practical skills-mod 1 Flashcards

(16 cards)

1
Q

millimetre to micrometre to nanometre

A

mm to pm= x 1000, pm to nm= x 1000
mm to nm=x 1 000 000
nm to pm= /1000
pm to mm=/1 000 000

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

magnification equation

A

image size/actual size

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is resolution

A

ability to distinguish two separate objects, minimum distance between two objects where they can still be seen as two objects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

unit conversions

A

1m= 1000 mm
1mm= 1000 pm
1pm= 1000nm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

light microscope

A

magnify to x1000
living and dead cells
stain may be needed
resolution capped to 200nm due nature of light
wavelength of light= 400nm to 700nm
details are seen at half of wavelength, blue is shortest
colour filters used for different resolutions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

how to prepare microscope slides

A

cut thin slice of specimen using tweezers
cut with scissors to size
clean coverslip with tissue
place peel on slide
add iodine or dye using pipette
squeeze flat lightly with mounted needle, non air bubbles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

graitcule v micrometer

A

measure specimen under microscope, graticule measured in epus whereas micrometer is 10mm in total length
large division=100pm/0.1mm
small division=100pm/0.01 mm
must be calibrated
1pm=0.001mm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

two types of mounts

A

wet mount-dip with liquid to allow variety of organisms,

dry mount-observe hairs and insect parts, thin slice so light can go through, tweezers pick up specimen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

biological drawing guidance

A

-draw what is seen not diagram, add annotations, use scale, label clearly, clear continous lines, no overlapping lines, no extreme detail, use accuracy, non arrowheads, use sharp pencil, detailed title, no ruler to draw cells, protractor to draw petri dish, add scale bar (measurement1/2)
high powering=detailed, individual cells, adjacent cells, no shading

low powering=different tissue and limit boundary lines, no single cells,

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are the types of electron microscope

A

scanning/ SEM and transmitting/TEM

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

how does the TEM microscope work

A

different areas of the specimen have different thicknesses and densities, different amount of electron pass through different regions, recorded on photographic plate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

how does a SEM work

A

electron bounces off specimen, detectors pick it up and dispplays image, direction of rebound gives information on surface topography and composition

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

difference between SEM and TEM

A

transmission is 2d image, black and white, higher mag, lower res, ultrastructure

scanning is 3d image, black and white, lower mag, higher res, surface/topography

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is a disadvantage of electron microscopes

A

cannot view living cells as they use vacuums

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

effect of temperature on permability of membrane

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly