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2019 | 41 | 06 |
Tytuł artykułu

Physio-morphological traits and drought stress responses in three wild Mediterranean taxa of Brassicaceae

Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Crop wild relatives (CWRs) have extremely relevant roles in biodiversity conservation, in investigating phylogeny and improving abiotic stress tolerance of crop plants. We screened the variability in leaf functional traits of three CWRs of kale crops (Brassica oleracea) from Sicily, Italy, grown in pots under well-watered and drought conditions. Our aim was to highlight traits in the different genotypes of endemic Sicilian threatened taxa. We measured several structural/anatomical traits (stomatal size, density and stomatal pore index—SPI, leaf mass per area—LMA) and leaf functional traits (stomatal conductance—gs, leaf water potential—ΨL, leaf temperature (TL), leaf relative water content—RWC) at pre-dawn and midday of leaves of three wild taxa: B. macrocarpa, B. rupestris subsp. rupestris and B. villosa subsp. bivoniana. Pressure–volume curves were constructed to obtain leaf water potential at turgor loss point (Ψtlp), osmotic potential at full rehydration (Ψπ100), relative water content at turgor loss point (RWCtlp), elastic bulk modulus (εmax) and leaf area specific capacitance at full turgor (Cft*). Several significant differences were found among the taxa: under water deficit, B. macrocarpa had the less negative Ψtlp and showed the smallest ΔΨL between pre-dawn and midday. B. villosa subsp. bivoniana showed the highest SPI and had significantly higher gs under water availability, while under drought it had the most negative ΨL. Each of the taxa investigated possessed traits that confer particular stress tolerance, offer competitive advantage in their natural environment and may be exploited for crop improvement.
Słowa kluczowe
Wydawca
-
Rocznik
Tom
41
Numer
06
Opis fizyczny
Article 106 [11p.], fig.,ref.
Twórcy
autor
  • Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, via Archirafi 38, 90123 Palermo, Italy
autor
  • Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, via Archirafi 38, 90123 Palermo, Italy
autor
  • Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, via Archirafi 38, 90123 Palermo, Italy
Bibliografia
  • Abrams MD, Kubiske ME (1990) Leaf structural characteristics of 31 hardwood and conifer tree species in central Wisconsin: influence of light regime and shade-tolerance rank. For Ecol Manag 31:245–253
  • Ashraf M, Sharif R (1997) Does salt tolerance vary in a potential oil seed crop Brassica carinata at different growth stages? J Agron Crop Sci 181:103–115
  • Baker RL, Yarkhunova Y, Vidal K, Ewers BE, Weinig C (2017) Polyploidy and the relationship between leaf structure and function: implications for correlated evolution of anatomy, morphology, and physiology in Brassica. BMC Plant Biol 17:3. https://doi.org/10.1186/s12870-016-0957-3
  • Bartlett MK, Scoffoni C, Sack L (2012) The determinants of leaf turgor loss point and prediction of drought tolerance of species and biomes: a global meta-analysis. Ecol Lett 15:393–405
  • Bartlett MK, Zhang Y, Kreidler N, Sun S, Ardy R, Cao K, Sack L (2014) Global analysis of plasticity in turgor loss point, a key drought tolerance trait. Ecol Lett 17:1580–1590
  • Beltrao J, Faria J, Miguel G, Chaves P, Trindade D (2000) Cabbage yield response to salinity of trickle irrigation water. Acta Hortic 537:641–645
  • Biemond H, Vos J, Struik PC (1995) Effects of nitrogen on accumulation and partitioning of dry matter and nitrogen of vegetables. 1 Brussels sprouts. Neth J Agr Sci 43:419–433
  • Blum A (2017) Osmotic adjustment is a prime drought stress adaptive engine in support of plant production. Plant Cell Environ 40:4–10
  • Branca F, Cartea E (2011) Brassica. In: Kole C (ed) Wild crop relatives: genomic and breeding resources. Springer Oilseeds, Dordrecht, pp 17–36
  • Branca F, Donnini D (2013) Brassica rupestris. The IUCN red list of threatened species 2013:e.T170114A6719025. https://doi.org/10.2305.
