paper 2 required practicals Flashcards

(31 cards)

1
Q

What is a quadrat used for?

A

-To study the distribution of small organisms or estimate population sizes in a specific area.

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2
Q

What is meant by ‘abundance’ in ecology?

A

-The number of individuals of one species in a given area.

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3
Q

What do you record in each quadrat?

A

-The number of organisms of the species you are studying (e.g. daisies), or percentage cover.

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4
Q

What is the formula to calculate population size?

A

-Mean number of organisms per quadrat × total area ÷ area of one quadrat

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5
Q

Why is it important to take multiple quadrat samples?

A

-To calculate a reliable mean and account for random variation.

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6
Q

What are the control variables in the quadrat practical?

A

-Quadrat size, sampling method, and the environmental conditions (if comparing two areas).

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7
Q

Describe how you would carry out the quadrat practical to estimate population size of a plant species. (6 marks)

A

-Place two tape measures at right angles to form a grid over the sample area.
-Use a random number generator to select coordinates on the grid.
-Place a quadrat at each set of random coordinates.
-Count the number of chosen plant species (e.g. daisies) in each quadrat.
-Repeat the process at least 10 times to calculate a mean number per quadrat.
-Multiply the mean by the total number of quadrats that would fit in the area to estimate population size.

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8
Q

Independent Variable of the quadrat required practical

A

-The location where the quadrat is placed (e.g. sunlit vs. shaded area, or distance along a transect).

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9
Q

Dependent Variable of the quadrat required practical

A
  • The number of organisms (e.g. daisies) or the percentage cover of the species within each quadrat.
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10
Q

What is a transect?

A

-A straight line across a habitat along which samples are taken to study how the distribution of a species changes.

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11
Q

When do we use a transect instead of random sampling?

A

-When we want to see how a factor (like light, moisture, or shade) affects the distribution of organisms across a gradient.

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12
Q

How do you set up a transect?

A

-Lay a tape measure (transect line) across the area you want to study — e.g. from a path into a field.

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13
Q

How do you sample along a transect?

A

-Place quadrats at regular intervals (e.g. every 1 m) along the tape.

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14
Q

What do you record in each quadrat along the transect?

A

-The number of a specific species (e.g. daisies) or percentage cover.

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15
Q

What might you measure alongside the species distribution?

A

-An abiotic factor (e.g. light intensity, soil moisture) at each quadrat point.

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16
Q

Why do you repeat the transect in other areas?

A

-To improve reliability and identify patterns across different parts of the habitat.

17
Q

Describe how you would use a transect to investigate the effect of a factor on plant distribution. (6 marks)

A

-Place a tape measure in a straight line across the habitat you want to investigate.
-Place a quadrat at regular intervals (e.g. every 1 metre) along the line.
-In each quadrat, count the number of the plant species being studied or estimate percentage cover.
-Measure the abiotic factor at each quadrat position (e.g. light intensity using a light meter).
-Repeat the transect in different areas to improve reliability.
-Analyse how the number of organisms changes in relation to the abiotic factor across the transect.

18
Q

Independent Variable for the transect practical

A

-The distance along the transect line or environmental gradient (e.g. distance from a path or hedge).

19
Q

Dependent Variable for the transect practical

A

-The number of organisms or percentage cover of a plant species in each quadrat.

20
Q

Control Variables for the transect practical

A

-Size of the quadrat

21
Q

What is the aim of the decay required practical?

A
  • To investigate the effect of temperature on the rate of decay using milk, lipase, and phenolphthalein.
22
Q

What indicator is used and why?

A

-Phenolphthalein, which is pink in alkaline solutions and turns colourless when the pH decreases due to fatty acid release.

23
Q

What enzyme is used and what does it do?

A
  • Lipase – it breaks down lipids (fats) into fatty acids and glycerol.
24
Q

What causes the colour change in the solution?

A
  • The production of fatty acids from lipid breakdown lowers the pH, making the solution lose its pink colour.
25
What is being measured to determine the rate of decay?
-The time it takes for the pink colour to disappear.
26
Why is the solution placed in a water bath?
-To keep the reaction mixture at a specific temperature for each test.
27
Why are temperatures repeated?
-To compare how the rate of decay changes with different temperatures and identify the optimum.
28
Describe how to carry out the investigating decay practical. (6 marks)
-Label test tubes with different temperatures and set up water baths (e.g. 20°C, 30°C, 40°C, etc.). -Add 5 cm³ of lipase solution to one test tube and 5 cm³ of milk, 5 drops of phenolphthalein, and 7 cm³ of sodium carbonate to another. -Place both tubes in the same water bath and wait until they reach the target temperature. -Mix the contents of both tubes in one test tube and start the timer immediately. -Stop the timer when the solution loses its pink colour, indicating the pH has dropped. -Repeat at different temperatures and compare results to determine the effect of temperature on the rate of decay.
29
Independent Variable of the decay practical
- Temperature of the water bath.
30
Dependent Variable of the decay practical
- Time taken for the pink colour to disappear (i.e. rate of decay).
31
Control Variables of the decay practical
-Volume of lipase solution and milk solution used. -Concentration of lipase and sodium carbonate. -Volume of phenolphthalein indicator.