1. Introduction
Over the last two decades, tropical land use change, especially deforestation and forest degradation, has accounted for 12% to 20% of global anthropogenic greenhouse gas (GHG) emissions [
1]. Accurate assessment of forest carbon stocks is crucial for the successful implementation of climate change mitigation policies [
2]. Currently quantifying forest carbon stocks accurately remains a global challenge [
3].
The forest area of Mexico is approximately 65 million hectares, which represents one third of the national territory, 51% corresponds to temperate forests and 49% to tropical forests [
4]. The forests of
Abies religiosa Kunth Schltdl. et Cham. are important sinks of atmospheric carbon, it is an endemic conifer of Mexico [
5] that is distributed mainly between 2400 and 3600 m altitude along the Transmexican Volcanic Belt. The main ecological function of the
A. religiosa forest is as a preferred host for monarch butterfly populations that come to hibernate in Mexico [
6], in addition to providing environmental services and serving as a reservoir of biodiversity of organisms such as saprotrophs and ectomycorrhizae [
5]. Economically, it is important to highlight the use of wood as raw material for pulp and paper production and ecotourism for its impressive scenic beauty [
7].
Studies on subterranean ecosystem processes are relatively scarce compared to those dealing with aboveground plant traits, since roots and rhizosphere are hidden in the soil [
8]. Root studies are usually based on time-consuming and therefore costly methodologies [
9]. Their limited information is due to the difficulty in obtaining complete root systems and because of the large amount of work involved in individual measurement, sometimes requiring heavy machines in their extraction [
10,
11,
12], the same can be said of the reduced conceptual framework and existing terminology [
13]. Consequently, it should be noted that the methodologies proposed so far show how complicated it is to avoid root losses and a certain percentage are broken during excavation [
11]. Therefore, estimates of root biomass in trees are scarce, which leads to a lack of concise data on the global carbon stock found in a given environment [
12].
In tree-dominated ecosystems, the aboveground biomass (BA) of vegetation is usually derived from soil survey data. Biometric measurements of trees are converted into biomass values using an empirical allometric model [
14]. An allometric model is a tool that allows relating one or more easily measured variables (for example diameter at breast height, height, age) to estimate a variable that is difficult to measure (for example volume, biomass, carbon) [
15].
The use of allometry tools allows estimating the biomass of a particular species with greater accuracy [
13,
15] are obtained from the extraction of trees and measurement of a data set for calibration [
16,
17]. The sample size for allometric equations for root biomass is small compared to those for aboveground biomass, due to the difficulties of excavating whole root systems [
17], but which is necessary in all ecosystems to generate an allometric equation per species, allowing accurate biomass estimation by taking only a few data in a more accessible way and avoiding destructive sampling [
16].
Several current publications are oriented to estimate the carbon stored in the different aerial components (trees, understory and necromass) in different types of vegetation [
3,
18,
19], unfortunately the root component of carbon storage lacks estimates, Rojas-García and collaborators [
20] conducted a database of allometric equations performed in Mexican forests, which resulted that of the 478 equations found in the literature only 5 belonged to tree roots, this limits the knowledge of the total amount of carbon stored in different ecosystems and the generation of climate change mitigation strategies. The objective of this study was to develop an allometric equation to estimate the belowground biomass of
A. religiosa.
3. Results
The data obtained in the field from the 61 trees of A. religiosa extracted with the root system were subjected to multiple regression analysis to obtain the variables that best fit to generate the allometric model, the variables were: diameter at the base (DB), where the data obtained ranged from 0. 08 to 6.28 cm and total height (TH), which ranged from 0.06 to 3.56 m. The height variable was the main index when selecting the trees to be extracted, since starting with the first tree, we looked for specimens that were increasing in height, avoiding sampling individuals of the same height. Regarding the root biomass of A. religiosa, it varied according to the following factors: trees of small total height presented greater root biomass than trees of medium height, this is related to the fact that their ecological conditions of development differ, such as soil humidity, availability of space, competition for solar radiation, among others, the results obtained are in the range of 0.03 to 0.525 kg of root biomass per tree.
The equation generated in this study for the estimation of root biomass in A. religiosa trees can be used in other forests of the same species that meet certain conditions, such as the same type of soil, climate with similar ranges of temperature, precipitation and altitude above sea level, mainly. This model can be used in all stages of development of A. religiosa trees without increasing the range of error.
If the intention is to estimate the amount of root biomass present in an oyamel forest that complies with the ecological conditions, the allometric model can be applied by simply measuring the variables of total height and diameter at the base of the tree, which optimizes costs, time and labor in comparison with the total extraction of the individual. Rojas García et al. [
20] mention that, to estimate the aerial biomass, the main variables considered to generate an allometric model are the total height and normal diameter of the tree, which results in that the same independent variables are mainly used to estimate the aerial and root biomass, which allows a better estimation of the possible variation due to ecological conditions.
The minimum model with the best fit and significantly less error was the one based on diameter, so this model was chosen. The equation proposed for
A. religiosa is:
where:
RFW=Root fresh weight (g)
D=Diameter (cm)
Model testing generated significant regression with fit 80.9% of cases (F(1,998)=5058, p < 0.0001, r2 = 0.8352).
Confidence intervals indicate that models based on height+age, diameter+age, height+diameter and the full model did not differ from each other (
Table 1), while models with single variables height, diameter and age differed.
Of all the variables evaluated, the number of root branches and diameter of the main root were not used in the development of the allometric model. According to the attributes evaluated, the model was able to retain an extrapolation rate of the biomass contained in the trees of A. religiosa.
The clustering analysis showed four groups related to all the variables and an isolated tree (
Figure 3). With these groups, a discriminant classification analysis was performed to determine the most important variables in the model indicated by * in
Table 2. In all cases the Mahalanobis distances obtained were significantly different, associated with a single discriminant factor explaining more than 99.003% of the variance between groups and with an eigenvalue greater than 16. Subsequent assignment analyses allow us to assign 100% of the individuals with their corresponding category, so that in future work it will be possible to distinguish the biomass according to the height and diameter of the individuals.
The groups formed correspond, for the most part, with the stages of crop development (sapland, coppice, latizar and forest) [
28]. In addition, it is possible to subdivide the fustal considering trees larger than 35 meters as possible seedlings, and in this case, with greater biomass. The grouping characteristics standing height, number of root branches, tree fresh weight, root fresh weight, tree dry weight and root dry weight (
Table 2) had not been previously considered in the suggested categories, so the estimation models were less accurate, so the current proposal was much more accurate and allows extrapolation to other areas with similar forest cover in terms of species composition.
By applying the equation obtained, the database was generated in .xlsx format, which requires entering the diameter at the base and total height of the tree of interest to obtain the root biomass, this allometric model can be applied in forests of A. religiosa with similar conditions to soil type, rainfall, height above sea level, average temperature, to name a few.
Quantifying the biomass present in all the components of an ecosystem makes it possible to estimate the availability of resources, the carbon storage capacity and, in turn, the loss of carbon and the factors that cause it over time, in order to develop strategies for its conservation [
29]. Among these strategies is the payment for ecosystem services, specifically carbon credits, which consist of developed countries buying Reduced Emission Certificates from developing countries in order to reduce the over-accumulation of greenhouse gases. In most of the projects that are within this carbon market only receive payment for the vegetation present in the aerial component (trees and shrubs) because as mentioned in this study it is complex to estimate the biomass of the soil component, however, it is necessary to quantify it in its entirety in order to generate greater benefits to the owners of the forests and it is here when the generation of allometric models is highly applicable and important.