Journal of Tropical Ecology 

About: Journal of Tropical Ecology is an academic journal published by Cambridge University Press. The journal publishes majorly in the area(s): Species richness & Seed dispersal. It has an ISSN identifier of 0266-4674. Over the lifetime, 2191 publications have been published receiving 92623 citations.

Tropical secondary forests

Abstract: The literature on tropical secondary forests, defined as those resulting from human disturbance (e.g. logged forests and forest fallows), is reviewed to address questions related to their extent, rates of formation, ecological characteristics, values and uses to humans, and potential for management. Secondary forests are extensive in the tropics, accounting for about 40% of the total forest area and their rates of formation are about 9 million ha yr−1. Geographical differences in the extent, rates of formation and types of forest being converted exist.Secondary forests appear to accumulate woody plant species at a relatively rapid rate but the mechanisms involved are complex and no clear pattern emerged. Compared to mature forests, the structure of secondary forest vegetation is simple, although age, climate and soil type are modifying factors. Biomass accumulates rapidly in secondary forests, up to 100 t ha−1 during the first 15 yr or so, but history of disturbance may modify this trend. Like biomass, high rates of litter production are established relatively quickly, up to 12–13 t ha−1 yr−1 by age 12–15 yr. And, in younger secondary forests (< 20 yr), litter production is a higher fraction of the net primary productivity than stemwood biomass production. More organic matter is pro duced and transferred to the soil in younger secondary forests than is stored in above-ground vegetation. The impact of this on soil organic matter is significant and explains why the recovery of organic matter in the soil under secondary forests is relatively fast (50 yr or so). Nutrients are accumulated rapidly in secondary vegetation, and are returned quickly by litterfall and decomposition for uptake by roots.We propose a model of the gains and losses, yields and costs, and benefits and tradeoffs to people from the current land-use changes occurring in the tropics. When the conversion of forest lands to secondary forests and agriculture is too fast or land-use stages are skipped, society loses goods and services. To avoid such a loss, we advocate management of tropical forest lands within a landscape perspective, a possibility in the tropics because land tenures and development projects are often large.

Effects of isolation on the water status of forest patches in the Brazilian Amazon

Abstract: Patterns of edge-related environmental changes and plant water relations were investigated in the isolated forest reserves of the INPA-WWF Minimum Critical Size of Eco-systems project near Manaus, Brazil early in the wet season.

Common allometric equations for estimating the tree weight of mangroves

Abstract: Inventory data on tree weights of 104 individual trees representing 10 mangrove species were collected from mangrove forests in South-East Asia to establish common allometric equations for the trunk, leaf, above-ground and root weight. We used the measurable tree dimensions, such as dbh (trunk diameter at breast height), DR0.3 (trunk diameter at 30 cm above the highest prop root of Rhizophora species), DB (trunk diameter at lowest living branch), and H (tree height) for the independent variable of equations. Among the mangrove species studied, the trunk shape was statistically identical regardless of site and species. However, ρ (wood density of tree trunk) differed significantly among the species. A common allometric equation for trunk weight was derived, when dbh2H or DR0.32H was selected as the independent variable and wood density was taken into account. The common allometric equations for the leaf and the above-ground weight were also derived according to Shinozaki's pipe model and its extended theory. The common allometric relationships for these weights were attained with given ρ of each species, when DB2 or dbh2 or DR0.32 was selected as the independent variable. For the root weight, the common equation was derived from the allometric relationship between root weight and above-ground weight, since these two partial weights significantly correlated with each other. Based on these physical and biological parameters, we have proposed four common allometric equations for estimating the mangrove tree weight of trunk, leaf, above-ground part and root.

Fire as a large-scale edge effect in Amazonian forests.

Abstract: Amazonian forests are being rapidly cleared, and the remaining forest fragments appear unusually vulnerable to fire. This occurs because forest remnants have dry, fire-prone edges, are juxtaposed with frequently burned pastures, and are often degraded by selective logging, which increases forest desiccation and fuel loading. Here we demonstrate that in eastern Amazonia, fires are operating as a large-scale edge effect in the sense that most fires originate outside fragments and penetrate considerable distances into forest interiors. Multi-temporal analyses of satellite imagery from two frontier areas reveal that fire frequency over 12-14-y periods was substantially elevated within at least 2400 m of forest margins. Application of these data with a mathematical core-area model suggests that even large forest remnants (up to several hundred thousand ha in area) could be vulnerable to edge-related fires. The synergistic interactions of forest fragmentation, logging and human-ignited fires pose critical threats to Amazonian forests, particularly in more seasonal areas of the basin.

The dynamics of tree populations in tropical forest: a review.

Abstract: Published work on the dynamics of forest tree recruitment, growth and mortality in natural tropical forest is reviewed. In most forests studied, annual mortality is between 1% and 2% and is independent of size class in trees >10 cm dbh; mortality is negatively correlated with growth rate and crown illumination; growth rate is highly variable between individual trees, but shows strong autocorrelation between successive measurements on the same tree. Differences in the rate of dynamic processes can be detected between some species at a site, but data are presently insufficient to determine whether these differences are preserved at other sites where the species occur. None of the studies discussed are of sufficient duration to permit us to draw any conclusions about the equilibrium or non-equilibrium of floristic composition.