SciELO - Scientific Electronic Library Online

vol.35 issue5Regeneration in a natural population of Araucaria angustifolia (Araucariaceae)Evaluation of ecological preferences of Clidemia urceolata DC. on disturbed ecosystems author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand




Related links


Revista Árvore

Print version ISSN 0100-6762

Rev. Árvore vol.35 no.5 Viçosa Sept./Oct. 2011 

Edge effect on tree diversity, composition and structure in a deciduous dry forest in Central Brazil


Efeito de borda na diversidade, composição e estrutura da comunidade arbórea em uma floresta estacional decidual no Brasil Central



Alexandre Bonesso SampaioI; Aldicir ScariotII

IInstituto Chico Mendes de Conservação da Biodiversidade, ICMBio, Brasil, E-mail:
IIEmbrapa Recursos Genéticos e Biotecnologia, EMBRAPA/CENARGEN, Brasil, E-mail:




The effects of edge distance on the structure, composition and diversity of tree community, considering individuals of all size classes, were studied in a well-preserved fragment of deciduous dry forest in northeastern Goiás state, Brazil. Plots were systematically established at six distances (0, 40, 80, 160, 280 and 400 m) from the edge, over 10 orthogonal transects on the forest-pasture edge. It was sampled 602 adult individuals/ha, 8,927 saplings/ha and 54,167 seedlings/ha distributed in 58 species. Although the composition of seedlings and adult individuals varied significantly over the forest-pasture gradient, the variation explained by edge distance was below 4%. Among parameters of community structure and tested diversity indexes, there was significant variation only for diversity of seedlings and height of adult trees among forest-pasture edge distances. The dry forest fragment showed only a slight edge effect on the evaluated tree community parameters. This conclusion contrasts with findings from studies on tropical rain forests which indicate sharp differences between edge and interior tree communities in forest fragments.

Keywords: Biodiversity conservation, Forest fragmentation and Seasonal forest.


O efeito da distância da borda na estrutura, composição e diversidade da comunidade de árvores, considerando todos os tamanhos de indivíduos, foi estudado em um fragmento bem preservado de Floresta Estacional Decidual no Nordeste do Estado de Goiás, Brasil. Parcelas foram sistematicamente estabelecidas em seis distâncias (0, 40, 80, 160, 280 e 400 m) da borda, ao longo de 10 transecções ortogonais na borda floresta-pastagem. Foram amostrados 602 indivíduos adultos/ha, 8.927 indivíduos juvenis/ha e 54.167 plântulas/ha distribuídas em 58 espécies. Embora a composição de plântulas e adultos tenha variado significativamente ao longo do gradiente floresta-pastagem, a variação explicada pela distância da borda foi abaixo de 4%. Entre as variáveis de estrutura da comunidade e os índices de diversidade testados houve variação significativa apenas na diversidade de plântulas e na altura de adultos entre as distâncias da borda floresta-pastagem. O fragmento de floresta estacional apresentou apenas tênue efeito de borda, considerando-se os parâmetros de comunidade avaliados. Essa conclusão contrasta com resultados encontrados em florestas tropicais úmidas, os quais indicam diferenças abruptas entre a comunidade de árvores da borda e as do interior de fragmentos florestais.

Palavras-chave: Cerrado, Conservação da biodiversidade e Fragmentação de florestas.




Forest fragmentation reduces natural habitats and creates an edge between the original vegetation and the new human-disturbed area (LAURANCE; BIERREGAARD, 1997). Edges change abiotic conditions, which may affect the abundance and distribution of organisms in the remaining native habitat (LAURANCE; BIERREGAARD, 1997; BENITEZ-MALVIDO, 1998; SCARIOT, 1999), even in large fragments (LAURANCE, 2000). Edge effects may restrict the distribution of many organisms to the interior of forest fragments (MURCIA, 1995), and consequently the effective area conserved can be smaller than the present reserve area.

Microclimatic and edaphic conditions at forest edge are generally different from fragment interior (KAPOS, 1989; CAMARGO; KAPOS, 1995; JOSE et al., 1996; WILLIAMS-LINERA, et al., 1998; BURKE; NOL, 1998; RODRIGUES, 1998; DIDHAM and LAWTON, 1999; DAVIES-COLLEY et al., 2000; GEHLHAUSEN et al., 2000; DELGADO et al., 2007, POHLMAN, 2009). These studies indicate that edges have higher values of air and soil temperature, wind speed, vapor pressure deficit, and lower air and soil humidity than forest interior. These altered microclimate conditions affect plant physiology (KAPOS et al., 1993; HERBST et al., 2007), possibly increasing tree mortality (ESSEEN, 1994, D'ANGELO et al., 2004) and causing changes in diversity, composition, structure and dynamics of plant communities at edges of forest fragments.

The processes that rule edge effects in forest fragments are well understood and reasonably consistent throughout the studies carried out in temperate (WHITNEY; RUNKLE, 1981; PALIK; MURPHY, 1990; MATLACK, 1994; HANSSON, 2000) and tropical rain forests (LOVEJOY et al., 1983; WILSON; CROME, 1989; WILLIAMS-LINERA, 1990a; LAURANCE, 1991; LAURANCE et al., 1998; RODRIGUES, 1998; WILLIAMS-LINERA et al., 1998; LAURANCE et al., 2006). However, edge effect trends found elsewhere may not be directly applicable to tropical dry forests.

Tropical dry forests, the most endangered and probably the most fragmented lowland forest in the tropics (JANZEN, 1988; LERDAU et al., 1991; WHITMORE, 1997), have relatively low species diversity (GENTRY, 1995), but have a large life form diversity, which is attributed to the high temporal and spatial heterogeneity in water availability that characterizes these forests (MEDINA, 1995). Similarly to what happens to species diversity, biomass accumulation in dry forests is also limited by water shortage, thus these communities have lower average basal area, height (HOLBROOK et al., 1995) and lower tree density than rain forests (GILLESPIE et al., 2000). Dry tropical forests canopies are more open than the canopy of rain forests and leaf shedding during the dry season increases canopy opening even more (VIEIRA; SCARIOT, 2006). Consequently, it is expected a less contrasting forest-edge microclimate gradient in dry forests than in rain forests, affecting organisms to a smaller extent. Another aspect is that among the reduced species pool in dry forest, it might be less likely to find species that are affected by fragmentation consequences (LAWES et al., 2005). Due to differences in the forest structure (tree height, basal area, density), richness and seasonality (deciduousness) between rain and dry forests, it is anticipated that tropical dry forests may respond differently from rain forests to edge effects.

It was studied the edge effects on the tree community of a deciduous dry forest in Paranã River Valley, central Brazil, to assess whether there are edge effects on structure (basal area, height, diameter and density), species composition and diversity. The findings of this study may contribute to the design and management of reserves in this region and other similar dry forest areas.



2.1. Study area

This study was conducted in a deciduous dry forest in the municipality of São Domingos, in northeastern Goiás State (Figure 1). The forest is located on the Paranã River Basin, a tributary of the Tocantins River.

The climate in the Paranã River Basin is tropical (Aw) with two well-defined seasons. Annual mean temperature is 23ºC. The highest temperatures occur in September-October, and in the coldest month, temperatures are above 18ºC. Mean annual precipitation is 1300-1500mm, 70% of which falls between October and April, whereas dry conditions during three to four of the remaining months result in water deficit (IBGE, 1995).

The Paranã River Basin is characterized by different kinds of vegetation patchily distributed in the landscape, such as deciduous dry forests on flat terrains, deciduous dry forests on limestone outcrops and on slopes, open savanna (cerrado) and woodland savanna (cerradão) physiognomies, and riparian forests along the rivers. The vegetation distribution might be determined by soil characteristics and deciduous forests tend to occur on the richer soils, usually Alfisols with high Ca and Mg levels (SCARIOT; SEVILHA, 2000).

The 59,404 square kilometers of the Paranã River Basin was originally covered by forests, savannas or limestone rock outcrops, but today the landscape matrix is dominated by cattle ranches. From 1988 to 1993, over 21% of the original vegetation cover was removed (LUÍZ, 1998). Even more recently, the deforestation has not stopped. Considering a sample area of 181,000 ha of the Paranã River Basin, 67% of the forest cover remaining in 1991 was deforested until 1999 (ANDAHUR, 2001). The remaining forest fragments are used as refuges and foraging sites for cattle and economic valuable timber species are extracted by ranch owners.

The forest fragment studied in this work covered 900 ha. This area can be divided according to vegetation type and human disturbance (Figure 1). It was sampled only a homogeneous portion of the fragment (13039'26''S, 46045'09''W) characterized by deciduous dry forest that showed no signs of timber exploitation and cattle foraging was the only noticeable human impact. The sampled area abutted disturbed seasonal dry forest and pasture and it was close to a woodland savanna (cerradão) patch. The studied forest fragment was located on a flat terrain (<3% inclination) more than 1.5km away from any water course, on Alfisol soil (pH in water = 6.6 ± 0.5, Ca = 9.0 ± 4.2 meq/100g, Mg = 1.7 ± 1.0 meq/100g, average and standard deviation of 83 soil samples taken in the studied fragment and other forests of the same type in the region).

The pasture adjoining the studied forest edge was established about 30 years ago and the original vegetation in the pasture area was seasonal deciduous forest according to satellite images, information from the landowner, remnant tall trees and resprout (VIEIRA et al., 2006). The pasture was planted with Braquiaria decumbens Stapf forage grass species and is annually tractor mowed to prevent the grass suppression by the natural regeneration, which is the regular pasture management system in the region (SAMPAIO et al., 2007).

Edge effect may vary depending on several characteristics such as fragment age, size, shape, management of the surrounding matrix and edge aspect (MURCIA, 1995). In the Paranã River Basin, it is impossible to find true replicates for forest-pasture edge with the same age, vegetation type, facing the same direction, with the same conservation and/or management history. It is especially true because the original vegetation was patchily distributed and the management history was highly variable in this region. Since it was unfeasible to account for all landscape heterogeneity the sampling effort was focused to test in detail the edge effect in only one forest fragment, characterizing pseudo-replication (HURLBERT, 1984).

