When the cure becomes the disease

6 02 2012

I’ve always barracked for Peter Kareiva‘s views and work; I particularly enjoy his no-bullshit, take-no-prisoners approach to conservation. Sure, he’s said some fairly radical things over the years, and has pissed off more than one conservationist in the process. But I think this is a good thing.

His main point (as is mine, and that of a growing number of conservation scientists) is that we’ve already failed biodiversity, so it’s time to move into the next phase of disaster mitigation. By ‘failing’ I mean that, love it or loathe it, extinction rates are higher now than they have been for millennia, and we have very little to blame but ourselves. Apart from killing 9 out of 10 people on the planet (something no war or disease will ever be able to do), we’re stuck with the rude realism that it’s going to get a lot worse before it gets better.

This post acts mostly an introduction to Peter Kareiva & collaborators’ latest essay on the future of conservation science published in the Breakthrough Institute‘s new journal. While I cannot say I agree with all components (especially the cherry-picked resilience examples), I fundamentally support the central tenet that we have to move on with a new state of play.

In other words, humans aren’t going to go away, ‘pristine’ is as unattainable as ‘infinity’, and reserves alone just aren’t going to cut it. 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 »





When did it go extinct?

11 01 2012

It was bound to happen. After years of successful avoidance I have finally succumbed to the dark side: palaeo-ecology.

I suppose the delve from historical/modern ecology into prehistory was inevitable given (a) my long-term association with brain-the-size-of-a-planet Barry Brook (who, incidentally, has reinvented his research career many times) and (b) there is no logic to contend that palaeo extinction patterns differ in any meaningful way from modern biodiversity extinctions (except, of course, that the latter are caused mainly by human endeavour).

So while the last, fleeting days of my holiday break accelerate worringly toward office-incarceration next week, I take this moment to present a brand-new paper of ours that has just come out online in (wait for it) Quaternary Science Reviews entitled Robust estimates of extinction time in the geological record.

Let me explain my reasons for this strange departure.

It all started after a few drinks (doesn’t it always) with Alan Cooper, Chris Turney and Barry Brook when we were discussing the uncertainties associated with the timing of megafauna extinctions – you might be aware that traditionally there have been two schools of thought on late-Pleistocene extinction pulses: (1) those who think there were mainly caused by massive climate shifts not to dissimilar to what we are experiencing now and (2) those who believe that the arrival of humans into naïve regions lead to a ‘blitzkrieg‘ of hunting and overkill. Rarely do adherents of each stance agree (and sometimes, the ‘debate’ can get ugly given the political incorrectness of inferring that prehistoric peoples were as destructive as we are today – cf. the concept of the ‘noble savage‘). Read the rest of this entry »





Cartoon guide to biodiversity loss XIV

30 12 2011

The last post of 2011, I thought I’d focus on the lighter side (that is to say, my brain is muddled by the lovely break from academia, so I don’t really feel like investing too much cerebral energy). Here, therefore, are the latest six cartoons… (see full stock of previous ‘Cartoon guide to biodiversity loss’ compendia here). May fewer species go extinct in 2012 than 2011…

Read the rest of this entry »





Slicing the second ‘lung of the planet’

12 12 2011

© WWF

Apologies for the slow-down in postings this past week – as many of you know, I was attending the International Congress for Conservation Biology in Auckland. I’ll blog about the conference later (and the stoush that didn’t really occur), but suffice it to say it was very much worthwhile.

This post doesn’t have a lot to do per se with the conference, but it was stimulated by a talk I attended by Conservation Scholar Stuart Pimm. Now, Stuart is known mainly as a tropical conservation biologist, but as it turns out, he also is a champion of temperate forests – he even sits on the science panel of the International Boreal Conservation Campaign.

I too have dabbled in boreal issues over my career, and most recently with a review published in Trends in Ecology and Evolution on the knife-edge plight of boreal biodiversity and carbon stores. That paper was in fact the result of a brain-storming session Navjot Sodhi and I had one day during my visit to Singapore sometime in 2007. We thought, “It doesn’t really seem that people are focussing their conservation attention on the boreal forest; how bad is it really?”.

Well, it turns out that the boreal forest is still a vast expanse and that there aren’t too many species in imminent danger of extinction; however, that’s where the good news ends. The forest itself is becoming more and more fragmented from industrial development (namely, forestry, mining, petroleum surveying and road-building) and the fire regime has changed irrevocably from a combination of climate change and intensified human presence. You can read all these salient features here.

