Abstract
Multiple-use management of spatially heterogeneous arid ecosystems faces many challenges. In this study, an approach is introduced for multiple-use management of arid ecosystems in Esfandaqeh rangelands, south east of Iran. The ecological, social, and economic values of plant species were, respectively, determined using field data, the number of people consumption, and the market price for a given species. Determined ecological, social, and economic values were then weighted based on experts' opinion, and the total sum of weighted values was considered as the total value of each species. The value of plant communities was estimated with respect to their plant composition. Changes in plant communities due to different uses were plotted based on state and transition model. According to the results, the grazing intensity was lower in plant communities with diverse uses compared to the less diverse ones. There were significant relationships between species diversity and plant communities’ values (P < 0.01), but some communities with low species diversity had high total value due to the presence of important species such as Pistacia atlantica. Total community value increased with raising the ecosystem potential for multiple use. The highest community value belonged to the upstream shrubland with no trade-off between plants collecting and grazing due to the presence of medicinal and edible plants. There were degraded states where spot management is needed to restore them to a balanced state. The developed approach for multiple-use management helps land managers for sustainable development and maximum use of arid ecosystems.
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Introduction
Arid lands constitute a significant portion of globe’ lands (about 41.3%) and are home to 2.1 billion people (Koohafkan and Stewart 2008). These lands have experienced numerous environmental and managerial disturbances altering their structure and function (Havstad et al. 2007; Quetier et al. 2007). Many arid ecosystems are threatened by unsustainable uses (Biggs et al. 2008), which lead to land degradation consequently. Degradation is a common concept that hinders land management from achieving multiple goals. Most arid ecosystems consist of a non-uniform species composition that requires heterogeneous management for their sustainable development (McGranahan and Kirkman 2013).
There are new paradigms on the basis that landscapes or ecosystems have multiple functions and the concept of single-purpose land use has recently changed (O'Farrell and Anderson 2010). Multifunctionality describes the capacity of an ecosystem to provide multiple socio-economic and ecological benefits to society (Hölting et al. 2019). Although this concept does not yet have specific implementation (Hölting et al. 2019), multiple-use management has been increasingly practiced in rangelands during the last two decades. Rangelands are multifunctional ecosystems providing multiple ecosystem services. Forage production is one of services that is very important in rangeland management. Traditional rangeland management focuses on forage production (Holechek et al. 2004), but in multiple-use management, the approaches focusing on forage production are not efficient and other uses are also considered. The management approaches designed based on multiple-use concept can increase plants vigor in rangelands and enhance locals’ incentives to protect natural plant communities (Havstad et al. 2007). Therefore, forage-based management should be replaced with holistic rangeland management, in which forage production is treated the same as other ecosystem functions and receives no more value. Multiple-use management increases stakeholder income while sustaining the exploitation of rangelands (Sabogal et al. 2013). Furthermore, there is more social support for conservation multifunctional ecosystems where higher numbers of services are provided (Garcìa-Llorente et al. 2012).
On the one hand, rangelands are cohesive units that are ecologically, economically, and socially linked. On the other hand, they consist of a heterogeneous combination of plant species with different uses that should be considered in multiple-use management. The importance of plant communities is usually evaluated using three ecological, economic, and social aspects (Baskent 2018). In economics, ecosystems are valuable because human well-being is affected by their functions. Basically, the philosophical basis of valuation is humanism. According to this approach, the nature components are valuable as long as they somehow benefit humans. Utilitarianism is one of the humanist theories that the value of nature's functions is to the extent that it brings satisfaction to man (Rudolf et al. 2002). Numerous studies have examined plant species value in ecology, human societies, and economics (Reyes-García 2001; Kakudidi 2004; Gokhale et al. 2011). For example, García-Llorente et al. (2012) used monetary and non-monetary techniques to explore the relationship between landscape multi-functionality and social preferences in semi-arid ecosystem, or Zabala et al (2021) presented a novel economic valuation of services in agroecosystem. However, the value of species composition in plant communities has received little attention. Managers face many uncertainties such as the plant communities’ dynamics. An important characteristic of ecological systems such as rangelands is that they consist of several different states (Walker et al. 1981). State and transition model illustrates the distribution and dynamics of plant communities and can help to predict the plant communities' response to environmental and management factors (Stringham et al. 2003). Under non-equilibrium model, plant communities are dynamic and transform into each other due to environmental disturbances (Tipton et al. 2018). The state and transition model reveals known and unknown features of an ecosystem that can be used for describing and restoring ecosystem (Heady and Child 1999), being very useful for arid ecosystems management (Bestelmeyer et al. 2017).
