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7 Blastocladiomycota

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Systematics and Evolution

Part of the book series: The Mycota ((MYCOTA,volume 7A))

Abstract

The Blastocladiomycota (blastoclads) are a phylum of zoosporic fungi that include diverse taxa such as the model water mold Allomyces. The 14 genera of blastoclads form a monophyletic group that is phylogenetically distinct from other Fungi and unique in having an alternation of haploid and diploid generations. Blastoclads can be distinguished from other zoosporic true fungi (e.g., Chytridiomycota) on the basis of the ultrastructure of their uniflagellated zoospores. These ultrastructural characters are also taxonomically informative at the generic level. The precise placement of Blastocladiomycota in the fungal tree of life is uncertain but has a large bearing on the evolution of several traits, such as an intact nuclear envelope during mitosis and heterothallism with mating types. Environmental DNA studies suggest that blastoclads may be enriched in suboxic or anaerobic environments, and although some species are known to be obligate fermenters, none is known to be obligately anaerobic.

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References

  • Barner HD, Cantino EC (1952) Nutritional relationships in a new species of Blastocladiella. Am J Bot 39:746–751

    CAS  Google Scholar 

  • Barr DJS, Hartmann VE (1976) Zoospore ultrastructure of three Chytridium species and Rhizoclosmatium globosum. Can J Bot 54:2000–2013

    Google Scholar 

  • Barstow WE, Lovett JS (1975) Formation of gamma-particles during zoosporogenesis in Blastocladiella emersonii. Mycologia 67:518–529

    CAS  PubMed  Google Scholar 

  • Barstow WE, Pommerville J (1980) The ultrastructure of cell wall formation and of gamma-particles during encystment of Allomyces macrogynus zoospores. Arch Microbiol 128:179–189

    Google Scholar 

  • Bendich AJ (1993) Reaching for the ring: the study of mitochondrial genome structure. Curr Genet 24:279–290

    CAS  PubMed  Google Scholar 

  • Bendich AJ (1996) Structural analysis of mitochondrial DNA molecules from Fungi and Plants using moving pictures and pulsed-field gel elctrophoresis. J Mol Biol 255:564–588

    CAS  PubMed  Google Scholar 

  • Bendich AJ (2010) The end of the circle for yeast mitochondrial DNA. Mol Cell 39:831–832

    CAS  PubMed  Google Scholar 

  • Bland CE (1985) Culture. In: Couch JN, Bland CE (eds) The genus Coelomomyces. Academic, Orlando, FL, pp 349–359

    Google Scholar 

  • Borkhardt B, Delius H (1983) Physical map of the mitochondrial DNA from the phycomycete Allomyces macrogynus including the position of the ribosomal RNA genes and of an intervening sequence in the large rRNA gene. Curr Genet 7:327–333

    CAS  PubMed  Google Scholar 

  • Borkhardt B, Olson LW (1979) Meiotic prophase in diploid and tetraploid strains of Allomyces macrogynus. Protoplasma 100:323–343

    Google Scholar 

  • Borkhardt B, Olson LW (1986) The mitochondrial genome of the aquatic phycomycete Blastocladiella emersonii. Curr Genet 11:139–143

    CAS  Google Scholar 

  • Borkhardt B, Brown TA, Thim P, Olson LW (1988) The mitochondrial genome of the aquatic phycomycete Allomyces macrogynus. Physical mapping and mitochondrial DNA instability. Curr Genet 13:41–47

    CAS  Google Scholar 

  • Bowman BH, Taylor JW, Brownlee AG, Lee J, Lu SD, White TJ (1992) Molecular evolution of the fungi- relationship of the Basidiomycetes, Ascomycetes, and Chytridiomycetes. Mol Biol Evol 9:285–296

    CAS  PubMed  Google Scholar 

  • Brasier CM (2001) Rapid evolution of introduced plant pathogens via interspecific hybridization. Bioscience 51:123–133

    Google Scholar 

  • Brown MW, Spiegel FW, Silberman JD (2009) Phylogeny of the “forgotten” cellular slime mold, Fonticula alba, reveals a key evolutionary branch within Opisthokonta. Mol Biol Evol 26:2699–2709

    CAS  PubMed  Google Scholar 

  • Bruns TD, White TJ, Taylor JW (1991) Fungal molecular systematics. Annu Rev Ecol Syst 22:525–564

    Google Scholar 

  • Bruns TD, Vilgalys R, Barns SM, Gonzalez D, Hibbett DS, Lane DJ, Simon L, Stickel S, Szaro TM, Weisburg WG, Sogin ML (1992) Evolutionary relationships within the Fungi: analyses of nuclear small subunit rRNA sequences. Mol Phylogenet Evol 1:231–241

    CAS  PubMed  Google Scholar 

  • Bullerwell CE, Forget L, Lang BF (2003) Evolution of monoblepharidalean fungi based on complete mitochondrial genome sequences. Nucleic Acids Res 31:1614–1623

    CAS  PubMed Central  PubMed  Google Scholar 

  • Burger G, Forget L, Zhu Y, Gray MW, Lang BF (2003) Unique mitochondrial genome architecture in unicellular relatives of animals. Proc Natl Acad Sci USA 100:892–897

    CAS  PubMed Central  PubMed  Google Scholar 

  • Butler EJ (1911) On Allomyces, a new aquatic fungus. Ann Bot 25:1023–1035

    Google Scholar 

  • Cai L, Giraud T, Zhang N, Begerow D, Cai GH, Shivas RG (2011) The evolution of species concepts and species recognition criteria in plant pathogenic fungi. Fungal Divers 50:121–133

    Google Scholar 

  • Cantino EC (1956) The relation between cellular metabolism and morphogenesis in Blastocladiella. Mycologia 48:225–240

    Google Scholar 

  • Cantino EC, Horenstein EA (1954) Cytoplasmic exchange without gametic copulation in the water mold Blastocladiella emersonii. Am Nat 88:143–154

    Google Scholar 

  • Cantino EC, Hyatt MT (1953) Phenotypic “sex” determination in the life history of a new species of Blastocladiella, B emersonii. Antonie Van Leeuwenhoek 19:25–70

    CAS  PubMed  Google Scholar 

  • Cantino EC, Truesdell LC (1970) Organization and fine structure of side body and its lipid sac in zoospore of Blastocladiella emersonii. Mycologia 62:548–567

    CAS  PubMed  Google Scholar 

  • Cantino EC, Truesdell LC (1971) Cytoplasmic gamma-like particles and other ultrastructural aspects of zoospores of Blastocladiella britannica. Trans Br Mycol Soc 56:169–179

    Google Scholar 

  • Cantino EC, Turian GF (1959) Physiology and development of lower fungi (Phycomycetes). Annu Rev Microbiol 13:97–124

    Google Scholar 

  • Carlile MJ, Machlis L (1965) Response of male gametes of Allomyces to sexual hormone sirenin. Am J Bot 52:478–483

    CAS  Google Scholar 

  • Castillo JM, Roberts DW (1980) In vitro studies of Coelomomyces punctatus from Anopheles quadrimaculatus and Cyclops vernalis. J Invertebr Pathol 35:144–157

    Google Scholar 

  • Chapman HC (1985) Ecology and use of Coelomomyces species in biological control: a review. In: Couch JN, Bland CE (eds) The genus Coelomomyces. Academic, Orlando, FL, pp 361–368

    Google Scholar 

  • Chen MJ, Chen FZ, Yu Y, Ji J, Kong FX (2008) Genetic diversity of eukaryotic microorganisms in Lake Taihu, a large shallow subtropical lake in China. Microb Ecol 56:572–583

    CAS  PubMed  Google Scholar 

  • Couch JN (1945) Observations on the genus Catenaria. Mycologia 37:163–191

    Google Scholar 

  • Couch JN, Bland CE (1985) The genus Coelomomyces. Academic, New York

    Google Scholar 

  • Couch JN, Whiffen AJ (1942) Observations on the genus Blastocladiella. Am J Bot 29:582–591

    Google Scholar 

  • Crasemann JM (1957) Comparative nutrition of two species of Blastocladia. Am J Bot 44:218–224

    Google Scholar 

  • Dalley NE, Sonneborn DR (1982) Evidence that Blastocladiella emersonii zoospore chitin synthetase is located at the plasma membrane. Biochim Biophys Acta 686:65–76

    CAS  Google Scholar 

  • Dasgupta SN, John R (1988) A contribution to our knowledge of the genus Blastocladia. Indian Phytopathol 41:521–547

    Google Scholar 

  • Debaisieux P (1920) Coelomycidium simulii nov. gen., nov. sp. et remarques sur l’Amoebidium des larves de Simulium. Cellule 30:249–271

    Google Scholar 

  • DeSouza CPC, Osmani SA (2007) Mitosis, not just open or closed. Eukaryot Cell 6:1521–1527

    CAS  Google Scholar 

  • Dewel RA, Dewel WC (1990) The fine structure of the zoospore of Sorochytrium milnesiophthora. Can J Bot 68:1968–1977

    Google Scholar 

  • Dewel RA, Joines JD, Bond JJ (1985) A new chytridiomycete parasitizing the tardigrade Milnesium tardigradum. Can J Bot 63:1525–1534

    Google Scholar 

  • Doweld AB (2001) Prosyllabus tracheophytorum. Tentamen systematis plantarum vascularium (Tracheophyta). Geos, Moscow

    Google Scholar 

  • Emerson R (1938) A new life cycle involving cyst-formation in Allomyces. Mycologia 30:120–132

    Google Scholar 

  • Emerson R (1941) An experimental study of the life cycles and taxonomy of Allomyces. Lloydia 4:77–144

    Google Scholar 

  • Emerson R, Cantino EC (1948) The isolation, growth, and metabolism of Blastocladia in pure culture. Am J Bot 35:157–171

    CAS  Google Scholar 

  • Emerson R, Robertson JA (1974) Two new members of Blastocladiaceae. I. Taxonomy, with an evaluation of genera and interrelationships in family. Am J Bot 61:303–317

