variation and selection Flashcards
Variation is defined as
differences between individuals of the same species
Phenotypic variation is
the difference in features between individuals of the same species
Phenotypic variation is the difference in features between individuals of the same species
Some of these differences are caused by differences in genes, which is
genetic variation
Phenotypic variation can be divided into two types depending on…: …
- how you are able to group the measurements:
Continuous Variation is when there are very many small degrees of difference for a particular characteristic between individuals and they are arranged in order
Examples include height, mass, finger length etc. where there can be many ‘inbetween’ groups
Discontinuous Variation is when there are distinct differences for a characteristic
For example, people are either blood group A, B, AB or O; are either male or female; can either roll their tongue or not – there are no ‘inbetweens’
When graphs of Continuous Variation are plotted, they give … (a result of all the small degrees of difference), whereas discontinuos variation …
-smooth bell curves
-gives a step-like shape
is it a type of …variation

height is an example of continuous variation which gives rise to a smooth bell-shaped curve when plotted as a graph
what type of variation

Blood group is an example of discontinuous variation which gives rise to a step-shaped graph
Phenotypic variation can be caused in two main ways:
It can be genetic – controlled entirely by genes
Or it can be environmental – caused entirely by the environment in which the organism lives
Examples of genetic variation in humans include:
blood group
eye colour
gender
ability to roll tongue
whether ear lobes are free or fixed:
Environmental Variation
Characteristics of all species can be affected by environmental factors such as climate, diet, accidents, culture, lifestyle and accidents during lifetime
In this instance ‘environmental’ simply means ‘outside of the organism’
Examples include:
An accident may lead to scarring on the body
Eating too much and not leading an active lifestyle will cause weight gain
Being raised in a certain country will cause you to speak a certain language with a certain accent
A plant in the shade of a big tree will grow taller to reach more light
Genetic and Environmental Causes
Discontinuous variation is usually caused by genetic variation alone
Continuous features often vary because of a combination of genetic and environmental causes, for example:
tall parents will pass genes to their children for height
their children have the genetic potential to also be tall
however if their diet is poor then they will not grow very well
therefore their environment also has an impact on their height
Another way of looking at this is that although genes decide what characteristics we inherit, the surrounding environment will affect how these inherited characteristics develop
Mutations are
random genetic changes
Most mutations have no effect
on the phenotype as the protein that a mutated gene produces may work just as well as the protein from the non-mutated gene
Rarely, mutations lead to the development of new alleles and so new phenotypes and if they do, most have a small effect on the organism
Occasionally, the new allele gives the individual a … over other members of the species
for example:…
Mutations can also lead tos that can have dramatic effects on the body…for example:…
Mutations happen… and .. but their frequency can be …by exposure to the following: …
Increased rates of mutation can cause cells to become …, which is why the above are linked to increased incidence of different types of
- survival advantage
- A bird develops a mutation leading to a change in feather colours
This makes it more attractive to birds of the opposite sex
Which causes the bird to breed more frequently and have more chances of passing on the mutated phenotype to the next generation
- harmful change
- sickle cell anaemia in humans
- spontaneously
- continuously
- increased
-
Gamma rays, x – rays and ultraviolet rays – all types of ionising radiation which can damage bonds and cause changes in base sequences
Certain types of chemicals – for example chemicals such as tar in tobacco
- cancerous
- cancer
Sickle Cell Anaemia
Sickle cell anaemia was the first genetic disease to be described in terms of a gene mutation
A gene mutation is a change in the base sequence of DNA
The mutation changes the molecule haemoglobin, causing the red blood cells (RBC’s) to become stiff and sometimes sickle-shaped when they release oxygen to the body tissues
The sickled cells tend to get stuck in narrow blood vessels, blocking the flow of blood
As a result, those with sickle cell disease suffer painful “crises” in their joints and bones
They may suffer strokes, blindness, or damage to the lungs, kidneys, or heart. They must often be hospitalized for blood transfusions and are at risk for a life-threatening complication called acute chest syndrome
Although many sufferers of sickle cell disease die before the age of 20, modern medical treatments can sometimes prolong these individuals’ lives into their 40s and 50s

Inheritance of sickle cell
There are two versions or alleles of the gene important for the inheritance of sickle cell anaemia : A and S
The two alleles are codominant, meaning there is no ‘dominant’ or ‘recessive’ version of the gene
Individuals with two A alleles (HbAHbA) have normal haemoglobin, and therefore normal RBCs
Those with two S alleles (HbSHbS) develop sickle cell anaemia
Those who are heterozygous for sickle cell (HbAHbS) produce both normal and abnormal haemoglobin (as the alleles are codominant)
Heterozygous individuals are usually healthy, but they may suffer some symptoms of sickle cell anaemia under conditions of low blood oxygen, such as high altitudes or during exercise
Heterozygous individuals are said to be ‘carriers’ of the sickle cell gene and are said to have ‘sickle cell trait’
Inheritance of sickle cell trait: (punnett square)

Inheritance of sickle cell disease:(disease)

Sickle cell anaemia & natural selection
In the United States, about 1 in 500 African-Americans develops sickle cell anaemia
In Africa, about 1 in 100 individuals develops the disease
Why is the frequency of such a serious disease so much higher in Africa? The answer is to do with malaria
Malaria is a disease spread by mosquitoes that are endemic in many areas of Africa and causes over 1 million deaths per year
In the late 1940s, studies of diseases in populations suggested a connection between African populations, malaria and sickle cell disease
A theory was suggested; if the heterozygous individuals (HbAHbS) are protected from malaria, and the negative effects (of sickle cell) are only present in the small proportion of people who are homozygous for the affected allele (HbSHbS), then the affected allele could become more common
Later studies supported this theory, showing that African children who are heterozygous for the sickle cell allele have a ten-fold reduction in their risk of getting malaria
This means that there is a strong correlation between the prevalence of sickle cell anaemia in areas of the world where malaria is common

You should be able to explain how these maps support the idea that having…
You should also be able to use numerical data and graphs given in exam questions to explain this.
a sickle cell allele gives resistance to malaria.




