High School Science Investigation and Experimentation Standard
Questions at the end of standards-based textbook readings and/or activities cited in the right-hand column after each standard/benchmark can be considered as potential standards based assessment questions for quarter "mid-terms" or semester "end-of-term" finals.· YELLOW is used to draw attention to core instructional vocabulary. BLUE is used to draw attention to instructional "experiences" that students should have. GREEN is used to draw attention to expected student opportunities (some requiring the application student initiated metacognitive skills) based on state framework suggestions. RED is used to draw attention to issues that might affect the scope and sequence of how the standard based material is presented. PINK is used to draw attentions to items that can be used for "cross-curricular" integration of "Language Arts" standard-based items. GRAY is used to draw attentions to items that can be used for "cross-curricular" integration of "Mathematics" standard-based items. Notations like "Q 2" beside a standard or benchmark mean that the standard or benchmark in question will be covered during the 2nd Quarter. L means late in the quarter and E means early in the quarter. The "Content Standard Summary " and annotations after each standard and benchmark are from the California Science Framework . A * benchmark means it is not considered an "Essential Standard" ((Standards considered "essential" are those that are included in the state CST blueprint for a given subject area test). "(13% - 8 items) " means that 13% or 8 questions on the HS Life Sciences CSS CRT have been written using framework descriptions for this standard and its benchmarks (Bio/LS CST Blueprint, 2005) NE - Considered a Non-Essential Standard (Standards considered "essential" are those that are included in the state CST blueprint for a given subject area test)- Resources used:
Course: Introduction to the Principle of BiologyText: Biology: The Dynamics of Life, Glencoe McGraw-Hill, 2002Criteria: California Science Content Standard for High School Life Sciences/ BiologyMetacognition: means "thinking about thinking". Metacognition refers to higher order thinking involving the "learners" active control over the cognitive processes engaged in learning. It entails planning how to approach a given learning task, monitoring their personal comprehension, and evaluating their progress toward the completion of that task. Put simply, metacognition is a buzzword in educational psychology for thinking before doing something. Metacognitive strategies are memorable plans or approaches that students use to problem-solve. These strategies include the student’s thinking as well as their physical actions. Common metacognitive strategies include: mnemonics, in the form of easy to remember phrases or through pictures that are easy to recall, asking for clarification, etc.
- Q 2 |
g. -the role of the mitochondria in making stored chemical bond energy available to cells by completing the breakdown of glucose to carbon dioxide. |
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Mitochondria consist of a matrix where three-carbon fragments originating from carbohydrates are broken down (to CO2 and water) and of the cristae where ATP is produced. Cell respiration occurs in a series of reactions in which fats, proteins, and carbohydrates, mostly glucose, are broken down to produce carbon dioxide, water, and energy. Most of the energy from cell respiration is converted into ATP, a substance that powers most cell activities. |
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- Q 1 - 2 |
h. most macromolecules (polysaccharides, nucleic acids, proteins, lipids) in cells and organisms are synthesized from a small collection of simple precursors. |
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Many of the large carbon compound molecules necessary for life (e.g., polysaccharides, nucleic acids, proteins, and lipids) are polymers of smaller monomers. Polysaccharides are composed of monosaccharides; proteins are composed of amino acids; lipids are composed of fatty acids, glycerol, and other components; and nucleic acids are composed of nucleotides. |
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NE- Q 1 - 2 |
i.* how chemiosmotic gradients in the mitochondria and chloroplast store energy for ATP production. |
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Enzymes called ATP synthase, located within the thylakoid membranes in chloroplasts and cristae membranes in mitochondria, synthesize most ATP within cells. The thylakoid and cristae membranes are impermeable to protons (H+) except at pores that are coupled with the ATP synthase. The potential energy of the proton concentration gradient drives ATP synthesis as the protons move through the ATP synthase pores. The proton gradient is established by energy furnished by a flow of electrons (e-) passing through the electron transport system located within these membranes. |
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NE- Q 1 - 2 |
j* how eukaryotic cells are given shape and internal organization by a cytoskeleton and/or cell wall. |
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The cytoskeleton, which gives shape to and organizes eukaryotic cells, is composed of fine protein threads called microfilaments and thin protein tubes called microtubules. Cilia and flagella are composed of microtubules arranged in the 9 + 2 arrangement, in which nine pairs of microtubules surround two single microtubules. The rapid assembly and disassembly of microtubules and microfilaments and their capacity to slide past one another enable cells to move, as observed in white blood cells and amoebae, and also account for movement of organelles within the cell. Students can observe prepared slides of plant mitosis in an onion root tip to see the microtubules that make up the spindle apparatus. Prepared slides of white fish blastula reveal animal spindle apparatus and centrioles, both of which are composed of microtubules. |
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Students should know that organisms reproduce offspring of their own kind (specific biogenesis) and that organisms of the same species resemble each other. Students have been introduced to the idea that some characteristics can be passed from parents to offspring and that individual variations appear among offspring and in the broader population. Understanding genetic variation requires mastery of the fundamentals of sex cell formation and the steps to reorganize and redistribute genetic material during defined stages in the cell cycle. Students should understand the difference between asexual cell reproduction (mitosis) and the formation of male or female gamete cells (meiosis). Sexual reproduction initially requires the production of haploid eggs and haploid sperm, a process occurring in humans within the female ovary and the male testis. These haploid cells unite in fertilization and produce the diploid zygote, or fertilized cell. The mechanisms involved in synapsis and movement of chromosomes during meiosis bring about the halving of the chromosome numbers for the production of the haploid male or female gamete cells from the original diploid parent cell and different combinations of parental genes. The exchange of chromosomal segments between homologous chromosomes (crossing over) revises the association of genes on the chromosomes and contributes to increased diversity. Any change in genetic constitution through mutation, crossing over, or chromosome assortment during meiosis promotes genetic variation in a population. |
Chapter and section Numbers (For Biology: The Dynamics of Life, 2002, Glencoe/McGraw-Hill) |
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Genetics (30% of CST, 18 items) - Q 2, 3 [ 6 items] 2. Mutation and sexual reproduction lead to genetic variation in a population. As a basis for understanding this concept, students know: |
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- Q 2L - 3 |
a. meiosis is an early step in sexual reproduction in which the pairs of chromosomes separate and segregate randomly during cell division to produce gametes containing one chromosome of each type |
Chapter 10.2 BioDigest 369 |
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Haploid gamete production through meiosis involves two cell divisions. During meiosis prophase I, the homologous chromosomes are paired, a process that abets the exchange of chromosome parts through breakage and reunion. The second meiotic division parallels the mechanics of mitosis except that this division is not preceded by a round of DNA replication; therefore, the cells end up with the haploid number of chromosomes. (The nucleus in a haploid cell contains one set of chromosomes.) Four haploid nuclei are produced from the two divisions that characterize meiosis, and each of the four resulting cells has different chromosomal constituents (components). In the male all four become sperm cells. In the female only one becomes an egg, while the other three remain small degenerate polar bodies and cannot be fertilized. Chromosome models can be constructed and used to illustrate the segregation taking place during the phases of mitosis (covered initially in Standard 1.e for grade seven in Chapter 4) and meiosis. Commercially available optical microscope slides also show cells captured in mitosis (onion root tip) or meiosis (Ascaris blastocyst cells), and computer and video animations are also available. |
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- Q 2L - 3E |
b. - only certain cells in a multicellular organism undergo meiosis |
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Only special diploid cells, called spermatogonia in the testis of the male and oogonia in the female ovary, undergo meiotic divisions to produce the haploid sperm and haploid eggs. |
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- Q 2L - 3E |
c. -how random chromosome segregation explains the probability that a particular allele will be in a gamete. |
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The steps in meiosis involve random chromosome segregation, a process that accounts for the probability that a particular allele will be packaged in any given gamete. This process allows for genetic predictions based on laws of probability that pertain to genetic sortings. Students can create a genetic chart (Punnett Square(s)) and mark alternate traits on chromosomes, one expression coming from the mother and another expression coming from the father. Students can be shown that partitions of the chromosomes are controlled by chance (are random) and that separation (segregation) of chromosomes during karyokinesis (division of the nucleus) leads to the random sequestering of different combinations of chromosomes. |
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- Q 2L - 3E |
d. -new combinations of alleles may be generated in a zygote through fusion of male and female gametes (fertilization). |
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Once gametes are formed, the second half of sexual reproduction can take place. In this process a diploid organism is reconstituted from two haploid parts. When a sperm is coupled with an egg, a fertilized egg (zygote) is produced that contains the combined genotypes of the parents to produce a new allelic composition for the progeny. Genetic charts can be used to illustrate how new combinations of alleles may be present in a zygote through the events of meiosis and the chance union of gametes. Students should be able to read the genetic diploid karyotype, or chromosomal makeup, of a fertilized egg and compare the allelic composition of progeny with the genotypes and phenotypes of the parents. |
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- Q 2L - 3E |
e. -why approximately half of an individual's DNA sequence comes from each parent. |
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Chromosomes are composed of a single, very long molecule of double-stranded DNA and proteins. Genes are defined as segments of DNA that code for polypeptides (proteins). During fertilization half the DNA of the progeny comes from the gamete of one parent, and the other half comes from the gamete of the other parent. |
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- Q 2L |
f. -the role of chromosomes in determining an individual's sex. |
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The normal human somatic cell contains 46 chromosomes, of which 44 are pairs of homologous chromosomes and 2 are sex chromosomes. Females usually carry two X chromosomes, and males possess one X and a smaller Y chromosome. Combinations of these two sex chromosomes determine the sex of the progeny. |
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- Q 3E |
