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Question: How does the behavior of chromosomes during meiosis generate variation
Genetic variation is introduced during meiosis in a few ways: 1. Independent Assortment: This relates to the way in which chromosomes line up during meiosis. Each pair of chromosomes (one from the mother and one from the father) lines up on the metaphase plate during Meiosis I independent of other pairs. So there is a 50:50 chance, for any given pair, which homologue (the one from mom or the one from dad) ends up in each resulting gamete. Given that humans, for example, have 23 pairs of chromosomes, this can lead to 2^23 (roughly 8 million) different combinations of chromosomes in gametes! This is a significant source of genetic variation. 2. Crossing Over: This occurs during Prophase I of meiosis, when homologous chromosomes pair up. The chromosomes physically break and exchange sections, leading to chromosomes that are a mix of alleles from both the mother and the father. This can lead to new combinations of traits that were not present in either parent, creating more variability in the population. 3. Random Fertilization: Basically, which particular sperm fertilizes which particular egg is pretty random. Given the amount of variation produced in gametes due to independent assortment and crossing over, this leads to a huge potential variety in the genetic makeup of the offspring. Together, these processes introduce large amounts of variation, forming the basis for evolution guided by natural selection.
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