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1.
鄂尔多斯盆地晚石炭世孢粉组合 总被引:1,自引:0,他引:1
耿国仓 《Acta Botanica Sinica》1985,(2)
本文报道了鄂尔多斯盆地晚石炭世太原组的孢粉组合,共计68属,148种(类型)。本文描述了其中的9个新种,2个新组合和4个未定种,并建立一个组合带,即 Pseudolyosporaradialis-Gulisporites discersus-Thymospora thiessenit。根据孢粉组合情况,可看出盆地东部更接近于华北,西部则发生区系上的变化。整个孢粉组合可与盆地北缘、华北地区的太原组以及欧美等地区的维斯法期 C-D 和斯蒂芬期的孢粉组合比较。地质时代当属晚石炭世。 相似文献
2.
Microsporidia of the genus Amblyospora parasiting the adipose body of mosquito larvae of the genus Aedes and Culex has been studied with both light and electron microscopy. Six new species of microsporidia are described based on ultrastructural characteristics of spores and sporogony stages. Amblyospora flavescens sp. n. Mature spores are egg-shaped. The spore wall with three layers, about 165 nm. Exospore is two-membranous. Subexospore is absent. Endospore is electron-translucent. Polaroplast consists of three parts: lamellar, large vesicular, lamellar. The anisofilar polar filament with 10--11 coils (3 1/2 + 2 1/2 + 4-5). Fixed spores are 6.3 +/- 0.1 x 4.24 +/- 0.1 microm. Amblyospora kolarovi sp. n. Mature spores are egg-shaped. The spore wall with three layers, about 265-315 nm. Exospore shapes tucks on the surface of spore. It is two-membranous. Subexospore is quagge, structural. Endospore is electron-translucent. Polaroplast consists of two parts: lamellar and large vesicular. The anisofilar polar filament with 11-13 coils (3 + 8-10). Fixed spores are 5.4-5.6 x 3.5-4.2 microm. Amblyospora orbiculata sp. n. Mature spores are widely egg-shaped. On a back pole there is a small concavity. The spore wall with three layers, about 155 nm. Exospore is shapes tucks on a surface of spore. It is two-membranous. Subexospore is absent. Endospore is electron-translucent. Polaroplast consists of three parts: lamellar, vesicular, lamellar. Polar filament is anisofilar, with 11 1/2 coils (4 1/2 + 1 + 6). Fixed spores are 6.3 +/- 0.1 x x 4.0 +/- 0.1 microm. Amblyospora rugosa sp. n. Mature spores are egg-shaped. On a back pole there is a small concavity. The spore wall with three layers, about 225 nm. Exospore is shapes tucks on a surface of spore. It is two-membranous. Subexospore is quaggy, structural. Endospore is electron-translucent. Polaroplast lamellate. Polar filament is anisofilar, with 17 1/2 coils (3 1/2 + 1 + 13). Fixed spores are 5.3 +/- 0.1 x 3.7 +/- 0.1 microm. Amblyospora undata sp. n. Mature spores are egg-shaped. The spore wall is three-layered, about 220 nm. Exospore is shapes tucks on a surface of spore. It is two-membranous. Subexospore is quaggy, structural. Endospore is electron-translucent. Polaroplast lamellate. The anisofilar polar filament with 8 coils (3 + 5). Fixed spores are 5.0 +/- 0.1 x 3.0 +/- 0.1 microm. Amblyospora urski sp. n. Mature spores have widely oval form. The back pole is concave. The spore wall with three layers, about 280 nm. Exospore is shapes tucks on a surface of spore. It is two-membranous. Subexospore is quaggy, structural. Endospore is electron-translucent. Polaroplast lamellate. Polar filament is anisofilar, with 6 coils (2 + 4). Fixed spores are 4.4 +/- 0.1 x 2.9 +/- 0.1 microm. 相似文献
3.
