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Biology Essential Outcomes

Biology 1001: Essential Outcomes

Principles underlying evolution by natural selection

  • Mutations arise in a population randomly

    • Recombination in sexual reproduction during meiosis (crossing over)

  • If a mutation is favorable, the organism will survive and reproduce to pass on the allele

  • Over time, the frequency of this allele will rise in the population = evolution

Evidence supporting descent with modification from a common ancestor

  • Historical Biogeography

    • Studies of the world distribution of plants and animals

  • Comparative Morphology

    • Comparing anatomical structures of organisms (vestigial structures) and embryonic development similarities

  • Geology

    • Looking at fossils representing organisms

Characteristics of a scientific theory and the importance of falsifiability

  • Theories are testable hypotheses about the natural world

  • Must be falsifiable to be considered scientific

  • Must be objective, not mythical, cannot be a definition, can't be faith-based, and must be reasonably possible to test

Changes in amount of DNA throughout the cell cycle

  • G1: One copy of DNA

  • S: DNA is copied

  • G2: Two copies of DNA

  • M: prophase-metaphase (n=2, c=4) anaphase-telophase (n=2, c=2)

Main features of each stage of mitosis with respect to the cytoskeleton and the chromatin

  • Prophase

    • Chromatin condenses, nucleolus disappears, spindle (microtubules) begin forming and moving to poles, nuclear membrane breaks down

  • Pro-metaphase

    • Microtubules grow from centrosomes towards cell center, spindles attach to chromosome kinetochores

  • Metaphase

    • Spindle microtubules move chromosomes into alignment, chromosomes complete condensation

  • Anaphase

    • Sister chromatids separate and move along spindles using kinetochore motor, some spindles push each other and some pull chromosomes

  • Telophase

    • Spindle disassembles, nucleolus and nuclear envelope reappear

Cytokinesis

  • Cleavage furrow

    • Layer of microtubules stretches across spindle midpoint

    • A band of microfilaments (actin) forms in plasma membrane and tightens to squeeze off cell into two

  • Cell Plate

    • Layer of microtubules in the middle is covered in vesicles across the entire cell

    • Vesicles fuse together to make a new cell wall splitting the cell in half

Structure of a replication bubble

  • Origin of replication is in the middle

  • Replication fork unzips from this point in opposite directions

  • Leading strand (one RNA primer extended) and lagging strand (multiple RNA primers added in Okazaki fragments) for each side of the bubble

  • Linear chromosomes have many simultaneous bubbles, circular chromosomes have only one at a time

Relationship between DNA replication and metaphase chromosome structure

  • DNA has been replicated in Interphase and stays together as two sister chromatids up until Metaphase

  • Each chromosome in Metaphase contains two double helixes (extremely condensed and attached at a centromere)

Difference between DNA damage and mutation

  • Damage is a single-stranded change in the DNA

  • Mutations are any double-stranded change in the DNA sequence

  • Mutations may arise from initial damage and can be good or bad, but are necessary for evolution

Origin of various types of genomic variation

  • SNP's (Single Nucleotide Polymorphisms)

    • Caused by replication errors and tautomeric shifts

  • CNV's (Copy Number Variations)

    • Caused by uneven crossing over

  • In/Del

    • Caused by "slippage" when many of the same nitrogen base are next to each other in a sequence

  • Duplication, Inversion, Translocation, and Large Deletions

    • May occur due to ionizing radiation that creates reactive O2 that steal electrons and break chromosomes

    • Non-homologous end joining pastes the end back together and is highly mutagenic

  • Mobile elements

    • Insertion sequences, transposons, retrotransposons, and retroviruses exist and move throughout the genome

    • Cut and paste or copy and paste mechanisms without the enzyme transposase

    • Increase genetic variability

Main differences between meiosis and mitosis

  • Mitosis

    • Somatic cells

    • One cell division

    • Creates two identical diploid daughter cells

    • No crossing over/recombination

  • Meiosis

    • Gametes

    • Two cell divisions

    • Creates four genetically different daughter cells

    • Crossing over occurs in prophase I

    • Homologous pairs are separated in the first anaphase and chromatids are separated in the second anaphase

Products of meiosis in animals vs. plants, fungi, and algae

  • Animals

    • Meiosis makes haploid gametes, which fuse together at fertilization and grow into diploid organisms through mitosis

  • Plants

    • Diploid sporophytes make haploid spores using meiosis

    • Spores divide by mitosis to create gametophytes, which make gametes by mitosis

    • Gametes fuse together at fertilization to make a diploid zygote, which undergoes mitosis to return to the sporophyte stage

  • Fungi and algae

    • Diploid zygotes create haploid spores by meiosis

    • Spores divide by mitosis to make a gametophyte, which makes gametes by mitosis

    • Gametes fuse together at fertilization to return to a diploid zygote

Characteristics of homologous chromosomes

  • Carry the same genes

  • Centromeres are in the same place

  • Carry the same genes in the same place

  • Different distribution of SNP's and different types of alleles

  • Inherited from different parents

Mechanism by which recombination creates new combinations of alleles

  • Recombination occurs when homologous pairs line up one on top of the other and switch out pieces of their chromosomes at a chiasmata

  • Cutting all four backbones and pasting them to the other chromosome

Various mechanisms by which meiosis generates variation

Page 4:

  • Recombination:

    • Crossing over of the tetrads at the chiasmata creates new combinations of alleles during Prophase I.

  • Random Segregation:

    • Homologous pairs separate at Anaphase I, creating random combinations of maternal and paternal alleles.

    • Sister chromatids also separate randomly during Anaphase II.

  • Random joining of male and female gametes.

  • Segregation of various alleles during meiosis in monohybrid, dihybrid, and sex-linked situations.

  • Random Segregation:

    • Alleles segregate randomly into different haploid gametes.

  • Independent Assortment:

    • Applies to dihybrid crosses.

    • Different traits combine with each other randomly to produce combinations.

  • Sex-linked traits:

    • Linked to the X or Y chromosome.

    • Distributed differently based on offspring sex.

    • Males who inherit one X with the trait are called homozygous and express the trait.

    • Females must inherit two recessive or one dominant allele on an X to express the trait.

  • Other non-Mendelian inheritance patterns:

    • Incomplete dominance, Codominance, Epistasis, Polygenic inheritance, Pleiotropy, inactivation of one X chromosome, etc.

  • Conditions under which allele frequencies in a population will not change.

  • If a population is in Hardy-Weinberg equilibrium:

    • Allele frequencies in a population will not change.

  • Heterozygous advantage:

    • Allele frequencies have already leveled out.

  • Assortative mating:

    • Allele frequencies have already leveled out.

  • Hardy-Weinberg equilibrium assumptions:

    • No mutations occurring.

    • Population is closed to migration.

    • Infinite population size.

    • All genotypes are equally fit.

    • Random mating for the trait being considered.

  • How the dominance status of alleles affects their response to selection.

  • Selection against dominance:

    • Dominant allele disappears entirely.

  • Selection against recessive:

    • Recessive allele decreases in frequency but never completely disappears.

    • It stays hidden in the heterozygotes.

  • Heterozygote advantage:

    • Allele frequencies stabilize at 0.5, maintaining both alleles in the population.

    • Rare alleles will increase in frequency until they are no longer rare.

  • Homozygote advantage:

    • Rare alleles completely disappear.

    • Common allele goes to fixation.

    • Rare alleles are found mostly in heterozygotes, whereas common alleles are found mostly in homozygotes.

  • Relationship between selection and evolution.

  • Selection without evolution:

    • Occurs in heterozygote advantage after allele frequencies level out.

  • Evolution without selection:

    • Attributed to genetic drift and random mutations.

  • Calculate relative fitness from absolute fitness:

    • Absolute fitness is the average number of surviving offspring.

    • Relative fitness is calculated by dividing the absolute fitness of the genotype in question by the absolute fitness of the most successful genotype.

    • Relative fitness should be between 0 and 1.

  • How different types of selection and other evolutionary processes affect levels of heritable variation in a population.

  • Increases variation:

    • Gene flow, mutations.

