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4-25-05
Vision and other sensors
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Figure 49.11 Photoreceptors in the vertebrate retina
Direction of Light
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• Photoreceptors of the retina (humans).
– About 125 million rod cells.• Rod cells are light sensitive but do not distinguish colors.
– About 6 million cone cells.150,000 / sq mm while hawks have a million / sq mm. There for can spot rodents when high in the sky.• Not as light sensitive as rods but provide color vision.
• Most highly concentrated on the fovea – an area of the retina that lacks rods.
• Human cone opsins absorb in red, blue and green. Three types Some animals have opsins that absorb in ultraviolet region and deep water fish lack red opsin cuz no red light.
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Figure 49.12 Effect of light on retinal
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The light-absorbing pigment rhodopsin triggers a signal-transduction pathway. Sodium channel is open
neurotransmiter being released.
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• Rhodopsin (retinal + opsin) is the visual pigment of rods.
• The absorption of light by rhodopsin initiates a signal-transduction pathway.
Fig. 49.13
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Figure 49.14 The effect of light on synapses between rod cells and bipolar cells
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• Color reception is more complex than the rhodopsin mechanism.
– There are three subclasses of cone cells each with its own type of photopsin.• Color perception is based on the brain’s analysis
of the relative responses of each type of cone.
– In humans, colorblindness is due to a deficiency, or absence, of one or more photopsins.• Inherited as an X-linked trait.
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The retina assists the cerebral cortex in processing visual information
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• Visual processing begins with rods and cones synapsing with bipolar cells.
– Bipolar cells synapse with ganglion cells.
• Visual processing in the retina also involves horizontal cells and amacrine cells.
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Fig. 49.15
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• Vertical pathway: photoreceptors bipolar cells ganglion cells axons.
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• Lateral pathways:
– Photoreceptors horizontal cells other photoreceptors.• Results in lateral inhibition.
– More distance photoreceptors and bipolar cells are inhibited sharpens edges and enhances contrast in the image.
– Photoreceptors bipolar cells amacrine cells ganglion cells.• Also results in lateral inhibition, this time of the
ganglion cells.
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• The optic nerves of the two eyes meet at the optic chiasm.– Where the nasal half of each
tract crosses to the opposite side.
• Ganglion cell axons make up the optic tract.– Most synapse in the
lateral geniculate nuclei of the thalamus.• Neurons then convey
information to the primary visual cortex of the optic lobe.
Fig. 49.16
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Hearing And Equilibrium
1. The mammalian hearing organ is within the ear
2. The inner ear also contains the organs of equilibrium
3. A lateral line system and inner ear detect pressure waves in most fishes and
aquatic amphibians
4. Many invertebrates have gravity sensors and are sound-sensitive
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• The outer ear includes the external pinna and the auditory canal.
– Collects sound waves and channels them to the tympanic membrane.
The mammalian hearing organ is within the ear
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Fig. 49.17
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• From the tympanic membrane sound waves are transmitted through the middle ear.
– Malleus incus stapes.
– From the stapes the sound wave is transmitted to the oval window and on to the inner ear.
– Eustachian tube connects the middle ear with the pharynx.
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• The inner ear consists of a labyrinth of channels housed within the temporal bone.
– The cochlea is the part of the inner ear concerned with hearing.• Structurally it consists of the upper vestibular canal
and the lower tympanic canal, which are separated by the cochlear duct.
• The vestibular and tympanic canals are filled with perilymph.
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– The cochlear duct is filled with endolymph.
– The organ of Corti rests on the basilar membrane.• The tectorial membrane rests atop the hair cells of
the organ of Corti.
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• From inner ear structure to a sensory impulse: follow the vibrations.
– The round window functions to dissipate the vibrations.
• Vibrations in the cochlear fluid basilar membrane vibrates hair cells brush against the tectorial membrane generation of an action potential in a sensory neuron.
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Fig. 49.18
Basilar membrane sensitiveto frequency
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Fig. 49.17
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• Pitch is based on the location of the hair cells that depolarize.
• Volume is determined by the amplitude of the sound wave.
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• Behind the oval window is a vestibule that contains the utricle and saccule.
– The utricle opens into three semicircular canals.
The inner ear also contains the organs of equilibrium
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Fig. 49.19
Otoliths ear stones/bones
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• The utricle and saccule respond to changes in head position relative to gravity and movement in one direction.
– Hair cells are projected into a gelatinous material containing otoliths.• When the head’s orientation changes the hair cells
are tugged on nerve impulse along a sensory neuron.
• The semicircular canals respond to rotational movements of the head.
– The mechanism is similar to that associated with the utricle and saccule.
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• Fishes and amphibians lack cochleae, eardrums, and openings to the outside.– However, they have saccules, utricles, and
semicircular canals.(Fish have large ear bones that increase in size as the fish grows. Lay down alternating layers (annuli) of protein and calcium carbonate. Can age fish by counting the rings (annuli) because they are spaced further apart during the summer when growth is maximum.
A lateral line system and inner ear detect pressure waves in most fishes
and aquatic amphibians
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• Most fish and amphibians have a lateral line system along both sides of their body.– Contains
mechanoreceptors that function similarly to mammalian inner ear.
– Provides a fish with information concerning its movement through water or the direction and velocity of water flowing over its body.
Copyright © 2002 Pearson Education, Inc., publishing as Benjamin CummingsFig. 49.20
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• Statocysts are mechanoreceptors that function in an invertebrates sense of equilibrium.
– Statocysts function is similar to that of the mammalian utricle and saccule.
Many invertebrates have gravity sensors and are sound-sensitive
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Fig. 49.21
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• Sound sensitivity in insects depends on body hairs that vibrate in response to sound waves.– Different hairs respond to different frequencies.
• Many insects have a tympanic membrane stretched over a hollow chamber.
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Fig. 49.22
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Chemoreception – Taste And Smell
1. Perceptions of taste and smell are usually interrelated
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• Taste receptors in insects are located on their feet.
Insect taste receptors
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Fig. 49.23Colors represent different
Types of receptors
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• In mammals, taste receptors are located in taste buds most of which are on the surface of the tongue.( recognize 4 basic tastes: sweet, sour, bitter and salty).
• Each taste receptor responds to a wide array of chemicals.– It is the pattern of taste receptor response that
determines something’s perceived flavor (description of a “good” wine). What are they tasting???
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• In mammals, olfactory receptors line the upper portion of the nasal cavity.– The binding of odor molecules to olfactory receptors
initiate signal transduction pathways involving a G-protein-signaling pathway and, often, adenylyl cyclase and cyclic AMP.
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Fig. 49.24
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• Although taste and olfaction use separate pathways to separate centers they are interrelated. We can’t taste food very well if we have a head cold and olfactory epithelium is non-functional.
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MOTOR SYSTEMS
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Movement And Locomotion
1. Locomotion requires energy to overcome friction and gravity
2. Skeletons support and protect the animal body and are essential to movement
3. Physical support on land depends on adaptations of body proportions and posture
4. Muscles move skeletal parts by contracting
5. Interactions between myosin and actin generate force during muscle contractions
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• A comparison of the energy costs of various modes of locomotion.
Locomotion requires energy to overcome friction and gravity
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Fig. 49.25 Swimming less energy
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• Swimming.
– Since water is buoyant gravity is less of a problem when swimming than for other modes of locomotion.• However, since water is dense, friction is more of a
problem.– Fast swimmers have fusiform bodies.
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• For locomotion on land powerful muscles and skeletal support are more important than a streamlined shape. (Kangaroo not a particularly graceful animal).– When hopping the tendons in kangaroos legs store
and release energy like a spring that is compressed and released – the tail helps in the maintenance of balance.
– When walking having one foot on the ground helps in the maintenance of balance.
– When running momentum helps in the maintenance of balance.
– Crawling requires a considerable expenditure of energy to overcome friction – but maintaining balance is not a problem.
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• Gravity poses a major problem when flying.– The key to flight is the aerodynamic structure of
wings.
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Fig. 34.26 Reduction of skeletal weight and organs
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• Cellular and Skeletal Underpinning of Locomotion.
– On a cellular level all movement is based on contraction.• Either the contraction of microtubules or the
contraction of microfilaments.
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• Hydrostatic skeleton: consists of fluid held under pressure in a closed body compartment.– Form and movement is controlled by changing the
shape of this compartment.– The hydrostatic skeleton of earthworms allow them to
move by peristalsis.– Advantageous in aquatic environments and can
support crawling and burrowing.– Do not allow for running or walking.
Skeletons support and protect the animal body and are essential to
movement
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• Exoskeletons: hard encasements deposited on the surface of an animal.– Mollusks are enclosed in a calcareous
exoskeleton.
– The jointed exoskeleton of arthropods is composed of a cuticle.• Regions of the cuticle can vary in hardness and degree of
flexibility.• About 30 – 50% of the cuticle consists of chitin.• Muscles are attached to the interior surface of the cuticle.• This type of exoskeleton must be molted to allow for
growth.
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• Endoskeletons: consist of hard supporting elements within soft tissues.
– Sponges have spicules.
– Echinoderms have plates composed of magnesium carbonate and calcium carbonate.
– Chordate endoskeletons are composed of cartilage and bone.• The bones of the mammalian skeleton are
connected at joints by ligaments.
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Fig. 49.28
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• Muscles come in antagonistic pairs.
Muscles move skeletal parts by contracting
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Fig. 49.30
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• Structure and Function of Vertebrate Skeletal Muscle.– The sarcomere is the
functional unit of muscle contraction.
– Thin filaments consist of two strands of actin and one tropomyosin coiled about each other.
– Thick filaments consist of myosin molecules.
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Fig. 49.31
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The sliding-filament model of muscle contraction.
Interactions between myosin and actin generate force during muscle
contractions
Copyright © 2002 Pearson Education, Inc., publishing as Benjamin CummingsFig. 49.33
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• At rest tropomyosin blocks the myosin binding sites on actin.
• When calcium binds to the troponin complex a conformational change results in the movement of the tropomyosin-tropinin complex and exposure of actin’s myosin binding sites.
Calcium ions and regulatory proteins control muscle contraction
Copyright © 2002 Pearson Education, Inc., publishing as Benjamin CummingsFig. 49.34
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• But, wherefore the calcium ions?
– Follow the action potential.
– When an action potential meets the muscle cell’s sarcoplasmic reticulum (SR) stored Ca2+ is released.
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Fig. 49.35
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• Review of skeletal muscle contraction.
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Fig. 49.36
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• An individual muscle cell either contracts completely or not all.
• Individual muscles, composed of many individual muscle fibers, can contract to varying degrees.– One way variation is
accomplished by varying the frequency of action potentials reaching the muscle from a single motor neuron.
Diverse body movements require variation in muscle activity
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Fig. 49.37
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– Graded muscle contraction can also be controlled by regulating the number of motor units involved in the contraction.
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Fig. 49.38
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– Recruitment of motor neurons increases the number of muscle cells involved in a contraction.
– Some muscles, such as those involved in posture, are always at least partially contracted.• Fatigue is avoided by rotating among motor units.
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