Skip to main content

The Structure of Pollen

  • Chapter
  • First Online:
Pollen Allergy in a Changing World
  • 112 Accesses

Abstract

In plants, the life cycle is an alternation between a diploid, spore-producing multicellular generation (the sporophyte) and a haploid, also multicellular generation (the gametophyte), producing sperm and/or egg cells [1, 2]. Pollen is a biological structure functioning as a container, in which is housed male gametophyte generation of the angiosperms and gymnosperms. Such a container is an evolutionary adaptation for life out of water because it protects male gametes from adverse atmospheric influence while transferring from anthers to pistils. Each pollen grain contains vegetative (nonreproductive) cells and a generative (reproductive) cell. In flowering plants, the vegetative tube cell produces the pollen tube, and the generative cell divides to form the two sperm cells. A pollen grain contains the male gametophyte of the seed plant, i.e. the sperm-producing generation (gymnosperms and angiosperms). In seedless plants, gametophytes are generally independent from the sporophyte and consist of hundreds of cells; evolution of the seed-bearing habit involved dependence of the gametophytes upon sporophytes and reduction of their size. Thus, in gymnosperms, the male gametophyte has up to ten cells, whereas in angiosperms, there is only one vegetative cell apart from the two sperm cells. Each grain has an internal limiting cellulose membrane, the intine, and a two-layered external covering, the exine, composed of a durable substance called sporopollenin which is primarily a high molecular weight polymer of fatty acids. The male gametophyte originates from a spore, generally called a microspore, and is still surrounded by this spore’s sporopollenin outer wall, the exine, at maturity. The gametophyte’s own wall is called the intine.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Moore PD, Webb JA. An illustrated guide to pollen analysis. London: Hodder and Stoughton; 1983. p. 133.

    Google Scholar 

  2. Johnstone A. Biology: facts & practice for a level. Oxford: Oxford University Press; 2001. p. 95.

    Google Scholar 

  3. Pleasants JM, Hellmich RL, Dively GP, Sears MK, Stanley-Horn DE, Mattila HR, Foster JE, Clark P, Jones GD. Corn pollen deposition on milkweeds in and near cornfields. Proc Natl Acad Sci U S A. 2001;98(21):11919–24.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Furness CA, Rudall PJ. Pollen and anther characters in monocot systematics. Grana. 2001;40:17–25.

    Article  Google Scholar 

  5. Lewis WR, Vinay P, Zenger VE. Airborne and allergenic pollen of North America. Baltimore: The Johns Hopkins University Press; 1983.

    Google Scholar 

  6. Weber RW, Nelson HS. Pollen allergens and their interrelationships. Clin Rev Allergy. 1985;3:291–318.

    Article  CAS  PubMed  Google Scholar 

  7. Smith EG. Sampling and identifying allergenic pollens and molds. San Antonio: Bluestone; 1984. p. 1984.

    Google Scholar 

  8. Alan RH, Imogen P. The evolution of plant physiology. London: Elsevier Academic Press; 2004. p. 45.

    Google Scholar 

  9. Furness CA, Rudall PJ. Pollen aperture evolution: a crucial factor for eudicot success? Trends Plant Sci. 2004;9(3):154–8.

    Article  CAS  PubMed  Google Scholar 

  10. Furness CA, Rudall PJ. Apertures with lids: distribution and significance of operculate pollen in monocotyledons. Int J Plant Sci. 2003;164:835–54.

    Article  Google Scholar 

  11. Sporne KR. Some observations on the evolution of pollen types in dicotyledons. New Phytol. 1972;71:181–5.

    Article  Google Scholar 

  12. Simpson MG. Palynology. Plant systematics. New York: Academic; 2011. p. 453–64.

    Google Scholar 

  13. Singh G. Palynology. Plant systematics: an integrated approach. New Delhi: Science Publishers; 2004. p. 142.

    Google Scholar 

  14. Judd WS, Olmstead RG. A survey of tricolpate (eudicot) phylogenetic relationships. Am J Bot. 2004;91:1627–44.

    Article  PubMed  Google Scholar 

  15. Skvarla JJ, Raven PH, Praglowski J. The evolution of pollen tetrads in Onagraceae. Am J Bot. 1975;62:6.

    Article  PubMed  Google Scholar 

  16. Ngo AH, Kanehara K, Nakamura Y. Non-specific phospholipases C, NPC2 and NPC6, are required for root growth in Arabidopsis. Plant J. 2019;100:825–35.

    Article  CAS  PubMed  Google Scholar 

  17. Ngo AH, Lin YC, Liu YC, Gutbrod K, Peisker H, Dörmann P, et al. A pair of nonspecific phospholipases C, NPC2 and NPC6, are involved in gametophyte development and glycerolipid metabolism in Arabidopsis. New Phytol. 2018;219:163–75.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jae-Won Oh .

Rights and permissions

Reprints and permissions

Copyright information

© 2023 The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd.

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Oh, JW. (2023). The Structure of Pollen. In: Pollen Allergy in a Changing World . Springer, Singapore. https://doi.org/10.1007/978-981-99-4645-7_4

Download citation

  • DOI: https://doi.org/10.1007/978-981-99-4645-7_4

  • Published:

  • Publisher Name: Springer, Singapore

  • Print ISBN: 978-981-99-4644-0

  • Online ISBN: 978-981-99-4645-7

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics