Specific features of the water regime of the genus Chaenomeles introduced plants in the steppe zone conditions

  • Y. V. Lykholat Oles Honchar Dnipro National University
  • V. R. Davydov Oles Honchar Dnipro National University
  • N. O. Khromykh Oles Honchar Dnipro National University
  • O. O. Didur Oles Honchar Dnipro National University
Keywords: chaenomeles, water deficit, transpiration intensity, drought, adaptation


Sufficient water supply for plants is one of the most important conditions for their vital activity, since most of the biochemical reactions that regulate the plants physiological functions take place in the water environment. The plants adaptive capacity to the influence of a complex of environmental factors in field conditions is largely determined by the ability to maintain water balance, which can be characterized by various features. Among them, the transpiration intensity and the level of water deficit are the most important indicators that are related to the mechanisms of plant resistance to water or high-temperature stress. The aim of the work was to evaluate the introduction success of plants according to the markers of water availability in a new environment. The objects of the study were plants of the genus Chaenomeles, introduced in the Botanical Garden of Oles Honchar Dnipro National University: three natural species (Ch. japonica, Ch. speciosa, and Ch. cathayensis), as well as two hybrids (Ch. × superba and Ch. × californica). Species Ch. japonica naturally grows in humid areas with moderate temperatures, while species of Chinese origin Ch. speciosa and Ch. cathayensis are adapted to mountainous terrain with sharp temperature fluctuations. Water deficiency in the leaves of introduced plants was determined by saturating leaf cuttings with water; the intensity of transpiration was studied by the method of rapid weighing. Both indicators of the water regime in the leaves of introduced plants were measured under contrasting levels of moisture supply during the growing season in the steppe zone conditions: in the wet period, the dry period, and the period of moisture restoration. It was found that during the drought, the intensity of transpiration increased significantly (P ˂ 0.05) compared to the wet period in the leaves of all introduced Chaenomeles plants, the most (by 1.6–1.7 times) in Ch. japonica, Ch. speciosa and Ch. × superba, the least (by 1.3 times) in the leaves of Ch. × californica. Water deficit in the dry growing season in the leaves of all studied Chaenomeles plants increased significantly (P ˂ 0.05), the most in the leaves of Ch. catayensis (2.8 times compared to the wet period), the least in the leaves of Ch. spesiosa (in 2.0 times compared to the wet period). The level of water deficit in the leaves of both Chinese species was lower than that of Ch. japonica (18.85%). In the leaves of Ch. japonica, Ch. speciosa and Ch. × superba was the fastest recovery of the water balance after drought, as well as the most effective regulation of the transpiration intensity level with the onset of drought and during the recovery period. Introduced plants of the species Ch. japonica, Ch. speciosa and Ch. × superba turned out to be the most adapted to vegetation in the conditions of the steppe climate, which is characterized by periods of drought.


Baranowska-Bosiacka, I., Bosiacka, B., Rast, J., Gutowska, I., Wolska, J., Rкbacz-Maron, E., Dкbia, K., Janda, K., Korbecki, J., & Chlubek, D. (2017). Macro- and microelement content and other properties of Chaenomeles japonica L. fruit and protective effects of its aqueous extract on hepatocyte metabolism. Biological Trace Element Research, 178(2), 327–337.

Bessonova, V. P. (2006). Praktykum z fiziolohii roslyn [Workshop on plant physiology]. Publishing Department of DSАU, Dnipropetrovsk (in Ukrainian).

Bieniasz, M., Dziedzic, E., & Kaczmarczyk, E. (2017). The effect of storage and processing on vitamin C content in Japanese quince fruit. Folia Horticulturae, 29(1), 83–93.

Brglez Mojzer, E., Knez Hrnčič, M., Škerget, M., Knez, Ž., & Bren, U. (2016). Polyphenols: Extraction Methods, Antioxidative Action, Bioavailability and Anticarcinogenic Effects. Molecules (Basel, Switzerland), 21(7), 901.

Danilchuk, N. M. & Danilchuk, O. V. (2018). Osoblyvosti sezonnoi dynamiky vodoobminnykh protsesiv u vydiv rodu Populus L. u dendrarii Kryvorizkoho botanichnoho sadu [Peculiarities  of  seasonal  dynamics  of  water-exchange  processes in species of Populus L. in dendrarium of Kryvyi Rih Botanical Garden]. Plant Introduction, 2(78), 92–101 (in Ukrainian).

Dolhova, L. H., Demura, T. A., & Koval, I. V. (2003). Osoblyvosti vodnoho obminu roslyn-introdutsentiv rodu Rosa L. [Peculiarities of water metabolism of introduced plants of the genus Rosa L.]. Visnyk of Dnipropetrovsk University. Biology, ecology, 11(2), 28–32 (in Ukrainian).

Du, H., Wu, J., Li, H., Zhong, P. X., Xu, Y. J., Li, C. H., Ji, K. X., & Wang, L. S. (2013). Polyphenols and triterpenes from Chaenomeles fruits: chemical analysis and antioxidant activities assessment. Food Chemistry, 141, 4260–4268.

Gao, F., Pei, S., Yang, L., Zuo, K., & Sun, S. (2011). Preliminary ethnobotanical study on Chaenomeles Lindl. of Yunnan. Journal of Anhui Agricultural Science, 7, 3950–3954.

Gorlach, S., Wagner, W., Podsędek, A., Szewczyk, K., Koziołkiewicz, M., & Dastych, J. (2011). Procyanidins from Japanese quince (Chaenomeles japonica) fruit induce apoptosis in human colon cancer Caco-2 cells in a degree of polymerization-dependent manner. Nutrition and cancer, 63(8), 1348–1360.

Grigoryuk, I. A., Tkachev, V. I., & Savinskiy, S. V. (2003). Sovremennyye metody issledovaniya i otsenki zasukho- i zharoustoychivosti rasteniy [Modern methods of research and evaluation of drought resistance and heat resistance of plants]. Naukovyi svit, Kyiv (in Russian).

Hamauzu, Y., Inno, T., Kume, C., Irie, M., & Hiramatsu, K. (2006). Antioxidant and antiulcerative properties of phenolics from Chinese quince, quince, and apple fruits. Journal of agricultural and food chemistry, 54(3), 765–772.

Khromykh, N., Lykholat, Y., Shupranova, L., Kabar, A., Didur, O., Lykholat, T., & Kulbachko, Y. (2018). Interspecific differences of antioxidant ability of introduced Chaenomeles species with respect to adaptation to the steppe zone conditions. Biosystems Diversity, 26(2), 132–138.

Kim, D. H., Subedi, L., Kim, H. R., Choi, S. U., Kim, S. Y., & Kim, C. S. (2021). Phenolic constituents of chinese quince twigs (Chaenomeles sinensis Koehne) and their anti-neuroinflammatory, neurotrophic, and cytotoxic activities. Antioxidants, 10, 551.

Klimenko, S. V., & Nedviga, O. M. (1999). Khenomeles: introduktsiya. sostoyaniye i perspektivy kultury [Flowering quince: introduction, present condition and prospects of the culture]. Plant Unroduction, 3–4, 125–134 (in Russion).

Krivoruchko, A., & Bessonova, V. (2017). Characteristics of the water exchange of the leaves of Quercus robur L. and Quercus rubra L. in pure and mixed groups. Stiinta agricola, 1, 66–73 (in Russian).

Lewandowska, U., Szewczyk, K., Owczarek, K., Hrabec, Z., Podsędek, A., Koziołkiewicz, M., & Hrabec, E. (2013). Flavanols from Japanese quince (Chaenomeles japonica) fruit inhibit human prostate and breast cancer cell line invasiveness and cause favorable changes in Bax/Bcl-2 mRNA ratio. Nutrition and cancer, 65(2), 273–285.

Liashok, A. K., Hryhoriuk, I. P., Feoktisov, P. O. (2006). Avtokolyvalni protsesy vodoobminu roslyn [Self-oscillating processes of water exchange in plants]. Logos, Kyiv (in Ukrainian).

Lingdi, L., Cuizhi, G., Chaoluan, L., Alexander, C., Bartholomew, B., Brach, A. R., Boufford, D. E., Ikeda, H., Ohba, H., Robertson, K. R., Spongberg, S. A. (2003). Rosaceae. In Wu Zheng-Yi, Peter H. Raven, Hong De-Yuan (Eds.). Flora of China, Volume 9: Pittosporaceae throug h Connaraceae. Missouri Botanical Garden Press, St. Louis. P. 46–434.

Loutfy, M. H. A., El-Mashad. A. A. A., & Kamel E. A. (1999). Studies in the Maloideae (Rosaceae) I – Chaenomeles Lindley and Cydonia Miller. Taeckholmia, 19(2), 97–114.

Lykholat, Y. V. (1999). Ekoloho-fiziolohichni osoblyvosti bahatorichnykh dernoutvoriuiuchykh zlakiv tekhnohennykh terytorii [Ecological and physiological features of perennial sod-forming cereals of technogenic territories]. Dnipropetrovsk University Press, Dnipropetrovsk (in Ukrainian).

Lykholat, Y. V. (2003). Vodnyi obmin dernoutvoriuiuchykh trav, shcho zrostaiut u shtuchnykh fitotsenozakh [Water exchange of sod-forming grasses growing in artificial phytocenoses]. Visnyk Donetskoho universytetu. Ser. A. Pryrodnychi nauky, 1, 288–290 (in Ukrainian).

Lykholat, Y. V., Khromykh, N. O., Lykholat, T. Y., Didur, O. O., Lykholat, O. A., Legostaeva, T. V., Kabar, A. M., Sklyar, T. V., Savosko, V. M., Kovalenko, I. M., Davydov, V. R., Bielyk, Y. V., Volyanik, K. O., Onopa, A. V., Dudkina, K. A., & Grygoryuk, I. P. (2019). Industrial characteristics and consumer properties of Chaenomeles Lindl. fruits. Ukrainian Journal of Ecology, 9(3), 132–137.

Ma, Y., Li, J., Li, J., Yang, L., Wu, G., & Liu, S. (2022). Comparative metabolomics study of Chaenomeles speciosa (Sweet) Nakai from different geographical regions. Foods (Basel, Switzerland), 11(7), 1019.

Miao, J., Li, X., Zhao, C., Gao, X., Wang, Y., & Gao, W. (2018). Active compounds, antioxidant activity and alpha-glucosidase inhibitory activity of different varieties of Chaenomeles fruits. Food Chemistry, 248, 330–339.

Miao, J., Zhao, C., Li, X., Chen, X., Mao, X., Huang, H., Wang, T., & Gao, W. (2016). Chemical composition and bioactivities of two common chaenomeles fruits in China: Chaenomeles speciosa and Chaenomeles sinensis. Journal of food science, 81(8), H2049–H2058.

Moskalets, T. Z., Moskalets, V. V., Vovkohon, A. H., Shevchuk, O. A., & Matviichuk, O. A. (2019). Modern breeding and cultivation of unpopular fruits and berries in Ukraine. Ukrainian Journal of Ecology, 9(3), 180–188.

Musiienko, M. M. (2005). Fiziolohiia roslyn [Physiology of plants]. Lybid, Kyiv (in Ukrainian).

Owczarek, K., Hrabec, E., & Fichna, J. (2017). Flavanols from Japanese quince (Chaenomeles japonica) fruit suppress expression of cyclooxygenase-2, etalloproteinase-9, and nuclear factor-kappaB in human colon cancer cells. Acta Biochimica Polonica, 6(3), 567–576.

Ponomaryova, O. A. (2011). Vodnyi obmin derev rodu Tilia L. v umovakh stepovoi zony Ukrainy [Water exchange of trees of genus Tilia L. in the conditions of a steppe zone of Ukraine]. Visnyk Dnipropetrovskoho derzhavnoho ahrarnoho universytetu, 2, 46–50 (in Ukrainian).

