An Updated Checklist of Polychaetes (Animalia, Annelida, Polychaeta) from Odisha and West Bengal Coasts

Total Page:16

File Type:pdf, Size:1020Kb

An Updated Checklist of Polychaetes (Animalia, Annelida, Polychaeta) from Odisha and West Bengal Coasts Indian Journal of Geo Marine Sciences Vol. 50 (06), June 2021, pp. 507-510 Supplementary Data An updated checklist of polychaetes (Animalia, Annelida, Polychaeta) from Odisha and West Bengal coasts S Balakrishnan* & P C Tudu Zoological Survey of India, Marine Aquarium & Regional Centre, Digha, West Bengal – 721 428, India *[E-mail: [email protected]] Sr. No Contents Page No. 1 Table S1 — An updated checklist of polychaetes from Odisha and West Bengal coasts ii 2 Table S2 — Checklist of taxonomic accepted and unaccepted names of polychaetes viii from Odisha and West Bengal coastal waters 3 Supplementary References ix ii INDIAN J GEO-MAR SCI, VOL 50, NO 06, JUNE 2021 Supplementary Tables Table S1 — An updated checklist of polychaetes from Odisha and West Bengal coasts S. No. Order Family Species Location 1. AMPHINOMID AMPHINOMIDAE Amphinome rostrata (Pallas, 1766) Puri1 A Lamarck, 1818 2. Chloeia parva Baird, 1868 Udayapur*, Digha coast, Sagar Island, Talsari, Mouth of Hughli River, Chandipur, Balasore, Odisha1,3,4 3. Chloeia rosea Potts, 1909 Digha coast*3 4. Chloeia flava (Pallas, 1766) Odisha coast5 5. Cryptonome parvecarunculata (Horst, 1912) Sundarban, Chilka lake1,6 6. Eurythoe complanata (Pallas, 1766) Sundarban6 7. CAPITELLIDA CAPITELLIDAE Barantolla sculpta (Southern, 1921) West Bengal7 Grube, 1862 8. Capitella capitata (Fabricius, 1780) Matla river & Sundarban3,6 9. Heteromastus similis Southern, 1921 Chilka Lake7 10. Notomastus latericeus Sars, 1851 Sundarban6 11. Notomastus aberans Day, 1957 Sundarban6 12. Notomastus giganteus Moore, 1906 Off Puri8 13. Parheteromastus tenuis Monro, 1937 Sagar Island, Namkhana & Bakkhali3 14. ORBINIIDAE Hartman, Orbinia cuvieripersica (Fauvel, 1932) West Bengal8 1942 15. Aricia exarmata Fauvel, 1932 West Bengal8 16. Scoloplos sagarensis (Misra, 1999) Ganga sagar9 17. Scoloplos (Scolopolos) sagarensis Misra, 1999 Sagar Island3 18. Scoloplos (Scoloplos) marsupialis (Southern, Chilka lake1,12 1921) 19. EUNICIDA EUNICIDAE Berthold, Marphysa sanguinea (Montagu, 1813) Sagar Island & Sandesh Khali, 1827 Digha*3 20. Marphysa mosambica (Peters, 1854) Sagar Island, Jhingakhali, Gona, Parseymari, Mahanadi estuary3,11 21. Marphysa gravelyl Southern, 1921 Chilika lake1,10 22. Marphysa aenea (Blanchard in Gay, 1849) West Bengal1 23. Marphysa macintoshi Crossland, 1903 West Bengal1 24. Lycidice natalensis Kingberg, 1865 Sagar Island8 25. Eunice aphroditois (Pallas, 1788) Sagar Island3 26. Eunice laticeps Ehlers, 1868 Puri5 27. Lumbriconereis simplex (Southern, 1921) Chilka lake1,3 28. ONUPHIDAE Kinberg, Hyalinoecia tubicola (O.F. Müller, 1776) Sundarban6 1865 29. Dipopatra cuprea (Bosc, 1802) Sagar Island, Bakkhali, Canning, Bhngatushkhali, Chandipur2,3 30. Amphictene auricoma (O.F. Müller, 1776) Chandipur, Puri, Odisha coast5,8,12 31. Amphictene auricoma (O.F. Müller, 1776) Chilka Lake10 32. Onuphis eremita Audouin and Milne Puri, Konarak, Chilka lake2,5,8,12 Edwards, 1833 33. SCALIBREGMATIDAE Hyboscolex longiseta Schmarda, 1861 Sundarban6 Malmgren, 1867 (contd.) BALAKRISHNAN & TUDU: AN UPDATED CHECKLIST OF POLYCHAETES iii Table S1 — An updated checklist of polychaetes from Odisha and West Bengal coasts (contd.) S. No. Order Family Species Location 34. LUMBRINERIDAE Lumbrineris albidentata Ehlers, 1908 Sundarban6 Schmarda, 1861 35. Lumbrinereis bilabiata Misra, 1999 Sagar Island, Kakdweep, Bakhkhali3 36. Lumbrinereis polydesma Southern, 1921 Sagar Island, Kakdweep, Canning, Jhingakhali, Chilka lake1,3 37. Lumbrineris simplex (Southern, 1921) Chilka Lake7 38. Kuwaita