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How we'll resurrect the gastric brooding frog, the Tasmanian tiger

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    I do want to test this question we're all interested in:
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    Does extinction have to be forever?
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    I'm focused on two projects I want to tell you about.
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    One is the Thylacine Project.
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    The other one is the Lazarus Project,
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    and that's focused on the gastric brooding frog.
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    And it would be a fair question to ask, well,
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    why have we focused on these two animals?
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    Well, point number one, each of them
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    represents a unique family of its own.
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    We've lost a whole family.
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    That's a big chunk of the global genome gone.
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    I'd like it back.
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    The second reason is that we killed these things.
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    In the case of the thylacine, regrettably,
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    we shot every one that we saw. We slaughtered them.
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    In the case of the gastric brooding frog,
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    we may have "fungicided" it to death.
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    There's a dreadful fungus that's sort of moving
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    through the world that's called the chytrid fungus,
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    and it's nailing frogs all over the world.
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    We think that's probably what got this frog,
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    and humans are spreading this fungus.
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    And this introduces a very important ethical point,
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    and I think you will have heard this many times
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    when this topic comes up.
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    What I think is important is that,
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    if it's clear that we exterminated these species,
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    then I think we not only have a moral obligation
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    to see what we can do about it, but I think we've got
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    a moral imperative to try to do something, if we can.
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    Okay. Let me talk to you about the Lazarus Project.
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    It's a frog. And you think, frog.
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    Yeah, but this was not just any frog.
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    Unlike a normal frog, which lays its eggs in the water
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    and goes away and wishes its froglets well,
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    this frog swallowed its fertilized eggs,
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    swallowed them into the stomach where it should be having food,
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    didn't digest the eggs,
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    and turned its stomach into a uterus.
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    In the stomach, the eggs went on to develop into tadpoles,
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    and in the stomach, the tadpoles went on to develop into frogs,
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    and they grew in the stomach until eventually
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    the poor old frog was at risk of bursting apart.
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    It has a little cough and a hiccup, and out comes
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    sprays of little frogs.
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    Now, when biologists saw this, they were agog.
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    They thought, this is incredible.
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    No animal, let alone a frog, has been known to do this,
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    to change one organ in the body into another.
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    And you can imagine the medical world went nuts over this as well.
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    If we could understand how that frog is managing
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    the way its tummy works, is there information
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    here that we need to understand or could usefully use
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    to help ourselves?
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    Now, I'm not suggesting we want to raise our babies in our stomach,
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    but I am suggesting it's possible we might want
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    to manage gastric secretion in the gut.
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    And just as everybody got excited about it, bang!
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    It was extinct.
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    I called up my friend, Professor Mike Tyler
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    in the University of Adelaide.
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    He was the last person who had this frog,
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    a colony of these things, in his lab.
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    And I said, "Mike, by any chance -- "
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    this was 30 or 40 years ago —
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    "by any chance had you kept any frozen tissue of this frog?"
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    And he thought about it, and he went to his deep freezer,
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    minus 20 degrees centigrade,
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    and he poured through everything in the freezer,
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    and there in the bottom was a jar
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    and it contained tissues of these frogs.
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    This was very exciting, but there was no reason
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    why we should expect that this would work,
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    because this tissue had not had any antifreeze put in it,
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    cryoprotectants, to look after it when it was frozen.
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    And normally, when water freezes, as you know, it expands,
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    and the same thing happens in a cell.
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    If you freeze tissues, the water expands,
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    damages or bursts the cell walls.
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    Well, we looked at the tissue under the microscope.
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    It actually didn't look bad. The cell walls looked intact.
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    So we thought, let's give it a go.
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    What we did is something called
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    somatic cell nuclear transplantation.
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    We took the eggs of a related species, a living frog,
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    and we inactivated the nucleus of the egg.
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    We used ultraviolet radiation to do that.
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    And then we took the dead nucleus from the dead tissue
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    of the extinct frog and we inserted those nuclei into that egg.
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    Now by rights, this is kind of like a cloning project,
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    like what produced Dolly, but it's actually very different,
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    because Dolly was live sheep into live sheep cells.
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    That was a miracle, but it was workable.
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    What we're trying to do is take a dead nucleus from an extinct species
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    and put it into a completely different species and expect that to work.
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    Well, we had no real reason to expect it would,
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    and we tried hundreds and hundreds of these.
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    And just last February, the last time we did these trials,
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    I saw a miracle starting to happen.
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    What we found was, most of these eggs didn't work,
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    but then suddenly one of them began to divide.
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    That was so exciting. And then the egg divided again.
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    And then again. And pretty soon, we had
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    early stage embryos with hundreds of cells forming those.
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    We even DNA tested some of these cells,
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    and the DNA of the extinct frog is in those cells.
