Efficacy of a Baiting Technique to Control Feral Cats on Christmas Island
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The Revised Classification of Eukaryotes
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/231610049 The Revised Classification of Eukaryotes Article in Journal of Eukaryotic Microbiology · September 2012 DOI: 10.1111/j.1550-7408.2012.00644.x · Source: PubMed CITATIONS READS 961 2,825 25 authors, including: Sina M Adl Alastair Simpson University of Saskatchewan Dalhousie University 118 PUBLICATIONS 8,522 CITATIONS 264 PUBLICATIONS 10,739 CITATIONS SEE PROFILE SEE PROFILE Christopher E Lane David Bass University of Rhode Island Natural History Museum, London 82 PUBLICATIONS 6,233 CITATIONS 464 PUBLICATIONS 7,765 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Biodiversity and ecology of soil taste amoeba View project Predator control of diversity View project All content following this page was uploaded by Smirnov Alexey on 25 October 2017. The user has requested enhancement of the downloaded file. The Journal of Published by the International Society of Eukaryotic Microbiology Protistologists J. Eukaryot. Microbiol., 59(5), 2012 pp. 429–493 © 2012 The Author(s) Journal of Eukaryotic Microbiology © 2012 International Society of Protistologists DOI: 10.1111/j.1550-7408.2012.00644.x The Revised Classification of Eukaryotes SINA M. ADL,a,b ALASTAIR G. B. SIMPSON,b CHRISTOPHER E. LANE,c JULIUS LUKESˇ,d DAVID BASS,e SAMUEL S. BOWSER,f MATTHEW W. BROWN,g FABIEN BURKI,h MICAH DUNTHORN,i VLADIMIR HAMPL,j AARON HEISS,b MONA HOPPENRATH,k ENRIQUE LARA,l LINE LE GALL,m DENIS H. LYNN,n,1 HILARY MCMANUS,o EDWARD A. D. -
Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes
University of Rhode Island DigitalCommons@URI Biological Sciences Faculty Publications Biological Sciences 9-26-2018 Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes Christopher E. Lane Et Al Follow this and additional works at: https://digitalcommons.uri.edu/bio_facpubs Journal of Eukaryotic Microbiology ISSN 1066-5234 ORIGINAL ARTICLE Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes Sina M. Adla,* , David Bassb,c , Christopher E. Laned, Julius Lukese,f , Conrad L. Schochg, Alexey Smirnovh, Sabine Agathai, Cedric Berneyj , Matthew W. Brownk,l, Fabien Burkim,PacoCardenas n , Ivan Cepi cka o, Lyudmila Chistyakovap, Javier del Campoq, Micah Dunthornr,s , Bente Edvardsent , Yana Eglitu, Laure Guillouv, Vladimır Hamplw, Aaron A. Heissx, Mona Hoppenrathy, Timothy Y. Jamesz, Anna Karn- kowskaaa, Sergey Karpovh,ab, Eunsoo Kimx, Martin Koliskoe, Alexander Kudryavtsevh,ab, Daniel J.G. Lahrac, Enrique Laraad,ae , Line Le Gallaf , Denis H. Lynnag,ah , David G. Mannai,aj, Ramon Massanaq, Edward A.D. Mitchellad,ak , Christine Morrowal, Jong Soo Parkam , Jan W. Pawlowskian, Martha J. Powellao, Daniel J. Richterap, Sonja Rueckertaq, Lora Shadwickar, Satoshi Shimanoas, Frederick W. Spiegelar, Guifre Torruellaat , Noha Youssefau, Vasily Zlatogurskyh,av & Qianqian Zhangaw a Department of Soil Sciences, College of Agriculture and Bioresources, University of Saskatchewan, Saskatoon, S7N 5A8, SK, Canada b Department of Life Sciences, The Natural History Museum, Cromwell Road, London, SW7 5BD, United Kingdom -
Redalyc.Studies on Coccidian Oocysts (Apicomplexa: Eucoccidiorida)
Revista Brasileira de Parasitologia Veterinária ISSN: 0103-846X [email protected] Colégio Brasileiro de Parasitologia Veterinária Brasil Pereira Berto, Bruno; McIntosh, Douglas; Gomes Lopes, Carlos Wilson Studies on coccidian oocysts (Apicomplexa: Eucoccidiorida) Revista Brasileira de Parasitologia Veterinária, vol. 23, núm. 1, enero-marzo, 2014, pp. 1- 15 Colégio Brasileiro de Parasitologia Veterinária Jaboticabal, Brasil Available in: http://www.redalyc.org/articulo.oa?id=397841491001 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Review Article Braz. J. Vet. Parasitol., Jaboticabal, v. 23, n. 1, p. 1-15, Jan-Mar 2014 ISSN 0103-846X (Print) / ISSN 1984-2961 (Electronic) Studies on coccidian oocysts (Apicomplexa: Eucoccidiorida) Estudos sobre oocistos de coccídios (Apicomplexa: Eucoccidiorida) Bruno Pereira Berto1*; Douglas McIntosh2; Carlos Wilson Gomes Lopes2 1Departamento de Biologia Animal, Instituto de Biologia, Universidade Federal Rural do Rio de Janeiro – UFRRJ, Seropédica, RJ, Brasil 2Departamento de Parasitologia Animal, Instituto de Veterinária, Universidade Federal Rural do Rio de Janeiro – UFRRJ, Seropédica, RJ, Brasil Received January 27, 2014 Accepted March 10, 2014 Abstract The oocysts of the coccidia are robust structures, frequently isolated from the feces or urine of their hosts, which provide resistance to mechanical damage and allow the parasites to survive and remain infective for prolonged periods. The diagnosis of coccidiosis, species description and systematics, are all dependent upon characterization of the oocyst. Therefore, this review aimed to the provide a critical overview of the methodologies, advantages and limitations of the currently available morphological, morphometrical and molecular biology based approaches that may be utilized for characterization of these important structures. -
Protista (PDF)
1 = Astasiopsis distortum (Dujardin,1841) Bütschli,1885 South Scandinavian Marine Protoctista ? Dingensia Patterson & Zölffel,1992, in Patterson & Larsen (™ Heteromita angusta Dujardin,1841) Provisional Check-list compiled at the Tjärnö Marine Biological * Taxon incertae sedis. Very similar to Cryptaulax Skuja Laboratory by: Dinomonas Kent,1880 TJÄRNÖLAB. / Hans G. Hansson - 1991-07 - 1997-04-02 * Taxon incertae sedis. Species found in South Scandinavia, as well as from neighbouring areas, chiefly the British Isles, have been considered, as some of them may show to have a slightly more northern distribution, than what is known today. However, species with a typical Lusitanian distribution, with their northern Diphylleia Massart,1920 distribution limit around France or Southern British Isles, have as a rule been omitted here, albeit a few species with probable norhern limits around * Marine? Incertae sedis. the British Isles are listed here until distribution patterns are better known. The compiler would be very grateful for every correction of presumptive lapses and omittances an initiated reader could make. Diplocalium Grassé & Deflandre,1952 (™ Bicosoeca inopinatum ??,1???) * Marine? Incertae sedis. Denotations: (™) = Genotype @ = Associated to * = General note Diplomita Fromentel,1874 (™ Diplomita insignis Fromentel,1874) P.S. This list is a very unfinished manuscript. Chiefly flagellated organisms have yet been considered. This * Marine? Incertae sedis. provisional PDF-file is so far only published as an Intranet file within TMBL:s domain. Diplonema Griessmann,1913, non Berendt,1845 (Diptera), nec Greene,1857 (Coel.) = Isonema ??,1???, non Meek & Worthen,1865 (Mollusca), nec Maas,1909 (Coel.) PROTOCTISTA = Flagellamonas Skvortzow,19?? = Lackeymonas Skvortzow,19?? = Lowymonas Skvortzow,19?? = Milaneziamonas Skvortzow,19?? = Spira Skvortzow,19?? = Teixeiromonas Skvortzow,19?? = PROTISTA = Kolbeana Skvortzow,19?? * Genus incertae sedis. -
