Locomotor Flashcards

1
Q

Use anatomical terms to correctly describe the position or orientation of parts of the body.

A

○ Abaxial – away from longitudinal axis
○ Axial – towards longitudinal axis

○ Palmer – rear surface of forepaw
○ Plantar – rear surface of hind paw

○ Medial – towards median plane
○ Lateral – away from median plane

○ Rostral – towards nose
○ Cranial – towards head
○ Caudal – towards tail

○ Distal – away from body
○ Proximal – closer to body

○ Dorsal – towards the spine/top (up)
○ Ventral – towards the tummy/ground (down)

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2
Q

Use appropriate terminology to describe the view of an Anatomical Terminology photograph or medical image (e.g. X ray, CT scan).

A

○ Median/Mid-sagittal – symmetrical left & right

○ Sagittal/parasagittal/paramedian – unsymmetrical left & right

○ Transverse – divides cranial/caudal OR distal/proximal (cross section)

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3
Q

Describe how bipedal and quadrupedal animals are adapted for posture and movement.

A

○ Quadrupeds
§ Stability (large base of support)
§ Differentiate function (forelimbs manoeuvrability, hindlimbs power)

○ Bipedal
§ Free thoracic forelimbs (flight, prehension, brachiation)
○ Large feet (wide base of support)

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4
Q

Explain major similarities and differences in body form between bipeds and quadrupeds.

A

○ Quadrupeds
§ Elbows & knees oppositely orientated (homologous joints)
§ Larger proximal mass & springier in hindlimb
§ Forelimb uprightness

○ Bipedal
§ Walking – long HL & short FL, plantigrade, upright spine (centre of mass)
§ Jumping – crouched limbs, proximal muscle mass, thin distal limbs
§ Flight – HL perch body weight & catch prey, FL wings

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5
Q

Discuss anatomical adaptations of animals for specific functions.

A

○ Cheetah (Carnivore) – powerful psoas muscles, HL bone long (longer strides)

○ Horse (Ungulate) – long limbs (long distance), distal limb low mass (stride rate), limb elongation (stride length)

○ Capybara (Rodent) – HL soleus muscle for water propulsion, semi aquatic

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6
Q

What the major patterns and processes in evolution are

A

○ Patterns
§ Anagenesis – gradual linear transformation of 1 species into another
§ Cladogenesis – rapid branching of species (2+ spit at each node)

○ Processes
§ Sources of variation (prodigy produced)
□ Mutation, recombination, phenotypic plasticity & constraints
§ Modifiers of variation (next gen prodigy)
○ Natura selection, sexual selection, genetic drift

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7
Q

How a phylogeny is used

A

○ Diversification of lineages through evolution

○ Computer algorithms find pattern (phylogeny) that represents best estimate of evolutionary patterns

○ Shared novel traits (not primitive traits)

○ Track pattern of trait evolution at any scale

○ Test convergent evolution

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8
Q

What adaptation is, and what about evolution is non-adaptive

A

○ A trait that enhances fitness and that arose historically as a result of natural selection for its current biological role.

○ Key innovators lead to adaptive radiation (explosion of speciation at a lineage) = phenotypical & ecological diversification

○ Non-adaptive forces are primarily random & not influenced by environment (mutation, genetic drift, and recombination)

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9
Q

Why evolution is relevant to vet students

A

○ host parasite, drug disease arms races

○ phylogeny similarity - similar treatments work better on closely related species

○ Harnessed by humans for breeding artificial selection (health problems arise when animal experience environments they did not evolve in)

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10
Q

Classify bone according to shape (e.g. long bones, flat bones), and giving examples explain how shape relates to function.

A

Long - Cylinder (longer than wide), Leverage, e.g. Femur, tibia, fibula

Short - Cube (approx. equal lengths), Stability, support & some motion, e.g. Carpels & tarsals

Flat - Thin and curved, Points for muscle attachment & protect internal organs e.g. Ribs, cranial bones

Irregular - Complex shapes, Protect internal organs, Vertebrae & facial bones

Sesamoid - Small & round (embedded in tendons), Protect tendons from compressive forces, e.g. Patellae

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11
Q

Describe the macroscopic architecture of bone and explain how this organisation relates to function

A

○ Periosteum – thin layer of connective tissue lining outside of bone

○ Cartilage – flexible material at bone edges to absorb impact

○ Epiphysis – next to cartilage at bone end, houses red bone marrow (RBC produced)

○ Epiphysis plate – next to epiphysis, extra bone produced to elongate pre-puberty

○ Metaphysis – contain epiphysis plate, expands neck region

○ Diaphysis – in main bone shaft, house bone marrow, site of ossification

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12
Q

Recount the anatomical relationship between bone and peri- and endosteum. Describe the functions of these tissues.

