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    Replacement of fish oil with vegetable oil blends in feeds for greater amberjack (Seriola dumerili) juveniles: effect on growth performance, feed efficiency, tissue fatty acid composition and flesh nutritional value

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    [EN] This study was undertaken to assess the effects of fish oil (FO) substitution by a mixture of alternative vegetable oils (VO) on Seriola dumerili culture performance. A 154-day feeding experiment was conducted using juveniles (39.2 +/- 1.6g average weight). Three isolipidic and isoenergetic meal-based diets were formulated varying their lipid component. The control diet contained 100% FO (FO100), whereas diets VO50 and VO100 included 1/2 of oil blend and all the oil from blend of palm oil (PO) and linseed oil (LO) as substitute for FO, respectively. Dietary regime did not significantly affect growth performance, biometric indices, feed efficiency, plasma chemistry and liver and muscle lipid contents. Nonetheless, dietary VO inclusion impacted on the fatty acid profile of target tissues, especially in the liver. Fatty acid profiles of the fillets reflected those of the dietary oils except that there was apparent selective utilization of palmitic acid (C16:0) and oleic acid (C18:1n-9) and apparent selective retention of long-chain polyunsaturated fatty acids, especially eicosapentaenoic acid (EPA, C20:5n-3) and docosahexaenoic acid (DHA, C22:6n-3). The nutritional value and the potential ability to prevent the development of coronary heart diseases of the flesh lipid fraction decreased with gradual FO substitution.Ministerio de Ciencia e Innovacion (MICINN), Grant/Award Number: AGL2011-30547-C03-02Monge-Ortiz, R.; Tomas-Vidal, A.; Rodriguez-Barreto, D.; Martínez-Llorens, S.; Perez, J.; Jover Cerda, M.; Lorenzo, A. (2018). Replacement of fish oil with vegetable oil blends in feeds for greater amberjack (Seriola dumerili) juveniles: effect on growth performance, feed efficiency, tissue fatty acid composition and flesh nutritional value. Aquaculture Nutrition. 24(1):605-615. https://doi.org/10.1111/anu.12595S605615241Abrami, G., Natiello, F., Bronzi, P., McKenzie, D., Bolis, L., & Agradi, E. (1992). A comparison of highly unsaturated fatty acid levels in wild and farmed eels (Anguilla Anguilla). Comparative Biochemistry and Physiology Part B: Comparative Biochemistry, 101(1-2), 79-81. doi:10.1016/0305-0491(92)90161-jAlves Martins, D., Rocha, F., Martínez-Rodríguez, G., Bell, G., Morais, S., Castanheira, F., … Conceição, L. E. C. (2011). Teleost fish larvae adapt to dietary arachidonic acid supply through modulation of the expression of lipid metabolism and stress response genes. British Journal of Nutrition, 108(5), 864-874. doi:10.1017/s0007114511006143Bell, J. G., McEvoy, J., Tocher, D. R., McGhee, F., Campbell, P. J., & Sargent, J. R. (2001). Replacement of Fish Oil with Rapeseed Oil in Diets of Atlantic Salmon (Salmo salar) Affects Tissue Lipid Compositions and Hepatocyte Fatty Acid Metabolism. The Journal of Nutrition, 131(5), 1535-1543. doi:10.1093/jn/131.5.1535Bell, J. G., McGhee, F., Campbell, P. J., & Sargent, J. R. (2003). Rapeseed oil as an alternative to marine fish oil in diets of post-smolt Atlantic salmon (Salmo salar): changes in flesh fatty acid composition and effectiveness of subsequent fish oil «wash out». Aquaculture, 218(1-4), 515-528. doi:10.1016/s0044-8486(02)00462-3Bell, J. G., & Sargent, J. R. (2003). Arachidonic acid in aquaculture feeds: current status and future opportunities. Aquaculture, 218(1-4), 491-499. doi:10.1016/s0044-8486(02)00370-8Bell, J. G., Tocher, D. R., Henderson, R. J., Dick, J. R., & Crampton, V. O. (2003). Altered Fatty Acid Compositions in Atlantic Salmon (Salmo salar) Fed Diets Containing Linseed and Rapeseed Oils Can Be Partially Restored by a Subsequent Fish Oil Finishing Diet. The Journal of Nutrition, 133(9), 2793-2801. doi:10.1093/jn/133.9.2793Benedito-Palos, L., Navarro, J. C., Sitjà-Bobadilla, A., Gordon Bell, J., Kaushik, S., & Pérez-Sánchez, J. (2008). High levels of vegetable oils in plant protein-rich diets fed to gilthead sea bream (Sparus aurata L.): growth performance, muscle fatty acid profiles and histological alterations of target tissues. British Journal of Nutrition, 100(5), 992-1003. doi:10.1017/s0007114508966071Benedito-Palos, L., Saera-Vila, A., Calduch-Giner, J.-A., Kaushik, S., & Pérez-Sánchez, J. (2007). Combined replacement of fish meal and oil in practical diets for fast growing juveniles of gilthead sea bream (Sparus aurata L.): Networking of systemic and local components of GH/IGF axis. Aquaculture, 267(1-4), 199-212. doi:10.1016/j.aquaculture.2007.01.011BOURAOUI, L., SÁNCHEZ-GURMACHES, J., CRUZ-GARCIA, L., GUTIÉRREZ, J., BENEDITO-PALOS, L., PÉREZ-SÁNCHEZ, J., & NAVARRO, I. (2010). Effect of dietary fish meal and fish oil replacement on lipogenic and lipoprotein lipase activities and plasma insulin in gilthead sea bream (Sparus aurata). Aquaculture Nutrition, 17(1), 54-63. doi:10.1111/j.1365-2095.2009.00706.xBowyer, J. N., Qin, J. G., Smullen, R. P., Adams, L. R., Thomson, M. J. S., & Stone, D. A. J. (2013). The use of a soy product in juvenile yellowtail kingfish (Seriola lalandi) feeds at different water temperatures: 1. Solvent extracted soybean meal. Aquaculture, 384-387, 35-45. doi:10.1016/j.aquaculture.2012.12.005Bowyer, J. N., Qin, J. G., Smullen, R. P., & Stone, D. A. J. (2012). Replacement of fish oil by poultry oil and canola oil in yellowtail kingfish (Seriola lalandi) at optimal and suboptimal temperatures. Aquaculture, 356-357, 211-222. doi:10.1016/j.aquaculture.2012.05.014Bowyer, J. N., Rout-Pitt, N., Bain, P. A., Stone, D. A. J., & Schuller, K. A. (2012). 