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Tags: Australia, bounty, displacement, exploitation, extinction, farming, hunting, livestock, model, Predation, predator, prey, Tasmania, Tasmanian tiger, Thylacine
Categories : Australia, conservation, decline, deforestation, exploitation, extinction, function, habitat loss, harvest, livestock, mammal, modelling, population dynamics, population viability analysis, predator, PVA, synergies
It’s human nature to abhor admitting an error, and I’d wager that it’s even harder for the average person (psycho- and sociopaths perhaps excepted) to admit being a bastard responsible for the demise of someone, or something else. Examples abound. Think of much of society’s unwillingness to accept responsibility for global climate disruption (how could my trips to work and occasional holiday flight be killing people on the other side of the planet?). Or, how about fishers refusing to believe that they could be responsible for reductions in fish stocks? After all, killing fish couldn’t possibly …er, kill fish? Another one is that bastion of reverse racism maintaining that ancient or traditionally living peoples (‘noble savages’) could never have wiped out other species.
If you’re a rational person driven by evidence rather than hearsay, vested interest or faith, then the above examples probably sound ridiculous. But rest assured, millions of people adhere to these points of view because of the phenomenon mentioned in the first sentence above. With this background then, I introduce a paper that’s almost available online (i.e., we have the DOI, but the online version is yet to appear). Produced by our extremely clever post-doc, Tom Prowse, the paper is entitled: No need for disease: testing extinction hypotheses for the thylacine using multispecies metamodels, and will soon appear in Journal of Animal Ecology.
Of course, I am biased being a co-author, but I think this paper really demonstrates the amazing power of retrospective multi-species systems modelling to provide insight into phenomena that are impossible to test empirically – i.e., questions of prehistoric (and in some cases, even data-poor historic) ecological change. The megafauna die-off controversy is one we’ve covered before here on ConservationBytes.com, and this is a related issue with respect to a charismatic extinction in Australia’s recent history – the loss of the Tasmanian thylacine (‘tiger’, ‘wolf’ or whatever inappropriate eutherian epithet one unfortunately chooses to apply). Read the rest of this entry »
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Tags: behaviour, conservation biology, Critically Endangered, population dynamics, predator, wildlife
Categories : biodiversity, captive breeding, China, conservation, decline, exploitation, IUCN, mammal, population dynamics, research, threatened species
|Unique in its genus, the saiga antelope inhabits the steppes and semi-desert environments in two sub-species split between Kazakhstan (Saiga tatarica tatarica, ~ 80% of the individuals) and Mongolia (Saiga tatarica mongolica). Locals hunt them for their meat and the (attributed) medicinal properties of male horns. Like many ungulates, the population is sensitive to winter severity and summer drought (which signal seasonal migrations of herds up to 1000 individuals). But illegal poaching has reduced the species from > 1 million in the 1970s to ~ 50000 currently (see RT video). The species has gone extinct in China and Ukraine, and has been IUCN “Critically Endangered” from 2002. The photo shows a male in The Centre for Wild Animals, Kalmykia, Russia (courtesy of Pavel Sorokin).
In a planet approaching 7 billion people, individual identity for most of us goes largely unnoticed by the rest. However, individuals are important because each can promote changes at different scales of social organisation, from families through to associations, suburbs and countries. This is not only true for the human species, but for any species (1).
It is less than two decades since many ecologists started pondering the ways of applying the understanding of how individuals behave to the conservation of species (2-9), which some now refer to as ‘conservation behaviour’ (10, 11). The nexus seems straightforward. The decisions a bear or a shrimp make daily to feed, mate, move or shelter (i.e., their behaviour) affect their fitness (survival + fertility). Therefore, the sum of those decisions across all individuals in a population or species matters to the core themes handled by conservation biology for ensuring long-term population viability (12), i.e., counteracting anthropogenic impacts, and (with the distinction introduced by Cawley, 13) reversing population decline and avoiding population extinction.
To use behaviour in conservation implies that we can modify the behaviour of individuals to their own benefit (and mostly, to the species’ benefit) or define behavioural metrics that can be used as indicators of population threats. A main research area dealing with behavioural modification is that of anti-predator training of captive individuals prior to re-introduction. Laden with nuances, those training programs have yielded contrasting results across species, and have only tested a few instances of ‘success’ after release into the wild (14). For example, captive black-tailed prairie dogs (Cynomys ludovicianus) exposed to stuffed hawks, caged ferrets and rattlesnakes had higher post-release survival than untrained individuals in the grasslands of the North American Great Plains (15). A clear example of a threat metric is aberrant behaviour triggered by hunting. Eleanor Milner-Gulland et al. (16) have reported a 46 % reduction in fertility rates in the saiga antelope (Saiga tatarica) in Russia from 1993-2002. This species forms harems consisting of one alpha male and 12 to 30 females. Local communities have long hunted this species, but illegal poaching for horned males from the early 1990s (17) ultimately led to harems with a female surplus (with an average sex ratio up to 100 females per male!). In them, only a few dominant females seem to reproduce because they engage in aggressive displays that dissuade other females from accessing the males. Read the rest of this entry »
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Tags: Complex system, Ecosystem, macroalgae, predator, productivity, resilience, Seaweed, stability
Categories : algae, biodiversity, coasts, conservation, function, kelp, marine
© C. Hilton
Here at ConservationBytes.com, My contributors and I have highlighted the important regulating role of predators in myriad systems. We have written extensively on the mesopredator release concept applied to dingos, sharks and coyotes, but we haven’t really expanded on the broader role of predators in more complex systems.
This week comes an elegant experimental study (and how I love good experimental evidence of complex ecological processes and how they affect population persistence and ecosystem stability, resilience and productivity) demonstrating, once again, just how important predators are for healthy ecosystems. Long story short – if your predators are not doing well, chances are the rest of the ecosystem is performing poorly.
Today’s latest evidence comes from on an inshore marine system in Ireland involving crabs (Carcinus maenas), whelks (Nucella lapillus), gastropd grazers (Patella vulgata, Littorina littorea and Gibbula umbilicalis), mussels (Mytilus edulis) and macroalgae. Published in Journal of Animal Ecology, O’Connor and colleagues’ paper (Distinguishing between direct and indirect effects of predators in complex ecosystems) explains how their controlled experimental removals of different combinations of predators (crabs & whelks) and their herbivore prey (mussels & gastropods) affected primary producer (macroalgae) diversity and cover (see Figure below and caption from O’Connor et al.). Read the rest of this entry »