Meiosis, which includes independent assortment of homologous chromosomes and chromosomal crossover, contributes to genetic diversity. Independent assortment of chromosomes is the random distribution of one chromosome per homologous chromosomal pair to each daughter cell during anaphase I. Chromosomal crossover, which begins in prophase I, results in genetic recombination between each tetrad (homologous chromosomes). Nondisjunction is not a correct option as this typically results in large scale genetic abnormalities and infertility which subsequently does not contribute to a population's long-term genetic diversity. 

Human female gametogenesis occurs through meiosis and results in three non-functional daughter cells known as polar bodies and one functional and much larger daughter cell called an ovum. Unequal division of cytoplasm during meiosis I and meiosis II towards only one of the daughter cells results in the ovum. Non-disjunction is the unequal assortment of chromosomes, not cytoplasm. Human female gametogenesis results in ovum while human male gametogenesis results in sperm. Mitosis does not result in gamete daughter cells but identical daughter cells as mitosis occurs in somatic (body or non-germ cells) cells. 

Germ cells give rise to gametes through meiosis. All of the other organisms listed are asexually reproducing organisms and therefore only undergo mitosis. 

Nondisjunction of homologous chromosomes may occur in anaphase I and nondisjunction of sister chromatids may occur in anaphase II. 

Independent assortment depends upon random alignment of homologous chromosomes in metaphase I which will result in randomly assorted chromosomes into two daughter cells at the end of meiosis I. Crossover, or recombination, occurs in prophase I which contributes to genetic diversity, but does not affect random alignment of homologous chromosomes. Spindles align chromosomes randomly in metaphase I, not anaphase I during which they are already "aligned" and are moving towards opposite poles of the cell.

In meiosis, the gametes are haploid having half the number of chromosomes of a diploid cell.  The gametes are the egg or sperm cells that combine in sexual reproduction.

Random rearranging of alleles on chromosomes that occurs as a result of homologous pairs lining up during metaphase is known as independent assortment and is a factor in genetic diversity. Cytokinesis is the physical process for cell division. Glycolysis is the process of breaking down sugars to generate ATP. G1 phase is the first of four phases of the cell cycle that takes place in eukaryotic cell division. Mitosis only has one metaphase, since the question stem indicates metaphase I, we know that the overall process is meiosis, during which there are two cell divisions.

Meiosis produces four genetically different haploid cells, which have half the chromosomes of diploid cells. Diploid cells are produced by mitosis. Transcription produces messenger RNA, and translation produces a chain of amino acids that is protein.

Only meiosis produces daughter cells that have half the number of copied chromosomes as the parent cells. This occurs in meiosis II and the importance of having daughter cells that are haploid is that fusion of those cells during sexual reproduction will create a cell with a normal amount of copied chromosomes (diploid), not more or less. Since mitosis deals with asexual reproduction there is no need to make haploid daughter cells.

Mitosis and meiosis, then, are two forms of cellular division and like all processes they can have problems.

DNA is both replicated (interphase) and pulled apart (anaphase) in both processes. Meiosis just goes through the cycle an additional time.

Finally, microtubules are the main component in the mitotic spindle for both meiosis and mitosis.

During anaphase I, it is just like mitosis. There is a pair of homologous chromosomes (two X's) and they separate into two daughter cells. Anaphase II is a continuation of cellular division so instead of separating a pair of homologous chromosomes it separates sister chromatids of one chromosome (one X) into two daughter cells.