Microctenopoma Ansorgii - the Ornate Ctenopoma Article and Photo by ALEXANDER a PRIEST

Total Page:16

File Type:pdf, Size:1020Kb

Microctenopoma Ansorgii - the Ornate Ctenopoma Article and Photo by ALEXANDER a PRIEST FAAS Publication Awards Form Author Alexander A. Priest Society (NO Abbreviations) Greater City Aquarium Society 10 Best Spawning Article Age Category More than 1000 words (Junior Only) Date of Publication March 2013 Title of Publication (NO Abbreviations) Modern Aquarium Title of Article The Most Ornate Afrtican Replace this text with your reprint policy. Not-for-profit aquarium societies are hereby granted permission to reproduce articles and illustrations from this publication, unless the Enter your official article indicates that the copyrights have been retained by the author, and provided reprints indicate source and two copies of the publication Reprint Policy reprint policy for your are sent to the Exchange Editor of this magazine. Any other publication. reproduction or commercial use of the material in this publication is prohibited without express written prior permission. Enter email address where we should Address per your Reprint Policy above: send your digital award certificates. Stephen Sica Address Information 80-40 223 Street Award certificates should all go to the same address. Hollis Hills, NY 11427 [email protected] OK to type in your Signature Dan Radebaugh DHR signature & initials. By submitting this entry, I attest that the publication pages have not been materially altered from my society’s originally published document. Form Directions For Junior Entries, e.g Junior Level 1: 1) Fill out the form above. J1-013-002.pdf 2) Convert or “print” to PDF 3) Combine form with the PDF version of the article being submitted. 4) Name file as follows e.g. Greater Colorado Corydoras Association Category 13 Entry #2 013-002-gcca.pdf Microctenopoma ansorgii - The Ornate Ctenopoma Article and photo by ALEXANDER A PRIEST nabantoids are fish in the suborder Ctenopoma are basically egg scatterers. Their eggs Anabantoidei. They possess a labyrinth generally float to the surface, and usually remain A(or, “maze-like”) organ consisting of together under surface debris. Although this multiple folded compartments of thin boney plates floating mass of eggs can resemble a “nest,” it was in the head. Those boney plates, called lamellae, neither intentionally constructed nor will it are covered with thin membranes that allow subsequently be tended or defended. oxygen in the air to pass directly into the fish’s The subject of this article, Microctenopoma blood stream, giving these fish the ability to ansorgii, is probably the most recognizable and survive in stagnant, oxygen-poor water that would “colorful” (if black and orange means that to you) not be able to sustain fish having to rely on gills of the Ctenopoma and Microctenopoma group. In alone to filter oxygen dissolved in the water. (The fact, its generally accepted common names are word “anabantoid” comes from a Greek word “Ornate Ctenopoma” (going back to when this meaning to “travel up,” referring to these fish species was in the genus Ctenopoma) and “Ornate going up to the water’s surface to gulp air.) Bushfish” (they can survive for extended periods The most in mud and wet leaf commonly kept Scientific Name: Microctenopoma ansorgii litter, so live anabantoids in the Common Names: Ornate Ctenopoma, specimens can home aquarium are Ornate Bushfish, Orange Ctenopoma sometimes be found all endemic to Asia Temperature: 70-82°F (21-28°C) “in the bush” on (betta and gourami pH Range: 6.0-8.0 (acidic: 6.5 to 6.7 optimal) land near water). species). African Hardness: 5-20°DH (soft) Another anabantoids are not Size: Up to 2.5 inches (6.4cm) SL common name often as popular or well Temperament: Males can be aggressive to each associated with known among other; smaller fish may be eaten Microctenopoma aquarium hobbyists Native habitat: Congo River basin ansorgii is “Orange for several reasons, Aquascaping: Heavily planted tank and/or tank Ctenopoma,” so including the fact with multiple caves and roots, tight lid, named for the that African dim lighting vertical orange anabantoids are Nutrition: Carnivorous, requiring live food (often more reddish) generally less (or moving frozen or gel) stripes on a dark colorful, not easy to brown body that are acclimatize, and distinctive of this tend to be shy and species. The rays on reclusive. They also require live food, and are the dorsal and anal fins come to sharp points, difficult to nearly impossible to breed in captivity. resembling a saw or “comb.” (The word There are currently three recognized genera Ctenopoma comes from two Greek words: kteis, or of African anabantoids: Ctenopoma, ktenos, meaning comb and poma, meaning Microctenopoma, and Sandelia. A review of the “cover.”) The species name ansorgii (sometimes popular Internet website Fishbase.org shows at found in older literature as ansorgei) comes from least 40 currently recognized species of the zoologist William John Ansorge (1850-1913), Ctenopoma and 12 species of Microctenopoma.1 who first discovered them. (The genus Microctenopoma is relatively new. It Microctenopoma ansorgii are native to the was first described in 1995 by the ichthyologist Congo River basin in parts of both the Republic of Steven M. Norris, who placed some species from Congo and Democratic Republic of Congo. A the genus Ctenopoma into a new genus, feral population may also exist on the island of Microctenopoma.)2 Madagascar.3 Microctenopoma are defined by several bone This is not a large fish, usually attaining a differences from Ctenopoma, not because the fish maximum adult standard length (nose to start of are smaller in size. In addition, Microctenopoma caudal, or tail fin) of about 2.5 inches (6.4 exhibit noticeable sexual dimorphism, and centimeters) and a total length (tip of nose to end behavioral characteristics that include bubble-nest of caudal) of about 3 inches (7.6 cm). Males are building and defense. Species in the genus somewhat larger, with larger dorsal and anal fins 26 Modern Aquarium - Greater City A.S. (NY) MarchMarch 2013 2013 Modern Aquarium - Greater City A.S17 (NY) having white on the distal edge. One pair can be a long while (unless they were sick or very old to kept in a 5.5 gallon (or 20 liter) tank. Two pair can start with). Frequent but small water changes are be housed in a tank twice that size, but it must be much better than large changes, unless you are heavily planted and have numerous caves, roots, able to match nearly perfectly the chemistry of the and other hiding places, providing limited “line of water removed. (Even changes for the better sight,” as males can become very territorial and should be gradual, except in an emergency such as will fight if they can see each other. This is not a a total tank breakdown.) schooling or very active fish. Mostly, they stay out Microctenopoma ansorgii are bubblenesters. of sight of each The male builds a other (and, nest of bubbles unfortunately, also under a floating out of sight of the leaf or other aquarist), each in floating material. his or her own cave For this reason, or tangle of roots filtration should or driftwood. The provide minimal tank sizes I surface water provided above are movement. Sponge absolute filters are my first minimums—larger choice, and they is better, and also provide a free recommended. source of infusoria Members of for newly hatched the Ctenopoma and fry. Microctenopoma Microctenopoma ansorgii Spawning genera are occurs under the “ambush predators,” meaning that they will wait in nest, with the male wrapping himself around the hiding for their food, seize it, then return to their female to expel eggs. The eggs (reported to be as hiding places (“ambushing” the food). They are many as 600 in a single spawning, but in my primarily carnivores. I feed mine live blackworms experience closer to 100) hatch in around 24 hours. and live brine shrimp (the latter I pre-treat with The fry should not be fed until they are liquid freshwater fish vitamins, because adult brine free-swimming, usually within two to three days. shrimp are relatively low in nutrition). I have They can then be fed very small foods such as found that they just ignore dry flake or pellet green water, paramecia, infusoria, or artificial foods, but they will eat frozen or gel food as long plankton rotifer (APR). It is advisable to remove as it is moving (meaning, I stir up the water when the parents after hatching. After about one week, I feed anything that doesn’t move by itself). slightly larger sized food can be given to the fry, Even though they are native to Africa, their such as brine shrimp nauplii and microworms. care and maintenance is very similar to that These are pretty fish, when you can see them, required for Asian anabantoids. They prefer soft, especially a male in full display. Unfortunately, slightly acidic water. Their tank should have most of the time they are in hiding and even when subdued lighting. Because they are powerful (and they dart out to grab some food, they rarely look as sudden) jumpers, the tank should be tightly good as some of those photos in the books or covered. magazines. This is also not a beginner’s fish, nor Once established in an aquarium, is it one to get with the intention of having it Microctenopoma ansorgii are surprisingly hardy spawn. (They will spawn in the home aquarium, for a small fish. The problem is that they do not but this is fairly rare.) acclimatize well at the beginning. But, if you Nonetheless, they are interesting and every provide the proper water parameters and tank now and then, if you keep them in ideal conditions, conditions, whatever fish you still have after their you will be rewarded with a sight that makes it first three weeks in your tank will probably live for very clear why they are called “ornate.” 1 http://www.fishbase.org 2 Norris, Steven M.: Microctenopoma uelense and M.
Recommended publications
  • 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 .................................................
    [Show full text]
  • Wainwright-Et-Al.-2012.Pdf
    Copyedited by: ES MANUSCRIPT CATEGORY: Article Syst. Biol. 61(6):1001–1027, 2012 © The Author(s) 2012. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For Permissions, please email: [email protected] DOI:10.1093/sysbio/sys060 Advance Access publication on June 27, 2012 The Evolution of Pharyngognathy: A Phylogenetic and Functional Appraisal of the Pharyngeal Jaw Key Innovation in Labroid Fishes and Beyond ,∗ PETER C. WAINWRIGHT1 ,W.LEO SMITH2,SAMANTHA A. PRICE1,KEVIN L. TANG3,JOHN S. SPARKS4,LARA A. FERRY5, , KRISTEN L. KUHN6 7,RON I. EYTAN6, AND THOMAS J. NEAR6 1Department of Evolution and Ecology, University of California, One Shields Avenue, Davis, CA 95616; 2Department of Zoology, Field Museum of Natural History, 1400 South Lake Shore Drive, Chicago, IL 60605; 3Department of Biology, University of Michigan-Flint, Flint, MI 48502; 4Department of Ichthyology, American Museum of Natural History, Central Park West at 79th Street, New York, NY 10024; 5Division of Mathematical and Natural Sciences, Arizona State University, Phoenix, AZ 85069; 6Department of Ecology and Evolution, Peabody Museum of Natural History, Yale University, New Haven, CT 06520; and 7USDA-ARS, Beneficial Insects Introduction Research Unit, 501 South Chapel Street, Newark, DE 19713, USA; ∗ Correspondence to be sent to: Department of Evolution & Ecology, University of California, One Shields Avenue, Davis, CA 95616, USA; E-mail: [email protected]. Received 22 September 2011; reviews returned 30 November 2011; accepted 22 June 2012 Associate Editor: Luke Harmon Abstract.—The perciform group Labroidei includes approximately 2600 species and comprises some of the most diverse and successful lineages of teleost fishes.
    [Show full text]
  • A Fossil Climbing Perch from the Oligocene of Tibet Helps Solve The
    Science Bulletin 64 (2019) 455–463 Contents lists available at ScienceDirect Science Bulletin journal homepage: www.elsevier.com/locate/scib Article Into Africa via docked India: a fossil climbing perch from the Oligocene of Tibet helps solve the anabantid biogeographical puzzle ⇑ ⇑ Feixiang Wu a,b, , Dekui He c, , Gengyu Fang d, Tao Deng a,b,d a Key Laboratory of Vertebrate Evolution and Human Origins, Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences, Beijing 100044, China b Center for Excellence in Life and Paleoenvironment, Chinese Academy of Sciences, Beijing 100101, China c Key Laboratory of Aquatic Biodiversity and Conservation, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China d College of Earth Sciences, University of Chinese Academy of Sciences, Beijing 100049, China article info abstract Article history: The northward drift of the Indian Plate and its collision with Eurasia have profoundly impacted the evo- Received 7 March 2019 lutionary history of the terrestrial organisms, especially the ones along the Indian Ocean rim. Climbing Received in revised form 22 March 2019 perches (Anabantidae) are primary freshwater fishes showing a disjunct south Asian-African distribution, Accepted 22 March 2019 but with an elusive paleobiogeographic history due to the lack of fossil evidence. Here, based on an Available online 28 March 2019 updated time-calibrated anabantiform phylogeny integrating a number of relevant fossils, the divergence between Asian and African climbing perches is estimated to have occurred in the middle Eocene (ca. Keywords: 40 Ma, Ma: million years ago), a time when India had already joined with Eurasia. The key fossil lineage Climbing perches is yEoanabas, the oldest anabantid known so far, from the upper Oligocene of the Tibetan Plateau.
