Resilience of lowland Atlantic forests in a highly fragmented landscape: Insights on the temporal scale of landscape restoration
Introduction
Tropical forests are hotspots for biodiversity and carbon conservation (Beer et al., 2010, Bonan, 2008, Myers et al., 2000). They are subject to several anthropogenic impacts, such as fragmentation, deforestation and selective logging (Malhi et al., 2014), which result in losses of biodiversity (Barlow et al., 2016, Bihn et al., 2008, Gibson et al., 2011, Laurance et al., 2002, Newbold et al., 2015) and large amounts of carbon in the form of the greenhouse gas CO2 (Baccini et al., 2017, Magnago et al., 2015). For these reasons, deforestation and degradation of tropical forests are especially harmful to the environment and ecosystem functioning (Malhi et al., 2002).
Human impacts have also increased the proportion of second-growth forests across the landscape (FAO, 2018). These secondary forests of different sizes play a crucial role in biodiversity conservation and carbon mitigation, but much debate on these issues and traditional research tend to revolve around mature forests (Gibson et al., 2011, Powers and Marín-Spiotta, 2017, Sullivan et al., 2017). Fortunately, the importance of secondary forests has been increasingly recognized in recent years (Bongers et al., 2015, Chazdon et al., 2016, Poorter et al., 2016), especially those forests able to naturally recover their structure and functions, representing resilient ecosystems (Safar et al., 2019, Willis et al., 2018).
Not all ecosystems are able to recover naturally after a disturbance ceases, because forest recovery and successional trajectory can be influenced by climate (Becknell et al., 2012, Toledo et al., 2011), soil properties (Pinho et al., 2018, Toledo et al., 2018), land use history (Fu et al., 2017, Jakovac et al., 2015) and the initial colonization (Chazdon, 2014). Since trees play a crucial role in the provision of ecosystem functions and services, such as the regulation of global carbon cycle (Bonan, 2008, Oliver et al., 2015), resilient forests ecosystems potentially offer a low-cost approach to climate change mitigation (Busch et al., 2019, Chazdon et al., 2016, Poorter et al., 2016) and biodiversity conservation (Ferreira et al., 2018, Phelps et al., 2012). For these reasons, the conservation of resilient ecosystems has been included in local and international environmental policies and targets inspired by the United Nations Framework Convention on Climate Change (UNFCCC) and the Convention on Biological Diversity (CBD).
There are several global and national efforts to maintain and enhance natural tropical ecosystems within Brazilian landscapes. For example, the Brazilian Atlantic Forest Restoration Pact (AFRP), launched in 2009, aims to promote the restoration of 15 million hectares of the forest by the year 2050 (Melo et al., 2013). Aligned with the Aichi Targets, the Brazilian Biodiversity Targets for 2020, adopted in 2013, aims to enhance ‘ecosystem resilience and the contribution of biodiversity to carbon stocks through conservation and restoration actions, including restoration of at least 15% of degraded ecosystems’ (Aichi Target 15, Strategic Plan for Biodiversity 2011–2020) (CBD, 2013, MMA, 2017). In 2015, the Brazilian government established the National REDD + Strategy (ENREDD +) in order to contribute to climate change mitigation by promoting forest conservation and recovery, and eliminating illegal deforestation by 2020 (MMA, 2016). In the following year, Brazil committed to restore 12 million hectares of land by the year 2030 under the Bonn Challenge, another global forest landscape restoration (FLR) initiative to restore degraded and deforested lands for biodiversity and carbon benefits that represents a practical means of achieving Biodiversity Targets and UNFCCC’s REDD + goals.
Understanding the capacity and the time needed for forests to recover from a disturbance might help to establish safe predictions about what would happen to these forests in different scenarios of environment impacts, and design effective conservation initiatives and investments. Yet, little is known about the recovery rate of the structure and tree composition of the Brazilian Atlantic Forest (see de Paula et al., 2015, Liebsch et al., 2008, Piotto et al., 2009), one of the most diverse and threatened tropical forest in the world (Myers et al., 2000), remaining only 12.4% of forest remnants above 3 ha (SOS Mata Atlântica, 2018). The long history of human occupation and exploitation in the Brazilian Atlantic forest resulted in highly fragmented landscapes, mainly composed of small fragments at some stage of recovery (Ribeiro et al., 2009).
Here we used a space-for-time substitution, or chronosequence approach, to investigate the resilience potential of Brazilian Atlantic forests in a landscape context using data from old-growth and second-growth forests of various ages. We studied the resilience of tree species, including those with high conservation value (endemic and globally threatened species), and the aboveground carbon storage. The definition of resilience adopted here is the capacity of an environment parameter (e.g. species richness) to return to pre-disturbance levels (Nimmo et al., 2015), i.e. the old-growth forests values (reference forests). To accomplish our main goal we (i) investigated whether tree species richness, species composition and carbon stock are recovering along the chronosequence at a landscape scale; (ii) assessed how much of the old-growth forest values the 20-yr-old secondary forests had attained, and (iii) estimated the absolute and relative time that second-growth forests take to approach the tree composition and mean old-growth forests values, used as a proxy of full recovery (100%). Then, we discuss the implications of our findings for biodiversity and carbon conservation and mitigation in human-modified landscapes under global and local initiatives for ecological restoration.
Section snippets
Study region
The study was conducted in Atlantic lowland rain forests located within or nearby the Reserva Biológica do Córrego Grande and the Floresta Nacional do Rio Preto, in northern Espírito Santo State (ES) and southern Bahia State (BA), Brazil (Fig. 1). The studied regions are part of the Bahia biogeographical sub region of the Atlantic Forest domain, proposed by da Silva and Casteleti (2003), which is the second best preserved sub region, holding 17.7% of the Atlantic forest original vegetation (
Results
We sampled a total of 1643 trees classified in 252 species of 53 families, including morphospecies (see Table A.2). Four individuals were completely unidentified, seven were only identified at family level and 14 to genus level. Of the species identified, 96 (38.1%) are endemic to the Atlantic Forest, 24 (9.5%) are threatened to some degree, and approximately 17% of the endemic species are classified as threatened at some degree. The most representative families were Annonaceae (182 trees),
Discussion
Our empirical assessment of the resilience of forest structure and diversity at landscape-scale represents a crucial step in understanding the behavior of Atlantic forests during natural regeneration and their potential use in passive restoration projects. This study addressed sites with different disturbance histories, which better represent the current Atlantic Forest landscape of the studied regions: a mosaic of old- and second-growth forest remnants and areas under different uses (e.g.
Conclusions
In the highly fragmented landscape of the Atlantic Forest Biome, a fast recovery of second-growth forests in terms of species richness was observed, suggesting that national targets for the restoration of forest biodiversity may be achieved by ceasing deforestation and allowing resilient ecosystems to regenerate naturally. On the other hand, species with high conservation value are not recovering along succession, while carbon stocks and tree composition would take the scale of hundreds to
Declaration of Competing Interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Acknowledgements
Many thanks to Carlos Aquila, Carla S. Guimarães, João Paulo Gusmão, Marco A. Peixoto, Moacir Rocha, Hugo Galvão, Natália Silva, Matheus and Gabriel Cóser for fieldwork support; Celso Antônio for laboratory assistance; Suzano Papel e Celulose Company for allowing our access to the study areas; REBIO do Córrego Grande and FLONA do Rio Preto for providing accommodation and transportation to the study areas; and Conselho Nacional de Desenvolvimento Científico e Tecnológico – CNPq for funding
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