scholarly journals Prospects for dendroanatomy in paleoclimatology – a case study on Picea engelmannii from the Canadian Rockies

2022 ◽  
Author(s):  
Kristina Seftigen ◽  
Marina V. Fonti ◽  
Brian Luckman ◽  
Miloš Rydval ◽  
Petter Stridbeck ◽  
...  
Keyword(s):  
Cell Wall ◽  
Wall Thickness ◽  
Cell Wall Thickness ◽  
Picea Engelmannii ◽  
Potential Contribution ◽  
X Ray ◽  
Age Cohorts ◽  
Radial Cell ◽  
Radial Cell Wall

Abstract. The continuous development of new proxies as well as a refinement of existing tools are key to advances in paleoclimate research and improvements in the accuracy of existing climate reconstructions. Herein, we build on recent methodological progress in dendroanatomy – the analyses of wood anatomical parameters in dated tree rings – and introduce the longest (1585–2014 CE) dendroanatomical dataset currently developed for North America. We explore the potential of dendroanatomy of high-elevation Engelmann spruce (Picea engelmannii) as a proxy of past temperatures by measuring anatomical cell dimensions of 15 living trees from the Columbia Icefield area. There, X-ray maximum latewood density (MXD) and its blue intensity counterpart (MXBI) have previously been measured, which allows comparing the different parameters. Our findings highlight anatomical MXD and maximum radial cell wall thickness as the two most promising wood anatomical proxy parameters for past temperatures, each explaining 46 % and 49 %, respectively, of instrumental, high-pass filtered, July–August maximum temperatures over the 1901–1994 period. While both parameters display comparable climatic imprinting at higher frequencies to X-ray derived MXD, the anatomical dataset distinguishes itself from its predecessors by providing the most temporally stable warm-season temperature signal. For the long-term secular trends, discrepancies between anatomical MXD and maximum radial cell wall thickness chronologies were observed, where the former more closely follow the long-term variations of the X-ray based MXD. Further studies, including samples from more diverse age cohorts and the adaptation of RCS-based standardizations, are needed to disentangle the ontogenetic and climatic components of long-term signals stored in the wood anatomical traits and to more comprehensively evaluate the potential contribution of this new dataset to paleoclimate research.

scholarly journals Microstructure of chemically modified wood using X-ray computed tomography in relation to wetting properties

Holzforschung ◽  
2017 ◽  
Vol 71 (2) ◽  
pp. 119-128 ◽  
Author(s):  
Maziar Sedighi Moghaddam ◽  
Jan Van den Bulcke ◽  
Magnus E.P. Wålinder ◽  
Per M. Claesson ◽  
Joris Van Acker ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Cell Wall ◽  
Wall Thickness ◽  
Total Porosity ◽  
Cell Wall Thickness ◽  
X Ray ◽  
Wetting Properties ◽  
Vessel Elements ◽  
Capillary Uptake ◽  
X Ray Computed

Abstract X-ray computed tomography (XCT) was utilized to visualize and quantify the 2D and 3D microstructure of acetylated southern yellow pine (pine) and maple, as well as furfurylated pine samples. The total porosity and the porosity of different cell types, as well as cell wall thickness and maximum opening of tracheid lumens were evaluated. The wetting properties (swelling and capillary uptake) were related to these microstructural characteristics. The data show significant changes in the wood structure for furfurylated pine sapwood samples, including a change in tracheid shape and filling of tracheids by furan polymer. In contrast, no such changes were noted for the acetylated pine samples at the high resolution of 0.8 μm. The XCT images obtained for the furfurylated maple samples demonstrated that all ray cells and some vessel elements were filled with furan polymer while the fibers largely remained unchanged. Furfurylation significantly decreased the total porosity of both the maple and pine samples. Furthermore, this was observed in both earlywood (EW) and latewood (LW) regions in the pine samples. In contrast, the total porosity of pine samples was hardly affected by acetylation. These findings are in line with wetting results demonstrating that furfurylation reduces both swelling and capillary uptake in contrast to acetylation which reduces mostly swelling. Furfurylation significantly increased the cell wall thickness of both the maple and pine samples, especially at higher levels of furfurylation.

