View Gallery Sheet

Total Page:16

File Type:pdf, Size:1020Kb

View Gallery Sheet 34 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 68 70 71 72 73 74 75 78 79 Nudibranchia 66 67 69 76 77 80 81 82 84 83 85 86 87 88 89 90 91 92 93 94 95 Butterflies of the Sea 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 Isabella Kirkland 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 Nudibranchia is a celebration of the wild variety of physical 134 136 137 138 139 142 and behavioral traits that have evolved in this order of animals. 135 140 141 143 Nudibranchs are mollusks without shells: “nudi” = naked and 144 146 “branch” = gill. The 206 species here are just a small portion 145 147 148 149 150 151 152 153 of those known: estimates of the total number of species run from 3,000 to 6,000. Given how vast the oceans are, how short 154 155 156 157 161 a time we humans have been able to physically explore under- 158 159 160 162 water, and how small a percentage of the 7/10’s of Earth’s total area has been visited, who knows? The oceans are the last 163 164 165 166 167 169 170 171 great frontier on the planet. Nudibranchs inhabit every part of 168 every ocean: from shallow reefs and mudflats to the depth of a thermal vent, from the Arctic to the equator. These creatures 172 175 173 174 176 177 178 are short lived. Many have only a few days to a few months to 179 reproduce once they reach sexual maturity. In order to maximize their chances of finding each other, all are hermaphrodites. They 181 183 can also mate across generations, in what is called protandry 180 182 184 185 186 (making a baby with your grandfather or great niece): any sexually mature nudibranch can mate with any other mature one of its species, regardless of size. Penile and vaginal structural 187 188 192 variation in nudibranchs is truly stupefying and wondrous. 189 190 191 A wide array of mimicries and camouflages has also evolved among nudibranchs. Some slugs’ cerata look so much like their prey species that the slugs are virtually invisible if nestled amongst them. Many can swim. 193 194 195 196 197 Nudibranchia, 2014 Oil & alkyd on canvas over panel, 4' x 5' Animals are painted to scale. For greater visibility, they are 202 198 199 200 201 represented at the maximum end of their size range. A new series of paintings 204 205 Aquae 203 206 2014 www.IsabellaKirkland.com species List 51 Chromodoris striatella 1877 103 Goniobranchus geminus 1987 155 Scyllaea pelagica 1758 52 Polycera abei 1960 104 Felimare acriba 1967 156 Armina Californica 1863 1 Okenia cochimi 2004 53 Felimida punctilucens 1890 105 Ardeadoris rubroannulata 1986 157 Nembrotha yonowae 1992 Nudibranchia 2 Doto amyra 1961 54 Felimida sphoni​​ 1971 106 Dendrodoris krusensternii 1850 158 Lomanotus genei​​ 1846 3 Aegires pruvotfolae 2004 55 Hypselodoris babai 2000 107 Atagema alba 1927 159 Gymnodoris aurita 1852 4 Eubranchus mandapamensis 1968 Butterflies of the Sea 56 Cerberilla albopunctata 1976 108 Goniobranchus geometricus 1928 160 Nembrotha cristata 1877 5 Dermatobranchus albineus 2011 57 Phyllodesmium poindimiei​​ 1928 109 Hypselodoris paulinae 1999 161 Baeolidia moebii 1888 6 Gymnodoris nigricolor 1960 58 Phestilla lugubris 1870 110 Dendrodoris krebsii 1863 162 Phyllidia varicosa 1801 Isabella Kirkland 7 Eubranchus inabai 1964 59 Roboastra arika 1967 111 Discodoris boholiensis 1877 163 Miamira moloch 1988 8 Babakina indopacifica 2007 60 Plocamopherus lucayensis​​ 1988 112 Cerberilla affinis 1888 164 Nembrotha kubaryana 1877 9 Noumea laboutei 1986 61 Goniobranchus fidelis 1858 113 Marionia elongoreticulata 2007 165 Halgerda okinawa 2000 10 Phyllodesmium macphersonae 1962 62 Dirona picta 1905 114 Miamira sinuatum 1824 166 Phyllidiopsis shireenae 1990 11 Cadlinella ornatissima 1928 63 Ceratophyllidia africana​​ 1903 115 Reticulidia halgerda 1990 167 Hypselodoris pulchella 1830 12 Hypselodoris alboterminata 1999 64 Hypselodoris nigrostriata 1904 116 Spurilla neapolitana 1841 168 Glossodoris hikuerensis 1954 13 Trapania miltabrancha 2008 65 1961 117 1877 169 1984 special thanks to: Polycera chilluna Tambja morosa Ardeadoris egretta 14 Halgerda