Floral biology of Eriope blanchetii (Lamiaceae) in coastal sand dunes of NE Brazil

The floral biology of the sand dune shrub Eriope blanchetii (Benth) Harley was investigated in a wild population located within an environment protection area near Salvador, NE Brazil. Inflorescence and flower development were monitored, and the reproductive biology was assessed. Inflorescences are...

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Published inAustral ecology Vol. 30; no. 3; pp. 243 - 249
Main Authors DA SILVA, FABIANA O., VIANA, BLANDINA F., JACOBI, CLAUDIA M.
Format Journal Article
LanguageEnglish
Published Melbourne, Australia Blackwell Science Pty 01.05.2005
Blackwell
Blackwell Publishing Ltd
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Abstract The floral biology of the sand dune shrub Eriope blanchetii (Benth) Harley was investigated in a wild population located within an environment protection area near Salvador, NE Brazil. Inflorescence and flower development were monitored, and the reproductive biology was assessed. Inflorescences are terminal panicles, each bearing from one to 38 small, zygomorphic flowers. The duration of an inflorescence is about 2 months, with few new flowers each day. The rewards to visitors are pollen and nectar, the latter being produced in small quantities at the corolla base, near the stylopodium. Three sequential phases of flower development were identified, based on colour changes, pollen and nectar availability, and stigmatic receptivity. Anthesis takes place throughout the day within each plant, and flowers are strongly protandrous. Flowers are short‐lived, with individual variations of 7–30 h until corolla abscission. This variation is probably associated to a post‐pollinating response, which reduces the length of the female phase and could be advantageous for the economy of nectar production and for increased efficient pollination of the remaining flowers on a plant. The results of the pollination tests (apomixis, spontaneous and manual autogamy, manual cross‐pollination, and control) reinforced the role of pollinators for the reproductive success of E. blanchetii, given that the production of fruits from spontaneous pollination is unlikely to be resulting from protandry and given the morphological floral features. Taken together, the morphological and physiological aspects of E. blanchetii floral biology favour cross‐pollination, and it is likely that most of the fruits in nature are produced by outcrossing.
AbstractList Abstract  The floral biology of the sand dune shrub Eriope blanchetii (Benth) Harley was investigated in a wild population located within an environment protection area near Salvador, NE Brazil. Inflorescence and flower development were monitored, and the reproductive biology was assessed. Inflorescences are terminal panicles, each bearing from one to 38 small, zygomorphic flowers. The duration of an inflorescence is about 2 months, with few new flowers each day. The rewards to visitors are pollen and nectar, the latter being produced in small quantities at the corolla base, near the stylopodium. Three sequential phases of flower development were identified, based on colour changes, pollen and nectar availability, and stigmatic receptivity. Anthesis takes place throughout the day within each plant, and flowers are strongly protandrous. Flowers are short‐lived, with individual variations of 7–30 h until corolla abscission. This variation is probably associated to a post‐pollinating response, which reduces the length of the female phase and could be advantageous for the economy of nectar production and for increased efficient pollination of the remaining flowers on a plant. The results of the pollination tests (apomixis, spontaneous and manual autogamy, manual cross‐pollination, and control) reinforced the role of pollinators for the reproductive success of E. blanchetii , given that the production of fruits from spontaneous pollination is unlikely to be resulting from protandry and given the morphological floral features. Taken together, the morphological and physiological aspects of E. blanchetii floral biology favour cross‐pollination, and it is likely that most of the fruits in nature are produced by outcrossing.
The floral biology of the sand dune shrub Eriope blanchetii (Benth) Harley was investigated in a wild population located within an environment protection area near Salvador, NE Brazil. Inflorescence and flower development were monitored, and the reproductive biology was assessed. Inflorescences are terminal panicles, each bearing from one to 38 small, zygomorphic flowers. The duration of an inflorescence is about 2 months, with few new flowers each day. The rewards to visitors are pollen and nectar, the latter being produced in small quantities at the corolla base, near the stylopodium. Three sequential phases of flower development were identified, based on colour changes, pollen and nectar availability, and stigmatic receptivity. Anthesis takes place throughout the day within each plant, and flowers are strongly protandrous. Flowers are short‐lived, with individual variations of 7–30 h until corolla abscission. This variation is probably associated to a post‐pollinating response, which reduces the length of the female phase and could be advantageous for the economy of nectar production and for increased efficient pollination of the remaining flowers on a plant. The results of the pollination tests (apomixis, spontaneous and manual autogamy, manual cross‐pollination, and control) reinforced the role of pollinators for the reproductive success of E. blanchetii, given that the production of fruits from spontaneous pollination is unlikely to be resulting from protandry and given the morphological floral features. Taken together, the morphological and physiological aspects of E. blanchetii floral biology favour cross‐pollination, and it is likely that most of the fruits in nature are produced by outcrossing.
The floral biology of the sand dune shrub Eriope blanchetii (Benth) Harley was investigated in a wild population located within an environment protection area near Salvador, NE Brazil. Inflorescence and flower development were monitored, and the reproductive biology was assessed. Inflorescences are terminal panicles, each bearing from one to 38 small, zygomorphic flowers. The duration of an inflorescence is about 2 months, with few new flowers each day. The rewards to visitors are pollen and nectar, the latter being produced in small quantities at the corolla base, near the stylopodium. Three sequential phases of flower development were identified, based on colour changes, pollen and nectar availability, and stigmatic receptivity. Anthesis takes place throughout the day within each plant, and flowers are strongly protandrous. Flowers are short-lived, with individual variations of 7-30 h until corolla abscission. This variation is probably associated to a post-pollinating response, which reduces the length of the female phase and could be advantageous for the economy of nectar production and for increased efficient pollination of the remaining flowers on a plant. The results of the pollination tests (apomixis, spontaneous and manual autogamy, manual cross-pollination, and control) reinforced the role of pollinators for the reproductive success of E. blanchetii, given that the production of fruits from spontaneous pollination is unlikely to be resulting from protandry and given the morphological floral features. Taken together, the morphological and physiological aspects of E. blanchetii floral biology favour cross-pollination, and it is likely that most of the fruits in nature are produced by outcrossing. [PUBLICATION ABSTRACT]
Author JACOBI, CLAUDIA M.
DA SILVA, FABIANA O.
VIANA, BLANDINA F.
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Issue 3
Keywords Flower
Sand
anthesis
resources production
'restinga' vegetation
floral morphology
sand dune
Floral biology
reproductive strategy
Labiatae
Dicotyledones
Morphology
Angiospermae
Vegetation
Flowering
Strategy
Spermatophyta
Coastal dune
Language English
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References_xml – reference: Herrera C. M. (1987) Componentes del flujo génico en Lavandula latifolia Medicus: polinización y dispersión de semillas. An. Jard. Bot. Madrid 44, 49-61.
– reference: Kearns C. A., Inouye D. W. & Waser N. M. (1998) Endangered mutualisms: the conservation of plant-pollinator interactions. Annu. Rev. Ecol. Syst. 29, 83-112.
– reference: Stannard B. L., Harvey Y. B. & Harley R. M. (1995) Flora of the Pico das Almas: Chapada Diamantina, Bahia, Brasil. Royal Botanic Gardens Kew, London.
– reference: Dafni A. (1992) Pollination Ecology: a Practical Approach. Oxford University Press Inc., New York.
– reference: Zar J. H. (1984) Biostatistical Analysis, 2nd edn. Prentice Hall International Inc., London.
– reference: Wcislo W. T. & Cane J. H. (1996) Floral resource utilization by solitary bees (Hymenoptera: Apoidea) and Explotation of their stored foods by natural enemies. Annu. Rev. Entomol. 41, 257-86.
