In angiosperms, after the floral transition, the inflorescence meristem produces floral meristems (FMs). Determinate growth of FMs produces flowers of a particular size and form. This determinate growth requires specification of floral organs and termination of stem-cell divisions. Establishment of the FM and specification of outer whorl organs (sepals and petals) requires the floral homeotic g...

Meristems may be determinate or indeterminate. In maize, the indeterminate inflorescence meristem produces three types of determinate meristems: spikelet pair, spikelet and floral meristems. These meristems are defined by their position and their products. We have discovered a gene in maize, indeterminate floral apex1 (ifa1) that regulates meristem determinacy. The defect found in ifa1 mutants ...

UNLABELLED PREMISE OF THE STUDY Pollination is a critical phase for plant reproduction, but ecological and evolutionary outcomes by pollinators may be counteracted by floral herbivores. These interacting assemblages may also be altered (directly or indirectly) by introduced species, especially on oceanic islands. In this study, we analyzed the effects of opportunistic nectar-feeding passerin...

The evolution of floral zygomorphy is an important innovation in flowering plants and is thought to arise principally from specialization on various insect pollinators. Floral morphology of neotropical Malpighiaceae is distinctive and highly conserved, especially with regard to symmetry, and is thought to be caused by selection by its oil-bee pollinators. We sought to characterize the genetic b...

Native bees provide essential pollination services to cultivated and wild plants worldwide. Despite the need to conserve pollinators, the foraging patterns of native bees are poorly understood. Classic concepts of resource use have typically categorized bee species as specialists or generalists based on floral visitation patterns. While intraspecific variation in bee foraging likely depends on ...

We present the initial phenotypic characterization of an Arabidopsis mutation, terminal flower 1-1 (tfl1-1), that identifies a new genetic locus, TFL1. The tfl1-1 mutation causes early flowering and limits the development of the normally indeterminate inflorescence by promoting the formation of a terminal floral meristem. Inflorescence development in mutant plants often terminates with a compou...

Reproductive timing is a critical life-history event that could influence the (co)variation of traits developing later in ontogeny by regulating exposure to seasonally variable factors. In a field experiment with Arabidopsis thaliana, we explore whether allelic variation at a flowering-time gene of major effect (FRIGIDA) affects (co)variation of floral traits by regulating exposure to photoperi...

Yucca moths (Tegeticula spp.) are the exclusive pollinators of Joshua trees (Yucca brevifolia s. l.). The moths actively pollinate the Joshua tree flowers and lay their eggs in the style. Recent studies have revealed that the plants commonly known as Joshua trees include two distinct, sister-species of plant: Yucca brevifolia Engelm. and Yucca jaegeriana McKelvey, each pollinated by two sister-...

Although bee-plant associations are generally maintained through speciation processes, host shifts have occurred during evolution. Understanding shifts between both phylogenetically and morphologically unrelated plants (i.e., host-saltation) is especially important since they could have been key processes in the origin and radiation of bees. Probably far from being a random process, such host-s...

Distyly, a special polymorph, has evolved in many groups of angiosperms and has attracted attention since Darwin's time. Development studies on distylous taxa have helped us to understand the evolutionary process of this polymorph, but most of these studies focus on species with narrowly tubular corolla. Here, we studied the floral development of Polygonum jucundum, a distylous species with bro...