Vertebrates
The first vertebrates appeared over 500 million years ago (Mya) during the Cambrian period, and may have resembled the modern jawless fish (hagfish and lamprey) in form. Jawed vertebrates appeared by 445 Mya, tetrapods by 350 Mya, amniotes by 310 Mya and mammaliaforms by 200 Mya (approximately). Each vertebrate clade has an equally long evolutionary history, but the brains of modern fish, amphibians, reptiles, birds and mammals show a gradient of size and complexity that roughly follows the evolutionary sequence. All of these brains contain the same set of basic anatomical structures, but many are rudimentary in the hagfish, whereas in mammals the foremost part (forebrain, especially the telencephalon) is greatly developed and expanded.
Brains are most commonly compared in terms of their mass. The relationship between brain size, body size and other variables has been studied across a wide range of vertebrate species. As a rule of thumb, brain size increases with body size, but not in a simple linear proportion. In general, smaller animals tend to have proportionally larger brains, measured as a fraction of body size. For mammals, the relationship between brain volume and body mass essentially follows a power law with an exponent of about 0.75. This formula describes the central tendency, but every family of mammals departs from it to some degree, in a way that reflects in part the complexity of their behavior. For example, primates have brains 5 to 10 times larger than the formula predicts. Predators, who have to implement various hunting strategies against the ever changing anti-predator adaptations, tend to have larger brains relative to body size than their prey.
All vertebrate brains share a common underlying form, which appears most clearly during early stages of embryonic development. In its earliest form, the brain appears as three vesicular swellings at the front end of the neural tube; these swellings eventually become the forebrain (prosencephalon), midbrain (mesencephalon) and hindbrain (rhombencephalon), respectively. At the earliest stages of brain development, the three areas are roughly equal in size. In many aquatic/semiaquatic vertebrates such as fish and amphibians, the three parts remain similar in size in adults, but in terrestrial tetrapods such as mammals, the forebrain becomes much larger than the other parts, the hindbrain develops a bulky dorsal extension known as the cerebellum, and the midbrain becomes very small as a result.
The brains of vertebrates are made of very soft tissue. Living brain tissue is pinkish on the outside and mostly white on the inside, with subtle variations in color. Vertebrate brains are surrounded by a system of connective tissue membranes called meninges, which separate the skull from the brain. Cerebral arteries pierce the outer two layers of the meninges, the dura and arachnoid mater, into the subarachnoid space and perfuse the brain parenchyma via arterioles perforating into the innermost layer of the meninges, the pia mater. The endothelial cells in the cerebral blood vessel walls are joined tightly to one another, forming the blood–brain barrier, which blocks the passage of many toxins and pathogens (though at the same time blocking antibodies and some drugs, thereby presenting special challenges in treatment of diseases of the brain). As a result of the osmotic restriction by the blood-brain barrier, the metabolites within the brain are cleared mostly by bulk flow of the cerebrospinal fluid within the glymphatic system instead of via venules like other parts of the body.
Neuroanatomists usually divide the vertebrate brain into six main subregions: the telencephalon (the cerebral hemispheres), diencephalon (thalamus and hypothalamus), mesencephalon (midbrain), cerebellum, pons and medulla oblongata, with the midbrain, pons and medulla often collectively called the brainstem. Each of these areas has a complex internal structure. Some parts, such as the cerebral cortex and the cerebellar cortex, are folded into convoluted gyri and sulci in order to maximize surface area within the available intracranial space. Other parts, such as the thalamus and hypothalamus, consist of many small clusters of nuclei known as "ganglia". Thousands of distinguishable areas can be identified within the vertebrate brain based on fine distinctions of neural structure, chemistry, and connectivity.
Although the same basic components are present in all vertebrate brains, some branches of vertebrate evolution have led to substantial distortions of brain geometry, especially in the forebrain area. The brain of a shark shows the basic components in a straightforward way, but in teleost fishes (the great majority of existing fish species), the forebrain has become "everted", like a sock turned inside out. In birds, there are also major changes in forebrain structure. These distortions can make it difficult to match brain components from one species with those of another species.
Here is a list of some of the most important vertebrate brain components, along with a brief description of their functions as currently understood:
The medulla, along with the spinal cord, contains many small nuclei involved in a wide variety of sensory and involuntary motor functions such as vomiting, heart rate and digestive processes.
