- Research
- Open Access
The effects of nutrients on stream invertebrates: a regional estimation by generalized propensity score
- Zutao Ouyang^{1}Email authorView ORCID ID profile,
- Song S. Qian^{2},
- Richard Becker^{2} and
- Jiquan Chen^{1}
- Received: 23 January 2018
- Accepted: 11 May 2018
- Published: 4 June 2018
Abstract
Introduction
The effects of nutrients on stream conditions within individual streams or small areas have been studied extensively, but the same effects over a large region have rarely been examined due to the difficulty of applying large-scale manipulative experiments. In this study, we estimated the causal effects of nutrients within the Western United States on invertebrate richness, an important biological indicator of stream conditions, by using observational data.
Methods
We used the generalized propensity score method to avoid the common problem of statistical inference using observational data, i.e., correlation established based on observational data does not imply a causal relationship because the effects of confounding factors are not properly separated.
Results
Our analysis showed a subsidy-stress relationship between nutrients and invertebrate taxon richness in the whole Western United States and in its sub-ecoregions. The magnitude of the relationship varies among these sub-ecoregions, suggesting a varying nitrogen effect on macroinvertebrates due, in large part, to the varying natural and anthropogenic conditions from ecoregion to ecoregion. Furthermore, our analysis confirmed that causal estimation results using regression can be sensitive to the imbalance of confounding factors.
Conclusions
Stratifying data into ecoregions with relatively homogeneous environmental conditions or adjusting data by generalized propensity score can improve the balance of confounding factors, thereby allowing more reliable causal inference of nutrient effects. Invertebrates respond to the same nutrient levels differently across different site conditions.
Keywords
- Nutrient criteria
- Water quality
- Environmental management
- Ecoregion
Introduction
Nutrients are essential for maintaining an ecosystem’s structure and function. Knowledge of the effects of excessive nutrients on ecosystems is important for environmental management. In streams, increased nutrient concentrations have altered biological structures and functions such as species richness, composition, abundance, and decomposition rate (Dodson et al. 2000; Freeman et al. 2009; Smith et al. 1999; Gulis and Suberkropp 2004; Rosemond et al. 1993). Excessive nutrients can also reduce water quality causing problems for drinking water and can deplete dissolved oxygen, leading to fish kills (USEPA 1996). For example, 40% of rivers in the USA have been impaired primarily as a result of excessive nutrients (USEPA 1996).
Invertebrates occupy an important ecological niche in streams, and their aggregated measures such as total taxon richness are widely used for stream condition assessments (Fore et al. 1996; Moss et al. 1987). However, while a few key invertebrate taxon grazers have been examined in many field and laboratory studies, relatively little work has been done to examine the effects of nutrients on aggregate measures of invertebrate assemblages (e.g., richness) (Yuan 2010; Cross et al. 2006; Quinn et al. 1997). As a result, our current understanding of the causal effects between increased nutrients and invertebrate richness (IR) is still limited.
How responsively does the IR change with nutrients, and does the causal relationship vary regionally? The causal relationship details are necessary to inform management actions and provide proper measures. A causal relationship is ideally quantified using manipulative experiments where treatments are randomly applied to replicated samples. This approach eliminates the effects of confounding factors by adequately resolving the counterfactual problem (Maldonado and Greenland 2002) in a causal analysis. Such manipulative studies (e.g., Cross et al. 2006; Gafner and Robinson 2007; Hart and Robinson 1990; Slavik et al. 2004) have increased our understanding of the effects of nutrients on streams but were usually conducted in a very small area or single whole stream/channel representing limited conditions. As a result, it is difficult to draw general conclusions from those studies for a region (e.g., the regional average effect) for setting regional nutrient criteria. Applying randomized experiments is difficult in the case of many streams across a large landscape. An alternative approach to study regional average effect is to use observational data that have been collected from many streams spanning different conditions/locations, which might produce complemental knowledge to that what we have gained from manipulative studies.
Observational data, by definition, are collected without a random sampling mechanism with respect to the effect of the variable of interest. When observational data are used without properly addressing potential problems induced by the non-random nature of the data collection process (e.g., imbalance of factors other than the variable of interest, i.e., confounding factors), results can be biased (Qian and Harmel 2016). However, rare studies in the ecological literature have addressed this problem of confounding factors, which can lead to divergent results of the same problem. For example, Clenaghan et al. (1998) reported a positive association between nutrients and benthic macroinvertebrates in one catchment in Ireland; Heino et al. (2003) reported the same positive association in a river in Finland; Bergfur et al. (2007) found a negative correlation in streams of central Sweden; Wang et al. (2007) demonstrated a negative association in some wadeable streams in Wisconsin; and Harding et al. (1999) and Niyogi et al. (2007) showed no clear link between macroinvertebrates and nutrient concentrations in one river and in a suite of 21 streams of southern New Zealand, respectively. These divergent results are expected, as these studies focused on local streams and each stream may have different confounding factors (e.g., watershed land use patterns, habitat quality, and flow conditions). Because nutrient criteria are usually developed for a large geographic region and not for individual streams or at a local level, understanding the regional (average) effects of nutrient enrichment is necessary. In this study, we aim to evaluate the regional average effects of nutrients on stream invertebrate taxon richness in the Western United States and its individual ecoregions from observational data.
