Endangered and Threatened Wildlife and Plants:

Federal Register: October 7, 2010 (Volume 75, Number 194)

Proposed Rules

Page 62070-62095

From the Federal Register Online via GPO Access [wais.access.gpo.gov]

DOCID:fr07oc10-27

DEPARTMENT OF THE INTERIOR

Fish and Wildlife Service 50 CFR Part 17

Docket No. FWS-R8-ES-2010-0013

MO 92210-0-0008-B2

Endangered and Threatened Wildlife and Plants; 12-month Finding on a Petition to list the Sacramento Splittail as Endangered or

Threatened

AGENCY: Fish and Wildlife Service, Interior.

ACTION: Notice of 12-month petition finding.

SUMMARY: We, the U.S. Fish and Wildlife Service, announce a 12-month finding on a petition to list the Sacramento splittail (Pogonichthys macrolepidotus) as endangered or threatened under the Endangered

Species Act of 1973, as amended. After review of all available scientific and commercial information, we find that listing the

Sacramento splittail is not warranted at this time. However, we ask the public to submit to us any new information that becomes available concerning the threats to the Sacramento splittail or its habitat at any time.

DATES: The finding announced in this document was made on October 7, 2010.

ADDRESSES: This finding is available on the Internet at http:// www.regulations.gov at Docket Number FWS-R8-ES-2010-0013. Supporting documentation we used in preparing this finding is available for public inspection, by appointment, during normal business hours at the U.S.

Fish and Wildlife Service, San Francisco Bay Delta Fish and Wildlife

Office, 650 Capitol Mall, Sacramento, CA 95814. Please submit any new information, materials, comments, or questions concerning this finding to the above street address.

FOR FURTHER INFORMATION CONTACT: Dan Castelberry, San Francisco Bay

Delta Fish and Wildlife Office (see ADDRESSES); by telephone at 916- 930-5632; or by facsimile at 916-930-5654. If you use a telecommunications device for the deaf (TDD), please call the Federal

Information Relay Service (FIRS) at 800-877-8339.

SUPPLEMENTARY INFORMATION:

Background

Section 4(b)(3)(B) of the Endangered Species Act of 1973, as amended (Act) (16 U.S.C. 1531 et seq.), requires that, for any petition to revise the Federal Lists of Endangered and Threatened

Page 62071

Wildlife and Plants that contains substantial scientific or commercial information that listing the species may be warranted, we make a finding within 12 months of the date of receipt of the petition. In this finding, we will determine that the petitioned action is: (1) Not warranted, (2) warranted, or (3) warranted, but the immediate proposal of a regulation implementing the petitioned action is precluded by other pending proposals to determine whether species are tendangered or threatened, and expeditious progress is being made to add or remove qualified species from the Federal Lists of Endangered and Threatened

Wildlife and Plants. Section 4(b)(3)(C) of the Act requires that we treat a petition for which the requested action is found to be warranted but precluded as though resubmitted on the date of such finding, that is, requiring a subsequent finding to be made within 12 months. We must publish these 12-month findings in the Federal

Register.

Previous Federal Actions

Please refer to the final listing rule (64 FR 5963) for a discussion of Federal actions that occurred prior to February 8, 1999.

Please refer to the Notice of Remanded Determination of Status for the

Sacramento Splittail (68 FR 55139) for a discussion of Federal actions that occurred after February 8, 1999, and prior to September 22, 2003.

It is our intent, in this document, to reiterate and discuss only those topics directly relevant to this decision.

On September 22, 2003, the Service published a Notice of Remanded

Determination of Status for the Sacramento Splittail in the Federal

Register (68 FR 55139) that removed the Sacramento splittail from the

List of Endangered and Threatened Wildlife (50 CFR 17.11(h)). On August 13, 2009, the Center for Biological Diversity (CBD) filed a complaint in U.S. District Court for the Northern District of California, challenging the Service on the merits of the 2003 determination alleging improper political influence. In a settlement dated February 1, 2010 (Case4:09-cv-03711-PJH), the Service agreed to open a 30-day public comment period for a new 12 month finding to allow for the submission of additional information by the public. The Service also agreed to submit to the Federal Register a new status review and 12- month finding as to whether listing the Sacramento splittail is warranted or not warranted. If warranted, the Service further agreed to publish, concurrently with the 12-month finding, a proposed rule to list the Sacramento splittail before September 30, 2010 and a final determination on or before September 29, 2011.

Definitions

To assist the reader in understanding terminology used in this determination, we have provided below several terms with their corresponding definitions as they are used in this document. As used in this determination, the term ``Delta'`` refers to all tidal waters contained within the legal definition of the San Francisco Bay-

Sacramento-San Joaquin River Delta, as delineated by section 12220 of the State of California's Water Code. Generally, the Delta is contained within a triangular area that extends south from the City of Sacramento to the confluence of the Stanislaus and San Joaquin Rivers at the southeast corner and Chipps Island in Suisun Bay at the southwest corner. The term ``Estuary'' as used in this determination, refers to the collective tidal waters contained in the Sacramento and San Joaquin

Rivers, the Delta, and San Pablo and San Francisco bays.

Species Information

Species Description

The Sacramento splittail is a fish species native to central

California and represents the only extant species in its genus in the world (Baerwald et al. 2007, p. 160). Splittail can grow to a length of 40centimeters (cm) (15 inches (in.)), and have an elongate body, small head, and enlarged upper tail lobe. Their body coloration is dusky olive gray on the back and silver on the sides. During breeding season, their fins become tinged with red-orange. Additionally, males develop white tubercles on their heads and become darker in color during the breeding season (Moyle 2002, p. 146).

Taxonomy

Splittail were first described in 1854 by W.O. Ayres as Leuciscus macrolepidotus and by S.F. Baird and C. Girard as Pogonichthys inaeqilobus. Although Ayres' species description is accepted, the species was assigned to the genus Pogonichthys in recognition of the distinctive characteristics exhibited by the two splittail species P. ciscoides and P. macrolepidotus (Hopkirk 1973, p. 24). Pogonichthys ciscoides, endemic to Clear Lake, Lake County, California, has been extinct since the early 1970s. The Sacramento splittail is currently classified as Pogonichthys macrolepidotus. Recent studies have revealed two populations of splittail that differ in their genetic makeup, one in the Napa/Petaluma drainages (hereafter referred to as the San Pablo population) and one in the greater Central Valley drainage (hereafter referred to as the Delta population) (Baerwald et al.2007, pp. 159- 167).

Distribution

Historically, Sacramento splittail were found as far north as

Redding on the Sacramento River. Splittail were also found in the tributaries of the Sacramento River as far as the current Oroville Dam site on the Feather River and Folsom Dam site on the American River

(Rutter et al. 1908, p. 131). Along the San Joaquin River, splittail were harvested by native peoples in Tulare and Buena Vista Lakes where splittail bones have been found in archeological middens (Moyle et al., 2004, p. 7). In the San Francisco Bay area, splittail have historically been reported at the mouth of Coyote Creek in Santa Clara County and the Southern San Francisco Bay (Snyder et al. 1905, pp. 327-338).

Splittail were documented in Suisun and Napa marshes as well as Suisun

Bay in the 1950's (Caywood . 1974, p. 29-65).

Splittail occur in the San Francisco estuary and its tributaries and are found most often in slow moving sections of rivers and sloughs including dead end sloughs and shallow edge habitats (Moyle 2002, p. 147; Daniels and Moyle 1983, p. 653; Feyrer et al. 2005, pp. 164-165).

Recent studies have shown the splittail's range in the Sacramento, San

Joaquin, Napa, Mokelumne and Petaluma rivers is significantly greater than previously thought when it was first petitioned in the early 1990's as a threatened species (Sommer et al. 2007, pp. 27-28; Sommer et al. 1997, p. 970). The following chart created by Sommer and featured in his splittail paper follows (Sommer et al. 2007, p. 28).

Page 62072

Table 1. Upstream-most locations of historical and recent splittail collections (1998-2002). River kilometer (rkm) is the distance from the mouth of the river. Location (rkm) of splittail collection

Recent (Freyer et al.

River System

Historic (Rutter 1908) 1970s (Cawood 1974) Mid- 1990s (Sommer et

05) unless noted

Distance to first al. 1997)

otherwise

dam\a\

Sacramento

483

387

331

391\b\

387

Feather

109

Present

94

94\c\

109

American

49

37

19

No new data

37

San Joaquin

Widespread

Present

201

218.5\d\

295

Mokelumne

NA

25

63

96\e\

63

Napa

NA

21

10

32

NA

Petaluma

NA

25

8

28

NA

\a\ Lowest dams in reach of river are Red Bluff (Sacramento), Oroville (Feather), Nimbus (American), Sack (San Joaquin), and Woodbridge (Mokelumne).

Woodbridge is a seasonal dam. Napa River is not dammed within the range of splittail; first dam was removed from the Petaluma River in 1994.

\b\ D. Killam, California Department of Fish and Game, personal communication.

\c\ B. Oppenheim, NOAA Fisheries, personal communication.

\d\ R. Baxter, California Department of Fish and Game, unpublished data.

\e\ J. Merz, East Bay Municipal Utility District, November 2000.

Distribution on the Sacramento River over the past 30 years has consistently ranged at least 232 to296 river kilometers (rkm) (144 to184 miles (mi)) upstream of the estuary (Feyrer et. al. 2005, pp. 163-167). The consistent finding of splittail more than 200 rkm (124 mi) upstream of the Estuary may represent a population persisting there or may reflect the long distance that splittail migrate during dry years (Feyrer et al. 2005, pp. 165-166). Juvenile splittail have been recorded at the Glenn-Colusa Irrigation District Intake at rkm 331 (206 mi) on the Sacramento River year-round from 1994 - 2001. It is unknown why these individuals do not migrate downstream after spawning as do the majority of splittail (Feyrer et al. 2005, pp 165-166). Splittail have been documented on the Toulumne River to rkm 27.4 (mi 17) (Heyne 2003, pers. comm.) and on the Merced River to rkm 20.9 (13 mi) ( Heyne 2003, pers. comm.). Splittail have been recorded in recent times from within Salt Slough (Baxter 1999a, p. 10; 1999b, p. 30). A 1998

California Department of Fish and Game (CDFG) gillnet survey of the tidal reaches of the Lower Walnut Creek found splittail to be the most abundant fish in the creek (Leidy et al. 2007). Splittail are found in the Napa Marsh during years with high freshwater flow, but are rare during years of low freshwater outflow (Baxter 1999a, p. 11).

Splittail can utilize a variety of habitats and having no known collection in an area does not mean that splittail are not there because it is impractical to survey the entire Delta. Splittail have been observed in a number of tributaries of major rivers such as the

Sacramento and San Joaquin and are likely distributed much more widely in small creeks and marshes throughout the lower portions of the

Estuary than known collections indicate (Kratville 2010, pers comm.).

Suisun Marsh and Bay contain the largest areal extent of shallow water habitat available to the splittail and likely have the greatest concentrations of the species.

Splittail's spawning habitat includes the natural and newly- restored floodplains of the Cosumnes River, managed floodplains such as the Yolo and Sutter bypasses, and disjunct segments of floodplain adjacent to the Sacramento and San Joaquin rivers and tributaries.

These areas approximate the large, open, shallow-water areas which once existed throughout the Delta (Sommer et al. 1997, p. 971). The largest portion of splittail spawning habitat occurs in the Yolo Bypass and higher splittail young-of-the-year abundances are strongly correlated with the flooding of the Yolo Bypass. The best spawning conditions for splittail occur in the bypass when water remains in the bypass until fish have completed spawning (at least 30 days), and larvae are able to swim out on their own during the draining process.

In years where the Yolo and Sutter bypasses are not inundated for at least 30 days, splittail spawning is confined primarily to the natural and newly restored floodplains of the Cosumnes River and the margins of rivers and other floodplain features that are inundated at lower river stages. The Cosumnes River is unique in that it is the only major river flowing into the Delta that does not host a major dam.

There are indications, based on presence of larvae and juveniles, that spawning in the Sacramento River occurs relatively far upstream at

Colusa (Baxter 1999a, p. 8; 1999b, p. 29). Splittail also utilize the

San Joaquin River for spawning in wet years when river flow exceeds the capacity for storage and flooding occurs. The Tuolumne, Cosumnes,

Feather, American, Napa, and Petaluma Rivers, and numerous other smaller waters also support splittail spawning activity.

