Locomotion and Movement Class 11 Notes | CBSE Biology Chapter 17

Chapter summary

Locomotion and Movement covers how the human body moves, from the three cellular movements (amoeboid, ciliary and muscular) to the skeletal muscle and the 206-bone skeleton that produce locomotion. It explains muscle structure down to the sarcomere, the sliding filament theory of contraction, the types of joints, and high-yield disorders. It is a frequently tested NEET chapter that blends physiology with anatomy, so it reliably contributes one or two questions every year.

Chapter notes

Table of Contents


Key Concepts

1. Movement and Locomotion

Watch your eyelid blink or your heart beat - that is movement, a change in position of a body part. When you walk to school, your whole body changes place - that is locomotion.

Movement is a characteristic feature of all living organisms; it may or may not change the position of the whole body. Locomotion is the voluntary movement of an organism from one place to another. All locomotion is movement, but not all movement is locomotion.

Key idea: Animals move for food, shelter, a mate, breeding, a suitable climate, or to escape predators.


2. Types of Movement

Cells of the human body show three main types of movement.

  • Amoeboid movement: shown by macrophages and leucocytes (WBCs). It occurs by the streaming of cytoplasm to form pseudopodia, involving the cytoskeleton (microfilaments).
  • Ciliary movement: occurs in internal tubular organs lined by ciliated epithelium - the trachea (moves dust-trapped mucus), and the female reproductive tract (moves the ovum/egg through the oviduct).
  • Muscular movement: movement of limbs, jaws, tongue, etc. needs the contraction of muscle. Most locomotion in higher animals depends on it.

3. Muscle - Properties and Types

Muscle is a specialised contractile tissue of mesodermal origin, making up 40–50% of an adult human’s body weight. Its key properties are excitability, contractility, extensibility, and elasticity.

Three Types of Muscle

TypeLocationStriationsControl / Nuclei
Skeletal (striated)Attached to bonesStriatedVoluntary; multinucleate
Smooth (visceral)Inner walls of hollow organs (gut, blood vessels)Non-striatedInvoluntary; uninucleate, spindle-shaped
CardiacHeart wallStriatedInvoluntary; uninucleate, branched, with intercalated discs

4. Structure of Skeletal Muscle

A skeletal muscle is built like a bundle of bundles. Each muscle is made of many parallel muscle fibres (myofibres) grouped into bundles called fascicles, held together by connective tissue (fascia).

Each muscle fibre is a long, cylindrical, multinucleate cell. Its plasma membrane is the sarcolemma, the cytoplasm is the sarcoplasm, and the endoplasmic reticulum is the sarcoplasmic reticulum (SR) - the store of calcium ions.

[DIAGRAM: Muscle → fascicle → muscle fibre → myofibril → sarcomere, showing A-band, I-band, H-zone, Z-line and M-line.]

The sarcoplasm contains many parallel myofibrils, each showing alternating dark and light bands - the source of the striations.

  • A-band (dark): contains thick myosin filaments (with overlapping actin). Anisotropic.
  • I-band (light): contains only thin actin filaments. Isotropic.
  • Z-line: bisects each I-band; the thin filaments are anchored to it.
  • H-zone: the central part of the A-band with only myosin (no overlap).
  • M-line: holds the myosin filaments together at the centre of the H-zone.

The portion between two successive Z-lines is the sarcomere - the functional (contractile) unit of a muscle.


5. Thick and Thin Filaments

The two contractile proteins are arranged as overlapping filaments.

  • Thin filament (actin): two F-actin strands helically wound; each F-actin is a polymer of G-actin monomers. Two filaments of tropomyosin run alongside, and a complex protein troponin sits at regular intervals over tropomyosin, masking the active (myosin-binding) sites in a resting muscle.
  • Thick filament (myosin): a polymer of many meromyosin molecules. Each meromyosin has a globular head with a short arm (HMM) projecting outward - this head is the cross-bridge and carries ATPase activity and binding sites for ATP and actin - and a tail (LMM).

6. Sliding Filament Theory of Muscle Contraction

Proposed by H. E. Huxley and A. F. Huxley, the sliding filament theory states that muscle contraction occurs because the thin (actin) filaments slide over the thick (myosin) filaments - the filaments themselves do not shorten.

Steps of Contraction

  • A signal from the CNS reaches the neuromuscular junction (motor end plate), releasing the neurotransmitter acetylcholine.
  • This generates an action potential in the sarcolemma, causing the sarcoplasmic reticulum to release Ca²⁺ into the sarcoplasm.
  • Ca²⁺ binds to troponin on actin, shifting tropomyosin and exposing the active sites.
  • Myosin heads bind to the exposed actin sites, forming cross-bridges, and pull the thin filaments inward (the power stroke) - ATP is hydrolysed by myosin ATPase.
  • The Z-lines are pulled closer, so the sarcomere and I-band shorten while the A-band stays constant length; the H-zone shrinks.
  • Fresh ATP binds the myosin head, breaking the cross-bridge; the head returns and the cycle repeats. When Ca²⁺ is pumped back into the SR, the active sites are masked again and the muscle relaxes.

Key idea (NEET favourite): During contraction the A-band length is unchanged; only the I-band and H-zone get shorter.


7. Red and White Muscle Fibres

Skeletal muscle fibres are of two types based on the amount of the red pigment myoglobin.

FeatureRed fibres (Type I)White fibres (Type II)
MyoglobinHigh (red colour)Low (pale)
MitochondriaNumerousFew
Sarcoplasmic reticulumLessAbundant
RespirationAerobicAnaerobic
ContractionSlow, sustained (do not fatigue easily)Fast, fatigue quickly

Note: Red fibres are suited for posture and endurance; white fibres for quick, powerful bursts.


8. The Skeletal System

The skeletal system is the framework of bones and a few cartilages that supports the body, protects organs, and provides surfaces for muscle attachment. Bone has a hard matrix rich in calcium salts; cartilage has a slightly pliable matrix (chondroitin salts).

The adult human skeleton has 206 bones, divided into the axial and the appendicular skeleton.


9. Axial Skeleton (80 bones)

The axial skeleton forms the main axis of the body - skull, vertebral column, ribs, and sternum.

  • Skull (29 bones): 8 cranial + 14 facial bones, 6 ear ossicles (3 in each middle ear - malleus, incus, stapes), and 1 hyoid. A single U-shaped hyoid bone lies at the base of the buccal cavity.
  • Vertebral column (26 bones): 7 cervical, 12 thoracic, 5 lumbar, 1 sacrum (fused), 1 coccyx (fused). The first vertebra is the atlas, which articulates with the occipital condyles of the skull.
  • Ribs (24 / 12 pairs): 7 pairs true (vertebrosternal), 3 pairs false (vertebrochondral), 2 pairs floating (vertebral) ribs. Each rib is a thin flat bone connecting the vertebral column and the sternum.
  • Sternum (1): a flat bone on the ventral midline of the thorax. Ribs + sternum + thoracic vertebrae form the rib cage.

10. Appendicular Skeleton (126 bones)

The appendicular skeleton consists of the bones of the limbs and the two girdles.

  • Forelimb (30 bones each): humerus, radius and ulna, 8 carpals, 5 metacarpals, 14 phalanges.
  • Hindlimb (30 bones each): femur (the longest bone), tibia and fibula, patella (kneecap), 7 tarsals, 5 metatarsals, 14 phalanges.
  • Pectoral girdle: each half has a clavicle (collar bone) and a scapula (shoulder blade). The scapula bears a socket - the glenoid cavity - for the humerus.
  • Pelvic girdle: two coxal (hip) bones, each formed by the fusion of ilium, ischium, and pubis. The socket - the acetabulum - receives the head of the femur.

11. Joints

A joint (articulation) is the point of contact between two or more bones, or between bone and cartilage. Joints are essential for all movement and locomotion. They are classified by their degree of mobility.

Type of jointMobilityExample
Fibrous (fixed)ImmovableSutures of the skull
CartilaginousSlightly movableJoints between adjacent vertebrae
SynovialFreely movable (synovial fluid in the cavity)See below

Types of Synovial Joints

  • Ball and socket: shoulder and hip - movement in all planes.
  • Hinge: knee, elbow - movement in one plane.
  • Pivot: between the atlas and axis - rotation.
  • Gliding: between carpals (wrist).
  • Saddle: between the carpal and metacarpal of the thumb.

12. Disorders of the Muscular and Skeletal System

A few named disorders are almost guaranteed in NEET and boards - learn the one-line cause for each.

DisorderCause / Key Feature
Myasthenia gravisAuto-immune disorder affecting the neuromuscular junction → fatigue, weakness and paralysis of skeletal muscle.
Muscular dystrophyGenetic disorder → progressive degeneration of skeletal muscle.
TetanyRapid spasms (wild contractions) of muscle due to low Ca²⁺ in body fluid.
ArthritisInflammation of joints.
OsteoporosisAge-related disorder; decreased bone mass and higher fracture risk, commonly due to lowered oestrogen levels.
GoutInflammation of joints due to accumulation of uric acid crystals.

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Weightage in Board & Entrance Exams

ExamTypical WeightageMost-Tested Areas
CBSE Board (Class 11)4–6 marksSliding filament theory, muscle structure, joints, disorders
NEET1–2 questions almost every yearSarcomere bands, contraction mechanism, bone count, red vs white fibres

[TABLE: Question-type split - VSA (1 mark): definitions, examples of movement, disorder causes; SA (2–3 marks): muscle ultrastructure, red vs white fibres, joint types; LA (5 marks): sliding filament theory, axial vs appendicular skeleton.]


Important Definitions

TermDefinition
MovementA change in the position of a body part; need not move the whole body.
LocomotionVoluntary movement of an organism from one place to another.
SarcomereThe portion of a myofibril between two successive Z-lines; the functional unit of contraction.
Sarcoplasmic reticulumThe endoplasmic reticulum of a muscle fibre; stores and releases Ca²⁺.
Sliding filament theoryContraction occurs by thin filaments sliding over thick filaments.
Cross-bridgeThe myosin head that binds actin and pulls it during contraction.
Joint / articulationPoint of contact between bones (or bone and cartilage) enabling movement.
TetanyRapid muscle spasms caused by low Ca²⁺ in body fluid.
OsteoporosisAge-related fall in bone mass; raises fracture risk (low oestrogen).
GoutJoint inflammation due to deposition of uric acid crystals.

Solved Examples & NEET Facts

Example 1

During muscle contraction, which bands of the sarcomere change in length and how?

Answer: The I-band and H-zone shorten and the sarcomere length decreases. The A-band length stays unchanged because the myosin filaments do not shorten - the actin filaments merely slide inward.

Example 2

Name the protein to which Ca²⁺ binds during contraction and state its effect.

Answer: Ca²⁺ binds to troponin on the thin filament. This shifts tropomyosin and exposes the myosin-binding (active) sites on actin, allowing cross-bridge formation.

Example 3

How many bones are there in (a) the human vertebral column and (b) the adult skull (including ear ossicles and hyoid)?

Answer: (a) Vertebral column = 26 bones (7 cervical, 12 thoracic, 5 lumbar, 1 sacrum, 1 coccyx). (b) Skull = 29 bones (8 cranial + 14 facial + 6 ear ossicles + 1 hyoid).

Example 4

Classify the following joints: (i) shoulder, (ii) knee, (iii) between atlas and axis, (iv) skull sutures.

Answer: (i) Ball and socket, (ii) Hinge, (iii) Pivot, (iv) Fibrous (fixed) joint.

Example 5

A patient shows muscle fatigue and weakness from an auto-immune attack at the neuromuscular junction. Name the disorder.

Answer: Myasthenia gravis.

Example 6

Give two differences between red and white muscle fibres.

Answer: Red fibres have more myoglobin and mitochondria and respire aerobically, contracting slowly without easy fatigue; white fibres have less myoglobin, respire anaerobically, and contract fast but fatigue quickly.


Important Questions for Board Exams

1-Mark Questions (VSA)

  1. Differentiate between movement and locomotion with one example each.
  2. Name the contractile proteins of the thin and thick filaments.
  3. What is the functional unit of a muscle called?
  4. Name the disorder caused by deposition of uric acid crystals in joints.
  5. Which ion is stored in the sarcoplasmic reticulum?

2–3-Mark Questions (SA)

  1. Describe the structure of a sarcomere, naming the A-band, I-band, H-zone, Z-line and M-line.
  2. Differentiate between red and white muscle fibres (any three points).
  3. Name and give one example each of any three types of synovial joints.
  4. Distinguish between the axial and the appendicular skeleton with examples.

5-Mark Questions (LA)

  1. Explain the sliding filament theory of muscle contraction in detail.
  2. Describe the structure of a skeletal muscle from the whole muscle down to the myofibril.
  3. Give an account of the human skeletal system, listing the bones of the axial and appendicular skeleton.

Quick Revision Points

  • All locomotion is movement, but not all movement is locomotion
  • Three movements: amoeboid (WBCs, pseudopodia), ciliary (trachea, oviduct), muscular (limbs)
  • Sarcomere = region between two Z-lines = functional unit of muscle
  • A-band = myosin (dark); I-band = actin (light); H-zone = only myosin; M-line at centre
  • Thin filament: actin + tropomyosin + troponin; Thick filament: myosin (meromyosin, head = cross-bridge)
  • Sliding filament theory: actin slides over myosin; I-band & H-zone shorten, A-band unchanged
  • Ca²⁺ binds troponin → exposes active sites → cross-bridge → power stroke (needs ATP)
  • Red fibres: more myoglobin, aerobic, slow, fatigue-resistant; White: less myoglobin, anaerobic, fast
  • Skeleton = 206 bones: axial (80) + appendicular (126)
  • Vertebral column = 26; skull = 29; ribs = 12 pairs (7 true, 3 false, 2 floating)
  • Joints: fibrous (fixed), cartilaginous (slight), synovial (free: ball-socket, hinge, pivot, gliding, saddle)
  • Disorders: myasthenia gravis (auto-immune NMJ), tetany (low Ca²⁺), gout (uric acid), osteoporosis (low oestrogen), arthritis

Next Chapter: Chapter 18 - Neural Control and Coordination

🃏 Flash Cards: Locomotion and Movement

Class 11 Zoology – swipe through all 9 cards to understand the whole chapter.

🏃Start here1/9

Movement vs Locomotion

Movement is any change in position of a body part; locomotion moves the whole body to a new place.

All locomotion is movement, but not all movement is locomotion

Heartbeat & peristalsis = movement, NOT locomotion.

  • Locomotion = walking, swimming, flying (body relocates)
  • Drives: food, shelter, mate, breeding grounds, escape predators
  • Movement is a defining feature of all living organisms
🦠Cell movements2/9

Three Types of Movement

Human cells show amoeboid, ciliary and muscular movement.

Amoeboid (pseudopodia · actin) · Ciliary (cilia) · Muscular (muscle fibres)

Muscular is the most prominent and underlies locomotion.

  • Amoeboid: macrophages & leucocytes (WBCs), uses actin microfilaments
  • Ciliary: mucus in trachea, ovum in fallopian tube
  • Muscular: contraction of muscle fibres moves limbs, jaws, tongue
💪Muscle types3/9

Muscle Tissue

All muscle is mesodermal; three types differ in striations and control.

Skeletal (striated · voluntary) · Smooth (non-striated · involuntary) · Cardiac (striated · involuntary)

Cardiac is striated yet involuntary — found only in the heart.

  • Skeletal: attached to bones, voluntary
  • Smooth (visceral): gut & vessel walls, involuntary
  • Cardiac: heart only, striated but involuntary
🧬Core structure4/9

Fibre to Sarcomere

A skeletal muscle nests fibre → myofibril → sarcomere, the functional unit between two Z-lines.

Sarcomere = ½ I-band + A-band + ½ I-band

A-band = dark (myosin); I-band = light (only actin), bisected by Z-line.

  • Fibre is a syncytium (multinucleate); membrane = sarcolemma
  • Sarcoplasmic reticulum stores Ca2
  • A-band centre has the H-zone, crossed by the M-line
🔗Key proteins5/9

Contractile & Regulatory Proteins

Thick filament is myosin; thin filament is actin with troponin and tropomyosin.

Contractile: actin, myosin · Regulatory: troponin, tropomyosin

Myosin head (HMM) carries ATPase + binding sites for ATP and actin.

  • Thin filament: 2 F-actin strands (polymers of G-actin)
  • Tropomyosin runs alongside, troponin sits at intervals
  • Myosin tail = LMM; head forms the cross-bridge
Core mechanism6/9

Sliding Filament Theory

Thin filaments slide over thick filaments, shortening the sarcomere — filaments themselves do NOT shorten.

ACh → action potential → Ca2⁺ release → troponin → cross-bridge → power stroke (ATP)

I-band & H-zone shorten; A-band length stays constant.

  • Ca2⁺ binds troponin → tropomyosin uncovers actin active sites
  • ATP needed twice: power stroke AND to detach the myosin head
  • Fatigue: lactic acid from anaerobic glycolysis; red=aerobic, white=anaerobic
🦴Skeleton counts7/9

Axial & Appendicular Skeleton

The adult human skeleton has 206 bones, split into axial and appendicular.

206 = Axial (80) + Appendicular (126)

Vertebral formula C7 T12 L5; femur longest, stapes smallest.

  • Axial 80: skull region 29 + vertebral column 26 + sternum 1 + ribs 24
  • Ribs: 1-7 true, 8-10 false, 11-12 floating
  • Appendicular 126: limbs (4×30=120) + girdles 6 (pectoral + pelvic)
🔧Joints8/9

Fibrous, Cartilaginous, Synovial

Joints are classified by how much movement they allow.

Fibrous (immovable) · Cartilaginous (slightly movable) · Synovial (freely movable)

Synovial cavity & fluid are unique to synovial joints.

  • Fibrous: skull sutures; Cartilaginous: between vertebrae
  • Synovial subtypes: ball-and-socket (shoulder/hip), hinge (knee/elbow)
  • Pivot (atlas-axis), gliding (carpals), saddle (thumb carpal-metacarpal)
🩺Disorders9/9

Muscular & Skeletal Disorders

Each disorder pairs to a specific site and cause — that is what NEET tests.

Low Ca2⁺ → tetany · Low oestrogen → osteoporosis · Uric acid → gout · Autoimmune NMJ → myasthenia gravis

Tetany is LOW calcium (never reverse it).

  • Myasthenia gravis: autoimmune attack on neuromuscular junction
  • Osteoporosis: ↓ bone mass, post-menopausal low oestrogen
  • Gout: uric-acid crystals inflame joints; arthritis = joint inflammation
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📝 Practice Locomotion and Movement — 10 NEET PYQs
Real previous-year questions · with answers & solutions
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Q1NEET 2021
During muscular contraction, which of the following events occur? (I) ‘H’ zone disappears (II) ‘A’ band widens (III) ‘I’ band reduces in width (IV) Myosin hydrolyses ATP, releasing the ADP and Pi (V) Z-lines attached to actins are pulled inwards.
Correct answer: A. On contraction, thin filaments slide inward: the H-zone shrinks/disappears (I, true), the I-band narrows (III, true), myosin’s ATPase hydrolyses ATP for the power stroke (IV, true), and the Z-lines are pulled toward the centre (V, true). Statement II is false — the A-band width equals the thick-filament length, which never changes. So the correct events are I, III, IV and V.
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Q2NEET 2021
Match List I (bone/structure) with List II (feature): A. Scapula B. Cranium C. Sternum D. Vertebral column with 1. Cartilaginous joints 2. Flat bone 3. Fibrous joints 4. Triangular flat bone.
Correct answer: C. Scapula is a triangular flat bone (4); cranial bones meet at immovable fibrous joints/sutures (3); sternum is a flat bone (2); adjacent vertebrae are joined by cartilaginous joints (1). So A-4, B-3, C-2, D-1.
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Q3NEET 2021
A chronic autoimmune disorder affecting the neuromuscular junction, leading to fatigue, weakening and paralysis of skeletal muscle, is called:
Correct answer: C. Myasthenia gravis is an autoimmune disorder in which antibodies block acetylcholine receptors at the neuromuscular junction, causing fatigue and progressive muscle weakness/paralysis. Arthritis and gout affect joints; muscular dystrophy is a genetic muscle degeneration.
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Q4NEET 2020
Match Column I with Column II: A. Floating ribs B. Acromion C. Scapula D. Glenoid cavity with 1. Located between second and seventh ribs 2. Head of humerus 3. Clavicle 4. Do not connect with the sternum.
Correct answer: C. Floating ribs (11th–12th) do not connect to the sternum (4); the acromion process of the scapula articulates with the clavicle (3); the scapula lies between the 2nd and 7th ribs on the dorsal thorax (1); the glenoid cavity receives the head of the humerus (2). So A-4, B-3, C-1, D-2.
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Q5NEET 2019
Match the joints with the bones involved: 1. Gliding joint 2. Hinge joint 3. Pivot joint 4. Saddle joint with (i) Between carpal and metacarpal of thumb (ii) Between atlas and axis (iii) Between carpals (iv) Between humerus and ulna.
Correct answer: A. Gliding joint is between the carpals (iii); hinge joint is between the humerus and ulna at the elbow (iv); pivot joint is between the atlas and axis (ii); saddle joint is between the carpal and metacarpal of the thumb (i). So 1-iii, 2-iv, 3-ii, 4-i.
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Q6NEET 2019
Which of the following muscular disorders is inherited (genetic)?
Correct answer: A. Muscular dystrophy is an inherited disorder (e.g. due to absence of the dystrophin protein) causing progressive muscle degeneration. Myasthenia gravis is autoimmune, botulism is bacterial food poisoning (Clostridium botulinum), and tetany results from low blood calcium — none are inherited.
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Q7NEET 2018
Calcium is important in skeletal muscle contraction because it:
Correct answer: C. Released Ca²⁺ binds the troponin (TnC) subunit, shifting tropomyosin off the actin active sites so myosin heads can bind and form cross-bridges. It does not detach myosin (that needs fresh ATP), does not bind myosin’s ATPase, and does not block cross-bridges — it enables them.
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Q8NEET 2017
The pivot joint between the atlas and axis is a type of:
Correct answer: C. A pivot joint is a sub-type of freely movable synovial joint (it has a synovial cavity). The atlas–axis pivot allows the head to rotate. It is not a fibrous or cartilaginous (limited/no-movement) joint; ‘saddle’ is a different synovial sub-type.
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Q9NEET 2016
Smooth muscles are:
Correct answer: A. Smooth (visceral) muscle is involuntary, spindle-shaped (fusiform), uninucleate and non-striated, found in the walls of hollow visceral organs. ‘Striated’ and ‘voluntary’ describe skeletal muscle, so the other options are wrong.
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Q10NEET 2013
The H-zone in the skeletal muscle fibre is due to:
Correct answer: C. The H-zone is the lighter central part of the A-band where the thin (actin) filaments do not reach — i.e. the gap between the two sets of actin filaments, a region of myosin only. It is not an absence of myofibrils, and myosin spans the whole A-band, so the other options are wrong.
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Frequently Asked Questions

What is the difference between movement and locomotion?

Movement is any change in position of a body part, while locomotion is movement that relocates the whole organism to a new place such as walking, swimming or flying. All locomotion is movement, but not all movement is locomotion, for example heartbeat and peristalsis are movements but not locomotion.

What is the sliding filament theory of muscle contraction?

It states that during contraction the thin actin filaments slide over the thick myosin filaments, shortening the sarcomere, while the filaments themselves do not shorten. A motor signal releases acetylcholine and then calcium, calcium binds troponin to expose actin sites, and myosin cross-bridges pull using ATP, which shortens the I-band and H-zone while the A-band stays the same length.

How many bones are in the human skeleton and how are they divided?

The adult human skeleton has 206 bones, divided into the axial skeleton with 80 bones and the appendicular skeleton with 126 bones. The axial skeleton includes the skull, vertebral column, sternum and ribs, while the appendicular skeleton includes the limb bones and the pectoral and pelvic girdles.

Is Locomotion and Movement important for NEET?

Yes, it is part of the NCERT Class 11 Biology syllabus and is a high-yield human physiology chapter for NEET, usually contributing one to two questions. Favourite areas are sarcomere structure, the sliding filament steps, bone counts, joint types and the muscular and skeletal disorders.

What is the difference between tetany and osteoporosis?

Tetany is rapid muscle spasms caused by a low level of calcium ions in the body fluid, whereas osteoporosis is an age-related decrease in bone mass and strength most often linked to low oestrogen levels after menopause. In short, tetany is a calcium-deficiency muscle disorder and osteoporosis is a bone-density disorder.

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