Journals / Turkish Journal of Botany / 2014 / Cilt: 38 - Sayı: 5

Flower closure in the feld bindweed ( Convolvulus arvensis): a feld test of the pollination hypothesis

Pages
877–882
Publication Date
2022-11-05
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Collectively, our results suggest that feld bindweed fowers respond to pollination adaptively, because prolonged fowerlongevity may increase the likelihood of successful pollination and fower closure reduces energy spent on fower maintenance and/orintraspecifc competition with genetically familiar fowers.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Although the behavioral plasticity of fower traits has received considerable attention, its adaptive value is not thoroughlyunderstood.
📊
Key Findings & Data:We experimentally examined fower opening/closure in feld bindweed (Convolvulus arvensis), a species with short fowerpersistence (1 day) in which adaptive responses to pollination were not previously expected.
💡
Conclusion & Impact:Collectively, our results suggest that feld bindweed fowers respond to pollination adaptively, because prolonged fowerlongevity may increase the likelihood of successful pollination and fower closure reduces energy spent on fower maintenance and/orintraspecifc competition with genetically familiar fowers.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Although the behavioral plasticity of fower traits has received considerable attention, its adaptive value is not thoroughlyunderstood. We experimentally examined fower opening/closure in feld bindweed (Convolvulus arvensis), a species with short fowerpersistence (1 day) in which adaptive responses to pollination were not previously expected. In line with the pollination hypothesis wesuggested that fower exposure in this species should respond to pollination. More specifcally, we predicted that fower closure in thepollinated fowers would be quicker than that in unpollinated fowers. As predicted, the unpollinated fowers were open for a longertime than the pollinated fowers. Tere was no diference, however, between the self- and cross-pollinated fowers in terms of fowerlongevity. Tere was an inverse relationship between fower longevity and fertility, which also suggests that pollination leads to reducedfower longevity. Collectively, our results suggest that feld bindweed fowers respond to pollination adaptively, because prolonged fowerlongevity may increase the likelihood of successful pollination and fower closure reduces energy spent on fower maintenance and/orintraspecifc competition with genetically familiar fowers. Te behavioral plasticity of fower closure does not seem to be restricted onlyto plants with high fower longevity.

🔖

Cite This Article

PROKOP, P., NEUPAUEROVA, D. (2022). Flower closure in the feld bindweed ( Convolvulus arvensis): a feld test of the pollination hypothesis. Turkish Journal of Botany, Cilt: 38 - Sayı: 5, 877–882. https://ajindex.com/articles/601086

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (1)

  1. Abdala Robers L, Parra Tabla V, Navarro J (2007). Is foral longevity infuenced by reproductive costs and pollination success in Cohniella ascendens (Orchidaceae)? Ann Bot 100: 1367–1371. Ashman TL, Schoen DJ (1994). How long should fowers live? Nature 371: 788–791. Berjano R, Arista M, Talavera M, Ariza MJ, Ortiz PL (2014). Plasticity and within plant sex-ratio variation in monoecious Emex spinosa. Turk J Bot 38: 258–267. Betini GS, Norris DR (2012). Te relationship between personality and plasticity in tree swallow aggression and the consequences for reproductive success. Anim Behav 83: 137–143. Brys R, Jacquemyn H (2011). Variation in the functioning of autonomous self-pollination, pollinator services and foral traits in three Centaurium species. Ann Bot 107: 917–925. Clark MJ, Husband BC (2007). Plasticity and timing of fower closure in response to pollination in Chamerion angustifolium (Onagraceae). Int J Plant Sci 168: 619–625. Dafni A, Firmage D (2000). Pollen viability and longevity: practical, ecological and evolutionary implications. Pl Syst Evol 222: 113–132. De Kroon H, Huber H, Stuefer JF, van Groenendael JM (2005). A modular concept of phenotypic plasticity in plants. New Phytol 166: 73–82. Dingemanse NJ, Wolf M (2013). Between-individual diferences in behavioural plasticity within populations: causes and consequences. Anim Behav 85: 1031–1039. Ferval M, Legal L, Gers C, Pelissier C, Winterton P, Sanchez Lopez JA, Corona Rangel ML, Torres KB (2013). When island-like populations at high elevation show genetic divergence despite no morphological variability: the case of Lupinus montanus in Central Mexico. Turk J Bot 37: 789–801. Frederickson ME, Ravenscraf A, Hernández LMA, Booth G, Astudillo V, Miller GA (2013). What happens when ants fail at plant defence? Cordia nodosa dynamically adjusts its investment in both direct and indirect resistance traits in response to herbivore damage. J Ecol 101: 400–409. Fründ J, Carsten F, Dormann CF, Tscharntke T (2011). Linne’s foral clock is slow without pollinators —fower closure and plant- pollinator interaction webs. Ecol Lett 14: 896–904. Fürstenberg Hägg J, Zagrobelny M, Bak S (2013). Plant defense against insect herbivores. Int J Mol Sci 14: 10242–10297. Gagliano M (2013). Green symphonies: a call for studies on acoustic communication in plants. Behav Ecol 24: 789–796. Gianoli E (2004). Plasticity of traits and correlations in two populations of Convolvulus arvensis (Convolvulaceae) difering in environ