Professional Documents
Culture Documents
Animal Species
Chordata
Arthropoda Other
2%
87% 12%
Cnidaria
1%
Platyhelminthes
1%
Nematoda
1%
Annelida
1%
Porifera
1%
Echinodermata
1%
~ Characteristics ~
Multicellular
Heterotrophs (consumers)
~ Characteristics ~
Have a nervous system to respond to their
environment
No backbones
live in water
no symmetry
Live in water
Medusa - like a
jellyfish
Polyp - like a
hydra
~Invertebrate
Phylum Cnidaria~
Examples -
Jellyfish, Hydra,
sea anemones, and
corals
~Invertebrate
Phylum Platyhelminthes ~
Flatworms
bilateral symmetry
~Invertebrate
Phylum Platyhelminthes ~
Examples: Planaria
Parasite that
lives in intestines
of host
absorbing food
~Invertebrate
Phylum Platyhelminthes ~
Examples: Fluke
parasite
lives inside
of host
~Invertebrate
Phylum Nematoda ~
Roundworms
– small or microscopic
– bilateral symmetry
– Trichinella
~Invertebrate
Phylum Mollusca ~
Soft bodies
Hard Shells
– stomach-footed -
move on stomach
~Invertebrate
Phylum Mollusca ~
Class Bivalves
– 2 shells hinged
together
– clams, oysters,
scallops and
mussels
~Invertebrate
Phylum Mollusca ~
Class Cephalopods
–internal mantel
~Invertebrate
Phylum Annelida ~
–Segemented worms
– Live in water or
underground
Radial symmetry
endoskeleton
~Invertebrate
Phylum Echinodermata ~
Examples: seastar, sea urchin, sand dollar
and sea cucumber
~Invertebrate
Phylum Arthropoda ~
Body divided into sections/segments
Exoskeleton
Jointed legs
no antennae
4 pairs of legs
Horseshoe crabs
– Ancient group of species
2 antennae
no antennae
3 pairs of legs
Millipedes
segmented animals
Class Chiopoda
GNATHOSTOMATA
Characteristics
– internal jaws (palatoquadrate, Meckel's cartilage) are present.
– paired appendages (paired pectoral and pelvic fins) supported by
an internal skeleton provide more efficient locomotion
– three semicircular canals
– teeth - modified dermal scales
– more proficient predators than the jawless fish
Taxa
– the jawed vertebrates include the extinct ,armored Placoderms,
the cartilaginous fish, and the bony fish (including the
tetrapods).
– Phylogenetic relationships of the jawed fishes
Characteristics
Characteristics :
gills close behind braincase (primitive)
jaw support autostylic (holostylic)
dentition a small number of large,
continuously growing tooth plates
fin structures similar to sharks
Characteristics
Subclass Actinopterygii
ray-finned fish
most fish (most vertebrates)
Subclass Sarcopterygii
fleshy-finned fishes
lungfish and coelacanth
fleshy finned fish gave rise to amphibians in the Devonian
Class OSTEICHTHYES
Class AMPHIBIA
5,500 species
Amphibians today include salamanders,
toads and frogs (the Lissamphibia)
Paleozoic amphibians gave rise to the
amniotes
Class AMPHIBIA
Order Gymnophiona (Apoda)---Caecilians
elongate bodies, limbless, scales in annular folds
of skin
Order Caudata (Urodela)---salamanders
tailed, usually with two pairs of limbs
Order Anura (Salienta)---frogs and toads
tailless, elongate hindlimbs, head and trunk
fused
SUBCLASS LISSAMPHIBIA
Ectotherms
Amphibians shed eggs in water for external fertilization (not fully
adapted to land)
Eggs first evolve as aquatic larvae with external gills, then undergo
metamorphosis to emerge from water as adults
They have thin skin (needed gas exchange), thus in danger of
desiccation if removed from a moist/wet environment
Amphibians gave rise to amniotes during the Pennsylvanian Period
All living amphibians are carnivorous; will eat anything they catch;
no morphological specializations related to diet.
Amphibian populations are undergoing dramatic declines, which has
been attributed to ultraviolet radiation, environmental toxins,
etc. Parasites have been identified as the cause of deformities in
frogs.
Classification
The 5500 species of amphibians are
grouped into 3 orders:
Salamanders (order Caudata or Urodela)
Frogs and toads (order Anura or Salientia)
The secretive, earthworm-like tropical
caecilians (order Gymnophiona or Apoda)
- limbless amphibians.
ORDER URODELA [CAUDATA]
Ambystoma tigrinum
Characters
least specialized of all living amphibians
elongate body
simple primitive limbs, set at right angles to body; most
have 4 limbs but a few aquatic species have only 2
limbs.
locomotion similar to that of primitive tetrapods--lateral
bending (fishlike) plus leg movement
aquatic, semi-aquatic, terrestrial
paedomorphosis is common in aquatic salamanders
terrestrial salamanders live in moist places under stones
and rotten logs, usually not far from water
Diet
Hyla cinerea
Bufonidae - toads
– paratoid gland present
– Poisonous skin secretion,
– some species can kill dogs
– e.g., Bufo alvarius
Bufo marinus
Pelobatidae
– Spadefoot toads
Scaphiopus
Other families
Rhinophrynidae
– Rhynophrynus dorsalis Mexican burrowing frog
– Weak hind legs, doesn't hop
– Burrows in termite nests, rotten logs
– Usually collected at ponds when breeding.
– Male calls while floating in middle of pond
Pipidae
– Africa and S. America, Aquatic
– examples: Suriname toad Pipa pipa, African clawed frog, Xenopus
Dendrobatidae
– Arrow-poison frog--Neotropical
Ex. Dendrobates tinctorius Dye frog
ORDER GYMNOPHIONA
[APODA]
caecilians
– members of an obscure order called
Gymnophiona (naked snake). 160 species of
worm-like amphibians.
– Found in tropical forests of South America
(primarily), Africa, and south-east Asia.
Ichthyophis bannanicus
Characters
limbless
– an early Jurassic caecilian possesses limbs
mostly burrowing species, some aquatic
solidly built skull
long, slender--body up to 200 vertebra
small dermal scales
no postanal tail
many species are blind as adults, have the name
caecilians (caecus, blind). Because they are burrowers,
the eyes are replaced by specialized sensory tentacles on
the snout. Very rarely seen due to their burrowing
nature.
Class REPTILIA
7,800 species
Turtles, crocodiles, lizards, snakes, etc.
Reptile lungs are efficient, don't use skin
for gas exchange
They have internal fertilization and
produce eggs with leathery shells
Class REPTILIA
Reptiles have acquired several advances over
amphibians that have allowed them to move successfully
into terrestrial habitats.
Their skin, for example, is more heavily cornified and is
protected with surface scales that are impervious to
water.
To help conserve water the kidney produces a
concentrated urine, and the volume has been reduced.
Since reptiles have internal fertilization, water isn't even
needed for mating.
The eggs have undergone extensive modification
compared to those of amphibians and are termed
cleidoic eggs.
Class REPTILIA
Reptiles have three extraembryonic membranes the chorion, amnion
and allantois. The amnion is a fluid-filled sac that encloses the
embryo, providing it with its own private pond. The chorion and
allantois are vascularized membranes that lie against the shell. The
allantois develops as an outgrowth of the hindgut.
It helps with respiration and serves as a Johnny-on-the-spot for the
developing embryo. The chorion is the outermost extraembryonic
membrane and is mainly concerned with respiration. These
membranes are surrounded by albumen, and then a shell. The egg
shell is porous and either leathery or limy.
This adaptation allows respiration through the shell without losing
too much water.
On the down side, most reptile eggs become waterlogged if exposed
to water for too long.
Females usually lay their eggs, but some lizards and snakes retain
them for internal development.
Class REPTILIA
To keep up with their greater activity there are changes in
reptiles' pelvic and pectoral girdles to make them strong
Some even have four-chambered hearts with separate
pulmonary and systemic circulations.
Respiration is by lungs, although cloacal respiration can act
as an auxiliary system in some aquatic turtles.
Many reptiles adjust their body temperature by behavioral
mechanisms, basking in the sun to warm up in the morning
and then seeking shelter in the heat of the day.
Physiological mechanisms sometimes aid in this behavioral
thermoregulation: Chromatophores can open to darken the
skin so that it absorbs more heat, and blood flow to the skin
can be regulated.
Class REPTILIA
The first reptiles were amphibian-like
beasts called cotylosaurs appeared during
the Carboniferous period (about 350
million years before present).
Turtles are most similar to the cotylosaurs
(although the latter did not have shells)
and are placed in the same subclass.
A turtle’s body is covered on the dorsal
surface by a bony shell with horny plates
Class REPTILIA
Alligators, have jaws that house teeth that are
all alike, albeit of differing size (homodont
dentition).
The conical the codont teeth are set in sockets
called alveoli in the premaxillae, and dentary
(lower jaw).
The alligator skull has a large number of cranial
bones and in this respect is more primitive than
that of the frog (even though reptiles evolved
after the amphibians).
Class REPTILIA
A reptile's scales are very different in structure from that of fish.
The outer layer of skin is the thick stratum corneum (thick layers of
dead, keratin-filled cornified cells).
These cells are organized into horny scales covering the entire
outer surface.
The scales are important in protecting the animal from abrasion and
drying out.
The plates making up the shell of turtles are composed of a similar
material.
Hinges between the scales permit flexible movements.
The lower epidermis, like that of amphibians, is the stratum
germinativum (it produces the upper cell layers).
Unlike the amphibians, there are few skin glands.
Class AVES
9,100 species
Characteristics
– Birds have internal fertilization and lay hard-shelled
eggs
– Endotherms
– Nearly every anatomical feature is related to ability to
fly
The only animals with feathers (modified reptilian scales)
– Many types of birds exist:
flightless; web footed; divers; waders; vegetarian; etc
Class AVES
Birds are endothermic (warm-blooded)
vertebrates with feathers.
Their anterior limbs are modified as wings for
flight, while the posterior pair is adapted for
walking, swimming, or perching.
Other adaptations related to flight include
changes in the skeletal, respiratory, circulatory,
reproductive, digestive, and excretory systems.
Class AVES
The first birds arose from saurishian dinosaurs
during the Jurassic (about 180 million years
before present).
Today's birds still retain many reptilian
characteristics such as similarities in behavior,
skull structure, and scales on their beak, legs,
and feet. Birds have been incredibly successful
(among the chordates, they are outnumbered
only by the bony fish).
Subclass Archaeornithes
The Archaeornithes, are represented by a single extinct
species (Archaeopteryx). The first Archaeopteryx
specimen was discovered during the nineteenth century.
It was about the size of a crow, had a long reptilian tail,
thecodont teeth, and a reptilian skull with no beak. It
had three fingers on its wings, each bearing a claw.
Because of its small sternum and flexible trunk, it's
unlikely that Archaeopteryx was a strong flier.
Its characteristics are so reptilian that, were it not for
the feathers fossilized with the specimen, it would not be
recognizable as a potential ancestor of birds. Protoavis, a
smaller animal discovered in 1986, may be more closely
allied to today's birds).
Subclass Archaeornithes
Archaeopteryx
Subclass Neornithes
All birds other than Archaeopteryx belong to the subclass
Neornithes.
While most neornithes fly, ratites can not. Examples of
living ratites include emus, rheas, ostriches, and
penguins.
Neornithes that fly are carinates (they have a large
carina).
The largest living carinate is the Andean condor, with a
wing span of about 3 meters.
The condor, by no means, represents a limit on size for
birds (the giant Teratorn had a wingspan of 8 meters).
Modifications Related to Flight.
The long bones are thin and slender.
Likewise, the skull is thin.
Teeth have been lost and replaced by a light beak.
Many bones lost their central marrow and are now hollow and
porous.
The reduction in the number of bones of the wrist.
