Home About us Contact
|
Home About us Contact | ||
|
|
||
Flowering Period (flowering + period)
Selected AbstractsNectar ,theft' by hummingbird flower mites and its consequences for seed set in Moussonia deppeanaFUNCTIONAL ECOLOGY, Issue 1 2001Lara C. Summary 1,Mites (Acari: Mesostigmata: Ascidae) that live and feed in the flowers of about 100 plant species are transported in the nares of hummingbirds (Trochilidae). Mites may compete with hummingbirds for nectar secreted by the host plants, and this could affect the dynamics and reproductive outcomes of the mutualism between plants and their pollinating hummingbirds. 2,Here we combined field observations and experimental manipulations to assess the role of hummingbird flower mites (Tropicoseius sp. nov.) on nectar secretion and reproductive output of protandrous Moussonia deppeana (Schlecht. & Cham.) Hanst. (Gesneriaceae) during their flowering period in a cloud forest remnant. 3,During the 4 days that the flowers of M. deppeana last, flowers were visited exclusively by hummingbirds (Lampornis amethystinus). Bud production per inflorescence peaked in December. There were few open flowers per inflorescence in November, but numbers increased as the flowering season progressed (December and January). 4,The availability of each flower phase differed over the flowering season. Staminate-phase flowers were more abundant over the flowering season than pistillate-phase flowers. These differences were statistically significant over time. 5,Nectar availability was reduced by up to 50% in the presence of hummingbird flower mites. Over the 4 days of observation, significantly more nectar was secreted to flowers from which mites were excluded than to flowers with no mite exclusion. The same effect was observed during flowering, but mites consumed a greater percentage of the total nectar secreted in December. 6,Significantly more nectar was secreted during the staminate phase than in the pistillate phase, independent of time and treatment. 7,A manual pollination experiment suggested that mites act like secondary pollinators in this self-compatible, non-autogamous plant, at least in flowers that were not pollinated manually and had no access to pollinating hummingbirds. 8,Although seed production was not reduced significantly by flower mites, our results suggest that the presence of floral mites can affect pollen transmission, as the amount of nectar available to hummingbirds was reduced drastically. This can directly affect hummingbird foraging patterns and reduce the fitness of the host plants. [source] Allergenic pollen and pollen allergy in EuropeALLERGY, Issue 9 2007G. D'Amato The allergenic content of the atmosphere varies according to climate, geography and vegetation. Data on the presence and prevalence of allergenic airborne pollens, obtained from both aerobiological studies and allergological investigations, make it possible to design pollen calendars with the approximate flowering period of the plants in the sampling area. In this way, even though pollen production and dispersal from year to year depend on the patterns of preseason weather and on the conditions prevailing at the time of anthesis, it is usually possible to forecast the chances of encountering high atmospheric allergenic pollen concentrations in different areas. Aerobiological and allergological studies show that the pollen map of Europe is changing also as a result of cultural factors (for example, importation of plants such as birch and cypress for urban parklands), greater international travel (e.g. colonization by ragweed in France, northern Italy, Austria, Hungary etc.) and climate change. In this regard, the higher frequency of weather extremes, like thunderstorms, and increasing episodes of long range transport of allergenic pollen represent new challenges for researchers. Furthermore, in the last few years, experimental data on pollen and subpollen-particles structure, the pathogenetic role of pollen and the interaction between pollen and air pollutants, gave new insights into the mechanisms of respiratory allergic diseases. [source] Reproductive Biology of the Epiphytic Bromeliad Werauhia gladioliflora in a Premontane Tropical ForestPLANT BIOLOGY, Issue 2 2005A. Cascante-Marín Abstract: The floral phenology, fruit and seed production, and self-compatibility of Werauhia gladioliflora, an epiphytic bromeliad with a wide distribution, were studied in a premontane forest in the Monteverde area in Costa Rica. The species presents the pollination syndrome of chiropterophily, and it is visited by the small bats Hylonycteris underwoodi and Glossophaga commissarisi (Glossophaginae). The population flowering period extended from October to early December (end of rainy season) and seed dispersal occurred from February to April (dry season). Most plants opened a single flower per night, either every day or at one-day intervals during the flowering period. In natural conditions, the average fruit set amounted to almost half of the potential output, but individual fecundity (number of seeds) remained high. Seed number per fruit and germination capacity after artificial selfing and out-crossing treatments did