SUMMARY
The effect of altitude-associated environmental gradient on leaves metabolic features of Quercus robur L. (an oak) and Fraxinus excelsior L. (an ash) was investigated in the natural coastal forest at Bellegarde' International Biosphere Reserve in Steppe zone, Ukraine. Decrease in relative humidity contrary to increase in temperature and lighting under the forest canopy were observed on the river steep bank with altitudinal elevation from lower (52 m a.s.l.) to middle (74 m.), and upper (96 m). Responses of tree leaves photosynthetic and antioxidant systems to the environmental local changes were studied by measuring chlorophyll (Chl) content, as well as catalase and peroxidase activities. Decrease in Chl amount in the ash leaves at middle and upper altitudes (17 and 38% compared with lower), along with increase (8% and 13%, respectively) in the oak leaves was found out. Chl content was determined to correlate with light, temperature, and humidity in both leaves of ash (respectively, r = - 0.94, r = - 0.92, r = 0.90) and oak (r = 0.95, r = 0.93, r = - 0.90). Catalase activity grew with increasing altitude in leaves of ash (2 and 2.2 fold compared to lower altitude) and oak (1.2 and 1.4 fold) as well. Contribution of catalase to the total antioxidant enzymes activity enhanced in leaves of both species with increasing altitude. The results confirmed high sensitivity of steppe forest trees even to slight altitude-associated environmental deviations. Data obtained can be used to assess the adaptive potential of woody species to the climate changes aiming towards greater aridity traits and select tree species for planted forest creation as well.
Keywords: Quercus robur L., Fraxinus excelsior L., altitude, microclimate, enzymes.
INTRODUCTION
Ecological and economic importance of the forests worldwide necessitates their conservation under climatic changes tending to aridity features enhancement (Bussotti et al., 2015), and determines relevance of trees adaptive capabilities studying. Talbi et al. (2015) suggest the exacerbation of plants survival problem with increased drought in numerous areas throughout the world, especially in the arid regions. Bussotti et al. (2015) state that due to increasing temperature and drought southern genotypes are likely to replace forest species in Western and Central Europe. Mokria et al. (2015) agree that namely climatic changes, in particular heat increase, might have contributed to forest dieback in northern Ethiopia. It's noteworthy that El-Hajj et al. (2014) emphasize probable severe consequences of the climatic deviations for the forest ecosystems despite plodding effect and small range of changes.
Natural forest conservation and restoration appears as a significant problem for Ukraine. The percentage of forest land in our country reaches 16.0% (Tkach, 2012). This index is one of the lowest among European countries. It is known that Steppe zone occupies about 40% of Ukrainian territory. The forests distribution is complicated by unfavourable conditions of geographic mismatch for the forest ecosystems. Steppe climate is characterized by the seasonal drought periods accompanied by high temperature and dry winds. Average annual rainfall is 472 mm, while in dry years 250 mm only; the annual amount of evaporation exceeds the precipitation by 2-3 times. Existence of the plant forest communities in the Steppe zone is possible due to geomorphologic diversity which enables formation of special local environmental conditions in the steep rivers banks. The steppe forest ecosystems may be highly sensitive to any environmental deviations under such circumstances. According to Ramirez-Valiente et al. (2015), climate is a major selective force in nature.
Plant responses and adaptation to the environmental conditions are complex biological processes including physiological and biochemical changes (Harfouche et al., 2014; Granda et al., 2014; Parviz, 2016). The mechanism of tree metabolic adaptation to local environmental factors is an important aspect of the overall forest conservation problem. It has been studied intensively during recent years. Thus, Aranda et al. (2015) showed significant physiological differences among six Fagus sylvatica populations adapted to specific local water availability. Zadworny et al. (2015) established a strong seasonal variation in nitrogen concentration among roots of oak trees growing in two contrasting soil types. Sperlich et al. (2015) showed differences in photosynthetic potentials and drought-tolerance in sunlit and shaded leaves of four Mediterranean trees. The significant impact of microclimate on transition processes to the generative phase of plant development was described by Bahuguna and Jagadish (2015). Next point is the study of the altitude impact on tree taxa distribution. Rezende et al. (2015) concluded that altitude belongs to major environmental parameters which can be used for developing a forest conservation strategy. The aim of our study - to estimate abiotic factors (local temperature, relative humidity and lighting) impact on photosynthetic and antioxidant systems of coastal forest trees Quercus robur L. (an oak) and Fraxinus excelsior L. (an ash) associated with the different river slope altitudes.
