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Thinking in and about time: A dual systems perspective on temporal cognition

Published online by Cambridge University Press:  25 September 2018

Christoph Hoerl
Affiliation:
Department of Philosophy, University of Warwick, CoventryCV4 8UW, United Kingdomc.hoerl@warwick.ac.ukhttps://warwick.ac.uk/fac/soc/philosophy/people/hoerl/
Teresa McCormack
Affiliation:
School of Psychology, Queen's University Belfast, BelfastBT9 5BN, Northern Ireland, United Kingdomt.mccormack@qub.ac.ukhttps://pure.qub.ac.uk/portal/en/persons/teresa-mccormack(024a3045-accf-42b9-8eba-65bb8b2bf6a7).html
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Abstract

We outline a dual systems approach to temporal cognition, which distinguishes between two cognitive systems for dealing with how things unfold over time – a temporal updating system and a temporal reasoning system – of which the former is both phylogenetically and ontogenetically more primitive than the latter, and which are at work alongside each other in adult human cognition. We describe the main features of each of the two systems, the types of behavior the more primitive temporal updating system can support, and the respects in which it is more limited than the temporal reasoning system. We then use the distinction between the two systems to interpret findings in comparative and developmental psychology, arguing that animals operate only with a temporal updating system and that children start out doing so too, before gradually becoming capable of thinking and reasoning about time. After this, we turn to adult human cognition and suggest that our account can also shed light on a specific feature of humans’ everyday thinking about time that has been the subject of debate in the philosophy of time, which consists in a tendency to think about the nature of time itself in a way that appears ultimately self-contradictory. We conclude by considering the topic of intertemporal choice, and argue that drawing the distinction between temporal updating and temporal reasoning is also useful in the context of characterizing two distinct mechanisms for delaying gratification.

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Copyright © Cambridge University Press 2018
Figure 0

Figure 1. Illustration of test trials in Clayton and Dickinson's (1998) study. In (a) 124-hour trials, scrub jays cached worms in Tray 1 and peanuts 120 hours later in Tray 2. After another 4 hours, they were allowed search in both trays. In (b) 4-hour trials, the birds initially cached peanuts in one tray and then cached worms in another tray after a 120-hour delay; 4 hours later they were allowed to search in both trays. Worms are the birds’ preferred food, but birds in the Degrade condition of the study received a series of pre-training trials in which they learned that worms had degraded after a 124-hour period. These birds preferentially searched for peanuts in 124-hour trials and worms in 4-hour trials. The figure contrasts the type of representation assumed to underpin the birds’ preferences according to an MTT account with that which is assumed by the temporal updating account. On the former account, the representations have tensed content that leads birds to infer that the worms are not edible. On the latter account, it is assumed that whether the birds’ model of the world continues to include a representation of edible worms in Tray 1 is governed by an interval timer.

Figure 1

Figure 2. Illustration of the tool-saving procedure in Kabadyi and Osvath's (2017) study, in which ravens preferentially select a stone that can be used to operate an apparatus to release food (Only part of the study carried out by Kabadyi and Osvath is described here). The figure contrasts the type of representation assumed to underpin the ravens’ performance according to an MTT account with that which is assumed by the temporal updating account. On an MTT account, birds infer the need for the tool by representing a future event in which they will re-encounter the apparatus. On a temporal updating account, the birds’ behavior is governed by a representation that includes information about objects outside of their current sensory scope (the apparatus) but does not include tensed content.

Figure 2

Figure 3. Illustration of the procedure in Cheke and Clayton's (2012) study for one pair of food types (peanuts and raisins). Boxes represent trays made available as caching locations; discs represent containers with food – black for peanuts, white for raisins. In the initial phase of the study (left-hand side of the figure), the birds were allowed to freely cache peanuts and raisins in two trays. In this initial phase, birds had not been pre-fed either food type. After a delay, they were pre-fed raisins and then allowed to retrieve from Tray 1. The pre-feeding of raisins meant that they no longer desired the raisins in the tray, preferring the peanuts. After a second delay, they were pre-fed peanuts and allowed to retrieve from Tray 2. The pre-feeding of peanuts meant that they no longer desired the peanuts in the tray, preferring the raisins. In the subsequent test trial (right-hand side of the figure), the birds were first pre-fed peanuts and were then again allowed to freely cache raisins and peanuts in both trays. The birds now preferred to cache peanuts in Tray 1 and raisins in Tray 2. On an MTT account, the birds infer that they should cache peanuts in Tray 1 on the basis of a representation of a future event in which they will find peanuts but not raisins desirable. On a temporal updating account, it is assumed that the birds update their model of the world, learning during the two retrieval stages that Tray 1 is a good place to cache peanuts and Tray 2 is a good place to cache raisins.