3 Novembre 2026

Psicologia Punto One | Psicologia e Psicologi nel Web

SCHEDA SCIENTIFICA2026Altra ricerca

Time Flows With the Changing of Events.

Matthew Logie, Marianna Lamprou-Kokolaki, Virginie van Wassenhove

Annals of the New York Academy of Sciences · 2026

Abstract originale

In recent years, investigations into the psychological experience of time have rapidly accelerated. The experience of time could depend on a ticking internal clock or rely on contextual changes within and between events. Cognitive theories of memory propose that the presence of event boundaries, as defined by unexpected changes, is crucial for the segmentation of sequenced content and ultimately, the formation of long-term memories. Interestingly, the experience of change also influences the temporal distances between memories. Concurrent lines of research have developed similar theories on the experience of time, with salient contextual changes distorting temporal experience. Herein, we propose a unification of theories from the fields of time and memory. Events are creatively constructed and encoded into long-term memory if sufficient changes occur. The subjective experience of time is also determined by an accumulation of changes creating temporal distances between memories. The encoding of memories provides temporal tags at multiple nested timescales, with no need to synchronize with the relative number of seconds that have passed, and duration estimates require a reconstruction of information between anchor points. Time does not exist without change, and experiencing change is fundamental for the formation of lasting memories.

Parole chiave

HumansCognitionTime PerceptionMemory, Long-TermMemorycognitioncognitive psychologypsychologysalientsegmentationtime perceptionunificationSegmentationPsychologyCognitive PsychologyUnificationSalient
Leggi il testo integrale originale

Testo estratto dalla pubblicazione: sono esclusi immagini, media, supplementi e parti soggette a diritti distinti.

Time Flows With the Changing of Events

ABSTRACT

In recent years, investigations into the psychological experience of time have rapidly accelerated. The experience of time could depend on a ticking internal clock or rely on contextual changes within and between events. Cognitive theories of memory propose that the presence of event boundaries, as defined by unexpected changes, is crucial for the segmentation of sequenced content and ultimately, the formation of long‐term memories. Interestingly, the experience of change also influences the temporal distances between memories. Concurrent lines of research have developed similar theories on the experience of time, with salient contextual changes distorting temporal experience. Herein, we propose a unification of theories from the fields of time and memory. Events are creatively constructed and encoded into long‐term memory if sufficient changes occur. The subjective experience of time is also determined by an accumulation of changes creating temporal distances between memories. The encoding of memories provides temporal tags at multiple nested timescales, with no need to synchronize with the relative number of seconds that have passed, and duration estimates require a reconstruction of information between anchor points. Time does not exist without change, and experiencing change is fundamental for the formation of lasting memories.

1Time and Memory

The human experience of time is driven by the tides of change, which appear to have an unchanging directionality; time flows from the past to the future and depends on memory for experienced changes. The brain segments present experiences and compresses and stores them in memory as episodes that define the past. Segmenting the continuous flow of experiential changes provides the anchor points for the encoding of memories, while the rate of change may define the distance between memories and, quite possibly, the experience of time itself. Herein, we argue that temporal experiences depend on the rate of change and the construction, compression, and encoding of information in memory. Specifically, our first claim is that parsing information is not parsing time: chunking a stream of information does not entail representing the interval spanned, which is a constraint that neither the discussed event segmentation theory (EST) [1] nor contextual‐change accounts [2, 3] state explicitly. While they assume that the event carries its own duration, we argue it does not [4, 5]. Second, we propose that time tags, and not durations per se, are the long‐term storage format for the when of memory: durations are distances computed between tags at retrieval. The computation of distances between tags has been argued for animal learning [6]; applying it to human event memory and deriving retrospective estimation from it is something the timing literature has not fully addressed [5, 7, 8]. Third, compression rate is the quantity that predicts underestimation. Information accumulated between boundaries sets a compression rate, so that the greater the compression of information, the greater the underestimation of duration. Focusing on the compression and imperfect reconstruction of information changes the functional relation between time and information that is distinct from the restatement of “more changes mean longer” typically found in the literature. Last, we suggest that attention acts as a sampling rate: attending to time increases temporal resolution. Altering the sampling of information alters compression, subsequent reconstruction, and the computation of temporal distances. An altering of the sampling of information between events provides a different prediction than the regular ticks of an internal clock of scalar expectancy theory (SET), since it should affect the reconstruction latency, not just the estimate [9, 10, 11].
 “It is utterly beyond our power to measure the changes of things by time. Quite the contrary, time is an abstraction, at which we arrive by means of the change of things” [12]

Theories of time experience within psychology have traditionally been based on the assumption of an internal clock [13, 14], wherein a pacemaker provides a stable temporal metric for the passage of time by counting ticks in an accumulator from which a duration can be derived. This model assumes a highly stable and stationary oscillatory mechanism to provide a consistent temporal metric, a requirement that is idealized and somewhat unrealistic in neural systems [7, 15, 16]. The notion of a centralized, dedicated timekeeping system is also not parsimonious, and neuroscientific implementations have not provided satisfactory accounts for multiple aspects of timing. Instead, alternative models, such as those proposing a decay rate of event memory across multiple time scales [17, 18, 19, 20] or state‐dependent networks in which the complexity of the network gives rise to timing [21, 22], seem to offer more biologically plausible implementations.

Given that time is not a physical quantity that can be directly perceived and measured, some models have adopted a more cognitive, information‐processing approach proposing that perceived duration is constructed based on perceptual content [23]. Behavioral evidence supports this view: prospective duration estimates increase with the number of perceptual changes occurring during an interval. More changes lead to longer perceived durations [24, 25, 26] and conversely, sensory adaptation to a constant rate of change results in a compression of perceived duration of subsequent stimuli [27, 28]. Perceptual time and duration in particular can be described in terms of the number of items [23] or changes in the stimulus [29]. However, in most studies, the definition of contextual change is highly limited and refers to simple, low‐level sensory features, such as pixel changes in a video stream [26]. While this sensory‐based, feedforward approach to temporal cognition has been appealing due to its similarities with magnitude perception, it often equates temporal experiences with sensory inputs, conflating information processing with timing. Indeed, it has long been suggested that the construction of duration depends not only on the number of items but also on how they are organized [3], and very few models in timing have incorporated this idea (but see [30]).

Herein, we would like to consider changes not as sensory features but as realistic atoms of computation for the estimation of time in real life, that is, as events and episodes. A crucial implication of this consideration is that an event has an extent in time [31]. Although life is experienced as a continuous flow of events [1], the contents of human memory are composed of temporally discrete episodes. These discrete events or episodes provide a key feature of human cognition that provides organizational principles for the structuration of events in the brain as opposed to sensory events. Additionally, we challenge an important limitation of traditional models that instantiate duration as the primary code for temporal processing, as they fail to account for temporal order. This is essential because event and interval timing have been dissociated as relying on a phase and an interval code, respectively [8]. Below, we will discuss how memory models can contribute to our understanding of how the brain represents time, not as the duration of events but through temporal tagging of events, which can be fully reconciled with a phase or an event‐coding scheme. In that sense, duration arises as a distance computation between two events in memory [6] and does not constitute the primary format by which time is encoded.

We will first introduce EST and accompanying notions of event boundaries and context drift. Then, we explain how these approaches can provide alternative views to the forward coding of temporal information as well as the recollection of the timing of events. We then report how the internal clock from SET cannot fully account for the estimation of durations and the when of memory. Last, we propose a pathway toward unifying theoretical accounts of time and memory.

2Event Segmentation: Hierarchical Time

The ability to hold and manipulate information within the mind at the present moment, such as the words within the current sentence, can be defined as working memory [32]. In contrast, episodic memory involves the encoding, storage, and retrieval of long‐term memories of autobiographical events [33]. Event‐based memory, as described by EST [34], is thought to be an account of the cognitive processes involved in creating events and seeks to explain the interactions that occur between working and episodic memory. EST proposes that the formation of episodic memories depends upon segmenting the continuous flow of information encountered throughout life. An event, a segment of experience with a specific spatiotemporal context, is represented in working memory as an event model, allowing predictions to be formed about what will happen next. When what occurs does not match the prediction, a prediction error is elicited, which acts as a trigger for encoding the contents of working memory into long‐term episodic memory [35]. Thus, EST provides a way to define long‐term memory whereby prediction errors act as event boundaries that demarcate the beginning and end of an event maintained within working memory, but also an episode encoded in long‐term memory. Crucially, information constructed in working memory can be lost without being subsequently available for reconstruction [36]. The absence of sufficient contextual change leads to a loss of information as clear events are unavailable for compression, encoding, and subsequent reconstruction from long‐term memory.

