Our natural environment is characterized by statistical regularities in both space and time — for example, it does not consist of randomly distributed light, but frequently contains objects that have elongated vertical and horizontal contours1 and predictable motion2. These regularities are exploited by our brains to interpret the often-ambiguous information that reaches our senses, to improve perception, decision-making and working memory. Although, in the natural world, past experiences can thus have a vital role in information processing and cognition, past experiences can impair performance in laboratory experiments that involve random structure. In a paper in Nature, Akrami et al.3 take advantage of this difference to identify an area of the rat brain that holds recent sensory history, and show that temporarily silencing this area removes history-related biases in memory-guided decision-making.
More than a century ago, the cognitive psychologist Harry Hollingworth identified a phenomenon called contraction bias4, in which the representation of a stimulus in working memory is systematically biased towards the average of recent past observations. As an example of contraction bias, consider Hollingworth’s historic experiment, in which participants were asked to judge the sizes of different cards. Subjects tended to overestimate the size of memorized cards if they were smaller than others used in the experiment, and to underestimate the size of memorized cards that were relatively large.
Akrami et al. first set out to show that, like these findings in humans, contraction bias governs the behaviour of rats. They trained rats in an auditory working-memory task, in which the animals had to determine which of two tones, delivered several seconds apart, was louder. This task requires rats to hold the loudness of the first tone in working memory during the delay period between the two tones, to enable comparison with the second (Fig. 1).
The authors used a custom-built, high-throughput facility for automated rat training and testing, allowing them to collect data from almost half a million trials. Analysis of the rats’ behaviour revealed that, in trials in which the first tone was the fainter, performance was improved if the previous trial had contained a pair of relatively faint tones, and hampered if it had contained louder tones. The group fitted powerful computational models to the rats’ behaviour that captured the animals’ recent sensory history. The models demonstrated that these systematic patterns of performance are predicted by contraction bias, which pulls the representation of the first tone (held in working memory) towards the recently experienced tones. In doing so, contraction bias facilitates or impedes the comparison of the two tones.
In a search for the site of working memory in the rat brain, Akrami et al. next made a truly exceptional observation. They temporarily silenced a brain region called the posterior parietal cortex (PPC), which has been implicated in working memory5, and found that overall task performance was improved by this intervention, particularly when the PPC was silenced during the delay period. This observed cognitive enhancement is clearly inconsistent with the idea that the PPC maintains the working-memory trace during the delay period, because silencing the PPC would erase the trace and hence lead to performance breakdown.
What underlies this remarkable improvement in performance during PPC silencing? Akrami and colleagues fitted their computational model to the rats’ behaviour during PPC silencing, and found that the improvement was due to a markedly reduced influence of past recent experience. Previous sensory information can distort working-memory representations. Therefore, in the randomized world of laboratory experiments, it makes sense that silencing a brain area that holds traces of sensory history can lead to more bias-free working-memory content and thus to behaviours more aligned with reality.
To directly test how PPC neurons encode the recent past, Akrami et al. recorded PPC activity during task performance. Consistent with their other results, the group found that, during the delay period, PPC neurons carried more information about the recent past than about the current tone held in working memory. Furthermore, across rats, the percentage of neurons holding such history-related information was tightly correlated with the level of history-induced bias in each animal’s performance.
It has long been recognized that even simple perceptual decisions are not isolated, static computations — rather, they are dynamic processes embedded in a stream of past information6. Akrami and colleagues have taken a crucial step towards understanding these processes, by identifying a node in the brain network that influences working-memory performance by holding a representation of recent history. That their discovery was made in an animal model offers the exciting possibility that future studies could investigate, at the cellular level, precisely which neurons in the PPC represent recent history, how this representation arises, and where and how it is integrated with sensory information to guide memory-based decision-making.
Statistical regularities not only influence working memory, but can also bias motor outputs and the encoding and decoding of sensory information7. It is therefore likely that history-related biases are implemented across many nodes of the decision-making brain network in addition to the PPC, through various mechanisms. Long-term mechanisms, on evolutionary and developmental scales, include the adaptation of neurons in sensory areas to the statistics of the natural environment. For example, the over-representation of vertical and horizontal contours in our visual environments is paralleled by an over-representation in the brain of neurons that respond preferentially to horizontal and vertical orientations8, and a biased ability to perceive these orientations9. Dynamic, short-term mechanisms occurring on a scale of milliseconds to seconds probably involve activity in long-range feedback or neuromodulatory circuits that adjust sensory areas10, the decision-making network11 and motor areas12. Elucidating the interplay between these mechanisms is just one of the remaining challenges in the quest to understand the powerful role of past experience in working memory.
Nature 554, 306-307 (2018)