heteropoda (Marenzeller, 1879) Bhangatushkhali3 39. Ninoenoto cirrata (Fauvel, 1932) Sagar Island, Canning, Sandeshkhali3,8 40. Scoletoma impatiens (Claparède, 1868) Ganjam coast, Puri5,8 41. MAGELONIDAE Magelona cincta Ehlers, 1908 Sundarban6 Cunningham & Ramage, 1888 42. MALDANIDAE Maldane sarsi Malmgren, 1865 Sundarban6 Malmgren, 1867 43. Sabaco gangeticus (Fauvel, 1932) Sandhead, Hooghly river mouth, West Bengal3,8 44. Euclymene annandalei (Southern, 1921) Chilika lake, Talsari*10 45. PHYLLODOCIDA POLYNOIDAE Lepidonotus squamatus (Linnaeus, 1758) Digha* Kinberg, 1856 46. Lepidonotus tenuisetosus (Gravier, 1901) Digha coast, Sagar Island, Bakkhali, Jhingakhali, Gona, Port Canning, off Puri, Odisha1,3 47. Lepidonotus jacksoni Kinberg, 1855 Ganjam coast, Odisha8 48. Augenerilepidonotus dictyolepis (Haswell, Puri, Odisha coast13 1883) 49. Gattyana fauveli Misra, 1999 Sagar Island3 50. Gaudichaudius cimex (Quatrefages, 1866) Sagar Island, Bakkhali, Balasore, Odisha1,3 51. Harmothoe dictyophora (Grube, 1878) Odisha1 52. GLYCERIDAE Glycera tridactyla Schmarda, 1861 Jambu Island, Sagar Island, Grube, 1850 Digha*3 53. Glycera lancadivae Schmarda, 1861 Sagar Island, Gopalpur, Puri, Chandipur, Konarak Sea2,3 54. Glycera rouxii Audouin & Milne Edwadrs, Sagar Island, Canning, 1833 Chandipore, Talsari*, Odisha1,3 55. Glycera tesselata Grube, 1863 Sundarbans, off Puri, Gopalpur, Chandipur Odisha1,2 56. Glycera benguellana Augener, 1931 Sundarban6 57. Glycera longipinnis Grube, 1878 Sundarban6 58. Glycera unicornis Lamarck, 1818 Chandipur, Sundarban2,6 59. Glycera alba (Southern, 1921) Chilika lake11 60. NEREIDIDAE Dendronereides gangetica Misra, 1999 Hooly estuary, Sagar Island, Blainville, 1818 Jhingakhali3,9,13-18 61. Dendronereis arborifera Peters, 1854 Sundarban, Bitarkonika estuary, Chandipur coast2 62. Lycastonereis indica Rao, 1981 Kakdweep, Bhushighta, Marichjhapi, Baitarani beach, Chandbali2,3,9,13,14,15,17,18,19 (contd.) iv INDIAN J GEO-MAR SCI, VOL 50, NO 06, JUNE 2021 Table S1 — An updated checklist of polychaetes from Odisha and West Bengal coasts (contd.) S. No. Order Family Species Location 63. Namalycastis fauveli Rao, 1981 Sagar Island, Sundarban, Kakdweep, Bhushighata, Marichjhapi, Haripur, Baitarani beach, Chandbali, Chilika lake2,3,10 64. Neanthes meggitti (Monro, 1931) West Bengal8 65. Neanthes reducta (Southern, 1921) Chilika lake7,10 66. Neanthes chilkensis Southern, 1921 Chilika lake, Barkud Island, Kaligai Island1,2,10 67. Neanthes chingrighattensis (Fauvel, 1932) Sagar Island, Kakdwip, Kolkata, West Bengal, Chandipur2,3,9 68. Neanthes arenaceodentata (Moore, 1903) Hughly, Kolkata1 69. Neanthes indica Kinberg, 1966 Mahanadi estuary, Gopalpur2 70. Neanthes operata Stimpson, 1856 Mahanadi estuary2 71. Neanthes willeyi (Day, 1934) Puri, Odisha2 72. Neanthes glandicincta (Southern, 1921) Birajmonichar, Gosaba, Chilika lake, Salt lake, Calcutta, Mahanadi estuary1,2,3,9,10,13- 19 73. Alitta succinea (Leuckart, 1847) Mahanadi estuary2 74. Nereis persica Fauvel, 1911 Gopalpur, Chandipur2 75. Namalycastis indica (Southern, 1921) Sagar Island, Kakdweep, Bakkhali, Bhushighata, Chilka lake, Bhasra Island, Kespur beach2,3,10 76. Dendronereides aestuarina Southern, 1921 Sagar Island, Namkhana, Sandeshkhali, Jhingakhali3,9,13-19 77. Dendronereides heteropoda Southern, 1921 Kakdwip, Bakkhali, Bhusighta, Kolkata, Chandipur beach, Burhabalang beach1,2,3,9,13-15,17-19 78. Dendronereides dayi Misra, 1999 Kakdwip, Bakkhali, Canning, Bhangatushkhali3,9,13-19 79. Ganganereis sootai Misra, 1999 Sagar Island, Jhingakhali, Jharkhali3,9,13-19 80. Leonates persica Wesenberg-Lund, 1949 Bhitarkonika estuary2 81. Perinereis cavifrons (Ehlers, 1920) Kakdwip3 82. Perinereis nigropunctata (Horst, 1889) Sundarbans , Kolkata, Sagar Island, Canning, Jhingakhali, Chilka