not differ from natural pollination conditions. Werauhia gladioliflora exhibited high levels of autonomous self-pollination and self-compatibility at the individual and population level, characters associated with the epiphytic habitat. These reproductive traits are also associated with early colonizer species, yet life history traits, such as seed dispersal, seedling establishment success, and growth, are likely to have a major role in determining the presence of this species in the successional vegetation patches scattered over the studied premontane area. [source] Pollinators and Reproductive Success of the Wild Cucurbit Cucurbita maxima ssp. andreana (Cucurbitaceae)PLANT BIOLOGY, Issue 4 2001L. Ashworth Abstract: We studied the reproductive success and pollinators of Cucurbita maxima ssp. andreana in different disturbed habitats where it grows naturally. Data were obtained from three populations. One grew within a soybean crop, the other within a corn crop, and the third in an abandoned crop field. Cucurbita maxima ssp. andreana is an annual vine with a flowering period from December to April. Male flowers appear first, thereafter female and male flowers appear together. Flower lifetime (9 h) was similar in male and female flowers. The pollinator guild was comparable for the three populations but some differences in the frequency of the insect species were observed. Native bees were the main pollinators in the population in the abandoned field, while beetles pollinated the populations in crop fields. These differences were not linked with the pre-emergent reproductive success, fruit and seed set, or fruit quality. This is a self-compatible plant. Fruit and seed set and fruit traits (total mass, width and length of fruits, number of seeds per fruit, and seed mass) did not show significant differences between hand-cross and hand-self pollinated flowers. This wild cucurbit is a generalist with respect to pollinator guild, and flower visitors seem to be highly efficient in pollen transference. Cucurbita maxima ssp. andreana is well adapted to disturbed habitats because plants ripened fruits successfully, regardless of the group of insects visiting flowers. [source] Stability of the cleistogamous trait during the flowering period of oilseed rapePLANT BREEDING, Issue 1 2010M. Leflon With 2 figures and 4 tables Abstract At the field scale, the co-existence of different farming production systems requires strategies to prevent gene flow between adjacent crops. Oilseed rape produces pollen dispersed by wind and insects and the risks of pollen mediated gene flow are significant for this crop. Cleistogamy, the trait of non-opening flowers, could be used to reduce pollen flow. Cleistogamous oilseed rape genotypes were obtained by INRA in France and were bred in order to improve the stability of this trait. In this paper, we examine the reliability of the cleistogamous trait for two inbred lines. The flower opening level was measured at different dates during the flowering period in six field experiments (three sites × 2 years). The results showed that some flowers were partially opened with rates varying from 0.5% to 33% principally depending on genotypes, trials (site and year) and recording dates. Given that other studies have shown that cleistogamy could reduce pollen dispersal, we consider that, even when partially unstable, cleistogamy could be beneficially used in combination with other means in a containment strategy. [source] Resource distribution and the trade-off between seed number and seed weight: a comparison across crop speciesANNALS OF APPLIED BIOLOGY, Issue 1 2010B.L. Gambín In grain crops, total sink capacity is usually analysed in terms of two components, seed number and individual seed weight. Seed number and potential individual seed weight are established at a similar timing, around the flowering period, and seed weight at maturity is highly correlated with the potential established earlier. It is known that, within a species, available resources during the seed set period are distributed between both yield components, resulting in a trade-off between seed number and seed weight. Here we tested if this concept could apply for interspecific comparisons, where combinations of numbers and size across species could be related to the total available resources being either allocated to more seed or larger potential individual seed weight during the seed set period. Based on this, species differences in seed weight should be related to resource availability per seed around the period when seed number is determined. Resource availability per seed was estimated as the rate of increase in aboveground biomass per seed around the period of seed set. Data from 15 crop species differing in plant growth, seed number, seed weight and seed composition were analysed from available literature. Because species differed in seed composition, seed weight was analysed following an energy requirement approach. There was an interspecific trade-off relationship between seed number per unit of land area and seed weight (r = 0.92; F(1, 13) = 32.9; n = 15; P < 0.001). Seed weight of different species was positively correlated (r = 