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Growth and wood quality of plantation grown Eucalyptus dunnii

Growth and wood quality of plantation grown Eucalyptus dunnii

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<strong>Growth</strong> <strong>and</strong> <strong>wood</strong> <strong>quality</strong> <strong>of</strong> <strong>plantation</strong> <strong>grown</strong> <strong>Eucalyptus</strong> <strong>dunnii</strong><br />

Dane Thomas 1 , Michael Henson 1 , Bill Joe 2 , Steve Boyton 1 , Ross Dickson 2<br />

1 Forests NSW, L<strong>and</strong> Management <strong>and</strong> Technical Services, C<strong>of</strong>fs Harbour, NSW, Australia<br />

2 Forests NSW, L<strong>and</strong> Management <strong>and</strong> Technical Services, West Pennant Hills, Sydney, NSW,<br />

Australia<br />

Forests NSW manages <strong>Eucalyptus</strong> <strong>plantation</strong>s on the north coast <strong>of</strong> NSW, Australia for high value<br />

timber production. Productivity, <strong>wood</strong> properties <strong>and</strong> mill recovery <strong>of</strong> <strong>Eucalyptus</strong> <strong>dunnii</strong> Maiden, a<br />

species becoming increasingly important to eucalypt hard<strong>wood</strong> producers worldwide was investigated.<br />

Historic data from st<strong>and</strong>s aged from 3 to 34 years were assessed for growth, <strong>and</strong> <strong>wood</strong> <strong>quality</strong> using a<br />

range <strong>of</strong> non-destructive <strong>and</strong> destructive measurements. These measurements were analysed to<br />

determine <strong>wood</strong> properties that may influence grade yield. Many <strong>wood</strong> <strong>quality</strong> traits could be<br />

correlated with basic density, which was correlated with tree age. This has implications for the timber<br />

industry as it is intended that <strong>plantation</strong> trees will be harvested at younger ages than native forest trees.<br />

The predictive ability <strong>of</strong> these models will be tested shortly when E. <strong>dunnii</strong> <strong>of</strong> three different ages –<br />

12, 16 <strong>and</strong> 34 – years will be harvested <strong>and</strong> pulp, sawlog <strong>and</strong> veneer recovery assessed.<br />

Keywords<br />

Dunn’s white gum, <strong>Eucalyptus</strong> <strong>dunnii</strong>, eucalypt, janka hardness, MOE, MOR, shrinkage<br />

Paper<br />

<strong>Eucalyptus</strong> <strong>dunnii</strong> Maiden (Dunn’s white gum) naturally occurs in two small disjunct populations on<br />

north eastern NSW <strong>and</strong> south eastern Queensl<strong>and</strong> primarily on the margins <strong>of</strong> rainforests (Bol<strong>and</strong> et<br />

al., 2006). These sites have a summer rainfall pattern with 1100-1500 mm mean annual rainfall, <strong>and</strong><br />

are typically fertile basaltic or alluvial soils between 400 m <strong>and</strong> 650 m altitude (Benson <strong>and</strong> Hager,<br />

1993). <strong>Eucalyptus</strong> <strong>dunnii</strong> has recently gained favour as an alternative <strong>plantation</strong> species to E. gr<strong>and</strong>is<br />

because it is more suited drier <strong>and</strong>/or more frost prone sites (Darrow, 1994; Johnston <strong>and</strong> Arnold,<br />

2000). This has lead to its establishment mostly on higher altitude sites (>500 m asl), or on lower–<br />

lying creek flats prone to frost. In NSW, Forests NSW has established over 8,500 ha, with the vast<br />

majority <strong>of</strong> these <strong>plantation</strong>s being established since 1994.<br />

<strong>Growth</strong><br />

Several trials are available to evaluate growth <strong>of</strong> E. <strong>dunnii</strong>. Five species trials planted in NSW from<br />

1972 to 1976 at Bulahdelah(Lat 32° 24’S Long. 152° 15’E), Cascade (Lat 30° 13’S Long. 152° 46’E),<br />

Chichester (Lat 32° 14’S Long. 151° 46’E), Yabbra (Lat 28° 32’S Long. 152° 34’E), Watagan (Lat<br />

33° 03’S Long. 151° 20’E) on a range <strong>of</strong> soil types, climate <strong>and</strong> local within-site environments are<br />

useful to compare the performance <strong>of</strong> E. <strong>dunnii</strong> with either E. pilularis or E. gr<strong>and</strong>is or both (Johnson<br />

<strong>and</strong> Stanton, 1993). These latter species are compared to demonstrate the potential uses <strong>of</strong> E. <strong>dunnii</strong><br />

as an alternative to E. gr<strong>and</strong>is for pulp production, <strong>and</strong> an alternative to E. pilularis for solid <strong>wood</strong> or<br />

veneer production. Figure 1 shows diameter over bark at 1.3m (DBH) <strong>and</strong> tree height were<br />

comparable between the three species within a site for the five sites signifying that E. <strong>dunnii</strong> performs<br />

as well as an alternate species, although site effects existed for all species. <strong>Growth</strong> <strong>of</strong> 9 <strong>and</strong> 14 year<br />

old E. <strong>dunnii</strong> in Argentina were comparable to these reported values (Marco <strong>and</strong> Lopez, 1995). This<br />

figure also shows growth over time for E. <strong>dunnii</strong> growing at Cascade <strong>and</strong> Chichester, two <strong>of</strong> the<br />

unthinned species trials planted in 1973, <strong>and</strong> growth at two progeny trials located at Boambee (Lat 30°<br />

