Bio Meiosis & Chromosomes Test Review PDF
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Uploaded by ReverentColumbus3914
Minooka Community High School
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This document is a test review focusing on meiosis and chromosomes. It includes matching questions, vocabulary definitions, and comparisons between mitosis and meiosis. The document contains diagrams, questions, and answers. It is useful for secondary school biology students.
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# Test Review: Meiosis and Chromosomes ## Matching Match the descriptions to the correct stages of meiosis: | Stage | Description | |---|---| | Interphase | e. DNA replicated during the Synthesis (S-Phase). Chromatin is visible | | Prophase I | h. Synapsis occurs and tetrads form. Crossing over o...
# Test Review: Meiosis and Chromosomes ## Matching Match the descriptions to the correct stages of meiosis: | Stage | Description | |---|---| | Interphase | e. DNA replicated during the Synthesis (S-Phase). Chromatin is visible | | Prophase I | h. Synapsis occurs and tetrads form. Crossing over occurs when chromosomes exchange genetic information (recombination) | | Metaphase I | b. Tetrads align in the middle (in pairs) | | Anaphase I | d. Tetrads split into chromosomes. In other words, the homologous pairs separate. | | Telophase/Cytokinesis I | a. Two haploid daughter cells are produced | | Prophase II | f. Chromosomes supercoil to become visible in the two daughter cells produced previously in Meiosis I. | | Metaphase II | i. Chromosomes line up in 2 different cells. | | Anaphase II | c. Chromosomes split into sister chromatids in 2 different cells. | | Telophase/Cytokinesis II | g. Two cells each containing 2 haploid nuclei are formed, and 4 haploid daughter cells produced | ## Vocabulary Match the term to the correct definition: | Term | Definition | |---|---| | Synapsis | i. The homologous chromosomes joining/pairing up (synapsis) and form a tetrad. The sharing of genetic material between two nonsister chromatids in a homologous pair | | Nondisjunction | d. The failure of chromosomes to NOT separate during Anaphase I or 2 | | Gene | b. a section of chromosome that codes for a specific trait | | Telomere | a. the protective caps on your chromosomes that act like the aglet (plastic tip) on a shoelace and prevent chromosomes from unraveling | | Crossing over | i. The homologous chromosomes joining/pairing up (synapsis) and form a tetrad. The sharing of genetic material between two nonsister chromatids in a homologous pair | | Autosomes | h. the first 22 pairs of chromosomes (or 44 chromosomes) in a karyotype. Not involved in the determination of biological sex | | Haploid | f. the presence of a single set of chromosomes in an organism's cells | | Diploid | g. the presence of two complete set of chromosomes in an organism's cells | | Karyotype | e. An individual's complete set of chromosomes, a picture or map of an organism's chromosomes | ## Identifying Phases of Meiosis 19. Identify the phase of Meiosis I/II based on the pictures. Record your answers below the picture. - [ ] Metaphase I - [ ] Metaphase II - [ ] Prophase I - [ ] Prophase II - [ ] Telophase I - [ ] Telophase II - [ ] Anaphase I - [ ] Anaphase II 20. In what phase of Meiosis I does crossing over take place? - Prophase I 21. Why is crossing over important for creating variation amongst a species? It creates new combinations of alleles in gametes, leading to offspring with unique genetic makeup. ## Comparing Mitosis and Meiosis 22. Compare and Contrast Mitosis and Meiosis. Place the description in the correct box: | Mitosis | Meiosis | Both | |---|---|---| | b. Produces two identical diploid daughter cells | a. Produces four unique haploid daughter cells | | | k. Body Cells | j. Gametes | | | n. DNA is replicated once | | d. Goes through one division | | | | h. Types of cell division | | | | | | | | | | | | | | | | | | | | | | | | | | | | | ## Labeling a Diagram 23. Label the diagram using the following terms: - a. Centromere - b. Homologous Pair - c. Recombinant Chromatid/Crossing over - d. Sister Chromatids ## Haploid vs. Diploid 24. Using the diagram below, describe which cell is diploid or haploid by completing the red boxes: ![haploid vs diploid diagram](image-missing) - Cell A is haploid. - Cell B is diploid. 25. Which Cell from the table above would represent sex cells (gametes)? - Cell A 26. Which Cell from the table above would represent body cells (somatic cells)? - Cell B ## Haploid and Diploid Numbers 27. Fill in the table below with the haploid or diploid number: | Animal | Haploid (1 set) | Diploid (2 sets) | |---|---|---| | Deer | 28 | 56 | | Cobra | 42 | 84 | | Pheasant | 39 | 78 | | Horse| 6 | 12 | | Crocodile | 30 | 60 | ## Identifying Gametes 28. Which gamete below should NOT result from the parent cell shown? Highlight or circle the correct box. ![parent cell and gametes](image-missing) - The correct answer is **C** - The gamete in **C** is missing a large and a medium chromosome from the parent cell. ## Types of Mutations 29. Explain your answer to the above question. C is missing 1 large & 1 medium Chromosome (1 from each pair) haploid 30. Identify the type of mutation based on the definition. | Definition | Mutation Type | |---|---| | arise from an event termed unequal crossing-over that occurs during meiosis between misaligned homologous chromosomes in which a segment of a chromosome is copied and added to the chromosome. | duplication | | can be caused by errors in chromosomal crossover during meiosis involving a loss of a segment of chromosome, which causes several serious genetic diseases. | deletion | | occurs when a chromosome breaks at two points and the segment is reinserted in the reversed orientation | inversion | | occurs when a part of one chromosome breaks off and sticks to another non homologous chromosome. These “mutations” are an important cause of many types of lymphomas and leukemias | translocation | ## Identifying Mutations in Diagrams 31. Identify the mutation type based on the pictures. - A. deletion - B. duplication - C. inversion - D. translocation ## Completing a Table 32. Complete the table with the following information: | Definition | Term | # of chromosomes (humans) | |---|---|---| | The absence of one member of a pair of chromosomes. | monosomy | 45 | | a chromosomal condition characterised by an additional chromosome | trisomy | 47 | ## Identifying Sex from Karyotypes 33. Look at the following karyotypes and identify whether the individual is biologically male or female. ![Karyotypes](image-missing) - The first karyotype is male (XY) - The second karyotype is female (XX) ## Identifying Genetic Disorders 34. For each karyotype, identify the genetic disorder and its corresponding description: | Karyotype | Genetic Disorder | Description (monosomy or trisomy) | |---|---|---| | [KARYOTYPE 1](image-missing) | Down Syndrome | trisomy 21, 47, XY, +21 | | [KARYOTYPE 2](image-missing) | Turner Syndrome | monosomy of the sex chromosomes, 45, X | | [KARYOTYPE 3](image-missing) | Klinefelter Syndrome | trisomy of the sex chromosomes, 47, XXY | ## Identifying Mutations in a Karyotype 35. Identify the mutation in the below karyotype for chromosome m12. [KARYOTYPE](image-missing) - **d. Translocation** The diagram indicates that a part of another chromosome has been translocated onto chromosome m12, as it has two different colors.