2.2. Sampling

Along the forest-pasture NE edge, 10 400-m perpendicular transects were systematically established, 100 m apart from each other (Figure 1). Along each transect, it was established 20 × 20 m plots at six distances (0, 40, 80, 160, 280 and 400 m, totaling 60 plots with an aggregate area of 2.4 ha) where all adult trees (dbh - diameter at breast height > 5 cm) were sampled. Within each plot, in the lower right corner, it was delimited a 5 × 5 m subplot to sample saplings (dbh < 5 cm and height > 1m) and a 2 × 2 m subplot to sample seedlings (height < 1 m, Figure 1). Height and diameter were recorded for all adults (dbh), saplings (diameter at 30 cm above soil), and seedlings (diameter at 2 cm above soil) individuals. Sampling was conducted from March to May 2000, at the end of the rainy season. Botanical vouchers were collected, species identifications were made by comparison to herbaria specimens and deposited at the Cenargen-Embrapa Herbarium (CEN) in Brasília, Brazil.

2.3. Data analysis

Species richness (S), Shannon-Weiner diversity (H') and Pielou's equitability (J') were estimated for the three size classes in each plot, based on natural logarithms (MARGURRAN, 1988).

Estimates of S, H', J', mean height, diameter and plant density were individually compared by using MANOVA for repeated measures, using the Statistica software package (STATSOFT, INC., 2000). The MANOVA for repeated measures was used as a way to take into account the non-independence among samples (TABACHNICK; FIDELL, 1989; VON ENDE, 1993). In this case, distances to forest-pasture edge was modeled as repeated measures. To assess significance, it was used Pillai's statistics, which are more robust for data that do not completely satisfy the multivariate analysis assumptions (TABACHNICK; FIDELL, 1989).

To compare species composition at each edge distance, mean dissimilarity curves were used for each size class. These curves were estimated by progressively taking sub-samples of increasing size of the total sample (10 plots) for each treatment (distance from the edge). For each sub-sample size (area) the mean dissimilarity was estimated (1 - Sørensen index) using PC-ORD (MCCUNE; MEFFORD, 1997). Pairs of curves were compared for each size classes with Kolmogorov-Smirnov tests (ZAR, 1999).

Proportional similarity index (PS) was used between edge distances for each size class (BROWER et al., 1990) to estimate species composition similarity. To identify changes in species composition and their relationship with edge distance (TER BRAAK, 1987), it was performed a direct gradient analysis through a Canonical Correspondence Analysis (CCA). Significant correlations among plots were estimated with a Monte Carlo test (TER BRAAK, 1987). For these analyses two matrices were used, one of abundance of individual species in the 60 plots and other of plot distances to the nearest forest-pasture edge, treated as an indicator of environmental gradient.



A total of the 4,083 individuals from 58 species and 20 plant families were sampled. Leguminosae was the richest family with 21 species. From this total, 1,444 (602/ha) were adult trees from 54 species, 1,339 (8,927/ha) saplings distributed in 47 species and 1,300 (54,167/ha) seedlings belonging to 42 species (Table 1).

3. 1. Diversity

For all size classes, species richness did not change significantly with edge distance (Pillai's = 0.37-0.55, F = 0.59-1.23, P = 0.41-0.71, df = 5, 5, Table 2). The Shannon-Weiner (H') diversity index for adults and saplings individuals was also not significantly affected by edge distance (Pillai's = 0.33, 0.67, F = 0.49, 2.03, P = 0.23, 0.77, respectively, df = 5, 5, Table 2). In contrast, there was an increasing trend of seedlings diversity from edge to forest interior (Pillai's = 0.90, F = 8.92, P = 0.016, df = 5, 5, Figure 2 - A), but Post hoc multiple comparisons did not indicate significant differences among distances.

Equitability (J') did not change with edge distance for any size classes (Pillai's = 0.46-0.63, F = 0.86-1.73, P = 0.28-0.565, df = 5, 5, Table 2). Likewise, species dissimilarity curves did not differ among edge distances for any size class (Kolmogorov-Smirnov test, seedling: P = 0.31-1.0, sapling: P = 0.66-1.0, adults: P = 0.96-1.0).

3.2. Composition

The vast majority (35 species) of the sampled species was found in all distances to forest-pasture edge (Table 1). The most abundant species for all size classes were found in all distances, only the less abundant species were restricted to certain edge distances.

Based on similarity index, there is no evident trend on species composition related to edge distance for all tree size classes. Similarity was always higher than 50% for saplings and adults. For seedlings, similarity among plots was lower than 50% for nearly half of the compared distance pairs. In general there was more variation in percentage similarity (PS) among edge distances for seedlings (range: 36-65%) than for saplings (60-81%) and adult trees (62-77%). For seedlings, the lowest similarity was between the plots closest to the edge (0 and 40 m), and the highest similarity between the most interior plots (280 and 400 m). Saplings showed a different trend, with the highest similarity between plots closest to the edge (0 and 40 m), and the lowest similarity between the most distant plots (0 and 400 m). Adult trees did not follow any pattern. Species in adult size class were more evenly distributed along the edge-interior gradient of the forest, with 20 (37%) species occurring at all distances compared to 12 (25.5%) at saplings and 10 (23.8%) at seedlings size classes.

