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Chapter 12: Variation

Form 5 Biology Bab 12: Variation

12.1 Types and Factors of Variation

  • Variation refers to differences in characteristics within the same species, even among identical twins. (p.256)
  • Variation plays an important role in evolution and forms the basis of natural selection, which allows species to adapt and survive. (p.256)
  • Variation allows species to survive environmental change, allows cross breeding to form new species, and lets natural selection keep beneficial characteristics. (p.257)
  • Continuous variation shows gradual differences from one extreme to the other, with most individuals in intermediate phenotypes, giving a bell-shaped curve. (p.258)
  • Continuous variation is quantitative, influenced by environmental factors, and examples include height, body weight and skin colour. (p.258)
  • Discontinuous variation shows distinct differences with no intermediate phenotypes, giving a bar chart. (p.259)
  • Discontinuous variation is qualitative, controlled by genetic factors and usually a single gene, and is not influenced by the environment. (p.259)
  • Examples of discontinuous variation are ability to roll tongue, eye colour and fingerprint pattern (loop, arch, whorl). (p.259)
  • About 8 to 10% of the human population has blue eyes due to low melanin in the iris. (p.259)
  • Genetic factors causing variation: crossing over, independent assortment of chromosomes, random fertilisation and mutation. (p.261)
  • Crossing over occurs between non-sister chromatids during prophase I of meiosis and produces new gene combinations. (p.261)
  • Independent assortment: during metaphase I, homologous chromosome pairs are arranged randomly, producing gametes with different combinations. (p.262)
  • Random fertilisation between sperm and egg produces zygotes with new genetic combinations. (p.262)
  • Mutation is a permanent, spontaneous change in genes or chromosomes; mutation in germ cells can be inherited, while mutation in somatic cells cannot. (p.263)
  • Environmental factors include temperature, light and soil pH; they produce environmental variation that cannot be inherited. (p.263)
  • Siamese cat fur is dark at parts with lower temperature because its pigment enzyme works only below body temperature. (p.264)
  • Hydrangea sp. produces blue flowers in acidic soil (pH below 5.5) and pink flowers in alkaline soil. (p.264)
  • Genetic and environmental factors interact; identical twins raised apart can show different phenotypes due to diet and lifestyle. (p.264)

12.2 Variation in Humans

  • Human traits are controlled by pairs of alleles; a dominant trait shows when one or two dominant alleles are present, and a recessive trait only when both alleles are recessive. (p.266)
  • Examples of dominant and recessive traits: tall/short, curly/straight hair, right/left-handed, presence/absence of dimples, free/attached earlobes. (p.266)

12.3 Mutation

  • Mutation is a spontaneous and random change in DNA. (p.269)
  • A mutagen is a substance that causes mutation or increases its rate to a dangerous level. (p.269)
  • Mutagens are physical (ultraviolet, ionising rays), chemical (carcinogens in cigarette smoke, formaldehyde, benzene) or biological (viruses, bacteria). (p.269)
  • A mutant is new genetic material produced by mutation. (p.269)
  • Gene mutation is a change in nucleotide base sequence of a gene and is also called point mutation. (p.269)
  • Gene mutation occurs by base substitution, base insertion or base deletion; it changes the amino acid sequence and the protein structure. (p.270)
  • Examples of gene mutation: sickle cell anaemia, albinism (lack of skin, hair and eye pigment), cystic fibrosis, thalassemia. (p.270)
  • Sickle cell anaemia causes red blood cells to become crescent-shaped due to abnormal haemoglobin. (p.270)
  • Chromosomal mutation changes chromosome structure or chromosome number. (p.271)
  • Types of chromosomal structural change are deletion, duplication, inversion and translocation. (p.271)
  • Nondisjunction occurs when homologous chromosomes fail to separate in anaphase I or sister chromatids fail to separate in anaphase II, producing gametes with extra or missing chromosomes. (p.272)
  • Cri du chat syndrome results from a partial deletion on the short arm of chromosome 5; affected infants have a cry similar to a meowing kitten. (p.273)
  • Jacob syndrome (44 + XYY) produces tall males with learning difficulties. (p.273)
  • Mutation in somatic cells cannot be inherited; mutation in gametes can be inherited by descendants. (p.274)
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