Notes on Indo-West Pacific Crustacea Decapoda III to IX
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A Classification of Living and Fossil Genera of Decapod Crustaceans
RAFFLES BULLETIN OF ZOOLOGY 2009 Supplement No. 21: 1–109 Date of Publication: 15 Sep.2009 © National University of Singapore A CLASSIFICATION OF LIVING AND FOSSIL GENERA OF DECAPOD CRUSTACEANS Sammy De Grave1, N. Dean Pentcheff 2, Shane T. Ahyong3, Tin-Yam Chan4, Keith A. Crandall5, Peter C. Dworschak6, Darryl L. Felder7, Rodney M. Feldmann8, Charles H. J. M. Fransen9, Laura Y. D. Goulding1, Rafael Lemaitre10, Martyn E. Y. Low11, Joel W. Martin2, Peter K. L. Ng11, Carrie E. Schweitzer12, S. H. Tan11, Dale Tshudy13, Regina Wetzer2 1Oxford University Museum of Natural History, Parks Road, Oxford, OX1 3PW, United Kingdom [email protected] [email protected] 2Natural History Museum of Los Angeles County, 900 Exposition Blvd., Los Angeles, CA 90007 United States of America [email protected] [email protected] [email protected] 3Marine Biodiversity and Biosecurity, NIWA, Private Bag 14901, Kilbirnie Wellington, New Zealand [email protected] 4Institute of Marine Biology, National Taiwan Ocean University, Keelung 20224, Taiwan, Republic of China [email protected] 5Department of Biology and Monte L. Bean Life Science Museum, Brigham Young University, Provo, UT 84602 United States of America [email protected] 6Dritte Zoologische Abteilung, Naturhistorisches Museum, Wien, Austria [email protected] 7Department of Biology, University of Louisiana, Lafayette, LA 70504 United States of America [email protected] 8Department of Geology, Kent State University, Kent, OH 44242 United States of America [email protected] 9Nationaal Natuurhistorisch Museum, P. O. Box 9517, 2300 RA Leiden, The Netherlands [email protected] 10Invertebrate Zoology, Smithsonian Institution, National Museum of Natural History, 10th and Constitution Avenue, Washington, DC 20560 United States of America [email protected] 11Department of Biological Sciences, National University of Singapore, Science Drive 4, Singapore 117543 [email protected] [email protected] [email protected] 12Department of Geology, Kent State University Stark Campus, 6000 Frank Ave. -
Redalyc.Larval Development of the Rock Shrimp Rhynchocinetes Typus
Revista Chilena de Historia Natural ISSN: 0716-078X [email protected] Sociedad de Biología de Chile Chile DUPRÉ, ENRIQUE; FLORES, LUIS; PALMA, SERGIO Larval development of the rock shrimp Rhynchocinetes typus Milne Edwards, 1937 (Decapoda, Caridea) reared in the laboratory Revista Chilena de Historia Natural, vol. 81, núm. 2, 2008, pp. 155-170 Sociedad de Biología de Chile Santiago, Chile Available in: http://www.redalyc.org/articulo.oa?id=369944286001 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative LARVAL DEVELOPMENT OF RHYNCHOCINETES TYPUSRevista Chilena de Historia Natural155 81: 155-170, 2008 Larval development of the rock shrimp Rhynchocinetes typus Milne Edwards, 1937 (Decapoda, Caridea) reared in the laboratory Desarrollo larval del camarón de roca Rhynchocinetes typus Milne Edwards, 1937 (Decapoda, Caridea) cultivados en laboratorio ENRIQUE DUPRÉ1*, LUIS FLORES1 & SERGIO PALMA2 1 Departamento de Biología Marina, Facultad de Ciencias del Mar, Universidad Católica del Norte, Casilla117 Coquimbo, Chile; [email protected] 2 Escuela de Ciencias del Mar, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile *e-mail for correspondence: [email protected] ABSTRACT The first description of the larval stages of a representative of the family Rhynchocinetidae from the southeastern Pacific coast of South America is presented. Larvae of the rock shrimp Rhynchocinetes typus, from rocky subtidal environment of the Chile-Peru coast were reared in the laboratory at 22 ºC, salinity 32 and feeding with Artemia franciscana. Seven zoeal stages, which occur through 10 successive moults, are described and illustrated in detail. -
New Records of Marine Ornamental Shrimps (Decapoda: Stenopodidea and Caridea) from the Gulf of Mannar, Tamil Nadu, India
