Sei sulla pagina 1di 17

doi:10.21829/myb.2017.

231495
Madera y Bosques vol. 23, nm. 1: 143-159 Primavera 2017

Site index curves for natural


Aleppo pine forests in the central
Ebro valley (Spain)
Curvas de ndice de sitio para las masas naturales de pino de Aleppo en el
valle central del Ebro (Espaa)

Alberto Rojo-Alboreca1*, Ana Ma. Cabanillas-Saldaa2, Marcos Barrio-Anta3, Eduardo Notivol-Pano4 and
J. Javier Gorgoso-Varela1

1 Universidade de Santiago de Compostela. Escola Po- 2 Gobierno de Aragn. Servicio Provincial de Desarro- 4 Gobierno de Aragn. Unidad de Recursos Forestales.
litcnica Superior. Departamento de Enxeara Agro- llo Rural y Sostenibilidad. Zaragoza, Spain. acabani- CITA. Zaragoza, Spain. enotivol@aragon.es
forestal. Unidade de Xestin Forestal Sostible. Lugo, llas@aragon.es
Spain. josejavier.gorgoso@usc.es 3 Universidad de Oviedo. Escuela Politcnica de Mie-
* Corresponding author. alberto.rojo@usc.es res. Departamento de Biologa de Organismos y Sis-
temas. Mieres, Spain. barriomarcos@uniovi.es;

Abstract
Site index curves were created for natural Aleppo pine (Pinus halepensis Mill.) stands in the Ebro Valley (northeastern Spain). Data were
obtained from 54 felled dominant trees. The Generalized Algebraic Difference Approach (GADA) was used to fit 11 equations with a
longitudinal data structure that included all possible growth intervals. Three statistical criteria were used for model comparison: root
mean square error (RMSE), adjusted coefficient of determination (R2adj) and Akaikes information criterion (AIC). Graphical evaluation
of the data (plots of observed against predicted values and of residuals against predicted values) was also conducted. In addition, the
root mean square error (RMSE) was plotted against age. Finally, fitted site index curves for different site qualities were superimposed on
the profile plots of the stems analysed. The best reference age (60 years) was calculated from the relative error in the dominant height
prediction. The Hossfeld IV model proved the most suitable for representing site index in the study area. Furthermore, only three site
index curves (6 m, 10 m and 14 m at 60 years) were suitable for classifying the entire study area because of the low productivity of the
stands. These were compared with other site index curves developed for Spain and other countries, for the natural range of distribution
of the species. Specific site index curves must be created for the study area, because the existing qualities and growth patterns are not
well-represented in other models.

Key words: GADA, Hossfeld model, Pinus halepensis, productivity.

Resumen
Se han elaborado unas curvas de ndice de sitio para las masas naturales de pino de Aleppo (Pinus halepensis Mill.) del valle del Ebro (no-
reste de Espaa), a partir del anlisis de tronco de 54 rboles dominantes. Se utiliz la generalizacin de la metodologa de ecuaciones en
diferencias algebraicas (GADA por sus siglas en ingls) para ajustar un total de 11 ecuaciones. La comparacin de los modelos se realiz
mediante tres estadsticos: raz del error medio cuadrtico (RMSE), coeficiente ajustado de determinacin (R2adj) y criterio de informacin
de Akaike (AIC). Tambin se utiliz una evaluacin grfica de valores observados y residuales frente a predichos para comparar modelos,
y otra de la raz del error medio cuadrtico (RMSE) frente a la edad. Adems, las curvas ajustadas fueron superpuestas a los perfiles de
los anlisis de tronco utilizados. La mejor edad de referencia (60 aos) se calcul a partir del error relativo en la prediccin de la altura
dominante. El modelo de Hossfeld IV ofreci los mejores resultados, y solamente tres ndices de sitio (6 m, 10 m y 14 m a los 60 aos)
fueron suficientes para clasificar todas las masas, caracterizadas por su baja productividad. Finalmente, las curvas fueron comparadas
con otras existentes para la especie en Espaa y en otros pases de su rea de distribucin natural. Esta comparacin revel la necesidad
de contar con unas curvas de ndice de sitio especficas para la zona de estudio, pues las calidades y los patrones de crecimiento existentes
no estn bien representados en otros modelos.

Palabras clave: GADA, modelo de Hossfeld, Pinus halepensis, productividad.

143
Rojo-Alboreca et al. Site index curves for Aleppo pine forests in Spain

Introduction Site index curves have been developed for Pinus hale-
The productive potential of forest stands (mainly for tim- pensis in other countries within the range of distribution
ber products) and the silvicultural methods required to of the species: Italy (Castellani, Chidini and Tosi, 1980);
achieve this potential by the end of the rotation period are France (Pard, 1957; Abbas, Barbero, Loisel and Quezel,
particularly important aspects of forest management. Site 1985a; Abbas, Barbero, Loisel and Quezel,1985b; Cou-
index is commonly used as an indicator of the potential hert & Duplant, 1993; Vennetier & Herve, 1999); Greece
productivity of a forest area, and it enables site classifica- (Panetsos, 1981); Tunisia (Souleres, 1975); Argelia
tion and comparison between different sites. (Gualdi, 1979; Franz & Forster, 1980); Israel (Rhle,
Dominant height is commonly used to construct site 1992); and Morocco (Belghazi, Ezzahiri and Romane,
index curves because it is easily determined in the field, is 2000).
closely correlated with volumetric production, indicates Because all of the above mentioned works for Spain
the quality of the stand for all ages and is relatively inde- or other countries were carried out prior to the year 2000,
pendent of stand density (except at extreme values) and of none of them used the Generalized Algebraic Difference
the silvicultural treatments applied (Clutter, Fortson, Pie- Approach (GADA) proposed by Cieszewki and Bailey
naar, Brister and Bailey, 1983). Dominant height can be (2000), widely used al later times for other species to ela-
defined as the mean height of the hundred largest diame- borate site index curves (e.g. Tom, Ribeiro and Soares,
ter trees per hectare (Assmann, 1970). In the present 2001; Sharma, Amateis and Burkhart, 2002; Fontes et al.,
study, this simple, widely used definition enabled compa- 2003; Palah et al., 2003; lvarez-Gonzlez, Ruiz-Gonz-
rison of new and existing site index curves for Pinus hale- lez, Rodrguez-Soalleiro and Barrio-Anta, 2005; Barrio-
pensis (Aleppo pine). Anta & Diguez-Aranda, 2005; Diguez-Aranda,
Pinus halepensis is naturally distributed in Spain lvarez-Gonzlez, Barrio-Anta and Rojo-Alboreca,
throughout the Mediterranean area of the southeast of the 2005a; Diguez-Aranda, Burkhart and Rodrguez-Soa-
Iberian Peninsula and in the Balearic Islands (Serrada et lleiro, 2005b; Adame, Caellas, Roig and Del Rio, 2006;
al., 2008). The area occupied by natural stands of Pinus Tahar et al., 2012; Lopez-Senespleda, Bravo-Oviedo,
halepensis in Spain represents 7% of afforested land Alonso and Montero, 2014).
(Herranz, 2000), and plantations with this species repre-
sent 15% of those established between 1940 and 1980 Objectives
(Abell, 1988). However, the species is not particularly The main objective of this study was to elaborate site
productive relative to other pines. Scant attention has the- index curves for natural even-aged stands of Pinus hale-
refore been given to Aleppo pine, even though on a local pensis Mill. in two large areas of the Ebro valley (Spain)
scale it may be the only economic alternative available and using the GADA methodology, in order to improve esti-
may complement other non-timber harvests. mate of dominant height growth and to compare the refe-
In Spain, site index curves have been developed for rence age and range of the fitted curves with those of the
Pinus halepensis in four different studies (Pita, 1965; Erviti, existing models for the species.
1991; Montero, Grau, Ruiz-Peinado, Ortega and Caellas,
2000; Montero, Caellas and Ruiz-Peinado, 2001), although Materials and Methods
the origin (natural regeneration or plantation) was not indi-
cated in any of these. The productivity of Pinus halepensis in Data set
Spain was investigated many years ago by Martn-Bolaos The study was conducted in an area of approximately
(1947), who quantified productivity in four contemporary 40 000 ha in the central Ebro valley (which includes parts
plantations but did not establish site index classes. of the provinces of Zaragoza and Huesca, in northeast

