Why would a group of small cells help an organisms maintain homeostasis better than one large cell

Because the group of small cells would have a greater surface area-to-volume ratio, so they are able to exchange materials with their surroundings more efficiently.

Explanation:

ANSWER ISDRUM ROLL PLZ

A group of small cells help an organism to maintain the homeostasis better than the large ones because the smaller cells can maximize the ratio of surface area to volume. The more will the ratio more will be the exchange of ions and molecules across the cell membrane per unit cytoplasm. The basal metabolic rate of smaller cells is much higher to that of bigger ones. The higher the metabolic rate the better is the maintenance of homeostasis.

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BRAINLIEST PLZ

Explanation:

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.