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Morphological and chemical characteristics of Fritillaria species: species differentiation through morphometric measurements and GC-MS analysis

Published online by Cambridge University Press:  08 January 2025

Bengisu Şentürk
Affiliation:
Faculty of Science, Department of Biology, Ondokuz Mayıs University, Samsun 55139, Türkiye
Erdi Can Aytar*
Affiliation:
Faculty of Agriculture, Department of Horticulture, Usak University, Uşak 64200, Türkiye
Alper Durmaz
Affiliation:
Nihat Gökyigit Botanical Garden Application and Research Center, Artvin Çoruh University, Artvin 08000, Türkiye
Sinan İşler
Affiliation:
Faculty of Education, Department of Science and Mathematics, Van Yuzuncu Yıl University, Van 65080, Türkiye
İsmail Gökhan Deniz
Affiliation:
Faculty of Education, Department of Biology Education, Akdeniz University, Antalya 07058, Türkiye
Yasemin Özdener Kömpe
Affiliation:
Faculty of Science, Department of Biology, Ondokuz Mayıs University, Samsun 55139, Türkiye
*
Corresponding author: Erdi Can Aytar; Email: erdi.aytar@usak.edu.tr

Abstract

This study examines the morphological and chemical characteristics of seeds from five Fritillaria species: Fritillaria pinardii, Fritillaria pontica, Fritillaria kittaniae, Fritillaria imperialis and Fritillaria alfredae Post subsp. glaucoviridis (Turrill) Rix. Morphological measurements included total length, total width, embryo length, embryo width, seed left-wing coverage width, seed right-wing coverage width and the distance between crossing points. These measurements revealed significant differences among the species. For example, F. imperialis exhibited the longest seeds and the largest embryos, while F. alfredae Post subsp. glaucoviridis had the smallest dimensions. Chemical analyses were conducted using gas chromatography-mass spectrometry, identifying various significant compounds across the species. High proportions of 2,2-dimethoxybutane were found in the seed samples. In F. pontica, compounds such as 2,2-dimethoxybutane (66.33%) and 1,1-dipropoxypropane (13.24%) were prevalent. Fritillaria kittaniae seeds showed high levels of benzene, 1,1′-(3,3-dimethyl-1-butenylidene) bis- (25.57%) and cyclohexene, 3-methyl-6-(1-methylethylidene)- (6.89%). In F. imperialis, significant compounds included 1,3-dioxolane-4-methanol, 2-ethyl-2-methyl (9.73%) and dodecane (5.73%). Fritillaria pinardii had notable amounts of 3,6-dimethyloctane (4.81%), while F. alfredae subsp. glaucoviridis contained 2-methoxyethyl(trimethyl)silane (13.21%). Principal component analysis and cluster analysis revealed clear groupings based on morphological and chemical similarities. Fritillaria pinardii, F. pontica and F. kittaniae formed a cluster due to their similar morphological and chemical characteristics, whereas F. imperialis and F. alfredae subsp. glaucoviridis formed a distinct group. These findings provide valuable insights into the identification and classification of Fritillaria species. Integrating morphological and chemical data can enhance the accurate identification of these species. This study contributes to understanding the natural diversity of Fritillaria species and has implications for ecological studies.

Type
Research Article
Copyright
Copyright © The Author(s), 2025. Published by Cambridge University Press on behalf of National Institute of Agricultural Botany

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References

Advay, M, Tekşen, M and Maroofi, H (2015) Fritillaria avromanica sp. nov. (Liliaeceae) from Iran and notes on F. melananthera in Turkey. Nordic Journal of Botany 33, 526531.CrossRefGoogle Scholar
Advay, M, Rix, M and Tekşen, M (2022) Fritillaria kordestanica (Liliaceae), a new species from western Iran. Phytotaxa 554, 7076.CrossRefGoogle Scholar
Aslay, M, Yıldız, F, Kaya, O and Bita-Nicolae, C (2023) Reproductive biology and pollination ecology of Fritillaria michailovskyi Fomin (Liliaceae), endemic to East Anatolia (Turkey). Diversity 15, 414.CrossRefGoogle Scholar
Aytar, EC, Harzli, I and Kömpe, (2023) Phytochemical analysis of Anacamptis coriophora plant cultivated using ex vitro symbiotic propagation. Chemistry & Biodiversity 20, e202301218.CrossRefGoogle ScholarPubMed
Borjigin, G, Wei, F, Jiang, S, Li, Q and Yang, C (2023) Extraction, purification, structural characterization and biological activity of polysaccharides from Fritillaria: a review. International Journal of Biological Macromolecules 242, 124817.CrossRefGoogle ScholarPubMed
da Silva, LP, Ramos, JA, Olesen, JM, Traveset, A and Heleno, RH (2014) Flower visitation by birds in Europe. Oikos 123, 13771383.CrossRefGoogle Scholar
Duman, H and Tekşen, M (2024) Fritillaria ozgeana (Liliaceae), a new yellow-flowered species from SW Anatolia. Annales Botanici Fennici Turkey 61, 189198.Google Scholar
Eker, İ and Tekşen, M (2023) Fritillaria umitkaplanii (Liliaceae), a new species from south Anatolia. Nordic Journal of Botany 2023, e03803.CrossRefGoogle Scholar
Hajihashemi, S, Brestic, M, Landi, M and Skalicky, M (2020) Resistance of Fritillaria imperialis to freezing stress through gene expression, osmotic adjustment and antioxidants. Scientific Reports 10, 113.CrossRefGoogle ScholarPubMed
Kiani, M, Mohammadi, S, Babaei, A, Sefidkon, F, Naghavi, M, Ranjbar, M, Razavi, SA, Saeidi, K, Jafari, H, Asgari, D and Potter, D (2017) Iran supports a great share of biodiversity and floristic endemism for Fritillaria spp. (Liliaceae): a review. Plant Diversity 39, 245262.CrossRefGoogle ScholarPubMed
Luo, M, Gao, J, Liu, R, Wang, SQ and Wang, G (2023) Morphological and anatomical changes during dormancy break of the seeds of Fritillaria taipaiensis. Plant Signaling & Behavior 18, 2194748.CrossRefGoogle ScholarPubMed
Ma, B, Ma, J, Li, B, Tao, G, Gan, J and Yan, Z (2021) Effects of different harvesting times and processing methods on the quality of cultivated Fritillaria cirrhosa D. Don. Food Science & Nutrition 9, 28532861.CrossRefGoogle Scholar
Peruzzi, L, Leitch, IJ and Caparelli, KF (2009) Chromosome diversity and evolution in Liliaceae. Annals of Botany 103, 459475.CrossRefGoogle ScholarPubMed
POWO (2024) See Available at https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:30008840-2 (accessed 29 September 2024).Google Scholar
Qi, P, Zhang, Y, Zhao, C, Sun, L, Bai, R, Wang, L and Sun, C (2023) Research progress on biological regulation and biosynthesis of isosteroid alkaloids in Fritillaria. Plant Growth Regulation 101, 599615.CrossRefGoogle Scholar
Samaropoulou, S, Bareka, P, Bouranis, DL and Kamari, G (2019) Seed morphology in the genus Fritillaria (Liliaceae) from Greece and its taxonomic significance. Phytotaxa 416, 223237.CrossRefGoogle Scholar
Samaropoulou, S, Bareka, P and Kamari, G (2020) Hybridization and karyotype variability of three endemic Fritillaria L. (Liliaceae) in Argolis Peninsula (Greece). Plant Biosystems – An International Journal Dealing with all Aspects of Plant Biology 154, 348360.CrossRefGoogle Scholar
Tatarenko, I, Walker, K and Dyson, M (2022) Biological Flora of Britain and Ireland: Fritillaria meleagris. Journal of Ecology 110, 17041726.CrossRefGoogle Scholar
Wang, SH, Wang, YQ, Wang, QQ, Wang, L, Zhang, QY and Tu, PF (2023) Steroidal alkaloids from the bulbs of Fritillaria unibracteata var. wabuensis and their anti-inflammatory activities. Phytochemistry 209, 113640.CrossRefGoogle ScholarPubMed