144
Madera y Bosques vol. 23, nm. 1: 143-159 Primavera 2017

Table 1. Summary of the main dominant tree variables from


the sample used to fit the site index curves.

Statistics h d h/d vob vub t


Minimum 4.89 13.37 27 0.02 0.02 42
Maximum 16.03 47.75 49 1.05 0.83 117
Mean 10.20 28.13 38 0.34 0.27 76.23
Standard deviation 3.15 8.37 0.05 0.27 0.22 19.84

Where h: total height (m); d: diameter at breast height (cm); vob: over bark stem
volume (dm3); vub: under bark stem volume (dm3); t: age (years).

Figure 1. Map showing the study area.


Figure 2 shows the temporal changes in height of each of
the dominant trees used in the fits and the curve corres-
Spain) where Pinus halepensis is naturally distributed ponding to the mean values for each age (thick line). This
(Fig. 1). The area encompasses more than 80% of the total type of graph is of great help in diagnosing the mean
area of distribution of the Monegros-Ebro valley Prove- structure of a population, as it indicates whether there is a
nance of the species (Gil et al., 1996). lack or scarcity of data in some zones. A step-wise decrease
Data used to develop the site index curves come from to midline data after 72 years was observed (although the
stem analysis of 54 felled dominant trees, ranged across overall trend was maintained). This was due to the scar-
all existing site qualities in the area. city of data for older ages and was more evident in the
The 54 felled trees were cut into 1 m sections, and the better quality stands. This is a common problem in deve-
total height of the tree (m), length of the sections (m), loping site index curves for forest species with interme-
height of the stump (cm), perimeter (m), bark thickness diate and long rotations, which often do not include data
(two measurements at right angles, mm) and number of from high quality stands of advanced ages.
rings were recorded (the latter three parameters were mea- In this study, site index was represented by the
sured in each section). The number of rings was visually height of the dominant trees, measured according to
counted in the field, taking into account the possibility of
existence of false or double rings in this species (Novak,
Luis, ufarc and Ravents, 2011). The total volumes with
and without bark were estimated by Smalians formula,
except for the top section, which assumes the form of a
cone. The descriptive statistics of the main variables from
the sample of trees used for fitting the site index curves are
shown in Table 1.
To eliminate the skew introduced in stem analysis
when estimating the real age at which the felling height is
reached in the stem (given that the felling section does not
coincide with periodic growth in height), the method of Figure 2. Mean structure (thick line) of the data used to develop
Carmean (1972), with the modification proposed by New- the site index equations superimposed on the profile plots of the
berry (1991), was used for the top section. 54 stem analyses.

145
Rojo-Alboreca et al. Site index curves for Aleppo pine forests in Spain

the definition given by Assmann (1970), at a certain The dynamic equations in the form of algebraic diffe-
indicator or reference age (Carmean, 1970). The refe- rences are based on the height Y at age t, for which the
rence age usually coincides with the culmination of following three parameters must be known: height Y0 at a
mean increment, or two thirds or the rotation for a previous age t 0 and ages t 0 and t, i.e. Y = f(t, Y0 , t 0).
stand of intermediate quality (Pita, 1991). Pita (1965) The final expression is obtained after resolving some
and Erviti (1991) established the reference age for of the model parameters on the basis of t 0, Y0 and the
Pinus halepensis as 40 years, but more recently Mon- other parameters, and then substituting these in the model
tero et al. (2000; 2001) considered a reference age of to express Y as a function of Y0, t 0, t and the other para-
80 years. We selected the reference age by first calcula- meters (Ramrez-Maldonado, Bailey and Dorders, 1988).
ting the error associated with the dominant height and In dynamic equations in which two parameters are related
then searching for the reference age that many trees to site, these must be reparameterized by considering that
have reached but that minimizes the aforementioned each depends on an unknown site characteristic, so that a
error. mathematical solution can be found.
These models require longitudinal data from perma-
Base models nent plots in which two or more measurements corres-
We used the Generalized Algebraic Difference Approach pond to the same stand (Gadow and Hui, 1999), or stem
(GADA) proposed by Cieszewki and Bailey (2000) with analysis data. Six different data structures can be genera-
longitudinal data from stem analysis that considers all ted from stem analysis data for use in fitting models
possible growth intervals. This method is a generalization expressed as algebraic difference equations. However, the
of the method based on algebraic differences (Algebraic data structure that includes all possible growth intervals
Difference Approach, ADA) developed by Bailey and also provides the most stable and consistent results (Goelz
Clutter (1974). and Burk, 1992; Huang, 1999), and this type of structure
In the ADA method, dynamic equations that relate was therefore used in the present study.
dominant height and age are obtained. The main advan- The fitted models are shown in table 2, along with
tage of the GADA method is that the dynamic equations the original model and the parameter related to site.
are obtained from the same base equation as the ADA Equations CC1, CC2 and CC3 were formulated from
models, but allow more than one parameter to be depen- the integral form of the base equation of Bertalanffy-
dent on the forest site, thus enabling development of more Richards (Bertalanffy, 1949; 1957; Richards, 1959). The
flexible equations. first two of these were obtained by expressing the base
The dominant height growth equations selected were equation in algebraic differences and resolving a3 in the
those that generate polymorphic curves (Clutter et al., first case and a2 in the second case. Equation CC3 is the
1983). These curves are also denominated non proportio- result of relating parameters a1 and a3 to site, according to
nal because they do not display a proportional relations- the expressions in table 2. The first two solutions were
hip between the values of the dominant height, and each used in several studies involving modelling of the domi-
curve therefore takes a different form. nant height growth of several forest species in the Iberian
The selected models are derived from several base Peninsula (e.g. Fontes et al., 2003; Palah, Tom, Pukkala,
growth equations expressed in difference algebraic forms. Trasobares and Montero, 2003; lvarez-Gonzlez et al.,
These models generated all possible polymorphic solu- 2005; Barrio-Anta and Diguez-Aranda, 2005; Diguez-
tions that relate a single parameter to site. Polymorphic Aranda et al., 2005a; b). The dynamic model obtained by
solutions that related two parameters to site were also relating two parameters to site (equation 3) was also used
obtained for three of the models. to model dominant height growth of Pinus taeda in Geor-

