IQ: What is the evidence that supports the Theory of Evolution by Natural Selection?
4.1 investigate, using secondary sources, evidence in support of Darwin and Wallace’s Theory of Evolution by Natural Selection, including but not limited to:
a) biochemical evidence, comparative anatomy, comparative embryology and biogeography (ACSBL089)
b) techniques used to date fossils and the evidence produced
4.2 explain modern-day examples that demonstrate evolutionary change, for example:
a) the cane toad
b) antibiotic-resistant strains of bacteria
4.1 investigate, using secondary sources, evidence in support of Darwin and Wallace’s Theory of Evolution by Natural Selection, including but not limited to:
a) biochemical evidence, comparative anatomy, comparative embryology and bio-geography
Modern evolutionary theory states that all living organisms share a common origin that dates back to around 3800 million years ago. These earliest organisms were bacteria, but over millions of years they diverged. Some became extinct, others continued to diverge in ever-branching lines of descent to those we have today.
Many different forms of evidence have come together to provide the modern theory of evolution. These include
a) biochemical evidence, comparative anatomy, comparative embryology and bio-geography
b) techniques used to date fossils and the evidence produced
Summary:
Certain parts of our DNA sequence called genes each code for a unique sequence of amino acids called a polypeptide chain. These polypeptides fold into proteins that ultimately regulate our cellular functions thereby determining our characteristics.
Evolution relies on mutations that alter the DNA sequence producing a new protein with an altered function. If the new function coveys some adaptive advantage it will be selected for (see natural selection)
However, not all mutations actually alter the amino acid sequence or structure of a protein. Therefore not every difference in the DNA sequence of two species represents an evolutionary change. Comparing the amino acid sequence or protein structures of two organisms gives a more accurate idea of their evolutionary relatedness.
Detail:
Biologists use the DNA sequences of modern organisms to reconstruct the tree of life and to figure out the likely characteristics of the most recent common ancestor of all living things — the "trunk" of the tree of life. In fact, according to some hypotheses, this "most recent common ancestor" may actually be a set of organisms that lived at the same time and were able to swap genes easily. In either case, reconstructing the early branches on the tree of life tells us that this ancestor (or set of ancestors) probably used DNA as its genetic material and performed complex chemical reactions. But what came before it? We know that this last common ancestor must have had ancestors of its own - a long line of forebears forming the root of the tree of life - but to learn about them, we must turn to other lines of evidence.
Evolutionary Lines of Descent
There are certain key molecules and biochemical mechanisms shared by incredibly different organisms. Many of the chemical reactions occurring in human cells, in the cells of a fungus, and in a bacterial cell are quite different from one another; however, many of them are exactly the same and rely on the exact same molecules - photosynthesis and cellular respiration are identical or very similar in quite different types of organisms, all organisms use DNA and/or RNA for their genetic code; ATP, essential for powering cellular processes, is used by all modern life.
Because these molecules are widespread and are critically important to all life, they are thought to have arisen very early in the history of life.
Read https://evolution.berkeley.edu/evolibrary/article/0_0_0/origsoflife_06
View video:
What is the RNA world hypothesis? https://www.youtube.com/watch?v=K1xnYFCZ9Yg [7.08 mins]
The current view is that an RNA world existed on Earth before modern cells arose. According to this hypothesis, RNA stored both genetic information and catalysed the chemical reactions in primitive cells. Only later in evolutionary time did DNA take over as the genetic material and proteins become the major catalyst and structural component of cells. If this idea is correct, then the transition out of the RNA world was never complete; RNA still catalyzes several fundamental reactions in modern-day cells, which can be viewed as 'molecular fossils; of an earlier world.
From https://www.ncbi.nlm.nih.gov/books/NBK26876/"Experiments can help scientists figure out how the molecules involved in the RNA world arose. These experiments serve as "proofs of concept" for hypotheses about steps in the origin of life — in other words, if a particular chemical reaction happens in a modern lab under conditions similar to those on early Earth, the same reaction could have happened on early Earth, and could have played a role in the origin of life."
From https://evolution.berkeley.edu/evolibrary/article/0_0_0/origsoflife_07In the 1950's, biochemists Stanley Miller and Harold Urey, conducted an experiment which demonstrated that several organic compounds could be formed spontaneously by simulating the conditions of Earth's early atmosphere.
They designed an apparatus which held a mix of gases similar to those found in Earth's early atmosphere over a pool of water, representing Earth's early ocean. Electrodes delivered an electric current, simulating lightning, into the gas-filled chamber. After allowing the experiment to run for one week, they analyzed the contents of the liquid pool. They found that several organic amino acids had formed spontaneously from inorganic raw materials. These molecules collected together in the pool of water, suggesting complex molecules could have formed in early Earth.
From https://www.windows2universe.org/earth/Life/miller_urey.html Images below are diagrams of the experiments.View video:
Molecular evidence https://www.youtube.com/watch?v=zhAx8Toxcho [2.58]
Work through the examples from Khan Academy
Comparing the body structures (anatomy) of different species also supports the notion (idea) of a common ancestor. Closely related species have more anatomical (structural) similarities. Even less closely related species show evidence of underlying anatomical similarities, with common structural features that have been modified for a different function / purpose.
Anatomical features that are derived from a common ancestor but have been adapted to a different purpose are called homologous structures.
The pentadactyl (5-digit) limb found in most vertebrates (animals with a backbone) has the same general bone structure / pattern. However, the size and shape of each bone has modified to serve a slightly different function.
These "homologues" indicate that all of these species diverged from a common ancestor (adaptive radiation) and that the basic limb plan has adapted to meet the needs of different niches.
Some animals possess inherited features that they no longer need.
Whales still have the remains of a hip bone. It is significantly reduced (smaller), but serves no known function. This is evidence that whales have evolved from a once four-legged ancestor. The hind legs and hips have steadily become smaller and may one day be eliminated entirely. For now, whales are stuck with this "evolutionary baggage".
A major problem in determining evolutionary relationships based on comparative anatomy can be seen when we look at a common structure: the wing. Wings are present in a number of very different groups of organisms. Birds, bats and insects all have wings, but what does this say about how closely related the three groups are? It is tempting to say that the three groups must have had a common winged ancestor. However, the wings of bats and birds are both derived from the forelimb of a common, probably wingless, ancestor. Both have wings with bone structures similar to the forelimbs of ancestral and current tetrapod, or four-legged, animals. These are homologous traits.
Structurally speaking, though, the wings of bats and birds have little in common with those of insects. Bird wings and insect wings are an analogous trait, or a trait that has developed independently in two groups of organisms from unrelated ancestral traits. (Analogous Structures are features that have a very similar function but completely different anatomy. They normally occur when distantly related species occupy a similar environment.)
From https://www.pathwayz.org/Tree/Plain/EVIDENCE+FOR+EVOLUTIONView video:
Comparative anatomy https://www.youtube.com/watch?v=z_gHu7MSkWg [2.33]
Complete worksheet at right.
Option: Comparing vertebrate hearts activity WS https://www.teacherspayteachers.com/Product/Comparing-Vertebrate-Hearts-3163327 $1.50
Complete Quiz:
Homologous and Analogous Structures
All species start out as single celled organisms, zygotes. Many species develop into much larger, more complex organisms after conception. If we compare the embryos of animals as they develop, we often find they are much more similar than their fully developed counterparts. Many of the anatomical differences between species only arise during our embryonic development. Different species often start with the same basic tissues or structures but they develop differently and are re-purposed into different structures as the organism develops. The more closely two species are related the later in development these differences usually emerge. This too supports the idea that we are descendants with modified structures that were inherited form a common ancestor.
Another difficulty in comparing traits between species rests on the fact that homologous structures not present in the adult organism often do appear in some stage of embryonic development. In this way, the embryo serves as a microcosm for evolution, passing through many of the stages of evolution to produce the current state of the organism. Species that bear little resemblance in their adult form may have strikingly similar embryonic stages. For example, in humans, the embryo passes through a stage in which it has gill structures like those of the fish from which all terrestrial animals evolved. For a large portion of its development the human embryo also possesses a tail, much like those of our close primate relatives. This tail is usually reabsorbed before birth, but occasionally children are born with the ancestral structure intact. Tails and even gills could be considered homologous traits between humans and primates or humans and fish, even though they are not present in the adult organism.
If you were to compare the embryos of these animals at what point do you think you could pick which one is human?
View videos:
What is comparative embryology https://www.youtube.com/watch?v=x-7qTuy0ps0 [2.32]
What can embryos tell us https://www.youtube.com/watch?v=uAZmLYWEPGk [3.43]
Evolution: genetics, embryos... https://www.youtube.com/watch?v=xrEp_yMtbts [4.42]
The field of biogeography is concerned with the distribution of species in relation both to geography and to other species - historical biogeography is concerned with the origins and evolutionary histories of species on a long time scale.