Palynological studies of Early Carboniferous (Viséan) sediments of the Bonaparte Gulf Basin, northwestern Australia, reveal the presence of intact tetrahedral spore tetrads (here described as Sagenotetradites gen. nov.) and, more usually, of their disjunct spore portions which had previously been interpreted as dispersed whole-miospore species. Two species of the new tetrad genus are recognized: S. bonapartensis (Playford) comb, nov., as type species; and S. spiritensis (Playford) comb. nov. The species are distinguished, as originally, on the basis of sculptural attributes of their distal exoexines. When intact, both species share a common internal “binding” element (“Cadiospora abrupta” Playford, 1971) composed of the fused proximal exoexinal faces of all four spores of a given tetrad. Morphological comparisons with modern hepatic spores suggest an alliance of the microfossils with the order Sphaerocarpales. The occurrence of Sagenotetradites in exclusively marine sediments suggests that its parent plants grew in close proximity to the marine depositional basin. Moreover, the morphological attributes of the tetrads would appear to have facilitated dissemination by water. 相似文献
4.
CHARLES H. WELLMAN HUAICHENG ZHU JOHN E. A. MARSHALL YI WANG CHRISTOPHER M. BERRY HONGHE XU 《Palaeontology》2012,55(3):583-611
Abstract: The Lower Devonian Xujiachong Formation from the vicinity of Qujing City, Yunnan, China is interpreted as a terrestrial‐fluviatile‐lacustrine sequence. It contains important nonmarine biotas including plants, fish and invertebrates. The plants are particularly interesting as they include many endemic taxa. Dispersed spore assemblages have been recovered from the upper part of this formation. The spores are well preserved and of moderate thermal maturity. They are systematically described and four new species erected: Aneurospora xujiachongensis sp. nov., Chelinospora ouyangii sp. nov., Camptozonotriletes? luii sp. nov. and Leiozonospora xichongensis sp. nov. One new combination is proposed: Aneurospora conica (Ouyang and Lu) comb. nov. This is a rare report of a Lower Devonian dispersed spore assemblage from the South China Plate. Indeed, few dispersed spore assemblages of this age are known outside of Euramerica and Northern Gondwana. It is suggested that the Xujiachong Formation spore assemblages can all be equated to the polygonalis‐emsiensis Spore Assemblages Biozone (PE SAB) of Richardson and McGregor (1986) indicating an early (but not earliest) Pragian to ?earliest Emsian age. However, caution is urged, because biostratigraphical interpretation is difficult owing to distinct differences between dispersed spore assemblages from South China and Euramerica/Northern Gondwana. This almost certainly reflects palaeophytogeographical variation and regional endemism among early land plant floras on widely separated land masses. Palynofacies analysis supports a nonmarine origin for the deposits of the Xujiachong Formation, with the very rare marine palynomorphs that were encountered interpreted as reworked. 相似文献
5.
The myxozoans Gadimyxa atlantica n. sp. and G. sphaerica n. sp., and G. arctica n. sp. (Myxozoa, Parvicapsulidae), are described from Gadus morhua L. and Arctogadus glacialis (Peters) (Gadidae), respectively. They develop coelozoic in bisporic plasmodia in the urinary systems. Two morphological forms of spores were found in all 3 species, i.e., wide and (sub)spherical forms. Both spore types are bilaterally symmetrical along the suture line. The wide spores, semicircular in frontal view and elliptical in apical view, have 2 spherical polar capsules, which open in the sutural or median plane mid on the flat side of the spore. Mean widths of the wide spores of G. atlantica, G. sphaerica, and G. arctica are 7.5, 10.0, and 10.0 microm, respectively. The older, more thick-walled, (sub)spherical spores with binucleate sporoplasm are 8.0, 5.3, and 7.3 microm in mean width, respectively. The mean diameters of the polar capsules of (sub)spherical spores are 2.4, 1.7, and 2.2 microm, respectively. The (sub)spherical forms of Gadimyxa are most similar to Ortholinea within the Ortholineidae, but they differ in the development of the spores and in the arrangement of the polar capsules. The polychaetes Spirorbis spp. (Spirorbidae) act as invertebrate hosts of G. atlantica. The previously described actinospores of the tetractinomyxon type develop to myxospores in Gadus morhua within 8 wk. This is the second known myxozoan 2-host life cycle in the marine environment. Phylogenetic analyses based on partial small subunit rDNA sequences places Gadimyxa spp. among Parvicapsula spp. in the Parvicapsulidae. 相似文献
6.
