Which choice names the two parts of earth that make up the lithosphere?

inner core and outer core

crust and outer part of the mantle

inner core and mantle

mantle and outer core

crust and outer part of the mantle

Explanation:

The lithosphere is the outermost part of the earth. It is a rocky layer, which varies in thickness in the mountainous regions and in the deep sea depths, formed by the crust (terrestrial and oceanic) and the outer part of the upper mantle.

The lithosphere (name comes from the Greek, lithos = stone, rock and sphaira = sphere) relates to the other layers, the hydrosphere, the atmosphere and the biosphere, undergoing many changes as a result of these. It is composed of minerals and rocks, which can be of three types: igneous, sedimentary and metamorphic.

Earth's layers have different chemical compositions and temperatures, which favors the mantle being more liquid because there are very high temperatures, over 1000ºC. The crust is like a film, covering the surface of the planet, it is a very solid layer, while the mantle is more "plastic", that is, has a less rigid consistency.

multiplying and dividing the two decimals and the eqations by the same number of the overalls

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.