Historical biogeographers depend heavily on evidence from other disciplines. Fossil records provide a large part of the information needed to determine distributions and past interactions. Molecular Biology furnished historical biogeographers with molecular clocks, metabolic molecules whose change over time help track the relatedness of species.
Adapted from https://www.sparknotes.com/biology/evolution/evidence/section2/The geographic distribution of organisms on Earth follows patterns that are best explained by evolution, in combination with the movement of tectonic plates over geological time. For example, broad groupings of organisms that had already evolved before the breaking apart of the supercontinent Pangaea (about 200 million years ago) tend to be distributed worldwide. In contrast, broad groupings that evolved after the break tend to appear uniquely in smaller regions of Earth: there are unique groups of plants and animals on northern and southern continents that can be traced to the split of Pangaea into two supercontinents (Laurasia in the north, Gondwana in the south).
The evolution of unique species on islands is another example of how evolution and geography intersect. Most of the mammal species in Australia are marsupials (carry young in a pouch), while most mammal species elsewhere in the world are placental (nourish young through a placenta). Australia’s marsupial species are very diverse and fill a wide range of ecological roles. Because Australia was isolated by water for millions of years, these species were able to evolve without competition from (or exchange with) mammal species elsewhere in the world.
The marsupials of Australia, Darwin's finches in the Galápagos, and many species on the Hawaiian Islands are unique to their island settings, but have distant relationships to ancestral species on mainlands. This combination of features reflects the processes by which island species evolve. They often arise from mainland ancestors – for example, when a landmass breaks off or a few individuals are blown off course during a storm – and diverge (become increasingly different) as they adapt in isolation to the island environment.
Adapted from https://www.khanacademy.org/science/biology/her/evolution-and-natural-selection/a/lines-of-evidence-for-evolutionView Slideshare:
Evidence of Evolution: Biogeography https://www.slideshare.net/mrtangextrahelp/02-evidence-of-evolution-biogeography?qid=c145f392-6ba3-403d-a30e-09a6176db6bf&v=&b=&from_search=3
View videos:
Biogeography: Where life lives https://www.khanacademy.org/science/high-school-biology/hs-evolution/hs-evidence-of-evolution/v/biogeography-where-life-lives [1.49mins]
The invisible line https://www.youtube.com/watch?v=6vcMQboy2Jg [4.52]
Visit:
Evidence for Evolution: (not 0-2.36 fossils) https://www.youtube.com/watch?v=O21VOcLIb3M [2.36 to 5.25 of 5.25mins]
View video:
Cash course: Evolution - it's a thing https://www.youtube.com/watch?v=P3GagfbA2vo [11.53 mins]
1. Compile a table with title 'Evidences for Evolution', and headings:
Type (include fossil evidence, which will be considered in 4.1b)
Description
Support for evolution
2. Explain why monotremes are unique to the Australian biogeographical reagion.
4.1 investigate, using secondary sources, evidence in support of Darwin and Wallace’s Theory of Evolution by Natural Selection, including but not limited to:
b) techniques used to date fossils and the evidence produced
Generally, we think of bones, shells, or teeth that are buried in rock, but fossils can also be outlines of leaves or footprints or trails. This second set of fossils, which are the outlines of items from the past rather than the items themselves, are called trace fossils. Fossils are formed when sediment covers some material, such as a piece of bone. Very gradually, the bone becomes impregnated with chemicals from the surrounding rock. Eventually all that remains is essentially a piece of rock in the shape of the original bone, or material.
The fossil record provides snapshots of the past that, when assembled, illustrate a panorama of evolutionary change over the past four billion years. The picture may be smudged in places and may have bits missing, but fossil evidence clearly shows that life is old and has changed over time. Whereas molecular biology might be used to study microevolution, or the development of individual species, paleontology is used to study macroevolution, or large evolutionary trends.
Taken together, fossils can be used to construct a fossil record, which is a timeline of fossils reaching back through history. Several factors must be taken into account when constructing such a record. The strata of rock in which fossils are found give us clues about their relative ages. Similarly, technological techniques such as radioactive carbon dating help determine the absolute ages of fossils. In addition to supplying a fossil's relative age, rock strata can also give clues about the environments in which an animal or plant lived. The chemical make-up of these strata can tell us the balance of gases in ancient atmospheres. Major cataclysmic events such as eruptions and meteor strikes also leave their mark on the fossil record.
There are, however, limitations on the information fossils can supply. Fossilisation is an improbable event. Most often, bones and other materials are crushed or consumed before they can be fossilised. In addition, fossils can only form in areas where sedimentary rock is formed, such as ocean floors. Organisms that live in these environments are therefore more likely to be fossilised. Erosion of exposed rock faces or through the crushing action of geological movements can destroy fossils even after they are formed. All of these conditions lead to large and numerous gaps in the fossil record.
In the 1600s, Nicholas Steno shook the world of science, noting the similarity between shark teeth and the rocks commonly known as "tongue stones."
This was our first understanding that fossils were a record of past life.
Two centuries later, Mary Ann Mantell picked up a tooth, which her husband Gideon thought to be of a large iguana, but it turned out to be the tooth of a dinosaur, Iguanodon. This discovery sent the powerful message that many fossils represented forms of life that are no longer with us today.
View video:
Knowing when a dinosaur or other animal lived is important because it helps place them on the evolutionary family tree. Accurate dates also enable sequences of evolutionary change to be created and when species appeared or became extinct to be determined.
There are two main methods to date a fossil. These are:
Relative dating methods: used to determine a fossil's approximate age by comparing it to similar rocks and fossils of known ages. These can only tell whether one object is older or younger than another – they cannot pinpoint an actual age in years. Relative dating methods are used to work out the chronological sequence of fossils. They can be applied to fossils found at a particular site and can also be used to make comparisons between sites.
Absolute dating methods: used to determine a precise age of a fossil by using radiometric dating to measure the decay of isotopes, either within the fossil or more often the rocks associated with it. These tell us the actual age (in years) of an object. There are many absolute dating methods, nearly all make use of radioactive elements that occur naturally in various types of minerals and organic matter.
Where possible, several different methods are used and each method is repeated to confirm the results obtained and improve accuracy. Different methods have their own limitations, especially with regard to the age range they can measure and the substances they can date. A common problem with any dating method is that a sample may be contaminated with older or younger material and give a false age. This problem is now reduced by the careful collection of samples, rigorous crosschecking and the use of newer techniques that can date minute samples.
The majority of the time fossils are dated using relative dating techniques. Using relative dating the fossil is compared to something for which an age is already known.
Chemical analysis: In special cases, bones can be compared by measuring chemicals within them. Buried bones absorb chemicals, such as uranium and fluorine, from the surrounding ground and absorb more of these chemicals the longer they remain buried. The rates of absorption depend on a number of factors which are too variable to provide absolute dates. This technique is, however, useful for providing relative dates for objects found at the same site.
Another useful chemical analysis technique involves calculating the amount of nitrogen within a bone. The level of nitrogen gradually reduces as the bone decays. Absolute dating is not possible with this method because the rate at which the nitrogen content declines depends on the surrounding temperature, moisture, soil chemicals and bacteria. The technique can, however, provide the relative ages of bones from the same site.
Stratigraphy: Most fossils are found in sedimentary rocks deposited in layers. Where the rocks are not strongly folded or tilted it is possible to work out the order in which the layers were formed. The oldest rocks and fossils are at the bottom and the youngest are on top.
Biostratigraphy: Scientists are able to recognise fossils that are characteristic of various rock layers. With this knowledge, they can place the fossils into detailed chronological sequences. These known sequences can be compared with the layers of rock and fossils uncovered at other sites to provide relative dating. Some fossils are particularly useful for these comparisons as they show distinct changes over time.
Scientists can use certain types of fossils referred to as index fossils to assist in relative dating via correlation. Index fossils are fossils that are known to only occur within a very specific age range. Typically commonly occurring fossils that had a widespread geographic distribution, such as brachiopods, trilobites, and ammonites, work best as index fossils. If the fossil you are trying to date occurs alongside one of these index fossils, then the fossil you are dating falls into the age range of the index fossil.
Sometimes multiple index fossils can be used. In a hypothetical example, a rock formation contains fossils of a type of brachiopod known to occur between 410 and 420 million years. The same rock formation also contains a type of trilobite that was known to live 415 to 425 million years ago. Since the rock formation contains both types of fossils the ago of the rock formation must be in the overlapping date range of 415 to 420 million years.
https://australianmuseum.net.au/learn/australia-over-time/fossils/dating-dinosaurs-and-other-fossils/View videos:
Absolute dating is used to determine a precise age of a rock or fossil through radiometric dating methods. This uses radioactive minerals that occur in rocks and fossils almost like a geological clock. It’s often much easier to date volcanic rocks than the fossils themselves or the sedimentary rocks they are found in. So, often layers of volcanic rocks above and below the layers containing fossils can be dated to provide a date range for the fossil containing rocks.
Fission track: Uranium is present in many different rocks and minerals, usually in the form of uranium-238. This form of uranium usually decays into a stable lead isotope but the uranium atoms can also split – a process known as fission. During this process the pieces of the atom move apart at high speed, causing damage to the rock or mineral. This damage is in the form of tiny marks called fission tracks. When volcanic rocks and minerals are formed, they do not contain fission tracks. The number of tracks increases over time at a rate that depends on the uranium content. It is possible to calculate the age of a sample by measuring the uranium content and the density of the fission tracks.
Potassium-argon dating: The age of volcanic rocks and ash can be determined by measuring the proportions of argon (in the form of argon-40) and radioactive potassium within them. Each volcanic eruption produces a new deposit of ash and rock. Fossils and other objects that accumulate between these eruptions lie between two different layers of volcanic ash and rock. An object can be given an approximate date by dating the volcanic layers occurring above and below the object.
Argon is gas that gradually builds up within rocks from the decay of radioactive potassium. It is initially formed in the molten rock that lies beneath the Earth’s crust. The heat from a volcanic eruption releases all the argon from the molten rock and disperses it into the atmosphere. Argon then starts to re-accumulate at a constant rate in the newly formed rock that is created after the eruption.
Argon-argon dating: This relatively new technique was developed in order to achieve more accurate dates than those obtained from the potassium-argon method. The older method required two samples for dating and could produce imprecise dates if the argon was not fully extracted. This newer method converts a stable form of potassium (potassium-39) into argon-39. Measuring the proportions of argon-39 and argon-40 within a sample allows the age of the sample to be determined. Only one sample is required for this method as both the argon-39 and argon-40 can be extracted from the same sample.
https://australianmuseum.net.au/learn/australia-over-time/fossils/dating-dinosaurs-and-other-fossils/View Slidshow:
Radioactive Decay https://slideplayer.com/slide/6843087/
View video:
K-Ar Dating https://www.khanacademy.org/science/biology/history-of-life-on-earth/ [10.34 mins]
View videos:
How do palaentologists date fossils? https://www.youtube.com/watch?v=f0-dFJRGsYk [1.37 mins]
Radiometric dating https://www.youtube.com/watch?v=8QnsA_1pEd8 [6.06mins]
Fossil dating https://www.khanacademy.org/science/in-in-class-10-biology/in-in-heredity-and-evolution/in-in-evolution-classification/v/fossil-dating-heredity-evolution-biology-khan-academy [4.18 to 9.14 of 9.14 mins]
View videos:
Evidence of Evolution https://www.youtube.com/watch?v=cC8k2Sb1oQ8 [9.22 mins]
What is the Evidence for Evolution? https://www.youtube.com/watch?v=lIEoO5KdPvg&t=556s [11.21 mins]
The evolutionry evidences, taken together, allow scientists to build phylogenetic trees. These are hypotheses, not laws or theories.
A phylogenetic tree is a diagram that represents evolutionary relationships among organisms.
The pattern of branching in a phylogenetic tree reflects how species or other groups most probably evolved from a series of common ancestors.
In trees, two species are more related if they have a more recent common ancestor and less related if they have a less recent common ancestor.
In a phylogenetic tree, the species or groups of interest are found at the tips of lines referred to as the tree's branches.
The pattern in which the branches connect represents our understanding of how the species in the tree evolved from a series of common ancestors. Each branch point (also called an internal node) represents a divergence event, or splitting apart of a single group into two descendant groups.
At each branch point lies the most recent common ancestor of all the groups descended from that branch point. For instance, at the branch point giving rise to species A and B, we would find the most recent common ancestor of those two species. At the branch point right above the root of the tree, we would find the most recent common ancestor of all the species in the tree (A, B, C, D). Each horizontal line in our tree represents a series of ancestors, leading up to the species at its end. For instance, the line leading up to species E represents the species' ancestors since it diverged from the other species in the tree. Similarly, the root represents a series of ancestors leading up to the most recent common ancestor of all the species in the tree.
View Slideplayer: https://slideplayer.com/slide/16571528/
4.2 explain modern-day examples that demonstrate evolutionary change, for example:
a) antibiotic-resistant strains of bacteria
Natural selection increases the frequency of characteristics that make individuals better adapted and decreases the frequency of other characteristics, leading to changes within the species
The key components to the process of natural selection are ICE AGE:
Inherited variation exists within the population
Competition results from an overproduction of offspring
Environmental pressures lead to differential reproduction
Adaptations which benefit survival are selected for
Genotype frequency changes across generations
Evolution occurs within the population
The development of bacterial resistance to antibiotics is direct evidence for evolution by the process of natural selection.
Overview:
Antibiotic resistance is one of the biggest threats to global health, food security, and development today.
Antibiotic resistance occurs naturally, but misuse of antibiotics in humans and animals is accelerating the process.
A growing number of infections – such as pneumonia, tuberculosis, gonorrhoea, and salmonellosis – are becoming harder to treat as the antibiotics used to treat them become less effective.
View video:
Watch antibiotic resistance evolve https://www.youtube.com/watch?v=yybsSqcB7mE [2.03 mins]
1. Read the article in the drop down box (click arrow at right) from Science Daily: https://www.sciencedaily.com/terms/antibiotic_resistance.htm
2. Explain why the development of antibiotic resistance is an example of Darwinian evolution.
Antibiotic resistance is the ability of a microorganism to withstand the effects of an antibiotic.
It is a specific type of drug resistance.
Antibiotic resistance evolves naturally via natural selection through random mutation, but it could also be engineered by applying an evolutionary stress on a population.
Once such a gene is generated, bacteria can then transfer the genetic information in a horizontal fashion (between individuals) by plasmid exchange.
If a bacterium carries several resistance genes, it is called multiresistant or, informally, a superbug.
Causes:
Antibiotic resistance can also be introduced artificially into a microorganism through transformation protocols.
This can be a useful way of implanting artificial genes into the microorganism.
Antibiotic resistance is a consequence of evolution via natural selection.
The antibiotic action is an environmental pressure; those bacteria which have a mutation allowing them to survive will live on to reproduce.
They will then pass this trait to their offspring, which will be a fully resistant generation.
Several studies have demonstrated that patterns of antibiotic usage greatly affect the number of resistant organisms which develop.
Overuse of broad-spectrum antibiotics, such as second- and third-generation cephalosporins, greatly hastens the development of methicillin resistance.
Other factors contributing towards resistance include incorrect diagnosis, unnecessary prescriptions, improper use of antibiotics by patients, and the use of antibiotics as livestock food additives for growth promotion.
Researchers have recently demonstrated the bacterial protein LexA may play a key role in the acquisition of bacterial mutations. Resistant pathogens Staphylococcus aureus (colloquially known as "Staph aureus" or a Staph infection) is one of the major resistant pathogens. Found on the mucous membranes and the skin of around a third of the population, it is extremely adaptable to antibiotic pressure. It was the first bacterium in which penicillin resistance was found—in 1947, just four years after the drug started being mass-produced.
Methicillin was then the antibiotic of choice (but has since been replaced by oxacillin due to significant kidney toxicity). MRSA (methicillin-resistant Staphylococcus aureus) was first detected in Britain in 1961 and is now "quite common" in hospitals. MRSA was responsible for 37% of fatal cases of blood poisoning in the UK in 1999, up from 4% in 1991.
Half of all S. aureus infections in the US are resistant to penicillin, methicillin, tetracycline and erythromycin. This left vancomycin as the only effective agent available at the time.
However, strains with intermediate (4-8 ug/ml) levels of resistence, termed GISA (glycopeptide intermediate Staphylococcus aureus) or VISA (vancomycin intermediate Staphylococcus aureus), began appearing the the late 1990s. The first identified case was in Japan in 1996, and strains have since been found in hospitals in England, France and the US. The first documented strain with complete resistance to vancomycin, termed VRSA (Vancomycin-resistant Staphylococcus aureus) appeared in the United States in 2002.
A new class of antibiotics, oxazolidinones, became available in the 1990s, and the first commercially available oxazolidinone, linezolid, is comparable to vancomycin in effectiveness against MRSA. Linezolid-resistance in Staphylococcus aureus was reported in 2003.
CA-MRSA (Community-acquired MRSA) has now emerged as an epidemic that is responsible for rapidly progressive, fatal diseases including necrotising pneumonia, severe sepsis and necrotising fasciitis.
Methicillin-resistant Staphylococcus aureus (MRSA) is the most frequently identified antimicrobial drug-resistant pathogen in US hospitals. In the past 10 years, infections caused by this organism have emerged in the community. Outbreaks of community-associated (CA)-MRSA infections have been reported in correctional facilities, among athletic teams, among military recruits, in newborn nurseries.
CA-MRSA infections now appear to be endemic in many urban regions and cause most CA-S. aureus infections.
4.2 explain modern-day examples that demonstrate evolutionary change, for example:
b) the cane toad
Article 1: https://www.canetoadsinoz.com/cane-toads-caused-evolution.html in drop down box
Not only have cane toads evolved rapidly; also, they have caused rapid evolution in native animals in the course of their Australian invasion.
We know that toads kill lots of native predators that try to eat the toxic invaders, but cannot tolerate the toads’ poisons. Animals that try to eat big toads, like quolls and goannas, are in the biggest trouble (because big toads have a lot more poison than small toads). However, not every predator is equally vulnerable. Some are reluctant to try to eat toads; others are a bit more tolerant than usual of the toads’ poison, and so forth. In evolutionary biology jargon, this means that cane toads in Australia are a “selective pressure”. That is, the arrival of toads removes some genetic traits from the predator population (genes that make predators vulnerable to toads) but other traits (e.g., genes that tell the predator not to eat toads) are not affected. So, the toads cause a change in genetic composition of the predators: the only ones that survive are the ones that are able to live side-by-side with toads.
What kinds of characteristics would help a predator to survive after the cane toads arrive? The obvious characteristics would be genes that help predators ignore toads as food, and that allow predators to survive a dose of toad poison. But probably lots of characteristics might play a role … for example, any gene affecting where and when a predator is active (if it’s best not to overlap too much with toads) might help the predator to survive. Another “toad-smart” characteristic would be any gene that reduced the size of toads that a predator could eat – because smaller toads have much less poison than larger animals.
The best evidence on this evolutionary process comes from Dr Ben Phillips’ studies on red-bellied blacksnakes, a venomous snake species from eastern Australia. Ben looked at animals from Queensland (where the snakes lived in toad-infested areas) and New South Wales (where there are large areas where the snakes occur but toads do not – or at least, not yet). Ben found exactly the kinds of differences between snakes from toad-infested and non-infested areas that we would expect from evolutionary change. First, the snakes that lived with toads wouldn’t eat toads when we offered them to snakes in captivity, whereas when given the chance, about half of the snakes from toad-free areas readily grabbed a toad – and usually died as a result. Second, the toad-exposed snakes were more able to deal with the toads’ poison. Third, the snakes from toad areas had smaller heads compared to their body size – so they were not able to eat really big (and thus, more dangerous) toads.
The ability of native animals to evolve rapidly to deal with toads is a really encouraging result in terms of biodiversity and conservation. Toads haven’t driven any species to extinction – instead, they reduce predator numbers and change their characteristics. After some time (and we really don’t know how long), the predators are able to coexist with toads, and so their numbers begin to recover.
Cane toads in the Northern Territory and Western Australia have evolved "very very rapidly" to hop in a straight line and cover up to six times more ground than distant cousins back in Queensland, scientists say.
Research published in the Proceedings of the Royal Society of London journal shows "a new kind of evolution" and a phenomenon dubbed "spatial sorting", according to the article's co-author and University of Sydney professor Rick Shine.
"The front has accelerated from about 10-15 kilometres per year to about 60 kilometres per year over the time toads have been in Australia," Professor Shine said. "To move at that rate, toads have to behave in very strange ways - ways that no other frog has before. All you get at the front are the offspring of the fastest toads who were themselves the offspring of the fastest toads who themselves were the offspring of the fastest toads. Genes for fast dispersal end up concentrated at the invasion front. This is evolution through space rather than time. It's quite different to the sorts of things (Charles) Darwin talked about. Cane toads are the best example in the world of this new evolutionary process."
Cane toads in Australia have proven to be one of the best biological systems anywhere in the world, for studies on rapid evolutionary change. Australian cane toads are now turning up in lots of textbooks of evolutionary biology.