Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-pftt2 Total loading time: 0 Render date: 2024-05-30T20:10:03.235Z Has data issue: false hasContentIssue false

Chapter 5 - Towards the next generation: flowers, fruits and seeds

Published online by Cambridge University Press:  05 July 2014

Peter A. Thomas
Affiliation:
Keele University
Get access

Summary

Like other plants, trees have to engage in sex by proxy, using the wind, water or an animal as an intermediary to get pollen from one tree to another (see Box 5.1). Unlike many other plants, the sheer size of trees raises extra problems of pollination, and eventually seed dispersal, which are solved in ingenious ways. The original trees, the conifers, were (and still are) wind-pollinated. The flowering plants (angiosperms), which includes hardwood trees, evolved hand in hand with insects to be, not surprisingly, primarily insect-pollinated. Yet some have reverted to the old way of wind pollination, and for very good reasons. These are linked to geography: most trees in high latitudes are wind-pollinated, but animal pollination (insects, birds and mammals) becomes more important the closer one gets to the tropics, reaching 95% of trees around the equator. Figure 5.1 gives an overview of general flower structure.

Animal pollination

Animal pollination is primarily the world of the insect; in the wettest Costa Rican forests, for example, 90% of trees are insect pollinated. But within insect pollination there are different strategies. Some trees, like magnolias, apples, rowan (Sorbus aucuparia), European spindle (Euonymus europaea), some maples, hawthorns (Crataegus spp.) and a long list of others, go for quantity. They are generalists that spread the pollen on a wide range of flies and beetles in the hope that some will arrive on another flower of the same species. Common features are open flowers, often facing upwards, a drab colour, many stamens, easily reached nectar and a strong scent, especially at night (see Box 5.2 and Figure 5.2).

Type
Chapter
Information
Trees
Their Natural History
, pp. 154 - 204
Publisher: Cambridge University Press
Print publication year: 2014