g. -how to predict possible combinations of alleles in a zygote from the genetic makeup of the parents. |
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When the genetic makeups of potential parents are known, the possible assortments of alleles in their gametes can be determined for each genetic locus. Two parental gametes will fuse during fertilization, and with all pair-wise combinations of their gametes considered, the possible genetic makeups of progeny can then be predicted. |
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Breeding of plants and animals has been an active technology for thousands of years, but the science of heredity is linked to the genetics pioneer Gregor Mendel. He studied phenotypic traits of various plants, especially those of peas. (A phenotypic trait is the physical appearance of a trait in an organism). From the appearance of these traits in different generations of growth, he was able to infer their genotypes (the genetic makeup of an organism with respect to a trait) and to speculate about the genetic makeup and method of transfer of the hereditary units from one generation to the next. (Probability analysis is now used to predict probable progeny phenotypes from various parental genetic crosses.) The genetic basis for Mendel's laws of segregation and independent assortment is apparent from genetic outcomes of crosses. |
Chapter and Section Numbers (For Biology: The Dynamics of Life, 2002, Glencoe/McGraw-Hill) |
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- Q 2, 3 [ 3 items] 3. A multicellular organism develops from a single zygote, and its phenotype depends on its genotype, which is established at fertilization. As a basis for understanding this concept, students know: |
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- Q 3 |
a. - how to predict the probable outcome of phenotypes in a genetic cross from the genotypes of the parents and mode of inheritance (autosomal or X-linked, dominant or recessive). |
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Monohybrid crosses, including autosomal dominant alleles, autosomal recessive alleles, incomplete dominant alleles, and X-linked alleles, can be used to indicate the parental genotypes and phenotypes. The possible gametes derived from each parent are based on genotypic ratios and can be used to predict possible progeny. The predictive (probabilistic) methods for determining the outcome of genotypes and phenotypes in a genetic cross can be introduced by using Punnett Squares and probability mathematics. Teachers should review the process of writing genotypes and help students translate genotypes into phenotypes. Teachers should emphasize dominant, recessive, and incomplete dominance as the students advance to an explanation of monohybrid crosses illustrating human conditions characterized by autosomal recessive alleles, such as albinism, cystic fibrosis, Tay-Sachs, and phenylketonuria (PKU). These disorders can be contrasted with those produced by possession of just one autosomal dominant allele, conditions such as Huntington disease, dwarfism, and neurofibromatosis. This basic introduction can be followed with examples of incomplete dominance, such as seen in the comparisons of straight, curly, and wavy hair or in the expression of intermediate flower colors in snapdragon plants. Sex-linked characteristics that are found only on the X chromosome should also be considered, and students should reflect on how this mode of transmission can cause the exclusive or near exclusive appearance in males of color blindness, hemophilia, fragile-X syndrome, and sex-linked muscular dystrophy. |
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- Q 3 |
b. -the genetic basis for Mendel's laws of segregation and independent assortment. |
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Mendel deduced that for each characteristic, an organism inherits two genes, one from each parent. When the two alleles differ, the dominant allele is expressed, and the recessive allele remains hidden. Two genes or alleles separate (segregate) during gamete production in meiosis, resulting in the sorting of alleles into separate gametes (the law of segregation). Students can be shown how to diagram Mendel's explanation for how a trait present in the parental generation can appear to vanish in the first filial (F1) generation of a monohybrid cross and then reappear in the following second filial (F2) generation. Students should be told that alternate versions of a gene at a single locus are called alleles. Students should understand Mendel's deduction that for each character, an organism inherits two genes, one from each parent. From this point students should realize that if the two alleles differ, the dominant allele, if there is one, is expressed, and the recessive allele remains hidden. Students should recall that the two genes, or alleles, separate (segregate) during gamete production in meiosis and that this sorting of alleles into separate gametes is the basis for the law of segregation. This law applies most accurately when genes reside on separate chromosomes that segregate out at random, and it often does not apply or is a poor predictor for combinations and frequencies of genes that reside on the same chromosome. Students can study various resources that describe Mendel's logic and build models to illustrate the laws of segregation and independent assortment. |
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NE- Q 3 |
c.* -how to predict the probable mode of inheritance from a pedigree diagram showing phenotypes. |
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Students should be taught how to use a pedigree diagram showing phenotypes to predict the mode of inheritance. |
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NE-Not addressed |
d.* - how to use data on frequency of recombination at meiosis to estimate genetic distances between loci, and to interpret genetic maps of chromosomes. |
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Students should be able to interpret genetic maps of chromosomes and manipulate genetic data by using standard techniques to relate recombination at meiosis to estimate genetic distances between loci. |
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- Q 1 - 3 |
a. - the general pathway by which ribosomes synthesize proteins, using tRNAs to translate genetic information in mRNA. |
