2007-09 Tunicate Management Plan
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Colonial Tunicates: Species Guide
SPECIES IN DEPTH Colonial Tunicates Colonial Tunicates Tunicates are small marine filter feeder animals that have an inhalant siphon, which takes in water, and an exhalant siphon that expels water once it has trapped food particles. Tunicates get their name from the tough, nonliving tunic formed from a cellulose-like material of carbohydrates and proteins that surrounds their bodies. Their other name, sea squirts, comes from the fact that many species will shoot LambertGretchen water out of their bodies when disturbed. Massively lobate colony of Didemnum sp. A growing on a rope in Sausalito, in San Francisco Bay. A colony of tunicates is comprised of many tiny sea squirts called zooids. These INVASIVE SEA SQUIRTS individuals are arranged in groups called systems, which form interconnected Star sea squirts (Botryllus schlosseri) are so named because colonies. Systems of these filter feeders the systems arrange themselves in a star. Zooids are shaped share a common area for expelling water like ovals or teardrops and then group together in small instead of having individual excurrent circles of about 20 individuals. This species occurs in a wide siphons. Individuals and systems are all variety of colors: orange, yellow, red, white, purple, grayish encased in a matrix that is often clear and green, or black. The larvae each have eight papillae, or fleshy full of blood vessels. All ascidian tunicates projections that help them attach to a substrate. have a tadpole-like larva that swims for Chain sea squirts (Botryloides violaceus) have elongated, less than a day before attaching itself to circular systems. Each system can have dozens of zooids. -
Tadpole Consumption Is a Direct Threat to the Endangered Purple Frog, Nasikabatrachus Sahyadrensis
SALAMANDRA 51(3) 252–258 30 October 2015 CorrespondenceISSN 0036–3375 Correspondence Tadpole consumption is a direct threat to the endangered purple frog, Nasikabatrachus sahyadrensis Ashish Thomas & S. D. Biju Systematics Lab, Department of Environmental Studies, University of Delhi, Delhi 110 007, India Corresponding author: S. D. Biju, e-mail: [email protected] Manuscript received: 5 July 2014 Accepted: 30 December 2014 by Alexander Kupfer Amphibians across the world are suffering alarming popu- Southeast Asia have witnessed drastic population declines lation declines with nearly one third of the ca 7,300 species caused by overexploitation over the last couple of decades being threatened worldwide (Stuart et al. 2008, Wake & (Warkentin et al. 2008). Often, natural populations are Vredenburg 2008, IUCN 2014). Major factors attributed harvested without regard of the consequences or implica- to the decline include habitat destruction (Houlahan et tions of this practice on the dynamics or sustainability of al. 2000, Sodhi et al. 2008), chemical pollution (Ber ger the exploited populations (Getz & Haight 1989). When 1998), climate change (Adams 1999, Carpenter & Tur- the extent of exploitation is greater than the sustaining ca- ner 2000), diseases (McCallum 2007, Cushman 2006), pacity or turnover rate of a species, there is every possi- and invasive species (Boone & Bridges 2003). The West- bility that the species may become locally extinct, which ern Ghats of India, a global hotspot for amphibian diver- would subsequently have drastic ecological implications sity and endemism (Biju 2001, Biju & Bossuyt 2003), has in the particular region (Duffy 2002, Wright et al. 2006, more than 40% of its amphibian fauna threatened with ex- Carpenter et al. -
Sea Squirt Symbionts! Or What I Did on My Summer Vacation… Leah Blasiak 2011 Microbial Diversity Course
Sea Squirt Symbionts! Or what I did on my summer vacation… Leah Blasiak 2011 Microbial Diversity Course Abstract Microbial symbionts of tunicates (sea squirts) have been recognized for their capacity to produce novel bioactive compounds. However, little is known about most tunicate-associated microbial communities, even in the embryology model organism Ciona intestinalis. In this project I explored 3 local tunicate species (Ciona intestinalis, Molgula manhattensis, and Didemnum vexillum) to identify potential symbiotic bacteria. Tunicate-specific bacterial communities were observed for all three species and their tissue specific location was determined by CARD-FISH. Introduction Tunicates and other marine invertebrates are prolific sources of novel natural products for drug discovery (reviewed in Blunt, 2010). Many of these compounds are biosynthesized by a microbial symbiont of the animal, rather than produced by the animal itself (Schmidt, 2010). For example, the anti-cancer drug patellamide, originally isolated from the colonial ascidian Lissoclinum patella, is now known to be produced by an obligate cyanobacterial symbiont, Prochloron didemni (Schmidt, 2005). Research on such microbial symbionts has focused on their potential for overcoming the “supply problem.” Chemical synthesis of natural products is often challenging and expensive, and isolation of sufficient quantities of drug for clinical trials from wild sources may be impossible or environmentally costly. Culture of the microbial symbiont or heterologous expression of the biosynthetic genes offers a relatively economical solution. Although the microbial origin of many tunicate compounds is now well established, relatively little is known about the extent of such symbiotic associations in tunicates and their biological function. Tunicates (or sea squirts) present an interesting system in which to study bacterial/eukaryotic symbiosis as they are deep-branching members of the Phylum Chordata (Passamaneck, 2005 and Buchsbaum, 1948). -
What Do Tadpoles Really Eat? Assessing the Trophic Status of an Understudied and Imperiled Group of Consumers in Freshwater Habitats
Freshwater Biology (2007) 52, 386–395 doi:10.1111/j.1365-2427.2006.01694.x OPINION What do tadpoles really eat? Assessing the trophic status of an understudied and imperiled group of consumers in freshwater habitats RONALD ALTIG,* MATT R. WHILES† AND CINDY L. TAYLOR‡ *Department of Biological Sciences, Mississippi State University, Mississippi State, MS, U.S.A. †Department of Zoology and Center for Ecology, Southern Illinois University, Carbondale, IL, U.S.A. ‡Department of Biology, Austin Peay State University, Clarksville, TN, U.S.A. SUMMARY 1. Understanding the trophic status of consumers in freshwater habitats is central to understanding their ecological roles and significance. Tadpoles are a diverse and abundant component of many freshwater habitats, yet we know relatively little about their feeding ecology and true trophic status compared with many other consumer groups. While many tadpole species are labelled herbivores or detritivores, there is surprisingly little evidence to support these trophic assignments. 2. Here we discuss shortcomings in our knowledge of the feeding ecology and trophic status of tadpoles and provide suggestions and examples of how we can more accurately quantify their trophic status and ecological significance. 3. Given the catastrophic amphibian declines that are ongoing in many regions of the planet, there is a sense of urgency regarding this information. Understanding the varied ecological roles of tadpoles will allow for more effective conservation of remaining populations, benefit captive breeding programmes, and allow for more accurate predic- tions of the ecological consequences of their losses. Keywords: amphibian, assimilation, diet, feeding behaviour, omnivory Amphibians are disappearing from the planet at an of the functional roles and trophic status of general- alarming rate (Stuart et al., 2004; Lips et al., 2005). -
A New Species of the Genus Nasikabatrachus (Anura, Nasikabatrachidae) from the Eastern Slopes of the Western Ghats, India
Alytes, 2017, 34 (1¢4): 1¢19. A new species of the genus Nasikabatrachus (Anura, Nasikabatrachidae) from the eastern slopes of the Western Ghats, India S. Jegath Janani1,2, Karthikeyan Vasudevan1, Elizabeth Prendini3, Sushil Kumar Dutta4, Ramesh K. Aggarwal1* 1Centre for Cellular and Molecular Biology (CSIR-CCMB), Uppal Road, Tarnaka, Hyderabad, 500007, India. <[email protected]>, <[email protected]>. 2Current Address: 222A, 5th street, Annamalayar Colony, Sivakasi, 626123, India.<[email protected]>. 3Division of Vertebrate Zoology, Department of Herpetology, American Museum of Natural History, Central Park West at 79th Street, New York NY 10024-5192, USA. <[email protected]>. 