The diverse array of end-products, which jack pine yields upon harvest [
25], suggest that in-forest forecasting of end-product potential could lead to important operational advancements in terms of informing product-based inventories, enabling the identification and prioritization of stands for harvest according to real-time market-driven requirements or existing capabilities of conversion centres, improving value recovery, and enhancing overall segregation and merchandizing efficiency. Historically, a range of approaches for estimating end-product potential of standing trees and harvested logs have been advanced [
5]. Non-invasive methods based on the deployment of external tree and log morphological-based indices to infer end-product potential have generated mixed results [
44,
45,
46]. For example, external characteristics such as stem size (diameter, height, and taper) and crown dimensional variables (diameter and length) have been shown to be significantly related to a number of key internal wood characteristics, which underlie end-product type and quality. However, the explanatory power of the derived prediction models has been weak. Multiple regression models developed for a suite of Silviscan-derived attributes (
me,
wd,
ma,
dr,
dt, and
co) for 495 white spruce (
Picea glauca (Moench) Voss) trees, which deployed tree size and crown dimensional predictor variables, were only able to explain no more than 13% of the variation for any of the key attributes (
me,
ma, and
wd, [
45]). Somewhat better results were reported by Kuprevicius [
46] who found that similarly structured regression-based models for a sample of 43 white spruce trees could explain 50% of the variation in the static modulus of elasticity.
Invasive methods including the deployment of destructive methods such as the extraction of increment cores followed by their Silviscan processing, yield explicit attribute estimates that can be used directly to infer end-product potential without consequential error or bias [
29]. Although such invasive methods are widely used in silvicultural-based research investigations [
47], the logistical challenges, and the time and fiscal commitments required to implement this approach, have largely negated its operational deployment in pre-harvest assessments of end-product potential [
5]. By contrast, non-invasive acoustic-based approaches in which commercially-relevant attributes can be estimated on-site, in real-time, and at sufficiently lower cost than invasive methods, represent a viable alternative for forecasting end-product potential [
24]. However, the limited scope of the traditional acoustic-based inferential framework, species-specific nature of acoustic-based attribute relationships, and the general lack of associated performance measures in terms of the degree of bias and predictive precision, warranted a further in-depth prerequisite examination of these issues. Hence, the consequential importance of the results presented in this study in terms of solidifying and advancing the potential utility of the acoustic approach in boreal forest management., albeit for a single species (jack pine).
4.1. Fibre Attribute-Specific Acoustic Velocity Relationships for Standing Jack Pine Trees and Sampling Considerations
The results for the jack pine trees assessed in this study indicated that the proportion of variation explained by the linear regression specification varied by attribute. The highest level of explanatory power was found to be associated with the primary relationship
in which 71% of the variation in the dynamic modulus of elasticity was explained, as quantified by the coefficient of determination (
r2 = 0.71,
Table 4). This result exceeds that of Chen [
48] for standing Norway spruce (
Picea abies (L.) Karst.) trees who reported a
r2-equivalent value of 0.28 based on a simple linear regression model specification. Likewise, these results for jack pine exceed those reported by Newton [
14] for standing red pine trees (i.e.,
r2 value of 0.40). Other studies, which evaluated the relationship between acoustic velocity of standing trees and the static modulus of elasticity of clear xylem samples or resultant end-products (e.g., sawn boards) employing a regression model specification that omitted the wood density term
, have produced largely mixed results. For example, Amateis and Burkhart [
49] found no statistically significant (
p ≤ 0.05) relationship for standing loblolly pine (
Pinus taeda L.) trees. However, for standing Norway spruce trees, Fischer [
50] found a weak but significant (
p ≤ 0.05) relationship (
r2 = 0.13). Moderate levels of explanatory power (mean
r2 = 0.44) and significant (
p ≤ 0.05) relationships were reported for standing Sitka spruce (
Picea sitchensis (Bong.) Carr.) and western hemlock (
Tsuga heterophylla (Raf.) Sarg.) trees by Wang [
51]. Nanami [
52] also found a significant (
p ≤ 0.05) relationship with a moderately high level of explanatory power (
r2 = 0.59) for standing Sugi (
Cryptomeria japonica D. Don.) trees.
