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Testbank for Biology 2nd Edition from OpenStax College ISBN 9781947172517

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Testbank for Biology 2nd Edition from OpenStax College ISBN 9781947172517Chapter 1 1 Figure 1.6 1: C; 2: F; 3: A; 4: B; 5: D; 6: E. The original hypothesis is incorrect, as the coffeemaker works when plugged into the outlet. Alternative hypotheses include that the toaster might be broken or that the toaster wasn't turned on. 3 Figure 1.16 Communities exist within populations which exist within ecosystems. 4 B 6 D 8 C 10 C 12 B 14 D 16 Answers will vary, but should apply the steps of the scientific method. One possibility could be a car which doesn’t start. The hypothesis could be that the car doesn’t start because the battery is dead. The experiment would be to change the battery or to charge the battery and then check whether the car starts or not. If it starts, the problem was due to the battery, and the hypothesis is accepted. 18 Answers will vary. Topics that fall inside the area of biological study include how diseases affect human bodies, how pollution impacts a species’ habitat, and how plants respond to their environments. Topics that fall outside of biology (the “study of life”) include how metamorphic rock is formed and how planetary orbits function. 20 Answers will vary. Layers of sedimentary rock have order but are not alive. Technology is capable of regulation but is not, of itself, alive. 22 During your walk, you may begin to perspire, which cools your body and helps your body to maintain a constant internal temperature. You might also become thirsty and pause long enough for a cool drink, which will help to restore the water lost during perspiration. Chapter 2 1 Figure 2.3 Carbon-12 has six neutrons. Carbon-13 has seven neutrons. 2 | P a g e3. Figure 2.24 C 3 A 6 C 8 D 10C 12 D 14 Ionic bonds are created between ions. The electrons are not shared between the atoms, but rather are associated more with one ion than the other. Ionic bonds are strong bonds, but are weaker than covalent bonds, meaning it takes less energy to break an ionic bond compared with a covalent one. 16 Buffers absorb the free hydrogen ions and hydroxide ions that result from chemical reactions. Because they can bond these ions, they prevent increases or decreases in pH. An example of a buffer system is the bicarbonate system in the human body. This system is able to absorb hydrogen and hydroxide ions to prevent changes in pH and keep cells functioning properly. 18 Carbon is unique and found in all living things because it can form up to four covalent bonds between atoms or molecules. These can be nonpolar or polar covalent bonds, and they allow for the formation of long chains ofcarbon molecules that combine to form proteins and DNA. Chapter 3 1 Figure 3.5 Glucose and galactose are aldoses. Fructose is a ketose. 3 Figure 3.33 Adenine is larger than cytosine and will not be able to base pair properly with the guanine on the opposing strand. This will cause the DNA to bulge. DNA repair enzymes may recognize the bulge and replace the incorrect nucleotide. 4 C 6 A 8 D 10 B 12 D 14 C 3 | P a g e16 B 18 C 20 C 21 Biological macromolecules are organic because they contain carbon. 23 Amino acids can be linked into long chains through condensation reactions. One of the hydrogen atoms bonded to the nitrogen atom of an amino acid reacts with the –OH group attached to the terminal carbon on another amino acid. Since both ends of the molecule can participate in condensation reactions, peptide bonds can be made in both directions to create a long amino acid chain. 25 The β 1-4 glycosidic linkage in cellulose cannot be broken down by human digestive enzymes. Herbivores such as cows, koalas, and buffalos are able to digest grass that is rich in cellulose and use it as a food source because bacteria and protists in their digestive systems, especially in the rumen, secrete the enzyme cellulase. Cellulases can break down cellulose into glucose monomers that can be used as an energy source by the animal. 27 Fat serves as a valuable way for animals to store energy. It can also provide insulation. Waxes can protect plant leaves and mammalian fur from getting wet. Phospholipids and steroids are important components of animal cell membranes, as well as plant, fungal, and bacterial membranes. 29 Fats have a higher energy density than carbohydrates (averaging 9kcal/gram versus 4.3kcal/gram respectively). Thus, on a per gram basis, more energy can be stored in fats than can be stored in carbohydrates. Additionally, fats are packaged into spherical globules to minimize interactions with the water-based plasma membrane, while glycogen is a large branched carbohydrate that cannot be compacted for storage. 31 A change in gene sequence can lead to a different amino acid being added to a polypeptide chain instead of the normal one. This causes a change in protein structure and function. For example, in sickle cell anemia, the hemoglobin β chain has a single amino acid substitution—the amino acid glutamic acid in position six is substituted by valine. Because of this change, hemoglobin molecules form aggregates, and the disc- shaped red blood cells assume a crescent shape, which results in serious health problems. 33 The protein must form a channel in the plasma membrane that allows water into the cell since water cannot cross the plasma membrane by itself. Since aquaporins are embedded in the plasma membrane and connect with both the intracellular and extracellular spaces, it must be amphipathic like the plasma membrane. The top and bottom of the protein must contain charged or polar amino acids (hydrophilic) to interact with the aqueous environments. The exterior transmembrane region must contain non- polar amino acids (hydrophobic) that can interact with the phospholipid tail. However, the inside of this channel must contain hydrophilic amino acids since they will interact with the traveling water molecules. 4 | P a g e35 The four types of RNA are messenger RNA, ribosomal RNA, transfer RNA, and microRNA. Messenger RNA carries the information from the DNA that controls all cellular activities. The mRNA binds to the ribosomes that are constructed of proteins and rRNA, and tRNA transfers the correct amino acid to the site of protein synthesis. microRNA regulates the availability of mRNA for translation. Chapter 4 1 Figure 4.7 Substances can diffuse more quickly through small cells. Small cells have no need for organelles and therefore do not need to expend energy getting substances across organelle membranes. Large cells have organelles that can separate cellular processes, enabling them to build molecules that are more complex. 