If an event boundary has been experienced, then memory tasks are necessarily testing information that has already been encoded into long‐term memory. Participants show poorer memory performance after experiencing boundaries that can be defined in terms of spatial or temporal gaps [37] because information has been cleared from working memory, requiring an (imperfect) reconstruction of the representation of the event [38]. Studies of walking through doorways support this interpretation [39], as do studies of memory for objects in films [40]. However, there is evidence that event boundaries can be defined solely in terms of contextual change without any prediction error occurring [41, 42]. For example, enhancing the predictability of boundaries by removing doorways suggests that improving predictability does not prevent the segmentation of events from occurring [43]. Long‐term memory performance and memory for temporal duration and order may thus be influenced by contextual shifts [44].

Interestingly, the process of event segmentation operates across multiple hierarchical timescales [45], from fine‐grained events at the sensory level to more high‐level, coarse‐grained segmentation [46, 47]. It is, therefore, unsurprising that segmentation at all timescales also appears to shape one's experience of duration. At the finest‐grained sensory level, unexpected or salient stimulus changes can affect duration estimates: studies demonstrate distorted temporal judgments for unexpected stimuli [48, 49, 50], including visual [51], auditory [52], and multisensory perception [53]. Even low‐level perceptual dynamics, such as object motion or saccadic eye movements, modulate time perception [25, 54, 55], likely by introducing segmentation points. At a mid‐level scale, physical transitions, like turning corners, walking through doorways, or entering new environments, act as segmentation cues that affect both memory and duration estimates [43, 56, 57]. Similarly, changes in musical structure that include nontemporal contextual changes mark the start and end of multiple bands of temporal sequences, such as unexpected changes in pitch (frequency) or loudness (amplitude) [58]. At higher scales, broader shifts in context, such as being at work, at home, or on holiday, serve as anchors for event segmentation and alter our sense of time [18, 59, 60].

Notably, segmentation is not limited to external sensory or contextual cues. Emotional shifts can also act as powerful markers of change, sometimes exerting stronger grouping effects than spatial or temporal cues alone [61, 62, 63]. In a study of segmentation, participants were presented with sequences of images alongside musical passages. Event boundaries were provided with changes in the music, such as valence or arousal. After 24 h, surprise memory tests were performed with a recognition test of old and new images and placing an image on a timeline. Participants were more accurate in placing an image on a timeline if the image had occurred at an event boundary, perceptual changes in music, valence, and arousal [61]. The study supports the view that events may be defined in terms of changes in context, and changes of context can be provided in a variety of ways.

Thus, contextual changes are a pervasive property of life experiences that help the segmentation of information at different hierarchical scales. The structuring of information into units (events, episodes) influences one's perception of time.

3Event‐Based Timing

One current major limitation of models of time is that they rely on sensory perception that uses an impoverished definition of event, which has not yet incorporated the event sequences of memory as described in EST [1]. Herein, we suggest that a similar event‐based account of memory is also an event‐based account of time perception [6, 64]. Accordingly, the subjective experience of time depends upon the computed temporal distances between events in memory without a dedicated duration storage.

Experiences of duration have long been proposed to depend upon the number and complexity of contextual changes that occur in both external stimuli and internal mnemonic activities [2, 3, 65]. Support for this view can be found in a study of task switching [66]. The subjective experience of time passing was examined by either providing a journal article to read, watching an entertaining sitcom, or switching between reading the article and watching the sitcom. Participants experienced the most time passing when watching the sitcom and the least time passing when reading the article. The experience of time passing for switching between the two occupied a middle ground between reading the article and watching the sitcom. One interpretation of the result could be due to the experience of contextual changes that accelerate contextual drift and create temporal distance between memories. From this perspective, the greater number of contextual changes experienced when watching the sitcom are the cause of the increased estimation of time passing. Notably, the results of task switching studies will depend on individual differences in the activities that individuals find engaging [67]. Additionally, the subjective experience of time can also be influenced by inhibition and mental updating [68]. Task switching, inhibition, and updating may be more generally described in terms of contextual shifts, which update the mental representations held within working memory, an interpretation that we will return to.

In the study of time perception, clear distinctions have been made between prospective and retrospective timing [69, 70]. Retrospective judgments depend upon the number of contextual changes that occur in a given interval, whereas prospective judgments also depend upon the allocation of attentional resources directed at keeping time. It is also noteworthy that cognitive systems crave information load [71, 72]. When information load is nonoptimal, false memories can be fabricated in order to fill the gaps [73, 74]. Based on studies of the construction of false memories, increased prospective duration estimates may be due to internal mnemonic activities during unfilled gaps rather than increased attention toward counting pulses. Accordingly, both prospective and retrospective judgments of timing are due to the number of contextual changes that occur. Contextual changes can be provided by both internal mnemonic constructions, such as structured thought and mind wandering, and perceptually salient stimuli. Differences between prospective and retrospective judgments may thus depend upon both internal and external contextual changes.

Evidence in favor of time and memory as a record of change can be found in studies based on behavioral work, computational modeling, and neuroimaging [75]. When comparing duration estimates of human participants and an image classifying an artificial neural network, both the humans and the neural network were found to produce similarly distorted duration estimates [26]. For the neural network, durations were recorded based on the dynamics of image classification determined by salient changes in sensory inputs, even though the network was not trained to mimic human duration estimates. The distorted duration estimates of both the network and the humans included perceiving short durations as longer and long durations as shorter than they actually were, which is consistent with Vierordt's law or the central tendency effects of Bayesian models [76]. Additionally, while matching the number of seconds of presentation, scenes that contained a lot of visual information were experienced as lasting longer than scenes containing less visual information. The duration of time was shown to depend on the dynamics of perceptual classification and the accumulation of salient changes as predicted by earlier models [2, 3, 23, 24, 29, 65].

A later study combined a behavioral and computational modeling approach to link salient perceptual change to prediction errors and working memory to episodic memory [18]. In the model, episodic memories were encoded if a sensory event did not match a prediction and successive events created a nested structure. The study demonstrated that both prospective and retrospective duration estimates depended on the number of predictable and unpredictable changes experienced. Prospective judgments were driven by the number of changes encoded, while retrospective judgments were driven by the number of changes recalled. Interestingly, for the computational model, duration estimates depended upon the rate of changes per second within a particular band of nested salient changes (i.e., perception or working memory or episodic memory). Similar duration estimates were found for human participants, supporting the interpretation of duration estimates and memory performance depending upon the most relevant layer of a nested record of change.

Altogether, these findings demonstrate that segmenting and hierarchically organizing events in memory across timescales is central to both memory and time perception. Accordingly, recent work continues to question the continuity in time [77], challenging the intuitive notion of continuous experience, in favor of discrete models of consciousness. From a perceptual awareness standpoint, this question is recurrent [5, 78] because it raises the question of how one moment may be distinguished from the next in the experiential flow of time. Indeed, evidence suggesting that experiential time relies on the endogenous structuration of (discrete) events is strongly counterintuitive, as it clashes with the phenomenology of a continuous flow of time. How then, in the face of EST, is a seemingly continuous experiential flow or chronology maintained?

4Context Drift and Ordinality

A fundamental basis for establishing the chronology of memories is the representation of context. Contextual representations drift at a certain rate, and the similarity of context determines temporal distances between items to be remembered. A theoretical account of this can be found in the temporal context model [79]. According to the temporal context model, contextual similarity provides a grouping effect in memory. Experiencing highly salient changes shifts the contextual representation, creating temporal gaps between groups of items which share a contextual overlap [80]. The rate of drift fluctuates based on the experience of change, and increasing the rate of contextual drift increases temporal distance even when no additional seconds have passed [57]. Additionally, experiencing event boundaries has been shown to provide a reset to the start of event context [81]. The segmentation of context both increases the number of items that can be recalled and improves memory for temporal order. Temporal clustering also improves memory performance for items that are close in time due to a shared context; items appearing further apart in time are separated due to a decreased contextual overlap. Furthermore, memory retrieval has been linked with the reinstatement of contextual detail [82], suggesting that such details can cue the retrieval of subsequent events in the stored memory sequence. As an example, when tasked with recalling short word lists, participants will tend to recall the words in a similar order to the order of initial presentation [83].

Overall, these studies point to a central role of temporal context in memory organization and performance. Supporting this idea, research on reading and narrative comprehension shows that readers perceive temporal shifts (e.g., “an hour later,” “the next day”) as event boundaries that help them structure the narrative in time [84]. Similarly, in studies using sequences of images with category‐based boundaries (e.g., switching between faces and objects), event segmentation impacts temporal memory performance [85, 86]. Crucially, temporal memory relies on context reactivation, which, in the case of an image sequence, is the reactivation of the representation of surrounding items [85]. Boundaries seem to disrupt temporal context by strengthening within‐event associations while weakening across‐event associations [85, 86, 87, 88]. It is also noteworthy that recent work describes the importance of neural drifts in the temporal structure of experiences [89, 90], although a direct causal link between neural drifts and the experience of time has not yet been established [91].

The presentation of contextual changes provided by spatial shifts has also been shown to influence the experience of time [92]. In this study, participants were presented with filmed scenes and asked to make estimates of how long each scene lasted. The scenes either displayed characters moving through doorways (spatial shifts) or characters moving without passing through doorways. Time estimates made at retrieval were found to be longer for scenes that contained spatial shifts than for scenes that did not contain spatial shifts. One interpretation of these data is that the spatial shift experienced when passing through doorways decreases contextual overlap, increases temporal distance between events, and acts as a temporal marker for memory. Similarly, in the study of spatial navigation [56], turns in a maze increased the recollected duration of the event.

The effects of contextual change have also been explored within virtual environments [74]. Participants were asked to remember paintings presented in different locations within a virtual reality environment. Memory performance for sequentially probed paintings depended upon the temporal distance between paintings without discrete changes provided by passing through doorways. The closer the temporal distance, the better the memory performance. Previous studies have also shown that contextual changes can disrupt memory for temporal order. While memory performance may be influenced by temporal clustering without the need for definite boundaries between clusters [43]. Boundaries defined by doorways, spatial gaps, and context shifts have been interpreted as driving segmentation by provoking a prediction error as described by EST [1, 40, 93, 94]. A recent virtual reality study highlighted how the quality (salience or distinctiveness) of spatial contexts define events and provide anchor points for the what of future memories [95]. Contextual shifts between distinct virtual contexts also provide strong anchor points for the when of memory, which influence the temporal distances between items in memory. Segmenting groups of images in distinct contexts provides structure for the temporal compression of memory, with images placed closer together on a timeline than originally presented. The compression occurred at nested scales both within each virtual room (event) and across the entire sequence [96, 97]. Not only were the items compressed, but items occurring earlier in an event were placed closer together than items occurring later within an event. The results provide evidence for the compression, encoding, decompression, and reconstruction of information within events driving the subjective experience of episodic time.

Note that while virtual reality can provide a particularly effective approach to studying segmented contextual change with tight controls on spatial and temporal gaps, emotional boundaries have also been shown to influence the temporal compression of memory. Compression depends on the sampling rate of information within events, which in turn determines subsequent temporal errors. A recent study showed that negative emotions drive an increase in the sampling rate, which reduces the compression of information and increases the subjective experience of time [98]. Taken to the extreme, negative emotions in depressive states may be defined as a dysfunction of segmentation. Recent electroencephalography work on rumination in depressive states provides further evidence for emotions influencing the sampling of information and the segmentation of events [99, 100, 101]. Beyond spatial and temporal gaps and changes of emotions, the memorability of the images themselves can drive segmentation effects. Memorability is a property of an image that determines how likely an image is to be remembered. Presenting a sequence of low memorability images followed by a sequence of high memorability images also provides a sufficient contextual change that alters the temporal distances between items in memory [102]. The compression and reconstruction of information determine the temporal distances between items in memory.

Hence, contextual changes (boundaries) provided by spatial shifts improve memory performance and provide anchor points for the temporal compression of information. Estimations of time also expand based on the sampling rate of information within events, which increases with negative emotions. Taken together, the result suggests that time depends on the sampling of information driving changes in how much contextual drift has occurred between boundaries. The concepts of space and time along with the concepts of valence and arousal of emotions may all contribute to the rate of change determining the compression of information and the subjective experience of time [103].

5Time and Nested Event Sequences

Rather than being encoded as informational content dependent on the number of items [32] or increasing noise [104], the contents of working memory may be encoded in terms of complexity of change [105]. Recent work has argued that episodic memory may be composed of multiple phases of temporally limited memory buffers [59, 106]. The episodic buffer [107] has recently been recharacterized as an awareness buffer [108] and could be further defined as a layer of episodic memory with the lightest compression and the shortest temporal limit [109]. The buffer may hold information in a lightly compressed state, maintaining accessibility for a fully decompressed processing of information within dedicated subcomponents of working memory. Single events are constructed within working memory. Experiencing sufficient contextual change drives the compression and encoding of an event into a phase of memory that can store sequences of compressed events, limited by the number of contextual shifts that can be stored [110]. Both the subjective experience of time and the formation of memories can be defined in terms of a record of change within nested sequences. With events encoded within successively longer‐lasting phases of memory [111]. Duration estimates and memory performance would then depend upon the rate of memory compression and the most relevant layer of the nested record of change [112].

Taken together, fluctuating rates of change may govern the subjective experience of time and the construction of memories by increasing temporal distance between mnemonic packets within nested temporal sequences. Time perception depends on the inherent complexity of capturing packets of information within cognitive systems, consistent with state‐dependent networks [22], as was also suggested by behavioral studies and computational modeling [75]. While memories may pass through phases of temporally limited episodic buffers [111], we must also account for how the temporal limits of memory are defined. One possibility, based on the study of entropy and Bayesian surprise [113, 114], is that memory processes involve tracking an accumulation of change; current contextual representations are compressed and encoded into longer‐lasting memory when the accumulation reaches a threshold. From this perspective, humans generate time with the processing of information and the encoding and reconstruction of a new experience.

6Boundaries, Context Drift, and the Experience of Time

An established account for the memory of durations and interval timing comes from the development of interval‐based internal clock models [14, 115]. SET [116] provides an influential account of an internal clock in which time perception depends upon an oscillatory pacemaker mechanism that generates pulses. The number of pulses generated within a given interval is read by an accumulator. The pacemaker, regulated by physiological factors such as arousal, starts when an event begins. Attention regulates the latency at which pulses are read by the accumulator and held within working memory. The current pulse count can be stored in a reference memory for comparison with subsequent counts. The system could also record the timing of multiple simultaneous events [117]. The initial formation of internal clock models could account for a linear experience of time. Studies employing psychophysical methods demonstrated that the subjective experience of time was not linear and could vary based on salient sensory stimuli [4, 118]. To account for variations in subjective time experience, attention was given the role of keeping track of pacemaker pulses, such that when attending to alternative stimuli, fewer pulses would be recorded. For example, if attention is distracted by sensory stimuli, pulses from the pacemaker may be missed, which provides an explanation for subjective time experience as the absence of attention to time yields to an underestimation of duration. While the findings on the underestimation of duration are robust, there are alternative theoretical explanations than that of a dedicated pacemaker, which we address in the following section.

One of the traditional theories on the subjective experiences of time comes from the concept of contextual change. The more contextual change experienced, the more time passes [2, 23]. One potential drawback of the internal clock account is the need for an observer that is dedicated to the clock [119]. This account leads to a similar issue faced within working memory research on executive functioning. Positing the existence of a central executive opened the possibility of an infinite hierarchy of managers described as internal homunculi [120] or decision demons that scream when a particular stimulus is perceived [121]. Much like approaches to explain executive functions and the complexity of cognition [122, 123], timing mechanisms may instead arise from the interaction of multiple networks rather than being dependent upon attention or a hierarchy of dedicated managers.

In favor of the interacting network view, subjective time experience can be found in the development of state‐dependent networks [21, 22]. The inherent complexity of interacting neural networks and the recurrent processes they produce may give rise to the subjective experience of time without the need for a dedicated internal clock mechanism. Indeed, online timing could be well accounted for by intrinsic synaptic scaling and temporal basis functions, such as those described in the cerebellum for subsecond timing [124]. However, they do not provide a mechanistic account of how durations are stored. Timing models strongly assume that time is coded as a duration in long‐term memory, thus that a magnitude (duration or interval) of time is available, namely, that a discrete storage of moments or scalar magnitudes is available. Such an assumption is congruent with observations of central tendencies and priors in duration estimation, given a learned set of durations in the lab that can be contextually modulated [125] or even stronger societal priors observed in single‐shot retrospective time estimations in real‐life experiments [126, 127]. The storage of durations is also congruent with recent work suggesting that sequences of durations can be held in working memory [128, 129].

The experience of time passing has also been shown to depend on the intensity of changes in ongoing visual perception [130]. In that study, participants viewed a starfield (provided by colorful dots traveling on a screen) within which the velocity and density of stars along with the duration of the viewing experience could be manipulated. Both the velocity and the density of the stars altered the experience of the passage of time. A higher rate of change provided by increasing the velocity or density of the starfield accelerated time such that more time was experienced. However, manipulating the number of seconds that participants viewed the starfield did not affect the experienced passage of time. Similarly, duration and passage of time are affected by the rate of events. Increasing the number of events lengthens duration estimates, and the rate of change accelerates the passage of time. Duration estimates required longer reaction times than passage of time judgments, suggesting that duration estimates may require a reconstruction of the number of changes that occurred [131]. In a previous study, paying attention to time lengthens duration estimates, whereas not attending to time shortens estimates. Additionally, increasing the load placed on working memory leads to reductions in duration estimates [132]. From a contextual drift perspective, the quantity of information accumulation within an event alters the passage of time by increasing contextual dissimilarity, which determines temporal distances and the rate of compression of information, which leads to an underestimation of duration. See Table 1 and Figure 1.