– reference: Endress P. K. (1994) Diversity and Evolutionary Biology of Tropical Flowers. Cambridge University Press, Cambridge.
– reference: Araujo D. S. D. & Lacerda L. D. (1987) A natureza das restingas. Ciência Hoje 33, 42-8.
– reference: Harley R. M. (1971) An explosive pollination mechanism in Eriope crassipes, a Brazilian labiate. Bot. J. Linn. Soc. 3, 159-64.
– reference: Britto I. C., QueiroZ. L. P., Guedes M. L. S., Oliveira N. C. & Silva L. B. (1993) Flora fanerogâmica das dunas e lagoas de Abaeté, Salvador, Bahia. Sitientibus 11, 31-46.
– reference: Westerkamp C. (1996) Pollen in bee-flower relations: some considerations on melittophily. Bot. Acta 109, 325-32.
– reference: Silva F. O. & Viana B. F. (2002) Os visitantes florais de. Eriope Blanchetii (Benth) Harley (Lamiaceae) nas dunas costeiras de Abaeté, Salvador, Bahia. Sitientibus. 2, 3-10.
– reference: Rudall P. (1981) Flower anatomy of the subtribe Hyptidinae (Labiatae). Bot. J. Linn. Soc. 8, 251-62.
– reference: Whitten W. M. (1981) Pollination ecology of Monarda didyma, M. clinopodia, and hybrids (Lamiaceae) in the Southern Appalachian Mountains. Am. J. Bot. 68, 435-42.
– reference: Remold S. & Meyrat A. (1991) El efecto de la polinización en la hora de abscisión de la corola de Crescentia alata. Agroecologia Neotropical 1, 22-6.
– reference: Harley R. M. (1976) Hooker's Icones Plantarum: A Review of Eriope and Eriopdion (Labiatae). Royal Botanic Gardens Kew, London.
– reference: Cruden R. W., HermanutZ. L. & Shuttleworth J. (1984) The pollination biology and breeding system of Monarda fistulosa (Labiatae). Oecologia 64, 104-10.
– reference: Kearns C. A. & Inouye D. W. (1993) Techniques for Pollination Biologists.Colorado University Press, Niewot, Colorado.
– reference: Costa J. A. S. & Ramalho M. (2001) Ecologia da polinização em ambiente de duna tropical (APA do Abaeté, Salvador, Bahia, Brasil). Sitientibus 1, 141-53.
– reference: Faegri K. & Van Der Pijl L. (1979) The Principles of Pollination Ecology, 3rd edn. Pergamon Press, Oxford.
– reference: Heirich B. (1975) Bee flowers: a hypothesis on flower variety and blooming times. Evolution. 29, 325-34.
– volume: 1
  start-page: 141
  year: 2001
  end-page: 53
  article-title: Ecologia da polinização em ambiente de duna tropical (APA do Abaeté, Salvador, Bahia, Brasil)
  publication-title: Sitientibus
– volume: 68
  start-page: 435
  year: 1981
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Snippet The floral biology of the sand dune shrub Eriope blanchetii (Benth) Harley was investigated in a wild population located within an environment protection area...
Abstract  The floral biology of the sand dune shrub Eriope blanchetii (Benth) Harley was investigated in a wild population located within an environment...
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SubjectTerms 'restinga' vegetation
Abscission
Animal and plant ecology
Animal, plant and microbial ecology
anthesis
Biological and medical sciences
Biology
Botany
Brazil
coastal dune soils
Coasts
Cross-pollination
Dunes
Environmental protection
floral morphology
flowering
Flowers
Fruits
Fundamental and applied biological sciences. Psychology
General aspects
inflorescences
insect pollination
Lamiaceae
Pollen
pollinating insects
Pollination
Pollinators
Reproduction
reproductive strategy
resources production
Sand
Sand & gravel
sand dune
Self-fertilization
Title Floral biology of Eriope blanchetii (Lamiaceae) in coastal sand dunes of NE Brazil
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Volume 30
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