Nutritional Composition Differences of Alaska Pollock (Gadus Chalcogrammus) During and Between Bering Sea a and B Seasons Clara A

Total Page:16

File Type:pdf, Size:1020Kb

Nutritional Composition Differences of Alaska Pollock (Gadus Chalcogrammus) During and Between Bering Sea a and B Seasons Clara A NUTRITIONAL COMPOSITION DIFFERENCES OF ALASKA POLLOCK (GADUS CHALCOGRAMMUS) DURING AND BETWEEN BERING SEA A AND B SEASONS CLARA A. HINTERMEISTER, CHRISTINA A. MIRELES DEWITT, QUENTIN FONG COASTAL OREGON MARINE EXPERIMENT STATION OSU SEAFOOD LAB ASTORIA, OR BACKGROUND • Schooling whitefish native to North Pacific • One of the largest single- species fisheries in the world • Majority caught in the Bering Sea • Season A: winter-spring • Season B: summer-fall BACKGROUND • Economically valuable: • 45% of production volume and 33% of total value of Alaska fisheries in 2014 • 67% of total Alaska groundfish catch in 2015 • Many products produced from Alaska Pollock: • Surimi and surimi seafood • Fillets • Fish Sticks • Mentaiko and Tarako • Shirako • Fish meal OBJECTIVES AND IMPORTANCE • To determine if seasonality and catch date affect nutritional composition • To develop nutrition profile(s) for Alaska Pollock fillets, milt and roe • To provide valuable information to processors about possible composition changes • To aid in the development of value-added Alaska Pollock products SAMPLE COLLECTION AMERICAN SEAFOODS, 2015 A Season B Season Fillet, Roe, Milt – Fillet, Roe* – n=10/date/type n=10/date/type • February 3 • July 15 • February 17 • August 15 • March 3 • March 16 *Roe only on 7/15 • March 31 Ntotal = 150 Ntotal = 30 ANALYSES PROXIMATE: • FAT • PROTEIN • MOISTURE • ASH FAT-SOLUBLE VITAMINS (A, D, E) FATTY ACIDS AMINO ACIDS MINERALS PROXIMATE ANALYSIS Fat Protein Acid hydrolysis Kjeldahl nitrogen Mojonnier determination Moisture Ash Drying oven Muffle furnace 16 h at 103°C 12- 48 h at 525°C VITAMIN METHOD DEVELOPMENT • Based off Zonta (1982) • Two 25 cm C18 columns • 44°C • Mobile phase: • A - 80% Acetonitrile / 20% Methanol • B - Water • Flow rate:1.5 ml/min • 40 minute gradient program VITAMIN METHOD DEVELOPMENT Vitamin E Standard Curve Vitamin D2 Standard Curve 400000 100000 y = 281250x - 1317.5 y = 1E+06x - 1019.8 300000 80000 R² = 0.9961 R² = 0.9998 60000 200000 Area 40000 Axis Title 100000 20000 0 0 0 0.5 1 1.5 0 0.02 0.04 0.06 0.08 ug Alpha-Tocopherol ug Ergocalciferol E A D2 D3 Vitamin A Standard Curve Vitamin D3 Standard Curve 800000 120000 y = 6E+06x - 898.66 100000 y = 2E+06x - 187.13 600000 R² = 0.9989 80000 R² = 0.9998 400000 60000 Area Area 40000 200000 20000 0 0 0 0.02 0.04 0.06 0.08 0.1 0.12 0 0.02 0.04 0.06 0.08 ug Retinol ug Cholecalciferol VITAMIN METHOD DEVELOPMENT • Saponification • 50% KOH • 30 minutes at 70°C • Extraction • Hexane • Evaporation • Under nitrogen • Sample resuspended in 50% ethanol/50% methanol VITAMIN METHOD DEVELOPMENT Fillet A