Velocity memory

It is known that primates are sensitive to the velocity of moving objects. We can also remember velocity information after moving objects disappear. This cognitive faculty has been investigated before, however, the literature on velocity memory to date has been fragmented. For example, velocity memory has been disparately described as a system that controls eye movements and delayed discrimination. Furthermore, velocity memory may have a role in motion extrapolation, i.e. the ability to judge the position of a moving target after it becomes occluded. This thesis provides a unifying account of velocity memory, and uses electroencephalography (EEG) to explore its neural basis. In Chapter 2, the relationship between oculomotor control and motion extrapolation was investigated. Two forms of motion extrapolation task were presented. In the first, participants observed a moving target disappear then reappear further along its path. Reappearance could be at the correct time, too early or too late. Participants discriminated reappearance error with a two-alternative forced choice button press. In the second task, participants saw identical targets travel behind a visible occluder, and they attempted to press a button at the exact time that it reached the other side. Tasks were completed under fixation and free viewing conditions. The accuracy of participant's judgments was reduced by fixation in both tasks. In addition, eye movements were systematically related to behavioural responses, and small eye movements during fixation were affected by occluded motion. These three results imply that common velocity memory and pre-motor systems mediate eye movements and motion extrapolation. In Chapter 3, different types of velocity representation were explored. Another motion extrapolation task was presented, and targets of a particular colour were associated with fast or slow motion. On identical-velocity probe trials, colour still influenced response times. This indicates that long-term colour-velocity associations influence motion extrapolation. In Chapter 4, interference between subsequently encoded velocities was explored. There was robust interference between motion extrapolation and delayed discrimination tasks, suggesting that common processes are involved in both. In Chapter 5, EEG was used to investigate when memory-guided tracking begins during motion extrapolation. This study compared conditions where participants covertly tracked visible and occluded targets. It was found that a specific event related potential (ERP) appeared around 200 ms post occlusion, irrespective of target location or velocity. This component could delineate the onset of memory guided tracking during occlusion. Finally, Chapter 6 presents evidence that a change in alpha band activity is associated with information processing during motion extrapolation tasks. In light of these results, it is concluded that a common velocity memory system is involved a variety of tasks. In the general discussion (Chapter 7), a new account of velocity memory is proposed. It is suggested that a velocity memory reflects persistent synchronization across several velocity sensitive neural populations after stimulus offset. This distributed network is involved in sensory-motor integration, and can remain active without visual input. Theoretical work on eye movements, delayed discrimination and motion extrapolation could benefit from this account of velocity memory.EThOS - Electronic Theses Online ServiceGBUnited Kingdo

Velocity memory

It is known that primates are sensitive to the velocity of moving objects. We can also remember velocity information after moving objects disappear. This cognitive faculty has been investigated before, however, the literature on velocity memory to date has been fragmented. For example, velocity memory has been disparately described as a system that controls eye movements and delayed discrimination. Furthermore, velocity memory may have a role in motion extrapolation, i.e. the ability to judge the position of a moving target after it becomes occluded. This thesis provides a unifying account of velocity memory, and uses electroencephalography (EEG) to explore its neural basis. In Chapter 2, the relationship between oculomotor control and motion extrapolation was investigated. Two forms of motion extrapolation task were presented. In the first, participants observed a moving target disappear then reappear further along its path. Reappearance could be at the correct time, too early or too late. Participants discriminated reappearance error with a two-alternative forced choice button press. In the second task, participants saw identical targets travel behind a visible occluder, and they attempted to press a button at the exact time that it reached the other side. Tasks were completed under fixation and free viewing conditions. The accuracy of participant's judgments was reduced by fixation in both tasks. In addition, eye movements were systematically related to behavioural responses, and small eye movements during fixation were affected by occluded motion. These three results imply that common velocity memory and pre-motor systems mediate eye movements and motion extrapolation. In Chapter 3, different types of velocity representation were explored. Another motion extrapolation task was presented, and targets of a particular colour were associated with fast or slow motion. On identical-velocity probe trials, colour still influenced response times. This indicates that long-term colour-velocity associations influence motion extrapolation. In Chapter 4, interference between subsequently encoded velocities was explored. There was robust interference between motion extrapolation and delayed discrimination tasks, suggesting that common processes are involved in both. In Chapter 5, EEG was used to investigate when memory-guided tracking begins during motion extrapolation. This study compared conditions where participants covertly tracked visible and occluded targets. It was found that a specific event related potential (ERP) appeared around 200 ms post occlusion, irrespective of target location or velocity. This component could delineate the onset of memory guided tracking during occlusion. Finally, Chapter 6 presents evidence that a change in alpha band activity is associated with information processing during motion extrapolation tasks. In light of these results, it is concluded that a common velocity memory system is involved a variety of tasks. In the general discussion (Chapter 7), a new account of velocity memory is proposed. It is suggested that a velocity memory reflects persistent synchronization across several velocity sensitive neural populations after stimulus offset. This distributed network is involved in sensory-motor integration, and can remain active without visual input. Theoretical work on eye movements, delayed discrimination and motion extrapolation could benefit from this account of velocity memory.EThOS - Electronic Theses Online ServiceGBUnited Kingdo

