Population of First Australians grew to millions, much more than previous estimates

30 04 2021

Shutterstock/Jason Benz Bennee


We know it is more than 60,000 years since the first people entered the continent of Sahul — the giant landmass that connected New Guinea, Australia and Tasmania when sea levels were lower than today.

But where the earliest people moved across the landscape, how fast they moved, and how many were involved, have been shrouded in mystery.

Our latest research, published today shows the establishment of populations in every part of this giant continent could have occurred in as little as 5,000 years. And the entire population of Sahul could have been as high as 6.4 million people.

This translates to more than 3 million people in the area that is now modern-day Australia, far more than any previous estimate.


Read more: We mapped the ‘super-highways’ the First Australians used to cross the ancient land


The first people could have entered through what is now western New Guinea or from the now-submerged Sahul Shelf off the modern-day Kimberley (or both).

But whichever the route, entire communities of people arrived, adapted to and established deep cultural connections with Country over 11 million square kilometres of land, from northwestern Sahul to Tasmania.

A map showing a much larger landmass as Australia is joined to both Tasmania and New Guinea due to lower sea levels

Map of what Australia looked like for most of the human history of the continent when sea levels were lower than today. Author provided


This equals a rate of population establishment of about 1km per year (based on a maximum straight-line distance of about 5,000km from the introduction point to the farthest point).

That’s doubly impressive when you consider the harshness of the Australian landscape in which people both survived and thrived.

Previous estimates of Indigenous population

Various attempts have been made to calculate the number of people living in Australia before European invasion. Estimates vary from 300,000 to more than 1,200,000 people. Read the rest of this entry »





The biggest and slowest don’t always bite it first

13 04 2021

For many years I’ve been interested in modelling the extinction dynamics of megafauna. Apart from co-authoring a few demographically simplified (or largely demographically free) models about how megafauna species could have gone extinct, I have never really tried to capture the full nuances of long-extinct species within a fully structured demographic framework.

That is, until now.

But how do you get the life-history data of an extinct animal that was never directly measured. Surely, things like survival, reproductive output, longevity and even environmental carrying capacity are impossible to discern, and aren’t these necessary for a stage-structured demographic model?

Thylacine mum & joey. Nellie Pease & CABAH

The answer to the first part of that question “it’s possible”, and to the second, it’s “yes”. The most important bit of information we palaeo modellers need to construct something that’s ecologically plausible for an extinct species is an estimate of body mass. Thankfully, palaeontologists are very good at estimating the mass of the things they dig up (with the associated caveats, of course). From such estimates, we can reconstruct everything from equilibrium densities, maximum rate of population growth, age at first breeding, and longevity.

But it’s more complicated than that, of course. In Australia anyway, we’re largely dealing with marsupials (and some monotremes), and they have a rather different life-history mode than most placentals. We therefore have to ‘correct’ the life-history estimates derived from living placental species. Thankfully, evolutionary biologists and ecologists have ways to do that too.

The Pleistocene kangaroo Procoptodon goliah, the largest and most heavily built of the  short-faced kangaroos, was the largest and most heavily built kangaroo known. It had an  unusually short, flat face and forwardly directed 
eyes, with a single large toe on each foot  (reduced from the more normal count of four). Each forelimb had two long, clawed fingers  that would have been used to bring leafy branches within reach.

So with a battery of ecological, demographic, and evolutionary tools, we can now create reasonable stochastic-demographic models for long-gone species, like wombat-like creatures as big as cars, birds more than two metres tall, and lizards more than seven metres long that once roamed the Australian continent. 

Ancient clues, in the shape of fossils and archaeological evidence of varying quality scattered across Australia, have formed the basis of several hypotheses about the fate of megafauna that vanished during a peak about 42,000 years ago from the ancient continent of Sahul, comprising mainland Australia, Tasmania, New Guinea and neighbouring islands.

There is a growing consensus that multiple factors were at play, including climate change, the impact of people on the environment, and access to freshwater sources.

