The dingo is a true-blue, native Australian species

7 03 2019

dingo(reproduced from The Conversation)

Of all Australia’s wildlife, one stands out as having an identity crisis: the dingo. But our recent article in the journal Zootaxa argues that dingoes should be regarded as a bona fidespecies on multiple fronts.

This isn’t just an issue of semantics. How someone refers to dingoes may reflect their values and interests, as much as the science.

How scientists refer to dingoes in print reflects their background and place of employment, and the Western Australian government recently made a controversial attempt to classify the dingo as “non-native fauna”.

How we define species – called taxonomy – affects our attitudes, and long-term goals for their conservation.

What is a dog?

Over many years, dingoes have been called many scientific names: Canis lupus dingo (a subspecies of the wolf), Canis familiaris (a domestic dog), and Canis dingo (its own species within the genus Canis). But these names have been applied inconsistently in both academic literature and government policy.

This inconsistency partially reflects the global arguments regarding the naming of canids. For those who adhere to the traditional “biological” species concept (in which a “species” is a group of organisms that can interbreed), one might consider the dingo (and all other canids that can interbreed, like wolves, coyotes, and black-backed jackals) to be part of a single, highly variable and widely distributed species.

Members of the Canis genus: wolf (Canis lupus), coyote (Canis latrans), Ethiopian wolf (Canis simensis), black-backed jackal (Canis mesomelas), dingo (Canis dingo), and a representative of the domestic dog (Canis familiaris).

Read the rest of this entry »





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 »





Cartoon guide to biodiversity loss XXXIII

18 11 2015

Six more biodiversity cartoons to hold you over until I get back from Germany next week (see full stock of previous ‘Cartoon guide to biodiversity loss’ compendia here).

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Cartoon guide to biodiversity loss XXV

8 09 2014

Here are 6 more biodiversity cartoons for your conservation-humour fix (see full stock of previous ‘Cartoon guide to biodiversity loss’ compendia here).

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World Heritage Species

17 08 2014

horseshoe crabHaving just attended the Baker & Stebbins Legacy Symposium on Invasion Genetics in Pacific Grove, California, I have had a rare bit of leisure time between my book-writing commitments and operating in conference mode. It’s summer here in California, so I’ve taken the opportunity to read a bit of The New Yorker in my accommodation. It is indeed a pleasure to have these micro-moments of ‘leisure’ reading. As it turns out though, work subjects are never far from my mind as I do this.

So it interested me greatly when I read another fantastic article in the ‘Yorker about horseshoe crabs, and their precarious state despite having survived half a billion years on this planet. While I was generally interested in the science, biomedical applications, conservation and systematics of the species, what really caught my eye was the proposal to list them as a ‘World Heritage Species’.

A what? Never heard of that classification, you say? Neither had I. Not to worry though – it doesn’t exist yet. Read the rest of this entry »





Cartoon guide to biodiversity loss XXIV

17 06 2014

Another 6 biodiversity cartoons for your conservation giggle & groan (see full stock of previous ‘Cartoon guide to biodiversity loss’ compendia here).

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All that glitters is not gold – ecological traps

27 09 2011

Another corker from Salvador Herrando-Pérez:

Cinema fans know that choosing a movie by the newspaper’s commentary or the promotional poster might be a lottery. In the movie of nature, to confuse ‘the attractive’ with ‘the appropriate’ can compromise the life of an individual and its offspring, even to the extent of anticipating the extinction of an entire population or species.

Animals make daily choices about when, where or with whom to engage in basic activities like eating, hibernating, mating, migrating or resting. Those choices are often strongly tied to highly specific cues – e.g., air temperature, tree density, location of water, or smell of other individuals. And it happens to hair lice jumping from head to head among school kids, or to caribou forming their winter herds prior to the seasonal migration. All species, without exception, persist in nature because those ‘choices’ translate into survival or successful reproduction more often than do not. They are a kind of evolutionary memory imprinted in an organism’s genes and behaviour. However, sometimes the right choice (‘right’ meaning perceiving a cue for the role it actually has in the life cycle) places an individual in the worst of all possible situations. The environment cheats, ‘the attractive’ merely mimics ‘the appropriate’, and the individual fails to reproduce, starves, sickens, or even dies.

Figure 1. Water reservoirs tainted with fuel (see dark contours) in Kuwait following the Gulf War in the early 1990s. Overlaid pictures show the silhouettes of trapped odonates (right), vertebrates (top left) and invertebrates (bottom left) (Photos courtesy of Jochen Zeil).

At the mercy of mirages

During the Gulf War, the destruction of infrastructure for crude exploitation spilled large amounts of fuel in many water reservoirs over the desert landscape of Kuwait. A little later, Horváth and Zeil1 found agglomerations of dead insects (and a range of vertebrates) along the shores of these polluted reservoirs, and observed dragonflies drowning in their kamikaze attempt to spawn on the oily surface (Figure 1). This work stimulated further research whereby Horváth and his team in Budapest showed that odonates are attracted by light polarization at the surface of oiled water2 – hence ‘polarized light pollution’3. Not only that, they recorded insects struggling to spawn on or mate with riveting surfaces such as solar panels, asphalted roads, plastic bags or (creepy enough!) cemetery crypts4. It goes without saying: these insects are victims of a mirage.

Those habitats or features of the habitat that mislead an animal’s choice, often hampering the completion of its life cycle, are known as ‘ecological traps’ – in other words, the environmental cue is decoupled from the quality of the habitat it is meant to signal. Ecological traps were first described in the 1970s by Dwernychuk and Boag5. They found that ducks on the islands of Miquelon lake located their nests among those of seagulls despite the latter happily devoured their ducklings and eggs. When these islands emerged in the middle of last century, they were first colonized by common terns (Sterna hirundo). By defending their own nests ferociously from predators (mainly crows and magpies), the terns inadvertently shielded the nests of their ducky comrades. The Canadians hypothesized that when seagulls subsequently replace terns, the ducks continued to sense their new neighbours as a (now misleading) sign of protection. Read the rest of this entry »





Evolution here and now

17 02 2011

Here’s a guest post from one of my PhD students, Salvador Herrando-Peréz. Salva is working on theoretical aspects of density feedback mechanisms among different species, and is especially eclectic with his interests in biology. Salva regularly contributes to lay natural history magazines, especially in his native tongue Castellano (Spanish), and he is an active member of the Spanish organisation Bioestudios Saganta, a non-profit national organisation fully devoted to scientific research and its popularisation with a focus on biodiversity conservation.

I’ve asked my students to start contributing to ConservationBytes.com, and Salva is leading the charge.

Evolution evokes ideas such as fossils, geological eras and time scales of hundreds of thousands to millions of years. Only recently have we started to appreciate that such ‘macro-evolution’ is the result of accumulated changes in the morphology and genes of species from one generation to the next: days for HIV strands, months for a planktonic rotifer, or years for a poplar.

The Britons Peter and Rose Mary Grant published in 2002 a 30-year study on Darwin’s finches from Daphne Major (Galapagos, Ecuador) – a popular study organism since Charles Darwin’s Origin of species (Grant & Grant 2002). In such a short period of time, covering only six generations of these granivorous birds, several extreme droughts altered the type and abundance of seeds, and potentially triggered the evolution of body size, and beak shape and size, up to three times (Figure 1). The two biologists from Princeton reveal that:

  1. evolution is reversible – generations of finches experiencing overall increase in body and beak sizes can lead to future generations with smaller sizes (of course within limits; a finch will never develop the beak of a stork or a hummingbird), and
  2. phenological shifts across generations are unpredictable in so far as they respond to random climatic fluctuations – should droughts of contrasting intensity have occurred in different years over the study period, beaks and bodies might have evolved in other particular fashions. Read the rest of this entry »




Long, deep and broad

24 08 2010

© T. Holub Flickr

Thought that would get your attention ;-)

More scientists need to be trained in quantitative synthesis, visualization and other software tools.” D. Peters (2010)

In fact, that is part of the title of today’s focus paper in Trends in Ecology and Evolution by D. Peters – Accessible ecology: synthesis of the long, deep,and broad.

As a ‘quantitative’ ecologist (modeller, numerate, etc.) whose career has been based to a large degree on the analysis of large ecological datasets, I am certainly singing Peters’ tune. However, it’s much deeper and more important than my career – good (long, deep, broad – see definitions below) ecological data are ESSENTIAL to avoid some of the worst ravages of biodiversity loss over the coming decades and centuries. Unfortunately, investment in long-term ecological studies is poor in most countries (Australia is no exception), and it’s not improving.

But why are long-term ecological data essential? Let’s take a notable example. Climate change (mainly temperature increases) measured over the last century or so (depending on the area) has been determined mainly through the analysis of long-term records. This, one of the world’s most important (yet sadly, not yet even remotely acted upon) issues today, derives from relatively simple long-term datasets. Another good example is the waning of the world’s forests (see posts herehere and here for examples) and our increasing political attention on what this means for human society. These trends can only be determined from long-term datasets.

For a long time the dirty word ‘monitoring’ was considered the bastion of the uncreative and amateur – ‘real’ scientists performed complicated experiments, whereas ‘monitoring’ was viewed mainly as a form of low-intellect showcasing to please someone somewhere that at least something was being done. I’ll admit, there are many monitoring programmes producing data that aren’t worth the paper their printed on (see a good discussion of this issue in ‘Monitoring does not always count‘), but I think the value of good monitoring data has been mostly vindicated. You see, many ecological systems are far too complex to manipulate easily, or are too broad and interactive to determine much with only a few years of data; only by examining over the ‘long’ term do patterns (and the effect of extremes) sometimes become clear.

But as you’ll see, it’s not just the ‘long’ that is required to determine which land- and sea-use decisions will be the best to minimise biodiversity loss – we also need the ‘deep’ and the ‘broad’. But first, the ‘long’. Read the rest of this entry »





Life and death on Earth: the Cronus hypothesis

13 10 2009
Cronus

Cronus

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

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

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

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

Ok. Quite an aim.

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

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

Gaia

Gaia

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

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

Medea

Medea

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

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

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

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

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

CJA Bradshaw

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

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Evolution of biodiversity: the hard evidence

25 09 2009

Just a plug for Richard Dawkins’ new book “The Greatest Show on Earth“. Hard to believe, but there are still billions of people who are blind to how life actually works, mainly from the intellectual blindfold of religion.

For more things Dawkins, visit http://richarddawkins.net/.