In summary, the geographic distribution of the splittail has not decreased detectably over the last several decades and is in fact larger than estimated in our last listing decision (Sommer et al. 2007, pp.27-28; 68 FR 55139).

Habitat Requirements

Although primarily a freshwater species, splittail tolerate salinities as high as 10 to 18 parts per thousand (ppt) (Moyle and

Yoshiyama 1992). Salinity tolerance in splittail increases in proportion to body length; adults can tolerate salinities as high as 29 ppt for short periods in laboratory conditions, but experience loss of equilibrium (bodily balance) when salinities exceed 23 ppt (Young and

Cech 1996, p. 668). Hospitable temperatures for non-breeding splittail range from 5 to 24[deg] Celsius (C) (75[deg] Fahrenheit (F)) although acclimated fish can survive temperatures up to 33[deg]C (91[deg] F) for short periods of time (Young and Cech 1996, pp. 667-675). Splittail are also tolerant

Page 62073

of low dissolved oxygen and can be found in water where levels are around 1 mg O\2\ L -\1\ (Moyle et al. 2004, p. 13).

Splittail are frequently found in areas subject to flooding because they require flooded vegetation for spawning and rearing. Historically, the major flood basins (e.g., Colusa, Sutter, American, and Yolo basins; Tulare, Buena Vista, and Kern lakes) distributed throughout the

Sacramento and San Joaquin valleys provided spawning and rearing habitat. These flood basins have all been reclaimed or modified for flood control purposes (i.e. as bypasses), and much of the floodplain area adjacent to the rivers is now inaccessible behind levees.

Splittail make use of the Sutter Bypass, and particularly heavy use of the Yolo Bypass, for spawning under certain hydrologic conditions.

The shallow, vegetated waters of the bypasses provide excellent rearing conditions for juvenile fish (Sommer et al. 2001, p. 11). The bypasses are primarily flood control facilities and secondarily, passively operated as agricultural lands. These lands are also managed for waterfowl and other wildlife habitat. Splittail using the bypasses are subject to the same threats found elsewhere, such as habitat loss, environmental contamination, harmful reservoir operations, competition with and predation by non-native fish, and so forth.

The bypasses are only fully flooded when flows in the Sacramento

River reach a certain level. The Yolo Bypass becomes inundated when the

Sacramento River flow rate at the Freemont Weir exceeds 1,600 cubic meters per second (cms) (56,503 cubic feet per second (cfs)). This occurs when the River reaches approximately 9.0 meters (m) (30 feet

(ft.) (National Geodetic Vertical Datum standard) in depth at the

Freemont Weir (Sommer et al. 2001, pp. 7-8). Partial flooding of the

Yolo Bypass via high flows from Cache and Putah creeks can occur independently regardless of Sacramento River flows. Due to the unpredictable flooding frequencies and duration of the bypass, splittail, having migrated long distances upstream, could arrive at floodplains that have not been inundated and therefore the splittail could be denied the opportunity to spawn. In those cases where adult splittail successfully spawn, the eggs or larvae could become trapped and killed if waters recede too rapidly. Insufficient duration of floodplain inundation could also force egress of juvenile splittail before they have attained a size and swimming ability sufficient to avoid predation. The annual splittail spawning and reproductive success is strongly correlated with frequency and duration of Yolo bypass inundation (Sommer et al. 2007, pp. 33-34).

The Fremont Weir has been overtopped--resulting in Yolo Bypass inundation--19 of the last 31 years with 10 of these years producing inundation durations of more than 30 days (DWR 2010a, pp. 1-2).

Inundation durations of 30-90 days are needed to produce robust splittail year classes on the bypass (Kratville 2010, pers. comm.).

According to the ST5 (T. C. Foin) model, the inundation of floodplains that splittail utilize as spawning habitat must occur at a minimum of every 7 years for a minimum of 30 days for splittail populations to persist. Bypasses and other floodplains have historically been exceeding these parameters and we have no evidence that suggests they will not continue to do so in the foreseeable future.

The Yolo Bypass supports agricultural crops such as corn and safflower and can support tomatoes in non-flood years. Optimal flooding conditions for the splittail (February through May) have negative effects on agricultural production in the area destroying and damaging crops, eroding soils and decreasing overall yields (Yolo Bypass

Management Strategy 2001, ch. 2 p. 6). Because Yolo Bypass inundation is likely to be one of the most important factors in determining the continued production of high splittail population numbers, cooperation on the flood management between the landowners of the bypass and resource management agencies is essential.

Splittail spawning occurs over flooded vegetation in freshwater marshes, sloughs, and shallow reaches of large rivers with depths of at least 1m (3.3 ft) (Moyle et al. 2007 , pp. 1-27). Observations of splittail spawning have indicated the species spawns at depths of less than 1.5 m (4.9 ft) in the Cosumnes River floodplain and at depths of less than 2 m (6.6 ft) in Sutter Bypass (Moyle et al. 2004, pp. 16-17).

These studies show that splittail spawn in water depths between 1 to 2 m (3.3 to 6.6 ft) depending on location of spawning. Splittail may not spawn again in the year following a successful effort (Moyle et. al. 2004, p. 32).

It is speculated that Suisun Marsh is the late-stage rearing area for juvenile splittail hatched and reared in the extensive spawning habitat found within the Yolo Bypass because water flowing out of the

Yolo Bypass tends to stay on the north side of the delta and be drawn into Suisun Marsh (Moyle et al. 2004, p. 31).

Biology

Splittail are relatively long-lived and larger fish may be 8 to 10 years old (Moyle 2002). Splittail reach about 110 millimeters (mm) (4.3 in) standard length (SL) (tip of the snout to the posterior end of the last vertebra)in their first year, 170 mm (6.6 in) SL in their second year, and 215 mm (8.4 in) SL in their third year (Moyle 2002, p. 148).

Male and female splittail generally mature by the end of their second year, but some males mature in their first year and some females do not mature until their third year (Daniels and Moyle 1983, p.650).

Estimates of splittail fecundity have shown high variability in numbers of eggs produced. Caywood (1974, p. 4015) found a mean of 165 eggs per mm of SL of fish sampled and reported a maximum of 100,800 eggs in one female. Feyrer and Baxter (1998, p. 123) found a mean of 261 eggs per mm of SL and a fecundity range of 28,416 to 168,196 eggs.

Bailey et al. (1999) examined fish held for a considerable time in captivity and found that fecundity ranged from 24,753 to 72,314 eggs per female, which most closely agrees with Caywood's (1974, p. 4015) observations.

Splittail are benthic (feeding in the bottom of the water column) foragers that mainly feed in the daytime. Composition of splittail gut contents has revealed that they feed almost exclusively on aquatic invertebrates with chironomid larvae making up the largest portion of the diet in all areas except the Petaluma River where copepods make up the largest portion of the diet (Feyrer et al. 2007a, p. 1398). Until the 1980's, opossum or mysid shrimp (Neomysis mercedis), made up a large portion of the diet along with amphipods and harpacticoid copepods (Moyle et al. 2004, p. 14). Introductions of the Asiatic clam

(Corbicula fluminea) in 1945 and more importantly the overbite clam

(Corbula amurensis) first recorded from the estuary in 1986) were followed by a sharp decline in shrimp abundance that started in 1987 and continued through 1999 (Feyrer et al. 2003, p. 283). Splittail have shifted their diet from prey items such as mysid shrimp to a diet increasingly focused on bi-valves, in particular the overbite clam.

Opossum shrimp in splittail gut contents were reduced from 24 percent

(historically) to 2 percent by 2003 (Feyrer et al. 2003, pp. 277-288;

Kratville 2010, pers comm.). In the Estuary, clams, crustaceans, insect larvae, and other invertebrates also are found in the adult diet.

Larvae feed mainly on plankton composed of small

Page 62074

animals (zooplankton), moving to small crustaceans and insect larvae as body size increases (Kurth and Nobriga 2001, EIP newsletter vol. 14, num.3, p. 41).

Splittail populations fluctuate annually, depending on spawning success, which is positively well-correlated with freshwater outflow and the availability of shallow water habitat with submerged vegetation

(Daniels and Moyle 1983; Sommer et al. 1997). Sexual maturity is typically reached by the end of their second year. Splittail are a migratory species that travel upstream into freshwater floodplain habitat to spawn. The onset of spawning is associated with rising water levels, increasing water temperatures, and increasing day length. Peak spawning occurs from February through May, although records of spawning exist for late January to early July (Wang 1986). One temporally stable cue for splittail is the timing of the vernal equinox (Feyrer 2006, p. 221). Peak flow from the Central Valley enters the Estuary approximately at the same time as the vernal equinox (Feyrer 2006, p. 221) and these coinciding events commence splittail migration. In some years, most spawning may take place within a limited period of time.

For instance, in 1995, a year of high spawning activity, most splittail spawned over a short period in April (Moyle et al. 2004, p. 16). Within each spawning season, older fish reproduce first, followed by younger individuals (Caywood 1974, p. 50).

Bailey (1994, p. 3) has documented that splittail eggs hatch in 3 to 5 days at 18.5[deg] C, (65.3[deg] F). Bailey (1994, p. 3) also found that at 5 to 7 days after hatching, the yolk sac is absorbed and the diet begins to include small rotifers. Splittail larvae remain in shallow, weedy areas close to spawning sites for 10 to 14 days and move into deeper water as they mature and swimming ability increases (Sommer et al. 1997, pp. 961-976). When the flood waters recede juveniles typically leave the flooded areas and move downstream in May, June, and

July to rear in estuarine marshes (Moyle et al. 2004, p. 17). Splittail can be easily identified at 20 to 25 mm (0.8 to 1.0 in) total length

(TL) and become fairly active swimmers at this time (Moyle et al. 2004, p. 17).

Abundance

History of abundance models and evaluations

An estimate of splittail abundance has never been performed; however, survey data have been used to construct indices of abundance that have been used in the past to assess population trends (Sommer et al. 2007, p 29; Moyle et al. 2004, p 7). In general, the applicability of survey data to a particular use arises from two factors: (1) How the data are collected; and (2) how the data are used to estimate or to index abundance. The key point with regard to the first factor is the degree to which the sample collected is representative of the sampled population. Gear type, configuration, and method of deployment all contribute to species, sizes, and life stages collected. Unequal vulnerability of different sizes of fish to a given sampling protocol results in systematic error in population estimation. Fish behavior, both between species and between life stages, also contributes to sampling error, as does habitat variation, because gear performance often differs among habitat types. The efficiency of open-water, or pelagic, sampling may be affected by physical factors such as flow velocity and turbidity, both in terms of gear performance and fish behavior.

Splittail are a benthic (near-bottom-dwelling) species, often occur in shallow edge habitat, and feed most actively in early morning (Moyle et al. 2004, p 8; Moyle 2002, p 148). Splittail would not be expected to be collected efficiently in surveys that do not sample channel edges and bottom habitats effectively. Further, while combining data from the various surveys provides reasonably good coverage of the geographic range of splittail, individual surveys are often fairly limited in geographic scope. All surveys suffer from selection biases due to the type of gear deployed and the method of deployment (Ricker et al. 1975, pp 70-73; 92). None of the surveys used to construct the indices used to monitor the relative abundance of splittail was designed specifically to sample splittail, and each is limited in some manner in its ability to adequately represent splittail population trends.

Therefore, the data collected do not represent a quantitative estimate of population size.

The surveys and their limitations are described in the Service's

Notice of Remanded Determination of Status for the Sacramento Splittail

(68 FR 55139). Sommer et al. (2007, pp 29-30) and Moyle et al. (2004, pp 8-13) also explain some of the important limitations of the surveys with respect to splittail. A chart summarizing the surveys and their limitations is provided below.

Table 2. Summary of splittail sampling surveys

Survey

Brief Description

Years

Pros

Cons

CDFG Fall Mid--Water Trawl

Designed to sample 1967--present

Catches all

--Targets striped juvenile striped

splittail size

bass bass.

classes

--Low adult catch 100 sampling sites:

rate

San Pablo Bay in

--Sampling does the west to Rio

not cover entire

Vista on the lower

range

Sacramento River.

--Does not sample and to Stockton on.

benthos or the San Joaquin

shallow channel

River.

edges

--Some years yield no splittail

--Splittail are better able to see nets in recent years due to decreased turbidity

San Francisco Bay Mid--Water

Samples west of the 1980--present

--Two types of

--Does not cover

Trawl and Otter Trawl Survey

Delta

sampling

entire range seaward to south

equipment and

--Non--specific;

San Francisco Bay.

frequent sampling. targets entire

--Capture all size pelagic or classes.

benthic community

--Incomplete data between 1989-- 1999

--Splittail only caught in 5 percent or less of samples

Page 62075

University of California at

Long--term study of 1979--present

Samples all size

--Non--specific;

Davis (UC Davis) Suisun Marsh the

classes

targets entire

Otter Trawl

ecology of the

fish community entire fish

--Geographically community of the

limited marsh at 21 sites

--Larger fish less and 9 sloughs.

vulnerable to trawls

Chipps Island Survey

U.S. Fish and

1976--present

--Samples well

--Designed to

Wildlife Service

during high flow sample juvenile conducts a

years

salmonids sampling program

--Good adult catch --Geographically for juvenile

rates.

limited salmon in the deep

--Samples near-- water channel near

surface waters

Chipps

only

Island, midwater

--High turbidity trawl is pulled at

in sampling area the. surface in 10 20-- minute hauls per day during May and

June.

FWS Beach Seine Survey

Samples 23 stations 1979--present

--Broadest

--Inconsistent around Delta with

geographical

from 1983--1992 15--m beach seine

coverage of all

--Focused on out-- in low velocity

surveys

migrating areas near

--Good adult

juvenile salmon shoreline

catches.

----Low adult catch

Salvage Operations

The Central Valley 1979--present

Highest number of --Geographically

Project (CVP) and

splittail caught localized--mainly

State Water

out of any survey reflective of San

Project (SWP)

for both adult

Joaquin River operate fish

and juvenile

production screening

catches

--Catches are facilities to

result of divert fish away

entrainment and from the pump

often cause intakes into

mortality holding facilities where fish are counted,. measured, and released..

Please refer to February 8, 1999, final listing rule (64 FR 5963) for a full discussion of methods used to estimate abundance in that rule. Please refer to the September 22, 2003, Notice of Remanded

Determination of Status for the Sacramento Splittail (68 FR 55139) for a full discussion of methods used to estimate abundance for that document. In our January 6, 1994, proposed rule to list the Sacramento splittail as threatened (59 FR 862), we initially evaluated and analyzed splittail survey data using a method published by Meng and

Moyle (1995, p. 541) in the Transactions of the American Fisheries

Society. Meng and Moyle used a common data set from the years 1980-1992 to compare point estimates with the Mann-Whitney U-test. We used this same method during the development of our 1999 final listing rule (64

FR 5963, February 8, 1999), using abundance data provided and updated by CDFG, California Department of Water Resources (CDWR), and UC Davis.

Using the aforementioned method, the 1999 finding concluded that the splittail had declined by 62 percent in abundance over the last 15 years.

In a document we published in the Federal Register on August 17, 2001 (66 FR 43145), we requested public comments to assist us in reanalyzing our splittail abundance data. In that document, we presented a stratified Mann-Whitney U-test, which represented an improvement on what essentially remained a Meng and Moyle (1995, pp. 538-549) statistical approach. Following careful consideration of comments we received from numerous respondents to this document, including those provided through the peer review process, we concluded that the abundance indices and Multiple Linear Regression (MLR) model jointly developed and submitted by CDFG and U.S. Bureau of Reclamation

(USBR) in 2001 (hereafter referred to as the CDFG/USBR MLR Model) provided the best scientific data (method) available for statistically evaluating temporal trends of splittail abundance information. We used this CDFG/USBR MLR Model as the basis of our September 22, 2003, Notice of Remanded Determination of Status for the Sacramento Splittail (68 FR 55139), instead of the original Meng and Moyle (1995, pp. 540-542) methodology. We input 20 discrete sets of age-specific abundance monitoring data into the model. These data sets were obtained from the surveys described in Table 2 above. Running the model in a ``worst case scenario'' (alpha 10values of 0.9 mg/kg-dw in feed, 7.9 mg/kg-dw in muscle, and 18.6 mg/kg-dw in liver for juveniles. The derived EC10values by Rigby et al. (2010, p. 79) represent the predicted selenium concentration at which deformities would be observed in 10 percent of the juvenile population.

In a laboratory setting, research by Teh et al. (2004, p. 6092) has shown that the prevalence of deformities among juvenile splittail in the laboratory increase at dietary concentrations greater than 6.6 mg/ kg-dw while concentrations of 26.0 mg/kg-dw and greater significantly decrease body weight, total length, and condition factors of juvenile splittail. This may be due to the liver's inability to metabolize and excrete biochemicals due to its reaction to high selenium intake (Teh et al. 2004, p. 6092).

In field settings, selenium concentrations analyzed from tissues of adult splittail captured in the Suisun Bay/Marsh area show elevated concentrations in muscle ranging from 4 to 5 mg/kg (5 ppm), and liver concentrations ranging as high as 20 mg/kg (20 ppm) (Stewart et al. 2000, p. 1). The median selenium liver g/g-dwconcentrations in splittail collected from Suisun Bay are about 13 (13 ppm) (Stewart et al. 2004, p. 4523). Although deformities typical of selenium exposure including lordosis (spinal deformities) have been observed in splittail collected from Suisun Bay (Stewart et al. 2004, p. 4524), the known data on muscle and liver concentrations in splittail adults are below the EC10values derived by Rigby et al. (2010, pp. 76-79).

Current threshold tolerances of selenium exposures by splittail may be higher than other species that use upper portions of the water column (Teh et al. 2004, pp. 6087-6090). However, laboratory and field studies cited above lead us to conclude that although selenium is considered elevated within the Delta, selenium exposures, although important, are not having a significant population-level effect on the species.

Bioaccumulation of selenium by splittail in the Estuary is a potential concern because the diet of adult splittail consists of bivalves (including Asiatic clam and overbite clam), amphipods, cladocerans, harpacticoid copepods, mysids, and detritus (Moyle et al. 2004, p. 22). Asiatic and overbite clams are benthic filter feeders that take up and accumulate selenium (Stewart 2004, p. 4522). The relationship between the bioaccumulation of selenium in the overbite clam and its predation by splittail may be significant because subsequent to the clam invasion, splittail shifted their diet from prey items such as estuarine copepods to a diet increasingly focused on bivalves, in particular, overbite clams (Feyrer et al. 2003, p. 285).

The recent increased reliance of splittail on overbite clams as a food source may be a risk factor for increased selenium accumulation in splittail. Concentrations of selenium in overbite clams in the San

Francisco Bay Estuary rose three fold from the mid 1980's to 1997. Some of this rise may have been a result of high run-off during the wet years of 1995-1997 (Linville 2002, p. 56-59) when the survey was concluding. In the San Francisco Bay, selenium concentrations in

Asiatic and overbite species range from 2 to 9 and 5 to 20 mg/kg-dw, respectively (Stewart et al. 2004, p. 4522; Presser and Luoma 2006, p. 48) compared with other native diet items of amphipods and mysids which range from 1 to 3 mg/kg-dw (Stewart et al. 2004, p. 4522). These concentrations exceed the previously discussed dietary EC10 of 0.9 mg/kg-dw derived by Rigby et al. (2010, p.78). However, the

EC10value developed by Rigby et al. (2010, p. 78) reflects adverse effects upon juveniles from dietary exposures. In Suisun Marsh adult splittail gut contents are predominantly detritus (Feyrer et al. 2003, p. 281). Feeding behavior of splittail in Suisum Marsh suggest they are more dependent upon detritus food sources which would likely expose them to lower concentrations compared of selenium to bivalve and amphipod diet sources.

Moyle et al. (2004, p. 17) hypothesized that success of juvenile downstream migration is strongly linked to the size that juvenile splittail achieve prior to exiting the spawning areas. It was suggested that a minimum size of 25 mm (1 in) greatly enhances success of downstream migration. Moyle presented data demonstrating statistically- significant declining growth rates. The apparent declines in growth rates observed in Suisun Marsh splittail between 1980 and 1995 by Moyle et al. (2004, p. 14) were correlated to the invasion of the Estuary by the overbite clam, and the subsequent shift of splittail to an overbite clam-dominated diet. Moyle et al. (2004, pp. 14-15) suggested that this trend might reflect cachexia (contaminant-induced weight loss despite calorically sufficient dietary intake) which is a classic symptom of non-lethal selenium poisoning. However, Moyle et al. (2004, p. 30) also suggested this decline in growth rates may reflect poorer energetics from shifting to a non-mysid shrimp-dominated diet.

Steps have been taken to reduce the input of selenium into the

Estuary (see discussion under Factor D) and selenium loads discharged from the San

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Joaquin drainage have been reduced over the last decade. In addition, the predominant source of selenium in the Delta (i.e., irrigation drainage from the San Joaquin River watershed) is somewhat removed from areas containing important spawning habitat for the species (Sacramento

River watershed). Furthermore, studies on the effects of the overbite clam on splittail abundance have been inconclusive. Feyrer et al. found that changes in the food web have had effects on the diets of older splittail (2003, pp. 278-285), but Kimmerer found no evidence that the splittail decline was directly related to the decline in opossum shrimp

(2002, pp. 51-52). Therefore, we have no conclusive scientific data finding that the splittail growth rates are the result of any selenium induced bioaccumulation mechanism. While there is scientific information that indicates overbite clams do accumulate selenium, there is no indication that the bioaccumulation of selenium in splittail as the result of eating these bivalves has resulted in a population decline of the species. Therefore, we conclude that selenium does not constitute an immediate threat to the splittail through all or a part of its range at this time or in the foreseeable future. However, the potential long-term chronic threat that selenium may present to splittail condition and health cannot be discounted when combined with other potential water quality stressors and should be examined in more detail in the future.

Mercury

The Sacramento River watershed was the site of significant mining activity during the 19th century, including hard rock and hydraulic gold mining (primarily in the Sierra Nevada), mercury mining in the

Coast Range (primarily to support gold mining), and hard rock mining for copper, silver, and other metals in portions of the Sierras and northern Coast Range. California's Coast Range represents one of the world's five major mercury mining areas (Jasinski 1995, p. 151).

Historic hydraulic gold mining and gold dredging beginning in the 1850's in mountains upstream of the Delta set in motion a continual stream of mercury flowing into the Estuary from the Sacramento watershed that is still having residual effects today (Healy 2008, p. 23).

Analytical data indicate that mercury concentrations in aquatic biota in the San Joaquin River are exceeding screening thresholds and may pose ecological and human health risks (Davis et al. 2000, pp. 9- 16). Laboratory studies by Deng et al. (2008, p. 200-202) found dietary mercury and a combination of mercury and selenium caused damage to liver, kidney and gill tissue of splittail after four weeks of exposure. Although liver glycogen depletion and kidney tubular dilation were observed by the Deng et al. study, these lesions did not seem to pose a direct threat to the survival of the splittail larvae (2008, p. 202). Because splittail require floodplain inundation to reproduce, they need habitats like the Yolo Bypass and the Cosumnes River floodplain. The reliance on these regions for reproduction creates a potential risk for eggs and juveniles to be exposed to mercury contamination. However, field studies regarding mercury toxicity to splittail eggs and juveniles are lacking.

Regarding risks from bioaccumulation of mercury via the food chain pathway, several research groups are currently addressing mercury accumulation in the Delta food web. However, no systematic study exists of mercury distributions in the food web of the Bay. Bioaccumulation processes depend on the amount of mercury in surficial sediments, the water quality at the sediment/water interface, and local food web dynamics.

Methylmercury is the most important form of mercury in the aquatic environment with regard to accumulation by biota and transfer through the food web. Methylmercury is produced through addition of a methyl group to Hg2+, a process referred to as methylation. The precise mechanism for entry of methylmercury to the food chain is unknown.

However, this initial step is critical, because concentrations of mercury in plankton can be about 10,000-fold higher than in water

(Krabbenhoft 1996, p. 2). After this initial step, methylmercury concentrations increase approximately 0.5 log units per trophic level

(Watras and Bloom 1992, p.1316), suggesting that each successive trophic level derives methyl-Hg from a progressively more concentrated source (i.e. the previous trophic level), in a process known as biomagnification. In this process consumers retain and further concentrate much of the methylmercury of their prey and subsequently pass this on to the next trophic level. Species at high trophic positions in the aquatic food web, such as predatory fish, attain concentrations that are approximately a million times higher than concentrations in water. Because methylmercury biomagnifies, trophic position is one of the primary factors influencing observed tissue concentrations.

Given that splittail are fairly low in trophic status and feeding guilds in the Estuary, the likelihood of accumulating and biomagnifying mercury from the food web is low. One study has linked elevated mercury to the Cosumnes River floodplain and the Yolo Bypass (Slotten et al. 2000, p. 44), which are both primary spawning grounds for splittail.

However, this study found no increased levels of mercury in lower trophic level biota that occurred in these floodplains (Slotten et al. 2000, p. 44). Although laboratory studies have shown mercury to have adverse effects to splittail individuals and there are increased risks of mercury exposures in splittail spawning grounds, the Slotten study did not find that these mercury levels transferred into the food web and additional field studies regarding mercury toxicity to splittail are lacking.

We have considered mercury as a possible threat to the splittail, but there is limited information on the effects of mercury on splittail population dynamics. Therefore we have determined that mercury and its potential for bioaccumulation and/or biomagnifications does not constitute a significant threat to splittail now or in the foreseeable future.

Organophosphates

Organophosphate pesticides such as diazinon, chlorpyrifos, and malathion are toxic at low concentrations to some aquatic organisms.

Several areas of the Delta, particularly the San Joaquin River and its tributaries, are listed as impaired under the Clean Water Act due to elevated levels of diazinon, chlorpyrifos, and other pesticides.

Organophoshates enter agricultural drainage mainly in stormwater runoff because it is sprayed on orchards during the rainy winter season. The environmental fate of chlorpyrifos and diazinon are not well understood. Previous work shows that chlorpyrifos is adsorbed strongly onto sediment particles, reducing the aqueous concentration (Karen et al. 1998, p.1584). The fate of adsorbed chlorpyrifos is not known. For chlorpyrifos dissolved in water, volatilization, photolysis, and hydrolysis are major removal mechanisms (Howard, 1999; Racke, 1993).

The role of biodegradation in chlorpyrifos removal is not well understood. Giddings et al. (1997) did find that the degradation of chlorpyrifos in water followed a first-order decay model (p. 2360). The environmental fate of diazinon is less known, but it is more soluble than chlorpyrifos and undergoes pH-dependent decomposition in water

(Drufovka et al. 2008, p. 295).

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Some species of zooplankton are affected by diazinon concentrations as low as 0.35 [micro]g/L (Amato et al, 1992, p. 214). From 1988 to 1990, the Central Valley Regional Water Quality Control Board conducted an aquatic toxicity survey in the San Joaquin Valley. Surface water samples collected from certain reaches of the San Joaquin River watershed during this survey were acutely toxic to the water flea,

Ceriodaphnia dubia (Foe and Connor 1991). The cause of toxicity was not determined but was attributed to pesticides in general. Further study was conducted in the Valley during the winter of 1991-92, and the resultant toxicity was attributed to the presence of chlorpyrifos and diazinon (Foe and Sheipline, 1993; Foe, 1995; Kuivila and Foe, 1995, p. 1149). Recognizing toxic concentrations of organophosphates can occur in tributaries to the San Joaquin and Sacramento River when agricultural areas contribute storm runoff, toxic concentrations rarely occur in the Sacramento River itself (MacCoy et. al 1995).

Although organophosphate pesticides commonly used in agricultural areas have been shown to be present in Delta waters and their tributaries at concentrations toxic to aquatic organisms (Werner et al. 2000, p. 226), little is known about the sensitivity of Sacramento splittail to these chemicals. Previous investigations of larval striped bass (Morone saxatilis) in the Delta indicated many larvae had been exposed to toxic compounds, potentially leading to slower growth and increased mortality rates (Bennett et al. 1995). It is possible that these contaminants also contribute to mortality and potentially affect juvenile splittail recruitment. Teh et al. (2005) conducted 96-hour acute toxicity tests on 7-day-old splittail larvae to determine the level of toxicity of orchard runoff water containing organophosphorus pesticides and observe potential biological effects. Spliital larvae were then transferred to clean water for three months to assess the survival, growth, histopathological abnormalities, and heat stress proteins. The results of although splittail larvae survived the 96 h exposure, Teh et al. (2005) observed exhibited reduced survival and growth and showed signs of cellular stress even after a three month recovery period.

Sublethal effects may play a more important role than acute mortality, but there is a lack of studies to identify and quantify sublethal responses to pesticides in splittail. In addition, although several studies have demonstrated the acute and chronic toxicity of two common dormant spray insecticides, diazinon and esfenvalerate, in other fish species (Barry et al. 1995, Goodman et al. 1979, Holdway et al. 1994, Scholz et al. 2000, Tanner and Knuth 1996), little work has been done integrating acute toxicity with biomarkers of exposure. Sublethal exposure to insecticides is expected to cause a wide range of responses

(biomarkers) in individuals ranging from genetic to reproductive anomalies. The addition of sublethal responses to routine acute toxicity testing may provide advanced warning of potentially significant environmental impacts and risks associated with organophosphate pesticides and prevent underestimation of effects on splittail populations. However, based upon the limited data available, we do not consider organophosphates to be a significant threat to the splittail population at this time. Although residual organophosphates will continue to be present in the ecosystem and site specific exposures will occur in localized areas that may affect individuals, the reduction of organophosphates discharged into the Delta due to EPA restrictions in recent years has greatly reduced the potential threat that organophosphates may have posed in the past (Luoma 2008, p. 64).

Pyrethroids

Pyrethroid use in the Central Valley has steadily increased since 1991 and reached an annual use of 80, 740 kilograms (kg) (178,000 pounds (lbs)) in 2003 (Oros and Werner 2005, p 11). Many farmers have switched from organophosphate-based insecticides to pyrethroid-based insecticides (which adhere to soil more strongly) due to a decision by the EPA to phase out organophosphates due to their toxicity to humans

(Luoma 2008, p. 64). Pyrethroids have a high absorption rate, andlow water solubility; they rapidly absorb to soil and organic matter

(Werner 2004, p. 2719). Although pyrethroids bioaccumulate, food web exposure is not considered a significant route of exposure to fish

(Hill 1985). The primary mode of transport for pyrethroids in aquatic systems is the adsorption of pyrethroids to surfaces of clay and soil particles that are suspended in the water column (Oros and Werner 2005, p 24). This combination of properties lends itself to accumulation of this substance in areas such as the Yolo Bypass.

All synthetic pyrethroids are potent neurotoxins that interfere with nerve cell function by interacting with voltage-dependent sodium channels as well as other ion channels, resulting in repetitive firing of neurons and eventually causing paralysis (Bradbury and Coats 1989, pp. 377-378; Shafer and Meyer, 2004). Pyrethroids are toxic to most aquatic invertebrates and fish, in many cases more toxic than the organophosphates they are replacing with LD50 values for aquatic organisms below 1 ppb (Smith and Stratton, 1986). The LD50 is the dose required to kill half the members of a tested population after a specified test duration. Aquatic insects are more sensitive to pyrethroids than fish, however, mollusks are relatively insensitive

(Clark et al., 1989). Acute effects of pyrethroids on aquatic insects could reduce available food resources for splittail. However, the magnitude of this potential effect is unknown and has not been studied.

Chronic exposures to pyrethroids can have significant impacts for immune function, reproductive success and survival for fish and their food organisms. Histopathological lesions in the liver were observed in splittail shortly (1 week) after 96-hour exposure to sublethal concentrations of organophosphate and pyrethroid insecticides. Fish recovered from these lesions, but showed high (delayed) mortality rates, grew slower and showed signs of cellular stress even after a 3 month recovery period (Teh et al. 2004b, p. 246).

Sub-lethal toxicity studies specific to splittail are limited but data exists for other fish species. One pyrethroid, esfenvalerate, exhibited both larval survival and immune effects in two fish species.

Delayed spawning and reduced larval survival of bluegill sunfish

(Lepomis macrochrius) were observed following two applications of 1 ppb of esfenvalerate (Tanner and Knuth 1996, pp. 246-250). Exposures of 0.08 ppb esfenvalerate dramatically increased the susceptibility of juvenile Chinook salmon (Oncorhynchus tshawytscha) to Infectious

Hematopoietic Virus (Clifford et al. 2005, pp. 1770-1771).

We conclude that although pyrethroids have been shown to have potential chronic to sub-lethal effects on individuals, there is no evidence to suggest that splittail exposures to pyrethroids in the

Estuary are having a significant effect at the population level.

Therefore we have determined that pyrethroids do not represent a substantial threat to splittail now or in the foreseeable future.

Ammonium

The effect of ammonia on aquatic organisms depends on its form.

Ammonia is un-ionized, and has the formula NH3. Ammonium is ionized, and has the formula NH4\+\. The major

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factors determining the proportion of ammonia or ammonium in water are water pH and temperature. This is important as the unionized NH3 is the form that can be toxic to aquatic organisms while NH4 is the form documented to interfere with uptake of nitrates (NO3) by phytoplankton

(Dugdale et al. 2007, Jassby 2008). The chemical equation that drives the relationship between ammonia and ammonium is:

NH3+ H2O [larr][rarr] NH4\+\ + OH-

When the pH is low, the reaction is driven to the right, and when the pH is high, the reaction is driven to the left. When temperature is high, the reaction is driven to the left and when temperature is low the reaction is driven to the right. Ammonia enters the Delta ecosystem through discharge from wastewater treatment plants, nitrogenous fertilizers, and atmospheric deposition. The largest source of ammonia entering the Delta ecosystem is the Sacramento Regional Wastewater

Treatment Plant (SRWTP), which accounts for 90 percent of the total ammonia load released into the Delta. Monthly loads of ammonium from the SRWTP released into the river have doubled from 1985 to 2005 resulting in 598 million liters (158 million gallons) per day discharged from the SRWTP during 2001-2005 (Jasby et al. 2008, p. 15).

Ammonia can be toxic to aquatic organisms and its acute and chronic effects are dependent on both pH and temperature. Ammonia is an oxygen demanding substance requiring oxygen for nitrification and could contribute to dissolved oxygen depletion in receiving waters. Effects of elevated ammonia levels on fish range from irritation of skin, gills, and eyes to reduced swimming ability and mortality (Wicks et al. 2002, p. 67). In addition to direct effects on fish, ammonia in the form of ammonium may alter the food web by adversely impacting phytoplankton and zooplankton dynamics in the Estuary ecosystem.

Ammonia can be toxic to several species of copepods important to larval and juvenile fishes; ammonium may impair primary productivity by reducing nitrate uptake in phytoplankton (Dugdale et al. 2007, pp. 27- 28).

A conceptual research framework has been prepared to improve understanding of the role of anthropogenic ammonia in the Bay-Delta ecosystem (Meyer et al. 2009, pp. 3-14). No studies to date address the effects of ammonia on splittail specifically. However, concerns related to synergistic effects from ammonia and other contaminants on splittail and other fish species in the Sacramento River have been raised. One study conducted at the University of California Davis Toxicology

Laboratory did not observe levels toxic to delta smelt, or two of its food organisms, in the Sacramento River downstream of SRWTP. However, treated effluent was found to be more chronically toxic than Sacramento

River water seeded with ammonium chloride to equal concentrations, suggesting that additional toxicants are present in SRWTP effluent

(Werner 2009, p. 21).

EPA is currently updating freshwater ammonia criteria that will include new discharge limits on ammonia (EPA 2009, pp. 1-46). There is no projected date for its adoption but a National Pollution Discharge

Elimination System (NPDES) permit for the SRWTP is being prepared by the California Central Valley Regional Water Quality Control Board for public notice in the fall of 2010. The NPDES permit is expected to include new ammonia limitations which will reduce loadings to the

Delta.

Although ammonia/ammonium is identified as a contaminant that is likely having a negative impact on the Estuary and may chronically or sub-lethally affect individual splittail within the population, there is no evidence that ammonia is having a population level effect on the species or will in the foreseeable future.

