Climate warming is likely to cause both indirect and direct impacts on the biophysical properties of stream ecosystems especially in regions that support societally important fish species such as Pacific salmon. We studied the seasonal variability and interaction between stream temperature and DO in a low-gradient, forested stream and a glacial-fed stream in coastal southeast Alaska to assess how these key physical parameters impact freshwater habitat quality for salmon. We also use multiple regression analysis to evaluate how discharge and air temperature influence the seasonal patterns in stream temperature and DO. Mean daily stream temperature ranged from 1.1 to 16.4°C in non-glacial Peterson Creek but only 1.0 to 8.8°C in glacial-fed Cowee Creek, reflecting the strong moderating influence glacier meltwater had on stream temperature. Peterson Creek had mean daily DO concentrations ranging from 3.8 to 14.1 mg L−1 suggesting future climate changes could result in an even greater depletion in DO. Mean daily stream temperature strongly controlled mean daily DO in both Peterson (R2=0.82, P<0.01) and Cowee Creek (R2=0.93, P<0.01). However, DO in Peterson Creek was mildly related to stream temperature (R2=0.15, P<0.01) and strongly influenced by discharge (R2=0.46, P<0.01) on days when stream temperature exceeded 10°C. Moreover, Peterson Creek had DO values that were particularly low (<5.0 mg L−1) on days when discharge was low but also when spawning salmon were abundant. Our results demonstrate the complexity of stream temperature and DO regimes in coastal temperate watersheds and highlight the need for watershed managers to move towards multi-factor risk assessment of potential habitat quality for salmon rather than single factor assessments alone.
Citation: Fellman JB, Hood E, Dryer W, Pyare S (2015) Stream Physical Characteristics Impact Habitat Quality for Pacific Salmon in Two Temperate Coastal Watersheds. PLoS ONE 10(7): e0132652. https://doi.org/10.1371/journal.pone.0132652
Editor: James P. Meador, Northwest Fisheries Science Center, NOAA Fisheries, UNITED STATES
Received: April 14, 2015; Accepted: June 17, 2015; Published: July 29, 2015
Copyright: © 2015 Fellman et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All stream physical data are contained within the paper as Supporting Information.
Funding: This study was supported by the Department of Interior Alaska Climate Science Center and the U. S. National Science Foundation (#OIA-1208927).
Competing interests: The authors have declared that no competing interests exist.
Alaska is a globally important wild-salmon producing region , with more than 4,000 natural runs in southeast Alaska alone . Characterizing suitable aquatic habitat for salmon in coastal watersheds is becoming an increasingly important component of watershed management in light of rapid environmental change in the region. The primary drivers of environmental change include: rising air temperatures , changes in the rain/snow fraction of precipitation  and glacier volume loss , all of which have the potential to impact the physical properties of salmon-producing streams. Of particular importance is the potential these environmental changes have for altering thermal regimes in coastal salmon-producing streams in Alaska [6–9].
Temperature is a fundamental control on metabolic activity and the solubility of dissolved gases (e.g., carbon dioxide and oxygen) in streamwater. As a result, shifts in watershed thermal regimes can impact the availability of freshwater habitat for cold-water fish species [10,11]. For salmonids (e.g., salmon and trout), temperatures that exceed their range of tolerance can adversely affect the growth and development, distribution and abundance, migration and behavior at all life stages [12–14]. In addition to temperature, dissolved oxygen (DO) is an important control on inland aquatic habitat for salmonids because DO levels exert a strong influence on salmonid behavior and metabolic activity [13,15]. Low concentrations of DO can be lethal to salmon, however sub-lethal effects are far more common and include impacts to the growth and development of salmon at different life stages, decreased feeding activity, reduced swimming performance and prevention of upstream migration [15–17].
The physical characteristics of streamwater are controlled by numerous factors including air temperature, discharge, streambed processes and topography [10,18,19]. In the Coast Mountains of Alaska, glaciers and seasonal snowcover are particularly important landscape controls on streamwater physical characteristics because meltwater from these cryospheric reservoirs moderates stream temperature during the summer months [8,20–22]. Glaciers can also attenuate the inter-annual variability in discharge by maintaining streamflow during extended periods in the summer runoff season [23,24]. As a result, changes in snow and glacier melt have the potential to substantially influence habitat quality for both adult and juvenile salmon  as well as aquatic macroinvertebrates (e.g.,).
To date, many watershed-scale studies of salmon habitat quality have focused on either stream temperature or DO alone [26,27]. However, multi-factor studies that allow for a mechanistic understanding on the controls of both stream temperature and DO are clearly necessary given the importance of these parameters to salmon habitat quality. Moreover, the independent effects of stream temperature and DO on salmon habitat quality are often difficult to untangle given their interaction with each other and other biophysical controls such as discharge. We used a paired watershed approach to assess the seasonal variability and interaction between stream temperature and DO in two salmon bearing watersheds in coastal southeast Alaska that differ in terms of snow and glacier melt inputs to streamflow. Multiple regression analysis was used to evaluate how the climatically sensitive variables of stream discharge and air temperature influence seasonal patterns in stream temperature and DO. We further assess whether spawning salmon abundance influences streamwater DO via biological oxygen demand. Our results provide insight into the potential impacts of climate warming on habitat quality for salmon in coastal temperate watersheds adjacent to the Gulf of Alaska.
