Sexual Reproduction and Meiosis

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These flashcards cover the key vocabulary and concepts for Chapter 9, including the mechanisms of meiosis, genetic variation, and chromosomal disorders resulting from nondisjunction.

Last updated 9:25 AM on 7/2/26
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26 Terms

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Ploidy

The number of complete sets of chromosomes in a cell; for example, animals are mostly diploid while asexually reproducing organisms are haploid.

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Diploid

Cells or organisms containing two homologous sets of chromosomes (2n2n), with one set inherited from each parent.

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Haploid

Cells or organisms containing only a single set of chromosomes (1n1n), typical of asexually reproducing organisms and gametes.

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Homologous chromosomes

Pairs of chromosomes that are the same size, have the same centromere position, and carry the same genes, though they may have different alleles.

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Alleles

Variations or different versions of a single gene.

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Somatic cells

All body cells except for gametes; these cells are diploid (2n2n) and divide via mitosis.

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Gametes

Sex cells (sperm and egg cells) that are haploid (1n1n) and genetically unique, produced through meiosis.

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Mitosis

Somatic cell division that produces two genetically identical daughter cells for the purpose of growth and repair.

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Meiosis

Sex cell division in germ cells where DNA replicates once but the nucleus divides twice, yielding four genetically unique haploid gametes.

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Fertilization

The process where a haploid sperm (1n1n) fuses with a haploid egg (1n1n) to form a diploid zygote (2n2n).

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Zygote

A single-cell fertilized egg that contains 4646 chromosomes in 2323 pairs in humans.

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Germ cells

Specialized cells that undergo meiosis to produce haploid gametes.

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Interphase

The phase of the cell cycle preceding division where the cell grows and copies its DNA; it includes G1G1, SS (DNA synthesis), and G2G2 stages.

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Crossing-over

Also known as recombination; a process during Prophase I where homologous chromosome pairs exchange genetic material, giving rise to greater allele variations.

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Recombinant chromatid

A chromatid produced by the process of crossing over that contains a new combination of maternal and paternal genetic information.

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Random assortment

Also known as independent assortment; the process during Metaphase I where homologous chromosome pairs align independently and randomly at the metaphase plate.

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Random fertilization

A source of genetic diversity where any sperm can fuse with any egg, resulting in approximately 2232^{23} combinations per gamete and about 11 in 7070 trillion total possible combinations.

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Monozygotic twins

Identical twins formed from a single zygote that splits into two embryos.

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Dizygotic twins

Fraternal twins formed when two separate eggs are fertilized by two different sperm, resulting in two distinct zygotes.

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Nondisjunction

An error in meiosis, most common in Meiosis I, where chromosomes fail to separate properly, leading to gametes with extra or missing chromosomes.

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Aneuploidy

A condition characterized by an atypical chromosome number, such as having one extra (n+1n+1) or one missing (n1n-1) chromosome.

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Monosomic

A type of aneuploidy where a cell is missing a chromosome, represented as (n1n-1).

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Trisomic

A type of aneuploidy where a cell has an extra chromosome, represented as (n+1n+1); examples include Trisomy 21 and Trisomy 18.

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Turner syndrome

A sex chromosome abnormality with the genotype XO, occurring in approximately 11 in 20002000 females, characterized by short stature and infertility.

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Klinefelter syndrome

A sex chromosome abnormality with the genotype XXY, occurring in approximately 11 in 750750 males, characterized by tall stature and breast development.

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Polyploidy

A condition where an organism has extra complete sets of chromosomes (e.g., 3n3n, 4n4n, 8n8n). While fatal in humans, it is common and often beneficial in plants like bananas and strawberries.