Moonlight pollination in the gymnosperm Ephedra

Most gymnosperms are wind-pollinated, but some are insect-pollinated, and in Ephedra (Gnetales), both wind pollination and insect pollination occur. Little is, however, known about mechanisms and evolution of pollination syndromes in gymnosperms. Based on four seasons of field studies, we show an unexpected correlation between pollination and the phases of the moon in one of our studied species, Ephedra foeminea. It is pollinated by dipterans and lepidopterans, most of them nocturnal, and its pollination coincides with the full moon of July. This may be adaptive in two ways. Many nocturnal insects navigate using the moon. Further, the spectacular reflection of the full-moonlight in the pollination drops is the only apparent means of nocturnal attraction of insects in these plants. In the sympatric but wind-pollinated Ephedra distachya, pollination is not correlated to the full moon but occurs at approximately the same dates every year. The lunar correlation has probably been lost in most species of Ephedra subsequent an evolutionary shift to wind pollination in the clade. When the services of insects are no longer needed for successful pollination, the adaptive value of correlating pollination with the full moon is lost, and conceivably also the trait

Degradome and Secretome of Pollination Drops of Ephedra

Although secreted proteins (a secretome) are known to occur in gymnosperm pollination drops, this study shows evidence for the presence of a protein degradome for the first time. A protein degradome is composed of protein and peptide fragments, a product of protein breakdown, whereas a secretome is composed of whole, secreted, and often biologically active extracellular proteins. Harvested Ephedra pollination drops from seven species were pooled either by collection date or, in the case of less abundant sample volumes, by species. Samples were processed by one of two methods: 1. gel electophoresis or by 2. liquid-liquid extraction, followed by chromatographic separation. Processed samples were trypsin-digested and analyzed with a Thermo Scientific LTQ Orbitrap Velos. On average, two-thirds of the detected and characterized proteins found in Ephedra spp. pollination drops were intracellular proteins, such as ubiquitin. The remaining third represent proteins known to be secreted, often involved in apoplastic processes such as defense and carbohydrate-modification, typical of known conifer pollination drop proteins. Characterized proteins detected in our comparative study of Ephedra spp drops ranged from 6 in E. monosperma to 20 in E. foeminea. We propose that the intracellular proteins detected are present as the result of nucellar tissue degeneration during pollination drop formation; previous proteomic investigations of pollination drops were in taxa that lack nucellar degeneration during drop formation Discovery of a degradome in pollination drops is novel and significant in that its presence has biological implications for pollination biology. We predict that degradomes in pollination drops are not restricted to Ephedra, but should also occur in species with nucellar tissue breakdown that coincides with pollination drop formation, such as in cycads and Ginkgo and some Pinaceae. Analysis of several collection dates of E. monosperma shows a large number of proteins that change over the course of the pollination drop secretion period, which suggests that variation in pollination drop contents over time may be important in the pollination biology of Ephdera.The authors would like to thank University of Victoria (UVic), UVic-Genome BC Proteomics Centre (UVic-GBCP), Genome Canada, and Genome BC for their support, as well as the Natural Sciences and Engineering Research Council of Canada (NSERC) for a Discovery Research Grant Program (PvA), and a Postgraduate Scholarship Program Grant (NAP). We acknowledge the expert assistance of B. Gowen (UVic), D. Smith (UVic) and Dr. Carol Parker (UVic-GBCP), as well as the invaluable assistance in sample collections from S. Ickert-Bond, C. Rydin, K. Bolinder, A. Rydberg, J. Jernstedt and I. Loera-Carrizales.FacultyReviewe