Comparative Neuroanatomy Research Articles

Evolution of the forebrain — revisiting the pallium

Evolution of the forebrain — revisiting the pallium

Neuroanatomy of the vestimentiferan tubeworm Lamellibrachia satsuma provides insights into the evolution of the polychaete nervous system.

Vestimentiferan tubeworms are marine invertebrates that inhabit chemosynthetic environments, and although recent molecular phylogenetic analyses have suggested that vestimentiferan tubeworms are derived from polychaete annelids, they show some morphological features that are different from other polychaetes. For example, vestimentiferans lack a digestive tract and have less body segments and comparative neuroanatomy can provide essential insight into the vestimentiferan body plan and its evolution. In the present study, we investigated the adult nervous system in the vestimentiferan Lamellibrachia satsuma using antibodies against synapsin, serotonin, FMRMamide and acetylated α-tubulin. We also examined the expressions of neural marker genes, elav and synaptotagmin to reveal the distribution of neuronal cell bodies. Brain anatomy shows simple organization in Lamellibrachia compared to other polychaetes. This simplification is probably due to the loss of the digestive tract, passing through the body between the brain and the subesophageal ganglion. In contrast, the ventral nerve cord shows a repeated organizational structure as in the other polychaetes, despite the absence of the multiple segmentation of the trunk. These results suggest that the brain anatomy is variable depending on the function and the condition of surrounding tissues, and that the formation of the rope ladder-like nervous system of the ventral nerve cord is independent from segmentation in polychaetes.

The visual system in the brain of the Bogong moth - A neural substrate for visually guided nocturnal migrations?

Event Abstract Back to Event The visual system in the brain of the Bogong moth - A neural substrate for visually guided nocturnal migrations? Stanley Heinze1* and Eric Warrant1 1 Lund University, Department of Biology, Sweden The Bogong moth (Agrotis infusa) is an Australian moth species that performs spectacular long-distance migrations. Each year in spring, these animals fly southwards for over a thousand kilometers to pinpoint small caves in the mountains of southeastern Australia. After aestivating inside these cool caves, they reverse their migration direction and return northwards to their tropical breeding grounds. Unlike other migratory insects like the monarch butterfly the nocturnal Bogong moth carries out its spectacular behavior during the night. As day-active species use skylight compass cues like the sun and the polarization pattern of the blue sky to guide their migrations, we ask whether the Bogong moth exploits a similar strategy by utilizing visual cues of the nocturnal sky, or has evolved a different mechanism that does not rely on dim skylight cues. To explore the possibility of visually guided migrations in the Bogong moth, we performed immunocytochemical labeling of its brain. Using antibodies against synaptic markers, we were able to describe the general layout of the Bogong moth brain and all its major neuropils. While the overall neuroarchitecture resembles that of other lepidopteran brains, we also observed several distinguishing features: First, the optic lobes (OL) were substantially smaller compared to other migratory insects. Second, the central complex (CX) and its associated lateral accessory lobes were remarkably large with respect to the remaining central brain. As the latter neuropils are involved in processing skylight compass cues in locusts and monarch butterflies, it is tempting to speculate that they have a comparable role in the Bogong moth brain. On the other hand, the underdeveloped OLs might suggest that visual information does not play an equally important role compared to diurnal migrants. The large CX of the Bogong moth combined with its small OLs could imply that other modalities are represented in the CX and used as basis for migratory behavior, or that a large proportion of the OL is devoted to processing skylight compass cues at the expense of other visual information. Comparison to the closely related, but non-migratory A. segetum will help to identify truly unique features of the Bogong moth brain that correlate with its ability to perform nocturnal migrations. Finally, by describing the general layout of the Bogong moth brain, we provide the basis for electrophysiological experiments, opening the way for unraveling the neural basis of nocturnal migrations. Keywords: central complex, nocturnal vision, Migration, Lepidoptera, Comparative Neuroanatomy Conference: International Conference on Invertebrate Vision, Fjälkinge, Sweden, 1 Aug - 8 Aug, 2013. Presentation Type: Poster presentation preferred Topic: Navigation and orientation Citation: Heinze S and Warrant E (2019). The visual system in the brain of the Bogong moth - A neural substrate for visually guided nocturnal migrations?. Front. Physiol. Conference Abstract: International Conference on Invertebrate Vision. doi: 10.3389/conf.fphys.2013.25.00065 Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters. The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated. Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed. For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions. Received: 26 Feb 2013; Published Online: 09 Dec 2019. * Correspondence: Dr. Stanley Heinze, Lund University, Department of Biology, Lund, 22362, Sweden, stanley.heinze@biol.lu.se Login Required This action requires you to be registered with Frontiers and logged in. To register or login click here. Abstract Info Abstract The Authors in Frontiers Stanley Heinze Eric Warrant Google Stanley Heinze Eric Warrant Google Scholar Stanley Heinze Eric Warrant PubMed Stanley Heinze Eric Warrant Related Article in Frontiers Google Scholar PubMed Abstract Close Back to top Javascript is disabled. Please enable Javascript in your browser settings in order to see all the content on this page.

Evolution, development, and plasticity of the human brain: from molecules to bones

Neuroanatomical, molecular, and paleontological evidence is examined in light of human brain evolution. The brain of extant humans differs from the brains of other primates in its overall size and organization, and differences in size and organization of specific cortical areas and subcortical structures implicated into complex cognition and social and emotional processing. The human brain is also characterized by functional lateralizations, reflecting specializations of the cerebral hemispheres in humans for different types of processing, facilitating fast and reliable communication between neural cells in an enlarged brain. The features observed in the adult brain reflect human-specific patterns of brain development. Compared to the brains of other primates, the human brain takes longer to mature, promoting an extended period for establishing cortical microcircuitry and its modifications. Together, these features may underlie the prolonged period of learning and acquisition of technical and social skills necessary for survival, creating a unique cognitive and behavioral niche typical of our species. The neuroanatomical findings are in concordance with molecular analyses, which suggest a trend toward heterochrony in the expression of genes implicated in different functions. These include synaptogenesis, neuronal maturation, and plasticity in humans, mutations in genes implicated in neurite outgrowth and plasticity, and an increased role of regulatory mechanisms, potentially promoting fast modification of neuronal morphologies in response to new computational demands. At the same time, endocranial casts of fossil hominins provide an insight into the timing of the emergence of uniquely human features in the course of evolution. We conclude by proposing several ways of combining comparative neuroanatomy, molecular biology and insights gained from fossil endocasts in future research.

Basicranial Analysis in Young Bovines Reveals a Relation to Breed and Sex

The purpose of this article was to examine the level of sexual dimorphism exhibited in the foramen magnum and occipital condyles of bovine juveniles and to test the utility of three basicranial measurements for estimating sex and to evaluate breed differences. Data were taken from 68 bovines of known sex, age and breed. The linear foramen magnum measurements (breadth and height) were not effective in determining the sex of the skulls, but there appeared differences of the occipital bicondylar breadth between sexes and breeds evaluated ('Bruna dels Pirineus' and others). The occipital bicondylar breadth assigned the sex correctly 75% of the cases. The study of occipital bicondylar breadth could thus be effective to obtain reliable results for the determination of sex in bovine skulls and also could be taken into account when differentiating breeds. It is considered that this study will make morphological contributions to develop a comparative model for other domestic bovine breeds, for there is inadequate literature on foramen magnum morphology for domestic species contrary to the richness of these kinds of studies on humans. The results obtained in this study can also be useful as baseline research data in comparative neuroanatomy and in neuropathology. Focusing on zooarchaeology and also on forensic veterinary, simple morphometric analysis of this type can be used as part of an investigative process prior to more sophisticated and expensive analyses such as the DNA examination.

Will Studies of Macaque Insula Reveal the Neural Mechanisms of Self-Awareness?

The discovery of von Economo neurons within macaque insular cortex by Evrard etal. (2012) described in thisissue of Neuron promises a valuable experimental model to characterize their functional roles. One hypothesis, now open to wider interrogation, is that these intriguing cells mediate self-referential processes underlying or dependent upon consciousness awareness.

PHYLOGENETIC COMPARISON OF NEURON AND GLIA DENSITIES IN THE PRIMARY VISUAL CORTEX AND HIPPOCAMPUS OF CARNIVORES AND PRIMATES

A major focus of comparative neuroanatomy has been on whether the mammalian brain evolves in a concerted or a mosaic fashion. Workers have examined variation in the volume of different brain regions across taxa to test the degree to which selection is constrained by the timing of events in neural development. Whether a conserved neurogenetic program in the mammalian brain constrains the distribution of different cell types, however, has not yet been investigated. Here we tested for evidence of evolutionary constraints on the densities of different cell types in the primary visual cortex (V1) and the hippocampus in 37 primate and 21 carnivore species. Cellular densities in V1 and the hippocampus scale isometrically with respect to one another in carnivores, as predicted by the concerted evolution hypothesis. In primates, however, cellular distributions in the hippocampus and primary visual cortex show no correlations, which supports the hypothesis of mosaic brain evolution. We therefore provide evidence for the presence of constraints controlling the adult densities of different cell types in disparate regions of the mammalian brain, but also for specializations along the primate lineage. We propose that adaptations to modularity at the cellular level may carry a deep phylogenetic signal.

