1. Introduction
The leaf water content (LWC) is an important physiological parameter in the discipline of plant science [
1]. The water content of leaves and their transpiration rates control the extent of stomata opening [
2], thus influencing the rate of photosynthesis [
3]. In turn, this limits the growth rates and biomass productivity of the plant [
4]. Furthermore, LWC also plays a role in determining salinity tolerance [
5] and even affects oviposition preferences of herbivorous insects [
6,
7].
Consequently, measuring LWC may provide information on various physiological aspects of plants such as their current levels of water stress [
8,
9,
10], drought tolerance [
11,
12], salinity tolerance [
5], flammability [
13,
14], and photosynthetic rates [
15]. Survey studies have indicated that genetics (particularly classification at a family or order level) have the largest impact on LWC, while precipitation and climate have smaller effects [
16]. Nevertheless, there is significant spatial variation in LWC between different habitat types. Researchers have also highlighted that LWC will be an important variable to measure in future studies of large-scale trait variations [
16].
The most common method of measuring LWC is by oven-drying the leaves to a constant mass and determining the loss of mass. However, this method is destructive and can be time consuming, particularly when large numbers of leaves must be analysed. Consequently, in order to better understand the distribution of LWC within plants and ecosystems, rapid methods of measuring this parameter are required. This is particularly significant for the eucalypts (tribe Eucalypteae; principally comprising the
Eucalyptus,
Corymbia, and
Angophora genera), as these species are a crucial part of many Australian ecosystems [
17].
Rapid, non-invasive analytical techniques have been reported for measuring LWC [
1,
10,
18], principally using near-infrared spectroscopy (NIRS) [
19,
20]. This analytical technique uses light with a longer wavelength than visible light to investigate the presence of key functional groups (e.g., OH, CH, NH) in a sample matrix. The benefits of NIRS include its speed (no sample preparation), low cost (no ongoing expenses), portability, and broad applicability to a range of sample types [
8,
21]. Recent technological advances in reducing the size and cost of NIR instruments have made them highly suited to use in field surveys investigating various analytes [
20,
22,
23,
24].
However, there are limited studies applying NIRS for the prediction of LWC in eucalypt species. This tribe of plants is somewhat unique in possessing a thick waxy cuticle layer on their leaves [
25], which acts to reduce water loss [
26]. This physiological feature may potentially complicate the development of NIRS models for the prediction of LWC. Yang, et al. [
27] used NIRS to predict the leaf water potential (Ψ
leaf) in
E. camaldulensis, but not the absolute LWC. Similarly, Datt [
28] was able to predict the equivalent water thickness in several eucalypt species using NIRS, but not the gravimetric water content (i.e., the absolute LWC). In contrast, Kumar [
29] was able to predict LWC in six
Eucalyptus species by using a laboratory NIR instrument. This appears to be the only study to date reporting NIRS calibration for LWC that can be utilised across different eucalypt species. Furthermore, there are no comparable studies incorporating the
Corymbia genus. Consequently, the aim of this study was to apply portable NIRS instrumentation for the rapid prediction of gravimetric LWC in eucalypt leaves from several species across two genera (
Eucalyptus and
Corymbia).
As a secondary aim, NIRS was also trialled for the prediction of leaf thickness in these species. Although this parameter is not usually measured with NIRS, it was thought that the leaf thickness could be indirectly predicted from the magnitude of absorbance produced from all of the compounds (e.g., structural carbohydrates, proteins, and water) present in the leaves. Leaves with a smaller thickness would consequently be expected to show less absorbance overall, and vice versa for thicker leaves. This is supported by previous work demonstrating that leaf thickness was the best predictor of NIR reflectance and internal light scattering [
30]. Therefore, NIRS might be able to rapidly screen for leaf thickness at the same time as measuring leaf water content.
2. Materials and Methods
2.1. Eucalyptus Leaf Samples
This study was conducted in May 2022 on a grazing property in Central Queensland, comprising an open woodland of mixed eucalypt species. Leaves of varying maturity stages were collected from six different
Eucalyptus and
Corymbia species (
E. populnea,
C. citriodora,
E. platyphylla,
E. tereticornis,
E. melanophloia, and
C. tessellaris). Between 2 and 4 trees were sampled for each species; 20 leaves were collected for each species (only 19 for
E. tereticornis). Effort was made to collect leaves from multiple canopy levels in each species. The leaves sampled were from the ‘intermediate’ and ‘adult’ maturity stages [
31].
The NIR spectra were collected from the fresh leaf samples as soon as practicable after collection (approx. 10–20 min).
2.2. Collection of NIR Spectra
Spectra between 908–1676 nm were collected directly from the eucalypt leaves using a MicroNIR OnSite handheld spectrometer (Viavi, Santa Rosa, CA, USA). This instrument has a diffuse reflectance geometry. The instrument was calibrated using dark and light reference measurements every 10 min. The following parameters were used: 6 nm resolution; 100 ms integration time; 1 scan per spectra. Spectra were collected in triplicate, from different locations on each leaf. No tile was placed behind the leaves during measurement, to simulate the situation that would take place during in-field measurements. The adaxial and abaxial sides of each leaf were both randomly sampled, again to simulate a simplified method for potential in-field use. Previous work indicated some variation in the spectral absorbance from the adaxial and abaxial sides, albeit relatively minor [
32].
In addition to collecting spectra from all of the fresh leaves, NIR spectra were also collected from 20 E. populnea leaves half-way through the drying process, and another 5 E. populnea leaves when they were completely oven-dried (0% moisture). Furthermore, spectra were collected from 30 E. populnea leaves that had naturally dried (to varying extents) after falling off the trees. Inclusion of these samples provided a wider range of moisture contents for the creation of a robust prediction model.
In total, 174 leaf samples were scanned, each in triplicate (n = 522 spectra). One leaf sample (n = 3 spectra) was excluded due to outlier values. The spectra were not averaged prior to data analysis.
2.3. Measurement of LWC and Leaf Thickness
The leaf water content was measured by oven drying the leaves at 65 °C until they reached a constant mass. The loss in mass was recorded for each leaf and the moisture content was calculated and expressed as a percent of the fresh weight as per the following formula:
Leaf thickness (recorded to ±0.1 µm) was measured near the centre of each leaf, using an engineer’s micrometer (RS PRO External Micrometer; item code 705–1213; range 0–25 mm; accuracy ±0.004 mm). Care was taken to ensure that the thickness was not measured through the central vein, which could have influenced the results.
2.4. Model Development
The NIR spectra were exported in ASCII (*.csv) format and subsequently imported into Unscrambler X software (version 10; Camo Analytics; Oslo, Norway) for chemometric analysis.
The spectra were split into 2 sets: the calibration set (comprising all 5 eucalypt species, but excluding all E. platyphylla spectra), and the independent test set (comprising all of the E. platyphylla spectra). Each model was built and cross-validated using the entire calibration set, then applied to the independent test set to assess its performance. Full cross-validation was performed on each calibration model using the leave-one-out (LOO) approach. All models were limited to a maximum of 7 factors to avoid the potential of over-fitting.
Partial least squares regression (PLS-R) was performed in Unscrambler X, using leave-one-out (LOO) cross-validation. Various spectral pre-processing treatments were trialled, including standard normal variate (SNV) normalisation, multiplicative scatter correction (MSC), and first and second derivative treatments using differing numbers of smoothing points for the Savitzky–Golay algorithm. Abbreviations for these pre-processing methods indicate the derivative and number of Savitzky–Golay smoothing points used. For example, 1d5 indicates 1st derivative with 5 smoothing points. Each pre-processing method was trialled on the entire calibration set.
Support vector regression (SVR) was also trialled as an alternative algorithm method to PLS-R. An Epsilon SVR model was used, with a radial basis function, gamma value of 0.008, and 2 classes.
Graphs were drawn in R Studio, running R version 4.0.5 [
33].
2.5. In-Field Application
Finally, the NIR method was applied in-field to measure the LWC and leaf thickness of every leaf found on a small E. populnea sapling (~2.5 m height; 67 leaves) in central Queensland. The process of NIR spectra collection was quite rapid, with up to 7 leaves scanned per minute.
In addition to collecting the NIR spectra, the height of each leaf above the ground was measured using a laser distance measurer (Ozito LMR-025), to determine whether there were any correlations between leaf height and LWC/thickness.