231 research outputs found

    Monitoring and ming bio-physical parameters for hypoxia hazard in a coastal sand pit

    Get PDF
    Management of coastal areas requires monitoring and modeling of the anthropogenic drivers and the bio-physical processes affecting water quality. To assess the range of hydrographic conditions controlling oxygen distribution in the bottom layers of sand pits, a multi-year oceanographic survey has been conducted in a coastal area with several extraction pits. Hydrographic data including profiles of temperature, salinity and oxygen were collected and related to local wind conditions and circulation. Moreover, 1D and 3D high-resolution non-hydrostatic ocean models were used to describe turbulent mixing regimes and to obtain the range of wind speeds for which the critical anoxic conditions may occur. It is shown that wind speed appears to control the dynamics of oxygen concentrations, with oxygen depleted zones developing in a short time in low wind speed conditions. Moreover, the depth and the shape of the extraction pit contribute to decrease the mixing of the bottom layers and increase the water retention in the hole increasing the output and the persistence of oxygen depleted zones in the excavated area. The results of the numerical simulations show that the risk of hypoxia at the bottom of the sand pits is associated with higher temperatures and wind speed lower than 5 m/s, which is not infrequent during the summer season. However, the number of consecutive days of oxygen depletion can be considered lower than the danger threshold level assumed in the literature

    Dietary amino acids impact sperm performance traits for a catadromous fish, Anguilla anguilla reared in captivity