D2 D3 E Milt E A D2 D3 Roe E A D2 D3 RESULTS – FILLET PROXIMATE ANALYSIS Sample Date % Fat % Protein % Moisture % Ash 2/3/15 0.44 ± 0.20 14.51 ± 0.83 83.07 ± 0.37 1.31 ± 0.02a 2/17/15 0.40 ± 0.09 14.87 ± 0.86 83.12 ± 0.59 1.30 ± 0.08ab 3/3/15 0.46 ± 0.08 15.13 ± 0.57 83.07 ± 0.78 1.35 ± 0.04ab 3/16/15 0.37 ± 0.14 15.14 ± 0.88 83.31 ± 0.53 1.36 ± 0.05b 3/31/15 0.39 ± 0.08 15.23 ± 0.89 83.77 ± 1.10 1.29 ± 0.06ab Season A Average 0.41 ± 0.13 14.98 ± 0.82 83.27 ± 0.37 1.32 ± 0.02 7/15/15 0.57 ± 0.10x 16.18 ± 0.71x 82.61 ± 0.68 1.45 ± 0.07x 8/15/15 0.44 ± 0.08y 15.35 ± 0.68y 83.02 ± 0.53 1.36 ± 0.08y Season B Average 0.50 ± 0.10* 15.77 ± 0.80* 83.02 ± 0.53* 1.40 ± 0.07* * Denotes Season B averages significantly different from Season A averages (p<0.05) ab Denotes significant differences within Season A (p<0.05) xy Denotes significant differences within Season B (p<0.05) RESULTS – ROE PROXIMATE ANALYSIS Sample Date % Fat % Protein % Moisture % Ash 2/3/15 1.72 ± 0.16 23.99 ± 3.00 71.45 ± 2.74 1.61 ± 0.16 2/17/15 1.78 ± 0.28 23.66 ± 2.36 71.13 ± 2.51 1.49 ± 0.11 3/3/15 1.64 ± 0.34 22.92 ± 2.14 71.56 ± 2.42 1.63 ± 0.30 3/16/15 1.62 ± 0.23 23.36 ± 1.16 71.70 ± 1.54 1.64 ± 0.18 3/31/15 1.64 ± 0.17 22.53 ± 2.01 72.41 ± 5.83 1.63 ± 0.21 Season A Average 1.68 ± 0.24 23.17 ± 1.87 71.65 ± 2.28 1.60 ± 0.20 Season B Average 2.87 ± 0.20* 23.60 ± 2.11 70.22 ± 5.80* 1.63 ± 0.14 * Denotes Season B averages significantly different from Season A averages (p<0.05) RESULTS – MILT PROXIMATE ANALYSIS Sample Date % Fat % Protein % Moisture % Ash 2/3/15 1.93 ± 0.17ab 12.77 ± 0.17 84.60 ± 0.07ab 1.71 ± 0.08bcd 2/17/15 2.13 ± 0.53b 12.22 ± 0.53 85.30 ± 0.07a 1.61 ± 0.07ad 3/3/15 1.99 ± 0.20a 12.44 ± 0.20 84.92 ± 0.04ab 1.56 ± 0.07a 3/16/15 1.72 ± 0.18a 12.37 ± 0.18 84.91 ± 0.14ab 1.64 ± 0.08abcd 3/31/15 1.75 ± 0.17ab 13.02 ± 0.17 84.10 ± 0.11b 1.75 ± 0.06bc Season A Average 1.91 ± 0.32 12.57 ± 0.77 84.76 ± 0.85 1.65 ± 0.11 abcd Denotes significant differences within Season A (p<0.05) RESULTS - FAT Changes in Fat Content During and Between Catch Seasons for Fillets, Milt and Roe 3 2.5 2 Fillets 1.5 Roe % Fat Milt 1 Season A Season B 0.5 0 1-Feb 1-Mar 1-Apr 1-May 1-Jun 1-Jul 1-Aug Catch Date RESULTS – FILLET VITAMINS Sample Date A (µg/85 g) D3 (µg/85 g) E (mg/85 g) 2/3/15 2.78 ± 0.68a 0.76 ± 0.36 0.25 ± 0.21 2/17/15 3.80 ± 0.85b 0.74 ± 0.31 0.23 ± 0.17 3/3/15 2.29 ± 0.64b 0.57 ± 0.28 0.35 ± 0.19 3/16/15 2.89 ± 0.32ab 0.77 ± 0.25 0.25 ± 0.21 3/31/15 3.63 ± 0.97ab 1.25 ± 0.88 0.47 ± 0.17 Season A Average 3.38 ± 0.83 0.87 ± 0.50 0.31 ± 0.20 7/15/15 3.79 ± 0.67 1.32 ± 0.41 0.20 ± 0.11x 8/15/15 4.52 ± 1.20 1.33 ± 0.59 0.42 ± 0.22y Season B Average 4.14 ± 1.00* 1.33 ± 0.49* 0.31 ± 0.20 * Denotes Season B averages significantly different from Season A averages (p<0.05) ab Denotes within Season A xy Denotes changes within Season B RESULTS – ROE VITAMINS Sample Date A (µg/15 g) D3 (µg/15 g) E (mg/15 g) 2/3/15 