- Open Access
Improving the knowledge of plant potential biodiversity-ecosystem services links using maps at the regional level in Southern Patagonia
Ecological Processes volume 10, Article number: 53 (2021)
Biodiversity supports multiple ecosystem services, whereas species loss endangers the provision of many services and affects ecosystem resilience and resistance capacity. The increase of remote sensing techniques allows to estimate biodiversity and ecosystem services supply at the landscape level in areas with low available data (e.g. Southern Patagonia). This paper evaluates the potential biodiversity and how it links with ecosystem services, based on vascular plant species across eight ecological areas. We also evaluated the habitat plant requirements and their relation with natural gradients. A total of 977 plots were used to develop habitat suitability maps based on an environmental niche factor analysis of 15 more important indicator species for each ecological area (n = 53 species) using 40 explanatory variables. Finally, these maps were combined into a single potential biodiversity map, which was linked with environmental variables and ecosystem services supply. For comparisons, data were extracted and compared through analyses of variance.
The plant habitat requirements varied greatly among the different ecological areas, and it was possible to define groups according to its specialization and marginality indexes. The potential biodiversity map allowed us to detect coldspots in the western mountains and hotspots in southern and eastern areas. Higher biodiversity was associated to higher temperatures and normalized difference vegetation index, while lower biodiversity was related to elevation and rainfall. Potential biodiversity was closely associated with supporting and provisioning ecosystem services in shrublands and grasslands in the humid steppe, while the lowest values were related to cultural ecosystem services in Nothofagus forests.
The present study showed that plant species present remarkable differences in spatial distributions and ecological requirements, being a useful proxy for potential biodiversity modelling. Potential biodiversity values change across ecological areas allowing to identify hotspots and coldspots, a useful tool for landscape management and conservation strategies. In addition, links with ecosystem services detect potential synergies and trade-offs, where areas with the lowest potential biodiversity are related to cultural ecosystem services (e.g. aesthetic values) and areas with the greatest potential biodiversity showed threats related to productive activities (e.g. livestock).
Biodiversity is critical to support multiple ecosystem services (ES) (MEA 2005; Cardinale 2012; Mace et al. 2012). Several studies agree that plant biodiversity strongly affects supporting and regulating ES, e.g. soil nutrients cycling, productivity, and erosion control (Chen et al. 2018; Peri et al. 2019a; Ma et al. 2020). Furthermore, plant communities provide essential habitats for a wide range of species (Wen et al. 2020). Traditional management only focused on few provisioning ES, which is one of the main threats to biodiversity (Kohler et al. 2017). As a consequence, biodiversity loss endangers the provision of many other ES (MAES 2013; Shih 2020), affecting ecosystem resilience and resistance capacity to face climate change or species invasions (Kohler et al. 2017; Pires et al. 2018). Nevertheless, understanding these complex interactions represent a challenge, due to the multiple roles that biodiversity plays in the delivery of ES (MAES 2013; Mori et al. 2017).
Different factors affect species diversity distribution, where environmental heterogeneity (e.g. climate, soil, and topography) is the main driver for landscape variation in species composition across different taxa and biomes (Stein et al. 2014; Li et al. 2020). In consequence, plant biodiversity changes according to the different ecosystem types, e.g. temperate forests present unique understory species associated with tree canopy structure and composition (Barbier et al. 2008; Lencinas et al. 2008), while grasslands present characteristic species associated with temperature and rainfall gradients (Peri et al. 2016a; Li et al. 2020). In addition, soil characteristics as stock carbon and water balance, and topography as elevation and slope, influence plant distribution, richness, and diversity (e.g. Dubuis et al. 2013; Pottier et al. 2013; Peri et al. 2019a; Jordan et al. 2020). However, it is not totally understood how plant species distribution is linked with regional environmental variables (Kreft and Jetz 2007; Xu et al. 2016; Martínez Pastur et al. 2016a) and how biodiversity is related to ES supply (Schneiders et al. 2012; Martínez Pastur et al. 2017). Remote sensing techniques became a powerful tool for qualitative and quantitative modelling of plant species distribution and habitat prediction at the landscape level (Wiersma et al. 2011). One of the most employed methods is based on the combination of field plots with satellite data (Dubuis et al. 2013; Pottier et al. 2013), where the Biomapper software showed its advantage to the development of potential habitability suitability (PHS) models (Hirzel et al. 2001, 2006) in areas with scarce data as Southern Patagonia (Rosas et al. 2017). These models relate regional environmental characteristics (e.g. climatic, topographic, landscape) with the occurrence of species in one particular area (Guisan and Zimmermann 2000; Hirzel et al. 2002) determining the PHS of each species. During the last years, studies in plant species distribution were significantly increased (Bradley et al. 2012), mostly related to woody species (Silva et al. 2017), and invasive (Chai et al. 2016; Wan and Wang 2018) or endangered plant species (Abdelaal et al. 2020). Nevertheless, few studies combined multiple PHS to create a unique potential biodiversity map (PBM) that synthetizes the information for multiple species at the landscape level (e.g. Martínez Pastur et al. 2016a; Rosas et al. 2019a). PHS maps allow to understand the ecology of ecosystem communities (Martínez Pastur et al. 2016a), recognize environmental predictors of species distribution (Dubuis et al. 2013; Pottier et al. 2013), identify potential hotspots of biodiversity (Wulff et al. 2013), and analyse the natural protected area network effectiveness and representativeness (Rosas et al. 2019a). However, few studies have linked the biodiversity and the ES supply to understand their relationship and support landscape management and conservation planning (Martínez Pastur et al. 2017; Shih 2020).
Southern Patagonia, specifically Santa Cruz Province, has a well-conserved wilderness landscape with a unique ecosystem variety, where temperature and rainfall patterns strongly defined the natural vegetation types. The region can be classified into eight main ecological areas, where dry steppes dominate in the northeast (central plateau, shrub-steppe of San Jorge Gulf, and mountains and plateaus), and shrublands and humid steppes (humid and dry Magellanic grass steppe) prevail in the southeast, while sub-Andean grasslands, Nothofagus forests, and alpine vegetation occupy a narrow strip in the west (Oliva et al. 2004) (Fig. 1). The vegetation types influence the provisioning ES delivery, generating several trade-offs between biodiversity and other ES supplies (Peri et al. 2016a, 2018, 2019b). Traditionally, steppe and shrubland areas present provisioning ES related to livestock production, where different management proposals have been implemented (Peri et al. 2016b). Peri et al. (2013) also showed that different grazing strategies influence plant communities at the landscape level, where intensive management using mechanical shredding to remove shrubs significantly modified the arthropod community (Sola et al. 2016). Besides, extreme climatic conditions and overgrazing in dry steppes determined the highest values of desertification (Del Valle et al. 1998; Peri et al. 2016b; Gaitán et al. 2019). Recently, it was possible to map cultural ES (Martínez Pastur et al. 2016b), where higher values were related to cities close to protected areas and touristic routes (Rosas et al. 2019b). Forestry was conducted in the forests close to Los Andes; N. antarctica forests are related to livestock grazing in private lands (Peri et al. 2016c), while N. pumilio and evergreen forests are mainly under protected areas (Peri et al. 2019c). These studies also determined the impact of forest management alternatives on N. antarctica forests, where some multi-objective strategies (e.g. silvopastoral systems) allowed to maintain biodiversity values and increase ES delivery on time.
Regional plant diversity studies stand out for defining dominant vegetation types (Oliva et al. 2004; Oyarzabal et al. 2018) at the coarse resolution level and were used to identify potential negative trade-offs with different management activities at the local scales (Peri et al. 2016a, 2016b, 2016c). The efforts to increase landscape ecology studies represent a challenge in remote areas such as Santa Cruz Province, where available data is scarce. Biodiversity mapping was studied through endangered species (Rosas et al. 2017), as well as lizards and darkling beetles (Rosas et al. 2018, 2019c), which represent good proxies for specific vegetation types. Martínez Pastur et al. (2016a) proposed understory plants as proxies of potential biodiversity in Tierra del Fuego forests, because they have a wider distribution than other taxonomic groups, and Rosas et al. (2019a) also apply this methodology for Santa Cruz forests. However, these efforts for mapping biodiversity are not enough to compare the different vegetation types at the regional level, e.g. lizards and darkling beetles occurred in arid environments and not in forests. To understand the role that biodiversity plays in the ES delivery (MAES 2013), it is necessary to link biodiversity and ES supply at the landscape level, using the same proxy taxonomic group. With one unique map, it will be possible to analyse the potential trade-offs with other ES deliveries at the regional level (e.g. Martínez Pastur et al. 2017). In this context, the objective was to evaluate the potential biodiversity of the entire Santa Cruz Province (Argentina) and their linking with ES delivery, based on vascular plant species distribution as a proxy along the different ecological areas of the region. We also define the following specific objectives: (i) determine how much variation presents the habitat for indicator plants across the different ecological areas, (ii) relate PBM and environmental variables, and (iii) link PBM and ES supply. We hypothesized that (i) the distribution of the species is related to environmental gradients (Riesch et al. 2018), which together with other factors (e.g. biotic factors such as predation risk) define the potential biodiversity of one particular ecosystem; (ii) the provision of the different ES is not independent, interaction among them according to the species assemblage and biophysical characteristics of the ecosystems (Martínez Pastur et al. 2016a; Martínez Pastur et al. 2017); and (iii) human pressures on natural ecosystems due to economic activities (e.g. livestock use, silvopastoral management, forestry) generates synergies and trade-offs between provisioning ES and the other ES and biodiversity conservation (e.g. Peri et al. 2016b; Martínez Pastur et al. 2017). We expect to bring some evidences about these links between ES and biodiversity and provide tools for managers and decision-makers to propose more effective conservation alternatives at the regional level.
