Invasion History

First Non-native North American Tidal Record: 1907
First Non-native West Coast Tidal Record: 1907
First Non-native East/Gulf Coast Tidal Record:

General Invasion History:

Tritia obsoleta is native to the Northwest Atlantic, from the Bay of Chaleur, Quebec, in the Gulf of Saint Lawrence to western Florida (Bousfield 1960; Abbott 1974). It was first collected in San Francisco Bay in 1907, where it was introduced with Eastern Oysters (Dall 1907, cited by Carlton 1979) and is now widespread and abundant (Cohen and Carlton 1995; Cohen et al. 2005). It was also introduced to Willapa Bay, Washington and Boundary Bay, British Columbia by 1945 and 1952, respectively. It is established in both bays (Carlton 1979; Wonham and Carlton 2005).

North American Invasion History:

Invasion History on the West Coast:

Tritia obsoleta was first found in beds of newly planted Eastern Oysters (Crassostrea virginica) at Alameda, in San Francisco Bay by W. H. Dall in 1907 (Carlton 1979). It is now the most abundant gastropod on mudflats in San Francisco Bay. It ranges throughout the South and Central bays, and through San Pablo Bay to the Carquinez Straits (Carlton 1979; Nichols and Thompson 1985; Cohen and Carlton 1995; California Academy of Sciences 2008). In San Pablo Bay, it was found at sites from 9.5 to 25 PSU (Filice 1959, cited by Carlton 1979). Surprisingly, this snail has been collected in other California estuaries, but has not become established. Locations (listed from South to North) include: Monterey Bay, Moss Landing Harbor in 1971 (California Academy of Sciences 2008); Bolinas Lagoon in 1925 (Carlton 1979), Tomales Bay in 1930 (MacGinitie 1930, cited by Carlton 1979); Bodega Harbor in 1968 (Carlton 1979), and Humboldt Bay in 1932 (failed, Hanna 1966, Carlton 1979).

Tritia obsoleta was first collected in Willapa Bay, Washington (WA) and Boundary Bay, British Columbia in 1945 and 1952, respectively, but may have been introduced much earlier (1874-1905) with early oyster plantings. Collecting in these areas was sparse in the early 20th century (Carlton 1979). This snail is locally abundant in both bays (Cohen et al. 200; Sakamaki and Richardson 2006), but it has not been reported from Puget Sound, WA or from other locations in British Columbia (Cohen et al. 1998; Gillespie et al. 2007).


Description

Ilyanassa obsoleta (Eastern Mud Snail) is a medium-sized marine and estuarine snail. Its shell is oval, and dextrally coiled, with a well-defined spire, usually eroded at the tip. The adult shell has 6-7 whorls. The parietal wall (inner lip) is thick and glazed with brown and gray. The columella has a spiral ridge near the base. The shell is weakly sculpted with numerous rows of small beads, running roughly at right angles to the growth lines. The outer lip has six small grayish teeth. The shell reaches 25-30 mm. The color of the shell is dark blackish-brown, often overgrown with algae or smeared with mud. The name Ilyanassa obsoleta is widely used, but a molecular analysis found that no genetic distinction between the genera Ilyanassa, Cyclope, and Tritia (Galindo et al. 2016). However, a later analysis restored the distinctness of the genus Ilyanassa (Yang et al. 2021). Escription from: Abbott 1974; Morris 1975; Gosner 1978; and McLean, in Carlton 2007.

Larval development of T. obsoleta is illustrated by Scheltema (1962).


Taxonomy

Taxonomic Tree

Kingdom:   Animalia
Phylum:   Mollusca
Class:   Gastropoda
Subclass:   Prosobranchia
Order:   Neogastropoda
Family:   Nassariidae
Species:   obsoleta

Synonyms

Buccinum noveboracense (Wood, 1828)
Buccinum oliviforme (Kiener, 1834)
Ilyanassa obsoleta (Stimpson, 1865)
Nassa obsoleta (Say, 1822)
Nassarius obsoletus (None, None)
Tritia obsoleta (Galindo et al., 2016)
Ilyanassa obsoleta (Yi et al., 2021)

Potentially Misidentified Species

Caesia fossata
Commonly known as the Giant Western Nassa, native to the West Coast from Vancouver Island to Baja California. Larger, more sculptured, notch between end of columella and outer lip (Abbott 1974, McLean in Carlton 2007).