Just published in the open-access journal eLife, our latest CABAH paper applies these approaches to assess how susceptible different species were to extinction – and what it means for the survival of species today. 

Using various characteristics such as body size, weight, lifespan, survival rate, and fertility, we (Chris Johnson, John Llewelyn, Vera Weisbecker, Giovanni Strona, Frédérik Saltré & me) created population simulation models to predict the likelihood of these species surviving under different types of environmental disturbance.

Simulations included everything from increasing droughts to increasing hunting pressure to see which species of 13 extinct megafauna (genera: Diprotodon, Palorchestes, Zygomaturus, Phascolonus, Procoptodon, Sthenurus, Protemnodon, Simosthenurus, Metasthenurus, Genyornis, Thylacoleo, Thylacinus, Megalibgwilia), as well as 8 comparative species still alive today (Vombatus, Osphranter, Notamacropus, Dromaius, Alectura, Sarcophilus, Dasyurus, Tachyglossus), had the highest chances of surviving.

We compared the results to what we know about the timing of extinction for different megafauna species derived from dated fossil records. We expected to confirm that the most extinction-prone species were the first species to go extinct – but that wasn’t necessarily the case.

While we did find that slower-growing species with lower fertility, like the rhino-sized wombat relative Diprotodon, were generally more susceptible to extinction than more-fecund species like the marsupial ‘tiger’ thylacine, the relative susceptibility rank across species did not match the timing of their extinctions recorded in the fossil record.

Indeed, we found no clear relationship between a species’ inherent vulnerability to extinction — such as being slower and heavier and/or slower to reproduce — and the timing of its extinction in the fossil record.

In fact, we found that most of the living species used for comparison — such as short-beaked echidnas, emus, brush turkeys, and common wombats — were more susceptible on average than their now-extinct counterparts.

Read the rest of this entry »




How to avoid reduce the probability of being killed by a shark

31 03 2021

Easy. Don’t go swimming/surfing/snorkelling/diving in the ocean.


“Oh, shit”

Sure, that’s true, but if you’re like many Australians, the sea is not just a beautiful thing to look at from the window, it’s a way of life. Trying telling a surfer not to surf, or a diver not to dive. Good luck with that.

A few years ago, I joined a team of super-cool sharkologists led by Charlie ‘Aussie-by-way-of-Belgium shark-scientist extraordinaire Huveneers, and including Maddie ‘Chomp’ Thiele and Lauren ‘Acid’ Meyer — to publish the results of some of the first experimentally tested shark deterrents.

It turns out that many of the deterrents we tested failed to show any reduction in the probability of a shark biting, with only one type of electronic deterrent showing any effect at all (~ 60% reduction).

Great. But what might that mean in terms of how many people could be saved by wearing such electronic deterrents? While the probability of being bitten by a shark is low globally, even in Australia (despite public perceptions), we wondered if the number of lives saved and injuries avoided was substantial.

In a new paper just published today in Royal Society Open Science, we attempted to answer that question.

To predict how many people could avoid shark bites if they were using properly donned electronic deterrents that demonstrate some capacity to dissuade sharks from biting, we examined the century-scale time series of shark bites on humans in Australia. This database — the ‘Australian Shark Attack File‘ — is one of the most comprehensive databases of its kind.

Read the rest of this entry »




Conservation paradox – the pros and cons of recreational hunting

20 02 2021
The recovery of species such as mountain zebra (Equus zebra) was partly supported by the economic benefits generated by trophy hunting. © Dr Hayley Clements

Through the leadership of my long-time friend and collaborator, Enrico Di Minin of the Helsinki Lab of Interdisciplinary Conservation Science, as well as the co-leadership of my (now) new colleague, Dr Hayley Clements, I’m pleased to report our new paper in One Earth — ‘Consequences of recreational hunting for biodiversity conservation and livelihoods‘.