3 Figure 4.18 It would end up on the outside. After the vesicle passes through the Golgi apparatus and fuses with the plasma membrane, it turns inside out. 4 C 6 D 8 D 10 B 12 D 14 A 16 C 18 D 20 D 22 C 24 D 25 A light microscope would be ideal when viewing a small living organism, especially when the cell has been stained to reveal details. 27 A transmission electron microscope would be ideal for viewing the cell’s internal structures, because many of the internal structures have membranes that are not visible by the light microscope. 29 The cell theory states: All living things are made of cells.;Cells are the most basic unit of life.;New cells arise from existing cells. All humans are multicellular organisms whose smallest building blocks are cells. Adult humans begin with the fusion of a male gamete cell with a female gamete cell to form a fertilized egg (single cell). That cell then divides into two cells, which each divides into two more cells, and so forth until all the cells of a human embryo are made. As the embryo passes through all the 5 | P a g edevelopmental stages to make an adult human, the cells that are added arise from division of existing cells. 31 Some microbes are beneficial. For instance, E. coli bacteria populate the human gut and help break down fiber in the diet. Some foods such as yogurt are formed by bacteria. 33 Both are similar in that they are enveloped in a double membrane, both have an intermembrane space, and both make ATP. Both mitochondria and chloroplasts have DNA, and mitochondria have inner folds called cristae and a matrix, while chloroplasts have chlorophyll and accessorypigments in the thylakoids that form stacks (grana) and a stroma. 35 “Form follows function” refers to the idea that the function of a body part dictates the form of that body part. As an example, compare your arm to a bat’s wing. While the bones of the two correspond, the parts serve different functions in each organism and their forms have adapted to follow that function. 37 Centrioles and flagella are alike in that they are made up of microtubules. In centrioles, two rings of nine microtubule “triplets” are arranged at right angles to one another. This arrangement does not occur in flagella. 39 A macrophage engulfs a pathogen by rearranging its actin microfilaments to bend the plasma membrane around the pathogen. Once the pathogen is sealed in an endosome inside the macrophage, the vesicle is walked along microtubules until it combines with a lysosome to digest the pathogen. 41 They differ because plant cell walls are rigid. Plasmodesmata, which a plant cell needs for transportation and communication, are able to allow movement of really large molecules. Gap junctions are necessary in animal cells for transportation and communication. 43 E. coli infections generally cause food poisoning, meaning that the invading bacteria cross from the lumen of the gut into the rest of the body. Tight junctions hold the epithelial layer that lines the digestive tract together so that the material that crosses into the body is tightly regulated. One way E. coli can avoid this regulation is to destroy the tight junctions so that it can enter the body between the epithelial cells, rather than having to go through the cells. Chapter 5 1 Figure 5.12 No, it must have been hypotonic as a hypotonic solution would cause water to enter the cells, thereby making them burst. 3 Figure 5.19 A decrease in pH means an increase in positively charged H+ ions, and an increase in the electrical gradient across the membrane. The transport of amino acids into the cell will increase. 6 | P a g e4 A 6 A 8 C 10 A 12 D 14 D 16 B 18 C 20 B 21 The fluid characteristic of the cell membrane allows greater flexibility to the cell than it would if the membrane were rigid. It also allows the motion of membrane components, required for some types of membrane transport. 23 Peripheral proteins can bind to other molecules in the extracellular space. However, they cannot directly transmit a signal to the inside of the cell since they do not have a transmembrane domain (region that goes through the plasma membrane to the inside of the cell). They must associate with integral membrane proteins in order to pass the signal to the inside of the cell. 25 Water moves through a membrane in osmosis because there is a concentration gradient across the membrane of solute and solvent. The solute cannot effectively move to balance the concentration on both sides of the membrane, so water moves to achieve this balance. 27 Decreasing temperature will decrease the kinetic energy in the system. A lower temperature means less energy in the molecules, so they will move at a slower speed. Lowering temperature also decreases the kinetic energy of the molecules in the plasma membrane, compressing them together. This increases the density of the plasma membrane, which slows diffusion into the cell. 29 The cell harvests energy from ATP produced by its own metabolism to power active transport processes, such as the activity of pumps. 31 Intestinal epithelial cells use active transport to fulfill their specific role as the cells that transfer glucose from the digested food to the bloodstream. Intestinal cells are exposed to an environment with fluctuating glucose levels. Immediately after eating, glucose in the gut lumen will be high, and could accumulate in intestinal cells by diffusion. However, when the gut lumen is empty, glucose levels are higher in the intestinal cells. If glucose moved by facilitated diffusion, this would cause glucose to flow back out of the intestinal cells and into the gut. Active transport proteins ensure that glucose moves into the intestinal 7 | P a g ecells, and cannot move back into the gut. It also ensures that glucose transport continues to occur even if high levels of glucose are already present in the intestinal cells. This maximizes the amount of energy the body can harvest from food. 33 The proteins allow a cell to select what compound will be transported, meeting the needs of the cell and not bringing in anything else. Chapter 6 1 Figure 6.8 A compost pile decomposing is an exergonic process; enthalpy increases (energy is released) and entropy increases (large molecules are broken down into smaller ones). A baby developing from a fertilized egg is an endergonic process; enthalpy decreases (energy is absorbed) and entropy decreases. Sand art being destroyed is an exergonic process; there is no change in enthalpy, but entropy increases. A ball rolling downhill is an exergonic process; enthalpy decreases (energy is released), but there is no change in entropy. 