Ecology

General:

Ilyanassa obsoleta is an estuarine-marine snail, especially associated with mudflats and other soft-sediment habitats. Sexes are separate and animals mature at about 12-14 mm, which in Massachusetts populations is reached in their third summer (Scheltema 1964). Fertilization is internal and eggs are laid in capsules, about 2.7 mm in height, containing about 40-150 eggs (Scheltema 1962). Small, medium, and large females laid means of 31, 55, and 79 egg capsules, respectively (Schwab 2012). The straw-colored capsules are distinctive, armed with spiny flanges, and are attached to the substrate. The eggs hatch into planktotrophic veligers, which take 10-22 days to develop at 17.5 to 25°C. The veligers settle and metamorphose at about 650-750 µm (Scheltema 1962).

Ilyanassa obsoleta spends much of its time on exposed intertidal mudflats where it experiences a wide range of temperatures and salinities. It tolerates temperatures as high as 30°C in water (Vernberg and Vernberg 1969) and probably higher in air when exposed. This snail responds to winter cold by migrating into shallow subtidal waters (Batchelder 1915: Murphy 1979). It tolerates salinities as low as 10 PSU (Carlton 1979; Cohen et al. 2001) and at least as high as 35 PSU, near the ocean, and maybe higher in salt marsh pools. The temperature range for larval development is 16.5 to 28°C and the salinity range is 21-33 (highest tested) PSU (Scheltema 1965).

Ilyanassa obsoleta is an omnivore. Young snails in aquaria graze on algae growing on glass and probably feed by this method in the wild. As they grow, they switch to ingesting large quantities of sediment, together with organic matter and benthic diatoms. They also feed on decaying algae, such as Ulva, and are strongly attracted to carrion, such as dead fish and mollusks. However, they do not attack or feed on living bivalves (Scheltema 1964). This snail is eaten by fishes, crabs, and birds. It is also a host to many species of parasites. Blakeslee et al. (2012) found nine species of trematodes in I obsoleta from its native range, four each with birds or fishes as final hosts, and one infecting a turtle (Diamondback Terrapin, Malaclemys terrapin). Four of these parasites were found in I. obsoleta on the West Coast. (See 'Impacts' section for details.)

Food:

Detritus, Carrion, Algae

Consumers:

Fish, crabs, birds

Competitors:

Littorina littorea

Trophic Status:

Omnivore

Omni

Habitats

General HabitatUnstructured BottomNone
General HabitatOyster ReefNone
General HabitatSalt-brackish marshNone
Salinity RangeMesohaline5-18 PSU
Salinity RangePolyhaline18-30 PSU
Salinity RangeEuhaline30-40 PSU
Tidal RangeSubtidalNone
Tidal RangeLow IntertidalNone
Tidal RangeMid IntertidalNone
Vertical HabitatEpibenthicNone


Tolerances and Life History Parameters

Minimum Temperature (ºC)0Experimental, limited winter freezing tolerance, response to cold by migrating to deeper water(Murphy 1979)
Maximum Temperature (ºC)30Snails from North Carolina were acclimated at this temperature. A temperature of 37 C resulted in ~50% mortality in 6 hours for unparasitized snails (Vernberg and Vernberg (1969).
Minimum Salinity (‰)10Field and Experimental, inactivity in adults inhibited below 12.5 PSU (Scheltema 1965). But animals abundant at 9-10 PSU (Carlton 1979; Cohen et al. 2001).
Maximum Salinity (‰)35Typical ocean salinity, probably experiences higher salinities in marsh and mudflat pools.
Minimum Reproductive Temperature16.5Temperature for larval development, experimental. No development at 11.5 C. Scheltema 1967)
Maximum Reproductive Temperature28Temperature for larval development, experimental, highest tested (Scheltema 1967)
Minimum Reproductive Salinity20.9Minimum salinity for completion of metamorphosis, not completed at 17.1 ppt (Scheltema 1965)
Minimum Duration10Experimental, larval duration, 25.2 C, beginning of creeping-swimming period (Scheltema 1967)
Maximum Duration22Experimental, larval duration,17.5 C, beginning of creeping-swimming period (Scheltema 1967)
Minimum Length (mm)14Size at maturity (Scheltema 1964)
Maximum Length (mm)30Shells in San Francisco Bay often reach 30 mm (Carlton 1979) but the usually reported maximum for the East Coast is 25 mm (Abbott 1974; Morris 1975).
Broad Temperature RangeNoneCold temperate-Warm temperate
Broad Salinity RangeNoneMesohaline-Euhaline

General Impacts

Tritia obsoleta has developed dense populations on the West Coast. The ecology of this species has been extensively studied on the East Coast, but much less is known about the ecology and impacts of this species on the West Coast. In San Francisco Bay (California), it has displaced the native California Hornshell (Cerithidea californica) from many habitats. In Willapa (Washington) and Boundary Bays (WA/British Columbia), where there are dense populations, and no native equivalents, it may have affected sediment characteristics and foodwebs. However, these impacts have not been studied. The introduction of T. obsoleta resulted in the transport of five digenetic trematode species to San Francisco Bay. Three of these parasites reached Willapa Bay, and two reached Boundary Bay. The adult hosts of these parasites are birds and fishes, but the effects of these parasites on the hosts are not known (Blakeslee et al. 2012).

Economic Impacts

Health: Outbreaks of 'Swimmers Itch' in San Francisco Bay were traced to the cercaria larvae of a blood-fluke (schistosome), Austrobilharzia variglandis, whose intermediate host is Tritia obsoleta. The final host of the trematode is birds, but the cercaria frequently penetrate the skin of bathing humans, where they cannot develop, but do cause itching and irritation. The trematode is believed to have been introduced to the San Francisco Bay with T. obsoleta (Grodhaus and Keh 1958).

Ecological Impacts

Competition: In San Francisco Bay, Tritia obsoleta has displaced the native snail Cerithidea californica (California Hornsnail) in tidal creeks and restricted them to salt pans (i.e. habitats with higher temperatures and more desiccation). These conditions are beyond the tolerance of T. obsoleta, but are tolerated (but are perhaps suboptimal) by C. californica. The mechanism of competition appears to be behavioral interference, in which T. obsoleta move over and bump into C. californica. The native snails respond by withdrawing into their shells, reducing the time available for foraging (Race 1982).

Predation: Tritia obsoleta has reduced recruitment of Cerithidea californica (California Hornsnail) in San Francisco Bay, by consuming C. californica's egg capsules (Race 1982).

Parasite/Predator Vector: The introduction of T. obsoleta resulted in the transport of five digenetic trematode species to the West Coast: Zoogonus lasius (as Z. rubellus); Lepocreadium setiferoides; Stephanostomum tenue; Himasthla quissetensis; and Austrobilharzia variglandis. The first three of these species have fishes as final hosts; the last two have birds (shorebirds, gulls, cormorants, ducks) as final hosts (Blakeslee et al. 2012). All of these parasites are present in San Francisco Bay, while three were found in Willapa Bay, and two in Boundary Bay. The two most widespread parasites, H. quissetensis and A. variglandis are bird-hosted as adults. Impacts of these parasites on their final hosts is unknown.

Regional Impacts

NEP-VNorthern California to Mid Channel IslandsEcological ImpactCompetition
Tritia obsoleta has displaced the native snail Cerithidea californica in San Francisco Bay from tidal creeks. The native snails actively withdraw from T. obsoleta, and are mostly restricted to salt pans, which are frequently subject to high temperatures and desiccation (Race 1982).
NEP-VNorthern California to Mid Channel IslandsEcological ImpactPredation
Tritia obsoleta actively feeds on the egg capsules of the native snail Cerithidea californica in San Francisco Bay (Race 1982)
P090San Francisco BayEcological ImpactCompetition
Tritia obsoleta has displaced the native snail Cerithidea californica in San Francisco Bay from tidal creeks. The native snails actively withdraw from T. obsoleta, and are mostly restricted to salt pans, which are frequently subject to high temperatures and desiccation (Race 1982).
P090San Francisco BayEcological ImpactPredation
Tritia obsoleta actively feeds on the egg capsules of the native snail Cerithidea californica in San Francisco Bay (Race 1982)
NEP-VNorthern California to Mid Channel IslandsEcological ImpactParasite/Predator Vector
The introduction of T. obsoleta resulted in the transport of 5 digenetic trematode species to San Francisco Bay: Zoogonus lasius (as Z. rubellus); Lepocreadium setiferoides; Stephanostomum tenue; Himasthla quissetensis; Austrobilharzia variglandis. The first 3 of these species have fishes as final hosts; the last 2 have birds (shorebirds, gulls, cormorants, ducks) as final hosts (Blakeslee et al. 2012). The effect of these parasites on their final hosts is unknown.
P090San Francisco BayEcological ImpactParasite/Predator Vector
The introduction of T. obsoleta resulted in the transport of 5 digenetic trematode species to San Francisco Bay: Zoogonus lasius (as Z. rubellus); Lepocreadium setiferoides; Stephanostomum tenue; Himasthla quissetensis; Austrobilharzia variglandis. The first 3 of these species have fishes as final hosts; the last 2 have birds (shorebirds, gulls, cormorants, ducks) as final hosts (Blakeslee et al. 2012). The effect of these parasites on their final hosts is unknown.
NEP-IVPuget Sound to Northern CaliforniaEcological ImpactPredation
The introduction of T. obsoleta resulted in the transport of 3 digenetic trematode species to Willapa Bay: Zoogonus lasius (as Z. rubellus); Himasthla quissetensis; Austrobilharzia variglandis. The first of these species has fishes as its final hosts; the last 2 have birds (shorebirds, gulls, cormorants, ducks) as final hosts (Blakeslee et al. 2012). The effect of these parasites on their final hosts is unknown.
P090San Francisco BayEconomic ImpactHealth
Tritia obsoleta is an intermediate host of the digenetic trematode (blood-fluke, schistosome) Austrobilharzia variglandis. The final host of the the trematode is birds but the cercaria frequently infect the skin of bathing humans, causing Swimmer's Itch (Grodhaus and Keh 1958).
NEP-VNorthern California to Mid Channel IslandsEconomic ImpactHealth
Tritia obsoleta is an intermediate host of the digenetic trematode (blood-fluke, schistosome) Austrobilharzia variglandis. The final host of the trematode is birds, but the cercaria frequently infect the skin of bathing humans, causing Swimmer's Itch (Grodhaus and Keh 1958).
CACaliforniaEcological ImpactCompetition
Tritia obsoleta has displaced the native snail Cerithidea californica in San Francisco Bay from tidal creeks. The native snails actively withdraw from T. obsoleta, and are mostly restricted to salt pans, which are frequently subject to high temperatures and desiccation (Race 1982)., Tritia obsoleta has displaced the native snail Cerithidea californica in San Francisco Bay from tidal creeks. The native snails actively withdraw from T. obsoleta, and are mostly restricted to salt pans, which are frequently subject to high temperatures and desiccation (Race 1982).
CACaliforniaEcological ImpactParasite/Predator Vector
The introduction of T. obsoleta resulted in the transport of 5 digenetic trematode species to San Francisco Bay: Zoogonus lasius (as Z. rubellus); Lepocreadium setiferoides; Stephanostomum tenue; Himasthla quissetensis; Austrobilharzia variglandis. The first 3 of these species have fishes as final hosts; the last 2 have birds (shorebirds, gulls, cormorants, ducks) as final hosts (Blakeslee et al. 2012). The effect of these parasites on their final hosts is unknown., The introduction of T. obsoleta resulted in the transport of 5 digenetic trematode species to San Francisco Bay: Zoogonus lasius (as Z. rubellus); Lepocreadium setiferoides; Stephanostomum tenue; Himasthla quissetensis; Austrobilharzia variglandis. The first 3 of these species have fishes as final hosts; the last 2 have birds (shorebirds, gulls, cormorants, ducks) as final hosts (Blakeslee et al. 2012). The effect of these parasites on their final hosts is unknown.
CACaliforniaEcological ImpactPredation
Tritia obsoleta actively feeds on the egg capsules of the native snail Cerithidea californica in San Francisco Bay (Race 1982), Tritia obsoleta actively feeds on the egg capsules of the native snail Cerithidea californica in San Francisco Bay (Race 1982)
CACaliforniaEconomic ImpactHealth
Tritia obsoleta is an intermediate host of the digenetic trematode (blood-fluke, schistosome) Austrobilharzia variglandis. The final host of the trematode is birds, but the cercaria frequently infect the skin of bathing humans, causing Swimmer's Itch (Grodhaus and Keh 1958)., Tritia obsoleta is an intermediate host of the digenetic trematode (blood-fluke, schistosome) Austrobilharzia variglandis. The final host of the the trematode is birds but the cercaria frequently infect the skin of bathing humans, causing Swimmer's Itch (Grodhaus and Keh 1958).

