A brief history of environmentalism in Australia since European invasion

29 06 2020

A (heavily) modified and updated excerpt from our 2015 book Killing the Koala and Poisoning the Prairie

The Australian awakening to its environmental dilemmas was a little more sluggish than elsewhere in the New World. Not only did Europeans arrive in Australia en masse only about 250 years ago, they had a more limited view of their new landscape, and were, at least initially, constrained by the harshness of their new home. Those mostly British settlers brought with them the fully formed ideas of development and progress shaped by centuries of land use in the Motherland. That ideal of conquering wilderness and transforming it into the bucolic landscape typical of the English countryside was their driving force.

The early settlers viewed the Australian bush as ugly and monotonous, features that could only be overcome by human occupation and cultivation. This neo-classical view, homesickness and the Romantic desire to transform their homes and farms into an image of those from their homeland, were defining forces in early Australian history. Unlike in Europe, though, where there were cultural taboos associated with forest degradation — bound in mysticism, spirituality, folklore and politics — no such restrictions applied to the unfamiliar Australian bush.

In fact, the Australian government passed the Crown Lands Alienation Act in 1861, which was designed to ‘open up’ the colony to settlement, and penalized landholders for not clearing the land (via a forfeit of the land back to the Crown). That single Act guaranteed the deforestation wave would continue for over a 100 years. That, and the persistent desire to make the new land look as much as possible as the old, has ensured that continuing demise of Australia’s biodiversity.

Figure 3.3-Clearing for Agriculture

Clearing for agriculture in early settlement. Anonymous, Government Farm at Castle Hill, circa 1803. Watercolour, 24×35 cm. Permission to reproduce courtesy of the Mitchell Library, State Library of New South Wales

Interestingly, clashes over land use between the settlers and Indigenous peoples were probably some of the first demonstrations of what today we would call ‘environmentalism’ in Australia. Aboriginal nations were intent on preserving their way of life (and indeed, their lives) in the face of the settlers’ onslaught. But this was seen, at most, as a mild inconvenience for the new Australians who in response invoked the idea of terra nullius — that no one owned the land, making it available to anyone (white) who wished to ‘improve’ (clear) it. Read the rest of this entry »





Successful movers responding to climate change

16 06 2020

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

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

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

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

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





The state of global biodiversity — it’s worse than you probably think

24 01 2020

Chefurka biomass slide

I often find myself in a position explaining to non-professionals just how bad the state of global biodiversity really is. It turns out too that even quite a few ecologists seem to lack an appreciation of the sheer magnitude of damage we’ve done to the planet.

The loss of biodiversity that has occurred over the course of our species’ time on Earth is staggering. This loss is now truly planetary in scale and caused by human actions, albeit the severity of which is unequally distributed across the globe1. While Sandra Díaz and company recently summarised the the extent of the biodiversity crisis unfolding1 well in their recent synopsis of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services (IPBES)2 report, I’m going to repeat some of the salient summary statements here, and add a few others. Read the rest of this entry »





Influential conservation ecology papers of 2018

17 12 2018

e35f9ddeada029a053a15cd023abadf5
For the last five years I’ve published a retrospective list of the ‘top’ 20 influential papers of the year as assessed by experts in F1000 Prime — so, I’m doing so again for 2018 (interesting side note: six of the twenty papers highlighted here for 2018 appear in Science magazine). See previous years’ posts here: 2017, 20162015, 2014, and 2013.

Read the rest of this entry »





Sex on the beach

2 10 2018
Female green turtles (Chelonia mydas) spawning (top) and diving (bottom) on Raine Island (Great Barrier Reef, Queensland, Australia) — photos courtesy of Ian Bell. This species is ‘Endangered’ globally since 1982, mainly from egg harvesting (poaching conflict in Mexico for olive ridley Lepidochelys olivacea featured by National Geographic’s video here), despite the success of conservation projects (39). Green turtles inhabit tropical and subtropical seas in all oceans. Adults can grow > 150 kg and live for up to ~ 75 years. Right after birth, juveniles venture into the open sea to recruit ultimately in coastal areas until sexual maturity. They then make their first reproductive migration, often over 1000s of km (see footage of a real dive of a camera-equipped green turtle), to reach their native sandy beaches where pregnant females will lay their eggs. Each female can deposit more than one hundred eggs in her nest, and in several clutches in the same season because they can store the sperm from multiple mating events.

