中国蕨类植物孢子形态的研究Ⅲ.金星蕨科1.毛蕨属

利用扫描电镜对中国产毛蕨属51种植物孢子形态进行了研究。结果表明：该属孢子为单裂缝,两侧对称,极面观为椭圆形,赤道面观为肾形,由周壁形成表面纹饰。表面纹饰可分为3种类型：(1)周壁具流苏状的翅状纹饰,表面有突起或穿孔,有19种属于此类型;(2)鸡冠状纹饰,有11种属于此类型;(3)刺状纹饰,有10种属于此类型。另外有11种具有上述纹饰的混合纹饰,被认为是中间类型。孢子的形态特征可作为该属的分类学和孢粉学研究的资料。     

中国蕨类植物孢子形态的研究 Ⅱ. 中国蕨科

利用扫描电镜对国产中国蕨科Sinopteridaceae植物9属61种6变种的孢子进行了观察。结果表明,该科植物的孢子可分为3种类型：(1)孢子球形,三裂缝;周壁较厚,疏松地包在孢子之外;外壁光滑,表面纹饰由周壁形成,呈网状、嵴状、刺状或皱状。除金粉蕨属Onychium和珠蕨属Cryptogramma外,该科其他属的植物都具此类型孢子。(2)孢子钝三角形,三裂缝;周壁较薄,由周壁和外壁共同形成表面轮廓,表面具疣状或颗粒状纹饰。具此类型孢子的只有珠蕨属。(3)孢子钝三角形,三裂缝,沿裂缝两侧各有一脊状隆起或瘤状纹饰;周壁薄,由外壁形成表面纹饰的基本轮廓;具赤道环、近极脊和远极脊。具此类型孢子的只有金粉蕨属。另外,从孢粉学的角度对该科的分类和系统演化进行了探讨。     

中国蕨类植物孢子形态的研究Ⅷ.岩蕨科

利用扫描电镜对中国产岩蕨科(Woodsiaceae)3属18种植物孢子进行了观察。结果表明,孢子单裂缝,两侧对称,极面观为椭圆形或宽椭圆形,赤道面观为半圆形或超半圆形;极轴长32～50μm,赤道轴长43～61μm;外壁表面光滑,由周壁形成孢子表面纹饰的轮廓,根据表面纹饰,孢子可分为5种类型:(1)片状纹饰:周壁表面形成疏密不一的片状褶皱,并连成网状;(2)脊状纹饰:周壁表面形成脊状褶皱,并连成网状;(3)翅脊状纹饰:周壁表面具脊状褶皱,并连成网状,脊的顶端具流苏状不明显的低翅;(4)翅状纹饰:周壁外层形成翅状纹饰,翅的边缘较薄;(5)丝毛状纹饰:周壁结构疏松,由细丝交织成立体网状。上述孢粉学特征表明,岩蕨科是一个自然的类群,其3属的亲缘关系较近,都是岩蕨科的合理成员。     

