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A Classification of Living and Fossil Genera of Decapod Crustaceans
RAFFLES BULLETIN OF ZOOLOGY 2009 Supplement No. 21: 1–109 Date of Publication: 15 Sep.2009 © National University of Singapore A CLASSIFICATION OF LIVING AND FOSSIL GENERA OF DECAPOD CRUSTACEANS Sammy De Grave1, N. Dean Pentcheff 2, Shane T. Ahyong3, Tin-Yam Chan4, Keith A. Crandall5, Peter C. Dworschak6, Darryl L. Felder7, Rodney M. Feldmann8, Charles H. J. M. Fransen9, Laura Y. D. Goulding1, Rafael Lemaitre10, Martyn E. Y. Low11, Joel W. Martin2, Peter K. L. Ng11, Carrie E. Schweitzer12, S. H. Tan11, Dale Tshudy13, Regina Wetzer2 1Oxford University Museum of Natural History, Parks Road, Oxford, OX1 3PW, United Kingdom [email protected] [email protected] 2Natural History Museum of Los Angeles County, 900 Exposition Blvd., Los Angeles, CA 90007 United States of America [email protected] [email protected] [email protected] 3Marine Biodiversity and Biosecurity, NIWA, Private Bag 14901, Kilbirnie Wellington, New Zealand [email protected] 4Institute of Marine Biology, National Taiwan Ocean University, Keelung 20224, Taiwan, Republic of China [email protected] 5Department of Biology and Monte L. Bean Life Science Museum, Brigham Young University, Provo, UT 84602 United States of America [email protected] 6Dritte Zoologische Abteilung, Naturhistorisches Museum, Wien, Austria [email protected] 7Department of Biology, University of Louisiana, Lafayette, LA 70504 United States of America [email protected] 8Department of Geology, Kent State University, Kent, OH 44242 United States of America [email protected] 9Nationaal Natuurhistorisch Museum, P. O. Box 9517, 2300 RA Leiden, The Netherlands [email protected] 10Invertebrate Zoology, Smithsonian Institution, National Museum of Natural History, 10th and Constitution Avenue, Washington, DC 20560 United States of America [email protected] 11Department of Biological Sciences, National University of Singapore, Science Drive 4, Singapore 117543 [email protected] [email protected] [email protected] 12Department of Geology, Kent State University Stark Campus, 6000 Frank Ave. -
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Contributions to Zoology, 67 (4) 223-235 (1998) SPB Academic Publishing bv, Amsterdam Optics and phylogeny: is there an insight? The evolution of superposition eyes in the Decapoda (Crustacea) Edward Gaten Department of Biology, University’ ofLeicester, Leicester LEI 7RH, U.K. E-mail: [email protected] Keywords: Compound eyes, superposition optics, adaptation, evolution, decapod crustaceans, phylogeny Abstract cannot normally be predicted by external exami- nation alone, and usually microscopic investiga- This addresses the of structure and in paper use eye optics the tion of properly fixed optical elements is required construction of and crustacean phylogenies presents an hypoth- for a complete diagnosis. This largely rules out esis for the evolution of in the superposition eyes Decapoda, the use of fossil material in the based the of in comparatively on distribution eye types extant decapod fami- few lies. It that arthropodan specimens where the are is suggested reflecting superposition optics are eyes symplesiomorphic for the Decapoda, having evolved only preserved (Glaessner, 1969), although the optics once, probably in the Devonian. loss of Subsequent reflecting of some species of trilobite have been described has superposition optics occurred following the adoption of a (Clarkson & Levi-Setti, 1975). Also the require- new habitat (e.g. Aristeidae,Aeglidae) or by progenetic paedo- ment for good fixation and the fact that complete morphosis (Paguroidea, Eubrachyura). examination invariably involves the destruction of the specimen means that museum collections Introduction rarely reveal enough information to define the optics unequivocally. Where the optics of the The is one of the compound eye most complex component parts of the eye are under investiga- and remarkable not on of its fixation organs, only account tion, specialised to preserve the refrac- but also for the optical precision, diversity of tive properties must be used (Oaten, 1994). -
Grazing by Pyrosoma Atlanticum (Tunicata, Thaliacea) in the South Indian Ocean
