Can we resurrect the thylacine? Maybe, but it won’t help the global extinction crisis

9 03 2022

NFSA

(published first on The Conversation)

Last week, researchers at the University of Melbourne announced that thylacines or Tasmanian tigers, the Australian marsupial predators extinct since the 1930s, could one day be ushered back to life.

The thylacine (Thylacinus cynocephalus), also known as the ‘Tasmanian tiger’ (it was neither Tasmanian, because it was once common in mainland Australia, nor was it related to the tiger), went extinct in Tasmania in the 1930s from persecution by farmers and habitat loss. Art by Eleanor (Nellie) Pease, University of Queensland.
Centre of Excellence for Australian Biodiversity and Heritage

The main reason for the optimism was the receipt of a A$5 million philanthropic donation to the research team behind the endeavour.

Advances in mapping the genome of the thylacine and its living relative the numbat have made the prospect of re-animating the species seem real. As an ecologist, I would personally relish the opportunity to see a living specimen.

The announcement led to some overhyped headlines about the imminent resurrection of the species. But the idea of “de-extinction” faces a variety of technical, ethical and ecological challenges. Critics (like myself) argue it diverts attention and resources from the urgent and achievable task of preventing still-living species from becoming extinct.

The rebirth of the bucardo

The idea of de-extinction goes back at least to the the creation of the San Diego Frozen Zoo in the early 1970s. This project aimed to freeze blood, DNA, tissue, cells, eggs and sperm from exotic and endangered species in the hope of one day recreating them.

The notion gained broad public attention with the first of the Jurassic Park films in 1993. The famous cloning of Dolly the sheep reported in 1996 created a sense that the necessary know-how wasn’t too far off.

The next technological leap came in 2008, with the cloning of a dead mouse that had been frozen at –20℃ for 16 years. If frozen individuals could be cloned, re-animation of a whole species seemed possible.

After this achievement, de-extinction began to look like a potential way to tackle the modern global extinction crisis.

Read the rest of this entry »




Why populations can’t be saved by a single breeding pair

3 04 2018

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© Reuters/Thomas Mukoya

I published this last week on The Conversation, and now reproducing it here for CB.com readers.

 

Two days ago, the last male northern white rhino (Ceratotherium simum cottoni) died. His passing leaves two surviving members of his subspecies: both females who are unable to bear calves.

Even though it might not be quite the end of the northern white rhino because of the possibility of implanting frozen embryos in their southern cousins (C. simum simum), in practical terms, it nevertheless represents the end of a long decline for the subspecies. It also raises the question: how many individuals does a species need to persist?

Fiction writers have enthusiastically embraced this question, most often in the post-apocalypse genre. It’s a notion with a long past; the Adam and Eve myth is of course based on a single breeding pair populating the entire world, as is the case described in the Ragnarok, the final battle of the gods in Norse mythology.

This idea dovetails neatly with the image of Noah’s animals marching “two by two” into the Ark. But the science of “minimum viable populations” tells us a different story.

No inbreeding, please

The global gold standard used to assess the extinction risk of any species is the International Union for the Conservation of Nature (IUCN) Red List of Threatened Species. Read the rest of this entry »





Genetic Management of Fragmented Animal and Plant Populations

10 12 2016

logoThat is the title of a new textbook that will be available mid-2017.

After almost 6 years work, authors Dick Frankham, Jonathan Ballou, Katherine Ralls, Mark Eldridge, Michele Dudash, Charles Fenster, Bob Lacy & Paul Sunnucks have produced an advanced textbook/research monograph that aims to provoke a paradigm shift in the management of small, isolated population fragments of animals and plants.

One of the greatest unmet challenges in conservation biology is the genetic management of fragmented populations of threatened animal and plant species. More than a million small, isolated, population fragments of threatened species are likely suffering inbreeding depression, loss of evolutionary potential, and elevated extinction risks (genetic erosion). Re-establishing gene flow between populations is required to reverse these effects, but managers very rarely do this. On the contrary, molecular genetic methods are mainly being used to document genetic differentiation among populations, with most studies concluding that genetically differentiated populations should be managed separately (i.e., kept isolated), thereby dooming many populations to eventual extinction.

The need for a paradigm shift in genetic management of fragmented populations has been highlighted as a major issue in conservation. The rapidly advancing field of molecular genetics is continually providing new tools to measure the extent of population fragmentation and its genetic consequences. However, adequate guidance on how to use these data for effective conservation is still lacking, and many populations are going extinct principally for genetic reasons. Consequently, there is now urgent need for an authoritative textbook on the subject.

