Bio - EOYT.

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44 Terms

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Mitosis

A form of cell division resulting in two daughter cells from a mother cell - identical

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Chromosomes

Condensed forms of DNA located in the nucleus of a cell

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Chromatid

One half of a chromosome

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Centromere

The region of a chromosome where the two sister chromatids are joined and where spindle fibers attach during cell division.

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  • spindle

  • cell pole

  • equator

  • Come from centrioles (used to separate chromatids)

  • opposite sides of a cell

  • the mid plain of a cell

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Homologous chromosomes

Chromosome pairs, one from each parent, that are similar in shape, size, and genetic content.

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Meiosis

A type of cell division that reduces the chromosome number by half, resulting in four genetically diverse gametes, crucial for sexual reproduction. - except for 3 polar bodies in oogenesis

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Diploid vs haploid

  • double vs half (full chromosome set vs half set)

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Cell cycle - interphase

  • G1 phase - initial growth phase + copying of organelles

  • S phase - DNA duplication phase - centrosomes duplicated

  • G2 phase - further growth

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Prophase - mitosis

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Prophase - meiosis

knowt flashcard image
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Metaphase

  • chromosomes align at the equator (homologous if meiosis)

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Anaphase

Chromosomes or chromatids pulled apart by spindle fibers from centrioles (in the centrosomes)

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Telophase

knowt flashcard image
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Variation

  • Crossing over

  • Random arrangement

  • Random assortment

  • Non-disjunction/other mutations

  • Fertilization

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Gene

Small segment of DNA that codes for a specific trait

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Alleles

Alternate forms of one trait (brown hair and ginger hair)

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Homozygous

Two of the same characteristics

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Heterozygous

Two different alleles for one trait

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Genotype

The gene composition of an individual

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Phenotype

Physically visible characteristics of a certain genotype

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Law of segregation

When gametes form, alleles are separated so that each gamete carries only one allele for each gene

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Law of independent assortment

The segregation of alleles for one gene occurs independently to that of any other gene

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Law of dominance

Recessive alleles will be masked by dominant alleles

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Autosomal traits

Traits that are located on any chromosome except for the sex chromosomes

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Both parents affected, child unaffected

Dominant trait, heterozygous parents

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All affected individuals…

..must have an affected parent - dominant trait

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Both parents are unaffected, then children also unaffected

Parents would be homozygous recessive and trait dominant

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If both parents are unaffected and child is affected..

Trait must be recessive (parents are heterozygous carriers)

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If both parents show trait, child must too

Homozygous recessive for trait

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Co-dominance

Both genotypes are dominant and are equally represented in the phenotype

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Incomplete dominance

Both genes mix together to create a new and unique phenotype

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Sex-linked traits

Sex linkage refers to when a gene controlling a characteristic is located on a sex chromosome (X or Y)

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Rule 1:

Only females can be carriers (a heterozygote for a recessive disease condition), males cannot be heterozygous carriers (they have only 1 X-chromosome)

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Rule 2:

Males will always inherit an X-linked trait from their mother (they inherit a Y chromosome from their father)

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Rule 3:

Females cannot inherit an X-linked recessive condition from an unaffected father (must receive his dominant allele)

  • so he is unaffected and therefore doesn’t have the recessive gene, so daughter wouldn’t inherit it from him but perhaps would from mother

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Unlinked genes

Gene loci on different chromosomes and are independent of one another

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Di-hybrid cross

Determines the genotypic and phenotypic rations of two unlinked traits (so hair colour and eye colour)

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Discontinuous variation

  • Organism either has it or not

  • Qualitative

  • Only determined by genes

  • eg. blood type or sex

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Continuous variation

  • determined by genes and environmental influence

  • every organism shows gene but to different extent

  • several genes acting together

  • quantitative

  • use di-hybrid cross to express

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Causes of mutation

  • Mistake in copying DNA

  • DNA damage

  • eg. radiation, chemicals, etc.

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Adaption

An organism that is well –suited to make the most out of the limited resources within its environment is said to show adaptation

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Process of evolution

  • Over production/genetic variation

  • Struggle for existence/environmental pressure

  • Variation/adaption

  • Natural selection/survival of the fittest

  • speciation

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Evidence of evolution

  • analysis of fossils - compare to existing creatures and create family tree

  • bio-geographical location - continental drift

  • comparative anatomy - homologous(same structure different function) + analogous (different structure, same function)

  • DNA (mitochondrial) - passed down from mother and can analyse tree line