albocristata 1998 66 Herviella mietta 1965 118 Hermissenda crassicornis​​ 1831 170 Felimare zebra 1889 15 Noumea romeri 1928 To all of you who shot and shared photos 67 Glaucus atlanticus 1777 119 Felimare ghiselini 1978 171 Ceratosoma tenue 1876 16 Facelina rhodopos 2000 of nudibranchs on the web: thank you for helping me 68 Notobryon wardi 1936 120 Tritoniella belli 1907 172 Dendrodoris warta 1976 17 Jorunna parva 1938 see them clearly through your collective lens. 69 Taringa halgerda 1998 121 Dermatobranchus ornatus 1874 173 Gymnodoris ceylonica 1858 18 Tambja oliva 1977 70 Sakuraeolis kirembosa 1980 122 Chromodoris kuiteri 1982 174 Dermatobranchus gonatophora 1824 19 Okenia rosacea 1905 71 1993 123 1804 175 1828 perpetual thanks to: Reticulidia fungia Phyllidia ocellata Marionia rubra 20 Trapania naeva 2008 72 Felimare fontandraui 1951 124 Halgerda willeyi 1904 176 Doriprismatica stellata 1986 21 Embletonia gracilis 1928 John McCosker 73 Phyllodesmium kabiranum​​ 1991 125 Nembrotha megalocera 1990 177 Tambja verconis 1905 22 Cerberilla chavezi 2007 Terry Gosliner 74 Noumea verconis 1905 126 Flabellina japonica 1937 178 Kalinga ornata 1864 23 Phyllidiopsis sphingis 1993 The California Academy of Sciences 75 Pauleo jubatus 1992 127 Phyllidiopsis krempfi 1957 179 Felimare picta 1836 24 Ancula gibbosa 1818 Ryan Phelan and Stewart Brand 76 Chromodoris elisabethina​​ 1877 128 Plocamopherus imperialis 1864 180 Aegires minor 1904 25 Charcotia granulosa 1906 The Long Now Foundation 77 Tambja eliora 1967 129 Diaulula sandiegensis 1863 181 Doris montereyensis 1863 26 Cuthona caerulea 1804 Peter and Mimi Buckley 78 Dondice occidentalis 1925 130 Dendrodoris nigra 1855 182 Triopha catalinae 1863 27 Polycera odhneri 1955 Christopher Tellis 79 Tambja fantasmalis 1986 131 Nembrotha milleri 1997 183 Phyllodesmium longicirrum 1905 28 Thorunna arbuta​​ 1961 and Hudson 80 Flabellina trophina 1890 132 Felimare agassizii 1894 184 Armina variolosa 1904 29 Limacia cockerelli 1905 81 Phyllodesmium rudmani 2006 133 Doriopsilla spaldingi 1998 185 Bornella anguilla 1984 30 Acanthodoris rhodoceras​​ 1905 82 Janolus ignis 1986 134 Aegires serenae 1997 186 Dendrodoris albopurpura 1957 31 Flabellina hamanni 1994 83 Cuthona yamasui 1993 135 Miamira alleni 1996 187 Platydoris formosa 1864 32 Favorinus tsuruganus 1964 84 Halgerda tessellata 1880 136 Tritonia bollandi 2003 188 Pteraeolidia ianthina 1864 33 Anteaeolidiella indica 1888 85 Bornella stellifer 1848 137 Felimida baumanni 1970 189 Ceratosoma brevicaudatum 1876 34 Cumanotus beaumonti 1906 Blue Numbers indicate species found on 86 Goniobranchus roboi 1998 138 Felimare californiensis 1879 190 Triopha maculata 1905 35 Doto ussi 1982 the West Coast of the United States. 87 Doriprismatica tibboeli 2005 139 Melibe leonina 1852 191 Jorunna rubescens 1876 36 Acanthodoris hudsoni 1905 88 Tambja gratiosa 1890 140 Nembrotha rosannulata 2008 192 Dendrodoris tuberculosa 1832 37 Ceratophyllidia papilligera​​ 1890 Orange Numbers indicate date of discovery. 89 Flabellina cynara 1967 141 Hypselodoris tryoni 1873 193 Dirona albolineata 1905 38 Doto pinnatifida 1804 90 Polycera capensis 1824 142 Platydoris cruenta 1832 194 Dendrodoris rainfordi​​ 1932 39 Greilada elegans 1894 91 Janolus cristatus 1841 143 Nembrotha chamberlaini​​ 1997 195 Tambja gabrielae 2005 40 Crosslandia viridis 1902 92 Jason mirabilis 1974 144 Aeolidia papillosa 1761 196 Armina papillata 1933 41 Dermatobranchus rubidus​​ 1852 93 Gymnodoris striata 1908 145 Goniobranchus annulatus​​ 1904 197 Doris odhneri 1966 42 Flabellina exoptata 1991 94 Chromodoris magnifica 1832 146 Hypselodoris apolegma 2001 198 Doris wellingtonensis 1877 43 Mexichromis macropus 1983 95 Jorunna pardus​​ 1981 147 Aegires gardineri​​ 1906 199 Dendronotus iris 1863 A New Series of Paintings 44 Roboastra gracilis 1877 96 Hypselodoris bennetti 1864 148 Jorunna funebris 1859 200 Tochuina tetraquetra 1788 45 Lomanotus vermiformis 1908 97 Glossodoris cincta 1888 149 Flabellina iodinea 1863 201 Dendronotus rufus 1921 Aquae 46 Halgerda stricklandi 1999 98 Leminda millecra 1985 150 Miamira miamirana 1875 202 Asteronotus cespitosus 1824 47 Tambja stegosauriformis 2005 99 Dendrodoris guttata 1917 151 Goniobranchus collingwoodi 1987 203 Hexabranchus sanguineus 1830 2014 48 Cadlina sparsa 1921 100 Phyllidia coelestis 1905 152 Doriprismatica atromarginata 1804 204 Melibe viridis 1858 49 Chromodoris lochi 1982 101 Goniobranchus coi 1956 153 Bonisa nakaza 1981 205 Tochuina tetraquetra 1788 www.IsabellaKirkland.com 50 Phyllidiella rosans 1873 102 Gymnodoris impudica 1830 154 Tambja sagamiana 1955 206 Roboastra tigris 1978.
