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Li Xin, Li Shan, Deng Liping, Li Ren, Yin Yafang, Zheng Jingming. Axial variation of characteristics of water conducting tissue in xylem of Catalpa bungei[J]. Journal of Beijing Forestry University, 2020, 42(1): 27-34. DOI: 10.12171/j.1000-1522.20190238
Citation: Li Xin, Li Shan, Deng Liping, Li Ren, Yin Yafang, Zheng Jingming. Axial variation of characteristics of water conducting tissue in xylem of Catalpa bungei[J]. Journal of Beijing Forestry University, 2020, 42(1): 27-34. DOI: 10.12171/j.1000-1522.20190238

Axial variation of characteristics of water conducting tissue in xylem of Catalpa bungei

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  • Received Date: May 28, 2019
  • Revised Date: September 01, 2019
  • Available Online: December 29, 2019
  • Published Date: January 13, 2020
  • ObjectiveThis paper intends to explore the axial variation of the anatomical structure of wood sapwood of Catalpa bungei, in order to deepen our understanding of the water conduction mechanism in broadleaved tree species, as well as to provide theoretical basis for the cultivation of C. bungei plantation, the protection of this precious tree species and the utilization of its wood.
    MethodThree trees of C. bungei were selected, sapwood samples were collected from tree height at 0, 1.3, 3.8, 6.3, 8.8 and 11.3 m, respectively. Meanwhile, sapwood area was measured, transverse and longitudinal sections of wood blocks were prepared. The anatomical traits of xylem such as vessel lumen diameter, vessel frequency were observed with light microscopy. Relationships among wood anatomical traits were tested by correlation analysis and analysis of variance, and axial changes of wood anatomical traits were analyzed by linear regression.
    Result(1) Earlywood vessel lumen diameter and vessel density do not change significantly with tree height, however, earlywood vessel lumen diameter decreased with height while vessel density had an opposite trend. Maximum vessel lumen diameter of early- and latewood, latewood vessel lumen diameter and pit membrane diameter varied significantly with tree height, which decreased with tree height. (2) Both sapwood area and hydraulic vessel diameter decreased significantly with tree height. (3) Both sapwood area and pit membrane diameter were significantly positively correlated with the hydraulic vessel diameter.
    ConclusionAxial variance of hydraulic structure of C. bungei is manifested in three aspects: sapwood area, vessel related traits and pit membrane properties. Growth ring of C. bungei was obvious, and the early and late vessel lumen diameter wood differed greatly with bigger variation of early wood than that of late wood. Axial variation of the maximum vessel lumen diameter, sapwood area and pit membrane diameter are significant for this tree species whereas axial variation of the vessel density is not significant. Taken together, wood at the base of C. bungei owned relatively large and sparse vessels and higher proportion of sapwood area compared to many small vessels and lower proportion of sapwood area in wood at the upper stem, and this architecture is an optimized structural design for the long-distance water transport function during xylem evolution, leading to reduction of embolization risk and improvement of efficiency and safety of water transport.
  • [1]
    张红霞, 袁凤辉, 关德新, 等. 维管植物木质部水分传输过程的影响因素及研究进展[J]. 生态学杂志, 2017, 36(11):289−296.

