Put the bite back into biodiversity conservation

2 07 2010

Today’s guest post is by Dr. Euan Ritchie, formerly of James Cook University, but who is now firmly entrenched at Deakin University in Victoria as a new Lecturer in ecology. Euan’s exciting research over the course of his memorable PhD (under the tutelage of renowned ecologist-guru, Professor Chris Johnson) has produced some whoppingly high-impact research. This latest instalment highlights a series of related papers he and his colleagues have just produced. We’re fortunate he agreed to give us his thoughts. Interestingly, the topic was just highlighted in the last issue of NatureDon’t damage dingos.

Corey has invited me to report on a recent paper published in Ecology Letters and another related study in PloS One, which together show how a better understanding of dingoes and their social structure and associated behaviour can help us to maintain or improve the health of our terrestrial ecosystems. This work, led by PhD student Arian Wallach (University of Adelaide), and involving collaborations with John Read (University of Adelaide), Adam O’Neill (C&A Environmental Services) and Christopher Johnson and me (James Cook University), offers some of the strongest evidence yet of the key roles top predators play in maintaining the balance.

Invasive species, along with habitat loss and the impacts of climate change, are among the greatest threats to the continued survival of many species. Because of this, millions of dollars and time is spent each year to control their populations. The impacts of invasive species in Australia are sadly all too obvious, with nearly half of the world’s mammal extinctions in the last 200 years occurring in Australia, with the prime suspects being the introduced domestic cat and red fox. However, despite massive, costly and ongoing attempts to control fox and cat populations successfully, we continue to witness the decline of many of our native species. Why? We would argue that the problem is that for too long much of our conservation and management efforts have been focused on treating symptoms and not the cause, which is the loss of ecosystem resilience (the natural ability of ecosystems to withstand change).

Read the rest of this entry »





Biodiversity SNAFU in Australia’s Jewel

16 06 2010

I’ve covered this sad state of affairs and one of Australia’s more notable biodiversity embarrassments over the last year (see Shocking continued loss of Australian mammals and Can we solve Australia’s mammal extinction crisis?), and now the most empirical demonstration of this is now published.

The biodiversity guru of Australia’s tropical north, John Woinarksi, has just published the definitive demonstration of the magnitude of mammal declines in Kakadu National Park (Australia’s largest national park, World Heritage Area, emblem of ‘co-management’ and supposed biodiversity and cultural jewel in Australia’s conservation crown). According to Woinarski and colleagues, most of those qualifiers are rubbish.

The paper published in Wildlife Research is entitled Monitoring indicates rapid and severe decline of native small mammals in Kakadu National Park, northern Australia and it concludes:

The native mammal fauna of Kakadu National Park is in rapid and severe decline. The cause(s) of this decline are not entirely clear, and may vary among species. The most plausible causes are too frequent fire, predation by feral cats and invasion by cane toads (affecting particularly one native mammal species).

I’ve done quite a bit of work in Kakadu myself, and the one thing that hits you every time you travel through it is the lack of visible wildlife. Sure, you’ll see horses, pigs and buffalo, as well as cane toads and cats, but getting a glimpse of anything native, from Conilurus to Varanus, and you’d consider yourself extremely lucky.

We’ve written a lot about the feral animal problem in Kakadu and even developed software tools to assist in density-reduction programmes. It doesn’t appear that anyone is listening.

Another gob-smacking vista you’ll get when travelling through Kakadu any time from April to December is that it’s either been burnt, actively burning or targeted for burning. They burn the shit out of the place every year. No wonder the native mammals are having such a hard time.

Combine all this with the dysfunctional management arrangement, and you cease to have a National Park. Kakadu is now a lifeless shell that does precious little for conservation of biodiversity (and 3 of the 5 criteria it had to satisfy to become a World Heritage Area are specifically related to natural resource ‘values’). I say, delist Kakadu now and let’s stop fooling ourselves.

Ok, back from the rant. Woinarski and others superimposed a mammal monitoring programme over top a fire-regime experiment for vegetation. Although they couldn’t sample every plot every season, they staggered the sampling to cover the area as best they could over the 13 years of monitoring (1996-2009). What they observed was staggering. Read the rest of this entry »





Australian Ecology Research Award

7 06 2010

I had the immense pleasure of receiving a telephone call a few weeks back from the Ecological Society of Australia telling me that I had been awarded the 2010 Australian Ecology Research Award (AERA). They’ve just announced it, so I’m now allowed to boast a bit on Conservation Bytes.

If you’re going to the 50th Anniversary ESA annual conference in Canberra this year ‘Sustaining Biodiversity – the next 50 years‘ (6-10 December), I’ll be giving the AERA Plenary Lecture then. Thanks to the ESA for my selection, the University of Adelaide (The Environment Institute & School of Earth and Environmental Sciences), the South Australian Research and Development Institute, and all my students, post-docs and collaborators for your support. Many thanks also to Prof. Bill Laurance for the nomination!

The AERA blurb from the ESA site follows: Read the rest of this entry »





PhD scholarships in marine plant ecology and conservation

12 05 2010

Two new APAI (Australian Postgraduate Award – Industry) PhD scholarships are available at the University of Adelaide, both in marine ecology and conservation.

Molecular Systematics and Ecology of Marine Macroalgae

Dr. Frederico Gurgel at the University of Adelaide is seeking 2 PhD students interested in working on several aspects of the marine green macroalgal genus Caulerpa. Honour students are also welcome to apply. APAI PhD scholarships are the best-paid scholarships from the Australian Research Council (fees + AU$26,000 p.a. for 3 yrs). Possible co-advisors: Prof. Corey Bradshaw (University of Adelaide/South Australian Research and Development Institute – SARDI), Dr. Jason Tanner (SARDI), and Dr. Marty Deveney (SARDI). External collaborators: Dr. Peter Grewe (CSIRO Marine), Dr. John Runcie (University of Sydney). Starting date: any time.

Integrative approach to the study of Caulerpa taxifolia in Australia: Ecological, Physiology, Phylogeography and DNA barcoding

The students will perform comparative ecological and physiological assays among Australian native and invasive strains of C. taxifolia (and related species) to study their response (e.g., growth, reproduction, photosynthesis, gene expression) to distinct abiotic factors and global climate change scenarios (e.g., pCO2, pH, temperature, light, salinity, nutrients). Students will perform a multi-marker comparative phylogeographic study among 14 invasive (NSW and SA) and 4 native (QLD, NT, WA) populations to determine the origin of introduced populations in temperate Australia. Students will build a dual-marker DNA barcode database of all species of Caulerpa in Australia as a tool to identify morphologically compromised specimens. Additionally, they will perform a molecular-assisted evolutionary (phylogenetic) study of the genus and develop demographic models to predict the fate of Caulerpa populations under different abiotic scenarios. The students will have the option to choose the components of the project they desire.

Desirable skills: 4WD and manual driving, snorkelling, SCUBA diving certification (open water minimum), molecular biology experience.

For more information please contact Dr. Fred Gurgel (e-mail or telephone: +61 8 8222 9291).

