Revista Mexicana de Ciencias Forestales Vol. 15 (85)

Septiembre - Octubre (2024)

Logotipo, nombre de la empresa

Descripción generada automáticamente

DOI: https://doi.org/10.29298/rmcf.v15i85.1477

Research article

Relación de datos climáticos y de teledetección con la diversidad arbórea en un bosque templado

Relationship of climate and remote sensing data with tree diversity in a temperate forest

 

Jesús Emmanuel Méndez-Zúñiga1, José Manuel Zúñiga-Vásquez2, José Guadalupe Colín1*

 

Fecha de recepción/Reception date: 11 de abril de 2024.

Fecha de aceptación/Acceptance date: 8 de agosto de 2024.

_______________________________

1Tecnológico Nacional de México, Instituto Tecnológico de El Salto. México.

2Universidad Autónoma Chapingo, Unidad Regional Universitaria de Zonas Áridas. México.

 

*Autor por correspondencia; correo-e: jose_colin8@hotmail.com

*Corresponding author; e-mail: jose_colin8@hotmail.com

 

Abstract

Quantifying biodiversity is key to natural resource conservation; however, data collection can be time-consuming and costly. Given that climate and remote sensing data help in the prediction of species diversity, the objective of this study was to analyze the relationship of climate data and the Normalized Difference Vegetation Index (NDVI) with tree diversity in a temperate forest in Northern Mexico. Species richness (S), Simpson's (1-D) and Shannon's (H) diversity indices were calculated at 663 sampling sites. Subsequently, an exploratory regression analysis was performed to obtain regression models that would account for the relationship of tree diversity indices with the NDVI, climatic data, and the number of trees. The best model for each diversity index and its predictor variables was integrated into a Geographically Weighted Regression (GWR) model. The results showed that the relationship of diversity indices and predictor variables varies across the space. The variables showed greater predictive potential in the Northern and Northwestern part of the study area. The NDVI was the variable with the greatest relative influence in the explanation of the diversity indices; therefore, it can function as a proxy for factors associated with tree diversity.

Keywords: Spatial distribution, vegetation index, diversity indices, forest management, spatial regression, species richness. 

Resumen

Cuantificar la biodiversidad es clave para la conservación de los recursos naturales; sin embargo, la recolección de datos puede llevar mucho tiempo y resultar costosa. Dado que los datos climáticos y de teledetección ayudan a la predicción de la diversidad de especies, el objetivo de este estudio fue analizar la relación entre datos climáticos y el Índice de Vegetación de Diferencia Normalizada (IVDN) con la diversidad arbórea, en un bosque templado del Norte de México. Se calculó la riqueza de especies (S), los índices de diversidad de Simpson (1-D) y de Shannon (H) en 663 sitios de muestreo. Posteriormente se realizó un análisis de regresión exploratoria para obtener modelos de regresión que expliquen la relación de los índices de diversidad de árboles con el IVDN, los datos climáticos y el número de árboles. El mejor modelo de cada índice de diversidad y sus variables predictoras se integró en un modelo de Regresión Ponderada Geográficamente (RGP). Los resultados mostraron que la relación de los índices de diversidad y las variables predictoras varía a través del espacio. Las variables registraron mayor potencial de predicción en la zona Norte y Noroeste del área de estudio. El IVDN fue la variable de mayor influencia relativa en la explicación de los índices de diversidad, por lo que puede funcionar como sustituto de factores asociados con la diversidad arbórea.

Palabras Clave: Distribución espacial, índice de vegetación, índices de diversidad, manejo forestal, regresión espacial, riqueza de especies.

 

  

Introduction

 

 

Biodiversity loss is increasingly evident and worrisome, mainly due to the deforestation resulting from agricultural activities (Leija et al., 2021); consequently, interest in measuring and modeling it has increased (Gillespie et al., 2008).

The most popular strategy has been to model individual species distributions one at a time (Miller, 2010; Aceves-Rangel et al., 2018; Martínez-Sifuentes et al., 2021). However, spatial modeling of species diversity at the community level can generate significant benefits, particularly if many of these taxa are infrequently recorded (Ferrier and Guisán, 2006).

Remote sensing is one of the main tools available for the study and monitoring of biodiversity patterns across different spatial scales (Sánchez-Díaz, 2018), given that it is possible to assess the spectral characteristics of communities (Arekhi et al., 2017). Such monitoring and evaluation is based on establishing relationships between the spectral information in an image and the tree species diversity measured in the field (Madonsela et al., 2018). Likewise, vegetation indices estimated thanks to remote sensing allow us to know the different plant elements located on the surface of the Earth (Sancha, 2010; Vela-Pelaez et al., 2024).

Globally, several studies have used the Normalized Difference Vegetation Index (NDVI) to estimate tree diversity, based on its sensitivity to primary productivity, that defines the spatial variation in plant diversity (Madonsela et al., 2018). Given that such spatial variation or heterogeneity is an important driver of species richness, population structure, and complexity (Amatulli et al., 2018), it is of great interest to use techniques that may help understand such variation and, consequently, in due course, make better decisions.

The main objective of this study was to reveal the spatial relationship between tree diversity, NDVI, and certain environmental variables according to the Geographically Weighted Regression model. The hypothesis is that the relationship between tree diversity, the NDVI, and environmental variables vary across space.

 

 

Materials and Methods

 

 

Study area

 

 

The study area included the Adolfo Ruiz Cortines ejido, located in Pueblo Nuevo municipality, in the Southwestern region of the state of Durango, within the Western Sierra Madre (Figure 1). The climates present are temperate sub-humid C(w2) and semi-warm sub-humid (A)C(w2), with an average annual precipitation of 1 000 mm. The altitude above the sea level varies between 2 063 and 2 670 m (Rosales, 2016). The main vegetation types are mixed forests composed of the genera Pinus L. and Quercus L., the most representative vegetation types being pine forest (P), pine-oak forest (Pq) and oak-pine forest (Qp) (Rosales, 2016).

 

Vegetación = Vegetation; Bosque de pino = Pine forest; Bosque de pino-encino = Pine-oak forest; Pastizal inducido = Induced grassland; Vegetación secundaria arbustiva de bosque de encino = Shrub secondary vegetation of oak forest; Vegetación secundaria arbustiva de selva baja caducifolia = Shrub secondary vegetation of low deciduous rainforest; Vegetación secundaria arbórea de bosque de pino-encino = Tree secondary vegetation of pine-oak forest.

Figure 1. Location of the study area, main vegetation types, and distribution of sampling sites.

 

 

Dasometric data

 

 

Based on information from the ejido's Forest Management Program, the authors analyzed dasometric data of a total of 41 928 trees belonging to 20 species from 663 sampling sites circular in shape with a surface area of 1 000 m2 (Table 1).

 

Table 1. Analyzed species and number of trees.

Species

Number of trees

Pinus cooperi C. E.Blanco

561

Pinus durangensis Martínez

4 150

Pinus leiophylla Schiede ex Schltdl. & Cham.

7 532

Pinus teocote Schltdl. & Cham.

2 645

Pinus engelmannii Carrière

2 138

Pinus lumholtzii B. L. Rob. & Fernald

54

Pinus ayacahuite C. Ehrenb. ex Schltdl.

52

Pinus chihuahuana Engelm.

1

Juniperus deppeana Steud.

1 813

Cupressus spp.

1

Quercus sideroxyla Bonpl.

7 211

Quercus durifolia Seemen

1 253

Quercus laeta Liebm.

257

Quercus eduardii Trelease

195

Quercus crassifolia Bonpl.

21

Quercus splendens Née

132

Quercus rugosa Née

9 963

Alnus acuminata Kunth

3

Alnus spp.

10

Arbutus xalapensis Kunth

3 936

 

As indicators of alpha diversity, the total number of species (species richness S) and Simpson's Diversity Index (1) (Equation 1) (Simpson, 1949; Peet, 1974) were measured at each site, and, given that their value is inverse to the evenness (Equation 2) (Lande, 1996), diversity can be calculated as follows: 

 

    

 

Where:

 = Number of trees of a particular species

 = Number of trees of all the species

 = Proportional abundance of the species

 

Also utilized was the Shannon Index (Equation 3), which measures the average degree of uncertainty in predicting to which species a tree chosen at random from a collection will belong (Peet, 1974; Magurran, 1988). It acquires values between 0, when there is only one species, and the logarithm of S, when all the species are represented by the same number of trees (Magurran, 1988).

 

    

 

Where:

 = Shannon's Index

= Proportional abundance of the species

= Natural logarithm

 

 

NDVI and climate data

 

 

The NVDI was computed monthly and annually, using the Landsat 8 Surface Reflectance Tier 1 image set (30 m spatial resolution) in the Google Earth Engine® platform. These data have been atmospherically corrected using the LaSRC algorithm and include a cloud, shadow, water, and snow mask produced with CFMask and a per-pixel saturation mask. The images used correspond to the period from January 1, 2020 to December 31, 2020. One image was used for each month of the year with the least amount of clouds, and for the annual NDVI data, an average of the 12 images was calculated. Subsequently, the images were cropped to fit the study area.

In addition, data were obtained on mean annual precipitation and minimum, mean and maximum temperatures. These data were recorded in raster format (600 m spatial resolution) through the Digital Climate Atlas of Mexico and represent the average for the period 1902-2011 (Instituto de Ciencias de la Atmósfera y Cambio Climático, 2009).

 

 

Geoprocessing

 

 

Sampling sites were georeferenced and linked to the diversity index in a point-type shapefile. To match the diversity index data for each sampling site with the NDVI and climate information, a data extraction process was performed in ArcGIS 10.8® (ESRI, 2020), which consisted of extracting cell values from a raster based on a set of coordinate points. The resulting file was a point-type shapefile with attributes of coordinates, sampling site number, total number of trees per site, number of trees per species, diversity index values, monthly and annual average NDVI values, and climatic data of mean annual precipitation and minimum, mean and maximum temperatures.

 

 

Statistical analysis

 

 

An Exploratory Regression analysis was carried out using the ArcGIS 10.8® (ESRI, 2020) software to generate regression models that would explain the relationship between tree diversity and the NDVI and climate data. The dependent variables were the values of tree diversity indices, and the independent variables were the values of the NDVI, climate data, and the number of trees in each sampling site. In this analysis, all possible combinations of the candidate independent variables were evaluated. Unlike Stepwise Regression, which looks for models with high adjusted R2 values, Exploratory Regression tracks models that meet all the requirements and assumptions of the Ordinary Least Squares (OLS) method (ESRI, 2024).

 

 

    

 

Where:

 = Dependent variable

 = Intercept

 = Coordinates the ith observation

 = Number of independent variables

 = Slope

 = Independent variables

 = Model error

 

The Geographically Weighted Regression model was fitted in GWR 4.0.90 software (Nakaya, 2015), which also fits the Ordinary Least Squares (OLS) regression model and through an F-test compares the improvements of the GWR model about the OLS model (Nakaya, 2016).

 

 

Results

 

 

Exploratory Regression Analysis

 

 

An Exploratory Regression analysis indicated the combination of independent variables that best met the assumptions of the OLS method for each model. The independent variables for the regression model explaining species richness (S) were the NDVI values for the month of March (NDVIMarch), the number of trees present at each site, and the mean annual rainfall. For the Simpson (1-D) and Shannon (H) index models, the independent variables were the values of the January NDVI (NDVIJanuary) and the number of trees. All variables were statistically significant (p≤0.05).

 

 

OLS regression models

 

 

The regression equations adjusted for the diversity indices and their explanatory variables through OLS showed a low explanation of the observed variation (R2). The values of the variance inflation factor (VIF) of the explanatory variables of the diversity indexes did not show multicollinearity issues, as in all cases the values were lower than the reference value (7.5). In addition, the regression coefficients indicated that, in all cases, the NDVI was the variable of greatest relative importance, followed by the number of trees. In the case of species richness (S), the variable of least relative importance was precipitation (Table 2).

 

 

Table 2. Regression coefficients of OLS models adjusted for diversity indices.

Index

Variable

Regression coefficient (ß)

P value

Standard error

AIC

R2

Species richness (S)

Intercept

9.1347

0.000

2.09

2 239.05

0.15

NDVIMarch

2.0978

0.002

0.68

Number of trees

0.0178

0.000

0.002

Rainfall

-0.0055

0.033

0.002

Simpson (1-D)

Intercept

0.6621

0.000

0.02

-921.9

0.005

NDVIJanuary

0.1617

0.045

0.08

Number of trees

0.00005

0.007

0.0001

Shannon (H)

Intercept

1.3146

0.000

0.05

286.09

0.01

NDVIJanuary

0.4071

0.048

0.2

Number of trees

0.0009

0.033

0.0004

AIC = Akaike Information Criterion.

 

 

GWR models

 

 

The number of spatial units (sampling sites) considered for the fit of the GWR models was 663, the bandwidth was defined as 48 neighbors for the species richness (S) model and 46 for the Simpson and Shannon index models. The fitted GWR models showed lower AIC values than those obtained with the OLS models. These AIC values were 2 174.42 for the species richness (S) explanatory model, -1 000.37 for the Simpson's Index model, and 195.72 for the Shannon Index model. The above indicated that the GWR models had an improvement in error reduction, concerning the OLS models. In addition, based on the F-tests, the reduction in the sum of squares of GWR was determined to be significant (p<0.05) in all cases. This suggests that the GWR models are statistically different from the OLS models. Regarding the regression coefficients of the GWR model, it was also observed that the variable with the highest relative importance was the NDVI in all cases (Table 3).

 

Table 3. Summary statistics of the regression coefficients of the fitted GWR models for the diversity indices.

Index

Variable

Mean

Standard deviation

Minimum

Maximum

Average t-value

Species richness (S)

Intercept

6.8749

12.4785

-26.6498

33.518

1.4216

NVDIMarch

2.3361

2.1847

-1.9417

6.4714

1.4187

Number of trees

0.0183

0.0076

-0.0038

0.0307

3.8003

Rainfall

-0.0031

0.0136

-0.0344

0.0325

-0.5272

Simpson (1-D)

Intercept

0.5869

0.0683

0.4305

0.7446

12.1779

NDVIJanuary

0.6939

0.5533

-0.1278

2.3567

2.0044

Number of trees

-0.00005

0.0008

-0.0024

0.001

-0.1102

Shannon (H)

Intercept

1.1338

0.1859

0.6952

1.5882

9.6453

NDVIJanuary

1.7722

1.5229

-0.9463

5.8945

2.0255

Number of trees

0.0005

0.0019

-0.0049

0.0028

0.5003

 

The GWR approach allowed the mapping of model statistics and the analysis of their spatial variability. Figure 2A shows the spatial distribution of the NDVIMarch that corresponded to the one with the highest association with the species richness. The highest values of the regression coefficients of the number of trees tend to be distributed in the Northern part of the property (Figure 2B). Rainfall had a positive relationship with species richness in some spatial units, while in others it had a negative relationship (Figure 2C). The highest values for the regression coefficients of NDVIMarch were distributed in the Central-Northern part of the property, and the lowest, in the Northwestern portion (Figure 2D). Regarding the spatial variation of the coefficients of determination (local R2s), the highest values were registered in the Northern part of the property (Figure 2E). This variability in the local R2s indicates the locations where the variables explain the diversity indices to a greater or lesser extent.

 

A = Regression coefficient; B = Regression coefficients associated with a number of trees; C = Regression coefficients associated with rainfall; D = Regression coefficients associated with the NDVIMarch; E = Local R2s. Kilómetros = Kilometers.

Figure 2. Spatial distribution of GWR statistics for species richness.

 

Figure 3A shows the spatial distribution of the NDVI January, which exhibited the highest association with the Shannon index. The Regression coefficient of the number of trees had the lowest relative importance of the analyzed variables (Figure 3B). The highest values of relative importance for a number of trees showed a tendency to be distributed in the Northern part of the property. The Regression coefficient of the NDVIJanuary registered the highest relative importance, with the highest values distributed toward the Northwest of the property, while the lowest values were for the Northeast to Southwest area (Figure 3C). Finally, the local R2s had the highest values in the Northwest of the site, where the NDVIJanuary showed the highest relative importance. The lowest values were distributed in most of the analyzed samples (Figure 3D).

 

A = NDVIJanuary; B = Regression coefficient associated with a number of trees; C = Regression coefficients associated with NDVIJanuary; D = Local R2s. Kilómetros = Kilometers.

Figure 3. Spatial distribution of GWR statistics for Shannon index. 

 

The spatial distribution of NDVIJanuary showed the strongest association with Simpson's index (Figure 4A). The Regression coefficient of the number of trees registered the lowest relative importance of all the variables analyzed (Figure 4B); the highest values for the relative importance of number of trees were distributed in the Northern, Central, and Southern parts of the total distribution of the sites within the property. The lowest values were clustered to the Northwest of the property boundary and shared this distribution zone with the highest January values. The lowest values of the January regression coefficient were recorded from Northeast to East and South (Figure 4C). The local R2 values followed the same distribution pattern (Figure 4D).

 

A = NDVIJanuary; B = Regression coefficient associated with a number of trees; C = Regression coefficients associated with NDVIJanuary; D = Local R2s. Kilómetros = Kilometers.

Figure 4. Spatial distribution of GWR statistics for Simpson's index.

 

 

Discussion

 

 

Understanding how species diversity varies across space and exploring the processes and driving mechanisms involved have been fundamental goals of ecology (Balvanera and Aguirre, 2006) and have contributed to the development of different estimation methods that make it possible to improve the traditional classification methods (Hernández-Stefanoni et al., 2012).

In this study, the spatial variation of the relationship of tree diversity indices with NDVI values, climate data, and number of trees was analyzed using the GWR model. The use of spatially adjusted regression models, such as the GWR, improves the estimation of the statistics in comparison with OLS (Mallick et al., 2021; Cabral-Alemán et al., 2022; Lu et al., 2022); this was also observed in the present study. In addition, the use of GWR allowed the visualization of the predictive power of the independent variables analyzed, as well as the spatial distribution of the statistics and their respective mapping.

Notably, it was determined that the relationship of tree diversity indices with NDVI values, climatic data, and number of trees varied across space. Likewise, the explanatory power of each adjusted GWR model showed a tendency to vary in space; that is, there are areas where the R2 was higher: for example, in the Northern and Northwestern part of the study area. It should be noted that these areas coincide with the most productive areas of the property in terms of biomass and carbon (Cartus et al., 2014; Vargas-Larreta et al., 2017). In addition, in these areas, a higher relationship between the NDVI and tree diversity was observed; this can be explained by the direct relationship between the biomass and structural variables and the NDVI (Meng et al., 2016). Thus, the relaionship between IVDN and tree diversity supports the positive productivity-diversity assumption, which states that the relationship between productivity and species diversity follows an environmental gradient (Madonsela et al., 2017). Another important finding was the relationship of the diversity indices with the NDVI of different months; that is, species richness was more closely related to the NDVIMarch, while the Simpson's and Shannon's indices showed a closer relationship with the NDVIJanuary. These results are consistent with some precedents indicating that diversity indices tend to relate mostly to monthly NDVI values rather than to annual values (Meng et al., 2016; Madonsela et al., 2017); this has been directly related to the beginning of the growing season, as the onset of leaf senescence in trees marks an increase in NDVI values (Lu et al., 2022). For the study area, the growing season begins after cold conditions (January-March), characterized by low evaporation and greater soil moisture (Chávez-Gándara et al., 2017), agreeing with the period when the NDVI-diversity ratio was higher.

As for the relative influence of the explanatory variables of diversity, the NDVI was the most influential in explaining diversity indices; thus, it is an important predictor of tree diversity (Arekhi et al., 2017; Madonsela et al., 2018), and functions as a surrogate for factors associated with species diversity (Hernández-Stefanoni et al., 2023).

Another variable that helped explain the variability in the values of the diversity indices was the number of trees, which is the second variable in relative importance. This relationship is logical, given that diversity indices are a function of the relative distribution of individuals among species (Salami et al., 2021).

On the other hand, many other factors influence species diversity, mainly climate, topography, and soil properties (Song et al., 2021). However, the relative contribution of each variable may vary from one region to another (Song et al., 2021). Particularly, in the present study, no significant relationships were obtained between certain diversity indices and climate data. However, it was determined that rainfall may be a predictor of species richness in the study area, although this relationship has been more evident at larger scales (Xu et al., 2019).

Finally, as mentioned in similar studies, these types of results should be restricted to the working area, as they may be modified depending on the species examined, the environment, or the overall community members (Kiran and Mudaliar, 2012).

 

 

Conclusions

 

 

The relationship of diversity indices with NVDI, climate data, and a number of trees varies across space. The independent variables show greater predictive potential in the Northern and Northwestern parts of the study area; these results support the research hypothesis. NDVI has a high predictive power; therefore, it can function as a proxy for factors associated with tree diversity.

GWR is an effective method for analyzing the relationship between tree diversity and associated factors; in addition to being a technique that improves the results, it also contributes to the explanation of the spatial distribution of tree diversity.

Finally, these results serve as a basis for similar research in the region, and the use of statistical models that include the spatial component is recommended for a better understanding of diversity patterns and associated factors.

 

Acknowledgments

 

The first author is grateful to the National Council for Humanities, Science, and Technology (Consejo Nacional de Humanidades, Ciencia y Tecnología, Conahcyt) for the scholarship granted for his master's studies (CVU:1076190). We are grateful to Project No. r5x48w (11104) of the National Technological of Mexico/El Salto Technological Institute (Tecnológico Nacional de México/Instituto Tecnológico de El Salto), “Planificación de buenas prácticas para la conservación de la biodiversidad, a través de SIG en el ejido Adolfo Ruiz Cortines, Pueblo Nuevo, Durango” (“Planning of good practices for biodiversity conservation through GIS in the Adolfo Ruiz Cortines ejido, Pueblo Nuevo, Durango”).

 

Conflict of interest

 

The authors declare that they have no conflicts of interest.

 

Contribution by Author

 

Jesús Emmanuel Méndez-Zúñiga: planeación, levantamiento y análisis de datos, redacción del manuscrito; José Manuel Zúñiga-Vásquez: análisis de datos y revisión del manuscrito; José Guadalupe Colín: dirección, planeación, seguimiento del proyecto y revisión del manuscrito.

 

 

Referencias

Aceves-Rangel, L. D., J. Méndez-González, M. A. García-Aranda and J. A. Nájera-Luna. 2018. Potential distribution of 20 pine species in Mexico. Agrociencia 52:1043-1057. https://www.scielo.org.mx/pdf/agro/v52n7/2521-9766-agro-52-07-1043.pdf. (10 de agosto de 2024).

Amatulli, G., S. Domisch, M.-N. Tuanmu, B. Parmentier, … and W. Jetz. 2018. Data descriptor: A suite of global, cross-scale topographic variables for environmental and biodiversity modeling. Scientific data 5:1-15. Doi: 10.1038/sdata.2018.40.

Arekhi, M., O. Y. Yılmaz, H. Yılmaz and Y. F. Akyüz. 2017. Can tree species diversity be assessed with Landsat data in a temperate forest? Environmental Monitoring and Assessment 189:1-14. Doi: 10.1007/s10661-017-6295-6.

Balvanera, P. and E. Aguirre. 2006. Tree diversity, environmental heterogeneity, and productivity in a Mexican tropical dry forest. Biotropica 38(4):479-491. Doi: 10.1111/j.1744-7429.2006.00161.x.

Brunsdon, C., A. S. Fotheringham and M. E. Charlton. 1996. Geographically weighted regression: A method for exploring spatial nonstationarity. Geographical Analysis 28(4):281-298. Doi: 10.1111/j.1538-4632.1996.tb00936.x.

Cabral-Alemán, C., A. López-Santos, J. R. Padilla-Martínez and J. M. Zúñiga-Vásquez. 2022. Spatial variation of the relative importance of the soil loss drivers in a watershed of northern Mexico: a geographically weighted regression approach. Earth Science Informatics 15:833-843. Doi: 10.1007/s12145-022-00768-w.

Cartus, O., J. Kellndorfer, W. Walker, C. Franco, … and J. M. Michel F. 2014. A national, detailed map of forest aboveground carbon stocks in Mexico. Remote Sensing 6(6):5559-5588. Doi: 10.3390/rs6065559.

Chávez-Gándara, M. P., J. Cerano-Paredes, J. A. Nájera-Luna, V. Pereda-Breceda, … y S. Corral-Rivas. 2017. Reconstrucción de la precipitación invierno-primavera con base en anillos de crecimiento de árboles para la región de San Dimas, Durango, México. Bosque 38(2):387-399. Doi: 10.4067/S0717-92002017000200016.

Environmental Systems Research Institute (ESRI). 2020. ArcGIS Desktop: Release 10.8. Redlands, CA, United States of America. ESRI.

Environmental Systems Research Institute (ESRI). 2024. How Exploratory Regression Works. https://pro.arcgis.com/en/pro-app/latest/tool-reference/spatial-statistics/how-exploratory-regression-works.htm. (18 de abril de 2024).

Ferrier, S. and A. Guisán. 2006. Spatial modelling of biodiversity at the community level. Journal of Applied Ecology 43(3):393-404. Doi: 10.1111/j.1365-2664.2006.01149.x.

