Trends in Freshwater Microcrustaceans Studies in Brazil Between 1990 and 2014 W
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Cladocera: Anomopoda: Daphniidae) from the Lower Cretaceous of Australia
Palaeontologia Electronica palaeo-electronica.org Ephippia belonging to Ceriodaphnia Dana, 1853 (Cladocera: Anomopoda: Daphniidae) from the Lower Cretaceous of Australia Thomas A. Hegna and Alexey A. Kotov ABSTRACT The first fossil ephippia (cladoceran exuvia containing resting eggs) belonging to the extant genus Ceriodaphnia (Anomopoda: Daphniidae) are reported from the Lower Cretaceous (Aptian) freshwater Koonwarra Fossil Bed (Strzelecki Group), South Gippsland, Victoria, Australia. They represent only the second record of (pre-Quater- nary) fossil cladoceran ephippia from Australia (Ceriodaphnia and Simocephalus, both being from Koonwarra). The occurrence of both of these genera is roughly coincident with the first occurrence of these genera elsewhere (i.e., Mongolia). This suggests that the early radiation of daphniid anomopods predates the breakup of Pangaea. In addi- tion, some putative cladoceran body fossils from the same locality are reviewed; though they are consistent with the size and shape of cladocerans, they possess no cladoceran-specific synapomorphies. They are thus regarded as indeterminate diplostracans. Thomas A. Hegna. Department of Geology, Western Illinois University, Macomb, IL 61455, USA. ta- [email protected] Alexey A. Kotov. A.N. Severtsov Institute of Ecology and Evolution, Leninsky Prospect 33, Moscow 119071, Russia and Kazan Federal University, Kremlevskaya Str.18, Kazan 420000, Russia. alexey-a- [email protected] Keywords: Crustacea; Branchiopoda; Cladocera; Anomopoda; Daphniidae; Cretaceous. Submission: 28 March 2016 Acceptance: 22 September 2016 INTRODUCTION tions that the sparse known fossil record does not correlate with a meager past diversity. The rarity of Water fleas (Crustacea: Cladocera) are small, the cladoceran fossils is probably an artifact, a soft-bodied branchiopod crustaceans and are a result of insufficient efforts to find them in known diverse and ubiquitous component of inland and new palaeontological collections (Kotov, aquatic communities (Dumont and Negrea, 2002). -
Aquatic Invertebrates and Waterbirds of Wetlands and Rivers of the Southern Carnarvon Basin, Western Australia
DOI: 10.18195/issn.0313-122x.61.2000.217-265 Records of the Western Australian Museum Supplement No. 61: 217-265 (2000). Aquatic invertebrates and waterbirds of wetlands and rivers of the southern Carnarvon Basin, Western Australia 3 3 S.A. Halsel, R.J. ShieF, A.W. Storey, D.H.D. Edward , I. Lansburyt, D.J. Cale and M.S. HarveyS 1 Department of Conservation and Land Management, Wildlife Research Centre, PO Box 51, Wanneroo, Western Australia 6946, Australia 2CRC for Freshwater Ecology, Murray-Darling Freshwater Research Centre, PO Box 921, Albury, New South Wales 2640, Australia 3 Department of Zoology, The University of Western Australia, Nedlands, Western Australia 6907, Australia 4 Hope Entomological Collections, Oxford University Museum, Parks Road, Oxford OXl 3PW, United Kingdom 5 Department of Terrestrial Invertebrates, Western Australian Museum, Francis Street, Perth, Western Australia 6000, Australia Abstract - Fifty-six sites, representing 53 wetlands, were surveyed in the southern Carnarvon Basin in 1994 and 1995 with the aim of documenting the waterbird and aquatic invertebrate fauna of the region. Most sites were surveyed in both winter and summer, although some contained water only one occasion. Altogether 57 waterbird species were recorded, with 29 292 waterbirds of 25 species on Lake MacLeod in October 1994. River pools were shown to be relatively important for waterbirds, while many freshwater claypans were little used. At least 492 species of aquatic invertebrate were collected. The invertebrate fauna was characterized by the low frequency with which taxa occurred: a third of the species were collected at a single site on only one occasion. -
