debate
is particularly important for fMRI studies of “neural priming”, where people
use an effect called repetition suppression or fMR-adaptation (a decrease in
the fMRI BOLD response to a repeated relative to a novel stimulus). Many
studies have presumed “neural priming” relates to perceptual learning within
visual regions. If Logan is correct, however, the effect they are measuring may
actually relate to the learning/retrieval of S-R associations and therefore may
not be telling us anything about perceptual learning per se [8]. Without being aware of this experimental psychology research,
it would be easy to confound perceptual learning with S-R learning by not
including a response manipulation within your experimental design. This is,
therefore, a classic example of how cognitive psychology and clever
experimental design can help inform more ‘neuroscientific’ studies of the same
underlying phenomena.
Finally, just a
quick note to say Logan wasn’t completely correct. It seems, as is often the
case, that repetition priming results from multiple learning mechanisms. One
does relate to the learning of perceptual (and conceptual) representations and
another relates to the learning of S-R associations [9]. As a result of Logan’s
original work we now have much clearer understanding of the multiple mechanisms
underlying repetition priming, as well as having much tighter experimental
control over these different contributions.
References:
- Horner, A. J., & Henson, R. N. (2009). Bindings between
stimuli and multiple response codes dominate long-lag repetition priming in
speeded classification tasks. Journal of Experimental Psychology: Learning,
Memory, and Cognition, 35(3), 757–779.
- Warrington, E. K., & Weiskrantz, L. (1968). New Method of
Testing Long-term Retention with Special Reference to Amnesic Patients. Nature,
217, 972–972.
- Mitchell, D. B. (2006). Nonconscious priming after 17 years:
invulnerable implicit memory? Psychological Science, 17(11),
925–929.
-
Schacter, D. L. (1990). Perceptual representation systems and
implicit memory. Annals of the New York Academy of Sciences, 608,
543–571.
- Tenpenny, P. L. (1995). Abstractionist versus episodic
theories of repetition priming and word identification. Psychonomic Bulletin
& Review, 2, 339–363.
- Bowers, J. S. (2000). In defense of abstractionist theories
of repetition priming and word identification. Psychonomic Bulletin &
Review, 7(1), 83–99.
- Logan, G. D. (1990). Repetition priming and automaticity:
common underlying mechanisms? Cognitive Psychology, 22, 1–35.
- Dobbins, I. G., Schnyer, D. M., Verfaellie, M., &
Schacter, D. L. (2004). Cortical activity reductions during repetition priming
can result from rapid response learning. Nature, 428(6980),
316–319.
- Horner, A. J., & Henson, R. N. (2008). Priming, response
learning and repetition suppression. Neuropsychologia, 46(7),
1979–1991.