Cognitive map


A cognitive map is a type of mental representation used by an individual to order their personal store of information about their everyday or metaphorical spatial environment, and the relationship of its component parts. The concept was introduced by Edward Tolman in 1948. He tried to explain the behavior of rats that appeared to learn the spatial layout of a maze, and subsequently the concept was applied to other animals, including humans. The term was later generalized by some researchers, especially in the field of operations research, to refer to a kind of semantic network representing an individual's personal knowledge or schemas.

Overview

Cognitive maps have been studied in various fields, such as psychology, education, archaeology, planning, geography, cartography, architecture, landscape architecture, urban planning, management and history. Because of the broad use and study of cognitive maps, it has become a colloquialism for almost any mental representation or model. As a consequence, these mental models are often referred to, variously, as cognitive maps, mental maps, scripts, schemata, and frame of reference.
Cognitive maps serve the construction and accumulation of spatial knowledge, allowing the "mind's eye" to visualize images in order to reduce cognitive load, enhance recall and learning of information. This type of spatial thinking can also be used as a metaphor for non-spatial tasks, where people performing non-spatial tasks involving memory and imaging use spatial knowledge to aid in processing the task. They include information about the spatial relations that objects have among each other in an environment and they help us in orienting and moving in a setting and in space.
The neural correlates of a cognitive map have been speculated to be the place cell system in the hippocampus and the recently discovered grid cells in the entorhinal cortex.

History

The idea of a cognitive map was first developed by Edward C. Tolman. Tolman, one of the early cognitive psychologists, introduced this idea when doing an experiment involving rats and mazes. In Tolman's experiment, a rat was placed in a cross shaped maze and allowed to explore it. After this initial exploration, the rat was placed at one arm of the cross and food was placed at the next arm to the immediate right. The rat was conditioned to this layout and learned to turn right at the intersection in order to get to the food. When placed at different arms of the cross maze however, the rat still went in the correct direction to obtain the food because of the initial cognitive map it had created of the maze. Rather than just deciding to turn right at the intersection no matter what, the rat was able to determine the correct way to the food no matter where in the maze it was placed.
Unfortunately, further research was slowed due to the behaviorist point of view prevalent in the field of psychology at the time. In later years, O'Keefe and Nadel attributed Tolman's research to the hippocampus, stating that it was the key to the rat's mental representation of its surroundings. This observation furthered research in this area and consequently much of hippocampus activity is explained through cognitive map making.
As time went on, the cognitive map was researched in other prospective fields that found it useful, therefore leading to broader and differentiating definitions and applications.

Mental map distinction

A cognitive map is a spatial representation of the outside world that is kept within the mind, until an actual manifestation of this perceived knowledge is generated, a mental map. Cognitive mapping is the implicit, mental mapping the explicit part of the same process. In most cases, a cognitive map exists independently of a mental map, an article covering just cognitive maps would remain limited to theoretical considerations.
Mental mapping is typically associated with landmarks, locations, and geography when demonstrated. Creating mental maps depends on the individual and their perceptions whether they are influenced by media, real-life, or other sources. Because of their factual storage mental maps can be useful when giving directions and navigating. As stated previously this distinction is hard to identify when posed with almost identical definitions, nevertheless there is a distinction.
In some uses, mental map refers to a practice done by urban theorists by having city dwellers draw a map, from memory, of their city or the place they live. This allows the theorist to get a sense of which parts of the city or dwelling are more substantial or imaginable. This, in turn, lends itself to a decisive idea of how well urban planning has been conducted.

Acquisition of the cognitive maps

The cognitive map is generated from a number of sources, both from the visual system and elsewhere. Much of the cognitive map is created through self-generated movement cues. Inputs from senses like vision, proprioception, olfaction, and hearing are all used to deduce a person's location within their environment as they move through it. This allows for path integration, the creation of a vector that represents one's position and direction within one's environment, specifically in comparison to an earlier reference point. This resulting vector can be passed along to the hippocampal place cells where it is interpreted to provide more information about the environment and one's location within the context of the cognitive map.
Directional cues and positional landmarks are also used to create the cognitive map. Within directional cues, both explicit cues, like markings on a compass, as well as gradients, like shading or magnetic fields, are used as inputs to create the cognitive map. Directional cues can be used both statically, when a person does not move within his environment while interpreting it, and dynamically, when movement through a gradient is used to provide information about the nature of the surrounding environment. Positional landmarks provide information about the environment by comparing the relative position of specific objects, whereas directional cues give information about the shape of the environment itself. These landmarks are processed by the hippocampus together to provide a graph of the environment through relative locations.
Alex Siegel and Sheldon White proposed a model of acquisition of spatial knowledge based on different levels. The first stage of the process is said to be limited to the landmarks available in a new environment. Then, as a second stage, information about the routes that connect landmarks will be encoded, at the beginning in a non-metric representation form and consequently they will be expanded with metric properties, such as distances, durations and angular deviations. In the third and final step, the observer will be able to use a survey representation of the surroundings, using an allocentric point of view.
All in all, the acquisition of cognitive maps is a gradual construction. This kind of knowledge is multimodal in nature and it is built up by different pieces of information coming from different sources that are integrated step by step.

Neurological basis

Cognitive mapping is believed to largely be a function of the hippocampus. The hippocampus is connected to the rest of the brain in such a way that it is ideal for integrating both spatial and nonspatial information. Connections from the postrhinal cortex and the medial entorhinal cortex provide spatial information to the hippocampus. Connections from the perirhinal cortex and lateral entorhinal cortex provide nonspatial information. The integration of this information in the hippocampus makes the hippocampus a practical location for cognitive mapping, which necessarily involves combining information about an object's location and its other features.
O'Keefe and Nadel were the first to outline a relationship between the hippocampus and cognitive mapping. Many additional studies have shown additional evidence that supports this conclusion. Specifically, pyramidal cells have been implicated as the neuronal basis for cognitive maps within the hippocampal system.
Numerous studies by O'Keefe have implicated the involvement of place cells. Individual place cells within the hippocampus correspond to separate locations in the environment with the sum of all cells contributing to a single map of an entire environment. The strength of the connections between the cells represents the distances between them in the actual environment. The same cells can be used for constructing several environments, though individual cells' relationships to each other may differ on a map by map basis. The possible involvement of place cells in cognitive mapping has been seen in a number of mammalian species, including rats and macaque monkeys. Additionally, in a study of rats by Manns and Eichenbaum, pyramidal cells from within the hippocampus were also involved in representing object location and object identity, indicating their involvement in the creation of cognitive maps. However, there has been some dispute as to whether such studies of mammalian species indicate the presence of a cognitive map and not another, simpler method of determining one's environment.
While not located in the hippocampus, grid cells from within the medial entorhinal cortex have also been implicated in the process of path integration, actually playing the role of the path integrator while place cells display the output of the information gained through path integration. The results of path integration are then later used by the hippocampus to generate the cognitive map. The cognitive map likely exists on a circuit involving much more than just the hippocampus, even if it is primarily based there. Other than the medial entorhinal cortex, the presubiculum and parietal cortex have also been implicated in the generation of cognitive maps.