According to the Canonical Correspondence Analysis (CCA), tree species composition of the studied forest fragment was significantly related to the distance to forest-pasture edge for seedlings (F = 1.48, P = 0.037, df = 1, 57, n = 60, 1,000 permutations, Figure 3) and adults (F=2.1583, P = 0.001, df = 1, 58, n = 60, 1000 permutations, Figure 3). However, only a very small fraction of the variation within the first CCA axis, in both size classes, was explained by the edge distance (2.5% for seedlings, CCA1-eigenvalue = 0.06, and 3.6% for adults, CCA1-eigenvalue = 0.06). In fact, for seedlings, the CCA was only significant after excluding an outlier plot that contained an abnormally high (>100 times higher) abundance of Schinopsis brasiliensis, all concentrated under the mother tree abutting to this plot. For adults, all the plots with more than two units of variation in the first CCA axis are only separated from the others due to a higher abundance of a single species, Combretum duarteanum, in these plots. For both seedlings and adults, the majority of plots across distances are grouped together and enclosed in between one unit of variation around zero in the first CCA axis (Figure3). The most distinct plots for both seedlings and adult communities are mainly in the extremes of the edge distance gradient (0 and 400 meters). Finally, for saplings, species composition was unrelated to edge distance (F = 1.39, P = 0.068, df = 1, 58, n = 60, 1,000 permutations).

3.3. Structure

Despite the lower number of seedlings and adult individuals in plots located closest to the edge (0 m plots), mean density did not significantly change with edge distance for any size classes (Pillai's = 0.37-0.61, F = 0.57-1.54, P = 0.32-0.72, df = 5, 5, n = 10, Table 2). For all size classes there were no significant changes (Table 2) in mean diameter (Pillai's = 0.22-0.63, F = 0.28-1.68, P = 0.29-0.91, df = 5, 5, n = 10) and basal area with edge distance (Pillai's = 0.33-0.67, F = 0.49-2.03, P = 0.23-0.77, df = 5, 5, n = 10).

Mean height of seedlings and saplings individuals did not change with edge distance (Pillai's = 0.28-0.64, F = 0.38-1.81, P = 0.26-0.84, df = 5, 5, n = 10). Although adult tree height varied (Pillai's = 0.90, F = 8.80, P = 0.01, df = 5, 5, n = 10) (Table 2, Figure 2 - B) with the plots closest to the edge (0 m) showing lower mean height than the plots at 40 meters (Bonferroni Post hoc test, P = 0.032).



The assumptions made based on results from this work must be carefully considered because only one forest-pasture edge was sampled. Edge effect may vary depending on several factors such as fragment age, size, shape, matrix management and edge orientation which were not considered by the present study (MURCIA, 1995). Nonetheless, the studied fragment has structure and species composition similar to other seasonal deciduous forests in the region (SCARIOT; SEVILHA, 2000), indicating that the inconspicuous edge effect found in the studied area might occur in other areas with the same vegetation type in the Paranã River Valley, Central Brazil.

The absence of edge effect in forest fragments has been found in recent studies. Even in the Amazon rain forest, where edge effects were considered formerly as one of the most extensive impacts for biodiversity conservation of forest fragments (LAURANCE, 2000; LAURANCE et al., 2006). PHILLIPS et al. (2006) reported the absence of edge effects fragments in rain forests from the Southwestern Peruvian Amazon. Another example shows that neither richness nor abundance of woody seedlings was affected by edge effect in Afromontane forests in South Africa (LAWES et al., 2005). Absence of edge effects was also found in a temperate forest, where tree growth is more related to soil and topography characteristics than to edge effect (MCDONALD; URBAN, 2004).

In this work, diversity of tree species in adult and sapling size classes was not affected by edge effect. This result contradicts most studies in tropical and temperate forests on edge effects that found less species in edges compared to forest interior (BURKE; NOL, 1998; RODRIGUES, 1998; GOLDBLUM; BEATTY, 1999; GEHLHAUSEN et al., 2000; OLIVEIRA FILHO et al., 2004). The only noticeable edge effect in the studied forest fragment in terms of species diversity was found in the seedlings class. This effect was a slight reduction on seedlings diversity with the edge proximity. Seedling can be the first size class to be affected by edge effect, because they are the life stage more sensitive to the environment or biotic interactions (SAUNDERS et al., 1991; RODRIGUES, 1998). High predation or harsh environmental conditions in the edge may be restricting the recruitment of some species in detriment of others (HOLL; LULOW, 1997; WONG et al., 1998; SONG; HANNON, 1999; CADENASSO; PICKETT, 2000; NAVA-CRUZ, 2007). Nonetheless, community structure of seedlings is very dynamic, after the fruiting season that happens during the beginning of the rainy season in dry forest regions (VIEIRA; SCARIOT, 2006) the forest floor tends to be covered by seedlings. Then, by the end of the rainy season and beginning of the next dry season, most of those seedlings die (CABIN, 2002). Therefore, without following seedling dynamic is hard to make statements about edge effect on seedlings.

The species composition of trees in the adult and seedling size classes formed a gradient following the distance to forest-pasture edge, but there were no distinct communities occurring in forest interior or in edge habitat. A continuous variation in plant species composition associated with edge effect was also found in an Araucaria Forest in southern Brazil, possibly due to edge colonization by light demanding species (FONTOURA et al., 2006). Even though, in this study, the ordination axis for seedling and adult size classes were correlated to edge distance, this was a weak pattern because only a small part of the species composition variation was explained by the ordination axis. The lack of strong correlation of species composition with edge effect may not be an unusual pattern in Brazilian dry forests, Oliveira-Filho et al. (1997) reported an absence of edge effect in the species composition of adult trees found in a semi deciduous forest fragment in southeastern Brazil. Furthermore, in a tropical forest in Uganda, tree species composition did not vary with the edge-interior gradient, even though the analysis of each species separately showed significant correlations for most species with distance to forest-edge, considering one or more of the following parameters: density, relative abundance, relative frequency, relative dominance, importance value index and basal area (OLUPOT, 2009). Thus, edge effects may be impacting species individually in positive and negative manners which may be compensatory and prevent the detection of effects on the community level.

The only identifiable pattern of species composition in the studied fragment was a slightly distinct tree community in the transition of the deciduous dry forest and the woodland savanna patch (Figure 1). This pattern was found only for the individuals in the adult size class. The ordination analysis separated the plots in the dry forest-woodland savanna transition due to the much higher density of Combretum duarteanum. This pattern is probably not related to the forest-pasture edge effect because: (1) C. duarteanum populations are denser in the woodland savanna (A.B. Sampaio, personal observation) and (2) because other plots far from the savanna patch but at same forest-pasture edge distance were not grouped with the savanna-transition plots in the ordination analysis.

The mean height of trees in adult class was smaller in the edge compared to the interior plots. This pattern also found elsewhere might occur due to high mortality of tall trees in the edge during the first years after edge creation (ESSEEN, 1994; D'ANGELO et al., 2004). This may increase recruitment of new trees and subsequently reduce average tree height in the forest fragment edge. However, in the studied forest fragment this increased recruitment just after edge creation was probably not high enough to increase the density of trees. In other situations, this edge effect is more striking. CASENAVE et al. (1995) found both lower tree height and higher density at the edge in a semi-arid forest in the Argentinean Chaco and the same was reported in a temperate deciduous forest in Canada (BURKE; NOL, 1998). Also, Laurel and Pine forests in Tenerife, Canary Islands, had smaller trees in the edge compared to the forest interior (DELGADO et al., 2007).

Failure to detect evident edge effect on diversity and structure of tree community may result from several factors, such as: (1) Sampling scale - biotic changes might occur only within the first few meters from the edge, and not be detected due to larger scale plots (DIDHAM; LAWTON, 1999); (2) Edge dynamics as tree community parameters vary over time, edge effects might disappear over the years (MATLACK, 1994; WILLIAMS-LINERA et al., 1998; LAWES et al., 2005) or, alternatively, a few years or decades might not be not enough time for fragmentation effects to be noticeable (SCARIOT, 1999); (3) Edges interaction the effect of a single edge may not be strong enough to be detected but in small fragments where several edges interact, their combined effect may be significant (MALCOLM, 1994; DIDHAM; LAWTON, 1999); (4) Cattle browsing cattle foraging inside forest fragments may interact with edge effects confounding the results (PALIK; MURPHY, 1990).

Additionally, dry forests might actually be less vulnerable to edge effect than rain forests due to the fact that the species are more adapted to harsher environmental conditions and drought desiccation (VIEIRA; SCARIOT, 2006). In this context, edges become not as different from the forest interior as in tropical rain forests. One factor that might contribute to the resistance of dry forest species to disturbances, including edge effects, is the capacity of fast growth due to the nutrient rich soils where they usually occur (LAWES et al., 2005; VIEIRA; SCARIOT, 2006). The fast growth of tree species in Southwestern Amazon forests in rich soils was considered responsible for forest resistance to disturbance, such as gap creation, and explains the absence of edge effect in those forest fragments (PHILLIPS et al., 2006). Species-poor forests, such as dry forests (GENTRY, 1995), may have less chance to show edge effect on species richness (LAWES et al., 2005), i.e. less species or less rare species means lower risk to edge effects. Although the results from this work are in accordance with the hypothesis that edge effects are not so important in dry forests, this hypothesis which needs further specific studies to be confirmed was not tested in this work.



Most studies conducted in temperate and tropical rain forests detected evident edge effects (e.g. WILLIAMS-LINERA, 1990; LAURANCE et al., 1998; GEHLHAUSEN et al., 2000), although results do not elucidate a common pattern for all parameters studied (MURCIA, 1995) and there are even a few examples of less pronounced effects in these forests (MCDONALD; URBAN, 2004; LAWES et al., 2005; PHILLIPS et al. 2006). For dry forests, there are not enough studies on fragmentation to draw general conclusions about edge effect, but it is reasonable to expect differences to what was found so far for wetter forests. The present study contributes to the forest fragmentation knowledge by adding one more evidence to the fact that there are types of vegetation and conditions where edge effects may be negligible and that in these situations, management efforts should focus on restoration and deforestation reduction.



The authors of this work thank Jorge Meave, William Laurance, Isabel Schmidt, Maurício Sampaio and anonymous reviewers by relevant contributions to this article. Célia Cordeiro by helpful support in statistical analysis. Anderson C. Sevilha, Sálvio C. Xavier, Waldemar de S. Silva, Nilton F. Barbosa, many students and field assistants helped with fieldwork and Arlene Y. Goya with logistics. José Wagner B. Machado, Carolyn Proença, Ary T. Oliveira-Filho and Benedito A. da Silva helped to identify the plant species. José Pereira permitted us to work on his property. ABS had a fellowship from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior. This paper was part of the Master's thesis submitted to the Ecology Department of the University of Brasília and of the project "Strategies for the Conservation and Management of Semi Deciduous Forest Fragments" funded by Embrapa-Cenargen and Global Environmental Fund/World Bank/Programa Nacional da Biodiverside/Projeto de Conservação e Utilização Sustentável da Diversidade Biológica Brasileira/Ministério do Meio Ambiente/Conselho Nacional de Desenvolvimento Científico e Tecnológico.