146
Madera y Bosques vol. 23, nm. 1: 143-159 Primavera 2017

gia (USA) with the aim of testing different fitting methods used in Spain to elaborate site quality curves for different
(Cieszewski, Harrison and Martin, 2000). This model species (Pita, 1964; 1965; 1966), and the polymorphic
also produced the best results for Quercus faginea in solution used in the present study was the same model
Spain (Lopez-Senespleda et al., 2014). chosen for elaborating site index curves for Pinus sylves-
Equations CC4, CC5 and CC6 are polymorphic tris in northeastern Spain (Palah et al., 2003).
forms of the base model of Korf (Lundqvist, 1957), which The dynamic equations CC9 and CC10 were develo-
is usually referred to as the model of Bailey and Clutter ped from the Hossfeld IV equation (Kiviste et al., 2002).
(1974) or of Schumacher (1939). The first two models are Models derived from this equation have frequently been
obtained from the base equation expressed as algebraic used to describe a wide range of population dynamics (e.g.
differences and resolving parameters b1 and b 2 respecti- Monserud, 1988; Cieszewski, 2000; 2001; 2002; 2003).
vely. The third equation (CC6) is obtained by relating The expression of the first model (CC9) is a special solu-
parameters b 0 and b1 to the site according to the expres- tion proposed by Cieszewski and Bella (1989) and was
sion indicated in table 2. The first two models have often used to elaborate site index curves for Pinus sylvestris in
been used to model dominant height growth (e.g. Tom et Sweden (Elfving and Kiviste, 1997). This model also pro-
al., 2001; Fontes et al., 2003; Palah et al., 2003; lvarez- duced some of the best results in studies by Corral-Rivas
Gonzlez et al., 2005; Barrio-Anta and Diguez-Aranda, et al. (2004), Barrio-Anta and Diguez-Aranda (2005)
2005; Diguez-Aranda et al., 2005a). Of these two poly- and Diguez-Aranda et al. (2005a; b). The next model
morphic solutions, model CC4 provided the best results (CC10) is a special solution of the Hossfeld IV equation,
and was selected by Tom et al. (2001) and by Barrio- proposed by Cieszewski (2002).
Anta and Diguez-Aranda (2005) to construct site quality The final model used (CC11) is the equation propo-
curves for respectively Eucalyptus globulus in Portugal sed by McDill and Amateis (1992), expressed as algebraic
and Quercus robur in Galicia (NW Spain). Model CC6 differences, and resolved for parameter a 2 . This model has
was used by Barrio-Anta et al. (2005) to develop a basal been successfully applied in several studies to model height
area growth model for Pinus pinaster stands in Galicia, growth (e.g. Sharma et al., 2002; Fontes et al., 2003; Di-
and also by Tahar et al. (2012) and Vargas-Larreta, Agui- guez-Aranda et al. 2005a).
rre-Caldern, Corral-Rivas, Crecente-Campo and Die-
guez-Aranda (2013) to develop dominant height growth Fitting method
models for Pinus pinea in Tunisia and for Pinus pseudos- The data used consist of several observations of the height
trobus in Mexico respectively. over time for each of the trees (so-called longitudinal
Dynamic equation CC7 is a polymorphic solution of data). These longitudinal data were transformed to gene-
the base equation of Sloboda (1971) and has been tested in rate a structure that considers all possible growth inter-
Galicia for Quercus robur (Barrio-Anta and Diguez- vals among height-age pairs for each tree.
Aranda, 2005) and for Pinus sylvestris (Diguez-Aranda One of the most important problems when fitting
et al., 2005a); in both cases it was one of the models that regression equations to model height growth is the tem-
produced the best results. It has also been tested with five poral dependence or autocorrelation between measure-
species of pine in Mexico (Corral-Rivas, lvarez-Gonz- ments. The autocorrelation between errors, inherent in
lez, Ruiz-Gonzlez and Gadow, 2004). data from permanent plots or from stem analysis, was
Model CC8 is the solution for parameter a2 of the corrected by use of the non linear generalized least-squa-
base model of Hossfeld (1822, described in Kiviste, lva- res method and by modelling the error structure with a
rez-Gonzlez, Rojo-Alboreca and Ruiz-Gonzlez, 2002) first order autoregressive model (AR1). For this purpose,
expressed as an algebraic difference. This base model was simultaneous fitting of the mean structure (dynamic

147
148
Table 2. Models used to fit the site index curves: Y= f(Y0, t 0, t). (Part 1/2).

Equation Site-related Solution for X with initial values (t0, Y0) Dynamic equation
parameter
Bertalanffy-Richards (Bertalanffy,
1949, 1957; Richards, 1959)
ln (1 exp ( b1t ))
a
Y = a1 (1 exp( a 2 t )) 3 ln (Y0 b 1 ) Y ln (1exp (b1t0 ))
X0 = CC1
ln (1 exp ( b 2 t 0 ))
a3 = X Y = b0 0
b0
b3

