What Works in Conservation 2018

23 05 2018
P1230308

Do you have a copy of this book? If not, why not?

 

This book is free to download. This book contains the evidence for the effectiveness of over 1200 things you might do for conservation. If you don’t have a copy, go and download yourself a free one here, right now, before you even finish reading this article. Seriously. Go. You’ll laugh, you’ll cry, it’ll change your life.

Why you’ll laugh

OK, I may have exaggerated the laughing part. ‘What Works in Conservation 2018’ is a serious and weighty tome, 660 pages of the evidence for 1277 conservation interventions (anything you might do to conserve a species or habitat), assessed by experts and graded into colour-coded categories of effectiveness. This is pretty nerdy stuff, and probably not something you’ll lay down with on the beach or dip into as you enjoy a large glass of scotch (although I don’t know your life, maybe it is).

But that’s not really what it’s meant for. This is intended as a reference book for conservation managers and policymakers, a way to scan through your possible solutions and get a feel for those that are most likely to be effective. Once you have a few ideas in mind, you can follow the links to see the full evidence base for each study at conservationevidence.com, where over 5000 studies have been summarised into digestible paragraphs.

The book takes the form of discrete chapters on taxa, habitats or topics (such as ‘control of freshwater invasives’). Each chapter is split into IUCN threat categories such as ‘Agriculture’ or ‘Energy production and mining’. For each threat there are a series of interventions that could be used to tackle it, and for each of these interventions the evidence has been collated. Experts have then graded the body of the evidence over three rounds of Delphi scoring, looking at the effectiveness, certainty in the evidence (i.e., the quality and quantity of evidence available), and any harms to the target taxa. These scores combine to place each intervention in a category from ‘Beneficial’ to ‘Likely to be ineffective or harmful’. Read the rest of this entry »





Penguins cheated by ecosystem change

13 03 2018

Jorge Drexler sings “… I was committed not to see what I saw, but sometimes life is more complex than what it looks like …”*. This excerpt by the Oscar-winning Uruguayan singer seems to foretell the theme of this blog: how the ecological complexity of marine ecosystems can elicit false signals to their predators. Indeed, the fidelity of marine predators to certain feeding areas can turn demographically detrimental to themselves when the amount of available food shrinks. A study of jackass penguins illustrates the phenomenon in a context of overfishing and ocean warming.

CB_JackassPenguinsEcologicalTrapPhoto

Adult of jackass penguin (Spheniscus demersus) from Robben Island (South Africa) — in the inset, one of the first juveniles released with a satellite transmitter on its back. The species is ‘Endangered’ under IUCN’s criteria (28), following a recent halving of the total population currently estimated at ~ 80,000 adults. Jackass penguins are the only penguins living in Africa, and owe their common name to their vocalisations (you can hear their braying sounds here); adults are ~ 50 cm tall and weigh ~ 3 kg. Photos courtesy of Richard Sherley.

Surface temperature, dissolved oxygen, acidity and primary productivity are, by and large, the top four environmental factors driving the functionality of marine ecosystems (1). Growing scientific evidence supports the idea that anthropogenic warming of the atmosphere and the oceans correlates with this quartet (2). For instance, marine primary productivity is enhanced by increased temperatures (3), but a warmer sea surface intensifies stratification, i.e., stacked layers of seawater with contrasting physical and chemical properties.

In coastal areas experiencing ‘upwelling’ (where winds displace surface water, allowing deep water laden with nutrients to reach the euphotic zone where plankton communities feast), stratification weakens upwelling currents and, in turn, limits the growth of plankton (4) that fuels the entire trophic web, including our fisheries. The study of these complex trophic cascades is particularly cumbersome from the perspective of large marine predators because of their capacity to move long distances, from hundreds to thousands of kilometres (5), with strong implications for their conservation (6).

With those caveats in mind, Richard Sherley and colleagues satellite-tracked the movement of 54 post-fledged, juvenile jackass penguins (Spheniscus demersus) for 2-3 years (7). All individuals had been hatched in eight colonies (accounting for 80% of the global population), and were equipped with platform terminal transmitters. Jackass penguins currently nest in 28 island and mainland locations between South Africa and Namibia. Juveniles swim up to 2000 km in search of food and, when approaching adulthood, return to their native colonies where they reproduce and reside for the remainder of their lives (watch individuals swimming here).