lake, Mahanadi estuary, Gopalpur1,2,3,10,27 83. Perinereis nuntia (Lamarck, 1818) Odisha coast28 84. Perinereis falsovariegata Monro, 1933 Sundarban6 85. Perinereis aibuhitensis Grube, 1878 Mahanadi estuary2 86. Perinereis cultrifera (Grube, 1840) Mahanadi estuary, Gopalpur2 87. Perinereis vancaurica (Ehlers, 1868) Mahanadi estuary2 88. Platynereis dumerilii (Audouin & Milne Sundarban1,6 Edwards, 1833) 89. Pseudonereis varigata (Grube, 1857) Gopalpur2 90. Tylonereis bogoyawlenskyi Fauvel, 1911 Chandipur2 91. Tylonereis fauveli Southern, 1921 Mahanadi estuary2 92. Hediste diversicolor (O.F. Müller, 1776) Sundarban6 93. PHYLLODO Phyllodoce madeirensis Langerhans, 1880 Canning, Kakdweep, Jhingakhali, CIDAE Parseymari Odisha coast3,9,20,21 Örsted, 1843 (contd.) BALAKRISHNAN & TUDU: AN UPDATED CHECKLIST OF POLYCHAETES v Table S1 — An updated checklist of polychaetes from Odisha and West Bengal coasts (contd.) S. No. Order Family Species Location 94. Hypereteone barantollae (Fauvel, 1932) Bhitorkanika estuary, Sagar Island, Salt- Water lake, Kolkata, Odisha coast1,3 95. Eteone flava (Fabricius, 1780) Odisha coast12 96. Eulalia viridis (Linnaeus, 1767) Chilika lake10 97. Eumida sanguinea (Örsted, 1843) Chilika lake10 98. Eteonides elongate (Southern, 1914) Puri, Odisha coast5,22 99. SABELLARIIDAE Sabellaria pectinata Fauvel, 1932 Ganges Delta23 Johnston, 1865 100. SABELLARIIDAE Sabellaria pectinata intermedia Fauvel, 1932 Kakdwip & Namkhana3 101. Sabellaria alcocki Gravier, 1906 Matla river3 102. Sabellaria intoshi Fauvel, 1914 Sundarban6 103. SIGALIONIDAE Pisione complexa (Alikuhni, 1942) Puri and Konarak coast, Odisha5,22,24 104. Pisione gopalai (Alikuhni, 1941) Odisha coast24 105. Pisionidens indica (Aiyar & Alikunhi, 1940) Odisha coast25 106. SYLLIDAE Autolytus orientalis Willey, 1905 Chandipur2 Grube, 1850 107. Exogone heterosetosa McIntosh, 1885 Sundarban6 108. Syllis gracilis Grube, 1840 Sundarban6 109. Syllis benguellana Day, 1963 Sundarban6 110. Neopetitia amphophthalma (Siewing, 1956) Puri and Konarak coast2 111. Sphaerosyllis bengalensis Rao & Ganapati, Konarak coast2 1966 112. GONIADIDAE Goniada emerita Audouin & H. Milne Edwards, Haldi, Jharkhali, Sagar Island & Kinberg, 1866
Recommended publications
  • Polychaetes Associated with a Tropical Ocean Outfall: Synthesis of a Biomonitoring Program Off O'ahu, Hawai'f
    Polychaetes Associated with a Tropical Ocean Outfall: Synthesis ofa Biomonitoring Program off O'ahu, Hawai'F J. H. Bailey-Brock,2,3,4,5 B. Paavo,3,4 B. M. Barrett,3,4 and J. Dreyer3,4 Abstract: A comparison of benthic polychaete communities off the Sand Island Wastewater Outfall was undertaken to recognize organic enrichment indicator species for Hawaiian waters. Primary-treatment sewage is discharged off the south shore of O'ahu at 70 m depth. A historical data set spanning 9 yr for seven sites at 70 m and two recent studies at 20, 50, and 100 m depths were analyzed. Geochemical data did not support the assumption that the outfall is an im­ portant source of organic enrichment in nutrient-poor sandy sediments within oligotrophic tropical waters. Five polychaete species, however, appeared partic­ ularly sensitive, positively or negatively, to environmental conditions near the outfall. Neanthes arenaceodentata (Nereididae) and Ophryotrocha adherens (Dor­ villeidae) have been dominant at sites within the outfall's zone of initial dilution (ZID). Since 1993, N arenaceodentata has virtually disappeared, and 0. adherens concurrently became abundant and continued to flourish at ZID sites. Well­ known indicators within the Capitella capitata complex (Capitellidae) were pres­ ent at ZID and control (far field) sites though their ZID abundance was greater. Two sabellids, Euchone sp. Band Augeneriella dubia were inversely distributed, the smaller Euchone sp. B at far field sites and larger A. dubia within ZID sta­ tions. The former was most likely restricted to a greater proportion offine sed­ iment particles at two far field sites.
