The human retina consists of two types of photoreceptor cells: cone cells and rod cells.
Rod cells are evenly distributed around the periphery of the retina but are not located in the central fovea.
Cone cells are mainly located in the central fovea of the retina.
There are no photoreceptors at the blind spot where ganglion axon fibres form the optic nerve.
Rod cells do not generate action potentials in the dark due to the following process: Na+ enters the outer segment of the rod cell via non-specific cation channels.
Active transport of Na+ out of the inner segment of the rod cell slightly depolarises the cell.
When a certain threshold of depolarisation is reached, voltage-gated Ca2+ channels open, triggering the exocytosis of glutamate.
Glutamate acts as an inhibitory neurotransmitter to hyperpolarise a bipolar neuron.
Rod cell becomes hyperpolarised.
Rod cells are very sensitive due to spatial summation of subthreshold impulses, which allows them to see in low-light conditions.
Bipolar neuron depolarises.
Rod cells generate an action potential in the light.
Cone cells contain three types of iodopsin which absorb red, blue or green wavelengths of light, giving them tricolour vision.
No glutamate is released, so no inhibitory signal.
Cone cells have 1 cone cell synapse with 1 bipolar neuron, which results in no retinal convergence and high resolution.
Rod cells have many rod cells synapse with 1 bipolar neuron, which results in low resolution.
Cone cells are less sensitive, which affects their vision in bright light.
Opsin closes cation channels via a hydrolysis reaction.
Rhodopsin absorbs all wavelengths of light, which gives rod cells monochromatic vision.
Rhodopsin pigment bleaches when it absorbs light and breaks down into opsin and retinal.
Active transport of Na+ out of the inner segment continues.