| TIME | EVENT DESCRIPTION | LOCATION | IMAGES |
UNIVERSE | |||
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1,000,000,000,000 YBN | 1) We are a tiny part of a universe made of an infinite amount of space, matter and time. | ||
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995,000,000,000 YBN | 11) There is no time I can identify as the start of the universe, the universe has no beginning and no end; perhaps the same photons that have always been in the universe continue to move in the space that has always been. | ||
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990,000,000,000 YBN | 2) There is more space than matter. | ||
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980,000,000,000 YBN | 3) All of the matter is made of particles of light humans have named "photons". Photons are the base unit of all matter from the tiniest particles to the largest galaxies.1 FOO TNOTES 1. ^ Ted Huntington. | ||
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960,000,000,001 YBN | 5) Photons generally move 300 million meters every second in a line, but as pieces of matter, can be slightly slowed from the force of gravity, and stop for an instant when they collide.1 FOOTNOTES 1. ^ Ted Huntington | ||
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950,000,000,000 YBN | 6) Matter is attracted to other matter and so photons form structures such as protons, atoms, molecules, molecule groups (like all of life of earth), planets, stars, galaxies, and clusters of galaxies. | ||
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940,000,000,000 YBN | 7) All of the hundreds of billions of galaxies we can see are only a tiny part of the universe. 1 Most of the galaxies in the universe we will never see because they are too far away for even 1 particle of light from them to be going in the exact direction of our tiny location, or are captured by atoms between here and there. 2 FOOTNOTES 1. ^ Carl Sagan, "Cosmos", Carl Sagan Productions, KCET Los Angeles, (1980). (estimate of how many galaxies) 2. ^ Ted Huntington | ||
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935,000,000,000 YBN | 4) The patterns in the universe are clear. Photons form gas clouds of Hydrogen and Helium, these gas clouds, called nebuli condense to form galaxies of stars. The stars emit photons back out into the rest of the universe, where they collect and form clouds again. Around each star are many planets and pieces of matter. On many of those planets intelligent life evolves. This life moves their stars out of spiral galaxies to form globular clusters, and ultimately to transform spiral galaxies into elliptical galaxies that travel the universe looking for more matter to fuel their movement. It may very well be that stars at this scale are photons, spiral galaxies charged particles, globular galaxies neutral particles, and galactic clusters atoms at a much larger scale in an infinite macro and micro scale.1 FOOTNOTES 1. ^ Ted Huntington | ||
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880,000,000,000 YBN | 13) The Milky Way Galaxy forms, perhaps from a gas cloud that formed by capturing matter in the form of light from other stars, from the remains of a previously destroyed galaxy, or some combination of the two. | ||
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5,500,000,000 YBN 1 | 16) The yellow star earth will eventually orbit forms, perhaps in a nebula, when matter in the nebula starts accumulating and rotating as a result of gravity, or from the remains of an exploded star that condensed again under the influence of gravity. FOOTNOTES 1. ^ Ted Huntington | ||
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5,000,000,000 YBN | 22) Heavier atoms in the star system move closer to the center and lighter atoms are sent farther out. | ||
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4,600,000,000 YBN | 17) Planets form around star. Terrestrial planets are red hot, have surface of melted rock, all lighter atoms float to the surface of the molten planets. All the H2O from the first earth oceans and lakes is in the atmosphere in gas form. | ||
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4,600,000,000 YBN | 30) Moon of earth is formed by 1 of 3 ways: 1) spherical planet collides with earth, moon forms from remaining matter in ring around earth. 2) spherical planet is caught in earth orbit 3) moon of earth forms naturally from original matter of star system in orbit around earth. | ||
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4,571,000,000 YBN 3 4 | 31) Oldest meteorite yet found on earth 4,571 million years old.1 2 FOOTNOTES 1. ^ http://www.sciencemag.org/cgi/content/fu ll/288/5472/1819?maxtoshow=&HITS=10&hits =10&RESULTFORMAT=&fulltext=zag+morocco&s earchid=1129920472874_9236&stored_search =&FIRSTINDEX=0#RF2 2. ^ http://news.bbc.co.uk/1/hi/sci/tech/7830 48.stm 3. ^ http://www.sciencemag.org/cgi/content/fu ll/288/5472/1819?maxtoshow=&HITS=10&hits =10&RESULTFORMAT=&fulltext=zag+morocco&s earchid=1129920472874_9236&stored_search =&FIRSTINDEX=0#RF2 (4.7 +- .2 billion years) 4. ^ sci has 4.7 +- .2 by where did 4.571 come from? |
[1] The ''Zag'' meteorite fell to Earth in 1988 COPYRIGHTED source: http://news.bbc.co.uk/1/hi/sci/t ech/783048.stm | |
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4,530,000,000 YBN | 33) Oldest Moon rock returned from Apollo missions (4.53 billions old). |
[1] http://www.nasm.si.edu/exhibitions/attm/ atmimages/S73-15446.f.jpg http://www.nasm.si.edu/exhibitions/attm/ nojs/wl.br.1.html source: | |
LIFE | |||
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4,500,000,000 YBN | 50) Start Precambrian Eon, Hadean Era.1 2 FOOTNOTES 1. ^ The geological Society of America ucmp.berkeley.edu 2. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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4,450,000,000 YBN | 21) Planet earth cools, molten rock cools into thin crust, H2O condenses from the atmosphere by raining, filling the lowest parts of land to make the first earth oceans, lakes, and rivers.1 FOOTNOTES 1. ^ part about rain and streams going to bottom of land: http://www.ersdac.or.jp/Others/geoessay_ htm/geoessay_e/geo_text_09_e.htm | ||
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4,404,000,000 YBN | 34) Oldest "terrestrial" (not from meteorite) zircon yet found on earth, 4.404 billion years old, from Gneiss in West Australia, is evidence that the crust and liquid water were on the surface of earth 4.4 billion years before now.1 FOOTNOTES 1. ^ http://www.nature.com/nature/links/01011 1/010111-1.html |
[1] http://www.geology.wisc.edu/zircon/Earli est%20Piece/Images/8.jpg source: | |
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4,400,000,000 YBN | 18) Amino acids, phosphates, and sugars, the components of living objects are created on earth. These molecules are made in the oceans, fresh water, and or atmosphere of earth (or other planets) by lightning, photons with ultraviolet frequency from the star, or ocean floor volcanos. | ||
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4,395,000,000 YBN | 19) How nucleic acids (polymers made of nucleotides), proteins (polymers made of amino acids), carbohydrates (polymers made of sugars) and lipids (glycerol attached to fatty acids) evolved is not clearly known. Some proteins and nucleic acids have been formed in labs by using clay which can dehydrate and which provides long linear crystal structures to build proteins and nucleic acids on. Amino acids join together to form polypeptides when an H2O molecule is formed from a Hydrogen (H) on 1 amino acid and a hydroxyl (OH) on the second. Are all proteins, carbohydrates, lipids and DNA the products of living objects? Is RNA the only molecule of these that was made without the help of living objects? The most popular theory now has RNA (and potentially lipids) evolving first before any living objects. There is still a large amount of experiment, exploration and education that needs to be done to understand the origins of living objects on planet earth. My opinion is that as soon as there was liquid water on the earth, 4.4 billion years before now, as zircon crystals show, the construction of living objects started on earth. | ||
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4,390,000,000 YBN | 25) RNA duplication evolves.
Perhaps RNA molecules, called "ribozymes" evolved which can make copies of RNA, by connecting free floating nucleotides that match a nucleotide on the same or a different RNA, without any proteins. But until such ribozyme RNA molecules are found, the only molecule known to copy nucleic acids are proteins called polymerases. If such ribozymes exist, then one of the first coded instructions on the RNA molecule that was the ancestor of every living species, must have been the code to make this ribozyme. | ||
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4,385,000,000 YBN | 167) Protein assembly evolves with the creation of various Transfer RNA (tRNA) molecules. Random mutations in the copying (and perhaps even in the natural formation) of RNA molecules probably created a number of the necessary tRNAs (transfer RNA, an RNA molecule responsible for matching free floating amino acid molecules to 3 nucleotide sequences on other RNA molecules). This would be a precellular protein assembly system, where tRNA (transfer RNA) molecules can build polypeptide chains of amino acids by linking directly to other RNA strands. Part of each tRNA molecule bonds with a specific amino acid, and a 3 nucleotide sequence from a different part of the tRNA molecule bonds with the opposite matching 3 nucleotide sequence on an (m)RNA molecule. Since there are tRNA molecules for each amino acid (although some tRNAs can attach to more than one amino acid?), there must have been a slow accumulation of various tRNA molecules for each of the 20 amino acids used in constructing polypeptides in cells living now. Perhaps after the evolution of the first tRNA, the first polypeptides were chains of all the same one amino acid. With the evolution of a second tRNA polypeptides would have more variety because now two amino acids would be available to build polypeptides. This polypeptide assembly system may exist freely in water, or within a liposome1 . This sytem builds many more proteins than would be built without such a system. The mRNA with the code to make copier RNA, now also contains the code to produce various tRNA molecules. These molecules function as a unit, and proto-cell, with the rest of the mRNA initially containing random codes for random proteins. For the first time, RNA code represents a template for other RNA molecules, but also a template for building proteins with the help of tRNA molecules. There is some question of where the origin of the first cell took place, near volcanos on the ocean floor, or in fresh water lakes and tidal pools near volcanos on land, because unprotected nucleic acids cannot exist for much time in the ocean because of Sodium and Chlorine. FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). supports liposome theory | ||
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4,380,000,000 YBN | 168) Ribosomal RNA (rRNA) evolves. Ribosomal RNA moves down mRNA molecules functioning as a platform for bringing the mRNA and tRNA molecules together to assemble polypeptides (proteins). This rRNA serves as an early ribosome; objects that serve as sites for building polypeptides and are found in every cell. As time continues the ribosome will grow to include two more RNA molecules, some protein molecules, and a second half that will make polypeptide construction more efficient. The rRNA serves the purpose of bringing amino acids close enough to bond with each other to form polypeptides. As an rRNA moves down an mRNA, tRNA molecules bond with the mRNA and on the opposite side of the tRNA, a matching amino acid (separates? from the tRNA and) attaches to a growing polypeptide chain. Now the mRNA that is the ancestral/progenitor of all of life, contains the code for the copier RNA, tRNAs, and the rRNA molecule. These nucleic acids function as a unit, and proto-cell. | ||
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4,375,000,000 YBN | 211) The first protein of real importance is built, an RNA polymerase. A molecule that can more efficiently copy RNA. | ||
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4,370,000,000 YBN | 41) A ribonucleotide reductase protein is built by the early ribosome protein making protocell. This protein changes ribonucleotides into deoxyribonucleotides. This allows the first DNA molecule on earth to be assembled. Ribonucleotide reductase may be the molecule that allowed DNA to be the template for the line of cells that survived to now. | ||
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4,365,000,000 YBN | 212) A DNA polymerase protein evolves to copy DNA by assembling DNA nucleotides from other DNA molecules. | ||
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4,360,000,000 YBN | 166) An RNA molecule evolves that causes the early ribosome to create reverse transcriptase, a protein that can assemble DNA molecules from an RNA molecule template. With this advance, a DNA molecule can be constructed that has all of the code that was stored on the long evolved RNA molecule. DNA now serves as a more stable template for making mRNA, each tRNA, rRNA, and the RNA and DNA polymerases. RNA polymerase proteins build RNA molecules using the new DNA template, that still perform their original polypeptide building function together with the tRNA and rRNA molecules, but are labeled "mRNA" (Messenger RNA) because they move from DNA to ribosome. | ||
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4,355,000,000 YBN | 20) The first cell membrane evolves around DNA, made of proteins. This membrane holds water inside a cell. This is the first cell. rRNA comparison shows that this is most likely a eubacterium.1 DNA produces instructions for cytoplasm, the cytoplasm is assembled from proteins made by the ribosome. For the first time, DNA and ribosomes are building cell structure. The templates for each tRNA, rRNA, mRNA and DNA polymerase proteins are already coded in a central strand of DNA. DNA protected by cytoplasm is more likely to survive and copy. This cell is heterotrophic and has no metabolism to produce ATP. Amino acids, nucleotides, H2O, and other molecules enter and exit the cytoplasm only because of a difference in concentration from inside and outside the cell (passive transport) and represent the beginnings of the first digestive system. This either happens in fresh water lakes or in salty oceans, perhaps near lava vents on or under the ocean floor. As this line of DNA continues to make copies of itself, all copies now have cytoplasm. The DNA is composed mainly of instructions to assemble the nucleic acids and proteins needed to build ribosomes, polymerases and cytoplasm. This cell structure forms the basis of all future cells of every living object on earth. These first cells are anaerobic (do not require free oxygen) and heterotrophic, meaning that they do not make their own food: amino acids, nucleotides, phosphates, and sugars. These bacteria depend on these molecules and photons in the form of heat to reproduce and grow. A system of division must evolve which attaches the original and newly synthesized copy of DNA to the cytoplasm, so that as the cell grows, the two copies of DNA can be separated and the first membraned cells can divide into two cells. This is the beginning of the "binary fission" method of cell division. Division of the cell begins with the division of the DNA membrane-attachment site and separates by the growth of new cytoplasm. FOOTNOTES 1. ^ source for eubacteria as oldest rRNA. Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989). p48 first step in prokaryote division is membrane-attachment site divides. prokaryote DNA attaches to cell membrane, and new membrane growth moves apart | ||
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4,350,000,001 YBN | 26) Perhaps DNA that is connected in a circle allows the DNA polymerase to make continuous copies of the cell. | ||
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4,345,000,000 YBN | 195) Proteins that actively transport molecules into and out of the cytoplasm (facilitative diffusion) evolve.1 FOOTN OTES 1. ^ http://www.cat.cc.md.us/~gkaiser/biotuto rials/eustruct/cmeu.html |
[1] Uniporters are transport proteins that transport a substance across a membrane down a concentration gradient from an area of greater concentration to lesser concentration. The transport is powered by the potential energy of a concentration gradient and does not require metabolic energy. source: http://www.cat.cc.md.us/~gkaiser /biotutorials/eustruct/cmeu.html
[2] Channel proteins transport water or certain ions down a concentration gradient from an area of higher concentration to an area of lower concentration. In the case of water, the channel proteins are called aquaporins. Water molecules are small enough that they can also pass between the phospholipids in the cytoplasmic membrane by passive diffusion. source: | |
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4,340,000,000 YBN | 23) The first viruses are made either from bacteria, or are initially bacteria. These cells depend on the DNA duplicating and protein producing systems of other cells to reproduce themselves. Over time, more effective, and efficient virus designs will survive.1 FOOTNOTES 1. ^ http://cellbio.utmb.edu/cellbio/rer2.htm | ||
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4,335,000,000 YBN | 28) Glycolysis evolves in the cytoplasm. Cells can now make ATP from glucose and eventually other monosaccharides, the end product is pyruvate. The glycolysis equation is: C6H12O6 (glucose) + 2 NAD+ + 2 ADP + 2 P -----> 2 pyruvic acid, (CH3(C=O)COOH + 2 ATP + 2 NADH + 2 H+ | ||
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4,330,000,000 YBN | 44) Fermentation evolves in the cytoplasm. Cells (all anaerobic) can now make more ATP and convert pyruvate (the final product of glycolysis) to lactate (an ionized form of lactic acid).1 FOOTNOTES 1. ^ http://216.239.63.104/search?q=cache:3s2 stckAJoMJ:www.nmc.edu/~ftank/115f04/Ch%2 5209%2520Notes.pdf+cellular+respiration+ oldest&hl=en | ||
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4,325,000,000 YBN | 213) A second kind of fermentation evolves in the cytoplasm. Cells (all anaerobic) can now convert pyruvate (the final product of glycolysis) to ethanol.1 FOOTNOTES 1. ^ http://216.239.63.104/search?q=cache:3s2 stckAJoMJ:www.nmc.edu/~ftank/115f04/Ch%2 5209%2520Notes.pdf+cellular+respiration+ oldest&hl=en | ||
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4,320,000,000 YBN 1 | 183) Cells evolve that make proteins that can assemble lipids. FOOTNOTES 1. ^ find biomarker evidence | ||
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4,315,000,000 YBN | 196) Cells that use both proteins and metabolism (ATP) to transport molecules into and out of the cytoplasm (active transport) evolve.1 FOOTNOTES 1. ^ http://www.cat.cc.md.us/~gkaiser/biotuto rials/eustruct/cmeu.html |
[1] TP: not clear what the red circles are, some kind of molecule I guess. Antiporters are transport proteins that simultaneously transport two substances across the membrane in opposite directions; one against the concentration gradient and one with the concentration gradient. Antiporters typically use proton motive force to transport a substrate across the membrane. The movement of protons across the membrane (proton motive force) provides the energy for transporting the substrate across the membrane against its concentration gradient.. source: http://www.cat.cc.md.us/~gkaiser /biotutorials/eustruct/cmeu.html
[2] Symporters are transport proteins that simultaneously transport two substances across the membrane in the same direction; one against the concentration gradient and one with the concentration gradient. Symporters often use proton motive force to transport a substrate across the membrane. The movement of protons across the membrane (proton motive force) provides the energy for transporting the substrate. source: | |
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4,310,000,000 YBN | 76) Pili, plasmids and conjugation evolves in prokaryotes. Now some prokaryotes can exchange circular pieces of DNA (plasmids), through tubes (pili). Conjugation may be the process that led to sex (cellular fusion) and also the transition from a circle of DNA to chromosomes in eukaryotes, since some protists (cilliates and some algae) reproduce sexually by conjugation.1 FOOTNOTES 1. ^ conjugation in protists, flagella in eukaryotes: Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989). |
[1] the fertility factor or F factor is a very large (94,500 bp) circular dsDNA plasmid; it is generally independent of the host chromosome. COPYRIGHTED source: http://www.mun.ca/biochem/course s/3107/images/Fplasmidmap.gif
[2] conjugation (via pilus) COPYRIGHTED EDU source: http://www.bio.miami.edu/dana/16 0/conjugation.jpg | |
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4,307,000,000 YBN | 292) Prokaryote flagella evolve.1 FOOTN OTES 1. ^ conjugation in protists, flagella in eukaryotes: Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989). | ||
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4,305,000,000 YBN | 64) Operons, sequences of DNA that allow certain proteins coded by DNA to not be built, evolve. Proteins bind with these DNA sequences to stop RNA polymerase from building mRNA molecules which would be translated into proteins. Operons allow a bacterium to produce certain proteins only when necessary. Bacteria before now can only build a constant stream of all proteins encoded in their DNA.1 2 FOOTN OTES 1. ^ http://info.bio.cmu.edu/Courses/03441/Te rmPapers/99TermPapers/GenEvo/operon.html 2. ^ http://web.indstate.edu/thcme/mwking/gen e-regulation.html#table | ||
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4,304,500,000 YBN | 322) Nitrogen fixation evolves in eubacteria. |
[1] This is an image of nitrogen cycle taken from this [1] EPA website. PD source: http://en.wikipedia.org/wiki/Ima ge:Nitrogen_Cycle.jpg | |
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4,304,000,000 YBN | 287) Multicellularity in the form of filment growth evolves in prokaryotes. | ||
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4,302,000,000 YBN 1 | 316) Cell differentiation in prokaryotes evolve. Heterocysts evolve in cyanobacteria. Heterocysts are specialized nitrogen-fixing cells formed by some filamentous cyanobacteria during nitrogen starvation. FOOTNOTES 1. ^ "Heterocyst". Wikipedia. Wikipedia, 2008. http://en.wikipedia.org/wiki/Heterocyst |
[1] Anabaena COPYRIGHTED EDU source: http://home.manhattan.edu/~franc es.cardillo/plants/monera/anabaena.gif
[2] Anabaena smitthi COPYRIGHTED FRANCE source: http://www.ac-rennes.fr/pedagogi e/svt/photo/microalg/anabaena.jpg | |
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4,300,000,000 YBN | 58) First autotrophic cells, cells that can produce some if not all of their own food (amino acids, nucleotides, sugars, phophates, lipids, and carbohydrates), but require phosphorus, nitrogen, CO2, water and light in the form of heat.1 There are only 2 kinds of autotrophy: Lithotrophy and Photosynthesis. These are lithotrophic cells that change inorganic (abiotic) molecules into organic molecules. These cells are archaebacteria, called methanogens that perform the reaction: 4H2 + CO2 -> CH4 + 2H2O. They convert CO2 into Methane. Methane is better than CO2 for trapping heat, and could have contributed to heating the earth. FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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4,295,000,000 YBN | 49) First photosynthetic cells. These cells only have Photosystem I. Photosynthesis Photosystem I evolves in early anaerobic prokaryote cells. One of two photosythesis systems, photosystem I uses a pigment chlorophyll A, absorbs photons in 700 nm wave lengths best, breaking the bond betwenn H2 and S. They are anaerobic and perform the reaction: H2S (Hydrogen Sulfide) + CO2 + light -> CH2O (Formaldehyde) + 2S. | ||
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4,290,000,000 YBN | 43) Photosynthesis Photosystem II evolves in early prokaryote cells. Photosystem 2 absorbs photons best at 680nm wavelengths, a higher frequency of light than Photosystem I. These cells can break the strong Hydrogen bonds between Hydrogen and Oxygen in water molecules (more abundant than Sulphur). This system emits free Oxygen.1 The simple equation of photosynthesis is: 6 H2O + 6 CO2 + photons = C6H12O6 (glucose) + 6O2. The detailed steps of photosynthesis are called the "Calvin Cycle". Prokaryote cells can now produce their own glucose to store and be converted to ATP by glycolysis and fermentation later. This sytem is the main system responsible for producing the Oxygen now in the air of earth. FOOTNOTES 1. ^ http://www.emc.maricopa.edu/faculty/fara bee/BIOBK/BioBookPS.htmlhttp://www.ebi.a c.uk/interpro/potm/2004_11/Page1.htm3 | ||
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4,280,000,000 YBN 2 | 57) Cellular Respiration (also called the "Citric Acid Cycle", and the "Krebs Cycle") evolves, probably in cyanobacteria, as a substitute for fermentaton, by using oxygen to break down the products of glycolysis, pyruvic acid, to CO2 and H2O, producing 18 more ATP molecules.1 This is the first aerobic cell, a cell that has an oxygen based metabolism. This cell uses oxygen to convert glucose (and eventually other sugars and fats) into CO2, H2O and ATP. For example, cells that oxidize glucose perform the reaction: C6H12O6 + 6 O2 + 38 ADP + 38 phosphate -> 6 CO2 + 6 H2O + 38 ATP This reaction (with glycolysis) can produce up to 36 ATP molecules. Cellular respiration is the opposite (although the specific reactions differ) of photosynthesis which starts with H2O and CO2 and produces glucose. FOOTNOTES 1. ^ "Aerobic organism". Wikipedia. Wikipedia, 2008. http://en.wikipedia.org/wiki/Aerobic_org anism 2. ^ Ted Huntington,. my own guess based on absence of published information |
[1] kreb cycle from http://people.unt.edu/~hds0006/tca/ source: | |
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4,250,000,000 YBN 8 9 10 11 12 13 14 | 77) There are many widely varying estimates of when the first Eubacteria and Archaea evolved. Eubacteria and Archaea (also called Archaebacteria) are the two major lines of Prokaryotes. Prokaryotes are the most primitive living objects ever found. In contrast to the later evolved Eukaryotes, Prokaryotes have a circle of DNA located in their cytoplasm (not chromosomes) and have no nucleus. At least one genetic comparison shows Eubacteria and Archaea evolving now.1 2 3 4 5 6 7 After the full genomes of all living species are known, and understood we will have more certainty about the history of evolution. Many genetic trees are based on DNA genes (sequences of DNA that define nucleic acids or proteins). In particular the genes for ribosomal RNA are thought to be very conserved over time, although perhaps genes for reproduction, or cytoplasm, for example may later prove to be more conserved over time. FOOTNOTES 1. ^ http://www.nature.com/nrg/journal/v3/n11 /full/nrg929_fs.html 2. ^ Russell F. Doolittle, Da-Fei Feng, Simon Tsang, Glen Cho, Elizabeth Little, "Determining Divergence Times of the Major Kingdoms of Living Organisms with a Protein Clock", Science, (1996). 2142-1873my 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2300my 4. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 4100my (has arche b4 eu) 5. ^ Osawa, S., Honjo, "Archaebacteria vs Metabacteria : Phylogenetic tree of organisms indicated by comparison of 5S ribosomal RNA sequences.", (Tokyo: Springer, Tokyo/ Berlin eds.:"Evolution of Life", pp. 325-336,, 1991). 1800my 6. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 4000my 7. ^ S. Blair Hedges and Sudhir Kumar, "Genomic clocks and evolutionary timescales", Trends in Genetics Volume 19, Issue 4 , April 2003, Pages 200-206, (2003). 3970my 8. ^ http://www.nature.com/nrg/journal/v3/n11 /full/nrg929_fs.html 9. ^ Russell F. Doolittle, Da-Fei Feng, Simon Tsang, Glen Cho, Elizabeth Little, "Determining Divergence Times of the Major Kingdoms of Living Organisms with a Protein Clock", Science, (1996). 2142-1873my (2142-1873my) 10. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2300my (2300my) 11. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 4100my (has arche b4 eu) (4100my) 12. ^ Osawa, S., Honjo, "Archaebacteria vs Metabacteria : Phylogenetic tree of organisms indicated by comparison of 5S ribosomal RNA sequences.", (Tokyo: Springer, Tokyo/ Berlin eds.:"Evolution of Life", pp. 325-336,, 1991). 1800my (1800my) 13. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849 (2002); doi:10.1038/nrg929, (2002). 4000my (4000my) 14. ^ S. Blair Hedges and Sudhir Kumar, "Genomic clocks and evolutionary timescales", Trends in Genetics Volume 19, Issue 4 , April 2003, Pages 200-206, (2003). 3970my (3970my) |
[1] Figure 1) Changing views of the tree and timescale of life. a) An early-1990s view, with the tree determined mostly from ribosomal RNA (rRNA) sequence analysis. This tree emphasizes vertical (as opposed to horizontal) evolution and the close relationship between eukaryotes and the Archaebacteria. The deep branching (>3.5 Giga (109) years ago, Gya) of CYANOBACTERIA (Cy) and other Eubacteria (purple), the shallow branching (approx1 Gya) of plants (Pl), animals (An) and fungi (Fu), and the early origin of mitochondria (Mi), were based on interpretations of the geochemical and fossil record7, 8. Some deeply branching amitochondriate (Am) species were believed to have arisen before the origin of mitochondria44. Major symbiotic events (black dots) were introduced to explain the origin of eukaryotic organelles42, but were not assumed to be associated with large transfers of genes to the host nucleus. They were: Eu, joining of an archaebacterium host with a eubacterium (presumably a SPIROCHAETE) to produce an amitochondriate eukaryote; Mi, joining of a eukaryote host with an alpha-proteobacterium (Ap) symbiont, leading to the origin of mitochondria, and plastids (Ps), joining of a eukaryote host with a cyanobacterium symbiont, forming the origin of plastids on the plant lineage and possibly on other lineages. b) The present view, based on extensive genomic analysis. Eukaryotes are no longer considered to be close relatives of Archaebacteria, but are genomic hybrids of Archaebacteria and Eubacteria, owing to the transfer of large numbers of genes from the symbiont genome to the nucleus of the host (indicated by coloured arrows). Other new features, largely derived from molecular-clock studies16, 39 (Box 1), include a relatively recent origin of Cyanobacteria (approx2.6 Gya) and mitochondria (approx1.8 Gya), an early origin (approx1.5 Gya) of plants, animals and fungi, and a close relationship between animals and fungi. Coloured dashed lines indicate controversial aspects of the present view: the existence of a premitochondrial symbiotic event and of living amitochondriate eukaryotes, ancestors of which never had mitochondria. c) The times of divergence of selected model organisms from humans, based on molecular clocks. For the prokaryotes (red), because of different possible origins through symbiotic events, divergence times depend on the gene of interest. source: http://www.nature.com/nrg/journa l/v3/n11/full/nrg929_fs.html
[2] Figure 2 A phylogeny of prokaryotes. The relationships of selected prokaryote model organisms based on recent studies14-19. Times of divergence (million years ago (Mya) plusminus one standard error) are indicated at nodes in the tree16, 39. Branch lengths are not proportional to time. Phyla and phylum-level groupings are indicated on the right. source: http://www.nature.com/nrg/journa l/v3/n11/full/nrg929_fs.html | |
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4,112,000,000 YBN 4 | 180) The Archaea Phylum, Euryarchaeotes evolve.1 2 3 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ nature v417 n6886 3. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 4. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). |
[1] tree of archaebacteria (archaea) COPYRIGHTED source: http://www.uni-giessen.de/~gf126 5/GROUPS/KLUG/Stammbaum.html
[2] A phylogenetic tree of living things, based on RNA data, showing the separation of bacteria, archaea, and eukaryotes. Trees constructed with other genes are generally similar, although they may place some early-branching groups very differently, thanks to long branch attraction. The exact relationships of the three domains are still being debated, as is the position of the root of the tree. It has also been suggested that due to lateral gene transfer, a tree may not be the best representation of the genetic relationships of all organisms. NASA source: http://en.wikipedia.org/wiki/Ima ge:PhylogeneticTree.jpg | |
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4,112,000,000 YBN 4 | 181) The Archaea Phylum, Crenarchaeotes evolves.1 2 3 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ nature v417 n6886 3. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 4. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). |
[1] tree of archaea ? source: http://www.uni-giessen.de/~gf126 5/GROUPS/KLUG/Stammbaum.html
[2] Microscopia elettronica a scansione dell'archeobatterio termoacidofilo Sulfolobus solfataricus COPYRIGHT ITALY source: http://www.area.fi.cnr.it/r&f/n6 /ingrand.htm | |
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3,977,000,000 YBN 3 | 193) Eubacteria "Hyperthermophiles" (Aquifex, Thermotoga, etc.) evolve now.1 2 FOOTNOTES 1. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 2. ^ Brocks, Buick, "A reconstruction of Archean biological diversity based on", Geochimica et cosmochimica acta, (2003). 3. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). |
[1] Aquifex pyrophilus (platinum shadowed). © K.O. Stetter & Reinhard Rachel, University of Regensburg. source: http://biology.kenyon.edu/Microb ial_Biorealm/bacteria/aquifex/aquifex.ht m
[2] Aquifex aeolicus. © K.O. Stetter & Reinhard Rachel, University of Regensburg. source: http://biology.kenyon.edu/Microb ial_Biorealm/bacteria/aquifex/aquifex.ht m | |
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3,850,000,000 YBN | 36) The oldest sediment on earth is also the oldest Banded Iron Formation, on Akilia Island in Western Greenland. The oldest evidence for life on earth was found in this rock by measuring the ratio of carbon 12 to carbon 13 in grains of apatite (calcium phosphate) from this rock. Life uses the lighter Carbon-12 isotope and not Carbon-13 and so the ratio of carbon-12 to carbon-13 is different from a nonliving source (calcium carbonate or limestone).1 2 FO OTNOTES 1. ^ Mojzsis, et al. nature nov 7, 1996 http://www.nature.com/cgi-taf/DynaPage.t af?file=/nature/journal/v384/n6604/index .html, 2:102, 2. ^ http://jersey.uoregon.edu/~mstrick/Rogue ComCollege/RCC_Lectures/Banded_Iron.html |
source: nature 11/7/96 | |
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3,850,000,000 YBN | 45) This marks the beginning of the Banded Iron Formation Rocks. These rocks are sedimentary. They are made of iron rich chert (silicates, like SiO2). These rocks have alternative bands of orange or yellow and black. In the red parts the iron is oxydized (contains iron oxides, either hematite {Fe2O3 = rust} or magnetite {Fe3O4]}).1 2 3 4 5 These bands may have formed because photosynthetic bacteria (in stromatolites found in shallow ocean shores, and purple bacteria floating in water) produce oxygen from CO2 during photosynthesis. When the level of oxygen in the water became too high, many bacteria died, and this cycle created the BIF. But BIF also may form naturally when photons in uv frequencies split H2O into H2 and O2. So perhaps the BIF bands represent cycles of more or less uv light reaching the earth. Perhaps the alternating phenomenon is similar to eukaryotic algal blooms. In any event, this free oxygen bonded with the many tons of iron dissolved in the water to form insoluable iron oxide which then fell to the ocean floor to form the orange layers of Banded Iron Formation. How these alternating bands are made is not clear and has not yet been duplicated in a lab. This cycle of alternating orange and black bands will continue for 2 billion years until 1,800 million years before now. This is the beginning of oxygen production on earth, the atmosphere of earth still has only small amounts of oxygen at this time. FOOTNOTES 1. ^ Roger Lewin, "Thread of Life", (New York: Smithsonian Books, 1982). p102 2. ^ http://jersey.uoregon.edu/~mstrick/Rogue ComCollege/RCC_Lectures/Banded_Iron.html 3. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 4. ^ "Banded iron formation". Wikipedia. Wikipedia, 2008. http://en.wikipedia.org/wiki/Banded_iron _formation |
source: nature 11/7/96 | |
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3,800,000,000 YBN | 51) End Hadean Era, start Archean Era.1 2 FOOTNOTES 1. ^ The geological Society of America ucmp.berkeley.edu 2. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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3,800,000,000 YBN 3 | 185) Isoprene compounds from Isua, Greenland Banded Iron Formation sediment are evidence of the existence of Archaea.1 2 FOOTNOTES 1. ^ http://www.ucmp.berkeley.edu/archaea/arc haeafr.html 2. ^ Jürgen Hahn & Pat Haug. 1986. Traces of Archaebacteria in ancient sediments. System. Appl. Microbiol. 7: 178-183. (Archaebacteria '85 Proceedings). 3. ^ http://www.ucmp.berkeley.edu/archaea/arc haeafr.html | ||
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3,760,000,000 YBN 2 | 186) Sulfur isotope ratios (34S/32S) and Hydrocarbon molecules (alkanes) detected in 3760 billion year old Isua Banded Iron Formation, indicate the possibility of photosynthetic sulfate reducing bacteria (Archaea, for example Sulpholobus) and Cyanobacteria living at that time.1 FOOTNOTES 1. ^ Systematic and Applied Microbiology, Vol 7, pp 178-183 1986 2. ^ Systematic and Applied Microbiology, Vol 7, pp 180-189 1986 | ||
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3,700,000,000 YBN 2 | 184) Amount of Uranium isotope measured in Isua, Greenland Banded Iron Formation evidence of prokaryote Oxygen photosynthesis.1 FOOTNOTES 1. ^ Earth and Planetary Science Letters Volume 217, Issues 3-4 , 15 January 2004, Pages 237-244U-rich "Archaean sea-floor sediments from Greenland - indications of >3700 Ma oxygenic photosynthesis" Minik T. Rosing and Robert Frei 2. ^ Earth and Planetary Science Letters Volume 217, Issues 3-4 , 15 January 2004, Pages 237-244U-rich "Archaean sea-floor sediments from Greenland - indications of >3700 Ma oxygenic photosynthesis" Minik T. Rosing and Robert Frei | ||
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3,500,000,000 YBN | 37) The oldest fossil evidence of life yet found. Stromatolites made by photosynthetic bacteria found in both Warrawoona, Western Australia, and Fig Tree Group, South Africa.1 2 FOOTNOTES 1. ^ nature feb 6, 1986 2. ^ nature apr 3, 1980 |
[1] image on left is from swaziland source: nature feb 6
source: 1986 | |
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3,500,000,000 YBN | 39) Oldest fossils of an organism, thought to be cyanobacteria, found in 3,500 Million Year old chert from South Africa and 3,465 Million year old Apex chert of north-western Australia.1 2 3 4 5 FOOTNOTES 1. ^ warrawoona Nature416, 73 - 76 (07 Mar 2002) Letters to Nature http://www.nature.com/nature/journal/v 416/n6876/full/416073a_fs.html 2. ^ swaziland Nature 314, 530-532 (11 Apr 1985) Letters to Editor "Filamentous microfossils from the 3,500-Myr-old Onverwacht Group, Barberton Mountain Land, South Africa" 3. ^ argues that these are not fossils: http://www.nature.com/nature/j ournal/v420/n6915/full/420476b.html "we contend that the Raman spectra of Schopf et al.1 indicate that these are disordered carbonaceous materials of indeterminate origin. We maintain that Raman spectroscopy cannot be used to identify microfossils unambiguously, although it is a useful technique for pinpointing promising microscopic entities for further investigation." 4. ^ http://www.nature.com/news/2002/020304/f ull/020304-6.html "Gloves are coming off in ancient bacteria bust-up." 2002 5. ^ http://www.nature.com/nature/journal/v41 6/n6876/full/416076a.html braiser et al. "Questioning the evidence for Earth's oldest fossils" |
[1] Figure 1 Optical photomicrographs showing carbonaceous (kerogenous) filamentous microbial fossils in petrographic thin sections of Precambrian cherts. Scale in a represents images in a and c-i; scale in b represents image in b. All parts show photomontages, which is necessitated by the three-dimensional preservation of the cylindrical sinuous permineralized microbes. Squares in each part indicate the areas for which chemical data are presented in Figs 2 and 3. a, An unnamed cylindrical prokaryotic filament, probably the degraded cellular trichome or tubular sheath of an oscillatoriacean cyanobacterium, from the 770-Myr Skillogalee Dolomite of South Australia12. b, Gunflintia grandis, a cellular probably oscillatoriacean trichome, from the 2,100-Myr Gunflint Formation of Ontario, Canada13. c, d, Unnamed highly carbonized filamentous prokaryotes from the 3,375-Myr Kromberg Formation of South Africa14: the poorly preserved cylindrical trichome of a noncyanobacterial or oscillatoriacean prokaryote (c); the disrupted, originally cellular trichomic remnants possibly of an Oscillatoria- or Lyngbya-like cyanobacterium (d). e-i, Cellular microbial filaments from the 3,465-Myr Apex chert of northwestern Western Australia: Primaevifilum amoenum4,5, from the collections of The Natural History Museum (TNHM), London, specimen V.63164[6] (e); P. amoenum4 (f); the holotype of P. delicatulum4,5,15, TNHM V.63165[2] (g); P. conicoterminatum5, TNHM V63164[9] (h); the holotype of Eoleptonema apex5, TNHM V.63729[1] (i). source: Nature416
[2] Fig. 3 Filamentous microfossils: a, cylindrical microfossil from Hooggenoeg sample; b, threadlike and tubular filaments extending between laminae, Kromberg sample; c,d,e, tubular filamnets oriented subparallel to bedding, Kromberg sample; f, threadlike filament flattened parallel to bedding, Kromberg sample. source: 73 - 76 (07 Mar 2002) Letters to Nature http://www.nature.com/nature/journal/v41 6/n6876/fig_tab/416073a_F1.html | |
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3,470,000,000 YBN 2 | 182) Sulphate fossil molecular marker evidence of moderate thermophile sulphur reducing prokaryotes from North Pole, Australia.1 FOOTNOTES 1. ^ http://www.nature.com/cgi-taf/DynaPage.t af?file=/nature/journal/v410/n6824/full/ 410077a0_fs.html 2. ^ http://www.nature.com/cgi-taf/DynaPage.t af?file=/nature/journal/v410/n6824/full/ 410077a0_fs.html |
[1] get larger image source: file:///root/web/fossils_biomark er_science_v67_i22_nov_15_2003.html#bib9 9 | |
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3,470,000,000 YBN 2 | 216) Evidence of sulphate reduction by bacteria.1 FOOTNOTES 1. ^ http://www.nature.com/nature/journal/v41 0/n6824/full/410077a0.html 2. ^ http://www.nature.com/nature/journal/v41 0/n6824/full/410077a0.html |
[1] The tree is modified from ref. 2, and abstracted from phylogenetic trees presented in refs 26 and 27. The time calibration points are from ref. 30, with our additional constraint of 3.47 Gyr placed in the Bacterial domain. Lineages housing sulphate-reducers metabolizing at temperatures > 70 °C are shown by broken black lines, while lineages supporting sulphate-reducers metabolizing at < 70 °C are shown by heavy black lines. source: http://www.nature.com/nature/jou rnal/v410/n6824/fig_tab/410077a0_F4.html | |
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3,416,000,000 YBN 2 | 218) Fossil and molecular evidence of photosynthetic, probably anoxygenic, bacteria that lived in mats in the ocean date to this time.1 FOOTNOTES 1. ^ http://www.nature.com/nature/journal/v43 1/n7008/full/nature02888.html 2. ^ http://www.nature.com/nature/journal/v43 1/n7008/full/nature02888.html |
[1] a, Dark carbonaceous laminations draping an underlying coarse detrital carbonaceous grain (a), showing internal anastomosing and draping character (b) and, at the top (c) draping irregularities in underlying carbonaceous laminations. b, Dark carbonaceous laminations that have been eroded and rolled up by currents. c, Bundled filaments in the rolled laminations in b [tp: they should have clearly indicated that they are saying that these filaments are bacteria]. source: http://www.nature.com/nature/jou rnal/v431/n7008/fig_tab/nature02888_F4.h tml | |
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3,260,000,000 YBN 1 | 71) Budding evolves in prokayotes. Different from binary division, where a cell is split in half, in budding, a new complete cell is made in the original cell, and the new cell bursts through the cell wall, the original cell wall must then be repaired. FOOTNOTES 1. ^ Record ID 191. "Universe, life, Science Future". Ted Huntington. (based on my own estimate based on fossils from id191) (3.4) |
[1] Evolutionary relationships of model organisms and bacteria that show unusual reproductive strategies. This phylogenetic tree (a) illustrates the diversity of organisms that use the alternative reproductive strategies shown in (b). Bold type indicates complete or ongoing genome projects. Intracellular offspring are produced by several low-GC Gram-positive bacteria such as Metabacterium polyspora, Epulopiscium spp. and the segmented filamentous bacteria (SFB). Budding and multiple fission are found in the proteobacterial genera Hyphomonas and Bdellovibrio, respectively. In the case of the Cyanobacteria, Stanieria produces baeocytes and Chamaesiphon produces offspring by budding. Actinoplanes produce dispersible offspring by multiple fission of filaments within the sporangium. source: http://www.nature.com/nrmicro/jo urnal/v3/n3/full/nrmicro1096_fs.html (Nature Reviews Microbiology 3 [2] Electron micrograph of a Pirellula bacterium from giant tiger prawn tissue (Penaeus monodon). Notice the large crateriform structures (C) on the cell surface and flagella. From Fuerst et al. source: 214-224 (2005); doi:10.1038/nrmicro1096) | |
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3,250,000,000 YBN | 191) Fossils from Swartkoppie chert, South Africa are oldest evidence of procaryotes that reproduce by budding and not binary fission.1 FOOTNOTES 1. ^ http://www.sciencedirect.com/science?_ob =ArticleURL&_udi=B6VBP-42G6M5T-7&_user=4 422&_coverDate=02%2F01%2F2001&_fmt=full& _orig=browse&_cdi=5932&view=c&_acct=C000 059600&_version=1&_urlVersion=0&_userid= 4422&md5=d61bf36f008d6b2cba3ba5dbd5a628d 7&ref=full#bib9 MORE INFO [1] (maybe evidence): ZENTRALBLATT FUR BAKTERIOLOGIE MIKROBIOLOGIE UND HYGIENE I ABTEILUNG Pflug, H.D., 1982. Early diversification of life in the Archean. Zbl. Bakt. Hyg. I.Abt. Orig. C3, pp. 53-64.? |
[1] Fig. 4. (a-d) Organic microstructures from Swartkoppie chert, South Africa (ca 3.25 Ga). TEM-micrographs of demineralized specimen (a,b) Laser mass spectra (negative ions) from clusters of similar specimens. Field of measurement ca 1 small mu, Greekm diameter. (c,d) TEM-micrographs from demineralized Thin section. (e) Recent budding iron bacterium Pedomicrobium sp. (Fig. e from Ghiorse and Hirsch, 1979). source: http://www.sciencedirect.com/sci ence?_ob=MiamiCaptionURL&_method=retriev e&_udi=B6VBP-42G6M5T-7&_image=fig6&_ba=6 &_user=4422&_coverDate=02%2F01%2F2001&_f mt=full&_orig=browse&_cdi=5932&view=c&_a cct=C000059600&_version=1&_urlVersion=0& _userid=4422&md5=801178ddb930bd041063bae 7a3e0e204 | |
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3,235,000,000 YBN | 68) Thermophilic prokaryote fossils found in 3235 million year old deep-sea volcanogenic massive sulphide deposits from the Pilbara Craton of Australia may be oldest Archaea fossils.1 FOOTNOT ES 1. ^ Nature 405, 676 - 679 (08 June 2000); doi:10.1038/35015063 Filamentous microfossils in a 3,235-million-year-old volcanogenic massive sulphide deposit BIRGER RASMUSSEN |
[1] Photomicrographs of filaments from the Sulphur Springs VMS deposit. Scale bar, 10 µm. a-f, Straight, sinuous and curved morphologies, some densely intertwined. g, Filaments parallel to the concentric layering. h, Filaments oriented sub-perpendicular to banding. source: | |
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2,923,000,000 YBN 4 | 178) Eubacteria Phylum Firmicutes (low G+C {Guanine and Cytosine count} Gram positive) evolve.1 2 3 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Nature v417 n6886 (not TOL) 3. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 4. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). MORE INFO [1] http://en.wikipedia.org/wiki/Peptidoglyc an [2] firmicutes only bacteria to make endospores http://en.wikipedia.org/wiki/Endospore [3] http://en.wikipedia.org/wiki/Firmicutes |
[1] Listeria monocytogenes is a Gram-positive bacterium, in the division Firmicutes, named for Joseph Lister. It is motile by means of flagella. Some studies suggest that 1 to 10% of humans may carry L. monocytogenes in their intestines. Researchers have found L. monocytogenes in at least 37 mammalian species, both domesticated and feral, as well as in at least 17 species of birds and possibly in some species of fish and shellfish. Laboratories can isolate L. monocytogenes from soil, silage, and other environmental sources. L. monocytogenes is quite hardy and resists the deleterious effects of freezing, drying, and heat remarkably well for a bacterium that does not form spores. Most L. monocytogenes are pathogenic to some degree. source: http://en.wikipedia.org/wiki/Ima ge:Listeria.jpg
[2] These are bacteria (about 0.3 µm in diameter) that do not have outer walls, only cytoplasmic membranes. However, they do have cytoskeletal elements that give them a distinct non-spherical shape. They look like schmoos that are pulled along by their heads. How they are able to glide is a mystery. source: http://webmac.rowland.org/labs/b acteria/projects_glide.html | |
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2,800,000,000 YBN 5 | 177) Genetic comparison shows the ancestor of all Proteobacteria (Rickettsia {mitochondria}, gonorrhoea, Salmonella, E coli) evolving now.1 2 3 4 FOOTNOTES 1. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Tree of life, http://tolweb.org/tree/ 4. ^ David moreira, Purificacion Lopez-Garcia, "Symbiosis Between methanogenic Archaea and delta-Proteobacteria as the Origin of Eukaryotes: The Synthreophic Hypothesis", J Mol Evol (1998) 47:517-530. eukorig6_jmol.pdf 5. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). MORE INFO [1] multicellularity. http://www.mansfield.ohio-state.edu/~sab edon/biol3018.htm multicellularity. Multicellularity.pdf http://en.wikipedia.org/wiki/Escherichia _coli http://en.wikipedia.org/wiki/Proteobacte ria |
[1] Figure 1. Transmission electron micrograph of the ELB agent in XTC-2 cells. The rickettsia are free in the cytoplasm and surrounded by an electron transparent halo. Original magnification X 30,000. CDC PD source: www.cdc.gov/ncidod/ eid/vol7no1/raoultG1.htm
[2] Caulobacter crescentus. From http://sunflower.bio.indiana.edu/~ybrun/ L305.html COPYRIGHTED EDU was in wiki but appears to be removed source: http://upload.wikimedia.org/wiki pedia/en/4/42/Caulobacter.jpg | |
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2,784,000,000 YBN 2 | 176) Genetic comparison shows Eubacteria Phylum, Planctomycetes (Planctobacteria) evolving now.1 FOOTNO TES 1. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 2. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). MORE INFO [1] s10 http://ijs.sgmjournals.org/cgi/reprint/5 0/6/1965 [2] http://genomebiology.com/2002/3/6/resear ch/0031 [3] http://en.wikipedia.org/wiki/Planctomyce tes |
[1] Electron micrographs of cells of new Gemmata-like and Isosphaera-like isolates. (A) Negatively stained cell of the Gemmata-like strain JW11-2f5 showing crateriform structures (arrowhead) and coccoid cell morphology. Bar marker, 200 nm. (B) Negatively stained budding cell of Isosphaera-like strain CJuql1 showing uniform crateriform structures (arrowhead) on the mother cell and coccoid cell morphology. Bar marker, 200 nm. (C) Thin section of Gemmata-like cryosubstituted cell of strain JW3-8s0 showing the double-membrane-bounded nuclear body (NB) and nucleoid (N) enclosed within it. Bar marker, 200 nm. (D) Thin section of Isosphaera-like strain C2-3 possessing a fibrillar nucleoid (N) within a cytoplasmic compartment bounded by a single membrane (M) only. Bar marker, 200 nm. Appl Environ Microbiol. 2002 January; 68(1): 417-422. doi: 10.1128/AEM.68.1.417-422.2002. source: http://www.pubmedcentral.gov/art iclerender.fcgi?tool=pubmed&pubmedid=117 72655
[2] Evolutionary distance tree derived from comparative analysis of 16S rDNAs from freshwater and soil isolates and reference strains of the order Planctomycetales. Database accession numbers are shown in parentheses after species, strain, or clone names. Bootstrap values of greater than 70% from 100 bootstrap resamplings from the distance analysis are presented at nodes. Thermotoga maritima was used as an outgroup. Isolates from this study and representative named species of the planctomycetes are indicated in bold. The scale bar represents 0.1 nucleotide substitution per nucleotide position. Appl Environ Microbiol. 2002 January; 68(1): 417-422. doi: 10.1128/AEM.68.1.417-422.2002. source: http://florey.biosci.uq.edu.au/m ypa/images/fuerst2.gif | |
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2,784,000,000 YBN 6 | 179) Genetic comparison shows Eubacteria Phylum, Actinobacteria (high G+C, Gram positive) evolving now.1 2 3 4 5 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Nature v417 n6886, not TOL 3. ^ "Actinobacteria". Wikipedia. Wikipedia, 2008. http://en.wikipedia.org/wiki/Actinobacte ria 4. ^ http://asylumeclectica.com/malady/archiv es/leprosy.htm 5. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 6. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). |
[1] Frankia is a genus of nitrogen-fixing soil bacteria, which possesses a set of features that are unique amongst symbiotic nitrogen-fixing microorganisms, including rhizobia, making it an attractive taxon to study. These heterotrophic Gram-positive bacteria which are able to induce symbiotic nitrogen-fixing root nodules (actinorhizas) in a wide range of dicotyledonous species (actinorhizal plants), have also the capacity to fix atmospheric nitrogen in culture and under aerobic conditions. source: http://www.ibmc.up.pt/webpagesgr upos/cam/Frankia.htm
[2] Aerial mycelium and spore of Streptomyces coelicolor. The mycelium and the oval spores are about 1µm wide, typical for bacteria and much smaller than fungal hyphae and spores. (Scanning electron micrograph, Mark Buttner, Kim Findlay, John Innes Centre). COPYRIGHT UK source: http://www.sanger.ac.uk/Projects /S_coelicolor/micro_image4.shtml | |
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2,775,000,000 YBN 2 | 174) Genetic comparison shows Eubacteria Phylum, Spirochaetes (Syphilis, Lyme disease) evolving now.1 FOOTNOTES 1. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 2. ^ estimated from Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). MORE INFO [1] Tree of Life. http://tolweb.org/tree/ [2] Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). |
[1] Syphilis is a complex, sexually transmitted disease (STD) with a highly variable clinical course. The disease is caused by the bacterium, Treponema pallidum. In the United States, 32,871 cases of syphilis, including 432 cases of congenital syphilis, were detected by public health officials in 2002. Eight of the ten states with the highest rates of syphilis are located in the southern region of the United States. source: http://www.cdc.gov/nchstp/od/tus kegee/syphilis.htm
[2] leptospirose 200x magnified with dark-field microscope photo taken by bluuurgh at the dutch royal tropical institute (www.kit.nl) PD source: http://uhavax.hartford.edu/bugl/ images/Treponema%20pallidum.jpg | |
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2,775,000,000 YBN 3 4 | 175) Genetic comparison shows Eubacteria Phyla Bacteroidetes and Chlorobi (green sulphur bacteria) evolving now.1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004).. ^ 3. ^ estimate from Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 4. ^ estimate from Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). MORE INFO [1] Tree of Life [2] http://en.wikipedia.org/wiki/Bacteroidet es [3] http://en.wikipedia.org/wiki/Chlorobi |
[1] Bacteroides fragilis . From the Zdravotni University source: http://biology.kenyon.edu/Microb ial_Biorealm/bacteria/bacteroidete_chlor ob_group/bacteroides/bacteroides.htm
[2] Cross section of a Bacteroides showing an outer membrane, a peptidoglycan layer, and a cytoplasmic membrane. From New-asthma source: http://phil.cdc.gov/phil/details .asp | |
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2,775,000,000 YBN 2 | 217) Genetic comparison shows Eubacteria Phyla Chlamydiae and Verrucomicrobia evolving now.1 FOOTNOTE S 1. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 2. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). MORE INFO [1] Tree of Life. http://tolweb.org/tree/ [2] Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). [3] http://en.wikipedia.org/wiki/Chlamydiae [4] http://en.wikipedia.org/wiki/Verrucomicr obia |
[1] Chlamydia trachomatis wiki, is copyrighted source: http://en.wikipedia.org/wiki/Chl amydia_trachomatis
[2] wiki, public domain source: http://en.wikipedia.org/wiki/Ima ge:Chlamydophila_pneumoniae.jpg | |
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2,760,000,000 YBN 1 | 80) Endocytosis, a process where the cell membrane folds around some molecules to form a spherical vesicle which enters the cytoplasm, and exocytosis, the opposite process, where a vesicle combines with a call membrane to empty molecules outside a cell both evolve in an early eukaryote cell. Eukaryote cells can now swallow bacteria (phagocytosis) and liquid (pinocytosis). The cells can then (heterotrophically) use the molecules injested (for example a bacterium) for copying and to make ATP. This is the first time one cell can eat a different living cell. FOOTNOTES 1. ^ guess based on Cav-Smith saving endo before cytoskeleton |
[1] Pinocytosis In the process of pinocytosis the plasma membrane froms an invagination. What ever substance is found within the area of invagination is brought into the cell. In general this material will be dissolved in water and thus this process is also refered to as ''cellular drinking'' to indicate that liquids and material dissolved in liquids are ingested by the cell. This is opposed to the ingestion of large particulate material like bacteria or other cells or cell debris. source: http://academic.brooklyn.cuny.ed u/biology/bio4fv/page/endocytb.htm | |
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2,750,000,000 YBN 4 | 207) Cytoskeleton evolves in eukaryote cytoplasm.1 2 3 FOOTNOTES 1. ^ Cavalier-Smith, annals of Botony 2005 vol95 issue 1 2. ^ Margulis, L. 1998. Symbiotic Planet: A New Look at Evolution. Science Masters: Brockman Inc, New York. Margulis, L., Dolan, M., Guerrero, R. 2000. The Chimaeric eukaryote: Origin of the nucleus from the karyomastigont in amitochondriate protists. Colloquium. 97: 6954-6959. 3. ^ Symbiosis in cell evolution : microbial communities in the Archean and Proterozoic eons / Lynn Margulis. 1993 second edition 4. ^ guess based on ER and golgi made of same materia as cytoskeleton | ||
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2,725,000,000 YBN 11 | 60) First eukaryotic cell evolves.1 2 3 4 5 6 7 8 9 10 This cell has a nucleus, with either single strands or a circle of DNA inside. This is a single anaerobic cell. This is the first protist. This cell evolves either by: 1) two or more bacteria joined, one with flagella (perhaps a eubacteria) formed the nucleus, a second formed the cytoplasm outside the nucleus, eventually the code to build the entire cell including the instructions to build the symbiotic captured bacteria was included in the new nucleus, 2) the nucleus formed as part of the cytoplasm lattice, perhaps the outer wall folded in on itself creating a double membrane, or a membrane grew around the DNA (for example like planctobacteria) which provided more protection for the DNA from the movement and digestive activities of cytoplasm now without a rigid cell wall, 3) a bacteria with flagella that grew cytoplasm and a secondary cell wall outside the original cell wall, 4) a virus, 5) a DNA strand from conjugation with a different prokaryote stored in a vesicle. There are key features that are different from eukaryotes and prokaryotes: 1) Eukaryotes have a nucleus, prokaryotes do not. 2) DNA in eukaryotes is in the form of chromosomes, in prokaryotes the DNA is in a circle. 3) Eukaryotes can do endocytosis, fold their cell membrane around some external object and injest the object, prokaryotes can not. 4) Eukaryotes have a membrane lattice of proteins, actin and myacin, prokaryotes do not. 5) Eukaryotes have an endoplasmic reticulum and golgi body. 6) Eukaryotes reproduce asexually by dual binary division (both nucleus and cell divide by binary division), budding, or mitosis, prokaryotes reproduce by budding or binary division. If the nucleus is an engulfed prokaryote, this cell inherits the processes of nuclear DNA duplication and nucleus division (karyokinesis) from prokaryote binary division. Initially, both the nucleus and cell divide by binary division. FOOTNOTES 1. ^ Nature 396, 109 - 110 (12 November 1998); doi:10.1038/24030 Rickettsia, typhus and the mitochondrial connection MICHAEL W. GRAY 2. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 3. ^ Nature 392, 15 - 16 (05 March 1998); doi:10.1038/32033 A paradigm gets shifty W. FORD DOOLITTLE 4. ^ (h2 symbiosis) The chimeric eukaryote: Origin of the nucleus from the karyomastigont in amitochondriate protists Lynn Margulis*, Michael F. Dolan* , and Ricardo Guerrero file:/root/web/euk_nucleo6954. 5. ^ "Planctomycetes a phylum of emerging interest for microbial evolution and ecology John A. Fuerst" planctomycetes_a1.pdf and fuerst1.pdf 6. ^ Nature 392, 37 - 41 (05 March 1998); doi:10.1038/32096 The hydrogen hypothesis for the first eukaryote WILLIAM MARTIN* AND MIKLÓS MÜLLER 7. ^ Nature 431, 152 - 155 (09 September 2004); doi:10.1038/nature02848 The ring of life provides evidence for a genome fusion origin of eukaryotes MARIA C. RIVERA1,3,4 AND JAMES A. LAKE1,2,4 8. ^ Science, Vol 305, Issue 5685, 766-768 , 6 August 2004 EVOLUTIONARY BIOLOGY: The Birth of the Nucleus Elizabeth Pennisi 9. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005).0) origin of nuclear membrane/envelope, is anaerobic eukorig1 thru eukorig7 10. ^ S Blair Hedges, Hsiong Chen, Sudhir Kumar, Daniel YC Wang, Amanda S Thompson and Hidemi Wa, "A genomic timescale for the origin of eukaryotes", BMC Evolutionary Biology 2001, 1:4 doi:10.1186/1471-2148-1-4, (2001). 11. ^ S Blair Hedges, Hsiong Chen, Sudhir Kumar, Daniel YC Wang, Amanda S Thompson and Hidemi Wa, "A genomic timescale for the origin of eukaryotes", BMC Evolutionary Biology 2001, 1:4 doi:10.1186/1471-2148-1-4, (2001). |
[1] http://www.regx.de/m_organisms.php#planc to source: http://www.regx.de/m_organisms.p hp#plancto
[2] http://www.mansfield.ohio-state.edu/~sab edon/biol1080.htm source: http://www.mansfield.ohio-state. edu/~sabedon/biol1080.htm | |
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2,725,000,000 YBN 5 | 65) DNA in the nucleus changes from a single circular chromosome to linear chromosomes.1 2 3 4 Possibly the prokaryote ancestor of the first eukaryote had linear chromosomes since some prokaryotes (although very few) are known to have linear chromosomes instead of or in addition to a single circular chromosome. FOOTNOTES 1. ^ not all prokaryotes has circle of DNA: http://arjournals.annualreviews.or g/doi/full/10.1146/annurev.ecolsys.28.1. 391;jsessionid=npo4ogeI2anbnHbeKO 2. ^ Jumas-Bilak E, Maugard C, Michaux-Charachon S, Allardet-Servent A, Perrin A, et al. 1995. Study of the organization of the genomes of Escherichia coli, Brucella melitensis and Agrobacterium tumefaciens by insertion of a unique restriction site. Microbiology 141:2425-32 (Medline) 3. ^ Lezhava A, Kameoka D, Sugino H, Goshi K, Shinkawa H, et al. 1997. Chromosomal deletions in Streptomyces griseus that remove the afsA locus. Mol. Gen. Genet. 253:478-83 4. ^ Marconi RT, Casjens S, Munderloh UG, Samuels DS. 1996. Analysis of linear plasmid dimers in Borrelia burgdorferi sensu lato isolates: implications concerning the potential mechanisms of linear plasmid replication. J. Bact. 178:3357-61 5. ^ Ted Huntington, my guess due to absence of published info | ||
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2,720,000,000 YBN | 208) A eukaryote flagellum (cilium, undulipodium) evolves on early single cell eukaryotes. | ||
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2,720,000,000 YBN | 291) For the first time, a cell is not constantly synthesizing DNA and then having a division period (as is the case for all known prokaryotes), but this cell has a period in between cell division and DNA synthesis where DNA synthesis is not performed. Later some cells develop a stage after synthesis and before cell division.1 FOOTNOTES 1. ^ Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989).: p45 | ||
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2,719,000,000 YBN 3 | 302) If the first eukaryote nucleus was a prokaryote, synchronized duplication and division of organelle-nucleus and cytoplasm of early eukaryote cell evolves. Before this, eukaryote cell division usually results in one cell with no organelle-nuclei and a second cell with 2 organelle-nuclei. Perhaps the organelle-nuclei attach to the outer cell membrane in the same way the cytoplasmic DNA do, which allows new cytoplasm growth to separate the two organelle-nucleus in addition to the cytoplasmic DNA.1 2 FOOTNOTES 1. ^ Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989). 2. ^ based loosely on S Blair Hedges, Hsiong Chen, Sudhir Kumar, Daniel YC Wang, Amanda S Thompson and Hidemi Wa, "A genomic timescale for the origin of eukaryotes", BMC Evolutionary Biology 2001, 1:4 doi:10.1186/1471-2148-1-4, (2001). 3. ^ based loosely on S Blair Hedges, Hsiong Chen, Sudhir Kumar, Daniel YC Wang, Amanda S Thompson and Hidemi Wa, "A genomic timescale for the origin of eukaryotes", BMC Evolutionary Biology 2001, 1:4 doi:10.1186/1471-2148-1-4, (2001). |
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2,715,000,000 YBN | 72) Mitosis, asexual copying of a haploid (single set of chomosomes) eukaryote nucleus, evolves in eukaryotes. Before mitosis, there is a synthesis stage where DNA in the form of chromosomes are duplicated in the nucleus before the nucleus and cell divide.1 2 FOOTNOTES 1. ^ Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989).: types of mitosis, evolution of mitosis. 2. ^ BruscaCh05.pdf pleuromitosis, orthomitosis |
[1] Mitosis divides genetic information during cell division Source: http://www.ncbi.nlm.nih.gov/About/primer /genetics_cell.html This image is from the Science Primer, a work of the National Center for Biotechnology Information, part of the National Institutes of Health. As a work of the U.S. federal government, the image is in the public domain. source: http://en.wikipedia.org/wiki/Mit osis
[2] Prophase: The two round objects above the nucleus are the centrosomes. Note the condensed chromatin. from Gray's Anatomy. Unless stated otherwise, it is from the online edition of the 20th U.S. edition of Gray's Anatomy of the Human Body, originally published in 1918. Online editions can be found on Bartleby and also on Yahoo! source: | |
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2,710,000,000 YBN 5 6 | 73) Sex (cell and genetic fusion, syngamy, gametogamy) evolves in protists. Haploid (1 set of chromosomes) eukaryote cells merge and then their nuclei merge (karyogamy) to form the first diploid (2 sets of chromosomes) cells (the first zygote).1 2 This fusion of 2 haploid cells results in the first diploid single-celled organism, which then immediately divides (both nucleus and cytoplasm by single-division meiosis) back to two haploid cells. Possibly first, only cytoplasmic merging happened with nuclear merging (karyogamy) and nuclear division (karyokinesis) evolving later. Now, two cells with different DNA can mix providing more chance of variety/mutation. Two chromosome sets provides a backup copy of important genes (sequences that code for proteins, or nucleic acids) that might be lost with only a set of single chromosomes. The life cycle of future organisms will now have two phases, a gamophase (from n to 2n (until syngamy3 )), and zygophase (from 2n to n (until meiosis4 )). Gamoid cells are not haploid in polyploid organisms. FOOTNOTES 1. ^ Sir Gavin De Beer, "Atlas of Evolution", (London: Nelson, 1964). 2. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 3. ^ Ted Huntington. 4. ^ Ted Huntington. 5. ^ J. William Schopf, "Major Events in the History of Life", (Boston, MA: Jones and Bartlett Publishers, 1992).p57 (was) 6. ^ estimate based on diplomonads having sex repro, and origin of euk being (is now) |
[1] Zygotic Meiosis. GNU source: http://en.wikipedia.org/wiki/Ima ge:Zygotic_meiosis.png
[2] Gametic Meiosis. GNU source: http://en.wikipedia.org/wiki/Ima ge:Gametic_meiosis.png | |
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2,710,000,000 YBN | 206) Meiosis (one-step meiosis, one DNA duplication and a cell division of a diploid cell into 2 haploid cells) evolves.1 2 FOOTNOTES 1. ^ http://www.zoology.ubc.ca/~redfield/rese arch/clevelan.html 2. ^ Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989)., no cross over in one-division |
[1] GametoGenesis. COPYRIGHTED EDU source: http://www.bio.miami.edu/dana/10 4/gametogenesis.jpg [2] Sexual cycle oxymonas, identical to saccinobaculus, one step meiosis. haploid. COPYRIGHTED CANADA source: http://www.zoology.ubc.ca/~redfi eld/clevelan/oxymonas.GIF | |
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2,706,000,000 YBN | 299) Duplication of diploid DNA (after 2 haploid cells fuse) evolves. | ||
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2,705,000,000 YBN | 210) Mitosis of diploid cells evolves. This begins the "diplontic" life cycle (with gametic meiosis), where diploid cells (a zygote) can copy asexually through mitosis after merging. This organism, when haploid, cannot do mitosis (presumably haploid gamete mitosis will evolve much later in brown algae), and this is still true in all descendents (including humans) of this single celled organism. | ||
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2,704,000,000 YBN | 296) The origin of gender evolves: sex (cell and nucleus fusion) between two isogamous (same size) gametes but which have 2 different (+ and -) forms (genders).1 FOOTNOTES 1. ^ Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989). | ||
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2,703,000,000 YBN | 297) Sex (cell and nucleus fusion) between two different size gamete cells (heterogamy or anisogamy) evolves in protists.1 FOOTNOTES 1. ^ Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989). | ||
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2,700,000,000 YBN | 62) Oldest steranes (formed from sterols, molecules made by mitochondria in eukaryotes) found in northwestern Australia.1 2 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 2. ^ Science, Vol 285, Issue 5430, 1033-1036 , 13 August 1999 Archean Molecular Fossils and the Early Rise of Eukaryotes Jochen J. Brocks, 1,2* Graham A. Logan, 2 Roger Buick, 1 Roger E. Summons 2 | ||
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2,692,000,000 YBN | 300) Diploid cell fusion (Gamontogamy) evolves.1 2 3 4 FOOTNOTES 1. ^ Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989). p76,p79 2. ^ http://www.zoology.ubc.ca/~redfield/clev elan.html 3. ^ arjournals.annualreviews.org/doi/pdf/10. 1146/annurev.mi.17.100163.002105 diatoms do gamontogamy gamontogomy_diatoms_annurev.mi.17.100163 .002105.pdf 4. ^ http://arjournals.annualreviews.org/doi/ abs/10.1146%2Fannurev.ecolsys.28.1.391 annurev.ecolsys.28.1.391 (saved html file) | [1] The Oxymonad, Notila (diploid Pacific form) life cycle. COPYRIGHTED source: http://www.zoology.ubc.ca/~redfi eld/clevelan/notila.GIF | |
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2,690,000,000 YBN | 295) Meiosis (two step meiosis, two cell divisions with no stage in between which result in one diplid cell dividing into four haploid cells) evolves.1 FOOTNOTES 1. ^ http://www.zoology.ubc.ca/~redfield/rese arch/clevelan.html |
[1] GametoGenesis. COPYRIGHTED EDU source: http://www.bio.miami.edu/dana/10 4/gametogenesis.jpg [2] Sexual cycle oxymonas, identical to saccinobaculus, one step meiosis. haploid. COPYRIGHTED CANADA source: http://www.zoology.ubc.ca/~redfi eld/clevelan/oxymonas.GIF | |
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2,650,000,000 YBN 2 | 170) First bacteria live on land.1 FOOT NOTES 1. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 2. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). (2600-2700my) | ||
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2,558,000,000 YBN 2 | 171) Phylum Deinococcus-Thermus (Thermus Aquaticus {used in PCR}, Deinococcus radiodurans {can survive long exposure to radiation}) evolve now.1 FOOTNOTES 1. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 2. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). MORE INFO [1] Tree of Life. http://tolweb.org/tree/ [2] Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). |
[1] D. radiodurans growing on a nutrient agar plate. The red color is due to carotenoid pigment. Links to 816x711-pixel, 351KB JPG. Credit: M. Daly, Uniformed Services University of the Health Sciences NASA source: http://science.nasa.gov/newhome/ headlines/images/conan/D_rad_dish.jpg
[2] Photomicrograph of Deinococcus radiodurans, from www.ornl.gov/ORNLReview/ v34 The Oak Ridge National Laboratory United States Federal Government This work is in the public domain because it is a work of the United States Federal Government. This applies worldwide. See Copyright. source: http://en.wikipedia.org/wiki/Ima ge:Deinococcus.jpg | |