Properties of Gliricidia Wood (Gliricidia sepium) lntercropped with Cocoa (Theobroma cocoa) in Malaysia

2014 ◽  
Vol 11 (1) ◽  
pp. 51
Author(s):  
Mohd Helmy Ibrahim ◽  
Mohd Nazip Suratman ◽  
Razali Abd Kader
Keyword(s):  
Cell Wall ◽  
Specific Gravity ◽  
Moisture Content ◽  
Wall Thickness ◽  
Age Groups ◽  
Gliricidia Sepium ◽  
Cell Wall Thickness ◽  
Tree Age ◽  
Lumen Diameter ◽  
Significant Difference

Trees planted from agroforestry practices can become valuable resources in meeting the wood requirements of many nations. Gliricidia sepium is an exotic species introduced to the agricultural sector in Malaysia mainly for providing shade for cocoa and coffee plantations. This study investigates its wood physical properties (specific gravity and moisture content) and fibre morphology (length, lumen diameter and cell wall thickness) of G. sepium at three intervals according to age groups ( three, five and seven years of ages). Specific gravity (0.72) was significantly higher at seven years ofage as compared to five (0.41) and three (0.35) years age group with a mean of 0.43 (p<0.05). Mean moisture content was 58.3% with no significant difference existing between the tree age groups. Fibre diameter (22.4 mm) was significantly lower (p<0.05) for the trees which were three years of age when compared to five and seven years age groups (26.6 mm and 24. 7 mm), respectively. Means of fibre length, lumen diameter and cell wall thickness were 0.83 mm, 18.3 mm, and 6.2 mm, respectively, with no significant differences detected between trees in all age groups. Further calculation on the coefficient of suppleness and runkel ratio suggest that wood from G.sepium may have the potential for insulation board manufacturing and paper making. However, future studies should experiment the utilisation of this species for these products to determine its full potential.

Characterization of microstructures of SAN foam core using micro-computed tomography

2021 ◽  
pp. 026248932110068
Author(s):  
Youming Chen ◽  
Raj Das ◽  
Hui Wang ◽  
Mark Battley
Keyword(s):  
Cell Wall ◽  
Cell Size ◽  
Wall Thickness ◽  
Strain Localization ◽  
Cell Wall Thickness ◽  
Micro Computed Tomography ◽  
Average Cell Size ◽  
Average Cell ◽  
3D Images ◽  
Compressive Tests

In this study, the microstructure of a SAN foam was imaged using a micro-CT scanner. Through image processing and analysis, variations in density, cell wall thickness and cell size in the foam were quantitatively explored. It is found that cells in the foam are not elongated in the thickness (or rise) direction of foam sheets, but rather equiaxed. Cell walls in the foam are significantly straight. Density, cell size and cell wall thickness all vary along the thickness direction of foam sheets. The low density in the vicinity of one face of foam sheets leads to low compressive stiffness and strength, resulting in the strain localization observed in our previous compressive tests. For M80, large open cells on the top face of foam sheets are likely to buckle in compressive tests, therefore being another potential contributor to the strain localization as well. The average cell wall thickness measured from 2D slice images is around 1.4 times that measured from 3D images, and the average cell size measured from 2D slice images is about 13.8% smaller than that measured from 3D images. The dispersions of cell wall thickness measured from 2D slice images are 1.16–1.20 times those measured from 3D images. The dispersions of cell size measured from 2D slice images are 1.12–1.36 times those measured from 3D images.

Summer temperature in northeastern Siberia since 1642 reconstructed from tracheid dimensions and cell numbers of Larix cajanderi

2003 ◽  
Vol 33 (10) ◽  
pp. 1905-1914 ◽  
Author(s):  
Irina P Panyushkina ◽  
Malcolm K Hughes ◽  
Eugene A Vaganov ◽  
Martin AR Munro
Keyword(s):  
Cell Wall ◽  
Wall Thickness ◽  
Cell Number ◽  
Cell Wall Thickness ◽  
Cell Dimension ◽  
Cell Numbers ◽  
Age Related ◽  
Cambial Age ◽  
Northeastern Siberia ◽  
Larix Cajanderi

We reconstructed air temperature for two periods in the growth season from cell dimension and cell number variability in cross-dated tree rings of Larix cajanderi Mayr. from northeastern Siberia. Thirteen tree-ring chronologies based on cell size, cell wall thickness, and cell number were developed for AD 1642–1993. No clear evidence was found of an age-related trend in cell dimensions in the sampled materials, but cell numbers were correlated with cambial age. The chronologies contain strong temperature signals associated with the timing of xylem growth. We obtained reliable reconstructions of mean June temperature from the total cell number and July–September temperature from the cell wall thickness of latewood. June temperature and July–September temperature covaried for most of the period from AD 1642 to AD 1978. After that time, June temperature became cooler relative to July–September temperature. This difference caused disproportional changes in earlywood tracheids because of the late start of growth and cool conditions in June followed by warming during the rest of the season. The identification of this unusual recent change has shown that intraseasonal resolution may be achieved by cell dimension and cell number chronologies.

