5. what is the evolutionary relationship among archaea, bacteria, and eukarya?
a. since archaea are the most primitive, archaean ancestors gave rise to bacteria
that in turn gave rise to eukaryotes.
b. all three domains are equally distant from the most primitive common ancestor,
a protocell.
c. archaea and eukarya share nucleic acid similarities so eukarya split off from
archaea.
d. bacterial ancestors gave rise to both archaea and to eukaryotes as two
separate side branches.
e. archaea ancestors gave rise to both bacteria and to eukaryotes as two separate
side branches.

4

ans.

gregor john mendel is known for study of inheritance in pea plants. he used garden pea plant for his study, having alternative traits for various characters. he performed cross-breeding in pea plants to check how characters are transmitted between parents to offspring, such as cross between pure tall and pure dwarf plant. mendel studied the inheritance patterns in pea plants for various generations.

thus, the correct answer includes options and f).

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.