In episodic recognition memory, differentiation is the assumption that a study item's pre-existing memory trace is updated when additional study for that item is provided. The differentiation models commonly suppose that episodic memory encoding conforms to this process. Although these models have received considerable support within the literature, results inconsistent with their predictions have also been found. The present paper examined conflicting findings that resulted from study list strength manipulations with rhyming word stimuli and semantically related stimuli. As part of the investigation into this discrepancy, 79 university students participated in a computer-based recognition memory task. In this task, word categories of varying length (short vs. long) and word type (rhyming vs. taxonomic) were presented either five times or once within a mixed study list. Following study, an old-new response paradigm was used to examine recognition memory performance. Results from both the rhyming and taxonomic category stimuli were largely consistent with the previous findings in the literature, indicating that word type does appear to influence recognition memory, even within a mixed study list. These findings are interpreted primarily in terms of word type similarity predictions made by one of the differentiation models. Other possible explanations are also discussed.

Past research has provided evidence for cultural differences in episodic memory when comparing European American and East Asian samples. However, cultural cognitive neuroscience has become over-dependent on European American vs. East Asian samples, which has left very little research into groups outside of this dichotomy. The aim of this dissertation was to address the need of more diverse samples in cultural cognitive neuroscience and to address the lack of research on Latinx biculturals. In this dissertation I explored how language could serve as a priming method to activate specific cultural systems, how bicultural Latinxs may switch cultural frames through language priming, and how priming of cultural systems affects their perception and recognition memory for certain visual information. The present study was designed to include a specific technique to investigate the potential cross-modal effect of cultural priming through language on visual cognition in bicultural and bilingual Latinxs. Results suggest that language did prime bicultural Latinxs to perform differently in a behavioral task, where images encoded in Spanish were more likely to be identified as incorrect and images encoded in English were more likely to be identified as correct. Additionally, we found that Cultural Blendedness directly predicted recognition accuracy, where higher identification led to more incorrect answers, and lower identification led to more correct answers. Implications, limitations, and areas of future study are discussed.

There is a prevalent assumption in the recognition memory literature that the terms “novelty” and “familiarity” are words ascribed to differing extremities of a single memory strength continuum. The aim of the current thesis was to integrate experimental methodologies across human and rodents to further investigate novelty processing at both a cognitive and neural level, and assess whether it is dissociable from familiarity processing. This dissociation was questioned at a cognitive level in human participants in Experiments 1 to 3 and at a neural level in rats in Experiment 4 and 5. Participants were found to differentially assess novelty and familiarity when making confidence judgements about the mnemonic status of an item (Experiment 1). Additionally, novelty and familiarity processing for questioned items were found to be dissimilarly affected by the presence of a concurrent item of varying mnemonic statuses (Experiment 2 and 3). The presence of a concurrent familiar item did not impact novelty processing in the perirhinal cortex (Experiment 4 and 5), yet disrupted the neural networks established to be differentially engaged by novelty and familiarity (Experiment 5). These findings challenge the assumption that the terms “novelty” and “familiarity” relate to a single recognition memory process. Finally, to allow integration of the findings from the human and rodent experiments, the relationship between measures or recognition memory obtained from spontaneous object recognition (SOR) task in rats and recognition memory measures estimated from signal-detection based models of recognition memory in humans was investigated (Experiment 6 and 7). This revealed that novelty preference in the SOR was positively correlated to measures of recognition memory sensitivity, but not bias. Thus, this thesis argues for the future inclusion of a novelty as a dissociable process from familiarity in our understanding of recognition memory, and for the integrations of experimental methodologies used to test recognition memory across species.

Novas informações assimiladas pelo sistema nervoso primeiramente ficam em um estado de labilidade para depois se estabilizarem através de um processo conhecido como consolidação, que envolve síntese de proteínas. Depois da reativação, uma memória previamente consolidada retorna ao seu estado de labilidade, e para que volte a ser estável, é necessário que haja novamente síntese de proteínas. Este segundo processo é chamado de reconsolidação. Recentemente os mecanismos moleculares e celulares envolvidos na regulação da síntese protéica relacionados à formação de memória de longa duração vêm sendo esclarecidos. A proteína alvo da rapamicina em mamíferos (mTOR) modula a plasticidade sináptica pela regulação da fosforilação de dois alvos: a proteína ribossomal S6K e a proteína de ligação 4E. A amígdala basolateral e o hipocampo dorsal são parte integrante do sistema neural envolvido na formação e expressão de diversos tipos de memórias. Estudos indicam que a via de sinalização da mTOR no hipocampo tem um papel importante na consolidação da memória de ratos submetidos a tarefa de esquiva inibitória e reconhecimento de objetos e na reconsolidação da memória de medo contextual condicionado. Contudo, estudos anteriores não avaliaram o efeito da inibição de mTOR amigdalar sobre a memória de esquiva inibitória e reconhecimento de objetos. O objetivo do presente trabalho é investigar o efeito da inibição de mTOR na amígdala basolateral por rapamicina na consolidação e reconsolidação da memória de esquiva inibitória e reconhecimento de objetos e comparar estes resultados com a inibição de mTOR no hipocampo. Ratos Wistar machos foram submetidos à cirurgia estereotáxica para implantação de cânulas na amígdala basolateral e hipocampo dorsal. Os animais foram submetidos à tarefa de esquiva inibitória, um modelo animal de memória de caráter aversivo, e a tarefa de reconhecimento de objetos, um modelo animal de memória de caráter pouco aversivo. Para investigar o efeito da inibição de mTOR na consolidação e reconsolidação da memória, os animais receberam microinfusões de rapamicina intra-amigdalar e intra-hipocampal em diferentes tempos em torno do treino e do teste. Nós demonstramos que a via de sinalização de mTOR na amígdala basolateral é necessária para consolidação da memória de esquiva inibitória e de reconhecimento de objetos. Nós também mostramos que a reativação torna a memória novamente suscetível e sensível à inibição de mTOR por rapamicina. / Memory formation requires protein synthesis, but only recently the cellular and molecular mechanisms involved in the regulation of protein synthesis related to the formation of long term memory has been elucidated. During memory formation, new information is acquired by the central nervous system as an initially fragile trace that over time becomes stable through a process known as consolidation. After reactivation, previously consolidated memories might return to a labile state, requiring a new round of protein synthesis to be restabilized. This second process is called reconsolidation. The basolateral amygdala and dorsal hippocampus are part of the neural systems involved in the formation and expression of several types of memory. One key regulator of protein synthesis is mTOR, a protein critical for different forms of synaptic plasticity by regulation of two targets: S6K and 4EBP. Evidence indicates that the mTOR signaling pathway in hippocampus has an important role in consolidation in rats of inhibitory avoidance and object recognition in rats, as well as in reconsolidation of contextual fear conditioning. However, previous studies have not examinated the effect of amygdalar mTOR inhibition on reconsolidation of inhibitory avoidance and object recognition. The aim of the present study was to evaluate the effect of amygdalar mTOR inhibition by rapamycin on consolidation and reconsolidation of inhibitory avoidance and object recognition, and compare the results with those obtained with hippocampal mTOR inhibition. Male rats Wistar underwent stereotaxic surgeries for cannulae implantation above the basolateral amygdala or dorsal hippocampus. After recovery, the animals were trained in inhibitory avoidance, an aversive memory task, or object recognition, a less aversive task. To investigate the effect of mTOR inhibition on memory consolidation and reconsolidation, we administered rapamycin, a specific mTOR inhibitor, into the basolateral amygdala or the dorsal hippocampus before or after training or reactivation. Our results provide evidence that mTOR in the basolateral amygdala and hippocampus might play a role in inhibitory avoidance and object recognition memory formation and reconsolidation.