A

○ bone is an organ and therefore subject to continual adaptation processes.

○ Bone Function
§ Cortical (compact) bone – thick, dense & stiff
§ Trabecular (spongy) bone – cobweb, less dense , handle loads in loco

○ Periosteum/Endosteum Function
§ Peri – blood supply, bone rescaling & maintenance, lines outside
○ Endo – lines inside cavity in long bones outside the medullary cavity

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13
Q

(part 1) Describe gross skeletal muscle and tendon structure and how muscle and tendon are arranged in the locomotor system

A

○ Gross Skeletal Muscle Structure
§ Origin – where muscle directly attaches to bone (top)
§ Muscle belly – thick fleshy central part & tapers at each end (proximal)
§ Connective tissues – between muscle fibres
§ Tendon – attaches muscle to bone in insertion site (distal)
§ Aponeurosis – bridge between muscle/tendon
○ Insertion – site on bone where tendon attaches

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14
Q

(part 2) Describe gross skeletal muscle and tendon structure and how muscle and tendon are arranged in the locomotor system

A

○ Skeletal Muscle Arrangement (striated)
§ Aponeurosis – bridge between muscle/bone OR muscle/tendon
§ Epimysium – thin connective tissue that binds muscle belly together
§ Muscle belly – thick fleshy central part & tapers at each end
§ Perimysium – connective tissue binding each fascicle
§ Fascicle – bundle of muscle fibre subunits
§ Endomysium – surround muscle fibres
§ Sarcolemma – cell membrane around muscle fibres
§ Muscle fibre – primary muscle cell unit
□ Sarcomas – series of myofilaments between z lines
□ Myofibril – multiple peripheral nuclei
○ Contractor proteins – actin & myosin

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15
Q

(part 3) Describe gross skeletal muscle and tendon structure and how muscle and tendon are arranged in the locomotor system

A

Tendon Structure
○ Proximal – short & fat
○ Distal – long & thin

○ Triple helix - 3 polypeptide chains
○ Collagen fibril – multiple triple helices
○ Collagen fibre – multiple fibrils
○ Subfascicles – multiple fibres

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16
Q

Discuss the roles/functions of muscle in the body and particularly in locomotion & compare and contrast the structure of skeletal, smooth and cardiac muscle

A

○ Muscle roles
§ Tendon – minimise distal limb mass, elastic energy storage, direct join
muscle power to bone
§ Skeletal – joint movement & stabilisation, posture control, shivering
§ Smooth – mastication, swallowing, digestion, birthing, dilation/constriction
§ Cardiac – maintain cardiac rhythm

○ Muscle Structure
§ Tendon – triple helix strands creating collaged fibres
§ Skeletal – myofibril fibres containing contractor proteins actin & myosin
(striated)
§ Smooth – un-striated, involuntary, long spindle-shaped cells, surrounding
connective tissue bind cells into sheets/layers
○ Cardiac – striated & cylindrical, involuntary, cells branch & create fibrous network

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17
Q

Explain how tendon contributes to locomotion

A

○ Tendon springs – store & release elastic energy = economical distal limb

○ Power amplifiers – stretched tendon recoils faster than muscle = higher power output

○ Minimise distal limb mass (horses) – swing efficiently

○ Joins muscle direct to bone – muscle forces transmit to skeleton efficiently

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18
Q

Describe muscle architectural design and explain how this influences muscle function

A

○ Pennate muscles
§ feather-like fibre arrangement
§ short fibres orientated towards muscle axis
§ able to pack in more sarcomere contractile units = increase muscle PCSA &
force (economical)
§ e.g. serratus ventralis – attaches scapula to trunk

