Biodiversity, Evolution and Disease

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What diseases are caused by bacteria? What are the symptoms, and how are they transmitted, treated and prevented?

Tuberculosis infects the lungs

  • Coughing blood, weight loss, high temperature

  • Airborne

  • Treated by antibiotics

  • Prevented by vaccinations

Meningitis inflammes the tissue surrounding the brain and spinal cord (meninges)

  • High temperature, headache, rash, neck stiffness

  • Transmitted through contact and the air

  • Treated by antibiotics

  • Prevented by vaccinations

Ring rot infects potato and tomato plants

  • Wilting, discolouration, vascular tissue rots and turns black

  • Transmitted through contact

  • No cure

  • Prevented by using clean equipment and destroying infected plants

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What diseases are caused by fungi? What are the symptoms, and how are they transmitted, treated and prevented?

Black sigatoka affects banana plant leaves

  • Black/brown streaks and leaf death

  • Transmitted by spores and through rain splashes

  • Treated by fungicides

  • Prevented by fungicides, keeping space between trees and removing affected leaves

Ringworm infects cattle

  • Grey ring shaped rashes

  • Transmitted through contact

  • Treated by anti-fungal creams

  • Prevented by reducing overcrowding

Athlete’s foot affects feet in humans

  • Cracking and scaling, itchy skin between toes

  • Transmitted by contact

  • Treated by anti-fungal creams

  • Prevented by keeping feet clean and dry, avoiding public showers and swimming pools

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What diseases are caused by protoctists? What are the symptoms, and how are they transmitted, treated and prevented?

Malaria damages the red blood cells, liver and brain

  • Nausea, vomiting, fever, chills, headache, fatigue

  • Transmitted by anopheles mosquito vectors

  • Treated by antimalarial medicine

  • Prevented by antimalarial medicines, insect repellents, mosquito nets and avoiding stagnant water

Potato blight is a fungus-like protoctist that damages potato and tomato crops

  • Small, brown rotting spots on leaves, decaying tubers

  • Transmitted by spores

  • No cure

  • Prevented by removing infected plants, using resistant strains and fungicides

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What diseases are caused by viruses? What are the symptoms, and how are they transmitted, treated and prevented?

Tobacco mosaic virus damages many plant species

  • Stunted growth, yellow mosaic patterns on leaves

  • Transmitted by contact

  • No cure

  • Prevented by removing infected plants, using resistant varieties and disinfecting tools

Influenza A, B and C damage ciliated epithelial cells

  • High temperatures, coughing, headache, fatigue

  • Transmitted by airborne droplets that can stay on surfaces

  • Treated by antiviral drugs and rest

  • Prevented by vaccines and good hygiene

HIV is a virus that damages the immune system and can lead to AIDS

  • Flu-like symptoms that disappear

  • Transmitted through bodily fluids

  • No cure but can be treated by antiretroviral medicines

  • Prevented by using condoms, abstinance, not sharing needles, post and pre-exposure medicines

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What are the two types of disease transmission?

  • Direct - from one host to another host

  • Indirect -  a second organism (vector) that is unaffected by the pathogen transfers it to a new host

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What are the methods of direct disease transmission?

  • Contact- skin-skin or contact with bodily fluids

  • Inoculation- through a wound

  • Droplets- infected droplets come into contact with a person

  • Fungal spores- travel through the air

  • Vertical transmission- from mother to baby during pregnancy

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What are the methods of indirect disease transmission?

  • Vectors- an infected host (ie. insect) carries disease from one organism to another

  • Airborne- infected droplets are inhaled after being suspended in the air

  • Fomites- inanimate objects carrying diseases

  • Food and waterborne- ingestions of contaminated food and water

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What factors can affect disease transmission in animals?

  • Overcrowding (close proximity)

  • Poor nutrition

  • Compromised immune system (HIV/AIDs/taking immunosuppressants)

  • Poor waste disposal

  • Climate change (certain animal vectors prefer different climates)

  • Lack of public awareness/doctors

  • Migration

  • Certain unsanitary cultural traditions

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What factors can affect disease transmission in plants?

  • Overcrowding (density of planting)

  • Disease resistance

  • Poor soil nutrition

  • Climate change

  • Wind strength

  • Farming practices

  • Water/soil contamination

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What non-specific passive physical defences are present in plants?

  • Waxy cuticle on leaves

  • Cellulose cell walls

  • Lignified bark

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How do plants detect pathogen attack?

  • Receptors in the cell membrane recognise molecules from the pathogen and chemicals produced by attack of the cell wall

  • Signalling molecules switch on genes in the nucleus

  • This triggers the production of defensive chemicals, substances to act as physical barries, and signals to trigger the defences of nearby cells

<ul><li><p>Receptors in the cell membrane recognise molecules from the pathogen and chemicals produced by attack of the cell wall</p></li><li><p>Signalling molecules switch on genes in the nucleus</p></li><li><p>This triggers the production of defensive chemicals, substances to act as physical barries, and signals to trigger the defences of nearby cells</p></li></ul>
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What physical defenses can be triggered in plants due to attack?

  • Callose, a polysaccharide of beta glucose monomers, is produced, which is deposited between cell walls, sieve tube pores, and in the plasmodesmata connecting cells, and blocks further spread of the pathogen to other cells and parts of the plant

  • Lignin is added to cell walls to strengthen and thicken them

  • Stomata can be closed to prevent further attack

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What chemical defenses can be triggered in plants due to attack?

  • Insect repellants eg. pine resin and citronella

  • Insectides eg. pyrethrins (neurotoxin in chrysanthemums) and caffeine

  • Antibacterial compounds eg. phenols, gossypol (in cotton), defensins and lysosomes

  • Antifungal compounds eg. phenols, gossypol, caffeine, saponins and chitinases (break down fungal cell walls)

  • Toxins eg. cyanide

Often we extract these substances, as they are useful to us for pathogen defence, as well as herbs and spices

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Why are plants unique in their pathogen response?

Oftentimes plants don’t try to heal tissues damaged by disease, they just section it off and sacrifice it (leaf drop/necrosis/abscission)

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What non-specific defenses are present in animals?

  • Skin

  • Mucous membranes lining gas exchange surfaces

  • Chemical defenses (stomach acid + lysosomes in tears and urine)

  • Blood clotting + wound repair

  • Inflammation

  • Expulsive reflexes (coughing, sneezing and vomiting)

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How does the skin defend against pathogens?

  • Physical barrier

  • Secretes sebum, which inhibits pathogen growth

  • Has a natural population of bacteria that out-compete pathogens

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How do mucous membranes defend against pathogens?

  • Goblet cells secrete mucus (containing lysosomes) that traps + destroys pathogens

  • Cilia waft pathogens towards the throat to be coughed out

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How do blood clotting + wound repair defend against pathogens?

  • Platelets at a wound release thromboplastin and serotonin

  • Thromboplastin triggers a clotting reaction cascade

  • This causes the soluble protein fibrinogen to be converted to insoluble fibrin, forming a scab

  • Serotonin reduces the supply of blood to the area

  • The scab formed acts as a physical barrier while epidermal cells grow underneath and collagen reinforces the skin

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How does inflammation defend against pathogens?

  • Mast cells release histamines and cytokines

  • Histamines dilate the blood vessels (causing redness and heat that prevents pathogens reproducing) and increase membrane permeability (causing tissue fluid to escape resulting in swelling and pain)

  • Cytokines attract phagocytes to the site to destroy pathogens (eg. interleukins)

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What are the types of white blood cells and what do they do?

Phagocytes- non-specific immune response of engulfing pathogens, by phagocytosis (includes neutrophils and macrophages)

Lymphocytes- specific immune response of producing antibodies, killing pathogens and regulating of the immune response (includes T and B lymphocytes)

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What is the process of phagocytosis by neutrophils?

