These homologous chromosomes carry different alleles of the A and B genes. How could crossing over affect the distribution of th
e four alleles: A, a, B, and b? A. Crossing over would always keep A and B together on the same chromosome, and keep a and b together on the same chromosome. B. Crossing over would always put A and B on different chromosomes, and always put a and b on different chromosomes. C. Crossing over would sometimes, but not always, exchange the positions of A and a, and of B and b, on homologous chromosomes. D. Crossing over would sometimes, but not always, delete one or more of the four alleles from both homologous chromosomes.
C. Crossing over would sometimes, but not always, exchange the positions of A and a, and of B and b, on homologous chromosomes.
Explanation:
Crossing over involves the exchange of chromosomal segments (and of course the respective genes on the chromosome segments) between non-sister chromatids in a tetrad during meiosis.
From the attached image, crossing over would sometimes exchange the positions of A and a, and that of B and b on the chromosome. However, this is not the case 100% of the time.
Crossing over. At the chiasmata during prophase I of meiosis, breakage may occur and exchange of genetic information may take place. New gene combinations which result in variations.
Independent assortment. The arrangement of homologous chromosomes at the equator of the spindle during metaphase of the first meiotic division is random. These homologous chromosomes segregate into different daughter cells which contain different genetic combinations which brings about variation
Fertilisation permits parental genes to be brought together in different combinations. This is the cause of variations in members of the same family.
Mutation is the spontaneous change in the genetic makeup of an organism. These changes may be inherited by the offspring therefore beginning variation.