Invasion History
First Non-native North American Tidal Record: 1871First Non-native West Coast Tidal Record: 1871
First Non-native East/Gulf Coast Tidal Record:
General Invasion History:
Limnoria tripunctata is a cosmopolitan wood-boring isopod, found through most of the warmer waters of the world. This species was lumped with L. lignorum, a cold-water, high-latitude species, until they were separated by Menzies (1957). The native region of L. tripunctata is not clear—it may have an Indo-Pacific origin (Kensley, personal communication; Schotte, personal communication), and is widely distributed there, from South Africa to Japan, Polynesia, and Australia (Wallour 1960; Cookson 1990). It is also widespread on both sides of the Atlantic, from Cape Cod to Argentina, and from Portugal to Ghana (Kensley and Schotte 1987). The history of this species in the Atlantic is uncertain, since it was only recognized in 1952. However, Menzies (1957) identifies records and descriptions of ‘L. lignorum’ from the Southeastern US, as early as 1899, as L. tripunctata. Limnoria tripunctata may have been present in the Atlantic for centuries before its description. We regard it as cryptogenic on both sides of the Atlantic, except around the British Isles, where it seems to be a recent arrival, often associated with thermal effluents (Jones 1963).
In the Pacific, Limnoria tripunctata was first reported in Los Angeles Harbor, California (CA) in 1871 (Carlton 1979), and San Diego Bay in 1876 (USNM 2286, collected by R. Hemphill, re-identified as L. tripunctata by Menzies, U.S. National Museum of Natural History 2007). By 1960, it was known from Balboa, Peru (Wallour 1960); the Gulf of California and Bahia San Quintin, Mexico (Menzies 1957); and San Diego Bay, Mission Bay, La Jolla, Santa Catalina Island, Newport Bay, Los Angeles-Long Beach Harbors, and Port Hueneme, California (Menzies 1957; Wallour 1960; Carlton 1979).
North American Invasion History:
Invasion History on the West Coast:
Limnoria tripunctata appears to be definitely introduced on the West Coast of North America, where it was first reported in Los Angeles Harbor, California (CA) in 1871 (Carlton 1979), and San Diego Bay in 1876 (USNM 2286, collected by R. Hemphill, re-identified as L. tripunctata by Menzies, U.S. National Museum of Natural History 2007). It now ranges from the Panama Canal to Vancouver Island, though it appears to be patchily distributed, in particular estuaries, but not others (Menzies 1952; Wallour 1960; Carlton 1979; Quayle 1992). By 1960, it was known from Balboa, Peru (Wallour 1960); the Gulf of California and Bahia San Quintin, Mexico (Menzies 1957); and San Diego Bay, Mission Bay, La Jolla, Santa Catalina Island, Newport Bay, Los Angeles-Long Beach Harbors, and Port Hueneme, California (Menzies 1957; Wallour 1960; Carlton 1979).
In the latter decades of the 20th century, Limnoria tripunctata appears to have extended its range north. It was not found north of San Francisco in 1950s surveys, which included sampling in Coos Bay, Oregon (OR) and Puget Sound, Washington (WA) (Menzies 1957; Wallour 1960). However, it was reported in Coos Bay in 1983 (Carlton 1989); Yaquina Bay, Willapa Bay and the Straits of Georgia in 1964 (Quayle 1992); and Puget Sound in 1998 (Cohen et al. 1998). Limnoria tripunctata in British Columbia is found mainly in oyster-growing areas and semi-enclosed coves, with limited wave action and warmer summer temperatures, but at least five occurrences are known from locations with no history of oyster culture. Wooden boxes used to transport oysters are a likely vector for local distribution of woodborers in British Columbia waters (Quayle 1992).
Invasion History in Hawaii:
Limnoria tripunctata is considered introduced in Hawaii, where it was first found in 1922 in Pearl and Honolulu Harbors on Oahu, and Nauwili Harbor, Kauai (originally identified as L. lignorum; Carlton and Eldredge 2009). It has also been found on Midway Island (Wallour 1960).
Invasion History Elsewhere in the World:
The native region of Limnoria tripunctata is unknown, because of its late description and distinction from L. lignorum. Limnoria tripunctata is now widespread on the East Coast of North America from Boston Harbor to the Panama Canal, and in South America from Uruguay and Argentina. It is widespread in Europe from La Rochelle, France to Portugal and the Azores, and through the Mediterranean (Bourdillon 1958; Jones 1972, Sen et al. 2010; Borges et al. 2014c; Borges and Costa 2014). In British waters, L. tripunctata appears to be a recent colonist, becoming established in thermal effluents, and colonizing adjacent waters (Jones 1963; Eltringham and Hockley, 1963; Coughlan 1977). In England, it was first found in 1958 in Southampton Water, on the English Channel, and was subsequently found in the Welsh ports of Burry and Swansea on the Irish Sea (Jones 1963). It was reported from Ghana, in the Gulf of Guinea (Cookson 1990), where we consider it cryptogenic. In Cape Town, South Africa, it was first reported from the docks of Table Bay in 2008 (Mead et al. 2011b).
Limnoria tripunctata is widespread in the Indian Ocean and the western Pacific, from China and Japan to Australia and Fiji (Wallour 1960; Nair 1984; Cookson 1990; Huang 2001; US National Museum of Natural History 2015). This gribble is considered nonindigenous in New Zealand, and was first reported in 1964 (McGuire 1964, cited by Cookson 1990; Cranfield et al. 1998).
Description
Limnoria tripunctata is a gribble, a small, marine, wood-boring isopod. Limnoria tripunctata has a small, nearly cylindrical body. The cephalon (head region) is compressed and ovoid, with lateral eyes. The cephalon is distinct from the pereion (thoracic region) and freely rotates. Antennas 1 and 2 are equally anterior, with an obvious scale on Antenna 1. The flagellum of second antenna has 4 segments.The left mandible incisor lacks teeth, instead forming a projecting rasp-and-file device. Uropods are greatly reduced, with the exopod much shorter than the endopod, and bearing an apical claw.
The anterior dorsal surface of the pleotelson bears three symmetrically arranged tubercles anteriorly. The lateral and posterior edges are lined with tubercules. Adults are up to 3.4 mm long, white to pink when alive, and yellow when preserved in alcohol. Description based on information from: Menzies 1957; Cookson 1990; Brusca et al. 2007; and Castelló 2011.
Taxonomy
Taxonomic Tree
Kingdom: | Animalia | |
Phylum: | Arthropoda | |
Subphylum: | Crustacea | |
Class: | Malacostraca | |
Subclass: | Eumalacostraca | |
Superorder: | Peracarida | |
Order: | Isopoda | |
Suborder: | Flabellifera | |
Family: | Limnoriidae | |
Genus: | Limnoria | |
Species: | tripunctata |
Synonyms
Limnoria terebrans (Leach, 1841)
Limnoria tuberculata (Sowinsky, 1884)
Potentially Misidentified Species
Limnoria lignorum has a circumboreal distribution in the northern Atlantic and Pacific, and is presumed to be native throughout this range (Menzies 1957).
Limnoria pfeiferri
None
Limnoria quadripunctata
Limnoria quadripunctata is probably native to the South Pacific, and has been introduced to Europe, the Azores, Bermuda, the West Coast, and South Africa (Menzies 1957; Wallour 1960; Jones 1963; Mead et al. 2011b).
Limnoria tuberculata
Limnoria tuberculata has been variously synonymized with or treated as a separate species from L. tripunctata. It was described from the Black Sea by Sowinsky in 1884. Menzies (1972) identified an apparently reproductively isolated population from Chatham, Massachusetts, as this species. Kensley and Schotte (Kensley and Schotte 1987; Kensley and Schotte 1989) have treated this name as the senior synonym of L. tripunctata, but used 'L. tripunctata' in Kensley et al. (1995). However, Cookson (1990) and Castelló (2011), treat L. tuberculata as a separate species. If it is a distinct species, its records are few and scattered, and little is known of its biology.
Ecology
General:
Limnoria tripunctata has separate sexes, and copulation is internal. Typically, in Limnoria spp., a single pair occupies a boring tunnel, with the female closer to the opening. Brood sizes of L. tripunctata range from 5 to 15 eggs per female. The young are brooded by the female (Becker 1971). Adults and juveniles swarm seasonally, and colonize new pieces of wood. They prefer rough surfaces of relatively soft wood, preferably infected by fungi (Becker 1971).