3 Figure 6.14 Three sodium ions could be moved by the hydrolysis of one ATP molecule. The ∆G of the coupled reaction must be negative. Movement of three sodium ions across the membrane will take 6.3 kcal of energy (2.1 kcal × 3 Na+ ions = 6.3 kcal). Hydrolysis of ATP provides 7.3 kcal of energy, more than enough to power this reaction. Movement of four sodium ions across the membrane, however, would require 8.4 kcal of energy, more than one ATP molecule can provide. 4 C 6 C 8 B 10A 12 A 14 C 16 Physical exercise involves both anabolic and catabolic processes. Body cells break down sugars to provide ATP to do the work necessary for exercise, such as muscle contractions. This is catabolism. Muscle cells also must repair muscle tissue damaged by exercise by building new muscle. This is anabolism. 18 A spontaneous reaction is one that has a negative ∆G and thus releases energy. However, a spontaneous reaction need not occur quickly or suddenly like an instantaneous reaction. It may occur over long periods due to a large energy of activation, which prevents the reaction from occurring quickly. 20 The ant farm had lower entropy before the earthquake because it was a highly ordered system. After the earthquake, the system became much more disordered and 8 | P a g ehad higher entropy. 22 The activation energy for hydrolysis is very low. Not only is ATP hydrolysis an exergonic process with a large −∆G, but ATP is also a very unstable molecule that rapidly breaks down into ADP + Pi if not utilized quickly. Thissuggests a very low EA since it hydrolyzes so quickly. 24 Feedback inhibition allows cells to control the amounts of metabolic products produced. If there is too much of a particular product relative to the cell’s needs, feedback inhibition effectively causes the cell to decrease production of that particular product. In general, this reduces the production of superfluous products and conserves energy, maximizing energy efficiency. Chapter 7 1 Figure 7.11 After DNP poisoning, the electron transport chain can no longer form a proton gradient, and ATP synthase can no longer make ATP. DNP is an effective diet drug because it uncouples ATP synthesis; in other words, after taking it, a person obtains less energy out of the food he or she eats. Interestingly, one of the worst side effects of this drug is hyperthermia, or overheating of the body. Since ATP cannot be formed, the energy from electron transport is lost as heat. 3 Figure 7.14 The illness is caused by lactate accumulation. Lactate levels rise after exercise, making the symptoms worse. Milk sickness is rare today but was common in the midwestern United States in the early1800s. 4 A 6 C 8 B 10 C 12 C 14 A 16 A 18 ATP provides the cell with a way to handle energy in an efficient manner. The molecule can be charged, stored, and used as needed. Moreover, the energy from hydrolyzing ATP is delivered as a consistent amount. Harvesting energy from the bonds of several different compounds would result in energy deliveries of different quantities. 20 All cells must consume energy to carry out basic functions, such as pumping ions across membranes. A red blood cell would lose its membrane potential if glycolysis were blocked, and it would eventually die. 22 Q and cytochrome c are transport molecules. Their function does not result directly in 9 | P a g eATP synthesis in that they are not pumps. Moreover, Q is the only component of the electron transport chain that is not a protein. Ubiquinone and cytochrome c are small, mobile electron carriers, whereas the other components of the electron transport chain are large complexes anchored in the inner mitochondrial membrane. 24 Fermentation uses glycolysis only. Anaerobic respiration uses all three parts of cellular respiration, including the parts in the mitochondria like the citric acid cycle and electron transport; it also uses a different final electron acceptor instead of oxygen gas. 26 Citrate can inhibit phosphofructokinase by feedback regulation. Chapter 8 1 Figure 8.6 Levels of carbon dioxide (a necessary photosynthetic substrate) will immediately fall. As a result, the rate of photosynthesis will be inhibited. 3. Figure 8.18 D 3 A 6 B 8 B 10 A 12 C 14 A 16 D 18 C 20 C 21 The outcome of light reactions in photosynthesis is the conversion of solar energy into chemical energy that the chloroplasts can use to do work (mostly anabolic production of carbohydrates from carbon dioxide). 23 The energy carriers that move from the light-dependent reaction to the light- independent one are “full” because they bring energy. After the energy is released, the “empty” energy carriers return to the light-dependent reaction to obtain more energy. There is not much actual movement involved. Both ATP and NADPH are produced in the stroma where they are also used and reconverted into ADP, Pi, and NADP+. 25 The stomata regulate the exchange of gases and water vapor between a leaf and its surrounding environment. When the stomata are closed, the water molecules cannot escape the leaf, but the leaf also cannot acquire new carbon dioxide molecules from the environment. This limits the light-independent reactions to only continuing until the 10 | P a g ecarbon dioxide stores in the leaf are depleted. 27 Both of these molecules carry energy; in the case of NADPH, it has reducing power that is used to fuel the process of making carbohydrate molecules in light-independent reactions. 29 Because RuBP, the molecule needed at the start of the cycle, is regenerated from G3P. 31 Because G3P has three carbon atoms, and each turn of the cycle takes in one carbon atom in the form of carbon dioxide. 33 In the defined ecosystem, energy would radiate from the Sun, and be absorbed by the chlorophyll in the leaves of the tree. Photosynthesis would occur in the leaves, transforming the light energy into stored chemical energy in the covalent bonds of carbon molecules. The giraffe would eat the leaves of the tree, and digest the carbon molecules to release energy. In the same ecosystem, nutrients would cycle between the tree and the giraffe. The giraffe would consume oxygen and release carbon dioxide as its cells perform aerobic respiration to create chemical energy. The tree will consume the released carbon dioxide during photosynthesis to create its own stored chemical energy, and release oxygen as a by- product. Chapter 9 1 Figure 9.8 C. The downstream cellular response would be inhibited. 3 Figure 9.17 C. 5 B 7 B 9 C 11 C 13 B 15 B 17 C 19 D 21 D 23 Intracellular signaling occurs within a cell, and intercellular signaling occurs between cells. 25 Internal receptors are located inside the cell, and their ligands enter the cell to bind 11 | P a g ethe receptor. The complex formed by the internal receptor and the ligand then enters the nucleus and directly affects protein production by binding to the chromosomal DNA and initiating the making of mRNA that codes for proteins. Cell-surface receptors, however, are embedded in the plasma membrane, and their ligands do not enter the cell. Binding of the ligand to the cell-surface receptor initiates a cell signaling cascade and does not directly influence the making of proteins; however, it may involve the activation of intracellular proteins. 27 Insulin’s receptor is an enzyme-linked transmembrane receptor, as can be determined from the “tyrosine kinase” in its name. This receptor is embedded in the plasma membrane, and insulin binds to its extracellular (outer) surface to initiate intracellular signaling cascades. Normally, steroid hormones cross the plasma membrane to bind with intracellular receptors. These intracellular hormone-receptor complexes theninteract directly with DNA to regulate transcription. This limits steroid hormones to be small, non-polar molecules so they can cross the plasma membrane. However, since insulin does not have to cross into the cell it could be large or polar (it is a small, polar molecule). 29 The binding of the ligand to the extracellular domain would activate the pathway normally activated by the receptor donating the intracellular domain. 31 If a kinase is mutated so that it is always activated, it will continuously signal through the pathway and lead to uncontrolled growth and possibly cancer. If a kinase is mutated so that it cannot function, the cell will not respond to ligand binding. 33 Possible explanations: EGFR dimer cannot separate.An upstream mutation (in Ras, Raf, MEK) constitutively activates the signaling cascade.ERK has a mutation that prevents it from binding to its phosphatase.The cell has a mutation preventing the expression or function of the ERK-specific phosphatase. 35 Multicellular organisms must coordinate many different events in different cell types that may be very distant from each other. Single-celled organisms are only concerned with their immediate environment and the presence of other cells in the area. Chapter 10 1 Figure 10.6 D. The kinetochore becomes attached to the mitotic spindle. Sister chromatids line up at the metaphase plate. Cohesin proteins break down and the sister chromatids separate. The nucleus reforms and the cell divides. 3 Figure 10.14 D. E6 binding marks p53 for degradation. 4 C 6 D 8 B 10 B 12 | P a g e12 D 14 A 16 A 18 D 20 C 22 C 24 D 26 C 28 Human somatic cells have 46 chromosomes: 22 pairs and 2 sex chromosomes that may or may not form a pair. This is the 2n or diploid condition. Human gametes have 23 chromosomes, one each of 23 unique chromosomes, one of which is a sex chromosome. This is the n or haploid condition. 30 The DNA double helix is wrapped around histone proteins to form structures called nucleosomes. Nucleosomes and the linker DNA in between them are coiled into a 30- nm fiber. During cell division, chromatin is further condensed by packing proteins. 32 The mitotic spindle is formed of microtubules. Microtubules are polymers of the protein tubulin; therefore, it is the mitotic spindle that is disrupted by these drugs. Without a functional mitotic spindle, the chromosomes will not be sorted or separated during mitosis. The cell will arrest in mitosis and die. 34 Many cells temporarily enter G0 until they reach maturity. Some cells are only triggered to enter G1 when the organism needs to increase that particular cell type. Some cells only reproduce following an injury to the tissue. Some cells never divide once they reach maturity. 36 The G1 checkpoint monitors adequate cell growth, the state of the genomic DNA, adequate stores of energy, and materials for S phase. At the G2 checkpoint, DNA is checked to ensure that all chromosomes were duplicated and that there are no mistakes in newly synthesized DNA. Additionally, cell size and energy reserves are evaluated. The M checkpoint confirms the correct attachment of the mitotic spindle fibers to the kinetochores. 38 Cdk must bind to a cyclin, and it must be phosphorylated in the correct position to become fully active. 40 If one of the genes that produces regulator proteins becomes mutated, it produces a malformed, possibly non-functional, cell-cycle regulator, increasing the chance that 13 | P a g emore mutations will be left unrepaired in the cell. Each subsequent generation of cells sustains more damage. The cell cycle can speed up as a result of the loss of functional checkpoint proteins. The cells can lose the ability to self-destruct and eventually become “immortalized.” 42 Regulatory mechanisms that might be lost include monitoring of the quality of the genomic DNA, recruiting of repair enzymes, and the triggering of apoptosis. 44 The common components of eukaryotic cell division and binary fission are DNA duplication, segregation of duplicated chromosomes, and division of the cytoplasmic contents. Chapter 11 1 Figure 11.9 Yes, it will be able to reproduce asexually. 2 C 4 D 6 A 8 C 10 B 12 D 14 D 16 A 18 C 19 During the meiotic interphase, each chromosome is duplicated. The sister chromatids that are formed during synthesis are held together at the centromere region by cohesin proteins. All chromosomes are attached to the nuclear envelope by their tips. As the cell enters prophase I, the nuclear envelope begins to fragment and the proteins holding homologous chromosomes locate each other. The four sister chromatids align lengthwise, and a protein lattice called the synaptonemal complex is formed between them to bind them together. The synaptonemal complex facilitates crossover between nonsister chromatids, which is observed as chiasmata along the length of the chromosome. As prophase I progresses, the synaptonemal complex breaks down and the sister chromatids become free, except where they are attached by chiasmata. At this stage, the four chromatids are visible in each homologous pairing and are called a tetrad. 21 In metaphase I, the homologous chromosomes line up at the metaphase plate. In anaphase I, the homologous chromosomes are pulled apart and move to opposite poles. Sister chromatids are not separated until meiosis II. The fused kinetochore formed during meiosis I ensures that each spindle microtubule that binds to the tetrad will attach 14 | P a g e

