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Asexual reproduction
A single parent endows its offspring
with genes identical to its own.
– Energy efficient
– Most successful in a stable
environment
Means of asexual reproduction
Budding
– Part of the parent’s body grows and
separates from the rest of the body.
Fragmentation
– The parent’s body breaks into pieces.
– Each piece can grow into a new animal.
Parthenogenesis
– An unfertilized egg develops into an adult.
Asexual
reproduction
by budding
Sexual reproduction
• Offspring produced by fusion of two
gametes.
– Ovum (egg)
– Sperm
• A fertilized egg (zygote) forms.
• Promotes genetic variety and is
adaptive in an unstable environment.
External fertilization
Mating partners typically release eggs
and sperm into the water simultaneously.
Internal fertilization
Male delivers sperm into the female’s
body.
Hermaphroditism
Single individual produces eggs and
sperm
The primary sex organs (gonads) are those that
produce gametes (sperm and eggs).
Obtained cells Four spermatozoids from every One ovum from each oogonium
spermatogonium
Stages Growth, meiosis and maturation Follicular stage, secreting stage and
ovulation
Diagram
Spermatogenesis in the seminiferous tubules
• Penis
– Three columns of erectile tissue:
Two cavernous bodies, corpora
cavernosa.
One spongy body that surrounds the
urethra, corpus spongiosum.
– Male copulatory organ
Three stages:
• Germinal: Zygote Morula Blastocyst
• Embryonic: endoderm, mesoderm, ectoderm
• Fetal: Embryo Fetus
Differentiation
The migration of cells into three layers occurs in the 2-week-old embryo.
Stem cells
Fetus joined by the placenta
through the umbilical chord
Human birth process
• Several hormones, including estrogen,
oxytocin, and prostaglandins regulate
parturition
• Labor is divided into three stages
• Dilation of the cervix
• Fetus release: The baby is delivered during this
stage.
• Delivery of the placenta
Common sexually transmitted diseases
(STDs)
• Chlamydia
• Gonorrhea
• Syphilis
• Pelvic inflammatory disease (PID)
• Genital herpes
• HIV
Major
chemical
groups of
hormones
47, XXY (Klinefelter syndrome)
Because people with an XXY chromosome arrangement have a Y
chromosome, they are considered genetic males. Most XXY
individuals develop as males, often not knowing they have an extra
chromosome.
XXY is one of the most common genetic conditions, affecting about
1 in 660 genetic males.
Nondisjunction happens when chromosomes are distributed incorrectly during egg or sperm
formation. The gametes above either are missing or have an extra chromosome 21.
Turner Syndrome
People who have Turner syndrome develop as females.
Turner syndrome usually does not affect intelligence. Common physical
symptoms of Turner Syndrome include a stocky build, arms that turn out
slightly at the elbow, a receding lower jaw, a short webbed neck, and a
low hairline at the back of the neck.
Medical symptoms can include lymphedema (swelling of hands and
feet), heart and/or kidney defects, high blood pressure, and infertility
(inability to have children).
Hemophilia
• The hemophilia gene is carried on the
X chromosome.
• A man with hemophilia passes the
hemophilia gene to all of his
daughters, but not to his sons. His
daughters are called carriers because
they carry the hemophilia gene.
• When a carrier has a baby, there is a
one in two chance that she will pass
on the hemophilia gene. If she passes
the hemophilia gene to a son, he will
have hemophilia. If she passes the
hemophilia gene to a daughter, she will
be a carrier like her mother.
Colour blindness
• Red/green colour blindness is passed from mother to son on the
23rd chromosome.
• If you are colour blind it means the instructions for the
development of your cone cells are faulty and the cone cells
might be missing, or less sensitive to light or it may be that the
pathway from your cone cells to your brain has not developed
correctly.
• The faulty ‘gene’ for colour blindness is found only on the X
chromosome. So, for a male to be colour blind the faulty colour
blindness ‘gene’ only has to appear on his X chromosome. For a
female to be colour blind it must be present on both of her X
chromosomes. This is why red/green colour blindness is far
more common in men than women.
• Blue colour blindness affects both men and women equally,
because it is carried on a non-sex chromosome.