Skip to main content

Blephariglottis Group

  • Chapter
  • First Online:

Abstract

Platanthera blephariglottis and P. ciliaris are self-compatible but not autogamous. The positioning of the viscidia and the length of the nectar spur in both species are adapted for attachment of the viscidia to the compound eyes of long-tongued lepidoptera. Distinct pollinator ecotypes may occur in P. ciliaris. In addition to morphological differences, P. chapmanii, P. cristata, and P. integra are separated from one another and other yellow-fringed orchids by pollination biology. P. integrilabia is primarily an outcrossing species, but autogamy can occur. The flowers appear to be adapted to nocturnal sphingids, but only diurnal butterflies have been observed as pollinators. P. clavellata is self-compatible, and both autogamy and outcrossing are reported.

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

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   89.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   119.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
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

Learn about institutional subscriptions

References

  • Beattie A (1978) Plant-animal interactions affecting gene flow in Viola. In: Richards AJ (ed) The pollination of flowers by insects. Dorset Press, Dorchester, Dorset, UK, pp 151–164

    Google Scholar 

  • Brown PM (1998) Checklist of the orchids of North America north of Mexico. N Am Nat Orchid J 4:61–99

    Google Scholar 

  • Brown PM (2002) Resurrection of the genus Gymnadeniopsis Rydb. N Am Nat Orchid J 8:32–40

    Google Scholar 

  • Burd M, Callahan HC (2000) What does the male function hypothesis claim? J Evolutionary Biol 13:735–742

    Article  Google Scholar 

  • Calvo N, Horvitz CC (1990) Pollinator limitation, cost of reproduction, and fitness in plants: a transition matrix demographic approach. Am Nat 136:499–516

    Article  Google Scholar 

  • Case FW Jr (1987) Orchids of the Western Great Lakes Region. Cranbrook Institute of Science, Bloomfield Hills, MI

    Google Scholar 

  • Catling PM (1983) Autogamy in eastern Canadian Orchidaceae: a review of current knowledge and some new observations. Naturaliste Canadien 110:37–54

    Google Scholar 

  • Catling PM (1984) Distribution and pollination biology of Canadian Orchids. In: Tan KN (ed) Proceedings of the 11th world orchid conference, International Press Co., Ltd., Singapore, pp 106–110

    Google Scholar 

  • Catling PM (2011) Notes on the taxonomy, nomenclature, identification, distribution and conservation of the bicolored orchid, Platanthera x bicolor. Native Orchid Conf J 8:11–36

    Google Scholar 

  • Catling PM, Catling VR (1991) A synopsis of breeding systems and pollination in North American orchids. Lindlyana 6:187–210

    Google Scholar 

  • Cole RF, Firmage DH (1984) The floral morphology of Platanthera blephariglottis. Am J Bot 71:700–710

    Article  Google Scholar 

  • Correll DS (1978) Native Orchids of North America North of Mexico, Stanford University Press, Stanford, California

    Google Scholar 

  • Covell CV (1984) A field guide to the moths of Eastern North America. Peterson field guide series (30). Houghton Mifflin Co., Boston, MA

    Google Scholar 

  • Cowden NE (1993) A biosystematic study of Platanthera ciliaris, P. blephariglottis, and P. x biclolor, emphasizing the northern portion of their range. Ph.D. thesis, Miami University, Oxford, OH, USA

    Google Scholar 

  • Cowden NE (1998) Allozyme variability in the Platanthera ciliaris complex. N Am Nat Orchid J 4:241–259

    Google Scholar 

  • Dressler RL (1981) The orchids. Natural history and classification. Harvard University Press, Cambridge, MA

    Google Scholar 

  • Faegri K, van der Pijl L (1971) The principals of pollination ecology, 2nd edn. Pergamon Press, Oxford

    Google Scholar 

  • Firmage DH (1990) The influence of ramet biomass and microhabitat on the reproductive patterns of Platanthera blephariglottis (Orchidaceae). Am J Bot 77:45 (abstract)

    Google Scholar 

  • Firmage DH, Cole FR (1988) Reproductive success and inflorescence size in Calopogon tuberosus (Orchidaceae). Am J Bot 75:1371–1377

    Article  Google Scholar 

  • Folsom JP (1979) The true nature of the putative natural hybrid Platanthera x chapmanii (Orchidaceae). M.S. thesis, Vanderbilt University, Nashville, TN, USA

    Google Scholar 

  • Folsom JP (1984) A reinterpretation of the status and relationships of taxa of the yellow-fringed orchid complex. Orquidea 9:321–346

    Google Scholar 

  • Frame D, Gregg KB (1981) Pollinators of the orchid Platanthera (Habenaria) ciliaris (Linnaeus) Lindley. Assoc Southeast Biol Bull 28:4 (abstract)

    Google Scholar 

  • Frankie GW, Haber WA (1983) Why bees move among mass- flowering neotropical trees. In: Jones CE, Little RJ (eds) Handbook of experimental pollination biology. Van Nostrand Reinhold, New York, pp 360–372

    Google Scholar 

  • Grant V (1977) Organismic evolution. W. H. Freeman & Co., San Francisco

    Google Scholar 

  • Grant V (1983) The systematic and geographical distribution of hawkmoth flowers in the temperate North America flora. Botanical Gazette 144:439–449

    Article  Google Scholar 

  • Gray A (1862) Enumeration of the plants of Dr. Parry’s collection in the Rocky Mountains. Am J Sci Ser 2 34:249–261

    Google Scholar 

  • Gray A (1863) Structure and fertilization of certain orchids. Am J Sci Arts 36:292–294

    Google Scholar 

  • Gregg KB (1981) Reproductive biology of the orchid Platanthera (Habenaria) ciliaris (Linnaeus) Lindley in a wet meadow in West Virginia. Assoc Southeast Biol Bull 28:74 (abstract)

    Google Scholar 

  • Gregg KB (1983) It’s time to watch the orange plumes. W V Native Plant Soc Newsl 2:1–3

    Google Scholar 

  • Gregg KB (1984) Reproductive biology of the orchid Cleistes divaricata (Linnaeus) Ames growing in a West Virginia meadow. Am J Bot 71:79 (abstract)

    Google Scholar 

  • Gregg KB (1990) The natural life cycle of Platanthera In North American Native Terrestrial Orchid Propagation and Production, ed. C. Sawyers, pp. 40–48. Chadds Ford, Pennsylvania: Brandywine Conservancy/Mt. Cuba Center/New England Wildflower Society

    Google Scholar 

  • Hapeman JR, Inoue K (1997) Plant-pollinator interactions and floral radiation in Platanthera (Orchidaceae). In: Givnish TJ, Sytsma KJ (eds) Molecular evolution and adaptive radiation. Cambridge University Press, Cambridge, UK, pp 433–454

    Google Scholar 

  • Hardin JW (1961) A hybrid population of Habenaria and variation in P. blephariglottis. Castanea 26:120–123

    Google Scholar 

  • Heath JE, Adams PA (1967) Regulation of heat production by large moths. J Exp Biol 47:21–33

    PubMed  CAS  Google Scholar 

  • Heinrich B (1976) Flowering phenologies: bog, woodland, and disturbed habitats. Ecology 57:890–899

    Article  Google Scholar 

  • Howe WH (1975) The butterflies of North America. Doubleday, Garden City, NY

    Google Scholar 

  • Judd WW (1958) Studies of the Byron bog in southwestern Ontario. II. The succession and duration of blooming plants. Canad Field-Nat 72:119–121

    Google Scholar 

  • Luer CA (1975) The Native Orchids of the United States and Canada excluding Florida. The New York Botanical Garden, New York

    Google Scholar 

  • Maad J (2000) Phenotypic selection in hawkmoth-pollinated Platanthera bifolia: targets and ­fitness surfaces. Evolution 54:112–123

    PubMed  CAS  Google Scholar 

  • McGrath RT (2008) Contributions to the status and morphology of Platanthera pallida, pale-fringed orchis. N Am Nat Orchid J 14:150–156

    Google Scholar 

  • Montalvo AM, Ackerman JD (1987) Limitations to fruit production in Ionopsis utricularioides (Orchidaceae). Biotropica 19:24–31

    Article  Google Scholar 

  • Morong T (1893) A new species of Listera with notes on other orchids. Bull Torrey Bot Club 20:31–39

    Article  Google Scholar 

  • Nilsson LA (1981) Pollination ecology and evolutionary processes in six species of orchids. Doctoral thesis, Uppsala University, Uppsala, Sweden

    Google Scholar 

  • van der Pijl L, Dodson CH (1966) Orchid flowers, their pollination and evolution. University of Miami Press, Coral Gables, FL

    Google Scholar 

  • Pojar J (1974) Reproductive dynamics of four plant communities of Western British Columbia. Can J Bot 52:1819–1834

    Article  Google Scholar 

  • Reader RJ (1975) Competitive relationships of some bog ericads for major insect pollinators. Can J Bot 53:1300–1305

