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RATIFICATION PAGE
Complete report of general Biology which title “how to use microscope” was
made by:
Name : Syahril
Reg. No : 101204156
Group/Class : II/ICP
Department : Physics
After checked by assistant and assistant coordinator so this report is
accepted
Makassar, 10th November
2010
Assistant Coordinator
Djumariranto S.pd
Assistant
Nursyahraeni Malik
CHAPTER I
INTRODUCTION
A.Background
One of the important senses for the human is eyes, its function for see
anything. Human without eyes are very queer. That’s why we need it, but our
eyes has limitation for seeing. Bacteria and virus can’t saw by our eyes. In
addition to this, we need a media for see a small object. Of course to help our eyes
to identify and clarification an object. The first we know about LUV (it always
called maximize mirror) but still many problem for seeing more small object. On
develop of science and technology, we know about microscope. It can use for
identify and clarification for the small object
In the field of science, microscope has an important role to support it. Not
only for biology but also the others such as: physics, chemistry, astronomy, etc.
The different side of LUV and microscope is LUV still has limitation for seeing
the small object. Microscope more strong than LUV because it have two lens that
can maximize a shadow object from preparation more than 100x.
In generally, microscope divide for two parts. They are optical microscope
and electron microscope. Optical microscope have two lens (ocular lens and
objective lens). Both of these lens used to maximize an object. Objective lens is
used to maximize an object from preparation place and continued the shadow
from preparation to ocular lens. Objective lens can maximize the shadow of an
object more than 10 x 1500 x. And ocular lens is a lens that its place near with our
eyes, its function is to maximize the shadow of an object from objective lens. The
other one is electron microscope. a scientific instrument which is used to magnify
things on a fine scale. That uses a particle beam of electrons to illuminate a
specimen and create a highly-magnified image. Electron microscopes have much
greater resolving power than light microscopes that use electromagnetic radiation
and can obtain much higher magnifications of up to 1 million times, while the best
light microscopes are limited to magnifications of 1000 times. Both electron and
light microscopes have resolution limitations, imposed by the wavelength of the
radiation they use. The greater resolution and magnification of the electron
microscope is because the de Broglie wavelength of an electron is much smaller
than that of a photon of visible light. The electron microscope uses electrostatic
and electromagnetic lenses in forming the image by controlling the electron beam
to focus it at a specific plane relative to the specimen. This manner is similar to
how a light microscope uses glass lenses to focus light on or through a specimen
to form an image. In addition, electron microscope can maximize the shadow of
an object more than 1, 5 billion.
From this view above, we must know about microscope. And as the
students its very important to increase our knowledge in science, specially
biology.
B. Purpose
1. Give the students knowledge about how to use the microscope safely and quickly
2. Give the students knowledge about the part of microscope3. Give the students knowledge about an observation concept, specially cell
of plants4. Give the students knowledge about kinds of microscope
C. Benefit
After the student do this experiment, they have skills about how to use
microscope correctly, quickly and peacefully to see a simple preparation of an
object such as cell of plants, etc. the students know the part of microscope, and
they know the characteristic of optical microscope and electron microscope
CHAPTER II
PREVIEW AND LITERATURE
Microscope is a major toll in studying the structure of small objects.
Microscope that user light called an optical microscope, which is widely used in
school laboratory. Optical microscope can be differentiated into on monocular
biology microscope and stereo microscope or binoculars. Biology microscope
used for observation of thin transparent objects. Radiation is given from below
with natural light or lamp. In this biology microscope, generally have ocular lens
and objective lens, while binocular or stereo microscope is used for observation of
objects that are not too large, transparent or not. Radiator can be set from above
or from bellow with natural light or lamp. Has two objectives and two eyepiece,
so the three dimensional obtained with the two martial eye observation. (Team
Teaching, 2010 )
A microscope may be defined as an optical instrument,consisting of a lens
or combination of lenses, for making enlarged or magnified images of minute
objects. A simple microscope, or a single microscope , consist merely of a single
lens or magnifiying glass hell in aframe,usually adjustable, and often provided
with astand for conveniently holding the object to be viewed and a mirror for one
in that it consists of two sets of lenses, one known as an objektive and the other
as an eyepieces,commonly mounted in a holder know as a body tube. The one
neares the specimen, called the objective, magnifies the specimen a definite
amoun. The second lens system, the eyepiece, further magnifies the image formed
by the objective, so thet the image seen by the eye has a magnification equal to the
product of the magnification of the two systems. The individual or initial
magnification of the objectives and eyepieces is egraved on each such part.
