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Work Cited Zhang, Michael. ““It’s Test Time Again” (Melanin Test).” Google Docs, Bergen County Academies, 25 Mar. 2026, docs.google.com/document/d/1SE7iX0RAkWfy7Ix1e9ZK_KP-x5kv8KGnkwKMufkDkPU/edit?tab=t.424l8898onwj#heading=h.ck5ezwhcvnm. Accessed 25 Mar. 2026.
DNA
deoxyribonucleic acid, is in the nucleus and contains genetic information in chromosomes
Gene
A segment of DNA on a chromosome that codes for a specific trait
Chromosome
a threadlike structure of DNA, containing genetic information
Incomplete Dominance
Both alleles are blended, resulting in offspring with a mix of their parents' traits (Ex: White flower + Red flower = Pink flower)
Codominance
Both alleles are expressed (Ex: Brown Cow + White Cow = Brown cow with some white)
Multiple Alleles
Multiple alleles coding for the same gene, each with varying levels of dominance (Ex: Black > Chinchilla > Himalayan > Albino fur colors in rabbits)
Dihybrid Crosses
4x4 punnet square, checks for two traits rather than 1
Polygenic inheritance
Multiple genes affect a single trait, usually resulting in a spectrum of traits rather than a set (Ex: Skin color)
Law of Independent Assortment
Mendel's law, states that allele pairs separate from one another during gamete formation
Epistasis
One gene masks another (Ex: In dog coats, the A allele can be affected if the dog contains the B allele)
Albinism Inheritance
Autosomal recessive trait that causes one from a dark skinned family to have light skin
Mutation
An error made when replicating a gene that changes the codon sequence, changing the amino acid sequence and the trait expressed
Insertion
The addition of nucleotides to a codon, causing the rest of the sequence to frameshift down (AGC GCA -> ACG CGC)
Deletion
The removal of nucleotides in a codon, causing the rest of the sequence to frameshift up (AGC GCA -> ACG CAG)
Substitution
The replacement of a single codon (AGC GCA -> GCA GCA)
Frameshift
Inserting or deleting nucleotides (not a multiple of 3) that cause the reading frame of the sequence to shift
Missense
One singular base is swapped for another, resulting in a different amino acid
Nonsense
A genetic mutation resulting in a stop codon, ending the amino acid sequence early
Silent
A genetic mutation that changes a codon but does not alter the amino acid sequence
Transcription
The process occurring in the nucleus where RNA polymerase copies a DNA sequence into mRNA with a complementary sequence, replacing thymine with uracil
Translation
mRNA is released into the cytoplasm and reaches the ribosome (rRNA). tRNA with complementary codons then match with each codon, and each codon maps to a specific amino acid.
mRNA
messenger RNA; carries instructions for amino acid structure
rRNA
ribosomal RNA; catalyzes the forming of peptide bonds between amino acids
tRNA
transfer RNA; brings the amino acid correlating to the codon on the mRNA, matches based on its complementary anticodon
Cell Nucleus
The location of DNA
Codon
Bases on mRNA grouped in threes
Anticodon
Found on tRNA, is complementary to the codon
Amino Acid
Monomer of protein
Protein Synthesis
the formation of proteins by using information contained in DNA and carried by mRNA (transcription + translation)
Protein Shape
Determined by the amino acid sequence, results in different traits
Protein Function
Structure, enzymes, cell signaling
Melanin
A pigment that gives the skin its color
Pheomelanin
Melanin that causes lighter skin color. Is more common further from the equator
Eumelanin
Melanin that causes darker skin color. Is more common closer to the equator
Effect of UV Radiation
UVB required for the body to synthesize Vitamin D, UV rays destroy folate
Vitamin D
Deficiencies of vitamin D can cause rickets and other bone diseases
Folate
Prevents certain events that can harm pregnancy
Consequences of Light Skin close to the Equator
Folate destroyed
Consequences of Dark Skin far from the Equator
Little vitamin D is synthesized
Selective Advantage
A trait within an organism that gives it a higher chance of reproduction
Selective Pressure
The environment pushing against or towards the passing down of specific traits
Fitness
Ability of an organism to survive and reproduce in its environment
Pedigree
A chart or "family tree" that tracks which members of a family have a particular trait
Karyotype
The complete set of chromosomes within an individual
Punnet Square
A chart that shows all the possible combinations of alleles that can result from a genetic cross
Genotype
The genetic makeup of an organism (Ex: Bb)
Phenotype
An observable trait of an organism (Ex: Red in color)
Stabilizing Selection
Selects for average traits (Ex: Robins lay four eggs because too little eggs result in little offspring and too many eggs result in malnourishment)
