Meiosis and Sexual Reproduction

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This set of flashcards covers vocabulary and key concepts related to meiosis, sexual reproduction, and genetic variation as discussed in the lecture notes.

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78 Terms

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Haploid

A cell that contains one complete set of chromosomes (n).

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Diploid

A cell that contains two complete sets of chromosomes (2n).

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Asexual reproduction

A mode of reproduction that does not involve the fusion of gametes and produces genetically identical offspring.

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Sexual reproduction

A process that involves the fusion of gametes, resulting in offspring with genetic variation.

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Gamete

A reproductive cell that is involved in sexual reproduction, containing half the number of chromosomes of a somatic cell.

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Mitosis

A type of cell division that produces two identical diploid daughter cells.

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Meiosis

A type of cell division that reduces the chromosome number by half, producing four haploid daughter cells.

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Crossing over

The exchange of genetic material between homologous chromosomes during meiosis, contributing to genetic diversity.

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Homologous chromosomes

Pairs of chromosomes that have the same length, shape, and carry genes for the same traits.

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Genetic diversity

Variability in the genetic makeup among individuals within a population.

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Cell division stages

The three stages of the sexual life cycle: mitosis, meiosis, and fertilization.

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Fertilization

The process where two gametes fuse to form a zygote.

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Sister chromatids

Identical copies of a chromosome connected by a centromere.

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Chromatid

A single thread of a duplicated chromosome.

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Karyotype

A photograph or diagram of the chromosomes in a cell used for analysis.

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Reduction division

The division that halves the number of chromosomes, characteristic of meiosis.

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Independent assortment

The random distribution of homologous chromosomes during meiosis.

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Nondisjunction

An error in meiosis when chromosomes fail to separate properly.

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Autosomal trisomy

A genetic condition where an individual has three copies of a chromosome instead of two.

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XXY Syndrome

Also known as Klinefelter's syndrome, a condition in males caused by an extra X chromosome.

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XO Syndrome

Also known as Turner syndrome, a condition in females caused by a missing X chromosome.

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Meiosis I

The first division of meiosis that separates homologous chromosomes.

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Meiosis II

The second division of meiosis that separates sister chromatids.

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Zygote

The fertilized egg that results from the fusion of gametes.

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Somatic cells

Non-reproductive cells that contain the diploid number of chromosomes.

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Centromere

The region of a chromosome where sister chromatids are joined.

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Bivalents

Paired homologous chromosomes that form during meiosis I.

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Tetrad

A group of four chromatids formed during meiosis by the pairing of two homologous chromosomes.

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Synapsis

The pairing of homologous chromosomes during meiosis.

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Metaphase I

The stage of meiosis I where homologous chromosomes align at the equatorial plane.

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Anaphase I

The stage of meiosis I where homologous chromosomes are pulled apart to opposite poles.

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Telophase I

The stage of meiosis I where the cell divides into two haploid cells.

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Prophase II

The stage of meiosis II where chromosomes condense and spindle fibers form.

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Metaphase II

The stage of meiosis II where chromosomes align at the equatorial plane.

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Anaphase II

The stage of meiosis II where sister chromatids separate.

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Telophase II

The final stage of meiosis II characterized by the formation of four haploid cells.

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Parental chromosomes

The original chromosomes contributed by the parents in sexual reproduction.

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Chromosome duplication

The process by which a cell creates an identical copy of its chromosomes.

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Genetic recombination

The process by which genetic material is mixed and shuffled during sexual reproduction.

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Clonal organisms

Organisms that reproduce asexually and are genetically identical to the parent.

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Novel genetic combinations

New genetic variations formed through sexual reproduction.

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Sister chromatid separation

The process that occurs during anaphase of meiosis II, where sister chromatids split apart.

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Haploid cells

Cells that contain half the number of chromosomes, represented as n.

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Diploid cells

Cells that contain two complete sets of chromosomes, represented as 2n.

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Gamete fusion

The process of two gametes coming together to form a zygote.

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Meiotic non-disjunction

Occurs when chromosomes fail to separate properly during meiosis.

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Fertilization variations

Different genetic combinations that arise from the fusion of gametes from two parents.

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Genetic variation mechanisms

Methods through which genetic diversity is generated, including crossing over, independent assortment, and random fertilization.

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Human somatic cells

Cells of the human body that are not involved in reproduction, having 46 chromosomes.

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Alleles

Different versions of the same gene that can produce varying traits.

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Parental generation

The original generation that contributes to the offspring in genetic studies.

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Offspring generation

The next generation produced from parental organisms.

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Meiosis significance

Crucial for producing genetic variation and maintaining chromosome numbers across generations.

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Sperm cell

The male gamete involved in sexual reproduction.

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Egg cell

The female gamete involved in sexual reproduction.

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Diploid number

The total number of chromosomes in diploid cells, e.g., 46 in humans.

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Fertilization process

The union of male and female gametes to form a zygote.

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Microtubule spindle apparatus

Structure that helps separate chromosomes during cell division.

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Chiasma

The point of crossing over between homologous chromosomes.

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Reproductive strategies

Different methods organisms use to reproduce, either sexually or asexually.

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Mitosis outcome

Results in two identical daughter cells with the same diploid number.

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Meiosis outcome

Results in four genetically diverse haploid cells.

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DNA replication

The process of duplicating the cell's DNA before division.

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Genetic disorder

A disease caused by an abnormality in an individual’s genetic makeup.

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Chromosomal abnormalities

Alterations in chromosome number or structure, leading to genetic disorders.

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Mutation's role in variation

Changes in DNA that can lead to variation in offspring, especially in asexual reproduction.

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Life cycle stages

The series of developmental stages that organisms go through, including growth, reproduction, and death.

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Homologs

Refers to the homologous chromosomes that pair during meiosis.

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Meiotic error consequences

Can lead to genetic disorders in offspring, such as Down syndrome.

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Ploidy levels

The number of sets of chromosomes in a cell; haploid (n), diploid (2n), etc.

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Unique gametes

Gametes that differ genetically due to meiosis, contributing to diversity.

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Meiosis and genetic diversity

Meiosis introduces genetic variation through independent assortment and crossing over.

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Species survival

A function of genetic diversity, ensuring adaptability to environmental changes.

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Environmental stability and asexuality

In stable environments, asexual reproduction may be advantageous due to consistency in successful traits.

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Genetic trait inheritance

The transmission of genetic characteristics from parent to offspring.

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Non-crossover chromatids

Sister chromatids that remain identical due to lack of crossover.

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Allelic combinations

The various ways alleles can combine during gamete formation.

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Gamete production site

Occurs in reproductive organs, such as ovaries and testes.