An Illustrated Key to the Fiddler Crabs (Crustacea, Decapoda, Ocypodidae) from the Atlantic Coast of Brazil
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On the Crabs of the Family Ocypodidae in the Collection of the Raffles Museum M. W. F. TWEEDIE
Reprint from Bulletin of the Raffles Museum, Singapore, Straits Settlements, No. IS, August 1937 On the Crabs of the family Ocypodidae in the collection of the Raffles Museum hy M. W. F. TWEEDIE M. W. F. TWEEDIE On the Crabs of the Family Ocypodidae in the Collection of the Raffles Museum By M. W. F. TwEEDiE, M.A. The material described in this paper has been collected for the most part during the last four years, mainly in mangrove swamps around Singapore Island and at a few localities on the east and west coasts of the Malay Peninsula. The greater part of the paper and most of the figures were prepared at the British Museum (Natural History) during August and September, 1936, and my grateful acknowledgments are due to the Director for permission to work there and for facilities provided, and particularly to Dr. Isabella Gordon for her unfailing help and encouragement. I wish also to express my thanks to the Directorates of the Zoological Museums at Leiden and Amsterdam for permission to examine types, and for the helpfulness and courtesy with which I was received by the members of the staffs of these museums. Finally acknowledgments are due to Prof. Dr. H. Balss, Dr. B. N. Chopra and Dr. C. J. Shen for their kindness in comparing specimens with types and authentic specimens in their respective institutions. The mode adopted for collecting the material may be of interest to collectors of Crustacea, and possibly other invertebrate groups, in the tropics. It was found that if crabs, especially Grapsidse and Ocypodidse, are put straight into alcohol, they tend to die slowly and in their struggles to shed their limbs and damage each other, so that often less than 10% of the collection survive as perfect specimens. -
A Systematic and Experimental Analysis of Their Genes, Genomes, Mrnas and Proteins; and Perspective to Next Generation Sequencing
Crustaceana 92 (10) 1169-1205 CRUSTACEAN VITELLOGENIN: A SYSTEMATIC AND EXPERIMENTAL ANALYSIS OF THEIR GENES, GENOMES, MRNAS AND PROTEINS; AND PERSPECTIVE TO NEXT GENERATION SEQUENCING BY STEPHANIE JIMENEZ-GUTIERREZ1), CRISTIAN E. CADENA-CABALLERO2), CARLOS BARRIOS-HERNANDEZ3), RAUL PEREZ-GONZALEZ1), FRANCISCO MARTINEZ-PEREZ2,3) and LAURA R. JIMENEZ-GUTIERREZ1,5) 1) Sea Science Faculty, Sinaloa Autonomous University, Mazatlan, Sinaloa, 82000, Mexico 2) Coelomate Genomic Laboratory, Microbiology and Genetics Group, Industrial University of Santander, Bucaramanga, 680007, Colombia 3) Advanced Computing and a Large Scale Group, Industrial University of Santander, Bucaramanga, 680007, Colombia 4) Catedra-CONACYT, National Council for Science and Technology, CDMX, 03940, Mexico ABSTRACT Crustacean vitellogenesis is a process that involves Vitellin, produced via endoproteolysis of its precursor, which is designated as Vitellogenin (Vtg). The Vtg gene, mRNA and protein regulation involve several environmental factors and physiological processes, including gonadal maturation and moult stages, among others. Once the Vtg gene, mRNAs and protein are obtained, it is possible to establish the relationship between the elements that participate in their regulation, which could either be species-specific, or tissue-specific. This work is a systematic analysis that compares the similarities and differences of Vtg genes, mRNA and Vtg between the crustacean species reported in databases with respect to that obtained from the transcriptome of Callinectes arcuatus, C. toxotes, Penaeus stylirostris and P. vannamei obtained with MiSeq sequencing technology from Illumina. Those analyses confirm that the Vtg obtained from selected species will serve to understand the process of vitellogenesis in crustaceans that is important for fisheries and aquaculture. RESUMEN La vitelogénesis de los crustáceos es un proceso que involucra la vitelina, producida a través de la endoproteólisis de su precursor llamado Vitelogenina (Vtg). -
