Action, not just science

25 02 2019

raised fistsIt has taken me a long time to decide to do this, but with role models like Claire Wordley, Alejandro Frid, and James Hansen out there, I couldn’t really find any more excuses.

Yes, I’ve been a strong advocate for action on biodiversity, environment and climate-change issues for a long time, and I’ve even had a few political wins in that regard with my writing and representation. I’ve even called out more than once for universities to embrace divestment from fossil fuels (to my knowledge, even my own university still has not).

While I still think these avenues are important, my ongoing observation is that things are getting worse politically, not better. That means that the normal armchair advocacy embraced by even the most outspoken academics is probably not going to be enough to elicit real political change that we — no, the planet — desperately needs.

Extinction-Rebellion-South-Australia2It is for this reason that I’ve joined the Extinction Rebellion (South Australia Chapter), especially after my friend and colleague, Dr Claire Wordley of the University of Cambridge, joined the UK Rebellion and wrote about her experiences on this very blog. That, coupled with my ongoing and mounting concern for the future Earth my daughter will inherit, requires me to take to the streets. Read the rest of this entry »





Thirsty forests

1 02 2019

Climate change is one ingredient of a cocktail of factors driving the ongoing destruction of pristine forests on Earth. We here highlight the main physiological challenges trees must face to deal with increasing drought and heat.

Forests experiencing embolism after a hot drought. The upper-left pic shows Scots (Pinus sylvestris) and black (P. nigra) pines in Montaña de Salvador (Espuñola, Barcelona, Spain) during a hot Autumn in 2015 favouring a massive infestation by pine processionary caterpillars (Thaumetopoea pityocampa) and tree mortality the following year (Lluís Brotons/CSIC in InForest-CREAF-CTFC). To the right, an individual holm oak (Quercus ilex) bearing necrotic branches in Plasencia (Extremadura, Spain) during extreme climates from 2016 to 2017, impacting more than a third of the local oak forests (Alicia Forner/CSIC). The lower-left pic shows widespread die-off of trembling aspen (Populus tremuloides) from ‘Aspen Parkland’ (Saskatchewan, Canada) in 2004 following extreme climates in western North America from 2001 to 2002 (Mike Michaelian/Canadian Forest Service). To the right, several dead aspens near Mancos (Colorado, USA) where the same events hit forests up to one-century old (William Anderegg).

A common scene when we return from a long trip overseas is to find our indoor plants wilting if no one has watered them in our absence. But … what does a thirsty plant experience internally?

Like animals, plants have their own circulatory system and a kind of plant blood known as sap. Unlike the phloem (peripheral tissue underneath the bark of trunks and branches, and made up of arteries layered by live cells that transport sap laden with the products of photosynthesis, along with hormones and minerals — see videos here and here), the xylem is a network of conduits flanked by dead cells that transport water from the roots to the leaves through the core of the trunk of a tree (see animation here). They are like the pipes of a building within which small pressure differences make water move from a collective reservoir to every neighbours’ kitchen tap.

Water relations in tree physiology have been subject to a wealth of research in the last half a decade due to the ongoing die-off of trees in all continents in response to episodes of drought associated with temperature extremes, which are gradually becoming more frequent and lasting longer at a planetary scale (1). 

Embolised trees

During a hot drought, trees must cope with a sequence of two major physiological challenges (2, 3, 4). More heat and less internal water increase sap tension within the xylem and force trees to close their stomata (5). Stomata are small holes scattered over the green parts of a plant through which gas and water exchanges take place. Closing stomata means that a tree is able to reduce water losses by transpiration by two to three orders of magnitude. However, this happens at the expense of halting photosynthesis, because the main photosynthetic substrate, carbon dioxide (CO2), uses the same path as water vapour to enter and leave the tissues of a tree.

