Campbell Biology Custom Stony Brook 10 Th Edition
Campbell Biology Custom Stony Brook 10 Th Edition
10th Edition
ISBN: 9781269870818
Author: Reece Urry Cain Wasserman Minorsky Jackson
Publisher: PEARSON
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Chapter 24.2, Problem 4CC

MAKE CONNECTIONS Ø Review the process of meiosis in Figure 13.8. Describe how an error during meiosis could lead to polyploidy.

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10:10 E ← sisAndMeiosis.docx FREE EDIT PDF FREE CONVERT PDF TO WORD 2. Why are chromosomes important? 3. How are meiosis I and meiosis II different? 1. What is the state of DNA at the end of meiosis I? What about at the end of meiosis II? 4. Why do you use non-sister chromatids to demonstrate crossing over? 7. Identify two ways that meiosis contributes to genetic recombination. 10. P FREE PDF FILLER 5. What combination of alleles could result from a crossover between BD and bd chromosomes? 8. Why is it necessary to reduce the number of chromosomes in gametes? 6. How many nuclei are present at the end of meiosis II? How many chromosomes are in each? a. Sperm Cell b. Egg Cell AP_5 c. Daughter Cell from Mitosis ON 5G I 9. Blue whales have 44 chromosomes in every cell. Determine how many chromosomes you would expect to find in the following: d. Daughter Cell from Meiosis II COUS ra PAGE 10... FREE CONVERT JPG TO PDF X OeScience Labs, 2016
The diagram below shows a cell during Meiosis II: a) What phase of Meiosis II is the cell in? How do you know? b) Assuming all of the chromosomes present during Meiosis II are shown in the figure above, how many chromosomes (counting homologous pairs as two chromosomes) does a gamete from this organism have? c) Draw the same cell during the same phase of Meiosis I. Label the elements
Genetic problems: Use the diagram below to figure out how each monosomy or trisomy can a) Normal X chromosome segregation b) Nondisjunction in meiosis I c) Nondisjunction in meiosis II Diploid cell at start of meiosis First meiotic division Nondisjunction Second meiotic division Nondisjunction 00 00 develop. Benjamim XCuinmi х Х х х Xх хх о о XX O 2. A color-blind man married a normal woman. Their daughter, who was phenotypically normal, married a normal man and the couple produced three children, a normal boy, a color-blind boy, and a color-blind girl. Further examination indicates that this girl has two X chromosomes. Explain the origin of the color- blind girl.
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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY