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Animating models of ecological change

6 12 2021

Flinders University Global Ecology postdoc, Dr Farzin Shabani, recently created this astonishing video not only about the results of his models predicting vegetation change in northern Australia as a function of long-term (tens of thousands of years) climate change, but also on the research journey itself!

He provides a brief background to how and why he took up the challenge:

Science would be a lot harder to digest without succinct and meaningful images, graphs, and tables. So, being able to visualise both inputs and outputs of scientific models to cut through the fog of data is an essential element of all science writing and communication. Diagrams help us understand trends and patterns much more quickly than do raw data, and they assist with making comparisons.

During my academic career, I have studied many different topics, including natural hazards (susceptibility & vulnerability risks), GIS-based ensemble modelling, climate-change impacts, environmental modelling at different temporal and spatial scales, species-distribution modelling, and time-series analysis. I use a wide range of graphs, charts, plots, maps and tables to transfer the key messages.

For my latest project, however, I was given the opportunity to make a short animation and visualise my results and the journey itself. I think that my animation inspires a sense of wonder, which is among the most important goals of science education. I also think that my animation draws connections to real-life problems (e.g., ecosystem changes as a product of climate change), and also develops an appreciation of the scientific process itself.

Take a look at let me know what you think!

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Tags: climate change, community ecology, forests, global dynamic vegetation model, LPJ-GUESS, paleaoecology, pollen, savanna
Categories : Australia, bottom-up ecology, climate change, community ecology, ecology, ecosystem, fire, mathematics, modelling, research, science, science communication, science writing, scientific writing, vegetation

Global warming causes the worst kind of extinction domino effect

25 11 2018

Dominos_Rough1-500x303 Just 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 tardigrades¹— 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 »

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Tags: annihilation, catastrophe, climate change, co-extinctions, community ecology, Complex systems, ecological networks, extinction, extinction cascades, Global warming, modelling, network theory, nuclear winter, tardigrades, virtual Earth
Categories : bottom-up ecology, climate change, climate shift, community ecology, conservation, conservation ecology, ecology, extinction, extinction debt, extinction vortex, modelling, top-down ecology

Fertilisers can make plants sicker

25 01 2017

sick-plant Last 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 »

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Tags: China, community ecology, dilution effect, disease, ecosystem services, Tibetan plateau
Categories : Asia, biowealth, China, conservation, ecology, ecosystem, ecosystem function, ecosystem services, extinction, function

Influential conservation ecology papers of 2016

16 12 2016

As I have done for the last three years (2015, 2014, 2013), here’s another retrospective list of the top 20 influential conservation papers of 2016 as assessed by experts in F1000 Prime.

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Tags: Anthropocene, bees, biodiversity, carbon, carbon storage, China, climate change, climatic debt, community ecology, competition, coral reefs, decline, defauntation, deforestation, ecosystem services, ecosystems, extinction, Fertiliser, forests, microbes, microbial diversity, mutualism, neonicotinoids, nutrient loading, nutrients, plant diversity, pollination, Soil, species loss, Species richness, sustainability, time series
Categories : conservation

Rich and stable communities most vulnerable to change

16 08 2016

I’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 »

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Tags: biodiversity, co-extinctions, community ecology, ecological network, Extinctions, host, parasite, resilience, stability
Categories : biodiversity, bottom-up ecology, climate change, conservation, ecology, ecosystem function, evolution, exploitation, extinction, function, invasive species

High-altitude ecology

28 08 2014

A constant hazard in the Tibetan Plateau – yakjam

I’ve been out of the social-media loop for a few weeks, hence the abnormally long interval since my last post. As you might recall, I’ve been travelling overseas and most recently blogged from Monterey, California where I was attending a symposium on invasion genetics.

The next phase of my travels couldn’t have been more different.

The reason I couldn’t access the blog was because I was well behind the Great Firewall of China. I was, in fact, in the Tibetan region of Gansu and Sichuan Provinces in western China for most of the last 10 days. While I’ve travelled to China many times before, this was by far the most evocative, interesting and unique experience I’ve ever had in this country. Reflecting on the past 10 days while waiting in Hong Kong for my flight back to Australia, I am still reeling a little from what I saw.

Top bloke: Jiajia Liu of Fudan University

What the hell was I doing at 3500-4000 m elevation on the Tibetan Plateau? Good question. I have been most fortunate to be included in a crack team of Chinese ecologists who have designed and implemented a most impressive set of experiments in plant community ecology. The team, led by Professor Shurong Zhou and Dr. Jiajia Lui of Fudan University, has been working relentlessly to put together some of the sexiest plant ecology experiments going in China.

Having now so far published two papers from the some of the experiments (see here and here), my Chinese colleagues thought it was high time I visited the famous site. Situated at 3500 m in the Tibetan region of Gansu Province in western China, the Lanzhou University research station Azi Shi Yan Zhan is about a 20-hectare area of meadow fenced off from the grazing of the ubiquitous domestic yaks herded by the local Tibetans. If that sounds pretty exotic, let me assure you that it is. Read the rest of this entry »

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Tags: aggregation, asynchrony, biodiversity, biomass, China, community ecology, functional groups, functional traits, phylogenetic diversity, plants, productivity, resilience, Tibet, Tibetan plateau
Categories : Asia, biodiversity, cattle, China, climate change, conservation, ecosystem function, function, genetic diversity, great firewall of China, habitat loss, livestock, recovery, research, science

Fast-lane mesopredators

29 07 2013

Another post from Alejandro Frid (a modified excerpt from a chapter of his forthcoming book).

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I fall in love easy. Must be my Latino upbringing. Whatever it is, I have no choice on the matter. So for five years and counting, I have been passionate about lingcod (Ophiodon elongatus) and rockfish (Sebastes spp.), upper- and mid-level predatory fishes on rocky reefs of the Northeast Pacific.

Lingcod are beautiful and fierce. Rockfish are cosmic. Both taste mighty good and—surprise, surprise—have been overfished to smithereens throughout much of their range. Howe Sound, my field site near Vancouver, British Columbia, is no exception, although new protective legislation might be starting to give them some slack.

Our dive surveys¹ and earlier studies, in combination, have pieced together a story of ecosystem change. In the Howe Sound of today, lingcod rarely exceed body lengths of 80 cm. But up to 30 years ago, when overfishing had yet to inflict the full extent of its current damage, lingcod with lengths of 90 to 100 cm had been common in the area. There is nothing unique about this; most fisheries target the biggest individuals, ultimately reducing maximum body size within each species of predatory fish.

As predators shrink, the vibrant tension of predation risk slips away. The mechanism of change has a lot to do with mouth size. Predatory fishes swallow prey whole, usually head or tail first, so it is impossible for them to eat prey bigger than the width and height of their open jaws. And bigger fishes have bigger jaws, which makes them capable not only of consuming larger prey, but also of scaring bigger prey into using antipredator behaviours, such as hiding in rocky crevices. As predators shrink, big prey enter a size refuge and only small prey remain at risk, which can alter trophic cascades and other indirect species interactions. Read the rest of this entry »