Made available in DSpace on 2014-12-17T15:37:19Z (GMT). No. of bitstreams: 1 YalkiriaGVDB.pdf: 279553 bytes, checksum: 548ebdc7f23186b939bb4472661135c5 (MD5) Previous issue date: 2006-08-18 / Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico / As we grow old, there are many cognitive processes which decline in the human brain. One of them is the memory, a function that allows retention and posterior use of knowledge learned during the life, understood as a result of multiple systems highly organized and spread in several neural regions. This work aimed to evaluate the recognition memory in adults over 45 years old through words and pictures recognition tasks and the use of two codification or learning conditions (same distracters and different distracters). Twelve individuals were studied (6 men and 6 women) aged between 45 and 88 years old and with similar demographic characteristics. They presented better performance on picture tasks rather than word tasks. Better results were also verified when the codification context had different distracters, which significantly reflected in a long term principally in elderly individuals. The results reached suggest that the codification context influenced the lists of pictures and words learning, mainly for the elderly ones, when compared to adults, and that these results can be related to the phenomena involved with the recognition memory, the recollection and familiarity / Com o decorrer da idade, s?o v?rios os processos cognitivos que declinam no c?rebro humano. Um deles ? a mem?ria, fun??o que permite a reten??o e posterior utiliza??o dos conhecimentos apreendidos ao longo da vida, entendendo-a como o resultado de m?ltiplos sistemas altamente organizados e espalhados em diversas regi?es neurais. O presente trabalho teve como objetivo avaliar a mem?ria de reconhecimento em indiv?duos adultos com mais de 45 anos, atrav?s de tarefas de reconhecimento de palavras e de figuras e o uso de duas condi??es de codifica??o ou aprendizagem (com distratores iguais e com distratores diferentes). Foram estudados 12 sujeitos (6 homens e 6 mulheres) com idade entre 45 a 88 anos e caracter?sticas demogr?ficas semelhantes. Os sujeitos apresentaram melhor desempenho nas tarefas de figuras do que nas de palavras. Melhores resultados tamb?m foram verificados quando o contexto de codifica??o se deu com distratores diferentes, o que se refletiu significativamente a longo prazo principalmente em indiv?duos idosos. Os resultados alcan?ados sugerem que o contexto de codifica??o influenciou a aprendizagem de listas de figuras e de palavras, principalmente para os indiv?duos idosos, quando comparados com adultos maduros, e que estes resultados podem estar relacionados aos fen?menos envolvidos com a mem?ria de reconhecimento, a recorda??o e a familiaridade

Novas informações assimiladas pelo sistema nervoso primeiramente ficam em um estado de labilidade para depois se estabilizarem através de um processo conhecido como consolidação, que envolve síntese de proteínas. Depois da reativação, uma memória previamente consolidada retorna ao seu estado de labilidade, e para que volte a ser estável, é necessário que haja novamente síntese de proteínas. Este segundo processo é chamado de reconsolidação. Recentemente os mecanismos moleculares e celulares envolvidos na regulação da síntese protéica relacionados à formação de memória de longa duração vêm sendo esclarecidos. A proteína alvo da rapamicina em mamíferos (mTOR) modula a plasticidade sináptica pela regulação da fosforilação de dois alvos: a proteína ribossomal S6K e a proteína de ligação 4E. A amígdala basolateral e o hipocampo dorsal são parte integrante do sistema neural envolvido na formação e expressão de diversos tipos de memórias. Estudos indicam que a via de sinalização da mTOR no hipocampo tem um papel importante na consolidação da memória de ratos submetidos a tarefa de esquiva inibitória e reconhecimento de objetos e na reconsolidação da memória de medo contextual condicionado. Contudo, estudos anteriores não avaliaram o efeito da inibição de mTOR amigdalar sobre a memória de esquiva inibitória e reconhecimento de objetos. O objetivo do presente trabalho é investigar o efeito da inibição de mTOR na amígdala basolateral por rapamicina na consolidação e reconsolidação da memória de esquiva inibitória e reconhecimento de objetos e comparar estes resultados com a inibição de mTOR no hipocampo. Ratos Wistar machos foram submetidos à cirurgia estereotáxica para implantação de cânulas na amígdala basolateral e hipocampo dorsal. Os animais foram submetidos à tarefa de esquiva inibitória, um modelo animal de memória de caráter aversivo, e a tarefa de reconhecimento de objetos, um modelo animal de memória de caráter pouco aversivo. Para investigar o efeito da inibição de mTOR na consolidação e reconsolidação da memória, os animais receberam microinfusões de rapamicina intra-amigdalar e intra-hipocampal em diferentes tempos em torno do treino e do teste. Nós demonstramos que a via de sinalização de mTOR na amígdala basolateral é necessária para consolidação da memória de esquiva inibitória e de reconhecimento de objetos. Nós também mostramos que a reativação torna a memória novamente suscetível e sensível à inibição de mTOR por rapamicina. / Memory formation requires protein synthesis, but only recently the cellular and molecular mechanisms involved in the regulation of protein synthesis related to the formation of long term memory has been elucidated. During memory formation, new information is acquired by the central nervous system as an initially fragile trace that over time becomes stable through a process known as consolidation. After reactivation, previously consolidated memories might return to a labile state, requiring a new round of protein synthesis to be restabilized. This second process is called reconsolidation. The basolateral amygdala and dorsal hippocampus are part of the neural systems involved in the formation and expression of several types of memory. One key regulator of protein synthesis is mTOR, a protein critical for different forms of synaptic plasticity by regulation of two targets: S6K and 4EBP. Evidence indicates that the mTOR signaling pathway in hippocampus has an important role in consolidation in rats of inhibitory avoidance and object recognition in rats, as well as in reconsolidation of contextual fear conditioning. However, previous studies have not examinated the effect of amygdalar mTOR inhibition on reconsolidation of inhibitory avoidance and object recognition. The aim of the present study was to evaluate the effect of amygdalar mTOR inhibition by rapamycin on consolidation and reconsolidation of inhibitory avoidance and object recognition, and compare the results with those obtained with hippocampal mTOR inhibition. Male rats Wistar underwent stereotaxic surgeries for cannulae implantation above the basolateral amygdala or dorsal hippocampus. After recovery, the animals were trained in inhibitory avoidance, an aversive memory task, or object recognition, a less aversive task. To investigate the effect of mTOR inhibition on memory consolidation and reconsolidation, we administered rapamycin, a specific mTOR inhibitor, into the basolateral amygdala or the dorsal hippocampus before or after training or reactivation. Our results provide evidence that mTOR in the basolateral amygdala and hippocampus might play a role in inhibitory avoidance and object recognition memory formation and reconsolidation.

Novas informações assimiladas pelo sistema nervoso primeiramente ficam em um estado de labilidade para depois se estabilizarem através de um processo conhecido como consolidação, que envolve síntese de proteínas. Depois da reativação, uma memória previamente consolidada retorna ao seu estado de labilidade, e para que volte a ser estável, é necessário que haja novamente síntese de proteínas. Este segundo processo é chamado de reconsolidação. Recentemente os mecanismos moleculares e celulares envolvidos na regulação da síntese protéica relacionados à formação de memória de longa duração vêm sendo esclarecidos. A proteína alvo da rapamicina em mamíferos (mTOR) modula a plasticidade sináptica pela regulação da fosforilação de dois alvos: a proteína ribossomal S6K e a proteína de ligação 4E. A amígdala basolateral e o hipocampo dorsal são parte integrante do sistema neural envolvido na formação e expressão de diversos tipos de memórias. Estudos indicam que a via de sinalização da mTOR no hipocampo tem um papel importante na consolidação da memória de ratos submetidos a tarefa de esquiva inibitória e reconhecimento de objetos e na reconsolidação da memória de medo contextual condicionado. Contudo, estudos anteriores não avaliaram o efeito da inibição de mTOR amigdalar sobre a memória de esquiva inibitória e reconhecimento de objetos. O objetivo do presente trabalho é investigar o efeito da inibição de mTOR na amígdala basolateral por rapamicina na consolidação e reconsolidação da memória de esquiva inibitória e reconhecimento de objetos e comparar estes resultados com a inibição de mTOR no hipocampo. Ratos Wistar machos foram submetidos à cirurgia estereotáxica para implantação de cânulas na amígdala basolateral e hipocampo dorsal. Os animais foram submetidos à tarefa de esquiva inibitória, um modelo animal de memória de caráter aversivo, e a tarefa de reconhecimento de objetos, um modelo animal de memória de caráter pouco aversivo. Para investigar o efeito da inibição de mTOR na consolidação e reconsolidação da memória, os animais receberam microinfusões de rapamicina intra-amigdalar e intra-hipocampal em diferentes tempos em torno do treino e do teste. Nós demonstramos que a via de sinalização de mTOR na amígdala basolateral é necessária para consolidação da memória de esquiva inibitória e de reconhecimento de objetos. Nós também mostramos que a reativação torna a memória novamente suscetível e sensível à inibição de mTOR por rapamicina. / Memory formation requires protein synthesis, but only recently the cellular and molecular mechanisms involved in the regulation of protein synthesis related to the formation of long term memory has been elucidated. During memory formation, new information is acquired by the central nervous system as an initially fragile trace that over time becomes stable through a process known as consolidation. After reactivation, previously consolidated memories might return to a labile state, requiring a new round of protein synthesis to be restabilized. This second process is called reconsolidation. The basolateral amygdala and dorsal hippocampus are part of the neural systems involved in the formation and expression of several types of memory. One key regulator of protein synthesis is mTOR, a protein critical for different forms of synaptic plasticity by regulation of two targets: S6K and 4EBP. Evidence indicates that the mTOR signaling pathway in hippocampus has an important role in consolidation in rats of inhibitory avoidance and object recognition in rats, as well as in reconsolidation of contextual fear conditioning. However, previous studies have not examinated the effect of amygdalar mTOR inhibition on reconsolidation of inhibitory avoidance and object recognition. The aim of the present study was to evaluate the effect of amygdalar mTOR inhibition by rapamycin on consolidation and reconsolidation of inhibitory avoidance and object recognition, and compare the results with those obtained with hippocampal mTOR inhibition. Male rats Wistar underwent stereotaxic surgeries for cannulae implantation above the basolateral amygdala or dorsal hippocampus. After recovery, the animals were trained in inhibitory avoidance, an aversive memory task, or object recognition, a less aversive task. To investigate the effect of mTOR inhibition on memory consolidation and reconsolidation, we administered rapamycin, a specific mTOR inhibitor, into the basolateral amygdala or the dorsal hippocampus before or after training or reactivation. Our results provide evidence that mTOR in the basolateral amygdala and hippocampus might play a role in inhibitory avoidance and object recognition memory formation and reconsolidation.

