Shovelnose Rays (Rajiformes)

Total Page:16

File Type:pdf, Size:1020Kb

Shovelnose Rays (Rajiformes) I & I NSW WILD FISHERIES RESEARCH PROGRAM Shovelnose Rays (Rajiformes) EXPLOITATION STATUS UNDEFINED Eastern shovelnose ray is by far the most significant species in the catch of this group – research underway should improve biological knowledge for this species. SCIENTIFIC NAME STANDARD NAME COMMENT Constitutes the majority of the catch of this Aptychotrema rostrata eastern shovelnose ray group. There are minor landings of this species Rhynchobatus australiae whitespotted guitarfish from northern NSW. The small catches of this species are often Trygonorrhina fasciata eastern fiddler ray discarded. Glaucostegus typus giant shovelnose ray Caught infrequently. Rhina ancylostoma shark ray Caught infrequently. Rhynchobatus australiae Image © Bernard Yau Background Eastern shovelnose rays grow to a maximum Between 100 and 150 t of ‘fiddler’ rays are length of about 100 cm and weight of about landed annually in NSW. The bulk of the 4 kg while fiddler rays reach 120 cm and about catch (estimated 75%) consists of the eastern 10 kg. The whitespotted guitarfish can attain shovelnose ray (Aptychotrema rostrata), with 300 cm in length and weigh more than 200 kg. smaller quantities (~ 20%) of the eastern fiddler ray (Trygonorrhina fasciata) and occasional The biology of the eastern shovelnose ray in landings of the large whitespotted guitarfish Moreton Bay has been studied. Both sexes (Rhynchobatus australiae), the giant shovelnose matured at around 60 cm in length, and the ray (Glaucostegus typus) and the shark ray females were found to breed annually with (Rhina ancylostoma). large specimens giving birth in the summer to as many as 18 young. New-born young are The shovelnose and fiddler rays are endemic about 20 cm long. There is little biological to the southern Queensland and NSW coasts information available for the fiddler ray (likely (between latitudes 27° and 36° S) while the to have a similar reproductive cycle to the guitarfish ranges from northern NSW through shovelnose ray) or the whitespotted guitarfish. the tropics to southern Japan. All species mainly inhabit inshore smooth sandy substrates in depths less than 100 m and almost all the catch is taken by trawlers. STATUS OF FISHERIES RESOURCES IN NSW, 2008/09 SHOVELNOSE RAYS | P 283 WILD FISHERIES RESEARCH PROGRAM The commercial catch is taken almost totally by Historical Landings of Shovelnose Rays the Ocean Trawl Fishery. Significant numbers of shovelnosed rays are also taken by recreational 150 anglers. The commercial landings have been relatively stable at around 100 to 150 t since the mid 1990s when ‘fiddler/banjo shark’ 100 and ‘shovelnose/sand shark’ were first given separate species categories on commercial catch recording forms. Landings (t) 50 The stock status of all species is uncertain and the species composition of the catch needs to be more accurately determined. New 0 catch reporting forms introduced in July 2009 90/91 92/93 94/95 96/97 98/99 00/01 02/03 04/05 06/07 08/09 require catches of all species to be separately Financial Year recorded. No stock assessment is available for Commercial landings (including available historical shovelnosed or fiddler rays in NSW waters. records) of shovelnose rays for NSW from 1990/91 to Length frequency data are available for the 2008/09 for all fishing methods. common species from Fisheries Research Vessel Kapala trawl surveys of inshore grounds in the 1990s. Landings by Commercial Fishery of Shovelnose Additional Notes Rays Ocean Trap and Line • The majority of the commercial catch is Ocean Prawn Trawl (Primary Species) eastern shovelnose ray mainly from ocean Fish Trawl (Primary Species) prawn trawling and ocean fish trawling. Shovelnose rays are also taken in significant 150 quantities by recreational fishers. • Preliminary indications are that the stock of eastern shovelnose rays is more or less stable, 100 but mortality rates are yet to be estimated. Landings (t) • Female shovelnose rays have up to 18 50 embryos and move into shallower waters over the summer months to