The species of seventeen genera of Agathidinae (Braconidae) from Vietnam are revised: Agathis Latreille, 1804, Bassus Fabricius, 1804; Biroia Szépligeti, 1900; Braunsia Kriechbaumer, 1894; Camptothlipsis Enderlein, 1920; Coccygidium de Saussure, 1892; Coronagathis gen. n. (type species: Coronagathis cornifera sp. n.); Cremnops Foerster, 1862; Disophrys Foerster, 1862; Earinus Wesmael, 1837; Euagathis Szépligeti, 1900; Gyragathis gen. n. (type species: Gyragathis quyi sp. n.), Gyrochus Enderlein, 1920; Lytopylus Foerster, 1862; Therophilus Wesmael, 1837; Troticus Brullé, 1846, and Zelodia gen. n. (type species: Zelomorpha varipes van Achterberg & Maetô, 1990). Keys to the Vietnamese species are given.Sixty-five species are recognised, of which twelve species are newly recorded for Vietnam: Bassus albifasciatus (Watanabe, 1934), Coccygidium angostura (Bhat & Gupta, 1977), Cremnops atricornis (Smith, 1874), stat. n., Disophrys erythrocephala Cameron, 1900, Gyrochus yunnanensis Wang, 1984, Lytopylus romani (Shestakov, 1940), comb. n., Therophilus festivus (Muesebeck, 1953), comb. n., Therophilus javanus (Bhat & Gupta, 1977), comb. n., Therophilus lienhuachihensis (Chou & Sharkey, 1989), comb. n., Therophilus marshi (Bhat & Gupta, 1977), comb. n., Zelodia absoluta (Chen & Yang, 1998), comb. n. and Zelodia longidorsata (Bhat & Gupta, 1977), comb. n.Forty-two species are new to science: Agathis citrinisoma sp. n., Bassus albobasalis sp. n., Bassus albozonatus sp. n., Biroia soror sp. n., Braunsia bicolorata sp. n., Braunsia devriesi sp. n., Braunsia maculifera sp. n., Braunsia nigrapiculata sp. n., Braunsia pumatica sp. n., Camptothlipsis hanoiensis sp. n., Coronagathis cornifera sp. n., Earinus aurantius sp. n., Earinus brevistigmus sp. n., Euagathis flavosoma sp. n., Disophrys maculifera sp. n., Disophrys quymanhi sp. n., Disophrys rhinoides sp. n., Gyragathis quyi sp. n., Therophilus annuliferus sp. n., Therophilus cattienensis sp. n., Therophilus contrastus sp. n., Therophilus crenulisulcatus sp. n., Therophilus depressiferus sp. n., Therophilus elongator sp. n., Therophilus levisoma sp. n., Therophilus marucae sp. n., Therophilus mellisoma sp. n., Therophilus nigrolineatus sp. n., Therophilus nuichuaensis sp. n., Therophilus parasper sp. n., Therophilus planifrons sp. n., Therophilus punctiscutum sp. n., Therophilus robustus sp. n., Therophilus rugosiferus sp. n., Therophilus scutellatus sp. n., Troticus alloflavus sp. n., Troticus giganteus sp. n., Zelodia albobasalis sp. n., Zelodia anginota sp. n., Zelodia bicoloristigma sp. n., Zelodia brevifemoralis sp. n. and Zelodia flavistigma