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    So we're very excited. This is not a tadpole.
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    It's not a frog. But it's a long way along the journey
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    to producing, or bringing back, an extinct species.
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    And this is news. We haven't announced this publicly before.
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    We're excited. We've got to get past this point.
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    We now want this ball of cells to start to gastrulate,
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    to turn in so that it will produce the other tissues.
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    It'll go on and produce a tadpole and then a frog.
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    Watch this space. I think we're going to have this frog
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    hopping glad to be back in the world again.
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    Thank you. (Applause)
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    We haven't done it yet, but keep those applause ready.
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    The second project I want to talk to you about is the Thylacine Project.
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    The thylacine looks a bit, to most people, like a dog,
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    or maybe like a tiger, because it has stripes.
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    But it's not related to any of those.
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    It's a marsupial. It raised its young in a pouch,
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    like a koala or a kangaroo would do,
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    and it has a long history, a long, fascinating history,
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    that goes back 25 million years.
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    But it's also a tragic history.
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    The first one that we see occurs in the ancient rainforests
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    of Australia about 25 million years ago,
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    and the National Geographic Society is helping us
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    to explore these fossil deposits. This is Riversleigh.
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    In those fossil rocks are some amazing animals.
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    We found marsupial lions.
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    We found carnivorous kangaroos.
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    It's not what you usually think about as a kangaroo,
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    but these are meat-eating kangaroos.
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    We found the biggest bird in the world,
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    bigger than that thing that was in Madagascar,
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    and it too was a flesh-eater. It was a giant, weird duck.
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    And crocodiles were not behaving at that time either.
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    You think of crocodiles as doing their ugly thing,
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    sitting in a pool of water.
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    These crocodiles were actually out on the land
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    and they were even climbing trees and jumping on prey
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    on the ground.
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    We had, in Australia, drop crocs. They really do exist.
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    But what they were dropping on was not only
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    other weird animals but also thylacines.
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    There were five different kinds of thylacines in those ancient forests,
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    and they ranged from great big ones to middle-sized ones
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    to one that was about the size of a chihuahua.
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    Paris Hilton would have been able to carry
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    one of these things around in a little handbag,
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    until a drop croc landed on her.
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    At any rate, it was a fascinating place,
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    but unfortunately, Australia didn't stay this way.
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    Climate change has affected the world for a long period of time,
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    and gradually, the forests disappeared,
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    the country began to dry out,
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    and the number of kinds of thylacines began to decline,
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    until by five million years ago, only one left.
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    By 10,000 years ago, they had disappeared
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    from New Guinea, and unfortunately
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    by 4,000 years ago, somebodies,
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    we don't know who this was, introduced dingoes --
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    this is a very archaic kind of a dog — into Australia.
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    And as you can see, dingoes are very similar
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    in their body form to thylacines.
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    That similarity meant they probably competed.
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    They were eating the same kinds of foods.
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    It's even possible that aborigines were keeping
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    some of these dingoes as pets, and therefore
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    they may have had an advantage in the battle for survival.
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    All we know is, soon after the dingoes were brought in,
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    thylacines were extinct in the Australian mainland,
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    and after that they only survived in Tasmania.
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    Then, unfortunately, the next sad part of the thylacine story
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    is that Europeans arrived in 1788, and they brought
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    with them the things they valued, and that included sheep.
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    They took one look at the thylacine in Tasmania,
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    and they thought, hang on, this is not going to work.
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    That guy is going to eat all our sheep.
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    That was not what happened, actually.
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    Wild dogs did eat a few of the sheep, but the thylacine got a bad rap.
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    But immediately, the government said, that's it,
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    let's get rid of them, and they paid people
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    to slaughter every one that they saw.
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    By the early 1930s, 3,000 to 4,000 thylacines
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    had been murdered. It was a disaster,
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    and they were about to hit the wall.
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    Have a look at this bit of film footage.
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    It makes me very sad, because, while, it's a fascinating animal,
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    and it's amazing to think that we had the technology to film it
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    before it actually plunged off that cliff of extinction,
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    we didn't, unfortunately, at this same time, have
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    a molecule of concern about the welfare for this species.
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    These are photos of the last surviving thylacine, Benjamin,
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    who was in the Beaumaris Zoo in Hobart.
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    To add insult to injury, having swept this species
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    nearly off the table, this animal, when it died of neglect,
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    the keepers didn't let it into the hutch
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    on a cold night in Hobart. It died of exposure,
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    and in the morning, when they found the body of Benjamin,
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    they still cared so little for this animal
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    that they threw the body in the dump.
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    Does it have to stay this way?
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    In 1990, I was in the Australian Museum.
