scholarly journals Male flowers of Aconitum compensate for toxic pollen with increased floral signals and rewards for pollinators

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
A.-L. Jacquemart ◽  
C. Buyens ◽  
M.-F. Hérent ◽  
J. Quetin-Leclercq ◽  
G. Lognay ◽  
...  
Keyword(s):  
Larval Food ◽  
Chemical Defences ◽  
Toxic Nectar ◽  
Pollen Transfer Efficiency ◽  
Aconitum Napellus ◽  
Female Phase ◽  
Male Phase ◽  
Male Flowers ◽  
Nectar Rewards ◽  
Toxic Pollen

Abstract Many plants require animal pollinators for successful reproduction; these plants provide pollinator resources in pollen and nectar (rewards) and attract pollinators by specific cues (signals). In a seeming contradiction, some plants produce toxins such as alkaloids in their pollen and nectar, protecting their resources from ineffective pollinators. We investigated signals and rewards in the toxic, protandrous bee-pollinated plant Aconitum napellus, hypothesizing that male-phase flower reproductive success is pollinator-limited, which should favour higher levels of signals (odours) and rewards (nectar and pollen) compared with female-phase flowers. Furthermore, we expected insect visitors to forage only for nectar, due to the toxicity of pollen. We demonstrated that male-phase flowers emitted more volatile molecules and produced higher volumes of nectar than female-phase flowers. Alkaloids in pollen functioned as chemical defences, and were more diverse and more concentrated compared to the alkaloids in nectar. Visitors actively collected little pollen for larval food but consumed more of the less-toxic nectar. Toxic pollen remaining on the bee bodies promoted pollen transfer efficiency, facilitating pollination.

Pollination of Amorphophallus johnsonii (Araceae) by carrion beetles (Phaeochrous amplus) in a Ghanaian rain forest

1996 ◽  
Vol 12 (3) ◽  
pp. 409-418 ◽  
Author(s):  
Daniel D. N. Beath
Keyword(s):  
Rain Forest ◽  
Rainy Season ◽  
Male Inflorescence ◽  
Large Numbers ◽  
Female Phase ◽  
Male Phase ◽  
Carrion Beetles ◽  
Main Rainy Season

ABSTRACTAmorphophallus johnsonii (N. E. Brown) flowers during April in the main rainy season in Ghana. Anthesis starts at dusk with fluid oozing from the upper spadix accompanied by a strong aminoid odour. Just after dark large numbers of carrion beetles (Phaeochrous amplus) and occasional dung fly species (Hemigymnochaeta unicolor and Paryphodes tigrinus) visit the inflorescences. The beetles become trapped in the lower spathe overnight and remain in the spadix until the following evening. Between 1630 and 1645 h the following day, the anthers produce long threads of sticky pollen. The trapped beetles escape just after dark by crawling up the spadix, past the dehisced anthers and fly away from the spadix tip. Marked beetles were seen to transfer pollen from male phase to female phase inflorescences. Successful fertilisation was only effected if pollen was transferred on the same night from a male inflorescence 30 m or less away. Pollen is psilate and typical of beetle pollinated Araceae. Berries ripen approximately 70 d after fertilization and ripen basisetally in the infructescence.

scholarly journals Linking pollinator efficiency to patterns of pollen limitation: small bees exploit the plant–pollinator mutualism

2018 ◽  
Vol 285 (1880) ◽  
pp. 20180635 ◽  
Author(s):  
Matthew H. Koski ◽  
Jennifer L. Ison ◽  
Ashley Padilla ◽  
Angela Q. Pham ◽  
Laura F. Galloway
Keyword(s):  
Pollen Limitation ◽  
Pollen Deposition ◽  
Pollinator Efficiency ◽  
Flower Visitation ◽  
Female Phase ◽  
Male Phase ◽  
Single Flower ◽  
Floral Visitation ◽  
Low Efficiency ◽  
Plant Pollinator