    [Show full text]
  • The 17Th International Colloquium on Amphipoda
    Biodiversity Journal, 2017, 8 (2): 391–394 MONOGRAPH The 17th International Colloquium on Amphipoda Sabrina Lo Brutto1,2,*, Eugenia Schimmenti1 & Davide Iaciofano1 1Dept. STEBICEF, Section of Animal Biology, via Archirafi 18, Palermo, University of Palermo, Italy 2Museum of Zoology “Doderlein”, SIMUA, via Archirafi 16, University of Palermo, Italy *Corresponding author, email: [email protected] th th ABSTRACT The 17 International Colloquium on Amphipoda (17 ICA) has been organized by the University of Palermo (Sicily, Italy), and took place in Trapani, 4-7 September 2017. All the contributions have been published in the present monograph and include a wide range of topics. KEY WORDS International Colloquium on Amphipoda; ICA; Amphipoda. Received 30.04.2017; accepted 31.05.2017; printed 30.06.2017 Proceedings of the 17th International Colloquium on Amphipoda (17th ICA), September 4th-7th 2017, Trapani (Italy) The first International Colloquium on Amphi- Poland, Turkey, Norway, Brazil and Canada within poda was held in Verona in 1969, as a simple meet- the Scientific Committee: ing of specialists interested in the Systematics of Sabrina Lo Brutto (Coordinator) - University of Gammarus and Niphargus. Palermo, Italy Now, after 48 years, the Colloquium reached the Elvira De Matthaeis - University La Sapienza, 17th edition, held at the “Polo Territoriale della Italy Provincia di Trapani”, a site of the University of Felicita Scapini - University of Firenze, Italy Palermo, in Italy; and for the second time in Sicily Alberto Ugolini - University of Firenze, Italy (Lo Brutto et al., 2013). Maria Beatrice Scipione - Stazione Zoologica The Organizing and Scientific Committees were Anton Dohrn, Italy composed by people from different countries.
    [Show full text]
  • Ecotoxicology of Estuarine Amphipod Paracorophium Excavatum
    E icolo fEstua ·ne Amphipod Paracorophium excavatum A thesis Submitted in partial fulfilment the requirements for Degree of Master of Science in Environmental Science at The University of Canterbury by Carol Wong Hee Ting University of Canterbury 1999 ABSTRACT The estuarine tube dwelling amphipod Paracorophium excavatum was investigated for its suitability as a bio-indicator and bio-monitor. Distribution patterns of P. excavatum were determined at 13 sites in the Canterbury region that differed in particle size distribution ranging from sandy to muddy sediment, with overall10w organic content. Low tide salinity ranged from 5 to 33 0/00 between sites and sediment moisture content ranged between 23 to 41 % moisture. Amphipods were absent from most sites within the Avon-Heathcote Estuary. The availability, life history and fecundity of P. excavatum were compared from intertidal mudflat sites in Brooklands Lagoon and Kairaki over a period of thirteen months. Four sediment core samples were collected at monthly intervals and P. excavatum IS population structure and life history pattern studied. The life history til· <: of P. excavatum can be characterised bY fast-growing, annual, iteroporous, bivoltine, females ovigerous throughout the year and thelygenous (female biased) population. P. excavatum showed relative consistency in abundance throughout the year with monthly densities ranging from 875.79 per 0.1 m-2 (July) to 1754.77 per 0.1 m-2 (December) at Brooklands Lagoon and 1031.83 per 0.1 m2 (November) to 1780.24 per 0.1 m2 (December) at Kairaki. There was a linear relationship between numbers of eggs per female and female length.
