Hydrological, Environmental and Taxonomical Heterogeneity During the Transition from Drying to Flowing Conditions in a Mediterranean Intermittent River
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Intermittent Rivers and Ephemeral Streams
Intermittent Rivers and Ephemeral Streams: A Unique Biome With Important Contributions to Biodiversity and Ecosystem Services Ross Vander Vorste, University of Wisconsin La Crosse, La Crosse, WI, United States Romain Sarremejane, School of Science and Technology, Nottingham Trent University, Nottingham, United Kingdom Thibault Datry, IRSTEA, UR-Riverly, Centre de Lyon-Villeurbanne, Villeurbanne, France © 2019 Elsevier Inc. All rights reserved. What Are Intermittent Rivers and Ephemeral Streams? 1 Hydrologically Diverse and Globally Abundant 1 Three-in-One: IRES Contribute to Lotic, Lentic, and Terrestrial Dynamics 2 Biogeochemical Dynamics in Intermittent Rivers and Ephemeral Streams 3 Biodiversity in Intermittent Rivers and Ephemeral Streams 4 From Microbes to Elephants, IRES Support High Biodiversity 4 Strategies for Persistence in IRES 6 Organization of Metacommunities Within IRES 6 Management of Intermittent Rivers and Ephemeral Streams 7 Ecosystem Services Provided by IRES 7 Protection and Management of IRES 7 Future of IRES and Global Change 7 Summary 8 References 9 Abstract The majority of flowing waterbodies throughout the world can be considered intermittent rivers or ephemeral streams (IRES) because at some point in time and space they stop flowing or dry. Despite their global abundance, less is known about this biome compared to perennial—permanently flowing—rivers. However, a recent surge in research has dramatically improved our understanding of how IRES function and what types of biodiversity and ecosystem services they support. A cycle of terrestrial-aquatic habitat conditions caused by the periodic drying and rewetting creates a high temporal dynamic in the biogeochemistry, biodiversity, and ecosystem services of IRES. Vast amounts of accumulated sediment, organic matter and organisms can be transported from IRES downstream to larger rivers or lakes, contributing to the global C cycle. -
Hull Fouling Is a Risk Factor for Intercontinental Species Exchange in Aquatic Ecosystems
Aquatic Invasions (2007) Volume 2, Issue 2: 121-131 Open Access doi: http://dx.doi.org/10.3391/ai.2007.2.2.7 © 2007 The Author(s). Journal compilation © 2007 REABIC Research Article Hull fouling is a risk factor for intercontinental species exchange in aquatic ecosystems John M. Drake1,2* and David M. Lodge1,2 1Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556 USA 2Environmental National Center for Ecological Analysis and Synthesis, 735 State Street, Suite 300, Santa Barbara, CA 93101 USA *Corresponding author Current address: Institute of Ecology, University of Georgia, Athens, GA 30602 USA E-mail: [email protected] (JMD) Received: 13 March 2007 / Accepted: 25 May 2007 Abstract Anthropogenic biological invasions are a leading threat to aquatic biodiversity in marine, estuarine, and freshwater ecosystems worldwide. Ballast water discharged from transoceanic ships is commonly believed to be the dominant pathway for species introduction and is therefore increasingly subject to domestic and international regulation. However, compared to species introductions from ballast, translocation by biofouling of ships’ exposed surfaces has been poorly quantified. We report translocation of species by a transoceanic bulk carrier intercepted in the North American Great Lakes in fall 2001. We collected 944 individuals of at least 74 distinct freshwater and marine taxa. Eight of 29 taxa identified to species have never been observed in the Great Lakes. Employing five different statistical techniques, we estimated that the biofouling community of this ship comprised from 100 to 200 species. These findings adjust upward by an order of magnitude the number of species collected from a single ship. -
Georgia Water Quality
GEORGIA SURFACE WATER AND GROUNDWATER QUALITY MONITORING AND ASSESSMENT STRATEGY Okefenokee Swamp, Georgia PHOTO: Kathy Methier Georgia Department of Natural Resources Environmental Protection Division Watershed Protection Branch 2 Martin Luther King Jr. Drive Suite 1152, East Tower Atlanta, GA 30334 GEORGIA SURFACE WATER AND GROUND WATER QUALITY MONITORING AND ASSESSMENT STRATEGY 2015 Update PREFACE The Georgia Environmental Protection Division (GAEPD) of the Department of Natural Resources (DNR) developed this document entitled “Georgia Surface Water and Groundwater Quality Monitoring and Assessment Strategy”. As a part of the State’s Water Quality Management Program, this report focuses on the GAEPD’s water quality monitoring efforts to address key elements identified by the U.S. Environmental Protection Agency (USEPA) monitoring strategy guidance entitled “Elements of a State Monitoring and Assessment Program, March 2003”. This report updates the State’s water quality monitoring strategy as required by the USEPA’s regulations addressing water management plans of the Clean Water Act, Section 106(e)(1). Georgia Department of Natural Resources Environmental Protection Division Watershed Protection Branch 2 Martin Luther King Jr. Drive Suite 1152, East Tower Atlanta, GA 30334 GEORGIA SURFACE WATER AND GROUND WATER QUALITY MONITORING AND ASSESSMENT STRATEGY 2015 Update TABLE OF CONTENTS TABLE OF CONTENTS .............................................................................................. 1 INTRODUCTION......................................................................................................... -
THE WATER QUALITY of the LITTLE COLORADO RIVER WATERSHED Fiscal Year 2007
THE WATER QUALITY OF THE LITTLE COLORADO RIVER WATERSHED Fiscal Year 2007 Prepared by the Surface Water Section March 2009 Publication Number OFR 09-11 LCR REPORT FY 2007 THE WATER QUALITY OF THE LITTLE COLORADO RIVER WATERSHED Fiscal Year 2007 By The Monitoring and Assessments Units Edited by Jason Jones and Meghan Smart Arizona Department of Environmental Quality ADEQ Water Quality Division Surface Water Section Monitoring Unit, Standards & Assessment Unit 1110 West Washington St. Phoenix, Arizona 85007-2935 ii LCR REPORT FY 2007 THANKS: Field Assistance: Anel Avila, Justin Bern, Aiko Condon, Kurt Ehrenburg, Karyn Hanson, Lee Johnson, Jason Jones, Lin Lawson, Sam Rector, Patti Spindler, Meghan Smart, and John Woods. Report Review: Kurt Ehrenburg, Lin Lawson, and Patti Spindler. Report Cover: From left to right: EMAP team including ADEQ, AZGF, and USGS; Rainbow over the Round Valley in the White Mountains; Measuring Tape, and Clear Creek located east of Payson. iii LCR REPORT FY 2007 ABBREVIATIONS Abbreviation Name Abbreviation Name ALKCACO3 Total Alkalinity SO4-T Sulfate Total ALKPHEN Phenolphthalein Alkalinity SPCOND Specific Conductivity Arizona Department of Suspended Sediment AQEQ Environmental Quality SSC Concentration AS-D Arsenic Dissolved su Standard pH Units AS-T Arsenic Total TDS Total Dissolved Solids Arizona Game and Fish AZGF Department TEMP-AIR Air Temperature Arizona Pollutant Discharge TEMP- AZPDES Elimination System WATER Water Temperature BA-D Barium Dissolved TKN Total Kjeldahl Nitrogen B-T Boron Total TMDL Total Maximum Daily Load CA-T Calcium Total USGS U.S. Geological Survey CFS Cubic Feet per Second ZN-D Zinc Dissolved CO3 Carbonate ZN-T Zinc Total CU-TRACE Copper Trace Metal CWA Clean Water Act DO-MGL Dissolved Oxygen in mg/l DO- PERCENT Dissolved Oxygen in Percent E. -
Volume 2, Chapter 10-1: Arthropods: Crustacea
Glime, J. M. 2017. Arthropods: Crustacea – Copepoda and Cladocera. Chapt. 10-1. In: Glime, J. M. Bryophyte Ecology. Volume 2. 10-1-1 Bryological Interaction. Ebook sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 19 July 2020 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology2/>. CHAPTER 10-1 ARTHROPODS: CRUSTACEA – COPEPODA AND CLADOCERA TABLE OF CONTENTS SUBPHYLUM CRUSTACEA ......................................................................................................................... 10-1-2 Reproduction .............................................................................................................................................. 10-1-3 Dispersal .................................................................................................................................................... 10-1-3 Habitat Fragmentation ................................................................................................................................ 10-1-3 Habitat Importance ..................................................................................................................................... 10-1-3 Terrestrial ............................................................................................................................................ 10-1-3 Peatlands ............................................................................................................................................. 10-1-4 Springs ............................................................................................................................................... -
Cladocera (Crustacea: Branchiopoda) of the South-East of the Korean Peninsula, with Twenty New Records for Korea*
Zootaxa 3368: 50–90 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2012 · Magnolia Press ISSN 1175-5334 (online edition) Cladocera (Crustacea: Branchiopoda) of the south-east of the Korean Peninsula, with twenty new records for Korea* ALEXEY A. KOTOV1,2, HYUN GI JEONG2 & WONCHOEL LEE2 1 A. N. Severtsov Institute of Ecology and Evolution, Leninsky Prospect 33, Moscow 119071, Russia E-mail: [email protected] 2 Department of Life Science, Hanyang University, Seoul 133-791, Republic of Korea *In: Karanovic, T. & Lee, W. (Eds) (2012) Biodiversity of Invertebrates in Korea. Zootaxa, 3368, 1–304. Abstract We studied the cladocerans from 15 different freshwater bodies in south-east of the Korean Peninsula. Twenty species are first records for Korea, viz. 1. Sida ortiva Korovchinsky, 1979; 2. Pseudosida cf. szalayi (Daday, 1898); 3. Scapholeberis kingi Sars, 1888; 4. Simocephalus congener (Koch, 1841); 5. Moinodaphnia macleayi (King, 1853); 6. Ilyocryptus cune- atus Štifter, 1988; 7. Ilyocryptus cf. raridentatus Smirnov, 1989; 8. Ilyocryptus spinifer Herrick, 1882; 9. Macrothrix pen- nigera Shen, Sung & Chen, 1961; 10. Macrothrix triserialis Brady, 1886; 11. Bosmina (Sinobosmina) fatalis Burckhardt, 1924; 12. Chydorus irinae Smirnov & Sheveleva, 2010; 13. Disparalona ikarus Kotov & Sinev, 2011; 14. Ephemeroporus cf. barroisi (Richard, 1894); 15. Camptocercus uncinatus Smirnov, 1971; 16. Camptocercus vietnamensis Than, 1980; 17. Kurzia (Rostrokurzia) longirostris (Daday, 1898); 18. Leydigia (Neoleydigia) acanthocercoides (Fischer, 1854); 19. Monospilus daedalus Kotov & Sinev, 2011; 20. Nedorchynchotalona chiangi Kotov & Sinev, 2011. Most of them are il- lustrated and briefly redescribed from newly collected material. We also provide illustrations of four taxa previously re- corded from Korea: Sida crystallina (O.F. -
Diversity and Abundance of Cladoceran Zooplankton in Wular Lake, Kashmir Himalaya
Research Journal of Environmental and Earth Sciences 5(7): 410-417, 2013 ISSN: 2041-0484; e-ISSN: 2041-0492 © Maxwell Scientific Organization, 2013 Submitted: April 17, 2013 Accepted: May 03, 2013 Published: July 20, 2013 Diversity and Abundance of Cladoceran Zooplankton in Wular Lake, Kashmir Himalaya Javaid Ahmad Shah and Ashok K. Pandit Aquatic Ecology Laboratory, Centre of Research for Development, University of Kashmir 190006, J&K (India) Abstract: The present study was carried out on Wular lake, the largest freshwater lake of India to obtain a baseline data on the dynamics of species composition and density of cladoceran zooplankton for the period of one year from September 2010 to August 2011 at five different study sites. Investigations revealed about 23 species of Cladocera belonging to six families were reported during the entire study. Among the six families, Chydoridae was numerically dominant, being represented by nine species, followed by Daphnidae with seven species, Bosminidae, Moinidae and Sididae with two species each and Macrothricidae with only one species. Shannon index was noticed highest for site III reflecting the stable environmental conditions of this biotope. Keywords: Chydoridae, Cladocera, Daphnidae, Himalaya, Kashmir, Wular INTRODUCTION is, therefore, aimed to collate a baseline data on the cladoceran community of Wular lake in terms of Zooplankton holds a central position in the food spatial and temporal variations in species chain of most of the lakes, reservoirs and ponds and are composition and abundance by using various highly sensitive to environmental variations which as a diversity indices. result bring changes in their abundance, species diversity or community composition, because most Study area: Wular lake the largest freshwater lake of species have short generation time (Pandit, 1980; India, is situated at an altitude of 1580 m (a. -