Seemingly mutualistic relationships can be exploited, in some cases reducing fitness of the exploited species. In plants, the insufficient receipt of pollen limits reproduction. While infrequent pollination commonly underlies pollen limitation (PL), frequent interactions with low-efficiency, exploitative pollinators may also cause PL. In the widespread protandrous herb Campanula americana , visitation by three pollinators explained 63% of the variation in PL among populations spanning the range. Bumblebees and the medium-sized Megachile campanulae enhanced reproductive success, but small solitary bees exacerbated PL. To dissect mechanisms behind these relationships, we scored sex-specific floral visitation, and the contributions of each pollinator to plant fitness using single flower visits. Small bees and M. campanulae overvisited male-phase flowers, but bumblebees frequently visited female-phase flowers. Fewer bumblebee visits were required to saturate seed set compared to other bees. Scaling pollinator efficiency metrics to populations, small bees deplete large amounts of pollen due to highly male-biased flower visitation and infrequent pollen deposition. Thus, small bees reduce plant reproduction by limiting pollen available for transfer by efficient pollinators, and appear to exploit the plant–pollinator mutualism, acting as functional parasites to C. americana . It is therefore unlikely that small bees will compensate for reproductive failure in C. americana when bumblebees are scarce.

scholarly journals Intraspecific Seasonal Variation of Flowering Synchronization in a Heterodichogamous Tree

Plants ◽  
2020 ◽  
Vol 9 (11) ◽  
pp. 1509
Author(s):  
Noemi Tel-Zur ◽  
Tamar Keasar
Keyword(s):  
Genetic Diversity ◽  
Seasonal Variation ◽  
Phase Duration ◽  
Male And Female ◽  
Flowering Synchrony ◽  
Flowering Season ◽  
Hand Pollination ◽  
Female Phase ◽  
Male Phase ◽  
Phase Differences

Heterodichogamous reproduction in plants involves two flowering morphs, reciprocal in their timing of male and female sexual functions. The degree of synchrony in floral sex phase, within and between individuals of each morph, determines the flowers’ potential fertilization partners. Complete within-morph synchrony enables across-morph mating alone, whereas unsynchronized floral sex phases may allow fertilization within a plant individual (geitonogamy) or within a morph. We documented the disruption of flowering synchrony in the heterodichogamous Ziziphus spina-christi towards the end of its seven-month flowering season. This desert tree has self-incompatible, protandrous, short-lived (2-day) flowers that open before dawn (‘Early’ morph) or around noon (‘Late’ morph). We counted flowers in the male and female phase on flowering branches that were sampled monthly during the 2016–2018 flowering seasons. In 2018, we also tagged flowers and followed their sex-phase distributions over two days at the start, middle, and end of the season. The switch to the female phase was delayed at the end-season (November-December), and 74% of the flowers did not develop beyond their male phase. Differences in male-phase duration resulted in asynchrony among flowers within each tree and among trees of both flowering morphs. Consequently, fertilization between trees of the same morph becomes potentially possible during the end-season. In controlled hand-pollination assays, some within-morph fertilizations set fruit. The end-season breakdown of synchronous flowering generates variability within morphs and populations. We suggest that this variability may potentially enable new mating combinations in a population and enhance its genetic diversity.

scholarly journals Nectar secretion and pollen production in protandrous flowers of Campanula patula L. (Campanulaceae)

2018 ◽  
Vol 71 (1) ◽  
Author(s):  
Bożena Denisow ◽  
Monika Strzałkowska-Abramek ◽  
Małgorzata Wrzesień
Keyword(s):  
Sugar Accumulation ◽  
Reproductive Costs ◽  
Pollen Production ◽  
Nectar Secretion ◽  
Mass Content ◽  
Plastic Response ◽  
Male And Female ◽  
Functional Relationships ◽  
Female Phase ◽  
Male Phase

Nectar secretion was noted both in the male and female floral phases of the protandrous flowers of <em>Campanula patula</em> (Campanulaceae). Female-biased sugar accumulation was evidenced and plasticity in the duration of sexual phases observed. Flowers in the male phase produced twofold less nectar with lower sugar concentrations compared to female-phase flowers. The sugar mass content averaged 0.6 mg ±0.45 <em>SD</em> per flower in the male phase and 1.4 ±0.5 <em>SD</em> per flower in the female phase. The pollen mass averaged 0.16 mg ±0.10 <em>SD</em> per flower. An understanding of the evolution of functional relationships between floral sexes requires consideration of the compensation of the reproductive costs, including the plastic response to interdependent factors, i.e., photosynthesis and growth, the effect of pollinators, pollen robbers, and external environmental forces.

