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1.1.4. MATERIALES DE REFUERZO

1.1.4.3. FIBRA DE VIDRIO [14]

5.1 Introduction

Changes in community trophic structure accompanying biodiversity loss are a

commonly observed outcome of tropical forest fragmentation. These changes are

important in influencing trajectories of ecosystem function as well as ecosystem

collapse of forest fragments.

A number of factors are thought to drive trophic structural changes in habitat

fragments generally. Area and isolation effects may drive differential species loss

from higher trophic levels resulting in shortening of food chain lengths in small habitat

fragments (Schoener 1989). Models developed by Holt (1996) mirror much empirical

observation in predicting that the slope of species-area relations should increase with

trophic rank. Biotic and abiotic edge effects of fragmentation can also influence

trophic structuring of rain forest communities via the sum of differential species

responses to microclimatic and other gradients. The type of matrix habitat surrounding

forest fragments may also have a profound influence on trophic structuring. In the case

of rain forest fragments surrounded by a terrestrial matrix, influx of disturbed habitat

species may be important. However, where the matrix habitat is aquatic, trophic

distortions affecting communities of tropical forest islands are known to be more

on species dispersion and mobility and their greater negative impact on persistence of

higher trophic levels.

Studies of changes in trophic structuring resulting from rain forest

fragmentation have largely focused on above- rather than below-ground food webs,

and upon vertebrates rather than invertebrates. Hence, the responses of decomposer

communities have been largely neglected. Yet decomposers of plant-derived organic

material are likely to be strongly directly affected by forest fragmentation due to the

phenomenon of biomass collapse.

An 18-year study of tree community structure and dynamics at the BDFFP has

shown that hotter, drier microclimatic conditions and greater exposure to wind, with

decreasing distance to forest edges, are responsible for increased tree mortality, and

consequent tree recruitment (Laurance et al. 1998). Laurance et a l (1997) have shown

that BDFFP forest fragments have undergone a net loss in biomass of around 10%

within two to four years of isolation, the time interval during which the rate of tree

die-off may be maximal. We might expect that the increased availability of dead plant

matter would present a resource bonanza for decomposer organisms that are able to

tolerate the negative influences of forest fragmentation. Changes in diversity and

abundance of decomposers surviving in forest fragments over time should have a

direct bearing on rates of breakdown of dead plant biomass and greenhouse gas

production. Moreover, we would expect these changes to have an impact on above­

ground food webs inside forest fragments.

This study presents data on the early effects of forest fragmentation on

functional group composition of the termite assemblage across the SEFP (for further

presented in order to establish the degree to which biotic and abiotic edge effects had

become established on islands at the time of termite sampling. In particular, the

evidence for tree-die off and consequent changes in canopy cover and availability of

dead wood are presented. The findings are compared with those of the BDFFP study

(De Souza and Brown 1994), particularly in the context of the profound differences in

the matrix habitats surrounding fragments at the two sites. Possible hypotheses to

explain the observed patterns are reviewed, and the implications for changes in

ecosystem function and carbon flux discussed.

5.2 Methods

TERMITE FEEDING GROUPS.

Following Donovan et a l (in press) we placed each species in the St. Eugène

assemblage into one of four feeding groups according to the morphological characters

of the workers indicating their position along the humification gradient of organic

matter decomposition. Using this classification, group I wood feeders feed on the least

humified substrates and group IV soil feeders feed on the most humified ones.

Additionally, a more fundamental level of feeding group distinction used was that

between wood and leaf-litter feeders (groups I and II combined) and soil feeders

ANALYSES

(i) Relationships between environmental variables across sites.

Logistic regression was used to analyse the apportionment of the total numbers of

large standing tree trunks (of >10 cm diameter above breast height) per transect,

between standing dead and live trunks combined, in relation to logio (distance to forest

edge) and logio (area), and to analyse the relationship between percentage canopy

cover and the same two fragmentation variables.

In order to control for any possible influence of the ghost forest termite

assemblage upon smaller island assemblages, all ghost forest species also found in

terrestrial transect samples were excluded from datasets, both of termite relative

encounters and species richness across sites.

(ii) Termite relative encounters across feeding groups in relation to environmental

variables.

Termite relative encounters were analysed at the levels of feeding group (I-IV) using

ordination methods. PCA was the indirect gradient method used, and RDA the direct

gradient method used to investigate the relative encounters of termites across feeding

groups in relation to environmental variable data collected at each of the 13 sites (see

Chapter 4, methods section). As in ordinations of species level data (Chapter 4),

partialling out of any effects of season on relative encounter data was achieved by

were partial analyses. Data for number of encounters within each feeding group were

logio (x + 1) - transformed prior to analyses. In the RDA, forward selection was used

to rank environmental variables in order of their importance in explaining variation in

relative encounters across feeding groups. Marginal eigenvalues were computed for

each environmental variable, and significance at each stage (i.e. for each variable

selected) was tested using a Monte Carlo permutation test with 999 random

permutations.

(iii) Relative encounters o f wood and soil feeding termites, and the whole assemblage,

in relation to environmental variables.

Linear regression was used to test the relationship between both main fragmentation

variables, logio (edge distance) and logic (fragment area), and logic (encounters) for

wood and leaf-litter feeders (groups I + II) and soil feeders (groups in + IV), and for

the total combined assemblage. Seasonality is known to influence abundance and

diversity of termite samples (Dibog et al. 1998). As termite sampling was carried out

in the rainy season for nine transects, and during the dry season for four transects, we

tested for significant effects of season upon species richness and logic (encounters).

Where season was shown to be significant, all regression analyses were performed

with season partialled out.

Forward stepwise multiple regression was used to determine which of the 17

environmental variables measured were significant predictors of logic (encounters)

and species richness for wood and leaf-litter feeders, soil feeders, and for the whole

used simply to see whether fragmentation variables, or uncorrelated environmental

gradients, were having the greatest influence on the distribution of logio (encounters)

and species richness between functional groups, and for the whole assemblage, across

sites.

5.3 Results

(i) Environmental variables.

Linear regressions against the two fragmentation variables produced significant results

for only three environmental variables in the case of logic (distance to forest edge),

with only two of these showing significance with logic (area) (Table 5.1). As logic

Table 5.1. Significant results of linear regressions of log] o (distance to forest edge) and logio (area) against 15 environmental variables, across 13 standardised transects (see also Figure 5.1).

Dependent variable: Independent variable: F d P Slope F-SMALL LGEDGE 13.42 1, 1 0.004 0.550 -v e F-SMALL LGAREA 6.70 1, 1 0.025 0.378 -v e V-STAND LGEDGE 5.06 1, 1 0.046 0.315 -v e MOISTURE LGEDGE 9.21 1, 1 0.011 0.456 +ve MOISTURE LGAREA 5.85 1, 1 0.034 0.347 +ve

(distance to forest edge) showed consistently stronger correlations with the

environmental variables than logic (area), it is the relationships with the former that

are presented graphically (Figure 5.1). The most significant correlation was with

frequency of small wood which showed a strongly negative, and approximately linear,

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