A New Framework for the Study of Apicomplexan Diversity Across Environments
bioRxiv preprint doi: https://doi.org/10.1101/494880; this version posted December 12, 2018. 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 4.0 International license. An Original Article submitted to PLoS Pathogens A new framework for the study of apicomplexan diversity across environments Javier del Campo1,2*, Thierry Heger1,3, Raquel Rodríguez-Martínez4, Alexandra Z. Worden5, Thomas A. Richards4, Ramon Massana2 and Patrick J. Keeling1* 1University of British Columbia, 3529-6270 University Boulevard, Vancouver, BC, V6T 1Z4, Canada. 2Department of Marine Biology and Oceanography, Institut de Ciències del Mar (CSIC), Barcelona, Catalonia, Spain 3Soil Science Group, CHANGINS, University of Applied Sciences and Arts Western Switzerland, Nyon, Switzerland 4Living Systems Institute, Biosciences, College of Life and Environmental Sciences, University of Exeter, Stocker Road, Exeter, EX4 4QD, UK 5Monterey Bay Aquarium Research Institute, Moss Landing, CA 95039, US *Corresponding authors: University of British Columbia, 3529-6270 University Boulevard, Vancouver, BC, V6T 1Z4, Canada. Phone +1 (604) 822-2845; Fax: +1 (604) 822-6089; E- mail: [email protected] / [email protected] bioRxiv preprint doi: https://doi.org/10.1101/494880; this version posted December 12, 2018. 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 4.0 International license. Abstract Apicomplexans are a group of microbial eukaryotes that contain some of the most well- studied parasites, including widespread intracellular pathogens of mammals such as Toxoplasma and Plasmodium (the agent of malaria), and emergent pathogens like Cryptosporidium and Babesia. -
The Revised Classification of Eukaryotes
Published in Journal of Eukaryotic Microbiology 59, issue 5, 429-514, 2012 which should be used for any reference to this work 1 The Revised Classification of Eukaryotes SINA M. ADL,a,b ALASTAIR G. B. SIMPSON,b CHRISTOPHER E. LANE,c JULIUS LUKESˇ,d DAVID BASS,e SAMUEL S. BOWSER,f MATTHEW W. BROWN,g FABIEN BURKI,h MICAH DUNTHORN,i VLADIMIR HAMPL,j AARON HEISS,b MONA HOPPENRATH,k ENRIQUE LARA,l LINE LE GALL,m DENIS H. LYNN,n,1 HILARY MCMANUS,o EDWARD A. D. MITCHELL,l SHARON E. MOZLEY-STANRIDGE,p LAURA W. PARFREY,q JAN PAWLOWSKI,r SONJA RUECKERT,s LAURA SHADWICK,t CONRAD L. SCHOCH,u ALEXEY SMIRNOVv and FREDERICK W. SPIEGELt aDepartment of Soil Science, University of Saskatchewan, Saskatoon, SK, S7N 5A8, Canada, and bDepartment of Biology, Dalhousie University, Halifax, NS, B3H 4R2, Canada, and cDepartment of Biological Sciences, University of Rhode Island, Kingston, Rhode Island, 02881, USA, and dBiology Center and Faculty of Sciences, Institute of Parasitology, University of South Bohemia, Cˇeske´ Budeˇjovice, Czech Republic, and eZoology Department, Natural History Museum, London, SW7 5BD, United Kingdom, and fWadsworth Center, New York State Department of Health, Albany, New York, 12201, USA, and gDepartment of Biochemistry, Dalhousie University, Halifax, NS, B3H 4R2, Canada, and hDepartment of Botany, University of British Columbia, Vancouver, BC, V6T 1Z4, Canada, and iDepartment of Ecology, University of Kaiserslautern, 67663, Kaiserslautern, Germany, and jDepartment of Parasitology, Charles University, Prague, 128 43, Praha 2, Czech -
Adl S.M., Simpson A.G.B., Lane C.E., Lukeš J., Bass D., Bowser S.S