MATERIAL AND METHODS
Study area
The study was conducted in the territory of Bellegarde' Prisamarsky International Biosphere Reserve located in in the northen part of steppe zone in Dnipropetrovs'k province (47°32'-49°11'N, 33°-33°56'E). Studied areas are located on the southern slope of the Samara river. Observed plots are disposed in right steep bank at lower (52 m a.s.l.), middle (74 m a.s.l.), and upper (96 m a.s.l.) altitude in an old-growth (more than 85 years old) mixed deciduous natural forest. The plant community of the coastal forest is represented by several trees and shrubs with an oak (Quercus robur L.) and an ash (Fraxinus excelsior L.) dominating along the slope. Both the Q. robur and F. excelsior are the autochthonous and edificatory species of natural forest. The list of co-dominant species includes a linden (Tillia cordata Mill.), two species from Acer genus (Acer platanoides L. and Acer campestre L.), an elm (Ulmus laevis Pall.), and Corylus avellana (L.) H. Karst. The forest undergrowth is formed by Acer platanoides young trees, with shrub species Sambucus nigra L. and Euonymus europaeus L.
Data collection
Microclimate data within the studied area were collected during the period of trees vegetation (April-August 2015). Data on air temperature and relative humidity levels under the tree canopy were obtained with the help of a portable weather station equipped by Assmann psychrometer (model 225-5230, Germany). Lighting levels under canopy were measured with a luxmeter (model Y u16, Russia) at the height of 2 m which corresponds to the level of lowest trees branches. Simultaneously, lighting level in open areas at each studied altitude was measured. The leaves of Quercus robur and Fraxinus excelsior were collected in the mean of May 2015 from 3-5 same-age trees within three groups in each studied area, and frozen.
Data analysis
Chlorophyll content and antioxidant enzyme activities (catalase, guaiacol - peroxidase, and benzidine - peroxidase) were measured with spectrophotometric methods. Chlorophyll content (Chl a, Chl b, and total chlorophyll value) was measured according to the method of Wintermans and De Mots (1965) in the ethanol extracts of tree leaves, and expressed in mcg of chlorophyll per g fresh weight (mcg/g FW).
Antioxidant enzymes activities were determined in the supernatants obtained by centrifugation (15,000 g for 20 min and 4° C) of cru de extracts (100 mg of fresh leaves homogenized with 0.2 M TRIS-HCl buffer, pH 7.0 contained 0.1% polyvinylpyrrolidone, 250 mM saccharose, and 1 mM MgCl2). Catalase (CAT) activity was evaluated according to Goth (1991) by measurement at 410 nm of optical density of reactive mixture containing 0.2 ml sample, 0.1% H2O2, and 4% ammonium molibdate. The result was calculated through the calibration graph and expressed in mM H2O2/g FW. Activity of guaiacol-peroxidase (GPOD) was estimated in accordance with Ranieri et al. (2001) by detecting guaiacol oxidation at 470 nm in the reactive mixture containing acetate buffer (pH 6.0), 2 mM guaiacol, 0.2 ml sample, and 0.15% H2O2. The result was calculated with consideration of the guaiacol molar extinction coefficient, and expressed in mM guaiacol/g FW. Benzidine-peroxidase (BPOD) activity determination was based on the method proposed by Gregory (1966). Optical density change was registered for 1 min at 470 nm after adding 1% H2O2 to reactive mixture (acetate buffer, pH 6.0, 0.02 mM benzidine and 0.2 ml sample). The result was expressed in optical units/g FW.
All determinations of air temperature, relative humidity, and lighting (under tree canopy and in open areas) were performed in six replicates at each studied site. All determinations of the biochemical parameters characterizing the oak and ash leaves required five replicates. Data represent mean values and standard deviations (±SD).Differences significance was estimated using Student's t-test (P<0.05).
RESULTS AND DISCUSSION
The levels of temperature, relative humidity, and lighting under the forest canopy varied with the altitudinal elevation of the coastal slope, as shown in Table 1.
Increase in lighting reached 1.3 fold at the middle altitude and 2.4 fold at upper altitude compared to the lower (P<0.05). Air temperature increase as well as relative humidity reduction under the canopy occurred to have gradient character in the course of moving upwards on the slope. The given study defines these local changes of microclimate and lighting as a conventional enhancing aridity trait with increasing altitude. It is possible to see the plants physiological and biochemical responses to the environmental changes.