The study area includes Santa Cruz Province (Argentina) between 46° 00′ and 52° 30′ S, and between 66° 00′ and 73° 00′ W (Fig. 1a). The annual temperature increases from south to north (6.1 to 9.6 °C, Fig. 1b) with a mean annual range from − 2.6 to 19.5 °C (coldest and warmest months), while precipitation increases from east to west (204.1 to 899.7 mm year−1, Fig. 1c) with a mean annual range from 13.7 to 30.3 mm month−1 (driest and wettest months). This environmental pattern strongly influences the normalized difference vegetation index (NDVI), where the highest values were detected in the west, medium values in the south, and lowest values in the northeast (Fig. 1d). As was described before, the province was classified in different ecological areas considering soil qualities, regional climate, and the dominant plant communities (modified from Oliva et al. 2004) (Fig. 1e): (i) Dry steppes (DS) are located in the north including central plateau steppes (CP), shrub-steppe San Jorge Gulf (SSJG), and steppes in mountains and plateaus (MP), covering an area of 156,764 km2. This area presents the lowest vegetation cover, mainly associated with small shrubs (e.g. Nassauvia glomerulosa) and grasses (e.g. Stipa spp.). (ii) Shrublands (SL) cover 28,373 km2 and are dominated by Mulguraea tridens. (iii) Humid steppes (HS) are divided into humid and dry Magellanic grass steppes (HMGS and DMGS, respectively), covering an area of 17,831 km2, and are composed mainly by grasses (e.g. Festuca spp. and Carex spp.) in the south. Finally, other two ecological areas are located near to the Andes Mountains in the west, (iv) sub-Andean grasslands (SAG) that cover 8473 km2 and are dominated by Festuca pallescens and (v) Nothofagus forests and alpine vegetation (FAV) that cover 6658 km2.
A total of 53 plant species were selected for PHS modelling (Appendix 1). We used 977 plot surveys, where 235 plots belong to the PEBANPA network (Parcelas de Ecología y Biodiversidad de Ambientes Naturales en Patagonia Austral) (Peri et al. 2016a), and 742 plots belong to FAMA laboratory (Forestal, Agrícola y Manejo del Agua of INTA EEA-Santa Cruz). This database includes vascular plant species, bare soil, and inferior plants (e.g. bryophytes and lichens) based on cover (%) and frequency of occurrence (%). We calculated a cover-occurrence index selecting the 15 most important plant species for each ecological area. Each species must present at least 20 presence points following the methodology described in Rosas et al. (2019a). Then, the database was complemented with the available data for the selected species in the Sistema Nacional de Datos Biológicos of Ministerio de Ciencia, Tecnología e Innovación Productiva (www.datosbiologicos.mincyt.gob.ar) (final presence points = 5914). Additionally, we explored 40 potential explanatory variables, which were rasterized at 90 × 90 m resolution using the nearest resampling technique on the ArcMap 10.0 software (ESRI 2011), where all variables (climate, topography, landscape) used in this study were previously described in Rosas et al. (2017, 2018).
Potential biodiversity was analysed considering the occurrence across the landscape and their links with the ES type supply through the comparison of the selected environmental variables in the PHS modelling (Appendix 2) and the main ecological areas. In addition, to link PBM values with ES supply (CICES V5.1, Haines-Young and Potschin 2018) we used different proxies to discuss potential trade-offs, according to available maps (grids) for the study area: (i) Supporting and regulating ES were related to soil quality and carbon sequestration through soil organic carbon and nitrogen (Peri et al. 2018, 2019b), annual net primary productivity (Zhao and Running 2010), and desertification index (Del Valle et al. 1998) as a reverse proxy of soil control erosion. Soil organic carbon and nitrogen, as well desertification index, were modelled by related field data with climate and topographic variables. Annual net primary productivity was modelled using global productivity data of different ecosystems and remote sensing. (ii) Provisioning ES were related to food production through the probability of sheep occurrence (Pedrana et al. 2010), which were modelled according to climate and other bio-physical variables. Finally, (iii) cultural ES were related to spiritual, symbolic, and other interactions with the natural environment including aesthetic, existence, local identity, and recreational values (Martínez Pastur et al. 2016b; Rosas et al. 2019b). The cultural ES (aesthetic value, existence value, recreation, and local identity) were mapped using geo-tagged digital images that local people and visitors posted on web platforms, which were related to social and biophysical landscape features.
Models and statistical analyses
For modelling, we follow previous regional proposals for forests in Tierra del Fuego (Martínez Pastur et al. 2016a) and Santa Cruz (Rosas et al. 2019a) and methodological analyses of trade-offs to compare biodiversity and ES (Martínez Pastur et al. 2017) (see the chart flow presented in Fig. 2). PHS models for each plant species were based on the environmental niche factor analysis (ENFA) (Hirzel et al. 2002) using the Biomapper 4.0 software (Hirzel et al. 2004). ENFA employed the concept of ecological niche (Hutchinson 1957), comparing the eco-geographical variable distribution of presence dataset (locations of plant species) with the predictor distribution for the whole study area (Hirzel et al. 2001). ENFA summarizes all predictor variables and calculates two specific ecological relevance indexes: (i) Marginality (0 to 1) describes how far the optimum species habitat is from the mean environmental conditions of the study area, where higher values indicate that species grow in extreme environmental conditions. And (ii) global tolerance or specialization (tolerance−1) varied from 0 to infinite and describes the narrowness of the species niche, where higher values indicate that species tend to live in a narrow range of environmental conditions (Hirzel et al. 2002; Martínez Pastur et al. 2016a). We used a distance of geometric-mean algorithm to perform each PHS, which provides a good generalization of the niche (Hirzel and Arlettaz 2003). Each ENFA model results in a continuous PHS map with a range from 0 (minimum) to 100 (maximum habitat suitability). We used only the presence data in order to assess the statistical fit of each PHS model. ENFA used a cross-validation (Hirzel et al. 2006), evaluating the robustness and the predictive power of the models through Boyce index (B), continuous Boyce index (Bcont), proportion of validation points (P), absolute validation index (AVI), and contrast validation index (CVI) (Boyce et al. 2002; Hirzel and Arlettaz 2003; Hirzel et al. 2004, 2006). All these indices were described in Rosas et al. (2017, 2018).
We visualized PHS maps for each species into a geographical information system (GIS) with a resolution of 90 × 90 m, and we combined them with a mask based on NDVI < 0.05 to detect bare soil, ice fields, and water bodies (Lillesand and Kiefer 2000). Then, the 53 PHS maps were combined (average values for each pixel) to obtain the final PBM. This map had scores that varied from 1 to 46% (average values of PHS for all the studied species), and it was re-scaled by a lineal method from 0 to 100%. PBM was analysed using one-way ANOVAs. For this, we extracted the data from PBM using the hexagonal binning processes (each hexagonal = 250,000 ha) and calculated the average of potential biodiversity (PB) for each hexagon. After that, we classified each hexagon according to its PB values: (i) low was < 51% (32 hexagons), (ii) medium was 52–62% (44 hexagons), and (iii) high was > 63% (41 hexagons). The thresholds for each category were defined considering an equal number of pixels in the PBM. Finally, we analysed the extracted PB values considering the variables employed in the modelling, the main ecological areas, and ES proxies for each hexagon.
