Invasion History

First Non-native North American Tidal Record: 1973
First Non-native West Coast Tidal Record: 1973
First Non-native East/Gulf Coast Tidal Record:

General Invasion History:

Corophium alienense was described from specimens collected in 1973 from San Francisco Bay, California (CA). Based on its recent discovery and its close affinity to many corophiids known from the Northwestern Pacific (Japan, China, Vietnam), it is considered a probable introduction to the Northeastern Pacific. So far, it is known only from San Francisco Bay, Tomales Bay, and Bodega Harbor, CA (Chapman 1988; Cohen and Carlton 1995; Bousfield and Hoover 1997; Fairey et al. 2002).

North American Invasion History:

Invasion History on the West Coast:

Corophium alienense was described from specimens collected in 1973 in Corte Madera Creek, San Quentin, on central San Francisco Bay. The recent discovery of the species, its morphological affinities to Asian corophiids, and its abundance marked it as a probable introduction to San Francisco Bay (Chapman 1988). Within the estuary, it is known from the Central Bay, the South Bay, San Pablo Bay, Carquinez Strait, Grizzly Bay, and Suisun Bay. Peterson and Vayssieres (2010) found that it was abundant in dry years in Grizzly Bay in 1977-1986, but remained abundant and dominant in both dry and wet years in 1987-2003, after the invasion of the Asian Brackish-water Clam Corbula amurensis. Corophium alienense was found to be abundant in Tomales Bay in 1993 (Cohen and Carlton 1995) and was subsequently collected in Tomales Bay in 2011 (California Department of Fish and Wildlife 2014). Chapman (2007) mentions its presence in Los Angeles Harbor, but we have not found any specific records for Southern California. Although C. alienensis probably originated from the coast of Southeast Asia, it has not been reported outside of California (Chapman 1988; Bousfield and Hoover 1997; Chapman 2007).


Description

The estuarine amphipod Corophium alienense is an infaunal amphipod which burrows in muddy sediments. It has a slender, very depressed body, and a massive Antenna 2, which is longer than Antenna 1. The coxal plates are small and separated. The urosome segments are not fused. Both sexes have a pointed rostrum, extending beyond the eye-lobes. The eye is well-developed, but partially obscured by a pigmented cuticle. The first 3 segments of Antenna 1 have long, plumose setae. The 1st segment of the male Antenna 1 lacks a tooth (present in C. heteroceratum). In females, the ventral setae on segments 1-3 are missing. The flagellum has 13-15 segments. Antenna 2 is proportionately larger in males than females, extending well beyond antenna 1. In both sexes, segment 2 bears a large tooth-like excretory spout. In males, segments 4 and 5 of Antenna 2 bear a row of small teeth on the ventral sides. Segment 4 also has a pointed tooth at its distal end. In females, Antenna 2 is only slightly longer than Antenna 1, and lacks the ventral tooth row on segments 4-5, but has a huge distal tooth on segment 4.

The gnathopods are not especially prominent in this genus. Pereiopod 2 is longer than Pereiopod 21 and its dactyl lacks teeth. Pereiopod 7 is nearly twice as long as Pereiopod 6, and has a long curved, smooth, dactyl. The segments of the urosome are separate. Uropod 1 is the longest and 3 is the smallest. The male type specimen was 5.2 mm and the female allotype was 6.4 mm. The centers of the pleonites are mottled brown and white, but the borders, and the appendages are white (photo, in Barnett et al. 2011). Description based on: Chapman 1988, Chapman 2007, and Barnett et al. 2011.

Although C. alienense is known only from San Francisco Bay, Tomales Bay, and Bodega Harbor (Cohen and Carlton 1995; California Department of Fish and Wildlife 2014), it bears a close morphological similarity to Asian species (Chapman 1988; Bousfield and Hoover 1997). Bousfield and Hoover (1997) placed it in the genus Sinocorophium, together with eight Asian species. John Chapman considers the genus Sinocorophium (Bousfield and Hoover 1997) indistinct from Corophium, and thus invalid (Chapman 2007; John Chapman, personal communication).


Taxonomy

Taxonomic Tree

Kingdom:   Animalia
Phylum:   Arthropoda
Subphylum:   Crustacea
Class:   Malacostraca
Subclass:   Eumalacostraca
Superorder:   Peracarida
Order:   Amphipoda
Suborder:   Gammaridea
Family:   Corophiidae
Genus:   Corophium
Species:   alienense

Synonyms

Corophium alienense (Chapman, 1988)
Sinocorophium alienense (Bousfield and Hoover, 1997)
Corophium dentalium (Ren, 1995)

Potentially Misidentified Species

Corophium heteroceratum
Corophium heteroceratum was described from China and has been introduced to San Francisco Bay, Los Angeles-Long Beach Harbor, and Tomales Bay (Cohen and Carlton 1995; Fairey et al. 2002; Chapman 2007).

