TL;DR: In this article, the authors used hand pollination to investigate the effects of pollen from an invasive species (Lythrum salicaria) on seed set in a sympatric and co-flowering native congener (L. alatum).
Abstract: Competition for pollination can be an important factor in plant reproduction, but little attention has been given to the effect of the growing number of invasive plant species on pollination of native species. As a first step in understanding this threat, we used hand pollination to investigate the effects of pollen from an invasive species (Lythrum salicaria) on seed set in a sympatric and co-flowering native congener (L. alatum). Dispersal of fluorescent dyes in the field confirms that pollinators (bumble bees and honey bees) transfer pollen between species. To determine the potential effect of such interspecific pollen transfer on seed set of the native, we pollinated 773 flowers on 20 plants with one of three treatments: legitimate conspecific pollen, a mixture of conspecific and foreign pollen, and foreign pollen. The mixed-pollen treatment resulted in 28.8% lower seed set relative to conspecific pollination. Foreign crosses resulted in extremely low seed set. Observations of pollen germination indicate that events at the stigmatic surface contribute to the reduction in seed set for mixed pollination. Our results indicate that the impacts of invasive species may extend beyond vegetative competition to include competition for pollination.
TL;DR: Results from the other types of Bt corn suggest that pollen from the Cry1Ab and Cry1F, and experimental Cry9C hybrids, will have no acute effects on monarch butterfly larvae in field settings, and pollen contaminants, an artifact of pollen processing, can dramatically influence larval survival and weight gains and produce spurious results.
Abstract: Laboratory tests were conducted to establish the relative toxicity of Bacillus thuringiensis (Bt) toxins and pollen from Bt corn to monarch larvae. Toxins tested included Cry1Ab, Cry1Ac, Cry9C, and Cry1F. Three methods were used: (i) purified toxins incorporated into artificial diet, (ii) pollen collected from Bt corn hybrids applied directly to milkweed leaf discs, and (iii) Bt pollen contaminated with corn tassel material applied directly to milkweed leaf discs. Bioassays of purified Bt toxins indicate that Cry9C and Cry1F proteins are relatively nontoxic to monarch first instars, whereas first instars are sensitive to Cry1Ab and Cry1Ac proteins. Older instars were 12 to 23 times less susceptible to Cry1Ab toxin compared with first instars. Pollen bioassays suggest that pollen contaminants, an artifact of pollen processing, can dramatically influence larval survival and weight gains and produce spurious results. The only transgenic corn pollen that consistently affected monarch larvae was from Cry1Ab event 176 hybrids, currently <2% corn planted and for which re-registration has not been applied. Results from the other types of Bt corn suggest that pollen from the Cry1Ab (events Bt11 and Mon810) and Cry1F, and experimental Cry9C hybrids, will have no acute effects on monarch butterfly larvae in field settings.
TL;DR: The heat-sensitive genotype experienced reduced pollen viability and reduced yield in high-temperature experiments conducted in both the greenhouse and field and under heat stress showed anther and pollen characteristics that were generally similar to the low temperature controls.
Abstract: High ambient temperature (32/27 °C, day/night, 12 h photoperiod) applied prior to anthesis to Phaseolus vulgaris plants results in abnormal pollen and anther development during microsporogenesis. Scanning and transmission electron microscopy were used to examine anther and pollen morphology and pollen wall architecture after heat stress was applied to two genotypes that differ with respect to yield potential under high-temperature field conditions: one, a heat-sensitive, Mesoamerican genotype, A55, the second, a heat-tolerant, Andean genotype, G122. High-temperature treatment of both genotypes was applied 1-13 d before anthesis. Under heat stress, the heat-tolerant genotype showed anther and pollen characteristics that were generally similar to the low temperature controls. In contrast, after 9 d of heat treatment before anthesis, the anthers of the heat-sensitive genotype were indehiscent and contained abnormal pollen. Pollen wall architecture was also affected in the 12 and 13 d treatments. In addition to the morphological changes, the heat-sensitive genotype also experienced reduced pollen viability and reduced yield in high-temperature experiments conducted in both the greenhouse and field.
TL;DR: In a greenhouse metabolism study, sunflowers were seed-treated with radiolabelled imidacloprid in a 700 g kg-1 WS formulation (Gaucho WS 70), and the nature of the resulting residues in nectar and pollen was determined.
