Skip to main content

The Quantum Biology of Consciousness and Visual Perception

  • Chapter
  • First Online:
Quantum Biology of the Eye

Abstract

Recently, there has been a lot of interest in the subject of consciousness and its quantum biology properties. Here, we discuss the role of the eye as an important source and participant, in the process of consciousness, and the quantum biology of consciousness. We have discussed the quantum biology of the retina in a process of phototransduction and transfer of information to the brain in the previous chapters. However, we will discuss the role of Müller cells in retina as it participates and facilitates the photon transfer in the inverted retinal thickness. The input of visual information has been recognized as the first step or first “wave” of initiation of the 3-wave processing of consciousness.

The possible link between biology and quantum mechanics as first suggested by Schrödinger in his book “What is Life” has revolutionized the world and created the new field of quantum biology. Quantum biology could explain the process of photon harvesting and electron transfer, different states of excitation and relaxation of electrons, emission of photons, and the generation of ultraweak photon emission (UPE) in the neurons. Also, generation of biophotons, and possibly the process of complex neuronal activity and ultimately the consciousness.

What brings all the chapters of this book together is the suggestion that the quantum effects may underlie the magnetic field effects on the microtubule dynamics. It is the similar mechanism behind magnetoreception in animals, the circadian clocks, Xenon-induced general anesthesia, and the Lithium effect on mania. So here, the old expression “All roads lead to Rome” can be replaced by “All roads to “neuron quantum Biology” lead to “Tryptophan” since it is the Tryptophan molecules that works like an antenna and transfer the electrons and biophotons for a quantum biological task. Due to the fact that all anesthesia-inducing molecules and psychedelic drugs affect tryptophan molecules embedded in tubulin proteins, which are the building blocks of microtubules in neurons, points to the crucial role of this protein in consciousness.

Quantum entanglement may also play a crucial role in brain function and consciousness, particularly the photoemission of singlet oxygen that serves as a quantum messenger to establish long-distance connections that might be essential for consciousness. The role of radical pairs in reorganization of microtubules and generation of biophotons are well recognized, and is an important part in neuronal function, and as the result, the brain function and consciousness.

The fundamental task of the brain as consciousness, is to orchestrate the multiple parallel external events via sensory inputs, combined with the internal cognitive processing to obtain a stable perception of the environment. This is mainly dependent on the perception of conscious sensory experience based on rhythmic sampling of information most effectively by visual input. The process of quantum vision will be discussed with special focus on major components of quantum energy generation in the eye and its transportation to the brain.

It is very interesting to note that nature was able to utilize both classical physics and quantum physics side by side without competition, to combine in order to obtain maximum benefits. It seems that, from photon transfer in retina to neuronal transfer to the brain and interactions in different centers in brain, there are both classic physics, which describe the chemical and electrical modes of communication, and there is quantum mechanical energy transfer via biophotons and vibrational energy transfer, which works hand in hand for optimal results.

Recent studies on primates suggests that various visual cognitive functions exhibit slow rhythmic effects on task performance, which would be supported by low-frequency brain oscillations mainly in the 4–8 Hz frequency range. Alpha brain oscillations (8–12 Hz) play a role in many cognitive functions including visual perception. Alpha oscillation’s amplitude and phase, seem to predict cortical excitability. This will emphasize the significant role of visual input in the process of consciousness since about one-third of the cortical surface in primates brain is involved in visual processing tasks, however, in case of visually impaired or the blind, the plasticity of the brain compensates with rewiring the other sensory inputs instead of optical input to the process of consciousness Kienitz (Eur J Neurosci, 2021).

There would be no such thing as science without conscious minds

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 89.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 119.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Çengel. A concise account of information as meaning ascribed to symbols and its association with conscious mind. Entropy. 2023; https://doi.org/10.3390/e25010177.

  2. University. Central Nervous System. Queensland Brain Institute; 2023. https://qbi.uq.edu.au/brain/brain-anatomy.

    Google Scholar 

  3. Tartu. Morphology of nervous system. Cerebral Cortex. 2023; https://sisu.ut.ee/histology/cerebral-cortex.

  4. Waymire. Neuroscience online. Introduct Neurons Glial Cells. 2023; https://nba.uth.tmc.edu/neuroscience/m/s1/chapter08.html.

