Fuel oils from euphorbs and other plants

Fuel oils from Euphorbs and other plants. The increasing energy costs of finding petroleum, together with the sure knowledge that its supply is finite, has prompted us to seek other sources of liquid hydrocarbon for both fuel and material. We have turned to annually renewable plant sources such as seed oils, an obvious source, with palm oil as the most productive. Sugar cane used to produce ethanol is another fuel source already in use.
We have examined non-food plants which can be grown on marginal soil for their productivity, particularly the genus Euphorbia. All species of this genus produce a latex which can be converted into useful fuel and other material, including precursors for what might be a valuable anti-tumor agent. Euphorbias and other similar plants require repeated planting and harvesting of the entire plant, which constitutes a drain on the soil. Trees can be long-term sources for hydrocarbon-like materials with a single planting. Examples are: the genus Copaifera which can be tapped for sesquiterpenes, the genus Pittosporum which bears fruits rich in terpenes and can be harvested annually. Finally, there are algae whose oil productivity is already of interest.
It seems possible to modify genetically the terpene biosynthetic pathways in plants to improve both the quality and quantity of the oils produced from them.     

Modelling and analysing evolution of dispersal in populations at expanding range boundaries

Abstract 1. Species would be expected to shift northwards in response to current climate warming, but many are failing to do so because of fragmentation of breeding habitats. Dispersal is important for colonisation and an individual‐based spatially explicit model was developed to investigate impacts of habitat availability on the evolution of dispersal in expanding populations. Model output was compared with field data from the speckled wood butterfly Pararge aegeria, which currently is expanding its range in Britain. 2. During range expansion, models simulated positive linear relationships between dispersal and distance from the seed location. This pattern was observed regardless of quantity (100% to 10% habitat availability) or distribution (random vs. gradient distribution) of habitat, although higher dispersal evolved at expanding range margins in landscapes with greater quantity of habitat and in gradient landscapes. Increased dispersal was no longer evident in any landscape once populations had reached equilibrium; dispersal values returned to those of seed populations. However, in landscapes with the least quantity of habitat, reduced dispersal (below that of seed populations) was observed at equilibrium. 3. Evolutionary changes in adult flight morphology were examined in six populations of P. aegeria along a transect from the distribution core to an expanding range margin in England (spanning a latitudinal distance of >200 km). Empirical data were in agreement with model output and showed increased dispersal ability (larger and broader thoraxes, smaller abdomens, higher wing aspect ratios) with increasing distance from the distribution core. Increased dispersal ability was evident in populations from areas colonised >30 years previously, although dispersal changes were generally evident only in females. 4. Evolutionary increases in dispersal ability in expanding populations may help species track future climate changes and counteract impacts of habitat fragmentation by promoting colonisation. However, at the highest levels of habitat loss, increased dispersal was less evident during expansion and reduced dispersal was observed at equilibrium indicating that, for many species, continued habitat fragmentation is likely to outweigh any benefits from dispersal.