## Abstract

Dams impound the majority of rivers and provide important societal benefits, especially daily water releases that enable on-peak hydroelectricity generation. Such “hydropeaking” is common worldwide, but its downstream impacts remain unclear. We evaluated the response of aquatic insects, a cornerstone of river food webs, to hydropeaking using a life history–hydrodynamic model. Our model predicts that aquatic-insect abundance will depend on a basic life-history trait—adult egg-laying behavior—such that open-water layers will be unaffected by hydropeaking, whereas ecologically important and widespread river-edge layers, such as mayflies, will be extirpated. These predictions are supported by a more-than-2500-sample, citizen-science data set of aquatic insects from the Colorado River in the Grand Canyon and by a survey of insect diversity and hydropeaking intensity across dammed rivers of the Western United States. Our study reveals a hydropeaking-related life history bottleneck that precludes viable populations of many aquatic insects from inhabiting regulated rivers.

More than 800,000 dams exist worldwide (Richter and Thomas 2007), and the majority of Earth's rivers are dammed (Nilsson et al. 2005). Such flow management provides numerous societal benefits, including water storage, flood control, and hydropower production (World Commission on Dams 2000). The ecological upshot of all this damming is that rivers are some of the most extensively altered ecosystems on Earth (Carpenter et al. 2011), and flow regimes among large rivers are becoming homogenized as the timing and magnitude of impounded releases are engineered to meet societal needs (Poff et al. 2007). It is widely recognized that dams directly affect population viability for aquatic species by creating a barrier to movement and migration (Kareiva et al. 2000, Dugan et al. 2010). However, far less is known about the specific mechanisms underlying downstream ecological responses to hydrologic flow modification (Bunn and Arthington 2002, Poff and Zimmerman 2010).

Hydroelectricity production is a primary purpose of many dams, particularly the world's largest and most iconic, including the Three Gorges Dam on the Yangtze River in China, the Itaipu Dam on the Paraná River in Brazil and Paraguay, and the Hoover Dam on the Colorado River in the United States (World Commission on Dams 2000). Hydropower provides 19% of the world's electricity supply, far exceeding the generation of all other renewable sources combined (World Commission on Dams 2000, Zarfl et al. 2015). Governments around the world are also planning extensive new development of hydroelectricity potential in response to energy and climate crises (Kao et al. 2014, Zarfl et al. 2015), even though the damming of rivers has substantial environmental costs, including habitat loss, fishery collapse, and biological extinctions (Vörösmarty et al. 2010, Liermann et al. 2012). However, we contend that a key dimension of these environmental costs—and a mechanism underpinning many others—has been overlooked, contributing to an incomplete assessment of environmental trade-offs. As we demonstrate, this cost arises from a hitherto-unrecognized life-history bottleneck that flow management for hydropower production imposes on aquatic insects, ubiquitous organisms that play an essential role in food webs in and along the world's rivers.

Water releases from hydropower dams often vary at hourly timescales in a practice known as load following or hydropeaking (hereafter hydropeaking), whereby river flows are increased during the day when energy demand is high and decreased at night when demand is low (Førsund 2015). Hourly changes in discharge associated with hydropeaking can be substantial, with discharge varying by a factor of 10 or more within a day (Moog 1993, Topping et al. 2003). These large hourly changes in discharge produce kinematic waves that can propagate downstream for distances of more than 400 kilometers (km; Wiele and Smith 1996), creating an extensive intertidal zone along river shorelines that is absent from natural rivers and to which freshwater organisms are not adapted (Ward and Stanford 1979, Moog 1993). However, large dams impose multiple stressors on rivers, including altered flow, temperature, and sediment regimes (Poff et al. 2007, Schmidt and Wilcock 2008, Olden and Naiman 2010), and prior studies have struggled to disentangle the effects of hydropeaking from these other stressors (Arthington et al. 2006, Poff and Zimmerman 2010).

Hydropeaking and the artificial intertidal zone it creates have the potential to adversely affect numerous aquatic organisms, but strong deleterious impacts are particularly likely for organisms that rely on nearshore environments during one or more life stages. We selected aquatic insects for our investigation of hydropeaking impacts, because they are ubiquitous in freshwaters and represent the primary prey for myriad species of fish, birds, bats, and other wildlife living in and along rivers (Nakano and Murakami 2001, Baxter et al. 2005). These insect groups—especially mayflies, stoneflies, and caddisflies in the orders Ephemeroptera, Plecoptera, and Trichoptera (hereafter EPT)—are also widely used as bioindicators for rivers and are integral to freshwater regulatory policies in the United States, the European Union, and elsewhere (Fremling 1964, Lenat 1988, Carlisle et al. 2013).

