Skip to main content Accessibility help
×
Hostname: page-component-cd9895bd7-hc48f Total loading time: 0 Render date: 2024-12-22T21:53:45.036Z Has data issue: false hasContentIssue false

2 - Pollination crisis, plant sex systems, and predicting evolutionary trends in attractiveness

Published online by Cambridge University Press:  05 January 2012

Sébastien Patiny
Affiliation:
Université de Mons-Hainaut, Belgium
Get access

Summary

Introduction

Since publication of The Forgotten Pollinators by Buchmann and Nabhan (1997), the term pollination crisis has gained widespread currency. Catchy phrases like “silent springs” and “fruitless falls” have been adopted in both the scientific literature and newspapers. Sub-optimal pollination of crops incurs an economic cost; less pollination may also lead to profound changes in the species composition of ecosystems all over the world. However, Aizen et al. (2008) have recently challenged the related idea that colonies of honeybees are generally on the decline (Jacobsen 2008). Analyzing data obtained from the FAO, they noted a downward trend in the number of bee colonies in Europe and North America, but an upward trend in non-industrialized countries that more than compensated for the decline. While this is good news, it is not the whole story. Aizen et al. (2008) also noted a trend in the crops that are being grown. Traditionally, wind-pollinated grains (rice, maize, wheat, rye) make up most of the world’s food supply. Now, insect-pollinated crops are on the rise – crops like Brazil nut, cocoa bean and oil palm. This creates a need for more honeybee colonies or other alternative pollinators, which is a challenge for the future. In this context it is useful to reflect on the likely effects of reduced pollination levels on natural ecosystems. Here I shall focus on plant sex systems and plant attractiveness in the context of reduced pollinator visitation, approaching the problem in the context of what is known about the evolutionary ecology of plants.

