Sleep is known to be crucial for human memory, but what about dreams? Previous research has shown that the content of dreams can be manipulated by specific stimuli or tasks prior to sleep, but whether incorporating tasks into dreams influences memory consolidation is less clear. Some studies have shown an association between incorporating memory tasks into dreams and later memory performance, while others show either no effect or weaker effects. Potential reasons for this variation include the targeting of different stages of sleep – including rapid eye moment (REM) and non-REM stages (NREM) – small sample sizes, and the fact that many previous studies do not employ declarative memory tasks, which have been found to benefit more from sleep compared with tasks that target procedural memory.

 

In the current study. Schoch et al. (2023) ask whether dreams are an epiphenomenon of sleep-dependent memory processing or, instead, whether they play a key role in memory consolidation – and if so, whether that role differs for subjective experiences during NREM and REM sleep stages. Using a declarative memory task, a serial awakening paradigm (in which participants are woken and tested during NREM or REM stages), and targeted memory reactivation (TMR), the authors will test two main hypotheses: that incorporating picture categories of a declarative memory task leads to immediate (next morning) and sustained (4 days later) improvement in memory performance (especially for NREM dreams); and second, whether TMR influences the reported content of dreams. The authors also build in a range of control analyses to confirm that the task was incorporated successfully into dreams and that TMR benefited memory performance.

 

The Stage 1 manuscript was evaluated over two rounds of in-depth review, initially at Nature Communications before being transferred to PCI RR for further evaluation (see review history below for details). Based on detailed responses to the reviewers' comments, the recommender judged that the manuscript met the Stage 1 criteria and therefore awarded in-principle acceptance (IPA).
 
URL to the preregistered Stage 1 protocol: https://osf.io/7dwjz

 

Level of bias control achieved: Level 6. No part of the data or evidence that will be used to answer the research question yet exists and no part will be generated until after IPA.
 
List of eligible PCI RR-friendly journals:

 

 

1. Schoch, S. F., Ataei, S., Salvesen, L., Schredl, M., Windt, J., Bernadi, G., Rasch, B., Axmacher, N., & Desler, M. (2023). The relationship of memory consolidation with task incorporations into dreams – A registered report, in principle acceptance of Version 3 by Peer Community in Registered Reports. https://osf.io/7dwjz

The production effect is an intriguing memory phenomenon in which recall and recognition are improved when people read and study words aloud rather than silently. Although robust to a range of contexts, materials and manipulations, the underlying mechanisms that cause the production effect remain to be fully understood, largely due to the wide range of processes that are engaged during speaking compared to silent reading.

 

In the current study, Roembke and Brown (2024) ask whether semantic encoding – the encoding of new information based on its meaningful characteristics rather than sensory/perceptual characteristics – is a driving factor in production-enhanced memory. Across two carefully-controlled experiments in bilingual participants, the authors will test the hypothesis that the production effect should persist when items are matched in semantic but not other features at learning and recognition stages. If semantic encoding at least partially underpins the production effect, then they expect to observe it both when recognition items are presented as pictures or translations (their semantic recognition condition), and when recognition items match those at learning (their veridical recognition condition in which the same written words are presented at learning and recognition). Assuming also that the production effect does not rely exclusively on semantic encoding, the authors expect the production effect to be reduced in the semantic recognition conditions relative to veridical conditions in which words are matched on multiple linguistic features. 

 

The results of these experiments hold important implications for theoretical models of production-enhanced memory. If the authors find that the production effect persists when studied words can be recognised on their semantic features then this would suggest that production influences semantic encoding, which would in turn support theoretical models proposing that speaking engages modality-independent associations with semantic features. On the other hand, if no production effect is observed when participants are asked to recognise pictures or translations, this would raise the possibility that production may have little or no influence on semantic encoding, which would instead support alternative theories suggesting that speaking adds only modality-dependent features to memory traces.

 

The Stage 1 manuscript was evaluated over two rounds of in-depth review. Based on detailed responses to the reviewers' comments, the recommender judged that the manuscript met the Stage 1 criteria and therefore awarded in-principle acceptance (IPA).
 

URL to the preregistered Stage 1 protocol: https://osf.io/qc6rz
 
Level of bias control achieved: Level 6. No part of the data or evidence that will be used to answer the research question yet exists and no part will be generated until after IPA. 
 
List of eligible PCI RR-friendly journals:

 

 

Roembke, T. C. & Brown, R. M. (2024). The role of semantic encoding in production-enhanced memory: A registered report. In principle acceptance of Version 3 by Peer Community in Registered Reports. https://osf.io/qc6rz

How well animals may be able to cope with changes of habitat, specifically with rapid changes and thus novelty they encounter in an environment densely populated by humans, may be influenced by how they respond to novelty in general (Batisteli et al., 2022; Biondi et al., 2024; Castano et al., 2024; Heales et al., 2024). In considering this, it may be important to account for any difference in behavioural responses that animals exhibit when encountering a novel situation alone versus when they are doing so as part of a group.

 

Here, Allaert et al. (2025) tested how neophobia – the fear of unfamiliar objects – is affected by the social context in gulls, birds that are increasingly forced to live in urban environments due to the loss of natural coastlines. In this study, in which they reared herring gulls from egg and tested them taking into account that nestmates are not tested within the same groups, the authors found that the birds were faster to eat and spent more time in the zone of interest when they were tested in a group than when they were tested individually, specifically when a novel object was placed next to the food compared to when that object was a familiar one. The birds were also faster to enter the testing area when tested in a group, but this was not specific to the novel object condition. In addition to these changes in the average responses, the authors also report reduced variance when tested in a group in two of their three measures, namely in the latency to enter the testing area and time spent in the zone of interest.