So, back to my original thread – Stuart gave a great talk on the patterns of deforestation worldwide, with particular emphasis on how satellite imagery hides much of the fine-scale damage that we humans do to the world’s great forests. It was when he said (paraphrased) that “50,000 km2 of boreal forest is lost each year, but even that statistic hides a major checkerboard effect” that my interest was peaked. Read the rest of this entry »





Better SAFE than sorry

30 11 2011

http://goo.gl/KZ50o

Last day of November already – I am now convinced that my suspicions are correct: time is not constant and in fact accelerates as you age (in mathematical terms, a unit of time becomes a progressively smaller proportion of the time elapsed since your birth, so this makes sense). But, I digress…

This short post will act mostly as a spruik for my upcoming talk at the International Congress for Conservation Biology next week in Auckland (10.30 in New Zealand Room 2 on Friday, 9 December) entitled: Species Ability to Forestall Extinction (SAFE) index for IUCN Red Listed species. The post also sets a bit of the backdrop to this paper and why I think people might be interested in attending.

As regular readers of CB will know, we published a paper this year in Frontiers in Ecology and the Environment describing a relatively simple metric we called SAFE (Species Ability to Forestall Extinction) that could enhance the information provided by the IUCN Red List of Threatened Species for assessing relative extinction threat. I won’t go into all the detail here (you can read more about it in this previous post), but I do want to point out that it ended up being rather controversial.

The journal ended up delaying final publication because there were 3 groups who opposed the metric rather vehemently, including people who are very much in the conservation decision-making space and/or involved directly with the IUCN Red List. The journal ended up publishing our original paper, the 3 critiques, and our collective response in the same issue (you can read these here if you’re subscribed, or email me for a PDF reprint). Again, I won’t go into an detail here because our arguments are clearly outlined in the response.

What I do want to highlight is that even beyond the normal in-print tête-à-tête the original paper elicited, we were emailed by several people behind the critiques who were apparently unsatisfied with our response. We found this slightly odd, because many of the objections just kept getting re-raised. Of particular note were the accusations that: Read the rest of this entry »





Supercharge Your Science V.2

24 11 2011

http://goo.gl/ogdT8

I suspect a lot of ConservationBytes.com readers will be attending the imminent 25th International Congress for Conservation Biology to be held in Auckland from 5-9 December 2011 (it was to be held in Christchurch, but the venue was changed after that city fell down). I’ve now been to 3 previous ICCBs myself, and it should prove to be a good, informative (and fun) meeting.

I’ll be giving a talk or two, as will some of my students and postdocs, but I’m not spruiking those here (but you’re all invited, of course).

The main reason for this short post today is to advertise for Version 2 of our (i.e., Bill Laurance and me) popular ‘Supercharge Your Science‘ workshop. Yes, the organising committee of the ICCB decided it was a good idea to accept our application to repeat our previously successful series of presentations extolling the virtues of positive and controlled media interactions, social media and good writing techniques for ‘supercharging’ the impact of one’s science. You can read more about the content of this workshop here and here.

The description of the workshop (to be held from 19.00 – 21.00 on 6 December in the SkyCity venue) on the ICCB website is: Read the rest of this entry »





Marine forests dropping off the edge

21 11 2011

© B Murch http://goo.gl/wxvxF

This is probably a little late in terms of breaking news, but it’s good fodder for a blog post nonetheless.

I’ve done several posts now on the value (and threats) of marine macroalgae (seaweeds) – the last one hinted that a major paper was imminent regarding the fate of one of the world’s most important centres of macroalgae diversity in response to our rapidly changing climate: southern Australia.

Well, that paper has now come out in the eminent journal Current Biology headed by that crazy Aussie-Viking phycologist, Dr. Thomas Wernberg (byline here: Thomas was just awarded an Australian Research Council Future Fellowship and deserves many congratulations – not least for which the audacity to wear yellow budgie smugglers in public).

Entitled simply “Seaweed communities in retreat from ocean warming“, the short paper belies a hell of a lot of work examining over 60 years of herbarium records indicating MASSIVE shifts in the macroalgae community southwards on both the east and west coasts of Australia (see some media spots here). What do I mean by ‘massive’? Well, about 300 species on average (52 examined in most detail) shifted about 200 km south on the east coast (where warming has been most pronounced), and about 50 km south on the west coast. Read the rest of this entry »





Mucking around the edges

8 11 2011

Barry Brook over at BraveNewClimate.com beat me to the punch regarding our latest paper, so I better get off my arse and write my take on things.

This post is about a paper we’ve just had accepted and has come out online in Biological Conservation called Strange bedfellows? Techno-fixes to solve the big conservation issues in southern Asia - and it’s likely to piss off a few people, and hopefully motivate others.

