Erythrinus Erythrinus (No Common Name) Ecological Risk Screening Summary
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O2 Secretion in the Eye and Swimbladder of Fishes
1641 The Journal of Experimental Biology 209, 1641-1652 Published by The Company of Biologists 2007 doi:10.1242/jeb.003319 Historical reconstructions of evolving physiological complexity: O2 secretion in the eye and swimbladder of fishes Michael Berenbrink School of Biological Sciences, The University of Liverpool, Biosciences Building, Crown Street, Liverpool, L69 7ZB, UK e-mail: [email protected] Accepted 12 March 2007 Summary The ability of some fishes to inflate their compressible value of haemoglobin. These changes predisposed teleost swimbladder with almost pure oxygen to maintain neutral fishes for the later evolution of swimbladder oxygen buoyancy, even against the high hydrostatic pressure secretion, which occurred at least four times independently several thousand metres below the water surface, has and can be associated with increased auditory sensitivity fascinated physiologists for more than 200·years. This and invasion of the deep sea in some groups. It is proposed review shows how evolutionary reconstruction of the that the increasing availability of molecular phylogenetic components of such a complex physiological system on a trees for evolutionary reconstructions may be as important phylogenetic tree can generate new and important insights for understanding physiological diversity in the post- into the origin of complex phenotypes that are difficult to genomic era as the increase of genomic sequence obtain with a purely mechanistic approach alone. Thus, it information in single model species. is shown that oxygen secretion first evolved in the eyes of fishes, presumably for improved oxygen supply to an Glossary available online at avascular, metabolically active retina. Evolution of this http://jeb.biologists.org/cgi/content/full/210/9/1641/DC1 system was facilitated by prior changes in the pH dependence of oxygen-binding characteristics of Key words: oxygen secretion, Root effect, rete mirabile, choroid, haemoglobin (the Root effect) and in the specific buffer swimbladder, phylogenetic reconstruction. -
Notes on the Swim-Bladder Physiology of Cod (Gadus Morhua) Investigated from the Underwater Laboratory "Helgoland"
Helgol~inder wiss. Meeresunters. 29, 460-463 (1977) Notes on the swim-bladder physiology of cod (Gadus morhua) investigated from the underwater laboratory "Helgoland" G. SUNDNES, B. GULLIKSEN ~X~ J. MORK Biological stasjon; Trondheim, Norway ABSTRACT: In situ sampling of gas from cod swim-bladders took place during a fortnight's saturation mission with the underwater laboratory "Helgoland" in May-June I975. These samples were compared to those done by the conventional method of transporting the fish to the surface for sampling. Based upon these in-situ measurements, the mean O2-concentration was 55.7 °/0 in buoyant cod at 15 m depth. Repeated sampling of the same fish showed a change in gas composition. Compared to the conventional method of transporting fish for sampling to the surface, in-situ sampling gave results with less variation, and indicated that surface-sampling does not give the correct gas composition of buoyant fish at depth of catch. INTRODUCTION Physiological investigations of fish swim-bladder have usually been performed near the surface, i.e. at about one atmosphere pressure. It means that fish were usually brought to the surface from their natural habitat of high water pressure to reduced pressure before experiments were performed and samples taken. Even in experiments with fish in pressure chambers, the gas samples of the swim-bladder were taken at one atmosphere pressure. Gas sampIes from fish at the depth of buoyancy have rarely been reported. The development of the underwater laboratory has given marine biologists a better opportunity to work under hydrostatic pressure whereby fish are kept under "natural" experimental conditions. -
Analysis of the Diet Between an Invasive and Native Fishes in the Peruvian Amazon. Anthony Mazeroll [email protected] Introduct
