The cerebral cortex, also known as the cerebral mantle, is the outer layer of neural tissue of the cerebrum of the brain in humans and other mammals. The cerebral cortex mostly consists of the six-layered neocortex, with just 10% consisting of allocortex. It is separated into two cortices, by the longitudinal fissure that divides the cerebrum into the left and right cerebral hemispheres. The two hemispheres are joined beneath the cortex by the corpus callosum. The cerebral cortex is the largest site of neural integration in the central nervous system. It plays a key role in attention, perception, awareness, thought, memory, language, and consciousness.
Neuropil is any area in the nervous system composed of mostly unmyelinated axons, dendrites and glial cell processes that forms a synaptically dense region containing a relatively low number of cell bodies. The most prevalent anatomical region of neuropil is the brain which, although not completely composed of neuropil, does have the largest and highest synaptically concentrated areas of neuropil in the body. For example, the neocortex and olfactory bulb both contain neuropil.
The limbic system, also known as the paleomammalian cortex, is a set of brain structures located on both sides of the thalamus, immediately beneath the medial temporal lobe of the cerebrum primarily in the forebrain.
A Brodmann area is a region of the cerebral cortex, in the human or other primate brain, defined by its cytoarchitecture, or histological structure and organization of cells.
Proisocortex or pro-isocortex is one of two subtypes of cortical areas in the areas belonging to the neocortex. The other subtype is termed the true isocortex. Proisocortical areas are transitional areas placed between areas of true isocortex and areas of periallocortex. The histological structure of proisocortex is also transitional between true isocortex and either peripaleocortex or periarchicortex, depending on with which subtype of periallocortex the given proisocortical area borders.
The neocortex, also called the neopallium, isocortex, or the six-layered cortex, is a set of layers of the mammalian cerebral cortex involved in higher-order brain functions such as sensory perception, cognition, generation of motor commands, spatial reasoning and language. The neocortex is further subdivided into the true isocortex and the proisocortex.
The triune brain is a model of the evolution of the vertebrate forebrain and behavior, proposed by the American physician and neuroscientist Paul D. MacLean. MacLean originally formulated his model in the 1960s and propounded it at length in his 1990 book The Triune Brain in Evolution. The triune brain consists of the reptilian complex, the paleomammalian complex, and the neomammalian complex (neocortex), viewed each as independently conscious, and as structures sequentially added to the forebrain in the course of evolution. However, this hypothesis has been subject to criticism, and is no longer espoused by the majority of comparative neuroscientists in the post-2000 era.
A cortical column, also called hypercolumn, macrocolumn, functional column or sometimes cortical module, is a group of neurons in the cortex of the brain that can be successively penetrated by a probe inserted perpendicularly to the cortical surface, and which have nearly identical receptive fields. Neurons within a minicolumn (microcolumn) encode similar features, whereas a hypercolumn "denotes a unit containing a full set of values for any given set of receptive field parameters". A cortical module is defined as either synonymous with a hypercolumn (Mountcastle) or as a tissue block of multiple overlapping hypercolumns.
The archicortex, or archipallium, is the phylogenetically oldest region of the brain's cerebral cortex. It is often considered contiguous with the olfactory cortex, but its extent varies among species. In older species, such as fish, the archipallium makes up most of the cerebrum. Amphibians develop an archipallium and paleopallium.
The allocortex or heterogenetic cortex, and neocortex are the two types of cerebral cortex in the brain. The allocortex is the much smaller area of cortex taking up just ten per cent; the neocortex takes up the remaining 90 per cent. It is characterized by having just three or four cortical layers, in contrast with the six layers of the neocortex. There are three subtypes of allocortex: the paleocortex, the archicortex, and the periallocortex – a transitional zone between the neocortex and the allocortex.
The posterior cingulate cortex (PCC) is the caudal part of the cingulate cortex, located posterior to the anterior cingulate cortex. This is the upper part of the "limbic lobe". The cingulate cortex is made up of an area around the midline of the brain. Surrounding areas include the retrosplenial cortex and the precuneus.
