Campbell Biology, Books a la Carte Plus Mastering Biology with eText -- Access Card Package (10th Edition)
10th Edition
ISBN: 9780133922851
Author: Jane B. Reece, Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Robert B. Jackson
Publisher: PEARSON
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Chapter 23.3, Problem 2CC
Distinguish genetic draft from gene flow in terms of (a) how they occur and (b) their irnplications for future
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What is meant by the term genetic variation? Give two examplesof genetic variation . What causesgenetic variation at the molecular level?
Distinguish genetic drift from gene flow in terms of(a) how they occur and (b) their implications for futuregenetic variation in a population.
1a) Define the term linkage disequilibrium.
(b) Explain why it makes sense that natural selection can maintain linkage disequilibrium between two loci that are not physically linked when there is epistasis for fitness.
(c) Explain the role of linkage disequilibrium in employing QTL mapping as a way to investigate the genetic architecture of adaptive traits.
Chapter 23 Solutions
Campbell Biology, Books a la Carte Plus Mastering Biology with eText -- Access Card Package (10th Edition)
Ch. 23.1 - Explain why genetic Variation within a population...Ch. 23.1 - Ot all the mutations that occur in a population,...Ch. 23.1 - MAKE CONNECTIONS If a population stopped...Ch. 23.2 - A population has 700 individuals, 85 of genotype...Ch. 23.2 - The frequency of allele a is 0.45 for a population...Ch. 23.2 - WHAT IF? A locus that affects susceptibility to a...Ch. 23.3 - In what sense is natural selection more...Ch. 23.3 - Distinguish genetic draft from gene flow in terms...Ch. 23.3 - WH AT IF? Suppose two plant populations exchange...Ch. 23.4 - What is the relative fitness of a sterile mule?...
Ch. 23.4 - Explain why natural selection is the only...Ch. 23.4 - Prob. 3CCCh. 23 - Typically. most of the nucleotide variabillity...Ch. 23 - Is it circular reasoning to calculate p ond q from...Ch. 23 - Would two small, geographically isolated...Ch. 23 - How might secondary sex characteristics in males...Ch. 23 - Natural selection changes allele frequencies...Ch. 23 - Prob. 2TYUCh. 23 - Prob. 3TYUCh. 23 - There are 25 individuals in population 1, all with...Ch. 23 - Prob. 5TYUCh. 23 - EVOLUTION CONNECTION Using at least two examples,...Ch. 23 - Prob. 7TYUCh. 23 - Prob. 8TYUCh. 23 - SYNTHESI2E YOUR KNOWLEDGE This kettle lake forracd...
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- The use of nucleotide sequence data to measure genetic variability is complicated by the fact that the genes of higher eukaryotes are complex in organization and contain 5′ and 3′ flanking regions as well as introns. Researchers have compared the nucleotide sequence of two cloned alleles of the g-globin gene from a single individual and found a variation of 1 percent. Those differences include 13 substitutions of one nucleotide for another and 3 short DNA segments that have been inserted in one allele or deleted in the other. None of the changes takes place in the gene’s exons (coding regions). Why do you think this is so, and should it change our concept of genetic variation?arrow_forwardThe original source of all genetic variation is what?arrow_forwardChoose one human multifactorial condition and describe it in detail. Include a description of the condition, possible genetic and environmental components that cause the condition as well as an explanation of why it is difficult to study multifactorial conditions. Include references. PDF https://www.genetics.edu.au/PDF/Environmental_and_genetic_interactions_fact_sheet-CGE.pdfarrow_forward
- ln a population of turtles, there are yellow-green shells and green shells. The yellow shells are caused by a homozygous recessive gene and the green shells are caused by the dominant gene. Given the following data:AA = 340Aa = 270aa = 120 a) Calculate p and q. b) Use a chi square test to determine if these alleles are in Hardy-Weinberg equilibrium. Submit your answer as a pdf or doc file. Show your workarrow_forwardSteven Frank and Laurence Hurst argued that a cytoplasmically inherited mutation in humans that has severe effects in males but no effect in females will not be eliminated from a population by natural selection because only females pass on mtDNA (S. A. Frank and L. D. Hurst. 1996. Nature 383:224). Using this argument, explain why males with Leber hereditary optic neuropathy are more severely affected than females.arrow_forwardThe agouti gene determines coat colour in mice. Heterozygous mice have yellow coats, while homozygous dominant mice have black coats. However, having two copies of the recessive alleles is lethal. In a population of 2 000 mice, 1 082 mice have black coats. a) Calculate the frequency of each allele. Show all your work and express your answer as a value between 0 and 1 rounded to two decimal places. b) What percentage of the mouse population is expected to be carriers of the lethal allele? Show all your work and express your answer rounded to one decimal place. c) How many mice will die during fetal development? Show all your work and round your answer to the closest whole number.arrow_forward
- Asthma is a common medical condition that is influenced by genetics and environment. In the US, appraximately 9% of adults have asthma. A recent genome wide association study (GWAS) identifieda genetic variation that increases asthma risk by S0% when a single copy of the risk variant is present in a genome. Which value below would represent the approximate asthma risk of an individual with this genetic variation in their genome? Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a 59% b 50% 14.5% 9.5% e 9%arrow_forwardABO blood groups in humans are an example of discontinuous variation, whereas height is a example of continuous variation. Describe how these two examples differ in terms of genetic controlarrow_forwardWhat evolutionary factors can cause allele frequencies to change and possibly lead to a genetic polymorphism? Discuss the relative importance of each type of process.arrow_forward
- a.) If all the blue dots represent FST values between one species in the Americas and one species in Oceania, does this pattern of genetic similarity on the graph suggest that Native Americans and the people of Oceania followed very different migration routes? Why or why not? b.) Given the maximum possible FST value (based on how this statistic is calculated), is it feasible that all human populations have most of the genetic variation within a given population with very little genetic differentiation between any two populations? Give a reason for your answer. c.) Does the graph above suggest that interbreeding during these human contacts had a considerable effect on the gene pools of the two communities? Or is it more likely that only very limited or no interbreeding took place between islanders of Oceania and Native Americans from S. America? Give a reason for your answer.arrow_forwardScientific studies have shown that the majority of human genetic differences worldwide exist within groups (or races) rather than between groups. True or false?arrow_forwardDiscuss the role of mutation in the origin of genetic polymorphisms. Suppose that a genetic polymorphism involves two alleles at frequencies of 0.45 and 0.55. Describe three different scenarios to explain these observed allele frequencies. You can propose that the mutations that produced the polymorphism are neutral, beneficial, or deleterious.arrow_forward
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