Invasion History
First Non-native North American Tidal Record: 1938First Non-native West Coast Tidal Record: 1938
First Non-native East/Gulf Coast Tidal Record:
General Invasion History:
Mytilicola orientalis is a parasitic copepod known from oysters (Crassostrea gigas, Pacific Oyster; Ostrea lurida, Olympia Oyster) and mussels (Mytilus crassitesta, M. edulis, M. trossulus, M. californianus) (Grizel 1985; Goater and Weber 1996). It also parasitizes clams (Protothaca staminea, Pacific Littleneck; Venerupis philippinarum, Japanese Littleneck), and the gastropod Crepidula fornicata (Rankin 1943, cited by Carlton 1979; Bower et al. 1992). It was described in 1935 from the Seto Inland Sea, Japan, from the bivalves C. gigas (Pacific Oyster) and M. crassitesta (the Asian Black Mussel) (Mori 1935, cited by Odlaug 1946). It has been introduced to Western North America from Morro Bay, California to British Columbia (Bernard 1969; Quayle 1969; Carlton 1979) and the Northeast Atlantic from France (Grizel 1985) to Ireland (Steele and Mulcahy 2001), the Netherlands (Stock 1993), and the French Mediterranean Coast (Clanzig 1989).
North American Invasion History:
Invasion History on the West Coast:
Mytilicola orientalis was first reported from North American waters in 1938 from Willapa Bay, Washington (WA) in Crassostrea gigas (Wilson 1938; cited by Carlton 1979). By 1943, it was reported from Puget Sound, WA (Rankin 1943, cited by Carlton 1979; Odlaug 1946). Its pattern of spread is difficult to discern and it was probably introduced to many locations with early plantings of Pacific Oysters around 1902, and not recognized until after the species was described. This parasite has been found in cultured oysters in Morro Bay, Elkhorn Slough, Tomales Bay, and Drakes Estero, California; and Yaquina Bay, Oregon (Hedgpeth 1962, cited by Carlton 1979; Chew 1965; Katkansky et al. 1967; Katkansky and Warner 1974, cited by Carlton 1979). In San Francisco and Humboldt Bays, it was found in Olympia Oysters (O. lurida) and mussels (Mytilus spp.) (Chew et al. 1965, Katkansky et al. 1967, Bradley and Siebert 1978, all cited by Carlton 1979). In southern British Columbia waters, M. orientalis is widespread in the Strait of Georgia and in Barkley Sound on the western side of Vancouver Island, in C. gigas, M. trossulus, and V. phillipinarum (Quayle 1969; Carlton 1979; Bower et al. 1992; Goater and Weber 1996).
Invasion History on the East Coast:
Mytilicola orientalis was first collected in European waters in 1977, in the Bay of Arcachon, France, on the Bay of Biscay (Goulletquer et al. 2002). In 1979, it was found in Marennes-Oleron, also on the Bay of Biscay (Goulletquer et al. 2002) and in the Mediterranean, in the Thau Lagoon, Sette, France (Clanzig 1989). All of these areas are extensively used for Pacific Oyster culture.
Description
The larval nauplius and copepodite stages of Mytilicola orientalis are planktonic, but the adults settle inside the intestine of a bivalve, where they metamorphose into greatly modified sedentary wormlike forms, with their appendages greatly reduced (Grizel 1985; Goater and Weber 1996). The adult female is 10 to 12 mm in length, and 1.33 mm wide at the largest section. The head is separate from the thorax. The antennules have four segments; the antennae have two. The antennae are modified into hooks used to cling to the host's tissue. The thorax consists of five segments with triangular lateral extensions. The genital segment is fused with the thoracic segments. The female produces paired egg sacs about 7 mm length, containing approximately 200 eggs. The abdomen is narrower than the genital segment and ends in two triangular outgrowths (Grizel 1985; Fisheries and Oceans Canada 2009).
The development of M. orientalis is unknown, but is probably similar to that of M. intestinalis, which consists of 2 nauplius stages, 5 copepodite stages, and a pre-adult stage, before metamorphosis into the parasitic adult (Gee and Davey 1986).
Taxonomy
Taxonomic Tree
Kingdom: | Animalia | |
Phylum: | Arthropoda | |
Subphylum: | Crustacea | |
Class: | Maxillopoda | |
Subclass: | Copepoda | |
Order: | Cyclopoida | |
Family: | Mytilicolidae | |
Genus: | Mytilicola | |
Species: | orientalis |
Synonyms
Potentially Misidentified Species
Mytilicola intestinalis is aprasite primarily of Mytilus sp., native to the Mediterranean and introduced to the North Sea. There are morphological differences, but genetic methods are recommended for identification At least one study has mis-identified M. orientalis as M. intestinalis (Goedknecht et al. 2018).
Mytilicola porrectus
Parasite of Geukensia demissa and Mercenaria mercenaria, described from Louisiana
Ecology
General:
Mytilicola orientalis is a parasitic copepod, capable of infecting a wide range of bivalve molluscs. Its most common host is the Pacific Oyster (Crassostrea gigas), but it is known from Ostrea lurida (Olympic Oyster), O. edulis (European Oyster), Mytilus coruscus (Japanese Black Mussel), M. edulis (Blue Mussel), M. galloprovincialis (Mediterranean Mussel), M. trossulus (Bay Mussel), M. californianus (California Mussel), Protothaca staminea (Pacific Littleneck), Venerupis philippinarum (Japanese Littleneck), and the gastrood Crepidula fornicata (Common Atlantic Slippersnail) (Rankin 1943, cited by Carlton 1979; Grizel 1985; Bower et al. 1992; Goater and Weber 1996). The wormlike adult female and male mate inside the host's intestine. The female produces paired egg sacs which hatch into naupli.
The life cycle of M. orientalis has not been studied, but in the similar M. intestinalis, there are two nauplius stages, and 5 copepodite stages, all non-feeding. The planktonic stages are filtered out by the bivalve, and remain within, developing into parasitic adults (Gee and Davies 1986). Patterns of infection suggest that dispersal distance in mussel beds is usually short, because the intense filtration of the bivalves remove the larvae from the water column. The number of copepods per mussel increases with mussel size, but decreases with tidal height, probably because of less time for infection (Goater and Weber 1996).
Food:
Crassostrea gigas; other bivalves
Trophic Status:
Parasite
ParasHabitats
General Habitat | Oyster Reef | None |
General Habitat | Marinas & Docks | None |
General Habitat | Rocky | None |
Salinity Range | Polyhaline | 18-30 PSU |
Salinity Range | Euhaline | 30-40 PSU |
Tidal Range | Subtidal | None |
Tidal Range | Low Intertidal | None |
Tidal Range | Mid Intertidal | None |
Vertical Habitat | Epibenthic | None |
Tolerances and Life History Parameters
Minimum Reproductive Salinity | 9.6 | ~50% hatching (Brenner et al. 2019) |
Maximum Length (mm) | 12 | Female (Grizel 1985) |
Broad Temperature Range | None | Cold temperate-Warm temperate |
Broad Salinity Range | None | Mesohaline-Euhaline |
General Impacts
The parasitic copepod Mytilicola orientalis infects oysters, mussels, and clams, including such commercially important species as the Pacific Oyster (Crassostrea gigas), Olympic Oyster (Ostrea lurida), European Oyster (O. edulis), Blue Mussel (Mytilus edulis). Impacts of parasitism on oysters appear to be mostly nonlethal, including local damage to intestinal tissue, and decreased condition factors (increased water, decreased fat content) (Odlaug 1946; Bernard 1969; Grizel 1985; Steele and Mulcahy 2001; Fisheries and Oceans Canada 2009). The extent of damage to mussels is unclear, but heavy infections can lead to mortality (Fisheries and Oceans Canada 2009). This parasite was included on a list of the '100 Worst Invaders' in the Mediterranean Sea (Streftaris and Zenetos 2006).Economic Impacts
Fisheries: Parasitism by Mytilicola orientalis rarely kills oysters, but can lower their condition factor (increased water and decreased fat content), affecting the perceived quality of the oysters (Odlaug 1946; Grizel 1985; Fisheries and Oceans Canada 2009).
Ecological Impacts
Parasitism: Infection by Mytilicola orientalis appears to rarely result in mortality of oysters, but tissue damage to intestinal tissue and scar formation can reduce the efficiency of digestion, and contributes to decreased condtion factor (increased water content, decreased fat) (Odlaug 1946; Katkansky et al. 1967; Grizel 1985; Fisheries and Oceans Canada 2009). These impacts were variable with geography and season (Deslou-Paoli 1981, cited by Fisheries and Oceans Canada 2009). In Ireland, infection by M. orientalis did not directly affect health or quality of Crassostrea gigas, but was associated with increased infestations by shell-boring Polydora spp. (Steele and Mulcahy 2001).
Regional Impacts
NEP-IV | Puget Sound to Northern California | Ecological Impact | Parasitism | ||
Infection with M. orientalis resulted in reduced condition factor in Olympia Oyster (Ostrea lurida) in Willapa Bay (Oldaug 1946). Reduced condition factor was also reported in infected Pacific Oysters (Crassostrea gigas) in Humboldt, Yaquina, and Willapa Bays. However, no relation was seen between infection and mortality (Chew et al. 1965; Katkansky et al. 1967). | |||||
NEP-IV | Puget Sound to Northern California | Economic Impact | Fisheries | ||
Infection resulted in reduced condition factor (increased water, reduced fat) in Olympia Oyster (Ostrea lurida) in Willapa Bay (Oldaug 1946). Reduced condition factor was also reported in infected Pacific Oysters (Crassostrea gigas) in Humboldt, Yaquina, and Willapa Bays. However, no relation was seen between infection and mortality (Chew et al. 1965; Katkansky et al. 1967). | |||||
P130 | Humboldt Bay | Ecological Impact | Parasitism | ||
Reduced condition factor was also reported in infected Pacific Oysters (Crassostrea gigas) in Humboldt, Yaquina, and Willapa Bays. However, no relation was seen between infection and mortality (Chew et al. 1965; Katkansky et al. 1967). | |||||
P130 | Humboldt Bay | Economic Impact | Fisheries | ||
Reduced condition factor was also reported in infected Pacific Oysters (Crassostrea gigas) in Humboldt, Yaquina, and Willapa Bays. However, no relation was seen between infection and mortality (Chew et al. 1965; Katkansky et al. 1967). Reduced condition factor (smaller body mass, higher water content, less fat) reduces the quality of oysters. | |||||
NEP-V | Northern California to Mid Channel Islands | Economic Impact | Fisheries | ||
Reduced condition factor of oysters |
|||||
CA | California | Ecological Impact | Parasitism | ||
Reduced condition factor was also reported in infected Pacific Oysters (Magallana gigas) in Humboldt, Yaquina, and Willapa Bays. However, no relation was seen between infection and mortality (Chew et al. 1965; Katkansky et al. 1967). |
|||||
CA | California | Economic Impact | Fisheries | ||
Reduced condition factor of oysters Reduced condition factor was also reported in infected Pacific Oysters (Magallana gigas) in Humboldt, Yaquina, and Willapa Bays. However, no relation was seen between infection and mortality (Chew et al. 1965; Katkansky et al. 1967). Reduced condition factor (smaller body mass, higher water content, less fat) reduces the quality of oysters. |
Regional Distribution Map
Bioregion | Region Name | Year | Invasion Status | Population Status |
---|---|---|---|---|
P080 | Monterey Bay | 1974 | Non-native | Established |
P090 | San Francisco Bay | 1974 | Non-native | Established |
P070 | Morro Bay | 1974 | Non-native | Established |
P100 | Drakes Estero | 1967 | Non-native | Established |
P130 | Humboldt Bay | 1963 | Non-native | Established |
P110 | Tomales Bay | 1962 | Non-native | Established |
NEP-V | Northern California to Mid Channel Islands | 1962 | Non-native | Established |
NEP-IV | Puget Sound to Northern California | 1938 | Non-native | Established |
Occurrence Map
OCC_ID | Author | Year | Date | Locality | Status | Latitude | Longitude |
---|---|---|---|---|---|---|---|
