1. Introduction
In recent years, fertilization has been highlighted as a potential method to improve tree growth in boreal forests, increasing biomass production and providing more raw material for the bio-economy [
1]. Despite this, limited attention has been paid to the self-regenerated broadleaf tree species which occur naturally in these stands, such as silver birch (
Betula pendula Roth.) and downy birch (
Betula pubescens Ehrh.), which are common in Sweden. The majority of these birches are commonly removed during pre-commercial thinning operations and left to decay, even though their diameters are large enough for further industrial processing to produce, for example, furniture or engineered wood products (EWP) [
2]. Short-term forest growth is almost instantly increased through fertilization, which can be applied to both mature [
3,
4] and young forests [
5]. Numerous studies in North American temperate broadleaved forests have found a positive growth response to fertilization [
6], yet research about the growth response in boreal broadleaf forests is limited.
Conifers are evergreen, while broadleaved species are usually deciduous; they drop their leaves at the end of each growing season. This difference in plant phenology means deciduous birches must build up their canopies annually, while the native conifers retain needles between growing seasons and likely have a longer response time to fertilizer [
7,
8]. The response in wood formation should also differ since nutrient addition that drastically increases conifer growth can result in decreased density [
9]. A diffuse-porous broadleaved species like birch can be expected to have a different growth response, both in increment and wood formation.
Adding nitrogen and mineral nutrients to enhance growth, i.e., fertilization, has been successfully demonstrated for various tree and forest types [
10]. Studies of intensive forest management in Sweden have found that fertilizers can potentially increase the volume production by 26%–200% [
1,
11,
12]. Previously published information about the response of birch to fertilization is inconsistent. Paavilainen [
13] remarked that birch usually has a positive response to fertilization, but it was smaller than the response of conifers. Hoyle and Bjorkbom [
14] also reported an increase in birch growth after fertilization. Viro [
15] studied a fertilized mixed stand with pine, silver birch, and downy birch. Viro found that fertilization did not affect the total biomass, but instead, more biomass was allocated to branches and less to foliage in the fertilized stand than the unfertilized stand. Moilanen [
16] reported a weak response to fertilizer treatment for silver birch growing on peat-lands relative to the stem growth and height growth for their control stand. Furthermore, Kaunisto [
17] found that on mined peatlands, fertilization with nitrogen, phosphorus, and potassium, slightly increased the growth of birch seedlings.
The effects of increased growth rate on the structure of birch wood anatomy have seldom been studied [
18]. For most wood species, an increased growth rate may change wood properties [
19] as the growth rings become wider. The wood that is first formed in the tree, the juvenile wood, often has wide growth rings [
20] associated with different, and less desirable, mechanical properties than mature wood (or ‘outer-wood’) [
21]. Rapid growth in young trees can increase the total proportion of juvenile wood in the final product as the growth rings become wider [
21]. As trees become older, the growth rate and ring width generally decreases [
22].
Wood density, strongly correlated to wood mechanical properties, depends on the cellular ultrastructure, the amount of cell wall material, lumen cavities, vessel size and their frequency [
23,
24], as well as extractives and the wood’s moisture content. Wood density is, therefore, a commonly used wood quality indicator, related to wood properties, such as shrinkage and mechanical strength, as well as to pulp properties and yield [
25]. The cell structure is mainly influenced by cambium age and ring width [
26], and the within tree radial variations can be useful for distinguishing between age and growth effects [
27]. In some conifers, wood density is directly affected by the tree growth rate, as shown for
Pinus cooperi [
28] and for Norway spruce (
Picea abies Karst), where density is negatively correlated with ring width [
29,
30]. Generally, a wood fiber’s function is to support the tree, thus their ultrastructure is of great importance to define the mechanical properties of wood [
24]. In some coniferous species, cell diameter can affect cell wall thickness, as found by Cuny et al. [
31]. In their study, the amount of material deposited was almost constant, with the rate of cell expansion driving cell wall deposition and determining density.