My father was a hunter, and by proxy so was I when I was a lad. I wasn’t really a ‘good’ hunter in the sense that I rarely bagged my quarry, but during my childhood not only did I fail to question the morality of recreational hunting, I really thought that in fact it was by and large an important cultural endeavour.

It’s interesting how conditioned we become as children, for I couldn’t possibly conceive of hunting a wild, indigenous species for my own personal satisfaction now. I find the process not only morally and ethically reprehensible, I also think that most species don’t need the extra stress in an already environmentally stressed world.

I admit that I do shoot invasive European rabbits and foxes on my small farm from time to time — to reduce the grazing and browsing pressure on my trees from the former, and the predation pressure on the chooks from the latter. Of course, we eat the rabbits, but I tend just to bury the foxes. My dual perspective on the general issue of hunting in a way mirrors the two sides of the recreational hunting issue we report in our latest paper.

Wild boar (Sus scrofus). Photo: Valentin Panzirsch, CC BY-SA 3.0 AT, via Wikimedia Commons

I want to be clear here that our paper focuses exclusively on recreational hunting, and especially the hunting of charismatic species for their trophies. The activity is more than just a little controversial, for it raises many ethical and moral concerns at the very least. Yet, recreational hunting is frequently suggested as a way to conserve nature and support local people’s livelihoods. 

Read the rest of this entry »




Job: Research Associate in Mammalian Morphology-Environment Interactions

15 02 2021

This might be a little outside the realms of ‘conservation’ per se, but put has a lot of ecology-evolution components, with spin-off applications to modern conservation. Please spread the word.



The Research Associate will investigate how the skull of extant mammal populations varies according to their environment, with a focus on the interaction between mega-herbivores and vegetation change.

The project aims to understand the relationship between evolved morphological adaptation and phenotypic plasticity in changing local environments. The Research Associate will extrapolate this knowledge to the iconic extinct Australian megafauna, with the aim of establishing how changing conditions of the past might have contributed to the demise of the Australian megafauna.

The candidate will be expected to work within a large group of collaborators at Flinders University and interstate, and supervise postgraduate students. The collaboration environment includes teams of national and international researchers, and will particularly integrate research in Global Ecology Lab led by Corey Bradshaw, and Chris Johnson‘s lab at the University of Tasmania. The candidate will be expected to liaise with academic, administrative and technical staff according to the University’s policies, practices and standards.

Key position responsibilities

The Research Associate will be responsible for:

Read the rest of this entry »




Plan B: COVID-19 challenges for field-based PhD students

8 12 2020

Originally published on the GEL.blog


Blistering heat, pouring rain, finding volunteers, submitting field-trip forms, forgetting equipment, data sheets blowing away in the wind — a field-based research project is hard at the best of times. Add white sharks into the mix and you start to question whether this project is even possible. These were some of my realisations when I started my Honours year studying shark deterrents. 

A specific memory from my first field expedition was setting off on a six-day boat trip with the comfortable sight of land getting smaller and smaller, in an already rough ocean, to find one of the most feared fish in the sea, the white shark. I was intimidated, but also excited. 

Over the next few days reality set in and I experienced the true challenges of working in the field. When there were no sharks around, I had to concentrate on the bait line for hours in anticipation of a sudden ambush. When there were sharks around, it was all systems go and there was no room for error — not with a fish of this size. It didn’t matter how tired or seasick I was, the data had to be collected. 

When I found out that I had been offered a field-based PhD extending my shark-deterrent research from my Honours, other than being over-the-moon, I knew I had a big few years ahead of me. I immediately began preparing mentally for the challenges that came along with my field-based research. Particularly the long periods of time I knew I would spend away from home and my family. 

Read the rest of this entry »




Grand Challenges in Global Biodiversity Threats

8 10 2020

Last week I mentioned that the new journal Frontiers in Conservation Science is now open for business. As promised, I wrote a short article outlining our vision for the Global Biodiversity Threats section of the journal. It’s open-access, of course, so I’m also copying here on ConservationBytes.com.