Add to FacebookAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to TwitterAdd to TechnoratiAdd to Yahoo BuzzAdd to Newsvine





Fanciful mathematics and ecological fantasy

3 05 2010

© flickr/themadlolscientist

Bear with me here, dear reader – this one’s a bit of a stretch for conservation relevance at first glance, but it is important. Also, it’s one of my own papers so I have the prerogative :-)

As some of you probably know, I dabble quite a bit in population dynamics theory, which basically means examining the mathematics people use to decipher ecological patterns. Why is this important? Well, most models predicting extinction risk, estimating optimal harvest rates, determining minimum viable population size and metapopulation dynamics for species’ persistence rely on good mathematical abstraction to be realistic. Get the maths wrong, and you could end up overharvesting a species (e.g., 99.99 % of fisheries management), underestimating extinction risk from habitat degradation, and getting your predictions wrong about the effects of invasive species. Expressed as an equation itself, (conservation) ecology = mathematics.

A long-standing family of models known as ‘phenomenological’ models (i.e., because they deal with the phenomenon of population size which is an emergent property of the mechanisms of birth, death and immigration) has been used to estimate everything from maximum sustainable yield targets, temporal abundance patterns, wildlife management interventions, extinction risk to epidemiological patterns. The basic form of the model describes the growth response, or the relationship between the population’s rate of change (growth) and its size. The simplest form (known as the Ricker), assumes a linear decline in population growth rate (r) as the number of individuals increases, which basically means that populations can’t grow indefinitely (i.e., they fluctuate around some carrying capacity if unperturbed). Read the rest of this entry »





Classics: Mesopredator Release

17 03 2010

© J. Short

Although popularised by Crooks & Soulé (1999), Soulé et al. (1988) first gave us the term that described how entire ecosystems can become unbalanced by a reduction of a higher trophic-level predator exerting so-called ‘top-down’ control on the abundance of species occupying lower trophic levels.

The idea had theoretical support in ecology (Wright et al. 1994; Litvaitis & Villafuerte 1996), but it was not until Soulé and colleagues described how the decline of dominant predators combines with habitat fragmentation to release top-down pressure on smaller predators, thereby increasing predation rates on prey lower down the trophic web.

Crooks & Soulé (1999) described an example where the decline in coyotes (Canis latrans) in combination with urbanisation-driven habitat fragmentation led to an increase in cat (Felis catus) densities and the subsequent decline in scrub-breeding birds. More recent examples attest to the importance of the mesopredator release phenomenon: Myers et al. (2007) described how the decline in large coastal shark species has allowed mesopredator cownose rays (Rhinoptera bonasus) to increase, leading to a reduction in commercially important shellfish densities; and Johnson et al. (2007) showed how dingoes (Canis lupus dingo) in Australia suppress populations of exotic predators such as cats and foxes, leading to more locally abundant populations of native marsupials (see previous post).

Conservation biologists have benefited from this knowledge because we’ve realised that top-order predators affect far more than their immediate prey. These examples really hit home how a fully functional community is required for ecosystem stability, so we should strive to preserve complete complements of communities, not just our favourite species.

CJA Bradshaw

Add to FacebookAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to TwitterAdd to TechnoratiAdd to Yahoo BuzzAdd to Newsvine





Global pollinator declines

11 03 2010

Mention anything about ecosystem services – those ecological functions arising from the interactions between species that provide some benefit (source of food/clean water, health, etc.) to humanity1 – and one of the most cited examples is pollination.

It’s really a no-brainer, hence its popularity as an example. Pollinators (mainly insects, but birds, bats and other assorted species too) don’t exist to pollinate plants; rather, their principal source of food acquisition happens to spread around the gametes of the plants they regularly visit. Evolution has favoured the dependence of species in such ways because the mutualism benefits all involved, and in some cases, this dependence has become obligate. So when the habitats that pollinators need to survive are reduced or destroyed, inevitably their population sizes decline and the plants on which they feed lose their main sources of gene-spreading.

So what? Well, about 80 % of all wild plant species require insect pollinators for fruit and seed set, and about 75 % of all human crops require pollination by insects (mostly bees). So it’s pretty frightening to consider that although our global population is at 6.8 billion and growing rapidly, our main food pollinators (bees) are declining globally (see also previous post on bee declines). Indeed, domestic honey bee stocks have declined in the USA by 59 % since 1947 and in Europe by 25 % since 1985. Scared yet?

Another thing people don’t tend to get is that a bee cannot live on rapeseed alone. Most pollinators require intact forests to complete many of their other life history requirements (breeding, shelter, etc.) and merely forage occasionally in crop lands. Cut down all the adjacent bush, and your crops will suffer accordingly.

These, and other titbits to keep you awake at night and worry about what your grandchildren might eat are highlighted in a recent review in Trends in Ecology and Evolution by Potts and colleagues entitled Global pollinator declines: trends, impacts and drivers.

What’s driving all this loss? Several things, but it’s mainly due to ‘land-use change’ (a bullshit word people use generally to mean habitat loss, fragmentation and degradation). However, invasive species competition, pathogens and parasites, and climate change (and the synergies amongst all of these) are all contributing.

It always amazes me when people ask me why biodiversity is important. Despite the overwhelming knowledge we’ve accumulated about how functioning ecosystems make the planet liveable, despite it just being plainly stupid to think that humans are somehow removed from normal biological processes, and even with such in-your-face examples of global pollinator declines and the real, extremely worrying implication for food supplies, many people just don’t seem to get it. Every tree you cut down, every molecule of carbon dioxide you release, every drop of water you waste will punish you and your family directly for generations to come. How much more self-evident can you get?

Humanity seems to have a very poorly developed sense of self-preservation.

CJA Bradshaw

1It’s amazingly arrogant and anthropocentric to think of anything in ecosystems as ‘providing benefits to humanity’. After all, we’re just another species in a complex array of species within ecosystems – we just happen to be one of the numerically dominant ones, excel at ecosystem ‘engineering’ and as far as we know, are the only (semi-)sentient of the biologicals. Although the concept of ecosystem services is, I think, an essential abstraction to place emphasis on the importance of biodiversity conservation to the biodiversity ignorant, it does rub me a little the wrong way. It’s almost ascribing some sort of illogical religious perspective that the Earth was placed in its current form for our eventual benefit. We might be a fairly new species in geological time scales, but don’t think of ecosystems as mere provisions for our well-being.

ResearchBlogging.orgPotts, S., Biesmeijer, J., Kremen, C., Neumann, P., Schweiger, O., & Kunin, W. (2010). Global pollinator declines: trends, impacts and drivers Trends in Ecology & Evolution DOI: 10.1016/j.tree.2010.01.007

Add to FacebookAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to TwitterAdd to TechnoratiAdd to Yahoo BuzzAdd to Newsvine





Vodcast on killing for conservation

24 02 2010

The inaugural issue of Methods in Ecology and Evolution came out today (see first issue editorial) and I am very pleased not only that our paper (Spatially explicit spreadsheet modelling for optimizing the efficiency of reducing invasive animal density) made it into the the paper line-up (see previous ConservationBytes.com post on the paper here), we also managed to score the journal’s cover image (buffalo image shown right: Asian swamp buffalo Bubalus bubalis introduced to Australia in the early 19th Century now populate much of the tropical north and cause severe environmental disturbances to savanna and wetland ecosystems. Despite a broad-scale cull of hundreds of thousands of free-ranging buffalo occurring in the 1980s and 1990s to eradicate brucellosis and tuberculosis, the population is recovering and continuing to threaten protected areas such as Kakadu National Park. A small wild harvest of several thousand buffalo occurs each year in Arnhem Land where mustering is aided by helicopters and on-ground vehicles. The buffalo pictured are housed in temporary holding pens and then shipped for live export. Photo credit: Jesse Northfield).