Although the concept of multiple-use management is receiving growing attention, the complexity of multiple-use management is increased due to the presence of diverse uses in ecosystems (Baskent 2018). This study examines the value of plant species based on three ecological, economic, and social aspects. Then plant communities are determined, and the value of plant communities under different uses is estimated through their plant composition. Therefore, providing a template for multiple-use management is an important part of rangeland management. The objectives of this study are (1) ecological, social, and economic valuation of plant species, (2) evaluation of the spatial distribution of plant communities and determining their value along landscape, (3) investigating the relationship between plant communities and different utilization types, and (4) designing a state and transition model based on change in plant communities’ value under different management.
Materials and methods
Research site
The study was conducted in Esfandaqeh rural district, Jiroft County, Kerman Province, south east of Iran (56° 56′ to 57° 18′ E and 28° 39 to 28 52 N). Mean annual rainfall is about 200 mm. Rangeland is the main land use in the region. There are different vegetation types in the region, varying from Pistacia atlantica woodland in upstreams to Artemisa aucheri shrublands in downstreams.
Rangelands comprise approximately 90 million ha of Iran. They provide 6% of the gross national product and are the main source of income for many poor, rural residents (Farahpour 2002). They provide food and income for about 180,000 pastoral families, and about 1.4 million families depend indirectly on rangeland (FAO 2006). Rangelands are a common resource, and exploitation is allowed via the use of permits, and thus land tenure is public. Rangelands are traditionally exploited by two types of ranchers (individual and group).
Sampling approach and procedure
Plant communities were valued using the value of their species. Value of plant species is divided into three categories of ecological, social, and economic values (Sarukhán and Whyte 2005). Ecological value of species was measured based on field data and the importance of species in plant communities (Mandal and Joshi 2014). The social and economic values of species were estimated based on people's perception on species value in the social system in which the number of uses was selected as the social value (Reyes-García et al. 2006) and the contribution of plant species to household income was considered as the economic value (Reyes-García 2001; Reyes-García et al. 2006).
The vegetation survey was carried out using 192 nested quadrats of different sizes located in three sites to show the variability of plant species composition across studied landscape. In each site, 10 × 10 m quadrats were used to sample trees and shrubs and 1 × 1 m sub-quadrats were used to sample semi-shrubs and herbaceous plants. In each quadrat, plant species richness and canopy cover were measured and Shannon diversity index was then calculated. Furthermore, the intensity of different uses (e.g., grazing, fruit collecting, wood harvesting, plants collecting (edible and medicinal), and beekeeping) was qualitatively determined for each quadrat in five classes ranging from very high to very low.
For social and ecological valuations, fifteen locals were first interviewed to get familiar with the plant species they use and their local uses. They were asked to list the name of all the useful plants they knew and their uses. Second, 86 locals were chosen for interview using stratified sampling method. The average age of participants was 46, and 63% were females and 37% were males. They were asked “do you know this plant?”, “do you use it for food, medicine, firewood, construction, dye, tools, aesthetic, forage, or beekeeping?”. To determine economic value of species, we asked each adult present in the household to report the name of all the plants that they had brought to the household.
Data analysis
Ecological, social, and economic values of plant species
The ecological value (EcVe) or Importance Value Index (IVI) of plant species was determined using their frequency, density, and dominance as follows (Curtis and McIntosh, 1951; Mishra, 1968):
where
Social value of plant species was calculated as follows:
where \({\text{SV}}_{e}\) is the social value of plant species e. \({\text{Uc}}_{e}\) is the total number of uses reported for plant species e divided by the nine potential uses for species considered in this study (i.e., food, medicine, firewood, construction, dye, tools, aesthetic, forage, and beekeeping). \({\text{IUc}}_{e}\) is the number of respondents who mentioned each use of the plant species e divided by the total number of respondents (Reyes-García et al. 2006).
Economic value of plant species was calculated as follows:
where EVe is the economic value of plant species e. Oee is the number of respondents who had income for buying each use of species divided by the total number of respondents, Pee is the price of each use the plant species, and Pemax is maximum price of species (Reyes-García et al. 2006).
Total value of plant species
As importance of ecological, social, and economic values of species is not the same for each species, analytic hierarchy process (AHP) was used to weight these values. Specifically, 12 ecological and economic experts were asked to express how two different criteria or alternatives are compared to each other in terms of their importance (Saaty 1980). The pairwise comparisons in a judgment matrix have been adequately consistent if the corresponding consistency ratio (CR) is less than 10%. Total value of plant species (TVe) was calculated as follows:
where W1, W2, and W3 are relative weights of ecological, social, and economic values of plant species, respectively.
