Tests for the joint evolution of mating system and drought escape in Mimulus - PubMed Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2012 Feb;109(3):583-98.
doi: 10.1093/aob/mcr160. Epub 2011 Aug 10.

Tests for the joint evolution of mating system and drought escape in Mimulus

Affiliations
Comparative Study

Tests for the joint evolution of mating system and drought escape in Mimulus

Christopher T Ivey et al. Ann Bot. 2012 Feb.

Erratum in

  • Ann Bot. 2012 Jun;109(7):1381

Abstract

Background and aims: Self-fertilizing taxa are often found at the range margins of their progenitors, where sub-optimal habitats may select for alternative physiological strategies. The extent to which self-fertilization is favoured directly vs. arising indirectly through correlations with other adaptive life history traits is unclear. Trait responses to selection depend on genetic variation and covariation, as well as phenotypic and genetic responses to altered environmental conditions. We tested predictions of the hypothesis that self-fertilization in Mimulus arises through direct selection on physiological and developmental traits that allow seasonal drought escape.

Methods: Phenotypic selection on mating system and drought escape traits was estimated in field populations of M. guttatus. In addition, trait phenotype and phenotypic selection were compared between experimental wet and dry soil in two greenhouse populations each of M. guttatus and M. nasutus. Finally, genetic variation and covariation for traits were compared between wet and dry soil treatments in a greenhouse population of M. guttatus.

Key results: Consistent with predictions, selection for early flowering was generally stronger than for mating system traits, and selection for early flowering was stronger in dry soil. Inconsistent with predictions, selection for water-use efficiency was largely absent; selection for large flowers was stronger than for drought escape in the field; and most drought escape and mating system traits were not genetically correlated. A positive genetic correlation between flowering time and flower size, which opposed the adaptive contour, emerged only in wet soil, suggesting that variation in water availability may maintain variation in these traits. Plastic responses to soil moisture treatments supported the idea that taxonomic divergence could have been facilitated by plasticity in flowering time and selfing.

Conclusions: The hypothesis that plant mating systems may evolve indirectly via selection on correlated life history characteristics is plausible and warrants increased attention.

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
Means (±s.d.) of flower size (A), anther–stigma separation (B), Julian date of first flower (C), leaf %N content (D), leaf 13C isotope ratio (E), lifetime seed set (F) and above-ground biomass (G) in two field populations of flowering Mimulus guttatus in Lassen National Forest, Butte County, California, USA.
Fig. 2.
Fig. 2.
Least-squares means (±s.e.) of flower size (A), anther–stigma separation (B), days from sowing to first flower (C), leaf %N content (D), leaf 13C isotope ratio (E), number of flowers produced (F) and above-ground biomass (G) in greenhouse populations of Mimulus guttatus (CCR and DRC) and M. nasutus (COH and HON) grown in experimentally dry and wet soil, as indicated. P < 0·1, *P < 0·05, **P < 0·01, ***P < 0·001, ****P < 0·0001 in mixed-model ANOVA comparisons of trait means between treatments within populations.
Fig. 3.
Fig. 3.
Least-squares means (±s.e.) of flower size (A), anther–stigma separation (B), days from sowing to first flower (C), leaf %N content (D), leaf 13C isotope ratio (E), number of flowers produced (F) and above-ground biomass (G) in a greenhouse population of Mimulus guttatus grown in experimentally dry and wet soil. **P < 0·01, ****P < 0·0001 in mixed-model ANOVA comparisons of trait means between treatments.

Similar articles

Cited by

References

    1. Angert AL. Growth and leaf physiology of monkeyflowers with different altitude ranges. Oecologia. 2006;148:183–194. - PubMed
    1. Armbruster WS, Mulder CPH, Baldwin BG, Kalisz S, Wessa B, Nute H. Comparative analysis of late floral development and mating-system evolution in tribe Collinsieae (Scrophulariacae) American Journal of Botany. 2002;89:37–49. - PubMed
    1. Arntz AM, Delph LF. Pattern and process: evidence for the evolution of photosynthetic traits in natural populations. Oecologia. 2001;127:455–467. - PubMed
    1. Arntz AM, DeLucia EH, Jordan N. Fitness effects of a photosynthetic mutation across contrasting environments. Journal of Evolutionary Biology. 2000;13:792–803.
    1. Arroyo MTK. Chiasma frequency evidence on the evolution of autogamy in Limnanthes floccosa (Limnanthaceae) Evolution. 1973;27:679–688. - PubMed

Publication types