Most aquatic insects have complex life cycles, with a winged adult life stage that is terrestrial whereas the egg, larval, and pupal stages are aquatic. Nonetheless, the vast majority of investigations into aquatic insects have focused on the larval life stages in isolation, whereas other life stages are traditionally ignored. However, this approach is currently undergoing a transformation, because the conditions necessary to support aquatic insects throughout their life cycles (egg, larva, pupa, and adult) are increasingly recognized as crucial to species persistence (Encalada and Peckarsky 2012, Muehlbauer et al. 2014).

The influence of recruitment (i.e., the number of eggs that develop into larvae) on population dynamics is poorly studied, particularly in the case of insects. Investigations into factors limiting the diversity or abundance of aquatic-insect assemblages have traditionally focused on studying larval life stages exclusively, because it was thought that the environmental conditions and biological interactions experienced by larvae (i.e., predation and competition) would invariably be the primary determinants of larval abundance. Aquatic insects spend a disproportionate amount of their lives in the larval stage, and adult females can lay hundreds to thousands of eggs, so it seemed unlikely that larval abundance would ever be limited by egg abundance or the environmental conditions experienced by nonlarval stages per se. However, several recent studies have called this assumption into question and demonstrate that the abundance of larvae can be strongly influenced by the quality and availability of egg-laying substrates at the start of the cohort (Encalada and Peckarsky 2012, Lancaster and Downes 2014, Macqueen and Downes 2015). In one compelling study, investigators experimentally varied the number of Baetis mayfly eggs present in stream reaches by simply manipulating the number of emergent rocks that were present in different pristine streams (Encalada and Peckarsky 2012). Adult Baetis females land on these rocks in fast water and then crawl under the rock to cement their eggs to the underside. Nearly a year after the emergent rocks were manipulated, the abundance of late-stage mayfly larvae had doubled in reaches where emergent rocks were added and declined by more than half in reaches where they had been eliminated. Therefore, recruitment dynamics—and the availability or quality of egg-laying substrates specifically—can be a primary determinant of aquatic-insect abundance in streams and rivers.

When viewed through this lens of egg laying and rearing, it becomes apparent that aquatic-insect populations below hydropeaking dams could be especially vulnerable to recruitment limitation. Over the course of a single day, these rivers are subject to large changes in river depth, which may dramatically affect the availability and quality of egg-laying substrates used by aquatic insects. For taxa such as Baetis that cement eggs to substrates, for example, a partially submerged rock that is wetted during high water at the time of egg laying could subsequently be exposed to air a few hours later during low water, potentially killing the eggs. Scaling up, acute egg mortality caused by hydropeaking could be capable of regulating aquatic-insect abundance throughout river segments via recruitment limitation and reducing biodiversity by extirpating aquatic insects with river-edge egg-laying behaviors, with attendant consequences for populations of insectivorous wildlife (Nakano and Murakami 2001, Baxter et al. 2005).

Encapsulating all of these insights, assumptions, and inferences, we propose the following novel hypothesis concerning the intersection of hydropeaking and aquatic-insect life history: Hydropeaking limits the recruitment of aquatic insects via acute egg mortality, constraining the abundance and diversity of aquatic-insect populations downstream of hydropeaking dams.

In the remainder of this article, we use multiple lines of evidence to test this novel hypothesis. We first formally test the two key assumptions implicit in this hypothesis: that most insects lay eggs in habitats vulnerable to drying by hydropeaking-induced water-level fluctuations and that drying reduces egg viability. Next, we develop a life history–hydrodynamic model that provides a predictive framework for exploring how different insect groups respond to hydropeaking, contingent on their specific egg-laying strategies. We then test predictions from this model using a large citizen-science data set of emergent insects collected throughout the 400-km-long Grand Canyon segment of the Colorado River. Finally, to investigate the consistency of hydropeaking effects on aquatic-insect assemblages, we compare insect diversity across 16 dammed rivers in the Western United States that span a range of hydropeaking intensity.

