Summary of Characteristics of Major African Lakes
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An Analysis of Primary and Secondary Production in Lake Kariba in a Changing Climate
AN ANALYSIS OF PRIMARY AND SECONDARY PRODUCTION IN LAKE KARIBA IN A CHANGING CLIMATE MZIME R. NDEBELE-MURISA A thesis submitted in partial fulfillment of the requirements for the degree of Doctor Philosophiae in the Department of Biodiversity and Conservation Biology, University of the Western Cape Supervisor: Prof. Charles Musil Co-Supervisor: Prof. Lincoln Raitt May 2011 An analysis of primary and secondary production in Lake Kariba in a changing climate Mzime Regina Ndebele-Murisa KEYWORDS Climate warming Limnology Primary production Phytoplankton Zooplankton Kapenta production Lake Kariba i Abstract Title: An analysis of primary and secondary production in Lake Kariba in a changing climate M.R. Ndebele-Murisa PhD, Biodiversity and Conservation Biology Department, University of the Western Cape Analysis of temperature, rainfall and evaporation records over a 44-year period spanning the years 1964 to 2008 indicates changes in the climate around Lake Kariba. Mean annual temperatures have increased by approximately 1.5oC, and pan evaporation rates by about 25%, with rainfall having declined by an average of 27.1 mm since 1964 at an average rate of 6.3 mm per decade. At the same time, lake water temperatures, evaporation rates, and water loss from the lake have increased, which have adversely affected lake water levels, nutrient and thermal dynamics. The most prominent influence of the changing climate on Lake Kariba has been a reduction in the lake water levels, averaging 9.5 m over the past two decades. These are associated with increased warming, reduced rainfall and diminished water and therefore nutrient inflow into the lake. The warmer climate has increased temperatures in the upper layers of lake water, the epilimnion, by an overall average of 1.9°C between 1965 and 2009. -
§4-71-6.5 LIST of CONDITIONALLY APPROVED ANIMALS November
§4-71-6.5 LIST OF CONDITIONALLY APPROVED ANIMALS November 28, 2006 SCIENTIFIC NAME COMMON NAME INVERTEBRATES PHYLUM Annelida CLASS Oligochaeta ORDER Plesiopora FAMILY Tubificidae Tubifex (all species in genus) worm, tubifex PHYLUM Arthropoda CLASS Crustacea ORDER Anostraca FAMILY Artemiidae Artemia (all species in genus) shrimp, brine ORDER Cladocera FAMILY Daphnidae Daphnia (all species in genus) flea, water ORDER Decapoda FAMILY Atelecyclidae Erimacrus isenbeckii crab, horsehair FAMILY Cancridae Cancer antennarius crab, California rock Cancer anthonyi crab, yellowstone Cancer borealis crab, Jonah Cancer magister crab, dungeness Cancer productus crab, rock (red) FAMILY Geryonidae Geryon affinis crab, golden FAMILY Lithodidae Paralithodes camtschatica crab, Alaskan king FAMILY Majidae Chionocetes bairdi crab, snow Chionocetes opilio crab, snow 1 CONDITIONAL ANIMAL LIST §4-71-6.5 SCIENTIFIC NAME COMMON NAME Chionocetes tanneri crab, snow FAMILY Nephropidae Homarus (all species in genus) lobster, true FAMILY Palaemonidae Macrobrachium lar shrimp, freshwater Macrobrachium rosenbergi prawn, giant long-legged FAMILY Palinuridae Jasus (all species in genus) crayfish, saltwater; lobster Panulirus argus lobster, Atlantic spiny Panulirus longipes femoristriga crayfish, saltwater Panulirus pencillatus lobster, spiny FAMILY Portunidae Callinectes sapidus crab, blue Scylla serrata crab, Samoan; serrate, swimming FAMILY Raninidae Ranina ranina crab, spanner; red frog, Hawaiian CLASS Insecta ORDER Coleoptera FAMILY Tenebrionidae Tenebrio molitor mealworm, -
Phylogeny of a Rapidly Evolving Clade: the Cichlid Fishes of Lake Malawi