I also had the opportunity to chat with Journal Coordinator, Graziella Iossa, via Skype about the paper, and they have put up a YouTube vodcast of the interview itself. You can also check it out here.

Summary: Corey Bradshaw answers what is the main idea behind his work with co-authors, “Spatially explicit spreadsheet modelling for optimising the efficiency of reducing invasive animal density”. Further, he explains how their model advances methodology in ecology and evolution and finally shows how it could be applied by wildlife manager and practitioners with basic knowledge of computer models. Their Excel-spreadsheet ‘Spatio-Temporal Animal Reduction’ (S.T.A.R.) model is designed specifically to optimise the culling strategies for feral pigs, buffalo and horses in Kakadu National Park (northern Australia), but Corey explains how their aim was to make it easy enough for anyone to use and modify it so that it could be applied to any invasive species anywhere.

Congratulations to Editor-in-Chief Rob Freckleton, Graziella and the Associate Editors for a great first issue. Other titles include:

Keep them coming!

CJA Bradshaw

Add to FacebookAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to TwitterAdd to TechnoratiAdd to Yahoo BuzzAdd to Newsvine





Inbreeding bad for invasives too

18 02 2010

I just came across this little gem of a paper in Molecular Ecology (not, by any stretch, a common forum for biodiversity conservation-related papers). It’s another one of those wonderful little experimental manipulation studies I love so much (see previous examples here and here).

I’ve written a lot before about the loss of genetic diversity as a contributing factor to extinction risk, via things like Allee effects and inbreeding depression. I’ve also posted blurbs about our work and that of others on what makes particular species prone to become extinct or invasive (i.e., the two sides of the same evolutionary coin). Now Crawford and Whitney bring these two themes together in their paper entitled Population genetic diversity influences colonization success.

Yes, the evolved traits of a particular species will set it up either to do well or very badly under rapid environmental change, and invasive species tend to be those with rapid generation times, defence mechanisms, heightened dispersal capacity and rapid growth. However, such traits generally only predict a small amount in the variation in invasion success – the other being of course propagule pressure (a composite measure of the number of individuals of a non-native species [propagule size] introduced to a novel environment and the number of introduction events [propagule number] into the new host environment).

But, that’s not all. It turns out that just as reduced genetic diversity enhances a threatened species’ risk of extinction, so too does it reduce the ‘invasiveness’ of a weed. Using experimentally manipulated populations of the weedy herb Arabidopsis thaliana (mouse-ear cress; see if you get the joke), Crawford & Whitney measured greater population-level seedling emergence rates, biomass production, flowering duration and reproduction in high-diversity populations compared to lower-diversity ones. Maintain a high genetic diversity and your invasive species has a much higher potential to colonise a novel environment and spread throughout it.

Of course, this is related to propagule pressure because the more individuals that invade/are introduced the more times, the higher the likelihood that different genomes will be introduced as well. This is extremely important from a management perspective because it means that well-mixed (outbred) samples of invasive species probably can do a lot more damage to native biodiversity than a few, genetically similar individuals alone. Indeed, most introductions probably don’t result in a successful invasion mainly because they don’t have the genetic diversity to get over the hump of inbreeding depression in the first place.

The higher genetic (and therefore, phenotypic) variation in your pool of introduced individuals, the great the chance that at least a few will survive and proliferate. This is also a good bit of extra proof for our proposal that invasion and extinction are two sides of the same evolutionary coin.

CJA Bradshaw

ResearchBlogging.orgCrawford, K., & Whitney, K. (2010). Population genetic diversity influences colonization success Molecular Ecology DOI: 10.1111/j.1365-294X.2010.04550.x

Bradshaw, C., Giam, X., Tan, H., Brook, B., & Sodhi, N. (2008). Threat or invasive status in legumes is related to opposite extremes of the same ecological and life-history attributes Journal of Ecology, 96, 869-883 DOI: 10.1111/j.1365-2745.2008.01408.x

Add to FacebookAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to TwitterAdd to TechnoratiAdd to Yahoo BuzzAdd to Newsvine





February Issue of Conservation Letters

13 02 2010




Salamander Longshanks – breed them out

3 02 2010

© M. Dawson

Patrick McGoohan in his role as the less-than-sentimental King Edward ‘Longshanks’ in the 1995 production of ‘Braveheart’ said it best in his references to the invocation of ius primæ noctis:

If we can’t get them out, we’ll breed them out

What a charmer.

Dabbling in molecular ecology myself over the past few years with some gel-jockey types (e.g., Dick Frankham [author of Introduction to Conservation Genetics], Melanie Lancaster, Paul Sunnucks, Yuji Isagi inter alios), I’m quite fascinated by the application of good molecular techniques in conservation biology. So when I came across the paper by Fitzpatrick and colleagues entitled Rapid spread of invasive genes into a threatened native species in PNAS, I was quite pleased.

When people usually think about invasive species, they tend to think ‘predator eating naïve native prey’ or ‘weed outcompeting native plant’. These are all big problems (e.g., think feral cats in Australia or knapweed in the USA), but what people probably don’t think about is the insidious concept of ‘genomic extinction’. This is essentially a congener invasive species breeding with a native one, thus ‘diluting’ the native’s genome until it no longer resembles its former self. A veritable case of ‘breeding them out’.

Who cares if at least some of the original genome remains? Some would argue that ‘biodiversity’ should be measured in terms of genetic diversity, not just species richness (I tend to agree), so any loss of genes is a loss of biodiversity. Perhaps more practically, hybridisation can lead to reduced fitness, like we observed in hybridised fur seals on Macquarie Island.

Fitzpatrick and colleagues measured the introgression of alleles from the deliberately introduced barred tiger salamander (Ambystoma tigrinum mavortium) into threatened California tiger salamanders (A. californiense) out from the initial introduction site. While most invasive alleles neatly stopped appearing in sampled salamanders not far from the introduction site, three invasive alleles persisted up to 100 km from the introduction site. Not only was the distance remarkable for such a small, non-dispersing beastie, the rate of introgression was much faster than would be expected by chance (60 years), suggesting selection rather than passive genetic drift. Almost none of the native alleles persisted in the face of the three super-aggressive invasive alleles.

The authors claim that the effects on native salamander fitness are complex and it would probably be premature to claim that the introgression is contributing to their threatened status, but they do raise an important management conundrum. If species identification rests on the characterisation of a specific genome, then none of the native salamanders would qualify for protection under the USA’s Endangered Species Act. They believe then that so-called ‘genetic purity’ is an impractical conservation goal, but it can be used to shield remaining ‘mostly native’ populations from further introgression.

Nice study.