1 b3
Y 1 b3 t t0
a2 = X X 0 = ln 1 (Y0 b1 )
( )t 0 Y = b1 1 1 0 CC2
b
1

2
a1 = exp( X ) X 0 = 12 (ln Y0 b2 L0 ) (ln Y0 b2 L0 ) 4b3 L0
( ) ( b2 + b3 X 0 )
1 exp( b1t )
Y = Y0 CC3
a3 = b2 + b3 X L0 = ln(1 exp( b1t0 )) 1 exp( b1t0 )
with
Korf (Lundqvist, 1957) b3
t0
Y a3 Y t
1
a2 = X X 0 = ln 0 t 0 CC4
(
Y = a1 exp a 2 t a 3 ) a1
Y = b1 0
b1
ln ( Y0 b0 )

ln b1 ln t0
ln (Y0 a1 )
a3 = X X 0 = ln ln (t 0 )
Y = b0 exp b1t CC5

a2

a1 = exp( X ) 2
b3 b b b
X 0 = 12 t 0 (
b1 + t 0 3 ln (Y0 ) 4b2 t 0 3 + b1 t 0 3 ln (Y0 ) ) (
Y = exp ( X 0 ) exp (b1 + b2 X 0 )t b 3 ) CC6

a 2 = b1 + b2 X
Sloboda (1971)
b2 b2
exp
ln (Y0 a1 ) (b 1)t ( b3 1 ) (b 1)t ( b3 1 )
Y 3 3 0
a3 a2 = X X0 = ( a4 1) CC7
Y = a1 exp a 2 exp exp a3 (a 4 1)t 0
( ) Y = b0 0
(a 1)t ( a 4 1) b0
4
Rojo-Alboreca et al. Site index curves for Aleppo pine forests in Spain
Table 2. Models used to fit the site index curves: Y= f(Y0, t 0, t). (Part 2/2).

Equation Site-related Solution for X with initial values (t0, Y0) Dynamic equation
parameter

Hossfeld I (Kiviste et al., 2002)


Madera y Bosques

t2
t a Y=
t2 a2 = X X 0 = 0 1 a3 t 0 t b CC8
Y= Y0 t 0 b1 + t 0 1 + b3 (t t 0 )
a1 + a 2 t + a3t 2 Y0 t 0
Hossfeld IV (Kiviste et al., 2002) Y0 + d + r
Y=
a1 = X t b2
2 + 4b3
(Y0 d + r )
assuming a3
CC9
vol. 23, nm. 1: 143-159

a1
(
X 0 = Y0 1 + (a 4 S ) t 0 ) b2
Y= a4
with
d = b3 Asi
1 + a 2 t a3 a2 =
S
2
and r= (Y0 d )2 + 4b3Y0t0 b
a1 = b1 + X b1 + X 0
1 3
Primavera 2017

X0 = 2 0
(Y b 1 (Y0 b1 )2 + 4b2Y0t0b ) Y= CC10
1 + b2 X 0 t b3
a2 = b2 X
McDill-Amateis (1992)
b0
a1 a a Y= b
Y= a3 = X X 0 = 1 1t 0 2 b t 1 CC11
1 + a 3 t a2 Y0 1 + 0 1 0
Y0 t

Where Y: dominant height (m) at age t; Y0: dominant height (m) at age t0; S: site index at the reference age; Asi: reference age; ln: natural logarithm; exp: exponential
function; b0, b1, b2 and b3: parameters to be estimated.

149
Rojo-Alboreca et al. Site index curves for Aleppo pine forests in Spain

structure) and the error structure (autoregressive model) the residual ij and the independent variables are the resi-
was carried out by use of the MODEL procedure in the duals i-1, j and i, j-1; and (v) fitting the mean (obtained from
SAS/ETS program (SAS Institute Inc., 2001), which the growth equation) and the error structure (obtained
enables dynamic updating of the residuals (Parresol and from the autoregressive model) simultaneously by the
Vissage, 1998). MODEL procedure of SAS/ETS (SAS Institute Inc., 2001),
The data structure used in the present study included with the values of the parameters obtained in steps (ii) and
all possible growth intervals. In this case, the error struc- (iv) as initiators of the regression analysis.
ture should be expressed as indicated in equation 1, in
accordance with Goelz and Burk (1992). Model evaluation
Comparison of the fitted models was based on numerical
Yij = f ( X i , Y j , X j , ) + ij (Equation 1) and graphical analyses. Three statistical criteria obtained
from the residuals were examined: (i) the root mean square
with: ij = i 1, j + i , j 1 + eij error (RMSE), which analyses the accuracy of the estima-
tes; (ii) the adjusted coefficient of determination (R 2adj),
and where Yij represents the prediction of the height i which shows the proportion of the total variance that is
from height j (Yj), age i (Xi), and age j (Xj with ji); is the explained by the model, adjusted for the number of model
vector of parameters to be estimated; ij represents the parameters and the number of observations; and (iii)
error under the condition of non independence; the para- Akaikes information criterion (AIC), which is an index
meter represents the autocorrelation between the actual used to select the best model on the basis of minimizing
residual (corresponding to the Yij estimate) and the resi- the Kullback-Liebler distance (Burnham and Anderson,
dual corresponding to the Yi-1 estimate obtained with Yj as 1998). These criteria are summarized in equations 2, 3
the predictor variable; parameter represents the relation and 4 respectively.
between the actual residual and the residual of the esti-
mate of Yi with Yj-1 as the predictor variable; and eij repre- n 2

sents the stochastic error of the model eij N(0,), ( yi yi )


independently and identically distributed. RMSE = i=1
(Equation 2)
In the definitive expression of the models, the values
n p
of the parameters of the structure of the autocorrelation n

(y y i )
2
error are ignored, as the main purpose of their use is to i
2 i =1 n 1
obtain an unskewed more accurate estimate of the Radj
= 1 n (Equation 3)
2 n p
parameters of the mean structure (dynamic model). (y
i =1
i yi )
Moreover, in practice, the values of errors i-1 and i-2
cannot be determined without stem analysis (Monserud,
1984). AIC = n log 2 + 2 k (Equation 4)
In summary, the process used to fit autoregressive
GADA models with all possible growth intervals consis- where yi , yi and yi are the measured, predicted and
ted of the following steps: (i) determination of all possible mean values of the dependent variable, respectively; n is
growth intervals between the height-age pairs for each the total number of observations used to fit the model; p is
tree; (ii) fitting the model without considering the error the number of model parameters; k = p + 1; and 2 is the
structure; (iii) determination of the errors ij , i-1,j and i,j-1; estimator of the error variance of the model obtained with
(iv) fitting a linear model in which the dependent model is Equation 5.

