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Historical Volcanism and the State of Stress in the East African Rift System
Historical volcanism and the state of stress in the East African Rift System Article Accepted Version Open Access Wadge, G., Biggs, J., Lloyd, R. and Kendall, J.-M. (2016) Historical volcanism and the state of stress in the East African Rift System. Frontiers in Earth Science, 4. 86. ISSN 2296- 6463 doi: https://doi.org/10.3389/feart.2016.00086 Available at http://centaur.reading.ac.uk/66786/ It is advisable to refer to the publisher’s version if you intend to cite from the work. See Guidance on citing . To link to this article DOI: http://dx.doi.org/10.3389/feart.2016.00086 Publisher: Frontiers media All outputs in CentAUR are protected by Intellectual Property Rights law, including copyright law. Copyright and IPR is retained by the creators or other copyright holders. Terms and conditions for use of this material are defined in the End User Agreement . www.reading.ac.uk/centaur CentAUR Central Archive at the University of Reading Reading’s research outputs online 1 Historical volcanism and the state of stress in the East African 2 Rift System 3 4 5 G. Wadge1*, J. Biggs2, R. Lloyd2, J-M. Kendall2 6 7 8 1.COMET, Department of Meteorology, University of Reading, Reading, UK 9 2.COMET, School of Earth Sciences, University of Bristol, Bristol, UK 10 11 * [email protected] 12 13 14 Keywords: crustal stress, historical eruptions, East African Rift, oblique motion, 15 eruption dynamics 16 17 18 19 20 21 Abstract 22 23 Crustal extension at the East African Rift System (EARS) should, as a tectonic ideal, 24 involve a stress field in which the direction of minimum horizontal stress is 25 perpendicular to the rift. -
12146361 02.Pdf
Proposed Development Plans Water Supply Development Plan Urban Water Supply Development (32 Urban Centers) 1) Rehabilitation (30 UC) 699,000 m3/day 2) Expansion (29 UC) 1,542,000 m3/day 3) New Construction (2 UC) 19,000 m3/day 4) Service Population 17.01 million Rural Water Supply (10 Counties) 1) Large Scale 209,000 m3/day 2) Small Scale 110,000 m3/day 3) Target Population 4.04 million Sanitation Development Plan Sewerage Development (25 Urban Centers) 1) Rehabilitation (6 UC) 244,000 m3/day 2) Expansion (6 UC) 715,000 m3/day 3) New Construction (19 UC) 430,000 m3/day 4) Service Population 16.26 million On-site Sanitation (10 Counties) 1) Installation of Proper On-site Sanitation Facilities by Individual or Communities 2) Target Population 4.28 million Irrigation Development Plan Large Scale Irrigation Area 1) Large Scale Irrigation 37,280 ha (4 Projects) MA -MA F - 33 2) Small Scale Irrigation 6,484 ha (10 Counties) 3) Private Sector Irrigation 2,344 ha (10 Counties) P Hydropower Development Plan 1) Munyu Multipurpose Dam Project 40MW 2) Thwake Multipurpose Dam Project 20MW Water Resources Development Plan 1) Storage Dams 16 nos. (1,689 MCM) 2) Small Storage Dams and 1,880 nos. Pans (94 MCM) 3) Boreholes 350 nos. (35 MCM/year) 4) Inter-basin Transfer 168 MCM/year (from Tana CA to Nairobi, Ext.) 5) Intra-basin Transfer 37 MCM/year (from Mzima Spring to Mombasa/Kwale/Ukunda, Ext.) 6) Intra-basin Transfer 31 MCM/year (from Athi R. to Mombasa/ Malindi/Kilifi/Mtwapa, Ext.) 7) Desalination for Mombasa 93 MCM/year LEGEND Dam(Existing) Water -
Phylogenetic Relationships Within the Speciose Family Characidae
