Squillites Spinosus (Syncarida, Malacostraca)
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Decapod Crustacean Grooming: Functional Morphology, Adaptive Value, and Phylogenetic Significance
Decapod crustacean grooming: Functional morphology, adaptive value, and phylogenetic significance N RAYMOND T.BAUER Center for Crustacean Research, University of Southwestern Louisiana, USA ABSTRACT Grooming behavior is well developed in many decapod crustaceans. Antennular grooming by the third maxillipedes is found throughout the Decapoda. Gill cleaning mechanisms are qaite variable: chelipede brushes, setiferous epipods, epipod-setobranch systems. However, microstructure of gill cleaning setae, which are equipped with digitate scale setules, is quite conservative. General body grooming, performed by serrate setal brushes on chelipedes and/or posterior pereiopods, is best developed in decapods at a natant grade of body morphology. Brachyuran crabs exhibit less body grooming and virtually no specialized body grooming structures. It is hypothesized that the fouling pressures for body grooming are more severe in natant than in replant decapods. Epizoic fouling, particularly microbial fouling, and sediment fouling have been shown r I m ans of amputation experiments to produce severe effects on olfactory hairs, gills, and i.icubated embryos within short lime periods. Grooming has been strongly suggested as an important factor in the coevolution of a rhizocephalan parasite and its anomuran host. The behavioral organization of grooming is poorly studied; the nature of stimuli promoting grooming is not understood. Grooming characters may contribute to an understanding of certain aspects of decapod phylogeny. The occurrence of specialized antennal grooming brushes in the Stenopodidea, Caridea, and Dendrobranchiata is probably not due to convergence; alternative hypotheses are proposed to explain the distribution of this grooming character. Gill cleaning and general body grooming characters support a thalassinidean origin of the Anomura; the hypothesis of brachyuran monophyly is supported by the conservative and unique gill-cleaning method of the group. -
Horseshoe Crab Limulus Polyphemus
Supplemental Volume: Species of Conservation Concern SC SWAP 2015 Atlantic Horseshoe Crab Limulus polyphemus Contributor (2005): Elizabeth Wenner (SCDNR) Reviewed and Edited (2013): Larry Delancey and Peter Kingsley-Smith [SCDNR] DESCRITPION Taxonomy and Basic Description Despite their name, horseshoe crabs are not true crabs. The Atlantic horseshoe crab, Limulus polyphemus, is the only member of the Arthropoda subclass Xiphosura found in the Atlantic. Unlike true crabs, which have 2 pairs of antennae, a pair of jaws and 5pairs of legs, horseshoe crabs lack antennae and jaws and have 7 pairs of legs, including a pair of chelicerae. Chelicerae are appendages similar to those used by spiders and scorpions for grasping and crushing. In addition, horseshoe crabs have book lungs, similar to spiders and different from crabs, which have gills. Thus, horseshoe crabs are more closely related to spiders and scorpions than they are to other crabs. Their carapace is divided into three sections: the anterior portion is the prosoma; the middle section is the opithosoma; and the “tail” is called the telson. Horseshoe crabs have two pairs of eyes located on the prosoma, one anterior set of simple eyes, and one set of lateral compound eyes similar to those of insects. In addition, they possess a series of photoreceptors on the opithosoma and telson (Shuster 1982). Horseshoe crabs are long-lived animals. After attaining sexual maturity at 9 to 12 years of age, they may live for another 10 years or more. Like other arthropods, horseshoe crabs must molt in order to grow. As the horseshoe crab ages, more and more time passes between molts, with 16 to 19 molts occurring before a crab becomes mature, stops growing, and switches energy expenditure to reproduction. -
Biochemical Divergence Between Cavernicolous and Marine
The position of crustaceans within Arthropoda - Evidence from nine molecular loci and morphology GONZALO GIRIBET', STEFAN RICHTER2, GREGORY D. EDGECOMBE3 & WARD C. WHEELER4 Department of Organismic and Evolutionary- Biology, Museum of Comparative Zoology; Harvard University, Cambridge, Massachusetts, U.S.A. ' Friedrich-Schiller-UniversitdtJena, Instituifiir Spezielte Zoologie und Evolutionsbiologie, Jena, Germany 3Australian Museum, Sydney, NSW, Australia Division of Invertebrate Zoology, American Museum of Natural History, New York, U.S.A. ABSTRACT The monophyly of Crustacea, relationships of crustaceans to other arthropods, and internal phylogeny of Crustacea are appraised via parsimony analysis in a total evidence frame work. Data include