129 research outputs found

    Hydromorphological method and GIS tools with a web application to assess a semi-natural urbanised river

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    River valleys are an essential element of urban space, and play an important role in the functioning of the natural environment and the recreation of city dwellers. Moreover, blue-green infrastructure facilitates healthy urban living. New technologies can contribute significantly to dissemination of messages of environmental protection. We discuss adaptation of the RHS method for presenting interactive data for river channels. Our assessment was focused on three parameters: habitat area, structure and conservation. The main parameters were described using selected indicators linked to natural and anthropogenic factors. The habitat modification score showed that the physical state of the Drwinka River was obviously modified, and the habitat quality assessment rated the stream as hydromorphological class III. The web application showed that the proposed method is suitable for creating realistic visual effects, and indicates greening areas against degraded areas

    All natural habitat edges matter equally for endangered Maculinea butterflies

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    An obvious consequence of habitat fragmentation is an increasing role of habitat edges for species survival. Recently it has been suggested that the endangered butterfly Maculinea nausithous prefers forested edges of its meadow habitats. However, the prevalence of forests in the study area used for this analysis makes it impossible to distinguish whether the effect detected is a genuine preference for forest edges or a preference for any natural patch edges as opposed to patch interiors. We investigated habitat selection by Maculinea nausithous and Maculinea teleius occurring sympatrically at five habitat patches surrounded by mosaic landscape. Butterfly capture positions were marked with GPS and subsequently analysed with GIS software. Both species avoided the interiors of their patches and concentrated in the edge zone, but these preferences were visible only at three larger patches exceeding 1 ha in area. Among different types of edges those bordering densely built-up areas were avoided, whereas all natural edges (adjacent to forests, reeds or grasslands) were similarly used. We hypothesise that preferences towards natural patch edges, regardless of their type, can be explained by the spatial interactions between Maculinea butterflies and Myrmica ants they parasitise. Patch surroundings constitute refuge space for the ants, and hence their densities may be expected to be higher near patch edges. Our findings indicate the importance of patch surroundings for the persistence of Maculinea populations. Regretfully, current legal framework makes it difficult to protect patch surroundings, where neither priority species nor their habitats occur

    Calystegia sepium – an expansive weed of maize fields near Krakow

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    The aim of the present study was to assess the degree of colonization of maize fields by the greater or hedge bindweed, Calystegia sepium L. in the vicinity of Krakow, and to investigate the habitat preferences of this weed. On the basis of field trips, carried out in 88 fields of maize, we found that C. sepium had colonized approximately 30% of the fields investigated. On average, it covered 17.5% of the field area. Multivariate analyses (PCA and RDA) showed that the presence of this species was correlated with that of sandy soils as well as the proximity of streams. Analysis of the morphological features revealed that C. sepium specimens growing both in fields and in natural stands share similar morphological characteristics