Analysis of the diet between an invasive and native fishes in the Peruvian Amazon. Anthony Mazeroll [email protected] Introduction Non-native species are the second greatest threat to global species biodiversity after land development (Vitousek, D'Antonio, Loope, Rejmanek, & Westbrooks, 1997). Due to the magnitude of this threat, it is vital that the impacts of exotic species are understood. Fish biodiversity is especially threatened by the ecological changes caused by non-native species (Gozlan, Britton, Cowx, & Copp, 2010). Having higher species diversity allows more ecological processes to take place, protecting the resources of that system, and making it more resilient to change (Folke, 2006). Adding outside inputs, such as additional non-native species, into an ecosystem can have beneficial or compromising effects depending on the amount and type. Invasive species have been shown to reduce native species richness and diversity of native organisms. Some have argued that the transportation of species from one ecosystem to another is actually beneficial for diversity, and non-native species are not really an environmental “problem”. Introductions of non-native species increase diversity at a local level because in the short term there will be a lag time where both non-native and natives can coexist (Lodge, Stein, Brown, Covich, Bronmark, Garvey and Klosiewski, 1998). Species entering a new ecosystem have to pass through a gauntlet of barriers before they can become established. The usual progression of invasion is: transportation to the new ecosystem, initial establishment, spread to a larger region, and then naturalization into the new community (Marchetti, Light, Moyle, and Viers, 2004). -
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S. Fish and Wildlife Service Region 4—An Update April 2013 Prepared by: Pam L. Fuller, Amy J. Benson, and Matthew J. Cannister U.S. Geological Survey Southeast Ecological Science Center Gainesville, Florida Prepared for: U.S. Fish and Wildlife Service Southeast Region Atlanta, Georgia Cover Photos: Silver Carp, Hypophthalmichthys molitrix – Auburn University Giant Applesnail, Pomacea maculata – David Knott Straightedge Crayfish, Procambarus hayi – U.S. Forest Service i Table of Contents Table of Contents ...................................................................................................................................... ii List of Figures ............................................................................................................................................ v List of Tables ............................................................................................................................................ vi INTRODUCTION ............................................................................................................................................. 1 Overview of Region 4 Introductions Since 2000 ....................................................................................... 1 Format of Species Accounts ...................................................................................................................... 2 Explanation of Maps ................................................................................................................................ -
Erythrinidae
FAMILY Erythrinidae Valenciennes, in Cuvier & Valenciennes, 1947 - trahiras [=Erythricthini, Erythroides, Hopliidi] Notes: Name in prevailing recent practice, Article 35.5 Erythricthini [Erythrichthini] Bonaparte 1835:[16] [ref. 32242] (subfamily) Erythrichthys [genus inferred from the stem, Article 11.7.1.1; corrected to Erythrichthini by Bonaparte 1837:[7] [ref. 32243]; senior objective synonym of Erythrinidae Valenciennes, 1847, but not used as valid after 1899] Érythroïdes Valenciennes, in Cuvier & Valenciennes, 1847:480 [ref. 4883] (family) Erythrinus [latinized to Erythrinidae by Richardson 1856:250 [ref. 3747], confirmed by Gill 1858:410 [ref. 1750] and by Cope 1872:257 [ref. 921]; considered valid with this authorship by Richardson 1856:250 [ref. 3747], by Gill 1893b:131 [ref. 26255] and by Sheiko 2013:44 [ref. 32944] Article 11.7.2; junior objective synonym of Erythrichthini Bonaparte, 1835, but in prevailing recent practice; Erythrinidae