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Riparian and wetland ecosystems throughout the southwestern United States are being threatened by the invasion of tamarisk (Tamarix spp.), a non-native woody shrub introduced from Eurasia in the 1800s1. Tamarisk has many physiological mechanisms that allow the genus to exploit water resources, out-compete native species, and alter ecosystem processes1-2. Mapping tamarisk distributions for assessing environmental impacts and formulating effective control strategies are high priorities for resource managers. Although ground surveys remain regularly used, they are impractical for extremely large areas due to the associated costs of labor, time, and logistics.
Satellite remote sensing has played an important, but limited, role in the detection and mapping of tamarisk infestations. Conventional classification analyses and remote sensing software have had marginal success3-5. Several recent studies have explored non-traditional approaches to detect invasive plants using remote sensing data1,6. Tamarisk, like many invasive plants, exhibits phenological variation throughout the growing season that differs from native riparian species' phenology. In some areas, for example, tamarisk leaf-out is before some native riparian plants, and tamarisk retains its foliage longer than other native species. By using spectral bands and spectral indices derived from a time-series of satellite data throughout the growing season, we can distinguish tamarisk from native plants based on these phenological differences1,6. Building on the work of Evangelista et al. 20091, in this study we incorporated individual bands 1-7 from a time-series of Landsat 5 Thematic Mapper (TM) satellite imagery and derived normalized difference vegetation index (NDVI), soil-adjusted vegetation index (SAVI), and tasseled cap transformations from these bands. Normalized difference vegetation index (NDVI) is one of the most commonly used spectral indices for estimating vegetation biomass, canopy cover, and leaf area indices8-9, and is a non-linear transformation of the ratio between the visible (red) and near-infrared bands10. Soil-adjusted vegetation index (SAVI) is a modified NDVI used to minimize the effects of soil background on vegetation indices11. Tasseled cap transformations are weighted composites of the six Landsat bands into three orthogonal bands that measure soil brightness (tasseled cap, band 1), vegetation greenness (tasseled cap, band 2), and soil/vegetation wetness (tasseled cap, band 3) and are often used to distinguish vegetation composition, age class, and structure12-14. We used the coefficients reported in Crist (1985)15 for all tasseled cap transformations.
In this study, we test five species distribution models with a time-series of spectral bands and vegetation indices derived from Landsat 5 TM to map tamarisk along the lower Arkansas River in southeastern Colorado, USA. The Arkansas River, spanning 2,364 km (1,469 mi), is the second largest tributary in the Missouri-Mississippi system. Its watershed covers 435,123 km2 (168,002 mi2) with headwaters in the Colorado Rocky Mountains. From its origin at 2,965 m, the Arkansas drops considerably in elevation, leveling out near Pueblo, CO, and meandering through agricultural lands and short-grass prairie. The river is subject to seasonal flooding and is relied on for municipal and agricultural water use in Rocky Ford, La Junta, and Lamar, before continuing into Kansas, Oklahoma, and Arkansas where it flows into the Mississippi River. Tamarisk was first observed on the Arkansas River by R. Niedrach in 1913 near the present-day town of Lamar16. Today, it has been estimated that tamarisk covers more than 100 km2 between Pueblo and the Kansas state line, with an additional 60 km2 along the tributaries of the Arkansas River17. The study area includes irrigation ditches, wetlands, agricultural land, and the confluences of several tributaries; all with varying degrees of tamarisk infestation. Ranching and agriculture are the primary land-uses adjacent to the riparian corridors consisting largely of alfalfa, hay, corn, and winter wheat.
Species distribution models rely on geo-referenced occurrences (i.e., latitude, longitude) to identify relationships between a species' occurrence and its environment18. The environmental data can include multiple remote sensing and other spatial layers. The five species distribution models we tested include boosted regression trees (BRT)19, random forests (RF)20, multivariate adaptive regression splines (MARS)21, a generalized linear model (GLM)22, and Maxent23. These five model algorithms are among the most commonly employed for species distribution modeling, and a number of studies have demonstrated their efficacy24-25. We used the Software for Assisted Habitat Modeling (SAHM) v. 2.0 modules to execute the five models, which are contained in VisTrails v.2.2.226 visualization and processing software. There are several advantages to using SAHM for comparative modeling. In addition to the formalization and tractable recording of modeling processes, SAHM allows users to work with multiple species distribution model algorithms that, individually, have disparate interfaces, software and file formatting27. SAHM produces consistent threshold-independent and threshold-dependent evaluation metrics to evaluate model performance. One of these is Area Under the Receiver Operating Characteristic Curve (AUC), a threshold independent metric that evaluates ability of a model to discriminate presence from background28. An AUC value of 0.5 or less indicates model predictions are not better or worse than random; values between 0.5 and 0.70 indicate poor performance; and values increasing from 0.70 to 1.0 indicate progressively higher performance. Another metric is percent correctly classified (PCC), a threshold dependent metric that weighs sensitivity and specificity based on a user-defined threshold metric; sensitivity measures the percentage of observed presences classified as suitable and specificity measures the percentage of background locations classified as unsuitable. Yet another metric is True Skill Statistic (TSS = sensitivity + specificity - 1), which places more weight on model sensitivity than specificity, with values ranging between -1 and 1 where values > 0 indicate better model performance than chance29.
To map tamarisk using model output, we constructed binary classifications using the threshold that equalizes sensitivity and specificity to define the presence or absence of tamarisk. These individual model derived maps were then summed to create an ensemble map30. Ensemble maps combine the predictions of individual species distribution models to produce a classified map that ranks the collective agreement of the models tested. For example, an ensemble cell value of one indicates that only one model classified that cell as suitable habitat, whereas a value of five indicates that all five models classified the cell as suitable habitat. One advantage to this approach is that ensemble maps yield a lower mean error than any individual model. It also allows users to visually compare the performance of each model tested. Our overall goal was to provide a detailed description of these methods that can be tailored to model the current distribution of species on the landscape.