697030 | Chew et al 1964a | 1963 | 1963-02-19 | State Native Oyster Reserve No. 1, Arcata Bay | Non-native | 40.8148 | -124.1279 |
697114 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Eel River Wildlife Area | Non-native | 40.7566 | -124.1946 | |
697451 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Mad River Slough - Samoa Blvd. Bridge | Non-native | 40.8652 | -124.1505 | |
697497 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Klopp Lake | Non-native | 40.8553 | -124.0919 | |
697658 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Del Norte Street | Non-native | 40.7907 | -124.1879 | |
697945 | Bradley and Siebert 1978 | 1974 | Berkeley Marina, San Francisco Bay | Non-native | 37.8664 | -122.3150 | |
698262 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Hookton Slough | Non-native | 40.6775 | -124.2218 | |
698654 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Samoa Bridge, West | Non-native | 40.8218 | -124.1702 | |
698655 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Samoa Bridge, Middle | Non-native | 40.8138 | -124.1593 | |
699672 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Eureka Slough, Lower | Non-native | 40.8068 | -124.1437 | |
700061 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Southport Landing | Non-native | 40.6952 | -124.2494 | |
700237 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | South Eureka Marina | Non-native | 40.8017 | -124.1807 | |
700660 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Hilfiker Road | Non-native | 40.7720 | -124.1960 | |
700675 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Jacoby Creek | Non-native | 40.8435 | -124.0838 | |
701074 | Bradley and Siebert 1978 | 1930 | San Francisco Bay | Non-native | 37.8494 | -122.3681 | |
701949 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Fields Landing | Non-native | 40.7258 | -124.2213 | |
702833 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Coast Guard Cove | Non-native | 40.7631 | -124.2200 | |
702898 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Bracut | Non-native | 40.8313 | -124.0845 | |
703023 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Samoa Bridge, East | Non-native | 40.8091 | -124.1546 | |
703095 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Samoa Boat Ramp | Non-native | 40.7722 | -124.2124 | |
703156 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | Mad River Slough - Lanphere Christensen Dunes Bridge | Non-native | 40.8979 | -124.1356 | |
703603 | Boyd et al. 2002 (Humboldt Bay Report) | 2002 | North Bay Oyster Beds | Non-native | 40.8230 | -124.1257 | |
757984 | National Museum of Natural History Collections Database | 1961 | 1961-08-28 | Drakes Estero | Non-native | 38.0474 | -122.9422 |
757985 | National Museum of Natural History Collections Database | 1961 | 1961-08-28 | Humboldt Bay near Eureka | Non-native | 40.8225 | -124.1464 |
757986 | National Museum of Natural History Collections Database | 1961 | 1961-09-20 | Drakes Estero | Non-native | 38.0474 | -122.9422 |
757987 | National Museum of Natural History Collections Database | 1961 | 1961-10-02 | Drakes Bay | Non-native | 38.0186 | -122.9319 |
757988 | Katkansky and Warner 1968 | 1966 | Humboldt Bay | Non-native | 40.7498 | -124.2095 | |
757989 | Katkansky and Warner 1968 | 1967 | Humboldt Bay | Non-native | 40.7498 | -124.2095 | |
757990 | Katkansky and Warner 1968 | 1968 | Humboldt Bay | Non-native | 40.7498 | -124.2095 | |
757991 | Johnson and Chew 1969 | 1969 | Humboldt Bay | Non-native | 40.7498 | -124.2095 | |
757992 | Katkansky and Warner 1974, cited in Carlton 1979 | 1974 | Tomales Bay | Non-native | 38.2100 | -122.9400 | |
757993 | Katkansky and Warner 1974, cited in Carlton 1979 | 1974 | Drakes Estero | Non-native | 38.0474 | -122.9422 | |
757994 | Katkansky and Warner 1974, cited in Carlton 1979 | 1974 | Elkhorn Slough | Non-native | 36.8086 | -121.7856 | |
757995 | Katkansky and Warner 1974, cited in Carlton 1979 | 1974 | Morro Bay | Non-native | 35.3378 | -120.8513 |
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