Potential habitat suitability of vascular plant species
The selected relevant indicator plant species belong to twenty-one different families (Appendix 1), mainly Poaceae (n = 18), Asteraceae (n = 9), and Cyperaceae (n = 4). Other families presented two different species, as Apiaceae, Berberidaceae, Ericaceae, and Rosaceae (n = 8), while other families only were represented by one species (Blechnaceae, Calceolariaceae, Caryophyllaceae, Ephedraceae, Escalloniaceae, Fabaceae, Lamiaceae, Plumbaginaceae, Polemoniaceae, Ranunculaceae, Rubiaceae, Solanaceae, Verberaceae, Violaceae) (n = 14).
The species with the highest presence points was Osmorhiza chilensis (n = 357), while the lowest was Poa ligularis (n = 21) (Table 1). Three species presented a wide distribution and were related to six different ecological areas, e.g. Festuca pallescens was the most important species in SAG (frequency = 60%), P. spiciformis was the second important species in SL (frequency = 72%), and Pappostipa chrysophylla was the third important species in CP and MP (frequency = 61 and 60%, respectively). Another three species were related to five different ecological areas, e.g. Berberis microphylla was the second important species in SAG (frequency = 50%), while Carex andina was the second (frequency = 88%) and Nardophyllum bryoides was the third important species (frequency = 63%) in DMGS. Four species were related to four ecological areas, e.g. Festuca gracillima was the most important species in DMGS (frequency = 81%), as well as Nassauvia glomerulosa in CP (frequency = 72%) and N. ulicina in SSJG (frequency = 62%), and Senecio filaginoides was the third important species in SAG (frequency = 54%). Eight species (Acaena poeppigiana, Avenella flexuosa, Bromus setifolius, Carex argentina, Empetrum rubrum, Mulguraea tridens, Pappostipa ibarii, P. sorianoi) were related to three ecological areas, e.g. four presented high-ranking values (up to third): Avenella flexuosa was the most important species in HMGS (frequency = 59%), as well as Mulguraea tridens in SL (frequency = 52%) and Pappostipa sorianoi in MP (frequency = 70%), while Empetrum rubrum was the second important species in FAV (frequency = 33%). Twelve species (Acaena magellanica, Azorella prolifera, Chiliotrichum diffusum, Chuquiraga aurea, Clinopodium darwinii, Festuca magellanica, Galium aparine, Gaultheria mucronata, Hordeum comosum, Osmorhiza chilensis, Pappostipa chubutensis, Rytidosperma virescens) were related to two ecological areas, e.g. O. chilensis presented high-ranking value in FAV (frequency = 48%) and Ch. diffusum the third important species in HMGS (frequency = 27%). Finally, twenty-three species (Adesmia volckmannii, Agrostis capillaris, A. perennans, Anemone multifida, Armeria maritima, Baccharis magellanica, Berberis empetrifolia, Blechnum penna-marina, Calceolaria uniflora, Carex macloviana, Chuquiraga avellanedae, Colobanthus subulatus, Ephedra chilensis, Escallonia rubra, Festuca argentina, Hordeum pubiflorum, Juncus balticus, Lycium chilense, Microsteris gracilis, Perezia recurvata, Poa lanuginosa, P. ligularis, Viola magellanica) were related to only one ecological area, where only Chuquiraga avellanedae presented the highest-ranking value in SSJG (frequency = 67%).
In the modelling of PHS maps, nine variables were the most appropriate to include in the analyses due to lower correlation values among all variables, and where only four variables presented higher values (> 0.80) based on Pearson’s correlation index (Appendixes 3 and 4). The most useful variables in the 53 PHS-adjusted maps were annual mean temperature (AMT), annual precipitation (AP), and normalized difference vegetation index (NDVI). The correlation index among the nine selected variables varied between 0.03 and 1.00. The lowest correlation was detected between the minimum temperature of the coldest month (MINCM) and the distance to rivers (DR) (0.03), and the highest was between the maximum temperature of the warmest month (MAXWM) and the global potential evapotranspiration (EVTP) (1.00), AMT and MAXWM (0.98), AMT and EVTP (0.96), and MINCM and elevation (ELE) (− 0.85).
The outputs of the 53 PHS models explained 100% of the information in the first four axes. Ephedra chilensis, Nassauvia ulicina, and Senecio filaginoides explained 95% of the information in the first axis, while Viola magellanica, Chuquiraga avellanedae, Carex macloviana, and Baccharis magellanica explained less than 30% in the same axis (Appendix 5). Cross-validation indicated that the best statistics were obtained for Blechnum penna-marina, Festuca gracillima, and Gaultheria mucronata (B > 0.90, P(B = 0) < 0.10, Bcont > 0.64, AVI > 0.49, CVI > 0.48). These outputs indicated that these species were mainly specialists. Nevertheless, the lower performances of cross-validation were obtained for Hordeum comosum and Juncus balticus (B < 0.13, P(B = 0) > 0.44, Bcont < − 0.04, AVI > 0.51, CVI < 0.39), indicating that these other species were more generalists than specialists (Appendix 6).
PHS maps presented remarkable differences in the spatial distribution (Appendix 7) and the habitat requirements (e.g. marginality and specialization) for each species (Fig. 3). Some species presented higher values of PHS in the steppes of the eastern areas of the province, showing the lowest specialization (1.60 to 7.54) and marginality (0.52 to 0.97) values. Among these species, nine (ADVO, CHAV, COSU, EPCH, FEAR, LYCH, MIRG, POLA, POLI) were related to a single ecological area, while four species (CLDA, PACH, CHAU, HOCO) were associated to two ecological areas, and ten species (ACPO, CAAR, MUTR, NABR, NAGL, NAUL, PACHR, PAIB, PASO, POSP) were associated to more ecological areas. Moreover, another species presented the highest PHS values in the western steppes near the ecotone, close to the mountain forests, showing low specialization values (2.06 to 6.76) and middle marginality values (1.35 to 2.16). Among these species, seven (AGPE, ARMA, BAMA, CAMA CAUN, HOPU, JUBA, PERE) were related to only one ecological area, while three species (AZPR, FEMA, RYVI) were associated to two ecological areas and six species (BEMI, BRSE, CAAN, FEGR, FEPA, SEFI) to more ecological areas. Finally, thirteen species showed the highest PHS values in a narrow area close to Los Andes Mountains, presenting the highest specialization (5.54 to 14.75) and marginality (1.85 to 2.89) values. Among these species, six (AGCA, ANMU, BEEM, BLPE, ESRU, VIMA) were related to only one ecological area, while five species (ACMA, CHDI, GAAP, GAMU, OSCH) were associated to two ecological areas and two species (AVFL, EMRU) to more ecological areas.
Potential biodiversity map of vascular plant species
The fitted PHS maps were combined into a single map, integrating all the selected vascular plant species (Fig. 4). The PBM presented the lowest values (1–51%) near the mountain forests and ice fields in the west, and medium values (52–62%) in the dry steppes in the east. The highest PBM values (63–100%) occurred in three different steppe areas: (i) one important area of sixteen hexagons in the south (4.00 million ha), (ii) eleven hexagons in the north area of the province (2.75 million ha), and (iii) the smaller area with five hexagons located in the central-east (1.25 million ha).
The analyses of the modelled environmental variables allowed us to understand the occurrence of different PB levels in the landscape (Fig. 5). Temperature variables greatly influenced PB (AMT: F = 14.25, p < 0.001; MAXWM: F = 14.58, p < 0.001; MINCM: F = 8.69, p < 0.001), e.g. medium and high PB qualities occurred in areas where the mean annual temperature was higher (8.0 °C) than the mean value of the whole province. Annual precipitation negatively influenced PB (F = 14.24, p < 0.001), e.g. low PB quality occurred in areas where rainfall was above the mean value of the province (246 mm year−1). The higher rainfall was related to the upper mountains above the tree-line and closeness to ice fields. Elevation (F = 21.64, p < 0.001) followed the same pattern, while other landscape variables (distance to lakes and rivers) did not significantly influence PB qualities. Finally, PB qualities increased with the global potential evapotranspiration (F = 13.20, p < 0.001), while extreme values (low and high qualities) were presented in areas with higher NDVI values (F = 4.57, p = 0.012).
PB greatly changed through the main ecological areas (F = 19.93, p < 0.001), where shrublands (SL) presented the highest values followed by humid (HS) and dry steppes (DS). The lowest PB values were found in the sub-Andean grasslands (SAG) and in the mountain forests and alpine vegetation (FAV) (Fig. 6). Considering the supporting and regulating ES proxies, soil organic carbon stock (F = 2.73, p = 0.069), soil total nitrogen stock (F = 3.16, p = 0.046), annual net primary productivity (F = 4.00, p = 0.021), and desertification index (F = 9.61, p < 0.001) greatly varied according to PB qualities. The highest ES values were related to soil nutrient stock and carbon sequestration, which were mainly associated with low and high PB qualities. The desertification index (reverse proxy of soil control erosion) increased with PB qualities. The provisioning ES proxy, sheep presence probability, significantly changed across PB qualities (F = 18.97, p < 0.001), increasing with PB quality. Finally, cultural ES proxies presented different connections with PB qualities: aesthetic (F = 6.84, p = 0.002), existence (F = 0.71, p = 0.492), and local identity (F = 3.14, p = 0.047) values decreased with PB qualities, and higher recreational values (F = 3.47; p = 0.035) were associated with higher PB qualities.