    [Show full text]
  • SCAMIT Newsletter Vol. 22 No. 6 2003 October
    October, 2003 SCAMIT Newsletter Vol. 22, No. 6 SUBJECT: B’03 Polychaetes continued - Polycirrus spp, Magelonidae, Lumbrineridae, and Glycera americana/ G. pacifica/G. nana. GUEST SPEAKER: none DATE: 12 Jaunuary 2004 TIME: 9:30 a.m. to 3:30 p. m. LOCATION: LACMNH - Worm Lab SWITCHED AT BIRTH The reader may notice that although this is only the October newsletter, the minutes from the November meeting are included. This is not proof positive that time travel is possible, but reflects the mysterious translocation of minutes from the September meeting to a foster home in Detroit. Since the November minutes were typed and ready to go, rather than delay yet another newsletter during this time of frantic “catching up”, your secretary made the decision to go with what was available. Let me assure everyone that the September minutes will be included in next month’s newsletter. Megan Lilly (CSD) NOVEMBER MINUTES The October SCAMIT meeting on Piromis sp A fide Harris 1985 miscellaneous polychaete issues was cancelled Anterior dorsal view. Image by R. Rowe due to the wildfire situation in Southern City of San Diego California. It has been rescheduled for January ITP Regional 2701 rep. 1, 24July00, depth 264 ft. The SCAMIT Newsletter is not deemed to be a valid publication for formal taxonomic purposes. October, 2003 SCAMIT Newsletter Vol. 22, No. 6 12th. The scheduled topics remain: 1) made to accommodate all expected Polycirrus spp, 2) Magelonidae, 3) participants. If you don’t have his contact Lumbrineridae, and 4) Glycera americana/G. information, RSVP to Secretary Megan Lilly at pacifica/G.
    [Show full text]
  • Expression of Distal-Less, Dachshund, and Optomotor Blind in Neanthes Arenaceodentata
    Dev Genes Evol (2010) 220:275–295 DOI 10.1007/s00427-010-0346-0 ORIGINAL ARTICLE Expression of Distal-less, dachshund, and optomotor blind in Neanthes arenaceodentata (Annelida, Nereididae) does not support homology of appendage-forming mechanisms across the Bilateria Christopher J. Winchell & Jonathan E. Valencia & David K. Jacobs Received: 26 July 2010 /Accepted: 9 November 2010 /Published online: 30 November 2010 # The Author(s) 2010. This article is published with open access at Springerlink.com Abstract The similarity in the genetic regulation of mesoderm. Domains of omb expression include the brain, arthropod and vertebrate appendage formation has been nerve cord ganglia, one pair of anterior cirri, presumed interpreted as the product of a plesiomorphic gene precursors of dorsal musculature, and the same pharyngeal network that was primitively involved in bilaterian ganglia and presumed interneurons that express dac. appendage development and co-opted to build appen- Contrary to their roles in outgrowing arthropod and dages (in modern phyla) that are not historically related vertebrate appendages, Dll, dac,andomb lack comparable as structures. Data from lophotrochozoans are needed to expression in Neanthes appendages, implying independent clarify the pervasiveness of plesiomorphic appendage- evolution of annelid appendage development. We infer forming mechanisms. We assayed the expression of three that parapodia and arthropodia are not structurally or arthropod and vertebrate limb gene orthologs, Distal-less mechanistically homologous (but their primordia might (Dll), dachshund (dac), and optomotor blind (omb), in be), that Dll’s ancestral bilaterian function was in sensory direct-developing juveniles of the polychaete Neanthes and central nervous system differentiation, and that arenaceodentata.