    Zhang H X, Yuan F H, Guan D X, et al. A review on water transport in xylem of vascular plants and its affecting factors[J]. Journal of Ecology, 2017, 36(11): 289−296.
    [2]
    Li S, Lens F, Espino S, et al. Intervessel pit membrane thickness as a key determinant of embolism resistance in angiosperm xylem[J]. IAWA Journal, 2016, 37(2): 152−171. doi: 10.1163/22941932-20160128
    [3]
    Ryan M G, Yoder B J. Hydraulic limits to tree height and tree growth[J]. Bioscience, 1997, 47(4): 235−242. doi: 10.2307/1313077
    [4]
    West G B, Brown J H, Enquist B J. A general model for the structure and allometry of plant vascular systems[J]. Nature, 1999, 400: 664−667.
    [5]
    Schuldt B, Leuschner C, Brock N, et al. Changes in wood density, wood anatomy and hydraulic properties of the xylem along the root-to-shoot flow path in tropical rainforest trees[J]. Tree Physiology, 2013, 33(2): 161−174. doi: 10.1093/treephys/tps122
    [6]
    Tommaso A, Vinicio C, Marco C, et al. Convergent tapering of xylem conduits in different woody species[J]. New Phytologist, 2006, 169(2): 279−290. doi: 10.1111/j.1469-8137.2005.01587.x
    [7]
    Anfodillo T, Petit G, Crivellaro A. Axial conduit widening in woody species: a still neglected anatomical pattern[J]. IAWA Journal, 2013, 34(4): 352−364. doi: 10.1163/22941932-00000030
    [8]
    Pfautsch S, Aspinwall M J, Drake J E, et al. Traits and trade-offs in whole-tree hydraulic architecture along the vertical axis of Eucalyptus grandis[J]. Annals of Botany, 2018, 121(1): 129−141. doi: 10.1093/aob/mcx137
    [9]
    Lechthaler S, Turnbull T L, Gelmini Y, et al. A standardization method to disentangle environmental information from axial trends of xylem anatomical traits[J]. Tree Physiology, 2019, 39(3): 495−502. doi: 10.1093/treephys/tpy110
    [10]
    Becker P, Gribben R J, Schulte P J. Incorporation of transfer resistance between tracheary elements into hydraulic resistance models for tapered conduits[J]. Tree Physiology, 2003, 23(15): 1009−1019. doi: 10.1093/treephys/23.15.1009
    [11]
    Petit G, Pfautsch S, Anfodillo T, et al. The challenge of tree height in Eucalyptus regnans: when xylem tapering overcomes hydraulic resistance[J]. New Phytologist, 2010, 187(4): 1146−1153. doi: 10.1111/j.1469-8137.2010.03304.x
    [12]
    Tyree M T, Zimmermann M H. Xylem structure and the ascent of sap[M]. Berlin: Springer, 2002: 45−56.
    [13]
    李荣, 姜在民, 张硕新, 等. 木本植物木质部栓塞脆弱性研究新进展[J]. 植物生态学报, 2015, 39(8):838−848. doi: 10.17521/cjpe.2015.0080

    Li R, Jiang Z M, Zhang S X, et al. A review of new research progress on the vulnerability of xylem embolism of woody plants[J]. Journal of Plant Ecology, 2015, 39(8): 838−848. doi: 10.17521/cjpe.2015.0080
    [14]
    Corothie H. Multilingual glossary of terms used in wood anatomy[M]. Amsterdam: IAWA, 1964: 43.
    [15]
    England J R, Attiwill P M. Changes in sapwood permeability and anatomy with tree age and height in the broad-leaved evergreen species Eucalyptus regnans[J]. Tree Physiology, 2007, 27(8): 1113−1124. doi: 10.1093/treephys/27.8.1113
    [16]
    Gerrish G. An explanation of natural forest dieback based on the “pipe model” analogy[J]. GeoJournal, 1988, 17(2): 295−299. doi: 10.1007/BF02432939
    [17]
    Pothier D, Margolis H A, Waring R H. Patterns of change of saturated sapwood permeability and sapwood conductance with stand development[J]. Canadian Journal of Forest Research, 1989, 19(4): 432−439. doi: 10.1139/x89-068
    [18]
    Coyea M R, Margolis H A. Factors affecting the relationship between sapwood area and leaf area of balsam fir[J]. Canadian Journal of Forest Research, 1992, 22: 1684−1693.
    [19]
    Fan Z, Cao K, Becker P. Axial and radial variations in xylem anatomy of angiosperm and conifer trees in Yunnan, China[J]. IAWA Journal, 2009, 30(1): 1−13. doi: 10.1163/22941932-90000198
    [20]
    范泽鑫, 曹坤芳, 邹寿青. 云南哀牢山6种常绿阔叶树木质部解剖特征的轴向和径向变化[J]. 植物生态学报, 2005, 29(6):968−975. doi: 10.3321/j.issn:1005-264X.2005.06.013

