Translator Disclaimer
29 September 2010 Thresholds, breakpoints, and nonlinearity in freshwaters as related to management
Author Affiliations +

Nonlinear ecological responses to anthropogenic forcing are common, and in some cases, the ecosystem responds by assuming a new stable state. This article is an overview and serves as the introduction to several articles in this BRIDGES cluster that are directed toward managers interested in dealing with nonlinear responses in freshwaters, particularly streams. A threshold or breakpoint occurs where the system responds rapidly to a relatively small change in a driver. The existence of a threshold can signal a change in system configuration to an alternative stable state, although such a change does not occur with all thresholds. In general, a mechanistic understanding of ecological dynamics is required to predict thresholds, where they will occur, and if they are associated with the occurrence of alternative stable states. Thresholds are difficult to predict, although a variety of univariate methods has been used to indicate thresholds in ecological data. When we applied several methods to one type of response variable, the resulting threshold values varied 3-fold, indicating that more research on detection methods is necessary. Numerous case studies suggest that the threshold concept is important in all ecosystems. Managers should be aware that human actions might result in undesirable rapid changes and potentially an unwanted alternative stable state, and that recovery from that state might require far more resources and time than avoiding entering the state in the first place would have required. Given the difficulties in predicting thresholds and alternative states, the precautionary approach to ecosystem management is probably the most prudent.

The scientific and popular literature are full of examples of rapid and sometimes catastrophic ecological change caused by what initially were thought to be benign and relatively small change(s) in the environment. Internal feedbacks can lead to multiple stable states in ecosystems (Dent et al. 2002, Wootton 2010), and often these state changes are caused by anthropogenic factors. Examples include major changes in community structure and biogeochemistry of lakes subjected to nutrient pollution (Carpenter 2003), strong but delayed responses to nutrient addition in an arctic river (Slavik et al. 2004), decades-long lags in stream macroinvertebrate responses to watershed disturbance (Harding et al. 1998), shift to vegetation stabilization of substrates in streams following removal of terrestrial grazing pressure (Heffernan 2008), and shift to a flood-resistant algal and macroinvertebrate community following restoration of natural flood conditions (Robinson and Uehlinger 2008).

The ideas of potential instability and catastrophic change have existed in biological (Thom 1972) and ecological thought (e.g., May 1977) for decades. However, the concept of abrupt changes to alternative stable states has received considerable and warranted attention recently. A paper by Scheffer et al. (2001) on catastrophic shifts in ecosystems had been cited >1000 times by mid 2009. Analysis of Institute of Scientific Information (ISI) Web of Science citations indicates that the number of papers using the topics “ecological threshold” or “alternative stable state” coupled with “ecolo*” has climbed sharply every 5-y period since 1990 until the writing of this article (Fig. 1A). The percentage increase was substantially greater than the increase in articles with the topic “ecolo*” alone (Fig. 1B). This simple analysis indicates that the ideas of ecological thresholds and alternative stable states are receiving strong research interest and that managers might be helped by information on this relevant and rapidly developing area of ecology.

Figure 1

Search results of number of citations from Institute of Scientific Information (ISI) Web of Science for the 3 topics: 1) ecological threshold, 2) alternative stable state and ecolo* and 3) ecolo*, where the * represents a character string wildcard. A.—Searching defined ranges of years for the 3 topics. B.—Results presented as a percentage of 1990 to 1994 citations to control for the increase in general ecology articles (ecolo*). Note the search was conducted in July 2009, so the last range of dates is truncated.


