|Table of Contents|

Relationship Between Leaf Area Index and Both Light Use Efficiency and Water Use Efficiency Across Individuals of Salix matsudana

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2020年01
Page:
62-68
Research Field:
Publishing date:

Info

Title:
Relationship Between Leaf Area Index and Both Light Use Efficiency and Water Use Efficiency Across Individuals of Salix matsudana
Author(s):
CHEN Jing1HU Guoxian1ZHOU Jiansong1ZHAO Chengzhang2
(1.College of Environment and Resources,Wenshan University,Wenshan,Yunnan 663099;2.College of Geography and Environmental Science,Northwest Normal University/Research Center of Wetland Resources Protection and Industrial Development Engineering of Gansu Province,Lanzhou,Gansu 730070)
Keywords:
leaf area indexlight use efficiencywater use efficiencysize calssesSalix matsudana
PACS:
-
DOI:
10.11937/bfyy.20191312
Abstract:
The study area was located in the floodplain wetlands of Zhangye city in the Heihe River basin in northwest China (100.40° E,38.98° N).According to d (the cube root of plant volume) at the Heihe flood plain of Zhangye city,Salix matsudana was divided into 3 size classes,small individuals (I,d250 cm),medium individuals (II,250 cm320 cm),and standardized major axis (SMA) tests were used to examine the relationship of single plant leaf area index (LAI) with light use efficiency (LUE) and water use efficiency (WUE) of Salix matsudana at 3 size classes.The results showed that with the size classes turned from I to III,LAI,gap fraction threshold,photosynthetic active radiation and air temperature increased,and air relative humidity decreased.The height,leaf area,leaf coverage,net photosynthetic rate,transpiration rate and WUE of Salix matsudana increase,while bifurcation angle,leaf thickness and LUE decreased gradually.Stomatal conductance displayed an ‘inverted U-shaped’ trend.LAI had a positive and negative correlation with LUE and WUE at I and III (P<0.05),respectively,while there were significant positive relationship between LAI and both LUE and WUE at II(P<0.05).Moderate LAI,LUE and WUE were used by medium-sized plant at II,and less or larger LAI and photosynthetic efficiency by which number holds sway above the flux were selected by small or large individual at I and III,which reflected the optimization allocation mode between spatial pattern of leaves and resource use efficiency of wetland plant in different size classes.

References:

[1]GANOPOLSKI A,KUBATZKI C,CLAUSSEN M,et al.The influence of vegetation-atmosphere-ocean interaction on climate during the mid-Holocene[J].Science,1998,280(5371):1916-1919.[2]ARORA V.Modeling vegetation as a dynamic component in soil-vegetation-atmosphere transfer schemes and hydrological models[J].Reviews of Geophysics,2002,40(2):1-26.[3]卫亚星,王莉雯.青海省植被光能利用率模拟研究[J].生态学报,2010,30(19):5209-5216.[4]WARING R H,RUNNING S W.Forest ecosystems analysis at multiple scales[M].New York:Academic Press,1998.[5]何春霞,李吉跃,孟平,等.4种高大树木的叶片性状及WUE随树高的变化[J].生态学报,2013,33(18):5644-5654.[6]GAO Y,ZHU X J,YU G R,et al.Water use efficiency threshold for terrestrial ecosystem carbon sequestration in China under afforestation[J].Agricultural and Forest Meteorology,2014,195-196(15):32-37.[7]PRICE C A,WEITZ J S.Allometric covariation:A hallmark behavior of plants and leaves[J].New Phytologist,2012,193(4):882-889.[8]BARTHLMY D,CARAGLIO Y.Plant architecture:A dynamic,multilevel and comprehensive approach to plant form,structure and ontogeny[J].Annuals of Botany,2007,99(3):375-407.[9]GALIA S N,ROELOFJ O,JORDIEJC N,et al.Biomass allocation and leaf life span in relation to light interception by tropical forest plants during the first years of secondary succession[J].Journal of Ecology,2010,96(6):1211-1221.[10]MASEYK K S,LIN T,ROTENBERG E,et al.Physiology-phenology interactions in a productive semi-arid pine forest[J].New Phytologist,2008,178(3):603-616.[11]王景旭,丁丽霞,程乾.湿地植被叶面积指数对光化学指数和光能利用率关系的影响:基于实测数据和PROSPECT-SAIL模型[J].自然资源学报,2016,31(3):514-525.[12]李辉东,关德新,袁凤辉,等.科尔沁草甸生态系统水分利用效率及影响因素[J].生态学报,2015,35(2):478-488.[13]陈静,赵成章,王继伟,等.不同密度旱柳的树冠构型与光截获[J].植物生态学报,2017,41(6):661-669.[14]夏江宝,张淑勇,赵自国,等.贝壳堤岛旱柳光合效率的土壤水分临界效应及其阈值分级[J].植物生态学报,2013,37(9):851-860.[15]SONG X X,FANG J,HAN X J,et al.Overexpression of quinone reductase from Salix matsudana Koidz enhances salt tolerance in transgenic Arabidopsis thaliana[J].Gene,2016,576(3):520-527.[16]杨晓东,阎恩荣,张志浩,等.浙江天童常绿阔叶林演替阶段共有种的树木构型[J].植物生态学报,2013,37(7):611-619.[17]WESTOBY M,REICH P B,WRIGHT I J.Understanding ecological variation across species:Area-based vs.mass-based expression of leaf traits[J].New Phytologist,2013,199(2):322-323.[18]隋雪梅,辛晓平,张宏斌,等.呼伦贝尔贝加尔针茅草甸草原光能利用率变化规律分析[J].中国农业资源与区划,2013,34(5):27-35.[19]KUMAR R,SAYAWGI A K,RAMOS C,et al.Partitioning of dry matter during drought stress in rainfed lowland rice[J].Field Crops Res,2006,96(2):455-465.[20]WEINER J.Allocation,plasticity and allometry in plants[J].Perspectives in Plant Ecology Evolution and Systematics,2004,6(4):207-215.[21]NIKLAS K J,ENQUIST B J.Canonical rules for plant organ biomass partitioning and annual allocation[J].American Journal of Botany,2002,89(5):812-819.[22]SHENG W P,REN S J,YU G R,et al.Patterns and driving factors of WUE and NUE in natural forest ecosystems along the northsouth transect of eastern China[J].J Geogr Sci,2011,21(4):651-665.[23]MURCHIE E H,NIYOGI K K.Manipulation of photoprotection to improve plant photosynthesis[J].Plant Physiology,2011,155:86-92.[24]MCCULLOH K A,SPERRY J S.Patterns in hydraulic architecture and their implications for transport efficiency[J].Tree Physiology,2005,25(3):257-267.[25]孙伟,王德利,王立,等.狗尾草蒸腾特性与水分利用效率对模拟光辐射增强和CO2浓度升高的响应[J].植物生态学报,2003,27(4):448-453.[26]DAZ S,HODGSON J G,Thompson K.The plant traits that drive ecosystems:Evidence from three continents[J].Journal of Vegetation Science,2004,15:295-304..

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Last Update: 2020-01-14