Abstract
The development of spatially differentiated management strategies against invasive alien plant species requires a detailed understanding of their current distribution and of the level of invasion across the invaded range. The objectives of this study were to estimate the current fractional cover gradient of invasive trees of the genus Prosopis in the Afar Region, Ethiopia, and to identify drivers of its invasion. We used seventeen explanatory variables describing Landsat 8 image reflectance, topography, climate and landscape structures to model the current cover of Prosopis across the invaded range using the random forest (RF) algorithm. Validation of the RF algorithm confirmed high model performance with an accuracy of 92% and a Kappa-coefficient of 0.8. We found that, within 35 years after its introduction, Prosopis has invaded approximately 1.17 million ha at different cover levels in the Afar Region (12.3% of the surface). Normalized difference vegetation index (NDVI) and elevation showed the highest explanatory power among the 17 variables, in terms of both the invader’s overall distribution as well as areas with high cover. Villages and linear landscape structures (rivers and roads) were found to be more important drivers of future Prosopis invasion than environmental variables, such as climate and topography, suggesting that Prosopis is likely to continue spreading and increasing in abundance in the case study area if left uncontrolled. We discuss how information on the fractional cover and the drivers of invasion can help in developing spatially-explicit management recommendations against a target invasive plant species.
Similar content being viewed by others
Introduction
Invasive alien plant species (IAPS) are key drivers of anthropogenic global environmental change as they threaten native species, communities and ecosystems1, with significant consequences for the people living in the invaded range2,3. Yet, the management of widely established IAPS is often complex and challenging, as eradication is not feasible. Rather, management strategies may need to integrate multiple management options across the invaded range, considering the current geographic distribution and abundance of the target species, its environmental niche in the invaded region, the areas within the invaded range that are likely to experience high impacts, the distribution of high-value areas that should be kept free from invasion and the availability of funding for management4,5,6. Moreover, two classes of factors also affect management of IAPS: (i) intrinsic biological factors, such as the reproductive mode and the number of propagules produced7, and (ii) extrinsic environmental factors, such as dispersal vectors and invasion pathways8. Ignoring these factors may make the spatial management of IAPS challenging and complicated.
As management options may differ between areas with high IAPS cover and those areas where only isolated patches are found, accurate and detailed information is needed on the actual area invaded as well as on the local abundance or cover of IAPS across the invaded region. In recent years, an increasing number of papers have been published providing distribution maps of IAPS at different spatial scales and with different resolution9. One way to address this issue is to develop fractional cover maps of IAPS, but such mapping products of invasive species have rarely been developed10. Fractional vegetation cover assessments, mostly in semi-arid environments, were so far mainly a methodological research focus of the remote sensing research community. Machine learning algorithms, such as Random Forest (RF) in combination with satellite data, show the potential to model tree biomass successfully and accurately11 or to map a variety of vegetation covers12. Besides providing accurate predictions, they are able to model complex interactions among input variables, to identify most significant explanatory variables13,14, and to handle noise or outliers15. An approach with such advantages could possibly also be suitable for developing fractional cover maps as well as help identifying the relative importance of factors in explaining the current and predicting the future distribution and abundance of IAPS13,14, thereby providing important information for developing spatially explicit management strategies.
During the 19th and 20th century, various species and hybrids of the genus Prosopis that are native to South and Central America were planted in areas outside their native range (e.g. Australia, southern Asia, southern and eastern Africa) with the aim of providing firewood, charcoal, fodder and timber, to stabilize soil in degraded ecosystems, and prevent desertification16. The first introductions in Ethiopia were made during the 1970s and 1980s17,18, but problems arose soon thereafter, in the early 1990s, when the tree started invading croplands, grasslands, riverbanks and roadsides, thereby causing significant environmental impacts19, and becoming a source of conflict among pastoralist groups due to the resulting dwindling grazing land20. Despite its potential benefits, particularly regarding the provision of firewood and charcoal, Ethiopia has declared Prosopis a noxious weed and has recently published a national Prosopis management strategy21. In the case of Prosopis, various distribution maps have been developed with the goal to describe the spatial extent of Prosopis invasion22,23, its spread over time23,24, or model its potential invasion area25. However, all of these studies either focused on relatively small study areas or if they were extensive provided only coarse-resolution maps of either presence or absence of the species.
In this study, we set out to create a fractional cover map of Prosopis for the Afar Region, Ethiopia, one of the areas in Eastern Africa most heavily invaded by Prosopis. Most introductions in Ethiopia were made with Prosopis juliflora (Sw.) DC20, but as the taxonomic status of the invasive trees across study region has yet to be confirmed, we refer to the target species hereafter as Prosopis. The specific objectives of the study were (i) to assess the current distribution and cover of Prosopis invasion in the Afar Region by applying a robust machine learning algorithm (the random forest modelling) based on a large number of field data on local cover, and (ii) to identify factors that explain the current distribution of Prosopis along a cover gradient and drivers of future Prosopis invasion in the Afar Region. Specifically, we aimed to assess whether a) combining image spectral reflectance and environmental variables results in a better performance of the Prosopis distribution model than either group of variables alone, b) the overall distribution of Prosopis and the distribution of highly invaded areas is explained by the same or different variables, and whether c) landscape structures such as watercourses or road networks and environmental variables are suitable as predictors of future Prosopis invasion. Based on our findings, we outline approaches for using fractional cover maps and what they reveal about an invasion process to design and prioritize Prosopis management in this dryland ecosystem.
Materials and Methods
Study area
The study was carried out in the Afar Region, Ethiopia, which is part of the Great Rift Valley of East Africa. The study area extends from 8.8°N to 14.5°N and 39.7°E to 42.4°E, covers an area of 9.51 million ha and includes five zones, 30 districts and 376 kebeles (the lowest administrative units in Ethiopia; Fig. 1). The Afar Region has a mean annual rainfall of about 560 mm while the estimated mean evapotranspiration is 2,200 mm per year26. The region is the hottest part of Ethiopia, and the mean annual temperature is 31 °C. The mean maximum temperature reaches 41 °C in June and July, and the mean minimum temperature ranges from 21 to 22 °C between November to January. The mean monthly minimum and maximum rainfall recorded for the period 1965–1999 is 3 mm (June) and 121 mm (August), respectively, and the mean annual relative humidity ranges from 38 to 58 percent26. The major watershed in the Region is the Awash River Basin. Most parts of Afar Region are characterized by patches of scattered dry shrubs, acacia woodland, bushland, grassland and wooded grassland27.
The Afar people depend on the floodplains of Awash River for grazing during the drought periods and for small-scale agriculture28. Pastoralism is still the dominant source of livelihood for the Afar people, but agro-pastoralism is promoted by the government. In addition, governmental and private investments have led to large-scale agricultural production in the Middle Awash Valley, particularly in cotton and sugar cane production. Also, parts of the arable land have been abandoned as a result of soil salinity, which resulted from both inappropriate irrigation practices and high evapotranspiration of Prosopis invasion28.
Study species
The genus Prosopis belongs to the family Fabaceae, subfamily Mimosoideae. It includes about 45 species, mainly found in the arid and semi-arid regions of the world29. Prosopis trees are able to fix nitrogen and have deep root systems, rendering them resistant to droughts. Several different species had been introduced into Eastern Africa and hybridization among parental species has been documented16.
According to Kebede and Coppock20, Prosopis was first introduced and planted in Ethiopia in the late 1970s at a nursery in West Harerghe and subsequently transplanted into the Afdem and Afar areas (Amibera and Gewane districts) in the early 1980s. Additional plantations were made between the 1980s and 1990s20 as shade trees in villages, around crop fields or to reduce erosion in degraded areas23. The locations of the original plantations reported by local key informants are compiled and shown in Figure 1.
Sampling design and datasets
Georeferenced field data were collected throughout the entire study area using a stratified random sampling approach. Presence and absence plots were purposively selected from invaded and uninvaded areas, respectively. Invaded areas were additionally stratified into areas likely to be highly invaded (around villages, along roads, on riverbanks) and areas likely to be less invaded (outside villages, away from roads and riverbanks). The sampling plots were randomly selected within the different strata and substrata. In order to reduce spatial autocorrelation, sampling plots were selected that had a minimum separation distance of 500 m30. A total of 2,722 field sample plots of 20 m by 20 m (presence and absence plots) were collected between September 2016 and March 2017. A plot was considered a presence plot if it contained at least one Prosopis plant; otherwise it was considered an absence plot. About 70% (n = 1922) of the samples were absence plots and about 30% (n = 800) were presence plots. These proportions approximately correspond to the proportions of uninvaded and invaded land in the study area to avoid any bias of results towards either absence or presence of Prosopis31,32. Each geo-referenced sampling plot was recorded together with its level of Prosopis coverage, which was estimated visually to the nearest 10%. About 80% of all sampling plots were randomly selected to be used for model calibration and the remaining 20% were used for validation33.
The spatial datasets (17 independent variables) that we used to explain Prosopis distribution were gathered from various sources (Table 1). They differed in terms of spatial resolution34, projection, and time of acquisition; nearest neighbor spatial resampling and reprojection was applied to obtain a common spatial pixel resolution of 15 m. The field plots and the ancillary datasets (explanatory variables) had relatively equivalent pixel size35. Spatial resampling was done to match the dataset with the highest spatial resolution, the panchromatic band of the Landsat 8 Operational Land Imager (OLI) data was used in this study. In total, nine scenes were needed to cover the study area. They were acquired by the Landsat 8 (OLI) on 26 and 28 January as well as 11 and 20 February 2017 (paths: 167 and 168; rows: 50 to 54). These acquisition dates match the period of field data collection and fall into the study area’s dry season, when herbs and grasses are dry and most trees and bushes except Prosopis have shed their leaves. The remotely sensed datasets were visually checked for geometric correspondence to all other datasets. Further, these datasets were atmospherically corrected using the Landsat Ecosystem Disturbance Adaptive Processing System (LEDAPS) algorithm36. We selected the red, the near-infrared and the first shortwave-infrared bands as explanatory variables among image reflectance37. Furthermore, we calculated the normalized difference vegetation index (NDVI), which is a ratio of the difference between the near-infrared and the red band to the sum of the near-infrared and the red band of a specific sensor. All selected bands as well as the NDVI have proven suitable for capturing photosynthetic active vegetation, and soil and vegetation moisture content37. Additionally, we included two products of the MODIS sensor in our analysis, daytime (LSTd) and nighttime (LSTn) land surface temperatures. In order to have longer term LSTd and LSTn average data we calculated 5-year averages from the monthly LSTd and LSTn products that were generated between 2012 and 2017. The spatial resolution of these data is 1 km. Although this seems rather low compared to the other datasets, these day- and night-time temperature datasets have been shown to be useful in species distribution modelling38. We furthermore sought to understand if day- and night-time temperatures are important explanatory or drivers of Prosopis distribution. Additionally, we used variables representing topography, infrastructure, and watercourses. These variables have been previously shown to influence distribution of invasive species39,40.
Random forest modeling
To regress and assess fractional cover and distribution of Prosopis in the Afar Region, we used Random Forest (RF), a nonparametric technique based on classification and regression trees (CART)13. RF consists of an arbitrary number of trees, where each tree is generated by bootstrap samples. About one third of the overall sample is left for validation (the out-of-bag predictions – OOB). Each split of the tree is determined using a randomized subset of the predictors at each node. The final outcome is the average of the results of all the trees13,14. The number of decision trees was found to be optimal if set to 5,000 trees. The number of features was set to the square root of the number of input variables, as has been done in another study41. We carefully checked that the out-of-bag error was stable with the chosen settings before applying the model. We assessed the model performance by calculating its accuracy, Kappa coefficient, correlation, and the Receiver Operating Characteristics (ROC) of area under the curve (AUC). It is a prevalence- and threshold independent measure of model performance suitable for evaluating the performance of ordinal score models42. Moreover, we calculated sensitivity (true positive rate - TPR) and specificity (true negative rate - TNR) of the model43.
We applied a 10-fold validation approach, i.e. repeating the validation in ten different calibration batches and comparing the outcome with that of the training data for each of these batches44. We then calculated the threshold value for presence and absence of Prosopis31,39. This approach identified the minimum area where Prosopis trees occur whilst ensuring that no localities at which the species has been observed are omitted, i.e. omission rate of the minimum39 with a certain precision obtained from the model.
Factors explaining the current distribution of Prosopis
To achieve greater stability of the models, we first assessed the importance of variables in each model by using the method described by Natekin and Knoll45. We then removed variables from the final models if they contributed less than 5% to the model (Appendix 1). To assess the importance of the various sets of explanatory variables in explaining the overall distribution of Prosopis and the distribution of areas with increasing Prosopis cover (i.e. areas with potentially increasing environmental impacts), we set two types of iterations. Iteration (i) used three scenarios with different sets of explanatory variables: scenario 1 included all image spectral reflectance and environmental variables (Appendix 1); scenario 2 included spectral reflectance variables only, and scenario 3 included environmental variables only. Iteration (ii) used scenario 1 but with four different threshold levels of presence input cover estimations, i.e. at ≥5%, ≥20%, ≥40%, and ≥60%.
We used a weighted mean fitted analyses approach46 to explore the main environmental correlates of the current Prosopis distribution and cover40,46,47,48. This approach provides more consistent information on the shape of the fitted surface than what can be obtained from individual functions with respect to the species distributions49.
Drivers of Prosopis invasion
To identify the main drivers of the invasion of Prosopis, we determined the relative importance of input variables. As the use of multivariate regression requires standardization (centering and scaling) to identify each variable’s influence on species distribution50,51, we standardized the variables by subtracting means from each corresponding value of the driver, and dividing the center value by the standard deviation51. In the interpretation of potential drivers of Prosopis invasion, we excluded the spectral variables NDVI, NIR and SWIR that all respond to vegetation photosynthetic activity, since this spectral response can be considered both as cause and effect of Prosopis presence.
Statistical analyses
All model calculations and validations were implemented in the open source R software version 3.3.3, while mapping of outputs were carried out using ESRI ArcGIS. The RF modelling was implemented in R using the randomForest52 and boosted regression tree (brt) packages53. The relative importance of the explanatory variables was estimated using the Friedman formulae54,55 which is contained the gbm package47. Moreover, the contribution and direction of importance of each variable were evaluated by analyzing their marginal effect curves and fitting polynomial smoothing47,48. Finally, the fractional cover gradient of the RF model output was matched with the ground invasion level by correlating the threshold levels of presences and absence.
Results
Extent of invasion for the current distribution of Prosopis
The area invaded by Prosopis in the Afar Region is estimated to be about 1,173,000 ha (12.3% of the total regional area; Fig. 2, Appendix 2). Validation of the model performance revealed an accuracy of 92% and a Kappa coefficient of 0.8 at P < 0.001 (Table 1). In addition, sensitivity and specificity evaluations were 0.894 and 0.926, respectively, and AUC, correlation and threshold measures were also high (Appendix 1). The model output threshold was identified as 0.326, which corresponds to the minimum starting cover level of ~0.004% of Prosopis presence map at 15 m pixel size.
By 2017, four of the five zones and 21 of the 30 districts in the Afar Region were invaded by Prosopis (Fig. 2A; Appendix 2). Prosopis distribution was the highest in Zone 3 (Gabi Rasu), with 193,920 ha in Gewane district (22% invaded) to 74,972 ha in Bure Mudaytu (68% of area invaded; Fig. 2B, Appendix 2). Districts with high mean cover were identified from different zones: in Zone 3 Amibara District (32%), in Zone 5 Artuma District (24%), in Zone 4 Teru District (23%) and in Zone 1 Aysaita District (23%). Only 9 districts were found to be almost free of Prosopis, i.e. Berahle, Erebti, Megale, Afdera, Dalul and Abala districts in Zone 2, Argoba Special and Koneba districts in Zone 3, and Gulina District in Zone 4. By 2017, all of these districts had less than 1.3% of their area invaded by Prosopis (Appendix 2).
Explanatory variables for the current distribution of Prosopis
Both the selection of explanatory variables and input threshold levels of visual estimated cover affected model performances. Among the three tested scenarios, scenario 1 generated the highest performance relative to scenarios 2 (using image reflectance variables only) and 3 (using environmental variables only; Fig. 3). NDVI, Elevation and NIR were the three most important variables for scenario 1 (Fig. 3A). In scenario 2, SWIR, NIR, NDVI were ranked highest, and in scenario 3 Elevation, LSTn, and Rainfall (Appendix 1).
Shifting the input threshold levels for Prosopis cover in scenario 1 from ≥5% to ≥60% had only moderate effects on the ranking of the explanatory variables. NDVI revealed the highest relative importance independent of the input threshold, followed by Elevation, DistVillage and DistRiver. The only consistent change with increasing input threshold for Prosopis cover was an increasing relative importance of DistRoad (Fig. 3).
Individual explanatory variables differed in terms of the spatial range of interaction with the dependent variable, Prosopis presence. DistVillage affected Prosopis presence up to a distance of 10 km, while DistRiver and DistRoad mainly affected Prosopis presence over a distance of a few hundred to thousand meters (Fig. 4). Environmental correlates of Prosopis distribution and cover are indicated by the magnitude and direction of weighted mean fitted values of each explanatory variable in relation to the response variable (fractional cover). Important environmental correlates of the current Prosopis distribution and cover were DistRivers, DistRoads and DistVillage, with average values of distances up to 5913 m, 2679 m and 1937 m, respectively (Appendix 3). Prosopis is currently preferentially found at an altitude of below 1000 m (average 585 m asl) and an mean annual temperature of 20–29 °C (average 24.4 °C). Annual rainfall of 200–1000 mm (average 608 mm) was most conducive for the current distribution and cover of Prosopis, but some invaded areas experience less than 200 mm rainfall (Fig. 4).