7.61 ± 4.61ab 1.10 ± 0.45ac 0.76 ± 0.37 2/17/15 6.45 ± 3.19ab 1.38 ± 0.82c 0.78 ± 0.28 3/3/15 15.16 ± 9.74a 0.74 ± 0.69a 1.03 ± 0.45 3/16/15 6.28 ± 3.45b 0.72 ± 0.27ac 1.01 ± 0.44 3/31/15 11.99 ± 7.93ab 0.57 ± 0.27b 0.93 ± 0.55 Season A Average 9.38 ± 6.92 0.90 ± 0.60 0.91 ± 0.43 Season B Average 10.87 ± 4.70 0.32 ± 0.15* 0.90 ± 0.35 * Denotes Season B averages significantly different from Season A averages (p<0.05) abc Denotes significant differences within Season A (p<0.05) xy Denotes significant differences within Season B (p<0.05) RESULTS – MILT VITAMINS Sample Date A (µg/15 g) D3 (µg/15 g) E (mg/15 g) 2/3/15 2.94 ± 1.64 0.13 ± 0.06 0.25 ± 0.12 2/17/15 3.70 ± 1.41 0.19 ± 0.19 0.25 ± 0.12 3/3/15 4.86 ± 1.99 0.15 ± 0.19 0.29 ± 0.21 3/16/15 3.48 ± 1.13 0.12 ± 0.15 0.19 ± 0.13 3/31/15 3.51 ± 1.80 0.21 ± 0.18 0.28 ± 0.16 Season A Average 3.70 ± 1.70 0.16 ± 0.16 0.25 ± 0.15 NUTRITION LABELING- THINGS TO KNOW • Protein % daily values not accurate without amino acid profile • Amounts of saturated and trans fats will be determined with fatty acid profile • Vitamin daily values based on recommended daily intake amounts • Vitamin A – 900 µg • Vitamin D – 20 µg • Vitamin E – 15 mg Season A Season B NUTRITION LABELS- FILLETS • Differences: • Calories • Vitamin D • Things to note: • Fat is 0 g • Vitamin A is 0% DV • Protein %DV may not be accurate since amino acid profile not completed NUTRITION LABELS- ROE • Differences: • Calories • Vitamin D • Vitamin A • Things to note: • Fat is 0 g • Protein %DV may not be accurate since amino acid profile not completed Season A Season B NUTRITION LABEL - MILT • Things to note: • Fat is 0 g • Vitamin D is 0% DV • Vitamin A is 0% DV • Protein %DV may not be accurate since amino acid profile not completed COMPARING FILLETS, MILT AND ROE- VITAMINS PER 100 g Type Season Vitamin A (µg/100g) Vitamin D (µg/100g) Vitamin E (mg/100g) Fillet A 3.97 5.77 5.09 B 4.87 8.84 7.80 Roe A 62.54 5.97 6.04 B 72.46 2.14 5.99 Milt A 24.68 1.07 1.68 % DV OF VITAMINS PER 100 g SAMPLE ON A WET AND DRY BASIS Type Season Vitamin A (% DV) Vitamin D (% DV) Vitamin E (% DV) Wet Dry Wet Dry Wet Dry Fillet A 0.44 2.64 5.09 30.45 2.41 14.39 B 0.54 3.15 7.80 45.40 2.43 14.14 Roe A 6.95 24.51 29.84 105.26 40.30 142.14 B 8.05 27.04 10.72 36.00 39.92 134.04 Milt A 2.74 18.00 5.36 35.18 11.22 73.59 Reference Daily Intake (RDI) values for adults and children ≥ 4 years: Vitamin A – 900 µg Vitamin D – 20 µg Vitamin E – 15 mg PROXIMATE ANALYSIS – DRY BASIS Type Season % Fat % Protein % Ash Fillet A 2.42 ± 0.79 88.06 ± 11.53 7.91 ± 0.39 B 2.930 ± 0.62 91.78 ± 4.10 8.15 ± 0.37 Roe A 5.94 ± 0.85 81.98 ± 6.77 5.70 ± 1.00 B 9.69 ± 0.90 79.34 ± 4.62 5.52 ± 0.81 Milt A 12.54 ± 2.17 82.52 ± 3.71 10.84 ± 0.47 THOUGHTS AND CONCLUSIONS • Roe and milt had higher fat content than fillets (2% compared to <0.5%) • Roe was highest in protein (23%) and all vitamins and lowest in moisture (71%).