give birth (they 0 are not susceptible to the trawl fishery during 97/98 99/00 01/02 03/04 05/06 07/08 this stage but are taken by recreational Financial Year fishers). Reported landings of shovelnose rays by NSW commercial fisheries from 1997/98. Fisheries which • These species are difficult to monitor after contribute less than 2.5% of the landings are excluded landing because fishers head and fin them. for clarity and privacy. Onboard identification of the different species is straightforward because they have distinct morphologies. Catch Rereational Catch of Shovelnose Rays The annual recreational harvest of shovelnose rays in NSW is likely to lie between 20 and 50 t. This estimate is based upon the results of the offsite National Recreational and Indigenous Fishing Survey (Henry and Lyle, 2003) and onsite surveys undertaken by I & I NSW. P 284 | SHOVELNOSE RAYS STATUS OF FISHERIES RESOURCES IN NSW, 2008/09 Catch Per Unit Effort Information of Shovelnose Further Reading Rays Harvested by Fish Trawling in NSW Ferrell, D. (1993). Pilot study on the feasibility of 1.0 ageing snapper, rubberlip morwong, red gurnard and banjo (fiddler) rays. Unpublished report. Cronulla, NSW Fisheries Research Institute: 22pp. 0.8 Henry, G.W. and J.M. Lyle (2003). The National Recreational and Indigenous Fishing Survey. Final 0.6 Report to the Fisheries Research & Development Corporation and the Fisheries Action Program 0.4 Project FRDC 1999/158. NSW Fisheries Final Report Relative Catch Rate Series No. 48. 188. pp Cronulla, NSW Fisheries. 0.2 Kyne, P.M. and M.B. Bennett (2002). Diet of the eastern shovelnose ray, Aptychotrema rostrata (Shaw & 0.0 Nodder, 1794), from Moreton Bay, Queensland, 93/94 98/99 03/04 08/09 Australia. Marine and Freshwater Research 53 (3): Financial Year 679-686. Catch rates of shovelnose rays harvested using fish Kyne, P.M. and M.B. Bennett (2002). Reproductive trawling for NSW. Two indicators are provided: (1) median biology of the eastern shovelnose ray, Aptychotrema catch rate (lower solid line); and (2) 90th percentile of the catch rate (upper dashed line). Note that catch rates rostrata (Shaw & Nodder, 1794), from Moreton are not a robust indicator of abundance in many cases. Bay, Queensland, Australia. Marine and Freshwater Caution should be applied when interpreting these Research 53 (2): 583-589. results. Last, P.R. and J.D. Stevens (2009). Sharks and Rays of Australia 2nd Edition. Melbourne, CSIRO. Marshall, L.J., W.T. White and I.C. Potter (2007). Length Frequency of Eastern Shovelnose Ray Reproductive biology and diet of the southern fiddler ray, Trygonorrhina fasciata (Batoidea : Rhinobatidae), an important trawl bycatch species. 0.14 1989/90−1995/96 Marine and Freshwater Research 58 (1): 104-115. n = 6310 0.12 0.10 Please visit the CSIRO website, 0.08 http://www.marine.csiro.au/caab/ and search for the species code (CAAB) 37 027009, 37 026001, 0.06 Proportion 37 027006 and 37 026002, common name or 0.04 scientific name to find further information. Please note that common names have been adopted from 0.02 Last and Stevens (2010) and may differ to those 0.00 contained on the CAAB website. 20 40 60 80 100 TL (cm) The length distribution of eastern shovelnose ray caught during trawl surveys by the Fisheries Research Vessel Kapala was comprised mainly of rays between 20 and 100 cm total length (TL). There is no minimum legal length for shovelnose rays in NSW. © State of New South Wales through Industry and Investment NSW 2010. You may copy, distribute and otherwise freely deal with this publication for any purpose, provided that you attribute Industry and Investment NSW as the owner. Disclaimer: The information contained in this publication is based on knowledge and understanding at the time of writing (April 2010). However, because of advances in knowledge, users are reminded of the need to ensure that information upon which they rely is up to date and to check currency of the information with the appropriate officer of Industry and Investment NSW or the user’s independent adviser. SHOVELNOSE RAYS | P 285 WILD FISHERIES RESEARCH PROGRAM P 286 | SHOVELNOSE RAYS.
