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& Diels):
detection methods for heart rot and false heartwood
Maaike De Ridder1,2, Jan Van den Bulcke1, Hans Beeckman2 and Joris Van Acker1
Abstract
Both resistance and velocity measurements were performed on planted and natural limba trees in the Democratic
Republic of Congo. While 2 velocity measurements per tree are sufficient for the quick diagnosis of rotten or
hollow trees, a compilation of 16 resistance profiles is necessary to distinguish the so-called false heartwood
(limba noir). On those two-dimensional reconstructions, small peaks in resistance correspond roughly with the
boundaries of limba noir. Detection methods are influenced by diameter, wood density and the presence of
buttresses. Further research on density profiles is recommended to analyse these influences and the link with
both detection methods.
1. INTRODUCTION
Limba (Terminalia superba Engl. & Diels) has a very large distribution: from Sierra Leone until the
north of the DRC from the east and from the south, until northwestern Angola [1]. This heliophilous
species - often with large buttresses - is typically found in secondary forests and fallows [7] but also in
plantations in Bas Congo (Democratic Republic of Congo). The presence of heart rot in older trees and
the formation of a so-called limba noir or false heartwood [2] alters the popularity of this species.
The incidence of these two wood anomalies makes limba a very suitable species for the study of
detection methods for as well heart rot as wood discolorations. This study is set up within the
framework of sustainable forest management of tropical forests: detection of anomalies before
exploitation prevents useless cutting and the loss of trees with an ecological function as e.g. seed trees.
This implies certain conditions for detection methods: in situ applicable, not too expensive, fairly
quick and easy to interpret. Two methods that meet all conditions are resistance [5, 6] and acoustic
detection methods [9], mostly used as control methods for more specialised detection techniques. This
case study wants to answer the following questions: (a) Are resistance and acoustic methods able to
detect rot and/or wood discolorations like limba noir? (b) Which factors influence the measurements
(density, buttresses, diameter)?
3. RESULTS
3.1. Diagnosis of wood rot
Variation in resistance and velocity within and between sample trees is moderate to large. For
instance, the differences in velocity within a tree are considered not significant (ANOVA, p = 0.72).
However, it is important to keep the original values since averaging would only permit to detect rot in
the central part of the tree. According to the boxplot, normal velocity values are situated between 1000
and 1650 m s-1. When rejecting the velocity outliers, the mean velocity of mature limba trees is 1288 ±
120 m s-1 (n = 174). This can be considered as the reference velocity (V ref). The relative decrease in
velocity can be calculated like this:
Relative decrease of sound velocity = (Vref – Vmes) / Vref * 100 (1)
On a total of 184 velocity measurements, only 7 measurements or less than 4 % appear unusually low,
ranging from 298 to 917 m s-1. The corresponding relative decrease of sound velocity ranges from 29
to 77 %. The lowest record of velocity (298 m s-1) is excluded for further analysis because the sensor
was placed in the rotten area, a position that causes diverging values. Compared to the table on the
distributor’s website (www.fakopp.org), this decrease should equal a decayed area of 75 % and more
(hollow trees). On the other hand, 3 measurements are extremely high, reaching velocities of 1676 to
2181 m s-1. Mostly, those maxima are associated with the presence of buttresses. Before converting the
resistance profiles, we compared the outliers of the velocity values with the resistance profiles.
Sometimes, the decrease in velocity corresponds with a sudden decrease in resistance that is clearly
visible (tree 8) while in other cases, this decrease can also appear to be subtle or even absent (tree 27)
(Figure 2). Looking at the notes on the outer state of the tree and the wood cores, we can see that rot
detection methods generally confirm what is suspected. Only little rotten zones near the bark, with
velocities from 1050 to almost 1200 m s-1, are still classified as healthy because they are not
considered as outliers.
After transformation, a significant Pearson correlation of 0.23 (p < 0.01) was found between velocity
and minimum resistance. Still, this correlation is not high enough to use the minimum resistance as a
criterion for rot detection. Correlations do not improve when only outliers are included for analysis.
(a)
(b)
Figure 2 – Resistance profiles of two infected trees:
(a) Tree 8: both resistance profiles visualize a large rotten zone and have low velocities (ca. 850 m s-1).
(b) Tree 27: measurement B has a low velocity (917 m s-1), but the decrease in resistance could be ascribed to
natural density variations if velocity measurements were absent.
4. DISCUSSION
Normally, mature limba trees are sensitive to heart rot. In this case, less than 5 % of the sampled trees
was infected, possibly the consequence of good planting material and favourable site conditions.
Rotten or hollow trees are mostly found next to little paths that are regularly used by the local
population. Using our detection methods, hollow and heavily rotten trees are detectable, where before
only detected hollow trees using velocity measurements [9]. With only two measurements per tree, the
resistance profiles are sometimes hard to interpret. Velocity measurements give a more straightforward
value that can be immediately compared to normal velocity values. Therefore, velocity measurements
are recommended for quick diagnosis. The range of allowable velocity measurements is still large (650
m s-1) so we propose further research on the diagnosis of small cavities or wood rot within the lower
end of this range (1050-1200 m s-1).
We confirm earlier results on the influence of density [3]. Higher diameters generate higher velocities
in several tropical tree species, while previous research concluded the opposite [3]. We could expect
that even-aged trees with a larger diameter are fast-growing so less dense and with a smaller velocity.
Still, the trends in several African tree species are far more significant than in the previous study. The
reason for this phenomenon is unknown and could be linked to wood anatomical features.
Transforming resistance profiles into point values is not recommended. Resistance profiles are most
appropriate for mapping of the impact, shape and location of wood anomalies. When analyzing the
reconstructions, small resistance values often indicate rotten areas while peak values can be associated
with the boundaries of limba noir. Acoustic measurements do not provide clear-cut reconstructions
because they were made on stem disks, ignoring the influence of sound propagation in an axial way.
Since stem disks often show cracks, these anomalies are also detected by velocity measurements,
complicating reconstructions. Acoustic reconstructions should be based on standing trees above the
buttresses.
Resistance and velocity values are not easy to link since they weren’t taken at exactly the same spot
but 5 to 10 cm one below the other. The presence of buttresses also influences results but there is no
trend visible in velocity or resistance measurements. Buttresses sound quite hollow but can cause
reaction wood once they join the main stem, creating additional density variations. Analysis of density
(buttresses, wood cores and stem disks) is recommended to find the missing link between resistance
and velocity measurements.
(a) (b)
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