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R., JEREZ, S., LORENZO, A., & RODRÍGUEZ, C. (2009). Effect of dietary substitution of fish oil byEchiumoil on growth, plasma parameters and body lipid composition in gilthead seabream (Sparus aurataL.). Aquaculture Nutrition, 15(5), 500-512. doi:10.1111/j.1365-2095.2008.00616.xFountoulaki, E., Vasilaki, A., Hurtado, R., Grigorakis, K., Karacostas, I., Nengas, I., … Alexis, M. N. (2009). Fish oil substitution by vegetable oils in commercial diets for gilthead sea bream (Sparus aurata L.); effects on growth performance, flesh quality and fillet fatty acid profile. Aquaculture, 289(3-4), 317-326. doi:10.1016/j.aquaculture.2009.01.023Gisbert, E., Giménez, G., Fernández, I., Kotzamanis, Y., & Estévez, A. (2009). Development of digestive enzymes in common dentex Dentex dentex during early ontogeny. Aquaculture, 287(3-4), 381-387. doi:10.1016/j.aquaculture.2008.10.039Glencross, B. D. (2009). Exploring the nutritional demand for essential fatty acids by aquaculture species. 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Effect of dietary canola oil level on the growth performance and fatty acid composition of juvenile red sea bream, Pagrus major. Aquaculture, 271(1-4), 420-431. doi:10.1016/j.aquaculture.2007.06.004Izquierdo, M. S., Obach, A., Arantzamendi, L., Montero, D., Robaina, L., & Rosenlund, G. (2003). Dietary lipid sources for seabream and seabass: growth performance, tissue composition and flesh quality. Aquaculture Nutrition, 9(6), 397-407. doi:10.1046/j.1365-2095.2003.00270.xKaushik, S. J., Covès, D., Dutto, G., & Blanc, D. (2004). Almost total replacement of fish meal by plant protein sources in the diet of a marine teleost, the European seabass, Dicentrarchus labrax. Aquaculture, 230(1-4), 391-404. doi:10.1016/s0044-8486(03)00422-8Khankari, N. K., Bradshaw, P. T., Steck, S. E., He, K., Olshan, A. F., Shen, J., … Gammon, M. D. (2015). Dietary intake of fish, polyunsaturated fatty acids, and survival after breast cancer: A population-based follow-up study on Long Island, New York. Cancer, 121(13), 2244-2252. doi:10.1002/cncr.29329Khaoian, P., Nguyen, H. P., Ogita, Y., Fukada, H., & Masumoto, T. (2014). Taurine supplementation and palm oil substitution in low-fish meal diets for young yellowtail Seriola quinqueradiata. Aquaculture, 420-421, 219-224. doi:10.1016/j.aquaculture.2013.11.012Kiessling, K.-H., & Kiessling, A. (1993). Selective utilization of fatty acids in rainbow trout (Oncorhynchus mykiss Walbaum) red muscle mitochondria. Canadian Journal of Zoology, 71(2), 248-251. doi:10.1139/z93-035Kowalska, A., Zakęś, Z., Siwicki, A. K., Jankowska, B., Jarmołowicz, S., & Demska-Zakęś, K. (2011). Impact of diets with different proportions of linseed and sunflower oils on the growth, liver histology, immunological and chemical blood parameters, and proximate composition of pikeperch Sander lucioperca (L.). Fish Physiology and Biochemistry, 38(2), 375-388. doi:10.1007/s10695-011-9514-zLech, G. P., & Reigh, R. C. (2012). Plant Products Affect Growth and Digestive Efficiency of Cultured Florida Pompano (Trachinotus carolinus) Fed Compounded Diets. PLoS ONE, 7(4), e34981. doi:10.1371/journal.pone.0034981Lemaire, P., Drai, P., Mathieu, A., Lemaire, S., Carrière, S., Giudicelli, J., & Lafaurie, M. (1991). Changes with different diets in plasma enzymes (GOT, GPT, LDH, ALP) and plasma lipids (cholesterol, triglycerides) of sea-bass (Dicentrarchus labrax). Aquaculture, 93(1), 63-75. doi:10.1016/0044-8486(91)90205-lLin, H., Chen, X., Chen, S., Zhuojia, L., Huang, Z., Niu, J., … Lu, X. (2011). Replacement of fish meal with fermented soybean meal in practical diets for pompanoTrachinotus ovatus. Aquaculture Research, 44(1), 151-156. doi:10.1111/j.1365-2109.2011.03000.xMazzola, A., Favaloro, E., & Sarà, G. (2000). Cultivation of the Mediterranean amberjack, Seriola dumerili (Risso, 1810), in submerged cages in the Western Mediterranean Sea. 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Partial or total replacement of dietary fish oil with alternative lipid sources in silvery-black porgy (Sparidentex hasta). Aquaculture, 451, 232-240. doi:10.1016/j.aquaculture.2015.09.022Nguyen, H. P., Khaoian, P., Fukada, H., Suzuki, N., & Masumoto, T. (2013). Feeding fermented soybean meal diet supplemented with taurine to yellowtailSeriola quinqueradiataaffects growth performance and lipid digestion. Aquaculture Research, 46(5), 1101-1110. doi:10.1111/are.12267Peng, S., Chen, L., Qin, J. G., Hou, J., Yu, N., Long, Z., … Sun, X. (2008). Effects of replacement of dietary fish oil by soybean oil on growth performance and liver biochemical composition in juvenile black seabream, Acanthopagrus schlegeli. Aquaculture, 276(1-4), 154-161. doi:10.1016/j.aquaculture.2008.01.035Pérez, J. A., Rodríguez, C., Bolaños, A., Cejas, J. R., & Lorenzo, A. (2014). 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    Ultraviolet-Optical observations of the Seyfert 2 Galaxies NGC 7130, NGC 5135 and IC 3639: Implications for the Starburst-AGN Connection