The natural history of this species is linked to the Southern Hemisphere’s trade winds (‘alisios’ for Spanish speakers), which blow from the southeast to the tropics. In the South Atlantic, trade winds sustain the Benguela Current, the waters of which surface from some 300 m of depth and fertilise the marine ecosystems stretching from the Western coasts of South Africa to Angola (8). Read the rest of this entry »





Our global system-of-systems

28 02 2018

Complex-systems

I’ve just read an excellent paper that succinctly, eloquently, and wisely summarised the current predicament of our highly interconnected, global, complex adaptive system (i.e., our environment).

If you are new to the discussions around state shifts, hysteresis, tipping points, and system collapse, there might be a lot in the new paper by Philip Garnett of the University of York that you could find intimidating (and not just because of the complexity of the concepts he discusses). If you are more up-to-date on these discussions, I highly recommend reading this paper for distilling some of the more pertinent questions.

The essence of the paper is that our global environment (Earth) is one giant, complex system made up of interacting sub-systems. We can think of these as a giant, interconnected network of nodes and connections (often called ‘edges’) between them. If you do ecological network theory, then you know what I’m talking about.

What’s particularly fascinating to me is that Philip Garnett is not an environmental scientist; in fact, he’s a a lecturer in Operations Management and Business Analytics (although he does have a background in genetics and biology) who specialises in complex systems theory. In fact, much of his paper uses socio-economic examples of system complexity and collapse, yet the applications to environmentalism in general, and to ecological integrity in particular, are spot on.

Read the rest of this entry »





Offshore Energy & Marine Spatial Planning

22 02 2018

FishingOffshoreWind

I have the pleasure (and relief) of announcing a new book that’s nearly ready to buy, and I think many readers of CB.com might be interested in what it describes. I know it might be a bit premature to announce it, but given that we’ve just finished the last few details (e.g., and index) and the book is ready to pre-order online, I don’t think it’s too precocious to advertise now.

9781138954533-2

A little history is in order. The brilliant and hard-working Katherine Yates (now at the University of Salford in Manchester, UK) approached me back in 2014 to assist her with co-editing the volume that she wanted to propose for the Routledge Earthscan Ocean series. I admit that I reluctantly agreed at the time, knowing full well what was in store (anyone who has already edited a book will know what I mean). Being an active researcher in energy and biodiversity (perhaps not so much on the ‘planning’ side per se) certainly helped in my decision.

And yes, there were ups and downs, and sometimes it was a helluva lot of work, but Katherine certainly made my life easier, and she has finally driven the whole thing to completion. She deserves most of the credit.

Read the rest of this entry »





Bring it back

13 02 2018
fynbos

Protea compacta in fynbos, a form of shrubland at Soetanysberg, South Africa. Photo: Brian van Wilgen

Restoration of lost habitats and ecosystems hits all the right notes — conservation optimism, a can-do attitude, and the excitement of seeing biologically impoverished areas teem with life once more.

The Strategic Plan of the Convention on Biological Diversity includes a target to restore at least 15% of degraded ecosystems. This is being enthusiastically taken up in many places, including through initiatives such as the Bonn Challenge, a global aspiration to restore 350 million hectares of deforested and degraded land by 2030. This is in recognition of the importance of healthy ecosystems in not just conserving biodiversity, but also in combating climate change. Peatlands and forests lock away carbon, while grassland diversity stabilises ecosystem productivity during extreme weather events. So how can we make sure that these restoration efforts are as effective as possible? 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 »





Four decades of fragmentation

27 09 2017

fragmented

I’ve recently read perhaps the most comprehensive treatise of forest fragmentation research ever compiled, and I personally view this rather readable and succinct review by Bill Laurance and colleagues as something every ecology and conservation student should read.

The ‘Biological Dynamics of Forest Fragments Project‘ (BDFFP) is unquestionably one of the most important landscape-scale experiments ever conceived and implemented, now having run 38 years since its inception in 1979. Indeed, it was way ahead of its time.