150
Madera y Bosques vol. 23, nm. 1: 143-159 Primavera 2017

N 2
Results
( yi yi )
(Equation 5) The fitting results, parameter values and standard errors
i =1
2 = are shown in table 3. All parameters were significant at a
n
significance level of 5%.
In addition to these three statistics, one of the most The values of the comparative statistics for the eleven
efficient ways of comparing models is visual inspection dynamic models are shown in table 4. The models were
of graphs to detect any possible systematic discrepancies. fitted by considering a first-order autoregressive structure
Plots of observed against predicted values of the depen- for the errors and were fitted to a data structure that
dent variable and plots of studentized residuals against includes all possible growth intervals.
the predicted dominant height were therefore examined. The model that best fit the data was model CC3,
The variations in RMSE with age (ranged in age classes followed by models CC10, CC11, CC2 and CC9, which
of five years intervals) were also plotted for each of the all provided similar fits.
analysed models. The changes in the RMSE were plotted against age
Graphs of the fitted curves overlaid on the trajecto- (ranged in five-year age classes) for all eleven models
ries of the stem analysis were also examined. The curves analysed as shown in figure 3, in which it can be seen that
estimated from the model must be demonstrated to fit the the models with the lowest RMSE for almost all age clas-
real tree profiles. Moreover, curves for which the compa- ses were CC9, CC11, CC10 and CC2.
rative statistics are identical may have very different gra- The reference age considered was 60 years. As
phical appearances (Huang, 1999). already explained, this was selected by first calculating

Figure 3. Plot of variations in RMSE in relation to age (age ranged in five-year age classes: age class 1: 6 years - 10 years; age class 2:
11years - 15 years, ) for the 11 models under study.

151
Rojo-Alboreca et al. Site index curves for Aleppo pine forests in Spain

Table 3. Values of the parameters and standard errors for the different models.

Model Parameter Value Standard error Model Parameter Value Standard error
CC1 b0 44.2323 0.7000 CC7 b0 72.5217 1.8197
b1 0.0041 0.0001 b1 0.2256 0.0015
-0.9054 0.0042 b2 0.8596 0.0033
-0.1494 0.0038 -0.9219 0.0038
CC2 b1 18.6659 0.0720 -0.1324 0.0034
b3 1.3126 0.0025 CC8 b1 8.2775 0.1047
-0.9270 0.0036 b3 0.0202 0.0002
-0.1330 0.0032 -0.9527 0.0035

CC3 b1 0.0163 0.0001 -0.1105 0.0032

b2 -0.8079 0.0381 CC9 b2 1.3097 0.0024

b3 6.1171 0.1094 b3 2.046.3110 8.7046


-0.9164 0.0038 -0.9305 0.0035
-0.1379 0.0034 -0.1271 0.0032

CC4 b1 319.3027 11.1119 CC10 b1 21.2343 0.2963

b3 0.2941 0.0019 b2 607.3497 65.6256


-0.9367 0.0035 b3 1.3141 0.0025
-0.1194 0.0032 -0.9286 0.0036

CC5 b0 129.6093 3.0451 -0.1280 0.0032

b1 8.1345 0.0143 CC11 b0 24.2616 0.1249


-0.9872 0.0030 b1 1.3013 0.0023
-0.0808 0.0027 -0.9275 0.0036

CC6 b1 0.0036 0.0020 -0.1294 0.0032

b2 62.3206 0.7127
b3 0.1931 0.0018
-0.9442 0.0035 number of trees reaching major reference ages is signi-
ficantly reduced.
-0.1173 0.0031
The fitted models were plotted in the graphs of the
tree profiles used in the fits. The graphic appearance of
some models varied somewhat with respect to others,
the relative error (RE, %) associated with the domi- even when the comparative statistics were quite similar, as
nant height and searching for the reference age that reported by Huang (1999). After inspection of the graphs,
many trees (n, number of observations) have reached we found that models CC9 and CC10 provided the best
but that minimizes the aforementioned error for the fit- fits to the trends in the tree data profiles. Adequate values
ted models (Fig. 4). As shown in figure 4, a large num- of the statistics used to compare the models were also
ber of trees (n) have reached the age of 60 years to obtained for the latter models. Comparison of the curves
which ER has a reasonable value close to 15%. At obtained with both equations (Fig. 5) revealed that model
lower reference ages ER increases noticeably, while the CC10 slightly overestimated the values of the best quali-

152
Madera y Bosques vol. 23, nm. 1: 143-159 Primavera 2017

Table 4.Values of the statistics used to compare the different


models.

Model RMSE R2adj AIC


CC1 0.613 0.976 -34,501.58
CC2 0.538 0.981 -43,691.58
CC3 0.530 0.982 -44,798.77
CC4 0.572 0.979 -39,446.82
CC5 0.776 0.961 -17,924.35
CC6 0.608 0.976 -35,137.54
CC7 0.556 0.980 -41,463.35 Figure 4. Plot of relative error of dominant height (RE, %) and

CC8 0.634 0.974 -32,110.65 number of trees that have reached a certain age (n, number of

CC9 0.541 0.981 -43,385.42 observations) against age in site index prediction related to
choice of reference age for the selected model.
CC10 0.536 0.981 -43,960.69
CC11 0.538 0.981 -43,722.19

(a) (b)

Figure 5 (a and b). Graphic comparison of the site quality curves elaborated from models CC9 and CC10 superimposed on the tree
profile plots.

ties at young ages (which is not the case with the model models tested (Fig. 5), we chose dynamic equation CC9
CC9), although at more advanced ages both curves fit (Hossfeld IV, described in Kiviste et al., 2002) to represent
quite well to the trends in the data. the site index curves of Pinus halepensis in the study area,
due to its better fit to the trend of the data. In addition to
Discussion being polymorphic and presenting multiple asymptotes,
After analysis of the statistics used to compare the models this model is parsimonious (it has only two parameters).
(Table 4) and the behaviour of the RMSE per age class As above mentioned, the selected model also produ-
(Fig. 3) and graphically plotting the curves for each of the ced some of the best results in other similar studies, like

153
Rojo-Alboreca et al. Site index curves for Aleppo pine forests in Spain

those by Corral-Rivas et al. (2004) for five Mexican pine and they were compared with other site index models
species, Barrio-Anta and Diguez-Aranda (2005) for already developed for the species in other parts of Spain
pedunculate oak (Quercus robur L.) in Northwest Spain, by Pita (1965), Erviti (1991) and Montero et al. (2000,
and Diguez-Aranda et al. (2005a; b) for Pinus sylvestris 2001). The curves were also compared with those elabora-
and P. radiata plantations in Northwest Spain respectively. ted by Franz and Forster (1980) and Vennetier and Herve
The reference age established in this study was 60 (1999) for the species in Argelia and France, respectively.
years. This result contrast with those of Pita (1965) and Thus, the curves elaborated by the previously mentioned
Erviti (1991), who established the reference age for Pinus authors were superimposed on the graphical profiles of
halepensis as 40 years, and more recently Montero et al. the sample of trees used in the present study and the cur-
(2000; 2001) considered a reference age of 80 years. ves from the selected model (Fig. 7).
The selected curves were superimposed on the profi- Among existing curves for the species in Spain, those
les of the trees considered (Fig. 6). The proposed curves elaborated by Pita (1965) provided the best fits for the
(thick lines) represent the mean values of the quality data used in the present study, although the highest qua-
bands shown in different colours. As observed, three lity was much higher than that observed in the forests
qualities (6 m, 10 m and 14 m dominant height at 60 under study. In the curves elaborated by Erviti (1991) and
years) are sufficient to classify the natural Pinus halepen- by Montero et al. (2000, 2001) the site qualities were
sis forests in the area into quality classes. much higher than those observed in the present study, and
The site index curves developed for Pinus halepensis no curves corresponded to the low qualities of the forests
in this study are valid for a large area of the Ebro valley, under study.

