The ability to detect scents comes from olfactory receptor (OR) proteins found in the sensory neurons inside the nose.
Each OR protein binds to a specific type of odor molecule, sending signals to the brain.
The diversity of OR proteins allows animals to distinguish thousands of different smells.
Humans have about 1,000 olfactory receptor genes, but nearly half are nonfunctional (pseudogenes)—they no longer produce working proteins.
In contrast, mammals like dogs and mice have most of their olfactory genes still functional, giving them a far superior sense of smell.
This suggests that humans have lost some reliance on smell over evolutionary time.
Fish: They have olfactory genes that detect chemicals in water, but their receptors are different from land animals because water carries scents differently than air.
Amphibians & Reptiles: Many have Jacobson’s organ (vomeronasal organ, VNO), which detects pheromones—chemicals used for communication. Snakes famously use it when flicking their tongues.
Mammals: Many have both olfactory receptors and a functional VNO, but primates (including humans) have a reduced or nonfunctional VNO.
Humans: As primates evolved better vision, their need for an acute sense of smell declined, leading to the loss of many olfactory genes.
The shared structure of olfactory genes across species shows that the ability to detect odors evolved long before mammals or land animals appeared.
Mutations and gene loss in primates indicate natural selection favors vision over smell in certain environments.
The fact that humans still carry pseudogenes for smell reveals our evolutionary history—we have the genetic remnants of a highly sensitive olfactory system that was once essential.
Light enters the eye, passing through the cornea and lens, which focus it onto the retina at the back of the eye.
The retina contains photoreceptor cells:
Rods: Detect low light, black-and-white vision.
Cones: Detect color, require bright light.
The optic nerve transmits signals from these cells to the brain.
The simplest form of light detection appears in single-celled organisms, which have light-sensitive proteins but no actual eyes.
Flatworms have eye spots—clusters of light-sensitive cells that allow them to sense the direction of light.
Mollusks (e.g., squid and octopuses) developed camera-like eyes, independently from vertebrates.
Vertebrates' eyes evolved from a patch of light-sensitive cells that folded inward, forming a primitive lens and retina.
A single gene, Pax6, controls eye development across species.
When scientists inserted mouse Pax6 genes into fruit flies, the flies still developed normal fly eyes—not mouse eyes—suggesting that Pax6 is a universal eye-building gene.
This discovery showed that the genetic blueprint for eyes is ancient, dating back to a common ancestor of insects, mollusks, and vertebrates.
The vertebrate retina is wired backward—light must pass through layers of nerve cells before reaching the photoreceptors.
This design creates a blind spot, which is absent in octopuses, whose eyes are better structured.
This shows that eyes were not perfectly designed but rather shaped by evolutionary constraints.
Most mammals see in two colors (dichromatic vision), but primates evolved a third type of cone, allowing for trichromatic vision (red, green, and blue).
This adaptation was likely driven by the need to spot ripe fruit in trees.
Eyes evolved multiple times independently, but they all share a common genetic foundation.
Despite their complexity, eyes were not built from scratch but modified from simpler structures over millions of years.
Sound waves are funneled into the outer ear, causing the eardrum to vibrate.
The vibrations pass through three tiny bones (ossicles) in the middle ear:
Malleus (hammer)
Incus (anvil)
Stapes (stirrup)
The ossicles amplify the sound and transmit it to the cochlea, a fluid-filled structure in the inner ear that converts vibrations into nerve signals.
Fish do not have eardrums or middle ear bones, but they detect vibrations in water through their lateral line system.
Early land animals evolved a single middle ear bone (stapes) to amplify airborne sound.
Reptiles and early mammals developed additional bones to improve hearing.
In mammals, two jawbones from reptilian ancestors shrank and moved into the middle ear, forming the three-bone system unique to mammals.
Tiktaalik (375 million years ago) had a skull structure that suggests an early form of sound detection on land.
Therapsids (mammal-like reptiles) had intermediate stages of jawbones evolving into ear bones.
Fossils show how the reptilian jaw joint (articular and quadrate bones) transitioned into the mammalian ear ossicles (malleus and incus).
The transformation of jawbones into ear bones is one of the best-documented examples of how structures can change function over time.
The connection between our jaw and ear still exists in embryos—human fetuses briefly have jawbones that resemble those of reptiles before shifting into ear bones.
Our bodies are built from ancient structures, from fish-like embryos to reptilian jawbones.
Evolution explains why our bodies have flaws—we are not perfectly designed but shaped by history.
Birth defects can be explained by developmental genes inherited from ancestors.
Back pain and hernias result from our shift to bipedalism, which put stress on a skeleton originally adapted for walking on all fours.
Tinnitus (ringing in the ears) is likely an evolutionary leftover from early sound detection systems.
Evolution is not just about fossils—it has real implications for human health, biology, and medicine.
By understanding our evolutionary past, we can better understand and address issues in the present.