Want to work with us?

22 03 2013
© Beboy-Fotolia

© Beboy-Fotolia

Today we announced a HEAP of positions in our Global Ecology Lab for hot-shot, up-and-coming ecologists. If you think you’ve got what it takes, I encourage you to apply. The positions are all financed by the Australian Research Council from grants that Barry Brook, Phill Cassey, Damien Fordham and I have all been awarded in the last few years. We decided to do a bulk advertisement so that we maximise the opportunity for good science talent out there.

We’re looking for bright, mathematically adept people in palaeo-ecology, wildlife population modelling, disease modelling, climate change modelling and species distribution modelling.

The positions are self explanatory, but if you want more information, just follow the links and contacts given below. For my own selfish interests, I provide a little more detail for two of the positions for which I’m directly responsible – but please have a look at the lot.

Good luck!

CJA Bradshaw

Job Reference Number: 17986 & 17987

The world-leading Global Ecology Group within the School of Earth and Environmental Sciences currently has multiple academic opportunities. For these two positions, we are seeking a Postdoctoral Research Associate and a Research Associate to work in palaeo-ecological modelling. Read the rest of this entry »





Crying ‘wolf’ overlooks the foxes: challenging ‘planetary tipping points’

28 02 2013

tipping pointToday, a paper by my colleague, Barry Brook, appeared online in Trends in Ecology and Evolution. It’s bound to turn a few heads.

Let’s not get distracted by the title of the post, or the potential for a false controversy. It’s important to be clear that the planet is indeed ill, and it’s largely due to us. Species are going extinct faster than the would have otherwise. The planet’s climate system is being severely disrupted, so is the carbon cycle. Ecosystem services are on the decline.

But – and it’s a big ‘but’ – we have to be wary of claiming the end of the world as we know it or people will shut down and continue blindly with their growth and consumption obsession. We as scientists also have to be extremely careful not to pull concepts and numbers out of our bums without empirical support.

Specifically, I’m referring to the latest ‘craze’ in environmental science writing – the idea of ‘planetary tipping points‘ and the related ‘planetary boundaries‘. It’s really the stuff of Hollywood disaster blockbusters – the world suddenly shifts into a new ‘state’ where some major aspect of how the world functions does an immediate about-face. Read the rest of this entry »





The biggest go first

11 12 2012
© James Cameron

© James Cameron

The saying “it isn’t rocket science” is a common cliché in English to state, rather sarcastically, that something isn’t that difficult (with the implication that the person complaining about it, well, shouldn’t). But I really think we should change the saying to “it isn’t ecology”, for ecology is perhaps one of the most complex disciplines in science (whereas rocket science is just ‘complicated’). One of our main goals is to predict how ecosystems will respond to change, yet what we’re trying to simplify when predicting is the interactions of millions of species and individuals, all responding to each other and to their outside environment. It becomes quickly evident that we’re dealing with a system of chaos. Rocket science is following recipes in comparison.

Because of this complexity, ecology is a discipline plagued by a lack of generalities. Few, if any, ecological laws exist. However, we do have an abundance of rules of thumb that mostly apply in most systems. I’ve written about a few of them here on ConservationBytes.com, such as the effect of habitat patch size on species diversity, the importance of predators for maintaining ecosystem stability, and that low genetic diversity doesn’t exactly help your chances of persisting. Another big one is, of course, that in an era of rapid change, big things tend to (but not always – there’s that lovely complexity again) drop off the perch before smaller things do.

The prevailing wisdom is that big species have slower life history rates (reproduction, age at first breeding, growth, etc.), and so cannot replace themselves fast enough when the pace of their environment’s change is too high. Small, rapidly reproducing species, on the other hand, can compensate for higher mortality rates and hold on (better) through the disturbance. Read the rest of this entry »





Malady of numbers

30 07 2012

Organism abundance is the parameter most often requiring statistical treatment. Statistics turn our field/lab notes into estimates of population density after considering the individuals we can see and those we can’t. Later, statistical analyses will relate our density estimates to other factors (climate, demography, genetics, human impacts), allowing the examination of key issues such as extinction risk, biomonitoring or ecosystem services (humus formation, photosynthesis, pollination, fishing, etc.). Photos – top: a patch of fungi (Lacandon Jungle, Mexico), next down: a palm forest (Belize river, Belize), next down: an aggregation of butterflies (Amazon, Peru), and bottom: a group of river dolphins (Amazon, Colombia). Photos by Salvador Herrando-Pérez.

