It’s all about the variation, stupid

12 01 2015

val-1-3It is one of my long-suffering ecological quests to demonstrate to the buffoons in government and industry that you can’t simply offset deforestation by planting another forest elsewhere. While it sounds attractive, like carbon offsetting or even water neutrality, you can’t recreate a perfectly functioning, resilient native forest no matter how hard you try.

I’m not for a moment suggesting that we shouldn’t reforest much of what we’ve already cut down over the last few centuries; reforestation is an essential element of any semblance of meaningful terrestrial ecological restoration. Indeed, without a major commitment to reforestation worldwide, the extinction crisis will continue to spiral out of control.

What I am concerned about, however, is that administrators continue to push for so-called ‘biodiversity offsets’ – clearing a forest patch here for some such development, while reforesting or even afforesting another degraded patch there. However, I’ve blogged before about studies, including some of my own, showing that one simply cannot replace primary forests in terms of biodiversity and long-term carbon storage. Now we can add resilience to that list.

While I came across this paper a while ago, I’ve only found the time to blog about it now. Published in PLoS One in early December, the paper Does forest continuity enhance the resilience of trees to environmental change?1 by von Oheimb and colleagues shows clearly that German oak forests that had been untouched for over 100 years were more resilient to climate variation than forests planted since that time. I’ll let that little fact sink in for a moment … Read the rest of this entry »





Ecology is a Tower of Babel

17 09 2012

The term ‘ecology’ in 16 different languages overlaid on the oil on board ‘The Tower of Babel’ by Flemish Renaissance painter Pieter Bruegel the Elder (1563).

In his song ‘Balada de Babel’, the Spanish artist Luis Eduardo Aute sings several lyrics in unison with the same melody. The effect is a wonderful mess. This is what the scientific literature sounds like when authors generate synonymies (equivalent meaning) and polysemies (multiple meanings), or coin terms to show a point of view. In our recent paper published in Oecologia, we illustrate this problem with regard to ‘density dependence’: a key ecological concept. While the biblical reference is somewhat galling to our atheist dispositions, the analogy is certainly appropriate.

A giant shoal of herring zigzagging in response to a predator; a swarm of social bees tending the multitudinous offspring of their queen; a dense pine forest depriving its own seedlings from light; an over-harvested population of lobsters where individuals can hardly find reproductive mates; pioneering strands of a seaweed colonising a foreign sea after a transoceanic trip attached to the hulk of boat; respiratory parasites spreading in a herd of caribou; or malaria protozoans making their way between mosquitoes and humans – these are all examples of population processes that operate under a density check. The number of individuals within those groups of organisms determines their chances for reproduction, survival or dispersal, which we (ecologists) measure as ‘demographic rates’ (e.g., number of births per mother, number of deaths between consecutive years, or number of immigrants per hectare).

In ecology, the causal relationship between the size of a population and a demographic rate is known as ‘density dependence’ (DD hereafter). This relationship captures the pace at which a demographic rate changes as population size varies in time and/or space. We use DD measurements to infer the operation of social and trophic interactions (cannibalism, competition, cooperation, disease, herbivory, mutualism, parasitism, parasitoidism, predation, reproductive behaviour and the like) between individuals within a population1,2, because the intensity of these interactions varies with population size. Thus, as a population of caribou expands, respiratory parasites will have an easier job to disperse from one animal to another. As the booming parasites breed, increased infestations will kill the weakest caribou or reduce the fertility of females investing too much energy to counteract the infection (yes, immunity is energetically costly, which is why you get sick when you are run down). In turn, as the caribou population decreases, so does the population of parasites3. In cybernetics, such a toing-and-froing is known as ‘feedback’ (a system that controls itself, like a thermostat controls the temperature of a room) – a ‘density feedback’ (Figure 1) is the kind we are highlighting here. Read the rest of this entry »