  • Branca F, Tribulato A (2013) Brassica macrocarpa. The IUCN red list of threatened species 2013:e.T162139A5548195. https://doi.org/10.2305/IUCN.UK.2011-1.RLTS.T162139A5548195.en
  • Branca F, Argento S, Tribulato A 2012 Assessing genetic reserves in Sicily (Italy): the Brassica wild relatives case study. In: Maxted N, Dulloo ME, Ford-Lloyd BV, Frese L, Iriondo JM, Pinheiro de Carvalho MAA (eds) Agrobiodiversity conservation: securing the diversity of crop wild relatives and landraces, CABI, Wallingford, pp 52–58.
  • Bussotti F, Pollastrini M, Holland V, Brüggemann W (2015) Functional traits and adaptive capacity of European forests to climate change. Environ Exp Bot 111:91–113
  • Cirelli D, Equiza MA, Lieffers VJ, Tyree MT (2016) Populus species from diverse habitats maintain high night-time conductance under drought. Tree Physiol 36:229–242
  • Conti F, Manzi A, Pedrotti F (1997) Liste Rosse Regionali delle Piante d’Italia. Associazione Italiana per il World Wildlife Fund & Società’ Botanica Italiana, Camerino
  • Crescente M, Gratani L (2013) Differences in morphological, physiological and growth traits between two endemic subspecies of Brassica rupestris Raf.: implications for their conservation. Am J Plant Sci 4:42–50
  • Donovan LA, Linton MJ, Richars JH (2001) Predawn plant water potential does not necessarily equilibrate with soil water potential under well-watered conditions. Oecologia 129:325–328
  • Edwards CE, Ewers BE, Williams DG, Xie Q, Lou P, Xu X, McClung CR, Weinig C (2011) The genetic architecture of ecophysiological and circadian traits in Brassica rapa. Genetics 189:375–390
  • Esquinas-Alcázar JT (2005) Protecting crop genetic diversity for food security: political, ethical and technical challenges. Nat Rev Genet 6:946–953
  • Farrell C, Christopher S, Arndt SK (2017) Does the turgor loss point characterize drought response in dryland plants? Plant Cell Environ 40:1500–1511
  • Faulkner K, Mithen R, Williamson G (1998) Selective increase of the potential anticarcinogen 4-methylsulphinylbutyl glucosinolate in broccoli. Carcinogenesis 19(4):605–609
  • Feller U (2016) Drought stress and carbon assimilation in a warming climate: reversible and irreversible impacts. J Plant Physiol 203:84–94
  • Fita 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. Front Plant Sci 6:978. https://doi.org/10.3389/fpls.2015.00978
  • Francois LE (1994) Growth, seed yield and oil content of canola grown under saline conditions. Agron J 86:233–237
  • Gepts P (2004) Crop domestication as a long-term selection experiment. Plant Breed Rev 24:1–44
  • Geraci A, P Mazzola (2012) Brassica macrocarpa Guss. In: Rossi G, Foggi B, Gennai M, Gargano D, Montagnani C, Orsenigo S, Pedrini S (eds) Schede per una Lista Rossa della Flora vascolare e crittogamica Italiana. Italian Botanist 44(2):417–420.
