Locust ecology and
evolution
Locust species, such as the infamous Desert locust,
Schistocerca gregaria (pictured above), express a
remarkable form of phenotypic plasticity known as phase
polyphenism. The expression of phase polyphenism is
mediated by changes in local population density and results
in changes in a variety of physiological, morphological and
behavioural traits, including coloration. High population
densities during outbreaks generate gregarious phase
locusts that travel in groups referred to as migratory
bands and flying swarms.
Based on my discovery of density-dependent warning coloration in
Schistocerca lineata grasshoppers, I suspected
that a similar color change in the Desert locust might
also result in the expression of density-dependent
warning coloration, with deterrence to predators
mediated by feeding on toxic host plants. Field
experiments conducted in the Sahara desert in the West
African country of Mauritania demonstrated that Desert
locust juveniles do derive toxicity to predators by
feeding on native toxic host plants. In addition, their
expression of density-dependent color change was shown
to function as a shift in anti-predator strategy from
crypsis to warning coloration in experiments with native
visually-hunting predators (Sword et al., 2000; Sword
& Simpson, 2000).
The recognition of density-dependent warning coloration in
the Desert locust provided a key insight into its
population dynamics; warning coloration at locally high
densities can reduce per capita predation and facilitate
additional population growth leading to outbreaks.
Understanding host plant-mediated deterrence in conjunction
with knowledge of local spatial resource distribution
patterns can be used in population monitoring programs to
assess the propensity of different habitats to generate
Desert locust swarms (Babah & Sword, 2004). The
ultimate goal of this work is to help locust management
organizations such as the Centre de Lutte Antiacridienne (CLAA)
[French site | Arabic site] in Mauritania reduce the
amount of time, manpower, and pesticides necessary to
manage Desert locust outbreaks. Special thanks to
Mohammed Abdallahi ould Babah and the CLAA for being
outstanding hosts during my visits to Mauritania.
Now that I am in Australia, I will be working on the Australian plague locust, Chortoicetes terminifera. Planned projects to date include a continental-scale population genetics study using DNA microsatellites to examine migration patterns, as well as studies examining the expression and genetics of behavioural phase polyphenism. I suspect that another web page exclusively dedicated to these projects will be coming soon.
Relevant publications
Simpson, S.J. & Sword, G.A. (In Press) Phase polyphenism in locusts: Mechanisms, population consequences, adaptive significance and evolution. In: Ananthakrishnan, T. & Whitman, D. (eds.) Phenotypic Plasticity of Insects: Mechanisms and Consequences.
Lovejoy, N.R.*, Mullen, S.P.*, Sword, G.A., Chapman, R.F. & Harrison, R. (2006) Ancient trans-Atlantic flight explains locust biogeography: Molecular phylogenetics of the locust genus Schistocerca. Proceedings of the Royal Society of London B. 273:767-774. (* equal contributors)
Simpson, S.J., Sword, G.A. & DeLoof, A. (2005) Advances, controversies and consensus in locust phase polyphenism research. Journal of Orthoptera Research 14:213-222.
Babah, M.A.O. & Sword, G.A. (2004) Linking locust gregarization to resource distribution patterns across a large spatial scale. Environmental Entomology 33(6):1577-1583.
Sword, G.A. (2003) To be or not to be a locust? A comparative analysis of behavioral phase change in nymphs of Schistocerca americana and S. gregaria. Journal of Insect Physiology 47(7):709-717.
Sword, G.A., Simpson, S.J., El Hadi, O.T.M. & Wilps, H. (2000) Density-dependent aposematism in the Desert locust. Proceedings of the Royal Society of London B 267:63-68.
Sword, G.A. & Simpson, S.J. (2000) Is there an intraspecific function for density-dependent color change in the Desert locust? Animal Behaviour 59: 861-870.
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