    [Show full text]
  • Out of Lake Tanganyika: Endemic Lake Fishes Inhabit Rapids of the Lukuga River
    355 Ichthyol. Explor. Freshwaters, Vol. 22, No. 4, pp. 355-376, 5 figs., 3 tabs., December 2011 © 2011 by Verlag Dr. Friedrich Pfeil, München, Germany – ISSN 0936-9902 Out of Lake Tanganyika: endemic lake fishes inhabit rapids of the Lukuga River Sven O. Kullander* and Tyson R. Roberts** The Lukuga River is a large permanent river intermittently serving as the only effluent of Lake Tanganyika. For at least the first one hundred km its water is almost pure lake water. Seventy-seven species of fish were collected from six localities along the Lukuga River. Species of cichlids, cyprinids, and clupeids otherwise known only from Lake Tanganyika were identified from rapids in the Lukuga River at Niemba, 100 km from the lake, whereas downstream localities represent a Congo River fish fauna. Cichlid species from Niemba include special- ized algal browsers that also occur in the lake (Simochromis babaulti, S. diagramma) and one invertebrate picker representing a new species of a genus (Tanganicodus) otherwise only known from the lake. Other fish species from Niemba include an abundant species of clupeid, Stolothrissa tanganicae, otherwise only known from Lake Tangan- yika that has a pelagic mode of life in the lake. These species demonstrate that their adaptations are not neces- sarily dependent upon the lake habitat. Other endemic taxa occurring at Niemba are known to frequent vegetat- ed shore habitats or river mouths similar to the conditions at the entrance of the Lukuga, viz. Chelaethiops minutus (Cyprinidae), Lates mariae (Latidae), Mastacembelus cunningtoni (Mastacembelidae), Astatotilapia burtoni, Ctenochromis horei, Telmatochromis dhonti, and Tylochromis polylepis (Cichlidae). The Lukuga frequently did not serve as an ef- fluent due to weed masses and sand bars building up at the exit, and low water levels of Lake Tanganyika.
    [Show full text]
  • Supporting Information
    Supporting Information Near et al. 10.1073/pnas.1304661110 SI Text and SD of 0.8 to set 57.0 Ma as the minimal age offset and 65.3 Ma as the 95% soft upper bound. Fossil Calibration Age Priors † Here we provide, for each fossil calibration prior, the identity of Calibration 7. Trichophanes foliarum, calibration 13 in Near et al. the calibrated node in the teleost phylogeny, the taxa that rep- (1). Prior setting: a lognormal prior with the mean of 1.899 and resent the first occurrence of the lineage in the fossil record, SD of 0.8 to set 34.1 Ma as the minimal age offset and 59.0 Ma as a description of the character states that justify the phylogenetic the 95% soft upper bound. placement of the fossil taxon, information on the stratigraphy of Calibration 8. †Turkmene finitimus, calibration 16 in Near et al. the rock formations bearing the fossil, and the absolute age es- (1). Prior setting: a lognormal prior with the mean of 2.006 and timate for the fossil; outline the prior age setting used in the SD of 0.8 to set 55.8 Ma as the minimal age offset and 83.5 Ma as BEAST relaxed clock analysis; and provide any additional notes the 95% soft upper bound. on the calibration. Less detailed information is provided for 26 of the calibrations used in a previous study of actinopterygian di- Calibration 9. †Cretazeus rinaldii, calibration 14 in Near et al. (1). vergence times, as all the information and prior settings for these Prior setting: a lognormal prior with the mean of 1.016 and SD of calibrations is found in the work of Near et al.
    [Show full text]
  • Was Bedeutet „Labyrinthfische“? 10 Systematik Und Morphologie 12 Das Wasser Und Seine Werte 14 Das Aquarium Für Labyrinthfi
    Was bedeutet „Labyrinthfische“? 10 Betta hipposideros 78 Systematik und Morphologie 12Betta ibanorum 79 Das Wasser und seine Werte 14 Betta ideii 80 Das Aquarium für Labyrinthfische 16Betta imbellis 82 Futter für Labyrinthfische 18 Betta krataios 86 Betta kuehnei 88 Labyrinthfische aus Asien 20 Betta lehi 90 Betta livida 91 Die GattungAnabas 22 Betta macrostoma 92 Anabas cobojius 23 Betta mahachaiensis 96 Anabas testudineus 24 Betta mandor 98 Betta midas 99 Die GattungBelontia 26 Betta miniopinna 100 Belontia hasselti 21 Betta obscura 101 Belontia signata 29 Betta ocellata 102 Betta pallida 103 Die GattungBetta 31 Betta pallifina 104 Verwandschaftsstruktur Bettader -Arten 32 Betta pardalotus 105 FortpflanzungssmerkmaleBetta-G der ruppen 35 Betta patoti 106 Betta persephone 107 Betta akarensis 38 Betta pi 108 Betta albimarginata 39 Betta picta 110 Betta anabatoides 41 Betta pinguis 113 Betta antoni 42 Betta prima 114 Betta apollon 43 Betta pugnax 115 Betta aurigans 45 Betta pulchra 117 Betta balunga 47 Betta raja 118 Betta bellica 48 Betta renata 119 Betta breviobesus 49 Betta rubra 120 Betta brownorum 50 Betta rutilans 122 Betta burdigala 52 Betta schallen 123 Betta channoides 55 Betta siamorientalis 124 Betta chini 57 Betta simorum 126 Betta chloropharynx 58 Betta simplex 127 Betta cocäna 59 Betta smaragdina 129 Betta compuncta 61 Betta sp. Airplaik 132 Betta cracens 62 Betta sp. Bukit Lawang 133 Betta dennisyongi 64 Betta sp. Danau Calak 134 Betta dimidiata 66 Betta sp. Duc Hua 135 Betta edithae 67 Betta sp. Jantur Gemuruh 136 Betta enisae 68 Betta sp. Kubu 137 Bettafalx 69 Betta sp. Lake Luar 138 Bettaferox 71 Betta sp.