    Full text link
    Systematic reproduction and distribution, duplication of any material in this paper for a fee or for commercial purposes, or modifications of the content of this paper are prohibited.[EN] Little is known about the role of dietary amino acids on male reproductive performance and gamete quality in fishes. Thus, the objective of this study was to investigate how "enhanced" feeds (EH-4, EH-5, EH-6), with modified amino acid composition, and the standard on-growing diet (DAN-EX) impact body composition, milt biochemistry, and sperm performance in male European eel, Anguilla anguilla. The fatty acid composition of EH4, EH-5, and EH-6 was similar but differed to that in DAN-EX, while amino acid composition varied between all four diets. Diet did not influence organ-somatic indices (e.g. HSI, GSI), while males fed EH-4 were heavier than other groups. Arginine, alanine, and lysine were the most abundant amino acids in milt (>11%), followed by glycine, aspartic acid, valine, glutamic acid, and leucine ( >5.66%). Diet impacted milt arginine, serine, proline, methionine, and histidine levels. Specifically, males fed DAN-EX, EH-4, and EH-5 had the highest percentages of arginine, while males fed EH-4 to EH-6 had higher percentages of serine. Proline was most abundant in males fed DAN-EX, EH-5, and EH-6. Both methionine and histidine were detected at low percentages ( 0.5 mL) for fertilization procedures. Spermatocrit (43.1 +/- 1.80%) did not differ between the diets (ranged from 37.57 to 47.21%). Dietary regime had an impact on sperm motility, such that eels fed EH-5 and EH-6 had the greatest percentage of motile cells. In addition, fish fed EH-5 and EH-6 (or DAN-EX) had the fastest swimming sperm. Spermatogenic maturity index of hormonally treated eels varied within groups but did not differ between dietary treatment groups after 9 weeks of injections (ranged from 0.54 to 0.80). The most interesting amino acids to scrutinize from PCA plots were proline, histidine, and valine as well as lysine and arginine. Here, eels with highly motile sperm had milt with high relative proportions of proline, histidine, and valine, but were particularly low in lysine and arginine. Together, our findings add evidence that certain amino acids regulate milt biochemistry, and that male ejaculate traits may be promoted by amino acid intake. Further studies to evaluate effects of supplemented amino acid diets on fertilization ability and inter-linked early developmental stages are required.This study was funded by the Innovation Fund Denmark under grant agreements no. 5184-00093B (EEL-HATCH) and 7076-00125B (ITSEEL). Butts IAE, was also supported by the USDA National Institute of Food and Agriculture, Hatch project 1013854. Gallego V has a post-doc grant from the MICIU (Juan de la Cierva-Incorporacion; IJCI-201734200).Butts, IAE.; Hilmarsdóttir, GS.; Zadmajid, V.; Gallego Albiach, V.; Stottrup, JG.; Jacobsen, C.; Krüger-Johnsen, M.... (2020). Dietary amino acids impact sperm performance traits for a catadromous fish, Anguilla anguilla reared in captivity. Aquaculture. 518:1-12. https://doi.org/10.1016/j.aquaculture.2019.734602112518Abd-Elrazek, A. M., & Ahmed-Farid, O. A. H. (2017). Protective effect of L-carnitine and L-arginine against busulfan-induced oligospermia in adult rat. Andrologia, 50(1), e12806. doi:10.1111/and.12806Akiyama, T., Shiraishi, M., Yamamoto, T., & Unuma, T. (1996). Effect of Dietary Tryptophan on Maturation of Ayu Plecoglossus altivelis. Fisheries science, 62(5), 776-782. doi:10.2331/fishsci.62.776Alavi, S. M. H., Pšenička, M., Policar, T., Rodina, M., Hamáčková, J., Kozák, P., & Linhart, O. (2009). Sperm quality in male Barbus barbus L. fed different diets during the spawning season. Fish Physiology and Biochemistry, 35(4), 683-693. doi:10.1007/s10695-009-9325-7Asturiano, J. F., Sorbera, L. A., Carrillo, M., Zanuy, S., Ramos, J., Navarro, J. C., & Bromage, N. (2001). Reproductive performance in male European sea bass (Dicentrarchus labrax, L.) fed two PUFA-enriched experimental diets: a comparison with males fed a wet diet. Aquaculture, 194(1-2), 173-190. doi:10.1016/s0044-8486(00)00515-9Asturiano, J. F., Perez, L., Garzon, D. L., Penaranda, D. S., Marco-Jimenez, F., Martinez-Llorens, S., … Jover, M. (2005). Effect of different methods for the induction of spermiation on semen quality in European eel. Aquaculture Research, 36(15), 1480-1487. doi:10.1111/j.1365-2109.2005.01366.xBaeza, R., Mazzeo, I., Vílchez, M. C., Gallego, V., Peñaranda, D. S., Pérez, L., & Asturiano, J. F. (2014). Effect of thermal regime on fatty acid dynamics in male European eels (Anguilla anguilla) during hormonally-induced spermatogenesis. Aquaculture, 430, 86-97. doi:10.1016/j.aquaculture.2014.03.045Baeza, R., Mazzeo, I., Vílchez, M. C., Gallego, V., Peñaranda, D. S., Pérez, L., & Asturiano, J. F. (2015). Relationship between sperm quality parameters and the fatty acid composition of the muscle, liver and testis of European eel. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 181, 79-86. doi:10.1016/j.cbpa.2014.11.022Baeza, R., Peñaranda, D. S., Vílchez, M. C., Tveiten, H., Pérez, L., & Asturiano, J. F. (2015). Exploring correlations between sex steroids and fatty acids and their potential roles in the induced maturation of the male European eel. Aquaculture, 435, 328-335. doi:10.1016/j.aquaculture.2014.10.016Bahadorani, M., Tavalaee, M., Abedpoor, N., Ghaedi, K., Nazem, M. N., & Nasr-Esfahani, M. H. (2018). Effects of branched-chain amino acid supplementation and/or aerobic exercise on mouse sperm quality and testosterone production. Andrologia, 51(2), e13183. doi:10.1111/and.13183Beirão, J., Soares, F., Pousão-Ferreira, P., Diogo, P., Dias, J., Dinis, M. T., … Cabrita, E. (2015). The effect of enriched diets on Solea senegalensis sperm quality. Aquaculture, 435, 187-194. doi:10.1016/j.aquaculture.2014.09.025Benini, E., Politis, S. N., Kottmann, J. S., Butts, I. A. E., Sørensen, S. R., & Tomkiewicz, J. (2018). Effect of parental origin on early life history traits of European eel. Reproduction in Domestic Animals, 53(5), 1149-1158. doi:10.1111/rda.13219Barman, A. S., Kumar, P., Mariahabib, Lal, K. K., & Lal, B. (2013). Role of nitric oxide in motility and fertilizing ability of sperm of Heteropneustes fossilis (Bloch.). Animal Reproduction Science, 137(1-2), 119-127. doi:10.1016/j.anireprosci.2012.12.001Bromage, N., Jones, J., Randall, C., Thrush, M., Davies, B., Springate, J., … Barker, G. (1992). Broodstock management, fecundity, egg quality and the timing of egg production in the rainbow trout (Oncorhynchus mykiss). Aquaculture, 100(1-3), 141-166. doi:10.1016/0044-8486(92)90355-oBuentello, J. A., & Gatlin, D. M. (2001). Effects of Elevated Dietary Arginine on Resistance of Channel Catfish to Exposure toEdwardsiella ictaluri. Journal of Aquatic Animal Health, 13(3), 194-201. doi:10.1577/1548-8667(2001)0132.0.co;2Butts, I. A. E., Baeza, R., Støttrup, J. G., Krüger-Johnsen, M., Jacobsen, C., Pérez, L., … Tomkiewicz, J. (2015). Impact of dietary fatty acids on muscle composition, liver lipids, milt composition and sperm performance in European eel. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 183, 87-96. doi:10.1016/j.cbpa.2015.01.015Cabrita, E., Ma, S., Diogo, P., Martínez-Páramo, S., Sarasquete, C., & Dinis, M. T. (2011). The influence of certain aminoacids and vitamins on post-thaw fish sperm motility, viability and DNA fragmentation. Animal Reproduction Science, 125(1-4), 189-195. doi:10.1016/j.anireprosci.2011.03.003Cabrita, E., Martínez-Páramo, S., Gavaia, P. J., Riesco, M. F., Valcarce, D. G., Sarasquete, C., … Robles, V. (2014). Factors enhancing fish sperm quality and emerging tools for sperm analysis. Aquaculture, 432, 389-401. doi:10.1016/j.aquaculture.2014.04.034Ciereszko, A., Piros, B., Dabrowski, K., Kucharczyk, D., Luczynski, M. J., Dobosz, S., & Glogowski, J. (1998). Serine proteinase inhibitors of seminal plasma of teleost fish: distribution of activity, electrophoretic profiles and relation to proteinase inhibitors of blood. Journal of Fish Biology, 53(6), 1292-1305. doi:10.1111/j.1095-8649.1998.tb00249.xDabrowski, K., Luczynski, M., & Rusiecki, M. (1985). Free amino acids in the late embryogenesis and pre-hatching stage of two coregonid fishes. Biochemical Systematics and Ecology, 13(3), 349-356. doi:10.1016/0305-1978(85)90048-1Da Silva, F. F. G., Støttrup, J. G., Kjørsvik, E., Tveiten, H., & Tomkiewicz, J. (2016). Interactive effects of dietary composition and hormonal treatment on reproductive development of cultured female European eel, Anguilla anguilla. Animal Reproduction Science, 171, 17-26. doi:10.1016/j.anireprosci.2016.05.007F.G. da Silva, F., Jacobsen, C., Kjørsvik, E., G. Støttrup, J., & Tomkiewicz, J. (2018). Oocyte and egg quality indicators in European eel: Lipid droplet coalescence and fatty acid composition. Aquaculture, 496, 30-38. doi:10.1016/j.aquaculture.2018.07.008Diemer, O., Bittencourt, F., Barcellos, L. G., Boscolo, W. R., Feiden, A., & Romagosa, E. (2014). Lysine in the diet of Rhamdia voulezi male broodstocks confined in net cages. Aquaculture, 434, 93-99. doi:10.1016/j.aquaculture.2014.07.029Dong, H.