ANDAHUR, J. P. V. Floresta e questões de gestão ambiental na bacia do vale do Paranã. 2001. Dissertação (Mestrado em Engenharia Florestal) - Universidade de Brasília, Brasília, 2001.         [ Links ]

BENITEZMALVIDO, J. Impact of forest fragmentation on seedling abundance in a tropical rain forest. Conservation Biology, v.12, n.2, p.380-389, 1998.         [ Links ]

BROWER, J. E.; ZAR, J. H.; von ENDE C. N. Field and laboratory methods for general ecology. Boston: Wm C Brown Publishers, 1990. 663 p.         [ Links ]

BURKE, D. M.; NOL, E. Edge and fragment size effects on the vegetation of deciduous forests on Ontario, Canada. Natural Areas Journal v.18, n.1, p.45-53, 1998.         [ Links ]

CADENASSO, M. L.; PICKETT, S. T. A. Linking edge structure to edge function: mediation of herbivore damage. Journal of Ecology, v.88, n.1, p.31-44, 2000.         [ Links ]

CAMARGO, J. L. C.; KAPOS, V. Complex edge effects on soil moisture and microclimate in central Amazonian forest. Journal of Tropical Ecology, v.11, n.1, p.205-211, 1995.         [ Links ]

CASENAVE, J. L.; PELLOTO, J. P.; PROTOMASTRO, J. Edgeinterior vegetation differences in vegetation structure and composition in a Chaco semiarid forest Argentina. Forest Ecology and Management, v.72, n.1, p.61-69, 1995.         [ Links ]

D'ANGELO, S. A. et al. Inferred causes of tree mortality in fragmented and intact Amazonian forests. Journal of Tropical Ecology, v.20, n.2, p.243-246, 2004.         [ Links ]

DAVIESCOLLEY, R. J.; PAYNE, G. W.; van ELSWIJK, M. Microclimate gradients across a forest edge. New New Zealand Journal of Ecology, v.24, n.2, p.111-121, 2000.         [ Links ]

DELGADO, J. D. et al. Edge effects of roads on temperature light canopy cover and canopy height in laurel and pine forests Tenerife Canary Islands. Landscape and Urban Planning, v.81, n.4, p.328-340, 2007.         [ Links ]

DIDHAM, R. K.; LAWTON, J. H. Edge structure determines the magnitude of changes in microclimate and vegetation structure in tropical forest fragments. Biotropica, v.31, n.1, p.17-30, 1999.         [ Links ]

ESSEEN, P. A. Tree mortality patterns after experimental fragmentation of an old growthconifer forest. Biological Conservation, v.68, n.1, p.19-28, 1994.         [ Links ]

FONTOURA, S. B.; GANADE, G.; LAROCCA, J. Changes in plant community diversity and composition across an edge between Araucaria forest and pasture in South Brazil. Revista Brasileira de Botanica, v.29, n.1, p.79-91, 2006.         [ Links ]

GEHLHAUSEN, S. M.; SCHWARTZ, M. W.; AUGSPURGER, C. K. Vegetation and microclimatic edge effects in two mixedmesophytic forest fragments. Plant Ecology, v.147, n.1, p.21-35, 2000.         [ Links ]

GENTRY, A. H. Diversity and floristic composition of neotropical dry forests. In: BULLOCK, S. H.; MOONEY, H. A.; MEDINA, E. (Ed.) Seasonally dry tropical forests. New York: Cambridge University Press, 1995.         [ Links ]

GILLESPIE, T. W.; GRIJALVA, A.; FARRIS, C. N. Diversity composition and structure of tropical dry forests in Central America. Plant Ecology, v.147, n.1, p.37-47, 2000.         [ Links ]

GOLDBLUM, D.; BEATTY, S. W. Influence of an old field/forest edge on a northeastern United States deciduous forest understory community. Journal of the Torrey Botanical Society, v.126, n.4, p.335-343, 1999.         [ Links ]

HANSSON, L. Edge structures and edge effects on plants and birds in ancient oakhazel woodlands. Landscape and Urban Planning, v.46, n.4, p.203-207, 2000.         [ Links ]

HERBST, M .J. M. et al. Edge effects and forest water use: A field study in a mixed deciduous woodland. Forest Ecology and Management, v.250, n.1, p.176-186, 2007.         [ Links ]

HOLBROOK, N. M.; WHITBECK, J. L.; MOONEY, H. A. Drought responses of neotropical dry forests trees . In: BULLOCK, S. H.; MOONEY, H. A.; MEDINA, E. (Ed.) Seasonally dry tropical forests. New York: Cambridge University Press, 1995. p.243-276         [ Links ]

HOLL, K. D.; LULOW, M. E. Effects of species habitat and distance from edge on postdispersal seed predation in a tropical rainforest. Biotropica, v.29, n.4, p.459-468, 1997.         [ Links ]