Fotheringham, A. S., C. Brunsdon and M. Charlton. 2002. Geographically Weighted regression: The analysis of spatially varying relationships. Wiley. Hoboken, NJ, United States of America. 284 p.

Gillespie, T. W., G. M. Foody, D. Rocchini, A. P. Giorgi and S. Saatchi. 2008. Measuring and modelling biodiversity from space. Progress in Physical Geography 32(2):203-221. Doi: 10.1177/0309133308093606.

Hernández-Stefanoni, J. L., F. Tun D., J. Andrés-Mauricio y L. Á. Hernández M. 2023. Métodos de interpolación espacial para el mapeo de la riqueza de especies usando R. Centro de Investigación Científica de Yucatán, A. C. (CICY). Mérida, Yuc., México. 191 p. https://www.cicy.mx/Documentos/CICY/Investigacion/Recursos_Naturales/Interpolacion/2023-Libro-Metodos-de-interpolacion-CICY.pdf. (26 de junio de 2024).

Hernández-Stefanoni, J. L., J. A. Gallardo-Cruz, J. A. Meave, D. Rocchini, J. Bello-Pineda and J. O. López-Martínez. 2012. Modeling α- and β-diversity in a tropical forest from remotely sensed and spatial data. International Journal of Applied Earth Observation and Geoinformation 19:359-368. Doi: 10.1016/j.jag.2012.04.002.

Instituto de Ciencias de la Atmósfera y Cambio Climático. 2009. Atlas Climático Digital de México. Universidad Nacional Autónoma de México. https://atlasclimatico.unam.mx/acdm/visualizador. (18 de abril de 2024).

Kiran, G. S. and A. Mudaliar. 2012. Remote sensing & Geo-informatics technology in evaluation of forest tree diversity. Asian Journal of Plant Science & Research 2(3):237-242. https://www.imedpub.com/articles/remote-sensing--geoinformatics-technology-in-evaluation-offorest-tree-diversity.pdf. (18 de abril de 2024).

Lande, R. 1996. Statistics and partitioning of species diversity, and similarity among multiple communities. Oikos 76(1):5-13. Doi: 10.2307/3545743.

Leija, E. G., N. P. Pavón, A. Sánchez-González, R. Rodríguez-Laguna y G. Ángeles-Pérez. 2021. Dinámica espacio-temporal de uso, cambio de uso y cobertura de suelo en la región centro de la Sierra Madre Oriental: Implicaciones para una estrategia REDD+ (Reducción de Emisiones por la Deforestación y Degradación). Revista Cartográfica 102:43-68. Doi: 10.35424/rcarto.i102.832.

Lu, B., Y. Hu, D. Murakami, C. Brunsdon, … and P. Harris. 2022. High-performance solutions of geographically weighted regression in R. Geo-spatial Information Science 25(4):536-549. Doi: 10.1080/10095020.2022.2064244.

Madonsela, S., M. A. Cho, A. Ramoelo and O. Mutanga. 2017. Remote sensing of species diversity using Landsat 8 spectral variables. ISPRS Journal of Photogrammetry and Remote Sensing 133:116-127. Doi: 10.1016/j.isprsjprs.2017.10.008.

Madonsela, S., M. A. Cho, A. Ramoelo, O. Mutanga and L. Naidoo. 2018. Estimating tree species diversity in the savannah using NDVI and woody canopy cover. International Journal of Applied Earth Observation and Geoinformation 66:106-115. Doi: 10.1016/j.jag.2017.11.005.

Magurran, A. E. 1988. Ecological diversity and its measurement. Springer-Science+Business Media, B. Y. New York, NY, United States of America. 179 p.

Mallick, J., M. K. AlMesfer, V. P. Singh, I. I. Falqi, … and N. B. Kahla. 2021. Evaluating the NDVI–Rainfall relationship in Bisha Watershed, Saudi Arabia using Non-stationary Modeling Technique. Atmosphere 12(5):593. Doi: 10.3390/atmos12050593.

Martínez-Sifuentes, A. R., J. Villanueva-Diaz, E. Crisantos de la R. y D. W. Stahle. 2021. Modelado actual y future de la idoneidad de habitat el ahuehuete (Taxodium mucronatum Ten.): una propuesta para conservación en México. Botanical Sciences 99(4):752-770. Doi: 10.17129/botsci.2772.