  • Geraci A, Divaret I, Raimondo FM, Chèvre AM (2001) Genetic relationships between Sicilian wild populations of Brassica analysed with RAPD markers. Plant Breed 120:193–196
  • Geraci A, Chèvre AM, Divaret I, Eber F, Raimondo FM (2004) Isozyme analysis of genetic diversity in wild Sicilian populations of Brassica sect. Brassica in view of genetic resources management. Genet Resour Crop Ev 51:137–146
  • Greenwood S, Ruiz-Benito P, Martínez-Vilalta J, Lloret F, Kitzberger T, Allen CD, Fensham R, Laughlin DC, Kattge J, Bönisch G, Kraft NJB, Jump AS (2017) Tree mortality across biomes is promoted by drought intensity, lower wood density and higher specific leaf area. Ecol Lett 20:539–553
  • Hammer K (1984) Das Domestikationssyndrom. Kulturpflanze 32:11–34
  • Hayat S, Ali B, Hasan SA, Ahmad A (2007) Effect of 28-homobrassinolide on salinity-induced changes in Brassica juncea. Turk J Biol 31:141–146
  • Heschel MS, Dalton K, Jamason M, D’Agnese A, Ruane LG (2017) Drought response strategies of Clarkia gracilis (Onagraceae) populations from serpentine and nonserpentine soils. Int J Plant Sci 178:313–319
  • Holmes MG, Keiller DR (2002) Effects of pubescence and waxes on the reflectance of leaves in the ultraviolet and photosynthetic wavebands: a comparison of a range of species. Plant Cell Environ 25:85–93
  • Hopkins JJ, Maxted N (2010) Crop wild relatives: plant conservation for food security. Natural England Research Reports 037. Natural England, Sheffield.
  • Jullien A, Allirand JM, Mathieu A, Andrieu B, Ney B (2009) Variations in leaf mass per area according to N nutrition, plant age, and leaf position reflect ontogenetic plasticity in winter oilseed rape (Brassica napus L.). Field Crop Res 114:188–197
  • Kangur O, Kupper P, Sellin A (2017) Predawn disequilibrium between soil and plant water potentials in light of climate trends predicted for northern Europe. Reg Environ Change 17:2159–2168
  • Kattge S, Díaz S, Lavorel IC, Prentice P, Leadley G, Bönisch E, Garnier M, Westoby PB, Reich IJ, Wright JH et al (2011) TRY—a global database of plant traits. Global Change Biol 17:2905–2935
  • Kole C (2011) Wild crop relatives: genomic and breeding resources. Oilseeds Springer, Berlin Heidelberg
  • Laila R, Robin AHK, Yang K, Park JI, Suh MC, Kim J, Nou IS (2017) Developmental and genotypic variation in leaf wax content and composition, and in expression of wax biosynthetic genes in Brassica oleracea var. capitata. Front Plant Sci 7:1972. https://doi.org/10.3389/fpls.2016.01972
  • Li B, Suzuki JI, Hara T (1999) Competitive ability of two Brassica varieties in relation to biomass allocation and morphological plasticity under varying nutrient availability. Ecol Res 14:255–266
  • Ma Q, Turner DW (2006) Osmotic adjustment segregates with and is positively related to seed yield in F3 lines of crosses between Brassica napus and B. juncea subjected to water deficit. Anim Prod Sci 46:1621–1627
  • Ma Q, Niknam SR, Turner DW (2006) Responses of osmotic adjustment and seed yield of Brassica napus and B. juncea to soil water deficit at different growth stages. Crop Pasture Sci 57:221–226
  • Maggio A, De Pascale S, Ruggiero C, Barbieri G (2005) Physiological response of field-grown cabbage to salinity and drought stress. Eur J Agron 23:57–67
  • Mart KB, Veneklaas EJ, Ramley HEB (2016) Osmotic potential at full turgor: an easily measurable trait to help breeders select for drought tolerance in wheat. Plant Breed 135:279–285
  • Mithen R, Faulkner K, Magrath R, Rose P, Willianson G, Marquez L (2003) Development of isothiociante-enriched broccoli and its enhanced ability to induce phase 2 detoxification in mammalian cells. Theor Appl Genet 106:727–734
  • Munné-Bosch S, Peñuelas J (2004) Drought-induced oxidative stress in strawberry tree (Arbutus unedo L.) growing in Mediterranean field conditions. Plant Sci 166(4):1105–1110
