Male ejaculate can contain any where from 40 million to 1 billion sperm, though the average ejaculate contains between 100 and 400 million. 

The primary energy source of spermatozoa is fructose, produced by the seminal vesicle along with multiple amino acids, vitamin C, enzimes, and flavin. 

Fully formed spermatozoa from the seminal vesicles are transported to the epididymis, where they are stored for 2-3 months. During ejaculation, stored sperm are moved from the lower epididymis via peristaltic action of the muscle layers of the vas deferens, mixed with various fluids to form semen.  

Seminal fluid is formed by several glands: the prostate contributes proteolytic enzymes, citric acid, acid phosphatase, zinc, fibrinolysin, and prostate specific antigen. The seminal vesicles contribute various flavins, fructose, and amino acids. The bulbourethral glands secrete a mucus that allows the semen to travel rapidly through the urethra, potentially aiding its route toward the cervix.  

The prostate, a fleshy endocrine gland inferior to the outlet of the male bladder, secretes a slightly alkaline milky fluid that makes up one third of the volume of semen. This alkalinity helps neutralize the acid environment of the vagina, increasing the likelihood of conception. Lubrication of the urethra is provided by the bulbourethral gland, while fructose is produced within the seminal vesicles. The prostate does not take part in sperm production. 

The urethra travels through the corpus spongiosum, one of three cavernous bodies in the human penis. The other two cavernous bodies are a set of sponge-like erectile tissues called the corpus cavernosum. The vas deferens and epididymis are both part of the storage and transportation of semen. The vas deferens joins with the urethra in the penis to facilitate ejaculation.

The pudendal nerve transmits sensation from the external genitalia, the skin around the anus, and the perineum. It also provides motor function to several important structures in the area, including musculature of the pelvic floor, the external urethral sphincter, and the external anal sphincter. The other nerves listed do not provide any sensory or motor innervation to the genitals. 

Sperm development begins with spermatogonia, undifferentiated male germ cell of the seminiferous tubules. During spermatogenesis, these cells first divide via mitosis to form two primary spermatocytes. Those cells then divide meiotically to form two secondary spermatocytes, which then undergo meiosis II to become spermatids. Spermatids then mature further to form spermatozoa via the process of spermiogenesis.  

The process by which spermatids mature into motile spermatozoa is called spermiogenesis. It is the final stage of spermatogenesis. During spermiogenesis, a polarity develops within the cell, which defines the cell as having a head end and a tail end. An acrosmal cap is formed over the head of the sperm, and a tail is formed via the elongation of a centriole within the cell. 

The cap that forms over the head and anterior tail of the spermatozoa is known as the acrosome. It is derived from the golgi apparatus, an organelle within the sperm cell. The acrosome prevents premature fertilization of the egg outside of the uterus. Within the uterus there are several proteolytic and glycosidic enzymes that begin to break down the acrosome, rendering it capable of fertilization. When the sperm meets the egg, the acrosome is then able to bind to the egg's zona pellucida, which triggers further breakdown of the acrosome (known as the acrosome reaction). This further breakdown releases enzymes held within the acrosome that allow the sperm to penetrate the zona pellucida, allowing conception to occur.