Class 11 · Biology · Chapter 17 · NCERT Class 11 Biology

Locomotion and Movement Class 11 Notes

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Chapter mind map

The whole chapter at a glance: the big idea, then each branch and what sits under it.

Locomotion and Movement

Fundamental characteristics of life involving voluntary change of location and various cellular or tissue-level physical actions.

  1. Types of Movement

    Human body uses three main mechanisms: amoeboid, ciliary, and muscular movement for cellular and organ functions.

    • Cellular Mechanisms — Amoeboid (macrophages/leucocytes via pseudopodia), Ciliary (trachea/oviducts), and Muscular (limbs/tongue).
    • Locomotion Principles — Voluntary movement changing location. All locomotions are movements, but all movements are not locomotions.
  2. Muscle Tissue Properties

    Mesodermal tissue (40-50% body weight) with excitability, contractility, extensibility, and elasticity.

    • Skeletal Muscle — Striated, voluntary muscles attached to bones; primarily responsible for locomotion and posture changes.
    • Visceral and Cardiac — Visceral: smooth, involuntary (hollow organs). Cardiac: striated, branched, involuntary (heart).
  3. Muscle Structure

    Hierarchical organization from bundles to molecular filaments within the sarcoplasm.

    • Anatomical Hierarchy — Muscle contains fascicles (bundles) held by fascia; fascicles contain muscle fibres (syncitium) with myofibrils.
    • The Sarcomere — Functional unit between Z lines. Contains A-band (myosin), I-band (actin), M-line, and H-zone (non-overlap area).
  4. Contractile Proteins

    Complex proteins whose interaction facilitates the molecular basis of muscle contraction.

    • Actin (Thin) Filament — Composed of F-actin polymers, tropomyosin, and troponin which masks myosin-binding sites at rest.
    • Myosin (Thick) Filament — Polymer of meromyosin; HMM (head/short arm) has ATPase activity and actin-binding sites; LMM is the tail.
  5. Contraction & Fatigue

    Sliding filament theory and metabolic variations in muscle fibre types.

    • Sliding Filament Theory — CNS signal -> Acetylcholine -> Ca++ release -> Troponin binding -> Cross bridge formation -> Actin slides to M-line.
    • Fibre Types & Fatigue — Red (aerobic, high myoglobin/mitochondria) vs White (anaerobic, fast). Fatigue from lactic acid accumulation.
  6. Axial Skeleton

    80 bones along the main axis including skull, vertebral column, ribs, and sternum.

    • Skull and Hyoid — 22 bones (8 cranial, 14 facial) plus hyoid and 6 ear ossicles. Human skull is dicondylic.
    • Vertebrae and Ribs — 26 vertebrae (7C, 12T, 5L, 1S, 1Co). 12 pairs of ribs: 7 true, 3 false, 2 floating.
  7. Appendicular Skeleton

    Bones of the limbs (30 each) and the girdles that connect them to the axial skeleton.

    • Limbs — Forelimb: humerus, radius, ulna, carpals, metacarpals, phalanges. Hindlimb: femur, tibia, fibula, tarsals, patella.
    • Girdles — Pectoral (clavicle/scapula). Pelvic (two coxal bones fused from ilium, ischium, pubis) with pubic symphysis.
  8. Joints and Disorders

    Structural points of contact and clinical conditions affecting the locomotor system.

    • Joint Classification — Fibrous (none), Cartilaginous (limited), Synovial (ball-and-socket, hinge, pivot, gliding, saddle).
    • System Disorders — Myasthenia gravis, Muscular dystrophy, Tetany (low Ca++), Arthritis, Gout (uric acid), and Osteoporosis.

Chapter notes

An in-depth study of the mechanisms of movement in the human body, detailing the structure of muscles, the physiology of contraction, and the organization of the skeletal system and joints.

Understanding Movement and Locomotion

Movement is a fundamental characteristic of all living organisms, ranging from simple protoplasmic streaming to complex physical activities.