When sex is determined by the thermal environment, males or females might predominate under sustained climatic conditions. A study about marine turtles from the Great Barrier Reef illustrates how feminisation of a population can be partitioned geographically when different reproductive colonies are exposed to contrasting temperatures.

Fortunately, most people in Western societies already perceive that we live in a complex blend of sexual identities, far beyond the kind of genitals we are born with. Those identities start to establish themselves in the embryo before the sixth week of pregnancy. In the commonest scenario, for a human foetus XY with one maternal chromosome (X) and one paternal (Y) chromosome, the activation of the Sry gen (unique to Y) will trigger the differentiation of testicles and, via hormonal pathways, the full set of male characteristics (1).

Absence of that gene in an XX embryo will normally lead to a woman. However, in just one of many exceptions to the rule, Sry-expression failure in XY individuals can result in sterile men or ambiguous genitals — along a full gradient of intermediate sexes and, potentially, gender identities. A 2015 Nature ‘News’ feature echoes two extraordinary cases: (i) a father of four children found to bear a womb during an hernia operation, and (ii) a pregnant mother found to host both XX and XY cells during a genetic test – with her clinical geneticist stating “… that’s the kind of science-fiction material for someone who just came in for an amniocentesis” (2). These real-life stories simply reflect that sex determination is a complex phenomenon.

Three ways of doing it

In nature, there are three main strategies of sex determination (3) — see scheme here: Read the rest of this entry »





Influential conservation ecology papers of 2017

27 12 2017

Gannet Shallow Diving 03
As I have done for the last four years (20162015, 2014, 2013), here’s another retrospective list of the top 20 influential conservation papers of 2017 as assessed by experts in F1000 Prime.

Read the rest of this entry »





Tiny, symbiotic organisms protect corals from predation and disease

20 12 2017

hydrozoan polyp

Hydrozoan polyps living on the surface of a coral (photo credit: S. Montano)

Corals could have some unexpected allies to cope with the multi-faceted threats posed by climate change.

In a new study published today in Proceedings of the Royal Society B, Montano and colleagues show how tiny hydrozoans smaller than 1 mm and commonly found in dense colonies on the surface of hard corals (see above photo) play an important ecological role.

Visually examining ~ 2500 coral colonies in both Maldivian and Saudi Arabian reefs, the scientists searched for signs of predation, temperature-induced stress, and disease. For each colony, they also recorded the presence of symbiotic hydrozoans. They demonstrated that corals living in association with hydrozoans are much less prone to be eaten by corallivorous (i.e., ‘coral-eating’) fish and gastropods than hydrozoan-free corals.

A likely explanation for this pattern could be the deterring action of hydrozoan nematocysts (cells capable of ejecting a venomous organelle, which are the same kinds found in jellyfish tentacles). An individual hydrozoan polyp of less than 1 mm clearly cannot cope with a corallivorous fish that is a billions of times larger, yet hydrozoans can grow at high densities on the surface of corals (sometimes > 50 individuals per cm2). This creates a sort of a continuous, ‘urticating‘ carpet that can discourage fish from foraging. Read the rest of this entry »





It’s not all about temperature for corals

31 05 2017

CB_ClimateChange6_Photo

Three of the coral species studied by Muir (2): (a) Acropora pichoni: Pohnpei Island, Pacific Ocean — deep-water species/IUCN ‘Near threatened’; (b) Acropora divaricate: Maldives, Indian ocean — mid-water species/IUCN ‘Near threatened’; and (c) Acropora gemmifera: Orpheus Island, Australia — shallow-water species/IUCN ‘Least Concern’. The IUCN states that the 3 species are vulnerable to climate change (acidification, temperature extremes) and demographic booms of the invading predator, the crown-of-thorns starfish Acanthaster planci. Photos courtesy of Paul Muir.