Limnoria tripunctata inhabits warm-temperate to tropical climates and marine salinities. It tolerates winter temperatures as low as 2 °C (Menzies 1957) and experimental temperatures as high as 30 °C (Beckman and Menzies 1960). Reproduction occurs at 15-30 °C, but development was optimum at 25 °C (Beckman and Menzies 1960). In experiments, this gribble had good survival at salinities of 36-50 PSU, but poor survival (15-50%) at 18 and 24 PSU (Eltringham 1961; Lum 1981). In Southampton Water, England, migration began in June at about 18 °C (Eltringham and Hockley 1963). Limnoria tripunctata digests non-cellulosic carbohydrates in wood, together with some cellulose, and excretes lignin in pellets—all without the aid of gut microflora (Becker 1971; Sleeter et al. 1978). Limnoria spp. host a variety of protozoan epibionts and crustacean symbionts. At least one epibiont, the ciliate Mirofolliculina limnoriae slows the feeding, swimming and growth of Limnoria tripunctata, and so can be regarded as an ectoparasite (Delgery et al. 2006).
Food:
Wood and associated microbiota
Trophic Status:
Herbivore
HerbHabitats
General Habitat | Coarse Woody Debris | None |
General Habitat | Marinas & Docks | None |
General Habitat | Grass Bed | None |
General Habitat | Mangroves | None |
General Habitat | Vessel Hull | None |
Salinity Range | Polyhaline | 18-30 PSU |
Tidal Range | Subtidal | None |
Vertical Habitat | Epibenthic | None |
Life History
Tolerances and Life History Parameters
Minimum Temperature (ºC) | 2 | Field data (Menzies 1957) |
Maximum Temperature (ºC) | 30 | (Beckman and Menzies 1960) |
Minimum Salinity (‰) | 19 | Experimental data (Lum 1981). |
Maximum Salinity (‰) | 50 | Experimental data (Lum 1981). |
Minimum Reproductive Temperature | 15 | Experimental data (Beckman and Menzies 1960) |
Maximum Reproductive Temperature | 30 | Highest tested (Beckman and Menzies 1960) |
Minimum Length (mm) | 2 | Minimum adult size (Menzies 1957; Cookson 1990) |
Maximum Length (mm) | 4 | Minimum adult size (Menzies 1957; Cookson 1990) |
Broad Temperature Range | None | Cold temperate-Tropical |
Broad Salinity Range | None | Polyhaline-Euhaline |
General Impacts
Limnoria tripunctata, a gribble (wood-boring isopod) is a major wood-borer, damaging wooden pilings and ship hulls in warm-temperate to tropical marine waters around the world. It is rare or absent in ports where salinity drops much below 20 PSU (Becker 1971; Lum 1971). Damage to pilings by L. tripunctata has been reported from Boca Grande, Florida (Atwood 1922), Los Angeles (Quayle 1992), San Francisco Bay (Carlton 1979; Cohen and Carlton 1995), British Columbia (Quayle 1992), and England (Jones 1963). Replacement and treatment of pilings, and the effects of toxic compounds, such as creosote and other wood treatments, add to the impacts of Limnoria (Becker 1971).
Regional Impacts
P090 | San Francisco Bay | Economic Impact | Shipping/Boating | ||
Damage to pilings in Oakland estuary, San Francisco Bay, probably due to this isopod, was first noted in 1873 (Merritt 1875, cited by Carlton 1979). | |||||
NEP-V | Northern California to Mid Channel Islands | Economic Impact | Shipping/Boating | ||
Damage to pilings in Oakland estuary, San Francisco Bay, probably due to this isopod, was first noted in 1873 (Merritt 1875, cited by Carlton 1979). | |||||
P050 | San Pedro Bay | Economic Impact | Shipping/Boating | ||
'In Los Angeles, California, this species can reduce the life of a creosote treated piling to about 6 years instead of a possible 40 years in northern waters (Beckman et al. 1957).' (Quayle 1992). | |||||
