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Assessment, Conservation and Sustainable Use of Forest Biodiversity

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Keynote Addresses<br />

Recent research <strong>and</strong> development work being carried out by CATIE <strong>and</strong> its national partners in natural<br />

Central American timber production forests has the goals <strong>of</strong> increasing knowledge <strong>of</strong> forest management<br />

effects on biodiversity – with emphasis on the surprisingly poorly-documented area <strong>of</strong> species- <strong>and</strong> geneticlevel<br />

diversity <strong>of</strong> tree communities <strong>and</strong> populations – <strong>and</strong> on the development <strong>of</strong> adaptive ecological<br />

components <strong>of</strong> national st<strong>and</strong>ards for sustainable forest management at the fmu level. This work, possibly<br />

uniquely in the tropics, takes into account that Central American production forests are also, increasingly,<br />

fragmented forests. Work towards the twin goals is closely integrated. The focus is on two moist forest<br />

ecoregions as defined by Dinerstein et al. (1995): the Central American Atlantic forest <strong>and</strong> the Tehuantepec<br />

forest. Besides embracing some <strong>of</strong> the largest remnant forest areas <strong>of</strong> Central America, these ecoregions are<br />

major sources <strong>of</strong> forest products <strong>and</strong> are a key component <strong>of</strong> the area <strong>of</strong> the Mesoamerican Biological<br />

Corridor, a major conservation strategy currently being implemented with support from governments <strong>and</strong><br />

international organizations. We emphasize that this research focuses on managed forests, not on forests<br />

subjected to conventional logging.<br />

Taxonomic biodiversity at the species level is usefully characterized in terms <strong>of</strong> both the species diversity <strong>and</strong> the<br />

species composition <strong>of</strong> the forest community <strong>and</strong> our work is carried out in permanent sample plots with<br />

planning for the long term. As a large proportion <strong>of</strong> the plant diversity <strong>of</strong> tropical rain forests is found among<br />

life forms other than large trees, this characterization should embrace a broader spectrum <strong>of</strong> the community<br />

than is the case in traditional permanent sample plot studies. CATIE has introduced methodological<br />

innovations to take this latter necessity into account, sampling the forest understorey as well as individuals ≥ 10<br />

cm dbh.<br />

For the analysis <strong>of</strong> management effects on plant taxonomic biodiversity, our results show that in general, it is<br />

convenient to identify both direct <strong>and</strong> indirect effects. Direct effects are immediate consequences <strong>of</strong><br />

management operations <strong>and</strong> occur simply because some plants in sample plots are killed by those operations.<br />

Indirect effects <strong>of</strong> management operations on plant biodiversity may occur as consequences <strong>of</strong> managementinduced<br />

changes in forest environmental conditions or in ecological processes such as pollination or seed<br />

dispersal. These effects will evolve over time <strong>and</strong> may be long-lasting.<br />

Direct effects <strong>of</strong> management on plant species richness are relatively simple to demonstrate. Speciesabundance<br />

distributions in our permanent sample plots are typical <strong>of</strong> those for tropical forests in that they<br />

show large numbers <strong>of</strong> species represented by few or single individuals. Some <strong>of</strong> these individuals are killed<br />

when forests are logged or silvicultural treatments applied, these deaths bringing about immediate reductions<br />

in the species-richness <strong>and</strong> diversity <strong>of</strong> the vegetation in the plot. It is important to point out that such<br />

reductions <strong>of</strong> diversity are to an extent artefacts <strong>of</strong> the permanent sample plot techniques used <strong>and</strong> by their<br />

very nature, certainly do not mean that species are being locally extinguished. Indirect effects require<br />

demonstration by more detailed studies, though it may be inferred that such changes are taking place<br />

especially if appropriate methodologies for the study <strong>of</strong> mortality are used. In intensive research in three<br />

different floristic types <strong>of</strong> production forest in the Central American Atlantic moist forest CATIE has found,<br />

however, that in spite <strong>of</strong> the array <strong>of</strong> factors which may influence it in timber production forests, plant species<br />

diversity is not reduced during the first decade <strong>of</strong> management. This conclusion applies over a range <strong>of</strong><br />

harvesting intensities from 10 – 30 m 3 ha -1 <strong>and</strong> to forest st<strong>and</strong>s where silvicultural treatment has produced<br />

major changes in forest structure <strong>and</strong> marked increases in the growth <strong>of</strong> potential crop trees. Two hundredyear<br />

simulations using Gavilán, an individual-tree computer model developed at CATIE (Sitoe 2000), further<br />

support the tentative conclusion that plant species diversity is a robust forest characteristic in the context <strong>of</strong><br />

management interventions typical <strong>of</strong> Central American production forests, <strong>and</strong> that sustainable production<br />

<strong>and</strong> the conservation <strong>of</strong> a large proportion <strong>of</strong> the original plant taxonomic biodiversity are compatible.<br />

<strong>Forest</strong> composition <strong>and</strong> forest diversity may vary independently (Finegan 1996) <strong>and</strong> it remains a possibility<br />

that compositional change occurs, for example if populations <strong>of</strong> plant species typical <strong>of</strong> the original forest<br />

decline or are locally extinguished under management, even if forest diversity is maintained. Speciesabundance<br />

distributions again rear their heads in the analysis <strong>of</strong> compositional change using permanent<br />

sample plot data, as changes in relative abundance can only be reliably identified for that minority <strong>of</strong> species<br />

which are, or become, relatively common. Our results for such species show that as may be expected, forest<br />

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