    The roots of "Western European societal evolution". A concept of Europe by Jenő Szűcs

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    Jenő Szűcs wrote his essay entitled Sketch on the three regions of Europe in the early 1980s in Hungary. During these years, a historically well-argued opinion emphasising a substantial difference between Central European and Eastern European societies was warmly received in various circles of the political opposition. In a wider European perspective Szűcs used the old “liberty topos” which claims that the history of Europe is no other than the fulfillment of liberty. In his Sketch, Szűcs does not only concentrate on questions concerning the Middle Ages in Western Europe. Yet it is this stream of thought which brought a new perspective to explaining European history. His picture of the Middle Ages represents well that there is a way to integrate all typical Western motifs of post-war self-definition into a single theory. Mainly, the “liberty motif”, as a sign of “Europeanism” – in the interpretation of Bibó’s concept, Anglo-saxon Marxists and Weber’s social theory –, developed from medieval concepts of state and society and from an analysis of economic and social structures. Szűcs’s historical aspect was a typical intellectual product of the 1980s: this was the time when a few Central European historians started to outline non-Marxist aspects of social theory and categories of modernisation theories, but concealing them with Marxist terminology

    Within-patch mobility and flight morphology reflect resource use and dispersal potential in the dryad butterfly Minois dryas

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    Knowledge of mobility is essential for understanding animal habitat use and dispersal potential, especially in the case of species occurring in fragmented habitats. We compared within-patch movement distances, turning angles, resting times, and flight-related morphological traits in the locally endangered butterfly, the dryad (Minois dryas), between its old populations occupying xerothermic grasslands and newly established ones in wet meadows. We expected that the latter group should be more mobile. Individuals living in both habitat types did not differ in their body mass and size, but those from xerothermic grasslands had wider thoraxes and longer wings, thus lower wing loading index (defined as body mass to wing length ratio). The majority of movements were short and did not exceed 10 m. Movement distances were significantly larger in males. However, there was no direct effect of habitat type on movement distances. Our results suggest that the dryads from xerothermic grasslands have better flight capabilities, whereas those from wet meadows are likely to invest more in reproduction. This implies that mobility is shaped by resource availability rather than by recent evolutionary history. Lower female mobility may have negative implications for the metapopulation persistence because only mated females are able to (re)colonise vacant habitat patches efficiently. Conservation efforts should thus be focused on maintaining large habitat patches that prevent stochastic local extinctions. Furthermore, the recommendation of promoting the exchange of individuals among patches through improving matrix permeability, as well as assisted reintroductions of the species into suitable vacant habitats should also improve its conservation