The subjective experience of time can be explained as a result of task engagement or in terms of curiosity for seeking out new experiences, which can provide us with prediction errors and improve our future predictions. In this case, the best forms of media entertainment are designed to provide prediction errors, surprise, and provoke, all of which drive engagement. However, a scientist with expertise and passion for a subject will be more engaged in reading the papers related to their field of interest. We form predictions, then seek experiences to test those predictions in nested loops throughout life. We have a certain agency in driving our experience of time through the tasks that we choose to engage with. Given a choice, we choose to engage with tasks that require us to update our memories and form better predictions; being denied a choice can lead to dysfunctions of temporal experiences by becoming either under‐ or overwhelmed with unpredictable change. Engagement, or attention to a task, is a concept that could more formally be described as a sampling of information. The experience of time is fundamentally dependent on the quantity of information, the structure of events, and the records of change within memory. Some studies are starting to tackle this complex notion by adapting lab experiments to real‐life scenarios [67].

The sampling and compression of information between event boundaries determines the rate of compression, which can alter temporal distances. Remembering when depends on the decompression and imperfect reconstruction of information, which may also alter temporal distances. Recent behavioral work has established how the nested structure of events drives temporal distances between items in episodic memory [133]. However, questions remain as to how the compression of information at encoding and the decompression and reconstruction at retrieval each contribute to the temporal distances between memories and the subjective experience of time. Specifically, looking for markers with EEG during both encoding and retrieval of segmented stimuli may provide the clearest answers with evidence of temporal compression and the establishment of temporal tags in memory [136]. We would expect participants to flexibly adapt their strategies for either forward or backward scanning of memory based on the task. Differences in temporal distances depend on the quantity of information within nested event structures and how the to‐be‐remembered information aligns with narrative schema [137].

The construction of memory and the experience of time may depend on temporal integration windows delineated by context shifts, which could be described as packets within oscillatory cycles [138] or presemantic windows [134, 139]. The retrieval of memories involves the creative reconstruction of past events [140, 141], and a study of segmentation has suggested that the basis for reconstruction involves skipping across encoded event boundaries. When asked to retrieve a target item from a particular movie segment, participants’ reaction times to identify an item depended upon the number of boundaries and the distance between the item and the previous boundary [142]. It is important to note that although participants were not required to provide judgments of the passage of time or duration estimates, the time to retrieve the memory for a target item depended upon the number of boundaries and the distance between the target item and the closest boundary.

While segmentation effects can be provided by external contextual shifts, critically, shifts can also be internally generated. Task switching has been shown to influence the experience of time [66] and has also been shown to create boundaries that impair memory for temporal order [143]. Experiencing either externally or internally generated change provides segmentation effects in memory; the construction of episodic memories and the subjective experience of duration may be described in terms of the segmentation of events or a fluctuating contextual drift. However, rather than distinguishing between segmentation and contextual drift, the two theoretical accounts may both be correct. An alternative view is that durations are not stored but events are temporally marked, allowing to compute their distances in time [6, 144]. Crucially, temporal order cannot be explained by internal clock models, whereas a temporal marker account also provides an order with memory for events reaching into the past and imaginatively constructed events reaching into the future.

In summary, in memory research, segmentation parses streams of information into meaningful bits called events and episodes that are hierarchically nested. However, it is essential to dissociate the parsing of information from the parsing of time. If information is segmented or chunked, this does not warrant that the time interval associated with the beginning and the end of the information segment is itself represented [145, 146]. By representation, we mean “a symbolic read‐write memory that carries information extracted from experience forward in time in a computationally accessible form” [6]. Herein, we suggest that salient moments like event boundaries used in memory parsers, which imply contextual change, may be temporally tagged in memory. This time‐tagging operation may be a more parsimonious solution than duration storage for real‐time temporal coding of singular life events. One implication is that long‐term storage of temporal information is not duration but time tags [6, 146]. Context shifts may provide salient markers of time passing by virtue of being privileged moments for coding temporal information. Temporal distances in the event model can be determined by how much contextual change occurs; the compression of information provides an explanation for how retrospective duration tends to be underestimated. The quantity of information experienced between boundaries determines a compression rate. Time estimates require the computation of information; the greater the compression rate, the more time will be underestimated. Attending to time increases the sampling rate (temporal resolution) of information processing (seeing the trees rather than the forest), which alters the compression rate and the subsequent decompression and reconstruction of information when making duration estimates.

7Conclusion

The current article highlights the potential development of unified theories of time and memory. Daily personal experiences are composed of creative constructions of events that are encoded into long‐term memory if sufficient changes occur; similarly, changes influence temporal distance and the subjective experience of time. Studies of time and memory may benefit from converging on the study of fluctuating context drift. The rate of drift may be influenced by one's experience of change, which determines the rate of compression and the contractions and dilations of time in the imperfect reconstruction of memories on the timelines of our lives. Time flows with the changing of events.

Author Contributions

Matthew Logie: conceptualization, writing – original draft, writing – review and editing, visualization. Marianna Lamprou‐Kokolaki: conceptualization, writing – review and editing. Virginie van Wassenhove: conceptualization, writing – review and editing, visualization, supervision, project administration, funding acquisition.

Conflicts of Interest

All authors declare no conflicts of interest

References

1J. M. Zacks , “Event Perception and Memory ,” Annual Review of Psychology
71 (2020 ): 165 –191 , 10.1146/annurev-psych-010419-051101 .PMC8679009 31905113

2R. A. Block , “Contextual Coding in Memory: Studies of Remembered Duration,” in Time, Mind, and Behavior , ed. J. A. Michon and J. L. Jackson (Springer, 1985 ), 169 –178 , 10.1007/978-3-642-70491-8_11 .

3W. D. Poynter , “Duration Judgment and the Segmentation of Experience ,” Memory & Cognition
11 , no. 1 (1983 ): 77 –82 , 10.3758/BF03197664 .6855562

4V. van Wassenhove , “Minding Time in an Amodal Representational Space ,” Philosophical Transactions of the Royal Society B: Biological Sciences
364 , no. 1525 (2009 ): 1815 –1830 , 10.1098/rstb.2009.0023 .PMC2685822 19487185

5V. van Wassenhove , “Defining Moments for Conscious Time and Content ,” PsyCh Journal
6 , no. 2 (2017 ): 168 –169 , 10.1002/pchj.166 .28561997

6C. R. Gallistel , The Organization of Learning (MIT Press, 1990 ), viii , 648.

7L. Azizi , I. Polti , and V. Wassenhove , “Spontaneous α Brain Dynamics Track the Episodic “When” ,” Journal of Neuroscience
43 , no. 43 (2023 ): 7186 –7197 , 10.1523/JNEUROSCI.0816-23.2023 .PMC10601376 37704373

8V. van Wassenhove , “Cracking the Neural Code of How the Brain Represents Time May Make the Dualistic Stance Obsolete ,” Timing & Time Perception
12 , no. 2 (2023 ): 221 –229 , 10.1163/22134468-bja10099 .

9S. Droit‐Volet , W. H. Meck , and T. B. Penney , “Sensory Modality and Time Perception in Children and Adults ,” Behavioural Processes
74 , no. 2 (2007 ): 244 –250 , 10.1016/j.beproc.2006.09.012 .17084041

10H. Lejeune , “Switching or Gating? The Attentional Challenge in Cognitive Models of Psychological Time ,” Behavioural Processes
44 , no. 2 (1998 ): 127 –145 , 10.1016/S0376-6357(98)00045-X .24896971

11T. B. Penney , J. Gibbon , and W. H. Meck , “Differential Effects of Auditory and Visual Signals on Clock Speed and Temporal Memory ,” Journal of Experimental Psychology: Human Perception and Performance
26 , no. 6 (2000 ): 1770 –1787 , 10.1037/0096-1523.26.6.1770 .11129373

12W. D. Poynter and D. Homa , “Duration Judgment and the Experience of Change ,” Perception & Psychophysics
33 , no. 6 (1983 ): 548 –560 , 10.3758/BF03202936 .6622190

13R. M. Church , “Properties of the Internal Clock ,” Annals of the New York Academy of Sciences
423 (1984 ): 566 –582 , 10.1111/j.1749-6632.1984.tb23459.x .6588815

14M. Treisman , “Temporal Discrimination and the Indifference Interval: Implications for a Model of the ‘Internal Clock’ ,” Psychological Monographs: General and Applied
77 , no. 13 (1963 ): 1 –31 , 10.1037/h0093864 .5877542

15C. Miall , “The Storage of Time Intervals Using Oscillating Neurons ,” Neural Computation
1 , no. 3 (1989 ): 359 –371 , 10.1162/neco.1989.1.3.359 .

16M. Treisman , “The Internal Clock and the Structure of Time Perception ,” Procedia—Social and Behavioral Sciences, International Conference on Timing and Time Perception, 31 March – 3 April 2014, Corfu, Greece
126 (2014 ): 3 , 10.1016/j.sbspro.2014.02.295 .

