Daphnia as a Model for Eco-evolutionary Dynamics

2018 ◽  
pp. 403-424
Author(s):  
Matthew R. Walsh ◽  
Michelle Packer ◽  
Shannon Beston ◽  
Collin Funkhouser ◽  
Michael Gillis ◽  
...  

Much research has shown that variation in ecological processes can drive rapid evolutionary changes over periods of years to decades. Such contemporary adaptation sets the stage for evolution to have reciprocal impacts on the properties of populations, communities, and ecosystems, with ongoing interactions between ecological and evolutionary forces. The importance and generality of these eco-evolutionary dynamics are largely unknown. In this chapter, we promote the use of water fleas (Daphnia sp.) as a model organism in the exploration of eco-evolutionary interactions in nature. The many characteristics of Daphnia that make them suitable for laboratory study in conjunction with their well-known ecological importance in lakes, position Daphnia to contribute new and important insights into eco-evolutionary dynamics. We first review the influence of key environmental stressors in Daphnia evolution. We then highlight recent work documenting the pathway from life history evolution to ecology using Daphnia as a model. This review demonstrates that much is known about the influence of ecology on Daphnia life history evolution, while research exploring the genomic basis of adaptation as well as the influence of Daphnia life history traits on ecological processes is beginning to accumulate.

2017 ◽  
Author(s):  
Todd L. Parsons ◽  
Amaury Lambert ◽  
Troy Day ◽  
Sylvain Gandon

AbstractThe theory of life history evolution provides a powerful framework to understand the evolutionary dynamics of pathogens in both epidemic and endemic situations. This framework, however, relies on the assumption that pathogen populations are very large and that one can neglect the effects of demographic stochasticity. Here we expand the theory of life history evolution to account for the effects of finite population size on the evolution of pathogen virulence. We show that demographic stochasticity introduces additional evolutionary forces that can qualitatively affect the dynamics and the evolutionary outcome. We discuss the importance of the shape of pathogen fitness landscape and host heterogeneity on the balance between mutation, selection and genetic drift. In particular, we discuss scenarios where finite population size can dramatically affect classical predictions of deterministic models. This analysis reconciles Adaptive Dynamics with population genetics in finite populations and thus provides a new theoretical toolbox to study life-history evolution in realistic ecological scenarios.


2018 ◽  
Vol 15 (147) ◽  
pp. 20180135 ◽  
Author(s):  
Todd L. Parsons ◽  
Amaury Lambert ◽  
Troy Day ◽  
Sylvain Gandon

The theory of life-history evolution provides a powerful framework to understand the evolutionary dynamics of pathogens. It assumes, however, that host populations are large and that one can neglect the effects of demographic stochasticity. Here, we expand the theory to account for the effects of finite population size on the evolution of pathogen virulence. We show that demographic stochasticity introduces additional evolutionary forces that can qualitatively affect the dynamics and the evolutionary outcome. We discuss the importance of the shape of the pathogen fitness landscape on the balance between mutation, selection and genetic drift. This analysis reconciles Adaptive Dynamics with population genetics in finite populations and provides a new theoretical toolbox to study life-history evolution in realistic ecological scenarios.


2016 ◽  
Vol 113 (52) ◽  
pp. 15030-15035 ◽  
Author(s):  
Anne Maria Eikeset ◽  
Erin S. Dunlop ◽  
Mikko Heino ◽  
Geir Storvik ◽  
Nils C. Stenseth ◽  
...  

The relative roles of density dependence and life history evolution in contributing to rapid fisheries-induced trait changes remain debated. In the 1930s, northeast Arctic cod (Gadus morhua), currently the world’s largest cod stock, experienced a shift from a traditional spawning-ground fishery to an industrial trawl fishery with elevated exploitation in the stock’s feeding grounds. Since then, age and length at maturation have declined dramatically, a trend paralleled in other exploited stocks worldwide. These trends can be explained by demographic truncation of the population’s age structure, phenotypic plasticity in maturation arising through density-dependent growth, fisheries-induced evolution favoring faster-growing or earlier-maturing fish, or a combination of these processes. Here, we use a multitrait eco-evolutionary model to assess the capacity of these processes to reproduce 74 y of historical data on age and length at maturation in northeast Arctic cod, while mimicking the stock’s historical harvesting regime. Our results show that model predictions critically depend on the assumed density dependence of growth: when this is weak, life history evolution might be necessary to prevent stock collapse, whereas when a stronger density dependence estimated from recent data is used, the role of evolution in explaining fisheries-induced trait changes is diminished. Our integrative analysis of density-dependent growth, multitrait evolution, and stock-specific time series data underscores the importance of jointly considering evolutionary and ecological processes, enabling a more comprehensive perspective on empirically observed stock dynamics than previous studies could provide.