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    I was fascinated by thylacines. I've always been obsessed with these animals.
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    And I was studying skulls, trying to figure out
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    their relationships to other sorts of animals,
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    and I saw this jar, and here, in the jar,
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    was a little girl thylacine pup, perhaps six months old.
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    The guy who had found it and killed the mother
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    had pickled the pup and they pickled it in alcohol.
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    I'm a paleontologist, but I still knew alcohol was a DNA preservative.
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    But this was 1990, and I asked my geneticist friends,
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    couldn't we think about going into this pup
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    and extracting DNA, if it's there,
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    and then somewhere down the line in the future,
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    we'll use this DNA to bring the thylacine back?
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    The geneticists laughed. But this was six years before Dolly.
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    Cloning was science fiction. It had not happened.
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    But then suddenly cloning did happen.
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    And I thought, when I became director
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    of the Australian Museum, I'm going to give this a go.
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    I put a team together.
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    We went into that pup to see what was in there,
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    and we did find thylacine DNA. It was a eureka moment.
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    We were very excited.
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    Unfortunately, we also found a lot of human DNA.
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    Every old curator who'd been in that museum
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    had seen this wonderful specimen,
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    put their hand in the jar, pulled it out and thought,
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    "Wow, look at that," plop, dropped it back in the jar,
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    contaminating this specimen.
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    And that was a worry. If the goal here was to get the DNA out
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    and use the DNA down the track to try to bring a thylacine back,
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    what we didn't want happening when the information
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    was shoved into the machine and the wheel turned around
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    and the lights flashed, was to have a wizened old
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    horrible curator pop out the other end of the machine. (Laughter)
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    It would've kept the curator very happy,
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    but it wasn't going to keep us happy.
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    So we went back to these specimens and we started digging around,
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    and particularly we looked into the teeth of skulls,
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    hard parts where humans had not been able to get their fingers,
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    and we found much better quality DNA.
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    We found nuclear mitochondrial genes. It's there.
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    So we got it.
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    Okay. What could we do with this stuff?
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    Well, George Church in his book, "Regenesis,"
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    has mentioned many of the techniques that are rapidly advancing
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    to work with fragmented DNA.
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    We would hope that we'll be able to get that DNA back
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    into a viable form, and then, much like we've done with the Lazarus Project,
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    get that stuff into an egg of a host species.
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    It has to be a different species.
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    What could it be? Why couldn't it be a Tasmanian devil?
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    They're related distantly to thylacines.
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    And then the Tasmanian devil is going to pop
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    a thylacine out the south end.
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    Critics of this project say, hang on.
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    Thylacine, Tasmanian devil? That's going to hurt.
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    No, it's not. These are marsupials.
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    They give birth to babies that are the size of a jelly bean.
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    That Tasmanian devil's not even going to know it gave birth.
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    It is, shortly, going to think it's got the ugliest
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    Tasmanian devil baby in the world,
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    so maybe it'll need some help to keep it going.
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    Andrew Pask and his colleagues have demonstrated
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    this might not be a waste of time.
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    And it's sort of in the future, we haven't got there yet,
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    but it's the kind of thing we want to think about.
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    They took some of this same pickled thylacine DNA
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    and they spliced it into a mouse genome,
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    but they put a tag on it so that anything
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    that this thylacine DNA produced
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    would appear blue-green in the mouse baby.
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    In other words, if thylacine tissues were being produced
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    by the thylacine DNA, it would be able to be recognized.
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    When the baby popped up, it was filled with blue-green tissues.
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    And that tells us if we can get that genome back together,
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    get it into a live cell, it's going to produce thylacine stuff.
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    Is this a risk?
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    You've taken the bits of one animal
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    and you've mixed them into the cell of a different kind of an animal.
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    Are we going to get a Frankenstein?
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    You know, some kind of weird hybrid chimera?
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    And the answer is no.
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    If the only nuclear DNA that goes into this hybrid cell
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    is thylacine DNA, that's the only thing that can pop out
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    the other end of the devil.
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    Okay, if we can do this, could we put it back?
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    This is a key question for everybody.
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    Does it have to stay in a laboratory,
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    or could we put it back where it belongs?
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    Could we put it back in the throne of the king of beasts
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    in Tasmania where it belongs, restore that ecosystem?
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    Or has Tasmania changed so much
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    that that's no longer possible?
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    I've been to Tasmania. I've been to many of the areas
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    where the thylacines were common.
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    I've even spoken to people, like Peter Carter here,
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    who when I spoke to him was 90 years old,
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    but in 1926, this man and his father and his brother
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    caught thylacines. They trapped them.
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    And it just, when I spoke to this man,
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    I was looking in his eyes and thinking,
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    behind those eyes is a brain
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    that has memories of what thylacines feel like,
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    what they smelled like, what they sounded like.
