AP BIO HEREDITY VOCAB

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57 Terms

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heredity
the transmission of traits from one generation to the next
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genes
segments of DNA that code for basic units of hereditary
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mutations
a random error in gene replication that leads to a change
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homologous chromosomes
Pair of chromosomes that are the same size, same appearance and same genes.
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asexual reproduction
Process by which a single parent reproduces by itself
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sexual reproduction
A reproductive process that involves two parents that combine their genetic material to produce a new organism, which differs from both parents
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karyotype
A display of the chromosome pairs of a cell arranged by size and shape.
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somatic cells
body cells
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gamete cells
sex cells
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diploid 2n
two copies of each chromosome
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haploid n
An organism or cell having only one complete set of chromosomes.
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autosome
Any chromosome that is not a sex chromosome
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sex chromosome
Chromosomes that determine the sex of an individual
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life cycle
The generation-to-generation sequence of stages in the reproductive history of an organism.
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zygote
fertilized egg
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genetics
The scientific study of heredity
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clones
identical genetic copies
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meiosis
Cell division that produces reproductive cells in sexually reproducing organisms
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synapsis
Pairing of homologous chromosomes
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tetrad
structure containing 4 chromatids that forms during meiosis
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chiasmata
X-shaped regions where crossing over occurred.
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crossing over
Process in which homologous chromosomes exchange portions of their chromatids during meiosis.
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independent assortment
One of Mendel's principles that states that genes for different traits can segregate independently during the formation of gametes
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steps of meiosis
Prophase 1, Metaphase 1, Anaphase 1, Telophase 1, Prophase 2, Metaphase 2, Anaphase 2, Telophase 2
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true breeding
term used to describe organisms that produce offspring identical to themselves if allowed to self-pollinate
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p generation
Parental generation, the first two individuals that mate in a genetic cross
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f1 generation, first filial generation
offspring of the P generation
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f2 generation. 2nd filial generation
offspring of the F1 generation
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punnet squares
diagram showing the gene combinations that might result from a genetic cross
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monohybrid cross
A cross between individuals that involves one pair of contrasting traits
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dihybrid cross
A cross between individuals that have different alleles for the same gene
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phenotype
An organism's physical appearance, or visible traits.
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the multiplication rule
To determine the probability, we multiply the probability of one event by the probability of another.
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law of segregation
Mendel's law that states that the pairs of homologous chromosomes separate in meiosis so that only one chromosome from each pair is present in each gamete
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law of independent assortment
the law that states that genes separate independently of one another in meiosis
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the addition rule
Considering mutually exclusive events, the probability of both occurring is the sum of the probabilities of each event.
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recessive
An allele that is masked when a dominant allele is present
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alleles
Different forms of a gene
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heterozygous
An organism that has two different alleles for a trait
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genotype
genetic makeup of an organism
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dominant
Describes a trait that covers over, or dominates, another form of that trait.
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homozygous
An organism that has two identical alleles for a trait
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pedigrees
a chart that shows a trait in a family and how it is inherited
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incomplete dominance
Situation in which one allele is not completely dominant over another allele
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polygenic inheritance
combined effect of two or more genes on a single character
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multiple alleles
three or more forms of a gene that code for a single trait
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epistasis
A type of gene interaction in which one gene alters the phenotypic effects of another gene that is independently inherited.
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x linked
referring to a gene located on the X chromosome
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codominance
A condition in which neither of two alleles of a gene is dominant or recessive.
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y linked
referring to a gene located on the Y chromosome
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hemizygous
A gene present on the X chromosome that is expressed in males in both the recessive and dominant condition
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barr body
A dense body formed from a deactivated X chromosome.
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recombinants
offspring whose phenotype differs from that of the parents
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linkage map
A genetic map based on the frequencies of recombination between markers during crossing over of homologous chromosomes.
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chi square
Involves categorical variables. Looks at 2 distributions of categorical data to see if they differ from each other.
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phenotypic plasticity
the ability of one genotype to produce more than one phenotype when exposed to different environments
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nondisjunction
Error in meiosis in which homologous chromosomes fail to separate.