    Identification of salt and drought biochemical stress markers in several Silene vulgaris populations

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    [EN] This study attempted to determine short-term responses to drought and salt stress in different Silene vulgaris genotypes and to identify potential abiotic stress biochemical indicators in this species. Four populations from contrasting habitats were subjected to drought and three levels of salinity under controlled greenhouse conditions. The determination of several growth parameters after the stress treatments allowed for ranking the tolerance to stress of the four analyzed populations on the basis of their relative degree of stress-induced growth inhibition. This was then correlated with changes in the leaf levels of monovalent ions (Na+, Cl-, and K+), photosynthetic pigments (chlorophylls a and b, carotenoids), osmolytes (total soluble sugars, proline), and non-enzymatic antioxidants (total phenolic compounds and flavonoids). Despite the observed differences, all four populations appeared to be relatively tolerant to both stress conditions, which in general did not cause a significant degradation of photosynthetic pigments and did not generate oxidative stress in the plants. Drought and salinity tolerance in S. vulgaris was mostly dependent on the use of Na+ and K+ for osmotic adjustment under stress, a mechanism that appeared to be constitutive, and not stress-induced, since relatively high concentrations of these cations (without reaching toxic levels) were also present in the leaves of control plants. The inhibition of additional transportation of toxic ions to the leaves, in response to increasing external salinity, seemed to be a relevant mechanism of tolerance, specifically to salt stress, whereas accumulation of soluble sugars under drought conditions may have contributed to tolerance to drought.This research was supported in part by the Ministry of Science and Higher Education of the Republic of Poland as DS 3500/ZBiFR-IBRiB-WBiO-UR and the Erasmus+ Program granted for Aleksandra Kozminska to complete her doctoral studies.Kozminska, A.; Wiszniewska, A.; Hanus-Fajerska, E.; Boscaiu, M.; Al Hassan, M.; Halecki, W.; Vicente, O. (2019). Identification of salt and drought biochemical stress markers in several Silene vulgaris populations. Sustainability. 11(3):1-23. https://doi.org/10.3390/su11030800123113Grime, J. P. (1977). Evidence for the Existence of Three Primary Strategies in Plants and Its Relevance to Ecological and Evolutionary Theory. The American Naturalist, 111(982), 1169-1194. doi:10.1086/283244Bartels, D., & Sunkar, R. (2005). Drought and Salt Tolerance in Plants. Critical Reviews in Plant Sciences, 24(1), 23-58. doi:10.1080/07352680590910410Rengasamy, P. (2010). Soil processes affecting crop production in salt-affected soils. Functional Plant Biology, 37(7), 613. doi:10.1071/fp09249Rahman, M. M., Hagare, D., Maheshwari, B., & Dillon, P. (2015). Impacts of Prolonged Drought on Salt Accumulation in the Root Zone Due to Recycled Water Irrigation. Water, Air, & Soil Pollution, 226(4). doi:10.1007/s11270-015-2370-1Martínez-Fernández, J., González-Zamora, A., Sánchez, N., Gumuzzio, A., & Herrero-Jiménez, C. M. (2016). Satellite soil moisture for agricultural drought monitoring: Assessment of the SMOS derived Soil Water Deficit Index. Remote Sensing of Environment, 177, 277-286. doi:10.1016/j.rse.2016.02.064Laiskhanov, S., Otarov, A., Savin, I., Tanirbergenov, S., Mamutov, Z., Duisekov, S., & Zhogolev, A. (2016). Dynamics of Soil Salinity in Irrigation Areas in South Kazakhstan. Polish Journal of