Freshwater Crustaceans As an Aboriginal Food Resource in the Northern Great Basin
UC Merced Journal of California and Great Basin Anthropology Title Freshwater Crustaceans as an Aboriginal Food Resource in the Northern Great Basin Permalink https://escholarship.org/uc/item/3w8765rq Journal Journal of California and Great Basin Anthropology, 20(1) ISSN 0191-3557 Authors Henrikson, Lael S Yohe, Robert M, II Newman, Margaret E et al. Publication Date 1998-07-01 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Joumal of Califomia and Great Basin Anthropology Vol. 20, No. 1, pp. 72-87 (1998). Freshwater Crustaceans as an Aboriginal Food Resource in the Northern Great Basin LAEL SUZANN HENRIKSON, Bureau of Land Management, Shoshone District, 400 W. F Street, Shoshone, ID 83352. ROBERT M. YOHE II, Archaeological Survey of Idaho, Idaho State Historical Society, 210 Main Street, Boise, ID 83702. MARGARET E. NEWMAN, Dept. of Archaeology, University of Calgary, Alberta, Canada T2N 1N4. MARK DRUSS, Idaho Power Company, 1409 West Main Street, P.O. Box 70. Boise, ID 83707. Phyllopods of the genera Triops, Lepidums, and Branchinecta are common inhabitants of many ephemeral lakes in the American West. Tadpole shrimp (Triops spp. and Lepidums spp.) are known to have been a food source in Mexico, and fairy shrimp fBranchinecta spp.) were eaten by the aborigi nal occupants of the Great Basin. Where found, these crustaceans generally occur in numbers large enough to supply abundant calories and nutrients to humans. Several ephemeral lakes studied in the Mojave Desert arul northern Great Basin currently sustain large seasonal populations of these crusta ceans and also are surrounded by numerous small prehistoric camp sites that typically contain small artifactual assemblages consisting largely of milling implements. -
Table of Contents 2
Southwest Association of Freshwater Invertebrate Taxonomists (SAFIT) List of Freshwater Macroinvertebrate Taxa from California and Adjacent States including Standard Taxonomic Effort Levels 1 March 2011 Austin Brady Richards and D. Christopher Rogers Table of Contents 2 1.0 Introduction 4 1.1 Acknowledgments 5 2.0 Standard Taxonomic Effort 5 2.1 Rules for Developing a Standard Taxonomic Effort Document 5 2.2 Changes from the Previous Version 6 2.3 The SAFIT Standard Taxonomic List 6 3.0 Methods and Materials 7 3.1 Habitat information 7 3.2 Geographic Scope 7 3.3 Abbreviations used in the STE List 8 3.4 Life Stage Terminology 8 4.0 Rare, Threatened and Endangered Species 8 5.0 Literature Cited 9 Appendix I. The SAFIT Standard Taxonomic Effort List 10 Phylum Silicea 11 Phylum Cnidaria 12 Phylum Platyhelminthes 14 Phylum Nemertea 15 Phylum Nemata 16 Phylum Nematomorpha 17 Phylum Entoprocta 18 Phylum Ectoprocta 19 Phylum Mollusca 20 Phylum Annelida 32 Class Hirudinea Class Branchiobdella Class Polychaeta Class Oligochaeta Phylum Arthropoda Subphylum Chelicerata, Subclass Acari 35 Subphylum Crustacea 47 Subphylum Hexapoda Class Collembola 69 Class Insecta Order Ephemeroptera 71 Order Odonata 95 Order Plecoptera 112 Order Hemiptera 126 Order Megaloptera 139 Order Neuroptera 141 Order Trichoptera 143 Order Lepidoptera 165 2 Order Coleoptera 167 Order Diptera 219 3 1.0 Introduction The Southwest Association of Freshwater Invertebrate Taxonomists (SAFIT) is charged through its charter to develop standardized levels for the taxonomic identification of aquatic macroinvertebrates in support of bioassessment. This document defines the standard levels of taxonomic effort (STE) for bioassessment data compatible with the Surface Water Ambient Monitoring Program (SWAMP) bioassessment protocols (Ode, 2007) or similar procedures. -
