EXPT: 1
DATE:18-6-24
TEMPORARY MOUNT OF A LEAF PEEL
Aim
To prepare a temporary mount of a leaf peel in order
to show the stomata of a leaf.
Material Required
     A potted plant of Bryophyllum or Tradescantia
     Needles
     Forceps
     Watch glass
     Dropper
     Glass slides
     A brush
     Coverslips
     Blotting paper
     Safranin
     Compound microscope
     Glycerine
Procedure
    Pick a healthy leaf from the potted plant
    Fold the leaf to gently pull the peel apart to separate a
     peeled section from the lower surface of the leaf. Use
     the forceps to perform this step. Allow the peel to
     remain in a watch glass holding water for some time.
    In the watch glass, stain the sample by adding some
     drops of safranin through a dropper.
    Take the peel out after 2-3 minutes. Set it on a clear
     glass slide
    Add a drop of glycerin on the peel. Put a clear
     coverslip over it gently using a needle.
    Excess glycerin and stain can be removed using
     blotting paper
    Examine the slide first under a low-power and then
     under a high-power magnification of a compound
     microscope.
Diagram
Observation
    Visible epidermal cells. The cells in their outline are
     irregular with no intercellular spaces
     Small openings, stomata are scattered through the
      epidermal cells
     Guard cells are observed which have chloroplasts and
      nucleus
     Guard cells are observed having a thin outer covering
      and a thick inner boundary(concave)
     Guard cells control the closing and opening of the
      stomata.
Conclusions
Epidermal cells are found containing stomata on the
lower surfaces of the leaf.
EXPT:2
DATE:11-7-24
                RESPIRATION
Aim
To experimentally demonstrate that carbon dioxide
is released during the process of respiration.
Material Required
    Soaked gram seeds
    U-shaped delivery tube
    Conical flask
    Blotting paper (moist) /cotton wool
    Thread
    Water
    Beaker
    Test tube
    Rubber cork with a single hole
    Freshly prepared KOH solution (20%)
    Vaseline
Procedure
    Germinate close to 25 seeds. This can be done by
     wrapping them in moist blotting paper or cotton wool
     for around 3 to 4 days.
    Set up the germinated or sprouted seeds in the conical
     flask. Spray some water into the flask to dampen the
     seeds.
    With the help of a thread, suspend the conical flask
     containing the test tube having a freshly prepared
     20% KOH solution.
    Use the rubber cork to seal the opening of the conical
     flask.
    One edge of the U-shaped glass delivery tube present
     in the conical flask should be inserted through the
     hole in the rubber cork. The other edge should be
     placed into a beaker that is saturated with water.
    All attachments of the set-up should be sealed. This
     can be done using vaseline to create an air-tight
     environment.
    The initial water level present in the U-shaped
     delivery tube needs to be marked.
    Leave the experimental set-up uninterrupted for 1 to
     2 hours. Observe the fluctuations in the water level in
     the tube.
Observation
Careful observation after a certain period of time
reveals that the water level in the U-shaped delivery
tube has risen in the beaker.
Conclusions
The rise in level water indicates that carbon dioxide
is released as a result of germinating gram seeds
during the process of respiration in the conical flask.
The carbon dioxide that is released in the process is
absorbed or consumed by the KOH solution that is
suspended in the test tube in the conical flask,
creating a vacuum or a void in the flask resulting in
the upward water movement in the tube. Hence, the
water level in the tube changes.
EXPT NO.3
DATE:12-8-24
           STUDY OF PREPARED SLIDES
Aim
To study about (a) Binary Fission in amoeba and (b)
Budding in yeast with the help of prepared slides
Material Required
     Compound microscope
     Permanent slides of budding in yeast and binary fission in
      amoeba
Procedure
     Place the slide under a compound microscope
     Focus the slide, first under low power and later under high
      power of the compound microscope
     Various stages of budding and binary fission can be
      carefully examined
Observation
(a) Binary fission in Amoeba
     Initially, the pseudopodia are retrieved. The body of
      amoeba is coiled and becomes round
     Amitosis is observed, the division of the nucleus takes
      places which are followed by splitting of cytoplasm
     At the point of fission in the body of the amoeba, a
      constriction starts to develop.
     The constriction or furrow turns deeper resulting in the
      formation of two daughter cells
(b) Budding in yeast
     Protuberance or a tiny outgrowth is observed on the parent
      cell
     Division of the nucleus is observed which is later seen in
      the bud
     Repetitive budding leads to the formation of a chain of cells
Conclusions:
The prepared slides display asexual reproduction. One
individual is involved to produce a new offspring of its
own kind.
     Slides need to be aligned and focused accurately
     Sketch out your observation that is observed under a
      microscope
     The slides first need to be examined under a low-power
      magnification of the compound microscope and then under
      high-power magnification.
EXPT NO.4
DATE:29-8-24
PARTS OF AN EMBRYO-DICOT SEED
Aim
To identify the different parts of an embryo of a
dicot seed
Material Required
     Seeds of red kidney bean/gram
     Forceps
     Magnifying glass
     Cloth
     Petri dish
     Water
Procedure
     Soak a few seeds overnight
     Next morning, drain the excess water out
     Now wrap the seeds in a clean and a moist cloth for a day,
      allow it to dry
     Next, carefully peel the seed coat
     With the help of forceps, dissect the seed so as to get two
      equal halves
     Examine with the help of a magnifying glass. Carefully
      identify and locate different parts of the seed
    Sketch out the interior of the seed you examined labeling
     all the parts as shown in the diagram.
Diagram
Observation
    The bean seed resembles the shape of a kidney. It has a
     convex and a concave side
    A scar known as the hilum is observed on the slightly
     darker side of the concave side
    A tiny pore known as the micropyle is located just adjacent
     to the hilum
    The seed is enclosed by a seed coat
    The embryo possesses two distinct and large cotyledons
     that resemble the shape of a kidney and are white in color
    Lateral attachment of the cotyledons to the curved
     embryonal axis is observed
     Radicle is examined. It is the rod-shaped and lightly
      protrusive lower end of the embryonal axis that is found
      placed towards the micropylar end.
     The upper end of the embryonal axis exhibits the plumule
     Hypocotyl is observed which is a section of the embryo
      axis found in between the radicle and adjunct of cotyledon
      leaves
     The epicotyl is also observed which is the section of the
      embryo axis between the adjunct of cotyledon leaves and
      plumule
Conclusion
Three principle parts of the embryo of dicot seeds
are observed, they are:
     Cotyledons
     Plumule
     Radicle