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Effects of Food Type, Feeding Frequency, and Temperature on Juvenile Survival and Growth of Marisa Cornuarietis (Mollusca: Gastropoda)
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Valery Forbes Publications Papers in the Biological Sciences 2006 Effects of food type, feeding frequency, and temperature on juvenile survival and growth of Marisa cornuarietis (Mollusca: Gastropoda) Henriette Selck Roskilde University, [email protected] John Aufderheide ABC Laboratories, Inc., Columbia, Missouri Nadine Pounds Brixham Environmental Laboratory, AstraZeneca, Devon, UK Charles Staples Assessment Technologies Inc., Fredericksburg, Virginia Norbert Caspers Bayer AG, Institute for Environmental Analysis and Evaluation, Leverkusen, Germany See next page for additional authors Follow this and additional works at: https://digitalcommons.unl.edu/biosciforbes Part of the Pharmacology, Toxicology and Environmental Health Commons Selck, Henriette; Aufderheide, John; Pounds, Nadine; Staples, Charles; Caspers, Norbert; and Forbes, Valery E., "Effects of food type, feeding frequency, and temperature on juvenile survival and growth of Marisa cornuarietis (Mollusca: Gastropoda)" (2006). Valery Forbes Publications. 32. https://digitalcommons.unl.edu/biosciforbes/32 This Article is brought to you for free and open access by the Papers in the Biological Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Valery Forbes Publications by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Authors Henriette Selck, John Aufderheide, Nadine Pounds, Charles Staples, Norbert Caspers, and Valery -
Freshwater Snail Guide
A Beginner’s Guide to Freshwater Snails of Central Scotland Freshwater snails are a diverse and fascinating group of molluscs found in ponds, lochs, canals, rivers and watery ditches all across the globe. This guide is a simple introduction to some of the most commonly encountered and easily identifiable freshwater snail species in Central Scotland. How do I look for freshwater snails? 1) Choose your spot: anywhere with water – your garden pond, a nearby river, canal or loch – is likely to have snails. 2) Grab a pond net (buy online or make your own by attaching a sieve to the end of an old broom or mop), a white tray or tub and a hand-lens or magnifier. 3) Fill the tray with water from your chosen habitat. Sweep the net around in the water, making sure to get among any vegetation (don’t go too near the bottom or you’ll get a net full of mud), empty your net into the water-filled tray and identify what you have found! Snail shell features Spire Whorls Some snail species have a hard plate called an ‘operculum’ Height which they Mouth (Aperture) use to seal the mouth of the shell when they are inside Height Pointed shell Flat shell Width Width Pond Snails (Lymnaeidae) Variable in size. Mouth always on right-hand side, shells usually long and pointed. Great Pond Snail Common Pond Snail Lymnaea stagnalis Radix balthica Largest pond snail. Common in ponds Fairly rounded and ’fat’. Common in weedy lakes, canals and sometimes slow river still waters. pools. -
Pomacea Canaliculata) Behaviors in Different Water Temperature Gradients
water Article Comparison of Invasive Apple Snail (Pomacea canaliculata) Behaviors in Different Water Temperature Gradients Mi-Jung Bae 1, Eui-Jin Kim 1 and Young-Seuk Park 2,* 1 Nakdonggang National Institute of Biological Resources, Sangju 37242, Korea; [email protected] (M.-J.B.); [email protected] (E.