Genomic groups,morphology, and sectional delimitation in EurasianElymus (Poaceae,Triticeae)

Seven tetraploid species ofElymus, viz.E. sibiricus, E. caninus, E. gmelinii, E. semicostatus, E. caucasicus, E. parviglume, andE. longearistatus subsp.canaliculatus, representing five sections were studied morphologically and used in interspecific hybridizations. The aim was to investigate whether the present sectional delimitation of the genus was in agreement with genomic data and if there was a correlation between genome constitution and morphology. The study revealed: (i) further information on the genomic affinities between the different species, (ii) that there is no congruence between genome constitution of the species and current sectional delimitation, and (iii) that there is a correlation between genome constitution and morphology in the palea apex shape and in the size of cilia of the palea.     

Phenetic,biogeographical, and evolutionary study ofOrnithogalum subg.Heliocharmos (Hyacinthaceae) in the western Mediterranean basin

A macromorphological study is made on taxa of the genusOrnithogalum subg.Heliocharmos in North Africa, Spain, and France. The results obtained are consistent with data from cytogenetics, reproductive biology and strategies of reproduction. They allow the retention of two species:O. algeriense andO. umbellatum. A biogeographical and phylogenetic interpretation of the subgenus is proposed for the western Mediterranean. Theoretical views on phenetics are discussed.     

Ultrastructure of Tricornia muhezae N. G., N. Sp. (Microspora, Thelohaniidae), a Parasite of Mansonia africana (Diptera: Culicidae) from Tanzania

ABSTRACT. Collections of Mansonia africana mosquito larvae were made at one site in N.E. Tanzania in 1985 and 1987 and from two additional sites, both within about 2 mi of the original one in 1987. An octosporous microsporidian, present at all three sites, was found in both years infecting from 7 to 22% of larvae. Spores (stained in Giemsa) measured 3.0 μ m × 0.25 μ m × 2.25 μ m × 0.26 μ m. Ultrastructurally, spores were seen to have an anterior rim surrounding a depressed area where the endospore was at its thinnest. In transmission electron microscopy section, the rim appeared as two processes into which all layers of the wall extended. At the posterior end all layers of the wall extended into a simple knob-like structure which could be interpreted as a section through a crest running longitudinally around the spore. The polar filament was anisofilar, with two anterior coils of greater diameter than the three posterior coils. Although most closely resembling the genera Amblyspora and Parathelohania in the family Thelohaniidae, the species in M. africana differs from the former, which has oval spores, broadly rounded at the ends, and from the latter, which has a prominent, ridged posterior extension to the spores. The new species has been placed in a new genus and the name Tricornia muhezae proposed.     

中国的被孢霉种类

被孢霉属(Mortierella Coemans)是接合菌纲(Zygomycetes)、毛霉目(Mucorales)、被孢霉科(Mortierellaceae)中的一个大属,目前已知约有90种;主要存在于土壤、植物残体、动物粪便等基物中。我国过去对被孢霉的研究不多,在《中国真菌总汇》(1979)中记录了8个种。本研究从全国22个省、市、自治区采集的2000多号样品中,分离到约220个被孢霉菌株。本研究主要采用Gams (1970, 1977)的分类系统进行分类鉴定,并对该系统进行了修改。在属下分3个亚属(Micromucor, Mortierella和Gamsiella), 8个组(Actinomortierella, Alpina,Hygrophila, Mortierella, Schmuckii, Simplex, Spinosa和Stylospora),单囊霉(Haplosporangium)被承认为独立的一个属。本研究鉴定出22个种和3个变种,包括一个新种(武夷山被孢霉Mortierella wuyishanensis sp. nov.)和一个新变种(极细无色被孢霉Mortierella hyalina(Harz) W. Gams var. subtilissima var. nov.), 14个中国新纪录。这14个新纪录为:产芽胞被孢霉(Mortierella. gemmifera M. Ellis)、园圃被孢霉(M. horticola Linnem.)、矮小被孢霉(M. humilis Linnem.)、无色被孢霉(M. hyalina(Harz) W. Gams)、印度被孢霉(M. indica B.S. Mehrotra)、英杜被孢霉(M. indohii C.Y. Chien),詹金氏被孢霉(M. jenkinii (A.L. Sm.) Naumov)、可疑极小被孢霉(M. minutissima Tiegh. var. dubia Linnem.)、易变被孢霉(M. mutabilis Linnem.)、微孢被孢霉(M. parvispora Linnem.)、角胞拉曼被孢霉(M. ramanniana(Moller) Linnem. var. angulispora (Naumov) Linnem.)、网孢被孢霉(M. reticulata Tiegh.& G. Le Monn.)、多疣被孢霉(M. verrucosa Linnem.)、轮枝被孢霉(M. verticillata Linnem.)。文中讨论和评价了一些分类性状,还列出分亚属、分组、分种和变种的检索表.每个分类单元都有描述和讨论以及线条图、并列出分布地区。     