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Student Solution Manual OpenStax Biology 2nd Edition
Table of Contents
Chapter 1 ................................................................................................................................. 2
Chapter 2 ................................................................................................................................. 2
Chapter 4 ................................................................................................................................. 5
Chapter 5 ................................................................................................................................. 6
Chapter 6 ................................................................................................................................. 8
Chapter 7 ................................................................................................................................. 9
Chapter 8 ............................................................................................................................... 10
Chapter 9 ............................................................................................................................... 11
Chapter 10 ............................................................................................................................. 12
Chapter 11 ............................................................................................................................. 14
Chapter 12 ............................................................................................................................. 15
Chapter 13 ............................................................................................................................. 16
Chapter 14 ............................................................................................................................. 17
Chapter 15 ............................................................................................................................. 18
Chapter 16 ............................................................................................................................. 19
Chapter 17 ............................................................................................................................. 21
Chapter 18 ............................................................................................................................. 22
Chapter 19 ............................................................................................................................. 23
Chapter 20 ............................................................................................................................. 23
Chapter 21 ............................................................................................................................. 24
Chapter 22 ............................................................................................................................. 25
Chapter 23 ............................................................................................................................. 27
Chapter 24 ............................................................................................................................. 28
Chapter 25 ............................................................................................................................. 29
Chapter 26 ............................................................................................................................. 30
Chapter 27 ............................................................................................................................. 31
Chapter 28 ............................................................................................................................. 32
Chapter 29 ............................................................................................................................. 34
Chapter 30 ............................................................................................................................. 35
Chapter 31 ............................................................................................................................. 36
Chapter 32 ............................................................................................................................. 37
Chapter 33 ............................................................................................................................. 38
Chapter 34 ............................................................................................................................. 39
Chapter 35 ............................................................................................................................. 41
Chapter 36 ............................................................................................................................. 42
1|Page