  • Decreases variation:

    • Heterozygote disadvantage, genetic drift, selection against dominant and recessive alleles, assortative mating.

  • Maintains variation:

    • Heterozygote advantage, disassortative mating.

  • Whether or not a population is at genetic equilibrium (Hardy-Weinberg equilibrium), given observed genotype frequencies.

  • Calculate allele frequencies:

    • (# of homozygotes x 2 + # of heterozygotes) / number of organisms x 2.

    • The other allele frequency is 1 minus the calculated allele frequencies.

    • Plug the calculated allele frequencies into p^2, 2pq, and q^2.

    • If they create the same ratio of offspring, the population is in equilibrium.

  • Which assumptions of Hardy-Weinberg equilibrium have likely been violated, given an observed set of genotype or phenotype frequencies.

  • If lots of homozygotes, there was likely assortative mating.

  • Costs and benefits of reproducing sexually as opposed to asexually.

  • Cost of sexually reproducing:

    • Need to find a mate (could be dangerous).

    • Intrasexual selection causes males to decrease their survival fitness.

    • Males waste energy on sexual dimorphic traits.

    • Only pass on 0.5 of your alleles.

  • Cost of asexually reproducing:

    • More at risk for extinction.

    • Don't get the short-term benefits of sexual reproduction (genetic variability).

    • Fall behind in evolutionary arms race.

  • Why males usually compete for access to females (rather than vice versa), and why in some species this pattern is reversed.

  • Who is choosy and who competes depends on parental investment and potential fitness.

  • In most species, females have higher parental investment and lower potential fitness than males.

  • Females increase their potential fitness through quality offspring, while males increase their fitness through quantity of offspring.

  • Kin selection theory explains the persistence of helpful behavior.

  • Kin selection theory:

    • We help others that are related to us.

    • Our alleles continue to be passed on and our inclusive fitness increases.

  • Situations in which kin selection does or does not favor helping non-descendant relatives.

  • According to Hamilton's rule, kin selection favors helping non-descendant relatives when their relatedness to you multiplied by the benefit to them is greater than the cost to you (rb > c).

  • How asymmetries in relatedness can generate conflict between relatives.

  • Differences in opinion arise on when you should offer help based on the relatedness of other family members to the person in need.

  • Conditions that favor or disfavor cooperation between non-relatives.

  • Repeat interactions and the ability to recognize individuals who cooperate or cheated in the past favor cooperation.

  • One-time interactions or knowing the number of interactions favor selfishness.

  • Most recent common ancestor (MRCA) for a given group(s), given a phylogenetic tree.

  • The closest branching point shared between two groups is the MRCA.

  • Why some traditional groupings of organisms do not reflect evolutionary relationships.

  • Traditional groupings were made using morphological similarities without considering evolutionary history.

  • Relatively close and relatively distant relatives, given a phylogenetic tree.

  • Relatedness on a phylogenetic tree is determined by looking at the most recent common ancestor.

  • Monophyletic and non-monophyletic groupings in phylogenetic trees

    • Monophyletic groups (clades) include the MRCA and all descendants

    • Non-monophyletic groups include species from different lineages (polyphyletic) or include the ancestor but not all descendants (paraphyletic)

  • Parsimony in phylogenetic trees

    • The most parsimonious phylogeny has the least number of evolutionary changes

    • Considered correct until falsified

  • Distinction between homology and homoplasy

    • Homology: similarities due to common ancestry

    • Homoplasy: misleading similarity or dissimilarity due to convergent or divergent evolution

  • Determining the most likely phylogenetic tree

    • Look for synapomorphies (derived and shared traits)

    • Order species based on similarities to the out-group and to each other

  • Criteria used by different species concepts to define species

    • Morphological: based on physical appearance

    • Biological: based on ability to interbreed and produce fertile offspring

    • Phylogenetic: based on shared derived characteristics and evolutionary trees

  • Weaknesses/limitations of different species concepts

    • Morphological: not reliable alone, variation within species and convergent evolution

    • Biological: not applicable to asexual or extinct organisms, geographic separation

    • Phylogenetic: limited by unknown evolutionary history, may rely on morphological features

