4B Diversity, Classification and Variation Flashcards

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1
Q

What is genetic diversity?

A

Genetic diversity is the number of different alleles of genes in a species or population.

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2
Q

How can genetic diversity with in a population increase?

A

Different alleles can be introduced into a population by individuals from another population which migrate into them and reproduce. This is known as gene flow

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3
Q

What does genetic diversity allow for which is needed for evolution?

A

Natural selection

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4
Q

What is a genetic bottleneck?

A

A genetic bottleneck is an event that causes a big reduction in a population, e.g. when a large number of organisms wthin 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.

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5
Q

Explain how a genetic bottle neck leads to decreased genetic variation.

A

The genetic bottleneck reduces the number of different alleles in the gene pool because certain types of alleles in the population of organisms will have a lower or higher chance of surviving the event that causes mass death to the population.

As a result of this, the organisms with the best alleles suited for survival are the most likely to survive the genetic bottleneck and be part of the very small population at the end of the event. And vice versa, the organisms with the worse alleles suited for survival are much more likely to die and so have a lower chance to pass the allele, even with the chance of extinction for that certain characteristic.

The organisms will then reproduce to bring numbers back up after the event, and because a majority will now have the favorable allele due to natural selection, allowing them to survive, a high majority of the population will have not much genetic diversity between them, with some alleles before the genetic bottleneck even becoming extinct.

Here’s a good image to help: https://d20khd7ddkh5ls.cloudfront.net/bottleneck_effect_3.jpg

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6
Q

Briefly describe natural selection.

A

Natural selection is a mechanism of evolution. Organisms that are more adapted to their environment are more likely to survive and pass on the genes that aided their success. This process causes species to change and diverge over time.

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7
Q

Explain the process of natural selection.

A

A gene mutation occurs within an organism in a species which positively benefits the organism.

Since there is competition for food and resources, individuals that have an allele that increases their chance of survival are more likely to survive, reproduce and pass on their genes (including the beneficial allele) than the organisms which do not have the allele.

This means that a greater proportion of the next generation inherits the beneficial allele.

They, in turn are the most likely to survive, reproduce and pass on their genes.

So the frequency of the beneficial allele increases from generation to generation.

Over generations, this leads to evolution as the advantageous alleles become more common in the population.

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8
Q

What is variation?

A

Variation is the differences between characteristics of the same species.

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9
Q

Tawny owls show variation in color. There are light grey and darker brown owls.

Before the 1970s, there were more grey owls than brown owls in Finland. Since then, climate change has been causing a decrease in the amount of snowfall in Finland. During this period, the darker brown owls have become more common.

Suggest why the brown owls are better adapted to being in an area with less snowfall than the grey owls.

Explain how the brown owls have become more common.

A

The reason why brown owls are adapted to being in an area with less snowfall than grey owls is because they benefit from camouflage - brown owls are able to better blend into the ground with less snowfall, making them much harder to detect and so become more stealthy, increasing their chances of survival.
Grey owls will suffer from less snowfall as they will have less time to camouflage and so they will be more open to attacks from predators as they are much easier to spot as they will not blend into the environment as often, making the chance of survival lower.

In a population, there are grey owls and brown owls. Initially, the rate of snowfall in Finland was high, but after the 1970s, the rate of snowfall in Finland decreased, causing an increase in brown owls.

This is because, as the rate of snowfall decreases, the brown owls will find it much easier to compete for food against it’s grey counterpart as the presence of snow, which once offered camouflage to the grey owls, has decreased, lowering their chances of survival. In contrast, the brown owls did not benefit from the presence of snowfall, and so the decrease in the rate of snowfall will allow them to have a higher chance of survival. This is because the camouflage for brown owls are increasing following the decrease in snowfall compared to the grey owls, which are decreasing.

The brown owls will find it increasingly easier to hunt for food as predators find it harder to spot them, and so will have a higher chance to survive, leading to offspring which will pass down the beneficial allele, which over generations will increase the presence of the allele in the population as it is advantageous, leading to a higher presence of brown owls.

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10
Q

Define directional selection.

A

Directional selection is a type of natural selection where the the individuals with a certain allele are more likely to reproduce than before, causing the allele frequency to shift in one direction, responding from something like an environmental change.

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11
Q

Define stabilizing selection.