Abstract: In a greenhouse metabolism study, sunflowers were seed-treated with radiolabelled imidacloprid in a 700 g kg-1 WS formulation (Gaucho WS 70) at 0.7 mg AI per seed, and the nature of the resulting residues in nectar and pollen was determined. Only the parent compound and no metabolites were detected in nectar and pollen of these seed-treated sunflower plants (limit of detection < 0.001 mg kg-1). In standard LD50 laboratory tests, imidacloprid showed high oral toxicity to honeybees (Apis mellifera), with LD50 values between 3.7 and 40.9 ng per bee, corresponding to a lethal food concentration between 0.14 and 1.57 mg kg-1. The residue level of imidacloprid in nectar and pollen of seed-treated sunflower plants in the field was negligible. Under field-growing conditions no residues were detected (limit of detection: 0.0015 mg kg-1) in either nectar or pollen. There were also no detectable residues in nectar and pollen of sunflowers planted as a succeeding crop in soils which previously had been cropped with imidacloprid seed-treated plants. Chronic feeding experiments with sunflower honey fortified with 0.002, 0.005, 0.010 and 0.020 mg kg-1 imidacloprid were conducted to assess potential long-term adverse effects on honeybee colonies. Testing end-points in this 39-day feeding study were mortality, feeding activity, wax/comb production, breeding performance and colony vitality. Even at the highest test concentration, imidacloprid showed no adverse effects on the development of the exposed bee colonies. This no-adverse-effect concentration of 0.020 mg kg-1 compares with a field residue level of less than 0.0015 mg kg-1 (= limit of detection in the field residue studies) which clearly shows that a sunflower seed dressing with imidacloprid poses no risk to honeybees. This conclusion is confirmed by observations made in more than 10 field studies and several tunnel tests.
TL;DR: In this article, the content of polyphenol compounds was found to be correlated with the antioxidant and radical scavenging activity of the extracts of bee-collected flower pollen, which can be regarded as effective natural and functional dietary food supplement.
Abstract: Bee-collected pollen is an apicultural product which is composed of nutritionally valuable substances and contains considerable amounts polyphenol substances (8.2 mg/g) which may act as potent antioxidants. By preparing ethanol, methanol/water and water extracts of natural pollen the content of polyphenol compounds could be significantly increased (21.4–24.6 mg/g). Correspondingly, bee-collected pollen extracts show considerable antiradical activity (PI: 35% inhibition) which is significantly increased in the pollen extracts (PI: 39–53% inhibition). The highest degree of radical scavenging activity is found in the ethanol extract, which also has the highest concentration of polyphenol substances. For this reason, it can be assumed that there is a general correlation between the content of total polyphenols and the antioxidant and radical scavenging activity of the pollen preparations. Thus, the prepared extracts of bee-collected flower pollen may be regarded as effective natural and functional dietary food supplement due to their remarkable content of polyphenol substances and significant radical scavenging capacity with special regard to their nutritional–physiological implications and their health promoting effect.
TL;DR: Pollen longevity was tested by collecting pollen at dehiscence and it was found that the introduction of improved varieties into exposing it in a thin layer in the open air and sunshine for prescribed these regions will result in the loss of genetic diversity.
Abstract: to 10 000 yr has resulted in many distinct landraces of maize in south-central and southwestern Mexico (GoodPollen is an important vector of gene flow in maize (Zea mays man, 1988). L.). Experiments were conducted to investigate the duration of pollen Those who conserve maize genetic resources are conviability and the effectiveness of isolation distance for controlling gene flow. Pollen longevity was tested by collecting pollen at dehiscence and cerned that the introduction of improved varieties into exposing it in a thin layer in the open air and sunshine for prescribed these regions will result in the loss of genetic diversity. time periods before assessing pollen viability by measuring seed set Iltis (1974) proposed the creation of in situ conservation after pollination and scoring visual appearance. Isolation distance of germplasm to complement ex situ conservation stratefficacy was evaluated by growing 12.8-m
TL;DR: Measures of pollen-transfer effectiveness do not provide a complete assessment of pollination value, but can serve as a general, inexpensive tool for pre-screening possible alternative pollinators.
Abstract: Summary
1
To help evaluate the worth of alternative pollinators in agriculture, we present a theoretical framework for comparing the effectiveness of two or more pollinators by measuring pollen removal and deposition.
2
We report pollen removal and deposition data by Apis mellifera and Bombus spp. during single visits to four cultivars of apples (Golden Delicious, Starkrimson Delicious, Empire/MacIntosh and Rome) and Mission almond.
3
Apis and Bombus removed similar amounts of pollen from apple flowers but Bombus deposited more pollen on stigmas. Pollen-collecting bees removed more pollen from apple anthers than nectar-collecting bees. Apis that approached nectaries laterally deposited substantially less pollen than other visitors.
4
Apis and Bombus removed and deposited similar amounts of pollen on almond flowers. Apis tended to remove more during pollen-collecting visits than nectar-collecting visits. The type of resource sought did not significantly influence deposition.
