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Diet of Wahoo, Acanthocybium Solandri, from the Northcentral Gulf of Mexico
Diet of Wahoo, Acanthocybium solandri, from the Northcentral Gulf of Mexico JAMES S. FRANKS, ERIC R. HOFFMAYER, JAMES R. BALLARD1, NIKOLA M. GARBER2, and AMBER F. GARBER3 Center for Fisheries Research and Development, Gulf Coast Research Laboratory, The University of Southern Mississippi, P.O. Box 7000, Ocean Springs, Mississippi 39566 USA 1Department of Coastal Sciences, The University of Southern Mississippi, P.O. Box 7000, Ocean Springs, Mississippi 39566 USA 2U.S. Department of Commerce, NOAA Sea Grant, 1315 East-West Highway, Silver Spring, Maryland 20910 USA 3Huntsman Marine Science Centre, 1Lower Campus Road, St. Andrews, New Brunswick, Canada E5B 2L7 ABSTRACT Stomach contents analysis was used to quantitatively describe the diet of wahoo, Acanthocybium solandri, from the northcen- tral Gulf of Mexico. Stomachs were collected opportunistically from wahoo (n = 321) that were weighed (TW, kg) and measured (FL, mm) at fishing tournaments during 1997 - 2007. Stomachs were frozen and later thawed for removal and preservation (95% ethanol) of contents to facilitate their examination and identification. Empty stomachs (n = 71) comprised 22% of the total collec- tion. Unfortunately, the preserved, un-examined contents from 123 stomachs collected prior to Hurricane Katrina (August 2005) were destroyed during the hurricane. Consequently, assessments of wahoo stomach contents reported here were based on the con- tents of the 65 ‘pre-Katrina’ stomachs, in addition to the contents of 62 stomachs collected ‘post-Katrina’ during 2006 and 2007, for a total of 127 stomachs. Wahoo with prey in their stomachs ranged 859 - 1,773 mm FL and 4.4 - 50.4 kg TW and were sexed as: 31 males, 91 females and 5 sex unknown. -
Assessment of Indian Ocean Narrow-Barred Spanish Mackerel (Scomberomorus Commerson) Using Data
IOTC–2017–WPNT07–17 Rev_1 Assessment of Indian Ocean narrow-barred Spanish mackerel (Scomberomorus commerson) using data limited catch-based methods June 2017 IOTC Secretariat1 Introduction ......................................................................................................................................... 2 Basic biology .................................................................................................................................. 2 Fisheries and Catch Trends ............................................................................................................. 2 Methods .............................................................................................................................................. 6 1) C-MSY method ....................................................................................................................... 6 2) Optimised Catch Only Method (OCOM) ................................................................................ 8 Results ................................................................................................................................................. 9 Catch-MSY method ........................................................................................................................ 9 OCOM method .............................................................................................................................. 14 Discussion ........................................................................................................................................ -
Chub Mackerel, Scomber Japonicus (Perciformes: Scombridae), a New Host Record for Nerocila Phaiopleura (Isopoda: Cymothoidae)
生物圏科学 Biosphere Sci. 56:7-11 (2017) Chub mackerel, Scomber japonicus (Perciformes: Scombridae), a new host record for Nerocila phaiopleura (Isopoda: Cymothoidae) 1) 2) Kazuya NAGASAWA * and Hiroki NAKAO 1) Graduate School of Biosphere Science, Hiroshima University, 1-4-4 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8528, Japan 2) Fisheries Research Division, Oita Prefectural Agriculture, Forestry and Fisheries Research Center, Kamiura, Saeki, Oita 879-2602, Japan Abstract An ovigerous female of Nerocila phaiopleura Bleeker, 1857 was collected from the caudal peduncle of a chub mackerel, Scomber japonicus Houttuyn, 1782 (Perciformes: Scombridae), at the Hōyo Strait located between the western Seto Inland Sea and the Bungo Channell in western Japan. This represents a new host record for N. phaioplueura and its fourth record from the Seto Inland Sea and adjacent region. Key words: Cymothoidae, fish parasite, Isopoda, Nerocila phaiopleura, new host record, Scomber japonicus INTRODUCTION The Hōyo Strait is located between the western Seto Inland Sea and the Bungo Channell in western Japan. This strait is famous as a fishing ground of two perciform fishes of high quality, viz., chub mackerel, Scomber japonicus Houttuyn, 1782 (Scombridae), and Japanese jack mackerel, Trachurus japonicus (Temminck and Schlegel, 1844) (Carangidae), both of which are currently called“ Seki-saba” and“ Seki-aji”, respectively, as registered brands (e.g., Ishida and Fukushige, 2010). The brand names are well known nationwide, and the price of the fishes is very high (up to 5,000 yen per kg). Under these situations, the fishermen working in the strait pay much attention to the parasites of the fishes they catch because those fishes are almost exclusively eaten raw as“ sashimi.” Recently, a chub mackerel infected by a large parasite on the body surface (Fig. -
Assessment of Indian Ocean Narrow-Barred Spanish Mackerel (Scomberomorus Commerson) Using Data- Limited Methods
IOTC–2020–WPNT10–14 Assessment of Indian Ocean narrow-barred Spanish mackerel (Scomberomorus commerson) using data- limited methods 30th June 2020 Dan, Fu1 1. Introduction ................................................................................................................................. 2 2. Basic Biology .............................................................................................................................. 2 3. Catch, CPUE and Fishery trends................................................................................................. 2 4. Methods....................................................................................................................................... 5 4.1. C-MSY method ....................................................................................................................... 6 4.2. Bayesian Schaefer production model (BSM) .......................................................................... 7 5. Results ......................................................................................................................................... 8 5.1. C-MSY method ................................................................................................................... 8 5.2. Bayesian Schaefer production model (BSM) .................................................................... 11 6. Discussion ............................................................................................................................. 17 References ........................................................................................................................................ -
Fisheries of the Northeast
FISHERIES OF THE NORTHEAST AMERICAN BLUE LOBSTER BILLFISHES ATLANTIC COD MUSSEL (Blue marlin, Sailfish, BLACK SEA BASS Swordfish, White marlin) CLAMS DRUMS BUTTERFISH (Arc blood clam, Arctic surf clam, COBIA Atlantic razor clam, Atlantic surf clam, (Atlantic croaker, Black drum, BLUEFISH (Gulf butterfish, Northern Northern kingfish, Red drum, Northern quahog, Ocean quahog, harvestfish) CRABS Silver sea trout, Southern kingfish, Soft-shelled clam, Stout razor clam) (Atlantic rock crab, Blue crab, Spot, Spotted seatrout, Weakfish) Deep-sea red crab, Green crab, Horseshoe crab, Jonah crab, Lady crab, Northern stone crab) GREEN SEA FLATFISH URCHIN EELS (Atlantic halibut, American plaice, GRAY TRIGGERFISH HADDOCK (American eel, Fourspot flounder, Greenland halibut, Conger eel) Hogchoker, Southern flounder, Summer GROUPERS flounder, Winter flounder, Witch flounder, (Black grouper, Yellowtail flounder) Snowy grouper) MACKERELS (Atlantic chub mackerel, MONKFISH HAKES JACKS Atlantic mackerel, Bullet mackerel, King mackerel, (Offshore hake, Red hake, (Almaco jack, Amberjack, Bar Silver hake, Spotted hake, HERRINGS jack, Blue runner, Crevalle jack, Spanish mackerel) White hake) (Alewife, Atlantic menhaden, Atlantic Florida pompano) MAHI MAHI herring, Atlantic thread herring, Blueback herring, Gizzard shad, Hickory shad, Round herring) MULLETS PORGIES SCALLOPS (Striped mullet, White mullet) POLLOCK (Jolthead porgy, Red porgy, (Atlantic sea Scup, Sheepshead porgy) REDFISH scallop, Bay (Acadian redfish, scallop) Blackbelly rosefish) OPAH SEAWEEDS (Bladder -
