Module 2-The-Scientific-Self
Module 2-The-Scientific-Self
1. Mechanisms of Reproduction
2. Heredity and Behavior
3. Factors affecting an unborn child
4. Chromosomal abnormalities
Overview
This module will talk about the biological component of the self, and it
will start with the concept of reproduction. It will also cover how heredity sets
in and how it affects the person. You will gain scientific knowledge about
determining sex and the different factors that may affect the child. You will
know more about how one’s biological component will shape one’s behavior
while considering the environment.
This part of the self is scientific in nature and it is essential for you to
understand how it started and what happens as the person grow older.
Study Guide
● You can complete this module at your own phase. It means you
can take every part to study depending on your capability to do
so.
● This module starts with a brief overview about what the topic is
all about. It will also tell you the learning outcomes we would
want you to accomplish after completing this module. The
presentation of topic has complete resources you can check for
further readings and clarifications.
● Requirements involve learning activities and assessment which
are available on the last part of the module. Take time to study
each lesson carefully to apply these new learnings
appropriately.
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Learning Outcomes
Topic Presentation
It is normal for you to get curious where you came from. It is natural to
ask questions and be curious about how everything started. To attain an
understanding about such, it is important that you look at it through the
scientific lens—science of heredity. This will open the door for you to
understand more about how each one of us started our journey in the world.
THE MECHANISM OF REPRODUCTION
The beginning of human life starts with the union of two cells inside a
woman’s body. In your biology class, we had an introduction regarding the
reproductive system of both males and females. Male’s reproductive system
produces sperm cells during an intercourse and the female reproductive
system produces an egg cell every month.
During an intercourse, a man ejaculates and releases semen to a woman’s
vagina. In such ejaculation, there are around 150 million sperm cells released.
The sperm cells travel across the vagina up to the fallopian tube where the
egg cell awaits. Unfortunately, the journey is not easy for them. Around 85%
of these sperm cells are not ‘strong enough’ to travel. This leaves only
around 15% of these sperm cells capable to reach the right fallopian tube
where the egg resides. They have 12-48 hours to do this or else, they will die.
The uterus lining gets thicker every month to prepare the woman’s body for a
fertilized egg. The inner lining of the womb called endometrium prepares it. It
thickens with different layers on it. There are networks of blood vessels you
can see here. The endometrium acts as a support system as the baby grows
larger in the mother’s womb. These tissues serve as a defense system too for
the mother’s body as the embryo pushes itself more and more in the process
of pregnancy. However, when the egg is not fertilized, the endometrium with
its blood vessels falls off and that causes the menstruation.
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When the two unites, the fertilized egg is called a zygote. This egg has a total
of 46 chromosomes with equal number of chromosomes from each parent. 23
came from the mother and 23 came from the father. The chromosomes
contain chemical packets called as genes which carries the hereditary traits.
Approximately 3 days after fertilization, a 16-cell conceptus reaches the
uterus. The cells that had been loosely grouped are now compacted and look
more like a solid mass. The name given to this structure is
the morula (morula = “little mulberry”). Once inside the uterus, the conceptus
floats freely for several more days. It continues to divide, creating a ball of
approximately 100 cells, and consuming nutritive endometrial secretions
called uterine milk while the uterine lining thickens.
At this developmental stage, the conceptus is referred to as a blastocyst.
Within this structure, a group of cells forms into an inner cell mass, which is
fated to become the embryo. The cells that form the outer shell are
called trophoblasts. These cells will develop into the amniotic sac and the
fetal portion of the placenta that will provide nutrients to the unborn baby.
CELL DIVISION
During cell division, the cell undergoes two major stages called mitosis and
meiosis. In mitosis, the cell divides by duplicating Deoxyribonucleic acid
(DNA). It leads to the formation of new cells each of which has 23 pairs of
chromosomes. You started from a single embryonic cell and were
continuously growing through mitosis. Even after you were born, mitosis
continues its functions. It replaces cells through everyday hassles. The
constant replenishment of your skin comes from mitosis and it occurs all
throughout your body, keeping everything in order.
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Its body is fully formed, including ears, toes and fingers complete with
fingernails. The external genitals appeared in week 9, and now, by week 12,
have fully differentiated into male or female genitals. By week 12 the eyes
have moved to the front of the face and the eyelids remain closed together.
Fourth month
Your baby may suck its thumb now. By 14 weeks your baby will be about 9-10
cm long. Its body is now covered with a layer of fine hair called lanugo. By 16
weeks its face is becoming more
human in appearance, although the
chin is small and the mouth is quite
wide. Between 16 and 24 weeks you
should feel your baby move for the
first time — it may at first feel like
butterflies.
Fifth month
The rapid growth that your baby has
been experiencing now begins to
slow a little. By week 20 your baby
measures about 18 centimeters
from crown to rump and is half as
long as it will be when born. The
legs are now in proportion with the
body and the fingernails are well developed. Faint eyebrows are visible. At
this stage, you will feel your baby moving about a lot, often when you lie
down.
Sixth month
By 24 weeks your baby’s organs are fully formed. The baby now has the face
of a newborn baby, although the eyes are rather prominent because fat pads
are yet to build up in the baby’s cheeks. The eyelids are fused until weeks 25
to 26 when they open.
The skin is wrinkled, red and thin with little underlying fat. The skin is covered
with a waxy substance called vernix, which protects it while it is floating in the
uterus. The body is well muscled, but still thin. The baby has become better
proportioned, with the size of the body catching up with the size of the head.
Your baby’s hearing is also well developed by this stage; the baby will
respond to noise.
Seventh month
By 28 weeks lanugo hair has almost gone and hair is present on the head. Fat
is being deposited under the skin.
Eighth month
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Your baby is becoming plumper. By 30 weeks the toenails are present and by
32 weeks the fingernails have reached the ends of the fingers. The baby’s
eyes will be open when the baby’s awake.
By about 32 weeks the baby will have settled into a downward position as
there is no longer enough room left in the womb for it to move about freely.
You will feel occasional vigorous jabs of
the baby’s arms and legs.
If your baby is a boy, his testes will
migrate down into the scrotum in the 8th
month.
Ninth month
Sometime between 36 and 40 weeks,
the baby’s head will engage — that is,
the head will be lying just on top of your
cervix.
The lanugo hair that had covered your
baby has now mostly disappeared,
although some hair may remain low on
the forehead, in front of the ears and down the center of the back. The
toenails should have reached the tips of the toes.
Full term
By full-term, your baby should weigh about 2.7 to 3.5 kg, although full-term
babies can weigh anything from 2.5 to 5 kg, and measure 35 to 38
centimeters from crown to rump and 44 to 55 cm from the baby’s head to its
toes. These are just average figures, though, and there can be wide variation
in the measurements. So now, 38 weeks after conception, your baby has all
its organs and body systems ready for the big moment when it is born into the
world.
Source: https://www.mydr.com.au/babies-pregnancy/baby-s-development-in-the-
womb
You may also watch: https://topdocumentaryfilms.com/national-geographic-in-the-
womb/
SEX DETERMINATION
A normal female has XX sex cells while a normal male has XY sex cells. The
combination of XX chromosomes from both parents will result to a baby girl.
On the other hand, a pairing of XY chromosome will result to a baby boy.
MULTIPLE BIRTHS
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There are instances where a person gives birth not only to one but to two or
more child. A woman can bear two children at the same time and they are
called as twins. There are two major types of twins: Identical and Fraternal
twins.
Identical twins or monozygotic twins came from a single egg fertilized by a
single sperm cell. At some point in its fertilization process, the egg splits into
two—causing the formation of two separate identical babies. Since they came
from the same egg cell, they are mostly identical in appearance.
On the other hand, Fraternal twins came from two separate egg cells
fertilized at the same time. This will lead to the differences in the appearance,
gender, and characteristics. It is important to note that even twins are
identical, environmental influences set in which can cause differences in their
characteristics.
Occurrence of multiple births vary across the human race. It is common
among African descent and less common among European descent, and the
least common among Asians. It recurs to those families with a history of
multiple births in their generation and older mothers that are up to 40 years
old.
Source: https://www.britannica.com/science/multiple-birth#/media/1/397093/136814
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The idea of heredity came from Gregor Mendel who published his work on
pea plants in 1865. Unfortunately, his work is not widely known at that period
and was only rediscovered around 1901. Before, people assume that
Mendel’s work only accounts the big qualitative differences and the idea of
quantitative genes is not considered. It was until Ronald Aylmer Fisher
created a paper using Mendel’s pioneer study that paved the way for
scientists to realize that traits can be inherited.
Heredity is defined as the transmission of genetic traits or
characteristics from parents up to the third line of ancestry. It begins from
the moment of conception and within one’s chromosomes, genes carry traits
that are manifested by an individual.
Traits can be dominant or recessive. Dominant traits are those that are
observable while recessive traits are expressed less. Each of us receives a
pair of each trait and each of these traits can be dominant or recessive. You
can observe a dominant trait easily because it is reflected on the child’s
overall being. If a child inherits both recessive traits from the parents, it is the
only time that these recessive traits can be displayed. Knowing which other
traits you have inherited from your parents will unravel during your
development.
Here are examples of dominant and recessive traits:
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Lifestyle
Pregnant women should be mindful of their lifestyle. A pregnant woman must
take care of her body and what she takes in. Being healthy on this period
matters a lot for the baby’s health. However, some are not mindful about what
they take into their bodies such as alcohol, tobacco, and drugs.
● Alcohol- Drinking alcohol during pregnancy can increase baby’s risk
for Fetal Alcohol Spectrum Disorders (FASDs), sudden infant death
syndrome, and other related problems. FASDs have a variety of effect
to the child such as intellectual and developmental defects, behavioral
problems, abnormal facial features, and organ disorders.
https://www.healthychildren.org/SiteCollectionImagesArticleImages/FASD_Slide1_600x305.jpg
● Tobacco- Smoking during pregnancy puts the fetus at risk for preterm
birth, certain birth defects, and sudden infant death syndrome (SIDS).