 

The authors interpret their findings as being mostly in line with the ‘risk-dilution’ hypothesis, which is often considered in terms of predation risk (Krause & Buxton, 2002). They discuss possible reasons why other studies, with different species and different methodological setups, found support for alternative explanations.

 

The Stage 2 report was evaluated by the same two reviewers who had also reviewed the Stage 1 manuscript. In the revision, the authors focused on adding sex as a factor in their statistical models, which was the planned procedure for the statistical analyses in the Stage 1 report, and adding information regarding the problems encountered during testing and how these were handled. This specifically refers to the planned sample size (which the authors planned in the Stage 1 report taking into account both mortality and the fact that some birds would be not herring gulls but lesser black-backed gulls, which can only be established after hatching). However, there was higher than expected mortality, leading to a larger-than-planned overall reduction in sample size. During the study, the authors had contacted the recommender and discussed this issue, and the recommender advised on continuing the study and approved of the planned changes in the Stage 2 report. During the revision process, the authors added more information and also conducted an exploratory analysis, which included all birds, i.e. herring gulls and lesser black-backed gulls. This was suggested by a reviewer and the authors present this exploratory analysis in full in the supplemental material, while the main inferences are presented in the main text. In addition, during the Stage 2 review it became apparent that some minor details regarding the procedure would be useful to be included in the Stage 2 report, which the authors included in the Stage 2 revision. This did not alter the procedure as described in the Stage 1 report, but merely added more clarity to the text.

 

Based on detailed engagement with these points and the reviewers' comments, the recommender judged that the manuscript met the Stage 2 criteria and awarded a positive recommendation.

 

 
Level of bias control achieved: Level 6. No part of the data or evidence that was used to answer the research question was generated until after IPA.

 

 

• Peer Community Journal
• PeerJ
• Personality Science
• Royal Society Open Science

 

 

1. Allaert, R., Knoch, S., Braem, S., Debeer, D., Martel, A., Müller, W., Stienen, E., Lens, L., & Verbruggen, F. (2025). Neophobia across social contexts in juvenile Herring gulls [Stage 2]. Acceptance of Version 3 by Peer Community in Registered Reports. https://osf.io/b58ha

 

2. Batisteli, A. F., Pizo, M. A., & Sarmento, H. (2022). Female neophobia predicts the use of buildings as nesting sites in a Neotropical songbird. Animal Behaviour, 183, 151-157. https://doi.org/10.1016/j.anbehav.2021.11.008

 

3. Biondi, L. M., Medina, A., Bonetti, E. A., Paterlini, C. A., & Bó, M. S. (2024). Cognitive flexibility in a generalist raptor: a comparative analysis along an urbanization gradient. Behavioral Ecology, 35, arae025. https://doi.org/10.1093/beheco/arae025

 

4. Castano, M. V., Zumpano, F., Biondi, L. M., & García, G. O. (2024). Does urbanization affect behavioral responses to novel objects in marine birds? The Olrog’s Gull as a case of study. Urban Ecosystems, 27, 427-437. https://doi.org/10.1007/s11252-023-01465-2

 

5. Heales, H. E., Flood, N. J., Oud, M. D., Otter, K. A., & Reudink, M. W. (2024). Exploring differences in neophobia and anti-predator behaviour between urban and rural mountain chickadees. Journal of Urban Ecology, 10, juae01. https://doi.org/10.1093/jue/juae014

 

6. Krause, J. & Ruxton, G. (2002). Living in Groups. Oxford University Press, USA.

Vocal sounds, including both speech and non-speech sounds, have been found to activate the Superior Temporal Sulci and Gyri in comparison to non-vocal sounds. These regions, termed Temporal Voice Areas (TVAs), are considered to be involved in early voice processing and therefore critical for social interaction. TVA activation has been examined in Autism Spectrum Disorder (ASD) to determine if the characteristic difficulties in social communication and interaction are linked to an impaired early voice processing. Using functional magnetic resonance imaging (fMRI), one study found typical brain activation in TVAs for 15 out of 16 autistic participants (Schelinski et al., 2016), whereas another found atypical activation in 4 out of 5 autistic participants (Gervais et al., 2004).

 

Here, the inconsistencies in the previous literature propel Gautier et al. (2023) to examine brain activation of TVAs with a larger sample size (26 ASD and 26 non-ASD participants). Gautier et al. (2023) will present vocal sounds and non-vocal sounds to both groups of participants during fMRI and predict that fewer participants in the ASD group will show a preferential response to voices in TVAs compared to the non-ASD group. These results would suggest that symptoms of ASD interfere with early stages of social interaction, at the level of voice processing.

 

This Stage 1 manuscript was evaluated in an initial round by the co-recommenders and another two rounds of in-depth review by two expert reviewers. With these revisions, the recommenders judged that the manuscript met the Stage 1 criteria and awarded in-principle acceptance (IPA).

 

URL to the preregistered Stage 1 protocol: https://osf.io/538m4
 
Level of bias control achieved: Level 6. No part of the data or evidence that will be used to answer the research question yet exists and no part will be generated until after IPA.
 
List of eligible PCI RR-friendly journals:

 

 

References
 
1. Gautier, R., Houy-Durand, E., Barantin, L., Briend, F. & Latinus, M. (2023). Cortical voice processing in Autism Spectrum Disorder. In principle acceptance of Version 4 by Peer Community in Registered Reports. https://osf.io/538m4