一种引致人体原发性皮肤毛霉病的非高温根毛霉属真菌

由石家庄中国人民解放军白求恩国际和平医院皮肤科李成龙大夫提供的一株人体皮肤病菌经我们研究鉴定为毛霉目(Mucorales)毛霉科(Mucoraceae)根毛霉属(Rhizomucor)的一个种,并定名为多变根毛霉新种(Rhizomucor variabilis Zheng & G.-q.Chen sp. nov.)。据李大夫介绍,这株菌是从一名居住在江苏农村到该医院看病的女病人的手上病部分离的。这个病人没有一般真菌病病人所患有的其他疾病如糖尿病、白血病等等。她也没有患有其他毛霉病,因此她的皮肤毛霉病是原发性的而不是继发性的。我们查阅文献结果,国内由根毛霉属真菌引致的毛霉病过去仅有过一次肺部感染的报道;国外则有过较多次数的由根毛霉引致的人体毛霉病,主要为肺部疾病并可引致继发性的皮肤病,尚未见有由根毛霉属引起的原发性皮肤毛霉病的报道。无论国内、外引起人体毛霉病的根毛霉均为微小根毛霉[Rhizomucor pusillus(Lindt) Schipper,包括Mucor pusillus Lindt,Mucor parasiticus Lucet & Costanin等异名]一种。因此,本病例为我国第二例由根毛霉弓l起的人体毛霉病及第一例由根毛霉引起的人体皮肤毛霉病,同时又是全世界第一例由根毛霉属除微小根毛霉以外的另外一个种引起的人体毛霉病,很可能还是全世界第一例由根毛霉引起的人体原发性皮肤毛霉病。多变根毛霉与根毛霉属内所有过去已报道过的种都有显著差异。它的最适生长温度为24-30℃,最低9℃,最高38℃;其他种均为高温真菌,它们的最高生长温度可达55℃或更高。形态方面,多变根毛霉也与属内其他已知种明显不同。它的菌落高达4-8 mm并呈鲜明的浅黄色;其他已知种菌落低矮,除奈尼塔尔根毛霉(Rhizomucor nainitalensis Joshi)外全部为深暗灰色,奈尼塔尔根毛霉菌落色泽虽然较浅,但为浅灰或灰黄色,与多变根毛霉的鲜明黄色不同。它的假根异常发达并可从菌体的各个部位如菌丝、匍匐丝、孢子枝、孢子囊、囊轴上长出;其他已知种的假根一般都不发达且从未见有从孢子枝、孢子囊、囊轴等处长出的描述。它的孢子枝的分枝常常长于主枝;其他已知种则分枝长度一般不超过主枝。它的囊轴形状多变:球形、近球形、扁球形、卵形、椭圆形、梨形等等,两边对称或不对称,溢缩或不绕缩,纵向深裂或不作纵向深裂;其他已知种的囊轴形状通常为倒卵形至梨形的规则形状。它的囊领明显;其他已知种的囊领均很不明显至缺如。它的孢囊孢子形状和大小变化都较大,卵形、椭圆形、矩圆形、近球形、近三角形或其他各种不规则形状,长度范围2.5-16.5 μm;其他已知种除上面已经提到过的奈尼塔尔根毛霉外,它们的孢囊孢子形状仅限于卵形、椭圆形、近球形等较规则的形状,长度范围总是在3-6 μm范围内,奈尼塔尔根毛霉的孢囊孢子形状虽然多变,但其决度亦在3-6 μm的范围内。此外,多变根毛霉的孢子囊、囊轴、孢囊孢子等各种构造均较大;其他已知种则较小,其中肿梗根毛霉[Rhizomucor tauricus (Milko & Schkurenko) Schipper]虽亦较大,但除此之外与多变根毛霉迥异。多变根毛霉未见有接合孢子,将我们保存的全部微小根毛霉菌株与它分别配对时,或将我们的几对别的属的(+)(-)测试菌株与它分别配对时,均未见形成接合孢子或有任何反应。     