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    We present and discuss HST (WFPC2 and FOC) images and UV GHRS spectra plus ground-based near UV through to near IR spectra of three Seyfert 2 nuclei (NGC 7130, NGC 5135 and IC 3639). These galaxies, together to Mrk 477, were selected from a bigger sample that comprises the 20 brightest Seyfert 2 nuclei, with the goal to study the origin of the UV-optical-near IR featureless continuum in Seyfert 2 nuclei. These four galaxies have bolometric luminosities, as computed with the four IRAS bands, of 10^11 Lsol. They are close enough to be resolved with HST the nuclear zone. This makes these Seyfert 2 galaxies benchmarks to study the Starburst-AGN connection in more distant galaxies. The data provide direct evidence of the existence of a central nuclear starburst that dominates the UV light, and that seem to be responsible for the origin of the so called featureless continuum. These starbursts are dusty and compact. They have sizes (from less than 100 pc to a few hundred pc) much smaller and closer to the nucleus than that seen in the prototype Seyfert 2 galaxy NGC 1068. The bolometric luminosity of these starbursts is similar to the estimated bolometric luminosities of their obscured Seyfert 1 nuclei, and thus they contribute in the same amount to the overall energetics of these galaxies.Comment: to be published in ApJ 505, September issue. The figures are in a tar files at: http://www.iaa.es/~rosa/Seyfert