The pons lies in the brainstem directly above the medulla. Among other things, it contains nuclei that control often voluntary but simple acts such as sleep, respiration, swallowing, bladder function, equilibrium, eye movement, facial expressions, and posture.
The hypothalamus is a small region at the base of the forebrain, whose complexity and importance belies its size. It is composed of numerous small nuclei, each with distinct connections and neurochemistry. The hypothalamus is engaged in additional involuntary or partially voluntary acts such as sleep and wake cycles, eating and drinking, and the release of some hormones.
The thalamus is a collection of nuclei with diverse functions: some are involved in relaying information to and from the cerebral hemispheres, while others are involved in motivation. The subthalamic area (zona incerta) seems to contain action-generating systems for several types of "consummatory" behaviors such as eating, drinking, defecation, and copulation.
The cerebellum modulates the outputs of other brain systems, whether motor-related or thought related, to make them certain and precise. Removal of the cerebellum does not prevent an animal from doing anything in particular, but it makes actions hesitant and clumsy. This precision is not built-in but learned by trial and error. The muscle coordination learned while riding a bicycle is an example of a type of neural plasticity that may take place largely within the cerebellum. 10% of the brain's total volume consists of the cerebellum and 50% of all neurons are held within its structure.
The optic tectum allows actions to be directed toward points in space, most commonly in response to visual input. In mammals, it is usually referred to as the superior colliculus, and its best-studied function is to direct eye movements. It also directs reaching movements and other object-directed actions. It receives strong visual inputs, but also inputs from other senses that are useful in directing actions, such as auditory input in owls and input from the thermosensitive pit organs in snakes. In some primitive fishes, such as lampreys, this region is the largest part of the brain. The superior colliculus is part of the midbrain.
The pallium is a layer of grey matter that lies on the surface of the forebrain and is the most complex and most recent evolutionary development of the brain as an organ. In reptiles and mammals, it is called the cerebral cortex. Multiple functions involve the pallium, including smell and spatial memory. In mammals, where it becomes so large as to dominate the brain, it takes over functions from many other brain areas. In many mammals, the cerebral cortex consists of folded bulges called gyri that create deep furrows or fissures called sulci. The folds increase the surface area of the cortex and therefore increase the amount of gray matter and the amount of information that can be stored and processed.
The hippocampus, strictly speaking, is found only in mammals. However, the area it derives from, the medial pallium, has counterparts in all vertebrates. There is evidence that this part of the brain is involved in complex events such as spatial memory and navigation in fishes, birds, reptiles, and mammals.
The basal ganglia are a group of interconnected structures in the forebrain. The primary function of the basal ganglia appears to be action selection: they send inhibitory signals to all parts of the brain that can generate motor behaviors, and in the right circumstances can release the inhibition, so that the action-generating systems are able to execute their actions. Reward and punishment exert their most important neural effects by altering connections within the basal ganglia.
The olfactory bulb is a special structure that processes olfactory sensory signals and sends its output to the olfactory part of the pallium. It is a major brain component in many vertebrates, but is greatly reduced in humans and other primates (whose senses are dominated by information acquired by sight rather than smell).
Modern reptiles and mammals diverged from a common ancestor around 320 million years ago. The number of extant reptiles far exceeds the number of mammalian species, with 11,733 recognized species of reptiles compared to 5,884 extant mammals. Along with the species diversity, reptiles have diverged in terms of external morphology, from limbless to tetrapod gliders to armored chelonians, reflecting adaptive radiation to a diverse array of environments.
Morphological differences are reflected in the nervous system phenotype, such as: absence of lateral motor column neurons in snakes, which innervate limb muscles controlling limb movements; absence of motor neurons that innervate trunk muscles in tortoises; presence of innervation from the trigeminal nerve to pit organs responsible to infrared detection in snakes. Variation in size, weight, and shape of the brain can be found within reptiles. For instance, crocodilians have the largest brain volume to body weight proportion, followed by turtles, lizards, and snakes. Reptiles vary in the investment in different brain sections. Crocodilians have the largest telencephalon, while snakes have the smallest. Turtles have the largest diencephalon per body weight whereas crocodilians have the smallest. On the other hand, lizards have the largest mesencephalon.
