鳞毛蕨科3种植物配子体发育的研究

利用光学显微镜详细观察鳞毛蕨科(Dryopteridaceae)3属3种植物,即耳蕨属的棕鳞耳蕨(Polystichum polyblepharum)、鳞毛蕨属的黑足鳞毛蕨(Dryopteris fuscipes)和鞭叶蕨属的鞭叶蕨(Cyrtomidictyum lepidocaulon)配子体发育过程,记录配子体各发育阶段的特征。结果表明:棕鳞耳蕨、黑足鳞毛蕨和鞭叶蕨的孢子都为单裂缝,孢子萌发类型为书带蕨型,配子体发育类型为三叉蕨型,性器官为薄囊蕨型,成熟原叶体为对称的心脏形,具毛状体;3属的属间差异包括孢子颜色、孢子纹饰、萌发时间、丝状体长度、片状体形状、毛状体和假根等特征,上述特征在属间存在交叉现象,因此,孢子形态和配子体发育特征不能作为区分耳蕨属、鳞毛蕨属和鞭叶蕨属的形态依据。     

中华刺蕨和长耳刺蕨配子体发育研究

采用光镜观察,对中华刺蕨和长耳刺蕨配子体发育进行了观察研究.结果表明:中华刺蕨和长耳刺蕨的孢子和配子体发育特征相似,孢子均两侧对称,单裂缝,孢子萌发方式为书带蕨型;配子体经丝状体、片状体发育为心形原叶体,毛状体多产生于幼原叶体生长点两侧边缘,为多细胞棒状,原叶体发育方式为槲蕨型;幼原叶体阶段即可产生精子器,而颈卵器只产生于大型心形原叶体生长点下方,性器官发育类型为薄囊蕨型,卵受精后发育成孢子体.该研究结果支持秦仁昌将刺蕨属和实蕨属独立为实蕨科的观点.     

国产9个蕨类植物名称的后选模式指定

种或种下分类群名称的模式(主模式、后选模式或新模式)是保存在标本馆、其它收藏处或研究机构的单份标本或插图,它是分类群名称所永久依附的成分,无论该名称是正确名称或异名。在整理保存于中国科学院植物研究所标本馆(PE)的模式标本时,根据《国际植物命名法规》(墨尔本法规)规则9.5和40.2注释1及例2,发现贵州稀子蕨(稀子蕨科)、显著节肢蕨(水龙骨科)、莫氏线蕨(水龙骨科)、卵形叶星蕨(水龙骨科)、矩圆叶石韦(水龙骨科)、峨眉凤尾蕨(凤尾蕨科)、淡色紫柄蕨(金星蕨科)、宽书带蕨(书带蕨科)、拟沿阶草叶书带蕨(书带蕨科)名称的模式为合模式。遵照规则8.1、9.11和9.12,以及辅则9A.2和9A.3的精神,对这9个名称做出后选模式指定,以规范这些名称的模式。     

铁角蕨属4种植物配子体发育的比较研究

以腐叶土为基质培养铁角蕨(Asplenium trichomanes L.)、阿尔泰铁角蕨[A.altajense(Kom.)Grubov]、假大羽铁角蕨(A.pseudolaserpitii folium Ching)和细裂铁角蕨(A.tenui folium D.Don)的孢子,用光学显微镜观察并比较它们的配子体发育过程,以期为铁角蕨属的系统学研究提供基础资料.结果显示,4种铁角蕨属植物配子体均具有:孢子两面型、单裂缝、周壁具褶皱、书带蕨型萌发,成熟原叶体心形,原叶体具有毛状体等共同特征,表明铁角蕨属的演化处于较进化的系统位置,但它们的毛状体形态和细胞数目明显不同,可为属内分系提供依据.研究发现,4种铁角蕨属植物配子体的边缘细胞形状以及假根的形态和数量均有差异,其叶绿体能象单细胞一样进行无丝分裂,强光照射下叶绿体向相邻细胞的侧壁集中等现象.     

黑龙江省蹄盖蕨科三属(蹄盖蕨属、羽节蕨属及冷蕨属)的遗传多样性分析

利用7种随机引物对分布于黑龙江省不同区域蹄盖蕨科中的蹄盖蕨属,羽节蕨属及冷蕨属三属的遗传多样性进行了初步分析,对蹄盖蕨科各种基因组的DNA进行了PCR扩增,并对其RAPD谱带进行了统计处理,得出不同区域种类的多态位点百分率,结果表明蹄盖蕨科植物具有较高水平的遗传变异,其种类的分布对周围环境变化有着较强的适应能力。利用Shannon指数和Nei指数对其分析,确定了三属之间的属内种间的亲缘关系:蹄盖蕨属的大部分变异仍存在于种源内;冷蕨属中的冷蕨和山冷蕨种类之间具有一定的遗传变异;羽节蕨属中,欧洲羽节蕨和羽节蕨种间有较大的遗传变异。     

凤尾蕨属配子体若干系统学特征新考

通过对凤尾蕨属(Pteris L.)8种,即半边旗(P.semipinnata L.)、傅氏凤尾蕨(P.fauriei Hieron.)、阔叶凤尾蕨(P.esquirolii Christ)、三叉凤尾蕨(P.tripartita Sw.)、蜈蚣草(P.vittata L.)、溪边凤尾蕨(P.excelsa Gaud.)、有刺凤尾蕨(P.setuloso-costulata Hayata)、西南凤尾蕨(P.wallichiana Agardh)孢子的人工培养,观察并总结了该属配子体发育各阶段形态特征,并与以往的观察结果进行比较.最终选取孢子萌发型与配子体发育类型等稳定特征作为判断依据,讨论该属与书带蕨科(Vittariaceae)、中国蕨科(Sinopteridaceae)、铁线蕨科(Adiantaceae)等科的亲缘关系.研究认为蕨类配子体生长点上方边缘细胞分布情况多变,不是稳定的系统学特征.而配子体特定部位边缘细胞的外侧壁形态则具有较高的系统学参考价值.     

秦岭蕨类植物区系特征及地理分布

本文论述了秦岭蕨类植物水平分布与这一地区森林分布格局是一致的,垂直分布以太白山分为4个带谱,其中以海拔800—2600米带谱内的,蕨类属种最多,约占秦岭总种数的32%。在秦岭77属中,属于热带、亚热带的属有36属,约占秦岭总属数的46.9%,其中有17个属每属仅有1种,其余每属有2—3种,均分布于秦岭南坡,这说明秦岭南坡是热带、亚热带蕨类植物分布的北缘。通过秦岭蕨类植物地理成分分析,说明秦岭蕨类植物属于喜马拉雅、中国西南到日本的蕨类植物区系,以耳蕨与鳞毛蕨为特色,称谓“耳蕨—鳞毛蕨区系”。     

东北蕨类植物配子体发育的研究Ⅷ铁角蕨科

本文研究了过山蕨配子体的发育过程。孢子左右对称,单裂缝,具周壁,孢子萌发为书带蕨型,丝状体２－７个细胞长,原叶体发育为三叉蕨型,原叶体的毛状体形状多样。性器官较小,在配子体上的此等特征说明过山蕨为进化的类型。     

黑龙江省蹄盖蕨科（Athyriaceae）植物的RAPD分析及其系统学意义

在形态分类研究的基础上,利用RAPD技术,对黑龙江省蹄盖蕨科植物6属9种共15个种群进行了遗传多样性分析,分析结果表明：（1）假冷蕨属应包括在蹄盖蕨属中（2）角蕨属与蹄盖蕨属,羽节蕨属与冷蕨属亲源关系较近（3）短肠蕨属为独立一属,与其它属亲源关系较远。根据黑龙江省蹄盖蕨科植物的DNA水平的研究结果,再结合其形态学特征,建议将黑龙江省蹄盖蕨科划分为3个亚科：冷蕨亚科（Cystopterioideae）包括2个属：冷蕨属（Cystopteris）和羽节蕨属（Cemnocarpium）。蹄盖蕨亚科（Athyrioideae）包括3个属：蹄盖蕨属（Athyrium）、假冷蕨属（Pseudocystopteris）和角蕨属（Cornopteris）。双盖蕨亚科（Diplazioideae）包括短肠蕨属（Alhntodia）。     