Most conservation research and its applications tend to happen most frequently at reasonably fine spatial and temporal scales — for example, mesocosm experiments, single-species population viability analyses, recovery plans, patch-level restoration approaches, site-specific biodiversity surveys, et cetera. Yet, at the other end of the scale spectrum, there have been many overviews of biodiversity loss and degradation, accompanied by the development of multinational policy recommendations to encourage more sustainable decision making at lower levels of sovereign governance (e.g., national, subnational).

Yet truly global research in conservation science is fact comparatively rare, as poignantly demonstrated by the debates surrounding the evidence for and measurement of planetary tipping points (Barnosky et al., 2012; Brook et al., 2013; Lenton, 2013). Apart from the planetary scale of human-driven disruption to Earth’s climate system (Lenton, 2011), both scientific evidence and policy levers tend to be applied most often at finer, more tractable research and administrative scales. But as the massive ecological footprint of humanity has grown exponentially over the last century (footprintnetwork.org), robust, truly global-scale evidence of our damage to the biosphere is now starting to emerge (Díaz et al., 2019). Consequently, our responses to these planet-wide phenomena must also become more global in scope.

Conservation scientists are adept at chronicling patterns and trends — from the thousands of vertebrate surveys indicating an average reduction of 68% in the numbers of individuals in populations since the 1970s (WWF, 2020), to global estimates of modern extinction rates (Ceballos and Ehrlich, 2002; Pimm et al., 2014; Ceballos et al., 2015; Ceballos et al., 2017), future models of co-extinction cascades (Strona and Bradshaw, 2018), the negative consequences of invasive species across the planet (Simberloff et al., 2013; Diagne et al., 2020), discussions surrounding the evidence for the collapse of insect populations (Goulson, 2019; Komonen et al., 2019; Sánchez-Bayo and Wyckhuys, 2019; Cardoso et al., 2020; Crossley et al., 2020), the threats to soil biodiversity (Orgiazzi et al., 2016), and the ubiquity of plastic pollution (Beaumont et al., 2019) and other toxic substances (Cribb, 2014), to name only some of the major themes in global conservation. 

Read the rest of this entry »




New journal: Frontiers in Conservation Science

29 09 2020

Several months ago, Daniel Blumstein of UCLA approached me with an offer — fancy leading a Special Section in a new Frontiers journal dedicated to conservation science?

I admit that my gut reaction was a visceral ‘no’, both in terms of the extra time it would require, as well as my autonomous reflex of ‘not another journal, please‘.

I had, for example, spent a good deal of blood, sweat, and tears helping to launch Conservation Letters when I acted as Senior Editor for the first 3.5 years of its existence (I can’t believe that it has been nearly a decade since I left the journal). While certainly an educational and reputational boost, I can’t claim that the experience was always a pleasant one — as has been said many times before, the fastest way to make enemies is to become an editor.

But then Dan explained what he had in mind for Frontiers in Conservation Science, and the more I spoke with him, the more I started to think that it wasn’t a bad idea after all for me to join.

Read the rest of this entry »





Many animals won’t cope with climate change without access to ample drinking water

12 08 2020

Climate change implies change in temperature and water, and both factors shape species’ tolerances to thermal stress. In our latest article, we show that lack of drinking water maximises differences in tolerance to high temperatures among populations of Iberian lizard species.

drinking

Climate change is a multidimensional phenomenon comprising temporal and spatial shifts in both temperature and precipitation (1). How we perceive climate change depends on whether we measure it as shift in (i) mean conditions (e.g., the mean air temperature or rainfall over a decade within a given territory), (ii) magnitude or frequency of extreme conditions (e.g., the frequency of floods or tornados or the number of days with temperatures or rainfall above or below a given threshold), or (iii) speed at which mean or extreme conditions change in space and/or time.