Potential habitat suitability of vascular plant species
The interest to understand species distribution at different scales (e.g. regional level) had been increased during the last years (Chen et al. 2018; Peri et al. 2019a). Nevertheless, the need of big data is a challenge in remote areas as Southern Patagonia (Martínez Pastur et al. 2016a). In this context, PHS modelling based on ENFA is one feasible alternative (Hirzel et al. 2002) that links the presence data with environmental variables (Hirzel and Le Lay 2008), which was used for understory plant species in forests of Patagonia (Martínez Pastur et al. 2016a; Rosas et al. 2019a). In our study, data presence belonged from different database networks (e.g. local and national) covering all the landscape and the different ecological areas of the Santa Cruz Province and include the most relevant species of the local flora (e.g. 15 indicator plants for each ecological area).
The PHS maps support previous vegetation studies (e.g. Oliva et al. 2004; Oyarzabal et al. 2018), where different climate and environmental drivers strongly influenced plant species distribution (Fig. 1). Besides this, these studies also determine that some species are representative of multiple ecological areas (Table 1), e.g. Festuca pallescens is one of the most conspicuous and wide-dispersed species in Patagonia, whereas some auto-ecological studies (e.g. seed germination) associate this species with cold environments (López et al. 2019) and under 400 mm year−1 (Mancini et al. 2012). These findings support our results, where high PHS values were related to sub-Andean grasslands in the west. In addition, Mancini et al. (2012) indicated that shrub species (e.g. Empetrum rubrum and Gaultheria mucronata) grow close to Nothofagus forests in the west, while Gargaglione et al. (2014) showed that Avenella flexuosa were associated to N. antarctica forests in open environments (e.g. ecotone between grasslands and mountain forests). Despite the species associated to different ecological areas, our ENFA results showed that their high marginality and specialization values indicated that these species tend to live in a narrow range of environmental conditions and where their optimum habitat differed from the mean environmental values of the province (Fig. 3). Rainfall gradient, which decreases from west to east, also influences vegetation distribution, e.g. Bertiller et al. (1995) identified in the extra-Andean steppes of Northern Patagonia that Festuca pallescens decreases while shrubs increases (e.g. Senecio filaginoides and Nassauvia glomerulosa) their cover along the rainfall gradient (from 600 to 170 mm year−1). In humid Magellanic grass steppes in the south, F. pallescens is also associated with Poa spiciformis and Carex andina (Peri and Lasagno 2010). However, in dry Magellanic grass steppes, F. gracillima is the dominant species accompanied by Nardophyllum bryoides and Nassauvia ulicina (Mancini et al. 2012). These distinct plant communities of steppes were mainly due to long-term differences in water availability (Peri et al. 2013). These studies support our results, where most of the species presented similar ecological requirements (e.g. low specialization and middle marginality values); however, N. bryoides, Nassauvia glomerulosa, and N. ulicina presented lower marginality values indicating that their optimum habitat is near to the mean environmental conditions of the province.
Other species presented a narrow distribution (e.g. two ecological areas) (Table 1), e.g. Acaena magellanica, Chiliotrichum diffusum, Galium aparine, and Osmorhiza chilensis. These species were identified by Huertas Herrera et al. (2018) growing in deciduous forests at lower elevations in Tierra del Fuego, Argentina. This is coincident with our results, where similar ecological requirements (e.g. high specialization and marginality values) and high PHS values were shown in forested areas and near humid steppes in the west. Other species presented a more restricted habitat (e.g. Baccharis magellanica), showing a middle specialization and high marginality values. Gargaglione et al. (2014) associated this species to open environments, e.g. gap grasslands surrounding N. antarctica forests. Other species presented the highest marginality values (e.g. Blechnum penna-marina and Viola magellanica) and were related to evergreen forest in humid areas, close overstory canopies (Martínez Pastur et al. 2012), and other forested areas where some shrub species (e.g. Escallonia rubra) occurred (Mancini et al. 2012).
Some species with high specialization values (e.g. Berberis empetrifolia) were related to extreme xeric conditions near the Andean Mountains (Bottini et al. 2000), while others (e.g. Agrostis capillaris) were associated to ecotone areas between grasslands and N. antarctica forests (Alonso et al. 2019). López et al. (2019) found that Poa ligularis was associated to steppes in Northern Patagonia due to some of their ecological requirements (e.g. seed germination was related to a higher temperature than Festuca pallescens). In our study, this species was related to the steppes in the north-west of the province (mountains and plateaus), where high PHS values were related to the dry steppe ecological area. In addition, Chuquiraga avellanedae, Pappostipa chrysophylla, P. sorianoi, Nassauvia ulicina, Lycium chilense, and Festuca argentina have been also described in these extreme natural environments (Oliva et al. 2004; Peri et al. 2013; Oyarzabal et al. 2018), where ENFA analyses showed low specialization and marginality values, and PHS values associated to the dry steppes.
Potential biodiversity map of vascular plant species
Usually, PHS maps of plants species have been used to link species occurrence with environmental variables (Dubuis et al. 2013; Pottier et al. 2013). Recently, new studies combine multiple maps to synthetizes the information of multiple species (Martínez Pastur et al. 2016a; Rosas et al. 2018), and particularly, Rosas et al. (2019a) create one PBM of understory species of forests in Santa Cruz. However, those studies focalized the analyses in particular ecosystems (e.g. forests), and not allowed the comparisons among distinct ecological areas. For example, most of the conservation efforts were focused on forests (Rosas et al. 2019b), due to the lack of information about the importance of grasslands and shrublands for conservation in the Patagonia (Peri et al. 2021). This study considered the entire region and included the different ecosystem types across all the ecological areas (n = 8, from dry steppes to alpine vegetation) and a greater number of plant species (fifteen indicator species per ecological area). Different studies in Patagonia have focused on floristic heterogeneity description (e.g. physiognomy, dominant species, structural heterogeneity) (Paruelo et al. 2004), e.g. Oyarzabal et al. (2018) have re-described the main vegetation types of Patagonia, and Oliva et al. (2004) made an update for Santa Cruz Province. However, the available information is still scarce about plant biodiversity and their relationships with the regional environmental variables. One useful study characterized Patagonian ecosystem based on different approaches using climate as the main proxy, e.g. life zones or functional variables (e.g. NDVI) (Paruelo et al. 2001; Derguy et al. 2019). These approaches refer to vegetation physiognomy but not to the observed vegetation cover in the field, where more particular drivers (e.g. environmental heterogeneity) can influenced local biodiversity (Li et al. 2020). Our PHS maps were coincident with different vegetation cover studies (Oliva et al. 2004; Oyarzabal et al. 2018), where our PBM allowed to improve ecosystem characterization by capturing potential biodiversity changes according to the different indicator species. In a general trend, PBM values increased with temperature (south to north) and evapotranspiration values, where shrublands and steppes were predominant, while decreased with precipitation and elevation (west to east), where forests and alpine vegetation prevail (Fig. 1). At the global scale, rainfall is strongly correlated with species richness along latitudinal gradients (Kreft and Jetz 2007), e.g. more richness was observed in rainy areas at lower tropical latitudes. In our study, low PB values were associated with higher precipitation values, while medium and high values of PB were related to low precipitation values. In our study area, the lowest biodiversity was related to dry steppes with the lower rainfall values located in the inner land. PB values increased across the rainfall gradient and closeness to seashores. However, below the close canopy of the mountain forest, the richness decreased despite the rainfall amounts, and in the upper mountains, the temperature becomes the limiting factor, influencing the number of plant species that can survive. Cleland et al. (2013) found a positive relationship between species richness and mean annual precipitation in grasslands of the USA. However, in Patagonia (46° 00′–52° 30′ S), biodiversity is more controlled by the availability of environmental temperature, where Kreft and Jetz (2007) found a significant positive effect for vascular plant species richness, supporting the described results.
