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Susitna‐Watana Hydroelectric Project Document
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Title:
Eulachon white paper
SuWa 70
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Prepared by HDR Alaska, Inc.
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2012 Environmental Studies
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Susitna-Watana Hydroelectric Project document number 70
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[Anchorage, Alaska : Alaska Energy Authority, 2013]
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March 2013
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iii, 19, 2, 4 pages
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Susitna-Watana Hydroelectric Project
(FERC No. 14241)
Eulachon White Paper
Prepared for
Alaska Energy Authority
Prepared by
HDR Alaska, Inc.
March 2013
EULACHON WHITE PAPER
Susitna-Watana Hydroelectric Project Alaska Energy Authority
FERC Project No. 14241 Page i March 2013
TABLE OF CONTENTS
1. Introduction ........................................................................................................................1
2. Description ..........................................................................................................................1
3. Life History .........................................................................................................................2
3.1. Larvae to Juveniles ..................................................................................................2
3.2. Juveniles to Adults ...................................................................................................2
3.3. Adult Migration and Spawning ................................................................................3
3.4. Eggs and Incubation .................................................................................................5
4. Cook Inlet ...........................................................................................................................5
4.1. Kenai River ..............................................................................................................6
4.2. Twentymile River ....................................................................................................6
4.3. Susitna River ............................................................................................................6
4.3.1. Spawning..................................................................................................... 6
4.3.2. Biological Parameters ................................................................................. 7
4.3.3. Spawning Habitat Characteristics ............................................................... 8
5. Importance..........................................................................................................................9
5.1. Subsistence and Personal Use Fisheries ..................................................................9
5.2. Commercial Fishery ...............................................................................................10
5.3. Sport Fishery ..........................................................................................................11
5.4. Biological Importance ............................................................................................13
6. Need for Additional Data ................................................................................................13
7. References .........................................................................................................................14
LIST OF TABLES
Table 4.3-1. Length and weight of pre-spawning condition eulachon captured by dip nets in
the intertidal region from both runs during 1983 and segregated by age and sexa ................. 8
Table 4.3-2. Summarization of eulachon sex ratio by dip net and electrofishing efforts during
1983 between Susitna River mile 4.5 and 60.0a ...................................................................... 8
Table 5.2-1. Commercial harvest of eulachon in the Upper Cook Inlet, 1978–2011 .................. 11
Table 5.3-1. Sport harvest of smelt (number of eulachon and capelin combined) in
Southcentral Alaska, including Upper Cook Inlet and the Susitna River, 2001–2010 ......... 12
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APPENDICES
Appendix A. Figures
Appendix B. Spawning Habitat Characteristics
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LIST OF ACRONYMS AND SCIENTIFIC LABELS
Abbreviation Definition
µmhos micromhos
ADF&G Alaska Department of Fish and Game
AEA Alaska Energy Authority
APA Alaska Power Authority
APA Project APA Susitna Hydroelectric Project
cfs cubic feet per second
CIBW Cook Inlet beluga whales
cm centimeter
CPUE catch per unit effort
ESA Endangered Species Act
FERC Federal Energy Regulatory Commission
FR Federal Register
ft/s feet per second
ILP Integrated Licensing Process
km kilometer
m meter
m3 cubic meter
mg/L milligrams per liter
mm millimeter
m/s meters per second
NEPA National Environmental Policy Act
NMFS National Marine Fisheries Service
ODFW Oregon Department of Fish and Game
Project Susitna-Watana Hydroelectric Project
RM river mile
WDFW Washington Department of Fish and Wildlife
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1. INTRODUCTION
This white paper presents the results of efforts to address portions of two objectives of the 2012
Cook Inlet Beluga Whale Study related to eulachon. Those objectives include:
- Summarize life history, run timing, abundance, distribution, and habitat of beluga whale prey
species (eulachon and adult Chinook, chum, coho, and sockeye salmon) in the Susitna River; and
- Evaluate life history, run timing, abundance, distribution, and habitat of beluga whale prey
species (eulachon and adult Chinook, chum, coho, and sockeye salmon) in other Cook Inlet
tributaries used by beluga whales
The Alaska Energy Authority (AEA) is preparing a License Application that will be submitted to
the Federal Energy Regulatory Commission (FERC) for the Susitna-Watana Hydroelectric
Project (Project) using the Integrated Licensing Process (ILP). The Project is located on the
Susitna River, an approximately 300-mile-long river in Southcentral Alaska. The Project’s dam
site would be located at river mile (RM) 184.
This effort provided data to inform the 2013–2014 licensing study program, Exhibit E of the
License Application, and FERC’s National Environmental Policy Act (NEPA) analysis for the
Project license.
2. DESCRIPTION
Eulachon (Thaleicthys pacificus) are small (less than 250 millimeters [mm] fork length and
weigh 40 to 60 grams) forage fish from the family Osmeridae. They are distributed along the
west coast of North America from the Pribilof Islands and the eastern Bering Sea in Alaska
southward to the Klamath River in California (Scott and Crossman 1973). At least 35 rivers in
Alaska have spawning runs of eulachon (Moffitt et al. 2002), with the Nushagak River being the
northernmost river known to support a spawning population (Mecklenberg et al. 2002).
Eulachon, also known as hooligan or candlefish, are anadromous, meaning adults migrate from
the ocean to spawn in freshwater streams and rivers where their offspring hatch and migrate back
to the ocean to forage until maturity. Although they spend greater than 90 percent of their lives at
sea (Hay and McCarter 2000), available information on eulachon in the ocean environment is
sparse (Stables et al. 2005). In most cases, eulachon spawn once, and then die; however, Scott
and Crossman (1973) found evidence of repeat spawning.