Environmental Studies, 25(6), 2469-2475. doi:10.15244/pjoes/61629López-Jurado, J., Balao, F., & Mateos-Naranjo, E. (2016). Deciphering the ecophysiological traits involved during water stress acclimation and recovery of the threatened wild carnation, Dianthus inoxianus. Plant Physiology and Biochemistry, 109, 397-405. doi:10.1016/j.plaphy.2016.10.023Lopez, J. R., Winter, J. M., Elliott, J., Ruane, A. C., Porter, C., & Hoogenboom, G. (2017). Integrating growth stage deficit irrigation into a process based crop model. Agricultural and Forest Meteorology, 243, 84-92. doi:10.1016/j.agrformet.2017.05.001Yeh, C.-H., Kaplinsky, N. J., Hu, C., & Charng, Y. (2012). Some like it hot, some like it warm: Phenotyping to explore thermotolerance diversity. Plant Science, 195, 10-23. doi:10.1016/j.plantsci.2012.06.004Zaher-Ara, T., Boroomand, N., & Sadat-Hosseini, M. (2016). Physiological and morphological response to drought stress in seedlings of ten citrus. Trees, 30(3), 985-993. doi:10.1007/s00468-016-1372-yNxele, X., Klein, A., & Ndimba, B. K. (2017). Drought and salinity stress alters ROS accumulation, water retention, and osmolyte content in sorghum plants. South African Journal of Botany, 108, 261-266. doi:10.1016/j.sajb.2016.11.003Ohama, N., Sato, H., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2017). Transcriptional Regulatory Network of Plant Heat Stress Response. Trends in Plant Science, 22(1), 53-65. doi:10.1016/j.tplants.2016.08.015Ashraf, M. (2010). Inducing drought tolerance in plants: Recent advances. Biotechnology Advances, 28(1), 169-183. doi:10.1016/j.biotechadv.2009.11.005Fita, A., Rodríguez-Burruezo, A., Boscaiu, M., Prohens, J., & Vicente, O. (2015). Breeding and Domesticating Crops Adapted to Drought and Salinity: A New Paradigm for Increasing Food Production. Frontiers in Plant Science, 6. doi:10.3389/fpls.2015.00978Gorim, L. Y., & Vandenberg, A. (2017). Evaluation of Wild Lentil Species as Genetic Resources to Improve Drought Tolerance in Cultivated Lentil. Frontiers in Plant Science, 8. doi:10.3389/fpls.2017.01129Ariga, H., Katori, T., Yoshihara, R., Hase, Y., Nozawa, S., Narumi, I., … Taji, T. (2013). Arabidopsissos1 mutant in a salt-tolerant accession revealed an importance of salt acclimation ability in plant salt tolerance. Plant Signaling & Behavior, 8(7), e24779. doi:10.4161/psb.24779Ben Rejeb, K., Lefebvre-De Vos, D., Le Disquet, I., Leprince, A.-S., Bordenave, M., Maldiney, R., … Savouré, A. (2015). Hydrogen peroxide produced by NADPH oxidases increases proline accumulation during salt or mannitol stress inArabidopsis thaliana. New Phytologist, 208(4), 1138-1148. doi:10.1111/nph.13550Kumar, D., Al Hassan, M., Naranjo, M. A., Agrawal, V., Boscaiu, M., & Vicente, O. (2017). Effects of salinity and drought on growth, ionic relations, compatible solutes and activation of antioxidant systems in oleander (Nerium oleander L.). PLOS ONE, 12(9), e0185017. doi:10.1371/journal.pone.0185017Al Hassan, M., Morosan, M., López-Gresa, M., Prohens, J., Vicente, O., & Boscaiu, M. (2016). Salinity-Induced Variation in Biochemical Markers Provides Insight into the Mechanisms of Salt Tolerance in Common (Phaseolus vulgaris) and Runner (P. coccineus) Beans. International Journal of Molecular Sciences, 17(9), 1582. doi:10.3390/ijms17091582Alarcón, R., Ortiz, L. T., & García, P. (2006). Nutrient and fatty acid composition of wild edible bladder campion populations [Silene vulgaris (Moench.) Garcke]. International Journal of Food Science and Technology, 41(10), 1239-1242. doi:10.1111/j.1365-2621.2006.01187.xCeccanti, C., Landi, M., Benvenuti, S., Pardossi, A., & Guidi, L. (2018). Mediterranean Wild Edible Plants: Weeds or «New Functional Crops»? Molecules, 23(9), 2299. doi:10.3390/molecules23092299Boari, F., Cefola, M., Di Gioia, F., Pace, B., Serio, F., & Cantore, V. (2013). Effect of cooking methods on antioxidant activity and nitrate content of selected wild Mediterranean plants. International Journal of Food Sciences and Nutrition, 64(7), 870-876. doi:10.3109/09637486.2013.799125Disciglio, G., Tarantino, A., Frabboni, L., Gagliardi, A., Giuliani, M. M., Tarantino, E., & Gatta, G. (2017). Qualitative characterization of cultivated and wild edible plants: mineral elements, phenols content and antioxidant capacity. Italian Journal of Agronomy, 11. doi:10.4081/ija.2017.1036Bhatt, J., Kumar, S., Patel, S., & Solanki, R. (2017). Sequence-related amplified polymorphism (SRAP) markers based genetic diversity analysis of cumin genotypes. Annals of Agrarian Science, 15(4), 434-438. doi:10.1016/j.aasci.2017.09.001Sebasky, M. E., Keller, S. R., & Taylor, D. R. (2016). Investigating past range dynamics for a weed of cultivation, Silene vulgaris. Ecology and Evolution, 6(14), 4800-4811. doi:10.1002/ece3.2250Schiop, S. T., Al Hassan, M., Sestras, A. F., Boscaiu, M., Sestras, R. E., & Vicente, O. (2015). Identification of Salt Stress Biomarkers in Romanian Carpathian Populations of Picea abies (L.) Karst. PLOS ONE, 10(8), e0135419. doi:10.1371/journal.pone.0135419BRATTELER, M., LEXER, C., & WIDMER, A. (2006). Genetic architecture of traits associated with serpentine adaptation of Silene vulgaris. Journal of Evolutionary Biology, 19(4), 1149-1156. doi:10.1111/j.1420-9101.2006.01090.xSandner, T. M., & Matthies, D. (2017). Fluctuating asymmetry of leaves is a poor indicator of environmental stress and genetic stress by inbreeding in Silene vulgaris. Ecological Indicators, 79, 247-253. doi:10.1016/j.ecolind.2017.04.030Wierzbicka, M., & Panufnik, D. (1998). The adaptation of Silene vulgaris to growth on a calamine waste heap (S. Poland). Environmental Pollution, 101(3), 415-426. doi:10.1016/s0269-7491(98)00012-8VERKLEIJ, J. A. C., & PRAST, J. E. (1989). Cadmium tolerance and co-tolerance in Silene vulgaris (Moench.) Garcke [= S. cucubalus (L.) Wib.]. New Phytologist, 111(4), 637-645. doi:10.1111/j.1469-8137.1989.tb02358.xHanus-Fajerska, E., Czura, A., Grabski, K., & Tukaj, Z. (2009). The effect of conditioned medium obtained from Scenedesmus subspicatus on suspension culture of Silene vulgaris (Caryophyllaceae). Acta Physiologiae Plantarum, 31(5), 881-887. doi:10.1007/s11738-009-0301-8Ernst, W. H. ., & Nelissen, H. J. . (2000). Life-cycle phases of a zinc- and cadmium-resistant ecotype of Silene vulgaris in risk assessment of polymetallic mine soils. Environmental Pollution, 107(3), 329-338. doi:10.1016/s0269-7491(99)00174-8Baloun, J., Nevrtalova, E., Kovacova, V., Hudzieczek, V., Cegan, R., Vyskot, B., & Hobza, R. (2014). Characterization of the HMA7 gene and transcriptomic analysis of candidate genes for copper tolerance in two Silene vulgaris ecotypes. Journal of Plant Physiology, 171(13), 1188-1196. doi:10.1016/j.jplph.2014.04.014Pradas-del-Real, A. E., García-Gonzalo, P., Alarcón, R., González-Rodríguez, A., Lobo, M. C., & Pérez-Sanz, A. (2013). Effect of genotype, Cr(III) and Cr(VI) on plant growth and micronutrient status in Silene vulgaris (Moench). Spanish Journal of Agricultural Research, 11(3), 685. doi:10.5424/sjar/2013113-3536Pradas del Real, A. E., García-Gonzalo, P., Lobo, M. C., & Pérez-Sanz, A. (2014). Chromium speciation modifies root exudation in two genotypes of Silene vulgaris. Environmental and Experimental Botany, 107, 1-6. doi:10.1016/j.envexpbot.2014.05.002García-Gonzalo, P., del