  • Neutrophils recognise an antigen from a pathogen as being foreign or ‘non-self’

  • They engulf the pathogen in a vacuole, to form a phagosome

  • Lysosomes bind to the phagosome to form a lysophagosome

  • The enzymes in the lysosomes break down the pathogen

  • The products of this are removed from the cell by exocytosis

<ul><li><p>Neutrophils recognise an <strong>antigen</strong> from a pathogen as being <strong>foreign </strong>or ‘non-self’</p></li><li><p>They <strong>engulf</strong> the pathogen in a <strong>vacuole</strong>, to form a <strong>phagosome</strong></p></li><li><p><strong>Lysosomes </strong>bind to the phagosome to form a <strong>lysophagosome</strong></p></li><li><p>The enzymes in the lysosomes break down the pathogen</p></li><li><p>The products of this are removed from the cell by <strong>exocytosis</strong></p></li></ul>
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What is the process of phagocytosis by macrophages?

  1. Macrophages recognise an antigen from a pathogen as being foreign or ‘non-self’

  2. They engulf the pathogen in a vacuole, to form a phagosome

  3. Lysosomes bind to the phagosome to form a lysophagosome

  4. The enzymes in the lysosomes break down the pathogen

  5. The products of this bind to the antigens from the macrophage, to form a major histocompatibility complex (MHC) in the cytoplasm

  6. The macrophage then displays these antigens on the cell membrane to become an antigen-presenting cell, which will stimulate lymphocytes in the specific immune response

<ol><li><p>Macrophages recognise an <strong>antigen</strong> from a pathogen as being <strong>foreign </strong>or ‘non-self’</p></li><li><p>They <strong>engulf</strong> the pathogen in a <strong>vacuole</strong>, to form a <strong>phagosome</strong></p></li><li><p><strong>Lysosomes </strong>bind to the phagosome to form a <strong>lysophagosome</strong></p></li><li><p>The enzymes in the lysosomes break down the pathogen</p></li><li><p>The products of this bind to the antigens from the macrophage, to form a <strong>major histocompatibility complex (MHC) </strong>in the cytoplasm</p></li><li><p>The macrophage then displays these antigens on the cell membrane to become an <strong>antigen-presenting cell</strong>, which will stimulate lymphocytes in the specific immune response</p></li></ol>
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Where do T and B lymphocytes get produced and mature?

  • Both are produced in the bone marrow

  • B lymphocytes also mature in the bone marrow

  • T lymphocytes mature in the thymus gland

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What are the four types of T lymphocytes and their roles?

  • T helper cells- release interleukins (a type of cytokine), that act as chemical signalling molecules, triggering clonal expansion of T cells and clonal selection of B cells

  • T killer/cytotoxic cells- kill infected body cells by producing perforin (makes holes in the cell membrane of infected cells)

  • T regulator/suppressor cells- suppress (down-regulate) the immune system after the pathogens have been destroyed to prevent an autoimmune response

  • T memory cells- remain in the blood, meaning that if the same pathogen returns the process of clonal selection will occur more quickly

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What are the three types of B lymphocytes and their roles?

  • Plasma cells- produce specific antibodies

  • B effector cells- divide after activation in the humoral immune response to produce plasma cell clones

  • B memory cells- remain in the blood, meaning that if the same pathogen returns the process of clonal selection will occur more quickly

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What is the process of the cell-mediated specific immune response?

  1. Phagocytosis by macrophages produces an antigen-presenting cell

  2. A T helper cell with a specific complementary receptor to the antigen binds during clonal selection

  3. The activated T helper cell produces interleukins (a type of cytokine) which stimulate clonal expansion, where more T cell clones are produced by mitosis

  4. The cloned T cells can develop into any T helper, memory or killer cells

<ol><li><p><strong>Phagocytosis</strong> by macrophages produces an <strong>antigen-presenting cell</strong></p></li><li><p>A <strong>T helper cell </strong>with a specific complementary receptor to the antigen binds during <strong>clonal selection</strong></p></li><li><p>The activated T helper cell produces <strong>interleukins</strong> (a type of cytokine) which stimulate <strong>clonal expansion</strong>, where more T cell clones are produced by mitosis</p></li><li><p>The cloned T cells can develop into any <strong>T helper, memory or killer cells</strong></p></li></ol>
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What is the process of the humoral specific immune response?