Yet their brains share several characteristics revealed by recent anatomical, molecular, and ontogenetic studies. Vertebrates share the highest levels of similarities during embryological development, controlled by conserved transcription factors and signaling centers, including gene expression, morphological and cell type differentiation. In fact, high levels of transcriptional factors can be found in all areas of the brain in reptiles and mammals, with shared neuronal clusters enlightening brain evolution. Conserved transcription factors elucidate that evolution acted in different areas of the brain by either retaining similar morphology and function, or diversifying it.
Anatomically, the reptilian brain has less subdivisions than the mammalian brain, however it has numerous conserved aspects including the organization of the spinal cord and cranial nerve, as well as elaborated brain pattern of organization. Elaborated brains are characterized by migrated neuronal cell bodies away from the periventricular matrix, region of neuronal development, forming organized nuclear groups. Aside from reptiles and mammals, other vertebrates with elaborated brains include hagfish, galeomorph sharks, skates, rays, teleosts, and birds. Overall elaborated brains are subdivided in forebrain, midbrain, and hindbrain.
The hindbrain coordinates and integrates sensory and motor inputs and outputs responsible for, but not limited to, walking, swimming, or flying. It contains input and output axons interconnecting the spinal cord, midbrain and forebrain transmitting information from the external and internal environments. The midbrain links sensory, motor, and integrative components received from the hindbrain, connecting it to the forebrain. The tectum, which includes the optic tectum and torus semicircularis, receives auditory, visual, and somatosensory inputs, forming integrated maps of the sensory and visual space around the animal. The tegmentum receives incoming sensory information and forwards motor responses to and from the forebrain. The isthmus connects the hindbrain with midbrain. The forebrain region is particularly well developed, is further divided into diencephalon and telencephalon. Diencephalon is related to regulation of eye and body movement in response to visual stimuli, sensory information, circadian rhythms, olfactory input, and autonomic nervous system. Telencephalon is related to control of movements, neurotransmitters and neuromodulators responsible for integrating inputs and transmitting outputs are present, sensory systems, and cognitive functions.
The most obvious difference between the brains of mammals and other vertebrates is their size. On average, a mammal has a brain roughly twice as large as that of a bird of the same body size, and ten times as large as that of a reptile of the same body size.
Size, however, is not the only difference: there are also substantial differences in shape. The hindbrain and midbrain of mammals are generally similar to those of other vertebrates, but dramatic differences appear in the forebrain, which is greatly enlarged and also altered in structure. The cerebral cortex is the part of the brain that most strongly distinguishes mammals. In non-mammalian vertebrates, the surface of the cerebrum is lined with a comparatively simple three-layered structure called the pallium. In mammals, the pallium evolves into a complex six-layered structure called neocortex or isocortex. Several areas at the edge of the neocortex, including the hippocampus and amygdala, are also much more extensively developed in mammals than in other vertebrates.
The elaboration of the cerebral cortex carries with it changes to other brain areas. The superior colliculus, which plays a major role in visual control of behavior in most vertebrates, shrinks to a small size in mammals, and many of its functions are taken over by visual areas of the cerebral cortex. The cerebellum of mammals contains a large portion (the neocerebellum) dedicated to supporting the cerebral cortex, which has no counterpart in other vertebrates.
In placentals, there is a wide nerve tract connecting the cerebral hemispheres called the corpus callosum.
The brains of humans and other primates contain the same structures as the brains of other mammals, but are generally larger in proportion to body size. The encephalization quotient (EQ) is used to compare brain sizes across species. It takes into account the nonlinearity of the brain-to-body relationship. Humans have an average EQ in the 7-to-8 range, while most other primates have an EQ in the 2-to-3 range. Dolphins have values higher than those of primates other than humans, but nearly all other mammals have EQ values that are substantially lower.
Most of the enlargement of the primate brain comes from a massive expansion of the cerebral cortex, especially the prefrontal cortex and the parts of the cortex involved in vision. The visual processing network of primates includes at least 30 distinguishable brain areas, with a complex web of interconnections. It has been estimated that visual processing areas occupy more than half of the total surface of the primate neocortex. The prefrontal cortex carries out functions that include planning, working memory, motivation, attention, and executive control. It takes up a much larger proportion of the brain for primates than for other species, and an especially large fraction of the human brain.