sp. n.The following new synonyms are proposed: Euagathis nigrithorax Bhat & Gupta, 1977, Euagathis variabilis Enderlein, 1920, Euagathis variabilis var. tibialis Enderlein, 1920, Euagathis variabilis var. melanopleura Enderlein, 1920 and Euagathis variabilis var. sucarandana Enderlein, 1920 with Euagathis abbotti (Ashmead, 1900); Euagathis jinshanensis Chen & Yang, 2006 and Euagathis sharkeyi Chen & Yang, 2006, with Euagathis forticarinata (Cameron, 1899). The genus Amputostypos Sharkey, 2009, is synonymised with Coccygidium de Saussure, 1892, syn. n.The following new combinations are given: Bassus subrasa (Enderlein, 1920), comb. n., Gyragathis angulosa (Bhat & Gupta, 1977), comb. n., Lytopylus romani (Shestakov, 1940), comb. n., Therophilus annulus (Chou & Sharkey, 1989), comb. n., Therophilus asper (Chou & Sharkey, 1989), comb. n., Therophilus cingulipes (Nees, 1812), comb. n., Therophilus daanyuanensis (Chen & Yang, 2006), comb. n., Therophilus fujianicus (Chen & Yang, 2006), comb. n., Therophilus javanus (Bhat & Gupta, 1977), comb. n., Therophilus lanyuensis (Chou & Sharkey, 1989), comb. n., Therophilus luzonicus (Bhat & Gupta, 1977), comb. n., Therophilus muesebecki (Bhat & Gupta, 1977), comb. n., Therophilus rudimentarius (Enderlein, 1920), comb. n., Therophilus similis (Bhat & Gupta, 1977), comb. n., Therophilus sungkangensis (Chou & Sharkey, 1989), comb. n., Therophilus tanycoleosus (Chen & Yang, 2006), comb. n., Therophilus tonghuaensis (Chen & Yang, 2006), comb. n., Therophilus tongmuensis (Chen & Yang, 2006), comb. n., Therophilus transcasperatus (Chen & Yang, 2006), comb. n., Troticus latiabdominalis (Bhat, 1978),comb. n., Zelodia absoluta (Chen & Yang, 1998), comb. n., Zelodia achterbergi (Chen & Yang, 2006), comb. n., Zelodia albopilosella (Cameron, 1908), comb. n., Zelodia chromoptera (Roman, 1913), comb. n., Zelodia nihonensis (Sharkey, 1996), comb. n., Zelodia cordata (Bhat & Gupta, 1977), comb. n., Zelodia diluta (Turner, 1918), comb. n., Zelodia dravida (Bhat & Gupta, 1977), comb. n., Zelodia exornata (Turner, 1918), comb. n., Zelodia longidorsata (Bhat & Gupta, 1977), comb. n., Zelodia longiptera (Yang & Chen, 2006), comb. n., Zelodia maculipes (Cameron, 1911), comb. n., Zelodia nigra (Bhat & Gupta, 1977), comb. n., Zelodia philippinensis (Bhat & Gupta, 1977), comb. n., Zelodia reticulosa (Yang & Chen, 2006), comb. n., Zelodia quadrifossulata (Enderlein, 1920), comb. n., Zelodia ruida (Sharkey, 1996), comb. n., Zelodia similis (Bhat & Gupta, 1977), comb. n., Zelodia penetrans (Smith, 1860), comb. n. and Zelodia varipes (van Achterberg & Maetô, 1990), comb. n. 相似文献
7.