5
Based on removal and deposition data, additions of Bombus may increase pollen delivery in apple orchards but reduce pollen delivery in almond orchards if Apis already serve as primary pollinators. Additional data on inter-tree and inter-row flights would be necessary to know how much these changes in pollen transfer might affect fertilization.
6
Measures of pollen-transfer effectiveness do not provide a complete assessment of pollination value, but can serve as a general, inexpensive tool for pre-screening possible alternative pollinators.
TL;DR: This study shows that the commonly assumed pathway from low pollinator availability to strong pollen limitation is not always correct but supports the view that selection on floral traits is positively related to the degree of pollen limitation, and examines how abiotic environmental conditions affect pollen limitation on female reproductive success and pollinator flower visitation.
Abstract: Phenotypic selection on flower size in animal-pollinated plants can only occur when fitness is limited by pollinator visitation and when there is a relationship between flower size and pollinator attraction. The purpose of this study was (a) to examine how abiotic environmental conditions affect pollen limitation on female reproductive success and pollinator flower visitation and (b) to reveal whether phenotypic selection on floral traits in an alpine flowering species varied across an abiotic environmental gradient. In alpine populations of the perennial herb Ranunculus acris, I found that female reproductive success in a low-altitude population was significantly increased by experimental pollen addition, while plants at a higher altitude population did not respond to this treatment, presumably because low temperatures limited their seed production. At the low altitude, pollinators (muscoid flies) preferred to visit relatively large flowers, while no sign of flower discrimination occurred at the high altitude. Phenotypic selection regression analysis found that selection on flower size traits was more intense and frequent at the low-altitude compared to the high-altitude population. This result is consistent with the findings of stronger pollen limitation on seed set and the existence of pollinator discrimination on flower size at the low altitude compared to the high altitude. Pollinator visitation rates to flowers were nearly three times higher at the low altitude, compared to the high altitude. Thus, this study shows that the commonly assumed pathway from low pollinator availability to strong pollen limitation is not always correct but supports the view that selection on floral traits is positively related to the degree of pollen limitation. In R. acris environmental factors interact with pollen availability in determining the reproductive success of plants, and this interrupts the pathway from low pollinator availability via significant pollen limitation to selection on floral traits.
TL;DR: Analysis of the syntenic region in Brassica oleracea revealed even greater divergence, but a similar clustering of the genes, which suggests allelic flexibility may promote speciation in plants.
Abstract: The pollen extracellular matrix contains proteins mediating species specificity and components needed for efficient pollination. We identified all proteins >10 kilodaltons in the Arabidopsis pollen coating and showed that most of the corresponding genes reside in two genomic clusters. One cluster encodes six lipases, whereas the other contains six lipid-binding oleosin genes, including GRP17, a gene that promotes efficient pollination. Individual oleosins exhibit extensive divergence between ecotypes, but the entire cluster remains intact. Analysis of the syntenic region in Brassica oleracea revealed even greater divergence, but a similar clustering of the genes. Such allelic flexibility may promote speciation in plants.
TL;DR: In this paper, the ice nucleating ability of four kinds of pollen in the deposition and the condensation freezing modes was investigated, and the results showed that all investigated pollen were able to take up significant amounts of water from a humid environment into their interior by capillary effect.
TL;DR: The function of a conserved GTGA motif shared between the tobacco g10 and tomato lat56 promoters was demonstrated in g10, providing further functional evidence for the conservation of mechanisms for the regulation of late pollen genes across species.
Abstract: The tobacco gene g10 is preferentially and maximally expressed in mature pollen, shows homology to pectate lyases, and is the putative homologue of the tomato gene lat56. Analysis of regulatory elements within the g10 promoter was carried out to verify the importance of putative regulatory sequence motifs. Analysis of transgenic plants showed that 1190 bp of g10 5' sequence directed preferential expression of GUS in pollen, with bimodal peaks of expression just before and during pollen mitosis I, and in mature anthers. This was confirmed by northern analysis of native g10 transcripts in isolated spores. Transient expression analysis defined the minimal g10 promoter region capable of directing expression in pollen as -86 to +217. Three upstream regions within -427 bp modulate the expression from g10. Gain-of-function analyses showed that the region from -106 to -53 could enhance pollen-specific expression of a minimal CaMV 35S promoter. These analyses further showed that sequences upstream of -86 modulate expression in pollen, but are not essential for preferential pollen expression. The function of a conserved GTGA motif shared between the tobacco g10 and tomato lat56 promoters was demonstrated in g10. Thus, further functional evidence is provided for the conservation of mechanisms for the regulation of late pollen genes across species.
TL;DR: The focus of this study is to investigate the regulatory role of K(+) influx in Arabidopsis pollen germination and pollen tube growth using agar-containing media and to study the physiological importance of potassium influx mediated by the inward K(+)-channels during Arabdopsis pollen Germination and tube growth.
Abstract: The focus of this study is to investigate the regulatory role of K(+) influx in Arabidopsis pollen germination and pollen tube growth. Using agar-containing media, in vitro methods for Arabidopsis pollen germination have been successfully established for the first time. The pollen germination percentage was nearly 75% and the average pollen tube length reached 135 microm after a 6 h incubation. A decrease in external K(+) concentration from 1 mM to 35 microM resulted in 30% inhibition of pollen germination and 40% inhibition of pollen tube growth. An increase in external K(+) concentration from 1 mM to 30 mM stimulated pollen tube growth but inhibited pollen germination. To study how K(+) influx is associated with pollen germination and tube growth, regulation of the inward K(+) channels in the pollen plasma membrane was investigated by conducting patch-clamp whole-cell recording with pollen protoplasts. K(+) currents were first identified in Arabidopsis pollen protoplasts. The inward K(+) currents were insensitive to changes in cytoplasmic Ca(2+) but were inhibited by a high concentration of external Ca(2+). A decrease of external Ca(2+) concentration from 10 mM (control) to 1 mM had no significant effect on the inward K(+) currents, while an increase of external Ca(2+) concentration from 10 mM to 50 mM inhibited the inward K(+) currents by 46%. Changes in external pH significantly affected the magnitude, conductance, voltage-independent maximal conductance, and activation kinetics of the inward K(+) currents. The physiological importance of potassium influx mediated by the inward K(+)-channels during Arabidopsis pollen germination and tube growth is discussed.
TL;DR: The isolation and molecular characterization of DEX1 and morphological and ultrastructural analyses of dex1 plants reveal a novel plant protein that is predicted to be membrane associated and contains several potential calcium-binding domains.
Abstract: To identify factors that are required for proper pollen wall formation, we have characterized the T-DNA-tagged, dex1 mutation of Arabidopsis, which results in defective pollen wall pattern formation. This study reports the isolation and molecular characterization of DEX1 and morphological and ultrastructural analyses of dex1 plants. DEX1 encodes a novel plant protein that is predicted to be membrane associated and contains several potential calcium-binding domains. Pollen wall development in dex1 plants parallels that of wild-type plants until the early tetrad stage. In dex1 plants, primexine deposition is delayed and significantly reduced. The normal rippling of the plasma membrane and production of spacers observed in wild-type plants is also absent in the mutant. Sporopollenin is produced and randomly deposited on the plasma membrane in dex1 plants. However, it does not appear to be anchored to the microspore and forms large aggregates on the developing microspore and the locule walls. Based on the structure of DEX1 and the phenotype of dex1 plants, several potential roles for the protein are proposed.
TL;DR: The effects of Bt11 and Mon810 pollen on the survivorship of larvae feeding 14 to 22 days on milkweeds in fields were negligible and survivorship and weight gain were drastically reduced in non-Bt fields treated with λ-cyhalothrin.
Abstract: Survival and growth of monarch larvae, Danaus plexippus (L.), after exposure to either Cry1Ab-expressing pollen from three Bacillus thuringiensis (Bt) corn (Zea mays L.) events differing in toxin expression or to the insecticide, λ-cyhalothrin, were examined in field studies. First instars exposed to low doses (≈22 grains per cm2) of event-176 pollen gained 18% less weight than those exposed to Bt11 or Mon810 pollen after a 5-day exposure period. Larvae exposed to 67 pollen grains per cm2 on milkweed leaves from within an event-176 field exhibited 60% lower survivorship and 42% less weight gain compared with those exposed to leaves from outside the field. In contrast, Bt11 pollen had no effect on growth to adulthood or survival of first or third instars exposed for 5 days to ≈55 and 97 pollen grains per cm2, respectively. Similarly, no differences in larval survivorship were observed after a 4-day exposure period to leaves with 504–586 (within fields) or 18–22 (outside the field) pollen grains per cm2 collected from Bt11 and non-Bt sweet-corn fields. However, survivorship and weight gain were drastically reduced in non-Bt fields treated with λ-cyhalothrin. The effects of Bt11 and Mon810 pollen on the survivorship of larvae feeding 14 to 22 days on milkweeds in fields were negligible. Further studies should examine the lifetime and reproductive impact of Bt11 and Mon810 pollen on monarchs after long-term exposure to naturally deposited pollen.
TL;DR: Overall, the results indicate that honeybees respond to deficiencies in the quantity or quality of their pollen reserves by increasing the gross amount of pollen returned to the colony, rather than by specializing in collecting pollen with a greater protein content.