Rumpunen K. (2002). Chaenomeles: Potential new fruit crop for Northern Europe. In J. Janick, A. Whipkey (Eds.), Trends in new crops and new uses (pp. 385–392). Alexandria, ASHS Press.

Shen, T., Hu, F., Liu, Q., Wang, H., Li, H. (2020). Analysis of flavonoid metabolites in chaenomeles petals using UPLC-ESI-MS/MS. Molecules, 25 (17), 3994.

Strugała, P., Cyboran-Mikołajczyk, S., Dudra, A., Mizgier, P., Kucharska, A. Z., Olejniczak, T., & Gabrielska, J. (2016). Biological activity of japanese quince extract and its interactions with lipids, erythrocyte membrane, and human albumin. The Journal of membrane biology, 249(3), 393–410.

Thomas, M., Guillemin, F., Guillon, F., & Thibault, J.-F. (2003). Pectins in the fruits of Japanese quince (Chaenomeles japonica). Carbohydrate Polymers, 53(4), 361–372.

Watychowicz, K., Janda, K., Jakubczyk, K., & Wolska, J. (2017). Chaenomeles – health promoting benefits. Roczniki Panstwowego Zakladu Higienym 68(3), 217–227.

Yang, L., Ahmed, S., Stepp, J. R., Zhao, Y., Zeng, M. J., Pei, S., Xue, D., & Xu, G. (2015). Cultural uses, ecosystem services, and nutrient profile of flowering quince (Chaenomeles speciosa) in the highlands of Western Yunnan, China. Economic Botany, 69(3), 273–283.

Zaitceva, I. O. (2017). Kilkisna otsinka posukhostiikosti introdutsentiv rodu Syringa L. v umovakh stepovoho Prydniprovia [Quantitative estimation of drought-resistance of introduced plants genus Syringa L. in steppe right bank of Dnipro]. Issues of steppe forestry and forest reclamation of soils, 46, 76–81 (in Ukrainian).

Zakłos-Szyda, M., & Pawlik, N. (2018). Japanese quince (Chaenomeles japonica L.) fruit polyphenolic extract modulates carbohydrate metabolism in HepG2 cells via AMP-activated protein kinase. Acta biochimica Polonica, 65(1), 67–78.

Zandalinas, S. I., Mittler, R., Balfagón, D., Arbona, V., & Gómez-Cadenas, A. (2018). Plant adaptations to the combination of drought and high temperatures. Physiologia plantarum, 162(1), 2–12.

Zhang, R., Li, S., Zhu, Z., & He, J. (2019). Recent advances in valorization of Chaenomeles fruit: A review of botanical profile, phytochemistry, advanced extraction technologies and bioactivities. Trends in Food Science & Technology, 91, 467–482.

Zhang, S. Y., Han, L. Y., Zhang, H., & Xin, H. L. (2014). Chaenomeles speciosa: A review of chemistry and pharmacology. Biomedical reports, 2(1), 12–18.

Zhang, X., Bian, Z., Li, S., Chen, X., & Lu, C. (2019). Comparative analysis of phenolic compound profiles, antioxidant capacities, and expressions of phenolic biosynthesis-related genes in soybean microgreens grown under different light spectra. Journal of Agricultural and Food Chemistry, 67(49), 13577–13588.

Zhuk, О. І. (2011). Formuvannia adaptyvnoi vidpovidi roslyn na defitsyt vody [Formation of plant adaptive response on water deficit]. Fiziologiya i biokhimiya kulturnykh rasteniy, 43(1), 26–37 (in Ukrainian).

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Lykholat, Y., Davydov, V., Khromykh, N., & Didur, O. (2022). Specific features of the water regime of the genus Chaenomeles introduced plants in the steppe zone conditions. Ecology and Noospherology, 33(1), 9-14. https://doi.org/https://doi.org/10.15421/032202