Aken'Ova TO 《Systematic parasitology》2007,67(1):25-42
The similarities between Opecoelus Ozaki, 1925, Coitocaecum Nicoll, 1915, Opegaster Ozaki, 1928 and Paropecoelus Pritchard, 1966 and the difficulty of separating Opecoelus and Opegaster are discussed. It is proposed that Opegaster be reduced to synonymy with Opecoelus and the diagnosis of the latter amended to accommodate both forms. Four new species of Opecoelus are described from marine teleosts in Australian waters. These are Opecoelus woolcockae n. sp. from Acanthopagrus butcheri and A. australis from off South Australia, New South Wales and southern Queensland, O. pomatomi n. sp. from Pomatomus saltatrix off New South Wales, O. crowcrofti n. sp. from Atherinomorus ogilbyi off southern Queensland and O. queenslandicus n. sp. from Apogon fasciatus off southern Queensland. The following new combinations are formed: Opecoelus gonorhynchi (Gavrilyuk, 1979) n. comb., O. elongatus (Yamaguti, 1959) n. comb., O. pentadactylus (Manter, 1940) n. comb., O. apogonichthydis (Yamaguti, 1938) n. comb., O. cameroni (Caballero & Caballero, 1969) n. comb., O. dendrochiri (Yamaguti, 1970) n. comb., O. hawaiiensis (Yamaguti, 1970) n. comb., O. jamunicus (Srivastava, 1968) n. comb., O. longivesiculus (Yamaguti, 1952) n. comb., O. mastacembalii (Harshey, 1937) n. comb., O. mehrii (Harshey, 1937) n. comb., O. synodi (Manter, 1947) n. comb., O. tamori (Yamaguti, 1938) n. comb., O. bothi (Yamaguti, 1970) n. comb., O. caulopsettae (Manter, 1954) n. comb., O. beliyai (Pande, 1937) n. comb., O. brevifistulus (Ozaki, 1928) n. comb., O. cryptocentri (Yamaguti, 1958) n. comb., O. dactylopteri (Yamaguti, 1970) n. comb., O. dermatogenyos (Yamaguti, 1970) n. comb., O. ditrematis (Yamaguti, 1942) n. comb., O. gobii (Yamaguti, 1952) n. comb., O. hippocampi (Shen, 1982) n. comb., O. iniistii (Yamaguti, 1970) n. comb., O. lobulus (Wang, 1977) n. comb., O. macrorchis (Yamaguti, 1938) n. comb., O. parapristipomatis (Yamaguti, 1934) n. comb., O. pritchardae (Overstreet, 1969) n. comb., O. syngnathi (Yamaguti, 1934) n. comb., O. lutiani (Bravo-Hollis & Manter, 1957) n. comb., O. ovatus (Ozaki, 1928) n. comb., O. plotosi (Yamaguti, 1940) n. comb. and O. rectus (Ozaki, 1928) n. comb.; all the new combinations were previously species of Opegaster. 相似文献
8.
CHRISTER ERSUS 《Zoologica scripta》1984,13(4):239-272
The gutless members of the subfamily Phallodrilinae are taxonomically revised and generically split off from their gut-bearing relatives. Inanidrilus Erséus, 1979, a much modified definition of which is presented, comprises the species leukodermatus (Giere, 1979) comb.n., speroi sp.n., fijiensis sp.n., bonomii sp.n., carterensis sp.n., gustavsoni sp.n., wasseri sp.n., scalprum sp.n., belizensis sp.n., aduncosetis sp.n., vacivus sp.n., triangulatus sp.n., ernesti sp.n., manae sp.n., falcifer Erséus & Baker, 1982, renaudae sp.n., extrmus (Erséus 1979) comb.n., mexicanus Erséus & Haker, 1982, and bulbosus Erséus, 1979. Olavius sp.n. is established to accommodate the species geniculatus (Erséus, 1981) comb.n., imperfectus sp.n., filithecatus (Erséus. 1981) comb.n. albidus (Jamieson, 1977) comb.n., propinquus sp.n., comorensis (Erséus. 1981) comb.n., cornuatus Davis, 1984, pellucidus sp.n., tenuissimus (Erséus, 1979) macer sp.n., caudatus (Erséus. 1979) comb.n., planus (Erséus, 1979) comb.n., clavatus (Erséus. 1981) comb.n., tantulus sp.n., longissimus (Giere, 1979) comb.n., alius sp.n., avisceralis (Erséus, 1981) comb.n., loisae sp.n., and hanssoni sp.n., Two subgenera are erected for tantulus—longissimus–alius (nominate subgenus Olavius) and avisceralis-loisae-hanssoni (Coralliodriloides subgen.n.), respectively. A tentative phylogeny of the gutless group, which appears monophyletic, is inferred on the basis of a partly computerized Wagner-tree analysis of all 38 species. According to this analysis. According to this analysis, Inanidrilus can be defined by one synapomorphy, more or less sickle-shaped penial setae, whereas Olavius can be discriminated by two such characters, (1) atrium comma-shaped/horizontal rather than erect and (2) copulatory sacs present. 相似文献
9.