Comparative neuroanatomy of Caudofoveata, Solenogastres, Polyplacophora, and Scaphopoda (Mollusca) and its phylogenetic implications

The nervous system of invertebrates is considered to be a very conservative organ system and thus can be helpful to elucidate questions of phylogenetic relationships. Up to now, comparative neuroanatomical studies have been mainly focused on arthropods, where in-depth studies on major brain structures are abundant. In contrast, except for Gastropoda and Cephalopoda, the nervous system of representatives of the second largest phylum of invertebrates, the Mollusca, is as yet hardly investigated. We therefore initiated an immunohistochemical survey to contribute new neuroanatomical data for several molluscan taxa, especially the lesser known Caudofoveata, Solenogastres, Polyplacophora, and Scaphopoda, focusing on the cellular architecture and distribution of neurotransmitters in the brain. Antisera against the widespread neuroactive substances FMRFamide and serotonin were used to label subsets of neurons. Both antisera were additionally used in combination with acetylated α-tubulin and the nuclear marker DAPI. This enables us to describe the morphology of the nervous system at a fine resolution and to compare its cellular architecture between different species of one taxon, as well as between different taxa of mollusks. On the basis of these results, the nervous system of caudofoveates seems to be most highly derived within the so-called basal (non-conchiferan) mollusks, and a monophyly of a clade Aplacophora could not be confirmed. In general, the brain as well as the remaining nervous system of the molluscan taxa investigated shows a great variability, suggesting a deep time origin of the diversification of this prominent protostome clade.

How to Measure Cortical Folding from MR Images: a Step-by-Step Tutorial to Compute Local Gyrification Index

Cortical folding (gyrification) is determined during the first months of life, so that adverse events occurring during this period leave traces that will be identifiable at any age. As recently reviewed by Mangin and colleagues(2), several methods exist to quantify different characteristics of gyrification. For instance, sulcal morphometry can be used to measure shape descriptors such as the depth, length or indices of inter-hemispheric asymmetry(3). These geometrical properties have the advantage of being easy to interpret. However, sulcal morphometry tightly relies on the accurate identification of a given set of sulci and hence provides a fragmented description of gyrification. A more fine-grained quantification of gyrification can be achieved with curvature-based measurements, where smoothed absolute mean curvature is typically computed at thousands of points over the cortical surface(4). The curvature is however not straightforward to comprehend, as it remains unclear if there is any direct relationship between the curvedness and a biologically meaningful correlate such as cortical volume or surface. To address the diverse issues raised by the measurement of cortical folding, we previously developed an algorithm to quantify local gyrification with an exquisite spatial resolution and of simple interpretation. Our method is inspired of the Gyrification Index(5), a method originally used in comparative neuroanatomy to evaluate the cortical folding differences across species. In our implementation, which we name local Gyrification Index (lGI(1)), we measure the amount of cortex buried within the sulcal folds as compared with the amount of visible cortex in circular regions of interest. Given that the cortex grows primarily through radial expansion(6), our method was specifically designed to identify early defects of cortical development. In this article, we detail the computation of local Gyrification Index, which is now freely distributed as a part of the FreeSurfer Software (http://surfer.nmr.mgh.harvard.edu/, Martinos Center for Biomedical Imaging, Massachusetts General Hospital). FreeSurfer provides a set of automated reconstruction tools of the brain's cortical surface from structural MRI data. The cortical surface extracted in the native space of the images with sub-millimeter accuracy is then further used for the creation of an outer surface, which will serve as a basis for the lGI calculation. A circular region of interest is then delineated on the outer surface, and its corresponding region of interest on the cortical surface is identified using a matching algorithm as described in our validation study(1). This process is repeatedly iterated with largely overlapping regions of interest, resulting in cortical maps of gyrification for subsequent statistical comparisons (Fig. 1). Of note, another measurement of local gyrification with a similar inspiration was proposed by Toro and colleagues(7), where the folding index at each point is computed as the ratio of the cortical area contained in a sphere divided by the area of a disc with the same radius. The two implementations differ in that the one by Toro et al. is based on Euclidian distances and thus considers discontinuous patches of cortical area, whereas ours uses a strict geodesic algorithm and include only the continuous patch of cortical area opening at the brain surface in a circular region of interest.

The standardized central complex of the monarch butterfly brain: a tool for unravelling the neural basis of migratory behavior.

The standardized central complex of the monarch butterfly brain: a tool for unravelling the neural basis of migratory behavior.

Antibodies against conserved amidated neuropeptide epitopes enrich the comparative neurobiology toolbox

BackgroundNeuronal antibodies that show immunoreactivity across a broad range of species are important tools for comparative neuroanatomy. Nonetheless, the current antibody repertoire for non-model invertebrates is limited. Currently, only antibodies against the neuropeptide RFamide and the monoamine transmitter serotonin are extensively used. These antibodies label respective neuron-populations and their axons and dendrites in a large number of species across various animal phyla.ResultsSeveral other neuropeptides also have a broad phyletic distribution among invertebrates, including DLamides, FVamides, FLamides, GWamides and RYamides. These neuropeptides show strong conservation of the two carboxy-terminal amino acids and are α-amidated at their C-termini. We generated and affinity-purified specific polyclonal antibodies against each of these conserved amidated dipeptide motifs. We thoroughly tested antibody reactivity and specificity both by peptide pre-incubation experiments and by showing a close correlation between the immunostaining signals and mRNA expression patterns of the respective precursor genes in the annelid Platynereis. We also demonstrated the usefulness of these antibodies by performing immunostainings on a broad range of invertebrate species, including cnidarians, annelids, molluscs, a bryozoan, and a crustacean. In all species, the antibodies label distinct neuronal populations and their axonal projections. In the ciliated larvae of cnidarians, annelids, molluscs and bryozoans, a subset of antibodies reveal peptidergic innervation of locomotor cilia.ConclusionsWe developed five specific cross-species-reactive antibodies recognizing conserved two-amino-acid amidated neuropeptide epitopes. These antibodies allow specific labelling of peptidergic neurons and their projections in a broad range of invertebrates. Our comparative survey across several marine phyla demonstrates a broad occurrence of peptidergic innervation of larval ciliary bands, suggesting a general role of these neuropeptides in the regulation of ciliary swimming.

Morphological and Quantitative Study of Neurons in the Gracile Nucleus of the Camel Brain Stem

Neurons in the gracile nucleus of the camel brain stem were studied by Golgi method. Neurons were classified based on soma size and shape, density of dendritic tree, morphology and distribution of appendages. Six types of neurons were identified. Type I neurons had very large somata with appendages on their somata and distal dendrites. Type II neurons had large somata and almost smooth dendrites. Type III neurons displayed medium size somata with dendritic appendages of different forms. Type IV neurons were small to medium spheroidal or triangular neurons. Somata and dendrites of these neurons had appendages of different forms. Type V medium-size neurons had bipolar, round or fusiform somata and poorly branching dendritic tree. Some spines and appendages were seen on somata and dendrites of these neurons. Neurons of type VI were medium-size unipolar, round or fusiform with spines on their dendrites. The radiating branching pattern was more common than the tufted for all types of neurons. Wide overlap between widths of dendrites of different orders was found for all neuronal types. Hopefully, this study will improve our understanding of the role of the gracile nucleus as major center for sensory information processing and contribute to our understanding of comparative neuroanatomy and neurophysiology.

Origem e distribuição do nervo femoral do mocó, Kerodon rupestris (Cavidae)

O mocó (Kerodon rupestris Wied,1820), um mamífero roedor da família Cavidae, que se assemelha bastante ao preá, é um animal altamente adaptado às condições de calor e de escassez de água e de alimento, principalmente nos períodos das grandes secas que assolam periodicamente a região do semi-árido nordestino. Verifiica-se que na literatura há escassez de dados referentes à anatomia funcional dos mocós, em especial de trabalhos envolvendo a anatomia do sistema nervoso. Visando conhecer a origem do nervo femoral junto aos forames intervertebrais, sua localização e distribuição pelo membro pélvico, a musculatura envolvida em seu trajeto, a importância desse estudo para clínica de animais silvestres e contribuir para o desenvolvimento da neuroanatomia comparada, procedeu-se esta pesquisa, na qual foram utilizados dez animais adultos de diferentes idades (4 machos e 6 fêmeas) que vieram a óbito no Centro de Multiplicação de Animais Silvestres (Cemas) da Universidade Federal Rural do Semi-Árido (Ufersa). Os animais foram fiixados em solução aquosa de formaldeído a 10% e posteriormente tiveram a cavidade abdominal dissecada até a completa visualização do nervo femoral. Foram verifiicadas variações no número de vértebras lombares nos animais, entre seis (30%) e sete (70%) vértebras, alterando, conseqüentemente, a origem do nervo. No antímero direito, verifiicou-se que em 40% dos animais o nervo femoral originava-se de ramos ventrais de L5L6, em 40% de L5L6L7 e em 20% de L4L5L6. Já no esquerdo 50% dos exemplares o nervo femoral foi formado de raízes ventrais de L5L6, em 30% de L5L6L7 e em 20% de L4L5L6.