also used as valid by: McAllister 1968 [ref. 26854], Lindberg 1971 [ref. 27211], Géry 1972b [ref. 1594], Nelson 1976 [ref.32838], Shiino 1976, Géry 1977 [ref. 1597], Nelson 1984 [ref. 13596], Sterba 1990, Nelson 1994 [ref. 26204], Springer & Raasch 1995:104 [ref. 25656], Eschmeyer 1998 [ref. 23416], Malabarba et al. 1998 [ref. 23777], Reis et al. 2003 [ref. 27061], Nelson 2006 [ref. 32486], Buckup, Menezes & Ghazzi 2007, Oyakawa & Mattox 2009 [ref. 30225], Jacobina, Paiva & Dergam 2011 [ref. 31391]] Hopliidi Fowler, 1958b:9 [ref. 1470] (tribe) Hoplias GENUS Erythrinus Scopoli, 1777 - trahiras [=Erythrinus Scopoli [J. A.] (ex Gronow), 1777:449, Erythrichthys Bonaparte [C. L.], 1831:182, Erythrinus Gronow [L. T.], 1763:114, Hetererythrinus (subgenus of Erythrinus) Günther [A.], 1864:283, 284] Notes: [ref. 3990]. -
Turnover of Sex Chromosomes and Speciation in Fishes
Environ Biol Fish (2012) 94:549–558 DOI 10.1007/s10641-011-9853-8 Turnover of sex chromosomes and speciation in fishes Jun Kitano & Catherine L. Peichel Received: 1 December 2010 /Accepted: 8 May 2011 /Published online: 4 June 2011 # The Author(s) 2011. This article is published with open access at Springerlink.com Abstract Closely related species of fishes often have threespine stickleback population has a simple XY different sex chromosome systems. Such rapid turnover sex chromosome system. Furthermore, we demon- of sex chromosomes can occur by several mechanisms, strated that the neo-X chromosome (X2)playsan including fusions between an existing sex chromosome important role in phenotypic divergence and repro- and an autosome. These fusions can result in a multiple ductive isolation between these sympatric stickle- sex chromosome system, where a species has both an back species pairs. Here, we review multiple sex ancestral and a neo-sex chromosome. Although this chromosome systems in fishes, as well as recent type of multiple sex chromosome system has been advances in our understanding of the evolutionary found in many fishes, little is known about the role of sex chromosome turnover in stickleback mechanisms that select for the formation of neo-sex speciation. chromosomes, or the role of neo-sex chromosomes in phenotypic evolution and speciation. The identification Keywords Multiple sex chromosomes . Neo-sex of closely related, sympatric species pairs in which one chromosome . X1X2Y. Stickleback . Sexual conflict . species has a multiple sex chromosome system and Speciation the other has a simple sex chromosome system provides an opportunity to study sex chromosome turnover. -
Hoplias Malabaricus (Guabine) Family: Erythrinidae (Trahiras) Order: Characiformes (Characins and Allied Fish) Class: Actinopterygii (Ray-Finned Fish)
UWI The Online Guide to the Animals of Trinidad and Tobago Behaviour Hoplias malabaricus (Guabine) Family: Erythrinidae (Trahiras) Order: Characiformes (Characins and Allied Fish) Class: Actinopterygii (Ray-finned Fish) Fig. 1. Guabine, Hoplias malabaricus. [http://upload.wikimedia.org/wikipedia/commons/thumb/3/34/Hoplias_malabaricus1.jpg/800px- Hoplias_malabaricus1.jpg , downloaded 13 November 2012] TRAITS. The guabine, Hoplias malabaricus, is also known as wolf-fish or tahira in Trinidad and Tobago (Phillip & Ramnarine 2001). This freshwater fish can grow up to 40 cm in length and can weigh more than 1.5 kg (Kenny 2008). The shape is cylindrical and it has a large mouth since it is a predatory creature. The name wolf-fish was given to the guabine due to the presence of the dog-like teeth. When bitten, the jaws of this fish are locked onto the prey (Kenny 2008). The coloration of the guabine fish is usually dark brown or grey as seen in Fig.1 above with either darker vertical stripes or a single horizontal stripe on the body (Wikipedia, 2012) so that they can camouflage and hunt better. The fish can be identified and distinguished from other species by the shape of the under-jaw where a V-shape is formed when the inside jaw lines come to the front of the fish (Cousins 2011). The juvenile stages of the guabine resemble the adult forms with the exception of the size where the juveniles are more slender than the adults. According to Cousins (2011), the females have a bigger build than the males. UWI The Online Guide to the Animals of Trinidad and Tobago Behaviour ECOLOGY. -