Occurrence of Ocypode Cursor (Linnaeus, 1758) (Crustacea, Decapoda) in Salento (Southern Italy)
View metadata, citation and similar papers at core.ac.uk brought to you by CORE Thalassia Salentina provided by ESE - Salento University Publishing Thalassia Sal. 41 (2019), 47-52 ISSN 0563-3745, e-ISSN 1591-0725 DOI 10.1285/i15910725v41p47 http: siba-ese.unisalento.it - © 2019 Università del Salento GIORGIO MANCINELLI1,2,3*, FRANCESCO BELMONTE4, GENUARIO BELMONTE1,3 1 Department of Biological and Environmental Sciences and Technologies (DiSTeBA), University of Salento, 73100 Lecce, Italy 2 National Research Council (CNR), Institute of Biological Resources and Marine Biotechnologies (IRBIM), Lesina - (FG), Italy 3 CoNISMa, Consorzio Nazionale Interuniversitario per le Scienze del Mare, 00196 Roma, Italy 4 via G. Casciaro, 73100 Lecce, Italy * corresponding author: [email protected] OCCURRENCE OF OCYPODE CURSOR (LINNAEUS, 1758) (CRUSTACEA, DECAPODA) IN SALENTO (SOUTHERN ITALY) SUMMARY Ocypode cursor (Linnaeus, 1758) is the only Ocypode species present in the Mediterranean Sea. It is widely distributed in the southern part of the basin (mainly African coast) and only recently it has been reported also from Sicil- ian Ionian sea. The present record is the first for Italian peninsula and the northernmost record of O. cursor in the Mediterranen Sea. INTRODUCTION The tufted ghost crab Ocypode cursor (Linnaeus, 1758) is a semi-terrestrial burrowing brachyuran of nocturnal habits generally found in supratidal and intertidal sandy beaches (STRACHAN et al., 1999). The species is the only member of the family Ocypodidae occurring in the Mediterranean Sea; specifically, it is characterized by a disjoint distribu- tion, comprising the eastern Mediterranean Sea and tropical coasts of the eastern Atlantic Ocean as far south as northern Namibia, with the exclusion of the western Mediterranean. -
From Ghost and Mud Shrimp
Zootaxa 4365 (3): 251–301 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2017 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4365.3.1 http://zoobank.org/urn:lsid:zoobank.org:pub:C5AC71E8-2F60-448E-B50D-22B61AC11E6A Parasites (Isopoda: Epicaridea and Nematoda) from ghost and mud shrimp (Decapoda: Axiidea and Gebiidea) with descriptions of a new genus and a new species of bopyrid isopod and clarification of Pseudione Kossmann, 1881 CHRISTOPHER B. BOYKO1,4, JASON D. WILLIAMS2 & JEFFREY D. SHIELDS3 1Division of Invertebrate Zoology, American Museum of Natural History, Central Park West @ 79th St., New York, New York 10024, U.S.A. E-mail: [email protected] 2Department of Biology, Hofstra University, Hempstead, New York 11549, U.S.A. E-mail: [email protected] 3Department of Aquatic Health Sciences, Virginia Institute of Marine Science, College of William & Mary, P.O. Box 1346, Gloucester Point, Virginia 23062, U.S.A. E-mail: [email protected] 4Corresponding author Table of contents Abstract . 252 Introduction . 252 Methods and materials . 253 Taxonomy . 253 Isopoda Latreille, 1817 . 253 Bopyroidea Rafinesque, 1815 . 253 Ionidae H. Milne Edwards, 1840. 253 Ione Latreille, 1818 . 253 Ione cornuta Bate, 1864 . 254 Ione thompsoni Richardson, 1904. 255 Ione thoracica (Montagu, 1808) . 256 Bopyridae Rafinesque, 1815 . 260 Pseudioninae Codreanu, 1967 . 260 Acrobelione Bourdon, 1981. 260 Acrobelione halimedae n. sp. 260 Key to females of species of Acrobelione Bourdon, 1981 . 262 Gyge Cornalia & Panceri, 1861. 262 Gyge branchialis Cornalia & Panceri, 1861 . 262 Gyge ovalis (Shiino, 1939) . 264 Ionella Bonnier, 1900 . -