-J.K.) 2 Department of Biology, Kyung Hee University, Dongdaemun, Seoul 02447, Korea * Correspondence: [email protected]; Tel.: +82-2-961-0946 Abstract: Pomacea canaliculata (known as invasive apple snail) is a freshwater snail native to South America that was introduced into many countries (including Asia and North America) as a food source or for organic farming systems. However, it has invaded freshwater ecosystems and become a serious agricultural pest in paddy fields. Water temperature is an important factor determining behavior and successful establishment in new areas. We examined the behavioral responses of P. canaliculata with water temperature changes from 25 ◦C to 30 ◦C, 20 ◦C, and 15 ◦C by quantifying changes in nine behaviors. At the acclimated temperature (25 ◦C), the mobility of P. canaliculata was low during the day, but high at night. Clinging behavior increased as the water temperature decreased from 25 ◦C to 20 ◦C or 15 ◦C. Conversely, ventilation and food consumption increased when the water temperature increased from 25 ◦C to 30 ◦C. A self-organizing map (an unsupervised artificial neural network) was used to classify the behavioral patterns into seven clusters at different water temperatures. These results suggest that the activity levels or certain behaviors of P. canaliculata vary with the water temperature conditions. -
Gastropoda: Physidae) in Singapore
BioInvasions Records (2015) Volume 4, Issue 3: 189–194 Open Access doi: http://dx.doi.org/10.3391/bir.2015.4.3.06 © 2015 The Author(s). Journal compilation © 2015 REABIC Research Article Clarifying the identity of the long-established, globally-invasive Physa acuta Draparnaud, 1805 (Gastropoda: Physidae) in Singapore Ting Hui Ng1,2*, Siong Kiat Tan3 and Darren C.J. Yeo1,2 1Department of Biological Sciences, National University of Singapore 14 Science Drive 4, Singapore 117543, Republic of Singapore 2NUS Environmental Research Institute, National University of Singapore, 5A Engineering Drive 1, #02-01, Singapore 117411, Republic of Singapore 3Lee Kong Chian Natural History Museum, National University of Singapore, 2 Conservatory Drive, Singapore 117377, Republic of Singapore E-mail: [email protected] (THN), [email protected] (SKT), [email protected] (DCJY) *Corresponding author Received: 24 December 2014 / Accepted: 6 May 2015 / Published online: 2 June 2015 Handling editor: Vadim Panov Abstract The freshwater snail identified as Physastra sumatrana has been recorded in Singapore since the late 1980’s. It is distributed throughout the island and commonly associated with ornamental aquatic plants. Although the species has previously been considered by some to be native to Singapore, its origin is currently categorised as unknown. Morphological comparisons of freshly collected specimens and material in museum collections with type material, together with DNA barcoding, show that both Physastra sumatrana, and a recent gastropod record of Stenophysa spathidophallus, in Singapore are actually the same species—the globally-invasive Physa acuta. An unidentified physid snail was also collected from the Singapore aquarium trade. -
(Strombus Gigas) in Colombia
NDF WORKSHOP CASE STUDIES WG 9 – Aquatic Invertebrates CASE STUDY 3 Strombus gigas Country – COLOMBIA Original language – English NON-DETRIMENTAL FINDINGS FOR THE QUEEN CONCH (STROMBUS GIGAS) IN COLOMBIA AUTHORS: Martha Prada1 Erick Castro2 Elizabeth Taylor1 Vladimir Puentes3 Richard Appeldoorn4 Nancy Daves5 1 CORALINA 2 Secretaria de Agricultura y Pesca 3 Ministerio de Medio Ambiente, Vivienda y Desarrollo Territorial 4 Universidad Puerto Rico – Caribbean Coral Reef Institute 5 NOAA Fisheries I. BACKGROUND INFORMATION ON THE TAXA The queen conch (Strombus gigas) has been a highly prized species since pre-Columbian times, dating the period of the Arawak and Carib Indians. Early human civilizations utilized the shell as a horn for reli- gious ceremonies, for trade and ornamentation such as bracelets, hair- pins, and necklaces. Archeologists have also found remnants of conch shell pieces that were used as tools, possibly to hollow out large trees once used as canoes (Brownell and Stevely 1981). The earliest record of commercial harvest and inter-island trade extend from the mid 18th century, when dried conch meat was shipped from the Turks and Caicos Islands to the neighboring island of Hispaniola (Ninnes 1984). In Colombia, queen conch constitutes one of the most important Caribbean fisheries, it is second in value, after the spiny lobster. The oceanic archipelago of San Andrés, Providence and Santa Catalina pro- duces more than 95% country’s total production of this species. This fishery began in the 1970´s when the continental-shelf archipelagos of San Bernardo and Rosario, following full exploitation were quickly depleted due to a lack of effective management (Mora 1994). -
