Lecture 15 Flashcards

1
Q

How is thermoregulation behaviourally controlled?

A

Repositioning the body in the environment to control body temperature.

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2
Q

How is thermoregulation physiologically controlled?

A

Immediate neural responses E.g. sweating, panting.

Long term adaptation/acclimatisation E.g. changes in insulation/capacity to alter metabollic heat.

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3
Q

Define tolerance.

A

Capacity to endure continued environmental conditions without an adverse reaction. Factors like temperature, salinity etc.

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4
Q

How does tolerance differ?

A

Differs between species, within and between populations, change between season, life stages condition, age etc.

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5
Q

What is the zone of tolerance?

A

Central range where an animal is most comfortable. Bounded by upper and lower zone of physiological stress within which organisms can survive for an indefinite period of time.

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6
Q

What effects heat tolerance?

A

Thermal history E.g. exposure to warm temperatures increases heat tolerance but decreases cold tolerance.
Seasonal changes in temperature.

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7
Q

What are heat shock proteins?

A

Proteins present in all cells that limit the consequence of adverse conditions (stress). Limit consequences of damage from stress and facilitate cellular recovery.

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8
Q

What are the primary functions of HSPs?

A

Promote proper folding/refolding of proteins.
Prevent potentially damaging interactions between proteins.
Aid in disassembly of protein aggregates.

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9
Q

How do HSPs act as molecular chaperones?

A

They stabilise other proteins and minimise probability of inappropriate reactions. Involved in folding, assembly, regulation and degradation of other proteins.

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10
Q

How are HSPs highly conserved?

A

They are present in all major components of all cells of all animals, plants and prokaryotes.

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11
Q

What are some examples of stress that cause HSP expression?

A

High/low temperatures, pH shift (affects ionic bonds), toxic substances/pollution, physical stress, hypoxia.

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12
Q

In what ways can HSPs be expressed?

A

Constituatively (all of the time),
increased during/after stress,
Exclusively induced by stress.

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13
Q

Describe the HSP response.

A
  1. Stress causes proteins to denature.
  2. Denatured proteins are detected.
  3. HSP proteins are produced which don’t denature as they have better hydrogen bonds and secondary structure.
  4. HSPs act as molecular chaperones and help proteins fold back to their original conformation.
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14
Q

What are the secondary functions of HSPs?

A

Aid immune response as they are normally found inside cells so if detected outside this signals cell damage. They help present antigens from diseased cells to T-cells.

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15
Q

What are the costs of HSPs?

A

They are energetically costly to produce

E.g. Drosophila engineered to have more HSP genes developed slower and had higher mortality.

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16
Q

What are the effects of sub-zero temperatures?

A

Fast cooling: ice crystals form that damage cells.
Slow cooling: External fluid freezes which increases the solute concentration and causes water to leave the cells by osmosis and cells to shrink.

17
Q

What are the 2 strategies for dealing with sub-zero temperatures?

A

Freeze avoidance and freeze tolerance.

18
Q

What is freeze avoidance?

A

Avoiding freezing by keeping the bodily fluids liquid. Mostly in the Northern hemisphere where cold is expected seasonally and for long periods of time.

19
Q

What are the 3 strategies of freeze avoidance?

A
  1. Selecting a dry hibernation site where no ice nucleation from an external source can occur.
  2. Physical barrier such as a wax-coated cuticle that provides protection against external ice across the cuticle.
  3. Depressing the temperature at which body fluids freeze by Supercooling or cryoprotectant synthesis.
20
Q

What is supercooling?

A

Removing/deactivating ice nucleating agents from the gut/intracellular so the freezing point of water falls to -42 degrees. A physical process.

21
Q

What is cryprotectant synthesis?

A

Increasing solute concentration, usually glycerol which attracts water to retain water inside cells and reduce dehydration. An alteration of biochemistry.

22
Q

What is freeze tolerance?

A

Tolerating the formation of internal ice and the effects of ice formation and dehydration. Mostly in the S. hemisphere where seasonal cold isn’t as extreme or long lasting. Also in the Arctic where freezing occurs for long periods up to 9 months.

23
Q

What are the 3 strategies of freeze tolerance?

A
  1. Limit supercooling by freezing body fluids at relatively high temperatures to control ice formation.
  2. Produce ice structuring (antifreeze) proteins which bind to small ice crystals and inhibit growth.
  3. Produce ice nucleating proteins to control ice formation at relatively high temperatures to avoid a sudden total freeze.
24
Q

What are the advantages of producing ice nucleating proteins to an insect?

A

Allows moderation of ice growth rate so insect can adjust to mechanical and osmotic pressures of ice formation.

25
Q

How does the arctic wooly bear moth withstand the cold?

A

Freeze tolerance: withstands -70 during diapause by accumulating cryprotectants like glycerol and forming a hiberculum to inhibit nucleators.

26
Q

How does the Goldenrod gall moth larvae withstand the cold?

A

Freeze avoidance by supercooling from -14 to -38. Decreases water content and increases glycerol content.

27
Q

How does the wood frog withstand the cold?

A

Strategy combo of supercooling and tolerating 48% of total body fluids freezing. No anticipatory accumulation of cryoprotectants.

28
Q

How does the red bark beetle larvae survive?

A

High concentration of glycerol and ice structuring proteins. Forms a glassy substrate that doesn’t freeze.

29
Q

How does the snow flea survive?

A

Synthesises ice structuring proteins which can be made synthetically to store human organs for transplant.