18’S Long. 153° 03’E), <strong>and</strong> Megan (Lat 30° 17’S Long. 152° 47’E), planted in 1995. These data<br />

show growth at the two progeny trials is similar to the earlier planted species trials, although site<br />

effects are noticeable. Both sites have yellow podzolic soils although Boambee is a higher <strong>quality</strong> site<br />

with predicted MAI at 20 years <strong>of</strong> 20 m 3 ha -1 compared to 15 m 3 ha -1 at Megan (Henson <strong>and</strong> Vanclay,<br />

2004), Boambee also has lower mean elevation, higher mean minimum temperatures, <strong>and</strong> slightly


higher rainfall than Megan. The Boambee <strong>and</strong> Megan progeny trials were thinned from 1388 s.p.h. to<br />

694 at age 4.5 year. The Boambee progeny trial is due to be thinned to 347 s.p.h. later this year.<br />

Despite the acceptable growth performance <strong>of</strong> E. <strong>dunnii</strong> measured as diameter, height, or volume this<br />

‘growth’ is only one attribute <strong>of</strong> timber. The end use <strong>of</strong> the timber also has to be considered. The<br />

Boambee trial will be used to assess solid, veneer <strong>and</strong> pulp <strong>wood</strong> properties <strong>of</strong> this high performing<br />

younger st<strong>and</strong> at age 12 years. Two other sites aged 16 <strong>and</strong> 34 years will also be harvested <strong>and</strong> similar<br />

end uses evaluated. Non-destructive measurements associated with <strong>wood</strong> <strong>quality</strong> traits have been<br />

evaluated on these trials at earlier ages.<br />

Diameter breast height (cm)<br />

Tree height (m)<br />

40<br />

35<br />

30<br />

25<br />

20<br />

15<br />

10<br />

5<br />

0<br />

40<br />

35<br />

30<br />

25<br />

20<br />

15<br />

10<br />

5<br />

0<br />

0 5 10 15 20 25 30 35<br />

Age (years)<br />

0 5 10 15 20 25 30 35<br />

Age (years)<br />

E. <strong>dunnii</strong><br />

E. gr<strong>and</strong>is<br />

E. pilularis<br />

Cascade<br />

Chichester<br />

Boambee<br />

Megan<br />

E. <strong>dunnii</strong><br />

E. gr<strong>and</strong>is<br />

E. pilularis<br />

Cascade<br />

Chichester<br />

Boambee<br />

Megan<br />

Figure 1. Mean diameter over bark at 1.3m (DBH) <strong>and</strong> mean tree height at last formal measurement <strong>of</strong> E.<br />

<strong>dunnii</strong> (open square), E. gr<strong>and</strong>is (open triangle) <strong>and</strong> E. pilularis (open circle) from 5 ‘species’ trials. Mean<br />

tree growth <strong>of</strong> E. <strong>dunnii</strong> over time for two <strong>of</strong> these trials at Cascade (solid square) <strong>and</strong> Chichester (solid<br />

diamond) are shown. Additionally mean growth at two E. <strong>dunnii</strong> progeny trials at Boambee (solid triangle)<br />

<strong>and</strong> Megan (solid circle) are shown.<br />

Density<br />

Wood density is <strong>of</strong>ten used to characterise <strong>wood</strong> because it is correlated, although perhaps not always<br />

causally related, with many <strong>quality</strong> traits. Denser <strong>wood</strong> tends to be stronger but may have higher<br />

shrinkage <strong>and</strong> more checks in dried <strong>wood</strong>. Denser <strong>wood</strong> contains more <strong>wood</strong> per unit volume thus it


tends to give higher yield <strong>of</strong> pulp in paper manufacturing. Thus information about <strong>wood</strong> density is<br />

useful to <strong>plantation</strong> management.<br />

Density typically increases with tree age as the proportion <strong>of</strong> lower density material formed early in<br />

the trees life is reduced by the higher density material formed in older trees (eg. de Silva et al., 2004).<br />

Basic density <strong>of</strong> native forest E. <strong>dunnii</strong> is reported to be 610 kg m -3 (Bootle, 2005). These data are<br />

probably from mature native forest st<strong>and</strong>s. Data from a combination <strong>of</strong> basic density <strong>of</strong> 12 mm<br />

diametric (bark to bark) cores, whole disks at DBH, <strong>and</strong> estimation <strong>of</strong> whole tree density were used to<br />

develop a relationship with tree age for NSW <strong>plantation</strong> material. Density <strong>of</strong> <strong>plantation</strong> <strong>grown</strong><br />

material from NSW <strong>and</strong> elsewhere shows there is a trend <strong>of</strong> increasing basic density in older trees to<br />

approximately 600 kg m -3 at 25 years although there is some variability with method <strong>of</strong> sampling<br />

<strong>and</strong>/or site with non NSW sites (predominantly South American) (Ribeiro <strong>and</strong> Filho, 1993, Marco <strong>and</strong><br />

Lopez, 1995; Calori <strong>and</strong> Kikuti, 1997; Ferriera et al., 1997; Backman <strong>and</strong> deLeon, 1998; Dickson et<br />

al., 2003; Arnold et al., 2004; Henson et al., 2004; Muneri et al., 2007) (Figure 2). Mature native<br />

forest tree age was assumed to be 34 years (although is probably older) for no other reason but to<br />

graphically present the data provided by Bootle (2005). The relationship between tree age <strong>and</strong> density<br />

<strong>of</strong> NSW <strong>plantation</strong> E. <strong>dunnii</strong> had a high correlation coefficient <strong>of</strong> 0.91, n=9.<br />

Density can be “predicted” non-destructively from pilodyn penetration. Relationships between pilodyn<br />

<strong>and</strong> density <strong>of</strong> whole tree <strong>and</strong> <strong>wood</strong> disk at breast height were developed for NSW <strong>plantation</strong>s. A<br />

relationship with whole tree density was developed from two sites aged 8 years using 4 pilodyn<br />

measurements per tree at breast height <strong>and</strong> whole tree density averaged from 6 disks collected at<br />

heights ranging from 0.3 m to 90% tree height (Henson, unpublished data). A further relationship was<br />

developed for density <strong>of</strong> a <strong>wood</strong> disk at breast height from 9 year data collected at one site using 47<br />

family mean values <strong>of</strong> one pilodyn reading per tree <strong>and</strong> an average <strong>of</strong> 4 trees per family. These<br />

relationships allowed predictions <strong>of</strong> basic density <strong>of</strong> NSW <strong>plantation</strong>s aged 11, 16 <strong>and</strong> 32 years to be<br />

540, 530 <strong>and</strong> 563 kg m -3 respectively. Predicted basic density at these ages show these E. <strong>dunnii</strong> are<br />

similar to other reported values <strong>and</strong> fall on the general age based relationship developed earlier (Figure<br />

2).<br />

Basic density (kg m-3)<br />

700<br />

600<br />

500<br />

400<br />

300<br />

200<br />

100<br />

0<br />

R 2 = 0.91 n=9<br />

0 5 10 15 20 25 30 35<br />

Age (years)<br />

Tree<br />

Disk<br />

Core<br />

Non NSW<br />

Predicted<br />

NSW<br />

Mature<br />

Log. (NSW)<br />

Figure 2. Basic density <strong>of</strong> E. <strong>dunnii</strong> as a function <strong>of</strong> tree age. NSW <strong>plantation</strong> data are shown in blue with<br />

density calculated from whole tree (solid diamond), calculated from disks (solid circle), <strong>wood</strong> cores (solid<br />

square). The regression relationship uses these data. Non-NSW data are shown as solid triangles. Density <strong>of</strong><br />

NSW <strong>plantation</strong>s aged 12, 16 <strong>and</strong> 32 years predicted using pilodyn relationships are shown as open circles.<br />

Density <strong>of</strong> mature native forest trees are shown as large solid circle, <strong>and</strong> an age <strong>of</strong> 34 years was selected for<br />

ease <strong>of</strong> graphic display.


Pulp characteristics<br />

Pulp characteristics <strong>of</strong> E. <strong>dunnii</strong> have been evaluated at age 8 years at Megan <strong>and</strong> Boambee, <strong>and</strong> at age<br />

9 years at Boambee. Boambee is a higher <strong>quality</strong> site than Megan resulting in approximately twice the<br />

height <strong>and</strong> diameter growth (Figure 1) <strong>and</strong> 4 times the volume growth at age 9. Boambee trees were<br />

easier to pulp, required 12.8% active alkali, produced 53% screened pulp <strong>and</strong> had a higher pulp yield<br />

<strong>of</strong> 277 kg m -3 compared to 13.8% active alkali, 50% screened pulp, <strong>and</strong> 237 kg m -3 pulp yield at<br />

Megan (Muneri et al., 2007). The Boambee results are comparable to both 9 year old E. <strong>dunnii</strong> <strong>grown</strong><br />

in South Africa (Clark <strong>and</strong> Hicks, 2003) <strong>and</strong> 4 year old trees <strong>grown</strong> in South America (Backman <strong>and</strong><br />

deLeon, 1998). The smaller fibre length at Megan <strong>of</strong> 0.74 mm was similar to the Clarks (1995)<br />

results, which were both shorter than the average fibre lengths <strong>of</strong> 0.86 mm at Boambee. These data<br />

show site <strong>quality</strong> can impact on pulp yield <strong>and</strong> <strong>quality</strong>. Silvicultural practices such as stocking can<br />

also impact on pulp productivity <strong>of</strong> E. <strong>dunnii</strong> (Ferreira et al., 1997) through, amongst other factors,<br />

changes in pulping characteristics, tree diameter <strong>and</strong> height growth, <strong>and</strong> <strong>wood</strong> density.<br />

Basic density <strong>and</strong> pulp yield <strong>of</strong> 8 year old E. <strong>dunnii</strong> growing at Boambee <strong>and</strong> Megan <strong>plantation</strong>s were<br />

recently estimated using Near Infrared spectroscopy (Muneri et al., 2004). This technique <strong>of</strong>fers fast<br />

cost effective evaluation <strong>of</strong> economic potential <strong>of</strong> trees. The predicted values were within 2% <strong>of</strong><br />

observed values, with high correlation coefficients. These relationships will be tested on other sites<br />

<strong>and</strong> older trees to determine the effectiveness <strong>of</strong> these relationships.<br />

Solid Wood<br />

<strong>Growth</strong> stresses<br />

Solid <strong>wood</strong> properties <strong>of</strong> E. <strong>dunnii</strong> are in many ways more difficult to ascertain than density or pulping<br />

characteristics. One common problem <strong>of</strong> <strong>plantation</strong>-<strong>grown</strong> <strong>wood</strong> as opposed to native forest sourced<br />

material is related to growth stresses. <strong>Growth</strong> stresses are little understood but are thought to be<br />

related to the growth rate <strong>of</strong> trees <strong>and</strong> <strong>of</strong>ten decline with tree age. Peripheral growth stresses in 9 year<br />

old E. <strong>dunnii</strong> <strong>grown</strong> at Boambee were evaluated recently (Murphy et al., 2005). <strong>Growth</strong> stresses were<br />

found to be heritable, but it was also observed that taller thinner trees had more growth stress than<br />

short thick trees (Murphy et al., 2005) suggesting stresses may be altered by site <strong>and</strong> silvicultural<br />

management influences on stem taper.<br />

<strong>Growth</strong> stresses are a major concern when processing timber. It has been estimated that one third <strong>of</strong><br />

sawn material from <strong>plantation</strong> <strong>grown</strong> E. <strong>dunnii</strong> may suffer degrade attributable to growth stress (Matos<br />

et al., 2003). Similar degrade was reported in 10 year old <strong>plantation</strong> <strong>grown</strong> E. globulus where 30% <strong>of</strong><br />

boards were ejected due to excessive distortion <strong>and</strong> 40% <strong>of</strong> this distortion could be attributed to<br />

growth stress (Yang et al., 2001, 2002). It is therefore not surprising that methods have been examined<br />

to reduce losses due to growth stress. Alternate sawing techniques are used to increase recoveries.<br />

Additionally various methods have been used to reduce <strong>and</strong> release growth stresses prior to harvest<br />

(Malan, 1995). Techniques such as girdling <strong>of</strong> st<strong>and</strong>ing trees, or partial defoliation prior to harvest<br />

were shown to reduce growth stresses <strong>of</strong> E. gr<strong>and</strong>is although the variation between trees <strong>and</strong> excessive<br />

decay <strong>of</strong> girdled trees was excessive (Malan, 1995). Herbicide <strong>and</strong> radial cuts were most effective in<br />

reducing growth stresses <strong>of</strong> E. <strong>dunnii</strong> (Matos et al., 2003). Post- harvest steaming treatments prior to<br />

milling were also effective in reducing splitting <strong>and</strong> other growth stress related defects in E. <strong>dunnii</strong><br />

(Severo <strong>and</strong> Tomaselli, 2000).<br />

Shrinkage <strong>and</strong> collapse<br />

Shrinkage <strong>of</strong> <strong>wood</strong> is a further <strong>quality</strong> attribute with some correlation with growth stress. Ten year<br />

old E. nitens with low growth stress had less shrinkage (Chauhan <strong>and</strong> Walker, 2004), while Yang <strong>and</strong><br />

Pongracic (2004) found a weak negative relationship between tangential shrinkage <strong>and</strong> growth stress<br />

<strong>of</strong> ten year old E. globulus. A strong relationship existed between growth stress <strong>and</strong> the difference in<br />

shrinkage between heart<strong>wood</strong> <strong>and</strong> sap<strong>wood</strong> <strong>of</strong> E. nitens (Chauhan <strong>and</strong> Walker, 2004). Shrinkage <strong>of</strong> E.<br />

globulus sap<strong>wood</strong> was typically low at about half that <strong>of</strong> outer heart<strong>wood</strong> (Yang <strong>and</strong> Pongracic, 2004).<br />

It is clear the relationship between growth stress <strong>and</strong> shrinkage requires further research.<br />

Bootle (2005) lists tangential shrinkage <strong>of</strong> mature native forest E. <strong>dunnii</strong> <strong>of</strong> an unknown age to be 10%<br />

<strong>and</strong> radial shrinkage at 5%, giving a ratio between tangential <strong>and</strong> radial shrinkage <strong>of</strong> 2.0. Lower<br />

shrinkage ratios are desirable as cupping <strong>of</strong> boards during drying would be reduced with more uniform


shrinkage ratios. Older <strong>plantation</strong> <strong>grown</strong> E. <strong>dunnii</strong> have comparable shrinkage to mature trees noted in<br />

Bootle (2005). Tangential shrinkage <strong>of</strong> 10.2% <strong>and</strong> radial shrinkage <strong>of</strong> 6.2% were found in 20 year old<br />

Brazilian <strong>plantation</strong> E. <strong>dunnii</strong>, giving a lower ratio between tangential shrinkage <strong>and</strong> radial shrinkage<br />

<strong>of</strong> almost 1.5 (Calori <strong>and</strong> Kikuti, 1997). Shrinkage after re-conditioning to recover collapse <strong>of</strong> 29<br />

year old E. <strong>dunnii</strong> at Chichester, NSW was 8.4% tangentially <strong>and</strong> 3.2% radially (Joe, unpublished<br />

data), while shrinkage after re-conditioning to recover collapse <strong>of</strong> 6 year old E. <strong>dunnii</strong> was 6.2%<br />

tangentially <strong>and</strong> 2.2% radially (Joe, unpublished data). These shrinkage values are less than the<br />

Brazilian trees, but in each case the ratio between tangential <strong>and</strong> radial shrinkage was higher at 2.6 for<br />

the 29 year material <strong>and</strong> 2.8 for the 6 year old material. Collapse in the NSW <strong>plantation</strong> material<br />

accounted for about 4% <strong>of</strong> the un-recovered tangential shrinkage but less than 1% <strong>of</strong> the radial<br />

shrinkage (Joe, unpublished). Recovery <strong>of</strong> this collapse could lead to checking <strong>and</strong> be detrimental to<br />

appearance grade products (Har<strong>wood</strong> et al., 2005).<br />

Shrinkage in 9 year old age <strong>plantation</strong>-<strong>grown</strong> E. <strong>dunnii</strong> from NSW has also been examined on 12 mm<br />

diametric (bark to bark) pseudo cores (B<strong>and</strong>ara, 2006). Tangential shrinkage was 7.1% while collapse<br />

was found to be 10% (B<strong>and</strong>ara, 2006). No data are available <strong>of</strong> radial variation in these shrinkage or<br />

collapse values. However, Henson et al., (2004) report tangential <strong>and</strong> radial shrinkage <strong>of</strong> boards<br />

obtained from this material <strong>and</strong> dried quickly to exacerbate distortion to be 11.7% <strong>and</strong> 3.1%<br />

respectively. This corresponds to a ratio <strong>of</strong> tangential to radial shrinkage <strong>of</strong> 3.8, a value higher than in<br />

other reports.<br />

The high ratio <strong>of</strong> tangential to radial shrinkage for NSW <strong>plantation</strong>s is <strong>of</strong> concern as sawn material<br />

will be under differential stresses while drying, which may lead to drying related defects such as<br />

cupping (Har<strong>wood</strong> et al., 2005). Har<strong>wood</strong> et al. (2005) <strong>and</strong> B<strong>and</strong>ara (2006) noted a high percentage<br />

<strong>of</strong> boards sawn from 9 year old material displayed cupping after drying. Following reconditioning<br />

27% <strong>of</strong> these boards had unrecoverable collapse (shrinkage) related defects on an average <strong>of</strong> 60% <strong>of</strong><br />

their length, while surface checking was visible on less than 0.1% <strong>of</strong> the board length (Har<strong>wood</strong> et al.<br />

2005; B<strong>and</strong>ara, 2006).<br />

It is interesting to note that the higher ratio <strong>of</strong> tangential to radial shrinkage in NSW <strong>plantation</strong><br />

material is different to both the older native forest resource <strong>and</strong> the 20 year old Brazilian <strong>plantation</strong><br />

material. This suggests this difference is not solely related to age <strong>of</strong> the material. The higher ratio in<br />

the NSW <strong>plantation</strong> material is due more to proportionally much lower radial shrinkage in the NSW<br />

<strong>plantation</strong> material than to differences in tangential shrinkage between the two sources <strong>of</strong> trees.<br />

Differential transverse shrinkage can be due to many factors including gross anatomical structures<br />

such as cell lumen size or cell wall thickness, or presence <strong>of</strong> <strong>wood</strong> rays, or more detailed structure<br />

such as cell wall micr<strong>of</strong>ibril angle, or composition <strong>of</strong> the middle lamella (Kollman <strong>and</strong> Cote, 1977).<br />

Clearly the higher ratio <strong>of</strong> tangential shrinkage to radial shrinkage <strong>of</strong> NSW <strong>plantation</strong> <strong>grown</strong> E. <strong>dunnii</strong><br />

needs to be addressed. Gains could be made through greater use <strong>of</strong> improved genetic material as it has<br />

been shown that <strong>wood</strong> traits are highly heritable, <strong>and</strong> that for E. pilularis tangential <strong>and</strong> radial<br />

shrinkage <strong>and</strong> their ratio is under genetic control (Pelletier, 2006; Henson Pers Comm).<br />