Variation in xylem anatomy of selected populations of lodgepole pine

2001 ◽  
Vol 31 (11) ◽  
pp. 2049-2057 ◽  
Author(s):  
Tongli Wang ◽  
Sally N Aitken
Keyword(s):  
Cell Wall ◽  
Wall Thickness ◽  
Slow Growth ◽  
Lodgepole Pine ◽  
High Density ◽  
Cell Wall Thickness ◽  
Fast Growth ◽  
Low Density ◽  
Xylem Anatomy ◽  
Latewood Density

Variation in xylem anatomy among selected populations of lodgepole pine (Pinus contorta Dougl. ex Loud. var. latifolia Engelm.) was examined using digital image analysis based on an annual growth ring (age 10) per tree. Four subpopulations were selected using the following criteria for height growth and wood density: (i) fast growth and high density; (ii) slow growth and high density; (iii) fast growth and low density; and (iv) slow growth and low density. Significant differences were found among subpopulations for several anatomical parameters including tracheid density, lumen size, and cell wall thickness that may affect the economic value and utilization of wood. Principal component analysis indicate that the first four principal components (PCs) were associated with (i) ring area (PC1), (ii) earlywood density (PC2), (iii) latewood density (PC3), and (iv) lumen shape in earlywood (PC4), suggesting that these aspects of wood properties and growth are controlled by different sets of genes. Relative contributions of total number of tracheids, tracheid lumen size, and cell wall thickness to ring area and correlations between cell wall area proportion and X-ray density are discussed.

scholarly journals Host Barriers and Responses to Uncinula necator in Developing Grape Berries

2004 ◽  
Vol 94 (5) ◽  
pp. 438-445 ◽  
Author(s):  
Andrea Ficke ◽  
David M. Gadoury ◽  
Robert C. Seem ◽  
Dale Godfrey ◽  
Ian B. Dry
Keyword(s):  
Cell Wall ◽  
Powdery Mildew ◽  
Wall Thickness ◽  
Infection Process ◽  
Cell Wall Thickness ◽  
Antifungal Compound ◽  
Uncinula Necator ◽  
Grape Berries ◽  
Pathogenesis Related ◽  
Cuticle Thickness

Grape berries are highly susceptible to powdery mildew 1 week after bloom but acquire ontogenic resistance 2 to 3 weeks later. We recently demonstrated that germinating conidia of the grape powdery mildew pathogen (Uncinula necator) cease development before penetration of the cuticle on older resistant berries. The mechanism that halts U. necator at that particular stage was not known. Several previous studies investigated potential host barriers or cell responses to powdery mildew in berries and leaves, but none included observation of the direct effect of these factors on pathogen development. We found that cuticle thickness increased with berry age, but that ingress by the pathogen halted before formation of a visible penetration pore. Cell wall thickness remained unchanged over the first 4 weeks after bloom, the time during which berries progressed from highly susceptible to nearly immune. Autofluorescent polyphenolic compounds accumulated at a higher frequency beneath appressoria on highly susceptible berries than on highly resistant berries; and oxidation of the above phenolics, indicated by cell discoloration, developed at a significantly higher frequency on susceptible berries. Beneath the first-formed appressoria of all germinated conidia, papillae occurred at a significantly higher frequency on 2- to 5-day-old berries than on 30- to 31-day-old fruit. The relatively few papillae observed on older berries were, in most cases (82.8 to 97.3%), found beneath appressoria of conidia that had failed to produce secondary hyphae. This contrasted with the more abundantly produced papillae on younger berries, where only 35.4 to 41.0% were located beneath appressoria of conidia that had failed to produce secondary hyphae. A pathogenesis-related gene (VvPR-1) was much more highly induced in susceptible berries than in resistant berries after inoculation with U. necator. In contrast, a germin-like protein (VvGLP3) was expressed within 16 h of inoculation in resistant, but not in susceptible berries. Our results suggest that several putative barriers to infection, i.e., cuticle and cell wall thickness, antimicrobial phenolics, and two previously described pathogenesis-related proteins, are not principal causes in halting pathogen ingress on ontogenically resistant berries, but rather that infection is halted by one or more of the following: (i) a preformed physical or biochemical barrier near the cuticle surface, or (ii) the rapid synthesis of an antifungal compound in older berries during the first few hours of the infection process.

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