In aquatic ecosystems, climate change further alters water acidity, oxygen dissolution and melting of ice. However, many people, including some scientists, tend to equate climate change erroneously with increased mean temperatures. Psychologists have made the semantic point that the use of the expressions climate change and global warming as synonyms can give mixed messages to politicians, and society in general, about how serious and complex the climate emergency we are facing really is (2, 3) — see NASA’s simple-worded account on the subject here.

In our latest article (4), we reviewed the ecological literature to determine to what extent ecologists investigating the tolerance of terrestrial animals to high temperatures have looked at thermal effects over water effects. It turns out, they were five times more likely to examine temperature over water.

cb_BAAE_WaterLizardsNetwork

Frequency of correlations between climate (air temperature versus precipitation) and tolerance to high temperature of terrestrial fauna in 64 papers published in the ecological literature (thickest link = 36, thinnest link = 2) following a systematic literature review in Scopus (4).

This is counterintuitive. Just imagine you have been walking under the sun for several hours on one of those dog days of summer, and you are offered to choose between a sunshade or a bottle of water. I’d bet you’d choose the bottle of water.

Read the rest of this entry »





History of species distribution models

21 07 2020

This little historical overview by recently completed undergraduate student, Sofie Costin (soon to join our lab!), nicely summarises the history, strengths, and limitations of species distribution modelling in ecology, conservation and restoration. I thought it would be an excellent resource for those who are just entering the world of species distribution models.

SDM

Of course, there is a strong association between and given species and its environment1. As such, climate and geographical factors have been often used to explain the distribution of plant and animal species around the world.

Predictive ecological models, otherwise known as ‘niche models’ or ‘species distribution models’ have become a widely used tool for the planning of conservation strategies such as pest management and translocations2-5. In short, species distribution models assess the relationship between environmental conditions and species’ occurrences, and then can estimate the spatial distribution of habitats suited to the study species outside of the sampling area3,6.

While the application of species distribution models can reduce the time and cost associated with conservation research, and conservation managers are relying increasingly on them to inform their conservation strategies4, species distribution models are by no means a one-stop solution to all conservation issues. Read the rest of this entry »





I’m nearing the end of my PhD/postdoc … What the hell am I supposed to do now?

13 07 2020

Originally published on the GE.blog.

What do you want to be when you grow up?

Elasmotherium

Unicorns, like job security, used to exist (actually, it’s an Elasmotherium)

The term ‘job security’ seems a fanciful idea to budding biologists — you may as well be studying unicorns (and no, narwhal don’t count …)! Now, you’re a fully fledged adult, your thoughts are likely filled with adult questions like ‘where will I live’ and ‘how will I scrape some money together?’. Not knowing where to go next can be very stressful.

A change in profession might help with job security, but if you’ve made it this far in biology, its highly likely that you (like me) have been obsessed with biology since early childhood, and it’s not something you’re willing to give up easily. On top of that, you now have years of research experience and skill development behind you — it would be better if that experience didn’t go to waste. How, then, can we keep funding our biology addiction? I don’t want to sound like a snake-oil salesman here, so let’s be straight-up about this: there are no easy options. But, importantly, there are options — in research, the university sector, and wider afield.

So, down to the serious business. Your options (depending on your personal preferences) are:

1. Research or bust!

In-house postdoctoral fellowships

Research bodies in Australia, including many universities, the CSIRO and the Australian Museum, offer in-house postdoctoral fellowships for early-career researchers. Applying for one of these postdocs usually involves the candidate developing a research proposal and initiating collaboration with researchers in the institute offering the fellowship. Read the rest of this entry »





Journal ranks 2019

8 07 2020

journalstack_16x9

For the last 12 years and running, I’ve been generating journal ranks based on the journal-ranking method we published several years ago. Since the Google journal h-indices were just released, here are the new 2019 ranks for: (i) 99 ecology, conservation and multidisciplinary journals, and a subset of (ii) 61 ‘ecology’ journals, (iii) 27 ‘conservation’ journals, (iv) 41 ‘sustainability’ journals (with general and energy-focussed journals included), and (v) 20 ‘marine & freshwater’ journals.