Crustacea: Decapoda: Ocypodidae
Zoological Studies 44(2): 242-251 (2005) Chimney Building by Male Uca formosensis Rathbun, 1921 (Crustacea: Decapoda: Ocypodidae) after Pairing: A New Hypothesis for Chimney Function Hsi-Te Shih1,2,*, Hin-Kiu Mok2, and Hsueh-Wen Chang3 1Department of Life Science, National Chung-Hsing University, Taichung, Taiwan 402, R.O.C. Tel/Fax: 886-4-22856496. E-mail: [email protected] 2Institute of Marine Biology, National Sun Yat-sen University, Kaohsiung, Taiwan 804, R.O.C. 3Department of Biological Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan 804, R.O.C. (Accepted February 8, 2005) Hsi-Te Shih, Hin-Kiu Mok, and Hsueh-Wen Chang (2005) Chimney building by male Uca formosensis Rathbun, 1921 (Crustacea: Decapoda: Ocypodidae) after pairing: a new hypothesis for chimney function. Zoological Studies 44(2): 242-251. The construction of a chimney after pairing is first described for Uca for- mosensis Rathbun, 1921, a fiddler crab endemic to Taiwan. After attracting a female into his burrow, the male builds a chimney averaging 9.2 cm high and 7.7 cm in diameter at the base within a 4- or 5-d period before the next neap tide. It is not related to sexual attraction because the chimney does not appear prior to or during courtship. To build the chimney, the male excavates the burrow which probably widens the shaft and, more importantly, deepens the burrow so that it reaches the water table, thus providing a moist chamber in which the female can incubate her eggs. The mudballs dug out from within the burrow are piled around the entrance and form the chimney, which herein is assumed to function as a way for the builder to hide from its enemies. -
Burrow Architectural Types of the Atlantic Ghost Crab, Ocypode Quadrata (Fabricius
bioRxiv preprint doi: https://doi.org/10.1101/006098; this version posted July 25, 2014. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Burrow architectural types of the Atlantic ghost crab, Ocypode quadrata (Fabricius, 2 1787) (Brachyura: Ocypodidae), in Brazil 3 4 WILLIAN T. A. F. SILVA1,2, TEREZA C. S. CALADO1 5 6 1Integrated Laboratories of Marine and Natural Sciences (LabMar), Federal University of 7 Alagoas (UFAL), Avenida Aristeu de Andrade, 452, Farol, CEP 57051-090, Maceió, 8 Alagoas, Brazil. 9 2Current affiliation: Department of Evolutionary Biology (Ecology and Genetics), 10 Evolutionary Biology Center (EBC), Uppsala University, Uppsala, Sweden. 11 Corresponding author: WTAFS, [email protected] 12 13 Running title: Shapes of ghost crab burrows 14 15 Abstract: A broad range of aspects from paleontology to physiology of the ghost crabs 16 Ocypode quadrata have been studied worldwide. These crabs have been used as ecological 17 indicators of the levels of anthropogenic impacts on sandy beaches. Our aim is to report the 18 variety of burrow architecture types constructed by ghost crabs Ocypode quadrata on 19 beaches of Maceió, Brazil. We found 20 types of burrows that differ in shape (number of 20 axes, number of openings, orientation of blind end, number of branches). The slash-shaped 21 burrows (type C) were the most frequent shape, followed by types K (spiral) and E (Y- 22 shaped). -
