Skip to main content
Log in

Water transport distance’s effect on tylose development and sap flow in Meili grapevine

  • Original Article
  • Published:
Brazilian Journal of Botany Aims and scope Submit manuscript

Abstract

Grape pruning may lead not only to some physical damages to the xylem vessels but also to the tylose blockage in these vessels. However, there is little information on vessel lumens blockage by tylose decreasing the original capability of sap flow transportation. In present studies, to elucidate the effect of tyloses on both water transport during xylem development and variations in hydraulic conductance with increasing distance of water transport, shoots of three different-shaped vines were evaluated in this study, based on observation of tylose developments and sap flow measurements. The study showed that, for different-shaped vines, sap flow transport distance was significantly associated with quantity of tyloses. Vessels of cordon training (CT) vines had the largest percentage of partly and completely blocked vessels among three different-shaped vines, up to 65.4% and 33.2%, respectively. For renewal crawled cordon training (rCCT) and perennial crawled cordon training (pCCT) vines, shoots of perennial branches (pCCT) had a larger percentage of partly and completely blocked vessels (39.7% and 16.7%, respectively) than shoot of current-year shoots (rCCT vines, 35.6% and 9.3%, respectively). Sap flow rates and sap flow transport distances had a negative correlation for sap flow rates of same-shaped vines. In addition, sap flow rates and sap flow transport distances (namely, number of nodes) and/or quantity of tyloses varied during different-shaped vines. Overall, vessels with few tyloses showed significantly higher values of hydraulic conductance than vessels were completely or partially occluded by more tyloses.

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

Similar content being viewed by others

References

  • Beckman C (1987) The nature of wilt diseases of plants. APS Press, St Paul

    Google Scholar 

  • Beckman CH, Talboys PW (1981) Anatomy of resistance. In: Mace ME, Bell AA, Beckman CH (eds) Fungal wilt diseases of plants. Academic Press, New York, pp 487–521

    Chapter  Google Scholar 

  • Bonsen KJM, Kucera LJ (1990) Vessel occlusion in plants: morphological functional and evolutionary aspects. IAWA 11:393–399

    Article  Google Scholar 

  • Brown GE, Kirkham T, Lancaster R (1995) The pruning of trees, shrubs and conifers. Timber, Portland

    Google Scholar 

  • Canny MJ (1997) Tyloses and the maintenance of transpiration. Ann Bot 80:565–570

    Article  Google Scholar 

  • Carlquist SJ (1975) Ecological strategies of xylem evolution. University of California Press, Oakland

    Google Scholar 

  • Cochard H, Coll L, Roux XL, Améglio T (2002) Unraveling the effects of plant hydraulics on stomatal closure during water stress in walnut. Plant Physiol 128:282–290

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Cohen S, Naor A (2002) The effect of three rootstocks on water use, canopy conductance and hydraulic parameters of apple trees and predicting canopy from hydraulic conductance. Plant Cell Environ 25:17–28

    Article  Google Scholar 

  • Collins BR, Parke JL, Lachenbruch B, Hansen EM (2009) The effects of Phytophthora ramorum infection on the hydraulic conductivity and tylosis formation in tanoak sapwood. Can J For Res 39:1766–1776

    Article  Google Scholar 

  • Delzon S, Loustau D (2005) Age-related decline in stand water use: sap flow and transpiration in a pine forest chronosequence. Agr For Meteorol 129:105–119

    Article  Google Scholar 

  • Ford CR, Mcguire MA, Mitchell RJ, Teskey RO (2004) Assessing variation in the radial profile of sap flux density in Pinus species and its effect on daily water use. Tree Physiol 24:241–249

    Article  PubMed  Google Scholar 

  • Green SR, Clothier BE, McLeod DJ (1997) The response of sap flow in apple roots to localised irrigation. Agric Water Manag 33:63–78

    Article  Google Scholar 

  • Greven M, Neal S, Green S, Dichio B, Clothier B (2009) The effects of drought on the water use, fruit development and oil yield from young olive trees. Agric Water Manag 96:1525–1531

    Article  Google Scholar 

  • Halis Y, Djehichi S, Senoussi MM (2012) Vessel development and the importance of lateral flow in water transport within developing bundles of current-year shoots of grapevine (Vitis vinifera L.). Trees 26:705–714

    Article  Google Scholar 

  • Jedrzejuk A, Zakrzewski J (2009) Xylem occlusions in the stems of common lilac during postharvest life. Acta Physiol Plant 31:1147–1153