中国蕨类植物孢子形态的研究IV. 金星蕨科2

利用扫描电镜对中国产金星蕨科Thelypteridaceae 14属50种植物孢子形态进行了研究。孢子单裂缝,两侧对称,极面观为椭圆形、阔椭圆形或近圆形,赤道面观为肾形或圆形。极轴长为16.8-40.5 um,赤道轴长为12.8-58 um。根据表面纹饰,孢子可分为7种类型。(1)平滑:周壁表面光滑,少纹饰,如延羽卵果蕨Phegopteris decursive-pinnata。(2)网状纹饰:周壁外层形成绳索状条纹交织成网,如紫柄蕨属Pseudophegopteris。(3)环状纹饰:周壁外层形成由绳索状丝构成的环,排列在周壁表面呈网状、不规则网状或分散的网状。如方秆蕨属Glaphyropteridopsis和针毛蕨属Macrothelypteris的针毛蕨M. oligophlebia。(4)具流苏的翅状纹饰:周壁向外形成薄片状翅,翅的边缘流苏状或具齿,片连接成网状或拟网状。如金星蕨属Parathelypteris的海南金星蕨P. subimmersa、光脚金星蕨P. japonica、钝角金星蕨P. angulariloba,钩毛蕨属Cyclogramma的耳羽钩毛蕨C. auriculata,针毛蕨属Macrothelypteris的大部分种类和毛蕨属Cyclosorus的部分种类。(5)具穿孔的脊状纹饰:周壁向外形成高或低、窄或宽的脊状纹饰连接成网状或拟网状,脊上具大小不一的穿孔。如金星蕨属、龙津蕨属Mesopteris、凸轴蕨属Metathelypteris和卵果蕨P. connectilis。(6)鸡冠状纹饰:周壁形成的短翅或短的片状脊,呈鸡冠状。如毛蕨属Cyclosorus的大部分种类。(7)刺状纹饰:周壁表面形成各种刺状纹饰,如茯蕨属Leptogramma、圣蕨属Dictyocline、沼泽蕨属Thelypteris、普通假毛蕨Pseudocyclosorus subochthodes、钩毛蕨属的大部分种类和毛蕨属Cyclosorus的部分种类。根据孢子形态特征,对本科的一些属的关系进行了探讨。     

中国蕨类植物孢子形态研究Ⅸ.阴地蕨科

利用扫描电镜对国产阴地蕨科(Botrychiaceae)3属12种植物孢子进行了观察.结果表明: 孢子具三裂缝;极面观为钝三角形或近圆形;赤道面观为半圆形或超半圆形.极轴长20～34 μm,赤道轴长31～40 μm.由外壁形成孢子表面纹饰的轮廓;周壁薄,疏松地覆盖在外壁表面.孢子表面纹饰可分为以下3种类型:①疣块状纹饰(verrucate-rugulate):孢子远极面形成顶端扁平而大的疣块状纹饰,再由疣块连接成短的条状或拟网状;②疣状纹饰(verrucate):孢子表面具大小不等的疣状纹饰,相邻的疣愈合成短条状或不愈合;③脊状纹饰(lophate):孢子表面具脊状褶皱,并连接成网状.从孢子形态、纹饰类型和孢壁结构看3属属内差异明显,属间差异不明显,研究结果支持阴地蕨科具1属--阴地蕨属,其下可分3个组.     

中国蕨类植物孢子形态的研究 Ⅰ. 海金沙科

此文是中国蕨类植物孢子形态研究的第一部分。首次利用扫描电镜对国产海金沙科Lygodiaceae 海金沙属Lygodium 10种植物的孢子形态进行了观察,并利用透射电镜对孢壁的结构进行了研究。此 外,还对采自国外的另外10种海金沙属植物的孢子进行了比较观察。海金沙属孢子为三裂缝,少数为单 裂缝,其表面纹饰可分为4种类型：①瘤状纹饰,海金沙属多数种类的孢子具此类型;②表面平滑,L. palmatum、L. subareolatum、L．yunnanense、L. volubile 等属此类型;③疣状纹饰,L. dimorphum、L．digita- tum、L. kingii等属此类型;④网穴状纹饰,L. scandens,L．reticulatum等属此类型。网状纹饰类型的孢子表面轮廓是由外壁形成,其余类型的孢子表面轮廓由周壁形成。此文还对海金沙属的孢子特征及其在分类上的意义进行了探讨。     

中国蕨类植物孢子形态的研究 Ⅵ . 凤尾蕨科

利用扫描电镜对国产凤尾蕨科( Pteridaceae ) 2 属30 种4 变种植物孢子进行了观察。其中凤尾蕨属( Pteris) 29 种4 变种, 孢子三裂缝, 辐射对称; 极面观为钝三角形, 赤道面观为半圆形或超半圆形; 孢子极轴长26～54μm, 赤道轴长34～97μm; 外壁厚, 形成孢子表面纹饰的轮廓; 周壁薄, 紧贴于外壁上; 多数种类孢子外壁具沿赤道加厚的赤道环, 孢子表面呈瘤块状、疣块状, 或隆起的脊连成网状或拟网状等纹饰, 有的种类具近极脊和远极脊。凤尾蕨属植物孢子的形态稳定, 种间差异明显, 但孢子形态特征与孢子体的形态特征是不相关的。栗蕨属( Histiopteris) 植物孢子为单裂缝, 两侧对称, 极面观椭圆形, 赤道面观豆形; 孢子极轴长22～23μm, 赤道轴长29～36μm; 周壁很薄, 由外壁形成孢子纹饰的轮廓; 表面呈粗的块状纹饰。从孢子形态上看, 栗蕨属与凤尾蕨属有很大差异, 将其放在一个科中不合适。     

中国蕨类植物孢子形态的研究Ⅵ.凤尾蕨科

利用扫描电镜对国产凤尾蕨科(Pteridaceae)2属30种4变种植物孢子进行了观察。其中凤尾蕨属(Pteris)29种4变种,孢子三裂缝,辐射对称;极面观为钝三角形,赤道面观为半圆形或超半圆形;孢子极轴长26~54μm,赤道轴长34~97μm;外壁厚,形成孢子表面纹饰的轮廓;周壁薄,紧贴于外壁上;多数种类孢子外壁具沿赤道加厚的赤道环,孢子表面呈瘤块状、疣块状,或隆起的脊连成网状或拟网状等纹饰,有的种类具近极脊和远极脊。凤尾蕨属植物孢子的形态稳定,种间差异明显,但孢子形态特征与孢子体的形态特征是不相关的。栗蕨属(Histiopteris)植物孢子为单裂缝,两侧对称,极面观椭圆形,赤道面观豆形;孢子极轴长22~23μm,赤道轴长29~36μm;周壁很薄,由外壁形成孢子纹饰的轮廓;表面呈粗的块状纹饰。从孢子形态上看,栗蕨属与凤尾蕨属有很大差异,将其放在一个科中不合适。     

秦岭耳蕨属孢子形态研究

本文在经典分类基础上,就秦岭地区常见的7种耳蕨属(Polystichum)植物,采用光学显微镜和扫描电子显微镜,对其孢子形态进行了系统的观察。在扫描电镜下,从形态和周壁纹饰上可将孢子分为两种类型:一种是周壁具明显的褶皱,其表面分布稀疏或较密集的小瘤状或小疣状突起,无穿孔;另一种周壁较薄,褶皱具明显穿孔,穿孔大小及形状不一致,周壁表面有颗粒状或小刺状突起。研究表明,孢子形态、周壁纹饰在种间具有明显差异,从而可为本属种间分类提供孢粉学依据。     

中国介蕨属孢子形态的研究

采用光学显微镜和扫描电子显微镜对国产介蕨属Dryoathyrium 14种植物及宁陕蛾眉蕨Lunathyri- um ningshenense 的孢子形态进行了观察。介蕨属孢子单裂缝,两侧对称,极面观为椭圆形,赤道面观为半 圆形或肾形。根据其周壁褶皱隆起形成的表面纹饰,介蕨属孢子可分为3种类型：第一种类型的周壁 具有网状或拟网状脊状纹饰,具此类型的种有翅轴介蕨D．pterorachis,中华介蕨D．chinense,朝鲜介蕨 D．coreanum;第二种类型的周壁具有裂片状、弯裂片状或瘤状突起,具此类型的种有介蕨D．boryanum, 陕甘介蕨D．confusum,无齿介蕨D．edentulum,鄂西介蕨D.henryi,华中介蕨D．okuboanum,川东介 蕨D．stenopteron,刺毛介蕨D．setigerum,绿叶介蕨D．viridifrons;第三类型的周壁具有刺状、不规则 棒状或乳头状突起,具此类型的种有直立介蕨D．erectum,镰小羽介蕨D．falcatipinnulum,蛾眉介蕨D． unifurcatum。宁陕蛾眉蕨的孢子形态与朝鲜介蕨D．coreanum 十分相似,支持将前者作为后者的异名的分类处理。     

