Memory

For other uses, see Memory (disambiguation).
Overview of the forms and functions of memory in the sciences

Memory is the process in which information is encoded, stored, and retrieved. Encoding allows information from the outside world to be sensed in the form of chemical and physical stimuli. In the first stage the information must be changed so that it may be put into the encoding process. Storage is the second memory stage or process. This entails that information is maintained over short periods of time. Finally the third process is the retrieval of information that has been stored. Such information must be located and returned to the consciousness. Some retrieval attempts may be effortless due to the type of information, and other attempts to remember stored information may be more demanding for various reasons.

From an information processing perspective there are three main stages in the formation and retrieval of memory:

The loss of memory is described as forgetfulness.

Sensory

Main article: Sensory memory

Sensory memory holds sensory information less than one second after an item is perceived. The ability to look at an item and remember what it looked like with just a split second of observation, or memorization, is the example of sensory memory. It is out of cognitive control and is an automatic response. With very short presentations, participants often report that they seem to "see" more than they can actually report. The first experiments exploring this form of sensory memory were precisely conducted by George Sperling (1963)[1] using the "partial report paradigm". Subjects were presented with a grid of 12 letters, arranged into three rows of four. After a brief presentation, subjects were then played either a high, medium or low tone, cuing them which of the rows to report. Based on these partial report experiments,Sperling was able to show that the capacity of sensory memory was approximately 12 items, but that it degraded very quickly (within a few hundred milliseconds). Because this form of memory degrades so quickly, participants would see the display but be unable to report all of the items (12 in the "whole report" procedure) before they decayed. This type of memory cannot be prolonged via rehearsal.

Three types of sensory memories exist. Iconic memory is a fast decaying store of visual information; a type of sensory memory that briefly stores an image which has been perceived for a small duration. Echoic memory is a fast decaying store of auditory information, another type of sensory memory that briefly stores sounds that have been perceived for short durations.[2] Haptic memory is a type of sensory memory that represents a database for touch stimuli.

Short-term

Main article: Short-term memory

Short-term memory is also known as working memory. Short-term memory allows recall for a period of several seconds to a minute without rehearsal. Its capacity is also very limited: George A. Miller (1956), when working at Bell Laboratories, conducted experiments showing that the store of short-term memory was 7±2 items (the title of his famous paper, "The magical number 7±2"). Modern estimates of the capacity of short-term memory are lower, typically of the order of 4–5 items;[3] however, memory capacity can be increased through a process called chunking.[4] For example, in recalling a ten-digit telephone number, a person could chunk the digits into three groups: first, the area code (such as 123), then a three-digit chunk (456) and lastly a four-digit chunk (7890). This method of remembering telephone numbers is far more effective than attempting to remember a string of 10 digits; this is because we are able to chunk the information into meaningful groups of numbers. This may be reflected in some countries in the tendency to display telephone numbers as several chunks of two to four numbers.

Short-term memory is believed to rely mostly on an acoustic code for storing information, and to a lesser extent a visual code. Conrad (1964)[5] found that test subjects had more difficulty recalling collections of letters that were acoustically similar (e.g. E, P, D). Confusion with recalling acoustically similar letters rather than visually similar letters implies that the letters were encoded acoustically. Conrad's (1964) study, however, deals with the encoding of written text; thus, while memory of written language may rely on acoustic components, generalisations to all forms of memory cannot be made.

Long-term

Olin Levi Warner, Memory (1896). Library of Congress Thomas Jefferson Building, Washington, D.C.
Main article: Long-term memory

The storage in sensory memory and short-term memory generally has a strictly limited capacity and duration, which means that information is not retained indefinitely. By contrast, long-term memory can store much larger quantities of information for potentially unlimited duration (sometimes a whole life span). Its capacity is immeasurable. For example, given a random seven-digit number we may remember it for only a few seconds before forgetting, suggesting it was stored in our short-term memory. On the other hand, we can remember telephone numbers for many years through repetition; this information is said to be stored in long-term memory.

While short-term memory encodes information acoustically, long-term memory encodes it semantically: Baddeley (1966)[6] discovered that, after 20 minutes, test subjects had the most difficulty recalling a collection of words that had similar meanings (e.g. big, large, great, huge) long-term. Another part of long-term memory is episodic memory, "which attempts to capture information such as 'what', 'when' and 'where'".[7] With episodic memory, individuals are able to recall specific events such as birthday parties and weddings.

Short-term memory is supported by transient patterns of neuronal communication, dependent on regions of the frontal lobe (especially dorsolateral prefrontal cortex) and the parietal lobe. Long-term memory, on the other hand, is maintained by more stable and permanent changes in neural connections widely spread throughout the brain. The hippocampus is essential (for learning new information) to the consolidation of information from short-term to long-term memory, although it does not seem to store information itself. Without the hippocampus, new memories are unable to be stored into long-term memory, as learned from patient Henry Molaison after removal of both his hippocampi,[8] and there will be a very short attention span. Furthermore, it may be involved in changing neural connections for a period of three months or more after the initial learning.

Research has suggested that long-term memory storage in humans may be maintained by DNA methylation,[9] or prions.[10]

Models

Models of memory provide abstract representations of how memory is believed to work. Below are several models proposed over the years by various psychologists. Controversy is involved as to whether several memory structures exist.

Atkinson–Shiffrin

The multi-store model (also known as Atkinson–Shiffrin memory model) was first described in 1968 by Atkinson and Shiffrin.

The multi-store model has been criticised for being too simplistic. For instance, long-term memory is believed to be actually made up of multiple subcomponents, such as episodic and procedural memory. It also proposes that rehearsal is the only mechanism by which information eventually reaches long-term storage, but evidence shows us capable of remembering things without rehearsal.

The model also shows all the memory stores as being a single unit whereas research into this shows differently. For example, short-term memory can be broken up into different units such as visual information and acoustic information. In a study by Zlonoga and Gerber (1986), patient 'KF' demonstrated certain deviations from the Atkinson–Shiffrin model. Patient KF was brain damaged, displaying difficulties regarding short-term memory. Recognition of sounds such as spoken numbers, letters, words and easily identifiable noises (such as doorbells and cats meowing) were all impacted. Interestingly, visual short-term memory was unaffected, suggesting a dichotomy between visual and audial memory.[11]

Working

Main article: Working memory

In 1974 Baddeley and Hitch proposed a "working memory model" that replaced the general concept of short-term memory with an active maintenance of information in the short-term storage. In this model, working memory consists of three basic stores: the central executive, the phonological loop and the visuo-spatial sketchpad. In 2000 this model was expanded with the multimodal episodic buffer (Baddeley's model of working memory).[12]

The central executive essentially acts as an attention sensory store. It channels information to the three component processes: the phonological loop, the visuo-spatial sketchpad, and the episodic buffer.

The phonological loop stores auditory information by silently rehearsing sounds or words in a continuous loop: the articulatory process (for example the repetition of a telephone number over and over again). A short list of data is easier to remember.

The visuospatial sketchpad stores visual and spatial information. It is engaged when performing spatial tasks (such as judging distances) or visual ones (such as counting the windows on a house or imagining images).

The episodic buffer is dedicated to linking information across domains to form integrated units of visual, spatial, and verbal information and chronological ordering (e.g., the memory of a story or a movie scene). The episodic buffer is also assumed to have links to long-term memory and semantical meaning.

The working memory model explains many practical observations, such as why it is easier to do two different tasks (one verbal and one visual) than two similar tasks (e.g., two visual), and the aforementioned word-length effect. However, the concept of a central executive as noted here has been criticised as inadequate and vague. Working memory is also the premise for what allows us to do everyday activities involving thought. It is the section of memory where we carry out thought processes and use them to learn and reason about topics.[12]

Types

Researchers distinguish between recognition and recall memory. Recognition memory tasks require individuals to indicate whether they have encountered a stimulus (such as a picture or a word) before. Recall memory tasks require participants to retrieve previously learned information. For example, individuals might be asked to produce a series of actions they have seen before or to say a list of words they have heard before.

By information type

Topographic memory involves the ability to orient oneself in space, to recognize and follow an itinerary, or to recognize familiar places.[13] Getting lost when traveling alone is an example of the failure of topographic memory.[14]

Flashbulb memories are clear episodic memories of unique and highly emotional events.[15] People remembering where they were or what they were doing when they first heard the news of President Kennedy’s assassination,[16] the Sydney Siege or of 9/11 are examples of flashbulb memories.

Anderson (1976)[17] divides long-term memory into declarative (explicit) and procedural (implicit) memories.

Declarative

Main article: Declarative memory

Declarative memory requires conscious recall, in that some conscious process must call back the information. It is sometimes called explicit memory, since it consists of information that is explicitly stored and retrieved.

Declarative memory can be further sub-divided into semantic memory, concerning principles and facts taken independent of context; and episodic memory, concerning information specific to a particular context, such as a time and place. Semantic memory allows the encoding of abstract knowledge about the world, such as "Paris is the capital of France". Episodic memory, on the other hand, is used for more personal memories, such as the sensations, emotions, and personal associations of a particular place or time. Episodic memories often reflect the "firsts" in life such as a first kiss, first day of school or first time winning a championship. These are key events in one's life that can be remembered clearly. Autobiographical memory - memory for particular events within one's own life - is generally viewed as either equivalent to, or a subset of, episodic memory. Visual memory is part of memory preserving some characteristics of our senses pertaining to visual experience. One is able to place in memory information that resembles objects, places, animals or people in sort of a mental image. Visual memory can result in priming and it is assumed some kind of perceptual representational system underlies this phenomenon.

Procedural

In contrast, procedural memory (or implicit memory) is not based on the conscious recall of information, but on implicit learning. It can best be summarized as remember how to do something. Procedural memory is primarily employed in learning motor skills and should be considered a subset of implicit memory. It is revealed when one does better in a given task due only to repetition - no new explicit memories have been formed, but one is unconsciously accessing aspects of those previous experiences. Procedural memory involved in motor learning depends on the cerebellum and basal ganglia.

A characteristic of procedural memory is that the things remembered are automatically translated into actions, and thus sometimes difficult to describe. Some examples of procedural memory include the ability to ride a bike or tie shoelaces.[18]

By temporal direction

Another major way to distinguish different memory functions is whether the content to be remembered is in the past, retrospective memory, or in the future, prospective memory. Thus, retrospective memory as a category includes semantic, episodic and autobiographical memory. In contrast, prospective memory is memory for future intentions, or remembering to remember (Winograd, 1988). Prospective memory can be further broken down into event- and time-based prospective remembering. Time-based prospective memories are triggered by a time-cue, such as going to the doctor (action) at 4pm (cue). Event-based prospective memories are intentions triggered by cues, such as remembering to post a letter (action) after seeing a mailbox (cue). Cues do not need to be related to the action (as the mailbox/letter example), and lists, sticky-notes, knotted handkerchiefs, or string around the finger all exemplify cues that people use as strategies to enhance prospective memory.

Study techniques

To assess infants

Infants do not have the language ability to report on their memories and so verbal reports cannot be used to assess very young children’s memory. Throughout the years, however, researchers have adapted and developed a number of measures for assessing both infants’ recognition memory and their recall memory. Habituation and operant conditioning techniques have been used to assess infants’ recognition memory and the deferred and elicited imitation techniques have been used to assess infants’ recall memory.

Techniques used to assess infants’ recognition memory include the following:

Techniques used to assess infants’ recall memory include the following:

To assess older children and adults

Researchers use a variety of tasks to assess older children and adults' memory. Some examples are:

Failures

Physiology

Brain areas involved in the neuroanatomy of memory such as the hippocampus, the amygdala, the striatum, or the mammillary bodies are thought to be involved in specific types of memory. For example, the hippocampus is believed to be involved in spatial learning and declarative learning, while the amygdala is thought to be involved in emotional memory.[32] Damage to certain areas in patients and animal models and subsequent memory deficits is a primary source of information. However, rather than implicating a specific area, it could be that damage to adjacent areas, or to a pathway traveling through the area is actually responsible for the observed deficit. Further, it is not sufficient to describe memory, and its counterpart, learning, as solely dependent on specific brain regions. Learning and memory are attributed to changes in neuronal synapses, thought to be mediated by long-term potentiation and long-term depression.