See also the previous years’ rankings (2018, 20172016201520142013, 2012, 20112010, 2009, 2008).

Read the rest of this entry »





Successful movers responding to climate change

16 06 2020

tropical fishes range shiftsEcologists often rely on measuring certain elements of a species’ characteristics, behaviour, or morphology to determine if these — what we call ‘traits’ — give them certain capacities to exploit their natural environments. While sometimes a bit arbitrarily defined, the traits that can be measured are many indeed, and sometimes they reveal rather interesting elements of a species’ resilience in the face of environmental change.

As we know, climate change is changing the way species are distributed around the planet, for the main (and highly simplified) reason that the environments in which they’ve evolved and to which they have adapted are changing.

In the simplest case, a warming climate means that there is a higher and higher chance you’ll experience temperatures that really don’t suit you that well (think of a koala or a flying fox baking in a tree when the thermometer reads +45° in the shade). Just like you seeking those nice, air-conditioned spaces on a scorcher of a day, species like to move to where conditions are more acceptable to their particular physiologies and behaviours.

When they can’t change fast enough, they go extinct.

Ecologists use life-history traits to predict which species have the highest probability of moving to new areas in response to climate change. Most studies into this phenomenon have largely ignored that range shifts in fact occur in sequential stages: (1) the species arrives in a new place for the first time, (2) its population increases in size (and extent), and (3) it can continue to persist in the new spot. Read the rest of this entry »





A plant’s adaptive traits don’t follow climate conditions as you might expect

27 03 2020

mountain

Just a quick post today, my last one for March. Like probably most of you, I’ve been trying to pretend to be as normal as possible despite the COVID-19 surrealism all around me. But even COVID-19 has shifted my research to a small degree.

But I’m not going to talk about the global pandemic right now (I can almost hear the collective sigh of relief). Instead, I’m going to go back to topic and discuss a paper that I’ve just co-authored.

Last year I went to China’s Yunnan Province where I met some fantastic colleagues at the Xishuangbanna Tropical Botanical Garden who were doing some very cool stuff with the variation in plant functional traits across environmental gradients.

Well, those colleagues invited me to participate in one those research projects, and I’m happy to say that the result has just been published in Forests.

Measuring the functional traits of different alpine trees species in the Changbai Mountains of far north-eastern China (no, I didn’t get to go there), the research set out to test how these varied among species and elevation.

Of course, one expects that different trees use different combinations of traits to survive the rigours of mountain life (high variation in temperature, freezing, wind, etc.), but generally speaking, you might expect things like xylem vessel diameter and density to change more or less monotonically (i.e., changing in a consistent manner as elevation rises or falls). This is because trees should adapt their traits to the local conditions as best they can. Read the rest of this entry »





In pursuit of an ecological resilience in the Anthropocene

3 03 2020

Changing TidesAn excerpt from Alejandro Frid‘s new book, Changing Tides: An Ecologist’s Journey to Make Peace with the Anthropocene (published first in Sierra, with photos courtesy of New Society Publishers)

The birth of my daughter, in 2004, thrust upon me a dual task: to be scientifically realistic about all the difficult changes that are here to stay, while staying humanly optimistic about the better things that we still have.

By the time my daughter turned eleven, I had jettisoned my nos­talgia for the Earth I was born into in the mid-196os—a planet that, of course, was an ecological shadow of Earth 100 years before, which in turn was an ecological shadow of an earlier Earth. The pragmatist in me had embraced the Anthropocene, in which humans dominate all biophysical processes, and I ended up feeling genuinely good about some of the possible futures in which my daughter’s generation might grow old.

