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Publication
Featured researches published by A. Belmonte.
General and Comparative Endocrinology | 2012
Hanna Rosenfeld; Constantinos C. Mylonas; C.R. Bridges; Gilad Heinisch; A. Corriero; R. Vassallo-Aguis; A. Medina; A. Belmonte; A. García; F. de la Gándara; C. Fauvel; G. De Metrio; I. Meiri-Ashkenazi; H. Gordin; Yonathan Zohar
A controlled-release implant loaded with GnRH agonist (GnRHa) was used to induce spawning in Atlantic bluefin tuna (Thunnus thynnus) during two consecutive reproductive seasons. The fish were implanted underwater and sampled between days 2 and 8 after treatment. At the time of GnRHa treatment, females were in full vitellogenesis and males in spermiation. There was a rapid burst of pituitary luteinizing hormone (LH) release at day 2 after treatment in GnRHa-treated fish, and circulating LH remained elevated up to day 8 after treatment. In contrast, control fish had significantly lower levels in the plasma, but higher LH content in the pituitary, as observed in many other cultured fishes that fail to undergo oocyte maturation, ovulation and spawning unless induced by an exogenous GnRHa. Plasma testosterone (T) and 17β-estradiol (E(2)) were elevated in response to the GnRHa treatment in females, while 11-ketotestosterone (11-KT) but not T was elevated in males. Even though oocyte maturation and ovulation did occur in GnRHa-induced fish, no significant elevations in 17,20β-dihydroxy-4-pregnen-3-one (17,20β-P) or 17,20β,21-trihydroxy-4-pregnen-3-one (20β-S), in either the free, conjugated or 5β-reduced,3α-hydroxylated forms was observed in fish sampled within 6 days after treatment. Interestingly, a significant peak in plasma free 17,20β-P levels occurred in both males and females at day 8 after treatment. Histological sections of the ovaries in these females contained oocytes at the migrating germinal vesicle stage, suggesting the role of this hormone as a maturation-inducing steroid in Atlantic bluefin tuna. In conclusion, the GnRHa implants activated effectively the reproductive endocrine axis in captive Atlantic bluefin tuna broodstocks, through stimulation of sustained elevations in plasma LH, which in turn evoked the synthesis and secretion of the relevant sex steroids leading to gamete maturation and release.
Reviews in Fisheries Science | 2013
José L. Cort; Simeon Deguara; Txema Galaz; Begonya Mèlich; Iñaki Artetxe; Igor Arregi; John D. Neilson; Irene Andrushchenko; Alex Hanke; Miguel N. Santos; Vicente D. Estruch; Molly Lutcavage; Jessica M. Knapp; Guillermo Compeán-Jiménez; Rafael Solana-Sansores; A. Belmonte; David Martínez; Corrado Piccinetti; Ai Kimoto; Piero Addis; Marta Velasco; José M. de la Serna; Dolores Godoy; Tevfik Ceyhan; I. K. Oray; Saadet Karakulak; Leif Nøttestad; Antonio José Fernández López; Oriol Ribalta; Noureddine Abid
A meta-analysis of the straight fork lengths (herewith abbreviated as L) of 2,458,028 Atlantic bluefin tuna, Thunnus thynnus (L.), taken from 224 scientific publications and unpublished L data from scientific organizations and fishing companies spanning most of the known Atlantic and Mediterranean Atlantic bluefin tuna fisheries dating from 1605 to 2011, give L values ranging from L min = 20 cm and L max = 330 cm. The results indicate that the parameter L ∞ = 318.85 cm of the growth equation used by ICCATs Standing Committee on Research and Statistics Atlantic bluefin tuna assessment group for the eastern stock (Lt = 318.85 [1 – e−0.093 (t + 0.97)]) lies within the confidence limits of the maximum Ls presented in the study: L max = 319.93 ± 11.3 cm, confirming that this equation perfectly fits the biology of the growth of this species. These conclusions are also valid for the equation for the western stock (Lt = 314.90 [1 – e−0.089 (t +1.13)]). The ICCAT Atlantic bluefin tuna database contains numerous records of Atlantic bluefin tuna L outside the biological feasibility, and solutions are provided to recognize and remove these outliers based on the application of fixed values of Fultons condition factor (K) between 1.4 and 2.6 and appropriate L-W relationships to correct this situation in the future.
Aquaculture | 2007
A. Corriero; Antonio Medina; Constantinos C. Mylonas; Francisco J. Abascal; M. Deflorio; Lourdes Aragón; C.R. Bridges; N. Santamaria; Gilad Heinisch; R. Vassallo-Agius; A. Belmonte; C. Fauvel; A. García; H. Gordin; G. De Metrio
Marine Ecology Progress Series | 2007
Antonio Medina; Francisco J. Abascal; Lourdes Aragón; Gabriel Mourente; Guillermo Aranda; Txema Galaz; A. Belmonte; J. Miguel de la Serna; Salvador García
Aquaculture | 2011
Guillermo Aranda; Lourdes Aragón; A. Corriero; Constantinos C. Mylonas; Fernando de la Gándara; A. Belmonte; Antonio Medina
ICCAT Collective Volume of Scientific Papers | 2012
Vicente Puig Pons; Víctor Espinosa Roselló; Ester Soliveres González; Aurelio Ortega; A. Belmonte; Fernando de la Gándara García
Indian journal of science and technology | 2011
E. Yanowski; Constantinos C. Mylonas; A. Corriero; C.R. Bridges; R. Vassallo-Aguis; F. De La Gandara; A. Belmonte; I. Meiri-Ashkenazi; H. Gordin; Hanna Rosenfeld
Indian journal of science and technology | 2011
N. Berkovich; A. Corriero; N. Santamaria; Constantinos C. Mylonas; C.R. Bridges; R. Vassallo-Aguis; F. De La Gandara; A. Belmonte; K. Mislov; I. Katavic; A. Elizur; I. Meiri-Ashkenazi; H. Gordin; Hanna Rosenfeld
Archive | 2005
A. García-Gómez; M.V. Díaz; F. de-la-Gándara; J.M. de-la-Serna; A. Belmonte; E. Ayora; H. Gordin; C. Fauvel; A. Medina; C.R. Bridges; R. Vassallo-Agius; Constantinos C. Mylonas; G. De Metrio
Instrumentation viewpoint | 2011
Vicente Puig; V. Espinosa; Ester Soliveres; Aurelio Ortega; A. Belmonte; Fernando de la Gándara