The microsporidium Unikaryon polygraphi sp.n., a pathogen of Polygraphus poligraphus in Austria is described based on light microscopic and ultrastructural characteristics. All life stages have isolated nuclei. Sporogony ends with uninucleate single sporoblasts and spores. Mature oval spores measure 2.5–3.0 μm × 1.0–1.5 μm. The larger spores (3 × 1.5 μm) belong to the `early spore type' with a polar filament coiled in five turns and the smaller spores (2.5 × 1 μm) with polar filament coiled in 6/7 turns belong to the `environmental spore type'. Columnar cells of the midgut, longitudinal and circular muscles and the secretory part of Malpighian tubules of adult beetles are infected. Mature spores are excreted together with the faeces. 相似文献
10.
Deng Sheng-hui 《植物学报(英文版)》1995,37(6)
Based upon the characters of the fertile segments and the reproductive structures, four early Cretaceous monolete spore ferns: Athyrium asymmetricum (Meng) comb. nov. of Athyriaceae, Asplenium popovii Samylina of Aspleniaceae, Dryopterites gracilis sp. nov. and D. liaoningensis sp. nov. of Dryopteriaceae have been described from Xiaoming′anbei Formation, Tiefa Basin, Liaoning Province, China. 相似文献
11.
R. H. L. DISNEY 《Systematic Entomology》1990,15(3):305-320
Abstract. The genus Couturiera Disney, 1979, only known in the female sex, is synonymized with Perissa Borgmeier, 1967, only known in the male sex, a syn.n., thus solving the problem of the 'missing' males of the Alamirinae. Perissa kensmithi (Disney) comb.n., P.lewisi (Disney) comb.n. and P.orientalis (Disney & Peterson) comb.n. are transferred from Couturiera. Perissa couturieri Disney is synonymized under P. lewisi (Disney) and C.palawanensis Disney under P.georgei Disney. Perissa latiptera sp.n., P.oligoseta sp.n., P.tinglei sp.n. and Perittophora couturieri gen.n., sp.n., are described from Zimbabwe. A key to the twelve species of Alamirinae is provided. It is hypothesized that the Alamirinae may be paraphyletic, by virtue of exclusion of the Termitoxeniinae. The latter is probably polyphyletic, in that each Alamirinae genus is probably the sister group of a different Termi-toxeniin clade. 相似文献
12.
Two fertile ferns from the Stephanian of the Massif Central (France) are described in detail. One has been found in the Blanzy basin and is assigned to Oligocarpia (Sphenopteris) leptophylla (Bunbury) nov. comb., according to the morphology of the sterile pinnae and of the fructifications. Its spores agree with the «sporae dispersae Granulatisporites parvus (Ibr.) Potonié and Kremp. The other fern has been collected in the St Etienne basin and is assigned to Senftenbergia plumosa (Artis) Radforth var. ligerensis nov. var. Its spores agree with the morphographic genus Raistrickia (S., W. and B.) Potonié and Kremp but do not look like any described species; therefore the new species name R. polymorpha nov. sp. has been given to that spore. 相似文献
13.
14.
J. I.RONNY LARSSON 《The Journal of eukaryotic microbiology》1990,37(4):310-318
The microsporidium Nudispora biformis n. g., n. sp., a parasite of a larva of the damsel fly Coenagrion hastulatum in Sweden, is described based on light microscopic and ultrastructural characteristics. Merogonial stages and sporonts are diplokaryotic. Sporogony comprises meiotic and mitotic divisions, and finally eight monokaryotic sporoblasts are released from a lobed plasmodium. Sporophorous vesicles are not formed. The monokaryotic spores are oval, measuring 1.4–1.8 × 2.8–3.4 μm in living condition. The thick spore wall has a layered exospore, with a median double-layer. The polaroplast has two lamellar parts, with the closest packed lamellae anteriorly. The isofilar polar filament is arranged in 6 (to 7) coils in the posterior half of the spore. Laminar and tubular extracellular material of exospore construction is present in the proximity of sporogonial stages. In addition to normal spores teratological spores are produced. The microsporidium is compared to the microsporidia of the Odonata; its possible relations to the genus Pseudothelohania and to the Thelohania-like microsporidia are discussed. The new genus is provisionally included in the family Thelohaniidae. 相似文献
15.