12 6 2010 the journal of biodiversity data 7 December 2016 Check List NOTES ON GEOGRAPHIC DISTRIBUTION Check List 12(6): 2010, 7 December 2016 doi: http://dx.doi.org/10.15560/12.6.2010 ISSN 1809-127X © 2016 Check List and Authors New records of marine ornamental shrimps (Decapoda: Stenopodidea and Caridea) from the Gulf of Mannar, Tamil Nadu, India Sanjeevi Prakash1, 3, Thipramalai Thangappan Ajith Kumar2* and Thanumalaya Subramoniam1 1 Centre for Climate Change Studies, Sathyabama University, Jeppiaar Nagar, Rajiv Gandhi Salai, Chennai - 600119, Tamil Nadu, India 2 ICAR - National Bureau of Fish Genetic Resources, Canal Ring Road, Dilkusha Post, Lucknow - 226002, Uttar Pradesh, India 3 Current address: Department of Biological Sciences, Clemson University, Clemson, SC 29634, USA * Corresponding author. E-mail: [email protected] Abstract: Marine ornamental shrimps found in from coral reefs have greatly affected their diversity and tropical coral reef waters are widely recognized for the distribution (Wabnitz et al. 2003). aquarium trade. Our survey of ornamental shrimps in Among all the ornamental shrimps, Stenopus the Gulf of Mannar, Tamil Nadu (India) has found three spp. and Lysmata spp. are the most attractive and species, which we identify as Stenopus hispidus Olivier, extensively traded organisms in the marine aquarium 1811, Lysmata debelius Bruce, 1983, and L. amboinensis industry (Calado 2008). Interestingly, these shrimps are De Man, 1888, based on morphology and color pattern. associates of fishes, in particular, the groupers and giant These shrimps are recorded for the first time in Gulf of moray eels (Gymnothorax spp.). These shrimps display a Mannar, Tamil Nadu. -
Review on the Genuscinetorhynchus Holthuis, 1995 from the Indo-West
Or. Chctce, : (JOitt Tn®/ S^/wtr H7' 2 Crustacea Decapoda: Review on the genus Cinetorhynchus Holthuis, 1995 from the Indo-West Pacific (Caridea: Rhynchocinetidae) JUNJIOKUNO Natural History Museum and Institute, Chiba, 955-2 Aoba-cho, Chuo-ku, Chiba, 260, Japan ABSTRACT Cinetorhynchus Holthuis, 1995 established as a subgenus of the genus Rhynchocinetes H. Milne Edwards, 1837, is elevated to the generic rank. In addition to the definitions pointed out by HOLTHUIS (1995), this genus is distinguished from the type genus by having two rows of spines on the ischia and rneri of the third to fifth pereiopods. Cinetorhynchus is composed of C. rigens (Gordon, 1936), the type species, from the Madeira Islands, eastern Atlantic, and the following six species from the Indo-West Pacific : C. concolor (Okuno, 1994), C. erythrostictus sp. nov., C. hendersoni (Kemp, 1925), G hiatti (Holthuis & Hayashi, 1967), C. reticulum sp. nov. and C. striatus (Nomura & Hayashi, 1992). The key for the morphological characters and the color photographs of the live-coloration of each species are provided for the identification of the species. INTRODUCTION The caridean family Rhynchocinetidae has been composed of the single genus, Rhynchocinetes H. Milne Edwards, 1837 (HOLTHUIS, 1993), which contains 15 species. Most shrimps are inhabitant of tropical to temperate reefs, and commonly known as hinge-beak shrimp in having the typically movable rostrum which is articulated with the carapace. Recently, the rhynchocinetid shrimps were clearly divided into two subgenera based on the following morphological characters (HOLTHUIS, 1995). The subgenus Rhynchocinetes has two acute teeth at median carina of carapace behind the distinct rostral articulation, a supraorbital spine and no spine on the posterolateral margins of fourth and fifth abdominal somites, whereas the subgenus Cinetorhynchus Holthuis, 1995 has three teeth at OKUNO, J., 1997 — Crustacea Decapoda : Review on the genus Cinetorhynchus Holthuis, 1995 from the Indo-West Pacific (Caridea : Rhynchocinetidae). -
Benvenuto, C and SC Weeks. 2020
--- Not for reuse or distribution --- 8 HERMAPHRODITISM AND GONOCHORISM Chiara Benvenuto and Stephen C. Weeks Abstract This chapter compares two sexual systems: hermaphroditism (each individual can produce gametes of either sex) and gonochorism (each individual produces gametes of only one of the two distinct sexes) in crustaceans. These two main sexual systems contain a variety of alternative modes of reproduction, which are of great interest from applied and theoretical perspectives. The chapter focuses on the description, prevalence, analysis, and interpretation of these sexual systems, centering on their evolutionary transitions. The ecological correlates of each reproduc- tive system are also explored. In particular, the prevalence of “unusual” (non- gonochoristic) re- productive strategies has been identified under low population densities and in unpredictable/ unstable environments, often linked to specific habitats or lifestyles (such as parasitism) and in colonizing species. Finally, population- level consequences of some sexual systems