Plant Ecology

, Volume 193, Issue 1, pp 59–69 | Cite as

Pollination biology of a disjunct population of the endangered sandhills endemic Penstemon haydenii S. Wats. (Scrophulariaceae) in Wyoming, USA

  • Vincent J. Tepedino
  • Trent R. Toler
  • Brosi A. Bradley
  • Jessica L. Hawk
  • Terry L. Griswold
Original Paper

Abstract

We studied the breeding system and flower visitors of the endangered plant, Penstemon haydenii, at several south-central Wyoming, USA occurrences. In agreement with earlier studies of the species 300 km to the east in Nebraska, we found Wyoming plants to be self-incompatible and pollinator-dependent for sexual reproduction. Flower visitors were several species of native bees in the families Apidae (particularly bumblebees), Halictidae (small sweat bees), and Megachilidae (especially in the genus Osmia); and the masarid wasp Pseudomasaris vespoides. Especially important was Osmia brevis, an abundant megachilid bee, and one of only two species (the sweat bee Lasioglossum (Dialictus) pruinosum was the other) present at all five sites. As in Nebraska, fruit set did not differ between our experimental cross-pollination treatment and an open-pollinated control. However, unlike Nebraska, open-pollinated treatments in Wyoming produced significantly fewer seeds per fruit than the experimental out-crossing treatment. We discuss several possible explanations for seed limitation: (1) a scarcity of pollinators early in the flowering season; (2) resource competition for developing ovules on open-pollinated inflorescences but not on experimental inflorescences; (3) the deposition of self pollen through intra-inflorescence and intra-genet pollinator movements; (4) few S-alleles and mating types in the Wyoming metapopulation compared to the Nebraska metapopulation, from which it likely derives.

Keywords

Breeding system Reproductive limitation Bees Pollinators Beardtongue Rare Conservation 

Notes

Acknowledgements

Funding was supplied by USDI-Bureau of Land Management in Rawlins WY. We especially thank Frank Blomquist of that office for discovering the plant in Wyoming in 1996, for initiating the study that made this project possible, and for providing support throughout. Bonnie Heidel, Wyoming Natural Diversity Database, Univ. of Wyoming, Laramie, was also instrumental in facilitating this research. Alice Bain helped with the fieldwork.