Read the rest of this entry »





Extinction synergy: deadly combination of human hunting & climate change wrote off Patagonian giants

20 06 2016

MegatheriumHere’s a paper we’ve just had published in Science Advances (Synergistic roles of climate warming and human occupation in Patagonian megafaunal extinctions during the Last Deglaciation). It’s an excellent demonstration of our concept of extinction synergies that we published back in 2008.

Giant Ice Age species including elephant-sized sloths and powerful sabre-toothed cats that once roamed the windswept plains of Patagonia, southern South America, were finally felled by a perfect storm of a rapidly warming climate and humans, a new study has shown.

Research published on Saturday in Science Advances, has revealed that it was only when the climate warmed, long after humans first arrived in Patagonia, did the megafauna suddenly die off around 12,300 years ago.

The timing and cause of rapid extinctions of the megafauna has remained a mystery for centuries.

“Patagonia turns out to be the Rosetta Stone – it shows that human colonisation didn’t immediately result in extinctions, but only as long as it stayed cold”. “Instead, more than 1000 years of human occupation passed before a rapid warming event occurred, and then the megafauna were extinct within a hundred years.”

The researchers, including from the University of Colorado Boulder, University of New South Wales and University of Magallanes in Patagonia, studied ancient DNA extracted from radiocarbon-dated bones and teeth found in caves across Patagonia, and Tierra del Fuego, to trace the genetic history of the populations. Species such as the South American horse, giant jaguar and sabre-toothed cat, and the enormous one-tonne short-faced bear (the largest land-based mammalian carnivore) were found widely across Patagonia, but seemed to disappear shortly after humans arrived. Read the rest of this entry »





Ice Age? No. Abrupt warmings and hunting together polished off Holarctic megafauna

24 07 2015

Oh shit oh shit oh shit ...

Oh shit oh shit oh shit …

Did ice ages cause the Pleistocene megafauna to go extinct? Contrary to popular opinion, no, they didn’t. But climate change did have something to do with them, only it was global warming events instead.

Just out today in Science, our long-time-coming (9 years in total if you count the time from the original idea to today) paper ‘Abrupt warmings drove Late Pleistocene Holarctic megafaunal turnover‘ demonstrates for the first time that abrupt warming periods over the last 60,000 years were at least partially responsible for the collapse of the megafauna in Eurasia and North America.

You might recall that I’ve been a bit sceptical of claims that climate changes had much to do with megafauna extinctions during the Late Pleistocene and early Holocene, mainly because of the overwhelming evidence that humans had a big part to play in their demise (surprise, surprise). What I’ve rejected though isn’t so much that climate had nothing to do with the extinctions; rather, I took issue with claims that climate change was the dominant driver. I’ve also had problems with blanket claims that it was ‘always this’ or ‘always that’, when the complexity of biogeography and community dynamics means that it was most assuredly more complicated than most people think.

I’m happy to say that our latest paper indeed demonstrates the complexity of megafauna extinctions, and that it took a heap of fairly complex datasets and analyses to demonstrate. Not only were the data varied – the combination of scientists involved was just as eclectic, with ancient DNA specialists, palaeo-climatologists and ecological modellers (including yours truly) assembled to make sense of the complicated story that the data ultimately revealed. Read the rest of this entry »





Avoiding genetic rescue not justified on genetic grounds

12 03 2015

Genetics to the rescue!

Genetics to the rescue!

I had the pleasure today of reading a new paper by one of the greatest living conservation geneticists, Dick Frankham. As some of CB readers might remember, I’ve also published some papers with Dick over the last few years, with the most recent challenging the very basis for the IUCN Red List category thresholds (i.e., in general, they’re too small).

Dick’s latest paper in Molecular Ecology is a meta-analysis designed to test whether there are any genetic grounds for NOT attempting genetic rescue for inbreeding-depressed populations. I suppose a few definitions are in order here. Genetic rescue is the process, either natural or facilitated, where inbred populations (i.e., in a conservation sense, those comprising too many individuals bonking their close relatives because the population in question is small) receive genes from another population such that their overall genetic diversity increases. In the context of conservation genetics, ‘inbreeding depression‘ simply means reduced biological fitness (fertility, survival, longevity, etc.) resulting from parents being too closely related.

Seems like an important thing to avoid, so why not attempt to facilitate gene flow among populations such that those with inbreeding depression can be ‘rescued’? In applied conservation, there are many reasons given for not attempting genetic rescue: Read the rest of this entry »





We’re sorry, but 50/500 is still too few

28 01 2014

too fewSome of you who are familiar with my colleagues’ and my work will know that we have been investigating the minimum viable population size concept for years (see references at the end of this post). Little did I know when I started this line of scientific inquiry that it would end up creating more than a few adversaries.