  1. A specific B effector cell engulfs an antigen and becomes an antigen-presenting cell (APC)

  2. T helper cells that have been activated during the cell-mediated response bind to the B cell APC, which is clonal selection

  3. The interleukins (a type of cytokine) trigger the B cell to divide by mitosis, in clonal expansion, to become plasma cells and some B memory cells

  4. These plasma cells produce specific antibodies that act against the pathogen

<ol><li><p>A specific <strong>B effector cell</strong> engulfs an antigen and becomes an<strong> antigen-presenting cell </strong>(APC)</p></li><li><p><strong>T helper cells </strong>that have been activated during the cell-mediated response bind to the B cell APC, which is <strong>clonal selection</strong></p></li><li><p>The <strong>interleukins</strong> (a type of cytokine) trigger the B cell to divide by mitosis, in <strong>clonal expansion</strong>, to become plasma cells and some B memory cells</p></li><li><p>These <strong>plasma cells produce specific antibodies</strong> that act against the pathogen</p></li></ol>
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What are the primary and secondary immune responses?

  • The primary response is to a newly encountered antigen

  • The secondary response is to a previously encountered antigen

The primary response produces T and B memory cells, which remain in the blood for a long time

  • This means the process of clonal selection in the secondary response is much faster

  • B memory cells will divide and differentiate into plasma cells to produce antibodies (faster and in greater volumes than the primary response)

  • T memory cells will divide and differentiate into T killer and helper cells

<ul><li><p>The <strong>primary </strong>response is to a <strong>newly </strong>encountered antigen</p></li><li><p>The <strong>secondary </strong>response is to a <strong>previously </strong>encountered antigen</p></li></ul><p>The primary response produces T and B <strong>memory </strong>cells, which remain in the blood for a long time</p><ul><li><p>This means the process of <strong>clonal selection </strong>in the secondary response is much faster </p></li><li><p>B memory cells will divide and differentiate into plasma cells to produce antibodies (faster and in greater volumes than the primary response)</p></li><li><p>T memory cells will divide and differentiate into T killer and helper cells</p></li></ul><p></p>
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What are antibodies and what are their roles?

Antibodies are globular glycoproteins called immunoglobulins, which bind specifically to antigens, and can act as:

  • Opsonins

  • Agglutinins

  • Antitoxins

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What is the structure of antibodies?

  • Y-shaped molecule made up of 4 polypeptide chains- two ‘heavy’ and two ‘light’- joined by strong disulfide bridges

  • Consists of a constant region, which is the same in all antibodies, and a variable region, where the amino acid sequences vary between antibodies to let them bind to specific antigens (at the antigen-binding sites)

  • The hinge region (in the corner between the two heavy chains) gives the structure flexibility so that the Y shape can be at different angles to bind easier

<ul><li><p>Y-shaped molecule made up of <strong>4 polypeptide chains</strong>- two ‘<strong>heavy</strong>’ and two ‘<strong>light</strong>’- joined by strong <strong>disulfide bridges</strong></p></li><li><p>Consists of a<strong> constant region</strong>, which is the same in all antibodies, and a<strong> variable region</strong>, where the amino acid sequences vary between antibodies to let them bind to <strong>specific </strong>antigens (at the <strong>antigen-binding sites)</strong></p></li><li><p>The <strong>hinge region </strong><em>(in the corner between the two heavy chains) </em>gives the structure <strong>flexibility </strong>so that the Y shape can be at different angles to bind easier</p></li></ul>
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How can antibodies act as opsonins?

They can attach to pathogens and tag them so that they are more easily recognisable to phagocytes

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How can antibodies act as agglutins?

They can bind to and clump pathogens together (agglutination), so they are more easily engulfed by phagocytes

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How can antibodies act as antitoxins?

They can bind to the toxins produced by pathogens, neutralising them so that they are harmless

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What is natural active immunity?

When a pathogen enters the body (natural) and triggers an immune response (active)

  • The memory lymphocytes produced cause immunity as the secondary response is much faster

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What is artificial active immunity?

When an antigen enters the body by a vaccination (artificial) and triggers an immune response (active)

  • The memory lymphocytes produced cause immunity as the secondary response is much faster

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What is natural passive immunity?

When a baby receives antibodies (passive) from the mother (natural)

  • This can be received across the placenta, for a foetus, or through colostrum in early breast milk, for newborn babies

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What is artificial passive immunity?

When a person is given antibodies through an injection (artificial) and does not have an immune response (passive)

  • This is sometimes used for people infected with tetanus or rabies

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How do vaccines work?

  • A safe form of antigen, from a pathogen that has been killed, inactivated or attenuated (weakened), is injected into a healthy person

  • This triggers an immune response resulting in the production of memory lymphocytes

  • These remain in the blood and respond quickly to a second exposure

They can provide lifelong or short term protection, in which case routine booster injections may be needed

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How are vaccinations used to prevent epidemics?

Why do some have to be regularly changed?

Why doesn’t everyone in a population need to be vaccinated?

  • At the beginning of an epidemic, mass vaccination can prevent the pathogen from spreading further by making more people immune

  • Pathogens regularly mutate and change their antigens, making vaccines for previous strains useless, so new ones have to be developed regularly (eg. the flu)

  • When the majority of a population has been vaccinated, the chances of a non-vaccinated person encountering the pathogen are so low that they are not at risk- this is herd immunity, which is beneficial for people who cannot be vaccinated (eg. children and immunocompromised people)

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What is an autoimmune disease? What are two examples?

An autoimmune disease occurs when the body attacks itself, because the antibodies or lymphocytes trigger an immune response against a self-antigen

  • Eg. Lupus- the connective tissue of the body is attacked, damaging several organs

  • Eg. Rheumatoid arthritis- the joints are attacked, causing joint pain and muscle spasms

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What causes autoimmune diseases?

The cause is not known but we know:

  • Susceptibility to autoimmune diseases can be inherited and passed down through specific genes

  • It can also be triggered by the environment

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Why is maintaining biodiversity important?

  • Many of our medicines are obtained from plants, bacteria and fungi

  • These plants are mainly tropical, which means deforestation and destruction of rainforest habitats pose a risk to us, as it could kill off a potential source of medicine

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How could genetics affect clinical care?

  • We can look at the genomes of patients and pathogens, to tailor the drug used to the situation

  • People could undergo genetic screening to test whether they have a higher chance of developing specific diseases, so preventative measures could be taken

This is called pharmacogenomics/pharmacogenetics

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What is synthetic biology?

We can genetically modify other organisms, like bacteria, to produce drugs for us

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Why is antibiotic resistance developing?

  • Overuse of antibiotics

  • Use of antibiotics unnecessarily (eg. for viruses)

  • Use of antibiotics on livestock in farming

  • Patients not completing the full prescribed course

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How can biodiversity be considered at different levels?

  • Habitat diversity- the number and range of habitats

  • Species biodiversity- the species richness and evenness within a habitat

  • Genetic biodiversity- the genetic variation within a species

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What are species richness and species evenness?

  • Species richness is the number of different species within an ecosystem (Area 1 and 2 have the same species richness)

  • Species evenness is the distribution of individuals across the different species in an ecosystem (Area 1 has a higher species evenness)

Ecosystems with high species richness and evenness are usually more stable, eg. an ecosystem dominated by only a few species (like Area 2) is at high risk of collapsing if one species is wiped out by a pathogen

<ul><li><p>Species <strong>richness </strong>is the <strong>number </strong>of different species within an ecosystem (Area 1 and 2 have the same species richness)</p></li><li><p>Species <strong>evenness </strong>is the <strong>distribution </strong>of individuals across the different species in an ecosystem (Area 1 has a higher species evenness)</p></li></ul><p>Ecosystems with high species richness and evenness are usually more <strong>stable</strong>, eg. an ecosystem dominated by only a few species (like Area 2) is at high risk of collapsing if one species is wiped out by a pathogen</p>
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What sampling techniques can be used for organisms that can’t be sampled using quadrats?

  • Sweeping nets: used to catch flying insects by sweeping the net through long grass

  • Pitfall traps: jars are buried in the ground and catch insects and other invertebrates as they fall into the trap (canopies stop the trap from filling with rainwater)

  • Pooters: containers with two tubes sticking out- one is placed over the insect and the second tube is sucked to pull the insect into the container

  • Tullgren funnel: soil is placed into a funnel with a lightbulb above- insects will move down away from the light and drop into a container below

  • Kick-sampling: a riverbed is disturbed by kicking, and organisms in the sediment are carried by the water into the net

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How can we assess levels of genetic diversity in isolated populations?

By calculating the proportion of genes in a genome that have multiple alleles (polymorphic loci)

P = the number of polymorphic gene loci ÷ total number of loci sampled

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What are isolated populations?

Populations that have little to no genetic mixing with other organisms of the same species

This can be due to:

  • Captive breeding in zoos, where only a few captive individuals are available

  • Rare breeds and pedigree animals, where organisms are selectively bred together to favour desirable traits

  • Physical isolation, where populations have been geographically separated and can’t interact with each other

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What factors affect biodiversity?

Human population growth has led to an increase in:

  • Agriculture often leads to deforestation, removal of hedgerows, monoculture, herbicides and pesticides, and eutrophication

  • Pollution

  • Climate change results in melting ice caps, rising sea levels, changes in weather conditions (including extreme weather like flooding and droughts), changes to bird migration and insect life cycles, and ocean acidification due to increased CO2 uptake

  • Fish farming

  • Hunting

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What are the economic reasons for maintaining biodiversity?

  • Deforestation leads to soil erosion and desertification, which damages soils so they can’t be used to grow crops

  • Many medicines come from rainforest species, which could go extinct before we find them

  • Lack of diversity in croplands can lead to whole yields being destroyed by one disease or pest

  • Soil depletion due to monoculture strips soil of its nutrients so crops become less successful and healthy

  • Highly biodiverse areas promote tourism

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What are the aesthetic reasons for maintaining biodiversity?

  • Biodiverse areas are popular for recreation, eg. walking, birdwatching, cycling

  • The natural world provides inspiration for creatives such as musicians and poets

  • Patients recover faster from surgery and injury in green areas

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What are the ecological reasons for maintaining biodiversity?

  • A more genetically diverse ecosystem is better able to survive and adapt to environmental changes or threats

  • Organisms are very interdependent, so if one is killed off, it can affect many other organisms

  • This is particularly for keystone species, which play a major role in their ecosystems

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What are the two methods of conservation?

In situ- within the natural habitat

Ex situ- outside of the natural habitat

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What are the methods of in situ conservation?

Wildlife reserves- land is actively managed, including restricting human access, reintroducing species, prohibiting poaching, restricting industrial development, and removing invasive species

Marine conservation zones- areas of water are protected against overfishing and pollution (particularly coral reefs)

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What are the methods of ex situ conservation?

Seed banks- seeds from many different species of plants are dried and frozen to maintain their ability to germinate, so they can be stored for long periods and can be used later on

Botanic gardens- plants are grown in ‘captivity’, under their ideal conditions, to keep populations alive, so they can be researched or reintroduction

Captive breeding programmes- zoos and aquariums maintain stable populations of endangered animal species so they can later be released into the wild (sometimes not possible due to domestication)- genetic diversity is maintained by breeding species from across a network of zoos

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What conservation agreements have been made?

The Rio Convention on Biological Diversity (CBD) was signed by many countries in 1992 to implement strategies to maintain diversity with sustainable development and conservation

The Convention on International Trade in Endangered Species (CITES) is a global agreement that regulates and restricts the trade of at-risk species and their products eg. ivory

The Countryside Stewardship Scheme (CSS) is an initiative local to England, providing funding to farmers and landowners to incentivise conservation in their land management (this has been replaced by the similar Environmental Stewardship Scheme)

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What is the order of taxonomical classification? What is a mnemonic to remember it?

Dear- domain

Kevin- kingdom

Please- phylum

Come- class

Over- order

For- family

Great- genus

Scones- species

<p>Dear- <strong>domain</strong></p><p>Kevin- <strong>kingdom</strong></p><p>Please- <strong>phylum</strong></p><p>Come- <strong>class</strong></p><p>Over- <strong>order</strong></p><p>For- <strong>family</strong></p><p>Great- <strong>genus</strong></p><p>Scones- <strong>species</strong></p>
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What is binomial classification?

  • Each organism is named using two Latin words eg. Canis lupus

  • The first word (capitalised) is the genus

  • The second word is the species

  • The name should be italicised or underlined (if handwritten)

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What is a species?

A group of organisms that are able to reproduce to produce fertile offspring

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Why is the binomial classification system useful?

  • They allow for species to be universally identified

  • The binomial for a species is the same across the globe

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What led to the introduction of the three domain system?

  • Advances in molecular biology, biochemistry and cell structure showed that the prokaryotes are not one singular group

  • Molecular analysis of ribosomal RNA, protein synthesis, responses to antibiotics, and the structure of cell membranes and flagella led to the division of prokaryotes into bacteria and archaea

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What are the three domains? What kingdoms make up each domain?

  • Bacteria- includes kingdom bacteria

  • Archaea- includes kingdom archaea

  • Eukarya- includes kingdoms protoctista, plantae, fungi and animalia

<ul><li><p><strong>Bacteria</strong>- includes kingdom bacteria</p></li><li><p><strong>Archaea</strong>- includes kingdom archaea</p></li><li><p><strong>Eukarya</strong>- includes kingdoms protoctista, plantae, fungi and animalia </p></li></ul>
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Describe the archaea domain

  • Prokaryotic (have no nucleus or membrane bound organelles )

  • Circular DNA

  • 70S ribosomes

  • No cytoskeleton

  • Unique membrane lipids

  • No peptidoglycan in their cell walls

  • RNA polymerase made up by 8-10 proteins

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Describe the bacteria domain

  • Prokaryotic (have no nucleus or membrane bound organelles )

  • Circular DNA

  • 70S ribosomes

  • No cytoskeleton

  • Have peptidoglycan in their cell walls

  • RNA polymerase made up by 5 proteins

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Describe the eukarya domain

  • Eukaryotic (have a membrane-bound nucleus and organelles)

  • Linear DNA

  • 80S ribosomes

  • Have cytoskeleton

  • No peptidoglycan in their cell walls

  • RNA polymerase made up by 12 proteins

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Describe the animalia kingdom

Part of the eukarya domain

  • Eukaryotic

  • No cell wall

  • Multicellular

  • Heterotrophic feeders

  • Store glucose as glycogen

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Describe the plantae kingdom

Part of the eukarya domain

  • Eukaryotic

  • Multicellular

  • Cellulose cell wall

  • Autotrophic feeders (via photosynthesis)

  • Store glucose as starch

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Describe the fungi kingdom

Part of the eukarya domain

  • Eukaryotic

  • Chitin cell wall

  • Can be multi or unicellular

  • Saprophytic, heterotrophic feeders

  • Store glucose as glycogen

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Describe the protoctista kingdom

Part of the eukarya domain

  • Eukaryotic

  • Unicellular (can be in colonies)

  • Autotrophic or heterotrophic feeders

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Describe the old prokaryotae kingdom

  • Prokaryotic

  • Unicellular

  • Circular DNA

  • Heterotrophic or autotrophic feeders

  • Peptidoglycan cell wall

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What are heterotrophs?

  • Organisms that can’t produce their own food

  • They use compounds made by other organisms as their source of energy

  • Heterotrophs include saprophytes (eg. fungi), which rely on dead/decaying matter for food, and parasites

Eg. fungi (saprophytic), animals, some protoctists

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What are autotrophs?

  • Organisms that can produce their own food

  • Most do so via photosynthesis

Eg. plants, some bacteria and protoctists

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What is phylogeny?

The study of the evolutionary history and relationships of organisms

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Why is it good to use phylogenetic classification over Linnaean classification?

  • Phylogenetic trees are continuous, rather than in discrete taxonomical groups- meaning we aren’t forced to put organisms in groups they don’t quite fit

  • The hierarchy of Linnaean classification can be misleading eg. implies two groups in the same rank have the same age, biodiversity and number of species

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Phylogenetic tree

knowt flashcard image
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How was the theory of evolution by natural selection developed?

Charles Darwin and Alfred Wallace conducted independent studies across the world into the variation between species before publishing a paper together proposing the theory of natural selection

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What evidence is there for evolution by natural selection?

The fossil record

Comparative anatomy

Comparative biochemistry

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How can the fossil record be used as evidence for evolution by natural selection?

  • Fossils, and the rocks they are found in, can be dated (less recent layers are deeper in the ground)

  • This lets us accurately order extinct species into a sequence from oldest to youngest, to see how they changed through time

  • This also shows similarities between extinct and living species to see how they have evolved to be better suited for survival

  • However, the fossil record is incomplete as they are unlikely to form and have not all been found

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How can comparative anatomy be used as evidence for evolution by natural selection?

  • Related species share homologous structures, eg. the pentadactyl limb

  • Homologous structures appear different, and may have different purposes, but have the same underlying structure

  • This suggests that the species evolved from a common ancestor that also had that homologous structure

<ul><li><p>Related species share <strong>homologous structures</strong>, eg. the <strong>pentadactyl</strong> limb</p></li><li><p>Homologous structures appear different, and may have different purposes, but have the same <strong>underlying structure</strong></p></li><li><p>This suggests that the species evolved from a <strong>common ancestor </strong>that also had that homologous structure</p></li></ul>
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How can comparative biochemistry be used as evidence for evolution by natural selection?

  • The bases in DNA strands and the amino acids in proteins can be sequenced

  • The differences between these sequences in the equivalent genes of different species can show how closely related they are:

    • The more similar the sequence the more closely related the species are

  • Ribosomal RNA and cytochrome c, a protein involved in respiration, are the most commonly compared, as they are almost universal

<ul><li><p>The <strong>bases in DNA strands </strong>and the <strong>amino acids</strong> in proteins can be sequenced</p></li><li><p>The <strong>differences</strong> between these <strong>sequences</strong> in the equivalent genes of different <strong>species</strong> can show how closely related they are:</p><ul><li><p><strong>The more similar the sequence the more closely related the species are</strong></p></li></ul></li><li><p><strong>Ribosomal RNA and cytochrome c</strong>, a protein involved in respiration, are the most commonly compared, as they are almost universal</p></li></ul>
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What are the two types of species variation?

Interspecific- variation between different species

Intraspecific- variation between individuals in the same species

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What are continuous and discontinuous variation? What causes them?

Continuous- can be any value across a range eg. between 1 and 10

  • Caused by more than two genes (polygenic) and often by environmental factors

Discontinuous- falls into discrete groups eg. red or green

  • Caused only by one gene

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What are the different types of adaptations?

Anatomical

  • Structural or physical features

  • Eg. Having spines, camouflage, thick fur

Physiological

  • Biological processes

  • Eg. Producing poison or antibiotics, holding water

Behavioural

  • How an organism acts

  • Eg. Being nocturnal, migration, courtship rituals

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What is convergent and divergent evolution? Give an example of each

Divergent evolution- when species appear similar because they inherited traits from a recent common ancestor

  • Eg. the pentadactyl limb

Convergent evolution- when species appear similar due to having adapted certain traits for their habitat, even though they don’t share a recent common ancestor

  • Eg. the marsupial vs placental mole

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What is the process of evolution by natural selection?

  • There’s variation in the population due to mutations introducing new alleles

  • A selection pressure (change in environment eg. climate, disease, food availability) kills off most of the population

  • Certain individuals have alleles that are advantageous and they survive

  • These individuals breed and their offspring inherit the beneficial alleles

  • Over many generations this repeats and the frequency of the trait in the population increases

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How can a population evolve antibiotic or pesticide resistance?

  • There’s variation in the population due to mutations introducing new alleles

  • The antibiotic or pesticide acts as a selection pressure and kills off most of the population

  • Certain individuals have resistant alleles that are advantageous and they survive

  • These individuals breed and their offspring inherit the resistant alleles

  • Over many generations this repeats and the frequency of resistance in the population increases