Ecology

General:

Corophium alienense is a tube-building gammarid amphipod, so far only known from California estuaries (Chapman 1988; Cohen and Carlton 1995; Graening et al. 2012). Gammarid amphipods have separate sexes, brooded embryos, and direct development (Bousfield 1973). We have no specific information on the life history of C. alienense. Nocturnal migration is common in the genus (Chapman 1988).

Corophium alienense is tolerant of a wide range of temperature and salinity, and has been collected in marsh pools at a temperature of 30C (Chapman 2007). It ranges into low-salinity waters in Suisun Bay and the Napa River (Cohen and Carlton 1995; Lee et al. 2003; Peterson and Vaysierres 2010). Corophium alienense builds U-shaped tubes in shallow subtidal and intertidal muddy sand (Chapman 1988; Graening et al. 2012). This amphipod is an abundant member of the epifauna on Eelgrass (Zostera marina) in San Francisco Bay (Carr et al. 2011). Corophium alienense is a suspension-feeder, and surface-deposit-feeder. It is considered a significant grazer in brackish tributaries of San Francisco Bay (Jones et al. 2009; Barnett et al. 2011). Fishes are the primary predators of benthic amphipods in these estuaries (Feyrer et al. 2003).

Food:

Detritus; Phytyoplankton

Trophic Status:

Deposit Suspension Feeder

DepSusFed

Habitats

General HabitatUnstructured BottomNone
General HabitatGrass BedNone
Salinity RangeLimnetic0-0.5 PSU
Salinity RangeOligohaline0.5-5 PSU
Salinity RangeMesohaline5-18 PSU
Salinity RangePolyhaline18-30 PSU
Tidal RangeSubtidalNone
Vertical HabitatEpibenthicNone
Vertical HabitatEndobenthicNone

Life History


Tolerances and Life History Parameters

Minimum Temperature (ºC)30Field (Chapman 2007)
Minimum Salinity (‰)0.7Field, mean salinity, Fresh-Brackish-Muddy zone, San Francisco Delta (Lee et al. 2003)
Maximum Salinity (‰)27.5Field, mean salinity, Marine-Muddy zone, South and Central San Francisco Bay (Lee et al. 2003)
Maximum Length (mm)6.4Adult female (Chapman 1988)
Broad Temperature RangeNoneWarm temperate
Broad Salinity RangeNoneTidal Limnetic-Polyhaline

General Impacts

Corophium alienense is one of the dominant benthic organisms in brackish tributaries of San Francisco Bay. It increased in abundance after the invasion of the Asian Brackish-water Clam (Corbula amurensis) (Peterson and Vayssieres 2010). In Suisun Slough, the estimated grazing rate of C. alienense was ~15X greater than that of C. amurensis. However, the rate of phytoplankton loss due to grazing was much smaller than the loss by sedimentation, which was attributed to a flocculent surface layer of mucus, to which the tubes of C. alienense contributed, along with many other benthic organisms (Jones et al. 2009). Tube-building amphipods, including C. alienense, are important food items for native and introduced benthic-feeding fishes in San Francisco Bay (Feyrer et al. 2003).