Another challenge of this study was to link PB values with ES supply (e.g. Martínez Pastur et al. 2017) that can help to understand the role that plant biodiversity plays in the delivery of these services (MAES 2013) at the regional scale. Biodiversity is assumed to be critical for ES supply (MEA 2005), where services can be obtained only if ecosystems include the species richness that guarantees the functional processes (Cardinale et al. 2011; Thompson et al. 2011; Mori et al. 2017). In fact, some authors indicated that biodiversity is itself an ES, because it is the basis for nature-based tourism or regulation of diseases (Mace et al. 2012). Supporting ES also had been demonstrated to present a strong relationship with plant biodiversity (Cardinale et al. 2011; Chen et al. 2018; Peri et al. 2019a). In this study, the proxies used for each ES type were soil organic carbon stock (Peri et al. 2018), soil total nitrogen stock (Peri et al. 2019b), annual net primary productivity (Zhao and Running 2010), and desertification index (Del Valle et al. 1998). These proxies were previously proposed by several authors for similar studies (e.g. Stephens et al. 2015; Martínez Pastur et al. 2017; Chen et al. 2018; Wen et al. 2020) and were related with ecosystem functions and plant biodiversity considering different management scenarios (Wang et al. 2017), e.g. Peri et al. (2019a) found that soil carbon was a powerful predictor for threatened vascular plant biodiversity in Southern Patagonia. In our study, the higher values of ES proxies occurred at both extremes of PB qualities (low and high), e.g. low qualities were related to Nothofagus forests and high qualities to humid steppes and shrublands. Experimental studies showed that plant diversity increased their ES by improving soil microbial diversity and activity of grasslands (Fornara and Tilman 2008). Native Patagonian forests presented lower PB values, where high ES values were mainly related to the environmental conditions that improve organic residues and soil microbial biomass (Peri et al. 2016c, 2018, 2019b). In this context, Peri et al. (2017) found that N. antarctica forests presented more soil organic carbon stock than other temperate forests. Provisioning ES were mainly related to regional economic activities (MEA 2005) and were represented here by sheep presence probability (Pedrana et al. 2010). This proxy increased with PB values, where humid steppes and shrublands prevail. Both areas support sheep and cattle livestock grazing (Peri et al. 2016a), where some plant species (e.g. Festuca gracillima) constitutes about one-third of forage intake during winter (Oliva et al. 2005). Livestock grazing reduces plant species diversity, productivity, and vegetation cover and induces changes in soil structure and nutrient contents (Jiang et al. 2011; Dlamini et al. 2016). Peri et al. (2016b) indicate a negative effect on plant biodiversity due to continuous overgrazing in heterogeneous large paddocks in Patagonia. The steppe vulnerability is widely recognized (Gaitán et al. 2019), where intensive grazing decreases carbon and nitrogen stocks and increases desertification, generating losses in the ES supply (Del Valle et al. 1998; Peri et al. 2016b). The supply of cultural ES presented complex relationships with biodiversity, where particular vegetation types (e.g. forests) are closely related with high provision levels (Martínez Pastur et al. 2016a) contributing to different dimensions of human well-being (Vilardy et al. 2011; Russell et al. 2013). In our study, aesthetic, existence and local identity were lower than recreational values at high PB qualities. Martínez Pastur et al. (2016b) identified that most of the cultural ES in Santa Cruz were influenced by the closeness to water bodies and mountains (low PB values), while recreational values were influenced by the accessibility to cities and main routes in the steppes (low PB values) (Rosas et al. 2019b). According to these results, provisioning ES can generate trade-offs with the biodiversity conservation at the regional scale, while cultural ES can produce synergies with the biodiversity, allowing the creation of natural reserves (Rosas et al. 2019a).
Several human-related activities in Southern Patagonia (e.g. livestock) negatively influenced the original ecosystems by modifying the plant biodiversity, soil properties, and structure (Peri et al. 2013, 2016b, 2016c). At the regional level, most of the natural reserves are located close to the Andes Mountains, protecting mainly native forests (N. pumilio and N. betuloides) and specific ES related to tourism (e.g. aesthetic ES) (Martínez Pastur et al. 2016b). However, N. antarctica forests presented the highest PB values (Rosas et al. 2019a), and less than 20% of these forests are under formal protection (e.g. National Parks or Provincial Reserves). This highlights the importance of conservation strategies on private lands (e.g. land-sharing strategy), where most of the economic activities influence plant biodiversity (Peri et al. 2016b). There is an increasing interest to integrate ES arguments within management plans, where new strategies (e.g. silvopastoral systems) have been developed to reconciles the productive needs and requirements of local people with biodiversity conservation (Peri et al. 2016c). In the other extreme, Patagonian steppes presented lower natural reserves than any other ecological region (e.g. Bosques Petrificados Natural Monument and Monte León National Park), and where most of them are located near the sea coast. Steppe areas presented more complex interactions with the environment and ES; however, a general trend showed that high PB values are coincident with high values of different ES supplies (provisioning, regulating, and supporting). For more than 100 years, livestock grazing influenced and modelled the region (Peri 2011) in large paddocks that varied from 1000 to 20,000 ha (Ormaechea and Peri 2015), increasing the desertification processes (Del Valle et al. 1998). Bjerring et al. (2020) experimentally demonstrated that the adjustment of the stocking rate or rotational grazing had a more positive effect on plant biodiversity and biomass growth than continuous grazing in the steppes. Some grazing managements, as warm-season grazing, improve ES delivery and biodiversity conservation in temperate steppes of northern China (Wang et al. 2017). This sustainable management reduces grazing intensity using specific areas during summer and autumn, and it is considered as an appropriate management strategy for maintaining plant species diversity and soil texture (Cingolani et al. 2005; Bjerring et al. 2020). In addition, this type of management is more efficient when some paddocks were excluded (throughout the year by fencing) due to degradation of ES delivery and biodiversity in the temperate steppes (Wang et al. 2016). To date, there are no management strategies that protect the biodiversity (e.g. land sharing) (Fischer et al. 2014), where shrublands are identified as an obstacle for livestock, e.g. some management proposals promote the removal of the shrubs to increase grass cover (Sola et al. 2016). It is necessary to reconcile these management proposals and the maintenance of the biodiversity in the hotspot areas identified in this work. The regional approach of PBM of the most relevant plants for each regional vegetation type allows us to improve the knowledge about plant potential habitat suitability and supports other studies about vegetation description at the regional level. Moreover, PBM allowed us to relate plant biodiversity and ES supply and help us to understand their relationships to identify potential negative impacts and trade-offs with economic activities.