sequences from three nuclear ribosomal genes, four nuclear coding genes, and two mitochondrial genes, together with 352 characters from external morphol ogy, internal anatomy, development, and mitochondrial gene order. Subjecting the com bined data set to 20 different parameter sets for variable gap and transversion costs, crusta ceans group with hexapods in Tetraconata across nearly all explored parameter space, and are members of a monophyletic Mandibulata across much of the parameter space. Crustacea is non-monophyletic at low indel costs, but monophyly is favored at higher indel costs, at which morphology exerts a greater influence. The most stable higher-level crusta cean groupings are Malacostraca, Branchiopoda, Branchiura + Pentastomida, and an ostracod-cirripede group. For combined data, the Thoracopoda and Maxillopoda concepts are unsupported, and Entomostraca is only retrieved under parameter sets of low congruence. Most of the current disagreement over deep divisions in Arthropoda (e.g., Mandibulata versus Paradoxopoda or Cormogonida versus Chelicerata) can be viewed as uncertainty regarding the position of the root in the arthropod cladogram rather than as fundamental topological disagreement as supported in earlier studies (e.g., Schizoramia versus Mandibulata or Atelocerata versus Tetraconata). -
SPIRULA - Speciale Uitgave, Supplement Nr
SPIRULA - Speciale uitgave, supplement nr. 2 13 Eponiemen betreffende personen verbonden aan de NMV Gijs+C. Kronenberg Inleiding In het kader van het 50-jarig jubileum van de NMV werd een lijst gepubliceerd (KUIPER, 1984: 1589-1590) met In eponiemen, dat wil zeggen, weekdiersoortenvernoemd naar Nederlandse malacologen. latere jaren verschenen hierop een aantal aanvullingen (KUIPER, 1986; KUIPER, 1988; KUIPER, 1989; KUIPER, 1991; KUIPER, 1992; KUIPER, 1993; KUIPER 1995). Na 1995 zijn er verder geen overzichten meer samengesteld. Helaas is aan het initiatiefvan met KUIPER (opera cit.) geen vervolg gegeven, zodat we een achterstand zitten, maar die nu wordt weggewerkt middels deze vernieuwde lijst. Criteria perd door [KRONENBERG] (2001). Om in de lijst opgenomen te worden dientte worden voldaan Daarnaast hebben deze criteriaook als gevolg dat de namen aan drie criteria: Trochus wilsi PICKERY, 1989 (KUIPER 1992); Ischnochiton Men moet lid zijn (geweest) van de N.M.V. ofeen plaatselij- vanbellei KAAS; en Notoplax richardi KAAS [ook vernoemd ke schelpenwerkgroep enigszins geliëerd aan de NMV, of naar de heer R.A. VAN BELLE] (KUIPER, 1993) uitde lijst zijn daar in zeer nauwe (privé) relatie mee staan (huwelijk, geschrapt daar deze personen niet de Nederlandse nationali- dank samenwonen, kinderen) als voor de vele jaren trouwe teit (gehad) hebben, en taxa vernoemd naar Prof. Dr. J.K.L. Of in niet daar deze ondersteuning en dergelijke. men moet dusdanige pro- MARTIN opgenomen zijn niet de Nederlandse fessioneel malacologische relatie hebben gestaan dat de nationaliteitheeft gehad. auteur het taxon dat tot wilde in het Taxa beschreven door b.v. uit van uiting brengen ver- E.J. -
Amphibious Fishes: Terrestrial Locomotion, Performance, Orientation, and Behaviors from an Applied Perspective by Noah R
AMPHIBIOUS FISHES: TERRESTRIAL LOCOMOTION, PERFORMANCE, ORIENTATION, AND BEHAVIORS FROM AN APPLIED PERSPECTIVE BY NOAH R. BRESSMAN A Dissertation Submitted to the Graduate Faculty of WAKE FOREST UNIVESITY GRADUATE SCHOOL OF ARTS AND SCIENCES in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY Biology May 2020 Winston-Salem, North Carolina Approved By: Miriam A. Ashley-Ross, Ph.D., Advisor Alice C. Gibb, Ph.D., Chair T. Michael Anderson, Ph.D. Bill Conner, Ph.D. Glen Mars, Ph.D. ACKNOWLEDGEMENTS I would like to thank my adviser Dr. Miriam Ashley-Ross for mentoring me and providing all of her support throughout my doctoral program. I would also like to thank the rest of my committee – Drs. T. Michael Anderson, Glen Marrs, Alice Gibb, and Bill Conner – for teaching me new skills and supporting me along the way. My dissertation research would not have been possible without the help of my collaborators, Drs. Jeff Hill, Joe Love, and Ben Perlman. Additionally, I am very appreciative of the many undergraduate and high school students who helped me collect and analyze data – Mark Simms, Tyler King, Caroline Horne, John Crumpler, John S. Gallen, Emily Lovern, Samir Lalani, Rob Sheppard, Cal Morrison, Imoh Udoh, Harrison McCamy, Laura Miron, and Amaya Pitts. I would like to thank my fellow graduate student labmates – Francesca Giammona, Dan O’Donnell, MC Regan, and Christine Vega – for their support and helping me flesh out ideas. I am appreciative of Dr. Ryan Earley, Dr. Bruce Turner, Allison Durland Donahou, Mary Groves, Tim Groves, Maryland Department of Natural Resources, UF Tropical Aquaculture Lab for providing fish, animal care, and lab space throughout my doctoral research. -
Syncarid Crustaceans from the Montceau Lagersta¨Tte
[Palaeontology, Vol. 49, Part 3, 2006, pp. 647–672] SYNCARID CRUSTACEANS FROM THE MONTCEAU LAGERSTA¨ TTE (UPPER CARBONIFEROUS; FRANCE) by VINCENT PERRIER*, JEAN VANNIER*, PATRICK R. RACHEBOEUF , SYLVAIN CHARBONNIER*, DOMINIQUE CHABARDà and DANIEL SOTTYà *Universite´ Claude Bernard Lyon 1, UMR 5125 PEPS ‘Pale´oenvironnements et Pale´obiosphe`re’, Campus scientifique de la Doua, Baˆtiment Ge´ode, 2 rue Raphae¨l Dubois, 69622 Villeurbanne, France; e-mails: [email protected]; [email protected] Universite´ de Bretagne Occidentale, UMR 6538 ‘Domaines Oce´aniques’ – Pale´ontologie, UFR Sciences et Techniques, 6 avenue Le Gorgeu, CS 93837, F-29238 Brest cedex 3, France; e-mail: [email protected] àMuse´e d’Histoire Naturelle d’Autun, 14 rue St-Antoine, 71400 Autun, France Typescript received 28 September 2004; accepted in revised form 17 May 2005 Abstract: Key aspects of the morphology, autecology, sys- suggest a relatively low level of locomotory activity. The tematics and taphonomy of the crustacean syncarids from field of vision may have been large and panoramic (stalked the Montceau Lagersta¨tte (Upper Carboniferous, Stephanian eyes). Rows of pores on 12 trunk segments are interpreted B; France) are presented. Palaeocaris secretanae is the most as possible sensory organs used for current detection. abundant faunal element of the Montceau biota and shows Females were brooding eggs (clusters of eggs preserved striking morphological similarities with Palaeocaris typus along anteroventral trunk). Microprobe analysis indicates from the Mazon Creek Lagersta¨tte (Westphalian D; Illinois, that siderite is the major component of the nodules. Four USA). Palaeocaris secretanae was a shrimp-like animal with events played a key-role in the three-dimensional preserva- a short head (no head shield), large mandibles, 14 trunk tion of syncarids: (1) rapid burial, (2) minimal decomposi- segments (the first one being reduced) and a fan-like caudal tion, (3) phosphatic mineralization shortly after the termination. -
Phylogenomic Resolution of Sea Spider Diversification Through Integration Of
bioRxiv preprint doi: https://doi.org/10.1101/2020.01.31.929612; this version posted February 2, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Phylogenomic resolution of sea spider diversification through integration of multiple data classes 1Jesús A. Ballesteros†, 1Emily V.W. Setton†, 1Carlos E. Santibáñez López†, 2Claudia P. Arango, 3Georg Brenneis, 4Saskia Brix, 5Esperanza Cano-Sánchez, 6Merai Dandouch, 6Geoffrey F. Dilly, 7Marc P. Eleaume, 1Guilherme Gainett, 8Cyril Gallut, 6Sean McAtee, 6Lauren McIntyre, 9Amy L. Moran, 6Randy Moran, 5Pablo J. López-González, 10Gerhard Scholtz, 6Clay Williamson, 11H. Arthur Woods, 12Ward C. Wheeler, 1Prashant P. Sharma* 1 Department of Integrative Biology, University of Wisconsin–Madison, Madison, WI, USA 2 Queensland Museum, Biodiversity Program, Brisbane, Australia 3 Zoologisches Institut und Museum, Cytologie und Evolutionsbiologie, Universität Greifswald, Greifswald, Germany 4 Senckenberg am Meer, German Centre for Marine Biodiversity Research (DZMB), c/o Biocenter Grindel (CeNak), Martin-Luther-King-Platz 3, Hamburg, Germany 5 Biodiversidad y Ecología Acuática, Departamento de Zoología, Facultad de Biología, Universidad de Sevilla, Sevilla, Spain 6 Department of Biology, California State University-Channel Islands, Camarillo, CA, USA 7 Départment Milieux et Peuplements Aquatiques, Muséum national d’Histoire naturelle, Paris, France 8 Institut de Systématique, Emvolution, Biodiversité (ISYEB), Sorbonne Université, CNRS, Concarneau, France 9 Department of Biology, University of Hawai’i at Mānoa, Honolulu, HI, USA Page 1 of 31 bioRxiv preprint doi: https://doi.org/10.1101/2020.01.31.929612; this version posted February 2, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. -
Hickman's Pygmy Mountain Shrimp (Allanaspides Hickmani) Is a Small, Shrimp-Like Crustacean Belonging to the Family Anaspididae