Spore Morphology of Pteridophytes from China Ⅵ .Pteridaceae

The spore morphology of 30 species 4 variety of 2 genera of Pteridaceae from China was investigated under scanning electron microscope (SEM) . Among them, 29 species 4 variety belong to the genus Pteris . The spores of Pteris are trilete , radiosymmetrical , subtriangular in polar view and hemispherical or subhemispherical in equatorial view . The polar axes are 26 - 54μm long , and equatorial axes are 34 - 97μm long . The perispore is thin and the surface ornamentation is formed by the exospore . The types of ornamentation are tuberculiform-rugulate , verruciform-rugulate or lophate , the spore of most species with the equatoial flange, some species with proximal ridge and distal ridge . The spore morphology of Pteris is stable, and the difference between species is distinct , but the features of spore and sporophyte are not related. The spore of Histiopteris is monolete and bilaterally symmetrical, elliptical in polar view and kidney-shaped in equatorial view . The polar axes are 22 - 23μm long , and equatorial axes are 29 - 36 μm long . The perispore is thin and the surface ornamentation is formed by the exospore . The surface is rugulate . The spore morphology of Histiopteris and Pteris is very differential , put genus Histiopteris in family Pteridaceae is not suitable, according to the feature of spore morphology .     

Spore morphology of pteridophytes from China Ⅰ. Lygodiaceae

This paper is the first report of an investigation on the spore morphology of Chinese ferns. Spore morphology of 20 species (10 species from China and 10 species from other countries) in the genus Lygodium (Lygodiaceae) was investigated under scanning electron microscope (SEM) and transmission electron microscope (TEM). The spores are tetrahedral-globose, trilete, rarely monolete. The surface ornamentation of the spores can be divided into four main types: In type I , the surface of spores is tuberculate or spheroid-tuberculate. Most of the species of the genus have this type of surface ornamentation of spores. In type II , the surface of spores is smooth. L. palmatum, L . subareolatum , L . yunnanense and L . volubile have this type of surface ornamentation of spores. In type III, both the distal and equatorial areas of spores are coarsely verrucate, while the proximal area is smooth. L. dimorphum, L. digitatum and L. kingii have this type of surface ornamentation of spores. In type IV, the surface of spores is coarsely reticulate. L. scandens and L. reticulatum have this type of surface ornamentation of spores. The surface contours of the reticulate type (type IV) are formed by the exospore, while that of the other types (types I, II, III) are formed by the perispore. The surface ornamentation of spores seems to be stable within species and thus is of important value in the taxonomy of the genus Lygodium.     

Spore morphology of pteridophytes from China Ⅱ. Sinopteridaceae

Spores of 61 species and 6 varieties in 9 genera of the Sinopteridaceae were examined under scanning electron microscope (SEM). Based on surface ornamentation and other features, the spores of the Sinopteridaceae are divided into three types. In type Ⅰ , the exospore is smooth and the surface ornamentation, which is reticulate, cristate, echinate or rugate, is formed by the perispore. All the other genera of this family, except for Onychium and Cryptogramma, have this pattern of spores. In type Ⅱ, the surface ornamentation is formed by both perispore and exospore. This pattern is found only in Cryptogramma. In type Ⅲ, the perispore is thin and the surface ornamentation is formed by the exospore. Onychium is characterized by this type of spores. Those genera with spores of type Ⅰ of the Sinopteridaceae seem to be closely related to each other and should be natural members of this family. The systematic position of Cryptogramma and Onychium, with spores of type Ⅱ and type Ⅲ respectively, however, should be reconsidered. Aleuritopteris might be the mostprimitive member of the Sinopteridaceae from the evidence of spore morph     