中国角胫象属（鞘翅目：象虫科）

角胫象属Shirahoshizo Morimoto,1962隶属象虫科隐喙象亚科,模式种为Cryptorhynchus rufescens Roelofs.本属昆虫多寄生于松属植物,有些是我国重要林业害虫,如马尾松角胫象Shiraho shizo flavonotatus(Voss),其成虫侵入衰弱的黄山松和堆积的马尾松原木,和其它钻蛀性害虫一起,造成严重危害,据浙江亚热带林研所赵锦年先     

Chromosomal distinction between the red-faced and black-faced black spider monkeys (Ateles paniscus paniscus and A. p. chamek)

The two subspecies of the black spider monkey, Ateles paniscus paniscus and A. p. chamek, can be distinguished by their chromosome number, 2n = 32 in the former and 2n = 34 in the latter. This difference most probably is the result of a tandem fusion between chromosomes 4 and 13 of the original Ateles karyotype (2n = 34) to form a unique metacentric chromosome in A. p. paniscus. Further differences between the subspecies concern the presence of additional interstial or terminal C-bands in chromosomes 3, 5, and 12 of A. p. paniscus. A third difference is that chromosome 12 is metacentric in A. p. paniscus but is submetacentric in A. p. chamek. A. p. chamek shows dimorphisms caused by pericentric inversions in pairs 1, 5, 6, and 7 as well as in the Y chromosome. Since the dimorphisms in pairs 5 and 7 are only found in homozygous condition, they may indicate the existence of geographic variation within this subspecies. Differences in external characteristics possibly reflect these chromosomal difference. The necessity to lend A. p. paniscus full specific status should be considered, since karyologically this is the most distinct one of all forms of Ateles. In captive breeding A. p. paniscus should evidently be treated as a separate population, as hybridization with A. p. chamek may result in offspring with reduced fertility. The intra-subspecific karyological variation in A. p. chamek and its possible consequences for taxonomy and captive breeding require further investigation.     

Nolleria pulicis N. Gen., N. Sp. (Microsporida: Chytridiopsidae), a Microsporidian Parasite of the Cat Flea, Ctenocephalides felis (Siphonaptera: Pulicidae)

A new species of microsporidium, Nolleria pulicis, is described and named here from the cat flea, Ctenocephalides felis. The genus Nolleria is created and placed within the family Chytridiopsidae. The family is slightly modified to accommodate certain features of intracellular development seen in N. pulicis, which is otherwise very similar to other species in the family Chytridiopsidae. Sporulation is described from ultrastructural analysis of infected midgut epithelial cells of adult C. felis. The term “multiple division by vacuolation” is proposed for describing sporogony as it occurs in this species and certain related species of microsporidia. The probable mode of transmission and apparent absence of merogony are discussed.