Recommended publications
  • The Fishing and Illegal Trade of the Angelshark DNA Barcoding
    Fisheries Research 206 (2018) 193–197 Contents lists available at ScienceDirect Fisheries Research journal homepage: www.elsevier.com/locate/fishres The fishing and illegal trade of the angelshark: DNA barcoding against T misleading identifications ⁎ Ingrid Vasconcellos Bunholia, Bruno Lopes da Silva Ferrettea,b, , Juliana Beltramin De Biasia,b, Carolina de Oliveira Magalhãesa,b, Matheus Marcos Rotundoc, Claudio Oliveirab, Fausto Forestib, Fernando Fernandes Mendonçaa a Laboratório de Genética Pesqueira e Conservação (GenPesC), Instituto do Mar (IMar), Universidade Federal de São Paulo (UNIFESP), Santos, SP, 11070-102, Brazil b Laboratório de Biologia e Genética de Peixes (LBGP), Instituto de Biociências de Botucatu (IBB), Universidade Estadual Paulista (UNESP), Botucatu, SP, 18618-689, Brazil c Acervo Zoológico da Universidade Santa Cecília (AZUSC), Universidade Santa Cecília (Unisanta), Santos, SP, 11045-907, Brazil ARTICLE INFO ABSTRACT Handled by J Viñas Morphological identification in the field can be extremely difficult considering fragmentation of species for trade Keywords: or high similarity between congeneric species. In this context, the shark group belonging to the genus Squatina is Conservation composed of three species distributed in the southern part of the western Atlantic. These three species are Endangered species classified in the IUCN Red List as endangered, and they are currently protected under Brazilian law, which Fishing monitoring prohibits fishing and trade. Molecular genetic tools are now used for practical taxonomic identification, parti- Forensic genetics cularly in cases where morphological observation is prevented, e.g., during fish processing. Consequently, DNA fi Mislabeling identi cation barcoding was used in the present study to track potential crimes against the landing and trade of endangered species along the São Paulo coastline, in particular Squatina guggenheim (n = 75) and S.
    [Show full text]
  • Chondrichthyan Fishes (Sharks, Skates, Rays) Announcements
    Chondrichthyan Fishes (sharks, skates, rays) Announcements 1. Please review the syllabus for reading and lab information! 2. Please do the readings: for this week posted now. 3. Lab sections: 4. i) Dylan Wainwright, Thursday 2 - 4/5 pm ii) Kelsey Lucas, Friday 2 - 4/5 pm iii) Labs are in the Northwest Building basement (room B141) 4. Lab sections done: first lab this week on Thursday! 5. First lab reading: Agassiz fish story; lab will be a bit shorter 6. Office hours: we’ll set these later this week Please use the course web site: note the various modules Outline Lecture outline: -- Intro. to chondrichthyan phylogeny -- 6 key chondrichthyan defining traits (synapomorphies) -- 3 chondrichthyan behaviors -- Focus on several major groups and selected especially interesting ones 1) Holocephalans (chimaeras or ratfishes) 2) Elasmobranchii (sharks, skates, rays) 3) Batoids (skates, rays, and sawfish) 4) Sharks – several interesting groups Not remotely possible to discuss today all the interesting groups! Vertebrate tree – key ―fish‖ groups Today Chondrichthyan Fishes sharks Overview: 1. Mostly marine 2. ~ 1,200 species 518 species of sharks 650 species of rays 38 species of chimaeras Skates and rays 3. ~ 3 % of all ―fishes‖ 4. Internal skeleton made of cartilage 5. Three major groups 6. Tremendous diversity of behavior and structure and function Chimaeras Chondrichthyan Fishes: 6 key traits Synapomorphy 1: dentition; tooth replacement pattern • Teeth are not fused to jaws • New rows move up to replace old/lost teeth • Chondrichthyan teeth are
    [Show full text]
  • An Introduction to the Classification of Elasmobranchs
    An introduction to the classification of elasmobranchs 17 Rekha J. Nair and P.U Zacharia Central Marine Fisheries Research Institute, Kochi-682 018 Introduction eyed, stomachless, deep-sea creatures that possess an upper jaw which is fused to its cranium (unlike in sharks). The term Elasmobranchs or chondrichthyans refers to the The great majority of the commercially important species of group of marine organisms with a skeleton made of cartilage. chondrichthyans are elasmobranchs. The latter are named They include sharks, skates, rays and chimaeras. These for their plated gills which communicate to the exterior by organisms are characterised by and differ from their sister 5–7 openings. In total, there are about 869+ extant species group of bony fishes in the characteristics like cartilaginous of elasmobranchs, with about 400+ of those being sharks skeleton, absence of swim bladders and presence of five and the rest skates and rays. Taxonomy is also perhaps to seven pairs of naked gill slits that are not covered by an infamously known for its constant, yet essential, revisions operculum. The chondrichthyans which are placed in Class of the relationships and identity of different organisms. Elasmobranchii are grouped into two main subdivisions Classification of elasmobranchs certainly does not evade this Holocephalii (Chimaeras or ratfishes and elephant fishes) process, and species are sometimes lumped in with other with three families and approximately 37 species inhabiting species, or renamed, or assigned to different families and deep cool waters; and the Elasmobranchii, which is a large, other taxonomic groupings. It is certain, however, that such diverse group (sharks, skates and rays) with representatives revisions will clarify our view of the taxonomy and phylogeny in all types of environments, from fresh waters to the bottom (evolutionary relationships) of elasmobranchs, leading to a of marine trenches and from polar regions to warm tropical better understanding of how these creatures evolved.