Partial dependency or marginal effect curve indicating overall importance of 16 variables for explaining Prosopis (the number in brackets next to each variable name is the proportion of Prosopis fractional cover explained by that variable in final model) (y-axis for all plots are fitted values, but x-axis are different units).
Drivers of Prosopis invasion
The three landscape variables DistRiver, DistRoad, and DistVillage were the most important drivers of local Prosopis invasion (Fig. 5). In contrast to their role in explaining the current distribution of Prosopis, climatic variables appear to be only moderately important drivers and image reflectance variables are to be the least important drivers of invasion.
Discussions
Extent of invasion for the current distribution of Prosopis
Within approximately 35 years, Prosopis has invaded about 12.3% of the land in the Afar Region of Ethiopia. It is most widespread in the southern parts of the Afar Region, especially in Zone 3. In the areas where the original plantations had been made, Prosopis has already invaded an average of up to 31% of the district’s area in Amibara (with 32% cover abundance) and about 68% of the land was invaded in Bure Mudaytu District (with 30% cover abundance). The southern part of the Afar Region is not only the point of introduction of Prosopis but it has also experienced many economic activities over the last four to five decades34 that could contribute to spread of the tree. For instance, large government-owned investments, private farms, and populations of pastoralists, and agro-pastoralists are found in the southern part of the Region23. Hence, habitat disturbance due to land-use changes23 may further explain why Prosopis invasion is more pronounced in the southern than the northern parts of the Afar Region.
In contrast to previous studies25, our fractional cover map indicates large areas in the Afar Region with low Prosopis densities, and some of these areas are relatively far away from the original plantations. This suggests that Prosopis invasion in the Afar Region is likely to continue increasing over the next decades if no measures to manage this invasive species are implemented.
Explanatory variables for the current distribution of Prosopis
By combining Landsat 8 image reflectance variables with variables describing the topography, climate and landscape structure of the Afar Region (scenario 1), we achieved approximately 92% accuracy for modelling the fractional cover of Prosopis across the invaded range. Modelling the cover of Prosopis using either image reflectance variables only or environmental variables only resulted in a lower accuracy, suggesting that the integration of image reflectance and environmental variables was responsible for the highest accuracy of the model used for mapping the fractional cover of Prosopis in Afar Region. Other studies developing invasive plant species distribution models also found that adding generic variables such as climate, land use and disturbance increased the accuracy of the models1,30.
Our results suggest that Prosopis started to spread from multiple focal points (original plantation sites, villages, etc.) and subsequently invaded the surroundings along linear corridors (river courses, travel routes) that act as dispersal pathways. Linear landscape characteristics have been repeatedly shown to explain IAPS distributions56,57. Bartuszevige57 found that towns as focal points were also of primary importance in explaining the distribution of the invasive shrub Lonicera maackii in the eastern U.S.A., and secondary invasion of L. mackii to suitable habitats was mediated through birds. Similarly, invasion of Prosopis into areas away from DistVillages, DistRivers or DistRoads appears to occur at a lower cover, but the role of additional factors affecting the current distribution or cover of Prosopis, such as migration corridors of livestock and wildlife, warrant further investigations as they could be used as ‘jump dispersal’ agents58.
In an attempt to explore the relative importance of factors of invasions of three woody IAPS in South Africa, Rouget and Richardson59 found that geology, climate, land use, and topography adequately explained distribution of these species, while cover was better explained by propagule pressure, measured as distance from putative invasion foci. Considering that variables such as DistVillage, DistRiver and DistRoad can also be interpreted as indicators of dispersal pathways, the highest ranking of DistRiver and DistVillage in the models with and without reflectance data suggest that propagule pressure plays an important role in explaining both the current distribution and cover of Prosopis in the Afar Region.
The importance of DistRoad and DistRiver on Prosopis invasion extended up to 10 km at both sides in a non-linear relationship. However, in most parts of the study area, the highest invasion of Prosopis occurred within a strip of ten to a few hundred m along roadsides and riverbanks. Similarly, Flory and Clay60 showed that densities of three invasive species had higher germination rates than natives in USA, declined with increasing distance to the nearest road, and the percent cover of exotic species was significantly greater at 10 and 100 m from roads than at 1000 m from roads61.
Partial dependency or marginal effect curve indicated that NDVI had the highest contribution to explain the current distribution of Prosopis in the arid ecosystems (Fig. 4) because it is an effect of invasion46. Moreover, weighted fitted mean values of independent variables (Appendix 3) elucidate the importance of interactions between predictors and identify the optimal habitats of species49. It should be noted, however, that areas with high Prosopis cover are usually areas that were colonized first (Shiferaw et al., unpubl.), suggesting that large areas currently with low cover will increase in cover within the next decades.
Drivers of Prosopis invasion
Decision tree-based regressions such as RF have been recently proposed for predicting invasion processes of IAPS8,62,63. For example, Menuz and Kettenring8 found that climate variables were most important for predicting invasive plant species distributions across the large study area and factors related to nutrients, land cover, and disturbance had only moderate importance. Starting with a climate model and then nesting models with additional landscape, land use and structural predictors, Vicente et al.64 explored a range of different drivers of plant invasions in Portugal. They found that climate was the most important driver, while other landscape variables contributed where climate was favourable.