Introdução: O etilismo é uma doença crônica e progressiva que tem um impacto significante nos valores sociais e econômicos da sociedade. A interrupção abrupta do consumo crônico de etanol pode levar à Síndrome de Abstinência alcoólica (SAA) com repercussões na saúde do indivíduo. Atualmente, muita atenção também tem sido dada ao consumo espaçado de etanol em doses elevadas, caracterizado como binge. Dentre as várias consequências do consumo agudo e/ou crônico do etanol, podem-se destacar os déficits em teste de aprendizagem e de memória. Objetivos: verificar se a abstinência ao etanol após o consumo involuntário ou semivoluntário de etanol (crônico ou agudo) é capaz de interferir na aprendizagem, na memória e na ansiedade de ratos adultos. Materiais e Métodos: Foram utilizados 196 ratos albinos, Wistar e machos, com 21 dias de vida. Inicialmente os animais foram divididos em dois grandes grupos para compor o Estudo 1 ou o estudo 2. No estudo 1 a via de administração foi semivoluntária (etanol a 6%) e no estudo 2 foi involuntária (por gavagem intragástrica- 1g etanol/kg). Em ambos os estudos os animais foram divididos novamente em relação ao tipo de bebida que receberiam (água ou etanol) e tempo de consumo (agudo- 2 horas ou crônico- 21 dias, sendo que no estudo 2 a ingestão etílica aconteceu a cada 3 dias). No 23º dia (após 48 horas da última ingestão etílica) os animais foram testados no Teste de Memória de Reconhecimento (TMR), no Labirinto em Cruz Elevado (LCE) e no Labirinto Aquático de Morris (LAM) por dois dias consecutivos e retestados após 28 dias. Resultados: No estudo 1 os resultados indicaram que a abstinência ao etanol após o consumo agudo ou crônico de etanol não foi capaz de alterar a aprendizagem e a memória espacial no LAM, porém prejuízos na memória espacial de longo prazo foram observados nos animais submetidos ao consumo agudo de etanol. Não foram observadas alterações na Memória de Reconhecimento na Sessão treino e na Memória de Reconhecimento de Curto Prazo, porém a exposição aguda ao etanol foi capaz de gerar prejuízos na memória de Reconhecimento de Longo Prazo. Não houve diferenças nos níveis de ansiedade dos animais do estudo. Em relação ao estudo 2, foi possível observar que a abstinência do etanol após o consumo agudo foi capaz de gerar um prejuízo na memória espacial de curto prazo e que o consumo crônico e agudo de etanol não foram capaz de prejudicar a Memória de Reconhecimento dos animais estudados. Ainda que, os animais expostos ao consumo agudo e crônico de etanol, em abstinência ao etanol de 48 horas apresentaram níveis de ansiedade elevados. Conclusão: O etanol influencia de forma diferente a memória espacial, a memória de reconhecimento e os níveis de ansiedade a depender da via de administração (e, portanto da quantidade de etanol ingerida) e do tempo de consumo. / Introduction: Alcoholism is a chronic and progressive disease that has a significant impact on social and economic values of society. Abrupt withdrawal of chronic ethanol consumption can lead to alcohol withdrawal syndrome (AWS) which impacts on the health of the individual. Currently, much attention has also been attributed to the spaced ethanol consumption in high doses, characterized as \"binge\". Among the many consequences of acute and/or chronic consumption ethanol, can highlight the deficits in learning and memory test. Objectives: verify if abstinence to ethanol after the involuntary consumption of ethanol or semi-voluntary (chronic or acute) can interfere in the learning, memory and anxiety in adult rats Materials and Methods: were used 196 albino rats Wistar and males, with 21 days of life. Initially, the animals were divided into two groups to compose the study 1 or 2. In study 1 the administration route was semi voluntary (6% ethanol) and in Study 2 was involuntary (by gavage intragástrica- ethanol 1g / kg). In both studies, the animals were divided again in relation to the type of beverage that receive (water or ethanol) and time consumption (acute- 2 hours or chronic for 21 days, whereas in Study 2 the alcohol consumption occurred every 3 days). On the 23rd days (48 hours after the last alcohol consumption) the animals were tested in Recognition Memory Test (RMT), the Elevated