  5. Herculano. The remarkable, yet not extraordinary, human brain as a scaled-up primate brain and its associated cost. PNAS. 2012; https://doi.org/10.1073/pnas.1201895109.

  6. Andrieux. Mitochondria as a Cellular Hub in Infection and Inflammation. Int J Mol Sci. 2021; https://doi.org/10.3390/ijms222111338.

  7. Mehta. Association of mitochondria with microtubules inhibits mitochondrial fission by precluding assembly of the fission protein Dnm1. J Biol Chem. 2019; https://doi.org/10.1074/jbc.RA118.006799.

  8. Kühlbrandt. Structure and function of mitochondrial membrane protein complexes. BMC Biol. 2015; https://doi.org/10.1186/s12915-015-0201-x.

  9. Krumova. Overview of Reactive Oxygen Species. Singlet Oxygen Appl Biosci Nanosci. 2016;1 https://doi.org/10.1039/9781782622208-00001.

  10. Rishabh. Radical pairs may explain reactive oxygen species-mediated effects of hypomagnetic field on neurogenesis. PLOS Biol. 2022; https://doi.org/10.1371/journal.pcbi.1010198.

  11. Klotz. Singlet oxygen-induced signaling effects in mammalian cells. Photochem Photobiol Sci. 2003; https://doi.org/10.1039/b210750c.

  12. Hackbarth. Singlet oxygen in vivo: it is all about intensity. J Pers Med. 2022; https://doi.org/10.3390/jpm12060891.

  13. Borden. Dioxygen: what makes this triplet diradical kinetically persistent? J Am Chem Soc. 2017; https://doi.org/10.1021/jacs.7b04232.

  14. Zhang. Fano resonance line shapes in the Raman spectra of tubulin and microtubules reveal quantum effects. Biophys Rep. 2022; https://doi.org/10.1016/j.bpr.2021.100043.

  15. Wang. Human high intelligence is involved in spectral redshift of biophotonic activities in the brain. Biol Sci. 2016a; https://doi.org/10.1073/pnas.1604855113.

  16. Wang X. Quantum dot-like excitonic behavior in individual single walled-carbon nanotubes. Sci Rep. 2016b; https://doi.org/10.1038/srep37167.

  17. Carreá. Tubulin is an inherent component of mitochondrial membranes that interacts with the voltage-dependent anion channel*. J Biol Chem. 2002; https://doi.org/10.1074/jbc.M203834200.

  18. Kelliher. Microtubule control of functional architecture in neurons. Current Opinion in Neurobiology. 2019;(February 07) https://doi.org/10.1016/j.conb.2019.01.003.

  19. Celardo. On the existence of superradiant excitonic states in microtubules. New J Phys. 2019; https://doi.org/10.1088/1367-2630/aaf839.

  20. Collini. Coherently wired light-harvesting in photosynthetic marine algae at ambient temperature. Nature. 2010; https://doi.org/10.1038/nature08811.

  21. Craddock. The feasibility of coherent energy transfer in microtubules. J Royal Soc Interface. 2014; https://doi.org/10.1098/rsif.2014.0677.

  22. Abasto. Exciton diffusion length in complex quantum systems: the effects of disorder and environmental fluctuations on symmetry-enhanced supertransfer. Royal Soc. 2012; https://doi.org/10.1098/rsta.2011.0213.

  23. Rahnama. Emission of mitochondrial biophotons and their effect on electrical activity of membrane via microtubules. J Integr Neurosci. 2011;10(01):65–88. https://doi.org/10.1142/S0219635211002622.

    Article  PubMed  Google Scholar 

  24. Zadeh. Radical pairs may play a role in microtubule reorganization. Sci Rep. 2022; https://doi.org/10.1038/s41598-022-10068-4.