CJA Bradshaw

ResearchBlogging.orgFitzpatrick, B., Johnson, J., Kump, D., Smith, J., Voss, S., & Shaffer, H. (2010). Rapid spread of invasive genes into a threatened native species Proceedings of the National Academy of Sciences DOI: 10.1073/pnas.0911802107

Lancaster, M., Bradshaw, C.J.A., Goldsworthy, S.D., & Sunnucks, P. (2007). Lower reproductive success in hybrid fur seal males indicates fitness costs to hybridization Molecular Ecology, 16 (15), 3187-3197 DOI: 10.1111/j.1365-294X.2007.03339.x

Add to FacebookAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to TwitterAdd to TechnoratiAdd to Yahoo BuzzAdd to Newsvine





Computer-assisted killing for conservation

12 01 2010

Many non-Australians might not know it, but Australia is overrun with feral vertebrates (not to mention weeds and invertebrates). We have millions of pigs, dogs, camels, goats, buffalo, deer, rabbits, cats, foxes and toads (to name a few). In a continent that separated from Gondwana about 80 million years ago, this allowed a fairly unique biota to evolve, such that when Aboriginals and later, Europeans, started introducing all these non-native species, it quickly became an ecological disaster. One of my first posts here on ConservationBytes.com was in fact about feral animals. Since then, I’ve written quite a bit on invasive species, especially with respect to mammal declines (see Few people, many threats – Australia’s biodiversity shame, Shocking continued loss of Australian mammals, Can we solve Australia’s mammal extinction crisis?).

So you can imagine that we do try to find the best ways to reduce the damage these species cause; unfortunately, we tend to waste a lot of money because density reduction culling programmes aren’t usually done with much forethought, organisation or associated research. A case in point – swamp buffalo were killed in vast numbers in northern Australia in the 1980s and 1990s, but now they’re back with a vengeance.

Enter S.T.A.R. – the clumsily named ‘Spatio-Temporal Animal Reduction’ [model] that we’ve just published in Methods in Ecology and Evolution (title: Spatially explicit spreadsheet modelling for optimising the efficiency of reducing invasive animal density by CR McMahon and colleagues).

This little Excel-based spreadsheet model is designed specifically to optimise the culling strategies for feral pigs, buffalo and horses in Kakadu National Park (northern Australia), but our aim was to make it easy enough to use and modify so that it could be applied to any invasive species anywhere (ok, admittedly it would work best for macro-vertebrates).

The application works on a grid of habitat types, each with their own carrying capacities for each species. We then assume some fairly basic density-feedback population models and allow animals to move among cells. We then hit them virtually with a proportional culling rate (which includes a hunting-efficiency feedback), and estimate the costs associated with each level of kill. The final outputs give density maps and graphs of the population trajectory.

We’ve added a lot of little features to maximise flexibility, including adjusting carrying capacities, movement rates, operating costs and overheads, and proportional harvest rates. The user can also get some basic sensitivity analyses done, or do district-specific culls. Finally, we’ve included three optimisation routines that estimate the best allocation of killing effort, for both maximising density reduction or working to a specific budget, and within a spatial or non-spatial context.

Our hope is that wildlife managers responsible for safeguarding the biodiversity of places like Kakadu National Park actually use this tool to maximise their efficiency. Kakadu has a particularly nasty set of invasive species, so it’s important those in charge get it right. So far, they haven’t been doing too well.

You can download the Excel program itself here (click here for the raw VBA code), and the User Manual is available here. Happy virtual killing!

CJA Bradshaw

P.S. If you’re concerned about animal welfare issues associated with all this, I invite you to read one of our recent papers on the subject: Convergence of culture, ecology and ethics: management of feral swamp buffalo in northern Australia.

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl

ResearchBlogging.orgC.R. McMahon, B.W. Brook,, N. Collier, & C.J.A. Bradshaw (2010). Spatially explicit spreadsheet modelling for optimising the efficiency of reducing invasive animal density Methods in Ecology and Evolution : 10.1111/j.2041-210X.2009.00002.x

Albrecht, G., McMahon, C., Bowman, D., & Bradshaw, C. (2009). Convergence of Culture, Ecology, and Ethics: Management of Feral Swamp Buffalo in Northern Australia Journal of Agricultural and Environmental Ethics, 22 (4), 361-378 DOI: 10.1007/s10806-009-9158-5

Bradshaw, C., Field, I., Bowman, D., Haynes, C., & Brook, B. (2007). Current and future threats from non-indigenous animal species in northern Australia: a spotlight on World Heritage Area Kakadu National Park Wildlife Research, 34 (6) DOI: 10.1071/WR06056





Conservation Biology for All

26 12 2009

A new book that I’m proud to have had a hand in writing is just about to come out with Oxford University Press called Conservation Biology for All. Edited by the venerable Conservation Scholars, Professors Navjot Sodhi (National University of Singapore) and Paul Ehrlich (Stanford University), it’s a powerhouse of some of the world’s leaders in conservation science and application.

The book strives to “…provide cutting-edge but basic conservation science to a global readership”. In short, it’s written to bring the forefront of conservation science to the general public, with OUP promising to make it freely available online within about a year from its release in early 2010 (or so the rumour goes). The main idea here is that those in most need of such a book – the conservationists in developing nations – can access the wealth of information therein without having to sacrifice the village cow to buy it.

I won’t go into any great detail about the book’s contents (mainly because I have yet to receive my own copy and read most of the chapters!), but I have perused early versions of Kevin Gaston‘s excellent chapter on biodiversity, and Tom Brook‘s overview of conservation planning and prioritisation. Our chapter (Chapter 16 by Barry Brook and me), is an overview of statistical and modelling philosophy and application with emphasis on conservation mathematics. It’s by no means a complete treatment, but it’s something we want to develop further down the track. I do hope many people find it useful.

I’ve reproduced the chapter title line-up below, with links to each of the authors websites.

  1. Conservation Biology: Past and Present (C. Meine)
  2. Biodiversity (K. Gaston)
  3. Ecosystem Functions and Services (C. Sekercioglu)
  4. Habitat Destruction: Death of a Thousand Cuts (W. Laurance)
  5. Habitat Fragmentation and Landscape Change (A. Bennett & D. Saunders)
  6. Overharvesting (C. Peres)
  7. Invasive Species (D. Simberloff)
  8. Climate Change (T. Lovejoy)
  9. Fire and Biodiversity (D. Bowman & B. Murphy)
  10. Extinctions and the Practice of Preventing Them (S. Pimm & C. Jenkins)
  11. Conservation Planning and Priorities (T. Brooks)
  12. Endangered Species Management: The US Experience (D. Wilcove)
  13. Conservation in Human-Modified Landscapes (L.P. Koh & T. Gardner)
  14. The Roles of People in Conservation (A. Claus, K. Chan & T. Satterfield)
  15. From Conservation Theory to Practice: Crossing the Divide (M. Rao & J. Ginsberg)
  16. The Conservation Biologist’s Toolbox – Principles for the Design and Analysis of Conservation Studies (C. Bradshaw & B. Brook)

As you can see, it’s a pretty impressive collection of conservation stars and hard-hitting topics. Can’t wait to get my own copy! I will probably blog individual chapters down the track, so stay tuned.

