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PubMed1993

Episodic encoding of voice attributes and recognition memory for spoken words.

Recognition memory for spoken words was investigated with a continuous recognition memory task. Independent variables were number of intervening words (lag) between initial and subsequent presentations of a word, total number of talkers in the stimulus set, and whether words were repeated in the same voice or a different voice. In Experiment 1, recognition judgements were based on word identity alone. Same-voice repetitions were recognized more quickly and accurately than different-voice repetitions at all values of lag and at all levels of talker variability. In Experiment 2, recognition judgments were based on both word identity and voice identity. Subjects recognized repeated voices quite accurately. Gender of the talker affected voice recognition but not item recognition. These results suggest that detailed information about a talker's voice is retained in long-term episodic memory representations of spoken words.

Adult↗

PubMed1978

Facilitation of infants' recognition memory.

Infant's recognition memory, defined by novelty preferences, was found to be improved by providing 5--7-month-old infants with discriminable but related targets during the familiarization period. Facilitation of recognition was found for both photos of faces and for abstract patterns. It was necessary to present only 1 associated stimulus along with the to-be-remembered target in order to aid recognition. Such facilitation was dependent upon the kind of related target shown for study and was more likely to be demonstrated when simultaneous rather than successive exposure to related instances was allowed.

Child Development↗

PubMed2004

Encoding context and false recognition memories.

False recognition of an extralist word that is thematically related to all words of a study list may reflect internal activation of the theme word during encoding followed by impaired source monitoring at retrieval, that is, difficulty in determining whether the word had actually been experienced or merely thought of. To assist source monitoring, distinctive visual or verbal contexts were added to study words at input. Both types of context produced similar effects: False alarms to theme-word (critical) lures were reduced; remember judgements of critical lures called old were lower; and if contextual information had been added to lists, subjects indicated as much for list items and associated critical foils identified as old. The visual and verbal contexts used in the present studies were held to disrupt semantic categorisation of list words at input and to facilitate source monitoring at output.

Analysis of Variance↗

PubMed1996

The sensory match effect in recognition memory: perceptual fluency or episodic trace?

The sensory match effect in recognition memory refers to the finding that recognition is better when the sensory form in which an item is tested is the same as that in which it was studied. This paper examines the basis for the sensory match effect by manipulating whether a studied fragmented picture is tested with the same or a complementary set of fragments in a recognition memory test (Experiment 1) and in a fragment-identification test (Experiment 2). Assuming that fragment identification is a direct measure of perceptual fluency, we expected identical patterns of results across the two tests if perceptual fluency accounted for the sensory match effect in recognition memory. Instead, recognition memory showed a robust overall sensory match effect (the same fragmented image was recognized better than the complementary image), whereas fragment identification showed no overall sensory match effect (the same fragmented image was identified no better than the complementary fragmented image). Experiments 3 and 4 combined the two responses and showed that the basis for the sensory match effect in recognition memory was a subject's ability to recognize the matching fragments in the absence of conceptual information (when the test stimulus could not be identified), supporting the idea that the episodic trace of the sensory code is responsible for the sensory match effect in recognition memory. Experiment 5 demonstrated that subjects are able to use this sensory code as the sole basis for recognition memory.

Form Perception↗

PubMed2003

Effects of intra-accumbens focal administrations of glutamate antagonists on object recognition memory in mice.

Generally recognition memory is distinguished into spatial and object memories that have been suggested to relay at a cortical level on different neural substrates. Recent studies point to a possible involvement of the nucleus accumbens (Nac) in spatial memory, demonstrating that blockade of glutamate antagonists within this structure impairs acquisition and consolidation of spatial information, while not many data are available on the potential role of this structure in object recognition. Thus in this study we wanted to investigate the effects of intra-accumbens focal administrations of NMDA antagonist, AP-5 (0.05, 0.1, 0.15 or 0.2 microg per side), and AMPA antagonist, DNQX (0.0005 or 0.001 microg per side), in object recognition memory. The spontaneous preference displayed by mice for novel objects was taken as an index for measuring object recognition. Pre-training focal administrations of both antagonists impaired the ability of mice to selectively explore the novel object in test session. However, the AMPA antagonist induced also a decrease in exploration and locomotion. In order to assess whether glutamate receptors located within the Nac were also involved in subsequent steps of object information processing, we performed additional experiments injecting AP-5 and DNQX immediately after training and testing the animals 24-h later. In this case, AP-5 but not the AMPA antagonist impaired exploration of the novel object. These results demonstrate that the Nac is involved in object recognition, and confirm that the different glutamate receptors mediate different component of information processing within the accumbens.

