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Latest Science NCERT Notes and Solutions (Class 11th)
Physics Chemistry Biology
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Physics Chemistry Biology

Class 11th (Biology) Chapters
1. The Living World 2. Biological Classification 3. Plant Kingdom
4. Animal Kingdom 5. Morphology Of Flowering Plants 6. Anatomy Of Flowering Plants
7. Structural Organisation In Animals 8. Cell : The Unit Of Life 9. Biomolecules
10. Cell Cycle And Cell Division 11. Photosynthesis In Higher Plants 12. Respiration In Plants
13. Plant Growth And Development 14. Breathing And Exchange Of Gases 15. Body Fluids And Circulation
16. Excretory Products And Their Elimination 17. Locomotion And Movement 18. Neural Control And Coordination
19. Chemical Coordination And Integration



Chapter 17 Locomotion And Movement



Movement is a fundamental characteristic of living beings, exhibited in a wide range of forms by both animals and plants. Some movements involve a change in location, which is called **locomotion**. While all locomotions are movements (change in position of the body or its parts), not all movements are locomotions (e.g., beating of heart, blinking of eyelids). Locomotion is typically performed for purposes like searching for food, shelter, mates, favorable conditions, or escaping enemies.

The structures used for locomotion are not always distinct from those used for other types of movements. For example, cilia in *Paramoecium* are used for both food movement and locomotion, and tentacles in *Hydra* are used for capturing prey and locomotion. Human limbs are used for changing body postures and locomotion.

Locomotion requires the coordinated activity of the muscular, skeletal, and neural systems. This chapter explores the types of muscles, their structure, the mechanism of muscle contraction, and the human skeletal system.

Types Of Movement

Cells in the human body exhibit three main types of movements:

Flagellar movement, similar to ciliary movement but typically involves longer structures, is also found in some cells (e.g., tail of spermatozoa for swimming) and organisms (*Euglena* for locomotion).



Muscle

**Muscle** is a specialized tissue of **mesodermal origin** that contributes significantly to body weight (40-50% in adult humans). Muscles have unique properties: **excitability** (respond to stimuli), **contractility** (shorten forcibly), **extensibility** (can be stretched), and **elasticity** (return to original shape after stretching/contracting).

Muscles are classified based on location, appearance, and regulation:

Let's examine skeletal muscle structure and contraction mechanism in detail:

Each skeletal muscle is made of **muscle bundles (fascicles)** held by fascia (connective tissue). Each fascicle contains muscle fibers (muscle cells). Each muscle fiber is a syncytium (multinucleated cytoplasm - **sarcoplasm**) lined by **sarcolemma** (plasma membrane). Sarcoplasmic reticulum (endoplasmic reticulum) stores calcium ions. Sarcoplasm contains many parallelly arranged filaments called **myofilaments** or **myofibrils**.

Each myofibril has alternate dark and light bands due to the arrangement of two main proteins: **Actin** (thin filaments) and **Myosin** (thick filaments).

Diagram showing the anatomy of a muscle fiber and a sarcomere, illustrating A bands, I bands, Z lines, M line, and H zone.

The portion of the myofibril between two successive Z lines is the functional unit of muscle contraction called the **sarcomere**.


Structure Of Contractile Proteins

Thin filament (Actin): Made of two filamentous (F) actins helically wound. Each F actin is a polymer of monomeric globular (G) actins. Two filaments of **tropomyosin** run along F actins. **Troponin**, a complex protein, is distributed at intervals on tropomyosin. In resting state, a troponin subunit masks the active binding sites for myosin on actin.

Diagram showing the structure of an actin (thin) filament with F-actin, tropomyosin, and troponin.

Thick filament (Myosin): Polymerized protein made of many monomeric **meromyosins**. Each meromyosin has a globular head with a short arm (Heavy Meromyosin, HMM) and a tail (Light Meromyosin, LMM). HMM component (head and short arm) projects outwards as a **cross arm**. The globular head is an active ATPase enzyme with binding sites for ATP and active sites for actin.

Diagram showing the structure of a myosin monomer (meromyosin) with HMM (head and short arm) and LMM (tail) components, and binding sites on the head.

Mechanism Of Muscle Contraction (Sliding Filament Theory)

Muscle contraction is explained by the **sliding filament theory**: thin actin filaments slide over thick myosin filaments, shortening the sarcomere.

Steps:

  1. Signal from CNS via motor neuron reaches the **neuromuscular junction** (motor-end plate). Neurotransmitter (Acetylcholine) is released.
  2. Acetylcholine generates an action potential in the sarcolemma, which spreads through the muscle fiber.
  3. Action potential causes release of **calcium ions (Ca$^{++}$)** from sarcoplasmic reticulum into the sarcoplasm.
  4. Increased Ca$^{++}$ level binds to troponin on actin filaments, changing its conformation and **unmasking the active binding sites** for myosin on actin.
  5. Myosin head binds to exposed active sites on actin, forming a **cross bridge**. This utilizes energy from ATP hydrolysis (myosin head is an ATPase).
  6. Cross bridge pulls the attached actin filaments towards the center of the A band (power stroke). Z lines attached to actins are pulled inwards, shortening the sarcomere (contraction). I bands reduce; A bands remain same length.
  7. Myosin releases ADP and Pi, goes to relaxed state. A new ATP molecule binds to myosin head, breaking the cross bridge.
  8. ATP is hydrolysed, myosin head cocks back, ready for next cycle. Cross bridge formation and breakage cycle repeats, causing further sliding.
Diagram illustrating stages of cross bridge formation, power stroke, and breaking of cross bridge during muscle contraction.