NEP-VI | Pt. Conception to Southern Baja California | Economic Impact | Shipping/Boating | ||
'In Los Angeles, California, this species can reduce the life of a creosote treated piling to about 6 years instead of a possible 40 years in northern waters (Beckman et al. 1957).' | |||||
CA | California | Economic Impact | Shipping/Boating | ||
Damage to pilings in Oakland estuary, San Francisco Bay, probably due to this isopod, was first noted in 1873 (Merritt 1875, cited by Carlton 1979)., 'In Los Angeles, California, this species can reduce the life of a creosote treated piling to about 6 years instead of a possible 40 years in northern waters (Beckman et al. 1957).' (Quayle 1992)., Damage to pilings in Oakland estuary, San Francisco Bay, probably due to this isopod, was first noted in 1873 (Merritt 1875, cited by Carlton 1979). |
Regional Distribution Map
Bioregion | Region Name | Year | Invasion Status | Population Status |
---|---|---|---|---|
P027 | _CDA_P027 (Aliso-San Onofre) | 2011 | Non-native | Unknown |
P060 | Santa Monica Bay | 1969 | Non-native | Established |
NEP-IV | Puget Sound to Northern California | 1964 | Non-native | Established |
P058 | _CDA_P058 (San Pedro Channel Islands) | 1950 | Non-native | Established |
P062 | _CDA_P062 (Calleguas) | 1950 | Non-native | Established |
P022 | _CDA_P022 (San Diego) | 1949 | Non-native | Established |
P030 | Mission Bay | 1948 | Non-native | Established |
P040 | Newport Bay | 1947 | Non-native | Established |
P020 | San Diego Bay | 1876 | Non-native | Established |
NEP-V | Northern California to Mid Channel Islands | 1875 | Non-native | Established |
P090 | San Francisco Bay | 1875 | Non-native | Established |
P093 | _CDA_P093 (San Pablo Bay) | 1875 | Non-native | Established |
NEP-VI | Pt. Conception to Southern Baja California | 1871 | Non-native | Established |
P050 | San Pedro Bay | 1871 | Non-native | Established |
Occurrence Map
OCC_ID | Author | Year | Date | Locality | Status | Latitude | Longitude |
---|---|---|---|---|---|---|---|
697537 | Reish 1972 | 1972 | Alamitos Bay | Non-native | 33.7502 | -118.1185 | |
697976 | Introduced Species Study | 2011 | 2011-04-21 | Draw Bridge | Non-native | 33.7645 | -118.2428 |
698480 | Introduced Species Study | 2010 | 2010-06-28 | Santa Fe Channel - Front | Non-native | 37.9101 | -122.3644 |
698599 | Cohen et al. 2005 (SF Bay Area RAS) | 2004 | 2004-05-27 | Coyote Point Marina, San Francisco Bay | Non-native | 37.5907 | -122.3180 |
699046 | Introduced Species Study | 2006 | 2006-07-25 | CIYC Guest Slip | Non-native | 34.1641 | -119.2255 |
699215 | Introduced Species Study | 2010 | 2010-06-03 | Treasure Island | Non-native | 37.8149 | -122.3702 |
699319 | Introduced Species Study | 2010 | 2010-07-15 | San Pablo Bay Pumphouse | Non-native | 38.0446 | -122.4326 |
699345 | Introduced Species Study | 2010 | 2010-07-12 | Saint Francis Yacht Harbor | Non-native | 37.8066 | -122.4463 |
699552 | Introduced Species Study | 2010 | 2010-05-31 | Redwood Creek - Shipping | Non-native | 37.5120 | -122.2109 |
700233 | Introduced Species Study | 2006 | 2006-10-10 | The Tuna Club | Non-native | 33.3461 | -118.3268 |
700315 | Introduced Species Study | 2010 | 2010-06-03 | Berkeley Flats/Berkeley Pier | Non-native | 37.8600 | -122.3256 |
700436 | ISS 2000-2002 Survey Data | 2001 | 2001-08-16 | Long Beach Epifaunal 04 | Non-native | 33.7709 | -118.2113 |
