Winter Flounder (Pleuronectes Americanus)
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Pleuronectidae, Poecilopsettidae, Achiridae, Cynoglossidae
1536 Glyptocephalus cynoglossus (Linnaeus, 1758) Pleuronectidae Witch flounder Range: Both sides of North Atlantic Ocean; in the western North Atlantic from Strait of Belle Isle to Cape Hatteras Habitat: Moderately deep water (mostly 45–330 m), deepest in southern part of range; found on mud, muddy sand or clay substrates Spawning: May–Oct in Gulf of Maine; Apr–Oct on Georges Bank; Feb–Jul Meristic Characters in Middle Atlantic Bight Myomeres: 58–60 Vertebrae: 11–12+45–47=56–59 Eggs: – Pelagic, spherical Early eggs similar in size Dorsal fin rays: 97–117 – Diameter: 1.2–1.6 mm to those of Gadus morhua Anal fin rays: 86–102 – Chorion: smooth and Melanogrammus aeglefinus Pectoral fin rays: 9–13 – Yolk: homogeneous Pelvic fin rays: 6/6 – Oil globules: none Caudal fin rays: 20–24 (total) – Perivitelline space: narrow Larvae: – Hatching occurs at 4–6 mm; eyes unpigmented – Body long, thin and transparent; preanus length (<33% TL) shorter than in Hippoglossoides or Hippoglossus – Head length increases from 13% SL at 6 mm to 22% SL at 42 mm – Body depth increases from 9% SL at 6 mm to 30% SL at 42 mm – Preopercle spines: 3–4 occur on posterior edge, 5–6 on lateral ridge at about 16 mm, increase to 17–19 spines – Flexion occurs at 14–20 mm; transformation occurs at 22–35 mm (sometimes delayed to larger sizes) – Sequence of fin ray formation: C, D, A – P2 – P1 – Pigment intensifies with development: 6 bands on body and fins, 3 major, 3 minor (see table below) Glyptocephalus cynoglossus Hippoglossoides platessoides Total myomeres 58–60 44–47 Preanus length <33%TL >35%TL Postanal pigment bars 3 major, 3 minor 3 with light scattering between Finfold pigment Bars extend onto finfold None Flexion size 14–20 mm 9–19 mm Ventral pigment Scattering anterior to anus Line from anus to isthmus Early Juvenile: Occurs in nursery habitats on continental slope E. -
Aspects of the Life History of Hornyhead Turbot, Pleuronichthys Verticalis, Off Southern California
Aspects of the Life History of Hornyhead Turbot, Pleuronichthys verticalis, off Southern California he hornyhead turbot T(Pleuronichthys verticalis) is a common resident flatfish on the mainland shelf from Magdalena Bay, Baja Califor- nia, Mexico to Point Reyes, California (Miller and Lea 1972). They are randomly distributed over the bottom at a density of about one fish per 130 m2 and lie partially buried in the sediment (Luckinbill 1969). Hornyhead turbot feed primarily on sedentary, tube-dwelling polychaetes (Luckinbill 1969, Allen 1982, Cross et al. 1985). They pull the tubes from the sediment, Histological section of a fish ovary. extract the polychaete, and then eject the tube (Luckinbill 1969). Hornyhead turbot are Orange County, p,p’-DDE Despite the importance of batch spawners and may averaged 362 μg/kg wet the hornyhead turbot in local spawn year round (Goldberg weight in hornyhead turbot monitoring programs, its life 1982). Their planktonic eggs liver and 5 μg/kg dry weight in history has received little are 1.00-1.16 mm diameter the sediments (CSDOC 1992). attention. The long-term goal (Sumida et al. 1979). Their In the same year in Santa of our work is to determine larvae occur in the nearshore Monica Bay, p,p’-DDE aver- how a relatively low trophic plankton throughout the year aged 7.8 mg/kg wet weight in level fish like the hornyhead (Gruber et al. 1982, Barnett et liver and 81 μg/kg dry weight turbot accumulates tissue al. 1984, Moser et al. 1993). in the sediments (City of Los levels of chlorinated hydrocar- Several agencies in South- Angeles 1992). -
Age, Growth and Population Dynamics of Lemon Sole Microstomus Kitt(Walbaum 1792)
Age, growth and population dynamics of lemon sole Microstomus kitt (Walbaum 1792) sampled off the west coast of Ireland By Joan F. Hannan Masters Thesis in Fish Biology Galway-Mayo Institute of Technology Supervisors of Research Dr. Pauline King and Dr. David McGrath Submitted to the Higher Education and Training Awards Council July 2002 Age, growth and population dynamics of lemon sole Microstomus kitt (Walbaum 1792) sampled off the west coast of Ireland Joan F. Hannan ABSTRACT The age, growth, maturity and population dynamics o f lemon sole (Microstomus kitt), captured off the west coast o f Ireland (ICES division Vllb), were determined for the period November 2000 to February 2002. The maximum age recorded was 14 years. Males o f the population were dominated by 4 year olds, while females were dominated by 5 year olds. Females dominated the sex ratio in the overall sample, each month sampled, at each age and from 22cm in total length onwards (when N > 20). Possible reasons for the dominance o f females in the sex ratio are discussed. Three models were used to obtain the parameters o f the von Bertalanfly growth equation. These were the Ford-Walford plot (Beverton and Holt 1957), the Gulland and Holt plot (1959) and the Rafail (1973) method. Results o f the fitted von Bertalanffy growth curves showed that female lemon sole o ff the west coast o f Ireland grew faster than males and attained a greater size. Male and female lemon sole mature from 2 years o f age onwards. There is evidence in the population o f a smaller asymptotic length (L«, = 34.47cm), faster growth rate (K = 0.1955) and younger age at first maturity, all o f which are indicative o f a decrease in population size, when present results are compared to data collected in the same area 22 years earlier. -
Identification of Larvae of Three Arctic Species of Limanda (Family Pleuronectidae)
Identification of larvae of three arctic species of Limanda (Family Pleuronectidae) Morgan S. Busby, Deborah M. Blood & Ann C. Matarese Polar Biology ISSN 0722-4060 Polar Biol DOI 10.1007/s00300-017-2153-9 1 23 Your article is protected by copyright and all rights are held exclusively by 2017. This e- offprint is for personal use only and shall not be self-archived in electronic repositories. If you wish to self-archive your article, please use the accepted manuscript version for posting on your own website. You may further deposit the accepted manuscript version in any repository, provided it is only made publicly available 12 months after official publication or later and provided acknowledgement is given to the original source of publication and a link is inserted to the published article on Springer's website. The link must be accompanied by the following text: "The final publication is available at link.springer.com”. 1 23 Author's personal copy Polar Biol DOI 10.1007/s00300-017-2153-9 ORIGINAL PAPER Identification of larvae of three arctic species of Limanda (Family Pleuronectidae) 1 1 1 Morgan S. Busby • Deborah M. Blood • Ann C. Matarese Received: 28 September 2016 / Revised: 26 June 2017 / Accepted: 27 June 2017 Ó Springer-Verlag GmbH Germany 2017 Abstract Identification of fish larvae in Arctic marine for L. proboscidea in comparison to the other two species waters is problematic as descriptions of early-life-history provide additional evidence suggesting the genus Limanda stages exist for few species. Our goal in this study is to may be paraphyletic, as has been proposed in other studies. -
Greenland Turbot Assessment
6HFWLRQ STOCK ASSESSMENT OF GREENLAND TURBOT James N. Ianelli, Thomas K. Wilderbuer, and Terrance M. Sample 6XPPDU\ Changes to this year’s assessment in the past year include: 1. new summary estimates of retained and discarded Greenland turbot by different target fisheries, 2. update the estimated catch levels by gear type in recent years, and 3. new length frequency and biomass data from the 1998 NMFS eastern Bering Sea shelf survey. Conditions do not appear to have changed substantively over the past several years. For example, the abundance of Greenland turbot from the eastern Bering Sea (EBS) shelf-trawl survey has found only spotty quantities with very few small fish that were common in the late 1970s and early 1980s. The majority of the catch has shifted to longline gear in recent years. The assessment model analysis was similar to last year but with a slightly higher estimated overall abundance. We attribute this to a slightly improved fit to the longline survey data trend. The target stock size (B40%, female spawning biomass) is estimated at about 139,000 tons while the projected 1999 spawning biomass is about 110,000 tons. The adjusted yield projection from F40% computations is estimated at 20,000 tons for 1999, and increase of 5,000 from last year’s ABC. Given the continued downward abundance trend and no sign of recruitment to the EBS shelf, extra caution is warranted. We therefore recommend that the ABC be set to 15,000 tons (same value as last year). As additional survey information become available and signs of recruitment (perhaps from areas other than the shelf) are apparent, then we believe that the full ABC or increases in harvest may be appropriate for this species. -
Fish Bulletin 161. California Marine Fish Landings for 1972 and Designated Common Names of Certain Marine Organisms of California
UC San Diego Fish Bulletin Title Fish Bulletin 161. California Marine Fish Landings For 1972 and Designated Common Names of Certain Marine Organisms of California Permalink https://escholarship.org/uc/item/93g734v0 Authors Pinkas, Leo Gates, Doyle E Frey, Herbert W Publication Date 1974 eScholarship.org Powered by the California Digital Library University of California STATE OF CALIFORNIA THE RESOURCES AGENCY OF CALIFORNIA DEPARTMENT OF FISH AND GAME FISH BULLETIN 161 California Marine Fish Landings For 1972 and Designated Common Names of Certain Marine Organisms of California By Leo Pinkas Marine Resources Region and By Doyle E. Gates and Herbert W. Frey > Marine Resources Region 1974 1 Figure 1. Geographical areas used to summarize California Fisheries statistics. 2 3 1. CALIFORNIA MARINE FISH LANDINGS FOR 1972 LEO PINKAS Marine Resources Region 1.1. INTRODUCTION The protection, propagation, and wise utilization of California's living marine resources (established as common property by statute, Section 1600, Fish and Game Code) is dependent upon the welding of biological, environment- al, economic, and sociological factors. Fundamental to each of these factors, as well as the entire management pro- cess, are harvest records. The California Department of Fish and Game began gathering commercial fisheries land- ing data in 1916. Commercial fish catches were first published in 1929 for the years 1926 and 1927. This report, the 32nd in the landing series, is for the calendar year 1972. It summarizes commercial fishing activities in marine as well as fresh waters and includes the catches of the sportfishing partyboat fleet. Preliminary landing data are published annually in the circular series which also enumerates certain fishery products produced from the catch. -
American Sole (Family Achiridae) Diversity in North Carolina
American Sole (Family Achiridae) Diversity in North Carolina Along North Carolina’s shore there are three families of flatfish comprising five or six species having eyes on the right side of their body facing upward when lying in or atop the substrate (NCFishes.com; Tracy et al. 2020; Table 1; Figure 1). The families and species can be confusing to tell apart. The key characteristics provided in Table 1 should enable one to differentiate between the three families and this document will aid you in the identification of three species in the Family Achiridae (American Soles) in North Carolina. Generally, soles are small, flat, right-facing fishes (i.e., the left side of the body is on the substrate) with small, minute eyes and of little commercial or recreational value (Rohde et al. 2009). Table 1. The three families of right-facing flatfish found along and off the coast of North Carolina. Common Key Characteristics No. Family Name (adapted from Kells and Carpenter (2014); Munroe (2002a; 2002b)) Species • Preopercular margin not free, concealed by skin or represented only by a naked superficial groove. • Dorsal fin extending forward well in advance of eyes, the anterior rays concealed within a fleshy dermal envelope and difficult to see. Achiridae Soles • Lateral line essentially straight, without high arch over pectoral fin; often indistinct, but most readily seen on the eyed side, usually crossed at right angles by accessory branches (achirine lines) extending toward dorsal and anal fins; • Urinary papilla on eyed side. 2 or 3 • Preopercular margin free, not covered with skin and scales. -