Materials and Methods
Field sampling was conducted under a permit obtained from the United States Department of Agriculture, Tongass National Forest.
The two study watersheds are located near Juneau in northern southeast Alaska (Fig 1). Juneau has a maritime climate with mild winters and cool, wet summers and a mean annual precipitation of 1400 mm at sea level. Extensive glaciation has modified the region leaving heavily incised watersheds with steep slopes but also abundant lowlands characterized by peatlands mixed with coniferous forest.
Cowee Creek (watershed area of 110 km2) contains a hanging glacier complex with 13% of the watershed covered by glacier ice. Average watershed elevation is 638 m with areas of alpine tundra and exposed bedrock at high elevations and a mixed coniferous forest of Picea sitchensis and Tsuga heterophylla in the mid to lower watershed. Cowee Creek is low gradient downstream near the monitoring station, located ~4 km from the watershed outlet to Berners Bay. A thick riparian forest occupies most of the mid to lower reaches of the watershed, although the main channel is not heavily shaded with wetted-widths typically 10–15 m. Non-glacial Peterson Creek has a watershed area of 24 km2 and a mean watershed elevation of 309 m. Peterson Creek contains large areas of forested and unforested peatland (34% watershed wetland coverage) and has a small lake near its headwaters. The vegetation in the remainder of the watershed is similar to the mid to lower watershed in Cowee Creek consisting mainly of a mixed coniferous forest of P. sitchensis and T. heterophylla. The stream channel is partially to heavily shaded, with wetted widths that range from 5–8 m near the monitoring station.
Peterson and Cowee Creeks both have runs of Pacific salmon (Oncorhynchus kisutch, O. keta and O. gorbuscha) lasting from late June through mid-October that vary in spawner density. Salmon carcass densities of O. keta in Peterson Creek during July and August can be as high as 3.5 kg m-2 or 0.5 fish m-2 [28,29]. In Cowee Creek, salmon carcass densities (mostly O. gorbuscha) are unknown although they are substantially lower than in Peterson Creek based on frequent observations from previous years and during the study period. Previous research in both streams has shown that salmon deliver large quantities of nutrients and organic matter to streamwater, particularly during periods of high spawner density in Peterson Creek and to a lesser extent Cowee Creek [28–30].
Mean air temperature at the Juneau airport across the six-month study period (May-October, 2013) was 11.8°C, well above the long term average of 10.8°C, with June and August showing the largest departures above temperature normals. Rainfall for the study period was 904 mm, which was comparable to the long term average of 870 mm at the Juneau airport. Stream physical characteristics (temperature, turbidity and DO) were measured at 1 hour intervals using a YSI Sonde (model 6600) mounted vertically on a t-post driven into the streambed at both Peterson (58.5°N, -134.8°W) and Cowee Creek (58.7°N, -134.9°W). Manual measurements using a hand-held YSI (model 556) and HACH (2100P) turbidimeter were made twice a week to check the high resolution measurements obtained from the YSI Sondes.
Discharge in Cowee Creek was measured at 15-minute intervals across the study period using a stilling well equipped with a pressure transducer (In Situ, Troll 500). The stage-discharge relationship was used to calculate streamflow. Discharge in Peterson Creek is measured by the Alaska Department of Fish and Game. Grab samples for water isotope (δ18O) analysis were collected at each site twice a week in glass bottles with zero headspace. Streamwater δ18O values can be used to assess seasonal differences in the source of streamflow because snow and glacier ice are typically depleted in δ18O relative to groundwater and rainfall [31,32]. Water isotope analysis was performed on a Picarro L2120-I analyzer within one month of collection. The δ18O values are reported in per mil (‰) following normalization to Vienna standard mean ocean water (VSMOW).
We used visual observations and total dissolved nitrogen (TDN) concentrations as an indicator of spawning salmon abundance based on previous research showing that [TDN] is strongly correlated with the presence of salmon carcasses in Peterson Creek . Streamwater grab samples for TDN were collected at least five days per week across the study period from automated water samplers (ISCO) installed on the stream bank near both monitoring stations. Water samples for TDN were immediately filtered upon collection (every 2–4 days) through pre-combusted Whatman GF/F filters (nominal pore size of 0.7 μm) and concentrations were measured via high temperature combustion on a Shimadzu TOC-V CSH-TN analyzer. A mean concentration and standard deviation were generated for the entire study period and values greater than one standard deviation above the mean were considered days where salmon carcasses were abundant in the stream. Using this approach, we estimated that from August 7–31 salmon carcasses were abundant most days in both streams. We used the maximum weekly average temperature (MWAT) as an indicator of stream thermal suitability for salmon [8,33,34]. The MWAT is commonly used temperature criterion in risk assessments of salmon streams because it is a simple and cost effective technique for temperature tolerance estimates (e.g.,).
Regression models to assess controls on stream temperature and dissolved oxygen
We used multiple linear regression (MLR) to assess the influence of air temperature and stream discharge on mean monthly stream temperature (mean of daily temperature from hourly sample intervals averaged over 1 month). We also used MLR to assess how stream temperature and discharge influenced mean monthly DO concentration (mean of daily DO levels from hourly sample intervals averaged over 1 month). Stepwise regression analysis using SPSS software was used for each monthly MLR model, and only those variables significant at P<0.05 were retained. Furthermore, linear regression was used to assess the relationship between mean daily stream temperature and DO using SPSS software. Previous research at both study sites has shown that nonlinear regression models of stream temperature versus air temperature did not improve the fit due to the narrow temperature range of our study streams .
