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Body Fluids and Circulation

NCERT Class 11 · Biology Based on NCERT Class 11 Biology textbook · Free CBSE study kit

Chapter Notes

LOCOMOTION AND MOVEMENT

Definitions and Key Concepts

**Movement** is the change in position or place of an organism or body part. It is one of the significant features of all living beings.

**Locomotion** is a specific type of voluntary movement that results in a change of place or location of the whole organism. Examples: walking, running, climbing, flying, swimming.

Key distinction: **All locomotions are movements, but all movements are not locomotions.** For example, chewing food is movement but not locomotion.

Movement occurs for several biological reasons:

  • Search for food
  • Finding shelter
  • Finding mates
  • Locating suitable breeding grounds
  • Seeking favorable climatic conditions
  • Escaping from enemies or predators
  • Structural and Functional Relationships

    Locomotory structures are often multifunctional. The same structure may perform different functions:

  • **Cilia in Paramoecium**: Move food through cytopharynx AND facilitate locomotion
  • **Tentacles in Hydra**: Capture prey AND assist in locomotion
  • **Limbs in humans**: Change body posture AND enable locomotion
  • The mode of locomotion varies with:

  • Animal's habitat (aquatic, terrestrial, aerial)
  • Situational demands
  • Evolutionary adaptations
  • ---

    TYPES OF MOVEMENT

    Human cells exhibit **three main types of movement**:

    1. Amoeboid Movement

    **Definition**: Movement involving the formation of temporary cytoplasmic projections called **pseudopodia** (false feet), formed by streaming of protoplasm.

    **Mechanism**:

  • Involves cytoskeletal elements, particularly **microfilaments** (actin and myosin)
  • Protoplasm flows from one end of the cell to the other
  • Temporary extensions of the cell membrane form pseudopodia
  • Cell body follows the pseudopodia
  • **Cells showing amoeboid movement**:

  • Leucocytes (white blood cells) in blood
  • Macrophages in connective tissues
  • Free-living amoebae (Amoeba proteus)
  • **Biological significance**:

  • Enables cell migration
  • White blood cells can reach infected areas
  • Important in immune response
  • 2. Ciliary Movement

    **Definition**: Movement caused by coordinated beating of hair-like structures called cilia projecting from the cell surface.

    **Location in human body**:

  • Trachea and bronchi (respiratory tract)
  • Fallopian tubes (female reproductive tract)
  • Inner lining of ventricles of brain
  • Kidney tubules
  • **Mechanism**:

  • Cilia beat in coordinated waves
  • Each cilium has a power stroke and recovery stroke
  • Cilia are made of microtubules arranged in 9+2 pattern (as studied in Chapter 8)
  • **Biological functions**:

  • **In trachea**: Removes dust particles and foreign substances inhaled with air; protects lungs
  • **In female reproductive tract**: Facilitates passage of ovum toward uterus
  • **In brain ventricles**: Facilitates cerebrospinal fluid circulation
  • **In kidney tubules**: Assists in fluid movement
  • 3. Muscular Movement

    **Definition**: Movements caused by contraction and relaxation of muscles, a specialized contractile tissue.

    **Characteristics of muscles**:

  • Specialized tissue of **mesodermal origin**
  • Contributes **40-50% of human body weight** in adults
  • Possess four major properties:
  • **Excitability**: Respond to neural stimulation
  • **Contractility**: Can shorten and develop tension
  • **Extensibility**: Can be stretched
  • **Elasticity**: Return to original length after stretching
  • **Functions**:

  • Locomotion
  • Changes in body postures
  • Movement of specific body parts (jaw, eyelids, tongue, limbs)
  • ---

    MUSCLE

    Classification of Muscles

    Muscles are classified based on three criteria: **location, appearance, and regulation of activity**.

    #### A. Skeletal (Striated Voluntary) Muscles

    **Location**:

  • Attached to skeletal components (bones and cartilages)
  • Cover the external surface of the body
  • Form the musculature of limbs
  • **Appearance**:

  • Exhibit **striped or striated pattern** under microscope due to alternating light and dark bands
  • Pattern is due to regular arrangement of contractile proteins
  • **Regulation**:

  • Under **voluntary control** of the central nervous system (CNS)
  • Also called **voluntary muscles**
  • **Function**:

  • Primary role in locomotory actions
  • Changes in body posture
  • Precise, powerful movements
  • **Structure**:

  • Made of muscle fibers arranged in bundles
  • Each fiber is multinucleate (syncytium)
  • #### B. Visceral (Smooth Involuntary) Muscles

    **Location**:

  • Inner walls of hollow visceral organs
  • Alimentary canal (esophagus, stomach, small intestine)
  • Reproductive tract
  • Blood vessels
  • Urinary bladder
  • **Appearance**:

  • Smooth, non-striated appearance under microscope
  • Also called **smooth muscles** or **non-striated muscles**
  • **Regulation**:

  • **NOT under voluntary control**
  • Controlled by autonomic nervous system
  • Also called **involuntary muscles**
  • **Function**:

  • Transportation of food through digestive tract (**peristalsis**)
  • Movement of gametes through reproductive tract
  • Regulation of blood vessel diameter
  • Movement of materials through ducts
  • **Structure**:

  • Fibers are uninucleate or binucleate
  • Spindle-shaped fibers
  • #### C. Cardiac Muscles

    **Location**:

  • Heart walls exclusively
  • **Arrangement**:

  • Multiple cardiac muscle cells assemble in **branching patterns**
  • Connected by intercalated discs containing tight junctions
  • **Appearance**:

  • **Striated** (similar to skeletal muscles)
  • However, striations are less regular than skeletal muscles
  • **Regulation**:

  • **Involuntary** in nature
  • CNS does not directly control their activity
  • Possess autorhythmicity (can contract without external stimulus)
  • **Function**:

  • Pumping of blood throughout the body
  • Maintaining continuous circulation
  • ---

    STRUCTURE OF SKELETAL MUSCLE

    Hierarchical Organization

    Skeletal muscles have a precise hierarchical organization from gross to microscopic level:

    **Level 1: Whole Muscle**

  • Multiple muscle bundles held together by **fascia** (collagenous connective tissue sheath)
  • Fascia extends from the muscle to form tendons that attach to bones
  • **Level 2: Muscle Bundle (Fascicle)**

  • Bundle of muscle fibers
  • Surrounded by **perimysium** (connective tissue layer)
  • **Level 3: Muscle Fiber (Muscle Cell)**

  • Single elongated multinucleate cell
  • **Sarcolemma**: Plasma membrane surrounding the muscle fiber
  • **Sarcoplasm**: Cytoplasm of muscle fiber containing:
  • Multiple nuclei (syncytium)
  • Mitochondria
  • Sarcoplasmic reticulum (specialized endoplasmic reticulum)
  • Myofibrils (contractile filaments)
  • **Level 4: Myofibril (Myofilament)**

  • Parallel cylindrical structures within sarcoplasm
  • Made of thick and thin filaments
  • **Level 5: Sarcomere**

  • **Functional unit of muscle contraction**
  • Portion of myofibril between two successive Z-lines
  • Contains contractile proteins arranged in specific patterns
  • Banding Pattern of Myofibril

    Under electron microscope, myofibrils show alternating dark and light bands due to overlapping arrangement of actin and myosin filaments:

    **I-Band (Isotropic Band)**

  • Appears **light** in color
  • Contains only **thin (actin) filaments**
  • Bisected in the middle by an elastic fiber called **Z-line** or **Z-disc**
  • During muscle contraction, I-band length **decreases**
  • **A-Band (Anisotropic Band)**

  • Appears **dark** in color
  • Contains both **thick (myosin)** and **thin (actin) filaments**
  • Middle region of thick filaments held together by **M-line** (M-disc)
  • During muscle contraction, A-band length **remains constant**
  • **H-Zone**

  • Region within A-band containing only thick filaments
  • Located between edges of overlapping thin filaments
  • In resting state, central part of thick filaments is not overlapped
  • Decreases during contraction as thin filaments slide over thick filaments
  • **Z-Line (Z-Disc)**

  • Elastic protein structure
  • Bisects each I-band
  • Thin filaments attached to Z-lines on both sides
  • Z-lines move toward each other during contraction
  • **Sarcomere**: Region between two Z-lines; this is the **contractile unit**

    Sarcoplasmic Reticulum and Calcium Storage

  • **Sarcoplasmic reticulum**: Specialized smooth endoplasmic reticulum in muscle fibers
  • Functions as the **main calcium ion (Ca²⁺) store** in muscle cells
  • Calcium is essential for initiating muscle contraction
  • Calcium release is triggered by action potential spreading through T-tubules
  • **T-tubules**: Invaginations of sarcolemma that penetrate deep into muscle fiber
  • ---

    STRUCTURE OF CONTRACTILE PROTEINS

    Actin (Thin Filaments)

    **Composition**:

  • Two **F-actin** (filamentous actin) molecules wound helically around each other
  • Each F-actin is a polymer of monomeric **G-actin** (globular actin) subunits
  • Diameter: approximately 7 nm
  • **Associated Proteins**:

  • **Tropomyosin**: Two protein molecules run along the length of F-actin
  • Thin rod-like structure
  • Covers the myosin-binding sites on actin in resting state
  • **Troponin**: Complex regulatory protein
  • Distributed at regular intervals (approximately every 40 nm) on tropomyosin
  • Three subunits:
  • **TnC (Troponin C)**: Binds calcium ions
  • **TnI (Troponin I)**: Inhibitory subunit; masks binding site
  • **TnT (Troponin T)**: Binds to tropomyosin
  • In resting state: TnI subunit masks active binding sites for myosin on actin
  • **Function of Actin**:

  • Provides binding sites for myosin heads
  • Forms cross-bridges with myosin during contraction
  • Thin appearance compared to myosin filaments
  • Myosin (Thick Filaments)

    **Basic Unit: Meromyosin**

  • Monomeric protein unit making up thick filaments
  • Approximately 110 nm in length
  • Two distinct regions:
  • **1. Heavy Meromyosin (HMM)**

  • Comprises approximately 50% of meromyosin
  • **Globular head**:
  • Spherical structure projecting outward
  • Acts as **active ATPase enzyme**
  • Has two critical sites:
  • **ATP-binding site**: Binds ATP molecules for energy
  • **Actin-binding site** (active site): Binds to exposed sites on actin filaments
  • Projects outward at regular intervals and angles from filament surface
  • **Short arm**: Connects head to tail; provides flexibility for power stroke
  • **2. Light Meromyosin (LMM)**

  • Forms the rod-like tail
  • Structural protein
  • Anchors myosin monomers together to form thick filament
  • **Thick Filament Structure**:

  • Formed by polymerization of hundreds of meromyosin molecules
  • Myosin heads project outward at angles (approximately 65° to 70°)
  • Two myosin head clusters at each end oriented in opposite directions
  • Provides bipolarity to thick filament
  • Diameter: approximately 15 nm
  • **Functions of Myosin**:

  • Catalyzes ATP hydrolysis to provide energy for contraction
  • Forms cross-bridges with actin
  • Causes sliding of thin filaments
  • ---

    MECHANISM OF MUSCLE CONTRACTION

    Sliding Filament Theory

    **Definition**: **Muscle contraction is brought about by the sliding of thin filaments over the thick filaments without the filaments themselves changing length.**

    Proposed by: H.E. Huxley and others (1950s)

    **Key Evidence**:

  • During contraction, I-bands shorten but A-bands remain the same length
  • Sarcomere length decreases as Z-lines move closer
  • Thin and thick filaments overlap more
  • Step-by-Step Mechanism of Contraction

    #### Step 1: Neural Signal and Neuromuscular Junction

    **Motor Unit**: One motor neuron + all muscle fibers it innervates

    **Neuromuscular Junction (Motor End Plate)**:

  • Point of contact between axon terminal of motor neuron and sarcolemma
  • Presynaptic membrane: Axon terminal
  • Synaptic cleft: 50 nm gap
  • Postsynaptic membrane: Sarcolemma with receptors
  • **Process**:

  • Action potential travels along motor neuron axon
  • Reaches axon terminal
  • Triggers release of neurotransmitter
  • #### Step 2: Neurotransmitter Release

    **Neurotransmitter**: **Acetylcholine (ACh)**

  • Released from synaptic vesicles in axon terminal
  • Diffuses across synaptic cleft (50 nm)
  • Binds to **acetylcholine receptors** on sarcolemma
  • These are ligand-gated ion channels
  • #### Step 3: Generation of Action Potential

  • ACh binding causes conformational change in receptors
  • Sodium (Na⁺) ions enter the muscle fiber
  • **Depolarization** of sarcolemma
  • Action potential is generated
  • Action potential spreads across entire sarcolemma and down T-tubules
  • #### Step 4: Calcium Ion Release

    **Location**: Sarcoplasmic reticulum (calcium store)

    **Process**:

  • Action potential travels down T-tubules
  • Triggers opening of voltage-sensitive calcium channels in sarcoplasmic reticulum
  • **Calcium ions (Ca²⁺) flood into sarcoplasm**
  • Increase in intracellular Ca²⁺ concentration (from ~0.1 μM to ~1-10 μM)
  • #### Step 5: Removal of Inhibition

    **Initial state (resting muscle)**:

  • TnI subunit of troponin masks the myosin-binding site on actin
  • Tropomyosin blocks access to binding site
  • **Upon Ca²⁺ binding**:

  • Ca²⁺ binds to **TnC (Troponin C)** subunit
  • Conformational change in troponin complex
  • Troponin moves, pulling tropomyosin aside
  • **Myosin-binding sites on actin become exposed**
  • #### Step 6: Cross-Bridge Formation

    **Process**:

  • Myosin heads, already activated by ATP hydrolysis (containing ADP + Pi), attach to exposed binding sites on actin
  • Forms **cross-bridge** between thick and thin filaments
  • Myosin head is in high-energy state
  • Power stroke is about to occur
  • #### Step 7: Power Stroke (Ratcheting)

    **Process**:

  • Myosin head pivots on its short arm
  • Pulls actin filament toward center of A-band
  • Z-lines attached to actin move inward
  • **Sarcomere shortens** (approximately 10 nm movement per power stroke)
  • ADP and Pi are released from myosin head
  • Myosin head moves to low-energy state
  • **Effects**:

  • **I-bands decrease in length** (thin filaments slide over thick filaments)
  • **A-bands remain constant** in length
  • **H-zone decreases** (thin filaments extend further)
  • #### Step 8: Cross-Bridge Breaking (Rigor State)

    **Trigger**: New ATP molecule binds to myosin head

    **Process**:

  • ATP binding causes conformational change
  • Myosin head releases from actin (cross-bridge breaks)
  • Muscle fiber enters **rigor state** (maximum force) if no ATP available
  • **Significance**: This is why muscles become rigid after death (**rigor mortis**) when ATP production stops

    #### Step 9: ATP Hydrolysis and Re-activation

    **Process**:

  • ATPase activity of myosin head hydrolyzes ATP
  • ATP → ADP + Pi + Energy
  • Energy is stored in myosin head
  • Myosin head returns to high-energy conformation
  • Myosin head moves back to original position (without binding to actin) ready for next power stroke
  • #### Step 10: Relaxation

    **Trigger**: Calcium ions are pumped back to sarcoplasmic reticulum

    **Process**:

  • Neural signal stops
  • Acetylcholine release stops
  • Ca²⁺ levels in sarcoplasm decrease
  • Ca²⁺ is removed from TnC
  • Tropomyosin returns to blocking position
  • Myosin-binding sites on actin are masked again
  • Myosin heads cannot bind
  • Z-lines return to original position
  • **Muscle relaxes**
  • **Energy requirement**: ATP needed for muscle relaxation to pump Ca²⁺ (via Ca²⁺-ATPase pumps)

    Muscle Contraction Cycle Summary

    **In rapidly contracting muscle**:

  • Cross-bridge formation, power stroke, and cross-bridge breaking occur continuously
  • Multiple myosin heads engage sequentially
  • One myosin head completes cycle while others are binding or generating power strokes
  • Sliding continues until Ca²⁺ is removed
  • **Number of cross-bridges**:

  • Only about 50% of myosin heads engaged at any given moment in active contraction
  • Rotation of myosin heads can drag actin filaments several micrometers
  • ---

    MUSCLE FIBER TYPES

    Red Fibers (Slow-Twitch, Type I Fibers)

    **Appearance**: Reddish color

    **Pigment**: High content of **myoglobin**

  • Oxygen-binding pigment
  • Similar structure to hemoglobin
  • Stores oxygen for prolonged use
  • **Mitochondrial Content**: Abundant mitochondria

    **Metabolic Pathway**: **Aerobic respiration** (use oxygen)

  • Produce ATP efficiently
  • Can sustain contraction for long periods
  • **Energy Source**: Oxidative phosphorylation

  • Break down glucose and fatty acids with oxygen
  • **Contraction Speed**: Slow (slow-twitch)

    **Fatigue Resistance**: Very resistant to fatigue

    **Function**: Postural muscles, endurance activities (long-distance running, holding posture)

    **Location**: Postural muscles of neck and back

    **ATPase Activity**: Low

    White Fibers (Fast-Twitch, Type II Fibers)

    **Appearance**: Pale or whitish color

    **Pigment**: Very low myoglobin content

    **Mitochondrial Content**: Few mitochondria

    **Sarcoplasmic Reticulum**: High amount (stores calcium)

    **Metabolic Pathway**: **Anaerobic respiration** (without oxygen)

  • Depend on glycolysis
  • Rapid but less efficient ATP production
  • Produce lactic acid as byproduct
  • **Energy Source**:

  • Breakdown of glycogen and glucose
  • Creatine phosphate (quick energy source)
  • **Contraction Speed**: Fast (fast-twitch)

    **Contraction Force**: Generate high force initially

    **Fatigue**: Fatigue quickly due to lactic acid accumulation

    **Function**: Rapid, powerful movements (sprinting, jumping, weight lifting)

    **Location**: Limb muscles involved in movement

    **ATPase Activity**: High

    Muscle Fatigue

    **Definition**: Decreased ability of muscle to maintain force of contraction

    **Causes**:

    1. **Accumulation of lactic acid**: Anaerobic metabolism produces lactate ions that lower pH

    2. **Depletion of glycogen stores**: Reduced substrate for ATP production

    3. **Accumulation of Pi (inorganic phosphate)**: Inhibits cross-bridge formation and power stroke

    4. **Reduced Ca²⁺ release**: Sarcoplasmic reticulum Ca²⁺ stores become depleted

    5. **Central nervous fatigue**: Reduced neural drive

    6. **Accumulation of K⁺ outside cells**: Affects action potential generation

    **Recovery**: Lactic acid is metabolized, oxygen is supplied, energy stores are replenished

    ---

    SKELETAL SYSTEM

    Overview

    **Definition**: The skeletal system is a framework of bones and cartilages that supports the body and enables movement.

    **Composition in humans**:

  • **206 bones** (in adults; newborns have ~270, many fuse during development)
  • **Cartilages**: Smaller number in specific locations
  • **Components**: Bone and cartilage are specialized connective tissues

    Bone vs. Cartilage

    | Feature | Bone | Cartilage |

    |---------|------|-----------|

    | Matrix | Hard, rigid | Slightly pliable (flexible) |

    | Mineral composition | Rich in calcium salts | Contains chondroitin salts |

    | Rigidity | Very hard and strong | Flexible and slightly compressible |

    | Vascularity | Well-vascularized | Avascular (no blood vessels) |

    | Function | Support, protection, movement | Reduces friction, provides support |

    **Chondroitin salts**: Provide elasticity and flexibility to cartilage

    Divisions of Skeletal System

    #### A. AXIAL SKELETON

    **Definition**: Bones distributed along the main axis of the body

    **Total bones**: 80 bones

    **Components**:

    1. **Skull**

    2. **Vertebral column**

    3. **Sternum**

    4. **Ribs**

    ##### 1. SKULL

    **Total bones**: 22 bones + 3 ear ossicles

    **Composition**:

  • **Cranial bones**: 8 bones forming cranium
  • Frontal bone (1): Forms forehead
  • Parietal bones (2): Sides and roof of cranium
  • Temporal bones (2): Sides of cranium; contain ear canal
  • Occipital bone (1): Back and base of cranium; contains foramen magnum (opening for spinal cord)
  • Sphenoid bone (1): Forms base of cranium; contains pituitary gland fossa
  • Ethmoid bone (1): Between eye sockets; forms part of nasal septum
  • **Facial bones**: 14 bones forming front of skull
  • Maxilla (2): Upper jaw; fused to form single structure
  • Mandible (1): Lower jaw; single bone
  • Nasal bones (2): Form nose bridge
  • Lacrimal bones (2): Inner corners of eye sockets; contain lacrimal glands
  • Zygomatic bones (2): Cheekbones
  • Vomer (1): Nasal septum
  • Palatine bones (2): Roof of mouth
  • Inferior nasal conchae (2): Nasal passages
  • **Special Bones**:

  • **Hyoid bone**: U-shaped bone at base of buccal cavity; only unpaired facial bone
  • **Ear Ossicles**: Three tiny bones in each middle ear (6 total)

  • **Malleus** (hammer): Connected to tympanum
  • **Incus** (anvil): Middle position
  • **Stapes** (stirrup): Connected to inner ear
  • Function: Transmit vibrations from eardrum to inner ear
  • **Articulation with Vertebral Column**:

  • Skull articulates with first vertebra (atlas) via **occipital condyles**
  • **Two occipital condyles**: Makes human skull dicondylic (two points of articulation)
  • Allows forward and backward nodding movements
  • ##### 2. VERTEBRAL COLUMN

    **Definition**: Series of serially arranged bones (vertebrae) forming the backbone

    **Position**: Dorsally placed (along the back)

    **Total vertebrae**: 26 in adults (some are fused)

    **Extension**: From base of skull to end of vertebral column

    **Functions**:

  • Protects spinal cord (which runs through neural canal)
  • Supports head
  • Provides attachment points for ribs and back musculature
  • Provides structure to trunk
  • Allows movement of trunk
  • **Regions** (from skull downward):

    1. **Cervical vertebrae**: 7

  • Smallest vertebrae
  • Located in neck region
  • **Atlas (C1)**: First cervical vertebra; articulates with occipital condyles
  • **Axis (C2)**: Second cervical vertebra; contains dens (odontoid process) for rotation
  • **Interesting fact**: All mammals (including giraffes and humans) have 7 cervical vertebrae
  • Allow head rotation and movement
  • 2. **Thoracic vertebrae**: 12

  • Located in chest region
  • Articulate with ribs
  • Have facets for rib articulation
  • Heart and lungs lie at level of thoracic vertebrae
  • 3. **Lumbar vertebrae**: 5

  • Located in lower back region
  • Largest vertebrae (bear more weight)
  • Support most body weight
  • 4. **Sacral vertebrae**: 5 (fused into one **sacrum**)

  • Fused together in adults
  • Forms triangular bone
  • Forms part of pelvic girdle
  • Articulates with coccyx below
  • 5. **Coccygeal vertebrae**: 4 (fused into one **coccyx**)

  • Tail bone in humans
  • Vestigial structure (no functional tail in humans)
  • Reduced size
  • **Intervertebral Discs**:

  • Fibrocartilage structure between adjacent vertebrae
  • Contain **nucleus pulposus** (gel-like center)
  • Absorb shock and allow limited movement
  • Can herniate if damaged ("slipped disc")
  • **Typical Vertebra Structure**:

  • **Vertebral body**: Main load-bearing part
  • **Vertebral arch**: Forms neural canal (spinal cord passage)
  • **Neural canal**: Central hollow region; passage for spinal cord
  • **Spinous process**: Posterior projection (felt along spine)
  • **Transverse processes**: Lateral projections
  • **Facets**: Articulating surfaces with adjacent vertebrae
  • ##### 3. STERNUM (Breastbone)

    **Description**: Flat bone on ventral midline of thorax

    **Position**: Front and center of rib cage

    **Function**: Articulation point for ribs; protection of heart and lungs

    **Divisions**: Three parts

  • **Manubrium**: Upper part
  • **Body**: Middle part
  • **Xiphoid process**: Lower part (may become ossified)
  • ##### 4. RIBS

    **Total**: 12 pairs (24 ribs)

    **Attachment**:

  • **Dorsally**: Connected to thoracic vertebrae
  • **Ventrally**: Connected to sternum (directly or indirectly)
  • **Structure**:

  • Thin, flat bones
  • Have two articulation surfaces on dorsal end
  • Called **bicephalic ribs** (two-headed)
  • **Classification**:

    1. **True ribs (Vertebrosternal ribs)**: 1st-7th pairs (7 pairs)

  • Articulate directly with sternum via hyaline cartilage
  • Fully connect thoracic vertebrae to sternum
  • 2. **False ribs (Vertebrochondral ribs)**: 8th-10th pairs (3 pairs)

  • Do NOT articulate directly with sternum
  • Connect to 7th rib via hyaline cartilage
  • Indirectly attach to sternum
  • 3. **Floating ribs**: 11th-12th pairs (2 pairs)

  • No ventral attachment to sternum
  • Only attached to thoracic vertebrae dorsally
  • Free anteriorly
  • **Rib Cage**:

  • Structure formed by: Thoracic vertebrae + ribs + sternum + costal cartilages
  • Function: Protects heart, lungs, and other thoracic organs
  • Involved in respiration (movement allows breathing)
  • #### B. APPENDICULAR SKELETON

    **Definition**: Bones of limbs and their girdles

    **Total bones**: 126 bones (4 limbs + 2 girdles)

    **Components**:

    1. Pectoral girdle (shoulder girdle) + upper limbs

    2. Pelvic girdle + lower limbs

    ##### PECTORAL GIRDLE (Shoulder Girdle)

    **Function**: Articulates upper limbs with axial skeleton

    **Bones**: Two halves, each containing 2 bones

    **Per side**:

    1. **Clavicle** (collar bone)

  • Long, slender bone with two curvatures
  • Articulates with scapula laterally and sternum medially
  • Readily breaks due to its position and structure
  • Provides attachment for muscles
  • 2. **Scapula** (shoulder blade)

  • Large, triangular flat bone
  • Located dorsally on thorax
  • Between 2nd and 7th ribs
  • Has three borders: superior, lateral, medial
  • Spine: Ridge on posterior surface
  • **Acromion**: Flat, expanded process at apex of spine
  • **Clavicle articulates with acromion**
  • **Glenoid cavity**: Cup-shaped depression on lateral surface
  • **Head of humerus articulates with glenoid cavity** forming shoulder joint
  • **Coracoid process**: Beak-like projection; attachment for muscles and ligaments
  • ##### UPPER LIMB BONES (Forelimb)

    **Each upper limb**: 30 bones

    **Regions** (from shoulder to fingertips):

    1. **Humerus** (upper arm bone)

  • Long bone (largest bone of upper limb)
  • Has spherical head that articulates with glenoid cavity
  • **Deltoid tuberosity**: Rough area for muscle attachment
  • Articulates with radius and ulna at elbow
  • 2. **Radius** (lateral forearm bone, thumb side)

  • Shorter than ulna
  • Has disc-shaped head articulating with humerus
  • **Radial tuberosity**: Attachment for biceps muscle
  • Allows rotation (supination and pronation)
  • 3. **Ulna** (medial forearm bone, pinky side)

  • Longer than radius
  • **Olecranon process**: Posterior projection forming elbow prominence
  • **Coronoid process**: Anterior projection
  • Forms hinge joint with humerus
  • Articulates with radius
  • 4. **Carpals** (wrist bones)

  • 8 small bones arranged in two rows
  • Provide flexibility to wrist
  • Named: Scaphoid, Lunate, Triquetrum, Pisiform (proximal row); Trapezium, Trapezoid, Capitate, Hamate (distal row)
  • Allow wrist flexion, extension, and rotation
  • 5. **Metacarpals** (palm bones)

  • 5 elongated bones
  • Numbered 1-5 from thumb to pinky
  • Form structure of palm
  • Articulate with carpals and phalanges
  • 6. **Phalanges** (fingers/digits bones)

  • 14 bones total
  • **Thumb**: 2 phalanges (proximal, distal)
  • **Each finger**: 3 phalanges (proximal, middle, distal)
  • Smallest bones of upper limb
  • ##### PELVIC GIRDLE

    **Function**: Articulates lower limbs with axial skeleton; provides support

    **Structure**: Two halves meeting ventrally

    **Bones per side**: Each coxal bone formed by fusion of three bones

    **Components of each coxal bone**:

    1. **Ilium** (upper and largest)

  • Forms wing-like structure
  • Iliac crest: Upper border; palpable (can be felt)
  • **Acetabulum**: Deep cup-shaped cavity formed by fusion point of three bones
  • **Femoral head articulates with acetabulum**
  • 2. **Ischium** (lower and posterior)

  • Forms lower and back part of pelvis
  • **Ischial tuberosities**: Points on which we sit
  • **Ischial spine**: Projection pointing inward
  • 3. **Pubis** (anterior and medial)

  • Forms pubic bone anteriorly
  • **Pubic symphysis**: Cartilaginous joint between two pubic bones ventrally
  • Contains fibrous cartilage providing limited movement
  • Widens during pregnancy to facilitate childbirth
  • **Acetabulum**:

  • Deep socket where femur articulates
  • Formed by fusion of ilium, ischium, and pubis
  • Provides stable articulation for hip joint
  • Deeper and more enclosed than glenoid cavity
  • **Pelvic Structure and Sexual Dimorphism**:

  • **Female pelvis**: Wider, larger pelvic inlet, wider subpubic angle (facilitates childbirth)
  • **Male pelvis**: Narrower, deeper, smaller pelvic inlet
  • ##### LOWER LIMB BONES (Hind limb)

    **Each lower limb**: 30 bones

    **Regions** (from hip to toes):

    1. **Femur** (thigh bone)

  • **Longest and strongest bone**
  • MCQs — 10 Questions with Answers

    Q1. Which of the following is a characteristic feature of smooth muscles?

    • A. They are striated and voluntary in nature
    • B. They are non-striated and involuntary in nature ✓
    • C. They are striated and involuntary in nature
    • D. They lack sarcolemma and sarcoplasm

    Answer: B — Smooth muscles are found in visceral organs, lack striations, and are controlled by the autonomic nervous system, making them involuntary.

    Q2. The functional unit of muscle contraction is the sarcomere, which is defined as the region between:

    • A. Two successive M lines
    • B. Two successive I bands
    • C. Two successive Z lines ✓
    • D. Two successive H zones

    Answer: C — A sarcomere is precisely the portion of myofibril bounded by two consecutive Z lines, representing one complete contraction unit.

    Q3. Amoeboid movement in white blood cells is primarily facilitated by:

    • A. Contraction of myosin filaments
    • B. Beating of flagella
    • C. Formation of pseudopodia and protoplasmic streaming ✓
    • D. Coordinated ciliary action

    Answer: C — Amoeboid movement involves temporary projections (pseudopodia) formed by cytoplasmic streaming, similar to movement in Amoeba protozoans.

    Q4. In a relaxed muscle fibre, the H zone represents:

    • A. The entire A band
    • B. The central region of the A band not covered by thin filaments ✓
    • C. The entire I band
    • D. The region between tropomyosin and troponin

    Answer: B — The H zone is the uncovered central portion of thick filaments in the resting state; it disappears as thin filaments slide during contraction.

    Q5. Which statement about troponin is correct? (A) Troponin is located on thick filaments (B) Troponin masks myosin-binding sites on actin at rest

    • A. Both A and B are correct
    • B. Only A is correct
    • C. Only B is correct ✓
    • D. Neither A nor B is correct

    Answer: C — Troponin is located on tropomyosin (which lies on thin actin filaments, not thick filaments), and it masks myosin-binding sites until calcium binds.

    Q6. Which of the following is NOT a correct characteristic of cardiac muscles?

    • A. They are striated in appearance
    • B. They are involuntary and controlled by the somatic nervous system ✓
    • C. They form branching networks in the heart
    • D. They possess intrinsic rhythmicity

    Answer: B — Cardiac muscles are involuntary but controlled by the autonomic nervous system and intrinsic pacemakers, not the somatic nervous system.

    Q7. Ciliary movement in the trachea helps in:

    • A. Locomotion of the organism
    • B. Removal of dust particles and foreign substances ✓
    • C. Contraction of respiratory muscles
    • D. Production of mucus in the lungs

    Answer: B — Coordinated ciliary beating in tracheal epithelium removes inhaled dust and foreign particles, protecting the respiratory system.

    Q8. If a muscle fibre at rest has an H zone of 1.0 μm, and during maximum contraction the H zone disappears, this indicates: (A) Thin filaments have slid over thick filaments (B) Z lines have moved closer to each other

    • A. Both A and B are correct ✓
    • B. Only A is correct
    • C. Only B is correct
    • D. Neither A nor B is correct

    Answer: A — During contraction, thin filaments slide over thick filaments (reducing H zone), and Z lines move closer, both occurring simultaneously in the sliding filament mechanism.

    Q9. The sarcoplasmic reticulum in muscle fibres is specialised for:

    • A. Synthesis of contractile proteins
    • B. Storage and release of calcium ions ✓
    • C. Formation of myofilaments
    • D. Attachment of muscle to skeleton

    Answer: B — Sarcoplasmic reticulum is the muscle-cell version of endoplasmic reticulum that stores Ca²⁺ ions essential for triggering muscle contraction.

    Q10. A student observed that locomotion requires coordinated activity of three systems. Which of the following correctly identifies all three? (A) Muscular, skeletal, and neural systems (B) Muscular, digestive, and nervous systems (C) Skeletal, circulatory, and nervous systems (D) Muscular, endocrine, and skeletal systems

    • A. Only A is correct ✓
    • B. Only B is correct
    • C. Only C is correct
    • D. A, B, and C are all correct

    Answer: A — Locomotion requires perfect coordination among muscles (contraction), skeleton (leverage), and neural system (command and control)—not digestive, circulatory, or endocrine systems.

    Flashcards

    What is the difference between movement and locomotion?

    Movement is any change in body position, while locomotion is movement that results in change of place or location; all locomotions are movements but not all movements are locomotions.

    Name the three types of movements exhibited by human cells.

    Amoeboid movement (macrophages), ciliary movement (tracheal epithelium), and muscular movement (skeletal muscles).

    What is the sarcomere?

    The sarcomere is the functional unit of muscle contraction, defined as the portion of myofibril between two successive Z lines.

    Distinguish between striated and smooth muscles.

    Striated muscles (skeletal and cardiac) have alternating dark and light bands due to actin-myosin arrangement; smooth muscles (visceral) lack striations and appear uniform under microscope.

    What are the two main contractile proteins in muscle fibres?

    Actin (thin filaments) and myosin (thick filaments) are the main contractile proteins arranged parallel to each other in the myofibril.

    What is the role of troponin in muscle contraction?

    In the resting state, troponin masks the active binding sites for myosin on actin filaments, preventing contraction until calcium binds to troponin.

    Define the H zone in a sarcomere.

    The H zone is the central part of the thick filament not overlapped by thin filaments in a relaxed muscle fibre.

    What is sarcolemma?

    Sarcolemma is the plasma membrane that encloses each muscle fibre and contains the sarcoplasm.

    Why are cardiac muscles called involuntary muscles?

    Cardiac muscles are involuntary because their contractions are not directly controlled by voluntary (somatic) nervous system but by the autonomic nervous system and intrinsic pacemakers.

    What is sarcoplasmic reticulum?

    Sarcoplasmic reticulum is the endoplasmic reticulum in muscle fibres that acts as the storage house for calcium ions necessary for contraction.

    Important Board Questions

    Define locomotion and distinguish it from general movement. Give one example of each. [2 marks]

    Locomotion = change of place; movement = change in body position. Example: walking is locomotion; blinking is movement only. Use definition-based language.

    Explain the structure of a sarcomere with reference to the arrangement of actin, myosin, and regulatory proteins. How does this arrangement enable muscle contraction? [5 marks]

    Describe Z line, I band (actin + tropomyosin + troponin), A band (myosin), H zone. Explain sliding: troponin releases at Ca²⁺ signal → myosin heads bind → thin filaments slide over thick filaments → Z lines approach = shortening.

    Compare and contrast the three types of muscles found in the human body with respect to their location, structure, regulation, and functional significance in locomotion and internal organ movements. [6 marks]

    Create comparison table: skeletal (striated, voluntary, limbs, locomotion) vs. visceral (smooth, involuntary, gut/uterus, transport) vs. cardiac (striated, involuntary, heart, pumping). Link each to nervous system control and role in coordinated movement.

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