Predicting thresholds is important because they can influence ecosystem goods and services that people value (Martin et al. 2009). Recovery from a shift to an alternative stable state might not occur until stressor levels are reduced significantly (Bellwood et al. 2004, Hughes et al. 2005). Thus, identifying potential thresholds is an important aspect of managing ecological systems. Predictive understanding is central to applying ecology (Dodds 2009). Unfortunately, we cannot predict such changes well enough to manage many ecosystems adequately (Scheffer et al. 2009). How are managers of freshwater ecosystems to deal with the idea that systems can change abruptly in ways that do not mirror past patterns? Groffman et al. (2006) acknowledged that such abrupt changes are of interest to all ecologists, that the concept can be useful, but that much is not understood about how to apply the idea of abrupt change to management. For example, feedbacks leading to alternate states might be more common in lakes than in rivers (Dent et al. 2002), but this hypothesis has not been tested, and poor management decisions could arise from the assumption that the statement is an accurate generalization (not the intent of the paper by Dent et al. 2002). The papers in this BRIDGES cluster (Clements et al. 2010, Hilderbrand et al. 2010, King and Baker 2010) and another paper in this issue (Gido et al. 2010) illustrate advances in detecting thresholds and their consequences in streams.

The aims of our paper are to: 1) define and organize common terms, 2) collate and apply some methods with promise for identifying thresholds, 3) review illustrative examples of thresholds and alternative stable states from aquatic systems, and 4) establish how mechanistic understanding coupled with detection of thresholds could be of use to managers. This paper also serves as an introduction to the BRIDGES cluster, which aims to demonstrate different analytical methods to detect thresholds, highlight evidence of degradation and recovery thresholds in streams, and discuss implications of nonlinear response patterns to management of aquatic ecosystems.

Definition of Terms Related to Thresholds and Alternative Stable States

Groffman et al. (2006) defined an ecological threshold as the point at which an abrupt change occurs in an ecological quality, property, or phenomenon or where small changes in a driver produce large responses in the ecosystem (see Table 1 for a list of definitions of relevant terms used in our paper). Here, we assume the driver is an abiotic or biotic change over time or space that influences ecological state. In some cases, time or space can be used as a proxy for the change in the driver and to account for lags in response to drivers. Threshold does not refer to the form of the function, which could be a step, an abrupt but continuous change in a functional relationship to a different equation, or a property of a single equation. Breakpoint often is used interchangeably with threshold, but usually refers to a place or time at which a sharp jump occurs from one function to another (a step function).

Table 1

Definitions of overarching terms associated with ecological thresholds used in this paper.


Species area curves, N saturation of rivers, fragmentation of stream networks (Fagan et al. 2002), patch size and extinction risk, biotic responses to contaminants, and altered thermal regimes are all examples of nonlinear responses. However, nonlinearity does not necessarily indicate that a specific threshold exists. Nonlinearities can be difficult to distinguish from thresholds in real-world data, but thresholds can indicate movement to an alternative stable state and a specific point of which managers should be aware, whereas many nonlinear relationships yield no specific natural breakpoint or threshold.

We provide 2 examples of nonlinearity that are not profitably viewed as a threshold. First, consider regular oscillations of an ecosystem property, perhaps approximated by a sine wave. If we observe only a single trough and peak, we could assume a threshold shift. A longer time series would reveal the regular oscillations. Second, consider the example of the Michaelis–Menten relationship for enzyme activity (Dodds et al. 1991). The function can roughly describe mechanism of nutrient uptake of microbial assemblages (Williams 1973). When data from this equation are viewed graphically, they could be equally well represented by 2 straight lines or by the Michaelis–Menten function (Fig. 2A vs 2B). However, the continuous nature of these data becomes more obvious at lower nutrient concentrations (∼0.6 nM NH4+) (Fig. 2C). In both these examples, defining the nonlinear pattern as a threshold incorrectly characterizes the known nature of the systems.

Figure 2

Relationship between NH4+ concentration and uptake for Flathead Lake phytoplankton based on piecewise linear fit (adjusted r2  =  0.92) (A), Michaelis–Menten fit (adjusted r2  =  0.92) (B), and the lower portion of the Michaelis–Menten curve expanded (C). Data from Dodds et al. (1991).


Thresholds or breakpoints often are linked to alternative stable states. However, the existence of a threshold does not dictate the presence of mechanisms that would maintain an alternative stable state after the threshold is crossed. Stable states can be defined mathematically (e.g., community matrices where all eigenvalues have negative real parts, Lyapunov stability; May 1973) or conceptually (under conditions where strict mathematical definition is difficult, not possible, or not necessary).

The concept of an alternative stable state can be presented simply (e.g., a ball on a 2- or 3-dimensional landscape with local minima; Gunderson 2000). However, the actuality of stable states in ecological systems is more complex (Pawlowski 2006), and establishing their existence in the context of ecological management can be difficult and can depend on temporal and spatial scale. For example, alternative stable states exist when shallow lakes or ponds can be dominated by either macrophytes or phytoplankton (Carpenter 2003), but both of these states are ephemeral with respect to the fact that the pond will fill over geological time scales. Movement of a system from one state to another also has been defined as a regime shift (Andersen et al. 2009). Ecological regime has been defined as synonymous to alternative stable state (Mayer and Rietkerk 2004), but the definition of ecological regime provided by Anderson et al. (2009) does not specifically require that the alternative state be stable. Here, we use the term alternative state and indicate if it is a stable state, and we avoid referring to ecological regimes.

Methods for Fitting Nonlinear Ecological Relationships

Numerous methods can be used to find thresholds and characterize nonlinearity between a variable describing ecological state and a driver gradient or temporal trend (e.g., Brenden et al. 2008, Andersen et al. 2009; Table 2). Some thresholds, such as losing a species to extinction, paving a meadow, or drying a stream channel, are so obvious that no statistics are needed. In other cases, graphing the data is a good first step and is useful for checking statistical results (Brenden et al. 2008). We know of only 2 published studies in which suitability of various methods was tested by application to the same data. Results from 2-dimensional Kolmogorov–Smirnov testing and breakpoint regression were in general agreement on thresholds in a very limited study of the relationship between stream nutrients and benthic algal biomass (Dodds et al. 2002). Brenden et al. (2008) used simulated univariate response data to test for thresholds in a step function, a decrease, and a data wedge. They found that a quantile piecewise linear approach (a form of regression tree analysis) was the most robust method, but they did not evaluate uncertainty (e.g., confidence limits around thresholds, variability, and capture rate of simulated thresholds).

Table 2

Some methods for identifying nonlinear and threshold relationships. D1  =  detection limit of the method, T95  =  region with 95% certainty of change.


We subjected data on the relationship between total P and stream macroinvertebrate richness to additional methods (see references in Table 2 for analytical details). All methods agreed that a threshold concentration of nutrients existed above which macroinvertebrate diversity declined less rapidly. The concentration of total P at which the threshold occurred was similar across methods, but some methods differed as much as 3-fold in their threshold estimates (Table 3, Figs 3A, 4A–C). Because some methods lacked confidence limits or other measures of uncertainty, threshold estimates could not be compared rigorously among methods. A more extensive approach, such as that applied by Brenden et al. (2008), but using a greater variety of methods and measures of uncertainty with real and simulated data would be necessary to evaluate which method works best on specific types of data.

Figure 3

Breakpoint regression analysis of macroinvertebrate consumer (A) and predator (B) richness as a function of water-column total P (TP) from 237 US Central Plains stream sites across Kansas, Nebraska, and Missouri in spring and autumn (data from Evans-White et al. 2009).


Figure 4

Macroinvertebrate consumer richness represented as the cumulative percentage of cases with <30 primary consumer species (A), quantile regression splines (B), and nonparametric changepoint analysis cumulative threshold frequency (C) as a function of water-column total P (TP) from 237 US Central Plains stream sites across Kansas, Nebraska, and Missouri in spring and autumn (data from Evans-White et al. 2009).


Table 3

Breakpoints or thresholds in the relationship between macroinvertebrate richness and total P determined using various methods applied to data presented in Figs 3A, 4A–C. For reference to method used, see Table 2. Confidence interval in piecewise regression was Bonferroni corrected. – indicates method unable to calculate parameter. SiZer  =  significant zero crossings.


Some methods are better suited for specific data types. Time series are particularly important in understanding thresholds (Andersen et al. 2009). For example, responses of state variables can be expressed as a function of time since restoration of a system. Sonderegger et al. (2009) developed a derivative-based, nonparametric approach to detect ecological thresholds in long-term data sets. The significant zero crossings (SiZer) approach was used to quantify recovery of benthic communities following improvements in water quality (Clements et al. 2010) and was useful to distinguish long-term (11 y) recovery threshold from shorter-term climatic variation.

