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Sexual System (sexual + system)
Selected AbstractsLIFE-HISTORY DIFFERENTIATION AND THE MAINTENANCE OF MONOECY AND DIOECY IN SAGITTARIA LATIFOLIA (ALISMATACEAE)EVOLUTION, Issue 9 2003Marcel E. Dorken Abstract The existence of monoecious and dioecious populations within plant species is rare. This limits opportunities to investigate the ecological mechanisms responsible for the evolution and maintenance of these contrasting sexual systems. In Sagittaria latifolia, an aquatic flowering plant, monoecious and dioecious populations exist in close geographic proximity but occupy distinct wetland habitats differing in the relative importance of disturbance and competition, respectively. Life-history theory predicts contrasting evolutionary responses to these environmental conditions. We propose that the maintenance of monoecy and dioecy in S. latifolia is governed by ecological selection of divergent life-history strategies in contrasting habitats. Here we evaluate this hypothesis by comparing components of growth and reproduction between monoecious and dioecious populations under four conditions: natural populations, a uniform glasshouse environment, a common garden in which monoecious and dioecious populations and their F1 progeny were compared, and a transplant experiment using shaded and unshaded plots in a freshwater marsh. Plants from dioecious populations were larger in size and produced heavier corms in comparison with monoecious populations. Monoecious populations flowered earlier and produced more flowers, clonal ramets, and corms than dioecious populations. The life-history differences between the sexual systems were shown to have a quantitative genetic basis, with F1 progeny generally exhibiting intermediate trait values. Survival was highest for each sexual system in field plots that most closely resembled the habitats in which monoecious (unshaded) and dioecious (shaded) populations grow. These results demonstrate that monoecious and dioecious populations exhibit contrasting patterns of investment in traits involved with growth and reproduction. Selection for divergent life histories between monoecious and dioecious populations of S. latifolia appears to be the principal mechanism maintaining the integrity of the two sexual systems in areas of geographic overlap. [source] Experimental evolution with yeastFEMS YEAST RESEARCH, Issue 5 2006Clifford Zeyl Abstract Many of the difficulties of studying evolution in action can be surmounted using populations of microorganisms, such as yeast. A readily manipulated sexual system and an increasingly sophisticated array of molecular and genomic tools uniquely qualify Saccharomyces cerevisiae as an experimental subject. This minireview briefly describes some recent contributions of yeast experiments to current understanding of the evolution of ploidy, sex, mutation, and speciation. [source] Hauling Down the Double Standard: Feminism, Social Purity and Sexual Science in Late Nineteenth-Century BritainGENDER & HISTORY, Issue 1 2004Lesley Hall Nineteenth-century feminism and the related social purity movement, and the emergent scientific discourse of ,sexology', are usually seen as antagonistic. Both trends, in fact, were in profound opposition to the widespread assumption that the double moral standard was an embodiment of ,natural' transhistorical law. This article suggests that feminist agitation against the Contagious Diseases Acts of the 1860s (and other manifestations of the deleterious legal status of women) overtly attacked unthinking social assumptions about sex and gender, destabilising concepts about the naturalness of the existing sexual system and creating the context for the pioneers of sexology to interrogate even further accepted notions of gender and sexuality. [source] Linnaeus' sexual system and flowering plant phylogenyNORDIC JOURNAL OF BOTANY, Issue 1-2 2007Birgitta Bremer Carl Linnaeus brought order to the knowledge of plants and animals by arranging all known species in encyclopaedic works. He proposed a system of plants, the sexual system, based on the number and arrangement of male and female organs. His artificial sexual system has since long been replaced by ,natural' or phylogenetic systems but there has never been a comprehensive comparison of the sexual system with modern plant classification. The currently most often used classification of flowering plants is the APG-system. It is based on comprehensive phylogenies of flowering plants, reconstructed by analyses of DNA data. The APG-system covers all flowering plants which are classified in 453 families and these are classified in 45 orders. Most of the species were not known at time of Linnaeus. Families and orders in the APG-system are arranged in larger informal groups representing major branches in the flowering plant phylogenetic tree. Three such groups are the monocots, the rosids, and the asterids. I have examined all genera published in Species plantarum (1753) and classified them according to order and major groups in the APG-system. All classes except one, number 15 Tetradynamia, comprises groups of unrelated plants. Not surprisingly, the sexual system does not display what we know today about plant relationships. As is evident from this analysis, there is little correspondence between the sexual system and the APG-system. This does not mean that the sexual system has been useless or misleading. When it was introduced, it formed the basis for much intensified research and increased knowledge of plants. [source] Cryptic self-incompatibility and distyly in Hedyotis acutangula Champ. (Rubiaceae)PLANT BIOLOGY, Issue 3 2010X. Wu