Trois Especes Nouvelles d'Ophryoglenes: O. gelifera n. sp., O. mucosa n. sp., O. multimicronucleata n. sp. (Cilies Holotriches Peniculiens)

SYNOPSIS. A previous study with P. de Puytorac on O. bacterocaryon(3) has shown the methods of studying this Ciliate and has specified the general and buccal morphology, the morphogenesis, and the biology of vegetative individuals (theront, trophont, tomont, tomites) of this species. Three species we are describing now offer numerous common features with O. bacterocaryon. We consider them as the proper characters of genus Ophryoglena and we only insist on the specific particularities of O. gelifera, O. mucosa and O. multimicronucleata. O. gelifera is a large Ophryoglene differing from the others by a slightly asymetric, curved, spindle-shaped theront; the ellipsoidal tomont secretes abundant and clear jelly. The theront possesses one thick spindle-shaped macronucleus, one voluminous spherical micronucleus, fitting with the macronucleus. Its somatic infraciliature is dense, its buccal infraciliature is characteristic, especially in the shape of peniculus P1. This species cannot be mistaken for O. pectans Mugard(2) although it is rather near it. O. mucosa is a very small Ophryoglene. The theront has one thick elliptical macronucleus, one small micronucleus; the buccal orifice is not kidney-shaped, but quite pointed in front; there is no tragus; the somatic infraciliature is not close; the peniculus P1 is characteristic. The tomont is ellipsoidal and surrounded by a thick mucous gangue. The tomites are not close together. O. mucosa is very different from O. gelifera and O. pectans Mugard(2). O. multimicronucleata. Near to O. polymicrocaryon Mugard(2), this Ophryoglene differs from it by the small size of all its vegetative elements and especially by its nuclear-apparatus. The latter includes numerous (5 to 6) bulky spherical micronuclei and one macronucleus looking like blackpudding which can be compared to that of O. singularis Canella and Trinchas(1). The theront is spindle-shaped and of a dark-grey colour. The spherical tomont secretes a mucous gangue which is not very thick. Besides, the somatic infraciliature and buccal in fraciliature of the theront (peniculus P1 especially) make O. multi micronucleata quite distinct from O. polymicrocaryon Mugard(2).     

Erhardorina n. g., Ascogregarina polynesiensis n. sp., Eimeria golemanskii n. sp., Isospora tamariscini n. sp., Gregarina kazumii n. nom., new combinations and emendations in the names of apicomplexan protozoa

On the basis of a review of the approximately 4300 species of apicomplexan protozoa, the following new species, new names, new combinations, and emendations are given: NEW GENUS, Erhardovina; NEW SPECIES, Ascogregarina polynesiensis, Eimeria golemanskii, Isospora tamariscini; NEW NAME, Gregarina kazumii; NEW COMBINATIONS, Ascogregarina brachyceri (Purrini, 1980), Erhardovina euzeti (Lipa, 1981), E. scutovertexi (Erhardová, 1955), Haemorhormidium batrachi (Chaudhuri & Choudhury, 1983); EMENDATIONS, Selenidium francianum (Arvy, 1952) Tuzet & Ormières, 1965, Pyxinioides bolitoides D. P. Henry, 1938, P. japonicus H. Hoshide, 1951, P. kamenote H. Hoshide, 1951, P. kurofuji H. Hoshide, 1951, P. oshoroensis H. Hoshide, 1951, P. pugetensis D. P. Henry, 1938, Gregarina levinei Haldar & Sarkar, 1980, Retractocephalus halticae Haldar, Chakraborty & Kundu, 1982, Cnemidospora schizophylli Tuzet & Guerin, 1947, Grebneckiella indica (Merton, 1911) Watson, 1916, Quadruspinospora atractomorphae Haldar & Chakraborty, 1978, Haemogregarina acipenseri Nawrotzky, 1914, H. lobianci Yakimov & Kohl-Yakimov, 1912, H. yakimovikohlae Wladimiroff, 1910, Hepatozoon luehi (Sambon, 1909) Pessoa, Cavalheiro & de Souza, 1970, Eimeria beyerae Ovezmukhammedov, 1977, E. (?) gigantea (Labbé, 1896) Reichenow, 1921, E. (?) labbei Hardcastle, 1943, E. rufi Prasad, 1960, E. (?) scylii (Drago, 1902) Levine & Becker, 1933, Isospora corvi Ray, Shivnani, Oommen & Bhaskaran, 1952, I. melopsittaci Bhatia, Chauhan, Arora & Agrawal, 1973, I. seicerci Ray, Shivnani, Oommen & Bhaskaran, 1952, I. stomatici Chakravarty & Kar, 1944, I. triffitae Nukerbaeva & Svanbaev, 1973, Wenyonella mackinnonae Misra, 1947, Octosporella sanguinolentae Ovezmukhammedov, 1975, Lankesterella millani Alvarez Calvo, 1975, Sarcocystis woodhousei Dogel', 1916, Haemoproteus lari Yakunin, 1972, Babesia ninakohlyakimovae (Yakimoff & Shokhor, 1916), Theileria ninakohlyakimovae (Yakimov, 1916) Krylov, 1974, Haemohormidium batrachi (Chaudhuri & Choudhury, 1983).     

Erhardorina n. g., Ascogregarina polynesiensis n. sp., Eimeria golemanskii n. sp., Isospora tamariscini n. sp., Gregarina kazumii n. nom., New Combinations and Emendations in the Names of Apicomplexan Protozoa1

On the basis of a review of the approximately 4300 species of apicomplexan protozoa, the following new species, new names, new combinations, and emendations are given: NEW GENUS,Erhardovina; NEW SPECIES,Ascogregarina polynesiensis, Eimeria golemanskii, Isospora tamariscini; NEW NAME,Gregarina kazumii; NEW COMBINATIONS,Ascogregarina brachyceri (Purrini, 1980),Erhardovina euzeti (Lipa, 1981),E. scutovertexi (Erhardová, 1955),Haemorhormidium batrachi (Chaudhuri & Choudhury, 1983); EMENDATIONS,Selenidium francianum(Arvy, 1952) Tuzet & Ormières, 1965,Pyxinioides bolitoides D. P. Henry, 1938,P. japonicus H. Hoshide, 1951,P. kamenote H. Hoshide, 1951,P. kurofuji H. Hoshide, 1951,P. oshoroensis H. Hoshide, 1951,P. pugetensis D. P. Henry, 1938, Gregarina levinei Haldar & Sarkar, 1980,Retractocephalus halticae Haldar, Chakraborty & Kundu, 1982,Cnemidospora schizophylli Tuzet & Guerin, 1947,Grebneckiella indica (Merton, 1911) Watson, 1916,Quadruspinospora atractomorphae Haldar & Chakraborty, 1978,Haemogregarina acipenseri Nawrotzky, 1914,H. lobianci Yakimov & Kohl-Yakimov, 1912,H. yakimovikohlae Wladimiroff, 1910,Hepatozoon luehi (Sambon, 1909) Pessoa, Cavalheiro & de Souza, 1970,Eimeria beyerae Ovezmukhammedov, 1977, E. (?) gigantea (Labbé, 1896) Reichenow, 1921, E. (?) labbei Hardcastle, 1943, E. rufi Prasad, 1960, E. (?) scylii (Drago, 1902) Levine & Becker, 1933, Isospora corvi Ray, Shivnani, Oommen & Bhaskaran, 1952,I. melopsittaci Bhatia, Chauhan, Arora & Agrawal, 1973, I. seicerci Ray, Shivnani, Oommen & Bhaskaran, 1952,I. stomatici Chakravarty & Kar, 1944,I. triffitae Nukerbaeva & Svanbaev, 1973,Wenyonella mackinnonae Misra, 1947,Octosporetla sanguinolentae Ovezmukhammedov, 1975,Lankesterella millani Alvarez Calvo, 1975,Sarcocystis woodhousei Dogel', 1916,Haemoproteus lari Yakunin, 1972, Babesia ninakohlyakimovae (Yakimoff & Shokhor, 1916),Theileria ninakohlyakimovae (Yakimov, 1916) Krylov, 1974,Haemohormidium batrachi(Chaudhuri & Choudhury, 1983).     

Oenothorachona ectenolaemus n.g., n.sp. and Spirochona halophila n.sp., Two New Marine Chonotrichous Ciliates

SYNOPSIS. Two new species of chonotrichous ciliates, Oenophorachona ectenolaemus n.g., n.sp. and Spirochona halophila n.sp. were found on Anisogammarus sp. collected from the waters of Humboldt County, California and Argyle Bay, San Juan Island, Washington. This is the 1st reported occurrence of 2 genera of chonotrichous ciliates on a single host species as well as the 1st of the occurrence of Spirochona in marine and brackish water environments.     

Rhizochrysidopsis vorax,n. gen., n. sp.

Zusammenfassung Die Art ist durch eine bedeutende Variation der Zellgröße, damit auch des Chromatophors und des Kerns ausgezeichnet. Mit steigender Zellgröße nimmt die Zahl der kontraktilen Vakuolen von zwei auf mindestens acht zu. — Unter Umständen erfolgt exzessive animalische Ernährung; es werden auch im Vergleich zum Zellkörper sehr große Algenzellen aufgenommen und verdaut.     

Actiniscus canadensis n. sp., A. pentasterias Ehrenberg v. arcticus n. var., Pseudoactiniscus apentasterias n. gen., n. sp., Marine Relicts in Canadian Arctic Lakes

SYNOPSIS. The family Actiniscaceae Kützing, 1845, (generally placed in the dinoflagellates) includes species derived from Actiniscus pentasterias Schütt, some of which became lacustrine relicts. A. pentasterias v. arcticus. living in Arctic and Altantic waters, differs from the Mediterranean species in having a greater number of siliceous skeletons (pentasters). Advanced atrophy of pentasters in lacustrine A. canadensis , and absence of such structures in Pseudoactiniscus apentasterias , probably results from decreased salinity and an undetermined ecologic factor. Morphogenesis and physiologic transformation of past euryhaline Actiniscaceae into contemporary limnobionts began, presumably, during the prelimnic phase of Great Bear Lake and Keyhole Lake. Arctic Actiniscus which exist under subzero temperatures and endure 10-month-long winters, appear to satisfy their energy requirements by heterotrophy and frequent phagocytosis. Survival of lacustrine Actiniscus species in both Arctic lakes seems possible because of lack of competition from co-existing phytoplankton organisms which can endure extreme dystrophic conditions.     

Einige Chrysophyceen (Ochromonas minuta n. sp., Synochromonas korschikoffii n. sp., Monas spec.)

Zusammenfassung Es wurde versucht, durch Ernährungsversuche mit Reinkulturen von verschiedenen Chrysophyceen einen besseren Einblick in die Bedürfnisse der Angehörigen dieser Klasse zu erzielen.Zucker hat sich bei den untersuchten Arten überall als notwendig für gutes Wachstum erwiesen, bei gefärbten wie bei farblosen Arten. Ochromonas minuta n. sp. hat gut gefärbte Chromatophoren und einen Augenfleck, ist aber O. malhamensis in ihrer Photosynthese nur wenig überlegen. Ohne Bakterien und organische Abkochungen wurde Vermehrung nur erreicht, wenn die Vitamine B₁ und B₁₂ sowie B₆ (Pyridoxin) zugegeben wurden. Synochromonas korschikoffii n. sp. hat Kugelkolonien, deren Bau und Vermehrung geschildert wird. Außer B₁ und B₁₂ erwies sich auch Erdabkochung als unentbehrlich.Mehrere Monas-Stämme wurden kultiviert, 4 davon in Reinkultur. Auch Monas scheint allgemein B₁ und B₁₂ zu brauchen. Animalische Ernährung ist nicht Bedingung für Vermehrung. Ochromonas und Monas wachsen auch auf Agar, wenn er feucht genug ist. Alle geprüften Chrysophyceen können sich im Dunkeln vermehren.Uniterstützt durch die Deutsche Forschungsgemeinschaft.     

Parauronema virginianum n. g., n. sp., a Marine Hymenostome Ciliate

SYNOPSIS. Parauronema virginianum n. g., n. sp., a marine hymenostome ciliate is described from the Virginia coast. Structural studies were made on specimens treated with the Chatton-Lwoff silver impregnation technic and on animals observed with the phase microscope. Particular attention was given to the buccal ciliature and its importance to generic assignment in the order Hymenostomatida.     

Platyamoeba stenopodia. n. g., n. sp., a Freshwater Amoeba*

SYNOPSIS. Platyamoeba stenopodia n. g., n. sp., isolated from a lake in Alabama, is an amoeba with flattened form, usually more than 2.5 × as long as broad, the anterior half hyaline and the posterior half granular, with a single vesiculate nucleus at the posterior edge of the hyaline region. It forms a transitory floating stage with slender, hyaline pseudopods. Its cyst is spherical, uninucleate, with a smooth inner wall and a thinner, closely applied outer wall, which is often slightly wrinkled. Length of locomotive amoeba 15–36 μ diameter of cyst 7–11.5 μ Reproduction by binary fission with mesomitotic nuclear division, the nuclear membrane disappearing in prophase. The genus Platyamoeba is erected for amoebae including this organism; the type species is P. placida.     

Eimeria clethrionomysis sp. n., Eimeria gallatii sp. n., Eimeria pileata sp. n. and Eimeria marconii sp. n. from the red-backed vole Clethrionomys gapperi Vigors, from Pennsylvania.

Four new eimerian species are described from red-backed voles, Clethrionomys gapperi in Pennsylvania. Sporulated oocysts of Eimeria clethrionomyis sp. n. are ellipsoidal, 18.8 (16.5-21.5) x 14.9 (14.0-16.5) with elongate, ovoid sporocysts, 10.6 (9.5-12.0) x6.1 (5.5-7.0). The oocyst wall is smooth, with 2 layers, and thins, with terminal cap at one or both ends. Polar granules, dark Stieda body and sporocyst residuum are present. The oocyst residuum is absent. Sporulated oocysts of Eimeria gallatii sp. n. are ellipsoidal, 27.7 (21-32) x 19.3 (17-24) with ovoid sporocysts, 13.5 (12-15) x 8.8 (8-10). The oocyst wall is smooth, 2-layered, with a micropyle and thin wall at the end opposite the micropyle. Polar granules, Stieda body and sporocyst residuum are present. The oocyst residuum is atypical, of cobwebby material. Sporulated oocysts of Eimeria pileata sp. n. are subspherical to spherical, 25.2 (20.5-29.5) x 22.5 (19.5-25.5) with ellipsoidal sporocysts, 13.4(10.5-15.0) x 8.4 (7.5-9.5). The oocyst wall is rough, pitted, striated, 2-layered, with no micropyle. Polar granules, oocyst and sporocyst residuum, Stieda body and stiedal cap are present. Sporulated oocysts of Eimeria marconii sp. n. are ellipsoidal, 13.0 (10.5-15-0) x 10.6 (9.5-12.0) with elongate, ovoid sporocysts, 7.7 (7.0-8.5) x 4.2 (3.0-4.5). The oocyst wall is smooth, single-layered, with no micropyle. Polar granules, dark Stiedal body and sporocyst residuum are present. There is no oocyst residuum.     

Cthulhu Macrofasciculumque n. g., n. sp. and Cthylla Microfasciculumque n. g., n. sp., a Newly Identified Lineage of Parabasalian Termite Symbionts

The parabasalian symbionts of lower termite hindgut communities are well-known for their large size and structural complexity. The most complex forms evolved multiple times independently from smaller and simpler flagellates, but we know little of the diversity of these small flagellates or their phylogenetic relationships to more complex lineages. To understand the true diversity of Parabasalia and how their unique cellular complexity arose, more data from smaller and simpler flagellates are needed. Here, we describe two new genera of small-to-intermediate size and complexity, represented by the type species Cthulhu macrofasciculumque and Cthylla microfasciculumque from Prorhinotermes simplex and Reticulitermes virginicus, respectively (both hosts confirmed by DNA barcoding). Both genera have a single anterior nucleus embeded in a robust protruding axostyle, and an anterior bundle flagella (and likely a single posterior flagellum) that emerge slightly subanteriorly and have a distinctive beat pattern. Cthulhu is relatively large and has a distinctive bundle of over 20 flagella whereas Cthylla is smaller, has only 5 anterior flagella and closely resembles several other parababsalian genera. Molecular phylogenies based on small subunit ribosomal RNA (SSU rRNA) show both genera are related to previously unidentified environmental sequences from other termites (possibly from members of the Tricercomitidae), which all branch as sisters to the Hexamastigitae. Altogether, Cthulhu likely represents another independent origin of relatively high cellular complexity within parabasalia, and points to the need for molecular characterization of other key taxa, such as Tricercomitus.     

Eimeria clethrionomyis sp. n., Eimeria gallatii sp. n., Eimeria pileata sp. n. and Eimeria marconii sp. n. from the Red-Backed Vole Clethrionomys gapperi Vigors,from Pennsylvania§

SYNOPSIS Four new eimerian species are described from red-backed voles. Clethrionomys gapperi in Pennsylvania. Sporulated oocysts of Eimeria clethrionomyis sp. n. are ellipsoidal, 18.8 (16.5–21.5) × 14.9 (14.0–16.5) with elongate, ovoid sporocysts, 10.6 (9.5–12.0) × 6.1 (5.5–7.0). The oocyst wall is smooth, with 2 layers, and thins, with terminal cap at one or both ends. Polar granules, dark Stieda body and sporocyst residuum are present. The occyst residuum is absent. Sporulated oocysts of Eimeria gallatii sp. n. are ellipsoidal, 27.7 (21–32) × 19.3 (17–24) with ovoid sporocysts, 13.5 (12–15) × 8.8 (8–10). The oocyst wall is smooth, 2-layered, with a micropyle and thin wall at the end opposite the micropyle. Polar granules. Stieda body and sporocyst residuum are present. The oocyst residuum is atypical, of cobwebby material. Sporulated oocysts of Eimeria pileata sp. n. are subspherical to spherical, 25.2 (20.5–29.5) × 22.5(19.5–25.5) with ellipsoidal sporocysts, 13.4(10.5–15.0) × 8.4 (7.5–9.5). The oocyst wall is rough, pitted, striated, 2-layered, with no micropyle. Polar granules, oocyst and sporocyst residuum. Stieda body and stiedal cap are present. Sporulated oocysts of Eimeria marconii sp. n. are ellipsoidal, 13.0 (10.5–15.0) × 10.6 (9.5–12.0) with elongate, ovoid sporocysts, 7.7 (7.0–8.5) × 4.2 (3.0–4.5). The oocyst wall is smooth, single-layered, with no micropyle. Polar granules, dark Stieda body and sporocyst residuum are present. There is no oocyst residuum.     

Two amphistomes,Lobatodiscus australiensis n.g., n.sp. and Elseyatrema microacetabularis n.g., n.sp., from the Australian turtle Elseya dentata (Gray)

Summary Lobatodiscus australiensis n.g., n.sp. (family and subfamily uncertain) and Elseyatrema microacetabularis n.g., n.sp. (family Paramphistomidae, subfamily Dadaytrematinae?), from the intestine of the freshwater turtle Elseya dentata (Gray) in Queensland, Australia, are described. Lobatodiscus has a large lobed acetabulum, small oral diverticula which do not protrude out of the oral sucker, two pairs of lymph vessels and no oesophageal bulb. Elseyatrema has a small acetabulum, large protruding oral diverticula, an oesophageal bulb, juxtaposed testes, one pair of rudimentary lymph vessels and no cirrus-sac. ac]19830626     

Monopylocystis visvesvarai n. gen., n. sp. and Sawyeria marylandensis n. gen., n. sp.: two new amitochondrial heterolobosean amoebae from anoxic environments

Two new species of heterolobosean amoebae from anoxic environments, Monopylocystis visvesvarai and Sawyeria marylandensis, are described on the basis of light microscopy, electron microscopy, and their phylogenetic affiliation based on analyses of nuclear small-subunit ribosomal RNA gene sequences. Both species lack mitochondria but have organelles provisionally interpreted as hydrogenosomes, and neither can tolerate aerobic conditions. As their conditions of culture do not exclude all oxygen, they may be microaerophiles rather than strict anaerobes. Both species have unusual nucleolar morphologies. Monopylocystis visvesvarai, from a marine sediment, has nucleolar material distributed around the nuclear periphery. It is the first non-aerobic heterolobosean protist for which a cyst is known; the cyst is unmineralized and unornamented except for a single, raised, plugged pore. Sawyeria marylandensis, from an iron-rich freshwater stream, has nucleolar material distributed in one or two parietal masses, which persist during mitosis. In phylogenetic analyses of small-subunit rRNA gene sequences, Monopylocystis visvesvarai, Sawyeria marylandensis and Psalteriomonas lanterna converge to form a single clade of non-aerobic (anaerobic/microaerophilic) heteroloboseans.     

Adelphamoeba galeacystis n. g., n. sp., an Amoeboflagellate Isolated from Soil*

SYNOPSIS. An amoeboflagellate isolated from common soil is described. The amoeboid stage is typically limax and contains a well differentiated uroid region. The flagellate has 2 flagella, which emerge anteriorly and are equal in length. It has a ventral cytostome near the anterior border. The cyst is helmet-shaped and without opercula. Polar masses are present during nuclear division.     

Proleptonchoides southindiae n. gen., n. sp., a New Leptonchoid from South India

Proleptonchoides southindiae n. gen., n. sp. (Dorylaimida: Leptonchidae), is described from soil around false tobacco (Lobelia excelsa) and cardamom (Elettaria cardamomurn) in South India. P. southindiae is prodelphic, has a short constricted esophageal bulb and flanged odontophore, and is phylogenetically close to Proleptonchus.