Global warming of the atmosphere and the oceans is modifying the distribution of many plants and animals. However, marine species are bound to face non-thermal barriers that might preclude their dispersal over wide stretches of the sea. Sunlight is one of those invisible obstacles for corals from the Indian and Pacific Oceans.

If we were offered a sumptuous job overseas, our professional success in an unknown place could be limited by factors like cultural or linguistic differences that have nothing to do with our work experience or expertise. If we translate this situation into biodiversity terms, one of the best-documented effects of global warming is the gradual dispersal of species tracking their native temperatures from the tropics to the poles (1). However, as dispersal progresses, many species encounter environmental barriers that are not physical (e.g., a high mountain or a wide river), and whose magnitude could be unrelated to ambient temperatures. Such invisible obstacles can prevent the establishment of pioneer populations away from the source.

Corals are ideal organisms to study this phenomenon because their life cycle is tightly geared to multiple environmental drivers (see ReefBase: Global Information System for Coral Reefs). Indeed, the growth of a coral’s exoskeleton relies on symbiotic zooxanthellae (see video and presentation), a kind of microscopic algae (Dinoflagellata) whose photosynthetic activity is regulated by sea temperature, photoperiod and dissolved calcium in the form of aragonite, among other factors.

Read the rest of this entry »





Limited nursery replenishment in coral reefs

27 03 2017

Haemulon sciurus

blue-striped grunt (Haemulon sciurus)

Coral reef fishes are wonderfully diverse in size, form, and function, as well as their need for different habitats throughout the life cycle. Some species spend all of their life in the same kind of coral habitat, while others need different places to breed and feed.

Fishes requiring different habitats as they progress through life often have what we call ‘nurseries’ in which adults lay eggs and the subsequent juveniles remain, and these places are often dominated by mangroves or seagrasses (i.e., they are not part of the coral reef).

While we’ve known for quite some time that when these nursery habitats are not around, adjacent coral reefs have few, if any, of these nursery-dependent species. What we haven’t known until now is just how far the influence of nurseries extends along a coral reef.

In other words, if a nursery is present, just how many new recruits do different areas of a reef receive from it? Read the rest of this entry »





Species-area & species-accumulation curves not the same

30 05 2016

IBI’ve just read an elegant little study that has identified the main determinants of differences in the slope of species-area curves and species-accumulation curves.

That’s a bit of a mouthful for the uninitiated, so if you don’t know much about species-area theory, let me give you a bit of background for why this is an important new discovery.

Perhaps one of the only ‘laws’ in ecology comes from the observation that as you sample from larger and larger areas of any habitat type, the number of species tends to increase. This of course originates from MacArthur & Wilson’s classic book, The Theory of Island Biography (1967), and while simple in basic concept, it has since developed into a multi-headed Hydra of methods, analysis, theory and jargon.

One of the most controversial aspects of generic species-area relationships is the effect of different sampling regimes, a problem I’ve blogged about before. Whether you are sampling once-contiguous forest of habitat patches in a ‘matrix’ of degraded landscape, a wetland complex, a coral reef, or an archipelago of true oceanic islands, the ‘ideal’ models and the interpretation thereof will likely differ, and in sometimes rather important ways from a predictive and/or applied perspective. Read the rest of this entry »





It’s not always best to be the big fish

3 02 2016

obrien_fish_2Loosely following the theme of last week’s post, it’s now fairly well established that humans tend to pick on the big species first.

From fewer big trees, declines of big carnivores, elephant & rhino poaching, to fishing down the web, big species tend to cop it hardest when it comes to human-caused ecological disturbance.

While there are a lot of different combinations of traits that make some species more vulnerable to extinction than others (see examples for legumes, amphibians, sharks & teleosts, and mammals), one of the main ones is species size.

