Where does the Calvin cycle occur? There is a scheme of the chloroplast structure. The outer layer of the chloroplast is labeled

A. The inner layer of the chloroplast membrane is labeled
B. A column of little cisterns is labeled
C. One of the cisterns is labeled
D. The space inside the chloroplast between its structures is labeled E.

A. The inner layer of the chloroplast membrane is labeled

Explanation:

Usually in plants, carbon dioxide enters the interior part of leaf through the pores also known as stomata and then diffuses into the stroma of the chloroplast.

Unlike the reactions to light, which take place in the thylakoid membrane, the reactions of the Calvin cycle take place in the stroma, also called the internal space of the chloroplasts, so it also takes place in the coroplast's storma.

The enzymes of Calvin Cycle responsible for cabon fixation( Ribulose Biphospahte Carbonxylase) Rubisco  is  located  in the STROMA, together with  sugar and inorganic acids. The stroma is the fluid  portion, of chloroplasts, located  in the inner membrane outside the thylakoid membrane  . Therefore option A -The inner layer of the chloroplast membrane is labeled.  is the correct answer.

It is a light independent reaction  which makes use of ATPs and  NADPH from the light dependent reaction to synthesize  Carbohydrate(glucose), amino acid and lipds.

Explanation:

on the planet jupiter, the acceleration due to gravity is approximately 26 m s2 , roughly 2.7 times the acceleration due

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.