    [Show full text]
  • A New Species of Wedgefish, Rhynchobatus Springeri
    Descriptions of new Borneo sharks and rays 77 $QHZVSHFLHVRIZHGJH¿VKRhynchobatus springeri 5K\QFKREDWRLGHL5K\QFKREDWLGDH IURPWKH:HVWHUQ3DFL¿F Leonard J.V. Compagno1 & Peter R. Last2 1 Shark Research Center, Iziko – Museums of Cape Town, Cape Town 8000, SOUTH AFRICA 2 CSIRO Marine & Atmospheric Research, Wealth from Oceans Flagship, GPO Box 1538, Hobart, TAS, 7001, AUSTRALIA ABSTRACT.—$QHZVSHFLHVRIZHGJH¿VKRhynchobatus springeri sp. nov. is described from specimens FROOHFWHGIURPWKH,QGR±0DOD\UHJLRQZLWKDFRQ¿UPHGUDQJHH[WHQGLQJIURPWKH*XOIRI7KDLODQGVRXWK to Java, and possibly westward to at least Sri Lanka. It is a medium-sized species to about 215 cm TL, with males reaching adulthood at about 110 cm TL. Rhynchobatus springeri closely resembles R. palpebratus in body shape and having a dark, eye-brow like marking on its orbital membrane, but differs from this species in having a lower vertebral count (113–126 vs. 130–139 total free centra), a broader preorbital snout, and more rows of white spots on the tail of adults. Other Rhynchobatus species in the region attain a much larger adult size, and have a relatively narrower snout and much higher vertebral counts. A revision of the group LVQHHGHGWR¿QGPRUHXVHIXO¿HOGFKDUDFWHUV Key words: Rhynchobatidae – Rhynchobatus springeri±%URDGQRVH:HGJH¿VK±QHZVSHFLHV±:HVWHUQ 3DFL¿F PDF contact: [email protected] INTRODUCTION Rhynchobatus by various authors, but only two, the West African R. luebberti Ehrenbaum, 1914 and the Indo– The genus Rhynchobatus Müller & Henle, 1837 :HVW3DFL¿FR. djiddensis (Forsskål, 1775), are generally comprises several species of moderate-sized to giant recognised as valid and most of the remaining taxa have (attaining between 0.8 and more than 3 m total length) been synonymised with R.
    [Show full text]
  • Classification and Systematic Arrangement
    Introduction 13 CLASSIFICATION AND SYSTEMATIC ARRANGEMENT Considering that the purpose of this document is to Class Chondrichthyes (cartilaginous fishes) provide a simple user-friendly guide for species identification, no reference will be found here to Subclass Holocephali (chimaeras) dichotomy keys for single species. It is important that the classification used in this guide be defined, Order Chimaeriformes (chimaera and silver sharks) as available literature is not always in agreement Subclass Elasmobranchii (sharks) with this presentation. The classification of this group is still under review as no consensus has Superorder Squalomorphi (squalomorph sharks) been found to reconcile different authors’ positions. Order Hexanchiformes (cow and frilled sharks) For more information and further specific details on the taxonomy and biology of cartilaginous fish Order Squaliformes (dogfish sharks) species, refer to Tortonese, 1956; Hureau and Monod 1979; Whitehead et al., 1984; Fischer et al., Order Squatiniformes (angel sharks) 1987; Fredj and Maurin, 1987; Compagno, 1988, 2005; Nelson, 1994; Shirai, 1996; Mould, 1998. The Order Pristiophoriformes (sawsharks) * consultation of FishBase http://www.fishbase.org Order Rajiformes (batoids) (Froese and Pauly, 2000) proved very useful. The most fundamental references are Compagno’s Superorder Galeomorphi (galeomorph sharks) catalogues issued in 1984 and his recent revision partially issued in 2001. Order Heterodontiformes (bullhead sharks) * This guide follows the systematic organization Order
    [Show full text]
  • The Ecology of Shark-Like Batoids: Implications for Management in the Great Barrier Reef Region
    ResearchOnline@JCU This file is part of the following reference: White, Jimmy (2014) The ecology of shark-like batoids: implications for management in the Great Barrier Reef region. PhD thesis, James Cook University. Access to this file is available from: http://researchonline.jcu.edu.au/40746/ The author has certified to JCU that they have made a reasonable effort to gain permission and acknowledge the owner of any third party copyright material included in this document. If you believe that this is not the case, please contact [email protected] and quote http://researchonline.jcu.edu.au/40746/ THE ECOLOGY OF SHARK-LIKE BATOIDS: IMPLICATIONS FOR MANAGEMENT IN THE GREAT BARRIER REEF REGION Thesis by Jimmy White B.Sc. (Hons) Submitted For the degree of Doctor of Philosophy in the School of Earth and Environmental Sciences James Cook University Townsville 1 STATEMENT OF ACCESS I, the undersigned author of this work, understand that James Cook University will make this thesis available within the University Library, and via the Australian Digital Theses network, for use elsewhere. I declare that the electronic copy of this thesis provided to the James Cook University library is an accurate copy of the print thesis submitted, within the limits of the technology available. I understand that, as an unpublished work, a these has significant protection under the Copyright Act and; All users consulting this thesis must agree not to copy or closely paraphrase it in whole or in part without the written consent of the author; and to make public written acknowledgement for any assistance which may obtain from it.
    [Show full text]
  • Florida's Fintastic Sharks and Rays Lesson and Activity Packet
    Florida's Fintastic Sharks and Rays An at-home lesson for grades 3-5 Produced by: This educational workbook was produced through the support of the Indian River Lagoon National Estuary Program. 1 What are sharks and rays? Believe it or not, they’re a type of fish! When you think “fish,” you probably picture a trout or tuna, but fishes come in all shapes and sizes. All fishes share the following key characteristics that classify them into this group: Fishes have the simplest of vertebrate hearts with only two chambers- one atrium and one ventricle. The spine in a fish runs down the middle of its back just like ours, making fish vertebrates. All fishes have skeletons, but not all fish skeletons are made out of bones. Some fishes have skeletons made out of cartilage, just like your nose and ears. Fishes are cold-blooded. Cold-blooded animals use their environment to warm up or cool down. Fins help fish swim. Fins come in pairs, like pectoral and pelvic fins or are singular, like caudal or anal fins. Later in this packet, we will look at the different types of fins that fishes have and some of the unique ways they are used. 2 Placoid Ctenoid Ganoid Cycloid Hard protective scales cover the skin of many fish species. Scales can act as “fingerprints” to help identify some fish species. There are several different scale types found in bony fishes, including cycloid (round), ganoid (rectangular or diamond), and ctenoid (scalloped). Cartilaginous fishes have dermal denticles (Placoid) that resemble tiny teeth on their skin.
    [Show full text]
  • And Giant Guitarfish (Rhynchobatus Djiddensis)
    VIRAL DISCOVERY IN BLUEGILL SUNFISH (LEPOMIS MACROCHIRUS) AND GIANT GUITARFISH (RHYNCHOBATUS DJIDDENSIS) BY HISTOPATHOLOGY EVALUATION, METAGENOMIC ANALYSIS AND NEXT GENERATION SEQUENCING by JENNIFER ANNE DILL (Under the Direction of Alvin Camus) ABSTRACT The rapid growth of aquaculture production and international trade in live fish has led to the emergence of many new diseases. The introduction of novel disease agents can result in significant economic losses, as well as threats to vulnerable wild fish populations. Losses are often exacerbated by a lack of agent identification, delay in the development of diagnostic tools and poor knowledge of host range and susceptibility. Examples in bluegill sunfish (Lepomis macrochirus) and the giant guitarfish (Rhynchobatus djiddensis) will be discussed here. Bluegill are popular freshwater game fish, native to eastern North America, living in shallow lakes, ponds, and slow moving waterways. Bluegill experiencing epizootics of proliferative lip and skin lesions, characterized by epidermal hyperplasia, papillomas, and rarely squamous cell carcinoma, were investigated in two isolated poopulations. Next generation genomic sequencing revealed partial DNA sequences of an endogenous retrovirus and the entire circular genome of a novel hepadnavirus. Giant Guitarfish, a rajiform elasmobranch listed as ‘vulnerable’ on the IUCN Red List, are found in the tropical Western Indian Ocean. Proliferative skin lesions were observed on the ventrum and caudal fin of a juvenile male quarantined at a public aquarium following international shipment. Histologically, lesions consisted of papillomatous epidermal hyperplasia with myriad large, amphophilic, intranuclear inclusions. Deep sequencing and metagenomic analysis produced the complete genomes of two novel DNA viruses, a typical polyomavirus and a second unclassified virus with a 20 kb genome tentatively named Colossomavirus.
    [Show full text]
  • Biology, Husbandry, and Reproduction of Freshwater Stingrays
    Biology, husbandry, and reproduction of freshwater stingrays. Ronald G. Oldfield University of Michigan, Department of Ecology and Evolutionary Biology Museum of Zoology, 1109 Geddes Ave., Ann Arbor, MI 48109 U.S.A. E-mail: [email protected] A version of this article was published previously in two parts: Oldfield, R.G. 2005. Biology, husbandry, and reproduction of freshwater stingrays I. Tropical Fish Hobbyist. 53(12): 114-116. Oldfield, R.G. 2005. Biology, husbandry, and reproduction of freshwater stingrays II. Tropical Fish Hobbyist. 54(1): 110-112. Introduction In the freshwater aquarium, stingrays are among the most desired of unusual pets. Although a couple species have been commercially available for some time, they remain relatively uncommon in home aquariums. They are often avoided by aquarists due to their reputation for being fragile and difficult to maintain. As with many fishes that share this reputation, it is partly undeserved. A healthy ray is a robust animal, and problems are often due to lack of a proper understanding of care requirements. In the last few years many more species have been exported from South America on a regular basis. As a result, many are just recently being captive bred for the first time. These advances will be making additional species of freshwater stingray increasingly available in the near future. This article answers this newly expanded supply of wild-caught rays and an anticipated increased The underside is one of the most entertaining aspects of a availability of captive-bred specimens by discussing their stingray. In an aquarium it is possible to see the gill slits and general biology, husbandry, and reproduction in order watch it eat, as can be seen in this Potamotrygon motoro.
    [Show full text]
  • Life-History Characteristics of the Eastern Shovelnose Ray, Aptychotrema Rostrata (Shaw, 1794), from Southern Queensland, Australia
    CSIRO PUBLISHING Marine and Freshwater Research, 2021, 72, 1280–1289 https://doi.org/10.1071/MF20347 Life-history characteristics of the eastern shovelnose ray, Aptychotrema rostrata (Shaw, 1794), from southern Queensland, Australia Matthew J. Campbell A,B,C, Mark F. McLennanA, Anthony J. CourtneyA and Colin A. SimpfendorferB AQueensland Department of Agriculture and Fisheries, Agri-Science Queensland, Ecosciences Precinct, GPO Box 267, Brisbane, Qld 4001, Australia. BCentre for Sustainable Tropical Fisheries and Aquaculture and College of Science and Engineering, James Cook University, 1 James Cook Drive, Townsville, Qld 4811, Australia. CCorresponding author. Email: [email protected] Abstract. The eastern shovelnose ray (Aptychotrema rostrata) is a medium-sized coastal batoid endemic to the eastern coast of Australia. It is the most common elasmobranch incidentally caught in the Queensland east coast otter trawl fishery, Australia’s largest penaeid-trawl fishery. Despite this, age and growth studies on this species are lacking. The present study estimated the growth parameters and age-at-maturity for A. rostrata on the basis of sampling conducted in southern Queensland, Australia. This study showed that A. rostrata exhibits slow growth and late maturity, which are common life- history strategies among elasmobranchs. Length-at-age data were analysed within a Bayesian framework and the von Bertalanffy growth function (VBGF) best described these data. The growth parameters were estimated as L0 ¼ 193 mm À1 TL, k ¼ 0.08 year and LN ¼ 924 mm TL. Age-at-maturity was found to be 13.3 years and 10.0 years for females and males respectively. The under-sampling of larger, older individuals was overcome by using informative priors, reducing bias in the growth and maturity estimates.