Summary of Contaminants

Most fish including splittail can be especially sensitive to adverse effects in their larval or juvenile stages when exposed to contaminants. Given splittail biology, adverse effects would be more likely to occur where sources of contaminants occur in close proximity to spawning and /or rearing habitats (i.e., floodplains, rivers and tributaries). Splittail are benthic feeders (feed on the bottom of water column) and are more susceptible than other fish to sediment contamination. They also face greater exposure to urban and agricultural runoff which tends to be concentrated in shoals where splittail reside (Moyle et al. 2004, p. 23).

Laboratory studies have shown certain contaminants to potentially have adverse effects on individual splittail. Field studies have shown that the contaminants of concern are elevated in the Delta and co-occur in areas important for splittail conservation. Although negative impacts to individual splittail from contaminants are suspected and have been shown on a limited basis, the overall extent of these impacts to the population remains largely unknown without further study and investigation. No information to date has conclusively shown that each of the contaminants identified above have a significant effect on splittail at the population level. In addition, several efforts are being undertaken to improve estuarine habitat and reduce the amount of contaminants discharged into the system. Therefore, we do not consider the contaminants of concern, as described above, to constitute an immediate threat to the species at this time or in the foreseeable future.

Climate Change

The Intergovernmental Panel on Climate Change (IPCC) has concluded that warming of the climate is unequivocal (2007, p. 5), and that temperature increase is widespread over the globe and is greater at northern latitudes (Soloman et al. 2007, p. 37). However, future changes in temperature and precipitation will vary regionally and locally, with some areas remaining unaffected or even decreasing in temperature.

Between 1995 and 2006, 11 of the 12 years have been the warmest on record (Soloman et al. 2007, p. 36). Over the next 20 years, climate models estimate that the Earth's average surface temperature will increase about 1.4 [deg]C (0.8 [deg]F). During the past decade, the average temperature in California, like that of much of the globe, was higher than observed during any comparable period of the past century

(Soloman et al. 2007, pp. 31-32). Nighttime air temperatures in

California have increased 0.18 [deg]C (0.33 [deg]F) per decade since 1920 while daytime temperatures have increased 0.05 [deg]C (0.1 [deg]F) per decade since 1920 (CEC 2009, p. 10).

By IPCC estimates for 2070-2099, California temperatures are expected to rise 1.6 to 2.7 [deg]C (3.0 to 5.5 [deg]F) under a low emissions scenario and 4.4 to 5.8 [deg]C (8.0 to 10.5[deg]F) under a high emissions scenario. However, recent studies have revealed that emissions are rising faster than even the most aggressive high emission scenarios used by IPCC in these calculations (CEC 2009 p. 41). Thus temperatures in the State are expected to rise faster than predicted unless global actions are taken to reduce emissions (CEC 2009 p. 41).

Similar to other California cyprinids, the splittail exhibits a high thermal tolerance. Acclimated fish can survive temperatures up to 33 [deg]C (91.4 [deg]F) for short periods of time (Young and Cech 1996, p. 670). Temperatures resulting from climate change in the next 50 years are not expected to stress splittail beyond their temperature range. Splittail have historically adapted to changes in the Delta system through

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migratory behavior and it is likely that they will continue to adapt and adjust their spawning and rearing grounds to areas with optimal temperature conditions (Moyle et al. 2004, p. 38).

Changes in precipitation are less certain than temperature; climate models project more frequent heavy precipitation events, separated by longer dry spells, especially in the western United States (IPCC 2007, p. 15). In California, snowfall in higher elevations has been increasing while snowfall in lower elevations has been decreasing

(CEC2009, p. 16). This has led to an overall decrease in run-off of 19 percent in the San Joaquin Basin and 23 percent in the Sacramento Basin between the months of April to July over the last 100 years, meaning more runoff is coming in earlier months (CEC 2009, p. 17). Overall,

California snowpack is predicted to decrease by 20 to 40 percent by the end of the century (CEC 2009, p. 44). However, due to the unpredictable nature of climate change, we are uncertain how the amount of run-off may vary over time and therefore we have no scientific evidence that potential drought conditions resulting from climate change pose a threat to the splittail.

Global sea level has risen at an average rate of 1.8mm (.07 inches) per year from 1961 to 2003, and an average rate of 3.1 mm (.12 in) year from 1993 to 2003 (IPCC 2007, p. 49). In California, sea level has risen about 18 cm (7 in) in the last century (CEC 2009, p. 24), which is similar to global sea level rise. The 2007 IPCC report modestly estimates that sea levels could rise by 0.18 to .58 m (0.6 to 1.9 feet) by 2100, but Rahmstorf (2007, p. 369) suggests that depending on the warming scenario employed, global sea level rise could increase by over 1.2 m (4 ft) in that time period (CEC 2009, p. 49). Even if emissions were halted today, oceans would continue to rise and expand for centuries because of their efficient heat storing abilities (CEC 2009, pp. 49-50). Current estimates put sea level rise at 20 to 50 cm (8 to 19 in) by 2050, which is likely to contribute to the flooding of at least some Delta islands (Knowles 2010, pers. comm.).

The San Francisco estuary will be more susceptible to sea-level rise due to its narrow bays and channels and because it already lies below or at sea level (Moyle et al. 2004, p. 38). Many of the Delta islands used for agriculture have been drained and armored with levees for flood protection and groundwater level maintenance. These reclamation and agricultural activities have caused island surface levels to subside due to rapid decomposition of their water logged peat soils. Many of the central and western Delta islands have experienced the most subsidence, now lying at 3 to 7.6 m (10 to 25 ft) below sea level (Ingebritsen et al. 2000, p. 2). These islands are at a high level risk from sea level rise because, as islands subside and water levels rise, levee banks are experiencing greater hydrostatic force, thereby increasing the risk of their failure.

Earthquake fault models also show a high degree of risk of a significant seismic event that could affect the islands in the central and western Delta (Mount et al. 2005, p. 13). Failure of the levees on some or all of these islands, as a result of liquefaction of the unstable soils that make up the levees' foundations during an earthquake, could turn part or the entire Delta into a brackish bay in the future. The encroaching ocean would increase salinity levels in the central and western Delta, with the result that the range of splittail would likely be curtailed to some location upstream of the confluence of the Sacramento and San Joaquin rivers.

Due to the divergence of two splittail population segments, one population is exposed to higher salinities in the Napa and Petaluma river systems for at least part of its life cycle (Feyrer et al. 2010, p. 12). This population may be better able to adapt to increased salinity levels that sea level rise may bring. Splittail have an unusually high salinity tolerance and populations have shown great resilience in waters with variable salinities (Moyle et al. 2004, p. 38; Young and Chech 1996, p. 673). Abundance indices soared in 1995 and 1998, in response to wet hydrological years following a decade of predominantly dry conditions, showing the resilience of this species.

One problem climate change may pose to splittail is the reduced spawning habitat due to deeper water (Moyle et al. 2007, p. 38).

However, new spawning habitat that may be created as a result of flooding will help to accommodate splittail spawning in the event of rising ocean levels. Liberty Island (discussed under Factor A) is one example of the benefits that island flooding could have on splittail if correctly managed. Under predicted future flooding conditions, splittail could spawn in the Sutter Bypass and rear in the Delta.

Splittail have adapted to changes in the ecosystem through their migratory behavior (Moyle 2004, p. 38) and may continue to do so in the future.

Introduced Species

Copepods (E. affinis, Pseudodiaptomus forbesi), a major prey item for splittail, have declined in abundance in the Delta since the 1970s

(Kimmerer and Orsi 1996, p. 409). Starting in about 1987, declines were observed in the abundance of phytoplankton (Alpine and Cloern 1992, p. 951). These declines have been partially attributed to grazing by the overbite clam (Corbula amurensis) (Kimmerer et al. 1994, p. 86) which became abundant in the Delta in the late 1980s. Asiatic clams

(Corbicula fluminea) can exceed 200,000 per square meter (m2) and overbite clam abundance can exceed 10,000 per m2 (Kimmerer et al. 2008, p. 82). Because the overbite clam consumes copepod larvae as it feeds, it not only reduces phytoplankton biomass but also competes directly with splittail for food (Kimmerer et al. 1994, p. 87). It is believed that these changes in the estuarine food web negatively influence pelagic fish abundance, including splittail abundance. In the Delta, phytoplankton production has declined 43 percent between 1975 and 1995

(Jasby et al. 2002, p. 703). The correlation of phytoplankton decline with the appearance of the overbite clam leads us to believe that the overbite clam is overgrazing the system.

Three non-native species of copepods (Sinocalanus doerrii,

Pseudodiaptomus forbesi, and Pseudodiaptomus marinus) became established in the Delta between 1978 and 1987 (Carlton et al. 1990, pp. 81-94), while native Eurytemora affinis populations have declined since 1980. It is not known whether these non-native species have displaced E. affinis or whether changes in the estuarine ecosystem now favor S. doerrii and the two Pseudodiaptomus species. Meng and Orsi

(1991) reported that S. doerrii is more difficult for larval striped bass to catch than native copepods because S. doerrii is fast swimming and has an effective escape response. It is not known whether this difference in copepod swimming and escape behavior has affected the feeding success of young splittail.

Limnoithona tetraspina (no common name) is a nonnative copepod that began increasing in numbers in the delta in the mid 1990s, about the same time that P. forbesi began declining (Bennett et al. 2005, p. 18).

L. tetraspina is now the most abundant copepod species in the low salinity zone (Bouley and Kimmerer 2006, p. 219), and is likely an inferior prey species for splittail because of its smaller size and superior predator avoidance abilities when compared to P. forbesi

(Bennett et al. 2005, p. 18; Baxter et al. 2008, p. 22).

Splittail have shifted their diet to utilize non-native species.

Although the

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non-native copepods and bivalves discussed above have altered the food web in the Delta ecosystem, we have no compelling evidence to suggest that this has led to a decline in the splittail population. Please refer to the bioaccumulation section for a full analysis of the effects on splittail due to a shift in prey base from native species to the overbite clam.

Chinese mitten crabs (Eriocheir sinensis) could reach concentrations sufficient to intermittently impede the operation of fish screens and salvage facilities, thus reducing the effectiveness of splittail salvage and repatriation efforts. The US Bureau of

Reclamation has installed a device, known as ``Crabzilla'' to remove

Chinese mitten crab from their CVP fish salvage facility. However,

Chinese mitten crabs have not appeared in large numbers at either of the fish salvage facilities in recent years. As a result of the apparent decline of this nonnative species subsequent to their initial appearance in the Delta, along with the measures taken at the CVP fish salvage facility, the existence of the Chinese mitten crab in the Delta is not a current threat to splittail.

Of some concern is the presence of Brazilian pondweed (Egeria densa) and water hyacinth (Eichhornia crassipes), both of which tend to form dense near-shore and slough-wide mats of vegetation that serve as retreat, foraging, and ambush sites for splittail predators. These vegetation mats also may divert upstream- and downstream-migrating splittail into channels rather than the more-productive bankside habitat by creating an obstacle (Moyle et al. 2004, p. 29).

Summary of Factor E

In summary, splittail are not significantly threatened by water export facilities, agricultural and power plant diversions, poor water quality, environmental contaminants, climate change, or introduced species.

Operation of the CVP and SWP water export facilities directly affects fish by entrainment into their diversion facilities. CVP and

SWP dams and diversions changed the historical hydrological features of the watershed systems, have altered and eliminated habitat for splittail, and may have reduced the distribution of the splittail by restricting movement to potential spawning grounds and creating migration obstacles. Entrainment at SWP and CVP pumps has not been demonstrated to affect splittail at the population level because loss of substantial numbers of fish tends to occur during wet years in which the species is experiencing a high reproductive output. CALFED's

Ecosystem Restoration Program (discussed under Factors A and E, above) has been successful in restoring habitat for the splittail and reducing threats from entrainment at water diversion sites.

Splittail can become entrained in agricultural water diversions resulting in injury or mortality. Under both the CALFED Bay-Delta

Program and the Central Valley Project Improvement Act, there have been significant efforts to screen agricultural diversions in the Central

Valley and the Sacramento-San Joaquin Delta, and studies have found splittail entrainment to be exceptionally low. We do not consider entrainment by agricultural diversions to be a significant threat to splittail.

Two power plants located near the confluence of the Sacramento and

San Joaquin rivers pose an entrainment risk to splittail. The intakes for the cooling water pumps of these power plants are located in close proximity to splittail rearing habitat (Moyle et al. 2004, p. 20).

Thermal and chemical pollution may also have a detrimental effect on splittail (USFWS 2008, pp. 173-174). However, due largely to the reduction in the operation of the power plants and their associated pumping for cool water, we do not consider the operation of these power plants to constitute a significant threat to the splittail population.

We have no indications of future plans to use these pumps more frequently and therefore do not consider these operations to be a threat in the future.

Laboratory studies have shown certain contaminants to be detrimental to individual splittail and the co-occurrence of splittail with contaminants has been documented. Although negative impacts to individual splittail from contaminants have been shown, the overall extent of such cases, and impacts to the population as a whole, remain largely undocumented. No studies to date have shown contaminants to have a significant effect on splittail at the population level.

Bioaccumulation of selenium and mercury in the overbite clam is occurring and the overbite clam is a substantial prey item for splittail. However, we have no evidence that the bioaccumulation of selenium or mercury is having a detrimental effect on splittail at the population level or will in the foreseeable future.

Climate change in California is expected to bring increased temperatures, changes in precipitation and run-off, and increased salinity levels associated with sea level rise. These changes may restrict splittail range or reduce spawning habitat. However, splittail exhibit high thermal salinity tolerances and are known to adapt to changes in the Delta through migratory behavior. In addition, new spawning habitat may be created as a result of flooding. We have no scientific evidence that potential drought conditions resulting from climate change pose a threat to the splittail.

Introduced species are having an effect on the food web and ecology of the Estuary. Bivalves such as the overbite clam have displaced native food sources of the splittail. However, splittail have shifted their diets to utilize non-native food sources. Although the non-native copepods and bivalves discussed above have altered the food web in the

Delta ecosystem, we have no compelling evidence to suggest that this has led to a decline in the splittail population.

We conclude that the best scientific and commercial information available indicates that the Sacramento splittail is not now, or in the foreseeable future, threatened by other natural or manmade factors affecting its continued existence.

Finding

As required by the Act, we considered the five factors in assessing whether the Sacramento splittail is endangered or threatened throughout all or a significant portion of its range. We have carefully examined the best scientific and commercial information available regarding the past, present, and future threats faced by the Sacramento splittail. We reviewed the petition information available in our files, reviewed other available published and unpublished information, and consulted with recognized Sacramento splittail experts and other Federal, State, and tribal agencies, including the California Department of Fish and

Game and the U.S. Bureau of Reclamation.

We identified and evaluated the risks of the present or threatened destruction, modification, or curtailment of the habitat or range of the Sacramento splittail. The rate of habitat loss in the Estuary that occurred the 1900's is no longer occurring today and efforts undertaken in the past decade have benefited the species by restoring its habitat.

There is presently sufficient habitat to maintain the species; inundation frequency and duration in key areas is sufficient to provide spawning to maintain the species. The implementation and magnitude of the CALFED, CVPIA (discussed under Factor D) and other habitat restoration activities, which focus on the restoration of habitats that directly and

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indirectly benefit splittail are greater than any foreseeable future habitat losses. The overall effect of habitat restoration activities is also expected to continue to be beneficial for splittail into the foreseeable future. Based on a review of the best scientific information available, we find that the present or threatened destruction, modification, or curtailment of Sacramento splittail habitat or range (Factor A) is not a significant threat to the splittail now or in the foreseeable future.

The new CDFG regulation enacted in March 2010 limiting take of splittail to two individuals per day has eliminated any potential threat that fisheries may have posed. There is no indication that the current level of scientific take adversely affects the splittail population, and there is no indication that the level of mortality will increase in the future. Based on a review of the best scientific information available, we find that overutilization for commercial, recreational, scientific, or educational purposes (Factor B) is not a significant threat to the Sacramento splittail. We found disease occurs at low levels in the population, but does not constitute a significant threat to the species (Factor C). Predation by striped bass appears to be unchanged from past levels, is currently not a significant threat to splittail populations, and is not expected to increase in the future.

Largemouth bass populations have increased in the Estuary in the past three decades, but populations of largemouth bass in critical rearing areas are low, therefore predation levels appear to be minor. Based on a review of the best scientific information available, we find that disease and predation (Factor C) are not significant threats to the

Sacramento splittail, now or in the foreseeable future.

Federal and State regulations provide protection for the splittail and its habitat by limiting adverse effects from new projects, restoring habitat and limiting contaminants discharged into the

Estuary. Based on a review of the best scientific information, we find that a lack of regulatory mechanisms (Factor D) does not constitute a significant threat to the Sacramento splittail population now or in the foreseeable future.

Based on the best available science, we find that other natural or manmade factors affecting the continued existence of the splittail (as described under Factor E) have not been shown to be significant threats to the splittail at this time. Furthermore, there is no evidence to suggest that these factors will increase and become threats to the splittail in the foreseeable future. Splittail are not threatened by water export facilities, agricultural and power plant diversions, poor water quality, environmental contaminants, climate change, or introduced species (Factor E). Entrainment at SWP and CVP pumps has not been demonstrated to affect splittail at the population level. CALFED's

Ecosystem Restoration Program (discussed under Factors A and E above), the CVPIA, and the provisions of the OCAP BOs, have been successful in reducing threats from entrainment at water diversion sites. Under both the CALFED Bay-Delta Program and the Central Valley Project Improvement

Act, there have been significant efforts to screen agricultural diversions in the Central Valley and the Sacramento-San Joaquin Delta, and studies have found splittail entrainment to be exceptionally low.

Therefore, we do not consider entrainment by agricultural diversions to be a significant threat to splittail. Due to reduction in the operation of two power plants and their associated pumping for cool water, we do not consider the operation of these power plants to constitute a significant threat to the splittail population. We have no indications of future plans to use these pumps more frequently and therefore do not consider these operations to be a threat in the future.

Laboratory studies have shown certain contaminants to be detrimental to individual splittail and the co-occurrence of splittail with contaminants has been documented. Although negative impacts to individual splittail from contaminants have been shown, the overall extent of such cases, and impacts to the population as a whole, remain largely undocumented. No studies to date have shown contaminants to have a significant effect on splittail at the population level.

Bioaccumulation of selenium and mercury in the overbite clam is occurring and the overbite clam is a substantial prey item for splittail. However, we have no evidence that the bioaccumulation of selenium or mercury is having a detrimental effect on splittail at the population level or will in the foreseeable future.

The existing data fails to show a significant long term decline of the species. Natural fluctuations of population levels do not constitute an overall decline in the species, but rather show a pattern of successful spawning during wet years followed by reduced spawning during dry years. The model deployed in this finding simulates the species fluctuations and is compatible with known life history traits of the species. Population levels are directly correlated with inundation of floodplains and simulation models predict that these habitats must flood at a minimum of every 7 years for the species to persist in sufficient numbers to maintain a robust population level

(Moyle et al. 2004, p. 38). We have no evidence to show that the frequency of inundation events on floodplains will decrease to the point that these events will not be sufficient to maintain robust population levels. Therefore, based on the best available data, we do not find an overall declining trend in the species' population.

Although global warming will change hydrography in the Delta, predictions do not foresee an imminent reduction in flooding of the

Yolo Bypass. Splittail have continually adapted to changes in the ecosystem including salinity variation and we have no evidence to show that this will not continue to be the case. The Yolo and Sutter

Bypasses and the Cosumnes River floodplain are serving as refuge for the species and there is no evidence that these areas will not continue to do so in the future. These floodplains are currently being expanded through public and private partnerships including CALFED ERP, CVPIA,

Cosumnes River Preserve restoration efforts, and the acquisition and restoration of Liberty Island.

Our review of the best available scientific and commercial information pertaining to the five threat factors, does not support a conclusion that there are independent or cumulative threats of sufficient imminence, intensity, or magnitude to indicate that the

Sacramento splittail is in danger of extinction (endangered), or likely to become endangered within the foreseeable future (threatened), throughout its range. Therefore, listing the Sacramento splittail as endangered or threatened is not warranted at this time.

Distinct Vertebrate Population Segments

After assessing whether the species is endangered or threatened throughout its range, we next consider whether a distinct vertebrate population segment (DPS) exists and meets the definition of endangered or is likely to become endangered in the foreseeable future

(threatened).

Under the Service's DPS Policy Regarding the Recognition of

Distinct Vertebrate Population Segments Under the Endangered Species

Act (61 FR 4722; February 7, 1996), three elements are considered in the decision concerning the establishment and classification of a possible DPS. These are applied similarly for additions to or removal from the Federal List of

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Endangered and Threatened Wildlife. These elements include:

(1) The discreteness of a population in relation to the remainder of the taxon to which it belongs;

(2) The significance of the population segment to the taxon to which it belongs; and

(3) The population segment's conservation status in relation to the

Act's standards for listing, delisting, or reclassification (i.e., is the population segment endangered or threatened).

In this analysis, we will evaluate whether the San Pablo population of splittail is a DPS. This analysis is being conducted because recent studies by Baerwald et al. (2007) have revealed genetic variation between the San Pablo and Delta populations of splittail. The San Pablo population of splittail represents a fraction of the overall splittail population. For the purposes of this analysis, splittail individuals that spawn in the Napa and Petaluma rivers will be referred to as the

San Pablo population and individuals that spawn in other rivers including the Sacramento, San Joaquin and Cosumnes rivers will be referred to as the Delta population.

Discreteness

Under the DPS policy, a population segment of a vertebrate taxon may be considered discrete if it satisfies either one of the following conditions:

(1) It is markedly separated from other populations of the same taxon as a consequence of physical, physiological, ecological, or behavioral factors. Quantitative measures of genetic or morphological discontinuity may provide evidence of this separation.

(2) It is delimited by international governmental boundaries within which differences in control of exploitation, management of habitat, conservation status, or regulatory mechanisms exist that are significant in light of section 4(a)(1)(D) of the Act.

The data used to determine genetic differences between two splittail populations were collected in 2002 and 2003 and first published in (Feyrer et al. 2005, pp. 164-167) to show upstream distribution limits of splittail. Young of the year splittail individuals were collected from the Napa, Petaluma, Cosumnes,

Sacramento and San Joaquin rivers and salinities were recorded at these sites. Individuals collected from the farthest upstream locations on the rivers were chosen for genetic analysis in an attempt to ensure that they were collected in the natal rivers in which they were spawned

(Baerwald et al. 2007, p. 160).

Baerwald et al. (2007) used 13 microsatellite markers to genetically distinguish 489 young-of-the-year splittail collected from these five drainage areas (2007, pp. 160-161). Two genetically distinct populations were found, one in the Napa/Petaluma (San Pablo population) drainages and one in the greater Central Valley drainages (Delta population) (Baerwald et al. 2007, p 162). Microsatellite markers are neutrally inherited. Neutrally inherited genes come from the mother and are always passed on to the next mother, where as the fathers genes may or may not be passed on. The most likely reason for finding a statistical difference in gene frequencies is isolation of spawning populations (Israel and Baerwarld et al., 2010, pers. comm.). Both splittail populations use Suisun Bay as rearing habitat in the nonspawning season; however Suisun Marsh was used as foraging ground almost exclusively by the Delta population (Baerwald et al. 2008, p. 1341). The majority (88 percent) of individuals collected foraging in

Suisun Marsh assigned to the Delta population; however, less association was seen in individuals in the Ryer and Chipps Islands with 54 to 74 percent assigning to the Delta population (Baerwald et al. 2008, p. 1341). Although some overlap in foraging grounds was observed, these populations largely maintain themselves in different habitats and possess different genetic make-ups.

Thus, these studies demonstrate that the San Pablo population segment, composed of individuals from the Napa and Petaluma rivers, is markedly separate from the Delta population segment composed of individuals from the Sutter Bypass and Sacramento, Cosumnes and San

Joaquin rivers as a consequence of genetic variation (Baerwald et al. 2007, pp. 164-165). Baerwald et al. noted that their results appear to be correlated with differences in salinities between spawning grounds and migration routes. Our analysis of the peer reviewed work done by

Baerwald et al. (2007 and 2008) leads us to conclude that the San Pablo population is discrete under the Service's DPS policy.