Apart from the results provided for red pine trees by Newton [
14], published results for the secondary attribute—acoustic velocity relationships examined in this study have been largely limited to examining acoustic-based relationships pertaining to the prediction of microfibril angle and wood density [
9,
53]. Based on an assessment of the same suite of acoustic-based relationships investigated in this study but for red pine, similar but not identical results were obtained. Specifically, deploying Silviscan-based attributes and time-of-flight acoustic velocity measures from 54 red pine trees, statistically significant (
p ≤ 0.05) regression relationships were obtained for
me,
wd,
wt,
co, and
sa. Along with the two additional attribute relationships that could be established for jack pine but not for red pine (
ma and
dr), the portion of variability explained was greater for the jack pine relationships than that for the corresponding red pine relationships. Specifically, 40% of the variation was explained in the dynamic modulus of elasticity for red pine versus 71% for jack pine, 14% of variation was explained in wood density for red pine versus 30% for jack pine, 45% of the variation was explained in cell wall thickness for red pine versus 66% for jack pine, 27% of the variation was explained in fibre coarseness for red pine versus 42% for jack pine, and 43% of the variation was explained in specific surface area for red pine versus 61% for jack pine. However, in terms of predictive precision, the relationships for red pine were slightly more precise than those observed in jack pine. This was attributed to the greater inherent variability in the attribute values for the jack pine trees relative to the those for red pine trees. For example, attribute-specific coefficients of variation for the 61 jack pine sample trees (
Table 1, this study) were approximately twice that of red pine (see
Table 3 in Newton [
14]). Red pine is a more genetically invariant species relative to jack pine, which may partially explain the difference in the magnitude of attribute variation between the two species (sensu [
25]).
Study variation among the attribute—acoustic velocity relationships is also not unexpected given differences among investigations in terms of sampling procedures, analytical approaches, instrumentation, species, and locale. Furthermore, internal tree factors such as variation among sample trees in knot distributions, embedded voids, growth rates, temperature and moisture conditions of the xylem when measured, and external factors such as tree size, local competition around the sampled tree, and site conditions, are also potential sources of error that could contribute to the degree of unexplained variation and reduced the statistical significance of the attribute—acoustic velocity relationships [
54,
55,
56]. Thus yielding the approach used in this study, which attempted to minimize some of these known sources of variation: i.e., (1) usage of Silviscan-based attributes measured from xylem tissue sequences extracted via destructive stem analysis from standing-trees upon felling, (2) employment of a single calibrated acoustic sampling device for all sample trees, (3) systematic measurement of acoustic velocities at multiple circumferential positions, (4) selecting sampling trees from stands growing on similar site productivities, at equivalent stages of maturity, and with similar silvicultural histories, and (5) collecting acoustic velocity measurements during identical seasonal periods (early autumn). Nevertheless, the resultant regression relationships for jack pine could achieve only an overall moderate level of explanatory power.