Ultrastructural study of spore wall morphogenesis inOphioglossum thermale kom. var.nipponicum (Miyabe et Kudo) nishida

Spore wall morphogenesis ofOphioglossum thermale var.nipponicum was examined by transmission electron microscopy. The spore wall of this species consists of three layers: endospore, exospore, and perispore. The spore wall development begins at the tetrad stage. At first, the outer undulating lamellar layer of the exospore (Lo) is formed on the spore plasma membrane in advance of the inner accumulating lamellar layer (Li) of the exospore. Next, the homogeneous layer of the exospore (H) is deposited on the outer lamellar layer. Both lamellar layers may be derived from spore cytoplasm; and the homogeneous layer, from the tapetum. Then the endospore (EN) is formed. It may be derived from spore cytoplasm. The membranous perispore (PE), derived from the tapetum, covers the exospore surface as the final layer. Though the ornamentation of this species differs distinctly from that ofO. vulgatum, the results mentioned above are fundamentally in accordance with the data obtained fromO. vulgatum (Lugardon, 1971). Therefore, the pattern of spore wall morphogenesis appears to be very stable in the genusOphioglossum.     

朝鲜介蕨孢子周壁发育的研究

利用光镜、扫描电镜和透射电镜对朝鲜介蕨[Dryoathyrium coreanum(Christ)Tagawa=Lunathyrium coreanum(Christ)Ching]孢子周壁的发育规律进行了研究。结果表明,朝鲜介蕨孢子两侧对称,单裂缝,表面具粗大的脊状褶皱,褶皱形成网状或拟网状纹饰。孢壁包括内壁、外壁和周壁。孢子外壁表面光滑,在四分孢子时期就已发育成熟。四分孢子分离后,周壁开始形成,周壁来源于孢子囊的绒毡层,是由原质型绒毡层的残余物在外壁上沉积而成。成熟的周壁很厚,可分为外层和内层。周壁内有大的空腔,主要是由周壁外层向外隆起形成的,隆起进而形成了孢子的脊状褶皱和表面纹饰。     

Remarks on hereditary regulation of spore wall pattern in intra- and interspecific crosses of Athyrium

SCHNELLER, J. J., 1988. Remarks on hereditary regulation of spore wall pattern in intra-and interspecific crosses of Athyrium . Artificial crosses between Athyrium filix-femina subsp. angustum , subsp. cyclosorum , subsp. filix-femina with a rugulose perispore and A. filix-femina subsp. asplenioides with a folded rugulose perispore are investigated. In the sporangia of the F-l generation all the spores are of the same intermediate perispore pattern. This suggests a sporophytic regulation of the spore ornamentation and a codominant inheritance of the wall characters. Natural hybrids between diploid A. filix-femina with rugulose perispore and diploid A. distenlifolium with folded rugulose perispore are integrated in this study. The observations on spores of these hybrids showing different ploidy levels and different genetic combinations support the suggestion of a sporophytic regulation of spore ornamentation. The extent of folding changes gradually, depending on the occurrence and ratio of the genome of A. distenlifolium a result that is in agreement with the idea of a codominant inheritance.     

乌蕨孢子壁的形成和发育

利用光镜、扫描电镜和透射电镜对鳞始蕨科（Lindsaeaceae）乌蕨（Stenoloma chusanum Ching）孢壁的形成和发育进行了研究。结果表明乌蕨孢子两侧对称、单裂缝,表面具疣状纹饰。孢壁由内壁、外壁和周壁三部分构成。外壁在四分体阶段已基本形成,其表面光滑,质地均匀,由孢粉素形成。周壁是由绒毡层残余物在外壁表面沉积形成,可分为周壁内层、周壁中层和周壁外层三部分。在周壁中层与外层之间有一层均匀的空间。最后,本文探讨了孢壁的形成和发育规律,研究结果对揭示孢子纹饰和孢壁各层的形成过程、来源和稳定性有重要的意义,并为孢粉学和系统学研究提供基础资料。