Methods that could detect thresholds before they are crossed would be most useful to managers. Prediction might be possible because thresholds are associated with a rise in variance as the threshold is approached (Carpenter et al. 2008), and an increase in autocorrelation between a response variable and a driver or time can occur (Scheffer et al. 2009). However, these ideas have not been broadly tested, and their use might be complicated because variance can increase with the length of the time series (Halley 1996). Knowledge of an impending threshold and resulting regime shift would be valuable for maintaining ecosystem condition, but the temptation could be to try to manage the system up to the threshold in an effort to optimize the system. Given uncertainties in our ability to estimate thresholds, this approach could provide a false sense of security that the system is below the ecological threshold.

The Importance of Defining Mechanism

In addition to the challenges associated with empirical methods used to detect thresholds, field methods, experiments, and models used to demonstrate the existence of alternative stable states are accompanied by challenges. Scheffer and Carpenter (2003) state that it is “remarkably difficult to prove the existence of alternative attractors in the field”. The challenges of predicting change are exacerbated by the fact that global geochemical, geophysical, and biological changes are leading to unprecedented biotic (Fox 2007, Williams and Jackson 2007, Dodds 2008, Jelks et al. 2008) and hydrologic (Milly et al. 2008) conditions. Extrapolation from empirical relationships (e.g., Peters 1991) will be complicated because the context of these relationships will have changed.

Thus, understanding specific mechanisms that control the state of a system is essential to increase our ability to understand what would alter the system or return it to its initial state and to predict thresholds (Dodds 2009). Consider again the Michaelis–Menten relationship (Fig. 2A–C). The empirically fitted breakpoint offers no mechanism to predict the ability of microorganisms to take up NH4+ after chronic fertilization. However, our understanding of nutrient uptake by enzymes and biological tradeoffs suggests that maximum uptake should increase and uptake at lower concentrations should decrease. Our ability to predict the functional relationships among nutrient loading, uptake, and retention depends on understanding the mechanisms driving nutrient uptake (O'Brien et al. 2007) and has specific relevance to managers concerned with ecosystem responses to chronic and acute nutrient pollution (O'Brien and Dodds 2010).

Two of the most commonly cited cases of thresholds and alternative stable states are found in lakes. In both cases, clear understanding of mechanisms aids in management. 1) Dissolution of iron phosphate in anoxic conditions that develop in hypolimnia of eutrophic lakes leads to high rates of internal P loading and a very stable eutrophic state that is insensitive to decreases in external nutrient loading (Carpenter et. al. 1999). The chemical mechanism is well understood, and the implication for managers is that allowing a lake to become so eutrophic that anoxic conditions develop will make restoring the lake extremely difficult. 2) Shallow lakes can be dominated either by phytoplankton or macrophytes. Foodweb manipulation can reduce phytoplankton shading and increase macrophytes, and increased macrophytes can produce allelochemicals that reduce phytoplankton growth rates and maintain clear water (Dent et al. 2002). The mechanism is biotic and revolves around competition for light and ability of macrophytes to produce allelochemicals. The implication for management is that removing all macrophytes from a shallow lake could cause unwanted phytoplankton blooms.

In streams, the relationship between total P and macroinvertebrate diversity exhibits a threshold. Diversity decreases as P increases up to a point, and then decreases less rapidly above a breakpoint (Evans-White et al. 2009; Fig. 3A). The proposed mechanism for this threshold is that consumers that specialize on low-P food are less competitive when P is abundant in the water column. In contrast, predators meet their P requirement by consuming relatively P-rich animal prey and are less directly affected by water-column P. The fact that predators do not demonstrate a strongly defined P threshold (Fig. 3B) but consumers do (Fig. 3A) provides support for the mechanism. Whether macroinvertebrate diversity can recover with P control and whether this alternative state is stable are not known. The implication for management is that P should be kept below the threshold to maintain diversity.

Representative Case Studies From This Issue

The papers in this BRIDGES cluster (Clements et al. 2010, Hilderbrand et al. 2010, King and Baker 2010) or associated with the cluster (Gido et al. 2010) describe cases of thresholds, some of which are characterized by alternative stable states.

An increase in impervious surfaces in watersheds can lead to abrupt changes in macroinvertebrate assemblages. Whether these changes represent an alternative stable state is not clear, but threshold data can be used to estimate effects of urbanization on regional macroinvertebrate biodiversity. Hilderbrand et al. (2010) described a series of species-specific thresholds at which extirpation occurs abruptly in response to increases in impervious cover, and they used these thresholds to predict the species of stream macroinvertebrates likely to be extirpated with increased urbanization. King and Baker (2010) used a newly developed technique to illustrate changes in entire communities across stress gradients. They used simulated data and data on impervious surfaces and macroinvertebrates as test cases to identify thresholds that were not apparent in analyses based on traditional community metrics.

Many species begin declining well before they have reached the point where they are destined for extinction or extirpation. The point at which a species begins to respond negatively to a stressor represents a subtle and difficult-to-identify threshold (King and Baker 2010). One way to detect early signs of decline and the point at which a species is effectively lost from the landscape is to compare cumulative frequency distributions of observed against expected distributions along gradients of potential stressors. Utz et al. (2009) used this technique to identify sensitivity of benthic macroinvertebrate taxa to landuse change and to test regional differences in sensitivity. This approach also can be used to forecast biodiversity loss in the face of changing landscapes (Hilderbrand et al. 2010). These tools for identifying thresholds early in a time series are useful to managers because they allow identification of species of concern in stressed landscapes.

Groundwater pumping and reservoir construction have shifted fish assemblages into alternative stable states. Streams in the Great Plains that rely on the Ogallala aquifer for base flow have experienced an abrupt change in the quantity and variability in stream flow since the 1960s when groundwater pumping rapidly increased. These changes coincided with construction of impoundments of various sizes and have strongly altered regional fish assemblages (Gido et al. 2010). These modifications abruptly altered the habitat of stream biota, but because stream networks are highly heterogeneous, many taxa maintained populations until recently (i.e., 10 y ago). Moreover, the distribution of invasive species in some areas expanded 10 to 20 y after reservoir construction. In this system, time-lagged responses to environmental stressors were observed at large spatial and temporal scales. The mechanisms underlying the changes are species-specific responses caused by the interaction of life-history traits with physical habitat changes caused by reservoir construction and drying of small streams by groundwater withdrawal. The altered state is not stable over geological timescales, but is stable relative to generation times of the fishes.

Recovery over time in disturbed streams also can display nonlinear patterns. Clements et al. (2010) described a statistical technique that can be used to assess recovery trajectories and identify thresholds occurring over time. They found multiple thresholds in macroinvertebrate communities following restoration of part of a river damaged by mining waste. Their study illustrated the complex nonlinear nature of recovery and that managers should not assume that simple recovery trajectories will result from mitigation techniques.

Conclusions on Thresholds, Stable States, and Management

Detection of thresholds in advance might be possible, but the field is in its infancy (Scheffer et al. 2009). We lack enough ecological information in most systems to make a priori mechanistic predictions of where thresholds will occur, but thresholds can be identified empirically. If a threshold exists, it should be assumed (under the precautionary principle) that return will be difficult once the threshold is crossed because predicting whether the system has moved to an alternative stable state is difficult (Bellwood et al. 2004). Management decisions that might cause a system to approach an ecological threshold should be viewed with caution because the alternative state could be costly in terms of economic damages, lost opportunities, and restoration efforts.


We thank the US Environmental Protection Agency Science to Achieve Results (STAR) program for financial support (grant R832446 grant to WKD and KBG; R832441 to WHC; R832444 to RHH). WKD thanks M. Evans-White for providing data, D. Gudder for editing the manuscript, P. Silver and A. Roy for suggestions on the manuscript, A. Roy for organizing this BRIDGES cluster, and members of the Department of Ecology at the University of Barcelona for helpful suggestions. This is publication 10-310-J from the Kansas Agricultural Experiment Station.

Literature Cited


T. Andersen, J. Carstensen, E. Hernández-García, and C. Duarte . 2009. Ecological thresholds and regime shifts: approaches to identification. Trends in Ecology and Evolution 24:49–57. Google Scholar


M. J. Anderson 2008. Animal-sediment relationships re-visited: characterising species' distributions along an environmental gradient using canonical analysis and quantile regression splines. Journal of Experimental Marine Biology and Ecology 366:16–27. Google Scholar


M. E. Baker and R. S. King . 2010. A new method for detecting and interpreting biodiversity and ecological community thresholds. Methods in Ecology and Evolution 1:25–37. doi: 10.1111/j.2041-210X.2009.00007. Google Scholar


D. R. Bellwood, T. P. Hughes, C. Folke, and M. Nystrom . 2004. Confronting the coral reef crisis. Nature 429:827–833. Google Scholar


L. Breiman, J. H. Friedman, R. A. Olshen, and C. J. Stone . 1984. Classification and regression trees. Wadsworth International Group. Belmont, California. Google Scholar


T. Brenden, L. Wang, and Z. Su . 2008. Quantitative identification of disturbance thresholds in support of aquatic resource management. Environmental Management 42:821–832. Google Scholar


B. S. Cade and B. R. Noon . 2003. A gentle introduction to quantile regression for ecologists. Frontiers in Ecology and the Environment 1:412–420. Google Scholar


S. Carpenter 2003. Regime shifts in lake ecosystems: pattern and variation. Ecology Institute. Oldendorf/Luhe, Germany. Google Scholar


S. R. Carpenter, W. A. Brock, J. J. Cole, J. F. Kitchell, and M. L. Pace . 2008. Leading indicators of trophic cascades. Ecology Letters 11:128–138. Google Scholar


S. R. Carpenter, D. Ludwig, and W. A. Brock . 1999. Management of eutrophication for lakes subject to potentially irreversible change. Ecological Applications 9:751–771. Google Scholar


P. Chaudhuri and W. Loh . 2002. Nonparametric estimation of conditional quantiles using quantile regression trees. Bernoulli 8:561–576. Google Scholar


W. H. Clements, N. K. M. Vieira, and D. L. Sonderegger . 2010. Use of ecological thresholds to assess recovery in lotic ecosystems. Journal of the North American Benthological Society 29:1017–1023. Google Scholar


G. De'ath 2002. Multivariate regression trees: a new technique for modeling species-environment relationships. Ecology 83:1105–1117. Google Scholar


G. De'ath and K. E. Fabricius . 2000. Classification and regression trees: a powerful yet simple technique for ecological data analysis. Ecology 81:3178–3192. Google Scholar


C. L. Dent, G. S. Cumming, and S. R. Carpenter . 2002. Multiple states in river and lake ecosystems. Philosophical Transactions of the Royal Society of London Series B: Biological Sciences 357:635–645. Google Scholar


W. K. Dodds 2008. Humanity's footprint: momentum, impact and our global environment. Columbia University Press. New York. Google Scholar


W. K. Dodds 2009. Laws, theories, and patterns in ecology. University of California Press. Berkeley, California. Google Scholar


W. K. Dodds, J. C. Priscu, and B. K. Ellis . 1991. Seasonal uptake and regeneration of inorganic nitrogen and phosphorus: size fractionation and antibiotic treatment. Journal of Plankton Research 13:1339–1358. Google Scholar


W. K. Dodds, V. H. Smith, and K. Lohman . 2002. Nitrogen and phosphorus relationships to benthic algal biomass in temperate streams. Canadian Journal of Fisheries and Aquatic Sciences 59:865–874. Google Scholar


M. A. Evans-White, W. K. Dodds, D. Huggins, and D. Baker . 2009. Thresholds in macroinvertebrate biodiversity and stoichiometry across water-quality gradients in Central Plains lotic systems. Journal of the North American Benthological Society 28:855–868. Google Scholar


W. Fagan, P. Unmack, C. Burgess, and W. Minckley . 2002. Rarity, fragmentation, and extinction risk in desert fishes. Ecology 83:3250–3256. Google Scholar


D. Fox 2007. Ecology – back to the no-analog future? Science 316:823. Google Scholar


G. Gal and W. Anderson . 2010. A novel approach to detecting a regime shift in a lake ecosystem. Methods in Ecology and Evolution 1:45–52. Google Scholar


J. E. Garvey, E. A. Marschall, and R. A. Wright . 1998. From star charts to stoneflies: detecting relationships in continuous bivariate data. Ecology 79:442–447. Google Scholar


K. B. Gido, W. K. Dodds, and M. E. Eberle . 2010. Retrospective analysis of fish community change during a half-century of landuse and streamflow changes. Journal of the North American Benthological Society 29:970–987. Google Scholar


P. Groffman, J. Baron, T. Blett, A. Gold, I. Goodman, L. Gunderson, B. Levinson, M. Palmer, H. Paerl, G. Peterson, N. Poff, D. Rejeski, J. Reynolds, M. Turner, K. Weathers, and J. Wiens . 2006. Ecological thresholds: the key to successful environmental management or an important concept with no practical application? Ecosystems 9:1–13. Google Scholar


L. Gunderson 2000. Ecological resilience in theory and application. Annual Review of Ecology and Systematics 31:425–439. Google Scholar


J. Halley 1996. Ecology, evolution and 1/f-noise. Trends in Ecology and Evolution 11:33–37. Google Scholar


J. S. Harding, E. F. Benfield, P. V. Bolstad, G. S. Helfman, and E. B. D. Jones . 1998. Stream biodiversity: the ghost of land use past. Proceedings of the National Academy of Sciences of the United States of America 95:14843–14847. Google Scholar


J. B. Heffernan 2008. Wetlands as an alternative stable state in desert streams. Ecology 89:1261–1271. Google Scholar


R. H. Hilderbrand, R. M. Utz, S. A. Stranko, and R. L. Raesly . 2010. Applying thresholds to forecast potential biodiversity loss from human development. Journal of the North American Benthological Society 29:1009–1016. Google Scholar


T. Hughes, D. Bellwood, C. Folke, R. Steneck, and J. Wilson . 2005. New paradigms for supporting the resilience of marine ecosystems. Trends in Ecology and Evolution 20:380–386. Google Scholar


H. Jelks, S. Walsh, N. Burkhead, S. Contreras-Balderas, E. Diaz-Pardo, D. Hendrickson, J. Lyons, N. Mandrak, F. McCormick, and J. Nelson . 2008. Conservation status of imperiled North American freshwater and diadromous fishes. Fisheries 33:372–386. Google Scholar


R. S. King and M. E. Baker . 2010. Considerations for analyzing ecological community thresholds in response to anthropogenic environmental gradients. Journal of the North American Benthological Society 29:998–1008. Google Scholar


R. S. King and C. J. Richardson . 2003. Integrating bioassessment and ecological risk assessment: an approach to developing numerical water-quality criteria. Environmental Management 31:795–809. Google Scholar


J. Martin, M. C. Runge, J. D. Nichols, B. C. Lubow, and W. L. Kendall . 2009. Structured decision making as a conceptual framework to identify thresholds for conservation and management. Ecological Applications 19:1079–1090. Google Scholar


R. M. May 1973. Stability and complexity in model ecosystems. Princeton University Press. Princeton, New Jersey. Google Scholar


R. M. May 1977. Thresholds and breakpoints in ecosystems with a multiplicity of stable states. Nature 269:471–477. Google Scholar


A. Mayer and M. Rietkerk . 2004. The dynamic regime concept for ecosystem management and restoration. BioScience 54:1013–1020. Google Scholar


P. C. D. Milly, J. Betancourt, M. Falkenmark, R. M. Hirsch, Z. W. Kundzewicz, D. P. Lettenmaier, and R. J. Stouffer . 2008. Stationarity is dead: whither water management? Science 319:573–574. Google Scholar


J. M. O'Brien and W. K. Dodds . 2010. Saturation of nitrate uptake in prairie streams as a function of acute and chronic nitrogen exposure. Journal of the North American Benthological Society 29:627–635. Google Scholar


J. M. O'Brien, W. K. Dodds, K. C. Wilson, J. N. Murdock, and J. Eichmiller . 2007. The saturation of N cycling in Central Plains streams: 15N experiments across a broad gradient of nitrate concentrations. Biogeochemistry 84:31–49. Google Scholar


J. F. Paul and M. E. McDonald . 2005. Development of empirical, geographically specific water quality criteria: a conditional probability analysis approach. Journal of the American Water Resources Association 41:1211–1223. Google Scholar


C. Pawlowski 2006. Dynamic landscapes, stability and ecological modeling. Acta Biotheoretica 54:43–53. Google Scholar


R. H. Peters 1991. A critique for ecology. Cambridge University Press. Cambridge, UK. Google Scholar


S. S. Qian, R. S. King, and C. J. Richardson . 2003. Two methods for the detection of environmental thresholds. Ecological Modeling 166:87–97. Google Scholar


C. T. Robinson and U. Uehlinger . 2008. Experimental floods cause ecosystem regime shift in a regulated river. Ecological Applications 18:511–526. Google Scholar


S. Rodionov 2004. A sequential algorithm for testing climate regime shifts. Geophysical Research Letters 31:L09204. Google Scholar


M. Scheffer, J. Bascompte, W. Brock, V. Brovkin, S. Carpenter, V. Dakos, H. Held, E. Nes, M. Rietkerk, and G. Sugihara . 2009. Early-warning signals for critical transitions. Nature 461:53–59. Google Scholar


M. Scheffer and S. R. Carpenter . 2003. Catastrophic regime shifts in ecosystems: linking theory to observation. Trends in Ecology and Evolution 18:648–656. Google Scholar


M. Scheffer, S. Carpenter, J. A. Foley, C. Folke, and B. Walker . 2001. Catastrophic shifts in ecosystems. Nature 413:591–596. Google Scholar


K. Slavik, B. J. Peterson, L. A. Deegan, W. B. Bowden, A. E. Hershey, and J. E. Hobbie . 2004. Long-term responses of the Kuparuk River ecosystem to phosphorus fertilization. Ecology 85:939–954. Google Scholar


D. L. Sonderegger, H. Wang, W. H. Clements, and B. R. Noon . 2009. Using SiZer to detect thresholds in ecological data. Frontiers in Ecology and the Environment 7:190–195. Google Scholar


R. Thom 1972. Stabilité structurelle et morphogénèse: essai d'une théorie générale des modèles. WA Benjamin. Reading, Massachusetts. Google Scholar


R. M. Utz, R. H. Hilderbrand, and D. M. Boward . 2009. Identifying regional differences in threshold responses of aquatic invertebrates to land cover gradients. Ecological Indicators 9:556–567. Google Scholar


J. W. Williams and S. T. Jackson . 2007. Novel climates, no-analog communities, and ecological surprises. Paleoecology 5:475–482. Google Scholar


P. J. L. Williams 1973. The validity of the application of simple kinetic analysis to heterogeneous microbial populations. Limnology and Oceanography 18:159–165. Google Scholar


J. T. Wootton 2010. Experimental species removal alters ecological dynamics in a natural ecosystem. Ecology 91:42–48. Google Scholar


[1] BRIDGES is a recurring feature of J-NABS intended to provide a forum for the interchange of ideas and information relevant to J-NABS readers, but beyond the usual scope of a scientific paper. Articles in this series may integrate science into ecosystem management or bridge aquatic ecology to other disciplines, e.g., political science, economics, education, chemistry, or other biological sciences. Papers may be complementary or take alternative viewpoints. Authors with ideas for topics should contact Associate Editors Ashley Moerke and Allison Roy.

Ashley Moerke,

Allison Roy,


Walter K. Dodds, William H. Clements, Keith Gido, Robert H. Hilderbrand, and Ryan S. King "Thresholds, breakpoints, and nonlinearity in freshwaters as related to management," Journal of the North American Benthological Society 29(3), 988-997, (29 September 2010).
Received: 19 October 2009; Accepted: 11 May 2010; Published: 29 September 2010

Back to Top