Oliveira et al. BMC Evolutionary Biology 2011, 11:275 http://www.biomedcentral.com/1471-2148/11/275 RESEARCH ARTICLE Open Access Phylogenetic relationships within the speciose family Characidae (Teleostei: Ostariophysi: Characiformes) based on multilocus analysis and extensive ingroup sampling Claudio Oliveira1*, Gleisy S Avelino1, Kelly T Abe1, Tatiane C Mariguela1, Ricardo C Benine1, Guillermo Ortí2, Richard P Vari3 and Ricardo M Corrêa e Castro4 Abstract Background: With nearly 1,100 species, the fish family Characidae represents more than half of the species of Characiformes, and is a key component of Neotropical freshwater ecosystems. The composition, phylogeny, and classification of Characidae is currently uncertain, despite significant efforts based on analysis of morphological and molecular data. No consensus about the monophyly of this group or its position within the order Characiformes has been reached, challenged by the fact that many key studies to date have non-overlapping taxonomic representation and focus only on subsets of this diversity. Results: In the present study we propose a new definition of the family Characidae and a hypothesis of relationships for the Characiformes based on phylogenetic analysis of DNA sequences of two mitochondrial and three nuclear genes (4,680 base pairs). The sequences were obtained from 211 samples representing 166 genera distributed among all 18 recognized families in the order Characiformes, all 14 recognized subfamilies in the Characidae, plus 56 of the genera so far considered incertae sedis in the Characidae. The phylogeny obtained is robust, with most lineages significantly supported by posterior probabilities in Bayesian analysis, and high bootstrap values from maximum likelihood and parsimony analyses. -
Implications for Management AFRICAN GREAT LAKES
AFRICAN GREAT LAKES CONFERENCE 2nd – 5th MAY 2017, ENTEBBE, UGANDA Dynamics of Fish Stocks of Commercial Importance in Lake Victoria, East Africa: Implications for Management Robert Kayanda, Anton Taabu-Munyaho, Dismas Mbabazi, Hillary Mrosso, and Chrisphine Nyamweya INTRODUCTION • Lake Victoria with a surface area of 68,800 sqkm is the world’s second largest freshwater body • It supports one of the world’s most productive inland fisheries with the estimated total fish landings from the lake for the period of 2011 to 2014 have been about 1 million tons with a beach value increasing from about US$ 550 Million in 2011 to about US$ 840 million in 2014. • It supports about 220,000 fishers (Frame Survey 2016) • The fish stocks of Lake Victoria have changed dramatically since the introduction of Nile perch Lates niloticus during the late 1950s and early 1960s Fishery Haplochromines The Original Fish Fauna Brycinus sp Protopterus Rastrineobola Mormyrus spp Barbus spp Bagrus docmac Labeo Schilbe intermedius Oreochromis variabilis Clarias gariepinus Mormyrus spp Synodontis victoriae Oreochromis leucostictus INTRODUCTION Currently, the fisheries is dominated by four major commercial important species, these are; •Nile perch •Dagaa •Nile tilapia •Haplochromis Apart from Nile tilapia only estimated through trawl and catch surveys, the other 3 are estimated through trawl, acoustics, and catch INTRODUCTION This paper summarizes current knowledge of the status of the fish stocks and reviews the need for species specific management plans for the major commercial important fish species of Lake Victoria (Nile perch, Nile tilapia, dagaa and haplochromines). Methods • Fisheries dependent – Frame surveys – Catch assessment surveys • Fisheries independent – Acoustic – Bottom trawl Biomass and relative abundance • Total biomass from the surveys 3500 remained fairly stable over time. -
Fish, Various Invertebrates
Zambezi Basin Wetlands Volume II : Chapters 7 - 11 - Contents i Back to links page CONTENTS VOLUME II Technical Reviews Page CHAPTER 7 : FRESHWATER FISHES .............................. 393 7.1 Introduction .................................................................... 393 7.2 The origin and zoogeography of Zambezian fishes ....... 393 7.3 Ichthyological regions of the Zambezi .......................... 404 7.4 Threats to biodiversity ................................................... 416 7.5 Wetlands of special interest .......................................... 432 7.6 Conservation and future directions ............................... 