Significance

If a population segment is considered discrete under one or more of the conditions described in the Service's DPS policy, its biological and ecological significance will be considered in light of

Congressional guidance that the authority to list DPSes be used

``sparingly'' while encouraging the conservation of genetic diversity.

In making this determination, we consider available scientific evidence of the discrete population segment's importance to the taxon to which it belongs. Since precise circumstances are likely to vary considerably from case to case, the DPS policy does not describe all the classes of information that might be used in determining the biological and ecological importance of a discrete population. However, the DPS policy describes four possible classes of information that provide evidence of a population segment's biological and ecological importance to the taxon to which it belongs. As specified in the DPS policy (61 FR 4722), this consideration of the population segment's significance may include, but is not limited to, the following:

(1) Persistence of the discrete population segment in an ecological setting unusual or unique to the taxon;

(2) Evidence that loss of the discrete population segment would result in a significant gap in the range of a taxon;

(3) Evidence that the discrete population segment represents the only surviving natural occurrence of a taxon that may be more abundant elsewhere as an introduced population outside its historic range; or

(4) Evidence that the discrete population segment differs markedly from other populations of the species in its genetic characteristics.

A population segment needs to satisfy only one of these conditions to be considered significant. Furthermore, other information may be used as appropriate to provide evidence for significance.

(1) Persistence of the discrete population segment in an ecological setting unusual or unique to the taxon.

Salinity concentrations were recorded between April and July in 2002 and 2003 on the Sacramento, San Joaquin, Napa, and Petaluma rivers at various locations where splittail were collected. Salinity concentrations on the Petaluma River averaged 13.0 ppt in 2002 and 6.0 ppt in 2003. Napa River salinity concentrations averaged 5.0 ppt in 2002 and 0.0 ppt in 2003. The San Joaquin and Sacramento rivers averaged 0.0 ppt for both years (Baerwald et al. 2008, p. 165).

Sacramento and San Joaquin rivers never contained salinity concentrations higher than 1.0 ppt. Salinity concentrations on the Napa

River ranged between 0.0-8.5 ppt while Petaluma River salinity concentrations ranged between 5.5-14.1 ppt (Feyrer et al. 2010, p. 8).

It is speculated that high salinities are creating a barrier between these populations that is only broken during high outflow years (Feyrer et al. 2010, p. 11). This barrier likely occurs

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in the area of Carquinez Straight between Suisun Bay and San Pablo Bay.

Napa River populations mostly associate with the San Pablo population although a small number of individuals caught in 2003 when the salinity was 0.0 ppt on the Napa River associated with the Delta population. The presence of the Delta population in the Napa River in 2003, when the salinity was 0.0 ppt and absence in 2002 when salinities were higher may reflect the Delta population's limited ability to tolerate high salinities for spawning.

The data we have clearly shows that the Napa and Petaluma rivers had higher salinities than other areas of the Delta where the splittail persists for the 2 years that surveys were conducted. However, we feel that 2 years of data are not sufficient to conclude that this constitutes a unique ecological setting that is persistent over time. A larger data set covering more years is needed to assess the salinities of these rivers particularly at splittail spawning grounds before we can conclude the range of the San Pablo population constitutes a unique ecological environment. Therefore, we are lacking convincing evidence that shows the San Pablo population persists in an unusual or unique ecological setting that contributes significantly to the taxon at this time.

(2) Evidence that loss of the discrete population segment would result in a significant gap in the range of a taxon;

The San Pablo population segment is on the western edge of the species range and only constitutes a small portion of the species range. Loss of this population would not create a gap in the remainder of the species range because the San Pablo population does not provide for connectivity with other portions of the range. Therefore, we conclude that loss of this population would not represent a significant gap in the range of the species.

(3) Evidence that the discrete population segment represents the only surviving natural occurrence of a taxon that may be more abundant elsewhere as an introduced population outside its historic range.

This criterion does not apply to the San Pablo splittail population because it is not a population segment representing the only surviving natural occurrence of the taxon that may be more abundant elsewhere as an introduced population outside its historical range.

(4) Evidence that the discrete population segment differs markedly from other populations of the species in its genetic characteristics.

Under the DPS policy we measure the evidence for potential biological and ecological significance to the species as a whole, as reflected by marked differences in its genetic characteristics.

Evidence that the discrete population segment differs markedly from other populations of the species in its genetic characteristics is provided in the Baerwald et al study. (2007, p. 166). These genetically distinct populations may be driven by the strong selective pressure separating out species that are salinity tolerant from those that are susceptible to salinity effects (Baerwald et al. 2007, p. 165). We conclude that the San Pablo population of splittail meets this criterion of the DPS policy because it differs markedly from other populations in its genetic characteristics.

Determination of Distinct Population Segment

Based on the best scientific and commercial information available, as described above, we find that under the Service's DPS policy, the

San Pablo population segment is discrete and is significant to the taxon to which it belongs. Evidence that the San Pablo splittail is biologically and ecologically significant from other populations of splittail is based on the evidence that the discrete population segment differs markedly from other populations of the species in its genetic characteristics. Because the San Pablo population segment is both discrete and significant, it qualifies as a DPS under the Act.

Distinct Population Segment Five-Factor Analysis

Since the San Pablo population segment qualifies as a DPS, we will now evaluate its status with regard to its potential for listing as endangered or threatened under the five factors listed in section 4(a) of the Act. The majority of the factors affecting the species throughout its range also affect the San Pablo DPS of splittail. These factors can be found in the five factor analysis conducted for the entire range of the splittail found above. Our evaluation of the San

Pablo DPS follows.

Factor A. The present or threatened destruction, modification, or curtailment of its habitat or range

Habitat Loss

Rapid development within the San Pablo DPS' range began with the discovery of gold in the Sierra Nevada foothills in the 1850s.

Hydraulic mining operations contributed huge amounts of sediment to San

Pablo Bay. For the next hundred years, the marshes were filled, diked, or drained to support the bay's development as a major center of commerce. About 85 percent of the historic tidal marshes of San Pablo

Bay have been altered, negatively affecting the ability of the remaining tidal marshes to accept winter rainfall and purify water in the bay.

Beneficial Actions Offsetting Adverse Effects

Since the 1960s, State and government agencies, non-profit organizations, and local grassroots organizations have made efforts to protect and restore San Pablo Bay. The San Pablo Bay National Wildlife

Refuge was established in 1974 and currently protects over 13, 000 acres of wildlife habitat. Largely comprised of thousands of acres of tidelands leased from the California State Lands Commission, the refuge's ultimate plans include protection and conservation of more than 8,094 ha (20,000 ac) of critical wildlife in northern San Pablo

Bay (FWS Brochure 2001, pp. 1-6). Additional efforts are underway to protect and restore the bay. The San Pablo Bay Preservation Society is currently working to acquire land on San Pablo point (http:// www.pointsanpablo.org/) and the friends of San Pablo Bay NWR have helped to establish a nursery that is being used to re-vegetate tidal wetlands.

Although the historic loss of floodplains has detrimentally affected the species in the past, current laws and protections including the creation of the San Pablo Bay National Wildlife Refuge have largely eliminated future losses of floodplain to the splittail.

Many of the natural floodplains in the Napa and Petaluma rivers are still intact and provide optimal spawning grounds to splittail. The San

Pablo DPS is much closer to the ocean than the Delta DPS and is largely influenced by a tidal system. Fresh water input into the system is essential to provide proper salinity levels. Over the past 100 years, fresh water input has been reduced by diversions and water barriers.

Although, this reduction in fresh water flow has changed salinity concentrations in the Napa and Petaluma rivers, we have no evidence to suggest that it has had a significant effect on the population level of the species.

Recent Abundance Data Trends

On June 1, 2010, splittail individuals encompassing both young-of- the-year (less than 1 year in age) and age one

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were captured in the Petaluma River (Sommer et al. unpublished, pp. 1- 3). The presence of splittail from two different age classes makes it likely that splittail successfully spawned in the Petaluma River in 2010 (a relatively wet year) and 2009 (a critically dry year). This shows that splittail are persisting in the Petaluma River. In addition, all 10 of the fish captured in the survey belonged to the San Pablo population of splittail. During this survey, fish were collected at two out of three survey sites. During previous surveys in the Petaluma

River, splittail were captured at one out of three sites (Feyrer et al. 2005, p. 162).

We have no evidence at this time to suggest that the San Pablo population of splittail is in decline. The accepted range of the species in the Napa and Petaluma rivers has increased as new surveys have found presence of splittail in areas where they were previously not believed to be in the mid-1990's (Sommer et al. 2007, p. 28).

Summary of Factor A

Although there has been substantial loss of habitat historically, present and future loss of habitat is expected to be minimal due to current land protections including the San Pablo Bay National Wildlife

Refuge. Efforts undertaken in the past decade have benefited the species by restoring its habitat. There is presently sufficient habitat to maintain the species, inundation frequency and duration in key areas is sufficient to provide spawning to maintain the species. We conclude that the best scientific and commercial information available indicates that the San Pablo DPS of Sacramento splittail is not now, or in the foreseeable future, threatened by the present or threatened destruction, modification, or curtailment of its habitat or range.

Factor B. Overutilization for commercial, recreational, scientific, or educational purposes

Recreational Fishing

Take of splittail due to fisheries is a potential threat rangewide to the species and this threat is not expected to be any different for the San Pablo DPS. Please refer to Factor B in the rangewide analysis for a full discussion of take due to recreational fishing. Take due to recreational fishing is not considered to be a substantial threat to the San Pablo DPS of splittail at this time.

Scientific Collection

Take and fatalities attributed to scientific sampling in areas occupied by the San Pablo population of splittail are far less than the rangewide take of the species. There have only been 10 known surveys of the San Pablo DPS splittail in the last 10 years. These include five

U.S. Army Corp of Engineers' surveys (2001 and 2002), three surveys conducted by Feyrer et al.(2002, 2003 and 2010) and one study by the

Napa Creek Floodplain Project (2007). There were a total of 4 splittail captured in 2001 (USACE 2002), 79 captured in 2002 (USACE 2002), 48 captured in 2003 (USACE 2004), 326 captured in 2004 (USACE 2004), and 305 captured in 2005 (USACE 2006) by the Army Core of Engineers. None of the fish captured by the Corps were kept. The amounts of Yyung-of- the-year captured in the Feyrer et al. studies were: 112 in the Napa

River and 45 in the Petaluma River in 2002, and 62 in the Napa River and 171 in the Petaluma River in 2003 (Feyrer 2010, pers. comm.).

During a short gill net study in 2003, Feyrer et. al. collected 108 adult splittail (Feyrer 2010, pers. comm.). A total of 13 splittail were captured in 2010. All of the splittail taken in the Feyrer et al. studies were preserved for genetic analyisis. There were seven splittail caught in the Napa Creek Floodplain Project study in June of 2007 (Turner 2007). Female splittail can lay up to 100, 000 eggs in a single spawning event and the take of several hundred individuals is not expected to effect the population at the species level. Therefore, scientific take is not considered to be a significant threat to splittail at this time, however, scientific studies regarding the San

Pablo population of splittail have been kept to a minimum to be sure not to threaten the limited number of individuals present in this population (Feyrer et al. 2010, pers. comm.)

Summary of Factor B

The new CDFG regulation enacted in March 2010 limiting take of splittail to two individuals per day has eliminated any potential threat that fisheries may have posed. There is no indication that the current level of scientific take adversely affects the splittail population, and there is no indication that the level of mortality will increase in the future. We conclude that the best scientific and commercial information available indicates that the San Pablo DPS of the Sacramento splittail is not now, or in the foreseeable future, threatened by overutilization for commercial, recreational, scientific or educational purposes.

Factor C. Disease or predation

Disease

Disease is a potential threat to splittail rangewide including in the San Pablo Bay and the potential threat of disease is expected to be the same in scope and intensity as it is in the overall range of the population. Please refer to Factor C in the range wide analysis for a full discussion of the effects of disease on splittail. Based on a review of the best scientific information available, we find that disease is not a significant threat to the San Pablo Bay population of splittail now or in the foreseeable future.

Predation

The salinity level in San Pablo Bay and the Napa and Petaluma rivers serves as a barrier to potential predators of the San Pablo DPS of splittail. Predators such as largemouth bass and catfish are not able to tolerate the high salinity environment present in the area of the San Pablo Bay population. The only substantial predator of splittail that is able to reside in this environment is the striped bass (Nobriga 2010, pers. comm.).