    [Show full text]
  • UNIVERSITY of CALIFORNIA SANTA CRUZ Biodiversity, Biogeography
    UNIVERSITY OF CALIFORNIA SANTA CRUZ Biodiversity, Biogeography, and Conservation of Freshwater Fishes in Gabon A dissertation submitted in partial satisfaction of the requirements for the degree of DOCTOR OF PHILOSOPHY in ECOLOGY AND EVOLUTIONARY BIOLOGY By Joseph S. Cutler September 2019 The Dissertation of Joseph S. Cutler is approved: ______________________________ Dr. Don Croll, Chair ______________________________ Dr. Giacomo Bernardi ______________________________ Dr. Eric Palkovacs ______________________________ Dr. Brian Sidlauskas ______________________________ Dr. Bernie Tershy ______________________________ Quentin Williams Acting Vice Provost and Dean of Graduate Studies Table of Contents List of Figures iv Abstract vi Acknowledgements vii Introduction 1 Chapter 1 6 Chapter 2 49 Chapter 3 130 Chapter 4 147 Conclusion 162 Bibliography 166 iii List of Figures Chapter 1 1.1. Figure 1.1…………………………………………………………………... 11 1.2. Figure 1.2…………………………………………………………………... 12 1.3. Figure 1.3……………………………………………………………………15 1.4. Figure 1.4……………………………………………………………........... 16 1.5. Figure 1.5…………………………………………………………………... 16 1.6. Figure 1.6…………………………………………………………………... 20 1.7. Figure 1.7…………………………………………………………………... 21 1.8. Figure 1.8…………………………………………………………………... 23 1.9. Figure 1.9…………………………………………………………………... 25 1.10. Figure 1.10…………………………………………………………………. 27 1.11. Figure 1.11…………………………………………………………………. 32 1.12. Figure 1.12…………………………………………………………………. 34 1.13. Figure 1.13…………………………………………………………………. 36 1.14. Figure 1.14…………………………………………………………………. 40 Chapter 2 2.1. Figure 2.1…………………………………………………………………... 52 2.2. Figure 2.2…………………………………………………………………... 55 2.3. Figure 2.3……………………………………………………………………57 2.4. Table 2.2……………………………………………………………..……...58 iv 2.5. Figure 2.4……………………………………………………………………63 2.6. Figure 2.5……………………………………………………………………71 2.7. Figure 2.6……………………………………………………………………79 2.8. Figure 2.7……………………………………………………………………83 2.9. Figure 2.8……………………………………………………………………92 2.10. Figure 2.9……………………………………………………………………94 2.11.