Recommended publications
  • Appendix to Taxonomic Revision of Leopold and Rudolf Blaschkas' Glass Models of Invertebrates 1888 Catalogue, with Correction
    http://www.natsca.org Journal of Natural Science Collections Title: Appendix to Taxonomic revision of Leopold and Rudolf Blaschkas’ Glass Models of Invertebrates 1888 Catalogue, with correction of authorities Author(s): Callaghan, E., Egger, B., Doyle, H., & E. G. Reynaud Source: Callaghan, E., Egger, B., Doyle, H., & E. G. Reynaud. (2020). Appendix to Taxonomic revision of Leopold and Rudolf Blaschkas’ Glass Models of Invertebrates 1888 Catalogue, with correction of authorities. Journal of Natural Science Collections, Volume 7, . URL: http://www.natsca.org/article/2587 NatSCA supports open access publication as part of its mission is to promote and support natural science collections. NatSCA uses the Creative Commons Attribution License (CCAL) http://creativecommons.org/licenses/by/2.5/ for all works we publish. Under CCAL authors retain ownership of the copyright for their article, but authors allow anyone to download, reuse, reprint, modify, distribute, and/or copy articles in NatSCA publications, so long as the original authors and source are cited. TABLE 3 – Callaghan et al. WARD AUTHORITY TAXONOMY ORIGINAL SPECIES NAME REVISED SPECIES NAME REVISED AUTHORITY N° (Ward Catalogue 1888) Coelenterata Anthozoa Alcyonaria 1 Alcyonium digitatum Linnaeus, 1758 2 Alcyonium palmatum Pallas, 1766 3 Alcyonium stellatum Milne-Edwards [?] Sarcophyton stellatum Kükenthal, 1910 4 Anthelia glauca Savigny Lamarck, 1816 5 Corallium rubrum Lamarck Linnaeus, 1758 6 Gorgonia verrucosa Pallas, 1766 [?] Eunicella verrucosa 7 Kophobelemon (Umbellularia) stelliferum
    [Show full text]
  • Sea Slugs – Divers' Favorites, Taxonomists' Problems
    Aquatic Science & Management, Vol. 1, No. 2, 100-110 (Oktober 2013) ISSN 2337-4403 Pascasarjana, Universitas Sam Ratulangi e-ISSN 2337-5000 http://ejournal.unsrat.ac.id/index.php/jasm/index jasm-pn00033 Sea slugs – divers’ favorites, taxonomists’ problems Siput laut – disukai para penyelam, masalah bagi para taksonom Kathe R. Jensen Zoological Museum (Natural History Museum of Denmark), Universitetsparken 15, DK-2100 Copenhagen Ø, Denmark E-mail: [email protected] Abstract: Sea slugs, or opisthobranch molluscs, are small, colorful, slow-moving, non-aggressive marine animals. This makes them highly photogenic and therefore favorites among divers. The highest diversity is found in tropical waters of the Indo-West Pacific region. Many illustrated guidebooks have been published, but a large proportion of species remain unidentified and possibly new to science. Lack of funding as well as expertise is characteristic for taxonomic research. Most taxonomists work in western countries whereas most biodiversity occurs in developing countries. Cladistic analysis and molecular studies have caused fundamental changes in opisthobranch classification as well as “instability” of scientific names. Collaboration between local and foreign scientists, amateurs and professionals, divers and academics can help discovering new species, but the success may be hampered by lack of funding as well as rigid regulations on collecting and exporting specimens for taxonomic research. Solutions to overcome these obstacles are presented. Keywords: mollusca; opisthobranchia; biodiversity; citizen science; taxonomic impediment Abstrak: Siput laut, atau moluska golongan opistobrancia, adalah hewan laut berukuran kecil, berwarna, bergerak lambat, dan tidak bersifat agresif. Alasan inilah yang membuat hewan ini sangat fotogenik dan menjadi favorit bagi para penyelam.
