Biodiversity and Society Understanding Connections, Adapting to Change
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Volume 2, Chapter 10-2: Arthropods: Crustacea
Glime, J. M. 2017. Arthropods: Crustacea – Ostracoda and Amphipoda. Chapt. 10-2. In: Glime, J. M. Bryophyte Ecology. Volume 2. 10-2-1 Bryological Interaction. Ebook sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 19 July 2020 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology2/>. CHAPTER 10-2 ARTHROPODS: CRUSTACEA – OSTRACODA AND AMPHPODA TABLE OF CONTENTS CLASS OSTRACODA ..................................................................................................................................... 10-2-2 Adaptations ................................................................................................................................................ 10-2-3 Swimming to Crawling ....................................................................................................................... 10-2-3 Reproduction ....................................................................................................................................... 10-2-3 Habitats ...................................................................................................................................................... 10-2-3 Terrestrial ............................................................................................................................................ 10-2-3 Peat Bogs ............................................................................................................................................ 10-2-4 Aquatic ............................................................................................................................................... -
The Validity of Anthothoe Chilensis (Actiniaria, Sagartiidae) and Its Distribution in Southern Hemisphere
. THE VALIDITY OF ANTHOTHOE CHILENSIS (ACTINIARIA, SAGARTIIDAE) AND ITS DISTRIBUTION IN SOUTHERN HEMISPHERE Adriana C. Excoffon^ Maria Júlia C. Belém^ Maurício O. Zamponi^'^ Erika Schlenz^ ABSTRACT Anthothoe chilemis (Lesson, 1830) is redescribed based on specimens collected from the intertidal of Rio de Janeiro (Brazil) and Mar dei Plata (Argentina). The geographic distribution is amplified to the Southwest Atlantic Ocean. The type species of the genus, A. stimpsoni (Verrill, 1870) is considered a junior subjective synonym of A. chilensis. KEYWORDS. Sagartiidae, Anthothoe chilensis, redescription, distribution, synonymy. INTRODUCTION CARLGREN (1949) listed four species: Anthothoe stimpsoni (Verrill, 1870), A. austraUensis Carlgren, 1949, A. vagrans (Stuckey, 1909) and A. panamensis Carlgren, 1949, in the genus Anthothoe Carlgren, 1938. A. panamensis should be considered as "species inquirenda", since CARLGREN (1951: 433) identified doubtfuUy two specimens from the Gulf of California as "A. panamensis (Verrill) " CARLGREN (1950a, 1959) ixdinsíexveá Actinothoe albocincta Hutton, 1878 and Actinothoe chilensis Lesson, 1830, respectively, to the genus Anthothoe. The genus is considered as endemic to the Southern Hemisphere. 1 Laboratório de Biologia de Cnidarios. Departamento de Ciências Marinas. Faculdad de Ciências Exactas y Naturales. UNMP. Funes 3250. 7600. Mar dei Plata. Argentina. 2. Universidade Federal do Rio de Janeiro. Caixa Postal 24.030; CEP 20522-970, Rio de Janeiro, RJ, Brasil. (CNPq researcher). 3. CONICET researcher. 4. Departamento de Zoologia. Instituto de Biociências, Universidade de São Paulo, Caixa Postal 1 1 .294; CEP 05422-970, São Paulo, SP, Brasil. Iheringia, Sér. Zool., Porto Alegre, (82): 107-1 18,1 1 abr. 1997 108 EXCOFFQN; BELÉM; ZAMPONI & SCHLENZ This paper deals with the redescription ofA. -
Crustacea, Ostracoda), from Christmas Island (Indian Ocean) with Some Considerations on the Morphological Evolution of Ancient Asexuals
Belg. J. Zool., 141 (2) : 55-74 July 2011 Description of a new genus and two new species of Darwinulidae (Crustacea, Ostracoda), from Christmas Island (Indian Ocean) with some considerations on the morphological evolution of ancient asexuals Giampaolo Rossetti1*, Ricardo L. Pinto 2 & Koen Martens 3 1 University of Panna, Department of Enviromnental Sciences, Viale G.P. Usberti 33 A, 1-43100 Panna, Italy 2 University of Brasilia, Institute of Geosciences, Laboratory of Micropaleontology, ICC, Campus Universitário Darcy Ribeiro Asa Norte, 70910-900 Brasilia, DF, Brazil 3 Royal Belgian Institute of Natural Sciences, Freshwater Biology, Vautierstraat 29, B-1000 Brussels, Belgium, and University of Ghent, Department of Biology, K.L. Ledeganckstraat 35, B-9000 Gent, Belgimn * Conesponding author: Giampaolo Rossetti. Mail: giampaolo.rosscttin unipr.it ABSTRACT. Darwinulidae is believed to be one of the few metazoan taxa in which fully asexual reproduction might have persisted for millions of years. Although rare males in a single darwinulid species have recently been found, they may be non-functional atavisms. The representatives of this family are characterized by a slow evolutionary rate, resulting in a conservative morphology in the different lineages over long time frames and across wide geographic ranges. Differences between species and genera, although often based on small details of valve morphology and chaetotaxy, are nevertheless well-recognizable. Five recent genera ( Darwinula, Alicenula, Vestcdemilct, Penthesilemila and Microdarwimda) and about 35 living species, including also those left in open nomenclature, are included in this family. Previous phylogenetic analyses using both morphological characters and molecular data confirmed that the five genera are good phyletic units. -
Ostracoda, Crustacea) in Turkey
LIMNOFISH-Journal of Limnology and Freshwater Fisheries Research 5(1): 47-59 (2019) Fossil and Recent Distribution and Ecology of Ancient Asexual Ostracod Darwinula stevensoni (Ostracoda, Crustacea) in Turkey Mehmet YAVUZATMACA * , Okan KÜLKÖYLÜOĞLU Department of Biology, Faculty of Arts and Science, Bolu Abant İzzet Baysal University, Turkey ABSTRACT ARTICLE INFO In order to determine distribution, habitat and ecological preferences of RESEARCH ARTICLE Darwinula stevensoni, data gathered from 102 samples collected in Turkey between 2000 and 2017 was evaluated. A total of 1786 individuals of D. Received : 28.08.2018 stevensoni were reported from eight different aquatic habitats in 14 provinces in Revised : 21.10.2018 six of seven geographical regions of Turkey. Although there are plenty of samples Accepted : 30.10.2018 from Central Anatolia Region, recent form of the species was not encountered. Unlike recent, fossil forms of species were encountered in all geographic regions Published : 25.04.2019 except Southeastern Anatolia. The oldest fossil record in Turkey was reported from the Miocene period (ca 23 mya). Species occurred in all climatic seasons in DOI:10.17216/LimnoFish.455722 Turkey. D. stevensoni showed high optimum and tolerance levels to different ecological variables. Results showed a positive and negative significant * CORRESPONDING AUTHOR correlations of the species with pH (P<0.05) and elevation (P<0.01), respectively. [email protected] It seems that the ecological preferences of the species are much wider than Phone : +90 537 769 46 28 previously known. Our results suggest that if D. stevensoni is used to estimate past and present environmental conditions, attention and care should be paid on its ecology and distribution. -
On Two New Species of Darwinula BRADY & ROBERTSON, 1885
BULLETIN DE L'INSTITUT ROYAL DES SCIENCES NATURELLES DE BELGIQUE, BIOLOGIE, 67: 57-66, 1997 '' BULLETIN VAN HET KONrNKLIJK BELGISCH INSTITUUT VOOR NATUURWETENSCHAPPEN, BIOLOGIE, 67: 57-66, 1997 On two new species of Darwinula BRADY & ROBERTSON, 1885 (Crustacea, Ostracoda) from South African dolomitic springs by Koen MARTENS & Giampaolo ROSSETTI Abstract 1968 (represented by only one extant spec1es, M. zimmeri) and the nominate genus Danvinula BRADY Two new Recent darwinulid ostrac ds (Darwinu/a molopoensis & ROB ERTSON, 1885. SOHN (1987) reported 23 living spec. nov. and D. inversa spec. nov.) are described from dolomitic species and 2 subspecies for Darwinula (D. dicastrii springs in the former North West Province (the former Transvaal), LOFFLER was missing from this list); amon·g these RSA. The two new taxa can be distinguished by both soft part species, only D. stevensoni can be considered truly and valve morphology. Darwinula molopoensis spec. nov. belongs ubiquitous. to the D. africana lineage (with D. incon5picua KuE as its Except for a few papers on D. stevensoni (McGREGOR & closest relative), D. inversa spec. nov. belongs into the D. serricaudata group. The synonymy of D. serricaudata espinosa WETZEL 1968, MCGREGOR 1969; RANTA, 1979), little is PINTO & KOTZIAN, 1961 with D. serricaudata KLIE, 1935 is known on the biology and ecology of the Darwinuloidea. discussed. Also taxonomic relationships within this group remain Key words: Ostracods, Darwinu/a mo/opoensis spec. nov., " "unclear, in s'pite of valuable contributions by DAN IELOPOL Darwinula inversa spec. nov., morphology, taxonomy, ancient (1968, 1970, 1980). Indeed, the morphological uniformity asexuals, parthenogenesis, biodiversity. of the Darwinuloidea makes it difficult to single out unequivocal characters suitable for discriminating species and genera. -
Estudio De Las Toxinas De La Anémona De Mar Anthothoe Chilensis (Lesson
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is padres Juan y Yojana, que son mis mejores guías Mis hermanos Sara, Juan y Yanet amigos incondicionales Mis abuelitas Mercedes Rosas por todo su cariño y consejos, y Luz Garcés A la memoria de mis abuelitos Melecio Quiroz y Jorge Garrido Por su ejemplo de perseverancia y optimismo… -'% (. */ 0 $1 ! " - 2 ! !" ## $# %& '()* % $"+ ,"* 3 -'% (. */ 0 $1 ! " - 0 5 0 5 Agradezco a Dios por la oportunidad de haber realizado y terminado satisfactoriamente este proyecto y por haber puesto en mi camino muchas personas extraordinarias que me han apoyado desinteresadamente. A mis padres Juan y Yojana, a mis hermanos Sara, Juan y Yanet, por su paciencia y comprensión en la espera de la culminación de este trabajo. -
Index Seminum 2018-2019
UNIVERSITÀ DEGLI STUDI DI NAPOLI FEDERICO II ORTO BOTANICO INDEX SEMINUM 2018-2019 In copertina / Cover “La Terrazza Carolina del Real Orto Botanico” Dedicata alla Regina Maria Carolina Bonaparte da Gioacchino Murat, Re di Napoli dal 1808 al 1815 (Photo S. Gaudino, 2018) 2 UNIVERSITÀ DEGLI STUDI DI NAPOLI FEDERICO II ORTO BOTANICO INDEX SEMINUM 2018 - 2019 SPORAE ET SEMINA QUAE HORTUS BOTANICUS NEAPOLITANUS PRO MUTUA COMMUTATIONE OFFERT 3 UNIVERSITÀ DEGLI STUDI DI NAPOLI FEDERICO II ORTO BOTANICO ebgconsortiumindexseminum2018-2019 IPEN member ➢ CarpoSpermaTeca / Index-Seminum E- mail: [email protected] - Tel. +39/81/2533922 Via Foria, 223 - 80139 NAPOLI - ITALY http://www.ortobotanico.unina.it/OBN4/6_index/index.htm 4 Sommario / Contents Prefazione / Foreword 7 Dati geografici e climatici / Geographical and climatic data 9 Note / Notices 11 Mappa dell’Orto Botanico di Napoli / Botanical Garden map 13 Legenda dei codici e delle abbreviazioni / Key to signs and abbreviations 14 Index Seminum / Seed list: Felci / Ferns 15 Gimnosperme / Gymnosperms 18 Angiosperme / Angiosperms 21 Desiderata e condizioni di spedizione / Agreement and desiderata 55 Bibliografia e Ringraziamenti / Bibliography and Acknowledgements 57 5 INDEX SEMINUM UNIVERSITÀ DEGLI STUDI DI NAPOLI FEDERICO II ORTO BOTANICO Prof. PAOLO CAPUTO Horti Praefectus Dr. MANUELA DE MATTEIS TORTORA Seminum curator STEFANO GAUDINO Seminum collector 6 Prefazione / Foreword L'ORTO BOTANICO dell'Università ha lo scopo di introdurre, curare e conservare specie vegetali da diffondere e proteggere, -
Biodiversity of Chilean Sea Anemones (Cnidaria: Anthozoa): Distribution Patterns and Zoogeographic Implications, Including New Records for the Fjord Region*
Invest. Mar., Valparaíso, 34(2): 23-35, 2006 Biogeography of Chilean sea anemones 23 Biodiversity of Chilean sea anemones (Cnidaria: Anthozoa): distribution patterns and zoogeographic implications, including new records for the fjord region* Verena Häussermann Fundación Huinay, Departamento de Biología Marina, Universidad Austral de Chile Casilla 567, Valdivia, Chile ABSTRACT. The present paper provides a complete zoogeographical analysis of the sea anemones (Actiniaria and Corallimorpharia) of continental Chile. The species described in the primary literature are listed, including depth and distribution records. Records and the taxonomic status of many eastern South Pacific species are doubtful and need revision and confirmation. Since 1994, we have collected more than 1200 specimens belonging to at least 41 species of Actiniaria and Corallimorpharia. We sampled more than 170 sites along the Chilean coast between Arica (18°30’S, 70°19’W) and the Straits of Magellan (53°36’S, 70°56’W) from the intertidal to 40 m depth. The results of three recent expeditions to the Guaitecas Islands (44°S) and the Central Patagonian Zone (48°-52°S) are included in this study. In the fjord Comau, an ROV was used to detect the bathymetrical distribution of sea anemones down to 255 m. A distribution map of the studied shallow water sea anemones is given. The northern part of the fjord region is inhabited by the most species (27). The results show the continuation of species characteristic for the exposed coast south of 42°S and the joining of typical fjord species at this latitude. This differs from the classical concept of an abrupt change in the faunal composition south of 42°S. -
Effect of Temperature on Seed Germination of Bombax Costatum Pellegr
Brazilian Journal of Biological Sciences, 2019, Vol. 6, No. 13, p. 439-443. ISSN 2358-2731 https://doi.org/10.21472/bjbs.061311 Effect of temperature on seed germination of Bombax costatum Pellegr. & Vuill. (Malvales: Malvaceae) from Ondo and Oyo States, Nigeria M. O. Ojo Forestry Research Institute of Nigeria. P.M.B. 5054 Ibaban. Oyo State. Nigeria. Email: [email protected]. Abstract. Effect of temperature on seed germination of Bombax costatum Pellegr & Vuill. (Malvales: Malvaceae), from four Received provenances in South Western Nigeria was investigated. A set of May 29, 2019 three replicates of 25 seeds per provenance were used for the experiment which was laid in a completely randomized block Accepted August 26, 2019 design. The seeds were exposed to fire temperature regimes for germination tests: 28 °C, 20 °C, 5 °C, 35 °C and 20 °C. Seed Released germination was recorded for 4 weeks. Data obtained were August 31, 2019 subjected to analysis of variance. Result showed that significant differences in seed germination under varying temperature Full Text Article regimes (P < 0.05). Interaction effect between temperature and provenances was not significant (P < 0.05). seeds placed in ambient temperature had the highest mean number of germination (20.75) while the least mean value (0.17) was observed for cold room (-20 °C). B. costatum seeds should be exposed to ambient temperature so as to promote seed germination. Keywords: Red-flowered silk cotton tree; Seed germination provenances; Temperature. 0000-0003-0750-4431 M. O. Ojo Introduction the largest traditional forest product imported into Nigeria. In Nigeria, a high proportion of Osadare (1995) and National forests have changed an extent reduced Agricultural Research Project (NARP, by man’s activities such as farming, 1995), investigated the suitability of overgrazing, use of fire for forest clearing some deciduous tree species as as well as over exploitation without substitute sources of raw materials and replacement. -
Appendix 1 Vernacular Names
Appendix 1 Vernacular Names The vernacular names listed below have been collected from the literature. Few have phonetic spellings. Spelling is not helped by the difficulties of transcribing unwritten languages into European syllables and Roman script. Some languages have several names for the same species. Further complications arise from the various dialects and corruptions within a language, and use of names borrowed from other languages. Where the people are bilingual the person recording the name may fail to check which language it comes from. For example, in northern Sahel where Arabic is the lingua franca, the recorded names, supposedly Arabic, include a number from local languages. Sometimes the same name may be used for several species. For example, kiri is the Susu name for both Adansonia digitata and Drypetes afzelii. There is nothing unusual about such complications. For example, Grigson (1955) cites 52 English synonyms for the common dandelion (Taraxacum officinale) in the British Isles, and also mentions several examples of the same vernacular name applying to different species. Even Theophrastus in c. 300 BC complained that there were three plants called strykhnos, which were edible, soporific or hallucinogenic (Hort 1916). Languages and history are linked and it is hoped that understanding how lan- guages spread will lead to the discovery of the historical origins of some of the vernacular names for the baobab. The classification followed here is that of Gordon (2005) updated and edited by Blench (2005, personal communication). Alternative family names are shown in square brackets, dialects in parenthesis. Superscript Arabic numbers refer to references to the vernacular names; Roman numbers refer to further information in Section 4. -
Crustacea: Ostracoda) De Pozas Temporales
Heterocypris bosniaca (Petkowski et al., 2000): Ecología y ontogenia de un ostrácodo (Crustacea: Ostracoda) de pozas temporales. ESIS OCTORAL T D Josep Antoni Aguilar Alberola Departament de Microbiologia i Ecologia Universitat de València Programa de doctorat en Biodiversitat i Biologia Evolutiva Heterocypris bosniaca (Petkowski et al., 2000): Ecología y ontogenia de un ostrácodo (Crustacea: Ostracoda) de pozas temporales. Tesis doctoral presentada por Josep Antoni Aguilar Alberola 2013 Dirigida por Francesc Mesquita Joanes Imagen de cubierta: Vista lateral de la fase eclosionadora de Heterocypris bosniaca. Más detalles en el capítulo V. Tesis titulada "Heterocypris bosniaca (Petkowski et al., 2000): Ecología y ontogenia de un ostrácodo (Crustacea: Ostracoda) de pozas temporales" presentada por JOSEP ANTONI AGUILAR ALBEROLA para optar al grado de Doctor en Ciencias Biológicas por la Universitat de València. Firmado: Josep Antoni Aguilar Alberola Tesis dirigida por el Doctor en Ciencias Biológicas por la Universitat de València, FRANCESC MESQUITA JOANES. Firmado: F. Mesquita i Joanes Profesor Titular de Ecología Universitat de València A Laura, Paco, i la meua família Resumen Los ostrácodos son un grupo de pequeños crustáceos con amplia distribución mundial, cuyo cuerpo está protegido por dos valvas laterales que suelen preservarse con facilidad en el sedimento. En el presente trabajo se muestra la primera cita del ostrácodo Heterocypris bosniaca Petkowski, Scharf y Keyser, 2000 para la Península Ibérica. Se trata de una especie de cipridoideo muy poco conocida que habita pozas de aguas temporales. Se descubrió el año 2000 en Bosnia y desde entonces solo se ha reportado su presencia en Israel (2004) y en Valencia (presente trabajo). -
Mikro-Originale Sammlung BGR/LBEG Hannover
Mikro-Originale Sammlung BGR/LBEG Hannover Al-Abawi, T. (1973) Miozäne Foraminiferen aus dem NE-Irak. (Miocene foraminifera from the NE Iraq). N.Jb. Geol. Paläont. Abh., 144, 1: 1-23, 9 Abb.; Stuttgart. ? Dorothia sp. Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 55 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 47 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 48 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 49 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 50 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 51 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 52 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 62 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 54 Belegexemplar Ammonia acuta n. sp. Abb. 5, Fig. 42c Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 56 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 57 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 58 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 59 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 60 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 61 Belegexemplar Ammonia acuta n. sp. Abb. 6, Fig. 53 Belegexemplar Ammonia acuta n. sp. Abb. 5, Fig. 35c Belegexemplar Ammonia acuta n. sp. Abb. 5, Fig. 27a-c Holotypus Ammonia acuta n. sp. Abb. 5, Fig. 28a-c Paratypus Ammonia acuta n. sp. Abb. 5, Fig. 29a-c Paratypus Ammonia acuta n. sp. Abb. 5, Fig. 30a-c Belegexemplar Ammonia acuta n. sp. Abb. 5, Fig. 31c Belegexemplar Ammonia acuta n. sp. Abb. 5, Fig. 32c Belegexemplar Ammonia acuta n.