2-Amino-5-phosphonovalerate↗

PubMed1977

Marijuana and memory impairment: effect on free recall and recognition memory.

The effect of marijuana on memory was evaluated by presenting two groups of 17 male volunteers with lists of repeated or nonrepeated words following administration of a single marijuana cigarette containing 14 mg delta9-THC. An immediate free recall, final free recall and recognition memory test followed. Results indicated that marijuana significantly decreased immediate and final free recall but only slightly influenced recognition memory. Rate of acquisition on the repeated lists was the same for both groups. Long term retention of encoded information was not influenced by marijuana. The shape of the serial position curves departed slightly from those reported by other investigators in that some effects of the drug on the recency portion of the curve were noted. Both internal and external intrusions were elevated under marijuana.

Adult↗

PubMed1980

Evoked potential correlates of recognition memory.

During word recognition tasks, differences in the stimulus related potentials to 'old' (previously presented) and 'new' (not previously presented) words occurred as early as 160-190 ms after stimulus onset (N1) as well as in the late component of the wave forms (P3). The N1 differences may possibly reflect underlying neural activity directly related to the recognition memory process.

Electroencephalography↗

PubMed1998

Internal consistency of the Warrington Recognition Memory Test.

The Recognition Memory Test is frequently used to assess memory; however, one of the commonly cited limitations is a lack of data on reliability. The current study was undertaken to estimate the internal consistency reliability of the test with a sample of 72 persons with traumatic brain injury. Acceptable estimates of internal consistency for both subtests were obtained.

Adolescent↗

PubMed1996

Olfactory recognition memory.

Olfactory recognition which occurs in the context pregnancy block by male pheromones is acquired with one-trial learning contingent on mating. A memory trace is established in the accessory bulb (AOB) and is represented by a gain in Gaba-ergic feedback inhibition of granule cells on excitatory glutaminergic mitral cells. This occurs in the sub-population of mitral cells that specifically respond to an individual male's pheromones, and is dependent on noradrenaline release at mating. Although relatively simple, the AOB has both structural and functional similarities with other trilaminar neural structures involved in learning, which suggests some evolutionary conservation of mechanisms subserving memory.

Animals↗

PubMed2000

ROC curves and confidence judgements in recognition memory.

Most models of recognition memory rely on a strength/familiarity-based signal detection account that assumes that the processes giving rise to a confidence judgment are the same as those giving rise to an old-new decision. Confidence is assumed to be scaled directly from the perceived familiarity of a probe. This assumption was tested in 2 experiments that examine the shape of confidence-based z receiver operating characteristic (zROC) curves under different levels of response bias induced by changing stimulus probabilities (Experiment 1) and payoffs (Experiment 2). Changes in the shape of the zROC curves with bias indicate that confidence is not scaled directly from perceived familiarity or likelihood. A model of information accumulation in recognition memory is proposed that can account for the observed effects.

Adult↗

PubMed1992

Cuing effects and associative information in recognition memory.

Item recognition requires discrimination of studied words from nonstudied words. Associative recognition requires subjects to discriminate studied word groups from recombinations of words from different groups. Cued recognition requires the same old-new discrimination as item recognition, but list items are presented as cues along with the test item. The results from three experiments show (1) little or no effect of cuing for low-frequency words, but (2) positive cuing effects for high-frequency words; (3) increasing levels of overall performance with increases in study time, but (4) unchanging effects of cuing with study time; and (5) stronger positive cuing effects for two cues than for one cue. Five models (Independent Cue Model, Matrix model, MINERVA 2, SAM, and TODAM) were fit to the data of Experiment 1. Each model has trouble with at least one aspect of the results. Theoretical implications and modifications are discussed at length.

Adult↗

PubMed2006

Why does brain damage impair memory? A connectionist model of object recognition memory in perirhinal cortex.