Three brain collections for comparative neuroanatomy and neuroimaging

In the context of increasing extinction rates and the potential loss of essential evolutionary biological and anthropological information, it is an important task to support efforts to prepare, preserve, and curate collections of histological brain sections; to disseminate information on such collections in the neuroscience community; and to make the collections publicly available. This review emphasizes the importance of complete, serially sectioned human brains of different ontogenetic stages as well as those of adult and old human individuals for neurobiological and medical research. Such histological sections enable microstructural analyses and anatomical evaluations of functional and structural neuroimaging data, for example, based on magnetic resonance imaging. Here, this review provides the first detailed and updated account of the content of the Stephan, Zilles, and Zilles-Amunts collections, which consist of serially sectioned and cell body- and myelin-stained histological preparations. Finally, this review will give an overview of past and recent research using these collections to increase our understanding of the detailed patterns of divergent brain evolution in primates as well as of the structural organization of the human brain.

The importance of scientific collecting and natural history museums for comparative neuroanatomy

The comparative study of vertebrate brains is inherently dependent upon access to a sufficient number of species and specimens to perform meaningful comparisons. Although many studies rely on compiling published information, continued specimen collection, in addition to more extensive use of existing brain collections and natural history museums, are crucial for detailed neuroanatomical comparisons across species. This review highlights the importance of collecting species through a variety of means, details a marsupial brain collection, and stresses the potential of natural history museums as a resource for comparative neuroanatomy. By taking advantage of as many of these resources as possible, researchers can rapidly increase species coverage and generate a better understanding of how the brain evolves.

A new view of insect–crustacean relationships I. Inferences from neural cladistics and comparative neuroanatomy

Traditional hypotheses regarding the relationships of the major arthropod lineages focus on suites of comparable characters, often those that address features of the exoskeleton. However, because of the enormous morphological variety among arthropods, external characters may lead to ambiguities of interpretation and definition, particularly when species have undergone evolutionary simplification and reversal. Here we present the results of a cladistic analysis using morphological characters associated with brains and central nervous systems, based on the evidence that cerebral organization is generally robust over geological time. Well-resolved, strongly supported phylogenies were obtained from a neuromorphological character set representing a variety of discrete neuroanatomical traits. Phylogenetic hypotheses from this analysis support many accepted relationships, including monophyletic Chelicerata, Myriapoda, and Hexapoda, paraphyletic Crustacea and the union of Hexapoda and Crustacea (Tetraconata). They also support Mandibulata (Myriapoda + Tetraconata). One problematic result, which can be explained by symplesiomorphies that are likely to have evolved in deep time, is the inability to resolve Onychophora as a taxon distinct from Arthropoda. Crucially, neuronal cladistics supports the heterodox conclusion that both Hexapoda and Malacostraca are derived from a common ancestor that possessed a suite of discrete neural centers comprising an elaborate brain. Remipedes and copepods, both resolved as basal to Branchiopoda share a neural ground pattern with Malacostraca. These findings distinguish Hexapoda (Insecta) from Branchiopoda, which is the sister group of the clade Malacostraca + Hexapoda. The present study resolves branchiopod crustaceans as descendents of an ancestor with a complex brain, which means that they have evolved secondary simplification and the loss or reduction of numerous neural systems.

Comparative neuroanatomy suggests repeated reduction of neuroarchitectural complexity in Annelida.

BackgroundPaired mushroom bodies, an unpaired central complex, and bilaterally arranged clusters of olfactory glomeruli are among the most distinctive components of arthropod neuroarchitecture. Mushroom body neuropils, unpaired midline neuropils, and olfactory glomeruli also occur in the brains of some polychaete annelids, showing varying degrees of morphological similarity to their arthropod counterparts. Attempts to elucidate the evolutionary origin of these neuropils and to deduce an ancestral ground pattern of annelid cerebral complexity are impeded by the incomplete knowledge of annelid phylogeny and by a lack of comparative neuroanatomical data for this group. The present account aims to provide new morphological data for a broad range of annelid taxa in order to trace the occurrence and variability of higher brain centers in segmented worms.ResultsImmunohistochemically stained preparations provide comparative neuroanatomical data for representatives from 22 annelid species. The most prominent neuropil structures to be encountered in the annelid brain are the paired mushroom bodies that occur in a number of polychaete taxa. Mushroom bodies can in some cases be demonstrated to be closely associated with clusters of spheroid neuropils reminiscent of arthropod olfactory glomeruli. Less distinctive subcompartments of the annelid brain are unpaired midline neuropils that bear a remote resemblance to similar components in the arthropod brain. The occurrence of higher brain centers such as mushroom bodies, olfactory glomeruli, and unpaired midline neuropils seems to be restricted to errant polychaetes.ConclusionsThe implications of an assumed homology between annelid and arthropod mushroom bodies are discussed in light of the 'new animal phylogeny'. It is concluded that the apparent homology of mushroom bodies in distantly related groups has to be interpreted as a plesiomorphy, pointing towards a considerably complex neuroarchitecture inherited from the last common ancestor, Urbilateria. Within the annelid radiation, the lack of mushroom bodies in certain groups is explained by widespread secondary reductions owing to selective pressures unfavorable for the differentiation of elaborate brains. Evolutionary pathways of mushroom body neuropils in errant polychaetes remain enigmatic.

Cellular configuration of single octopamine neurons in Drosophila

Individual median octopamine neurons in the insect central nervous system serve as an excellent model system for comparative neuroanatomy of single identified cells. The median octopamine cluster of the subesophageal ganglion consists of defined sets of paired and unpaired interneurons, which supply the brain and subesophageal ganglion with extensive ramifications. The developmental program underlying the complex cellular network is unknown. Here we map the segmental location and developmental origins of individual octopamine neurons in the Drosophila subesophageal ganglion. We demonstrate that two sets of unpaired median neurons, located in the mandibular and maxillary segments, exhibit the same projection patterns in the brain. Furthermore, we show that the paired and unpaired neurons belong to distinct lineages. Interspecies comparison of median neurons revealed that many individual octopamine neurons in different species project to equivalent target regions. Such identified neurons with similar morphology can derive from distinct lineages in different species (i.e., paired and unpaired neurons).

The avian nucleus accumbens: parcellation and comparative neuroanatomy

The avian nucleus accumbens: parcellation and comparative neuroanatomy

Evolution of human brain functions: the functional structure of human consciousness

The functional structure of self-aware consciousness in human beings is described based on the evolution of human brain functions. Prior work on heritable temperament and character traits is extended to account for the quantum-like and holographic properties (i.e. parts elicit wholes) of self-aware consciousness. Cladistic analysis is used to identify the succession of ancestors leading to human beings. The functional capacities that emerge along this lineage of ancestors are described. The ecological context in which each cladogenesis occurred is described to illustrate the shifting balance of evolution as a complex adaptive system. Comparative neuroanatomy is reviewed to identify the brain structures and networks that emerged coincident with the emergent brain functions. Individual differences in human temperament traits were well developed in the common ancestor shared by reptiles and humans. Neocortical development in mammals proceeded in five major transitions: from early reptiles to early mammals, early primates, simians, early Homo, and modern Homo sapiens. These transitions provide the foundation for human self-awareness related to sexuality, materiality, emotionality, intellectuality, and spirituality, respectively. The functional structure of human self-aware consciousness is concerned with the regulation of five planes of being: sexuality, materiality, emotionality, intellectuality, and spirituality. Each plane elaborates neocortical functions organized around one of the five special senses. The interactions among these five planes gives rise to a 5 x 5 matrix of subplanes, which are functions that coarsely describe the focus of neocortical regulation. Each of these 25 neocortical functions regulates each of five basic motives or drives that can be measured as temperaments or basic emotions related to fear, anger, disgust, surprise, and happiness/sadness. The resulting 5 x 5 x 5 matrix of human characteristics provides a general and testable model of the functional structure of human consciousness that includes personality, physicality, emotionality, cognition, and spirituality in a unified developmental framework.