Recycled Fish Sculpture (.PDF)
Recycled Fish Sculpture Name:__________ Fish: are a paraphyletic group of organisms that consist of all gill-bearing aquatic vertebrate animals that lack limbs with digits. At 32,000 species, fish exhibit greater species diversity than any other group of vertebrates. Sculpture: is three-dimensional artwork created by shaping or combining hard materials—typically stone such as marble—or metal, glass, or wood. Softer ("plastic") materials can also be used, such as clay, textiles, plastics, polymers and softer metals. They may be assembled such as by welding or gluing or by firing, molded or cast. Researched Photo Source: Alaskan Rainbow STEP ONE: CHOOSE one fish from the attached Fish Names list. Trout STEP TWO: RESEARCH on-line and complete the attached K/U Fish Research Sheet. STEP THREE: DRAW 3 conceptual sketches with colour pencil crayons of possible visual images that represent your researched fish. STEP FOUR: Once your fish designs are approved by the teacher, DRAW a representational outline of your fish on the 18 x24 and then add VALUE and COLOUR . CONSIDER: Individual shapes and forms for the various parts you will cut out of recycled pop aluminum cans (such as individual scales, gills, fins etc.) STEP FIVE: CUT OUT using scissors the various individual sections of your chosen fish from recycled pop aluminum cans. OVERLAY them on top of your 18 x 24 Representational Outline 18 x 24 Drawing representational drawing to judge the shape and size of each piece. STEP SIX: Once you have cut out all your shapes and forms, GLUE the various pieces together with a glue gun. -
WINTER FLOUNDER / Pseudopleuronectes Americanus (Walbaum 1792) / Blackback, Georges Bank Flounder, Lemon Sole, Rough Flounder / Bigelow and Schroeder 1953:276-283
WINTER FLOUNDER / Pseudopleuronectes americanus (Walbaum 1792) / Blackback, Georges Bank Flounder, Lemon Sole, Rough Flounder / Bigelow and Schroeder 1953:276-283 Description. Body oval, about two and a quarter times as long to base of caudal fin as it is wide, thick-bodied, and with a proportionately broader caudal peduncle and tail than any of the other local small flatfishes (Fig. 305). Mouth small, not gaping back to eye, lips thick and fleshy. Blind side of each jaw armed with one series of close-set incisor-like teeth. Eyed side with only a few teeth, or even toothless. Dorsal fin originates opposite forward edge of upper eye, of nearly equal height throughout its length. Anal fin highest about midway, preceded by a short, sharp spine (postabdominal bone). Pelvic fins alike on both sides of body, separated from long anal fin by a considerable gap. Gill rakers short and conical. Lateral line nearly straight, with a slight bow above pectoral fin. Scales rough on eyed side, including interorbital space; smooth on blind side in juveniles and mature females, rough in mature males when rubbed Georges Bank fish of 63.5 cm, weighing 3.6 kg. The NEFSC from caudal peduncle toward head. An occasional large adult female groundfish bottom trawl survey collected two 64-cm females, one on may also be rough ventrally. 22 October 1986 at 42°67' N, 67°32' W and a second on 15 Apri11997 at 41°01' N, 68°25'W (R. Brown, pers. comm., 25 Sept. Meristics. Dorsal fin rays 59-76; anal fin rays 44-58; pectoral fin 1998). -
Intrinsic Vulnerability in the Global Fish Catch
The following appendix accompanies the article Intrinsic vulnerability in the global fish catch William W. L. Cheung1,*, Reg Watson1, Telmo Morato1,2, Tony J. Pitcher1, Daniel Pauly1 1Fisheries Centre, The University of British Columbia, Aquatic Ecosystems Research Laboratory (AERL), 2202 Main Mall, Vancouver, British Columbia V6T 1Z4, Canada 2Departamento de Oceanografia e Pescas, Universidade dos Açores, 9901-862 Horta, Portugal *Email: [email protected] Marine Ecology Progress Series 333:1–12 (2007) Appendix 1. Intrinsic vulnerability index of fish taxa represented in the global catch, based on the Sea Around Us database (www.seaaroundus.org) Taxonomic Intrinsic level Taxon Common name