-J., Wu, D., Xu, S.-Y., Li, Q., Fang, Z.-F., Che, L.-Q., … Lin, Y. (2016). Effect of dietary supplementation with amino acids on boar sperm quality and fertility. Animal Reproduction Science, 172, 182-189. doi:10.1016/j.anireprosci.2016.08.003Dzyuba, V., & Cosson, J. (2014). Motility of fish spermatozoa: from external signaling to flagella response. Reproductive Biology, 14(3), 165-175. doi:10.1016/j.repbio.2013.12.005Finn, R. N., & Fyhn, H. J. (2010). Requirement for amino acids in ontogeny of fish. Aquaculture Research, 41(5), 684-716. doi:10.1111/j.1365-2109.2009.02220.xForster, I., & Ogata, H. Y. (1998). Lysine requirement of juvenile Japanese flounder Paralichthys olivaceus and juvenile red sea bream Pagrus major. Aquaculture, 161(1-4), 131-142. doi:10.1016/s0044-8486(97)00263-9Gallego, V., Mazzeo, I., Vílchez, M. C., Peñaranda, D. S., Carneiro, P. C. F., Pérez, L., & Asturiano, J. F. (2012). Study of the effects of thermal regime and alternative hormonal treatments on the reproductive performance of European eel males (Anguilla anguilla) during induced sexual maturation. Aquaculture, 354-355, 7-16. doi:10.1016/j.aquaculture.2012.04.041Gallego, V., & Asturiano, J. F. (2018). Sperm motility in fish: technical applications and perspectives through CASA-Mot systems. Reproduction, Fertility and Development, 30(6), 820. doi:10.1071/rd17460Gallego, V., & Asturiano, J. F. (2018). Fish sperm motility assessment as a tool for aquaculture research: a historical approach. Reviews in Aquaculture, 11(3), 697-724. doi:10.1111/raq.12253He, S., & Woods III, L. . (2003). Effects of glycine and alanine on short-term storage and cryopreservation of striped bass (Morone saxatilis) spermatozoa. Cryobiology, 46(1), 17-25. doi:10.1016/s0011-2240(02)00159-1Heinsbroek, L. T. N., Støttrup, J. G., Jacobsen, C., Corraze, G., Kraiem, M. M., Holst, L. K., … Kaushik, S. J. (2013). A review on broodstock nutrition of marine pelagic spawners: the curious case of the freshwater eels (Anguillaspp.). Aquaculture Nutrition, 19, 1-24. doi:10.1111/anu.12091Higuchi, M., Celino, F. T., Tamai, A., Miura, C., & Miura, T. (2011). The synthesis and role of taurine in the Japanese eel testis. Amino Acids, 43(2), 773-781. doi:10.1007/s00726-011-1128-3Izquierdo, M. ., Fernández-Palacios, H., & Tacon, A. G. . (2001). Effect of broodstock nutrition on reproductive performance of fish. Aquaculture, 197(1-4), 25-42. doi:10.1016/s0044-8486(01)00581-6Jobgen, W. S., Fried, S. K., Fu, W. J., Meininger, C. J., & Wu, G. (2006). Regulatory role for the arginine–nitric oxide pathway in metabolism of energy substrates. The Journal of Nutritional Biochemistry, 17(9), 571-588. doi:10.1016/j.jnutbio.2005.12.001Kaushik, S. J., Fauconneau, B., Terrier, L., & Gras, J. (1988). Arginine requirement and status assessed by different biochemical indices in rainbow trout (Salmo gairdneri R.). Aquaculture, 70(1-2), 75-95. doi:10.1016/0044-8486(88)90008-7Kawabata, K., Tsubaki, K., Tazaki, T., & Ikeda, S. (1992). Sexual Behavior Induced by Amino Acids in the Rose Bitterling Rhodeus ocellatus ocellatus. NIPPON SUISAN GAKKAISHI, 58(5), 839-844. doi:10.2331/suisan.58.839Keller, D. W., & Polakoski, K. L. (1975). L-Arginine Stimulation of Human Sperm Motility in vitro. Biology of Reproduction, 13(2), 154-157. doi:10.1095/biolreprod13.2.154Kjørsvik, E., Hoehne-Reitan, K., & Reitan, K. I. (2003). Egg and larval quality criteria as predictive measures for juvenile production in turbot (Scophthalmus maximus L.). Aquaculture, 227(1-4), 9-20. doi:10.1016/s0044-8486(03)00492-7Kwasek, K., Dabrowski, K., Nynca, J., Takata, R., Wojno, M., & Wick, M. (2014). The