We wrote the paper for a special issue of essays dedicated to the memory of our mate and colleague, Navjot Sodhi, who died earlier this year. The issue hasn’t been released yet, but we have managed to get our paper out well before.

Like Navjot, the paper is controversial. Also like Navjot, we hope it challenges a few minds and pushes a few boundaries. We, as conservation biologists, must accept the fact that we have largely failed – biodiversity is still being lost at an alarming rate despite decades and decades of good science, sound evidence-based policy recommendations and even some rescues of species on the ‘brink’. Huge consumption rates, a population of 7 billion humans and counting, carbon emissions exceeding all worst-case scenarios, and greater disparity of wealth distribution have all contributed to this poor performance.

So what else can we do? 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 »





Twenty landmark papers in biodiversity conservation

13 10 2011

While I can’t claim that this is the first time one of my peer-reviewed papers has been inspired by ConservationBytes.com, I can claim that this is the first time a peer-reviewed paper is derived from the blog.

After a bit of a sordid history of review (isn’t it more and more like that these days?), I have the pleasure of announcing that our paper ‘Twenty landmark papers in biodiversity conservation‘ has now been published as an open-access chapter in the new book ‘Research in Biodiversity – Models and Applications‘ (InTech).

Perhaps not the most conventional of venues (at least, not for me), but it is at the very least ‘out there’ now and freely available.

The paper itself was taken, modified, elaborated and over-hauled from text written in this very blog – the ‘Classics‘ section of ConservationBytes.com. Now, if you’re an avid follower of CB, then the chapter won’t probably represent anything terribly new; however, I encourage you to read it anyway given that it is a vetted overview of possibly some of the most important papers written in conservation biology.

If you are new to the field, an active student or merely need a ‘refresher’ regarding the big leaps forward in this discipline, then this chapter is for you.

The paper’s outline is as follows: Read the rest of this entry »





1 million hectares annually – the forest destruction of Indonesia

30 09 2011

© A. Kenyon http://goo.gl/UpG3m

Bill Laurance wrote a compelling and very dour piece in The Conversation this week. He asked for some ‘link love’, so I decided to reproduce the article here for ConservationBytes.com readers. Full credit to Bill and The Conversation, of course.

What comes to mind when you think of Indonesia?

For biologists like myself, Australia’s northern neighbour provokes visions of ancient rainforests being razed by slash-and-burn farmers, and endangered tigers and orangutans fleeing from growling bulldozers.

This reality is true, but there is also hope on the horizon.

Indonesia is a vast, sprawling nation, spanning some 17,000 islands. Among these are Java, Sumatra, half of New Guinea and much of Borneo.

Some of the planet’s most biologically rich and most endangered real estate is found on this archipelago.

Today, Indonesia is losing around 1.1 million hectares of forest annually. That’s an area a third the size of Belgium, bigger than Australia’s Wet Tropics World Heritage Area.

With forest loss now slowing in Brazil, Indonesia has the dubious distinction of being the world’s deforestation “leader”. No nation is destroying its forests faster.

In Sumatra, where I visited recently, the world’s biggest paper-pulp corporations are chopping down hundreds of thousands of hectares of native rainforest to make paper and cardboard.

Some of these corporations also fund aggressive lobbyists, such as World Growth in Washington DC [CJA Bradshaw's note: see our piece on one particular patron of WG - Alan Oxley], to combat their critics and dissuade major retail chains from dropping their products. Read the rest of this entry »





Rise of the phycologists

22 09 2011

Dead man's fingers (Codium fragile) - © CJA Bradshaw

I’ve had an interesting week. First, it’s been about 6 years since I was last in Japan, and I love coming here; the food is exquisite, the people are fantastic (polite, happy, accommodating), everything works (trains, buses, etc.) and most importantly, it has an almost incredible proportion of its native forests intact.

But it wasn’t for forests that I travelled to Japan (nor the sumo currently showing on the guest-room telly where I’m staying – love the sumo): I was here for a calcareous macroalgae workshop.

What?

First, what are ‘macroalgae’, and why are some ‘calcareous’? And why should anyone in their right mind care?

Good questions. Answers: 1. Seaweeds; 2. Many incorporate calcium carbonate into their structures as added structural support; 3. Read on.

Now, I’m no phycologist (seaweed scientist), but I’m fascinated by this particular taxon. I’ve written a few posts about their vital ecological roles (see here and here), but let me regale you with some other important facts about these amazing species.

Some Japanese macroalgae - © CJA Bradshaw

There are about 12,000 known species of macroalgae described by phycologists, but as I’ve learnt this week, this is obviously a vast underestimate. For most taxa that people are investigating now using molecular techniques, the genetic diversity is so high and so geographically structured that there are obviously a huge number of ‘cryptic’ species within our current taxonomic divisions. This could mean that we’re out by up to a factor of 2 in the number of species in the world.