Real, A. E. P., Lobo, M. C., & Pérez-Sanz, A. (2016). Different genotypes of Silene vulgaris (Moench) Garcke grown on chromium-contaminated soils influence root organic acid composition and rhizosphere bacterial communities. Environmental Science and Pollution Research, 24(33), 25713-25724. doi:10.1007/s11356-016-6667-4Baker, A. J. M., Brooks, R. R., Pease, A. J., & Malaisse, F. (1983). Studies on copper and cobalt tolerance in three closely related taxa within the genusSilene L. (Caryophyllaceae) from Zaïre. Plant and Soil, 73(3), 377-385. doi:10.1007/bf02184314Gonnelli, C., Galardi, F., & Gabbrielli, R. (2001). Nickel and copper tolerance and toxicity in three Tuscan populations of Silene paradoxa. Physiologia Plantarum, 113(4), 507-514. doi:10.1034/j.1399-3054.2001.1130409.xPALIOURIS, G., & HUTCHINSON, T. C. (1991). Arsenic, cobalt and nickel tolerances in two populations of Silene vulgaris (Moench) Garcke from Ontario, Canada. New Phytologist, 117(3), 449-459. doi:10.1111/j.1469-8137.1991.tb00009.xKrämer, U. (2018). Conceptualizing plant systems evolution. Current Opinion in Plant Biology, 42, 66-75. doi:10.1016/j.pbi.2018.02.008Kozminska, A., Al Hassan, M., Hanus-Fajerska, E., Naranjo, M. A., Boscaiu, M., & Vicente, O. (2018). Comparative analysis of water deficit and salt tolerance mechanisms in Silene. South African Journal of Botany, 117, 193-206. doi:10.1016/j.sajb.2018.05.022Weimberg, R. (1987). Solute adjustments in leaves of two species of wheat at two different stages of growth in response to salinity. Physiologia Plantarum, 70(3), 381-388. doi:10.1111/j.1399-3054.1987.tb02832.xLICHTENTHALER, H. K., & WELLBURN, A. R. (1983). Determinations of total carotenoids and chlorophylls a and b of leaf extracts in different solvents. Biochemical Society Transactions, 11(5), 591-592. doi:10.1042/bst0110591Hodges, D. M., DeLong, J. M., Forney, C. F., & Prange, R. K. (1999). Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta, 207(4), 604-611. doi:10.1007/s004250050524Gil, R., Bautista, I., Boscaiu, M., Lidon, A., Wankhade, S., Sanchez, H., … Vicente, O. (2014). Responses of five Mediterranean halophytes to seasonal changes in environmental conditions. AoB PLANTS, 6(0), plu049-plu049. doi:10.1093/aobpla/plu049Blainski, A., Lopes, G., & de Mello, J. (2013). Application and Analysis of the Folin Ciocalteu Method for the Determination of the Total Phenolic Content from Limonium Brasiliense L. Molecules, 18(6), 6852-6865. doi:10.3390/molecules18066852Zhishen, J., Mengcheng, T., & Jianming, W. (1999). The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals. Food Chemistry, 64(4), 555-559. doi:10.1016/s0308-8146(98)00102-2Bates, L. S., Waldren, R. P., & Teare, I. D. (1973). Rapid determination of free proline for water-stress studies. Plant and Soil, 39(1), 205-207. doi:10.1007/bf00018060DuBois, M., Gilles, K. A., Hamilton, J. K., Rebers, P. A., & Smith, F. (1956). Colorimetric Method for Determination of Sugars and Related Substances. Analytical Chemistry, 28(3), 350-356. doi:10.1021/ac60111a017Flowers, T. J., & Colmer, T. D. (2008). Salinity tolerance in halophytes*. New Phytologist, 179(4), 945-963. doi:10.1111/j.1469-8137.2008.02531.xGupta, B., & Huang, B. (2014). Mechanism of Salinity Tolerance in Plants: Physiological, Biochemical, and Molecular Characterization. International Journal of Genomics, 2014, 1-18. doi:10.1155/2014/701596Nardini, A., Lo Gullo, M. A., Trifilò, P., & Salleo, S. (2014). The challenge of the Mediterranean climate to plant hydraulics: Responses and adaptations. Environmental and Experimental Botany, 103, 