Woody encroachment threatens several ecosystems around the world. In general, management of grasslands includes regulation of fire and grazing regimes. Changes in these two types of disturbances are potential drivers of woody encroachment. Here we assessed how the traditional management carried out by local landholders affects a highland grassland ecosystem in southern Brazil. We hypothesized that grasslands converted to protected areas undergo fast woody encroachment. To reconstruct changes in vegetation, we interviewed former and current landholders and coupled their knowledge with an analysis of aerial and satellite images. During the first 11 years without fire and cattle, woody encroachment in grasslands increased exponentially. Woody encroachment occurred mostly by the replacement of grasslands by shrublands. Meanwhile, grasslands under traditional management remained almost unchanged for the last 40 years. The management of fire by local landholders has been part of their traditional practices for decades. Such management prevents large-scale wildfires and maintains natural highland grasslands. The quick pace of shrub encroachment in such grasslands threatens its exclusive diversity, human well-being and regional cultural heritage. Thus, conservation policies are needed to regulate and instruct about the use of fire as a management tool in highland grasslands of southern Brazil.
Extensive vegetation change can have important consequences in ecosystem functioning and economy1. For instance, woody encroachment (or woody plant encroachment), which is the increase in density, cover and biomass of shrubs or woody vegetation in grasslands2, has been reported around the world3. Woody encroachment is caused by several factors such as shifts in climate and biogeochemical cycles, changes in disturbance regimes (e.g. fire and grazing), or modification in ecological succession by introduction of non-native species or predator removal2,3,4,5. Woody encroachment alters fundamental ecological processes of ecosystems, including global carbon balances, reduction of water flow or groundwater recharge and the loss of biodiversity4,6,7. Because woody encroachment tends to negatively affect herbaceous vegetation, it constitutes a major threat to savanna and grassland ecosystems.
Control of woody encroachment is a key concern in rangelands. Woody encroachment reduces forage production, creates habitat for ectoparasites, and hampers animal handling4. Woody encroachment concerns land managers and methods for control and eradication include either fire, cutting trees, grazing, or a combination of these three methods8,9. Woody encroachment has been reported all over the world, e.g., southern Ethiopian savanna8, North American savanna, shrub‐steppe and grasslands ecosystems10, southeastern South American savanna11 (‘Campos’6), and Brazilian savanna (‘Cerrado’12). In highland grasslands of southern Brazil, extensive cattle grazing is part of the traditional management employed for centuries13. In addition, local ranchers control fire to promote sprouting of grassland vegetation and hinder forest expansion6,14. Fire use in the management of rangelands and protected areas is still controversial15,16, with an overlooking of fire and grazing by environmental agencies and protected area managers12. “Zero-fire” policies are adopted by several countries – including Brazil – to avoid and control fire in fire-prone ecosystems15. Despite some benefits of fire removal, such ecosystems face increasing risk of catastrophic fires because of the accumulation of flammable biomass. Catastrophic fires have detrimental effects on biodiversity17, human wellbeing and landscape cultural values14. When fire and grazing are prevented, tussock grasses and shrubs tend to replace small grasses and herbs16,18,19, leading unburned and ungrazed areas to changes in species richness and community composition16 and woody encroachment over time6,17,20. Although the fate of grasslands subjected to shrub encroachment might be difficult to predict21, shrub-encroached areas can either develop into forests (e.g.22) or remain in a stable shrubland state, where forest never develops23. Thus, the type of management used in rangelands can drive distinct vegetation dynamics.
High altitude grasslands ecosystems cover a wide geographical extent in southern Brazilian territory, delivering a huge number of benefits because of the ecosystem services they provide. Grasslands seem to be maintained by either fire or human activities, or both24 and are currently threatened by several factors, especially land use change16 and a weak set of conservation policies implemented by the Brazilian government6. In highlands, grasslands are interspersed with Araucaria forests (mixed rainforest)24, the latter being also threatened and reduced to ~12% of its original cover25. Mosaics containing Araucaria forests and highland grasslands integrate a domesticated landscape, which has been shaped by pre-Columbian societies via use and management of resources over millennia13,26. These societies contributed for a fast expansion of Araucaria forests since 1.5 ka BP. Furthermore, it is likely that pre-Columbian societies managed fire26,27, once it became frequent in that period28. Nowadays, fire is frequently used by local ranchers to promote grassland resprouting, which is beneficial for cattle grazing19. These activities (extensive cattle and burning) slow down natural forest expansion over grasslands6,29, contributing for the maintenance of high diversity in grasslands and across the landscapes14, sustaining ecosystem functions30.