Increasing frailty is associated with higher prevalence and reduced recognition of delirium in older hospitalised inpatients: results of a multi-centre study

Purpose: Delirium is a neuropsychiatric disorder delineated by an acute change in cognition, attention, and consciousness. It is common, particularly in older adults, but poorly recognised. Frailty is the accumulation of deficits conferring an increased risk of adverse outcomes. We set out to determine how severity of frailty, as measured using the CFS, affected delirium rates, and recognition in hospitalised older people in the United Kingdom. Methods: Adults over 65 years were included in an observational multi-centre audit across UK hospitals, two prospective rounds, and one retrospective note review. Clinical Frailty Scale (CFS), delirium status, and 30-day outcomes were recorded. Results: The overall prevalence of delirium was 16.3% (483). Patients with delirium were more frail than patients without delirium (median CFS 6 vs 4). The risk of delirium was greater with increasing frailty [OR 2.9 (1.8–4.6) in CFS 4 vs 1–3; OR 12.4 (6.2–24.5) in CFS 8 vs 1–3]. Higher CFS was associated with reduced recognition of delirium (OR of 0.7 (0.3–1.9) in CFS 4 compared to 0.2 (0.1–0.7) in CFS 8). These risks were both independent of age and dementia. Conclusion: We have demonstrated an incremental increase in risk of delirium with increasing frailty. This has important clinical implications, suggesting that frailty may provide a more nuanced measure of vulnerability to delirium and poor outcomes. However, the most frail patients are least likely to have their delirium diagnosed and there is a significant lack of research into the underlying pathophysiology of both of these common geriatric syndromes

Simultaneous dynamic mental simulations in physical space and number space

We tested whether there were any dual task costs to running dynamic mental simulations in physical space and number space simultaneously

Liverpool ReproducibiliTEA talks

This is an online repository of slides from at our Liverpool ReproducibiliTEA workshop series. ReproducibilitTEA is an international journal club network designed to raise consciousness about cumulative science and fight the replication crisis. https://reproducibilitea.or

The gap between aesthetic science and aesthetic experience

For over a century we have attempted to understand human aesthetic experience using scientific methods. A typical experiment could be described as reductive and quasi-psychophysical. We vary some aspect of the stimulus and systematically measure some aspect of the aesthetic response. The limitations of this approach can be categorized as problems on the Y axis (what we measure) and the X axis (what we manipulate). The most enigmatic components of aesthetic experience include inclination to cry, aesthetic rapture, a sense of the sublime and intense fascination. However, we cannot evoke these hot aesthetic emotions in the lab, at least not with well controlled stimuli on multiple trials. We thus resort to measuring cold, cognitive preference ratings. There are also problems on the X axis. The reductive psychophysical approach explicitly assumes that there are lawful relations between different stimulus dimensions and preferences. It also tacitly assumes that these dimensions are independent and orthogonal. The second assumption is implausible. Whatever stimulus-preference laws we discover are likely to be twisted and modulated when another dimension is added to the stimuli. This ‘gestalt nightmare’ has long been recognized, but never resolved. This matters, because human aesthetic faculties are probably tuned to the balance and relationship of parts which make up a whole and are indifferent to the parts presented in isolation. I conclude that the future of scientific aesthetics depends on how successfully we can transcend reductive, quasi psychophysical approach. This paper was published in Journal of consciousness studies. Readers may be interested in a counter response from Skov and Nadal (2019), who opposed many of the conclusions. References Makin, A. D. J. (2017). The Gap Between Aesthetic Science and Aesthetic Experience. Journal of Consciousness Studies, 24, 184–213. http://www.ingentaconnect.com/contentone/imp/jcs/2017/00000024/F0020001/art00008 Skov, M., & Nadal, M. (2019). The Nature of Perception and Emotion in Aesthetic Appreciation: A Response to Makin’s Challenge to Empirical Aesthetics. Psychology of Aesthetics, Creativity, and the Arts, 15(3), 470–483. https://doi.org/10.1037/aca000027

A gaze-driven evolutionary algorithm to study aesthetic evaluation of visual symmetry (i-Perception 2016)

Makin, A.J.D., & Bertamini, M., Jones, A., Holmes, T., & Zanker, J. (2016). A gaze-driven evolutionary algorithm to study aesthetic evaluation of visual symmetry i-Perception, 7, 2