    Article  Google Scholar 

  • Kang SZ, Hu XT, Du TS, Zhang JH, Jerie P (2003) Transpiration coefficient and ratio of transpiration to evapotranspiration of pear tree (Pyrus communis L.) under alternative partial root-zone drying conditions. Hydrol Process 17:1165–1176

    Article  Google Scholar 

  • Kitin PB, Fujii T, Abe H, Funada R (2004) Anatomy of the vessel network within and between tree rings of Fraxinus lanuginose (Oleaceae). Am J Bot 91:779–788

    Article  PubMed  Google Scholar 

  • Leuzinger ST, Krner C (2007) Water savings in mature deciduous forest trees under elevated CO2. Glob Change Biol 13:1–11

    Article  Google Scholar 

  • Liu XZ, Kang SZ, Li FS (2009) Simulation of artificial neural network model for trunk sap flow of Pyrus pyrifolia and its comparison with multiple-linear regression. Agric Water Manag 96:939–945

    Article  Google Scholar 

  • Lu P, Muller WJ, Chacko EK (2000) Spatial variations in xylem sap flux density in the trunk of orchard-grown, mature mango trees under changing soil water conditions. Tree Physiol 20:683–692

    Article  PubMed  Google Scholar 

  • McElrone AJ, Grant JA, Kluepfel DA (2010) The role of tyloses in crown hydraulic failure of mature walnut trees afflicted by apoplexy disorder. Tree Physiol 30:761–772

    Article  PubMed  Google Scholar 

  • Meuser J, Frensch J (1998) Hydraulic properties of living late metaxylem and interactions between transpiration and xylem pressure in maize. J Exp Bot 49:69–77

    Article  CAS  Google Scholar 

  • Mitchell PJ, Veneklaas E, Lambers H, Burgess SSO (2009) Partitioning of evapotranspiration in a semi-arid eucalypt woodland in south-western Australia. Agric For Meteorol 149:25–37

    Article  Google Scholar 

  • Moreno F, Fernandez JE, Clothier BE, Green SR (1996) Transpiration and root water uptake by olive trees. Plant Soil 184:85–96

    Article  CAS  Google Scholar 

  • Morton L (2000) Viticulture and grapevine declines: lessons of black goo. Phytopathol Mediterr 39:59–67

    Google Scholar 

  • Muhammad AF, Sattle R (1982) Vessel structure of Gnetum and the origin of angiosperms. Am J Bot 69:1004–1021

    Article  Google Scholar 

  • Mundy DC, Manning MA (2011) Physiological response of grapevines to vascular pathogens: a review. N Z Plant Prot 64:7–16

    Google Scholar 

  • Parameswaran N, Knigge H, Liese W (1985) Electron microscopic demonstration of a suberised layer in the tylosis wall of beech and oak. IAWA Bull 6:269–271

    Article  Google Scholar 

  • Parke JL, Oh E, Voelker S, Hansen EM, Buckles G, Lachenbruch B (2007) Phytophthora ramorum colonizes tanoak xylem and is associated with reduced stem water transport. Am Phytopathol Soc 97:1558–1567

    Article  CAS  Google Scholar 

  • Pataki DE, Oren R (2003) Species differences in stomatal control of water loss at the canopy scale in a mature bottomland deciduous forest. Adv Water Resour 26:1267–1278

    Article  Google Scholar 

  • Ranjani K, Krishnamurthy KV (1988) Tyloses of the root wood of Cassia fistula L. Feddes Repert 99:147–149

    Google Scholar 

  • Ruzin SE (1999) Plant microtechnique and microscopy. Oxford University, New York, p 322

    Google Scholar 

  • Saitoh TJ, Ohtani J, Fukazawa K (1993) The occurrence and morphology of tyloses and gums in the vessels of Japanese hardwoods. IAWA 14:359–371

    Article  Google Scholar 

  • Sakuratani T (1981) A heat balance method for measuring water flux in the stem of intact plants. J Agric Meteorol 37:9–17

    Article  Google Scholar 

  • Salleo S, Nardini A, Gullo MAL, Ghirarrdelli LA (2002) Changes in stem and leaf hydraulics preceding leaf shedding in Castanea sativa L. Biol Plantarum 45:227–234