Within and among flower sex-phase distribution in Alstroemeria aurea (Alstroemeriaceae)

1995 ◽  
Vol 73 (12) ◽  
pp. 1986-1994 ◽  
Author(s):  
Marcelo A. Aizen ◽  
Alicia Basilio
Keyword(s):  
Inbreeding Depression ◽  
Seed Set ◽  
Phase Distribution ◽  
Selfing Rate ◽  
Pollen Transfer ◽  
Alstroemeria Aurea ◽  
Female Phase ◽  
Male Phase ◽  
Male To Female ◽  
Simultaneous Change

Although dichogamy is a prevailing feature of the angiosperms, the simultaneous change from male to female phases among hermaphrodite flowers within a plant (i.e., synchronous protandry) has been reported for only a few families (e.g., Araliaceae, Umbelliferae). Here we present an example of synchronous protandry at the ramet level in the Alstroemeriaceae. Dichogamy was analyzed in clonal Alstroemeria aurea at the flower, ramet, and at the whole flowering patch level. Alstroemeria aurea is self-compatible but totally dependent on biotic agents for pollen transfer. There was evidence of strong inbreeding depression expressed during seed development. Comparisons of seed set in open-pollinated flowers with those obtained after hand selfing and outcrossing resulted in a selfing rate of 0.3. At the flower level protandry was complete. The male phase lasted about 4 days and the female phase lasted about 3 days. Between the female and male phase, there was an approximately 1-day long "neuter" phase. Flowering ramets produce a terminal inflorescence bearing one or more whorls of flowers. Within a ramet, flowers of the same order opened within a period of 1–2 days, and male and female phases of different flowers did not overlap. When inflorescences held two whorls of flowers, the ramet went through two alternating non-overlapping male–female cycles. Using spatial autocorrelation techniques, we found little evidence for pairs of neighboring ramets expressing the same sexual phase beyond random expectations at any scale ranging between 0.25 to 15 m. By ensuring pollen interchange between flowering ramets, synchronized protandry at the ramet level could be an important feature in reducing selfing in A. aurea. Key words: Alstroemeria aurea, dichogamy, synchronous protandry, inbreeding depression.

Primary Sex-Phases in Ostrea Edulis

1942 ◽  
Vol s2-83 (331) ◽  
pp. 317-356
Author(s):  
H. A. COLE
Keyword(s):  
Water Temperature ◽  
Environmental Conditions ◽  
Initial Phase ◽  
Gonad Development ◽  
Ostrea Edulis ◽  
Male Condition ◽  
Female Phase ◽  
Male Phase ◽  
One Year ◽  
Transitional Phase