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2,558,000,000 YBN 3 4 | 172) Genetic comparison shows Eubacteria phylum, Cyanobacteria (ancestor of all eukaryote chloroplasts {plastids}) evolving now. There is a conflict between the interpretation of the geological and the genetic evidence as to if oxygen photosynthesis and cyanobacteria evolved earlier around 3800mybn or here at 2500mybn.1 2 FOOTNO TES 1. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 2. ^ S. Blair Hedges and Sudhir Kumar, "Genomic clocks and evolutionary timescales", Trends in Genetics Volume 19, Issue 4 , April 2003, Pages 200-206, (2003). 3. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 4. ^ S. Blair Hedges and Sudhir Kumar, "Genomic clocks and evolutionary timescales", Trends in Genetics Volume 19, Issue 4 , April 2003, Pages 200-206, (2003). MORE INFO [1] Tree of Life. http://tolweb.org/tree/ [2] Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). [3] Journal of Molecular Evolution Publisher: Springer-Verlag New York ISSN: 0022-2844 (Paper) 1432-1432 (Online) Issue: Volume 42, Number 2 Date: February 1996 Pages: 194 - 200 [4] Phylogenetic Relationships of Nonaxenic Filamentous Cyanobacterial Strains Based on 16S rRNA Sequence Analysis jme_42_2_1996.pdf [5] http://en.wikipedia.org/wiki/Cyanobacter ia |
[1] Oscillatoria COPYRIGHTED EDU source: http://www.stcsc.edu/ecology/alg ae/oscillatoria.jpg
[2] Lyngbya COPYRIGHTED EDU source: http://www.stanford.edu/~bohanna n/Media/LYNGB5.jpg | |
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2,558,000,000 YBN 2 | 315) Phylum Chloroflexi, (Green Non-Sulphur) evolve now.1 FOOTNOTES 1. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). 2. ^ Battistuzzi, Feijao, Hedges, "A Genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land", BMC Evolutionary Biology, (2004). MORE INFO [1] Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). [2] Tree of Life http://tolweb.org/tree/ |
[1] Chloroflexus photomicrograph from Doe Joint Genome Institute of US Dept Energy PD source: http://en.wikipedia.org/wiki/Ima ge:Chlorofl.jpg | |
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2,500,000,000 YBN | 52) End Archean Era, Start Proterozoic Era.1 2 FOOTNOTES 1. ^ The geological Society of America ucmp.berkeley.edu 2. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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2,500,000,000 YBN | 56) Banded Iron Formations start to appear in many places.1 2 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 2. ^ greenspirit.uk | ||
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2,400,000,000 YBN | 59) Very large ice age that lasts 200 million years starts now.1 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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2,335,000,000 YBN 2 | 290) The nucleolus, a sphere in the nucleus that makes ribosomes, evolves.1 FOOTNOTES 1. ^ Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989).: p48 nucleolus divides 2. ^ Ted Huntington guess |
[1] Nucleolus, COPYRIGHTED source: http://www.eccentrix.com/members /chempics/Slike/cell/Nucleolus.jpg
[2] With the combination of x-rays from the Advanced Light Source and a new protein-labeling technique, scientists can see the distribution of the nucleoli within the nucleus of a mammary epithelial cell. USG PD source: http://www.lbl.gov/Science-Artic les/Archive/xray-inside-cells.html | |
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2,330,000,000 YBN | 198) Rough and smooth endoplasmic reticulum evolves in eukaryote cell. |
[1] Figure 1 : Image of nucleus, endoplasmic reticulum and Golgi apparatus. (1) Nucleus. (2) Nuclear pore. (3) Rough endoplasmic reticulum (RER). (4) Smooth endoplasmic reticulum (SER). (5) Ribosome on the rough ER. (6) Proteins that are transported. (7) Transport vesicle. (8) Golgi apparatus. (9) Cis face of the Golgi apparatus. (10) Trans face of the Golgi apparatus. (11) Cisternae of the Golgi apparatus. I am the copyright holder of that image (I might even have the CorelDraw file around somewhere:-), and I hereby place the image and all partial images created from it in the public domain. So, you are free to use it any way you like. In fact, I am delighted that one of my drawings makes it into print! I can mail you the .cdr file, if you like (and if I can find it), if you need a better resolution for printing. Yours, Magnus Manske Source: [1]. See also User:Magnus Manske source: http://en.wikipedia.org/wiki/Ima ge:Nucleus_ER_golgi.jpg | |
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2,325,000,000 YBN | 199) Golgi Body (Golgi Apparatus, dictyosome) evolves in eukaryote cell. |
[1] Figure 1: Image of nucleus, endoplasmic reticulum and Golgi apparatus: (1) Nucleus, (2) Nuclear pore, (3) Rough endoplasmic reticulum (RER), (4) Smooth endoplasmic reticulum (SER), (5) Ribosome on the rough ER, (6) Proteins that are transported, (7) Transport vesicle, (8) Golgi apparatus, (9) Cis face of the Golgi apparatus, (10) Trans face of the Golgi apparatus, (11) Cisternae of the Golgi apparatus, (12) Secretory vesicle, (13) Plasma membrane, (14) Exocytosis, (15) Cytoplasm, (16) Extracellular space. source: http://en.wikipedia.org/wiki/Ima ge:Nucleus_ER_golgi_ex.jpg | |
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2,310,000,000 YBN | 200) The golgi body in eukaryote cells makes lysosomes which fuse with endosomes. The various molecules in lysosomes digest the contents of the endosome, which then exits the cell as waste. |
[1] Figure 1: Image of nucleus, endoplasmic reticulum and Golgi apparatus: (1) Nucleus, (2) Nuclear pore, (3) Rough endoplasmic reticulum (RER), (4) Smooth endoplasmic reticulum (SER), (5) Ribosome on the rough ER, (6) Proteins that are transported, (7) Transport vesicle, (8) Golgi apparatus, (9) Cis face of the Golgi apparatus, (10) Trans face of the Golgi apparatus, (11) Cisternae of the Golgi apparatus, (12) Secretory vesicle, (13) Plasma membrane, (14) Exocytosis, (15) Cytoplasm, (16) Extracellular space. source: http://sun.menloschool.org/~cwea ver/cells/e/lysosomes/
source: http://en.wikipedia.org/wiki/Ima ge:Nucleus_ER_golgi_ex.jpg | |
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2,305,000,000 YBN | 63) A parasitic bacterium, a bacterium that can only live in other bacteria, closely related to Rickettsia prowazekii, an aerobic alpha-proteobacteria that causes louse-borne typhus, enters an early eukaryote cell. As time continues a symbiotic relationship evolves, where the Rickettsia forms the mitochondria, organelles of every euokaryote cell. The mitochondria perform the Acid Citric Cycle (Krebs Cycle), using oxygen to breakdown glucose into CO2 and H2O, and provide up 38 ATP molecules. Mitochondria reproduce by themselves, and are not created by the DNA in the cell nucleus. As time continues some of the DNA from the mitochondria merges with the cell nucleus DNA. Mitochondria produce sterol used to make the eukaryote cell wall flexible. Because mitochondria need Oxygen, but the level of oxygen is very low on earth, oxygen may be provided by photosynthesizing cyanobacteria living near these cells. All eukaryotes alive today either have mitochondria except the amitochondriate excavates (metamonads), the most ancient of the eukaryotes alive today. That parabasalids have hydrogenosomes, anaerobic organelles that seem to have evolved from mitochondria, many people think amitochondriate species lost their mitochondria over time.1 FOOTNOTES 1. ^ http://comenius.susqu.edu/BI/202/Protist s/EUKARYA-DOMAIN.htm |
[1] Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. source: http://nar.oxfordjournals.org/co ntent/vol26/issue4/images/gkb18201.gif
[2] Figure 1 Phylogenetic tree of eukaryotes based on ultrastructural and molecular data. Organisms are sub-divided into main groups as discussed in the text. Only a few representative species for which complete (or almost complete) mtDNA sequences are known are shown in each lineage. In some cases, line drawings or actual pictures of the organisms are provided (Acanthamoeba, M. Nagata; URL: http://protist.i.hosei.ac.jp/PDB/PCD3379 /htmls/21.html; Allomyces, Tom Volk; URL: http://botit.botany.wisc.edu/images/332/ Chytridiomycota/Allomyces_r_So_pa/A._arb uscula_pit._sporangia_tjv.html; Amoebidium, URL: http://cgdc3.igmors.upsud.fr/microbiolog ie/mesomycetozoaires.htm; Marchantia, URL: http://www.science.siu.edu/landplants/He patophyta/images/March.female.JPEG Scenedesmus, Entwisle et al., http://www.rbgsyd.gov.au/_data/page/1824 /Scenedesmus.gif). The color-coding of the main groups (alternating between dark and light blue) on the outer circle corresponds to the color-coding of the species names. Unbroken lines indicate phylogenetic relationships that are firmly supported by available molecular data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional sequence data. [t: why not color code or add which type of mito?] source: http://arjournals.annualreviews. org/doi/full/10.1146/annurev.genet.37.11 0801.142526 | |
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2,303,000,000 YBN 4 | 203) Bikonts (two cilia) evolve from Unikonts (one cilium). Bikonts (also called anterokonts for having anterior {forward facing} cilia) will evolve into the vast majority of the Protist and all of the Plant Kingdoms. The Unikonts will evolve into the ameobozoa (tenatively), and the opisthokonts (ancestrally posterior cilium) which include the entire Fungi and Animal Kingdoms.1 2 3 FOOTNOTES 1. ^ Nucleic Acids Research Pages 865-878 v26 4 865 MW Gray, BF Lang, R Cedergren, GB Golding, C Lemieux, D Sankoff, M Turmel, N Brossard, E Delage, TG Littlejohn, I Plante, P Rioux, D Saint-Louis, Y Zhu, and G Burger 2. ^ Genome structure and gene content in protist mitochondrial DNAs J Mol Evol (2003) 56:540 563, 2003 56:540-563 Cavalier-Smith Journal of Molecular Evolution Phylogeny of Choanozoa, Apusozoa, and Other Protozoa and Early Eukaryote Megaevolution Thomas Cavalier-Smith, Ema E.-Y. Chao 3. ^ Cav-Smith science vol297 issue 5578 07-05-2002 4. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). MORE INFO [1] THOMAS CAVALIER-SMITH, "Economy, Speed and Size Matter: Evolutionary Forces Driving Nuclear Genome Miniaturization and Expansion", * Oxford Journals * Life Sciences * Annals of Botany * Volume 95, Number 1 *, (2005). [2] Thomas Cavalier-Smith and Ema E. -Y. Chao, "Phylogeny of Choanozoa, Apusozoa, and Other Protozoa and Early Eukaryote Megaevolution", Springer New York, (2003). [3] Michael W. Gray, B. Franz Lang, Robert Cedergren, G. Brian Golding, Claude Lemieux, David San, "Genome structure and gene content in protist mitochondrial DNAs", Oxford Journals, (1997). |
[1] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. source: | |
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2,300,000,000 YBN | 47) Most recent evidence of uraninite, a mineral that cannot exist for much time if exposed to oxygen, indicating that free oxygen is accumulating in the air of earth for the first time.1 FOOTN OTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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2,300,000,000 YBN | 48) Oldest Red Beds, iron oxide formed on land, begin here and are evidence of more free oxygen in the air of earth.1 2 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 2. ^ http://www.es.ucsc.edu/~pkoch/lectures/l ecture5.html |
[1] http://www.kgs.ukans.edu/Extension/redhi lls/redhills.html source: | |
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2,300,000,000 YBN 4 5 6 | 219) Genetic comparison shows the oldest line of eukaryotes still in existence, the oldest living protists, in the Phylum "Metamonada" (Excavates) originating now. 1 2 3 This is where the eukaryote line is created and separates from the archaebacteria (archaea) line. Most of these species have an excavated ventral feeding groove, and all lack mitochondria. Mitochondria are thought to have been lost secondarily, although this is not certain. FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 6. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). |
[1] Giardia lamblia, a parasitic flagellate that causes giardiasis. Image from public domain source at http://www.nigms.nih.gov/news/releases/i mages/para.jpg source: http://www.nigms.nih.gov/news/re leases/images/para.jpg
[2] . The cysts are hardy and can survive several months in cold water. Infection occurs by the ingestion of cysts in contaminated water, food, or by the fecal-oral route (hands or fomites) . In the small intestine, excystation releases trophozoites (each cyst produces two trophozoites) . Trophozoites multiply by longitudinal binary fission, remaining in the lumen of the proximal small bowel where they can be free or attached to the mucosa by a ventral sucking disk . Encystation occurs as the parasites transit toward the colon. The cyst is the stage found most commonly in nondiarrheal feces . Because the cysts are infectious when passed in the stool or shortly afterward, person-to-person transmission is possible. While animals are infected with Giardia, their importance as a reservoir is unclear. source: http://www.dpd.cdc.gov/dpdx/HTML /Giardiasis.asp?body=Frames/G-L/Giardias is/body_Giardiasis_page1.htm | |
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2,000,000,000 YBN 7 8 9 10 | 293) Genetic comparison shows the the Eukaryote Phylum "Loukozoa" (Jakobea and Malawimonadea) originating now. These species have mitochondria with tubular cristae, and are the most ancient species that still have mitochondria.1 2 3 4 This species is the most ancient known species to have a shell. This first hard shells (lorika) made of calcium carbonate (Calcite CaCO3), plates of silica (SiO2), or carbon-based molecules evolve around the single-celled species living in the ocean. 5 Perhaps this shell served to protect the cell from external damage from being eaten by other eukaryotes (zooplankton), infection by bacteria or viruses, control of buoyancy, to filter UV light, against damage by non-living sources. 6 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 4. ^ S. L. Baldauf, "The Deep Roots of Eukaryotes", Science 13 June 2003: Vol. 300. no. 5626, pp. 1703 - 1706 DOI: 10.1126/science.1085544, (2003). 5. ^ http://www.iscid.org/encyclopedia/Lorica 6. ^ "Coccolith". Wikipedia. Wikipedia, 2008. http://en.wikipedia.org/wiki/Coccolith 7. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 8. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 9. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 10. ^ estimate from S. L. Baldauf, "The Deep Roots of Eukaryotes", Science 13 June 2003: Vol. 300. no. 5626, pp. 1703 - 1706 DOI: 10.1126/science.1085544, (2003). |
[1] Histiona. This drawing was made by D. J. Patterson. COPYRIGHTED EDU source: http://microscope.mbl.edu/script s/microscope.php?func=imgDetail&imageID= 3479
[2] Histiona (hist-ee-own-a) is a jakobid flagellate related to Jakoba. As with other excavates, there is a ventral groove and the flagella insert at the head of the groove. There are two flagella, one lying in the groove and one curving outwards from the point of insertion. The margins of the groove can be mistaken for flagella. Unlike most other excavates, Histiona sits in a stalked lorica when feeding. Lorica with a cyst is evident. Phase contrast. This picture was taken by David Patterson, Linda Amaral Zettler, Mike Peglar and Tom Nerad from cultures and other materials maintained at the American Type Culture Collection during 2001. COPYRIGHTED EDU source: http://microscope.mbl.edu/script s/microscope.php?func=imgDetail&imageID= 435 | |
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1,990,000,000 YBN | 202) Eukaryotes with discoidal cristae mitochondria split from the tubular christae line.1 This is the origin of the Discicristata: species that have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove.2 FOOTNOTES 1. ^ Nucleic Acids Research Pages 865-878 v26 4 865 MW Gray, BF Lang, R Cedergren, GB Golding, C Lemieux, D Sankoff, M Turmel, N Brossard, E Delage, TG Littlejohn, I Plante, P Rioux, D Saint-Louis, Y Zhu, and G Burger 2. ^ Genome structure and gene content in protist mitochondrial DNAs http://www.sciencemag.org/cgi/content/fu ll/300/5626/1703/FIG1 |
[1] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. source: http://nar.oxfordjournals.org/co ntent/vol26/issue4/images/gkb18201.gif | |
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1,990,000,000 YBN | 301) Haplodiplontic (Diplohaplontic, Diplobiontic) life cycle (organism with both diploid and haploid "alternate life stages" that reproduce asexually by mitosis) with "sporic meiosis" evolves. In this life cycle haploid gametes fuse to form a diploid zygote which divides by meiosis producing haploid spores that produce (differentiate?) gametes, starting the cycle again. Initially these species are single celled in both stages (like Haptophyta). |
[1] Figure 23.1.Plants have haplodiplontic life cycles that involve mitotic divisions (resulting in multicellularity) in both the haploid and diploid generations (paths A and D). Most animals are diplontic and undergo mitosis only in the diploid generation (paths B and D). Multicellular organisms with haplontic life cycles follow paths A and C. COPYRIGHTED EDU source: http://zygote.swarthmore.edu/pla ntfig1.gif
[2] Drawn by self for Biological life cycle Based on Freeman & Worth's Biology of Plants (p. 171). GNU source: http://en.wikipedia.org/wiki/Ima ge:Sporic_meiosis.png | |
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1,988,000,000 YBN 3 | 317) Eukaryotes that have mitochondria with flat christae evolve from those with tubular christae.1 2 FOOTNOTES 1. ^ http://nar.oxfordjournals.org/cgi/conten t/full/26/4/865 2. ^ http://microscope.mbl.edu/scripts/protis t.php?func=integrate&myID=P1901&chinese_ flag=&system=&version=&documentID=&exclu deNonLinkedIn=&imagesOnly= 3. ^ guess based on one jakobid having tubular that change to flat, aside from that cryptomonads are firs |
[1] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. source: http://nar.oxfordjournals.org/co ntent/vol26/issue4/images/gkb18201.gif | |
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1,982,000,000 YBN 4 5 6 | 87) Genetic comparison shows the most primitive living members of the Phylum "Euglenozoa" (euglenids, leishmania, trypanosomes, kinetoplastids) evolved at this time.1 2 3 This is the oldest eukaryote to exhibit colonialism. Perhaps eukaryote colonialism is partially or fully inherited from prokaryotes, but colonialism may have evolved independently again in eukaryotes. This is the most ancient species known to have a cell covering, which is of the type "pellicle". FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Russell F. Doolittle, Da-Fei Feng, Simon Tsang, Glen Cho, Elizabeth Little, "Determining Divergence Times of the Major Kingdoms of Living Organisms with a Protein Clock", Science, (1996). 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1961) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1600mybn) 6. ^ Russell F. Doolittle, Da-Fei Feng, Simon Tsang, Glen Cho, Elizabeth Little, "Determining Divergence Times of the Major Kingdoms of Living Organisms with a Protein Clock", Science, (1996). (1800-1900 for eukaryote/prokaryote separation) |
[1] euglena source: http://www.fcps.k12.va.us/Stratf ordLandingES/Ecology/mpages/euglena.htm
[2] euglena source: http://protist.i.hosei.ac.jp/PDB /Images/Mastigophora/Euglena/genus1L.jpg | |
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1,982,000,000 YBN 5 6 7 | 294) Genetic comparison shows the Phylum "Percolozoa" (also called "Heterolobosea"1 ) (acrasid slime molds) evolved at this time.2 3 4 FOOTN OTES 1. ^ Ted Huntington. 2. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 1961mybn 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 1600 mybn 4. ^ Russell F. Doolittle, Da-Fei Feng, Simon Tsang, Glen Cho, Elizabeth Little, "Determining Divergence Times of the Major Kingdoms of Living Organisms with a Protein Clock", Science, (1996). 1800-1900 mybn 5. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 1961mybn (1961) 6. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 1600 mybn (1600mybn) 7. ^ Russell F. Doolittle, Da-Fei Feng, Simon Tsang, Glen Cho, Elizabeth Little, "Determining Divergence Times of the Major Kingdoms of Living Organisms with a Protein Clock", Science, (1996). 1800-1900 mybn (1800-1900(for eukaryote/prokaryote separation) |
[1] Stages of Naegleria fowleri, a member of the Percolozoa. Adapted from Image:Free-living amebic infections.gif, which is from the CDC. PD source: http://en.wikipedia.org/wiki/Ima ge:Naegleria.png
[2] CLASS Heterolobosea ORDER Schizopyrenida Heteramoeba: The flagellated form is large (30 �m), two flagella, an elongate cytostome curving around the anterior of the cell and forming a groove. Nucleus with peripheral chromatin. Probably feeds and divides as a flagellate. One species. This genus is most like Paratetramitus from which it can be distinguished by peripheral location of chromatin material. Cysts without pores, excystment through a weak region of wall. Marine. Heteramoeba (het-err-a-me-ba) a naked heterolobose amoeba, distinguished from other types of naked amoebae with lobose pseudopodia largely by ultrastructural features, but trophic heterolobose amoebae tend to form their pseudopodially suddenly rather than progressively. Phase contrast. This picture was taken by David Patterson, Linda Amaral Zettler, Mike Peglar and Tom Nerad from cultures and other materials maintained at the American Type Culture Collection during 2001. NONCOMMERCIAL USE source: http://microscope.mbl.edu/script s/microscope.php?func=imgDetail&imageID= 413 | |
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1,980,000,000 YBN 1 | 38) Multicellularity evolves in a protist. Multicellularity is a very important event in the evolution of life on earth. With multicellular organisms, larger sized organisms could evolve. There are many uncertainties surrounding the origin of multicellularity. Multicellularity may have evolved independently for Plants, Fungi and Animals, or multicellularity may have evolved only once in eukaryotes. The key feature of this cell is that a multicellular organism is made from a single cell and the multicellular organism is not a collection of independent cells (colonialism). The main difference between this organism and single-celled organisms is the way the cells stay fastened together after cell division. Which species was the first multicellular species is not clear. Multicellularity is found in all 3 life cycles (haplontic, diplontic, haplodiplontic). The 3 main life cycle types (haplontic, etc.) probably evolved in single cell species before multicellularity evolved. If multicellularity evolved once and is inherited, perhaps all multicellular organism descended from a single haplodiplontic organism. These multicellular organisms have undifferentiated cells in the multicellular stage (all cells in the haploid or diploid multicellular organism are made of one kind of cell). FOOTNO TES 1. ^ Michael Sleigh, "Protozoa and Other Protists", (London; New York: Edward Arnold, 1989). | ||
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1,978,000,000 YBN 1 | 15) Multicellularity with differentiation evolves. Multicellular organisms are no longer all haploid or diploid gamete producing cells (or spore producing if haplodiplontic), but are made of gamete (or spore) producing cells in addition to somatic cells which copy asexually through mitosis. Now, in addition to being large multicell organisms, multicellular organisms can have differentiated cells that form a variety of different shaped structures, and perform different functions. FOOTNOTES 1. ^ Ted Huntington. guess. is after haploid mitosis? after fusion? | ||
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1,973,000,001 YBN 4 5 6 | 88) Genetic comparison shows the ancestor of the "Chromalveolates" evolving now. Chromalveolates include the Chromista and Alveolata. The Chromista include the 3 Phyla Haptophyta, Cryptophyta (Cryptomonads), and Heterokontophyta (brown algae {kelp}, diatoms, water molds). Alveolata include the 3 Phyla Dinoflagellata, Apicomplexa (Malaria, Toxoplasmosis), and Ciliophora (ciliates).1 2 3 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1973mybn) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1600mybn) 6. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch MORE INFO [1] "Brown alga". Wikipedia. Wikipedia, 2008. http://en.wikipedia.org/wiki/Brown_alga |
[1] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703
[2] Beautiful marine diatoms as seen through a microscope. These tiny phytoplankton are encased within a silicate cell wall. Image ID: corp2365, NOAA Corps Collection Photographer: Dr. Neil Sullivan, University of Southern Calif. NOAA This image is a work of the National Oceanic and Atmospheric Administration, taken or made during the course of an xxxxx? official duties. As works of the U.S. federal government, all NOAA images are in the public domain. source: http://en.wikipedia.org/wiki/Ima ge:Diatoms_through_the_microscope.jpg | |
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1,972,000,000 YBN 4 5 6 | 304) Genetic comparison shows the ancestor of Chromalveolate Phlyum Haptophyta evolving now.1 2 3 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000).has heterkonts before ciliophora and apicomplexa branch 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1973mybn) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1600mybn) 6. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). (has heterkonts before ciliophora and apicomplexa branch) |
[1] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703
[2] Emiliania huxleyi, a coccolithophore. Photo courtesy Dr. Markus Geisen - photographer, and The Natural History Museum. PD source: http://en.wikipedia.org/wiki/Ima ge:Emiliania_huxleyi_3.jpg | |
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1,971,000,000 YBN 4 5 6 | 305) Genetic comparison shows the ancestor of the Chromalveolate Phylum "Cryptophyta" (Cryptomonads) evolving now.1 2 3 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1973mybn) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1600mybn) 6. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch |
[1] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group COPYRIGHTED source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703
[2] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. COPYRIGHTED source: http://nar.oxfordjournals.org/cg i/content/full/26/4/865 | |
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1,970,000,000 YBN 4 5 6 | 306) Genetic comparison shows the ancestor of the Chromalveolate Phylum "Heterokontophyta" (Heterokonts also called Stramenopiles) evolving now. Heterokonts include brown algae, diatoms, golden algae, axodines, yellow-green algae, water moulds and slime nets.1 2 3 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1973mybn) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1600mybn) 6. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch |
[1] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group COPYRIGHTED source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703
[2] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. COPYRIGHTED source: http://nar.oxfordjournals.org/cg i/content/full/26/4/865 | |
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1,969,000,000 YBN 4 5 6 | 307) Chromalveolate Heterokont, Brown Algae (Phaeophyta) evolves now.1 2 3 Brown Algae is the most genetically ancient multicellular organism still living on earth. In addition to being first to evolve multicellularity, cell differentiation (cells of different types) is already present in all brown algae. FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1973mybn) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1600mybn) 6. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch |
[1] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group COPYRIGHTED source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703
[2] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. COPYRIGHTED source: http://nar.oxfordjournals.org/cg i/content/full/26/4/865 | |
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1,968,000,000 YBN 4 5 6 | 308) Chromalveolate Heterokont, Diatoms evolve.1 2 3 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1973mybn) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1600mybn) 6. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch |
[1] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group COPYRIGHTED source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703
[2] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. COPYRIGHTED source: http://nar.oxfordjournals.org/cg i/content/full/26/4/865 | |
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1,967,000,000 YBN 4 5 6 | 309) Chromalveolate Heterokont, Water molds (Oomycetes OemISETEZ) evolve.1 2 3 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1973mybn) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1600mybn) 6. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch |
[1] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group COPYRIGHTED source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703
[2] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. COPYRIGHTED source: http://nar.oxfordjournals.org/cg i/content/full/26/4/865 | |
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1,966,000,000 YBN 4 5 6 | 310) Chromalveolate Alveolata (Ciliates, Dinoflagellates, Apicomplexans) evolve.1 2 3 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1973mybn) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1600mybn) 6. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch |
[1] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group COPYRIGHTED source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703
[2] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. COPYRIGHTED source: http://nar.oxfordjournals.org/cg i/content/full/26/4/865 | |
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1,964,000,000 YBN 4 5 6 | 312) Ciliates evolve.1 2 3 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1973mybn) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1600mybn) 6. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch |
[1] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group COPYRIGHTED source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703
[2] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. COPYRIGHTED source: http://nar.oxfordjournals.org/cg i/content/full/26/4/865 | |
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1,963,000,000 YBN 4 5 6 | 313) Dinoflagellates evolve.1 2 3 FOOTN OTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1973mybn) 5. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch (1600mybn) 6. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). |
[1] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group COPYRIGHTED source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703
[2] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. COPYRIGHTED source: http://nar.oxfordjournals.org/cg i/content/full/26/4/865 | |
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1,962,000,000 YBN 4 5 6 | 314) Apicomplexans evolve.1 2 3 FOOTNOT ES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1973mybn) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1600mybn) 6. ^ Sandra L. Baldauf, A. J. Roger, I. Wenk-Siefert, W. F. Doolittle, "A Kingdom-Level Phylogeny of Eukaryotes Based on Combined Protein Data", Science, Vol 290, num 5493, p 972, (2000). has heterkonts before ciliophora and apicomplexa branch MORE INFO [1] http://www.sirinet.net/~jgjohnso/apbio30 .html |
[1] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group COPYRIGHTED source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703
[2] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. COPYRIGHTED source: http://nar.oxfordjournals.org/cg i/content/full/26/4/865 | |
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1,961,000,000 YBN 3 4 | 89) Genetic comparison shows Rhizaria (the Phyla "Radiolaria", "Cercozoa", and "Foraminifera") evolve now.1 2 This marks the beginning of the protists described as "amoeboid", because they have pseudopods. FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). has 1600my for excavates, discricristales, rhizaria, chromalveolates, (1600my) 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). I use this estimate |
[1] FIG. 2. The tree of life based on molecular, ultrastructural and palaeontological evidence. Contrary to widespread assumptions, the root is among the eubacteria, probably within the double-enveloped Negibacteria, not between eubacteria and archaebacteria (Cavalier-Smith, 2002b); it may lie between Eobacteria and other Negibacteria (Cavalier-Smith, 2002b). The position of the eukaryotic root has been nearly as controversial, but is less hard to establish: it probably lies between unikonts and bikonts (Lang et al., 2002; Stechmann and Cavalier-Smith, 2002, 2003). For clarity the basal eukaryotic kingdom Protozoa is not labelled; it comprises four major groups (alveolates, cabozoa, Amoebozoa and Choanozoa) plus the small bikont phylum Apusozoa of unclear precise position; whether Heliozoa are protozoa as shown or chromists is uncertain (Cavalier-Smith, 2003b). Symbiogenetic cell enslavement occurred four or five times: in the origin of mitochondria and chloroplasts from different negibacteria, of chromalveolates by the enslaving of a red alga (Cavalier-Smith, 1999, 2003; Harper and Keeling, 2003) and in the origin of the green plastids of euglenoid (excavate) and chlorarachnean (cercozoan) algae-a green algal cell was enslaved either by the ancestral cabozoan (arrow) or (less likely) twice independently within excavates and Cercozoa (asterisks) (Cavalier-Smith, 2003a). The upper thumbnail sketch shows membrane topology in the chimaeric cryptophytes (class Cryptophyceae of the phylum Cryptista); in the ancestral chromist the former food vacuole membrane fused with the rough endoplasmic reticulum placing the enslaved cell within its lumen (red) to yield the complex membrane topology shown. The large host nucleus and the tiny nucleomorph are shown in blue, chloroplast green and mitochondrion purple. In chlorarachneans (class Chlorarachnea of phylum Cercozoa) the former food vacuole membrane remained topologically distinct from the ER to become an epiplastid membrane and so did not acquire ribosomes on its surface, but their membrane topology is otherwise similar to the cryptophytes. The other sketches portray the four major kinds of cell in the living world and their membrane topology. The upper ones show the contrasting ancestral microtubular cytoskeleton (ciliary roots, in red) of unikonts (a cone of single microtubules attaching the single centriole to the nucleus, blue) and bikonts (two bands of microtubules attached to the posterior centriole and an anterior fan of microtubules attached to the anterior centriole). The lower ones show the single plasma membrane of unibacteria (posibacteria plus archaebacteria), which were ancestral to eukaryotes and the double envelope of negibacteria, which were ancestral to mitochondria and chloroplasts (which retained the outer membrane, red). source: http://aob.oxfordjournals.org/cg i/content/full/95/1/147/FIG2
[2] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group. source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703 | |
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1,961,000,000 YBN 3 4 | 320) Rhizaria Phylum "Cercozoa" evolve now.1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). has 1600mybn for excavates, discricristales, rhizaria, chromalveolates 2. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). has 1600mybn for excavates, discricristales, rhizaria, chromalveolates (1600mybn) 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). |
[1] FIG. 2. The tree of life based on molecular, ultrastructural and palaeontological evidence. Contrary to widespread assumptions, the root is among the eubacteria, probably within the double-enveloped Negibacteria, not between eubacteria and archaebacteria (Cavalier-Smith, 2002b); it may lie between Eobacteria and other Negibacteria (Cavalier-Smith, 2002b). The position of the eukaryotic root has been nearly as controversial, but is less hard to establish: it probably lies between unikonts and bikonts (Lang et al., 2002; Stechmann and Cavalier-Smith, 2002, 2003). For clarity the basal eukaryotic kingdom Protozoa is not labelled; it comprises four major groups (alveolates, cabozoa, Amoebozoa and Choanozoa) plus the small bikont phylum Apusozoa of unclear precise position; whether Heliozoa are protozoa as shown or chromists is uncertain (Cavalier-Smith, 2003b). Symbiogenetic cell enslavement occurred four or five times: in the origin of mitochondria and chloroplasts from different negibacteria, of chromalveolates by the enslaving of a red alga (Cavalier-Smith, 1999, 2003; Harper and Keeling, 2003) and in the origin of the green plastids of euglenoid (excavate) and chlorarachnean (cercozoan) algae-a green algal cell was enslaved either by the ancestral cabozoan (arrow) or (less likely) twice independently within excavates and Cercozoa (asterisks) (Cavalier-Smith, 2003a). The upper thumbnail sketch shows membrane topology in the chimaeric cryptophytes (class Cryptophyceae of the phylum Cryptista); in the ancestral chromist the former food vacuole membrane fused with the rough endoplasmic reticulum placing the enslaved cell within its lumen (red) to yield the complex membrane topology shown. The large host nucleus and the tiny nucleomorph are shown in blue, chloroplast green and mitochondrion purple. In chlorarachneans (class Chlorarachnea of phylum Cercozoa) the former food vacuole membrane remained topologically distinct from the ER to become an epiplastid membrane and so did not acquire ribosomes on its surface, but their membrane topology is otherwise similar to the cryptophytes. The other sketches portray the four major kinds of cell in the living world and their membrane topology. The upper ones show the contrasting ancestral microtubular cytoskeleton (ciliary roots, in red) of unikonts (a cone of single microtubules attaching the single centriole to the nucleus, blue) and bikonts (two bands of microtubules attached to the posterior centriole and an anterior fan of microtubules attached to the anterior centriole). The lower ones show the single plasma membrane of unibacteria (posibacteria plus archaebacteria), which were ancestral to eukaryotes and the double envelope of negibacteria, which were ancestral to mitochondria and chloroplasts (which retained the outer membrane, red). source: http://aob.oxfordjournals.org/cg i/content/full/95/1/147/FIG2
[2] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group. source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703 | |
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1,960,000,000 YBN 3 4 | 319) Rhizaria Phylum "Radiolaria" evolve now.1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 1600mybn for excavates, discricristales, rhizaria, chromalveolates 2. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 1600mybn for excavates, discricristales, rhizaria, chromalveolates (1600my) 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). |
[1] FIG. 2. The tree of life based on molecular, ultrastructural and palaeontological evidence. Contrary to widespread assumptions, the root is among the eubacteria, probably within the double-enveloped Negibacteria, not between eubacteria and archaebacteria (Cavalier-Smith, 2002b); it may lie between Eobacteria and other Negibacteria (Cavalier-Smith, 2002b). The position of the eukaryotic root has been nearly as controversial, but is less hard to establish: it probably lies between unikonts and bikonts (Lang et al., 2002; Stechmann and Cavalier-Smith, 2002, 2003). For clarity the basal eukaryotic kingdom Protozoa is not labelled; it comprises four major groups (alveolates, cabozoa, Amoebozoa and Choanozoa) plus the small bikont phylum Apusozoa of unclear precise position; whether Heliozoa are protozoa as shown or chromists is uncertain (Cavalier-Smith, 2003b). Symbiogenetic cell enslavement occurred four or five times: in the origin of mitochondria and chloroplasts from different negibacteria, of chromalveolates by the enslaving of a red alga (Cavalier-Smith, 1999, 2003; Harper and Keeling, 2003) and in the origin of the green plastids of euglenoid (excavate) and chlorarachnean (cercozoan) algae-a green algal cell was enslaved either by the ancestral cabozoan (arrow) or (less likely) twice independently within excavates and Cercozoa (asterisks) (Cavalier-Smith, 2003a). The upper thumbnail sketch shows membrane topology in the chimaeric cryptophytes (class Cryptophyceae of the phylum Cryptista); in the ancestral chromist the former food vacuole membrane fused with the rough endoplasmic reticulum placing the enslaved cell within its lumen (red) to yield the complex membrane topology shown. The large host nucleus and the tiny nucleomorph are shown in blue, chloroplast green and mitochondrion purple. In chlorarachneans (class Chlorarachnea of phylum Cercozoa) the former food vacuole membrane remained topologically distinct from the ER to become an epiplastid membrane and so did not acquire ribosomes on its surface, but their membrane topology is otherwise similar to the cryptophytes. The other sketches portray the four major kinds of cell in the living world and their membrane topology. The upper ones show the contrasting ancestral microtubular cytoskeleton (ciliary roots, in red) of unikonts (a cone of single microtubules attaching the single centriole to the nucleus, blue) and bikonts (two bands of microtubules attached to the posterior centriole and an anterior fan of microtubules attached to the anterior centriole). The lower ones show the single plasma membrane of unibacteria (posibacteria plus archaebacteria), which were ancestral to eukaryotes and the double envelope of negibacteria, which were ancestral to mitochondria and chloroplasts (which retained the outer membrane, red). source: http://aob.oxfordjournals.org/cg i/content/full/95/1/147/FIG2
[2] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group. source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703 | |
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1,960,000,000 YBN 3 4 | 321) Rhizaria Phylum "Foraminifera" evolve now.1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). has 1600mybn for excavates, discricristales, rhizaria, chromalveolates 2. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). has 1600mybn for excavates, discricristales, rhizaria, chromalveolates (1600mybn) 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). |
[1] FIG. 2. The tree of life based on molecular, ultrastructural and palaeontological evidence. Contrary to widespread assumptions, the root is among the eubacteria, probably within the double-enveloped Negibacteria, not between eubacteria and archaebacteria (Cavalier-Smith, 2002b); it may lie between Eobacteria and other Negibacteria (Cavalier-Smith, 2002b). The position of the eukaryotic root has been nearly as controversial, but is less hard to establish: it probably lies between unikonts and bikonts (Lang et al., 2002; Stechmann and Cavalier-Smith, 2002, 2003). For clarity the basal eukaryotic kingdom Protozoa is not labelled; it comprises four major groups (alveolates, cabozoa, Amoebozoa and Choanozoa) plus the small bikont phylum Apusozoa of unclear precise position; whether Heliozoa are protozoa as shown or chromists is uncertain (Cavalier-Smith, 2003b). Symbiogenetic cell enslavement occurred four or five times: in the origin of mitochondria and chloroplasts from different negibacteria, of chromalveolates by the enslaving of a red alga (Cavalier-Smith, 1999, 2003; Harper and Keeling, 2003) and in the origin of the green plastids of euglenoid (excavate) and chlorarachnean (cercozoan) algae-a green algal cell was enslaved either by the ancestral cabozoan (arrow) or (less likely) twice independently within excavates and Cercozoa (asterisks) (Cavalier-Smith, 2003a). The upper thumbnail sketch shows membrane topology in the chimaeric cryptophytes (class Cryptophyceae of the phylum Cryptista); in the ancestral chromist the former food vacuole membrane fused with the rough endoplasmic reticulum placing the enslaved cell within its lumen (red) to yield the complex membrane topology shown. The large host nucleus and the tiny nucleomorph are shown in blue, chloroplast green and mitochondrion purple. In chlorarachneans (class Chlorarachnea of phylum Cercozoa) the former food vacuole membrane remained topologically distinct from the ER to become an epiplastid membrane and so did not acquire ribosomes on its surface, but their membrane topology is otherwise similar to the cryptophytes. The other sketches portray the four major kinds of cell in the living world and their membrane topology. The upper ones show the contrasting ancestral microtubular cytoskeleton (ciliary roots, in red) of unikonts (a cone of single microtubules attaching the single centriole to the nucleus, blue) and bikonts (two bands of microtubules attached to the posterior centriole and an anterior fan of microtubules attached to the anterior centriole). The lower ones show the single plasma membrane of unibacteria (posibacteria plus archaebacteria), which were ancestral to eukaryotes and the double envelope of negibacteria, which were ancestral to mitochondria and chloroplasts (which retained the outer membrane, red). source: http://aob.oxfordjournals.org/cg i/content/full/95/1/147/FIG2
[2] Fig. 1. A consensus phylogeny of eukaryotes. The vast majority of characterized eukaryotes, with the notable exception of major subgroups of amoebae, can now be assigned to one of eight major groups. Opisthokonts (basal flagellum) have a single basal flagellum on reproductive cells and flat mitochondrial cristae (most eukaryotes have tubular ones). Eukaryotic photosynthesis originated in Plants; theirs are the only plastids with just two outer membranes. Heterokonts (different flagellae) have a unique flagellum decorated with hollow tripartite hairs (stramenopiles) and, usually, a second plain one. Cercozoans are amoebae with filose pseudopodia, often living with in tests (hard outer shells), some very elaborate (foraminiferans). Amoebozoa are mostly naked amoebae (lacking tests), often with lobose pseudopodia for at least part of their life cycle. Alveolates have systems of cortical alveoli directly beneath their plasma membranes. Discicristates have discoid mitochondrial cristae and, in some cases, a deep (excavated) ventral feeding groove. Amitochondrial excavates lack substantial molecular phylogenetic support, but most have an excavated ventral feeding groove, and all lack mitochondria. The tree shown is based on a consensus of molecular (1-4) and ultrastructural (16, 17) data and includes a rough indication of new ciPCR ''taxa'' (broken black lines) (7-11). An asterisk preceding the taxon name indicates probable paraphyletic group. source: http://www.sciencemag.org/cgi/co ntent/full/300/5626/1703 | |
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1,900,000,000 YBN 3 4 | 66) Oldest Acritarch (eucaryote) fossils.1 2 FOOTNOTES 1. ^ http://www.ucl.ac.uk/GeolSci/micropal/ac ritarch.html 2. ^ Knoll AH (1992) The early evolution of eukaryotes: a geological perspective. Science 256: 622-627 3. ^ http://www.ucl.ac.uk/GeolSci/micropal/ac ritarch.html 4. ^ Knoll AH (1992) The early evolution of eukaryotes: a geological perspective. Science 256: 622-627 |
[1] Figure 1 Protistan microfossils from the Roper Group. a, c, Tappania plana, showing asymmetrically distributed processes and bulbous protrusions (arrow in a). b, detail of a, showing dichotomously branching process. d, Valeria lophostriata. e, Dictyosphaera sp. f, Satka favosa. The scale bar in a is 35 µm for a and c; 10 µm for b; 100 µm for d; 15 µm for e; and 40 µm for f. source: Nature 412
[2] Diagram showing basic morphological classification of acritarchs. COPYRIGHTED source: http://www.ucl.ac.uk/GeolSci/mic ropal/acritarch.html | |
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1,874,000,000 YBN | 61) Oldest non-acritarch Eukaryote fossil Grypania spiralis (an alga 10 cm long) from BIF in Michigan. Oldest algae fossil. 1 2 FOOTNOTES 1. ^ Han and Runnegar 1992. T.-M. Han and B. Runnegar, Megascopic eukaryotic algae from the 2.1-billion-year-old Negaunee Iron-Formation, Michigan. Science 257 (1992), pp. 232-235 science_2100_han_runnegar_algal _cysts.pdf 2. ^ Schneider et al 2002. D.A. Schneider, M.E. Bickford, W.F. Cannon, K.J. Schulz and M.A. Hamilton, Age of volcanic rocks and syndepositional iron formations, Marquette Range Supergroup; implications for the tectonic setting of Paleoproterozoic iron formations of the Lake Superior region. Can. J. Earth Sci. 39 6 (2002), pp. 999-1012. |
source: file:/root/web/Grypania_spiralis _wmel0000.htm
source: http://www.peripatus.gen.nz/pale ontology/lrgGrypaniaspiralis.jpg | |
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1,800,000,000 YBN | 46) End of the Banded Iron Formation Rocks.1 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). |
source: | |
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1,576,000,000 YBN 2 | 67) A eukaroyte cell forms a symbiotic relationship with cyanobacteria, which form plastids (chloroplasts). Like mitochondria, these organelles copy themselves and are not made by the cell DNA.1 FOOTNOTES 1. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 2. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002)., see comments | ||
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1,513,000,000 YBN 3 4 | 221) First fungi evolve.1 2 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1513mybn) 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c1200) | ||
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1,500,000,000 YBN 3 4 | 323) First plant (single cell, similar to glaucophytes) evolves.1 2 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1609 mybn) 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c1500) | ||
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1,400,000,000 YBN 4 5 6 | 86) Glaucophyta evolve.1 2 3 FOOTNOTES 1. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). 4. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849 (2002); doi:10.1038/nrg929, (2002). (c1500my) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c1400) 6. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). (1558my) |