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DNA does not leave the cell nucleus, but messenger RNA (mRNA), complementary to DNA, carries encoded information from DNA to the ribosomes (transcription) in the cytoplasm. (The ribosomes translate mRNAs to make protein.) Freely floating amino acids within the cytoplasm are bonded to specific transfer RNAs (tRNAs) that then transport the amino acid to the mRNA now located on the ribosome. As a ribosome moves along the mRNA strand, each mRNA codon, or sequence of three nucleotides (triplet) specifying the insertion of a particular amino acid, is paired in sequence with the anticodon of the tRNA that recognizes the sequence. Each amino acid is added, in turn, to the growing polypeptide at the specified position. After learning about transcription and translation through careful study of expository texts, students can simulate the processes on paper or with representative models. Computer software and commercial videos are available that illustrate animated sequences of transcription and translation. |
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- Q 3 |
b. how to apply the genetic coding rules to predict the sequence of amino acids from a sequence of codons in RNA. |
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The sequence of amino acids in protein is provided by the genetic information found in DNA. In prokaryotes, mRNA transcripts of a coding sequence are copied from the DNA as a single contiguous sequence. In eukaryotes, the initial RNA transcript, while in the nucleus, is composed of exons, sequences of nucleotides that carry useful information for protein synthesis, and introns, sequences that do not. Before leaving the nucleus, the initial transcript is processed to remove introns and splice exons together. The processed transcript, then properly called mRNA and carrying the appropriate codon sequence for a protein, is transported from the nucleus to the ribosome for translation. Each mRNA has sequences, called codons, that are decoded three nucleotides at a time. Each codon specifies the addition of a single amino acid to a growing polypeptide chain. A start codon signals the beginning of the sequence of codons to be translated, and a stop codon ends the sequence to be translated into protein. Students can write out mRNA sequences with start and stop codons from a given DNA sequence and use a table of the genetic code to predict the primary sequences of proteins. |
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- Q 3 |
c. -how mutations in the DNA sequence of a gene may or may not affect the expression of the gene, or the sequence of amino acids in an encoded protein. |
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Mutations are permanent changes in the sequence of nitrogen-containing bases in DNA (see Standard 5.a in this section for details on DNA structure and nitrogen bases). Mutations occur when base pairs are incorrectly matched (e.g., A bonded to C rather than A bonded to T) and can, but usually do not, improve the product coded by the gene. Inserting or deleting base pairs in an existing gene can cause a mutation by changing the codon reading frame used by a ribosome. Mutations that occur in somatic, or nongerm, cells are often not detected because they cannot be passed on to offspring. They may, however, give rise to cancer or other undesirable cellular changes. Mutations in the germline can produce functionally different proteins that cause such genetic diseases as Tay-Sachs, sickle cell anemia, and Duchenne muscular dystrophy. |
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| - Q 3 |
d. -specialization of cells in multicellular organisms is usually due to different patterns of gene expression rather than to differences of the genes themselves. |
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Gene expression is a process in which a gene codes for a product, usually a protein, through transcription and translation. Nearly all cells in an organism contain the same DNA, but each cell transcribes only that portion of DNA containing the genetic information for proteins required at that specific time by that specific cell. The remainder of the DNA is not expressed. Specific types of cells may produce specific proteins unique to that type of cell. |
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- Q 3 |
e. -proteins can differ from one another in the number and sequence of amino acids. |
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Protein molecules vary from about 50 to 3,000 amino acids in length. The types, sequences, and numbers of amino acids used determine the type of protein produced. |
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NE- Q 2L - 3E |
f.* -why proteins having different amino acid sequences typically have different shapes and chemical properties. |
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The 20 different protein-making amino acids have the same basic structure: an amino group; an acidic (carboxyl) group; and an R, or radical group (Chemistry Standard 10, "Organic and Biochemistry," ). The protein is formed by the amino group of one amino acid linking to the carboxyl group of another amino acid. This bond, called the peptide bond, is repeated to form long molecular chains with the R groups attached along the polymer backbone. The properties of these amino acids vary from one another because of both the order and the chemical properties of these R groups. Typically, the long protein molecule folds on itself, creating a three-dimensional structure related to its function. Structure, for example, may allow a protein to be a highly specific catalyst, or enzyme, able to position and hold other molecules. The R group of an amino acid consists of atoms that may include carbon, hydrogen, nitrogen, oxygen, and sulfur, depending on the amino acid. Amino acids containing sulfur sometimes play an important role of cross-linking and stabilizing polymer chains. Because of their various R groups, different amino acids vary in their chemical and physical properties, such as solubility in water, electrical charge, and size. These differences are reflected in the unique structure and function of each type of protein. |
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- Q 1 - 3 |
a. -the general structures and functions of DNA, RNA, and protein. |