○ Parallel muscles
§ Fibres run directly parallel to muscle axis
§ More sarcomeres in series = higher muscle fibre shortening
§ Moves joints in a greater range of motion
§ E.g. pectoral muscle – retract limb

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19
Q

Describe the basic structure of a synovial joint and the tissues of which a synovial joint is composed & explain how joint tissue and structure facilitate effective joint function

A

○ Ligament – stabilise joint (outside & inside joint)

○ Joint cavity – synovial fluid filled space that surrounds whole joint & separates the two bones

○ Fibrous tissue layer – protects joint cavity

○ Synovial membrane – lines joint cavity & secretes synovial fluid

○ Synovial fluid – lubricates joint & provides nutrition for hyaline articular cartilage ends of the bones

○ Articular hyaline cartilage – bone interface at synovial joint, low friction, no nerves/blood vessels

○ Menisci – increase range of movement & shock absorbers (2 in stifle joint)

○ Bursae – synovial fluid sacs (found in other joint types), reduce friction

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20
Q

Classify synovial joints according to their action. Give examples of types of synovial joints in the body.

A

Planar - Gliding, Slide bony surface over another, Between rows of carpal/tarsal bones

Hinge - Uniaxial, Movement in 1 plane, Humeroulnar

Pivot - Uniaxial, Peg in ring (rotation), Atlantoaxial joint

Condylar - Biaxial, Convex surface sitting on concave surface, Tarsus/hock & femorotibial (stifle)

Saddle - Biaxial, Convex & concave surfaces @ right angle, Distal interphalangeal (dog claw flex & extend)

Ball & Socket - Triaxial, Big movement range, Hip and shoulder

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21
Q

List the molecular components of the Extracellular Matrix (ECM) and discuss their structural and mechanical properties.

A

○ Network of secreted macromolecules – maintains integrity, protection, cell communication

○ Elastin – allows deformation, coiled when relaxed, cross linked when stretched

○ Collagen – triple helix = high tensile strength (microfibrils –> fibrils –> fibres)

○ Glycosaminoglycans (GAGs) – anti-compressive hydrophilic, lubricant e.g. synovial fluid

○ Proteoglycans = Gag + protein, anti-compressive e.g. keratin sulfate & chondroitin sulfate

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22
Q

Describe and compare the macro and microscopic structure of different musculoskeletal tissues (bone, tendon, ligament, cartilage, muscle).

A

○ Bone, tendon, muscle, ligament see previous answers

○ Cartilage structure
§ Superficial tangential zone = 85% collagen to resist tension by shearing
§ Middle transitional zone = mostly proteoglycans, oblique arranged collagen,
transition from shearing to compressive forces
○ Deep radial zone = collagen fibres vertical to resist compression forces

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23
Q

Explain how the gross structure and molecular and cellular composition of musculoskeletal tissues relate to their function and mechanical properties.

A

○ Cell types (blasts, clasts & cytes) & functions
§ Tendon (TENO) = store & release elastic energy, economical locomotion
§ Ligaments (FIBRO) = stabilise joints
§ Cartilage (CHONDRO) = mechanical joint loading, resist tension produced
by shearing
§ Bone (OSTEO) = cytes support/maintain structure, blasts synthesise matrix,
clasts absorb bone

○ Cellular composition
§ Tendon – collagen type 1 (86%), proteoglycan (15%), elastin (2%), water
§ Ligament – collagen type 1 (75%), proteoglycan (15+%)
§ Cartilage – collagen type 2 (90%), proteoglycan (10-20%), water (68%)
○ Bone – collagen type 1 (90% of 30% organic component), hydroxyapetite
(organic)

24
Q

Describe the influence of mechanical loading on ECM turnover and tissue adaptation processes.