While all living beings exhibit movement, not all movements result in a change of location. Simple movements include the streaming of protoplasm in Amoeba or the movement of cilia and flagella in various microorganisms. In humans, we move our limbs, jaws, eyelids, and tongue for various daily functions.

Locomotion is a specific type of voluntary movement that results in a change of place or location. Examples include walking, running, climbing, flying, and swimming. It is important to note that the structures used for locomotion often serve other purposes as well. For instance, Paramoecium uses cilia for both moving food into its cytopharynx and for locomotion, while Hydra uses tentacles for capturing prey and movement.

The relationship between these two concepts can be summarized by the principle: all locomotions are movements, but all movements are not locomotions. Animals generally perform locomotion to search for food, shelter, mates, suitable breeding grounds, or to escape from predators.

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NCERT reference: chapter PDF page 1.

Types of Movement in Human Cells

The human body utilizes three primary mechanisms for cellular and tissue-level movement: amoeboid, ciliary, and muscular.

Amoeboid movement is exhibited by specialized cells like macrophages and leucocytes in the blood. This movement is achieved through the formation of pseudopodia (false feet) created by the streaming of protoplasm. Cytoskeletal elements, specifically microfilaments, play a crucial role in this process.

Ciliary movement occurs in internal tubular organs lined with ciliated epithelium. For example, the coordinated beating of cilia in the trachea helps filter out dust and foreign particles from inhaled air. Similarly, ciliary action facilitates the passage of ova through the female reproductive tract.

Muscular movement is the most prominent form in multicellular organisms, used for moving limbs, the tongue, and the jaw. This relies on the unique contractile property of muscle tissue. Effective locomotion requires the perfect coordination of the muscular, skeletal, and neural systems.

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NCERT reference: chapter PDF pages 1, 2.

Classification and Properties of Muscles

Muscle is a specialized tissue of mesodermal origin, making up 40-50% of an adult's body weight.

Muscles possess four key functional properties: excitability (responding to stimuli), contractility (shortening), extensibility (stretching), and elasticity (returning to original shape). They are classified based on their location, appearance, and how their activities are regulated.

Skeletal muscles are attached to bones and appear striped or 'striated' under a microscope. They are voluntary because they are under the conscious control of the nervous system. Visceral muscles, found in the walls of hollow organs like the digestive tract, are 'smooth' (non-striated) and involuntary, assisting in tasks like moving food.

Cardiac muscles are the muscles of the heart. They are striated like skeletal muscles but are branched and involuntary. The nervous system does not control their rhythmic activities directly.

FeatureSkeletal MuscleVisceral (Smooth) MuscleCardiac Muscle
LocationAttached to bonesInner walls of hollow organsHeart
AppearanceStriated (Striped)Non-striated (Smooth)Striated and Branched
ControlVoluntaryInvoluntaryInvoluntary
FunctionLocomotion/PostureTransportation of food/gametesPumping of blood

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Why are skeletal muscles called voluntary muscles?

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NCERT reference: chapter PDF pages 2, 3.

Structure of Skeletal Muscle and the Sarcomere

A skeletal muscle is a complex hierarchy of bundles and filaments designed for efficient contraction.

Each muscle is composed of multiple muscle bundles called fascicles, held together by a connective tissue layer called fascia. Within each fascicle are numerous muscle fibres (cells). Each muscle fibre is a syncitium, meaning it contains many nuclei within its sarcoplasm, and is enclosed by a plasma membrane called the sarcolemma.

The sarcoplasm contains parallelly arranged myofibrils, which show alternate dark and light bands. The light bands (I-bands) contain the protein actin, while the dark bands (A-bands) contain myosin. The I-band is bisected by an elastic 'Z' line, and the A-band is held together by an 'M' line.

The functional unit of contraction is the sarcomere, defined as the portion of a myofibril between two successive Z lines. In a resting state, the central part of the thick myosin filament not overlapped by thin actin filaments is known as the H zone.

Hierarchy of Muscle Organization

  1. 1

    Muscle

    The complete organ held together by fascia.

  2. 2

    Fascicle

    A bundle of muscle fibres within the muscle.

  3. 3

    Muscle Fibre

    The individual muscle cell containing sarcoplasm and nuclei.

  4. 4

    Myofibril

    Parallel filaments within the fibre showing striations.

  5. 5

    Sarcomere

    The functional unit between two Z lines containing actin and myosin.

This sequence shows the structural organization of skeletal muscle from the macroscopic level down to the functional molecular unit.

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What is the H zone in a sarcomere?

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NCERT reference: chapter PDF pages 3, 4.

Structure of Contractile Proteins

The interaction between actin and myosin proteins is the molecular basis for muscle contraction.

Actin (thin) filaments are composed of two 'F' (filamentous) actins wound helically. Each F actin is a polymer of 'G' (globular) actin monomers. Two other proteins are present: tropomyosin, which runs along the actin, and troponin, a complex protein distributed at intervals. In a resting state, troponin masks the binding sites for myosin on the actin filament.

Myosin (thick) filaments are also polymers, made of monomeric units called meromyosins. Each meromyosin has two parts: Heavy Meromyosin (HMM), consisting of a globular head and short arm, and Light Meromyosin (LMM), which is the tail.

The globular head of myosin is an active ATPase enzyme. It has specific binding sites for ATP and active sites to attach to actin, forming the 'cross arm' that facilitates movement.

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NCERT reference: chapter PDF page 5.

The Sliding Filament Theory

Muscle contraction is explained by the sliding of thin filaments over thick filaments, triggered by neural signals.

Contraction begins when the Central Nervous System (CNS) sends a signal via a motor neuron. At the neuromuscular junction, the neurotransmitter Acetylcholine is released, generating an action potential in the sarcolemma. This potential triggers the release of Calcium ions (Ca++) from the sarcoplasmic reticulum into the sarcoplasm.

The Calcium ions bind to troponin, removing the mask from the actin binding sites. Using energy from ATP hydrolysis, the myosin head binds to actin, forming a cross bridge. The myosin head then rotates, pulling the actin filaments toward the center of the A-band (the M-line).

This pulling action brings the Z-lines closer together, shortening the sarcomere and causing contraction. During this process, the I-bands reduce in size while the A-bands maintain their length. When a new ATP molecule binds to the myosin head, the cross bridge breaks, and the cycle repeats until Calcium is pumped back into storage, leading to relaxation.

  1. 1

    CNS sends signal via motor neuron to the neuromuscular junction.

  2. 2

    Acetylcholine release generates an action potential in the sarcolemma.

  3. 3

    Calcium ions are released from the sarcoplasmic reticulum into the sarcoplasm.

  4. 4

    Calcium binds to troponin, exposing active sites on actin filaments.

  5. 5

    Myosin head hydrolyses ATP and binds to actin to form a cross bridge.

  6. 6

    Myosin pulls actin filaments inward, shortening the sarcomere (contraction).

  7. 7

    New ATP binds to myosin, breaking the cross bridge for the next cycle.

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Which band changes length during muscle contraction?

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NCERT reference: chapter PDF pages 5, 6, 7.

Muscle Fatigue and Fibre Types

Muscles vary in their metabolic capabilities and endurance based on their pigment and organelle content.

Repeated muscle activation can lead to the accumulation of lactic acid due to the anaerobic breakdown of glycogen, resulting in muscle fatigue. This is a temporary state where the muscle's ability to contract diminishes.

Muscles are categorized into two types based on myoglobin, a red oxygen-storing pigment. Red fibres (Aerobic muscles) have high myoglobin content and many mitochondria. They utilize oxygen efficiently for ATP production and can sustain activity for long periods without fatiguing quickly.

White fibres have very little myoglobin and fewer mitochondria, giving them a pale appearance. They possess a high amount of sarcoplasmic reticulum and depend primarily on anaerobic processes for energy. These fibres are capable of fast, powerful contractions but fatigue rapidly.

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NCERT reference: chapter PDF page 7.

The Skeletal System: Axial Skeleton

The human skeletal system consists of 206 bones and some cartilages, divided into the axial and appendicular divisions.

The axial skeleton comprises 80 bones aligned along the body's main axis. It includes the skull, vertebral column, sternum, and ribs. The skull is composed of two sets of bones: 8 cranial bones that form the protective cranium and 14 facial bones. Additionally, a single U-shaped hyoid bone is located at the base of the buccal cavity, and each middle ear contains three tiny ear ossicles (Malleus, Incus, and Stapes).

The vertebral column consists of 26 serially arranged units called vertebrae: 7 cervical, 12 thoracic, 5 lumbar, 1 fused sacral, and 1 fused coccygeal. The first vertebra, the atlas, articulates with the skull's occipital condyles, making the human skull 'dicondylic'.

The rib cage is formed by 12 pairs of ribs, the sternum (breastbone), and thoracic vertebrae. Ribs 1-7 are 'true ribs', attached dorsally to the thoracic vertebrae and ventrally connected to the sternum with the help of hyaline cartilage. Ribs 8-10 are 'false ribs' (vertebrochondral) that join the 7th rib via hyaline cartilage, while ribs 11-12 are 'floating ribs' not connected ventrally.

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NCERT reference: chapter PDF pages 8, 9.

The Appendicular Skeleton

The appendicular skeleton includes the bones of the limbs and their supporting girdles.

Each limb consists of 30 bones. The forelimb (arm) includes the humerus, radius, ulna, 8 carpals (wrist), 5 metacarpals (palm), and 14 phalanges (digits). The hindlimb (leg) includes the femur (longest bone), tibia, fibula, 7 tarsals (ankle), 5 metatarsals, and 14 phalanges, plus the patella (knee cap).

The pectoral girdle (shoulder) consists of the clavicle (collar bone) and scapula (shoulder blade). The scapula features a glenoid cavity that articulates with the humerus. The pelvic girdle (hip) is formed by two coxal bones, each created by the fusion of the ilium, ischium, and pubis.

The two halves of the pelvic girdle meet ventrally at the pubic symphysis, which contains fibrous cartilage. The acetabulum is the cavity in the pelvic girdle where the femur attaches.

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NCERT reference: chapter PDF pages 9, 10.

Classification of Joints

Joints are points of contact between bones or between bones and cartilage, acting as fulcrums for movement.

Fibrous joints allow no movement. An example is the sutures between the flat bones of the skull that fuse end-to-end with the help of dense fibrous connective tissues to form the cranium. Cartilaginous joints allow limited movement, such as the joints between adjacent vertebrae in the spinal column.

Synovial joints are characterized by a fluid-filled synovial cavity between articulating surfaces, allowing for considerable movement and locomotion. There are several types: Ball and socket (shoulder/hip), Hinge (knee/elbow), Pivot (atlas/axis), Gliding (carpals), and Saddle (thumb).

The degree of movability depends on the structural arrangement and the presence of synovial fluid, which reduces friction between articulating surfaces.

Joint TypeMovement LevelExample
FibrousNoneSkull sutures
CartilaginousLimitedBetween vertebrae
Ball and SocketConsiderable movementShoulder (Humerus/Scapula)
HingeConsiderable movementKnee joint
PivotConsiderable movementBetween Atlas and Axis
SaddleConsiderable movementCarpal and Metacarpal of thumb

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NCERT reference: chapter PDF pages 10, 11.

Disorders of the Muscular and Skeletal Systems

Various conditions can affect the functionality of muscles and bones, ranging from genetic disorders to hormonal imbalances.

Myasthenia gravis is an autoimmune disorder that targets the neuromuscular junction, causing fatigue and paralysis of skeletal muscles. Muscular dystrophy is a progressive genetic degeneration of skeletal muscles.

Tetany involves wild, rapid muscle contractions caused by low calcium levels in body fluids. Arthritis is the general inflammation of joints, while Gout is a specific type of inflammation caused by the accumulation of uric acid crystals.

Osteoporosis is an age-related disorder where bone mass decreases, increasing fracture risk. It is often linked to decreased estrogen levels in older individuals.

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NCERT reference: chapter PDF page 11.

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