1. It is only under the most favourable conditions that oysters (Ostrea edulis) mature in the first sexual phase in the same season as that in which they attach themselves. During this initial phase the oyster functions as a male. 2. Normally the first male phase is experienced on British beds in the summer following that in which the oyster attaches itself and is rapidly followed by the first female phase, the oocytes developing on the walls of the follicles while spermatogenesis proceeds in the lumina. 3. In favourable seasons about a third of a population of one-year-old oysters will spawn as females. In unfavourable years only a few of the heaviest oysters spawn. Following female spawning the second male phase is rapidly assumed. 4. The second male phase is followed by the second female phase, the oocytes developing while spermatogenesis is in progress. Emission of sperm may be continued up to within a few days of egg-spawning. If a male phase is reached towards the close of the season it is followed by a resting phase, without spermatogenesis or large oocytes in the gonad, which persists throughout the winter. Similar resting phases may occur during the summer if environmental conditions are unfavourable. 5. Every two-year-old oyster functions as a female in a favourable season, and thereafter under normal conditions passes through at least two sex-phases each season, functioning both as a male and as a female. Evidence is adduced to show that in populations of adult oysters on British beds 100 per cent, female functioning occurs in favourable seasons. 6. Gonad development is arrested from approximately the end of October until the beginning of April while the water temperature is below about 10°C. Oysters may winter in almost any sex-phase, but spermatogenesis does not occur, although ripe sperm morulae may be carried over from one season to the next. Egg development is arrested during the winter months. 7. Oysters which winter in a transitional phase between a male and a female phase may mature as pure females early in the following summer without any recrudescence of spermatogenesis. There is at this time, therefore, a high proportion of ripe females in the population. 8. Oysters which winter in a dormant male condition mature as good males early in the following season and spawn as females later in the summer. Female spawners may therefore be divided roughly into two groups--early and late spawners--and individual oysters tend to remain in the same group in successive years. 9. Breakdown and absorption of large eggs by phagocytes has been found to occur occasionally during the winter, but the circumstances in which this takes place are not known.

Thermogenesis in Syngonium (Araceae)

2007 ◽  
Vol 85 (2) ◽  
pp. 184-190 ◽  
Author(s):  
Mathieu Chouteau ◽  
Denis Barabé ◽  
Marc Gibernau
Keyword(s):  
Heat Production ◽  
Stigma Receptivity ◽  
The Third ◽  
Female Phase ◽  
Male Phase

Floral cycles and spadix temperatures were recorded for two species of Syngonium: Syngonium schottianum Wendl. ex Schott (section Cordatum) and Syngonium angustatum Schott (section Syngonium). Both species exhibited a 3-day flowering cycle, beginning with stigma receptivity and opening of the spathe the first day, the female phase continues over the second day, and the male phase continues over the third day. These species displayed two distinct patterns of heat production during flowering. In S. schottianum, the spadix warmed up twice during the beginning of the second and third nights, but in S. angustatum, the spadix warmed up twice the second day, once the second night, and once the third day. These different thermogenic cycles are discussed in regard to other genera that are phylogenetically close or sharing similar flowering and thermogenic cycles.

Respiration and temperature patterns in thermogenic flowers of Magnolia ovata under natural conditions in Brazil

2010 ◽  
Vol 37 (9) ◽  
pp. 870 ◽  
Author(s):  
Roger S. Seymour ◽  
Ilse Silberbauer-Gottsberger ◽  
Gerhard Gottsberger
Keyword(s):  
Ambient Temperature ◽  
Respiration Rate ◽  
Energy Savings ◽  
Ambient Air ◽  
Pollination Biology ◽  
Specific Rate ◽  
Maximum Mass ◽  
Natural Conditions ◽  
Female Phase ◽  
Male Phase

The roles of floral thermogenesis in pollination biology include attraction and reward of insects. Magnolia ovata (A.St.-Hil.) Spreng. produces ~56 g, bisexual, protogynous and scented flowers. Two distinct episodes of thermogenesis occur during anthesis: one beginning at about sunset and lasting ~3 h in the female phase and another that occurs synchronously 24 h later and lasting 4 h in the male phase. Female stage flowers produce up to 0.36 W to reach 27.3°C, which is 3.9°C above ambient air. In the male stage, corresponding values are 0.79 W, 29.7°C and 5.4°C, respectively. Most heat is generated in the petals in both phases (74 and 65%). Maximum, mass-specific rate of respiration is 23 nmol s–1 g–1 in the petals and 100 nmol s–1 g–1 in the anthers. The flowers are apparently not thermoregulatory, because respiration rate decreases, rather than increases, with decreasing ambient temperature. Scarab beetles, Cyclocephala literata, enter the floral chamber created by the petals in the female phase, mate, consume floral parts (mainly petals) and then depart in the male phase. Temperatures maintained in the floral chamber are sufficient to provide beetles with significant energy savings during their activities in both phases. Thermogenesis is, therefore, consistent with volatilisation of floral fragrances and energy rewards to beetle visitors.