A

○ ECM constant turn over due to mechanical loading
§ - cytes = transmits forces to cells
§ – blasts = experience force & build more tissue or will signal
§ – clasts = receive signal & produce response

○ Tissue adaptation
§ Mesenchymal cells – undifferentiated stem cells
§ Cells differentiate under mechanical loads
§ Tendons & ligaments – pulled unidirectional
○ Cartilage – compressed one side & pulled the other (omnidirectional)

25
Specify the cellular and molecular composition of bone tissue
○ Osteocytes = support/maintain structure ○ Osteoblasts = synthesise matrix ○ Osteoclasts = absorb bone
26
Describe the process of bone formation in the developing animal
○ Intramembranous ossification § Flat bone – osteoblasts lay down between 2 layers of fibrous connective tissue with no cartilage template ○ Endochondral ossification § Bone collar formation around hyaline cartilage model § Primary ossification centre in diaphysis bone region □ Mesenchymal tissue excrete pre-mineralised ECM (osteoid) = bone precursor tissue § Cartilage replaced with bone via osteoblasts & extends to bone edges § Secondary centre of ossification at epiphysis region § Osteoclasts remove bone rom centre of diaphysis to form medullary cavity ○ Artery invasion & blood vessel formation (vascularise tissue)
27
Describe the process of bone growth in the young animal
○ Epiphysial growth plate allows bone to lengthen while animal grows ○ LHS EGP high number of chondrocytes ○ Cells increase in number & size (hypertrophy) & elongates from LHS across diaphysis region ○ Final size – EGP becomes a line & changes function
28
Discuss nutritional and hormonal factors that can affect bone growth
○ Nutritional factors § Dietary calcium & phosphate salts § E.g. Vitamin A, B12, C, D, K § Absorption depends on calcitriol (hormone in vitamin D presence) ○ Hormonal factors § Calcitonin & parathyroid hormone calcium = regulate metabolism § Insulin, growth hormone & thyroxine = bone growth ○ Oestrogen = growth plate closure & osteoblast activity (ossify cartilage)
29
Describe the process of bone remodelling and explain why it occurs
○ Cyclical process § Osteoclasts form & attach to bone matrix § Reabsorption - osteoclasts secrete breaking bone down enzyme & apoptose themselves § Reversal – area is populated by osteoblasts § Formation – osteoblasts synthesise organic matrix & regulate its mineralisation, entomb selves into matrix = become osteocytes § Forms lamellar bone (strong & slow production) or woven bone (weak & rapid production) ○ Why it occurs § Maintains mechanical strength from microfractures ○ Mineral homeostasis – stores calcium & phosphorus
30
Discuss the trade-offs between locomotor performance and risk of injury.
○ Performance – HL muscle mass, thick long tendons, fast twitch, anaerobic resp, remodelling (support load change) ○ Risk of injury – traumatic single event or repetitive cyclic stress, micro-ruptures to bone fractures
31
Discuss the relationships among loading, use/disuse, tissue damage and repair, and how disruption of the balance among these leads to injury.
○ Loading – overloading stress from a traumatic event overcomes safety factor of structure ○ Repetitive use – cyclic stress induced damage overcomes adjustment/repair capacity ○ Tissue damage & repair – woven bone (quick & weak)
32
Explain the concept of safety factors, and why some structures have lower safety factors than others.
○ Safety factor - limb bones have a capacity to withstand greater loads than they usually experience ○ Lower/higher factors depend on the kind of mechanical load placed upon them
33
Describe the cellular and molecular mechanisms involved in muscle contraction.
○ Calcium ions diffuse from sarcoplasmic reticulum into myofibrils ○ Calcium binds to troponin molecule & changes shape ○ Myosin-binding site on actin now free for ADP + P head ○ Actin & myosin filaments slide over each other ○ cross-bridges form between heads of actin & myosin filaments ○ cross-bridges swing through an arc (pull thin filament past thick ones) = sarcomere shortens ○ binding of ATP onto myosin head = cross-bridges detach from thin filament release of energy allows myosin head to reattach further away (move back)
34
Describe why skeletal muscle contraction requires energy, and discuss possible sources of this energy.
○ energy needed to produce contractions ○ energy sources § 1. Phosphorylation of ADP by creaine phosphate (short duration only) § 2. Phosphorylation of ADP in cytosol (anaerobic) (2ATP for every glucose) ○ 3. Oxidative phosphorylation of ADP in mitochondria (aerobic) (34 ATP)
