In light of climate change, the ability to predict evolutionary responses to rising temperatures is of central importance for conservation efforts. Using populations of threespine sticklebacks from geothermally warmed lakes and adjacent ambient-temperature lakes in Iceland, I tested for parallel divergence in their morphology, physiology, and behaviour. Parallel evolution between populations from contrasting thermal regimes would suggest that evolutionary changes in response to elevated temperature are repeatable and predictable.


Pilakouta N, Killen SS, Kristjánsson BK, Skúlason S, Lindström J, Metcalfe NB, Parsons KJ (2019) Temperature preference does not evolve in sticklebacks despite multigenerational exposure to elevated temperatures. BioRxiv [Preprint].

Pilakouta N, Humble JL, Hill IDC, Killen SS, Kristjánsson BK, Skúlason S, Lindström J, Metcalfe NB, Parsons KJ (2019) Testing the predictability of morphological evolution in naturally warmed stickleback populations. BioRxiv [Preprint]. 

Pilakouta N, Killen SS, Kristjánsson BK, Skúlason S, Lindström J, Metcalfe NB, Parsons KJ (2020) Reduction in standard metabolic rate after multigenerational exposure to elevated temperatures in the wild. Functional Ecology (in press).


The severity of inbreeding depression can vary substantially both among and within species. This variation has been attributed to differences in the physical or social environment. I conducted a series of experiments to investigate how family interactions, such as parental care and sibling competition, affect the magnitude of inbreeding depression.


Pilakouta N, Jamieson S, Moorad JA, Smiseth PT (2015) Parental care buffers against inbreeding depression in burying beetles. Proceedings of the National Academy of Sciences 112:8031-8035.


Pilakouta N, Sieber DJ, Smiseth PT (2016) Sibling competition does not exacerbate inbreeding depression in the burying beetle Nicrophorus vespilloides. Journal of Evolutionary Biology 29:704-710.

Pilakouta N, Smiseth PT (2016) Maternal effects alter the severity of inbreeding depression in the offspring. Proceedings of the Royal Society B 20161023.


Sexual conflict arises when males and females have divergent reproductive interests. It can occur prior to mating (e.g., male harassment and female resistance), during mating (e.g., duration of copulation), or after offspring have hatched or been born (e.g., contribution to parental care by each sex). I examined sexual conflict over parental care and consumption of a shared breeding resource, using small and large males and females to introduce variation in the parents' quality.


Pilakouta N, Richardson J, Smiseth PT (2015) State-dependent cooperation in burying beetles: parents adjust their contribution towards care based on both their own and their partner’s size. Journal of Evolutionary Biology 28:1965-1974.


Pilakouta N, Richardson J, Smiseth PT (2016) If you eat, I eat: resolution of sexual conflict over consumption from a shared resource. Animal Behaviour 111:175-180.


Females typically prefer conspicuous males but tend to reverse this preference in the presence of predators because of a higher risk of predation due to associating with conspicuous males. I investigated (i) how long this reversal in mating preferences persists after exposure to a predator and (ii) whether females might choose an inconspicuous heterospecific male over a conspicuous conspecific male when there is a high risk of predation.


Pilakouta N, Alonzo SH (2014) Predator exposure leads to a short-term reversal in female mate preferences in the green swordtail, Xiphophorus helleri. Behavioral Ecology 25:306-312.


Pilakouta N, Correa MA, Alonzo SH (2017) Predation risk reduces a female preference for heterospecific males in the green swordtail. Ethology 123:95-104.

Zoology Building, University of Aberdeen, UK

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