One of the prime determinates underlying the potential deployment of in-forest acoustic-based attribute forecasting is the degree of precision required by the end-user. Differentiating individual standing trees by end-product potential, according to narrow design-based thresholds, requires a high degree of predictive accuracy. Quantitatively, the residual mean square errors along with the prediction and tolerance error intervals, provide insight into the predictive performance of the relationships when potentially deployed. Although the lack of attribute-specific design threshold values that can be explicitly linked to end-product potential hinders the ability to provide conclusive guidance on interpreting the acoustic-generated attributes, an examination of existing grading manuals for some of the potential end-product categories for softwood species can be informative (sensu [
14]). For example, threshold values for the modulus of elasticity associated with a specific lumber grade have been defined for machine stress-rated dimensional lumber products. The mean difference in the static modulus of elasticity value across 14 machine stress-rated lumber grades is approximately 0.7 GPa [
16]. The mean standard error of the estimate for the relationship between the dynamic modulus of elasticity and density-weighted acoustic velocity for jack pine is approximately 1.0 GPa. Furthermore, the corresponding error intervals suggest the 95% of future predictions for newly sample jack pine trees would have a range of ±2.4 GPa when using a Silviscan-equivalent wood density estimate (
Table 5) and ±2.7 GPa when using an acoustic-derived wood density estimate (
Table 7). These precision metrics suggest that the acoustic-based
me estimate would not be accurate enough to differentiate among these narrow grade classes, even if it is assumed that the
me within a standing tree is equivalent to that in its derived dimensional lumber product. However, combining the grade categories into a smaller set of discrete product grade classes may assist in overcoming this issue, depending on the within-class ranges used. For example, based on the NLGA [
14] machine stress-rated lumber specifications for spruce, pine, and fir boards, Paradis [
57] delineated three
me-based grade classes to represent lumber end-product potentials for black spruce. These three classes, denoted low, medium, and high grade, were differentiated by approximately 1.5
me units (GPa). Thus, if similarly applied to the jack pine, the dynamic
me estimate would still, however, not be precise enough to segregate an individual tree into one of these three classes (i.e., given the ±2.7 GPa expected error associated with each
me prediction). Consequently, increasing the class threshold widths, which would reduce the number of groupings, may be required with respect to segregating individual standing jack pine trees in specific grade classes.
Alternatively, stand-level sampling in which acoustic velocity and associated wood density estimates are obtained from a group of trees may be precise enough to yield a mean
me estimate accurate enough to differentiate stands, according to their end-product potential. For example, the mean
me estimate derived from acoustic velocity measurements from 30 trees within a stand along with acoustic-based density estimates, would be within ±0.5 GPa of the true mean value (
Table 7). Thus, in this case, the level of accuracy attained at the stand-level would be precise enough to segregate stands into one of the three grade classes based on the within-class
me range proposed by Paradis [
57]. Potentially, scaling acoustic-based stand-level mean attribute estimates to the forest level by integrating remotely-sensed forest inventory information could also be of utility when attempting to generate landscape-level wood quality property maps [
57,
58].
The expansion of the primary
me-
vd relationship resulted in the derivation of additional secondary acoustic—attribute relationships that may be of utility in the non-destructive estimation of end-product potentials of standing trees. Newton [
14] employed a similar experimental and analytical approach as what was used in this study to assess attribute—acoustic velocity relationships for standing red pine trees. Results of that analysis revealed significant (
p ≤ 0.05) regressions for five of the eight attributes studied (
me,
wd,
wt,
co, and
sa) with slightly lower performance metrics in terms of explanatory power and predictive ability. Although references to other studies employing a similar analytical framework are not readily apparent within the literature, the empirical findings presented for red pine and jack pine provide confirmatory evidence in support of the proposed acoustic-based inferential framework. For these additional attributes, such as wood density, microfibril angle, tracheid wall thickness, radial tracheid diameter, fibre coarseness, and specific surface area, similar issues arise as that discussed above regarding the interpretation of the modulus of elasticity estimates. Although the lack of direct linkages between within-tree attributes estimates and those within finished end-products limits the ability to identify and classify standing jack pine trees into discrete end-product categories, using the suite of attribute estimates could, nevertheless, provide sufficient guidance to stratify individual trees or stands into general end-product categories. Trees or stands with high stiffness and density values could be associated with having a greater potential to produce higher grade solid-wood end-products relative to those with corresponding lower values (sensu [
4]). Similarly, trees or stands with larger tracheid wall thickness and fibre coarseness values, could be inferred as having a greater potential to produce higher quality pulp and paper end-products than trees or stands with corresponding smaller values (sensu [
4]).