Meng, J., S. Li, W. Wang, Q. Liu, S. Xie and W. Ma. 2016. Estimation of forest structural diversity using the spectral and textural information derived from SPOT-5 satellite images. Remote Sensing 8(2):125. Doi: 10.3390/rs8020125.

Miller, J. 2010. Species distribution modeling. Geography Compass 4(6):490-509. Doi: 10.1111/j.1749-8198.2010.00351.x.

Nakaya, T. 2015. Geographically Weighted Generalised linear modelling. In: Brunsdon, C. and A. Singleton (Editors). Geocomputation: A practical primer. SAGE Publications, Inc. Thousand Oaks, CA, United States of America. pp. 201-220.

Nakaya, T. 2016. GWR4 user manual. Windows application for Geographically Weighted Regression modelling. Maynooth University. Kildare, L, Ireland. 39 p. https://sgsup.asu.edu/sites/default/files/SparcFiles/gwr4manual_409.pdf. (18 de mayo de 2024).

Peet, R. K. 1974. The Measurement of species diversity. Annual Review of Ecology and Systematics 5:285-307. http://www.jstor.org/stable/2096890. (18 de abril de 2024).

Rosales M., S. 2016. Reconstrucción de precipitación e incendios en bosques de coníferas en el ejido Adolfo Ruiz Cortines, Pueblo Nuevo, Durango. Tesis de Maestría en Ciencias Forestales. Facultad de Ciencias Forestales, Universidad Autónoma de Nuevo León. Linares, NL, México. 63 p.

Salami, K. D., R. B. Shuaibu, V. A. J. Adekunle and J. D. Ogunsola. 2021. Comparative analysis of density, diversity and similarity of forest tree species in three selected states of northern Nigeria. Journal of Research in Forestry, Wildlife and Environment 13(3):111-124. https://www.ajol.info/index.php/jrfwe/article/view/217258. (30 de mayo de 2024).

Sancha N., E. F. 2010. El estudio de los índices de vegetación como base para conocer las relaciones entre la vegetación y el clima. In: Ojeda Z., J., I. Vallejo V. y M. F. Pita L. (Coords.). Congreso Nacional de Tecnologías de la Información Geográfica. Editorial de la Universidad de Sevilla. Sevilla, SE, España. pp. 1095-1108.

Sánchez-Díaz, B. 2018. La teledetección en investigaciones ecológicas como apoyo a la conservación de la biodiversidad: una revisión. Revista Científica 33(3):243-253. Doi: 10.14483/23448350.13370.

Simpson, E. H. 1949. Measurement of diversity. Nature 163:688. Doi: 10.1038/163688a0.

Song, X., M. Cao, J. Li, R. L. Kitching, … and J. Yang. 2021. Different environmental factors drive tree species diversity along elevation gradients in three climatic zones in Yunnan, southern China. Plant Diversity 43(6):433-443. Doi: 10.1016/j.pld.2021.04.006.

Vargas-Larreta, B., C. A. López-Sánchez, J. J. Corral-Rivas, J. O. López-Martínez, C. G. Aguirre-Calderón and J. G. Álvarez-González. 2017. Allometric equations for estimating biomass and carbon stocks in the temperate forests of North-Western Mexico. Forests 8(8):269. Doi: 10.3390/f8080269.

Vela-Pelaez, A. A., M. A. Navarro-Martínez, M. A. Mendoza B., J. A. Sánchez-Sánchez y L. G. Esparza-Olguín. 2024. Análisis multitemporal de cambios en el NDVI en una región con aprovechamiento forestal en la península de Yucatán, México. Revista Mexicana de Ciencias Forestales 15(81):160-186. Doi: 10.29298/rmcf.v15i81.1425.

Xu, X., D. Dimitrov, N. Shrestha, C. Rahbek and Z. Wang. 2019. A consistent species richness–climate relationship for oaks across the Northern Hemisphere. Global Ecology and Biogeography 28(8):1051-1066. Doi: 10.1111/geb.12913.

 

 

 

 

        

Todos los textos publicados por la Revista Mexicana de Ciencias Forestales sin excepción– se distribuyen amparados bajo la licencia Creative Commons 4.0 Atribución-No Comercial (CC BY-NC 4.0 Internacional), que permite a terceros utilizar lo publicado siempre que mencionen la autoría del trabajo y a la primera publicación en esta revista.