How does the empting of a large lake fit into the concept of the water cycle?

The emptying of a large lake fit into the concept of the water cycle because water will come back in the  form of rain

As a matter of first importance, the water from seas, lakes, streams, and so forth transforms into a gas and moves toward becoming water vapor. At that point, they ascend into the air. That is called dissipation. Next, the water vapor transforms into mists. That is called buildup. At the point when the mists are loaded up with water beads and are too overwhelming, precipitation happens and they tumble from the sky. The beads from the sky could either be rain, snow, slush, or hail. After precipitation, they experience the ground and the entire procedure begins once again once more.

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.

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