© Iccat, 2007
A5 By-catch Species APPENDIX 5: BY-CATCH SPECIES A.5 By-catch species By-catch is the unintentional/incidental capture of non-target species during fishing operations. Different types of fisheries have different types and levels of by-catch, depending on the gear used, the time, area and depth fished, etc. Article IV of the Convention states: "the Commission shall be responsible for the study of the population of tuna and tuna-like fishes (the Scombriformes with the exception of Trichiuridae and Gempylidae and the genus Scomber) and such other species of fishes exploited in tuna fishing in the Convention area as are not under investigation by another international fishery organization". The following is a list of by-catch species recorded as being ever caught by any major tuna fishery in the Atlantic/Mediterranean. Note that the lists are qualitative and are not indicative of quantity or mortality. Thus, the presence of a species in the lists does not imply that it is caught in significant quantities, or that individuals that are caught necessarily die. Skates and rays Scientific names Common name Code LL GILL PS BB HARP TRAP OTHER Dasyatis centroura Roughtail stingray RDC X Dasyatis violacea Pelagic stingray PLS X X X X Manta birostris Manta ray RMB X X X Mobula hypostoma RMH X Mobula lucasana X Mobula mobular Devil ray RMM X X X X X Myliobatis aquila Common eagle ray MYL X X Pteuromylaeus bovinus Bull ray MPO X X Raja fullonica Shagreen ray RJF X Raja straeleni Spotted skate RFL X Rhinoptera spp Cownose ray X Torpedo nobiliana Torpedo -
Biological Aspects of Spotted Seerfish Scomberomorus Guttatus
CORE Metadata, citation and similar papers at core.ac.uk Provided by CMFRI Digital Repository Indian J. Fish., 65(2): 42-49, 2018 42 DOI: 10.21077/ijf.2018.65.2.65436-05 Biological aspects of spotted seerfish Scomberomorus guttatus (Bloch & Schneider, 1801) (Scombridae) from north-eastern Arabian Sea C. ANULEKSHMI*, J. D. SARANG, S. D. KAMBLE, K. V. AKHILESH, V. D. DESHMUKH AND V. V. SINGH ICAR-Central Marine Fisheries Research Institute, Mumbai Research Centre, Fisheries University Road Versova, Andheri (W), Mumbai - 400 061, Maharashtra, India e-mail: [email protected] ABSTRACT Spotted seerfishScomberomorus guttatus (Bloch & Schneider, 1801) is one of the highly priced table fishes in India, which contributed 4.7% of all India scombrid fishery with 17,684 t landed in 2014. Its fishery is dominant in the Arabian Sea and northern Arabian Sea contributed 62% to India’s spotted seerfish fishery. Biological information on S. guttatus is scarce and the same was studied during the period 2010-2014 from Maharashtra coast, north-eastern Arabian Sea. A total of 930 specimens (185-550 mm FL) collected from commercial landings were used for the study. Length-weight relation of pooled sexes was estimated as log (W) = -3.1988+2.66074 log (L) (r2 = 0.93). Fishery was dominated by males with the sex ratio -1 of 0.76:1. Relative fecundity ranged from 105-343 eggs g of bodyweight. The length at first maturity (Lm) was estimated to be 410 mm TL for females. Mature and gravid females were dominant in May and August-November. Dietary studies (% IRI) showed dominance of Acetes spp. -
Spanish Mackerel J
2.1.10.6 SSM CHAPTER 2.1.10.6 AUTHORS: LAST UPDATE: ATLANTIC SPANISH MACKEREL J. VALEIRAS and E. ABAD Sept. 2006 2.1.10.6 Description of Atlantic Spanish Mackerel (SSM) 1. Names 1.a Classification and taxonomy Species name: Scomberomorus maculatus (Mitchill 1815) ICCAT species code: SSM ICCAT names: Atlantic Spanish mackerel (English), Maquereau espagnol (French), Carita del Atlántico (Spanish) According to Collette and Nauen (1983), the Atlantic Spanish mackerel is classified as follows: • Phylum: Chordata • Subphylum: Vertebrata • Superclass: Gnathostomata • Class: Osteichthyes • Subclass: Actinopterygii • Order: Perciformes • Suborder: Scombroidei • Family: Scombridae 1.b Common names List of vernacular names used according to ICCAT, FAO and Fishbase (www.fishbase.org). The list is not exhaustive and some local names might not be included. Barbados: Spanish mackerel. Brazil: Sororoca. China: ᶷᩬ㤿㩪. Colombia: Sierra. Cuba: Sierra. Denmark: Plettet kongemakrel. Former USSR: Ispanskaya makrel, Korolevskaya pyatnistaya makrel, Pyatnistaya makrel. France: Thazard Atlantique, Thazard blanc. Germany: Gefleckte Königsmakrele. Guinea: Makréni. Italy: Sgombro macchiato. Martinique: Taza doré, Thazard tacheté du sud. Mexico: Carite, Pintada, Sierra, Sierra común. Poland: Makrela hiszpanska. Portugal: Serra-espanhola. Russian Federation: Ispanskaya makrel, Korolevskaya pyatnistaya makrel, Pyatnistaya makrel; ɦɚɤɪɟɥɶ ɢɫɩɚɧɫɤɚɹ. South Africa: Spaanse makriel, Spanish mackerel. Spain: Carita Atlántico. 