Mollusca, Archaeogastropoda) from the Northeastern Pacific
Zoologica Scripta, Vol. 25, No. 1, pp. 35-49, 1996 Pergamon Elsevier Science Ltd © 1996 The Norwegian Academy of Science and Letters Printed in Great Britain. All rights reserved 0300-3256(95)00015-1 0300-3256/96 $ 15.00 + 0.00 Anatomy and systematics of bathyphytophilid limpets (Mollusca, Archaeogastropoda) from the northeastern Pacific GERHARD HASZPRUNAR and JAMES H. McLEAN Accepted 28 September 1995 Haszprunar, G. & McLean, J. H. 1995. Anatomy and systematics of bathyphytophilid limpets (Mollusca, Archaeogastropoda) from the northeastern Pacific.—Zool. Scr. 25: 35^9. Bathyphytophilus diegensis sp. n. is described on basis of shell and radula characters. The radula of another species of Bathyphytophilus is illustrated, but the species is not described since the shell is unknown. Both species feed on detached blades of the surfgrass Phyllospadix carried by turbidity currents into continental slope depths in the San Diego Trough. The anatomy of B. diegensis was investigated by means of semithin serial sectioning and graphic reconstruction. The shell is limpet like; the protoconch resembles that of pseudococculinids and other lepetelloids. The radula is a distinctive, highly modified rhipidoglossate type with close similarities to the lepetellid radula. The anatomy falls well into the lepetelloid bauplan and is in general similar to that of Pseudococculini- dae and Pyropeltidae. Apomorphic features are the presence of gill-leaflets at both sides of the pallial roof (shared with certain pseudococculinids), the lack of jaws, and in particular many enigmatic pouches (bacterial chambers?) which open into the posterior oesophagus. Autapomor- phic characters of shell, radula and anatomy confirm the placement of Bathyphytophilus (with Aenigmabonus) in a distinct family, Bathyphytophilidae Moskalev, 1978. -
Abstract Volume
ABSTRACT VOLUME August 11-16, 2019 1 2 Table of Contents Pages Acknowledgements……………………………………………………………………………………………...1 Abstracts Symposia and Contributed talks……………………….……………………………………………3-225 Poster Presentations…………………………………………………………………………………226-291 3 Venom Evolution of West African Cone Snails (Gastropoda: Conidae) Samuel Abalde*1, Manuel J. Tenorio2, Carlos M. L. Afonso3, and Rafael Zardoya1 1Museo Nacional de Ciencias Naturales (MNCN-CSIC), Departamento de Biodiversidad y Biologia Evolutiva 2Universidad de Cadiz, Departamento CMIM y Química Inorgánica – Instituto de Biomoléculas (INBIO) 3Universidade do Algarve, Centre of Marine Sciences (CCMAR) Cone snails form one of the most diverse families of marine animals, including more than 900 species classified into almost ninety different (sub)genera. Conids are well known for being active predators on worms, fishes, and even other snails. Cones are venomous gastropods, meaning that they use a sophisticated cocktail of hundreds of toxins, named conotoxins, to subdue their prey. Although this venom has been studied for decades, most of the effort has been focused on Indo-Pacific species. Thus far, Atlantic species have received little attention despite recent radiations have led to a hotspot of diversity in West Africa, with high levels of endemic species. In fact, the Atlantic Chelyconus ermineus is thought to represent an adaptation to piscivory independent from the Indo-Pacific species and is, therefore, key to understanding the basis of this diet specialization. We studied the transcriptomes of the venom gland of three individuals of C. ermineus. The venom repertoire of this species included more than 300 conotoxin precursors, which could be ascribed to 33 known and 22 new (unassigned) protein superfamilies, respectively. Most abundant superfamilies were T, W, O1, M, O2, and Z, accounting for 57% of all detected diversity. -
CINCINNATIAN GASTROPOD PRIMER by Ron Fine HOW DO SCIENTISTS CLASSIFY GASTROPODS?