    Fan Z X, Cao K F, Zou S Q. Axial and radial changes in xylem anatomical characteristics in six evergreen broadleaved tree species in Ailao Mountain, Yunnan[J]. Chinese Journal of Plant Ecology, 2005, 29(6): 968−975. doi: 10.3321/j.issn:1005-264X.2005.06.013
    [21]
    Scholz A, Klepsch M, Karimi Z, et al. How to quantify conduits in wood?[J]. Frontiers in Plant Science, 2013, 4: 1−11.
    [22]
    Sperry J S, Nichols K L, Sullivan J E M, et al. Xylem embolism in ring-porous, diffuse-porous, and coniferous trees of northern Utah and interior Alaska[J]. Ecology, 1994, 75: 1736−1752. doi: 10.2307/1939633
    [23]
    Petit G, Anfodillo T, Mencuccini M. Tapering of xylem conduits and hydraulic limitations in sycamore (Acer pseudoplatanus) trees[J]. New Phytologist, 2008, 177(3): 653−664. doi: 10.1111/j.1469-8137.2007.02291.x
    [24]
    Petit G, Anfodillo T, Carraro V, et al. Hydraulic constraints limit height growth in trees at high altitude[J]. New Phytologist, 2011, 189(1): 241−252. doi: 10.1111/j.1469-8137.2010.03455.x
    [25]
    Petit G, Declerck F A J, Carrer M, et al. Axial vessel widening in arborescent monocots[J]. Tree Physiology, 2014, 34(2): 137−145. doi: 10.1093/treephys/tpt118
    [26]
    Petit G, Anfodillo T. Plant physiology in theory and practice: an analysis of the WBE model for vascular plants[J]. Journal of Theoretical Biology, 2009, 259(1): 1−4. doi: 10.1016/j.jtbi.2009.03.007
    [27]
    Lintunen A, Kalliokoski T. The effect of tree architecture on conduit diameter and frequency from small distal roots to branch tips in Betula pendula, Picea abies and Pinus sylvestris[J]. Tree Physiology, 2010, 30(11): 1433−1447. doi: 10.1093/treephys/tpq085
    [28]
    Bettiati D, Petit G, Anfodillo T. Testing the equi-resistance principle of the xylem transport system in a small ash tree: empirical support from anatomical analyses[J]. Tree Physiology, 2012, 32(2): 171−177. doi: 10.1093/treephys/tpr137
    [29]
    Olson M E, Soriano D, Rosell J A, et al. Plant height and hydraulic vulnerability to drought and cold[J]. Proceedings of the National Academy of Sciences, 2018, 115(29): 7551−7556. doi: 10.1073/pnas.1721728115
    [30]
    Cardoso S, Sousa V B, Quilhó T, et al. Anatomical variation of teakwood from unmanaged mature plantations in East Timor[J]. Journal of Wood Science, 2015, 61(3): 326−333. doi: 10.1007/s10086-015-1474-y
    [31]
    龚容, 徐霞江, 红蕾, 等. 干旱半干旱区几种典型灌木半灌木茎叶水分传导系统的结构特征[J]. 北京师范大学学报(自然科学版), 2018, 54(4):104−112.