    Google Scholar 

  • Emerson R, Wilson CM (1949) The significance of meiosis in Allomyces. Science 110:86–88

    CAS  PubMed  Google Scholar 

  • Emerson R, Wilson CM (1954) Interspecific hybrids and the cytogenetics and cytotaxonomy of Euallomyces. Mycologia 46:393–434

    Google Scholar 

  • Federici BA (1979) Experimental hybridization of Coelomomyces dodgei and Coelomomyces punctatus. Proc Natl Acad Sci USA 76:4425–4428

    CAS  PubMed Central  PubMed  Google Scholar 

  • Federici BA (1982) Inviability of interspecific hybrids in the Coelomomyces dodgei complex. Mycologia 74:555–562

    Google Scholar 

  • Federici BA, Lucarotti CJ (1986) Structure and behavior of the meiospore of Coelomomyces dodgei during encystment on the copepod host, Acanthocyclops vernalis. J Invertebr Pathol 48:259–268

    CAS  PubMed  Google Scholar 

  • Fischer A (1892) Phycomycetes. Die Pilze Deutschlands, Oesterreichs und der Schweiz. Kryptogamen-Fl 1:1–490

    Google Scholar 

  • Förster H, Coffey MD, Elwood H, Sogin ML (1990) Sequence analysis of the small subunit ribosomal RNAs of three zoosporic fungi and implications for fungal evolution. Mycologia 82:306–312

    Google Scholar 

  • Freeman KR, Martin AP, Karki D, Lynch RC, Mitter MS, Meyer AF, Longcore JE, Simmons DR, Schmidt SK (2009) Evidence that chytrids dominate fungal communities in high-elevation soils. Proc Natl Acad Sci USA 106:18315–18320

    CAS  PubMed Central  PubMed  Google Scholar 

  • Fuller MS, Calhoun SA (1968) Microtubule-kinetosome relationships in motile cells of Blastocladiales. Z Zellforsch Mikrosk Anat 87:526–533

    CAS  PubMed  Google Scholar 

  • Fuller MS, Olson LW (1971) Zoospore of Allomyces. J Gen Microbiol 66:171–183

    Google Scholar 

  • Garcia R (1983) Mosquito management - ecological approaches. Environ Manage 7:73–78

    Google Scholar 

  • Gleason FH, Gordon GLR (1989) Anaerobic growth and fermentation in Blastocladia. Mycologia 81:811–815

    CAS  Google Scholar 

  • Gleason FH, Marano AV, Johnson P, Martin WW (2010) Blastocladian parasites of invertebrates. Fungal Biol Rev 24:56–67

    Google Scholar 

  • Griffiths AJF (1996) Mitochondrial inheritance in filamentous fungi. J Genet 75:403–414

    CAS  Google Scholar 

  • Harder R, Sörgel G (1938) Über einen neuen plano-isogamen Phycomyceten mit Generationswechel und seine phylogenetische Bedeutung. Nachrichten Gesell Wiss Göttingen Fachgruppe VI (Biol) 3:119–127

    Google Scholar 

  • Hatch WR (1935) Gametogenesis in Allomyces arbuscula. Ann Bot 49:623–649

    Google Scholar 

  • Heath IB (1980) Variant mitoses in lower eukaryotes: indicators of the evolution of mitosis? Int Rev Cytol 64:1–80

    CAS  PubMed  Google Scholar 

  • Held AA, Emerson R, Fuller MS, Gleason FH (1969) Blastocladia and Aqualinderella – fermentative water molds with high carbon dioxide optima. Science 165:706–709

    CAS  PubMed  Google Scholar 

  • Hibbett DS, Binder M, Bischoff JF, Blackwell M, Cannon PF, Eriksson OE, Huhndorf S, James T, Kirk PM, Lucking R, Lumbsch HT, Lutzoni F, Matheny PB, McLaughlin DJ, Powell MJ, Redhead S, Schoch CL, Spatafora JW, Stalpers JA, Vilgalys R, Aime MC, Aptroot A, Bauer R, Begerow D, Benny GL, Castlebury LA, Crous PW, Dai YC, Gams W, Geiser DM, Griffith GW, Gueidan C, Hawksworth DL, Hestmark G, Hosaka K, Humber RA, Hyde KD, Ironside JE, Koljalg U, Kurtzman CP, Larsson KH, Lichtwardt R, Longcore J, Miadlikowska J, Miller A, Moncalvo JM, Mozley-Standridge S, Oberwinkler F, Parmasto E, Reeb V, Rogers JD, Roux C, Ryvarden L, Sampaio JP, Schussler A, Sugiyama J, Thorn RG, Tibell L, Untereiner WA, Walker C, Wang Z, Weir A, Weiss M, White MM, Winka K, Yao YJ, Zhang N (2007) A higher-level phylogenetic classification of the Fungi. Mycol Res 111:509–547

    PubMed  Google Scholar 

  • Hill EP (1969) Fine structure of zoospores and cysts of Allomyces macrogynus. J Gen Microbiol 56:125–130

    CAS  PubMed  Google Scholar 

  • Hoffman Y, Aflalo C, Zarka A, Gutman J, James TY, Boussiba S (2008) Isolation and characterization of a novel chytrid species (phylum Blastocladiomycota), parasitic on the green alga Haematococcus. Mycol Res 112:70–81

    CAS  PubMed  Google Scholar 

  • Hohn TM, Lovett JS, Bracker CE (1984) Characterization of the major proteins in gamma particles, cytoplasmic organelles in Blastocladiella emersonii zoospores. J Bacteriol 158:253–263

    CAS  PubMed Central  PubMed  Google Scholar 

  • Horenstein EA, Cantino EC (1962) Dark-induced morphogenesis in synchronized cultures of Blastocladiella britannica. J Bacteriol 84:37–45

    CAS  PubMed Central  PubMed  Google Scholar 

  • Horgen PA, Meyer RJ, Franklin AL, Anderson JB, Filion WG (1985) Motile spores from resistant sporangia of Blastocladiella emersonii possess one-half the DNA of spores from ordinary colorless sporangia. Exp Mycol 9:70–73

    CAS  Google Scholar 

  • Ichida AA, Fuller MS (1968) Ultrastructure of mitosis in the aquatic fungus Catenaria anguillulae. Mycologia 60:141–155

    CAS  PubMed  Google Scholar 

  • Ingraham JL, Emerson R (1954) Studies of the nutrition and metabolism of the aquatic phycomycete, Allomyces. Am J Bot 41:146–152

    CAS  Google Scholar 

  • James TY, Porter D, Leander CA, Vilgalys R, Longcore JE (2000) Molecular phylogenetics of the Chytridiomycota supports the utility of ultrastructural data in chytrid systematics. Can J Bot 78:336–350

    CAS  Google Scholar 

  • James TY, Kauff F, Schoch C, Matheny PB, Hofstetter V, Cox C, Celio G, Gueidan C, Fraker E, Miadlikowska J, Lumbsch HT, Rauhut A, Reeb V, Arnold AE, Amtoft A, Stajich JE, Hosaka K, Sung G-H, Johnson D, O’Rourke B, Crockett M, Binder M, Curtis JM, Slot JC, Wang Z, Wilson AW, Schüßler A, Longcore JE, O’Donnell K, Mozley-Standridge S, Porter D, Letcher PM, Powell MJ, Taylor JW, White MM, Griffith GW, Davies DR, Humber RA, Morton JB, Sugiyama J, Rossman AY, Rogers JD, Pfister DH, Hewitt D, Hansen K, Hambleton S, Shoemaker RA, Kohlmeyer J, Volkmann-Kohlmeyer B, Spotts RA, Serdani M, Crous PW, Hughes KW, Matsuura K, Langer E, Langer G, Untereiner WA, Lücking R, Büdel B, Geiser DM, Aptroot A, Diederich P, Schmitt I, Schultz M, Yahr R, Hibbett D, Lutzoni F, McLaughlin D, Spatafora J, Vilgalys R (2006a) Reconstructing the early evolution of the fungi using a six gene phylogeny. Nature 443:818–822

    CAS  PubMed  Google Scholar 

  • James TY, Letcher PM, Longcore JE, Mozley-Standridge SE, Porter D, Powell MJ, Griffith GW, Vilgalys R (2006b) A molecular phylogeny of the flagellated fungi (Chytridiomycota) and description of a new phylum (Blastocladiomycota). Mycologia 98:860–871

    PubMed  Google Scholar 

  • James TY, Hoffman Y, Zarka A, Boussiba S (2011) Paraphysoderma sedebokerense, gen. et sp. nov., an aplanosporic relative of Physoderma (Blastocladiomycota). MycoTaxon 118:177–180

    Google Scholar 

  • Jaworski AJ, Stumhofer P (1984) Dormant ribosomes in Blastocladiella emersonii zoospores are arrested at elongation. Exp Mycol 8:13–24

    CAS  Google Scholar 

  • Johnson PTJ, Longcore JE, Stanton DE, Carnegie RB, Shields JD, Preu ER (2006) Chytrid infections of Daphnia pulicaria: development, ecology, pathology and phylogeny of Polycaryum laeve. Freshw Biol 51:634–648

    Google Scholar 

  • Jones MDM, Forn I, Gadelha C, Egan MJ, Bass D, Massana R, Richards TA (2011) Discovery of novel intermediate forms redefines the fungal tree of life. Nature 474:200–234

    CAS  PubMed  Google Scholar 

  • Karling JS (1950) The genus Physoderma. Lloydia 13:29–71

    Google Scholar 

  • Karling JS (1965) Catenophlyctis, a new genus of Catenariaceae. Am J Bot 52:133–138

    Google Scholar 

  • Karling JS (1977) Chytridiomycetarum Iconographia. Lubrecht and Cramer, Monticello, NY

    Google Scholar 

  • Kirk PM, Cannon PF, Minter DW, Stalpers JA (2008) Dictionary of the Fungi, 10th edn. CABI Publishing, The Netherlands

    Google Scholar 

  • Kniep H (1930) Über den Generationswechsel von Allomyces. Zeitschrift für Botanik 22:433–441