One study showed that smoking doubled or even tripled the risk
of stillbirth, or fetal death after 20 weeks of pregnancy.
● Drug use- Research shows that smoking marijuana and taking drugs
during pregnancy can also harm the fetus and affect infant health. One
study showed that smoking marijuana and using illegal drugs doubled
the risk of stillbirth. Smoking marijuana during pregnancy can interfere
with normal brain development in the fetus, possibly causing long-term
problems.
Uterine blood flow
A pregnant woman experiencing an abnormal uterine blood flow has high
risk for eclampsia. This is a threatening complication that can endanger
the life of the expectant mother that can cause seizures or coma.
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CHROMOSOMAL ABNORMALITIES
Every cell in our body is composed of 23 pairs of chromosomes—a total of 46
chromosomes from both parents. The first 22 pairs are called autosomes
while the 23rd pair consists the sex chromosomes, X and Y. Females have
both X and X chromosomes while males have X and Y chromosomes. All the
information your body needs to grow and develop came from your
chromosomes. Each of these chromosomes contain thousands of genes,
which makes proteins that direct our body’s development and growth.
However, there are instances that chromosomal abnormalities occur. Such
abnormality occurs when a chromosome goes missing, switch pairing, or
there are added chromosomes from the usual count. This will result to birth
defects that can affect the brain and other parts of the body. These changes
in the chromosomes called as mutation is fatal to the embryo and at the same
time, can lead to the development of diseases.
There are different types of chromosomal abnormalities and it is important to
note that they can be categorized as numerical or structural.
Numerical abnormalities refer to the incident where a whole chromosome is
either missing from or added to the normal pair.
Structural abnormalities refer to the incident where a part of an individual’s
chromosome is missing, added, or switched to another chromosome.
These chromosomal abnormalities take place when there is an accident
during the formation of the zygote or as the cell division continues in the
development stages of the baby. The age of the mother and certain factors
may contribute in the occurrence of these genetic errors. These can cause
defects to the child depending on the specification of abnormality acquired.
Some chromosomal abnormalities lead to miscarriage, diseases, or problems
in growth and development.
chromosomes at position 21, instead of the usual pair. The disorder was first
identified in 1866 by John Langdon Down, a British physician, and later
named after him.
When a child with Trisomy 21 develops, he is at greater risk for certain
medical problems and may develop the following:
● Congenital heart disease ● Hearing loss
● Gastrointestinal abnormalities ● Speech apraxia (difficulty making
● Musculoskeletal and movement speech sounds)
problems ● Sleep disorders
● Spine disorders such as scoliosis, ● Feeding disorders
kyphosis or lordosis ● Developmental disabilities
● Endocrinologic disorders (learning disabilities, intellectual
● Epilepsy disabilities and autism)
2. Edward’s Syndrome (Trisomy 18) - Trisomy 18 is the second most
common type of trisomy syndrome, after trisomy 21. About 1 in every 5,000
babies is born with trisomy 18, and most are female. The condition is even
more common than that, but many babies with trisomy 18 don't survive past
the second or third trimester of pregnancy.
Babies with trisomy 18 are often born very small and frail. They typically have
many serious health problems and physical defects, including:
● Cleft palate ● Heart defects, including a
● Clenched fists with hole between the heart's
overlapping fingers that are upper (atrial septal defect) or
hard to straighten lower (ventricular septal
● Defects of defect) chambers
the lungs, kidneys, ● Low-set ears
and stomach/intestines ● Severe developmental
● Deformed feet (called delays
"rocker-bottom feet" ● Chest deformity
because they're shaped like ● Slowed growth
the bottom of a rocking ● Small head (microcephaly)
chair) ● Small jaw (micrognathia)
● Feeding problems ● Weak cry
3. Turner’s Syndrome- It is a condition that affects females only and results
when one of the X chromosomes is missing or partially missing. This
syndrome can cause a variety of medical problems such as short height,
failure of the ovaries to develop and heart defects.
The following signs can also be observed at birth and during infancy:
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Family members should be supportive and at the same time be able to cope
with such chromosomal aberrations that the family might encounter.
Acknowledging the problem is the first step and moving forward is the next.
Making sure that you can offer support to the young ones on these crucial
times for them would mean a lot when they grew older.
Make some more research on how you can take care of someone with these
abnormalities so you can give the best care for them. More so, know more
about their condition so you know what to watch out. Get a good support
system on these times and this also includes preparing yourself financially as
there might be complications along the way. Ask the doctor about which
helping aids you might need to create a safe and healthy environment for the
kids.
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Activity No. 1
The activity will be provided next week during your asynchronous classes.
References
Tomas, R. D., Sanchez, M. T., Paragas, E. T., Perez, N. S., Marasigan, J. B.,
Miranda, M. B., . . . Espiritu, A. F. (2018). Understanding The Self.
Malabon City: Mutya Publishing House, Inc.
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