<strong>PICES</strong> XIII GP-1799 PosterStock enhancement policy for Japanese red sea bream, Pagrus major, by release ofjuveniles and fisheries managementToyomitsu Horii 1 and Hiromu Zenitani 212Yokosuka Branch of National Research Institute of Fisheries Science, Fisheries Research Agency, 6-31-1 Nagai, Yokosuka 238-0316, JapanE-mail: thorii@affrc.go.jpNational Research Institute of Fisheries and Environment of Inland Sea, Fisheries Research Agency, 2-17-5 Maruishi, Ohno, Saeki, Hiroshima739-0452, JapanJapanese red sea bream is a major target of commercial and recreational fishing, and millions of juveniles have beenreleased each year for stock enhancement since the early 1980s. Recovery rates and expected catches of releasedjuveniles were estimated to be 5-17% and 20-80 tons per million juveniles, respectively, in the case of the southerncoastal area. In this paper, the effects of juvenile release on the sustainable yield from two local stocks, the southerncoastal area and the Seto inland sea area, were evaluated.Numbers of recruits and brood stock biomass during 1983-1993 were estimated with virtual population analysis(VPA) from data of age composition of landed fish. When the relationships between brood stock biomass andrecruits followed the Ricker model, number of 1-year-old recruits in t year (R t ) wasR t = A * E t-1 * exp( -B * E t-1 ) + S t-1 * KHere, A and B are the parameters of the Ricker model curve, and E t is brood stock biomass. S t and K are numbersof released juveniles and the survival rate of released juveniles until becoming 1-year-olds, respectively. A, B and Kwere estimated by the method of least squares. Using these parameters, the relationships among fishing mortality,number of releases and sustainable yield were calculated.The increments of sustainable yield by stocking were estimated to be 20% and 2% in the two local stocks of thesouthern coastal area and the Seto Inland Sea area, respectively, under the current status of fishing mortality andnumber of released juveniles. Differences in increments were caused by differences in stocking impact and fishingmortality. The adequacy of the enhancement policy on the two local stocks is discussed.<strong>PICES</strong> XIII GP-2077 PosterUsing a generalized additive model to predict Bigeye (Thunnus obesus) CPUE at thePalmyra fishing groundsEvan A. Howell and Donald R. KobayashiPacific Islands Fisheries Science Center, National Marine Fisheries Service, NOAA, 2570 Dole Street, Honolulu, HI, 96822-2396, U.S.A.E-mail: Evan.Howell@noaa.govThe fishing grounds around the Palmyra Atoll can account for up to 20% of bigeye and over 55% of yellowfin tunalanded in the Hawaii Long-line Fishery since 1994. The observed availability of these two species of tuna appearsto fluctuate based on environmental conditions, with catches around Palmyra dominated by yellowfin tuna, except inyears of El Niño events. This variability in catch, when compounded with the travel time and cost for Hawaiianvessels, diminishes the desire to fish these productive waters. Modeling techniques were employed to attempt todecipher which parameters are important in determining the catch composition and to produce a basic prediction ofthe magnitude of bigeye catch. Generalized additive models (GAM) were used within a k-fold cross-validationframework to construct a predictive model of bigeye tuna (Thunnus obesus) catch rate on long-line fishing geararound Palmyra Atoll. This approach was contrasted with commonly used stepwise model construction techniquesto examine the effects of overfitting. Preliminary results revealed that two environmental parameters with date andlocations were sufficient to account for close to 70% of the bigeye CPUE. The main environmental parameterrequired by the model was an ecosystem indicator derived from an empirical orthogonal analysis (EOF) of altimetrydata in the Pacific equatorial region. A parsimonious model using several predictor variables was also constructedand found to be satisfactory for predicting long-line fishing success.200
<strong>PICES</strong> XIII GP-1862 PosterSpatial comparison of ocean distribution and feeding habits of sockeye (Oncorhynchusnerka) and pink salmon (O. gorbuscha) in the western Gulf of Alaska during summer 2003Miwako Kitagawa 1 , Katherine W. Myers 2 and Masahide Kaeriyama 112School of Engineering, Hokkaido Tokai University, 5-1-1-1 Minamisawa, Minami-ku, Sapporo, Hokkaido, 005-8601, JapanE-mail: salmon@dm.htokai.ac.jpSchool of Aquatic and Fishery Science, University of Washington, Box 355020, Seattle, WA, 98195-5020, U.S.A.We investigate spatial differences in distribution and feeding habits of sockeye (Oncorhynchus nerka) and pinksalmon (O. gorbuscha) in the western Gulf of Alaska (145-160ºW, 50-58ºN). Sockeye salmon were distributed in amore to the south (51-53ºN, 155-160ºW) than pink salmon (54-56ºN, 155-160ºW). Sockeye were immature andpink salmon were maturing. They consumed diverse prey, such as fishes, squids, amphipods, decapods, andpteropods. Sockeye salmon fed on larger prey (fishes and squids) consisting of higher energy at low CPUEs of bothspecies. Sockeye and pink salmon did not show a shift from small to large prey with increasing body size. Resultsof cluster analysis on stomach contents showed that sockeye salmon fed dominantly on pteropods in coastal waters,decapods in middle waters, and hyperiid amphipods and squids in offshore waters despite unclear results for pinksalmon. Sockeye and pink salmon had a high degree of overlap in feeding niche (C H >0.6) and the same dominantprey, such as pteropods and decapods, in areas of sympatric distribution. These results suggest that sockeye andpink salmon should be omnivorous and opportunistic feeders, feeding on available and abundant prey according tointra- and inter-specific competitions, food composition and oceanic environment.<strong>PICES</strong> XIII GP-1889 PosterIchthyofauna of seamounts in the North PacificLeonid S. Kodolov and Vladimir B. DarnitskyTINRO-Center (Pacific Research Fisheries Center), Laboratory of Far Eastern Seas resources, 4-Shevchenko Alley, Vladivostok, 690950, RussiaE-mail: kodolov@tinro.ruIn 1967, the Russian trawler Astronom found accumulations of boarfish on the Emperor Seamounts. It generatedmuch interest in such underwater features. Later, it was found out that such underwater features, as well as islandsand island arches, play an important role in creating zones of increased efficiency (Kotenev, 1977; Neumann,Krylov, 1979; Darnitsky, 1980; Uchida, Hayas, 1986, Boehert, 1986, 1987, 1988). A. Andrijashev (1979) and N.Parin (1982) showed that seamounts form a specific ecological zone, "bathyal without a shelf" or talassobathyalzone, where various organisms can be concentrated, including benthic and pelagic ecological groups. The commonattributes of ichthyofauna on seamounts and in surrounding waters is determined by geographical zone and otherfeatures, including distance from continents, islands and other seamounts, current systems,, water depth at the top,area of the seamount, absence of a shelf, and weak development of the benthos.Talassobathyal faunal communities develop by means of drift of larvae and pelagic juveniles in nearsurface currents.All abundant talassobathyal fishes have a pelagic stage in their ontogeny that can last a number of years. During thepelagic period, juvenile talassobathyal fishes serve as prey resources. They concentrate on seamounts only at uponattaining sexual maturity.Most Northwestern and Central Pacific seamounts are located within the limits of subtropical circulation and easternPacific seamounts, as far as the Emperor and Hawaiian Seamounts, are populated on with Indo-West Pacific fauna.The distribution of benthonic representatives of this fauna further to the east is limited by interference by movementof quasi-meridional waters (Kozlov, 1971) and absence of large seamounts to the east. Southeast Pacific seamountsare located within the limits of northeast subarctic circulation and their fauna are typical of continental slopes of thesubarctic region, northern seamounts of the Emperor Ridge, and Oregon. In the productive eddy-like zones aboveseamounts, high concentrations of epi- and mesopelagic fishes and even pulses of the neritic species, such asmackerel and sardine, are formed.We report on ichthyofauna from the Emperor, Hawaiian, Kyushu-Palau, Bonin and Gulf of Alaska seamounts, aswell as some oceanographic features near these different seamounts.201
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Keynote AddressPICES XIIISend out t
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14:50-15:10 Coffee break15:10-15:30
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PICES XIII S1-1827 PosterThe red fl
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PICES XIII S1-2018 InvitedRelation
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PICES XIII S1-2049 InvitedZooplankt
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forage base while physical gradient
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S2BIO Topic SessionMechanisms that
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09:20-09:40 Rubén Rodríguez-Sánc
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PICES XIII S2-1852 OralMechanisms o
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PICES XIII S2-2003 OralTop-down mod
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espectively, several lines of evide
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PICES XIII S2-1939 InvitedWhy do om
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S3BIO Topic SessionRole of gelatino
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PICES XIII S3-1824 OralPredation on
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PICES XIII S3-1908 PosterSeasonal d
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stable-isotope ratios of carbon and
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PICES XIII S3-1930 OralA comparison
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S4FIS/BIO Topic SessionHot spots an
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17:00-17:20 Vincent F. Gallucci and
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PICES XIII S4-1983 OralExistence of
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the coast to 200 km offshore. More
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PICES XIII S4-1913 InvitedHow to di
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PICES XIII S4-2046 OralIdentifying
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PICES XIII S4-1797 PosterZone of
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S5MEQ Topic SessionIntroductions of
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PICES XIII S5-1777 OralAnthropogeni
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PICES XIII S5-2178 OralThe Ballast
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Pseudo-nitzschia, causative organis
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PICES XIII S6-2203 OralMethods for
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S7POC/MONITOR Topic SessionApplicat
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PostersYury N. Volkov, Igor E. Koch
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PICES XIII S7-1801 OralEl Niño phe
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PICES XIII S7-2189 PosterMain effec
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almost constant over the whole year
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overestimation of chl-a in the Beri
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PICES XIII S7-2196 PosterInterannua
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S8POC Topic SessionThe impacts of c
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PostersAndrey G. Andreev and Viktor
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the Pacific Ocean. Analyses of the
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PICES XIII S8-1834 OralAttributing
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will report results of a workshop c
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PICES XIII S8-2047 InvitedMicrobial
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PICES XIII S8-2140 OralInterannual
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salinity showed similar distributio
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S9CCCC Topic SessionThe impacts of
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13:50-14:10 Randall M. Peterman, Br
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PICES XIII S9-1900 OralComparison o
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PICES XIII S9-1931 OralU.S. GLOBEC:
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PICES XIII S9-1807 OralDid regime s
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depth ranges are computed for summe
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PICES XIII S9-2131 OralA new intern
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PICES XIII S9-1894 OralThe latitudi
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Southern Oscillation Index) were of
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PICES XIII S9-1789 OralPopulation d
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PICES XIII S9-2076 OralProgresses a
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PICES XIII S9-2108 OralThe importan
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PICES XIII S9-1968 OralInterannual
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PICES XIII S9-1871 OralChanging oce
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PostersIrina V. IshmukovaAssessing
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PICES XIII S10-2041 OralQuantifying
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PICES XIII S10-2083 PosterModeling
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phytoplankton growth throughout the
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W5 Workshop AbstractsPICES XIII W5-
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PICES XIII W5-2193 OralUse of Korea
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HAB Meeting AbstractsPICES XIII HAB
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PICES XIII HAB-2039 OralThe use of
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W6MBM-AP WorkshopCombining data set
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PICES XIII W6-1973 OralDistribution
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Index of AuthorsPresenter Name: Pap
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DDagg, Michael S3-1979 p.33Daly, El
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IIanson, Debby S8-2147 p.104Ichihar
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Kruse, Gordon H. FIS_P-1873 p.182S2
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Nagasawa, Toru FIS_P-1922 p.175Naka
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Samko, Eugene V. S4-1815 p.53Samuel
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Vinnikov, Andrey V. FIS_P-2088 p.18
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PICES AcronymsAP Advisory PanelAPN