CJA Bradshaw

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl





Scoping the future threats and solutions to biodiversity conservation

4 12 2009

Way back in 1989, Jared Diamond defined the ‘evil quartet’ of habitat destruction, over-exploitation, introduced species and extinction cascades as the principal drivers of modern extinctions. I think we could easily update this to the ‘evil quintet’ that includes climate change, and I would even go so far as to add extinction synergies as a the sixth member of the ‘evil sextet’.

But the future could hold quite a few more latent threats to biodiversity, and a corresponding number of potential solutions to its degradation. That’s why Bill Sutherland of Cambridge University recently got together with some other well-known scientists and technology leaders to do a ‘horizon scanning’ exercise to define what these threats and solutions might be in the immediate future. It’s an interesting, eclectic and somewhat enigmatic list, so I thought I’d summarise it here. The paper is entitled A horizon scan of global conservation issues for 2010 and was recently published online in Trends in Ecology and Evolution.

In no particular order or relative rank, Sutherland and colleagues list the following 15 ‘issues’ that I’ve broadly divided into ‘Emerging Threats’ and ‘Potential Solutions’:

Emerging Threats

  1. Microplastic pollution – The massive increase in plastics found in the world’s waterways and oceans really doesn’t have much focus right now in conservation research, but it should. We really don’t know how much we’re potentially threatening species with this source of pollution.
  2. Nanosilver in wastewater – The ubiquity of antimicrobial silver oxide or ions in products these days needs careful consideration for what the waste might be doing to our microbial communities that keep ecosystems alive and functioning.
  3. Stratospheric aerosols – A simultaneous solution and threat. Creating what would in effect be an artificial global cooling by injecting particles like sulphate aerosols into the stratosphere might work to cool the planet down somewhat. However, it would not reduce carbon dioxide, ocean acidification or other greenhouse gas-related changes. This strikes me as a potential for serious mucking up of the global climate and only a band-aid solution to the real problem.
  4. Deoxygenation of the oceans – Very scary. Ironically today I was listening to a talk by Martin Kennedy on the deep-time past of ocean hypoxia and he suggests we’re well on our way to a situation where our shelf waters could essentially become too anoxic for marine life to persist. It’s happened before, and rapid climate change makes the prospect plausible within less than a century. And you thought acidification was scary.
  5. Changes in denitrifying bacteria – Just like we’re changing the carbon cycle, we’re buggering up the nitrogen cycle as well. Changing our water bodies to nitrogen sources rather than sinks could fundamentally change marine ecosystems for the worse.
  6. High-latitude volcanism – One of these horrible positive feedback ideas. Reducing high-latitude ice cover exposes all these slumbering volcanoes that once ‘released’, start increasing atmospheric gas concentrations and contributing to faster ice melt and sea level rise.
  7. Trans-Arctic dispersal and colonisation – Warming polar seas and less ice mean fewer barriers to species movements. Expect Arctic ecosystems to be a hotbed of invasion, regime shifts and community reshuffling as a result.
  8. Invasive Indo-Pacific lionfish – Not one I would have focussed on, but interesting. These spiny, venomous fish like to eat a lot of other species, and so represent a potentially important invasive species in the marine realm.
  9. REDD and non-forested ecosystems – Heralded as a great potential coup for forest preservation and climate change mitigation, focussing on maintaining forests for their carbon sequestration value might divert pressure toward non-forested habitats and ironically, threaten a whole new sphere of species.
  10. International land acquisition – Global financial crises and dwindling food supplies mean that governments are acquiring more and more huge tracts of land for agricultural development. While this might solve some immediate issues, it could potentially threaten a lot more undeveloped land in the long run, putting even more pressure on habitats.

Potential Solutions

  1. Synthetic meat – Ever thought about eating a sausage grown in a vat rather than cut from a dead pig? It could become the norm and a way of reducing the huge pressure on terrestrial and aquatic systems for the production of livestock and fish for human protein provision.
  2. Artificial life – Both a risk and a potential solution. While I’ve commented before on the pointlessness of cloning technology for conservation, the ability to create genomes and reinvigorate species on the brink is an exciting prospect. It’s also frightening as hell because we don’t know how all these custom-made genomes might react and transform naturally evolved ones.
  3. Biochar – Burn organic material (e.g., plant matter) in the absence of oxygen, you get biochar. This essentially sequesters a lot of carbon that can then be put underground. The upshot is that agricultural yields can also increase. Would there be a trade-off though between land available for biochar sequestration and natural habitats?
  4. Mobile-sensing technology – Not so much a solution per se, but the rapid acceleration of remote technology will make our ability to measure and predict the subtleties of ecosystem and climate change much more precise. A lot more work and application required here.
  5. Assisted colonisationI’ve blogged about this before. With such rapid shifts in climate, we might be obliged to move species around so that they can keep up with rapidly changing conditions. Many pros and cons here, not least of which is exacerbating the invasive species problems around the globe.

Certainly some interesting ideas here and worth a thought or two. I wonder if the discipline of ‘conservation biology’ might even exist in 50-100 years – we might all end up being climate or agricultural engineers with a focus on biodiversity-friendly technology. Who knows?

CJA Bradshaw

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl

ResearchBlogging.orgSutherland, W., Clout, M., Côté, I., Daszak, P., Depledge, M., Fellman, L., Fleishman, E., Garthwaite, R., Gibbons, D., & De Lurio, J. (2009). A horizon scan of global conservation issues for 2010 Trends in Ecology & Evolution DOI: 10.1016/j.tree.2009.10.003





Value of a good enemy

25 10 2009

alienpredatorI love these sorts of experiments. Ecology (and considering conservation ecology a special subset of the larger discipline) is a messy business, mainly because ecosystems are complex, non-linear, emergent, interactive, stochastic and meta-stable entities that are just plain difficult to manipulate experimentally. Therefore, making inference of complex ecological processes tends to be enhanced when the simplest components are isolated.

Enter the ‘mini-ecosystem-in-a-box’ approach to ecological research. I’ve blogged before about some clever experiments to examine the role of connectivity among populations in mitigating (or failing to mitigate) extinction risk, and alluded to others indicating how harvest reserves work to maximise population persistence. This latest microcosm experiment is another little gem and has huge implications for conservation.

A fairly long-standing controversy in conservation biology, and in invasive species biology in particular, is whether intact ecosystems are in any way more ‘resilient’ to invasion by alien species (the latter most often being deliberately or inadvertently introduced by humans – think of Australia’s appalling feral species problems; e.g., buffalo, foxes and cats, weeds). Many believe by default that more ‘pristine’ (i.e., less disturbed by humans) communities will naturally provide more ecological checks against invasives because there are more competitors, more specialists and more predators. However, considering the ubiquity of invasives around the world, this assumption has been challenged vehemently.

The paper I’m highlighting today uses the microcosm experimental approach to show how native predators, when abundant, can reduce the severity of an invasion. Using a system of two mosquito species (one ‘native’ – what’s ‘native’ in a microcosm? [another subject] – and one ‘invasive’) and a native midge predator, Juliano and colleagues demonstrate in their paper Your worst enemy could be your best friend: predator contributions to invasion resistance and persistence of natives that predators are something you want to keep around.