A simple regression between basic density <strong>and</strong> tangential shrinkage <strong>of</strong> mean values for the 3 NSW<br />

<strong>plantation</strong>-<strong>grown</strong> E. <strong>dunnii</strong> gave a positive relationship (Figure 3). This is not unexpected as others<br />

(eg. Kollman <strong>and</strong> Cote, 1977; West, 2006) have noted that the thicker cell walls <strong>of</strong> denser <strong>wood</strong> tend<br />

to contain larger amounts <strong>of</strong> water than cells <strong>of</strong> less dense <strong>wood</strong>, which makes denser <strong>wood</strong> subject to<br />

more shrinkage. The corresponding values for mature trees provided by Bootle (2005) agree with the<br />

correlation developed using NSW <strong>plantation</strong> <strong>grown</strong> E. <strong>dunnii</strong>.


Tangential shrinkage (%)<br />

12<br />

10<br />

8<br />

6<br />

4<br />

2<br />

R 2 = 0.9997 n=3<br />

0<br />

300 400 500 600 700<br />

Basic density (kg m-3)<br />

NSW<br />

Mature<br />

Non NSW<br />

Linear (NSW)<br />

Figure 3. Tangential shrinkage after re-conditioning <strong>of</strong> <strong>plantation</strong> <strong>grown</strong> E. <strong>dunnii</strong> as a function <strong>of</strong> basic<br />

density. Means <strong>of</strong> three experiments using NSW <strong>plantation</strong> material <strong>of</strong> different ages (solid square). The<br />

regression relationship uses these three data. Non-NSW data are shown as solid triangle. Mature native forest<br />

tree are shown as solid circle.<br />

Mechanical Properties<br />

Hardness, modulus <strong>of</strong> rupture (MOR) <strong>and</strong> modulus <strong>of</strong> elasticity (MOE) are the principal mechanical<br />

properties dictating uses <strong>of</strong> solid <strong>wood</strong>.<br />

Hardness<br />

Wood hardness is a measure <strong>of</strong> resistance to indentation, <strong>and</strong> provides an indication to how well the<br />

<strong>wood</strong> performs to wear <strong>and</strong> marking. It is an important <strong>quality</strong> trait for flooring <strong>and</strong> furniture, <strong>and</strong> is<br />

less important for other solid <strong>wood</strong> products. Phenotypic correlations between hardness <strong>and</strong> density <strong>of</strong><br />

eucalypts including E. <strong>dunnii</strong> have been shown to be positive (eg. Dickson et al., 2003). The<br />

regression <strong>of</strong> hardness <strong>and</strong> density, <strong>and</strong> hardness <strong>and</strong> tree age using site means <strong>of</strong> NSW <strong>plantation</strong><br />

<strong>grown</strong> E. <strong>dunnii</strong> were positive (Figure 4). Data from mature E. <strong>dunnii</strong> <strong>and</strong> E. <strong>dunnii</strong> <strong>grown</strong> in Brazil<br />

agree with these relationships, suggesting hardness will increase with <strong>plantation</strong> age because density<br />

will increase with <strong>plantation</strong> age. Predicted hardness for other NSW E. <strong>dunnii</strong> <strong>plantation</strong>s aged 12, 16<br />

<strong>and</strong> 32 years are shown. Basic densities <strong>of</strong> these trials were predicted from relationships between<br />

pilodyn <strong>and</strong> density.


Hardness<br />

Hardness<br />

8<br />

7<br />

6<br />

5<br />

4<br />

3<br />

2<br />

1<br />

0<br />

8<br />

7<br />

6<br />

5<br />

4<br />

3<br />

2<br />

1<br />

0<br />

R 2 = 0.90 n=5<br />

0 5 10 15 20 25 30 35<br />

Age (years)<br />

R 2 = 0.94 n=5<br />

300 400 500 600 700<br />

Basic density (kg m-3)<br />

NSW<br />

Mature<br />

Non NSW<br />

Predicted from Density<br />

Linear (NSW)<br />

NSW<br />

Mature<br />

Non NSW<br />

Predicted from Age<br />

Linear (NSW)<br />

Figure 4. Hardness <strong>of</strong> E. <strong>dunnii</strong> as a function <strong>of</strong> basic density <strong>and</strong> <strong>of</strong> age. NSW <strong>plantation</strong> material are shown<br />

as solid square <strong>and</strong> the regression equation was calculated using these data. Non-NSW data are shown as<br />

solid triangle. Mature native forest tree are shown as large solid circle, <strong>and</strong> an age <strong>of</strong> 34 years was selected<br />

for ease <strong>of</strong> graphic display. Hardness predicted for 3 <strong>plantation</strong>s using the relationship with density are shown<br />

as open circles, while hardness predicted from the relationship with <strong>plantation</strong> age are shown by open squares.<br />

Modulus <strong>of</strong> Rupture, Modulus <strong>of</strong> Elasticity<br />

Modulus <strong>of</strong> rupture was found to be related to density <strong>and</strong> to age in <strong>plantation</strong>-<strong>grown</strong> E. <strong>dunnii</strong> (Figure<br />

5). Both relationships were positive with correlation coefficients greater than 0.9 for the relationship<br />

with basic density <strong>and</strong> 0.67 for the relationship with tree age. The data for mature native forest<br />

sourced E. <strong>dunnii</strong> was similar to experimental data (Bootle, 2005).