The Journal of Published by the International Society of Eukaryotic Microbiology Protistologists J. Eukaryot. Microbiol., 59(5), 2012 pp. 429–493 © 2012 The Author(s) Journal of Eukaryotic Microbiology © 2012 International Society of Protistologists DOI: 10.1111/j.1550-7408.2012.00644.x The Revised Classification of Eukaryotes SINA M. ADL,a,b ALASTAIR G. B. SIMPSON,b CHRISTOPHER E. LANE,c JULIUS LUKESˇ,d DAVID BASS,e SAMUEL S. BOWSER,f MATTHEW W. BROWN,g FABIEN BURKI,h MICAH DUNTHORN,i VLADIMIR HAMPL,j AARON HEISS,b MONA HOPPENRATH,k ENRIQUE LARA,l LINE LE GALL,m DENIS H. LYNN,n,1 HILARY MCMANUS,o EDWARD A. D. MITCHELL,l SHARON E. MOZLEY-STANRIDGE,p LAURA W. PARFREY,q JAN PAWLOWSKI,r SONJA RUECKERT,s LAURA SHADWICK,t CONRAD L. SCHOCH,u ALEXEY SMIRNOVv and FREDERICK W. SPIEGELt aDepartment of Soil Science, University of Saskatchewan, Saskatoon, SK, S7N 5A8, Canada, and bDepartment of Biology, Dalhousie University, Halifax, NS, B3H 4R2, Canada, and cDepartment of Biological Sciences, University of Rhode Island, Kingston, Rhode Island, 02881, USA, and dBiology Center and Faculty of Sciences, Institute of Parasitology, University of South Bohemia, Cˇeske´ Budeˇjovice, Czech Republic, and eZoology Department, Natural History Museum, London, SW7 5BD, United Kingdom, and fWadsworth Center, New York State Department of Health, Albany, New York, 12201, USA, and gDepartment of Biochemistry, Dalhousie University, Halifax, NS, B3H 4R2, Canada, and hDepartment of Botany, University of British Columbia, Vancouver, BC, V6T 1Z4, Canada, and iDepartment -
A Coccidian Parasite of the Kidney of Blue Missels, Species of Mytilus, from British Columbia, Canada
Article available at http://www.parasite-journal.org or http://dx.doi.org/10.1051/parasite/1998051017 PSEUDOKLOSSIA SEMILUNA N. SP. (APICOMPLEXA: AGGREGATIDAE): A COCCIDIAN PARASITE OF THE KIDNEY OF BLUE MISSELS, SPECIES OF MYTILUS, FROM BRITISH COLUMBIA, CANADA DESSER S.S.*, BOWER S.M.** & HONG H.* Summary : RÉSUMÉ : PSEUDOKLOSSIA SEMILUNA N. SP. (APICOMPLEXA: AGGREGATIDAE): COCCIDIE RÉNALE DES MOULES BLEUES, ESPÈCES DE MYTILUS, EN COLOMBIE Three of 91 mussels, taken from Pacific coastal waters in BRITANNIQUE (CANADA) Nanaimo, British Columbia, were infected with a new species of coccidian parasite. Gamogonic and sporogonic development Sur un groupe de 91 moules récollées sur la côte Pacifique, à were observed in renal tubular epithelial cells. Mature Nanaimo (Colombie Britannique), trois étaient infectées par une macrogametocytes were crescent-shaped. Oocysts sporulated nouvelle espèce de coccidie. La gamogonie et la sporogonie within the host. Mature oocysts were spherical, mean 23.9 μm s'effectuent dans les cellules épithéliales des tubules rénaux. Les (range 22-25 μm| with approximately 24 ellipsoidal sporocysts macrogamétocytes mûrs sont en forme de croissant. Les oocystes (approximately 6x3 μm), each of which contained two sporulent dans l'hôte. Les oocystes mûrs sont sphériques, mesurent sporozoites. Ultrastructural features of immature and mature 23,9 μm (22-25 μm) de diamètre et ont 24 sporocystes macrogametocytes are described. Although found in all five ellipsoïdaux, d'environ 6x 3 mm, contenant chacun deux populations of mussels from various locations in British Columbia, sporozoïtes. Description et interprétation des caractéristiques prevalence of infection was usually less than 16%, intensity of ultrastructurales des macrogamétocytes mûrs et immatures. -
INFECTING the FRESH WATER SNAIL PIRENELLA CONICA LIGHT and ELECTRON MICROSCOPE STUDIES by HODA M
Journal of the Egyptian Society of Parasitology, Vol.44, No.2, August 2014 J. Egypt. Soc. Parasitol. (JESP), 44(2), 2014: 435 -446 PFEIFFERINELLA SP. (PFEIFFERINELLIDAE, APICOMPLEXA) INFECTING THE FRESH WATER SNAIL PIRENELLA CONICA LIGHT AND ELECTRON MICROSCOPE STUDIES By HODA M. EL-FAYOMI, HAYAM MOHAMMED AND THABET SAKRAN Department of Zoology, Faculty of Science, Beni Suef University, Beni Suef, Egypt Abstract Coccidian oocysts were proved to be found in 70 of 100 collected Pirenella conica snails, with a natural infection of 70%. It was observed that, Pfeifferinella sp. was transferred between hepatopancreas and small intestine of snail. The prepatent period of Pfeifferinella sp. infecting P. conica snails ranged from 14-18 days and the patent period was reached 50 days (P.I.). Mer- ogony stages were the early stages observed in this study. These stages were observed in the hepatopancreas and in a large clear parasiteophorous vacuole (PV). In snails killed 4 days P.I. immature meronts were measured 12 х 10 µm containing 8 nuclei. Meanwhile, mature meronts with about 6 differentiated merozoites were detected as early as 6 days P.I., and measured 3.1х1.4µm. The earliest gametogonic stages were seen in the intestine of Pirenella conica snails killed 12 days P.I. Microgamonts contained about 4 nuclei and measured 7.9х6.7µm. The mac- rogamonts measured 7.3х5.6µm. Macrogametes were characterized by the presence of the vagi- nal tube, this tube measured 4.3х1.1µm. Fertilization was occurred in the intestine of the infect- ed snails at 12 days P.I. Zygotes developed into young oocysts after fertilization. -
Systematic Revision of the Adeleid Haemogregarines, with Creation of Bartazoon N
Parasite 2015, 22,31 Ó G. Karadjian et al., published by EDP Sciences, 2015 DOI: 10.1051/parasite/2015031 urn:lsid:zoobank.org:pub:DF980FF6-3F2A-4A77-A873-0C9C70A1FDFF Available online at: www.parasite-journal.org RESEARCH ARTICLE OPEN ACCESS Systematic revision of the adeleid haemogregarines, with creation of Bartazoon n. g., reassignment of Hepatozoon argantis Garnham, 1954 to Hemolivia, and molecular data on Hemolivia stellata Grégory Karadjian1,a, Jean-Marc Chavatte2,a, and Irène Landau1,* 1 UMR 7245 MCAM MNHN CNRS, Muséum National d’Histoire Naturelle, 61 rue Buffon, CP 52, 75231 Paris Cedex 05, France 2 Malaria Reference Centre – National Public Health Laboratory, Ministry of Health, 3 Biopolis Drive, Synapse #05-14/16, Singapore 138623 Received 19 March 2015, Accepted 14 October 2015, Published online 9 November 2015 Abstract – Life cycles and molecular data for terrestrial haemogregarines are reviewed in this article. Collection material was re-examined: Hepatozoon argantis Garnham, 1954 in Argas brumpti was reassigned to Hemolivia as Hemolivia argantis (Garnham, 1954) n. comb.; parasite DNA was extracted from a tick crush on smear of an archived slide of Hemolivia stellata in Amblyomma rotondatum, then the 18S ssrRNA gene was amplified by PCR. A system- atic revision of the group is proposed, based on biological life cycles and phylogenetic reconstruction. Four types of life cycles, based on parasite vector, vertebrate host and the characteristics of their development, are defined. We pro- pose combining species, based on their biology, into four groups (types I, II, III and IV). The characters of each type are defined and associated with a type genus and a type species. -
Assessing the Diversity and Distribution of Apicomplexans In
fmicb-10-02373 October 7, 2020 Time: 15:20 # 1 ORIGINAL RESEARCH published: 23 October 2019 doi: 10.3389/fmicb.2019.02373 Assessing the Diversity and Distribution of Apicomplexans in Host and Free-Living Environments Using High-Throughput Amplicon Data and a Phylogenetically Informed Reference Framework Javier del Campo1,2*, Thierry J. Heger1,3, Raquel Rodríguez-Martínez4, Alexandra Z. Worden5, Thomas A. Richards4, Ramon Massana6 and Patrick J. Keeling1* Edited by: 1 Department of Botany, University of British Columbia, Vancouver, BC, Canada, 2 Department of Marine Biology Ludmila Chistoserdova, and Ecology, Rosenstiel School of Marine and Atmospheric Science, University of Miami, Miami, FL, United States, 3 Soil University of Washington, Science Group, CHANGINS, University of Applied Sciences and Arts Western Switzerland, Nyon, Switzerland, 4 Department United States of Biosciences, Living Systems Institute, College of Life and Environmental Sciences, University of Exeter, Exeter, United Kingdom, 5 GEOMAR – Helmholtz Centre for Ocean Research Kiel, Kiel, Germany, 6 Department of Marine Biology Reviewed by: and Oceanography, Institut de Ciències del Mar (CSIC), Barcelona, Spain Isabelle Florent, Muséum National d’Histoire Naturelle, France Apicomplexans are a group of microbial eukaryotes that contain some of the most Jane Carlton, New York University, United States well-studied parasites, including the causing agents of toxoplasmosis and malaria, *Correspondence: and emergent diseases like cryptosporidiosis or babesiosis. Decades of research have Javier del Campo illuminated the pathogenic mechanisms, molecular biology, and genomics of model [email protected]; apicomplexans, but we know little about their diversity and distribution in natural [email protected] Patrick J. Keeling environments. In this study we analyze the distribution of apicomplexans across a [email protected] range of both host-associated and free-living environments. -
Cercozoa Apusozoa Heliozoa Phytomyxids Haplosporidia Filosa Foraminifera Radiolaria Opisthokonts Fungi
PROTISTS GROUPS (ref. 1) Cercozoa Apusozoa Heliozoa Phytomyxids Haplosporidia Filosa Foraminifera Radiolaria Opisthokonts Fungi Animals Nuclearids Ichthyosporea Choanoflagellates Amoebozoa Lobosea Slime Molds Archamoebae Excavates Oxymonads Trimastix Hypermastigotes Trichomonads Retortamonads Diplomonads Carpediamonas Jakobids (core) Discicristates Kinetoplastids Diplonemids Euglenids Heterolobosea Chromists Cryptomonads Haptophytes Opalinids Bicosoecids Oomycetes Diatoms Brown Algae Alveolates Ciliates Colpodellids Apicomplexa Dinoflagellates Oxyrrhis Perkinsus Plantae Plants (Plants and other autotrophs ignored.) Charophytes Chlorophytes Red Algae Glaucophytes SUMMARY: NUMBER OF SPECIES IN EACH GROUP CONTAINING INFORMATION ON PLOIDY AND LIFE STYLE Diploid Parasite (~1468-1963 species) Some Lobosea (<10 species?, ref. 2, p. 7-8) Some Diplomonads (~8 species, ref. 2, p. 202) Some Trypanosomes (unknown fraction of ~495 species are diploid, ref. 2, p. 218) Some Oomycetes (>250 species, ref. 2, p. 672-678) Some Ciliates (~1200 species; ref. 3, p. 40) Haploid Parasite (~2573-3068 species) All Phytomyxids (~29 species, ref. 2, p. 399) Some Trichomonads (~4 species, ref. 4) Some Trypanosomes (unknown fraction of ~495 species are haploid, ref. 2, p. 218) All Apicomplexa (~2400 species, ref. 2, p. 549) Some Dinoflagellates (~140 species, ref. 5, p. 1) Diploid Non-Parasite (~7284 species) All Heliozoa (~90 species, ref. 2, p. 347) Most Lobosea (~200 species, ref. 2, p. 3) Some Oxymonads (~20 species, ref. 6) Some Hypermastigotes (~4 species, ref. 6) Most Diplomonads (~100 species, ref. 2, p. 202) Most Ciliates (>6300 species = 85% of 7500, ref. 2, p. 498) All Opalinids (~400 species, ref. 2, p. 239) Some Oomycetes (>170 species, ref. 2, p. 672-678) Haploid Non-Parasite (~1465 species) Dictyostelium (~50 species, ref. 2, p.