35
Compare the properties of the main types of skeletal muscle fibre.
○ Slow oxidative muscle cells (type 1) § Weaker than faster muscle cells but are fatigue resistant § Use aerobic respiration (high oxidative capacity) § Contract & twitch slower, but sustain forces for a longer duration ○ Fast glycolytic (Type IIb) § Twitch very quickly (high ATPase activity) § ATP responsible for causing the muscle myosin head to reset (quicker reset = twitch/move quicker) § Good at producing glycolysis (high glycolytic pathway) § Large, strong, high force, run out of energy quickly ○ Fast oxidative glycolytic § Uses oxidative & glycolytic pathways § quicker than type 1 but slower than type2b § Decent capacity for oxidative phosphorylation & glycolytic pathway (aerobic & anaerobic)
36
Name and describe the types of muscle contraction and give examples of when each might be used in a standing or moving animal.
○ Isometric – muscle contract (not shorten) e.g. horse standing stationary ○ Concentric – force exceeds load e.g. pick up leg ○ Eccentric – load exceeds force e.g. place leg back down
37
Recall the basic layout of the nervous system
○ 1. Central (CNS) § Brain & spinal cord ○ 2. Peripheral (PNS) § Efferent (Motor) - outgoing signals, trigger muscles to contract □ Somatic (Skeletal muscle) - aware of □ Autonomic (Cardiac/ smooth muscle, exocrine glands) § Afferent (Sensory) □ Somatic (awareness of) ○ Visceral (unaware of)
38
Describe the structure of a neuromuscular junction
1. Axon - of motor neuron w/ myelin sheath 2. Axon terminal – where axon ends & bulb begins 3. Pre-Synaptic bulb – contains terminal buttons, voltage-gated calcium channels and vesicles of neurotransmitters 4. Synaptic cleft – gap where neurotransmitter is released into 5. Motor end plate – neurotransmitter gated channels, voltage gated potassium channels, acetylcholinesterase
39
(part 1) Discuss the basic mechanism of synaptic communication and the events at a NMJ that lead to an action potential in a skeletal muscle fibre
○ Pre-synaptic axon o An action protentional (voltage) will come down motor neuron axon o The action potential jumps down axon due to insulated myelin sheaths o Reaches axon terminal · Voltage-gated calcium channels · Action potential triggers calcium channel proteins to reconfigure & allow calcium to enter from extracellular matrix into the axon · Calcium in axon will bond to proteins as it moves to the internal surface of the axon terminal membrane (towards synapse) · Calcium & proteins grab vesicles & fuse the vesicles to the membrane & release their contents into the synaptic gap in high density ○ Synaptic gap · Passive stage - waiting for red acetylcholine molecules within the vesicles to float down & interact with sarcolemma § Importance of large surface area & a short gap - diffusion distance across does slow it down ○ Fast animal movements = short gap, many acetylcholine molecules released, large surface area & many receptors to receive the acetylcholine
40
(part 2) Discuss the basic mechanism of synaptic communication and the events at a NMJ that lead to an action potential in a skeletal muscle fibre
○ Post-synaptic · Acetylcholine bonds to ligand-gated channels (respond to interaction with other molecules) · Ligand-gated channels allows § large amounts of sodium into the muscle cells § Small amounts of potassium out of muscle cells · After sodium enters the cells, a new voltage potential is produced across cell membrane § which stimulates voltage-gated sodium channels · This allows more sodium in & action potential will travel rapidly & propagate across cell until it completes § Causes muscle cells to be depolarised ○ Acetylcholinesterase protein § Mechanism to stop passively diffusing acetylcholine from bonding to ligand-gated sodium-potassium channels § Enters extracellular matrix, bonds to sporadic acetylcholine & breaks them down to stop stimulating ligand-gated channels
41
Explain the mechanism of excitation contraction coupling
○ Muscle action potential propagates an voltage differential into T tubule along cell membrane ○ Depolarisation of T-tubule causes opening of calcium channels between myosin & S.R. ○ Calcium released from Sarcoplasmic Reticulum ○ Calcium binds to troponin C ○ Affects tropomyosin & allow myosin start bonding to the actin & begin walking along actin strand pulling tropomyosin filaments together causing muscle contraction
42
Appreciate the concept of a skeletal muscle motor unit
