Nothing in Biology Makes Sense except in the Light of Evolution
“Seen in the light of evolution, biology is, perhaps, intellectually the most satisfying and inspiring science. Without that light, it becomes a pile of sundry facts some of them interesting or curious, but making no meaningful picture as a whole.”
A structural equation model indicates that increasing enrollment in baccalaureate-level programs, exposure to college-level science courses, a declining level of religious fundamentalism, and a rising level of civic scientific literacy are responsible for the increased level of public acceptance.
An animal with a nerve “net”
Cephalopods have “intelligent arms”
(Arendt, Tosches, & Marlow, 2016)
Figure 1: Animal phylogeny. A simplified animal phylogenetic tree (showing the evolutionary history of animals), in which lines represent evolutionary diversification. The lengths of the lines are arbitrary, as they do not indicate evolutionary distance. For a brief characterization of the Anthozoa, Bilateria, Ceriantharia, Cnidaria, Ctenophora, Medusozoa and Neuralia, see the glossary. The phylogenetic position of the Ctenophora is not settled, as indicated by a question mark. The Ctenophora image is adapted with permission from Ref. 43, Wiley. The Porifera and Placozoa images are reprinted with permission from Ref. 139 (Nielsen, C. Animal Evolution: Interrelationships of the Living Phyla p31 and p39 (2012)) by the permission of Oxford University Press. The Annelida image is adapted with permission from Ref. 140, Schweizerbart Science Publishers (www.schweizerbart.de).
Figure 2: Comparison of neurodevelopment in the frog, annelid and sea anemone. The frog Xenopus laevis (part a), the annelid Platynereis dumerilii (part b) and the cnidarian Nematostella vectensis (part c) are depicted in their gastrula-like stages (gastrula, trochophora and planula, respectively; upper panels), intermediate developmental (neurula, metatrochophora and late planula, respectively; middle panels) and juvenile stages (tadpole, nectochaete and polyp, respectively; lower panels). Colours demarcate developmental neurogenic regions, and double-headed arrows show the apical (AP)–blastoporal (BL) axis. All views in parts a–c are lateral. At gastrula stages (upper panels), blastoporal ectodermal tissue (around the closing blastopore; red) and apical pole ectodermal tissue (violet) can be distinguished. At subsequent stages, a large part of the ectoderm — incluing the former apical and blastoporal regions — gives rise to neurogenic tissue. The neurogenic tissue comprises regions of distinct molecular identity (indicated by different colours), which will give rise to different parts of the nervous system. In the frog (part a), the neural plate (violet, red and yellow) comprises future forebrain tissue, as well as medial and lateral neural tube tissue; it is laterally bounded by developing peripheral nervous system components (blue). Similar regions are apparent in the annelid (part b), and these give rise to the brain, medial and lateral nerve cord and peripheral nervous system. As reasoned in this article, these regions also exist in the cnidarian (part c). In the frog and annelid worm, these regions are further subdivided into specific subregions by the activity of molecular organizing signals15.
Structural measure | Non-human comparison | Human |
---|---|---|
Cortical gray matter %/tot brain vol | insectivores 25% | 50% |
Cortical gray + white | mice 40% | 80% |
Cerebellar mass | primates, mammals 10-15% | 10-15% |
Take homes
Old story
vs. New story
# of cortical (or in birds, pallidum) neurons predicts “cognition?”
The Human Advantage (Herculano-Houzel, 2016)
A further human advantage
Figure 1. Timeline of Key Human Neurodevelopmental Processes and Functional Milestones
The lineage trees shown provide a simplified view of the relationship between neuroepithelial cells (NE), radial glial cells (RG) and neurons (N), without (a) and with (b) basal progenitors (BP) as cellular intermediates in the generation of neurons. They also show the types of cell division involved.
Radial unit hypothesis
Axon growth cone
Glia migrate, too
“Control” networks
non-“control” networks
The “development” of developmental connectomics
Myelination changes “network” properties
Synaptic rearrangment, myelination change cortical thickness
a, Comparison between DCX expression in HIP and the density of DCX-immunopositive cells in the human dentate gyrus36. b, Comparison between transcriptome-based dendrite development trajectory in DFC and Golgi-method-based growth of basal dendrites of layer 3 (L3) and 5 (L5) pyramidal neurons in the human DFC41. c, Comparison between transcriptome-based synapse development trajectory in DFC and density of DFC synapses calculated using electron microscopy42. For b and c, PC1 for gene expression was plotted against age to represent the developmental trajectory of genes associated with dendrite (b) or synapse (c) development. Independent data sets were centred, scaled and plotted on a logarithmic scale. d, PC1 value for the indicated sets of genes (expressed as percentage of maximum) plotted against age to represent general trends and regional differences in several neurodevelopmental processes in NCX, HIP and CBC.
Major division | Ventricular Landmark | Embryonic Division | Structure |
---|---|---|---|
Forebrain | Lateral | Telencephalon | Cerebral cortex |
Basal ganglia | |||
Hippocampus, amygdala | |||
Third | Diencephalon | Thalamus | |
Hypothalamus | |||
Midbrain | Cerebral Aqueduct | Mesencephalon | Tectum, tegmentum |
Hindbrain | 4th | Metencephalon | Cerebellum, pons |
– | Mylencephalon | Medulla oblongata |
Figure 3: Three accounts of the neural basis of an advance in behavioural abilities in infants. a | A maturational view in which the neuroanatomical maturation of one region, in this case the dorsolateral prefrontal cortex (DLPC), allows new behavioural abilities to emerge. Specifically, maturation of DLPC has been associated with successful performance in the object retrieval task (Fig. 1a)50. Note that although the task itself involves activity in several regions, it is thought to be maturation of only one of these, the DLPC, that results in changed behaviour. b | An interactive specialization view in which the onset of a new behavioural ability is due to changes in the interactions between several regions that were already partially active. In this hypothetical illustration, it is suggested that changes in the interactions between DLPC, parietal cortex and cerebellum might give rise to successful performance in the object retrieval paradigm. In contrast to the maturational view, it is refinement of the connectivity between regions, rather than within a single region, that is important. According to this view, regions adjust their functionality together to allow new computations. c | A skill-learning model, in which the pattern of activation of cortical regions changes during the acquisition of new skills throughout the lifespan. In the example illustrated there is decreasing activation of DLPC and medial frontal cortex (pre-supplementary motor area), accompanied by increasing activation of more posterior regions (such as intraparietal sulcus), as human adults perform a visuomotor sequence learning task77. It is suggested that similar changes might occur during the acquisition of new skills by infants. These three accounts are not necessarily mutually exclusive. (Johnson, 2001)