Accurate focusing is attained by a special screw appliance know as a fine
adjustment. Compound microscopes give much greater magnification than simpel
microscopes and are necessary for viewing and examining such minute objects as
bacteria. (Salle, 1961)
A microscope is a tool or machine with the ability to increase the vicual
size of an object so thet it is easier to see. All types of microscope must perfom
two important function; they must magnifi (enlerge) the specimen to a size that
can be seen by the human eye, and they must provide a clear image thet will
enable the microscopist to distinguisth the component parts of the specimen, a
feature known as resolution. Those may be accomplished by using visible (white)
light, ultraviolet light, or electron beams.(Ross,1986)
Microscope which is first applied by saintis Renaisans, as well as which
we apply d laboratory is light microscope. Visible light is overcome [by] through
object and then pierces this kacaLensa lens refraction of light sedemikisan aspect
so that object shadow dipebesar at the time is projected to our eye.
Two important values a microscope is magnification power and dispertion,
or resolution express how many times big object is seen with microscope
compared to measure sebenarnnya..Daya decompose is clarity measure of image
that is distance a minimum of two detachable points and admits of differentiated
as two separate points.( Campell, 2008 )
Generally, the microscope has a magnification power as follows:
• Objective 4X and 10X ocular, 40X total zoom
• Objective 10X and 10X eyepiece, the total magnification 100x
• Objective 40X and 10X eyepiece, the total magnification 400x
• 100x objective and 10X eyepiece, the total magnification 1000x
Objective of the most powerful in the optical microscope objective emersi
100x called because of its use must be with emersi oil, and how to use it
must be special as well.
According to Goldstein (2002) section on the microscope to divide into 3
categories
A. Optical section. This section of the lens. The lens can zoom in or out of
the shadow of a shadow object. In addition it also describes the
shadow of the object lens.
B. The part that relates to illumination. That is part of the microscope that
requires lighting. Some mikrosko is equipped with a lamp which sends
light into the body through a microscope while the other microscope
equipped with a mirror that can be moved to get a natural or artificial
light and then reflect into your eyes.
C. Mechanical parts. This section provides convenience and comfort in
the use of a microscope. There is a motion platform which is a pillar
Roller Stay upright, arms arch, and the pulpit called the stage. In the
microscope there is also a useful link inclination to tilt the microscope
at the appropriate angle for facebook to observe comfortably. Optical
microscope is a microscope basically optical lens. Expert science
related development with optical microscope was Anton Van
Leuwennhoek.
.
CHAPTER III
PRACTICUM METHOD
A. Day and date
Day/Date : Wednesday,3rd November 2010
Time : 09.00-10.00 am
Place : General Biology Laboratory at second floor east.
Faculty mathematics and science
Makassar State University
B. Tools and materials
1. Tools
There is tool even that is utilized this on liking is which is:
1. Tools that provided by laboratory
A. Biology microscope
B. Toolbox, contain:
1. Object glass
2. Cover glass
3. Petri dish
4. Pincers
5. Pipette hand
2. Tool that provided by college student
a. New knife
b. Flannel's cloth new
c. Cotton mop
d. Pictured book and penciled
\ e. Toothpick
2. Materials
There is material even of this attempt which is:
1. Material that provided by laboratory
a. Distilled water
b. Filter paper or blotting paper
c. Cotton or kapok
2. Material that provided by college student
a. Hibiscus leaf (Hibiscus rosa sinensis)
b. waru's leaf (Hibiscus tiliaceus)
c. Gourd leaf (Cucurbita moschata)
d. Red onion (Alium cepa)
C. Work and procedure
1. Preparing Microscope
a. Placing microscope upon dihapan's correct workbench.
b. Clearing microscope body with pane cloth. Don't on and off rub
lens with cloth.
c. Opening instrumental box, put for meaty solder cup object glass
and shell glass. Clearing object cloth with cotton or filter paper
cloth.
d. Upon workbench there's only microscope, instrumental box with
its content, guidebook and note, materials for practicum. Keep
away that another on other place already been provided.
2. Managing its Light Input into Tubus
2.1. Paying attention pracicum's room situation, where is its
coming aim light which more brightness (of front, left, or right)
then leads microscope mirror go to that light source and opens
diaphragm or turn around plate on course hole be. Managing
microscope position that has condensor to approach sediaan's table
wields monotonic mirror. For microscope without kondensor
utilize concave mirror.
2.2. Managing revolver position so objects hortesting to had up
to sediaan's table until click sound.
2.3. Downing tubus until objektif's tip distance with sediaan's
table 5 10 mm or tube is down maximal.
2.4. Telescoped lens ocular by left wink without squinting
right eye (need training) will in view white domed field (field of
view). If its brightness don't merata, therefore we move few
reflecting until its brightness rolled out. If over dazzle, we narrow
diaphragm or hole on plate. If field of view is still elope incoming
light reducing matter, therefore we open diaphragm, hole tide is
even greater on plate.
2.5. Ready microscope to be used observesobject.
3. Trick Spaces Lens with object
3.1. Turning around or makrometer's crude regulator towards
finger smith, tubus goes down, objektif's distance with sediaan
mengecil's table, then contrariwise. What happen? Other model
microscope tubusnya's one coves or can't fluctuate, therefore table
sediaan moves up and down if turn around makrometer and
micrometer.
3.2. Put together meaty object glass upon object's table in such
a way face so observed material lies in the middle table hole,
nipping object glass with sengkeling so not rock.
3.3. objektif's distance with object glass no more than 10 mm.
If that distance is oversized, therefore we turn around makrometer
to down tubus while seeing from objektif's tip side approach object
glass until a maximum 5 10 mm.
3.4. look passes okuler while hand turns around makrometer
raises tubus slow. Observing field of view until shadow
appearance, if tubus was lifted half-turn makrometer was emerging
shadow, matter most overlooks, therefore we go over to step 3.3
backs, if have available shadow but still blur, therefore us
meneropong goes on while turn around rise micrometer or
downwards until shadow be clear line or its limitation.
3.5. Checking lens ocular's magnification and objektif and that
shadow magnification.
3.6. Issuing preparat already being observed. .
4. Substituting magnification
4.1. If watch was successful, 3. 4 and 3.5, seeming shadow will
be raised again and doesn't touch preparat's position or tube.
4.2. Turn around in such a way objektif's face until lens that
longer (heavy duty) upright on sediaan's table and click sound
(check magnification)
4.3. Meneropong while turns around micrometer until greater
shadow appearance of observed shadow.
4.4. If baffled finds greater shadow, we raise tubus by turns
around makrometer contrary aims finger smith, turning around
revolver backing to place objektif's lens position rans down (short)
on course originally without change preparat's position then
mengulang again stage 3.3, 3. 4, 3. 5 lanjut goes to 5.1, 5. 2, 5. 3,
until successful.
4.5. Raising tubus if will observe material any other and issues
preparat already been observed then clears object glass and shell
glass.
4.6. Making new sediaan appropriate staged new 4.1 until 4.6.
4.7. At the early activity which utilize microscope, notice
following things:
i. Preparat may not above keep sediaan's table but we shall
issue it.
ii. Clearing wet preparat with filter paper or cotton mop
(object glass + closing glass) then keeps it in solder cup and
inserts it into outfit box.
iii. Clearing microscope body with pane cloth, downing tubus
as low as maybe.
iv. Keeping microscope into microscope box.
v. Clear all equipment has already used by cotton mop and is
kept deep its box.
vi. Keep alone instrumental already been taken in for next
activity.
vii. Discarding material rest that doesn't be utilized again at
available garbage can.
CHAPTER IV
RESULT DISCUSSION
A. Result
Plant Picture
Daun waru (Hibiscus tilaceus)
Daun labu (Cucurbita muschata)
Bawang merah (Allium cepa)
Daun bunga kembang sepatu (Hibiscus rosa-
sinensis)
B. Discussion
Based on the results, we can determine the shape and structure of the
preparations were observed, including:
1. Red onion (alium cepa)
The observed part of the tuber onion is cut crosswise, then taken the
very thin using a razor blade, then placed on the object.
Furthermore, red onion observe by using the magnification of 10 x 10
is visible is the structure that looks like stone structure which coincides
with each other each other. Where in the margins of this structure is
called the epidermis while surrounded by the NII is the cytoplasm and
cell wall in the middle of the cell nucleus contained cytoplasm..
2. Leaves of hibiscus (hibiscus teliaceus)
From the observation hibiscus leaves, especially the bottom of the leaf
turns out we have a star-shaped trichomes. These include the type of
trichome trichomes which produce no secret, at this star hair cells have
followed Kula. In this case the outer wall of the respective hair cell
head slowly swell and spread, forming a layer of mucus that resembles
Cuba under Kula followed.
3. Leaves of hibiscus (hibiscus rosasinensis)
The third observation is the hibiscus, the part that was observed on
hibiscus in transversely sliced as thinly as possible using a razor blade.
Having put the slices on the counter preparations, pot observation with
perbesaraan 10 x 10 and the results are immediately visible, terdapt
boxes that coincide with each other each other.