Total chlorophyll content and ratio of chlorophyll forms (Chl a/Chl b) varied depending on the altitude-associated microclimatic conditions both in the oak and ash leaves (Table 2). We observed that an increase in temperature and lighting along with decrease in relative humidity upward the slope accompanied by the growth of total chlorophyll content in Q. robur leaves at the middle and upper altitudes compared to the lower (respectively, 8% and 13%, P<0.05).
At the same time, reduction in chlorophyll amount (17% and 38% at the middle and upper altitudes compared to the lower, P<0.05) was found in leaves of F. excelsior. The results obtained are consistent with the notion (Ramirez-Valiente et al, 2015) that photosynthesis is one of most sensitive process to the environmental stresses. In particular, intensity of photosynthetic pigments biosynthetic pathway depends on lighting and moisture. In oak leaves, accumulation both of chlorophyll a and chlorophyll b contributed to the increase in total chlorophyll amount with altitudinal elevation. However, decrease in the ratio Chl a/Chl b indicates the heightened Chl b accumulation. In contrast, more significant reduction of chlorophyll b content was observed in ash leaves at the middle and upper altitudes, thereby increasing the ratio Chl a/Chl b. According to Caudle et al. (2014), high Chl a/Chl b ratio is an index of plant adaptation to drought. Thus, we assumed that the Quercus robur trees showed higher adaptability to relative humidity reduction, as well as complex environmental changes tending to enhance the aridity traits uphill the slope. Correlation analysis revealed strong positive coefficients between changes of Q. robur leaves total Chl content and temperature (r = 0.92) together with lighting (r = 0.86), whereas the interaction with relative humidity changes was negative (r = -0.86). On the contrary, leaves of F. excelsior showed a positive relationship between humidity and Chl content (r = 0.92), while correlation was getting negative in the course of temperature (r = -0.89) and lighting (r = -0.90) changes uphill. Hereof, the rate of Chl biosynthesis in oak leaves was stimulated by an increase in temperature and light despite the decrease in relative humidity; at the same time, Chl accumulation in ash leaves was oppressed due to environmental changes. These conclusions resonate with data by Caudle et al. (2014), according to which drought-tolerant species are able to maintain high intensity of photosynthesis and protect photosystem II during dry periods. In addition, our results coincide with data by Rajsnerova et al. (2015) on significant growth of the total Chl content in the lower leaves of Fagus sylvatica canopy just at the upper altitude and the highest light intensity.
The different changes in catalase and peroxidase activity followed the altitude- associated modifications of temperature, lighting, and relative humidity levels both in the leaves of Q. robur and F. excelsior (Table 3).
Significant decrease in BPOD activity was observed in oak leaves at the middle and upper altitudes compared to lower (1.4 and 3.7 folds respectively, P<0.05), while activity of GPOD tended to enhance at the middle altitude and decrease at the upper (1.3 and 2.2 folds respectively, P<0.05). In ash leaves decrease in BPOD activity was insignificant, whereas GPOD activity declined 2.9 folds (P<0.05) at the upper altitude compared to lower. Halliwell (2006) proclaims plant peroxidase functions to be associated with eliminating the excessive hydrogen peroxide accumulated during various physiological processes. Therefore, the results obtained indicate significant metabolic adjustment in oak and ash leaves in the course of slope altitude elevation and enhancing aridity. Probably, changes may affect the accumulation of phenols and sugars, since Allison and Schultz (2004) emphasized the peroxidases appear to play the important role in these metabolic pathways.
The catalase activity at the middle and upper altitudes exceeded the lower level both in the oak (1.2 and 1.4 folds respectively, P<0.05), and ash of leaves (respectively 2 and 2.2 folds, P<0.05). Together, the results showed increase in catalase proportion in the total antioxidant activity of tree leaves with growing altitude. This proportion in oak leaves varied from 68% at lower altitude to 77% at the middle and 91% at the upper. The catalase contribution in the leaves of ash was 11%, 22%, and 41% of total antioxidant activity respectively at the lower, middle and upper altitudes. Strong positive correlation between the catalase activity and lighting together with temperature was revealed in the leaves of oak (r = 0.83 and r = 0.93 respectively) and ash (r = 0.78 and r = 0.82). Thus, our data are consistent with the conclusion of Mhamdi et al. (2010) about high plant catalases sensitivity to light. In the whole, the above data showed a substantial growing catalase involvement in the antioxidant processes in leaves of .Q. robur and F. excelsior with increasing altitude and enhancing aridity traits. This conclusion is consistent with Queval's et al. (2007) opinion on the important plant catalase role in hydrogen peroxide elimination during photosynthesis as well as photorespiration stimulated by solar radiation and high temperature. Besides, the results obtained coincide with data by Mhamdi et al. (2010) that catalases are highly activated enzymes. It is an integral part of plant defense system. So, enchanting antioxidant protective capacity associated with catalase activation was revealed both in oak and ash leaves with increasing altitude of the slope and enhancing aridity. Comparing results of the our study with data by Rajsnerova et al. (2015) on the beech leaves metabolic changes due to significant altitude difference (400-1100 m), it is reasonable to mention high sensitivity of Quercus robur and Fraxinus excelsior leaves to the environmental changes, associated with smallest altitudinal elevation.