Generally speaking, larger species tend to produce fewer offspring and breed later in life than smaller species. This means that despite larger species tending to live longer than their smaller counterparts, their ‘slow’ reproductive output means that they are generally more susceptible to rapid environmental change (mainly via human intervention). In other words, their capacity for self-replacement is often too low to counteract the offtake from direct exploitation or habitat loss.

Despite a reasonable scientific understanding of this extinction-risk principle, the degree to which human disturbance affects species’ distributions is much less well quantified, and this is especially true for marine species.

I’m proud to announce another fascinating paper led by my postdoc, Camille Mellin, that has just come out online in Nature CommunicationsHumans and seasonal climate variability threaten large-bodied coral reef fish with small ranges.

With the world’s largest combined dataset of coral reef fish surveys for the entire Indo-Pacific (including the coral reef fish biodiversity hotspot — the Coral Triangle), we examined which conditions best described the distribution of fishes over a range of body sizes. Read the rest of this entry »





More species = more resilience

8 01 2014

reef fishWhile still ostensibly ‘on leave’ (side note: Does any scientist really ever take a proper holiday? Perhaps a subject for a future blog post), I cannot resist the temptation to blog about our lab’s latest paper that just came online today. In particular, I am particularly proud of Dr Camille Mellin, lead author of the study and all-round kick-arse quantitative ecologist, who has outdone herself on this one.

Today’s subject is one I’ve touched on before, but to my knowledge, the relationship between ‘diversity’ (simply put, ‘more species’) and ecosystem resilience (i.e., resisting extinction) has never been demonstrated so elegantly. Not only is the study elegant (admission: I am a co-author and therefore my opinion is likely to be biased toward the positive), it demonstrates the biodiversity-stability hypothesis in a natural setting (not experimental) over a range of thousands of kilometres. Finally, there’s an interesting little twist at the end demonstrating yet again that ecology is more complex than rocket science.

Despite a legacy of debate, the so-called diversity-stability hypothesis is now a widely used rule of thumb, and its even implicit in most conservation planning tools (i.e., set aside areas with more species because we assume more is better). Why should ‘more’ be ‘better’? Well, when a lot of species are interacting and competing in an ecosystem, the ‘average’ interactions that any one species experiences are likely to be weaker than in a simpler, less diverse system. When there are a lot of different niches occupied by different species, we also expect different responses to environmental fluctuations among the community, meaning that some species inherently do better than others depending on the specific disturbance. Species-rich systems also tend to have more of what we call ‘functional redundancy‘, meaning that if one species providing an essential ecosystem function (e.g., like predation) goes extinct, there’s another, similar species ready to take its place. Read the rest of this entry »





No more ecology

9 05 2012

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

Let me explain.

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

Bollocks.

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

Read the rest of this entry »





Marine forests dropping off the edge

21 11 2011

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 »





More than leftovers: getting marine parks right in Australia

7 08 2011

Taken by user Hossen27

Image via Wikipedia

A few weeks back I cosigned a ‘statement of concern’ about the proposal for Australia’s South West Marine Region organised by Hugh Possingham. The support has been overwhelming by Australia’s marine science community (see list of supporting scientists below). I’ve reproduced the letter addressed to the Australian government – distribute far and wide if you give more than a shit about the state of our marine environment (and the economies it supports). Basically, the proposed parks are merely a settlement between government and industry where nothing of importance is really being protected. The parks are just the leftovers industry doesn’t want. No way to ensure the long-term viability of our seas.

On 5 May 2011 the Australian Government released a draft proposal for a network of marine reserves in the Commonwealth waters of the South West bioregional marine planning region.

Australia’s South West is of global significance for marine life because it is a temperate region with an exceptionally high proportion of endemic species – species found nowhere else in the world.

Important industries, such as tourism and fisheries, depend on healthy marine ecosystems and the services they provide. Networks of protected areas, with large fully protected core zones, are essential to maintain healthy ecosystems over the long-term – complemented by responsible fisheries management1.