[1] ? COPYRIGHTED source: http://protist.i.hosei.ac.jp/PDB 3/PCD3711/htmls/86.html
[2] ? COPYRIGHTED source: http://protist.i.hosei.ac.jp/PDB /Images/Others/Glaucocystis/ | |
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1,400,000,000 YBN 3 | 197) Opisthokonts (posterior cilium) evolve from Unikonts (ancestrally only one cilium). Opisthokonts have flat mitochondrial cristae and go on to form the Animal and Fungi kingdoms.1 2 FOOTN OTES 1. ^ J Mol Evol (2003) 56:540 563 Phylogeny of Choanozoa, Apusozoa, and Other Protozoa and Early Eukaryote Megaevolution Thomas Cavalier-Smith, Ema E.-Y. Chao /home/ted/ulsf/docs/cav-smith_apusozoa _fulltext.html 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). |
[1] cavalier-smith diagram COPYRIGHTED source: cavalier_jmolevol_2003_56_540-56 3.pdf
[2] Figure 1. Phylogenetic hypothesis of the eukaryotic lineage based on ultrastructural and molecular data. Organisms are divided into three main groups distinguished by mitochondrial cristal shape (either discoidal, flattened or tubular). Unbroken lines indicate phylogenetic relationships that are firmly supported by available data; broken lines indicate uncertainties in phylogenetic placement, resolution of which will require additional data. Color coding of organismal genus names indicates mitochondrial genomes that have been completely (Table 1), almost completely (Jakoba, Naegleria and Thraustochytrium) or partially (*) sequenced by the OGMP (red), the FMGP (black) or other groups (green). Names in blue indicate those species whose mtDNAs are currently being sequenced by the OGMP or are future candidates for complete sequencing. Amitochondriate retortamonads are positioned at the base of the tree, with broken arrows denoting the endosymbiotic origin(s) of mitochondria from a Rickettsia-like eubacterium. Macrophar., Macropharyngomonas. source: unknown | |
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1,400,000,000 YBN 3 4 | 220) Amoebozoa (amoeba, slime molds) evolve now.1 2 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1587mybn) 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c1400) |
[1] SUBPHYLUM Lobosa CLASS Amoebaea Chaos diffluens, an amoeba. Photo released by Dr. Ralf Wagner. source: http://en.wikipedia.org/wiki/Ima ge:Chaos_diffluens.jpg
[2] CLASS Amoebaea Mayorella (may-or -ell-a) a medium sized free-living naked amoeba with conical pseudopodia. Central body is the nucleus. Phase contrast. This picture was taken by David Patterson of material from Limulus-ridden sediments at Plum Island (Massachusetts USA) in spring and summer, 2001. NONCOMMERCIAL USE source: http://microscope.mbl.edu/script s/microscope.php?func=imgDetail&imageID= 515 | |
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1,300,000,000 YBN 7 8 9 10 11 | 188) Green Algae, composed of the 2 Phlya Chlorophyta (volvox, sea lettuce) and Charophyta (Spirogyra) evolve. 1 2 3 4 5 6 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 4. ^ Daniel S. Heckman,1 David M. Geiser,2 Brooke R. Eidell,1 Rebecca L. Stauffer,1 Natalie L. Kardos, "Molecular Evidence for the Early Colonization of Land by Fungi and Plants", Science 10 August 2001: Vol. 293. no. 5532, pp. 1129 - 1133 DOI: 10.1126/science.1061457, (2001). 5. ^ M. J. Benton, "The Fossil Record 2", (London; New York: Chapman & Hall, 1993). fr2b 6. ^ http://www.ucmp.berkeley.edu/greenalgae/ greenalgae.html 7. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (968mybn) 8. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1300mybn) 9. ^ Daniel S. Heckman,1 David M. Geiser,2 Brooke R. Eidell,1 Rebecca L. Stauffer,1 Natalie L. Kardos, "Molecular Evidence for the Early Colonization of Land by Fungi and Plants", Science 10 August 2001: Vol. 293. no. 5532, pp. 1129 - 1133 DOI: 10.1126/science.1061457, (2001). (1061?) 10. ^ M. J. Benton, "The Fossil Record 2", (London; New York: Chapman & Hall, 1993). fr2b (1650-800mybn) 11. ^ http://www.ucmp.berkeley.edu/greenalgae/ greenalgae.html (1000my) |
[1] Micrograph of Volvox aureus. Copyright held by Dr. Ralf Wagner, uploaded to German Wikipedia under GFDL. Permission is granted to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.2 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts. Subject to disclaimers. source: http://en.wikipedia.org/wiki/Vol vox
[2] Photo of green algal growth (Enteromorpha sp.) on rocky areas of the ocean intertidal shore, indicating a nearby nutrient source (in this case land runoff). Photographed by Eric Guinther near Kahuku, O'ahu, Hawai'i. GFDL Permission is granted to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.2 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts Subject to disclaimers source: http://en.wikipedia.org/wiki/Ima ge:Intertidal_greenalgae.jpg | |
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1,300,000,000 YBN 3 4 | 209) Red Algae (Rhodophyta) evolve now.1 2 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1428mybn) 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1300mybn) |
[1] Close-up of a red alga (Genus? Laurencia), Class Florideophyceae, Order=? a marine seaweed from Hawaii. GNU source: http://en.wikipedia.org/wiki/Ima ge:Laurencia.jpg
[2] Bangia atropurpurea Profile: unbranched filaments in tufts. Often forming dense fringes in the spalsh zone. Uniseriate at base, multiseriate above with protoplasts separate in a firm gelatinous sheath. Stellate chloroplasts. US NOAA PD source: http://www.glerl.noaa.gov/seagra nt/GLWL/Algae/Rhodophyta/Cards/Bangia.ht ml | |
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1,280,000,000 YBN 4 | 187) A eukaryote rhodophyte (red alga) is enslaved by a chromealveolate eukaryote to form a plastid in the chromealveolate. This kind of plastid is presumably inherited by all other chromalveolates (brown algae, diatoms, water molds, Dinoflagellata, Apicomplexa, ciliates) that have plastids.1 2 3 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ THOMAS CAVALIER-SMITH, "Economy, Speed and Size Matter: Evolutionary Forces Driving Nuclear Genome Miniaturization and Expansion", * Oxford Journals * Life Sciences * Annals of Botany * Volume 95, Number 1 *, (2005). 3. ^ Cavalier-Smith image from paper - have to find source but file:///home/ted/ulsf/docs/rooting_euk_t ree_cav-smith_science.html or THOMAS CAVALIER-SMITH, "Economy, Speed and Size Matter: Evolutionary Forces Driving Nuclear Genome Miniaturization and Expansion", * Oxford Journals * Life Sciences * Annals of Botany * Volume 95, Number 1 *, (2005). are similar 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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1,250,000,000 YBN 3 | 201) Oldest widely accepted Rhodophyta (red algae) fossils (Bangiomorpha pubescens) from Hunting Formation, Somerset Island, arctic Canada. 1 2 FOO TNOTES 1. ^ Science 1990 vol 250 Butterfield N. J. A. H. Knoll K. Swett 1990 A bangiophyte red alga from the Proterozoic of Arctic Canada. Science 250: 104-107 2. ^ Paleobiology Volume 26, Issue 3 (September 2000) http://www.bioone.org/perlserv/?r equest=get-document&doi=10.1666%2F0094-8 373%282000%29026%3C0386%3ABPNGNS%3E2.0.C O%3B2 3. ^ Science 1990 vol 250 Butterfield N. J. A. H. Knoll K. Swett 1990 A bangiophyte red alga from the Proterozoic of Arctic Canada. Science 250: 104-107 |
[1] get images from Life on a Young Planet, Knoll source: Science 1990 vol 250 Butterfield N. J. A. H. Knoll K. Swett 1990 A bangiophyte red alga from the Proterozoic of Arctic Canada. Science 250: 104-107[ISI][Medline]
[2] Figure 2. Griffithsia pacifica (Florideophyceae). Electron micrograph showing cytoplasm with numerous chloroplasts (C) and starch (S). Starch is the photosynthetic reserve and is deposited free in the cytoplasm. source: (American Journal of Botany. 2004;91:1494-1507.) | |
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1,100,000,000 YBN 3 4 | 75) Most ancient living fungi phylum "Microsporidia" evolves.1 2 FOOTNOTES 1. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849 (2002); doi:10.1038/nrg929, (2002). (>1460mybn) 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c1100mybn) MORE INFO [1] http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=93911 |
[1] Sporoblast of the Microsporidium Fibrillanosema crangonycis. Electron micrograph taken by Leon White. GNU source: http://en.wikipedia.org/wiki/Ima ge:Fibrillanosema_spore.jpg
[2] Spironema multiciliatum Spironema: Octosporoblastic sporogony producing horseshoe-shaped monokaryotic spores in sporophorous vesicles; monomorphic, diplokaryotic and monokaryotic; merogony - last generation merozoites are diplokaryotic; sporogony - initial division of the sporont nuclei is meiotic as indicated by the occurrence of synaptonemal complexes; spores are horse-shoe-shaped, with swollen ends in T. variabilis and have one elongate nucleus; exospore with three layers, endospore is of medium thickness; polaroplast composed of two lamellar parts, an anterior part of closely packed lamellae and a posterior part of wider compartments; polar tube is isofilar and forms, in the posterior quarter of the spore, 3-4 coils in a single rank (T. variabilis) or 8-10 coils in a single rank (T. chironomi); type species Toxoglugea vibrio in adipose tissue of larvae of Ceratopogon sp. (Diptera, Ceratopogonidae). Spironema (spire-oh-knee-ma) multiciliatum Klebs, 1893. Cells are lanceolate, relatively flattened and flexible. The cells have a spiral groove, long kinetics and a tail, which tapers posteriorly, and are about 15 - 21 microns without the tail. The nucleus is located anteriorly or near the centre of the cell. When the cells are squashed, the cells are more flexible. Food materials are seen under the cell surface. Rarely observed. This picture was taken by Won Je Lee using conventional photographic film using a Zeiss Axiophot microscope of material collected in marine sediments of Botany Bay (Sydney, Australia). The image description refers to material from Botany Bay. NONCOMMERCIAL USE source: http://microscope.mbl.edu/script s/microscope.php?func=imgDetail&imageID= 3928 | |
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1,000,000,000 YBN 3 4 | 223) Fungi phylum "Chytridiomycota" evolves.1 2 FOOTNOTES 1. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849 (2002); doi:10.1038/nrg929, (2002). (1460mybn) 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1000mybn) MORE INFO [1] http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=71577&tree=0.1 [2] http://en.wikipedia.org/wiki/Chytridiomy cota |
[1] Chytrids (Chytridiomycota): The Primitive Fungi These fungi are mostly aquatic, are notable for having a flagella on the cells (a flagella is a tail, somewhat like a tail on a sperm or a pollywog), and are thought to be the most primitive type of fungi. actual photo comes from: http://www.csupomona.edu/~jcclark /classes/bot125/resource/graphics/chy_al l_sph.html source: http://www.davidlnelson.md/Cazad ero/Fungi.htm
[2] Chytridiomycota - Blastocladiales - zoospore of Allomyces (phase contrast illumination) X 2000 source: http://www.mycolog.com/chapter2b .htm | |
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1,000,000,000 YBN 2 | 324) Phylum Choanozoa (Mesomycetozoea/DRIPs, Choanoflagellates) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). moved to 1000my from 1200 (Dawkins) 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). moved to 1000my from 1200 (Dawkins) | ||
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1,000,000,000 YBN | 325) The Choanozoan "Mesomycetozoaea" (DRIPs) evolve. 1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). |
[1] Ichthyophonus, a fungus-like protistan that occurs in high prevalence in Pacific Ocean perch (Sebastes aultus) and yellowtail rockfish (Sebastes flavedus). Note the parasite forms branching hyphae-like structures. Ichthyophonus hoferi has caused massive mortalities in herring in the Atlantic ocean, and has recently been reported to cause disease in wild Pacific herring from Washington through Alaska. COPYRIGHTED EDU source: http://oregonstate.edu/dept/salm on/projects/images/16Ichthyophonus.jpg
[2] Microscopic appearence of the organism is dependent on its stage of development. The stages include (1) spore at ''resting'' stage, (2) germinating spore, (3) hyphal stage. It is believed that there are two forms of Ichthyophonus, both belonging to one genus. One of them is known as the ''salmon'' form, occuring in freshwater and cold-preferring sea fishes: this form is characterized by its ability to produce long tubulose germ hyphae. The other is called the ''aquarium fish'' form, typical of the tropical freshwater fishes. This form is completely devoid of hyphae. Developmental cycle of Ichthyophonus hoferi: 1-5 - development of ''daughter'' spores, 7-11 - development of resting spore from the ''daughter'' spore, 12-19 - development of resting spore by fragmentation. COPYRIGHTED source: http://www.fao.org/docrep/field/ 003/AC160E/AC160E02.htm | |
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967,000,000 YBN 1 | 97) A lens and light sensitive area evolve in unicellular eukaryote living objects. This is the first proto eye. FOOTN OTES 1. ^ http://www.sidwell.edu/us/science/vlb5/L abs/Classification_Lab/Eukarya/Protista/ Euglenozoa/ | ||
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900,000,000 YBN 7 8 | 326) The Choanozoans "Choanoflagellates" and "Acanthoecida" evolve. 1 2 3 4 5 6 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=114293 3. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 4. ^ http://microscope.mbl.edu/scripts/protis t.php?func=integrate&myID=P2691&chinese_ flag=&system=&version=&documentID=&exclu deNonLinkedIn=&imagesOnly= 5. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1513 (drips?) and 1450 choano) 6. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1000 drips and 900 choano) 7. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1513 (drips?) and 1450 choano) 8. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1000 drips and 900 choano) |
[1] DOMAIN Eukaryota - eukaryotes KINGDOM Protozoa (Goldfuss, 1818) R. Owen, 1858 - protozoa SUBKINGDOM Sarcomastigota (means=?) PHYLUM Choanozoa CLASS Choanoflagellatea (Choanoflagellates and Acanthoecida) ORDER Acanthoecida Saepicula: Cells solitary, lorica funnel-shaped, 2 chambers delimited by a waist; constructed of rod-shaped costal strips; posterior chamber obconical with 2 series of costae located more or less regularly around chamber, one series almost parallel to the long axis of cell and second series almost perpendicular to long axis; anterior chamber formed by ring of equally spaced longitudinal costae surmounted by single transverse costa; marine This image is based on a drawing provided by Won Je Lee. NONCOMMERCIAL USE source: http://microscope.mbl.edu/script s/microscope.php?func=imgDetail&imageID= 3229
[2] Choanoeca: Cells solitary with distinct, firm flask-shaped theca more or less closely investing protoplast, with short pedicel; collar relatively long, widely expanded; flagellum absent in adult, but produced prior to cell division for locomotory use by juvenile cell; in marine and brackish habitats, frequently attached to filamentous algae and hydrozoa Choanoeca (ko-an-o-eek-a), an unusual loricate collar flagellate (choanoflagellate) in that the usual form is without a flagellum. Flagellated motile stage is occasionally produced. Widely dispersed pseudopodial elements of the collar are evident in this image. Differential interference contrast. This picture was taken by David Patterson and Aimlee Laderman of material collected from a freshwater Atantic white cedar swamp at Cumloden near Woods Hole in Massachusetts, USA in spring and summer, 2001. NONCOMMERCIAL USE source: http://microscope.mbl.edu/script s/microscope.php?func=imgDetail&imageID= 170 | |
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855,000,000 YBN 3 4 5 | 286) A key step in metazoan multicellularity evolves, where a zygote produces differentiated cells that stick together to form one organism.1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c850my) 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1351my) 5. ^ Ted Huntington, compromise between Dawkins and Hedges, et al. (compromise=1055) | ||
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850,000,000 YBN 4 5 6 | 81) First animal and first metazoan evolve. Metazoans are multicellular, but their cells perform different functions and originate from one cell(?). This is`also the beginning of the Animal Subkingdom "Radiata", species with radial symmetry. These are the sponges. There are only 3 kinds of metazoans: sponges, cnidarians, and bilaterians (which include all insects and vertibrates). Sponges are the first organisms whose DNA codes for more than one kind of cell. Sponges have 3 different cell types. Some cells form a body wall, some digest food, some form a skeletal frame.1 2 3 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c850my) 5. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1351my) 6. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). (600?) |
[1] source: http://www.museums.org.za/bio/me tazoa.htm
[2] source: http://www.museums.org.za/bio/me tazoa.htm | |
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850,000,000 YBN 2 | 101) First homeobox, or "hox" genes evolve. These genes regulate the building of major body parts.1 FOOTNOTE S 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 2. ^ same as sponge | ||
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850,000,000 YBN 5 6 7 8 | 224) Genetic comparison shows Fungi division "Zygomycota" (bread molds, pin molds, microsporidia,...) evolving now.1 2 3 4 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ Daniel S. Heckman,1 David M. Geiser,2 Brooke R. Eidell,1 Rebecca L. Stauffer,1 Natalie L. Kardos, "Molecular Evidence for the Early Colonization of Land by Fungi and Plants", Science 10 August 2001: Vol. 293. no. 5532, pp. 1129 - 1133 DOI: 10.1126/science.1061457, (2001). 3. ^ S. Blair Hedges and Sudhir Kumar, "Genomic clocks and evolutionary timescales", Trends in Genetics Volume 19, Issue 4 , April 2003, Pages 200-206, (2003). 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 5. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1250mybn) 6. ^ Daniel S. Heckman,1 David M. Geiser,2 Brooke R. Eidell,1 Rebecca L. Stauffer,1 Natalie L. Kardos, "Molecular Evidence for the Early Colonization of Land by Fungi and Plants", Science 10 August 2001: Vol. 293. no. 5532, pp. 1129 - 1133 DOI: 10.1126/science.1061457, (2001). (1107mybn) 7. ^ S. Blair Hedges and Sudhir Kumar, "Genomic clocks and evolutionary timescales", Trends in Genetics Volume 19, Issue 4 , April 2003, Pages 200-206, (2003). (1107mybn) 8. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c850m) |
[1] Figure 2. Zygomycota A: sporangia of Mucor sp. B: whorl of sporangia of Absidia sp. C: zygospore of Zygorhynchus sp. D: sporangiophore and sporangiola of Cunninghamella sp. source: http://www.botany.utoronto.ca/Re searchLabs/MallochLab/Malloch/Moulds/Cla ssification.html
[2] Figure 3. Syncephalis, a member of the Zygomycota parasitic on other Zygomycota source: http://www.botany.utoronto.ca/Re searchLabs/MallochLab/Malloch/Moulds/Cla ssification.html | |
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780,000,000 YBN 3 | 79) Animal Phylum "Placozoa" evolves.1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=11212&tree=0.1 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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750,000,000 YBN 2 | 83) Animal Phlyum Ctenophora (comb jellies) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c750) | ||
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750,000,000 YBN 4 5 6 | 225) Genetic comparison shows Fungi division "Glomeromycota" (Arbuscular mycorrhizal fungi) evolving now.1 2 3 F OOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 3. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c750mybn) 5. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849 (2002); doi:10.1038/nrg929, (2002). (c1460 to 1210mybn) 6. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (estimate that between 947 and 968) |
[1] germinating Gigaspora decipiens source: http://pages.unibas.ch/bothebel/ people/redecker/ff/glomero.htm
[2] Archaeospora leptoticha spores source: http://pages.unibas.ch/bothebel/ people/redecker/ff/glomero.htm | |
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700,000,000 YBN 4 5 6 | 82) First cnidarians (coelantrates), jellyfish evolves. Jellyfish have photon detecting cells and a lens made of ?.1 2 3 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 3. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 4. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). (580my) 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c700my) 6. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1298my) | ||
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700,000,000 YBN 4 5 6 | 226) The second largest group of Fungi, the phylum "Basidiomycota" (most mushrooms, rusts, club fungi) evolve.1 2 3 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (968my) 5. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849 (2002); doi:10.1038/nrg929, (2002). (1210my) 6. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (700my) |
[1] Amanita muscaria (Homobasidiomycetes) source: http://en.wikipedia.org/wiki/Ima ge:Agaricales.jpg
[2] Basidiomycete Life Cycle tjv source: http://botit.botany.wisc.edu/ima ges/332/Basidiomycota/General_basidio/Ba sidiomycete_Life_Cycle_tjv.php?highres=t rue | |
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700,000,000 YBN 4 5 6 | 227) The largest Fungi phylum "Ascomycota" (yeasts, truffles, Penicillium, morels, sac fungi) evolves.1 2 3 FOOTNOTES 1. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 2. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 4. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1009my) 5. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849 (2002); doi:10.1038/nrg929, (2002). (1140my) 6. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (700my) |
[1] white truffle cutted photographed by myself GNU head Permission is granted to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.2 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts. A copy of the license is included in the section entitled ''Text of the GNU Free Documentation License.'' source: http://upload.wikimedia.org/wiki pedia/commons/f/fd/Truffle_washed_and_cu tted.jpg
[2] EColi-Scerevisiae.jpg (50KB, MIME type: image/jpeg) Wikimedia Commons logo This is a file from the Wikimedia Commons. The description on its description page there is shown below. Escherichia coli (little forms) & Saccharomyces cerevisiae (big forms) by MEB Public domain This file has been released into the public domain by the copyright holder, its copyright has expired, or it is ineligible for copyright. This applies worldwide. brewer's yeast/baker's yeast source: http://en.wikipedia.org/wiki/Ima ge:EColi-Scerevisiae.jpg | |
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700,000,000 YBN 7 8 9 10 11 12 | 228) Genetic comparison shows the largest and second largest lines of Fungi (Ascomycota and Basidiomycota) splitting now.1 2 3 4 5 6 FOOTNOTES 1. ^ Daniel S. Heckman,1 David M. Geiser,2 Brooke R. Eidell,1 Rebecca L. Stauffer,1 Natalie L. Kardos, "Molecular Evidence for the Early Colonization of Land by Fungi and Plants", Science 10 August 2001: Vol. 293. no. 5532, pp. 1129 - 1133 DOI: 10.1126/science.1061457, (2001). 2. ^ S. Blair Hedges and Sudhir Kumar, "Genomic clocks and evolutionary timescales", Trends in Genetics Volume 19, Issue 4 , April 2003, Pages 200-206, (2003). 3. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 4. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 6. ^ Emmanuel J. P. Douzery, Elizabeth A. Snell, Eric Bapteste, Frédéric Delsuc, "The timing of eukaryotic evolution: Does a relaxed molecular clock reconcile proteins and fossils?", (PNAS) Proceedings of the National Academy of Sciences of the UNites States of America, (2001). 7. ^ Daniel S. Heckman,1 David M. Geiser,2 Brooke R. Eidell,1 Rebecca L. Stauffer,1 Natalie L. Kardos, "Molecular Evidence for the Early Colonization of Land by Fungi and Plants", Science 10 August 2001: Vol. 293. no. 5532, pp. 1129 - 1133 DOI: 10.1126/science.1061457, (2001). (1208my) 8. ^ S. Blair Hedges and Sudhir Kumar, "Genomic clocks and evolutionary timescales", Trends in Genetics Volume 19, Issue 4 , April 2003, Pages 200-206, (2003). (1208my) 9. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (968my) 10. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849 (2002); doi:10.1038/nrg929, (2002). (1210my) 11. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (700my) 12. ^ Emmanuel J. P. Douzery, Elizabeth A. Snell, Eric Bapteste, Frédéric Delsuc, "The timing of eukaryotic evolution: Does a relaxed molecular clock reconcile proteins and fossils?", (PNAS) Proceedings of the National Academy of Sciences of the UNites States of America, (2001). (727my) | ||
