The genetic architecture of the total phenotype may substantially constrain or enhance the evolution of floral color within populations in response to multiple selection pressures. Using Claytonia virginica I previously identified opposing selection on floral color generated through herbivores and pathogens. Here I ask whether the evolution of floral color in this system is constrained or uncon...

Developing new ornamental cultivars with improved floral attributes is a major goal in floriculture. Biotechnological approach together with classical breeding methods has been used to modify floral color, appearance as well as for increasing disease resistance. Transgenic strategies possess immense potential to produce novel flower phenotypes that are not found in nature. Adoption of Genetic e...

Floral traits and the relative contribution of autonomous selfing to total seed set varies geographically and is often driven by the availability and abundance of suitable pollinators and/or the presence of co-flowering relatives. In the latter case, competition for pollinator services and costs of hybridization can select for floral traits that reduce interspecific gene flow and contribute to ...

Recent studies clarifying the closest relatives of the world's largest flowers, Rafflesiaceae, whose floral diameters range from approximately 11 to approximately 100 cm, indicated that they evolved from tiny-flowered ancestors in a burst of floral gigantism. New data now suggest that floral size evolution within Rafflesiaceae may be more dynamic than expected, with both recent and rapid change...

In Arabidopsis, the population of stem cells present in young flower buds is lost after the production of a fixed number of floral organs. The precisely timed repression of the stem cell identity gene WUSCHEL (WUS) by the floral homeotic protein AGAMOUS (AG) is a key part of this process. In this study, we report on the identification of a novel input into the process of floral stem cell regula...

Information on floral resource costs is fundamental for understanding how selection operates on floral morphology. In this study, I explored the cost of maturing flowers in a self-incompatible population of the ligulate composite Crepis tectorum L. by experimentally manipulating floral investment and then monitoring the response in reproductive effort. Plants on which the heads were removed dur...

SEPALLATA (SEP) genes form an integral part of models that outline the molecular basis of floral organ determination and are hypothesized to act as co-factors with ABCD floral homeotic genes in specifying different floral whorls. The four SEP genes in Arabidopsis function redundantly, but the extent to which SEP genes in other flowering plants function similarly is unknown. Using a recent 113-g...

The plant MADS-box regulatory gene family includes several loci that control different aspects of inflorescence and floral development. Orthologs to the Arabidopsis thaliana MADS-box floral meristem genes APETALA1 and CAULIFLOWER and the floral organ identity genes APETALA3 and PISTILLATA were isolated from the congeneric species Arabidopsis lyrata. Analysis of these loci between these two Arab...

The strength and direction of natural selection on floral traits can vary spatially and temporally because of variation in the biotic and abiotic environment. High spatial variation in selection should lead to differentiation of floral traits among populations. In contrast, high temporal variation in selection should retard the evolution of population-specific floral phenotypes. To determine th...

calendula officinalis (family compositae) flowers are recognized as safe substance for food use by food and drug administration. present study was aimed to determine the modulatory effect of floral extracts of c. officinalis administrations on mean blood glucose (mbg), per cent glycosylated hemoglobin (hba1c), lipid profile [(total cholesterol (tc), triglycerides (tg), low and high density lipo...