鳞毛蕨科植物的系统发育: 叶绿体rbcL序列的证据

运用MEGA2和MrBayes 3.0b4软件包对105种鳞毛蕨类及近缘植物(其中新测定36种)的叶绿体DNA rbcL基因序列进行系统发育分析, 探讨了其主要分类群(属级水平)的系统演化关系。用最大简约法、邻接法和贝叶斯分析方法构建的系统树基本一致, 结果显示: (1)秦仁昌系统所定义的鳞毛蕨科Dryopteridaceae, 除了拟贯众属Cyclopeltis外, 均包含在两个单系群之中, 支持鳞毛蕨族Dryopterideae和耳蕨族Polysticheae的成立; 但是鳞毛蕨族还包含秦仁昌系统所定义的球盖蕨科Peranemaceae和三叉蕨科Tectariaceae肋毛蕨属Ctenitis的部分种类; 耳蕨族还包含产于美洲的Phanerophlebia属和Polystichopsis属; 确认石盖蕨属Lithostegia属鳞毛蕨族的成员, 且与复叶耳蕨属Arachniodes具有较近的亲缘关系。(2)拟贯众属与所分析的其他任何鳞毛蕨类植物的关系都比较疏远, 单独为一支。(3)秦仁昌系统所定义的球盖蕨科与肉刺蕨属Nothoperanema聚成一个分支, 属于鳞毛蕨族的成员。(4)鳞毛蕨属Dryopteris为多系类群, 耳蕨属Polystichum和贯众属Cyrtomium均为并系类群。(5)黔蕨属Phanerophlebiopsis、毛枝蕨属Leptorumohra和石盖蕨属与复叶耳蕨属构成一支; 柳叶蕨属Cyrtogonellum与Polystichum属和Cyrtomium属的部分种类聚成一支; 肉刺蕨属与球盖蕨科及鳞毛蕨属的部分种类聚成一支。对鳞毛蕨科的系统关系、球盖蕨科与鳞毛蕨科的系统关系、肋毛蕨属与鳞毛蕨科的系统关系以及中国或亚洲特有属(拟贯众属、肉刺蕨属、黔蕨属、毛枝蕨属、石盖蕨属和柳叶蕨属)的系统位置进行了讨论。     

Significance of gametophyte form in long-distance colonization by tropical, epiphytic ferns

Gametophyte morphology of tropical epiphytic ferns may confer an advantage for establishment on islands. Most tropical, epiphytic ferns belong to five families: Hymenophyllaceae, Grammitidaceae, Vittariaceae, Polypodiaceae, and Elaphoglossaceae. Gametophytes of these families are long-lived and clone-forming. In addition, most Hymenophyllaceae, Grammitidaceae, and Vittariaceae produce dispersible gemmae. Each of these characteristics increases opportunity for outbreeding, and when island floras are statistically compared with floras of adjacent mainlands, island floras are found to be rich in epiphytic species possessing gemmae (Hymenophyllaceae, Grammitidaceae, and Vittariaceae), and depauperate in epiphytic species lacking gemmae (Polypodiaceae and Elaphoglossaceae). We propose that gametophytic gemmae significantly aid long-distance colonization of outbreeding species because gemmae 1) allow gametophytes to exploit available niches through dispersal of gemmae, and through clonal expansion and persistence of the resulting gametophyte, and 2) facilitate sexual reproduction by providing the opportunity for sperm and antheridiogen transfer when gametophytes are distant, and by providing a new source of tissue for antheridia formation.     

Studies in the Spore Morphology of Vittaria Smith

The spore morphology of 32 species of Vittaria Smith has been described. Spores are ellipsoidal or long ellipsoidal in polar view, and kidney-shaped in equatorial view, (18.2–65) × (39–110.5) × (19.5–52)μ in size, monolete, without perine. The stratification of exine which is generally 1.9–2.6 μ in thickness is distinct or indistinct. When it is distinct, the sexine is thicker than the nexine. The exine is generally orna- mented with indistinct granulose or vague sculpture, and with small verrucae in three species. In some species, there is a striate texture on the surface of the exine. As far as it goes, it is a very interesting phenomenon that has not been mentioned elsewhere in the literature of palynology. According to the references, the spores are trilete in a few species of this genus. But it is only monolete in our investigated meterial. Because the gross-morphology of plant in these genera of Vittariaceae is very similar to one anther, we raise the quastion whether the few species which have trilete spores really belong to this genus or to the other genus of Vittariaceae which have trilete, it may be further considered. On the basis of the spore types, Vittariaceae (E. B. Copeland, 1948) may be divided into two groups the one belongs to monolete spore type, and the other to trilete spore type. Based on morphology and anatomy of the plant, R. C. Ching (1940) separated out some genera which have trilete from Vittariaceae to establish a new family– Antrophyaceae, it is valuable to further exploration.     

GEMMIFEROUS FERN GAMETOPHYTES—VITTARIACEAE

Approximately 10 % of all fern species reproduce vegetatively in the gametophytic stage by means of gemmae. Gametophyte morphologies in these species depart radically from the commonly figured heart-shaped type and expand considerably the opportunities for physiological and morphological studies utilizing fern gametophytes. Original observations on four species of vittarioid ferns are presented and compared with earlier observations on gametophytes of this family. Vittarioid gametophytes grow from a discontinuous marginal meristem which results in a much branched thallus of indeterminant growth. Aerial branches of the gametophytes terminate in gemma production, which proceeds by a regular and predictable sequence of events. The sequence may differ considerably among species but is remarkably constant within species. Archegonia are produced on short ventral branches, and antheridia are produced primarily on germinating gemmae. Ananthacorus angustifolius is the only known member of the Vittariaceae which does not produce gemmae and is considered to represent the primitive condition. In this species antheridia are scattered over the thallus, suggesting that a change in the mode of control of antheridium production may have evolved in the family along with gemma production.     

