scholarly journals Predicting the effects of nectar robbing on plant reproduction: implications of pollen limitation and plant mating system

2007 ◽  
Vol 94 (12) ◽  
pp. 1935-1943 ◽  
Author(s):  
Laura A. Burkle ◽  
Rebecca E. Irwin ◽  
Daniel A. Newman
2021 ◽  
Author(s):  
Rianne E Fernandes ◽  
Melissa A Millar ◽  
David J Coates ◽  
Margaret Byrne ◽  
Siegfried L Krauss ◽  
...  

2015 ◽  
Vol 18 (7) ◽  
pp. 706-713 ◽  
Author(s):  
Dena Grossenbacher ◽  
Ryan Briscoe Runquist ◽  
Emma E. Goldberg ◽  
Yaniv Brandvain

2015 ◽  
Vol 103 (1) ◽  
pp. 110-117 ◽  
Author(s):  
Dena Grossenbacher ◽  
Ryan D. Briscoe Runquist ◽  
Emma E. Goldberg ◽  
Yaniv Brandvain

PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e10698
Author(s):  
Vania Jiménez-Lobato ◽  
Juan Núñez-Farfán

Plant mating system determines, to a great extent, the demographic and genetic properties of populations, hence their potential for adaptive evolution. Variation in plant mating system has been documented between phylogenetically related species as well between populations of a species. A common evolutionary transition, from outcrossing to selfing, is likely to occur under environmental spatial variation in the service of pollinators. Here, we studied two phenotypically (in floral traits) and genetically (in neutral molecular markers) differentiated populations of the annual, insect-pollinated, plant Datura inoxia in Mexico, that differ in the service of pollinators (Mapimí and Cañada Moreno). First, we determined the populations’ parameters of phenotypic in herkogamy, outcrossing and selfing rates with microsatellite loci, and assessed between generation (adults and seedlings) inbreeding, and inbreeding depression. Second, we compared the relationships between parameters in each population. Results point strong differences between populations: plants in Mapimí have, on average, approach herkogamy, higher outcrossing rate (tm = 0.68), lower primary selfing rate (r = 0.35), and lower inbreeding at equilibrium (Fe = 0.24) and higher inbreeding depression (δ = 0.25), than the populations of Cañada. Outcrossing seems to be favored in Mapimí while selfing in Cañada. The relationship between r and Fe were negatively associated with herkogamy in Mapimí; here, progenies derived from plants with no herkogamy or reverse herkogamy had higher selfing rate and inbreeding coefficient than plants with approach herkogamy. The difference Fe–F is positively related to primary selfing rate (r) only in Cañada Moreno which suggests inbreeding depression in selfing individuals and then genetic purging. In conclusion, mating system evolution may occur differentially among maternal lineages within populations of Datura inoxia, in which approach herkogamy favors higher outcrossing rates and low levels of inbreeding and inbreeding depression, while no herkogamy or reverse herkogamy lead to the evolution of the “selfing syndrome” following the purge of deleterious alleles despite high inbreeding among individuals.


Oikos ◽  
2016 ◽  
Vol 125 (11) ◽  
pp. 1668-1676 ◽  
Author(s):  
Jenny A. Hazlehurst ◽  
Jordan O. Karubian

2020 ◽  
Vol 51 (1) ◽  
pp. 319-340
Author(s):  
Amanda D. Benoit ◽  
Susan Kalisz

Plants are the foundation of the food web and therefore interact directly and indirectly with myriad organisms at higher trophic levels. They directly provide nourishment to mutualistic and antagonistic primary consumers (e.g., pollinators and herbivores), which in turn are consumed by predators. These interactions produce cascading indirect effects on plants (either trait-mediated or density-mediated). We review how predators affect plant-pollinator interactions and thus how predators indirectly affect plant reproduction, fitness, mating systems, and trait evolution. Predators can influence pollinator abundance and foraging behavior. In many cases, predators cause pollinators to visit plants less frequently and for shorter durations. This decline in visitation can lead to pollen limitation and decreased seed set. However, alternative outcomes can result due to differences in predator, pollinator, and plant functional traits as well as due to altered interaction networks with plant enemies. Furthermore, predators may indirectly affect the evolution of plant traits and mating systems.


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