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

Ashton, P.S., Givnish, T.J. & Appanah, S. (1988) Staggered flowering in the Dipterocarpaceae: new insights into floral induction and the evolution of mast flowering in the aseasonal tropics. American Naturalist, 132, 44–66.CrossRefGoogle Scholar
Bazzaz, F.A., Carlson, R.W. & Harper, J.L. (1979) Contribution to reproductive effort by photosynthesis of flowers and fruits. Nature, 279, 554–555.CrossRefGoogle Scholar
Borchert, R., Renner, S.S., Calle, Z. et al. (2005) Photoperiodic induction of synchronous flowering near the equator. Nature, 433, 627–629.CrossRefGoogle ScholarPubMed
Camarero, J.J., Albuixech, J., López-Lozano, R., Casterad, M.A. & Montserrat-Martı, G. (2010) An increase in canopy cover leads to masting in Quercus ilex. Trees, 24, 909–918.CrossRefGoogle Scholar
Dick, J. McP., Leakey, R.R.B. & Jarvis, P.G. (1990) Influence of female cones on the vegetative growth of Pinus contorta trees. Tree Physiology, 6, 151–163.CrossRefGoogle ScholarPubMed
Drobyshev, I., Övergaard, R., Saygin, I., et al. (2010) Masting behaviour and dendrochronology of European beech (Fagus sylvatica L.) in southern Sweden. Forest Ecology and Management, 259, 2160–2171.CrossRefGoogle Scholar
Greene, D.F., Quesada, M. & Calogeropoulos, C. (2008) Dispersal of seeds by the tropical sea breeze. Ecology, 89, 118–125.CrossRefGoogle ScholarPubMed
Horsley, T.N. & Johnson, S.D. (2007) Is Eucalyptus cryptically self-incompatible?Annals of Botany, 100, 1373–1378.CrossRefGoogle ScholarPubMed
Janzen, D.H. (1971) Seed predation by animals. Annual Review of Ecology and Systematics, 2, 465–492.CrossRefGoogle Scholar
Kay, Q.O.N. (1985) Nectar from willow catkins as a food source for Blue Tits. Bird Study, 32, 40–45.CrossRefGoogle Scholar
Kikuchi, S., Shibata, M., Tanaka, H., Yoshimaru, H. & Niiyama, K. (2009) Analysis of the disassortative mating pattern in a heterodichogamous plant, Acer mono Maxim. using microsatellite markers. Plant Ecology, 204, 43–54.CrossRefGoogle Scholar
Kislev, M.E., Hartmann, A. & Bar-Yosef, O. (2006) Early domesticated fig in the Jordan Valley. Science, 312, 1372–1374.CrossRefGoogle ScholarPubMed
Kowarik, I. & Säumel, I. (2008) Water dispersal as an additional pathway to invasions by the primarily wind-dispersed tree Ailanthus altissima. Plant Ecology, 198, 241–252.CrossRefGoogle Scholar
Lanner, R.M. (1996) Made for Each Other: a Symbiosis of Birds and Pines. Oxford University Press, Oxford.Google Scholar
Lee, W.Y., Lee, J.S., Lee, J.-H., Noh, E.W. & Park, E.-J. (2011) Enhanced seed production and metabolic alterations in Larix leptoepis by girdling. Forest Ecology and Management, 261, 1957–1961.CrossRefGoogle Scholar
Mellanby, K. (1968) The effects of some mammals and birds on regeneration of oak. Journal of Applied Ecology, 5, 359–366.CrossRefGoogle Scholar
Mitchell, A.M. (1974) A Field Guide to the Trees of Britain and Northern Ireland. Collins, London.Google Scholar
Mitchell, A.W. (1987) The Enchanted Canopy. Fontana, London.Google Scholar
Obeso, J.R. (1997) Costs of reproduction in Ilex aquifolium: effects at tree, branch and leaf levels. Journal of Ecology, 85, 159–166.CrossRefGoogle Scholar
Ohashi, K. & Thomson, J.D. (2007) Trapline foraging by pollinators: its ontogeny, economics and possible consequences for plants. Annals of Botany, 103, 1365–1378.CrossRefGoogle Scholar
Pichot, C., El Maâtaoui, M., Raddi, S. & Raddi, P. (2001) Surrogate mother for endangered Cupressus. Nature, 412, 39.CrossRefGoogle ScholarPubMed
Piggot, C.D. (1975) Natural regeneration of Tilia cordata in relation to forest structure in the forest of Białowieża. Philosophical Transactions of the Royal Society, Series B, 270, 151–179.CrossRefGoogle Scholar
Pons, J. & Pausas, J.G. (2007) Acorn dispersal estimated by radio-tracking. Oecologia, 153, 903–911.CrossRefGoogle ScholarPubMed
Queenborough, S.A., Mazer, S.J., Vamosi, S.M., et al. (2009) Seed mass, abundance and breeding system among tropical forest species: do dioecious species exhibit compensatory reproduction or abundances?Journal of Ecology, 97, 555–566.CrossRefGoogle Scholar
Silvertown, J.W. (1980) The evolutionary ecology of mast seeding in trees. Biological Journal of the Linnean Society, 14, 235–250.CrossRefGoogle Scholar
Silvertown, J. (2010) An Orchard Invisible, a Natural History of Seeds. University of Chicago Press, Chicago.Google Scholar
Soons, M.B. & Bullock, J.M. (2008) Non-random seed abscission, long-distance wind dispersal and plant migration rates. Journal of Ecology, 96, 581–590.CrossRefGoogle Scholar
Spigler, R.B. & Ashman, T.L. (2012) Gynodioecy to dioecy: are we there yet?Annals of Botany, 109, 531–543.CrossRefGoogle ScholarPubMed
Stephenson, A.G. (1981) Flower and fruit abortion: proximate causes and ultimate functions. Annual Review of Ecology and Systematics, 12, 253–279.CrossRefGoogle Scholar
Terry, I., Walter, G.H., Moore, C., Roemer, R. & Hull, C. (2007) Odor-mediated push-pull pollination in cycads. Science, 318, 70.CrossRefGoogle ScholarPubMed
Thomas, P.A., El-Barghathi, M. & Polwart, A. (2007) Biological Flora of the British Isles, Juniperus communis L. Journal of Ecology, 95, 1404–1440.CrossRefGoogle Scholar
Thomas, P.A., El-Barghathi, M. & Polwart, A. (2011) Biological Flora of the British Isles, Euonymus europaeus L. Journal of Ecology, 99, 345–365.CrossRefGoogle Scholar
Vander Wall, S.B. (1994) Removal of wind-dispersed pine seeds by ground-foraging vertebrates. Oikos, 69, 125–132.CrossRefGoogle Scholar
Vander Wall, S.B. & Balda, R.P. (1977) Coadaptations of the Clark’s nutcracker and the piñyon pine for efficient seed harvest and dispersal. Ecological Monographs, 47, 89–111.CrossRefGoogle Scholar
Williams, A., Antonovics, J. & Rolff, J. (2011) Dioecy, hermaphrodites and pathogen load in plants. Oikos, 120, 657–660.CrossRefGoogle Scholar
Yeang, H.-Y. (2007) Synchronous flowering of the rubber tree (Hevea brasiliensis) induced by solar radiation intensity. New Phytologist, 175, 283–289.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org 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
×