Bet-Hedging Germination of Desert Annuals: Variation Among Populations and Maternal Effects in Lepidium lasiocarpum

1993 ◽  
Vol 142 (3) ◽  
pp. 488-507 ◽  
Author(s):  
Thomas Philippi
1993 ◽  
Vol 142 (3) ◽  
pp. 474-487 ◽  
Author(s):  
Thomas Philippi

2015 ◽  
Author(s):  
Snigdhadip Dey ◽  
Steve Proulx ◽  
Henrique Teotonio

Most organisms live in ever-challenging temporally fluctuating environments. Theory suggests that the evolution of anticipatory (or deterministic) maternal effects underlies adaptation to environments that regularly fluctuate every other generation because of selection for increased offspring performance. Evolution of maternal bet-hedging reproductive strategies that randomize offspring phenotypes is in turn expected to underlie adaptation to irregularly fluctuating environments. Although maternal effects are ubiquitous their adaptive significance is unknown since they can easily evolve as a correlated response to selection for increased maternal performance. Using the nematode Caenorhabditis elegans, we show the experimental evolution of maternal provisioning of offspring with glycogen, in populations facing a novel anoxia hatching environment every other generation. As expected with the evolution of deterministic maternal effects, improved embryo hatching survival under anoxia evolved at the expense of fecundity and glycogen provisioning when mothers experienced anoxia early in life. Unexpectedly, populations facing an irregularly fluctuating anoxia hatching environment failed to evolve maternal bet-hedging reproductive strategies. Instead, adaptation in these populations should have occurred through the evolution of balancing trade-offs over multiple generations, since they evolved reduced fitness over successive generations in anoxia but did not go extinct during experimental evolution. Mathematical modelling confirms our conclusion that adaptation to a wide range of patterns of environmental fluctuations hinges on the existence of deterministic maternal effects, and that they are generally much more likely to contribute to adaptation than maternal bet-hedging reproductive strategies.


2015 ◽  
Author(s):  
Stephen R Proulx ◽  
Henrique Teotonio

Adaptation to temporally fluctuating environments can be achieved through direct phenotypic evolution, by phenotypic plasticity (either developmental plasticity or trans-generational plasticity), or by randomizing offspring phenotypes (often called diversifying bet-hedging). Theory has long held that plasticity can evolve when information about the future environment is reliable while bet-hedging can evolve when mixtures of phenotypes have high average fitness (leading to low among generation variance in fitness). To date, no study has studied the evolutionary routes that lead to the evolution of randomized offspring phenotypes on the one hand or deterministic maternal effects on the other. We develop simple, yet general, models of the evolution of maternal effects and are able to directly compare selection for deterministic and randomizing maternal effects and can also incorporate the notion of differential maternal costs of producing offspring with alternative phenotypes. We find that only a small set of parameters allow bet hedging type strategies to outcompete deterministic maternal effects. Not only must there be little or no informative cues available, but also the frequency with which different environments are present must fall within a narrow range. By contrast, when we consider the joint evolution of the maternal strategy and the set of offspring phenotypes we find that deterministic maternal effects can always invade the ancestral state (lacking any form of maternal effect). The long-term ESS may, however, involve some form of offspring randomization, but only if the phenotypes evolve extreme differences in environment-specific fitness. Overall we conclude that deterministic maternal effects are much more likely to evolve than offspring randomization, and offspring randomization will only be maintained if it results in extreme differences in environment-specific fitness.


2000 ◽  
Vol 155 (2) ◽  
pp. 168-186 ◽  
Author(s):  
M. J. Clauss ◽  
D. L. Venable

Ecology ◽  
2007 ◽  
Vol 88 (5) ◽  
pp. 1086-1090 ◽  
Author(s):  
D. Lawrence Venable
Keyword(s):  

2019 ◽  
Vol 29 (2) ◽  
pp. 149-153 ◽  
Author(s):  
Li Jiang ◽  
Lei Wang ◽  
Carol C. Baskin ◽  
Changyan Tian ◽  
Zhenying Huang

AbstractMaternal effects on offspring seeds are mainly caused by seed position on, and the abiotic environment of, the mother plant. Seed heteromorphism, a special form of position effect, is the production by an individual plant of morphologically distinct seed types, usually with different ecological behaviours. Seed heteromorphism is assumed to be a form of bet hedging and provides an ideal biological model to test theoretical predictions. Most studies of maternal effects on seeds have focused on abiotic environmental factors and changes in mean seed traits of offspring. Suaeda salsa is an annual halophyte that produces dimorphic seeds within the same inflorescence. We tested the hypothesis that plants grown from brown seeds of S. salsa have a higher offspring brown seed:black seed morph ratio and variance in seed size than plants from black seeds. Results from a pot experiment showed that plants grown from brown seeds had a higher brown seed:black seed ratio than plants grown from black seeds. This is the first layer of dynamic bet hedging. Brown seeds had higher size variation than black seeds, and seeds produced by plants from brown seeds also had higher seed size variation than plants grown from black seeds. This is the second layer of dynamic bet hedging. Thus, the maternal effect of seed heteromorphism is dual dynamic bet hedging. Furthermore, for seed traits we verified for the first time the theoretical prediction that an increase in offspring size variability induces an increase in the mean size of offspring.


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