Non-glacial Peterson Creek had a mean daily specific discharge (i.e. runoff) that ranged from <0.01 to 2.18 mm hr-1 showing many rainfall spikes across the sample period (Fig 2A; Table 1; S1 Table). Runoff in Peterson Creek also varied seasonally, with an overall decrease from early May to its summer minimum in late July and an increase during the autumn rainy season. Mean daily runoff in glacial-fed Cowee Creek ranged from 0.09 to 1.12 mm hr-1 showing less variability relative to Peterson Creek (Fig 2A). The coefficient of variation for mean daily runoff was 0.41 for Cowee Creek compared to 1.35 for Peterson Creek.
Streamwater δ18O values averaged -13.0‰ for Peterson Creek and -14.5‰ for Cowee Creek across the study period reflecting differences in the relative contributions of glacial meltwater and precipitation to streamflow (Fig 2B; Table 1). Values for δ18O in Peterson Creek were the most depleted (-14.5 to -15.0‰) in early May and again in early June but increased from mid-June through early September. In contrast, Cowee Creek had δ18O values below -15.0‰ through most of August reflecting the contribution of glacier meltwater (average = -16.4‰; ) to streamflow, with values only becoming more similar to the seasonal mean δ18O signature of rainfall (average = -11.4±0.7‰) in October.
Streamwater physical characteristics
Mean specific conductivity for the study period was comparable between the two watersheds (27.4 μS cm-1 in Peterson Creek and 25.6 μS cm-1 in Cowee Creek) despite showing dramatically different seasonal patterns (Fig 2C; Table 1; S1 Table). Conductivity in Peterson Creek ranged from 15 to 20 μS cm-1 in late spring/early summer, increased substantially to its mid-summer maximum (76.2 μS cm-1) in early August, and then declined sharply in mid-August, with values generally <30 μS cm-1 for the remainder of the monitoring period. In contrast, specific conductivity in Cowee Creek was highest during the spring (May) and fall (Sep-Oct) and consistently low (<25 μS cm-1) during the main glacial runoff period of July and August. Streamwater turbidity was substantially lower in non-glacial Peterson Creek relative to Cowee Creek across the study period (Fig 2D; Table 1; S1 Table). The highest turbidities in Peterson Creek occurred during the fall rainy months of September and October. Cowee Creek had highly variable turbidities reflecting inputs of glacial silt during the summer runoff period and runoff from the forested landscape during large rainstorms.
Mean daily stream temperature in Peterson Creek ranged from 1.1 to 16.4°C across the study period and demonstrated high variability relative to Cowee Creek, where temperature ranged from only 1.0 to 8.8°C (Fig 3A; Table 1; S1 Table). Stream temperature in both watersheds generally tracked air temperatures, although the pattern was strongly muted in Cowee Creek compared to Peterson Creek. The MWAT, which was used to evaluate thermal habitat quality for salmon, was 14.9°C for Peterson Creek and 8.6°C for Cowee Creek. The MWAT occurred in early August in Cowee Creek coinciding with the period of time spawning salmon were in the stream (Fig 3A). In Peterson Creek, the MWAT occurred in mid-June (16–22 of June) coincident with the warmest air temperatures of the summer.
The two vertical solid lines correspond to the period of time when spawning salmon were abundant in the study streams.
Mean daily concentrations of DO in Peterson Creek ranged from 3.8 to 14.1 mg L-1 showing dramatic seasonal variation across the study period (Fig 3B; Table 1; S1 Table). Mean daily DO in Peterson Creek was lowest (3.8 to 8.9 mg L-1) during August when discharge was generally low and spawning salmon were abundant in the stream and highest during May and October when stream temperature was lowest (Fig 3B). In contrast, mean daily concentrations of DO in Cowee Creek showed relatively little seasonal variation across the study period ranging from 11.1 to 13.2 mg L-1.
Seasonal controls on stream temperature and dissolved oxygen
Mean daily stream temperature was strongly correlated with mean daily DO in both Peterson (R2 = 0.82, P<0.001; Fig 4A) and Cowee Creek (R2 = 0.93, P<0.001; Fig 4B). However, this correlative relationship in Peterson Creek was driven by the highly significant (R2 = 0.90, P<0.001) relationship between DO concentration for stream temperatures <10°C (Fig 5A). On days when stream temperatures were >10°C, DO was mildly related to stream temperature (R2 = 0.15, P>0.001) and relatively strongly influenced by discharge (R2 = 0.46, P<0.001; Fig 5B). These results suggest that the relationship between DO and stream temperature/discharge is best expressed by a piecewise regression, with a stream temperature break point of ~10°C, below which DO concentrations are influenced by stream temperature and above which discharge is a stronger control. Interestingly, concentrations of DO in Peterson Creek were particularly low (<5.0 mg L-1) on days discharge was low and spawning salmon were abundant (Fig 5B).
The four discharge (Q) quartiles divide mean daily discharge into four quarters and “salmon” refers to days when spawning salmon carcasses were abundant in the stream.
Multiple linear regression models showed that air temperature and discharge were strong predictors of mean monthly stream temperature in both Peterson and Cowee Creeks (Table 2). However, in some months (e.g., July and September), discharge did not improve the model fit leaving air temperature alone as the significant predictor of stream temperature at both sites. The most robust stream temperature models in Peterson Creek were typically the spring and fall months (except October), while in Cowee Creek the model was strongest in June-Sept. Mean monthly DO concentrations in Peterson Creek were significantly related to stream temperature and/or discharge for all months, with the strongest (May) and weakest (August) models explaining 99% and 45% of the variance, respectively (Table 2). In Cowee Creek, stream temperature and to a lesser extent discharge were strong predictors of mean monthly DO concentrations in all months except September.
Non-glacial Peterson Creek had high variability in specific discharge across the study period relative to glacial-fed Cowee Creek, emphasizing how runoff from mountain glaciers attenuates seasonal variability in discharge [23,24,36]. The patterns in discharge were consistent with the δ18O signatures for both streams, where snow and glacial meltwater inputs to Cowee Creek resulted in δ18O values remaining depleted (<-15.0‰) well into August. In contrast, δ18O values in Peterson Creek increased during this same period and became more similar to the δ18O signature of rainfall in the study area . The winter snowpack in Peterson watershed was mostly ablated by early summer, leaving rainfall/groundwater as the main sources of streamflow for the remainder of the monitoring period. Together, these results elucidate how seasonally evolving sources of streamwater influence the timing and magnitude of discharge and highlight how watershed hydrology differs between non-glacial streams, where discharge is driven by summer precipitation, and glacial streams, where discharge is strongly influenced by the energy balance at the glacier surface [23,37].
Controls on seasonal stream temperature and dissolved oxygen
The results of our multiple regression analysis for mean monthly stream temperature are consistent with other studies of forested watersheds showing that air temperature [38,39] and to a lesser extent discharge [7,40] are moderate to strong controls on seasonal stream temperature. However, for some months (e.g., August and October) when discharge and air temperature are only mildly related to stream temperature, other variables such as watershed landcover are likely important. For instance, glacier coverage and lake area have been shown to be tightly linked to stream temperature in Southeastern  and Southcentral Alaska [6,41] as well as other regions [21,26,42]. Glaciers are a particularly strong landscape control on stream temperature, with previous studies of proglacial streams observing a decrease in water temperature of 1.1 to 1.2°C for each 10% increase in glacier coverage [8,21]. Thus, glacier meltwater provides a thermal buffering relative to non-glacial streams [8,21,43] that might become increasingly important in the coming decades given projected regional changes in air temperature (increase of >2C° by 2080s) and the areal coverage of seasonal snow (decrease of 22–58% by 2080; ).
Seasonal concentrations of DO in Cowee Creek showed little variability across the study period suggesting that glacier meltwater had a stabilizing effect on DO by moderating stream temperature (always <10°C) and maintaining streamflow volume, thus preventing the seasonal depletion of DO observed in non-glacial Peterson Creek. Concentrations of DO in Peterson Creek were strongly related to stream temperature below 10°C (R2 = 0.90, P<0.001), but were mildly related to stream temperature (R2 = 0.15, P<0.001) and strongly related to discharge (R2 = 0.46, P<0.001) when temperature exceeded 10 ºC. During periods of low flow, reduced streamwater turbulence can contribute to DO depletion by decreasing the vertical mixing that facilitates streamwater oxygenation . In addition, low flow periods increase the thermal sensitivity of the stream to elevated air temperatures by decreasing the thermal mass of streamwater. The impacts of reduced mixing and elevated stream temperatures associated with reduced streamflow are additive in terms of reducing streamwater DO. In Peterson Creek, the % saturation of streamwater DO was regularly below 75% on days when stream temperature exceeded 10°C and streamflow was relatively low (<20 cfs), but close to saturation when temperature was below 10°C. These results highlight the idea that future DO depletion events in small coastal streams will likely be driven by changes in hydrology in addition to atmospheric warming.
The seasonal DO depletion observed in Peterson Creek also appears to be influenced by biotic factors. Maximum DO depletion occurred during mid-August when discharge was extremely low and spawning salmon (live and dead) were abundant based on streamwater TDN concentrations. Ecosystem respiration (ER) in salmon streams of Alaska has been shown to peak when spawning salmon densities are highest likely a result of salmon themselves stimulating ER [45,46]. Moreover, this salmon-induced spike in ER can result in a dramatic decrease in DO  suggesting elevated ER driven by the presence of salmon likely contributed to DO depletion in Peterson Creek during August particularly on days when streamflow was low. Spawning salmon did not appear to have any impact on DO concentrations in Cowee Creek, likely because of the substantially lower density of spawning fish relative to streamflow volume. Overall, our results suggest that multiple interacting physical (stream temperature and discharge) and biotic (salmon) factors control seasonal DO patterns in Peterson Creek.
Stream habitat quality for Pacific salmon
Stream temperature and DO regimes are strong controls on potential freshwater habitat quality for salmon. Controlled laboratory studies and growth models for salmon at various life stages have produced well-defined physiological tolerances for temperature and DO [47–49]. However, these standards may not be directly applicable to evaluate salmon habitat quality because stream ecosystems exhibit some of the most dynamic habitat conditions in nature  and salmon are able to adjust to spatio-temporal changes in habitat variability by migrating to more favorable habitat when necessary [13,51,52]. For instance, juvenile salmon have been shown to occupy different thermal habitats depending on streamflow  and the presence of zones of DO depletion  or to increase their assimilative capacity . Moreover, our data are limited in temporal and spatial extent and thus, our results represent a first approximation of suitable freshwater habitat for salmon.