A

Stabilizing selection is a type of natural selection where the individuals with a certain allele that has the best chance of survival in the environment end up taking up a very high percentage of the population as the environment is not changing, and so a very high amount of the population have the same combination of allelles for a certain characteristic.

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12
Q

Give an example of directional selection.

A

Antibiotic resistance

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13
Q

Describe how antibiotic resistance causes directional selection, starting from when the antibiotic is introduced into the population.

A

Firstly, the antibiotic will be introduced into the population of bacteria.

Mutations in the genes of bacteria will allow some bacteria to have immunity to that certain antibiotic. At this point, the antibiotic resistant bacteria will be a minority of the population.

The antibiotic will kill almost all the bacteria which do not have the mutation required to be resistant to the antibiotic.

The resistant bacteria will have almost no competition for food or resources after the antibiotics wipe out most of the population, allowing it to survive and reproduce with a much higher chance.

The resistant bacteria, since it is more likely to survive, has a much higher chance to reproduce and pass on offspring with the genes that have antibiotic resistance.

As a result of this, after multiple lifecycles of bacteria, the antibiotic resistant bacteria will be the majority in the population, compared to before the antibiotic was introduced to the population.

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14
Q

In some farms, animals are often given antibiotics in their food.

Scientists investigated whether those farm animals had antibiotic-resistant bacteria in their intestines. They tested the bacteria for resistance to two antibiotics, tetracycline and streptomycin.

29% of bacteria had resistance to Tetracycline.
13% of bacteria had resistance to streptomycin.

Suggest and explain a reason why there is a difference in results of antibiotic resistance.

A

Because Tetracycline might’ve been used more often than streptomycin, causing a higher rate of antibiotic resistance within the population.

or:

Because there might be a higher frequency for mutations which offer resistance to Tetracycline compared to Streptomycin, causing a higher rate of initial antibiotic resistance. This increases the rate of antibiotic resistance within the population further on.

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15
Q

Bacterial meningitis is a potentially fatal disease affecting the membranes around the brain. Neisseria meningitidis (Nm) is a leading cause of bacterial meningitis.

Penicillin has been the antibiotic of choice for the treatment of bacterial meningitidis. Since the year 2000, strains of Neisseria meningitidis that are resistant to penicillin and other antibiotics have been discovered in the UK.

Describe how a population of Neisseria meningitidis (Nm) can because resistant to these antibiotics.

A

A mutation within the population of Neisseria meningitidis might occur which offers bacterial resistance to an antibiotic, for example, Penicillin.

When the population of Neisseria Meningitidis becomes exposed to penicillin, the minority population with the antibiotic resistant gene will survive while most of the other bacteria will be wiped out.

Since the antibiotic resistant bacteria are one of the few surviving, there is much less competition between other bacteria for food and resources. Therefore, it is much easier to survive and reproduce.

Due to the increase in reproduction of this certain antibiotic resistant bacteria, this will cause an increase in the population of the bacteria which express the gene needed for antibiotic resistance.

As a result of multiple generations of bacteria being exposed to penicillin, the majority of Neisseria meningitidis in that population will have inherited the gene needed for antibiotic resistance as a result, becoming the majority of the population.

This process will repeat and apply for every single antibiotic in the list given until the population of bacteria will be resistant to all 3 antibiotics listed.

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16
Q

What is a gamete?

A

Gametes are an organism’s reproductive cells. For example, sperm and egg cells in humans.

They join together at fertilization to form a zygote, which develops into a new organism.

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17
Q

What is a diploid cell?

A

A diploid cell has 2n chromosomes.

This means that the cell contains two copies of each chromosome.

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18
Q

Are normal body cells diploid or haploid?

A

Diploid

The cells have two copies of each chromosome.

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19
Q

Are gametes haploid or diploid?

A

Haploid

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20
Q

What is a haploid cell?

A

A haploid cell has ‘n’ chromosomes.

This means the cell contains only one copy of each chromosome.

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21
Q

Label A,B and C as either haploid or diploid cells:

https://media.discordapp.net/attachments/352951793187029005/813121102581596170/unknown.png?width=608&height=562

A

A = Diploid

B = Diploid

C = Haploid

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22
Q

Describe what happens in fertilization between a sperm and egg cell.

A

A haploid sperm fuses with a haploid egg, making a cell with the normal diploid number of chromosomes, known as a zygote.