Based on a review of the best scientific information available, we find that predation is not a significant threat to the San Pablo Bay population of splittail now or in the foreseeable future.

Summary of Factor C

We found disease occurs at low levels in the population, but does not constitute a significant threat to the species. Because the potential threat of predation on the San Pablo DPS of splittail is expected to be less than the potential threat on the overall population due to a salinity barrier, we conclude that predation is not a significant threat to the San Pablo population now or in the foreseeable future. We conclude that the best scientific and commercial information available indicates that the San Pablo Bay DPS of the

Sacramento splittail is not now, or in the foreseeable future, threatened by disease or predation.

Factor D. The inadequacy of existing regulatory mechanisms

State Laws

State laws acting as existing regulatory mechanisms are expected to provide the same protections to the San Pablo Bay DPS of splittail as they do to the entire range of the species because the laws are uniform throughout the State of California. Please refer to Factor D in the rangewide analysis for a full discussion of the State laws acting as

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existing regulatory mechanisms to provide protections to the splittail.

Federal Laws

Federal laws acting as existing regulatory mechanisms are expected to provide the same protections to the San Pablo Bay DPS of splittail as they do to the entire range of the species because the laws are uniform throughout the United States. Please refer to Factor D in the rangewide analysis for a full discussion of the Federal laws acting as existing regulatory mechanisms to provide protections to the splittail.

Summary of Factor D

Federal and State regulations described in the analysis of the entire species range provide protection for the splittail and its habitat by limiting adverse affects from new projects, restoring habitat and limiting contaminants discharged into the Estuary. Although the Act does not directly regulate actions in splittail habitat, the provisions in the Act that apply to other listed species benefit the splittail. We conclude that the best scientific and commercial information available indicates that the San Pablo DPS of the

Sacramento splittail is not now, nor in the foreseeable future, threatened by inadequate regulatory mechanisms.

Factor E. Other natural or manmade factors affecting its continued existence

We have identified the risk of water export facilities, agricultural and power plant diversions, poor water quality, environmental contaminants, climate change, or introduced species as potential threats to the San Pablo DPS of splittail.

Water export facilities

Water export facilities (CVP and SWP pumps) and power plant diversions which were analyzed in the range wide splittail finding are not located within the range of the San Pablo DPS and therefore do not represent potential threats to the San Pablo DPS. Water export facilities do not exist in the area of the San Pablo DPs and therefore are not considered to be a substantial threat to splittail now or in the foreseeable future.

Agricultural Diversions for Irrigation

Agricultural diversions are a potential threat range wide to splittail including in the area occupied by the San Pablo DPS. The majority of agricultural diversions in the Napa River are utilized by wineries for the production of grapes. Wine production in the Napa

Valley is a multimillion dollar industry. There are a total of 1200 agricultural diversions in Napa County. Of these, there are 99 active diversions in the Napa River itself and they are primarily attributed to wine production (California integrated water quality systems 2010, p. 1). Splittail populations are persisting in the Napa and Petaluma

Rivers and we have no data to show that agricultural diversions are a significant threat to the continued existence of the species at the population level now or in the foreseeable future.

Power Plant Diversions

There are no power plant diversions within the range of the San

Pablo DPS of splittail. The Contra Costa Power Plant and the Pittsburg

Power Plant (discussed in the rangewide analysis) are not a factor because they are located outside of the range of the San Pablo DPS of splittail. Power plant diversions are not expected to be a threat to the San Pablo population of splittail now or in the foreseeable future.

Water Quality and Environmental Contaminants

The Napa River exhibits a high eutrophication rate and has been placed on California List of Impaired Water Bodies (303(d) list) because nutrients, pathogens and sedimentation. The Petaluma River is on the California List of Impaired Water Bodies (303(d) list) for possessing high elevations of diazinon, nutrients, and sedimentation.

The primary symptom of excessive nutrient loading in this watershed is dense algae growth. Eutrophication occurs when high nutrient levels increase growth of plant and algal matter resulting in dissolved oxygen removal from the system when the plants die and begin to decompose

(Wang et al. 2004, p. 10).

Efforts are underway by State water resource staff to address many nutrient sources including faulty septic systems, agricultural and urban runoff, and livestock through regulatory programs. These programs will address multiple pollutants, including pathogens, nutrients, and sediment. The Napa County resource conservation district has ongoing restoration efforts including native plant re-vegetation, road improvements, fish barrier removal, upland habitat improvements, and stream and wetland restoration. A Napa sustainable winegrowing group is active in educating wine growers on the benefits of reducing pesticide use and promoting soil health through erosion control.

Although the Napa and Petaluma rivers do exhibit a high amount of nutrients, we have no evidence at this time to suggest that nutrient loading is causing a decline in the San Pablo DPS of splittail at the population level now or that it will in the foreseeable future. The known range of the species in the Napa and Petaluma rivers has increased as new surveys have found presence of splittail in areas where they were previously not believed to be found in the mid 1990's

(Sommer et al. 2007, p. 28).

Effects from selenium, mercury, organophosphates, pyrethroids and bioaccumulation on the San Pablo DPS are expected to be comparable to the effects that these potential threats are having on the overall population of splittail. These contaminants are dispersed throughout the estuary and we have no evidence to suggest that there is a higher concentration of these contaminants in the range of the San Pablo DPS than in the entire range of the species. Please refer to Factor E in the range wide analysis for a full discussion of the effects of contaminants on splittail. Based on a review of the best available scientific and commercial data, we conclude that contaminants are not a significant threat to splittail at the population level now or in the foreseeable future.

Climate Change

Climate change is a potential threat to splittail range wide including in the San Pablo Bay and the potential threat of climate change is expected to be the same in scope and intensity as it is in the overall range of the species. Please refer to Factor E in the range wide analysis for a full discussion of the effects of climate change on splittail. Based on a review of the best scientific information available, we find that climate change is not a significant threat to the San Pablo Bay population of splittail now or in the foreseeable future.

Introduced Species

Introduced species are a potential threat to the splittail rangewide and the effects of introduced species on the San Pablo DPS are expected to be similar to the effects on the species range-wide.

However, several introduced species mentioned in the range-wide analysis will not be present in the San Pablo Bay. The invasive Corbula amurensis has become established in San Pablo Bay (USGS 2010); no records exist for Corbicula fluminea, which is physiologically capable of becoming established in the freshwater portions of the Petaluma and

Napa rivers. Corbicula fluminea is not expected to be present in the

San Pablo Bay because it is a

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freshwater clam. Largemouth bass are not expected to be present in San

Pablo Bay because they are a freshwater species.

Brazilian pondweed and water hyacinth are also not expected to be present in this brackish environment because they are freshwater plants. We are lacking any studies on introduced species present in the

Napa and Petaluma rivers. Although the non-native copepods and bivalves discussed in the rangewide analysis have altered the food web in the

Delta ecosystem, we have no compelling evidence to suggest that this has led to a decline in the splittail population. Therefore, we do not consider introduced species to be a significant threat to splittail now or in the foreseeable future.

We conclude that the best scientific and commercial information available indicates that the San Pablo DPS of the Sacramento splittail is not now, nor in the foreseeable future, threatened by other natural or manmade factors affecting its continued existence.

Finding

As required by the Act, we considered the five factors in assessing whether the San Pablo DPS of Sacramento splittail is endangered or threatened. We examined the best scientific and commercial information available regarding the past, present, and future threats faced by the

San Pablo DPS.

The rate of habitat loss in San Pablo Bay that occurred the 1900's is no longer occurring today and efforts undertaken in the past decade have benefited the species by restoring its habitat. There is presently sufficient habitat to maintain the species: inundation frequency and duration in key areas is sufficient to provide spawning to maintain the species. Based on a review of the best scientific information available, we find that the present or threatened destruction, modification, or curtailment of splittail habitat or range (Factor A) is not a significant threat to the San Pablo DPS throughout all or a part of its range.

The new CDFG regulation enacted in March 2010 limiting take of splittail to two individuals per day has eliminated any potential threat that fisheries may have posed. There is no indication that the current level of scientific take adversely affects the San Pablo DPS, and there is no indication that the level of mortality will increase in the future. Based on a review of the best scientific information available, we find that overutilization for commercial, recreational, scientific, or educational purposes (Factor B) is not a significant threat to the San Pablo DPS now or in the foreseeable future.

We found disease occurs at low levels in the population, but does not constitute a significant threat to the species (Factor C).

Predation by striped bass appears to be unchanged from past levels and is currently not a significant threat to the San Pablo DPS. Other freshwater predators are absent from the San Pablo Bay due to elevated salinity levels. Based on a review of the best scientific information available, we find that disease and predation (Factor C) are not significant threats to the San Pablo DPS in all or a significant portion of its range, now or in the foreseeable future.

Federal and State regulations provide protection for the San Pablo

DPS and its habitat by limiting adverse effects from new projects, restoring habitat and limiting contaminants discharged into the

Estuary. Based on a review of the best scientific information, we find that a lack of regulatory mechanisms (Factor D) does not constitute a significant threat to the San Pablo DPS.

Based on the best available science, we find that other natural or manmade factors affecting the continued existence of the San Pablo DPS described in Factor E have not been shown to be significant threats to the San Pablo DPS at this time. Furthermore, there is no compelling evidence to suggest that these factors will increase and become threats to the San Pablo DPS in the foreseeable future. The San Pablo DPS is not threatened by water export facilities, agricultural and power plant diversions, poor water quality, environmental contaminants, climate change, or introduced species (Factor E).

The existing data fails to show a significant long-term decline of the San Pablo DPS. The accepted range of the species in the Napa and

Petaluma rivers has increased as new surveys have found presence of splittail in areas where they were previously not believed to be in the mid-1990's (Sommer et al. 2007, p. 28).Therefore, based on the best available data, we do not find an overall declining trend in the species' population.

Based on our review of the best available scientific and commercial information pertaining to the five factors, we find that the threats are not of sufficient imminence, intensity, or magnitude to indicate that the San Pablo DPS is in danger of extinction (endangered), or likely to become endangered within the foreseeable future (threatened).

Therefore, we find that listing the San Pablo DPS as an endangered or threatened species is not warranted at this time.

Significant Portion of the Range Analysis

Having determined that the splittail does not meet the definition of an endangered or threatened species, we must next consider whether there are any significant portions of the range where the splittail is in danger of extinction or is likely to become endangered in the foreseeable future.

We have analyzed the potential for the San Pablo DPS to make up a significant portion of the species range by looking at areas where there may be a significant concentration of threats. We evaluated the

San Pablo DPS in the context of whether any potential threats are concentrated in one or more areas of the projected range, such that if there were concentrated impacts, those splittail populations might be threatened, and further, whether any such population or complex might constitute a significant portion of the species range. In the case of the San Pablo DPS, we conclude that the potential threats to the species are uniform throughout the DPS. After reviewing the range of the species, we find that no areas have a significant concentration of threats such that a significant portion of the range analysis on them would be necessary.

We do not find that the Sacramento splittail is in danger of extinction now, or is it likely to become endangered within the foreseeable future throughout all or a significant portion of its range. Therefore, listing the Sacramento splittail as endangered or threatened under the Act is not warranted at this time.

We request that you submit any new information concerning the status of, or threats to, the Sacramento splittail or the markedly separate San Pablo DPS to our San Francisco Bay Delta Fish and Wildlife

Office (see ADDRESSES) whenever it becomes available. New information will help us monitor the Sacramento splittail and encourage its conservation. If an emergency situation develops for the splittail or any other species, we will act to provide immediate protection.

References Cited

A complete list of references cited in this finding is available on the Internet at http://www.regulations.gov and upon request from the

San Francisco Bay Delta Fish and Wildlife Office (see ADDRESSES).

Author(s)

The primary authors of this notice are the staff members of the San

Francisco Bay Delta Fish and Wildlife Office, Sacramento, California.

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Authority

The authority for this section is section 4 of the Endangered

Species Act of 1973, as amended (16 U.S.C. 1531 et seq.).

Dated: September 24, 2010

Daniel M. Ashe,

Acting Director, Fish and Wildlife Service.

FR Doc. 2010-24871 Filed 10-6-10; 8:45 am

BILLING CODE 4310-55-S

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