700635 | Mendell 1871, cited in Menzies et al. 1963 | 1871 | Los Angeles/Long Beach Harbor Complex | Non-native | 33.7632 | -118.2526 | |
700693 | Reish 1972 | 1972 | Huntington Harbour | Non-native | 33.7216 | -118.0652 | |
700733 | Menzies 1951, 1957 | 1950 | 1950-02-14 | Newport Bay at Pacific Coast Highway Bridge | Non-native | 33.6168 | -117.9048 |
700735 | Introduced Species Study | 2011 | 2011-04-21 | Backside of Working Container Ship Pier | Non-native | 33.7667 | -118.2774 |
700989 | Menzies 1951; Wetzer et al. 1991 | 1948 | 1948-12-23 | Foot of Fanuel Street, Pacific Beach (Mission Bay) | Non-native | 32.7912 | -117.2441 |
701377 | Cohen et al. 2002 (So Cal Exotics RAS) | 2000 | 2000-08-30 | Impound Marina | Non-native | 33.7639 | -118.2444 |
701819 | Introduced Species Study | 2010 | 2010-06-02 | Ballena Bay | Non-native | 37.7661 | -122.2834 |
701902 | Introduced Species Study | 2011 | 2011-05-05 | Ocean Institute Dock | Non-native | 33.4622 | -117.7063 |
701918 | Reish 1972 | 1972 | Anaheim Bay | Non-native | 33.7333 | -118.0894 | |
701938 | Cohen et al. 2005 (SF Bay Area RAS) | 2004 | 2004-05-24 | Coast Guard Island Marina, San Francisco Bay | Non-native | 37.7812 | -122.2458 |
702499 | Menzies 1951; Carlton 1979a; Cohen and Carlton 1995; National Museum of Natural History, Invertebrat | 1876 | San Diego Bay | Non-native | 32.6717 | -117.1439 | |
702537 | Merritt 1875, cited in Carlton 1979 | 1875 | Oakland Estuary, San Francisco Bay | Non-native | 37.7866 | -122.2654 | |
702964 | Cohen et al. 2005 (SF Bay Area RAS) | 2004 | 2004-05-23 | Sierra Point Marina, San Francisco Bay | Non-native | 37.6732 | -122.3807 |
703233 | Menzies 1957 | 1950 | Port Hueneme | Non-native | 34.1496 | -119.2082 | |
703420 | Menzies 1951, 1957 | 1949 | 1949-08-16 | La Jolla | Non-native | 32.8479 | -117.2776 |
703477 | Introduced Species Study | 2011 | 2011-04-07 | Commercial Fishing Dock | Non-native | 34.1696 | -119.2285 |
703573 | Reish 1972 | 1972 | Marina del Rey General Location | Non-native | 33.9759 | -118.4482 | |
704092 | Menzies 1951, 1957 | 1950 | 1950-07-15 | Santa Catalina Island | Non-native | 33.4491 | -118.4934 |
704291 | Cohen et al. 2005 (SF Bay Area RAS) | 2004 | 2004-05-23 | Brisbane Lagoon, San Francisco Bay | Non-native | 37.6862 | -122.3906 |
704545 | ISS 2000-2002 Survey Data | 2000 | 2000-11-08 | Port Hueneme Epifaunal 03 | Non-native | 34.1516 | -119.2067 |
760531 | Macrae 1923 | 1910 | San Diego Municipal Pier | Non-native | 32.7174 | -117.1767 | |
760532 | Kofoid 1921 | 1921 | Southern Pacific Company Dumbarton Cut-Off Bridge (Station 57) | Non-native | 37.4995 | -122.1282 | |
760533 | Kofoid 1921 | 1921 | Oakland Municipal Wharf | Non-native | 37.7945 | -122.2789 | |
760534 | Kofoid and Miller 1923; 1927 | 1922 | 1922-11-19 | Old Fish Cannery Wharf, Los Angeles Harbor | Non-native | 33.7405 | -118.2748 |
760535 | Kofoid and Miller 1923 | 1922 | Los Angeles Harbor | Non-native | 33.7269 | -118.2623 | |
760536 | Kofoid and Miller 1923 | 1922 | Charles R. McCormick Lumber Company Wharf, San Diego | Non-native | 32.6998 | -117.1534 | |
760537 | Macrae 1923 | 1923 | San Diego Bay | Non-native | 32.6717 | -117.1439 | |
760538 | Kofoid and Miller 1927 | 1927 | Southern Pacific Company Dumbarton Cut-Off Bridge (Station 57) | Non-native | 37.4995 | -122.1282 | |
760539 | Neily and Kirkbride 1927 | 1927 | Long Beach [Harbor] | Non-native | 33.7552 | -118.2157 | |
760540 | Graham and Gay 1945 | 1941 | Fruitvale Avenue Bridge | Non-native | 37.7689 | -122.2296 | |