Shaun L Winterton Michael E Irwin & David K Yeates 《Australian Journal of Entomology》1999,38(4):274-290
The phylogenetic relationships of the Taenogera genus-group, consisting of nine genera, are examined using cladistic methods. Twenty-one species representing nine genera and one outgroup were compared in a cladistic analysis across 99 states in 44 characters. The genus Taenogera Kröber is revised to contain only T. longa (Schiner), T. nitida (Macquart) and T. notatithorax Mann. Two new genera are described and figured: Actenomeros gen. n., with two species, A. corniculaticaudus sp. n. and A. onyx sp. n.; and Taenogerella gen. n., with four species, Ta. elizabethae sp. n., Ta. platina sp. n., Ta. schlingeri sp. n. and Ta . nigrapicalis (Mann) comb. n. Phylogenetic analysis also supports the removal of Nanexila gracilis (Mann) comb. n. from Taenogera . 相似文献
16.
We revise the genus Opisthoscelis Schrader, and erect the genus Tanyscelisgen. n. with Opisthoscelis pisiformis Froggatt as its type species. Species of both genera induce sexually dimorphic galls on Eucalyptus (Myrtaceae) in Australia, with Opisthoscelis subrotunda Schrader also in Papua New Guinea. We synonymise the following taxa (junior synonym with senior synonym): Opisthoscelis fibularis Froggatt, syn. n. with Opisthoscelis spinosa Froggatt; Opisthoscelis recurva Froggatt, syn. n. with Opisthoscelis maculata Froggatt; Opisthoscelis globosa Froggatt, syn. n. (= Opisthoscelis ruebsaameni Lindinger) with Opisthoscelis convexa Froggatt; and Opisthoscelis mammularis Froggatt, syn. n. with Opisthoscelis verrucula Froggatt. We transfer seven Opisthoscelis species to Tanyscelis as Tanyscelis conica (Fuller), comb. n., Tanyscelis convexa (Froggatt), comb. n., Tanyscelis maculata (Froggatt), comb. n., Tanyscelis maskelli (Froggatt), comb. n., Tanyscelis pisiformis (Froggatt), comb. n., Tanyscelis spinosa (Froggatt), comb. n., and Tanyscelis verrucula (Froggatt), comb. n. We redescribe and illustrate the adult female of each named species of Opisthoscelis for which the type material is known, as well as the first-instar nymph of the type species of Opisthoscelis (Opisthoscelis subrotunda) and Tanyscelis (Opisthoscelis pisiformis). We describe four new species of Opisthoscelis: Opisthoscelis beardsleyi Hardy & Gullan, sp. n., Opisthoscelis thurgoona Hardy & Gullan, sp. n., Opisthoscelis tuberculataHardy & Gullan, sp. n., and Opisthoscelis ungulifinis Hardy & Gullan, sp. n., and five new species of Tanyscelis: Tanyscelis grallator Hardy & Gullan, sp. n., Tanuscelis megagibba Hardy & Gullan, sp. n., Tanyscelis mollicornuta Hardy & Gullan, sp. n., Tanyscelis tripocula Hardy & Gullan, sp. n., and Tanyscelis villosigibba Hardy & Gullan, sp. n. We designate lectotypes for Opisthoscelis convexa, Opisthoscelis fibularis, Opisthoscelis globosa Froggatt, Opisthoscelis maculata, Opisthoscelis mammularis, Opisthoscelis maskelli, Opisthoscelis pisiformis, Opisthoscelis recurva, Opisthoscelis serrata, Opisthoscelis spinosa, and Opisthoscelis verrucula. As a result of our taxonomic revision, Opisthoscelis has six species and Tanyscelis has 12 species. We describe the galls of females for all 18 species and galls of males for 10 species of Opisthoscelis and Tanyscelis, and provide photographs of the galls for most species. A key to the adult females of the species of both genera is included. 相似文献
17.