Proc. Natl. Acad. Sci. USA Vol. 96, pp. 5107–5110, April 1999 Evolution Phylogeny of a rapidly evolving clade: The cichlid fishes of Lake Malawi, East Africa (adaptive radiationysexual selectionyspeciationyamplified fragment length polymorphismylineage sorting) R. C. ALBERTSON,J.A.MARKERT,P.D.DANLEY, AND T. D. KOCHER† Department of Zoology and Program in Genetics, University of New Hampshire, Durham, NH 03824 Communicated by John C. Avise, University of Georgia, Athens, GA, March 12, 1999 (received for review December 17, 1998) ABSTRACT Lake Malawi contains a flock of >500 spe- sponsible for speciation, then we expect that sister taxa will cies of cichlid fish that have evolved from a common ancestor frequently differ in color pattern but not morphology. within the last million years. The rapid diversification of this Most attempts to determine the relationships among cichlid group has been attributed to morphological adaptation and to species have used morphological characters, which may be sexual selection, but the relative timing and importance of prone to convergence (8). Molecular sequences normally these mechanisms is not known. A phylogeny of the group provide the independent estimate of phylogeny needed to infer would help identify the role each mechanism has played in the evolutionary mechanisms. The Lake Malawi cichlids, however, evolution of the flock. Previous attempts to reconstruct the are speciating faster than alleles can become fixed within a relationships among these taxa using molecular methods have species (9, 10). The coalescence of mtDNA haplotypes found been frustrated by the persistence of ancestral polymorphisms within populations predates the origin of many species (11). In within species. -
Cichlid Diversity, Speciation and Systematics: Examples from the Great African Lakes
Cichlid diversity, speciation and systematics: examples from the Great African Lakes Jos Snoeks, Africa Museum, Ichthyology- Cichlid Research Unit, Leuvensesteenweg 13, B-3080 Ter vuren,.Belgium. Tel: (32) 2 769 56 28, Fax: (32) 2 769 56 42(e-mail: [email protected]) ABSTRACT The cichlid faunas of the large East African lakes pro vide many fascina ting research tapies. They are unique because of the large number of species involved and the ir exceptional degree ofendemicity. In addition, certain taxa exhibit a substantial degree of intra~lacustrine endemism. These features al one make the Great African Lakes the largest centers of biodiversity in the vertebrate world. The numbers of cichlid species in these lakes are considered from different angles. A review is given of the data available on the tempo of their speciation, and sorne of the biological implications of its explosive character are discussed. The confusion in the definition of many genera is illustrated and the current methodology of phylogenetic research briefly commented upon. Theresults of the systematic research within the SADC/GEFLake Malawi/NyasaBiodiversity Conservation Project are discussed. It is argued that systematic research on the East African lake cichlids is entering an era of lesser chaos but increasing complexity. INTRODUCTION The main value of the cichlids of the Great African Grea ter awareness of the scientific and economi Lakes is their economie importance as a readily cal value of these fishes has led to the establishment accessible source of protein for the riparian people. In of varioüs recent research projects such as the three addition, these fishes are important to the specialized GEF (Global Environmental Facility) projects on the aquarium trade as one of the more exci ting fish groups larger lakes (Victoria, Tanganyika, Malawi/Nyasa). -
Ein 40 Jahre Alter Traum Wird Wahr – Reise in Den Lake Malawi National Park
DCG_Info_08_2018_HR_20180719_DCG_Info 19.07.2018 17:03 Seite 178 Ein 40 Jahre alter Traum wird wahr – Reise in den Lake Malawi National Park Stefan Pierdzig Abb. 1: Küstenabschnitt südlich Otter Point. Egal, ob nun der Portugiese Cardoso im gendtraum erzählte, ermunterte mich, Der folgende Reisebericht erhebt keine Jahr 1846 oder der Afrikaforscher das Vorhaben in die Tat umzusetzen. Die hochwissenschaftlichen Ansprüche, son- David Livingstone anno 1859 für sich beste aller Ehefrauen gab, voller Ver- dern möchte in Bild und Wort die fan- reklamieren können, als erste Europäer ständnis für mein kühnes Vorhaben, grü- tastischen Eindrücke unter und über den Malawisee erreicht zu haben, beide nes Licht, ich überlegte, was ein gutes Wasser wiedergeben und dem einen ahnten sicherlich nicht, welchen biolo- Ziel am See sein könnte (der Lake Ma- oder anderen Mut machen, seinen eige- gischen Schatz der See in Form seiner lawi National Park), organisierte die nen Traum zu verwirklichen. Wir wer- Artenvielfalt birgt. Reise, und Ende Mai 2017 ging‘s los. den nicht jünger! Mir ging es nicht viel anders, als ich als Schüler Ende der 1970er Jahre in einem gigantischen 120-cm-Vollglasaquarium meine ersten „Malawis“ pflegte (heute würde man sagen: quälte) und mir mit Nachzuchten, die ich an das lokale Zoogeschäft verhökerte, Futter und Zu- behör kaufte. Es gab noch kein Internet, der Mergus-Aquarienatlas bot damals nur unzureichende Informationen über die Lebensräume und Haltungsbedin- gungen der Cichliden aus dem See, und nur gelegentlich fand man ein paar Infos in einer Aquarienzeitschrift. Auf alle Fälle nistete sich bei mir damals der Gedanke ein, irgendwann einmal Abb. 2: Blick auf Domwe, der größten Insel im Nationalpark, und Ilala Gap, den etwa 20 m breiten den See zu besuchen. -
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 ................................................. -
Rare Morph Lake Malawi Mbuna Cichlids Benefit from Reduced Aggression from Con- and Hetero-Specifics
bioRxiv preprint doi: https://doi.org/10.1101/2021.04.08.439056; this version posted April 9, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. 1 Rare morph Lake Malawi mbuna cichlids benefit from reduced aggression from con- and hetero-specifics 2 Running title: Reduced aggression benefits rare morph mbuna 3 4 Alexandra M. Tyers*, Gavan M. Cooke & George F. Turner 5 School of Biological Sciences, Bangor University, Deniol Road, Bangor. Gwynedd. Wales. UK. LL57 2UW 6 * Current address: Max Planck Institute for Biology of Ageing, Joseph-Stelzmann-Straße 9B, 50931, Köln 7 8 Corresponding author: A.M. Tyers, [email protected] 9 10 Abstract 11 Balancing selection is important for the maintenance of polymorphism as it can prevent either fixation of one 12 morph through directional selection or genetic drift, or speciation by disruptive selection. Polychromatism can 13 be maintained if the fitness of alternative morphs depends on the relative frequency in a population. In 14 aggressive species, negative frequency-dependent antagonism can prevent an increase in the frequency of rare 15 morphs as they would only benefit from increased fitness while they are rare. Heterospecific aggression is 16 common in nature and has the potential to contribute to rare morph advantage. Here we carry out field 17 observations and laboratory aggression experiments with mbuna cichlids from Lake Malawi, to investigate the 18 role of con- and heterospecific aggression in the maintenance of polychromatism and identify benefits to rare 19 mores which are likely to result from reduced aggression. -
Whose Commons? Fishermen, Developmentalists and Conservationists on Lake Malawi Anne Ferguson Department of Anthropology Michiga
WORKSHOP IN POLITICAL THEORY AND POLICY ANALYSIS 513 NORTH PARK INDIANA UNIVERSITY BLO DMINGTON, IN 47408-3895 U S > Whose Commons? Fishermen, Developmentalists and Conservationists on Lake Malawi by i Anne Ferguson Department of Anthropology Michigan State University Bill Derman Department of Anthropology . Michigan State University , Richard Mkandawire j Department of Rural Development Bunda College of Agriculture, University of Malawi September 15, 1990 Paper prepared for the First International Association for the Study of Common Property: "Designing Sustainability on the Commons", Duke University: September 3-7-30, 1990 Draft. Please do not cite without agreement of | the authors I. Introduction Fish from Lake Malawi are a major source of animal protein for large numbers of people in Malawi and Mozambique, two of Sub- Saharan Africa's poorest countries. It is estimated that fish, supplied by a dynamic and diverse small-scale African fishing industry, contribute seventy percent of animal protein consumed by Malawians per year (Alimoso et al. 1990). In this paper we briefly discuss the scale and social organization of fishing and what we have learned about use rights in the southern and central portions of Lake Malawi. We propose that the open access fishing which exists in these areas has not significantly harmed fish stocks to date, although problems may be emerging. An equal, if not greater, threatjto the fish, fishing and the ecology of Lake Malawi than that posed by open access small-scale fishing originates from developmentalists— internal and external actors advocating large-scale, capital intensive exploitation of the fish and the development of an international tourism industry. -
Distribution Extension and Ecological Aspects of One Trichomycteridae Species in a Tropical River, Amazon, Brazil
Crossref Similarity Check Powered by iThenticate SCIENTIFIC NOTE DOI: http://dx.doi.org/10.18561/2179-5746/biotaamazonia.v11n1p89-91 Distribution extension and ecological aspects of one Trichomycteridae species in a tropical river, Amazon, Brazil Lucas Pires de Oliveira1,2, Fabiano Corrêa3, Ronaldo Souza da Silva4, Vinicius Guerra1,2,5, Lisandro Juno Soares Vieira1,2 1. Laboratório de Ictiologia e Ecologia Aquática, Universidade Federal do Acre, Campus Rio Branco, Rodovia BR-364, Km 04 - Distrito Industrial, CEP 69.920-900 Rio Branco, Acre, Brazil. 2. Programa de Pós-Graduação em Ecologia e Manejo de Recursos Naturais, Universidade Federal do Acre, Campus Rio Branco, Rodovia BR 364, km 04 - Distrito Industrial, CEP 69.920-900, Rio Branco, Acre, Brazil. [email protected] http://lattes.cnpq.br/3773214446277814 http://orcid.org/0000-0003-3784-5149 [email protected] http://lattes.cnpq.br/2774068391547605 http://orcid.org/0000-0003-1912-1139 [email protected] http://lattes.cnpq.br/7161311377613700 http://orcid.org/0000-0002-2470-5684 3. Programa de Pós-Graduação em Ecologia e Conservação, Universidade do Estado do Mato Grosso, Campus Nova Xavantina, Av. Dr. Renato Figueiro Varella, Caixa Postal 08, CEP 78.690- 000, Nova Xavantina, MT, Brazil. [email protected] http://lattes.cnpq.br/9152410533692682 http://orcid.org/0000-0003-1909-5137 4. Programa de Pós-Graduação em Zoologia, Universidade Federal do Pará, Campus Básico, Rua Augusto Corrêa, 01 -Guamá, CEP 66.075-110, Belém, Pará, Brasil. [email protected] http://lattes.cnpq.br/5401270066934667 http://orcid.org/0000-0003-1909-5137 5. Instituto Boitatá de Etnobiologia e Conservação da Fauna, Goiânia, Brasil. -
Indian and Madagascan Cichlids
FAMILY Cichlidae Bonaparte, 1835 - cichlids SUBFAMILY Etroplinae Kullander, 1998 - Indian and Madagascan cichlids [=Etroplinae H] GENUS Etroplus Cuvier, in Cuvier & Valenciennes, 1830 - cichlids [=Chaetolabrus, Microgaster] Species Etroplus canarensis Day, 1877 - Canara pearlspot Species Etroplus suratensis (Bloch, 1790) - green chromide [=caris, meleagris] GENUS Paretroplus Bleeker, 1868 - cichlids [=Lamena] Species Paretroplus dambabe Sparks, 2002 - dambabe cichlid Species Paretroplus damii Bleeker, 1868 - damba Species Paretroplus gymnopreopercularis Sparks, 2008 - Sparks' cichlid Species Paretroplus kieneri Arnoult, 1960 - kotsovato Species Paretroplus lamenabe Sparks, 2008 - big red cichlid Species Paretroplus loisellei Sparks & Schelly, 2011 - Loiselle's cichlid Species Paretroplus maculatus Kiener & Mauge, 1966 - damba mipentina Species Paretroplus maromandia Sparks & Reinthal, 1999 - maromandia cichlid Species Paretroplus menarambo Allgayer, 1996 - pinstripe damba Species Paretroplus nourissati (Allgayer, 1998) - lamena Species Paretroplus petiti Pellegrin, 1929 - kotso Species Paretroplus polyactis Bleeker, 1878 - Bleeker's paretroplus Species Paretroplus tsimoly Stiassny et al., 2001 - tsimoly cichlid GENUS Pseudetroplus Bleeker, in G, 1862 - cichlids Species Pseudetroplus maculatus (Bloch, 1795) - orange chromide [=coruchi] SUBFAMILY Ptychochrominae Sparks, 2004 - Malagasy cichlids [=Ptychochrominae S2002] GENUS Katria Stiassny & Sparks, 2006 - cichlids Species Katria katria (Reinthal & Stiassny, 1997) - Katria cichlid GENUS -
Global Catfish Biodiversity 17
American Fisheries Society Symposium 77:15–37, 2011 © 2011 by the American Fisheries Society Global Catfi sh Biodiversity JONATHAN W. ARMBRUSTER* Department of Biological Sciences, Auburn University 331 Funchess, Auburn University, Alabama 36849, USA Abstract.—Catfi shes are a broadly distributed order of freshwater fi shes with 3,407 cur- rently valid species. In this paper, I review the different clades of catfi shes, all catfi sh fami- lies, and provide information on some of the more interesting aspects of catfi sh biology that express the great diversity that is present in the order. I also discuss the results of the widely successful All Catfi sh Species Inventory Project. Introduction proximately 10.8% of all fi shes and 5.5% of all ver- tebrates are catfi shes. Renowned herpetologist and ecologist Archie Carr’s But would every one be able to identify the 1941 parody of dichotomous keys, A Subjective Key loricariid catfi sh Pseudancistrus pectegenitor as a to the Fishes of Alachua County, Florida, begins catfi sh (Figure 2A)? It does not have scales, but it with “Any damn fool knows a catfi sh.” Carr is right does have bony plates. It is very fl at, and its mouth but only in part. Catfi shes (the Siluriformes) occur has long jaws but could not be called large. There is on every continent (even fossils are known from a barbel, but you might not recognize it as one as it Antarctica; Figure 1); and the order is extremely is just a small extension of the lip. There are spines well supported by numerous complex synapomor- at the front of the dorsal and pectoral fi ns, but they phies (shared, derived characteristics; Fink and are not sharp like in the typical catfi sh. -
Identification and Biology of Diplotaxodon, Rhamphochromis and Pallidochromis
190 Diplotaxodon, Rhamphochromis & Pallidochromis / Turner et al. Identification and Biology of Diplotaxodon, Rhamphochromis and Pallidochromis George F. Turner, Rosanna L. Robinson, Paul W. Shaw & Gary R. Carvalho Abstract Introduction We present preliminary morphological and mo- The genera Rhamphochromis Regan, 1922 and lecular taxonomic studies of the genera Rhampho- Diplotaxodon Trewavas, 1935 include the most chromis, Diplotaxodon and Pallidochromis, along with pelagic of Lake Malawi’s cichlids (Turner, 1996). notes on their identification, distribution and ecol- Pallidochromis Turner, 1994, a more benthic form, is ogy. We suggest that Rhamphochromis is comprised also considered in this chapter, as it appears mor- of eight to ten species: R. longiceps, R. woodi, R. phologically intermediate between Diplotaxodon macrophthalmus, R. esox, possibly R. ferox and four and Rhamphochromis (Turner 1994a). Rhampho- or five undescribed species. We suggest that R. chromis species are streamlined elongated predators lucius and R. brevis may be junior synonyms of R. of fish and zooplankton. They usually have large woodi. We also believe that Rhamphochromis teeth and jaws. Diplotaxodon comprises a heteroge- leptosoma and R. melanotus are junior synonyms of neous mix of small-toothed silvery species with R. esox. We consider that the two types of R. ferox upwardly-angled jaws. The genus includes zoo- are not conspecific and we designate a lectotype. planktivores and predators of small pelagic fish. However, we have not yet been able to positively The genus Rhamphochromis was described by identify this species from recent collections. Regan (1922), who took the type species as Diplotaxodon may contain anything from 11 to 22 or Rhamphochromis longiceps (Günther, 1864).