Eulachon are sexually dimorphic with males typically being of greater length and having longer
and wider ventral fins than females (Spangler et al. 2003; Cambria Gordon 2006). Males have
tubercles on the body, head, fins, and particularly the lateral lines (McPhail and Lindsey 1970;
Spangler et al. 2003), and have greater muscle mass along the lateral line than females (Spangler
et al. 2003). In the Twentymile River, Alaska, females have been observed to retain their teeth to
a greater degree than males (Spangler 2002).
Because of their abundance in the Susitna River, eulachon were investigated in association with
the Alaska Power Authority’s (APA) early 1980s hydroelectric efforts on the Susitna River
(APA Project). With the reevaluation of the Project, eulachon are again being studied because of
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their importance as a prey species for Cook Inlet beluga whales (CIBW). The purposes of this
paper are to summarize the information available regarding eulachon life cycles across their
range and examine the information regarding eulachon in glacial systems, focusing on the
Susitna River. This synthesis will also aid in study planning and management decisions for the
Project.
3. LIFE HISTORY
3.1. Larvae to Juveniles
Eulachon start and end their life cycle in fresh water. Newly hatched larvae are transparent,
slender, and poor swimmers. Reported lengths ranged from approximately 4 to 8 mm (Parente
and Snyder 1970; WDFW and ODFW 2001; Hay et al. 2002; Lewis et al. 2002). Because they
are weak swimmers, larvae are rapidly carried downstream to estuarine portions of rivers and
inlets within hours or days of hatching (Smith and Saalfeld 1955; Parente and Snyder 1970;
Samis 1977; Howell 2001). Larval eulachon may remain in low salinity surface waters of
estuaries for several weeks or longer (Hay and McCarter 2000), especially in inlets or fjords
(McCarter and Hay 1999; 2003).
Both the short time eulachon larvae spend in fresh water and their small size when reaching salt
water likely preclude their ability to imprint on a spawning river (McCarter and Hay 1999; Hay
and McCarter 2000). However, eulachon larvae and juveniles may spend weeks to months in
nearby estuarine environments where they grow significantly in size and may develop the
capacity to imprint on large estuaries and eventually home to these areas as adults (McCarter and
Hay 1999; Hay and McCarter 2000). From April to August, larval eulachon on the central British
Columbia coast were estimated to grow to 30 to 35 mm in length (McCarter and Hay 1999;
2003). Large river estuaries, inlets, and fjords may therefore serve as the smallest stock structure
unit for eulachon (McCarter and Hay 1999; 2003; Hay and McCarter 2000; Hay 2002; Hay and
Beacham 2005).
Most eulachon larvae have been found in the top 15 m of the water column, with few found
below 20 m (McCarter and Hay 1999; Hay and McCarter 2000). Robinson et al. (1968)
determined that almost all eulachon larvae in the Strait of Georgia, off the Fraser River, were
distributed in the top 6.5 m of the water column. Larval eulachon were usually located near the
bottom during their downstream migration in the lower Columbia River (Smith and Saalfeld
1955; Howell et al. 2001), but were distributed throughout the water column in the Fraser River
estuary (Levings 1980).
3.2. Juveniles to Adults
Eulachon that range from 30 to100 mm in length, exhibit schooling behavior, and have
developed pigmentation and lateral scales are generally classified as juveniles (Hay and
McCarter 2000). Once juvenile eulachon enter the ocean environment, they move from shallow
nearshore areas to deeper areas over the continental shelf. Hay and McCarter (2000) reported
that juveniles dispersed to open, marine waters within one year and perhaps within the first few
months. Eulachon juveniles feed on zooplankton, eating chiefly crustaceans such as copepods,
euphausiids, malacostracans, and cumaceans (76 FR 65324).
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Little information is available about eulachon movements in nearshore marine areas and the open
ocean because they are too small to occur in most fisheries and too large to occur in
ichthyoplankton surveys (Hay and McCarter 2000). However, eulachon occur as bycatch in the
ocean shrimp (Pandalus jordani) fishery, indicating that the distributions of these two species
overlap (76 FR 65324). Barraclough (1964) sampled juvenile eulachon in the Strait of Georgia in
winter and spring with midwater trawls and shrimp trawls and learned that at least some portion
of first year Fraser River eulachon were present. Few eulachon were caught as bycatch in the
late 1990s in the Strait of Georgia shrimp fishery (Hay et al. 1999); however, a larger mesh size
is used in commercial shrimp trawls compared to the mesh size used by Barraclough (1964).
Thus, although they may be present in coastal waters, juvenile eulachon have been difficult to
detect without a directed effort.
Because of their high lipid content, juvenile and adult eulachon are a valuable prey item (Hay
and Boutillier 1999). Several marine mammal species feed upon juveniles and adults, and
spawning runs may be may be preyed upon by several bird, mammal, and fish species.
3.3. Adult Migration and Spawning
After spending several years at sea continuing to feed on crustaceans, eulachon return to the
freshwater environment to spawn. Seasonal entry into spawning rivers appears related to water
temperature and the occurrence of high tide (76 FR 65324). Eulachon are fundamentally
semelparous, spawning once and then dying, although some individuals may survive to spawn
twice. The frequency of iteroparity (multiple spawning) in various populations is not well
understood (Hay and McCarter 2000; Lewis et al. 2002).
Hay and McCarter (2000) and Cambria Gordon (2006) found no clear latitudinal or other pattern
in eulachon spawn timing. The temperature at which eulachon spawning runs commenced varied
by geographic area; however, a clear pattern was not readily discernible (Spangler 2002).
Eulachon spawned as early as January in rivers of the Copper River delta of Alaska (Moffitt et
al. 2002), as late as May in northern California, and from January to April in various reaches of
the Columbia River. In Southeast Alaska, spawning migrations can occur in April, with the
Chilkat and Alsek rivers having occasional winter runs in January and February. Spawning
migrations generally occur in May in Central and Western Alaska. Moody (2008) found that the
analysis of spawn timing as a stock identifier in eulachon was complicated by observed variation
in the duration of spawning from year to year, the presence of multiple spawning runs in some
rivers, and observations of eulachon returning earlier in recent years in some systems relative to
historical data.
