Photosynthesis is all about light and how light organizes our tissues from embryo to adult form. Nocturnal mammals and daytime animals have eyes that are different. Since you all now know that the eyes/skin control all growth and metabolism do you realize what it means for modern nutritional and biochemical data? We need to augment the human battery with good choices that uses photosynthetic pathways because glass subtracts out all UV and 30-50% of the IR-A. This makes everyone inside blue light toxic by design. Today the lighting in virtually all research laboratories is still the responsibility of the janitor and is classified as ordinary building maintenance instead of being part of the experimental design. This is why the research in nutrition and biochemistry is worthless, in my opinion. When you add in the fact that they usually study mice and rats who are nocturnal they completely miss all the good data because humans have photopic eyes and skin. Why? Your human photopic eyes mean your biology is not designed around the scotopic eating of food or light. The simple quantum rule says Mother Nature's mitochondrial design. Mice and rats retinae are scotopic. Because IR-A, B, and C light provide a molecular boost to the mitochondria not previously recognized until June of 2018. Infrared spectrum gives cytochrome c oxidase a ‘molecular kick’ to the mitochondria from the 42% of red light in the sun’s rays that are present from sunrise to sunset that goes from 600nm-3100nm light; this informs or tells (information quanta) the cell to turn on a large number of antioxidant and energy-boosting genes only when ATP is being made by the combination of IRA and UV light we see in parts of a day. Water viscosity changes with the red light in sunlight to facilitate the ATPase to work at 100% photothermal efficiency. That boost is greater when UVA and/or UVB light are present because of both of those UV frequencies BOTH slow ECT at different places on the inner mitochondrial membrane from cytochrome 1-4 by a quantum stimulus/design. Cytochrome c oxidase has 4 red windows at 620, 680, 760, and 820nm of light. Those are some frequencies to consider. Hemoglobin has a sharp cut off at 600 nm. This leaves a lot of red frequency the sun provides to animals on Earth above 820nm light. It now turns out that light can be used photosynthetically too in ways we are learning. Both are heme proteins which act as circadian time crystals with radically different optical windows. Cytochrome c oxidase is present in mitochondria and RBC have a ton of hemoglobin in their cells which is HAVE NO mitochondria by design because of these light mechanisms. RBC’s are designed to ferry 280-600 nm (IRA and UVA light) 600nm-1000nm red light would cover the activation of fibroblasts to make collagen to stimulate repairs mechanisms. This means humans have a deep ability to go behind the red region to make energy from light that will re-write the biology. It means what happened at ocean vents explains why life began where IR B and C are found and that means the assumptions of guys like Nick Lane have left a lot of fat on the bone with respect to LUCA and where and how mitochondria can operate even today. This means just being outside is photosynthetic for any animal with mitochondria. This is why outdoor life is required for animals and is NOT A SUGGESTION. This is why clothing and make up present new problems for modern humans to consider. Presently, no one believes that any plant or marine life uses anything but 400-780 nm, which is the photosynthetic optical window of plants that form the entire food web on Earth. I've known that was bullshit for years because cytochrome c goes above where photosynthesis chlorophyll A and B operate. Now we know for sure today's the books are wrong on what they've taught about photosynthesis. When you know better you do better. Black Swans do. IT IS TIME to join my tribe now. ncbi.nlm.nih.gov/pmc/articles/P…
