Campbell Essential Biology with Physiology (6th Edition)
6th Edition
ISBN: 9780134711751
Author: Eric J. Simon, Jean L. Dickey, Jane B. Reece
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 9, Problem 9SQ
Summary Introduction
To explain: The extension of the Mendel’s model that could produce the variation in height of children that have tall parents.
Introduction: The Mendel model states that genes are present in the parents for the expression of the tall genes. The genes are transferred to the next generation after the process of recombination. Therefore, the children of tall parents will have tall children.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Many traits that people think about as "running in families" or as being heritable in plants or animals are not inherited in the simple patterns that Mendel observed. What are some of the reasons that a trait could be strongly affected by genes but still not show the simple ratios that Mendel observed?
Mendel’s experiments used plants that had traits which follow simple laws of dominance, segregation, and independent assortment. We have since learned that not all traits follow these simple laws. Give at least three examples of non-Mendelian inheritance patterns and explain how each differs from Mendel’s laws of inheritance.
Which of the following statements describes Mendel's law of independent assortment?
The inheritance of one characteristic does not affect the inheritance of another characteristic.
The inheritance pattern of one offspring will not affect the characteristics in a sibling.
The inheritance of one characteristic will determine the inheritance of other characteristics.
Only one characteristic is inherited in each generation.
Submit
Request Answer
Part B
In dogs, coat color (B or b) and hearing (D or d) are both genetically determined. If a dog is genotype BBDd, what gametes
could it make?
Select all that apply.
bd
BB
Dd
Bd
BD
bD
Chapter 9 Solutions
Campbell Essential Biology with Physiology (6th Edition)
Ch. 9 - The genetic makeup of an organism is called its...Ch. 9 - Which of Mendels laws is represented by each...Ch. 9 - Prob. 3SQCh. 9 - Prob. 4SQCh. 9 - Prob. 5SQCh. 9 - Prob. 6SQCh. 9 - Prob. 7SQCh. 9 - Prob. 8SQCh. 9 - Prob. 9SQCh. 9 - Prob. 10SQ
Ch. 9 - Prob. 11SQCh. 9 - Prob. 12SQCh. 9 - Incomplete dominance is seen in the inheritance of...Ch. 9 - Why was Henry VIII wrong to blame his wives for...Ch. 9 - Prob. 15SQCh. 9 - Prob. 16SQCh. 9 - Prob. 17SQCh. 9 - Prob. 18IMTCh. 9 - Prob. 19IMTCh. 9 - Prob. 20IMTCh. 9 - Prob. 21PSCh. 9 - Prob. 22PSCh. 9 - Prob. 23BSCh. 9 - Gregor Mendel never saw a gene, yet he concluded...Ch. 9 - Prob. 25BS
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- Pedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. Would you want to know the results of the cancer, heart disease, and TSD tests if you were Sarah and Adam? Is it their responsibility as potential parents to gather this type of information before they decide to have a child?arrow_forwardPedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. If Sarah carries the mutant cancer allele and Adam carries the mutant heart disease allele, what is the chance that they would have a child who is free of both diseases? Are these good odds?arrow_forwardA woman with fair skin, blond hair, and blue eyes gives birth to fraternal twins; the father has dark brown skin, dark hair, and brown eyes. One twin has blond hair, brown eyes, and light skin, and the other has dark hair, brown eyes, and dark skin. What Mendelian law does this real-life case illustrate and explain what this means in terms of the inherited alleles for these genes?arrow_forward
- Mendel's second postulate states: When two different unit factors responsible for a characteristic are found in the same organism, one will dominate and determine the characteristic type. Explain this postulate using modern genetic terms. Be sure to include the following terms in your explanation: dominant, recessive, allele, phenotype, genotype.arrow_forwardTwo brown-eyed parents produce a blue-eyed child. Grandparents suspect infidelity on the part of the mother since neither parent had blue eyes. Explain the Mendelian relationships. What type of inheritance is represented here?arrow_forwardGregor Mendel’s basic principles of inheritance say that each trait is controlled by just one gene with just two alleles, and that each allele is clearly dominant or recessive to the other. However, we now know that many (if not most) traits are not actually inherited according to these rules. Name and describe two other (i.e., non-Mendelian) inheritance patterns, including how each one works, and a give specific example of an actual trait that follows each pattern.arrow_forward
- The gene for pea pod colour has two alleles. The dominant allele, G, is associated with the dominant trait of green pea pod colour. The recessive allele, g, is associated with the recessive trait of yellow peapod colour. What is the phenotypic ratio of the offspring in terms of pea pod colour? Which of Mendel’s laws is responsible for the ability of a Punnett square to predict the correct genotype and phenotype ratios of the offspring?arrow_forwardWhich of the following is a conclusion in Mendel' independent assortment law? options: Genes controlling different traits segregate independently of each. Gametes from each plant have two copies of the gene for each trait. An organism's homologous chromosomes segregate from each other during gamete formation. The two genes for a trait carried by an organism may be identical to one anotherarrow_forwardTwo healthy parents have a child who is later diagnosed with cystic fibrosis. What is the genetic term for this kind of disease? Using Mendel’s pattern, pick a letter for this gene and give the genotypes of the parents and the child. What are the odds that their next child will also have cystic fibrosis?arrow_forward
- What is the hypothesis that Mendel's laws are based on?arrow_forwardThis exercise is designed to give you some practice with Punnett squares and Mendel's principals of inheritance. Melanin is a chemical pigment produced in our body that contributes greatly to our skin, eye, and hair pigmentation -it also relates to color of fur, feathers, and such in animals. In general, the more melanin that is produced, the darker the color. A few genes contribute to the type and amount of melanin that is produced. Most people produce melanin in their skin, because it helps protect against the damages caused by the sun. This is why people tan. There is, however, a particular set of recessive alleles that cause a person to produce little or no melanin, and we refer to this as albinism. An animal or person who has little or no melanin is referred to as albino, and this can manifest in hair, skin, and eyes. For humans, this can be a rather dangerous condition as albinos are far more susceptible to sun damage, particularly cancer. In this exercise, the alleles are as…arrow_forwardMendel’s observation that two different traits could be inherited independently of each other can be explained by understanding that: During meiosis, the process of chromosome assortment into daughter cells is random Alleles of the genes reside on homologous chromosomes All of the listed choices are correct During meiosis, maternal and paternal members of homologous chromosomes are distributed separately into daughter cellsarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Human Heredity: Principles and Issues (MindTap Co...BiologyISBN:9781305251052Author:Michael CummingsPublisher:Cengage Learning
Human Heredity: Principles and Issues (MindTap Co...
Biology
ISBN:9781305251052
Author:Michael Cummings
Publisher:Cengage Learning
How to solve genetics probability problems; Author: Shomu's Biology;https://www.youtube.com/watch?v=R0yjfb1ooUs;License: Standard YouTube License, CC-BY
Beyond Mendelian Genetics: Complex Patterns of Inheritance; Author: Professor Dave Explains;https://www.youtube.com/watch?v=-EmvmBuK-B8;License: Standard YouTube License, CC-BY