Eulachon appear to use streams in the general area where they were spawned that have the best
habitat conditions. Abundance in a particular stream can vary greatly from year to year
depending on water conditions and overall ocean survival (Emmett and Brodeur 2000). Some
streams can have two overlapping runs (ADF&G 2008).
Although timing and duration of eulachon spawning migrations in Alaska have been studied
(ADF&G 1984; Spangler et al. (2003), information on the amount of time spent in fresh water by
individual fish is sparse. Spangler et al. (2003) used radio telemetry to help characterize the
spawning migration in the Twentymile River, and noted that individual fish spent relatively little
time in fresh water, similar to rainbow smelt (4-10 days). Time spent in larger rivers is
unknown.
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Eulachon spawning rivers are typically slow moving because eulachon are weak swimmers that
cannot travel through long stretches of high water velocity. Water velocity greater than 0.4
meters per second (m/s) may limit upstream movements (Lewis et al. 2002). Most spawning in
the Susitna River occurred at water velocities of 0.15 to 0.75 m/s (Vincent-Lang and Queral
1984).
Spawning sites are in the lower elevations of most rivers, but in some rivers with long, flat
deltas, spawning sites may be many miles upstream. Spawning in many rivers is often limited to
areas of tidal influence (Lewis et al. 2002). Eulachon have been reported to go as far as 80
kilometers (km) up the Susitna River (Barrett et al. 1984; Vincent-Lang and Queral 1984), and
once ascended more than 160 km in the Columbia River system.
Eulachon spawning rivers may be turbid or clear, but all are thought to have spring freshets,
characteristic of rivers draining large snow packs or glaciers (Hay and McCarter 2000). In
general, eulachon spawned at low water levels prior to spring freshets (Lewis et al. 2002),
although runs in the Fraser River occurred at mid-levels of river discharge (Langer et al. 1977).
Spawning sites varied among years within the same river system (Pedersen et al. 1995; Hay and
McCarter 2000; Moffitt et al. 2002). Spawning substrates ranged from silt, sand, or gravel to
cobble and detritus (Smith and Saalfeld 1955; Barrett et al. 1984; Vincent-Lang and Queral
1984), but sand was most common (Langer et al. 1977; Lewis et al. 2002).
Size of adult eulachon returning to spawn may vary among areas and years, with fish in Alaska
generally being larger than fish from southern populations (Gustafson et al. 2010). The
maximum known length for eulachon is 254 mm (Mecklenberg et al. 2002). Mean lengths of
spawning eulachon from Alaska populations exceed 175 mm, whereas mean lengths from the
Columbia River generally have been less than 175 mm (Gustafson et al. 2010). Males are usually
slightly larger than females.
Although age determination of eulachon is difficult and uncertain, adult spawners have been
reported to be 2 to 5 years-old (Smith and Saalfeld 1955; Hay and McCarter 2000; WDFW and
ODFW 2001; Hay 2002; Hay et al. 2005; Schweigert et al. 2007). Based on seasonal fluctuations
in barium and calcium concentrations in otoliths, Clarke et al. (2007) concluded that many
eulachon have been aged incorrectly. Clarke et al. (2007) found only 3-year-old eulachon in the
spawning populations in the Fraser and Kemano rivers, and found that the majority of fish for the
Columbia, Skeena, and Copper rivers were primarily 2-, 3-, and 4-year-olds, respectively. These
data suggest that southern populations spawn at an earlier age than northern populations.
Gustafson et al. (2010) reported that sex ratios of spawning fish varied, but males often
outnumbered females. Spawning occurred at night (Hay and McCarter 2000; Lewis et al. 2002)
or afternoon (Langer et al. 1977), at various depths depending on the river. The sexes must
synchronize their activities closely, because eulachon sperm may remain viable for only a short
time, perhaps only minutes (Hay and McCarter 2000). Lewis et al. (2002) described spawning
behavior wherein males took positions either beside or on top of females. This description differs
markedly from that in Langer et al. (1977), wherein males congregated upstream of groups of
females and released milt simultaneously, and females laid eggs as the milt drifted over them.
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3.4. Eggs and Incubation
Fecundity of spawning females may vary with respect to geography or among years, but no
pattern is apparent. As expected, fecundity tends to increase with increasing fish length.
Numerous studies found mean fecundity for “average size females” to be 25,000 to 35,000 eggs
(Gustafson et al. 2010).
The reported size of eulachon eggs has varied slightly among studies. All reports indicated that
the diameter of mature eggs ranged from approximately 0.75 to 1.02 mm (Parente and Snyder
1970; WDFW and ODFW 2001; Hay and McCarter 2000; Hay et al. 2002; HDR 2008). Mature
eggs have an outer sticky membrane that turns inside out after being fertilized and remains
attached to the egg by a short stalk, by which the egg adheres to particles of sand or other
substrates (Hart and McHugh 1944: Smith and Saalfeld 1955: Hay and McCarter 2000). Eggs
may drift downstream for a short time before adhering to the substrate. Even after adhering,
water velocity may continue moving them downstream while they develop (Lewis et al. 2002).
Spangler (2002) and Spangler et al. (2003) noted that, in general, the incubation requirements for
eulachon eggs appeared to increase with increasing latitude. Artificially spawned and incubated
eulachon eggs from the Cowlitz River in Washington hatched in 21 to 25 days when reared
between 6.5°C and 9.0ºC (Parente and Snyder 1970). Berry and Jacob (1998) reported the
incubation period in the Kingcome River in British Columbia to be approximately 21 days. Flory
(2008) indicated that the incubation period for eulachon in Southeast Alaska ranged from 4 to 6
weeks. In the Twentymile River in Southcentral Alaska, incubation was estimated to take 47 to
50 days (Spangler 2002; Spangler et al. 2003).
Egg survival rate may be variable depending on: 1) environmental conditions, 2) whether they
are drifting or accumulating in areas of low velocity, and 3) whether they are exposed to salt
water. Drifting eggs may survive at higher rates than stationary eggs (Lewis et al. 2002);
however, salinity can be lethal (Farara 1996).
4. COOK INLET
Information on eulachon distribution and run timing is limited in Alaska and specifically in the
Cook Inlet; however, eulachon are known to occur in at least nine streams within the Cook Inlet
(Appendix A, Figure 1; Johnson and Blanche 2012).They may also be present near Kalagin
Island, which may serve as a late-winter staging area for eulachon prior to migration to spawning
streams in the Upper Cook Inlet (Figure 1 in Appendix A; NMFS 2010). Eulachon have also
been harvested along the shorelines of Turnagain Arm and the Cook Inlet north of the Ninilchik
River (NMFS 2010). Spangler et al. (2003) found eulachon in a few sampling events during
2000 and 2001 on Portage Creek and Placer River. Spangler et al. (2003) noted that prior to the
1964 earthquake; the Placer River run was much larger than that in Twentymile River. Eulachon
were also found in streams in Trading Bay State Game Refuge; however, these runs have not
been well documented (ADF&G 2012a).
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4.1. Kenai River
Information on eulachon in the Kenai River is limited to presence data (ADF&G 1971; Johnson
and Blanche 2012). Eulachon are present in the Kenai River between late April and late June.
4.2. Twentymile River
In 2000 and 2001, Spangler et al. (2003) used radio telemetr y to examine the migratory behavior
of spawning eulachon and also investigated larval outmigration. They found Twentymile River
to have the longest spawning period of any river for which data are available. They also
determined that males spent more time in freshwater than females. In 2000 the eulachon
spawning migration started May 4 and continued through June 21, whereas in 2001 the migration
began April 17 and continued through June 9.
Spangler et al. (2003) were unable to determine the uppermost extent of eulachon spawning in
the Twentymile River through use of radio telemetry. Juvenile eulachon that would have been
unable to swim upstream were located above the upstream-most documented location of adults.
However, because few larvae were captured upstream, they concluded that most spawning
grounds had been documented. Spangler et al. (2003) noted that radio telemetry was a useful
tool to study eulachon migratory behavior, but should be combined with other methods, such as
larval sampling, to determine upper limits of spawning.
Through examination of otoliths, Spangler et al. (2003) determined that age-2 males occurred
more frequently during the early part of the run each year, whereas age-4 and age-5 males
occurred during the latter part of the run. Age-3 fish dominated both years and were found
throughout the runs. Age classes of females did not vary over time.
Outmigrating larvae were studied by Spangler et al. (2003) and HDR (2006; 2008). Although
Spangler et al. (2003) found larvae over the course of 113 days (May 8 through August 28);
densities were greatest from June 17 through July 20. Similarly, densities in 2006 were greatest
from June 21 through July 12 (HDR 2008). In 2001, larvae were first observed 22 days after
arrival of adults (Spangler et al. 2003). In 2006, larvae were initially most abundant at sampling
sites near the mouth of Twentymile River; however, toward the end of the season they were
more abundant at sites in Turnagain Arm (HDR 2006).
4.3. Susitna River
The most intensive studies on Cook Inlet eulachon occurred during the 1980s Susitna
Hydroelectric evaluation performed by ADF&G under contract to APA (ADF&G 1983a; 1983b;
Barrett et al. 1984; Vincent-Lang and Queral 1984). These studies assessed eulachon spawning,
biology, and spawning habitat characteristics.
4.3.1. Spawning
During the 1980s Susitna Hydroelectric evaluation, ADF&G described two eulachon spawning
runs in the Susitna River, with the second run being considerably larger than the first (Barrett et
al. 1984). In 1982, the first spawning run occurred between May16 and May 30 and the second
run occurred between June 1 and June 8. The run of eulachon was so dense that it appeared to
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create a visible surface wave (ADF&G 1983a). Even though the number of fish was much
greater in the second run, the runs were similar in duration (Barrett et al. 1984).
In 1983, the first run occurred between May 10 and May 17 and the second run occurred
between May 19 and June 6 (Barrett et al. 1984). The spawning run may actually have started
earlier than recorded because migration had begun before sampling started (Vincent-Lang and
Queral 1984). The highest catch per unit effort (CPUE) for both set nets and dip nets occurred on
May 13 for the first run and on May 23 for the second run (Barrett et al. 1984). Vincent-Lang
and Queral (1984) hypothesized that the differences in run timing between years was due to the
surface water temperatures in the Susitna River. The river was warmer in 1983 and thus the
spawning migration began earlier.
ADF&G (1983b) and Barrett et al (1984) conducted research to determine if eulachon spawning
migrations were correlated with surface water temperature, mainstem Susitna River discharge, or
Cook Inlet tidal height, because changes to surface water temperature and mainstem discharge
were identified as potential Project impacts. In 1982, eulachon spawning runs occurred during
increases in both mainstem discharge and surface water temperature (ADF&G 1983b). In 1983,
however, no correlations were found between eulachon abundance, surface water temperature, or
Cook Inlet tidal elevation, although the majority of eulachon movement into the Susitna River
occurred at surface water temperatures between 6.0°C and 9.0°C (Barrett et al. 1984).
4.3.2. Biological Parameters
Morphological characteristics were collected from a subset of eulachon captured during 1982
and 1983 to aid in classifying the biological structure of the eulachon runs. Sex and spawning
condition were determined by observations of milt or eggs (Barrett et al. 1984).
