Answer:
Certainly more than that.
Explanation:
Answer:
enable capillarity
Explanation:
It is well known that water tends to adhere to the walls of the vessel in which it is contained. This is due to the force of adhesion which is defined as the force of attraction between unlike molecules. Cohesion is defined as the force of attraction between like molecules. In the case of a plant, cohesion of water molecules in the xylem vessels prevents the water column from breaking. The forces of adhesion, surface tension and cohesion are the basis of capillarity,that is, the rise of liquids in capillary tubes.
Answer: skull size of each species
Over time, it is the size of the skull particulary that of the jaw bones, that can help determine the evolutionary relationship of two hominid species. It was believed that the jaws of hominids change as time passes by because the size of the brains changes too.
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.
Answer:
The correct answer is <em>B. False</em>
Explanation:
<em>The genotype of an organism determines its phenotype</em>. Phenotype is constituted by observable characteristics of an organism. These characteristics are codified by genes, and the combination of the differents variants of a gene which codify a phenotipic characteristic constitutes the genotype. For example: eyes color is a characteristic. Its is codified by variants of a gene. The combination of two variants of a gene gives a genotype, which codifies for the phenotype 'blue eyes'.