Plus Maze (EPM) and Morris Water Maze (MAM) for two consecutive days (and retested after 28 days). Results: In study 1 the results indicated that abstinence to ethanol after acute or chronic ethanol consumption was not able to alter the learning and spatial memory in LAM, but damage on long-term spatial memory were observed in animals submitted to consumption acute ethanol. No changes were observed in recognition memory in Session training and Short-term recognition memory, but the acute ethanol exposure was able to generate damages on long-term recognition memory. There were no differences in anxiety levels of study animals. Regarding the study 2, we observed that abstinence after acute ethanol consumption was able to generate damage in spatial memory short term and that chronic and acute consumption of ethanol were not able to alter the Recognition Memory of animals studied. Although, animals exposed to acute and chronic ethanol consumption in abstinence to 48 hours ethanol showed elevated levels of anxiety. Conclusion: Ethanol affects differently the spatial memory, recognition memory and anxiety levels depending on the route of administration (and therefore the amount of intake of ethanol) and of the time consumption.

Signal Detection Theory (SDT; Green & Swets, 1966) is a well-established technique to analyze accuracy data in a number of experimental paradigms in psychology, most notably memory and perception, by separating a response bias/criterion from the theoretically bias-free discriminability/sensitivity. As SDT has traditionally been applied, the researcher may be confronted with loss in statistical power and erroneous inferences. A generalized linear mixed-effects modeling (GLMM) approach is presented and advantages with regard to power and precision are demonstrated with an example analysis. Using this approach, a correlation of response bias and sensitivity was detected in the dataset, especially prevalent at the item level, though a correlation between these measures is usually not found to be reported in the memory literature. Directions for future extensions of the method as well as a brief discussion of the correlation between response bias and sensitivity are enclosed. / Graduate / 2019-03-22

There is an extensive debate in the adult literature on whether recognition memory can better be explained by a single- or a dual-process account. Single-process accounts assume that a single memory strength signal underlies recognition. Dual-process accounts propose two independent processes, namely recollection (slow and associated with contextual details) and familiarity (fast and automatic). The aim of this dissertation was to advance this debate using a cognitive developmental approach. By investigating age-related changes of recognition memory across childhood as a function of theoretically motivated experimental manipulations, predictions drawn from single- and dual-process models of recognition memory were tested. We adapted the Process Dissociation Paradigm (PDP; Jacoby, 1991) to disentangle processes underlying recognition memory in 5-, 7-, and 11-year-olds and adults using a Dual-Process Signal Detection cognitive modelling approach (DPSD; Yonelinas, 1996). Experiments 1 – 6 demonstrated that 5-year-olds are able to recollect items based on perceptual details. Consistent with dual-process theory, across all age groups a response time limit decreased recollection while leaving familiarity unaffected (Chapter 2). Converging evidence consistent with dissociations during childhood was found after repeated item presentation (Chapter 3). Finally, after a thorough empirical validation of our approach, the new paradigm was used to investigate the developmental perceptual to semantic shift (Chapter 4). These findings, using a double dissociation logic, have advanced the theoretical debate on the nature of recognition memory by showing that one process is insufficient to account for the developmental and experimental findings reported here. Recollection and familiarity follow different developmental trajectories and are affected by encoding and retrieval manipulations (i.e., repetition and time limits). This provides a challenge for existing theories of recognition memory.