  • Species concept used in 'real world' examples

    • Morphological species concept used in field guides and for fossilized species

  • Why improving equipment for survival does not always lead to winning an evolutionary arms race

    • As one species evolves, the other species evolves in response

    • Improvement is necessary for survival, but not necessarily for surpassing the other species

  • Costs and benefits of being highly virulent for parasites

    • Cost: host dies sooner, unfavorable for transmission in low population density or direct contact

    • Benefit: quicker reproduction using host machinery, enhanced transmission in dense populations or indirect contact

  • How trade-offs, rapid environmental change, and arms races affect human susceptibility to disease

    • Arms race with parasites: parasites evolve quickly due to large population size and short generation times

    • Rapid environmental change: diseases of civilization, decrease in infectious diseases but increase in autoimmune disorders

    • Antagonistic pleiotropy: trade-offs between different aspects of fitness, harmful alleles kept through heterozygous advantage

  • Examples of proximate and ultimate explanations

    • Proximate explanation: physical and biochemical mechanisms underlying a trait

    • Ultimate explanation: role of natural selection, arms races, history, and chance in creating or continuing a trait

  • Costs and possible advantages of large brains

    • Cost: 2% of mass, 20% of energy

    • Possible advantages: utility hypothesis (survival-related skills) favored by natural selection, mating mind hypothesis (mating-related skills) favored by sexual selection

Skill Development Outcomes:

  1. Deep Learning

  • Making connections, understanding, and applying knowledge

  • Excludes memorization

  1. Serial Dilutions

  • Calculation of CFU/mL using dilution factor and volume of culture plate

  • Dilution factor calculated by dividing final volume by sample volume and multiplying by the denominator of serial dilution fractions

  1. Role of cyclin in the cell cycle

  • Cyclin regulates the rate of cell division and is important in cell cycle checkpoints

  1. Microscope calibration

  • Formula for measuring objects using stage divisions and ocular divisions

  • Calculation of magnification using ocular lens and objective lens

  1. Chi squared statistical analysis

  • Null Hypothesis and Alternate Hypothesis

    • Null Hypothesis states no effect/correlation/will be no change

    • Alternate Hypothesis states there is an effect/correlation/will be a change

  • Chi squared analysis

    • Determines if data is significant enough to support the alternate hypothesis

    • Compares observed values (collected in the study) with expected values (calculated based on null hypothesis)

    • Calculation: x^2 = sum of ((O-E)^2/E)

  • Degrees of freedom and critical value

    • Critical value is compared to chi-square value for statistical significance

    • Can be found on a chart or provided

  • Primary vs secondary scientific articles

    • Primary articles: original data and ideas from scientific investigations reported by scientists

    • Published in journals and contain sections like Abstract, Introduction, Methods, Results, Discussion, References

    • Secondary articles: review and analyze primary sources in more depth

  • FST Population Genetics

    • FST = 1 - (average heterozygosity expected within populations / heterozygosity expected across total population)

    • HS = (2p1q1 + 2p2q2)/2

    • HT = 2pTqT

    • Use Hardy-Weinberg to calculate p and q values for individual populations, then add population numbers together and recalculate for the total

    • Interpretation of FST values:

      • FST = 0: no disturbance

      • FST > 0.25: significant disturbance

      • FST = 1: complete separation of populations

  • Allozyme Electrophoresis for genetic variability calculation

    • Takes advantage of the fact that organisms produce allelic variants of enzymes called allozymes

    • Each allozyme has a slightly different amino acid sequence and is the product of a unique allele

    • Genotype at a gene locus coding for an enzyme can be inferred from the number and position of spots observed on gels

    • Genetic variation in a population is the average frequency of heterozygous individuals per locus

    • Calculated by determining the frequency of heterozygotes at each locus and averaging these frequencies over all loci

  • Creating phylogenetic trees using DNA sequencing

    • Phylogenies can be estimated by looking at differences in DNA sequence

    • Species with the most differences is the out-group

    • If no differences, it is the same species and should be drawn on the same vertical line

    • Length of horizontal lines may indicate the

Biology Essential Outcomes

Biology 1001: Essential Outcomes

Principles underlying evolution by natural selection

  • Mutations arise in a population randomly

    • Recombination in sexual reproduction during meiosis (crossing over)

  • If a mutation is favorable, the organism will survive and reproduce to pass on the allele

  • Over time, the frequency of this allele will rise in the population = evolution

Evidence supporting descent with modification from a common ancestor

  • Historical Biogeography

    • Studies of the world distribution of plants and animals

  • Comparative Morphology

    • Comparing anatomical structures of organisms (vestigial structures) and embryonic development similarities

  • Geology

    • Looking at fossils representing organisms

Characteristics of a scientific theory and the importance of falsifiability

  • Theories are testable hypotheses about the natural world

  • Must be falsifiable to be considered scientific

  • Must be objective, not mythical, cannot be a definition, can't be faith-based, and must be reasonably possible to test

Changes in amount of DNA throughout the cell cycle

  • G1: One copy of DNA

  • S: DNA is copied

  • G2: Two copies of DNA

  • M: prophase-metaphase (n=2, c=4) anaphase-telophase (n=2, c=2)

Main features of each stage of mitosis with respect to the cytoskeleton and the chromatin

  • Prophase

    • Chromatin condenses, nucleolus disappears, spindle (microtubules) begin forming and moving to poles, nuclear membrane breaks down

  • Pro-metaphase

    • Microtubules grow from centrosomes towards cell center, spindles attach to chromosome kinetochores

  • Metaphase

    • Spindle microtubules move chromosomes into alignment, chromosomes complete condensation

  • Anaphase

    • Sister chromatids separate and move along spindles using kinetochore motor, some spindles push each other and some pull chromosomes

  • Telophase

    • Spindle disassembles, nucleolus and nuclear envelope reappear

Cytokinesis

  • Cleavage furrow

    • Layer of microtubules stretches across spindle midpoint

    • A band of microfilaments (actin) forms in plasma membrane and tightens to squeeze off cell into two

  • Cell Plate

    • Layer of microtubules in the middle is covered in vesicles across the entire cell

    • Vesicles fuse together to make a new cell wall splitting the cell in half

Structure of a replication bubble

  • Origin of replication is in the middle

  • Replication fork unzips from this point in opposite directions

  • Leading strand (one RNA primer extended) and lagging strand (multiple RNA primers added in Okazaki fragments) for each side of the bubble

  • Linear chromosomes have many simultaneous bubbles, circular chromosomes have only one at a time

Relationship between DNA replication and metaphase chromosome structure

  • DNA has been replicated in Interphase and stays together as two sister chromatids up until Metaphase

  • Each chromosome in Metaphase contains two double helixes (extremely condensed and attached at a centromere)

Difference between DNA damage and mutation

  • Damage is a single-stranded change in the DNA

  • Mutations are any double-stranded change in the DNA sequence

  • Mutations may arise from initial damage and can be good or bad, but are necessary for evolution

Origin of various types of genomic variation

  • SNP's (Single Nucleotide Polymorphisms)

    • Caused by replication errors and tautomeric shifts

  • CNV's (Copy Number Variations)

    • Caused by uneven crossing over

  • In/Del

    • Caused by "slippage" when many of the same nitrogen base are next to each other in a sequence

  • Duplication, Inversion, Translocation, and Large Deletions

    • May occur due to ionizing radiation that creates reactive O2 that steal electrons and break chromosomes

    • Non-homologous end joining pastes the end back together and is highly mutagenic

  • Mobile elements

    • Insertion sequences, transposons, retrotransposons, and retroviruses exist and move throughout the genome

    • Cut and paste or copy and paste mechanisms without the enzyme transposase

    • Increase genetic variability

Main differences between meiosis and mitosis

  • Mitosis

    • Somatic cells

    • One cell division

    • Creates two identical diploid daughter cells

    • No crossing over/recombination

  • Meiosis

    • Gametes

    • Two cell divisions

    • Creates four genetically different daughter cells

    • Crossing over occurs in prophase I

    • Homologous pairs are separated in the first anaphase and chromatids are separated in the second anaphase

Products of meiosis in animals vs. plants, fungi, and algae

  • Animals

    • Meiosis makes haploid gametes, which fuse together at fertilization and grow into diploid organisms through mitosis

  • Plants

    • Diploid sporophytes make haploid spores using meiosis

    • Spores divide by mitosis to create gametophytes, which make gametes by mitosis

    • Gametes fuse together at fertilization to make a diploid zygote, which undergoes mitosis to return to the sporophyte stage

  • Fungi and algae

    • Diploid zygotes create haploid spores by meiosis

    • Spores divide by mitosis to make a gametophyte, which makes gametes by mitosis

    • Gametes fuse together at fertilization to return to a diploid zygote

Characteristics of homologous chromosomes

  • Carry the same genes

  • Centromeres are in the same place

  • Carry the same genes in the same place

  • Different distribution of SNP's and different types of alleles

  • Inherited from different parents

Mechanism by which recombination creates new combinations of alleles

  • Recombination occurs when homologous pairs line up one on top of the other and switch out pieces of their chromosomes at a chiasmata

  • Cutting all four backbones and pasting them to the other chromosome

Various mechanisms by which meiosis generates variation

Page 4:

  • Recombination:

    • Crossing over of the tetrads at the chiasmata creates new combinations of alleles during Prophase I.

  • Random Segregation:

    • Homologous pairs separate at Anaphase I, creating random combinations of maternal and paternal alleles.

    • Sister chromatids also separate randomly during Anaphase II.

  • Random joining of male and female gametes.

  • Segregation of various alleles during meiosis in monohybrid, dihybrid, and sex-linked situations.

  • Random Segregation:

    • Alleles segregate randomly into different haploid gametes.

  • Independent Assortment:

    • Applies to dihybrid crosses.

    • Different traits combine with each other randomly to produce combinations.

  • Sex-linked traits:

    • Linked to the X or Y chromosome.

    • Distributed differently based on offspring sex.

    • Males who inherit one X with the trait are called homozygous and express the trait.

    • Females must inherit two recessive or one dominant allele on an X to express the trait.

  • Other non-Mendelian inheritance patterns:

    • Incomplete dominance, Codominance, Epistasis, Polygenic inheritance, Pleiotropy, inactivation of one X chromosome, etc.

  • Conditions under which allele frequencies in a population will not change.

  • If a population is in Hardy-Weinberg equilibrium:

    • Allele frequencies in a population will not change.

  • Heterozygous advantage:

    • Allele frequencies have already leveled out.

  • Assortative mating:

    • Allele frequencies have already leveled out.

  • Hardy-Weinberg equilibrium assumptions:

    • No mutations occurring.

    • Population is closed to migration.

    • Infinite population size.

    • All genotypes are equally fit.

    • Random mating for the trait being considered.

  • How the dominance status of alleles affects their response to selection.

  • Selection against dominance:

    • Dominant allele disappears entirely.

  • Selection against recessive:

    • Recessive allele decreases in frequency but never completely disappears.

    • It stays hidden in the heterozygotes.

  • Heterozygote advantage:

    • Allele frequencies stabilize at 0.5, maintaining both alleles in the population.

    • Rare alleles will increase in frequency until they are no longer rare.

  • Homozygote advantage:

    • Rare alleles completely disappear.

    • Common allele goes to fixation.

    • Rare alleles are found mostly in heterozygotes, whereas common alleles are found mostly in homozygotes.

  • Relationship between selection and evolution.

  • Selection without evolution:

    • Occurs in heterozygote advantage after allele frequencies level out.

  • Evolution without selection:

    • Attributed to genetic drift and random mutations.

  • Calculate relative fitness from absolute fitness:

    • Absolute fitness is the average number of surviving offspring.

    • Relative fitness is calculated by dividing the absolute fitness of the genotype in question by the absolute fitness of the most successful genotype.

    • Relative fitness should be between 0 and 1.

  • How different types of selection and other evolutionary processes affect levels of heritable variation in a population.

  • Increases variation:

    • Gene flow, mutations.

  • Decreases variation:

    • Heterozygote disadvantage, genetic drift, selection against dominant and recessive alleles, assortative mating.

  • Maintains variation:

    • Heterozygote advantage, disassortative mating.

  • Whether or not a population is at genetic equilibrium (Hardy-Weinberg equilibrium), given observed genotype frequencies.

  • Calculate allele frequencies:

    • (# of homozygotes x 2 + # of heterozygotes) / number of organisms x 2.

    • The other allele frequency is 1 minus the calculated allele frequencies.

    • Plug the calculated allele frequencies into p^2, 2pq, and q^2.

    • If they create the same ratio of offspring, the population is in equilibrium.

  • Which assumptions of Hardy-Weinberg equilibrium have likely been violated, given an observed set of genotype or phenotype frequencies.

  • If lots of homozygotes, there was likely assortative mating.

  • Costs and benefits of reproducing sexually as opposed to asexually.

  • Cost of sexually reproducing:

    • Need to find a mate (could be dangerous).

    • Intrasexual selection causes males to decrease their survival fitness.

    • Males waste energy on sexual dimorphic traits.

    • Only pass on 0.5 of your alleles.

  • Cost of asexually reproducing:

    • More at risk for extinction.

    • Don't get the short-term benefits of sexual reproduction (genetic variability).

    • Fall behind in evolutionary arms race.

  • Why males usually compete for access to females (rather than vice versa), and why in some species this pattern is reversed.

  • Who is choosy and who competes depends on parental investment and potential fitness.

  • In most species, females have higher parental investment and lower potential fitness than males.

  • Females increase their potential fitness through quality offspring, while males increase their fitness through quantity of offspring.

  • Kin selection theory explains the persistence of helpful behavior.

  • Kin selection theory:

    • We help others that are related to us.

    • Our alleles continue to be passed on and our inclusive fitness increases.

  • Situations in which kin selection does or does not favor helping non-descendant relatives.

  • According to Hamilton's rule, kin selection favors helping non-descendant relatives when their relatedness to you multiplied by the benefit to them is greater than the cost to you (rb > c).

  • How asymmetries in relatedness can generate conflict between relatives.

  • Differences in opinion arise on when you should offer help based on the relatedness of other family members to the person in need.

  • Conditions that favor or disfavor cooperation between non-relatives.

  • Repeat interactions and the ability to recognize individuals who cooperate or cheated in the past favor cooperation.

  • One-time interactions or knowing the number of interactions favor selfishness.

  • Most recent common ancestor (MRCA) for a given group(s), given a phylogenetic tree.

  • The closest branching point shared between two groups is the MRCA.

  • Why some traditional groupings of organisms do not reflect evolutionary relationships.

  • Traditional groupings were made using morphological similarities without considering evolutionary history.

  • Relatively close and relatively distant relatives, given a phylogenetic tree.

  • Relatedness on a phylogenetic tree is determined by looking at the most recent common ancestor.

  • Monophyletic and non-monophyletic groupings in phylogenetic trees

    • Monophyletic groups (clades) include the MRCA and all descendants

    • Non-monophyletic groups include species from different lineages (polyphyletic) or include the ancestor but not all descendants (paraphyletic)

  • Parsimony in phylogenetic trees

    • The most parsimonious phylogeny has the least number of evolutionary changes

    • Considered correct until falsified

  • Distinction between homology and homoplasy

    • Homology: similarities due to common ancestry

    • Homoplasy: misleading similarity or dissimilarity due to convergent or divergent evolution

  • Determining the most likely phylogenetic tree

    • Look for synapomorphies (derived and shared traits)

    • Order species based on similarities to the out-group and to each other

  • Criteria used by different species concepts to define species

    • Morphological: based on physical appearance

    • Biological: based on ability to interbreed and produce fertile offspring

    • Phylogenetic: based on shared derived characteristics and evolutionary trees

  • Weaknesses/limitations of different species concepts

    • Morphological: not reliable alone, variation within species and convergent evolution

    • Biological: not applicable to asexual or extinct organisms, geographic separation

    • Phylogenetic: limited by unknown evolutionary history, may rely on morphological features

  • Species concept used in 'real world' examples

    • Morphological species concept used in field guides and for fossilized species

  • Why improving equipment for survival does not always lead to winning an evolutionary arms race

    • As one species evolves, the other species evolves in response

    • Improvement is necessary for survival, but not necessarily for surpassing the other species

  • Costs and benefits of being highly virulent for parasites

    • Cost: host dies sooner, unfavorable for transmission in low population density or direct contact

    • Benefit: quicker reproduction using host machinery, enhanced transmission in dense populations or indirect contact

  • How trade-offs, rapid environmental change, and arms races affect human susceptibility to disease

    • Arms race with parasites: parasites evolve quickly due to large population size and short generation times

    • Rapid environmental change: diseases of civilization, decrease in infectious diseases but increase in autoimmune disorders

    • Antagonistic pleiotropy: trade-offs between different aspects of fitness, harmful alleles kept through heterozygous advantage

  • Examples of proximate and ultimate explanations

    • Proximate explanation: physical and biochemical mechanisms underlying a trait

    • Ultimate explanation: role of natural selection, arms races, history, and chance in creating or continuing a trait

  • Costs and possible advantages of large brains

    • Cost: 2% of mass, 20% of energy

    • Possible advantages: utility hypothesis (survival-related skills) favored by natural selection, mating mind hypothesis (mating-related skills) favored by sexual selection

Skill Development Outcomes:

  1. Deep Learning

  • Making connections, understanding, and applying knowledge

  • Excludes memorization

  1. Serial Dilutions

  • Calculation of CFU/mL using dilution factor and volume of culture plate

  • Dilution factor calculated by dividing final volume by sample volume and multiplying by the denominator of serial dilution fractions

  1. Role of cyclin in the cell cycle

  • Cyclin regulates the rate of cell division and is important in cell cycle checkpoints

  1. Microscope calibration

  • Formula for measuring objects using stage divisions and ocular divisions

  • Calculation of magnification using ocular lens and objective lens

  1. Chi squared statistical analysis

  • Null Hypothesis and Alternate Hypothesis

    • Null Hypothesis states no effect/correlation/will be no change

    • Alternate Hypothesis states there is an effect/correlation/will be a change

  • Chi squared analysis

    • Determines if data is significant enough to support the alternate hypothesis

    • Compares observed values (collected in the study) with expected values (calculated based on null hypothesis)

    • Calculation: x^2 = sum of ((O-E)^2/E)

  • Degrees of freedom and critical value

    • Critical value is compared to chi-square value for statistical significance

    • Can be found on a chart or provided

  • Primary vs secondary scientific articles

    • Primary articles: original data and ideas from scientific investigations reported by scientists

    • Published in journals and contain sections like Abstract, Introduction, Methods, Results, Discussion, References

    • Secondary articles: review and analyze primary sources in more depth

  • FST Population Genetics

    • FST = 1 - (average heterozygosity expected within populations / heterozygosity expected across total population)

    • HS = (2p1q1 + 2p2q2)/2

    • HT = 2pTqT

    • Use Hardy-Weinberg to calculate p and q values for individual populations, then add population numbers together and recalculate for the total

    • Interpretation of FST values:

      • FST = 0: no disturbance

      • FST > 0.25: significant disturbance

      • FST = 1: complete separation of populations

  • Allozyme Electrophoresis for genetic variability calculation

    • Takes advantage of the fact that organisms produce allelic variants of enzymes called allozymes

    • Each allozyme has a slightly different amino acid sequence and is the product of a unique allele

    • Genotype at a gene locus coding for an enzyme can be inferred from the number and position of spots observed on gels

    • Genetic variation in a population is the average frequency of heterozygous individuals per locus

    • Calculated by determining the frequency of heterozygotes at each locus and averaging these frequencies over all loci

  • Creating phylogenetic trees using DNA sequencing

    • Phylogenies can be estimated by looking at differences in DNA sequence

    • Species with the most differences is the out-group

    • If no differences, it is the same species and should be drawn on the same vertical line

    • Length of horizontal lines may indicate the