Another interesting and provocative post from my (now ex-) PhD student, Dr. Salvador Herrando-Pérez. After reading this post, you might be surprised to know that Salva was one of my more quantitative students, and although he struggled to keep up with the maths at times, he eventually become quite an efficient ecological modeller (see for yourself in his recent publications here and here).

When an undergraduate faces the prospect of a postgraduate degree (MSc/PhD), he or she is often presented with an overwhelming contradiction: the host university expects the student to have statistical skills for which he/she might never have received instruction. This void in the education system forges professionals lacking statistical expertise, skills that are mandatory for cutting-edge research!

Universities could provide the best of their societal services if, instead of operating in isolation, they integrated the different phases of academic training students go through until they enter the professional world. Far from such integration in the last 20 years, universities have become a genuine form of business and therefore operate competitively. Thus, they seek public and private funding by means of student fees (lecturing), as well as publications and projects developed by their staff (research). In this kind of market-driven academia, we need indicators of education quality that quantify the degree by which early-career training methods make researchers useful, innovative and cost-effective for our societies, particularly in the long term.

More than a century ago, the geologist and educator Thomas Chamberlin (1) distinguished acquisitive from creative learning methods. The former are “an attempt to follow by close imitation the processes of other thinkers and to acquire the results of their investigation by memorising”. The latter represent “the endeavour… to discover new truth or to make a new combination of truth or at least to develop by one’s own effort an individualised assemblage of truth… to think for one’s self”. From the onset of their academic training, students of many countries are instructed in acquisitive methods of learning that reward the retention of information, much of which falls into oblivion after being regurgitated during an exam. Apart from being a colossal waste of resources (because it yields near null individual or societal benefits), this vicious machinery is reinforced by reward and punishment in convoluted manners. For instance, one of my primary-school teachers had boys seated in class by a ‘ranking of intelligence’; so one could lose the first seat if the classmate in the second seat answered a question correctly, which the up-to-then ‘most intelligent’ had failed to hit. Read the rest of this entry »





Biodiversity conservation and behaviour change

23 07 2012

I have been asked by Diogo Veríssimo, a PhD student at the Durrell Institute of Conservation and Ecology (DICE) based at the University of Kent, to post a call for papers for a special issue of Conservation Evidence (details below). I’ve bumped into Diogo at a few conferences, and learnt a few weeks ago that he won the IUCN/Thomson Reuters Environmental Award for his essay entitled Greening the crisis: turning trouble into opportunity. Well done, Diogo.

Dear Colleagues,

I am inviting you to submit case-studies on behaviour change and biodiversity and conservation for a special issue in the journal Conservation Evidence, an online and open-access scientific journal that focuses on project-level conservation interventions with the aim of sharing lessons learned. The aim of this special issue is to document specific conservation interventions that delivered changes in behaviours relevant to the management and conservation of biodiversity and in this way share lessons learned.

Interventions that have not been successful are especially of interest as these allow for an understanding and discussion of what does not work and why. All case studies need to include an evaluation of the impacts of the intervention and are written by, or in partnership with, those who did the conservation work. Read the rest of this entry »





Conservation and Ecology Impact Factors 2011

29 06 2012

Here we go – another year, another set of citations, and another journal ranking by ISI Web of Knowledge Journal Citation Reports. Love them or loathe them, Impact Factors (IF) are immensely important for dictating publication trends. No, a high Impact Factor doesn’t mean your paper will receive hundreds of citations, but the two are correlated.

I’ve previously listed the 2008, 2009 and 2010 IF for major conservation and ecology journals – now here are the 2011 IF fresh off the press (so to speak). I’ve included the 2010 alongside to see how journals have improved or worsened (but take note – journals increase their IF on average anyway merely by the fact that publication frequency is increasing, so small jumps aren’t necessarily meaningful).

Read the rest of this entry »





Arguing for scientific socialism in ecology funding

26 06 2012

What makes an ecologist ‘successful’? How do you measure ‘success’? We’d all like to believe that success is measured by our results’ transformation of ecological theory and practice – in a conservation sense, this would ultimately mean our work’s ability to prevent (or at least, slow down) extinctions.