The Secretion of Oxygen Into the Swim-Bladder of Fish III
CORE Metadata, citation and similar papers at core.ac.uk Provided by PubMed Central The Secretion of Oxygen into the Swim-Bladder of Fish III. The role of carbon dioxide JONATHAN B. WITTENBERG, MARY J. SCHWEND, and BEATRICE A. WITTENBERG From the Department of Physiology, Albert Einstein College of Medicine, Yeshiva University, New York, and the Marine Biological Laboratory, Woods Hole, Massachusetts ABSTRACT The secretion of carbon dioxide accompanying the secretion of oxygen into the swim-bladder of the bluefish is examined in order to distinguish among several theories which have been proposed to describe the operation of the rete mirabile, a vascular countercurrent exchange organ. Carbon dioxide may comprise 27 per cent of the gas secreted, corresponding to a partial pres- sure of 275 mm Hg. This is greater than the partial pressure that would be generated by acidifying arterial blood (about 55 mm Hg). The rate of secretion is very much greater than the probable rate of metabolic formation of carbon dioxide in the gas-secreting complex. It is approximately equivalent to the probable rate of glycolytic generation of lactic acid in the gas gland. It is con- cluded that carbon dioxide brought into the swim-bladder is liberated from blood by the addition of lactic acid. The rete mirabile must act to multiply the primary partial pressure of carbon dioxide produced by acidification of the blood. The function of the rete mirabile as a countercutrent multiplier has been proposed by Kuhn, W., Ramel, A., Kuhn, H. J., and Marti, E., Experientia, 1963, 19, 497. Our findings provide strong support for their theory. -
A New Myxozoan Species Henneguya Unitaeniata Sp. Nov. (Cnidaria
Parasitology Research (2019) 118:3327–3336 https://doi.org/10.1007/s00436-019-06533-1 FISH PARASITOLOGY - ORIGINAL PAPER A new myxozoan species Henneguya unitaeniata sp.nov.(Cnidaria: Myxosporea) on gills of Hoplerythrinus unitaeniatus from Mato Grosso State, Brazil Letícia Pereira Úngari1 & Diego Henrique Mirandola Dias Vieira1 & Reinaldo José da Silva1 & André Luiz Quagliatto Santos2 & Rodney Kozlowiski de Azevedo3 & Lucia Helena O’Dwyer1 Received: 15 May 2019 /Accepted: 28 October 2019 /Published online: 15November 2019 # Springer-Verlag GmbH Germany, part of Springer Nature 2019 Abstract On the basis of morphological and molecular analyses, a new myxozoan parasite is described from the gills of the fish Hoplerythrinus unitaeniatus, collected in the municipality of Nova Xavantina, Mato Grosso State, Brazil. Plasmodia of Henneguya unitaeniata sp. nov. were oval and whitish and were found surrounded by collagen fibers forming plasmodia wall between gill filaments on the gill arch. The spores were ellipsoidal with two similar polar capsules. Morphometric analysis showed a total spore mean length of 23.8 ± 1.5 μm, spore body mean length of 14.5 ± 0.7 μm, caudal appendage mean length of 10.3 ± 1.4 μm,thicknessmeanlengthof4.3±0.3μm, polar capsule mean length of 4.2 ± 0.5 μm, polar capsule mean width of 1.8 ± 0.3 μm, spore mean width of 4.8 ± 0.4 μm, and 4–5 polar filament coils. Phylogenetic analysis showed Henneguya unitaeniata sp. nov. as a basal species in a subclade formed by myxozoans that parasitize bryconid fishes. Keywords Erythrinidae . Histopathology . Myxobolidae . Phylogeny . SSU rDNA Introduction H. cinereus Gill 1858, H. -
A Rapid Biological Assessment of the Upper Palumeu River Watershed (Grensgebergte and Kasikasima) of Southeastern Suriname
