top of page

Adaptation of woodlice to temperature change.

ABSTRACT

The ability to acclimatise to different environmental changes varies from organism to organism and thus the need to determine the survival rate of the Metanoponorthus after a shift in temperatures they are accustomed to for their physiological functions. The experimental procedure was done to determine the survival rate of two Metanoponorthus (woodlice) samples pre-exposed to temperatures of 15oC and 25oC for two weeks and acutely exposed to 45oC until they appeared to have died. The 25oC woodlice generally showed a lower mortality rate compared to the 15oC ones at the acclimation period of 1.7min; 3.35min; 9.8min and 15.75min. This may have been attributed to the ability to acclimate to higher temperatures as they had already been exposed to such for the two weeks, giving rise to the warmer-is-better hypothesis. Genetic variation may also have played a role in the high mortality rate at 9.8min interval of the acclimation period of the 25oC woodlice which opposes the proposed hypothesis.

INTRODUCTION

An organisms’ ability to accustom to a changing environment has allowed the survival of species over years and the adaptation of the species to different environments, leading to not only phenotypic but also genetic changes. These have been able to ensure survival of an organism by changes in allele frequencies (Bradshaw, 1965; Pigliucci, 2001) that best suit the environment. Exposure to acute, short term disturbances however, in conditions suitable for survival would foster an organism to acclimatise to the changes in the environment so as to maintain or improve its behavioral as physiological functions and this is termed acclimation (Prosser, 1991; Cooper et al., 2010).

The plasticity (acclimation) can lead to improvements in energy absorption (Yamori et al., 2006), heat resistance or cold resistance, locomotion (Wilson & Franklin, 2000), tolerance of the environment (Dalghaard et al., 1998) as we all as success in mating (Wilson et al., 2007). Due to such benefits, the beneficial acclimation hypothesis was proposed, which predicted acclimation improved an organisms’ performance (Leroi et al., 1994; Huey & Berrigan, 1996) when changes in the environment are introduced, although this was not always the case. This is dependent on the stress an organism is exposed to as some organisms’ performance is enhanced whilst some is impaired and thus no resistance to the change (Karl et al., 2014).

In response to the beneficial acclimation hypothesis, the optimal- developmental temperature hypothesis (Huey & Berrigan, 1996), the warmer is better hypothesis as well as the colder is better hypothesis (Huey et al., 1999) which compared the survival of organisms after exposure to optimal, high as well as low temperatures during some stages of their development. These hypotheses tested the mortality rates of the adults after exposure to certain temperatures and their ability to acclimatise to various temperatures ensuring survival

The aim of this experimental procedure was to determine the survival of the woodlice at a very high temperature after pre-exposure to a low and a fairly high temperature in their developmental stages.

METHODS AND MATERIALS

As per practical schedule.

RESULTS

Results of this Practical lab have been removed. They are available in the original downloadable file. Search for it here.

DISCUSSION

The exposure to high temperatures in comparison to the other woodlice population has allowed the 25oC woodlice population to attain better acclimation to the 45oC temperature due to heat resistance as noted in the lower acclimation period at the start of the experiment. This attributing to a lower mortality rate compared to the 15oC and possibly supporting the Warmer-is-better hypothesis (Huey et al., 1999) hinting that such an exposure during development may have led to adults that outperformed those bred at a lower temperature. The general trend hence shows that as the acclimation period increased, the mortality rate decreased in the 25oC woodlice population (Cossins & Bowler, 1978).

Populations exposed to low temperature may acclimatize to lower temperature areas and may not survive high temperatures thus this may have explained the high mortality rates of the woodlice bred at 15oC

An increase in the mortality rate at 9.8min in the 25 woodlice population, may have been attributed to a variation in the genetic and phenotypic make-up of the woodlice. This was a sample of a population and variation in populations differ (Cooper et al., 2010), thus some may have been accustomed to a higher temperature, whilst some at that temperature would not have acclimatized and thus did not survive.

Generally both samples of the woodlice showed a low mortality as both populations recorded a number of survivors after the experiment, and this can be attributed to the physiology of the woodlice. They generally conserve a lot of water and at high temperatures the evaporation rate from their bodies decreases and thus ensures survival (Edney, 1952).

This concludes that organisms in a population would react differently to changes in the environment, leading to some attaining acclimation methods that enhance their performance in the existing environment whilst some would succumb to the acutely introduced stresses.

REFERENCES

Bradshaw, A.D. (1965). Evolutionary significance of phenotypic plasticity in plants. Advances in Genetics, 13, 115–155.

Cooper, B. S., Czarnoleski, M., & Angilletta, M. J. (2010). Acclimation of thermal physiology in natural populations of Drosophila melanogaster: a test of an optimality model. Journal of evolutionary Biology, 23, 2346-2355.

Cossins, A. R., & Bowler, K. (1978). Temperature biology of animals. London: Chapman & Hall.

Edney, E. B. (1952). The temperature of woodlice in the sun. Zoology Department, University of Birmingham, 331-349.

Huey, R.B. & Berrigan, D. 1996. Testing evolutionary hypotheses of acclimation. In I.A. Johnston & A.F. Bennett (Ed.). Animals and Temperature: Phenotypic and Evolutionary Adaptation. (pp. 205–237). Cambridge: Cambridge University Press.

Huey, R.B., Berrigan, D., Gilchrist, G.W. & Herron, J.C. (1999). Testing the adaptive significance of acclimation: a strong inference approach. Animal. Zoology, 39, 323–336.

Karl, I., Becker, M., Hinzke, T., Mielke, M., Schiffer, M., & Fischer, K. (2014). Interactive effects of acclimation temperature and short-term stress exposure on resistance traits in the butterfly Bicyclus anynana. Physiological Entomology, 39, 222–228.

Leroi, A. M., Bennett, A. F., & Lenski, R. E. (1994). Temperature acclimation and competitive fitness: an experimental test of the beneficial acclimation assumption. Proc. Natl. Acad. Sci, 91, 1917–1921.

Pigliucci, ,M. (2001). Phenotypic Plasticity: Beyond Nature and Nurture. Maryland: Johns Hopkins University Press, Baltimore.

Prosser, C.L. (1991). Environmental and Metabolic Animal Physiology. New York: Wiley-Liss.

Wilson, R. S., & Franklin, C. E. (2000). Inability of adult Limnodynastes peronii (Amphibia : Anura) to thermally acclimate locomotory performance. Comp. Biochem. Physiol. A Mol. Integr. Physiol, 127, 21–28.

Wilson, R. S., Hammill, E., & Johnston, I.A. (2007). Competition moderates the benefits of thermal acclimation to reproductive performance in male eastern mosquito fish. Proc. Biol. Sci. 274, 1199–1204.

Yamori, W., Suzuki, K., Noguchi, K., Nakai, M., & Terashima, I. (2006). Effects of Rubisco kinetics and Rubisco activation state on the temperature dependence of the photosynthetic rate in spinach leaves from contrasting growth temperatures, Plant Cell Environ, 29, 1659–1670.

image from here

bottom of page