    Gong R, Xu X J, Hong L, et al. Architectural traits of stem-leaf hydraulic system in typical shrubs in arid and semi-arid regions[J]. Journal of Beijing Normal University (Natural Science), 2018, 54(4): 104−112.
    [32]
    Zanne A E, Westoby M, Falster D S, et al. Angiosperm wood structure: global patterns in vessel anatomy and their relation to wood density and potential conductivity[J]. American Journal of Botany, 2010, 97(2): 207−215. doi: 10.3732/ajb.0900178
    [33]
    Fan D Y, Xie Z Q. Several controversial viewpoints in studying the cavitation of xylem vessels[J]. Acta Phytoecologica Sinica, 2004, 28(1): 126−132.
    [34]
    Schulte P J, Gibson A C. Hydraulic conductance and tracheid anatomy in six species of extant seed plants[J]. Canadian Journal of Botany, 1988, 66(6): 1073−1079. doi: 10.1139/b88-153
    [35]
    Aparecido L M T, Santos J D, Higuchi N, et al. Relevance of wood anatomy and size of Amazonian trees in the determination and allometry of sapwood area[J]. Acta Amazonica, 2019, 49(1): 1−10. doi: 10.1590/1809-4392201800961
    [36]
    Köstner B, Falge E, Tenhunen J D. Age-related effects on leaf area/sapwood area relationships, canopy transpiration and carbon gain of Norway spruce stands (Picea abies) in the Fichtelgebirge, Germany[J]. Tree Physiology, 2002, 22(8): 567−574. doi: 10.1093/treephys/22.8.567
    [37]
    Gebauer T, Horna V, Leuschner C. Variability in radial sap flux density patterns and sapwood area among seven co-occurring temperate broad-leaved tree species[J]. Tree Physiology, 2008, 28(12): 1821−1830. doi: 10.1093/treephys/28.12.1821
    [38]
    Meinzer F C, Bond B J, Warren J M, et al. Does water transport scale universally with tree size?[J]. Functional Ecology, 2005, 19(4): 558−565. doi: 10.1111/j.1365-2435.2005.01017.x
    [39]
    Bass P, Ewers F W, Davis S D, et al. Evolution of xylem physiology[M]// Hemsle A R, Poole I. The evolution of plant physiology. New York: Academic Press, 2004.
    [40]
    Jean-Christophe D, Barbara L, Meinzer F C. Bordered pit structure and function determine spatial patterns of air-seeding thresholds in xylem of Douglas-fir (Pseudotsuga menziesii, Pinaceae) trees[J]. American Journal of Botany, 2006, 93(11): 1588−1600. doi: 10.3732/ajb.93.11.1588
    [41]
    Cochard H, Holtta T, Herbette S, et al. New insights into the mechanisms of water-stress-induced cavitation in conifers[J]. Plant Physiology, 2009, 151(2): 949−954. doi: 10.1104/pp.109.138305
    [42]
    Delzon S, Douthe C, Sala A, et al. Mechanism of water-stress induced cavitation in conifers: bordered pit structure and function support the hypothesis of seal capillary-seeding[J]. Plant, Cell & Environment, 2010, 33(12): 2101−2111.
    [43]
    木巴热克·阿尤普, 荆卫民, 伊丽米努尔, 等. 柽柳属6种植物侧枝木质部导水率与纹孔数量特征关系[J]. 西北林学院学报, 2017, 32(2):106−111. doi: 10.3969/j.issn.1001-7461.2017.02.18

    Mubarek A, Jing W M, Yiliminuer, et al. Relations between xylem hydraulic efficiency and inter-vessel pit features of six Tamarix L. species[J]. Journal of Northwest Forestry University, 2017, 32(2): 106−111. doi: 10.3969/j.issn.1001-7461.2017.02.18
    [44]
    Wheeler J K, Sperry J S, Hacke U G, et al. Inter-vessel pitting and cavitation in woody Rosaceae and other vesselled plants: a basis for a safety versus efficiency trade-off in xylem transport[J]. Plant, Cell & Environment, 2005, 28(6): 800−812.
    [45]
    Christman M A, Sperry J S, Adler F R. Testing the ‘rare pit’ hypothesis for xylem cavitation resistance in three species of Acer[J]. New Phytologist, 2009, 182(3): 664−674. doi: 10.1111/j.1469-8137.2009.02776.x
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