  • Nardini A, Casolo V, Dal Borgo A, Savi T, Stenni B, Bertoncin P, Zini L, McDowell NG (2016) Rooting depth, water relations and non-structural carbohydrate dynamics in three woody angiosperms differentially affected by an extreme summer drought. Plant Cell Environ 39:618–627
  • Niknam SR, Ma Q, Turner DW (2003) Osmotic adjustment and seed yield of Brassica napus and B. juncea genotypes in a water-limited environment in south-western Australia. Anim Prod Sci 43:1127–1135
  • Norouzi M, Toorchi M, Salekdeh GH, Mohammadi SA, Neyshabouri MR, Aharizad S (2008) Effect of water deficit on growth, grain yield and osmotic adjustment in rapeseed. J Food Agric Environ 6:312–318
  • O'Brien MJ, Engelbrecht BMJ, Joswig J, Pereyra G, Schuldt B, Jansen S, Kattge J, Landhäusser SM, Levick SR, Preisler Y, Väänänen P, Macinnis-Ng C (2017) A synthesis of tree functional traits related to drought-induced mortality in forests across climatic zones. J Appl Ecol 54(6):1669–1686. https://doi.org/10.1111/1365-2664.12874
  • Oddo E, Inzerillo S, La Bella F, Grisafi F, Salleo S, Nardini A (2011) Short-term effects of potassium fertilization on the hydraulic conductance of Laurus nobilis L. Tree Physiol 31:131–138
  • Palmer AR, Fuentes S, Taylor D, Macinnis-Ng C, Zeppel M, Yunusa I, February E, Eamus D (2008) The use of pre-dawn leaf water potential and MODIS LAI to explore seasonal trends in the phenology of Australian and southern African woodlands and savannas. Aust J Bot 56:557–563
  • Pearce DW, Millard S, Bray DF, Rood SB (2006) Stomatal characteristics of riparian poplar species in a semi-arid environment. Tree Physiol 26:211–218
  • Pérez Harguindeguy N, Díaz S, Garnier E, Lavorel S, Poorter H, Jaureguiberry P, Bret-Harte SM, Cornwell WK, Craine JM, Gurvich DE et al (2013) New handbook for standardised measurement of plant functional traits worldwide. Aust J Bot 61:167–234
  • Pérez-López U, Mena-Petite A, Muñoz Rueda A (2012) Interaction between salinity and elevated CO2: a physiological approach. Prog Bot 73:97–126
  • Petruzzellis F, Nardini A, Savi T, Tonet V, Castello M, Bacaro G (2018) Less safety for more efficiency: water relations and hydraulics of the invasive tree Ailanthus altissima (Mill.) Swingle compared with native Fraxinus ornus L., Tree Physiol. https://doi.org/10.1093/treephys/tpy076
  • Poorter H, Niinemets Ü, Poorter L, Wright IJ, Villar R (2009) Causes and consequences of variation in leaf mass per area (LMA): a meta-analysis. New Phytol 182:565–588
  • Rachmilevitch S, Da Costa M, Huang B (2006) Physiological and biochemical indicators for stress tolerance. In: Huang B (ed) Plant–environment interactions, 3rd edn. CRC Press, Boca Raton, FL, pp 321–356
  • Raimondo FM, Geraci A (2003) A new taxonomic arrangement in Sicilia Brassica sect. Brassica (Cruciferae). Fl Medit 12:439–441
  • Raimondo FM, Mazzola P (1997) A new taxonomic arrangement of the Sicilian members of Brassica sect Brassica. Lagascalia 19:831–838
  • Raimondo FM, Mazzola P, Ottonello D (1991) On the taxonomy and distribution of Brassica sect. Brassica (Cruciferae) in Sicily. Fl Medit 1:63–86
  • Sack L, Cowan PD, Jaikumar N, Holbrook NM (2003) The ‘hydrology’ of leaves: co-ordination of structure and function in temperate woody species. Plant Cell Environ 26:1343–1356
  • Sack L, Tyree MT, Holbrook NM (2005) Leaf hydraulic architecture correlates with regeneration irradiance in tropical rainforest trees. New Phytol 167:403–413
  • Sage RF, Sharkey TD, Seemann JR (1989) Acclimation of photosynthesis to elevated CO₂ in five C₃ species. Plant Physiol 89:590–596
  • Savi T, Love VL, Dal Borgo A, Martellos S, Nardini A (2017) Morpho-anatomical and physiological traits in saplings of drought-tolerant Mediterranean woody species. Trees 31:1137–1148
  • Schulze ED, Robichaux RH, Grace J, Rundel PW, Ehleringer JR (1987) Plant water balance. Bioscience 37:30–37
  • Scoppola A, Spampinato G (2005) Stato delle conoscenze sulla flora vascolare d’Italia—Atlante delle specie a rischio di estinzione. Versione 1.0. In: Scoppola A, Blasi C (eds) Stato delle conoscenze sulla flora vascolare d’Italia. Palombi Editori, Roma.
  • Sellin A (1999) Does pre-dawn water potential reflect conditions of equilibrium in plant and soil water status? Acta Oecol 20:51–59
  • Shengxin C, Chunxia L, Xuyang Y, Song C, Xuelei J, Xiaoying L, Zhigang X, Rongzhan G (2016) Morphological, photosynthetic, and physiological responses of rapeseed leaf to different combinations of red and blue lights at the rosette stage. Front Plant Sci 7:1144. https://doi.org/10.3389/fpls.2016.01144
  • Siddiqui ZS, Khan MA, Gi Kim B, Huang JS, Kwon TR (2008) Physiological responses of Brassica napus genotypes to combined drought and salt stress. Plant Stress 2:78–83
  • Singh DP, Singh P, Kumar A, Sharma HC (1985) Transpirational cooling as a screening technique for drought tolerance in oil seed Brassicas. Ann Bot 56:815–820
  • Slatyer RO (1962) Internal water relations of higher plants. Annu Rev Plant Physiol 13(1):351–378
  • Snogerup S, Gustaffson M, Bothmer RV (1990) Brassica sect. Brassica (Brassicaceae) I. Taxonomy and variation. Willdenowia 19:271–365
  • Tanentzap FM, Stempel A, Ryser P (2015) Reliability of leaf relative water content (RWC) measurements after storage: consequences for in situ measurements. Botany 93:535–541
  • Trifilò P, Gascó A, Raimondo F, Nardini A, Salleo S (2003) Kinetics of recovery of leaf hydraulic conductance and vein functionality from cavitation-induced embolism in sunflower. J Exp Bot 54:2323–2330
  • Tyree MT, Hammel HT (1972) The measurement of the turgor pressure and the water relations of plants by the pressure-bomb technique. J Exp Bot 23:267–282
  • Valladares F, Sanchez-Gomez D, Zavala MA (2006) Quantitative estimation of phenotypic plasticity: bridging the gap between the evolutionary concept and its ecological applications. J Ecol 94:1103–1116
  • von Bothmer R, Gustafsson M, Snogerup S (1995) Brassica sect. Brassica (Brassicaceae) II. Inter- and intraspecific crosses with cultivars of B. oleracea. Genet Resour Crop Ev 42:165–178
  • Wood JG (1934) The physiology of xerophytism in Australian plants: the stomatal frequencies, transpiration and osmotic pressures of sclerophyll and tomentose-succulent leaved plants. J Ecol 22:69–87
  • Yamori W, Hikosaka K, Way DA (2014) Temperature response of photosynthesis in C3, C4, and CAM plants: temperature acclimation and temperature adaptation. Photosynth Res 119:101–117
  • Zaghdoud C, Mota-Cadenas C, Carvajal M, Muries B, Ferchichi A, Martínez-Ballesta M (2013) Elevated CO₂ alleviates negative effects of salinity on broccoli (Brassica oleracea L. var. italica) plants by modulating water balance through aquaporins abundance. Environ Exp Bot 95:15–24
  • Zhang X, Lu G, Long W, Zou X, Li F, Nishio T (2014) Recent progress in drought and salt tolerance studies in Brassica crops. Breeding Sci 64:60–73
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