The amygdalofugal pathway is one of the three major efferent pathways of the amygdala, meaning that it is one of the three principal pathways by which fibers leave the amygdala. It leads from the basolateral nucleus and central nucleus of the amygdala. The amygdala is a limbic structure in the medial temporal lobe of the brain. The other main efferent pathways from the amygdala are the stria terminalis and anterior commissure.
In anatomy of animals, the paleocortex, or paleopallium, is a region within the telencephalon in the vertebrate brain. This type of cortical tissue consists of three cortical laminae. In comparison, the neocortex has six layers and the archicortex has three or four layers. Because the number of laminae that compose a type of cortical tissue seems to be directly proportional to both the information-processing capabilities of that tissue and its phylogenetic age, paleocortex is thought to be an intermediate between the archicortex and the neocortex in both aspects.
The development of the nervous system in humans, or neural development or neurodevelopment involves the studies of embryology, developmental biology, and neuroscience to describe the cellular and molecular mechanisms by which the complex nervous system forms in humans, develops during prenatal development, and continues to develop postnatally.
The principles that govern the evolution of brain structure are not well understood. Brain to body size scales allometrically. Small bodied mammals have relatively large brains compared to their bodies whereas large mammals have smaller brain to body ratios. If brain weight is plotted against body weight for primates, the regression line of the sample points can indicate the brain power of a primate species. Lemurs for example fall below this line which means that for a primate of equivalent size, we would expect a larger brain size. Humans lie well above the line indicating that humans are more encephalized than lemurs. In fact, humans are more encephalized than all other primates.
In neuroanatomy, pallium refers to the layers of grey and white matter that cover the upper surface of the cerebrum in vertebrates. The non-pallial part of the telencephalon builds the subpallium. In basal vertebrates the pallium is a relatively simple three-layered structure, encompassing 3–4 histogenetically distinct domains, plus the olfactory bulb.
Agranular insula is a portion of the cerebral cortex defined on the basis of internal structure in the human, the macaque, the rat, and the mouse. Classified as allocortex (periallocortex), it is in primates distinguished from adjacent neocortex (proisocortex) by absence of the external granular layer (II) and of the internal granular layer (IV). It occupies the anterior part of the insula, the posterior portion of the orbital gyri and the medial part of the temporal pole. In rodents it is located on the ventrolateral surface of the cortex rostrally, between the piriform area ventrally and the gustatory area or the visceral area dorsally.
Granular insular cortex refers to a portion of the cerebral cortex defined on the basis of internal structure in the human and macaque, the rat, and the mouse. Classified as neocortex, it is in primates distinguished from adjacent allocortex (periallocortex) by the presence of granular layers – external granular layer (II) and internal granular layer (IV) – and by differentiation of the external pyramidal layer (III) into sublayers. In primates it occupies the posterior part of the insula. In rodents it is located on the lateral surface of the cortex rostrally, dorsal to the gustatory area or, more caudally, dorsal to the agranular insula.
Disconnection syndrome is a general term for a collection of neurological symptoms caused -- via lesions to associational or commissural nerve fibres -- by damage to the white matter axons of communication pathways in the cerebrum, independent of any lesions to the cortex. The behavioral effects of such disconnections are relatively predictable in adults. Disconnection syndromes usually reflect circumstances where regions A and B still have their functional specializations except in domains that depend on the interconnections between the two regions.
Mesocortex is the transitional areas of the cerebral cortex, formed at borders between true isocortex and true allocortex. Parts of mesocortex that lie closer to the true isocortex and have more resemblance to the isocortex in their cytoarchitectonics and histology, are called proisocortex. Parts of mesocortex that lie closer to the true allocortex and have more resemblance to the allocortex in their cytoarchitectonics and histology, are called periallocortex.