CINCINNATIAN GASTROPOD PRIMER By Ron Fine HOW DO SCIENTISTS CLASSIFY GASTROPODS? KINGDOM: Animalia (Animals) Mammals Birds Fish Amphibians Molluscs Insects PHYLUM: Mollusca (Molluscs) Cephalopods Gastropods Bivalves Monoplacophorans Scaphopods Aplacophorans Polyplacophorans CLASS: Gastropoda (Gastropods or Snails) Gastropods 2 HOW MANY KINDS OF GASTROPODS ARE THERE? There are 611 Families of gastropods, but 202 are now extinct Whelk Slug Limpet Land Snail Conch Periwinkle Cowrie Sea Butterfly Nudibranch Oyster Borer 3 THERE ARE 60,000 TO 80,000 SPECIES! IN ENDLESS SHAPES AND PATTERNS! 4 HABITAT-WHERE DO GASTROPODS LIVE? Gardens Deserts Ocean Depths Mountains Ditches Rivers Lakes Estuaries Mud Flats Tropical Rain Forests Rocky Intertidal Woodlands Subtidal Zones Hydrothermal Vents Sub-Arctic/Antarctic Zones 5 HABITAT-WHAT WAS IT LIKE IN THE ORDOVICIAN? Gastropods in the Ordovician of Cincinnati lived in a tropical ocean, much like the Caribbean of today 6 DIET-WHAT DO GASTROPODS EAT? Herbivores Detritus Parasites Plant Eaters Mud Eaters Living on other animals Scavengers Ciliary Carnivores Eat dead animals Filter feeding in the water Meat Eaters 7 ANATOMY-HOW DO YOU IDENTIFY A GASTROPOD? Gastropod is Greek, from “gaster” meaning ‘stomach’ and “poda” meaning ‘foot’ They are characterized by a head with antennae, a large foot, coiled shell, a radula and operculum Torsion: all of a gastropod’s anatomy is twisted, not just the shell They are the largest group of molluscs, only insects are more diverse Most are hermaphrodites 8 GASTROPOD ANATOMY-FOOT Gastropods have a large “foot”, used for locomotion. Undulating bands of muscles propel the gastropod forward, even on vertical surfaces. SLIME! Gastropods excrete slime to help their foot glide over almost any surface. -
Structure and Function of the Digestive System in Molluscs
Cell and Tissue Research (2019) 377:475–503 https://doi.org/10.1007/s00441-019-03085-9 REVIEW Structure and function of the digestive system in molluscs Alexandre Lobo-da-Cunha1,2 Received: 21 February 2019 /Accepted: 26 July 2019 /Published online: 2 September 2019 # Springer-Verlag GmbH Germany, part of Springer Nature 2019 Abstract The phylum Mollusca is one of the largest and more diversified among metazoan phyla, comprising many thousand species living in ocean, freshwater and terrestrial ecosystems. Mollusc-feeding biology is highly diverse, including omnivorous grazers, herbivores, carnivorous scavengers and predators, and even some parasitic species. Consequently, their digestive system presents many adaptive variations. The digestive tract starting in the mouth consists of the buccal cavity, oesophagus, stomach and intestine ending in the anus. Several types of glands are associated, namely, oral and salivary glands, oesophageal glands, digestive gland and, in some cases, anal glands. The digestive gland is the largest and more important for digestion and nutrient absorption. The digestive system of each of the eight extant molluscan classes is reviewed, highlighting the most recent data available on histological, ultrastructural and functional aspects of tissues and cells involved in nutrient absorption, intracellular and extracellular digestion, with emphasis on glandular tissues. Keywords Digestive tract . Digestive gland . Salivary glands . Mollusca . Ultrastructure Introduction and visceral mass. The visceral mass is dorsally covered by the mantle tissues that frequently extend outwards to create a The phylum Mollusca is considered the second largest among flap around the body forming a space in between known as metazoans, surpassed only by the arthropods in a number of pallial or mantle cavity. -
Mollusca: Gastropoda) from Islands Off the Kimberley Coast, Western Australia Frank Köhler1, Vince Kessner2 and Corey Whisson3
RECORDS OF THE WESTERN AUSTRALIAN MUSEUM 27 021–039 (2012) New records of non-marine, non-camaenid gastropods (Mollusca: Gastropoda) from islands off the Kimberley coast, Western Australia Frank Köhler1, Vince Kessner2 and Corey Whisson3 1 Department of Environment and Conservation of Western Australia, Science Division, PO Box 51, Wanneroo, Western Australia 6946; and Australian Museum, 6 College Street, Sydney, New South Wales 2010, Australia. Email: [email protected] 2 162 Haynes Road, Adelaide River, Northern Terrritory 0846, Australia. Email: [email protected] 3 Department of Aquatic Zoology, Western Australian Museum, 49 Kew Street, Welshpool, Western Australia 6106, Australia. Email: [email protected] ABSTRACT – The coast of the Western Australian Kimberley boasts an archipelago that comprises several hundred