At one time, all living organisms were separated into only two kingdoms—Animals and Vegetables. Once the microscope was invented and improvements in microscopy were made, however, more kingdoms were defined. The Protist kingdom was established in 1866, and the Monera kingdom was added in 1938. The Monera kingdom was later subdivided into the Bacteria and Archaea kingdoms in the 1990s. Fungi were classified as plants until 1969. What is one reason why fungi were separated into a new kingdom? A. Fungi are able to undergo photosynthesis and make their own food. Plants get the nutrients that they need by consuming other organisms. B. Fungi are prokaryotic. Plants are eukaryotic. C. The cell walls in fungi are composed of chitin. Plant cell walls are composed of cellulose. D. All fungi are unicellular. All plants are multicellular.

i don’t no. suiopgohjk

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.

a covalent bond, specfically triple bond