17J. de Jong , E. Akyürek , and H. van Rijn , “A Unified Neurocomputational Model of Prospective and Retrospective Timing ,” Psychological Review
132 , no. 4 (2025 ): 781 –827 , 10.1037/rev0000519 .39760713

18Z. Fountas , A. Sylaidi , K. Nikiforou , A. K. Seth , M. Shanahan , and W. Roseboom , “A Predictive Processing Model of Episodic Memory and Time Perception ,” Neural Computation
34 , no. 7 (2022 ): 1501 –1544 , 10.1162/neco_a_01514 .35671462

19P. A. Lewis and R. C. Miall , “Remembering the Time: A Continuous Clock ,” Trends in Cognitive Sciences
10 , no. 9 (2006 ): 401 –406 , 10.1016/j.tics.2006.07.006 .16899395

20J. E. R. Staddon and J. J. Higa , “Interval Timing ,” Nature Reviews Neuroscience
7 , no. 8 (2006 ): 678 –678 , 10.1038/nrn1764-c1 .

21J. Gibbon , C. Malapani , C. L. Dale , and C. R. Gallistel , “Toward a Neurobiology of Temporal Cognition: Advances and Challenges ,” Current Opinion in Neurobiology
7 , no. 2 (1997 ): 170 –184 , 10.1016/S0959-4388(97)80005-0 .9142762

22U. R. Karmarkar and D. V. Buonomano , “Timing in the Absence of Clocks: Encoding Time in Neural Network States ,” Neuron
53 , no. 3 (2007 ): 427 –438 , 10.1016/j.neuron.2007.01.006 .PMC1857310 17270738

23R. E. Ornstein , On the Experience of Time (Harmondsworth, 1969 ).

24P. Fraisse , “Chapter 6—Time and Rhythm Perception,” in Perceptual Coding , ed. E. C. Carterette and M. P. Friedman (Academic Press, 1978 ), 203 –254 , 10.1016/B978-0-12-161908-4.50012-7 .

25S. K. Herbst , A. H. Javadi , E. Van Der Meer , and N. A. Busch , “How Long Depends on How Fast—Perceived Flicker Dilates Subjective Duration ,” PLoS ONE
8 , no. 10 (2013 ): e76074, 10.1371/journal.pone.0076074 .PMC3806760 24194829

26W. Roseboom , Z. Fountas , K. Nikiforou , D. Bhowmik , M. Shanahan , and A. K. Seth , “Activity in Perceptual Classification Networks as a Basis for Human Subjective Time Perception ,” Nature Communications
10 , no. 1 (2019 ): 267 , 10.1038/s41467-018-08194-7 .PMC6336826 30655543

27C. Y. Jin , A. Razafindrahaba , R. Bordas , and V. Van Wassenhove , “Separating Sensory From Timing Processes: A Cognitive Encoding and Neural Decoding Approach ,” bioRxiv (2024 ), 10.1101/2024.06.24.600536 .

28A. Johnston , D. H. Arnold , and S. Nishida , “Spatially Localized Distortions of Event Time ,” Current Biology
16 , no. 5 (2006 ): 472 –479 , 10.1016/j.cub.2006.01.032 .16527741

29R. A. Block and M. A. Reed , “Remembered Duration: Evidence for a Contextual‐Change Hypothesis ,” Journal of Experimental Psychology: Human Learning and Memory
4 , no. 6 (1978 ): 656 –665 , 10.1037/0278-7393.4.6.656 .

30M. B. Ahrens and M. Sahani , “Observers Exploit Stochastic Models of Sensory Change to Help Judge the Passage of Time ,” Current Biology
21 , no. 3 (2011 ): 200 –206 , 10.1016/j.cub.2010.12.043 .PMC3094759 21256018

31E. Tulving , M. E. Le Voi , D. A. Routh , and E. Loftus , “Ecphoric Processes in Episodic Memory ,” Philosophical Transactions of the Royal Society of London B, Biological Sciences
302 , no. 1110 (1997 ): 361 –371 , 10.1098/rstb.1983.0060 .

32R. Logie , V. Camos , and N. Cowan , Working Memory: The State of the Science (Oxford University Press, 2020 ).

33E. Tulving , “Episodic Memory: From Mind to Brain ,” Annual Review of Psychology
53 , no. 1 (2002 ): 1 –25 , 10.1146/annurev.psych.53.100901.135114 .11752477

34J. Q. Sargent , J. M. Zacks , D. Z. Hambrick , et al., “Event Segmentation Ability Uniquely Predicts Event Memory ,” Cognition
129 , no. 2 (2013 ): 241 –255 , 10.1016/j.cognition.2013.07.002 .PMC3821069 23942350

35L. L. Richmond and J. M. Zacks , “Constructing Experience: Event Models From Perception to Action ,” Trends in Cognitive Sciences
21 , no. 12 (2017 ): 962 –980 , 10.1016/j.tics.2017.08.005 .PMC5694361 28899609

36C. Ye , Q. Liu , and R. H. Logie , “When Repeated Presentation of Visual Feature Bindings Does and Does Not Result in Learning: Visual Short‐Term and Long‐Term Memory Are Distinct but Work in Tandem ,” Memory & Cognition
54 , no. 4 (2026 ): 1388 –1406 , 10.3758/s13421-025-01816-8 .PMC13253647 41318740

37M. Rinck and G. H. Bower , “Temporal and Spatial Distance in Situation Models ,” Memory & Cognition
28 , no. 8 (2000 ): 1310 –1320 , 10.3758/BF03211832 .11219959

38G. Xue , “From Remembering to Reconstruction: The Transformative Neural Representation of Episodic Memory ,” Progress in Neurobiology
219 (2022 ): 102351, 10.1016/j.pneurobio.2022.102351 .36089107

39K. A. Pettijohn , A. N. Thompson , A. K. Tamplin , S. A. Krawietz , and G. A. Radvansky , “Event Boundaries and Memory Improvement ,” Cognition
148 (2016 ): 136 –144 , 10.1016/j.cognition.2015.12.013 .26780472

40K. M. Swallow , J. M. Zacks , and R. A. Abrams , “Event Boundaries in Perception Affect Memory Encoding and Updating ,” Journal of Experimental Psychology: General
138 , no. 2 (2009 ): 236 –257 , 10.1037/a0015631 .PMC2819197 19397382

41Y. S. Shin and S. DuBrow , “Structuring Memory Through Inference‐Based Event Segmentation ,” Topics in Cognitive Science
13 , no. 1 (2021 ): 106 –127 , 10.1111/tops.12505 .32459391

42S. Baror , M. Cohen , N. Haik , G. Avraham , and A. Ben‐Yakov , “The Role of Context in Continuity and Segmentation ,” Nature Human Behaviour
10 (2026 ): 988 –1005 , 10.1038/s41562-026-02403-w .PMC13212156 41673193

43M. R. Logie and D. I. Donaldson , “Do Doorways Really Matter: Investigating Memory Benefits of Event Segmentation in a Virtual Learning Environment ,” Cognition
209 (2021 ): 104578, 10.1016/j.cognition.2020.104578 .33422863

44B. Güler , F. Serin , and E. Günseli , “Prediction Error Is Out of Context: The Dominance of Contextual Stability in Structuring Episodic Memories ,” Psychonomic Bulletin & Review
32 , no. 6 (2025 ): 2957 –2968 , 10.3758/s13423-025-02723-4 .PMC12627157 40571834

45J. M. Zacks , N. K. Speer , K. M. Swallow , T. S. Braver , and J. R. Reynolds , “Event Perception: A Mind‐Brain Perspective ,” Psychological Bulletin
133 , no. 2 (2007 ): 273 –293 , 10.1037/0033-2909.133.2.273 .PMC2852534 17338600

46C. Baldassano , J. Chen , A. Zadbood , J. W. Pillow , U. Hasson , and K. A. Norman , “Discovering Event Structure in Continuous Narrative Perception and Memory ,” Neuron
95 , no. 3 (2017 ): 709 –721.e5 , 10.1016/j.neuron.2017.06.041 .PMC5558154 28772125

47J. M. Zacks and B. Tversky , “Event Structure in Perception and Conception ,” Psychological Bulletin
127 , no. 1 (2001 ): 3 –21 , 10.1037/0033-2909.127.1.3 .11271755

48V. Pariyadath and D. Eagleman , “The Effect of Predictability on Subjective Duration ,” PLoS ONE
2 , no. 11 (2007 ): e1264, 10.1371/journal.pone.0001264 .PMC2082074 18043760

49D. Rose and J. Summers , “Duration Illusions in a Train of Visual Stimuli ,” Perception
24 , no. 10 (1995 ): 1177 –1187 , 10.1068/p241177 .8577576

50P. U. Tse , J. Intriligator , J. Rivest , and P. Cavanagh , “Attention and the Subjective Expansion of Time ,” Perception & Psychophysics
66 , no. 7 (2004 ): 1171 –1189 , 10.3758/bf03196844 .15751474

51K. E. Mathewson , M. Fabiani , G. Gratton , D. M. Beck , and A. Lleras , “Rescuing Stimuli From Invisibility: Inducing a Momentary Release From Visual Masking With Pre‐Target Entrainment ,” Cognition
115 , no. 1 (2010 ): 186 –191 , 10.1016/j.cognition.2009.11.010 .20035933

52M. R. Jones , H. Moynihan , N. MacKenzie , and J. Puente , “Temporal Aspects of Stimulus‐Driven Attending in Dynamic Arrays ,” Psychological Science
13 , no. 4 (2002 ): 313 –319 , 10.1111/1467-9280.00458 .12137133

53V. Wassenhove , D. V. Buonomano , S. Shimojo , and L. Shams , “Distortions of Subjective Time Perception Within and Across Senses ,” PLoS ONE
3 , no. 1 (2008 ): e1437, 10.1371/journal.pone.0001437 .PMC2174530 18197248

54D. Linares and A. Gorea , “Temporal Frequency of Events Rather Than Speed Dilates Perceived Duration of Moving Objects ,” Scientific Reports
5 , no. 1 (2015 ): 8825, 10.1038/srep08825 .PMC4351521 25744877

55M. C. Morrone , J. Ross , and D. Burr , “Saccadic Eye Movements Cause Compression of Time as Well as Space ,” Nature Neuroscience
8 , no. 7 (2005 ): 950 –954 , 10.1038/nn1488 .15965472

56I. K. Brunec , J. D. Ozubko , T. Ander , R. Guo , M. Moscovitch , and M. D. Barense , “Turns During Navigation Act as Boundaries That Enhance Spatial Memory and Expand Time Estimation ,” Neuropsychologia
141 (2020 ): 107437, 10.1016/j.neuropsychologia.2020.107437 .32171736

57A. J. Horner , J. A. Bisby , A. Wang , K. Bogus , and N. Burgess , “The Role of Spatial Boundaries in Shaping Long‐Term Event Representations ,” Cognition
154 (2016 ): 151 –164 , 10.1016/j.cognition.2016.05.013 .PMC4955252 27295330

58M. R. Jones and M. Boltz , “Dynamic Attending and Responses to Time ,” Psychological Review
96 , no. 3 (1989 ): 459 –491 , 10.1037/0033-295X.96.3.459 .2756068

59H.‐Y. S. Chien and C. J. Honey , “Constructing and Forgetting Temporal Context in the Human Cerebral Cortex ,” Neuron
106 , no. 4 (2020 ): 675 –686.e11 , 10.1016/j.neuron.2020.02.013 .PMC7244383 32164874

60C. J. Honey , “Temporal Hierarchies in Human Cerebral Cortex ,” Journal of Vision
18 , no. 10 (2018 ): 1372, 10.1167/18.10.1372 .

61M. McClay , M. E. Sachs , and D. Clewett , “Dynamic Emotional States Shape the Episodic Structure of Memory ,” Nature Communications
14 , no. 1 (2023 ): 6533 , 10.1038/s41467-023-42241-2 .PMC10582075 37848429

62T. M. Tomita , M. D. Barense , and C. J. Honey , The Similarity Structure of Real‐World Memories (2021 ) bioRxiv, 10.1101/2021.01.28.428278 .

63D. Talmi and D. J. Palombo , “Emotional Time Travel: The Role of Emotion in Temporal Memory ,” Cognition and Emotion
39 , no. 1 (2025 ): 1 –17 , 10.1080/02699931.2024.2421395 .40009765

64C. R. Gallistel and J. Gibbon , “Time, Rate, and Conditioning ,” Psychological Review
107 , no. 2 (2000 ): 289 –344 , 10.1037/0033-295X.107.2.289 .10789198

65D. Poynter , “Chapter 8 Judging the Duration of Time Intervals: A Process of Remembering Segments of Experience,” in Advances in Psychology , ed. I. Levin and D. Zakay (North‐Holland, 1989 ), Vol. 59 , pp. 305 –331 , 10.1016/S0166-4115(08)61045-6 .

66S. Xu and P. David , “Distortions in Time Perceptions During Task Switching ,” Computers in Human Behavior
80 (2018 ): 362 –369 , 10.1016/j.chb.2017.11.032 .

67J.‐M. Josset , E. Le Quentrec , and V. van Wassenhove , “Our Sweetest Hours Fly Fastest…on Smartphone ,” Proceedings of the Annual Meeting of the Cognitive Science Society
46 (2024 ), https://escholarship.org/uc/item/3b92z1b9.

68R. S. Ogden , E. Salominaite , L. A. Jones , J. E. Fisk , and C. Montgomery , “The Role of Executive Functions in Human Prospective Interval Timing ,” Acta Psychologica
137 , no. 3 (2011 ): 352 –358 , 10.1016/j.actpsy.2011.04.004 .21561595

69R. A. Block and D. Zakay , “Prospective and Retrospective Duration Judgments: A Meta‐Analytic Review ,” Psychonomic Bulletin & Review
4 , no. 2 (1997 ): 184 –197 , 10.3758/BF03209393 .21331825

70D. Zakay and R. Block , “Prospective and Retrospective Duration Judgments: An Executive‐Control Perspective ,” Acta Neurobiologiae Experimentalis
64 , no. 3 (2004 ): 3 , 10.55782/ane-2004-1516 .15283475

71A. Mehrabian , “Individual Differences in Stimulus Screening and Arousability ,” Journal of Personality
45 , no. 2 (1977 ): 237 –250 , 10.1111/j.1467-6494.1977.tb00149.x .881637

72D. Zakay , “Psychological Time as Information: The Case of Boredom† ,” Frontiers in Psychology
5 (2014 ): 917, 10.3389/fpsyg.2014.00917 .PMC4140165 25191296

73J. McFadyen , C. Nolan , E. Pinocy , D. Buteri , and O. Baumann , “Doorways Do Not Always Cause Forgetting: A Multimodal Investigation ,” BMC Psychology
9 , no. 1 (2021 ): 41 , 10.1186/s40359-021-00536-3 .PMC7938580 33685514

74D. van Helvoort , E. Stobbe , R. Benning , H. Otgaar , and V. van de Ven , “Physical Exploration of a Virtual Reality Environment: Effects on Spatiotemporal Associative Recognition of Episodic Memory ,” Memory & Cognition
48 , no. 5 (2020 ): 691 –703 , 10.3758/s13421-020-01024-6 .PMC7320060 32103427

75W. Roseboom , A. Seth , M. T. Sherman , and Z. Fountas , The Perception of Time in Humans, Brains, and Machines (2022 ), 10.31234/osf.io/c7vzx .

76K. C. Mukherjee , “Vierordt's Law ,” British Journal of Psychology General Section
21 , no. 3 (1931 ): 326 –328 , 10.1111/j.2044-8295.1931.tb00594.x .

77M. H. Herzog , L. Drissi‐Daoudi , and A. Doerig , “All in Good Time: Long‐Lasting Postdictive Effects Reveal Discrete Perception ,” Trends in Cognitive Sciences
24 , no. 10 (2020 ): 826 –837 , 10.1016/j.tics.2020.07.001 .32893140

78R. VanRullen and C. Koch , “Is Perception Discrete or Continuous? ,” Trends in Cognitive Sciences
7 , no. 5 (2003 ): 207 –213 , 10.1016/S1364-6613(03)00095-0 .12757822

79M. W. Howard and M. J. Kahana , “A Distributed Representation of Temporal Context ,” Journal of Mathematical Psychology
46 , no. 3 (2002 ): 269 –299 , 10.1006/jmps.2001.1388 .

80S. DuBrow , N. Rouhani , Y. Niv , and K. A. Norman , “Does Mental Context Drift or Shift? ,” Current Opinion in Behavioral Sciences
17 (2017 ): 141 –146 , 10.1016/j.cobeha.2017.08.003 .PMC5766042 29335678

81Y. Pu , X.‐Z. Kong , C. Ranganath , and L. Melloni , “Event Boundaries Shape Temporal Organization of Memory by Resetting Temporal Context ,” Nature Communications
13 , no. 1 (2022 ): 622 , 10.1038/s41467-022-28216-9 .PMC8810807 35110527

82J. R. Manning , S. M. Polyn , G. H. Baltuch , B. Litt , and M. J. Kahana , “Oscillatory Patterns in Temporal Lobe Reveal Context Reinstatement During Memory Search ,” Proceedings of the National Academy of Sciences
108 , no. 31 (2011 ): 12893 –12897 , 10.1073/pnas.1015174108 .PMC3150951 21737744

83L. Postman , “Organization and Interference ,” Psychological Review
78 , no. 4 (1971 ): 290 –302 , 10.1037/h0031031 .

84N. K. Speer and J. M. Zacks , “Temporal Changes as Event Boundaries: Processing and Memory Consequences of Narrative Time Shifts☆ ,” Journal of Memory and Language
53 , no. 1 (2005 ): 125 –140 , 10.1016/j.jml.2005.02.009 .

85S. DuBrow and L. Davachi , “Temporal Memory Is Shaped by Encoding Stability and Intervening Item Reactivation ,” Journal of Neuroscience
34 , no. 42 (2014 ): 13998 –14005 , 10.1523/JNEUROSCI.2535-14.2014 .PMC4198540 25319696

86S. DuBrow and L. Davachi , “Temporal Binding Within and Across Events ,” Neurobiology of Learning and Memory
134 (2016 ): 107 –114 , 10.1016/j.nlm.2016.07.011 .PMC5018468 27422018

87Y. Ezzyat and L. Davachi , “Similarity Breeds Proximity: Pattern Similarity Within and Across Contexts Is Related to Later Mnemonic Judgments of Temporal Proximity ,” Neuron
81 , no. 5 (2014 ): 1179 –1189 , 10.1016/j.neuron.2014.01.042 .PMC3983791 24607235

88L. J. Lohnas , M. K. Healey , and L. Davachi , “Neural Temporal Context Reinstatement of Event Structure During Memory Recall ” Journal of Experimental Psychology: General
152 , no. 7 (2023 ): 1840 –1872 , 10.1037/xge0001354 .PMC10293072 37036669

89B. R. Kanter , C. M. Lykken , I. Polti , M.‐B. Moser , and E. I. Moser , “Event Structure Sculpts Neural Population Dynamics in the Lateral Entorhinal Cortex ,” Science
388 , no. 6754 (2025 ): eadr0927, 10.1126/science.adr0927 .40570128

90J. Wang , A. Tambini , L. Pritschet , C. M. Taylor , E. G. Jacobs , and R. C. Lapate , “The Intrinsic Time Tracker: Temporal Context Is Embedded in Entorhinal and Hippocampal Functional Connectivity Patterns ,” Nature Communications
16 , no. 1 (2025 ): 8817 , 10.1038/s41467-025-63633-6 .PMC12494713 41044064

91V. van Wassenhove , B. R. Kanter , S. Viganò , and R. Bordas , “A Passage of Time Signal in the Human Brain ,” eNeuro
13 , no. 1 (2026 ), 10.1523/ENEURO.0406-25.2025 .PMC12826127 41565467

92C. Fenerci , K. da Silva Castanheira , M. LoParco , and S. Sheldon , “Changes in the Experience of Time: The Impact of Spatial Information on the Perception and Memory of Duration ,” Quarterly Journal of Experimental Psychology
74 , no. 3 (2021 ): 471 –482 , 10.1177/1747021820968492 .33124961

93E. E. Davis and K. L. Campbell , “Event Boundaries Structure the Contents of Long‐Term Memory in Younger and Older Adults ,” Memory
31 , no. 1 (2023 ): 47 –60 , 10.1080/09658211.2022.2122998 .36107809

94C. A. Kurby and J. M. Zacks , “Segmentation in the Perception and Memory of Events ,” Trends in Cognitive Sciences
12 , no. 2 (2008 ): 72 –79 , 10.1016/j.tics.2007.11.004 .PMC2263140 18178125

95R. Masís‐Obando , K. A. Norman , and C. Baldassano , “Spatial Contexts With Reliable Neural Representations Support Reinstatement of Subsequently Placed Objects ,” Nature Human Behaviour
10 , no. 1 (2026 ): 164 –181 , 10.1038/s41562-025-02379-z .PMC12846921 41482597

96C. Wen , S. R. Yousif , and B. E. Sherman , “Unfolding Event Structure Distorts Subjective Time ,” Cognition
267 (2026 ): 106354, 10.1016/j.cognition.2025.106354 .41166803

97M. R. Logie and D. I. Donaldson , “Optimising Episodic Encoding Within Segmented Virtual Contexts ,” Consciousness and Cognition
128 (2025 ): 103807, 10.1016/j.concog.2024.103807 .39756357

98C. Colson , G. Panneels , and A. D'Argembeau , “Negative Emotion Reduces the Temporal Compression of Events in Episodic Memory ,” Cognition and Emotion
40 , no. 2 (2026 ): 271 –286 , 10.1080/02699931.2025.2501047 .40340765

99Z. C. Chao , D. G. Dillon , Y.‐H. Liu , E. M. Barrick , and C.‐T. Wu , “Altered Coordination Between Frontal Delta and Parietal Alpha Networks Underlies Anhedonia and Depressive Rumination in Major Depressive Disorder ,” Journal of Psychiatry and Neuroscience
47 , no. 6 (2022 ): E367 –E378 , 10.1503/jpn.220046 .PMC9633055 36318983

100Z. Dai , H. Zhou , W. Zhang , et al., “Alpha‐Beta Decoupling Relevant to Inhibition Deficits Leads to Suicide Attempt in Major Depressive Disorder ,” Journal of Affective Disorders
314 (2022 ): 168 –175 , 10.1016/j.jad.2022.07.010 .35820473

101A. Strube and D. A. Pizzagalli , “Brain Rhythms of Depression: A Predictive Processing Perspective ,” Trends in Neurosciences
49 , no. 8 (2026 ): 665 –681 , 10.1016/j.tins.2026.06.006 .PMC13344164 42409678

102M. Lamprou Kokolaki and V. Van Wassenhove , “Memorability Shapes the Temporal Structure of Memory ,” (2026 ), 10.2139/ssrn.6997360 .

103G. Buzsáki and D. Tingley , “Space and Time: The Hippocampus as a Sequence Generator ,” Trends in Cognitive Sciences
22 , no. 10 (2018 ): 853 –869 , 10.1016/j.tics.2018.07.006 .PMC6166479 30266146

104P. M. Bays , “Spikes Not Slots: Noise in Neural Populations Limits Working Memory ,” Trends in Cognitive Sciences
19 , no. 8 (2015 ): 431 –438 , 10.1016/j.tics.2015.06.004 .26160026

105S. Planton , T. Van Kerkoerle , L. Abbih , et al., “A Theory of Memory for Binary Sequences: Evidence for a Mental Compression Algorithm in Humans ,” PLOS Computational Biology
17 , no. 1 (2021 ): e1008598, 10.1371/journal.pcbi.1008598 .PMC7845997 33465081

106H. Lee and J. Chen , “Predicting Memory From the Network Structure of Naturalistic Events ,” Nature Communications
13 , no. 1 (2022 ): 4235 , 10.1038/s41467-022-31965-2 .PMC9307577 35869083

107A. Baddeley , “The Episodic Buffer: A New Component of Working Memory? ,” Trends in Cognitive Sciences
4 , no. 11 (2000 ): 417 –423 , 10.1016/S1364-6613(00)01538-2 .11058819

108R. J. Allen , A. D. Baddeley , and G. J. Hitch , “Awareness as the Heart of Working Memory ,” Trends in Cognitive Sciences (2026 ), Advance online publication. 10.1016/j.tics.2026.04.001 .42034504

109N. Leroy , S. Majerus , and A. D'Argembeau , “Working Memory Capacity for Continuous Events: The Root of Temporal Compression in Episodic Memory? ,” Cognition
247 (2024 ): 105789, 10.1016/j.cognition.2024.105789 .38583322

110N. Leroy and A. D'Argembeau , “The Role of Event Number and Duration in Time‐Compressed Memory Replay ,” Open Mind
9 (2025 ): 2066 –2091 , 10.1162/OPMI.a.276 .PMC12768557 41497529

111G. A. Radvansky , A. C. Doolen , K. A. Pettijohn , and M. Ritchey , “A New Look at Memory Retention and Forgetting ,” Journal of Experimental Psychology: Learning, Memory, and Cognition
48 , no. 11 (2022 ): 1698 –1723 , 10.1037/xlm0001110 .35084927

112N. Leroy , S. Majerus , and A. D'Argembeau , “The Role of Working Memory Capacity in the Temporal Compression of Episodic Memories: An Individual Differences Approach ,” Journal of Experimental Psychology: Learning, Memory, and Cognition
51 , no. 2 (2025 ): 285 –300 , 10.1037/xlm0001350 .38913729

113M. Kumar , A. Goldstein , S. Michelmann , J. M. Zacks , U. Hasson , and K. A. Norman , “Bayesian Surprise Predicts Human Event Segmentation in Story Listening ,” Cognitive Science
47 , no. 10 (2023 ): e13343, 10.1111/cogs.13343 .PMC11654724 37867379

114K. J. Jeffery and C. Rovelli , “Transitions in Brain Evolution: Space, Time and Entropy ,” Trends in Neurosciences
43 , no. 7 (2020 ): 467 –474 , 10.1016/j.tins.2020.04.008 .PMC7183980 32414530

115J. Gibbon , R. M. Church , and W. H. Meck , “Scalar Timing in Memory ,” Annals of the New York Academy of Sciences
423 (1984 ): 52 –77 , 10.1111/j.1749-6632.1984.tb23417.x .6588812

116J. Gibbon , “Scalar Expectancy Theory and Weber's Law in Animal Timing ,” Psychological Review
84 , no. 3 (1977 ): 279 –325 , 10.1037/0033-295X.84.3.279 .