Factors Controlling Zooplankton Dynamics in a Subtropical Lake During Cyanobacterial Bloom Events
FACTORS CONTROLLING ZOOPLANKTON DYNAMICS IN A SUBTROPICAL LAKE DURING CYANOBACTERIAL BLOOM EVENTS By AKEAPOT SRIFA A THESIS PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE UNIVERSITY OF FLORIDA 2010 1 © 2010 Akeapot Srifa 2 To my parents, my role models in diligence and positive thinking 3 ACKNOWLEDGMENTS First of all, I would like to express my most sincere gratitude to my supervisor, Professor Edward J. Phlips, for his ceaseless academic dedication during my graduate study in the University of Florida. He has willingly supported me from the beginning in academia and provided excellent research experiences during the past two years. I would like to express my most sincere to other supervisory committee members, Professor Karl E. Havens and Professor Mark Brenner, for sharing me their professional research excellence, and for giving me invaluable and constructive suggestions and comments to the research I made during my study. I would like to gratefully acknowledge Professor Charles E. Cichra and Mary Cichra for their generosity and dedications in the academic supports and guidance. Without the supports from them, this research would not have been completed. My special thanks also extend to Dr. Mete Yilmaz for his invaluable help and suggestions in professional laboratory skills, Dr. Lance Riley for his captaincy on the research vessel, Don O’steen and Linghan Dong for their helps in sampling sessions, Dorota Roth and Joey Chait for their help in sample analyses, Amanda Croteau and Brittany Baugher for their help in the identification of microscopic zooplankton, my colleagues Nikki Dix, Loren Mathews, and Paula Viveros for their kind help throughout my laboratory works as well as academic skills. -
Genetic Population Structure of the Fairy Shrimp Branchinecta Coloradensis (Anostraca) in the Rocky Mountains of Colorado
Color profile: Disabled Composite Default screen 2049 Genetic population structure of the fairy shrimp Branchinecta coloradensis (Anostraca) in the Rocky Mountains of Colorado Andrew J. Bohonak Abstract: Dispersal rates for freshwater invertebrates are often inferred from population genetic data. Although genetic approaches can indicate the amount of isolation in natural populations, departures from an equilibrium between drift and gene flow often lead to biased gene flow estimates. I investigated the genetic population structure of the pond- dwelling fairy shrimp Branchinecta coloradensis in the Rocky Mountains of Colorado, U.S.A., using allozymes. Glaciation in this area and the availability of direct dispersal estimates from previous work permit inferences regarding the relative impacts of history and contemporary gene flow on population structure. Hierarchical F statistics were used θ θ to quantify differentiation within and between valleys ( SV and VT, respectively). Between valleys separated by 5– θ 10 km, a high degree of differentiation ( VT = 0.77) corresponds to biologically reasonable gene flow estimates of 0.07 individuals per generation, although it is possible that this value represents founder effects and nonequilibrium ≤ θ conditions. On a local scale ( 110 m), populations are genetically similar ( SV = 0.13) and gene flow is estimated to be 1.7 individuals exchanged between ponds each generation. This is very close to an ecological estimate of dispersal for B. coloradensis via salamanders. Gene flow estimates from previous studies on other Anostraca are also similar on comparable geographic scales. Thus, population structure in B. coloradensis appears to be at or near equilibrium on a local scale, and possibly on a regional scale as well. -
Classification Scheme of Freshwater Aquatic Organisms Freshwater Keys: Classification
