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 »





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.

Read the rest of this entry »





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 »





Job: Research Fellow in Palaeo-Ecological Modelling

13 04 2017

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I have another postdoctoral fellowship to advertise! All the details you need for applying are below.

KEY PURPOSE 

Scientific data such as fossil and archaeological records used as proxy to reconstruct past environments and biological communities (including humans) are sparse, often ambiguous or contradictory when establishing any consensus on timing or routes of initial human arrival and subsequent spread, the timing or extent of major changes in climate and other environmental perturbations, or the timing or regional pattern of biological extinctions.

The Research Fellow (Palaeo-Ecological Modelling) will assist in addressing these problems by developing state-of-the-art analytical and simulation tools to infer regional pattern of both the timing of human colonisation and megafauna extinction based on incomplete and sparse dataset, and investigating past environmental changes and human responses to identify their underlying causes and consequences on Australia’s landscapes, biodiversity and cultural history.

ORGANISATIONAL ENVIRONMENT 

The position will be based in the School of Biological Sciences in the Faculty of Science & Engineering at Flinders University. Flinders University boasts a world-class Palaeontology Research Group (PRG) and the new Global Ecology Research Laboratory that have close association with the research-intensive South Australian Museum. These research groups contribute to building a dynamic research environment that explores the continuum of environmental and evolutionary research from the ancient to modern molecular ecology and phylogeography. The School of Biological Sciences is an integrated community researching and teaching biology, and has a long history of science innovation. The appointee will join an interdisciplinary school of approximately 45 academic staff. The teaching and research activities of the School are supported by a range of technical and administrative infrastructure services.

KEY RESPONSIBILITIES

The key responsibilities and selection criteria identified for this position should be read in conjunction with the Flinders University Academic Profiles for the relevant academic classification (scroll down to Academic Profiles).

The Research Fellow (Palaeo-Ecological Modelling) will work under the direction of the Project Chief Investigator, and will be required to: Read the rest of this entry »





Limited nursery replenishment in coral reefs

27 03 2017
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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 »





Palaeo-ecology PhD scholarships

1 03 2017

scholarshipWith my new position as Matthew Flinders Fellow in Global Ecology at Flinders University, I am in the agreeable position to be able to offer two PhD scholarships to the best candidates from around the world. If you feel that you’re up to the challenge, I look forward to hearing from you.

These projects will be in the following palaeo-ecology topics:

PhD Project #1. Ecological networks to examine community cascades of Late Quaternary megafauna extinctions Read the rest of this entry »