In general, the more emotionally charged an event or experience is, the better it is remembered; this phenomenon is known as the memory enhancement effect. Patients with amygdala damage, however, do not show a memory enhancement effect.[33][34]

Hebb distinguished between short-term and long-term memory. He postulated that any memory that stayed in short-term storage for a long enough time would be consolidated into a long-term memory. Later research showed this to be false. Research has shown that direct injections of cortisol or epinephrine help the storage of recent experiences. This is also true for stimulation of the amygdala. This proves that excitement enhances memory by the stimulation of hormones that affect the amygdala. Excessive or prolonged stress (with prolonged cortisol) may hurt memory storage. Patients with amygdalar damage are no more likely to remember emotionally charged words than nonemotionally charged ones. The hippocampus is important for explicit memory. The hippocampus is also important for memory consolidation. The hippocampus receives input from different parts of the cortex and sends its output out to different parts of the brain also. The input comes from secondary and tertiary sensory areas that have processed the information a lot already. Hippocampal damage may also cause memory loss and problems with memory storage.[35] This memory loss includes, retrograde amnesia which is the loss of memory for events that occurred shortly before the time of brain damage.[31]

Cognitive neuroscience

Cognitive neuroscientists consider memory as the retention, reactivation, and reconstruction of the experience-independent internal representation. The term of internal representation implies that such definition of memory contains two components: the expression of memory at the behavioral or conscious level, and the underpinning physical neural changes (Dudai 2007). The latter component is also called engram or memory traces (Semon 1904). Some neuroscientists and psychologists mistakenly equate the concept of engram and memory, broadly conceiving all persisting after-effects of experiences as memory; others argue against this notion that memory does not exist until it is revealed in behavior or thought (Moscovitch 2007).

One question that is crucial in cognitive neuroscience is how information and mental experiences are coded and represented in the brain. Scientists have gained much knowledge about the neuronal codes from the studies of plasticity, but most of such research has been focused on simple learning in simple neuronal circuits; it is considerably less clear about the neuronal changes involved in more complex examples of memory, particularly declarative memory that requires the storage of facts and events (Byrne 2007). Convergence-divergence zones might be the neural networks where memories are stored and retrieved. Considering that there are several kinds of memory, depending on types of represented knowledge, underlying mechanisms, processes functions and modes of acquisition, it is likely that different brain areas support different memory systems and that they are in mutual relationships in neuronal networks: “components of memory representation are distributed widely across different parts of the brain as mediated by multiple neocortical circuits.” [36]

Genetics

Study of the genetics of human memory is in its infancy. A notable initial success was the association of APOE with memory dysfunction in Alzheimer's Disease. The search for genes associated with normally varying memory continues. One of the first candidates for normal variation in memory is the gene KIBRA,[37] which appears to be associated with the rate at which material is forgotten over a delay period.

In infancy

For the inability of adults to retrieve early memories, see Childhood amnesia.

Up until the middle of the 1980s it was assumed that infants could not encode, retain, and retrieve information.[38] A growing body of research now indicates that infants as young as 6-months can recall information after a 24-hour delay.[39] Furthermore, research has revealed that as infants grow older they can store information for longer periods of time; 6-month-olds can recall information after a 24-hour period, 9-month-olds after up to five weeks, and 20-month-olds after as long as twelve months.[40] In addition, studies have shown that with age, infants can store information faster. Whereas 14-month-olds can recall a three-step sequence after being exposed to it once, 6-month-olds need approximately six exposures in order to be able to remember it.[23][39]

It should be noted that although 6-month-olds can recall information over the short-term, they have difficulty recalling the temporal order of information. It is only by 9 months of age that infants can recall the actions of a two-step sequence in the correct temporal order - that is, recalling step 1 and then step 2.[41][42] In other words, when asked to imitate a two-step action sequence (such as putting a toy car in the base and pushing in the plunger to make the toy roll to the other end), 9-month-olds tend to imitate the actions of the sequence in the correct order (step 1 and then step 2). Younger infants (6-month-olds) can only recall one step of a two-step sequence.[39] Researchers have suggested that these age differences are probably due to the fact that the dentate gyrus of the hippocampus and the frontal components of the neural network are not fully developed at the age of 6-months.[24][43][44]

In fact, the term 'infantile amnesia' refers to the phenomenon of accelerated forgetting during infancy. Importantly, infantile amnesia is not unique to humans, and preclinical research (using rodent models) provides insight into the precise neurobiology of this phenomenon. A review of the literature from behavioral neuroscientist Dr Jee Hyun Kim suggests that accelerated forgetting during early life is at least partly due to rapid growth of the brain during this period.[45]

Aging

Main article: Memory and aging

One of the key concerns of older adults is the experience of memory loss, especially as it is one of the hallmark symptoms of Alzheimer's disease. However, memory loss is qualitatively different in normal aging from the kind of memory loss associated with a diagnosis of Alzheimer's (Budson & Price, 2005). Research has revealed that individuals’ performance on memory tasks that rely on frontal regions declines with age. Older adults tend to exhibit deficits on tasks that involve knowing the temporal order in which they learned information;[46] source memory tasks that require them to remember the specific circumstances or context in which they learned information;[47] and prospective memory tasks that involve remembering to perform an act at a future time. Older adults can manage their problems with prospective memory by using appointment books, for example.

Effects of physical exercise

Physical exercise, particularly continuous aerobic exercises such as running, cycling and swimming, has many cognitive benefits and effects on the brain. Influences on the brain include increases in neurotransmitter levels, improved oxygen and nutrient delivery, and increased neurogenesis in the hippocampus. The effects of exercise on memory have important implications for improving children's academic performance, maintaining mental abilities in old age, and the prevention and potential cure of neurological diseases.

Disorders

Main article: Memory disorder

Much of the current knowledge of memory has come from studying memory disorders, particularly amnesia. Loss of memory is known as amnesia. Amnesia can result from extensive damage to: (a) the regions of the medial temporal lobe, such as the hippocampus, dentate gyrus, subiculum, amygdala, the parahippocampal, entorhinal, and perirhinal cortices[48] or the (b) midline diencephalic region, specifically the dorsomedial nucleus of the thalamus and the mammillary bodies of the hypothalamus.[49] There are many sorts of amnesia, and by studying their different forms, it has become possible to observe apparent defects in individual sub-systems of the brain's memory systems, and thus hypothesize their function in the normally working brain. Other neurological disorders such as Alzheimer's disease and Parkinson's disease[50] can also affect memory and cognition. Hyperthymesia, or hyperthymesic syndrome, is a disorder that affects an individual's autobiographical memory, essentially meaning that they cannot forget small details that otherwise would not be stored.[51] Korsakoff's syndrome, also known as Korsakoff's psychosis, amnesic-confabulatory syndrome, is an organic brain disease that adversely affects memory by widespread loss or shrinkage of neurons within the prefrontal cortex.[31]

While not a disorder, a common temporary failure of word retrieval from memory is the tip-of-the-tongue phenomenon. Sufferers of Anomic aphasia (also called Nominal aphasia or Anomia), however, do experience the tip-of-the-tongue phenomenon on an ongoing basis due to damage to the frontal and parietal lobes of the brain.