241 ICCAT MANUAL, 1st Edition (January 2010) Sweden: Fläckig kungsmakrill. United Kingdom: Atlantic spanish mackerel. United States of America: Spanish mackerel. Venezuela: Carite, Sierra pintada. 2. Identification Figure 1. Drawing of an adult Atlantic Spanish mackerel (by A. López, ‘Tokio’). Characteristics of Scomberomorus maculatus (see Figure 1 and Figure 2) Atlantic Spanish mackerel is a small tuna species. Maximum size is 91 cm fork length and 5.8 kg weight (IGFA 2001). -
Gill Specializations in High-Performance Pelagic Teleosts, with Reference to Striped Marlin (Tetrapturus Audax) and Wahoo (Acanthocybium Solandri)
BULLETIN OF MARINE SCIENCE, 79(3): 747–759, 2006 Gill SPecialiZations in HigH-Performance Pelagic teleosts, WitH reference to striPED marlin (TETRAPTURUS AUDAX) anD WAHoo (ACANTHOCYBIUM SOLANDRI) Nicholas C. Wegner, Chugey A. Sepulveda, and Jeffrey B. Graham Abstract Analysis of the gill structure of striped marlin, Tetrapturus audax (Philippi, 1887), and wahoo, Acanthocybium solandri (Cuvier, 1832), demonstrates similari- ties to tunas (family Scombridae) in the presence of gill specializations to maintain rigidity during fast, sustainable swimming and to permit the O2 uptake required by high aerobic performance. For ram-gill ventilators such as tunas, wahoo, and striped marlin, a rigid gill structure prevents lamellar deformation during fast wa- ter flow. In tunas, lamellar fusions bind adjacent lamellae on the same filament to opposing lamellae of the neighboring filament. Examination of striped marlin and wahoo gill structure demonstrates a previously undescribed inter-lamellar fusion which binds juxtaposed lamellae on the same filament, but does not connect to op- posing lamellae of the adjacent filament. Lamellar thicknesses and the water-blood barrier distances in striped marlin and wahoo are comparable to those of tunas and among the smallest recorded. Vascular replica casts reveal that striped marlin lamellar vascular channels are similar to tunas in having a diagonal progression that reduces lamellar vascular resistance. Wahoo lamellar channels, however, have a linear pattern similar to most other teleosts. Tunas, bonitos, mackerels (family Scombridae), and billfishes (families Istiophori- dae, Xiphiidae) are highly specialized for fast, continuous swimming. Both groups are ram ventilators [i.e., their nonstop movement forces water over the gills thus replacing active gill ventilation (Jones and Randall, 1978; Roberts and Rowell, 1988)] which, at faster swimming speeds, reduces drag associated with cyclic jaw move- ments for respiration (Brown and Muir, 1970; Freadman, 1981). -
Small-Scale Patterns in Distribution and Feeding of Atlantic Mackerel (Scomber Scombrus L.) Larvae in the Celtic Sea with Special Regard to Intra-Cohort Cannibalism
Helgol Mar Res (2001) 55:135–149 DOI 10.1007/s101520000068 ORIGINAL ARTICLE Nicola Hillgruber · Matthias Kloppmann Small-scale patterns in distribution and feeding of Atlantic mackerel (Scomber scombrus L.) larvae in the Celtic Sea with special regard to intra-cohort cannibalism Received: 9 August 2000 / Received in revised form: 31 October 2000 / Accepted: 12 November 2000 / Published online: 10 March 2001 © Springer-Verlag and AWI 2001 Abstract Short-term variability in vertical distribution cannibalism, reaching >50% body dry weight in larva and feeding of Atlantic mackerel (Scomber scombrus L.) ≥8.0 mm SL. larvae was investigated while tracking a larval patch over a 48-h period. The patch was repeatedly sampled Keywords Mackerel larvae · Vertical distribution · Diet · and a total of 12,462 mackerel larvae were caught within Diel patterns · Cannibalism the upper 100 m of the water column. Physical parame- ters were monitored at the same time. Larval length dis- tribution showed a mode in the 3.0 mm standard length Introduction (SL) class (mean abundance of 3.0 mm larvae x¯ =75.34 per 100 m3, s=34.37). Highest densities occurred at In the eastern Atlantic, the highest densities of Atlantic 20–40 m depth. Larvae <5.0 mm SL were highly aggre- mackerel (Scomber scombrus) larvae appear in the Celtic gated above the thermocline, while larvae ≥5.0 mm SL Sea and above the Celtic Shelf in May/June (O’Brien were more dispersed and tended to migrate below the and Fives 1995), where the larvae hatch at the onset of thermocline. Gut contents of 1,177 mackerel larvae the secondary productivity maximum (Colebrook 1986) (2.9–9.7 mm SL) were analyzed. -
SPAWNING BEHAVIOUR and FECUNDITY of the INDIAN MACKEREL, RASTRELLIGER KANAGURTA (CUVIER), at MANGALORE Central Marine Fisheries
CORE Metadata, citation and similar papers at core.ac.uk Provided by CMFRI Digital Repository SPAWNING BEHAVIOUR AND FECUNDITY OF THE INDIAN MACKEREL, RASTRELLIGER KANAGURTA (CUVIER), AT MANGALORE V. RAMAMOHANA RAO Central Marine Fisheries Research Institute; Sub-station, Visakhapatnam-3 The earliest reference to the fecundity of the Indian mackerel was by Devanesan and John (1940) who estimated the number of ripe eggs in the mackerel ovary as 94,000. Subsequent work was directed mostly towards finding out the spawning behaviour of this fish, by the study of the intra-ovarian eggs. Pradhan (1956) indicated the possibility of the Indian mackerel spawning the eggs in successive batches over a prolonged period, like its Atlantic counter-part Scomber scombrus (L). Pra dhan and Palekar (1956) described the maturity stages I to VII, based on the external appearance of the ovary, its size relative to the abdominal cavity, and the range of ova-diameter readings. However, they have not given any ova-diameter frequency polygons. Sekharan (1958) studied the ova-diameter frequency in a few ovaries of the mackerel, ranging in maturity stage from II-III to V-VI, VI-VII and a few spent ovaries. He stated that his investigation showed a possibility of the mackerel eggs ripening in batches and of their release in succession. Radhakrishnan (1962), adopting the method followed by Clark (1934), Prabhu (1956), and Qasim and Qayyam (1961), studied the ova-diameter frequency seasonally and indicated the possibility of the mackerel shedding its eggs in batches. Vijayaraghavan (1962) followed a different procedure. Employing very high magnification, he measured ova with diameter greater than 0.525 mm. -
Investigations on the Biology of Indian Mackerel Rastrelliger Kanagurta
Investigations on the biology of Indian Mackerel Rastrelliger kanagurta (Cuvier) along the Central Kerala coast with special reference to maturation, feeding and lipid dynamics Thesis submitted to Cochin University of Science and Technology in partial fulfillment of the requirement for the degree of DOCTOR OF PHILOSOPHY FACULTY OF MARINE SCIENCES GANGA .U. Reg. No. 2763 DEPARTMENT OF MARINE BIOLOGY, MICROBIOLOGY AND BIOCHEMISTRY SCHOOL OF MARINE SCIENCES COCHIN UNIVERSITY OF SCIENCE AND TECHNOLOGY KOCHI – 682 016, INDIA September 2010 DECLARATION I, Ganga. U., do hereby declare that the thesis entitled “Investigations on the biology of Indian Mackerel Rastrelliger kanagurta (Cuvier) along the Central Kerala coast with special reference to maturation, feeding and lipid dynamics “ is a genuine record of research work carried out by me under the guidance of Prof. (Dr.) C.K. Radhakrishnan, Emeritus Professor, Cochin University of Science and Technology, and no part of the work has previously formed the basis for the award of any Degree, Associateship and Fellowship or any other similar title or recognition of any University or Institution. Ganga.U Kochi – 16 September-2010 CERTIFICATE This is to certify that the thesis entitled “Investigations on the biology of Indian Mackerel Rastrelliger kanagurta (Cuvier) along the Central Kerala coast with special reference to maturation, feeding and lipid dynamics” to be submitted by Smt. Ganga. U., is an authentic record of research work carried out by her under my guidance and supervision in partial fulfilment of the requirement for the degree of Doctor of Philosophy of Cochin University of Science and Technology, under the faculty of Marine Sciences.