Regional Distribution Map

Bioregion Region Name Year Invasion Status Population Status
P080 Monterey Bay 1971 Non-native Failed
P112 _CDA_P112 (Bodega Bay) 1968 Non-native Failed
NEP-IV Puget Sound to Northern California 1945 Non-native Established
P130 Humboldt Bay 1932 Non-native Failed
P110 Tomales Bay 1930 Non-native Failed
P095 _CDA_P095 (Tomales-Drakes Bay) 1925 Non-native Failed
P093 _CDA_P093 (San Pablo Bay) 1907 Non-native Established
NEP-V Northern California to Mid Channel Islands 1907 Non-native Established
P090 San Francisco Bay 1907 Non-native Established

Occurrence Map

OCC_ID Author Year Date Locality Status Latitude Longitude
714359 Hanna 1966; Carlton 1979 1920 Tomales Bay Non-native 38.1697 -122.9089
714361 Hanna 1966; Carlton 1979 1930 Humboldt Bay Non-native 40.7500 -124.2083
714362 Carlton 1979 1968 Bodega Harbor Non-native 38.3130 -123.0600
714363 Cohen and Carlton 1995 1995 Alameda Non-native 37.7521 -122.2643
714364 Thompson and Nichols 1984; Nichols and Thompson 1985b 1984 Sand Point, Palo Alto Non-native 37.4630 -122.1011
714716 California Academy of Sciences Invertebrate Zoology Collections Database 1975 1975-12-28 Pinole Point Non-native 38.0128 -122.3656
714717 California Academy of Sciences Invertebrate Zoology Collections Database 1977 1977-02-02 Cooley Landing, south of jetty Non-native 37.4752 -122.1203
714718 California Academy of Sciences Invertebrate Zoology Collections Database 1973 1973-03-14 Carquinez Strait Disposal Site Non-native 38.0636 -122.2639
714719 California Academy of Sciences Invertebrate Zoology Collections Database 1973 1973-03-07 Redwood City Harbor Entrance Channel Non-native 37.5405 -122.1936
714720 California Academy of Sciences Invertebrate Zoology Collections Database 1976 1976-08-26 Coyote Hills Slough (at mouth) Non-native 37.5633 -122.1309
714721 California Academy of Sciences Invertebrate Zoology Collections Database 1977 1977-08-16 Ravenswood Slough, at mouth Non-native 37.5000 -122.1582
714722 Filice 1954_; Hopkins 1986 1951 1951-10-06 Carquinez Strait, NW of Davis Point Non-native 38.0492 -122.2644
714723 California Academy of Sciences Invertebrate Zoology Collections Database 1978 1978-06-21 India Basin (Station C-3-2) Non-native 37.7361 -122.3694
714724 California Academy of Sciences Invertebrate Zoology Collections Database 1973 1973-12-17 Mare Island Strait Non-native 38.0997 -122.2647
714725 California Academy of Sciences Invertebrate Zoology Collections Database 1989 Hoffman Marsh, Richmond Non-native 37.9041 -122.3186
714729 California Academy of Sciences Invertebrate Zoology Collections Database 1922 1922-08-28 Dumbarton Bridge Non-native 37.5053 -122.1183
714730 California Academy of Sciences Invertebrate Zoology Collections Database 1955 Palo Alto Yacht Harbor Non-native 37.4584 -122.1052
714731 California Academy of Sciences Invertebrate Zoology Collections Database None Near Key Route Pier, Oakland Non-native 37.8182 -122.3441
714732 Filice 1958 1951 1951-11-10 Martinez Yacht Harbor Non-native 38.0272 -122.1361