4Nature Environment and Wildlife Society (NEWS), Nature House, Gaudasahi, Angul, Odisha. <[email protected]>. * Corresponding Author. We describe a new species of the endemic frog genus Nasikabatrachus,from the eastern slopes of the Western Ghats, in India. The new species is morphologically, acoustically and genetically distinct from N. sahyadrensis. Computed tomography scans of both species revealed diagnostic osteological differences, particularly in the vertebral column. Male advertisement call analysis also showed the two species to be distinct. A phenological difference in breeding season exists between the new species (which breeds during the northeast monsoon season; October to December), and its sister species (which breeds during the southwest monsoon; May to August). The new species shows 6 % genetic divergence (K2P) at mitochondrial 16S rRNA (1330 bp) partial gene from its congener, indicating clear differentiation within Nasikabatra- chus. Speciation within this fossorial lineage is hypothesized to have been caused by phenological shift in breeding during different monsoon seasons—the northeast monsoon in the new species versus southwest monsoon in N. -
Examples of Sea Sponges
Examples Of Sea Sponges Startling Amadeus burlesques her snobbishness so fully that Vaughan structured very cognisably. Freddy is ectypal and stenciling unsocially while epithelial Zippy forces and inflict. Monopolistic Porter sailplanes her honeymooners so incorruptibly that Sutton recirculates very thereon. True only on water leaves, sea of these are animals Yellow like Sponge Oceana. Deeper dives into different aspects of these glassy skeletons are ongoing according to. Sponges theoutershores. Cell types epidermal cells form outer covering amoeboid cells wander around make spicules. Check how These Beautiful Pictures of Different Types of. To be optimal for bathing, increasing with examples of brooding forms tan ct et al ratios derived from other microscopic plants from synthetic sponges belong to the university. What is those natural marine sponge? Different types of sponges come under different price points and loss different uses in. Global Diversity of Sponges Porifera NCBI NIH. Sponges EnchantedLearningcom. They publish the outer shape of rubber sponge 1 Some examples of sponges are Sea SpongeTube SpongeVase Sponge or Sponge Painted. Learn facts about the Porifera or Sea Sponges with our this Easy mountain for Kids. What claim a course Sponge Acme Sponge Company. BG Silicon isotopes of this sea sponges new insights into. Sponges come across an incredible summary of colors and an amazing array of shapes. 5 Fascinating Types of what Sponge Leisure Pro. Sea sponges often a tube-like bodies with his tiny pores. Sponges The World's Simplest Multi-Cellular Creatures. Sponges are food of various nudbranchs sea stars and fish. Examples of sponges Answers Answerscom. Sponges info and games Sheppard Software. -
The Origins of Chordate Larvae Donald I Williamson* Marine Biology, University of Liverpool, Liverpool L69 7ZB, United Kingdom
lopmen ve ta e l B Williamson, Cell Dev Biol 2012, 1:1 D io & l l o l g DOI: 10.4172/2168-9296.1000101 e y C Cell & Developmental Biology ISSN: 2168-9296 Research Article Open Access The Origins of Chordate Larvae Donald I Williamson* Marine Biology, University of Liverpool, Liverpool L69 7ZB, United Kingdom Abstract The larval transfer hypothesis states that larvae originated as adults in other taxa and their genomes were transferred by hybridization. It contests the view that larvae and corresponding adults evolved from common ancestors. The present paper reviews the life histories of chordates, and it interprets them in terms of the larval transfer hypothesis. It is the first paper to apply the hypothesis to craniates. I claim that the larvae of tunicates were acquired from adult larvaceans, the larvae of lampreys from adult cephalochordates, the larvae of lungfishes from adult craniate tadpoles, and the larvae of ray-finned fishes from other ray-finned fishes in different families. The occurrence of larvae in some fishes and their absence in others is correlated with reproductive behavior. Adult amphibians evolved from adult fishes, but larval amphibians did not evolve from either adult or larval fishes. I submit that [1] early amphibians had no larvae and that several families of urodeles and one subfamily of anurans have retained direct development, [2] the tadpole larvae of anurans and urodeles were acquired separately from different Mesozoic adult tadpoles, and [3] the post-tadpole larvae of salamanders were acquired from adults of other urodeles. Reptiles, birds and mammals probably evolved from amphibians that never acquired larvae. -
0041085-15082018101610.Pdf
Cronfa - Swansea University Open Access Repository _____________________________________________________________ This is an author produced version of a paper published in: The Journal of Antibiotics Cronfa URL for this paper: http://cronfa.swan.ac.uk/Record/cronfa41085 _____________________________________________________________ Paper: Zhang, B., Tang, S., Chen, X., Zhang, G., Zhang, W., Chen, T., Liu, G., Li, S., Dos Santos, L., et. al. (2018). Streptomyces qaidamensis sp. nov., isolated from sand in the Qaidam Basin, China. The Journal of Antibiotics http://dx.doi.org/10.1038/s41429-018-0080-9 _____________________________________________________________ This item is brought to you by Swansea University. Any person downloading material is agreeing to abide by the terms of the repository licence. Copies of full text items may be used or reproduced in any format or medium, without prior permission for personal research or study, educational or non-commercial purposes only. The copyright for any work remains with the original author unless otherwise specified. The full-text must not be sold in any format or medium without the formal permission of the copyright holder. Permission for multiple reproductions should be obtained from the original author. Authors are personally responsible for adhering to copyright and publisher restrictions when uploading content to the repository. http://www.swansea.ac.uk/library/researchsupport/ris-support/ Streptomyces qaidamensis sp. nov., isolated from sand in the Qaidam Basin, China Binglin Zhang1,2,3, Shukun Tang4, Ximing Chen1,3, Gaoseng Zhang1,3, Wei Zhang1,3, Tuo Chen2,3, Guangxiu Liu1,3, Shiweng Li3,5, Luciana Terra Dos Santos6, Helena Carla Castro6, Paul Facey7, Matthew Hitchings7 and Paul Dyson7 1 Key Laboratory of Desert and Desertification, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China. -
Halocynthia Roretzi
Sekigami et al. Zoological Letters (2017) 3:17 DOI 10.1186/s40851-017-0078-3 RESEARCH ARTICLE Open Access Hox gene cluster of the ascidian, Halocynthia roretzi, reveals multiple ancient steps of cluster disintegration during ascidian evolution Yuka Sekigami1, Takuya Kobayashi1, Ai Omi1, Koki Nishitsuji2, Tetsuro Ikuta1, Asao Fujiyama3, Noriyuki Satoh2 and Hidetoshi Saiga1* Abstract Background: Hox gene clusters with at least 13 paralog group (PG) members are common in vertebrate genomes and in that of amphioxus. Ascidians, which belong to the subphylum Tunicata (Urochordata), are phylogenetically positioned between vertebrates and amphioxus, and traditionally divided into two groups: the Pleurogona and the Enterogona. An enterogonan ascidian, Ciona intestinalis (Ci), possesses nine Hox genes localized on two chromosomes; thus, the Hox gene cluster is disintegrated. We investigated the Hox gene cluster of a pleurogonan ascidian, Halocynthia roretzi (Hr) to investigate whether Hox gene cluster disintegration is common among ascidians, and if so, how such disintegration occurred during ascidian or tunicate evolution. Results: Our phylogenetic analysis reveals that the Hr Hox gene complement comprises nine members, including one with a relatively divergent Hox homeodomain sequence. Eight of nine Hr Hox genes were orthologous to Ci-Hox1, 2, 3, 4, 5, 10, 12 and 13. Following the phylogenetic classification into 13 PGs, we designated Hr Hox genes as Hox1, 2, 3, 4, 5, 10, 11/12/13.a, 11/12/13.b and HoxX. To address the chromosomal arrangement of the nine Hox genes, we performed two-color chromosomal fluorescent in situ hybridization, which revealed that the nine Hox genes are localized on a single chromosome in Hr, distinct from their arrangement in Ci. -
1471-2148-9-187.Pdf
BMC Evolutionary Biology BioMed Central Research article Open Access An updated 18S rRNA phylogeny of tunicates based on mixture and secondary structure models Georgia Tsagkogeorga1,2, Xavier Turon3, Russell R Hopcroft4, Marie- Ka Tilak1,2, Tamar Feldstein5, Noa Shenkar5,6, Yossi Loya5, Dorothée Huchon5, Emmanuel JP Douzery1,2 and Frédéric Delsuc*1,2 Address: 1Université Montpellier 2, Institut des Sciences de l'Evolution (UMR 5554), CC064, Place Eugène Bataillon, 34095 Montpellier Cedex 05, France, 2CNRS, Institut des Sciences de l'Evolution (UMR 5554), CC064, Place Eugène Bataillon, 34095 Montpellier Cedex 05, France, 3Centre d'Estudis Avançats de Blanes (CEAB, CSIC), Accés Cala S. Francesc 14, 17300 Blanes (Girona), Spain, 4Institute of Marine Science, University of Alaska Fairbanks, Fairbanks, Alaska, USA, 5Department of Zoology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 69978, Israel and 6Department of Biology, University