Literature DB >> 28311646

The pollination biology and breeding system of Monarda fistulosa (Labiatae).

Robert William Cruden1, Luise Hermanutz1, Jane Shuttleworth1.   

Abstract

Successful cross-pollination of Monarda fistulosa is the result of a complex interaction among flower opening, the pollen-bearing areas of the pollinators and/or their behavior, and the maturation of the stigmas. The flowers open continuously from 0800-2000 h providing a temporally predictable rich source of nectar and pollen. Recently opened flowers may reduce the ability of bees to discriminate between resource rich and poor patches and encourage systematic foraging within patches. The continuous opening of flowers coupled with protandry also results in some flowers of most capitula being in the staminate and others in the pistillate phase. Autogamy is highly unlikely due to strong protandry and the spatial separation of anthers and stigmas. Geitonogamy, at least that mediated by Bombus is unlikely because the pollen is spread over a relatively large area of the wings, which reduces the likelihood of a stigma contacting just deposited pollen. Because pollen is transferred from the much smaller coxal area of Anthophora and other bees that mistake the stigmas of early pistillate phase flowers for stamens some geitonogamy seems inevitable. However, the delayed receptivity of young stigmas to self-pollen decreases the likelihood of self-pollen germinating on such stigmas. Older stigmas are equally receptive to self- and cross-pollen and the number of pollen grains germinating and pollen tubes reaching the base of the style increases with flower age.

Entities:  

Year:  1984        PMID: 28311646     DOI: 10.1007/BF00377551

Source DB:  PubMed          Journal:  Oecologia        ISSN: 0029-8549            Impact factor:   3.225


  13 in total

1.  Staining and observing pollen tubes in the style by means of fluorescence.

Authors:  F W MARTIN
Journal:  Stain Technol       Date:  1959-05

2.  Pollinators in high-elevation ecosystems: relative effectiveness of birds and bees.

Authors:  R W Cruden
Journal:  Science       Date:  1972-06-30       Impact factor: 47.728

Review 3.  The physiology of the pollen grain surface.

Authors:  J Heslop-Harrison
Journal:  Proc R Soc Lond B Biol Sci       Date:  1975-08-19

4.  On the calculation of sugar concentration in flower nectar.

Authors:  Alan B Bolten; Peter Feinsinger; Herbert G Baker; Irene Baker
Journal:  Oecologia       Date:  1979-08       Impact factor: 3.225

5.  Patchiness in the dispersion of nectar resources: Evidence for hot and cold spots.

Authors:  John M Pleasants; Michael Zimmerman
Journal:  Oecologia       Date:  1979-08       Impact factor: 3.225

6.  CRYPTIC SELF-INCOMPATIBILITY IN AMSINCKIA GRANDIFLORA.

Authors:  Stephen G Weller; Robert Orndufe
Journal:  Evolution       Date:  1977-03       Impact factor: 3.694

7.  POLLINATION BIOLOGY OF NEMOPHILA MENZIESII (HYDROPHYLLACEAE) WITH COMMENTS ON THE EVOLUTION OF OLIGOLECTIC BEES.

Authors:  Robert William Cruden
Journal:  Evolution       Date:  1972-09       Impact factor: 3.694

8.  TEMPORAL DIOECISM: AN ALTERNATIVE TO DIOECISM?

Authors:  Robert William Cruden; Sharon Marie Hermann-Parker
Journal:  Evolution       Date:  1977-12       Impact factor: 3.694

9.  Optimal foraging: movement patterns of bumblebees between inflorescences.

Authors:  G H Pyke
Journal:  Theor Popul Biol       Date:  1978-02       Impact factor: 1.570

10.  Patchiness in the dispersion of nectar resources: Probable causes.

Authors:  Michael Zimmerman
Journal:  Oecologia       Date:  1981-05       Impact factor: 3.225

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  1 in total

1.  How and why do nectar-foraging bumblebees initiate movements between inflorescences of wild bergamot Monarda fistulosa (Lamiaceae)?

Authors:  James E Cresswell
Journal:  Oecologia       Date:  1990-04       Impact factor: 3.225

  1 in total

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