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External Structure and locomotion
All animals have external structures, or bodily organs on the outside. The majority of animals
have a head, a body covering, limbs, and a tail of some kind. These body parts are all
essential to an animal's ability to live and reproduce, despite the fact that they may appear
differently on different animals.
The limbs of mammals may be modified for a particular movement. They could be taught
how to swim, fly, climb, and run. More commonly known as "ricochetal locomotion," saltatory
(leaping) movement has been observed in a variety of unrelated species (some marsupials,
lagomorphs, and several independent lineages of rodents).
Skin
The skin of mammals, like that of other vertebrates, consists of epidermal and dermal
layers. It protects against actual injury, microbiological invasion, and UV rays from the sun.
skin is also important for temperature regulation, sensory perception excretion, and water
regulation.
Hair
Hairs are a keratinized derivative of the epidermis of the skin and are uniquely mammalian.
It is seated in an invagination of the epidermis called a hair follicle. Two distinct kinds of hair
typically compose a pelage, a coat of hair. Long guard hairs protect a dense coat of shorter,
insulating under hairs.
Hair must periodically molt because it is made mainly of dead cells. In some mammals (e.g.,
humans), molting occurs gradually and may not be noticed. Others have rapid hair loss,
which could alter the characteristics of their pelage. In the fall, many mammals acquire a
thick coat of insulting under hair, and the pelage color may change.
For example, the Arctic fox takes on a white or cream color with its autumn molt, which helps
conceal the fox in a snowy environment. with its spring molt, the Arctic fox acquires a gray
and yellow pelage (see figure 2).
(Figure 2) Arctic fox
Hairs are also important for the sense of touch. The mechanical displacement of hair
stimulates nerve cells associated with the hair root. Guard hairs may sometimes be modified
into thick-shifted hairs called vibrissae. Vibrissae occur around the legs, nose, mouth, and
eyes of very sensitive to displacement.
Air space in the hair shaft and hair trapped between hairs and the skin provides an effective
insulating layer. A band of smooth muscle, called the arrector pili muscle, runs between the
hair follicle and lower epidermis. when the muscle contract, the hair stands upright,
increasing the amount of air trapped the in the pelage and improving its insulating properties.
Arrector pili muscles are under the control of the autonomic nervous system, which also
controls a mammal's "fight-or-flight" response. In threatening situations, the hair stands on
end and may give the perception of increased size and strength.
● Circulation, Gas Exchange and Temperature Regulation in Mammals
● Excretion and Osmoregulation In Mammals
● Reproduction and Development in Mammals
Hair color depend on the number of pigments (melanin) deposited in it and the quantity of
air in the hair shaft. The pelage of most mammals is dark above and lighter underneath. This
pattern them less conspicuous under most conditions. Some mammals advertised their
defenses using aposematic (warning) coloration. The contrasting marking of a skunk is a
familiar example.
Pelage is reduced in large mammals from hot climates (such as those seen in elephants and
hippopotamuses) and some aquatic mammals (e.g. Whales) that often have fatty insulation.
A few mammals (e.g. naked mole rats) have almost no pelage (see figure 3).
Claws
Claws are present in all amniote classes. For locomotion, as well as for offensive and
defensive behaviors. Claws form from accumulations of keratin that cover the terminal
phalanx (bone) of the digits. Some mammals, they are specialized to form nails or hooves
(see figure 4).
Glands develop from the epidermis of the skin. Sebaceous (oil) glands are associated with
hair follicles, and their oily secretion lubricates and waterproofs the skin and hair. most
mammals also possess sudoriferous (sweat) glands.
Small sudoriferous glands (eccrine glands) release watery secretions used in evaporative
cooling. Large sudoriferous glands (apocrine glands) secrete a mixture of salt, urea, and
water, which microorganisms on the skin convert to odorous products.
Scent or musk glands
Scent or musk glands are around the face, feet, or anus of many mammals. These glands
secrete pheromones, which may be involved with defense, species ad sex recognition, and
territorial behavior.
Mammary gland
Mammary glands are functional in female mammals and are present, but non-functional, in
males. The milk that mammary glands secrete contains water, carbohydrates (especially the
sugar lactose), fats, protein, minerals, and antibodies. Mammary glands are probably
derived evolutionarily from apocrine glands and usually contain substantial fatty deposits.
Monotremes have mammary glands that lack nipples. The glands discharge milk into
depressions on the belly, where the young lap it up. In other mammals, mammary glands
open via nipples or teats, and the young suckle for their nourishment (see figure 5).
The Skull and Teeth
The skull of mammals shows important modifications of the reptilian pattern. One feature
that zoologists used to distinguish reptilian from mammal skulls is the methods of jaw
articulation. In reptiles, the jaws articulate at two small bones at the rear of the jaw. In
mammals, these bones have moves into the middle ear, and along with the stapes, form the
middle ear ossicles. A single bone of the lower jaw articulates the mammalian jaw.
A secondary palate evolved twice in vertebrates in the archosaur lineage and in the
synapsid lineage. In some therapsids, small, shelf-like extensions of bones (the hard palate)
partially separated the nasal and oral passageways. The soft palate, a posterior extension
of the secondary palate in animals, separates the mouth cavity from the nasal passages
almost completely.
Some mammals chew their food before ingesting it, like other vertebrates that do. The more
extensive secondary palate allows mammals to breathe while chewing, Breathing needs to
stop only briefly during swallowing (see figure 6).
Teeth's arrangement and form are important indicators of mammalian lifestyle. In reptiles, the
teeth are uniformly conical, a condition referred to as homodont. In mammals, the teeth are
open and specialized for different functions, a condition called heterodont. Recall that in
reptiles other than archosaurs, teeth were acrodont and attached along the top or inside of
the jaw.
In mammals ( as well as crocodylians) teeth is thecodont. That is, teeth are set into sockets
of the jaw. For most of their lives, mammals have two sets of teeth. Deciduous or milk
teeth, which appear before or soon after birth, are the first teeth. Permanent teeth come in to
replace these missing pieces. The term "diphyodont condition" relates to this single tooth
replacement.
Adult mammals have up to four kinds of teeth.
1. Incisors
Incisors are the most anterior teeth in the jaws. They are usually chisel-like and used for
gnawing or nipping.
2. Canine
Canine are often long, stour, and conical. They are usually for catching, killing, and tearing
prey. The Canine and incisor have single roots.
3. Premolars
Premolars are positioned next to the canine and have one or two roots and truncated
surfaces for chewing.
4. Molars
Molars have broad chewing surfaces and two (upper molars) or three (lower molars) roots.
Mammalian species have a characteristic number of each kind of adult tooth. Zoologists use
a dental formula to characterize taxa It is an expression of the number of teeth of each kind
in one-half of the upper and lower jaws. The teeth of the upper jaws are listed below those of
the lower jaws and in the following order: Incisors, Canine, Premolar, and Molars. For
example:
Human Beaver
2 ∙ 1 ∙ 2 ∙
3
1 ∙ 0 ∙ 1 ∙ 3
2 ∙ 1 ∙ 2 ∙
3
1 ∙ 0 ∙ 1 ∙ 3
Mammalian teeth (dentition) may be specialized for a particular diet. In some mammals, the
dentition is reduced, sometimes to the point of having no teeth, For example, armadillos and
the giant anteater (order Edentata) feed on termites and ants, and their teeth are reduced.
Some mammals (e.g. humans, order primates; and pigs, order Artiodactyla) are omnivorous;
they feed on a variety of plants and animal materials. They have teeth with flat grinding
surfaces for rupturing plant cell walls in the back and teeth with sharp ripping and piercing
surfaces in the front (see figure 7).
Mammals that eat plant material often have flat, grinding posterior teeth and incisors, and
sometimes have canines modified for nipping plant matter (e.g. horses, order
Perissodactyla; deer, order Artiodactyla) or gnawing (e.g. rabbits, order Lagomorpha;
beavers, order Rodentia) (figure 4b and c). In rodents, the incisor grows throughout life.
Although most mammals have enamel covering the entire tooth, rodents have enamel only
on the front of their incisors.
The teeth are kept sharp by slower wear in front than in the back. A gap called the diastema
separates the interior food-procuring teeth from the posterior grinding teeth. The diastema
results from an elongation of the snout that allows the interior teeth to reach close to the
ground or into narrow openings to procure food.
The posterior teeth have a high, exposed surface (crown) and continuous growth, which
allow these teeth to withstand years of grinding tough vegetation.
Canines and incisors are used by predatory mammals to catch, kill, and tear prey. In
members of the order Carnivora (e.g. coyotes, dogs, and cats), the fourth upper premolars
and first lower molars form a scissor-like shearing surface, called the carnassial apparatus,
that is used for cutting flesh from prey (figure 4d).
The Vertebral Column
The Vertebral column of mammals is divided into five regions. As with reptiles and birds, the
first two cervical vertebrae are the atlas and axis. Five other cervical vertebrae usually follow.
Even the giraffe and Whale have seven neck vertebrae, which are greatly elongated or
compressed, respectively. In contrast, tree sloths have either six or nine cervical vertebrae,
and the manatee has six cervical vertebrae.
The trunk is divided into thoracic and lumber regions, as is the case for birds. In Mammals,
the division is correlated with their methods of breathing. The thoracic region contains the
ribs. Most ribs connect to the thoracic vertebrae and to the sternum via costal cartilages.
Other ribs are attached only to the thoracic vertebrae or to the other ribs through cartilages.
All ribs protect the heart and lungs. The articulation between the thoracic vertebrae provides
the flexibility needed in turning, climbing, and lying on the side to suckle young. Lumber
vertebrae have interlocking processes that give support, but little freedom of movement.
Appendicular skeleton
The appendicular skeleton of mammals rotates under the body so that the appendages are
usually directly beneath the body. Joints usually limit the movement of appendages to the
single anteroposterior plan, causing the tips of the appendages to move in long arcs.
The bones of the pelvic girdle are fused in the adult, a condition that is advantageous for
locomotion but presents problems during the birth of offspring. In a pregnant female, the
ventral joint between the halves of the pelvis the public symphysis loosens before birth,
allowing the pelvis to spread during birth.
Muscles
Most mammals, they generated the weight of the body because the appendages are located
directly beneath the body. Upper appendages and girdles contain most of the body's muscle
mass. Manny running mammals (e.g. deer order Artiodactyla) have little muscle in their
lower leg that would slow leg movement. Instead, tendons run from muscles high in the leg
to cause movement at the lower joints.
● Human respiratory system
● Endocrine System of Mammals
● The Heart and Circulatory system of Mammals

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External Structure and locomotion.pdf

  • 1. External Structure and locomotion All animals have external structures, or bodily organs on the outside. The majority of animals have a head, a body covering, limbs, and a tail of some kind. These body parts are all essential to an animal's ability to live and reproduce, despite the fact that they may appear differently on different animals. The limbs of mammals may be modified for a particular movement. They could be taught how to swim, fly, climb, and run. More commonly known as "ricochetal locomotion," saltatory (leaping) movement has been observed in a variety of unrelated species (some marsupials, lagomorphs, and several independent lineages of rodents). Skin The skin of mammals, like that of other vertebrates, consists of epidermal and dermal layers. It protects against actual injury, microbiological invasion, and UV rays from the sun. skin is also important for temperature regulation, sensory perception excretion, and water regulation.
  • 2. Hair Hairs are a keratinized derivative of the epidermis of the skin and are uniquely mammalian. It is seated in an invagination of the epidermis called a hair follicle. Two distinct kinds of hair typically compose a pelage, a coat of hair. Long guard hairs protect a dense coat of shorter, insulating under hairs. Hair must periodically molt because it is made mainly of dead cells. In some mammals (e.g., humans), molting occurs gradually and may not be noticed. Others have rapid hair loss, which could alter the characteristics of their pelage. In the fall, many mammals acquire a thick coat of insulting under hair, and the pelage color may change. For example, the Arctic fox takes on a white or cream color with its autumn molt, which helps conceal the fox in a snowy environment. with its spring molt, the Arctic fox acquires a gray and yellow pelage (see figure 2). (Figure 2) Arctic fox Hairs are also important for the sense of touch. The mechanical displacement of hair stimulates nerve cells associated with the hair root. Guard hairs may sometimes be modified into thick-shifted hairs called vibrissae. Vibrissae occur around the legs, nose, mouth, and eyes of very sensitive to displacement. Air space in the hair shaft and hair trapped between hairs and the skin provides an effective insulating layer. A band of smooth muscle, called the arrector pili muscle, runs between the hair follicle and lower epidermis. when the muscle contract, the hair stands upright, increasing the amount of air trapped the in the pelage and improving its insulating properties. Arrector pili muscles are under the control of the autonomic nervous system, which also controls a mammal's "fight-or-flight" response. In threatening situations, the hair stands on end and may give the perception of increased size and strength. ● Circulation, Gas Exchange and Temperature Regulation in Mammals ● Excretion and Osmoregulation In Mammals ● Reproduction and Development in Mammals
  • 3. Hair color depend on the number of pigments (melanin) deposited in it and the quantity of air in the hair shaft. The pelage of most mammals is dark above and lighter underneath. This pattern them less conspicuous under most conditions. Some mammals advertised their defenses using aposematic (warning) coloration. The contrasting marking of a skunk is a familiar example. Pelage is reduced in large mammals from hot climates (such as those seen in elephants and hippopotamuses) and some aquatic mammals (e.g. Whales) that often have fatty insulation. A few mammals (e.g. naked mole rats) have almost no pelage (see figure 3). Claws Claws are present in all amniote classes. For locomotion, as well as for offensive and defensive behaviors. Claws form from accumulations of keratin that cover the terminal phalanx (bone) of the digits. Some mammals, they are specialized to form nails or hooves (see figure 4).
  • 4. Glands develop from the epidermis of the skin. Sebaceous (oil) glands are associated with hair follicles, and their oily secretion lubricates and waterproofs the skin and hair. most mammals also possess sudoriferous (sweat) glands. Small sudoriferous glands (eccrine glands) release watery secretions used in evaporative cooling. Large sudoriferous glands (apocrine glands) secrete a mixture of salt, urea, and water, which microorganisms on the skin convert to odorous products. Scent or musk glands Scent or musk glands are around the face, feet, or anus of many mammals. These glands secrete pheromones, which may be involved with defense, species ad sex recognition, and territorial behavior. Mammary gland Mammary glands are functional in female mammals and are present, but non-functional, in males. The milk that mammary glands secrete contains water, carbohydrates (especially the sugar lactose), fats, protein, minerals, and antibodies. Mammary glands are probably derived evolutionarily from apocrine glands and usually contain substantial fatty deposits.
  • 5. Monotremes have mammary glands that lack nipples. The glands discharge milk into depressions on the belly, where the young lap it up. In other mammals, mammary glands open via nipples or teats, and the young suckle for their nourishment (see figure 5). The Skull and Teeth The skull of mammals shows important modifications of the reptilian pattern. One feature that zoologists used to distinguish reptilian from mammal skulls is the methods of jaw articulation. In reptiles, the jaws articulate at two small bones at the rear of the jaw. In mammals, these bones have moves into the middle ear, and along with the stapes, form the middle ear ossicles. A single bone of the lower jaw articulates the mammalian jaw. A secondary palate evolved twice in vertebrates in the archosaur lineage and in the synapsid lineage. In some therapsids, small, shelf-like extensions of bones (the hard palate) partially separated the nasal and oral passageways. The soft palate, a posterior extension of the secondary palate in animals, separates the mouth cavity from the nasal passages almost completely. Some mammals chew their food before ingesting it, like other vertebrates that do. The more extensive secondary palate allows mammals to breathe while chewing, Breathing needs to stop only briefly during swallowing (see figure 6).
  • 6. Teeth's arrangement and form are important indicators of mammalian lifestyle. In reptiles, the teeth are uniformly conical, a condition referred to as homodont. In mammals, the teeth are open and specialized for different functions, a condition called heterodont. Recall that in reptiles other than archosaurs, teeth were acrodont and attached along the top or inside of the jaw. In mammals ( as well as crocodylians) teeth is thecodont. That is, teeth are set into sockets of the jaw. For most of their lives, mammals have two sets of teeth. Deciduous or milk teeth, which appear before or soon after birth, are the first teeth. Permanent teeth come in to replace these missing pieces. The term "diphyodont condition" relates to this single tooth replacement. Adult mammals have up to four kinds of teeth. 1. Incisors Incisors are the most anterior teeth in the jaws. They are usually chisel-like and used for gnawing or nipping. 2. Canine Canine are often long, stour, and conical. They are usually for catching, killing, and tearing prey. The Canine and incisor have single roots.
  • 7. 3. Premolars Premolars are positioned next to the canine and have one or two roots and truncated surfaces for chewing. 4. Molars Molars have broad chewing surfaces and two (upper molars) or three (lower molars) roots. Mammalian species have a characteristic number of each kind of adult tooth. Zoologists use a dental formula to characterize taxa It is an expression of the number of teeth of each kind in one-half of the upper and lower jaws. The teeth of the upper jaws are listed below those of the lower jaws and in the following order: Incisors, Canine, Premolar, and Molars. For example: Human Beaver 2 ∙ 1 ∙ 2 ∙ 3 1 ∙ 0 ∙ 1 ∙ 3 2 ∙ 1 ∙ 2 ∙ 3 1 ∙ 0 ∙ 1 ∙ 3 Mammalian teeth (dentition) may be specialized for a particular diet. In some mammals, the dentition is reduced, sometimes to the point of having no teeth, For example, armadillos and the giant anteater (order Edentata) feed on termites and ants, and their teeth are reduced. Some mammals (e.g. humans, order primates; and pigs, order Artiodactyla) are omnivorous; they feed on a variety of plants and animal materials. They have teeth with flat grinding surfaces for rupturing plant cell walls in the back and teeth with sharp ripping and piercing surfaces in the front (see figure 7).
  • 8. Mammals that eat plant material often have flat, grinding posterior teeth and incisors, and sometimes have canines modified for nipping plant matter (e.g. horses, order Perissodactyla; deer, order Artiodactyla) or gnawing (e.g. rabbits, order Lagomorpha; beavers, order Rodentia) (figure 4b and c). In rodents, the incisor grows throughout life. Although most mammals have enamel covering the entire tooth, rodents have enamel only on the front of their incisors. The teeth are kept sharp by slower wear in front than in the back. A gap called the diastema separates the interior food-procuring teeth from the posterior grinding teeth. The diastema results from an elongation of the snout that allows the interior teeth to reach close to the ground or into narrow openings to procure food. The posterior teeth have a high, exposed surface (crown) and continuous growth, which allow these teeth to withstand years of grinding tough vegetation. Canines and incisors are used by predatory mammals to catch, kill, and tear prey. In members of the order Carnivora (e.g. coyotes, dogs, and cats), the fourth upper premolars and first lower molars form a scissor-like shearing surface, called the carnassial apparatus, that is used for cutting flesh from prey (figure 4d). The Vertebral Column The Vertebral column of mammals is divided into five regions. As with reptiles and birds, the first two cervical vertebrae are the atlas and axis. Five other cervical vertebrae usually follow. Even the giraffe and Whale have seven neck vertebrae, which are greatly elongated or
  • 9. compressed, respectively. In contrast, tree sloths have either six or nine cervical vertebrae, and the manatee has six cervical vertebrae. The trunk is divided into thoracic and lumber regions, as is the case for birds. In Mammals, the division is correlated with their methods of breathing. The thoracic region contains the ribs. Most ribs connect to the thoracic vertebrae and to the sternum via costal cartilages. Other ribs are attached only to the thoracic vertebrae or to the other ribs through cartilages. All ribs protect the heart and lungs. The articulation between the thoracic vertebrae provides the flexibility needed in turning, climbing, and lying on the side to suckle young. Lumber vertebrae have interlocking processes that give support, but little freedom of movement. Appendicular skeleton The appendicular skeleton of mammals rotates under the body so that the appendages are usually directly beneath the body. Joints usually limit the movement of appendages to the single anteroposterior plan, causing the tips of the appendages to move in long arcs. The bones of the pelvic girdle are fused in the adult, a condition that is advantageous for locomotion but presents problems during the birth of offspring. In a pregnant female, the ventral joint between the halves of the pelvis the public symphysis loosens before birth, allowing the pelvis to spread during birth. Muscles Most mammals, they generated the weight of the body because the appendages are located directly beneath the body. Upper appendages and girdles contain most of the body's muscle mass. Manny running mammals (e.g. deer order Artiodactyla) have little muscle in their lower leg that would slow leg movement. Instead, tendons run from muscles high in the leg to cause movement at the lower joints. ● Human respiratory system ● Endocrine System of Mammals ● The Heart and Circulatory system of Mammals