Land-use change occurs nowhere more rapidly than in the tropics, where the imbalance between deforestation and forest regrowth has large consequences for the global carbon cycle. However, considerable uncertainty remains about the rate of biomass recovery in secondary forests, and how these rates are influenced by climate, landscape, and prior land use. Here we analyse aboveground biomass recovery during secondary succession in 45 forest sites and about 1,500 forest plots covering the major environmental gradients in the Neotropics. The studied secondary forests are highly productive and resilient. Aboveground biomass recovery after 20 years was on average 122 megagrams per hectare (Mg ha(-1)), corresponding to a net carbon uptake of 3.05 Mg C ha(-1) yr(-1), 11 times the uptake rate of old-growth forests. Aboveground biomass stocks took a median time of 66 years to recover to 90% of old-growth values. Aboveground biomass recovery after 20 years varied 11.3-fold (from 20 to 225 Mg ha(-1)) across sites, and this recovery increased with water availability (higher local rainfall and lower climatic water deficit). We present a biomass recovery map of Latin America, which illustrates geographical and climatic variation in carbon sequestration potential during forest regrowth. The map will support policies to minimize forest loss in areas where biomass resilience is naturally low (such as seasonally dry forest regions) and promote forest regeneration and restoration in humid tropical lowland areas with high biomass resilience.

Light regimes beneath closed canopies and tree-fall gaps are compared for five temperate and tropical forests using fish-eye photography of intact forest canopies and a model for calculating light penetration through idealized gaps. Beneath intact canopies, analyses of canopy photographs indicate that sunflecks potentially contribute 37–68% of seasonal total photosynthetically active radiation. In all of the forests, potential sunfleck duration is brief (4–6 min), but the frequency distributions of potential sunfleck duration vary because of differences in canopy geometry and recent disturbance history. Analysis of the photographs reveals that incidence angles for photosynthetically active radiation beneath closed canopies are not generally vertical for any of the forests, but there was considerable variation both among and within sites in the contribution of overhead versus low-angle lighting. Calculations of light penetration through idealized single-tree gaps in old growth Douglas-fir – hemlock forests indicate that such gaps have little effect on understory light regimes because of the high ratio of canopy height to gap diameter. However, single-tree gaps in the other four forest types produce significant overall increases in understory light levels. There is also significant spatial variation in seasonal total radiation in and around single-tree gaps. Our results demonstrate that there can be significant penetration of light into the understory adjacent to a gap, particularly at high latitudes. As gap size increases, both the mean and the range of light levels within the gap increases, but even in large gaps (ca. 1000 m2) the potential duration of direct sunlight is generally brief (<4 h). The major differences in gap light regimes of the five forests are largely a function of canopy height and latitude. The effects of latitude should also result in differences in gap light regimes across the geographic range of individual forest types.

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The abundance and diversity of lianas were examined along a tropical forest chronosequence at the Barro Colorado Nature Monument, Panama. Lianas ≥0.5 cm diameter were sampled along transects in two replicated stands in secondary (20, 40, 70 and 100 y after abandonment) and old-growth (>500 y) forests. Ordination of stands based on relative abundance, but not presence-absence, showed a significant separation of stands by age. Lianas were significantly more abundant and diverse (Fisher's α) in younger forests (20 and 40 y) than in older forests (70 and 100 y, and old-growth). The decline in liana abundance with stand age was offset by increased mean basal area per individual, resulting in a relatively constant total basal area and estimated biomass across stand age. The proportions of tendril climbers decreased and stem twiners increased over stand age. Decline in liana abundance and changes in liana composition may be related to changes in support and light availability. Although lianas are recognized as playing an important role in the early secondary sucession of many tropical forests, these results have shown that their important contribution to total basal area and biomass can continue as the forest matures, even as the numbers of established lianas declines.