Occurrence of a new microsporidan: Enterocytozoon bieneusi n.g., n. sp., in the enterocytes of a human patient with AIDS 总被引:28,自引:0,他引:28
I Desportes Y Le Charpentier A Galian F Bernard B Cochand-Priollet A Lavergne P Ravisse R Modigliani 《The Journal of protozoology》1985,32(2):250-254
A new microsporidium is reported infesting the enterocytes of a Haitian patients with AIDS. The stages observed were diplokaryotic cells, sporogonial plasmodia, unikaryotic sporoblasts, and spores. Neither a sporophorous vesicle (pansporoblastic membrane) nor parasitophorous vacuole were differentiated around the developmental stages, which were in direct contact with the host cell cytoplasm. The polar tube (5-6 coils) was differentiated before fission of the sporogonial plasmodium. The mature spores measured 1.5 micron X 0.5 micron. The spore wall was very thin as the endospore was absent or poorly differentiated. The organism is named Enterocytozoon bieneusi n. g., n. sp. and is assigned to the suborder Apansporoblastina. 相似文献
18.
Two new species of Myxozoa from the brain of the green knife fish Eigemannia virescens are described: Myxobolus inaequus sp. n. has an unusually large spore body and extremely unequal polar capsules, and Henneguya theca sp. n. has an attenuated spore encased in a sheath not previously described in other Myxozoa . Only spores of the two species were observed, and infections caused no obvious pathological changes in the brain. 相似文献
19.
ROBERT E. OLSON KENNETH L. TIEKOTTER PAUL W. RENO 《The Journal of eukaryotic microbiology》1994,41(4):349-359
ABSTRACT. The microsporidium Nadelspora canceri n. g., n. sp., is described from the striated musculature of the Dungeness crab ( Cancer magister ) in Oregon, USA. The needle-shaped spores were rounded anteriorly, tapered to a posterior point and measured 7.1–11.8 × 0.2–0.3 μm in fixed preparations. The extremely narrow spore diameter prevented observation of morphological details at the light microscopic level and ultrastructural details of mature spores were difficult to resolve. Meronts were not observed and the monokaryotic merozoites and sporonts were not contained within either parasitophorous or sporophorous vesicles. Sporonts were disporoblastic and gave rise to monokaryotic sporoblasts that became narrow and elongate as they developed into immature spores with a developing polar filament. The nucleus was not clearly resolved in mature spores and may have been surrounded by the lamellar polaroplast. The polar filament was of nearly uniform diameter throughout most of its length and ended abruptly about three-fourths of the distance from the anterior end of the spore. Unusual spherical non-membrane bound granules surrounded the polar filament in a spiral arrangement. The new microsporidium resembles members of the family Mrazekiidiae, but differs in lacking a diplokaryon at any stage. It is probably most closely related to Baculea daphniae from which it differs primarily by spore shape and size. The familial relationships of the genus Baculea have not been determined and it is proposed to include it with Nadelspora in the new family Nadelsporidae. 相似文献
20.
The Australian Thrasorinae are revised and Mikeius is transferred to Mikeiinae Paretas-Martínez & Pujade-Villar, subfam. n., and Mikeius clavatus Pujade-Villar & Restrepo-Ortiz, sp. n., is described. Two new genera of Thrasorinae are erected: Cicatrix Paretas-Martínez, gen. n., including Cicatrix pilosiscutum(Girault), comb. n. from Amblynotus, Cicatrix schauffi (Buffington), comb. n. from Mikeius, and Cicatrix neumannoides Paretas-Martínez & Restrepo-Ortiz, sp. n.; and Palmiriella Pujade-Villar & Paretas-Martínez, gen. n., including Palmiriella neumanni (Buffington), comb. n. from Mikeius, Thrasorus rieki Paretas-Martínez & Pujade-Villar, sp. n., is also described. A phylogenetic analysis of 176 morphological and biological characters, including all these new taxa and all genera previously included in Thrasorinae, was conducted. All subfamilies were recovered as monophyletic, with the following relationships: Parnipinae (Euceroptrinae (Mikeiinae (Plectocynipinae (Thrasorinae)))). A worldwide key to the subfamilies of Figitidae is provided that includes the new subfamily, as well as a key to genera Thrasorinae. 相似文献