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Nucleic acids are polymers composed of monomers called nucleotides. Each nucleotide consists of three subunits: a five-carbon pentose sugar, a phosphoric acid group, and one of four nitrogen bases. (For DNA these nitrogen bases are adenine, guanine, cytosine, or thymine.) DNA and RNA differ in a number of major ways. A DNA nucleotide contains a deoxyribose sugar, but RNA contains ribose sugar. The nitrogen bases in RNA are the same as those in DNA except that thymine is replaced by uracil. RNA consists of only one strand of nucleotides instead of two as in DNA. The DNA molecule consists of two strands twisted around each other into a double helix resembling a ladder twisted around its long axis. The outside, or uprights, of the ladder are formed by the two sugar-phosphate backbones. The rungs of the ladder are composed of pairs of nitrogen bases, one extending from each upright. In DNA these nitrogen bases always pair so that T pairs with A, and G pairs with C. This pairing is the reason DNA acts as a template for its own replication. RNA exists in many structural forms, many of which play different roles in protein synthesis. The mRNA form serves as a template during protein synthesis, and its codons are recognized by aminoacylated tRNAs. Protein and rRNA makeup the structure of the ribosome. Proteins are polymers composed of amino acid monomers (Chemistry Standard 10). Different types of proteins function as enzymes and transport molecules, hormones, structural components of cells, and antibodies that fight infection. Most cells in an individual organism carry the same set of DNA instructions but do not use the entire DNA set all the time. Only a small amount of the DNA appropriate to the function of that cell is expressed. Genes are, therefore, turned on or turned off as needed by the cell, and the products coded by these genes are produced only when required. |
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- Q 3 |
b. -how to apply base-pairing rules to explain precise copying of DNA during semi-conservative replication, and transcription of information from DNA into mRNA. |
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Enzymes initiate DNA replication by unzipping, or unwinding, the double helix to separate the two parental strands. Each strand acts as a template to form a complementary daughter strand of DNA. The new daughter strands are formed when complementary new nucleotides are added to the bases of the nucleotides on the parental strands. The nucleotide sequence of the parental strand dictates the order of the nucleotides in the daughter strands. One parental strand is conserved and joins a newly synthesized complementary strand to form the new double helix; this process is called semi-conservative replication. DNA replication is usually initiated by the separation of DNA strands in a small region to make a "replication bubble" in which DNA synthesis is primed. The DNA strands progressively unwind and are replicated as the replication bubble expands, and the two forks of replication move in opposite directions along the chromosome. At each of the diverging replication forks, the strand that is conserved remains a single, continuous "leading" strand, and the other "lagging" complementary strand is made as a series of short fragments that are subsequently repaired and ligated together. Students may visualize DNA by constructing models, and they can simulate semiconservative replication by tracing the synthesis of the leading and lagging strands. The critical principles to teach with this activity are that two doublestranded DNA strands are the product of synthesis, that the process is semiconservative, that the antiparallel orientation of the strands requires repeated reinitiation on the lagging strand, and that the only information used during synthesis is specified by the base-pairing rules. RNA is produced from DNA when a section of DNA (containing the nucleotide sequence required for the production of a specific protein) is transcribed. Only the template side of the DNA is copied. RNA then leaves the nucleus and travels to the cytoplasm, where protein synthesis takes place. |
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- Q 3 Use a Video |
c. -how genetic engineering (biotechnology) is used to produce novel biomedical and agricultural products. |
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Recombinant DNA contains DNA from two or more different sources. Bacterial plasmids and viruses are the two most common vectors, or carriers, by which recombinant DNA is introduced into a host cell. Restriction enzymes provide the means by which researchers cut DNA at desired locations to provide DNA fragments with "sticky ends." Genes, once identified, can be amplified either by cloning or by polymerase chain reactions, both of which produce large numbers of copies. The recombinant cells are then grown in large fermentation vessels, and their products are extracted from the cells (or from the medium if the products are secreted) and purified. Genes for human insulin, human growth hormone, blood clotting factors, and many other products have been identified and introduced into bacteria or other microorganisms that are then cultured for commercial production. Some agricultural applications of this technology are the identification and insertion of genes to increase the productivity of food crops and animals and to promote resistance to certain pests and herbicides, robustness in the face of harsh environmental conditions, and resistance to various viruses. Students can model the recombinant DNA process by using paper models to represent eukaryotic complementary DNA (cDNA), the activity of different restriction enzymes, and ligation into plasmid DNA containing an antibiotic resistance gene and origin of DNA replication. To manipulate the modeled DNA sequences, students can use scissors (representing the activity of restriction enzymes) and tape (representing DNA ligase). If both strands are modeled on a paper tape, students can visualize how, in many cases, restriction enzymes make staggered cuts that generate "sticky ends" and how the ends must be matched during ligation. |
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NE- Q 3 Use a Video |
d.*-how basic DNA technology (restriction digestion by endonucleases, gel electrophoresis, ligation, and transformation) is used to construct recombinant DNA molecules. |
