The introduction to Japan of the Titan barnacle, Megabalanus coccopoma (Darwin, 1854) (Cirripedia: Balanomorpha)

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The introduction to Japan of the Titan barnacle, Megabalanus coccopoma (Darwin, 1854) (Cirripedia: Balanomorpha) Toshi Yamaguchi*, Y. Ohshiro, A. Fujimoto, M. Kiuchi, M. Otani, I. Ueda, and H. Kawai *present address: Kanagawa University

Biofouling, Vol. 25, No. 4, May 2009, 325 333. The introduction to Japan of the Titan barnacle, Megabalanus coccopoma (Darwin, 1854) (Cirripedia: Balanomorpha) and the role of shipping in its translocation T Yamaguchi 1, Prabowo RE 1,2, Ohshiro Y 3, Shimono T 4, Jones D 5, Kawai H 4, Otani M 6, Oshino A 7, Inagawa S 1, Akaya T 3, and Tamura I 3 Biofouling The Journal of Bioadhesion and Biofilm Research The type materials of Megabalanus coccopoma from Panama wasn t used in this paper.

Megabalanus coccopoma Buoys for seaweed culture were established at entrance of Tokyo Bay for 6 months from Sep 2008 to Feb 2009. Megabalanus coccopoma reaches to maturity within 6 months.

On Megabalanus coccopoma (Darwin 1854) Taxonomy: Darwin (1854): Described new variety Balanus tintinnabulum var. (7) coccopoma Darwin in 11 varieties of B. tintinnabulum. Pilsbry (1917): Described new subgenus and subspecies Balanus (Megabalanus) tintinnabulum coccopoma Darwin in 7 subspecies of subgenus Megabalanus. Yamaguchi (1973): Described species level taxonomy 0n Japanese megabalanids B. (M.) rosa and B. (M.) volcano based on their reproductive isolation. Newman (1979): Described new genus Megabalanus separated from genus Balanus. Geographic Distribution: Historically known at the East Pacific from Baja California to Ecuador Known History of Invasion: 1980s: South Brazil 1987: San Diego, California, USA (Newman & McConnaughey 1987), Belgium (Kerckhof & Cattrijsse 2001) 2002~2006s: Louisiana, N. Florida, Georgia, N. Carolina, East USA

Iron Carrier Ship A MIZUSHIMA Port, OKAYAMA, JAPAN, Sep. 21, 2007 Sep. 21, 2007 at Mizushima Port Amphibalanus amphitrite Amphibalanus eburneus Amphibalanus improvisus Amphibalanus reticulatus (Japan+ Japan+) Austrobalanus imperator (Australian) Balanus trigonus Chirona amaryllis Chthamalus challengeri (Japan+ Japan+) Fistulobalanus albicostatus (Japan+ Japan+) Lepas anserifera Megabalanus coccopoma Megabalanus rosa (Japan+ Japan+) Megabalanus volcano (Japan+ Japan+) Tesseropora sp. Tetraclita japonica (Japan+ Japan+) Yamaguchiella coerulescens underline: world wide Jan. 5, 2009 at Chiba Port Megabalanus coccopoma Megabalanus rosa (Japan+ Japan+) Megabalanus volcano (Japan+ Japan+) Megabalanus occator (Japan+ Japan+)

Ship A

color & surface M. coccopoma M. rosa M. volcano growth ridge 1. Megabalanus coccopoma growth ridge 2. M. rosa spur spur Megabalanus coccopoma was described from the Pacific coast of Panama and is well known as the allied species in the Atlantic Ocean. Yamaguchi et al. (2009) is the first report from the western Pacific. Megabalanus rosa is the endemic species known from Japan since the Miocene. Megabalanus volcano is also the endemic species known from Japan, Taiwan, Hong Kong. The Holocene fossil was found in Japan. Shell walls: color and nature of surface are different. Growth ridges of scutum and spur of tergum are different. growth ridge 3. M. volcano spur After Yamaguchi et al. (2009)

Information of DNA amplification and sequencing Polymerase chain reaction (PCR) amplifications of mitochondrial cytochrome c oxidize COI were amplified partially (383 bp) using ABI 2720 Thermal cycler. A forward-reverse primer pair and thermocycling protocol, BF2 5 -TGTAATTGTTACTGCTCATGC-3 and BR2 5 -ACCAAARAAYCAGAATAAGTGTTG-3 based on Sotka et al. (2004), was performed at 94 o C for 60 s, 40 cycles at 92 o C for 40 s, 52 o C for 60 s, 72 o C for 90 s and a final extension of 72 o C for 7 min.