Alas, we’re not that good at quantifying such successes, and if you use the global metric of species threats, deforestation, pollution, invasive species and habitat degradation, we’ve failed utterly.

So instead, we measure scientific ‘success’ via peer-reviewed publications, and the citations (essentially, scientific cross-referencing) that arise from these. These are blunt instruments, to be sure, but they are really the only real metrics we have. If you’re not being cited, no one is reading your work; and if no one is reading you’re work, your cleverness goes unnoticed and you help nothing and no one.

A paper I just read in the latest issue of Oikos goes some way to examine what makes a ‘successful’ ecologist (i.e., in terms of publications, citations and funding), and there are some very interesting results. Read the rest of this entry »





Costs and benefits of a carbon economy for conservation

12 06 2012

I’ve had the good fortune of being involved now in a several endeavours funded by the Australian Centre for Ecological Analysis and Synthesis (ACEAS); two of those were workshops targeting specific questions regarding estimating modern extinction rates and examining the effects of genetic bottlenecks on Australian biota. The third was a bit different, to say the least – it was a little along the lines of ‘build it, and they will come‘. In other words, what happens when you bung 40 loosely associated researchers in a room for two days? Does anything of substance result, or does it degenerate into a mere talk-fest. I’m happy to say the former. The details of the ACEAS ‘Grand Workshop‘ are now being finalised in a paper that should be submitted by the end of the month. The ACEAS report is reproduced below.

The Grand ACEAS Workshop was something of an experiment: what will happen when we bring 30 of Australia’s top scientists working on land management issues into the same room?

The Grand Workshop participants came from academia, research institutions and the government, and had all received ACEAS funding for working groups. David Keith, Ted Lefroy, Jasmyn Lynch, Wayne Meyer and Dick Williams were amongst the attendees of the two-day workshop.

And when this group of people came together wanting to analyse and synthesise ecological data, great things happened.

“We decided to focus on how carbon pricing legislation will affect land use change and how will that spill over into biodiversity persistence”, said Professor Corey Bradshaw, Director of Ecological Modelling at The University of Adelaide, who led the synthesis activity at the Grand ACEAS Workshop.

“Will carbon pricing lead to good outcomes for biodiversity, or negative ones, or will it have no bearing whatsoever?”

The workshop participants broke into five groups to discuss how the carbon tax legislation will change land use when it is introduced in July 2012, and the potential impact on biodiversity.

Some of the questions asked included:

  • Is it enough simply to allow plants to re-grow to be eligible for carbon credits?
  • How will an increase in forestry plantations impact biodiversity, water catchments and fire regimes?
  • Will there be more kangaroo grazing to reduce methane emissions and erosion, replacing hard-hoofed livestock?
  • Can you receive carbon credits for shooting large feral animals like goats, camels, deer and boars?

The groups found many opportunities for positive biodiversity outcomes with the carbon sequestration activities encouraged by carbon pricing, but there are also many potential ‘bio-perversities’. Read the rest of this entry »





No more ecology

9 05 2012

To all ecology people who read this blog (students, post-docs, academics), this is an intriguing, provocative and slightly worrying title. As ecology has matured into a full-fledged, hard-core, mathematical science on par with physics, chemistry and genetics (and is arguably today one of the most important sciences given how badly we’ve trashed our own home), its sophistication now threatens to render many of the traditional aspects of ecology redundant.

Let me explain.

As a person who cut his teeth in field ecology (with all the associated dirt, dangers, bites, stings, discomfort, thrills, headaches and disasters), I’ve had my fair share of fun and excitement collecting ecological data. There’s something quaintly Victorian (no, I am not referring to the state next door) about the romantic and obsessive naturalist collecting data to the exclusion of nearly all other aspects of civilised life; the intrepid adventurer in some of us takes over (likely influenced by the likes of David Attenborough) and we convince ourselves that our quest for the lonely datum will heal all of the Earth’s ailments.

Bollocks.