    [Show full text]
  • Variation and Ontogenetic Changes of Opercular Paleae in a Population Of
    SCIENTIA MARINA 79(1) March 2015, 137-150, Barcelona (Spain) ISSN-L: 0214-8358 doi: http://dx.doi.org/10.3989/scimar.04127.19A Variation and ontogenetic changes of opercular paleae in a population of Sabellaria spinulosa (Polychaeta: Sabellaridae) from the South Adriatic Sea, with remarks on larval development Marco Lezzi 1, Frine Cardone 2, Barbara Mikac 3, Adriana Giangrande 1 1 DiSTeBA University of Salento, CoNISMa, Via Provinciale Lecce- Monteroni, 73100 Lecce, Italy. E-mail: [email protected] 2 Department of Zoology, Via Orabona 4, 70125 University of Bari, Italy. 3 Center for Marine Research, Ruđer Boković Institute, Giordano Paliaga 5, 52210 Rovinj, Croatia. Summary: Sabellaria alcocki Gravier, 1906, described for the Indian Ocean, should not be present in the Mediterranean area. Though S. spinulosa alcocki, a Mediterranean variety, can be well-distinguished from S. alcocki, it has recently been referred to as S. alcocki. Thus, S. alcocki appears in the Italian coast checklist. The recent finding of S. spinulosa reefs along the southern Adriatic coast, the first report of these biogenic constructions in the Mediterranean area, allowed us to compare its morphological variability with that of S. alcocki. A morphometric analysis of the opercular paleae showed a great deal of intrapopulation, size-independent variation, which cannot justify the existence of varieties within S. spinulosa. Moreover, the analysis of post-settlement development showed that opercular features change during individual growth. Recently set- tled individuals resemble S. alcocki, while the more advanced life stages become closer to S. spinulosa. Accordingly, we hypothesize that part of the erroneous Mediterranean records of S.
    [Show full text]
  • (Polychaeta, Polynoidae), in the White Sea
    Invertebrate Zoology, 1(1): 6573 © INVERTEBRATE ZOOLOGY, 2004 Population ecology of two simpatric polychaetes, Lepidonotus squamatus and Harmothoe imbricata (Polychaeta, Polynoidae), in the White Sea Maria Plyuscheva1, Daniel Martin2, Temir Britayev1 1A. N. Severtzov Institute of Ecology and Evolution, Russian Academy of Sciences, Leninsky pr. 33, Moscow 117071, Russia. e-mail: [email protected] 2Centre dEstudis Avançats de Blanes (CSIC), carrer daccés a la Cala Sant Francesc 14, 17300 Blanes (Girona), Catalunya (Spain). e-mail: [email protected] ABSTRACT: Under the critical environmental conditions of the White Sea, Lepidonotus squamatus and Harmothoe imbricata coexist in the same habitat, often showing recurrent alternations in dominance. L. squamatus is a long-living, slow growing broadcast spawner, while H. imbricata is a short-living and quick growing species, with complex reproductive behaviour. These different life strategies may allow them to respond in a different way to the environmental limitations of the study site, this likely being the most appropriate explanation to the observed alternation in dominance. KEYWORDS: Population dynamics; growth; scale-worms; the White Sea. Ýêîëîãèÿ ïîïóëÿöèé äâóõ ñèìïàòðè÷åñêèõ âèäîâ ïîëèõåò Lepidonotus squamatus è Harmothoe imbricata (Polychaeta, Polynoidae) â Áåëîì ìîðå Ì. Â. Ïëþùåâà1, Ä. Ìàðòèí2, Ò. À. Áðèòàåâ1 1Èíñòèòóò ïðîáëåì ýêîëîãèè è ýâîëþöèè èì. À.Í. Ñåâåðöîâà, Ðîññèéñêàÿ Àêàäåìèÿ Íàóê, Ëåíèíñêèé ïð. 33, Ìîñêâà, 117071, Ðîññèÿ. e-mail: [email protected] 2Centre dEstudis Avançats de Blanes (CSIC), carrer daccés a la Cala Sant Francesc 14, 17300 Blanes (Girona), Catalunya (Spain). e-mail: [email protected] ÐÅÇÞÌÅ:  ýêñòðåìàëüíûõ óñëîâèÿõ Áåëîãî ìîðÿ,Lepidonotus squamatus è Harmothoe imbricata çàíèìàþò ñõîäíûå ýêîëîãè÷åñêèå íèøè, äåìîíñòðèðóÿ ïåðèîäè÷åñêîå ÷åðåäîâàíèå â äîìèíèðîâàíèè.