If drought and heat persist, sap tension reaches a threshold leading to cavitation or formation of air bubbles (6). Those bubbles block the conduits of the xylem such that a severe cavitation will ultimately cause overall hydraulic failure. Under those conditions, the sap does not flow, many parts of the tree dry out gradually, structural tissues loose turgor and functionality, and their cells end up dying. Thus, the aerial photographs showing a leafy blanket of forest canopies profusely coloured with greys and yellows are in fact capturing a Dantesque situation: trees in photosynthetic arrest suffering from embolism (the plant counterpart of a blood clot leading to brain, heart or pulmonary infarction), which affects the peripheral parts of the trees in the first place (forest dieback).

Read the rest of this entry »




Influential conservation ecology papers of 2018

17 12 2018

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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 »





With a Rebel Yell, Scientists Cry ‘No, no, more!’

29 11 2018

Adrenaline makes experiences hyper-real. Everything seems to move in slow motion, apart from my heart, which is so loud that I am sure people can hear it even over the traffic.

It’s 11:03 on a sunny November morning in central London. As the green man starts to shine, I walk into the middle of the road and sit down. On either side of me, people do the same. There can only be about 50 of us sitting on this pedestrian crossing, and I murmur ‘are we enough?’

‘Look behind you,’ says a new friend.

I turn. Blackfriar’s Bridge, usually covered in cars and buses, is filling with people. Citizens walking into the road and staying there, unfurling colourful flags with hourglass symbols on them. The police film us, standing close, but make no move to arrest anyone. Later, we discover that at least some of them encourage our disobedience.

Messages start coming in — 6,000 people are here, and we’ve blocked five bridges in central London with Extinction Rebellion, protesting for action to stop climate change and species extinctions. I’m a scientist participating in my first ever civil disobedience, and for me, this changes everything.

ER1

Left to right: protestors include kids, company directors, and extinct species.

What makes a Cambridge academic — and thousands of other people — decide that sitting in a road is their best chance of being heard? In short, nothing else has got us the emissions cuts we need. The declaration that global warming is real and that greenhouse-gas emissions need to be cut came in 1988, when I was a year old. Since then, scientists have continued to be honest brokers, monitoring greenhouse gases, running models, presenting the facts to governments and to the people. And emissions have continued to climb. The 2018 IPCC report that shocked many of us into action told us we have 12 years to almost halve emissions, or face conditions incompatible with civilisation. How did we end up here? Read the rest of this entry »





Global warming causes the worst kind of extinction domino effect

25 11 2018

Dominos_Rough1-500x303Just under two weeks ago, Giovanni Strona and I published a paper in Scientific Reports on measuring the co-extinction effect from climate change. What we found even made me — an acknowledged pessimist — stumble in shock and incredulity.

But a bit of back story is necessary before I launch into describing what we discovered.

Last year, some Oxbridge astrophysicists (David Sloan and colleagues) published a rather sensational paper in Scientific Reports claiming that life on Earth would likely survive in the face of cataclysmic astrophysical events, such as asteroid impacts, supernovae, or gamma-ray bursts. This rather extraordinary conclusion was based primarily on the remarkable physiological adaptations and tolerances to extreme conditions displayed by tardigrades— those gloriously cute, but tiny (most are around 0.5 mm long as adults) ‘water bears’ or ‘moss piglets’ — could you get any cuter names?

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Found almost everywhere and always (the first fossils of them date back to the early Cambrian over half a billion years ago), these wonderful little creatures are some of the toughest metazoans (multicellular animals) on the planet. Only a few types of extremophile bacteria are tougher.

So, boil, fry or freeze the Earth, and you’ll still have tardigrades around, concluded Sloan and colleagues.

When Giovanni first read this, and then passed the paper along to me for comment, our knee-jerk reaction as ecologists was a resounding ‘bullshit!’. Even neophyte ecologists know intuitively that because species are all interconnected in vast networks linked by trophic (who eats whom), competitive, and other ecological functions (known collectively as ‘multiplex networks’), they cannot be singled out using mere thermal tolerances to predict the probability of annihilation. Read the rest of this entry »





Ecophysiological feedbacks under climate change

29 10 2018

Variability in heat tolerance among populations modifies the climate-driven periods of diurnal activity expected for ectotherm species. We illustrate this phenomenon for Iberian lizards in a paper we have just published in the Journal of Animal Ecology (blog post reproduced with permission by the Journal; see related blog).