As I’ve matured in ecology and embraced its mathematical complexity and beauty, the recurring dilemma is that there are never enough data to answer the really big questions. We have sampled only a fraction of extant species, we know embarrassingly little about how ecosystems respond to disturbance, and we know next to nothing about the complexities of ecosystem services. And let’s not forget our infancy in understanding the synergies of extinctions in the past and projections into the future. Multiply this uncertainty by several orders of magnitude for ocean ecosystems.

Read the rest of this entry »





Unholy trinity of leakage, permanence and additionality

13 03 2012

I begin with the proverbial WTF? The title of this post sounds a little like the legalese accompanying a witchcraft trial, but it’s jargon that’s all the rage in the ‘trading-carbon-for-biodiversity’ circles.

I’m sure that most of my readers will have come across the term ‘REDD‘ (Reduced Emissions from Deforestation and forest Degradation), which is the clever idea of trading carbon credits to keep forests intact. As we know, living forests can suck up a lot of carbon from the atmosphere (remember your high school biology lesson on photosynthesis? Carbon dioxide in. Oxygen out), even though climate change is threatening this invaluable ecosystem service. So the idea of paying a nation (usual a developing country) to protect its forests in exchange for carbon pollution offsets can potentially save two birds with one feeder – reducing overall emissions by keeping the trees alive, and ensuring a lot of associated biodiversity gets caught up in the conservation process.

The problem with REDD though is that it’s a helluva thing to bank on given a few niggly problems essentially revolving around trust. Ah yes, the bugbear of any business transaction. As the carbon credit ‘buyer’ (the company/nation/individual who wishes to offset its carbon output by ‘buying’ the carbon uptake services provided by the intact forest), you’d want to make damn sure that all the money you spend to offset your carbon actually does just that, and that it doesn’t just end up in the hands of some corrupt official, or even worse, used to generate industry that results in even higher emissions! As the buyer, of course you want to entice investors to give you lots of money, and if you bugger up the transaction (by losing the resource you are providing), you’re not likely to have any more investors coming knocking on your door.

Enter the unholy trinity of leakage, permanence and additionality.

This horrible jargon essentially describes the REDD investment problem:

Read the rest of this entry »





Parts a whole do not make

17 02 2012

I’m particularly proud of our latest paper for three main reasons:  (1) Salva Herrando-Pérez, lead author and contributor-extraordinaire to CB, has worked extremely hard to get this one out; (2) it is published in a really good journal; and most importantly, (3) it’s the very first empirical demonstration over hundreds of species that just because you have a density effect on some vital rate (e.g., survival, fertility, dispersal), this in no way means you have any evidence at all for density dependence at the population level. Let us explain.

Quantifying variation in population size is an important element for explaining and predicting population dynamics. In models where a vital (demographic) rate responds to change in population size, those ‘density-dependent’ relationships are ecologically understood as being demographic signals of trophic and social interactions, such as parasitism, predation or competition for shelter, because the intensity of those interactions varies with population size.

In fact, density-dependent effects reflect the theoretical capacity of populations to adjust growth and rebound from low or high numbers – and so this concept has become an important metric in population management and conservation  (Eberhardt et al. 2008). Read the rest of this entry »





More is better

18 01 2012

In one of those rare moments of perusing the latest ecological literature, I stumbled across an absolute gem, and one that has huge conservation implications. Now, I’m really no expert in this particular area of ecology, but I dare say the paper I’m about to introduce should have been published in Nature or Science (I suspect it was submitted to at least one of these journals first). It was still published in an extremely high-impact journal in ecology though – the Journal of Ecology produced by the British Ecological Society (and one in which I too have had the honour of publishing an article).

Before I get into specifics, I have to say that one thing we conservation biologists tend to bang on about is that MORE SPECIES = BETTER, regardless of the ecosystem in question. We tend to value species richness as the gold standard of ecosystem ‘health’ and ‘resilience’, whether or not there is strong empirical evidence in support. It’s as if the more-is-better mantra strikes an intuitive chord and must, by all that’s ecologically right in the world, be true.

Of course, measuring what is ‘better’ is a difficult task, especially when we are talking about complex ecosystems comprising thousands, if not millions, of species. Does ‘better’ refer to the most temporally stable, the most genetically diverse, the most resilient to perturbation, or the provider of the greatest number of functions and hence, ecosystem services?

