Impact of invasive species Parectopa robiniella (Gracillariidae) on fluorescence parameters of Robinia pseudoacacia in the conditions of the steppe zone of Ukraine
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Published:2022-07-08
Issue:3
Volume:13
Page:324-330
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ISSN:2520-2588
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Container-title:Regulatory Mechanisms in Biosystems
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language:
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Short-container-title:Regul. Mech. Biosyst.
Author:
Holoborodko K. K.,Sytnyk S. A.,Lovynska V. M.,Ivanko I. A.,Loza I. M.,Brygadyrenko V. V.
Abstract
Robinia pseudoacacia L. is one of the most common and environmentally adaptable introduced tree species which has become an important element of artificial afforestation and landscaping in Ukraine over the past 150 years. Throughout the history of its introduction on the territory of Ukraine, this species was considered resistant because of the absence of dangerous phytophages. At the beginning of the XXI century, the phytosanitary situation changed as the result of the penetration and rapid spread of a number of North American invasive phytophages. The appearance and distribution of the miner Parectopa robiniella (Clemens, 1863) (Lepidoptera, Gracillariidae) feeding on R. pseudoacacia was recognized as the largest invasion in Ukraine. This paper considers the issues of studying the effect of P. robiniella caterpillars feeding on R. pseudoacacia in various forest-growing conditions in the steppe zone of Ukraine. The process of photosynthesis, as the most important physiological parameter, was chosen as indicator of condition. The study was conducted using biosensor technology which made it possible to measure the effect of caterpillar feeding on critical parameters of chlorophyll fluorescence (the Kautsky curve). The research has shown that the initial value of fluorescence induction was within the range of 196–284 RFU, and the maximum value of the background fluorescence parameter was recorded in undamaged leaves and under shading conditions. Both the effect of phytophages and the shading factor caused a significant decrease in the values of fluorescence induction of the “plateau” both in the conditions of an artificially washed sandbar, on the watershed area of a watershed-gully landscape, as well as on natural sandy-loam soil. The maximum values of photosynthetic fluorescence induction under the simultaneous influence of the studied factors had rather high variability. In contrast to the fluorescence induction parameter, the “plateau” of the highest maximum fluorescence induction was reached in the absence of pest damage under conditions of total shading. As revealed by dispersion and regression analyses, the maximum fluorescence index was most dependent on the amount of solar radiation and on the degree of the leaf surface damage by phytophages. Significantly higher values of the steady-state fluorescence induction parameter were determined in the absence of insect damage in both shading and lighting conditions. A statistically significant combined influence of abiotic and biotic factors on the “plateau” fluorescence induction parameter was determined in comparison with the mono-influence of individual factors. A highly significant dependence of the maximum efficiency indicator of primary photosynthesis processes on individual factors of exogenous influence was established, while the combined effect of these factors did not affect this parameter. The obtained data allow one to apply in practice the methods of analyzing chlorophyll fluorescence induction to establish the physiological state of tree flora in forest and garden farms.
Publisher
Oles Honchar Dnipropetrovsk National University
Subject
Toxicology,Pharmacology,Microbiology,Physiology,Cell Biology,Biophysics,Biochemistry,Biochemistry, Genetics and Molecular Biology (miscellaneous)
Reference62 articles.
1. Antal, T., Konyukhov, I., Volgusheva, A., Plyusnina, T., & Rubin, A. (2018). Chlorophyll fluorescence induction and relaxation system for the continuous monitoring of photosynthetic capacity in photobioreactors. Physiologia Plantarum, 165, 476–486. 2. Baranovski, B., Roschina, N., Karmyzova, L., & Ivanko, I. (2018). Comparison of commonly used ecological scales with the Belgard plant ecomorph system. Biosystems Diversity, 26(4), 286–291. 3. Brygadyrenko, V. V. (2015). Influence of moisture conditions and mineralization of soil solution on structure of litter macrofauna of the deciduous forests of Ukraine steppe zone. Visnyk of Dnipropetrovsk University, Biology, Ecology, 23(1), 50–65. 4. Brygadyrenko, V. V., & Nazimov, S. S. (2015). Trophic relations of Opatrum sabulosum (Coleoptera, Tenebrionidae) with leaves of cultivated and uncultivated species of herbaceous plants under laboratory conditions. Zookeys, 481, 57–68. 5. Bucher, S. F., Bernhardt-Römermann, M., & Römermann, C. (2018). Chlorophyll fluorescence and gas exchange measurements in field research: An ecological case study. Photosynthetica, 56, 1161–1170.
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