There were clear inter-stream differences in potential habitat quality for salmon. In particular, the optimal range in MWAT for salmon development is12.8–14.8°C based on growth metrics for salmon at different life stages . The MWAT we measured for Cowee Creek (8.6°C) falls 4.2°C below the optimal range for salmon indicating that on a regional basis, glacier runoff can contribute to sub-optimal physical habitat (e.g., cold and turbid) for salmon [8,53,54]. In contrast, Peterson Creek was at the high end of the optimal range for salmon physiology consistent with other studies in Southeastern  and Southcentral Alaska [6,41] showing that low gradient forested watersheds currently provide favorable thermal habit for salmon. However, the regression slope of mean daily stream temperature against mean daily air temperature in Peterson Creek was 0.78, indicating fairly high sensitivity to future increases in air temperature .
In Peterson Creek, there were four days where mean daily DO was <5 mg L-1, which is the threshold where DO levels generally start to impact salmon behavior (e.g., avoidance; [51,55,56] and metabolic activity [57,58] as well as prevent upstream migration . Concentrations of DO below 5.0 mg L-1 have also been reported to cause mortality and negatively impact aquatic macroinvertebrate communities [19,59]. Therefore, low DO concentrations could impact freshwater habitat quality for salmon directly and also indirectly through increased macroinvertebrate mortality, which is likely an important food source for juvenile coho (O. kisutch) salmon in the stream. Although the low DO episodes observed during August in Peterson Creek were likely too short in duration to cause dramatic impacts to aquatic habitat quality, these values are bordering the critically low range such that climate warming that results in an increase in the frequency and duration of DO depletion could cause sub-lethal and potentially lethal impacts to aquatic species. For instance, if climate change causes summertime stream temperatures to increase only slightly or if more extensive periods of low flow become more common in lower elevation forested streams like Peterson Creek (e.g.,), DO levels could fall into the critically low range for more extensive periods of time, degrading habitat quality for aquatic species. Moreover, salmon-induced spikes in stream ER could result in depressed DO values when spawner densities are high (e.g., ), although this is most likely an additive impact during periods of low streamflow rather than a top-down control on stream DO. Ultimately, developing quantitative models that allow for projections of stream temperature and hydrologic conditions and their interactions with each other and biotic factors (e.g., elevated ER when spawning salmon are present), are clearly necessary for understanding how freshwater habitats that support salmon in the region will be impacted by climate warming.
Future changes in aquatic ecosystems
Coastal Mountain glaciers of southeast Alaska are currently experiencing high rates of mass loss [61,62] and are projected to continue losing mass at rapid rates in the future . Future decreases in glacier volume will impact streamflow regimes by driving a transient increase in meltwater inputs to streamflow (cooling stream temperature) that is followed by a long-term decrease in runoff [23,24,36]. Our findings suggest that as glacier runoff declines and streams undergo a shift in the dominant source of streamwater towards seasonal snowmelt and rainfall, more variable temperature and DO regimes will prevail [64,65]. The greatest changes in discharge and stream physical properties are likely to occur in mid to late summer following melting of seasonal snowpacks, as exemplified by the extended periods of low flow and DO depletion in non-glacial Peterson Creek during mid-July through August. This period of time corresponds to the peak of salmon spawning in watersheds along the Gulf of Alaska. Taken together, our findings support the notion that some salmon runs (heavily glaciated watersheds) might benefit from future climate warming but others (low gradient forested watersheds) might experience declines [66,67].
Climate-driven changes in streamflow timing [9,60] have the potential to dramatically alter the biophysical characteristics of stream ecosystems. While there has been considerable attention aimed at understanding the effects of flow reduction on upstream salmon migration  and macroinvertebrate communities , less attention has focused on the effects of flow reduction on DO regimes (except see ). Our findings suggest that severe low flows may also indirectly affect aquatic species through DO depletion caused by decreased vertical mixing of oxygen. Moreover, decreasing streamflow would be accompanied by a decrease in streamwater albedo thereby facilitating greater in-stream absorption of solar radiation and increasing stream temperature .
Stream temperature response to climate warming has become a pressing environmental issue in some regions of the world, such as the European Alps and the Pacific Northwest of the USA because warmer temperatures are already negatively impacting available habitat for cold-water fish species [67,71,72]. Although the health of salmon runs are not determined from individual factors alone (e.g., tradeoff between food availability, physiology and physicochemical properties; ), standards are necessary for scientists and managers to evaluate the potential effects of climate warming on salmon streams. Our finding that DO regimes can result from interacting physical and biologic controls highlights the complexity of salmon habitat abiotic factors in coastal temperate watersheds. Overall, our results highlight the need for watershed managers to move towards multi-factor risk assessment of potential freshwater habitat quality for salmon rather than single factor assessments alone.
We thank Kim Homan for map preparation and Jarrod Sowa with the Alaska Department of Fish and Game for streamflow data in Peterson Creek.
Conceived and designed the experiments: JBF EH. Performed the experiments: JBF EH WD. Analyzed the data: JBF EH WD SP. Contributed reagents/materials/analysis tools: JBF EH WD SP. Wrote the paper: JBF EH WD SP.
- 1. Knapp G, Roheim C, Anderson J. The great salmon run: Competition between wild and farmed salmon. Washington, DC: World Wildlife Fund; 2007.
- 2. Halupka KC, Bryant MB, Willson MF, Everest FH. Biological characteristics and population status of anadromous salmon in southeast Alaska. Juneau, AK: USDA Forest Service, Pacific Northwest Research Station; 2002. Report No.: PNW-468.
- 3. Arendt A, Walsh J, Harrison W. Changes of Glaciers and Climate in Northwestern North America during the Late Twentieth Century. J Clim. 2009;22: 4117–4134.
- 4. McAfee SA, Walsh J, Rupp TS. Statistically downscaled projections of snow/rain partitioning for Alaska. Hydrol Process. 2014;28: 3930–3946.
- 5. Radić V, Bliss A, Beedlow AC, Hock R, Miles E, Cogley JG. Regional and global projections of twenty-first century glacier mass changes in response to climate scenarios from global climate models. Clim Dyn. 2013;42: 37–58.
- 6. Mauger S. Stream temperature monitoring network for Cook Inlet salmon streams 2008–2010. Homer, AK: Cook Inletkeeper; 2011. Report No.: 11–01.
- 7. Lisi PJ, Schindler DE, Bentley KT, Pess GR. Association between geomorphic attributes of watersheds, water temperature, and salmon spawn timing in Alaskan streams. Geomorphology. 2013;185: 78–86.
- 8. Fellman JB, Nagorski S, Pyare S, Vermilyea AW, Scott D, Hood E. Stream temperature response to variable glacier coverage in coastal watersheds of Southeast Alaska. Hydrol Process. 2014;28: 2062–2073.
- 9. Shanley CS, Albert DM. Climate Change Sensitivity Index for Pacific Salmon Habitat in Southeast Alaska. PLOS ONE. 2014;9: e104799. pmid:25127398
- 10. Caissie D. The thermal regime of rivers: a review. Freshw Biol. 2006;51: 1389–1406.
- 11. Webb BW, Hannah DM, Moore RD, Brown LE, Nobilis F. Recent advances in stream and river temperature research. Hydrol Process. 2008;22: 902–918.
- 12. Brett JR. Energetic Responses of Salmon to Temperature. A Study of Some Thermal Relations in the Physiology and Freshwater Ecology of Sockeye Salmon (Oncorhynchus nerkd). Integr Comp Biol. 1971;11: 99–113.
- 13. Matthews KR, Berg NH. Rainbow trout responses to water temperature and dissolved oxygen stress in two southern California stream pools. J Fish Biol. 1997;50: 50–67.
- 14. Armstrong JB, Schindler DE, Ruff CP, Brooks GT, Bentley KE, Torgersen CE. Diel horizontal migration in streams: Juvenile fish exploit spatial heterogeneity in thermal and trophic resources. Ecology. 2013;94: 2066–2075. pmid:24279277
- 15. Geist DR, Abernethy CS, Hand KD, Cullinan VI, Chandler JA, Groves PA. Survival, Development, and Growth of Fall Chinook Salmon Embryos, Alevins, and Fry Exposed to Variable Thermal and Dissolved Oxygen Regimes. Trans Am Fish Soc. 2006;135: 1462–1477.
- 16. Davis GE, Foster J, Warren CE, Doudoroff P. The Influence of Oxygen Concentration on the Swimming Performance of Juvenile Pacific Salmon at Various Temperatures. Trans Am Fish Soc. 1963;92: 111–124.
- 17. Alabaster JS. The dissolved oxygen and temperature requirements of king salmon, Oncorhynchus tshawytscha, in the San Joaquin Delta, California. J Fish Biol. 1989;34: 331–332.
- 18. Milner AM, Brown LE, Hannah DM. Hydroecological response of river systems to shrinking glaciers. Hydrol Process. 2009;23: 62–77.
- 19. Graeber D, Pusch MT, Lorenz S, Brauns M. Cascading effects of flow reduction on the benthic invertebrate community in a lowland river. Hydrobiologia. 2013;717: 147–159.
- 20. Dorava JM, Milner AM. Role of lake regulation on glacier-fed rivers in enhancing salmon productivity: the Cook Inlet watershed, south-central Alaska, USA. Hydrol Process. 2000;14: 3149–3159.
- 21. Moore RD. Stream Temperature Patterns in British Columbia, Canada, Based on Routine Spot Measurements. Can Water Resour J. 2006;31: 41–56.
- 22. Lisi PJ, Schindler DE, Cline T, Scheuerell M, Walsh P. Watershed geomorphology and snowmelt control stream thermal sensitivity to air temperature. Geophys Res Lett. 2014; in review.
- 23. Fleming SW, Clarke GK. Attenuation of High-Frequency Interannual Streamflow Variability by Watershed Glacial Cover. J Hydraul Eng. 2005;131: 615–618.
- 24. Stahl K, Moore RD. Influence of watershed glacier coverage on summer streamflow in British Columbia, Canada. Water Resour Res. 2006;42: W06201.
- 25. Brown LE, Hannah DM, Milner AM. Vulnerability of alpine stream biodiversity to shrinking glaciers and snowpacks. Glob Change Biol. 2007;13: 958–966.