It’s up to you, but all these things tend to be difficult to measure for a large number of species and over time scales of sufficient duration to measure change. So the default for plants (i.e., the structural framework of almost all ecosystems) I guess has come down to a simpler measure of success – ‘productivity’. This essentially means how much biomass is produced per unit area/volume per time step. It’s not a great metric, but it’s probably one of the more readily quantifiable indices.

Enter the so-called ‘diversity-productivity relationship’, or ‘DPR’, which predicts that higher plant species diversity should engender higher net productivity (otherwise known as the ‘net biodiversity effect’). Read the rest of this entry »





Not magic, but necessary

18 10 2011

In April this year, some American colleagues of ours wrote a rather detailed, 10-page article in Trends in Ecology and Evolution that attacked our concept of generalizing minimum viable population (MVP) size estimates among species. Steve Beissinger of the University of California at Berkeley, one of the paper’s co-authors, has been a particularly vocal adversary of some of the applications of population viability analysis and its child, MVP size, for many years. While there was some interesting points raised in their review, their arguments largely lacked any real punch, and they essentially ended up agreeing with us.

Let me explain. Today, our response to that critique was published online in the same journal: Minimum viable population size: not magic, but necessary. I want to take some time here to summarise the main points of contention and our rebuttal.

But first, let’s recap what we have been arguing all along in several papers over the last few years (i.e., Brook et al. 2006; Traill et al. 2007, 2010; Clements et al. 2011) – a minimum viable population size is the point at which a declining population becomes a small population (sensu Caughley 1994). In other words, it’s the point at which a population becomes susceptible to random (stochastic) events that wouldn’t otherwise matter for a small population.

Consider the great auk (Pinguinus impennis), a formerly widespread and abundant North Atlantic species that was reduced by intensive hunting throughout its range. How did it eventually go extinct? The last remaining population blew up in a volcanic explosion off the coast of Iceland (Halliday 1978). Had the population been large, the small dent in the population due to the loss of those individuals would have been irrelevant.

But what is ‘large’? The empirical evidence, as we’ve pointed out time and time again, is that large = thousands, not hundreds, of individuals.

So this is why we advocate that conservation targets should aim to keep at or recover to the thousands mark. Less than that, and you’re playing Russian roulette with a species’ existence. Read the rest of this entry »





All that glitters is not gold – ecological traps

27 09 2011

Another corker from Salvador Herrando-Pérez:

Cinema fans know that choosing a movie by the newspaper’s commentary or the promotional poster might be a lottery. In the movie of nature, to confuse ‘the attractive’ with ‘the appropriate’ can compromise the life of an individual and its offspring, even to the extent of anticipating the extinction of an entire population or species.

Animals make daily choices about when, where or with whom to engage in basic activities like eating, hibernating, mating, migrating or resting. Those choices are often strongly tied to highly specific cues – e.g., air temperature, tree density, location of water, or smell of other individuals. And it happens to hair lice jumping from head to head among school kids, or to caribou forming their winter herds prior to the seasonal migration. All species, without exception, persist in nature because those ‘choices’ translate into survival or successful reproduction more often than do not. They are a kind of evolutionary memory imprinted in an organism’s genes and behaviour. However, sometimes the right choice (‘right’ meaning perceiving a cue for the role it actually has in the life cycle) places an individual in the worst of all possible situations. The environment cheats, ‘the attractive’ merely mimics ‘the appropriate’, and the individual fails to reproduce, starves, sickens, or even dies.

Figure 1. Water reservoirs tainted with fuel (see dark contours) in Kuwait following the Gulf War in the early 1990s. Overlaid pictures show the silhouettes of trapped odonates (right), vertebrates (top left) and invertebrates (bottom left) (Photos courtesy of Jochen Zeil).

At the mercy of mirages

During the Gulf War, the destruction of infrastructure for crude exploitation spilled large amounts of fuel in many water reservoirs over the desert landscape of Kuwait. A little later, Horváth and Zeil1 found agglomerations of dead insects (and a range of vertebrates) along the shores of these polluted reservoirs, and observed dragonflies drowning in their kamikaze attempt to spawn on the oily surface (Figure 1). This work stimulated further research whereby Horváth and his team in Budapest showed that odonates are attracted by light polarization at the surface of oiled water2 – hence ‘polarized light pollution’3. Not only that, they recorded insects struggling to spawn on or mate with riveting surfaces such as solar panels, asphalted roads, plastic bags or (creepy enough!) cemetery crypts4. It goes without saying: these insects are victims of a mirage.