Experimental studies in ecology are comparatively rare, namely because it is difficult, expensive, and challenging in the extreme to manipulate entire ecosystems to test specific hypotheses relating to the response of biodiversity to environmental change. Thus, we ecologists tend to rely more on mensurative designs that use existing variation in the landscape (or over time) to infer mechanisms of community change. Of course, such experiments have to be large to be meaningful, which is one reason why the 1000 km2 BDFFP has been so successful as the gold standard for determining the effects of forest fragmentation on biodiversity.

And successful it has been. A quick search for ‘BDFFP’ in the Web of Knowledge database identifies > 40 peer-reviewed articles and a slew of books and book chapters arising from the project, some of which are highly cited classics in conservation ecology (e.g., doi:10.1046/j.1523-1739.2002.01025.x cited > 900 times; doi:10.1073/pnas.2336195100 cited > 200 times; doi:10.1016/j.biocon.2010.09.021 cited > 400 times; and doi:10.1111/j.1461-0248.2009.01294.x cited nearly 600 times). In fact, if we are to claim any ecological ‘laws’ at all, our understanding of fragmentation on biodiversity could be labelled as one of the few, thanks principally to the BDFFP. Read the rest of this entry »





Two new postdoctoral positions in ecological network & vegetation modelling announced

21 07 2017

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With the official start of the new ARC Centre of Excellence for Australian Biodiversity and Heritage (CABAH) in July, I am pleased to announce two new CABAH-funded postdoctoral positions (a.k.a. Research Associates) in my global ecology lab at Flinders University in Adelaide (Flinders Modelling Node).

One of these positions is a little different, and represents something of an experiment. The Research Associate in Palaeo-Vegetation Modelling is being restricted to women candidates; in other words, we’re only accepting applications from women for this one. In a quest to improve the gender balance in my lab and in universities in general, this is a step in the right direction.

The project itself is not overly prescribed, but we would like something along the following lines of inquiry: 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 »





Fertilisers can make plants sicker

25 01 2017

sick-plantLast year we reported experimental evidence that the dilution effect was the phenomenon by which greater biodiversity imparts disease resistance in plant communities. Our latest paper shows the mechanism underlying this.

In my ongoing collaboration with the crack team of plant community ecologists led by Shurong Zhou at Fudan University in Shanghai, we have now shown that nitrogen-based fertilisers — in addition to causing soil damage and environmental problems from run-off — reduce a plant community’s resistance to fungal diseases.

This means that prolonged use of artificial fertilisers can lead to the extinction of the most resistant plant species in a community, meaning that the remaining species are in fact more susceptible to diseases.

Continuing the experimental field trials in alpine meadows of the Tibetan Plateau, we tested the biodiversity resilience of an isolated  plant community to increasing concentrations of nitrogenous fertilisers. In this diverse and pristine ecosystem, we have finally established that extended fertilisation of soils not only alters the structure of natural plant communities, it also exacerbates pathogen emergence and transmission. Read the rest of this entry »





Transition from the Anthropocene to the Minicene

24 09 2016
Going, going ...

Going, going … © CJA Bradshaw

I’ve just returned from a life-changing trip to South Africa, not just because it was my first time to the continent, but also because it has redefined my perspective on the megafauna extinctions of the late Quaternary. I was there primarily to attend the University of Pretoria’s Mammal Research Institute 50thAnniversary Celebration conference.

As I reported in my last post, the poaching rates in one of the larger, best-funded national parks in southern Africa (the Kruger) are inconceivably high, such that for at least the two species of rhino there (black and white), their future persistence probability is dwindling with each passing week. African elephants are probably not far behind.