References

  1. Ahlbrandt TS, Swinehart JB, Maroney DG (1983) The dynamic Holocene dune fields of the Great Plains and Rocky Mountain Basins, USA. In: Brookfield ME, Ahlbrandt TS (eds) Developments on sedimentology, vol 38, Eolian sediments and processes. Elsevier, New York, pp 379–406Google Scholar
  2. Aigner PA (2004) Ecological and genetic effects on demographic processes: pollination, clonality and seed production in Dithyrea maritima. Biol Conserv 116:27–34CrossRefGoogle Scholar
  3. Aizen MA, Ashworth L, Galetto L (2002) Reproductive success in fragmented habitats: do compatibility systems and pollination specialization matter? J Veg Sci 13:885–892CrossRefGoogle Scholar
  4. Baker HG (1955) Self-compatibility and establishment after “long-distance” dispersal. Evolution 9:347–348CrossRefGoogle Scholar
  5. Barrett SCH, Eckert CG (1990) Variation and evolution of mating systems in seed plants. In: Kawano S (ed), Biological approaches and evolutionary trends in plants. Academic Press, New York, pp 229–254Google Scholar
  6. Beattie AJ (1971) A technique for the study of insect-borne pollen. Pan-Pac Entomol 47:82Google Scholar
  7. Burd M (1994) Bateman’s principle and plant reproduction: the role of pollen limitation in fruit and seed set. Bot Rev 60:83–139Google Scholar
  8. Busch JW (2005) The evolution of self-compatibility in geographically peripheral populations of Leavenworthia alabamica (Brassicaceae). Am J Bot 92:1503–1512Google Scholar
  9. Caha CA, Lee DJ, Stubbendieck J (1998) Organellar genetic diversity in Penstemon haydenii (Scrophulariaceae): an endangered plant species. Am J Bot 85:1704–1709CrossRefGoogle Scholar
  10. Cooper KW (1952) Records and flower preferences of masarid wasps. II. Polytrophy or oligotrophy in Pseudomasaris? Am Midl Nat 48:103–110CrossRefGoogle Scholar
  11. Crosswhite FS, Crosswhite CD (1966) Insect pollinators of Penstemon Series Graciles (Scrophulariaceae) with notes on Osmia and other Megachilidae. Am Midl Nat 76:450–467CrossRefGoogle Scholar
  12. DeMauro MM (1993) Relationship of breeding system to rarity in the lakeside daisy (Hymenoxys acaulis var. glabra). Conserv Biol 7:542–550CrossRefGoogle Scholar
  13. Fertig W (2001) 2000 survey for Blowout Penstemon (Penstemon haydenii) in Wyoming. US Department of the Interior, Bureau of Land Management, Cheyenne WY 40 pp. http://uwadmnweb.uwyo.edu/WYNDD/Reports/pdf_fertig/Fertig_01_Penstemon_haydenii.pdfGoogle Scholar
  14. Flessner TR, Stubbendieck J (1989) Propagation of Blowout Penstemon (Penstemon haydenii S. Watson). In: Bragg TB, Stubbendieck J (eds) Proceedings of the 11th North American Prairie conference, Lincoln, NE, pp 237–239Google Scholar
  15. Flessner TR, Stubbendieck J (1992) Pollination characteristics of Blowout Penstemon (Penstemon haydenii S. Watson). Trans Nebr Acad Sci 19:63–66Google Scholar
  16. Freeman CC (1981) A biosystematic study of the genus Penstemon (Scrophulariaceae) in the Great Plains. MS Thesis, Kansas State University, Manhattan, KSGoogle Scholar
  17. Freeman CC (1986) Penstemon. In: Flora of the great plains. Great Plains Assoc., University Press of Kansas, Lawrence, KS, pp 774–789Google Scholar
  18. Fritz M, Stubbendieck J, Jobman W (1992) Blowout penstemon (Penstemon haydenii S. Wats.) recovery plan. US Fish and Wildlife Service, Denver, CO. http://ecos.fws.gov/docs/recovery_plans/1992/920717.pdfGoogle Scholar
  19. Hawk JL, Tepedino VJ (in press) The effect of staminode removal on female reproductive success in a Wyoming population of the endangered Blowout penstemon, Penstemon haydenii S. Wats. (Scrophulariaceae). Madroño 54Google Scholar
  20. Heidel B (2005) Survey of Penstemon haydenii (Blowout Penstemon) in Wyoming 2004. US Department of the Interior, Bureau of Land Management, Rawlins-Casper, WY. http://uwadmnweb.uwyo.edu/wyndd/Reports/reports_heidel.htmGoogle Scholar
  21. Herlihy CR, Eckert CG (2005) Evolution of self-fertilization at geographical range margins? A comparison of demographic, floral, and mating system variables in central vs. peripheral populations of Aquilegia canadensis (Ranunculaceae). Am J Bot 92:744–751Google Scholar
  22. Herrera CM (1996) Floral traits and plant adaptation to insect pollinators: a devil’s advocate approach. In: Lloyd DG, Barrett SCH (eds), Floral biology. Chapman & Hall, New York, pp 65–87Google Scholar
  23. Husband B, Barrett SCH (1996) A metapopulation perspective in plant population biology. J Ecol 84:461–469CrossRefGoogle Scholar
  24. Jain SK (1976) The evolution of inbreeding in plants. Annu Rev Ecol Syst 7:469–495CrossRefGoogle Scholar
  25. Karron JD (1991) Patterns of genetic variation and breeding systems in rare plant species. In: Falk DA, Holsinger KE (eds) Genetics and conservation of rare plants. Oxford University Press, New York, pp 87–98Google Scholar
