methodology Flashcards

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1
Q

why is an insufficient number of values of independent variables e.g. 10C increase each temp, a limitation?

A

lack of results between intervals so could miss changes and be less accurate. to improve, include more intermediate ranges.

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2
Q

why is using different species for an experiment a limitation?

A

difference state may induce random error so to improve, use large sample of same organism, same species, age and size to make results more representative of population

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3
Q

what is the limitation of using a stop watch?

A

use to a greater agree of resolution e.g. 1.01s to increase accuracy

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4
Q

why is lack of control variables a limitation?

A

not confident in the effect of changing IV is causing the change in the DV, so ,method is not valid. =

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5
Q

why is choosing a piece of equipment with low resolution a limitation? e.g. measuring cylinder

A

measurements are made with high uncertainty. Therefore, using volumetric syringe.

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6
Q

how is using a piece of equipment that hasn’t been calibrated correctly a limitation?

A

introduces systematic error so increases accuracy. Therefore, must check that thermometer reads 0C degrees, and zero on all balances.

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7
Q

what is a good method to prove the IV is directly causing the change in the DV?

A

having a baseline control for comparison.

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8
Q

random error contributes to uncertainty. How can we reduce random error?

A

making more measurements and calculating mean.

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9
Q

how to increase accuracy of a practical?

A
  • take more intermediate readings
  • take more repeat readings to obtain a more accurate mean
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10
Q

list ways in which to improve confidence in findings

A
  • repeat readings
  • identify anomalies and repeat experiment to dilute the effect of anomalies.
  • calculate standard deviation (less SD, increased confidence)
  • conduct statistical test
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11
Q

how to improve validity of a practical

A
  • look for gaps in method they have not controlled e.g. pH, temp, species, conc., volume etc…
  • listing limitations of practical, and suggesting improvements e.g. thermostatically controlled water baths.
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11
Q

what are the 5 aspects of validity?

A

accuracy
precision
confidence
repeatability
reproducibility

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12
Q

what is the process of dissecting bony fish?

A
  • cut away from operculum
  • cut one gill out
  • put in water
  • stain with dye and view on microscope slide
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13
Q

what is the process of dissecting insects?

A

view spiracles with a magnifying class

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14
Q

explain the dissection of a stem

A
  • use a scalpel
  • stain xylem with methylene blue
  • see spiral lignin in microscope
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15
Q

what are the precautions you must consider when investigating transpiration rates with a potometer

A
  • healthy shoot
  • set up underwater
  • seal joints with vaseline
  • syringe to reset apparatus
  • cut bottom of stem underwater to prevent air bubbles in xylem
16
Q

ways to capture animals (biodiversity)

A
  • pit fall trap
  • mark recapture
  • tree beating
  • sweep net
  • pooter
17
Q

why must the leaves be dry in potometer?

A

to increase water potential gradient

18
Q

describe stratified sampling

A

number of samples is proportionate to each area - it ensures areas are not missed, divided strata and sample in each.

19
Q

what are two methods of systematic sampling

A

belt and line transects

20
Q

describe how to produce a cutting of a plant tissue

A
  • cut healthy shoot at an angle
  • add hormone auxin
  • water soil
  • place plastic bag over and spray with water to increase humidity
  • remove lower leaved
21
Q

describe micropropagation (tissue culture)

A
  • cut explant
  • sterilise
  • add nutrient medium + hormones
  • forms a callus = which divides to form clones
22
Q

why should a glass slide be placed over a beaker investigating chromatography?

A

to prevent evaporation of the solvent

23
Q

state the process of thin paper chromatography

A
  1. Grind up the leaves using a pestle and mortar​.
  2. Draw a line on the TLC plate with a pencil​ ​about 2cm from the bottom.
  3. place a dot of pigment in the middle of the pencil line​.
  4. allow dot to dry then add another dot over the first, repeat process until you have a concentrated pigment.
  5. add small amount of solvent 1cm from bottom.
  6. Place the TLC plate in the beaker​, with a glass over to prevent evaporation
  7. calculate rf
24
Q

the further the pigment moves up the TLC plate…

A

it is more insoluble on the chromatography paper because it’s non-polar so travels further up because it isn’t absorbed as easily

25
Q

the less the pigment moves up TLC plate…

A

the more soluble the pigment is, it is polar and is more easily absorbed onto the paper so travels slower.