In terms of field sampling, recent results examining the effect of xylem temperature and moisture on acoustic velocity within standing semi-mature jack pine trees during the vegetative growing season, indicated that, although xylem moisture had no appreciable influence, acoustic velocity did declined in a linear fashion with increasing temperature [
59]. However, the temperature effect was not of consequential significance except when xylem temperatures approached their seasonal extremities (minimums (<5 °C) and maximums (>30 °C)). Consequently, this source of variation could be considered as random error provided that temperatures did not exceed these thresholds when acoustic sampling. Otherwise, the correction equation for standardizing acoustic velocities to a reference xylem temperature (20 °C), as provided in Newton [
59], could be utilized.
4.2. Non-Destructive Wood Density Estimation and Consequences on Its Use in Fibre Attribute Predictions
Irrespective of the magnitude of the portion of variability explained and with the exception of the relationship for the tangential tracheid diameter, the results of this study demonstrated that the in-forest acoustic approach could provide unbiased estimates of the dynamic modulus of elasticity, wood density, microfibril angle, tracheid wall thickness, radial tracheid diameters, fibre coarseness, and specific surface area, within standing jack pine trees. In accord with the parameterized primary and derived secondary acoustic-based relationships, estimates of wood density would be required for their operational deployment. The results of this study provide two potential non-destructive methods that could be used. Specifically, utilizing the wood density estimate derived from (1) an acoustic velocity measurement obtained using a time-of-flight tool (Director ST300) in combination with the
wd =
parameterized regression equation (Equation (5b),
Table 4), or (2) a drill resistance mean amplitude measurement obtained from the Resistograph profile in combination with the parameterized
wd =
regression equation (Equation (6),
Table 6). With respect to the latter method, previous studies have reported varying degrees of association between the mean amplitude values derived from micro-drilling resistance tools, such as the Resistograph, and wood density within standing trees. For example, Isik and Li [
60] reported a phenotypic-based correlation of 0.75 for eight-year-old loblolly pine (
Pinus taeda L.) clones. This would translate into an approximate coefficient of determination value of 0.56 based on a simple linear regression relationship, which is not dissimilar to that reported in this study (
r2 = 0.51,
Table 6). Employing a similar but not identical analytical approach but for red pine trees, Newton [
14] reported a statistically significant (
p ≤ 0.05) mean amplitude-wood density relationship for red pine trees. However, the portion of variability explained was lower than what was determined for jack pine (27% for red pine versus 51% for jack pine). Downes [
61] reported viable relationships for five eucaplypt plantations (
Eucalyptus globulus Lambill. (
n = 4), and
Eucalyptus nitens (Deane & Maiden) Maiden (
n = 1)) located in Northwest Tasmania (
n = 2) and Western (
n = 2) and South-Eastern Australia (
n = 1). Deploying a simple linear model similar in specificity to that employed in this study for the five separate plantations, Downes [
61] reported statistically significant (
p ≤ 0.05) mean amplitude-wood density relationships, which explained a moderate to high level of core-based density (e.g., coefficients of determination ranging from 0.66 to 0.87). Although intercept and slope values were generally stable and of similar magnitude across the sampling sites, slight differences were observed, particularly with regard to the slope term. Downes [
61] suggested that instrumentation-induced variation and sampling conditions were plausible determinates underlying these differences.
In consideration of the empirical evidence as provided in this jack pine study and those from past investigations [
57,
58], along with the results from analytical-based comparative assessments examining the performance of competing technologies (direct-based increment core extraction methods and indirect-based impact approaches, [
62]), it is evident that the drill resistance approach is a viable in-forest method for non-destructively estimating wood density. Logistically, however, when comparing the micro-drill resistance and acoustic-based approaches, the former approach would be more challenging to implement given the requirement for additional on-site equipment (Resistograph) and data management (i.e., on-site editing of profile output data streams in order to calculate a mean amplitude value for the xylem portion of the stem). For jack pine, the wood density estimate obtained via resistance drilling would only be marginally more precise than the acoustic-based estimate: approximately 1% to 2% increase in absolute width of the relative error intervals obtained via resistance drilling over that obtained through acoustic-sampling (cf.
