Sex-Related Differences of Ginkgo biloba in Growth Traits and Wood Properties

Ginkgo biloba is one of the most widely cultivated dioecious timber trees in China. Understanding sex-related differences and how they affect growth traits and wood properties is crucial for informed management and optimal utilization of ginkgoes. In the present study, we collected 42 ginkgo samples and conducted DNA molecular identification to determine their sex. The result was a 1:1 ratio of male to female specimens. In addition, we measured 16 growth-trait and wood-property indices for these samples using advanced equipment, such as X-ray diffraction (XRD) and the Hitman ST300 standing tree tool. For growth traits, significant differences were observed between male and female ginkgoes in terms of the diameter at breast height (DBH), clear bole height (CBH), height, and volume. Significant differences were identified in wood properties between male and female ginkgoes in terms of the degree of cellulose crystallinity (DCC), cell length, cell wall thickness, and wall-to-lumen ratio. Tracheids from female trees were found to be wider, with thicker cell walls, than those from male trees. Principal component analysis (PCA) showed that there was a slight separation between the sexes in terms of all growth traits, whereas there was no separation in wood properties. The membership function value (MFV) also showed that male ginkgo exhibited a more robust phenotype than female ginkgo. The selection of male ginkgo for breeding and utilization offers distinct advantages for practical production.

[1]  Changjun Ding,et al.  Xylem anatomical and hydraulic traits vary within crown but not respond to water and nitrogen addition in Populus tomentosa , 2023, Agricultural Water Management.

[2]  Yanjun Li,et al.  Change in Micro-Morphology and Micro-Mechanical Properties of Thermally Modified Moso Bamboo , 2022, Polymers.

[3]  Junhui Wang,et al.  Genetic Evaluation and Combined Selection for the Simultaneous Improvement of Growth and Wood Properties in Catalpa bungei Clones , 2021, Forests.

[4]  Joshua E. Elias,et al.  Precise regulation of the relative rates of surface area and volume synthesis in bacterial cells growing in dynamic environments , 2021, Nature Communications.

[5]  P. Corona,et al.  Influence of forest stand characteristics on physical, mechanical properties and chemistry of chestnut wood , 2021, Scientific Reports.

[6]  Y. Yamakoshi,et al.  Application of the novel estimation method by shear wave elastography using vibrator to human skeletal muscle , 2020, Scientific Reports.

[7]  M. Stoffel,et al.  Fire-scarred fossil tree from the Late Triassic shows a pre-fire drought signal , 2020, Scientific Reports.

[8]  Julie K. Nguyen,et al.  The genomic architecture of sex determining region and sex-related metabolic variation in Ginkgo biloba. , 2020, The Plant journal : for cell and molecular biology.

[9]  P. Mania,et al.  Acoustic Properties of Resonant Spruce Wood Modified Using Oil-Heat Treatment (OHT) , 2020, Materials.

[10]  Qinhui Zhang,et al.  Comprehensive assessment of growth traits and wood properties in half-sib Pinus koraiensis families , 2018, Euphytica.

[11]  Cranos M. Williams,et al.  Improving wood properties for wood utilization through multi-omics integration in lignin biosynthesis , 2018, Nature Communications.

[12]  P. David,et al.  Sex-specific strategies of resource allocation in response to competition for light in a dioecious plant , 2017, Oecologia.

[13]  B. Fei,et al.  Investigation of the multilayered structure and microfibril angle of different types of bamboo cell walls at the micro/nano level using a LC-PolScope imaging system , 2017, Cellulose.

[14]  Timothy K Lee,et al.  Rapid, precise quantification of bacterial cellular dimensions across a genomic-scale knockout library , 2017, BMC Biology.

[15]  T. Yin,et al.  Gender effects on Salix suchowensis Cheng ex Zhu. growth and wood properties as revealed by a full-sib pedigree , 2017, Canadian Journal of Plant Science.

[16]  Yaqiong Wu,et al.  The Effects of Fertilization on the Growth and Physiological Characteristics of Ginkgo biloba L. , 2016 .

[17]  Tao Wang,et al.  Gender-related differences in adaptability to drought stress in the dioecious tree Ginkgo biloba , 2016, Acta Physiologiae Plantarum.