Potential habitat suitability models using the Biomapper software allowed us to develop maps of relevant indicator vascular plant species at the landscape level using the presence data only and environmental variables (e.g. climate, topography) free availability on the public internet. ENFA indexes (marginality and specialization) allowed us to characterize plant habitat requirements and link them to environmental gradients of the landscape, helping in categorizing the plants according to its distribution in the landscape. The final map of potential biodiversity synthetized the information of the different plant species and assisted to identify hotspot areas across the province (e.g. mainly in humid steppes and shrublands). These areas were outside of the formal reserve network, and they are not included in the conservation strategies implemented in the region. In addition, the link between potential biodiversity and ES allowed us to understand potential trade-offs and synergies across the landscape and for the different ecological areas (e.g. from dry steppes to alpine vegetation). Areas with the greatest biodiversity values also showed high provisioning ES, and this spatial congruence determinates potential trade-off with conservation and other ES supply. The proposals explored in this paper is an effective tool for areas with low availability of databases to detect biodiversity hotspots and potential trade-offs that can be rapidly incorporated into decision-making to raise better spatial planning for plant biodiversity conservation.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Annual mean temperature
Analysis of variance
Annual net primary productivity
Absolute validation index
Continuous Boyce index
Central plateau steppes
Contrast validation index
Distance to lakes
Dry Magellanic grass steppes
Distance to rivers
Environmental niche factor analysis
Global potential evapotranspiration
Forestal, Agrícola y Manejo del Agua of INTA EEA-Santa Cruz
Forests and alpine vegetation
Humid Magellanic grass steppes
Local identity values
Max temperature of the warmest month
Min temperature of the coldest month
Mountains and plateaus
- N :
Normalized difference vegetation index
- P :
Proportion of validation points
Potential biodiversity map
Parcelas de Ecología y Biodiversidad de Ambientes Naturales en Patagonia Austral
Potential habitability suitability
Soil organic carbon
Sheep presence probability
Shrub-steppe San Jorge Gulf
Soil total nitrogen
Abdelaal M, Fois M, Dakhil MA, Bacchetta G, El-Sherbeny GA (2020) Predicting the potential current and future distribution of the endangered endemic vascular plant Primula boveana Decne. ex Duby in Egypt. Plants 9(8):957
Alonso MF, Wentzel H, Schmidt A, Balocchi O (2019) Plant community shifts along tree canopy cover gradients in grazed Patagonian Nothofagus antarctica forests and grasslands. Agrofor Syst 94:651–661
Barbier S, Gosselin F, Balandier P (2008) Influence of tree species on understory vegetation diversity and mechanisms involved a critical review for temperate and boreal forests. For Ecol Manag 254(1):1–15. https://doi.org/10.1016/j.foreco.2007.09.038
Bertiller MB, Elissalde NO, Rostagno CM, Defossé GE (1995) Environmental patterns and plant distribution along a precipitation gradient in western Patagonia. J Arid Environ 29(1):85–97. https://doi.org/10.1016/S0140-1963(95)80066-2
Bjerring AT, Peri PL, Christiansen R, Vargas-Bello-Pérez E, Hansen HH (2020) Rangeland grazing management in Argentine Patagonia. Int J Agric Biol 24:1041–1052
Bottini MCJ, Greizerstein EJ, Aulicino MB, Poggio L (2000) Relationships among genome size, environmental conditions and geographical distribution in natural populations of NW Patagonian species of Berberis L. (Berberidaceae). Ann Bot 86(3):565–573. https://doi.org/10.1006/anbo.2000.1218
Boyce MS, Vernier PR, Nielsen SE, Schmiegelow F (2002) Evaluating resource selection functions. Ecol Model 157(2-3):281–300. https://doi.org/10.1016/S0304-3800(02)00200-4
Bradley BA, Olsson AD, Wang O, Dickson BG, Pelech L, Sesnie SE, Zachmann LJ (2012) Species detection vs. habitat suitability: are we biasing habitat suitability models with remotely sensed data? Ecol Model 244:57–64. https://doi.org/10.1016/j.ecolmodel.2012.06.019
Cardinale BJ (2012) Biodiversity loss and its impact on humanity. Nature 486(7401):59–67. https://doi.org/10.1038/nature11148
Cardinale BJ, Matulich KL, Hooper DU, Byrnes JE, Duffy E, Gamfeldt L, Balvanera P, O’Connor ML, Gonzalez A (2011) The functional role of producer diversity in ecosystems. Am J Bot 98(3):572–592. https://doi.org/10.3732/ajb.1000364
Chai SL, Zhang J, Nixon A, Nielsen S (2016) Using risk assessment and habitat suitability models to prioritise invasive species for management in a changing climate. PLoS One 11(10):e0165292. https://doi.org/10.1371/journal.pone.0165292
Chen S, Wang W, Xu W, Wang Y, Wan H, Chen D, Tang Z, Tang X, Zhou G, Xie Z, Zhou D, Shamgguan Z, Huang J, He JS, Wang Y, Sheng J, Tang L, Li X, Dong M, Wu Y, Wang Q, Wang Z, Wu J, Chaplin FS, Bai Y (2018) Plant diversity enhances productivity and soil carbon storage. PNAS 115(16):4027–4403. https://doi.org/10.1073/pnas.1700298114
Cingolani AM, Posse G, Collantes MB (2005) Plant functional traits, herbivore selectivity and response to sheep grazing in Patagonian steppe grasslands. J Appl Ecol 42(1):50–59. https://doi.org/10.1111/j.1365-2664.2004.00978.x
Cleland EE, Collins SL, Dickson TL, Farrer EC, Gross KL, Gherardi LA, Hallett LM, Hodds RJ, Hsu JS, Turnbull L, Suding KN (2013) Sensitivity of grassland plant community composition to spatial vs. temporal variation in precipitation. Ecology 94(8):1687–1696. https://doi.org/10.1890/12-1006.1
Del Valle HF, Elissalde NO, Gagliardini DA, Milovich J (1998) Status of desertification in the Patagonian region: assessment and mapping from satellite imagery. Arid Land Res Manag 12(2):95–121. https://doi.org/10.1080/15324989809381502
Derguy MR, Frangi JL, Drozd AA, Arturi MF, Martinuzzi S (2019) Holdridge life zone map: Republic of Argentina. Gen Tech Rep IITF-GTR-51
Dlamini P, Chivenge P, Chaplot V (2016) Overgrazing decreases soil organic carbon stocks the most under dry climates and low soil pH: a meta-analysis shows. Agric Ecosyst Environ 221:258–269. https://doi.org/10.1016/j.agee.2016.01.026
Dubuis A, Giovanettina S, Pellissier L, Pottier J, Vittoz P, Guisan A (2013) Improving the prediction of plant species distribution and community composition by adding edaphic to topo-climatic variables. J Veg Sci 24(4):593–606. https://doi.org/10.1111/jvs.12002
ESRI (2011) ArcGIS Desktop: Release 10 Environmental Systems Research Institute. Inc, Redlands, USA.
Farr TG, Rosen PA, Caro E, Crippen R, Duren R, Hensley S, Kobrick M, Paller M, Rodriguez E, Roth L, Seal D, Shaffer S, Shimada J, Umland J, Werner M, Oskin M, Burbank D, Alsdorf D (2007) The shuttle radar topography mission. Rev Geophys 45:RG2004
Fischer J, Abson DJ, Butsic V, Chappell MJ, Ekroos J, Hanspach J, Wehrden H (2014) Land sparing versus land sharing: moving forward. Conserv Lett 7(3):149–157. https://doi.org/10.1111/conl.12084
Fornara DA, Tilman D (2008) Plant functional composition influences rates of soil carbon and nitrogen accumulation. J Ecol 96(2):314–322. https://doi.org/10.1111/j.1365-2745.2007.01345.x
Gaitán JJ, Bran DE, Oliva GE, Stressors PA (2019) Patagonian Desert. In: Patagonian desert. Encyclopaedia of the World’s Biomes, Elsevier, Amsterdam, Netherlands
Gargaglione V, Peri PL, Rubio G (2014) Tree–grass interactions for N in Nothofagus antarctica silvopastoral systems: evidence of facilitation from trees to underneath grasses. Agrofor Syst 88(5):779–790. https://doi.org/10.1007/s10457-014-9724-3
Guisan A, Zimmermann NE (2000) Predictive habitat distribution models in ecology. Ecol Model 135(2-3):147–186. https://doi.org/10.1016/S0304-3800(00)00354-9
Haines-Young R, Potschin MB (2018) Common international classification of ecosystem services (CICES) V5.1 and guidance on the application of the revised structure. CICES, London, UK
Hijmans RJ, Cameron SE, Parra JL, Jones PG, Jarvis A (2005) Very high-resolution interpolated climate surfaces for global land areas. Int J Climatol 25(15):1965–1978. https://doi.org/10.1002/joc.1276
Hirzel AH, Arlettaz R (2003) Modelling habitat suitability for complex species distributions by the environmental-distance geometric mean. Environ Manag 32(5):614–623. https://doi.org/10.1007/s00267-003-0040-3
Hirzel AH, Hausser J, Chessel D, Perrin N (2002) Ecological-niche factor analysis: how to compute habitat-suitability maps without absence data? Ecology 83:2027–2036
Hirzel AH, Hausser J, Perrin N (2004) Biomapper 3.1. Division of conservation biology, Bern, Switzerland
Hirzel AH, Helfer V, Metral F (2001) Assessing habitat-suitability models with a virtual species. Ecol Model 145(2-3):111–121. https://doi.org/10.1016/S0304-3800(01)00396-9
Hirzel AH, Le Lay G (2008) Habitat suitability modelling and niche theory. J Appl Ecol 45(5):1372–1381. https://doi.org/10.1111/j.1365-2664.2008.01524.x
Hirzel AH, Le Lay G, Helfer V, Randin C, Guisan A (2006) Evaluating habitat suitability models with presence-only data. Ecol Model 199(2):142–152. https://doi.org/10.1016/j.ecolmodel.2006.05.017
Huertas Herrera A, Cellini JM, Barrera M, Lencinas MV, Martínez Pastur G (2018) Environment and anthropogenic impacts as main drivers of plant assemblages in forest mountain landscapes of Southern Patagonia. For Ecol Manag 430:380–393. https://doi.org/10.1016/j.foreco.2018.08.033
Hutchinson GE (1957) Concluding remarks. Cold Spring Harb Symp Quant Biol 22:145–159. https://doi.org/10.1101/SQB.1957.022.01.039
Jiang LL, Han XG, Dong N, Wang YF, Kardol P (2011) Plant species effects on soil carbon and nitrogen dynamics in a temperate steppe of northern China. Plant Soil 346(1-2):331–347. https://doi.org/10.1007/s11104-011-0822-y
Jordan SE, Palmquist KA, Bradford JB, Lauenroth WK (2020) Soil water availability shapes species richness in mid-latitude shrub steppe plant communities. J Veg Sci 31(4):646–657. https://doi.org/10.1111/jvs.12874
Kohler M, Devaux C, Grigulis K, Leitinger G, Lavorel S, Tappeiner U (2017) Plant functional assemblages as indicators of the resilience of grassland ecosystem service provision. Ecol Indic 73:118–127. https://doi.org/10.1016/j.ecolind.2016.09.024
Kreft H, Jetz W (2007) Global patterns and determinants of vascular plant diversity. PNAS 104(14):5925–5930. https://doi.org/10.1073/pnas.0608361104
Lencinas MV, Martínez Pastur G, Rivero P, Busso C (2008) Conservation value of timber quality vs associated non-timber quality stands for understory diversity in Nothofagus forests. Biodivers Conserv 17(11):2579–2597. https://doi.org/10.1007/s10531-008-9323-6
Li M, Zhang X, Niu B, He Y, Wang X, Wu J (2020) Changes in plant species richness distribution in Tibetan alpine grasslands under different precipitation scenarios. Glob Ecol Conserv 21:e00848. https://doi.org/10.1016/j.gecco.2019.e00848
Lillesand TM, Kiefer RW (2000) Remote sensing and image interpretation. John Wiley & Sons, New York, USA
López AS, Marchelli P, Batlla D, López DR, Arana MV (2019) Seed responses to temperature indicate different germination strategies among Festuca pallescens populations from semi-arid environments in North Patagonia. Agric For Meteorol 272:81–90
Ma T, Deng X, Chen L, Xiang W (2020) The soil properties and their effects on plant diversity in different degrees of rocky desertification. Sci Total Environ 736:e139667
Mace G, Norris K, Fitter A (2012) Biodiversity and ecosystem services: a multi-layered relationship. Trends Ecol Evol 27(1):19–26. https://doi.org/10.1016/j.tree.2011.08.006
MAES (2013) An analytical framework for ecosystem assessments under Action 5 of the EU Biodiversity Strategy to 2020 Discussion Paper. Publications Office of the European Union. Amsterdam, Netherlands, Luxembourg
Mancini MV, de Porras ME, Bamonte FP (2012) Southernmost South America steppes: vegetation and its modern pollen-assemblages representation. In: Germanno DM (ed) Steppe ecosystems: Dynamics, land use and conservation. Nova Science Publishers, Nueva York, USA.
Martínez Pastur G, Jordan C, Soler Esteban R, Lencinas MV, Ivancich H, Kreps G (2012) Landscape and microenvironmental conditions influence over regeneration dynamics in old-growth Nothofagus betuloides Southern Patagonian forests. Plant Biosyst 146(1):201–213. https://doi.org/10.1080/11263504.2011.650725
Martínez Pastur G, Peri PL, Huertas Herrera A, Schindler S, Díaz-Delgado R, Lencinas MV, Soler R (2017) Linking potential biodiversity and three ecosystem services in silvopastoral managed forest landscapes of Tierra del Fuego, Argentina. Int J Biodiv Soc Ecosyst Serv Manage 13:1–11
Martínez Pastur G, Peri PL, Lencinas MV, García Llorente M, Martín López B (2016b) Spatial patterns of cultural ecosystem services provision in Southern Patagonia. Landsc Ecol 31(2):383–399. https://doi.org/10.1007/s10980-015-0254-9
Martínez Pastur G, Peri PL, Soler Esteban R, Schindler S, Lencinas MV (2016a) Biodiversity potential of Nothofagus forests in Tierra del Fuego (Argentina): tools for regional conservation planning. Biodivers Conserv 25(10):1843–1862. https://doi.org/10.1007/s10531-016-1162-2
MEA (2005) Ecosystems and human wellbeing: current state and trends. Millennium Ecosystem Assessment, Washington, USA
Mori AS, Lertzman KP, Gustafsson L (2017) Biodiversity and ecosystem services in forest ecosystems: a research agenda for applied forest ecology. J Appl Ecol 54(1):12–27. https://doi.org/10.1111/1365-2664.12669
Oliva G, Collantes M, Humano G (2005) Demography of grazed tussock grass populations in Patagonia. Range Ecol Manage 58(5):466–473. https://doi.org/10.2111/1551-5028(2005)58[466:DOGTGP]2.0.CO;2
Oliva G, Gonzalez L, Ruial P (2004) Áreas Ecológicas. In: Gonzalez L, Rial P (eds) Guía Geográfica Interactiva de Santa Cruz. INTA, Rio Gallegos, Santa Cruz
Ormaechea S, Peri PL (2015) Landscape heterogeneity influences on sheep habits under extensive grazing management in Southern Patagonia. Livest Res Rural Dev 27:1–11
ORNL DAAC (2008) MODIS Collection 5 Land Products Global Sub-setting and Visualization Tool. ORNL DAAC, Oak Ridge, Tennessee, USA
Oyarzabal M, Clavijo J, Oakley L, Biganzoli F, Tognetti P, Barberis I, Maturo HM, Aragon R, Campanello P, Prado D, Oesterheld M, León JC (2018) Unidades de vegetación de la Argentina. Ecol Austral 28(1):40–63. https://doi.org/10.25260/EA.126.96.36.199.399
Paruelo JM, Golluscio RA, Guerschman JP, Cesa A, Jouve VV, Garbulsky MF (2004) Regional scale relationships between ecosystem structure and functioning: the case of the Patagonian steppes. Glob Ecol Biogeogr 13(5):385–395. https://doi.org/10.1111/j.1466-822X.2004.00118.x
Paruelo JM, Jobbágy EG, Sala OE (2001) Current distribution of ecosystem functional types in temperate South America. Ecosystems 4(7):683–698. https://doi.org/10.1007/s10021-001-0037-9
Pedrana J, Bustamante J, Travaini A, Rodríguez A (2010) Factors influencing guanaco distribution in southern Argentine Patagonia and implications for its sustainable use. Biodivers Conserv 19(12):3499–3512. https://doi.org/10.1007/s10531-010-9910-1
Peri PL (2011) Carbon storage in cold temperate ecosystems in Southern Patagonia, Argentina. In: Atazadeh I (ed) Biomass and remote sensing of biomass. InTech Publisher, Zagreb, Croatia
Peri PL, Banegas N, Gasparri I, Carranza C, Rossner B, Martínez Pastur G, Caballero L, López D, Loto D, Fernández P, Powel P, Ledesma M, Pedraza R, Albanesi A, Bahamonde HA, Eclesia R, Piñeiro G (2017) Carbon sequestration in temperate silvopastoral systems, Argentina. In: Montagnini F (ed) Integrating landscapes: agroforestry for biodiversity conservation and food sovereignty. Springer Series: Advances in Agroforestry, Charm, Switzerland
Peri PL, Hansen NE, Bahamonde HA, Lencinas MV, Von Müller AR, Ormaechea S, Gargaglione V, Soler Esteban R, Tejera L, Lloyd CE, Martínez Pastur G (2016c) Silvopastoral systems under native forest in Patagonia, Argentina. In: Peri PL, Dube F, Varella A (eds) Silvopastoral systems in southern South America. Springer, Series: Advances in Agroforestry, Cham, Switzerland
Peri PL, Ladd B, Lasagno RG, Martínez Pastur G (2016b) The effects of land management (grazing intensity) vs the effects of topography, soil properties, vegetation type, and climate on soil carbon concentration in Southern Patagonia. J Arid Environ 134:73–78. https://doi.org/10.1016/j.jaridenv.2016.06.017
Peri PL, Lasagno RG (2010) Biomass, carbon and nutrient storage for dominant grasses of cold temperate steppe grasslands in southern Patagonia, Argentina. J Arid Environ 74(1):23–34. https://doi.org/10.1016/j.jaridenv.2009.06.015
Peri PL, Lasagno RG, Martínez Pastur G, Atkinson R, Thomas E, Ladd B (2019a) Soil carbon is a useful surrogate for conservation planning in developing nations. Sci Rep 9:e3905
Peri PL, Lencinas MV, Bousson J, Lasagno R, Soler R, Bahamonde H, Pastur GM (2016a) Biodiversity and ecological long-term plots in Southern Patagonia to support sustainable land management: the case of PEBANPA network. J Nat Conserv 34:51–64. https://doi.org/10.1016/j.jnc.2016.09.003
Peri PL, Lencinas MV, Martínez Pastur G, Wardell-Johnson GW, Lasagno R (2013) Diversity patterns in the steppe of Argentinean southern Patagonia: environmental drivers and impact of grazing. In: Morales MB, Traba Diaz J (eds) Steppe ecosystems: biological diversity, management and restoration. Nova Science Publishers, New York, USA
Peri PL, Monelos LH, Diaz BG, Mattenet FJ, Huertas LM, Bahamonde HA, Rosas YM, Lencinas MV, Cellini JM, Martínez Pastur G (2019c) Estado y uso de los bosques nativos de lenga, siempreverdes y mixtos de Santa Cruz: base para su conservación y manejo. INTA, Santa Cruz, Río Gallegos, Argentina
Peri PL, Nahuelhual L, Martínez Pastur G (2021) In: Springer Nature: Natural and Social Sciences of Patagonia (ed) Ecosystem services in Patagonia: a multi-criteria approach for an integrated assessment. Springer, Cham, Switzerland. https://doi.org/10.1007/978-3-030-69166-0
Peri PL, Rosas YM, Ladd B, Toledo S, Lasagno RG, Martínez Pastur G (2018) Modelling soil carbon content in South Patagonia and evaluating changes according to climate, vegetation, desertification and grazing. Sustainability 10:e438
Peri PL, Rosas YM, Ladd B, Toledo S, Lasagno RG, Martínez Pastur G (2019b) Modelling soil nitrogen content in South Patagonia across a climate gradient, vegetation type, and grazing. Sustainability 11:e2707
Pires AP, Srivastava DS, Marino NA, MacDonald AAM, Figueiredo-Barros MP, Farjalla VF (2018) Interactive effects of climate change and biodiversity loss on ecosystem functioning. Ecology 99(5):1203–1213. https://doi.org/10.1002/ecy.2202
Pottier J, Dubuis A, Pellissier L, Maiorano L, Rossier L, Randin CF, Vittoz P, Guisan A (2013) The accuracy of plant assemblage prediction from species distribution models varies along environmental gradients. Glob Ecol Biogeogr 22(1):52–63. https://doi.org/10.1111/j.1466-8238.2012.00790.x
Riesch R, Plath M, Bierbach D (2018) Ecology and evolution along environmental gradients. Curr Zool 64(2):193–196. https://doi.org/10.1093/cz/zoy015
Rosas YM, Peri PL, Bahamonde HA, Cellini JM, Barrera MD, Huertas Herrera A, Lencinas MV, Martínez Pastur G (2019b) Trade-offs between management and conservation for the provision of ecosystem services in the southern Patagonian forests. In: Stanturf J (ed) Achieving sustainable management of boreal and temperate forests. Burleigh Dodds Science Publishing, Cambridge, UK. https://doi.org/10.19103/AS.2019.0057.07
Rosas YM, Peri PL, Carrara R, Flores GE, Pedrana J, Martínez Pastur G (2019c) Potential biodiversity map of darkling beetles (Tenebrionidae): environmental characterization, land-uses and analyses of protection areas in Southern Patagonia. J In Conserv 23:885–897
Rosas YM, Peri PL, Huertas Herrera A, Pastore H, Martínez Pastur G (2017) Modelling of potential habitat suitability of Hippocamelus bisulcus: effectiveness of a protected areas network in Southern Patagonia. Ecol Process 6:28
Rosas YM, Peri PL, Lencinas MV, Martínez Pastur G (2019a) Potential biodiversity map of understory plants for Nothofagus forests in Southern Patagonia: analyses of landscape, ecological niche and conservation values. Sci Total Environ 682:301–309. https://doi.org/10.1016/j.scitotenv.2019.05.179
Rosas YM, Peri PL, Martínez Pastur G (2018) Potential biodiversity map of lizard species in Southern Patagonia: environmental characterization, desertification influence and analyses of protection areas. Amphib-Reptil 3:289–301
Russell R, Guerry AD, Balvanera P, Gould RK, Basurto X, Chan KMA, Klain S, Levine J, Tam J (2013) Humans and nature: how knowing and experiencing nature affect well-being. Annu Rev Environ Resour 38(1):473–502. https://doi.org/10.1146/annurev-environ-012312-110838
Schneiders A, Van Daele T, Van Landuyt W, Van Reeth W (2012) Biodiversity and ecosystem services: complementary approaches for ecosystem management? Ecol Indic 21:123–133. https://doi.org/10.1016/j.ecolind.2011.06.021
Shih SS (2020) Spatial habitat suitability models of mangroves with Kandelia obovate. Forests 11(4):477–496. https://doi.org/10.3390/f11040477
Silva LD, Costa H, De Azevedo EB, Medeiros V, Alves M, Elias RB, Silva L (2017) Modelling native and invasive woody species: a comparison of ENFA and MaxEnt applied to the Azorean forest. In: Pinto A, Zilberman D (eds) Modelling, dynamics, optimization and bioeconomics. Springer, Cham, Switzerland. https://doi.org/10.1007/978-3-319-55236-1_20
Sola FJ, Peri PL, Huertas L, Pastur GM, Lencinas MV (2016) Above-ground arthropod community structure and influence of structural-retention management in southern Patagonian scrublands, Argentina. J Insect Conserv 20(6):929–944. https://doi.org/10.1007/s10841-016-9918-2
Stein A, Gerstner K, Kreft H (2014) Environmental heterogeneity as a universal driver of species richness across taxa, biomes and spatial scales. Ecol Lett 17(7):866–880. https://doi.org/10.1111/ele.12277
Stephens PA, Pettorelli N, Barlow J, Whittingham MJ, Cadotte MW (2015) Management by proxy? The use of indices in applied ecology. J Appl Ecol 52(1):1–6. https://doi.org/10.1111/1365-2664.12383
Thompson ID, Okabe K, Tylianakis JM, Kumar P, Brockerhoff EG, Schellhorn NA, Parrotta JA, Nasi R (2011) Forest biodiversity and the delivery of ecosystem goods and services: translating science into policy. BioScience 61(12):972–981. https://doi.org/10.1525/bio.2011.61.12.7
Vilardy SP, González JA, Martín-López B, Montes C (2011) Relationships between hydrological regime and ecosystem services supply in a Caribbean coastal wetland: a social-ecological approach. Hydrol Sci J 56(8):1423–1435. https://doi.org/10.1080/02626667.2011.631497
Wan JZ, Wang CJ (2018) Expansion risk of invasive plants in regions of high plant diversity: a global assessment using 36 species. Ecol Inform 46:8–18. https://doi.org/10.1016/j.ecoinf.2018.04.004
Wang K, Deng L, Ren Z, Li J, Shangguan Z (2016) Grazing exclusion significantly improves grassland ecosystem C and N pools in a desert steppe of Northwest China. Catena 137:441–448. https://doi.org/10.1016/j.catena.2015.10.018
Wang T, Zhang Z, Li Z, Li P (2017) Grazing management affects plant diversity and soil properties in a temperate steppe in northern China. Catena 158:141–147. https://doi.org/10.1016/j.catena.2017.06.020
Wen Z, Zheng H, Zhao H, Xie S, Liu L, Ouyang Z (2020) Land-use intensity indirectly affects soil multifunctionality via a cascade effect of plant diversity on soil bacterial diversity. Glob Ecol Conserv 23:e01061. https://doi.org/10.1016/j.gecco.2020.e01061
Wiersma YF, Huettmann F, Drew CA (2011) Introduction landscape modelling of species and their habitats: history, uncertainty, and complexity. In: Drew CA, Wiersma YF, Huettmann F (eds) Predictive species and habitat modelling in landscape ecology. Springer, New York, USA. https://doi.org/10.1007/978-1-4419-7390-0_1
Wulff AS, Hollingsworth PM, Ahrends A, Jaffré T, Veillon JM, L’Huillier L, Fogliani B (2013) Conservation priorities in a biodiversity hotspot: analysis of narrow endemic plant species in New Caledonia. PLoS ONE 8(9):e73371. https://doi.org/10.1371/journal.pone.0073371
Xu H, Cao M, Wu Y, Cai L, Cao Y, Wu J, Lei J, Le Z, Ding H, Cui P (2016) Disentangling the determinants of species richness of vascular plants and mammals from national to regional scales. Sci Rep 6:21988
Zhao M, Running SW (2010) Drought-induced reduction in global terrestrial net primary production from 2000 through 2009. Science 329(5994):940–943. https://doi.org/10.1126/science.1192666
Zomer RJ, Trabucco A, Bossio DA, Van Straaten O, Verchot LV (2008) Climate change mitigation: a spatial analysis of global land suitability for clean development mechanism afforestation and reforestation. Agric Ecosyst Environ 126(1-2):67–80. https://doi.org/10.1016/j.agee.2008.01.014
This research is part of the doctoral thesis of YMR (Facultad de Ciencias Agrarias y Forestales, Universidad Nacional de la Plata).
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Rosas, Y.M., Peri, P.L., Lencinas, M.V. et al. Improving the knowledge of plant potential biodiversity-ecosystem services links using maps at the regional level in Southern Patagonia. Ecol Process 10, 53 (2021). https://doi.org/10.1186/s13717-021-00326-0
- Habitat suitability
- Environmental variables
- Ecosystem functions
- Conservation management
- Ecosystem services
- Landscape modelling