Abstract Distyly, floral polymorphism frequently associated with reciprocal herkogamy, self- and intramorph incompatibility and secondary dimorphism, constitutes an important sexual system in the Rubiaceae. Here we report an unusual kind of distyly associated with self- and/or intramorph compatibility in a perennial herb, Hedyotis acutangula. Floral morphology, ancillary dimorphisms and compatibility of the two morphs were studied. H. acutangula did not exhibit precise reciprocal herkogamy, but this did not affect the equality of floral morphs in the population, as usually found in distylous plants. Both pin and thrum pollen retained relatively high viability for 8 h. The pollen to ovule ratio was 72.5 in pin flowers and 54.4 in thrum flowers. Pistils of pin flowers remained receptive for longer than those of thrum flowers. No apparent difference in the germination rate of pin and thrum pollen grains was observed when cultured in vitro, although growth of thrum pollen tubes was much faster than that of pin pollen tubes. Artificial pollination revealed that pollen tube growth in legitimate intermorph crosses was faster than in either intramorph crosses or self-pollination, suggesting the occurrence of cryptic self-incompatibility in this species. Cryptic self-incompatibility functioned differently in the two morphs, with pollen tube growth rates after legitimate and illegitimate pollination much more highly differentiated in pin flowers than in thrum flowers. No fruit was produced in emasculated netted flowers, suggesting the absence of apomixis. Our results indicate that H. acutangula is distylous, with a cryptic self-incompatibility breeding system. [source] Polyploidy and the sexual system: what can we learn from Mercurialis annua?BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 4 2004JOHN R. PANNELL The evolutionary success of polyploidy most directly requires the ability of polyploid individuals to reproduce and transmit their genes to subsequent generations. As a result, the sexual system (i.e. the mating system and the sex allocation of a species) will necessarily play a key role in determining the fate of a new polyploid lineage. The effects of the sexual system on the evolution of polyploidy are complex and interactive. They include both aspects of the genetic system, the genetic load maintained in a population and the ecological context in which selection takes place. Here, we explore these complexities and review the empirical evidence for several potentially important genetic and ecological interactions between ploidy and the sexual system in plants. We place particular emphasis on work in our laboratory on the European annual plant Mercurialis annua, which offers promising scope for detailed investigations on this topic. M. annua forms a polyploid complex that varies in its sexual system from dioecy (separate sexes) through androdioecy (males and hermaphrodites) to functional hermaphroditism. © 2004 The Linnean Society of London, Biological Journal of the Linnean Society, 2004, 82, 547,560. [source] Floral phenology and sex expression in functionally monoecious Rhoiptelea chiliantha (Rhoipteleaceae)BOTANICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 2 2006SHI-GUO SUN The reproductive ecology of wind-pollinated gynomonoecious species, in which the individual plant produces both female (pistillate) and perfect flowers, has rarely been studied. We examined the floral phenology and reproductive traits in Rhoiptelea chiliantha, described as gynomonoecy, to understand the adaptive significance of this sexual system. This species is a rare tree native to south-western China and northern Vietnam. The flowers are characterized by an anemophilous pollination syndrome, but no insects were observed foraging on them. Perfect flowers have larger tepals but smaller stigmas than female flowers, indicating flower size dimorphism. Floral ratios of female to perfect flowers are stable in different individuals and populations. On individual plants, perfect flowers open first, followed by female flowers, with a 1-week interval. Perfect flowers are protogynous with a 3.7-day interval (neuter phase) between the female phase (1.5 days) and expanded male phase (8.2 days). Both female and perfect flowers exhibit pronounced synchrony in flowering at the levels of inflorescences and individuals. However, flowers on different individuals show asynchronicity in timing of initial blooming. Tracking the process from pollination to fruit maturation, we found that female flowers contributed almost exclusively to seed production, but perfect flowers were sterile (functionally males). Therefore, this plant is functionally monoecious. This finding resolved a puzzle on the occurrence of female flowers in this plant, because previous reports described female flowers as being sterile. As the sex phases were completely separate between individuals, the pattern of floral phenology may ensure that outcrossing strongly predominates. © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society, 2006, 152, 145,151. [source] THE EVOLUTION OF DIOECY, HETERODICHOGAMY, AND LABILE SEX EXPRESSION IN ACEREVOLUTION, Issue 11 2007S. S. Renner The northern hemisphere tree genus Acer comprises 124 species, most of them monoecious, but 13 dioecious. The monoecious species flower dichogamously, duodichogamously (male, female, male), or in some species heterodichogamously (two morphs that each produce male and female flowers but at reciprocal times). Dioecious species cannot engage in these temporal strategies. Using a phylogeny for 66 species and subspecies obtained from 6600 nucleotides of chloroplast introns, spacers, and a protein-coding gene, we address the hypothesis (Pannell and Verdú, Evolution 60: 660,673. 