Another amazing fact – about 50 % of all known seaweed species are found in just two countries – Japan and Australia (hence the workshop between Japanese and Australian phycologists). Southern Australia in particular is an endemism hotspot.

Ok. Cool. So far so good. But so what? Read the rest of this entry »





No substitute for primary forest

15 09 2011

© Romulo Fotos http://goo.gl/CrAsE

A little over five years ago, a controversial and spectacularly erroneous paper appeared in the tropical ecology journal Biotropica, the flagship journal of the Association for Tropical Biology and Conservation. Now, I’m normally a fan of Biotropica (I have both published there several times and acted as a Subject Editor for several years), but we couldn’t let that paper’s conclusions go unchallenged.

That paper was ‘The future of tropical forest species‘ by Joseph Wright and Helene Muller-Landau, which essentially concluded that the severe deforestation and degradation of tropical forests was not as big a deal as nearly all the rest of the conservation biology community had concluded (remind you of climate change at all?), and that regenerating, degraded and secondary forests would suffice to preserve the enormity and majority of dependent tropical biodiversity.

What rubbish.

Our response, and those of many others (including from Toby Gardner and colleagues and William Laurance), were fast and furious, essentially destroying the argument so utterly that I think most people merely moved on. We know for a fact that tropical biodiversity is waning rapidly, and in many parts of the world, it is absolutely [insert expletive here]. However, the argument has reared its ugly head again and again over the intervening years, so it’s high time we bury this particular nonsense once and for all.

In fact, a few anecdotes are worthy of mention here. Navjot once told me one story about the time when both he and Wright were invited to the same symposium around the time of the initial dust-up in Biotropica. Being Navjot, he tore off strips from Wright in public for his outrageous and unsubstantiated claims – something to which Wright didn’t take too kindly.  On the way home, the two shared the same flight, and apparently Wright refused to acknowledge Navjot’s existence and only glared looks that could kill (hang on – maybe that had something to do with Navjot’s recent and untimely death? Who knows?). Similar public stoushes have been chronicled between Wright and Bill Laurance.

Back to the story. I recall a particular coffee discussion at the National University of Singapore between Navjot Sodhi (may his legacy endure), Barry Brook and me some time later where we planned the idea of a large meta-analysis to compare degraded and ‘primary’ (not overly disturbed) forests. The ideas were fairly fuzzy back then, but Navjot didn’t drop the ball for a moment. He immediately went out and got Tien Ming Lee and his new PhD student, Luke Gibson, to start compiling the necessary studies. It was a thankless job that took several years.

However, the fruits of that labour have now just been published in Nature: ‘Primary forests are irreplaceable for sustaining tropical biodiversity‘, led by Luke and Tien Ming, along with Lian Pin Koh, Barry Brook, Toby Gardner, Jos Barlow, Carlos Peres, me, Bill Laurance, Tom Lovejoy and of course, Navjot Sodhi [side note: Navjot died during the review and didn't survive to hear the good news that the paper was finally accepted].

Using data from 138 studies from Asia, South America and Africa comprising 2220 pair-wise comparisons of biodiversity ‘values’ between forests that had undergone some sort of disturbance (everything from selective logging through to regenerating pasture) and adjacent primary forests, we can now hammer the final nails into the coffin containing the putrid remains of Wright and Muller-Landau’s assertion – there is no substitute for primary forest. Read the rest of this entry »





Gone with the birds

1 09 2011

ebaumsworld.com

Another great post by Salvador Herrando-Pérez.

Through each new species, evolution assembles a unique combination of genes. Ever since living forms have populated our planet (> 3 billion years), the number of combinations is incalculable. That is why evolution resembles a cocktail shaker. Contemporaneous biogeographers look for order in that shaker to explain the history of life, as much as historians look for monarchs and revolutions in a library to explain the history of humanity.

The ethnic diversity of our suburb, village or city obeys factors of different temporal extent. Recent factors such as wealth, politics (war, segregation), culture (tradition, religion), and technology (airplanes, bridges, tunnels) determine racial migration, mixing and extinction. On the other hand, pre-historical factors express the expansion of the earliest hominids from Africa to the other continents – what makes a bantu ‘bantu’, or an inuit ‘inuit’.

Present ecological conditions and the macro-evolutionary past stock the elements by which biogeography attempts to understand the mechanisms shaping the spatial distribution of species, e.g., why kangaroos are restricted to Oceania, or why you could believe you were in Spain while strolling through a Greek forest. Read the rest of this entry »





Cartoon guide to biodiversity loss XIII

17 08 2011

The latest six cartoons… (see full stock of previous ‘Cartoon guide to biodiversity loss’ compendia here).