MARINE ECOLOGY PROGRESS SERIES Vol. 330: 1–11, 2007 Published January 25 Mar Ecol Prog Ser OPENPEN ACCESSCCESS FEATURE ARTICLE Grazing by Pyrosoma atlanticum (Tunicata, Thaliacea) in the south Indian Ocean R. Perissinotto1,*, P. Mayzaud2, P. D. Nichols3, J. P. Labat2 1School of Biological & Conservation Sciences, G. Campbell Building, University of KwaZulu-Natal, Howard College Campus, Durban 4041, South Africa 2Océanographie Biochimique, Observatoire Océanologique, LOV-UMR CNRS 7093, BP 28, 06230 Villefranche-sur-Mer, France 3Commonwealth Scientific and Industrial Research Organisation (CSIRO), Marine and Atmospheric Research, Castray Esplanade, Hobart, Tasmania 7001, Australia ABSTRACT: Pyrosomas are colonial tunicates capable of forming dense aggregations. Their trophic function in the ocean, as well as their ecology and physiology in general, are extremely poorly known. During the ANTARES-4 survey (January and February 1999) their feeding dynamics were investigated in the south Indian Ocean. Results show that their in situ clearance rates may be among the highest recorded in any pelagic grazer, with up to 35 l h–1 per colony (length: 17.9 ± 4.3 [SD] cm). Gut pigment destruction rates, estimated for the first time in this tunicate group, are higher than those previously measured in salps and appendiculari- ans, ranging from 54 to virtually 100% (mean: 79.7 ± 19.8%) of total pigment ingested. Although individual colony ingestion rates were high (39.6 ± 17.3 [SD] µg –1 The pelagic tunicate Pyrosoma atlanticum conducts diel pigment d ), the total impact on the phytoplankton vertical migrations. Employing continuous jet propulsion, its biomass and production in the Agulhas Front was rela- colonies attain clearance rates that are among the highest in tively low, 0.01 to 4.91% and 0.02 to 5.74% respec- any zooplankton grazer. -
Annotated Checklist of New Zealand Decapoda (Arthropoda: Crustacea)
Tuhinga 22: 171–272 Copyright © Museum of New Zealand Te Papa Tongarewa (2011) Annotated checklist of New Zealand Decapoda (Arthropoda: Crustacea) John C. Yaldwyn† and W. Richard Webber* † Research Associate, Museum of New Zealand Te Papa Tongarewa. Deceased October 2005 * Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington, New Zealand ([email protected]) (Manuscript completed for publication by second author) ABSTRACT: A checklist of the Recent Decapoda (shrimps, prawns, lobsters, crayfish and crabs) of the New Zealand region is given. It includes 488 named species in 90 families, with 153 (31%) of the species considered endemic. References to New Zealand records and other significant references are given for all species previously recorded from New Zealand. The location of New Zealand material is given for a number of species first recorded in the New Zealand Inventory of Biodiversity but with no further data. Information on geographical distribution, habitat range and, in some cases, depth range and colour are given for each species. KEYWORDS: Decapoda, New Zealand, checklist, annotated checklist, shrimp, prawn, lobster, crab. Contents Introduction Methods Checklist of New Zealand Decapoda Suborder DENDROBRANCHIATA Bate, 1888 ..................................... 178 Superfamily PENAEOIDEA Rafinesque, 1815.............................. 178 Family ARISTEIDAE Wood-Mason & Alcock, 1891..................... 178 Family BENTHESICYMIDAE Wood-Mason & Alcock, 1891 .......... 180 Family PENAEIDAE Rafinesque, 1815 .................................. -
De Grave & Fransen. Carideorum Catalogus
De Grave & Fransen. Carideorum catalogus (Crustacea: Decapoda). Zool. Med. Leiden 85 (2011) 407 Fig. 48. Synalpheus hemphilli Coutière, 1909. Photo by Arthur Anker. Synalpheus iphinoe De Man, 1909a = Synalpheus Iphinoë De Man, 1909a: 116. [8°23'.5S 119°4'.6E, Sapeh-strait, 70 m; Madura-bay and other localities in the southern part of Molo-strait, 54-90 m; Banda-anchorage, 9-36 m; Rumah-ku- da-bay, Roma-island, 36 m] Synalpheus iocasta De Man, 1909a = Synalpheus Iocasta De Man, 1909a: 119. [Makassar and surroundings, up to 32 m; 0°58'.5N 122°42'.5E, west of Kwadang-bay-entrance, 72 m; Anchorage north of Salomakiëe (Damar) is- land, 45 m; 1°42'.5S 130°47'.5E, 32 m; 4°20'S 122°58'E, between islands of Wowoni and Buton, northern entrance of Buton-strait, 75-94 m; Banda-anchorage, 9-36 m; Anchorage off Pulu Jedan, east coast of Aru-islands (Pearl-banks), 13 m; 5°28'.2S 134°53'.9E, 57 m; 8°25'.2S 127°18'.4E, an- chorage between Nusa Besi and the N.E. point of Timor, 27-54 m; 8°39'.1 127°4'.4E, anchorage south coast of Timor, 34 m; Mid-channel in Solor-strait off Kampong Menanga, 113 m; 8°30'S 119°7'.5E, 73 m] Synalpheus irie MacDonald, Hultgren & Duffy, 2009: 25; Figs 11-16; Plate 3C-D. [fore-reef (near M1 chan- nel marker), 18°28.083'N 77°23.289'W, from canals of Auletta cf. sycinularia] Synalpheus jedanensis De Man, 1909a: 117. [Anchorage off Pulu Jedan, east coast of Aru-islands (Pearl- banks), 13 m] Synalpheus kensleyi (Ríos & Duffy, 2007) = Zuzalpheus kensleyi Ríos & Duffy, 2007: 41; Figs 18-22; Plate 3. -
Further Records of Penaeoidea from the East Coast of South Africa
Further records of Penaeoidea from the East coast of South Africa w. Emmerson Department of Zoology, University of Port Elizabeth, Port Elizabeth Fifty-four specimens of ten penaeoid species were Identified. Apart from commercial operations, Penaeoidea have Of particular interest was the finding of pelagic juveniles of been described and collected from South African waters two species, Funchalia (Funchalia) vil/osa and Penaeus since the beginning of this century (Stebbing 1914; marginatus. CaIman 1925; Barnard 1947, 1950; Joubert & Davies S. Afr. J. Zool. 1981,16: 132 -136 1966; Kensley 1968, 1969, 1977; Champion 1973; Ivanov Vier-en-vyftig eksemplare van tien Penaeoldea-spesies is & Hassan 1976b)_ The aim of the present work is to ge"identifiseer. Die voorkoms van onvolwasse individue van die record new localities for a clearer knowledge of distribu twee spesies Funchalia (Funchalia) vil/osa en Penaeus tion, especially for recently recorded species such as marginatus was van besondere belang. Aristeus virilis and Funchalia (Funchalia) vi/losa (Kensley S.-Afr. Tydskr. Dlerk. 1981, 16: 132 -136 1977), and to contribute to juvenile pelagic penaeoid ecology, of which very little is known_ The specimens are lodged in the South African Museum, Cape Town. ) 0 1 0 Methods 2 d A number of penaeoids were collected between 1967 and e t a 1973, mainly by trawlers operating off Durban, at depths d ( between 92 and 700 m with mesh diameters of 2,5 (ex r e ploratory) to 12,5 (commercial) cm_ Fifty-four specimens h s i of 10 penaeoid species were identified. The classification l b system used was that established by Perez Farfante u P (1977a) where previous subfamilies are elevated to e families of the superfamily Penaeoidea. -
The Family Penaeidae(Excluding Genus Penaeus)
SOUTH AFRICAN ASSOCIATION FOR MARINE BIOLOGICAL RESEARCH OCEANOGRAPHIC RESEARCH INSTITUTE Investigational Report No. 58 Th£ Penaeoidea of southeast Africa — The Family Penaeidae (excluding Genus Penaeus) by A.J. de Freitas The Investigational Report series of the Oceanographic Research Institute presents the detailed results of marine biological research. Reports have appeared at irregular intervals since 1961. All manuscripts are submitted for peer review, to national or overseas referees. The Bulletin series of the South African Association for. Marine Biological Research is of general interest and reviews the research and curatorial activities of the Oceanographic Research Institute, Aquarium and Dolphinarium. It is published annually. Both series are available in exchange for relevant publications of other scientific institutions anywhere in the world. All correspondence in this regard should be directed to: The Librarian, Oceanographic Research Institute. P.O. Box 10712. Marine Parade. 4056. Durban. South Africa. SOUTH AFRICAN ASSOCIATION FOR MARINE BIOLOGICAL RESEARCH OCEANOGRAPHIC RESEARCH INSTITUTE Investigational Report No.58 The Penaeoidea of southeast Africa. The Family Penaeidae (excluding Genus Penaeus) by A.J. de Freitas Published by THE OCEANOGRAPHIC RESEARCH INSTITUTE P.O. BOX 10712, MARINE PARADE DURBAN, 4056 SOUTH AFRICA November 1987 Copyright ISBN 0 86989 034 4 ISSN 0078-320X THE PENAEOIDEA OF SOUTHEAST AFRICA: III. The Family Penaeidae (excluding Genus Penaeus) by A.J. DE FREITAS ABSTRACT This is the third monograph of a series of five on the Penaeoidea of southeast Africa and, together with monograph four, deals with the family Penaeidae. The family is represented by nine genera of which eight, with a total of 15 species, are dealt with in this article. -
Indicative of an Offshore Migration of Females for the Purpose of Spawning During Autumn and Winter