The selection and establishment of marine reserves should rest on a strong scientific foundation. We are greatly concerned that what is currently proposed in the Draft South West Plan is not based on the three core science principles of reserve network design: comprehensiveness, adequacy and representation. These principles have been adopted by Australia for establishing our National Reserve System and are recognized internationally2.

Specifically, the draft plan fails on the most basic test of protecting a representative selection of habitats within the bioregions of the south-west. There are no highly protected areas proposed at all in three of the seven marine bioregions lying on the continental shelf3. Overall less than 3.5% of the shelf, where resource use and biodiversity values are most intense, is highly protected. Further, six of the seven highly protected areas that are proposed on the shelf are small (< 20 km in width)4 and all are separated by large distances (> 200 km)5. The ability of such small isolated areas to maintain connectivity and fulfil the goal of protecting Australia’s marine biodiversity is limited. 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 »





Global erosion of ecosystem services

14 09 2010

A few months ago I was asked to give a lecture about erosion of ecosystem services to students in the University of Adelaide‘s Issues in Sustainable Environments unit. I gave that lecture last week and just uploaded a slidecast of the presentation (with audio) today.

I’ve reproduced the lecture here for your viewing pleasure. I hope you find the 45-minute presentation useful. Note that the first few minutes cover me referring to the Biodiversity film short that I posted not too long ago.

CJA Bradshaw





Marine protected areas: do they work?

13 08 2010

One measure that often meets great resistance from fishermen, but is beloved by conservationists, is the establishment of marine protected or ‘no take’ areas.” Stephen J. Hall (1998)

I’m going to qualify this particular post with a few disclaimers; first, I am not involved in the planning of any marine protected areas (henceforth referred to as ‘marine parks’) in Australia or elsewhere; and second, despite blogging on the issue, I have never published in the discipline of protected area design (i.e, ‘conservation planning’ is not my area of expertise).

That said, it seems to becoming more imperative that I enter the fray and assess not only how marine parks should be designed, but how effective they really are (or can be). I’ve been asked by several conservation NGOs to provide some insight into this, so I thought I should ‘think aloud’ and blog a little mini-review about marine park effectiveness.

Clearly there is a trend to establish more marine parks around the world, and this is mainly because marine conservation lags so far behind terrestrial conservation. Indeed, Spalding et al. (2008) showed that only 4.1 % of continental shelf areas are incorporated within marine parks, and ~ 50 % of all marine ecoregions have less than 1 % marine park coverage across the shelf. Furthermore, marine protection is greatest in the tropical realms, while temperate realms are still poorly represented.

The question of whether marine parks ‘work’ is, however, more complicated than it might first appear. When one asks this question, it is essential to define how the criteria for success are to be measured. Whether it’s biodiversity protection, fisheries production, recreational revenue, community acceptance/involvement or some combination of the above, your conclusion is likely to vary from place to place.

Other complications are, of course, that if you cannot ensure a marine park is adequately enforced (i.e., people don’t respect the rules) or if you don’t actually place the park anywhere near things that need protecting, there will be no real net benefit (for any of the above-mentioned interest groups). Furthermore, most marine parks these days have many different types of uses allowed in different zones (e.g., no fishing, some fishing, recreational diving only, no boat transport, some shipping, etc., etc., etc.), so it gets difficult to test for specific effects (it’s a bit like a cap-and-trade legislation for carbon – too many rules and often no real net reduction in carbon emissions – but that’s another story).

All these conditions aside, I think it’s a good idea to present what the real experts have been telling us about marine park effectiveness from a biodiversity and fishing perspective over the last decade or so. I’ll summarise some of the major papers here and give an overall assessment at the end. I do not contend that this list is even remotely comprehensive, but it does give a good cross-section of the available evidence. Read the rest of this entry »





Faraway fettered fish fluctuate frequently

27 06 2010

Hello! I am Little Fish

Swimming in the Sea.

I have lots of fishy friends.

Come along with me.

(apologies to Lucy Cousins and Walker Books)

I have to thank my 3-year old daughter and one of her favourite books for that intro. Now to the serious stuff.

