Answer: Electromagnetic waves
Explanation: The main property of the waves is the way how they propagate or travel in medium The waves which can travel without a medium is said to travel in vacuum or air.
Answer:
The correct answer is included in the Explanation section
Explanation:
An organism with considerable more chromosomes than humans: the plant <em>Ophioglossum reticulatum</em> with 1260 chromosomes.
An organism with considerable fewer chromosomes than humans: the ant <em>Myrmecia pilosula</em> with 1 chromosome.
It might be thought that the chromosome number of a species is directly related to its complexity, meaning that an organism with a large number of chromosomes is more complex than an organism with a small number. However, this is not true. Chromosomes are structures of coiled DNA, and its number indicate how the cells wrapp their genomic material when they reproduce. The number of chromosomes is not related to the organism complexity, but rather the number of genes and their function.
During a windstorm, a large old tree fell in the forest. As it came down, it trapped a young sapling about 5 meters tall underneath it. The top of the
Auxin and gibberellin in the sapling's stem will cause a gravitropic response in the sapling, and its stop will grow upward even though it is held down.
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.