760541 | Menzies 1951, 1957 | 1947 | 1947-04-17 | Newport Bay at Pacific Coast Highway overpass | Non-native | 33.6168 | -117.9048 |
760542 | Menzies 1958 | 1949 | Point San Pedro (Station 1) | Non-native | 37.9857 | -122.4471 | |
760543 | Menzies 1957, 1958 | 1949 | San Rafael [Creek] (at U.S. Highway 101; Station 2) | Non-native | 37.9701 | -122.5218 | |
760544 | Menzies 1958 | 1949 | San Quentin (Station 3) | Non-native | 37.9432 | -122.5033 | |
760545 | Menzies 1958 | 1949 | Point San Quentin (Station 4) | Non-native | 37.9425 | -122.4776 | |
760546 | Menzies 1957, 1958 | 1949 | Belvedere (Station 5 [as Tiburon in Table 1]) | Non-native | 37.8791 | -122.4736 | |
760547 | Menzies 1957, 1958 | 1949 | South Basin (Station 11) | Non-native | 37.7208 | -122.3787 | |
760548 | Menzies 1958 | 1949 | San Mateo Bridge (Station 12) | Non-native | 37.5738 | -122.2624 | |
760549 | Menzies 1958 | 1949 | W end of Dumbarton Bridge (Station 13) | Non-native | 37.4995 | -122.1282 | |
760550 | Menzies 1958 | 1949 | E end of Dumbarton Bridge (Station 14) | Non-native | 37.5121 | -122.1103 | |
760551 | Menzies 1958 | 1949 | Oakland [Emeryville] (Station 15) | Non-native | 37.8312 | -122.2964 | |
760552 | Menzies 1958 | 1949 | Berkeley Yacht Harbor (Station 16) | Non-native | 37.8666 | -122.3151 | |
760553 | Menzies 1957, 1958 | 1949 | Parr-Richmond Pier (Station 17) | Non-native | 37.3644 | -122.3644 | |
760554 | Menzies 1957, 1958 | 1949 | Richmond Ferry Landing (Station 18) | Non-native | 37.9081 | -122.3927 | |
760555 | Menzies 1958 | 1949 | Oleum (Station 19) | Non-native | 38.0470 | -122.2624 | |
760556 | Menzies 1957, 1958 | 1949 | Rodeo (Station 20) | Non-native | 38.0329 | -122.2771 | |
760557 | Menzies 1951, 1957 | 1950 | 1950-02-14 | Upper Newport Bay | Non-native | 33.6473 | -117.8861 |
760558 | Menzies 1951 | 1950 | Berkeley Yacht Harbor | Non-native | 37.8666 | -122.3151 | |
760559 | Barnard 1955 | 1951 | California Yacht Basin (Outer Los Angeles Harbor) | Non-native | 33.7180 | -118.2791 | |
760560 | Menzies 1957, 1958 | 1951 | Los Angeles Harbor, Slip 1 (Station A) | Non-native | 33.7623 | -118.2661 | |
760561 | Menzies 1957, 1958 | 1951 | Los Angeles Harbor, Slip No. 5 (Station B) | Non-native | 33.7648 | -118.2634 | |
760562 | Menzies 1957, 1958 | 1951 | Los Angeles Harbor, Cerritos Channel, eastern side of Henry Ford Bridge (Station D) | Non-native | 33.7663 | -118.2393 | |
760563 | Menzies 1957, 1958 | 1951 | Pontoon Bridge between Terminal Island and Long Beach (Station E) | Non-native | 33.7646 | -118.2211 | |
760564 | Menzies 1957, 1958 | 1951 | Los Angeles Harbor, U.S. Navy Operations Base (Station F) | Non-native | 33.7522 | -118.2387 | |
760565 | Menzies 1957, 1958 | 1951 | Long Beach Harbor Pilot Jetty (Station G) | Non-native | 33.7473 | -118.2157 | |
760566 | Menzies 1957, 1958 | 1951 | Reeves Field Seaplane Hangar Bay (Station H) | Non-native | 33.7460 | -118.2537 | |
760567 | Menzies 1957, 1958 | 1951 | Fish Harbor Inner Breakwater (Station J) | Non-native | 33.7353 | -118.2662 | |
760568 | Menzies 1957, 1958 | 1951 | 500 feet south of Boy Scouts of America Explorer Base (Station L) | Non-native | 33.7147 | -118.2845 | |
760569 | Menzies 1957, 1958 | 1951 | Los Angeles Harbor, Channel Marker No. 5 (Station M) | Non-native | 33.7165 | -118.2679 | |
760570 | Menzies 1957, 1958 | 1951 | Los Angeles Harbor, Berth 70 Municipal Wharf (Station N) | Non-native | 33.7243 | -118.2724 | |
760571 | Menzies 1957, 1958 | 1951 | Berth 236, under Small Boat Fueling Wharf (Station P) | Non-native | 33.7370 | -118.2746 | |