CONCLUSIONS
Results of present study confirmed the hypothesis of a high sensitivity of Quercus robur L. and Fraxinus excelsior L. metabolic processes to even small environmental differences with increasing altitude. Decrease in relative humidity along with increase in temperature and lighting under the forest canopy were assessed as a conventional increase in aridity up the slope. Significant catalase activation together with increasing enzyme contribution to the total antioxidant capacity was common trait both in oak and ash leaves. Species - determined differences in the metabolic changes were manifested in the variations of photosynthetic process. Accumulation of chlorophyll in oak leaves was stimulated by an increase in temperature and light in spite of the decrease in relative humidity; and it declined in ash leaves due to environmental changes. The results of study may be useful for assessing adaptive capacity of woody species to increased aridity, and species selection for further creation of forest plantations in the Steppe zone.
ACKNOWLEDGEMENTS
The present research was conducted under the grant of Ministry of Education and Science of Ukraine (N 0113U003034). Authors are grateful to the Biology Research Institute of Dnipropetrovs'k National University for the maintenance of the expedition to Biosphere Reserve.
REFERENCES
Allison, S.D. & Schultz, J.C. (2004).Differential activity of peroxidase isozymes in response to wounding, gypsy moth, and plant hormones in Northern red oak (Quercus rubra L.)", Journal of Chemical Ecology, vol. 30, no. 7, pp. 1363-1379
Aranda, I.., Cano, F.J., Gasco, A., Cochard, H.., Nardini, A.., Mancha, J.A., Lopez, R., Sanchez-Gomez, D. (2015). Variation in photosynthetic performance and Mhydraulic architecture across European beech (Fagus sylvatica L.) populations supports the case for local adaptation to water stress, Tree Physiology, vol. 35, no. 1, pp. 34-46
Bahuguna, R.N. & Jagadish, K.S.V. (2015) Temperature regulation of plant phenological development, Environmental and Experimental Botany, vol. 111, no. 3, pp. 83-90
Bussotti, F., Pollastrini, M., Holland, V., and Bruggemann, W. (2015) Functional traits and adaptive capacity of European forests to climate change, Environmental and Experimental Botany, vol. 111, no. 3, pp. 91 -113
Caudle, K.L., Johnson, L.C., Baer, S.G., and Maricle, B.R. (2014). A comparison of seasonal foliar chlorophyll change among ecotypes and cultivars of Andropogon gerardii (Poaceae) by using nondestructive and destructive methods, Photosynthetica, vol. 52, no. 4, pp. 511-518
El-Hajj, R., Al-Jawhazy, D., Moukaddem, T., Khater, C. (2014) Forest Sustainability in North Lebanon: A Challenging Complexity in a Changing Environment, International Journal of Forestry Research, vol. 2014, Article ID 212316, 12 pages. http://dx.doi.org/10.1155/2014/212316
Granda, V., Delatorre, C., Cuesta, C., Centeno, M.I., Fernandez, B., Rodriguez, A., Feito, I. (2014) Physiological and biochemical responses to severe drought stress of nine Eucalyptus globulus clones: a multivariate approach, Tree Physiology, vol. 34, pp. 778-786
Goth, L. (1991) A simple method for determination of serum catalase activity and revision of reference range", Clinica Chimica Acta, vol. 196, pp. 143-152
Gregory, R. P. F. (1966) A rapid assay for peroxidase activity", Bioc hemical Journal, vol. 101, no. 3, pp. 582-583
Halliwell B. (2006) Reactive species and antioxidants. Redox biology is a fundamental theme in aerobic life", Plant Physiology, vol. 141, pp. 312-322
Harfouche, A., Meilan, R., and Altman, A. ( 2014) Molecular and physiological responses to abiotic stresses in forest trees and their relevance to tree improvement, Tree Physiology, vol. 34, no. 11, pp. 1181 -1198