We carried out a study in a highland grassland ecosystem in southern Brazil to assess which types of management local landholders use and the effects of their traditional management on subtropical highland grasslands. We hypothesize that vegetation dynamics is determined by the type of management. Specifically, grasslands are maintained by either fire or grazing, whereas protected areas should undergo woody encroachment because both types of disturbance are prevented. The encroachment of woody vegetation after traditional management abandonment is still poorly known to Brazilian highland grasslands (e.g.20), especially over different management types. Moreover, vegetation dynamics have never been evaluated between areas either with or without traditional management. We interviewed current and former landholders in order to understand which management practices they have been using in their lands. We then analyzed aerial photographs and satellite images to quantify vegetation changes. These two sources of information were used to check whether changes in vegetation depended on the type of management. We expected that traditional management would keep highlands grasslands by hindering woody encroachment, while areas without traditional management (no grazing and no fire) would allow for a fast woody encroachment.
We interviewed 36 landholders of 38 past or current rangelands. Five additional rangelands belonging to four more landholders were added because their property location and type of management were freely mentioned by our interviewees, especially by neighbors. Twenty-five properties have been managed with both cattle and fire, whereas 18 properties used to be managed in this way but are currently within the São Joaquim National Park (SJNP) protected area. Eleven rural properties were left out of our analysis because they did not meet our selection criteria, i.e., were located in areas with high geometric lens distortion (i.e. in the edges of aerial photographs – four properties), or had low grassland cover (less than 2 hectares – five properties), or no available image (two properties).
Together, all rangelands cover more than 12,000 ha (average ± standard deviation = 284.8 ± 341.6 ha) and are at ca 1500 m above sea level (1503.8 ± 146). The average time families own each property was 125.5 ± 78.5 years. Extensive cattle farming is the primary income, with an average density of 0.41 ± 0.13 animals ha−1. Fire was or is used by all landholders every ca 2 years (2 ± 0.5), in the end of the winter (August/September), to accelerate grassland regrowth for cattle. Lacking cattle and fire, 19.4% of landholders believe grasslands remain stable, 55.6% believe grasslands turn into shrublands, and 11.1% believe grasslands become forest over time. Table 1.
From 1978 images, 73 polygons were drawn in grasslands of selected rangelands, covering an area of 3,191 ha. The extent of grasslands within polygons was 3,118.1 ha in 1978, decreasing 12% (2,746.2 ha) in 2018. The average time rangelands were kept since abandonment of traditional management (thus converted to protected areas) was 8.4 ± 1.6 years.
Shrub encroachment accelerated with time since abandonment of traditional management (wAIC = 0.73), being very little affected by elevation. Table 2. The model containing only time since abandonment of traditional management explained 68% of variation in shrub encroachment. Figure 1. In areas where traditional management still consists of using fire and grazing cattle, shrub encroachment remained around 1% year−1. Conversely, areas which became protected, thus excluding cattle and fire, experienced changes increasing exponentially over time, with an average shrub encroachment of 4.8% year−1 (ranging from 0.03 to 9.1% year−1). The time needed to shrubs to encroach into 50 and 99% of grasslands was estimated in 12 and 30 years, respectively. Field expeditions confirmed that the main shrub species encroaching in areas without traditional management is the shrub Baccharis uncinella DC. (Asteraceae).
Changing land management had great impact in vegetation dynamics in our study system. Our results indicate that after cattle and fire withdrawal, grasslands underwent an exponential increase of shrub encroachment over time. Shrub encroachment proceeded in a fast pace in protected areas, replacing large extents of grasslands over short time. Following that pace, shrubs would entirely encroach over grasslands in ~30 years. Conversely, areas keeping traditional management faced little to no shrub encroachment over the last 40 years. These results corroborate our hypothesis and its consequences are discussed below.