○ how the nervous system controls the force generating capacity of muscles ○ Array of muscle fibres innervated by multiple different motor units ○ ratio of number of muscle fibres being triggered by each motor units determine how fine of an actuation is
43
Describe the role of the forelimb in locomotion
○ Roles – manoeuvrability, weightbearing, support & stability ○ Thoracic limb has evolved into a supporting structure of locomotor system ○ Thoracic girdle is reduced in cursors ○ Scapula slides on rib cage ○ Humerus large and robust ○ Radio ulnar articulation reduced/absent
44
Discuss differences in forelimb anatomical structure between the major veterinary species and how this relates to their locomotor behaviour
○ Distal forelimb Horse – minimise mass, store & release elastic energy, less requirement to control loss of digits ○ Tendon & ligaments Horse – long, elastic flexor tendons (deep digital & superficial digital) Dog – coupled with large proximal muscles (muscle control over digits) ○ Interosseus muscle Horse – none (only one digit) Dog – possess a lot to allow for individual movement of each digit ○ Foot & digits Horse – hoof (keratin) = ungulate Dog – digitigrade (bears weight on digits), metacarpal pads
45
Describe the role of the pelvic limb in locomotion
○ Pelvic limb = fixed to trunk via sacroiliac joint ○ Proximal pelvic limb robust = Enable to withstand loads imposed on them ○ Thoracic limb = Support weight and turning and breaking
46
Discuss differences in pelvic limb anatomical structure between the major veterinary species and how this relates to their locomotor behaviour.
○ Equine hindlimb · Huge propulsive muscles (gluteals and hamstrings) · Patella locking · Reciprocal apparatus · Reduced number of bones · Increased tendons distally · angular proximal limb, short robust femur, long & upright distal limb ``` ○ Canine hindlimb · joint stops to take more angulation · weight based solely on digits · calcaneus for weight support · More RoM at ankle and foot = more muscles ``` ○ Plantigrade hindlimb · hind foot fully contact with ground . long non-angular upper limb bones
47
Describe the kinetics and kinematics of fore and hind limbs during the stride cycle
○ Forces (kinetics) – GFR (support animal weight), muscle forces (limb movement), joint contract forces ○ Stance phase – high GRF, stabilise joint, resist over-extension of distal joint ○ Swing phase – no GRF, protract limb, clear foot off ground, prepare for stance
48
Know which muscle groups contribute to the various stages of the stride cycle
○ Hamstring group (hindlimb) – extend hip & flex stifle (main forward thrust) ○ Pectoral group (forelimb) – protracts, retracts & abducts forelimb
49
Compare the basic differences between gaits based on i) footfall patterns and ii) biomechanical principles
○ Walking · FF – RH,RF,LH,LF · Biomechanics – out of phase kinetic & potential energy ○ Trotting · FF – alternately balanced on diagonally opposite feet (LF/RH then RF/LH) · Biomechanics – in phase kinetic & potential energy (due to elasticity) ○ Canter/Gallop · FF – floating phase underneath body . Biomechanics – minimise collision forces
50
Explain why animals might chose to use particular gaits
○ Minimise GFR - reduce fatigue & musculoskeletal tissue impact ○ Energy efficient – change when oxygen consumption becomes costly
51
Appreciate how gait may differ from the norm due to injury/pathology
○ Forelimb lameness – nods head when non-lame leg impacts the ground ○ Hindlimb lameness – asymmetry vertical movement
52
Explain how the musculoskeletal system is arranged in animals adapted for terrestrial locomotion.
○ Bones, joints, cartilage, tendons, ligaments & muscles (See previous answers)
53
Explain the role of tendon in locomotion and how it interacts with muscle to enhance efficiency and power output.
○ minimise distal limb mass ○ elastic energy storage ○ attached to muscle and bone – enhances muscle power to bone
54
Discuss difference in limb morphology between different classes of mammal.
○ Plantigrade - surface of the whole foot touches the ground during locomotion ○ Digitigrade – only phalanges touch the ground ○ Unguligrade – singular toe touches ground
55
Relate cost of locomotion to mode of transport, body mass and morphology.
○ Swimming – lowest cost (energetically cheap) ○ Flying – energetically expensive but fast ○ Running – most expensive, moving centre of mass not smooth, support body weight (slows down) ○ Body mass – smaller the animal, more costly the locomotion