are consid- ered, especially in terms of sex ratios. The chapter aims to provide a broad and extensive overview of the evolution, adaptation, ecological constraints, and implications of the various reproductive modes in this extraordinarily successful group of organisms. INTRODUCTION 1 Historical Overview of the Study of Crustacean Reproduction Crustaceans are a very large and extraordinarily diverse group of mainly aquatic organisms, which play important roles in many ecosystems and are economically important. Thus, it is not surprising that numerous studies focus on their reproductive biology. However, these reviews mainly target specific groups such as decapods (Sagi et al. 1997, Chiba 2007, Mente 2008, Asakura 2009), caridean Reproductive Biology. Edited by Rickey D. Cothran and Martin Thiel. -
Cinetorhynchus Manningi, a New Shrimp (Crustacea: Decapoda: Caridea: Rhynchocinetidae) from the Western Atlantic
23 December 1996 PROCEEDINGS OF THE BIOLOGICAL SOCIETY OF WASHINGTON 109(4):725-730. 1996 Cinetorhynchus manningi, a new shrimp (Crustacea: Decapoda: Caridea: Rhynchocinetidae) from the western Atlantic Junji Okuno Natural History Museum and Institute, Chiba, 955-2 Aoba-cho, Chuo-ku, Chiba 260, Japan Abstract.—A new rhynchocinetid shrimp, Cinetorhynchus manningi, is de- scribed and illustrated based on two ovigerous female specimens from the western Atlantic Ocean. The new species is readily distinguished from the other seven congeners by the absence of arthrobranchs on the second and third per- eiopods, and constitutes the second rhynchocinetid from the Atlantic ocean. Shrimps of the family Rhynchocinetidae ural History, Smithsonian Institution, differ from other caridean shrimps by hav- Washington, D.C. ing a typically movable rostrum, fine trans- verse striae on the surfaces of the carapace Cinetorhynchus manningi, new species and abdominal somites, first two pairs of Figs. 1, 2 pereiopods robust, fingers bearing long lat- Rhynchocinetes rigens.—Manning, 1961:1 eral and terminal spines, and second pereio- (in part) (not Rhynchocinetes rigens Gor- pod with carpus entire, not subdivided. Hol- don, 1936). thuis (1995) divided the genus Rhynchoci- Material.—Caribbean Sea: USNM netes s.l. into two subgenera, Rhynchoci- 277772, holotype, ovigerous female, 8.5 netes H. Milne-Edwards, 1837 and Cineto- mm CL, Virgin Islands, Eagle Shoal, 10.5 rhynchus Holthuis, 1995. Okuno (in press) m, 1 Feb 1961; USNM 277773, paratype, elevated these subgenera to generic rank, ovigerous female, 8.0 mm CL, Florida, off and included in Cinetorhynchus six species Elliot Key, Bache Shoals, 4.5 m, 4 May from the Indo-Pacific and one from the At- 1960, coll. -
Marine Biodiversity in India
MARINEMARINE BIODIVERSITYBIODIVERSITY ININ INDIAINDIA MARINE BIODIVERSITY IN INDIA Venkataraman K, Raghunathan C, Raghuraman R, Sreeraj CR Zoological Survey of India CITATION Venkataraman K, Raghunathan C, Raghuraman R, Sreeraj CR; 2012. Marine Biodiversity : 1-164 (Published by the Director, Zool. Surv. India, Kolkata) Published : May, 2012 ISBN 978-81-8171-307-0 © Govt. of India, 2012 Printing of Publication Supported by NBA Published at the Publication Division by the Director, Zoological Survey of India, M-Block, New Alipore, Kolkata-700 053 Printed at Calcutta Repro Graphics, Kolkata-700 006. ht³[eg siJ rJrJ";t Œtr"fUhK NATIONAL BIODIVERSITY AUTHORITY Cth;Govt. ofmhfUth India ztp. ctÖtf]UíK rvmwvtxe yÆgG Dr. Balakrishna Pisupati Chairman FOREWORD The marine ecosystem is home to the richest and most diverse faunal and floral communities. India has a coastline of 8,118 km, with an exclusive economic zone (EEZ) of 2.02 million sq km and a continental shelf area of 468,000 sq km, spread across 10 coastal States and seven Union Territories, including the islands of Andaman and Nicobar and Lakshadweep. Indian coastal waters are extremely diverse attributing to the geomorphologic and climatic variations along the coast. The coastal and marine habitat includes near shore, gulf waters, creeks, tidal flats, mud flats, coastal dunes, mangroves, marshes, wetlands, seaweed and seagrass beds, deltaic plains, estuaries, lagoons and coral reefs. There are four major coral reef areas in India-along the coasts of the Andaman and Nicobar group of islands, the Lakshadweep group of islands, the Gulf of Mannar and the Gulf of Kachchh . The Andaman and Nicobar group is the richest in terms of diversity. -