Influence of Dietary Lysine on Yellow Perch Female Reproductive Performance and the Quality of Eggs. North American Journal of Aquaculture, 76(4), 351-358. doi:10.1080/15222055.2014.911223Kwasek, K., Dabrowski, K., Nynca, J., Wojno, M., & Wick, M. (2014). The Influence of Dietary Lysine on Yellow Perch Maturation and the Quality of Sperm. North American Journal of Aquaculture, 76(2), 119-126. doi:10.1080/15222055.2013.856826Labbe, C., Maisse, G., Müller, K., Zachowski, A., Kaushik, S., & Loir, M. (1995). Thermal acclimation and dietary lipids alter the composition, but not fluidity, of trout sperm plasma membrane. Lipids, 30(1), 23-33. doi:10.1007/bf02537038Lahnsteiner, F., Patzner, R. A., & Welsmann, T. (1993). The spermatic ducts of salmonid fishes (Salmonidae, Teleostei). Morphology, histochemistry and composition of the secretion. Journal of Fish Biology, 42(1), 79-93. doi:10.1111/j.1095-8649.1993.tb00307.xLahnsteiner, F. (2009). The role of free amino acids in semen of rainbow troutOncorhynchus mykissand carpCyprinus carpio. Journal of Fish Biology, 75(4), 816-833. doi:10.1111/j.1095-8649.2009.02317.xLahnsteiner, F., Mansour, N., McNiven, M. A., & Richardson, G. F. (2009). Fatty acids of rainbow trout (Oncorhynchus mykiss) semen: Composition and effects on sperm functionality. Aquaculture, 298(1-2), 118-124. doi:10.1016/j.aquaculture.2009.08.034Lahnsteiner, F. (2010). A comparative study on the composition and importance of free amino acids in semen of gilthead sea bream, Sparus aurata, and perch, Perca fluviatilis. Fish Physiology and Biochemistry, 36(4), 1297-1305. doi:10.1007/s10695-010-9442-3Li, P., Mai, K., Trushenski, J., & Wu, G. (2008). New developments in fish amino acid nutrition: towards functional and environmentally oriented aquafeeds. Amino Acids, 37(1), 43-53. doi:10.1007/s00726-008-0171-1Mai, K., Lu Zhang, Ai, Q., Duan, Q., Zhang, C., Li, H., … Liufu, Z. (2006). Dietary lysine requirement of juvenile Japanese seabass, Lateolabrax japonicus. Aquaculture, 258(1-4), 535-542. doi:10.1016/j.aquaculture.2006.04.043Mansour, N., McNiven, M. A., & Richardson, G. F. (2006). The effect of dietary supplementation with blueberry, α-tocopherol or astaxanthin on oxidative stability of Arctic char (Salvelinus alpinus) semen. Theriogenology, 66(2), 373-382. doi:10.1016/j.theriogenology.2005.12.002Martinage, A., Gusse, M., Bélaïche, D., Sautière, P., & Chevaillier, P. (1985). Amino acid sequence of a cysteine-rich, arginine-rich sperm protamine of the dog-fish Scylliorhinus caniculus. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 831(2), 172-178. doi:10.1016/0167-4838(85)90032-9MATSUNARI, H., HAMADA, K., MUSHIAKE, K., & TAKEUCHI, T. (2006). Effects of taurine levels in broodstock diet on reproductive performance of yellowtail Seriola quinqueradiata. Fisheries Science, 72(5), 955-960. doi:10.1111/j.1444-2906.2006.01243.xMozanzadeh, M. T., Yaghoubi, M., Marammazi, J. G., Safari, O., & Gisbert, E. (2018). Effects of dietary protein and essential amino acid deficiencies on growth, body composition, and digestive enzyme activities of silvery-black porgy (Sparidentex hasta). International Aquatic Research, 10(1), 45-55. doi:10.1007/s40071-017-0187-9Mylonas, C. C., Duncan, N. J., & Asturiano, J. F. (2017). Hormonal manipulations for the enhancement of sperm production in cultured fish and evaluation of sperm quality. Aquaculture, 472, 21-44. doi:10.1016/j.aquaculture.2016.04.021Nandi, S., Routray, P., Gupta, S. D., Rath, S. C., Dasgupta, S., Meher, P. K., & Mukhopadhyay, P. K. (2007). Reproductive performance of carp, Catla catla (Ham.), reared on a formulated diet with PUFA supplementation. Journal of Applied Ichthyology, 23(6), 684-691. doi:10.1111/j.1439-0426.2007.00874.xPatel, A. B., Srivastava, S., Phadke, R. S., & Govil, G. (1998). Arginine Activates Glycolysis of Goat Epididymal Spermatozoa: An NMR Study. Biophysical Journal, 75(3), 1522-1528. doi:10.1016/s0006-3495(98)74071-8Peñaranda, D. S., Pérez, L., Gallego, V., Jover, M., Tveiten, H., Baloche, S., … Asturiano, J. F. (2010). Molecular and physiological study of the artificial maturation process in European eel males: From brain to testis. General and Comparative Endocrinology, 166(1), 160-171. doi:10.1016/j.ygcen.2009.08.006Poupard, G. P., Paxion, C., Cosson, J., Jeulin, C., Fierville, F., & Billard, R. (1998). Initiation of carp spermatozoa motility and early ATP reduction after milt contamination by urine. Aquaculture, 160(3-4), 317-328. doi:10.1016/s0044-8486(97)00301-3Perez, L., Aturiano, J. F., Tomas, A., Zegrari, S., Barrera, R., Espinos, F. J., … Jover, M. (2000). Induction of maturation and spermiation in the male European eel: assessment of sperm quality throughout treatment. Journal of Fish Biology, 57(6), 1488-1504. doi:10.1111/j.1095-8649.2000.tb02227.xPolitis, S. N., Mazurais, D., Servili, A., Zambonino-Infante, J.