indicative of an offshore migration of females for the purpose of spawning during autumn and winter. However, although this is possible, the facts, including the predominance of impregnated females during summer, within Maputo Bay, seems to favour the idea that a considerable degree of spawning occurs during most of the year, within the Bay. The scarcity of impregnated females on the other hand may favour migration. The fact that the period of spawning activity is so long may indicate that a mature female spawns repeatedly during her lifetime. This could explain the presence, in the population, of large females (Lc = 39-40 mm and larger) with undeveloped ovaries (Stage I) (Fig. 111-29). These are very probably females with ovaries in the process of regeneration after spawning. No work on the planktonic larval forms was carried out in Mozambique. It is therefore impossible to claim with any certainty that M. monoceros spawns within Maputo Bay, in spite of the evidence given above. Panikkar and Aiyar (1939) did suggest that M. monoceros bred in the backwater areas and Menon (1951) states that "Penaeid prawns with the exception of M. stebbingi and M. monoceros breed, as far as is known, only in the sea." This implies that M. monoceros may breed in backwater areas. However, George and George (1964) claim that"... the presence of mature adults in a sand area at a depth of 50 to 60 metres off Cochin points to this as a possible spawning ground." In September 1972 off Moma in central Mozambique, in catches predominantly of mating Penaeus indicus, a considerable number of large M. -
Decapoda, Dendrobranchiata, Penaeidae) from the Pacific Coast of Mexico
ABNORMAL ROSTRUM AND TELSON IN TWO SPECIES OF PENAEID SHRIMP (DECAPODA, DENDROBRANCHIATA, PENAEIDAE) FROM THE PACIFIC COAST OF MEXICO BY HUGO AGUIRRE1) and MICHEL E. HENDRICKX2,3) 1) Instituto Nacional de la Pesca, Centro Regional de Investigación Pesquera, P.O. Box 1177, Mazatlán, Sinaloa 82000, Mexico 2) Laboratorio de Invertebrados Bentónicos, Unidad Académica Mazatlán, Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México, P.O. Box 811, Mazatlán, Sinaloa 82000, Mexico ABSTRACT Morphological abnormalities were observed in two specimens of penaeid shrimp collected along the east coast of the Gulf of California, Mexico. A bifid rostrum was observed in the brown shrimp, Farfantepenaeus californiensis and a bifid telson in the white shrimp, Litopenaeus vannamei. RÉSUMÉ Des anomalies morphologiques ont été observées chez deux spécimens de crevettes Pénéides recoltées le long de la côte est du golfe de Californie, Mexique. La crevette brune, Farfantepenaeus californiensis, présente un rostre bifide et la crevette blanche, Litopenaeus vannamei,untelson bifide. INTRODUCTION AND MATERIAL Morphological abnormalities have long been noticed among decapod crus- taceans. These include malformations in appendages or body segments (Lucas, 1844; Le Senechal, 1888; Richard, 1893; Fauvel, 1900; Santana et al., 1990), du- plication of structures (Carvacho, 1988; Williams, 1988; Rudolph, 1996; Nakatani et al., 1997) or lack of such structures (Kulkarni et al., 1980), and reversal of asym- metry (Nouvel, 1944; Lemaitre et al., 1982; Stevens & Munk, 1991). Some defor- mities are related to bilateral gynandromorphy (Micheli, 1991). Malformations of 3) e-mail: [email protected] © Koninklijke Brill NV, Leiden, 2005 Crustaceana 78 (1): 113-119 Also available online: www.brill.nl 114 HUGO AGUIRRE & MICHEL E. -
Systematics and Extended Distribution of Metapenaeus Elegans De Man, 1907 in Coastal Water of India
Examines in Marine CRIMSON PUBLISHERS C Wings to the Research Biology & Oceanography ISSN 2578-031X Research Article Systematics and Extended Distribution of Metapenaeus elegans De Man, 1907 in Coastal Water of India Angsuman Chanda* Raja NL Khan Women’s College, Midnapur West Bengal, India *Corresponding author: Angsuman Chanda, Department of Zoology, Raja NL Khan Women’s College, Midnapur, Paschim Medinipur-721102, West Bengal, India Submission: May 12, 2018 ; Published: May 26, 2018 Abstract Present study reveals that the prawn Metapenaeus elegans is an established species. The species has been described from Menado, Celebes during reported from Andaman water by several authors. During the present study the species has been recorded from Andhra Pradesh coastal water of India. As“Siboga such Expedition”present study by extends De Man. the Silas distribution and Muthu range has reportedof the species the species