    [Show full text]
  • A Radical Solution: the Phylogeny of the Nudibranch Family Fionidae
    RESEARCH ARTICLE A Radical Solution: The Phylogeny of the Nudibranch Family Fionidae Kristen Cella1, Leila Carmona2*, Irina Ekimova3,4, Anton Chichvarkhin3,5, Dimitry Schepetov6, Terrence M. Gosliner1 1 Department of Invertebrate Zoology, California Academy of Sciences, San Francisco, California, United States of America, 2 Department of Marine Sciences, University of Gothenburg, Gothenburg, Sweden, 3 Far Eastern Federal University, Vladivostok, Russia, 4 Biological Faculty, Moscow State University, Moscow, Russia, 5 A.V. Zhirmunsky Instutute of Marine Biology, Russian Academy of Sciences, Vladivostok, Russia, 6 National Research University Higher School of Economics, Moscow, Russia a11111 * [email protected] Abstract Tergipedidae represents a diverse and successful group of aeolid nudibranchs, with approx- imately 200 species distributed throughout most marine ecosystems and spanning all bio- OPEN ACCESS geographical regions of the oceans. However, the systematics of this family remains poorly Citation: Cella K, Carmona L, Ekimova I, understood since no modern phylogenetic study has been undertaken to support any of the Chichvarkhin A, Schepetov D, Gosliner TM (2016) A Radical Solution: The Phylogeny of the proposed classifications. The present study is the first molecular phylogeny of Tergipedidae Nudibranch Family Fionidae. PLoS ONE 11(12): based on partial sequences of two mitochondrial (COI and 16S) genes and one nuclear e0167800. doi:10.1371/journal.pone.0167800 gene (H3). Maximum likelihood, maximum parsimony and Bayesian analysis were con- Editor: Geerat J. Vermeij, University of California, ducted in order to elucidate the systematics of this family. Our results do not recover the tra- UNITED STATES ditional Tergipedidae as monophyletic, since it belongs to a larger clade that includes the Received: July 7, 2016 families Eubranchidae, Fionidae and Calmidae.
    [Show full text]
  • Possible Anti-Predation Properties of the Egg Masses of the Marine Gastropods Dialula Sandiegensis, Doris Montereyensis and Haminoea Virescens (Mollusca, Gastropoda)
    Possible anti-predation properties of the egg masses of the marine gastropods Dialula sandiegensis, Doris montereyensis and Haminoea virescens (Mollusca, Gastropoda) E. Sally Chang1,2 Friday Harbor Laboratories Marine Invertebrate Zoology Summer Term 2014 1Friday Harbor Laboratories, University of Washington, Friday Harbor, WA 98250 2University of Kansas, Department of Ecology and Evolutionary Biology, Lawrence, KS 66044 Contact information: E. Sally Chang Dept. of Ecology and Evolutionary Biology University of Kansas 1200 Sunnyside Avenue Lawrence, KS 66044 [email protected] Keywords: gastropods, nudibranchs, Cephalaspidea, predation, toxins, feedimg, crustaceans Chang 1 Abstract Many marine mollucs deposit their eggs on the substrate encapsulated in distinctive masses, thereby leaving the egg case and embryos vulnerable to possible predators and pathogens. Although it is apparent that many marine gastropods possess chemical anti-predation mechanisms as an adult, it is not known from many species whether or not these compounds are widespread in the egg masses. This study aims to expand our knowledge of egg mass predation examining the feeding behavior of three species of crab when offered egg mass material from three gastropods local to the San Juan Islands. The study includes the dorid nudibranchs Diaulula sandiegensis and Doris montereyensis and the cephalospidean Haminoea virescens. The results illustrate a clear rejection of the egg masses by all three of the crab species tested, suggesting anti- predation mechanisms in the egg masses for all three species of gastropod. Introduction Eggs that are laid and then left by the parents are vulnerable to a variety of environmental stressors, both biotic and abiotic. A common, possibly protective strategy among marine invertebrates is to lay encapsulated aggregations of embryos in jelly masses (Pechenik 1978), where embryos live for all or part of their development.
    [Show full text]
  • Nudibranchia: Flabellinidae) from the Red and Arabian Seas
    Ruthenica, 2020, vol. 30, No. 4: 183-194. © Ruthenica, 2020 Published online October 1, 2020. http: ruthenica.net Molecular data and updated morphological description of Flabellina rubrolineata (Nudibranchia: Flabellinidae) from the Red and Arabian seas Irina A. EKIMOVA1,5, Tatiana I. ANTOKHINA2, Dimitry M. SCHEPETOV1,3,4 1Lomonosov Moscow State University, Leninskie Gory 1-12, 119234 Moscow, RUSSIA; 2A.N. Severtsov Institute of Ecology and Evolution, Leninskiy prosp. 33, 119071 Moscow, RUSSIA; 3N.K. Koltzov Institute of Developmental Biology RAS, Vavilov str. 26, 119334 Moscow, RUSSIA; 4Moscow Power Engineering Institute (MPEI, National Research University), 111250 Krasnokazarmennaya 14, Moscow, RUSSIA. 5Corresponding author; E-mail: [email protected] ABSTRACT. Flabellina rubrolineata was believed to have a wide distribution range, being reported from the Mediterranean Sea (non-native), the Red Sea, the Indian Ocean and adjacent seas, and the Indo-West Pacific and from Australia to Hawaii. In the present paper, we provide a redescription of Flabellina rubrolineata, based on specimens collected near the type locality of this species in the Red Sea. The morphology of this species was studied using anatomical dissections and scanning electron microscopy. To place this species in the phylogenetic framework and test the identity of other specimens of F. rubrolineata from the Indo-West Pacific we sequenced COI, H3, 16S and 28S gene fragments and obtained phylogenetic trees based on Bayesian and Maximum likelihood inferences. Our morphological and molecular results show a clear separation of F. rubrolineata from the Red Sea from its relatives in the Indo-West Pacific. We suggest that F. rubrolineata is restricted to only the Red Sea, the Arabian Sea and the Mediterranean Sea and to West Indian Ocean, while specimens from other regions belong to a complex of pseudocryptic species.
    [Show full text]
  • 09-A Report(0050)-컬러
    Anim. Syst. Evol. Divers. Vol. 30, No. 2: 124-131, April 2014 http://dx.doi.org/10.5635/ASED.2014.30.2.124 Short communication A Report on Five New Records of Nudibranch Molluscs from Korea Daewui Jung1,†, Jongrak Lee2, Chang-Bae Kim1,* 1Department of Life Science, Sangmyung University, Seoul 110-743, Korea 2Marine Biodiversity Research Institute, INTHESEA KOREA Inc., Jeju 697-110, Korea ABSTRACT The Korean nudibranch faunal study has been conducted since 2011 and five species including Dermatobran- chus otome Baba, 1992, Mexichromis festiva (Angas, 1864), Noumea nivalis Baba, 1937, Hoplodoris armata (Baba, 1993), and Okenia hiroi (Baba, 1938) were newly reported with re-descriptions and figures. Also, Noumea purpurea Baba, 1949 was re-described with illustrations because previous records for this species were given without a description. Two congeneric species in the genus Noumea could be distinguished by ground color, dorsal markings, color of the mantle edge and gills, and mantle and dorsal marking. In addition, mitochondrial cytochrome c oxidase subunit I (COI) sequences of five species were provided for further molecular identification study. Consequently, a total of 43 species have been reported for the Korean nudi- branch fauna. Keywords: Nudibranchia, taxonomy, Dermatobranchus otome, Mexichromis festiva, Noumea nivalis, Noumea purpurea, Hoplodoris armata, Okenia hiroi, Korea INTRODUCTION They were preserved in 10% neutral buffered formalin or 97 % ethanol. A stereoscopic microscope (Olympus SZ-61 with Species in the order Nudibranchia are characterized by a lack FuzhouTucsen TCA-3; Olympus, Tokyo, Japan) was used of shell in adult stage, highly diverse body form and various to examine the specimens.