Those habitats or features of the habitat that mislead an animal’s choice, often hampering the completion of its life cycle, are known as ‘ecological traps’ – in other words, the environmental cue is decoupled from the quality of the habitat it is meant to signal. Ecological traps were first described in the 1970s by Dwernychuk and Boag5. They found that ducks on the islands of Miquelon lake located their nests among those of seagulls despite the latter happily devoured their ducklings and eggs. When these islands emerged in the middle of last century, they were first colonized by common terns (Sterna hirundo). By defending their own nests ferociously from predators (mainly crows and magpies), the terns inadvertently shielded the nests of their ducky comrades. The Canadians hypothesized that when seagulls subsequently replace terns, the ducks continued to sense their new neighbours as a (now misleading) sign of protection. Read the rest of this entry »





Life, death and Linneaus

9 07 2011

Barry Brook (left) and Lian Pin Koh (right) attacking Fangliang He (centre). © CJA Bradshaw

I’m sitting in the Brisbane airport contemplating how best to describe the last week. If you’ve been following my tweets, you’ll know that I’ve been sequestered in a room with 8 other academics trying to figure out the best ways to estimate the severity of the Anthropocene extinction crisis. Seems like a pretty straight forward task. We know biodiversity in general isn’t doing so well thanks to the 7 billion Homo sapiens on the planet (hence, the Anthropo prefix) - the question though is: how bad?

I blogged back in March that a group of us were awarded a fully funded series of workshops to address that question by the Australian Centre for Ecological Synthesis and Analysis (a Terrestrial Ecosystem Research Network facility based at the University of Queensland), and so I am essentially updating you on the progress of the first workshop.

Before I summarise our achievements (and achieve, we did), I just want to describe the venue. Instead of our standard, boring, windowless room in some non-descript building on campus, ACEAS Director, Associate Professor Alison Specht, had the brilliant idea of putting us out away from it all on a beautiful nature-conservation estate on the north coast of New South Wales.

What a beautiful place – Linneaus Estate is a 111-ha property just a few kilometres north of Lennox Head (about 30 minutes by car south of Byron Bay) whose mission is to provide a sustainable living area (for a very lucky few) while protecting and restoring some pretty amazing coastal habitat along an otherwise well-developed bit of Australian coastline. And yes, it’s named after Carl Linnaeus. Read the rest of this entry »





2010 ISI Impact Factors out now (with some surprises)

29 06 2011

It’s been another year of citations and now the latest list of ISI Impact Factors (2010) has come out. Regardless of how much stock you put in these (see here for a damning review), you cannot ignore their influence on publishing trends and author journal choices.

As I’ve done for 2008 and 2009, I’ve taken the liberty of providing the new IFs for some prominent conservation and ecology journals, and a few other journals occasionally publishing conservation-related material.

One particular journal deserves special attention here. Many of you might know that I was Senior Editor with Conservation Letters from 2008-2010, and I (with other editorial staff) made some predictions about where the journal’s first impact factor might be on the scale (see also here). Well, I have to say the result exceeded my expectations (although Hugh Possingham was closer to the truth in the end – bugger!). So the journal’s first 2010 impact factor (for which I take a modicum of credit ;-) is a whopping… 4.694 (3rd among all ‘conservation’ journals). Well done to all and sundry who have edited and published in the journal. My best wishes to the team that has to deal with the inevitable rush of submissions this will likely bring!

So here are the rest of the 2010 Impact Factors with the 2009 values for comparison: Read the rest of this entry »





The rarity paradox

22 06 2011

© C. Madden

My friend and colleague at the Centre National de Recherche Scientfique (CNRS), Laboratoire d’Ecologie Systématique & Evolution based at the Université Paris-Sud in France, Dr. Franck ‘Allee EffectCourchamp, has asked me to help him out finding a suitable candidate for what sounds like a very cool job. If you’re in the market for a very interesting and highly relevant conservation post-doctoral fellowship, please read on.

And even if you’re not looking for a position, but are interested in the anthropogenic Allee effect, then by all means, please read on as well.