Common wall lizard (Podarcis muralis, male) and three localities where the species is abundant in Spain, left to right including Valdesquí/Madrid (Central System), Peñagolosa/Castellón (Iberian System) and El Portalet/Huesca (The Pyrenees).

Iberia is a wonderful natural laboratory, with a complex blend of flat/hilly, open/woody and coastal/continental terrain, swept by climatic gradients of temperature and moisture. In 2013, I launched a BES-supported project about the thermal ecology of Iberian lizards and managed to drive over much of the Iberian Peninsula in fairly little time. Not being a reptile specialist myself, I was confronted by the consistent observation that lizard populations occupied very different habitats across the known distribution of each of the ~ 25 known Iberian species belonging to the family Lacertidae.

For instance, the common wall lizard (Podarcis muralis) likes water, rocks and mountains, but you can find this pencil-long reptile at the top of a summit, along the slopes or riversides of shallow and deep ravines, on little stones barely surfacing above peatland grasslands, or among the bricks of buildings. These animals must experience different local climates conditional on where they live, and adapt their thermal physiology accordingly.

Having then started a postdoc in Miguel Araújo’s lab — a world-class site for global change ecology and ‘big’ biodiversity patterns — I reviewed a sizeable body of literature looking into large-scale gradients of thermal tolerance. Most of those papers had collated (mostly) one estimate of tolerance from each of tens to thousands of species, then mapped them against regional and global metrics of climate change through sophisticated mathematical frameworks. But these studies rarely accounted for population-level thermal tolerance.

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 »





The European Union just made bioenergy worse for biodiversity

21 08 2018

bioenergy2While some complain that the European Union (EU) is an enormous, cumbersome beast (just ask the self-harming Brexiteers), it generally has some rather laudable legislative checks and balances for nature conservation. While far from perfect, the rules applying to all Member States have arguably improved the state of both European environments, and those from which Europeans source their materials.

But legislation gets updated from time to time, and not always in the ways that benefit biodiversity (and therefore, us) the most. This is exactly what’s just happened with the new EU Renewable Energy Directive (RED) released in June this year.

Now, this is the point where most readers’ eyes glaze over. EU policy discussions are exceedingly dry and boring (I’ve dabbled a bit in this arena before, and struggled to stay awake myself). But I’ll try to lighten your required concentration load somewhat by being as brief and explanatory as possible, but please stay with me — this shit is important.

In fact, it’s so important that I joined forces with some German colleagues with particular expertise in greenhouse-gas accounting and EU policy — Klaus Hennenberg and Hannes Böttcher1 of Öko-Institut (Institute of Applied Ecology) in Darmstadt — to publish an article available today in Nature Ecology and Evolution.

bioenergy4So back to the RED legislation. The original ‘RED 2009‘ covered reductions of greenhouse-gas emissions and the mitigation of negative impacts on areas of high biodiversity value, such as primary forests, protected areas, and highly biodiverse grasslands, and for areas of high carbon stock like wetlands, forests, and peatlands.

But RED 2009 was far from what we might call ‘ambitious’, because globally mandatory criteria on water, soil and social aspects for agriculture and forestry production were excluded to avoid conflicts with rules of the World Trade Organization.

Nor did RED 2009 apply to all bioenergy types, and only included biofuels used in transport, including gaseous and solid fuels, and bioliquids used for electricity, heating, and cooling. But RED 2009 requirements also applied to all raw materials sourced from agriculture and forestry, especially as forest biomass is explicitly mentioned as a raw material for the production of advanced biofuels in the RED 2009 extension from 2015.

Thus, one could conceivably call RED 2009 criteria ‘minimum safeguards’.