0.90; F(1, 13) = 52.9; n = 15; P < 0.001) with resource availability per seed around the seed set period. This correlation included contrasting species like quinoa (Chenopodium quinoa; ,100000 seeds m,2, ,4 mg equivalent-glucose seed,1) or peanut (Arachis hypogaea; ,800 seeds m,2, ,1000 mg equivalent-glucose seed,1). Seed number and individual seed weight combinations across species were related and could be explained considering resource availability when plants are adjusting their seed number to the growth environment and seeds are establishing their storage capacity. Available resources around the seed set period are proportionally allocated to produce either many small seeds or few larger seeds depending on the particular species. [source] Transgenic weed beets: possible, probable, avoidable?JOURNAL OF APPLIED ECOLOGY, Issue 4 2002Benoît Desplanque Summary 1Weed beets pose a serious problem for sugar beet Beta vulgaris crops. Traditionally, the only efficient method of weed control has been manual removal, but the introduction of transgenic herbicide-tolerant sugar beets may provide an alternative solution because non-tolerant weed beets can be destroyed by herbicide. We evaluated the possibility that new, transgenic, weed beets may arise by gene flow between wild and crop plants. 2In a study area in northern France, weed beets were present in variable densities in sugar beet fields of up to 80 weed beet plants m,2. Weed beets arise from a long-lived seed bank, with seeds germinating from depths of 5 cm or less. In addition, diploid F1 crop,wild hybrids and triploid variety bolters (individuals with a low vernalization requirement) were present in low densities in virtually all sugar beet fields. We found gene flow to be possible between all forms, illustrated by both overlapping flowering periods in the field and successful controlled cross-pollinations. 3The F1 crop,wild hybrids result from pollination in the seed-production region by wild plants possessing the dominant bolting allele B for flowering without experiencing a period of cold. In the case of a transgene for herbicide tolerance incorporated into male-sterile seed-bearer plants, such hybrids will contain both the herbicide-tolerance and the bolting allele. Contamination of the fields by transgenic weed beets will be the result unless bolters are removed manually. The same will apply in the case of a cytoplasmically inherited transgene. 4Incorporation of the transgene into the pollinator plants will prevent the immediate formation of transgenic weed beets. However, in sugar beet fields, variety bolters may successfully cross-pollinate with weed beets in neighbouring fields. The use of diploid pollinator plants instead of tetraploids will considerably enhance gene flow towards wild beets, and is not, therefore, an attractive option. 5In conclusion, the appearance of transgenic weed beets is possible but can best be retarded if the transgene for herbicide tolerance is incorporated into the tetraploid pollinator breeding line. [source] Importance of Silene latifolia ssp. alba and S. dioica (Caryophyllaceae) as host plants of the parasitic pollinator Hadena bicruris (Lepidoptera, Noctuidae)OIKOS, Issue 2 2004Sigrun Bopp With regards to pollination there exist several mutualistic relationships between Hadena -species and Caryophyllaceae. As mutualists have both negative and positive effects on their partners, mutualism is often betoken as reciprocative exploitation which may shift to parasitism if the exploitation of one partner becomes prevalent. Several Silene - and Saponaria -species are considered to be larval host plants of Hadena bicruris. Although Silene latifolia ssp. alba and S. dioica are frequently cited as hosts of the seed eating larvae, field and laboratory observations at Ulm were suggestive for only S. latifolia ssp. alba being a suitable host. Records of the oviposition behavior of H. bicruris made it evident that in fact a considerable number of eggs could be found in planted stands of both species. On the other hand, phenological data of the flowering periods and of the oviposition behavior of H. bicruris showed that S. latifolia ssp. alba is clearly preferred for oviposition if host selection is possible due to contemporaneous flowering of individuals of both plant species growing at close range. In addition, the flowering periods of S. latifolia ssp. alba and the periods of moth activity overlap to a large extent. This is not the case in S. dioica. Feeding experiences first indicated that the caterpillars may not prefer one of the species to the other, but comparison of the pupal weight of the animals reared on fruits of exclusively one of the species showed that the seeds of S. latifolia ssp. alba were more profitable for nutrition than those of S. dioica; the pupal weight of animals reared on seeds of the former species significantly exceeded that of animals reared on seeds of the latter one. The question arises if the symbiosis of H. bicruris and its hosts constitutes a stable situation or if an evolutionary shift to mutualism or parasitism will take place. [source] Reproduction of an early-flowering Mediterranean mountain narrow endemic (Armeria caespitosa) in a contracting mountain islandPLANT BIOLOGY, Issue 4 2009R. García-Camacho Abstract Reproduction at population lower edges is important for plant species persistence, especially in populations on contracting high-mountain islands. In this context, the ability of plants to reproduce in different microhabitats seems to be important to guarantee seed production in stressful environments, such as Mediterranean high mountains. We hypothesised that the warmer and drier conditions at the lower edge would be deleterious for the reproduction of Armeria caespitosa, an early-flowering plant. In addition, reproductive plasticity along this mountain gradient may also be microhabitat-dependent. We studied factors affecting the reproductive success of A. caespitosa, an endemic of the Spanish Sistema Central. We considered a complex set of predictors, including phenology, plant size and environmental factors at different scales using generalised estimating equations and generalised linear models. Microhabitat, together with the position in the altitudinal gradient and inter-annual variability affected the reproduction of A. caespitosa. In addition, individuals with longer flowering periods (duration of flowering) had significantly lower fruit set and a higher number of unviable seeds; delayed flowering peaks favoured the production of both viable and unviable fruits. Microhabitat variability over an altitudinal range is relevant for the reproduction of A. caespitosa, and is more important at the lower edge of the altitudinal range, where the species faces the most adverse conditions. In addition, the ability to reproduce in different microhabitats might increase the chances of the species to cope with environmental uncertainties under on-going climate warming. Finally, reproduction of this early-flowering plant is constrained by summer drought, which might shape its reproductive phenology. [source] Pollinators, flowering phenology and floral longevity in two Mediterranean Aristolochia species, with a review of flower visitor records for the genusPLANT BIOLOGY, Issue 1 2009R. Berjano Abstract The pollination of Aristolochia involves the temporary confinement of visitors inside the flower. A literature review has shown that some species are visited by one or a few dipteran families, while others are visited by a wider variety of dipterans, but only some of these are effective pollinators. We observed flowering phenology and temporal patterns of pollinator attendance in diverse populations of Aristolochia baetica and A. paucinervis, two species that grow in SW Spain, frequently in mixed populations. The two species had overlapping floral phenologies, extended flowering periods and long-lived flowers. A. baetica attracted a higher number of visitors than A. paucinervis. Drosophilids and, to a lesser extent, phorids, were the main pollinators of A. baetica, whereas in A. paucinervis, phorids were the only pollinators. Attendance to A. paucinervis flowers by phorids in mixed populations was markedly lower than in pure populations. This effect was more evident in years with lower pollinator density. Our results suggest that A. baetica and A. paucinervis may compete for pollinators in mixed populations. [source] Survival of Flower-visiting Chrysomelids during Non General-flowering Periods in Bornean Dipterocarp ForestsBIOTROPICA, Issue 5 2008Keiko Kishimoto-Yamada ABSTRACT In SE Asian rain forests, general flowering, a community-wide synchronous flowering, occurs at irregular and supra-annual intervals. During general flowering periods (GFP), most Dipterocarpaceae and many other trees flower profusely, while flowering plants are scant between GFP. During flowerless periods, anthophilous animals that depend on floral resources for food may suffer food shortages and subsequently decrease in abundance. Flower-visiting chrysomelid adults are major pollinators for some canopy tree species that flower during GFP. Although such chrysomelids feed on flower petals, the means by which they survive flowerless periods remains unknown. We determined the abundance of flower-visiting chrysomelids in GFP and non-GFP through light trap samples and examined the effects of the presence of young leaves and flowers of dipterocarps on local abundance, and feeding preferences of flower-visiting chrysomelids. We found no clear tendency that the chrysomelid species number and the abundance during GFP were consistently higher than those during non-GFP. Chrysomelid adults were more abundant on trees with many young leaves or flowers than on trees lacking young leaves and flowers. At least a few flower-visiting chrysomelids were observed feeding on young dipterocarp leaves and visiting young leaves and flowers of non-dipterocarps in the canopy during non-GFP. All results consistently suggest that chrysomelids are able to survive flowerless periods by feeding on the young leaves of dipterocarps and on the young leaves and flowers of non-dipterocarps; through this alternate feeding, chrysomelid populations are maintained at sufficient levels to function as effective pollinators of trees that flower during GFP. [source] | ||||||||||||||||||||||