Influencing factors

Interference can hamper memorization and retrieval. There is retroactive interference, when learning new information makes it harder to recall old information[52] and proactive interference, where prior learning disrupts recall of new information. Although interference can lead to forgetting, it is important to keep in mind that there are situations when old information can facilitate learning of new information. Knowing Latin, for instance, can help an individual learn a related language such as French – this phenomenon is known as positive transfer.[53]

Stress

Stress has a significant effect on memory formation and learning. In response to stressful situations, the brain releases hormones and neurotransmitters (ex. glucocorticoids and catecholamines) which affect memory encoding processes in the hippocampus. Behavioural research on animals shows that chronic stress produces adrenal hormones which impact the hippocampal structure in the brains of rats.[54] An experimental study by German cognitive psychologists L. Schwabe and O. Wolf demonstrates how learning under stress also decreases memory recall in humans.[55] In this study, 48 healthy female and male university students participated in either a stress test or a control group. Those randomly assigned to the stress test group had a hand immersed in ice cold water (the reputable SECPT or ‘Socially Evaluated Cold Pressor Test’) for up to three minutes, while being monitored and videotaped. Both the stress and control groups were then presented with 32 words to memorize. Twenty-four hours later, both groups were tested to see how many words they could remember (free recall) as well as how many they could recognize from a larger list of words (recognition performance). The results showed a clear impairment of memory performance in the stress test group, who recalled 30% fewer words than the control group. The researchers suggest that stress experienced during learning distracts people by diverting their attention during the memory encoding process.

However, memory performance can be enhanced when material is linked to the learning context, even when learning occurs under stress. A separate study by cognitive psychologists Schwabe and Wolf shows that when retention testing is done in a context similar to or congruent with the original learning task (i.e., in the same room), memory impairment and the detrimental effects of stress on learning can be attenuated.[56] Seventy-two healthy female and male university students, randomly assigned to the SECPT stress test or to a control group, were asked to remember the locations of 15 pairs of picture cards – a computerized version of the card game "Concentration" or "Memory". The room in which the experiment took place was infused with the scent of vanilla, as odour is a strong cue for memory. Retention testing took place the following day, either in the same room with the vanilla scent again present, or in a different room without the fragrance. The memory performance of subjects who experienced stress during the object-location task decreased significantly when they were tested in an unfamiliar room without the vanilla scent (an incongruent context); however, the memory performance of stressed subjects showed no impairment when they were tested in the original room with the vanilla scent (a congruent context). All participants in the experiment, both stressed and unstressed, performed faster when the learning and retrieval contexts were similar.[57]

This research on the effects of stress on memory may have practical implications for education, for eyewitness testimony and for psychotherapy: students may perform better when tested in their regular classroom rather than an exam room, eyewitnesses may recall details better at the scene of an event than in a courtroom, and persons suffering from post-traumatic stress may improve when helped to situate their memories of a traumatic event in an appropriate context.

Stressful life experiences may be a cause of memory loss as a person ages. Glucocorticoids that are released during stress damage neurons that are located in the hippocampal region of the brain. Therefore, the more stressful situations that someone encounters, the more susceptible they are to memory loss later on. The CA1 neurons found in the hippocampus are destroyed due to glucocorticoids decreasing the release of glucose and the reuptake of glutamate. This high level of extracellular glutamate allow calcium to enter NMDA receptors which in return kills neurons. Stressful life experiences can also cause repression of memories where a person moves an unbearable memory to the unconscious mind.[31] This directly relates to traumatic events in one's past such as kidnappings, being prisoners of war or sexual abuse as a child.

The more long term the exposure to stress is, the more impact it may have. However, short term exposure to stress also causes impairment in memory by interfering with the function of the hippocampus. Research shows that subjects placed in a stressful situation for a short amount of time still have blood glucocorticoid levels that have increased drastically when measured after the exposure is completed. When subjects are asked to complete a learning task after short term exposure they have often difficulties. Prenatal stress also hinders the ability to learn and memorize by disrupting the development of the hippocampus and can lead to unestablished long term potentiation in the offspring of severely stressed parents. Although the stress is applied prenatally, the offspring show increased levels of glucocorticoids when they are subjected to stress later on in life.[58]

Sleep

Making memories occurs through a three-step process, which can be enhanced by sleep. The three steps are as follows:

  1. Acquisition which is the process of storage and retrieval of new information in memory
  2. Consolidation
  3. Recall

Sleep does not affect acquisition or recall while one is awake. Therefore, sleep has the greatest effect on memory consolidation. During sleep, the neural connections in the brain are strengthened. This enhances the brain’s abilities to stabilize and retain memories. There have been several studies which show that sleep improves the retention of memory, as memories are enhanced through active consolidation. System consolidation takes place during slow-wave sleep (SWS).[59] This process implicates that memories are reactivated during sleep, but that the process doesn’t enhance every memory. It also implicates that qualitative changes are made to the memories when they are transferred to long-term store during sleep. When you are sleeping, the hippocampus replays the events of the day for the neocortex. The neocortex then reviews and processes memories, which moves them into long-term memory. When you do not get enough sleep it makes it more difficult to learn as these neural connections are not as strong, resulting in a lower retention rate of memories. Sleep deprivation makes it harder to focus, resulting in inefficient learning.[59] Furthermore, some studies have shown that sleep deprivation can lead to false memories as the memories are not properly transferred to long-term memory. Therefore, it is important to get the proper amount of sleep so that memory can function at the highest level. One of the primary functions of sleep is thought to be the improvement of the consolidation of information, as several studies have demonstrated that memory depends on getting sufficient sleep between training and test.[60] Additionally, data obtained from neuroimaging studies have shown activation patterns in the sleeping brain that mirror those recorded during the learning of tasks from the previous day,[60] suggesting that new memories may be solidified through such rehearsal.[61]

Construction for general manipulation

Although people often think that memory operates like recording equipment, it is not the case. The molecular mechanisms underlying the induction and maintenance of memory are very dynamic and comprise distinct phases covering a time window from seconds to even a lifetime.[62] In fact, research has revealed that our memories are constructed: “current hypotheses suggest that constructive processes allow individuals to simulate and imagine future episodes, happenings, and scenarios. Since the future is not an exact repetition of the past, simulation of future episodes requires a complex system that can draw on the past in a manner that flexibly extracts and recombines elements of previous experiences - a constructive rather than a reproductive system.” [63] People can construct their memories when they encode them and/or when they recall them. To illustrate, consider a classic study conducted by Elizabeth Loftus and John Palmer (1974)[64] in which people were instructed to watch a film of a traffic accident and then asked about what they saw. The researchers found that the people who were asked, "How fast were the cars going when they smashed into each other?" gave higher estimates than those who were asked, "How fast were the cars going when they hit each other?" Furthermore, when asked a week later whether they have seen broken glass in the film, those who had been asked the question with smashed were twice more likely to report that they have seen broken glass than those who had been asked the question with hit. There was no broken glass depicted in the film. Thus, the wording of the questions distorted viewers’ memories of the event. Importantly, the wording of the question led people to construct different memories of the event – those who were asked the question with smashed recalled a more serious car accident than they had actually seen. The findings of this experiment were replicated around the world, and researchers consistently demonstrated that when people were provided with misleading information they tended to misremember, a phenomenon known as the misinformation effect.[65]