Woody encroachment affects open-canopy ecosystems across the world, unleashing a need to understand its causes and consequences. Woody encroachment has been reported on African savannas1,8, North American savannas and grasslands10,31,32 and South American savannas and grasslands6,12,16, thus posing these ecosystems at risk. Several factors and their interactions cause woody encroachment, even though changes in disturbance regimes, such as fire and grazing, are amongst the most frequent drivers3,4,5,21. Therefore, the type of land management seems to be of paramount importance for landscape maintenance. For example, grasslands of subalpine ecosystems are being transformed into woodlands, facing shrub encroachment process as agricultural practices are abandoned33. In southern Brazil, grasslands converted into pine monocultures are vulnerable to shrub encroachment after pine removal, requiring active restoration16. In southeastern South America, the Uruguayan Savanna ecoregion faces a limited forest expansion because of cattle grazing and fire, although tree cover is favored by precipitation11. Our study supports the claim that highland grasslands in southern Brazil are prone to woody encroachment6,20, especially in the absence of fire and cattle grazing. Although substantial increases in woody encroachment can occur over decades4, we found evidence for an acceleration of shrub encroachment over time in areas where fire and cattle were excluded. Such management is normally enforced in protected grasslands (e.g.16,30,34). Meanwhile, native grasslands were maintained under traditional management by keeping large herbivores and fire. In North American drylands, for example, rates of encroachment vary from 0.1–2.3% year−1, depending on the ecoregion4,10. Here we found rates of shrub encroachment ranging from 0.03 to 9.1% year−1. In areas under traditional management, the average rate of shrub encroachment was 1.1% year−1, while in areas where traditional management was prevented the average rate was 4.8% year−1. Our results indicate a clear effect of the type of management on woody encroachment and highlights the fast pace it may follow.
Replacement of grasslands by woodlands has important consequences at both the community and ecosystem levels2,32. In general, chief consequences of woody encroachment are alteration of fundamental ecological processes and loss of biodiversity3,6,7,32. In addition, woody encroachment reduces the outcome of cattle production thus affecting human economies4,35. In the study region, all landholders have been using extensive cattle farming as their primary income for decades. In addition, all landholders manage fire to promote the regrowth of grasslands for cattle foraging in the end of the winter. Thus, it is not surprising that humans seem to shape ecosystems to reach their intended benefits. Over the last centuries, woody vegetation seems to be favored by the suppression of fire and grazing in subtropical ecosystems17 and the dependency of southern Brazilian highland grasslands on fire and grazing has been already reported (e.g.6,16,20,24,36,37,38). Fire and grazing are key elements of traditional management taken by local landholders in such system13,14. However, use and management of fire is still controversial6,15 and rarely described even in fire-managed pastoral systems12. Furthermore, Brazilian environmental agencies and protected area managers struggle to understand fire-managed pastoral systems12, which urges the creation of conservation policies that enable the use of fire in fire-prone ecosystems15. Fire brings benefits. For example, species richness of abandoned grasslands in southern Brazil can only be maintained by fire6. In Brazilian highland grasslands, fire and grazing exclusion can lead to decreases in species richness, changes in grassland physiognomy and species composition16, which can cause changes in ecosystem functioning30. In mesic grasslands of central United States, the prevention of woody encroachment by frequent burning is the best option32. In African moist and arid savannas, fire is an effective method for controlling shrub encroachment9. However, substantial ecosystem changes following woody encroachment may, in some cases, impair ecosystem recovery even when fire is reintroduced32. Also, fire must be used with responsibility, as in some cases it can favor invasive exotic species adapted to fire (e.g.39,40) or reach into forests when not adequately supervised or when the shrub component in the forest-grassland edge is too dense.
In general, few woody species tend to become aggressive encroachers or originate the encroachment process41. The main shrub species encroaching in the studied grasslands is Baccharis uncinella, which is a regionally common but endemic species to southern Brazilian highlands42. This species can expand from forest borders toward grasslands20 and facilitate the arrival and development of other shrubs and forest species, including nurse trees, potentially accelerating forest expansion22,43, as well as serving as a native fauna refugee36,38. A similar shrub-facilitation system has been reported in subalpine grasslands in Spain, in which a species of shrub that invaded grasslands facilitated the settlement and expansion of another shrub species33. We understand that a native shrubby vegetation, which seems to be a transient alternative state, can be beneficial at some level (see44) and deserves to be protected as well (see36,37,38). However, larger native grassland areas affected by woody encroachment as a result of fire and grazing suppression, can alter grassland communities, especially by reducing native forbs abundance and plant species richness45, as well as altering ecosystem functioning30. Besides, encroachment by B. uncinella seems to be facilitated by high air temperatures and native grasses23 and even monocultures16. At low to moderate densities, encroachment by B. uncinella seems to be easily controlled by fire. Under high density of B. uncinella, however, landscapes may be threatened by catastrophic fires.
