atlantic halibut
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2022 ◽  
Vol 22 ◽  
pp. 100958
Author(s):  
Pablo Gallardo ◽  
Guilherme Wolff Bueno ◽  
Cristian Araneda ◽  
Tillmann Benfey

Nutrients ◽  
2021 ◽  
Vol 14 (1) ◽  
pp. 195
Author(s):  
Matthew Sprague ◽  
Tsz Chong Chau ◽  
David I. Givens

Iodine is an important nutrient for human health and development, with seafood widely acknowledged as a rich source. Demand from the increasing global population has resulted in the availability of a wider range of wild and farmed seafood. Increased aquaculture production, however, has resulted in changes to feed ingredients that affect the nutritional quality of the final product. The present study assessed the iodine contents of wild and farmed seafood available to UK consumers and evaluated its contribution to current dietary iodine intake. Ninety-five seafood types, encompassing marine and freshwater fish and shellfish, of wild and farmed origins, were purchased from UK retailers and analysed. Iodine contents ranged from 427.4 ± 316.1 to 3.0 ± 1.6 µg·100 g−1 flesh wet weight (mean ± SD) in haddock (Melanogrammus aeglefinus) and common carp (Cyprinus carpio), respectively, being in the order shellfish > marine fish > freshwater fish, with crustaceans, whitefish (Gadiformes) and bivalves contributing the greatest levels. Overall, wild fish tended to exhibit higher iodine concentrations than farmed fish, with the exception of non-fed aquaculture species (bivalves). However, no significant differences were observed between wild and farmed Atlantic salmon (Salmo salar), rainbow trout (Oncorhynchus mykiss), and turbot (Psetta maxima). In contrast, farmed European seabass (Dicentrarchus labrax) and seabream (Sparus aurata) presented lower, and Atlantic halibut (Hippoglossus hippoglossus) higher, iodine levels than their wild counterparts, most likely due to the type and inclusion level of feed ingredients used. By following UK dietary guidelines for fish consumption, a portion of the highest oily (Atlantic mackerel, Scomber scombrus) and lean (haddock) fish species would provide two-thirds of the weekly recommended iodine intake (980 µg). In contrast, actual iodine intake from seafood consumption is estimated at only 9.4–18.0% of the UK reference nutrient intake (140 µg·day−1) across different age groups and genders, with females obtaining less than their male equivalents.


2021 ◽  
pp. 47-111
Author(s):  
Jason S. Link ◽  
Anthony R. Marshak

This chapter describes the New England region and the major issues facing this marine fisheries ecosystem, and presents some summary statistics related to the 90 indicators of ecosystem-based fisheries management (EBFM) criteria. New England contains the second-lowest number of managed taxa among U.S. marine ecosystems, including historically important groundfish species such as Atlantic cod, haddock, Atlantic halibut, commercially valuable Atlantic sea scallop and American lobster, and federally protected Atlantic salmon. The New England social-ecological system is an environment that is responding to the consequences of overfishing, habitat loss, coastal development, and nutrient loading. Overall, EBFM progress has been made at the regional and subregional levels in implementing ecosystem-level planning, advancing knowledge of ecosystem principles, and examining system trade-offs. While much information has been obtained and applied regarding ecosystem-level calculations, syntheses, and models, only partial progress has been observed in using these system-wide emergent properties in management actions. Despite many of these large-scale efforts toward greater scientific understanding of the New England ecosystem, challenges remain toward effectively implementing formalized EBFM management actions and enacting ecosystem-level control rules. Namely, this region currently lacks a completed fishery ecosystem plan (FEP), and only partial progress has occurred toward considering system catch limits for this region. This ecosystem is excelling in the socioeconomic status of its LMRs, and is relatively productive, as related to the determinants of successful LMR management.


Neuropeptides ◽  
2021 ◽  
pp. 102202
Author(s):  
Ana S. Gomes ◽  
Endre Lygre ◽  
Torstein Harboe ◽  
Fabian Zimmermann ◽  
Ann-Elise O. Jordal ◽  
...  

Author(s):  
Nancy L. Shackell ◽  
Jonathan A. D. Fisher ◽  
Cornelia E. den Heyer ◽  
Daniel R. Hennen ◽  
Andrew C. Seitz ◽  
...  

2021 ◽  
Vol 770 ◽  
pp. 145349
Author(s):  
Prescilla Perrichon ◽  
Carey E. Donald ◽  
Elin Sørhus ◽  
Torstein Harboe ◽  
Sonnich Meier

Aquaculture ◽  
2021 ◽  
pp. 736733
Author(s):  
Diana B. Reis ◽  
José A. Pérez ◽  
Kristin Hamre ◽  
Nieves G. Acosta ◽  
Birgitta Norberg ◽  
...  

2020 ◽  
Author(s):  
Rolf Brudvik Edvardsen ◽  
Ola Wallerman ◽  
Tomasz Furmanek ◽  
Lene Kleppe ◽  
Patric Jern ◽  
...  

Atlantic Halibut (Hippoglossus hippoglossus) has a X/Y genetic sex determination system, but the sex determining factor is not known. We produced a high-quality genome assembly and identified parts of chromosome 13 as the Y chromosome due to sequence divergence between sexes and segregation of sex genotypes in pedigrees. Linkage analysis revealed that all chromosomes exhibit heterochiasmy, i.e. male- and female restricted meiotic recombination intervals (MRR/FRR). We show that FRR/MRR intervals differ in nucleotide diversity and repeat class content and that this is true also for other Pleuronectidae species. We further show that remnants of a Gypsy-like transposable element insertion on chr13 promotes early male specific expression of gonadal somatic cell derived factor (gsdf). Less than 4 MYA, this male-determining element evolved on an autosomal FRR segment featuring pre-existing male meiotic recombination barriers, thereby creating a Y chromosome. We propose that heterochiasmy may facilitate the evolution of genetic sex determination systems.


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