Summary Flashcards From Website
What is the difference between interspecific variation and intraspecific variation?
Interspecific = variation that exsists between different species. E.g. the difference between horses and ducks.
Intraspecific = The differences that occur within a species e.g. the length of giraffes necks
Explain the two factors that cause variation
1) genetic = individuals within a species can have different versions of those genes called alleles. The alleles an organism has make up its genotype. Different genotypess result in variation in phenotype - the characteristics displayed by an organism. For example eye colour, or blood type.
Environmental = The appearance (phenotype) of an invidividual is also affected by the environment. For example plant growth in affected by the amount of minerals available in the soil or in identical twins, they have the same alleles may have had different illnesses in their childhood or if they grew up in different areas, have different accents.
Why does the sample have to be random when studying variation and give an example on how they make it random?
To make sure the sample isn’t biased.
If you were looking at plant species in a field you could pick random sample sites by dividing the field in a grid and using a random number generator to select co ordinates
What does the standard deviation of data tell us?
It tells you how much the values in a single sample vary, its a measure of the spread of values about the mean.
A large standard deviation means the values in the sample vary a lot. A small standard deviation tells you most of the sample data is round the mean value so varries little.
What are the three main components of nucleotides?
1) A deoxyribose sugar (stays the same)
2) a phosphate group (stays the same)
3) nitrogenous base (varies)
Describe how DNA is different in Eukaryotic cells and prokaryotic cells
Prokaryotic cells = DNA molecules are shorter and circular, it isn’t wound around proteins
Eukaryotic cells = The DNA is linear, really long and wound around proteins.
How are Nucleotides joined together?
1) DNA nucleotides join together to form polynucleotide strands
2) The nucleotides join up between the phosphate group of one nucleotide and the sugar of another creating a sugar-phosphate backbone
3) Two DNA polynucleotide strands join together by hydrogen bonds between the bases
4) Each base can only join with one particular partner - this is called specific base pairing
5) Adenine always pairs with thymine and guanine always pairs with cytoside
6) The two strands wind up to form the DNA double-helix
How can a mutation result in a non-functional enzyme?
1) mutations are changes in the base sequence of an organisms DNA
2) mutations produce new alleles of genes
3) A gene codes for a particular protein, so if the sequence of bases in a gene changes, a non-functional or different protein could be produced.
4) All enzymes are proteins, if theres a mutatio in a gene that codes for an enzyme, the enzyme may not fold up properly. There will be a change in the enzymes secondary and tertiary structure and the active site will be the wrong shape which will end up in a non-functional enzyme.
What is an intron?
Sections of DNA which don’t code for amino acids.
Introns are removed during protein synthesis.
What is a homologous pair of chromosomes?
Pairs of matching chromosomes
In a homologous pair, both chromosomes are the same size and have the same genes although they could have different alleles.
Explain the two ways meiosis produces variation
1) crossing over of chromotids = The crossing over of chromotids in meiosis I neabs that each of the four daughter cells formed from meiosis contrain chromatids with different alleles
2) Independent assortment of chromosomes = The four daugher cells formed from meiosis have completley different combinations of chromosomes, All your cells have a combination of chromosomes, half from your mum (maternal) and half from your dad (paternal) When the gametes are produced, different combinations of those maternal and paternal chromosomes go into each cell. This is called independent assortment of chromosomes.
Explain the process of meiosis
1) The DNA unravels and replicates so there are two copies of each chromosome called chromotids.
2) The DNA condenses to form double-armed chromosomes, made from two sister chromotids
3) Meiosis I - the chromosomes arrange themselves into homologous pairs
4) These homologous pairs are then seperated halving the chromosome number
5) Meiosis II - the pairs of sister chromotids that make up each chromosome are seperated
6) four haploid cells that are genetically different from each other are produced.
Identify two arguments against and two arguments for selective breeding.
Arguments for selective breeding:
1) It can produce high yielding animals and plants
2) It can be used to produce animals and plants that have increased resistance to disease
Arguments against selective breeding:
1) It can cause health problems to the animals
2) It reduces genetic diversity
How does the founder effect reduce genetic diversity?
The founder effect is when just a few organisms from a population start a new colony. Only a small number of organisms have contributed their alleles to the gene pool. A narrower range of alleles lead to lower genetic diversity.
How do genetic bottlenecks reduce genetic diversity?
A genetic bottle neck is an event that causes a big reduction in a population e.g when a large number of organisams within a population die before reproducing. This reduces the number of different alleles in the gene pool and so reduces genetic diversity. The survivors reproduce and a larger population is created from a few individuals.
How does selective breeding reduce genetic diversity?
Selective breeding leads to a reduction in genetic diversity - once an organism with the desired characteristics has been produced, only that type of organism will continue being bred,.
It results in a type of genetic bottle neck as it reduces the number of alleles in the gene pool.
How is oxygen carried round the body by haemoglobin?
1) Haemoglobin has a high affinity for oxygen - each molecule can carry four oxygen molecules
2) In the lungs, oxygen joins to haemoglobin in red blood cells to form oxyhaemoglobin
3) This is a reversible reaction - when oxygen leaves oxyhaemoglobin near the body cells, it turns back to haemoglobin.
How does the carbon dioxide concentration affect oxygen unloading?
1) when cells respire they produce carbon dioxide, which raises the pCO2
2) This increases the rate of oxygen unloading - the dissociation curve shifts down. The saturation of blood with oxygen is lower for a given pO2 meaning that more oxygen is being released
3) This is caused the Bohr effect
How is haemoglobin different in different organisms?
1) organisms that live in environments with a low concentration of oxygen have haemoglobin with a higher affinity for oxygen than human haemoglobin - the dissociation curve is to the left of ours
2) Organisms that are very active and have a high oxygen demand have haemoglobin with a lower affinity for oxygen than human haemoglobin - the curve is to the rightof the human one.
Explain how haemoglobin load and unload in the body?
1) The partial pressure of oxygen is a measure of oxygen concentration. The greater the concentration of dissolved oxygen in cells, the higher the partial pressure
2) Similarly , the partial pressure of carbon dioxide is a measure of the concetration of CO2 in a cell.
3) Haemoglobins affinity for oxygen varies depending on the partial pressure of oxygen.
4) oxygen loads onto haemoglobin to form oxyhaemoglobin where theres a high PO2, oxyhaemoglobin unloads its oxygen where theres a lower pO2
5) oxygen enters blood capillaries at the alveoli in the lungs. Alveoli have a high PO2 so oxygen loads onto haemoglobin to form oxyhaemoglobin
6) when cells respire, they use up oxygen - this lowers pO2, Red blood cells deliver oxyhaemoglobin to respiring tissues, where it unloads its oxygen.
7) The haemoglobin then returns to the lungs to pick up more oxygen.