inheritance, variation, evolution Flashcards

1
Q

what is asexual reproduction

A

only one parent and doesn’t contain any gametes

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2
Q

what is sexual reproduction

A

the fusion of male and female gametes

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3
Q

why do you inherit characteristics from both parents during sexual reproduction

A

because sexual reproduction is the fusion of male and female gametes, the offspring will have a mixture of both genes and therefore have genetic variation

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4
Q

what are gametes and give the three examples

A

cells that carry only have half of the genetic material
eggs and sperm
pollen and eggs

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5
Q

how are gametes made

A

miosis

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6
Q

why is there no genetic variation when asexual reproduction occurs

A

there is only one parent and therefore there is no mixing of genetic material creating identical clones of ofspring

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7
Q

what process do eukaryotes (such as plants and fungi) go through in order to reproduce asexually

A

mitosis

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8
Q

what process do prokaryotes (such as bacteria) go through in order to reproduce asexually

A

binary fission

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9
Q

what are the advantages of asexual reproduction

A

only one parent is needed and the process is very quick
- allows an organism to quickly colonise one area

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10
Q

what are the disadvantages of asexual reproduction

A

no genetic variation - if a new disease comes along and one offspring is susceptible to it its likely that all will be
- also means that they will have less chance of adapting to new conditions like a new climate

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11
Q

what are the advantages of sexual reproduction

A

leads to loads of genetic variation - less likely to get wiped out by a disease (some may be more resistant)
- can adapt to conditions - allow evolution to occur

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12
Q

what are the disadvantages of sexual reproductoin

A
  • takes a lot more time and energy
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13
Q

what is a haploid cell
what is a diploid cell

A

haploid - cells containing half the genetic material of a normal cell
diploid - a cell that has undergone meiosis before fusing to another gamete cell therefore now containing two sets of genetic information from each parent to form an embryo

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14
Q

what is the first steps of meiosis

A
  • replicating all of the cells DNA by replicating the chromosomes - creating an arm for each maternal and paternal chromosome
  • they then line up in the centre of the cell in their pairs
  • chromosomes then pulled to the poles of the cell and the whole cell splits
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15
Q

why is the distribution of DNA different in each cell that undergoes meiosis

A

when lining up in the centre, the chromosomes from the mother and father are in no particular order (left and right order) therefore different each time
- chromosomes are then randomly distributed with each half of the split cell receiving a different combination of maternal and paternal chromosomes

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16
Q

what are the second stages of meiosis

A

the chromosomes line up in the centre of the cell, this time the two arms of the chromosomes will be split to each pole of the cell
- cells then divide in half again
leaving us with four cells

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17
Q

what is the product of meiosis

A

four genetically unique cells that we call gametes that hold 23 chromosomes

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18
Q

what is DNA

A

the chemical all our genetic material is made of and determines what proteins a cell produces

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19
Q

what is DNA made of and what is the structure

A

polymers and is has two strands therefore forming a double helix

the DNA is split into 46 “sections” - chromosomes (which are tight coils) which we have 2x each type

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20
Q

why is the 23 chromosome different

A

they are sex chromosomes
women have two x chromosomes
males have one x and one y

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21
Q

what is a gene

A

a small section of DNA that codes for a particular protein (a sequence of amino acids)
“small segment of a chromosome”

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22
Q

how many different amino acids do we have what do amino acids combine to create

A

20 but they can be interlinked to create 1000s of different proteins

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23
Q

what is a genome

A

the entire set of genetic material in an organism

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24
Q

how has the identification of the entire human genome helped scientists

A

able to identify the specific genes that are linked to specific diseases and chose more affective treatments/ create more affective treatments

  • also helped us be able to track our ancestors
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25
Q

what is an allies

A

a different forms of the same gene

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26
Q

what is the difference between homozygous and heterozygous

A

we have two copies of every gene (one from mother and one from father) meaning we have two allies of each gene. these can be the same allies (homo) or different allies (hetro)

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27
Q

what are dominant and recessive allies

A

when there are two different allies (hetro), they will either be dominant or recessive. the dominant allies will take dominance over the characteristic and that one will always be expressed. the only way for the recessive allies to be expressed is if both allies are recessive

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28
Q

what is genotype and phenotype

A

genotype - the collection of allies we have
(dominant/recessive etc)
phenotype - the characteristics we receive from the genotype

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29
Q

what is an inherited disorder

A

group of conditions that can be passed on in allies and can be inherited from parents

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30
Q

what are two examples of an inherited disorder

A

polydactyly and cystic fibrosis

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31
Q

explain the inherited disorder of “polydactyly”

A

when a baby is born with extra fingers or toes.
it is caused by a dominant allele

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32
Q

explain the inherited disorder of “cystic fibrosis”

A

it is caused by a recessive allele
it is a disorder of cell membranes which causes thick sticky mucus in different parts of the body - lungs and pancreas

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33
Q

what is embryo screening

A

when having an IVF, scientists will take a cell from the embryo to look at the genes and investigate weather they are carrying any genetic disorders

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34
Q

what are the pros and cons of embryonic screening

A
  • reduce overall suffering as fewer people will suffer from health problems
  • save a lot of money - treating disorders are expensive
  • implies people with genetic disorders are less desirable
  • future screening for other traits
35
Q

what is variation

A

any difference between the individuals phenotype in a species or groups of organisms of any species

36
Q

what is variation dependant on

A

genes and proteins yet also your environment

37
Q

what is a mutation

A

change in the DNA code so that the protein it codes for may be different. most don’t have an effect on the protein and therefore don’t change the organisms phenotype

38
Q

what is the survival of the fittest

A

some mutations are beneficial giving individual good characteristics which were being passed down to their offspring therefore more likely to survive

39
Q

what is natural selection

A

individuals that are less adapted to the environment are less likely to survive

40
Q

what is evolution

A

the development of any organism over a period of time in order to adapt and survive in their changing environment. this could lead to a change in the whole species or even a development of a new species

41
Q

what is selective breeding

A

when you breed the best plant or animals in the population to create the best offspring and best allies for the best traits

42
Q

how do we selective breed

A

select the best two in your population and breed them together over and over always picking the best offspring

43
Q

what is the negatives of selective breeding

A
  • reduces the gene pool of the population
  • lead to inbreeding making offspring prone to diseases or inherited defects
  • less variation therefore a pathogen could infect all plants at once
44
Q

what is a gene pool

A

collection of different allies in a population and because we select the allies with the most wanted characteristics we are left with a smaller pool of allies

45
Q

what is genetic engineering

A

modification of an organisms’ genome by inserting a gene from another species

46
Q

what are two examples of genetic engineering we have completed to help in the medication industry

A

genetically modified sheep to produce a specific drug in their milk
genetically modified bacteria to produce the human hormone insulin to treat diabetes

47
Q

how are we currently trying to use genetic engineering to cure inherited disorders (caused by faulty genes) and why is it proving difficult)

A

gene therapy - giving the person a healthy version of the gene

difficult - the faulty gene is in all the cells and therefore is difficult to transfer the new gene to every cell in the body - transfer at an early stage of development

48
Q

pros and cons of genetically modified (engineered) crops

A

pros - easliy make crops have desireab characteristics - more fruit, resist diseases - more food for less money - important in developing counterues
- produce special nutrience

cons - we dont know exactly how genetically modified plants effect human health
- could make their way into the wild and effect the whole ecosystem

49
Q

during genetic engineering, how is the gene transferred from one organism to another

A
  • find the gene we want and cut section of DNA - “isolate it” using enzymes
  • insert gene into a vector - virus or a bacterial plasmid
  • introduce the vector to the organism which will then take in the vector and gene and begin to produce the protein the gene codes for
50
Q

what is bacterial plasmid

A

little loops of DNA that bacteria hold

51
Q

what are the two ways plants can be cloned

A

take cuttings, tissue culture

52
Q

what is the main advantage of cloning plants

A

because it is genetically identical to the original plant we know exactly what characteristics the clone is going to have

53
Q

how is plant cloning completed using the method of taking cuttings

A

a small piece of a plant is removed and the end is dipped in rooting powder which contains plant hormones encouraging the plant to grow and develop roots

54
Q

how is plant cloning completed using the method of tissue culture

A

take the plant we want to clone and divide it into hundreds of tiny pieces, these small groups of cells are incubated with plant hormones, stimulating them to grow and develop. need sterile conditions

55
Q

what are the benefits of using tissue culture to develop clones of plants

A

allows growers to produce hundreds of clones quickly and cheaply
to preserve rare species of plants

56
Q

what are the two ways of cloning animals

A

embryo transfer, adult cell cloning

57
Q

how is animal cloning completed using the method of embryo transfer

A

-start with sperm and egg cell from the mammal with desired characteristics
-fertilisation produces a fertilised egg which is then developed into an early stage embryo - not had a chance to specialise
-use a glass rod to split embryo into two
- transplant the two embryos into host mothers

58
Q

how is animal cloning completed using the method of adult cell cloning

A

-remove a cell from the mammal and remove the nucleus which contains the genetic information
- take an unfertilised egg cell and remove the nucleus and replace with nucleus from other mammal
- give egg cell an electric shock to divide it and form embryo
-inserted into host mother

59
Q

what is the benefit of adult cell cloning

A

we know the characteristics that the clone will have

60
Q

what is Darwin’s theory of evolution

A

evolution occurred by natural selection

61
Q

why wasn’t Darwin’s theory accepted and controversial

A

at the time people heavily believed in God and his creation of the world, Darwin’s theory went against this. scientists at the time also felt like there wasn’t enough evidence and people didn’t understand how characteristics were inherited

62
Q

what did Jean Lamarck suggest

A

that when a characteristic is regularly used it becomes more developed and passed onto offspring

63
Q

what is speciation

A

the process of how new species form

64
Q

Who is Alfred Wallace and what did he want to know/ what did he find out

A

wanted to know how warning colours on animals evolved
- found out the theory of evolution by natural selection and him and Darwin put their theories together

65
Q

what do you need in order for speciation to occur

A

a geographical barrier

66
Q

explain the process of speciation

A
  • if a species of an organism are on an island they are interbreeding spreading beneficial mutation
  • if the species get separated by a geographical barrier there will no longer be interbreeding between two groups
  • over time, natural selection will favour different allies on both sides meaning over generations the populations phenotypes will change
67
Q

how did Mendel study inheritance

A

through carrying out breeding experiments of plants and analysing the ratios of characteristics in offspring

68
Q

why was Mendel’s work not recognised until after his death

A

he couldn’t explain the mechanisms of inheritance as chromosomes were not discovered

69
Q

what are the two types of evidence to support the theory of evolution

A

fossils and antibiotic resistant bacteria

70
Q

what are fossils

A

the remains of organisms from millions of years ago which are found in rocks

71
Q

what are the three ways in which fossils are formed

A
  1. parts of an organism that hasn’t decayed - if the conditions for decay weren’t present
  2. parts of the organism were slowly replaced by minerals in the decay process
  3. can be preserved traces of organisms like footprints
72
Q

what are the problems with fossils

A

many early forms of life had soft bodies with little to no bones

73
Q

what are the reasons for a species to go extinct

A

catastrophic event
changing weather patterns
new predator or disease
new more successful species evolved

74
Q

how do fossils provide evidence for evolution

A

scientist can identify the age of fossils and use them to show the development over time

75
Q

give an example of a resistant bacteria

76
Q

why does bacteria evolve quickly

A

because of their fast rate of reproduction

77
Q

how does antibiotic resistence occur

A
  • mutations occur in bacteria producing genetic variations
  • certain strains of bacteria resistant to bacteria are not killed when antibiotic applied
  • resistant strains survive and reproduce
  • over time the population of resistant strain increases
78
Q

how can we reduce the amount of antibiotic resistant bacteria

A
  • only prescribe antibiotics when necessary
  • completing the full course of antibiotics
  • reduce the amount of antibiotics used in farming
79
Q

what is the classification system created by Linnaeus

A

kingdoms, phylum, class, order, family, genus, species

80
Q

how are organisms classified

A

their characteristics and structure

81
Q

how do you name a species according to the binomial system

A

genus name followed by species name

82
Q

why were new classification models developed

A

development in microscopy - better examination of organisms internal structures
improvement in understanding biochemical processes - such as DNA

83
Q

what are the three domains and what are they

A

archaea - bacteria living in extreme conditions
bacteria - like inside body
eukarya - plants, animals, fungi, protist

84
Q

how are evolutionary trees created

A

examine the DNA of different species and analyse how similar they are