## Where do aquatic insects lay their eggs?

One major assumption that is implicit in our recruitment-limitation hypothesis is that many aquatic insects lay eggs along river shorelines. We tested this assumption by drawing on a recent synthesis of biological trait databases (Statzner and Beche 2010). The use of biological traits as indicators has gained momentum as a powerful approach for disentangling the effects of multiple stressors in aquatic ecosystems (Poff et al. 2006), and the development of comprehensive databases of biological traits for aquatic invertebrates is making this approach feasible on a continental scale (e.g., Vieira et al. 2006). For the purposes of evaluating egg-laying traits of aquatic insects, Statzner and Beche (2010) included descriptions for invertebrate genera spanning 96 North American taxa and 78 European taxa.

These insect trait databases provide strong evidence that the majority of aquatic insects exhibit egg-laying behaviors that will be vulnerable to hydropeaking (figure 1). Specifically, more than three-quarters of aquatic insects exhibit the type of cementing behavior shown by females of Baetis that were studied in the Encalada and Peckarsky (2012) experiment described earlier. Significantly, this behavior generally requires the presence of substrates that are partially emerged out of the water surface on which females can alight before crawling under water or, alternatively, substrates that are in shallow water that females can swim to for the purposes of attaching their eggs. Both of these classes of substrates are vulnerable to hydropeaking-related flow variation, because partially submerged rocks and shallow habitats at high water can become fully exposed to air and dry out when the water is low. Although some taxa do exhibit egg-laying behaviors that will be unaffected by an artificial intertidal zone—such as species that give birth to live young (ovoviviparous) or broadcast eggs on the water surface—analysis of these traits databases indicates that such strategies are uncommon among aquatic insects (figure 1). Therefore, we conclude that this implicit assumption of our hypothesis is valid and well founded: The majority of insects lay eggs in habitats that are susceptible to drying via daily hydropeaking water-level fluctuations.

Figure 1.

Aquatic insects often cement eggs to substrates along river margins. Represented here are the egg-laying strategies for the most common aquatic invertebrate genera in North America and Europe, representing 96 and 78 taxa, respectively. The error bars represent the standard error of the mean. Adapted with permission from Statzner and Beche 2010.

Figure 1.

Aquatic insects often cement eggs to substrates along river margins. Represented here are the egg-laying strategies for the most common aquatic invertebrate genera in North America and Europe, representing 96 and 78 taxa, respectively. The error bars represent the standard error of the mean. Adapted with permission from Statzner and Beche 2010.

## Does desiccation reduce egg viability?

In order for hydropeaking to limit aquatic-insect populations via acute egg mortality, desiccation on hydropeaking-relevant timescales must actually kill eggs. We directly tested this assumption by quantifying the viability of eggs that were exposed to brief periods of desiccation that are typical for hydropeaking rivers. Experiments were conducted using the eggs of a widespread genus of mayfly, Baetis (Baetidae), and two common, large river caddisfly genera, Brachycentrus (Brachycentridae) and Hydropsyche (Hydropsychidae). The experiments were conducted using insect eggs collected from the Green River downstream of the Flaming Gorge Dam, Utah, in June (caddisflies) and October (mayflies) of 2015. For caddisflies, egg masses attached to rocks were collected from nearshore habitats and assigned to one of four desiccation treatments: 0 (control), 4, 8, or 12 hours of streamside desiccation (n = 12–20, depending on the experiment and treatment level). Following the completion of each treatment, caddisfly egg masses were scraped from rocks, placed in individual vials, and stored in river water on ice. The treatments were initially conducted during both the day and the night, on the basis of the presumption that hotter air temperatures during the day would result in more rapid desiccation and egg mortality. However, both the day and night desiccation trials experienced extremely high mortality, and the ANOVA tests indicated that there was not a significant difference between day and night treatments (F-statistics = 0.001 and 0.042, and p-values = 0.978 and 0.837 for Brachycentrus and Hydropsyche, respectively). Therefore, the day and night treatments were combined for the remainder of the analysis, and the subsequent experiments on Baetis were conducted during the day only. The mayfly study also was conducted using eggs laid on slate tiles that had been placed throughout the stream rather than by scraping eggs off rocks, because low egg viability in the control groups for the caddisfly experiments indicated that scraping likely induced extraneous mortality. In addition, we added shorter duration treatments of one-half, 1, and 2 hours in the mayfly study to better identify critical desiccation exposure levels and conducted desiccation treatments in a laboratory setting instead of streamside. For both the caddisfly and mayfly experiments, the egg masses were reared at room temperature (23 degrees Celsius) on a 12-hour day–night light cycle for 5 weeks or until egg masses were no longer viable based on visual inspection. Egg viability was computed as the ratio of hatched eggs to the total number of eggs per egg mass.

These experiments provide convincing evidence that this assumption is also valid and well founded: Even brief desiccation markedly reduced egg viability (figure 2, ANOVA F-statistics = 21.500, 10.332, and 13.403 for Baetis, Brachycentrus, and Hydropsyche, respectively, and p-statistics < 0.001 for all). We did find that a half-hour of desiccation did not significantly reduce the viability of mayfly egg masses relative to undesiccated, control egg masses (t-statistic = 1.326, p-statistic = 0.099). However, after 1 hour or longer of desiccation, egg viability was significantly reduced for all three taxa compared with the control treatments, based on post hoc Tukey's tests. In fact, egg viability in all of these desiccation treatments of 1 hour or longer did not differ significantly from 0 (i.e., total egg mortality), and no eggs hatched from 136 out of 164 (83%) of these treatments. It is worth noting that these treatments represent desiccation exposure for a single day along a hydropeaking river. Because many aquatic-insect eggs take days to weeks to hatch, they are in fact exposed to several cycles of inundation and drying prior to hatching. Therefore, our desiccation experiments should be viewed as conservative; field egg mortality after several such cycles is likely even higher than suggested by our laboratory rearing results. Conducting additional experiments on different aquatic-insect taxa (e.g., Plecoptera, stoneflies, or certain Diptera, true flies) would naturally be insightful and add nuance to the patterns we report here. However, our experiments included three globally common genera spanning two ecologically important aquatic-insect orders, and our results were unequivocal to the extent that they are likely to be broadly representative of other taxa. We therefore conclude that aquatic-insect eggs that are laid in the artificial intertidal zone created by daily hydropeaking will be subject to acute mortality later in the same day, when river stage is lower.

Figure 2.

Desiccation causes high mortality of aquatic-insect eggs. Mean egg viability (number of hatched eggs/total eggs) after desiccation for (a) Baetis, (b) Brachycentrus, and (c) Hydropsyche egg masses. The points represent the mean viability of egg masses across 12–20 replicate experiments, depending on the treatment and taxon in question (see the main text for details). The error bars represent the standard error of the mean.

Figure 2.

Desiccation causes high mortality of aquatic-insect eggs. Mean egg viability (number of hatched eggs/total eggs) after desiccation for (a) Baetis, (b) Brachycentrus, and (c) Hydropsyche egg masses. The points represent the mean viability of egg masses across 12–20 replicate experiments, depending on the treatment and taxon in question (see the main text for details). The error bars represent the standard error of the mean.

## A life-history bottleneck arising from hydropeaking

Building on these egg-laying and desiccation results, we next developed a deterministic model to explore the interplay of hydropeaking waves with egg-laying strategies. Specifically, our model provides a predictive framework for understanding how these variables interact to affect aquatic-insect populations along a hydropeaking river continuum. Lateral (shoreline) inundation due to hydropeaking can be approximated as a sine wave with magnitude h at distance x downstream from a dam as follows:

(1)
$$h(x) = \frac{{({h_{\max }} + {h_{{\min}\, \small {\square}}})}}{2} + \frac{{({h_{\max }} - {h_{{\min}\, \small{\square}})}}}{2}*\cos (f*x)$$
where f determines the frequency of the wave, hmax is the maximum extent of lateral inundation, and hmin is the minimum extent of lateral inundation. As the sine wave propagates downstream, h(x) describes the degree of hydropeaking inundation that occurs on a given river segment at dusk, when most insect taxa are assumed to be laying their eggs (Pinder 1995, Merritt et al. 2008). Therefore, h(x) is an index of how severely hydropeaking affects recently deposited eggs at any location along the river. At locations with high values of h, eggs are laid when the river reach is at its daily high-flow peak, and deposited eggs will therefore be vulnerable to desiccation-induced mortality at low flow later that day and at the same time on each subsequent day. In contrast, when h(x) = 0, the river is at low flow during the time of egg laying, so newly deposited eggs will never be subjected to any flows lower than those present during egg laying, and these eggs will never be subject to desiccation.

We assumed a trade-off between per-egg survival (s) and egg-laying location relative to the river edge (0 ≤ r ≤ 1), such that eggs cemented to substrates along river edges experience the highest relative survival in the absence of hydropeaking:

(2)
$$s(r) = {e^{ - r*c}}$$
where c controls the steepness of the relationship. Such a trade-off occurs if shallow edge habitats provide more favorable rearing conditions for eggs (e.g., slower water that will allow river-edge specialists to cement eggs directly on suitable substrates) relative to midchannel habitats (e.g., only open-water generalists that dip eggs directly into the water are able to use these habitats for egg laying, and many of these eggs may settle on unsuitable substrates). Note that r is measured relative to the river edge (i.e., the river edge occurs at r = 0 and river center at r = 1), and this will change in response to hydropeaking. Therefore, exclusive of any hydropeaking effects, maximum total egg survival, wmax, in a river reach is given by the area under equation 2 bounded by the portion of the river cross-section used for egg laying (r1 to r2), which is a species-specific quantity:
(3)
$${w_{\max }} = \int_{{r_1}}^{{r_2}} {{e^{ - r*c}}d{r_{\max }}}$$

Although any egg-laying strategy is possible, we consider the case where each insect species uses a characteristic portion of the river with respect to the river's edge, and for simplicity, we treat the width of this proportion (r2r1) as constant. For example, river-edge specialists might lay eggs uniformly over the interval [0, 0.2] very near the shoreline, whereas open-water generalists might lay eggs uniformly in the thalweg [0.8, 1]. Under equation 3, the eggs of river-edge specialists will always have the highest potential survival (wmax) relative to other egg-laying strategies, but hydropeaking may strand some or all of the eggs deposited at a particular location such that the realized survival (w) is lower than wmax. The survival of eggs deposited within the zone affected by hydropeaking will be reduced by whydro, the portion of the egg-laying zone that is lost to desiccation:

(4)
$$w = {w_{\max }} - {w_{{\rm{hydro}}}}$$

(5)
$${\rm{if}}\,{r_1} < h(k) < {r_2},\,{w_{{\rm{hydro}}}} = \int_{{r_1}}^{h(k)} {{e^{ - rc}}dr}$$

(6)
$${\rm{if}}\,h(k) < {r_1},\,{w_{{\rm{hydro}}}} = \int_{{r_2}}^{{r_1}} {{e^{ - rc}}dr = 0}$$

(7)
$${\rm{if}}\,h(k) < {r_2},\,{w_{{\rm{hydro}}}} = \int_{{r_1}}^{{r_2}} {{e^{ - rc}}dr = {w_{\max }}}$$
In equation 5, only part of the egg-laying zone is lost because of hydropeaking, with concomitant effects for population level egg survival. In contrast, equations 6 and 7 describe scenarios in which none or all of the egg-laying zone, respectively, is lost.

Our life history–hydrodynamic model predicts that desiccation-induced egg mortality will extirpate river-edge egg layers from hydropeaking rivers (figure 3), particularly mayflies and other EPT taxa that cement eggs to substrates at the river margin or other zones subject to exposure under daily low hydropeaking flows (Statzner and Beche 2010, Encalada and Peckarsky 2012). In contrast, open-water egg layers, such as some blackfly species (e.g., Simulium arcticum; Adler et al. 2004), will be minimally affected by hydropeaking (figure 3). These divergent egg-laying strategies represent an example of a classic life-history trade-off that may even provide a basis for why EPT taxa are useful as bioindicators in the first place: Eggs laid by such river-edge specialists are likely to experience high survival when conditions remain ideal but are susceptible to complete mortality from environmental perturbations that cause conditions to suddenly change (e.g., shoreline desiccation). On the other end of the spectrum, eggs broadcast on the water surface by open-water generalists are likely to always experience relatively high mortality because many eggs will settle on unsuitable substrates; nonetheless, some eggs will just as invariably settle on ideal substrates. Finally, some taxa, such as midges (Chironomidae), exhibit an intermediate strategy. Taken as a group, midges lay their eggs generically along shorelines in a fashion that is neither strictly dependent on emergent rocks and vegetation nor broadcasting over open water (Pinder 1995). Specifically, most adult female midges tend to cement eggs to substrates, but some broadcast eggs freely (Williams 1982, Pinder 1995). Furthermore, when eggs are cemented, midge behavior differs from that of EPT taxa such as Baetis in that midges land at or on the water surface to release their eggs from their abdomen and do not actually crawl under water (Branch 1928, Pinder 1995). During this time between egg laying and cementing, many eggs are lost to open water; indeed, egg drift due to this behavior is substantial and has been estimated at 4000 eggs per hour per square meter through a river cross-section (Williams 1982). For intermediate strategists such as these midges, the model predicts a spatial periodicity in abundance that correlates with the timing of daily hydropeaking waves. Specifically, population abundance should be greatest in river reaches where the lowest daily flow occurs coincident with the peak timing of egg laying, because eggs laid in these locations will remain wetted and will never be subject to desiccation, but these insects should also be found at low abundance throughout the river.

Figure 3.

A life history–hydrodynamic model. Output from a life history–hydrodynamic model parameterized for the Colorado River in the Grand Canyon shows that as hydropeaking waves propagate downstream, the locations where daily flow minima occur at dusk are consistently located around river kilometer (km) 100 and 275. River-edge egg layers, such as mayflies (red line), are eliminated from hydropeaking rivers because of desiccation and the mortality of eggs. Open-water egg layers, such as Simulium arcticum (blackflies; green line) occur at all points along hydropeaking rivers. Intermediate strategists, such as midges (yellow line), exhibit spatial periodicity in abundance, with the highest abundance at locations where the timing of insect egg laying, generally at dusk, is in phase with daily flow minima. This figure illustrates equation 7, assuming r2 – r1 = 0.2, c = 2, and f = 0.033 (see the main text for details).

Figure 3.

A life history–hydrodynamic model. Output from a life history–hydrodynamic model parameterized for the Colorado River in the Grand Canyon shows that as hydropeaking waves propagate downstream, the locations where daily flow minima occur at dusk are consistently located around river kilometer (km) 100 and 275. River-edge egg layers, such as mayflies (red line), are eliminated from hydropeaking rivers because of desiccation and the mortality of eggs. Open-water egg layers, such as Simulium arcticum (blackflies; green line) occur at all points along hydropeaking rivers. Intermediate strategists, such as midges (yellow line), exhibit spatial periodicity in abundance, with the highest abundance at locations where the timing of insect egg laying, generally at dusk, is in phase with daily flow minima. This figure illustrates equation 7, assuming r2 – r1 = 0.2, c = 2, and f = 0.033 (see the main text for details).

## Insect abundance and diversity along a hydropeaking river continuum

We parameterized our life history–hydrodynamic model for the specific conditions present along the Colorado River downstream from the Glen Canyon Dam in the Grand Canyon, United States. Because of its canyon-bound setting and the absence of large tributaries, the daily hydropeaking wave released from the Glen Canyon Dam propagates far downstream, with hourly changes of 1 meter in river stage still present more than 400 km downstream, where the Colorado River enters its next reservoir, Lake Mead (Wiele and Smith 1996). This makes the Colorado River in the Grand Canyon an ideal case study because there is a wide range of variation in the degree of synchrony between the timing of egg laying (i.e., dusk) and the timing of minimum flows. Sampling along this remote segment of the Colorado River nonetheless presents logistical challenges, because most reaches are only accessible by two-week-long rafting trips. Therefore, to quantify aquatic-insect abundance throughout the Grand Canyon, we collaborated with river rafters to sample the adult life stage of aquatic insects, the abundance of which is directly related to larval abundance (Statzner and Resh 1993). Each evening in camp, these citizen scientists deployed fluorescent light traps for 1 hour near the river's edge, ultimately collecting more than 2500 samples (see box 1, figure 4, and Acknowledgments).

Box 1. Little bugs, big data, and the Grand Canyon: The role of citizen science in Colorado River adaptive management.

The closure of the Glen Canyon Dam in 1963 fundamentally altered the physical template of the 400-kilometer-long segment of the Colorado River in the Glen, Marble, and Grand Canyons (Schmidt et al. 1998). For instance, water clarity is considerably higher because Lake Powell reservoir traps millions of tons of sediment and organic matter annually (Topping et al. 2000), hypolimnetic releases lead to relatively cold and constant water temperatures (Voichick and Wright 2007), and flow management dampens the annual low and high flow periods, whereas hydropeaking greatly increases hourly flow variation (Topping et al. 2003). These changes in the physical template, along with accidental and intentional introductions of organisms (Blinn and Cole 1991), have completely restructured aquatic food webs (Cross et al. 2013) and led to declines and local extirpations of native, endangered fish populations (Minckley 1991). Ongoing adaptive management of the Glen Canyon Dam releases seeks to rehabilitate the Grand Canyon ecosystem and benefit key resources, including native and desired nonnative fish populations (www.gcdamp.gov).

Science plays an essential role in the adaptive management of the Glen Canyon Dam, but it has proven challenging for professional scientists to collect the type of high-resolution data needed to inform the management of this highly altered and remote ecosystem. Specifically, most reaches of the Colorado River are only accessible by two-week-long river trips that travel the entire 400-kilometer-long segment, which greatly limits the spatial and temporal extent of sampling regimens. However, starting in the early 2000s, physical scientists began using automated sensors to continuously monitor suspended sediment concentration and, for the first time, demonstrated a clear link between hydropeaking operations, sediment transport, and the erosion of beaches in the Grand Canyon (Topping et al. 2004, Wright et al. 2008). More recently, the continuous measurement of ecosystem metabolism using dissolved oxygen monitors revealed that hydropeaking operations have a significant, albeit minor, effect on algae production in the Grand Canyon (Hall et al. 2015). Any similar solutions to the continuous monitoring of animal populations using sensors have proven elusive, however, so river trips staffed by professional scientists have remained the primary tool for investigations into animal population dynamics. However, testing predictions of our life history–hydrodynamic model using traditional benthic surveys of larval insects would have required dozens of such river trips through the Grand Canyon at a cost of millions of dollars.

## Ecosystem consequences of biodiversity loss  and a path forward

Although some may argue about the extent to which aquatic insects have value or importance in their own right, in practical terms, unhealthy aquatic invertebrate assemblages do have tangible negative impacts on wildlife populations that are universally valued by society (figure 8). For instance, recent food-web and bioenergetics studies demonstrate that in the popular Lees Ferry sport fishery downstream of the Glen Canyon Dam, the maximum size and growth of rainbow trout are limited by the abundance and overall small size of their invertebrate prey (Cross et al. 2011, Dodrill et al. 2016). In addition, the simple food-web architecture in Lees Ferry results in rainbow trout populations that are inherently unstable and not resistant to controlled flood experiments that are released from the Dam (Cross et al. 2013). Farther downstream in the Grand Canyon, food-web studies indicate that the abundance and distribution of native fishes, including endangered humpback chub (Gila cypha), are also limited by the availability of insect prey; native fish populations consume virtually all of the available annual midge and blackfly production (Cross et al. 2013).

Figure 8.

Aquatic insects play an essential role in river and riparian food webs. Aquatic insects are ubiquitous in freshwaters and are the primary prey for myriad species of wildlife living in and along rivers. These insects have complex life cycles that include a terrestrial winged adult life stage, whereas egg, larval, and pupal stages are aquatic. Ecologically important insect groups such as mayflies, stoneflies, and caddisflies cement their eggs along river-edge habitats, making them especially sensitive to dam water management practices such as hydropeaking that affect these edge habitats.

Figure 8.

Aquatic insects play an essential role in river and riparian food webs. Aquatic insects are ubiquitous in freshwaters and are the primary prey for myriad species of wildlife living in and along rivers. These insects have complex life cycles that include a terrestrial winged adult life stage, whereas egg, larval, and pupal stages are aquatic. Ecologically important insect groups such as mayflies, stoneflies, and caddisflies cement their eggs along river-edge habitats, making them especially sensitive to dam water management practices such as hydropeaking that affect these edge habitats.

River managers are increasingly conducting environmental-flow experiments that mimic key aspects of natural flow regimes to rehabilitate river ecosystems or achieve specific ecological outcomes (Acreman et al. 2014, Olden et al. 2014). Incorporating knowledge of life stage–specific requirements for fish is an axiomatic component of such environmental flows. For instance, controlled floods are released from many dams to clean gravels of fine sediment and improve spawning habitat for salmonids (Olden et al. 2014). Similarly, river managers are designing environmental flows that enhance the flow conditions experienced by insect larvae. However, because the importance of recruitment dynamics to insect populations has only recently been demonstrated (Encalada and Peckarsky 2012, Lancaster and Downes 2014, Macqueen and Downes 2015), the flow conditions necessary to sustain other life stages have not yet been considered. Furthermore, implementing environmental flows is challenging in highly managed rivers because of the juxtaposition of uncertain environmental benefits against the readily quantified economic losses associated with reduced hydroelectricity generation (Jacobson and Galat 2008).

Our study informs the design of cost-effective environmental flows that should enhance biodiversity and ecosystem function downstream of hydropower dams on the Colorado River and elsewhere. Specifically, our study suggests that reducing hourly discharge variation during periods of peak aquatic-insect egg laying should alleviate the life-history bottleneck that arises from hydropeaking operations. Aquatic insects can be extremely fecund, with a single female laying hundreds to thousands of eggs (Merritt et al. 2008, Statzner and Beche 2010). Therefore, alleviating the life-history bottleneck that hydropeaking imposes on aquatic insects may not require long blocks of stable flow releases that completely preclude hydropeaking. For example, hydropeaking is less lucrative on weekends when electricity demands are low (Førsund 2015), so a cost-effective environmental flow could involve releasing stable and low flows every weekend during periods of peak aquatic-insect egg laying. Releasing low flows every weekend would ensure that eggs laid on weekends remained wetted and were never subject to desiccation prior to hatching, which typically occurs after days to weeks of incubation (Merritt et al. 2008, Statzner and Beche 2010). This type of environmental flow would minimally affect hydroelectricity revenues (USBR 2016) while substantially improving the quality of substrates available for aquatic-insect egg laying and rearing. Environmental flows such as this may allow highly managed river ecosystems to continue meeting societal needs for renewable hydroelectricity while ensuring the sustainable provisioning of critical ecosystem services that are provided by the world's rivers.

This article is dedicated to the professional river guides, private boaters, and organizations that participated in or facilitated the citizen-science light trapping project: Arizona Raft Adventures, Arizona River Runners, Arizona Game and Fish Department, Eric Baade, Matt Bryan, Riley Burch, Kirk Burnett, Canyon Expeditions, Canyon REO, Canyoneers, David Cassidy, Ceiba Adventures, Laura Chamberlain, Colorado River and Trail Expeditions, Jerry Cox, Bob Dye, Grand Canyon Expeditions, Grand Canyon National Park, Grand Canyon River Guides, Grand Canyon Youth, Amy Harmon, Hatch River Expeditions, Scott Jernigan, Ethan Johnson, Walker Mackay, Kelly McGrath, Moenkopi Riverworks, Ariel Neill, Outdoors Unlimited, Marc Perkins, Wade Permar, Katie Proctor, Professional River Outfitters, Matt Robinson, Orea Roussis, Gibney Siemion, Connie Tibbitts, John Toner, Jamie Townsend, Tour West, Kelly Wagner, Wilderness River Adventures, Kelly Williams, Kelsey Wogan, Kiki Wykstra, and Glade Zarn. We thank Lynn Hamilton of Grand Canyon River Guides and Emma Wharton of Grand Canyon Youth for their ongoing support and engagement. We thank Daren Carlisle (US Geological Survey), Mark Nelson (Bureau of Reclamation), Raymond Perkins (Oregon Department of Fish and Wildlife), Andrew Welch (PPL Montana), and Marc Wethington (New Mexico Department of Game and Fish) for providing invertebrate data used in the regional analysis. Jeremy Monroe of Freshwaters Illustrated developed the conceptual model (figure 8). We thank Matt Schroer and Jesse Fleri for conducting the egg desiccation experiments. TAK thanks Jack Schmidt for the opportunity to participate in the 2011 Lodore Canyon river trip that inspired this project. Funding for this study was provided by the Bureau of Reclamation's Glen Canyon Dam Adaptive Management Program, the US Geological Survey's Southwest Biological Science Center, and the Department of Energy's Western Area Power Administration. Finally, we are grateful for comments from Shahid Naeem, Sarah Hobbie, Jacques Finlay, Jane Lubchenco, Daren Carlisle, Brendan McKie, and Jack Schmidt on earlier drafts that greatly improved this manuscript. Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the US government.

## Supplemental material

The supplemental material is available online at http://bioscience.oxfordjournals.org/lookup/suppl/doi:10.1093/biosci/biw059/-/DC1. Data associated with this article are available at http://dx.doi.org/10.5066/F7WM1BH4.

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