Biol 102 Practice midterm

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20 Terms

1
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Which of the following statements is false? Crossovers happen:

  • during synapsis

  • between non-sister chromatids

  • between sister chromatids

  • before sister chromatids separate

  • during the first meiotic division

  • between sister chromatids

2
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Mendel’s laws state that

  • alleles segregate equally and pairs of alleles assort independently

  • alleles segregate independently and pairs of alleles assort equally

  • a monohybrid cross demonstrates a phenotypic 3:1 ratio

  • a dihybrid cross demonstrates a phenotypic 9:3:3:1 ratio

  • intrachromosomal recombination produces parental progeny at 50%

  • alleles segregate equally and pairs of alleles assort independently

3
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According to Mendel’s laws of equal segregation and independent assortment, what ratio of progeny do you expect from a dihybrid testcross involving two unliked loci controlling independent traits?

  • 9:3:3:1

  • 3:1

  • 1:1

  • 1:1:1:1

  • none of the above

  • 1:1:1:1

4
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A parent that undergoes self-fertilization is heterozygous for a gene (A/a). What percent of the progeny will be expected to be heterozygous (A/a) for this gene?

  • ¼

  • 1/3

  • ½

  • 2/3

  • 3/4

  • 1/2

5
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A gene can have more than two alleles (T/F)

  • True

6
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A cell with 16 chromosomes after the first meiotic division is

  • diploid and contains 32 sister chromatids

  • diploid and is found in an organism with 2n = 16

  • haploid and contains no sister chromatids

  • haploid and is found in an organism with 2n = 32

  • none of the above

  • haploid and is found in an organism with 2n = 32

7
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The final products of mitosis of a diploid cell are identical, diploid daughter cells. The final products of meiosis of a diploid cell are __ daughter cells

  • non-identical, haploid

  • identical, haploid

  • identical, diploid

  • non-identical, diploid

  • non-identical, haploid

8
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You cross an A/a; B'/b; C/c; D/d individual to an A/A; B/b; c/c; D/d individual. If the four loci are unlinked, what proportion of the progeny are expected to be either A/a; b/b; c/c; D/D or A/a; B/b; c/c; d/d?

  • 1/64

  • 3/64

  • 1/32

  • 1/256

  • 1/16

  • 3/64

9
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Are the following progeny numbers consistent with the results expected from selfing a plant presumed to be a dihybrid of two independently assorting genes, A/a; B/b? (A =round shape; a = wrinkled shape; B = yellow; b = green.) What is the chi-squared (X2) value and degrees of freedom?

Phenotype Number

Round, Yellow 315

Wrinkled, Yellow 101

Round, Green 108

Wrinkled, Green 32

  • X2 = 0.47, degrees of freedom = 3

  • X2 = 0.47, degrees of freedom = 2

  • X2 = 0.15, degrees of freedom = 3

  • X2 = 0.15, degrees of freedom = 2

  • X2 = 0.15, degrees of freedom = 1

  • X2 = 0.47, degrees of freedom = 3

<ul><li><p>X2 = 0.47, degrees of freedom = 3</p></li></ul><p></p>
10
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You obtain a chi-squared value of 4.7. The degrees of freedom are 2. Assuming a cutoff

of p=0.05 for statistical significance, how do you interpret this result?

  • p < 0.05; these data are not consistent with the NULL hypothesis

  • p > 0.05; there is no reason to reject the NULL hypothesis

  • p < 0.05; there is no reason to reject the NULL hypothesis

  • p > 0.05; these data are not consistent with the 1:2:1 hypothesis

  • None of the other choices

  • p > 0.05; there is no reason to reject the NULL hypothesis

11
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<p>What is the most likely pattern of inheritance of the rare trait in this pedigree?</p><ul><li><p>autosomal recessive</p></li><li><p>autosomal dominant</p></li><li><p>X-linked recessive</p></li><li><p>X-linked dominant</p></li><li><p>mitochondrial</p></li></ul><p></p>

What is the most likely pattern of inheritance of the rare trait in this pedigree?