760572 | Menzies 1957, 1958 | 1951 | Los Angeles Harbor, Berth 147 (Station Q) | Non-native | 33.7577 | -118.2740 | |
760573 | Carpelan 1957 | 1951 | Floodgate at Charleston Slough | Non-native | 37.4557 | -122.1009 | |
760574 | Menzies 1957 | 1957 | Berth 59, Los Angeles Harbor (East Channel) | Non-native | 33.7225 | -118.2740 | |
760575 | Turner et al. 1969 | 1961 | Hermosa Beach Artificial Reef | Non-native | 33.8546 | -118.4105 | |
760576 | Schafer 1966 | 1966 | Los Angeles Harbor | Non-native | 33.7269 | -118.2623 | |
760577 | U.S. National Museum of Natural History, Invertebrate Zoology Collection Database | 1968 | 1968-08-02 | Port Hueneme | Non-native | ||
760578 | Reish et al. 1975 | 1972 | Anaheim Bay, Station 15 | Non-native | 33.7385 | -118.0783 | |
760579 | Carlton and Hodder 1995 | 1987 | 1987-09-22 | Humboldt Bay | Non-native | 40.7864 | -124.1922 |
760580 | Carlton and Hodder 1995 | 1987 | 1987-09-25 | San Francisco Bay | Non-native | 37.8494 | -122.3681 |
760581 | Reish et al. 2015 | 2014 | Los Angeles Harbor, Slip 1, Berth 160 (Station A) | Non-native | 33.7629 | -118.2662 | |
760582 | Reish et al. 2015 | 2014 | Los Angeles Harbor, Basin 5 (Station B) | Non-native | 33.7657 | -118.2602 | |
760583 | Reish et al. 2015 | 2014 | Los Angeles Harbor, Consolidated Slip (Station C) | Non-native | 33.7722 | -118.2491 | |
760584 | Reish et al. 2015 | 2014 | Los Angeles Harbor, Cerritos Channel (Station D) | Non-native | 33.7643 | -118.2471 | |
760585 | Reish et al. 2015 | 2014 | Los Angeles Harbor, Fish Harbor (Station J) | Non-native | 33.7356 | -118.2692 | |
760586 | Reish et al. 2015 | 2014 | Los Angeles Harbor, Entrance to West Channel (Station L) | Non-native | 33.7151 | -118.2763 | |
760587 | Reish et al. 2015 | 2014 | Los Angeles Harbor, Port Pilot Station (Station N) | Non-native | 33.7207 | -118.2709 | |
760588 | Reish et al. 2015 | 2014 | Los Angeles Harbor, Entrance to West Basin (Station Q) | Non-native | 33.7566 | -118.2773 | |
760589 | Shaw 1918 | 1918 | near Pomona College Marine Laboratory, Laguna Beach | Non-native | 33.5422 | -117.7859 | |
760590 | Menzies 1957 | 1950 | McNear's Beach | Non-native | 37.9934 | -122.4532 |
References
Atwood, W. G. (1922) Marine borers, Proceedings of the American Society of Civil Engineers 48(6): 1408-1424Becker, Gunther (1971) On the biology, physiology, and ecology of marine wood-boring crustaceans., In: Gareth Jones, E. B.//Eltringham, S. K.(Eds.) Marine borers, fungi, and fouling organisms of wood.. , Brussels. Pp. 303-326
Beckman, Carolyn; Menzies, Robert (1960) The relationship of reproductive temperature and the geographical range of the marine woodborer Limnoria tripunctata., Biological Bulletin 118: 9-16
Beckmann, Carolyn; Menzies, R. J.; Wakeman, C. M. (1957) The biological aspects of attack on creosoted wood by Limnoria, Corrosion 13(3): 32-34
Borges, L. M. S. (2013) Biodegradation of wood exposed in the marine environment: Evaluation of the hazard posed by marine wood-borers in fifteen European sites, International Biodeterioration & Biodegradation 96: 97-104
Borges, L. M. S.; Valente, A. A.; Palma, P.; Nunes, L. (2010) Changes in the wood boring community in the Tagus Estuary: a case study, Marine Biodiversity Records 3: e41
Borges, Luisa M. S.; Costa, Filipe O. (2014) New records of wood-borers (Bivalvia: Teredinidae) and Isopoda, Limnoriidae) from Sao Miguel, Azores with a discussion of some aspects of their biogeography, Acoreana Supplement 10: 109-116
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