It was a choice to engage in a tough situation. An acknowledgement of rapid and uninvited change. A reaffirmed commitment to everything I have learned, and continue to learn, as an ecologist working with Indigenous people on marine conservation. Fundamental to this perspective is the notion of resilience: the ability of someone or something—a culture, an ecosystem, an economy, a person—to absorb shocks yet still maintain their essence.

But what is essence? Read the rest of this entry »





Influential conservation ecology papers of 2019

24 12 2019

Bradshaw-Waves breaking on rocks Macquarie Island
As I’ve done for the last six years, I am publishing a retrospective list of the ‘top’ 20 influential papers of 2019 as assessed by experts in F1000 Prime (in no particular order). See previous years’ lists here: 20182017, 20162015, 2014, and 2013.

Read the rest of this entry »





Adult disguises

2 12 2019

Skilled ornithologists can tell the age of a bird by the look of its feathers. But many species are advancing the moult of their first adult plumage in response to global warming, and the youngsters look more similar to the adults now than two centuries ago.

R Graphics Output

The clothes don’t make the (wo)man, but how we dress sends out a lot of information about our tastes, emotional state, or financial situation. In nature, where species have evolved to exploit all kinds of physical and chemical cues, visual communication determines a wealth of feeding and reproductive strategies (1).

Birds are familiar to all of us by the beauty and variety of their plumages (see extreme examples commented by David Attenborough here, here and here), which bird fans use to tell juveniles from males, males from females and breeders from migrants. In evolutionary time, birds have gradually moved away from tree-bark browns and tree-leaf greens and, due to functional requirements, modern feathers only span about one third of the colours these animals can perceive (2). They obtain yellows, oranges, and reds from carotenoid-containing food, dark colours from melanin pigment of own synthesis, and the so-called structural colours depend on how light reflects on the barbs of the feathers (2).

Plumage, across its entire range of designs, is a factor crucial to the life history of our feathery friends and, consequently, to evaluate how and how much anthropogenic climate change is impacting them (3).

Plumage and temperature

We know that mammals and birds are modifying their fur and feathers to optimise camouflage against landscapes with more or less snow (4), but less-known are the implications of climate change for feather moulting. Read the rest of this entry »





Climate change and humans together pushed Australia’s biggest beasts to extinction

25 11 2019

people-megafaunaOver the last 60,000 years, many of the world’s largest species disappeared forever. Some of the largest that we generally call ‘megafauna’ were first lost in Sahul — the super-continent formed by the connection of Australia and New Guinea during periods of low sea level. The causes of these extinctions have been heavily debated for decades within the scientific community.

Three potential drivers of these extinctions have been suggested. The first is climate change that assumes an increase in arid conditions that eventually became lethal to megafauna. The second proposed mechanism is that the early ancestors of Aboriginal people who either hunted megafauna species to extinction, or modified ecosystems to put the largest species at a disadvantage. The third and most nuanced proposed driver of extinction is the combination of the first two.

The primary scientific tools we scientists use to determine which of these proposed causes of extinction have the most support are dated fossil records from the extinct species themselves, as well as archaeological evidence from early Aboriginal people. Traditionally, the main way we use these data is to construct a timeline of when the last fossil of a species was preserved, and compare this to evidence indicating when people arrived. We can also reconstruct climate patterns back tens of thousands of years using models similar to the ones used today to predict future climates. Based on the comparison of all of these different timelines, we conclude that abrupt climate changes in the past were influential if they occurred at or immediately before a recorded extinction event. On the other hand, if megafauna extinctions occur immediately after humans are thought to have arrived, we attribute more weight to human arrival as a driver.

Read the rest of this entry »





What is a ‘mass extinction’ and are we in one now?

13 11 2019

(reproduced from The Conversation)

For more than 3.5 billion years, living organisms have thrived, multiplied and diversified to occupy every ecosystem on Earth. The flip side to this explosion of new species is that species extinctions have also always been part of the evolutionary life cycle.