Our findings show that highland grasslands that became protected by law – where both cattle grazing and fire are suppressed – faced woody encroachment. Conversely, highland grasslands under traditional management – with cattle grazing and fire – were maintained. Such management consists of 2-year fire interval, where different patches of grasslands are burned in each year, and low density of extensive grazing cattle (~0.41 animals ha−1). Most landholders we interviewed believe that, in the absence of cattle and fire, grasslands would turn into shrublands over time. Accumulation of flammable biomass, including that from B. uncinella encroachment, also concerns several of the landholders. In addition, landholders reported that unburned grasslands accumulate fuel and that shrubs facilitate fire spread to adjacent forests, because shrubs increase vertical reach of flames. Indeed, flammable biomass accumulates over time in grasslands areas where fire is prevented16,17,19 and shrubs, which are kept in low abundance in managed systems, establish and increase in abundance mostly from forest edges20. Once inside forests, fire can spread throughout the flammable litter of Araucaria trees. Araucaria is an abundant species and produces great part of the litter in Araucaria forests46. Also, litter in these forests have a lower decomposition rate compared to other forests (e.g., rainforests) because of the presence of oils and resin in Araucaria litter46, allowing fire to spread. Such characteristics may facilitate the occurrence of catastrophic fires, which impose a risk to biodiversity17, human wellbeing and cultural landscapes14. Natural grasslands, besides providing a more reliable carbon sink, can be more resilient to drought and wildfires than forests47,48. Therefore, policy makers and protected area managers should recognize fire as a natural and critical process in grasslands15, comprehend that degradation can affect protected grasslands30 and recognize that disturbances can be crucial to protect biodiversity-related and cultural aspects of the landscape.
We found additional evidence for woody encroachment by shrubs in grasslands from southern Brazil highlands. Yet, the most outstanding fact of our results is the pace of vegetation change exponentially accelerating during the first 11 years. Consequently, large extents of grasslands can be replaced by shrubs after just a decade of management change. In addition, we believe that local landholders (ranchers) understand consequences of their management – which includes fire and grazing by cattle – on both the maintenance of grasslands and the prevention of large-scale destructive wildfires. Based on such knowledge and vegetation change analysis, we suggest that the quick pace of shrub encroachment in the region threatens not only grassland ecosystems and its unique biodiversity, but also human wellbeing and cultural heritage of the landscape. Such results highlight the need of grassland conservation policies allowing and instructing on the timing, frequency and extent of prescribed fire regimes as a management tool for both rangelands and protected areas.
The study was conducted in the highlands of southern Brazil, in protected areas and rangelands in the São Joaquim National Park (SJNP) region, state of Santa Catarina, Brazil. Figure 2. This region encompasses one of the highest elevated zones of southern Brazil, reaching up to 1800 m a.s.l. The protected area has 49,300 ha, of which 13,000 ha have been acquired from former landholders by the Brazilian government since 2006. The main ecoregions in these highlands are high-altitude grasslands and mixed rainforest (Araucaria forest). The climate between 1961 and 2016, recorded at the nearest weather station (distant ca. 30 km), was characterized by an annual mean rainfall of 1,626.3 mm.yr−1, equally distributed throughout the year, and an annual mean temperature of 13.3 °C. The average minimum temperature for the coldest month (July) was 6.0 °C and the average maximum temperature for the hottest month (January) was 22.9 °C. The minimum absolute temperature recorded was −9.0 °C and the maximum absolute temperature was 31.4 °C. During winter, frosts are common, and snows are occasional. Climate data compiled from49.
In 2016 and 2017, we interviewed owners of existing rangelands and previous owners whose areas were acquired to join the SJNP. The participants were selected from a list of former and current landholders of the SJNP region provided by the SJNP manager. We tried to reach all landholders mentioned in the list. In addition to the provided list, we also employed snowball sampling to increase the number of participants. Before starting the interviews, we asked the participants whether they wanted or not to answer our questionnaire and a consent form with the study aims and legal consequences was delivered. This research followed the guidelines of the Ethics Committee from Federal University of Santa Catarina (CEPSH), which also approved the development of this research (CEPSH - 44039415.6.0000.0121; Number 1.095.964 of 08/06/2015). Statement on written informed consent has been obtained from all the participants. Questionnaires contained open-ended questions and followed a semi-structured guide. The questions aimed to get information on the property location and size, the residence and within-family ownership time, the type and frequency of management used in the area and their opinion on the fate of grasslands in the absence of cattle and fire. When cattle grazing was mentioned, we additionally asked how many animals they had. We asked the landholders to locate and delimit their current or past properties on a digital map. The authorization for developing this study in the protected area and private properties was approved by the Brazilian government (SISBio code 48898–1) and the landholders, respectively.
Acquisition and georeferencing. Aerial photographs taken in 1978 were acquired from a local public organ (Secretaria de Planejamento do Estado de Santa Catarina). These images have ~5490 × 5575 pixels (width × height) and 600 pixels inch−1 resolution. Very high-resolution satellite imagery (CNES’ Pleiades-1A data and Airbus’ SPOT series satellite data) taken in 2018 were acquired from Google Earth (GE - http://earth.google.com). Both 1978 and 2018 images were georeferenced in an orthorectified mosaic composed by aerial photographs from 2011 (Aerial Survey of the State of Santa Catarina – http://sigsc.sds.sc.gov.br). We used the Thin Plate Spline correction for both 1978 and 2018 images. The 2011 orthorectified mosaic was used as reference for ground control points (GCP). At least 20 GCP were established in each image, especially using roads, buildings and rocky outcrops as references. Figure 3.
Sampling procedure. We delimited polygons in which we quantified changes from past to current vegetation cover. Polygons were manually drawn for grasslands (on 1978 images) intersecting with past rangeland delimitation provided by interviewed landholders (Fig. 2). Forests were avoided whenever possible once our primary interest was to detect changes in grasslands and because preliminary inspection showed little changes in forest extent. Polygons were drawn at least 20 m away from buildings and from the edge of continuous forests, because such areas tend to rapidly change after traditional management abandonment20. We also placed polygons 20 m away from property limits, to avoid influence from neighbor areas for which we had no management information. Rangelands located in areas with high geometric lens distortion (i.e. in the edges of aerial photographs), with low grassland cover (i.e. less than 2 hectares) or with no available image, were discarded from the analysis.
Classification. We carried out a supervised classification using maximum likelihood algorithm. Because polygons were drawn for 1978 images, when traditional management was in place (data acquired from interviews), such images were classified in two classes: grassland and forest. In turn, 2018 images were classified in the following classes: grassland, shrubland, water bodies, rocky outcrops, plantations and buildings. Figure 3. Classification accuracy was assessed via Cohen’s coefficient (κ). We only accepted classifications when κ > 0.8, indicating an overall good performance50. Then, the area occupied by each class was calculated for each polygon. Finally, classes only observed in 2018 images (e.g. rock outcrops, water bodies, buildings and plantations) were discarded from the total polygon area in both times. We validated the classification outcome by field expeditions. Image classification was carried out in MultiSpec software, version 3.451 (https://engineering.purdue.edu/~biehl/MultiSpec/). QGis platform version 2.18.2052 was used for georeferencing, mosaic building and area measurements.
Because polygons varied in size depending on property settings, we obtained the proportional extent of every class over the whole polygon extent. We used beta regression models (with a logit link function) to model shrub encroachment, i.e. the increase in shrub area (%) from 1978 to 2018. Beta regression models are suitable to model proportions, because the beta distribution assumes values in the interval (0, 1)53. As predictors of shrub encroachment, we used the time since abandonment of traditional management (in years) and elevation. The interaction between both predictors was also tested, because we expected upper areas could change at a slower pace than lower ones within the same time extent. Model selection was based on the Akaike information criterion corrected for small sample sizes (AICc)54 and validated by a graphical analysis of residuals. We constructed 95% confidence intervals for the predicted values based on 1000 bootstrap samples from the original data55. All analyses were carried out in the R environment56. Package “betareg”53 was used for model building and predictions and “ggplot2”57 for visualization of model outputs.
All data generated during this study are included in this published article (Table 1 – Results section).
Venter, Z. S., Cramer, M. D. & Hawkins, H. J. Drivers of woody plant encroachment over Africa. Nat. Commun. 9, 1–7 (2018).
Van Auken, O. W. Shrub Invasions of North American Semiarid Grasslands. Annu. Rev. Ecol. Syst. 31, 197–215 (2000).
Eldridge, D. J. et al. Impacts of shrub encroachment on ecosystem structure and functioning: Towards a global synthesis. Ecol. Lett. 14, 709–722 (2011).
Archer, S. R. et al. Woody plant encroachment: causes and consequences. In Rangeland systems 25–84 (Springer, 2017).
Van Auken, O. W. Causes and consequences of woody plant encroachment into western North American grasslands. J. Environ. Manage. 90, 2931–2942 (2009).
Overbeck, G. E. et al. Brazil’s neglected biome: The South Brazilian Campos. Perspect. Plant Ecol. Evol. Syst. 9, 101–116 (2007).
Scholes, R. J. & Archer, S. R. Tree-Grass Interactions in Savannas. Annu. Rev. Ecol. Syst. 28, 517–544 (1997).
Angassa, A., Resources, N., Tolera, A. & Oba, G. Bush encroachment control demonstrations in southern Ethiopia: 1. Woody species survival strategies with implications for herder land management. Afr. J. Ecol. 47, 63–76 (2009).
Trollope, W. S. W. Controlling bush encroachment with fire in the savanna areas of South Africa. Proc. Annu. Congr. Grassl. Soc. South. Africa 15, 173–177 (1980).
Barger, N. N. et al. Woody plant proliferation in North American drylands: A synthesis of impacts on ecosystem carbon balance. J. Geophys. Res. Biogeosciences 116, 1–17 (2011).
Bernardi, R. E., Holmgren, M., Arim, M. & Scheffer, M. Why are forests so scarce in subtropical South America? The shaping roles of climate, fire and livestock. For. Ecol. Manage. 363, 212–217 (2016).
Eloy, L., Schmidt, I. B., Borges, S. L., Ferreira, M. C. & dos Santos, T. A. Seasonal fire management by traditional cattle ranchers prevents the spread of wildfire in the Brazilian Cerrado. Ambio, https://doi.org/10.1007/s13280-018-1118-8 (2018).
Reis, M., Ladio, A. & Peroni, N. Landscapes with Araucaria in South America: evidence for a cultural dimension. Ecol. Soc. 19, (2014).
Sühs, R. B., Giehl, E. L. G. & Peroni, N. Interaction of land management and araucaria trees in the maintenance of landscape diversity in the highlands of southern Brazil. PLoS One 13 (2018).
Mistry, J., Schmidt, I. B., Eloy, L. & Bilbao, B. New perspectives in fire management in South American savannas: The importance of intercultural governance. Ambio 1–8, https://doi.org/10.1007/s13280-018-1054-7 (2018).
Andrade, B. O., Bonilha, C. L., Ferreira, P. M. A., Boldrini, I. I. & Overbeck, G. E. Highland grasslands at the southern tip of the atlantic forest biome: Management options and conservation challenges. Oecologia Aust. 20, 37–61 (2016).
Behling, H. & Pillar, V. D. Late Quaternary vegetation, biodiversity and fire dynamics on the southern Brazilian highland and their implication for conservation and management of modern Araucaria forest and grassland ecosystems. Philos. Trans. R. Soc. B Biol. Sci. 362, 243–251 (2007).
Boldrini, I. I. & Eggers, L. Vegetação campestre do sul do Brasil: dinâmica de espécies à exclusão do gado. Acta Bot. Brasilica 10, 37–50 (1996).
Nabinger, C., Moraes, A. de & Maraschin, G. E. Campos in southern Brazil. in Grassland ecophysiology and grazing ecology (eds. Lemaire, G., Hodgson, J., Moraes, A. de, Nabinger, C. & Carvalho, P. C. de F.) 355–376, https://doi.org/10.1079/9780851994529.0355 (CABI, 2000).
Oliveira, J. M. & Pillar, V. D. Vegetation dynamics on mosaics of Campos and Araucaria forest between 1974 and 1999 in Southern Brazil. Community Ecol. 5, 197–202 (2004).
Auken, V. O. W. Shrub invasions of North American semiarid grassland. Annu. Rev. Ecol. Syst. 31, 197–215 (2000).
Duarte, L. D. S., Dos-Santos, M. M. G., Hartz, S. M. & Pillar, V. D. Role of nurse plants in Araucaria Forest expansion over grassland in south Brazil. Austral Ecol. 31, 520–528 (2006).
Dechoum, M. S., Peroni, N. & Pugnaire, F. I. Factors controlling shrub encroachment in subtropical montane systems. Appl. Veg. Sci. 21, 190–197 (2018).
Klein, R. M. Aspectos dinâmicos da vegetação do sul do Brasil. Sellowia 36, 5–54 (1984).
Ribeiro, M. C., Metzger, J. P., Martensen, A. C., Ponzoni, F. J. & Hirota, M. M. The Brazilian Atlantic Forest: How much is left, and how is the remaining forest distributed? Implications for conservation. Biol. Conserv. 142, 1141–1153 (2009).
Bitencourt, A. L. V. & Krauspenhar, P. M. Possible prehistoric anthropogenic effect on Araucaria angustifolia (Bert.) O. Kuntze expansion during the late Holocene. Rev. Bras. Paleontol. 9, 109–116 (2006).
Kern, A. A. Antecedentes indígenas: problemáticas teórico-metodológicas das sínteses sobre a pré-história regional. Rev. do Mus. Arqueol. e Etnol. 15–24 (1998).
Behling, H., Pillar, V. D., Orloic, L. & Bauermann, S. G. Late Quaternary Araucaria forest, grassland (Campos),fire and climate dynamics, studied by high-resolution pollen, charcoal and multivariate analysis of the Cambara do Sul core in southern Brazil. Palaeogeogr. Palaeoclimatol. Palaeoecol. 203, 277–297 (2004).
Pillar, V. D. P. Dinâmica da expansão florestal em mosaicos de floresta e campos no Sul do Brasil. in Ecossistemas Brasileiros: Manejo e Conservação (ed. Claudino-Sales, V.) 209–216 (Expressão Gráfica, Fortaleza, 2003).
Leidinger, J. L. G. et al. Historical and recent land use affects ecosystem functions in subtropical grasslands in Brazil. Ecosphere 8, (2017).
Knapp, A. K. et al. Shrub encroachment in North American grasslands: Shifts in growth form dominance rapidly alters control of ecosystem carbon inputs. Glob. Chang. Biol. 14, 615–623 (2008).
Lett, M. S. & Knapp, A. K. Consequences of shrub expansion in mesic grassland: Resource alterations and graminoid responses. J. Veg. Sci. 14, 487–496 (2003).
Nuche, P. & Alados, C. L. Shrub interactions drive vegetation succession of subalpine grasslands under two climatic conditions. J. Plant Ecol. 11, 297–307 (2018).
Oliveira, J. M. & Pillar, V. D. Vegetation dynamics on mosaics of Camposand Araucaria forest between 1974 and 1999 in Southern Brazil. Community Ecol. 5, 197–202 (2004).
Oba, G., Post, E., Syvertsen, P. O. & Stenseth, N. C. Bush cover and range condition assessments in relation to landscape and grazing in southern Ethiopia. Landsc. Ecol. 15, 535–546 (2000).
Carlucci, M. B., Luza, A. L., Hartz, S. M. & Duarte, L. D. S. Forests, shrublands and grasslands in southern Brazil are neglected and have specific needs for their conservation. Reply to Overbeck et al. Nat. e Conserv. 14, 155–157 (2016).
Luza, A. L., Carlucci, M. B., Hartz, S. M. & Duarte, L. D. S. Moving from forest vs. grassland perspectives to an integrated view towards the conservation of forest–grassland mosaics. Nat. Conserv. 12, 166–169 (2014).
Overbeck, G. E., Ferreira, P. M. A. & Pillar, V. D. Conservation of mosaics calls for a perspective that considers all types of mosaic-patches. Reply to Luza et al. Nat. Conserv. 14, 152–154 (2016).
Keeley, J. E. Fire Management Impacts on Invasive Plants in the Western United States. Conserv. Biol. 20, 375–384 (2006).
Grace, J. B., Smith, M. D., Grace, S. L., Collins, S. L. & Stohlgren, T. J. Interactions between fire and invasive plants in temperate grasslands of North America. In Proceedings of the invasive species workshop: the role of fire in the control and spread of invasive species. Fire conference 40–65 (2000).
Stokes, C. J. & Archer, S. R. Niche differentiation and neutral theory: An integrated perspective on shrub assemblages in a parkland savanna. Ecology 91, 1152–1162 (2010).
Heiden, G. & Schneider, A. Baccharis in Lista de Espécies da Flora do Brasil. Rodriguésia 66, 1085–1113 (2015).
dos Santos, M. M. G., Oliveira, J. M., Müller, S. C. & Pillar, V. D. Seed rain of woody species in mosaics of Araucaria forest and grasslands in Southern Brazil. Acta Bot. Brasilica 25, 160–167 (2011).
Maestre, F. T., Eldridge, D. J. & Soliveres, S. A multifaceted view on the impacts of shrub encroachment. Appl. Veg. Sci. 19, 369–370 (2016).
Guido, A., Salengue, E. & Dresseno, A. Effect of shrub encroachment on vegetation communities in Brazilian forest-grassland mosaics. Perspect. Ecol. Conserv. 15, 52–55 (2017).
Backes, A., Prates, F. L. & Viola, M. G. Produção de serapilheira em Floresta Ombrófila Mista, em São Francisco de Paula, Rio Grande do Sul, Brasil. Acta Bot. Brasilica 19, 155–160 (2005).
Pawlok, D., Benjamin, Z. H., Yingping, W. & David, W. Grasslands may be more reliable carbon sinks than forests in California. Environ. Res. Lett. 13, 74027 (2018).
Seddon, N., Turner, B., Berry, P., Chausson, A. & Girardin, C. A. J. Grounding nature-based climate solutions in sound biodiversity science. Nat. Clim. Chang. 9, 84–87 (2019).
INMET - Instituto Nacional de Meteorologia. Available at: http://www.inmet.gov.br/portal/index.php?r=clima/normaisClimatologicas. (Accessed: 10th August 2017)
Fleiss, J. L. Statistical Methods for Rates and Proportions (2nd ed.). John Wiley Sons 800 (1981).
Biehl, L. & Landgrebe, D. MultiSpec- a tool for multispectral-hyperspectral image data analysis. Comput. Geosci. 28, 1153–1159 (2002).
QGIS. QGIS Geographic Information System. Open Source Geospatial Foundation Project, http://www.qgis.org/ (2017).
Cribari-Neto, F. & Zeileis, A. Beta Regression in R Beta Regression in R. Research Report Series/Department of Statistics and Mathematics 98, (2009).
Zuur, A. F., Ieno, E. N., Walker, N., Saveliev, A. A. & Smith, G. M. Mixed effects models and extensions in ecology with R. Mixed effects models and extensions in ecology with R, https://doi.org/10.1007/978-0-387-87458-6 (2009).
Ospina, R., Cribari-Neto, F. & Vasconcellos, K. L. P. Improved point and interval estimation for a beta regression model. Comput. Stat. Data Anal. 51, 960–981 (2006).
R Core team. R Core Team. R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria. ISBN 3-900051-07-0, http://www.R-project.org/ 55, 275–286 (2015).
Wickham, H. ggplot2: Elegant Graphics for Data Analysis. (Springer-Verlag New York, 2016).
We thank Dr. Emanuela Weidlich, Dr. Michele Dechoum, Dr. Marcos Carlucci, Dr. Pedro Higuchi and MSc. Alexandre M.S. Machado for manuscript suggestions; Dr. Juliano Bogoni for assisting with the interviews; MSc. Michel Omena and SJNP staff for logistical support and properties’ data provision, Mr. Eriovan Matias for sharing his knowledge and experiences and all the interviewees for their contribution.
The authors declare no competing interests.
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Sühs, R.B., Giehl, E.L.H. & Peroni, N. Preventing traditional management can cause grassland loss within 30 years in southern Brazil. Sci Rep 10, 783 (2020). https://doi.org/10.1038/s41598-020-57564-z
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