As one who has studied the megafauna extinctions in the Holarctic, Australia and South America over the last 50,000 years, the trip to Kruger was like stepping back into the Pleistocene. I’ve always dreamed of walking up to a grazing herd of mammoths, woolly rhinos or Diprotodon, but of course, that’s impossible. What is entirely possible though is driving up to a herd of 6-tonne elephants and watching them behave naturally. In the Kruger anyway, you become almost blasé about seeing yet another group of these impressive beasts as you try to get that rare glimpse of a leopard, wild dogs or sable antelope (missed the two former, but saw the latter). Read the rest of this entry »





Cartoon guide to biodiversity loss XXXVIII

25 08 2016

Another six biodiversity cartoons for your midday chuckle & groan. There’s even one in there that takes the mickey out of some of my own research (see if you can figure out which one). See full stock of previous ‘Cartoon guide to biodiversity loss’ compendia here.

Read the rest of this entry »





Rich and stable communities most vulnerable to change

16 08 2016

networkI’ve just read an interesting new study that was sent to me by the lead author, Giovanni Strona. Published the other day in Nature Communications, Strona & Lafferty’s article entitled Environmental change makes robust ecological networks fragile describes how ecological communities (≈ networks) become more susceptible to rapid environmental changes depending on how long they’ve had to evolve and develop under stable conditions.

Using the Avida Digital Evolution Platform (a free, open-source scientific software platform for doing virtual experiments with self-replicating and evolving computer programs), they programmed evolving host-parasite pairs in a virtual community to examine how co-extinction rate (i.e., extinctions arising in dependent species — in this case, parasites living off of hosts) varied as a function of the complexity of the interactions between species.

Starting from a single ancestor digital organism, the authors let evolve several artificial life communities for hundred thousands generation under different, stable environmental settings. Such communities included both free-living digital organisms and ‘parasite’ programs capable of stealing their hosts’ memory. Throughout generations, both hosts and parasites diversified, and their interactions became more complex. Read the rest of this entry »





Australia pisses away the little water it has

9 05 2016

cow_drinking_australia_dryWater, water nowhere, with little left to drink.

Australians are superlative natural resource wasters, but living in the driest inhabited continent on the planet, you’d think we’d be precious about our water use.

You’d be wrong.

On the contrary, Australia has a huge water footprint (defined as “the total volume of freshwater that is used to produce the goods and services consumed by the people of the nation”). For internal domestic use (i.e., not including agricultural and industrial uses, or water imported directly or within other goods), Australians use about 341000 litres per person per year (data from 1997–2001), which is six times the global average of 57000 litres per person per year (1).

Agricultural production is one of the chief consumers of freshwater around the world. For example, the global average virtual water content of rice (paddy) is 2.29 million litres/tonne produced, and for wheat it is 1.33 litres/tonne. Growing crops for biofuel in particular has a huge water footprint — depending on the crop in question, it takes an average of 1400–20000 litres of water to produce just one litre of biofuel (2). If an agricultural product comes from livestock — say, meat, leather, or wool — the water content is typically much higher because of the feed required to keep the animal alive. For example, it takes about three years to raise beef cattle to slaughtering age, with an average of 200 kg of boneless beef produced per animal. This requires about 1,300 kg of grains, 7200 kg of pasture or hay, and 31000 litres of water for drinking and cleaning. This means that the total amount of water required to produce 1 kg of beef is about 15340 litres (1). For Australia, which has over 20 million or so cattle at any one moment, the water footprint alone should at least be cause for concern the next time you tuck into a steak dinner. Read the rest of this entry »





One-two carbon punch of defaunation

30 04 2016

1-2 punchI’ve just read a well-planned and lateral-thinking paper in Nature Communications that I think readers of CB.com ought to appreciate. The study is a simulation of a complex ecosystem service that would be nigh impossible to examine experimentally. Being a self-diagnosed fanatic of simulation studies for just such purposes, I took particular delight in the results.

In many ways, the results of the paper by Osuri and colleagues are intuitive, but that should never be a reason to avoid empirical demonstration of a suspected phenomenon because intuition rarely equals fact. The idea itself is straightforward, but takes more than a few logical steps to describe: Read the rest of this entry »





Shadow of ignorance veiling society despite more science communication

19 04 2016

imagesI’ve been thinking about this post for a while, but it wasn’t until having some long, deep chats today with staff and students at Simon Fraser University‘s Department of Biological Sciences (with a particular hat-tip to the lovely Nick Dulvy, Isabelle Côté & John Reynolds) that the full idea began to take shape in my brain. It seems my presentation was a two-way street: I think I taught a few people some things, and they taught me something back. Nice.