440 7.7 References ..................................................................... 443 TABLE 7.2: The fishes of the Zambezi River system .............. 449 APPENDIX 7.1 : Zambezi Delta Survey .................................. 461 CHAPTER 8 : FRESHWATER MOLLUSCS ................... 487 8.1 Introduction ................................................................. 487 8.2 Literature review ......................................................... 488 8.3 The Zambezi River basin ............................................ 489 8.4 The Molluscan fauna .................................................. 491 8.5 Biogeography ............................................................... 508 8.6 Biomphalaria, Bulinis and Schistosomiasis ................ 515 8.7 Conservation ................................................................ 516 8.8 Further investigations ................................................. -
Hemichromis Bimaculatus (African Jewelfish)
African Jewelfish (Hemichromis bimaculatus) Ecological Risk Screening Summary U.S. Fish and Wildlife Service, April 2011 Revised, September 2018 Web Version, 2/14/2019 Photo: Zhyla. Licensed under CC BY-SA 3.0. Available: https://commons.wikimedia.org/wiki/File:Hemichromis_bimaculatus1.jpg. (September 2018). 1 Native Range and Status in the United States Native Range From Froese and Pauly (2018): “Africa: widely distributed in West Africa, where it is known from most hydrographic basins [Teugels and Thys van den Audenaerde 2003], associated with forested biotopes [Daget and Teugels 1991, Lamboj 2004]. Also reported from coastal basins of Cameroon, Democratic Republic of the Congo and Nile basin [Teugels and Thys van den Audenaerde 1992], but at least its presence in Cameroon is unconfirmed in [Stiassny et al. 2008]. [Lamboj 2004] limits this species to Guinea, Sierra Leone and Liberia.” 1 From Azeroual and Lalèyè (2010): “This species is widely distributed throughout western Africa, but has also been recorded from Algeria to Egypt.” “Northern Africa: Within this region this species is very rare. It used to be caught from the coastal lagoons, especially Lake Mariut (Egypt) and Algeria. Its [sic] found in Tunisia in the wadis of Kebili in the south of Tunisia and in wadis near Chott Melrhir in eastern Algeria (Kraiem, pers. comm.), and Egypt (Wadi El Rayan Lakes).” “Western Africa: It is known from most hydrographic basins in western Africa.” Status in the United States It is not certain if this species is present in the United States, or if records pertain to H. letourneuxi. From NatureServe (2018): “Introduced and established in Dade County, Florida, […] (Nelson 1983).” From Nico et al. -
Joint Geophysical Data Analysis for Geothermal Energy Exploration Antony Munika Wamalwa University of Texas at El Paso, [email protected]
University of Texas at El Paso DigitalCommons@UTEP Open Access Theses & Dissertations 2011-01-01 Joint Geophysical Data Analysis For Geothermal Energy Exploration Antony Munika Wamalwa University of Texas at El Paso, [email protected] Follow this and additional works at: https://digitalcommons.utep.edu/open_etd Part of the Geophysics and Seismology Commons, and the Oil, Gas, and Energy Commons Recommended Citation Wamalwa, Antony Munika, "Joint Geophysical Data Analysis For Geothermal Energy Exploration" (2011). Open Access Theses & Dissertations. 