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Conen, K.

Publications and source records attributed to Conen, K..

2 recordsLinked to original sources

Nonhuman primates exhibit error type-dependent post-error slowing across modalities

Mistakes make up our daily lives. Once a mistake has been committed, it is common to pause before you continue. This slowing is called post-error slowing (PES). Although several theories have been proposed to account for PES in humans, findings across cognitive tasks show variation in how PES occurs, and it is unclear how this phenomenon may translate across modalities to a key model organism of human cognition, macaque monkeys. To determine whether monkeys exhibit PES, we tested three rhesus macaque monkeys in components of cognitive sequential decision-making tasks that used either eye tracking or touch screens to report responses. Here we show that monkeys exhibit non-adaptive, error type-dependent PES across modalities. Task structure and context also modulated PES in the eye tracking task, and no modality improved task performance following PES. These results suggest that monkey PES is a combination of cognitive and non-cognitive related responses to error that are modulated by task structures such as error type and task context. Overall, the flexibility in monkey PES is comparable to that of humans, further supporting the importance of monkeys as a translational model in investigating the mechanisms of PES.

neuroscience↗

Neuronal Adaptation to the Value Range in Macaque Orbitofrontal Cortex

Economic choice involves computing and comparing the subjective values of different options. The magnitude of these values can vary immensely in different situations. To compensate for this variability, decision-making neural circuits adapt to the current behavioral context. In orbitofrontal cortex (OFC), neurons encode the subjective value of offered and chosen goods in a quasi-linear way. Previous work found that the gain of the encoding is lower when the value range is wider. However, previous studies did not disambiguate between neurons adapting to the value range or to the maximum value. Furthermore, they did not examine changes in baseline activity. Here we investigated how neurons in the macaque OFC adapt to changes in the value distribution. We found that neurons adapt to both the maximum and the minimum value, but only partially. Concurrently, the baseline response is higher when the minimum value is larger. Using a simulated decision circuit, we showed that higher baseline activity increases choice variability, and thus lowers the expected payoff in high value contexts.

neuroscience↗