Value of plant communities
Value of plant communities (PCV) was measured using the abundance of their plant species (Ae) and total value (TVe) of species as follows:
State and transition model
Changes in plant communities under different uses were displayed using the state and transition model. Plant communities or states were identified using clustering methods, and the relationship of plant communities with different uses (transition) was estimated using ordination method and the important uses in each state.
Plant communities
Two Way INdicator SPecies ANalysis (TWINSPAN, Hill 1979) was used to determine the distribution of plant communities as different states across landscape. Vegetation data were classified by two-way index species analysis, which is a hierarchical clustering method that uses differential species to describe and distinguish plant classes (McCune and Mefford 1999). In this study, plant communities resulted from TWINSPAN were considered as states of model.
Relationships between plant communities and different uses
Non-metric multidimensional scaling (NMDS) ordination procedure with the Bray–Curtis dissimilarity index is the most generally effective ordination method for determining drivers of ecological communities (McCune and Grace 2002). NMDS is an ordination method that displays a multidimensional dissimilarity matrix of data in a low-dimensional space. Less dissimilarity between data causes them to be closer to the NMDS space (Helm et al. 2017). NMDS was applied to reveal the relationship of plant communities with different uses. Pearson’s correlation coefficients were used to assess the relationships between plant community value with diversity, richness, and different uses in plant community. One-way analysis of variance (ANOVA) followed by the least significant difference (LSD) tests was used to compare different growth forms in terms of ecological, social, and economic values. Furthermore, different exploitation patterns (solitary and group) of plant communities were determined and compared in terms of ecological, social, economic, and total value of plant species using independent t-test.
Results and discussion
Results
A total of 82 plant species in 28 families were observed in sampling plots (Table S1). There were substantial variations between different plant species in terms of ecological, social, and economic values (Table 1). Amygdalus scoparia (SV = 8.51), Amygdalus wendelboi (SV = 7.56), and Pistacia atlantica (SV = 5.7) had the highest social value in the region, respectively. The highest ecological values belonged to Artemisia aucheri (IVI = 0.113), Astragalus gossypinus (IVI = 0.090), and Amygdalus wendelboi (IVI = 0.060). Pistacia khinjuk (EV = 93), Pistacia atlantica (EV = 86), and Juniperus polycarpos (EV = 81) and Acer monspessulanum subsp. persicum (EV = 36) had the highest social value, respectively. Ecological, social, and economic values of species were estimated based on AHP (Table S2).
Comparison of different growth forms in terms of ecological, social, and economic values showed that shrubs and trees had the highest importance in terms of ecological and social values, and trees had the highest importance in terms of economic value (Table 2, Fig. 1).
TWINSPAN analysis resulted in 17 different plant communities (Fig. 2) which considered as states. Ecological, social, and economic values of different communities were estimated using plant species values and their abundance in each community (Table 3). Plant community dominated with Thymus lancifolius and Lolium perenne (total value = 8.513) and plant community dominated with Peganum harmala and Salsola kali (total value = 0.001) had the highest and lowest total value between 17 considered plant communities in the region. The intensity of different uses is shown in Table 4 (grazing, edible or medicinal plants collecting, fruits collecting, wood harvesting, and beekeeping). The highest grazing intensity was related to states 1, 3, and 4. States 13 and 14 were the most exploited ones in terms of plants collecting. The highest intensity of fruit collecting was observed in states 13 and 17. States 9 and 17 had the highest intensity of wood harvesting. States 10 and 12 had the highest intensities in terms of beekeeping.
Figure 3 shows the distribution of 17 states with regard to 5 different uses (grazing, plants collecting, fruits collecting, wood harvesting, and beekeeping). There were significant relationships between different uses and states 10, 12, 6, 5, 15, and 14. The highest association was observed between states 2, 7, and 17; wood harvesting, states 3, 9, and 13 and fruit collecting, states 1, 4, and 8 and livestock grazing, and states 11 and plant harvesting and beekeeping. Pearson's correlation coefficients showed that there was a significant relationship between the value of plant communities and Shannon's diversity, richness, and the multiple uses in plant community (Fig. 4).
The plant communities with solitary exploitation had greater ecological, social, economic values compared to group exploitation (Fig. 5).
The state and transition model of region rangelands represents the changes in the value of states due to different uses (Fig. 6). The vertical axis represents the relative total value of the states estimated according to value of their plant species. The horizontal axis shows the relative number of uses in each state. In this model, the change of states under the dominant use as the transition is separately displayed in each landscape. In mountain semi-shrubland, state 10 transits to states 11, 12, and 13, during which only the value of state 12 has not passed the threshold value and the other two states are substantially changed. In mountain forest, state 15 transits to states 11 and 16, both of which have exceeded the threshold of plant communities’ value. In mountain shrubland, state 6 changes to states 7, 8, and 9, among which state 9 had the highest loss of value. In plain semi-shrubland, stable state 5 also shifts to states 3 and 4, during which the value of plant communities decreases, although the changes are less intense than other plant communities.