Some research suggests that density is hardly affected by the growth rate in diffuse-porous trees [
19,
25,
32], due to the uniform growth ring pattern. Beech, a diffuse-porous species with similar wood to birch, may experience a slight reduction in density as ring width increases [
33], although Peters et al. [
34] found a contradictory relationship, due to a reduction in the ratio of fibers to vessels. There is no consensus on how the growth rate affects the wood density in birch. Ollinmaa [
35], according to Loustarinen and Verkasalo [
36], reported no difference in density between slow and fast-growing silver birches. Velling [
37] reported a weak correlation between growth rate and density in mature silver birch, while Bhat [
38] found a significant negative relationship for similar material. A negative correlation was also found for juvenile silver birch by Liepiòð and Rieksts-Riekstiòð [
39]. The studies mentioned here had no assessment of properties at the cellular level.
While there is evidence that a more mature cambium in silver birch produces denser wood [
38,
39,
40,
41,
42], knowledge about the effect of increased growth on wood anatomy and subsequent wood density is scarce for silver birch. A better understanding of density variation as a function of radial growth is important for silver birch, as it is an important species for European industries [
43,
44]. Learning more about wood variation could facilitate the increased use of silver birch in products, such as furniture, flooring, and interior decorations. The objective of this study was to compare the growth-related changes in anatomical wood properties of young silver birch with and without fertilization, and to characterize the annual radial variation of wood anatomy. For this purpose, there were three main hypotheses;
Fertilization of young silver birch will:
- (1)
increase growth ring width;
- (2)
decrease cell wall thickness;
- (3)
decrease wood density.
2. Materials and Methods
The material used for this study was from a site located at the Toftaholm estate, in south-west Sweden (57°0′ N, 14°3′ E). The climate is humid continental, and the mean annual temperature is 6.3 °C, with 766 mm mean annual precipitation [
45]. The site is predominately mesic sandy moraine, and there are smaller wetter areas with a thin peat layer. Acid granite dominates the bedrock with a few additions of ultrabasic rock. The terrain is leveled with only minor variation in elevation. The site class index, according to Hägglund and Lundmark [
46], is G32, corresponding to a mean annual increment of 11.3 m
3 ha
−1 potential yield of Norway spruce. The site was wind-felled by a storm in 2005 and then clear-cut. The site had soil scarification and was reforested with planted Norway spruce and natural birch regeneration. Pre-commercial thinning occurred once in 2017.
The fertilization experiment consists of two adjacent stands; one stand was fertilized (treated) by helicopter in April 2014 and April 2016. The amount of nitrogen (N) supplied on each occasion was 150 kg ha
−1 of nitrogen, which was determined from leaf N-concentration. The supply of other macro and micronutrients was adjusted to initial target ratios of each element to N [
47]. If the ratio of a nutrient element to N was below its target value, an extra amount was added on the next occasion. Threshold leaf concentrations and proportions of the essential nutrient elements for attaining unlimited growth were determined in the earlier laboratory [
48] and field experiments [
49]. These proportions correspond with recommendations given by Brække [
50]. The mean C/N ratio in the top-soil (0–10 cm) prior to fertilization was 24.3 ± 0.6 and 24.5 ± 0.6 (±SE) at the fertilized and unfertilized stand, respectively.
The trees were sampled at the end of May 2018. In the fertilized and the unfertilized stand, ten silver birch (
Betula pendula Roth.) trees were sampled, making a total of 20 trees.
Table 1 presents some characteristics of the target trees. The trees were subjectively selected based on diameter at breast height (DBH, 1.3 m height from ground height). No damaged trees were accepted. The trees were 4–10 years old (at DBH), and all of the wood was therefore considered to be juvenile [
51,
52].
Two discs were removed from each tree at breast height (1.3 m), as samples from 1.3 m high generally provide a good estimate of the whole tree density value [
53]. The wood samples were initially stored in a freezer (−20 °C) in plastic bags until further sample preparation occurred. From each stem disc, two cuboids were prepared with a knife and hammer. The cuboids measured 10 mm tangential, the full pith-to-bark radial length, and 15 mm longitudinal. Each sample was prepared from the south direction of the disc. The cuboids were cut from wood that was free from knots, cracks, or areas of reaction wood.
The first cuboid from each stem was measured using the water-displacement method as described by Siau [
54] to determine basic density; calculated as the oven-dry matter (kg) divided by the green volume (m
3) of the specimen. The second cuboid from each stem was used to determine the age, growth of each target tree, double cell wall thickness, and number of vessels per square millimeter. Micro-sections were prepared using a sledge microtome (WSL lab-microtome, Switzerland). Thin sections (≈20 µm) were cut, stained with 1% safranin solution, washed and dried in a stepwise alcohol procedure, and finally mounted in Canada balsam, following the procedures as described in von Arx et al. [
55]. Disposable and high quality NT cutter blades were used to ensure clean and quality sections [
56,
57]. The semi-automated uplift function of the sledge microtome was used to ensure the constant thickness of the samples during the cutting procedure. The light microscope Olympus BX63 and the software program Olympus cellSens, were used for making measurements of ring width and for taking images on the mounted sections.
Measurements were performed along the radial axis, from the pith towards the bark. Mean ring width for the four years before treatment, 2010–2013, was measured to calculate the relative growth rate after treatment. Three of the fertilized trees were excluded in the analysis of growth before and after treatment since they were less than two years old when the treatment started. Basal area (BA) increase was calculated as an approximation of overall tree growth, and bark thickness was not included [
22]. In addition, the increase in BA for a given year (BA
year) was estimated using tree ring widths (RW). The total BA for a given year (tBA
year) was calculated by summing any previous years’ RW values to estimate radius for the end of a year (RAD
year). This radius then had the relevant year’s RW subtracted (RAD
year−1). All radius values were converted to BA values using the formula for a circle’s area (π × RAD
2). The BA growth for a given year (BA
year) was equal to tBA
year minus tBA
year−1 for 2015 to 2017.
All sampled trees had complete growth rings (excluding the pith) for 2015, 2016, and 2017, so growth rings were photographed for these years. The open-source freeware ImageJ 1.52j was used to measure wood anatomical properties, as this software has been successfully used in previous studies [
58,
59]. On each growth ring image, five 0.025 mm
2 squares were assessed in the middle of each ring width. Latewood was excluded from the analysis as defined by Luostarinen and Möttönen [
60]; the 3–4 layers of flattened cells at the end of each growth ring. The number of vessels and double cell wall thickness, hereafter called cell wall thickness, was measured in the radial direction in each square. The average number of vessels in the five sections was transformed so that vessels per mm
2, was the result for one growth ring. Cell wall thickness was measured in micrometers for 30 walls per square, in total 150 measurements per growth ring.
The statistical software packages SPSS 25.0 statistical software (SPSS, Chicago, IL, USA) and R (R Core Team, 2019) were used for the following analyses of data. In SPSS, a linear regression model (Equation (1)) was used to analyze the results of the relationship between density and cell wall thickness and density and ring width.
where
(2015–2017) is the dependent variable,
is the regression coefficient,
is the independent variable (average cell wall thickness, or average ring width, 2015–2017),
is the intercept, and
is any unexplained variance (the model error term).
Linear mixed models were built in R using the lme4 package (Bates, Maechler, and Bolker, 2012) and the ‘lmer’ function. This allowed for the use of binary variables, and the inclusion of fixed and random effects, to better suit the data set. The models were produced to predict average cell wall thickness per ring (CWt) and per tree average density (Dens) as a function of measured variables and treatment. The general model form (Equation (2)) was:
where
is the response vector (either Dens or CWt),
is a parameter matrix for the fixed effects (to be estimated),
is a design matrix which includes the measured traits or factors for each individual,
is a design matrix of random effects,
is a vector of unobservable random variables (random effects), and
is a vector of the residual variance not explained by the model. Random effects were used to show relatedness between values. The first random effect was for tree ID as observations were nested by tree. The second random effect in the model included an interaction term for age and year. Ring age and year were retained since they relate to stem age and growing season conditions.
