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As92022 L1 variation

ppt 2 sources of variation

QuestionAnswer
Variation Any difference between individuals of the same species. resulting from genetic, environmental, or combined influences.
Genetic variation The range of different alleles; allele combinations in a species or population.
Gene pool Sum of all alleles in a population
Population All members of a species in a defined area, at a specific point in time.
Environment All the abiotic and biotic factors an organism interacts with
Abiotic All the interactions an organism has with non-living things, e.g., light, temperature, nutrients etc.
biotic All the interactions an organism has with living things e.g., competition, predator/prey, parasites etc
Haploid (n) one complete set of chromosomes (n=23 in humans), e.g. sperm, egg/ova, pollen
Diploid (2n) two complete sets of chromosomes (2n=46 in humans) e.g. rest of body (somatic) cells.
Meiosis Cell division that creates 4 genetically unique haploid sex cells (gametes).
Crossing over homologous pairs exchange alleles between maternal and paternal chromatids resulting in new allele combinations in the gametes
Independent assortment Homologous pairs randomly line up either side of cell center, mixing maternal and paternal chromosomes, introducing variation into the gamete that eventually form
Segregation Alleles for a gene separate independently into different gametes. Mixes maternal and paternal alleles creating further variation in the gametes.
somatic cell all body cells except sex cells
gamete haploid sex cells e.g. sperm/egg, pollen/ova
Gonads Organ that produces the gametes e.g., testes, ovary (animals), anther, ovary (plants).
Ova Biological word for egg
Centromere Where sister chromatids of a chromosome join
Sister chromatids After DNA replication, each chromosome is made of two copies joined together, each copy is a sister chromatid.
Locus (loci plural) The location of a gene on a chromosome
Mutagen An agent that can induce or increase the frequency of mutations e.g. UV, chemicals.
Mutation A permanent random change in the DNA sequence of a gene. The only source of new alleles
somatic mutation Mutation that occurs in body (somatic) cells and are therefore not inherited, so only affects the individual within its lifetime
gametic mutation Mutation that occurs in the gamete, (sperm/egg). When fertilized the mutation/new allele is inherited by the offspring and present in every body cell.
non-heritable Is acquired after fertilization and is only present in somatic/body cells so is not passed on to offspring.
issues associated with small populations •Low genetic diversity •Lower resilience to changes in environment •Increase chance of inbreeding •More susceptible to genetic drift
Inbreeding When closely related individuals reproduce, increased chance of having the same harmful recessive alleles. Reduces fertility and genetic variation
relatedness the proportion of an organism's genes that are shared with another individual due to common ancestry. The more closely related the more alleles are shared. E.g. Parent to offspring 50%, siblings 50%
fitness a measure of an organism's ability to survive, reproduce, and pass on its genes to the next generation
genetic drift change in allele frequency due to chance. Alleles maybe lost and/or fixed by chance.
inbreeding depression The negative reproductive consequences for a population associated with having a high frequency of homozygous individuals possessing harmful recessive alleles.
non-random mating animals choose their mates. Linked to inbreeding. Increase homozygous genotypes and reduces genetic variation
Human controlled non-random mating: strategic mating human choose who mates, can choose individuals that have rare alleles/allele combinations and increase genetic variation, remove harmful alleles
migration (gene flow) Movement of alleles between populations.
immigration movement of alleles into a population: increases genetic variation by introducing new alleles or increasing the frequency of alleles
emigration movement of alleles out of a population: decreases genetic variation by removing alleles or decreasing the frequency of alleles
translocation A human controlled form of migration
natural selection phenotypes best suited to the environment survive and have greater reproductive success, passing the "successful" alleles on to their offspring
selection pressure Any factor that affects an organism survival and reproductive success.
fixed allele Only one version of the gene remains in the gene pool e.g., brown eyes only e.g. bb
Created by: NZARoberts
 

 



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