714733 California Academy of Sciences Invertebrate Zoology Collections Database 1976 1976-01-24 Newark Slough (at mouth) Non-native 37.5062 -122.0857
714734 California Academy of Sciences Invertebrate Zoology Collections Database 1972 1972-09-14 off Fremont, near Channel Marker 18 Non-native 37.4692 -122.0617
714735 California Academy of Sciences Invertebrate Zoology Collections Database 1970 1970-08-13 San Rafael Bay Non-native 37.9639 -122.4764
714736 California Academy of Sciences Invertebrate Zoology Collections Database 1984 1984-10-25 Selby Non-native 38.0590 -122.2414
714737 California Academy of Sciences Invertebrate Zoology Collections Database 1981 1981-08-04 Lower Steamboat Slough Non-native 38.2141 -122.4278
714738 California Academy of Sciences Invertebrate Zoology Collections Database 1971 1971-11-30 Moss Landing Non-native 36.8036 -121.7854
714962 Gilmore 1935, cited in Carlton 1979 1935 Lake Merritt Non-native 37.8035 -122.2572
714963 Cohen et al. 2005 (SF Bay Area RAS) 2004 2004-05-24 San Leandro Marina Non-native 37.6966 -122.1932
756168 Introduced Species Study 2005 2005-07-06 Coyote Point Non-native 37.5920 -122.3210
756169 Introduced Species Study 2005 2005-09-07 Dumbarton Bridge Non-native 37.5070 -122.1168
756170 Introduced Species Study 2010 2010-05-31 Dumbarton Bridge Non-native 37.5070 -122.1168
756171 Introduced Species Study 2010 2010-05-31 Redwood Creek - Marina Non-native 37.5021 -122.2130
756172 Introduced Species Study 2010 2010-06-12 China Camp Non-native 38.0025 -122.4617
756173 Introduced Species Study 2010 2010-06-13 Hayward Landing Non-native 37.6447 -122.1543
756174 Introduced Species Study 2010 2010-06-30 Rodeo Marina Non-native 38.0394 -122.2717
760342 Dall 1907 1907 Oyster beds off Alameda Non-native 37.7496 -122.2638
760343 Keep 1911; Hanna 1939; Carlton 1979 1909 San Francisco Bay Non-native 37.8494 -122.3681
760344 Packard 1918a 1912 1912-11-27 U.S. Fish Commission "Albatross" Station D5811 Non-native 37.5890 -122.3157
760345 Packard 1918a 1912 1912-11-27 U.S. Fish Commission "Albatross" Station D5814 Non-native 37.5472 -122.1953
760346 Packard 1918a 1912 Near Key Route Pier, Oakland Non-native 37.8182 -122.3441
760347 Carlton 1979 1920 Bolinas Lagoon Non-native 37.9189 -122.6816
760348 Carlton 1979 1930 Tomales Bay Non-native 38.2100 -122.9400
760349 Carlton 1979 1932 Humboldt Bay Non-native 40.7500 -124.2083
760350 Baily 1932 1932 Lake Merritt Non-native 37.8035 -122.2572
760351 Burch 1945 1939 South San Francisco Bay, off Burlingame Non-native 37.5949 -122.3587
760352 Filice 1954a 1951 San Pablo Bay, offshore of the mouth of Castro Creek Non-native 37.9600 -122.4007
760353 Filice 1954a 1951 Gallinas Creek Marsh Non-native 38.0168 -122.4994
760354 Carpelan 1957 1951 Salt Evaporation Ponds, Alviso Non-native 37.4375 -122.0539
760355 Grodhaus and Keh 1958 1955 1955-06-23 Robert Crown Memorial State Beach (Alameda) Non-native 37.7585 -122.2632