The goodness of fit was assessed using output from R’s summary() function, type 3 ANOVA, and plotting the residual values against the fitted values. The predictor variables (RW, vessel number, BA
year, DBH, and treatment) were initially all added to a model. The summary output for each model in R provided model coefficients and
p-values for each variable. The specified linear mixed models were fit by reduced maximum likelihood (REML), so output
t-tests used Satterthwaite’s method. Variables were removed from the model as a more economical model is desirable, and to avoid errors associated with overfitting. The variable with the highest
p-value was iteratively dropped (backwards selection) and the process repeated until all remaining factors had significant
p-values (α = 0.05) in the model (Mod 1). This backward stepwise selection was then paired with forward stepwise selection [
61] to build a model from the variables with the two highest
p-values (Mod 2) and another with the highest
p-value variable (Mod 3) for comparison. Model residuals were plotted as histograms and against predicted values. The anova() function was used to compare Mod 1 to Mod 2, Mod 2 to Mod 3, and Mod 1 to Mod 3, as it provided Akaike information criterion (AIC), Bayesian information criterion (BIC), and log likelihood (LL) values. For ANOVA tests comparing model fits, the models were refit using maximum likelihood (ML) instead of the REML. A model is generally considered the best if AIC, BIC, and LL values are low, and residuals are normally distributed, compared to other models.
4. Discussion
More knowledge about juvenile wood mechanical properties is needed to better utilize material from early thinning [
2,
44]. Forest management activities can have both positive and negative consequences, which managers need to consider; for instance, the association between faster growth rates and reduced density [
33]. Related to this is the juvenile response to fertilizer application, which is quite well understood for coniferous species’ [
1,
11,
12]. However, little consideration is given to the fertilizer response of naturally regenerated birch, often growing in coniferous stands. Here, the results indicate how Swedish silver birch wood anatomy and density may be influenced by fertilizer, to assist managers who are considering fertilizing their mixed stands, or users of birch wood.
The results of this study suggest that fertilizing a mixed stand of silver birch can increase annual ring width. This is in line with hypothesis 1, as well as previous findings from greenhouse experiments [
16,
62]. Although the fertilized trees increased their basal area growth, it was only by 5% compared to the unfertilized trees (
Table 3). This could be explained by the soil conditions, which were considered fertile. Therefore, it is possible that nutrients were not largely limiting growth, and that the fertilization had a less extreme effect than if applied to a nutrient-limited site [
63]. This is in line with Paavilainen [
13], who also encountered a weak response to fertilization of birch on a fertile site.
From the microscope analysis, it was apparent that fertilized stems had thinner cell walls, in line with hypothesis 2, and more and smaller vessels than the unfertilized stems. This supports the theory that higher nutrient availability can support more foliage, which requires a larger number of vessels to supply water to the crown, although not studied here. The differences in wood formed during the 2017 growing season between treatments are not due to differences in climate as the two sites were adjacent. The random effects in the mixed model included a term for a year, which interacted with age (Age:Year), so this model parameter would include any climate influence. Year and age accounted for a very small proportion of model variance, despite 2016 being a drier year for southern Sweden [
45] and 2016 relative growth being lower than for 2014. It is likely that climate (Year) indirectly affected the modeled response variables by influencing other explanatory variables, like vessel number and ring width, or had limited influence when the effect of treatment was included in the model.
If another factor determined wood anatomy more than fertilizer status, then the unfertilized stems should have had more diameter growth in the pre-treatment years (before 2014) and would have been a similar size to the fertilized stems of the same age. The faster growth rate is associated with both younger stem vitality and as a response to fertilization. Vessel diameters were not fully studied here, yet from visual inspection, rings with more vessels tended to also have smaller vessels. This needs to be investigated further.