Abstract: Individual and colony-level foraging behaviors were evaluated in response to changes in the quantity or nutritional quality of pollen stored within honeybee (Apis mellifera L.) colonies. Colonies were housed in vertical, three-frame observation hives situated inside a building, with entrances leading to the exterior. Before receiving treatments, all colonies were deprived of pollen for 5 days and pollen foragers were marked. In one treatment group, colony pollen reserves were quantitatively manipulated to a low or high level, either by starving colonies of pollen or by providing them with a fully provisioned frame of pollen composed of mixed species. In another treatment group, pollen reserves were qualitatively manipulated by removing pollen stores from colonies and replacing them with low- or high-protein pollen supplements. After applying treatments, foraging rates were measured four times per day and pollen pellets were collected from experienced and inexperienced foragers to determine their weight, species composition, and protein content. Honeybee colonies responded to decreases in the quantity or quality of pollen reserves by increasing the proportion of pollen foragers in their foraging populations, without increasing the overall foraging rate. Manipulation of pollen stores had no effect on the breadth of floral species collected by colonies, or their preferences for the size or protein content of pollen grains. In addition, treatments had no effect on the weight of pollen loads collected by individual foragers or the number of floral species collected per foraging trip. However, significant changes in foraging behavior were detected in relation to the experience level of foragers. Irrespective of treatment group, inexperienced foragers exerted greater effort by collecting heavier pollen loads and also sampled their floral environment more extensively than experienced foragers. Overall, our results indicate that honeybees respond to deficiencies in the quantity or quality of their pollen reserves by increasing the gross amount of pollen returned to the colony, rather than by specializing in collecting pollen with a greater protein content. Individual pollen foragers appear to be insensitive to the quality of pollen they collect, indicating that colony-level feedback is necessary to regulate the flow of protein to and within the colony. Colonies may respond to changes in the quality of their pollen stores by adjusting the numbers of inexperienced to experienced foragers within their foraging populations.
TL;DR: The understanding of the mechanisms controlling the various aspects of pollen tube development has a direct relevance to biotechnological applications since it represents a starting point to modify crop production and it enhances the knowledge on molecular and cellular events controlling the tip growth mechanism.
Abstract: Pollen, the male gametophyte of higher plants, is a biological system playing a central role in sexual plant reproduction (Cresti et al., 1992). The understanding of the mechanisms controlling the various aspects of pollen tube development has a direct relevance to biotechnological applications since it represents a starting point to modify crop production and it enhances the knowledge on molecular and cellular events controlling the tip growth mechanism. When pollen arrives on the surface of a compatible stigma it undergoes a complex series of regulated cytoplasmic rearrangements leading to the emergence of a cylindrical structure known as pollen tube, with the main purpose to carry and deliver sperm cells to the embryo sac for the double fertilization. In vivo, pollen tubes grow through the transmitting tissue in the style and, since they never penetrate stigmatic cells, the mechanisms involving cell-cell recognition and signalling must exist to guide pollen tubes to the ovary. For this purpose, specific molecules of the transmitting tissue acting as adhesive substrate, attractants and stimulators of pollen tube elongation (Lord and Sanders, 1992) have been identified and characterized in several angiosperms but pollen tube targets of these external stimuli and the nature of these interactions have not been fully understood at the molecular level (Frankling-Tong, 1999).
TL;DR: In this article, three sediment cores from the Braganca Peninsula located in the coastal region in the north-eastern portion of Para State have been studied by pollen analysis to reconstruct Holocene environmental changes and dynamics of the mangrove ecosystem.
TL;DR: The results suggest that fragmentation and thinning of blue oak woodlands may reduce pollen availability and limit reproduction in this wind-pollinated species.
Abstract: Human activities are fragmenting forests and woodlands worldwide, but the impact of reduced tree population densities on pollen transfer in wind-pollinated trees is poorly understood. In a 4-year study, we evaluated relationships among stand density, pollen availability, and seed production in a thinned and fragmented population of blue oak (Quercus douglasii). Geographic coordinates were established and flowering interval determined for 100 contiguous trees. The number of neighboring trees within 60 m that released pollen during each tree's flowering period was calculated and relationships with acorn production explored using multiple regression. We evaluated the effects of female flower production, average temperature, and relative humidity during the pollination period, and number of pollen-producing neighbors on individual trees' acorn production. All factors except temperature were significant in at least one of the years of our study, but the combination of factors influencing acorn production varied among years. In 1996, a year of large acorn crop size, acorn production was significantly positively associated with number of neighboring pollen producers and density of female flowers. In 1997, 1998, and 1999, many trees produced few or no acorns, and significant associations between number of pollen-producing neighbors and acorn production were only apparent among moderately to highly reproductive trees. Acorn production by these reproductive trees in 1997 was significantly positively associated with number of neighboring pollen producers and significantly negatively associated with average relative humidity during the pollination period. In 1998, no analysis was possible, because too few trees produced a moderate to large acorn crop. Only density of female flowers was significantly associated with acorn production of moderately to highly reproductive trees in 1999. The effect of spatial scale was also investigated by conducting analyses with pollen producers counted in radii ranging from 30 m to 80 m. The association between number of pollen-producing neighbors and acorn production was strongest when neighborhood sizes of 60 m or larger were considered. Our results suggest that fragmentation and thinning of blue oak woodlands may reduce pollen availability and limit reproduction in this wind-pollinated species.
