Workbook: Laboratory BIO32: Universiti Teknologi Mara (Uitm) Branch Sabah Campus Kota Kinabalu
Workbook: Laboratory BIO32: Universiti Teknologi Mara (Uitm) Branch Sabah Campus Kota Kinabalu
Workbook: Laboratory BIO32: Universiti Teknologi Mara (Uitm) Branch Sabah Campus Kota Kinabalu
BIO 320
FOR
LECTURER U
SE ONLY
Session Mark
Lab 1 /10
Lab 2 /20
Lab 3 /20
Lab 4 /20
Lab 5 /30
Total /100
Laboratory Session 5 (Animalia)
1. Identify two types of body forms in Cnidaria and name the parts. (5 marks)
Gastropoda
1. Most gastropods have a single,
spiraled shell and their shell can
be in conical or flattened shape.
2. Many of them have a
prominent head with eyes at the
tip of tentacles.
Bivalvia
1. Bivalves have no distinct head,
and the radula organ is lost.
2. Most of them are suspension
feeders.
Cephalopoda
1. They use their tentacles to
grasp prey and their beak-like
jaws to inject and immobilizing
poison (ink sac).
2. Sense organ and brain are well
developed.
3. Define the following terms. (5 marks)
Term Definition
Septa Structure that serves as a dividing partition or a wall in between, such as
between two tissues or between two cavities.
Hermaphroditic An organism that has both kinds of reproductive organs and can produce both
gametes associated with male and female sexes during its lifetime.
Bilateral symmetry A basic body plan in which the left and right sides of the organism can be
divided into approximate mirror images of each other along the midline.
Closed circulatory A closed circulatory system is comprised of the heart that pumps blood into
system the vessels to reach the tissues and organs. The exchange of gases in the
bloodstream occurs between smaller vessels which is capillaries and tissues.
4 pair of legs per thorax All crustaceans have 5 3 pair of legs per thorax
Number of legs pair of appendages.
Name of major sensory Pair of palps Eyes and statocysts Eyes, sensilla and ears.
organs
2) Injection/slitting:
-Lay the specimen onto a sheet of plastic or any non-absorbent
material. Then, make deep slits throughout the body of the specimen
(on main areas of focus such as muscles of the limbs, the tail, neck,
abdomen, and gaps between ribs) using a sharp blade or surgical
scalpel. Next, using a 10 or 20 cc syringe with a hypodermic needle, 10
percent formula of formalin was drawn to its full capacity and 2-5 mL
of the solution was injected each into the parts that were slitted
previously and in the abdomen and major muscles may be injected 5-
10 mL of solution. These steps are to ensure a thorough fixation and
preservation.
3) Fixation:
-This step is to arrest any decomposition and disintegration at the
cellular level, help maintain the structural integrity of the specimen
and permanently hardens the specimen. Fixation begins with
immersing the specimen completely into a large container filled with
fixative solution. Then cover the container tight to allow the fixative to
work its way for a couple of weeks (depends on size of specimen).
Along with that, the specimen was monitored to check for signs of
putrefaction.
4) Rinsing:
- After fixation, specimen was given a brief rinse using tap water to
remove the majority of the dirty formalin fixative.
6) Labelling:
- Data on name, place, date and collector’s name are enough. Use
archival acid free paper and pigment-based inks to avoid labels
becoming faded or crumpled.