The advantage of the epidermis being clear is that the light can pass by easily without a problem. If we could not let the light pass we would have no pigmentation and that means we would have no skin tone. We would all just be really white and out pigmentation would not be there.
Answer: Animals and fungi share a common ancestor and branched away from plants at some point about 1.1 billion years ago.
Answer:
The animals present body structure is due to evolution. It is seen in each part including the structure of the heart. The vertebrate heart becomes complex from a simpler form.
Invertebrates, the heart of fishes is two-chambered having one auricle and one ventricle. The deoxygenated blood gets purified in the gills. They are aquatic and no lungs for breathing. The hearts pump a mixture of oxygenated and deoxygenated blood to the body.
The amphibians and reptiles have 3 chambered heart as they lead terrestrial mode of life. The gills modified into the lungs. The left auricle receives pure blood and the right auricle receives deoxygenated blood. The blood purified in the lungs and in the ventricle, both types of blood get a mix. The ventricle pumps the mixed-blood throughout the body.
In the case of birds and mammal, the heart is 4 chambered and the oxygenated and deoxygenated blood are separated. These two are higher vertebrates. No mix of pure and impure blood, the body receives only the oxygenated blood.
This shows to construct the phylogenetic tree of vertebrates - the fishes should be in the bottom, and above it amphibians, reptiles, then, mammals and birds on the top branch of the tree. As the chambers and structure of the hearts modified one after another.
What are your choices?
EDIT
The answer you are looking for would be wood.
Hope I helped!!
Answer: mother: XX^aa, father: X^YAa, son: X^YAa, daughter: X^X^aa.
Explanation:
Color blindness is a genetic disorder that affects the ability to distinguish colors. It is hereditary and is transmitted by an X-linked recessive allele. If a male inherits an X chromosome with the altered allele he will be color blind. In contrast, females, who have two X chromosomes, will only be colorblind if both of their X chromosomes have the altered allele. This is because <u>males have one X chromosome and one Y chromosome, while females have two X chromosomes</u>.
If the woman has normal vision, that means she cannot have both chromosomes affected. She can only have one affected chromosome (be a carrier) or none at all. Also, if she has blue eyes, which is a recessive trait, then both alleles are recessive. But the eye color is not on the X chromosome. For example, her eye color genotype can only be aa, because if she had at least one dominant allele she would have brown eye color. As for the other trait, she can be XX^, with X^ being an affected (carrier) allele or XX, i.e. both normal. So in summary, her genotype can be XXaa or XX^aa
If she has a brown-eyed male child who is also colour blind, he has inherited the allele for colour blindness from his mother, since the father does not pass on an X chromosome to the male children, only the Y. With this we can now rule out the mother's XXaa genotype since she had to have passed on her affected X^ chromosome. Then the genotype of the mother is XX^aa. And since her mother can only pass on one allele to (recessive) because she does not have allele A, the dominant that determines her brown eye color can only come from the father. So the genotype of this son is X^YAa. The female daughter has color blindness and blue eyes. So she had to inherit the affected X^ chromosome from the mother (which we already know she has) and an affected X^ chromosome from the father, because the daughter needs to inherit both affected X^ chromosomes to develop the disease. And if she also has blue eyes, she had to have inherited a recessive allele from the mother and another from the father. So with this information we can say that the father's genotype can only be X^YAa. Because the father must have both A and A alleles of the same eye color, because he passed the dominant one to the son and the recessive one to the daughter. At last, the genotype of the daughter is X^X^aa.