Recommended publications
  • Snakeheadsnepal Pakistan − (Pisces,India Channidae) PACIFIC OCEAN a Biologicalmyanmar Synopsis Vietnam
    Mongolia North Korea Afghan- China South Japan istan Korea Iran SnakeheadsNepal Pakistan − (Pisces,India Channidae) PACIFIC OCEAN A BiologicalMyanmar Synopsis Vietnam and Risk Assessment Philippines Thailand Malaysia INDIAN OCEAN Indonesia Indonesia U.S. Department of the Interior U.S. Geological Survey Circular 1251 SNAKEHEADS (Pisces, Channidae)— A Biological Synopsis and Risk Assessment By Walter R. Courtenay, Jr., and James D. Williams U.S. Geological Survey Circular 1251 U.S. DEPARTMENT OF THE INTERIOR GALE A. NORTON, Secretary U.S. GEOLOGICAL SURVEY CHARLES G. GROAT, Director Use of trade, product, or firm names in this publication is for descriptive purposes only and does not imply endorsement by the U.S. Geological Survey. Copyrighted material reprinted with permission. 2004 For additional information write to: Walter R. Courtenay, Jr. Florida Integrated Science Center U.S. Geological Survey 7920 N.W. 71st Street Gainesville, Florida 32653 For additional copies please contact: U.S. Geological Survey Branch of Information Services Box 25286 Denver, Colorado 80225-0286 Telephone: 1-888-ASK-USGS World Wide Web: http://www.usgs.gov Library of Congress Cataloging-in-Publication Data Walter R. Courtenay, Jr., and James D. Williams Snakeheads (Pisces, Channidae)—A Biological Synopsis and Risk Assessment / by Walter R. Courtenay, Jr., and James D. Williams p. cm. — (U.S. Geological Survey circular ; 1251) Includes bibliographical references. ISBN.0-607-93720 (alk. paper) 1. Snakeheads — Pisces, Channidae— Invasive Species 2. Biological Synopsis and Risk Assessment. Title. II. Series. QL653.N8D64 2004 597.8’09768’89—dc22 CONTENTS Abstract . 1 Introduction . 2 Literature Review and Background Information . 4 Taxonomy and Synonymy .
    [Show full text]
  • Management of Shark Fin Trade to and from Australia
    MANAGEMENT Scalloped hammerhead sharks OF SHARK FIN TRADE TO AND FROM AUSTRALIA In preparing this report the author has made all reasonable efforts to ensure the information it contains is based on evidence. The TABLE OF CONTENTS views expressed in this report are those of the author based on that evidence. The author does not guarantee that there is not further evidence relevant to the matters covered 1. Executive Summary 2 by this report and therefore urges those with an interest in these matters to conduct their own due 2. Introduction 5 diligence and to draw their own conclusions. 3. Shark Fin Trade 7 Trends in shark fin trade 8 Australian shark fin trade 13 4. Shark Fishery Management 17 5. Fins Naturally Attached 23 6. Traceability 29 Principle 1: Unique Identification 31 Principle 2: Data Capture and Management 31 Principle 3: Data Communication 33 7. Managing International Trade 34 8. Conclusion 36 Annex A – Protected Species as of October 2020 38 Annex B – Country Specific HS Codes for Shark Fin 40 Annex C – Fisheries Specific Shark Management Measures 45 EXECUTIVE SUMMARY Healthy shark populations are an indicator of the health of the marine environment. Sharks play This report looks at the current trends in the global a key role in marine and estuarine environments, and people around the world rely on healthy shark fin trade and actions that Australia can take marine ecosystems for their livelihoods. It has been predicted that by 2033, shark based eco- to drive improvement in the shark fin industry, tourism will be worth more than 785 million USD.