中国潜跳甲属分类研究(鞘翅目:叶甲科:跳甲亚科)

本文系统研究了潜跳甲属Podagricomela Heikertinger的中国种类,共10种,包括1新记录种：黑足潜跳甲P.nigripes Medvedev。文中提供了分种检索表、简要描述和雌雄外生殖器特征图。在此基础上对本属在中国的地理分布格局进行了初步探讨。潜跳甲属Podagricomela Heikertinger的分布中心在中国,表现出由南向北分布的特点,主要分布于华南区、西南区、华中区和华北区,多以芸香科植物为寄主。     

网柄菌属的2个中国新记录种和2个中国大陆新记录种

从采自中国西南部分省区(云南、贵州)的土壤样品中分离出网柄菌属的2个中国新记录种,即粗茎网柄菌(Dictyostelium crassicaule)和交织网柄菌(Dictyostelium implicatum);2个中国大陆新记录种,即大头网柄菌(Dictyostelium macrocephalum)和大网柄菌(Dictyostelium magnum)。文中对该4个种进行了详细的形态学描述,并附其部分生活史的图片。     

The genus Andraca (Lepidoptera, Endromidae) in China with descriptions of a new species

The six species of the genus Andraca Walker hitherto known from China are reviewed, and a new species, Andraca gongshanensis, sp. n., described from Yunnan Province, China. Adults and male genitalia of all examined species are illustrated, together with a distributional map. A key to all seven Chinese Andraca species is provided. The types of the new species are deposited in SCAU (South China Agricultural University, Guangzhou, China) and HUNAU (Hunan Agricultural University, Changsha, China).     

采自长白山的几个中国新记录伞菌

报道了采自吉林省长白山自然保护区的3个中国新记录伞菌,即紫褶小孢菌[Baeospora myriadophylla(Peck)Singer]、木生囊环菇[Cystolepiota lignicola(P.Karst.)Nezdojm.]和暗褶菌[Melanophyllum haematospermum(Bull.)Kreisel],并描述了1个中国大陆新记种黄褐色孢菌[Callistosporiumluteo-olivaceum(Berk.M.A.Curtis)Singer]。Cystolepiota和Melanophyllum为中国新记录属。提供所有种的子实体照片和显微结构线条图。凭证标本存放于吉林农业大学菌物标本馆(HMJAU)。     

中国美广口蝇属(双翅目,广口蝇科)一新种及二新纪录种

记述采自中国广西大青山的美广口蝇属(双翅目,广口蝇科)一新种,广西美广口蝇Euthyplatystoma guangxiensis sp. nov..报道了2个中国新纪录种,多斑美广口蝇E.punctiplenum(Walker)(分布:云南)和明带美广口蝇E.rigidum(Walker)(分布:四川峨眉山).编制了中国美广口蝇属分种检索表.新种模式标本保存于中国科学院动物研究所,北京.     

中国三叠纪鱼类综述

三叠纪鱼类在中国分布广泛。与当时“南海北陆”的古地理格局一致,淡水鱼类主要分布于北方大陆的河湖相盆地,但也见于扬子板块与北方大陆碰撞后的四川盆地;海生鱼类则主要分布于华南和喜马拉雅地区。值得注意的是,鄂尔多斯盆地已知的三叠纪鱼类中,多数为海生类型或与海生鱼类密切相关。中国的淡水三叠纪鱼群主要由原始辐鳍鱼类组成,它们与西伯利亚和中亚的鱼群最为相近,但也有与劳业大陆其他地区及冈瓦纳大陆的鱼类相似的属种。海生鱼群则以“亚全骨鱼类”为主,并包含鲱亚部的进步类群和真骨鱼类的基干类型。华南扬子区拉丁至卡尼早期的鱼群远较早三叠世的鱼群丰富,且这一时期的鱼群与西特提斯同期的鱼群关系已极为密切,约有1/3的种类可归入相同的属。华南中下扬子区很可能是部分后来繁盛于特提斯区的三叠纪鱼类的发源地,如龙鱼类。中国的三叠纪鱼类虽然十分丰富,但大多已知鱼类仅限于零星发现和初步报道,因而仍有待全面深入的调查研究。