- 26. Hrachowitz M, Soulsby C, Imholt C, Malcolm IA, Tetzlaff D. Thermal regimes in a large upland salmon river: a simple model to identify the influence of landscape controls and climate change on maximum temperatures. Hydrol Process. 2010;24: 3374–3391.
- 27. Sear DA, Pattison I, Collins AL, Newson MD, Jones JI, Naden PS, et al. Factors controlling the temporal variability in dissolved oxygen regime of salmon spawning gravels. Hydrol Process. 2014;28: 86–103.
- 28. Mitchell NL, Lamberti GA. Responses in dissolved nutrients and epilithon abundance to spawning salmon in Southeast Alaska streams. Limnol Oceanogr. 2005;50: 217–227.
- 29. Hood E, Fellman J, Edwards RT. Salmon influences on dissolved organic matter in a coastal temperate brown-water stream: An application of fluorescence spectroscopy. Limnol Oceanogr. 2007;52: 1580–1587.
- 30. Fellman JB, Hood E, Spencer RGM, Stubbins A, Raymond PA. Watershed Glacier Coverage Influences Dissolved Organic Matter Biogeochemistry in Coastal Watersheds of Southeast Alaska. Ecosystems. 2014;17: 1014–1025.
- 31. Rietti-Shati M, Yam R, Karlen W, Shemesh A. Stable isotope composition of tropical high-altitude fresh-waters on Mt. Kenya, Equatorial East Africa. Chem Geol. 2000;166: 341–350.
- 32. Mark BG, Mckenzie JM. Tracing Increasing Tropical Andean Glacier Melt with Stable Isotopes in Water. Environ Sci Technol. 2007;41: 6955–6960. pmid:17993134
- 33. Nelitz MA, MacIsaac EA, Peterman RM. A Science-Based Approach for Identifying Temperature-Sensitive Streams for Rainbow Trout. North Am J Fish Manag. 2007;27: 405–424.
- 34. Moore RD, Nelitz M, Parkinson E. Empirical modelling of maximum weekly average stream temperature in British Columbia, Canada, to support assessment of fish habitat suitability. Can Water Resour J. 2013;38: 135–147.
- 35. Eaton JG, McCormick JH, Goodno BE, O’Brien DG, Stefany HG, Hondzo M, et al. A Field Information-based System for Estimating Fish Temperature Tolerances. Fisheries. 1995;20: 10–18.
- 36. Stahl K, Moore RD, Shea JM, Hutchinson D, Cannon AJ. Coupled modelling of glacier and streamflow response to future climate scenarios. Water Resour Res. 2008;44: W02422.
- 37. Fountain AG, Tangborn WV. The Effect of Glaciers on Streamflow Variations. Water Resour Res. 1985;21: 579–586.
- 38. Kelleher C, Wagener T, Gooseff M, McGlynn B, McGuire K, Marshall L. Investigating controls on the thermal sensitivity of Pennsylvania streams. Hydrol Process. 2012;26: 771–785.
- 39. Krider LA, Magner JA, Perry J, Vondracek B, Ferrington LC. Air-Water Temperature Relationships in the Trout Streams of Southeastern Minnesota’s Carbonate-Sandstone Landscape. JAWRA J Am Water Resour Assoc. 2013;49: 896–907.
- 40. Dugdale SJ, Bergeron NE, St-Hilaire A. Temporal variability of thermal refuges and water temperature patterns in an Atlantic salmon river. Remote Sens Environ. 2013;136: 358–373.
- 41. Kyle R, Brabets T. Water Temperature of Streams in the Cook Inlet Basin, Alaska, and Implications of Climate Change. Report No.: 01–4109. Anchorage, AK: U.S. Geological Survey; 2001 p. 24.
- 42. Imholt C, Soulsby C, Malcolm IA, Hrachowitz M, Gibbins CN, Langan S, et al. Influence of scale on thermal characteristics in a large montane river basin. River Res Appl. 2013;29: 403–419.
- 43. Richards J, Moore RD, Forrest AL. Late-summer thermal regime of a small proglacial lake. Hydrol Process. 2012;26: 2687–2695.
- 44. Shanley C, Pyare S, Goldstein M, Alaback P, Albert D, Beier C, et al. Climate change implications in the northern coastal temperate rainforest of North America. Clim Change. 2015; in review.
- 45. Holtgrieve GW, Schindler DE. Marine-derived nutrients, bioturbation, and ecosystem metabolism: reconsidering the role of salmon in streams. Ecology. 2011;92: 373–385. pmid:21618917
- 46. Levi PS, Tank JL, Rüegg J, Janetski DJ, Tiegs SD, Chaloner DT, et al. Whole-Stream Metabolism Responds to Spawning Pacific Salmon in Their Native and Introduced Ranges. Ecosystems. 2013;16: 269–283.
- 47. Brett JR, Shelbourn JE, Shoop CT. Growth Rate and Body Composition of Fingerling Sockeye Salmon, Oncorhynchus nerka, in relation to Temperature and Ration Size. J Fish Res Board Can. 1969;26: 2363–2394.
- 48. Sullivan K, Martin D, Cardwell R, Toll J, Duke S. An analysis of the effects of temperature on salmonids of the Pacific Northwest with implications for selecting temperature criteria. Portland, OR: Sustainable Ecosystems Institute; 2000.
