The impact of winter flooding with saline water on foliar carbon uptake and the volatile fraction of leaves and fruits of lemon (Citrus × limon) trees
Violeta Velikova A B , Tommaso La Mantia C , Marco Lauteri A , Marco Michelozzi D , Isabel Nogues A and Francesco Loreto E FA Consiglio Nazionale delle Ricerche – Istituto di Biologia Agroambientale e Forestale, Porano, Terni 05010, Italy.
B Bulgarian Academy of Sciences – Institute of Plant Physiology and Genetics, 1113 Sofia, Bulgaria.
C Universita’ di Palermo – Dipartimento di Colture Arboree, Facoltà di Agraria, Palermo 90128, Italy.
D Consiglio Nazionale delle Ricerche – Istituto di Genetica Vegetale, Sesto Fiorentino, Firenze 50019, Italy.
E Consiglio Nazionale delle Ricerche – Istituto per la Protezione delle Piante, Sesto Fiorentino, Firenze 50019, Italy.
F Corresponding author. Email: francesco.loreto@ipp.cnr.it
Functional Plant Biology 39(3) 199-213 https://doi.org/10.1071/FP11231
Submitted: 13 October 2011 Accepted: 30 December 2011 Published: 14 March 2012
Abstract
We investigated the consequences of recurrent winter flooding with saline water on a lemon (Citrus × limon (L.) Burm.f.) orchard, focussing on photosynthesis limitations and emission of secondary metabolites (isoprenoids) from leaves and fruits. Measurements were carried out immediately after flooding (December), at the end of winter (April) and after a dry summer in which plants were irrigated with optimal quality water (September). Photosynthesis was negatively affected by flooding. The effect was still visible at the end of winter, whereas the photosynthetic rate was fully recovered after summer, indicating an unexpected resilience capacity of flooded plants. Photosynthesis inhibition by flooding was not due to diffusive limitations to CO2 entry into the leaf, as indicated by measurements of stomatal conductance and intercellular CO2 concentration. Biochemical and photochemical limitations seemed to play a more important role in limiting the photosynthesis of flooded plants. In young leaves, characterised by high rates of mitochondrial respiration, respiratory rates were enhanced by flooding. Flooding transiently caused large and rapid emission of several volatile isoprenoids. Emission of limonene, the most abundant compound, was stimulated in the leaves, and in young and mature fruits. Flooding changed the blend of emitted isoprenoids, but only few changes were observed in the stored isoprenoids pool.
Additional keywords: Citrus, isoprenoids, photosynthesis.
References
Allahverdiev AI, Irandoust S, Andersson M (1999) Chromatographic separation of α-pinene isomerization products. Journal of Chromatography. A 848, 297–303.| Chromatographic separation of α-pinene isomerization products.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXltVykurw%3D&md5=3dd20507e97af9ccafc387495d2ebf0eCAS |
Arbona V, Hossain Z, López-Climent MF, Pérez-Clemente RM, Gómez-Cadenas A (2008) Antioxidant enzymatic activity is linked to waterlogging stress tolerance in citrus. Physiologia Plantarum 132, 452–466.
| Antioxidant enzymatic activity is linked to waterlogging stress tolerance in citrus.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXksFWktb8%3D&md5=3297fd7c3fdb6ed63c089acca01bf66aCAS |
Arbona V, López-Climent MF, Pérez-Clemente RM, Gómez-Cadenas A (2009) Maintenance of a high photosynthetic performance is linked to flooding tolerance in citrus. Environmental and Experimental Botany 66, 135–142.
| Maintenance of a high photosynthetic performance is linked to flooding tolerance in citrus.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXivVWksLc%3D&md5=0a38f3a7c31750595f4aa439c73d214aCAS |
Baker NR, Harbinson J, Kramer DM (2007) Determining the limitations and regulation of photosynthetic energy transduction in leaves. Plant, Cell & Environment 30, 1107–1125.
| Determining the limitations and regulation of photosynthetic energy transduction in leaves.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtVeiurrI&md5=e1f14e1297ba0efc99651b5e1da69e6eCAS |
Bilger W, Björkman O (1991) Temperature dependence of violaxanthin deepoxidation and non-photochemical fluorescence quenching in intact leaves of Gossypium hirsutum L. and Malva parviflora L. Planta 184, 226–234.
| Temperature dependence of violaxanthin deepoxidation and non-photochemical fluorescence quenching in intact leaves of Gossypium hirsutum L. and Malva parviflora L.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXkt1KitbY%3D&md5=f9119387a5fbf94c3c35dab3daca8186CAS |
Calvert DV (1982) Effect of ground water quality on crops in Florida. In ‘Proceedings of the Specialty Conference on Environmentally Sound Water and Soil Management. American Society of Chemical Engineering, Orlando, FL, 20–23 July 1982 ’. pp. 440–444. (American Society of Civil Engineers (ASCE): New York)
Centritto M, Loreto F, Chartzoulakis K (2003) The use of low [CO2] to estimate diffusional and non-diffusional limitations of photosynthetic capacity of salt-stressed olive saplings. Plant, Cell & Environment 26, 585–594.
| The use of low [CO2] to estimate diffusional and non-diffusional limitations of photosynthetic capacity of salt-stressed olive saplings.Crossref | GoogleScholarGoogle Scholar |
Choi WI, Lee SG, Park HM, Ahn YJ (2004) Toxicity of plant essential oils to Tetranychus urticae (Acari: Tetranychidae) and Phytoseiulus persimilis (Acari: Phytoseiidae). Journal of Economic Entomology 97, 553–558.
| Toxicity of plant essential oils to Tetranychus urticae (Acari: Tetranychidae) and Phytoseiulus persimilis (Acari: Phytoseiidae).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXktFOgt7Y%3D&md5=9d3c0d93af60e1e2a89baa255f6af0f2CAS |
Cojocariu C, Esher P, Heinz-Haberle K, Matyssek R, Rennemberg H, Kreuzwieser J (2005) The effect of ozone on the emission of carbonyls from leaves of adult Fagus sylvatica. Plant, Cell & Environment 28, 603–611.
| The effect of ozone on the emission of carbonyls from leaves of adult Fagus sylvatica.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXkslKlu7s%3D&md5=8b2a0bc02c34a62eed791d06e24136e9CAS |
de Gouw JA, Howard CJ, Custer TG, Fall R (1999) Emissions of volatile organic compounds from cut grass and clover are enhanced during the drying process. Geophysical Research Letters 26, 811–814.
| Emissions of volatile organic compounds from cut grass and clover are enhanced during the drying process.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXivFWns7c%3D&md5=4314980409ec6ef4e6e4627ae95702f0CAS |
Di Vaio C, Graziani G, Gaspari A, Scaglione G, Nocerino S, Ritieni A (2010) Essential oils content and antioxidant properties of peel ethanol extract in 18 lemon cultivars. Scientia Horticulturae 126, 50–55.
| Essential oils content and antioxidant properties of peel ethanol extract in 18 lemon cultivars.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXps1WksbY%3D&md5=6f097b3be9a3af047f08be94d9a582d7CAS |
Dicke M, Baldwin IT (2010) The evolutionary context for herbivore-induced plant volatiles: beyond the “cry for help”. Trends in Plant Science 15, 167–175.
| The evolutionary context for herbivore-induced plant volatiles: beyond the “cry for help”.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXivFGnsrs%3D&md5=f371f0cb406d31d870ba0bef32b60fd0CAS |
Fares S, Mereu S, Scarascia Mugnozza G, Vitale M, Manes F, Frattoni M, Ciccioli P, Gerosa G, Loreto F (2009) The ACCENT-VOCBAS field campaign on biosphere–atmosphere interactions in a Mediterranean ecosystem of Castelporziano (Rome): site characteristics, climatic and meteorological conditions, and eco-physiology of vegetation. Biogeosciences 6, 1043–1058.
| The ACCENT-VOCBAS field campaign on biosphere–atmosphere interactions in a Mediterranean ecosystem of Castelporziano (Rome): site characteristics, climatic and meteorological conditions, and eco-physiology of vegetation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhtFWjtLrL&md5=c176c7b2f055f32f59f21e8a974d2e2dCAS |
Fares S, Gentner DR, Park J-H, Ormeno E, Karlik J, Goldstein AH (2011) Biogenic emission from Citrus species in California. Atmospheric Environment 45, 4557–4568.
| Biogenic emission from Citrus species in California.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXpt1ahtr4%3D&md5=f36c3059781d5886ba9fba1279e5b7fbCAS |
Farquhar GD, Sharkey TD (1982) Stomatal conductance and photosynthesis. Annual Review of Plant Physiology 33, 317–345.
| Stomatal conductance and photosynthesis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL38XktlKjs7o%3D&md5=da22d203cd0fb9354b13d7e4b0c02786CAS |
Farquhar GD, von Caemmerer S, Berry JA (1980) A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta 149, 78–90.
| A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3cXksVWrt7w%3D&md5=86fa277ef7ab49db199f09e329e2f6beCAS |
Fisher K, Phillips CA (2008) The use of essential oils as anti-microbials: is citrus the answer? Trends in Food Science & Technology 19, 156–164.
| The use of essential oils as anti-microbials: is citrus the answer?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXitVGntb4%3D&md5=80330a4d972a2ad9211292315c49b041CAS |
García-Sánchez F, Syvertsen JP, Gimeno V, Botía P, Pérez-Pérez JG (2007) Responses to flooding and drought stress by two citrus rootstock seedlings with different water-use efficiency. Physiologia Plantarum 130, 532–542.
| Responses to flooding and drought stress by two citrus rootstock seedlings with different water-use efficiency.Crossref | GoogleScholarGoogle Scholar |
Genty B, Briantains JM, Baker NR (1989) The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochimica et Biophysica Acta 990, 87–92.
| The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1MXhsFWntL4%3D&md5=b1e6f4f065fb1987a8ebc6ee811cafe8CAS |
Gershenzon J, Dudareva N (2007) The function of terpene natural products in the natural world. Nature Chemical Biology 3, 408–414.
| The function of terpene natural products in the natural world.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXms1SrsLc%3D&md5=1e5a4d8fb8458adafb84e99b985ca77dCAS |
Harborne JB (2001) Secondary metabolites: attracting pollinators. In ‘Encyclopedia of life science’. (John Wiley & Sons Ltd: Chichester)
Hatier J-H, Gould KS (2009) Anthocyanin functions in vegetative organs. In ‘Anthocyanins. Biosynthesis, functions, and aApplications’. (Eds KS Gould, KM Davies, C Winefield) pp. 1–20. (Springer Science+ Business Media: New York)
Hodges DM, Nozzolillo C (1996) Anthocyanin and anthocyanoplast content of cruciferous seedlings subjected to mineral nutrient deficiencies. Journal of Plant Physiology 147, 749–754.
| Anthocyanin and anthocyanoplast content of cruciferous seedlings subjected to mineral nutrient deficiencies.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28Xis1Gks7k%3D&md5=ad00d7b5edfb3e29281fb09f1f9df32aCAS |
Hossain Z, López-Climent MF, Arbona V, Pérez-Clemente RM, Gómez-Cadenas A (2009) Modulation of the antioxidant system in citrus under waterlogging and subsequent drainage. Journal of Plant Physiology 166, 1391–1404.
| Modulation of the antioxidant system in citrus under waterlogging and subsequent drainage.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhtVGhsL7M&md5=a589968d9a69e35032018c99df7c73c6CAS |
Hughes NM, Smith WK (2007) Seasonal photosynthesis and anthocyanin production in ten broadleaf evergreen species. Functional Plant Biology 34, 1072–1079.
| Seasonal photosynthesis and anthocyanin production in ten broadleaf evergreen species.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtlGrtLvE&md5=1b065e9292a048d569d92433eb868df0CAS |
Ientile R, La Mantia T, Massa B, Ruhl J (2011) I cambiamenti nell’ecosistema della Riserva Naturale di Vendicari e gli effetti sull’avifauna. (Ed Danaus)
Kennedy RA, Rumpho ME, Fox TC (1992) Anaerobic metabolism in plants. Plant Physiology 100, 1–6.
| Anaerobic metabolism in plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK38XmtlSjtbs%3D&md5=28c1943469da55adf0b480c0fde9b980CAS |
Kozlowski TT (1997) ‘Responses of woody plants to flooding and salinity.’ Tree Physiology Monograph No. 1 (Heron Publishing: Victoria, Canada)
Lambers H (2003) Dryland salinity: a key environmental issue in southern Australia. Plant and Soil 257, v–vii.
| Dryland salinity: a key environmental issue in southern Australia.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXpvVCqtLw%3D&md5=91b3f7b989fd8ffe164281e8f6d6bce7CAS |
Langenheim JH (1994) Higher plant terpenoids: a phytocentric overview of their ecological roles. Journal of Chemical Ecology 20, 1223–1280.
| Higher plant terpenoids: a phytocentric overview of their ecological roles.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2cXksFert7s%3D&md5=5f6f1bbd94cf9962eb3c5f572036483dCAS |
Levy Y, Syvertsen JP (2004) Irrigation water quality and salinity effects in citrus trees. Horticultural Reviews 30, 37–82.
Li H, Syvertsen JP, Mccoy CW, Stuart RJ, Schumann AW (2006) Water stress and root injury from simulated flooding and Diaprepes abbreviatus root weevil larval feeding in citrus. Soil Science 171, 138–151.
| Water stress and root injury from simulated flooding and Diaprepes abbreviatus root weevil larval feeding in citrus.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XitF2itLw%3D&md5=bf3a1557304fb26f3a3a304bd82d0a52CAS |
Lichtenthaler HK, Wellburn AR (1983) Determinations of total carotenoids and chlorophylls a and b of leaf extracts in different solvents. Biochemical Society Transactions 11, 591–592.
Loreti E, Poggi A, Novi G, Alpi A, Perata P (2005) A genome-wide analysis of the effects of sucrose on gene expression in Arabidopsis seedlings under anoxia. Plant Physiology 137, 1130–1138.
| A genome-wide analysis of the effects of sucrose on gene expression in Arabidopsis seedlings under anoxia.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXislOqs7g%3D&md5=ef471e40a08a1b3312be31dded144b6aCAS |
Loreto F, Schnitzler J-P (2010) Abiotic stresses and induced BVOCs. Trends in Plant Science 15, 154–166.
| Abiotic stresses and induced BVOCs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXivFGnsro%3D&md5=5779aa6abe17f0ccadbdddb3e953664cCAS |
Lota M-L, de Rocca Serra D, Tomi F, Jacquemond C, Casanova J (2002) Volatile components of peel and leaf oils of lemon and lime species. Journal of Agricultural and Food Chemistry 50, 796–805.
| Volatile components of peel and leaf oils of lemon and lime species.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xjt1Shtw%3D%3D&md5=1f8643f1f1c73a18099a5cc72348630aCAS |
Maas EV (1993) Salinity and citriculture. Tree Physiology 12, 195–216.
Maxwell K, Johnson GN (2000) Chlorophyll fluorescence – a practical guide. Journal of Experimental Botany 51, 659–668.
| Chlorophyll fluorescence – a practical guide.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXjtF2js74%3D&md5=1d462336648d2570f11ecf0f6e979e31CAS |
Moufida S, Marzouk B (2003) Biochemical characterization of blood orange, sweet orange, lemon, bergamot and bitter orange. Phytochemistry 62, 1283–1289.
| Biochemical characterization of blood orange, sweet orange, lemon, bergamot and bitter orange.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXitFait7k%3D&md5=b4dcedac5e2f9839fbac40c5b354b940CAS |
Müller P, Li X-P, Niyogi KK (2001) Non-photochemical quenching. A response to excess light energy. Plant Physiology 125, 1558–1566.
| Non-photochemical quenching. A response to excess light energy.Crossref | GoogleScholarGoogle Scholar |
Munns R (2002) Comparative physiology of salt and water stress. Plant, Cell & Environment 25, 239–250.
| Comparative physiology of salt and water stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xhslakurw%3D&md5=8558cb25c538a179db778e53069617f0CAS |
Nieves M, Martinez V, Cerdá A, Guillen MG (1990) Yield and mineral composition of “Verna” lemon trees as affected by salinity and rootstock combination. Journal of Horticultural Science 65, 359–366.
Nieves M, Ruiz D, Cerdá A (1992) Influence of rootstock-scion combination in lemon trees salt tolerance. In ‘Proceedings of the International Society Citriculture Acireale, Italy’. pp. 387–390.
Paranychianakis NV, Chartzoulakis KS (2005) Irrigation of Mediterranean crops with saline water: from physiology to management practices. Agriculture Ecosystems & Environment 106, 171–187.
| Irrigation of Mediterranean crops with saline water: from physiology to management practices.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhslehtL4%3D&md5=4e7f07d7f957aeb1ec8b227b47946a6bCAS |
Pirrotta C, Barbano MS (2011) Analysis of deformation structures in Pliocene and Quaternary deposits of the Hyblean Plateaux (south-eastern Sicily). Tectonophysics 499, 41–53.
| Analysis of deformation structures in Pliocene and Quaternary deposits of the Hyblean Plateaux (south-eastern Sicily).Crossref | GoogleScholarGoogle Scholar |
Pitman MG, Lauchli A (2002) Global impact of salinity and agricultural ecosystems. In ‘Salinity: environment – plants – molecules’. (Eds A Läuchli, U Lüttge). pp. 3–20. (Kluwer Academic Publishers: Dordrecht)
Prior LD, Grieve AM, Bevington KB, Slavich PG (2007) Long-term effects of saline irrigation water on “Valencia” orange trees: relationship between growth and yield, and salt levels in soil and leaves. Australian Journal of Agricultural Research 58, 349–358.
| Long-term effects of saline irrigation water on “Valencia” orange trees: relationship between growth and yield, and salt levels in soil and leaves.Crossref | GoogleScholarGoogle Scholar |
Ramsar (1971) In ‘Convention on Wetlands of International Importance Especially as Waterfowl Habitat, Ramsar (Iran), 2 February 1971’. UN Treaty Series No. 14583.
Reighard GL, Parker ML, Krewer GW, Beckman TG, Wood BW, Smith JE, Whiddon J (2001) Impact of hurricanes on peach and pecan orchards in the southeastern United States. HortScience 36, 250–252.
Salvatore A, Borkosky S, Willink E, Bardo’ N (2004) Toxic effects of lemon peel constituents on Ceratitis capitata. Journal of Chemical Ecology 30, 323–333.
| Toxic effects of lemon peel constituents on Ceratitis capitata.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXhs12rsLo%3D&md5=22dc4ab62eb8a2a5978b875169d982b9CAS |
Schaffer B, Andersen PC, Ploetz RC (1992) Responses of fruit trees to flooding. Horticultural Reviews 13, 257–313.
Serra S (2011) Opportunities for biocatalysis in the flavor, fragrance, and cosmetic industry. In ‘Biocatalysis for green chemistry and chemical process development’. (Eds J Tao, R Kazlauskas). pp. 221–254. (John Wiley & Sons: Hoboken, NJ)
Sharkey TD (1996) Emission of low molecular mass hydrocarbons. Trends in Plant Science 1, 78–82.
| Emission of low molecular mass hydrocarbons.Crossref | GoogleScholarGoogle Scholar |
Sharkey TD, Bernacchi CJ, Farquhar GD, Singsaas EL (2007) Fitting photosynthetic carbon dioxide response curves for C3 leaves. Plant, Cell & Environment 30, 1035–1040.
| Fitting photosynthetic carbon dioxide response curves for C3 leaves.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtVeiur3F&md5=7bda4421067b44395a56f22306beb5b7CAS |
Storey R, Walker RR (1999) Citrus and salinity. Scientia Horticulturae 78, 39–81.
| Citrus and salinity.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXnsFaisLY%3D&md5=194b2e76db4ec380cb0c06c1331b4850CAS |
Syversten JP, Yelenosky G (1988) Salinity can enhance freeze tolerance of citrus rootstock seedlings by modifying growth, water relations, and mineral nutrition. Journal of the American Society for Horticultural Science 113, 889–893.
Syvertsen JP, Lloyd J, Kriedemann PE (1988) Salinity and drought stress effects on foliar ion concentration, water relations, and photosynthetic characteristics of orchard citrus. Australian Journal of Agricultural Research 39, 619–627.
| Salinity and drought stress effects on foliar ion concentration, water relations, and photosynthetic characteristics of orchard citrus.Crossref | GoogleScholarGoogle Scholar |
Vartapetian BB (1991) Flood-sensitive plants under primary and secondary anoxia: ultrastructural metabolic responses. In ‘Plant life under oxygen deprivation’. (Eds MB Jackson, DD Davies, H Lambers). pp. 201–216. (SPB Academic Publishing: The Hague)
Wohlfahrt G, Bahn M, Haubner E, Horak I, Michaeler W, Rottmar K, Tappeiner U, Cernusca A (1999) Inter-specific variation of the biochemical limitation to photosynthesis and related leaf traits of 30 species from mountain grassland ecosystems under different land use. Plant, Cell & Environment 22, 1281–1296.
| Inter-specific variation of the biochemical limitation to photosynthesis and related leaf traits of 30 species from mountain grassland ecosystems under different land use.Crossref | GoogleScholarGoogle Scholar |
Wullschleger SD (1993) Biochemical limitations to carbon assimilation in C3 plants – a retrospective analysis of the A/Ci curves from 109 species. Journal of Experimental Botany 44, 907–920.
| Biochemical limitations to carbon assimilation in C3 plants – a retrospective analysis of the A/Ci curves from 109 species.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3sXkvFWnurk%3D&md5=171eb987fe1c1406d6409c7702e9c219CAS |
Yamasaki Y, Kunoh H, Yamamoto H, Akimitsu K (2007) Biological roles of monoterpene volatiles derived from rough lemon (Citrus jambhiri Lush) in citrus defense. Journal of General Plant Pathology 73, 168–179.
| Biological roles of monoterpene volatiles derived from rough lemon (Citrus jambhiri Lush) in citrus defense.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtVeqsbbI&md5=6c302a82ea1ac638d6fb1402f75dccfdCAS |