Table 5 and
Table 6). Although recent advancements in automating the processing of Resistograph profiles in terms of generating mean amplitude values have reduced the computational burden (i.e., web-based computational software [
61]), the acoustic-based approach would be the most applicable for jack pine given that it requires the least amount of effort with regard to logistical requirements and data processing, provides a real-time on site density estimate, and is only marginally inferior in terms of predictive precision. Other low impact tools and techniques such as the mechanical-based Pilodyn impact device [
63] and near infra-red spectrometers [
64] could also be potentially used to estimate wood density non-destructively. However, assessing their utility and predictive performance was beyond the scope of this study.
The in-forest deployment of the acoustic-based prediction equations developed in this study will ultimately depend on the requirements of the end-user in terms of the accuracy of the point-estimate for a given attribute that is actually required. For example, if the relationships are used to stratify individual standing trees into various product categories (e.g., solid wood products versus pulp and paper) and then assign a potential grade class within the categories (e.g., select or economy grade for dimensional lumber products), then information pertaining to the accuracy of the point-estimate will be of the upmost importance. The provision of predictive performance metrics for each of the parameterized relationships enables end-users to assess the potential utility of the acoustic approach in their pre-harvest value-based inventory assessments (e.g., predictive intervals demarks the error range generated when using the equations on a newly sampled tree). For example, deploying an acoustic-based wood density estimate, the magnitude of the error arising from a
me,
ma,
wt,
dt,
co, and
sa prediction would be expected to be within approximately ±20%, ±39%, ±13%, ±8%, ±12%, and ±12% of their true values, respectively (
Table 7). The intervals for a
me and
ma are relatively large and, thus, would, in all likelihood, negate the ability to classify individual stand jack pine trees into narrow grade classes based on these two attributes. Alternatively, if the approach was used in the context of stand-level fibre attribute characterization in which acoustic sampling was conducted on a large number of individual trees within a given stand in order to generate a mean population-level estimate, then the stand-level prediction error intervals would be of the upmost importance. As shown in this study, the mean error arising from 30
me,
ma,
wt,
dt,
co, and
sa predictions would be expected to be within approximately ±4%, ±9%, ±3%, ±2%, ±3%, and ±3% of the true mean value, respectively (
Table 7).
4.3. Relationship between Tree and Log Acoustic Velocities and its Utility in Generating a Poisson Ratio Estimate for Jack Pine
Functionally, the relationship between acoustic velocity and the dynamic modulus of elasticity for standing trees is different from that specified for harvested logs. The latter relationship is expressed as
where
is the velocity of a mechanically-induced longitudinal stress wave (km/s). Logistically, the wave is created by hitting one of the log’s open cross-sectional faces with an impact tool. The wave propagates through the log until it reaches the opposite cross-sectional face and then returns. A resonance-based acoustic instrument, which is also placed on the open cross-sectional face at the time of impact, measures the velocity of the wave as it transverses the xylem tissue within the log (e.g., Hitman HM200, Fibre-gen Inc.). Conversely, for standing trees, it is the velocity of a mechanically-induced dilatational or quasi-dilatational stress wave that enters the circumference of the stem just above stump height (0.5 m) through an inserted impact probe which passes vertically through the xylem tissue transecting breast-height (1.3 m) and is circumferentially measured at a stem height of approximately 1.5 m via the upper-positioned receiving probe (e.g., Director ST300 as was used in this study;
Figure 1). Although the wave types differ along with their functional relationship with the modulus of elasticity, the velocity measurements have been shown to be empirically correlated.
