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AP Biology Exam Review Put Your Knowledge to the Test

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Title: AP Biology Exam Review Put Your Knowledge to the Test


1
AP Biology Exam ReviewPut Your Knowledge to the
Test
Enter the Game
How to play
2
How This Works
  • Read the Question
  • Click on the button of the right answer
  • If you are wrong you go back to the start, if you
    answer correctly, you move on.
  • Click on the buttons only, not the page

Enter the Game
3
Genetics
6
1
2
3
4
5
10
11
7
12
8
9
13
14
15
16
17
18
23
22
21
20
19
24
4
Genetics Continued
29
28
27
26
25
35
30
32
31
33
34
5
1. What are Mendels Laws?
A
Law of Segregation
B
Law of Independent assortment
C
Both Law of Segregation and Law of Independent
Assortment
6
Nope! Try Again
BACK TO QUESTION
7
Right!!!!!!!!
  • Both the Law of Segregation and the Law of
    Independent Assortment are included in Mendels
    Law
  • The Law of Segregation states that each allele
    segregates separately. One of each homologous
    chromosomes goes to each new cell.
  • The Law of Independent Assortment states that in
    a dihybrid cross, each trait is independent of
    the other.

BACK TO GENETICS PAGE
8
2. What is a Locus?
A
The copied strand of the chromosome.
B
Exact location on a chromosome where a gene is
located.
C
The offspring generation
9
Wrong! Try Again
BACK TO QUESTION
10
Right!!!!!!!!
  • A locus is the exact location on a chromosome
    where a gene is located

BACK TO GENETICS PAGE
11
3. What is progeny?
A
The offspring generation
B
The parent generation
C
A sex influenced trait
12
SORRY, Try again!
BACK TO QUESTION
13
RIGHT!
  • Progeny is the offspring generation of a test
    cross

BACK TO GENETICS PAGE
14
4. What is a homologous pair?
A
Every cell contains two copies of each chromosome
B
  • The chromosome and its copy

C
The original pair of chromosomes
15
Wrong Answer!
BACK TO QUESTION
16
RIGHT
  • In a homologous pair, every cell contains two
    copies of each chromosome

BACK TO GENETICS PAGE
17
5. Define an x-inactivation
A
A genetic defect on the x chromosome
B
  • The x chromosome replicates uncontrollable

C
  • One of the x chromosomes does not uncoil into
    chromatin, it becomes a barr body instead.

18
TRY AGAIN
BACK TO QUESTION
19
CORRECT
  • X-inactivation is when one of the x chromosomes
    does not uncoil into chromatin and becomes a barr
    body instead

BACK TO GENETICS PAGE
20
6. What is a test cross?
A
  • A cross between any two pair of alleles to find
    the progeny

When you are trying to figure out what the make
up of the allele is, A_ (either A or a), and you
cross it with a pure recessive allele
B
C
  • A test between progeny to find the parent
    generation

21
Sorry, try again
BACK TO QUESTION
22
Yeah!!
  • A test cross is when you are trying to figure out
    what the make up of the allele is, A_ (either A
    or a), and you cross it with a pure recessive
    allele

BACK TO GENETICS PAGE
23
7. In the genus Homo sapien, who is the
heterogametic sex?
A
Female
B
Either sex could be the heterogametic sex
C
Male
24
WRONG!
BACK TO QUESTION
25
RIGHT
  • In the genus Homo sapien, the male is the
    heterogametic sex

BACK TO GENETICS PAGE
26
8. In the genus Homo sapien, who is the
homogametic sex?
A
Female
B
Male
C
Either sex could be the homogametic sex
27
NOPE, TRY AGAIN!
BACK TO QUESTION
28
ALRIGHT!
  • In the genus Homo sapien, the female is the
    homogametic sex

BACK TO GENETICS PAGE
29
9. What is the genotype of the blood type A?
A
AA and AB
B
AB and AO
C
AA and AO
30
Sorry, wrong answer
BACK TO QUESTION
31
RIGHT!!
  • The genotype of blood type A is AA or AO

BACK TO GENETICS PAGE
32
10. What is the genotype of the blood type B?
A
BB and BO
B
BB and AB
C
AB and BO
33
WRONG
BACK TO QUESTION
34
YEP!
  • The genotype for blood type B is BO or BB

BACK TO GENETICS PAGE
35
11. What is the genotype of the blood type AB?
A
  • AB and AO

B
AB
C
AA and AB
36
TRY AGAIN
BACK TO QUESTION
37
RIGHT
  • The genotype for blood type AB is AB

BACK TO GENETICS PAGE
38
12. What is the genotype of the blood type O?
A
OO and BO
B
OO
C
AO and OO
39
Try Again!
BACK TO QUESTION
40
CORRECT!!!!
  • The Genotype for blood type O is OO

BACK TO GENETICS PAGE
41
13. What is pleiotrophy?
A
  • An inactive gene

B
A single gene which has multiple effects
C
A recessive gene that shows in the phenotype
42
Wrong, try again
BACK TO QUESTION
43
RIGHT
  • Pleiotrophy is a single gene which has multiple
    effects
  • An example would be Siamese cats

BACK TO GENETICS PAGE
44
14. What is epistasis?
A
  • A gene that expressed in the genotype but not
    shown in the phenotype

B
  • A gene which effects multiple characteristics

C
  • Two recessive genes which cause dominance not to
    show

45
Go Back and Try Again!
BACK TO QUESTION
46
Youre Right!!!
  • An epistasis is two recessive genes that cause
    dominance not to show
  • An example would be snapdragons

BACK TO GENETICS PAGE
47
15. What is polygenic inheritance?
A
A single gene which has multiple effects
B
  • A gene which shows no characteristics

C
  • A dominant trait that is not expressed

48
Nope, try again
BACK TO QUESTION
49
RIGHT!!!
  • Polygenic Inheritance is a single gene which has
    multiple effects
  • An example would be in skin color and height

BACK TO GENETICS PAGE
50
16. An environmentally produced phenotype that
stimulates the effects of a particular gene is
called
A
Genetic Drift
B
Industrial Melanism
C
A Phenocopy
51
SORRY, GO BACK !!!
BACK TO QUESTION
52
Correct!!!!
  • An environmentally produced phenotype that
    stimulates the effects of a particular gene is
    called a phenotype
  • Examples are tranquilizer

BACK TO GENETICS PAGE
53
17. Which genetic defect is the inability to
break down phenylalanine?
A
Tay-Sachs Syndrome
B
  • Phenylketonuria

C
Huntington Disease
54
WRONG
BACK TO QUESTION
55
RIGHT
  • The genetic disease that effects the inability to
    break down phenylalanine is phenylketonuria.

BACK TO GENETICS PAGE
56
18. Which genetic defect is characterized by
lipids causing nervous system disorder?
A
Tay-Sachs Syndrome
B
Phenylketonuria
C
Huntington Disease
57
Go Back and Try Again!
BACK TO QUESTION
58
RIGHT
  • Tay-Sachs syndrome is characterized by lipids
    causing a nervous system disorder.

BACK TO GENETICS PAGE
59
19. Which genetic disease starts at middle age
with mild mental illness?
A
Tay-Sachs Syndrome
B
Cystic Fibrosis
C
Huntington disease
60
Nope, try again
BACK TO QUESTION
61
RIGHT
  • Huntington disease is a genetic disease which
    starts at middle age with mild mental illness.

BACK TO GENETICS PAGE
62
20. Which genetic defect has sickle shaped cells
and abnormal hemoglobin?
A
Down Syndrome
B
Cystic Fibrosis
C
Sickle cell anemia
63
Sorry, wrong answer
BACK TO QUESTION
64
Correct!!!!
  • Sickle cell anemia is characterized by sickle
    shaped cells and abnormal hemoglobin.

BACK TO GENETICS PAGE
65
21. Which genetic disease causes problems with
blood clotting?
A
Sickle Cell Anemia
B
Hemophilia
C
Cystic Fibrosis
66
NO WAY!!
BACK TO QUESTION
67
RIGHT
  • Hemophilia is a genetic disease which causes
    problems with blood clotting.

