Which options identify the main ocean zones? check all that apply.
deep
intertidal
neritic
open-ocean
surface

The options that identify the main ocean zones are intertidal

, neritic

, open-ocean.

Explanation:

The nutrients that are present in the water and the quantity of light form that is reaching the water varies form one location to another. The distance of the ocean from the shore and the depth of the water are the deciding factors of the above mentioned things.

Apart from these things ocean has three main zones which are intertidal

, neritic

, open-oceanic zone. Another type of zone is formed by the ocean floor. The presence of nutrients in the water is decided by the measure of distance of the ocean form the shore. The water that lies very close to the shore will be having more nutrients that the water away from the shore.  

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.