Periclimenes Paivai on the Scyphozoan Jellyfsh Lychnorhiza Lucerna: Probing for Territoriality and Inferring Its Mating System J
Baeza et al. Helgol Mar Res (2017) 71:17 DOI 10.1186/s10152-017-0497-8 Helgoland Marine Research ORIGINAL ARTICLE Open Access Host‑use pattern of the shrimp Periclimenes paivai on the scyphozoan jellyfsh Lychnorhiza lucerna: probing for territoriality and inferring its mating system J. Antonio Baeza1,2,3*, Samara de Paiva Barros‑Alves4,5, Rudá Amorim Lucena6, Silvio Felipe Barbosa Lima7,8 and Douglas Fernandes Rodrigues Alves4,5 Abstract In symbiotic crustaceans, host-use patterns vary broadly. Some species inhabit host individuals solitarily, other spe‑ cies live in heterosexual pairs, and even other species live in aggregations. This disparity in host-use patterns coupled with considerable diferences in host ecology provide opportunities to explore how environmental conditions afect animal behavior. In this study, we explored whether or not symbiotic crustaceans inhabiting relatively large and structurally complex host species live in aggregations. We expected Periclimenes paivai, a small caridean shrimp that lives among the tentacles of the large and morphologically complex scyphozoan jellyfsh Lychnorhiza lucerna, to live in groups given that the host traits above constraint host-monopolization behaviors by symbiotic crustaceans. We described the population distribution of P. paivai during a bloom of L. lucerna near the mouth of the Paraíba River estuary in Paraíba, Brazil. The population distribution of P. paivai did not difer statistically from a random Poisson dis‑ tribution. Male shrimps were most often found dwelling on the surface of L. lucerna individuals as small groups (2–4 individuals), in agreement with expectations. Periclimenes paivai is a sexually dimorphic species with males attaining smaller average body sizes than females and exhibiting no elaborated weaponry (claws). -
Inferences on Mating and Sexual Systems of Two
A peer-reviewed open-access journal ZooKeys 457:Inferences 187–209 (2014) on mating and sexual systems of two PacificCinetorhynchus shrimps... 187 doi: 10.3897/zookeys.457.6512 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry Raymond T. Bauer1, Junji Okuno2, Martin Thiel3 1 Department of Biology, University of Louisiana, Lafayette, Louisiana 70504-2451, USA 2 Coastal Branch of Natural History Museum and Institute, Chiba, 123 Yoshio, Katsuura, Chiba 299-5242, Japan 3 Facultad de Ciencias del Mar, Universidad Católica del Norte, Larrondo 1281, Coquimbo, Chile Corresponding author: Raymond T. Bauer ([email protected]) Academic editor: I.S. Wehrtmann | Received 28 October 2013 | Accepted 21 May 2014 | Published 25 November 2014 http://zoobank.org/540E3608-256A-45DB-ABFB-919D97E8E181 Citation: Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda: Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 187–209. doi: 10.3897/zookeys.457.6512 Abstract Sexual dimorphism in body size and weaponry was examined in two Cinetorhynchus shrimp species in or- der to formulate hypotheses on their sexual and mating systems. Collections of C. sp. A and C. sp. B were made in March, 2011 on Coconut Island, Hawaii, by hand dipnetting and minnow traps in coral rubble bottom in shallow water. -
Effects of Predation on Diel Activity and Habitat Use of the Coral- Reef Shrimp Cinetorhynchus Hendersoni (Rhynchocinetidae)
Coral Reefs (2014) 33:639–650 DOI 10.1007/s00338-014-1163-0 REPORT Effects of predation on diel activity and habitat use of the coral- reef shrimp Cinetorhynchus hendersoni (Rhynchocinetidae) Nicolas C. Ory • David Dudgeon • Nicolas Duprey • Martin Thiel Received: 3 January 2014 / Accepted: 29 April 2014 / Published online: 17 May 2014 Ó Springer-Verlag Berlin Heidelberg 2014 Abstract Nonlethal effects of predators on prey behav- on the reef; complex substrata were preferred, while simple iour are still poorly understood, although they may have substrata were avoided. Shrimps were abundant on high- cascading effects through food webs. Underwater obser- complexity columnar–foliate Porites rus, but tended to vations and experiments were conducted on a shallow make little use of branching Acropora spp. Subsequent fringing coral reef in Malaysia to examine whether pre- tethering experiments, conducted during daytime in June dation risks affect diel activity, habitat use, and survival of 2013, compared the relative mortality of shrimps on simple the rhynchocinetid shrimp Cinetorhynchus hendersoni. The (sand–rubble, massive Porites spp.) and complex (P. rus, study site was within a protected area where predatory fish branching Acropora spp.) substrata under different preda- were abundant. Visual surveys and tethering experiments tion risk scenarios (i.e., different tether lengths and expo- were conducted in April–May 2010 to compare the abun- sure durations). The mortality of shrimps with short tethers dance of shrimps and predatory fishes and the relative (high risk) was high on all substrata while, under low and predation intensity on shrimps during day and night. intermediate predation risks (long tethers), shrimp mortal- Shrimps were not seen during the day but came out of ity was reduced on complex corals relative to that on sand– refuges at night, when the risk of being eaten was reduced. -
Decapoda (Crustacea) of the Gulf of Mexico, with Comments on the Amphionidacea
•59 Decapoda (Crustacea) of the Gulf of Mexico, with Comments on the Amphionidacea Darryl L. Felder, Fernando Álvarez, Joseph W. Goy, and Rafael Lemaitre The decapod crustaceans are primarily marine in terms of abundance and diversity, although they include a variety of well- known freshwater and even some semiterrestrial forms. Some species move between marine and freshwater environments, and large populations thrive in oligohaline estuaries of the Gulf of Mexico (GMx). Yet the group also ranges in abundance onto continental shelves, slopes, and even the deepest basin floors in this and other ocean envi- ronments. Especially diverse are the decapod crustacean assemblages of tropical shallow waters, including those of seagrass beds, shell or rubble substrates, and hard sub- strates such as coral reefs. They may live burrowed within varied substrates, wander over the surfaces, or live in some Decapoda. After Faxon 1895. special association with diverse bottom features and host biota. Yet others specialize in exploiting the water column ment in the closely related order Euphausiacea, treated in a itself. Commonly known as the shrimps, hermit crabs, separate chapter of this volume, in which the overall body mole crabs, porcelain crabs, squat lobsters, mud shrimps, plan is otherwise also very shrimplike and all 8 pairs of lobsters, crayfish, and true crabs, this group encompasses thoracic legs are pretty much alike in general shape. It also a number of familiar large or commercially important differs from a peculiar arrangement in the monospecific species, though these are markedly outnumbered by small order Amphionidacea, in which an expanded, semimem- cryptic forms. branous carapace extends to totally enclose the compara- The name “deca- poda” (= 10 legs) originates from the tively small thoracic legs, but one of several features sepa- usually conspicuously differentiated posteriormost 5 pairs rating this group from decapods (Williamson 1973). -
Diversity and Abundance of Conspicuous Macrocrustaceans on Coral Reefs Differing in Level of Degradation
Diversity and abundance of conspicuous macrocrustaceans on coral reefs differing in level of degradation Roberto González-Gómez1,2, Patricia Briones-Fourzán1, Lorenzo Álvarez-Filip1 and Enrique Lozano-Álvarez1 1 Instituto de Ciencias del Mar y Limnología, Unidad Académica de Sistemas Arrecifales, Universidad Nacional Autónoma de México, Puerto Morelos, Quintana Roo, Mexico 2 Posgrado en Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México, Mexico, Ciudad de México, Mexico ABSTRACT Coral reefs sustain abundant and diverse macrocrustaceans that perform multiple ecological roles, but coral reefs are undergoing massive degradation that may be driving changes in the species composition and abundance of reef-associated macrocrustaceans. To provide insight into this issue, we used non-destructive visual census techniques to compare the diversity and abundance of conspicuous macrocrustaceans (i.e., those >1 cm and visible without disturbance) between two shallow Caribbean coral reefs similar in size (∼1.5 km in length) and close to each other, but one (``Limones'') characterized by extensive stands of the branching coral Acropora palmata, and the other (``Bonanza'') dominated by macroalgae and relic coral skeletons and rubble (i.e., degraded). We also assessed the structural complexity of each reef and the percent cover of various benthic community components. Given the type of growth of A. palmata, we expected to find a greater structural complexity, a higher cover of live coral, and a lower cover of macroalgae on Limones,