    Google Scholar 

  • Koch WJ (1956) Studies of the motile cells of chytrids. I. Electron microscope observations of the flagellum, blepharoplast and rhizoplast. Am J Bot 43:811–819

    Google Scholar 

  • Lang BF, O’Kelly C, Nerad T, Gray MW, Burger G (2002) The closest unicellular relatives of animals. Curr Biol 12:1773–1778

    CAS  PubMed  Google Scholar 

  • Lang BF, Laforest M-J, Burger G (2007) Mitochondrial introns: a critical view. Trends Genet 23:119–125

    CAS  PubMed  Google Scholar 

  • Lange L, Olson LW (1979) Uniflagellate phycomycete zoospore. Dansk Botanisk Arkiv 33:7–95

    Google Scholar 

  • Lange L, Olson LW (1980) Transfer of the Physodermataceae from the Chytridiales to the Blastocladiales. Trans Br Mycol Soc 74:449–457

    Google Scholar 

  • Lefèvre E, Bardot C, Noel C, Carrias JF, Viscogliosi E, Amblard C, Sime-Ngando T (2007) Unveiling fungal zooflagellates as members of freshwater picoeukaryotes: evidence from a molecular diversity study in a deep meromictic lake. Environ Microbiol 9:61–71

    PubMed  Google Scholar 

  • Lessie PE, Lovett JS (1968) Ultrastructural changes during sporangium formation and zoospore differentiation in Blastocladiella emersonii. Am J Bot 55:220–236

    CAS  PubMed  Google Scholar 

  • Letcher PM, Powell MJ, Churchill PF, Chambers JG (2006) Ultrastructural and molecular phylogenetic delineation of a new order, the Rhizophydiales (Chytridiomycota). Mycol Res 110:898–915

    CAS  PubMed  Google Scholar 

  • Letcher PM, Velez CG, Barrantes ME, Powell MJ, Churchill PF, Wakefield WS (2008) Ultrastructural and molecular analyses of Rhizophydiales (Chytridiomycota) isolates from North America and Argentina. Mycol Res 112:759–782

    PubMed  Google Scholar 

  • Lingle WL, Barstow WE (1983) Ultrastructure of the zoospore of Blastocladia ramosa (Blastocladiales). Can J Bot 61:3502–3513

    Google Scholar 

  • Liu YJ, Hodson MC, Hall BD (2006) Loss of the flagellum happened only once in the fungal lineage: phylogenetic structure of Kingdom Fungi inferred from RNA polymerase II subunit genes. BMC Evol Biol 6:13

    Google Scholar 

  • Liu Y, Steenkamp ET, Brinkmann H, Forget L, Philippe H, Lang BF (2009) Phylogenomic analyses predict sistergroup relationship of nucleariids and Fungi and paraphyly of zygomycetes with significant support. BMC Evol Biol 9:11

    Google Scholar 

  • Lovett JS (1975) Growth and differentiation of water mold Blastocladiella emersonii – cytodifferentiation and role of ribonucleic acid and protein synthesis. Bacteriol Rev 39:345–404

    CAS  PubMed Central  PubMed  Google Scholar 

  • Lucarotti CJ (1987) Coelomomyces stegomyiae infection in adult Aedes aegypti. Mycologia 79:362–369

    Google Scholar 

  • Lucarotti CJ, Federici BA (1984) Ultrastructure of the gametes of Coelomomyces dodgei Couch (Blastocladiales, Chytridiomycetes). Protoplasma 121:77–86

    Google Scholar 

  • Machlis L (1958a) A study of sirenin, the chemotactic sexual hormone from the watermold Allomyces. Physiol Plant 11:845–854

    CAS  Google Scholar 

  • Machlis L (1958b) Evidence for a sexual hormone in Allomyces. Physiol Plant 11:181–192

    CAS  Google Scholar 

  • Machlis L (1968) Response of male gametes of Allomyces to sexual hormone sirenin. Plant Physiol 43:1319–1320

    CAS  PubMed Central  PubMed  Google Scholar 

  • Machlis L (1969) Zoospore chemotaxis in the water mold Allomyces. Physiol Plant 22:126–139

    CAS  Google Scholar 

  • Madelin MF, Beckett A (1972) Production of planonts by thin-walled sporangia of fungus Coelomomyces indicus – parasite of mosquitos. J Gen Microbiol 72:185–200

    Google Scholar 

  • Manier JF, Loubes C (1978) Callimastix cyclopis Weissenberg, 1912 (Phycomycetes, Blastocladiales) a parasite of Microcyclops claus, 1893 (Copepoda, Cyclopoida) from Tchad - ultrastructural features. Protistologica 14:493–501

    Google Scholar 

  • Manton I, Clarke B, Greenwood AD, Flint EA (1952) Further observations on the structure of plant cilia by combination of visual and electron microscopy. J Exp Bot 3:204–215

    Google Scholar 

  • Martin WW (1970) A morphological and cytological study of Coelomomyces punctatus. M.Sc., University of North Carolina, Chapel Hill

    Google Scholar 

  • Martin WW (1971) The ultrastructure of Coelomomyces punctatus zoospores. J Elisha Mitchell Sci Soc 87:209–221

    Google Scholar 

  • Martin WW (1975) A new species of Catenaria parasitic in midge eggs. Mycologia 67:264–272

    CAS  PubMed  Google Scholar 

  • Martin WW (1978) Two additional species of Catenaria (Chytridiomycetes, Blastocladiales) parasitic in midge eggs. Mycologia 70:461–467

    Google Scholar 

  • Martin WW (1987) Zoosporic parasites of aquatic insects: collection, identification, and culture. In: Fuller MS, Jaworski A (eds) Zoosporic fungi in teaching and research. Southeastern, Athens, GA, pp 137–142

    Google Scholar 

  • Massey SE, Garey JR (2007) A comparative genomics analysis of codon reassignments reveals a link with mitochondrial proteome size and a mechanism of genetic code change via suppressor tRNAs. J Mol Evol 64:399–410

    CAS  PubMed  Google Scholar 

  • Matthews VD (1937) A new genus of the Blastocladiaceae. J Elisha Mitchell Sci Soc 53:191–195

    Google Scholar 

  • McCrainie J (1942) Sexuality in Allomyces cystogenus. Mycologia 34:209–213

    Google Scholar 

  • Mills GL, Cantino EC (1979) Trimodal formation of microbodies and associated biochemical and cytochemical changes during development in Blastocladiella emersonii. Exp Mycol 3:53–69

    CAS  Google Scholar 

  • Mills GL, Cantino EC (1981) Chitosome-like vesicles from gamma-particles of Blastocladiella emersonii synthesize chitin. Arch Microbiol 130:72–77

    CAS  Google Scholar 

  • Mitchell RT, Deacon JW (1986) Selective accumulation of zoospores of chytridiomycetes and oomycetes on cellulose and chitin. Trans Br Mycol Soc 86:219–223

    Google Scholar 

  • Nagahama T, Sato H, Shimazu M, Sugiyama J (1995) Phylogenetic divergence of the entomophthoralean fungi: evidence from nuclear 18S ribosomal RNA gene sequences. Mycologia 87:203–209

    CAS  Google Scholar 

  • Nascimento CDA, Pires-Zottarelli CLA (2010) Blastocladiales e Spizellomycetales do Parque Estadual da Serra da Cantareira, São Paulo, Brasil. Revista Brasileira de Botânica 33:693–704

    Google Scholar 

  • Nolan RA (1969) Nutritional requirements for species of Allomyces. Mycologia 61:641–644

    CAS  PubMed  Google Scholar 

  • Nolan RA (1970) Sulfur source and vitamin requirements of aquatic phycomycete, Catenaria anguillulae. Mycologia 62:568–577

    CAS  Google Scholar 

  • Nolan RA (1985) Physiology and biochemistry. In: Couch JN, Bland CE (eds) The genus Coelomomyces. Academic, Orlando, FL, pp 321–348

    Google Scholar 

  • Olson LW (1974) Meiosis in the aquatic Phycomycete Allomyces macrogynus. Comptes rendus des travaux du laboratoire Carlsberg 40:113–124

    Google Scholar 

  • Olson LW (1980) Allomyces neo-moniliformis gametogenesis. The Cystogenes life cycle. Protoplasma 105:87–106

    Google Scholar 

  • Olson LW (1984) Allomyces – a different fungus. Opera Bot 73:5–96

    Google Scholar 

  • Olson LW, Borkhardt B (1978) Polyploidy and its control in Allomyces macrogynus. Trans Br Mycol Soc 71:65–76

    Google Scholar 

  • Olson LW, Lange L (1978) Meiospore of Physoderma maydis – causal agent of physoderma disease of maize. Protoplasma 97:275–290

    Google Scholar 

  • Olson LW, Lange L (1983) The gamma body- a vesicle generating structure. Nord J Bot 3:673–680

    Google Scholar 

  • Olson LW, Reichle R (1978a) Meiosis and diploidization in the aquatic Phycomycete Catenaria anguillulae. Trans Br Mycol Soc 70:423–437

    Google Scholar 

  • Olson LW, Reichle R (1978b) Synaptonemal complex formation and meiosis in the resting sporangium of Blastocladiella emersonii. Protoplasma 97:261–273

    Google Scholar 

  • Olson LW, Lange L, Reichle R (1978) Zoospore and meiospore of aquatic phycomycete Catenaria anguillulae. Protoplasma 94:53–71

    Google Scholar 

  • Paquin B, Lang BF (1996) The mitochondrial DNA of Allomyces macrogynus: the complete genomic sequence from an ancestral fungus. J Mol Biol 255:688–701

    CAS  PubMed  Google Scholar 

  • Paquin B, Laforest MJ, Forget L, Roewer I, Wang Z, Longcore J, Lang BF (1997) The fungal mitochondrial genome project: evolution of fungal mitochondrial genomes and their gene expression. Curr Genet 31:380–395

    CAS  PubMed  Google Scholar 

  • Petersen HE (1909) Studier over Ferskvands-Phycomyceter. Bidrag til Kundskaben om de submerse Phykomyceters Biologi og Systematik, samt om deres Udbredelse i Danmark. Bot Tidskrift 29:345–440

    Google Scholar 

  • Picard KT, Letcher PM, Powell MJ (2009) Rhizidium phycophilum, a new species in Chytridiales. Mycologia 101:696–706

    PubMed  Google Scholar 

  • Pommerville J (1977) Chemotaxis of Allomyces gametes. Exp Cell Res 109:43–51

    CAS  PubMed  Google Scholar 

  • Pommerville J (1978) Analysis of gamete and zygote motility in Allomyces. Exp Cell Res 113:161–172

    CAS  PubMed  Google Scholar 

  • Porter TM, Martin WM, James TY, Longcore JE, Gleason F, Adler PH, Letcher PM, Vilgalys R (2011) Molecular phylogeny of the Blastocladiomycota (Fungi) based on nuclear ribosomal data. Fungal Biol 115:381–392

    CAS  PubMed  Google Scholar 

  • Powell MJ (1978) Phylogenetic implications of microbody-lipid globule complex in zoosporic fungi. BioSyst 10:167–180

    CAS  Google Scholar 

  • Powell MJ (1983) Localization of antimonate-mediated precipitates of cations in zoospores of Chytriomyces hyalinus. Exp Mycol 7:266–277

    CAS  Google Scholar 

  • Powell MJ, Koch WJ (1977a) Morphological variations in a new species of Entophlyctis. I. Species concept. Can J Bot 55:1668–1685

    Google Scholar 

  • Powell MJ, Koch WJ (1977b) Morphological variations in a new species of Entophlyctis. II. Influence of growth-conditions on morphology. Can J Bot 55:1686–1695

    Google Scholar 

  • Pritchard AE, Seilhammer JJ, Mahalingam R, Sable CL, Venuti SE, Cummings DJ (1990) Nucleotide sequence of the mitochondrial genome of Paramecium. Nucleic Acids Res 18:173–180

    CAS  PubMed Central  PubMed  Google Scholar 

  • Reichle RE, Fuller MS (1967) Fine structure of Blastocladiella emersonii zoospores. Am J Bot 54:81–92

    Google Scholar 

  • Remy W, Taylor TN, Hass H (1994) Early Devonian fungi – a Blastocladalean fungus with sexual reproduction. Am J Bot 81:690–702

    Google Scholar 

  • Ribichich KF, Salem-Izacc SM, Georg RC, Vencio RZN, Navarro LD, Gomes SL (2005) Gene discovery and expression profile analysis through sequencing of expressed sequence tags from different developmental stages of the chytridiomycete Blastocladiella emersonii. Eukaryot Cell 4:455–464

    PubMed Central  PubMed  Google Scholar 

  • Robertson JA (1972) Phototaxis in a new Allomyces. Arch f Mikrobiol 85:259–266

    CAS  Google Scholar 

  • Ruiz-Trillo I, Burger G, Holland PWH, King N, Lang BF, Roger AJ, Gray MW (2007) The origins of multicellularity: a multi-taxon genome initiative. Trends Genet 23:113–118

    CAS  PubMed  Google Scholar 

  • Schadt CW, Martin AP, Lipson DA, Schmidt SK (2003) Seasonal dynamics of previously unknown fungal lineages in tundra soils. Science 301:1359–1361

    CAS  PubMed  Google Scholar 

  • Schardl CL, Craven KD (2003) Interspecific hybridization in plant-associated fungi and oomycetes: a review. Mol Ecol 12:2861–2873

    CAS  PubMed  Google Scholar 

  • Scherffel A (1925) Endophytische Phycomyceten-Parasiten der Bacillariaceen und einege neue Monadinen. Ein Beitrag zur Phylogenie der Oomyceten (Schröter). Archiv Protistenk 52:1–141

    Google Scholar 

  • Schroeter J (1893) Phycomycetes. Natürlichen Pflanzenfam 1:63–141

    Google Scholar 

  • Seif E, Leigh J, Liu Y, Roewer I, Forget L, Lang BF (2005) Comparative mitochondrial genomics in zygomycetes: bacteria-like RNase P RNAs, mobile elements and a close source of the group I intron invasion in angiosperms. Nucleic Acids Res 33:734–744

    CAS  PubMed Central  PubMed  Google Scholar 

  • Shaw DS, Cantino EC (1969) An albino mutant of Blastocladiella emersonii - comparative studies of zoospore behaviour and fine structure. J Gen Microbiol 59:369–382

    Google Scholar 

  • Simmons DR, James TY, Meyer AF, Longcore JE (2009) Lobulomycetales, a new order in the Chytridiomycota. Mycol Res 113:450–460

    CAS  PubMed  Google Scholar 

  • Singh KP, Jaiswal RK, Kumar N (2007) Catenaria anguillulae Sorokin: a natural biocontrol agent of Meloidogyne graminicola causing root knot disease of rice (Oryza sativa L.). World J Microbiol Biotechnol 23:291–294

    Google Scholar 

  • Slapeta J, Moreira D, Lopez-Garcia P (2005) The extent of protist diversity: insights from molecular ecology of freshwater eukaryotes. Proc R Soc B Biol Sci 272:2073–2081

    CAS  Google Scholar 

  • Sparrow FK (1939) The entomogenous chytrid Myrophagus Thaxter. Mycologia 304:113–116

    Google Scholar 

  • Sparrow FK (1960) Aquatic phycomycetes. University of Michigan Press, Ann Arbor, MI

    Google Scholar 

  • Sparrow FK (1962) Urophlyctis and Physoderma. Trans Mycol Soc Jpn 3:16–18

    Google Scholar 

  • Sparrow FK (1965) Concerning Physoderma graminis. Mycologia 57:624–627

    Google Scholar 

  • Sparrow FK, Griffin JE (1964) Observation on chytridiaceous parasites of phanerograms. XV. Host range and species concepts studies in Physoderma. Arch f Mikrobiol 40:275–282

    Google Scholar 

  • Stumm C, Hermans JMH, Croes AF, Bucks JH (1976) Chemotaxis and transport of amino acids in Allomyces arbuscula. Ant v Leeuwenhoek 42:203–209

    CAS  Google Scholar 

  • Tabak HH, Cooke WB (1968) Effects of gaseous environments on growth and metabolism of fungi. Bot Rev 34:126–252

    CAS  Google Scholar 

  • Tambor JHM, Ribichich KF, Gomes SL (2008) The mitochondrial view of Blastocladiella emersonii. Gene 424:33–39

    CAS  PubMed  Google Scholar 

  • Tanabe Y, O’Donnell K, Saikawa M, Sugiyama J (2000) Molecular phylogeny of parasitic Zygomycota (Dimargaritales, Zoopagales) based on nuclear small subunit ribosomal DNA sequences. Mol Phylogenet Evol 16:253–262

    CAS  PubMed  Google Scholar 

  • Tanabe Y, Watanabe MM, Sugiyama J (2002) Are Microsporidia really related to Fungi?: a reappraisal based on additional gene sequences from basal fungi. Mycol Res 106:1380–1391

    CAS  Google Scholar 

  • Tanabe Y, Saikawa M, Watanabe MM, Sugiyama J (2004) Molecular phylogeny of Zygomycota based on EF-1 and RPB1 sequences: limitations and utility of alternative markers to rDNA. Mol Phylogenet Evol 30:438–449

    CAS  PubMed  Google Scholar 

  • Tanabe Y, Watanabe MM, Sugiyama J (2005) Evolutionary relationships among basal fungi (Chytridiomycota and Zygomycota): insights from molecular phylogenetics. J Gen Appl Microbiol 51:267–276

    CAS  PubMed  Google Scholar 

  • Taylor JW, Fuller MS (1981) The Golgi apparatus, zoosporogenesis, and development of the zoospore discharge apparatus of Chytridium confervae. Exp Mycol 5:35–59

    Google Scholar 

  • Taylor TN, Remy W, Hass H (1994) Allomyces in the Devonian. Nature 367:601–601

    Google Scholar 

  • Taylor JW, Jacobson DJ, Kroken S, Kasuga T, Geiser DM, Hibbett DS, Fisher MC (2000) Phylogenetic species recognition and species concepts in fungi. Fungal Genet Biol 31:21–32

    CAS  PubMed  Google Scholar 

  • Teter HE (1944) Isogamous sexuality in a new strain of Allomyces. Mycologia 36:194–210

    Google Scholar 

  • Travland LB (1979) Structures of the motile cells of Coelomomyces psorophorae and function of the zygote in encystment on a host. Can J Bot 57:1021–1035

    Google Scholar 

  • Vandenkoornhuyse P, Baldauf SL, Leyval C, Straczek J, Young JPW (2002) Evolution - Extensive fungal diversity in plant roots. Science 295:2051–2051

    PubMed  Google Scholar 

  • Vavra J, Joyon L (1966) Etude sur la morphologie le cycle evolutif et la position systematique de Callimastix cyclopis Weissenberg. Protistologica 2:5–15

    Google Scholar 

  • Whisler HC (1987) On the isolation and culture of water molds: the Blastocladiales and Monoblepharidales. In: Fuller MS, Jaworski A (eds) Zoosporic fungi in teaching and research. Southeastern, Athens, GA, pp 121–124

    Google Scholar 

  • Willoughby LG (1959) A new species of Blastocladiella from Great Britain. Trans Br Mycol Soc 42:287–291

    Google Scholar 

  • Wilson CM (1952) Meiosis in Allomyces. Bull Torr Bot Club 79:139–160

    Google Scholar 

  • Wilson CM, Flanagan PW (1968) The life cycle and cytology of Brachyallomyces. Can J Bot 46:1361–1367

    Google Scholar 

  • Wolf FT (1941) A contribution to the life history and geographic distribution of the genus Allomyces. Mycologia 33:158–173

    Google Scholar 

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James, T.Y., Porter, T.M., Martin, W.W. (2014). 7 Blastocladiomycota. In: McLaughlin, D., Spatafora, J. (eds) Systematics and Evolution. The Mycota, vol 7A. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-55318-9_7

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