It might be a philosophical perspective that people adopt when refusing to believe that there is any such thing as a ‘minimum’ number of individuals in a population required to guarantee a high (i.e., almost assured) probability of persistence. I’m not sure. For whatever reason though, there have been some fierce opponents to the concept, or any application of it.

Yet a sizeable chunk of quantitative conservation ecology develops – in various forms – population viability analyses to estimate the probability that a population (or entire species) will go extinct. When the probability is unacceptably high, then various management approaches can be employed (and modelled) to improve the population’s fate. The flip side of such an analysis is, of course, seeing at what population size the probability of extinction becomes negligible.

‘Negligible’ is a subjective term in itself, just like the word ‘very‘ can mean different things to different people. This is why we looked into standardising the criteria for ‘negligible’ for minimum viable population sizes, almost exactly what the near universally accepted IUCN Red List attempts to do with its various (categorical) extinction risk categories.

But most reasonable people are likely to agree that < 1 % chance of going extinct over many generations (40, in the case of our suggestion) is an acceptable target. I’d feel pretty safe personally if my own family’s probability of surviving was > 99 % over the next 40 generations.

Some people, however, baulk at the notion of making generalisations in ecology (funny – I was always under the impression that was exactly what we were supposed to be doing as scientists – finding how things worked in most situations, such that the mechanisms become clearer and clearer – call me a dreamer).

So when we were attacked in several high-profile journals, it came as something of a surprise. The latest lashing came in the form of a Trends in Ecology and Evolution article. We wrote a (necessarily short) response to that article, identifying its inaccuracies and contradictions, but we were unable to expand completely on the inadequacies of that article. However, I’m happy to say that now we have, and we have expanded our commentary on that paper into a broader review. Read the rest of this entry »





Cleaning up the rubbish: Australian megafauna extinctions

15 11 2013

diprotodonA few weeks ago I wrote a post about how to run the perfect scientific workshop, which most of you thought was a good set of tips (bizarrely, one person was quite upset with the message; I saved him the embarrassment of looking stupid online and refrained from publishing his comment).

As I mentioned at the end of post, the stimulus for the topic was a particularly wonderful workshop 12 of us attended at beautiful Linnaeus Estate on the northern coast of New South Wales (see Point 5 in the ‘workshop tips’ post).

But why did a group of ecological modellers (me, Barry Brook, Salvador Herrando-Pérez, Fréd Saltré, Chris Johnson, Nick Beeton), geneticists, palaeontologists (Gav Prideaux), fossil dating specialists (Dizzy Gillespie, Bert Roberts, Zenobia Jacobs) and palaeo-climatologists (Michael Bird, Chris Turney [in absentia]) get together in the first place? Hint: it wasn’t just the for the beautiful beach and good wine.

I hate to say it – mainly because it deserves as little attention as possible – but the main reason is that we needed to clean up a bit of rubbish. The rubbish in question being the latest bit of excrescence growing on that accumulating heap produced by a certain team of palaeontologists promulgating their ‘it’s all about the climate or nothing’ broken record.

Read the rest of this entry »





Does conservation biology need DNA barcoding?

5 01 2012

In November last year I was invited to participate in a panel discussion onthe role of DNA barcoding in conservation science. The discussion took place during the 4th International Barcode of Life Conference (which I didn’t actually attend) in Adelaide, and was hosted by that media-tart-and-now-director-of-the-Royal-Institution, Dr. Paul Willis.

Paul has recently blogged about the ‘species’ concept as it relates to DNA barcoding, which I highly recommend. It also prompted me to write this post because now the video of the discussion is available online (see below).

Now, the panel was a bit of a funny set-up in a way – I was really one of the only ‘conservation biologists’ represented (Patrick O’Connor and Andy Lowe perhaps excepted), with the rest mainly made up of molecular people (Pete Hollingsworth, Bob Hanner, Karen James) – and I was told prior to the ‘debate’ that I was meant to be the contrarian (i.e., that there is no role for DNA barcoding in conservation).

Fundamentally, I don’t actually embrace the contrarian view on this one given that I see no reason why DNA barcoding can’t enhance or refine our conservation knowledge and skills. But the ‘debate’ did raise some important issues about technological advancements in the application of conservation science to real conservation.

I suppose that prior to getting stuck into the polemic I should define DNA barcoding for the uninitiated; it’s a basic technique that analyses short sequences of DNA with the sole purposes of identifying from which species they come. Imagine walking through the bush with a barcode scanner and pointing at random species you see and getting an instant identification read-out without actually knowing the species beforehand. You can see why it’s called ‘barcoding’ because it is like running products through the check-out to get instant price details. Read the rest of this entry »








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