Males:
Pre-spawners—bright coloration and thick milt
Spawners—dark coloration and water milt
Post-spawners—essentially void of milt
Females:
Pre-spawners—eggs were not expelled freely
Spawners—eggs were expelled freely
Post-spawners—essentially void of eggs
Descriptive population information was summarized from 1983 catch data. Both the first and
second runs of eulachon included 2-, 3-, and 4-year-old fish, with 3-year-olds dominating (92.6
percent of males and 97.2 percent of females in the first run; 92.3 percent of males and 92.1
percent of females in the second run; Barrett et al. 1984). For 3-year-olds, first-run males were
longer and weighed more than second-run males (Table 4.3-1; Barrett et al. 1984). Age-3
females from the first run were slightly larger than their counterparts from the second run, but
differences were not statistically significant.
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Table 4.3-1. Length and weight of pre-spawning condition eulachon captured by dip nets in the intertidal region from
both runs during 1983 and segregated by age and sexa
Age Sex Run Sample Size Length (mm) Weight (g)
Range Mean Range Mean
2 M 1 2 191—216 203 50.6—68.8 59.1
3 M 1 50 186—229 212 45.1—86.0 69.1
4 M 1 2 200—222 211 59.4—78.7 69.1
2 F 1 1 195 195 54.3 54.3
3 F 1 35 180—222 203 45.1—74.8 60.2
2 M 2 1 182 182 44.2 44.2
3 M 2 36 187—228 207 44.3—82.8 67.4
4 M 2 2 219—231 225 89.4—93.5 89.6
2 F 2 2 174—193 184 43.4—48.0 47.3
3 F 2 35 186—218 201 48.8—71.3 59.7
4 F 2 1 203 203 60.6 60.6
aTable adapted from Barrett et al. 1984.
Sex ratios differed depending on run and development stage (Table 4.3-2). Pre-spawning males
outnumbered pre-spawning females in the first run, but pre-spawning females outnumbered
males in the second run (Barrett et al. 1984). For spawners and post-spawners, males greatly
outnumbered females. The high ratio of spawning males to females indicated that males matured
earlier and stayed in spawning condition longer than females (Barrett et al. 1984).
Table 4.3-2. Summarization of eulachon sex ratio by dip net and electrofishing efforts during 1983 between Susitna River
mile 4.5 and 60.0a
Development
Stage
First Run Second Run
n
(males) n (females) M:F
ratio
n
(males) n (females) M:F ratio
Pre-spawners 316 253 1.2:1 1,341 2,084 0.6:1
Spawners 1,320 70 18.9:1 3,730 788 4.7:1
Post-spawners 249 16 15.6:1 1,388 403 3.4:1
aTable adapted from Barrett et al. 1984.
4.3.3. Spawning Habitat Characteristics
Susitna River eulachon use a wide array of spawning habitats. Because eulachon are broadcast
spawners their habitat requirements are not as constricted as other species (Morrow 1980). Sites
were determined to be spawning sites by ADF&G (1983c) if the following criteria were met:
Fish freely expelled eggs or milt
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Fish were in vigorous free swimming condition
Twenty or more fish, which met the conditions above, were captured during a sampling
event (ADF&G 1983c).
During 1983, 61 spawning sites were identified in the mainstem Susitna River (Barrett et al.
1984). The first run used 10 sites for spawning and the second run used 57 sites. All sites from
the first run were used for the second run, with the majority (70 percent) of spawning occurring
between river miles (RMs) 12 and 27.
Data from 1982 and 1983 indicated that eulachon preferred areas with moderate downstream
velocities (0.3 to 3.0 ft/s) and were rarely found in low velocity waters (less than 0.3 ft/s),
backwater, or eddies (ADF&G 1983a). Spawning depth averaged 130 cm and ranged from 40 to
170 cm (Appendix B, Table B-1; Vincent-Lang and Queral 1984). Eulachon spawned over a
wide range of substrate types, but most spawning occurred near cutbanks and along riffles with
loose sand and gravel. Because of the increased number of fish in the second run, spawning often
occurred in less desirable habitat (i.e., deeper and higher velocity; Barrett et al. 1984). Eulachon
appeared to utilize turbid water during both years because no spawning occurred in clear water
streams, semi-placid main channel reaches, or sloughs (ADF&G 1983b).
In 1983, ADF&G measured water quality parameters at 20 spawning sites (Appendix B, Table
B-2; Barrett et al. 1984). Water temperature ranged from 6.5°C to 10.8°C, pH ranged from 6.6 to
7.2, specific conductance ranged from 93 to 108 micromhos (µmhos), dissolved oxygen ranged
from 5.9 to 11.3 milligrams per liter, and mainstem discharge ranged from 62,000 to 66,000
cubic feet per second.
The upstream extent of eulachon migration differed little between years (RM 49.5 in 1982 and
RM 50 in 1983; ADF&G 1983a; Barrett et al. 1984). Most spawning occurred for both runs
between RM 8.5 and the Yentna River confluence (RM 28; ADF&G 1983b). During 1982,
eulachon were also observed in the Yentna River, upstream to Big Bend (approximately 8,000
meters upstream of the confluence with the Susitna River). Historically a few eulachon have
been observed in the Yentna River up to the Skwentna River (approximately 23,000 meters
upstream of the confluence with the Susitna River; ADF&G 1983a; see Appendix A, Figure 2).
Recent anecdotal reports indicate possible eulachon presence in the Susitna River up to
Talkeetna (RM 97); however, reliability of these reports is unknown, and they have not been
validated by ADF&G.
5. IMPORTANCE
5.1. Subsistence and Personal Use Fisheries
Eulachon are highly important ceremonially, nutritionally, medicinally, and economically to
First Nations people in British Columbia and Native American tribes in Alaska, northern
California, and the Pacific Northwest. Many ethnographers and historians have stressed the
cultural and nutritional importance of eulachon to the Tlingit of Southeast Alaska (Gustafson et
al. 2010). Historically, Native tribes harvested eulachon for oil and food (Spangler et al. 2003).
