Agree or disagree, explain the disagrees.

the heart is composed of atria and ventricles with the atria located on the bottom and ventricles on the top of the heart.

explanation:

as blood begins to circulate, it leaves the heart from the left ventricle and goes into the aorta.

explanation:

the pulmonary artery takes blood to the lungs to pick up oxygen.

explanation:

it is not possible to get a heart transplant.

explanation:

when we inhale air, fresh oxygen goes into our blood.

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blood can travel back and forth through 2-way valves located in the heart.

explanation:

the heart is a double pump with two pumping chambers- the left and right ventricles.

explanation:

the abdomen (less formally called the belly, stomach, tummy or midriff) constitutes the part of the body between the thorax (chest) and pelvis, in humans and in other vertebrates. the region occupied by the abdomen is termed the abdominal cavity. the stomach secretes acid and enzymes that digest food. ridges of muscle tissue called rugae line the stomach. the stomach muscles contract periodically, churning food to enhance digestion. the pyloric sphincter is a muscular valve that opens to allow food to pass from the stomach to the small intestine.

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.

idk im sorry.

above statement is not a true statement about the open ocean because the open ocean has low levels of nutrients. most of the photosynthetic activity on earth occurs in the open ocean within the photic zone. organisms in the deep ocean are exposed to frigid temperatures and total darkness but it does not begin at the low-tide mark.