MOR (MPa)<br />

MOR (MPa)<br />

160<br />

140<br />

120<br />

100<br />

80<br />

60<br />

40<br />

20<br />

0<br />

160<br />

140<br />

120<br />

100<br />

80<br />

60<br />

40<br />

20<br />

0<br />

R 2 = 0.67 n=5<br />

0 5 10 15 20 25 30 35<br />

Age (years)<br />

R 2 = 0.91 n=5<br />

300 400 500 600 700<br />

Basic density (kg m-3)<br />

NSW<br />

Mature<br />

Predicted from Density<br />

Linear (NSW)<br />

NSW<br />

Mature<br />

Predicted from Age<br />

Linear (NSW)<br />

Figure 5. Modulus <strong>of</strong> rupture (MOR) <strong>of</strong> E. <strong>dunnii</strong> as a function <strong>of</strong> basic density <strong>and</strong> <strong>of</strong> age. NSW <strong>plantation</strong><br />

material are shown as solid square <strong>and</strong> the regression equation was calculated using these data. Mature native<br />

forest tree are shown as large solid circle, <strong>and</strong> an age <strong>of</strong> 34 years was selected for ease <strong>of</strong> graphic display.<br />

Predicted MORs for 3 <strong>plantation</strong>s aged 12, 16 <strong>and</strong> 32 years using the relationship with density are shown as<br />

open circles, while MORs predicted from the relationship with <strong>plantation</strong> age are shown by open squares.<br />

Modulus <strong>of</strong> elasticity measures stiffness <strong>of</strong> <strong>wood</strong>. It is less <strong>of</strong> a problem with hard<strong>wood</strong>s than pine<br />

although juvenile <strong>wood</strong> from <strong>plantation</strong>s may potentially have unacceptable MOE. MOE increased<br />

with density in five NSW <strong>plantation</strong> E. <strong>dunnii</strong>, while the relationship with tree age was less accurate<br />

(Figure 6). The linear relationships <strong>of</strong> tree age or basic density with both MOE <strong>and</strong> MOR may not be<br />

the most appropriate relationship as logarithmic functions could also be used. In both cases the data<br />

show both MOR <strong>and</strong> MOE increase over time, <strong>and</strong> that neither tree age nor basic density is a wholly<br />

satisfactory explanatory variable (except in the case <strong>of</strong> the MOR basic density relationship). MOE is<br />

influenced by density <strong>and</strong> micr<strong>of</strong>ibril angle, with micr<strong>of</strong>ibril angle accounting for more variation than<br />

density (Evans <strong>and</strong> Ilic, 2000; Yang <strong>and</strong> Evans, 2003). In combination, density <strong>and</strong> micr<strong>of</strong>ibril angle<br />

can account for over 90% <strong>of</strong> MOE in <strong>plantation</strong> eucalypts (Evans <strong>and</strong> Ilic, 2000; Yang <strong>and</strong> Evans,<br />

2003). The relationship between MOE <strong>and</strong> density <strong>of</strong> mature native forest E. <strong>dunnii</strong> differs from the<br />

relationship developed using <strong>plantation</strong> E. <strong>dunnii</strong> (Figure 6). MOE <strong>of</strong> mature E. <strong>dunnii</strong> was higher<br />

than predicted using <strong>plantation</strong> E. <strong>dunnii</strong> despite similar basic density (Figure 6). As micr<strong>of</strong>ibril angle<br />

typically declines with tree age (eg. Lindstrőm et al. 1998), <strong>and</strong> as large gains in MOE are realized<br />

with relatively small changes in micr<strong>of</strong>ibril angle (eg Yang <strong>and</strong> Evans, 2003), it seems likely that


MOE <strong>of</strong> mature native forest material is likely to be more heavily influenced by lower micr<strong>of</strong>ibril<br />

angle than younger <strong>plantation</strong> material, despite similar basic densities.<br />

MOE can also be predicted from acoustic measurements such as FAKOPP. Of three acoustic<br />

instruments tested, Henson et al. (2004) found FAKOPP gave the most accurate predictions <strong>of</strong> MOE.<br />

Predicted MOE <strong>of</strong> older E. <strong>dunnii</strong> <strong>plantation</strong>s using a linear relationship between MOE <strong>and</strong> FAKOPP<br />

showed MOE to be greater than 14 GPa in st<strong>and</strong>s aged 12 years or older.<br />