Nectar secretion pattern, removal effects, and breeding system of Ligaria cuneifolia (Loranthaceae)

1996 ◽  
Vol 74 (12) ◽  
pp. 1996-2001 ◽  
Author(s):  
Guillermo L. Rivera ◽  
Leonardo Galetto ◽  
L. Bernardello
Keyword(s):  
Reproductive Biology ◽  
Breeding System ◽  
Nectar Production ◽  
Female Function ◽  
Flower Nectar ◽  
Flower Age ◽  
Female Phase ◽  
Male Phase ◽  
Pattern Removal ◽  
Flower Phenology

Some aspects of the reproductive biology of Ligaria cuneifolia have been studied, addressing the following questions: (i) Are there temporal differences in the female and male functions? (ii) How do nectar composition, volume, concentration, and amount of sugar vary throughout the flower lifetime? (iii) How does the plant respond to nectar removal? (iv) What is the breeding system of this species? Flowers last 4 days. There is a predominance of the male function in the first days and of the female function in the last days. Chemical composition of nectar varies throughout the flower lifetime; there is a constant decrease in sucrose along with an increase in glucose. Nectar is secreted during nights, and every secretion period is followed by a cessation interval. After the final cessation, a period of active resorption follows. During the mostly male phase of the flower, nectar has more sucrose than hexose, its secretion is discontinuous, and nectar removal reduces the rate of nectar production. During the mostly female phase, nectar has more hexose than sucrose, its secretion ceases, nectar removal does not affect nectar production, and a resorption period is inferred. Tests for spontaneous autogamy and apomixis were negative. Low fruit set is obtained when autogamous, geitonogamous, and xenogamous hand pollinations are performed on flowers less than 2 days old compared with flowers at least 3 days old (0, 15, and 47% versus 19, 37.5, and 89%, respectively). These results indicate the the reproductive system of L. cuneifolia is primarily xenogamous, but reproductive success is related to flower age. Keywords: Loranthaceae, Ligaria, nectar chemistry, breeding system, flower phenology, reproductive biology.

scholarly journals Accurate position exchange of stamen and stigma by movement in opposite direction resolves the herkogamy dilemma in a protandrous plant, Ajuga decumbens (Labiatae)

AoB Plants ◽  
2019 ◽  
Vol 11 (5) ◽  
Author(s):  
Zhong-Ming Ye ◽  
Xiao-Fang Jin ◽  
Jian Yang ◽  
Qing-Feng Wang ◽  
Chun-Feng Yang
Keyword(s):  
Pollen Viability ◽  
Floral Biology ◽  
Pollen Deposition ◽  
High Viability ◽  
Pollen Removal ◽  
Female Phase ◽  
Male Phase ◽  
Accurate Position ◽  
Sexual Interference ◽  
Position Exchange

Abstract Herkogamy is an effective way to reduce sexual interference. However, the separation of stigma and anther potentially leads to a conflict because the pollen may be placed in a location on the pollinator different from the point of stigma contact, which can reduce pollination accuracy. Floral mechanisms aiming to resolve this conflict have seldom been explored. The floral biology of protandrous Ajuga decumbens was studied to uncover how the herkogamy dilemma can be resolved. Flower anthesis was divided into male, middle, female and wilting phases. The positions of stigma and stamen were dissimilar in different flower development stages. We measured the distance of the stamen and stigma to the lower corolla lip at different floral phases, which was the pollinators’ approaching way. The pollen viability, stigma receptivity, pollen removal and pollen deposition on stigma were investigated at different phases. During the male phase, the dehisced anthers were lower than the stigma, located at the pollinators’ approaching way, and dispersed most pollen with high viability. As the flower developed, the anthers moved upwards, making way for pollen deposition during the female phase. Meanwhile, the stigma becomes receptive by moving into the way and consequently was deposited with sufficient pollen. The position exchange of the stamen and stigma created a dynamic herkogamy at the floral phase with different sexual functions. This floral mechanism effectively avoided sexual interference and maintained pollination accuracy. In Ajuga, the movement herkogamy might be of adaptive significance in response to the changes in the pollination environment.

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