2006) that dioecy evolved from heterodichogamy. This hypothesis was based on phylogenetic analyses (Gleiser and Verdú, New Phytol. 165: 633,640. 2005) that included 29,39 species of Acer coded for five sexual strategies (duodichogamous monoecy, heterodichogamous androdioecy, heterodichogamous trioecy, dichogamous subdioecy, and dioecy) treated as ordered states or as a single continuous variable. When reviewing the basis for these scorings, we found errors that together with the small taxon sample, cast doubt on the earlier inferences. Based on published studies, we coded 56 species of Acer for four sexual strategies, dioecy, monoecy with dichogamous or duodichogamous flowering, monoecy with heterodichogamous flowering, or labile sex expression, in which individuals reverse their sex allocation depending on environment,phenotype interactions. Using Bayesian character mapping, we infer an average of 15 transformations, a third of them involving changes from monoecy-cum-duodichogamy to dioecy; less frequent were changes from this strategy to heterodichogamy; dioecy rarely reverts to other sexual systems. Contra the earlier inferences, we found no switches between heterodichogamy and dioecy. Unexpectedly, most of the species with labile sex expression are grouped together, suggesting that phenotypic plasticity in Acer may be a heritable sexual strategy. Because of the complex flowering phenologies, however, a concern remains that monoecy in Acer might not always be distinguishable from labile sex expression, which needs to be addressed by long-term monitoring of monoecious trees. The 13 dioecious species occur in phylogenetically disparate clades that date back to the Late Eocene and Oligocene, judging from a fossil-calibrated relaxed molecular clock. [source] LIFE-HISTORY DIFFERENTIATION AND THE MAINTENANCE OF MONOECY AND DIOECY IN SAGITTARIA LATIFOLIA (ALISMATACEAE)EVOLUTION, Issue 9 2003Marcel E. Dorken Abstract The existence of monoecious and dioecious populations within plant species is rare. This limits opportunities to investigate the ecological mechanisms responsible for the evolution and maintenance of these contrasting sexual systems. In Sagittaria latifolia, an aquatic flowering plant, monoecious and dioecious populations exist in close geographic proximity but occupy distinct wetland habitats differing in the relative importance of disturbance and competition, respectively. Life-history theory predicts contrasting evolutionary responses to these environmental conditions. We propose that the maintenance of monoecy and dioecy in S. latifolia is governed by ecological selection of divergent life-history strategies in contrasting habitats. Here we evaluate this hypothesis by comparing components of growth and reproduction between monoecious and dioecious populations under four conditions: natural populations, a uniform glasshouse environment, a common garden in which monoecious and dioecious populations and their F1 progeny were compared, and a transplant experiment using shaded and unshaded plots in a freshwater marsh. Plants from dioecious populations were larger in size and produced heavier corms in comparison with monoecious populations. Monoecious populations flowered earlier and produced more flowers, clonal ramets, and corms than dioecious populations. The life-history differences between the sexual systems were shown to have a quantitative genetic basis, with F1 progeny generally exhibiting intermediate trait values. Survival was highest for each sexual system in field plots that most closely resembled the habitats in which monoecious (unshaded) and dioecious (shaded) populations grow. These results demonstrate that monoecious and dioecious populations exhibit contrasting patterns of investment in traits involved with growth and reproduction. Selection for divergent life histories between monoecious and dioecious populations of S. latifolia appears to be the principal mechanism maintaining the integrity of the two sexual systems in areas of geographic overlap. [source] Consumptive emasculation: the ecological and evolutionary consequences of pollen theftBIOLOGICAL REVIEWS, Issue 2 2009Anna L. Hargreaves ABSTRACT Many of the diverse animals that consume floral rewards act as efficient pollinators; however, others ,steal' rewards without ,paying' for them by pollinating. In contrast to the extensive studies of the ecological and evolutionary consequences of nectar theft, pollen theft and its implications remain largely neglected, even though it affects plant reproduction more directly. Here we review existing studies of pollen theft and find that: (1) most pollen thieves pollinate other plant species, suggesting that theft generally arises from a mismatch between the flower and thief that precludes pollen deposition, (2) bees are the most commonly documented pollen thieves, and (3) the floral traits that typically facilitate pollen theft involve either spatial or temporal separation of sex function within flowers (herkogamy and dichogamy, respectively). Given that herkogamy and dichogamy occur commonly and that bees are globally the most important floral visitors, pollen theft is likely a greatly under-appreciated component of floral ecology and influence on floral evolution. We identify the mechanisms by which pollen theft can affect plant fitness, and review the evidence for theft-induced ecological effects, including pollen limitation. We then explore the consequences of pollen theft for the evolution of floral traits and sexual systems, and conclude by identifying key directions for future research. [source] | ||||||||||