    [Show full text]
  • Age, Growth and Reproductive Biology of Two Endemic Demersal
    ZOOLOGIA 37: e49318 ISSN 1984-4689 (online) zoologia.pensoft.net RESEARCH ARTICLE Age, growth and reproductive biology of two endemic demersal bycatch elasmobranchs: Trygonorrhina fasciata and Dentiraja australis (Chondrichthyes: Rhinopristiformes, Rajiformes) from Eastern Australia Marcelo Reis1 , Will F. Figueira1 1University of Sydney, School of Life and Environmental Sciences. Edgeworth David Building (A11), Room 111, Sydney, NSW 2006, Australia. [email protected] Corresponding author: Marcelo Reis ([email protected]) http://zoobank.org/51FFF676-C96D-4B1A-A713-15921D9844BF ABSTRACT. Bottom-dwelling elasmobranchs, such as guitarfishes, skates and stingrays are highly susceptible species to bycatch due to the overlap between their distribution and area of fishing operations. Catch data for this group is also often merged in generic categories preventing species-specific assessments. Along the east coast of Australia, the Eastern Fiddler Ray, Trygonorrhina fasciata (Muller & Henle, 1841), and the Sydney Skate, Dentiraja australis (Macleay, 1884), are common components of bycatch yet there is little information about their age, growth and reproductive timing, making impact assessment difficult. In this study the age and growth (from vertebral bands) as well as reproductive parameters of these two species are estimated and reported based on 171 specimens of Eastern Fiddler Rays (100 females and 71 males) and 81 Sydney Skates (47 females and 34 males). Based on von Bertalanffy growth curve fits, Eastern Fiddler Rays grew to larger sizes than Sydney Skate but did so more slowly (ray: L∞ = 109.61, t0 = 0.26 and K = 0.20; skate: L∞ = 51.95, t0 = -0.99 and K = 0.34 [both sexes combined]). Both species had higher liver weight ratios (HSI) during austral summer.
    [Show full text]
  • Guitarfish, Glaucostegus Cemiculus & G. Granulatus Wedgefish
    EXPERT PANEL SUMMARY Proposals: 43 + 44 Guitarfish, Glaucostegus cemiculus & G. granulatus Wedgefish, Rhynchobatus australiae & R. djiddensis Insufficient Data to make a CITES determination F. Carocci F. G. cemiculus Source: F. Carocci F. G. granulatus Source: F. Carocci F. R. australiae Source: F. Carocci F. R. djiddensis Source: The guitarfish (upper panels There was evidence that wedgefish insufficient to above) and wedgefish (lower Blackchin guitarfish, G. establish declines over the full panels above) are shallow- c e m i c u l u s , a n d o t h e r species range, either for the water coastal species, recog- guitarfish have been extir- long- or short- term rate of nized by the Expert Panel as pated in the northwestern decline, as required to make a being of low-to-medium pro- Mediterranean part of their determination against the ductivity. range. Elsewhere there was CITES criteria. local evidence of long-term The Expert Panel looked for declines guitarfish catches in In considering whether to list stock status information Senegal, but numerical evi- these species, the Expert across the species' range, dence on a larger scale was Panel recommends that bearing in mind the proposal's lacking. CITES parties take note of the argument of high levels of widespread lack of manage- decline. The Expert Panel For wedgefish, the Expert ment in the fisheries taking the noted that population esti- Panel had access to addi- species and the very high mates do not exist for these tional catch datasets from value of the products (fins) in species and stock assess- India and Indonesia, which international trade.
    [Show full text]