4. Leaves of pumpkin (Cucurbita moschata)
Part of the observed is that the leaf edges with a thin slice through the
most thin sections using a razor blade and then put it over the object.
The image is the image that his model looks like a needle, in which
one end is greater as there are bars or how the joints
The components of the optical microscope is shown in Figure consists of an
optical microscope.
1. Foot microscope, as the pedestal base stand.
2. Pole, where the jointed arm microscope, or grip with the axis inklinai
3. Arm or hand microscope, which is held when appointed.
4. Mirror, a tool catcher and reflective
5. Regulatory condenser, when rotated to raise or lower the condenser
6. Condenser, a lens that collects light beam from the mirror into a hole
preparation table.
7. The diaphragm, a tool that can be closed and opened, the regulator of the
amount of light entering the condenser.
8. Preparation table, where lay the glass objects (glass objects).
9. Sengkeling, clamp or regulator where the dosage (glass objects)
10. Mechanical mover, appliance control objects on a table where the glass
11. Hole preparation table, a hole in the middle of the table supplies the
passage of light from the condenser where the entrance to the object glass
lens continues to objektif
12. Makrometer, coarse regulator, homing tubus up or down smoothly.
13. Micrometers, roughly regulator, homing tubus up or down smoothly.
14. Tube or ocular tabling, at its top end there are ocular lenses.
15. Revolver or objective player, disk space, rnelekatnya objective lens of
various sizes.
16. Objective lenses, which function is facing perpendicular to the table
inventory, receive inventory and then raised her shadow.
17. Ocular lens, which spy the eye of the observer, accept the shadow of the
objective and raised.
CHAPTER V
CONCLUSION AND SUGGESTION
A. Conclussion
According this research, i conclude if microscope is tool that help us to
look an object that microscopic. This a fantastic matter, especially in science
and technology. To use this tool, need the true method to know part of
microscope, ingridients to clean, etc. So, when look a preparat can look well.
B.Suggestion
- For Assistan
Comunication between the practican and assistant more increase
- For Laboratory
Practicum tools which use very limitation until the observe can not it
worked maximal. -Because that it hoped in order that numbering tool
practicum in enough
BIBLIOGRAFI
From wapedia. Light microscope. www.google.com. Accessed on 3 November
2010.
From Wikipedia Bahasa Indonesian, the free encyclopaedia. www.google.com.
Accessed on 3 November 2010.
Cambell, Neil. 2008. Biologi edisi 5. Jakarta: Erlangga
Ross,Fredrick. 1986. Introductory mikrobiology. Illinois: Scott Foresman and
Company
Salle.1961. Fundamental principles of bacteriology. New York: McGraw-Hill
Book Company
Tim Pengajar.2010. penuntun praktikum biologi dasar.Makassar
APPENDIX
Answering Questions;
1. Write the name of the optics of the microscope!
Answer:
a. Mirror
b. Condenser
c. Ocular lens
d. Objective Lens
2. Write the name of the mechanical parts of the microscope!
Answer:
a. Leg microscop
b. Pole
c. Microscope lens
d. Rengatur condenser
e. Diaphragm
f. Preparation table
g. Sengkeling
h. Mechanical activator
i. Hole preparation table
j. Makrometer
k. Micrometer.
l. Tubus
m. Revolve
3. Write the function of mechanical parts !
Answer :
a. Tubus (reed binoculars) as a place to attach the lens
b. Revolver is to put the lens - ocular lens.
c. Stem or handle of a supporter of binoculars and as a place to grip when
mickroscope lifted.
d. Object table as a place to put the preparations to be examined.
e. Screws activator preparations (mechanical drive) to swap the object glass
f. Coarse screw (makrometer) to regulate and lower the microscope
following ascending magnifying lens.
g. Screws fine (micrometer), to regulate the body slowly - to obtain a shadow
land of sharp objects.
h. Regulatory condenser serves to move the condenser up and down.
i. Pole that connects the foot with handle.
j. Leg or pedestal is the base of the microscope to give stability to the
microscope.
k. Sengkeling, clamp or regulator where the dosage so as not to shift.
l. Hole preparation table, as the passage of light from the condenser into the
glass object and then to the objective lens.
m. Ring filter to filter the incoming light.
4. If the image in the field of view will be shifted to the left front, toward where
the glass objects / dosage should be shifted? why is that?
Answer:
Glass objects should be shifted to the right-back because of the reflection of light
at the concave mirror that will produce a shadow enlarged or reversed.
5. Write a negative effect on the microscope when the lens was rubbed with a
cloth or plain paper / rough
Answer:
a. Can damage the existing lens on the microscope
b. Damaged or scratched lens can not produce good images