0610_m17_qp_42
A paper of Biology, 0610
Questions:
6
Year:
2017
Paper:
4
Variant:
2

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Colour blindness in humans is caused by a fault in some of the light receptor cells in the retina of the eye. Rod cells and cone cells are two types of light receptor. Complete Table 3.1 to state the function of three types of cell in the eye. Table 3.1 type of cell in the eye function rod cells cone cells sensory neurones The number of rod cells and cone cells at places across the retina were recorded. The diagram of an eye in shows the angles from the fovea where the recordings were made. The graph in shows the number of rod cells and cone cells across the retina. Use to describe and explain the distribution of rod cells and cone cells across the retina. Colour blindness is a sex-linked characteristic. The gene for colour vision is on the X chromosome. There are two alleles of this gene: • B is the allele for normal colour vision • b is the allele for colour blindness. is a pedigree chart showing the inheritance of colour blindness in a family. The key shows the sex chromosomes and the alleles of the gene for colour vision. Key male with normal colour vision XBY colour-blind male XbY female with normal colour vision XBXB carrier female with normal colour vision XBXb colour-blind female XbXb Describe evidence from that shows that colour blindness is a sex-linked characteristic. A man with normal colour vision (XBY) and a woman who is colour-blind (XbXb) have a baby. Complete the genetic diagram to predict the probability that the baby is colour-blind. parental phenotypes male with normal x colour-blind female colour vision parental genotypes XBY x XbXb parental gametes offspring genotypes offspring phenotypes probability that the baby is colour-blind:
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