,Chapter 37 ............................................................................................................................. 43
Chapter 38 ............................................................................................................................. 45
Chapter 39 ............................................................................................................................. 46
Chapter 40 ............................................................................................................................. 47
Chapter 41 ............................................................................................................................. 48
Chapter 42 ............................................................................................................................. 49
Chapter 43 ............................................................................................................................. 50
Chapter 44 ............................................................................................................................. 51
Chapter 45 ............................................................................................................................. 52
Chapter 46 ............................................................................................................................. 54
Chapter 47 ............................................................................................................................. 56


Chapter 1
1 Figure 1.6 1: C; 2: F; 3: A; 4: B; 5: D; 6: E. The original hypothesis is incorrect, as the
coffeemaker works when plugged into the outlet. Alternative hypotheses include that the
toaster might be broken or that the toaster wasn't turned on.
3 Figure 1.16 Communities exist within populations which exist within ecosystems.
4B
6D
8C
10 C
12 B
14 D
16 Answers will vary, but should apply the steps of the scientific method. One
possibility could be a car which doesn’t start. The hypothesis could be that the car
doesn’t start because the battery is dead. The experiment would be to change the
battery or to charge the battery and then check whether the car starts or not. If it starts,
the problem was due to the battery, and the hypothesis is accepted.
18 Answers will vary. Topics that fall inside the area of biological study include how
diseases affect human bodies, how pollution impacts a species’ habitat, and how plants
respond to their environments. Topics that fall outside of biology (the “study of life”)
include how metamorphic rock is formed and how planetary orbits function.
20 Answers will vary. Layers of sedimentary rock have order but are not alive.
Technology is capable of regulation but is not, of itself, alive.
22 During your walk, you may begin to perspire, which cools your body and helps your
body to maintain a constant internal temperature. You might also become thirsty and
pause long enough for a cool drink, which will help to restore the water lost during
perspiration.
Chapter 2