Our study suggests that, among the variables included in the analysis, river courses, road networks and village vicinities are the most important drivers of Prosopis invasion in the Afar Region (Fig. 5). River courses, particularly during flooding events, are known to serve as modes of transportation of Prosopis pods and seeds to downstream areas, a process termed ‘corridor dispersal’58. Besides transportation, seeds of Prosopis transported by river-courses also benefit from increased moisture that allows them to germinate and grow quickly. Similarly, ditches along road-networks maintain moisture longer than the surrounding ecosystems, thereby offering Prosopis ideal conditions for germination and early growth (Shiferaw, personal observation). In particular, our findings suggest that the invasion of the riparian habitats along the Awash River will continue downstream, thereby accelerating the loss of drought-season grazing areas and also aggravates associated conflicts among pastoralist communities65.
While invasion of Prosopis into areas away from villages, rivers or roads appears to occur at a lower rate, the role of additional factors driving invasion by Prosopis, such as migration corridors of livestock and wildlife, warrant further investigations. Pods of Prosopis have sugary flesh and contain several seeds which makes them important food sources of both wild and domestic animals during the long dry season26. Animals regurgitate, scratch or break hard seed coats, and scratched seeds germinate and grow faster than intact seeds, due to increased moisture imbibition and dung acting as manure26.
In contrast to Menuz and Kettenring8 and Vicente et al.64, our data suggest that precipitation and elevation, which are climatic variables describing the environmental niche of plant species35, are less significant drivers of future Prosopis invasion than are landscape structure variables, at the current stage of invasion. This supports our previous notion that a considerable part of environmentally suitable habitats in the Afar Region have not yet been fully colonized by Prosopis and that this plant invader is therefore likely to continue spreading and increasing in abundance if left uncontrolled.
Fractional cover approach
Fractional cover mapping is a relatively recent approach to combine both information on the overall distribution and the variation in abundance or cover of an alien species in the invaded range. Fractional cover maps provide key information regarding the overall impact of IAPS, as they provide information on the overall invaded area and on local abundance66. As with many other invasive plant species, the impact of Prosopis on biodiversity and ecosystem processes has been shown to be abundance- or cover-dependent67.
Fractional cover maps have only rarely been used to assess the current distribution of IAPS and their abundance across the invaded range. Frazier and Wang10 assessed the spatial and local status of saltcedar (Tamarix spp.) invasion in parts of the invaded range in North America, and they suggested that saltcedar had originally invaded the region along river-courses but subsequently expanded away from the immediate riparian zones. They concluded that targeting isolated saltcedar stands from the riparian zone should be part of an integral saltcedar management strategy in the region.
Our approach to model the fractional cover of Prosopis in the Afar Region achieved an accuracy of 92% (with an AUC of 0.97), which is higher than accuracies achieved in most other species modelling approaches25,68. This is in agreement with previous studies, suggesting that RF is a suitable algorithm for species distribution modelling8 and fractional cover mapping14. Moreover, fractional cover mapping approach also allowed identification of isolated, small patches of Prosopis in the Afar Region, which are main targets for management (see below subheading). In this study, we converted the modelled probability maps into fractional Prosopis cover maps by setting the threshold of uninvaded areas to 0.326. We used the maximum intersection of sensitivity and specificity as threshold31,39,48.
We suggest that five points should be considered in order to achieve good results while applying RF regression: (1) sufficient and well-distributed field data samples should be collected in the study area; (2) the number of presence and absence field samples should be proportional to the overall proportions of sites in the study area where the species is present and absent, respectively; and (3) the field data values for the dependent variable should be within the range of the expected prediction values, (4) as shown by previous study, the values of explanatory variables used for training need to represent the entire range of values present in the study area69, and (5) variable reduction and fine-tuning of selected parameters can improve the model fitness and regression outputs.
Fractional cover map and invasive species management
Understanding the extent of the current distribution and abundance of IAPS and predicting future invasion pathways are crucial for scientists and decision-makers who wish to quantify the regional impacts of IAPS and to design management strategies that help reducing the current cover levels and the further spread of IAPS35,58. As eradication is usually not possible for widespread IAPS, spatially explicit management strategies should be developed that assign different control objectives (prevention of spread to unoccupied areas, local eradication, containment and asset protection) to areas with different invasion level6,70,71. Recently, Ethiopia adopted a National Strategy on Prosopis juliflora management21. The strategy includes three main objectives: (i) prevent the expansion of Prosopis to uninvaded areas; (ii) reclaim and restore invaded areas after Prosopis clearance; and (iii) sustainably manage of Prosopis for productive use and increasing biodiversity through regulation and coordination of Prosopis management initiatives21.
Our Prosopis fractional cover map provides essential information for implementing an early detection and rapid response system, which is primarily targeted at areas with low Prosopis cover and at neighboring uninvaded areas. Prevention of permanent establishment of IAPS in uninvaded areas is a key component of most invasive species strategies67 as it is the most cost-effective means to prevent losses of ecosystem services due to ecosystem degradation72,73. Based on our findings, surveillance of uninvaded areas should particularly focus on buffer zones of approx. 10–100 m along roadsides and riverbanks, but may need to be extended to other linear structures such as livestock migration routes. If Prosopis is found within the buffer zones along linear structures, the area should be further surveyed up to one kilometer away from the linear structures (Fig. 4). Emphasis should also be put at targeting and managing isolated Prosopis patches since satellite populations of IAPS may play a key role in the future spread of IAPS1,73,74. The high resolution and accuracy rate of our Prosopis fractional cover map helped identifying numerous spots in the Afar Region where satellite trees or patches of Prosopis occur.
Moreover, the fractional cover map also helped identifying high-value areas that are at risk of invasion by Prosopis. For example, areas of nature reserves bordering Prosopis invaded rangeland should be monitored and young plants continuously removed. In regions where Prosopis occurs in the surroundings of protected areas and livestock is allowed to enter these areas, as it is currently the case for Awash National Park, measures may be needed to fence livestock away from Prosopis prior to entering the protected areas to prevent establishment of new satellite stands from defecated seeds which remain viable after gut passage75.