Figure 6. Site index curves for natural Pinus halepensis Mill. stands in the central Ebro Valley (Spain) superimposed on the profile
plots for the trees considered in the study. The curves represent the mean quality of each of the coloured bands.

154
Madera y Bosques vol. 23, nm. 1: 143-159 Primavera 2017

Figure 7 (a, b, c, d and e). Plots showing the comparison between the site index curves (model CC9 for heights of 6 m, 10 m and 14
m at 60 years) and other curves for the same species, superimposed on the tree profile plots.

The first conclusion that we reached was therefore of 14 and 17 as the authors considered that these were
that the curves developed by Erviti (1991) do not define the most common in Spain. However, this does not
the whole range of qualities of the species in Spain, par- appear to be the case with the forest under study. Mon-
ticularly the lower qualities. The same also applies to tero et al. (2000; 2001) compared their curves with
the curves developed by Montero et al. (2000; 2001), those developed by Pita (1965) and showed that the first
because although four curves were established for domi- three site qualities were similar, but noted that they con-
nant heights of 11 m, 14 m, 17 m and 20 m at 80 years, sidered a site quality value of 11 rather than that of 7
the related yield tables only included site quality values considered by Pita (1965).

155
Rojo-Alboreca et al. Site index curves for Aleppo pine forests in Spain

H1 + 16.3229 + ( H1 16.3229) 2 + 8,185.244 H1 t11.3097


H2 = 1.3097 (Equation 6)
t2
2 + 8,185.244
( H1 16.3229 + ( H1 16.3229) 2 + 8,185.244 H1 t11.3097 )

where H 2 and H1 are the dominant heights (m) at ages t 2 and t1, respectively.

Regarding the curves for other Mediterranean study area presented in this work, because the existing
regions, those developed for Algeria (Franz and Forster, qualities and growth patterns in the central Ebro valley
1980) cover a similar range of site qualities as observed in are not well-represented in other models.
the present study and also adapted fairly well to the tree
profiles. References
The curves for the species in France (Vennetier and Abbas, H., Barbero, M., Loisel, R. and Quezel, P. (1985a). The
Herve, 1999) showed higher site qualities than those Aleppo pine forests in Mediterranean south-eastern
observed in the Ebro valley, as indicated by the curves France. Ecodendrometric analyses. Part 1. Foret Medite-
elaborated by Erviti (1991). rraneenne, 7(1), 35-42, 105, 110-112.
Moreover, in many cases the models developed here Abbas, H., Barbero, M., Loisel, R. and Quezel, P. (1985b). The
intersect with previously existing models, indicating diffe- Aleppo pine forests in Mediterranean south-eastern
rent growth patterns. The models proposed by Pita (1965) France. Ecodendrometric analyses. Part 2. Foret Medite-
and Vennetier and Herve (1999) show the most similar rraneenne, 7(2), 123-130, 198-200.
growth patterns to those indicated by the site index curves Abell, M. A. (1988). Historia y evolucin de las repoblaciones
developed in the present study. forestales en Espaa. Coleccin Tesis Doctorales, 126/88.
Finally, it must be mentioned that the site index cur- Madrid, Espaa: Editorial de la Universidad Complutense
ves presented in this work were included in a static growth de Madrid.
model for the species in the central Ebro valley (Cabani- Adame, P., Caellas, I., Roig, S. and Del Rio, M. (2006). Mode-
llas, 2010). lling dominant height growth and site index curves for
rebollo oak (Quercus pyrenaicaWilld.). Annals of Forest
Conclusions Science, 63, 929-940.
Site index curves for natural Pinus halepensis stands in lvarez-Gonzlez, J. G., Ruiz-Gonzlez, A. D., Rodrguez-Soa-
the central Ebro valley are presented. The selected model lleiro, R. and Barrio-Anta, M. (2005). Ecoregional site
is Hossfeld IV (CC9), Kiviste et al. (2002). The final index models for Pinus pinaster in Galicia (Northwestern
expression of the model is shown in equation 6. Spain). Annals of Forest Science, 62, 1-13.
The tree site qualities established are defined by Assmann, E. (1970). The principles of forest yields study.
dominant heights of 6 m, 10 m and 14 m at 60 years and Oxford, Reino Unido: Pergamon Press.
are suitable for classifying the rather unproductive forests Bailey, R. L. and Clutter, J. L. (1974). Base-age polymorphic site
in the study area. curves. Forest Science, 20, 155-159.
The curves developed in the present study are compa- Barrio-Anta, M. and Diguez-Aranda, U. (2005). Site quality of
red with existing site index models for the species in other pedunculate oak (Quercus robur L.) stands in Galicia
parts of Spain and the Mediterranean area. This revealed (northwest Spain). European Journal of Forest Research,
the need to develop the specific site index curves for the 124, 19-28.

