What is a major challenge of current space exploration?
a. developing bigger rockets
b. setting a clear goal for the future
c. sending unmanned probes to other planets
d. securing international cooperation for missions

B) Setting a clear goal for the future.

Explanation:

At this point in time, the future of space exploration is unclear. NASA is debating whether we should return to the Moon, or press on to Mars. (although it seems more likely that we will go to Mars some time in the future.)

(I took the quiz, and it was right.)

correct answer is option a.

tropopause, stratopause and mesopause have all in common aspect that is point of maximum temperature in its layer of the atmosphere. all layers of atmosphere observe abrupt change in temperature. tropopause is the boundary between troposphere and stratosphere. stratopause is the boundary between stratosphere and mesosphere. mesopause is the boundary between mesosphere and thermosphere. these all boundaries are ranges between altitude of 0 to 80 km.

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.