large islands and thousands much smaller. While the non–marine gastropod fauna of the Kimberley mainland has been surveyed to some extent, the fauna of these islands had never been comprehensively surveyed and only anecdotal and unsystematic data on species occurrences have been available. During the Western Australian Department of Environment and Conservation’s Kimberley Island Survey, 2008–2010, 22 of the largest islands were surveyed. Altogether, 17 species of terrestrial non–camaenid snails were found on these islands. This corresponds to about 75% of all terrestrial, non–camaenid gastropods known from the entire Kimberley region. In addition, four species of pulmonate freshwater snails were found to occur on one or more of four of these islands. Individual islands harbour up to 15, with an average of eight, species each. Species diversity was found to be higher in the wetter parts of the region. -
A Transcriptome Database for Eight Species of Apple Snails (Gastropoda: Ampullariidae) Jack C
Ip et al. BMC Genomics (2018) 19:179 https://doi.org/10.1186/s12864-018-4553-9 DATABASE Open Access AmpuBase: a transcriptome database for eight species of apple snails (Gastropoda: Ampullariidae) Jack C. H. Ip1,2, Huawei Mu1, Qian Chen3, Jin Sun4, Santiago Ituarte5, Horacio Heras5,6, Bert Van Bocxlaer7,8, Monthon Ganmanee9, Xin Huang3* and Jian-Wen Qiu1,2* Abstract Background: Gastropoda, with approximately 80,000 living species, is the largest class of Mollusca. Among gastropods, apple snails (family Ampullariidae) are globally distributed in tropical and subtropical freshwater ecosystems and many species are ecologically and economically important. Ampullariids exhibit various morphological and physiological adaptations to their respective habitats, which make them ideal candidates for studying adaptation, population divergence, speciation, and larger-scale patterns of diversity, including the biogeography of native and invasive populations. The limited availability of genomic data, however, hinders in-depth ecological and evolutionary studies of these non-model organisms. Results: Using Illumina Hiseq platforms, we sequenced 1220 million reads for seven species of apple snails. Together with the previously published RNA-Seq data of two apple snails, we conducted de novo transcriptome assembly of eight species that belong to five genera of Ampullariidae, two of which represent Old World lineages and the other three New World lineages. There were 20,730 to 35,828 unigenes with predicted open reading frames for the eight species, with N50 (shortest sequence length at 50% of the unigenes) ranging from 1320 to 1803 bp. 69.7% to 80.2% of these unigenes were functionally annotated by searching against NCBI’s non-redundant, Gene Ontology database and the Kyoto Encyclopaedia of Genes and Genomes. -
The Golden Apple Snail: Pomacea Species Including Pomacea Canaliculata (Lamarck, 1822) (Gastropoda: Ampullariidae)
The Golden Apple Snail: Pomacea species including Pomacea canaliculata (Lamarck, 1822) (Gastropoda: Ampullariidae) DIAGNOSTIC STANDARD Prepared by Robert H. Cowie Center for Conservation Research and Training, University of Hawaii, 3050 Maile Way, Gilmore 408, Honolulu, Hawaii 96822, USA Phone ++1 808 956 4909, fax ++1 808.956 2647, e-mail [email protected] 1. PREFATORY COMMENTS The term ‘apple snail’ refers to species of the freshwater snail family Ampullariidae primarily in the genera Pila, which is native to Asia and Africa, and Pomacea, which is native to the New World. They are so called because the shells of many species in these two genera are often large and round and sometimes greenish in colour. The term ‘golden apple snail’ is applied primarily in south-east Asia to species of Pomacea that have been introduced from South America; ‘golden’ either because of the colour of their shells, which is sometimes a bright orange-yellow, or because they were seen as an opportunity for major financial success when they were first introduced. ‘Golden apple snail’ does not refer to a single species. The most widely introduced species of Pomacea in south-east Asia appears to be Pomacea canaliculata (Lamarck, 1822) but at least one other species has also been introduced and is generally confused with P. canaliculata. At this time, even mollusc experts are not able to distinguish the species readily or to provide reliable scientific names for them. This confusion results from the inadequate state of the systematics of the species in their native South America, caused by the great intra-specific morphological variation that exists throughout the wide distributions of the species.