TL;DR: In this article, the Atacama Lake sediments and pollen, spores and algae from the high-elevation endorheic Laguna Miscanti (22°45′S, 67°45')W, 4140 m a.s.l., 13.5 km2 water surface, 10 m deep) in the Ataca Desert of northern Chile provide information about abrupt and high amplitude changes in effective moisture.
Abstract: Lake sediments and pollen, spores and algae from the high-elevation endorheic Laguna Miscanti (22°45′S, 67°45′W, 4140 m a.s.l., 13.5 km2 water surface, 10 m deep) in the Atacama Desert of northern Chile provide information about abrupt and high amplitude changes in effective moisture. Although the lack of terrestrial organic macrofossils and the presence of a significant 14C reservoir effect make radiocarbon dating of lake sediments very difficult, we propose the following palaeoenvironmental history. An initial shallow freshwater lake (ca. 22,000 14C years BP) disappeared during the extremely dry conditions of the Last Glacial Maximum (LGM; 18,000 14C years BP). That section is devoid of pollen. The late-glacial lake transgression started around 12,000 14C years BP, peaked in two phases between ca. 11,000 and <9000 14C years BP, and terminated around 8000 14C years BP. Effective moisture increased more than three times compared to modern conditions (∼200 mm precipitation), and a relatively dense terrestrial vegetation was established. Very shallow hypersaline lacustrine conditions prevailed during the mid-Holocene until ca. 3600 14C years BP. However, numerous drying and wetting cycles suggest frequent changes in moisture, maybe even individual storms during the mid-Holocene. After several humid spells, modern conditions were reached at ca. 3000 14C years BP. Comparison between limnogeological data and pollen of terrestrial plants suggest century-scale response lags. Relatively constant concentrations of long-distance transported pollen from lowlands east of the Andes suggest similar atmospheric circulation patterns (mainly tropical summer rainfall) throughout the entire period of time. These findings compare favorably with other regional paleoenvironmental data.
TL;DR: It is established that SP11/SCR is the sole male determinant of SI in the genus Brassica sp.
Abstract: Many flowering plants have evolved self-incompatibility (SI) systems to prevent inbreeding. In the Brassicaceae, SI is genetically controlled by a single polymorphic locus, termed the S-locus. Pollen rejection occurs when stigma and pollen share the same S-haplotype. Recognition of S-haplotype specificity has recently been shown to involve at least two S-locus genes, S-receptor kinase (SRK) and S-locus protein 11 or S-locus Cys-rich (SP11/SCR). SRK encodes a polymorphic membrane-spanning protein kinase, which is the sole female determinant of the S-haplotype specificity. SP11/SCR encodes a highly polymorphic Cys-rich small basic protein specifically expressed in the anther tapetum and in pollen. In cauliflower (B. oleracea), the gain-of-function approach has demonstrated that an allele of SP11/SCR encodes the male determinant of S-specificity. Here we examined the function of two alleles of SP11/SCR of B. rapa by the same approach and further established that SP11/SCR is the sole male determinant of SI in the genus Brassica sp. Our results also suggested that the 522-bp 5'-upstream region of the S9-SP11 gene used to drive the transgene contained all the regulatory elements required for the unique sporophytic/gametophytic expression observed for the native SP11 gene. Promoter deletion analyses suggested that the highly conserved 192-bp upstream region was sufficient for driving this unique expression. Furthermore, immunohistochemical analyses revealed that the protein product of the SP11 transgene was present in the tapetum and pollen, and that in pollen of late developmental stages, the SP11 protein was mainly localized in the pollen coat, a finding consistent with its expected biological role.
TL;DR: Floral buds were most sensitive to high temperature at 4 DBA and at anthesis, coinciding with micro-sporogenesis and pollination or fertilisation, respectively, and fruit-set was reduced by 6% °C -1 .