    [Show full text]
  • The Namanereidinae (Polychaeta: Nereididae). Part 1, Taxonomy and Phylogeny
    © Copyright Australian Museum, 1999 Records of the Australian Museum, Supplement 25 (1999). ISBN 0-7313-8856-9 The Namanereidinae (Polychaeta: Nereididae). Part 1, Taxonomy and Phylogeny CHRISTOPHER J. GLASBY National Institute for Water & Atmospheric Research, PO Box 14-901, Kilbirnie, Wellington, New Zealand [email protected] ABSTRACT. A cladistic analysis and taxonomic revision of the Namanereidinae (Nereididae: Polychaeta) is presented. The cladistic analysis utilising 39 morphological characters (76 apomorphic states) yielded 10,000 minimal-length trees and a highly unresolved Strict Consensus tree. However, monophyly of the Namanereidinae is supported and two clades are identified: Namalycastis containing 18 species and Namanereis containing 15 species. The monospecific genus Lycastoides, represented by L. alticola Johnson, is too poorly known to be included in the analysis. Classification of the subfamily is modified to reflect the phylogeny. Thus, Namalycastis includes large-bodied species having four pairs of tentacular cirri; autapomorphies include the presence of short, subconical antennae and enlarged, flattened and leaf-like posterior cirrophores. Namanereis includes smaller-bodied species having three or four pairs of tentacular cirri; autapomorphies include the absence of dorsal cirrophores, absence of notosetae and a tripartite pygidium. Cryptonereis Gibbs, Lycastella Feuerborn, Lycastilla Solís-Weiss & Espinasa and Lycastopsis Augener become junior synonyms of Namanereis. Thirty-six species are described, including seven new species of Namalycastis (N. arista n.sp., N. borealis n.sp., N. elobeyensis n.sp., N. intermedia n.sp., N. macroplatis n.sp., N. multiseta n.sp., N. nicoleae n.sp.), four new species of Namanereis (N. minuta n.sp., N. serratis n.sp., N. stocki n.sp., N.
    [Show full text]
  • (Annelida) Species in the Mediterranean Sea Dna-Barcoding Per La Corretta Identificazione Delle Specie Del Genere Sabellaria (Annelida) in Mediterraneo
    Biol. Mar. Mediterr. (2015), 22 (1): 109-110 E. SCHImmENTI, S. LO BRUTTO, F. BADALAMENTI1, A. GIANGRANDE2, B. MIKAC1, L. MUSCO1 Dipartimento STeBiCeF, Sezione di Biologia Animale, Università di Palermo, Via Archirafi, 18 - 90123 Palermo, Italia. [email protected] 1CNR-IAMC, Castellammare del Golfo (TP), Italia. 2DiSTeBA, Università del Salento, Lecce, Italia. DNA-BARCODING TO SOLVE THE TRICKY CASE OF CO-OCCURRING SABELLARIA (ANNELIDA) SPECIES IN THE MEDITERRANEAN SEA DNA-BARCODING PER LA CORRETTA IDENTIFICAZIONE DELLE SPECIE DEL GENERE SABELLARIA (ANNELIDA) IN MEDITERRANEO Abstract - Intraspecific morphological variation of key taxonomic features is probably responsible for frequent misidentification of Sabellaria (Lamarck, 1818) species. This is the case of Sabellaria alcocki Gravier, 1906 whose Mediterranean records probably refer to juveniles of S. spinulosa (Leuckart, 1849). We hereby provide molecular tools (DNA barcoding) to improve correct delimitation of the Mediterranean species of this genus. Key-words: Polychaeta, Sabellaria alveolata, Sabellaria spinulosa, Sabellaria alcocki, COI. Introduction - Sabellaria (Lamarck, 1818) species are gregarious tube-builder polychaetes which produce complex reefs representing valuable and diverse habitats in coastal areas (La Porta and Nicoletti, 2009). Today three Sabellaria species are recorded for the Mediterranean Sea: S. alveolata (L., 1767), S. spinulosa (Leuckart, 1849) and S. alcocki Gravier, 1906 (Castelli et al., 2008). This last is a valid species but according to several authors it is exclusive of the Indian Ocean and its Mediterranean records should be carefully revised (Lezzi et al., 2015). The operculum is of paramount taxonomic importance for Sabellaria species identification, but its intraspecific variation, especially during development, may lead to confusion. This is the case of S.