The rate of spread of Prosopis in the Afar Region and the strong indication that this species has not yet filled its environmental niche in the region call for consideration of a sustainable long-term management of this aggressive invader, also in remote areas. Experiences made with woody IAPS management suggest that a combination of biological control reducing reproductive output and physical control removing established trees is among the most promising and sustainable strategies, if not the only one, to reduce cover of dominant invasive tree species22,72. In Australia, the release of a biological control agent, the leaf-tying moth Evippe sp. (Lepidoptera: Gelechiidae), has resulted in very low growth and fertility rates of Prosopis76.
Conclusions
Using Prosopis invasion in the Afar Region, Ethiopia, as a model system, our study suggests that the RF regression can help producing accurate fractional cover maps of IAPS that help explaining their current distribution and abundance as well as predicting future invasion patterns. The incorporation of environmental variables significantly improved the accuracy of the model and revealed that landscape structure variables, such as distance to rivers, road and villages, were more significant drivers of Prosopis distribution than climatic variables, suggesting that Prosopis is likely to continue spreading and increasing in abundance in the case study area if left uncontrolled. The knowledge gained does not only generate basic knowledge on IAPS invasion processes, it also provides support for the development and implementation of spatially explicit management strategies that may include different management interventions in different parts of the invaded range, and with different priorities. In particular, because of the high accuracy of our model, achieved partly through extensive sampling of field data, our approach allowed identification of numerous areas with low Prosopis cover, i.e. areas with early invasion stages that should be targeted for rapid response (removal of isolated patches at the invasion front) to prevent further spread of this IAPS in the case study region. We propose that the establishment and interpretation of fractional cover maps of IAPS should become a key component of IAPS management at the regional or national scale.
References
Vilà, M. et al. Ecological impacts of invasive alien plants: a meta-analysis of their effects on species, communities and ecosystems. Ecol. Lett. 14, 702–708 (2011).
Pejchar, L. & Mooney, H. A. Invasive species, ecosystem services and human well-being. Trends Ecol. Evol. 24, 497–504 (2009).
Pimentel, D., Zuniga, R. & Morrison, D. Update on the environmental and economic costs associated with alien-invasive species in the United States. Ecol. Econ. 52, 273–288 (2005).
Le Maitre, D. C., Gush, M. B. & Dzikiti, S. Impacts of invading alien plant species on water flows at stand and catchment scales. AoB Plants 7 (2015).
Woodford, D. J. et al. Confronting the wicked problem of managing biological invasions. NeoBiota 31, 63–86 (2016).
Shackleton, R. T., Le Maitre, D. C., Van Wilgen, B. W. & Richardson, D. M. Towards a national strategy to optimise the management of a widespread invasive tree (Prosopis species; mesquite) in South Africa. Ecosyst. Serv. 1–11 https://doi.org/10.1016/j.ecoser.2016.11.022 (2017).
Lockwood, J. L., Blackburn, T. M., Cassey, P. & Olden, J. D. The shape of things to come: non-native mammalian predators and the fate of island bird diversity. Holocene Extinctions 235 (2009).
Menuz, D. R. & Kettenring, K. M. The importance of roads, nutrients, and climate for invasive plant establishment in riparian areas in the northwestern United States. Biol. Invasions 15, 1601–1612 (2013).
Zimmermann, N. E., Edwards, T. C., Graham, C. H., Pearman, P. B. & Svenning, J. C. New trends in species distribution modelling. Ecography (Cop.). 33, 985–989 (2010).
Frazier, A. E. & Wang, L. Characterizing spatial patterns of invasive species using sub-pixel classifications. Remote Sens. Environ. 115, 1997–2007 (2011).
Karlson, M. et al. Mapping tree canopy cover and aboveground biomass in Sudano-Sahelian woodlands using Landsat 8 and random forest. Remote Sens. 7, 10017–10041 (2015).
Lorena, A. C. et al. Comparing machine learning classifiers in potential distribution modelling. Expert Syst. Appl. 38, 5268–5275 (2011).
Breiman, L. Random forest 2001. 1–33, https://doi.org/10.1017/CBO9781107415324.004 (2001).
Cutler, D. R. et al. Random Forests for Classification in Ecology. Ecology 88, 2783–2792 (2007).
Rodriguez-galiano, V. F., Rogan, J. & Rigol-sanchez, J. P. An assessment of the effectiveness of a random forest classifier for land-cover classification. ISPRS J. Photogramm. Remote Sens. 67, 93–104 (2012).
Pasiecznik, N. M. The Prosopis juliflora - Prosopis pallida Complex: The Prosopis juliflora - Prosopis pallida Complex (2001).
Sertse, D. & Pasiecznik, N. M. Controlling the Spread of Prosopis in Ethiopia by its Utilization. HDRA. Hdra (2005).
Mwangi, E. & Swallow, B. Invasion of {{Prosopis juliflora} and local livelihoods}. World Agrofor. Cent. 68, https://doi.org/10.4103/0972-4923.49207 (2005).
Shackleton, R. T., Le Maitre, D. C., Pasiecznik, N. M. & Richardson, D. M. Prosopis: A global assessment of the biogeography, benefits, impacts and management of one of the world’s worst woody invasive plant taxa. AoB Plants 6, 1–18 (2014).
Kebede, A. T. & Coppock, D. L. Livestock-Mediated Dispersal of Prosopis juliflora Imperils Grasslands and the Endangered Grevy’s Zebra in Northeastern Ethiopia. Rangel. Ecol. Manag. 68, 402–407 (2015).
National Prosopis Management Strategy. Ministry of Livestock and Fisheries (2017).
Van Wingen, B. W. et al. An assessment of the effectiveness of a large, national-scale invasive alien plant control strategy in South Africa Brian W. Van Wilgen. Biol. Conserv. 148, 28–38 (2012).
Ayanu, Y. et al. Ecosystem engineer unleashed: Prosopis juliflora threatening ecosystem services? Reg. Environ. Chang. 15, 155–167 (2014).
Robinson, T. P., Van Klinken, R. D. & Metternicht, G. Spatial and temporal rates and patterns of mesquite (Prosopis species) invasion in Western Australia. J. Arid Environ. 72, 175–188 (2008).
Wakie, T. T., Evangelista, P. H., Jarnevich, C. S. & Laituri, M. Mapping current and potential distribution of non-native prosopis juliflorain the Afar region of Ethiopia. PLoS One 9, 3–11 (2014).
Shiferaw, H., Teketay, D., Nemomissa, S. & Assefa, F. Some biological characteristics that foster the invasion of Prosopis juliflora (Sw.) DC. at Middle Awash Rift Valley Area, north-eastern Ethiopia. J. Arid Environ. 58, 135–154 (2004).
Engda, G., Sensing, R. & Systems, G. I. Spatial and Temporal Analysis of Prosopis juliflora (Swarz) DC Invasion in Amibara woreda of the Afar NRS Spatial and Temporal Analysis of Prosopis juliflora (Swarz) DC Invasion in Amibara Woreda of the Afar NRS (2009).
Argaw, T. Impacts of Utilizing Invasive Prosopis juliflora (SWARTZ) DC. on Rural Household Economy at Gewane District, Afar Regional. J. Econ. Sustain. Dev. 6, 81–98 (2015).
Pasiecznik, N. M., Harris, P. J. C. & Smith, S. J. Identifying Tropical Prosopis Species A Field Guide. Managing 44 (2004).
Cabra-Rivas, I., Saldaña, A., Castro-Díez, P. & Gallien, L. A multi-scale approach to identify invasion drivers and invaders’ future dynamics. Biol. Invasions 18, 411–426 (2016).
Jiménez-Valverde, A. & Lobo, J. M. Threshold criteria for conversion of probability of species presence to either-or presence-absence. Acta Oecologica 31, 361–369 (2007).
Rodríguez, J. P., Brotons, L., Bustamante, J. & Seoane, J. The application of predictive modelling of species distribution to biodiversity conservation. Divers. Distrib. 13, 243–251 (2007).
Meynard, C. N. & Quinn, J. F. Predicting species distributions: A critical comparison of the most common statistical models using artificial species. J. Biogeogr. 34, 1455–1469 (2007).
Rettberg, S. Contested narratives of pastoral vulnerability and risk in Ethiopia’s Afar region. Pastoralism 1, 248–273 (2010).
Guisan, A. & Thuiller, W. Predicting species distribution: Offering more than simple habitat models. Ecol. Lett. 8, 993–1009 (2005).
Lu, D., Mausel, P., Brondizio, E. & Moran, E. International Journal of Assessment of atmospheric correction methods for Landsat TM data applicable to Amazon basin LBA. Int. J. Remote Sens. 23, 2651–2671 (2002).
Barsi, J. A., Lee, K., Kvaran, G., Markham, B. L. & Pedelty, J. A. The spectral response of the Landsat-8 operational land imager. Remote Sens. 6, 10232–10251 (2014).
He, K. S. et al. Will remote sensing shape the next generation of species distribution models? Remote Sens. Ecol. Conserv. 1, 4–18 (2015).
Pearson, R. G. Species’ distribution modeling for conservation educators and practitioners. Lessons Conserv. 3, 54–89 (2010).
Elith, J. et al. A statistical explanation of MaxEnt for ecologists. Divers. Distrib. 17, 43–57 (2011).
Belgiu, M. & Drăgu, L. Random forest in remote sensing: A review of applications and future directions. ISPRS J. Photogramm. Remote Sens. 114, 24–31 (2016).
Metz, C. E. Basic principles of ROC analysis. Semin. Nucl. Med. 8, 283–298 (1978).
Liaw, A. & Wiener, M. Classification and Regression by randomForest. R news 2, 18–22 (2002).
Chen, L., Peng, S. & Yang, B. Predicting alien herb invasion with machine learning models: biogeographical and life-history traits both matter. Biol. Invasions 17, 2187–2198 (2015).
Natekin, A. & Knoll, A. Gradient boosting machines, a tutorial. Front. Neurorobot. 7, (2013).
Leathwick, J. R., Elith, J., Chadderton, W. L., Rowe, D. & Hastie, T. Dispersal, disturbance and the contrasting biogeographies of New Zealand’s diadromous and non-diadromous fish species. J. Biogeogr. 35, 1481–1497 (2008).
Elith, J., Leathwick, J. R. & Hastie, T. A. working guide to boosted regression trees - Online Appendices Page 1. J. Anim. Ecol. 77, 802–813 (2008).
Hijmans, R. J. & Elith, J. Species distribution modeling with R. R CRAN Proj. 79 pp, https://doi.org/10.1016/S0550-3213(02)00216-X (2015).
Hijmans, R. J. & Elith, J. Species distribution modeling with R Introduction (2016).
Araújo, M. B. & Guisan, A. Five (or so) challenges for species distribution modelling. J. Biogeogr. 33, 1677–1688 (2006).
Craig, A., Cloarec, O., Holmes, E., Nicholson, J. K. & Lindon, J. C. Scaling and normalization effects in NMR spectroscopic metabonomic data sets. Anal. Chem. 78, 2262–2267 (2006).
Breiman, L. Random forests. Mach. Learn. 45, 5–32 (2001).
Elith, J., Leathwick, J. R., Hastie, T. & R. Leathwick, J. Elith, Leathwick & Hastie A working guide to boosted regression trees - Online Appendices Page 1. J. Anim. Ecol. 77, 802–813 (2008).
Ridgeway, G. Generalized Boosted Models: A guide to the gbm package. Compute 1, 1–12 (2007).
Elith, J. & Graham, H. C. Do they? How do they? WHY do they differ? On finding reasons for differing performances of species distribution models. Ecography (Cop.). 32, 66–77 (2009).
Rouget, M. & Richardson, D. M. Inferring process from pattern in plant invasions: a semimechanistic model incorporating propagule pressure and environmental factors. Am. Nat. 162, 713–724 (2003).
Bartuszevige, A. M. et al. Nordic Society Oikos The relative importance of landscape and community features in the invasion of an exotic shrub in a fragmented la. Ecography 29, 213–222 (2006).
Wilson, J. R. U., Dormontt, E. E., Prentis, P. J., Lowe, A. J. & Richardson, D. M. Something in the way you move: dispersal pathways affect invasion success. Trends Ecol. Evol. 24, 136–144 (2009).
Rouget, M. et al. Mapping the potential ranges of major plant invaders in South Africa, Lesotho and Swaziland using climatic suitability. Divers. Distrib. 10, 475–484 (2004).
Flory, S. L. & Clay, K. Effects of roads and forest successional age on experimental plant invasions. Biol. Conserv. 142, 2531–2537 (2009).
Gelbard, J. L. & Harrison, S. Roadless habitats as refuges for native grasslands: Interactions with soil, aspect, and grazing. Ecol. Appl. 13, 404–415 (2003).
Mcshane, R. R. et al. Distribution of invasive and native riparian woody plants across the western USA in relation to climate, river flow, floodplain geometry and patterns of introduction. Ecography (Cop.). 38, 1254–1265 (2015).
Mainali, K. P. et al. Projecting future expansion of invasive species: Comparing and improving methodologies for species distribution modeling. Glob. Chang. Biol. 21, 4464–4480 (2015).
Vicente, J., Alves, P., Randin, C., Guisan, A. & Honrado, J. What drives invasibility? A multi-model inference test and spatial modelling of alien plant species richness patterns in northern Portugal. Ecography (Cop.). 33, 1081–1092 (2010).
Stark, J. & Terasawa, K. Climate Change and Conflict in Pastoralist Regions of Ethiopia: Mounting Challenges, Emerging Responses, https://doi.org/10.1186/2193-7532-1-13 (2011).
Parker, I. M. et al. Toward a framework for understanding the ecological effects of invader. Biol. Invasions 1, 3–19 (1999).
Shackleton, R. T., Le Maitre, D. C., Van Wilgen, B. W. & Richardson, D. M. The impact of invasive alien Prosopis species (mesquite) on native plants in different environments in South Africa. South African J. Bot. 97, 25–31 (2015).
Stockwell, D. R. B. & Peterson, A. T. Effects of sample size on accuracy of species distribution models 148, 1–13 (2002).
Hengl, T. et al. Mapping soil properties of Africa at 250 m resolution: Random forests significantly improve current predictions. PLoS One 10, 1–17 (2015).
Grice, A. C., Clarkson, J. R. & Calvert, M. Geographic differentiation of management objectives for invasive species: A case study of Hymenachne amplexicaulis in Australia. Environ. Sci. Policy 14, 986–997 (2011).
Terblanche, C. et al. An approach to the development of a national strategy for controlling invasive alien plant species: The case of Parthenium hysterophorus in South Africa. Bothalia 46(1), a2053, https://doi.org/10.4102/abc.v46i1.2053 (2016).
Coutts, S. R., Van Klinken, R. D., Yokomizo, H. & Buckley, Y. M. What are the key drivers of spread in invasive plants: Dispersal, demography or landscape: And how can we use this knowledge to aid management? Biol. Invasions 13, 1649–1661 (2011).
Caplat, P., Hui, C., Maxwell, B. D. & Peltzer, D. A. Cross-scale management strategies for optimal control of trees invading from source plantations. Biol. Invasions 16, 677–690 (2014).
Vilà, M. & Ibáñez, I. Plant invasions in the landscape. Landsc. Ecol. 26, 461–472 (2011).
Haregeweyn, N., Tsunekawa, A., Tsubo, M., Meshesha, D. & Melkie, A. Analysis of the invasion rate, impacts and control measures of Prosopis juliflora: A case study of Amibara District, Eastern Ethiopia. Environ. Monit. Assess. 185, 7527–7542 (2013).
Robinson, T. P., Van Klinken, R. D. & Metternicht, G. Comparison of alternative strategies for invasive species distribution modeling. Ecol. Modell. 221, 2261–2269 (2010).
Acknowledgements
We are grateful for financial support from the Swiss Programme for Research on Global Issues for Development (r4d), funded by the Swiss National Science Foundation (SNSF) and the Swiss Agency for Development and Cooperation (SDC), for the project “Woody invasive alien species in East Africa: Assessing and mitigating their negative impact on ecosystem services and rural livelihood” (Grant Number: 400440_152085). Urs Schaffner was supported by CABI with core financial support from its member countries (see http://www.cabi.org/about-cabi/who-we-work-with/key-donors/). We thank the staff of Addis Ababa University’s Water and Land Resource Center for their support and facilitation services, and Sanford Eigenbrode for critically reviewing the manuscript.
Author information
Authors and Affiliations
Contributions
All authors designed the study. HS collected the field data, developed and ran the model. H.S., U.S. and S.E. wrote the draft. And all authors edited the paper.
Corresponding author
Ethics declarations
Competing Interests
The authors declare no competing interests.
Additional information
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Shiferaw, H., Schaffner, U., Bewket, W. et al. Modelling the current fractional cover of an invasive alien plant and drivers of its invasion in a dryland ecosystem. Sci Rep 9, 1576 (2019). https://doi.org/10.1038/s41598-018-36587-7
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-018-36587-7
- Springer Nature Limited
This article is cited by
-
Experimental prosopis management practices and grassland restoration in three Eastern African countries
CABI Agriculture and Bioscience (2023)
-
Diversity and abundance of birds in dumpsites of Afar region, Ethiopia: implication for conservation
BMC Zoology (2023)
-
Utilising random forests in the modelling of Eragrostis curvula presence and absence in an Australian grassland system
Scientific Reports (2023)
-
Statistically optimized charcoal production from Prosopis juliflora for use as alternative fuel in cement factories
Biomass Conversion and Biorefinery (2023)
-
Species Distribution Modelling performance and its implication for Sentinel-2-based prediction of invasive Prosopis juliflora in lower Awash River basin, Ethiopia
Ecological Processes (2021)