Skip to main content
Log in

Physiological performance and biomass production of two ornamental shrub species under deficit irrigation

  • Original Paper
  • Published:
Trees Aims and scope Submit manuscript

Abstract

Key message

This study shows that deficit irrigation can be encouraged in productive activities like plant nursing, especially with the most resistant species.

Abstract

Drought acclimation is attained by avoidance mechanisms in the short term and by adaptation changes in the long term. In this study, we applied deficit irrigation at nursery stage to elicit species-specific physiological responses and biomass production in two ornamental shrub species, comparing two settings: open air (OA) and greenhouse (GH). Viburnum opulus L. and Photinia x fraseri ‘Red robin’ were compared under three irrigation levels: severe water deficit (SWD), moderate water deficit (MWD) and control (C). In both experiments, SWD induced lower values of water potentials in both species whereas MWD had similar effects to C. In OA, SWD reduced earlier stomatal conductance in V. opulus and photosynthesis rate in P. x fraseri and in GH V. opulus showed a reduction of gas exchange even in MWD. P. x fraseri showed greater stomatal control capacity. In contrast, treatments did not affect PSII efficiency even if P. x fraseri proved a greater capacity to differentiate the I–P phase of the fluorescence transient in SWD conditions. In both experiments, SWD and MWD affected leaf area by lowering the number of leaves in P. x fraseri and reducing leaf surface in V. opulus. Moreover, V. opulus showed early leaf senescence and premature fall. Deficit irrigation had effects also on leaf characteristics: smaller leaf area unit in V. opulus, reduced biomass and leaf mass per area and succulence in both species, increase of spongy tissue thickness. Eventually, we can state that P. x fraseri can withstand 30 % evapotranspiration, while maintaining functionality.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

Similar content being viewed by others

References

  • Anyia AO, Herzog H (2004) Water-use efficiency, leaf area and leaf gas exchange of cowpeas under mid-season drought. Eur J Agron 20:327–339

    Article  Google Scholar 

  • Brunetti M, Buffoni L, Mangianti F, Maugeri M, Nanni T (2004) Temperature, precipitation and extreme events during the last century in Italy. Glob Planet Change 40:141–149

    Article  Google Scholar 

  • Bruschi P, Vendramin G, Bussotti F, Grossoni P (2000) Morphological and Molecular Differentiation between Quercus petraea (Matt.) Liebl. And Quercus pubescens Willd. (Fagaceae) in Northern and Central Italy. Ann Bot Lond 85:325–333

    Article  Google Scholar 

  • Bussotti F (2008) Functional leaf traits, plant communities and acclimation processes in relation to oxidative stress in trees: a critical overview. Glob Change Biol 14:2727–2739

    Google Scholar 

  • Bussotti F, Gravano E, Grossoni P, Tani C (1998) Occurrence of tannins in leaves of beech trees (Fagus sylvatica) along an ecological gradient, detected by histochemical and ultrastructural analyses. New Phytol 138:469–479

    Article  CAS  Google Scholar 

  • Bussotti F, Pancrazi M, Matteucci G, Gerosa G (2005) Leaf morphology and chemistry in Fagus sylvatica (beech) trees as affected by site factors and ozone: results from CONECOFOR permanent monitoring plots in Italy. Tree Physiol 25:211–219

    Article  CAS  PubMed  Google Scholar 

  • Centritto M, Tognetti R, Leitgeb E, Střelcová K, Cohen S (2011) Above ground processes: anticipating climate change influences. In: Bredemeier M, Cohen S, Godbold DL, Lode E, Pilcher V, Schleppi P (eds) Forest Management and the water cycle: an ecosystem-based approach Ecological Studies 212. Springer, Berlin, pp 31–64

    Google Scholar 

  • Ceulemans R, van Praet L, Jiang XN (1995) Effects of CO2 enrichment leaf position and clone on stomatal index and epidermal cell density in poplar (Populus). New Phytol 131:99–107

    Article  Google Scholar 

  • Chaves MM, Pereira JS, Maroco J, Rodrigues ML, Ricardo CPP, Osorio ML, Carvalho I, Faria T, Pinheiro C (2002) How plants cope with water stress in the field. Photosynthesis and growth. Ann Bot Lond 89:907–916

    Article  CAS  Google Scholar 

  • Cornic C, Fresnau C (2002) Photosynthetic carbon reduction and carbon oxidation cycles are the main electron sinks for Photosystem II activity during a mild drought. Ann Bot Lond 89:887–894

    Article  CAS  Google Scholar 

  • Davies ZG, Edmondson JL, Heinemeyer A, Leake JR, Gaston KJ (2011) Mapping an urban ecosystem service:quantifying above-ground carbon storage at a city-wide scale. J Appl Ecol 48:1125–1134

    Article  CAS  Google Scholar 

  • Desotgiu R, Cascio C, Pollastrini M, Gerosa G, Marzuoli R, Bussotti F (2012) Chlorophyll a fluorescence analysis along a vertical gradient of the crown in a poplar (Oxford clone) subjected to ozone and water stress. Tree Physiol 32:976–986

    Article  CAS  PubMed  Google Scholar 

  • Desotgiu R, Cascio C, Pollastrini M, Gerosa G, Marzuoli R, Bussotti F (2013) Responses to ozone on Populus Oxford clone in an open top chamber experiment assessed before sunrise and in full sunlight. Photosynthetica 51:267–280

    Article  CAS  Google Scholar 

  • Edwards DR, Dixon MA (1995) Mechanisms of drought response in Thuja occidentalis L. I. Water stress conditioning and osmotic adjustment. Tree Physiol 15:121–127

    Article  PubMed  Google Scholar 

  • Fan S, Blake TJ, Blumwald E (1994) The relative contribution of elastic and osmotic adjustments to turgor maintenance of woody species. Physiol Plantarum 90:408–413

    Article  Google Scholar 

  • Flexas J, Medrano H (2002) Drought-inhibition of photosynthesis in C3 plants: stomatal and non-stomatal limitations revisited. Ann Bot Lond 89:183–189

    Article  CAS  Google Scholar 

  • Fraser LH, Greenall A, Carlyle C, Turkington R, Ross Friedman C (2009) Adaptive phenotypic plasticity of Pseudoroegneria spicata: response of stomatal density, leaf area and biomass to changes in water supply and increased temperature. Ann Bot Lond 103:769–775

    Article  Google Scholar 

  • Galmés J, Flexas J, Savé R, Medrano H (2007) Water relations and stomatal characteristics of Mediterranean plants with different growth forms and leaf habits: responses to water stress and recovery. Plant Soil 290:139–155

    Article  Google Scholar 

  • Garnier E, Shipley B, Roumet C, Laurent G (2001) A standardized protocol for the determination of specific leaf area and leaf dry matter content. Funct Ecol 15:688–695

    Article  Google Scholar 

  • Gebre GM, Kuhns MR, Brandle JR (1994) Organic solute accumulation and dehydration tolerance in three water-stressed Populus deltoides clones. Tree Physiol 14:575–587

    Article  CAS  PubMed  Google Scholar 

  • Giorgi F, Lionello P (2008) Climate change projections for the Mediterranean region. Glob Planet Change 63:90–104

    Article  Google Scholar 

  • Giorio P, Sorrentino G, d’Andria R (1999) Stomatal behaviour, leaf water status and photosynthetic response in field-grown olive trees under water deficit. Environ Exp Bot 42:95–104

    Article  Google Scholar 

  • Jo HK (2002) Impacts of urban greenspace on offsetting carbon emissions for middle Korea. J Environ Manage 64:115–126

    Article  PubMed  Google Scholar 

  • Kozlowski TT, Pallardy SG (2002) Acclimation and adaptive responses of woody plants to environmental stresses. Bot Rev 68:270–334

    Article  Google Scholar 

  • Lawlor DW, Cornic G (2002) Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant Cell Environ 25:275–294

    Article  CAS  PubMed  Google Scholar 

  • Lionello P, Planton S, Rodo X (2008) Trends and climate change in the Mediterranean region. Glob Planet Change 63:87–89

    Article  Google Scholar 

  • Maherali H, Pockman WT, Jackson RB (2004) Adaptive variation in the vulnerability of woody plants to xylem cavitation. Ecology 85:2184–2199

    Article  Google Scholar 

  • Martínez-Vilalta J, Prat E, Oliveras I, Pinol J (2002) Xylem hydraulic properties of roots and stems of nine Mediterranean woody species. Oecologia 133:19–29

    Article  PubMed  Google Scholar 

  • Mediavilla S, Escudero A (2003) Stomatal response to drought at a Mediterranean site: a comparative study of co-occurring woody species differing in leaf longevity. Tree Physiol 23:987–996

    Article  PubMed  Google Scholar 

  • Mediavilla S, Escudero A, Heilmeier H (2001) Internal leaf anatomy and photosynthetic resource-use efficiency: interspecific and intraspecific comparisons. Tree Physiol 21:251–259

    Article  CAS  PubMed  Google Scholar 

  • Medrano H, Escalona M, Bota J, Gulías J, Flexas J (2002) Regulation of photosynthesis of C3 plants in response to progressive drought: stomatal conductance as a reference parameter. Ann Bot Lond 89:895–905

    Article  CAS  Google Scholar 

  • Medrano H, Flexas J, Galmés J (2009) Variability in water use efficiency at the leaf level among Mediterranean plants with different growth forms. Plant Soil 317:17–29

    Article  CAS  Google Scholar 

  • Morgan JM (1984) Osmoregulation and water stress in higher plants. Annu Rev Plant Physiol 35:299–319

    Article  Google Scholar 

  • Nanni T, Brunetti M, Maugeri M (2007) Variazioni nella frequenza e nell’intensità delle precipitazioni giornaliere in Italia negli ultimi 120 anni. In: Carli B, Cavarretta G, Colacino M, Fuzzi S (eds.) Clima e cambiamenti climatici: le attività di ricerca del CNR. Consiglio Nazionale delle Ricerche, Roma. ISBN 9788880800750

  • Nowak DJ, Crane DE (2002) Carbon storage and sequestration by urban trees in the USA. Environ Pollut 116:381–389

    Article  CAS  PubMed  Google Scholar 

  • Oukarroum A, Schansker G, Strasser RJ (2009) Drought stress effects on photosystem I content and photosystem II thermotolerance analyzed using Chl a fluorescence kinetics in barley varieties differing in their drought tolerance. Physiol Plantarum 137:188–199

    Article  CAS  Google Scholar 

  • Pallardy SG (2008) Physiology of Woody Plants. Academic Press, San Diego, p 454

    Google Scholar 

  • Pollastrini M, Desotgiu R, Camin F, Ziller L, Marzuoli R, Gerosa G, Bussotti F (2013) Intra-annual pattern of photosynthesis, growth and stable isotope partitioning in a poplar clone subjected to ozone and water stress. Water Air Soil Poll 224:1761–1772

    Article  Google Scholar 

  • Pollastrini M, Desotgiu R, Camin F, Ziller L, Gerosa G, Marzuoli R, Bussotti F (2014) Severe drought events increase the sensitivity to ozone on poplar clones. Environ Exp Bot 100:94–104

    Article  CAS  Google Scholar 

  • Rubio G, Vilagrosa A, Cortina J, Bellot J (2001) Modificaciones morfofisiológica en plantones de Pistacia lentiscus y Quercus rotundifolia como consecuencia del endurecimiento hídrico en vivero. Efectos sobre supervivencia y crecimiento en campo. Granada. Actas del III Congreso Forestal Español 3:527–532

    Google Scholar 

  • Savé R, Castell C, Terradas J (1999) Gas exchange and water relations. In: Roda F, Retana J, Gracia CA, Bellot J (eds) Ecology of mediterranean evergreen oak forests. Springer, Berlin, pp 135–147

    Chapter  Google Scholar 

  • Schansker G, Srivastava A, Strasser RJ (2003) Characterization of the 820-nm transmission signal paralleling the chlorophyll a fluorescence rise (OJIP) in pea leaves. Funct Plant Biol 30:785–796

    Article  CAS  Google Scholar 

  • Shashua-Bar L, Pearlmutter Erell E (2011) The influence of trees and grass on outdoor thermal comfort in a hot-arid environment. Int J Climatol 31:1498–1506

    Article  Google Scholar 

  • Shashua-Bar L, Pearlmutter D, Erell E (2009) The cooling efficiency of urban landscape strategies in a hot dry climate. Landscape Urban Plan 92:179–186

    Article  Google Scholar 

  • Socìas FX, Correìa MJ, Medrano H (1997) The role of abscissic acid and water relations in drought responses of subterranean clover. J Exp Bot 48:1281–1288

    Article  Google Scholar 

  • Strasser RJ, Srivastava A, Tsimilli-Michael M (2000) The fluorescence transient as a tool to characterize and screen photosynthetic samples. In: Yunus M, Pathre U, Mohanty P (eds) Probing photosynthesis: mechanism, regulation and adaptation, Chapter 25. Taylor and Francis, London, pp 443–480

    Google Scholar 

  • Strasser RJ, Tsimilli-Michael M, Srivastava A (2004) Analysis of the chlorophyll fluorescence transient. In: Papageorgiou GC (ed) Chlorophyll a fluorescence: a signature of photosynthesis. Springer, Dordrecht, pp 321–362

    Chapter  Google Scholar 

  • Strasser RJ, Tsimilli-Michael M, Qiang S, Goltsev V (2010) Simultaneous in vivo recording of prompt and delayed fluorescence and 820-nm reflection changes during drying and after rehydration of the resurrection plant Haberlea rhodopensis. Biochim Biophys Acta 1797:1313–1326

    Article  CAS  PubMed  Google Scholar 

  • Struve DK, Ferrini F, Fini A, Pennati L (2009) Relative growth and water use of seedlings from three Italian Quercus species. Arboric Urban For 35:113–121

    Google Scholar 

  • Susca T, Gaffin SR, Dell’Osso GR (2011) Positive effects of vegetation: urban heat island and green roofs. Environ Pollut 159:2119–2126

    Article  CAS  PubMed  Google Scholar 

  • Tejero IG, Zuazo Durán VH, Bocanegra Jiménez JA, Fernández Muriel JL (2011) Improved water-use efficiency by deficit-irrigation programmes: implications for saving water in citrus orchards. Sci Hortic-Amsterdam 128:274–282

    Article  Google Scholar 

  • Tezara W, Marín O, Rengifo E, Martínez D, Herrera A (2005) Photosynthesis and photoinhibition in two xerophytic shrubs during drought. Photosynthetica 43:37–45

    Article  CAS  Google Scholar 

  • Tognetti R, d’Andria R, Sacchi R, Lavini A, Morelli G, Alvino A (2007) Deficit irrigation affects seasonal changes in leaf physiology and oil quality of Olea europaea (cultivars Frantoio and Leccino). Ann Appl Biol 150:169–189

    Article  Google Scholar 

  • Tognetti R, Giovannelli A, Lavini A, Morelli G, Fragnito F, d’Andria R (2009) Assessing environmental controls over conductances through the soil–plant-atmosphere continuum in an experimental olive tree plantation of southern Italy. Agr Forest Meteorol 149:1229–1243

    Article  Google Scholar 

  • Ugolini F, Tognetti R, Bussotti F, Raschi A, Ennos AR (2014a) Wood hydraulic and mechanical properties induced by low water availability on two ornamental species Photinia x fraseri var. Red Robin and Viburnum opulus L. Urban For Urban Green 13:158–165

    Article  Google Scholar 

  • Ugolini F, Massetti L, Pedrazzoli F, Tognetti R, Vecchione A, Zulini L, Maresi G (2014b) Ecophysiological responses and vulnerability to other pathologies in European chestnut coppices, heavily infested by the Asian chestnut gall wasp. Forest Ecol Manag 314:38–49

    Article  Google Scholar 

  • UNESCO (2014) World Water Development Programme, water and energy, vol 1. UNESCO, Paris, p 230

    Google Scholar 

  • Vilagrosa A, Villar-Salvador P, Puértolas J (2006) El endurecimiento en vivero de especies forestales mediterráneas. In: Cortina J (ed) Calidad de planta forestal para la restauración en ambientes mediterráneos. Estado actual de conocimiento. Ministerio de Medio Ambiente. Serie forestal, Madrid, pp 119–140

    Google Scholar 

  • Villar-Salvador P, Ocaña L, Peñuelas J, Carrasco I (1999) Effect of water stress conditioning on the water relations, root growth capacity, and the nitrogen and non-structural carbohydrate concentration of Pinus halepensis Mill. (Aleppo pine) seedlings. Ann For Sci 56:459–465

    Article  Google Scholar 

  • Villar-Salvador P, Planelles R, Oliet J, Peñuelas-Rubira JL, Jacobs DF, González M (2004) Drought tolerance and transplanting performance of holm oak (Quercus ilex) seedlings after drought hardening in the nursery. Tree Physiol 24:1147–1155

    Article  PubMed  Google Scholar 

Download references

Author contribution statement

Francesca Ugolini planned the experiments, carried out the field measurements and data analysis and is the first author of the manuscript. Filippo Bussotti and Antonio Raschi were supervisors of the whole project. Anthony Roland Ennos and Roberto Tognetti allowed the performance of some analysis performed during the study (e.g., hydraulic conductivity) and made a cross-revision of the manuscript.

Acknowledgments

We thank Giorgio Maresi, from Fondazione Edmund Mach, Mario Lanini, from the Institute of Biometeorology, Nicola and Paolo Marzialetti from the Centre for Experimental Nursing, for their support and knowledge transfer in the sector of plant nursing.

Conflict of interest

Authors declare that they have no conflict of interest and no funding has been received to perform this study.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Francesca Ugolini.

Additional information

Communicated by K. Masaka.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ugolini, F., Bussotti, F., Raschi, A. et al. Physiological performance and biomass production of two ornamental shrub species under deficit irrigation. Trees 29, 407–422 (2015). https://doi.org/10.1007/s00468-014-1120-0

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00468-014-1120-0

Keywords

Navigation