Fish and rendered oil were bartered with inland tribes, forming the “grease trails” of southeast
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Alaska and British Columbia (Hart 1973; ADF&G 2008; Hay et al. 1997). Eulachon currently
support important subsistence and personal use fisheries in Alaska (ADF&G 2008; Betts 1994).
Both subsistence and personal use fishing are allowed for eulachon in Cook Inlet. Eulachon
personal use fisheries take place in salt water from April 1 through May 31, and in freshwater
from April 1 through June 15. Eulachon may be harvested in the Upper Cook Inlet only by dip
net (Rodrigues et al. 2006). Most subsistence and personal use harvest in the Upper Cook Inlet
area occurs in the Twentymile River or in the estuary of Turnagain Arm.
Records from personal use and subsistence fisheries for eulachon are limited. Personal use
harvest in Upper Cook Inlet ranged from 40,377 to 89,560 fish (2.2 to 5.0 tons) from 1993
through 2003 (Shields 2004). Historically, harvest averaged approximately 4 tons in the
Twentymile River (Spangler et al. 2003). Actual personal use may be under-reported because of
confusion with subsistence harvest (Shields 2004).
5.2. Commercial Fishery
Prior to 2005, the only documented commercial harvest of eulachon in the Upper Cook Inlet area
occurred in 1978, 1980, 1998, and 1999. Gill nets were used prior to 1999, when reinterpretation
of the harvest regulation allowed use of dip nets. With the change in gear, harvest increased from
18,900 pounds in 1998 to 100,000 pounds in 1999 (Table 5.2-1).
The commercial fishery was closed from 2000 to 2005, but was reinstituted beginning with the
2006 season. The fishery is conducted under the Cook Inlet Smelt Fishery Management Plan
(Shields and Dupuis 2012), and is allowed in salt water only from May 1 through June 30, in the
area of the Cook Inlet from the Chuitna River to the Little Susitna River. Legal gear is limited to
hand-operated dip nets, with a maximum total harvest of 100 tons.
Eulachon harvest is generally limited by market demand and logistics of getting the catch to
market (Shields and Dupuis 2012). The fishery quota was reached in 2011 for the first time since
1999 (Table 5.2-1). Most of the harvest is shipped to the west coast of the United States. The
majority is sold as bait, with smaller amounts marketed for human consumption.
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Table 5.2-1. Commercial harvest of eulachon in the Upper Cook Inlet, 1978–2011
Year Gear allowed Harvest (lbs)
1978 Gill nets 300
1980 Gill nets 4,000
1998 Gill nets 18,610
1999 Dip nets 100,000
2006 Dip nets 90,783
2007 Dip nets 125,044
2008 Dip nets 127,365
2009 Dip nets 78,258
2010 Dip nets 126,135
2011 Dip nets 201,570
5.3. Sport Fishery
The Upper Cook Inlet area and the Susitna River are open to sport fisheries for eulachon.
Records prior to 1996 are limited, and many records combine eulachon and capelin Mallotus
villosus as smelt. Most of the Susitna River sport fishery occurs between RM 10 and RM 30
(ADF&G 1983b). In 1982, an estimated 3,000 to 5,000 eulachon were harvested in the Susitna
River sport fishery, but harvest decreased to between 500 and 2,000 eulachon in 1983 (Barrett et
al. 1984).
Annual sport harvest in Southcentral Alaska from 2001 through 2010 averaged approximately
57,000 smelt (eulachon and capelin combined), ranging from approximately 17,000 to 94,000
fish. Harvest in the Susitna River during this period averaged about 4,500 smelt, ranging from 0
to more than 12,500 (ADF&G 2012; Table 5.3-1).
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Table 5.3-1. Sport harvest of smelt (number of eulachon and capelin combined) in Southcentral Alaska, including Upper Cook Inlet and the Susitna River, 2001–2010
Area Year
2001 2002 2003 2004 2005 2006 2007 2008 2009 2010
Knik Arm 1,574 0 1578 11 0 71 124 0 0 0
Anchorage 35,909 57,079 35,841 9,987 8,885 9,927 16,527 20,047 28,953 34,724
Susitna River drainage 10,056 3,298 5465 12,562 3,068 0 620 1,832 3,520 4,643
West Cook Inlet drainages 0 0 455 0 0 0 0 0 880 0
Kenai Peninsula (freshwater) 23,023 20,036 12,145 41,085 9,206 3,121 3,221 2,270 4,796 6,536
Cook Inlet (saltwater) 432 373 436 2,246 1,102 2,076 1,889 277 1,136 399
Total Cook Inlet Area Sport Fish Harvest by Year 70,994 80,786 55,920 65,891 22,261 15,195 22,381 24,426 39,258 46,302
Average of Cook Inlet Area Sport Fish Harvest by
Year 11,832 13,464 9,320 10,982 3,710 2,533 3,730 4,071 6,548 7,717
North Gulf Coast/Prince William Sound 4,981 10,381 2,744 1,462 156 40 269 2305 15 39,425
Kodiak 45 0 0 0 98 0 0 0 0 178
Alaska Peninsula-Aleutian Islands 2,940 3,227 8,746 842 2,488 1,653 3,336 4,496 9,254 324
Kvichak River drainage 0 0 0 0 0 0 0 0 0 0
Nushagak, Wood River, and Togiak 1,124 40 3,309 135 2,178 175 434 859 10,038 8,078
Source: ADF&G 2012b
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5.4. Biological Importance
The high lipid content of eulachon (up to 21 percent) makes them an important prey species in
the natural environment (Payne et al. 1999). Predators include a variety of fish (e.g., spiny
dogfish shark [Squalus acanthias], Pacific salmon, Pacific halibut [Hippoglossus stenolepis],
Pacific cod [Gadus macrocephalus]), birds (e.g., cormorants, gulls, eagles), marine mammals
(e.g., beluga whales, killer whales [Orcinus orca], and harbor seals [Phoca vitulina]), brown
bears (Ursus arctos), and wolves (Scott and Crossman 1973; Willson et al. 2006). In Cook Inlet,
CIBWs and harbor seals (Phoca vitulina) are the most frequently documented eulachon predators
(NMFS 2008; Willson et al. 2006).