This two-year fellowship is part of a grant focused on demonstrating the novel rarity paradox, either in new wildlife trade markets (i.e., exotic pets, traditional medicine, et cetera) or in newly exploited species (e.g., tibetan antilope, seahorses, et cetera). Read the rest of this entry »





生态学 = ‘Ecology’ in China

13 05 2011

I’m just heading home after a very inspiring workshop organised by Fangliang He at Sun Yat-sen University in Guangzhou, China (I’m writing this from the Qantas Club in the Hong Kong airport).

Before I proceed to regale you with the salient details of the ‘International Symposium for Biodiversity and Theoretical Ecology‘, I am compelled to state publicly that I offer my sincerest condolences to Fangliang and his family; unfortunately Fangliang’s brother passed away while we were at the workshop and so Fangliang wasn’t able to spend much time reaping the fruits of his organisational labour. If you know Fangliang, please send him a supporting email.

That sad note aside, I am delighted to say that the workshop was compelling, challenging and also rather fortuitous. I was one of many overseas invitees, and I must say that I was at times overwhelmed by the size of the brains they managed to pack into the auditorium. Many colleagues I didn’t know attended, and I hope that many will become collaborators. The international invitees were: Read the rest of this entry »





Resolving the Environmentalist’s Paradox

7 04 2011

Here’s an extremely thought-provoking guest post by Megan Evans, Research Assistant at the University of Queensland in Kerrie Wilson‘s lab. Megan did her Honours degree with Hugh Possingham and Kerrie, and has already published heaps from that and other work. I met Megan first in 2009 and have been extremely impressed with her insights, broad range of interests and knowledge, and her finely honed grasp of social media in science. Smarter than your average PhD student, without a doubt (and she has even done one yet). Take it away, Megan.

© T. Toles

Resolving the ‘Environmentalist’s Paradox’, and the role of ecologists in advancing economic thinking

Aldo Leopold famously described the curse of an ecological education as “to be the doctor who sees the marks of death in a community that believes itself well and does not want to be told otherwise”. Ecologists do have a tendency for making dire warnings for the future, but for anyone concerned about the myriad of problems currently facing the Earth – climate change, an ongoing wave of species extinctions and impending peak oil, phosphate, water , (everything?) crises – the continued ignorance or ridicule of such warnings can be a frustrating experience. Environmental degradation and ecological overshoot isn’t just about losing cute plants and animals, given the widespread acceptance that long-term human well-being ultimately rests on the ability for the Earth to supply us with ecosystem services.

In light of this doom and gloom, things were shaken up a bit late last year when an article1 published in Bioscience pointed out that in spite of declines in the majority of ecosystem services considered essential to human well-being by The Millenium Ecosystem Assessment (MA), aggregate human well-being (as measured by the Human Development Index) has risen continuously over the last 50 years. Ciara Raudsepp-Hearne and the co-authors of the study suggested that these conflicting trends presented an ‘environmentalist’s paradox’ of sorts – do we really depend on nature to the extent that ecologists have led everyone to believe? Read the rest of this entry »





How fast are we losing species anyway?

28 03 2011

© W. Laurance

I’ve indicated over the last few weeks on Twitter that a group of us were recently awarded funding from the Australian Centre for Ecological Synthesis and Analysis – ACEAS – (much like the US version of the same thing – NCEAS) to run a series of analytical workshops to estimate, with a little more precision and less bias than has been done previously, the extinction rates of today’s biota relative to deep-time extinctions.

So what’s the issue? The Earth’s impressive diversity of life has experienced at least five mass extinction events over geological time. Species’ extinctions have kept pace with evolution, with more than 99 % of all species that have ever existed now gone (Bradshaw & Brook 2009). Despite general consensus that biodiversity has entered the sixth mass extinction event because of human-driven degradation of the planet, estimated extinction rates remain highly imprecise (from 100s to 10000s times background rates). This arises partly because the total number of species is unknown for many groups, and most extinctions go unnoticed.

So how are we going to improve on our highly imprecise estimates? One way is to look at the species-area relationship (SAR), which to estimate extinction requires one to extrapolate back to the origin in taxon- and region-specific SARs (e.g., with a time series of deforestation, one can estimate how many species would have been lost if we know how species diversity changes in relation to habitat area). Read the rest of this entry »








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