vulnerability Family Pristidae Sawfishes 88 Squatinidae Angel sharks 80 Anarhichadidae Wolffishes 78 Carcharhinidae Requiem sharks 77 Sphyrnidae Hammerhead, bonnethead, scoophead shark 77 Macrouridae Grenadiers or rattails 75 Rajidae Skates 72 Alepocephalidae Slickheads 71 Lophiidae Goosefishes 70 Torpedinidae Electric rays 68 Belonidae Needlefishes 67 Emmelichthyidae Rovers 66 Nototheniidae Cod icefishes 65 Ophidiidae Cusk-eels 65 Trachichthyidae Slimeheads 64 Channichthyidae Crocodile icefishes 63 Myliobatidae Eagle and manta rays 63 Squalidae Dogfish sharks 62 Congridae Conger and garden eels 60 Serranidae Sea basses: groupers and fairy basslets 60 Exocoetidae Flyingfishes 59 Malacanthidae Tilefishes 58 Scorpaenidae Scorpionfishes or rockfishes 58 Polynemidae Threadfins 56 Triakidae Houndsharks 56 Istiophoridae Billfishes 55 Petromyzontidae -
An Industrial Survey for Associated Species
FISHING FOR KNOWLEDGE An industrial survey for associated species Report of Project Phase I by Anne Doeksen and Karin van der Reijden A collaboration between The North Sea Foundation & IMARES Commissioned by EKOFISH Group June 2014 Content 1 Introduction ......................................................................................................................... 3 2 Fisheries Management for associated stocks ............................................................................. 4 2.1 Management of associated species ................................................................................. 4 2.2 Managing associated species under the new CFP .............................................................. 8 2.3 Key insights and Conclusive points ............................................................................... 10 3 Stock assessments ............................................................................................................. 12 3.1 How to do a stock assessment ..................................................................................... 12 3.2 Surveys for stock assessment ...................................................................................... 13 3.3 Data availability and knowledge gaps for associated species ............................................. 14 3.4 Key insights and concluding points ............................................................................... 15 4 References ....................................................................................................................... -
Guide to the Coastal Marine Fishes of California
STATE OF CALIFORNIA THE RESOURCES AGENCY DEPARTMENT OF FISH AND GAME FISH BULLETIN 157 GUIDE TO THE COASTAL MARINE FISHES OF CALIFORNIA by DANIEL J. MILLER and ROBERT N. LEA Marine Resources Region 1972 ABSTRACT This is a comprehensive identification guide encompassing all shallow marine fishes within California waters. Geographic range limits, maximum size, depth range, a brief color description, and some meristic counts including, if available: fin ray counts, lateral line pores, lateral line scales, gill rakers, and vertebrae are given. Body proportions and shapes are used in the keys and a state- ment concerning the rarity or commonness in California is given for each species. In all, 554 species are described. Three of these have not been re- corded or confirmed as occurring in California waters but are included since they are apt to appear. The remainder have been recorded as occurring in an area between the Mexican and Oregon borders and offshore to at least 50 miles. Five of California species as yet have not been named or described, and ichthyologists studying these new forms have given information on identification to enable inclusion here. A dichotomous key to 144 families includes an outline figure of a repre- sentative for all but two families. Keys are presented for all larger families, and diagnostic features are pointed out on most of the figures. Illustrations are presented for all but eight species. Of the 554 species, 439 are found primarily in depths less than 400 ft., 48 are meso- or bathypelagic species, and 67 are deepwater bottom dwelling forms rarely taken in less than 400 ft.