There’s no question at all that science communication has never before been so widespread and of such high quality. More and more scientists and science students are now blogging, tweeting and generally engaging the world about their science findings. There is also an increasing number of professional science communication associations out there, and a growing population of professional science communicators. It is possibly the best time in history to be involved in the generation and/or communication of scientific results.

Why then is the public appreciation, acceptance and understanding of science declining? It really doesn’t make much sense if you merely consider that there has never been more good science ‘out there’ in the media — both social and traditional. For the source literature itself, there has never before been as many scientific journals, articles and even scientists writing. Read the rest of this entry »





Higher biodiversity imparts greater disease resistance

12 03 2016

fungal infection

Is biodiversity good for us? In many ways, this is a stupid question because at some point, losing species that we use directly will obviously impact us negatively — think of food crops, pollination and carbon uptake.

But how much can we afford to lose before we notice anything bad is happening? Is the sort of biodiversity erosion we’re seeing today really such a big deal?

One area of research experiencing a surge in popularity is examining how variation in biodiversity (biowealth1) affects the severity of infectious diseases, and it is particularly controversial with respect to the evidence for a direct effect on human pathogens (e.g., see a recent paper here, a critique of it, and a reply).

Controversy surrounding the biodiversity-disease relationship among non-human species is less intense, but there are still arguments about the main mechanisms involved. The amplification hypothesis asserts that a community with more species has a greater pool of potential hosts for pathogens, so pathogens increase as biodiversity increases. On the contrary, the dilution hypothesis asserts that disease prevalence decreases with increasing host species diversity via several possible mechanisms, such as more host species reducing the chance that a given pathogen will ‘encounter’ a suitable host, and that in highly biodiverse communities, an infected individual is less likely to be surrounded by the same species, so the pathogen cannot easily be transmitted to a new host (the so-called transmission interference hypothesis).

So I’ve joined the ecological bandwagon and teamed up yet again with some very clever Chinese collaborators to test these hypotheses in — if I can be so bold to claim — a rather novel and exciting way.

Our new paper was just published online in EcologyWarming and fertilization alter the dilution effect of host diversity on disease severity2. Read the rest of this entry »





Biowealth

24 02 2016

frogWhile I’ve blogged about this before in general terms (here and here), I thought it wise to reproduce the (open-access) chapter of the same name published in late 2013 in the unfortunately rather obscure book The Curious Country produced by the Office of the Chief Scientist of Australia. I think it deserves a little more limelight.

As I stepped off the helicopter’s pontoon and into the swamp’s chest-deep, tepid and opaque water, I experienced for the first time what it must feel like to be some other life form’s dinner. As the helicopter flittered away, the last vestiges of that protective blanket of human technological innovation flew away with it.

Two other similarly susceptible, hairless, clawless and fangless Homo sapiens and I were now in the middle of one of the Northern Territory’s largest swamps at the height of the crocodile-nesting season. We were there to collect crocodile eggs for a local crocodile farm that, ironically, has assisted the amazing recovery of the species since its near-extinction in the 1960s. Removing the commercial incentive to hunt wild crocodiles by flooding the international market with scar-free, farmed skins gave the dwindling population a chance to recover.

redwoodConservation scientists like me rejoice at these rare recoveries, while many of our fellow humans ponder why we want to encourage the proliferation of animals that can easily kill and eat us. The problem is, once people put a value on a species, it is usually consigned to one of two states. It either flourishes as do domestic crops, dogs, cats and livestock, or dwindles towards or to extinction. Consider bison, passenger pigeons, crocodiles and caviar sturgeon.

As a conservation scientist, it’s my job not only to document these declines, but to find ways to prevent them. Through careful measurement and experiments, we provide evidence to support smart policy decisions on land and in the sea. We advise on the best way to protect species in reserves, inform hunters and fishers on how to avoid over-harvesting, and demonstrate the ways in which humans benefit from maintaining healthy ecosystems. Read the rest of this entry »








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