bio paper 1 Flashcards

1
Q

1st step of microscopy prac

A

add drop of water to clean slide

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2
Q

step 2 of microscopy prac after adding drop of water to clean slide

A

add onion epidermal/human cheek cells on slide in water

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3
Q

3rd step of microscopy prac after adding cells onto slide

A

highlight cells using iodine stain for onion
methylene blue for cheek

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4
Q

4th step of microscopy prac after stain

A

Put cover slip on top of specimen

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5
Q

1st step of viewing cells micro prac

A

place slide onto stage and clip into place

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6
Q

2nd step of viewing cells micro prac after placing s/clipping slide on stage

A

select lowest power objective lens so lowest magnification

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7
Q

3rd step of viewing cells micro prac after choosing lowest power objective lens

A

looking in eyepiece move stage up/down using coarse adjustment knob till image becomes more focused

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8
Q

4th step of viewing cells micro prac after adjusting coarse adjustment knob

A

use fine adjustment to further focus until clear

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9
Q

5th step of viewing cells micro prac after using fine-adjustment knob

A

change to higher power objective lens and refocus if higher magnification needed

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10
Q

1st step on aseptic bacteria prac

A

pour hot agar into sterile petri dish and let set and cool

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11
Q

2nd step of aseptic prac after pouring hot agar into sterile petri dish

A

use sterile dropping pippete to evenly spread bacteria

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12
Q

3rd step of aseptic prac after using sterile dropping pippete

A

soak paper discs in diff conc of antibiotics/septics for same time and place on agar plate covered by bacteria

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13
Q

4th step of asep prac after adding paper antibiotic discs to agar

A

place disk soaked in sterile water as a control

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14
Q

5th step of asep prac after setting up water control disc

A

tape lid lightly on petri dish and incubate upside down on 48 hrs

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15
Q

1st step of osmosis prac

A

set up test tubes w 10cm3 diff conc sucrose solution with 1 pure water as control/ one 1mol/dm3

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15
Q

2nd step of osmosis prac after setting up test tubes

A

cut potato into cylinders and measure/record masses using balance

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16
Q

3rd step of osmosis prac after cutting potato into cylinders

A

put a cylinder in each beaker noting which went into which tube for 24hrs

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17
Q

step 4 of osmosis prac after putting cylinders into test tubes for 24 hrs

A

take cylinders out and dry with paper towels then rerecord mass

18
Q

1st step of amylase prac

A

place drop of iodine solution in each cavity of a spotting tile

19
Q

2nd step of amylase prac after dropping iodine in cavity

A

place test tube with 2cm3 amylase and 1cm3 of known ph buffer solution in 35 deg water bath

20
Q

3rd step of amylase prac after putting buffer/enzyme in 35 dg water bath

A

place another test tube with 2cm3 starch solution in water bath

21
Q

4th step of amylase prac

A

pour starch into amylase and buffer solution and start timer while all are in water bath

22
Q

5th step of amylase prac after mixing all solutions in water bath

A

every 10s add 1 drop of solution to iodine on spotting tile

23
Q

colour observation in amylase prac

A

blue black if starch is present
orange -brown if starch is digested to maltose

24
Q

what indicates faster rate of reaction in amylase prac

A

quicker it takes for spot to remain orange-brown

25
Q

6th step of amylase prac

A

repeat using diff ph buffers to see effect rate of starch breakdown

26
Q

how to prepare food test

A

crush food using pestle and mortar
dissolve some in distilled water
filter out any remaining solid using filter paper lined funnel

27
Q

reducing sugars step 1

A

add few drops of benedicts to test tube with food sample

28
Q

2nd step of reducing sugars test after adding benedick to sample

A

put test tube in water bath at 80 deg for 5 mins

29
Q

colour change in benedicks

A

blue—->green/yellow/brick red

30
Q

starch test

A

add few drops of iodine to sample and gently shake

31
Q

colour change in starch test

A

browny orange——>blue black

32
Q

protein test

A

add biuret solution to sample and shake

33
Q

colour change in protein test

A

blue—–>purple

34
Q

lipid test

A

add few drops of ethanol and distilled water to sample and shake

35
Q

colour change for lipid emulsion test

A

colourless—->cloudy white emulsion

36
Q

1st step of pondweed prac

A

add piece of fresh cut pondweed in boiling tube with sodium hydrogen carbonate solution

37
Q

2nd step of pondweed prac after adding it to boiling tube

A

place tube 10cm away from lamo

38
Q

3rd step of pondweed prac after placing tube 10cm away from lamp

A

switch on lamp and leave on 5 mins and count bubbles per min

39
Q

4th step in pondweed prac after switch on lamp for 5mins

A

repeat count 2x more to find mean bubbles per min

41
Q

6th step of pondweed prac after finding mean bub per min

A

repeat with boiling tube at diff distances to lamp

42
Q

how can you control temp gain from lamp in pondweed prac

A

-use led bulb
-put glass tank with water in between

43
Q

how do you get more accurate results in pondweed prac

A

collect o2 bubbles using inverted funnel and vol of gas using syringe