Tropical forests store large amounts of carbon and high biodiversity, but are being degraded at alarming rates. The emerging global Forest and Landscape Restoration (FLR) agenda seeks to limit global climate change by removing carbon dioxide from the atmosphere through the growth of trees. In doing so, it may also protect biodiversity as a free cobenefit, which is vital given the massive shortfall in funding for biodiversity conservation. We investigated whether natural forest regeneration on abandoned pastureland offers such cobenefits, focusing for the first time on the recovery of taxonomic diversity (TD), phylogenetic diversity (PD) and functional diversity (FD) of trees, including the recovery of threatened and endemic species richness, within isolated secondary forest (SF) fragments. We focused on the globally threatened Brazilian Atlantic Forest, where commitments have been made to restore 1 million hectares under FLR. Three decades after land abandonment, regenerating forests had recovered ~20% (72 Mg/ha) of the above‐ground carbon stocks of a primary forest (PF), with cattle pasture containing just 3% of stocks relative to PFs. Over this period, SF recovered ~76% of TD, 84% of PD and 96% of FD found within PFs. In addition, SFs had on average recovered 65% of threatened and ~30% of endemic species richness of primary Atlantic forest. Finally, we find positive relationships between carbon stock and tree diversity recovery. Our results emphasize that SF fragments offer cobenefits under FLR and other carbon‐based payments for ecosystem service schemes (e.g. carbon enhancements under REDD+). They also indicate that even isolated patches of SF could help to mitigate climate change and the biodiversity extinction crisis by recovering species of high conservation concern and improving landscape connectivity.
Summary1. Fragmentation of tropical forests is a major driver of the global extinction crisis. A key question is understanding how fragmentation impacts phylogenetic diversity, which summarizes the total evolutionary history shared across species within a community. Conserving phylogenetic diversity decreases the potential of losing unique ecological and phenotypic traits and plays important roles in maintaining ecosystem function and stability. 2. Our study was conducted in landscapes within the highly fragmented Brazilian Atlantic forest. We sampled living trees with d.b.h. ≥ 4.8 cm in 0.1 ha plots within 28 fragment interiors and 12 fragment edges to evaluate the impacts of landscape configuration, composition and patch size, as well as edge effects, on phylogenetic diversity indices (PD, a measure of phylogenetic richness; MPD, phylogenetic distance between individuals in a community in deep evolutionary time; and MNTD, phylogenetic distance between each individual and its nearest phylogenetic neighbour). 3. We found that PD and MPD were correlated with species richness, while MNTD was not. Best models suggest that MPD was positively related to edge density and negatively related to the number of forest patches, but that there was no effect of landscape configuration and composition metrics on PD or MNTD, or on standardized values of phylogenetic structure (sesPD, sesMPD and sesMNTD), which control for species richness. Considering all selected models for phylogenetic diversity and structure, edge density and number of forest patches were most frequently selected. 4. With increasing patch size, we found lower PD in interiors but no change at edges and lower sesMNTD regardless of habitat type. Additionally, PD and sesMNTD were higher in interiors than at edges. 5. Synthesis. Changes in MPD and sesMNTD suggest that extirpation of species at edges or in highly fragmented landscapes increases the dominance of species within a subset of clades (phylogenetic clustering), likely those adapted to disturbance. Smaller patch sizes are phylogenetically diverse and overdispersed, probably due to an invasion of edge-adapted species. Conservation must enhance patch area and connectivity via forest restoration; pivotally, even small forest patches are important reservoirs of phylogenetic diversity in the highly threatened Brazilian Atlantic forest.
Context: The sandy-savanna ecosystem "Mussununga", a natural ecosystem that occurs as patches throughout the Atlantic Forest domain, is threatened by anthropogenic factors and biological invasions of Australian Acacia species. Habitat degradation in the Atlantic Forest domain and extensive road networks could facilitate Acacia invasion into Mussununga. Objectives: We investigated whether: (a) landscape permeability (measured by effective conductance) facilitates Acacia invasion; (b) forest fragments are barriers, and roads and highways are corridors for invasive spread of Acacia; and (c) size and shape of Mussununga patches play a role in biological invasion. Methods: Acacia invasion was investigated in 32 Mussununga sites within the Atlantic Forest domain. We tested the effect of a set of landscape permeability scenarios based on circuit analysis and nine other metrics of landscape structure on Acacia occurrence using three buffer-zone sizes (0.5, 1, and 2 km). Results: The likelihood of Acacia invasion significantly increased with landscape permeability. The best-fitting landscape permeability scenario designated road networks as corridors, intact forests and water surfaces as barriers, and degraded habitats as non-barriers. We also found that Mussununga areas within a 0.5 km buffer negatively affected the biological invasion by Acacia. Conclusions: Extensive habitat degradation by deforestation and dense road networks facilitate Acacia invasion into sandy-savanna Mussununga ecosystems. Landscape permeability may be used as a risk-assessment tool for biological invasion by Acacia species. Mussununga patches can be protected from Acacia invasion | 599 Applied Vegetation Science HERINGER Et al.
Under the UN-Decade of Ecosystem Restoration and Bonn Challenge, second-growth forest is promoted as a global solution to climate change, degradation and associated losses of biodiversity and ecosystem services. Second growth is often invaded by alien tree species and understanding how this impacts carbon stock and biodiversity recovery is key for restoration planning. We assessed carbon stock and tree diversity recovery in second growth invaded by two
Acacia
species and non-invaded second growth, with associated edge effects, in the Brazilian Atlantic Forest. Carbon stock recovery in non-invaded forests was threefold lower than in invaded forests. Increasingly isolated, fragmented and deforested areas had low carbon stocks when non-invaded, whereas the opposite was true when invaded. Non-invaded forests recovered threefold to sixfold higher taxonomic, phylogenetic and functional diversity than invaded forest. Higher species turnover and lower nestedness in non-invaded than invaded forests underpinned higher abundance of threatened and endemic species in non-invaded forest. Non-invaded forests presented positive relationships between carbon and biodiversity, whereas in the invaded forests we did not detect any relationship, indicating that more carbon does not equal more biodiversity in landscapes with high vulnerability to invasive acacias. To deliver on combined climate change and biodiversity goals, restoration planning and management must consider biological invasion risk.
This article is part of the theme issue ‘Understanding forest landscape restoration: reinforcing scientific foundations for the UN Decade on Ecosystem Restoration’.
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