a) Name the structures that: i) Carry water and mineral salts to the leaf ii) Prevents too much water loss from the upper surface of the leaf iii) Opens to allow gases to pass into and out of the leaf iv) Is the site for most of the photosynthesis taking place v) Is the layer where light is able to pass through directly b) How does a leaf protect itself from unwanted intruders like bacteria from getting in and stopping important reactants from going out? PLEASE ANSWERR

a) i) Xylem

   ii) Upper epidermis  

   iii) Stoma

   iv) Chroloplast  

   v) Palisade cell layer

b) By a waxy layer on the cuticle of the leaf

Explanation:

The plant's leaves have a large surface area that is capable of absorbing sunlight. The plant's waxy layer in the surface of the leaf protects it from the loss of water, as well as of diseases caused by the entry of microorganisms. The palisade cell's surface is a single layer of cells underneath the upper epidermis that is adapted to absorb light energy.

The waxy layer is a primary physical barrier composed of insoluble polymers and lipids whose function is to protect the leaves against the entry of harmful organisms including virus, bacteria and fungus. Moreover, the plant's waxy cuticle is also a barrier that prevents the loss of water and solutes.

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.