Directional Selection
Selects for an extreme trait (Ex: Dark mice develop on dark rock pockets because light mice are more easily caught by predators)
Diversifying Selection
Selects for traits away from the average one, occasionally causing different species (Ex: Gray and Himalayan rabbits are hard to spot, while white rabbits are easy to prey on)
Related Species
Have a recent common ancestor
Divergent Evolution
Related species adapt with different traits
Artificial Selection
Humans select traits they want to see in offspring, developing new species
Adaptive Radiation
A group of organisms quickly diverges into new species because of environmental stresses
Convergent Evolution
Unrelated species evolve to become more similar because they live in similar habitats
Analogous Structures
Found in convergent evolution; different structures with the same function
Gradualism
Continuous change at a constant pace (gradually)
Punctuated Equilibrium
Rapid bursts of evolution followed by long periods of stability (equilibrium)
Coevolution
A species evolves in response to another (Ex: As newts produce more toxins, snakes that consume them gain more resistance)
Allopatric Speciation
New species are formed when physically separated or occupying different geographical areas (often due to a change in environment)
Sympatric Speciation
New species are formed when occupying the same area and separated by reproductive or behavioral differences
Prezygotic Isolation
A barrier to breeding that occurs before fertilization
Postzygotic Isolation
A barrier to breeding that occurs after fertilization
Temporal Isolation
prezygotic barrier: two species mate at a different time of year
Ecological Isolation
prezygotic barrier: two species inhabit similar regions but occupy different habitats
Behavioral Isolation
prezygotic barrier: two species respond to different specific courtship patterns
Mechanical Isolation
prezygotic barrier: genital differences prevent two species from being physically capable of mating
Hybrid Inviability
postzygotic barrier: hybrids are produced but fail to develop to reproductive maturity
Hybrid Infertility
postzygotic barrier: hybrids fail to produce functional gametes
Hybrid Breakdown
F1 hybrids are fertile but the F2 generation either fails to develop or is infertile
Hardy Weinberg Equation
p + q = 1, p^2 +2pq + q^2 = 1
Frequency of allele
The total amount of instances of a specific allele in a population divided by the total amount of alleles in a population
Frequency of a genotype
The total amount of instances of a specific genotype in a population divided by the total amount of genotypes
p
Frequency of the dominant allele
q
Frequency of the recessive allele
p^2
Frequency of the homozygous dominant genotype
2pq
Frequency of the heterozygous genotype
q^2
Frequency of the homozygous recessive genotype
Product Rule
Used when the probability of two or more events happening simultaneously is being tracked (and), probability of each individual event is multiplied
Sum Rule
Used when the probability of two or more mutually exclusive events are being tracked (or), probability of each individual event is added
Gene Flow
Movement of alleles from one population to another
Genetic Drift
A random change in the allele frequency of a population
True Breeding
Organisms that produce offspring identical to themselves if allowed to self-pollinate (homozygous)
Hybrids
A cross between different varieties of organisms
P generation
The true-breeding parents
F1 generation
Hybrid offspring of the P generation
F2 generation
Offspring of the F1 generation
Law of Segregation
A gamete only contains one chromosome from each pair
Locus
Location of a gene on a chromosome
Testcross
The mating of an individual with an unknown genotype and an individual with a homozygous recessive genotype
Carriers
Heterozygous individuals who carry the recessive allele, but display the dominant trait
Type A Blood
AA or Ai: contains A antigens and anti-B antibodies, can receive A and O blood
Type B Blood
BB or Bi: contains B antigens and anti-A antibodies, can receive B and O blood
Type AB Blood
AB: contains A and B antigens and no antibodies, can receive any blood
Type O Blood
ii: contains no antigens and A and B antibodies, cannot receive any blood
What happens when an individual receives the wrong blood?
Antibodies attack the antigens and cause clotting
Autosomal Chromosomes
Non sex chromosomes, 22 pairs found in humans
Sex Chromosomes
XX codes for a female, XY codes for a male. Only 1 pair of sex chromosomes in a human
Sex-linked genes
Gene located on a sex chromosome. X linked recessive traits are more common in males because they only have one X chromosome, and the trait cannot be masked
Pleiotropy
A single gene influences multiple traits