THREATENED SPECIES LISTING STATEMENT Hickman’s Pygmy Mountain Shrimp Allanaspides hickmani Swain Wilson and Ong 1971 Status Commonwealth Endangered Species Protection Act 1992 . .Not listed Tasmanian Threatened Species Protection Act 1995 . .Rare Description Hickman's pygmy mountain shrimp (Allanaspides hickmani) is a small, shrimp-like crustacean belonging to the family Anaspididae. This family contains three genera, Allanaspides, Anaspides and Paranaspides, all of which are restricted to Tasmania. Allanaspides species can be readily identified by the presence of a conspicuous transparent window on its back (dorsal window) and stalked eyes. The two species of Allanaspides (A. hickmani and A. helonomus) can be separated by the size, shape and colour of this window. Hickman's pygmy 6 mm mountain shrimp has a rectangular shaped dorsal window which covers most of the width of the dorsal surface Illustration: Karen Richards behind the head; the tissue below the dorsal window contains a bright red pigment. A. helonomus has a clear, oval-shaped dorsal window covering approximately half the width of the dorsal surface behind the head (Swain et al. 1970; Swain et al. 1971). Hickman's pygmy mountain shrimp has its eyes situated terminally on eyestalks and adult males attain a body length of 11.7 mm. A. helonomus has its eyes positioned laterally on the end of the eyestalks and is the slightly larger species, attaining a body length of 15 mm. A more detailed description of Hickman's pygmy mountain shrimp is provided by Swain et al. (1971). The life history of Hickman's pygmy mountain shrimp is poorly known and can only be inferred from what little information is available for A. -
Does Biogeography Have a Future in a Globalized World with Globalized Faunas?
Contributions to Zoology, 77 (2) 127-133 (2008) Does biogeography have a future in a globalized world with globalized faunas? Frederick R. Schram Burke Museum, University of Washington, Seattle, P.O. Box 1567, Langley, WA 98260, USA, [email protected] ton.edu Key words: Anaspidacea, Bathynellacea, globalization, historical biogeography, vicariance Abstract in the Great Lakes and it is said that a new invader species is identified every eight months. The toll on The study of biogeography was once a pillar of evolution the fisheries of the Great Lakes alone has been dev- science. Both Darwin and especially Wallace found great in- astating. Another example is San Francisco Bay, spiration from the consideration of animal distributions. where some 234 invasive species have been recorded However, what is to happen to this discipline in a time of global trade, mass movement of people and goods, and the up to the present day, i.e., something like 90% of the resulting globalization of the planet’s biota? Can we still aquatic population of the bay. Finally, the infamous hope to delve into the fine points of past geography as it af- Chinese mitten crab, Eriocheir sinensis, is conduct- fected animal and plant evolution? Maybe we can, but only ing an on-going assault on Chesapeake Bay, and the with careful study of life forms that suffer minimal affects effect on the native blue crab populations is already – at present – from globalization, viz., marginal faunas of being measured. In the United States, invading ar- quite inaccessible environments. Two examples taken from syncarid crustaceans illustrate this point. -
Crustaceans Topics in Biodiversity
Topics in Biodiversity The Encyclopedia of Life is an unprecedented effort to gather scientific knowledge about all life on earth- multimedia, information, facts, and more. Learn more at eol.org. Crustaceans Authors: Simone Nunes Brandão, Zoologisches Museum Hamburg Jen Hammock, National Museum of Natural History, Smithsonian Institution Frank Ferrari, National Museum of Natural History, Smithsonian Institution Photo credit: Blue Crab (Callinectes sapidus) by Jeremy Thorpe, Flickr: EOL Images. CC BY-NC-SA Defining the crustacean The Latin root, crustaceus, "having a crust or shell," really doesn’t entirely narrow it down to crustaceans. They belong to the phylum Arthropoda, as do insects, arachnids, and many other groups; all arthropods have hard exoskeletons or shells, segmented bodies, and jointed limbs. Crustaceans are usually distinguishable from the other arthropods in several important ways, chiefly: Biramous appendages. Most crustaceans have appendages or limbs that are split into two, usually segmented, branches. Both branches originate on the same proximal segment. Larvae. Early in development, most crustaceans go through a series of larval stages, the first being the nauplius larva, in which only a few limbs are present, near the front on the body; crustaceans add their more posterior limbs as they grow and develop further. The nauplius larva is unique to Crustacea. Eyes. The early larval stages of crustaceans have a single, simple, median eye composed of three similar, closely opposed parts. This larval eye, or “naupliar eye,” often disappears later in development, but on some crustaceans (e.g., the branchiopod Triops) it is retained even after the adult compound eyes have developed. In all copepod crustaceans, this larval eye is retained throughout their development as the 1 only eye, although the three similar parts may separate and each become associated with their own cuticular lens. -
Protection of Host Anemones by Snapping Shrimps: a Case for Symbiotic Mutualism?