But these two processes are not always in step. When the loss of species rapidly outpaces the formation of new species, this balance can be tipped enough to elicit what are known as “mass extinction” events.


Read more: Climate change is killing off Earth’s little creatures


A mass extinction is usually defined as a loss of about three quarters of all species in existence across the entire Earth over a “short” geological period of time. Given the vast amount of time since life first evolved on the planet, “short” is defined as anything less than 2.8 million years.

Since at least the Cambrian period that began around 540 million years ago when the diversity of life first exploded into a vast array of forms, only five extinction events have definitively met these mass-extinction criteria.

These so-called “Big Five” have become part of the scientific benchmark to determine whether human beings have today created the conditions for a sixth mass extinction.

An ammonite fossil found on the Jurassic Coast in Devon. The fossil record can help us estimate prehistoric extinction rates. Corey Bradshaw, Author provided

Read the rest of this entry »





Victoria, please don’t aerial-bait dingoes

10 10 2019

Here’s a submission to Victoria’s proposed renewal of special permission from the Commonwealth to poison dingoes:

dingo with bait

08 October 2019

Honourable Lily D’Ambrosio MP
Minister for Energy, Environment and Climate Change
Level 16, 8 Nicholson Street, East Melbourne, VIC 3002

lily.dambrosio@parliament.vic.gov.au

cc:

The Hon Jaclyn Symes, Minister for Agriculture, Victoria

(jaclyn.symes@parliament.vic.gov.au)

Dr Sally Box, Threatened Species Commissioner

(ThreatenedSpeciesCommissioner@environment.gov.au)

The Hon Sussan Ley MP, Minister for Environment, Australia

(Farrer@aph.gov.au)

RE: RENEWAL OF AERIAL BAITING EXEMPTION IN VICTORIA FOR WILD DOG CONTROL USING 1080

Dear Minister,

The undersigned welcome the opportunity to comment on the proposed renewal of special permission from the Commonwealth under Sections 18 and 18A of the Environment Protection and Biodiversity Conservation Act 1999 (Commonwealth) to undertake aerial 1080 baiting in six Victorian locations for the management of ‘wild dogs’. This raises serious concerns for two species listed as threatened and protected in Victoria: (1) dingoes and (2) spot-tailed quolls (Dasyurus maculatus).

First, we must clarify that the terminology ‘wild dog’ is not appropriate when discussing wild canids in Australia. One of the main discussion points at the recent Royal Zoological Society of NSW symposium ‘Dingo Dilemma: Cull, Contain or Conserve’ was that the continued use of the terminology ‘wild dog’ is not justified because wild canids in Australia are predominantly dingoes and dingo hybrids, and not, in fact, feral domestic dogs. In Victoria, Stephens et al. (2015) observed that only 5 out of 623 wild canids (0.008%) sampled were feral domestic dogs with no evidence of dingo ancestry. This same study determined that 17.2% of wild canids in Victoria were pure or likely pure dingoes and 64.4% were hybrids with greater than 60% dingo ancestry. Additionally, comparative studies by Jones (1988, 1990 and 2009) observed that dingoes maintained a strong phenotypic identity in the Victorian highlands over time, and perceptively ‘wild dog’ like animals were more dingo than domestic dog.

As prominent researchers in predator ecology, biology, archaeology, cultural heritage, social science, humanities, animal behaviour and genetics, we emphasise the importance of dingoes in Australian, and particularly Victorian, ecosystems. Dingoes are the sole non-human, land-based, top predator on the Australian mainland. Their importance to the ecological health and resilience of Australian ecosystems cannot be overstated, from regulating wild herbivore abundance (e.g., various kangaroo species), to reducing the impacts of feral mesopredators (cats, foxes) on native marsupials (Johnson & VanDerWal 2009; Wallach et al. 2010; Letnic et al. 20122013; Newsome et al. 2015; Morris & Letnic 2017). Their iconic status is important to First Nations people and to the cultural heritage of all Australians. Read the rest of this entry »