Interestingly, research has revealed that asking individuals to repeatedly imagine actions that they have never performed or events that they have never experienced could result in false memories. For instance, Goff and Roediger[66] (1998) asked participants to imagine that they performed an act (e.g., break a toothpick) and then later asked them whether they had done such a thing. Findings revealed that those participants who repeatedly imagined performing such an act were more likely to think that they had actually performed that act during the first session of the experiment. Similarly, Garry and her colleagues (1996)[67] asked college students to report how certain they were that they experienced a number of events as children (e.g., broke a window with their hand) and then two weeks later asked them to imagine four of those events. The researchers found that one-fourth of the students asked to imagine the four events reported that they had actually experienced such events as children. That is, when asked to imagine the events they were more confident that they experienced the events.

Research reported in 2013 revealed that it is possible to artificially stimulate prior memories and artificially implant false memories in mice. Using optogenetics, a team of RIKEN-MIT scientists caused the mice to incorrectly associate a benign environment with a prior unpleasant experience from different surroundings. Some scientists believe that the study may have implications in studying false memory formation in humans, and in treating PTSD and schizophrenia.[68]

Improving

Main article: Improving memory

A UCLA research study published in the June 2006 issue of the American Journal of Geriatric Psychiatry found that people can improve cognitive function and brain efficiency through simple lifestyle changes such as incorporating memory exercises, healthy eating, physical fitness and stress reduction into their daily lives. This study examined 17 subjects, (average age 53) with normal memory performance. Eight subjects were asked to follow a "brain healthy" diet, relaxation, physical, and mental exercise (brain teasers and verbal memory training techniques). After 14 days, they showed greater word fluency (not memory) compared to their baseline performance. No long term follow up was conducted, it is therefore unclear if this intervention has lasting effects on memory.[69]

There are a loosely associated group of mnemonic principles and techniques that can be used to vastly improve memory known as the Art of memory.

The International Longevity Center released in 2001 a report[70] which includes in pages 14–16 recommendations for keeping the mind in good functionality until advanced age. Some of the recommendations are to stay intellectually active through learning, training or reading, to keep physically active so to promote blood circulation to the brain, to socialize, to reduce stress, to keep sleep time regular, to avoid depression or emotional instability and to observe good nutrition.

Memorization is a method of learning that allows an individual to recall information verbatim. Rote learning is the method most often used. Methods of memorizing things have been the subject of much discussion over the years with some writers, such as Cosmos Rossellius using visual alphabets. The spacing effect shows that an individual is more likely to remember a list of items when rehearsal is spaced over an extended period of time. In contrast to this is cramming: an intensive memorization in a short period of time. Also relevant is the Zeigarnik effect which states that people remember uncompleted or interrupted tasks better than completed ones. The so-called Method of loci uses spatial memory to memorize non-spatial information.[71]

Levels of processing

Craik and Lockhart (1972) proposed that it is the method and depth of processing that affects how an experience is stored in memory, rather than rehearsal.