Regional Impacts

NEP-VNorthern California to Mid Channel IslandsEcological ImpactHabitat Change
In Suisun Slough, mucus from the tubes of C. alienense as well as the mucus produced by other native and introduced deposit feeding and tube-building benthos, contributes to a surface layer of flocculent fluff, which may trap much more phytoplankton than that actually consumed by the animals (Jones et al. 2009).
P090San Francisco BayEcological ImpactHabitat Change
In Suisun Slough, mucus from the tubes of C. alienense as well as the mucus produced by other native and introduced deposit feeding and tube-building benthos, contributes to a surface layer of flocculent fluff, which may trap much more phytoplankton than that actually consumed by the animals (Jones et al. 2009).
P090San Francisco BayEcological ImpactHerbivory
Corophium alienense is a significant suspension-feeder in the benthos of Suisun Slough, and other brackish San Francisco Bay tributaries. Specific grazing rates for the population were estimated from those of the similar Atlantic amphipod C. volutator, as 9 m-3 . m-2 . day-1, for the populaiton about 15X higher than that of the Asian Brackish-Water Clam ( Corbula amurensis) population (Jones et al. 2009). This estimate makes it the major suspension-feeder in this part of the San Francisco estuary.
NEP-VNorthern California to Mid Channel IslandsEcological ImpactHerbivory
Corophium alienense is a significant suspension-feeder in the benthos of Suisun Slough, and other brackish San Francisco Bay tributaries. Specific grazing rates for the population were estimated from those of the similar Atlantic amphipod C. volutator, as 9 m-3 . m-2 . day-1, for the populaiton about 15X higher than that of the Asian Brackish-Water Clam (Corbula amurensis) population (Jones et al. 2009). This estimate makes it the major suspension-feeder in this part of the San Francisco estuary.
P090San Francisco BayEcological ImpactFood/Prey
Tube-dwelling and free-living gammarid amphipods were important food items for several native (Tule Perch- Hysterocarpus traskii, Prickly Sculpin- Cottus asper, Starry Flounder- Platichthys stellatus) and introduced fishes (Acanthogobius longimanus, Yellowfin Goby) (Feyrer et al. 2003).
NEP-VNorthern California to Mid Channel IslandsEcological ImpactFood/Prey
Tube-dwelling and free-living gammarid amphipods were important food items for several native (Tule Perch- Hysterocarpus traskii, Prickly Sculpin- Cottus asper, Starry Flounder- Platichthys stellatus) and introduced fishes (Acanthogobius longimanus, Yellowfin Goby) (Feyrer et al. 2003).
CACaliforniaEcological ImpactFood/Prey
Tube-dwelling and free-living gammarid amphipods were important food items for several native (Tule Perch- Hysterocarpus traskii, Prickly Sculpin- Cottus asper, Starry Flounder- Platichthys stellatus) and introduced fishes (Acanthogobius longimanus, Yellowfin Goby) (Feyrer et al. 2003)., Tube-dwelling and free-living gammarid amphipods were important food items for several native (Tule Perch- Hysterocarpus traskii, Prickly Sculpin- Cottus asper, Starry Flounder- Platichthys stellatus) and introduced fishes (Acanthogobius longimanus, Yellowfin Goby) (Feyrer et al. 2003).
CACaliforniaEcological ImpactHabitat Change
In Suisun Slough, mucus from the tubes of C. alienense as well as the mucus produced by other native and introduced deposit feeding and tube-building benthos, contributes to a surface layer of flocculent fluff, which may trap much more phytoplankton than that actually consumed by the animals (Jones et al. 2009)., In Suisun Slough, mucus from the tubes of C. alienense as well as the mucus produced by other native and introduced deposit feeding and tube-building benthos, contributes to a surface layer of flocculent fluff, which may trap much more phytoplankton than that actually consumed by the animals (Jones et al. 2009).
CACaliforniaEcological ImpactHerbivory
Corophium alienense is a significant suspension-feeder in the benthos of Suisun Slough, and other brackish San Francisco Bay tributaries. Specific grazing rates for the population were estimated from those of the similar Atlantic amphipod C. volutator, as 9 m-3 . m-2 . day-1, for the populaiton about 15X higher than that of the Asian Brackish-Water Clam (Corbula amurensis) population (Jones et al. 2009). This estimate makes it the major suspension-feeder in this part of the San Francisco estuary., Corophium alienense is a significant suspension-feeder in the benthos of Suisun Slough, and other brackish San Francisco Bay tributaries. Specific grazing rates for the population were estimated from those of the similar Atlantic amphipod C. volutator, as 9 m-3 . m-2 . day-1, for the populaiton about 15X higher than that of the Asian Brackish-Water Clam ( Corbula amurensis) population (Jones et al. 2009). This estimate makes it the major suspension-feeder in this part of the San Francisco estuary.

Regional Distribution Map

Bioregion Region Name Year Invasion Status Population Status
P110 Tomales Bay 2011 Def Estab
NEP-VI Pt. Conception to Southern Baja California 2007 Def Estab
P050 San Pedro Bay 2007 Def Estab
P112 _CDA_P112 (Bodega Bay) 1992 Def Estab
NEP-V Northern California to Mid Channel Islands 1973 Def Estab
P090 San Francisco Bay 1973 Def Estab
P093 _CDA_P093 (San Pablo Bay) 1973 Def Estab