up to coastal first time water from of IndianAndaman main Sea land. of Indian water. Still date the species has been Keywords: Metapenaeus elegans, Distribution, Andaman, Andhra Pradesh Introduction the prawn taxonomy is an essential prerequisite for their proper Prawn is the most valuable marine resource of many nation and management and exploitation. Fabricius [10] is the pioneer worker contribute a lion share to the economy of the country. Exploitation on prawn taxonomy in Indian water. Some important contributions of prawn resource from the seas around each country is playing on the prawns of this region during nineteenth century were by Milne Edwards [11], Miers [12], Bate [13], Wood-Mason [14], [1-4]. Recently, though there is some ecological hazard in prawn increasingly significant role in furthering their national economy Wood-Mason & Alcock [15], Alcock & Anderson [16,17]. -
Distribution, Associations and Role in the Biological Carbon Pump of Pyrosoma Atlanticum (Tunicata, Thaliacea) of Cabo Verde, NE Atlantic Vanessa I
www.nature.com/scientificreports OPEN Distribution, associations and role in the biological carbon pump of Pyrosoma atlanticum (Tunicata, Thaliacea) of Cabo Verde, NE Atlantic Vanessa I. Stenvers1,2,3*, Helena Hauss1, Karen J. Osborn2,4, Philipp Neitzel1, Véronique Merten1, Stella Scheer1, Bruce H. Robison4, Rui Freitas5 & Henk Jan T. Hoving1* Gelatinous zooplankton are increasingly acknowledged to contribute signifcantly to the carbon cycle worldwide, yet many taxa within this diverse group remain poorly studied. Here, we investigate the pelagic tunicate Pyrosoma atlanticum in the waters surrounding the Cabo Verde Archipelago. By using a combination of pelagic and benthic in situ observations, sampling, and molecular genetic analyses (barcoding, eDNA), we reveal that: P. atlanticum abundance is most likely driven by local island- induced productivity, that it substantially contributes to the organic carbon export fux and is part of a diverse range of biological interactions. Downward migrating pyrosomes actively transported an estimated 13% of their fecal pellets below the mixed layer, equaling a carbon fux of 1.96–64.55 mg C m−2 day−1. We show that analysis of eDNA can detect pyrosome material beyond their migration range, suggesting that pyrosomes have ecological impacts below the upper water column. Moribund P. atlanticum colonies contributed an average of 15.09 ± 17.89 (s.d.) mg C m−2 to the carbon fux reaching the island benthic slopes. Our pelagic in situ observations further show that P. atlanticum formed an abundant substrate in the water column (reaching up to 0.28 m2 substrate area per m2), with animals using pyrosomes for settlement, as a shelter and/or a food source. -
Funchalia Woodwardi Johnson, 1868
1 La funchalie de Woodward Funchalia woodwardi Johnson, 1868 Citation de cette fiche : Noël P., 2015. La funchalie de Woodward Funchalia woodwardi Johnson, 1868. in Muséum national d'Histoire naturelle [Ed.], 1er décembre 2015. Inventaire national du Patrimoine naturel, pp. 1-6, site web http://inpn.mnhn.fr Contact de l'auteur : Pierre Noël, SPN et DMPA, Muséum national d'Histoire naturelle, 43 rue Buffon (CP 48), 75005 Paris ; e-mail [email protected] Résumé Le tégument de cette espèce est revêtu d'une pilosité courte. Le rostre est légèrement relevé à son extrémité et diminue régulièrement de taille de sa base vers son apex. Il atteint la moitié proximale du 2e article du pédoncule antennulaire et porte dorsalement 11 à 13 dents dont 2 sont post-orbitales ; sa marge inférieure est inerme. La carapace présente de fortes carènes. Le branchiostégite porte une épine antennaire forte, une épine hépatique et une épine ptérigostomienne. Les segments abdominaux 4, 5 et 6 ont une paire de carènes latérales fortes et une autre carène dorsale médiane ; le 6e segment porte une épine à la fin de la carène dorsale et une autre plus petite sur les angles infralatéraux. Les pinces des trois premières paires de péréiopodes sont allongées, sub- cylindriques, creusées à l'intérieur. Des épipodites sont présents sur les 3 premières paires de pattes. La longueur totale atteint 173 mm. L'espèce est jaune-orangé avec des zones écarlate sur le céphalothorax ; elle se rencontre soit de façon isolée dans la colonne d'eau soit en essaim près de la surface. Les poissons bathypélagiques sont ses principaux prédateurs.