See also

Notes

  1. ↑ Sperling, G (1963). "A Model for Visual Memory Tasks". hfs.sagepub.com 5 (1): 19–31.
  2. ↑ Carlson, Neil R. (2010). Psychology: the science of behavior. Boston, Mass: Allyn & Bacon. ISBN 0-205-68557-9. OCLC 268547522.
  3. ↑ Cowan, N (February 2001). "The magical number 4 in short-term memory: a reconsideration of mental storage capacity" (PDF). Behav Brain Sci 24 (1): 87–114; discussion 114–85. doi:10.1017/S0140525X01003922. PMID 11515286.
  4. ↑ Miller, G.A. (March 1956). "The magical number seven plus or minus two: some limits on our capacity for processing information". Psychol Rev 63 (2): 81–97. doi:10.1037/h0043158. PMID 13310704.
  5. ↑ Conrad, R. (1964). "Acoustic Confusions in Immediate Memory". British Journal of Psychology 55: 75–84. doi:10.1111/j.2044-8295.1964.tb00899.x.
  6. ↑ Baddeley, A. D. (1966). "The influence of acoustic and semantic similarity on long-term memory for word sequences". Quart. J. Exp. Psychol 18 (4): 302–9. doi:10.1080/14640746608400047. PMID 5956072.
  7. ↑ Clayton, N.S.; Dickinson, A. (September 1998). "Episodic-like memory during cache recovery by scrub jays". Nature 395 (6699): 272–4. doi:10.1038/26216. PMID 9751053.
  8. ↑ Scoville W.B., Milner B. (1957). "Loss of Recent Memory After Bilateral Hippocampal Lesions" (PDF). Journal of Nurology, Neurosurgery and Psychiatry 20: 11–21. doi:10.1136/jnnp.20.1.11. PMC 497229. PMID 13406589.
  9. ↑ Miller C, Sweatt J (2007-03-15). "Covalent modification of DNA regulates memory formation". Neuron 53 (6): 857–869. doi:10.1016/j.neuron.2007.02.022. PMID 17359920.
  10. ↑ Papassotiropoulos, Andreas; Wollmer, M. Axel; Aguzzi, Adriano; Hock, Christoph; Nitsch, Roger M.; de Quervain, Dominique J.-F. (2005). "The prion gene is associated with human long-term memory". Human Molecular Genetics (Oxford Journals) 14 (15): 2241–2246. doi:10.1093/hmg/ddi228. PMID 15987701.
  11. ↑ Zlonoga, B.; Gerber, A. (February 1986). "A case from practice (49). Patient: K.F., born 6 May 1930 (bird fancier's lung)". Schweiz. Rundsch. Med. Prax. 75 (7): 171–2. PMID 3952419.
  12. 1 2 Baddeley, A.D. (2000). "The episodic buffer: a new component of working memory?". Trends in Cognitive Science 4 (11): 417–23. doi:10.1016/S1364-6613(00)01538-2. PMID 11058819.
  13. ↑ "IIDRSI: topographic memory loss". Med.univ-rennes1.fr. Retrieved 2012-11-08.
  14. ↑ Aguirre, G.K.; D'Esposito, M. (September 1999). "Topographical disorientation: a synthesis and taxonomy". Brain 122 (9): 1613–28. doi:10.1093/brain/122.9.1613. PMID 10468502.
  15. ↑ T.L. Brink (2008) Psychology: A Student Friendly Approach. "Unit 7: Memory." pp. 120
  16. ↑ Neisser, Ulric (1982). Memory observed: remembering in natural contexts. San Francisco: W.H. Freeman. ISBN 0-7167-1372-1. OCLC 7837605.
  17. ↑ Anderson, John R. (1976). Language, memory, and though. Hillsdale, N.J.: L. Erlbaum Associates. ISBN 978-0-470-15187-7. OCLC 2331424.
  18. ↑ Schacter, Daniel L; Gilbert, Daniel T; Wegner, Daniel M; (2010). Implicit Memory and Explicit Memory. Psychology (New York: Worth Publishers). p. 238. ISBN 1-4292-3719-8. OCLC 755079969.
  19. ↑ Fagan, J.F. (June 1974). "Infant recognition memory: the effects of length of familiarization and type of discrimination task". Child Dev 45 (2): 351–356. PMID 4837713.
  20. ↑ Rovee-Collier, Carolyn (1999). "The Development of Infant Memory" (PDF). Current Directions in Psychological Science 8 (3): 80–85. doi:10.1111/1467-8721.00019. ISSN 0963-7214.
  21. ↑ Rovee-Collier, C.K., Bhatt, R. S. (1993). Ross Vasta, ed. Evidence of long-term retention in infancy. Annals of Child Development 9 (London: Jessica Kingsley Pub). pp. 1–45. ISBN 1-85302-219-5. OCLC 827689578.
  22. ↑ Hartshorn, K.; Rovee-Collier, C.; Gerhardstein, P.; et al. (March 1998). "The ontogeny of long-term memory over the first year-and-a-half of life". Dev Psychobiol 32 (2): 69–89. doi:10.1002/(SICI)1098-2302(199803)32:2<69::AID-DEV1>3.0.CO;2-Q. PMID 9526683.
  23. 1 2 Meltzoff, A.N. (June 1995). "What infant memory tells us about infantile amnesia: long-term recall and deferred imitation". J Exp Child Psychol 59 (3): 497–515. doi:10.1006/jecp.1995.1023. PMC 3629912. PMID 7622990.
  24. 1 2 Bauer, Patricia J. (2002). "Long-Term Recall Memory: Behavioral and Neuro-Developmental Changes in the First 2 Years of Life". Current Directions in Psychological Science 11 (4): 137–141. doi:10.1111/1467-8721.00186. ISSN 0963-7214.
  25. ↑ Bauer, Patricia J. (2007). Remembering the times of our lives: memory in infancy and beyond. Hillsdale, N.J: Lawrence Erlbaum Associates. ISBN 0-8058-5733-8. OCLC 62089961.
  26. ↑ "Paired-associate learning". Encyclopedia Britannica.
  27. ↑ Kesner RP (2013). "A process analysis of the CA3 subregion of the hippocampus". Front Cell Neurosci 7: 78. doi:10.3389/fncel.2013.00078. PMC 3664330. PMID 23750126.
  28. ↑ "Recall (memory)". Encyclopedia Britannica.
  29. ↑ Baddeley, Alan D., "The Psychology of Memory", pages 131-132, Basic Books, Inc., Publishers, New York, 1976, 0-465-06736-0
  30. ↑ "Recognition (memory)". Encyclopedia Britannica.
  31. 1 2 3 4 Kalat, James W. Introduction to Psychology. Canada: Wadsworth Cengage Learning. ISBN 1-133-95660-2.
  32. ↑ LaBar K.S., & Cabeza R. (2006). "Cognitive neuroscience of emotional memory". Nature Reviews Neuroscience 7 (1): 54–64. doi:10.1038/nrn1825.
  33. ↑ Adolphs R., Cahill L., Schul R., & Babinsky R. (1997). "Impaired declarative memory for emotional material following bilateral amygdala damage in humans". Learning & Memory 4: 291–300. doi:10.1101/lm.4.3.291.
  34. ↑ Cahill L.; Babinsky R.; Markowitsch H.J.; McGaugh J.L. (1995). "The amygdala and emotional memory". Nature 377 (6547): 295–296. doi:10.1038/377295a0.
  35. ↑ Kalat, J. W. (2001). Biological psychology (7th ed.). Belmont, CA: Wadsworth Publishing.
  36. ↑ Ofengenden, Tzofit (2014) Memory formation and belief. Dialogues in Philosophy, Mental and Neuro Sciences, 7(2):34-44 http://www.crossingdialogues.com/Ms-A14-03.pdf
  37. ↑ "Gene called Kibra plays an important role in memory". News-medical.net. Retrieved 2012-11-08.
  38. ↑ Teti D.M. (2005). Handbook of research methods in developmental science: New developments in the study of infant memory. San Francisco: Blackwell Publishing.