2008 ◽  
Vol 105 (40) ◽  
pp. 15475-15480 ◽  
Author(s):  
Fabrice Duponchelle ◽  
Emmanuel Paradis ◽  
Anthony J. Ribbink ◽  
George F. Turner

The existence of ancient deep-water lakes provides an opportunity to study the independent adaptation of aquatic organisms to pelagic, benthic, and rocky shore habitats. With improving resolution of their phylogenetic relationships, the many cichlid fish species endemic to the African Great Lakes Malawi, Tanganyika, and Victoria provide a significant resource for the comparative study of such evolutionary processes. Here, we show that cichlid lineages colonizing rocky shores and pelagic habitats in the different lakes have independently evolved larger eggs and lower fecundities than benthic lineages, suggesting parallel adaptive life-history evolution. By contrast, other pelagic teleost fishes in both marine and freshwater habitats, including African lakes, typically produce large numbers of very small eggs. Our results also suggest that decreased fecundity and increased egg size not only occurred independently in each lake but occurred independently in the colonization of rocky and pelagic habitats.


2015 ◽  
Author(s):  
Katrien Van Petegem ◽  
Jeroen Boeye ◽  
Robby Stoks ◽  
Dries Bonte

In the context of climate change and species invasions, range shifts increasingly gain attention because the rates at which they occur in the Anthropocene induce fast shifts in biological assemblages. During such range shifts, species experience multiple selection pressures. Especially for poleward expansions, a straightforward interpretation of the observed evolutionary dynamics is hampered because of the joint action of evolutionary processes related to spatial selection and to adaptation towards local climatic conditions. To disentangle the effects of these two processes, we integrated stochastic modeling and empirical approaches, using the spider mite Tetranychus urticae as a model species. We demonstrate considerable latitudinal quantitative genetic divergence in life-history traits in T. urticae, that was shaped by both spatial selection and local adaptation. The former mainly affected dispersal behavior, while development was mainly shaped by adaptation to the local climate. Divergence in life-history traits in species shifting their range poleward can consequently be jointly determined by fast local adaptation to the environmental gradient and contemporary evolutionary dynamics resulting from spatial selection. The integration of modeling with common garden experiments provides a powerful tool to study the contribution of these two evolutionary processes on life-history evolution during range expansion.


2017 ◽  
Author(s):  
Dries Bonte ◽  
Quinten Bafort

1. The spatial configuration and size of patches influence metapopulation dynamics by altering colonisation-extinction dynamics and local density-dependency. This spatial forcing as determined by the metapopulation typology then imposes strong selection pressures on life history traits, which will in turn feedback on the ecological metapopulation dynamics. Given the relevance of metapopulation persistence for biological conservation, and the potential rescuing role of evolution, a firm understanding of the relevance of these eco-evolutionary processes is essential. 2. We here follow a systems modelling approach to quantify the importance of spatial forcing and experimentally observed life history evolution for metapopulation demography as quantified by (meta)population size and variability. We therefore developed an individual based model matching an earlier experimental evolution with spider mites to perform virtual translocation and invasion experiments that would have been otherwise impossible to conduct. 3. We show that (1) metapopulation demography is more affected by spatial forcing than by life history evolution, but that life history evolution contributes substantially to changes in local and especially metapopulation-level population sizes, (2) extinction rates are minimised by evolution in classical metapopulations, and (3) evolution is optimising individual performance in metapopulations when considering the importance of more cryptic stress resistance evolution. 4. Ecological systems modelling opens up a promising avenue to quantify the importance of eco-evolutionary feedbacks for larger-scale population dynamics. Metapopulation sizes are especially impacted by evolution but its variability is mainly determined by the spatial forcing. 5. Eco-evolutionary dynamics can increase the persistence of classical metapopulations. The maintenance of evolutionary dynamics in spatially structured populations is thus not only essential in the face of environmental change; it also generates feedbacks that impact metapopulation persistence.


2010 ◽  
Vol 59 (5) ◽  
pp. 504-517 ◽  
Author(s):  
Jonathan M. Waters ◽  
Diane L. Rowe ◽  
Christopher P. Burridge ◽  
Graham P. Wallis

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