2414. https://digitalcommons.utep.edu/open_etd/2414 This is brought to you for free and open access by DigitalCommons@UTEP. It has been accepted for inclusion in Open Access Theses & Dissertations by an authorized administrator of DigitalCommons@UTEP. For more information, please contact [email protected]. JOINT GEOPHYSICAL DATA ANALYSIS FOR GEOTHERMAL ENERGY EXPLORATION ANTONY MUNIKA WAMALWA Department of Geological Sciences APPROVED: ___________________________ Laura Serpa, Ph.D., Chair ___________________________ Elizabeth Anthony, Ph.D. ___________________________ Diane Doser, Ph.D. ___________________________ Aaron Velasco, Ph.D. ___________________________ Kevin Mickus, Ph.D. _________________________ Benjamin C. Flores, Ph.D. Acting Dean of the Graduate School Copyright © Antony Munika Wamalwa 2011 JOINT GEOPHYSICAL DATA ANALYSIS FOR GEOTHERMAL ENERGY EXPLORATION by ANTONY MUNIKA WAMALWA, M.S., B.S. DISSERTATION Presented to the Faculty of the Graduate School of The University of Texas at El Paso in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY Department of Geological Sciences THE UNIVERSITY OF TEXAS AT EL PASO December 2011 Acknowledgements Many people helped in making this study a success. Although I may not mention all of them here dues to limited space, I would like to extend my gratitude to Dr. -
Croaking Gourami, Trichopsis Vittata (Cuvier, 1831), in Florida, USA
BioInvasions Records (2013) Volume 2, Issue 3: 247–251 Open Access doi: http://dx.doi.org/10.3391/bir.2013.2.3.12 © 2013 The Author(s). Journal compilation © 2013 REABIC Rapid Communication Croaking gourami, Trichopsis vittata (Cuvier, 1831), in Florida, USA Pamela J. Schofield 1* and Darren J. Pecora2 1 US Geological Survey, Southeast Ecological Science Center, 7920 NW 71st Street, Gainesville, FL 32653, USA 2 US Fish and Wildlife Service, Arthur R. Marshall Loxahatchee National Wildlife Refuge, 10216 Lee Road, Boynton Beach, FL 33473, USA E-mail: [email protected] (PJS), [email protected] (DJP) *Corresponding author Received: 8 February 2013 / Accepted: 30 May 2013 / Published online: 1 July 2013 Handling editor: Kit Magellan Abstract The croaking gourami, Trichopsis vittata, is documented from wetland habitats in southern Florida. This species was previously recorded from the same area over 15 years ago, but was considered extirpated. The rediscovery of a reproducing population of this species highlights the dearth of information available regarding the dozens of non-native fishes in Florida, as well as the need for additional research and monitoring. Key words: canal; croaking gourami; cypress swamp; Florida; Loxahatchee; Osphronemidae; Trichopsis vittata was previously considered extirpated (Shafland Introduction et al. 2008a, b), but is now known to be reproducing in a localised area. Dozens of non-native fishes have been introduced into Florida’s inland waterways, via accidental escape, pet releases, or intentional introduction -
Alcolapia Grahami ERSS
Lake Magadi Tilapia (Alcolapia grahami) Ecological Risk Screening Summary U.S. Fish & Wildlife Service, March 2015 Revised, August 2017, October 2017 Web Version, 8/21/2018 1 Native Range and Status in the United States Native Range From Bayona and Akinyi (2006): “The natural range of this species is restricted to a single location: Lake Magadi [Kenya].” Status in the United States No records of Alcolapia grahami in the wild or in trade in the United States were found. The Florida Fish and Wildlife Conservation Commission has listed the tilapia Alcolapia grahami as a prohibited species. Prohibited nonnative species (FFWCC 2018), “are considered to be dangerous to the ecology and/or the health and welfare of the people of Florida. These species are not allowed to be personally possessed or used for commercial activities.” Means of Introductions in the United States No records of Alcolapia grahami in the United States were found. 1 Remarks From Bayona and Akinyi (2006): “Vulnerable D2 ver 3.1” Various sources use Alcolapia grahami (Eschmeyer et al. 2017) or Oreochromis grahami (ITIS 2017) as the accepted name for this species. Information searches were conducted under both names to ensure completeness of the data gathered. 2 Biology and Ecology Taxonomic Hierarchy and Taxonomic Standing According to Eschmeyer et al. (2017), Alcolapia grahami (Boulenger 1912) is the current valid name for this species. It was originally described as Tilapia grahami; it has also been known as Oreoghromis grahami, and as a synonym, but valid subspecies, of -
