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100 Cards in this Set

  • Front
  • Back
a comparison between populations of organisms in one area to another
biogeography
the time it takes one half of the mass of a radioactive element to decay
half-life
structures that have the same origin
homologous structures
structures that have the same function
analogous function
in the development of organisms there is a record of how that organism evolved according to Ernst Haekel
ontogeny recapitulates phylogeny
carbon 14
half life - 5600 yrs
limit - 50000 yrs
potassium 40
half life - 1.3 billion
limit - mega years
fish with lobes as fins
coelocanth
birds part dinosaur
archeoptryx
4 theory of Darwin and Wallace
variation exists in all population
overpopulation of offspring
survival of the fittest
differential reproduction and survival produces new species
mutation that can be mapped to a single locus
point mutation
selective elimination of phenotypes at both extremes
stabilizing selection
selective force that changes the frequency of alleles in a given direction
directional selection
selection towards both extremes against the average
disruptive selection
genetic drift from the reduction of alleles in a popultaion usually caused by a natural disaster
bottleneck effect
small, semi-isolated population that when it continues to grow diversifies from the population that it originally stemmed from
founder effect
reproductive isolation that occurs before a zygote is formed which keeps offspring from surviving or reproducing
postzygotic isolation
speciation driven by a geographic barrier
allopatric speciation
speciation driven be a reproductive barrier - prezygotic isolating mechanisms`
sympatric speciation
factors that reduce the possibility of interbreeding between geographically isolated populations that somehow come into contact
isolating mechanism
cell division in eukarytic cells consisting of various stages PMAT. used to produce 2 identical daughter cells
mitosis
region of chromosome that attaches to spindle fibers
centromere
an arbitrary number assigned to a molecule of DNA for keeping track of DNA quantitatively
units of DNA
stage during mitosis and meiosis in which the chromosomes line up along the center of the cell
metaphase
reduction division
cell division in sex cells consisting of 8 phases. used to produce 4 gametes each containing half the chromosomes number of parent cell
meiosis
exact copies of the same chromosome, complexed together at the centromere, separating during mitosis and meiosis
sister chromatids
haploid cell derived from meiosis in the ovaries containing very little cytoplasm compared to a mature ovum
polar bodies
stage during mitosis and meiosis 2 in which the sister chromatids are pulled apart. In meiosis 1, the tetrad pairs are separated.
anaphase
organism or cell consisting of one set of chromosomes. found in sex cells, sperm and egg.
haploid
process occurring in the female ovaries in which female gametes are produced.
oogenesis
female gametes produced by oogenesis; haploid
egg(ovum)
stage of mitosis and meiosis in which daughter chromosomes each opposite poles and nuclei are formed. cytokinesis begins here.
telophase
an organism or cell containing 2 set of chromosomes, each set inherited from each parent
diploid
a process occurring in the male testis in which male gametes are produced
spermatogenesis
the male gamete produced by spermatogenesis: haploid, small and flagellated
spermatozoa
an association of genes consisting of DNA and proteins. used to transport the genetic infomation.
chromosome
sequence of events in the life of a dividing cell consisting of interphase (G1, S, G2) and mitosis
cell cycle
stage of mitosis and meiosis immediately following interphase during which the chromosomes condensed.
prophase
4 chromatids which make up a paired homologous chromosomes in prophase 1 of meiosis 1
tetrad
chromosome pairs of the same length, centromere position, and staining pattern which posses genes for the same traits at corresponding loci. one is inheritied from the mother and one form the father.
homologous chromosomes
earlobes
free - dominant
attached - recessive
albinism
autosomal recessive
tongue rolling
can - dominant
can't - recessive
cystic fibrosis
autosomal recessive
taysachs diseases
autosomal recessive
sickle cell anemia
codominant
homozygous you have it, hetero you have the trait
hypercholesterolemia
codominant
achondroplasia
autosomal dominant
RR - dead
Rr - dwarf
rr - normal
huntingtons disease
autosomal dominant
late acting
alzheimers disease
autosomal dominant
any detectable phenotype of a particular inherited character
trait
trait of a certain species seen in each generation varying only by mutation
true-breeding
a specific region on a chromosome coding for a specific gene
locus
haploid cell (usually egg or sperm) that unites with another haploid cell during fertilization to form a zygote
gamete
a breeding experiment in which a single traits is followed
monohybrid
breeding experiment in which 2 traits are studied
dihybrid
any detectable phenotype of a particular inherited character
trait
the parental generation of a breeding experiment producing the original gametes
P generation
1st generation offspring of a breeding experiment
F1 generation
trait of a certain species seen in each generation varying only by mutation
true-breeding
2nd generation offspring of a breeding experiment
F2 generation
alternative form of a gene
allele
form of a gene which is always expressed in a heterozygote
dominant allele
form of a gene which is masked in a heterozygote
recessive allele
Mendels first law explaining the separation of alleles when gametes are synthesized and then randomly paired again at fertilization; monohybrid cross
law of segregation
gene has 2 of the same alleles for a given trait
homozygous
gene with 2 different alleles for a given trait
heterzygous
physical expression of an organisms genetic makeup
phenotype
genetic description of an organism
genotype
in order to discover the unknown genotype of an organism, it is bred with a homozygous recessive individual so that the alleles will be expressed in the F1 generation
testcross
derived from a dihybrid cross. each allele pair segregate independently during gamete formation
law of independent assortment
XO
meiosis in egg or sperm formation
sex organs do not mature, sterile, and short of stature
turner syndrome
female
xxx
meiosis in egg formation
limited fertility
metafemale
3 chromosomes at 21
aneuploidy
severe mental retardation
trisomy 21
down syndrome
XXY
meiosis in egg or sperm
testes abnormally small, sterile, and feminine body characteristics
klinefelter syndrome
male
XYY
meiosis in sperm
normal male
phenotypically normal male
discovered and created modes of inheritance, law of segregation and law of independent assortment, while studying garden pea plant
Gregor Mendel
american genecist and zoologist who discovered sex linkage traits during study of fruitflies
Thomas Hunt Morgan
study indian corn led to discover mobile genetic elements known as "jumping genes" or transposable elements. 1st proof genes can change locations on a chromosome
Barbara McClintock
1st woman to receive unshared Nobel Prize
pattern of inheritance resulting from genes located on the X chromosomes
sex linkage
common usually dominant trait in a natural population
wild type
a phenotype which varies from the parentals due to mutation or crossing over
mutant phenotype
pea plane studies by Gregor Mendel to determine the mode of inheritance
pisum sativum
when an organisms XY chromosome arrangement is male and XX chromosome arrangement is female
homogametic
when an organisms XY chromosome arrangement is female and XX chromosome is male
heterogametic
when homologous chromosome or sister chromatids fail to separate in mitosis or meiosis
non-disjunction
development of an egg without fertilization
parthenogenesis
the fruitfly used in breeding experiments to determine modes of inheritance
drosophila melanogaster
cell with a single set of chromosomes
haploid
cell with 2 sets of chromosomes each from a different parent
diploid
when cells have one extra or one less chromosome. autosomal aneuploidy is usually fatal to humans and is linked to most miscarriages
aneuploidy
genetic exchange between 2 homologous chromosomes
crossing over
British scientists who retrieved date which did not correspond to classic Mendelian ratios; led to the discovery of linkage and crossing over
Bateson and Punnett
scientist who used Drosophila to discover the phenomenon of sex linkage and crossing over
TH Morgan
species of fruitly used in genetic crosses; aided in the discovery of sex linkage, crossing over and many other genetic phenomena
Drosophila melanogaster
one of Mendels laws where pairs of alleles assort independently of other sets of alleles. Demonstrated by Mendels peas using dihybrid crosses
independent assortment
genes found on the same chromosomes
linked genes
offspring with phenotypes differing from the parents; a result of crossing over
recombinants
spacial representation of locations of genes on a chromosome derived from probability of crossing over
gene maps
1% crosing over - one map unit (centiMorgan). not an actual measurement of distance
map units