An effect, or more specifically a causal effect, of a nutrient on invertebrate richness cannot be equated to the correlation between the two variables when the data used are observational data. In observational data, a treatment (i.e., nitrogen concentrations) is “assigned” to each site through some unknown and likely non-random processes. The resulting data are not balanced with respect to confounding factors. In other words, observed values of a confounding factor cannot be the same for streams with different observed treatment levels (nitrogen concentration). This imbalance often leads to a biased estimate of the causal relationship. One statistical approach to this problem is the use of propensity score matching (Rosenbaum and Rubin 1983; Rubin 2006). The propensity score matching approach was designed for binary treatment variables. It has been used for assessing the effectiveness of agricultural conservation practices on nutrient loss (Qian and Harmel 2016). In our study, the treatment variable, nitrogen concentration, is a continuous variable. We use the generalized propensity score method (Hirano and Imbens 2004; Imai and van Dyk 2004), which estimates the causal relationship by averaging out the effects of known confounding factors. The generalized propensity score for continuous treatments is an extension of the well-established and widely used propensity score methodology for binary treatments (Rosenbaum and Rubin 1983) and multivalued treatments (Rubin 2006).
Here, we used the generalized propensity score method of Hirano and Imbens (2004). This method does not presume any specific linear or nonlinear relationship and allows for flexibility. Our specific questions were “How does the invertebrate taxon richness change with increased eutrophication in the Western United States, and does this causal relationship vary by ecoregion?” Answers to these questions can provide baseline scientific information for nutrient criteria development.
Methods
Data
Covariates of total nitrogen (TN) included in the study and their correlation with log (TN) within all streams
Variable | Description | Units | r |
---|---|---|---|
ELEV | Elevation | m | − 0.18 |
Longitude | Longitude | Degree | 0.57 |
Log(PRECIP) | Annual precipitation in log scale | mm | − 0.58 |
Log(AREA) | Catchment area in log scale | km^{2} | 0.47 |
Log(CL) | Cl^{−} concentration in log scale | μg/L | 0.62 |
Log(HCO3) | HCO_{3}^{−} concentration in log scale | μg/L | 0.55 |
Log(SO4) | SO_{4}^{−2} concentration in log scale | μg/L | 0.61 |
SED | Sand and fine substrate in the stream (< 2 mm in diameter) | μg/L | 0.63 |
STRMTEMP | Stream temperature | Degree | 0.49 |
Percent.AGT | Percentage of catchment in agricultural land use | μg/L | 0.57 |
Percent.URB | Percentage of catchment in urban land | Percentage | 0.30 |
Percent.Canopy | Percentage of open canopy | Percentage | 0.47 |
Riparian.Disturb | Riparian agricultural disturbance index | Index | 0.49 |
We considered 13 important covariates (variables that co-varied with nutrient concentration) as major confounding factors of the TN-IR dose-response relationship (Table 1). Covariates were identified by examining bivariate scatter plots and by investigating the correlation between TN and each candidate variable. We used variables with statistically significant correlation with TN (p < 0.05). Methods of field collection and variable extraction of the 13 covariates can be found in Yuan (2010) and Stoddard et al. (2006). TN, precipitation, and other chemistry measurements (e.g., chloride ion) were highly skewed and were thus log-transformed (base 10) prior to analysis (Table 1).