  39. 1 2 3 Barr R., Dowden A., & Hayne H. (1996). "Developmental changes in deferred imitation by 6- to 24-month-old infants". Infant Behavior and Development 19: 159–170. doi:10.1016/s0163-6383(96)90015-6.
  40. ↑ Bauer P.J. (2004). "Getting explicit memory off the ground: Steps toward construction of a neuro-developmental account of changes in the first two years of life". Developmental Review 24: 347–373. doi:10.1016/j.dr.2004.08.003.
  41. ↑ Bauer, P.J.; Wiebe, S.A.; Carver, L.J.; Waters, J.M.; Nelson, C.A. (November 2003). "Developments in long-term explicit memory late in the first year of life: behavioral and electrophysiological indices". Psychol Sci 14 (6): 629–35. doi:10.1046/j.0956-7976.2003.psci_1476.x. PMID 14629697.
  42. ↑ Carver, L.J.; Bauer, P.J. (March 1999). "When the event is more than the sum of its parts: 9-month-olds' long-term ordered recall". Memory 7 (2): 147–74. doi:10.1080/741944070. PMID 10645377.
  43. ↑ Carver, L.J.; Bauer, P.J. (December 2001). "The dawning of a past: the emergence of long-term explicit memory in infancy". J Exp Psychol Gen 130 (4): 726–45. doi:10.1037/0096-3445.130.4.726. PMID 11757877.
  44. ↑ Cowan, N. (Ed.) (1997). The development of memory in childhood. Hove, East Sussex: Psychology Press.
  45. ↑ Madsen, Heather Bronwyn; Kim, Jee Hyun (2016-02-01). "Ontogeny of memory: An update on 40 years of work on infantile amnesia". Behavioural Brain Research. Developmental Regulation of Memory in Anxiety and Addiction. 298, Part A: 4–14. doi:10.1016/j.bbr.2015.07.030.
  46. ↑ Parkin A.J., Walter B.M., & Hunkin N.M. (1995). "Relationships between normal aging, frontal lobe function, and memory for temporal and spatial information". Neuropsychology 9: 304–312. doi:10.1037/0894-4105.9.3.304.
  47. ↑ McIntyer J.S., & Craik F.I.M. (1987). "Age differences in memory for item and source information". Canadian Journal of Psychology 41: 175–192. doi:10.1037/h0084154.
  48. ↑ Corkin S, Amaral DG, Gonzalez RG, Johnson KA, Hyman, BT (1997). "H.M.’s medial temporal lobe lesion: Findings from magnetic resonance imaging". The Journal of Neuroscience 17: 3964–3979.
  49. ↑ Zola-Morgan S, Suire LR (1993). "Neuroanatomy of memory". Annual Review of Neuroscience 16: 547–563. doi:10.1146/annurev.ne.16.030193.002555. PMID 8460903.
  50. ↑ "Memory of Time May Be Factor in Parkinson's". Columbia.edu. 1996-04-05. Retrieved 2012-11-08.
  51. ↑ Forgetfulness is the Key to a Healthy Mind. New Scientist, February 16. 2008.
  52. ↑ Underwood BJ (1957). "Interference and forgetting". Psychological Review 64: 49–60. doi:10.1037/h0044616.
  53. ↑ Perkins DN, Salomon G (1992). Postlethwaite, T. Neville; Husén, Torsten, eds. Transfer of learning. International Encyclopedia of Education (2 ed.) (Oxford: Pergamon). ISBN 0-08-041046-4. OCLC 749308019.
  54. ↑ Conrad C.D. (2010). "A critical review of chronic stress effects on spatial learning and memory". Progress in Neuro-Psychopharmacology & Biological Psychiatry 34 (5): 742–755. doi:10.1016/j.pnpbp.2009.11.003.
  55. ↑ Schwabe, L.; Wolf, O.T. (2010). "Learning under stress impairs memory formation". Neurobiology of Learning and Memory 93 (2): 183–188. doi:10.1016/j.nlm.2009.09.009.
  56. ↑ Schwabe, L.; Wolf, O.T. (2009). "The context counts: Congruent learning and testing environments prevent memory retrieval impairment following stress". Affective & Behavioral Neuroscience 9 (3): 229–236. doi:10.3758/CABN.9.3.229.
  57. ↑ Schwabe, L.; Bohringer, A.; Wolf, O.T. (2009). "Stress disrupts context-dependent memory". Learning and Memory 16 (2): 110–113. doi:10.1101/lm.1257509.
  58. ↑ Carlson, N. (2013). Physiology of Behavior, eleventh edition. Upper Saddle River, NJ: Pearson.
  59. 1 2 Karriem-Norwood, Varnada. "Sleep Deprivation and Memory Loss". Web MD. Web MD LLC. Retrieved November 20, 2014.
  60. 1 2 Ellenbogen, J.M.; Hulbert, J.C.; Stickgold, R.; Dinges, D.F.; Thompson-Schill, S.L. (July 2006). "Interfering with theories of sleep and memory: sleep, declarative memory, and associative interference" (PDF). Curr. Biol. 16 (13): 1290–4. doi:10.1016/j.cub.2006.05.024. PMID 16824917.
  61. ↑ Alhola, Paula (2007). "Sleep deprivation: Impact on cognitive performance". Neuropsychiatr Dis Treat (Dove Press) 3: 553–67. PMC 2656292. PMID 19300585.
  62. ↑ Schwarzel. M.& Mulluer. U., "Dynamic Memory Networks", "Cellular and Molecular Life Science", 2006
  63. ↑ Ofengenden, Tzofit (2014) Memory formation and belief. Dialogues in Philosophy, Mental and Neuro Sciences, 7(2):34-44 http://www.crossingdialogues.com/Ms-A14-03.pdf
  64. ↑ Loftus EF & Palmer JC (1974). "Reconstruction of automobile destruction: An example of the interaction between language and memory". Journal of Verbal Learning & Verbal Behavior 13: 585–589. doi:10.1016/s0022-5371(74)80011-3.
  65. ↑ Loftus GR (1992). "When a lie becomes memory’s truth: Memory distortion after exposure to misinformation". Current Directions in Psychological Science 1: 121–123. doi:10.1111/1467-8721.ep10769035.
  66. ↑ Goff LM & Roediger HL (1998). "Imagination inflation for action events: Repeated imaginings lead to illusory recollections". Memory and Cognition 26: 20–33. doi:10.3758/bf03211367.
  67. ↑ Garry M, Manning CG, Loftus EF, & Sherman SJ (1996). "Imagination inflation: Imagining a childhood event inflates confidence that it occurred". Psychonomic Bulletin & Review 3: 208–214. doi:10.3758/bf03212420.
  68. ↑ Hogenboom, Melissa (July 25, 2013). "Scientists can implant false memories into mice". BBC News. Retrieved July 26, 2013. ● "A mouse. A laser beam. A manipulated memory." (video) — the scientists' June 2013 TED talk.
  69. ↑ Small, G.W.; Silverman, D.H.; Siddarth, P.; et al. (June 2006). "Effects of a 14-day healthy longevity lifestyle program on cognition and brain function". Am J Geriatr Psychiatry 14 (6): 538–45. doi:10.1097/01.JGP.0000219279.72210.ca. PMID 16731723.
  70. ↑ "International Longevity Center report on memory" (PDF). Retrieved 1 September 2008.
  71. ↑ Henrik Olsson, Leo Poom and Anne Treisman Proceedings of the National Academy of Sciences of the United States of America , Vol. 102, No. 24 (Jun. 14, 2005), pp. 8776-8780

