Termites eat wood, but many do not produce enzymes themselves that will digest the cellulose in the wood. Instead, some termites house a complex community of protozoa, bacteria, and archaea that could help digest the cellulose. Imagine an experiment that fed termites either wood only or wood and antibiotics, and then measured the amount of energy extracted from the wood. If both groups gained equal amounts of energy, which of the conclusions is the most logical?a) We would conclude that the archaea contributed to digestion of cellulose and lignin.
b) We would conclude that the bacteria did not contribute to digestion of cellulose and lignin.
c) We would conclude that none of the three groups were needed to digest cellulose and lignin.
d) We would conclude that the protozoa contributed to digestion of cellulose and lignin.

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.

answer: pee on jews

explanation: