with the issue of how remembering and knowing are relatedfficeffice" /> to the amnesic syndrome and whether they are both dependent on the medial temporal lobes. Schacter and Curran (chapter 58) and Curran (chapter 55) also touch on the distinction. The major theoretical point, however, is that here, finally, we have an active area of research aimed at the essence of cognition: Conscious mental experiences that have been changed as a result of earlier experience-induced physical changes in the brain. Other levels and species Concepts such as encoding and retrieval, explicit and implicit memory, or remembering and knowing make TULVING: INTRODUCTION 731 good sense at the level of behavior and cognition of the whole individual, or the whole brain. They are less readily applicable to the study of memory-related events at the level of single neurons, in analyses of the kind described by Goldman-Rakic and associates and Erickson and colleagues in chapters 50 and 51, respectively. Although encoding and retrieval ultimately are rooted in neuronal activity, a single neuron cannot encode or retrieve anything. A neuron may “fire” differentially during the interval between the presentation of the target and the signal for the saccade in the oculomotor working- memory task used by Goldman-Rakic and colleagues, thus providing for a neat neuronal mechanism for holding information “on line” in the short-term memory “store.” But although it is possible to think of this “on-line holding” mechanism as comparable in principle to “holding” information in the long-term “store,” the parallel probably would not work. Retrieval—use of the “stored” information—has different meanings to the organism and is based on rather different operations, in the two situations. Similarly, a neuron may respond differentially to a stimulus when presented for the first time versus the second, as shown by the studies of Erickson and colleagues (chapter 51), and it is tempting to think of the difference as in some sense paralleling novelty versus familiarity detection, or even encoding and retrieval, at the level of the whole brain, but the two levels of analyses are too far apart to allow one to feel confident about such thoughts. A challenging task for neuroscience of memory is to determine to what extent such high-level phenomena as conscious recollection of the occurrence of an event depend on the differential activity of individual units, and to what extent they represent networklevel happenings, or as yet unknown mechanisms, in the brain. Similar thoughts apply to memory in nonhuman animals. A good deal of knowledge about memory, and especially about the neural basis of memory-based behavior, has been derived from work with other animals— nonhuman primates, rodents, birds, and others, all the way to insects, worms, and sea slugs. A major advantage of this work lies in the possibility of a greater range of surgical, chemical, and other material interventions in the normal brain activity. Because memory capabilities, functions, and processes of any two species are always not only similar in some ways but also different in others, some of the methods, findings, and theoretical ideas about human memory have no direct parallels and no direct applicability to nonhuman animals. Thus, there are as yet no known means that could be used to separate implicit from explicit retrieval, or to distinguish between what animals remember and what they know, or what they recollect and what they find merely familiar. Therefore, the important distinctions that shape thought about human memory cannot be transferred forthwith into the study of learning and memory in nonhuman animals. This simple fact also imposes certain limitations on the extent to which the findings from animal studies can be generalized to humans. When these limitations are kept in mind, however, and flat generalizations are avoided, study of memory in one species can be invaluable in providing useful information and offering inspiration to the study of memory in others. The basic structural similarity among the brains of all mammals, especially primates, cannot be gainsaid, and this structural similarity clearly implies some functional similarity as well. The challenging task is to identify exactly wherein the similarities lie. Conclusion This, then, is a brief description of the framework within which much of the neurocognitive research takes place. In one way or another, more or less directly, many empirical findings and most major theoretical ideas and debates involve memory processes, retrieval-related awareness, and memory systems. Study of amnesia and other forms of memory impairments, and theoretical disputes about it, revolve around issues of memory processes, memory awareness, and memory systems. Studies of functional neuroanatomy of memory, made possible by novel techniques such as positron emission tomography (PET) and functional magnetic resonance imaging (fMRI) are focused on memory processes, their interactions with the type of remembered material, and on differences between implicit and explicit retrieval. The outsider who is not familiar with the field should gain some idea from this section about where cognitive neuroscience of memory stands at the turn of the millennium. The insider who knows what the situation was like only 5 years ago, when the first edition of The Cognitive Neurosciences appeared, should find that great changes have occurred since then. New techniques, such as the use of excitotoxic lesions, described by Murray (chapter 52), have produced data that, by past standards, can be regarded as revolutionary. New phenomena, such as “false remembering” discussed and dissected by Schacter and Curran (chapter 58), were not only unknown but also even largely unimaginable 5 years ago. Moreover, most everything that functional neuroimaging techniques (PET and fMRI) have revealed about human memory, as described and analyzed by Buckner (chapter 57), has been discovered in the last 5 years. Stress-related memory impairments and the real possibility that what were thought of as “psychogenic amnesias” have as real a 732 MEMORY physiological basis as “organic amnesias,” discussed by Markowitsch (chapter 54), are newcomers on the memory scene. Even approaches that have been in use for a while, such as psychopharmacology (chapter 55), eventrelated potentials (chapter 56), single-unit recording (chapter 51), and the study of amnesic patients (chapter 53) have yielded new discoveries and fresh insights of a kind that attest genuine progress in the field. These are exciting times in neurocognitive memory research. Happenings at the horizon point to the next 5 years being even more so. [系统提示]: .::本帖子因为[奖励]值得推荐的转帖文章被神经科学论坛管理员a2s2d3实行了:+10金钱 +10经验 的奖惩::. |