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Brazilian Journal of Biology

Print version ISSN 1519-6984On-line version ISSN 1678-4375

Braz. J. Biol. vol.64 no.2 São Carlos May 2004

https://doi.org/10.1590/S1519-69842004000200009 

Behaviour of dispersion indices in pattern detection of a population of angico, Anadenanthera peregrina (Leguminosae)

 

Padrão de agregação do angico Anadenanthera peregrina

 

 

Malhado, A. C. M.; Petrere Jr., M.

Departamento de Ecologia, UNESP, C.P. 199, CEP 13506-900, Rio Claro, SP, Brazil

Correspondence

 

 


ABSTRACT

In this paper we calculate the values of eight pattern detection indices, using different quadrat sizes where individuals of angico above 1.5 m were located, in order to examine their statistical behaviour with increasing sample size. It was concluded that the best index is the standardized Morisita index (Ip) which is completely independent of sample size.

Key words: spatial pattern, aggregation, angico, Anadenanthera peregrina.


RESUMO

Neste trabalho calculamos os valores de oito índices de detecção de padrões, usando quadratins de tamanhos diferentes, onde indivíduos de angico com mais de 1,5 m estavam localizados, a fim de examinar seus comportamentos estatísticos com o aumento do tamanho da amostra. Conclui-se que o melhor índice é de Morisita padronizado (Ip), o qual é independente do tamanho da amostra.

Palavras-chave: padrão espacial, agregação, angico, Anadenanthera peregrina.


 

 

INTRODUCTION

In ecological or population studies, the pattern is defined by Ludwig (1979 circa Rossi & Higuchi, 1998) as a quantitative description of the horizontal distribution of individuals of a species within a community. This has been widely studied by comparing communities and ecosystems, as a means of providing a mechanism to foresee the functional state of the system.

The pattern of plants and animals is a fundamental characteristic of a population. The patterns exhibited by a population living in a given geographic area can be of three basic types: random, clumped, or uniform (Pielou, 1977; Southwood, 1978; Elliot, 1979; Matteucci & Colma, 1982; Odum, 1986; Krebs, 1989, 1999; Carvalho, 1992; Buschini, 1999; Petrere, 1985).

According to Pielou (1977), Odum (1986), and Krebs (1999), the clumped type is the most commonly observed pattern. The main reasons that can lead to a clumped pattern in a population are the characteristics of the species, the relationship between them, and with the environmentally variations (Kershaw, 1973; Matteucci & Colma, 1982; Meirelles & Barreto Luiz, 1995; Soviano, 1997). Krebs (1999) pointed out that the most important part of the pattern is the ecology behind it, i.e., the causal mechanisms and the factors that promote and maintain it.

Since the individuals within a population tend to form groups of different sizes and also because the tendency for randomness likely varies for members of a given group, there are several degrees of clumping that can be described (Elliot, 1979; Vandermeer, 1981; Odum, 1986; Krebs, 1989; Carvalho, 1992).

Meirelles & Barreto Luiz (1995), working with 18 tree species in the cerrado (savannah-like vegetation) of the Experimental Ecological Farm of the University of Brasília, obtained 16 species with a clumped pattern and only two populations with a random pattern. This result corroborates the suggestion that the clumped pattern is most often observed. However, the work of Rossi & Higuchi (1998) failed to support this theory; these authors observed that, within a total of 8 species studied in the Amazonian Rain Forest, two species showed a clumped pattern, while the others showed a predominantly random pattern.

Among the applications of pattern analysis stand its use in forestry surveys, which sets the base for gathering information for forest management. Also worth mentioning is its application in management systems based on natural regeneration, in planning mechanized exploitation, and in implementation forestry methods, as well as in defining the size of an area selected for conservation purposes (Rossi & Higuchi, 1998). Krebs (1999) further noted that pattern analysis could also allow the exact choice of methods to estimate population density. This point was also made by Odum (1986), who stated that pattern analysis is important for selection of sampling procedures for ecological studies.

Nowadays, there is a proliferation of quantitative tools and acceptance about their use in formulating and solving ecological problems. Within this context, the aim of the present work is to observe the behaviour of statistical indices for the pattern detection of a tree species, the angico Anadenanthera peregrina, in a population from Rio Claro (SP).

 

MATERIAL AND METHODS

This study was carried out in a secondary forest located in the Horto Municipal Navarro de Andrade, Municipality of Rio Claro, São Paulo State, Brazil. The study species, Anadenanthera peregrina, commonly known as angico, angico-vermelho, angico-do-morro, angico branco, paricá, ricá-de-curtume, and paricá de terra-firme, is a pioneer species of the family Leguminosae (Lorenzi, 1998). This species has a wide geographical distribution, occurring in semideciduous forests and in the transition to cerrado vegetation, in the states of Tocantins, Goiás, Bahia, Minas Gerais, Rio de Janeiro, São Paulo, Mato Grosso, and Mato Grosso do Sul (Lorenzi, 1998).

Albeit frequently used and cited, the sampling method used here has the disadvantage inconvenien of using arbitrary sampling units. It is worth noting that different quadrat sizes should be considered when using this method. In the case of a species with a clumped pattern for example, the quadrat size that will detect it is affected by the size of the group of individuals. Thus, it is imperative to use different quadrat sizes to detect clumped patterns (Kershaw, 1973); Matteucci & Colmas, 1982; Meirelles & Barreto Luiz, 1995; Krebs, 1999).

Initially we determined, in an area of 9600 m2 (120 m x 80 m), all the spatial coordinates (x,y) of individuals of Anadenanthera peregrina higher than 1.5 m. Measurements were carried out with the aid of a tape placed on the lateral boundaries of the study area.

Quadrats of different sizes (1 x 1 m, 2 x 2 m, 4 x 4 m, 5 x 5 m, 10 x 10 m, 20 x 20 m, and 40 x 40 m) were considered in order to evaluate the effects of the size by analyzing the pattern variations among them. Afterwards, dispersion indices were used to observe valve behaviour with respect to the pattern diagnosis.

The indices used were: the variance-to-mean ratio (I), Morisita's dispersion index (d), standardized Morista index (Ip), 1/k index (inverse of the negative binomial parameter), and four other indices based on the variance-to-mean ratio: David & Moore index, Lexis index, the coefficient of Charlier, and the coefficient of Green.

All the formulas, calculations, and statistical tests of goodness of fit were based on Krebs (1989, 1999) and Elliot (1979).

 

RESULTS

The fieldwork listed 227 individuals of Anadenanthera peregrina higher than 1.5 meters.

Although not shown here, (Malhado, 2000) the indices variance-to-mean ratio (I), Morisita (d), and standardized Morista (Ip) detected, within their limits of significance for the X2 test, values that corresponded to a clumped pattern for the angico population in all quadrat sizes. It was also observed (Malhado, 2000) that the calculated values in the k index, its inverse, David & Moore index, Lexis index, the Charlier coefficient, and the Green coefficient, as well the values for the maximum uniform, clumped, and random patterns, were located between the maximum expected values for these patterns, with a tendency to closely approximating randomness.

The behaviour of the values found for each of the dispersion indices, as well as for deviations from the random pattern, can be seen in Figs. 1-8. The curves for the indices of the variance-to-mean ratio (Fig. 1), the David & Moore index (Fig. 5), and that of Lewis (Fig. 6) increased with quadrat size increase, indicating a tendency for higher levels of clumping, since the values were different from those expected for randomness. On the other hand, the indices of Morisita (Fig. 2), 1/k (Fig. 4), and the Charlier coefficient (Fig. 7) showed descendent curves, following the same tendency towards an increase in the quadrat size. The only curve that did not demonstrate marked differences in behaviour was the standardized Morisita (Fig. 3) which showed a curve paralleling the curve describing the random pattern, suggesting independence of quadrat size. The Green coefficient (Fig. 8) started to increase slightly after the 20 x 20 m quadrat.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

DISCUSSION

The present work corroborated Pielou (1977), Odum (1986), and Krebs (1999) who observed that the clumped pattern is the most often detected in natural populations; in this work, such a pattern was observed by analyzing the indices of the variance-to-mean ratio, the Morisita, and standardized Morisita, all of them with good fit.

