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Fibre wall and lumen fractions drive wood density variation across 24 Australian angiosperms

ABSTRACT: Wood density is often considered to be a key plant functional trait. But it is not clear what actually wood density is? We rigorously quantified anatomical underpinnings of wood density variation. We found that density was mainly driven by properties of mechanical tissue such as fibre wall fraction and fibre lumen fraction. However, there was also a substantial anatomical variation independent of density. This variation suggests that different plant ecological strategies may be available to woods with the same density. Our results imply that density is a complex characteristic of wood rather than a straightforward indicator of plant ecological strategies. Wood density is considered a key plant trait, affecting mechanical and physiological performance, yet its biological meaning is still rather unclear. Accordingly we investigated the anatomical underpinnings of wood density in trees and shrubs. We measured wood density and anatomical traits in distal stems 4–10 mm diameter under bark in 24 Australian species. Proportions of wood components that are functionally distinct were analysed, including fibre wall and lumen, vessel wall and lumen, and axial and ray parenchyma. Wood density was mainly driven by the density of wood outside vessel lumens (densityNV) rather than by vessel lumen fraction. In turn, densityNV variation was chiefly affected by fibre wall and lumen fractions. Considerable anatomical variation was observed at a given densityNV, especially among medium-densityNV species (0.60–0.85 g cm?3); this range of medium densityNV roughly translates to 0.50–0.75 g cm?3 of overall density. The anatomy of these species formed a continuum from low fibre lumen and medium parenchyma fractions to medium fibre lumen and low parenchyma fractions. Our data suggest that wood density is an emergent property influenced by a complex anatomy rather than an unambiguous functional trait, particularly in medium-density species. With much anatomical variation, they likely represent a wide range of ecological strategies.

SUBMITTER: Zieminska K

PROVIDER: S-EPMC4104653 | biostudies-literature | 2013 Jan

REPOSITORIES: biostudies-literature

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Project description:BackgroundFlow-mediated dilation (FMD) and carotid intima-medial thickness (CIMT), measured by ultrasound, are widely used to test the efficacy of cardioprotective interventions. Although assessment methods vary, automated edge-detecting image analysis software is routinely used to measure changes in FMD and CIMT. We aimed to quantify the effect that commonly adjusted ultrasound settings have on arterial lumen and wall thickness measurements made with CIMT measurement software.MethodsWe constructed phantom arteries from a tissue-mimicking agar compound and scanned them in a water bath with a 10 MHz multi-frequency linear-array probe attached to a high-resolution ultrasound machine. B-mode images of the phantoms were recorded with dynamic range (DR) and gain set at five decibel (dB) increments from 40 dB to 60 dB and -10 dB to +10 dB respectively. Lumen diameter and wall-thickness were measured off-line using CIMT measurement software.ResultsLumen measurements: there was a strong linear relationship between DR and gain and measured lumen diameter. For a given gain level, a 5 dB increase in DR reduced the measured lumen diameter by 0.02 +/- 0.004 mm (p < 0.001). For a given DR level, a 5 dB increase in gain reduced measured lumen diameter by 0.04 +/- 0.004 mm (p < 0.001). A 5 mm increase in distance between the ultrasound probe and the artery reduced measured lumen diameter by 0.04 +/- 0.03 mm (p < 0.001)CIMT measurements: For a fixed gain level, a 5 dB increase in DR increased measured wall thickness by 0.003 +/- 0.002 mm (p < 0.001). The effects of increasing gain were not consistent and appeared to vary depending on the distance between the artery and the ultrasound probe and the thickness of the artery wall.ConclusionDR, gain and probe distance significantly alter lumen diameter and CIMT measurements made using image analysis software. When CIMT and FMD are used to test the efficacy of cardioprotective interventions, the DR, gain and probe position used to record baseline scans should be documented and replicated in post-treatment scans in individual trial subjects. If more than one sonographer or imaging centre is used to collect data, the study protocol should document specific DR and gain settings to be used in all subjects.

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Fibre wall and lumen fractions drive wood density variation across 24 Australian angiosperms

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