    [Show full text]
  • Phyllodesmium Tuberculatum Tritonia Sp. 3 Doto Sp. H Facelina Sp. A
    Austraeolis stearnsi Hermosita hakunamatata Learchis poica Phidiana militaris Protaeolidiella juliae Moridilla brockii Noumeaella sp. 4 Cerberilla bernadettae Cerberilla sp. A Noumeaella sp. B Facelina sp. A Tritonia nilsodhneri Tritoniella belli Flabellina babai Notaeolidia depressa Tethys fimbria Armina californica Tritonia sp. F Tritonia antarctica Tritonia pickensi Leminda millecra Marianina rosea Scyllaea pelagica Pteraeolidia ianthina Limenandra sp. B 1 1 Limenandra fusiformis Limenandra sp. C 0.99 Limenandra sp. A Baeolidia nodosa 1 Spurilla sargassicola 0.82 Spurilla neapolitana 0.75 Spurilla sp. A Spurilla braziliana 1 Protaeolidiella atra Caloria indica 1 Aeolidia sp. B 0.92 Aeolidia sp. A Aeolidia papillosa 1 Glaucus atlanticus Glaucus marginatus 1 Tritonia diomedea Tritonia festiva 0.99 Hancockia californica 1 Hancockia uncinata Hancockia cf. uncinata 0.99 Spurilla creutzbergi 1 Berghia verrucicornis 0.98 Berghia coerulescens 0.91 Aeolidiella stephanieae 1 Berghia rissodominguezi 0.9 Berghia columbina Berghia sp. A 0.99 Aeolidiella sanguinea Aeolidiella alderi 0.99 Phidiana hiltoni Phidiana lynceus Armina lovenii 0.98 Armina sp. 3 Armina sp. 9 Dermatobranchus semistriatus Dermatobranchus sp. A 1 Armina semperi 0.89 Armina sp. 0.98 Dermatobranchus sp. 12 1 Dermatobranchus sp. 7 0.86 Dermatobranchus sp. 17 Dermatobranchus pustulosus 0.72 Dermatobranchus sp. 16 Dermatobranchus sp. 21 0.97 Dirona albolineata Charcotia granulosa 0.95 Baeolidia moebii 0.85 Aeolidiopsis ransoni 0.75 Baeolidia sp. A 1 Berghia salaamica 0.98 0.51 Berghia cf. salaamica 0.97 Baeolidia sp. B 0.94 Baeolidia japonica Baeolidia sp. C 0.95 Noumeaella sp. 3 Noumeaella rehderi 0.91 Cerberilla sp. B 0.57 Cerberilla sp.
    [Show full text]
  • NEWSNEWS Vol.4Vol.4 No.04: 3123 January 2002 1 4
    4.05 February 2002 Dr.Dr. KikutaroKikutaro BabaBaba MemorialMemorial IssueIssue 19052001 NEWS NEWS nudibranch nudibranch Domo Arigato gozaimas (Thank you) visit www.diveoz.com.au nudibranch NEWSNEWS Vol.4Vol.4 No.04: 3123 January 2002 1 4 1. Protaeolidella japonicus Baba, 1949 Photo W. Rudman 2, 3. Babakina festiva (Roller 1972) described as 1 Babaina. Photos by Miller and A. Ono 4. Hypselodoris babai Gosliner & Behrens 2000 Photo R. Bolland. 5. Favorinus japonicus Baba, 1949 Photo W. Rudman 6. Falbellina babai Schmekel, 1973 Photo Franco de Lorenzo 7. Phyllodesium iriomotense Baba, 1991 Photo W. Rudman 8. Cyerce kikutarobabai Hamatani 1976 - Photo M. Miller 9. Eubranchus inabai Baba, 1964 Photo W. Rudman 10. Dendrodoris elongata Baba, 1936 Photo W. Rudman 2 11. Phyllidia babai Brunckhorst 1993 Photo Brunckhorst 5 3 nudibranch NEWS Vol.4 No.04: 32 January 2002 6 9 7 10 11 8 nudibranch NEWS Vol.4 No.04: 33 January 2002 The Writings of Dr Kikutaro Baba Abe, T.; Baba, K. 1952. Notes on the opisthobranch fauna of Toyama bay, western coast of middle Japan. Collecting & Breeding 14(9):260-266. [In Japanese, N] Baba, K. 1930. Studies on Japanese nudibranchs (1). Polyceridae. Venus 2(1):4-9. [In Japanese].[N] Baba, K. 1930a. Studies on Japanese nudibranchs (2). A. Polyceridae. B. Okadaia, n.g. (preliminary report). Venus 2(2):43-50, pl. 2. [In Japanese].[N] Baba, K. 1930b. Studies on Japanese nudibranchs (3). A. Phyllidiidae. B. Aeolididae. Venus 2(3):117-125, pl. 4.[N] Baba, K. 1931. A noteworthy gill-less holohepatic nudibranch Okadaia elegans Baba, with reference to its internal anatomy.
    [Show full text]
  • Nudibranch Range Shifts Associated with the 2014 Warm Anomaly in the Northeast Pacific
    Bulletin of the Southern California Academy of Sciences Volume 115 | Issue 1 Article 2 4-26-2016 Nudibranch Range Shifts associated with the 2014 Warm Anomaly in the Northeast Pacific Jeffrey HR Goddard University of California, Santa Barbara, [email protected] Nancy Treneman University of Oregon William E. Pence Douglas E. Mason California High School Phillip M. Dobry See next page for additional authors Follow this and additional works at: https://scholar.oxy.edu/scas Part of the Marine Biology Commons, Population Biology Commons, and the Zoology Commons Recommended Citation Goddard, Jeffrey HR; Treneman, Nancy; Pence, William E.; Mason, Douglas E.; Dobry, Phillip M.; Green, Brenna; and Hoover, Craig (2016) "Nudibranch Range Shifts associated with the 2014 Warm Anomaly in the Northeast Pacific," Bulletin of the Southern California Academy of Sciences: Vol. 115: Iss. 1. Available at: https://scholar.oxy.edu/scas/vol115/iss1/2 This Article is brought to you for free and open access by OxyScholar. It has been accepted for inclusion in Bulletin of the Southern California Academy of Sciences by an authorized editor of OxyScholar. For more information, please contact [email protected]. Nudibranch Range Shifts associated with the 2014 Warm Anomaly in the Northeast Pacific Cover Page Footnote We thank Will and Ziggy Goddard for their expert assistance in the field, Jackie Sones and Eric Sanford of the Bodega Marine Laboratory for sharing their observations and knowledge of the intertidal fauna of Bodega Head and Sonoma County, and David Anderson of the National Park Service and Richard Emlet of the University of Oregon for sharing their respective observations of Okenia rosacea in northern California and southern Oregon.
    [Show full text]
  • Phidiana Lynceus Berghia Coerulescens Doto Koenneckeri
    Cuthona abronia Cuthona divae Austraeolis stearnsi Flabellina exoptata Flabellina fusca Calma glaucoides Hermosita hakunamatata Learchis poica Anteaeolidiella oliviae Aeolidiopsis ransoni Phidiana militaris Baeolidia moebii Facelina annulicornis Protaeolidiella juliae Moridilla brockii Noumeaella isa Cerberilla sp. 3 Cerberilla bernadettae Aeolidia sp. A Aeolidia sp. B Baeolidia sp. A Baeolidia sp. B Cerberilla sp. A Cerberilla sp. B Cerberilla sp. C Facelina sp. C Noumeaella sp. A Noumeaella sp. B Facelina sp. A Marionia blainvillea Aeolidia papillosa Hermissenda crassicornis Flabellina babai Dirona albolineata Doto sp. 15 Marionia sp. 10 Marionia sp. 5 Tritonia sp. 4 Lomanotus sp. E Piseinotecus sp. Dendronotus regius Favorinus elenalexiarum Janolus mirabilis Marionia levis Phyllodesmium horridum Tritonia pickensi Babakina indopacifica Marionia sp. B Godiva banyulensis Caloria elegans Favorinus brachialis Flabellina baetica 1 Facelinidae sp. A Godiva quadricolor 0.99 Limenandra fusiformis Limenandra sp. C 0.71 Limenandra sp. B 0.91 Limenandra sp. A Baeolidia nodosa 0.99 Crosslandia daedali Scyllaea pelagica Notobryon panamica Notobryon thompsoni 0.98 Notobryon sp. B Notobryon sp. C Notobryon sp. D Notobryon wardi 0.97 Tritonia sp. 3 Marionia arborescens 0.96 Hancockia cf. uncinata Hancockia californica 0.94 Spurilla chromosoma Pteraeolidia ianthina 0.92 Noumeaella sp. 3 Noumeaella rehderi 0.92 Nanuca sebastiani 0.97 Dondice occidentalis Dondice parguerensis 0.92 Pruvotfolia longicirrha Pruvotfolia pselliotes 0.88 Marionia sp. 14 Tritonia sp. G 0.87 Bonisa nakaza 0.87 Janolus sp. 2 0.82 Janolus sp. 1 Janolus sp. 7 Armina sp. 3 0.83 Armina neapolitana 0.58 Armina sp. 9 0.78 Dermatobranchus sp. 16 0.52 Dermatobranchus sp. 21 0.86 Dermatobranchus sp.
    [Show full text]
  • CREATURE CORREX Next Printing for Jane 03-12-2014
    HAWAII'S SEA CREATURE CORRECTIONS for 7th printing p. 34: BICOLOR GORGONIAN Acabaria Melithaea bicolor (Nutting, 1908) 2nd line from bottom: Known only from Hawaii Central and Western Pacific. Previously Acabaria bicolor. p. 37: DUSKY ANEMONE Anthopleura nigrescens: 2nd line from bottom: The species is reported only from Hawaii and India but is possibly more widespread. Indo-Pacific and Eastern Pacific. p. 56: LOBE CORAL 23 lines from bottom: Jonesius Cherusius triunguiculatus p. 62: BEWICK CORAL Leptastrea bewickensis Veron, Pichon, and Wijsman-Best, 1977 (add "t" at end of "Wijsman-Bes") p. 73: bottom paragraph: Free-living (turbellarian) flatworms remain a poorly known group with about 3,000 4,500 described species worldwide. Only 40-50-60 are documented from Hawai`i; more remain to be discovered and named. Twelve Thirteen species are illustrated here, all belonging to the order Polycladida. See http://www.hawaiisfishes.com/inverts/polyclad_flatworms/ for a more complete listing. p. 74: TRANSLUCENT WHITE PURSE SHELL FLATWORM Pericelis sp. hymanae (Poulter, 1974) Please replace entire text except for three last sentences: · These white flatworms are locally common under stones in shallow areas with moderate wave action, such as Black Point, O`ahu, or Kapalua Bay, Maui. Many have a narrow, brown, midbody stripe anteriorily. They appear to be associated with the Brown Purse Shell, Isognomon perna, (p. 186) and are named for American zoologist Libbie H. Hyman (1888-1969), a specialist in free-living flatworms and the author of a widely-used multivolume text on invertebrates. To almost 2 in. Known only from Hawai`i. Photo: Napili Bay, Maui.
    [Show full text]
  • Table of Contents
    ALL INDIA CO-ORDINATED PROJECT ON TAXONOMY OF MOLLUSCA ANNUAL REPORT (December 2016 – May 2018) GUJARAT STATE BOMBAY NATURAL HISTORY SOCIETY Dr. Deepak Apte Director Dr. Dishant Parasharya Dr. Bhavik Patel Scientist – B Scientist – B All India Coordinated Project on Taxonomy – Mollusca , Gujarat State Acknowledgements We are thankful to the Department of Forest and Environment, Government of Gujarat, Mr. G. K. Sinha, IFS HoFF and PCCF (Wildlife) for his guidance and cooperation in the work. We are thankful to then CCF Marine National Park and Sanctuary, Mr. Shyamal Tikader IFS, Mr. S. K. Mehta IFS and their team for the generous support, We take this opportunity to thank the entire team of Marine National Park and Sanctuary. We are thankful to all the colleagues of BNHS who directly or indirectly helped us in our work. We specially thank our field assistant, Rajesh Parmar who helped us in the field work. All India Coordinated Project on Taxonomy – Mollusca , Gujarat State 1. Introduction Gujarat has a long coastline of about 1650 km, which is mainly due to the presence of two gulfs viz. the Gulf of Khambhat (GoKh) and Gulf of Kachchh (GoK). The coastline has diverse habitats such as rocky, sandy, mangroves, coral reefs etc. The southern shore of the GoK in the western India, notified as Marine National Park and Sanctuary (MNP & S), harbours most of these major habitats. The reef areas of the GoK are rich in flora and fauna; Narara, Dwarka, Poshitra, Shivrajpur, Paga, Boria, Chank and Okha are some of these pristine areas of the GoK and its surrounding environs.
    [Show full text]