    [Show full text]
  • Sperm Cryopreservation
    animals Article Effects of Cryoprotective Medium Composition, Dilution Ratio, and Freezing Rates on Spotted Halibut (Verasper variegatus) Sperm Cryopreservation Irfan Zidni 1 , Yun Ho Lee 1, Jung Yeol Park 1, Hyo Bin Lee 1, Jun Wook Hur 2 and Han Kyu Lim 1,* 1 Department of Marine and Fisheries Resources, Mokpo National University, Mokpo 58554, Korea; [email protected] (I.Z.); [email protected] (Y.H.L.); [email protected] (J.Y.P.); [email protected] (H.B.L.) 2 Faculty of Marine Applied Biosciences, Kunsan National University, 558 Daehak-ro, Gunsan, Jeonbuk 54150, Korea; [email protected] * Correspondence: [email protected]; Tel.: +82-61-450-2395; Fax: +82-61-452-8875 Received: 12 October 2020; Accepted: 16 November 2020; Published: 19 November 2020 Simple Summary: The spotted halibut, Verasper variegatus, is a popular fish species occurring naturally in the East China Sea and coastal areas of Korea and Japan. However, when reared in captivity, male and female spotted halibut do not usually mature synchronously. Maintaining production of this commercial fish in hatcheries through sperm cryopreservation is important. This study investigated the effect of several factors for successful cryopreservation of fish sperm including cryoprotective agents (CPAs), diluents, dilution ratios (Milt: CPA + diluents), and freezing rates. The observed factors significantly affected movable sperm ratio (MSR), sperm activity index (SAI), survival rate, and DNA damage after cryopreservation. In the present study, the mixture of 15% dimethyl sulfoxide (DMSO) + 300 mM sucrose with a dilution ratio lower than 1:2 and a freezing rate slower than 5 C/min provided the best treatment and reduced DNA damage.
    [Show full text]
  • Channel Catfish Review Life-History, Distribution, Invasion Dynamics and Current Management Strategies in the Pacific Northwest
    Channel Catfish Review Life-history, distribution, invasion dynamics and current management strategies in the Pacific Northwest Thomas K Pool University of Washington Figure 1 Illustration of a channel catfish by Ted Walke (http://www.fish.state.pa.us/pafish/chancatm.jpg) Figure 2 Thomas L. Wellborn SRAC Publication No. 180 http://www.tpwd.state.tx.us/huntwild/wild/species/ccf/) Figure 3 Channel catfish: Note the barbels Figure 4 Channel catfish: Characteristic deeply forked located near the mouth© George tail © George Burgess (http://www.flmnh.ufl.edu) Burgess(http://www.flmnh.ufl.edu) All information in this report was compiled in November, 2007. Current distribution maps and background information may be outdated at this time. Diagnostic information 1a) Adipose fin a flag-like fleshy lobe, well- separated from caudal fin; tail squared, rounded, Ictalurus punctatus (Rafinesque, 1818) or forked; adults to over 24 inches Kingdom Animalia-- animals 1b) Adipose fin long, low, and 'keel-like', nearly Phylum Chordata-- chordates continuous with caudal fin; tail squared or Subphylum Vertebrata-- vertebrates rounded; adults small, never over 6 inches Superclass Osteichthyes-- bony fishes 2a) Tail deeply-forked, lobes pointed; anal fin Class Actinopterygii-- ray-finned fishes, spiny with 24 to 30 rays; bony ridge connecting skull rayed fishes and origin of dorsal fin; head relatively small Subclass Neopterygii-- neopterygians and narrow; young with small spots, larger Infraclass Teleostei adults blue-black in color without spots channel Superorder Ostariophysi catfish Ictalurus punctatus Order Siluriformes-- catfishes Family Ictaluridae Overview Genus Ictalurus Species Ictalurus punctatus Channel catfish are often grey or silver in color and can be one of the largest catfish species with a maximum size up to 915 mm and Basic identification 13 kg.
    [Show full text]
  • Herring Milt and Herring Milt Protein Hydrolysate Are Equally Effective In
    marine drugs Article Herring Milt and Herring Milt Protein Hydrolysate Are Equally Effective in Improving Insulin Sensitivity and Pancreatic Beta-Cell Function in Diet-Induced Obese- and Insulin-Resistant Mice Yanwen Wang 1,2,* , Sandhya Nair 1,3 and Jacques Gagnon 3,4,* 1 Aquatic and Crop Resource Development Research Center, National Research Council of Canada, Charlottetown, PE C1A 4P3, Canada; [email protected] 2 Department of Biomedical Sciences, University of Prince Edward Island, Charlottetown, PE C1A 4P3, Canada 3 VALORES¯ Research Institute, Shippagan, NB E8S 1J2, Canada 4 Department of Sciences, Shippagan Campus, University of Moncton, Shippagan, NB E8S 1P6, Canada * Correspondence: [email protected] (Y.W.); [email protected] (J.G.) Received: 24 October 2020; Accepted: 8 December 2020; Published: 11 December 2020 Abstract: Although genetic predisposition influences the onset and progression of insulin resistance and diabetes, dietary nutrients are critical. In general, protein is beneficial relative to carbohydrate and fat but dependent on protein source. Our recent study demonstrated that 70% replacement of dietary casein protein with the equivalent quantity of protein derived from herring milt protein hydrolysate (HMPH; herring milt with proteins being enzymatically hydrolyzed) significantly improved insulin resistance and glucose homeostasis in high-fat diet-induced obese mice. As production of protein hydrolysate increases the cost of the product, it is important to determine whether a simply dried and ground herring milt product possesses similar benefits. Therefore, the current study was conducted to investigate the effect of herring milt dry powder (HMDP) on glucose control and the associated metabolic phenotypes and further to compare its efficacy with HMPH.
    [Show full text]
  • Red Drum: Reproductive Biology, Broodstock Management, and Spawning
    SOUTHERN REGIONAL SRAC Publication No. 0320 AQUACULTURE CENTER October 2018 VI PR Red Drum: Reproductive Biology, Broodstock Management, and Spawning Todd Sink1, Robert Vega2, and Jennifer Butler2 The red drum Sciaenops( ocellatus), also known as 1980's regulations proliferated until commercial harvest redfish, is a popular marine sportfish and aquacultured was eliminated throughout the Gulf. Recreational fishing food fish. The red drum is a coastal inshore and nearshore is still permissible but is highly regulated. Demand for species of the western Atlantic ranging from Massachusetts red drum as a food fish commercially remained despite south to the Florida Keys and Bahamas, and throughout the void in supply left by the closure of commercial har- the Gulf of Mexico from Florida to northern Mexico, vest in the Gulf, and as a result culture of red drum has but is largely absent from the Yucatan Peninsula. Recre- become a moving force in marine and inshore aquacul- ational fishermen along the Gulf and lower Atlantic Coasts ture as food fish and for enhancement of wild stocks. have prized the red drum as a challenging, hard-fighting A detailed understanding of the reproductive biology sportfish. Red drum was commercially harvested due to its of red drum and how to successfully manipulate environ- popularity as food fish including dishes such as blackened mental conditions and broodfish physiology is required redfish, redfish Pontchartrain, and redfish on the half shell. for reliable production of eggs and larvae. Significant Production of red drum began in the 1970s to supplement but well-documented technical expertise is required to declining wild stocks, and production as a food fish has secure and maintain healthy red drum broodstock, to since grown into a global aquaculture industry.
    [Show full text]
  • How Does Iceland Manage to Use 85% of a Cod?
    Landing Obligation 2019: What have we learned, what are the next steps? A Science - Policy conference for the closing of H2020 DiscardLess project How does Iceland manage to use 85% of a cod? Jónas R. Viðarsson Matís Ltd. Iceland The Big Picture 71% of the world’s is covered by water Total food production (5.000 million tn) 3.5% Total fish production (178 million tn) Source: FAO food outlook 2018 Jónas R. Viðarsson ©Matís The Big Picture What of this actually becomes human food? Biomass lost as discards at sea 10% on average • EU finfish discards 20-60% prior to LO Utilization in processing of finfish 30-75% • Common to have 40% utilization for finfish Biomass wasted in retail & distribution 7% Biomass wasted at consumer level 28% In the end it is only 21% of the catch that is actually consumed Jónas R. Viðarsson ©Matís Source: (Maria Amparo Pérez Roda et al. 2019 and Love et a.l 2015) Whole fish 116 100,0% Roes / Milt 5 4,3% liver 5 4,3% Viscera 6 5,2% Head 30 25,9% Fraim 18 15,5% Pinbones & cutoffs 2 1,7% Skin 4 3,4% Bellyflap 3 2,6% Fillet 43 37,1% Jónas R. Viðarsson ©Matís …also Skin Viscera Swim bladder Pharmaceuticals Nutraceuticals Flavorings Collagen Gelatin Enzymes …. Jónas R. Viðarsson ©Matís Key to be able to maximize value of all catches Whole fish 116 100,0% Roes / Milt 5 4,3% liver 5 4,3% Viscera 6 5,2% Head 30 25,9% Fraim 18 15,5% Pinbones & cutoffs 2 1,7% Skin 4 3,4% Bellyflap 3 2,6% Fillet 43 37,1% Jónas R.
