Increased juvenile native fish abundance following a major flood in an Arizona river

Abstract Spring floods trigger spawning in many native fishes of the desert Southwest (USA), but less is known about fish community response when native fishes are rare. Here, we document change to native and nonnative fish captures and instream habitat features following a decade-high flooding event (2019) in the Verde River (AZ) where native fish captures were rare in the years pre-flood. Using prepositioned areal electrofishing devices (PAEDs), we sampled the fish community at 90 sampling units pre-flood (2017) and resampled those same units post-flood (2019) to compare and identify changes to catch and habitat features. Relative abundance of native fishes increased from 0.6% pre-flood (0.01 fish/PAED) to 53.0% post-flood (1.66 fish/PAED) and was largely attributable to the presence of juvenile Roundtail Chub Gila robusta (≤ 70 mm total length (TL)) and juvenile Sonora Sucker Catostomus insignis (≤ 100 mm TL). Juvenile Desert Sucker Catostomus clarkii experienced a lesser increase. One adult native fish was captured in 2017 and adult native fishes were absent from 2019 sampling. The catch of adult/subadult Common Carp Cyprinus carpio (> 100 mm TL) declined; however, this could be related to reservoir management and not the flood. The abundance of all size-classes of Black Bass Micropterus spp., Red Shiner Cyprinella lutrensis and other nonnative fishes did not change. The majority (97%) of juvenile native fishes were captured at the uppermost sampling reach. A 54% reduction to canopy cover across all sampling reaches and an increase of fine sediments at the most downstream reach demonstrates how floods can restructure the river environment. This case-study adds evidence that protection of spring floods is vital to the persistence and recolonization of fishes native to the desert Southwest, especially where they are rare. The continued presence of nonnative species may preclude juvenile native fishes from recruiting to adults.

Freshwater fishes native to the desert Southwest region of the United States are one of the most threatened faunal groups in North America (Rahel 2000). Of the 31 fish species native to the desert Southwest, 25 (> 80%) have experienced a significant decline or have been extirpated, and < 50% of the region's overall fish population is composed of native fishes (Olden and Poff 2005;Schade and Bonar 2005;Turner and List 2007). Understanding the factors associated with the abundance and distribution of native and nonnative fishes serves to benefit species conservation efforts.
In general, reproduction by native fishes of the desert Southwest is driven by river discharge and annual spring freshets. A positive relationship exists between spring floods, native fish spawning activity, and juvenile recruitment (Stefferud et al. 2011). High-magnitude spring floods trigger reproduction in Roundtail Chub Gila robusta, Sonora Sucker Catostomus insignis, and Desert Sucker Catostomus clarkii, among others (Brouder 2001;. It is thought that change to the instream environment (Propst and Gido 2004), the high magnitude flows (Bestgen et al. 2011), a temperature change associated with floods (Fraser et al. 2019), or some combination of these factors motivates this response.
Rapid onset floods, characteristic of rivers of the desert Southwest, may select against nonnative fishes (Minckley and Meffe 1987;Eby et al. 2003). Nonnative fishes of this region, with origins from mesic rivers of the southeastern United States, are often evolutionarily unfit to withstand these torrents. Therefore, a reduction to the abundance of nonnative fishes has been observed in rivers of the desert Southwest immediately following major floods (Minckley and Meffe 1987;Eby et al. 2003;Rogosch et al. 2019). Because of this, rapid onset floods have been credited with some rivers' ability to resist invasion by nonnative species. Nevertheless, some studies have observed the reduction of nonnative fishes to be transient and the nonnative fish community has returned to preflood levels rapidly (Pool and Olden 2015).
The importance of floods have been established for many native fishes of the desert Southwest (Brouder 2001;Propst et al. 2008); however, less is known about the potential for recolonization of a stream when the pre-flood abundance of native fishes is exceptionally low. Understanding the response by imperiled fish populations to large floods is becoming increasingly more important as native fish populations continue to decline Rogosch et al. 2019) and, increasingly, users are litigating for the rights to harvest flood waters (In re Aravaipa Canyon Wilderness Area, Contested Case No. W1-11-3342, Arizona General Stream Adjudication Bulletin (AZGSAB)) 2018).
The Verde River is one of the largest remaining perennial rivers in the desert Southwest (Averitt et al. 1994). It supports a native fish community; however, populations of these fishes are severely depressed and the river is presently dominated by nonnative species Rogosch et al. 2019). In the 82 km segment of the Wild and Scenic Verde River, from Beasley Flats to Sheep Bridge, native fish capture has recently been exceptionally low. Catch from a recurring Arizona Game and Fish (AZGF) survey in the four years prior to a major flood (2015-2018) averaged 0.63 native fish/km canoe electrofishing. Nonnative fish captures during those same surveys averaged 213.76 fish/km canoe electrofishing (Arizona Game andFish Department (AZGF) 2015, 2018). Additionally, our own pre-flood sampling captured one native fish in ninety sampling units in 2017.
In February 2019, the Verde River experienced a flood with an instantaneous peak flow of 1,416 m 3 /s (USGS gage 09506000; Figure 1). This was the largest flood of the decade, and the second largest flood recorded here since 2000. This flood afforded us an opportunity to examine change to fish community structure and instream habitat features at multiple locations within the Verde River by revisiting previously sampled sites. We asked the following research questions: Would production and recolonization of young be so low as to be virtually undetectable? Would production of young spawned from only a few fish result in the detection of native juveniles at all study reaches surveyed or only at specific locations? Would the flood redistribute instream habitat features and would that change along the river continuum? This research can benefit conservation by adding to the body of evidence that demonstrates the importance of floods to native fishes of the desert Southwest, while investigating the potential for a depauperate native fish community to seed a river with juveniles.

Study site
The Verde River flows for 274 km from its origins at Big Chino Wash (1325 masl) to its terminus at the confluence with the Salt River in central Arizona (402 masl). For the first 200 km the mainstem Verde River is free flowing, at which point it is impounded by Horseshoe Reservoir (Averitt et al. 1994; Figure 2). This unobstructed condition has allowed for the retention of a relatively natural flow regime, which is characterized by a variable and flashy hydrograph and periodic high magnitude (> 283.17 m 3 /s) floods (Averitt et al. 1994;Serrat-Capdevila et al. 2013). The lower $82 km of the Verde River, prior to impoundment in Horseshoe Reservoir, is designated as Wild and Scenic (Public Law 90-542; 16 U.S.C. 1271 et seq.). Historically, twelve native fish species occupied the Verde River , of which five are extant (Roundtail Chub, Sonora Sucker, Desert Sucker, Longfin Dace Agosia chrysogaster, and Speckled Dace Rhyinichthys osculus). The present fish community is dominated by nonnative species, including Red Shiner Cyprinella lutrensis, Black Bass Micropterus spp., Common Carp Cyprinus carpio, Rainbow Trout Oncorhynchus mykiss, Green Sunfish Lepomis cyanellus, Flathead Catfish Pylodictis olivaris, Channel Catfish Ictalurus punctatus, Bullhead Catfish Ameiurus spp. and other members of the sunfish (Centrarchidae) and minnow (Cyprinidae) families.

Data collection
We sampled fish using prepositioned areal electrofishing devices (PAEDs). Prepositioned areal electrofishing devices reduce fright bias, allow for a multispecies analysis, and are useful in quantifying fish abundance as it relates to discrete microhabitat conditions (Bain   al. 1985;Bovee 1986). The motivation for using this sampling gear was to develop habitat models for fishes of the Verde River (Jenney 2020), but these models are beyond the scope of this current manuscript, which is focused on juvenile native fish production following a major flood. The effectiveness of PAEDsand all electrofishing methods (Guy et al. 2009)decreases with increased depth and is most effective in shallow and littoral areas. Therefore, we limited our sampling to shallow water 1.5 m in depth (Bowen and Freeman 1998). Prepositioned areal electrofishing devices provide a repeatable and consistent method of sampling (Ensign et al. 2002), allowing for a direct comparison between sampling events (Bain et al. 1985;Lucas and Baras 2000).
We constructed PAEDs using two steel pipes (1.5 m long, 1.3 cm diameter) that acted as an anode and cathode, separated by 1.0 m, resulting in a 1.5 m 2 immobilization area. The 1.5 m 2 area between the anode and cathode was considered the sampling unit. Each PAED was connected to a 15.24 m, 12-gauge extension cord that was set downstream and connected to a 2,000/1,400 Watt gasoline powered generator (Buffalo Tools, O'Fallon, Missouri). The generator supplied 120 v of alternating current (AC) to each PAED, as measured by a multimeter. We placed the PAED on the streambed with the anode and cathode positioned parallel to streamflow. We allowed the PAED to sit undisturbed for a minimum of 11 min while technicians remained onshore and distant from the PAED to limit frightening fish into or out of the sampling unit. The 11 min wait has been established as sufficient for fish to recolonize holding locations following disturbance (Bain et al. 1985;Nemec et al. 2021). We then energized the sampling unit for a minimum of 15 s as a technician approached the PAED from downstream and netted immobilized fishes. We identified captured fish to species and measured fish to a TL (mm) prior to releasing the individual at, or near, their capture location.
We established three 1,000 m reaches in the Verde River, at Beasley Flats (34.47320, À111.80180), Childs River Access (34.34748, À111.69783), and Sheeps Bridge (34.07768, À111.70755), hereafter referred to as the upper, middle, and lower reaches. The upper reach was $23 km upstream of the middle reach and $82 km upstream of the lower reach. These reaches provided access into the wilderness segment of the river and allowed us to investigate change to the fish community and instream environment along the river continuum. Ninety locations, thirty at each 1,000 m reach, were sampled using the same PAEDs and techniques pre-flood in 2017 (June 27 À 30) and post-flood in 2019 (June 3-28) to obtain discrete samples of the fish community. The locations of the 90 sampling units were randomly selected in 2017 and revisited in 2019. Discharge during sampling averaged 1.27 m 3 /s in 2017 and 1.70 m 3 /s in 2019 (USGS Gage 09506000, $5.6 km downstream from our upper most sampling unit and $75.3 km upstream from the lower most sampling unit).
We measured total depth, flow velocity, substrate composition, and canopy cover within each sampling unit, regardless of whether fish were captured (Bovee 1986;. Methods used to collect habitat data were identical in 2017 and 2019. We measured total depth, and flow velocity at 60% of total depth, in each corner of the PAED using a wading rod with an electromagnetic current meter (Hach, Loveland, Colorado). The four measurements were then averaged to calculate a mean depth and flow velocity for each sampling unit. We categorized substrate according to the modified Wentworth scale (Bain 1999; Boulder >265 mm in diameter; cobble ¼ 64 À 256 mm; pebble ¼ 16 À 63 mm; gravel ¼ 2 À 15 mm; sand ¼ 0.06 À 1.00 mm; silt < 0.059 mm). We randomly placed a 1 m chain with markings every 10 cm within each 1.5 m 2 sampling unit and categorized substrate at each demarcation. We calculated the mode of these ten categorizations to determine the dominant substrate within each sampling unit. We estimated overhead canopy cover using a spherical densiometer, as described in Lemmon (1956). Each densiometer had twenty-four square cells etched onto its surface. We counted the cells that had vegetation present in at least 3/4 of its area and divided that number by the total number of cells to calculate the proportion of overhead canopy cover. We measured canopy cover in four directions, upstream, downstream, towards the right bank, and towards the left bank, and averaged the measurements.

Data analysis
Fish were analyzed by size class. We defined juvenile Roundtail Chub as fish 70 mm TL and subadult/adult fish (hereafter, referred to as adult fish) as Roundtail Chub > 70 mm TL (Brouder 2001). All other fishes were classified as juveniles if 100 mm TL, and adults if > 100 mm TL, based upon methods described in previous research (Rees et al. 2005;Pilger et al. 2010). Red Shiner were analyzed as a single adult grouping. We grouped Largemouth Bass Micropterus salmoides, Smallmouth Bass Micropterus dolomieu, and Redeye Bass Micropterus coosae as one species complex, Black Bass. A concurrent study found that these bass species readily hybridize within the Verde River (Jenney and Peatman 2019, unpublished report), complicating field identification.
To compare catch from 2017 pre-flood sampling to 2019 post-flood sampling, we calculated a relative abundance and a mean catch per PAED for each species and size-class. Count data was nonnormal with an unequal variance, thus violating the assumptions of the paired T-test. Therefore, we used a nonparametric Wilcoxon signed-rank test to test the null hypothesis that there was no difference in mean catch per PAED between the 2017 and 2019 sampling years. This test discards zero-difference values and rank transforms the differences that remain. We also used a simulated permutation test for paired data to validate the results of the Wilcoxon signed-rank test. We tested the null hypothesis that either of the two values of the paired data were equally as likely, and therefore, the sign of the difference (positive or negative) could be reversed without consequence. We then computed a T-statistic for each permuted sample to approximate the distribution of the T-statistic from 100,000 iterations of this test (Eudey et al. 2010). The simulated permutation test provided a reasonable approximation of P-values to validate the P-values derived from the nonparametric test.
We investigated change to habitat features using a series of T-tests where appropriate and Wilcoxon signed-rank tests when the assumptions of a T-test were violated. To investigate change to depth and overhead cover, we tested the null hypothesis that the mean values for each habitat feature were not different between sampling years using paired Ttests. Depth was nonnormally distribution, and therefore, we applied a log-transformation prior to analysis. Though overhead canopy cover was proportional, it was normally distributed and treated as a continuous variable for this paired analysis. Flow velocity and substrate composition were analyzed with a Wilcoxon signed-rank test due to flow velocity being nonnormally distributed and substrate composition being categorical. Additionally, we assigned a numeric code (Bain 1999; 5 ¼ boulder, 4 ¼ cobble, 3 ¼ pebble, 2 ¼ gravel, 1 ¼ sand, 0 ¼ silt) to each sampling unit based on the dominant substrate present. We then calculated a mean of the substrate codes at the sampling reach and overall study-reach. This method is inappropriate for identifying a specific substrate-type but is useful to document a mean change to substrate between sampling years. All statistical analyses were completed using the program R version 3.6.1 (R Core Team 2017).

Fish abundance
We captured a total of 441 fish of 9 species (3 native and 6 nonnative). In 2017, we captured zero fish at 51% (46 of 90 PAEDs) of all sampling units and in 2019 we captured zero fish at 44% (40 of 90 PAEDs) of all sampling units. Species richness increased from 2017 (n ¼ 7) to 2019 (n ¼ 9) due to the appearance of two native species, Roundtail Chub and Sonora Sucker. Additionally, the relative abundance of native fishes increased from 0.6% of the total catch in 2017 to 53% of the total catch in 2019.
The increase in native fishes (P ¼ 0.003) was due to the increased capture of juvenile fishes (Table 1). Juvenile native fishes were absent in 2017, but in 2019, catch of juvenile native fishes was 0.29 fish/PAED; 1.32 fish/PAED; and 0.04 fish/PAED for Roundtail Chub (P ¼ 0.003); Sonora Sucker (P ¼ 0.027) and Desert Sucker (P ¼ 0.317), respectively. Despite this increase, juvenile Roundtail Chub were absent from 88% of sampling units, juvenile Sonora Sucker were absent from 94% of sampling units, and Desert Sucker were absent from 98% of sampling units in 2019. Additionally, 80 of the 119 juvenile Sonora Sucker were captured in a single sampling unit within the upper reach. We captured one adult native fish, a Desert Sucker, in 2017. No other adult native fishes of any species were captured during sampling. Ninetyseven percent of all native fishes were captured at the upper reach (4.80 fish/PAED, SE ¼ 1.696). The remaining 3% of native fishes were captured at the lower reach (0.17 fish/PAED, SE ¼ 0.049). No native fishes were captured at the middle reach in either year.

Habitat availability and distribution
We found no difference in the distribution of habitat features depth (P ¼ 0.494), flow velocity (P ¼ 0.464), or substrate composition (P ¼ 0.859) at the overall study-scale; however, the mean depth increased at the upper reach (P ¼ 0.043), the mean flow velocity decreased at the lower reach (P ¼ 0.049), and the mean substrate size increased at the upper reach (P ¼ 0.017) and decreased at the lower reach (P ¼ 0.037; Table 2). Canopy cover was reduced by 65% at the upper reach (P < 0.001) and nearly 80% at the lower reach (P < 0.001), resulting in a reduction of > 50% at the overall study-reach (P < 0.001).

Discussion
Our observations, combined with conclusions from past research (Craven et al. 2010;Stefferud et al. 2011), suggest that the observed increase to the abundance of juvenile native fishes was due to spawning triggered by the flood of February 2019. First, floods The mean value and standard error are presented for 2017 pre-flood and 2019 post-flood data. The D Mean represents the change in the mean from 2017 to 2019. Change to depth (log-transformed) and overhead canopy cover (treated as a continuous variable) were analyzed via a series of paired T-tests. Flow velocity and substrate composition were analyzed with a nonparametric Wilcoxon signed-rank test. Substrate was analyzed as categorical determined by the dominant substrate type within each sampling unit. We then assigned a numeric code and reported the mean of the substrate codes to track change to substrate between years. (Bain 1999; 5 ¼ Boulder, >265 mm in diameter; 4 ¼ cobble, 64-256 mm; 3 ¼ pebble, 16-63 mm; 2 ¼ gravel, 2-15 mm; 1 ¼ sand, 0.06-1.00 mm; 0 ¼ silt < 0.059 mm). and native fish reproductive success has been linked for many native fishes of the desert Southwest (Tyus and Karp 1989;Minckley and Marsh 2009). No juvenile fish were captured in our 2017 survey or other surveys of the river in the four previous years (Arizona Game andFish Department (AZGF) 2015, 2018) when no major floods occurred. Second, no other large-scale event besides the flood of 2019 occurred between the two-years to trigger spawning on this scale. It should be noted that the flow magnitude required to trigger reproduction is unknown; however, Brouder (2001) found that the CPUE of age-1 Roundtail Chub increased linearly as a function of flow magnitude one-year after a flood.
Following the flood of 2019, juvenile native fishes were abundant relative to previous years, suggesting that a few individuals can seed a river if high magnitude spring flooding occurs. The reseeding we saw was patchy, with most juvenile native juvenile fishes being captured at the upper reach. Juveniles were present at the lowermost site, albeit in low abundance. Sampling reported in this study focused on 90 sampling units surveyed before and after a flood in a paired design. However, we sampled 292 additional sampling units in 2019 which were not included in the analysis presented in this manuscript as they did not share locations with pre-flood sampling units. These efforts resulted in the capture of an additional 263 juvenile Roundtail Chub, 53 juvenile Sonora Sucker, and 34 juvenile Desert Sucker in the $24 km segment of river between the upper and middle reaches reported in this study. An AZGF monitoring program, which surveyed this same $24 km segment, captured one adult native fish in both 2015 and 2018, and juvenile native fishes were not present (Arizona Game andFish Department (AZGF) 2015, 2018). This provides further evidence that juvenile fish production was related to the flood of 2019. Our findings combined with past research (Brouder 2001;Rinne et al. 2004;Stefferud et al. 2011) suggests that, given spring flooding, small numbers of native fishes can naturally reproduce and repopulate a stream. Furthermore, evidence suggests that the production of young fishes resulted from mainstem spawning and not that in tributaries because the largest concentration of juveniles was distant and upstream from major tributaries, native fishes of the desert Southwest have adaptations limiting displacement from natal streams by major flooding (Minckley and Meffe 1987), and the capture of a single 'ripe' adult Roundtail Chub during a concurrent sampling event provides evidence of the spawning potential within the mainstem Verde River (Jenney 2020).
Although juveniles were produced following the flood of 2019, recruitment is uncertain (Stefferud et al. 2011). To that point, an AZGF survey that occurred two years post-flood (2021) encountered only two native fish, one adult Roundtail Chub and one adult Sonora Sucker (relative abundance ¼ 0.28%; personal communication, AZGF, 2021). Predation by nonnative fishes is the primary reason that native fishes of the desert Southwest fail to recruit (Clarkson et al. 2005;Gibson et al. 2015). This is likely the case on the Verde River, as well Rinne and Miller 2006). The continued lack of native fishes of any size-class two years after a large influx of juveniles likely indicates that recruitment is poor and that floods alone are insufficient to recover native fishes.
The differential response observed along the river continuum and among native fishes may be due to species' susceptibility to predation (Clarkson et al. 2005), their ability to cope with habitat alterations (Gibson et al. 2015), and their pre-flood abundance and distribution . Ninety-seven percent of all native fishes were captured at the upper reach. No native fishes of any size-class were captured at the middle reach, and the remaining 3% were captured at the downstream reach. This might suggest that lower in the river, populations of native fishes are too small to reproduce in any meaningful numbers, nonnative fishes are abundant and depredate young fishes that are produced, or a combination of both. Our findings are consistent with previous research that found native fishes to be concentrated in upstream locations ). More pool-like habitat due to a lessening gradient occurs downstream (Franssen et al. 2016) and these environments likely favor nonnative fishes present in the Verde River (Gibson et al. 2015).
The use of PAEDs allowed for consistent and easily repeatable sampling (Bowen and Freeman 1998;Ensign et al. 2002), which facilitated a direct comparison of the fish community between sampling years. However, the use of PAEDs could have resulted in an underestimation of the abundance of fishes inhabiting depths >1.5 m. This would not invalidate our overall conclusions, as juvenile fishes are known to inhabit shallow-water habitats and littoral zones (Travnichek et al. 1995;Baras and Nindaba 1999) within our sampling frame. Furthermore, the utility and efficiency of PAEDs increases when they are used to quantify juvenile fish abundance (Freeman et al. 2001). Prepositioned areal electrofishing devices have been used successfully to evaluated species richness (Branigan et al. 2018), fish density, and the relative abundance of fishes inhabiting shallow-water lotic environments (Travnichek et al. 1995).
Multiple studies have found that Roundtail Chub, Sonora Sucker, and Desert Sucker spawn on the receding limb of the hydrograph following floods. This life-history strategy would enable native fishes to synchronize spawning to periods when spawning habitats, specifically clean gravel substrates in riffles, are maximized (Lytle and Poff 2004;Propst and Gido 2004). Our research, finding a reduction to substrate size at the most downstream sampling location, supports this hypothesis. Additionally, the significant reduction to overhead canopy cover provides evidence that high magnitude floods in the desert Southwest can restructure the river environment. Yet, previous research found no relationship between change to microhabitat characteristics and juvenile fish year-classes (Strange et al. 1993), which may suggest that native fishes are responding to the flow itself, the temperature change associated with such flows (Fraser et al. 2019), or a combination of both, and not to the distribution of habitat features.
Evidence exists of high-magnitude floods selecting against nonnative fishes within the desert Southwest (Minckley and Meffe 1987;Rinne 1994;Whitney et al. 2014). Consistent with these findings, catch of Common Carp, a fish adapted to low flow velocity environments (Butler and Wahl 2010), declined from 2017 to 2019. A similar reduction to Common Carp was observed in Aravaipa Creek, AZ following major flooding (Minckley and Meffe 1987). Alternatively, the annual drawdown of the downstream Horseshoe Reservoir, which occurred prior to sampling in 2017, may have forced Common Carp into the mainstem Verde River, resulting in increased catch. All Common Carp captures from 2017 occurred at the lower reach, closest to the reservoir. In 2019, the drawdown of Horseshoe Reservoir occurred after sampling (Wicke 2020). Common Carp would have had ample space within the reservoir and might not have been forced into the river environment, thus limiting instream captures. The abundance of all other nonnative fishes remained stable between sampling years, suggesting that the flood had no measurable impact on these species (Rinne 1994;Olden and Poff 2005). Species including Black Bass and Red Shiner are tolerant of elevated flow velocities and possess morphological and behavioral pre-adaptationsa fusiform body shape, an ability to withstand elevated flow velocities, a tolerance for rapid changes to water qualitythat likely increased these species' resistance to floods (Edwards et al. 1983;Ward et al. 2003). The reduction to nonnative fishes reported in previous research (Minckley and Meffe 1987) may be exclusive to canyon-bound reaches of small streams where refuge from disruptive flows is sparse (Propst et al. 2008;Ruhi et al. 2016). Our findings are consistent with research from larger rivers within the desert Southwest where the nonnative fish community returned to a preflood level within 8 days of a large flood (Pool and Olden 2015).
Our case study supports research showing the importance of spring floods to native fish production in the desert Southwest. It demonstrates that few fish can seed large numbers of juveniles, though recruitment is uncertain. The failure of large-scale floods to remove nonnative species suggests reducing populations of nonnative fishes by other means, in addition to maintaining spring floods, is important for native fish recruitment (Tyus and Saunders 2000). Past conservation efforts have largely focused on maintaining a minimum baseflow (Neary and Rinne 1998), clearly needed for the survival of fishes. However, a growing body of evidence emphasizes the importance of other flow components (Poff 2018), such as periodic high magnitude floods. Efforts to harvest flood-flow, in addition to baseflow, may interfere with native fish spawning and the reseeding of streams unless the importance of floods is considered.