    [Show full text]
  • Where Ichthyofaunal Provinces Meet: the Fish Fauna of the Lake Edward System
    ACCEPTED MANUSCRIPT, UNCORRECTED, NOT TO BE USED FOR CITATIONS, REFERENCING OR TAXONOMIC PURPOSES 1 Where ichthyofaunal provinces meet: the fish fauna of the Lake Edward system 2 3 E. Decru1,2†, N. Vranken1,2, P. H. N. Bragança3, J. Snoeks1,2 & M. Van Steenberge1,2,4 4 5 1Section Vertebrates, Biology Department, Royal Museum for Central Africa, 6 Leuvensesteenweg 13, 3080, Tervuren, Belgium 7 2Laboratory of Biodiversity and Evolutionary Genomics, Department of Biology, University 8 of Leuven, Ch. Deberiotstraat 32, B-3000 Leuven, Belgium 9 3Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro, 10 Av. Pedro Calmon, 550, Rio de Janeiro, RJ, 21941-901, Brazil 11 4Operational Directorate Taxonomy and Phylogeny, Royal Belgian Institute of Natural 12 Sciences, Vautier Street, 29, 1000 Brussels 13 14 †Author to whom correspondence should be addressed. Tel.: +32(0)2 769 56 32; email: 15 [email protected] 16 1 16 17 ABSTRACT 18 Based on literature, museum collections and three recent expeditions, an annotated species list 19 of the Lake Edward drainage system is presented, excluding the endemic haplochromines. A 20 total of 34 non-Haplochromis species belonging to 10 families and 21 genera are recorded 21 from the system. Three of these are endemic and two others have been introduced in the 22 region. Six species are new records for the Lake Edward system. A species accumulation 23 curve indicates that we probably covered most of the non-Haplochromis species in the area 24 sampled during the recent expeditions. However, undetected species might still be present in 25 the Congolese part of the system, which is poorly sampled.
    [Show full text]
  • A Strategic Approach to the Management of Ornamental Fish in Australia Communication Strategy and Grey List Review - a REPORT to OFMIG
    A strAtegic ApproAch to the management of ornamental fish in australia communicAtion strAtegy And grey list review - A report TO oFmig A strategic approach to the management of ornamental fish in Australia Communication strategy and grey list review – a report to OFMIG Andy Moore, Nicholas Marton and Alex McNee March 2010 © Commonwealth of Australia 2010 This work is copyright. Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from the Commonwealth. Requests and inquiries concerning reproduction and rights should be addressed to the Commonwealth Copyright Administration, Attorney General’s Department, Robert Garran Offices, National Circuit, Barton ACT 2600 or posted at http://www.ag.gov.au/cca. The Australian Government acting through the Bureau of Rural Sciences has exercised due care and skill in the preparation and compilation of the information and data set out in this publication. Notwithstanding, the Bureau of Rural Sciences, its employees and advisers disclaim all liability, including liability for negligence, for any loss, damage, injury, expense or cost incurred by any person as a result of accessing, using or relying upon any of the information or data set out in this publication to the maximum extent permitted by law. Postal address: Bureau of Rural Sciences GPO Box 858 Canberra, ACT 2601 Copies available from: www.brs.gov.au ISBN: 1-921192-37-2 ii Acknowledgements This report was made possible through financial support from the Ornamental Fish Management Implementation Group (OFMIG) which is funded by state, teritory and federal government agencies.
    [Show full text]
  • Fish Biodiversity Assessment of the Rapids of Mboungou Badouma and Doumé Ramsar Site and Surrounding Areas in Gabon
    Fish Biodiversity Assessment of the Rapids of Mboungou Badouma and Doumé Ramsar Site and Surrounding Areas in Gabon Joseph Cutler, Colin Apse, Thibault Cavelier de Cuverville, Yves Fermon, Jean-Hervé Mvé-Beh, Marie-Claire Paiz, Brian Sidlauskas, John P. Sullivan Suggested Citation Cutler J., Apse C., Cavelier T., Fermon, Y., Mvé-Beh, J-H., Paiz, M-C., Sidlauskas, B., and Sullivan, J.P. 2015. Fish Biodiversity Assessment of the Rapids of Mboungou Badouma and Doumé Ramsar Site and Surrounding Areas in Gabon. The Nature Conservancy, Arlington, VA. Table of Contents Acknowledgments ii Executive Summary ii Introduction 1 About this Report 1 Expedition Team 2 Geographic Context 2 The Human Context 4 Socio-Economic Uses and Threats 4 History of Ichthyological Exploration 5 Field and Identification Methods 9 Results from Field Sampling 12 Sampling Sites 12 Taxon-Based Results 14 Osteoglossiformes 14 Characiformes 19 Cyprinodontiformes 23 Cypriniformes 25 Perciformes 29 Siluriformes 31 Synbranchiformes 36 Clupeiformes 37 Fishing-Gear Based Results 37 Results from Data Analysis 40 Species Distribution Analysis 40 Relationship between Substrate and Species 41 Notable Fishes and Problematic Identifications 42 Notes on Use of Social Media 44 Conclusion and Initial Recommendations 45 Reference Literature 47 Appendix 1. Sampling at Doumé: Comparing Modern and Historic Collections 51 Appendix 2. List of Species Known and Collected from the Ogooué River and its Major Tributaries around the Ramsar Site 55 Appendix 3. Ecology and Status of the Fishes from the Ogooué River Basin 62 Appendix 4. All Sampling Sites 69 Acknowledgments The authors of this report would like to express their gratitude to the community leaders, local authorities and citizens of the villages and towns visited during this expedition for their welcome and tremendous support and assistance in facilitating both the successful sampling and the well-being of the researchers.
