Tropical forest degradation in the context of climate change: increasing role and research challenges. [K-2215-01]

While developed countries in temperate regions faced their forest transition about 100 years ago or more, “tropical forest rich” nations still largely depend on forest resources or land clearing for their development. Hence, tropical forests are retreating at an alarming rate from advancing cash crops, such as oil palm, soybean, or cattle ranching. Beside tropical deforestation, tropical forest degradation resulting mostly from human-induced causes (e.g. predatory or illegal logging, non-timber forest product extraction, fuel wood extraction) significantly contributes to greenhouse gas emissions and loss of biodiversity. If deforestation is an obvious ecosystem change, forest degradation is more difficult to discern and quantify. Degraded forests have become a major component of today's tropical landscapes, representing up to 50 % of all tropical forests. For example, almost half of standing primary tropical forests, up to 400 million ha, are designated by national forest services for timber production. The portion of tropical forests managed for timber extraction, hereafter referred to as “managed forests”, will therefore play key roles in the trade-off between provision of goods and maintenance of carbon stocks, biodiversity, and other services. However, so far, most of our understanding of tropical forest arise from studies carried out in old-growth undisturbed forests, or secondary forests (i.e. regrowth forests) while the ecology of degraded forests at the regional and continental scale remains poorly studied and their role to mitigate climate change still very poorly known. However, understanding the functions played by degraded forests in providing goods and environmental services in the context of climate change is crucial. We will first discuss the complex concept of forest degradation in the tropics and then define degraded forests. We will show their importance in providing timber while maintaining high levels of biodiversity and carbon stocks. We will further demonstrate that implementation of sustainable forest management can promote long term provision of ecosystem services. Finally, the potential of tropical degraded forests in mitigating climate change will be discussed along with future research challenges on this issue. (Texte intégral

Dynamics and persistence in a metacommunity centred on the plant Antirrhinum majus : theoretical predictions and an empirical test

International audience1. Spatial processes have a major influence on the stability of species interaction networks and their resilience to environmental fluctuations. Here, we combine field observations and a dynamic model to understand how spatial processes may affect a network composed of the flowering plant Antir-rhinum majus, its cohort of pollinators, and a specialist seed-predator and its parasitoid.2. The interactions taking place within this system were investigated by determining the fate of flowers and fruits on flowering and fruiting stems at 16 study sites. We then used this information to estimate spatial and temporal variation in the pollination rate, parasitism rate and hyperparasitism rate.3. We found that the plants were pollinator-limited, with relatively variable fruit-to-flower ratios across sites. On almost all sites, plants were both parasitized and hyperparasitized, at a low to moderate rate.4. Comparing our field observations with a tritrophic Nicholson-Bailey model, we found that empirical data are not always consistent with the conditions for local tritrophic persistence. This suggests that other mechanisms such as random disturbances and recolonizations (patch dynamics) or inter-site migration through metacommunity dynamics (source-sink dynamics) play a role in this system. Model simulations showed that dispersal could contribute to increasing tritrophic persistence in this system, and that source-sink structure, not just environmental stochasticity, may cause the observed pattern of spatial variation.5. Synthesis. We defined and measured metrics related to species interactions and densities. This led us to suggest that the functioning of the A. majus metacommunity is more consistent with source-sink than patch metacommunity dynamics, highlighting the extent to which dispersal explains the persistence of the system

Censusing and Measuring Lianas: A Quantitative Comparison of the Common Methods

Lianas contribute to many aspects of tropical forest diversity and dynamics, and interest in liana ecology has grown substantially in recent years. Methods to census lianas and estimate biomass, however, differ among studies, possibly hindering attempts to compare liana communities. At Nouragues Research Station (French Guiana), we tested the extent to which liana abundance, basal area, and estimated biomass differed depending on stem diameter measurement location, inclusion of ramets, inclusion of lianas rooted within versus passing through the plot, and plot shape. We found that the mean per plot abundance and basal area of lianas were significantly greater when lianas were measured low on the stem, when ramets were included, and when lianas were sampled in transects (2 × 50 m) than in square plots (10 × 10 m). Mean per plot liana abundance and basal area were 21 percent and 58 percent greater, when stems were measured at the largest spot on the stem compared to 130 cm from the ground, respectively. Including liana ramets increased average per plot liana abundance, basal area, and estimated biomass by 19, 17, and 16 percent, respectively. To facilitate cross‐study comparisons, we developed conversion equations that equate liana abundance, diameter, and basal area based on the measurements taken at four different stem locations. We tested these equations at Lambir Hills National Park, Malaysia and found that they did not differ significantly between the two sites, suggesting that the equations may be broadly applicable. Finally, we present a new allometric equation relating diameter and biomass developed from 424 lianas from five independent data sets collected in four countries

Modelling forest–savanna mosaic dynamics in man-influenced environments: effects of fire, climate and soil heterogeneity

Forests and savannas are the major ecotypes in humid tropical regions. Under present climatic conditions, forest is in a phase of natural expansion over savanna, but traditional human activities, especially fires, have strongly influenced the succession. We here present a new model, FORSAT, dedicated to the forest–savanna mosaic on a landscape scale and based on stochastic modelling of key processes (fire and succession cycle) and consistent with common field data. The model is validated by comparison between the qualitative emergent behaviour of the model and results of biogeographical field studies. Three types of forest succession are shown: progression of the forest edge, formation and coalescence of clumps in savanna and global afforestation of savanna. The parameters (frequency of savanna fires, climate and soil fertility) appear to have comparable effects and there is a sharp threshold between a forest edge progression scenario and the cluster formation one. Moreover, pioneer seed dispersal pattern and recruitment are determinant: peaked curves near a seed source and far dispersal combine to increase the fitness of the pioneers

Finite time and asymptotic behaviour of the maximal excursion of a random walk

We evaluate the limit distribution of the maximal excursion of a random walk in any dimension for homogeneous environments and for self-similar supports under the assumption of spherical symmetry. This distribution is obtained in closed form and is an approximation of the exact distribution comparable to that obtained by real space renormalization methods. Then we focus on the early time behaviour of this quantity. The instantaneous diffusion exponent $\nu_n$ exhibits a systematic overshooting of the long time exponent. Exact results are obtained in one dimension up to third order in $n^{-1/2}$. In two dimensions, on a regular lattice and on the Sierpi\'nski gasket we find numerically that the analytic scaling $\nu_n \simeq \nu+A n^{-\nu}$ holds.Comment: 9 pages, 4 figures, accepted J. Phys.