Process continues until Ca$^{++}$ ions are pumped back into sarcoplasmic reticulum, causing masking of actin binding sites by troponin. Cross bridges are broken, and muscles relax. The Z lines return to original position, sarcomere lengthens.

Diagram illustrating the sliding filament theory, showing relaxed and contracted sarcomeres with thin filaments sliding over thick filaments, affecting I band and H zone lengths.

Repeated muscle activation without sufficient oxygen can cause lactic acid accumulation (anaerobic glycogen breakdown) leading to fatigue.

Muscle fiber types:

Question 2. Define sliding filament theory of muscle contraction.

Answer:

The sliding filament theory of muscle contraction states that muscle contraction occurs due to the **sliding of the thin (actin) filaments over the thick (myosin) filaments** within the sarcomere. This sliding is driven by the formation and breaking of cross bridges between the myosin heads and the active sites on the actin filaments, powered by ATP hydrolysis. The sliding causes the sarcomere to shorten, resulting in the overall contraction of the muscle fiber.

Question 3. Describe the important steps in muscle contraction.

Answer:

Important steps in muscle contraction (based on the sliding filament theory):

  1. A neural signal arrives at the neuromuscular junction, releasing acetylcholine.
  2. Acetylcholine generates an action potential in the sarcolemma, which spreads and triggers the release of Ca$^{++}$ from the sarcoplasmic reticulum into the sarcoplasm.
  3. Ca$^{++}$ binds to troponin on the actin filaments, causing tropomyosin to move and expose the myosin binding sites on actin.
  4. Myosin heads bind to actin, forming cross bridges (using energy from ATP hydrolysis).
  5. The myosin head pivots, pulling the actin filament towards the center of the sarcomere (power stroke).
  6. A new ATP binds to the myosin head, breaking the cross bridge.
  7. Myosin head hydrolyses ATP and re-cocks, ready to bind again.
  8. Steps 4-7 repeat, causing continuous sliding, as long as Ca$^{++}$ is available.
  9. Muscle relaxes when Ca$^{++}$ is pumped back into the sarcoplasmic reticulum, masking the actin binding sites again.



Skeletal System

The **skeletal system** provides a framework of bones and cartilages that supports the body and facilitates movement. Bone and cartilage are specialized connective tissues; bone matrix is hard due to calcium salts, cartilage matrix is slightly pliable due to chondroitin salts. The human skeletal system has 206 bones and a few cartilages.

Divisions of the skeletal system:

Axial Skeleton components:

Diagrammatic view of the human skull, labelling cranial and facial bones, hyoid bone, and occipital condyles.
Diagram showing the vertebral column (right lateral view) with different regions labelled.
Diagram showing the ribs and rib cage structure.

Thoracic vertebrae, ribs, and sternum form the rib cage.

Appendicular Skeleton components:

Diagram showing the bones of the right pectoral girdle and upper arm.
Diagram showing the bones of the right pelvic girdle and lower limb.


Joints

**Joints** are essential points of contact between bones, or between bones and cartilages. They enable movement of bony parts, with the joint acting as a fulcrum and muscles generating the force. Movability varies between joints. Joints are classified structurally into three types:



Disorders Of Muscular And Skeletal System

Various disorders can affect the muscular and skeletal systems:



Exercises



Question 1. Draw the diagram of a sarcomere of skeletal muscle showing different regions.

Answer:

Question 2. Define sliding filament theory of muscle contraction.

Answer:

Question 3. Describe the important steps in muscle contraction.

Answer:

Question 4. Write true or false. If false change the statement so that it is true.

(a) Actin is present in thin filament

(b) H-zone of striated muscle fibre represents both thick and thin filaments.

(c) Human skeleton has 206 bones.

(d) There are 11 pairs of ribs in man.

(e) Sternum is present on the ventral side of the body.

Answer:

Question 5. Write the difference between :

(a) Actin and Myosin

(b) Red and White muscles

(c) Pectoral and Pelvic girdle

Answer:

Question 6. Match Column I with Column II :

Column I Column II
(a) Smooth muscle (i) Myoglobin
(b) Tropomyosin (ii) Thin filament
(c) Red muscle (iii) Sutures
(d) Skull (iv) Involuntary

Answer:

Question 7. What are the different types of movements exhibited by the cells of human body?

Answer:

Question 8. How do you distinguish between a skeletal muscle and a cardiac muscle?

Answer:

Question 9. Name the type of joint between the following:-

(a) atlas/axis

(b) carpal/metacarpal of thumb

(c) between phalanges

(d) femur/acetabulum

(e) between cranial bones

(f) between pubic bones in the pelvic girdle

Answer:

Question 10. Fill in the blank spaces:

(a) All mammals (except a few) have __________ cervical vertebra.

(b) The number of phalanges in each limb of human is __________

(c) Thin filament of myofibril contains 2 ‘F’ actins and two other proteins namely __________ and __________.

(d) In a muscle fibre $Ca^{++}$ is stored in __________

(e) __________ and __________ pairs of ribs are called floating ribs.

(f) The human cranium is made of __________ bones.

Answer: