Abstract
The duration of inundation or saturation (i.e., hydroperiod) controls many wetland functions. In particular, it is a key determinant of whether a wetland will provide suitable breeding habitat for amphibians and other taxa that often have specific hydrologic requirements. Yet, scientists and land managers often are challenged by a lack of sufficient monitoring data to enable the understanding of the wetting and drying dynamics of small depressional wetlands. In this study, we present and evaluate an approach to predict daily inundation dynamics using a large wetland water-level dataset and a random forest algorithm. We relied on predictor variables that described characteristics of basin morphology of each wetland and atmospheric water budget estimates over various antecedent periods. These predictor variables were derived from datasets available over the conterminous United States making this approach potentially extendable to other locations. Model performance was evaluated using two metrics, median hydroperiod and the proportion of correctly classified days. We found that models performed well overall with a median balanced accuracy of 83% on validation data. Median hydroperiod was predicted most accurately for wetlands that were infrequently inundated and least accurate for permanent wetlands. The proportion of inundated days was predicted most accurately in permanent wetlands (99%) followed by frequently inundated wetlands (98%) and infrequently inundated wetlands (93%). This modeling approach provided accurate estimates of inundation and could be useful in other depressional wetlands where the primary water flux occurs with the atmosphere and basin morphology is a critical control on wetland inundation and hydroperiods.
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Introduction
Small isolated wetlands are important landscape features that provide myriad ecosystem services (Cohen et al. 2016). They are known hotspots for nutrient and chemical transformation (Reddy and DeLaune 2008), sequester disproportionately large quantities of carbon relative to their area (Mitsch and Gosselink 2015; Marton et al. 2015; Craft et al. 2018), and harbor an abundance of threatened and endangered species (Williams and Dodd Jr 1978; Murdock 1995; Smith et al. 2019). However, the key attribute influencing a wetland’s function, water permanence or inundation duration (i.e., hydroperiod), is rarely known or quantified. In this study, we define hydroperiod as the duration of consecutive days with ponded surface water. In regard to amphibians, hydroperiod has been shown to be a far stronger determinant of taxa richness than wetland size (Snodgrass et al. 2000; Babbitt et al. 2003; Babbitt 2005), and many amphibian species will only breed in temporary wetlands (Dodd 1992, 1993). Thus, knowledge of hydroperiod is key to protecting critical habitat and preserving biodiversity of wetland obligate species. Furthermore, the lack of knowledge on water permanence or connections to permanent waterbodies has led to shifting legal protections for various surface water features including geographically isolated wetlands (e.g., McLaughlin et al. 2014; Cohen et al. 2016; Rains et al. 2016). Even with these uncertainties we are unaware of any widespread efforts to better monitor and assess water permanence in small wetlands beyond localized scales (e.g., NCDWR, 2018). This lack of hydrologic information can lead to land and species management decisions that might ignore a critical piece of information. Hence, tools are needed to help predict water permanence (hydroperiod) in small, isolated wetlands where data often are lacking, and the small size of which precludes the use of most currently available (and free of cost) remotely sensed data.
Past efforts to predict wetland hydrology have been based on three broad categories of techniques: physically based process models, remote sensing approaches, and empirical models. Physically based process models have been used to simulate the complex hydrology of pine flatwoods pre- and post-forest harvest (Sun et al. 1998, 2007) and to more broadly examine the role of forest harvest and management on wetland hydrology in low relief landscapes (Skaggs et al. 2005). Other studies have used these models to investigate potential impacts on wetland hydrology from climate change (Kurki-Fox et al. 2019) and to model hydrologic processes in various types of depressional wetlands (Krasnostein and Oldham 2004; Caldwell et al. 2007; Qi et al. 2019; Cartwright and Wolfe 2021). This type of model can be especially useful when information regarding hydrologic processes is needed in addition to simulations of particular hydrologic outputs. However, one of the challenges with many physically based process models is the relatively high and diverse data requirements, such as detailed soil characteristics and water table elevations over the model domain, which are rarely available.
Remotely sensed data have been used to infer the presence or absence of surface water in wetlands and time series of these remotely sensed data can then be used to estimate the duration of inundation (e.g., Jones 2019; Wu et al. 2019; Hopkinson et al. 2020; Alonso et al. 2020; Kissel et al. 2020; Londe et al. 2022). One product designed specifically for this purpose is the Dynamic Surface Water Extent (DSWE, Jones 2015; Jones 2019). This dataset is derived from Landsat and therefore has repeat scenes of 8–16 days (assuming cloud cover is minimal and multiple sensors are used). Given the 30 m resolution of Landsat, this dataset is most applicable to larger wetland sites (i.e., those that are at least the area of several Landsat pixels). Other studies have coupled multiple sources of remote sensing data to backfill temporal gaps often present with a single satellite (Murray-Hudson et al. 2015; Wu et al. 2019). For example, in the prairie pothole region of the United States, Wu et al. (2019) combined aerial imagery and lidar data to explore wetland inundation dynamics. By combing these datasets, they were able to identify smaller waterbodies than were evident from satellite derived data alone and that provided a denser temporal record, which allowed more highly resolved estimates of inundated extent. While these examples of remote sensing approaches are highly viable in large, non-forested or sparsely forested wetland systems, they are often not practical for small, forested wetlands. This is especially true in humid regions that have frequent cloud cover, often limiting the consecutive satellite pass-overs that are suitable for analysis.
Empirical studies have used field data with statistical models to relate weather, climate, and characteristics of a wetland basin to the duration, depth, or area, of wetland inundation. Studies using these techniques have often focused more explicitly on hydroperiod determination than studies using physically based process models or remotely sensed data (e.g. Greenberg et al. 2015; Chandler et al. 2016; Kissel et al. 2020; Londe et al. 2022). For example, in a lowland coastal plain site Riley et al. (2017) showed that a neighborhood scale topographic metric was strongly related to wetland hydroperiod class (short, long, permanent), and in a nearby study site, Chandler et al. (2016) used generalized linear mixed models to predict water presence as a function of climatological and meteorological variables and wetland characteristics. Other studies have found climate indices (e.g., Palmer drought severity index, standardized precipitation index [SPI]) (Davis et al. 2019; Londe et al. 2022) as well as soil moisture (Kissel et al. 2020) to be important for prediction of wetland inundation. While statistical models have proven very useful for localized applications, predictors derived from field data often reflect site specific variables and may limit their transferability to different wetland sites. Collectively, however, the above studies suggest that empirical models should consider weather forcings and characteristics of the wetland basins for accurate inundation prediction.
The application of machine learning (ML) algorithms (another empirical modeling approach) to the broader domain of hydrologic prediction has greatly increased in the last decade (see Shen et al. 2021; Nearing et al. 2021; Zounemat-Kermani et al. 2021). Many studies that have used ML methods for hydrologic prediction have highlighted higher accuracy than physically based process and statistical models (e.g. Galeati 1990; Solomatine and Ostfeld 2008; Best et al. 2015; Nearing et al. 2016). Machine learning models, and specifically random forests, have many desirable properties for prediction problems: they are non-parametric (i.e., require no assumption regarding data distributions); they are not negatively affected by correlated predictors; and they can capture interactions between predictors, among others (see Tyralis et al. 2019). Despite the large body of literature that highlights accurate hydrologic predictions, we are only aware of a limited number of studies that have employed ML techniques for predicting wetland inundation dynamics (Shaeri Karimi et al. 2019; Choi et al. 2020; Cartwright et al. 2021; Solvik et al. 2021). Of these, only Cartwright et al. (2021) focused specifically on small depressional wetlands, and only Choi et al. (2020) attempted prediction at a daily time-step. The wetland community could benefit from additional studies using ML approaches to understand where they may be viable options for predicting inundation dynamics of small depressional wetlands.
The goal of this study was to explore a novel application of ML to predict daily inundation and estimate hydroperiods in small depressional wetlands. Specifically, we had three objectives: (1) build random forest models using widely available meteorological and elevation data to derive predictor variables to predict daily inundation and to estimate median hydroperiods; (2) assess model performance based on the proportion of days correctly classified and the accuracy the of median hydroperiods estimated from daily predictions; and (3) evaluate variable importance metrics to determine which predictors were most influential in classification accuracy. This will provide a framework for others to build and evaluate similar models to predict daily inundation where extensive field datasets for predictor variables may not exist.
Methods
Study Area and Hydrologic Data
This study was conducted using data from Saint Marks National Wildlife Refuge (SMNWR) in the Florida panhandle along the Gulf Coast (Fig. 1). Water levels were monitored in 59 wetlands that covered a variety of wetland types (cypress domes, flatwoods, wet prairies, hardwood wetlands, and sink-hole ponds), sizes (0.01 ha to 1.38 ha), and elevations (0.94 to 4.31 m, relative to North American Vertical Datum of 1988, Supplemental material table S1). Although some wetlands were at very low elevations, coastal flooding is rare in the study area and has mostly been associated with land falling tropical systems (Gunzburger et al. 2010). Specific monitoring periods in each wetland varied, but most had at least five years of record with a maximum of ten years. Monitoring equipment at each wetland consisted of a total pressure sensor (Hobo U-20, Onset Corporation, Cape Cod, MA) and staff gage installed in the deepest portion of the wetland’s basin, or in permanent wetlands, as deep as possible and in proximity to vegetation that indicated permanent inundation. To compensate for atmospheric pressure, a barometer was installed in a dry well below the water table. This was to prevent inaccuracies from large temperature swings that may occur when barometers are exposed to ambient air conditions (McLaughlin and Cohen 2011). All water level data were converted to a binary classification, where a mean daily water level ≤ 0.02 m was classified as “dry”; otherwise the wetland was considered inundated and classified as “wet.” This cutoff represents the average error observed when comparing water level from the pressure sensor to the staff gage readings. Furthermore, at a level of 0.02 m there will be little in the way of wetted habitat for aquatic and semi-aquatic organisms, in most cases rendering them “functionally dry.”
Datasets for Predictor Development
Daily precipitation depth, daily minimum and maximum air temperature, mean daily vapor pressure deficit (VPD), and daily reference evapotranspiration (PET) data were obtained from gridMET (Abatzoglou 2013), using the climateR R-package (Johnson 2021). Initial testing indicated that PET was a more important predictor than either of its components (air temperature or VPD), so these variables were removed from further consideration. The gridMET dataset provides daily meteorological data on an approximately 4-km2 grid across the contiguous United States. Given the relatively small study area extent, the grid cell at the centroid of the study area was used as the point to extract meteorological data.
Most of the monitored wetlands have been field mapped (Riley 2016) and those boundaries were used where available. Where boundaries were not field mapped, the national wetlands inventory (NWI) boundaries were used, and, where not present in the NWI, boundaries were heads-up digitized from the national aerial imagery program (NAIP) and a lidar derived digital elevation model (DEM). The dominant vegetation class for each wetland was extracted from the LANDFIRE (2016) dataset. The LANDFIRE dataset has a 30-m resolution and is not intended for high resolution vegetation mapping but can represent the vegetation class surrounding the wetlands. A lidar-derived 1-m DEM (FDEM 2008) was used to derive topographic metrics, including a topographic position index (TPI) (Weiss 2001; Jenness et al. 2011; Riley et al. 2017). In our study area an annulus shaped neighborhood with inner and outer radius of 20 and 40 cells, respectively, was used. All topographic metrics (mean TPI, mean elevation, and elevation range) were summarized within each wetland boundary.
Conceptualizing Wetland Hydrology for a Data Driven Model
The water budgets of the depressional wetlands in this study are primarily controlled by precipitation as the input and evapotranspiration (ET) as the output. Groundwater exchange certainly occurs but we lack data to adequately quantify that exchange. In similar wetlands, McLaughlin and Cohen (2012) found groundwater exchange frequently reversed directions between the wetlands and the surficial aquifer. Thus, the water budget is represented simply as ΔStorage = precipitation – potential evapotranspiration.
The differences are summed over various antecedent timesteps to represent different aspects of storage. Short lags (5–60 days) likely reflect storage conditions in the vadose zone and longer lags (60–180 days) may represent saturated zone storage conditions. Basin morphology (Fig. 2) along with antecedent storage conditions of soils, the surficial aquifer, and the wetland basin determines how a wetland will respond to precipitation and evapotranspiration. Wetlands with small surface areas but deep basins will collect relatively less precipitation but will also be less susceptible to evaporative losses as compared to broad shallow wetlands. To characterize wetland morphology, we used basin area for the 2-dimensional surface area and proxy variables, such as the TPI and elevation range, to represent the z-axis (depth) of wetlands. It is important to note, however, that TPI does not precisely represent the depth of the actual wetland but rather reflects the mean elevation of the wetland relative to the surrounding landscape. For example, a more negative TPI indicates a wetland is more deeply recessed in relation to the surrounding landscape compared to a wetland with less negative TPI. The TPI variable may also reflect the relative likelihood of a wetland intersecting the surficial aquifer and provides potential context for groundwater influence. Dominant vegetation type was also included which could be important for modulating the hydrologic response via interception and transpiration amongst the different types of wetlands (e.g., emergent vs. forested wetlands).
Model Description and Set-up
We used a random forest algorithm (Breiman 2001) implemented using R statistical software (R-Core Team 2019) and the randomForest package (Liaw and Wiener 2002) to predict daily inundation status (wet or dry) for individual wetlands. The random forest algorithm is an ensemble learning method that uses a collection of randomized decisions trees (James et al. 2013). Specifically, the random forest algorithm creates many decision trees from bootstrapped samples of training data. Each tree is grown from a random subset of predictor variables which helps to decorrelate the individual trees. For binary classification problems, the predicted classification results from the most frequent classification (i.e., majority votes) across all trees. Default values for random forest implementations often perform well even without hyperparameter tuning (Kuhn and Johnson 2013). However, there are several hyperparameters that can be tuned, often resulting in improved accuracy.
We used a grid search approach for the hyperparameters mtry (number of predictor variables available for splitting within a tree) and nodesize (minimum size of terminal nodes) and searched values ranging from 2 to 11 and 1–10, respectively, to find the best combination of values. Many combinations resulted in highly accurate predictions and very low out of bag error rates (OOB). Hyperparameter values were selected based on low OOB error rates that would also allow for greater randomization (i.e., smaller mtry) to help ensure decorrelated trees (James et al. 2021). For subsequent analyses of model performance and predictions the hyperparameters were set to mtry = 5 and nodesize = 2. We also set the number of trees to grow (ntree) to 300.
Another consideration in classification problems is the balance of observations within classes. In this case, the data were highly imbalanced (~ 5:1 – wet:dry). When this occurs, the models may simply target the majority class, because predicting those values alone will result in high accuracy and relatively low misclassification (Chen and Breiman 2004). We used variables within the randomForest implementation to achieve balance; namely, strata can be used to define the variable that sampling should be split over (in this case, wet and dry observations) and sampsize can be used to specify the same number of samples from each class. The minimum number of observations in a class (dry class) were used for setting up the balanced sampling. This resulted in downsampling the majority class, so that each class contributed an equal number of observations to the training data. We also used a cutoff value of 0.30 to assign a day as ‘dry,’ which indicates if 30% of all votes for a given site and day are “dry,” then that day should be classified as dry. This threshold was determined by stepping down the cutoff value from 0.50 (the default) to 0.25 by 0.05 and selecting the value that resulted in the greatest balanced accuracy of the validation set.
While random forests are robust to multicollinearity, the addition of correlated variables can make any attempt at drawing inference using variable importance metrics more difficult (Toloşi and Lengauer 2011). We used the usdm R-package (Naimi et al. 2014) to examine the variance inflation factors (VIF) of all paired predictor variables and used a VIF value of 5 as a cutoff for variable removal. This procedure resulted in the removal of 11 of the original 22 quantitative predictor variables (see Table 1). All variables removed due to high correlation were different lags of precipitation and potential evapotranspiration, and elevation standard deviation. This left the final models to consider the remaining topographic metrics, dominant vegetation class, ordinal day, and the water budget deficit over different antecedent periods for predicting inundation (Table 1).
Model Evaluation
It has been shown that error rates estimated from training data are often overly optimistic (James et al. 2021), which suggests relying on OOB error rates alone could lead to models with poor performance on unseen data. Therefore, we undertook a rigorous multi-faceted approach to model evaluation that tested performance on unseen wetlands and on unseen observations from wetlands in the training set. First, we split the data into training and validation groups using a stratified Monte Carlo cross validation approach (Kuhn and Johnson 2013), where all data from six randomly selected wetlands (2 each from permanent, frequently inundated, and infrequently inundated wetlands) were set aside as the “validation set.” The classification of “frequently” and “infrequently” inundated wetlands were based on the relative frequency of days that were observed to be inundated. The former class was greater than the median across all wetlands (79% of days) but non-permanent, and the latter class was wetlands whose inundation frequency was less than the median. This allowed an assessment of the effect of inundation frequency on model performance. The remaining data were randomly split into a 70/30 train/test sets (see Table S2 for evaluation of different data splitting strategies). Accuracy metrics on the test set demonstrate the predictability of the model on unseen observations from wetlands that had been used in training the model (similar to OOB error), whereas accuracy metrics on the validation set quantify the accuracy of the model predictions on completely unseen wetlands. This evaluation approach was conducted on 100 iterations to evaluate the stability of model predictions when different combinations of data were used to train, test, and validate the model predictions. To test for statistical differences in the observed and predicted median hydroperiods among the inundation classes we used the Brown-Mood median test in the coin R-package (Hothorn et al. 2006).
Results
Model Performance
From the 100-iteration cross validation routine, OOB error was 0.05–0.06, and the median balanced accuracy was 96% and 83% for the test and validation data, respectively (Fig. 3). Not surprisingly, performance was better on the test set because other data from these wetlands had been “seen” by the models. The relatively good and stable performance on the unseen wetlands indicated that the random forest classifier was a useful tool to explore the predictability of wetland inundation and hydroperiod.
Variable Importance and Interpretation
Variable importance was scaled to determine the proportional contribution of each predictor variable to overall classification accuracy (Fig. 4). Across most of the of model evaluations, topographic metrics were consistently in the top four most important variables regardless of which importance metric was used. Water budget deficit at a 60-day lag (def60) was also consistently among the most important predictor variables. The other variables also contributed to increasing classification accuracy but not as strongly, or as consistently, as the three topographic metrics and def60.
Considering the patterns of the top four variables, while holding all other variables constant, we observed highly non-linear relationships with inundation status (Fig. 5). A relatively linear relationship was present when def60 was below zero but rapidly leveled off above 100 mm. The relationships were more complex with the topographic predictors showing stepped, non-linear, and non-monotonic patterns. For example, the stepped pattern of basin averaged TPI (tpi_av_m) may indicate the presence of threshold values, where a decrease in the proportion of wet days occurred when the tpi_av_m is > -1 m and a further sharp decline as tpi_av_m approached − 0.5 m (Fig. 5).
Prediction of Wetland Inundation
The first check of model performance was to compare the number of wet and dry days between observations and predictions. We selected two infrequently inundated wetlands, one frequently inundated wetland, and one permanent wetland to highlight the dynamics reproduced by the model (Fig. 6). The top two plots of Fig. 6 represent infrequently inundated wetlands where predictions were relatively accurate. Wetland hawk demonstrated very accurate predictions of wet and dry periods capturing the general patterns and short-term dynamics (Fig. 6). The model also performed reasonably well on wetland rnd117; however, the short-term dynamics were not as well reproduced as those in hawk. At wetlands wpt79 (frequently inundated) and wpt150 (permanent) the general patterns were well reproduced by the models.
Considering model performance at the inundation class level, it is apparent that the median classification accuracy of infrequently inundated wetlands (0.92) was less similar to the observations than the frequently inundated wetlands or permanent wetlands (median = 0.98 and 0.99, respectively, Fig. 7). There was a greater occurrence of overprediction for the infrequent class compared to the frequent class, but all had a similar occurrence of under prediction (Fig. 7).
An examination of individual wetlands revealed additional insight regarding predictability and the stability of predictions. For example, wetland wpt57 (‘infrequent’ inundation category) showed an exceptional case where wetlands included in the training data were critical to accurate predictions (a value of 1 indicates perfect prediction, Fig. 8). At this wetland, five of the eight models from the cross-validation routine predicted the number of inundated days with 81–99% agreement; however, the other two models over predicted the number of days by 62% and 98%. Similar inaccuracies occurred at other wetlands (e.g., fn and rnd52); however, most of the extreme inaccuracies (those > 30%) were due to one or two outlying data points as most models were relatively precise. Wetlands in the other two inundation classes showed less variation in accuracy in response to changes in the training data, although there were exceptions (Fig. 8).
Estimating Hydroperiod
Because the ultimate goal of this study was predicting wetland hydroperiod – the duration of continuous inundation – we primarily focused our analysis on the non-permanent wetlands, and in these wetlands, we excluded periods of continuous inundation less than 30 days. This approach considered minimal periods that are meaningful for semi-aquatic biota, such as some rapidly developing anuran species (e.g., Gastrophryne carolinensis, Daszak et al. 2005) and reduced skewness of summary statistics associated with inclusion of a single to a few days of a particular inundation status (wet or dry).
Overall, prediction of hydroperiod was most accurate among the infrequent class, followed by the frequent class, with permanent wetlands having the greatest discrepancies (Fig. 9). For the infrequently inundated class, the test statistic for the Brown-Mood median test indicated a significant difference between the observed and predicted median hydroperiod (z = 3.325, p = < 0.0001, α = 0.05); however, the predicted and observed median hydroperiods only differed by 14 days. The frequently inundated wetlands also demonstrated a significant difference based on the median test (z = 7.2117, p = < 0.0001, α = 0.05), and the median predicted hydroperiod was 144 days less than the observed. While the permanent wetlands were not a primary focus, it is worth noting that they had the greatest discrepancy of a wetland class (Fig. 9).
The distribution of hydroperiods for individual wetlands provided additional insight regarding where the model performed best. Figure 10 displays the distribution of the estimated hydroperiods for individual wetlands across all the cross-validation iterations compared to the observed distribution of hydroperiods. Figure 10 demonstrates that the predictability of hydroperiod was inconsistent across wetlands even within a given inundation class. For example, the infrequently inundated category wetlands fn and wbf demonstrated good agreement in the median hydroperiods, only differing by 6 and 14 days, respectively. In contrast, the models generally overpredicted hydroperiods in wetland rnd75, with the predicted median hydroperiod 68 days longer than observed. Wetlands from the frequently inundated category showed much greater variability and discrepancy between observed and predicted hydroperiods (Fig. 10). Wetlands jr36 and borrow405 were predicted the most accurately of those in Fig. 10 (right panel), but they still differed considerably from the observed median hydroperiod by 61 and 101 days, respectively. The remaining wetlands in the frequently inundated category had much greater discrepancy in predicted and observed hydroperiods. In many cases the models tended to produce rather narrow ranges of hydroperiods that underestimated the high-end of the distribution of many wetlands (Fig. 10). The models did not show a particular bias in either of the inundation classes; rather, results across individual wetlands showed both under and over prediction.
Discussion
Drivers of Inundation and Hydroperiod
Controls on wetland hydroperiod will vary depending on topographic position within the landscape and hydrogeologic setting. However, the overarching drivers are related to the water budget of a site and the ability of a basin to hold water (i.e., its volume, shape, and geological material). As Fig. 4 demonstrates, both water budget and basin morphology were important for accurate prediction of wetland inundation. While some studies highlight that mean decrease in accuracy is a more robust (less biased) variable importance metric (Strobl et al. 2007; Genuer et al. 2010), Boulesteix et al. (2012) indicates that mean decrease in gini impurity is more appropriate for classification with imbalanced classes. However, in this study both metrics generally agreed and ranked the same four variables as the most important, albeit in a slightly different order.
Many studies spanning a wide range of wetland types and climates have also observed basin morphology (topography or depth) to be a key variable related to hydroperiod (Brooks and Hayashi 2002; Pyke 2004; Garmendia and Pedrola-Monfort 2010; Greenberg et al. 2015; Chandler et al. 2016). Thus, this study’s modeling approach could be useful in other areas where topography exerts a strong control on water permanence, such as in northeastern United States vernal pools or in the prairie pothole region of North America. Many studies attempting to predict wetland inundation dynamics have found antecedent precipitation to be important for accurate prediction (e.g. Bartuszevige et al. 2012; Chandler et al. 2016; Solvik et al. 2021; Londe et al. 2022). In this study, however, antecedent water budget deficits (precipitation minus potential evapotranspiration) were more important predictors of inundation than precipitation. The transferability of the water budget deficit at a 60-day lag to other regions is less straightforward and the importance of this variable likely varies depending on soil texture, water table depth, and the hydroclimatology of a region. We believe this intermediate antecedent period (60 days) may integrate aspects of storage from the vadose and saturated zones in this study region making it consistently more important than shorter- or longer-term lags that may be more reflective of one or the other storage components. In regions with greater topographic relief, or with clayey soil horizons that inhibit rapid infiltration, it is probable that shorter antecedent periods may be of more importance than were observed in this study because lateral flows following rainfall could be primary drivers of inundation (e.g., Winter 1988; Winter 1999; Bartuszevige et al. 2012).
Model Performance
Compared to other studies that have predicted inundation and hydroperiod dynamics, our median balanced accuracy across models of 83% was higher than that reported by several other studies (80% [Londe et al. 2022], 76% [Greenberg et al. 2015], and 73% [Chandler et al. 2016]). However, it is difficult to directly compare model accuracy between different studies because each study’s models were intended for different applications with different temporal resolutions. For example, in this study we were making predictions at a daily time step; thus, misclassifying a single day effectively divides one hydroperiod into two, resulting in “poor” model performance. In contrast, many other studies have used infrequent observations of wetlands, either flooded extent or some metric of wetland water depth, to infer hydroperiods and often have focused on specific periods relevant to target taxa or species – most frequently amphibians (e.g., Babbitt 2005; Chandler et al. 2016; Cartwright et al. 2021; Solvik et al. 2021). While infrequent observation is certainly reasonable given the cost and difficulty of continuous (or near continuous) water presence observation, it does introduce the potential for missing a drying event or even very short-term filling and subsequent drying. As Chandler et al. (2016) acknowledged, only a single drying event (day) is necessary to induce mortality of larval salamanders. Furthermore, focusing on a single short period (i.e., breeding season) may obscure other important aspects of hydroperiod that relate to development of predators, prey, and habitats associated with the wetted duration prior to the focal period (Pechmann et al. 1989). Much of the literature rightly focuses on the wetted hydroperiod; however, some amphibian species (e.g., the threatened Ambystoma cingulatum) only lay their eggs in dry pond basins (Anderson and Williamson 1976). Therefore, knowing the drying regime may be just as important for some wetland species. This is especially true in the face of climate change and high uncertainty in future precipitation regimes of the southeastern United States (Carter et al. 2018; LaFontaine et al. 2019).
To capture the full suite of wetting and drying periods, we set out to predict hydroperiod continuously at a daily timestep – a process that could be useful for multiple taxa with various phenological and hydrologic requirements. Our results indicated that the models performed quite well, although there were wetlands that were less well predicted (Figs. 8 and 10). The finding of statistically significant differences between the predicted and observed hydroperiods (Fig. 9) in wetlands of all inundation classes doesn’t necessarily translate to biological significance. Whether such deviations are biologically meaningful will depend on individual species and their hydrologic requirements.
The large discrepancies we found between observed and predicted hydroperiods in the permanent wetlands was not overly surprising. As an example, if a permanent wetland had only a single day that was misclassified by the model in the middle of the record, then the hydroperiod estimate would be half of the observed inundated period. If this were to occur twice, the discrepancy would increase accordingly. Thus, viewing the results at this high level provides insights into where the models performed best, but did not tell the full story. This is in stark contrast to the analysis of inundation frequency, where the permanent inundation class was 99% accurate, highlighting the importance in choosing the most appropriate metric(s) and examining details for interpretation of model performance and any management implications. In cases where inundation frequency was accurate and hydroperiod was not, it could be assumed that a small number of misclassified days led to the discrepancy, and model output still contains valuable information. However, in these cases more human intervention is needed to interpret the results and define what is meaningful or at an acceptable level of accuracy. Another factor we did not explicitly consider in this study was the timing of filling and drying events. This is of critical importance because for a hydroperiod to be biologically meaningful, it must align with the phenology of a specific species. Based on the subset of wetlands presented in Fig. 4, it appears the models matched the timing of filling and drying accurately. Follow up analyses to quantify model performance related to the timing of filling and drying would best be conducted utilizing species-specific examples with biological survey data. Doing so would then allow for predicted inundation characteristics to be extended to evaluate and identify habitats of concern for the long-term conservation of populations.
Comparisons to Other Modeling Techniques
Unlike physically based process models, ML models are geared towards prediction rather than process understanding, although some insight into controlling variables can be gleaned when model parsimony is rigorously constrained (Fig. 4). If intensive site level data and the expertise to implement a physically based process model are available, then predictions and process-level insight could potentially be provided. However, if the main goal is prediction, ML approaches offer a robust alternative and may require less intensive field data for suitable predictions.
Machine learning models can be trained on extensive datasets (where they exists) and applied in other situations or locations where the phenomenon of interest operates on similar processes, such as where topography is thought to exert a strong control on wetland hydroperiod. Thus, practitioners could apply this modeling framework by deriving the input variables highlighted in Table 1 to explore the accuracy in other study areas. Additionally, as more field data become available it could be combined with the data used here to retrain models so patterns from other regions can also be learned and incorporated, making predictions more generalizable. If other predictor variables are identified that are critical to a given region (e.g., soil or bedrock type), the models could be updated to include the additional information. This modeling approach and associated predictors performed well in our study area; however, that does not mean it will work everywhere. Therefore, when applying such a framework it is critical to have some way of validating that the predictions are reasonable, whether through limited monitoring, remote sensing, or by correlations with antecedent weather conditions.
A final point worth reiterating is that the present approach is simply predicting whether water was present or not based on the threshold water-level. We recognize this is a rather crude representation of wetland hydrology and it neglects the spatial dynamics that are often critical for providing diverse habitat types, such as open water and marsh within the same basin (Cowardin et al. 1979; Pechmann et al. 1989). However, linking continuous water level measurements to inundated area requires considerable field work to develop these stage-area relationships. Furthermore, we believe there are many wetland water level datasets waiting to be uncovered that could be integrated into this modeling framework to extend predictions to other areas and refine the present work. Therefore, we chose to focus on a presence/absence type prediction rather than some more complex metric such as areas or volumes. This somewhat naïve view of “wetness” could be too simplistic in wetlands with high degrees of microtopographic relief that lead to isolated pools disconnected from a central basin. Even in those cases it may be that a suitable threshold water level could be targeted to reflect the most important habitat characteristics still rendering a similar approach useful.
Critical Need for Monitoring data
This modeling effort would not have been possible without the extensive dataset which represents a considerable effort of many people and investment of resources. Therefore, we would like to highlight the importance of field data and long-term records. If similar monitoring networks to the one used here, even with far fewer wetlands, could be established (or brought to light where they exist) it could allow similar efforts to be conducted over greater spatial scales to build models that are appropriate for broader areas and wetland types. This could go a long way to further the wetland communities’ ability to predict inundation dynamics in depressional wetlands which could increase our understanding of habitat diversity across broader landscapes. While this study relied on surface water level data, most any type of observational data (e.g., iButtons, [Anderson et al. 2015], or citizen observations [North et al. 2023]) can be helpful in furthering our understanding of wetland hydrology as long as the methods used and data quality are properly documented.