I am very proud to announce a new Report in Ecology we’ve just had published online early about a new way of looking at the stability of coral reef fish populations. Driven by one of the hottest young up-and-coming researchers in coral reef ecology, Dr. Camille Mellin (employed through the CERF Marine Biodiversity Hub and co-supervised by me at the University of Adelaide and Julian Caley and Mark Meekan of the Australian Institute of Marine Science), this paper adds a new tool in the design of marine protected areas.

Entitled Reef size and isolation determine the temporal stability of coral reef fish populations, the paper applies a well-known, but little-used mathematical relationship between the logarithms of population abundance and its variance (spatial or temporal) – Taylor’s power law.

Taylor’s power law is pretty straightforward itself – as you raise the abundance of a population by 1 unit on the logarithmic scale, you can expect its associated variance (think variance over time in a fluctuating population to make it easier) to rise by 2 logarithmic units (thus, the slope = 2). Why does this happen? Because a log-log (power) relationship between a vector and its square (remember: variance = standard deviation2) will give a multiplier of 2 (i.e., if xy2, then log10x ~ 2log10y).

Well, thanks for the maths lesson, but what’s the application? It turns out that deviations from the mathematical expectation of a power-law slope = 2 reveal some very interesting ecological dynamics. Famously, Kilpatrick & Ives published a Letter in Nature in 2003 (Species interactions can explain Taylor’s power law for ecological time series) trying to explain why so many real populations have Taylor’s power law slopes < 2. As it turns out, the amount of competition occurring between species reduces the expected fluctuations for a given population size because of a kind of suppression by predators and competitors. Cool.

But that application was more a community-based examination and still largely theoretical. We decided to turn the power law a little on its ear and apply it to a different question – conservation biogeography. Read the rest of this entry »





Interview with a social (conservation) scientist

22 06 2010

I was contacted recently by Josh Cinner, a self-titled ‘social’ scientist (now working at the Centre of Excellence for Coral Reef Studies) who has published rather a lot in the conservation literature. He was recently highlighted in the journal Science for his work, and he thought CB readers would enjoy the coverage. He stated to me:

“…as a social scientist, I have spent the past decade or so working with ecologists and managers trying to integrate social science better in conservation. There are often calls for the importance of integrating social science in conservation and I thought your blog readers might appreciate some high-level recognition of the importance of this. Additionally, as far as I can tell, this is the first of these profiles that has focused on someone working in conservation.”

So, while fully crediting the source of this article and its author, Helen Fields, here is the entire text reproduced for your reading pleasure.

In the late 1980s, things were not going well for the coral reefs at Jamaica’s Montego Bay Marine Park. Overfishing had taken out a lot of the fish that eat algae, and algae were taking over the reef. “It was a classic case of ecosystem decline,” human geographer Joshua Cinner says. He arrived in Jamaica in 1996 as a Peace Corps volunteer after graduating from the University of Colorado, Boulder, with a double major in environmental conservation and geography. He was particularly interested in parks and preserves.

He’d landed in the middle of a war. Lobbying by tour operators and others got spearfishing, one of the main culprits in overfishing, banned in the park. The ban did not go over well with local people. “All the park equipment got vandalized. We had park rangers get threatened; their families got threatened at spear point,” Cinner says. Spearfishing equipment is cheap and you don’t need a boat; men who do it are generally poor and are fishing as a last resort. “The cultural lens through which the fishermen viewed this issue was of struggle in a post-slavery society, of the rich, predominantly white expatriates making a law that oppressed the poorest of the poor locals to benefit the wealthy.”

The conflict got Cinner thinking about how conservation really works. “It wasn’t really about the ecology,” he says. “Making conservation work in Jamaica had a lot to do with understanding the local culture and people.” It also opened his eyes to the role oceans play. “The ocean is often viewed as an open-access resource. That extra layer of complexity interested me,” he says. “Land can often be private property,” but “the ocean is typically viewed as free for anyone to fish in, for anyone to swim in and use.” Read the rest of this entry »