HURLBERT, S. H. Pseudoreplication and the design of ecological field experiments. Ecological Monographs, v.54, n.2, p.187-211, 1984.         [ Links ]

FUNDAÇÃO INSTITUTO BRASILEIRO DE GEOGRAFIA E ESTATÍSTICA IBGE. Zoneamento geoambiental e agroecológico do estado de Goiás região nordeste. Rio de Janeiro: 1995. (Série Estudos e Pesquisas em Geociências, 3)         [ Links ]

JANZEN, D. H. Management of habitat fragments in a tropical dry forest: growth. Annals of the Missouri Botanical Garden., v.75, n.1, p.105-116, 1988.         [ Links ]

JOSE, S. et al. Vegetation responses along edge-to-interior gradients in a high altitude tropical forest in peninsular India. Forest Ecology and Management, v.87, n.1, p.51-52, 1996.         [ Links ]

KAPOS, V. Effect of isolation on the water status of forest patches in the Brazilian Amazon. Journal of Tropical Ecology, v.5, n.1, p.173-185, 1989.         [ Links ]

KAPOS, V. et al. ¶ 13C as an indicator of edge effects in tropical rainforest reserves. Journal of Ecology, v.81, n.3, p.425-432, 1993.         [ Links ]

LAURANCE, W. F. Edge effect in tropical forest fragments application of a model for the design of nature reserves. Biological conservation, v.57, n.2, p. 205-219, 1991.         [ Links ]

LAURANCE, W. F. Do edge effects occur over large spatial scales? Trends in Ecology & Evolution, v.15, n.1, p.134-135, 2000.         [ Links ]

LAURANCE, W. F. et al. Rain forest fragmentation and the proliferation of successional trees. Ecology, v.87, p.469482, 2006.         [ Links ]

LAURANCE, W. F.; BIERREGAARD, R. O. Tropical forest remnants ecology management and conservation of fragmented communities. Chicago: Chicago University Press, 1997. 616p.         [ Links ]

LAURANCE, W. F. et al. Rain forest fragmentation and the dynamics of Amazonian tree communities. Ecology v.79, n.6, p.20322040, 1998.         [ Links ]

LAWES, M. J.; LAMB, B. C. C.; BOUDREAU, S. Area but no edgeeffect on woody seedling abundance and species richness in old Afromontane forest fragments. Journal of Vegetal Science, v.16, n.4, p.363-372, 2005.         [ Links ]

LERDAU, M.; WHITBECK, J.; HOLBROOK, N. M. Tropical Deciduous Forest death of a biome. Trends in Ecology & Evolution, v.6, n.7, p.201-202, 1991.         [ Links ]

LOVEJOY T. E. et al. Ecological dynamics of tropical forest fragments. In: SUTTON, S. L.; WHITMORE, T. C.; CHADWICK, A. C. (Ed.) Tropical rain forest ecology and management. London: Blackwell Scientific Publications, 1983.         [ Links ]

LUÍZ, G. C. Estudo do impacto ambiental a partir da análise espaço-temporal - Caso da região Vão do Paranã GO. Dissertação (Mestrado em Geociências) - Universidade Federal de Goiás, Goiânia, 1998.         [ Links ]

MALCOLM, J. R. Edge effects in central amazonian forest fragments. Ecology, v.75, n.8, p.2438-2445, 1994.         [ Links ]

MARGURRAN, A. E. Ecological diversity and its measurements. London: Croom Helm, 1988. 179p.         [ Links ]

MATLACK, G. R. Vegetation dynamics of the forest edge trends in space and sucessional time. Journal of Ecology, v.82, n.1, p.113123, 1994.         [ Links ]

MCDONALD, R. I.; URBAN, D. L. Forest edges and tree growth rates in the North Carolina Piedmont. Ecology v.85, n.8, p.2258-2266, 2004.         [ Links ]

MEDINA, E. Diversity of life forms of higher plants in neotropical dry forests. In: BULLOCK, S. H.; MOONEY, H. A.; MEDINA, E. (Ed.) Seasonally dry tropical forests, New York: Cambridge University Press, 1995. p.221242         [ Links ]

MURCIA, C. Edge effects in fragmented forest implications for conservation. Trends in Ecology & Evolution, v.10, n.1, p.58-62, 1995.         [ Links ]

NAVACRUZ, Y. et al. Evaluación del efecto de borde sobre dos especies del bosque tropical caducifolio de Jalisco México. Agrociencia, v.41, n.1, p.111-120, 2007.         [ Links ]

OLIVEIRA FILHO, A. T. et al. Variações estruturais do compartimento arbóreo de uma floresta semidecídua altomontana na chapada das Perdizes Carrancas, MG. Revista Brasileira de Botanica, v.27, n.2, p.291-309, 2004.         [ Links ]

OLIVEIRA FILHO A. T.; MELLO, J. M.; SCOLFORO, J. R. S. Effects of past disturbance and edges on tree community structure and dynamics within a fragment of tropical semideciduous forest in southeastern Brazil over a five years period 19871992. Plant Ecology, v.131, n.1, p.45-66, 1997.         [ Links ]