Check List the Journal Of
13 3 the journal of 2144 biodiversity data 17 June 2017 Check List NOTES ON GEOGRAPHIC DISTRIBUTION Check List 13(3): 2144, 17 June 2017 https://doi.org/10.15560/13.3.2144 ISSN 1809-127X © 2017 Check List and Authors First record of Moina dumonti Kotov, Elías-Gutiérrez & Granado- Ramírez, 2005 (Branchiopoda: Anomopoda) in Brazil Daniel da Silva Farias,1, 3 Lourdes Maria Abdu Elmoor-Loureiro2 & Christina Wyss Castelo Branco1 1 Núcleo de Estudos Limnológicos, Universidade Federal do Estado do Rio de Janeiro, Av. Pasteur, 458, IBIO, sala 403, CEP 22290-240, Rio de Janeiro, RJ, Brazil 2 Laboratório de Zoologia, Universidade Católica de Brasília, QS 7 lote 1, Bloco M, sala 331, CEP 71966-700, Taguatinga, DF, Brazil 3 Corresponding author. E-mail: [email protected] Abstract. The cladoceran Moina dumonti Kotov, Elías- of the water surface and has also Lemna minor L. in marginal Gutiérrez & Granado-Ramírez, 2005 (Anomopoda: Moinidae) areas. This waterbody is part of the lagoon system of Jacarep- was found in a hypereutrophic lagoon, Lagoinha, Rio de aguá, which also includes the lagoons of Jacarepaguá, Camor- Janeiro, Brazil. It represents the first record of this species in im, Tijuca and Marapendi (Soares 1999). The lagoon system is Brazil and in the Southern Hemisphere; it also represents the polluted by the inflow of rainwater drainage, untreated sewage, first record of this species in a perennial lagoon. The reasons and wastes from various other sources. The park is known to be for the success of the species in Lagoinha are discussed. a refuge for the wildlife of large aquatic vertebrates, including populations of Capybaras (Hydrochoreus hydrochaeris) and Key words. -
Population Dynamics of <Emphasis Type="Italic">Moina Micrura
Proc, Indian Acad. Sci. (Anim, Sci.), Vol. 98, No.3, May 1989, pp. 211-222. © Printed in India. Population dynamics of Moina micrurs Kurz (Cladocera: Moinidae) inhabiting a eutrophic pond of Madurai (south India)* N MURUGAN Department of Zoology, Madura College, Madurai 625011. India MS received 13 July 1988; revised 10 March 1989 Abstract. Population density, composition, age structure and fecundity of Moina micrura have been studied in a eutrophic pond. The average clutch size of this species ranged from 1-4-4 eggs. The relationship between mean brood size and body length has been established. The volume of parthenogenetic eggs of this cladoceran ranges between 0·2 and 0·9 millions JL J and the adaptive significance of this has been discussed. The mean instantaneous birth rate which preceded maximum density of population resulted in a value of more than one. Keywords. Moina micrura; population density; composition; age structure; fecundity; egg volume. l. Introduction Moina micrura, a member of the family Moinidae primarily inhabits astatic ponds and pools in tropical and subtropical regions. This species is highly adapted to survive frequent dry periods and propagate rapidly in newly formed ponds. The review of literature on zooplankton species of Moina shows that the information about the population dynamics of M. micrura from tropical Indian waters is far from complete. Hence, an attempt has been made to investigate its population density and composition, fecundity and age structure in natural habitats. 2. Study area The present study was carried out in a seasonal shallow pond (figure 1) located in the Madura College campus at Madurai (Long: 78'8' E; Lat: 9'56' N), south India. -
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. -
