Diversity, Variation And Classification Flashcards
What is Meiosis?
β’ A type of cell division where gametes
are made
β’
β’ Gametes are haploid (Contain only 1of each chromosome).
> allows them to come together in
reproduction to form a diploid cell
(has a pair/2 of each chromosome)
How can you compare meiosis and mitosis
Mitosis
- chromosome number remains same
- cells produced are diploid
- produced identical only
- one division/2 cells produced
- body cell formation
Meiosis
- chromosome number halved
- cells produced haploid
- cells produced not identical
- two divisions /4 cells produced
- used in gamete formation
..
Theyβre different as
- mitosis only involves one division (wch separates sister chromatids)
- meiosis has two divisions (wch separate homologous pairs then sister chromatids).
-
- Thereβs no pairing or separating of homologous chromosomes in mitosis
- and so no crossing over or independent segregation of chromosomes.
So produces genetically identical daughter cells β unlike meiosis.
How is DNA from One Generation is Passed to the Next by Gametes
1) Gametes are the sperm cells in males and egg cells in females.
> join together at fertilisation to form a zygote, wch divides and develops into a new organism.
2) Normal body cells have the diploid number (2n) of chromosomes
β meaning each cell contains two of each chromosome,
one from mum and one from dad.
3) Gametes have a haploid (n) number of chromosomes - only one copy of each chromosome.
4) At fertilisation, a haploid sperm fuses with a haploid egg,
making cell with normal diploid number of chromosomes.
> Half these chromosomes are from sperm and half are from egg
During sexual reproduction, any sperm can fertilise any egg β fertilisation is random.
- Random fertilisation produces zygotes with diff combos of chromosomes to both parents.
- This mixing of genetic material in sexual reproduction increases genetic diversity in a species
(2n/n is another way to represent diploid/haploid)
How Gametes are Formed by Meiosis, and what meiosis is
Meiosis is a type of cell division.
> takes place in the reproductive organs.
> Cells that divide by meiosis start diploid, but cells formed from meiosis are haploid
β
β the chromosome number halves. Without meiosis, youβd get double the number of chromosomes when gametes fuse.
1) Before meiosis, DNA unravels and replicates
> so are two copies of each chromosome/two chromatids.
2) DNA condenses to double-armed chromosomes,each made w two sister chromatids, joined by centromere.
3) Meiosis I (first division) - the chromosomes arrange themselves into homologous pairs.
4) These homologous pairs then separate, halving chromosome number.
5) Meiosis Il (2nd division) - pairs of sister chromatids wch make each chromosome separate (centromere divides).
6) Four haploid cells (gametes) that are genetically different are produced.
diagram 1
..
About Homologous Pairs..
- Humans have 46 chromosomes β 23 pairs. One in each pair came from mum and one from dad,
> e.g. two number lβs (one from mum and one from dad), two number 2βs etc.
-
- The chromosomes that make up each pair are same size and same genes
- but may have diff gene versions (alleles).
- These pairs of chromosomes are called homologous pairs
What happens when Chromatids Cross Over in Meiosis 1
During meiosis 1, homologous pairs of chromosomes come together and pair up. - The chromatids twist round each other and bits of chromatids swap over.
The chromatids still contain the same genes but
now have a diff combination of alleles.
diagram 2
In what 2 events does Meiosis allow Production of Cells that are Genetically Different
There are two main events during meiosis that lead to genetic variation:
1) Crossing over of chromatids
- crossing over of chromatids in meiosis I
means that each of four daughter cells formed in meiosis contains chromatids with diff alleles
-
- after crossing over, one chromosome from each homologous pair ends up in each cell
- each cell has a different chromatid, so a diff allele set, increasing genetic variation
..
2) Independent segregation of chromosomes
- Each homologous pair of chromosomes in cells is made up of one chromosome
- from mum and one from dad
-
- When homologous pairs are separated in meiosis 1, itβs random wch chromosome ends up in wch daughter cell.
- four daughter cells produced have diff combos of maternal/paternal chromosomes.
> One chromosome from each homologous pair ends up in each cell.
This is independent segregation of the chromosomes.
- Each cell has a diff chromatid and so a diff set of alleles, wch increases genetic variation in potential offspring
Chromosome Mutations and what are they caused by
Chromosome Mutations
- caused by Errors in Cell Division
In humans, when meiosis works properly, all four daughter cells end up with
23 whole chromosomes
- one from each homologous pair (1 to 23), but arent homologous pairs
But can go wrong; cells produced contain
- variations in numbers of whole chromosomes
- or parts of chromosomes.
1) eg, two cells from meiosis may have 23 whole chromosomes,
- one each of 1 to 23, but the other two may have two chromosome 6βs and other, no chromosome 6.
2) This is chromosome mutation and is caused by errors during meiosis.
3) Chromosome mutations lead to inherited conditions as errors are present in gametes (hereditary cells).
- One type of chromosome mutation is called non-disjunction
β a failure of chromosomes to separate properly.
βIn ppl, non-disjunction of chromosome 21 in meiosis leads to Downβs Syndrome.
What is non disjunction in chromosome mutation and how does it lead to downs syndrome
Downβs syndrome is caused by one having an extra copy of chromosome 21
(or sometimes an extra copy of part of chromosome 21).
>
»_space; Non-disjunction in this case is where chromosome 21 fails to separate properly
»_space; in meiosis, so one cell gets an extra copy of 21 and another gets none.
>
Β» Non-disjunction occurs (failure of chromosomes to separate properly)
- homologous pair fails to separate.
When gamete with extra copy fuses to another gamete at fertilisation, - the resulting zygote will have three copies of chromosome 21.
What are mutations and the types
Gene mutations involve a change in DNA base sequence of chromosomes.
The types of errors that can occur include:
- Substitution β one base is substituted with another
-> e.g. ATGCCT becomes ATTCCT.
- Deletion β one base is deleted
-> e.g. ATGCCT becomes ATCCT.
-
- Errors can also be caused by
- insertion, duplication, addition and translocation of bases.
the order of DNA bases in a gene determines order of amino acids in a particular protein.
- If a mutation occurs in a gene
- the sequence of amino acids it codes for (and the protein formed) cd be altered
How do Not All Mutations Affect the Order of Amino Acids
The degenerate nature of the genetic code
- means some aas are coded for by more than one DNA triplet.
- so not all substitutions will result in a change to amino acid sequence of protein
β coding for the same aa
HOWEVER deletions will
β the deletion of a base will change number of bases present, wch will
cause a shift in all base triplets after it.
What are Mutagenic Agents
Mutations occur spontaneously
- e.g. when DNA is misread during replication.
But some things cause an increase in rate of mutations
β these are called mutagenic agents.
- Ultraviolet radiation
- ionising radiation
- some chemicals
- some viruses
What do Lots of Different Alleles Mean in terms of a High Genetic Diversity
Genetic diversity describes the number of alleles in a species or population,
- and natural selection increases proportion of advantageous alleles.
- Itβs all abt the most well-adapted organisms getting on with some reproduction.
1) Remember, there can be diff versions of a single gene β alleles
2) Genetic diversity is number of diff alleles of genes in a species or population.
3) Genetic diversity within a population is increased by:
- Mutations in DNA - forming new alleles.
- Diff alleles being introduced into a population when individuals from another population migrate into them and reproduce. This is known as gene flow.
> A population is a group of organisms of one species living in a particular habitat.
Genetic diversity is what allows natural selection to occur
What are Genetic Bottlenecks
A genetic bottleneck is an event that causes
- a big reduction in a population
- e.g. when a large number of organisms in a population die before reproducing.
This reduces the number of diff alleles in gene pool so reduces genetic diversity.
> The gene pool is the complete range of alleles in a population.
The survivors reproduce
> a larger population is created from a few individuals.
What is The Founder Effect (a Type of Genetic Bottleneck)
The founder effect describes what happens
- when a few organisms from a population start a new colony
- where there are a small number of diff alleles in initial gene pool.
- frequency of each allele in new colony may be very diff to frequency
- of those alleles in original population
β
β eg, an allele rare in original population may be more common in new. - may lead to a higher incidence of genetic disease.
The founder effect can occur as a result of migration, leading to geographical separation
- or if a new colony is separated from original population for another reason, such as religion.
»_space; eg the amish in USA
How does Natural Selection Increase Advantageous Alleles in a Population
Randomly-occurring mutations sometimes result in a new allele being formed.
- can be harmful. wch usually means the mutated allele quickly dies out.
However, some mutations can produce alleles that are beneficial to an organism
> (e.g. a protein is produced that works better than original)
> helping organism survive in certain environments.
>
> When allele codes for characteristic that increases chances of survival,
> its frequency in the population can increase.
This process is known as natural selection. Hereβs how it works:
1) Not all organisms are as likely to reproduce as each other.
- Thereβs differential reproductive success in a population
- ones with allele that increases chance of survival are more likely to survive, reproduce and pass genes (including the beneficial allele),
- than individuals with diff alleles
2)means that a greater proportion of next generation inherits beneficial allele.
3)so they are more likely to survive, reproduce and pass their genes.
4) So the frequency of beneficial allele increases from generation to generation.
5) Over generations this leads to evolution as advantageous alleles become more common in population.
Adaptation and selection are both key factors in evolution
- the gradual change in species over time.
- Evolution has led to huge diversity of living organisms on Earth.
How does Natural Selection Lead to Populations Becoming Better Adapted
Adaptations help organisms to survive in their environment.
- They can be behavioural, physiological or anatomical.
Here are some examples:
1) Behavioural adaptations
> Ways an organism acts that increase chance of survival and reproduction.
»_space; eg, possums βplay deadβ if threatened by a predator to escape attack.
2) Physiological adaptations
> Processes inside an organismβs body that increase chance of survival.
»_space; eg, brown bears hibernate over winter.
- They lower rate of metabolism (all the chemical reactions taking place in their body).
- This conserves energy, so donβt need to look for food in months when scarce.
3) Anatomical adaptations
> Structural features of an organismβs body that increase chance of survival.
»_space; eg. whales have a thick layer of blubber (fat) wch helps keep warm in cold sea.
How may Different Types of Natural Selection Lead to Different Frequency Patterns
You might remember natural selection alters allele trequency in a population.
- stabilising and directional selection are types of natural selection that affect allele freq in diff ways..
β’ Antibiotic Resistance Shows Directional Selection
- Directional selection is where individuals with alleles for characteristics of an extreme type are more likely to survive/reproduce
- cd be in response to an environmental change
>
> Bacteria evolving antibiotic resistance is an example
β’ Human Birth Weight Shows Stabilising Selection
- Stabilising selection is where individuals with alleles for characteristics towards middle of range are more likely to survive and reproduce.
- occurs when environment isnβt changing,
- reduces range of possible characteristics.
>
> An example of stabilising selection is human birth weight.
How does directional selection work in antibiotic resistance
1) Some individuals in a population
have alleles that give resistance to an antibiotic.
2) The population is exposed to antibiotic, killing bacteria without resistant allele.
3) The resistant bacteria survive and reproduce without competition,
passing on
the allele that gives antibiotic resistance to their offspring.
4) After some time, most organisms in the population will carry the antibiotic resistance allele.
How does stabilising selection work in terms of human birth rates
1) Humans have a range of birth weights.
2) Very small babies are less likely to survive
β partly as they find it hard to maintain their body temperature.
3) Giving birth to large babies can be difficult, so large babies are less likely to survive too.
4) Conditions are most favourable for medium-sized babies
- so weight of human babies tends to shift towards middle of the range.
How do you interpret data on effects of effects of selection
1) describe what data shows (type of natural selection, and how number show that)
2) say why (more likely to survive winter eg and reproduce)
How Can you Investigate Effects of Antibiotics on Bacterial Growth
You Test the Effects of Antibiotics Using Agar Plates
1) The bacteria youll use are likely to have been grown
- in a liquid broth (mixture of distilled water, bacterial culture and nutrients).
2) Use sterile pipette to transfer bacteria from broth
- to an agar plate (petri dish with agar jelly.)
- Spread bacteria over plate using sterile plastic spreader.
3) Use sterile forceps to place paper discs soaked
- with diff antibiotics spaced apart on plate.
- Make sure you add negative control disc soaked only in sterile water.
4) Lightly tape lid on, invert, incubate plate
- at about 25 Β°C for 48 hours. This allows the bacteria to grow (forming βlawnβ).
- Anywhere bacteria canβt grow can be seen as clear patch in lawn of bacteria.
»_space; This is called an inhibition zone.
5) The size of an inhibition zone tells you how well an antibiotic works.
- larger the zone, the more the bacteria were inhibited from growing.
6) A similar technique can be used to test effects of antiseptics or disinfectants on microbial growth.
diagram 3 for result
What are Aseptic Techniques to Prevent Contamination of Microbial Cultures
Aseptic techniques prevent contamination of cultures by unwanted microorganisms.
> important as contamination can affect growth of microorganism that youβre working with.
>
> also important to avoid contamination with disease-causing microbes that could make you ill.
When carrying out antibiotic investigation, use following aseptic techniques:
1) Regularly disinfect work surfaces to minimise contamination.
- Donβt put any utensils on work surface.
- Contaminated utensils should be placed in beaker of disinfectant.
2) Use sterile equipment and discard safely after use.
- E.g. glassware can be sterilised before and after use in an autoclave
- steams equipment at high pressure
- Pre-sterilised plastics instruments are used once, then discarded.
3) Work near Bunsen flame.
- Hot air rises, so any microbes in air shd be drawn away from culture.
4) Minimise time spent with lid off agar plate,
- reduces chance of airborne microorganisms contaminating culture.
5) Briefly flame neck of glass container of broth just after opened/just before closed β causes air to move out container, preventing unwanted organisms from falling in.
6) You shd also take steps to protect yourself,
- e.g. wash hands thoroughly before and after handling cultures.
Phylogeny Tells Us What About the Evolutionary History of Organisms
Phylogeny is the study of evolutionary history of groups of organisms.
- tells us whoβs related to whom and how closely related they are.
-
- All organisms have evolved from shared common ancestors (relatives).
> can be shown on a phylogenetic tree
diagram 4
This tree show relationship between members of Hominidae family (great apes and humans).
- The first branch point represents a common ancestor of all family members.
> This ancestor is now extinct.
- Orangutans were the first group to diverge (evolve to be a diff species) from this common ancestor.
- Each of following branch points represents another common ancestor
- from wch a diff group diverged. Gorillas diverged next, then humans, then bonobos and chimpanzees.
- Closely related species diverged away from each other most recently.
- E.g. humans and chimpanzees are closely related, as diverged recently.
- You can see this as their branches are close together.
How is Classification All About Grouping Together Related Organisms
Taxonomy is the science of classification.
> involves naming organisms and organising them into groups.
> makes it easier to identify and study them.
-
- Scientists now take into account phylogeny when classifying organisms
- and group organisms according to their evolutionary relationships.
1) There are eight levels of groups used to classity organisms.
- These groups are called taxa.
- Each group is called a taxon.
2) The groups are arranged in a hierarchy,
- with largest groups at top
- smallest groups at the bottom
- Organisms can only belong to one group at each level in hierarchy β thereβs no overlap.
3) Organisms are first sorted into three large taxa called domains
β the Eukarya, Bacteria and Archaea.
4) Related organisms in a domain are then sorted to smaller groups called kingdoms, > e.g. all animals are in animal kingdom.
- domain
- kingdom
- phylum
- class
- order
- family
- genus
- species
5) As you move down hierarchy,
> more groups at each level
> but fewer organisms in each group.
The organisms in each group also become more closely related
6) in the final group - species
β the groups there contain only one type of organism (e.g. humans, dogs, E. coli).
7) Scientists constantly update classification systems
- as of discoveries abt new species and new evidence abt known organisms
- (e.g. DNA sequence data)