[18]  A. García‐Cervigón,et al.  Intra-annual wood density fluctuations and tree-ring width patterns are sex- and site-dependent in the dioecious conifer Juniperus thurifera L. , 2015, Trees.

[19]  K. Nissinen,et al.  Sex-related differences in growth and carbon allocation to defence in Populus tremula as explained by current plant defence theories. , 2014, Tree physiology.

[20]  J. Caspersen,et al.  Quantifying the influence of live crown ratio on the mechanical properties of clear wood , 2013 .

[21]  S. Rood,et al.  Hydrologic linkages between a climate oscillation, river flows, growth, and wood Δ13C of male and female cottonwood trees. , 2013, Plant, cell & environment.

[22]  Helena Pereira,et al.  Estimation of Wood Basic Density of Acacia Melanoxylon (R. Br.) by near Infrared Spectroscopy , 2012 .

[23]  Zhaohua Lu,et al.  Genotypic variation in wood properties and growth traits of Eucalyptus hybrid clones in southern China , 2011, New Forests.

[24]  S. Mansfield,et al.  In situ wood quality assessment in Douglas-fir , 2011, Tree Genetics & Genomes.

[25]  W. Vermerris,et al.  Phenotypic plasticity in cell walls of maize brown midrib mutants is limited by lignin composition , 2010, Journal of experimental botany.

[26]  R. Dirzo,et al.  Sex-Related Differences in Reproductive Allocation, Growth, Defense and Herbivory in Three Dioecious Neotropical Palms , 2010, PloS one.

[27]  Qian Li,et al.  Development and application of SCAR markers for sex identification in the dioecious species Ginkgo biloba L. , 2009, Euphytica.

[28]  Stephan Getzin,et al.  Asymmetric tree growth at the stand level: Random crown patterns and the response to slope , 2007 .

[29]  G. R. Johnson,et al.  Genetic variation in basic density and modulus of elasticity of coastal Douglas-fir , 2006, Tree Genetics & Genomes.

[30]  P. D. Jones,et al.  Non-destructive estimation of Pinus taeda L tracheid morphological characteristics for samples from a wide range of sites in Georgia , 2005, Wood Science and Technology.

[31]  J. Oddershede,et al.  On the determination of crystallinity and cellulose content in plant fibres , 2005 .

[32]  A. E. Zavadskii X-ray diffraction method of determining the degree of crystallinity of cellulose materials of different anisotropy , 2004 .

[33]  J. R. Barnett,et al.  Cellulose microfibril angle in the cell wall of wood fibres , 2004, Biological reviews of the Cambridge Philosophical Society.

[34]  J. Obeso,et al.  The costs of reproduction in plants. , 2002, The New phytologist.

[35]  T. Gauquelin,et al.  Sex ratio and sexual dimorphism in mountain dioecious thuriferous juniper (Juniperus thurifera L., Cupressaceae) , 2002 .

[36]  M. C. Díaz Barradas,et al.  Ecophysiological differences between male and female plants of Pistacia lentiscus L. , 2000, Plant Ecology.

[37]  Chung-Jui Tsai,et al.  Repression of lignin biosynthesis promotes cellulose accumulation and growth in transgenic trees , 1999, Nature Biotechnology.

[38]  Tetsuo Kondo,et al.  FT-IR Microscopic Analysis of Changing Cellulose Crystalline Structure during Wood Cell Wall Formation , 1998 .

[39]  R. Durand,et al.  Sexual differentiation in higher plants , 1984 .

[40]  R. Savidge The role of plant hormones in higher plant cellular differentiation. II. Experiments with the vascular cambium, and sclereid and tracheid differentiation in the pine,Pinus contorta , 1983, The Histochemical Journal.

[41]  G. L. Franklin Preparation of Thin Sections of Synthetic Resins and Wood-Resin Composites, and a New Macerating Method for Wood , 1945, Nature.

[42]  Cedric E. Ginestet ggplot2: Elegant Graphics for Data Analysis , 2011 .

[43]  Philippe Rozenberg,et al.  Can wood density be efficiently selected at early stage in maritime pine (Pinus pinaster Ait.)? , 2011, Annals of Forest Science.

[44]  L. Zhenlin,et al.  Comparative anatomy of vessel elements in staminate and pistillate plants of Fraxinus pennsylvanica. , 2010 .