117C. V. Buhusi and W. H. Meck , “Relative Time Sharing: New Findings and an Extension of the Resource Allocation Model of Temporal Processing ,” Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
364 , no. 1525 (2009 ): 1875 –1885 , 10.1098/rstb.2009.0022 .PMC2685821 19487190

118C. Lustig and W. H. Meck , “Modality Differences in Timing and Temporal Memory Throughout the Lifespan ,” Brain and Cognition
77 , no. 2 (2011 ): 298 –303 , 10.1016/j.bandc.2011.07.007 .21843912

119J. M. Salet , J. de Jong , and H. van Rijn , “Still Stuck With the Stopwatch ,” Behavioral Neuroscience
136 , no. 5 (2022 ): 453 –466 , 10.1037/bne0000527 .36222638

120A. Baddeley , “The Fractionation of Working Memory ,” Proceedings of the National Academy of Sciences
93 , no. 24 (1996 ): 13468 –13472 , 10.1073/pnas.93.24.13468 .PMC33632 8942958

121D. Dennett and M. Kinsbourne , “Multiple Drafts: An Eternal Golden Braid? ,” Behavioral and Brain Sciences
18 , no. 4 (1995 ): 810 –811 , 10.1017/S0140525x00041121 .

122R. H. Logie , “Retiring the Central Executive ,” Quarterly Journal of Experimental Psychology
69 , no. 10 (2016 ): 2093 –2109 , 10.1080/17470218.2015.1136657 .26821744

123R. C. O'Reilly , T. E. Hazy , and S. A. Herd , “The Leabra Cognitive Architecture: How to Play 20 Principles With Nature and Win!,” in The Oxford Handbook of Cognitive Science (Oxford University Press, 2017 ), 91 –115 .

124A. Barri , M. T. Wiechert , M. Jazayeri , and D. A. DiGregorio , “Synaptic Basis of a Sub‐Second Representation of Time in a Neural Circuit Model ,” Nature Communications
13 , no. 1 (2022 ): 7902 , 10.1038/s41467-022-35395-y .PMC9780315 36550115

125M. Jazayeri and M. N. Shadlen , “Temporal Context Calibrates Interval Timing ,” Nature Neuroscience
13 , no. 8 (2010 ): 1020 –1026 , 10.1038/nn.2590 .PMC2916084 20581842

126M. Chaumon , P.‐A. Rioux , S. K. Herbst , et al., “The Blursday Database as a Resource to Study Subjective Temporalities During COVID‐19 ,” Nature Human Behaviour
6 , no. 11 (2022 ): 1587 –1599 , 10.1038/s41562-022-01419-2 .35970902

127Ş. L. Runyun , V. Van Wassenhove , and F. Balci , “Altered Temporal Awareness During Covid‐19 Pandemic ,” Psychological Research
88 , no. 8 (2024 ): 2335 –2345 , 10.1007/s00426-024-02004-0 .39034344

128S. K. Herbst , I. Mangione , T. W. Kononowicz , Y. Shen , and V. Van Wassenhove , “Abstracting Time in Memory ,” Journal of Experimental Psychology: Learning, Memory, and Cognition
51 , no. 10 (2025 ): 1576 –1593 , 10.1037/xlm0001449 .39977685

129S. K. Herbst , I. Mangione , C.‐R. Segerie , et al., “Alpha Power Indexes Working Memory Load for Durations ,” Iscience
29 , no. 1 (2026 ): 114212, 10.1016/j.isci.2025.114212 .PMC12757647 41488787

130M. Jording , D. H. V. Vogel , S. Viswanathan , and K. Vogeley , “Dissociating Passage and Duration of Time Experiences Through the Intensity of Ongoing Visual Change ,” Scientific Reports
12 , no. 1 (2022 ): 8226 , 10.1038/s41598-022-12063-1 .PMC9113985 35581249

131M. Lamprou‐Kokolaki , Y. Nédélec , S. Lhuillier , and V. van Wassenhove , “Distinctive Features of Experiential Time: Duration, Speed and Event Density ,” Consciousness and Cognition
118 (2024 ): 103635, 10.1016/j.concog.2024.103635 .38219402

132I. Polti , B. Martin , and V. van Wassenhove , “The Effect of Attention and Working Memory on the Estimation of Elapsed Time ,” Scientific Reports
8 , no. 1 (2018 ): 6690 , 10.1038/s41598-018-25119-y .PMC5923266 29703928

133M. Logie , C. Grasso , and V. van Wassenhove , “Nested Contextual Change and the Temporal Compression of Episodic Memory ,” Scientific Reports
16 (2026 ): 33698, 10.1038/s41598-026-64037-2 .

134E. Pöppel , “Pre‐Semantically Defined Temporal Windows for Cognitive Processing ,” Philosophical Transactions of the Royal Society B: Biological Sciences
364 , no. 1525 (2009 ): 1887 –1896 , 10.1098/rstb.2009.0015 .PMC2685817 19487191

135O. Jeunehomme , N. Leroy , and A. D'Argembeau , “The Temporal Compression of Events During Episodic Future Thinking ,” Cognition
205 (2020 ): 104416, 10.1016/j.cognition.2020.104416 .32773151

136M. Silva , X. Wu , and L. Fuentemilla , “Neural Reactivation Supports Memory Formation When Events End ,” Trends in Cognitive Sciences (2026 ), 10.1016/j.tics.2026.07.002 .42586904

137J. P. Cockcroft , S. C. Berens , M. G. Gaskell , and A. J. Horner , “Schematic Information Influences Memory and Generalisation Behaviour for Schema‐Relevant and ‐Irrelevant Information ,” Cognition
227 (2022 ): 105203, 10.1016/j.cognition.2022.105203 .35717767

138E. K. Miller , “The “Working” of Working Memory ,” Dialogues in Clinical Neuroscience
15 , no. 4 (2013 ): 411 –418 , 10.31887/DCNS.2013.15.4/emiller .PMC3898679 24459408

139E. Pöppel , “Time Perception,” in Perception , ed. S. M. Anstis , J. Atkinson , C. Blakemore , O. Braddick , T. Brandt , F. W. Campbell , S. Coren , J. Dichgans , P. C. Dodwell , P. D. Eimas , J. M. Foley , R. Fox , L. Ganz , M. Garrett , E. J. Gibson , J. S. Girgus , M. M. Haith , Y. Hatwell , E. R. Hilgard , and R. K. Yin , (Springer Berlin Heidelberg, 1978 ), 713 –729 , 10.1007/978-3-642-46354-9_23 .

140D. L. Schacter , “Adaptive Constructive Processes and the Future of Memory ,” American Psychologist
67 , no. 8 (2012 ): 603 –613 , 10.1037/a0029869 .PMC3815569 23163437

141D. L. Schacter , D. R. Addis , and R. L. Buckner , “Episodic Simulation of Future Events ,” Annals of the New York Academy of Sciences
1124 , no. 1 (2008 ): 39 –60 , 10.1196/annals.1440.001 .18400923

142S. Michelmann , U. Hasson , and K. A. Norman , “Evidence That Event Boundaries Are Access Points for Memory Retrieval ,” Psychological Science
34 , no. 3 (2023 ): 326 –344 , 10.1177/09567976221128206 .PMC10152118 36595492

143Y. C. Wang and T. Egner , “Switching Task Sets Creates Event Boundaries in Memory ,” Cognition
221 (2022 ): 104992, 10.1016/j.cognition.2021.104992 .34929522

144W. J. Friedman , “The Development of Temporal Metamemory ,” Child Development
78 , no. 5 (2007 ): 1472 –1491 , 10.1111/j.1467-8624.2007.01078.x .17883443

145R. Jertberg , S. Soto‐Faraco , V. van Wassenhove , and E. van der Burg , Temporal Window of Integration XOR Temporal Window of Synchrony (2025 ), 10.31234/osf.io/8m259_v1 .41173026

146V. van Wassenhove , Cognitive Neuroscience of Time: Nows, Timelines, and Chronologies (2022 ), 10.31234/osf.io/8m9hs .

Come citare questo studio

Matthew Logie, Marianna Lamprou-Kokolaki, Virginie van Wassenhove. (2026). Time Flows With the Changing of Events.. Annals of the New York Academy of Sciences. DOI: 10.1111/nyas.70446

Consulta la pubblicazione originale ↗