Object recognition is the canonical test of declarative memory, the type of memory putatively impaired after damage to the temporal lobes. Studies of object recognition memory have helped elucidate the anatomical structures involved in declarative memory, indicating a critical role for perirhinal cortex. We offer a mechanistic account of the effects of perirhinal cortex damage on object recognition memory, based on the assumption that perirhinal cortex stores representations of the conjunctions of visual features possessed by complex objects. Such representations are proposed to play an important role in memory when it is difficult to solve a task using representations of only individual visual features of stimuli, thought to be stored in regions of the ventral visual stream caudal to perirhinal cortex. The account is instantiated in a connectionist model, in which development of object representations with visual experience provides a mechanism for judgment of previous occurrence. We present simulations addressing the following empirical findings: (1) that impairments after damage to perirhinal cortex (modeled by removing the "perirhinal cortex" layer of the network) are exacerbated by lengthening the delay between presentation of to-be-remembered items and test, (2) that such impairments are also exacerbated by lengthening the list of to-be-remembered items, and (3) that impairments are revealed only when stimuli are trial unique rather than repeatedly presented. This study shows that it may be possible to account for object recognition impairments after damage to perirhinal cortex within a hierarchical, representational framework, in which complex conjunctive representations in perirhinal cortex play a critical role.

Brain Injuries↗

PubMed2004

On the delay-dependent involvement of the hippocampus in object recognition memory.

The role of the hippocampus in object recognition memory processes is unclear in the current literature. Conflicting results have been found in lesion studies of both primates and rodents. Procedural differences between studies, such as retention interval, may explain these discrepancies. In the present study, acute lidocaine administration was used to temporarily inactivate the hippocampus prior to training in the spontaneous object recognition task. Male C57BL/6J mice were administered bilateral lidocaine (4%, 0.5 microl/side) or aCSF (0.5 microl/side) directly into the CA1 region of the dorsal hippocampus 5 min prior to sample object training, and object recognition memory was tested after a short ( 5 min) or long (24 h) retention interval. There was no effect of intra-hippocampal lidocaine on the time needed for mice to accumulate sample object exploration, suggesting that inactivation of the hippocampus did not affect sample session activity or the motivation to explore objects. Lidocaine-treated mice exhibited impaired object recognition memory, measured as reduced novel object preference, after a 24 h but not a 5 min retention interval. These data support a delay-dependent role for the hippocampus in object recognition memory, an effect consistent with the results of hippocampal lesion studies conducted in rats. However, these data are also consistent with the view that the hippocampus is involved in object recognition memory regardless of retention interval, and that object recognition processes of parahippocampal structures (e.g., perirhinal cortex) are sufficient to support object recognition memory over short retention intervals.

Anesthetics, Local↗

PubMed1998

Recognition memory in rats--III. Neurochemical substrates.

In the first part of three overviews on recognition memory in the rat, we discussed the tasks employed to study recognition memory. In the second part, we discussed the neuroanatomical systems thought to be of importance for the mediation of recognition memory in the rat. In particular, we delineated two parallel-distributed neuronal networks, one that is essential for the processing of non-spatial/item recognition memory processes and incorporates the cortical association areas such as TE1, TE2 and TE3, the rhinal cortices, the mediodorsal thalamic nucleus and prefrontal cortical areas (Network 1), the other comprising of the hippocampus, mamillary bodies, anterior thalamic nuclei and medial prefrontal areas (Network 2), suggested to be pivotal for the processing of spatial recognition memory. The next step will progress to the level of the neurotransmitters thought to be involved. Current data suggest that the majority of drugs have non-specific, i.e. delay-independent effects in tasks measuring recognition memory. This may be due to attentional, motivational or motoric changes. Alternatively, delay-independent effects may result from altered acquisition/encoding rather than from altered retention. Furthermore, the neurotransmitter systems affected by these drugs could be important as modulators rather than as mediators of recognition memory per se. It could, of course, also be the case that systemic treatment induces non-specific effects which overshadow any specific, delay-dependent, effect. This possibility receives support from lesion experiments (for example, of the septohippocampal cholinergic system) or studies employing local intracerebral infusion techniques. However, it is evident that those delay-dependent effects are relatively subtle and more readily seen in delayed response paradigms, which tax spatial recognition memory. One interpretation of these results could be that some neurotransmitter systems are more involved in spatial than in item recognition memory processes. However, performance in delayed response tasks can be aided by mediating strategies. Drugs or lesions can alter those strategies, which could equally explain some of the (delay-dependent) drug effects on delayed responding. Thus, it is evident that neither of the neurotransmitter systems reviewed (glutamate, GABA, acetylcholine, serotonin, dopamine and noradrenaline) can be viewed as being directly and exclusively concerned with storage/retention. Rather, our model of recognition memory suggests that information about previously encountered items is differentially processed by distinct neural networks and is not mediated by a single neurotransmitter type.

Animals↗

PubMed2004

Impaired odor recognition memory in patients with hippocampal lesions.

In humans, impaired recognition memory following lesions thought to be limited to the hippocampal region has been demonstrated for a wide variety of tasks. However, the importance of the human hippocampus for olfactory recognition memory has scarcely been explored. We evaluated the ability of memory-impaired patients with damage thought to be limited to the hippocampal region to recognize a list of odors. The patients were significantly impaired after a retention delay of 1 h. Olfactory sensitivity was intact. This finding is in agreement with earlier reports that rats with hippocampal lesions exhibited memory impairment on an odor delayed nonmatching to sample task (after 30 min and 1 h) and that patients with damage thought to be limited to the hippocampal region were impaired on an odor span memory task. Olfactory recognition memory, similar to recognition memory in other sensory modalities, depends on the integrity of the hippocampal region.

Adult↗

PubMed1995

The word frequency effect in recognition memory versus repetition priming.

The role of word frequency in recognition memory and repetition priming was investigated by using a manipulation of attention. In Experiment 1, the lexical decision task produced greater repetition priming for low-frequency words than for high-frequency words following either the attended or the unattended study condition. The recognition memory test, on the other hand, showed a low-frequency word advantage only following the attended study condition. Furthermore, this advantage was limited to the measure of recognition memory based on conscious recollection of the study episode. In Experiment 2, a speeded recognition memory test replicated the pattern obtained with the unspeeded recognition memory test in Experiment 1. These results argue against the view that the word frequency effects in recognition memory and repetition priming have the same origin. Instead, the results suggest that the word frequency effect in recognition memory has its locus in conscious recollection.

Attention↗

PubMed1978

Influence of active encoding on tactile recognition memory for common objects.

Active tactile recognition memory for common objects is compared with passive touch. The recognition memory test occure after a delay between inspection and test of seven days. Three groups of five each have the following conditions and results: Group I manipulated objects at both inspection and test to obtain a recognition rate of 87.9%; Group II manipulated objects at inspection but not at test, i.e., passive touch, to produce a recognition rate of 80.7%; Group III manipulated objects at test but not at inspection to perform at a 72.5% accuracy rate. Object manipulation had a significant effect and the group means were all significantly different (p less than or equal to .05), with the largest performance decrement due to passive touch at encoding. Generally, the findings implicated the importance of object identity in tactile recognition memory which, in turn, is supportive of the depth-of-processing approach to memory.

Discrimination, Psychological↗

PubMed1998

Recognition memory: neuronal substrates of the judgement of prior occurrence.

Recognition memory relies on two processes: (i) identification and (ii) judgement concerning prior occurrence. A system centred on perirhinal cortex appears to be responsible for judgement of prior occurrence based on discrimination of the familiarity of stimuli or their recency of occurrence; in contrast, a hippocampal system probably supplies information concerning the episodic, contextual aspects of recognition memory. This review chiefly concerns the perirhinal system and, in particular, neurones that signal the prior occurrence of stimuli by a decrease in response. Details concerning such decremental responses are given and it is argued that such responses in perirhinal cortex are adequate for and central to discrimination of stimulus familiarity and recency in a wide range of situations. Information is given of similar types of neuronal responses in anatomically related brain regions and what may be deduced about the operation of the recognition memory system. The possibility is discussed that the neuronal responses that signal information concerning the recent occurrence of stimuli may contribute to repetition priming as well as recognition memory. Other described changes in the activity of individual neurones such as response enhancements, or sustained (delay) activity may allow solution of specialised forms of recognition memory tasks where relatively short-term working memory is adequate. Implications of the multi-faceted nature of recognition memory for the interpretation of results are emphasised. Unsolved problems and avenues for future experimentation, including determining the nature of possible underlying synaptic plastic changes, are discussed.

Animals↗