Harbor seals in Alaska are not classified as strategic or depleted stocks and are not listed under
the Endangered Species Act (ESA; Allen and Angliss 2011). The most recent population
estimate for the Cook Inlet/Shelikof Strait harbor seal stock is 22,900 (Allen and Angliss 2011).
Harbor seals are distributed throughout Cook Inlet, with the highest concentrations being in
lower Cook Inlet. However, sightings of harbor seals in the upper inlet have been increasing over
the past few years. The most recent aerial survey documented approximately 1,750 harbor seals
in the Susitna River delta (Shelden et al. 2011).
CIBWs reside in Cook Inlet year-round and have been documented spending significant portions
of time in Upper Cook Inlet (Funk et al. 2005; NMFS 2008; Allen and Angliss 2011). The CIBW
was listed as a federally protected endangered species under the ESA in October 2008 (73 FR
62919). The current CIBW abundance estimate is 284 whales (Hobbs et al. 2011). In April 2011,
the NMFS published a final rule designating critical habitat for the CIBW (76 FR 20180). The
NMFS identified five primary constituent elements essential to the conservation of CIBWs, one
of which was the availability of prey species, including eulachon. CIBWs use the Susitna River
delta throughout the majority of the open water season (late April through September); therefore,
occurrence in spring coincides with spawning migrations of eulachon and Pacific salmon (NMFS
2008).
6. NEED FOR ADDITIONAL DATA
Given the importance of eulachon to CIBWs and to personal use and commercial fisheries, the
historic information on eulachon needs to be updated and expanded upon from the 1980s studies
in the Susitna River. Information on timing and duration of the eulachon migration, location and
number of spawning sites, spawning site characteristics, and population characteristics are
needed to gain a comprehensive understanding of eulachon in the Susitna River, and serve as a
baseline to evaluate the potential impacts of future actions. Changes in eulachon run timing and
duration, or changes in abundance could change the availability of eulachon to CIBWs, and
effect CIBW foraging success. Limited data from the Upper Cook Inlet Eulachon Commercial
Fishery indicate that the eulachon may actually be older and larger than in the 1980s (Shields and
Dupuis 2012). Therefore, collection of age, length, and weight data is needed to establish
baseline information on population characteristics. Genetic samples would provide a baseline to
assist in determining eulachon stock structure in Cook Inlet.
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and instream flow. Chapter 5: Eulachon spawning habitat in the Lower Susitna River.
WDFW and ODFW (Washington Department of Fish and Wildlife and Oregon Department of
Fish and Wildlife). 2001. Washington and Oregon eulachon management plan. Olympia:
Washington Department of Fish and Wildlife.
Willson, M. F., R. H. Armstrong, M. C. Hermans, and K. Koski. 2006. Eulachon: A review of
biology and an annotated bibliography. National Marine Fisheries Service, Alaska
Fisheries Science Center. AFSC Processed Report 2006-12.
EULACHON WHITE PAPER
Susitna-Watana Hydroelectric Project Alaska Energy Authority
FERC Project No. 14241 March 2013
APPENDIX A. FIGURES
EULACHON WHITE PAPER
Susitna-Watana Hydroelectric Project Alaska Energy Authority
FERC Project No. 14241 Appendix A - Page 1 March 2013
EULACHON WHITE PAPER
Susitna-Watana Hydroelectric Project Alaska Energy Authority
FERC Project No. 14241 Appendix A - Page 2 March 2013
EULACHON WHITE PAPER
Susitna-Watana Hydroelectric Project Alaska Energy Authority
FERC Project No. 14241 March 2013
APPENDIX B. SPAWNING HABITAT CHARACTERISTICS
EULACHON WHITE PAPER
Susitna-Watana Hydroelectric Project Alaska Energy Authority
FERC Project No. 14241 Appendix B - Page 1 March 2013
Table B-1 Spawning habitat characteristics in the Susitna River collected during 1983a
Date RM
Water
Depth
(cm)
Water Velocity
(ft/s) Substrate Type General Habitat
Notes
5/15 12.5 130 1.0 100% silty sand Cutbank
5/15 13.8 140 1.5 100% silty sand
5/17 23.0 170 2.0 75% gravel, 25% sand
5/20 9.8 100 1.5 100% silty sand
5/20 12.5 130 1.0 100% silty sand Cutbank
5/20 18.2 100 1.0 90% sand, 10% gravel