  25. Wilson. Regulation of cytoskeletal dynamics by redox signaling and oxidative stress: implications for neuronal development and trafficking. Front Cell Neurosci. 2015; https://doi.org/10.3389/fncel.2015.00381.

  26. Thar. Propagation of electromagnetic radiation in mitochondria? J Theoretical Biol. 2004; https://doi.org/10.1016/j.jtbi.2004.05.021.

  27. Nganfo. Dynamics of exciton polaron in microtubule. Cell Press J. 2022; https://doi.org/10.1016/j.heliyon.2022.e08897.

  28. Hiramatsu. Self-reduction rate of a microtubule. Int J Modern Phys. 2008; https://doi.org/10.1142/S0129183108012194.

  29. Mammeri. Microtubule-binding core of the tau protein. Sci Adv. 2022; https://doi.org/10.1126/sciadv.abo4459.

  30. Sferra. Microtubule dysfunction: a common feature of neurodegenerative diseases. Int J Mol Sci. 2020; https://doi.org/10.3390/ijms21197354.

  31. Sordillo. The mystery of chemotherapy brain: kynurenines, tubulin and biophoton release. Anticancer Res. 2020; https://doi.org/10.21873/anticanres.14061.

  32. Wijk. Integrating ultra-weak photon emission analysis in mitochondrial research. Front Physiol. 2020; https://doi.org/10.3389/fphys.2020.00717.

  33. Tang. Spatiotemporal imaging of glutamate-induced biophotonic activities and transmission in neural circuits. PLoS One. 2014; https://doi.org/10.1371/journal.pone.0085643.

  34. Singh. Filaments and four ordered structures inside a neuron fire a thousand times faster than the membrane: theory and experiment. J Integr Neurosci. 2021; https://doi.org/10.31083/j.jin2004082.

  35. Liu. Intracellular simulated biophoton stimulation and transsynaptic signal transmission. Appl Phys Lett. 2022; https://doi.org/10.1063/5.0128956.

  36. Omidi. Simulation of nerve fiber based on anti-resonant reflecting optical waveguide. Sci Rep. 2022; https://doi.org/10.1038/s41598-022-23580-4.

  37. Zarkeshian. Photons guided by axons may enable backpropagation-based learning in the brain. Sci Rep. 2022; https://doi.org/10.1038/s41598-022-24871-6.

  38. Kobat. Importance of Müller Cells. Beyoglu Eye J. 2020; https://doi.org/10.14744/bej.2020.28290.

  39. Yang. Cellular signaling in Müller Glia: progenitor cells for regenerative and neuroprotective responses in pharmacological models of retinal degeneration. J Ophthalmol. 2019; https://doi.org/10.1155/2019/5743109.

  40. Tworig. Müller Glia in Retinal Development: From Specification to Circuit Integration. Front Neural Circuits. 2022; https://doi.org/10.3389/fncir.2021.815923.

  41. Lahne. Reprogramming Müller glia to regenerate retinal neurons annual review of vision science. Ann Rev Vision Sci. 2020; https://doi.org/10.1146/annurev-vision-121219-081808.

  42. Campbell. Retinal regeneration requires dynamic Notch signaling. Neural Regenerat Res. 2022; https://doi.org/10.4103/1673-5374.327326.

  43. Franze. Müller cells are living optical fibers in the vertebrate retina. PNAS. 2007; https://doi.org/10.1073/pnas.0611180104.

  44. Marchese. Müller glial cell photosensitivity: a novel function bringing higher complexity to vertebrate retinal physiology. J Photochem Photobiol. 2023; https://doi.org/10.1016/j.jpap.2023.100162.

  45. Bornheim. A dominant vimentin mutant upregulates Hsp70 and the activity of the ubiquitin-proteasome system, and causes posterior cataracts in transgenic mice. J Cell Sci. 2008; https://doi.org/10.1242/jcs.030312.

  46. Zueva. Quantum mechanism of light energy propagation through an avian retina. J Photochem Photobiol B: Biol. 2019; https://doi.org/10.1016/j.jphotobiol.2019.111543.