In short, they found little evidence of direct competition between the two mosquitoes in terms of abundance when placed together without predators, but when the midges were added, the persistence of the invasive mosquito was reduced substantially. Of course, the midge predators did do their share of damage on the native mosquitoes in terms of reducing the latter’s abundance, but through a type of competitive release from their invasive counterparts, the midges’ reduction of the invasive species left the native mosquito free to develop faster (i.e., more per capita resources).

Such a seemingly academic result has huge conservation implications. In most systems, predators are some of the largest and slowest-reproducing species, so they are characteristically the first to feel the hammer of human damage. From bears to sharks, and tigers to wolves, big, charismatic predators are on the wane worldwide. Juliano and colleagues’ nice experimental work with insects reminds us that keeping functioning native ecosystems intact from all trophic perspectives is imperative.

CJA Bradshaw

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl

This post was chosen as an Editor's Selection for ResearchBlogging.org

ResearchBlogging.orgJuliano, S., Lounibos, L., Nishimura, N., & Greene, K. (2009). Your worst enemy could be your best friend: predator contributions to invasion resistance and persistence of natives Oecologia DOI: 10.1007/s00442-009-1475-x





Life and death on Earth: the Cronus hypothesis

13 10 2009
Cronus

Cronus

Bit of a strange one for you today, but here’s a post I hope you’ll enjoy.

My colleague, Barry Brook, and I recently published a paper in the very new and perhaps controversial online journal , the Journal of Cosmology. Cosmology? According to the journal, ‘cosmology’ is:

“the study and understanding of existence in its totality, encompassing the infinite and eternal, and the origins and evolution of the cosmos, galaxies, stars, planets, earth, life, woman and man”.

The journal publishes papers dealing with ‘cosmology’ and is a vehicle for those who wish to publish on subjects devoted to the study of existence in its totality.

Ok. Quite an aim.

Our paper is part of the November (second ever) issue of the journal entitled Asteroids, Meteors, Comets, Climate and Mass Extinctions, and because we were the first to submit, we managed to secure the first paper in the issue.

Our paper, entitled The Cronus hypothesis – extinction as a necessary and dynamic balance to evolutionary diversification, introduces a new idea in the quest to find that perfect analogy for understanding the mechanisms dictating how life on our planet has waxed and waned over the billions of years since it first appeared.

Gaia

Gaia

In the 1960s, James Lovelock conceived the novel idea of Gaia – that the Earth functions like a single, self-regulating organism where life itself interacts with the physical environment to maintain conditions favourable for life (Gaia was the ancient Greeks’ Earth mother goddess). Embraced, contested, denounced and recently re-invigorated, the idea has evolved substantially since it first appeared. More recently (this year, in fact), Peter Ward countered the Gaia hypothesis with his own Greek metaphor – the Medea hypothesis. Essentially this view holds that life instead ‘seeks’ to destroy itself in an anti-Gaia manner (Medea was the siblicidal wife of Jason of the Argonauts). Ward described his Medea hypothesis as “Gaia’s evil twin”.

One can marvel at the incredible diversity of life on Earth (e.g., conservatively, > 4 million protists, 16600 protozoa, 75000-300000 helminth parasites, 1.5 million fungi, 320000 plants, 4-6 million arthropods, > 6500 amphibians, 10000 birds and > 5000 mammals) and wonder that there might be something in the ‘life makes it easier for life’ idea underlying Gaia. However, when one considers that over 99 % of all species that have ever existed are today extinct, then a Medea perspective might dominate.

Medea

Medea

Enter Cronus. Here we posit a new way of looking at the tumultuous history of life and death on Earth that effectively relegates Gaia and Medea to opposite ends of a spectrum. Cronus (patricidal son of Gaia overthrown by his own son, Zeus, and banished to Hades) treats speciation and extinction as birth and death in a ‘metapopulation’ of species assemblages split into biogeographic realms. Catastrophic extinction events can be brought about via species engineering their surroundings by passively modifying the delicate balance of oxygen, carbon dioxide and methane – indeed, humans might be the next species to fall victim to our own Medean tendencies. But extinction opens up new niches that eventually elicit speciation, and under conditions of relative environmental stability, specialists evolve because they are (at least temporarily) competitive under those conditions. When conditions change again, extinction ensues because not all can adapt quickly enough. Just as all individuals born in a population must eventually die, extinction is a necessary termination.

We think the Cronus metaphor has a lot of advantages over Gaia and Medea. The notion of a community of species as a population of selfish individuals retains the Darwinian view of contestation; self-regulation in Cronus occurs naturally as a result of extinction modifying the course of future evolution. Cronus also makes existing mathematical tools developed for metapopulation theory amenable to broader lines of inquiry.

For example, species as individuals with particular ‘mortality’ (extinction) rates, and lineages with particular ‘birth’ (speciation) rates, could interact and disperse among ‘habitats’ (biogeographical realms). ‘Density’ feedback could be represented as competitive exclusion or symbioses. As species dwindle, feedbacks such as reduced community resilience that further exacerbate extinction risk (Medea-like phase), and stochastic fluctuation around a ‘carrying capacity’ (niche saturation) arising when environmental conditions are relatively stable is the Gaia-like phase. Our Cronus framework is also scale-invariant – it could be applied to microbial diversity on another organism right up to inter-planetary exchange of life (panspermia).

What’s the relevance to conservation? We’re struggling to prevent extinction, so understanding how it works is an essential first step. Without the realisation that extinction is necessary (albeit, at rates preferably slower than they are currently), we cannot properly implement conservation triage, i.e., where do we invest in conservation and why?

We had fun with this, and I hope you enjoy it too.

CJA Bradshaw

ResearchBlogging.orgBradshaw, C.J.A., & Brook, B.W. (2009). The Cronus Hypothesis – extinction as a necessary and dynamic balance to evolutionary diversification Journal of Cosmology, 2, 201-209 Other: http://journalofcosmology.com/Extinction100.html

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl





Coming to grips with the buffalo problem

7 09 2009

Clive McMahon (left) & colleaguesA good friend and colleague of mine, Dr. Clive McMahon, is visiting Adelaide for the next few weeks from Darwin. We’re attacking a few overdue manuscripts and sampling a few of Adelaide’s better drops of value-added grape juice, so I asked him to do a guest post on ConservationBytes.com about his work. So here it is, something perhaps even few Australians know much about, let alone overseas folks. If you can recall that very strange scene in the film Crocodile Dundee where the old croc hunter casts a gestured spell over a horned beast, then you’ll probably appreciate this post.

Yes, there are plenty of them in northern Australia

Invasive and feral species can be important drivers of biodiversity loss. Australia, like many other isolated islands has developed an ancient, unique and diverse ecosystem. This unique ecosystem has been under extreme pressure ever since humans arrived around 40000-60000 years ago. One of the more damaging and economically important introduced species in Australia is the Asian swamp buffalo (Bubalus bubalis). Ironically, swamp buffalo are listed as Endangered by the IUCN, and current estimates suggest that there are probably less than 4000 in their native habitats in Asia.