Expected effects of reduced pollination: dioecy and gynodioecy

The great majority of angiosperm species have perfect flowers. These flowers have both male parts that bear pollen, and female parts that receive pollen and later produce fruits and seeds. Combining the two sexes into a single flower is economic, sharing the costs of pollinator attraction and reward over the two sex functions. The proximity of the male and female organs has dual consequences, however. In plants that are self-compatible (SC), when pollinators are in short supply, selfing provides reproductive assurance, and this can be positive. Proximity may also be negative, though, when self-pollen on the stigma prevents outcrossing and reduces seed set, even in self-incompatible (SI) species (Webb and Lloyd 1986; Bertin 1993). These negative effects are known as pollen–stigma interference or pollen–pistil interference.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Aizen, M. A.Harder, L. D. 2007 Expanding the limits of the pollen-limitation concept: effects of pollen quantity and qualityEcology 88 271CrossRefGoogle ScholarPubMed
Aizen, M. A.Garibaldi, L. A.Cunningham, S. A.Klein, A. M. 2008 Long-term global trends in crop yield and production reveal no current pollination shortage but increasing pollinator dependencyCurrent Biology 18 1572CrossRefGoogle ScholarPubMed
Ashman, T. L. 2000 Pollinator selectivity and its implications for the evolution of dioecy and sexual dimorphismEcology 81 2577CrossRefGoogle Scholar
Ashman, T. L.Schoen, D. J. 1994 How long should flowers live?Nature 371 788CrossRefGoogle Scholar
Barrett, S. C. H. 2003 Mating strategies in flowering plants: the outcrossing-selfing paradigm and beyondPhilosophical Transactions of the Royal Society B, Biological Sciences 358 991CrossRefGoogle ScholarPubMed
Barrett, S. C. H. 2010 Darwin’s legacy: the forms, function and sexual diversity of flowersPhilosophical Transactions of the Royal Society B, Biological Sciences 365 351CrossRefGoogle ScholarPubMed
Bell, G. 1985 On the function of flowersProceedings of the Royal Society London B 224 223CrossRefGoogle Scholar
Bell, S. A.Creswell, J. E. 1998 The phenology of gender in homogamous flowers: temporal change in the residual sex function of oilseed rapeOikos 98 375Google Scholar
Bertin, R. I. 1993 Incidence of monoecy and dichogamy in relation to self-fertilization in AngiospermsAmerican Journal of Botany 80 557CrossRefGoogle Scholar
Buchmann, S. L.Nabhan, G. P. 1997 The Forgotten PollinatorsWashington, DCIsland Press.Google Scholar
Burd, M. 1994 Bateman’s principle and plant reproduction: the role of pollen limitation in fruit and seed setBotanical Review 60 83CrossRefGoogle Scholar
Cohen, D.Shmida, A. 1993 The evolution of flower display and rewardEvolutionary Biology 27 197Google Scholar
Carlson, J. E. 2007 Male-biased nectar production in a protandrous herb matches predictions of sexual selection theoryAmerican Journal of Botany 94 674CrossRefGoogle Scholar
Carlson, J. E.Harms, K. E. 2006 The evolution of gender-biased production in hemaphrodite plantsBotanical Review 72 179CrossRefGoogle Scholar
Charlesworth, D. 1985 Evolution: Essays in Honour of John Maynard SmithP. J. Greenwood, P. H. HarveySlatkin, M.Cambridge, MACambridge University PressGoogle Scholar
Charnov, E. L.Bull, J. J. 1986 Sex allocation, pollinator attraction and fruit dispersal in cosexual plantsJournal of Theoretical Biology 118 321CrossRefGoogle Scholar
Darwin, C. 1877 The Different Forms of Flowers on Plants of the Same SpeciesLondon, UKMurrayCrossRefGoogle Scholar
Darwin, C. 1878 The Effect of Cross- and Self-Fertilization in the Vegetable KingdomLondon, UKPickeringCrossRefGoogle Scholar
Delesalle, V. A.Muenchow, G. E. 1992 Opportunities for selfing and inbreeding depression in congeners (Alismataceae) with contrasting sexual systemsEvolutionary Trends in Plants 6 81Google Scholar
Dorken, M. E.Friedman, J.Barrett, S. C. H. 2002 The evolution and maintenance of monoecy and dioecy in (Alismataceae)Ecology 56 31Google Scholar
Fisher, R. A. 1930 The Genetical Theory of Natural SelectionOxford, UKClarendon PressCrossRefGoogle Scholar
Fishman, L.Willis, J. H. 2008 Pollen limitation and natural selection on floral characters in the yellow monkeyflower, New Phytologist 177 802CrossRefGoogle Scholar
Ganeshaiah, K. N.Shaanker, R. U. 1991 Floral sex-ratios in monoecious species: why are trees more male-biased than herbs?Current Science 60 319Google Scholar
Haig, D.Westoby, M. 1988 On limits to seed productionAmerican Naturalist 131 757CrossRefGoogle Scholar
Jacobsen, R. 2008 Fruitless Fall: the Collapse of the Honeybee and the Coming Agricultural CrisisLondon, UKBloomsbury PublishingGoogle Scholar
de Jong, T. J.Klinkhamer, P. G. L. 2005 Evolutionary Ecology of Plant Reproductive StrategiesCambridge, UKCambridge University PressGoogle Scholar
de Jong, T. J.Batenburg, J. C.Klinkhamer, P. G. L. 2005 Distance-dependent pollen limitation of seed set in some insect-pollinated dioecious plantsActa oecologia 28 331CrossRefGoogle Scholar
de Jong, T. J.Shmida, A.Thuijsman, F. 2008 Sex allocation in plants and the evolution of monoecyEvolutionary Ecology Research 10 1087Google Scholar
Kawagoe, T.Suzuki, N. 2005 Self-pollen on a stigma interferes with outcrossed seed production in a self-incompatible monoecious plantAkebia quinata 19 49Google Scholar
Klinkhamer, P. G. L.de Jong, T. J.Linnenbank, L. A. 2001 Small-scale spatial patterns determine ecological relationships: an experimental example using nectar production ratesEcology Letters 4 559CrossRefGoogle Scholar
Kobuta, S.Ohara, M. 2009 Discovery of male sterile plants and their contrasting occurrence between self-compatible and self-incompatible populations of the hermaphroditic perennial Plant Species Biology 24 169CrossRefGoogle Scholar
Lloyd, D. G. 1975 The maintenance of gynodioecy and androdioecy in angiospermsGenetica 45 325CrossRefGoogle Scholar
Miller, J. S.Diggle, P. K. 2007 Correlated evolution of fruit size and sexual expression in andromonoecious sections and (Solanaceae)American Journal of Botany 94 1706CrossRefGoogle Scholar
Mitchell, C. H.Diggle, P. K. 2005 Evolution of unisexual flowers: morphological and functional convergence results from diverse developmental transitionsAmerican Journal of Botany 92 106876CrossRefGoogle ScholarPubMed
Mitchell, R. J.Ashman, T. L. 2008 Predicting evolutionary consequences of pollinator declines: the long and short of floral evolutionNew Phytologist 177 576CrossRefGoogle Scholar
Mitchell, R. J.Flanagan, R. J.Brown, B. J.Waser, N. M.Karron, J. D. 2009 New frontiers in competition for pollinationAnnals of Botany 103 1403CrossRefGoogle ScholarPubMed
Schoen, D. J.Ashman, T. L. 1995 The evolution of floral longevity: resource allocation to maintenance versus construction of repeated parts in modular organismsEvolution 49 131CrossRefGoogle ScholarPubMed
Spalik, K. 1991 On evolution of andromonoecy and “overproduction” of flowers: a resource allocation modelBiological Journal of the Linnean Society 42 325CrossRefGoogle Scholar
Stanton, M. L.Snow, A. A.Handel, S. N. 1986 Floral evolution: attractiveness to pollinators increases male fitnessScience 232 1625CrossRefGoogle ScholarPubMed
Vaughton, G.Ramsey, M. 2010 Floral emasculation reveals pollen quality limitation of seed output in American Journal of Botany 97 174CrossRefGoogle Scholar
Webb, C. J.Lloyd, D. G. 1986 The avoidance of interference between the presentation of pollen and stigma in AngiospermsNew Zealand Journal of Botany 24 163CrossRefGoogle Scholar
Wilson, P.Thomson, J. C.Stanton, M. L.Rigney, L. P. 1994 Beyond floral Batemania: gender biases in selection for pollination successAmerican Naturalist 143 283CrossRefGoogle Scholar

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×