Trophic Niche Segregation in the Nilotic Ichthyofauna of Lake Albert (Uganda, Africa)
Environmental Biology of Fishes (2005) 74:247–260 Ó Springer 2005 DOI 10.1007/s10641-005-3190-8 Trophic niche segregation in the Nilotic ichthyofauna of Lake Albert (Uganda, Africa) Linda M. Campbella,d, Sylvester B. Wanderab, Robert J. Thackerc,e, D. George Dixona & Robert E. Heckya aDepartment of Biology, University of Waterloo, 200 University Avenue. Waterloo, Ontario, Canada N2L 3G1 bFisheries Resources Research Institute, P.O. Box 343, Jinja, Uganda cDepartment of Physics and Astronomy, McMaster University, 1280 Main St. W, Hamilton, Ontario, Canada dCurrent address: School of Environmental Studies and Department of Biology, Queen’s University, Kingston, ON, Canada K7L 3N6 (e-mail: [email protected]) eCurrent address: Department of Physics and Astronomy, Queen’s University, Kingston, ON, Canada K7L 3N6 Received 29 April 2004 Accepted 13 February 2005 Key words: d13C, d15N, food webs, Nile perch, stable isotopes Synopsis Nile perch, Lates niloticus, and Nile tilapia, Oreochromis niloticus, were originally transplanted from Lake Albert in western Uganda to the African Great Lakes, Lake Victoria and Lake Kyoga, where they are partially implicated in reduction of the fish species diversity. Lake Albert is facing multiple environmental changes, including declining fish species diversity, hyper-eutrophication, hypoxia, and reduced fish catches. To examine the role of Nile perch and Nile tilapia in the food web in their native Lake Albert, we estimated their diets using stable nitrogen and carbon isotopes. In Lake Albert, the tilapiine congeners (closely related species), Tilapia zillii, Oreochromis leucostictus, and Sarethorodon galilaeus, and the centropomid Nile perch congener, Lates macrophthalmus, have narrower diet breath in the presence of the native O. -
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 ................................................................................................................................ -
A Guide to the Parasites of African Freshwater Fishes
A Guide to the Parasites of African Freshwater Fishes Edited by T. Scholz, M.P.M. Vanhove, N. Smit, Z. Jayasundera & M. Gelnar Volume 18 (2018) Chapter 2.1. FISH DIVERSITY AND ECOLOGY Martin REICHARD Diversity of fshes in Africa Fishes are the most taxonomically diverse group of vertebrates and Africa shares a large portion of this diversity. This is due to its rich geological history – being a part of Gondwana, it shares taxa with the Neotropical region, whereas recent close geographical affnity to Eurasia permitted faunal exchange with European and Asian taxa. At the same time, relative isolation and the complex climatic and geological history of Africa enabled major diversifcation within the continent. The taxonomic diversity of African freshwater fshes is associated with functional and ecological diversity. While freshwater habitats form a tiny fraction of the total surface of aquatic habitats compared with the marine environment, most teleost fsh diversity occurs in fresh waters. There are over 3,200 freshwater fsh species in Africa and it is likely several hundreds of species remain undescribed (Snoeks et al. 2011). This high diversity and endemism is likely mirrored in diversity and endemism of their parasites. African fsh diversity includes an ancient group of air-breathing lungfshes (Protopterus spp.). Other taxa are capable of breathing air and tolerate poor water quality, including several clariid catfshes (e.g., Clarias spp.; Fig. 2.1.1D) and anabantids (Ctenopoma spp.). Africa is also home to several bichir species (Polypterus spp.; Fig. 2.1.1A), an ancient fsh group endemic to Africa, and bonytongue Heterotis niloticus (Cuvier, 1829) (Osteoglossidae), a basal actinopterygian fsh.