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 in | Austral ecology Vol. 30; no. 3; pp. 243 - 249 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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. |
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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. |
Author_xml | – sequence: 1 givenname: FABIANA O. surname: DA SILVA fullname: DA SILVA, FABIANA O. organization: Faculdade Tecnologia e Ciências (FTC), Salvador, e Faculdades Jorge Amado (FJA), Paralela – sequence: 2 givenname: BLANDINA F. surname: VIANA fullname: VIANA, BLANDINA F. organization: Universidade Federal da Bahia, Instituto de Biologia, Departamento de Zoologia, Laboratório de Biologia e Ecologia de Abelhas (LABEA), Rua Barão de Geremoabo s/n, Campus Universitário de Ondina, 40.170.110, Salvador, BA, Brazil (Email: blandefv@ufba.br) and – sequence: 3 givenname: CLAUDIA M. surname: JACOBI fullname: JACOBI, CLAUDIA M. organization: Universidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Departamento de Biologia Geral, Belo Horizonte, Minas Gerais, Brazil |
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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 |
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References | Cruden R. W., HermanutZ. L. & Shuttleworth J. (1984) The pollination biology and breeding system of Monarda fistulosa (Labiatae). Oecologia 64, 104-10. Zar J. H. (1984) Biostatistical Analysis, 2nd edn. Prentice Hall International Inc., London. Harley R. M. (1976) Hooker's Icones Plantarum: A Review of Eriope and Eriopdion (Labiatae). Royal Botanic Gardens Kew, London. 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. Kearns C. A. & Inouye D. W. (1993) Techniques for Pollination Biologists.Colorado University Press, Niewot, Colorado. 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. 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. Westerkamp C. (1996) Pollen in bee-flower relations: some considerations on melittophily. Bot. Acta 109, 325-32. 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. Endress P. K. (1994) Diversity and Evolutionary Biology of Tropical Flowers. Cambridge University Press, Cambridge. Heirich B. (1975) Bee flowers: a hypothesis on flower variety and blooming times. Evolution. 29, 325-34. 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. Harley R. M. (1971) An explosive pollination mechanism in Eriope crassipes, a Brazilian labiate. Bot. J. Linn. Soc. 3, 159-64. 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. Dafni A. (1992) Pollination Ecology: a Practical Approach. Oxford University Press Inc., New York. 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. Faegri K. & Van Der Pijl L. (1979) The Principles of Pollination Ecology, 3rd edn. Pergamon Press, Oxford. 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. Herrera C. M. (1987) Componentes del flujo génico en Lavandula latifolia Medicus: polinización y dispersión de semillas. An. Jard. Bot. Madrid 44, 49-61. Rudall P. (1981) Flower anatomy of the subtribe Hyptidinae (Labiatae). Bot. J. Linn. Soc. 8, 251-62. Araujo D. S. D. & Lacerda L. D. (1987) A natureza das restingas. Ciência Hoje 33, 42-8. 1987; 33 1998; 29 1984; 64 1991; 1 1996; 109 1998 1976 2002; 2 1981; 68 1981; 8 1995 1994 1993 1992 1979 1999 1987; 44 1993; 11 1975; 29 1996; 41 1984 2001; 1 1983; Vol. VII 1988 1971; 3 Araujo D. S. D. (e_1_2_6_3_1) 1984 Faegri K. (e_1_2_6_10_1) 1979 Huck R. (e_1_2_6_16_1) 1992 Stannard B. L. (e_1_2_6_26_1) 1995 e_1_2_6_30_1 Harley R. M. (e_1_2_6_13_1) 1976 Zar J. H. (e_1_2_6_31_1) 1984 Silva F. O. (e_1_2_6_25_1) 2002; 2 Costa J. A. S. (e_1_2_6_6_1) 2001; 1 e_1_2_6_19_1 Giulietti A. M. (e_1_2_6_11_1) 1988 e_1_2_6_12_1 e_1_2_6_18_1 Pinto G. L. P. (e_1_2_6_21_1) 1984 Remold S. (e_1_2_6_22_1) 1991; 1 Araujo D. S. D. (e_1_2_6_4_1) 1987; 33 Britto I. C. (e_1_2_6_5_1) 1993; 11 Morawetz W. (e_1_2_6_20_1) 1983 Dafni A. (e_1_2_6_8_1) 1992 Herrera C. M. (e_1_2_6_15_1) 1987; 44 e_1_2_6_7_1 Heirich B. (e_1_2_6_14_1) 1975; 29 e_1_2_6_24_1 e_1_2_6_23_1 e_1_2_6_2_1 Endress P. K. (e_1_2_6_9_1) 1994 Kearns C. A. (e_1_2_6_17_1) 1993 e_1_2_6_29_1 e_1_2_6_28_1 e_1_2_6_27_1 |
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 end-page: 42 article-title: Pollination ecology of , , and hybrids (Lamiaceae) in the Southern Appalachian Mountains publication-title: Am. J. Bot. – volume: 2 start-page: 3 year: 2002 end-page: 10 article-title: Os visitantes florais de. (Benth) Harley (Lamiaceae) nas dunas costeiras de Abaeté, Salvador, Bahia publication-title: Sitientibus. – volume: 64 start-page: 104 year: 1984 end-page: 10 article-title: The pollination biology and breeding system of (Labiatae) publication-title: Oecologia – volume: 29 start-page: 83 year: 1998 end-page: 112 article-title: Endangered mutualisms: the conservation of plant–pollinator interactions publication-title: Annu. Rev. Ecol. Syst. – volume: 44 start-page: 49 year: 1987 end-page: 61 article-title: Componentes del flujo génico en Medicus: polinización y dispersión de semillas publication-title: An. Jard. Bot. Madrid – volume: 33 start-page: 42 year: 1987 end-page: 8 article-title: A natureza das restingas publication-title: Ciência Hoje – volume: 3 start-page: 159 year: 1971 end-page: 64 article-title: An explosive pollination mechanism in , a Brazilian labiate publication-title: Bot. J. Linn. 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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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