- 49. Solomon D, Lightfoot G. The thermal biology of brown trout and Atlantic salmon. Report No.: SCHO0808BOLV-E-P. Briston, UK: Environment Agency; 2008. p. 42
- 50. Whited DC, Lorang MS, Harner MJ, Hauer FR, Kimball JS, Stanford JA. Climate, hydrologic disturbance, and succession: Drivers of floodplain pattern. Ecology. 2007;88: 940–953. pmid:17536710
- 51. Spoor WA. Distribution of fingerling brook trout, Salvelinus fontinalis (Mitchill), in dissolved oxygen concentration gradients. J Fish Biol. 1990;36: 363–373.
- 52. Armstrong JB, Schindler DE. Going with the flow: spatial distributions of juvenile coho salmon track an annually shifting mosaic of water temperature. Ecosystems. 2013;16: 1429–1441.
- 53. Hood E, Berner L. Effects of changing glacial coverage on the physical and biogeochemical properties of coastal streams in southeastern Alaska. J Geophys Res. 2009;114.
- 54. Sergeant CJ, Nagorski S. The implications of monitoring frequency for describing riverine water quality regimes. River Res Appl. 2014. https://doi.org/10.1002/rra.2767
- 55. Whitmore CM, Warren CE, Doudoroff P. Avoidance Reactions of Salmonid and Centrarchid Fishes to Low Oxygen Concentrations. Trans Am Fish Soc. 1960;89: 17–26.
- 56. Reynolds WW, Thomson DA. Responses of Young California Grunion, Leuresthes tenuis, to Gradients of Temperature and Light. Copeia. 1974;1974: 747–758.
- 57. Ruggerone G. Differential survival of juvenile sockeye and coho salmon exposed to low dissolved oxygen during winter. J Fish Biol. 2000;56: 1013–1016.
- 58. Carter K. The Effects of Dissolved Oxygen on Steelhead Trout, Coho Salmon, and Chinook Salmon Biology and Function by Life Stage. California Regional Water Quality Control Board, North Coast Region; 2005.
- 59. Connolly NM, Crossland MR, Pearson RG. Effect of low dissolved oxygen on survival, emergence, and drift of tropical stream macroinvertebrates. J North Am Benthol Soc. 2004;23: 251–270.
- 60. Neal EG, Todd Walter M, Coffeen C. Linking the pacific decadal oscillation to seasonal stream discharge patterns in Southeast Alaska. J Hydrol. 2002;263: 188–197.
- 61. Larsen CF, Motyka RJ, Arendt AA, Echelmeyer KA, Geissler PE. Glacier changes in southeast Alaska and northwest British Columbia and contribution to sea level rise. J Geophys Res. 2007;112.
- 62. Berthier E, Schiefer E, Clarke GKC, Menounos B, Rémy F. Contribution of Alaskan glaciers to sea-level rise derived from satellite imagery. Nat Geosci. 2010;3: 92–95.
- 63. Radić V, Hock R. Regionally differentiated contribution of mountain glaciers and ice caps to future sea-level rise. Nat Geosci. 2011;4: 91–94.
- 64. Hannah DM, Kansakar SR, Gerrard AJ, Rees G. Flow regimes of Himalayan rivers of Nepal: nature and spatial patterns. J Hydrol. 2005;308: 18–32.
- 65. Blaen PJ, Hannah DM, Brown LE, Milner AM. Water temperature dynamics in High Arctic river basins. Hydrol Process. 2012;27: 2958–2972.
- 66. Battin J, Wiley MW, Ruckelshaus MH, Palmer RN, Korb E, Bartz KK, et al. Projected impacts of climate change on salmon habitat restoration. Proc Natl Acad Sci. 2007;104: 6720–6725. pmid:17412830
- 67. Rieman BE, Isaak D, Adams S, Horan D, Nagel D, Luce C, et al. Anticipated Climate Warming Effects on Bull Trout Habitats and Populations Across the Interior Columbia River Basin. Trans Am Fish Soc. 2007;136: 1552–1565.
- 68. Trepanier S, Rodriguez MA, Magnan P. Spawning migrations in landlocked Atlantic salmon: time series modelling of river discharge and water temperature effects. J Fish Biol. 1996;48: 925–936.
- 69. Dewson ZS, James ABW, Death RG. A review of the consequences of decreased flow for instream habitat and macroinvertebrates. J North Am Benthol Soc. 2007;26: 401–415.
- 70. Richards J, Moore RD. Discharge dependence of stream albedo in a steep proglacial channel: SCIENTIFIC BRIEFING. Hydrol Process. 2011;25: 4154–4158.
- 71. Hari RE, Livingstone DM, Siber R, Burkhardt-Holm P, Guttinger H. Consequences of climatic change for water temperature and brown trout populations in Alpine rivers and streams. Glob Change Biol. 2006;12: 10–26.
- 72. Isaak DJ, Luce CH, Rieman BE, Nagel DE, Peterson EE, Horan DL, et al. Effects of climate change and wildfire on stream temperatures and salmonid thermal habitat in a mountain river network. Ecol Appl. 2010;20: 1350–1371. pmid:20666254
- 73. Bacon PJ, Gurney WSC, Jones W, Mclaren IS, Youngson AF. Seasonal growth patterns of wild juvenile fish: partitioning variation among explanatory variables, based on individual growth trajectories of Atlantic salmon (Salmo salar) parr: Seasonal growth of salmon parr. J Anim Ecol. 2005;74: 1–11.