68-79. doi:10.1016/j.envexpbot.2013.09.018Yang, L., Fountain, J., Wang, H., Ni, X., Ji, P., Lee, R., … Guo, B. (2015). Stress Sensitivity Is Associated with Differential Accumulation of Reactive Oxygen and Nitrogen Species in Maize Genotypes with Contrasting Levels of Drought Tolerance. International Journal of Molecular Sciences, 16(10), 24791-24819. doi:10.3390/ijms161024791Ouyang, B., Yang, T., Li, H., Zhang, L., Zhang, Y., Zhang, J., … Ye, Z. (2007). Identification of early salt stress response genes in tomato root by suppression subtractive hybridization and microarray analysis. Journal of Experimental Botany, 58(3), 507-520. doi:10.1093/jxb/erl258Beritognolo, I., Harfouche, A., Brilli, F., Prosperini, G., Gaudet, M., Brosche, M., … Sabatti, M. (2011). Comparative study of transcriptional and physiological responses to salinity stress in two contrasting Populus alba L. genotypes. Tree Physiology, 31(12), 1335-1355. doi:10.1093/treephys/tpr083Ma, H., Song, L., Shu, Y., Wang, S., Niu, J., Wang, Z., … Ma, H. (2012). Comparative proteomic analysis of seedling leaves of different salt tolerant soybean genotypes. Journal of Proteomics, 75(5), 1529-1546. doi:10.1016/j.jprot.2011.11.026Cui, D., Wu, D., Liu, J., Li, D., Xu, C., Li, S., … Zhao, L. (2015). Proteomic Analysis of Seedling Roots of Two Maize Inbred Lines That Differ Significantly in the Salt Stress Response. PLOS ONE, 10(2), e0116697. doi:10.1371/journal.pone.0116697Widodo, Patterson, J. H., Newbigin, E., Tester, M., Bacic, A., & Roessner, U. (2009). Metabolic responses to salt stress of barley (Hordeum vulgare L.) cultivars, Sahara and Clipper, which differ in salinity tolerance. Journal of Experimental Botany, 60(14), 4089-4103. doi:10.1093/jxb/erp243Zhao, X., Wang, W., Zhang, F., Deng, J., Li, Z., & Fu, B. (2014). Comparative Metabolite Profiling of Two Rice Genotypes with Contrasting Salt Stress Tolerance at the Seedling Stage. PLoS ONE, 9(9), e108020. doi:10.1371/journal.pone.0108020Zhu, J.-K. (2001). Plant salt tolerance. Trends in Plant Science, 6(2), 66-71. doi:10.1016/s1360-1385(00)01838-0Grossi, D., Rustioni, L., Simone Di Lorenzo, G., Failla, O., & Brancadoro, L. (2016). Water deficit effects on grapevine woody tissue pigmentations. Horticultural Science, 43(No. 4), 188-194. doi:10.17221/186/2015-hortsciRajakaruna, N. (2017). Lessons on Evolution from the Study of Edaphic Specialization. The Botanical Review, 84(1), 39-78. doi:10.1007/s12229-017-9193-2Vasseur, F., Bresson, J., Wang, G., Schwab, R., & Weigel, D. (2018). Image-based methods for phenotyping growth dynamics and fitness components in Arabidopsis thaliana. Plant Methods, 14(1). doi:10.1186/s13007-018-0331-6Andrade, E. R., Ribeiro, V. N., Azevedo, C. V. G., Chiorato, A. F., Williams, T. C. R., & Carbonell, S. A. M. (2016). Biochemical indicators of drought tolerance in the common bean (Phaseolus vulgaris L.). Euphytica, 210(2), 277-289. doi:10.1007/s10681-016-1720-4Bacha, H., Tekaya, M., Drine, S., Guasmi, F., Touil, L., Enneb, H., … Ferchichi, A. (2017). Impact of salt stress on morpho-physiological and biochemical parameters of Solanum lycopersicum cv. Microtom leaves. South African Journal of Botany, 108, 364-369. doi:10.1016/j.sajb.2016.08.018Sen, A., Ozturk, I., Yaycili, O., & Alikamanoglu, S. (2017). Drought Tolerance in Irradiated Wheat Mutants Studied by Genetic and Biochemical Markers. Journal of Plant Growth Regulation, 36(3), 669-679. doi:10.1007/s00344-017-9668-8Horie, T., Karahara, I., & Katsuhara, M. (2012). Salinity tolerance mechanisms in glycophytes: An overview with the central focus on rice plants. Rice, 5(1). doi:10.1186/1939-8433-5-11Baetz, U., Eisenach, C., Tohge, T., Martinoia, E., & De