Mhamdi, A., Queval, G., Chaouch, S., Vanderauwera, S., Van Breusegem, F., Noctor, G. (2010) Catalase function in plants: a focus on Arabidopsis mutants as stress-mimic model", Environmental and Experimental Botany, vol. 61, no. 15, pp. 4197-4220
Mokria, M.,Gebrekirstos, A., Aynekulu, E., and Brauning, A. (2015) "Tree dieback affects climate change mitigation potential of a dry afromontane forest in northern Ethiopia", Forest Ecology and Management, vol. 344, no. 15, pp. 73-83
Parviz L.(2016) Determination of effective indices in the drought monitoring through analysis of satellite indexes. Montenegro. Agriculture and Forestry, Vol. 62. Issue 1: pp.305-324
Queval, G., Issakidis-Bourguet, E., Hoeberichts, F.A., Vandorpe, M., Gakiere, B, Vanacker, H., Miginiac-Maslow, M., Van Breusegem, F., Noctor, G. (2007) Conditional oxidative stress response in the Arabidopsis photorespiratory mutant cat2 demonstrate that redox state is a key modulator of day length-dependent gene expression, and define photoperiod as a crucial factor in the regulation of H2O2-induced cell death", The Plant Journal, vol. 52, pp. 640-657
Rajsnerova, P., Klem, K., Holub, P., Novotna, K., Vecerova, K., Kozachikova, M., Rivas-Ubach, A., Sardans, J., Marek, M.V., Penuelas, J., Urban, O. (2015) Morphological, biochemical and physiological traits of upper and lower canopy leaves European beech tends to converge with increasing altitude", Tree Physiology, vol. 35, no. 1, pp. 47 -60
Ramirez-Valiente, J.A., Koehler, K., Cavender-Bares, J. (2015) Climatic origins predict variations in photoprotective leaf pigments in response to drought and law temperature in live oaks (Quercus series virentes)", Tree Physiology, vol. 35, no. 1, pp. 521-534
Ranieri, A., Castagna, A., Baldam, B., Soldatini, G.F. (200) Iron deficiency differently affects peroxidase isoforms in sunflower", Journal of Experimental Botany, vol. 52, no. 354, pp. 25- 35
Rezende, V.L., de Miranda, P.L.S., Meyer, L., Moreira, C.V., Linhares, M.F.M, de Oliveira-Filho, A.T., Eisenlohr, P.V. (2015) Tree species composition and richness along altitudinal gradients as a tool for conservation decisions: the case of Atlantic semideciduous forest, Biodiversity Conservation, vol. 24, pp. 2149-2163
Sperlich, D., Chang, C.T., Penuelas, J., Gracia, C.., Sabate, S. (2015) Seasonal variability of foliar photosynthetic and morphological traits and drought impacts in a Mediterranean mixed forest, Tree Physiology, vol. 35, no. 5, pp. 501 -520
Talbi, S., Romero-Puertas, M.S., Hernandez, L., Terron, A., Ferchichi, A., and Sandalio, L.M. (2015) Drought tolerance in a Saharian Plant Oudneya africana: Role of antioxidant defenses", Environmental and Experimental Botany, vol. 111, no. 3, pp. 114-126
Tkach, V. P. (2012) Forests and Forest Cover in Ukraine: Current State and Prospects for Development, Ukrainian Geographical Journal, vol. 2, pp. 49 -55 (in Ukrainian).
Wintermans, J. F. G. M. & De Mots, A. (1965) Spectrophotometric Characteristics of Chlorophyll a and b and Their Phaeophytins in Etanol", Biochimica et Biophysica Acta (BBA), vol. 109, no. 2, pp. 448-453
Zadworny, M.., McCormac, M.L., Rawlik, K.., Jagodzinski, A.M. ( 2015) Seasonal variation in chemistry, but not morphology, in roots of Quercus robur growing in different soil types, Tree Physiology, vol. 35, no. 6, pp. 644 -652
Yuri LYKHOLAT, Nina KHROMYK, Irina IVAN'KO, Igor KOVALENKO, Larisa SHUPRANOVA, Mykola KHARYTONOV1
1Larisa Shupranova, (corresponding author: [email protected]), Yuri Lykholat, Nina Khromyk, Irina Ivan'ko, Oles Honchar Dnipropetrovs'k National University, Dnipropetrovsk, UKRAINE, Igor Kovalenko, Sumy' National Agricultural University, Sumy, UKRAINE, Mykola Kharytonov, Dnipropetrovsk State Agrarian and Economic University, Dnipropetrovsk, UKRAINE.
Notes: The authors declare that they have no conflicts of interest. Authorship Form signed online.
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