    [Show full text]
  • SPECIAL PUBLICATION 6 the Effects of Marine Debris Caused by the Great Japan Tsunami of 2011
    PICES SPECIAL PUBLICATION 6 The Effects of Marine Debris Caused by the Great Japan Tsunami of 2011 Editors: Cathryn Clarke Murray, Thomas W. Therriault, Hideaki Maki, and Nancy Wallace Authors: Stephen Ambagis, Rebecca Barnard, Alexander Bychkov, Deborah A. Carlton, James T. Carlton, Miguel Castrence, Andrew Chang, John W. Chapman, Anne Chung, Kristine Davidson, Ruth DiMaria, Jonathan B. Geller, Reva Gillman, Jan Hafner, Gayle I. Hansen, Takeaki Hanyuda, Stacey Havard, Hirofumi Hinata, Vanessa Hodes, Atsuhiko Isobe, Shin’ichiro Kako, Masafumi Kamachi, Tomoya Kataoka, Hisatsugu Kato, Hiroshi Kawai, Erica Keppel, Kristen Larson, Lauran Liggan, Sandra Lindstrom, Sherry Lippiatt, Katrina Lohan, Amy MacFadyen, Hideaki Maki, Michelle Marraffini, Nikolai Maximenko, Megan I. McCuller, Amber Meadows, Jessica A. Miller, Kirsten Moy, Cathryn Clarke Murray, Brian Neilson, Jocelyn C. Nelson, Katherine Newcomer, Michio Otani, Gregory M. Ruiz, Danielle Scriven, Brian P. Steves, Thomas W. Therriault, Brianna Tracy, Nancy C. Treneman, Nancy Wallace, and Taichi Yonezawa. Technical Editor: Rosalie Rutka Please cite this publication as: The views expressed in this volume are those of the participating scientists. Contributions were edited for Clarke Murray, C., Therriault, T.W., Maki, H., and Wallace, N. brevity, relevance, language, and style and any errors that [Eds.] 2019. The Effects of Marine Debris Caused by the were introduced were done so inadvertently. Great Japan Tsunami of 2011, PICES Special Publication 6, 278 pp. Published by: Project Designer: North Pacific Marine Science Organization (PICES) Lori Waters, Waters Biomedical Communications c/o Institute of Ocean Sciences Victoria, BC, Canada P.O. Box 6000, Sidney, BC, Canada V8L 4B2 Feedback: www.pices.int Comments on this volume are welcome and can be sent This publication is based on a report submitted to the via email to: [email protected] Ministry of the Environment, Government of Japan, in June 2017.
    [Show full text]
  • Appendix 5F – San Diego County Municipal Copermittees Sediment Monitoring Plan
    Appendix 5F – San Diego County Municipal Copermittees Sediment Monitoring Plan San Diego County Municipal Copermittees Sediment Monitoring Plan-Final Prepared For: County of San Diego Municipal Copermittees November 2014 San Diego County Municipal Copermittees Sediment Monitoring Plan-Final Prepared For: County of San Diego Municipal Copermittees Prepared By: Weston Solutions, Inc. 5817 Dryden Place, Suite 101 Carlsbad, California 92008 November 2014 San Diego County Municipal Copermittees Sediment Monitoring Plan-Final November 2014 TABLE OF CONTENTS 1.0 INTRODUCTION .............................................................................................................. 1 1.1 Background ............................................................................................................. 1 1.2 Monitoring Objective .............................................................................................. 2 2.0 MATERIALS AND METHODS ........................................................................................ 3 2.1 Field Collection Program ........................................................................................ 3 Station Selection .......................................................................................... 3 Permitting .................................................................................................... 4 Monitoring Season and Frequency .............................................................. 4 Sampling Vessels .......................................................................................
    [Show full text]
  • Polychaeta Lana Crumrine
    Polychaeta Lana Crumrine Well over 200 species of the class Polychaeta are found in waters off the shores of the Pacific Northwest. Larval descriptions are not available for the majority of these species, though descriptions are available of the larvae for at least some species from most families. This chapter provides a dichotomous key to the polychaete larvae to the family level for those families with known or suspected pelagic larva. Descriptions have be $in gleaned from the literature from sites worldwide, and the keys are based on the assumption that developmental patterns are similar in different geographical locations. This is a large assumption; there are cases in which development varies with geography (e.g., Levin, 1984). Identifying polychaetes at the trochophore stage can be difficult, and culturing larvae to advanced stages is advised by several experts in the field (Bhaud and Cazaux, 1987; Plate and Husemann, 1994). Reproduction, Development, and Morphology Within the polychaetes, the patterns of reproduction and larval development are quite variable. Sexes are separate in most species, though hermaphroditism is not uncommon. Some groups undergo a process called epitoky at sexual maturation; benthic adults develop swimming structures, internal organs degenerate, and mating occurs between adults swimming in the water column. Descriptions of reproductive pattern, gamete formation, and spawning can be found in Strathmann (1987). Larval polychaetes generally develop through three stages: the trochophore, metatrochophore, and nectochaete stages. Trochophores are ciliated larvae (see Fig. 1).A band of cilia, the prototroch, is used for locomotion and sometimes feeding. Trochophore larvae are generally broad anteriorly and taper posteriorly.
    [Show full text]