760356 Jones 1961 1955 Point Richmond, Station A Non-native 37.9210 -122.3887
760357 Carlton 1979 1960 San Francisco Bay Non-native 37.8494 -122.3681
760358 Ganssle 1966 1963 San Pablo Bay Non-native 38.0600 -122.3900
760359 Ganssle 1966 1963 Carquinez Strait Non-native 38.0507 -122.1748
760360 Painter 1966b 1963 San Pablo Bay Non-native 38.0600 -122.3900
760361 Vassallo 1969 1969 Mudflats offshore of Hayward Non-native 37.6250 -122.1558
760362 Carlton 1979 1970 San Francisco Bay Non-native 37.8494 -122.3681
760363 Wicksten 1978 1978 Coyote Point Non-native 37.5922 -122.3210
760364 Cohen et al. 2005 (SF Bay Area RAS) 2004 2004-05-28 Rodeo Marina, San Pablo Bay Non-native 38.0391 -122.2711
760365 Brandt et al. 2010 2005 Robert W. Crown Memorial State Beach (Alameda) Non-native 37.7585 -122.2632
760366 Recher 1966 1962 near Mouth of San Francisquito Creek Non-native 37.4658 -122.1156
760367 California Academy of Sciences Invertebrate Zoology Collections Database 1973 1973-08-01 Coyote Point Non-native 37.5922 -122.3210
760368 Thompson and Nichols 1981; Hopkins 1986 1973 1973-02-15 off Charleston Slough (nearshore) Non-native 37.4567 -122.0900
760369 Thompson and Nichols 1981; Hopkins 1986 1973 1973-08-24 off Charleston Slough (nearshore) Non-native 37.4567 -122.0900
760370 Thompson and Nichols 1981; Hopkins 1986 1973 1973-08-24 off Charleston Slough (intermediatel) Non-native 37.4633 -122.0825
760371 Thompson and Nichols 1981; Hopkins 1986 1973 1973-02-15 off Charleston Slough (near main channel) Non-native 37.4708 -122.0733
760372 Thompson and Nichols 1981; Hopkins 1986 1973 1973-08-24 off Charleston Slough (near main channel) Non-native 37.4708 -122.0733
760373 Thompson and Nichols 1981; Hopkins 1986 1973 1973-01-31 off Mowry Slough (in main channel) Non-native 37.4742 -122.0692
760374 Thompson and Nichols 1981; Hopkins 1986 1973 1973-02-15 off Mowry Slough (near main channel) Non-native 37.4783 -122.0650
760375 Thompson and Nichols 1981; Hopkins 1986 1973 1973-08-24 off Mowry Slough (near main channel) Non-native 37.4783 -122.0650
760376 Thompson and Nichols 1981; Hopkins 1986 1973 1973-02-15 off Mowry Slough (intermediate) Non-native 37.4858 -122.0567
760377 Thompson and Nichols 1981; Hopkins 1986 1973 1973-08-24 off Mowry Slough (intermediate) Non-native 37.4858 -122.0567
760378 Thompson and Nichols 1981; Hopkins 1986 1973 1973-08-15 off Mare Island Non-native 38.0633 -122.2650
760379 Thompson and Nichols 1981; Hopkins 1986 1973 1973-02-02 San Pablo Bay (near channel) Non-native 38.0375 -122.3625
760380 Thompson and Nichols 1981; Hopkins 1986 1973 1973-08-15 San Pablo Bay (near channel) Non-native 38.0375 -122.3625
760381 Thompson and Nichols 1981; Hopkins 1986 1973 1973-02-14 off San Leandro Harbor Non-native 37.6917 -122.2050
760382 Thompson and Nichols 1981; Hopkins 1986 1973 1973-01-31 off Foster City (in main channel) Non-native 37.5750 -122.2208
760383 Zucca 1954 1950 Dumbarton Bridge Marsh Non-native 37.5006 -122.1311

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