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.     

Fossil onychophorans from Dominican and Baltic amber: Tertiapatus dominicanus n.g., n.sp. (Tertiapatidae n.fam.) and Succinipatopsis balticus n.g., n.sp. (Succinipatopsidae n.fam.) with a proposed classification of the subphylum Onychophora

Abstract. Tertiapatus dominicanus n.g., n.sp. (Tertiapatidae n.fam.) and Succinipatopsis balticus n.gen., n.sp. (Succinipatopsidae n.fam.) (Lobopodia: Onychophora), the first Tertiary fossils of the Lobopodia, are described from Dominican and Baltic amber, respectively. Both families are characterized by the presence of simple legs lacking foot portions with claws and pads. Tertiapatidae is further characterized by soluble body pigments and oral papillae shorter than the legs. Succinipatopsidae is characterized by non-soluble body pigments and oral papillae longer than the legs. Nomenclatural changes include the erection of the class Udeonychophora n. nom. for terrestrial onychophorans with a ventral mouth, the order Ontonychophora n.nom. for extant onychophorans possessing legs with a differentiated "foot" portion, and the family Helenodoridae n.nom. for the genus Helenodora from the Carboniferous. The biogeographical significance of these fossils and their phylogenetic relationship with previously described onychophorans are discussed.     

Gloeococcus bavaricus n. sp. undCoelastrella compacta n. sp.

Ohne Zusammenfassung     

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).     

Tylenchocriconema alleni n. g., n. sp. from Guatemala (Tylenchocriconematidae n. fam.; Tylenchocriconematidae n. superfam.; Nematoda)

Tylenchocriconema alleni n.g.n.sp, is described from soil about roots of a bromeliad from Guatemala City, Guatemala. It has characteristics of both the Tylenchoidea and Criconematoidea. Tylenchocriconematidae, n. fam., and Tylenchocriconematoidea, n. superfam., are proposed to express the relationship of this species to other taxa. Tylenchulidae and Paratylenchidae are considered closely related, and Tylenchulidoidea, n. rank, is proposed to indicate their relationship.     

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.     

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.     

The subfamily Encotyllabinae (Monogenea: Capsalidae) with the description of Alloencotyllabe caranxi n. g., n. sp. and Encotyllabe kuwaitensis n. sp.

Alloencotyllabe caranxi n. g., n. sp. is found in groups of 9–15 specimens attached close together to the lower pharyngeal plate of Caranx sp. It is characterized by having an elongate body, a prohaptor with large spines, an armed penis which lies in a pouch and a vaginal pouch guarded by two sets of glands. Encotyllabe kuwaitensis n. sp. is attached individually to the lower pharyngeal plate of Caranx sp. It is characterized by having an elongate body and tandem testes. E. spari is reported from the lower pharyngeal tooth plate of Plectorhynchus cinctus, P. pictus and P. schotaf. All fish hosts were caught in Kuwaiti waters in the Arabian Gulf. The subfamily Encotyllabinae is reviewed and the genus Neoencotyllabe is regarded as a genus inquirendum. The new genus is attached to the subfamily Encotyllabinae.     

Agamococcidiorida ord. n. and Rhytidocystidae fam. n. for the Coccidian Genus Rhytidocystis Henneguy, 1907

Agamococcidiorida ord. n. and Rhytidocystidae fam. n. are established in the apicomplexan subclass Coccidiasina for the genus Rhytidocystis Henneguy, 1907. Dehornia Porchet-Henneré, 1972 is synonymized with Rhytidocystis.     

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.     

Antaretylus humus n. gen., n. sp. from the Subantarctic (Nematoda: Tylenchoidea)

Antarctylus humus n. gen., n. sp. from peat soil in the subantarctic is proposed. It can be distinguished from the most closely related genus Helicotylenchus by the arrangement of the esophageal glands, the broadly rounded lip region, and the tapering pointed tail in the female.     

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.