  47. Khmelinskii. Spectral selectivity model for light transmission by the intermediate filaments in Müller cells. Journal of Photochemistry and Photobiology B: Biology. August. 2017; https://doi.org/10.1016/j.jphotobiol.2017.06.001.

  48. Mano. The pathway of auxin biosynthesis in plants. J Exp Botany. 2012; https://doi.org/10.1093/jxb/ers091.

  49. Alachkar. Aromatic patterns: tryptophan aromaticity as a catalyst for the emergence of life and rise of consciousness. Phys Life Rev. 2022; https://doi.org/10.1016/j.plrev.2022.07.002.

  50. Hameroff. Consciousness, cognition and the neuronal cytoskeleton – a new paradigm needed in neuroscience. Front Mol Neurosci. 2022; https://doi.org/10.3389/fnmol.2022.869935.

  51. Li. Nuclear Spin Attenuates the Anesthetic Potency of Xenon Isotopes in Mice: Implications for the Mechanisms of Anesthesia and Consciousness. Anesthesiology. 2018;

    Google Scholar 

  52. Hameroff. ‘Orch OR’ is the most complete, and most easily falsifiable theory of consciousness. Cognit Neurosci. 2020; https://doi.org/10.1080/17588928.2020.1839037.

  53. Fröhlich. The extraordinary dielectric properties of biological materials and the action of enzymes. PNAS. 1975;72(11):4211–5.

    Article  PubMed  PubMed Central  Google Scholar 

  54. Fisher. Quantum cognition: The possibility of processing with nuclear spins in the brain. Ann Phys. 2015; https://doi.org/10.1016/j.aop.2015.08.020.

  55. Lindström. Consciousness as the collective excitation of a brainwide web – understanding consciousness from below quantum fields to above neuronal networks. J Phys Conference Series. 2018; https://doi.org/10.1088/1742-6596/1275/1/012021.

  56. Tuszynski. From quantum chemistry to quantum biology: a path toward consciousness. J Integr Neurosci. 2020; https://doi.org/10.31083/j.jin.2020.04.393.

  57. Kronemer. Human visual consciousness involves large scale cortical and subcortical networks independent of task report and eye movement activity. Nature. 2022; https://doi.org/10.1038/s41467-022-35117-4.

  58. Blumenfeld. Brain mechanisms of conscious awareness: detect, pulse, switch, and wave. Neuroscientist. 2021; https://doi.org/10.1177/10738584211049378.

  59. Shan. Mapping the emergence of visual consciousness in the human brain via brain-wide intracranial electrophysiology. Innovation. 2022; https://doi.org/10.1016/j.xinn.2022.100243.

  60. DiGregorio. Tuning alpha rhythms to shape conscious visual perception. Curr Biol. 2022; https://doi.org/10.1016/j.cub.2022.01.003.

  61. Fakche. α phase-amplitude tradeoffs predict visual perception. eNeuro. 2022; https://doi.org/10.1523/ENEURO.0244-21.2022.

  62. Aerts. Human perception as a phenomenon of quantization. Entropy. 2022; https://doi.org/10.3390/e24091207.

  63. Ocklenburg. Symmetry and asymmetry in biological structures. PNAS. 2022; https://doi.org/10.1073/pnas.2204881119.

  64. Dyakin. Fundamental cause of bio-chirality: space-time symmetry—concept review. Symmetry. 2022; https://doi.org/10.3390/sym15010079.

  65. Glattfelder. The Unification Power of Symmetry. Front Collect. 2019; https://doi.org/10.1007/978-3-030-03633-1_4.

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

Copyright information

© 2023 The Author(s), under exclusive license to Springer Nature Switzerland AG

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Moazed, K.T. (2023). The Quantum Biology of Consciousness and Visual Perception. In: Quantum Biology of the Eye . Springer, Cham. https://doi.org/10.1007/978-3-031-32060-6_7

Download citation

  • DOI: https://doi.org/10.1007/978-3-031-32060-6_7

  • Published:

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-031-32059-0

  • Online ISBN: 978-3-031-32060-6

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics