Skip to main content

Advertisement

Log in

Water relations of climbing ivy in a temperate forest

  • Original Article
  • Published:
Planta Aims and scope Submit manuscript

Abstract

Ivy (Hedera helix) is the most important liana in temperate European forests. We studied water relations of adult ivy in a natural, 35 m tall mixed deciduous forest in Switzerland using a construction crane to access the canopy. Predawn leaf water potential at the top of climbing ivy ranged from −0.4 to −0.6 MPa, daily minima ranged from −1.3 to −1.7 MPa. Leaf water potentials as well as relative sap flow were held surprisingly constant throughout different weather conditions, suggesting a tendency to isohydric behaviour. Maximum stomatal conductance was 200 mmol m−2 s−1. The use of a potometer experiment allowed us to measure absolute transpiration rates integrated over a whole plant of 0.23 mmol m−2 s−1. Nightly sap flow of ivy during warm, dry nights accounted for up to 20% of the seasonal maximum. Maximum sap flow rates were reached at ca. 0.5 kPa vpd. On the other hand, the host trees showed a less conservative stomatal regulation, maximum sap flow rates were reached at vpd values of ca. 1 kPa. Sap flow rates of ivy decreased by ca. 20% in spring after bud break of trees, suggesting that ivy profits strongly from warm sunny days in early spring before budbreak of the host trees and from mild winter days. This species may benefit from rising winter temperatures in Europe and thus become a stronger competitor against its host trees.

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

Similar content being viewed by others

Abbreviations

A:

Sap wood area

b:

Reference conductance at 1 kPa

g s :

Stomatal conductance

g c :

Canopy conductance

m:

Vpd sensitivity

PAR:

Photosynthetically active radiation

SF:

Sap flow

vpd:

Vapour pressure deficit

WSD:

Water saturation deficit

α:

Fitting parameters for the non-linear fit between SF and vpd

β:

Fitting parameters for the non-linear fit between SF and vpd

ψ:

Leaf water potential

References

  • Andergassen S, Bauer H (2002) Frost hardiness in the juvenile and adult life phase of ivy (Hedera helix L.). Plant Ecol 161:207–213

    Article  Google Scholar 

  • Asshoff R, Zotz G, Körner C (2006) Growth and phenology of mature temperate forest trees in elevated CO2. Glob Change Biol 12:848–861

    Article  Google Scholar 

  • Biggerstaff MS, Beck CW (2007) Effects of method of English ivy removal and seed addition on regeneration of vegetation in a southeastern piedmont forest. Am Midl Nat 158:206–220

    Article  Google Scholar 

  • Bush SE, Hultine KR, Sperry JS, Ehleringer JR (2010) Calibration of thermal dissipation sap flow probes for ring- and diffuse-porous trees. Tree Physiol 30:1545–1554

    Article  PubMed  Google Scholar 

  • Caird MA, Richards JH, Donovan LA (2007) Nighttime stomatal conductance and transpiration in C3 and C4 plants. Plant Physiol 143:4–10

    Article  PubMed  CAS  Google Scholar 

  • Carter GA, Teramura AH (1988) Vine photosynthesis and relationships to climbing mechanics in a forest understory. Am J Bot 75:1011–1018

    Article  Google Scholar 

  • Cech PG, Pepin S, Körner C (2003) Elevated CO2 reduces sap flux in mature deciduous forest trees. Oecologia 137:258–268

    Article  PubMed  Google Scholar 

  • Christman MA, Donovan LA, Richards JH (2009) Magnitude of nighttime transpiration does not affect plant growth or nutrition in well-watered Arabidopsis. Physiol Plant 135:264–273

    Article  Google Scholar 

  • Clark DB, Clark DA (1990) Distribution and effects on tree growth of lianas and woody hemiepiphytes in a Costa Rican tropical wet forest. J Trop Ecol 6:321–331

    Article  Google Scholar 

  • Cramer MD, Hawkins HJ, Verboom GA (2009) The importance of nutrient regulation of plant water flux. Oecologia 161:15–24

    Article  PubMed  Google Scholar 

  • Elias P (1979) Contribution to the eco physiological study of the water relations of forest shrubs. Preslia 51:77–90

    Google Scholar 

  • Ewers FW, Fisher JB, Fichtner K (1991) Water flux and xylem structure in vines. In: Putz FE, Mooney HA (eds) Biology of vines. Cambridge University Press, Cambridge, pp 127–160

    Google Scholar 

  • Fischer A, Feller U (1994) Seasonal changes in the pattern of assimilatory enzymes and the proteolytic activities in leaves of juvenile ivy. Ann Bot 74:389–396

    Article  CAS  Google Scholar 

  • Granados J, Körner C (2002) In deep shade, elevated CO2 increases the vigor of tropical climbing plants. Glob Change Biol 8:1109–1117

    Article  Google Scholar 

  • Granier A (1985) A new method of sap flow measurement in tree stems. Ann Sci For 42:193–200

    Article  Google Scholar 

  • Hättenschwiler S, Körner C (2000) Tree seedling responses to in situ CO2-enrichment differ among species and depend on understorey light availability. Glob Change Biol 6:213–226

    Article  Google Scholar 

  • Hättenschwiler S, Körner C (2003) Does elevated CO2 facilitate naturalization of the non-indigenous Prunus laurocerasus in Swiss temperate forests? Funct Ecol 17:778–785

    Article  Google Scholar 

  • Heuzé P, Dupouey J-L, Schnitzler A (2009) Radial growth response of Hedera helix to hydrological changes and climatic variability in the Rhine floodplain. River Res Appl 25:393–404

    Article  Google Scholar 

  • Iversen J (1944) Viscum, Hedera and Ilex as climate indicators. Eologiska Föreningens Förhandlingar 66:463–483

    Google Scholar 

  • Keel SG, Pepin S, Leuzinger S, Körner C (2007) Stomatal conductance in mature deciduous forest trees exposed to elevated CO2. Trees 21:151–159

    Article  Google Scholar 

  • Körner C (2004) Through enhanced tree dynamics carbon dioxide enrichment may cause tropical forests to lose carbon. Philos Trans Roy Soc B 359:493–498

    Article  Google Scholar 

  • Körner C, Bannister P (1985) Stomatal responses to humidity in Northofagus menziesii. N Z J Bot 23:425–429

    Google Scholar 

  • Körner C, Basler D (2010) Phenology under global warming. Science 327:1461–1462

    Article  PubMed  Google Scholar 

  • Körner C, Scheel A, Bauer H (1979) Maximum leaf diffusive conductance in vascular plants. Photosynthetica 13:45–82

    Google Scholar 

  • Leuzinger S, Körner C (2007) Water savings in mature deciduous forest trees under elevated CO2. Glob Change Biol 13:2498–2508

    Article  Google Scholar 

  • Leuzinger S, Zotz G, Asshoff R, Körner C (2005) Responses of deciduous forest trees to severe drought in Central Europe. Tree Physiol 25:641–650

    PubMed  Google Scholar 

  • Metcalfe DJ (2005) Hedera helix (L.), biology of the British Isles. J Ecol 93:632–648

    Article  Google Scholar 

  • Mitchell AF (1975) Three forest climbers. Forestry Commission Forest Record 102. Her Majesty’s Stationery Office, London

    Google Scholar 

  • Mohan JE, Ziska LH, Schlesinger WH, Thomas RB, Sicher RC, George K, Clark JS (2006) Biomass and toxicity responses of poison ivy (Toxicodendron radicans) to elevated atmospheric CO2. Proc Natl Acad Sci USA 103:9086–9089

    Article  PubMed  CAS  Google Scholar 

  • Monteith JL (1995) A reinterpretation of stomatal response to humidity. Plant Cell Environ 18:357–364

    Article  Google Scholar 

  • OcCC (2008) Das Klima ändert sich—was nun? Der neue UN-Klimabericht (IPCC 2007) und die wichtigsten Ergebnisse aus Sicht der Schweiz. OcCC —Organe consultatif sur les changements climatiques, Bern. ISBN 978-3-907630-33-4

  • Oren R, Sperry JS, Katul GG, Ewers BE, Pataki DE, Phillips N, Schäfer KVR (1999) Survey and synthesis of intra- and interspecific responses of canopy stomatal conductance to vapour pressure deficit. Plant Cell Environ 22:1515–1526

    Article  Google Scholar 

  • Parker J (1962) Relationships among cold hardiness, watersoluble protein, anthocyanins and free sugars in Hedera helix L. Plant Physiol 37:809–813

    Article  PubMed  CAS  Google Scholar 

  • Pataki DA, Oren R, Tissue DT (1998) Elevated carbon dioxide does not affect average canopy stomatal conductance of Pinus taeda L. Oecologia 117:47–52

    Article  Google Scholar 

  • Putz FE (1984) The natural history of lianas on Barro Colorado Island, Panama. Ecology 65:1713–1724

    Article  Google Scholar 

  • Putz FE, Holbrook M (1991) Biomechanical studies of vines. In: Putz FE, Mooney HA (eds) Biology of vines. Cambridge University Press, Cambridge, pp 73–98

    Google Scholar 

  • R Development Core Team (2009) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna

  • Ringold PL, Magee TK, Peck DV (2008) Twelve invasive plant taxa in US western riparian ecosystems. J N Am Benthol Soc 27:949–966

    Article  Google Scholar 

  • Schnitzer SA, Bongers F (2002) The ecology of lianas and their role in forests. Trends Ecol Evol 17:223–230

    Article  Google Scholar 

  • Schnitzler A, Heuzé P (2006) Ivy (Hedera helix L.) dynamics in riverine forests: effects of river regulation and forest disturbance. For Ecol Manag 236:12–17

    Article  Google Scholar 

  • Steppe K, De Pauw DJW, Doody TM, Teskey RO (2010) A comparison of sap flux density using thermal dissipation, heat pulse velocity and heat field deformation methods. Agric For Meteorol 150:1046–1056

    Article  Google Scholar 

  • Tank AMGK, Wijngaard JB, Konnen GP et al (2002) Daily dataset of 20th-century surface air temperature and precipitation series for the European Climate Assessment. Int J Climatol 22:1441–1453

    Article  Google Scholar 

  • Tanner W, Beevers H (2001) Transpiration, a prerequisite for long-distance transport of minerals in plants? Proc Natl Acad Sci USA 98:9443–9447

    Article  PubMed  CAS  Google Scholar 

  • Zhu SD, Cao KF (2010) Contrasting cost-benefit strategy between lianas and trees in a tropical seasonal rain forest in southwestern China. Oecologia 163:591–599

    Article  PubMed  Google Scholar 

  • Zotz G, Cueni N, Körner C (2006) In situ growth stimulation of a temperate zone liana (Hedera helix) in elevated CO2. Funct Ecol 20:763–769

    Article  Google Scholar 

Download references

Acknowledgments

We would like to thank E. Amstutz and O. Bignuccolo for crane operation and logistic help. Further, we thank S. Keel for providing us with stomatal conductance data of host trees. This work is part of a Master’s Thesis conducted by A. H. Funding came from the Swiss National Science Foundation projects 3100-059769.99 and 5005-65755 (NCCR Climate) granted to C. K. The Swiss Canopy Crane is funded by the Swiss Agency for the Environment, Forest and Landscape. Funding for S. L. partially came from the FP7 project ‘ACQWA’.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to S. Leuzinger.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Leuzinger, S., Hartmann, A. & Körner, C. Water relations of climbing ivy in a temperate forest. Planta 233, 1087–1096 (2011). https://doi.org/10.1007/s00425-011-1363-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00425-011-1363-6

Keywords

Navigation