5/21 15.0 130 1.5 60% sand, 40% gravel
5/21 25.5 120 2.0 100% silty sand Cutbank
5/22 25.5 120 2.0 100% silty sand Cutbank
5/22 27.1 130 1.5 100% silty sand Cutbank
5/22 27.3 110 1.0 100% silty sand Cutbank
5/22 27.7 150 - 100% silty sand Back eddy, cutbank
5/23 9.0 110 1.0 100% silty sand
5/23 9.7 100 0.5 100% sand and gravel mix Cutbank
5/23 21.4 160 1.0 100% silty sand Beach
5/23 22.1 - - -
5/23 23.0 170 2.0 75% gravel, 25% sand
5/24 12.5 - - 100% silty sand Cutbank
5/24 13.1 80 2.0 100% silty sand Cutbank
5/24 13.3 110 1.5 100% silty sand Cutbank
5/24 13.4 120 1.5 100% silty sand
5/24 13.8 - - 100% sand
5/24 13.8 130 1.0 100% silt Gradual slope
5/24 14.7 40 3.0 100% sand and gravel mix Gradual slope
5/24 14.9 - - 100% silty sand
5/24 15.0 - - 100% sand and gravel mix
5/24 15.5 120 2.0 100% silty sand Cutbank
5/24 15.5 130 3.0 100% silty sand Cutbank
5/24 15.7 100 - 100% silty sand Back eddy
5/24 16.2 - - 100% silty sand Beach
5/24 16.5 130 1.0 100% silty sand
EULACHON WHITE PAPER
Susitna-Watana Hydroelectric Project Alaska Energy Authority
FERC Project No. 14241 Appendix B - Page 2 March 2013
Date RM
Water
Depth
(cm)
Water Velocity
(ft/s) Substrate Type General Habitat
Notes
5/24 17.1 130 - 100% silty sand
5/24 17.2 100 1.5 100% silty sand
5/24 17.7 150 2.0 100% silty sand
5/24 18.2 100 1.0 90% sand, 10% gravel
5/24 18.7 130 1.0 75% gravel, 25% sand
5/24 19.3 140 - 100% silty sand Back eddy
5/24 19.8 100 3.0 100% silty sand Cutbank
5/24 19.8 80 1.5 100% silty sand
5/24 21.3 80 2.0 100% silty sand
5/24 22.5 120 4.0 100% silt Cutbank
5/24 23.7 100 - 100% sand Back eddy, cutbank
5/24 24.8 90 1.5 50% sand, 50% gravel
5/25 6.1 - - 100% silty sand
5/25 9.0 120 1.0 -
5/25 9.8 - - 100% silt and gravel mix
5/25 11.7 90 2.0 100% silt and gravel mix Cutbank
5/25 14.3 150 2.5 100% silty sand Cutbank
5/25 17.1 - - 100% silty sand Cutbank
5/25 19.0 140 3.0 100% silty sand Gradual slope
5/25 22.0 80 2.0 100% sand Gradual slope
5/25 24.3 90 1.5 100% silty sand Gradual slope
5/25 27.8 70 1.5 100% silty sand
5/25 29.6 70 1.5 100% silty sand Gradual slope
5/25 32.0 100 2.0 100% silty sand
5/25 34.0 80 - 98% silty sand, 2% organics Back eddy
5/25 36.0 70 1.5 100% silt and gravel mix
5/25 38.2 70 1.5 50% sand, 50% gravel
5/25 41.6 80 3.5 100% silty sand
5/25 44.0 70 3.5 50% sand, 50% gravel
5/25 44.9 80 2.0 50% sand, 50% gravel
5/25 47.0 60 1.5 50% sand, 50% gravel
5/25 49.2 40 2.0 50% sand, 50% gravel
EULACHON WHITE PAPER
Susitna-Watana Hydroelectric Project Alaska Energy Authority
FERC Project No. 14241 Appendix B - Page 3 March 2013
Date RM
Water
Depth
(cm)
Water Velocity
(ft/s) Substrate Type General Habitat
Notes
5/26 4.5 - - 100% silty sand Gradual slope
5/26 12.0 80 1.5 100% silty sand Gradual slope
5/26 25.5 - - 100% sand and gravel mix
5/27 41.5 90 3.5 100% silty sand
5/27 41.7 110 1.5 100% sand and gravel mix Cutbank
5/27 50.5 90 0.5 100% silty sand
5/28 26.2 - - -
5/29 27.5 - - 100% silty sand
5/30 25.5 - - 100% silty sand Cutbank
5/31 4.5 - - 100% silty sand Gradual slope
5/31 6.4 - - 100% silty sand
5/31 12.5 - - 100% silty sand Cutbank
a Table adapted from Vincent-Lang and Queral 1984.
EULACHON WHITE PAPER
Susitna-Watana Hydroelectric Project Alaska Energy Authority
FERC Project No. 14241 Appendix B - Page 4 March 2013
Table B-2 Water quality variables collected at selected eulachon spawning habitats in 1983a
Site RM Date Water
Temperature (°C) pH
Specific
Conductance
(µmhos)
Dissolved
Oxygen
(mg/l)
Mainstem
Discharge
(cfs)
1 20.0 5/23/83 8.1 6.6 95 10.3 66,000
2 12.8 5/24/83 6.5 6.8 93 6.4 62,000
3 13.8 5/24/83 6.7 6.9 93 8.1 64,000
4 15.0 5/24/83 6.5 6.9 93 8.6 64,000
5 15.0 5/24/83 7.5 6.8 94 8.7 64,000
6 16.2 5/24/83 7.8 6.9 94 8.3 64,000
7 18.1 5/24/83 7.2 6.9 94 7.3 64,000
8 19.5 5/24/83 8.6 6.9 96 6.1 64,000
9 21.5 5/24/83 9.3 6.9 99 6.1 64,000
10 23.0 5/24/83 8.1 6.8 95 8.9 64,000
11 20.5 5/25/83 10.8 7.2 98 10.6 62,000
12 22.8 5/25/83 9.3 7.0 99 10.3 62,000
13 23.1 5/25/83 7.8 7.0 95 10.3 62,000
14 24.9 5/25/83 9.8 7.0 101 9.4 62,000
15 26.2 5/25/83 8.0 6.7 102 5.9 62,000
16 26.5 5/25/83 9.5 6.8 102 6.5 62,000
17 28.0 5/26/83 8.6 7.2 103 11.3 64,000
18 30.1 5/26/83 8.6 7.2 103 10.8 64,000
19 33.4 5/26/83 9.1 6.8 108 6.2 64,000
20 36.5 5/26/83 8.8 7.1 103 10.1 64,000
aTable adapted from Barrett et al. 1984.