Data stratification
The mean and standard deviation of all confounding factors, the treatment log TN, and the response invertebrate richness within all streams and within the three strata
Variable | Means ± standard deviation | |||
---|---|---|---|---|
All streams | Forested Mountains | Great Plains | North American Deserts | |
Log(TN) | 2.33 ± 0.51 | 2.04 ± 0.35 | 2.95 ± 0.36 | 2.64 ± 0.38 |
Invertebrate richness | 48.30 ± 15.15 | 55.19 ± 12.58 | 33.72 ± 11.76 | 40.03 ± 11.49 |
ELEV | 1252.06 ± 722.10 | 1455.84 ± 688.03 | 783.80 ± 379.71 | 1701.97 ± 501.16 |
Longitude | − 114.04 ± 7.55 | − 166.85 ± 5.48 | − 102.06 ± 3.16 | − 113.58 ± 4.06 |
Log(PRECIP) | − 0.31 ± 0.56 | − 0.07 ± 0.49 | − 0.81 ± 0.18 | − 0.74 ± 0.27 |
Log(AREA) | 4.07 ± 2.34 | 3.09 ± 1.68 | 6.77 ± 1.73 | 4.53 ± 2.56 |
Log(CL) | 4.35 ± 1.85 | 3.05 ± 1.20 | 6.04 ± 1.21 | 5.28 ± 1.73 |
Log(HCO3) | 7.34 ± 1.12 | 6.76 ± 1.06 | 8.44 ± 0.55 | 7.75 ± 0.77 |
Log(SO4) | 5.48 ± 2.42 | 3.97 ± 1.52 | 8.70 ± 1.61 | 6.42 ± 1.90 |
SED | 35.45 ± 30.35 | 1.82 ± 8.95 | 12.79 ± 32.54 | 4.85 ± 20.45 |
STRMTEMP | 15.16 ± 5.55 | 12.39 ± 4.19 | 20.58 ± 5.02 | 16.08 ± 5.70 |
Percent.AGT | 8.10 ± 21.28 | 0.58 ± 5.59 | 38.72 ± 33.44 | 2.90 ± 9.58 |
Percent.URB | 0.17 ± 0.47 | 0.06 ± 0.22 | 0.33 ± 0.44 | 0.13 ± 0.47 |
Percent.Canopy | 0.37 ± 0.38 | 0.23 ± 0.31 | 0.72 ± 0.32 | 0.59 ± 0.39 |
Riparian.Disturb | 0.56 ± 0.64 | 0.36 ± 0.57 | 1.10 ± 0.53 | 1.03 ± 0.56 |
An overview of statistical methods for causal inference
Implementation of the generalized propensity score
The generalized propensity score for each observation (i) is the probability density R_{ i } = r(T_{ i }, X_{ i }) (i.e., the likelihood of receiving treatment T_{ i }, given observed covariates X_{ i }), which was used to account for the aggregated effects of all the covariates in Eqs. (4) and (5). We emphasize here that the generalized propensity score is not the predicted treatment outcome, as in Eq. (2), but instead was the probability density of the residuals of the prediction, as in Eq. (3).
Verification of generalized propensity score
The generalized propensity score is a balancing score (Hirano and Imbens 2004; Imai and van Dyk 2004) when the model specification is appropriate. In other words, when observations are grouped into subsets with similar propensity scores, covariates within a subset should be similar among different treatment levels when the model used to derive the scores is appropriate. We use this expectation to verify the adequacy of the model specification. Hirano and Imbens (2004) proposed the use of a standardized difference to measure the balance in two steps. First, data were grouped into a number of categories (e.g., three) based on log TN (the treatment), each with roughly the same sample size. To show the balance in a confounding factor, we compare the means of the confounding factor among the three categories. The comparison can be made using a standardized difference, the difference of the means in the two categories divided by the standard error of the difference. The standard difference is similar to the t statistics in a two-sample t test. This comparison is first carried out directly to the data without GPS adjustment to illustrate the imbalance in the data. After calculating the propensity scores, we then divide the data into subsets of similar propensity scores and repeat the process of comparing confounding factors among three log TN categories within each relatively homogeneous subset of data. That is, in the second step, the data were divided into a number of subsets based on the calculated propensity scores (confounding factors are balanced within each subset), and within each subset, we further divide the data based on the treatment (log TN) to calculate the standardized mean differences of each confounding factor. The weighted averages of these standardized mean differences are known as the GPS-adjusted mean differences (Hirano and Imbens 2004). Weights of each subset are determined by the subset sample sizes. When the standardized differences of a confounding factor are between − 2 and 2, we consider that the confounding factor is balanced. Through comparing the change in the standardized differences calculated from the two steps, we can show the improvement in terms of confounding factor balance due to propensity score.
Comparison with regression without propensity score adjustment
We compared the dose-response estimation from the generalized propensity score to conventional regression models (without using propensity score adjustment). For the entire dataset, the Forested Mountains stratum and the North American Deserts stratum, we fitted generalized additive models (GAM) to compare with the generalized propensity score because of the nonlinear subsidy relationship. The selection of a smoothness parameter impacts the result of GAM. We used the default smoothness parameter in R package mgcv, which is determined based on a cross-validation simulation for optimal predictive features. The relationship was approximately linear for the Great Plains stratum. We thus fitted the simple linear and multiple linear regressions for comparison, which were then compared with the dose-response function estimated by generalized propensity score. 95% confidence zone of estimation from the generalized propensity scores was computed from a 1000 times bootstrap analysis. The statistical software used for all analyses was R version 3.24.
Results
Balancing check
Standardized mean differences between one group and the other two combined, using the entire dataset
Variable | Grouped by log TN (unadjusted) | Adjusted by GPS | ||||
---|---|---|---|---|---|---|
[1.17, 1.78] | [1.78, 2.69] | [2.69, 4.08] | [1.17, 1.78] | [1.78, 2.69] | [2.69, 4.08] | |
ELEV | − 1.33 | 6.88 | 6.68 | 0.32 | 2.40 | 1.57 |
Longitude | − 7.78 | − 7.07 | − 15.73 | − 1.94 | 0.51 | − 1.79 |
Log(PRECIP) | 12.06 | 2.98 | 13.20 | 0.79 | − 0.07 | 2.61 |
Log(AREA) | − 4.73 | − 7.02 | − 12.46 | − 1.85 | − 0.74 | − 0.76 |
Log(CL) | − 9.14 | − 5.40 | − 14.43 | − 1.88 | 1.47 | − 2.41 |
Log(HCO3) | − 9.28 | − 4.77 | − 13.59 | − 0.94 | − 1.52 | − 3.24 |
Log(SO4) | − 7.74 | − 8.00 | − 17.23 | − 0.76 | − 0.63 | − 4.16 |
SED | − 6.67 | − 8.77 | − 17.24 | − 1.76 | − 0.36 | − 2.33 |
STRMTEMP | − 6.67 | − 5.15 | − 11.72 | −0.64 | 0.26 | − 1.32 |
Percent.AGT | − 3.71 | − 12.21 | − 18.96 | − 1.15 | − 4.67 | − 7.54 |
Percent.URB | − 2.86 | − 2.91 | − 5.58 | 0.89 | 0.61 | − 0.55 |
Percent.Canopy | − 5.72 | − 5.40 | − 11.19 | − 1.72 | 0.56 | − 1.14 |
Riparian.Disturb | − 8.04 | − 3.88 | − 11.15 | 1.11 | 0.60 | − 1.85 |
Standardized mean differences between one group and the other two combined for the Forested Mountains ecoregion stratum
Variable | Grouped by log TN (unadjusted) | Adjusted for the GPS | ||||
---|---|---|---|---|---|---|
[1.17, 1.60] | [1.60, 2.44] | [2.44, 3.74] | [1.17, 1.60] | [1.60, 2.44] | [2.44, 3.74] | |
ELEV | − 2.73 | 0.74 | − 1.53 | − 0.49 | 0.57 | 1.29 |
Longitude | − 3.43 | 0.36 | − 2.65 | − 0.51 | 0.43 | 1.15 |
Log(PRECIP) | 5.12 | − 0.16 | 4.41 | 0.63 | − 0.93 | − 0.28 |
Log(AREA) | − 1.56 | 0.24 | − 1.12 | 0.44 | − 0.72 | 0.89 |
Log(CL) | − 2.81 | − 3.42 | − 7.35 | − 1.01 | − 0.95 | − 3.39 |
Log(HCO3) | − 3.62 | − 0.69 | − 4.22 | − 0.64 | − 1.09 | − 0.29 |
Log(SO4) | − 3.26 | − 0.13 | − 3.13 | − 1.61 | − 0.44 | − 0.36 |
SED | 0.54 | − 1.61 | − 1.56 | − 0.06 | − 1.34 | 0.03 |
STRMTEMP | − 2.30 | 0.22 | − 1.80 | − 0.21 | − 0.50 | 0.57 |
Percent.AGT | − 0.60 | − 1.90 | − 2.98 | − 0.23 | 0.34 | − 5.56 |
Percent.URB | − 0.74 | − 2.21 | − 3.53 | 0.26 | − 0.16 | − 6.47 |
Percent.Canopy | − 1.41 | − 2.37 | − 4.40 | − 0.99 | − 0.14 | − 1.32 |
Riparian.Disturb | − 3.43 | − 2.41 | − 6.50 | − 1.64 | − 1.21 | − 1.52 |
Standardized mean differences between one group and the other two combined for the Great Plains ecoregion
Grouped by log TN (unadjusted) | Adjusted for the GPS | |||||
---|---|---|---|---|---|---|
Variable | [2.05, 2.56] | [2.56, 3.19] | [3.19, 4.08] | [2.05, 2.56] | [2.56, 3.19] | [3.19, 4.08] |
ELEV | 7.45 | − 1.37 | − 9.02 | 1.85 | 0.30 | 0.91 |
Longitude | − 5.37 | − 0.05 | − 3.92 | − 1.65 | 0.98 | − 2.14 |
Log(PRECIP) | 3.15 | − 2.94 | − 0.87 | 2.08 | − 2.17 | − 1.39 |
Log(AREA) | − 3.46 | 2.02 | − 0.29 | − 1.63 | 1.89 | 1.22 |
Log(CL) | 0.63 | − 1.31 | − 0.96 | 0.69 | − 1.48 | − 1.42 |
Log(HCO3) | − 4.67 | 1.04 | − 2.13 | − 1.55 | 0.19 | − 0.98 |
Log(SO4) | − 2.22 | 0.11 | − 1.53 | 0.45 | − 0.37 | − 0.46 |
SED | 0.07 | − 2.21 | − 2.41 | 2.38 | − 1.41 | − 2.08 |
STRMTEMP | − 3.59 | 0.99 | − 1.49 | − 1.50 | 0.26 | − 0.81 |
Percent.AGT | − 4.05 | − 0.78 | − 3.98 | − 0.52 | − 1.13 | − 1.87 |
Percent.URB | 1.05 | − 1.62 | − 0.99 | 0.21 | − 1.80 | − 1.74 |
Percent.Canopy | 0.16 | 0.20 | 0.35 | − 0.14 | 0.39 | 1.05 |
Riparian.Disturb | − 2.36 | 2.19 | 0.65 | − 1.52 | 1.83 | 0.98 |
Standardized mean differences between one group and the other two combined for the North American ecoregion
Variable | Unadjusted | Adjusted for the GPS | ||||
---|---|---|---|---|---|---|
[1.77, 2.35] | [2.35, 2.69] | [2.69, 3.80] | [1.77, 2.35] | [2.35, 2.69] | [2.69, 3.80] | |
ELEV | 1.24 | − 1.95 | − 0.71 | 0.74 | − 2.57 | 0.14 |
Longitude | 0.35 | − 0.64 | − 0.30 | 0.77 | − 0.57 | − 0.95 |
Log(PRECIP) | 2.82 | 0.27 | 3.10 | 0.79 | 0.52 | 2.28 |
Log(AREA) | − 1.23 | 2.17 | 0.93 | − 0.62 | 1.99 | 1.95 |
Log(CL) | − 3.75 | 1.30 | − 2.23 | − 2.35 | 1.53 | − 1.89 |
Log(HCO3) | − 0.65 | − 0.71 | − 1.37 | 1.08 | − 1.05 | − 0.89 |
Log(SO4) | − 1.66 | 0.87 | − 0.75 | 0.59 | 1.31 | − 1.17 |
SED | − 1.21 | − 0.67 | − 1.90 | − 1.49 | − 0.23 | − 1.66 |
STRMTEMP | − 2.69 | 2.35 | − 0.27 | − 2.03 | 1.71 | 1.38 |
Percent.AGT | − 0.89 | − 1.35 | − 2.29 | − 0.43 | − 1.59 | − 3.11 |
Percent.URB | − 0.94 | 1.11 | 0.19 | − 0.61 | 2.55 | − 0.73 |
Percent.Canopy | − 1.11 | − 0.31 | − 1.43 | − 0.72 | − 0.66 | − 1.05 |
Riparian.Disturb | − 1.02 | 0.22 | − 0.79 | 0.72 | 0.57 | 0.56 |
Dose-response relationship
Comparison with direct regressions
At medium to very high N concentrations, the estimation from GAM for the full set of streams was different from the dose-response estimation by the generalized propensity score (Fig. 4). However, among the three sub-ecoregions, the difference between the direct regression and the generalized propensity score (Fig. 5) is smaller than the difference shown in Fig. 4. In the Northwestern Forested Mountains stratum, GAM had fit a subsidy-stress relationship that was only slightly outside the 95% confidence zone of the generalized propensity score estimation when within the middle ranges of N concentration (Fig. 5a). For the North American Deserts stratum, the GAM fit completely within the 95% confidence zone of the generalized propensity score (Fig. 5c). For the Great Plains stratum, the fitted lines from both the simple and multiple linear regressions closely followed the mean estimation of the generalized propensity score (Fig. 5b).
Discussion
On average, benthic invertebrate richness in streams within the 12 western states of the USA exhibits a subsidy-stress relationship with total nitrogen. This result is consistent with the conclusion that a high level of nutrient concentrations negatively affects invertebrate richness in streams, a conclusion also found in manipulative experiments and observational studies (Tilman 1987; Dodson et al. 2000; Haddad et al. 2000; Wang et al. 2007). Yuan (2010) studied the same data from the EPA by stratifying the data into different groups based on predicted log(TN) concentrations from its covariates instead of the propensity score. The six groups essentially represent different N concentration ranges. Yuan’s (2010) observed increases in TN were associated with small increases in IR in the first three groups (low nutrient levels) and a significantly negative correlation between log TN and IR in the last three groups (high nutrient levels), suggesting that there is a subsidy-stress relationship. The average subsidy-stress relationship found over a large region also explains why conflicting results (e.g., no correlation, positive and negative association) have been found in small areas. When streams in a small area have limited nutrients, increases in nutrients can lead to increase in periphyton biomass, which can support a greater diversity of invertebrates (Chetelat et al. 1999); therefore, only positive correlations could be observed. On the other hand, when nutrients are excessive in a stream, the diminished water quality and the depleted oxygen caused by decomposition of periphyton biomass will likely reduce IR (Correll 1998), leading to a negative association between nutrients and IR.
Although the same subsidy-stress relationship was found in the three ecoregions we studied, the variation among regions is also obvious. At a similar nutrient level, streams in different ecoregions have different expected IR (Fig. 5), as nutrient enrichment is only one of the many factors that may influence the diversity of the stream macroinvertebrate community (Wang et al. 2007; Yuan 2010). The generalized propensity score produces an average dose-response function that is controlled by the average condition represented in the data. The three strata in our study have different covariate mean values (Table 2), representing differences in natural conditions and anthropogenic activities; the differences in these conditions and activities contribute to the variability in both the observed nutrient concentrations and the TN-IR relationship. For example, both local- and catchment-scale disturbances can reduce stream macroinvertebrate taxon richness (Ligeiro et al. 2013). The Great Plains ecoregion has the highest percentage of agricultural and urban areas and riparian disturbance. This stratum thus has the lowest IR, even for streams at comparable TN levels with streams in other strata. The characteristics of flow regimes affected by precipitation events are widely recognized as important variables in determining the diversity and community composition in streams (Resh et al. 1988; Poff et al. 1997). Different precipitation patterns in the three ecoregions can produce totally different flow regimes (David 2006) that may change the nutrient-IR relationship (Palardy and Witman 2010). Higher temperatures in the North American Deserts can also increase stream temperature, changing sediments, and dissolved oxygen (Darren et al. 2013) which may increase the excessive nutrient stress to IR (USEPA 1996). Similar effects of other covariates on IR and nutrients may also occur.
The detrimental effects of excess nutrients require controls on nutrient loadings to streams based on nutrient effects (Dodds and Welch 2000). Our study provides practical guidance on how to find a scientifically defensible threshold value of TN (e.g., the breaking point log (TN) in Fig. 3b) that will result in no detectable harmful effect on IR. If confounding effects were not approximately controlled, the resulting biased estimate of the causal effect would lead to a biased threshold value. It is therefore important to have reliable estimates of causal effects. The same approach and principle can be applied to other pollutants and ecological indicators. However, as varying natural and anthropogenic conditions exist in different regions, nutrient effects are stream- or region-specific (Fig. 5). As a result, nutrient thresholds for setting environmental standards need to be region/area-specific to increase their value for application. For example, a nationwide nutrient threshold might be higher for some states/provinces but lower for other states/provinces, and the same problem can be extended to different counties within a state/province. However, in practice, the sample size may be limited when the area of targeted regions becomes small, which may increase the uncertainty associated with dose-response estimation. The value of larger-scale studies like the current study can be realized under a Bayesian framework, where an informative prior distribution of the TN effect can be derived (Gelman and Hill 2007). This use of the Bayesian approach is consistent with the interpretation of a Bayesian prior distribution representing the among-site variability (Qian et al. 2015). Local agencies can establish a process whereby they gradually update the dose-response function when new region-specific data are available. This Bayesian updating approach will gradually move from the larger scale average dose-response relationship towards a locally region-specific dose-response relationship.
An important assumption of the generalized propensity score approach is the “weak unconfoundedness” assumption, which states that all important confounding factors are included in the treatment assignment model (i.e., Eqs. (3) and (4)). This assumption suggests that we should collect as many covariates as possible when designing an observational study to guard against missing any important confounding factors. We have identified and included all important confounders available from the wadeable stream assessment dataset, which was created by the EPA (Table 1). However, we may have missed some potentially important confounding factors that were not observed, such as site history and variability of flow velocity. Nevertheless, we have controlled some of the potential covariates and strengthened the estimation of the nutrient’s causal effect on invertebrate richness. Many unobserved confounding factors are likely to be correlated with these observed covariates and are thus partially controlled for as well.
When we started this study, we expected that the dose-response relationship estimated by GPS would be different from that estimated by linear regression and GAM. The difference is indeed obvious when comparing the two estimated dose-relationships using the entire dataset (Fig. 4, top panel). However, the differences were not obvious when we repeated the same modeling approaches in the three ecoregion-based strata. When using the entire dataset, confounding factors are highly imbalanced. This imbalance is shown in the large (absolute value) standardized mean differences of all confounding factors (Table 3). Such imbalances are, however, not as pronounced in the data within the three ecoregion-based strata (Tables 4, 5, and 6). As a result, ecoregion-based dose-response relationships are relatively similar, with or without GPS adjustment. This result highlights the regional differences in the dose-response relationship, which suggests the value of region-specific nutrient criteria.
Conclusions
The regional average of nutrient causal effects on stream invertebrate richness was estimated using observational data, with confounding effects controlled for using the generalized propensity score. The aggregated confounding effects were removed by integration through the single propensity score. We found a subsidy-stress relationship between nutrients and invertebrate taxon richness across streams both in the Western United States and its sub-regions. This same general pattern varies among ecoregions due to the varying natural conditions and anthropogenic activities. The variation demonstrated that invertebrates respond to the same nutrient levels differently across different conditions.
Declarations
Acknowledgements
We thank Lester Yuan from the National Center for Environmental Assessment, Office of Research and Development, and the US Environmental Protection Agency for providing the necessary data. We also thank Janet Traub, Gabriela Shirkey, and Connor Crank Huffman for proof-reading the text. Comments and suggestions from the reviewers and the associate editor are greatly appreciated.
Funding
The first author receives financial support from the National Aeronautics and Space Administration (NASA)’s Land Cover and Land Use Program through their grant to Michigan State University (NNX15AD51G).
Availability of data and materials
The data and code for estimating the causal effects of nitrogen on invertebrate richness for the 12 western US states are available through the first author’s GitHub page (https://github.com/ouyangzt/Generalized-propensity-score).
Authors’ contributions
ZY and SQ designed the study. ZY performed the data analysis including the necessary calculations and statistics analysis. ZY, SQ, JC, and RB wrote the manuscript. RB assisted in the data analysis, and JC provided editorial assistance. All authors read and approved the final manuscript.
Competing interests
The authors declare that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
Authors’ Affiliations
References
- Bergfur J, Johnson RK, Sandin L, Goedkoop W, Nygren K (2007) Effects of nutrient enrichment on boreal streams: invertebrates, fungi and leaf-litter breakdown. Freshw Biol 52:1618–1633View ArticleGoogle Scholar
- Blair R (2001) Environmental monitoring and assessment program: west-research strategy. U.S. Environmental Protection Agency, Washington, D.C.Google Scholar
- Chetelat, J, Pick, FR, Morin, A, Hamilton, PB (1999) Periphyton biomass and community composition in rivers of different nutrient status. Can J Fish Aquat Sci 56: 560–569.View ArticleGoogle Scholar
- Clenaghan C, Giller PS, O’halloran J, Hernan R (1998) Stream macroinvertebrate communities in a conifer-afforested catchment in Ireland: relationships to physico-chemical and biotic factors. Freshw Biol 40:175–193View ArticleGoogle Scholar
- Correll DL (1998) The role of phosphorus in the eutrophication of receiving waters: a review. J Environ Qual 27:261–266View ArticleGoogle Scholar
- Cross WF, Wallace JB, Rosemond AD, Eggert SL (2006) Whole-system nutrient enrichment increases secondary production in a detritus-based ecosystem. Ecology 87:1556–1565View ArticleGoogle Scholar
- Darren LF, Iris TS, Edwin PM (2013) Effects of climate change on stream temperature, dissolved oxygen, and sediment concentration in the Sierra Nevada in California. Water Resour Res 49:2765–2782View ArticleGoogle Scholar
- David S (2006) Trends in precipitation and streamflow in the eastern U.S.: paradox or perception? Geophys Res Lett 33:L03403Google Scholar
- Dodds WK, Welch EB (2000) Establishing nutrient criteria in streams. J N Am Benthol Soc 19:186–196View ArticleGoogle Scholar
- Dodson SI, Arnott SE, Cottingham KL (2000) The relationship in lake communities between primary productivity and species richness. Ecology 81:2662–2679View ArticleGoogle Scholar
- Elser JJ, Bracken MES, Cleland EE, Gruner DS, Harpole WS, Hillebrand H, Ngai JT, Seabloom EW, Shurin JB, Smith JE (2007) Global analysis of nitrogen and phosphorus limitation of primary producers in freshwater, marine and terrestrial ecosystems. Ecol Lett 10:1135–1142View ArticleGoogle Scholar
- Fisher RA (1966) The design of experiment, 6th edn. Oliver and Boyd Ltd, LondonGoogle Scholar
- Fore LS, Karr JR, Wisseman RW (1996) Assessing invertebrate responses to human activities: evaluating alternative approaches. J N Am Benthol Soc 15:212–231View ArticleGoogle Scholar
- Francoeur SN (2001) Meta-analysis of lotic nutrient amendment experiments: detecting and quantifying subtle responses. J N Am Benthol Soc 20:358–368View ArticleGoogle Scholar
- Freeman AM, Lamon Iii EC, Stow CA (2009) Nutrient criteria for lakes, ponds, and reservoirs: a Bayesian TREED model approach. Ecol Model 220:630–639View ArticleGoogle Scholar
- Gafner K, Robinson CT (2007) Nutrient enrichment influences the responses of stream macroinvertebrates to disturbance. J N Am Benthol Soc 26:92–102View ArticleGoogle Scholar
- Gelman A, Hill J (2007) Data analysis using regression and multilevel/hierarchical models. Cambridge University Press, New YorkGoogle Scholar
- Gulis V, Suberkropp K (2004) Effects of whole-stream nutrient enrichment on the concentration and abundance of aquatic hyphomycete conidia in transport. Mycologia 96:57–65View ArticleGoogle Scholar
- Haddad NM, Haarstad J, Tilman D (2000) The effects of long-term nitrogen loading on grassland insect communities. Oecologia 124:73–84View ArticleGoogle Scholar
- Harding JS, Young RG, Hayes JW, Shearer KA, Stark JD (1999) Changes in agricultural intensity and river health along a river continuum. Freshw Biol 42:345–357View ArticleGoogle Scholar
- Hart DD, Robinson CT (1990) Resource limitation in a stream community: phosphorus enrichment effects on periphyton and grazers. Ecology 71:1494–1502View ArticleGoogle Scholar
- Heino J, Muotka T, Paavola R (2003) Determinants of macroinvertebrate diversity in headwater streams: regional and local influences. J Anim Ecol 72:425–434View ArticleGoogle Scholar
- Hirano, K. and G. W. Imbens. 2004. The propensity score with continuous treatments. Missing data and Bayesian methods in practice: contributions by Donald Rubin’s statistical familyGoogle Scholar
- Imai K, van Dyk DA (2004) Causal inference with general treatment regimes: generalizing the propensity score. J Am Stat Assoc 99:854–866View ArticleGoogle Scholar
- Ligeiro R, Hughes RM, Kaufmann PR, Macedo DR, Firmiano KR, Ferreira WR, Oliveira D, Melo AS, Callisto M (2013) Defining quantitative stream disturbance gradients and the additive role of habitat variation to explain macroinvertebrate taxa richness. Ecol Indic 25:45–57View ArticleGoogle Scholar
- Maldonado G, Greenland S (2002) Estimating causal effects. Int J Epidemiol 31:422–429View ArticleGoogle Scholar
- Moss D, Furse MT, Wright JF, Armitage PD (1987) The prediction of the macro-invertebrate fauna of unpolluted running-water sites in Great Britain using environmental data. Freshw Biol 17:41–52View ArticleGoogle Scholar
- Niyogi DK, Koren M, Arbuckle CJ, Townsend CR (2007) Stream communities along a catchment land-use gradient: subsidy-stress responses to pastoral development. Environ Manag 39:213–225View ArticleGoogle Scholar
- Omernik JM (1987) Ecoregions of the conterminous United States. Ann Assoc Am Geogr 77:118–125View ArticleGoogle Scholar
- Palardy JE, Witman JD (2010) Water flow drives biodiversity by mediating rarity in marine benthic communities. Ecol Lett 14:63–68View ArticleGoogle Scholar
- Poff NL, Allan JD, Bain MB, Karr JR, Prestegaard KL, Richter BD, Sparks RE, Stromberg JC (1997) The natural flow regime. Bioscience 47:769–784View ArticleGoogle Scholar
- Qian SS, Harmel RD (2016) Applying statistical causal analyses to agricultural conservation: a case study examining P loss impacts. J Am Water Resour Assoc 52:198–208View ArticleGoogle Scholar
- Qian SS, Stow CA, Cha Y (2015) Implications of Stein’s paradox for environmental standard compliance assessment. Environ Sci Technol 49:5913–5920View ArticleGoogle Scholar
- Quinn JM, Cooper AB, Stroud MJ, Burrell GP (1997) Shade effects on stream periphyton and invertebrates: an experiment in streamside channels. N Z J Mar Freshw Res 31:665–683View ArticleGoogle Scholar
- Resh VH, Brown AV, Covich AP, Gurtz ME, Li HW, Minshall GW, Reice SR, Sheldon AL, Wallace JB, Wissmar RC (1988) The role of disturbance in stream ecology. J N Am Benthol Soc 7:433–455View ArticleGoogle Scholar
- Rosemond AD, Mulholland PJ, Elwood JW (1993) Top-down and bottom-up control of stream periphyton—effects of nutrients and herbivores. Ecology 74:1264–1280View ArticleGoogle Scholar
- Rosenbaum PR, Rubin DB (1983) The central role of the propensity score in observational studies for causal effects. Biometrika 70:41–55View ArticleGoogle Scholar
- Rubin DB (2006) Matched sampling for causal effects. Cambridage University Press, CambridageView ArticleGoogle Scholar
- Slavik K, Peterson BJ, Deegan LA, Bowden WB, Hershey AE, Hobbie JE (2004) Long-term responses of the Kuparuk River ecosystem to phosphorus fertilization. Ecology 85:939–954View ArticleGoogle Scholar
- Smith VH, Tilman GD, Nekola JC (1999) Eutrophication: impacts of excess nutrient inputs on freshwater, marine, and terrestrial ecosystems. Environ Pollut 100:179–196View ArticleGoogle Scholar
- Stoddard JL, Peck DV, Olsen AR, Larsen DP, Sickle JV, Hawkins CP, Hughes RM, Whittier TR, Lomnicky G, Herlihy AT, Kaufmann PR, Peterson SA, Ringold PL, Paulsen RBSG (2006) Environmental monitoring and assessment (EMAP) western streams and rivers statistical summary. Office of Research and Development, U.S. Environmental Protection Agency, Washington, D.C.Google Scholar
- Tilman D (1987) Secondary succession and the pattern of plant dominance along experimental nitrogen gradients. Ecol Monogr 57:189–214View ArticleGoogle Scholar
- USEPA (1996) National Nutrient Assessment Workshop Proceedings, EPA-822-96-004. Office of Water, US Environmental Protection Agency, Washington, DCGoogle Scholar
- USEPA (2000) Nutrient criteria technical guidance mannual: rivers streams. Office of Water, Office of Science and Technology, Washington, DCGoogle Scholar
- Wang L, Robertson D, Garrison P (2007) Linkages between nutrients and assemblages of macroinvertebrates and fish in wadeable streams: implication to nutrient criteria development. Environ Manag 39:194–212View ArticleGoogle Scholar
- Yuan LL (2010) Estimating the effects of excess nutrients on stream invertebrates from observational data. Ecol Appl 20:110–125View ArticleGoogle Scholar