Abstract: Peanut ( Arachis hypogaea L.) crops are often exposed to day temperatures > 35°C for short periods during flowering, resulting in lower yields. Research was conducted to study and quantify the effects of short episodes (1-6 d) of high temperatures during the pre- and post-anthesis stages of floral development on fruit-set, pollen viability, germination and tube growth. Plants of peanut cv. ICGV-86015 were grown in controlled environments at 28/22°C (day/night). High daytime air temperature treatments ranging from 28 (control) to 48°C were imposed at different times between 6 d before anthesis (DBA) and 6 d after anthesis (DAA) for 1, 3 or 6 d. Floral buds or flowers were tagged at different stages to determine fruit-set. Exposure to bud (tissue) temperature ≥ 39°C for 1 d significantly reduced fruit-set compared to the control at 28°C, and the magnitude of the reduction varied with stage of floral development. Floral buds were most sensitive to high temperature at 4 DBA and at anthesis, coinciding with micro-sporogenesis and pollination or fertilisation, respectively. The critical bud temperature at these stages was 33°C, above which fruit-set was reduced by 6% °C -1 . Lower fruit-set due to high temperatures at pre-anthesis and anthesis stages were due to pollen sterility and retarded pollen tube growth, respectively.
TL;DR: The larvae's mean capping age significantly correlated with the mean pollen income: the less pollen was stored by the hive during the larvae's development, the earlier the larvae were capped, and this strategy compensates for a shortage of supply by reducing demand.
Abstract: We observed the impact of bad pollen supply (non-foraging due to artificial rain and pollen removal under poor-foraging conditions) on the survival of honey bee larvae, and on the total development time from egg-laying to the capping of a larval cell. Five days of non-foraging led to cannibalism of larvae younger than 3 days old and to a shortening of the time until larvae were sealed, but 4- and 5-day-old larvae survived even worse pollen supply situations. Manual pollen removal and reduction of income (pollen trap) induced cannibalism of younger larvae. The larvae's mean capping age significantly correlated with the mean pollen income: the less pollen was stored by the hive during the larvae's development, the earlier the larvae were capped. Both behavioral patterns lead to a quick reduction in the amount of unsealed older brood in response to a shortage of available protein. Older larvae have the highest pollen demand, so this strategy compensates for a shortage of supply by reducing demand. Additionally worker jelly gets enriched by protein gained from cannibalism, and the early capping of older larvae saves the oldest part of the brood, which represents the highest broodcare investment.
TL;DR: In this review genetic, cell biological and molecular aspects of in vitro microspore development are presented and put in the context of current basic and applied plant science.
Abstract: The microspore is at the centre of a variety of topics in modern plant science and breeding Isolated microspore cultures have the remarkable quality of resembling the alternation of generations in the life cycle of angiosperms, ie the change between the diploid sporophytec and the haploid gametophytec generation Although the natural destination of microspore development is to differentiate into mature pollen and accomplish fertilization, isolated and in vitro cultured microspores or young pollen grains can either differentiate into mature, fertile pollen (the male gametophytes) by culture in a rich medium without stress, or divide repeatedly and develop into embryos (sporophytes) after a stress treatment As experimental systems, microspore cultures are used to investigate pollen development and pollination, embryogenesis, totipotency, cytodifferentiation, cell cycle, phase change and the role of stress in development As a tool in genetic engineering, they can be used to produce doubled haploids (recombinant inbreds) for plant breeding and gene mapping, to overcome crossing barriers (male sterility and self-incompatibility), to induce and select for mutants and to create transgenic plants In this review genetic, cell biological and molecular aspects of in vitro microspore development are presented and put in the context of current basic and applied plant science
TL;DR: Evidence is provided for the possibility that polyphenolic compounds in pollen of plants are indicators of solar UV-B and may be applied as a new proxy for the reconstruction of historic variation in solarUV-B levels.
Abstract: UV-B absorbance and UV-B absorbing compounds (UACs) of the pollen of Vicia faba, Betula pendula , Helleborus foetidus and Pinus sylvestris were studied. Sequential extraction demonstrated considerable UV-B absorbance both in the soluble (acid methanol) and insoluble sporopollenin (acetolysis resistant residue) fractions of UACs, while the wall-bound fraction of UACs was small. The UV-B absorbance of the soluble and sporopollenin fraction of pollen of Vicia faba plants exposed to enhanced UV-B (10 kJ m −2 day −1 UV-B BE ) was higher than that of plants that received 0 kJ m −2 day −1 UV-B BE . Pyrolysis gas chromatography–mass spectrometry (py-GC–MS) analysis of pollen demonstrated that p -coumaric acid and ferulic acid formed part of the sporopollenin fraction of the pollen. The amount of these aromatic monomers in the sporopollenin of Vicia faba appeared to increase in response to enhanced UV-B (10 kJ m −2 day −1 UV-B BE ). The detection limit of pyGC–MS was sufficiently low to quantify these phenolic acids in ten pollen grains of Betula and Pinus .The experimental data presented provide evidence for the possibility that polyphenolic compounds in pollen of plants are indicators of solar UV-B and may be applied as a new proxy for the reconstruction of historic variation in solar UV-B levels.