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    He led them around on a rope.
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    He has personal experiences
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    that I would give my left leg to have in my head.
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    We'd all love to have this sort of thing happen.
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    Anyway, I asked Peter, by any chance,
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    could he take us back to where he caught those thylacines.
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    My interest was in whether the environment had changed.
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    He thought hard. I mean, it was nearly 80 years before this
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    that he'd been at this hut.
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    At any rate, he led us down this bush track,
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    and there, right where he remembered, was the hut,
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    and tears came into his eyes.
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    He looked at the hut. We went inside.
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    There were the wooden boards on the sides of the hut
  • 15:09 - 15:12
    where he and his father and his brother had slept at night.
  • 15:12 - 15:15
    And he told me, as it all was flooding back in memories.
  • 15:15 - 15:18
    He said, "I remember the thylacines going around the hut
  • 15:18 - 15:20
    wondering what was inside," and he said
  • 15:20 - 15:23
    they made sounds like "Yip! Yip! Yip!"
  • 15:23 - 15:26
    All of these are parts of his life and what he remembers.
  • 15:26 - 15:29
    And the key question for me was to ask Peter,
  • 15:29 - 15:31
    has it changed? And he said no.
  • 15:31 - 15:33
    The southern beech forests surrounded his hut
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    just like it was when he was there in 1926.
  • 15:36 - 15:38
    The grasslands were sweeping away.
  • 15:38 - 15:40
    That's classic thylacine habitat.
  • 15:40 - 15:42
    And the animals in those areas were the same
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    that were there when the thylacine was around.
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    So could we put it back? Yes.
  • 15:47 - 15:50
    Is that all we would do? And this is an interesting question.
  • 15:50 - 15:53
    Sometimes you might be able to put it back,
  • 15:53 - 15:54
    but is that the safest way to make sure
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    it never goes extinct again, and I don't think so.
  • 15:57 - 16:00
    I think gradually, as we see species all around the world,
  • 16:00 - 16:03
    it's kind of a mantra that wildlife is increasingly
  • 16:03 - 16:05
    not safe in the wild.
  • 16:05 - 16:07
    We'd love to think it is, but we know it isn't.
  • 16:07 - 16:09
    We need other parallel strategies coming online.
  • 16:09 - 16:11
    And this one interests me.
  • 16:11 - 16:13
    Some of the thylacines that were being turned into zoos,
  • 16:13 - 16:15
    sanctuaries, even at the museums,
  • 16:15 - 16:17
    had collar marks on the neck.
  • 16:17 - 16:19
    They were being kept as pets,
  • 16:19 - 16:22
    and we know a lot of bush tales and memories
  • 16:22 - 16:24
    of people who had them as pets,
  • 16:24 - 16:26
    and they say they were wonderful, friendly.
  • 16:26 - 16:29
    This particular one came in out of the forest
  • 16:29 - 16:32
    to lick this boy and curled up
  • 16:32 - 16:34
    around the fireplace to go to sleep. A wild animal.
  • 16:34 - 16:37
    And I'd like to ask the question, all of --
  • 16:37 - 16:39
    we need to think about this.
  • 16:39 - 16:43
    If it had not been illegal to keep these thylacines as pets
  • 16:43 - 16:46
    then, would the thylacine be extinct now?
  • 16:46 - 16:48
    And I'm positive it wouldn't.
  • 16:48 - 16:51
    We need to think about this in today's world.
  • 16:51 - 16:54
    Could it be that getting animals close to us
  • 16:54 - 16:57
    so that we value them, maybe they won't go extinct?
  • 16:57 - 16:59
    And this is such a critical issue for us,
  • 16:59 - 17:02
    because if we don't do that, we're going to watch
  • 17:02 - 17:05
    more of these animals plunge off the precipice.
  • 17:05 - 17:07
    As far as I'm concerned, this is why
  • 17:07 - 17:10
    we're trying to do these kinds of de-extinction projects.
  • 17:10 - 17:14
    We are trying to restore that balance of nature
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    that we have upset.
  • 17:16 - 17:17
    Thank you.
  • 17:17 - 17:20
    (Applause)
Title:
How we'll resurrect the gastric brooding frog, the Tasmanian tiger
Speaker:
Michael Archer
Description:

The gastric brooding frog lays its eggs just like any other frog -- then swallows them whole to incubate. That is, it did until it went extinct 30 years ago. Paleontologist Michael Archer makes a case to bring back the gastric brooding frog and the thylacine, commonly known as the Tasmanian tiger. (Filmed at TEDxDeExtinction.)

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Video Language:
English
Team:
closed TED
Project:
TEDTalks
Duration:
17:36

English subtitles

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