Read the rest of this entry »





Drive the future of biodiversity research

20 07 2011

My colleague, Professor Alan Cooper of the Australian Centre for Ancient DNA, has a few funky PhD positions available in high-tech biodiversity applications.

We are looking for interested graduate students, who are highly motivated and enjoy independent and unusual research in the general areas below. An interest in evolution and natural history are key requirements, and a background in any of the following would be useful: evolution, genetics, molecular biology, chemistry/biochemistry and environmental science.

Environmental Genomics

New genomic approaches for biodiversity studies of environmental samples: a number of PhD positions are available in a large-scale project to apply high throughput sequencing approaches to the analysis of environmental samples and develop a new range of methods to perform biodiversity surveys, taxonomic discovery, and environmental impact reports. The project will employ multiplexed PCR, 2nd/3rd-gen sequencing, bioinformatics and Phylogenetics to develop novel systems for rapid and accurate biodiversity assessment. Key topics within the project are the analysis of natural and re-use water supplies, monitoring presence and abundance of threatened species and Australian native grasses. A strong molecular biology and/or bioinformatics background is required. The project is a AU$1M Australian Research Council-industry partnership. 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 »





Taxonomy in the clouds

4 07 2011

Another post (see previous here, here and here) by my aspiring science-communicator PhD student, Salvador Herrando-Pérez.

Taxonomy uses rigorous rules of nomenclature to classify living beings, so every known species has a given ‘name’ and ‘surname’. The revision of certain taxonomic groups (particularly through genetic analyses) is favouring the proliferation of nominally new species, often propelled by virtue of their charisma and conservation status.

In secondary school, most of my classmates associated the subject ‘Biology’ with unpronounceable Latin taxonomic names, with which all known living beings are branded — ‘Canis lupus’ reads the identity card of humanity’s best friend. When the Swedish monk Carl Linnaeus proposed such binomial nomenclature, he could hardly imagine that, two hundred years later, his terminology would underpin national and transnational budgets for species conservation. Taxonomic nomenclature allows the classification of species into clusters of the same kind (e.g., diatoms, amanitas, polychaetes, skinks), and the calculation of an indispensable figure for conservation purposes: how many species are there at a given location, range, country, continent, or the entire planet?

Traditionally, taxonomists described species by examining their (external and internal) morphological features, the widest consensus being that two individuals of different species could not hybridise. However, a practical objection to that thinking was that if, for instance, an ocean separated two leopard populations, ethics should prevent us from bringing them in contact only to check if they produce fertile offspring, hence justifying a common-species status. Genetics currently provides a sort of ‘remote check’.

New species, new names

Over the last three decades, the boom of genetics and the global modernisation of environmental policies have fostered alternative criteria to differentiate species, populations, and even individuals. As a result, experts have created a colourful lexicon to label management or conservation units or new taxonomical categories such as that of a subspecies1, e.g., Canis lupus dingo for the wild Australian dog (dingo). These changes have shaken the foundations of taxonomy because several definitions of species (biological, phylogenetic, evolutionary) are forced to live under the umbrella of a common nomenclature. Read the rest of this entry »





Know thy threat

9 06 2011

Here’s another great guest post by Megan Evans of UQ – her previous post on resolving the environmentalist’s paradox was a real hit, so I hope you enjoy this one too.

The reasons for the decline of Australia’s unique biodiversity are many, and most are well known. Clearing of vegetation for urban and agricultural land uses, introduced species and changed fire patterns are regularly cited in State of the Environment reports, recovery plans and published studies as major threats to biodiversity. But, while these threats are widely acknowledged, little has been done to quantify them in terms of the proportion of species affected, or their spatial extent at a national, state or local scale. To understand why such information on threats may be useful, consider for instance how resources are allocated in public health care1.

Threat knowledge

Conditions such as cancer, heart disease and mental health are regarded as National Health Priority Areas in Australia, and have been given special attention when prioritising funds since the late 1980s. The burden of disease in these priority areas are quantified according to the incidence or prevalence of disease or condition, and its social and economic costs. Estimates of burden of disease and their geographic distribution (often according to local government areas) can assist in communicating broad trends in disease burden, but also in prioritising efforts to achieve the best outcomes for public health. An approach similar to that used in healthcare could help to identify priorities for biodiversity conservation – using information on the species which are impacted by key threats, the spatial distributions of species and threats, and the costs of implementing specific management actions to address these threats. Read the rest of this entry »








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