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In recombinant DNA technology DNA is isolated and exchanged between organisms to fulfill a specific human purpose. The desired gene is usually identified and extracted by using restriction enzymes, or endonucleases, to cut the DNA into fragments. Restriction enzymes typically cut palindromic portions of DNA, which read the same forward and backward, in ways that form sticky complementary ends. DNA from different sources, but with complementary sticky ends, can be joined by the enzyme DNA ligase, thus forming recombinant DNA. DNA fragments of varying lengths can be separated from one another by gel electrophoresis. In this process the particles, propelled by an electric current, are moved through an agarose gel. Depending on the size, shape, and electrical charge of the particles, they will move at different rates through the gel and thus form bands of particles of similar size and charge. With appropriate staining, the various DNA fragments can then be visualized and removed for further analysis or recombination. |
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NE- Q 3 Use a Video |
e.* -how exogenous DNA can be inserted into bacterial cells in order to alter their genetic makeup and support expression of new protein products. |
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Bacteria can be induced to take up recombinant plasmids, a process called DNA transformation, and the plasmid is replicated as the bacteria reproduce. Recombinant bacteria can be grown to obtain billions of copies of the recombinant DNA. Commercially available kits containing all the necessary reagents, restriction enzymes, and bacteria are available for experiments in plasmid DNA transformation. Although the reagents and equipment can be expensive, various California corporations and universities have programs to make the cost more affordable, sometimes providing reagents and lending equipment. Students should know that DNA transformation is a natural process and that horizontal DNA transfer is common in the wild. An example of how humans have manipulated genetic makeup is through the selective breeding of pets and of agricultural crops. |
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- Q 1- 2 |
b. -how to analyze changes in an ecosystem resulting from changes in climate, human activity, introduction of non-native species, or changes in population size. |
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Analysis of change can help people to describe and understand what is happening in a natural system and, to some extent, to control or influence that system. Understanding different kinds of change can help to improve predictions of what will happen next. Changes in ecosystems often manifest themselves in predictable patterns of climate, seasonal reproductive cycles, population cycles, and migrations. However, unexpected disturbances caused by human intervention or the introduction of a new species, for example, may destabilize the often complex and delicate balance in an ecosystem. Analyzing changes in an ecosystem can require complex methods and techniques because variation is not necessarily simple and may be interrelated with changes or trends in other factors. Rates and patterns of change, including trends, cycles, and irregularities, are essential features of the living world and are useful indicators of change that can provide data for analysis. Often it is important to analyze change over time, a process called longitudinal analysis. |
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- Q 1- 2 |
c. -how fluctuations in population size in an ecosystem are determined by the relative rates of birth, immigration, emigration, and death. |
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Fluctuations in the size of a population are often difficult to measure directly but may be estimated by measuring the relative rates of birth, death, immigration, and emigration in a population. The number of deaths and emigrations over time will decrease a population's size, and the number of births and immigrations over time will increase it. Comparing rates for death and emigration with those for birth and immigration will determine whether the population shows a net growth or a decline over time. |
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- Q 1 - 4 |
d. -how water, carbon, and nitrogen cycle between abiotic resources and organic matter in the ecosystem and how oxygen cycles via photosynthesis and respiration. |
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Living things depend on nonliving things for life. At the organism level living things depend on natural resources, and at the molecular level, they depend on chemical cycles. Water, carbon, nitrogen, phosphorus, and other elements are recycled back and forth between organisms and their environments. Water, carbon, and nitrogen are necessary for life to exist. These chemicals are incorporated into plants (producers) by photosynthesis and nitrogen fixation and used by animals (consumers) for food and protein synthesis. Chemical recycling occurs through respiration, the excretion of waste products and, of course, the death of organisms. |
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- Q 1 - 4 |
e. -a vital part of an ecosystem is the stability of its producers and decomposers. |
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An ecosystem's producers (plants and photosynthetic microorganisms) and decomposers (fungi and microorganisms) are primarily responsible for the productivity and recycling of organic matter, respectively. Conditions that threaten the stability of producer and decomposer populations in an ecosystem jeopardize the availability of energy and the capability of matter to recycle in the rest of the biological community. To study the interaction between producers and decomposers, students can set up a closed or restricted ecosystem, such as a worm farm, a composting system, a terrarium, or an aquarium. |
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- Q 1 - 2 |
f. -at each link in a food web, some energy is stored in newly made structures but much is dissipated into the environment as heat and this can be represented in a food pyramid. |
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The energy pyramid illustrates how stored energy is passed from one organism to another. At every level in a food web, an organism uses energy metabolically to survive and grow, but much is released as heat, usually about 90 percent. At every link in a food web, energy is transferred to the next level, but typically only 10 percent of the energy from the previous level is passed on to the consumer. |
