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Strand 2: Structures & Processes

Reproduction

Human and plant reproduction, the menstrual cycle, pregnancy, hormonal control, contraception, fertility, and flower structure.

2.5 Human Reproduction

In brief:The human reproductive systems are adapted for gamete production, fertilisation, and development of offspring.

Male Reproductive System

Structures and functions:

  • Testes (in scrotum): produce sperm (by meiosis) and testosterone
  • Epididymis: stores and matures sperm
  • Vas deferens: tube carrying sperm from epididymis to urethra
  • Seminal vesicle: produces fructose-rich fluid to nourish sperm
  • Prostate gland: produces alkaline fluid to neutralise vaginal acidity
  • Urethra: shared tube for urine and semen
  • Penis: delivers sperm during intercourse. Glans: head of penis. Foreskin: covering of glans

Female Reproductive System

  • Ovaries: produce eggs (by meiosis) and hormones (oestrogen, progesterone)
  • Fallopian tubes (oviducts): where fertilisation occurs; transport egg to uterus via cilia and peristalsis
  • Uterus: muscular organ where the embryo implants and develops. Lined by the endometrium
  • Cervix: narrow opening between uterus and vagina
  • Vagina: birth canal and receives sperm
  • Vulva: external genitalia. Labia: protective folds. Clitoris: sensory organ

The Menstrual Cycle (28 days)

  1. Menstruation (days 1–5): uterus lining (endometrium) breaks down and is shed
  2. Follicular phase (days 1–13): FSH from pituitary stimulates follicle development in ovary. The growing follicle produces oestrogen, which rebuilds the endometrium
  3. Ovulation (day 14): surge of LH triggers release of a mature egg from the Graafian follicle
  4. Luteal phase (days 15–28): the empty follicle becomes the corpus luteum, which produces progesterone to maintain the endometrium. If no fertilisation → corpus luteum degenerates → progesterone drops → menstruation begins

Pregnancy

Fertilisation → zygotemorula (ball of cells) → blastocyst (hollow ball, implants in endometrium ~day 7) → germ layers form → embryo (weeks 3–8) → foetus (week 9 to birth)

The placenta forms to allow exchange of O₂, nutrients, and waste between mother and foetus. It also produces hormones (progesterone, oestrogen) to maintain pregnancy.

Labour and birth: Oxytocin from pituitary stimulates uterine contractions. Positive feedback loop intensifies contractions until delivery.

Hormonal Control of Reproduction

HormoneSourceRole
FSHPituitaryStimulates follicle development (female) and sperm production (male)
LHPituitaryTriggers ovulation; stimulates corpus luteum
OestrogenOvariesRebuilds endometrium; female secondary characteristics
ProgesteroneCorpus luteum/placentaMaintains endometrium; supports pregnancy
TestosteroneTestesSperm production; male secondary characteristics
OxytocinPituitaryStimulates uterine contractions during labour
ProlactinPituitaryStimulates milk production (lactation)

Contraception & Fertility

Contraception methods:

  • Natural: rhythm method, withdrawal (less reliable)
  • Mechanical: condoms, diaphragm, IUD
  • Chemical: contraceptive pill (oestrogen + progesterone prevents ovulation), morning-after pill
  • Surgical: vasectomy (males), tubal ligation (females)

Infertility treatments: stimulating ovulation (fertility drugs), artificial insemination (AI), in vitro fertilisation (IVF), intracytoplasmic sperm injection (ICSI), egg freezing.

Screening: antenatal screening (ultrasound, blood tests), genetic screening (e.g. for Down syndrome), postnatal screening (e.g. heel prick test for PKU).

Female reproductive system

Female reproductive system

Wikimedia Commons (public domain / CC)

Key Points

  • 1Male system: testes (sperm + testosterone), epididymis, vas deferens, seminal vesicle, prostate, urethra, penis.
  • 2Female system: ovaries (eggs + hormones), fallopian tubes, uterus (endometrium), cervix, vagina.
  • 3Menstrual cycle: menstruation → follicular phase (FSH, oestrogen) → ovulation (LH surge) → luteal phase (progesterone).
  • 4Pregnancy: zygote → morula → blastocyst → embryo → foetus. Placenta for exchange.
  • 5Key hormones: FSH, LH, oestrogen, progesterone, testosterone, oxytocin, prolactin.
  • 6Contraception: natural, mechanical, chemical, surgical. Fertility: IVF, ICSI, AI.
  • 7Screening: antenatal (ultrasound), genetic, postnatal (PKU heel prick test).

Learning Outcomes

  • Relate the general structure of the male and female human reproductive systems to their functions
  • Outline the phases of the menstrual cycle and the changes in hormone levels during each stage
  • Describe pregnancy from the development of fertilised zygote to birth
  • Model the role of hormones in the human male and female reproductive systems
  • Appreciate the impact of advancements in modern technology on prenatal and postnatal care
  • Discuss the use and biological implications of strategies to control fertility and treatments for infertility

Plant Reproduction

In brief:Flowering plants reproduce sexually through pollination, fertilisation, seed formation, and dispersal.

Flower Structure

Flowers contain the reproductive organs of flowering plants:

PartFunction
SepalsProtect the flower bud before it opens
PetalsAttract pollinators (insects) - often brightly coloured
Stamen (male)Anther produces pollen; filament supports the anther
Carpel (female)Stigma receives pollen; style connects to ovary containing ovules
ReceptacleBase of flower that supports all parts

Pollination

Transfer of pollen from anther to stigma.

FeatureInsect-PollinatedWind-Pollinated
PetalsLarge, colourful, scentedSmall, dull, no scent
NectarPresent (attracts insects)Absent
PollenSticky, spiky (adheres to insects)Lightweight, smooth, abundant
StigmaSticky, inside flowerFeathery, hangs outside (catches wind-blown pollen)
AnthersInside flowerDangling outside (pollen disperses in wind)

Seed Structure

  • Testa: tough outer seed coat - protects embryo
  • Embryo: the young plant, consisting of:
    • Radicle: embryonic root (first to emerge during germination)
    • Plumule: embryonic shoot (grows upward toward light)
  • Endosperm: food store for the developing embryo

Seeds produce growth regulators that stimulate growth of fruit tissues around them.

Fruit & Seed Dispersal

Seeds/fruits must be dispersed away from the parent plant to reduce competition:

  • Wind: light seeds with wings/parachutes (e.g. dandelion, sycamore)
  • Water: waterproof shells, air pockets for buoyancy (e.g. coconut)
  • Animal (external): hooks or burrs that attach to fur (e.g. burdock)
  • Animal (internal): fleshy fruits eaten, seeds pass through digestive system (e.g. blackberry)
Flower structure

Flower structure

Wikimedia Commons (public domain / CC)

Key Points

  • 1Flower parts: sepals, petals, stamen (anther + filament), carpel (stigma + style + ovary), receptacle.
  • 2Insect-pollinated: large petals, scent, nectar, sticky pollen. Wind-pollinated: small petals, feathery stigma, light pollen.
  • 3Seed structures: testa (coat), radicle (embryonic root), plumule (embryonic shoot), endosperm (food).
  • 4Seeds produce growth regulators that stimulate fruit tissue growth.
  • 5Dispersal methods: wind, water, animal (internal - eaten; external - hooks).

Learning Outcomes

  • Investigate and compare the structures of insect and wind pollinated plants and relate them to their functions, use primary and secondary data to support conclusions
  • Describe the role of seeds in plant reproduction

3. Advances in Prenatal and Postnatal Care

In brief:Modern technology allows the fetus to be monitored, conditions to be detected early, and very premature babies to survive.

Before birth

Ultrasound uses high-frequency sound waves to produce an image of the fetus, confirming the due date, checking growth and the position of the placenta, and detecting some abnormalities. It is non-invasive and carries no known risk.

Blood screening checks the mother's blood group and rhesus factor, immunity to rubella, and levels of markers that indicate raised risk of certain conditions. Anti-D injections prevent rhesus disease in later pregnancies.

Amniocentesis samples amniotic fluid containing fetal cells so chromosomes can be examined, for example to detect Down syndrome; chorionic villus sampling does the same earlier using placental tissue. Both are invasive and carry a small risk of miscarriage, so they are offered where the risk is judged high.