  • autosomal recessive

  • autosomal dominant

  • X-linked recessive

  • X-linked dominant

  • mitochondrial

  • X-linked recessive

<ul><li><p>X-linked recessive</p></li></ul><p></p>
12
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<p>Among the following options, what is the best evidence that the trait in this pedigree is autosomal dominant and not X-linked dominant?</p><ul><li><p>I-1 and III-1 are affected</p></li><li><p>II-2 is affected</p></li><li><p>III-1 is affected</p></li><li><p> IV-1 is unaffected</p></li><li><p>IV-3 is unaffected</p></li></ul><p></p>

Among the following options, what is the best evidence that the trait in this pedigree is autosomal dominant and not X-linked dominant?

  • I-1 and III-1 are affected

  • II-2 is affected

  • III-1 is affected

  • IV-1 is unaffected

  • IV-3 is unaffected

  • IV-1 is unaffected

<ul><li><p>IV-1 is unaffected</p></li></ul><p></p>
13
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<p>If the trait shown in the pedigree at right is X-linked recessive, what is the probability that a child of II-2 and II-3 will be affected?</p><ul><li><p>0</p></li><li><p>1/8</p></li><li><p> 1/4</p></li><li><p> 1/64</p></li><li><p> 1/16</p></li></ul><p></p>

If the trait shown in the pedigree at right is X-linked recessive, what is the probability that a child of II-2 and II-3 will be affected?

  • 0

  • 1/8

  • 1/4

  • 1/64

  • 1/16

  • 1/8

<ul><li><p>1/8</p></li></ul><p></p>
14
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The trait shown in the pedigree below is autosomal recessive. What is the probability that a child of II-2 and II-3 will be affected?

  • 0

  • 1/9

  • 1/4

  • 1/16

  • 1/9

<ul><li><p>1/9</p></li></ul><p></p>
15
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<p> The grandmother of III-1 was affected with an X-linked recessive disorder. While serving in the Peace Corps after college, III-1 met and married the square of her dreams, III-2. What is the probability that III-1 is a carrier of the mutant allele?</p><ul><li><p>1/4</p></li><li><p>1/3</p></li><li><p>1/2</p></li><li><p> 2/3</p></li><li><p>3/4</p></li></ul><p></p>

The grandmother of III-1 was affected with an X-linked recessive disorder. While serving in the Peace Corps after college, III-1 met and married the square of her dreams, III-2. What is the probability that III-1 is a carrier of the mutant allele?

  • 1/4

  • 1/3

  • 1/2

  • 2/3

  • 3/4

  • 1/2

<ul><li><p>1/2</p></li></ul><p></p>
16
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A woman with Turner syndrome is found to be colorblind (an X-linked recessive phenotype). Both her mother and her father have normal vision. What is the woman’s genotype? X^A = normal vision, X^a = colorblind, 0 = no chromosome

  • X^A / X^A

  • X^a / X^a

  • X^A / 0

  • X^a / 0

  • X^A/X^a

  • X^a / 0

17
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From question 16, what are the woman’s parents’ genotypes?

  • Mother X^A / X^a; Father X^A / Y

  • Mother X^A / X^a; Father X^a / Y

  • Mother X^a / X^a; Father X^A / Y

  • Mother X^A / X^A; Father X^A / Y

  • None of the other choices

  • mother X^A/ X^a; father X^A/Y

18
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From question 16, nondisjunction occurred in the father. (T/F)

  • true

Explanation: The woman has only one X^a and it must be from the mother. So the null (empty) gamete was from father, which means the nondisjunction occurred in the father’s meiosis.

19
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Which of the following karyotypes does NOT represent a male? X and Y denote a single copy of the X chromosome and a single copy of the Y chromosome, respectively, while A denotes a chromosome set.

  • XY AA in humans

  • XY AA in drosophila

  • XXY AA in cats

  • XXY AA in drosophila

  • All of the options above represent males

  • XXY AA in drosophila

20
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Two inbred lines of beans are intercrossed. In the F1, the variance in bean weight is measured at 15 g^2. The F1 is selfed; in the F2, the variance in bean weight is 61 g^2. Estimate the broad heritability of bean weight in the F2 population of this experiment.

  • 0.25

  • 0.33

  • 0.50

  • 0.66

  • 0.75

  • 0.75

<ul><li><p>0.75</p></li></ul><p></p>