Half of these chromosomes are from the father, and half are from the mother.

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23
Q

Describe how fertilization increases genetic diversity.

A

During sexual reproduction, any sperm can fertilize any egg - fertilization is random.

Random fertilization produces zygotes with different combinations of chromosomes to both parents.
This mixing of genetic material in sexual reproduction increases genetic diversity within a species.

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24
Q

What is Meiosis?

A

Meiosis is a type of cell division that takes place in the reproductive organs, wherein the product are four genetically different daughter cells.

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25
Q

Two gametes fuse together to create a zygote.

Does the zygote become diploid or haploid? Describe how.

I would recommend trying to draw this out, showing the chromosome contents from both gametes into the zygote and what becomes of it.

A

A gamete from the father (sperm) and a gamete from the mother (egg) are both haploid, meaning that they only have one of each chromosome.

At fertilization, when the sperm fuses with the egg, a cell is made with the normal diploid number of chromosomes, having two of each chromosome, wherein half is from the father and the other half is from the mother.

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26
Q

Describe what happens to a reproductive cell right before meiosis happens.

A

The cell unravels its DNA, replicating it in the process, creating two copies of each chromosome (2 x 2n).

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27
Q

What does ‘n’ mean?

A

The cell contains only one copy of each chromosome.

Haploid

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28
Q

What does ‘2n’ mean?

A

The cell contains two copies of each chromosome.

Diploid

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29
Q

What does ‘2 x 2n’ mean?

A

The cell contains two copies of each chromosome, which are double armed chromosomes as they have two chromatids joined by a centromere.

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30
Q

Describe the process of meiosis.

A

Before meiosis, the cell replicates and unwinds it’s DNA, doubling the amount of chromosomes it contains.

The cell then condenses it’s DNA, forming double armed chromosomes, each made up of two sister chromatids joined up by a centromere and in homologous pairs.

The cell then goes through the first meiotic division, wherein the cell divides, separating the homologous pairs apart and halving the number of double armed chromosomes in each of the two cells, meaning there is now only one pair of each chromosome in each cell.

The cell then goes through the second meiotic division, wherein the two cells divides to create, in total, 4 new, genetically different daughter cells which are haploid, meaning that they have only one copy of each chromosome.

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31
Q

Describe the process of crossing over.

A

The process of crossing over occurs in the first round of meiotic division, wherein each homologous pair of chromosomes come together and pair up.

From there, the chromatids nearest to each chromosome in the pair twist around each other and bits of chromatids swap over, forming a bivalent.

The chromatids still contain the same genes, but can now have a different combination of alleles, increasing genetic variation.

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32
Q

Describe what independent segregation refers to, as well as how it increases genetic diversity.

A

Each homologous pair of chromosomes consist of one chromosome from the dad (paternal) and one chromosome from the (mum).

During the first round of meiotic division, the homologous pairs are separated, and independent segregation refers to the fact it’s completely random which chromosome from each pair comes into which daughter cell.

So the four daughter cells produced by meiosis have completely different combinations of those maternal and parental chromosomes.

This ‘shuffling’ of chromosomes leads to genetic variation in any potential offspring.

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33
Q

Describe how crossing over leads to increase genetic variation.

A

During crossing over, non-sister chromatids are exchanged with each other in a homologous pair.

Crossing over creates new combinations of genes in the gametes that are not found in either parent, contributing to genetic diversity.

As well as this, crossing over ensures that each gamete produced as a result of meiosis have different chromatids to each other, and therefore a different set of alleles, which increases genetic variation.

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34
Q

This diagram features the process of meiosis.

Fill in the graph:

https://media.discordapp.net/attachments/352951793187029005/814602641765302322/unknown.png?width=467&height=563

Only show 2 chromosomes, not all 23.

A

https://media.discordapp.net/attachments/352951793187029005/814603271405568050/unknown.png?width=485&height=563

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35
Q

Does crossing over occur in Meiotic division 1 or 2?

A

Meiotic division 1

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36
Q

Give two differences between Meiosis and Mitosis.

A

Differences:

Meiosis produces 4 daughter cells. Mitosis produces 2.

Meiosis produces genetically different daughter cells. Mitosis produces genetically identical daughter cells.

Meiosis produces cells with half the number of chromosomes than the parent cell.
Mitosis produces cells with the same number of chromosomes as the parent cell.

Meiosis has 2 nuclear divisions, Mitosis is 1.

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37
Q

The fertilization of a gamete that causes down syndrome must mean it has what features?

A

The gamete must have two of the same chromosome, wherein it must be chromosome 21.

This ensures the gamete, when fertilized with the sperm will achieve an extra chromosome 21, having three, than the usual two, causing down syndrome.

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38
Q

How is a chromosome mutation caused?

A

Errors during meiosis

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39
Q

What do chromosome mutations lead to, granted that the mutated gamete gets fertilized?

A

Chromosome mutations lead to inherited conditions because the errors are present in the gametes which will divide by mitosis holding the error for the rest of its life.

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40
Q

Give one type of chromosome mutation.

A

Non-disjunction

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41
Q

Describe what happens in a non-disjunction event.

A

A non-disjunction event is the failure for chromosomes to separate properly.

42
Q

Describe how is down’s syndrome is caused, from the meiotic division 1, to meiotic division 2 and fertilization.

A

Down syndrome is caused by a non-disjunction event of chromosome 21 during the first meiotic division - it causes the homologous pair of chromosomes to fail to separate and both chromosomes end up in a single cell.

In order for down syndrome to be caused, meiotic division 2 must happen which creates two gametes with the chromosome mutation of two chromosome 21’s rather than only one for each cell, and it must be fertilized, meaning that the gamete is ended up being given an extra copy of chromosome 21, leading to down’s syndrome.

43
Q

Fill in the graph to identify how an individual can get down’s syndrome:

https://media.discordapp.net/attachments/352951793187029005/814606715504033882/unknown.png?width=1282&height=563

Assume that the chromosome(s) you will be drawing are/is chromosome 21.

A

https://media.discordapp.net/attachments/352951793187029005/814607125333540864/unknown.png?width=1255&height=562

44
Q

Outline how Patau’s syndrome is caused.

A

Patau’s syndrome is caused from a non-disjunction event happening between chromosome 13 during Meiosis meaning that a gamete, or multiple gametes end up having an extra chromosome 13.

If the gamete with an extra chromosome 13 gets fertilized into a zygote, it ends up having 3 of chromosome 13 than 2, meaning when it begins to divide by Mitosis, most if not all body cells will have the extra chromosome, leading to Patau’s syndrome.

45
Q

Briefly outline how Down’s syndrome is caused.

A

Down’s syndrome is caused from having an additional copy of chromosome 21 in some or all body cells.

46
Q

What phase of Meiosis is this?

https://media.discordapp.net/attachments/352951793187029005/814938154968547370/unknown.png

A

Interphase

47
Q

What phase of Meiosis is this?

https://media.discordapp.net/attachments/352951793187029005/814938203760230431/unknown.png

A

Prophase 1

48
Q

What phase of Meiosis is this?

https://media.discordapp.net/attachments/352951793187029005/814938241878065222/unknown.png

A

Metaphase 1

49
Q

What phase of Meiosis is this?

https://media.discordapp.net/attachments/352951793187029005/814938292620886047/unknown.png

A

Anaphase 1

50
Q

Describe what happens in Telophase 1 of Meiosis.

A

In Telophase 1 of Meiosis, Chromosomes decondense and the single cell divides by cytokinesis, with a nuclear envelope reforming in both new daughter cells.

Both cells have half the chromosome count of the initial cell.

51
Q

What phase of Meiosis is this?

https://media.discordapp.net/attachments/352951793187029005/814938445666451476/unknown.png

A

Prophase 2

52
Q

What phase of Meiosis is this?

https://media.discordapp.net/attachments/352951793187029005/814938476310167623/unknown.png

A

Metaphase 2

53
Q

What phase of Meiosis is this?

https://media.discordapp.net/attachments/352951793187029005/814938506412425236/unknown.png

A

Anaphase 2

54
Q

Describe what happens in Telophase 2 of Meiosis.

A

In Telophase 2, both the cells involved have their chromosomes decondense, becoming long and thin again. The cell then divides by cytokinesis, while the nuclear envelope reappears.

The product of Telophase 2 are four genetically different daughter cells.

55
Q

What happens in Prophase 1?

A
In Prophase 1, the cell's chromosomes
condense, becoming shorter and fatter.
Homologous chromosomes join up into
homologous pairs, going close to each 
other, becoming held by a bundle of 
protein called a centromere and forming bivalents by swapping their sister chromatid over with another non-sister chromatid to swap over alleles called crossing over.

Centrioles move to opposite poles of
the cell, and the nuclear envelope dissolves.

56
Q

What happens in Metaphase 1?

A

In Metaphase 1, spindle fibers from opposing centrioles connect to the bivalent chromosomes by their centromere and the chromosomes align themselves to the middle of the cell attached to their homologous pair in a bivalent.

57
Q

What happens in Anaphase 1?

A

In Anaphase 1, the spindle fibers contract, splitting the centromere and separating the pairs of homologous bivalent chromosomes to opposite poles of the cell.

58
Q

What happens in Prophase 2?

A

The chromosomes condense, becoming shorter and fatter. Tiny protein bundles called centrioles arrive to opposite poles of the cell, perpendicular to Prophase 1.

The nuclear envelope also dissolves.

59
Q

What happens in Metaphase 2?

A

Spindle fibers from opposing centrioles attach to the chromosomes present by their centromere, aligning them to the equator of the cell.

60
Q

What happens in Anaphase 2?

A

The spindle fibres contract, separating the sister chromatids from the initial double armed chromosomes, moving to opposite poles of the cell.

61
Q

Describe how Meiosis achieves genetic variation.

A

Meiosis features independent segregation, wherein during the separation of the homologous chromosomes, the combination of maternal and paternal chromosomes that end up in one of the two cells during the first meiotic division is completely random.

This means that the four daughter cells produced in meiosis have completely different combinations of maternal and paternal chromosomes, ensuring
variation in any potential offspring.

As well as this, Meiosis features something called crossing over, which occurs during Prophase 1 to each homologous pair of chromosomes in the
cell.

The homologous pair of chromosomes in this instance will form a bivalent, swapping over contents of their chromatids with each other to achieve different combinations of alleles while keeping the same genes as they are homologous.
This achieves variation, as it guarantees that the end product of meiosis, the four genetically different daughter cells, will all have a different
combination of alleles.

62
Q

Figure 1 shows the chromosomes in a diploid cell:

https://media.discordapp.net/attachments/352951793187029005/814970155963514960/unknown.png

Complete figure 1 to show the four different combinations of these chromosomes in the gametes produced by Meiosis.

A

https://media.discordapp.net/attachments/352951793187029005/814970975191826442/unknown.png

63
Q

What is a substitution mutation?

A

A substitution mutation is when one base is substituted with another, e.g. ATGCCT becomes ATTCCT (G is swapped for T).

64
Q

What is a deletion mutation?

A

A deletion mutation is when one base is deleted, e.g. ATGCCT becomes ATCCT (G is deleted).

65
Q

In a gene, a substitution mutation occurs.

Using your knowledge about the features of DNA, describe why there may be no changes in the amino acid being coded for even after the mutation.

A

This is due to the fact that the genetic code in DNA is degenerate - with 20 amino acids and 64 possible base pairs, codons can code for multiple amino acids, meaning a substitution mutation in one codon can still allow it to code for the same amino acid.

Take this for an example,

Code: TAT AGT
Mutated code: TAC AGT

T is substituted with C.
To code for Tyrosine, you need TAT and TAC.
Both codes still code for tyrosine.

66
Q

A deletion mutation occurs in a gene that codes for a polypeptide.

Will this deletion mutation guarantee a change in the amino acid sequence?

A

Yes, because the deletion of a base will change the number of bases present.

67
Q

What is a Mutagenic Agent?

A

A mutagenic agent is something that is capable of speeding up the rate of DNA mutation.

DNA mutation is often occuring spontaneously, but certain things, such as ionizing radiation and even viruses, can speed up the rate of DNA mutation, therefore they are called mutagenic agents.

68
Q

What is a gene mutation?

A

Gene mutations involve a change in the DNA’s base sequence, which can be caused when DNA is misread during replication.

69
Q

Figure 1 shows a DNA base sequence. It also shows the effect of two mutations on this base sequence.

Figure 2 shows DNA triplets that code for different amino acids:

https://media.discordapp.net/attachments/352951793187029005/815314666422796369/unknown.png

Complete figure 1 to show the sequence of amino acids coded for by the original DNA base sequence.

A

Ile - Gly - Val - Ser

70
Q

Some gene mutations affect the amino acid sequence, and some mutations do not.

Use the information from Figure 1 and Figure 2 to explain whether mutation 1 affects the amino acid sequence.

https://media.discordapp.net/attachments/352951793187029005/815314666422796369/unknown.png

A

Mutation 1 will not affect the amino acid sequence, as the degenerate structure of the genetic code means that with 20 amino acids and 64 combinations of base pairs, codons can code for more than one amino acid.

This is supported by the fact that the mutation occuring in mutation 1 still codes for Glycine, and so there will be no change in the amino acid sequence and primary structure of the polypeptide produced.

71
Q

Figure 1 shows a DNA base sequence. It also shows the effect of two mutations on this base sequence.

Figure 2 shows DNA triplets that code for different amino acids:

https://media.discordapp.net/attachments/352951793187029005/815314666422796369/unknown.png

Describe how mutation 2 can lead to the formation of a non-functional enzyme.

A

Mutation 2 could lead to the formation of a non-functional enzyme, due to the fact that it codes for Leucine rather than Valine, therefore changing the amino acid sequence of the enzyme, which in turn affects the primary structure of the enzyme and as well as the tertiary structure of the enzyme, wherein it could lose the ability to form an enzyme-substrate complex properly due to the fact that the active site has changed in shape,

Therefore losing its ability to function properly.

72
Q

A vole is a small, mouse like animal. Voles found on some cold islands to the north of Scotland are much larger than voles found in warmer areas such as southern France. Explain how natural selection may have caused the northern voles to be larger in size.

A

Firstly, the Voles in cold islands compete for food and resources in order to survive so they can reproduce.

DNA mutations occur within the population of Voles, wherein some will be larger than others.

Larger Voles would have the best chance of survival in cold islands, due to the fact that their surface area to volume ratio decreases, meaning that less heat is expelled from them when they are
in a cold environment, meaning it becomes easier to maintain body heat. As well as this, less energy is needed in order to maintain body heat due to
the fact that metabolism is decreased as heat does not have to be generated as fast to maintain a stable temperature.

As a result of this, the larger Voles will have the highest chance to survive as they will be able to hunt for food the longest while maintaining their body heat, therefore being able to make it to adulthood and pass on their desirable alleles to their offspring, making the offspring larger and over time, through multiple generations of
reproduction, evolution occurs where the majority of the voles in the population will have the allele
which supports a larger size.

The size can increase through more DNA mutations that make the voles even bigger, repeating this process.

73
Q

Great tits are small birds. Female great tits usually lay between 3 and 14 eggs in a nest. Natural selection influences the number of eggs laid. Explain why great tits that lay fewer than 3 eggs per nest or more than 14 eggs per nest are at a selective disadvantage.

A

Great tits that lay under 3 eggs are at
a selective disadvantage due to the fact
that too little offspring were produced -
generally, offspring from birds are
extremely attractive bait for predators
so if one offspring is eaten, that is
extremely punishing for the mother bird,
as it means that they only have one, if
not no more and therefore the offspring
that carried the alleles that determined
the amount of eggs produced generally wont
have a high chance to survive to adulthood.

Great titds that lay over 14 eggs per
nest are at a selective disadvantage
due to the fact that the mother bird may
not be able to provide sufficient food
and resources for all 14 birds and as a
result the mother bird might have to work
harder to give them all food which exposes
them more to predators, increasing the chance
they may die. If the bird is able to
feed the birds, the quantity of food given
to all 14 birds will be much less and
therefore many of them may not be able to
survive through to adulthood as it might
affect their development, decreasing the
chance the alleles for producing over 14
eggs per nest will be passed on to the
next generation.

74
Q

Give an advantage of variation.

A

Variation permits flexibility and survival of a population in response to changing environmental circumstances.

This means that variation increases the chance of a population surviving from certain changes, like a drastically changing environment - for example, if an environment gets more frequent snowfall over time, variation from random DNA mutations will allow the population to adapt and change to the new environment by natural selection.

75
Q

What is a gene pool?

A

A gene pool is the collection of different genes or alleles within an interbreeding population.

76
Q

Apart from genetic factors, what other factors can cause variation within a species?

A

The environment

77
Q

The spotted owl is a bird. Numbers of spotted owls have decreased over the past 50 years. Explain how this decrease may affect genetic diversity.

A

There will be a reduction in genetic diversity as less birds in the population will express different alleles (a reduced gene pool).

78
Q

What is meant by allele frequency?

A

Allele frequency is the rate of occurrence of a certain allele in a population.

79
Q

The figure shows three boxes which shows the distribution of alleles in a sample population.

Calculate the allele frequency of dark grey rats for all three boxes.

https://media.discordapp.net/attachments/352951793187029005/815678968538595348/unknown.png

A

Box 1 = 0.5 (50%)

Box 2 = 0.2 (20%)

Box 3 = 0.0 (0%)

80
Q

A population of 240 rats were reared in a laboratory. They were all fed on a diet containing an adequate amount of vitamin K. In this population, 8 rats had the genotype Ws+Ws, 176 ha the genotype WrWs and 56 had the genotype WrWr.

Use these figures to calculate the allele frequency of the allele Wr in this population. Show your working.

A

240 rats, 480 alleles (body cells diploid)

8 rats = S and S (16 S)
176 rats = R and S (176 R, 176 S)
56 rats = R and R (112 R)

16+176+176+112 = 480

112 + 176 = 288

288 / 480 = 0.6
60%

81
Q

What is a taxon?

A

A taxon is a group featured in one of the eight levels of classification which sorts animals in certain categories of similarity.

82
Q

What is taxonomy?

A

The science of classification. This involves naming organisms and organizing them into groups.

83
Q

Name the three main domans,

A

Archaea, Eubacteria, Eukarya

84
Q

What type of organisms are classified into the Archaea domain?

A

Archaea are a group of single-celled prokaryotic organisms (that is, organisms whose cells lack a defined nucleus) that have distinct molecular characteristics separating them from bacteria.

They are usually known as extremophiles and are seen as extremely ancient.

85
Q

Give an example of an organism in the Archaea domain.

A

Thermophile

86
Q

What type of organisms are classified into the Eubacteria domain?

A

Eubacteria are a group of single-celled prokaryotic organisms known as bacteria.

87
Q

Give an example of an organism in the Eubacteria domain.

A

E Coli

S Aureus

88
Q

What type of organisms are classified into the Eukarya domain?

A

Eukarya are a group of organisms or cells which contain a nucleus enveloped in a nuclear envelope.

89
Q

Give an example of an organism in the Eukarya domain.

A

Human

Plant

90
Q

Name the 8 different taxa.

A
Domain
Kingdom
Phylum
Class
Order
Family
Genus
Species
91
Q

The scientific name of an organism is defined by..?

A

The scientific name of an organism is defined by their Genus, which must be capital, and the species, which must be lowercase.

i.e. Homo sapiens.

92
Q

If you write the scientific name of an organism, describe in what way it must be written whether typing or writing.

A
Typing = it must be in italics
Writing = it must be underlined
93
Q

Name the four Kingdoms in the Eukarya domain.

A

Animalia
Fungi
Protista
Plantae

94
Q

What is the Binomial naming system?

A

The binomial naming system is a globally recognized naming system which gives each organism a unique name in two parts, it’s genus and it’s species in Latin.

95
Q

Give an advantage of the Binomial naming system (nomenclature).

A

It avoids the confusion of using common names, as there are some species which have over 100 organisms in the single group.

96
Q

What is courtship behavior?

A

Courtship behavior is carried out by organisms to attract a mate of the right species.

97
Q

Is courtship behavior species specific?

A

Yes

Only members of the same species will respond to courtship behavior displayed by an organism.

98
Q

Give an advantage of courtship behavior being species specific.

A

Prevents inbreeding as you are able to instantly identify organisms in the same species as you. This is important as breeding with organisms not in the same species as you produces infertile offspring, therefore being useless.

99
Q

What is a species?

A

A species is a group of organisms similar enough to produce fertile offspring.

100
Q

What is a taxon?

A

A taxon represents one of the 8 groups in the system of classification, each of which contains a group of organisms similar to each other, whether by a lot (species) or a little (domain).

101
Q

What is phylogenetic classification?

A

Phylogenetic classification is a type of classification of organisms determined mainly from the homology of DNA to other organisms.

Organisms who share a greater level of homology in their DNA or amino acid sequences are expected to be more closely related.