But as of June this year, the EU accepted a 2016 proposal to recast RED 2009 into what is now called ‘RED II’. While the revisions might look good on paper by setting new incentives in transport (advanced biofuels) and in heating and cooling that will likely increase the use of biomass sourced from forests, and by extending the directive on solid and gaseous biomass, the amendments unfortunately take some huge leaps backwards in terms of sustainability requirements.

These include the following stuff-ups: Read the rest of this entry »





Biodiversity is everyone’s responsibility

13 07 2018

Workspace: Team Of Diverse Workers Put Hands TogetherI’m not sure if many South Australians are aware of this, but the Parliamentary Inquiry into Biodiversity by the Environment, Resources and Development Committee presented a report to the 53rd Parliament of South Australia in March 2017. I thought it worthwhile reproducing their executive summary here on CB.com (I’ve highlighted the text that I deem to be rather insightful and simultaneously damning from our own elected government representatives):

This report summarises the findings and recommendations of the South Australian Parliament’s Environment, Resources and Development Committee’s inquiry into biodiversity in South Australia. Specifically, the inquiry investigated the regulatory and policy framework to determine whether it appropriately supports terrestrial and marine ecological processes, biodiversity values and abates species extinction.

The Committee found that in spite of the efforts of the State and Federal governments, industry and private landholders in South Australia, the condition of biodiversity in the State continues to decline. Species extinctions have occurred in the past and a further “extinction debt” still exists. There is no reason to believe that this trend will improve without a change to the way we approach biodiversity conservation.

A key theme to emerge from the Inquiry is that biodiversity conservation needs to be everyone’s responsibility; State and Federal government, industry, the broader community, and private landholders.

This also means that biodiversity conservation needs to occur across both public and private land, with actions coordinated at a landscape scale.

Making biodiversity conservation everyone’s responsibility requires a range of measures, including legislative reform, improved management of threats and greater involvement of the community. The provision of greater resources would yield faster results.

This report has focused on several key themes that emerged from submissions to the Inquiry.

Regulating for better biodiversity – South Australia’s legislative framework

South Australia’s current legislative framework does not provide for optimum biodiversity outcomes.

Three key issues contribute to this –

  • an out-of-date suite of environmental legislation that lacks cohesion and consistency, particularly regarding enforcement and compliance provisions;
  • inadequate and incomplete processes for identifying and protecting at-risk elements that need special measures (e.g. for protection of specific threatened species and ecological communities); and
  • inadequate consideration of biodiversity conservation in legislation that regulates human activities. In particular, there is a lack of cohesion between the environmental legislative and policy framework and land use planning, assessment and approval.
  • Statutory fragmentation of biodiversity considerations – that is, consideration of different aspects of biodiversity under different pieces of legislation – results in lack of cohesion and consistency, duplication and inefficiency, and makes it difficult to implement a landscape approach or to identify strategic opportunities and risks.

Taken as a whole, current enforcement provisions do not provide for effective and proportionate compliance action. Enforcement and compliance provisions across the relevant legislation are uneven in their approach. For example, penalties appear to be disproportionate and not risk-based (although there are some exceptions). Modern enforcement tools such as compliance orders, civil remedies and alternative penalties (such as administrative penalties, payment of damages including exemplary damages, remediation orders etc) are not included in all relevant legislation. There is some duplication in offences and inconsistency in the types of sanctions and penalty ranges.

There is an urgent need to amend the legislative framework to support any attempt to improve biodiversity outcomes.

The best approach will be based on clear, shared responsibility for biodiversity outcomes, supported by individual accountability. However, such a change will require policy development and drive.

To ensure forward momentum and improvements in the short term while developing the policy settings to support such a step-change, a staged approach could be implemented. There are various ways this could be achieved.

The Committee suggests a 3-stage approach to reforming the legislative framework. The Committee recommends the creation of a Biodiversity Expert Panel that is responsible for advancing this 3-stage approach.

  1. The first stage will involve amendments to improve operation and effectiveness of the regulatory regime within current policy settings, acknowledging that as a result of Stage 3, provisions may be altered or moved into different pieces of legislation. Amendments generally would be to the existing ‘environmental’ Acts, and primarily to the National Parks and Wildlife Act 1972 and Native Vegetation Act 1991. They would include many of the specific areas for amendment identified in EDO submissions (2011 & 2015) as well as in the SA Government submission, for example, beginning with amendments to improve current environmental legislation.
  2. Stage 2 would progress to amendments to improve integration between Acts and improve support for landholders and community participation.
  3. Stage 3 would implement a system whereby all resource use and management would be managed by one piece of legislation, with protection of biodiversity and sustainable development at its core. Provisions for protected area management, and for the scientific work involved in identifying threatened species and communities, may be contained in separate legislation.

Threats, ecological resilience and restoration

The State’s native biodiversity is facing myriad of current threats, including habitat loss and fragmentation (due to development and changing land-use), pest plants and animals, and control burn regimes. There is a need for more stringent vegetation protection, better informed and enacted control and management strategies of known pest plants and animals, and a revision of burning regimes.

Future threats to the State’s biodiversity will be largely driven by climate change impacts and the interaction with existing major threats (e.g. urbanisation and changing land use). Adequately preparing for and managing such future threats will require knowledge of projected changes and pro-active preparation for such changes.

Working with the community

Involvement of the community is an essential part of any biodiversity conservation strategy for the State. It is a foundation stone for moving to a point where biodiversity conservation is everyone’s business.

Community engagement will become increasingly important for biodiversity conservation, especially given the growing role of volunteers to support works on public land as well as the voluntary conservation efforts of private landholders. The expanding role of volunteers reenforces that biodiversity conservation is everyone’s business.

South Australia’s approach to biodiversity conversation on private land needs to be reinvigorated.

Cross cutting themes

There were several cross cutting themes identified in submissions to the Inquiry. There was broad recognition of the strong cultural and historic significance of elements of biodiversity to Aboriginal people, and that this is often poorly understood outside those communities. Continuing to identify ways for Aboriginal people to contribute to land and water management in South Australia remains a priority.

With respect to knowledge generation, critical knowledge gaps exist that need to be filled and existing knowledge is not being adequately understood, communicated or applied. From a resourcing perspective, there is concern that insufficient funds are being allocated to biodiversity conservation, which is affecting work on public and private lands.

The management of over-abundant species in South Australia remains a challenge, noting the recent impacts of long-nose fur seals in the Lower Lakes and Coorong, and ongoing concerns regarding the impact of animals such as little corellas and some species of kangaroos on negative vegetation.

 





Communicating climate change

5 06 2018

Both the uncertainty inherent in scientific data, and the honesty of those scientists who report such data to any given audience, can sow doubt about the science of climate change. The perception of this duality is engrained in how the human mind works. We illustrate this through a personal experience connecting with global environmentalism, and synthesise some guidelines to communicate the science of climate disruption by humans.

EskimoTote_English

Courtesy of Toté (www.elcomic.es)

In January 2017, the Spanish environmental magazine Quercus invited us to give a talk, at the Cabinet of Natural History in Madrid, about our article on the effects of climate change on the feeding ecology of polar bears, which made to Quercuscover in February 2017 (1) — see blog post here. During questions and debate with the audience (comprising both scientists and non-scientists), we displayed a graph illustrating combinations of seven sources of energy (coal, water, gas, nuclear, biomass, sun and wind) necessary to meet human society’s global energy needs according to Barry Brook & Corey Bradshaw (2). That paper supports the idea that nuclear energy, and to a lesser extent wind energy, offer the best cost-benefit ratios for the conservation of biodiversity after accounting for factors intimately related to energy production, such as land use, waste and climate change.

While discussing this scientific result, one member of the audience made the blunt statement that it was normal that a couple of Australian researchers supported nuclear energy since Australia hosts the largest uranium reservoirs worldwide (~1/3 of the total). The collective membership of Quercus and the Cabinet of Natural History is not suspicious of lack of awareness of environmental problems, but a different matter is that individuals can of course evaluate a piece of information through his/her own and legitimate perspective.

The stigma of hypocrisy

Indeed, when we humans receive and assimilate a piece of information, our (often not self-conscious) approach can range from focusing on the data being presented to questioning potential hidden agendas by the informer. However, the latter can lead to a psychological trap that has been assessed recently (3) — see simple-language summary of that assessment in The New York Times. In one of five experiments, a total of 451 respondents were asked to rank their opinion about four consecutive vignettes tracking the conversation between two hypothetical individuals (Becky & Amanda) who had a common friend. During this conversation, Amanda states that their friend is pirating music from the Internet, and Becky (who also illegally downloads music) can hypothetically give three alternative answers: 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 »





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 »





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 »





Microclimates: thermal shields against global warming for small herps

22 11 2017

Thermal microhabitats are often uncoupled from above-ground air temperatures. A study focused on small frogs and lizards from the Philippines demonstrates that the structural complexity of tropical forests hosts a diversity of microhabitats that can reduce the exposure of many cold-blooded animals to anthropogenic climate warming.

Luzon forest frogs

Reproductive pair of the Luzon forest frogs Platymantis luzonensis (upper left), a IUCN near-threatened species restricted to < 5000 km2 of habitat. Lower left: the yellow-stripped slender tree lizard Lipinia pulchella, a IUCN least-concerned species. Both species have body lengths < 6 cm, and are native to the tropical forests of the Philippines. Right panels, top to bottom: four microhabitats monitored by Scheffers et al. (2), namely ground vegetation, bird’s nest ferns, phytotelmata, and fallen leaves above ground level. Photos courtesy of Becca Brunner (Platymantis), Gernot Kunz (Lipinia), Stephen Zozaya (ground vegetation) and Brett Scheffers (remaining habitats).

If you have ever entered a cave or an old church, you will be familiar with its coolness even in the dog days of summer. At much finer scales, from centimetres to millimetres, this ‘cooling effect’ occurs in complex ecosystems such as those embodied by tropical forests. The fact is that the life cycle of many plant and animal species depends on the network of microhabitats (e.g., small crevices, burrows, holes) interwoven by vegetation structures, such as the leaves and roots of an orchid epiphyte hanging from a tree branch or the umbrella of leaves and branches of a thick bush.

Much modern biogeographical research addressing the effects of climate change on biodiversity is based on macroclimatic data of temperature and precipitation. Such approaches mostly ignore that microhabitats can warm up or cool down in a fashion different from that of local or regional climates, and so determine how species, particularly ectotherms, thermoregulate (1). To illustrate this phenomenon, Brett Scheffers et al. (2) measured the upper thermal limits (typically known as ‘critical thermal maxima’ or CTmax) of 15 species of frogs and lizards native to the tropical forest of Mount Banahaw, an active volcano on Luzon (The Philippines). The > 7000 islands of this archipelago harbour > 300 species of amphibians and reptiles (see video here), with > 100 occurring in Luzon (3).

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Less snow from climate change pushes evolution of browner birds

7 09 2017

© Bill Doherty

© Bill Doherty

Climate changes exert selective pressures on the reproduction and survival of species. A study of tawny owls from Finland finds that the proportion of two colour morphs varies in response to the gradual decline of snowfall occurring in the boreal region.

Someone born in the tropics who travels to the Antarctic or the Himalaya can, of course, stand the cold (with a little engineering help from clothing, however). The physiology of our body is flexible enough to tolerate temperatures alien to those of our home. We can acclimate and, if we are healthy, we can virtually reside anywhere in the world.

However, modern climate change is steadily altering the thermal conditions of the native habitats of many species. Like us, some can live up to as much heat or cold as their genetic heritage permits, because each species can express a range of morphological, physiological, and behavioural variation (plasticity). Others can modify their genetic make-up, giving way to novel species-specific features or genotypes (evolution).