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| NE-Not addressed |
g.* -how to distinguish between the accommodation of an individual organism to its environment and the gradual adaptation of a lineage of organisms through genetic change. |
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Living organisms may adapt to changing environments through nongenetic changes in their structure, metabolism, or behavior or through natural selection of favorable combinations of alleles governing any or all of these processes. Genetic and behavioral adaptations are sometimes difficult to identify or to distinguish without studying the organism over a long time. Physical changes are slow to develop in most organisms, requiring careful measurements over many years. Examining fossil ancestors of an organism may help provide clues for detecting adaptation through genetic change. Genetic change can institute behavioral changes, making it all the more complicated to determine whether a change is solely a behavioral accommodation to environmental change. Through the use of print and online resources in library-media centers, students can research the effects of encroaching urbanization on undeveloped land and consider the effects on specific species, such as the coyote (not endangered) and the California condor (endangered). Such examples can illustrate how some organisms adapt to their environments through learned changes in behavior, and others are unsuccessful in learning survival skills. Over a long time, organisms can also adapt to changing environments through genetic changes, some of which may include genetically determined changes in behavior. Such changes may be difficult to recognize because a long time must elapse before the changes become evident. Studies of the origins of desert pup fish or blind cave fish may help students understand how gradual genetic changes in an organism lead to adaptations to changes in its habitat. |
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From the individual cell to the total organism, each functioning unit is organized according to homeostasis, or how the body and its parts deal with changing demands while maintaining a constant internal environment. In 1859 noted French physiologist Claude Bernard described the difference between the internal environment of the cells and the external environment in which the organism lives. Organisms are shielded from the variations of the external environment by the "constancy of the internal milieu." This "steady state" refers to the dynamic equilibrium achieved by the integrated functioning of all the parts of the organism. American physiologist Walter Cannon called this phenomenon homeostasis, which means "standing still." All organ systems of the human body contribute to homeostasis so that blood and tissue constituents and values stay within a normal range. Students will need supportive review of the major systems of the body and of the organ components of those systems (see Standard Set 2, "Life Sciences," for grade five in Chapter 3 and Standard Set 5, "Structure and Function in Living Systems," for grade seven in Chapter 4). As the prime coordinators of the body's activities, the nervous and endocrine systems must be examined and their interactive roles clearly defined. |
Chapter and Section Numbers (For Biology: The Dynamics of Life, 2002, Glencoe/McGraw-Hill) |
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| Physiology (18.3
of CRT : 11 items]- Q 3L, 4 [
6 items] 9. As a result of the coordinated structures and functions of organ systems,
the internal environment of the human body remains relatively stable
(homeostatic), despite changes
in the outside environment. As a basis for understanding this concept,
students know: |
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- Q 4 |
a. -how the complementary activity of major body systems provides cells with oxygen and nutrients, and removes toxic waste products such as carbon dioxide. |
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The digestive system delivers nutrients (e.g., glucose) to the circulatory system. Oxygen molecules move from the air to the alveoli of the lungs and then to the circulatory system. From the circulatory system glucose and oxygen molecules move from the capillaries into the cells of the body where cellular respiration occurs. During cellular respiration these molecules are oxidized into carbon dioxide and water, and energy is trapped in the form of ATP. The gas exchange process is reversed for the removal of carbon dioxide from its higher concentration in the cells to the circulatory system and, finally, to its elimination by exhalation from the lungs. The concentration of sugar in the blood is monitored, and students should know that sugar can be stored or pulled from reserves (glycogen) in the liver and muscles to maintain a constant blood sugar level. Amino acids contained in proteins can also serve as an energy source, but first the amino acids must be deaminated, or chemically converted, in the liver, producing ammonia (a toxic product), which is converted to water-soluble urea and excreted by the kidneys. Teachers should emphasize that all these chemicals are transported by the circulatory system and the cells. Organs at the final destination direct these chemicals to their exit from the circulatory system. |
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- Q 1- 4 |
b. -how the nervous system mediates communication between different parts of the body and interactions with the environment. |
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An individual becomes aware of the environment through the sense organs and other body receptors (e.g., by allowing for touch, taste, and smell and by collecting information about temperature, light, and sound). The body reflexively responds to external stimuli through a reflex arc (see Standard 9.e in this section). (A reflex arc is the pathway along the central nervous system where an impulse must travel to bring about a reflex; e.g., sneezing or coughing.) Students can examine the sense organs, identify other body receptors that make them aware of their environment, and see ways in which the body reflexively responds to an external stimulus through a reflex arc. Hormones work in conjunction with the nervous system, as shown, for example, in the digestive system, where insulin released from the pancreas into the blood regulates the uptake of glucose by muscle cells. The pituitary master gland produces growth hormone for controlling height. Other pituitary hormones have specialized roles (e.g., follicle-stimulating hormone [FSH] and luteinizing hormone [LH] control the gonads, thyroid-stimulating hormone [TSH] controls the thyroid, and adrenocorticotropic hormone [ACTH] regulates the formation of glucocorticoids by the adrenal cortex). This master gland is itself controlled by the hypothalamus of the brain. |
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- Q 1- 4 |
c. -how feedback loops in the nervous and endocrine systems regulate conditions within the body. |
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Feedback loops are the means through which the nervous system uses the endocrine system to regulate body conditions. The presence or absence of hormones in blood brought to the brain by the circulatory system will trigger an attempt to regulate conditions in the body. To make feedback loops relevant to students, teachers can discuss the hormone leptin, which fat cells produce as they become filled with storage reserves. Leptin is carried by the blood to the brain, where it normally acts to inhibit the appetite center, an example of negative feedback. When fat reserves diminish, the concentration of leptin decreases, a phenomenon that in turn causes the appetite center in the brain to start the hunger stimulus and activate the urge to eat. |
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- Q 4 |
d. -the functions of the nervous system, and the role of neurons in transmitting electrochemical impulses. |
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Transmission of nerve impulses involves an electrochemical "action potential" generated by gated ion channels in the membrane that make use of the countervailing gradients of sodium and potassium ions across the membrane. Potassium ion concentration is high inside cells and low outside; sodium ion concentration is the opposite. The sodium and potassium ion concentration gradients are restored by an active transport system, a pump that exchanges sodium and potassium ions across the membrane and uses ATP hydrolysis as a source of free energy. The release of neurotransmitter chemicals from the axon terminal at the synapse may initiate an action potential in an adjacent neuron, propagating the impulse to a new cell. |
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- Q 4 |
e. -the roles of sensory neurons, interneurons, and motor neurons in sensation, thought, and response. |
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The pathways of impulses from dendrite to cell body to axon of sensory neurons, interneurons, and motor neurons link the chains of events that occur in a reflex action. Students should be able to diagram this pathway. Similar paths of neural connections lead to the brain, where the sensations become conscious and conscious actions are initiated in response to external stimuli. Students might also trace the path of the neural connections as the sensation becomes conscious and a response to the external stimulus is initiated. Students should also be able to identify gray and white matter in the central nervous system. |
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- Q 4 |
f.* -the individual functions and sites of secretion of digestive enzymes (amylases, proteases, nucleases, lipases), stomach acid, and bile salts. |
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To bring about digestion, secretions of enzymes are mixed with food (in the mouth and as the food proceeds from the mouth through the stomach and through the small intestines). For example, salivary glands and the pancreas secrete amylase enzymes that change starch into sugar. Stomach acid and gastric enzymes begin the breakdown of protein, a process that intestinal and pancreatic secretions continue. Lipase enzymes secreted by the pancreas break down fat molecules (which contain three fatty acids) to free fatty acids plus diglycerides (which contain two fatty acids) and monoglycerides (which contain one fatty acid). Bile secreted by the liver furthers the process of digestion, emulsifying fats and facilitating digestion of lipids. Students might diagram the digestive tract, labeling important points of secretion and tracing the pathways from digestion of starches, proteins, and other foods. They can then outline the role of the kidney nephron in the formation of urine and the role of the liver in glucogenesis and glycogenolysis (glucose balance) and in blood detoxification. |
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NE - Not addressed |
g.*-the homeostatic role of the kidneys in the removal of nitrogenous wastes, and of the liver in blood detoxification and glucose balance. |
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Microscopic nephrons within the kidney filter out body wastes, regulate water, and stabilize electrolyte levels in blood. The liver removes toxic materials from the blood, stores them, and excretes them into the bile. The liver also regulates blood glucose. |
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NE - Not addressed |
h.*- the cellular and molecular basis of muscle contraction, including the roles of actin, myosin, Ca+2, and ATP. |
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Controlled by calcium ions and powered by hydrolysis of ATP, actin and myosin filaments in a sarcomere generate movement in stomach muscles. Striated muscle fibers reflect the filamentous makeup and contraction state evidenced by the banding patterns of those fibers. A sketch of the sarcomere can be used to indicate the functions of the actin and myosin filaments and the role of calcium ions and ATP in muscle contraction. |
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NE - Not addressed |
i.*- how hormones (including digestive, reproductive, osmoregulatory) provide internal feedback mechanisms for homeostasis at the cellular level and in whole organisms. |
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Hormones act as chemical messengers, affecting the activity of neighboring cells or other target organs. Their movement can be traced from their point of origin to the target site. The feedback mechanism works to regulate the activity of hormones and promotes homeostasis. |
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