Regarding the variation in cell wall thickness, it was poorly explained by ring width. The initial linear model showed no correlation in the fertilized stand, but cell wall thickness was to some degree correlated to ring width for the trees from the unfertilized group. As this study was not a highly controlled laboratory experiment, it is hard to draw any direct conclusions. Density was slightly influenced by ring width, although the best fitting mixed model only included treatment. There could be a potential trade-off in the nutrient-limited stems so that an increase in ring width requires a reduction in cell wall thickness [
31], which was not present in the fertilized stems.
The lowest number of vessels were found in the oldest cambial age growth rings in the unfertilized trees, and had an average value of 95 (std. dev: 28). Bhat [
38] had a much lower number of vessels per mm
2 of 75.2 (std. dev: 42.8) in mature silver birch, which could be explained by the difference in cambium age [
64]. As the tree is growing and the distance from the pith increases, a reduction in the number of vessels, and an increase in the size of vessels, also occurs in other
Betula spp. [
64]. The number of vessels decreased with increasing age, so that 2017 values were lower than 2015 for both the fertilized and the unfertilized trees in this study. Although the vessels decrease in number, they increased in size, similar to the results of Fukazawa [
27] in Asian
Betula spp. This could be explained by the theory in Hacke et al. [
65], that the fiber matrix is approximately proportional to that of the conduit system, hence the thickness of the cell wall must increase when the vessels increase in size to avoid implosion. A tree that grows more rapidly, such as the fertilized trees in this study, needs more voids according to theories of changes to the mechanical constraints in the growing tree [
66,
67]. Here, the best fitting model for cell wall thickness had a negative coefficient for vessel number, meaning that as the number of vessels increased, the cell wall thickness decreased.
For many species, ring width and density are negatively correlated [
23], yet here this was not observed. In the simple linear fit, ring width also had lower correlations with both density and cell wall thickness for the fertilized stands, compared to the unfertilized stands. One explanation could be that the additional nutrients enabled the trees to increase growth without jeopardizing strength properties [
68]. A negative correlation between ring width and wood density was also found for unfertilized juvenile silver birch in a study by Liepiòð and Rieksts-Riekstiòð [
39], and in this study, the mixed models coefficient for ring width was also negative. However, since the models for average wood density as a function of ring width did not significantly improve model fit, it is likely that there are other factors that determine density. Fukazawa [
27] also found growth rate had no effect on the wood density of diffuse-porous Japanese birches.
It is important to consider the effects of cambial age on stem wood density [
52], as the relative fiber wall thickness increases in birch as the tree gets older [
27,
38]. The trees’ average density seemed to increase with increasing cambium age in
Figure 2, yet including the random effect of age did not improve the predictive power of ring width or basal area in the mixed models. This indicates that once age is accounted for, growth could be increased without decreasing wood density, if conditions are improved with the addition of fertilizer. Hypothesis 3 was confirmed as a fertilizer treatment that had a negative coefficient with wood density, yet a controlled experimental site would help to remove the age effects.
The fertilized trees had a wider range of values (higher standard deviations) for most of the measured properties. This is likely due to the wider age range for the fertilized trees, 4–8 years, compared to 8–10 for the unfertilized trees. Another issue is that by selecting trees of a certain diameter class, the wider growth rings in the fertilized stems guaranteed the trees would be younger than the unfertilized trees. It is hard to remove the influence this sampling strategy had on age class distribution if the effect of fertilizer on ring width is a true effect. Naturally regenerated birch is common in Swedish forestry, but this method of establishment results in a diverse range of seedling conditions. More controlled conditions could help endorse these findings and further support the use of fertilizer to increase the growth rate of birch.
In line with other studies [
69], the individual tree explained more of the model variance than age or year. Here, cell wall thickness was highly correlated with density and would result in a singular model fit if used as a predictor of density. The excluded variables, ring width, and BA
year, were not significant determinants of average cell wall thickness or stem average density, based on ANOVA output and model fit. In all models, the variable with the largest estimated coefficient was treatment. In line with this study’s hypotheses, these results indicate that a fertilizer treatment will slightly reduce the wood density and cell wall thickness, but increase the growth rate, of juvenile silver birch.