When genetic changes are speedy, that is, within a few generations, we are witnessing ‘microevolution’ — in contrast to ‘macroevolution’ across geological time scales as originally reported by Darwin and Wallace (1). To date, the detection of microevolution in response to modern climate change remains elusive, and many studies claiming so seem to lack the appropriate data to differentiate microevolution from phenotypic plasticity (i.e., the capacity of a single genotype to exhibit variable phenotypes in different environments) (2, 3). Read the rest of this entry »





Human population growth, refugees & environmental degradation

7 07 2017

refugeesThe global human population is now over 7.5 billion, and increasing by about 90 million each year. This means that we are predicted to exceed 9 billion people by 2050, with no peak in site this century and a world population of up to 12 billion by 2100. These staggering numbers are the result of being within the exponential phase of population growth since last century, such that some 14% of all human beings that have ever lived on the planet are still alive today. That is taking into account about the past 200,000 years, or 10,000 generations.

Of course just like the Earth’s resources, human beings are not distributed equally around the globe, nor are the population trends consistent among regions or nations. In fact, developing nations are contributing to the bulk of the global annual increase (around 89 million per year), whereas developed nations are contributing a growth of only about 1 million each year. Another demonstration of the disparity in human population distributon is that about half of all human beings live in just seven countries (China, India, USA, Indonesia, Brazil, Pakistan, Nigeria, and Bangladesh), representing just one quarter of the world’s total land area. Read the rest of this entry »





It’s not all about temperature for corals

31 05 2017

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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.

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Spring asynchrony in migratory birds

15 05 2017

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Brent geese flock in the Limfjorden (Denmark)courtesy of Kevin Clausen. The Brent goose (Branta bernicla) is a migratory goose that breeds in Arctic coasts, as well as in northern Eurasia and the Americas, starting from late May to early June. Adults are about 0.5 m long, weigh some 2 kg and live up to 30 years. Their nests are placed in the ground, where reproductive pairs incubate a single clutch (≤ 5 eggs) for a couple of months. They are herbivores, feeding on algae (mainly Zostera marina in Limfjord) and seagrass in estuaries, fjords, intertidal areas and rocky beaches during fall and winter. During summer they feed on tundra herbs, moss, lichens, as well as aquatic plants in rivers and lakes. The species is ‘Least Concern’ for the IUCN, with a global population at some 600,000 individuals.

Migratory birds synchronise their travel from non-breeding to breeding quarters with the seasonal conditions optimal for reproduction. Above all, they decide when to migrate on the basis of the climate of their wintering areas while they are there. As climate change involves earlier springs in the Arctic but not in the wintering areas, there is a lack of synchronisation that leads to a demographic decline of these birds in the polar regions where they breed.

When I think about how species respond to climate change, the song from the ClashShould I stay or should I go” comes to mind. As climate changes, species eventually have to face an ultimate choice: (i) stay and adapt to novel conditions or become locally extinct if adaptation fails, (ii) or move to other regions where climatic conditions should be more suitable. Migratory species have to face this decision every time they have to move back and forth from non-breeding to breeding grounds.

Migration is a behavioural strategy shared by different animal groups like sea turtles, mammals, amphibians, insects or birds. Species move from one area to another usually to feed and reproduce in the best climatic conditions possible. For birds, migration is a common phenomenon that typically entails large movements between breeding and wintering grounds. These vertebrates boast some of the longest migratory distances known in the animal kingdom, particularly seabirds like Artic terns, which can complete up to a round-world trip in a single migratory event between the UK and the Antarctic (1). There are several theories about the mechanisms triggering bird migration, including improving body condition and fitness through unexploited resources (2), reducing parasite load (3), minimizing predation risk (4), maximizing day-light (5), or reducing competition (6, 7). Whatever the cause, birds have to decide when the best moment to migrate is, counting only with the (usually climatic) clues they have at the departure site. Read the rest of this entry »