More specifically, based on a simple linear regression model specification that was used to describe the relationship between
vl (dependent) and
vd (independent) for five coniferous species, Wang [
12] reported significant (
p ≤ 0.05) relationships with moderate to high levels of explanatory power (
r2 values of 0.93, 0.85, 0.71, 0.83, and 0.90 for Sitka spruce (
Picea sitchensis (Bong.) Carr.), western hemlock (
Tsuga heterophylla (Raf.) Sarg), jack pine, ponderosa pine (
Pinus ponderosa Dougl. ex Laws.), and radiata pine (
Pinus radiata D. Don), respectively). Deploying
vl and
vd measurements for the trees and accompanying 1st-order butt logs (≈ 0–20% height percentiles) for the trees used in this study, revealed a similar significant (
p ≤ 0.05) relationship with an approximately identical
r2 value (0.70) to that reported by Wang [
12] for jack pine (
r2 = 0.71). This degree of concordance of the velocity correlative relationships for standing trees and derived logs across multiple species, provides a measure of confirmatory support for the acoustic approach in terms of its overall consistency and agreement with expectation. Furthermore, Wang [
12] proposed that the ratio between
vd and
vl could be used to characterized species-specific differences between the wave types. Specifically, the mean
vd/
vl value across the five coniferous species assessed by Wang [
12] ranged from 1.07 to 1.36 with a mean value of 1.20. Analyzing the jack pine trees sampled in this study revealed that the ratio ranged from 1.04 to 1.31 with a mean value of 1.24. Again, the species-specific ratio that was reported by Wang [
12] for jack pine (1.21) was very similar to that obtained for the jack pine trees sampled in this study (1.24). More generally for conifers, calculating the mean ratio for all five species analyzed inclusive of the results of this study, suggest that the velocity of the dilatational wave measured in standing trees is approximately 1.22 times the velocity of the longitudinal wave measured in the derived logs.
The Poisson ratio (
P) is used as a covariate in the functional relationship between the dynamic modulus of elasticity and density-weighted acoustic velocity within standing trees (Equation (1)). It is also an important mechanical property of wood since it measures the relative deformation in the vertical plane (expansion) with respect to the deformation in the horizontal plane (compression). More specifically,
P is the transverse to axial strain ratio when a wood sample is axially loaded: the ratio of the deformation perpendicular to the direction of the load (transverse strain) relative to the degree of deformation parallel to the direction of the load (axial strain) [
65]. Given that the ratio varies within and between species and is difficult to estimate without laboratory testing and analyses, the ratio is commonly treated as an unknown constant when acoustic sampling. Empirically, however, Wang [
12] proposed an approach for generating species-specific Poisson ratio estimates deploying the ratio between tree-based
vd and log-based
vl measures. Mathematically, this involved three computational steps: (1) equating the
relationship developed for logs with the corresponding
relationship developed for standing trees, yielding the expression,
), (2) given (1), simplifying and rearranging this expression yields a relationship in which the velocity ratio can be expressed as a function of the Poisson ratio,
, and (3) given (2), deploying an empirical velocity ratio estimate for a given species yields a quadratic functional form, for which the positive root is taken as the Poisson ratio estimate. For example, employing the mean
vd value for the jack pine trees and mean
vl value obtained their extracted 1st-order butt logs, yields a velocity ratio value of 1.24 and the resultant quadratic function, 0.5376 − 0.5376
P − 3.0752
P2 Solving for
P gives a positive root value of 0.34, that is, the estimated Poisson ratio for jack pine.
This derived estimated Poisson ratio for jack pine is almost identical to the one estimate derived by Wang [
12] for their jack pine samples (
) and is not dissimilar to the one reported by Newton [
14] for the red pine (
). Furthermore, calculating the mean
P value from the values determined through mechanical testing on nine North American pine species (loblolly pine (
Pinus taeda L.), lodgepole pine (
Pinus contorta var. latifolia), longleaf pine (
Pinus palustris P. Mill.), pond pine (
Pinus serotina Michx.), ponderosa pine, red pine, slash pine (
Pinus elliottii Engelm.), and western white pine (
Pinus monticola Douglas ex D. Don)) as presented by Green [
65], yielded a value of 0.34 (minimum/maximum/standard deviation = 0.28/0.39/0.03). Thus, the acoustic-based estimate for jack pine is not discordant with that derived through stress testing for the group of other commercially-important pine species grown in North America. The value is also equal to the mean value of 0.34 that is commonly assumed for both hardwood and softwood species (sensu [
66]). An operationally plausible interpretation of the ratio is in terms of the plasticity of the xylem tissue of a given species to deform under pressure. For example, a ratio of 0.34 for jack pine, suggests that an upright piece of lumber would laterally expand approximately one-third as much as it would vertically compress when subjected to consequential axial loads. Based on a comparison of the acoustic-based Poisson estimates between species, suggest that red pine may exhibit a slightly greater rate of lateral deformity than jack pine when subjected to the same degree of axial compression (0.39 and 0.34 for red pine and jack pine, respectively). In addition to these generalized inferences, provision of a Poisson estimate provides a more complete description of the stiffness–acoustic velocity functional relationship, as represented by Equation (1).
