"Trace the pathway of sperm" from where they are specifically made to where they leave the body.
a. seminiferous tubule - straight tubule - rete testis - efferent tubule - epididymis - ductus/vas deferens - ejaculatory duct - prostatic urethra - membranous urethra - spongy/penile urethra
b. seminiferous tubule - straight tubule - rete testis - efferent tubule - epididymis - ductus/vas deferens - ejactulatory duct - membranous urethra - prostatic urethra - spongy/penile urethra
c. straight tubule - seminiferous tubule - rete testis - efferent tubule - epididymis - ductus/vas deferens - prostatic urethra - membranous urethra - spongy/penile urethra
d. seminiferous tubule - efferent tubule - rete testis - straight tubule - epididymis - ductus/vas deferens - - ampulla of the vas deferens/ ductus deferens - prostatic urethra - membranous urethra - spongy/penile urethra"

oxygen +1 most likely

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.

unicellular organisms, like bacteria, are able to perform all life functions within one single cell. multicellular organisms need many different types of cells to carry out the same life processes. each of these special types of cells has a different structure that it perform a specific function.