MOE (GPa)<br />

MOE (GPa)<br />

25<br />

20<br />

15<br />

10<br />

25<br />

20<br />

15<br />

10<br />

5<br />

0<br />

5<br />

0<br />

R 2 = 0.36 n=5<br />

0 5 10 15 20 25 30 35<br />

Age (years)<br />

R 2 = 0.63 n=5<br />

300 400 500 600 700<br />

Basic density (kg m-3)<br />

NSW<br />

Mature<br />

Predicted from Density<br />

Predicted from FAKOPP<br />

Linear (NSW)<br />

NSW<br />

Mature<br />

Predicted from Age<br />

Predicted from FAKOPP<br />

Linear (NSW)<br />

Figure 6. Modulus <strong>of</strong> elasticity (MOE) as a function <strong>of</strong> basic density, <strong>and</strong> <strong>of</strong> age <strong>of</strong> E. <strong>dunnii</strong>. NSW<br />

<strong>plantation</strong> material are shown as solid square <strong>and</strong> the regression equation was calculated using these data.<br />

Mature native forest tree are shown as large solid circle, <strong>and</strong> an age <strong>of</strong> 34 years was selected for ease <strong>of</strong><br />

graphic display. Predicted MOEs for 3 <strong>plantation</strong>s aged 12, 16 <strong>and</strong> 32 years using the relationship with<br />

density are shown as open circles, while MOEs predicted from the relationship with <strong>plantation</strong> age are shown<br />

by open squares, <strong>and</strong> MOEs predicted from FAKOPP are shown as open triangles.<br />

Acoustic instruments have been successfully used to predict log <strong>quality</strong> for other purposes. Dickson et<br />

al. (2005) successfully used a DIRECTOR to segregate logs into three stiffness classes. Ply<strong>wood</strong><br />

MOE produced from veneers peeled from each <strong>of</strong> these three classes was positively related to acoustic<br />

velocity, once again showing the importance <strong>of</strong> MOE for structural timber <strong>and</strong> the use <strong>of</strong> acoustic<br />

measurements to predict end product <strong>quality</strong>.


Strength Group (SD)<br />

MOR <strong>and</strong> MOE have a major impact on <strong>wood</strong> utilisation. Under the Australian strength classification<br />

system using AS/NZS2878:2000 (St<strong>and</strong>ards Australia 2000), species are classified into ‘strength<br />

groups’ based on minimum mean MOR <strong>and</strong> MOE values. Individual sawn boards are then assigned Fgrades<br />

depending on the size <strong>and</strong> type <strong>of</strong> defects present. For seasoned timber, there are eight strength<br />

groups for SD1 to SD8 in descending order <strong>of</strong> strength. Figure 7 shows the strength group <strong>of</strong> E. <strong>dunnii</strong><br />

improving with age. The predictive equation indicates a tree age <strong>of</strong> 22 years before SD4 is attained,<br />

<strong>and</strong> 30 years for SD3. Material selected from a progeny trial at age 9 years for high density had a<br />

superior strength group (SD 3) than the overall relationship. It would be assumed that this material<br />

would maintain its overall stronger SD rating age, thus showing the value <strong>of</strong> Tree Improvement<br />

programs in developing <strong>plantation</strong> forestry.<br />

SD group<br />

8<br />

7<br />

6<br />

5<br />

4<br />

3<br />

2<br />

1<br />

0<br />

y = -0.1369x + 7.1108<br />

R 2 = 0.8407<br />

R 2 = 0.84 n=4<br />

0 5 10 15 20 25 30 35<br />

Age (years)<br />

NSW <strong>plantation</strong><br />

Selected high density NSW material<br />

Mature<br />

Linear (NSW <strong>plantation</strong>)<br />

Linear (NSW <strong>plantation</strong>)<br />

Figure 7. Strength (SD) group as a function <strong>of</strong> age for E. <strong>dunnii</strong> <strong>grown</strong> in NSW <strong>plantation</strong>s (solid square)<br />

with 9 year old material selected for high density shown as a solid diamond. Only the four data points <strong>of</strong> non<br />

selected material were used to develop the regression relationship. Mature native forest tree are shown as<br />

large solid circle, <strong>and</strong> an age <strong>of</strong> 34 years was selected for ease <strong>of</strong> graphic display.<br />

Conclusion<br />

Wood from <strong>Eucalyptus</strong> <strong>dunnii</strong> <strong>plantation</strong>s show increasing basic density as st<strong>and</strong>s age. Basic density<br />

was correlated, although perhaps not causally related to many other <strong>wood</strong> <strong>quality</strong> traits. These traits,<br />

including shrinkage <strong>and</strong> structural characteristics such as hardness, MOE <strong>and</strong> MOR, showed linear<br />

increases with both basic density <strong>and</strong> st<strong>and</strong> age. The increasing MOR <strong>and</strong> MOE corresponded to<br />

increased strength <strong>and</strong> reduced strength grade (SD grade), highlighting its higher <strong>quality</strong>. As these<br />

traits, along with growth characteristics such as tree volume <strong>and</strong> diameter, heavily influence end<br />

product recovery <strong>and</strong> value, then it should be realised that <strong>plantation</strong> material which is usually<br />

harvested at younger ages than native forest material may be <strong>of</strong> different <strong>quality</strong>.


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