4.4. Potential Utility of Acoustics in Value-Based Forest Management and Silvicultural Experimentation and Suggested Future Research Directions
Acoustic-based segregation of individual logs and trees based on wood quality characteristics and, by extension end-product potential within the upstream portion of the forest products supply chain, has been associated with increased operational efficiencies and associated profitability levels through the maximization of end-product value recovery [
23]. Additionally, the acoustic approach has been shown to be of utility for silvicultural-based experimentation where acoustic-based attribute estimates are used as wood quality response surrogates to various density management treatments. For example, in a study on quantifying the thinning intensity effect on wood quality (density-weighted dynamic wood stiffness) in Calabrian pine (
Pinus nigra Arnold subsp. calabrica) plantations in southern Italy, the acoustic approach was able to successfully differentiate treatment effects on end-product potential, which led to enhanced inference in terms of crop planning decision-making [
67,
68].
Recently, acoustic-based segregation analytics have undergone a period of rapid development for some intensely-managed and high-value pine species for which tree and log-based end-product estimation is considered fundamental to enhancing fiscal efficiency. Specifically, an acoustic-based generic segregation model developed for the tree–to–product portion of the forest products supply chain, has shown promise when parameterized for radiata pine in New Zealand [
69]. Notationally referred to as SEGMOD, this techno-economic segregation model utilizes acoustic-based internal fibre estimates of standing tree measured during pre-harvest inventories and (or) harvested logs at the time of extraction (in-forest, landings, mill gate), along with terrain information, external characteristics, fixed and variable cost inputs, and mill configuration assumptions, to generate tree-level fiscal worth expectations based on a given market type. Empirical results arising from an extensive set of model simulations applied to four operational case studies throughout New Zealand, indicated that standing-tree and in-forest landing-based segregation yielded significantly greater fiscal returns (≈10%) when compared to the results arising from the sorting yard, mill, and nil-based segregation scenarios.
Although similar analytical decision-support models have yet to be developed for boreal segregation operations, the results for jack pine provided in this study yields the prerequisite prediction equations for initiating such efforts. Furthermore, the scope of the acoustic-based attribute prediction relationships and overall inferential framework presented is much broader in terms of end-product-based fibre determinates. The results for standing jack pine trees empirically demonstrated that the acoustic approach could provide unbiased estimates of the dynamic modulus of elasticity, wood density, microfibril angle, tracheid wall thickness, radial tracheid diameters, fibre coarseness, and specific surface area. The jack pine relationships did, however, exhibit considerable variation in terms of the proportion of variation explained and predictive performance, which the error analyses revealed. Further research into plausible pathways that could reduce the amount of unexplained variation would be worthly of consideration. These efforts could include the identification and control of in-forest sources of systematic variation that negatively influences the attribute—acoustic velocity relationships [
56], and the potential employment of a standardization procedure to account for the effects of xylem moisture and temperature variation on acoustic velocity if found to be significant [
59,
70]. Provision of end-product-specific design-based threshold values for the attributes assessed in this study would also advance the acoustic approach in terms of in-forest segregation operations. For example, enabling the differentiation of trees or stands, according to their end-product potential based on a specific range of design-based values for one or more of the studied attributes. Attaining a more complete understanding of the wave propagation pattern within the xylem tissue in terms of its cross-sectional coverage for the primary and derived secondary relationships, would also be constructive in advancing the acoustic approach in fibre attribute prediction and associated end-product forecasting.