Discussion
In the most landscapes, plant communities are not distributed evenly and may have different ecological, economic, and social values. Therefore, each plant community has a certain potential for different uses depending on its vegetation composition. Plant communities have experienced different types of degradation based on their dominant use. Such plant communities, which are faced to uneven disturbances, may need to be spot managed (Fuhlendorf and Smeins 1999), so that their management should be consistent with the distribution of anthropogenic disturbances (Fuhlendorf and Engle 2001).
Previous studies on the impact of solitary and group exploitations on rangelands condition and people income have shown that group exploitation is one of the continuous actions to alleviate poverty and have mentioned the solitary exploitation as the cause of adverse effects on rangelands (Maggs and Hoddinott 1999; Adhikari et al. 2004). In this study, however, the two types of exploitation (solitary and group) also had different effects on the condition of plant communities. In the highlands where the variety of landscape uses was higher, the status of solitary exploited rangelands was better than the group exploited rangelands. In the lowlands, where the rangeland uses were less diverse and the dominant use is livestock grazing, the status of group exploited rangelands was better than the solitary exploited rangelands. Solitary exploitation was the best in landscapes rich in plant species because of fewer exploiters, better comprehensive management, and less competition for exploiting.
Plant communities’ diversity and their value
We have found that species diversity enhances the value of plant communities through increasing multiple use of landscapes. Former studies indicated that biodiversity has a positive impact on ecosystem functions and consequently ecosystem multiple use (e.g., Mace et al. 2012; Balvanera et al. 2006; Worm et al. 2006; Quijas et al. 2010; Cardinale et al. 2012). In areas where species richness is higher, the number of uses from plant communities is higher and has higher value. The cost of value loss due to exploitation in these communities is higher than those areas where the number of uses is limited.
All plant species contribute to ecosystem functioning, but their values are not the same for ecosystems and social systems (Kakudidi 2004). Sometimes, a key species alone can significantly enhance the value of plant communities (Quijas et al. 2012), and removal of such species can severely decrease the value of plant communities. Although Pistacia atlantica forests are not very diverse in species, they are of great value because of the presence of valuable species Pistacia atlantica in this community. Pistacia atlantica is one of the economic trees that grows in the Mediterranean regions (Bozorgi et al. 2013). In addition to providing forage for livestock and wild animals, and production edible seeds and gum, this species is valuable in terms of genetic reservoir, natural attractions, ecotourism, soil and water conservation, and flood control (Bozorgi et al. 2013; Mahjoub et al. 2018). Fruit of this species has been traditionally used as medicine and food (Razavi 2005). This plant is an important source of gum that is used in pharmaceutical and industrial applications (Sharifi and Hazell 2011). Wild almond (Amygdalus scoparia) alone has promoted the value of plant communities. Wild almond fruits are a source of nutrients and oils that are of great importance for human health and food (Abbey et al. 1994). Wild almond flowers appear in late winter to early spring before the plant leaf emergence, giving a very beautiful view of the tree, which are important for attracting honeybees and producing honey.
Different uses and plant communities
As well as heterogeneity of plant communities, diversity of uses may face ecosystem managers with more challenges. Multiple uses were differently declined plant communities value and created new states. Based on suggested state and transition model, plants collecting and wood harvesting had more negative impacts on the plant communities’ value compared to grazing. In the upstream shrublands, plants collecting and grazing decreased the plant communities’ value by 71% and 44%, respectively, and wood harvesting and grazing decreased communities’ values by 85% and 59%, respectively, in Pistacia atlantica woodlands. Conversely, wood harvesting and grazing decreased the value of downstream shrub communities by 56% and 85%, respectively, through low ecological, social, and economic values of shrub species Daphne stapfii. Therefore, impact of grazing on plant communities’ value is reduced by increasing the number of uses in plant communities.
Our results showed that there was a synergy relationship between medium grazing, plant collecting, and fruit collecting in communities with the highest value. Wild edible plants are of great importance to human societies by providing food for humans and animals and generating extra income sources for locals. The importance of edible plant species is growing day by day due to their health benefits and others advantages (Garcia-Herrera et al. 2014). Diet selection of livestock depends on the quality and composition of plant communities (Rook et al. 2004; Dumont et al. 2007). When the plant community is rich in aromatic and medicinal plants, the livestock usually tend to go for the more nutrient species (van Braeckel and Bokdam 2002). In upstream shrublands, livestock prefer palatable grasses such as Lolium perenne, causing its removal from plant community in state 12. But this community still has an acceptable value because grasses are just used as forage and have lower economic and social value. On the other hand, valuable medicinal and edible plants in this community (such as Thymus lancifolius, Ziziphora clinopodioides, Bunium persicum) generally contain essential oils, and livestock are not attracted to them compared to Lolium perenne and annual legumes.