References

  • Alberini C.M. (2005). "Mechanisms of memory stabilization: are consolidation and reconsolidation similar or distinct processes?". Trends in Neuroscience 28: 51–56. doi:10.1016/j.tins.2004.11.001. 
  • Asimov, Isaac (1979). Life and time. New York: Avon Books.
  • Brockmeier Jens (2010). "After the Archive: Remapping memory". Culture & Psychology 16 (1): 5–35. doi:10.1177/1354067X09353212. 
  • Byrne, J. H. (2007) Plasticity: new concepts, new challenges. In: Roediger, H. L., Dudai, Y. and Fitzpatrick S. M., eds. Science of Memory: Concepts. New York: Oxford University Press, pp. 77–82.
  • Chapouthier, Georges, From the search for a molecular code of memory to the role of neurotransmitters: a historical perspective, Neural Plasticity, 2004, 11(3-4), 151-158
  • Conrad C.D. (2010). "A critical review of chronic stress effects on spatial learning and memory. Progress". Neuro-Psychopharmacology & Biological Psychiatry 34 (5): 742–755. doi:10.1016/j.pnpbp.2009.11.003. 
  • Costa-Mattioli, M; et al. (2007). "eIF2α Phosphorylation Bidirectionally Regulates the Switch from Short- to Long-Term Synaptic Plasticity and Memory". Cell 129 (1): 195–206. doi:10.1016/j.cell.2007.01.050. PMID 17418795. 
  • Cowan, Neilson. 1995. Attention and Memory: An Integrated Frame Network. New York:Oxford university Press, pp 167.
  • Craik, FIM & Lockhart, RS. (1972). "Levels of processing: A framework for memory research" Journal of Verbal Learning and Verbal Behavior, Vol.11, No.6, December 1972, Pages 671-684
  • Danziger, Kurt (2008). Marking the mind: A history of memory. Cambridge: Cambridge University Press.
  • Dudai Y (2006). "Reconsolidation: the advantage of being refocused". Current Opinion in Neurobiology 16: 174–178. doi:10.1016/j.conb.2006.03.010. 
  • Dudai, Y. (2007) Memory: It’s all about representations. In: Roediger, H. L., Dudai, Y. and Fitzpatrick S. M., eds. Science of Memory: Concepts. New York: Oxford University Press, pp. 13–16.
  • Eysenck MW, Eysenck MC (1980). "Effects of processing depth, distinctiveness, and word frequency on retention". British Journal of Psychology 71: 263–274. doi:10.1111/j.2044-8295.1980.tb01743.x. 
  • Fivush, Robyn and Neisser, Ulric (1994). The remembering self: Construction and accuracy in the self-narrative. New York: Cambridge University Press.
  • Fransen E., Alonso A.A., Hasselmo M.E. (2002). "simulations of the role of the muscarinic-activated calcium-sensitive non-specific cation current I(NCM) in entorhinal neuronal activity during delayed matching tasks". Journal of Neuroscience 22: 1081–1097. 
  • Jensen O., Lisman J.E. (2005). "Hippocampal sequence-encoding driven by a cortical multi-item working memory buffer". Trends in Neuroscience 28 (2): 67–72. doi:10.1016/j.tins.2004.12.001. 
  • Hacking, I. (1996). Memory science, memory politics. In P. Antze & M. Lambek (Eds.), Tense past: Cultural essays in trauma and memory (pp. 67–87). New York & London: Routledge.
  • LeDoux J.E. (2007) Consolidation: Challenging the traditional view. In: Roediger, H. L., Dudai, Y. and Fitzpatrick S. M., eds. Science of Memory: Concepts. New York: Oxford University Press, pp. 171–175.
  • Mandler, G. (1967). "Organization and memory". In K. W. Spence & J. T. Spence (Eds.), The psychology of learning and motivation: Advances in research and theory. Vol. 1, pp 328–372. New York: Academic Press.
  • Mandler G (2011). "From association to organization". Current Directions in Psychological Science 20 (4): 232–235. doi:10.1177/0963721411414656. 
  • Middleton, David and Brown, Steven (2005). The social psychology of experience: Studies in remembering and forgetting. London: Sage.
  • Moscovitch, M. (2007) Memory: Why the engram is elusive? In: Roediger, H. L., Dudai, Y. and Fitzpatrick S. M., eds. Science of Memory: Concepts. New York: Oxford University Press, pp. 17–21.
  • Nader K., Schafe G.E., LeDoux J.E. (2000b). "The labile nature of consolidation theory". Nature Reviews Neuroscience 1: 216–219. doi:10.1038/35044580. PMID 11257912. 
  • Olick, Jeffrey K., Vered Vinitzky-Seroussi, & Levy, Daniel (Eds.) (2010). The collective memory reader. Oxford University Press.
  • Palmere M., Benton S.L., Glover J.A., Ronning R. (1983). "Elaboration and the recall of main ideas in prose". Journal of Educational Psychology 75: 898–907. doi:10.1037/0022-0663.75.6.898. 
  • Ranganath C., Blumenfeld R.S. (2005). "Doubts about double dissociations between short- and long-term memory". Trends in Cognitive Science 9: 374–380. doi:10.1016/j.tics.2005.06.009. 
  • Russell, Julia; Cardwell, Mike; Flanagan, Cara (2005). Angels on Psychology: Companion Volume. Cheltenham, U.K: Nelson Thornes. ISBN 0-7487-9463-8. 
  • Sara S.J. (2000). "Retrieval and reconsolidation: toward a neurobiology of remembering". Learning and Memory 7: 73–84. doi:10.1101/lm.7.2.73. 
  • Schacter, Daniel L. (2002). The seven sins of memory: How the mind forgets and remembers. Boston: Houghton Mifflin.
  • Schwabe L., Wolf O.T. (2010). "Learning under stress impairs memory formation". Neurobiology of Learning and Memory 93 (2): 183–188. doi:10.1016/j.nlm.2009.09.009. 
  • Schwabe L., Wolf O.T. (2009). "The context counts: Congruent learning and testing environments prevent memory retrieval impairment following stress". Affective & Behavioral Neuroscience 9 (3): 229–236. doi:10.3758/CABN.9.3.229. 
  • Schwabe L., Bohringer A., Wolf O.T. (2009). "Stress disrupts context-dependent memory". Learning and Memory 16 (2): 110–113. doi:10.1101/lm.1257509. 
  • Semon, R. (1904) Die Mneme. Leipzig: Wilhelm Engelmann.
  • Suzuki, W.A. (2007) Working memory: Signals in the brain. In: Roediger, H. L., Dudai, Y. and Fitzpatrick S. M., eds. Science of Memory: Concepts. New York: Oxford University Press, pp. 147–150.
  • Tyler SW, Hertel PT, McCallum MC, Ellis HC (1979). "Cognitive effort and memory". Journal of Experimental Psychology: Human Learning & Memory 5: 607–617. doi:10.1037/0278-7393.5.6.607. 
  • Memory Howard Eichenbaum, Scholarpedia, 3(3):1747. doi:10.4249/scholarpedia.1747

External links

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