Noses baffled by ocean acidification

18 04 2017

Clown fish couple (Amphiprion percula) among the tentacles of anemone Heteractis magnifica in Kimbe Bay (Papua New Guinea) – courtesy of Mark McCormick. Clownfish protect anemones from predators and parasites in exchange of shelter and food. The fish tolerates the host’s venom because its skin is protected by a mucus layer some 2-3× thicker than phylogenetically related species (12); clownfish fabricate the mucus themselves and seem to obtain anemone antigens through a period of acclimation (13), but whether protection is acquired or innate is still debated. Clownfish are highly social bony fish, forming groups with one reproductive pair (up to 11 cm in length each) and several smaller, non-reproductive males. Reproduction is protandrous (also known as sequential hermaphroditism), so larvae are born male and, as soon as the reproductive female dies, her widower becomes female and the largest of the subsidiary males becomes the alpha male. The IUCN lists clownfish, generically named ‘anemone fish’, as threatened by the pet-trade industry and habitat degradation, although surprisingly, only 1 species has been assessed (A. sandaracinos). The clown anemone fish A. ocellaris is the species that inspired Nemo in the 2003 Academy-Award fiction movie – contrary to the logical expectation that the Oscars Red Carpet would generate support for conservation on behalf of Hollywood, of the 1568 species represented in the movie, only 16 % of those evaluated are threatened (14).

Smell is like noise, the more scents we breathe in one sniff, the more difficult it is to distinguish them to the point of olfactory saturation. Experimental work with clownfish reveals that the increase in dissolved carbon dioxide in seawater, mimicking ocean acidification, alters olfactory physiology, with potential cascading effects on the demography of species.

Places such as a restaurant, a hospital or a library have a characteristic bouquet, and we can guess the emotional state of other people by their scents. Smell is critical between predators and prey of many species because both have evolved to detect each other without the aid of vision. At sea, the smell of predators dissolves in water during detection, attack, capture, and ingestion of prey, and many fishes use this information to assess the risk of ending up crunched by enemy teeth (1, 2). But predator-prey interactions can be modified by changes in the chemical composition of seawater and are therefore highly sensitive to ongoing ocean acidification (see global measuring network here). Experts regard ocean acidification as the ‘other CO2 problem’ of climate change (3) — just to emphasize that anthropogenic climate-change impacts terrestrial and aquatic ecosystems alike. Acidification occurs because the ocean absorbs CO2 at a rate proportional with the concentration of this gas in the atmosphere and, once dissolved, CO2 becomes carbonic acid (H2CO3), which in turn releases protons (H+) — in simple terms, pH is the concentration of protons (see video about ocean acidification): Read the rest of this entry »





Not 100% renewable, but 0% carbon

5 04 2017

635906686103388841-366754148_perfection1Anyone familiar with this blog and our work on energy issues will not be surprised by my sincere support of nuclear power as the only realistic solution to climate change in the electricity (and possibly transport and industrial heat) arena. I’ve laid my cards on the table in the peer-reviewed literature (e.g., see here, here, here, here, here & here) and the standard media, and I’ve even joined the board of a new environmental NGO that supports nuclear.

And there is hope, despite the ever-increasing human population, rising consumerism, dwindling resources, and the ubiquity of ideologically driven and ethically compromised politicians. I am hopeful for several reasons, including rising safety and reliability standards of modern nuclear technology, the continued momentum of building new fission reactors in many countries, and even the beginnings of real conversations about nuclear power (or at least, the first steps toward this) in countries where nuclear energy is currently banned (e.g., Australia). I’m also heartened by the fact that nearly every conservation scientists with whom I speak is generally supportive, or at least non-resistant, to the idea of nuclear power as part of the climate change solution. An open letter by our colleagues attests to this. In fact, every day that passes brings new evidence that we cannot ignore this solution any longer.

Even despite the evidence in support of implementing a strong nuclear component into climate change-mitigation strategies, one of the most frequent arguments for not doing so is that society can achieve all of its energy needs and simultaneously combat climate change by constructing 100% renewable-energy pathways. While it is an easy mantra to repeat because it feels right intrinsically to nearly everyone with an environmental conscience, as a scientist I also had to ask if such a monumental task is even technically feasible. Read the rest of this entry »