Symbiosis DOI 10.1007/s13199-014-0289-8 Protection of host anemones by snapping shrimps: a case for symbiotic mutualism? AmberM.McCammon& W. Randy Brooks Received: 4 June 2014 /Accepted: 29 July 2014 # Springer Science+Business Media Dordrecht 2014 Abstract The sea anemone Bartholomea annulata is an eco- especially common in marine environments (Roughgarden logically important member of Caribbean coral reefs which host 1975; Poulin and Grutter 1996;Côté2000). Mutualism; a a variety of symbiotic crustacean associates. Crustacean type of symbiotic relationship in which both partners derive exosymbionts typically gain protection from predation by dwell- some benefit from the association, are also widespread across ing with anemones. Concurrently, some symbionts may provide taxa (Boucher et al. 1982). The benefit(s) of symbiont- protection to their host by defending against anemone predators mediated protection of host species from microbial disease, such as the predatory fireworm, Hermodice carunculata,which parasites, and predators is increasingly evident (Haine 2008). can severely damage or completely devour prey anemones. Protection mechanisms are diverse and include various sym- Herein we show through both field and laboratory studies that biont derived chemical defenses (Haine 2008) as well as anemones hosting the symbiotic alpheid shrimp Alpheus armatus maintenance behaviors (Heil and McKey 2003; Stier et al. are significantly less likely to sustain damage by H. carunculata 2012) and defensive social interactions (Glynn 1980; Brooks than anemones without this shrimp. Our results suggest that the and Gwaltney 1993; Heil and McKey 2003;McKeonetal. association between A. armatus and B. annulata, although com- 2012). Previous studies have demonstrated that some crusta- plex because of the numerous symbionts involved, may be closer ceans will actively defend host cnidarians in their natural to mutualism on the symbiotic continuum. -
A Review of Natural Values Within the 2013 Extension to the Tasmanian Wilderness World Heritage Area
A review of natural values within the 2013 extension to the Tasmanian Wilderness World Heritage Area Nature Conservation Report 2017/6 Department of Primary Industries, Parks, Water and Environment Hobart A review of natural values within the 2013 extension to the Tasmanian Wilderness World Heritage Area Jayne Balmer, Jason Bradbury, Karen Richards, Tim Rudman, Micah Visoiu, Shannon Troy and Naomi Lawrence. Department of Primary Industries, Parks, Water and Environment Nature Conservation Report 2017/6, September 2017 This report was prepared under the direction of the Department of Primary Industries, Parks, Water and Environment (World Heritage Program). Australian Government funds were contributed to the project through the World Heritage Area program. The views and opinions expressed in this report are those of the authors and do not necessarily reflect those of the Tasmanian or Australian Governments. ISSN 1441-0680 Copyright 2017 Crown in right of State of Tasmania Apart from fair dealing for the purposes of private study, research, criticism or review, as permitted under the Copyright act, no part may be reproduced by any means without permission from the Department of Primary Industries, Parks, Water and Environment. Published by Natural Values Conservation Branch Department of Primary Industries, Parks, Water and Environment GPO Box 44 Hobart, Tasmania, 7001 Front Cover Photograph of Eucalyptus regnans tall forest in the Styx Valley: Rob Blakers Cite as: Balmer, J., Bradbury, J., Richards, K., Rudman, T., Visoiu, M., Troy, S. and Lawrence, N. 2017. A review of natural values within the 2013 extension to the Tasmanian Wilderness World Heritage Area. Nature Conservation Report 2017/6, Department of Primary Industries, Parks, Water and Environment, Hobart.