1 Figure 2.3 Carbon-12 has six neutrons. Carbon-13 has seven neutrons.
2|Page

,3. Figure 2.24 C

3 A

6 C

8 D

10C

12

D

14 Ionic bonds are created between ions. The electrons are not shared between the
atoms, but rather are associated more with one ion than the other. Ionic bonds are
strong bonds, but are weaker than covalent bonds, meaning it takes less energy to
break an ionic bond compared with a covalent one.

16 Buffers absorb the free hydrogen ions and hydroxide ions that result from chemical
reactions. Because they can bond these ions, they prevent increases or decreases in
pH. An example of a buffer system is the bicarbonate system in the human body. This
system is able to absorb hydrogen and hydroxide ions to prevent changes in pH and
keep cells functioning properly.

18 Carbon is unique and found in all living things because it can form up to four
covalent bonds between atoms or molecules. These can be nonpolar or polar
covalent bonds, and they allow for the formation of long chains ofcarbon molecules that
combine to form proteins and DNA.
Chapter 3

1 Figure 3.5 Glucose and galactose are aldoses. Fructose is a ketose.

3 Figure 3.33 Adenine is larger than cytosine and will not be able to base pair properly
with the guanine on the opposing strand. This will cause the DNA to bulge. DNA repair
enzymes may recognize the bulge and replace the incorrect nucleotide.

4C

6A

8D

10 B

12 D

14 C


3|Page

, 16 B

18 C

20 C

21 Biological macromolecules are organic because they contain carbon.

23 Amino acids can be linked into long chains through condensation reactions. One of
the hydrogen atoms bonded to the nitrogen atom of an amino acid reacts with the –OH
group attached to the terminal carbon on another amino acid. Since both ends of the
molecule can participate in condensation reactions, peptide bonds can be made in
both directions to create a long amino acid chain.

25 The β 1-4 glycosidic linkage in cellulose cannot be broken down by human digestive
enzymes. Herbivores such as cows, koalas, and buffalos are able to digest grass that is
rich in cellulose and use it as a food source because bacteria and protists in their
digestive systems, especially in the rumen, secrete the enzyme cellulase. Cellulases
can break down cellulose into glucose monomers that can be used as an energy
source by the animal.

27 Fat serves as a valuable way for animals to store energy. It can also provide
insulation. Waxes can protect plant leaves and mammalian fur from getting wet.
Phospholipids and steroids are important components of animal cell membranes, as
well as plant, fungal, and bacterial membranes.

29 Fats have a higher energy density than carbohydrates (averaging 9kcal/gram versus
4.3kcal/gram respectively). Thus, on a per gram basis, more energy can be stored in
fats than can be stored in carbohydrates. Additionally, fats are packaged into spherical
globules to minimize interactions with the water-based plasma membrane, while
glycogen is a large branched carbohydrate that cannot be compacted for storage.

31 A change in gene sequence can lead to a different amino acid being added to a
polypeptide chain instead of the normal one. This causes a change in protein structure
and function. For example, in sickle cell anemia, the hemoglobin β chain has a single
amino acid substitution—the amino acid glutamic acid in position six is substituted by
valine. Because of this change, hemoglobin molecules form aggregates, and the disc-
shaped red blood cells assume a crescent shape, which results in serious health
problems.
33 The protein must form a channel in the plasma membrane that allows water into the
cell since water cannot cross the plasma membrane by itself. Since aquaporins are
embedded in the plasma membrane and connect with both the intracellular and
extracellular spaces, it must be amphipathic like the plasma membrane. The top and
bottom of the protein must contain charged or polar amino acids (hydrophilic) to interact
with the aqueous environments. The exterior transmembrane region must contain non-
polar amino acids (hydrophobic) that can interact with the phospholipid tail. However,
the inside of this channel must contain hydrophilic amino acids since they will interact
with the traveling water molecules.


4|Page

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