156
Madera y Bosques vol. 23, nm. 1: 143-159 Primavera 2017

Barrio-Anta, M., Castedo-Dorado, F., Diguez-Aranda, U., Cieszewski, C. J. (2003). Developing a well-behaved dynamic
lvarez-Gonzlez, J. G., Parresol, B. R. and Rodrguez- site equation using a modified Hossfeld IV function Y3 =
Soalleiro, R. (2005). Development of a basal area growth (axm)/(c + xm-1), a simplified mixed-model and scant sub-
system for maritime pine in northwestern Spain using the alpine fir data. Forest Science, 49(4), 539-554.
GADA approach. Canadian Journal of Forest Research, Cieszewski, C. J. and Bailey, R. L. (2000). Generalized alge-
36(6), 1461-1474. braic difference approach: theory based derivation of
Belghazi, B., Ezzahiri, M. and Romane, F. (2000). Productivity dynamic site equations with polymorphism and variable
of natural stands of Aleppo pine (Pinus halepensis Miller) asymptotes. Forest Science, 46(1), 116-126.
in the Tamga forest (High Atlas, Morocco). Cahiers Agri- Cieszewski, C. J. and Bella, I. E. (1989). Polymorphic height and
cultures, 9(1), 39-46. site index curves for lodge pole pine in Alberta. Canadian
Bertalanffy, L. v. (1949). Problems of organic growth. Nature, Journal of Forest Research, 19, 1151-1160.
163(4135), 156-158. Cieszewski, C. J., Harrison, M. and Martin, S. W. (2000). Prac-
Bertalanffy, L. v. (1957). Quantitative laws in metabolism and tical methods for estimating non-biased parameters in
growth. The Quarterly Review of Biology, 32, 217-231. self-referencing growth and yield models. (Technical
Burnham, K. P. and Anderson, D. R. (1998). Model selection Report 2000-7). Athens, Georgia, USA: University of
and multimodel inference: A practical information-theo- Georgia.
retic approach. New York, USA: Springer-Verlag. Clutter, J. L., Fortson, J. C., Pienaar, L. V., Brister, H. G. and
Cabanillas, A. (2010). Bases para la gestin de masas naturales Bailey, R. L. (1983). Timber management: a quantitative
de Pinus halepensis Mill. en el Valle del Ebro. Disertacin approach. New York, USA: John Wiley & Sons. Inc.
doctoral no publicada, Universidad Politcnica de Madrid, Corral-Rivas, J. J., lvarez-Gonzlez, J. G., Ruiz-Gonzlez, A.
Madrid, Espaa. D. and Gadow, K. v. (2004). Compatible height and site
Carmean, W. H. (1970). Tree heightgrowth patterns in rela- index models for five pine species in El Salto, Durango
tion to soil and site. In C. T. Youngberg and C. B. Davey (Mexico). Forest Ecology and Management, 201, 145-160.
(Eds.), Tree growth and forest soils (499-512), Corvallis, Couhert, B. and Duplat, P. (1993). Le Pin dAlep. En Recontre
USA: Oregon State University Press. Forestiers-Chercheurs en Fort Mditerrane. La Grande
Carmean, W. H. (1972). Site index curves for upland oaks in Motte, 6-7 October 1993. Les Coloques, 63, 12-147.
central States. Forest Science, 18, 109-120. Diguez-Aranda, U., lvarez-Gonzlez, J. G., Barrio-Anta, M.
Castellani, C., Ghidini, G. and Tosi, V. (1980). Tavole dendro- and Rojo-Alboreca, A. (2005a). Site quality equations for
metriche ed alsometrica del pino dAleppo (Pinus hale- Pinus sylvestris L. plantations in Galicia (north-western
pensis Mill.) valevoli in Italia. Annali dellIstituto Spain). Annals of Forest Science, 62, 1-10.
Sperimentale per lAssestamento Forestale e per Diguez-Aranda, U., Burkhart, H. E. and Rodrguez-Soalleiro,
lAlpicoltura, 8, 3-44. R. (2005b). Modeling dominant height growth of radiata
Cieszewski, C. J. (2000). Analytical solution to the generalized pine (Pinus radiata D. Don) plantations in north-western
log-logistic equation. Forest Science, 46, 291-296. Spain. Forest Ecology and Management, 215(1-3), 271-
Cieszewski, C. J. (2001). Three methods of deriving advanced 284.
dynamic site equations demonstrated on inland Douglas- Elfving, B. and Kiviste, A. (1997). Construction of site index
fir site curves. Canadian Journal of Forest Research, 31, equations for Pinus sylvestris L. using permanent plot
165-173. data in Sweden. Forest Ecology and Management, 98,
Cieszewski, C. J. (2002). Comparing fixed and variable base- 125-134.
age site equations having single versus multiple asympto- Erviti, J. J. (1991). Desarrollo de modelos de crecimiento y pro-
tes. Forest Science, 48(1), 7-23. duccin de las masas forestales de Pinus halepensis Mill.

157
Rojo-Alboreca et al. Site index curves for Aleppo pine forests in Spain

en Espaa. Disertacin doctoral no publicada, Universi- GADA approach for Quercus faginea Lam. in Spain.
dad Politcnica de Madrid, Madrid, Espaa. Forest Systems, 23(3), 494-499.
Fontes, L., Tom, M., Coelho, M. B., Wright, H., Luis, J. S. and Lundqvist, B. (1957). On height growth in cultivated stands of
Savill, P. (2003). Modelling dominant height growth of pine and spruce in Northern Sweden. Meddelanden Fran
Douglas-fir (Pseudotsuga mensiesii (Mirb) Franco) in Statens Skogsforskningsinstitut, 47(2), 1-64.
Portugal. Forestry, 76(5), 509-523. Martn-Bolaos, M. (1947). Ensayo de investigacin indirecta
Franz, F. and Forster, H. (1980). Table de production de pin sobre origen, desarrollo y producciones del monte alto.
dAlep pour les Aurs - Algeria. Bonn, Germany: Chaire Madrid, Espaa: Instituto Forestal de Investigaciones y
de la Production Forestire de lUniversit de Munich. Experiencias.
Gadow, K. v. and Hui, G. (1999). Modelling Forest Develop- McDill, M. E and Amateis, R. L. (1992). Measuring forest site
ment. Dordrecht, The Netherlands: Kluwer Academic quality using the parameters of a dimensionally compa-
Publishers. tible height growth function. Forest Science, 38, 409-
Gil, L., Daz-Fernndez, P. M., Jimnez, M. P., Roldn, M., 429.
Ala, R., Agndez, D., De Miguel, J., Martn, S. and De Monserud, R. A. (1984). Height growth and site index curves
Tuero, M. (1996). Las regiones de procedencia de Pinus for inland Douglas-fir based on stem analysis data and
halepensis Mill. en Espaa. Madrid, Espaa: Organismo forest habitat type. Forest Science, 30, 943-965.
Autnomo Parques Nacionales. Monserud, R. A. (1988). Variations on a theme of site index. In
Goelz, J. C. G. and Burk, T. E. (1992). Development of a well- A. R. Ek, S. R. Shifley and T. E. Burk (Ed). Proceedings
behaved site index equation: jack pine in north central Onta- IUFRO conference on forest growth modelling and pre-
rio. Canadian Journal of Forest Research, 22, 776-784. diction (419-427). Minneapolis, USA: North Central
Gualdi, V. (1979). The productivity of even-aged stands of Pinus Forest Experimental Station, U.S. Department of Agricul-
halepensis on the high plateau of Constantine in Algeria. ture, Forest Service.
Italia Forestale e Montana, 34(3), 101-120. Montero, G., Caellas, I. and Ruiz-Peinado, R. (2001). Growth
Herranz, J. M. (2000). Aspectos botnicos y ecolgicos del pino and yield models for Pinus halepensis Mill. Investigacin
carrasco (Pinus halepensis Mill.). Cuadernos de la Socie- Agraria: Sistemas y Recursos Forestales, 10(1), 180-201.
dad Espaola de Ciencias Forestales, 10, 13-17. Montero, G., Grau, J. M., Ruiz-Peinado, R., Ortega, C. and
Huang, S. (1999). Development of compatible height and site Caellas, I. (2000). Tablas de produccin para Pinus hale-
index models for young and mature stands within an pensis Mill. Cuadernos de la Sociedad Espaola de Cien-
ecosystem-based management framework. En: A. Amaro cias Forestales, 10, 183-188.
and M. Tom (Eds). Empirical and process-based models Newberry, J. D. (1991). A note on Carmeans estimate of height
for forest tree and stand growth simulation (61-98), Oei- from stem analysis data. Forest Science, 37(1), 368-369.
ras, Portugal: Edioes Salamandra. Novak, K., Luis, M., ufarc, K. and Ravents, J. (2011). Fre-
Kiviste, A. K., lvarez-Gonzlez, J. G., Rojo-Alboreca, A. and quency and variability of missing tree rings along the
Ruiz-Gonzlez, A. D. (2002). Funciones de crecimiento stems of Pinus halepensis and Pinus pinea from a semia-
de aplicacin en el mbito forestal. Monografas INIA: rid site in SE Spain. Journal of Arid Environments, 75(5),
Serie Forestal n 4. Madrid, Espaa: Instituto Nacional 494-498.
de Investigacin y Tecnologa Agraria y Alimentaria Palah, M., Tom, M., Pukkala, T., Trasobares, A. and Montero,
(INIA). G. (2003). Site index model for Pinus sylvestris in north-
Lopez-Senespleda, E., Bravo-Oviedo, A., Alonso, R. and Mon- east Spain. Forest Ecology and Management, 187, 35-47.
tero, G. (2014). Resource Communication. Modeling Panetsos, K. P. (1981). Monograph of Pinus halepensis (Mill.)
dominant height growth including site attributes in the and P. brutia (Ten.). Analiza Sumarstvo, 9(2), 39-77.

158
Madera y Bosques vol. 23, nm. 1: 143-159 Primavera 2017

Pard, J. (1957). La Productivit des Forts de Pin dAlep en Espaa: Instituto Nacional de Investigacin y Tecnologa
France. Annals de lEcole National des Eaux et Forts, Agraria y Alimentaria.
15(2), 365-414. Sharma, M., Amateis, R. L. and Burkhart, H. E. (2002). Top
Parresol, B. R. and Vissage, J. S. (1998). White pine site index height definition and its effect on site index determination
for the southern forest survey. (Res. Pap. SRS-10). Ashe- in thinned and unthinned loblolly pine plantations. Forest
ville, USA: Southern Research Station, Department of Ecology and Management, 168, 163-175.
Agriculture, Forest Service. Sloboda, V. B. (1971). Zur Darstellung von Wachstumprozes-
Pita, P. A. (1964). La calidad de la estacin en las masas de sen mit Hilfe von Differentialgleichungen erster Ordung.
Pinus sylvestris de la Pennsula Ibrica. Anales del Insti- Freiburg, Germany: Mitteillungen der Badenwrttem-
tuto Forestal de Investigaciones y Experiencias, 9, 5-28. bergischen Forstlichen Versuchs und Forschungsanstalt.
Pita, P. A. (1965). Crecimiento y produccin de las masas fores- Souleres, G. (1975). Site-quality classes and yield of Tunisian
tales espaolas (Resumen de la medicin de parcelas en el Pinus halepensis forests. Revue Forestiere Francaise,
ao 1965). Anales del Instituto Forestal de Investigacio- 27(1), 41-49.
nes y Experiencias, 10, 35-59. Tahar, S., Palahi, M., Garchi, S., Bonet, J. A., Ammari, Y. and
Pita, P. A. (1966). Clasificacin provisional de las calidades de Pique, M. (2012). Modeling dominant height growth in
estacin en las masas de pino pionero. Anales del Insti- planted Pinus pinea stands in Northwest of Tunisia.
tuto Forestal de Investigaciones y Experiencias, Tomo II, International Journal of Forestry Research, Article ID
171-182. 902381. doi: 10.1155/2012/902381
Pita, P. A. (1991). Potencialidad de las estaciones forestales. Tom, M., Ribeiro, F. and Soares, P. (2001). O modelo Globu-
Curvas de calidad. En: Seminario sobre Inventario y lus 2.1 (Relatrios Tcnico-cientficos do GIMREF n 1).
Ordenacin de Montes (Unidad Temtica 1, 18-39). Val- Lisboa, Portugal: Universidad Tcnica de Lisboa-ISA.
san, Espaa: Tragsa. Vargas-Larreta, B., Aguirre-Caldern, O. A., Corral-Rivas, J.
Ramrez-Maldonado, H., Bailey, R. L. and Borders, B. E. J., Crecente-Campo, F. and Diguez-Aranda, U. (2013). A
(1988). Some implications of the algebraic difference dominant height growth and site index model for Pinus
approach for developing growth models. In A. R. Ek, S. pseudostrobus Lindl. in northeastern Mexico. Agrocien-
R. Shifley and T. E. Burk (Eds.). Proceedings IUFRO con- cia, 47, 91-106.
ference on forest growth modelling and prediction (731- Vennetier, M. and Herve, J. C. (1999). Short and long term evo-
738). Minneapolis, USA: Department of Agriculture, lution of Pinus halepensis (Mill.) height growth in Pro-
Forest Service. vence (France) and its consequences for timber production.
Richards, F. J. (1959). A flexible growth function for empirical In T. Karjalainen, H. Spiecker and O. Laroussinie (Eds.).
use. Journal of Experimental Botany, 10, 290-300. EFI Proceedings, 27 International Seminar Causes and
Rhle, H. (1992). Ertragstafel fr die Aleppokiefer (Pinus hale- consequences of accelerating tree growth in Europe (pp.
pensis) in Israel. Munich, Germany: Lehrstul fr Wald- 253-265). Nancy, France: EFI & Ecofor.
wachstum-kunde der Universitt Mnchen.
SAS/STATTM Users Guide (Relase 8.2.) [Software] (2001).
Cary, USA: SAS Institute Inc.,
Received: 12 may 2016.
Schumacher, F. X. (1939). A new growth curve and its applica- Accepted: 3 february 2017.
tion to timber yield studies. Journal of Forestry, 37, 819-
This paper must be cited as:
820. Rojo-Alboreca, A., Cabanillas-Saldaa, A. M., Barrio-Anta, M., Noti-
vol-Pano, E. and Gorgoso-Varela, J. J. (2017). Site index curves for
Serrada, R., Montero, G. and Reque, J. A. (Eds.) (2008). Com-
natural Aleppo pine forests in the central Ebro valley (Spain). Madera
pendio de selvicultura aplicada en Espaa. Madrid, y Bosques, 23(1), 143-159. doi:10.21829/myb.2017.231495

159

Potrebbero piacerti anche