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Constrained flexibility of parental cooperation limits adaptive responses to harsh conditions.

ABSTRACT: Parental care is predicted to evolve to mitigate harsh environments, thus adaptive plasticity of care may be an important response to our climate crisis. In biparental species, fitness costs may be reduced by resolving conflict and enhancing cooperation among partners. We investigated this prediction with the burying beetle, Nicrophorus orbicollis, by exposing them to contrasting benign and harsh thermal environments. Despite measurable fitness costs under the harsh environment, sexual conflict persisted in the form of sex-specific social plasticity. That is, females provided equivalent care with or without males, whereas males with partners deserted earlier and reduced provisioning effort. The interaction of social condition and thermal environment did not explain variation in individual behavior, failing to support a temperature-mediated shift from conflict to cooperation. Examining selection gradients and splines on cumulative care revealed a likely explanation for these patterns. Contrary to predictions, increased care did not enhance offspring performance under stress. Rather, different components of care were under different selection regimes, with optimization constrained due to lack of coordination between parents. We suggest that the potential for parenting to ameliorate the effects of our climate crisis may depend on the sex-specific evolutionary drivers of parental care, and that this may be best reflected in components of care.

SUBMITTER: Moss JB

PROVIDER: S-EPMC8362138 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Background and objectivesPhenotypic plasticity enables organisms to maximize fitness by matching trait values to different environments. Such adaptive phenotypic plasticity is exhibited by parasites, which experience frequent environmental changes during their life cycle, between individual hosts and also in within-host conditions experienced during infections. Life history theory predicts that the evolution of adaptive phenotypic plasticity is limited by costs and constraints, but tests of these concepts are scarce.MethodologyHere, we induce phenotypic plasticity in malaria parasites to test whether mounting a plastic response to an environmental perturbation constrains subsequent plastic responses to further environmental change. Specifically, we perturb red blood cell resource availability to induce Plasmodium chabaudi to alter the trait values of several phenotypes underpinning within-host replication and between-host transmission. We then transfer parasites to unperturbed hosts to examine whether constraints govern the parasites' ability to alter these phenotypes in response to their new in-host environment.ResultsParasites alter trait values in response to the within-host environment they are exposed to. We do not detect negative consequences, for within-host replication or between-host transmission, of previously mounting a plastic response to a perturbed within-host environment.Conclusions and implicationsWe suggest that malaria parasites are highly plastic and adapted to adjusting their phenotypes in response to the frequent changes in the within-host conditions they experience during infections. Our findings support the growing body of evidence that medical interventions, such as anti-parasite drugs, induce plastic responses that are adaptive and can facilitate the survival and potentially, drug resistance of parasites.Lay summaryMalaria parasites have evolved flexible strategies to cope with the changing conditions they experience during infections. We show that using such flexible strategies does not impact upon the parasites' ability to grow (resulting in disease symptoms) or transmit (spreading the disease).

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Constrained flexibility of parental cooperation limits adaptive responses to harsh conditions.

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