4.3 Article

Flower scent composition in night-flowering Silene species (Caryophyllaceae)

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BIOCHEMICAL SYSTEMATICS AND ECOLOGY
卷 30, 期 5, 页码 383-397

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0305-1978(01)00106-5

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caryophyllaceae; Silene; flower scent; nocturnal pollination; headspace adsorption

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Floral scent of 13 night-flowering Silene species (Caryophyllaceae) was collected by head-space adsorption and analysed via gas chromatography and mass spectrometry. Benzenoids together with isoprenoids dominated the scent in all species. Among the benzenoids, benzaldehyde (Silene subconica 35.5%, Silene succulenta 23.1%, Silene sericea 15.6%, Silene vulgaris 12.2%, and Silene nutans 9.9%), methylbenzoate (Silene saxifraga 96.1%, S. succulenta 15.2%), benzyl acetate (Silene dichotoma 37.8%, S. nutans 30.1%, Silene italica 9.0%, and Silene latifolia 5.5%), or benzyl alcohol (Silene viscosa 36.1%) occur in the largest amounts. p-Cresol is only found in the floral scent of S. dichotoma (28.5%). Among the isoprenoids, monoterpenes occur in the largest amounts (myrcene 23% in Silene chlorantha, trans-beta-ocimene 27.2% in S. nutans and 34.9% in S. sericea, fenchyl acetate 12.7% in S. chlorantha, beta-linalool 40.5% in S. chlorantha and 14.5% in S. italica). Relatively high amounts of lilac compounds occur in S. latifolia (49.1%), Silene otites (35.7%), S. subconica (15.2%), and S. vulgaris (59.6%). Higher amounts of sesquiterpenes (isoprenoids) were only found in Silene vallesia with beta-bourbonene and gamma-muurolene. The vast majority of chemicals identified are common components of a wide array of scented angiosperm flowers. Nevertheless, the results conform most strongly with the findings in other night-blooming and/or moth-pollinated flowers. All investigated Silene species follow the general trend of floral scent compounds typical for moth-pollinated flowers, i.e. flowers having acyclic terpene alcohols (e.g. linalool), aromatic alcohols (benzyl alcohol, 2-phenylethanol) and esters derived from them, and small amounts of nitrogen-containing compounds. (C) 2002 Elsevier Science Ltd. All rights reserved.

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