Biology and Conservation of the Unique and Diverse Halophilic Macroinvertebrates of Australian Salt Lakes
CSIRO PUBLISHING Marine and Freshwater Research Corrigendum https://doi.org/10.1071/MF21088_CO Biology and conservation of the unique and diverse halophilic macroinvertebrates of Australian salt lakes Angus D’Arcy Lawrie, Jennifer Chaplin and Adrian Pinder Marine and Freshwater Research. [Published online 2 July 2021]. https://doi.org/10.1071/MF21088 The authors of the above-mentioned paper regret to inform readers that there were errors published in the systematics of one of the taxa in the manuscript. The list of groups in the Cladocera section (on p. F) was published as below: The bulk of Cladocera that occur in inland waters in Australia are restricted to fresh water, but three groups have representatives in salt lakes. These groups comprise: (1) six species of Daphniopsis (or Daphnia; see below); (2) two species of Daphnia (Daphnia salinifera Hebert and Daphnia neosalinifera Hebert) from the Daphnia carinata (King) subgenus; and (3) three species of chydorid: Moina baylyi Forro´, Moina mongolica Daday and Extremalona timmsi Sinev & Shiel. This text should have been as below (changes underlined): The bulk of Cladocera that occur in inland waters in Australia are restricted to fresh water, but four groups have representatives in salt lakes. These groups comprise: (1) six species of Daphniopsis (or Daphnia; see below); (2) two species of Daphnia (Daphnia salinifera Hebert and Daphnia neosalinifera Hebert) from the Daphnia carinata (King) subgenus; (3) two Moina species (Moina baylyi Forro´ and Moina mongolica Daday); and (4) one species of chydorid (Extremalona timmsi Sinev & Shiel). Furthermore, the title of the Chydorids section should have been titled Moinids and chydorids. -
Diversity and Density of Cladoceran Population in Different Types Of
Journal of Entomology and Zoology Studies 2017; 5(3): 1568-1572 E-ISSN: 2320-7078 P-ISSN: 2349-6800 Diversity and density of cladoceran population in JEZS 2017; 5(3): 1568-1572 © 2017 JEZS different types of water bodies of Ludhiana, Received: 04-03-2017 Accepted: 05-04-2017 Punjab (India) Ankita Thakur Ph.D Scholar, Department of Zoology, Punjab Agricultural Ankita Thakur and Devinder Kaur Kocher University, Ludhiana, Punjab, India Abstract The present study was conducted to record the diversity and density of cladoceran population during the Devinder Kaur Kocher year 2015. Water samples were collected from different types of water bodies viz; village ponds, fish Associate Professor, Department of Zoology, Punjab Agricultural ponds and paddy fields of Ludhiana, Punjab (India). Identification of cladocerans was done on the basis University, Ludhiana, Punjab, of morphological features and their enumeration with the help of Sedgewick-Rafter counting chamber (S- India R cell). Out of the recorded nine species of cladocerans, six were found to belong to family Daphnidae, two to family Moinidae and only one to family Chydoridae. Average percent composition of cladocerans in village ponds showed the distribution pattern with predominance of Daphnidae (51.01%) > Moinidae (48.27%) > Chydoridae (0.68%). In fish ponds Moinidae family was found to be predominant (62.95%) > Daphnidae (34.61%) > chydoridae (1.29%). Paddy fields were represented by Moinidae family only. Keywords: Cladocerans, density, diversity, water bodies 1. Introduction Among aquatic biota, freshwater zooplankton community comprises of protozoans, rotifers, cladocerans, copepods and ostracods. Out of these, cladocera is an ancient group of palaeozoic [6] origin and found in almost all kind of aquatic habitats. -
An Overview of the Contribution of Studies with Cladocerans