    [Show full text]
  • 9. Palolo Swarming Previous Section | Park Home Page | Table of Contents
    previous section | park Home page | table of contents NATURAL HISTORY GUIDE 9. Palolo swarming Once or twice a year, palolo swarm to the surface of the sea in great numbers. Samoans eagerly await this night and scoop up large amounts of this delicacy along the shoreline with hand nets. This gift from the sea was traditionally greeted with necklaces made from the fragrant moso’oi flower and the night of the palolo was and still remains a happy time of celebration. The rich taste of palolo is enjoyed raw or fried with butter, onions or eggs, or spread on toast. Palolo is the edible portion of a polychaete worm (Eunice viridis) that lives in shallow coral reefs throughout the south central Pacific, although they do not swarm at all of these locations. This phenomenon is well known in Samoa, Rarotonga, Tonga, Fiji, the Solomon Islands and Vanuatu. Palolo are about 12 inches long and live in burrows dug into the coral pavement on the outer reef flat. They are composed of two distinct sections (see drawing). The front section is the basic segmented polychaete with eyes, mouth, etc., followed by a string of segments called the “epitoke” that contain reproductive gametes colored blue- green (females) or tan (males). Each epitoke segments bear a tiny eyespot that can sense light (that's why islanders are able to use a lantern to attract the palolo to their nets). When it comes time to spawn, palolo will back out of their burrows and release the epitoke section from their body. The epitokes then twirl around in the water in vast numbers and look like dancing spaghetti.
    [Show full text]
  • Sperm Features of Captive Atlantic Bluefin Tuna (Thunnus Thynnus)
    Journal of Applied Ichthyology October 2010, Volume 26, Issue 5, pages 775–778 Archimer http://dx.doi.org/10.1111/j.1439-0426.2010.01533.x http://archimer.ifremer.fr © 2010 Blackwell Verlag, Berlin The definitive version is available at http://onlinelibrary.wiley.com/ ailable on the publisher Web site Sperm features of captive Atlantic bluefin tuna (Thunnus thynnus) M. Suquet1, *, J. Cosson2, F. De La Gándara3, C.C. Mylonas4, M. Papadaki4, S. Lallemant5, C. Fauvel5 1 Ifremer, PFOM/PI, Station Expérimentale d’Argenton, Argenton, France 2 CNRS, UMR 7009, Univ. Paris VI, Station Marine, Villefranche sur mer, France 3 IEO, Centro Oceanográfico de Murcia, Puerto de Mazarrón, Murcia, Spain blisher-authenticated version is av 4 Institute of Aquaculture, Hellenic Center for Marine Research, Crete, Greece 5 Ifremer, Station Expérimentale d’Aquaculture, Palavas les Flots, France *: Corresponding author : Marc Suquet, email address : [email protected] Abstract: The present study aimed to establish some basic characteristics of Atlantic bluefin tuna sperm from captive mature males, treated or untreated by gonadotropin releasing hormones agonist (GnRHa). Intratesticular milt was collected from treated and untreated fish (mean weight ± SD: 122.9 ± 29.2 kg, n = 21). There was no significant effect of GnRHa treatment on GSI (1.33 ± 0.70%, n = 21) or on sperm concentration (3.8 ± 1.3 × 1010 spermatozoa ml−1, n = 21) estimated by optical density at 260 nm. Similarly, the percentage of motile spermatozoa measured at 30 s post activation: activating medium (AM seawater containing 10 mg ml-1 BSA) was not significantly different between control and GnRHa implanted males.