© B. Salu, Kakadu National Park

© B. Salau, Kakadu National Park

The first 16 buffalo were introduced to Australia in 1826 on Melville Island, and then to the mainland at Cobourg Peninsula a year later from Kupang (now West Timor, Indonesia). Another 18 buffalo were obtained from Kisar Island (northeast of modern Timor-Leste) and introduced to the Cobourg. In 1843, another 49 were introduced. When the first Cobourg settlement was abandoned in 1849, all the buffalo were released, and the population spread rapidly throughout the Northern Territory. Over the next 65 years, numbers and distribution increased to an estimated 350000 in the 1960s and 1970s and densities exceeded 25 km-2 in ‘prime’ habitat. However, the population was severely reduced during the 1980s and 1990s in parts of its range under the Brucellosis-Tuberculosis Eradication Campaign (BTEC). Although largely successful in eradicating buffalo from pastoral lands in the short term, there was no ongoing broad-scale management of numbers and the present-day population of free-ranging buffalo has recovered to former densities in some areas.

© C. Speed

© C. Speed

Buffalo were then and still are major problem in Australia due mainly to the environmental damage they cause, such as saltwater intrusion of wetlands and trampling of sensitive habitats, their potential threat to Australia’s livestock industry as hosts for disease, and the danger they pose to human safety. Given these ecological, economic and social impacts, there is an urgent need to manage buffalo numbers.

An important step to inform management of introduced and invasive species is to determine the history of introduction and quantify the rate of spread from introduction sites. Contemporary genetic techniques in conjunction with demographic and life history information are useful tools for understanding the dynamics, population structure, biology and colonisation dynamics of plants and animals, including invasive species such as buffalo.

We are currently in the final stages of providing the first detailed analysis of the buffalo population structure (demographic and genetic) to (1) establish the rate and most probable history of spread using detailed genetic information sampled from 8 sub-populations, (2) quantify the genetic distance and mixing rates between populations and (3) describe the age structure and therefore the demographic performance of this very successful invasive species.

Firstly to get an idea of genetic structure and relatedness, we collected a total of 430 small skin biopsies from buffalo across the Northern Territory, representing eight geographically distinct populations. To determine what has made the buffalo such a successful invader it is important to know the survival and breeding performance; we also constructed seven life tables based on culled samples at different densities and in different environments to work out what are the critical components of the population – i.e., where management intervention would be most successful.

As expected from a bottlenecked population, genetic variation is low compared to the that found in swamp buffalo from India and South East Asia. Despite this reduced genetic variation, the Australian population has thrived and spread outwards from introduction sites and into culled sites at high rates over the last 160 years (covering ~ 224 000 km2 in that time).

Although buffalo in Australia experienced two major periods of population reduction since their introduction, a small proportion (estimated at ~ 20 %) escaped the BTEC reduction in the eastern part of its north Australian range. BTEC did not operate with uniformity across the entire range of buffalo, concentrating its destocking efforts in a general area from the western coast of the Northern Territory to west of the Mann River in Arnhem Land, and south roughly to Kakadu National Park’s southern border. Coincidently and not surprisingly, it is in this area that we observe most migration activity.

The subpopulation structure detected here suggests that each population, while connected over generational time scales, generally remains in its immediate vicinity over the course of management-tractable periods. Therefore, management aimed at protecting Australia’s lucrative livestock industry trading under Australia’s disease-free status will benefit directly from this knowledge. For example, the localised introduction and subsequent rapid detection of disease could be efficiently managed from local culls because short-term movements of long-distance are less likely. Our results showcase how management of animals for disease control can be effectively informed via genetic studies and so avoid the need for expensive broad-scale intervention.

Our analyses of the age structure of buffalo reveals that buffalo have the capacity to recover swiftly after control because of high survival and fertility rates. Survival in the juvenile age classes was consistently the most important modifier of population growth. In populations where juvenile animals are harvested annually, fertility determined rebound potential. Thus, management aimed at long-term control of densities should focus primarily on the sustained culling of adult females and their offspring.

Given that numbers of buffalo are increasing and that buffalo are extremely well-adapted to the monsoonal tropics (unlike cattle, buffalo can maintain body condition and positive growth during times of food shortages), they are vulnerable to extended periods of harsh conditions. Climate change predictions herald increasing rainfall in the region, thereby potentially reducing the pressure on juvenile survival. As such, buffalo population growth could conceivably increase, making future management much more difficult. In essence, we need a large, evidence-based density reduction programme in place soon to prevent the worst ecological damage to Australia’s sensitive and unique ecosystems.

Check back here for announcements of upcoming publications arising from our work.

Clive McMahon & CJA Bradshaw

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl





Can we solve Australia’s mammal extinction crisis?

3 09 2009

© F. O'Connor

© F. O'Connor

This ‘In DepthScience Opinion piece from the ABC couldn’t have come at a better time. Written by Ian Gordon of the CSIRO, this opinion piece was written off the back of the special session on mammalian extinctions held at the recent International Congress of Ecology in Brisbane. Three previous ConservationBytes.com blogs in August (here, here and here) were devoted to specific talks at the Congress, including one about John Woinarksi’s gloomy tale of dwindling mammal populations in the Top End (which is especially frightening considering its also going on in our so-called ‘protected’ areas such as Kakadu, Litchfield and Garig Gunak Barlu National Parks!).

So, I recommend you have a read of my blog post on the shocking continued loss of Australian mammals, then read Ian’s piece copied below. Bottom lines – stop burning the shit out of our forests and encourage dingo population recovery and expansion.

Australia leads the world in mammal extinctions.

Over the last two hundred years 22 mammal species have become extinct, and over 100 are now on the threatened and endangered species list, compiled as part of the federal government’s Environment Protection and Biodiversity Conservation Act.

Evidence suggests Australia is on the cusp of another wave of mammal extinctions with a reduction in the abundance of some species and alarmingly, their range.

This is undoubtedly one of the major biodiversity conservation issues affecting Australia. It’s crucial we focus on the management solutions required to stop these species falling into extinction.

A South American success story

Working as a zoologist has allowed me to be involved in projects across the globe, looking at species at risk of extinction due to over-exploitation by humans.

Earlier this year I edited a book on the South American vicuña‘s comeback from the brink of extinction. Once abundant in the Andes, this wild relative of the llama suffered a sharp population drop in the 1960s due to international demand for its fleece.

An international moratorium on the sale of vicuña fleece in 1969 saw populations recover enough by 1987 for Andean communities to be able to harvest the fibre in a sustainable way. Population numbers of vicuña have remained healthy ever since, making it one of the few success stories of wildlife conservation worldwide.

Australia’s mammal extinction crisis

However Australia’s medium-sized mammals have had to deal with a different range of issues to the vicuña: the introduction of feral animals, particularly cats and foxes; increased grazing pressure; altered fire regimes; the clearing of habitat for development and production; and now, the effects of climate change.

It isn’t that any of these pressures are particularly important by themselves, but the fact that many of them act in concert has had a significant impact on causing the crashes in population numbers, and increasing the risk of species becoming extinct.

For example, the crescent nailtail wallaby was once an abundant and widespread macropod of central and western Australia. The pressures of feral cats and foxes coupled with clearing for agriculture and grazing, and altered fire regimes pushed this little species over the edge and it is now classified as extinct.

The problem is also more far-reaching than we first assumed. Many people may think that animals are becoming extinct in the south of Australia where habitat destruction is quite evident.

But the populations of iconic species in the north of Australia such as the northern quoll, golden bandicoot and the Carpentarian rock-rat are also collapsing. In our lifetime populations of some species have greatly reduced in number, and others have completely disappeared in landscapes that are considered to be in excellent condition.

The golden bandicoot, listed as a vulnerable species, used to be found across much of the north of Australia. It is now only found in very small populations in the Northern Territory and on the isolated Burrow Island off the coast of Western Australia.

Time to bring back the dingo?

Further research on the impacts of fire, grazing, invasive species and climate change on Australian mammals would be extremely valuable, but ecologists recognise that crucial management decisions need to be made now.

We’ve found ourselves in a position where we have identified the threats to Australian mammal species and documented the loss of these species, the role of science must turn more directly to identifying the opportunities for assisting the survival of these mammals.

In August I chaired a panel with Professor Chris Johnson from James Cook University at the International Congress of Ecology, to discuss what management could be put in place now to help beleaguered populations of small mammals recover.

Johnson’s main focus is to bring back the top-order predator.

He believes there is now good evidence that a stable population of dingoes suppresses the numbers and activity of foxes and cats, and some other feral animal species as well.

He argues that the effect of using a top predator like the dingo to hold down populations of foxes and cats is that the total intensity of predation on smaller native mammals can be reduced.

Bringing back the dingo has many sheep and cattle farmers raising their eyebrows because the wild dogs are known to kill stock. But guardian sheepdogs can protect stock herds by fighting off dingoes if they come too close. This still allows the dingoes to have a beneficial effect in the ecosystem.

Current trials of Maremma dogs, a type of sheepdog, at Dunluce sheep station in northwest Queensland demonstrate that they can be effective dingo deterrents in a pastoral zone.

This is just one potential solution that may work in some areas. Reinstating mosaic fire regimes, where patches of land are burnt at different times to allow the land to recover in stages, and controlling grazing around sensitive habitat of endangered mammals are other potential solutions that are currently under trial in various parts of the country.

Working together

Even though science doesn’t have all the answers I believe that it is more important than ever for land managers and scientists to work together to put new management regimes on the ground.

Our scientific knowledge can provide guidelines for land managers to reduce the pressures on our biodiversity. Through monitoring how species and ecosystems respond to on-ground management we can then learn and adapt our advice to meet future challenges facing Australia’s threatened species.

We need to act now: the international community is watching Australia and we have an opportunity to show how we can apply science through collaborative agreements with land managers to reduce the threats and protect endangered species.

We’ll then be able to add Australian animals to the short list of species, like the vicuña, that have been brought back from the brink of extinction.

CJA Bradshaw

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl





Few people, many threats – Australia’s biodiversity shame

31 07 2009

bridled_nailtail_400I bang on a bit about human over-population and how it drives biodiversity extinctions. Yet, it isn’t always hordes of hungry humans descending on the hapless species of this planet  – Australia is a big place, but has few people (just over 20 million), yet it has one of the higher extinction rates in the world. Yes, most of the country is covered in some fairly hard-core desert and most people live in or near the areas containing the most species, but we have an appalling extinction record all the same.

A paper that came out recently in Conservation Biology and was covered a little in the media last week gives some telling figures for the Oceania region, and more importantly, explains that we have more than enough information now to implement sound, evidence-based policy to right the wrongs of the past and the present. Using IUCN Red List data, Michael Kingsford and colleagues (paper entitled Major conservation policy issues for biodiversity in Oceania), showed that of the 370 assessed species in Australia, 80 % of the threatened ones are listed because of habitat loss, 40 % from invasive species and 30 % from pollution. As we know well, it’s mainly habitat loss we have to control if we want to change things around for the better (see previous relevant posts here, here & here).

Kingsford and colleagues proceed to give a good set of policy recommendations for each of the drivers identified:

Habitat loss and degradation

  • Implement legislation, education, and community outreach to stop or reduce land clearing, mining, and unsustainable logging through education, incentives, and compensation for landowners that will encourage private conservation
  • Establish new protected areas for habitats that are absent or poorly represented
  • In threatened ecosystems (e.g., wetlands), establish large-scale restoration projects with local communities that incorporate conservation and connectivity
  • Establish transparent and evidence-based state of environment reporting on biodiversity and manage threats within and outside protected areas.
  • Protect free-flowing river systems (largely unregulated by dams, levees, and diversions) within the framework of the entire river basin and increase environmental flows on regulated rivers

Invasive species

  • Avoid deliberate introduction of exotic species, unless suitable analyses of benefits outweigh risk-weighted costs
  • Implement control of invasive species by assessing effectiveness of control programs and determining invasion potential
  • Establish regulations and enforcement for exchange or treatment of ocean ballast and regularly implement antifouling procedures

Climate change

  • Reduce global greenhouse gas emissions
  • Identify, assess, and protect important climate refugia
  • Ameliorate the impacts of climate change through strategic management of other threatening processes
  • Develop strategic plans for priority translocations and implement when needed

Overexploitation

  • Implement restrictions on harvest of overexploited species to maintain sustainability
  • Implement an ecosystem-based approach for fisheries, based on scientific data, that includes zoning the ocean; banning destructive fishing; adopting precautionary fishing principles that include size limits, quotas, and regulation with sufficient resources based on scientific assessments of stocks and; reducing bycatch through regulation and education
  • Implement international mechanisms to increase sustainability of fisheries by supporting international treaties for fisheries protection in the high seas; avoiding perverse subsidies and improve labelling of sustainable fisheries; and licensing exports of aquarium fish
  • Control unsustainable illegal logging and wildlife harvesting through local incentives and cessation of international trade

Pollution

  • Decrease pollution through incentives and education; reduce and improve treatment of domestic, industrial, and agriculture waste; and rehabilitate polluted areas
  • Strengthen government regulations to stop generation of toxic material from mining efforts that affects freshwater and marine environments
  • Establish legislation and regulations and financial bonds (international) to reinforce polluter-pays principles
  • Establish regulations, education programs, clean ups, labelling, and use of biodegradable packaging to reduce discarded fishing gear and plastics

Disease

  • Establish early-detection programs for pathological diseases and biosecurity controls to reduce translocation
  • Identify causes, risk-assessment methods, and preventative methods for diseases
  • Establish remote communities of organisms (captive) not exposed to disease in severe outbreaks

Implementation

  • Establish regional population policies based on ecologically sustainable human population levels and consumption
  • Ensure that all developments affecting the environment are adequately analysed for impacts over the long term
  • Promote economic and societal benefits from conservation through education
  • Determine biodiversity status and trends with indicators that diagnose and manage declines
  • Invest in taxonomic understanding and provision of resources (scientific and conservation) to increase capacity for conservation
  • Increase the capacity of government conservation agencies
  • Focus efforts of nongovernmental organisations on small island states on building indigenous capacity for conservation
  • Base conservation on risk assessment and decision support
  • Establish the effectiveness of conservation instruments (national and international) and their implementation

A very good set of recommendations that I hope we can continue to develop within our governments.

CJA Bradshaw

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl





June Issue of Conservation Letters

6 06 2009