Acta Limnologica Brasiliensia, 2015, 27(2), 145-159 http://dx.doi.org/10.1590/S2179-975X3414 An overview of the contribution of studies with cladocerans to environmental stress research Um panorama da contribuição de estudos com cladóceros para as pesquisas sobre o estresse ambiental Albert Luiz Suhett1, Jayme Magalhães Santangelo2, Reinaldo Luiz Bozelli3, Christian Eugen Wilhem Steinberg4 and Vinicius Fortes Farjalla3 1Unidade Universitária de Biologia, Centro Universitário Estadual da Zona Oeste – UEZO, CEP 23070-200, Rio de Janeiro, RJ, Brazil e-mail: [email protected] 2Departamento de Ciências Ambientais, Instituto de Florestas, Universidade Federal Rural do Rio de Janeiro – UFRRJ, CEP 23890-000, Seropédica, RJ, Brazil e-mail: [email protected] 3Departamento de Ecologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro – UFRJ, CEP 21941-590, Rio de Janeiro, RJ, Brazil e-mail: [email protected]; [email protected] 4Institute of Biology, Faculty of Mathematics and Natural Sciences I, Humboldt Universität zu Berlin, 12437, Berlin, Germany e-mail: [email protected] Abstract: Cladocerans are microcrustaceans component of the zooplankton in a wide array of aquatic ecosystems. These organisms, in particular the genusDaphnia , have been widely used model organisms in studies ranging from biomedical sciences to ecology. Here, we present an overview of the contribution of studies with cladocerans to understanding the consequences at different levels of biological organization of stress induced by environmental factors. We discuss how some characteristics of cladocerans (e.g., small body size, short life cycles, cyclic parthenogenesis) make them convenient models for such studies, with a particular comparison with other major zooplanktonic taxa. -
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 -
Keys to the Australian Clam Shrimps (Crustacea: Branchiopoda: Laevicaudata, Spinicaudata, Cyclestherida)
Museum Victoria Science Reports 20: 1-25 (2018) ISSN 1833-0290 https://museumsvictoria.com.au/collections-research/journals/museum-victoria-science-reports/ https://doi.org/10.24199/j.mvsr.2018.20 Keys to the Australian clam shrimps (Crustacea: Branchiopoda: Laevicaudata, Spinicaudata, Cyclestherida) Brian V. Timms Honorary Research Associate, Australian Museum, 1 William Street, Sydney 2001; and Centre for Ecosystem Science, School of Biology, Earth and Environmental Sciences, University of New South Wales, Kensington, NSW 2052 Brian V. Timms. 2018. Keys to the Australian clam shrimps (Crustacea: Branchiopoda: Laevicau- data, Spinicaudata, Cyclestherida). Museum Victoria Science Reports 20: 1-25. Abstract The morphology and systematics of clam shrimps is described followed by a key to genera. Each genus is treated, including diagnostic features, list of species with distributions, and references provided to papers with keys or if these are not available preliminary keys to species within that genus are included. Keywords gnammas, freshwater, crustaceans, morphology Figure 1: Limnadopsis birchii – Worlds largest clam shrimp. Keys to the Australian clam shrimps Introduction Australia has a diverse clam shrimp fauna with about 78 species in nine genera recognised in 2017 (Rogers et al., 2012; Timms, 2012, 2013; Schwentner et al., 2012a,b, 2013a,b, 2015b,a; Timms & Schwentner, 2017; Tippelt & Schwent- ner, 2018) . This is an explosion from 26 species in 2008 (Richter & Timms, 2005; Brendonck et al., 2008) when Australia‘s proportion of the world fauna was about 15%; now it is about 30%. It is anticipated another five species will be described before 2020. There have been two periods of active re- search on Australian clam shrimps, the first Figure 2: Number of known species of Aus- from 1855 to 1927 with a peak around the turn tralian clam shrimps over time.