Description of the First Juvenile Stage of the Fiddler Crab Minuca Mordax (Smith, 1870) (Crustacea, Decapoda, Ocypodidae)
Volume 56(14):163‑169, 2016 DESCRIPTION OF THE FIRST JUVENILE STAGE OF THE FIDDLER CRAB MINUCA MORDAX (SMITH, 1870) (CRUSTACEA, DECAPODA, OCYPODIDAE) SALISE BRANDT MARTINS¹² MURILO ZANETTI MAROCHI¹³ SETUKO MASUNARI¹⁴ ABSTRACT The first stage of the fiddler crab Minuca mordax is described here. Zoea larvae obtained from four ovigerous female were reared in the laboratory until the development of the first crab stage. The development from zoea I to the first juvenile instar lasted 35 days after hatching. The first crab stage of Minuca mordax can be morphologically distinguished from those of Minuca burgersi and Leptuca cumulanta by a 2‑segmented antennule endopod (3‑segmented in M. burgersi, unsegmented in L. cumulanta), an unsegmented maxillule endopod (2‑seg‑ mented in M. burgersi and L. cumulanta), and a 4‑segmented first and second maxilliped endopod (respectively unsegmented and 5‑segmented in M. burgersi and L. cumulanta). The three species have the following characters in common: segmented peduncle of antennule 2; endopod of antennule unsegmented; presence of aesthetascs on the antennule; peduncle of an‑ tenna 3‑segmented; flagellum of antenna 6‑segmented; mandible 3‑segmented; maxilla with coxal and basal endite bilobed; first, second and third maxillae with exopod 2‑segmented and abdomen with six somites that are wider than long. Key-Words: Juvenile morphology; Development; Mangrove; Guaratuba Bay. INTRODUCTION Minuca mordax (Smith, 1870). This species is distrib- uted in the Western Atlantic Ocean, from the Gulf The former fiddler crab genus Uca Leach, 1814 of Mexico to the Rio Grande do Sul state, southern was composed of approximately 104 species, with 12 Brazil (Bezerra, 2012). -
Uca Rapax (Mudflat Fiddler Crab)
UWI The Online Guide to the Animals of Trinidad and Tobago Ecology Uca rapax (Mudflat Fiddler Crab) Order: Decapoda (Crabs, Lobsters and Shrimps) Class: Malacostraca (Crustaceans: Crabs, Sand-hoppers and Woodlice) Phylum: Arthropoda (Arthropods) Fig. 1. Mudflat fiddler crab, Uca rapax. [http://ocean.si.edu/mangroves, downloaded 10 March 2016] TRAITS. The mudflat fiddler crab Uca rapax is considered dimorphic since the males have a large claw on one side of the body (Fig. 1) and the females have two small claws. Males are also larger in body size: in Brazil, the carapace width at maturity was 13-15mm in males and 11- 12mm in females (Castiglioni and Negreiros-Fransozo, 2004). Both females and males are generally greyish-white in colour, but green to blue can be seen in the large claw and the eyestalks. Colour is dependent upon environmental factors, and hints of orange and yellow are also found in the claws. Fiddler crabs are darker during the day time and light during the night (Tpwd.Texas.Gov., 2016). DISTRIBUTION. Uca rapax is found along tropical coasts of the USA (southern Florida, Texas), West Indies and the Caribbean, and Brazil (Fig. 2). HABITAT AND ACTIVITY. As the name suggests (mud fiddler crab), they reside in intertidal zones of muddy areas of the salt marsh and mangroves (Figueiredo et al., 2008) (Fig. 3). The soft mud is not only home to these creatures but also their feeding ground and protection. Uca rapax are diurnal, skilled at burrowing into the mud, creating holes that provide a nest for their young, privacy for mating, for sleeping and in the colder regions “hibernation” during the winter UWI The Online Guide to the Animals of Trinidad and Tobago Ecology (Gcrl.Usm.Edu., 2016). -
Bioecology of the Ghost Crab Ocypode Quadrata (Fabricius, 1787) (Crustacea: Brachyura) Compared with Other Intertidal Crabs in the Southwestern Atlantic
Journal of Shellfish Research, Vol. 29, No. 2, 503–512, 2010. BIOECOLOGY OF THE GHOST CRAB OCYPODE QUADRATA (FABRICIUS, 1787) (CRUSTACEA: BRACHYURA) COMPARED WITH OTHER INTERTIDAL CRABS IN THE SOUTHWESTERN ATLANTIC JOAQUIM O. BRANCO,1 JULIANO C. HILLESHEIM,1 HE´LIO A. A. FRACASSO,2 MARTIN L. CHRISTOFFERSEN3* AND CRISTIANO L. EVANGELISTA1 1Centro de Cieˆncias Tecnolo´gicas da Terra e do Mar (CTTMar), Universidade Vale do Itajaı´ (UNIVALI), CP 360, 88302-202 Itajaı´, SC, Brazil; 2Departamento de Hidrobiologia, Universidade Federal de Sa˜o Carlos (UFSCar), 13565-905, Sa˜o Carlos, SP, Brazil; 3Departamento de Sistema´tica e Ecologia, Universidade Federal da Paraı´ba, 58059-900, Joa˜o Pessoa, PB, Brazil ABSTRACT Data sets on the natural dynamics of beach ecosystems are scarce and fragmentary. Such data are necessary for implementing more efficient monitoring programs that quantify the dynamics of key ecological attributes on sandy beaches. This article contributes to the bioecology of ghost crabs from subtropical Praia Brava, Itajaı´, Santa Catarina. Ocypode quadrata occurs in sandy beaches along the tropical–temperate western Atlantic, from Rhode Island (US) to Rio Grande do Sul (Brazil). During 14 consecutive months, a total of 649 specimens were captured: 255 females (39%), 241 males (37%), and 153 juveniles of undetermined sex (24%). Highest densities were recorded in June and November, with a total of 1,900 burrows distributed along the beach (56.95%) and dunes (43.05%). Sixteen natural diet items were identified for this crab, with a larger participation of Apis spp. (38.97% of relative volume). In the local food web, the ground-burrowing owl Speotyto cunicularia was the main crab predator. -
Species Diversity of Fiddler Crabs, Genus Uca Leach, 1814 (Crustacea: Ocypodidae), from Taiwan and Adjacent Islands, with Notes on the Japanese Species
Zootaxa 4083 (1): 057–082 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4083.1.3 http://zoobank.org/urn:lsid:zoobank.org:pub:FC132216-6CFB-4E3F-B166-6F9BE3C50588 Species diversity of fiddler crabs, genus Uca Leach, 1814 (Crustacea: Ocypodidae), from Taiwan and adjacent islands, with notes on the Japanese species HSI-TE SHIH1, JUNG-HSIANG LEE2, PING-HO HO3,8, HUNG-CHANG LIU4, CHIA-HSIANG WANG5,6, HIROSHI SUZUKI7 & SHAO-JYUN TENG1 1Department of Life Science, National Chung Hsing University, 250, Kuo Kuang Road, Taichung 402, Taiwan. E-mail: [email protected] 2Center for General Education, National University of Tainan, 33, Sec. 2, Shulin Street, Tainan City 700, Taiwan. 3Department of Environment Biology and Fishery Science, National Taiwan Ocean University, 2 Pei-Ning Road, Keelung 202, Taiwan. 453, Chenggong 11th St., Zhubei City, Hsinchu County 302, Taiwan 5National Taiwan Museum, 6F, 71 Guanqian Road, Taipei 10047, Taiwan. 61-1 Alley 24, Lane 417 Tzechiang Road, New Taipei City 25162, Taiwan 7Faculty of Fisheries, Kagoshima University, Shimoarata 4-50-20, Kagoshima City, 890-0056, Japan 8Corresponding author. E-mail: [email protected] Abstract The fiddler crabs, genus Uca Leach, 1814 (Decapoda, Ocypodidae) of Taiwan, including the offshore islands of Penghu (Pescadores), Kinmen (Quemoy), Matsu (Matzu), and Dongsha (Pratas), are revised, with the recognition of five subgen- era and 15 species, viz. Uca (Austruca) Bott, 1973: U. lactea (De Haan, 1835), U. perplexa (H. Milne Edwards, 1837), U. -
Human Threats to Sandy Beaches – a Meta-Analysis of Ghost Crabs
Estuarine, Coastal and Shelf Science 169 (2016) 56e73 Contents lists available at ScienceDirect Estuarine, Coastal and Shelf Science journal homepage: www.elsevier.com/locate/ecss Human threats to sandy beaches: A meta-analysis of ghost crabs illustrates global anthropogenic impacts. * Thomas A. Schlacher a, , Serena Lucrezi b, Rod M. Connolly c, Charles H. Peterson d, Ben L. Gilby a, Brooke Maslo e, Andrew D. Olds a, Simon J. Walker a, Javier X. Leon a, Chantal M. Huijbers a, Michael A. Weston f, Alexander Turra g, Glenn A. Hyndes h, Rebecca A. Holt c, David S. Schoeman a a School of Science and Engineering, The University of the Sunshine Coast, Q-4558, Maroochydore, Australia b TREESdTourism Research in Economic Environs and Society, North-West University, Potchefstroom, South Africa c Australian Rivers Institute e Coast & Estuaries, and School of Environment, Gold Coast Campus, Griffith University, Queensland, 4222, Australia d Institute of Marine Sciences, University of North Carolina, Chapel Hill, Morehead City, NC, 28557, USA e Department of Ecology, Evolution and Natural Resources Rutgers, The State University of New Jersey, USA f Centre for Integrative Ecology, School of Life and Environmental Sciences, Deakin University, Burwood, VIC, 3125, Australia g Departamento de Oceanografia Biologica, Instituto Oceanografico, Universidade de Sao~ Paulo, Praça do Oceanografico, 191, CEP 05508-120, Sao~ Paulo, SP, Brazil h Centre for Marine Ecosystems Research, Edith Cowan University, WA, Australia article info abstract Article history: Beach and coastal dune systems are increasingly subjected to a broad range of anthropogenic pressures Received 23 October 2015 that on many shorelines require significant conservation and mitigation interventions. -
Temporal Distribution in the Abundance of the Fiddler Crab Uca (Leptuca) Uruguayensis Nobili, 1901 (Decapoda: Ocypodidae) from G
Nauplius 21(2): 151-159, 2013 151 Temporal distribution in the abundance of the fiddler crab Uca (Leptuca) uruguayensis Nobili, 1901 (Decapoda: Ocypodidae) from Garças River mangrove, Guaratuba Bay, southern Brazil Salise Brandt Martins and Setuko Masunari (SBM, SM) Department of Zoology, Institute of Biological Sciences, Federal University of Paraná. Centro Politécnico, Jardim das Américas, Caixa Postal 19020, 81531-980, Curitiba, Paraná, Brazil. E-mails: (SBM) [email protected]; (SM) [email protected] ABSTRACT - A study on the temporal distribution, sex ratio, reproductive period, recruitment of juveniles and size composition of individuals of the fiddler crab Uca (Leptuca) uruguayensis was carried out in a population living in the Garças River mangrove, Guaratuba Bay, Paraná State, Brazil. Eight square samples of 0.25 m² (0.50 m side) were obtained on a monthly basis, from April/2011 to March/2012. The crabs were collected through the excavation of burrows and their carapace width (CW) was measured. Air and water temperatures varied from 19.0 to 29.5°C and 17.0 to 27.0°C, respectively, the salinity from 7 to 23 and the soil temperature from 19.0 to 29.2°C. A total of 1,099 fiddler crabs were collected, being 529 males, 520 females (of these, 9 ovigerous) and 50 sexually undifferentiated individuals. The average density of the population ranged from 12 (June/11) to 71 ind.m-² (May/11), but its annual fluctuation was not correlated to abiotic variables. The sex ratio was 1:1 all year round and in all CW classes. Although in low abundance, ovigerous females were recorded in six months and juvenile crabs were present all year round, indicating a continuous reproduction and recruitment of the species.