This document discusses locomotion in protozoa. It describes four types of locomotor organelles found in protozoa: pseudopodia, flagella, cilia, and pellicular contractile structures. It then discusses the four main methods of locomotion used by protozoa: pseudopodial movement, flagellar movement, ciliary movement, and metabolic movement. Flagellar movement involves three types of strokes: paddle stroke, undulating motion and simple conical gyration. Ciliary movement involves the rapid backward strokes of many cilia that push the protozoan forward. Metabolic movement is seen in certain flagellates and sporozoans and involves gliding, wriggling or peristaltic
DENTITION IN MAMMALS
The study of arrangement structure and number of types of teeth collectively is called as dentition. Teeth are present in the foetal as well as in adults of mammals, based on the presence of teeth Mammals are two types.
Edentata : In some animals teeth are absent hence called as edentate. e.g., Echidna or spiny ant-eater (Tachyglossus) the teeth are absent in all stages of life.
Dentata : Teeth are present in all mammals though a secon¬dary toothless condition is found in some mammals. Modern turtles and birds lack teeth. The adult platypus (Ornithorhynchus) bears epidermal teeth but no true teeth are present. In platypus embryonic teeth are replaced by horny epidermal teeth in adult.
Classification According to the Shape and Size of the Teeth:
Homodont:
Homodont or Isodont type of teeth is a condition where the teeth are all alike in their shape and size in the toothed whales e.g., Pinnipedians. Fishes, amphibians, reptiles and in the extinct toothed birds.
Heterodont
Heterodont condition is the usual feature in mammals, i.e. the teeth are distinguished according to their shape, size and function. The function is also different at different parts of the tooth row.
According to the Mode of Attachment of Teeth:
Thecodont : The teeth are lodged in bony sockets or alveoli of the jaw bone and capillaries and nerves enter the pulp cavity through the open tips of the hollow roots e.g., mammals, crocodiles and in some fishes.
Acrodont: The teeth are fused to the surface of the underlying jawbone. They have no roots and are attached to the edge of the jawbone by fibrous membrane e.g., fishes, amphibians and some reptiles.
Pleurodont:
The teeth are attached to the inner-side of the jawbone. The tooth touches the bone only with the outer surface of its root. In acrodont and pleurodont types of dentition, there are no roots, and nerves and blood vessels do not enter the pulp cavity at the base, e.g., Necturus (Amphibia) and some reptiles.
According to the Succession or Replace¬ment of Teeth:
DENTITION IN MAMMALS
The study of arrangement structure and number of types of teeth collectively is called as dentition. Teeth are present in the foetal as well as in adults of mammals, based on the presence of teeth Mammals are two types.
Edentata : In some animals teeth are absent hence called as edentate. e.g., Echidna or spiny ant-eater (Tachyglossus) the teeth are absent in all stages of life.
Dentata : Teeth are present in all mammals though a secon¬dary toothless condition is found in some mammals. Modern turtles and birds lack teeth. The adult platypus (Ornithorhynchus) bears epidermal teeth but no true teeth are present. In platypus embryonic teeth are replaced by horny epidermal teeth in adult.
Classification According to the Shape and Size of the Teeth:
Homodont:
Homodont or Isodont type of teeth is a condition where the teeth are all alike in their shape and size in the toothed whales e.g., Pinnipedians. Fishes, amphibians, reptiles and in the extinct toothed birds.
Heterodont
Heterodont condition is the usual feature in mammals, i.e. the teeth are distinguished according to their shape, size and function. The function is also different at different parts of the tooth row.
According to the Mode of Attachment of Teeth:
Thecodont : The teeth are lodged in bony sockets or alveoli of the jaw bone and capillaries and nerves enter the pulp cavity through the open tips of the hollow roots e.g., mammals, crocodiles and in some fishes.
Acrodont: The teeth are fused to the surface of the underlying jawbone. They have no roots and are attached to the edge of the jawbone by fibrous membrane e.g., fishes, amphibians and some reptiles.
Pleurodont:
The teeth are attached to the inner-side of the jawbone. The tooth touches the bone only with the outer surface of its root. In acrodont and pleurodont types of dentition, there are no roots, and nerves and blood vessels do not enter the pulp cavity at the base, e.g., Necturus (Amphibia) and some reptiles.
According to the Succession or Replace¬ment of Teeth:
ORIGIN OF CHORDATES
Animal kingdom is basically divided into two sub kingdoms:
Non-chordata- including animals without notochord.
Chordata- This comprising animals having notochord or chorda dorsalis.
Chordates were evolved sometime 500 million years ago during Cambrian period (invertebrates were also began to evolve in this period) .
Chamberlain (1900) pointed out that all modern chordates possess glomerular kidneys that are designed to remove excess water from body.
It is believed that Chordates have originated from invertebrates.
It is difficult to determine from which invertebrate group the chordates were developed.
Chordate ancestors were soft bodied animals. Hence they were not preserved as Fossils.
However, early fossils of chordates have all been recovered from marine sediments and even modern protochordates are all marine forms.
Also glomerular kidneys are also found in some marine forms such as myxinoids and sharks. That makes the marine origin of chordates more believable.
Chordates evolved from some deuterostome ancestor (echinoderms, hemichordates, pogonophorans etc.) as they have similarities in embryonic development, type of coelom and larval stages.
Many theories infers origin of chordates, hemichordates and echinoderms from a common ancestor.
It discusses basic information regarding a hemichordate animal called Balanoglossus or Acorn worm, which is also a good connecting link between the non-chordates and chordates.
are worm-like parasites. The clinically relevant groups are separated according to their general external shape and the host organ they inhabit. There are both hermaphroditic and bisexual species.
The definitive classification is based on the external and internal morphology of egg, larval, and adult stages.
Helminth is a general term meaning worm. The helminths are invertebrates characterized by elongated, flat or round bodies.
In flatworms or platyhelminths (platy from the Greek root meaning “flat”) include flukes and tapeworms.
Roundworms are nematodes (nemato from the Greek root meaning “thread”).
ORIGIN OF CHORDATES
Animal kingdom is basically divided into two sub kingdoms:
Non-chordata- including animals without notochord.
Chordata- This comprising animals having notochord or chorda dorsalis.
Chordates were evolved sometime 500 million years ago during Cambrian period (invertebrates were also began to evolve in this period) .
Chamberlain (1900) pointed out that all modern chordates possess glomerular kidneys that are designed to remove excess water from body.
It is believed that Chordates have originated from invertebrates.
It is difficult to determine from which invertebrate group the chordates were developed.
Chordate ancestors were soft bodied animals. Hence they were not preserved as Fossils.
However, early fossils of chordates have all been recovered from marine sediments and even modern protochordates are all marine forms.
Also glomerular kidneys are also found in some marine forms such as myxinoids and sharks. That makes the marine origin of chordates more believable.
Chordates evolved from some deuterostome ancestor (echinoderms, hemichordates, pogonophorans etc.) as they have similarities in embryonic development, type of coelom and larval stages.
Many theories infers origin of chordates, hemichordates and echinoderms from a common ancestor.
It discusses basic information regarding a hemichordate animal called Balanoglossus or Acorn worm, which is also a good connecting link between the non-chordates and chordates.
are worm-like parasites. The clinically relevant groups are separated according to their general external shape and the host organ they inhabit. There are both hermaphroditic and bisexual species.
The definitive classification is based on the external and internal morphology of egg, larval, and adult stages.
Helminth is a general term meaning worm. The helminths are invertebrates characterized by elongated, flat or round bodies.
In flatworms or platyhelminths (platy from the Greek root meaning “flat”) include flukes and tapeworms.
Roundworms are nematodes (nemato from the Greek root meaning “thread”).
. Cilia and flagella are the most prominent organelles associated with motility.
2. both are whip like and beat to move the microorganism
they differ from one another in two ways.
cilia and flagella are very similar in ultrastructure.
3. First, cilia are typically only 5 to 20 m in length, whereas flagella are 100 to 200 m long.
4. Second, their patterns of movement are usually distinctive.
5. Flagella move in an undulating fashion and generate planar or helical waves originating at either the base or the tip.
6. If the wave moves from base to tip, the cell is pushed along; a beat traveling from the tip toward the base pulls the cell through the water.
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Locomotry organelle & locomotion in protozoa
1. LOCOMOTION
• Locomotion is directional
movement that enables
someone or something to
move from one location to
another.
• The word derives from the
Latin words loco (place)
and motio (to move).
3. A. Pseudopodia
• Pseudopodia or false
feet are temporary
structures formed by
the streaming flow of
cytoplasm.
• Pseudopodia are of
the following types:
• Lobopodia
• Filopodia
• Reticulopodia
• Axopodia
4. 1. Lobopodia
• These are lobe-like pseudopodia with
broad and rounded ends, as in
amoeba.
• Composed of both ectoplasm as well
as endoplasm.
• Lobopodian move by pressure flow
mechanism.
5. 2. Filopodia
• These are more or less filamentous
pseudopodia
• Usually tapering form base to pointed
tip, as in Euglypha.
• Filopodia are composed of ectoplasm
only.
6. 3. Reticulopodia
• The reticulopodia are filamentous.
• Filament are branched and
interconnected.
• Reticulopodia display two-way flow of
cytoplasm.
7. 4. Axopodia
• They have needle like straight
pseudopodia.
• They contain a central axial rod which is
covered by granular and adhesive
cytoplasm.
• Axopodia display two-way flow of
cytoplasm.
• Axopodia are characteristic of heliozoans.
8. B. Flagella
• Flagella are the locomotor organelle
of flagellate protozoa, like euglena,
Trypanosoma, etc.
• A typical flagellum consist of an
axoneme.
• Axoneme arises from a basal
granule, the blepharoplast or
kinestosome.
• Fibers of axoneme remain
embedded in a fluid matrix.
9. • In axoneme, 9+2
arrangement is
present.
• Each peripheral pairs
bears a double row of
short arms, made of
protein called dynein.
• Peripheral paired fiber
is connected to inner
ring through radial
spoke.
10. Types of Flagella
• Stichonematic: Only one row of lateral
appendages.
• Pantonematic: Two or more rows of
lateral appendages.
• Acronematic: Lateral appendages are
absent and axoneme ends as a terminal
naked axial filament.
• Pantacronematic: Two or more rows of
lateral appendages and the axoneme
ends in terminal naked axial filament.
• Anematic: Simple without any lateral
appendages and a terminal naked
filament.
11. C. Cilia
• Cilia, characteristic of ciliata, they
also exhibit 9+2 structure.
• These are highly vibratile small
ectoplasmic processes.
• They are nine paired peripheral
fibers are enclosed within a
delicate sheath.
12. Basal granules show nine
peripheral subfibre triplets, each
disposed in a twist-like fashion.
Each cilium arises from a
thickened structure
blepharoplast.
One sub-fibre or microfibre of
each peripheral pair bears a
double row of short, projection,
called arms.
Basal Body/Centriole Forming
13. D. Pellicular Contractile
Structures
• In many Protozoa are found
contractile structures, in pellicle or
ectoplasm, called myonemes.
• These may be in the form of ridges and
grooves (e.g., Euglena), or contractile
myofibrils (e.g., larger ciliates), or
microtubules (e.g., Trypanosoma).
14. Method of Locomotion
i. Basically there are four known methods by which Protozoa
move:
ii. Pseudopodial movement,
iii. Flagellar Movement,
iv. Ciliary movement,
v. Metabolic movement.
15. i. Pseudopodial
Movement
• The pseudopodium is fixed
on the support by some
adhesive secretion and the
protoplasm of the body
gradually flows into it.
• The ectoplasm is dissolved
and the endoplasm flows.
• New Pseudopodia appear
and, by the repetition of the
process, the animal slowly
creeps forward
16. ii. Flagellar movement
• Three types of flagella movement have been recognized:
• Paddle Stroke: Common movement of a flagellum is
sideways lash, consisting of an effective down stroke and a
relaxed recovery stroke.
• Undulating Motion: Wave-like undulations in flagellum,
proceed from tip to base and from base to tip.
• Simple conical gyration: Bustchli’s screw theory postulates a
spiral turning of flagellum like screw. This exerts
propelling action , pulling the animal forward through
water.
17. iii. Ciliary Movement
• Some Protozoan’s move with the help of
cilia.
• Cilia are small hair-like structures, present
usually in large numbers on the body
surface.
• A cilium has a practically the same histology
as that of flagellum.
• The cilia act as small oars and the backward
strokes are swift, which push the animal
forward.
18. iv. Metabolic Movement
• This is a typical of certain flagellates (e.g. Euglena) and most sporozoans at certain stages
of their life cycles.
• Such organism are seen to show gliding or wriggling or peristaltic movement.
• Contractile myonemes or microtubules, present in their pellicular walls.
• Movement of this kind are also referred as gregarine movements.