-L., Miest, J. J., Sørensen, S. R., … Butts, I. A. E. (2017). Temperature effects on gene expression and morphological development of European eel, Anguilla anguilla larvae. PLOS ONE, 12(8), e0182726. doi:10.1371/journal.pone.0182726Politis, S. N., Mazurais, D., Servili, A., Zambonino-Infante, J.-L., Miest, J. J., Tomkiewicz, J., & Butts, I. A. E. (2018). Salinity reduction benefits European eel larvae: Insights at the morphological and molecular level. PLOS ONE, 13(6), e0198294. doi:10.1371/journal.pone.0198294Politis, S. N., Servili, A., Mazurais, D., Zambonino-Infante, J.-L., Miest, J. J., Tomkiewicz, J., & Butts, I. A. E. (2018). Temperature induced variation in gene expression of thyroid hormone receptors and deiodinases of European eel (Anguilla anguilla) larvae. General and Comparative Endocrinology, 259, 54-65. doi:10.1016/j.ygcen.2017.11.003Politis, S. N., Sørensen, S. R., Mazurais, D., Servili, A., Zambonino-Infante, J.-L., Miest, J. J., … Butts, I. A. E. (2018). Molecular Ontogeny of First-Feeding European Eel Larvae. Frontiers in Physiology, 9. doi:10.3389/fphys.2018.01477Pourkhazaei, F., Ebrahimi, E., & Ghaedi, A. (2016). Arginine effects on biochemical composition of sperm in rainbow trout, Oncorhynchus mykiss. Aquaculture Research, 48(7), 3464-3471. doi:10.1111/are.13172R�nnestad, I., Fyhn, H. J., & Gravningen, K. (1992). The importance of free amino acids to the energy metabolism of eggs and larvae of turbot (Scophthalmus maximus). Marine Biology, 114(4), 517-525. doi:10.1007/bf00357249Ruchimat, T., Masumoto, T., Hosokawa, H., Itoh, Y., & Shimeno, S. (1997). Quantitative lysine requirement of yellowtail (Seriola quinqueradiata). Aquaculture, 158(3-4), 331-339. doi:10.1016/s0044-8486(97)00215-9Rurangwa, E., Kime, D. ., Ollevier, F., & Nash, J. . (2004). The measurement of sperm motility and factors affecting sperm quality in cultured fish. Aquaculture, 234(1-4), 1-28. doi:10.1016/j.aquaculture.2003.12.006Safafar, H., Hass, M., Møller, P., Holdt, S., & Jacobsen, C. (2016). High-EPA Biomass from Nannochloropsis salina Cultivated in a Flat-Panel Photo-Bioreactor on a Process Water-Enriched Growth Medium. Marine Drugs, 14(8), 144. doi:10.3390/md14080144Sangeeta, S., Arangasamy, A., Kulkarni, S., & Selvaraju, S. (2015). Role of amino acids as additives on sperm motility, plasma membrane integrity and lipid peroxidation levels at pre-freeze and post-thawed ram semen. Animal Reproduction Science, 161, 82-88. doi:10.1016/j.anireprosci.2015.08.008Silva, J. V., Freitas, M. J., Correia, B. R., Korrodi-Gregório, L., Patrício, A., Pelech, S., & Fardilha, M. (2015). Profiling signaling proteins in human spermatozoa: biomarker identification for sperm quality evaluation. Fertility and Sterility, 104(4), 845-856.e8. doi:10.1016/j.fertnstert.2015.06.039Sørensen, S., Gallego, V., Pérez, L., Butts, I., Tomkiewicz, J., & Asturiano, J. (2013). Evaluation of Methods to Determine Sperm Density for the European eel,Anguilla anguilla. Reproduction in Domestic Animals, 48(6), 936-944. doi:10.1111/rda.12189Støttrup, J. G., Jacobsen, C., Tomkiewicz, J., & Jarlbaek, H. (2012). Modification of essential fatty acid composition in broodstock of cultured European eelAnguilla anguillaL. Aquaculture Nutrition, 19(2), 172-185. doi:10.1111/j.1365-2095.2012.00967.xStøttrup, J. G., Tomkiewicz, J., Jacobsen, C., Butts, I. A. E., Holst, L. K., Krüger-Johnsen, M., … Kaushik, S. (2015). Development of a broodstock diet to improve developmental competence of embryos in European eel,Anguilla anguilla. Aquaculture Nutrition, 22(4), 725-737. doi:10.1111/anu.12299Dayal, J. S., Ahamad Ali, S., Thirunavukkarasu, A. R., Kailasam, M., & Subburaj, R. (2003). Nutrient an