Compendium of Recommended Keys for British Columbia Freshwater Organisms: Part 3 Classification Scheme of Freshwater Aquatic Organisms Freshwater Keys: Classification Table of Contents TABLE OF CONTENTS.............................................................................................................................. 2 INTRODUCTION......................................................................................................................................... 4 KINGDOM MONERA................................................................................................................................. 5 KINGDOM PROTISTA............................................................................................................................... 5 KINGDOM FUNGI ...................................................................................................................................... 5 KINGDOM PLANTAE ................................................................................................................................ 6 KINGDOM ANIMALIA .............................................................................................................................. 8 SUBKINGDOM PARAZOA ........................................................................................................................ 8 SUBKINGDOM EUMETAZOA.................................................................................................................. 8 2 Freshwater Keys: Classification 3 Freshwater Keys: Classification -
September 2, 2021
September 2, 2021 Via www.regulations.gov The Honorable Michael Regan The Honorable Jaime A. Pinkham Administrator Acting Assistant Secretary of the Army for U.S. Environmental Protection Agency Civil Works 1200 Pennsylvania Avenue NW Department of the Army Washington, DC 20460 108 Army Pentagon Washington, DC 20310 Mr. John Goodin Director Mr. Vance F. Stewart III Office of Wetlands, Oceans and Watersheds Acting Principal Deputy U.S. Environmental Protection Agency Office of the Assistant Secretary of the 1200 Pennsylvania Avenue NW Army for Civil Works Washington, DC 20460 Department of the Army 108 Army Pentagon Washington, DC 20310 Re: Request for Recommendations on Defining “Waters of the United States” Docket No. EPA-HQ-OW-2021-03281 Dear Administrator Regan, Acting Assistant Secretary Pinkham, Mr. Goodin, and Mr. Stewart: Together, our 85 organizations write to ask you to take two steps to protect critical wetlands, streams, and other waters that we and our millions of members rely on for swimming, fishing, boating, drinking water, and our livelihoods. First, we urge the U.S. Environmental Protection Agency (“EPA”) and U.S. Army Corps of Engineers (“Corps”) (together, the “Agencies”) to promptly restore and implement the regulatory framework in effect prior to the so-called Navigable Waters Protection Rule (“NWPR”). Second, we urge the Agencies to promulgate a new definition of “waters of the United States” that is rooted in science, consistent with Supreme Court precedent, and faithful to the objective of the Clean Water Act. -
WATER QUALITY in GEORGIA 2016-2017 (2018 Integrated 305B/303D Report)
WATER QUALITY IN GEORGIA 2016-2017 (2018 Integrated 305b/303d Report) WATER QUALITY IN GEORGIA Georgia Department of Natural Resources Environmental Protection Division WATER QUALITY IN GEORGIA 2016-2017 (2018 Integrated 305b/303d Report) Preface This report was prepared by the Georgia Environmental Protection Division (EPD), Department of Natural Resources, as required by Section 305(b) of Public Law 92-500 (the Clean Water Act) and as a public information document. It represents a synoptic extraction of the EPD files and, in certain cases, information has been presented in summary form from those files. The reader is therefore advised to use this condensed information with the knowledge that it is a summary document and more detailed information may be available in EPD files. This report covers a two-year period, January 1, 2016 through December 31, 2017. Comments or questions related to the content of this report are invited and should be addressed to: Environmental Protection Division Georgia Department of Natural Resources Watershed Protection Branch 2 Martin Luther King, Jr. Drive, SE Suite 1162 East Tower Atlanta, Georgia 30334 WATER QUALITY IN GEORGIA This page is intentionally blank. WATER QUALITY IN GEORGIA CHAPTER 1 Watershed Protection in Georgia The GAEPD is a comprehensive environmental agency Executive Summary responsible for environmental protection, management, regulation, permitting, and Purpose This report, Water Quality in Georgia, enforcement in Georgia. The GAEPD has for 2016-20172016-2017, was prepared by the many years aggressively sought most available Georgia Environmental Protection Division program delegations from the USEPA in order to (EPD) of the Department of Natural Resources achieve and maintain a coordinated, integrated (DNR).