Non-invasive prenatal testing analyses fragments of fetal DNA in a sample of the mother's blood, giving genetic information with no risk to the pregnancy. Fetal monitoring during labour tracks the baby's heart rate, and fetal surgery can now correct some conditions before birth.

After birth

The heel prick test in the first days of life screens for conditions such as phenylketonuria, cystic fibrosis and congenital hypothyroidism, where early treatment prevents serious harm. Newborn hearing screening allows early intervention for language development.

Neonatal intensive care uses incubators for warmth, ventilators and surfactant for immature lungs, and monitored feeding, so babies born as early as 24 weeks can now survive. Vaccination programmes, developmental checks and public health nurse visits continue the care at home.

Issues to consider

These technologies improve outcomes but raise questions about the small risk of invasive tests, informed consent, and the decisions parents face after a diagnosis. Access and cost also differ between countries.

Key Points

  • 1Ultrasound: non-invasive imaging to check growth, dates and placental position
  • 2Amniocentesis and CVS examine fetal chromosomes but carry a small miscarriage risk
  • 3Non-invasive prenatal testing analyses fetal DNA in the mother's blood
  • 4Heel prick test screens newborns for conditions such as PKU and cystic fibrosis
  • 5Neonatal intensive care with incubators, ventilators and surfactant saves premature babies

Learning Outcomes

  • Appreciate the impact of advances in modern technology on prenatal and postnatal care

4. Controlling Fertility and Treating Infertility

In brief:The specification asks you to discuss both the methods used to control fertility and the treatments available for infertility.

Infertility is the inability to conceive after a year of trying. It affects roughly one couple in six, and the cause lies with either partner about equally often.

Causes

In males: low sperm number, poor sperm motility or abnormal sperm shape, or blocked tubes. In females: failure to ovulate (often hormonal, as in polycystic ovary syndrome), blocked fallopian tubes, endometriosis, or a hostile uterine environment. Age matters for both, and egg number and quality fall sharply after the mid-thirties.

Treatments

  • Hormone treatment to stimulate ovulation: drugs increase FSH activity so follicles develop and an egg is released. Risk: multiple births.
  • Artificial insemination (AI): sperm from the partner or a donor is placed directly into the uterus. Used for low sperm count or where the cervix blocks sperm.
  • In vitro fertilisation (IVF): ovulation is stimulated, eggs are collected, mixed with sperm in a dish, and one or two healthy embryos are transferred to the uterus. Used mainly for blocked fallopian tubes.
  • ICSI (intracytoplasmic sperm injection): a single sperm is injected directly into an egg. Used for severe male-factor infertility where sperm cannot penetrate the egg.
  • Egg and sperm freezing: gametes are stored in liquid nitrogen, allowing people to preserve fertility before cancer treatment or to postpone childbearing.
  • Surrogacy and donor gametes where the uterus or gametes cannot be used.

Biological and ethical implications

Treatments are expensive and emotionally demanding, success rates fall with age, hormone stimulation carries health risks, multiple pregnancies are riskier for mother and babies, and decisions about spare embryos, donor anonymity and surrogacy raise real ethical questions. Screening embryos for genetic disease before implantation helps prevent serious conditions but raises concerns about selection.

Controlling fertility

Methods are grouped as natural (avoiding intercourse near ovulation, tracked by temperature and cycle length), mechanical (condom, diaphragm, IUD; the condom is the only method that also reduces the transmission of sexually transmitted infections), chemical (the contraceptive pill, implant or injection, which supply hormones that prevent ovulation), and surgical (vasectomy or tubal ligation, effectively permanent). Each differs in reliability, reversibility, side effects and acceptability, and people choose based on health, circumstances and personal or religious beliefs.

Key Points

  • 1Infertility affects about one in six couples; causes are roughly equally male and female
  • 2Treatments: ovulation stimulation, artificial insemination, IVF, ICSI, gamete freezing
  • 3ICSI injects one sperm directly into the egg, for severe male-factor infertility
  • 4Fertility control methods are natural, mechanical, chemical or surgical
  • 5Only condoms also reduce transmission of sexually transmitted infections

Learning Outcomes

  • Discuss the use and biological implications of strategies to control fertility and treatments for infertility
  • Appreciate the impact of advancements in modern technology on prenatal and postnatal care