Three phylogenetic trees M. volcano M. volcano M. volcano M. rosa M. rosa M. rosa M. coccopoma M. coccopoma M. coccopoma Bayesian Inference (BI) Neighbor Joining (NJ) Maximum Parsimony (MP) mtdna COI gene 426 bp Yamaguchi et al. 2009 Outgroup: Tetraclita japonica Pilsbry

Five Populations (Japan, Panama, Brazil Brazil, Australia,, & Ship hull A ) NJ Tree mtdna COI BF2- BR2 383bp ML Tree Japan Panama Brazil Australia Ship hull A No genetic distinction between any Ooshiro (2008MS), Fujimoto (2010MS), Kiuchi (2010MS) population

Haplotype networks among five populations of Japan, Panama, Brazil, Australia,, & Ship-A Maximum difference is only 13 bp (3.3%). Japan Panama Brazil Australia Ship hull Total number of individuals: 70 A single haplotype network! No haplotype restriction in any Ooshiro (2008MS), Fujimoto (2010MS), Kiuchi (2010MS) Genetic variability is quite low. local population, that is same population or same gene pool. No reproductive isolation among five remote populations. mtdna COI BF2-BR2 383bp 2

Life history: planktic and sessile stages Nauplius Cypris Larvae: Larvae: Planktic Planktic Migration in sessile stage is depend on moving of ships or floating materials as substrata of barnacles. Natural dispersal dispersal Adult Juvenile Life history of barnacle Metamorphose to juvenile Cypris attached on substratum Juveniles Juveniles to Adults: Adults: Sessile Sessile No migration migration by themselves, themselves, but transfer with movement movement of substratum, substratum, such as ship hull Image of life history is from HP of Professor K. Okano, Akita University.

Panama Canal 2008.09 Panama Megabalanus Isla Taboga, coccopoma Panama Caribbean Isla Taboga, Panama Pacific Isla Taboga, Panama

Pink symbol: Light buoy Blue symbol: Rocky shore Distribution in Japan Last update: May 22, 2010 Northern limit First finding port Mizushima in 2007 Ship hull, Tanker Oldest discovery record in Japan 1978.08.11 Muroto, Set Fish Net Oldest settlement record in Japan 1981.07.27 Found at 155 localities in Japan Southern limit

Pacific Ocean Pink symbol: Light buoy Blue symbol: Rocky shore Tokyo Bay Tokyo Tokyo Bay Bay Sagami Bay Sagami Bay Sagami Bay Pacific Pacific Ocean Ocean

On buoys for farming Wakame seaweed, Sep 2008 to Feb 2009 M. rosa M. coccopoma

Life history and Ecology Reported by: J. Masterson, Smithsonian Marine Station, Page last updated: December 1, 2007 Temperature: Cold temperate to tropical Salinity: High saline to brackish (Kerckhof 2002) Growth: Rapid growth (Tibbetts 2007) Our understanding: General characteristics above menti0ned are identical with those of other invasion species. No report on Reproduction and larvae development. However, we can see juveniles on light buoys of Tokyo Bay in a whole year, unlike M. rosa in winter and M. volcano in summer in Japan. Megabalanus coccopoma is naturalized in Japan.

Balanus amphitrite complex including genera Amphibalanus & Fistulobalanus More than 6 species are found on a floating bamboo. High diversity on Balanus amphitrite complex is found in Indo-West Pacific.

Indo-West Pacific Balanidae 地球環境研究総合推進費研究計画説明 Amphibalanus amphitrite is an introduced species well known in whole world. The other are the endemic at SE Asia of Indo-West Pacific.

Native Fistulobalanus albicostatus Genetic comparison among 2 populations using COI gene 405 bp Tokyo Taiwan Tokyo Differentiation in area Taiwan There are four differences (sites) of substitution between two local populations of Tokyo and Taiwan. Tokyo Taiwan 2140 2218 2257 2438 adenine thymine cytosine guanine The four substitutions separated two local groups. Unpublished data by my student S. Inagawa

Native Fistulobalanus kondakovi Genetic comparison among 3 populations using COI gene 433 bp Tokyo Australia Differentiation in area Philippine Tokyo There are nine differences (sites) of substitution between three local populations of Tokyo, Philippine, and Australia. 2085 2118 2183 2281 2319 2376 2463 2487 2490 adenine thymine Philippine cytosine guanine Australia Unpublished data by my student S. Inagawa

Native Amphibalanus reticulatus Genetic comparison among 4 populations using COI gene 407 bp Philippine Samoa Philippine Differentiation in area Samoa Thailand Tokyo Philippine Samoa Thailand 2140 2245 2395 2465 adenine thymine cytosine guanine Tokyo Four local populations are separated to three groups of Tokyo, Thailand, and group of Philippine and Samoa by four substitution. Unpublished data by my student S. Inagawa

Introduced species Amphibalanus amphitrite Genetic comparison among 6 populations using COI gene 384 bp No differentiation in area There is no differentiation among six local populations. Amami Island, Japan Tokyo, Japan Java Island, Indonesia New Caledonia Philippine Samoa Unpublished data by my student S. Inagawa

Conclusion In spite of the vast geographical distances between five populations of Panama, Brazil, Australia, Japan and Ship hull, the haplotype analysis of M. coccopoma suggests that there is single haplotype network. There is no haplotype restriction in any local population. All populations of M. coccopoma examined seem to be same population or same gene pool. The genetic characteristics of M. coccopoma seems to be keeping by the multiple-introduction and transportation of a large number of barnacles by ships. M. coccopoma has bee naturalized in Japan now.