    [Show full text]
  • 30. Anabantidae = 30. Anabantidae
    30. ANABANTIDAE Steven Mark NORRIS African Anabantidae are elongate or deep-bodied, fully scaled, with large eyes, a terminal mouth and unspecialized, conical teeth. They, like cichlids, are easily recognised by an interrupted lateral line, with an upper and lower branch. All have the first epibranchial gill arch elements greatly expanded and forming suprabranchial, accessory breathing organs (= labyrinth organs). In most species, some or all of the opercular bones have serrate, distal margins. Anabantidae are widely distributed in South-east Asia and Africa and most authors recognise two African genera; Ctenopoma encompassed all tropical forms, and two temperate species from extreme South Africa placed in Sandelia. However, Ctenopoma so constructed is polyphyletic and NORRIS (1994, 1995) restricted the genus Ctenopoma to just three species, transferring most species to either Microctenopoma or to a yet unnamed genus herein referred to as “Ctenopoma”. Anabantids are commonly found in oxygen-deficient waters, such as marshes, inundated forests or grasslands and river margins. Life history data on African species are few and largely anecdotal; most species appear to feed primarily on aquatic and terrestrial invertebrates. Two genera (Microctenopoma and Sandelia) show specialized breeding strategies with nest-building and parental care. Currently there are approximately 25 African species recognised, of which eight are represented in Lower Guinea. KEY 1 16 segmented caudal rays. Body deep, contained 2-3 times in TO GENERA SL. Swim bladder with paired anterior extensions. Males with postocular, ocular and caudal peduncle contact organs (fig. 30.1) ......................................................................... “Ctenopoma” 14 segmented caudal rays. Body elongate, contained three or more times in SL.
    [Show full text]
  • Unrestricted Species
    UNRESTRICTED SPECIES Actinopterygii (Ray-finned Fishes) Atheriniformes (Silversides) Scientific Name Common Name Bedotia geayi Madagascar Rainbowfish Melanotaenia boesemani Boeseman's Rainbowfish Melanotaenia maylandi Maryland's Rainbowfish Melanotaenia splendida Eastern Rainbow Fish Beloniformes (Needlefishes) Scientific Name Common Name Dermogenys pusilla Wrestling Halfbeak Characiformes (Piranhas, Leporins, Piranhas) Scientific Name Common Name Abramites hypselonotus Highbacked Headstander Acestrorhynchus falcatus Red Tail Freshwater Barracuda Acestrorhynchus falcirostris Yellow Tail Freshwater Barracuda Anostomus anostomus Striped Headstander Anostomus spiloclistron False Three Spotted Anostomus Anostomus ternetzi Ternetz's Anostomus Anostomus varius Checkerboard Anostomus Astyanax mexicanus Blind Cave Tetra Boulengerella maculata Spotted Pike Characin Carnegiella strigata Marbled Hatchetfish Chalceus macrolepidotus Pink-Tailed Chalceus Charax condei Small-scaled Glass Tetra Charax gibbosus Glass Headstander Chilodus punctatus Spotted Headstander Distichodus notospilus Red-finned Distichodus Distichodus sexfasciatus Six-banded Distichodus Exodon paradoxus Bucktoothed Tetra Gasteropelecus sternicla Common Hatchetfish Gymnocorymbus ternetzi Black Skirt Tetra Hasemania nana Silver-tipped Tetra Hemigrammus erythrozonus Glowlight Tetra Hemigrammus ocellifer Head and Tail Light Tetra Hemigrammus pulcher Pretty Tetra Hemigrammus rhodostomus Rummy Nose Tetra *Except if listed on: IUCN Red List (Endangered, Critically Endangered, or Extinct
    [Show full text]