The sternum has broadened into a wide keel to provide a base
for attachment of wing musculature. Many bones are fused.
Those of the pelvis are fused to the lower vertebrae of the
back, while the ribs are joined to the vertebrae and sternum.
This consolidation insures that birds don't have to expend
muscular energy to hold their lower body straight during flight.
Subclass Neornithes
Subclass Neornithes
The lungs are directly attached to the ribs and
have air sacs that extend into the bones.
Both of these attributes raise ventilation
efficiency to keep up with their increased
metabolic needs.
They have no urinary bladder and a short large
intestine (to cut back on weight).
The cerebral hemispheres and cerebellum show
a dramatic increase in size over the reptiles to
permit more complex behaviors and coordination
needed for flight.
Avian Feathers and Skin
Feathers are cornified epidermal appendages that are probably related to
scales. They are used for thermoregulation, communication, and as a flight
surface.
There are three varieties of feathers: contour feathers, down feathers
(plumules), and plumes (hairlike feathers).
The main axis of the feather is divided into a hollow calamus that inserts
into the animal's skin at a feather follicle and a rachis flattened is attached
to the shaft and makes up the main flight surface.
The vane is built from numerous barbules.
The barbules attach to hooklets on adjacent barbs to hold together the
vanelike structure of the feather.
If the barbs become separated, the bird zips them back together by
preening.
Contour feathers that form the flight surfaces are called flight feathers.
Down feathers provide excellent insulation because numerous fluffy barbs
at the quill tip trap insulating air.
Avian Feathers and Skin
Feather development begins when mesodermal tissue in
the dermis produces a pimply feather primordium.
The feather primordium elongates toward the epidermis,
forming a feather follicle.
Cells at the base of the follicle then begin to grow
forming a feather sheath within which is formed an
immature feather.
The feather sheath and immature feather together make
up a pin feather.
Eventually, the feather sheath splits open and releases
the barbs, and then the remainder of the feather.
Class MAMMALIA
4,800 species
mammals evolved in the late Triassic, the time dinosaurs
first appeared.
mammals diversified greatly following the extinction of
the dinosaurs during the Cenozoic
Characteristics
– hair - protection from heat loss
– mammary glands
– differentiated teeth
– endotherms; 4 chambered heart; etc.
– Greatest size range
pigmy shrew to blue whale
Characteristics
Members of the class Mammalia possess both hair and mammary
glands.
Their integument is complex and has many glands used for a variety of
purposes: thermoregulation and excretion (sweat glands),
communication (scent glands), care of the hair and skin (sebaceous oil
glands), and for feeding of the young (mammary glands).
They are thermic and have relatively high rates of metabolism. In
keeping with their higher metabolic rates, adaptations for efficient
feeding include heterodont teeth in most species and a secondarypalate
to separate the respiratory and food passages (so they can breathe and
chew at the same time).
The circulatory systems are efficient, and they have a four-chambered
heart with separate pulmonary and systemic circulations. Their brains
are highly developed, fertilization is internal, and most have placental
attachment of the young.
Subclass Theria
Most living mammals belong to the
subclass Theria (placental mammals) and
are thought to have developed from
mammallike reptiles called therapsids
during the Mesozoic (about 180 million
years ago).
The placentals are extremely diverse,
occupying all habitable environments on
earth.
Subclass Prototheria
Members of the subclass Prototheria are so different from placentals that
they may have developed from a different theriapsid species.
They are represented today by only a single order, Monotreme (egg-laying
mammals).
Today's monotremes are found in Australia, Tasmania, and New Guinea.
The only living monotremes are the duckbill platypus and echidna (spiny
anteater).
Monotremes have several primitive characteristics: They lack teeth as
adults, the braincase and other skeletal elements are reptilian in structure,
they have a single ventral orifice (connected to a cloaca), and they are
oviparous.
Although they are homothermous, their body temperature is maintained
only a few degrees above the ambient temperature.
In these ways they are reptilian in their structure, reproduction, and
physiology. Nonetheless, monotremes do possess hair and feed their young
milk, so they do qualify as mammals.
