diversity, classification and variation Flashcards
what is a gamete?
reproductive cells. they joint together to form a zygote
what does diploid and haploid mean?
diploid means that the cells have two of each chromosome, in a haploid cell there is only one copy of each chromosome humans have 46 chromosomes - 23 chromosome pairs
explain the idea of random fertilisation
any sperm can fertilise any egg. it can produce zygotes with different combinations of chromosomes to both parents. this icing of genetic material increases the genetic diversity within a species
what is meiosis?
meiosis is a type of cell devision. it takes place in the reproductive organs
describe the process of meiosis I
Interphase - the DNA unravels and replicates so that there are two copies of each chromosome called chromatids
Prophase I - the DNA condenses to form a double armed chromosome made from sister chromatids which are joined in the middle via a centromere. each of these chromosomes joins up with its homologous partner to form a tetrad
Metaphase I - spindle fibres attach to each of the homologous CHROMOSOMES
Anaphase I - the fibres contract and pull the chromosomes to opposite ends of the cell this halves the number of chromosomes.
describe the process of meiosis II
Metaphase II - the chromatids line up in a similar way to that of mitosis. the spindle fibres attach to the centromeres
Anaphase II - the sister chromatids separate and move toward opposite ends of the cell
Telophase II - meiosis II results in four haploid daughter cells
give three reasons why sexual reproduction gives varied offspring
crossing over - prophase I
independent assortment - Metaphase I
random fertilisation
wat is synapsis?
where homologous chromosomes come together to form a tetrad - these chromosomes carry the same genes at the same loci
what is chromosome closing over?
during Prophase I homologous chromosomes come together and pair up. the chromosomes twist around each other and its of chromatids swap over, the chromosomes still have the same genes but they now have different combinations of alleles
what is the process of independent segregation?
each homologous pair of chromosomes in a cell is made up of maternal and paternal chromosomes. when they are separated it is completely random which ends up un the daughter cell. so the four daughter cells produced have completely different combinations of maternal and paternal chromosomes.
what is the mutation non-disjunction?
the failure of the chromosomes to separate properly. this can lad to down syndrome.
what is down syndrome?
it is caused by a person having an extra copy o the chromosome 21 so one cell gets an extra copy of 21 and another gets none
what is substitution?
when one base is substituted with another
what is deletion?
when one base is deleted
what do mutations mean?
the order of bases in the DNA codes for specific amino acids. a mutation within these bases could alter the sequence of amino acids. however due to the degenerate nature of the genetic code more than one DNA triplet codes for one amino acid meaning that not all substitutions will result in a change however deletions will (it will cause a shift in all of the bases after it)
what will mutagenic agents do?
they increase the rate of mutation
e.g. ultraviolet light, ionising radiation and smoking the tar in cigarettes.
what can increase the genetic diversity within a population?
Mutations in the DNA
gene flow - different alleles being introduced into a population from another population which has migrated into them and reproduced
what is a genetic bottleneck and what does it do?
an event that causes a big reduction in a population. this reduces the number f different alleles in the gene pool and so reduces genetic diversity.
what is the founder effect?
the founder effect describes what happens when just a few organisms dorm a population start a new colony ans there are only a small number of different alleles in the initial gene pool. the frequency of each allele in the new colony might be very different to the frequency of those allies in the original population. the risk of genetic disease is therefore increased.