Generic bilaterian nervous system Except for a few primitive organisms such as
sponges (which have no nervous system) and
cnidarians (which have a diffuse nervous system consisting of a
nerve net), At a schematic level, that basic worm-shape continues to be reflected in the body and nervous system architecture of all modern bilaterians, including vertebrates. The fundamental bilateral body form is a tube with a hollow gut cavity running from the mouth to the anus, and a nerve cord with an enlargement (a
ganglion) for each body segment, with an especially large ganglion at the front, called the brain. The brain is small and simple in some species, such as
nematode worms; in other species, such as vertebrates, it is a large and very complex organ. There are a few types of existing bilaterians that lack a recognizable brain, including
echinoderms and
tunicates. It has not been definitively established whether the existence of these brainless species indicates that the earliest
bilaterians lacked a brain, or whether their ancestors evolved in a way that led to the disappearance of a previously existing brain structure.
Invertebrates '') have been extensively studied to gain insight into the role of genes in brain development. This category includes
tardigrades,
arthropods,
molluscs, and numerous types of worms. The diversity of invertebrate body plans is matched by an equal diversity in brain structures. Two groups of invertebrates have notably complex brains: arthropods (insects,
crustaceans,
arachnids, and others), and
cephalopods (octopuses,
squids, and similar molluscs). The brains of arthropods and cephalopods arise from twin parallel nerve cords that extend through the body of the animal. Arthropods have a central brain, the
supraesophageal ganglion, with three divisions and large
optical lobes behind each eye for visual processing. There are several invertebrate species whose brains have been studied intensively because they have properties that make them convenient for experimental work: • Fruit flies (
Drosophila), because of the large array of techniques available for studying their
genetics, have been a natural subject for studying the role of genes in brain development. In spite of the large evolutionary distance between insects and mammals, many aspects of
Drosophila neurogenetics have been shown to be relevant to humans. The first biological
clock genes, for example, were identified by examining
Drosophila mutants that showed disrupted daily activity cycles. A search in the genomes of vertebrates revealed a set of analogous genes, which were found to play similar roles in the mouse biological clock—and therefore almost certainly in the human biological clock as well. Studies done on Drosophila, also show that most
neuropil regions of the brain are continuously reorganized throughout life in response to specific living conditions. • The nematode worm
Caenorhabditis elegans, like
Drosophila, has been studied largely because of its importance in genetics. In the early 1970s,
Sydney Brenner chose it as a
model organism for studying the way that genes control development. One of the advantages of working with this worm is that the body plan is very stereotyped: the nervous system of the
hermaphrodite contains exactly 302 neurons, always in the same places, making identical synaptic connections in every worm. Brenner's team sliced worms into thousands of ultrathin sections and photographed each one under an electron microscope, then visually matched fibers from section to section, to map out every neuron and synapse in the entire body. The complete neuronal
wiring diagram of
C.elegans – its
connectome was achieved. Nothing approaching this level of detail is available for any other organism, and the information gained has enabled a multitude of studies that would otherwise have not been possible. • The sea slug
Aplysia californica was chosen by Nobel Prize-winning neurophysiologist
Eric Kandel as a model for studying the cellular basis of
learning and
memory, because of the simplicity and accessibility of its nervous system, and it has been examined in hundreds of experiments.
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. vertebrate brain (left), which later differentiate into structures of the adult brain (right) 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. (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. 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
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. • 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).
Reptiles Comparison of Vertebrate Brains: Mammalian, Reptilian, Amphibian, Teleost, and Ammocoetes.
CB., cerebellum; PT., pituitary body; PN., pineal body; C. STR., corpus striatum; G.H.R., right ganglion habenulæ. I., olfactory; II., optic nerves. 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. 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. 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. Elaborated brains are characterized by migrated neuronal cell bodies away from the periventricular matrix, region of neuronal development, forming organized nuclear groups. 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. In
placentals, there is a wide nerve tract connecting the cerebral hemispheres called the
corpus callosum.
Primates 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. 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. == Development ==