Rapid Assessment Program A Rapid Biological Assessment of the Upper Palumeu River Watershed (Grensgebergte and Kasikasima) of Southeastern Suriname Editors: Leeanne E. Alonso and Trond H. Larsen 67 CONSERVATION INTERNATIONAL - SURINAME CONSERVATION INTERNATIONAL GLOBAL WILDLIFE CONSERVATION ANTON DE KOM UNIVERSITY OF SURINAME THE SURINAME FOREST SERVICE (LBB) NATURE CONSERVATION DIVISION (NB) FOUNDATION FOR FOREST MANAGEMENT AND PRODUCTION CONTROL (SBB) SURINAME CONSERVATION FOUNDATION THE HARBERS FAMILY FOUNDATION Rapid Assessment Program A Rapid Biological Assessment of the Upper Palumeu River Watershed RAP (Grensgebergte and Kasikasima) of Southeastern Suriname Bulletin of Biological Assessment 67 Editors: Leeanne E. Alonso and Trond H. Larsen CONSERVATION INTERNATIONAL - SURINAME CONSERVATION INTERNATIONAL GLOBAL WILDLIFE CONSERVATION ANTON DE KOM UNIVERSITY OF SURINAME THE SURINAME FOREST SERVICE (LBB) NATURE CONSERVATION DIVISION (NB) FOUNDATION FOR FOREST MANAGEMENT AND PRODUCTION CONTROL (SBB) SURINAME CONSERVATION FOUNDATION THE HARBERS FAMILY FOUNDATION The RAP Bulletin of Biological Assessment is published by: Conservation International 2011 Crystal Drive, Suite 500 Arlington, VA USA 22202 Tel : +1 703-341-2400 www.conservation.org Cover photos: The RAP team surveyed the Grensgebergte Mountains and Upper Palumeu Watershed, as well as the Middle Palumeu River and Kasikasima Mountains visible here. Freshwater resources originating here are vital for all of Suriname. (T. Larsen) Glass frogs (Hyalinobatrachium cf. taylori) lay their -
Worksheets and Post-Lab Activities for “Floating Fishes”
Worksheets and post-lab activities for “Floating Fishes” Possible lesson outlines of this modular activity: This is the lesson as currently written. It begins with the physics of buoyancy before transitioning to fish biology and how it’s related to fisheries Activity Time required 1 Introduction and background 50 min 2 Boat Sinking Lab 50 min 3 Fish Buoyancy 50 min 4 Fishing expedition 50 min An alternative is to start with the fishing expedition in order to emphasize the ecological aspects. Activity Time required 1 Introduction and background 50 min 2 Fishing expedition 50 min 3 Boat Sinking Lab 50 min 4 Fish Buoyancy 50 min If an instructor is short on time and wishes to emphasize the interaction between biology and physics, they can omit the fisheries background. This could be completed within a 3-hr lab period. To save 50 minutes, one can also omit the boat sinking lab. Activity Time required 1 Introduction (omit information about overfishing) 30 min 2 Boat Sinking Lab 50 min 3 Fish Buoyancy 50 min Page 1 of 10 Worksheets and post-lab activities for “Floating Fishes” Sample Worksheet for Day 2: Boat Sinking Lab 1) Add marbles to your boat one by one. What is happening to your boat as you add more marbles?__Students will find that the marbles all roll to one side ______ How many marbles did it take to sink your boat? ______ answers will vary ______________ 2) Take out the marbles and add the first divider to your boat. Add one marble at a time to just one side of your boat. -
Biotechnology
African Journal of Biotechnology Volume 13 Number 15, 9 April, 2014 ISSN 1684-5315 ABOUT AJB The African Journal of Biotechnology (AJB) (ISSN 1684-5315) is published weekly (one volume per year) by Academic Journals. African Journal of Biotechnology (AJB), a new broad-based journal, is an open access journal that was founded on two key tenets: To publish the most exciting research in all areas of applied biochemistry, industrial microbiology, molecular biology, genomics and proteomics, food and agricultural technologies, and metabolic engineering. Secondly, to provide the most rapid turn-around time possible for reviewing and publishing, and to disseminate the articles freely for teaching and reference purposes. All articles published in AJB are peer- reviewed. Submission of Manuscript Please read the Instructions for Authors before submitting your manuscript. The manuscript files should be given the last name of the first author Click here to Submit manuscripts online If you have any difficulty using the online submission system, kindly submit via this email [email protected]. With questions or concerns, please contact the Editorial Office at [email protected]. Editor-In-Chief Associate Editors George Nkem Ude, Ph.D Prof. Dr. AE Aboulata Plant Breeder & Molecular Biologist Plant Path. Res. Inst., ARC, POBox 12619, Giza, Egypt Department of Natural Sciences 30 D, El-Karama St., Alf Maskan, P.O. Box 1567, Crawford Building, Rm 003A Ain Shams, Cairo, Bowie State University Egypt 14000 Jericho Park Road Bowie, MD 20715, USA Dr. S.K Das Department of Applied Chemistry and Biotechnology, University of Fukui, Japan Editor Prof. Okoh, A. I. N.