    Article  Google Scholar 

  • Schepper VD, Steppe K, Labeke MCV, Lemeu R (2010) Detailed analysis of double girdling effects on stem diameter variations and sap flow in young oak trees. Environ Exp Bot 68:149–156

    Article  Google Scholar 

  • Schmitt U, Liese W (1993) Response of xylem parenchyma by suberization in some hardwoods after mechanical injury. Trees 8:23–30

    Article  Google Scholar 

  • Schulte PJ, Renée Brooks R (2003) Branch junctions and the flow of water through xylem in Douglas-fir and ponderosa pine stems. J Exp Bot 54:1597–1605

    Article  CAS  PubMed  Google Scholar 

  • Scott PC, Miller LW, Webster BD, Leopold AC (1967) Structural changes during bean leaf abscission. Am J Bot 54:730–734

    Article  Google Scholar 

  • Sellami MH, Sifaoui MS (2003) Estimating transpiration in an intercropping system: measuring sap flow inside the oasis. Agric Water Manag 59:191–204

    Article  Google Scholar 

  • Shang NK (2011) Negative pressure transport mechanism of long-distance water transport in trees. Shandong For Sci Technol 3:90–92

    Google Scholar 

  • Sun YL, Shen FY (2008) Study on dissection structure and contact angle of vessels between nodes and internodes in three kinds of trees. J Anhui Agric Sci 36:7131–7132

    Google Scholar 

  • Sun Q, Rost TL, Matthews MA (2006) Pruning-induced tylose development in stems of current-year shoots of Vitis vinifera (Vitaceae). Am J Bot 93:1567–1576

    Article  CAS  PubMed  Google Scholar 

  • Sun Q, Rost TR, Matthews MA (2008) Wound-induced vascular occlusions in Vitis vinifera (Vitaceae): tyloses in summer and gels in winter. Am J Bot 95:1498–1505

    Article  PubMed  Google Scholar 

  • Sun Q, Sun YL, Walker MA, Labavitch JM (2013) Vascular occlusions in grapevines with Pierce’s disease make disease symptom development worse. Plant Physiol 161:1529–1541

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Taneda H, Tateno M (2007) Effects of transverse movement of water in xylem on patterns of water transport within current-year shoots of kudzu vine, Pueraria lobata. Funct Ecol 21:226–234

    Article  Google Scholar 

  • Wang HT, Zhao WF, Ma LY (2006) Spatial variation of sap flow of Platycladus orientalis and it’s affecting factors. Sci Silv Sin 42:2127

    Google Scholar 

  • Webster BD (1973) Anatomical and histochemical changes in leaf abscission. In: Kozlowski TT (ed) Shedding of plant parts. Academic Press, New York, pp 45–83

    Chapter  Google Scholar 

  • Wilson KB, Hanson PJ, Mulholland PJ, Baldocchi DD, Wullschleger SD (2001) A comparison of methods for determining forest evapotranspiration and its components: sap-flow, soil water budget, eddy covariance and catchment water balance. Agric For Meteorol 106:153–168

    Article  Google Scholar 

  • Wu CN (1989) The discussion on the problem of water rise to the tops of the trees. Zhejiang For Sci Technol 9:63

    Google Scholar 

  • Wullschleger SD, King AW (2000) Radial variation in sap velocity as a function of stem diameter and sapwood thickness in a yellow-poplar tree. Tree Physiol 20:511–518

    Article  PubMed  Google Scholar 

  • Zhang DW, Shi FC (2004) Morphological anatomical studies on Betulaceae vessel element from Heilong Jiang Prov. China. Bull Bot Res 24(2):158–161

    Google Scholar 

Download references

Acknowledgements

This project was supported by Shandong Province Natural science Fund (ZR2015CL038) and Tai’an city’s Science and Technology Development Project (2017GX0058), and the authors also thank Technology extension service center of forest and fruit industries in Turpan for their kindly support.

Author information

Authors and Affiliations

Authors

Contributions

XHZ designed the study; XHZ, LYL and CXL conducted laboratory experiments; XHZ and CXL analyzed the data; XHZ and LYL wrote the manuscript; and LYL reviewed the manuscript. HL supervised the research project.

Corresponding author

Correspondence to Hua Li.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zhao, X., Liu, L., Li, C. et al. Water transport distance’s effect on tylose development and sap flow in Meili grapevine. Braz. J. Bot 42, 261–269 (2019). https://doi.org/10.1007/s40415-019-00523-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40415-019-00523-4

Keywords

Navigation