Occurrence Map

OCC_ID Author Year Date Locality Status Latitude Longitude
755433 Introduced Species Study 2005 2005-10-07 Martinez Marina Def 38.0276 -122.1371
755434 Introduced Species Study 2005 2005-10-19 Rodeo Marina Def 38.0394 -122.2717
755435 Introduced Species Study 2010 2010-05-31 Dumbarton Bridge Def 37.5070 -122.1168
755436 Introduced Species Study 2010 2010-05-31 Redwood Creek - Marina Def 37.5021 -122.2130
755437 Introduced Species Study 2010 2010-05-31 Redwood Creek - Shipping Def 37.5120 -122.2109
755438 Introduced Species Study 2010 2010-06-01 Coyote Point Marina Def 37.5905 -122.3177
755439 Introduced Species Study 2010 2010-06-01 Sea Plane Harbor Def 37.6349 -122.3848
755440 Introduced Species Study 2010 2010-06-02 Ballena Bay Def 37.7661 -122.2834
755441 Introduced Species Study 2010 2010-06-02 Coast Guard Island Def 37.7812 -122.2457
755442 Introduced Species Study 2010 2010-06-02 Port of Oakland Office Def 37.7954 -122.2804
755443 Introduced Species Study 2010 2010-06-13 Hayward Landing Def 37.6447 -122.1543
755444 Introduced Species Study 2010 2010-06-28 Chevron Pier Def 37.9228 -122.4105
755445 Introduced Species Study 2010 2010-06-28 Point Richmond Piers Def 37.9085 -122.3913
755446 Introduced Species Study 2010 2010-06-29 New York Point Marina Def 38.0400 -121.8863
755447 Introduced Species Study 2010 2010-07-01 Ayala Cove Def 37.8680 -122.4350
755448 Introduced Species Study 2010 2010-07-12 Ferry Terminal Pier Def 37.7945 -122.3917
755449 Introduced Species Study 2010 2010-07-15 San Pablo Bay Pumphouse Def 38.0446 -122.4326
755450 Introduced Species Study 2010 2010-07-29 Mare Island Strait - Navy Def 38.1015 -122.2695
755451 Introduced Species Study 2011 2011-06-06 Tomales Bay Boat Launch Def 38.1991 -122.9220
758364 J. Chapman, pers. comm., in Carlton 1979 1970 San Francisco Bay Def 37.8494 -122.3681
758365 Chapman 1988 1973 Corte Madera, SE of San Quentin Prison Def 37.9367 -122.4871
758366 Chapman 1988 1973 Mare Island Channel Def 38.0954 -122.2612
758367 Chapman 1988 1976 1976-08-27 Coyote Creek, immediately south of the Southern Pacific Railroad Bridge Def 37.4606 -121.9748
758368 Chapman 1988 1973 Carquinez Strait, near Benicia Municipal Pier Def 38.0409 -122.1739
758369 Thompson and Nichols 1984; Chapman 1988 1974 1974-12-10 Sand Point, Palo Alto (USGS Station 45) Def 37.4630 -122.1011
758370 W.C. Fields, pers. comm., in Chapman 1988 1980 Delta General Location Def 38.0500 -121.8100
758371 Chapman 1988 1980 Grizzly Island Def 38.1485 -121.9819
758372 J. Chapman, pers. comm., in Cohen and Carlton 1995 1992 Bodega Harbor Def 38.3262 -123.0495
758373 Cohen and Carlton 1995 1993 Tiburon, San Francisco Bay Def 37.8881 -122.4803
758374 Cohen and Carlton 1995 1993 Napa River, San Pablo Bay Def 38.1402 -122.2764
758375 Cohen and Carlton 1995 1993 Rodeo, San Pablo Bay Def 38.0394 -122.2749
758376 Cohen and Carlton 1995 1994 Tiburon, San Francisco Bay Def 37.8881 -122.4803
758377 Cohen and Carlton 1995 1994 Napa River, San Pablo Bay Def 38.1402 -122.2764
758378 Cohen and Carlton 1995 1994 Rodeo, San Pablo Bay Def 38.0394 -122.2749
758379 Cohen et al. 2005 (SF Bay Area RAS) 2004 2004-05-28 Rodeo Marina, San Pablo Bay Def 38.0391 -122.2711
820043 Ruiz GM and JB Geller (2018) 2015 Oakland None 37.7056 -122.2473
820044 Ruiz GM and JB Geller (2018) 2015 Ballena Isle None 37.7588 -122.2834
820045 Ruiz GM and JB Geller (2018) 2015 SF marina None 37.8074 -122.4345
820046 Ruiz GM and JB Geller (2018) 2015 Richardson bay None 37.8705 -122.4797
820047 Ruiz GM and JB Geller (2018) 2015 Smithsonian None 37.8981 -122.4623
820048 Ruiz GM and JB Geller (2018) 2015 Hunters Point None 37.7088 -122.3691
820049 Ruiz GM and JB Geller (2018) 2015 Oyster Point None 37.6747 -122.3753
820050 Ruiz GM and JB Geller (2018) 2015 Union City None 37.5865 -122.1743
820051 Ruiz GM and JB Geller (2018) 2015 Albany None 37.8879 -122.3245
820052 Ruiz GM and JB Geller (2018) 2015 San Lorenzo None 37.6480 -122.2159
820253 Ruiz GM and JB Geller (2018) 2016 SF marina None 37.8071 -122.4345
820254 Ruiz GM and JB Geller (2018) 2016 Bay Farm None 37.7237 -122.2632
820255 Ruiz GM and JB Geller (2018) 2016 Brisbane None 37.6560 -122.3697
820256 Ruiz GM and JB Geller (2018) 2016 Mission Bay None 37.7553 -122.3790
820257 Ruiz GM and JB Geller (2018) 2016 Albany None 37.8773 -122.3241
820258 Ruiz GM and JB Geller (2018) 2016 El Cerrito None 37.8885 -122.3367
820259 Ruiz GM and JB Geller (2018) 2016 Richardson bay None 37.8669 -122.4751
820260 Ruiz GM and JB Geller (2018) 2016 Paradise Cay None 37.9044 -122.4684
820261 Ruiz GM and JB Geller (2018) 2016 Oyster Point None 37.6688 -122.3741
820262 Ruiz GM and JB Geller (2018) 2016 Ballena Isle None 37.7516 -122.2878

References

Barnett, Rachel; Bell, Sabrina; Floerke, Wyatt; Templin, Bill (2011) <missing title>, California Interagency Ecological Program, Sacramento CA. Pp. 13

Bousfield, E. L.; Hoover, P. M. (1997) The amphipod superfamily Corophioidea on the Pacific coast of North America. Part V. Family Corophiidae: Corophiinae, new subfamily. Systematics and distributional ecology., Amphipacifica 2(3): 67-139

Bousfield, E.L. (1973) <missing title>, Comstock Publishing Associates, Ithaca, NY. Pp. <missing location>

California Department of Fish and Wildlife (2014) Introduced Aquatic Species in California Bays and Harbors, 2011 Survey, California Department of Fish and Wildlife, Sacramento CA. Pp. 1-36

Carr, Lindsey A.; Boyer, Katharyn E.; Brooks, Andrew J. (2011) Spatial patterns of epifaunal communities in San Francisco Bay eelgrass (Zostera marina) beds, Marine Ecology 32: 88-103

Chapman, John W. (1988) Invasions of the Northeast Pacific by Asian and Atlantic Gammaridean amphipod crustaceans, including a new species of Corophium, Journal of Crustacean Biology 8(3): 364-382

Chapman, John W. (2007) The Light and Smith Manual: Intertidal invertebrates from Central California to Oregon (4th edition), University of California Press, Berkeley CA. Pp. 545-611

Cohen, Andrew N.; Carlton, James T. (1995) Nonindigenous aquatic species in a United States estuary: a case study of the biological invasions of the San Francisco Bay and Delta, U.S. Fish and Wildlife Service and National Sea Grant College Program (Connecticut Sea Grant), Washington DC, Silver Spring MD.. Pp. <missing location>

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Graening, G. O.; Rogers, D. Christopher; Holsinger, John R.; Barr, Cheryl; Bottorff, Richard (2012) Checklist of inland aquatic Amphipoda (Crustacea: Malacostraca) of California, Zootaxa 3544: 1-27

Howe, Emily R.; Simenstad, Charles A.; Toft, Jason D.; Cordell, Jeffrey R.; Bollens, Stephen M. (2014) Macroinvertebrate prey availability and fish diet selectivity in relation to environmental variables in natural and restoring North San Francisco Bay tidal marsh channels, San Francisco Estuary and Watershed Science 12(1): 1-46

Jones, Nicole L.; Thompson, Janet K.; Arrigo, Kevin R.; Monismith, Stephen G. (2009) Hydrodynamic control of phytoplankton loss to the benthos in an estuarine environment, Limnology and Oceanography 54(3): 952-969

Lee, Henry II; Thompson, Bruce; Lowe, Sarah (2003) Estuarine and scalar patterns of invasion in the soft-bottom benthic communities of the San Francisco estuary., Biological Invasions 5: 85-102

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