Biology Essential Outcomes
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
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
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
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)
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
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
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
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)
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
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
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
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
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
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
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
Deep Learning
Making connections, understanding, and applying knowledge
Excludes memorization
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
Role of cyclin in the cell cycle
Cyclin regulates the rate of cell division and is important in cell cycle checkpoints
Microscope calibration
Formula for measuring objects using stage divisions and ocular divisions
Calculation of magnification using ocular lens and objective lens
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
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
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
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
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)
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
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
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
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)
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
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
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
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
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
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
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
Deep Learning
Making connections, understanding, and applying knowledge
Excludes memorization
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
Role of cyclin in the cell cycle
Cyclin regulates the rate of cell division and is important in cell cycle checkpoints
Microscope calibration
Formula for measuring objects using stage divisions and ocular divisions
Calculation of magnification using ocular lens and objective lens
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