Subclass Theria,
Infraclass Metatheria
Metatherians are the marsupial mammals (kangaroos, koalas,
opossums, Tasmanian wolves, and wombats).
Like the placental mammals (superclass Eutheria), marsupials start
their lives attached by a placenta to the maternal circulation.
Although the embryo and maternal circulation do not mix, the
developing young receive nutrients and discharge metabolic wastes
through the placenta.
Marsupial placental development, however is short-lived; and
following their birth the embryos attach to a nipple within a skin
pouch (marsupium) where they continue their development.
The most common American opossum is Didelphis virginiana. They
are nocturnal in their habits and are often found in association with
humans.
Subclass Theria,
Infraclass Eutheria
Eutherian mammals, including yourself, are placental beasts and belong to
the infraclass Eutheria.
Among the lower vertebrates the teeth are simple in structure and usually
similar in shape.
Mammals, however, have teeth adapted to different food-processing
functions.
These teeth are classified from front to back as incisors, canines, premolars,
and molars. Incisors are usually small spindle-shaped teeth used for cutting,
chopping, and picking up food (although in rodents they are greatly
enlarged). Canines are sharp conical teeth useful for seizing prey and
tearing flesh. The development of canine teeth varies with the diet of the
animal. They are usually poorly developed or absent in herbivores and are
especially well developed in carnivorous mammals. Sometimes there is
variation according to sex (males having larger canines), while in other
species they grow to become premolars and molars are collectively known
as cheek teeth. Premolars are often used to puncture food while the
broader molars are involved in crushing and grinding food. Depending on
the diet, the premolar teeth may broaden to look much like the molars. The
occlusion between the upper and lower cheek teeth forms efficient surfaces
between which food can be cut, crushed, or torn according to their
structure.
Subclass Theria,
Infraclass Eutheria
The number and arrangement of the teeth are important in the
classification of mammals. A convenient way of expressing this arrangement
is through a dental formula that depicts the number of teeth in each half
jaw. For the primitive condition, the upper jaw has three incisors, one
canine (fang), four premolars, and three molars. The lower jaw has the
same arrangement. Because of this ancestral arrangement, mammals
usually have 44 teeth at most. However, because of secondary
modifications some species have no teeth (monotremes) while others have
several hundred (dolphins). This primitive arrangement is modified to one
degree or another amomg and within the various orders.
Among the carnivores, all teeth are represented. Using dogs as an example,
they differ from the primitive condition only in a missing molar on the upper
jaw. For carnivores, the important aspect of these dental formulae is that all
four types of teeth are represented.
The structure of the teeth is also important in classification of mammals,
but this aspect of taxonomy is more complicated and will not be covered
here. It may seem terribly superficial to classify mammalian orders based
on tooth structure, but since the teeth are related to feeding, they are
representative of other differences in anatomy and physiology.
Order Carnivora
Carnivores are predatory mammals with clawed
feet and teeth adapted for cutting flesh although
some carnivores have secondarily taken on an
omnivorous habit).
Carnivores are among the brightest and
strongest of animals.
Examples of carnivores include badgers, bears,
foxes, otters, raccoons, skunks, weasels,and
wolves.
Order Primates
Members of this order are mainly arboreal
(living in trees), although some, like
ourselves, have moved to the ground.
They have five digits on their front and
hind legs, usually adorned with nails,
rather than claws.
They include such beasts as apes,
gibbons, lemurs, monkeys, tree shrews,
and humans.
Order Rodentia
This is a very successful order since nearly half of living
mammalian species are classified as rodents. All rodents
have large chisellike incisors and lack canines and
premolars.
Examples of rodents include beavers, lemmings,
marmots, mice, prairie dogs, rats, squirrels, and voles.
The dental structure of all rodents is similar. They have
large incisors, and the major differences are in the
grinding surfaces of the molars.
The lower incisors continuously grow and must be
trimmed by gnawing.
Order Lagomorpha
Fish
Rodents
Terimakasih
Marsupials
Primates
Reptiles Whales and Dolphins