TL;DR: Investigation of the occurrence of gene flow from transgenic rice to non-transgenic rice plants under agronomic conditions using a herbicide resistance gene as a tracer marker showed that pollination of recipient plants with pollen of the transgenic source occurred at a significant frequency.
Abstract: Development of plant genetic engineering has led to the deployment of transgenic crops and, simultaneously, to the need for a thorough assessment of the risks associated with their environmental release. This study investigated the occurrence of gene flow from transgenic rice to non-transgenic rice plants under agronomic conditions using a herbicide resistance gene as a tracer marker. Two field experiments were established in the paddy fields of two main Mediterranean rice-growing areas of Spain and Italy. In both locations analyses of phenotypic, molecular and segregation data showed that pollination of recipient plants with pollen of the transgenic source occurred at a significant frequency. A gene flow slightly lower than 0.1% was detected in a normal side-by-side plot design. Similar results were found in a circular plot when the plants were placed at 1-m distance from the transgenic central nucleus. A strong asymmetric distribution of the gene flow was detected among this circle and highest values (0.53%) were recorded following the direction of the dominant wind. A significant lowest value (0.01%) was found in the other circle (5 m from the transgenic plants) as was expected according to the characteristics of rice pollen. Such circular-field trial designs could also prove to be very useful in studying the gene flow to other commercial cultivars of rice with the aim of establishing strategies to prevent pollen dispersal from commercial transgenic fields to the neighbouring conventional fields.
TL;DR: A review of self-incompatibility systems in flowering plants highlights the recent advances made towards understanding the cellular mechanisms involved and discusses the striking differences between these systems.
Abstract: Self-incompatibility is a widespread mechanism in flowering plants that prevents inbreeding and promotes outcrossing. The self-incompatibility response is genetically controlled by one or more multi-allelic loci, and relies on a series of complex cellular interactions between the self-incompatible pollen and pistil. Although self-incompatibility functions ultimately to prevent self-fertilization, flowering plants have evolved several unique mechanisms for rejecting the self-incompatible pollen. The self-incompatibility system in the Solanaceae makes use of a multi-allelic RNase in the pistil to block incompatible pollen tube growth. In contrast, the Papaveraceae system appears to have complex cellular responses such as calcium fluxes, actin rearrangements, and programmed cell death occurring in the incompatible pollen tube. Finally, the Brassicaceae system has a receptor kinase signalling pathway activated in the pistil leading to pollen rejection. This review highlights the recent advances made towards understanding the cellular mechanisms involved in these self-incompatibility systems and discusses the striking differences between these systems.
TL;DR: The aim of this paper is to draw attention to partially hydrated pollen, namely, pollen grains having a high water content (>30%); this type of pollen is more frequent than previously thought.
Abstract: The aim of this paper is to draw attention to partially hydrated pollen, namely, pollen grains having a high water content (>30%); this type of pollen is more frequent than previously thought. Various cyto-physiological strategies are used to retain water during exposure and dispersal such as cytoplasm carbohydrates; in the absence of such strategies, fast pollination must be ensured, because uncontrolled loss of water leads to pollen death. On the other hand, a state of partial hydration allows a fast tube emission (even within 3–5 min). Several methods for determining the hydration status of pollen at anthesis are proposed.
TL;DR: The results of the multiple regression analysis show that the variables exerting the greatest influence on the pollen index were rainfall in March and temperatures over the months prior to the flowering period, while temperature proved the best variable for this prediction.
Abstract: Data on predicted average and maximum airborne pollen concentrations and the dates on which these maximum values are expected are of undoubted value to allergists and allergy sufferers, as well as to agronomists. This paper reports on the development of predictive models for calculating total annual pollen output, on the basis of pollen and weather data compiled over the last 19 years (1982–2000) for Cordoba (Spain). Models were tested in order to predict the 2000 pollen season; in addition, and in view of the heavy rainfall recorded in spring 2000, the 1982–1998 data set was used to test the model for 1999. The results of the multiple regression analysis show that the variables exerting the greatest influence on the pollen index were rainfall in March and temperatures over the months prior to the flowering period. For prediction of maximum values and dates on which these values might be expected, the start of the pollen season was used as an additional independent variable. Temperature proved the best variable for this prediction. Results improved when the 5-day moving average was taken into account. Testing of the predictive model for 1999 and 2000 yielded fairly similar results. In both cases, the difference between expected and observed pollen data was no greater than 10%. However, significant differences were recorded between forecast and expected maximum and minimum values, owing to the influence of rainfall during the flowering period.