  26. Lawson HR, Tepedino VJ, Griswold TL (1989) Pollen collectors and other insect visitors to Penstemon haydenii S. Wats. In: Bragg TB, Stubbendieck J (eds) Proceedings of the 11th North American Prairie conference, Lincoln, NE, pp 233–235Google Scholar
  27. Lee TD (1988) Patterns of fruit and seed production. In: Lovett Doust J, Lovett Doust L (eds) Plant reproductive ecology: patterns and strategies. Oxford University Press, New York, pp 179–202Google Scholar
  28. Lesica P, Yurkewycz R, Crone EE (2006) Rare plants are common where you find them. Am J Bot 93:454–459Google Scholar
  29. Levin DA (1972a) Low frequency disadvantage in the exploitation of pollinators by corolla variants in Phlox. Am Nat 106:453–460CrossRefGoogle Scholar
  30. Levin DA (1972b) Competition for pollinator service: a stimulus for the evolution of autogamy. Evolution 26:668–674CrossRefGoogle Scholar
  31. Mayer JH, Mahan SA (2004) Late quaternary stratigraphy and geochronology of the western Killpecker Dunes, Wyoming, USA. Quaternary Res 61:72–84CrossRefGoogle Scholar
  32. Michener CD (2000) The bees of the world. Johns Hopkins Univ Press, Baltimore, MDGoogle Scholar
  33. Moeller DA, Geber MA (2005) Ecological context of the evolution of self-pollination in Clarkia xantiana: population size, plant communities, and reproductive assurance. Evolution 59:786–799PubMedGoogle Scholar
  34. Muhs DR, Stafford Jr TW, Swinehart JB, Cowherd SD, Mahan SA, Bush CA, Madole RF, Maat PB (1997) Late Holocene eolian activity in the mineralogically mature Nebraska sand hills. Quaternary Res 48:162–176CrossRefGoogle Scholar
  35. Nold R (1999) Penstemons. Timber Press, Portland, ORGoogle Scholar
  36. Price MV, Waser NM, Irwin RE, Campbell DR, Brody AK (2005) Temporal and spatial variation in pollination of a montane herb: a seven-year study. Ecology 86:2106–2116CrossRefGoogle Scholar
  37. Robertson JL, Wyatt R (1990) Evidence for pollination ecotypes in the yellow-fringed orchid, Platanthera ciliaris. Evolution 44:121–133CrossRefGoogle Scholar
  38. Sánchez-LaFuente AM (2002) Floral variation in the generalist perennial herb Paeonia broteroi (Paeoniaceae): differences between regions with different pollinators and herbivores. Am J Bot 89:1260–1269Google Scholar
  39. Simpson BB, Neff JL (1987) Pollination ecology in the arid southwest. Aliso 11:417–440Google Scholar
  40. Stebbins GL (1970) Adaptive radiation of reproductive characteristics in Angiosperms, I: Pollination mechanisms. Annu Rev Ecol Syst 1:307–326CrossRefGoogle Scholar
  41. Stokes S, Gaylord DR (1993) Optical dating of Holocene dune sands in the Ferris dune field. Quaternary Res 39:274–281CrossRefGoogle Scholar
  42. Stone JL, Sasuclark MA, Blomberg CP (2006) Variation in the self-compatibility response within and among populations of the tropical shrub Witheringia solanacea (Solanaceae). Am J Bot 93:592–598Google Scholar
  43. Straw RM (1956) Adaptive morphology of the Penstemon flower. Phytomorphology 6:112–119Google Scholar
  44. Tepedino VJ (1979) The importance of bees and other insect pollinators in maintaining floral species composition. In: The endangered species: a symposium. Great Basin Nat Memoirs 3:139–150Google Scholar
  45. Tepedino VJ, Sipes SD, Griswold TL (1999) The reproductive biology and effective pollinators of the endangered beardtongue Penstemon penlandii (Scrophulariaceae). Plant Syst Evol 219:39–54CrossRefGoogle Scholar
  46. Tepedino VJ, Bowlin WR, Griswold TL (in press) The pollination biology of the endangered Blowout Penstemon (Penstemon haydenii S. Wats.: Scrophulariaceae) in Nebraska. J Torrey Bot Soc 134Google Scholar
  47. Torchio PF (1974) Mechanisms involved in the pollination of Penstemon visited by the masarid wasp, Pseudomasaris vespoides (Cresson). Pan-Pac Entomol 50:226–234Google Scholar
  48. Weller SG (1994) The relationship of rarity to plant reproductive biology. In: Bowles ML, Whelan CJ (eds) Restoration of endangered species: conceptual issues, planning and implementation. Cambridge University Press, New York, pp 90–117Google Scholar
  49. Zimmerman M, Pyke GH (1988) Reproduction in Polemonium: assessing factors limiting seed set. Am Nat 131:723–738CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, Inc. 2006

Authors and Affiliations

  • Vincent J. Tepedino
    • 1
  • Trent R. Toler
    • 2
  • Brosi A. Bradley
    • 3
  • Jessica L. Hawk
    • 4
  • Terry L. Griswold
    • 1
  1. 1.USDA ARS Bee Biology & Systematics Lab, Department of BiologyUtah State UniversityLoganUSA
  2. 2.Department of BiologyUtah State UniversityLoganUSA
  3. 3.Juniata CollegeHuntingdonUSA
  4. 4.New OrleansUSA

Personalised recommendations