    [Show full text]
  • Cryopreservation of Lumpfish Cyclopterus Lumpus (Linnaeus, 1758) Milt
    Cryopreservation of lumpfish Cyclopterus lumpus (Linnaeus, 1758) milt Gunnvør Norgberg, Asa Johannesen and Regin Arge Fiskaaling, Aquacultural Research Station of the Faroes, vig Air,´ Hvalv´ık, Faroe Islands ABSTRACT This study has established a successful protocol to cryopreserve lumpfish Cyclopterus lumpus (Linnaeus, 1758) milt. Three cryosolutions were tested based on Mounib’s medium; the original medium including reduced l-glutathione (GSH), the basic sucrose and potassium bicarbonate medium without GSH, or with hen’s egg yolk (EY). Dimethyl sulphoxide (DMSO) was used as the cryoprotectant along with all three diluents in a 1–2 dilution. Cryopreservation was performed with the mentioned cryosolutions at two freezing rates. Motility percentages of spermatozoa were evaluated using ImageJ with a computer assisted sperm analyzer (CASA) plug-in. Findings revealed that spermatozoa cryopreserved in Mounib’s medium without GSH had a post-thaw motility score of 6.4 percentage points (pp) higher than those in the original Mounib’s medium, and an addition of EY to the modified Mounib’s medium lowered the post-thaw motility score by 19.3 pp. The diVerence in motility between both freezing rates was 13.0 pp, and samples cryopreserved on a 4.8 cm high tray resulted in a better post-thaw motility score. On average, cryopreserved milt had a 24.1 pp lower post-thaw motility score than fresh milt. There was no significant diVerence in fertilisation success between cryopreserved and fresh milt. Cryopreservation of lumpfish milt has, to our knowledge, never been successfully carried out before. The established protocol will be a main contributing factor in a stable production of lumpfish juveniles in future.
    [Show full text]
  • A Suggested Protocol for Extending Milt from Male Salmonids for Use in Wild Spawn Operations
    A suggested protocol for extending milt from male salmonids for use in wild spawn operations October 31, 2010 Kevin B. Rogers, Aquatic Research, Colorado Division of Wildlife, PO Box 775777, Steamboat Springs, CO 80477, [email protected] _______________________________________________________________________ Overview Recent interest in creating sterile hybrids (e.g. tiger trout or splake) for the Colorado Division of Wildlife has created a need to easily transport viable gametes from one body of water to another as parents often come from distant locations. The simple process of extending milt allows culturists the convenience of not having to transport live adult fish. Extended milt can also be used to easily enhance genetic diversity in bottlenecked native cutthroat trout brood stocks or help achieve adequate fertilization rates when males are scarce. The latter condition is surprisingly common in wild spawn operations, as male salmonids often arrive on the spawning grounds before females, and are often unable to produce much milt during the tail end of the run. Being able to dilute what little milt they do produce to allow fertilization of large lots of eggs can be a useful asset for these operations. Extending trout milt Collecting milt Trout semen activated by dilution with water has an extremely short life spawn with almost 90% of the motility subsiding after just 10 seconds of exposure. As such, it is extremely important that no water find its way into the extending process. Drying the vent area of ripe males with blue paper shop towels provide an inexpensive way to rapidly soak up any excess water.
    [Show full text]
  • Determining Sexual Maturity of Broodstock for Induced Spawning of Fish
    SRAC Publication No. 423 Southern Regional Aquaculture Center November 1991 Determining Sexual Maturity of Broodstock for Induced Spawning of Fish R.W. Rottmann, J.V. Shireman, and F.A. Chapman* Hormones injected for induced Sampling eggs and sperm with a microscope (e.g., 60x). The spawning of fish do not produce male is turned belly up, and the eggs and sperm (gametes); they Sampling the eggs and sperm of vent area is dried by blotting with only trigger the release of fully de- the brood fish eliminates the guess- a towel. The area just behind the veloped gametes. Fish must not work in determining the stage of pelvic fins is gently massaged to- only be sexually mature but also in sexual development. Brood fish ward the vent to strip the milt. The the advanced stage of sexual devel- must be sampled quickly and care- first few drops of milt are wiped opment before induced spawning fully to minimize physical injury away. A sample of milt is col- will be successful. and stress. The importance of lected by inserting the tip of a eye- proper handling cannot be overem- dropper into the urogenital The external appearance of brood phasized. Before sampling the opening. Suction is applied while fish has long been used to assess testes or ovaries, the fish maybe stripping to draw milt into the eye- the stage of sexual development. quieted, if necessary, with anaest- dropper. Care must be taken to in- In some species, males change in hetic such as MS-222. It is best to sure that water, urine, intestinal appearance during the spawning keep the fish in the water when contents, slime, or blood are not season (e.g., vivid breeding colors sampling.
    [Show full text]