    Real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion

    Get PDF
    Membrane fusion is the core process in membrane trafficking and is essential for cellular transport of proteins and other biomacromolecules. During protein-mediated membrane fusion, membrane proteins are often excluded from the membrane-membrane contact, indicating that local structural transformations in lipid domains play a major role. However, the rearrangements of lipid domains during fusion have not been thoroughly examined. Here using a newly developed Fluorescence Surface Forces Apparatus (FL-SFA), migration of liquid-disordered clusters and depletion of liquid-ordered domains at the membrane-membrane contact are imaged in real time during hemifusion of model lipid membranes, together with simultaneous force-distance and lipid membrane thickness measurements. The load and contact time-dependent hemifusion results show that the domain rearrangements decrease the energy barrier to fusion, illustrating the significance of dynamic domain transformations in membrane fusion processes. Importantly, the FL-SFA can unambiguously correlate interaction forces and in situ imaging in many dynamic interfacial systems.open0

    Changes in zooplankton community, and seston and zooplankton fatty acid profiles at the freshwater/saltwater interface of the Chowan River, North Carolina

    Get PDF
    The variability in zooplankton fatty acid composition may be an indicator of larval fish habitat quality as fatty acids are linked to fish larval growth and survival. We sampled an anadromous fish nursery, the Chowan River, during spring of 2013 in order to determine how the seston fatty acid composition varied in comparison with the zooplankton community composition and fatty acid composition during the period of anadromous larval fish residency. The seston fatty acid profiles showed no distinct pattern in relation to sampling time or location. The mesozooplankton community composition varied spatially and the fatty acid profiles were typical of freshwater species in April. The Chowan River experienced a saltwater intrusion event during May, which resulted in brackish water species dominating the zooplankton community and the fatty acid profile showed an increase in polyunsaturated fatty acids (PUFA), in particular eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). The saltwater intrusion event was followed by an influx of freshwater due to high precipitation levels in June. The zooplankton community composition once again became dominated by freshwater species and the fatty acid profiles shifted to reflect this change; however, EPA levels remained high, particularly in the lower river. We found correlations between the seston, microzooplankton and mesozooplankton fatty acid compositions. Salinity was the main factor correlated to the observed pattern in species composition, and fatty acid changes in the mesozooplankton. These data suggest that anadromous fish nursery habitat likely experiences considerable spatial variability in fatty acid profiles of zooplankton prey and that are correlated to seston community composition and hydrodynamic changes. Our results also suggest that sufficient prey density as well as a diverse fatty acid composition is present in the Chowan River to support larval fish production

    Flexibility of a Eukaryotic Lipidome – Insights from Yeast Lipidomics

    Get PDF
    Mass spectrometry-based shotgun lipidomics has enabled the quantitative and comprehensive assessment of cellular lipid compositions. The yeast Saccharomyces cerevisiae has proven to be a particularly valuable experimental system for studying lipid-related cellular processes. Here, by applying our shotgun lipidomics platform, we investigated the influence of a variety of commonly used growth conditions on the yeast lipidome, including glycerophospholipids, triglycerides, ergosterol as well as complex sphingolipids. This extensive dataset allowed for a quantitative description of the intrinsic flexibility of a eukaryotic lipidome, thereby providing new insights into the adjustments of lipid biosynthetic pathways. In addition, we established a baseline for future lipidomic experiments in yeast. Finally, flexibility of lipidomic features is proposed as a new parameter for the description of the physiological state of an organism

    RETRACTED ARTICLE: Age-dependent Increase in Desmosterol Restores DRM Formation and Membrane-related Functions in Cholesterol-free DHCR24−/− Mice

    Get PDF
    Cholesterol is a prominent modulator of the integrity and functional activity of physiological membranes and the most abundant sterol in the mammalian brain. DHCR24-knock-out mice lack cholesterol and accumulate desmosterol with age. Here we demonstrate that brain cholesterol deficiency in 3-week-old DHCR24−/− mice was associated with altered membrane composition including disrupted detergent-resistant membrane domain (DRM) structure. Furthermore, membrane-related functions differed extensively in the brains of these mice, resulting in lower plasmin activity, decreased β-secretase activity and diminished Aβ generation. Age-dependent accumulation and integration of desmosterol in brain membranes of 16-week-old DHCR24−/− mice led to the formation of desmosterol-containing DRMs and rescued the observed membrane-related functional deficits. Our data provide evidence that an alternate sterol, desmosterol, can facilitate processes that are normally cholesterol-dependent including formation of DRMs from mouse brain extracts, membrane receptor ligand binding and activation, and regulation of membrane protein proteolytic activity. These data indicate that desmosterol can replace cholesterol in membrane-related functions in the DHCR24−/− mouse

    Cholesterol Induces Specific Spatial and Orientational Order in Cholesterol/Phospholipid Membranes

    Get PDF
    In lipid bilayers, cholesterol facilitates the formation of the liquid-ordered phase and enables the formation of laterally ordered structures such as lipid rafts. While these domains have an important role in a variety of cellular processes, the precise atomic-level mechanisms responsible for cholesterol's specific ordering and packing capability have remained unresolved

    Cholesterol Induces Specific Spatial and Orientational Order in Cholesterol/Phospholipid Membranes

    Get PDF
    In lipid bilayers, cholesterol facilitates the formation of the liquid-ordered phase and enables the formation of laterally ordered structures such as lipid rafts. While these domains have an important role in a variety of cellular processes, the precise atomic-level mechanisms responsible for cholesterol's specific ordering and packing capability have remained unresolved

    Evolutionary effects of alternative artificial propagation programs: implications for viability of endangered anadromous salmonids

    Get PDF
    Most hatchery programs for anadromous salmonids have been initiated to increase the numbers of fish for harvest, to mitigate for habitat losses, or to increase abundance in populations at low abundance. However, the manner in which these programs are implemented can have significant impacts on the evolutionary trajectory and long-term viability of populations. In this paper, we review the potential benefits and risks of hatchery programs relative to the conservation of species listed under the US Endangered Species Act. To illustrate, we present the range of potential effects within a population as well as among populations of Chinook salmon (Oncorhynchus tshawytscha) where changes to major hatchery programs are being considered. We apply evolutionary considerations emerging from these examples to suggest broader principles for hatchery uses that are consistent with conservation goals. We conclude that because of the evolutionary risks posed by artificial propagation programs, they should not be viewed as a substitute for addressing other limiting factors that prevent achieving viability. At the population level, artificial propagation programs that are implemented as a short-term approach to avoid imminent extinction are more likely to achieve long-term population viability than approaches that rely on long-term supplementation. In addition, artificial propagation programs can have out-of-population impacts that should be considered in conservation planning
    corecore