OLUPOT, W. A variable edge effect on trees of Bwindi Impenetrable National Park, Uganda, and its bearing on measurement parameters. Conservation Biology, v.142, n.4, p.789-797, 2009.         [ Links ]

PALIK, B. J.; MURPHY, P. G. Disturbance versus edge effects in SugarMaple/Beech forest fragments. Forest Ecology and Management, v.32, n.2-4, p.187-202, 1990.         [ Links ]

PHILLIPS, O. L.; ROSE, S.; MENDOZA, A. M. et al. Resilience of Southwestern Amazon Forests to Anthropogenic Edge Effects. Conservation Biology, v.20, n.6, p.1698-1710, 2006.         [ Links ]

POHLMAN, C. L.; TURTON, S. M.; GOOSEM M. Temporal variation in microclimatic edge effects near powerlines, highways and streams in Australian tropical rainforest. Agricultural and Forest Meteorology, v.149, n.4, p.84-95, 2009.         [ Links ]

RODRIGUES, E. Edge effects on the regeneration of forest fragments in south Brazil. 1998. NUMERO DE FOLHAS. (Tese PhD) - Harvard University, Cambridge, 1998.         [ Links ]

SAMPAIO, A. B.; HOLL, K. D.; SCARIOT, A. Regeneration of Seasonal Deciduous Forest Tree Species in LongUsed Pastures in Central Brazil. Biotropica, v.39, n.5, p.655-659, 2007.         [ Links ]

SAUNDERS, D. A.; HOBBS, R. J.; MARGULES, C. R. Biological consequences of ecosystem fragmentation: a review. Conservation Biology, v.5, n.1, p.18-32, 1991.         [ Links ]

SCARIOT, A.; SEVILHA, A. C. Diversidade Estrutura e manejo de florestas deciduais e as estratégias para a conservação. In: CAVALCANTI, T. B.; WALTER, B. M. T. (Ed.) Tópicos atuais em botânica: palestras convidadas do 51º Congresso Nacional de Botânica. Brasília: Recursos Genéticos e Biotecnologia, 2000.         [ Links ]

SCARIOT, A Forest fragmentation effects on palm diversity in central Amazonia. Journal of Ecology, v.87, n.1, p.66-76, 1999.         [ Links ]

SONG, S. J.; HANNON, S. J. Predation in heterogeneous forests: A comparison at natural and anthropogenic edges. Ecoscience, v.6, n.4, p.521-530, 1999.         [ Links ]

STATSOFT INC. STATISTICA for Windows [Computer program manual]. Tulsa: 2000.         [ Links ]

TABACHNICK, B. G.; FIDELL, L. S. Using multivariate statistics. Boston: Harper Collins Publishers, 1989. 980p         [ Links ]

TER BRAAK, C. J. F. The analysis of vegetation-environment relationships by canonical correspondence analysis. Vegetatio, v.69, n.1, p.69-77, 1987.         [ Links ]

VIEIRA, D. L. M.; SCARIOT, A. Principles of natural regeneration of tropical dry forests for restoration. Restoration Ecology, v.14, n.1, p.11-20, 2006.         [ Links ]

VIEIRA, D. M. et al. Tropical dry forest regeneration from root suckers in Central Brazil. Journal of Tropical Ecology, v.22, n.1, p.1-5, 2006.         [ Links ]

von ENDE, C. N. Repeated Measures Analysis growth and other timedependent measures. In: SCHEINER, S. M.; GUREVITCH, J. (Ed.) Design and analysis of ecological experiments. New York: Chapman and Hall, 1993. p.113-137.         [ Links ]

WHITMORE, T. C. Tropical forest disturbance disappearence and species loss. In: LAURANCE, W. F.; BIERREGAARD, R. O. (Ed.) Tropical forest remnants ecology management and conservation of fragmented communities. Chicago: Chicago University Press, 1997. p.3-12.         [ Links ]

WHITNEY, G. G.; RUNKLE, J. R. Edge versus age effects in the development of a beechmaple forest. Oikos, v.37, p.377-381, 1981.         [ Links ]

WILLIAMS-LINERA, G. Origin and development of forest edge vegetation in Panama. Biotropica, v.22, n.3, p.235-241, 1990a.         [ Links ]

WILLIAMS-LINERA, G. Vegetation structure and environmental conditions of forest edges in Panamá. Journal of Ecology, v.78, n.2, p.356373, 1990b.         [ Links ]

WILLIAMS-LINERA, G.; DOMINGUEZGASTELU, V.; GARCIAZURITA, M. Microenvironment and floristics of different edges in a fragmented tropical rainforest. Conservation Biology, v.12, n.5, p.1091-1102, 1998.         [ Links ]

WILSON M. F.; CROME F. H. J. Patterns of seed rain at the edge of a tropical Queensland rain forest. Journal of Tropical Ecology, v.5, n.3, p.301-308, 1989.         [ Links ]

WONG, T. C. M.; SODHI, N. S.; TURNER, I. M. Artificial nest and seed predation experiments in tropical lowland rainforest remnants of Singapore. Conservation Biology., v.85, n.1, p.97-104, 1998.         [ Links ]

ZAR, J. H. Biostatistical analysis. 4.ed. New York: PrenticeHall, 1999.         [ Links ]


Recebido em 21.09.2009 e aceito para publicação em 02.05.2011.

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License