BACK TO GENETICS PAGE
68
22. What is the inability to distinguish red from
green?
A
Sickle Cell Anemia
B
Hemophilia
C
Red-green colorblindness
69
SORRY, TRY AGAIN
BACK TO QUESTION
70
CORRECT
  • Red-green colorblindness is a genetic disorder
    which is characterized by the inability to
    distinguish red from green.

BACK TO GENETICS PAGE
71
23. What genetic disease is known as trisomy21?
A
Downs Syndrome
B
Tay-Sachs Syndrome
C
Red-Green Colorblindness
72
TRY AGAIN
BACK TO QUESTION
73
GOOD JOB
  • The genetic disease also know as trisomy 21 is
    Downs Syndrome.

BACK TO GENETICS PAGE
74
24. Which genetic disease causes the
deteriorating of muscles?
A
Cystic Fibrosis
B
Duchenes Muscular Dystrophy
C
Downs Syndrome
75
NOPE
BACK TO QUESTION
76
RIGHT!!!
  • Duchenes Muscular Dystrophy is a genetic disease
    which causes the deteriorating of muscles.

BACK TO GENETICS PAGE
77
25. Which genetic disease is caused by an X, X,
and Y chromosome?
A
Klinefelton syndrome
B
Downs Syndrome
C
Criduchat
78
WRONG ANSWER
BACK TO QUESTION
79
CORRECT
  • The genetic disease caused by an XXY chromosome
    is Klinefelton syndrome

BACK TO GENETICS PAGE
80
26. Which genetic disease is characterized by a
cat-like cry?
A
Criduchat
B
Downs Syndrome
C
Hemophilia
81
TRY AGAIN
BACK TO QUESTION
82
ALRIGHT!
  • The genetic disease characterized by a cat-like
    cry is Criduchat.

BACK TO GENETICS PAGE
83
27. What is deletion?
A
Sections of the chromosome are inverted
B
Sections of the chromosome are duplicated
C
Sections of the chromosome are deleted
84
Try again
BACK TO QUESTION
85
RIGHT!!!!
  • Deletion happens when sections of the chromosomes
    are deleted.

BACK TO GENETICS PAGE
86
28. What is inversion?
A
Sections of the chromosome are switched
B
Sections of the chromosome are duplicated
C
Sections of the chromosome are deleted
87
Sorry, Wrong Answer
BACK TO QUESTION
88
Yep!
  • Inversion is when sections of the chromosome are
    switched.

BACK TO GENETICS PAGE
89
29. What is translocation?
A
A section of one chromosome switches with a
section of another chromosome
B
Sections of the chromosome are switched
C
A section of the chromosome is deleted
90
Try again
BACK TO QUESTION
91
Good answer
  • Translocation is when a section of one chromosome
    switches with another chromosome.

BACK TO GENETICS PAGE
92
30. What is duplication?
A
Sections of the chromosome are deleted
B
Sections of the chromosome are switched
C
Sections of a chromosome replicate more than once
93
Wrong Answer
BACK TO QUESTION
94
Alright!
  • Duplication is when sections of a chromosome are
    duplicated more than once.

BACK TO GENETICS PAGE
95
31. What is nondisjunction?
A
There is a duplication of the chromosome
B
The homologous chromosomes do not separate at
interphase
C
One X chromosome is duplicated in chromosome 23
96
SORRY, TRY AGAIN
BACK TO QUESTION
97
GOOD JOB
  • Nondisjunction is when the homologous chromosomes
    do not separate at interphase.

BACK TO GENETICS PAGE
98
32. What is expressivity?
A
The degree to which a particular gene is
expressed
B
There is a duplication of chromosome 21
C
Recessive genes are expressed instead of dominant
genes
99
Go back and try again
BACK TO QUESTION
100
RIGHT!!!
  • Expressivity is the degree to which a particular
    gene is expressed.
  • An example would be sickle cells

BACK TO GENETICS PAGE
101
33. What is polyploidy?
A
Chromosome 21 duplicates more than once
B
There are more than two complete sets of
chromosomes
C
The X chromosome is expressed twice along with a
Y chromosome
102
NOPE, GO BACK
BACK TO QUESTION
103
RIGHT!!!
  • Polyploidy is when there are more than two
    complete sets of chromosomes.

BACK TO GENETICS PAGE
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