Conclusions
In this study we demonstrated the predictability of daily wetland inundation dynamics and hydroperiod using random forests and predictor variables that were derived from a GIS environment using readily available datasets for the conterminous United States (Table 1). The random forests were trained and evaluated using an extensive dataset containing water levels from 59 wetlands to predict whether a wetland was inundated or not on a given day. The models had low error rates (OOB = 0.05–0.06), good balanced accuracy (median = 83%), and were able to predict median hydroperiod most accurately in infrequently inundated wetlands and least accurate in permanent wetlands. However, a different pattern was observed when considering the total number of inundated days – with permanent wetlands the most accurate (99%) and infrequently inundated wetlands, the least (93%). This suggested the choice of metric can provide different insights into model performance, and considering both metrics together can give a more complete picture of model performance and where the models may be most useful. Wetland inundation dynamics and hydroperiod are key controls on most wetland functions. Improving our ability to predict these dynamics will be beneficial to researchers and managers alike. Where validation data exist, the approach described here has the potential to expand our understanding of inundation dynamics of small depressional wetlands to be better prepared for the evolving conservation needs of these critical habitats in the future.
Data Availability
All data used in the study are publicly available. The wetland water-level data used in this study are stored in the USGS ScienceBase-Catalog and available at: https://doi.org/10.5066/F7C827CC. Meteorological data were from gridMET available at: https://www.climatologylab.org/gridmet.html. The digital elevation model used to derive topographic data was from the 2007 Florida Division of Emergency Management lidar collection for Wakulla County (FDEM 2008). Available at: https://coast.noaa.gov/dataviewer/#/lidar/search/where:ID=552/details/552.
References
Abatzoglou JT (2013) Development of gridded surface meteorological data for ecological applications and modelling. Int J Climatol 33:121–131. https://doi.org/10.1002/joc.3413
Alonso A, Muñoz-Carpena R, Kaplan D (2020) Coupling high-resolution field monitoring and MODIS for reconstructing wetland historical hydroperiod at a high temporal frequency. Remote Sens Environ 247:111807. https://doi.org/10.1016/j.rse.2020.111807
Anderson JD, Williamson GK (1976) Terrestrial mode of reproduction in Ambystoma cingulatum. Herpetologica 214–221
Anderson TL, Heemeyer JL, Peterman WE et al (2015) Automated analysis of temperature variance to determine inundation state of wetlands. Wetlands Ecol Manage 23:1039–1047. https://doi.org/10.1007/s11273-015-9439-x
Babbitt KJ (2005) The relative importance of wetland size and hydroperiod for amphibians in southern New Hampshire, USA. Wetlands Ecol Manage 13:269–279. https://doi.org/10.1007/s11273-004-7521-x
Babbitt KJ, Baber MJ, Tarr TL (2003) Patterns of larval amphibian distribution along a wetland hydroperiod gradient. Can J Zool 81:1539–1552. https://doi.org/10.1139/z03-131
Bartuszevige AM, Pavlacky DC, Burris L, Herbener K (2012) Inundation of Playa Wetlands in the Western Great Plains relative to Landcover Context. Wetlands 32:1103–1113. https://doi.org/10.1007/s13157-012-0340-6
Best MJ, Abramowitz G, Johnson HR et al (2015) The plumbing of Land Surface Models: Benchmarking Model performance. J Hydrometeorol 16:1425–1442. https://doi.org/10.1175/JHM-D-14-0158.1
Boulesteix A-L, Janitza S, Kruppa J, König IR (2012) Overview of random forest methodology and practical guidance with emphasis on computational biology and bioinformatics. WIREs Data Min Knowl Discov 2:493–507. https://doi.org/10.1002/widm.1072
Breiman L (2001) Random forests. Mach Learn 45:5–32. https://doi.org/10.1023/A:1010933404324
Brooks RT, Hayashi M (2002) Depth-area-volume and hydroperiod relationships of ephemeral (vernal) forest pools in southern New England. Wetlands 22:247–255. https://doi.org/10.1672/0277-5212(2002)022[0247:DAVAHR]2.0.CO;2
Caldwell PeterV, Vepraskas MichaelJ, Skaggs RW, Gregory JamesD (2007) Simulating the water budgets of natural Carolina bay wetlands. Wetlands 27:1112–1123. doi: https://doi.org/10.1672/0277-5212(2007)27[1112:STWBON]2.0.CO;2
Carter L, Terando A, Dow K et al (2018) Chap. 19: Southeast. Impacts, Risks, and Adaptation in the United States: The Fourth National Climate Assessment, Volume II
Cartwright JM, Wolfe WJ (2021) Increasing Hydroperiod in a karst-depression Wetland based on 165 years of simulated daily water levels. Wetlands 41:75. https://doi.org/10.1007/s13157-021-01474-x
Cartwright J, Morelli TL, Grant EHC (2021) Identifying climate-resistant vernal pools: hydrologic refugia for amphibian reproduction under droughts and climate change. Ecohydrology n/a:e2354. https://doi.org/10.1002/eco.2354
Chandler HC, Rypel AL, Jiao Y et al (2016) Hindcasting historical breeding conditions for an endangered salamander in Ephemeral Wetlands of the Southeastern USA: implications of Climate Change. PLoS ONE 11:e0150169. https://doi.org/10.1371/journal.pone.0150169
Chen C, Breiman L (2004) Using Random Forest to learn Imbalanced Data. University of California, Berkeley
Choi C, Kim J, Han H et al (2020) Development of Water Level Prediction Models using machine learning in wetlands: a case study of Upo Wetland in South Korea. Water. https://doi.org/10.3390/w12010093
Cohen MJ, Creed IF, Alexander L et al (2016) Do geographically isolated wetlands influence landscape functions? Proc Natl Acad Sci 113:1978–1986. https://doi.org/10.1073/pnas.1512650113
R Core Team (2019) R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL https://www.R-project.org/
Cowardin LM, Carter V, Golet FC, LaRoe ET (1979) Classification of wetlands and deepwater habitats of the United States. Washington, DC
Craft C, Vymazal J, Kröpfelová L (2018) Carbon sequestration and nutrient accumulation in floodplain and depressional wetlands. Wetlands and Carbon Revisited 114:137–145. https://doi.org/10.1016/j.ecoleng.2017.06.034
Daszak P, Scott DE, Kilpatrick AM et al (2005) Amphibian population declines at savannah river site are linked to climate, not chytridiomycosis. Ecology 86:3232–3237. https://doi.org/10.1890/05-0598
Davis CL, Miller DAW, Campbell Grant EH et al (2019) Linking variability in climate to wetland habitat suitability: is it possible to forecast regional responses from simple climate measures? Wetlands Ecol Manage 27:39–53. https://doi.org/10.1007/s11273-018-9639-2
Dodd CK Jr (1992) Biological diversity of a temporary pond herpetofauna in north Florida sandhills. Biodivers Conserv 1:125–142. https://doi.org/10.1007/BF00695911
Dodd CK (1993) Cost of living in an unpredictable environment: the Ecology of Striped Newts Notophthalmus perstriatus during a prolonged Drought. Copeia 1993:605–614. https://doi.org/10.2307/1447221
FDEM (2008) 2007 Florida Division of Emergency Management (FDEM) Lidar Project: Wakulla County. Available at: https://noaa-nos-coastal-lidar-pds.s3.amazonaws.com/laz/geoid12a/552/index.html
Galeati G (1990) A comparison of parametric and non-parametric methods for runoff forecasting. Hydrol Sci J 35:79–94. https://doi.org/10.1080/02626669009492406
Garmendia A, Pedrola-Monfort J (2010) Simulation model comparing the hydroperiod of temporary ponds with different shapes. Limnetica 29:145–152
Genuer R, Poggi J-M, Tuleau-Malot C (2010) Variable selection using random forests. Pattern Recognit Lett 31:2225–2236. https://doi.org/10.1016/j.patrec.2010.03.014
Greenberg CH, Goodrick S, Austin JD, Parresol BR (2015) Hydroregime Prediction Models for Ephemeral Groundwater-Driven Sinkhole Wetlands: a Planning Tool for Climate Change and Amphibian Conservation. Wetlands 35:899–911. https://doi.org/10.1007/s13157-015-0680-0
Gunzburger MS, Hughes WB, Barichivich WJ, Staiger JS (2010) Hurricane storm surge and amphibian communities in coastal wetlands of northwestern Florida. Wetlands Ecol Manage 18:651–663. https://doi.org/10.1007/s11273-010-9185-z
Hopkinson C, Fuoco B, Grant T et al (2020) Wetland Hydroperiod Change Along the Upper Columbia River Floodplain, Canada, 1984 to 2019. Remote Sensing. doi: https://doi.org/10.3390/rs12244084
Hothorn T, Hornik K, van de Wiel MA, Zeileis A (2006) A Lego system for conditional inference. Am Stat 60(3):257–263. https://doi.org/10.1198/000313006X118430
James G, Witten D, Hastie T, Tibshirani R (2013) An introduction to statistical learning. Springer
Jenness J, Brost B, Beier P (2011) Land facet corridor designer: extension for ArcGIS. Jenness enterprises. Available from: http://www.jennessent.com/arcgis/land_facets.htm. Accessed 12 Mar 2023
Johnson M (2021) climateR: climateR. R package version 0.1.0. https://github.com/mikejohnson51/climateR
Jones JW (2015) Efficient wetland surface water detection and monitoring via Landsat: comparison with in situ data from the everglades depth Estimation Network. Remote Sens 9:12503–12538. https://doi.org/10.3390/rs70912503
Jones JW (2019) Improved automated detection of subpixel-scale inundation – revised dynamic Surface Water Extent (DSWE) partial surface water tests. Remote Sens 11:1–26. https://doi.org/10.3390/rs11040374
Kissel AM, Halabisky M, Scherer RD et al (2020) Expanding wetland hydroperiod data via satellite imagery for ecological applications. Front Ecol Environ 18:432–438. https://doi.org/10.1002/fee.2233
Krasnostein AL, Oldham CE (2004) Predicting wetland water storage. Water Resour Res. https://doi.org/10.1029/2003WR002899
Kuhn M, Johnson K (2018) Applied predictive modeling. Springer
Kurki-Fox JJ, Burchell MR, Kamrath BJ (2019) The potential long-term impacts of Climate Change on the hydrologic regimes of North Carolina’s Coastal Plain Non-Riverine Wetlands. Trans ASABE 62:1591–1606. https://doi.org/10.13031/trans.13437
LaFontaine JH, Hart RM, Hay LE et al (2019) Simulation of water availability in the Southeastern United States for historical and potential future climate and land-cover conditions. https://doi.org/10.3133/sir20195039
LANDFIRE (2016) Existing Vegetation Type Layer, LANDFIRE 2.0.0, U.S. Department of the Interior, Geological Survey, and U.S. Department of Agriculture. Accessed 10 June 2021 at http://www.landfire/viewer
Liaw A, Wiener M (2002) Classification and regression by randomForest. R News 2:18–22
Londe DW, Dvorett D, Davis CA et al (2022) Inundation of depressional wetlands declines under a changing climate. Clim Change 172:27. https://doi.org/10.1007/s10584-022-03386-z
Marton JM, Creed IF, Lewis DB et al (2015) Geographically isolated wetlands are important Biogeochemical reactors on the Landscape. Bioscience 65:408–418. https://doi.org/10.1093/biosci/biv009
McLaughlin DL, Cohen MJ (2011) Thermal artifacts in measurements of fine-scale water level variation. Water Resour Res. https://doi.org/10.1029/2010WR010288
McLaughlin DL, Cohen MJ (2012) Ecosystem specific yield for estimating evapotranspiration and groundwater exchange from diel surface water variation. Hydrol Process 28:1495–1506. https://doi.org/10.1002/hyp.9672
McLaughlin DL, Kaplan DA, Cohen MJ (2014) A significant nexus: geographically isolated wetlands influence landscape hydrology. https://doi.org/10.1002/2013WR015002. Water Resources Research n/a-n/a
Mitsch W, Gosselink J (2015) Wetlands, 5th edition
Murdock NA (1995) Rare and endangered plants and animals of Southern Appalachian Wetlands. In: Trettin CC, Aust WM, Wisniewski J (eds) Wetlands of the Interior Southeastern United States. Springer Netherlands, Dordrecht, pp 189–209
Murray-Hudson M, Wolski P, Cassidy L et al (2015) Remote sensing-derived hydroperiod as a predictor of floodplain vegetation composition. Wetlands Ecol Manage 23:603–616. https://doi.org/10.1007/s11273-014-9340-z
Naimi B, Hamm N, a s, Groen TA et al (2014) Where is positional uncertainty a problem for species distribution modelling. Ecography 37:191–203. https://doi.org/10.1111/j.1600-0587.2013.00205.x
NCDWR, NC Division of Water Resources (2018). 2018–2023. North Carolina Wetlands Information. https://www.ncwetlands.org. Published by the North Carolina Division of Water Resources, Water Sciences Section. Accessed 03 April 2023
Nearing GS, Mocko DM, Peters-Lidard CD et al (2016) Benchmarking NLDAS-2 soil moisture and evapotranspiration to separate uncertainty contributions. J Hydrometeorol 17:745–759. https://doi.org/10.1175/JHM-D-15-0063.1
Nearing GS, Kratzert F, Sampson AK et al (2021) What role does Hydrological Science Play in the age of machine learning? Water Resour Res 57. https://doi.org/10.1029/2020WR028091. e2020WR028091
North T, Moore P, Birch W et al (2023) iWetland: A Community Science platform for Monitoring Wetland Water levels. Citiz Science: Theory Pract 8:7. https://doi.org/10.5334/cstp.448
Pechmann J, Scott D, Gibbons J, Semlitsch R (1989) Influence of wetland hydroperiod on diversity and abundance of metamorphosing juvenile amphibians. Wetlands Ecol Manage 1:3–11. https://doi.org/10.1007/BF00177885
Pyke CR (2004) Simulating vernal pool hydrologic regimes for two locations in California, USA. Ecol Model 173:109–127. https://doi.org/10.1016/j.ecolmodel.2003.08.014
Qi J, Zhang X, Lee S et al (2019) A coupled surface water storage and subsurface water dynamics model in SWAT for characterizing hydroperiod of geographically isolated wetlands. Adv Water Resour 131:103380. https://doi.org/10.1016/j.advwatres.2019.103380
Rains MC, Leibowitz SG, Cohen MJ et al (2016) Geographically isolated wetlands are part of the hydrological landscape. Hydrol Process 30:153–160. https://doi.org/10.1002/hyp.10610
Reddy KR, DeLaune RD (2008) Biogeochemistry of wetlands: science and applications. CRC press
Riley JW (2016) Water level data from select depressional wetlands at Saint Marks National Wildlife Refuge: July 2010 - May 2019 (version. 2.0, April 2022), U.S. Geological Survey data release, https://doi.org/10.5066/F7C827CC
Riley JW, Calhoun DL, Barichivich WJ, Walls SC (2017) Identifying small depressional wetlands and using a topographic position index to infer hydroperiod regimes for pond-breeding amphibians. Wetlands 37:325–338. https://doi.org/10.1007/s13157-016-0872-2
Shaeri Karimi S, Saintilan N, Wen L, Valavi R (2019) Application of machine learning to Model Wetland inundation patterns across a large Semiarid Floodplain. Water Resour Res 55:8765–8778. https://doi.org/10.1029/2019WR024884
Shen C, Chen X, Laloy E (2021) Editorial: broadening the Use of Machine Learning in Hydrology. Front Water. https://doi.org/10.3389/frwa.2021.681023
Skaggs RW, Chescheir GM, Phillips BD (2005) Method to determine lateral effects of a drainage ditch on wetland hydrology. Trans ASAE 48(2):577–584. https://doi.org/10.13031/2013.18332
Smith LL, Subalusky AL, Atkinson CL et al (2019) Biological connectivity of seasonally ponded wetlands across spatial and temporal scales. JAWRA J Am Water Resour Association 55:334–353. https://doi.org/10.1111/1752-1688.12682
Snodgrass JW, Komoroski MJ, Bryan JR, AL, Burger J (2000) Relationships among isolated wetland size, Hydroperiod, and Amphibian Species Richness: implications for Wetland Regulations. Conserv Biol 14:414–419. https://doi.org/10.1046/j.1523-1739.2000.99161.x
Solomatine DP, Ostfeld A (2008) Data-driven modelling: some past experiences and new approaches. J Hydroinformatics 10:3–22. https://doi.org/10.2166/hydro.2008.015
Solvik K, Bartuszevige AM, Bogaerts M, Joseph MB (2021) Predicting Playa Inundation using a long short-term memory neural network. Water Resour Res 57. https://doi.org/10.1029/2020WR029009. e2020WR029009
Statements & Declarations
Strobl C, Boulesteix A-L, Zeileis A, Hothorn T (2007) Bias in random forest variable importance measures: illustrations, sources and a solution. BMC Bioinformatics 8:25. https://doi.org/10.1186/1471-2105-8-25
Sun G, Riekerk H, Comerford NB (1998) Modeling the forest hydrology of wetland-upland ecosystems in florida1. JAWRA J Am Water Resour Association 34:827–841. https://doi.org/10.1111/j.1752-1688.1998.tb01519.x
Sun G, Riekerk H, Comerford N (2007) Modeling the hydrologic impacts of Forest Harvesting on Florida Flatwoods. JAWRA J Am Water Resour Association 34:843–854. https://doi.org/10.1111/j.1752-1688.1998.tb01520.x
Toloşi L, Lengauer T (2011) Classification with correlated features: unreliability of feature ranking and solutions. Bioinformatics 27:1986–1994. https://doi.org/10.1093/bioinformatics/btr300
Tyralis H, Papacharalampous G, Langousis A (2019) A brief review of Random forests for Water scientists and practitioners and their recent history in Water Resources. Water. https://doi.org/10.3390/w11050910
Weiss A (2001) Topographic Position and Landforms Analysis. Poster presentation, ESRI User Conference, San Diego, CA.Conference, San Diego, CA
Williams JD, Dodd CK Jr (1978) Importance of wetlands to endangered and threatened species. Wetland functions and values: the state of our understanding 565–575
Winter TC (1988) A conceptual framework for assessing cumulative impacts on the hydrology of nontidal wetlands. Environ Manage 12:605–620. https://doi.org/10.1007/BF01867539
Winter TC (1999) Relation of streams, lakes, and wetlands to groundwater flow systems. Hydrogeol J 7:28–45. https://doi.org/10.1007/s100400050178
Wu Q, Lane CR, Li X et al (2019) Integrating LiDAR data and multi-temporal aerial imagery to map wetland inundation dynamics using Google Earth Engine. Remote Sens Environ 228:1–13. https://doi.org/10.1016/j.rse.2019.04.015
Zounemat-Kermani M, Batelaan O, Fadaee M, Hinkelmann R (2021) Ensemble machine learning paradigms in hydrology: a review. J Hydrol 598:126266. https://doi.org/10.1016/j.jhydrol.2021.126266
Acknowledgements
We acknowledge the U.S. Geological Survey (USGS) South Atlantic Water Science Center for funding the initial pilot study this analysis was built upon. Additional funding was provided by the USGS Amphibian Research Monitoring Initiative (ARMI). We also thank Jennifer Cartwright (USGS) and anonymous reviewers for valuable feedback that greatly improved this manuscript. This is contribution Number 876 of the U.S. Geological Survey Amphibian Research and Monitoring Initiative (ARMI). Any use of trade, firm, or product names is for descriptive purposes only and does not imply endorsement by the U.S. Government.
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Riley, J.W., Stillwell, C.C. Predicting Inundation Dynamics and Hydroperiods of Small, Isolated Wetlands Using a Machine Learning Approach. Wetlands 43, 63 (2023). https://doi.org/10.1007/s13157-023-01706-2
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DOI: https://doi.org/10.1007/s13157-023-01706-2