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630,000,000 YBN 5 6 | 91) First bilateral (has 2 sided symmetry) species evolves. Animal phylum Acoelomorpha (acoela flat worms and nemertodermatida) evolves. 1 2 3 Thi s begins the Subkingdom "Bilateria". 4 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=201049&tree=0.1 3. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 4. ^ http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=201049&tree=0.1 5. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (630my) 6. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). (575 (fossil is older) |
[1] Convoluta pulchra Smith and Bush 1991, a typical mud-inhabiting acoel that feeds on diatoms source: ? | |
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590,000,000 YBN 3 | 93) Protostomes evolve. Many phyla evolve at this time. Protostomes include the 3 infrakingdoms Ecdysozoa (a variety of worms and the arthropods {a huge group including all insects and crustaceans}), Platyzoa (rotifers and flatworms), and Lophotrochozoa (brachiopods {clams}, molluscs {snails}, and a variety of worms). 1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=198701 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (590my) | ||
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580,000,000 YBN | 94) Earliest animal fossil from Doushantuo formation in China.1 FOOTNOT ES 1. ^ http://biocrs.biomed.brown.edu/Books/Cha pters/Ch%2019/Fossil-Embryos/NYtimes-mic rofossils.html | ||
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580,000,000 YBN 2 | 165) Earliest bilaterian fossil, Vernanimalcula, 178 um in length, from Doushantuo Formation, China. First fossil of organism with bilateral symmetry, mouth, digestive track, gut and anus.1 FOOTNOTES 1. ^ Science, Vol 305, Issue 5681, 218-222, 9 July 2004 Small Bilaterian Fossils from 40 to 55 Million Years Before the Cambrian Jun-Yuan Chen,1,2* David J. Bottjer,3* Paola Oliveri,4 Stephen Q. Dornbos,3 Feng Gao,4 Seth Ruffins,4 Huimei Chi,5 Chia-Wei Li,6 Eric H. Davidson4 http://www.sciencemag.org/cgi/content/ full/sci;305/5681/218 2. ^ Science, Vol 305, Issue 5681, 218-222, 9 July 2004 Small Bilaterian Fossils from 40 to 55 Million Years Before the Cambrian Jun-Yuan Chen,1,2* David J. Bottjer,3* Paola Oliveri,4 Stephen Q. Dornbos,3 Feng Gao,4 Seth Ruffins,4 Huimei Chi,5 Chia-Wei Li,6 Eric H. Davidson4 http://www.sciencemag.org/cgi/content/ full/sci;305/5681/218 |
[1] Fig. 2. Close-up images of prominent anatomical features of Vernanimalcula guizhouena. The scale bar represents 18 µm in (A), 32 µm in (B), 24 µm in (C), and 28 µm in (D). SO, sensory organ, i.e., external pit; LU, lumen; PH, pharynx; MO, mouth; CO, coelomic lumen; CW, mesodermal coelomic wall; GU, gut. (A) Detail of collared mouth, multilayered pharynx, and one anterior surface pit. In this image, which is from the holotype specimen (Fig. 1A), the floor of the pit can be seen to be composed of a specialized concave layer. Note the coelomic wall, which here as elsewhere in these specimens has a thickness of about 5 to 6 µm. (B) Mouth of a fourth specimen, Q3105, displaying collared mouth and pharynx, ventral view. (C) Lumen of pharynx from a fifth specimen, X10419, secondarily encrusted but revealing morphology of opening of pharynx into gut similar to that seen in the specimens shown in Fig. 1. (D) Close-up of spaced external pits, interpreted as possible sensory organs, from the same specimen as shown in Fig. 1B [compare (A)]. source: http://www.sciencemag.org/cgi/co ntent/full/sci;305/5681/218
[2] Fig. 1. Images of three different, fairly well preserved specimens of the bilaterally organized fossil animal Vernanimalcula guizhouena. Left panels show digitally recorded, transmitted light images of sections about 50 µm thick, which had been ground from larger rock samples, mounted on slides, and viewed through a light microscope. Right panels show color-coded representations of the images on the left. These were prepared by digital image overlay. Yellow, external ectodermal layer; ochre, coelomic mesodermal layer; red, surface pits; mauve, pharynx; light tan, endodermal wall of gut; gray-green, lumen of mouth; dark gray, paired coelomic cavities; lighter gray, lumen of gut; brown, ''gland-like'' structures, with central lumen (B); light green, mineral inclusions (C). The scale bar represents 40 µm in (A), 55 µm in (B), and 46 µm in (C). (A) Holotype specimen, X00305, slightly tilted, almost complete ventral level coronal section, passing through the ventrally located mouth. (B) Coronal section of second specimen, X08981, passing through dorsal wall of pharynx and displaying complete A-P length of digestive tract, including posterior end [not visible in (A)]. (C) Tilted coronal section of third specimen, X10475, possibly slightly squashed, passing through dorsal wall of pharynx and through the dorsal wall of the gut. For dimensions, see Table 1. source: | |
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580,000,000 YBN 4 5 | 318) Protostome Infrakingdom Ecdysozoa evolves. Ecdysozoa are animals that molt (lose their outer skins) as they grow.1 2 Ecdysozoa include: the Phylum "Chaetognatha" (Arrow Worms), the Superphylum "Aschelminthes", containing the 5 Phlya: "Kinorhyncha" (kinorhynchs) "Loricifera" (loriciferans) "Nematoda" (round worms) "Nematomorpha" (horsehair worms), "Priapulida" (priapulids) the Superphlyum "Panarthropoda" containing the 3 Phyla: "Arthropoda" (arthropods: insects, shell fish) "Onychophora" (onychophorans) "Tardigrada" (tardigrades) 3 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 3. ^ http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=198710 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c580) 5. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). (560) | ||
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574,000,000 YBN 2 | 96) First neuron, nerve cell, and nervous system evolves in bilaterians.1 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). (presumably) 2. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). (presumably) | ||
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570,000,000 YBN | 95) Fluid filled cavity, coelom evolves in early bilaterians.1 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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570,000,000 YBN | 105) Deuterostomes evolve. This is the beginning of the Subkingdom Deuterostomia and Infrakingdom "Coelomopora" (Ambulacraria) with the two Phyla "Hemichordata" (acorn worms) and "Echinodermata" (sea cucumbers, sea urchins, starfish). 1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=198706 | ||
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570,000,000 YBN 2 | 311) Ecdysozoa phylum Chaetognatha (Arrow Worms) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (570) | ||
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570,000,000 YBN | 345) Deuterostome Coelomorpha Phylum Hemichordonia (acorn worms) evolves.1 F OOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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570,000,000 YBN | 346) Deuterostome Coelomorpha Phylum Echinodermata (sea cucumbers, sea urchins, sand dollars, star fish) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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565,000,000 YBN | 98) First circulatory system and red blood cells evolve in bilaterian worms.1 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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565,000,000 YBN 4 | 327) Infrakingdom Platyzoa (includes Superphylum Gnathifera {gnathiferans}, Phylum Gastrotricha {gastrotrichs}, and Phylum Platyhelminthes {flatworms}) evolve. 1 2 3 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=126691 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 4. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (565) | ||
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565,000,000 YBN | 347) Deuterostome Phylum Chordata evolves.1 Chordata is a very large group that contains all fish, amphibians, reptiles and mammals. FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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565,000,000 YBN | 348) Deuterstome Chordata Subphylum Tunicata (tunicates {sea squirts}) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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562,000,000 YBN | 99) Segmentation evolves.1 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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561,000,000 YBN | 100) Filter feeding, filtering food and oxygen from water through a digestive system, evolves in segmented worms.1 FO OTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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560,000,000 YBN 2 | 330) The two Ecdysozoa Superphyla Ashelminthes (round worms, horsehair worms, priapulids) and Pananthropoda (arthropods, onychophorans, tardigrades) separate. 1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c550) MORE INFO [1] http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=126686 | ||
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560,000,000 YBN | 349) Deuterstome Chordata Subphylum Cephalochordata (lancelets) evolves.1 This is the first fish. FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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550,000,000 YBN 3 | 328) Ecdysozoa Superphylum "Ashelminthes" evolves. This includes the 5 Phyla: Kinorhyncha (kinorhynchs), Loricifera (loriciferans), Nematoda (round worms), Nematomorpha (horsehair worms), Priapulida (priapulids). 1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=126691 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c550) | ||
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550,000,000 YBN 3 | 329) Platyzoa Superphylum "Gnathifera" evolves. This includes the 5 Phyla: Gna thostomulida (gnathostomulids), Cycliophora (cycliophorans), Micrognathozoa, Rotifera (rotifers), Acanthocephala (acanthocephalans). 1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=126686 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c550) | ||
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547,000,000 YBN 3 4 | 331) The Protostome Infrakingdom Lophotrochozoa evolves. This includes brachiopods, bryozoans, clams, squids and octopuses (cephalopods), and snails.1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Elizabeth Pennisi, "Drafting a Tree", Science, (2003). 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c547) 4. ^ Elizabeth Pennisi, "Drafting a Tree", Science, (2003). (550) | ||
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547,000,000 YBN 2 | 332) The Lophotrochozoa Superphylum Lophophorata evolves. This includes the two Phyla Phoronida (phoronids) and Brachiopoda (brachiopods {clams, oysters, muscles}).1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c547) | ||
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547,000,000 YBN 2 | 333) The Lophotrochozoa Phyla Phoronida (phoronids) evolves. 1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c547) | ||
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547,000,000 YBN 2 | 334) The Lophotrochozoa Phylum Brachiopoda (brachiopods {clams, oysters, muscles}) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c547) | ||
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545,000,000 YBN 2 | 335) The Lophotrochozoa Phylum Entoprocta (entoprocts) evolves.1 FOOTN OTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c545) | ||
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543,000,000 YBN | 53) End Precambrian Eon, start Phanerozoic Eon. End Proterozoic Era, start Paleozoic Era.1 2 FOOTNOTES 1. ^ The geological Society of America ucmp.berkeley.edu 2. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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543,000,000 YBN 2 | 104) The Platyzoa Phyla Platyhelminthes (flatworms) and Gastrotricha (gastrotrichs) evolve. 1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c543) | ||
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543,000,000 YBN | 120) Start Cambrian period (543-490 mybn).1 FOOTNOTES 1. ^ The geological Society of America | ||
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543,000,000 YBN 2 | 336) The Lophotrochozoa Phylum Bryozoa (Bryozoans or moss animals) evolves.1 F OOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c543) | ||
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543,000,000 YBN 2 | 337) The Ecdysozoa Superphylum Panarthropoda (Arthropods, Onychophora, Tardigrada) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c543) | ||
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543,000,000 YBN 2 | 338) The Ecdysozoa Phylum Arthropoda (insects, crustaceans) evolve.1 FOOTNOT ES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c543) | ||
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543,000,000 YBN 2 | 339) The Ecdysozoa Phylum Onychophora (onychophorans) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c543) | ||
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543,000,000 YBN 2 | 340) The Ecdysozoa Phylum Tardigrada (tardigrades) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c543) | ||
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542,000,000 YBN | 131) First shell (or skeleton) evolves.1 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). |
[1] Aldanella may be mollusc, if mollusc may be first known snail. shell is 1.5 mm in diameter. source: http://www.geology.ucdavis.edu/~ cowen/HistoryofLife/CH05images.html | |
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541,000,000 YBN 3 | 102) The Lophotrochozoa Superphylum Eutrochozoa (molluscs, ribbon, peanut, spoon, and segmented worms) evolves. 1 2 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ http://sn2000.taxonomy.nl/Taxonomicon/Ta xonTree.aspx?id=201563 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c541) | ||
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541,000,000 YBN | 132) Archaeocyatha (early sponges) evolve.1 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). |
[1] http://www.ucmp.berkeley.edu/porifera/ar chaeo.html source: http://www.ucmp.berkeley.edu/por ifera/archaeo.html
[2] http://www.geology.ucdavis.edu/~cowen/Hi storyofLife/CH05images.html source: http://www.geology.ucdavis.edu/~ cowen/HistoryofLife/CH05images.html | |
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541,000,000 YBN 2 | 341) The Lophotrochozoa Phylum Nemertea (ribbon worms) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c541) | ||
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540,000,000 YBN | 133) Earliest trilobite fossil.1 2 3 4 FOOTNOTES 1. ^ Xiao, S., Yang, Z. & Knoll, A. H. Nature 391, 553-558 (1998). Article ISI ChemPort http://www.nature.com/cgi-taf/DynaPage .taf?file=/nature/journal/v391/n6667/ful l/391553a0_fs.html (not clear that these are trilobite...this needs to be checked) 2. ^ http://www.nature.com/nature/journal/v42 7/n6971/full/427205a.html (here it is claimed they are trilobite embryos) 3. ^ science_266_5185_oldest_trilo.pdf has 510my 4. ^ http://www.ucmp.berkeley.edu/arthropoda/ trilobita/trilobitafr.html | ||
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539,000,000 YBN 2 | 342) The Lophotrochozoa Phylum Mollusca (brachiopods, bryozoans, clams, mussels, squids and octopuses {cephalopods}, and snails) evolves.1 FO OTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c539) | ||
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537,000,000 YBN 2 | 343) The Lophotrochozoa Phylum Annelida (segmented worms) evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c537) | ||
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537,000,000 YBN 2 | 344) The Lophotrochozoa Phylum Sipuncula (peanut worms) evolve.1 FOOTN OTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (c537) | ||
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530,000,000 YBN | 350) Deuterstome Chordata Subphylum Vertebrata evolves.1 This Subphylum contains most fish, all amphibians, reptiles, and mammals. FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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530,000,000 YBN | 351) Subphylum Vertebrata jawless fish (agnatha) evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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530,000,000 YBN 3 4 | 386) Oldest fossil vertebrate and fish.1 2 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm 2. ^ http://news.bbc.co.uk/1/hi/sci/tech/5047 76.stm 3. ^ http://www.uky.edu/KGS/education/timelin e2.htm 4. ^ http://news.bbc.co.uk/1/hi/sci/tech/5047 76.stm |
[1] Figure 4 The Lower Cambrian agnathan vertebrate Haikouichthys ercaicunensis Luo, Hu & Shu gen. et sp. nov. from Haikou, Yunnan. Specimen HZ-f-12-127. a, Entire specimen, anterior to the left; more posterior region appears to fade out into sediment, possibly representing decay of body; attempts to excavate this area were not successful. Scale bar equivalent to 5 mm. b, Detail of anterior to show putative gill bars, possible elements of cranial endoskeleton, and pericardic area; scale bar equivalent to 5 mm. c, Camera-lucida drawing of specimen to show interpretation. Numbers 1-6 indicate units of the branchial basket that are identified with some confidence; ?A-?C refer to less secure identifications. Two possible areas representing the pericardic cavity are indicated. To the anterior of ?C a triangular area with patches of diagenetic mineralization is one possibility; a fainter region to the posterior is the alternative location. COPYRIGHTED source: http://www.nature.com/nature/jou rnal/v402/n6757/fig_tab/402042a0_F4.html | |
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520,000,000 YBN | 205) Dinoflagellate biological markers measured in Kopli quarry, Tallinn, Estonia.1 2 FOOTNOTES 1. ^ Science, Vol 281, Issue 5380, 1168-1170 , 21 August 1998 2. ^ Biogeochemical Evidence for Dinoflagellate Ancestors in the Early Cambrian J. Michael Moldowan, * Nina M. Talyzina | ||
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507,000,000 YBN | 149) Marrella (Arthropod) fossils in Burgess Shale.1 2 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). 2. ^ http://www.nmnh.si.edu/paleo/shale/pmare lla.htm |
[1] diagram source: http://www.nmnh.si.edu/paleo/sha le/pmarella.htm
[2] fossil source: http://www.nmnh.si.edu/paleo/sha le/pmarella.htm | |
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490,000,000 YBN | 121) Start Ordovician (490-443 mybn), end Cambrian period (543-490 mybn).1 FO OTNOTES 1. ^ The geological Society of America | ||
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475,000,000 YBN 6 7 8 | 90) Genetic comparison shows the ancestor of all plants (Kingdom Plantae) evolving at this time (in the view that algae are protists and not plants).1 2 3 4 5 FOOTNOTES 1. ^ Seung Yeo Moon-van der Staay, Rupert De Wachter, Daniel Vaulot, "Oceanic 18S rDNA sequences from picoplankton reveal unsuspected eukaryotic diversity", Nature, (2001). 2. ^ Elizabeth Pennisi, "Drafting a Tree", Science, (2003). 3. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 4. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 5. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). 6. ^ S Blair Hedges, Jaime E Blair, Maria L Venturi and Jason L Shoe, "A molecular timescale of eukaryote evolution and the rise of complex multicellular life", BMC Evolutionary Biology 2004, 4:2 doi:10.1186/1471-2148-4-2, (2004). (1609my) 7. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). (1500) 8. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849 (2002); doi:10.1038/nrg929, (2002). (1580) |
source: http://protist.i.hosei.ac.jp/PDB 3/PCD3711/htmls/86.html
source: http://protist.i.hosei.ac.jp/PDB /Images/Others/Glaucocystis/ | |
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475,000,000 YBN 3 4 | 232) Genetic comparison shows the non-vascular plant and vascular plant lines splitting now.1 2 FOOTNOTES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). 3. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (c475) 4. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). (c475) | ||
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475,000,000 YBN 3 4 | 244) Genetic comparison shows non-vascular plants (Bryophytes) (Liverworts, Hornworts, Mosses) evolving now.1 2 FOOTNOTES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). 3. ^ S26 (c475) 4. ^ S15 (c475) |
[1] Phaeoceros laevis (L.) Prosk. gnu source: http://en.wikipedia.org/wiki/Ima ge:Anthoceros_levis.jpg
[2] Image of Phaeoceros (hornwort) spores taken by J. Ziffer. public domain source: wiki | |
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475,000,000 YBN | 352) Subphylum Vertebrata jawless fish lampreys and hagfish lines separate.1 F OOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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464,000,000 YBN | 398) Earliest fossil spore belonging to land plants. 1 FOOTNOTES 1. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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460,000,000 YBN | 353) Jawed vertebrates (Infraphylum Gnathostomata) evolve.1 This large group includes all jawed fish, all amphibians, reptiles, and mammals. FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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460,000,000 YBN | 354) Jawed vertebrate (Infraphylum Gnathostomata) Class Chondrichthyes (cartilaginous fishes) evolve.1 FOOTNOT ES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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450,000,000 YBN | 106) First chordates. The Chordata phylum includes all tunicates, fishes, amphibians, reptiles, birds, and mammals. The living chordate with the oldest DNA design are tunicates.1 FOOTN OTES 1. ^ Elizabeth Pennisi, "Drafting a Tree", Science, (2003). | ||
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443,000,000 YBN | 122) Start Silurian period (443-417), end Ordovician period (490-443 mybn).1 FOOTNOTES 1. ^ The geological Society of America | ||
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440,000,000 YBN 2 | 360) In the Jawed Fishes, the Ray-finned fishes (Subclass Actinopterygii) evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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428,000,000 YBN | 401) Oldest fossil of vascular land plants, Cooksonia. 1 2 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm 2. ^ M. J. Benton, "The Fossil Record 2", (London; New York: Chapman & Hall, 1993). |
[1] Cooksonia pertoni with three sporangia. Height of the plant 2.5 cm Pridolian (Upper Silurian) Shropshire, England. COPYRIGHTED source: http://www.xs4all.nl/~steurh/eng cook/ecookwal.html
[2] Cooksonia pertoni, fossilised plant COPYRIGHTED UK source: http://owen.nhm.ac.uk/piclib/web images/0/0/900/936_sml.jpg | |
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428,000,000 YBN | 402) Oldest fossil land animal, the millipede Pneumodesmus. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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425,000,000 YBN 2 | 377) Coelacanths evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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417,000,000 YBN | 123) Start Devonian period (417-354 mybn), end Silurian period (443-417 mybn).1 FOOTNOTES 1. ^ The geological Society of America | ||
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417,000,000 YBN 2 | 378) Lungfishes evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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412,000,000 YBN | 403) Oldest fossil lung fish. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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409,000,000 YBN | 404) Oldest fossil shark. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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400,000,000 YBN 3 4 | 236) Genetic comparison shows the oldest line of living vascular plants from the Division "Lycophyta" evolving now.1 2 FOOTNOTES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). 3. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (c400) 4. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). (c390) |
[1] Lycopodiella cernua (L.) Pic. Serm. plant from windward O'ahu (Hawai'i) taken in December 2003 by Eric Guinther and released under the GNU Free Documentation License. gnu source: http://en.wikipedia.org/wiki/Lyc ophyte
[2] Fossil trunk of Lepidodendron aculeatum showing leaf scars gnu source: http://en.wikipedia.org/wiki/Lep idodendron | |
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400,000,000 YBN | 399) Earliest fossil of an insect. 1 FOOTNOTES 1. ^ http://www.nhm.ac.uk/nature-online/earth /fossils/article-oldest-insect-fossil/th e-oldest-fossil-insect-in-the-world.html MORE INFO [1] http://www.nytimes.com/2004/02/11/scienc e/11CND-INSECT.html?ei=5007&en=01db2c70c 5f2bd18&ex=1391922000&adxnnl=1&partner=U SERLAND&adxnnlx=1146391843-YMWQeyxG2RWEx JKHKf60mQ |
[1] Rhyniognatha hirsti. COPYRIGHTED source: http://www.nhm.ac.uk/nature-onli ne/earth/fossils/article-oldest-insect-f ossil/the-oldest-fossil-insect-in-the-wo rld.html | |
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390,000,000 YBN | 355) Cartilaginous Fishes (Class Chondrichthyes) Subclass Subterbranchialia and Subclass Elasmobranchii (shark-like fishes) separate.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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390,000,000 YBN | 356) Subclass Subterbranchialia Superorder Holocephali (chimaeras: eg. elephant fish) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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380,000,000 YBN 3 4 | 243) Genetic comparison shows the Fern line and the line that leads to Seed Plants (Gymnosperms and Angiosperms) separating now.1 2 FOOTNOTES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). 3. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (318mybn) 4. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). (350mybn) | ||
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380,000,000 YBN 3 4 | 246) Genetic comparison shows the Spore producing and Seed producing plant lines separating now.1 2 FOOTNOTES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). 3. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (380mybn) 4. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). (350mybn) | ||
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380,000,000 YBN | 405) Oldest fossil large trees. First forests. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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380,000,000 YBN | 406) Oldest fossil spider. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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375,000,000 YBN | 407) Oldest fossil amphibian, and land vertebrate. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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360,000,000 YBN 3 4 | 237) Genetic comparison shows Ferns (Plant Division "Pteridophyta") evolving now.1 2 FOOTNOTES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). 3. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (c390 (360 for living species) 4. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). (c390) |
[1] Ferns, Melbourne Botanical Gardens gnu source: http://en.wikipedia.org/wiki/Fer n
[2] An Australian tree fern growing on O'ahu, Hawai'i. Photographed by Eric Guinther. A tree fern unrolling a new frond GNU source: same | |
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360,000,000 YBN | 408) Devonian mass extinction caused by ice age. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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354,000,000 YBN | 124) Start Carboniferous period (354-290 mybn), end Devonian period (417-354 mybn).1 FOOTNOTES 1. ^ The geological Society of America | ||
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350,000,000 YBN 2 | 361) In the Ray-finned fishes Superdivision Chondrostei (sturgeons and paddlefish) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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350,000,000 YBN 2 | 362) In the Ray-finned fishes Infradivsion Cladistia (Bichirs) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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340,000,000 YBN 2 | 379) Tetrapods evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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340,000,000 YBN 2 | 380) Amphibians (Caecillians, frogs, toads, Salamanders) evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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330,000,000 YBN | 409) Oldest fossil conifer. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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325,000,000 YBN 2 | 381) The Amphibians Caecillians evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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320,000,000 YBN 3 4 | 238) Genetic comparison shows the oldest living Gymnosperms from the Plant Kingdom evolving now.1 2 FOOTNOTE S 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). 3. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (c320 (360 for living species) 4. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). (c350 (300 for radiation) MORE INFO [1] "Gymnosperms". Wikipedia. Wikipedia, 2008. http://en.wikipedia.org/wiki/Gymnosperms |
[1] Leaves and female cone of Cycas revoluta GNU source: http://en.wikipedia.org/wiki/Cyc ad
[2] Leaves and male cone of Cycas revoluta Photo of Cycas (sago cycad) inflorescence, taken July 2001 by User:Stan Shebs Cycas revoluta - male plant GNU source: same | |
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318,000,000 YBN 3 4 | 242) Genetic comparison shows the Gymnosperms and Angiosperms lines separating now.1 2 FOOTNOTES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). 3. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (318mybn) 4. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). (350) | ||
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315,000,000 YBN | 410) Oldest fossil reptile. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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315,000,000 YBN | 411) Oldest fossil of flying insect (mayfly?). 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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315,000,000 YBN | 453) Allegheny mountains form as a result of the collision of Europe and eastern North America. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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310,000,000 YBN 2 | 384) Egg evolves.1
This group, the Amniota, will branch into the 3 major Classes: Reptiles (Sauropsida), Birds (Aves), and Mammals (Synapsida). FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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310,000,000 YBN 2 | 385) Reptiles evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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305,000,000 YBN 2 | 382) The Amphibians Frogs and Toads evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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305,000,000 YBN 2 | 383) Amphibians Salamanders evolve.1 FO OTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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300,000,000 YBN 2 | 387) Turtles, Tortoises and Terrapins evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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290,000,000 YBN | 125) Start Permian period (290-248 mybn), end Carboniferous period (354-290 mybn).1 FOOTNOTES 1. ^ The geological Society of America | ||
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280,000,000 YBN 2 | 388) Anapsids (iguanas and snakes) and diapsids (crocodiles) separate.1 FOOTNO TES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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260,000,000 YBN 2 | 363) In the Ray-finned fishes Infradivision Actinopteri evolves.1 FOO TNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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260,000,000 YBN 2 | 364) In the Ray-finned fishes Infradivision Actinopteri, Gars evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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255,000,000 YBN 2 | 389) Tuataras evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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251,000,000 YBN | 452) The supercontinent Pangea forms. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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250,000,000 YBN | 396) The Permian mass extinction event happens. 1 This is the most devastating mass extinction event in the history of earth. FOOTNOTES 1. ^ http://io.uwinnipeg.ca/~simmons/16cm05/1 116/16macro.htm meteor impact in antarctica: MORE INFO [1] http://www.sciencedaily.com/releases/200 6/06/060601174729.htm [2] http://www.ia.ucsb.edu/pa/display.aspx?p key=1073 |
[1] Timeloine of mass extinctions. COPYRIGHTED Benjamin Cummings. source: http://io.uwinnipeg.ca/~simmons/ 16cm05/1116/16macro.htm | |
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248,000,000 YBN | 54) End Paleozoic Era, start Mesozoic Era.1 2 FOOTNOTES 1. ^ The geological Society of America ucmp.berkeley.edu 2. ^ Richard Cowen, "History of Life", (Malden, MA: Blackwell, 2005). | ||
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248,000,000 YBN | 126) Start Triassic period (248-206 mybn), end Permian period (290-248 mybn).1 FOOTNOTES 1. ^ The geological Society of America | ||
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245,000,000 YBN 2 | 392) Crocodiles, allegators, caimans evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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245,000,000 YBN 2 | 393) Birds evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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240,000,000 YBN 2 | 365) Actinopteri Superdivision Neopterygii evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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240,000,000 YBN 2 | 366) In Superdivision Neopterygii, Subdivision Halecomorphi, Bow fish (Amiiformes) evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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240,000,000 YBN 2 | 367) Bow fish evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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228,000,000 YBN | 412) Oldest dinosaur fossil, Eorapter was found in South America. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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220,000,000 YBN | 400) Oldest mammal fossil. 1 FOOTNOTES 1. ^ http://www.abqtrib.com/albq/nw_science/a rticle/0,2668,ALBQ_21236_4546322,00.html | ||
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215,000,000 YBN | 428) Oldest Pterosaur fossil. 1 FOOTNOTES 1. ^ http://www.dinodata.net/DNM/dallav.htm | ||
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210,000,000 YBN 2 | 368) Subdivision Teleostei (eels, herrings, anchovies, carp, minnows, piranha, salmon, trout, pike, perch, seahorse, cod) evolves.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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210,000,000 YBN 2 | 369) Bonytongues evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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210,000,000 YBN 2 | 390) Iguanas, chamaeleons, spiny lizards evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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210,000,000 YBN 2 | 391) Snakes, Skinks, Geckos evolve.1 FO OTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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210,000,000 YBN | 413) Oldest turtle fossil. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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209,500,000 YBN 2 | 489) Triconodonta (extinct mammals) evolve. 1 FOOTNOTES 1. ^ "Triconodonta". Wikipedia. Wikipedia, 2008. http://en.wikipedia.org/wiki/Triconodont a 2. ^ http://www.biodiversity.org.uk/scripts/j ava/runjava.dll?java=BentonControlServer &method=jsShowStrat&family=Sinoconodonti dae | ||
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206,000,000 YBN | 127) Start Jurassic period (206-144 mybn), end Triassic period (248-206 mybn).1 FOOTNOTES 1. ^ The geological Society of America | ||
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200,000,000 YBN 2 | 370) Eels and tarpons (Elopocephala) evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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199,000,000 YBN | 414) End of Triassic mass extinction, because of climate (temperature?, weather?) changes. Large outpourings of lava from break-up of Pangea may have caused climate change. 1 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm | ||
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190,000,000 YBN | 357) Subclass Elasmobranchii (shark-like fishes) divides into 2 divisions Squalea (rays, skates) and Galeomorphii (great white, hammerhead, nurse, sand tiger sharks).1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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190,000,000 YBN 2 | 358) Division Squalea (rays, skates) evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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190,000,000 YBN 2 | 359) Division Galeomorphii (great white, hammerhead, nurse, sand tiger sharks) evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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190,000,000 YBN 2 | 371) Herrings and anchovies evolve.1 FO OTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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185,000,000 YBN 3 | 194) Oldest diatom (Heterokonts or Chromalveolates) fossils.1 2 FOOTNOTES 1. ^ Kooistra, W. H. C. F. and Medlin, L. K. (1996). Evolution of the diatoms (Bacillariophyta) : IV. A reconstruction of their age from small subunit rRNA coding regions and the fossil record. Mol. Phylogenet. Evol. 6, 391-407. 2. ^ "Diatom". Wikipedia. Wikipedia, 2008. http://en.wikipedia.org/wiki/Diatom 3. ^ Kooistra, W. H. C. F. and Medlin, L. K. (1996). Evolution of the diatoms (Bacillariophyta) : IV. A reconstruction of their age from small subunit rRNA coding regions and the fossil record. Mol. Phylogenet. Evol. 6, 391-407. MORE INFO [1] Round, F. E. and Crawford, R. M. (1990). The Diatoms. Biology and Morphology of the Genera, Cambridge University Press, UK. |
source: http://www.nature.com/news/2003/ 030217/images/diatom_180.jpg
source: http://www.ucmp.berkeley.edu/chr omista/diatoms/diatomdiverse.jpg | |
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180,000,000 YBN 2 | 456) First mammals, Monotremes evolves. 1 Monotremes lay eggs and are the oldest warm blooded species of record. FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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175,000,000 YBN 4 5 6 | 245) Genetic comparison shows the most ancient flowering plant (Angiosperm) still alive, "Amborella" evolving now.1 2 3 FOOTNOTES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). 3. ^ N Wikstrom, V Savolainen, MW Chase, "Evolution of the angiosperms: calibrating the family tree", Proc Biol Sci. 2001 Nov 7;268(1482):2211-20., (2001). 4. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (175mybn) 5. ^ Hwan Su Yoon, Jeremiah D. Hackett, Claudia Ciniglia, Gabriele Pinto and Debashish, "A Molecular Timeline for the Origin of Photosynthetic Eukaryotes", Molecular Biology and Evolution, (2004). (c100mybn) 6. ^ N Wikstrom, V Savolainen, MW Chase, "Evolution of the angiosperms: calibrating the family tree", Proc Biol Sci. 2001 Nov 7;268(1482):2211-20., (2001). (175mybn) MORE INFO [1] "Fruit". Wikipedia. Wikipedia, 2008. http://en.wikipedia.org/wiki/Fruit |
[1] Photo of Amborella trichopoda (Amborellaceae; photo © Sangtae Kim). source: http://tolweb.org/tree?group=ang iosperms
[2] none source: http://www.ucsc.edu/currents/99- 00/08-30/amborella.photo2.htm | |
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170,000,000 YBN 2 | 372) Carp, minnows, Piranhas evolve.1 F OOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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170,000,000 YBN 2 | 373) Salmon, Trout, Pike evolve.1 FOOTN OTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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150,000,000 YBN 2 | 374) Lightfish and Dragonfish evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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150,000,000 YBN | 394) Oldest bird fossil, Archaeopteryx.1 FOOTNOTES 1. ^ http://www.toyen.uio.no/palmus/galleri/m ontre/english/x499b.htm MORE INFO [1] http://www.netpets.org/birds/newsroom/ar chaeopteryx.html [2] http://www.palaeos.com/Vertebrates/Units /350Aves/100.html#Archaeornithes |
[1] Archaeopteryx siemensii HMN 1880/81 (Berlin) COPYRIGHTED EDU source: http://www.oucom.ohiou.edu/dbms- witmer/dinoskulls02.htm
[2] Archaeopteryx sp. JM 2257 (Eichstätt) COPYRIGHTED EDU source: http://www.oucom.ohiou.edu/dbms- witmer/dinoskulls02.htm | |
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150,000,000 YBN | 395) Bird Confuciusornis fossil. 1
Unlike Archaeopteryx, Confuciusornis had no teeth. FOOTNOTES 1. ^ http://www.ucmp.berkeley.edu/diapsids/bi rds/birdfr.html |
[1] Confuciusornis source: http://www.ucmp.berkeley.edu/dia psids/birds/confuciusornislg.jpg | |
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146,000,000 YBN 2 | 490) Multituberculata (extinct major branch of mammals) evolve. 1 FOOTNOTES 1. ^ "Multituberculata". Wikipedia. Wikipedia, 2008. http://en.wikipedia.org/wiki/Multituberc ulata 2. ^ http://www.biodiversity.org.uk/scripts/j ava/runjava.dll?java=BentonControlServer &method=jsShowStrat&family=Arginbaatarid ae | ||
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145,000,000 YBN | 415) Oldest flower fossil. 1 2 3 FOOTNOTES 1. ^ http://www.uky.edu/KGS/education/timelin e2.htm 2. ^ http://www.rgp.ufl.edu/publications/expl ore/v04n1/fossil1.html 3. ^ Science November 27, 1998 |
[1] Archaefructus liaoningensis. The leaf-like structures on the stem of this 140 million year old fossil are pods containing the seeds, a characteristic unique to flowering plants. Credit: University of Florida. PD? source: http://science.nasa.gov/headline s/y2001/ast17apr_1.htm?list118443
[2] Archaefructus liaoningensis Sun, Dilcher, Zheng et Zhou (Sun et al., 1998). Fruiting axes and remains of two subtending leaves (Photo courtesy of David Dilcher). COPYRIGHTED EDU source: http://www.flmnh.ufl.edu/deeptim e/virtualfossilcollection/Archaeofructus .html | |
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144,000,000 YBN | 128) Start Cretaceous period (144-65 mybn), end Jurassic period (206-144 mybn).1 FOOTNOTES 1. ^ The geological Society of America | ||
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140,000,000 YBN 2 | 457) Marsupials evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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140,000,000 YBN 1 | 458) Metornithes (early birds) evolve. FOOTNOTES 1. ^ http://www.palaeos.com/Vertebrates/Units /350Aves/350.200.html (estimate from) |
[1] Alvarezsaurid. COPYRIGHTED source: http://www.palaeos.com/Vertebrat es/Units/350Aves/350.200.html | |
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138,000,000 YBN 1 | 459) Ornithothoraces (early birds) evolve. FOOTNOTES 1. ^ http://www.palaeos.com/Vertebrates/Units /350Aves/350.500.html#Ornithothoraces (estimate from) | [1] Iberomesornis COPYRIGHTED, Iberomesornis COPYRIGHTED source: http://www.dinosauromorpha.de/th eropoda/iberomesornis.JPG
source: http://www.lemanlake.com/photos/ biotope/biodiversite/iberomesornis.gif | |
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136,000,000 YBN 1 | 460) Enantiornithes (early birds) evolve. FOOTNOTES 1. ^ http://www.palaeos.com/Vertebrates/Units /350Aves/350.500.html#Enantiornithes (estimate from) |
[1] Sinornis santensis Artist: James Reece COPYRIGHTED AUSTRALIA source: http://www.amonline.net.au/chine se_dinosaurs/feathered_dinosaurs/photo07 .htm | |
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134,000,000 YBN 1 | 461) Ornithurae (early birds) evolve. FOOTNOTES 1. ^ http://www.palaeos.com/Vertebrates/Units /350Aves/350.500.html#Ornithurae (estimate from) |
[1] fossil specimen of Chaoyangornis COPYRIGHTED source: http://www.sino-collector.com/en g/_private/cjyd/zjlt/hjs-hs/pic-l/hs0016 .jpg
[2] Chaoyangia, modified from Hou et al. (1996) COPYRIGHTED EDU source: http://rainbow.ldeo.columbia.edu /courses/v1001/clover16.html | |
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132,000,000 YBN 1 | 462) Hesperornithiformes (early birds) evolve. FOOTNOTES 1. ^ http://www.palaeos.com/Vertebrates/Units /350Aves/350.500.html#Hesperornithiforme s (estimate from) |
[1] Hesperornis. COPYRIGHTED source: http://www.savageancientseas.com /images/labels/hesperornis.jpg
[2] Detail of a painting by Ely Kish, Copyright © Ely Kish; used with permission of Ely Kish (EMAIL) Hesperornis regalis Hesperornis (pronounced HES-per-OR-nis) means ''western bird''. Toothed marine birds of the Late Cretaceous seas COPYRIGHTED source: http://www.oceansofkansas.com/He sperornis/kish-01.jpg | |
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130,000,000 YBN 2 | 375) Perch, Plaice, seahorses evolve.1 FOOTNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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130,000,000 YBN 2 | 376) Cod, hake, anglerfish evolve.1 FOO TNOTES 1. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). 2. ^ Richard Dawkins, "The Ancestor's Tale", (Boston, MA: Houghton Mifflin Company, 2004). | ||
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128,000,000 YBN 3 4 | 252) Genetic comparison shows the Angiosperm group "Monocotyledons" (Monocots) evolving now. Monocots are the second largest lineage of flowers after the Eudicots, and include lilies, palms, orchids, and grasses.1 2 FOOTNOT ES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ N Wikstrom, V Savolainen, MW Chase, "Evolution of the angiosperms: calibrating the family tree", Proc Biol Sci. 2001 Nov 7;268(1482):2211-20., (2001). 3. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (128mybn) 4. ^ N Wikstrom, V Savolainen, MW Chase, "Evolution of the angiosperms: calibrating the family tree", Proc Biol Sci. 2001 Nov 7;268(1482):2211-20., (2001). (153mybn) |
[1] Sweet Flag (Acorus calamus) - spadix Spadix of Sweet Flag. usgs public domain source: http://en.wikipedia.org/wiki/Aco rus
[2] Ivy Duckweed (Lemna trisulca) Name Lemna trisulca Family Lemnaceae source: http://en.wikipedia.org/wiki/Ali smatales | |
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128,000,000 YBN 3 4 | 253) Genetic comparison shows the Angiosperm group Eudicots (includes most former dicotyledons) evolving now. Eudicots are the largest lineage of flowers.1 2 FOOTNOTES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ N Wikstrom, V Savolainen, MW Chase, "Evolution of the angiosperms: calibrating the family tree", Proc Biol Sci. 2001 Nov 7;268(1482):2211-20., (2001). 3. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (128mybn) 4. ^ N Wikstrom, V Savolainen, MW Chase, "Evolution of the angiosperms: calibrating the family tree", Proc Biol Sci. 2001 Nov 7;268(1482):2211-20., (2001). (153mybn) | ||
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128,000,000 YBN 4 5 | 255) Genetic comparison shows the Angiosperm groups "Asterids" and "Rosids" evolving and separating now.1 2 3 FOOTNOTES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ N Wikstrom, V Savolainen, MW Chase, "Evolution of the angiosperms: calibrating the family tree", Proc Biol Sci. 2001 Nov 7;268(1482):2211-20., (2001). 3. ^ THE ANGIOSPERM PHYLOGENY GROUP*, "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II", Botanical Journal of the Linnean Society Volume 141 Page 399 - April 2003 doi:10.1046/j.1095-8339, (2003). 4. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (128mybn) 5. ^ N Wikstrom, V Savolainen, MW Chase, "Evolution of the angiosperms: calibrating the family tree", Proc Biol Sci. 2001 Nov 7;268(1482):2211-20., (2001). (122mybn) MORE INFO [1] wiki | ||
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128,000,000 YBN 3 4 | 266) Genetic comparison shows the Angiosperm "Monocotyledon" (Monocot) group "Commelinids" evolving now.1 2 FO OTNOTES 1. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 2. ^ N Wikstrom, V Savolainen, MW Chase, "Evolution of the angiosperms: calibrating the family tree", Proc Biol Sci. 2001 Nov 7;268(1482):2211-20., (2001). 3. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). (128mybn) 4. ^ N Wikstrom, V Savolainen, MW Chase, "Evolution of the angiosperms: calibrating the family tree", Proc Biol Sci. 2001 Nov 7;268(1482):2211-20., (2001). (153my) |
[1] Manila dwarf coconut palm from http://www.ars.usda.gov/is/graphics/phot os/ Manila dwarf coconut palm thumbnail A Manila dwarf coconut palm on the grounds of the Tropical Agriculture Research Station in Mayaguez, Puerto Rico. dept of ag public domain source: http://en.wikipedia.org/wiki/Are cales
[2] coconut GOV public domain source: http://www.nps.gov/kaho/KAHOckLs /KAHOplnt/images/IMG_03957.jpg | |
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128,000,000 YBN 5 6 | 267) Genetic comparison shows the Angiosperm "Core Eudicots" evolving now.1 2 3 4 FOOTNOTES 1. ^ THE ANGIOSPERM PHYLOGENY GROUP*, "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II", Botanical Journal of the Linnean Society Volume 141 Page 399 - April 2003 doi:10.1046/j.1095-8339, (2003). 2. ^ S. Blair Hedges, "The Origin and Evolution of Model Organisms", Nature Reviews Genetics 3, 838-849; doi:10.1038/nrg929, (2002). 3. ^ N Wikstrom, V Savolainen, MW Chase, "Evolution of the angiosperms: calibrating the family tree", Proc Biol Sci. 2001 Nov 7;268(1482):2211-20., (2001). 4. ^ Jeffrey D. Palmer, Douglas E. Soltis and Mark W. Chase, "The plant tree of life: an overview and some points of view", American Journal of Botany. 2004;91:1437-1445., (2004). 5. ^ Jeffrey D. Palme | ||