    Transcriptomic response to aquaculture intensification in Nile tilapia

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    To meet future global demand for fish protein, more fish will need to be farmed usingfewer resources, and this will require the selection of nonaggressive individuals thatperform well at high densities. Yet, the genetic changes underlying loss of aggressionand adaptation to crowding during aquaculture intensification are largely unknown.We examined the transcriptomic response to aggression and crowding in Nile tilapia,one of the oldest and most widespread farmed fish, whose social structure shiftsfrom social hierarchies to shoaling with increasing density. A mirror test was usedto quantify aggression and skin darkening (a proxy for stress) of fish reared at lowand high densities, and gene expression in the hypothalamus was analysed amongthe most and least aggressive fish at each density. Fish reared at high density weredarker, had larger brains, were less active and less aggressive than those reared atlow density and had differentially expressed genes consistent with a reactive stress-copingstyle and activation of the hypothalamus–pituitary–interrenal (HPI) axis.Differences in gene expression among aggressive fish were accounted for by densityand the interaction between density and aggression levels, whereas for non-aggressivefish differences in gene expression were associated with individual variation inskin brightness and social stress. Thus, the response to crowding in Nile tilapia iscontext dependent and involves different neuro-endocrine pathways, depending onsocial status. Knowledge of genes associated with the response to crowding maypave the way for more efficient fish domestication, based on the selection of non-aggressiveindividuals with increasing tolerance to chronic stress necessary for aquacultureintensification

    Search for the standard model Higgs boson decaying to a bbˉb\bar{b} pair in events with no charged leptons and large missing transverse energy using the full CDF data set

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    We report on a search for the standard model Higgs boson produced in association with a vector boson in the full data set of proton-antiproton collisions at s=1.96\sqrt{s} = 1.96 TeV recorded by the CDF II detector at the Tevatron, corresponding to an integrated luminosity of 9.45 fb1^{-1}. We consider events having no identified charged lepton, a transverse energy imbalance, and two or three jets, of which at least one is consistent with originating from the decay of a bb quark. We place 95% credibility level upper limits on the production cross section times standard model branching fraction for several mass hypotheses between 90 and 150GeV/c2150 \mathrm{GeV}/c^2. For a Higgs boson mass of 125GeV/c2125 \mathrm{GeV}/c^2, the observed (expected) limit is 6.7 (3.6) times the standard model prediction.Comment: Accepted by Phys. Rev. Let

    Search for the standard model Higgs boson decaying to a bb pair in events with one charged lepton and large missing transverse energy using the full CDF data set

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    We present a search for the standard model Higgs boson produced in association with a W boson in sqrt(s) = 1.96 TeV p-pbar collision data collected with the CDF II detector at the Tevatron corresponding to an integrated luminosity of 9.45 fb-1. In events consistent with the decay of the Higgs boson to a bottom-quark pair and the W boson to an electron or muon and a neutrino, we set 95% credibility level upper limits on the WH production cross section times the H->bb branching ratio as a function of Higgs boson mass. At a Higgs boson mass of 125 GeV/c2 we observe (expect) a limit of 4.9 (2.8) times the standard model value.Comment: Submitted to Phys. Rev. Lett (v2 contains clarifications suggested by PRL

    Search for the standard model Higgs boson decaying to a bb pair in events with two oppositely-charged leptons using the full CDF data set

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    We present a search for the standard model Higgs boson produced in association with a Z boson in data collected with the CDF II detector at the Tevatron, corresponding to an integrated luminosity of 9.45/fb. In events consistent with the decay of the Higgs boson to a bottom-quark pair and the Z boson to electron or muon pairs, we set 95% credibility level upper limits on the ZH production cross section times the H -> bb branching ratio as a function of Higgs boson mass. At a Higgs boson mass of 125 GeV/c^2 we observe (expect) a limit of 7.1 (3.9) times the standard model value.Comment: To be submitted to Phys. Rev. Let

    Search for chargino-neutralino production with mass splittings near the electroweak scale in three-lepton final states in √s=13 TeV pp collisions with the ATLAS detector

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    A search for supersymmetry through the pair production of electroweakinos with mass splittings near the electroweak scale and decaying via on-shell W and Z bosons is presented for a three-lepton final state. The analyzed proton-proton collision data taken at a center-of-mass energy of √s=13  TeV were collected between 2015 and 2018 by the ATLAS experiment at the Large Hadron Collider, corresponding to an integrated luminosity of 139  fb−1. A search, emulating the recursive jigsaw reconstruction technique with easily reproducible laboratory-frame variables, is performed. The two excesses observed in the 2015–2016 data recursive jigsaw analysis in the low-mass three-lepton phase space are reproduced. Results with the full data set are in agreement with the Standard Model expectations. They are interpreted to set exclusion limits at the 95% confidence level on simplified models of chargino-neutralino pair production for masses up to 345 GeV
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