The 1/k, David & Moore, and Lexis indices, and the coefficients of Green and Charlier do not have known variance, which precludes calculating their significance limits. This fact hampered the use of statistical tests to detect random patterns, thus restricting their utility for pattern determination anchored in hypothesis tests. Probably, this disadvantage is responsible for the low use of these indices for pattern detecting. Krebs (1999) stated that the Green index is the best, as it is independent of population density and sample size, although evidence was shown here of a slight increase with quadrat size. The great disadvantage it presents is that its exact variance is unknown.

Although we cannot test the significance of the values of the David & Moore, Lexis, 1/k, Charlier and Green indices, they all showed a tendency towards randomness for our data.

The indices based on the variance-to-mean ratio have the drawback of being strongly dependent on the sampling unit size (Rossi & Higuchi, 1998); the previously cited authors also emphasize that this criticism can be applied to the majority of indices that are obtained based on sampling units with a defined area. This property become advantageous, however, if the objective is to observe enhancement of the different scales at which a given pattern can occur. In our work, indices derived from the variance-to-mean ratio enhanced the level of clumping angico population.

Among all the indices for pattern detection currently available, the most often used, is the Morisita index (d) to judge by the work of Oliveira et al. (1989), Meirelles & Barreto Luiz (1995), Bergamin (1998), Leitão (1998), And Rossi & Higuci (1998). Rossi & Higuchi (1998) stated that the main reason for its use is that this index is less affected by the sampling unit size. These authors further suggested that the most adequate indices for pattern analysis are the Morisita (d) and the variance-to-mean ratio; Myers (1978) shared the same opinion about the last index.

The behaviour of the indices as a function of quadrat size variation allowed the description of three different curves (increasing, decreasing, and parallel), which endorsed the variety of mathematical calculations seeking to delineate a given pattern. PIELOU (1977) further stressed that each index is only a simple statistical analysis and, thus, can only describe a simple aspect of another complex pattern.

The identified parallel curve behaviour of the standardized Morisita index, and to a lesser degree the coefficient of Green, confirmed the assertions of Myers (1978) and Krebs (1999) that these indices are independent of population density and sample size.

The graphics for the values observed for the variance-to-mean ratio (Fig. 1) and Morisita (Id-Fig. 2), as a function of the difference in quadrat sizes, are similar to those found by Oliveira et al. (1989) on a logarithmic scale; in this case, the curve for the variance-to-mean ratio has an ascendant behaviour while the curve for the Morisita index has a descendent one. Meirelles & Barreto Luiz (1995) in their studies on different quadrat sizes also obtained differences in pattern detection values when using these two indices. In the work of these authors, we observed the same pattern described for the species Ouratea hexasperma, Qualea grandiflora, and Sclerobium aureum, the only one that showed calculated values statistically higher than 1 (clumped pattern). We noted in the study of Rossi & Higuchi (1998) the same pattern for both indices in the species Micrandropsis scleroxylon. It is worth noting that this species is singular in that it showed a clumped pattern irrespective of quadrat size, a fact which we related to through the replication of the behaviours previously described the detection of a clumped pattern.

It is important to point out that these indices have limitations and criticism exist as to their use, which can be observed in the simulation works of Myers (1978), Hurlbert (1990), and Perry (1995).

Finally, we must emphasize that our results can hardly be generalized to a wider geographical area, as the data are based on a secondary forest where succession took place in a particular site.

Acknowledgments — We thank Dra. Leila Cunha, from the Department of Ecology of UNESP, for her criticisms; and FAPESP, for a Scientific Initiation Scholarship ACMM (Processo IC 00/00505-5); and UNESP and CNPq for financial support.

 

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Correspondence to
Miguel Petrere Júnior
Departamento de Ecologia, UNESP, C.P. 199
CEP 13506-900, Rio Claro, SP, Brazil
e-mail: mpetrere@rc.unesp.br

Received August 27, 2002 - Accepted February 17, 2003 - Distributed May 31, 2004

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