of Washington, Seattle WA 98195, USA Email: Georgia Tsagkogeorga - [email protected]; Xavier Turon - [email protected]; Russell R Hopcroft - [email protected]; Marie-Ka Tilak - [email protected]; Tamar Feldstein - [email protected]; Noa Shenkar - [email protected]; Yossi Loya - [email protected]; Dorothée Huchon - [email protected]; Emmanuel JP Douzery - [email protected]; Frédéric Delsuc* - [email protected] * Corresponding author Published: 5 August 2009 Received: 16 October 2008 Accepted: 5 August 2009 BMC Evolutionary Biology 2009, 9:187 doi:10.1186/1471-2148-9-187 This article is available from: http://www.biomedcentral.com/1471-2148/9/187 © 2009 Tsagkogeorga et al; licensee BioMed Central Ltd. -
Field and Laboratory Studies on Four Species of Sea Squirts and Their
Global Journal of Science Frontier Research: B Chemistry Volume 16 Issue 2 Version 1.0 Year 2016 Type : Double Blind Peer Reviewed International Research Journal Publisher: Global Journals Inc. (USA) Online ISSN: 2249-4626 & Print ISSN: 0975-5896 Field and Laboratory Studies on Four Species of Sea Squirts and their Larvae By Gaber Ahmed Saad & Abdullah Bedeer Hussein Dammam University, Saudi Arabia Abstract- The aim of this study was to characterize adult distribution with respect to light and analyze ovary contents in the four seasons of the year. The swimming behavior of Ciona intestinalis, Molgula manhattensis, Ascidella aspersa and Phallusia mammilata larvae against certain abiotic factors were commented. For the field data on adult distributions, one-way analysis of variance (ANOVA) was applied to test for differences in adult orientation, with surface orientation as a fixed factor. Two adult species (Ciona intestinalis and Molgula manhattensis) showed no orientation with respect to light while in the other two species (Ascidella aspersa and Phallusia mammilata) light exerted a significant effects on the orientation and density of individuals. To evaluate among the different species the level of gregariousness found in the field, the number of individuals per clump for each species has been compared using one-way ANOVA, with species as a fixed factor. Artificial heterologous inseminations were carried out. Keywords: field data - gregariousness - heterologous inseminations -adult orientation - larval settlement – phototaxis - geotaxis. GJSFR-B Classification : FOR Code: 069999 FieldandLaboratoryStudiesonFourSpeciesofSeaSquirtsandtheirLarvae Strictly as per the compliance and regulations of : © 2016. Gaber Ahmed Saad & Abdullah Bedeer Hussein. This is a research/review paper, distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License http://creativecommons.org/licenses/by-nc/3.0/), permitting all non commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. -
Missouri's Toads and Frogs Booklet
TOADSMissouri’s andFROGS by Jeffrey T. Briggler and Tom R. Johnson, Herpetologists www.MissouriConservation.org © 1982, 2008 Missouri Conservation Commission Equal opportunity to participate in and benefit from programs of the Missouri Department of Conservation is available to all individuals without regard to their race, color, national origin, sex, age or disability. Questions should be directed to the Department of Conservation, P.O. Box 180, Jefferson City, MO 65102, (573) 751-4115 (voice) or 800-735-2966 (TTY), or to the U.S. Fish and Wildlife Service Division of Federal Assistance, 4401 N. Fairfax Drive, Mail Stop: MBSP-4020, Arlington, VA 22203. Cover photo: Eastern gray treefrog by Tom R. Johnson issouri toads and frogs are colorful, harmless, vocal and valuable. Our forests, prairies, rivers, swamps and marshes are Mhome to a multitude of toads and frogs, but few people know how many varieties we have, how to tell them apart, or much about their natural history. Studying these animals and sharing their stories with fellow Missourians is one of the most pleasurable and rewarding aspects of our work. Toads and frogs are amphibians—a class Like most of vertebrate animals that also includes amphibians, salamanders and the tropical caecilians, which are long, slender, wormlike and legless. frogs and Missouri has 26 species and subspecies (or toads have geographic races) of toads and frogs. Toads and frogs differ from salamanders by having an aquatic relatively short bodies and lacking tails at adulthood. Being an amphibian means that tadpole stage they live two lives: an aquatic larval or tadpole and a semi- stage and a semi-aquatic or terrestrial adult stage.