    Article  Google Scholar 

  • Robertson JL (1987) Pollination and reproductive biology of Platanthera ciliaris in disjunct populations in the Southeastern United States. M.S. thesis, University of Georgia, Athens, Georgia, USA

    Google Scholar 

  • Robertson JL, Wyatt R (1985) Comparative pollination ecology of yellow-fringed orchid in the mountains and coastal plain of the southeastern United States. Am J Bot 72:865 (abstract)

    Google Scholar 

  • Robertson JL, Wyatt R (1990a) Evidence for pollination ecotypes in the yellow-fringed orchid, Platanthera ciliaris. Evolution 44:121–133

    Article  Google Scholar 

  • Robertson JL, Wyatt R (1990b) Reproductive biology of the yellow-fringed orchid, Platanthera ciliaris. Am J Bot 77:388–398

    Article  Google Scholar 

  • Selman CL (1975) A Pictorial Key to the Hawkmoths (Lepidoptera: Sphingidae) of the Eastern United States (except Florida). Ohio State University Press, Columbus, OH

    Google Scholar 

  • Shea MM (1992) Status survey report on Platanthera integrilabia. U.S. Fish and Wildlife Service Agreement No. 14-126-0004-89-956, Work Order No. 90–2

    Google Scholar 

  • Sheviak CJ (2002) Platanthera. In Flora of North America North of Mexico, ed. Flora of North America Editorial Committee, vol 26. Oxford University Press, Oxford, NY, pp 551–571

    Google Scholar 

  • Smith GR (1975) Pollination ecology of Habenaria ciliaris and H. blephariglottis (Orchidaceae). M.A. thesis, Andrews University, Berrien Springs, Michigan, USA

    Google Scholar 

  • Smith GR, Snow GE (1976) Pollination ecology of Platanthera (Habenaria) ciliaris and P. blephariglottis (Orchidaceae). Botanical Gazette 137:133–140

    Article  Google Scholar 

  • Stephenson AG (1979) An evolutionary examination of the floral display of Catalpa speciosa (Bignoniaceae). Evolution 33:1200–1209

    Article  Google Scholar 

  • Stucky IH (1967) Environmental factors and the growth of native orchids. Am J Bot 54:232–241

    Article  Google Scholar 

  • Sutherland S (1986a) Patterns of fruit set: what controls fruit-flower ratios in plants? Evolution 40:117–128

    Article  Google Scholar 

  • Sutherland S (1986b) Floral sex ratios, fruit-set, and resource allocation in plants. Ecology 67:991–1001

    Article  Google Scholar 

  • Sutherland S (1987) Why hermaphroditic plants produce many more flowers than fruits: experimental tests with Agave mckelveyana. Evolution 41:750–759

    Article  Google Scholar 

  • Sutherland S, Delph LF (1984) On the importance of male fitness in plants: patterns of fruit set. Ecology 65:1093–1104

    Article  Google Scholar 

  • Udovic D (1981) Determinants of fruit set in Yucca whipplei: reproductive expenditure vs. ­pollinator availability. Oecologia 48:389–399

    Article  Google Scholar 

  • Zettler LW (1994a) Symbiotic Seed Germination of Platanthera integrilabia (Correll) Luer, an Endangered Terrestrial Orchid. Ph.D. dissertation, Clemson University, Clemson, South Carolina

    Google Scholar 

  • Zettler LW (1994b) Extinction in our own backyard. Am Orchid Soc Bull 63:686–688

    Google Scholar 

  • Zettler LW, Ahuja NS, McInnis TS Jr (1996) Insect pollination of the endangered monkey-face orchid (Platanthera integrilabia) in McMinn County, Tennessee: One last glimpse of a once common spectacle. Castanea 61:14–24

    Google Scholar 

  • Zettler LW, Fairey JE III (1990) The status of Platanthera integrilabia (Correll) Luer, an endangered terrestrial orchid. Lindleyana 5:212–217

    Google Scholar 

  • Zettler LW, McInnis TM Jr (1992) Propagation of Platanthera integrilabia (Correll) Luer, an endangered terrestrial orchid, through symbiotic seed germination. Lindlyana 7:154–161

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Charles L. Argue Ph.D. .

Rights and permissions

Reprints and permissions

Copyright information

© 2012 Springer Science+Business Media, LLC

About this chapter

Cite this chapter

Argue, C.L. (2012). Blephariglottis Group. In: The Pollination Biology of North American Orchids: Volume 1. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-0592-4_12

Download citation

Publish with us

Policies and ethics