However, over-collecting of edible and medicinal plants has greatly reduced the value of upstream shrub communities. So the intensity of plants collecting had a greater impact on the value of plant communities compared to overgrazing in upstream.
Multiple-use management and different plant communities
Multiple-use management is difficult to implement because all uses must be adapted with landscape potential to providing multiple functions (Maxwell et al. 2019). Planners and decision makers must combine all uses to enhance complementary relationships and minimize competitive interactions between different uses (McGranahan and Kirkman 2013). States that are in acceptable condition in the region (e.g., states of 6, 10, 12, and 15), are a good guide to maintain the value of plant communities along with their sustainable use. Based on states 10 and 12, ecosystems with solitary exploitation are of the highest value because there is less competition between people for exploiting. On the other hand, light grazing increases plants growth and vitality through removing old and dead parts of plants (Noy-Meir 1993), providing a better condition for plants growth and consequently their exploitation. Since grazed grasses and forbs are also not collected by people, there is no trade-off between grazing and plants collecting in states 10 and 12 located in upstream. However, in downstream where plant diversity is low and multiple uses are limited, medium grazing intensity had the least negative impact on the value of Artemisia aucheri plant communities under group exploitation. Shrubs such as Artemisia aucheri are forage plants that have a greater contribution to ecological, social, and economic values in downstream. Therefore, if the grazing intensity is severe, ecosystems will be more damaged. In plant communities where key species play an important role in community (e.g., states 6 and 15), management should be primarily focused on their conservation.
Management strategies are needed to restore degraded states (e.g., 1, 2, 3, 4, 7, 8, 9) and to return them to acceptable previous states. Although plants collecting plays an important role in the livelihood of locals (Karabak 2017), it should be reduced in states such as 11 and 13. Therefore, the goal of ecosystem management must be in order to conserve medicinal and edible species, as this is the way to maximize long-term economic and social benefits. Since many of these edible and medicinal plants are traded locally, it is very important to commercialize these products for international markets (e.g., for pharmacological purposes) to improve revenue of local people (Karabak 2017). Decreasing grazing pressure can cause the system to restore to stability in overgrazed states (Bestelmeyer et al. 2004), while restoration dynamics is facilitated by local abiotic conditions such as elevation, rainfall, soil texture (Lopez et al. 2013; Tietjen 2016). Upstream communities due to receiving higher rainfall can be restored by decreasing grazing intensity, but it is not enough for downstream areas where environmental condition is harsh; therefore, biological rehabilitation is needed. The results suggest that trees and shrubs are key species that have higher social, economic, and ecological values than other species and can be used to restore states with lowest value (e.g., states 1 and 4).
Conclusion
This study provided a new method to facilitate the management of ecosystems with multiple and intense uses. The combined social, economic, and ecological values of plant communities provide an appropriate indicator to show changes of plant communities under different management plans. The state and transition model simplified the complexities of multi-functional ecosystem with uneven managements. States with the highest community value, where intensity of multiple uses is adjusted to ecosystem potential and there are synergy between multiple uses, are priorities for regional conservation. States with lowest community value are critical areas where the intensity of adverse uses must be minimized. Our finding can provide important information for sustainable management of complex arid ecosystems.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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AKM involved in conducting of interview and preparing questionnaires, fieldwork, filling questionnaires, general data collection, and writing the manuscript. All authors wrote, read, and approved the final manuscript. MS involved in the study design, laboratory work, fieldwork, filling questionnaires and general data collection, and writing the manuscript. SN involved in preparing questionnaires, economic evaluation, and writing the manuscript.
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All experimental protocols were approved by Review Board of Faculty of Natural Resources, University of Jiroft, Iran. All methods were carried out in accordance with relevant guidelines and regulations. Informed consent was obtained from all participants.
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Khosravi Mashizi, A., Sharafatmandrad, M. & Naghavi, S. Ecosystems multiple-use management: an approach based on change in economic, social, and ecological values of plant communities. Int. J. Environ. Sci. Technol. 19, 3845–3858 (2022). https://doi.org/10.1007/s13762-021-03513-w
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DOI: https://doi.org/10.1007/s13762-021-03513-w