Angeli, A. (2016). Vacuolar Chloride Fluxes Impact Ion content and Distribution during Early Salinity Stress. Plant Physiology, pp.00183.2016. doi:10.1104/pp.16.00183Assaha, D. V. M., Ueda, A., Saneoka, H., Al-Yahyai, R., & Yaish, M. W. (2017). The Role of Na+ and K+ Transporters in Salt Stress Adaptation in Glycophytes. Frontiers in Physiology, 8. doi:10.3389/fphys.2017.00509Wu, H. (2018). Plant salt tolerance and Na+ sensing and transport. The Crop Journal, 6(3), 215-225. doi:10.1016/j.cj.2018.01.003CRAIG PLETT, D., & MØLLER, I. S. (2010). Na+transport in glycophytic plants: what we know and would like to know. Plant, Cell & Environment, 33(4), 612-626. doi:10.1111/j.1365-3040.2009.02086.xFlowers, T. J., Troke, P. F., & Yeo, A. R. (1977). The Mechanism of Salt Tolerance in Halophytes. Annual Review of Plant Physiology, 28(1), 89-121. doi:10.1146/annurev.pp.28.060177.000513Genc, Y., Oldach, K., Taylor, J., & Lyons, G. H. (2015). Uncoupling of sodium and chloride to assist breeding for salinity tolerance in crops. New Phytologist, 210(1), 145-156. doi:10.1111/nph.13757Greenway, H., & Munns, R. (1980). Mechanisms of Salt Tolerance in Nonhalophytes. Annual Review of Plant Physiology, 31(1), 149-190. doi:10.1146/annurev.pp.31.060180.001053Hänsch, R., & Mendel, R. R. (2009). Physiological functions of mineral micronutrients (Cu, Zn, Mn, Fe, Ni, Mo, B, Cl). Current Opinion in Plant Biology, 12(3), 259-266. doi:10.1016/j.pbi.2009.05.006Maathuis, F. J. (2009). Physiological functions of mineral macronutrients. Current Opinion in Plant Biology, 12(3), 250-258. doi:10.1016/j.pbi.2009.04.003Moinuddin, & Imas, P. (2014). Potassium Uptake in Relation to Drought Tolerance of Chickpea Under Rain-Fed Conditions. Journal of Plant Nutrition, 37(7), 1120-1138. doi:10.1080/01904167.2014.881863Zhang, X., Wu, H., Chen, L., Liu, L., & Wan, X. (2018). Maintenance of mesophyll potassium and regulation of plasma membrane H+-ATPase are associated with physiological responses of tea plants to drought and subsequent rehydration. The Crop Journal, 6(6), 611-620. doi:10.1016/j.cj.2018.06.001Wang, M., Zheng, Q., Shen, Q., & Guo, S. (2013). The Critical Role of Potassium in Plant Stress Response. International Journal of Molecular Sciences, 14(4), 7370-7390. doi:10.3390/ijms14047370Al Hassan, M., Chaura, J., Donat-Torres, M. P., Boscaiu, M., & Vicente, O. (2017). Antioxidant responses under salinity and drought in three closely related wild monocots with different ecological optima. AoB PLANTS, 9(2). doi:10.1093/aobpla/plx009Koźmińska, A., Al Hassan, M., Wiszniewska, A., Hanus-Fajerska, E., Boscaiu, M., & Vicente, O. (2019). Responses of succulents to drought: Comparative analysis of four Sedum (Crassulaceae) species. Scientia Horticulturae, 243, 235-242. doi:10.1016/j.scienta.2018.08.028Nikolaeva, M. K., Maevskaya, S. N., Shugaev, A. G., & Bukhov, N. G. (2010). Effect of drought on chlorophyll content and antioxidant enzyme activities in leaves of three wheat cultivars varying in productivity. Russian Journal of Plant Physiology, 57(1), 87-95. doi:10.1134/s1021443710010127Del Rio, D., Stewart, A. J., & Pellegrini, N. (2005). A review of recent studies on malondialdehyde as toxic molecule and biological marker of oxidative stress. Nutrition, Metabolism and Cardiovascular Diseases, 15(4), 316-328. doi:10.1016/j.numecd.2005.05.003Cheynier, V., Comte, G., Davies, K. M., Lattanzio, V., & Martens, S. (2013). Plant phenolics: Recent advances on their biosynthesis, genetics, and ecophysiology. Plant Physiology and Biochemistry, 72, 1-20

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