6种铁线莲属植物的柱头特征对传粉的适应

为了解传粉过程中柱头对花粉的捕获策略,对6种铁线莲属植物（甘青铁线莲、灌木铁线莲、粉绿铁线莲、薄叶铁线莲、粗齿铁线莲和短尾铁线莲）的柱头显微结构进行扫描电镜观察,发现6种铁线莲属植物的柱头均位于花柱的腹缝面,由花柱腹缝两侧细胞发育成柱头乳突,乳突形状随花期逐步从球状到指状甚至长指状过度,并伴随着柱头受粉面从花柱顶端朝花柱基部渐次发育成熟的特殊发育式样。观察分析6种铁线莲的花部综合征及花粉胚珠比（P/O）发现,柱头的此类发育式样与其他花部构成存在功能上的协同一致。为理解铁线莲属植物花部的进化提供了新的思路和视野,对观赏用铁线莲属植物的育种栽培具参考价值。     

驴蹄草属和金莲花属(毛茛科)花器官的形态发生及系统学意义

利用扫描电镜观察了驴蹄草Caltha palustris L.和川陕金莲花Trollius buddae Schipcz.花器官的发生和发育过程。结果显示:驴蹄草和川陕金莲花的所有花器官均螺旋状向心式发生、向心式发育,花器官的螺旋状发生方式在毛茛科Ranunculaceae可能是一种基本式样;苞片、萼片与其他花器官原基的形状明显不同,显示苞片、萼片与其他花器官在系统发生上有所不同;川陕金莲花的花瓣在早期延迟发育且基部具囊,花瓣的延迟发育在毛茛科具花瓣的属中非常普遍,而花瓣基部的囊类似于耧斗菜属Aquilegia一些植物;两个属雄蕊群一纵列雄蕊中的小孢子均向心式发育,这种发育方式在毛茛科可能为基本类型。两个属植物的心皮原基均为对折式,在发育过程中,驴蹄草心皮顶端沿腹缝线形成下延的柱头组织,川陕金莲花不形成明显的柱头组织。根据花形态发生和发育特点,并结合其他研究成果,认为这两个属不应当属于同一个族。     

耧斗菜属花部形态发生

用扫描电镜观察了无距耧斗菜（Ａｑｕｉｌｅｇｉａ ｅｃａｌｃａｒａｔａ Ｍａｘｉｍ ．）和北美耧斗菜（Ａ． ｃａｅｒｕｌｅａＪａｍ ｅｓ．）雄蕊群和雌蕊群的发生过程,并在光学显微镜下检查了同一雄蕊群不同轮雄蕊小孢子发育的顺序． 发现耧斗菜属雄蕊群的发生是向心发生,而小孢子发育和花药成熟顺序是离心的． 说明该属雄蕊群离心发育是次生现象;它在不同类群中出现,可能具有平行演化的性质,其系统学价值尚需重新评价     

欧报春二型花柱的繁育特性研究

二型花柱植物通常具有自交不亲和性,在不同植物中所表现的可育性不同。欧报春(Primula vulgaris)是典型的二型花柱植物,为了探究欧报春的繁育特性,通过温室栽培,对欧报春的长花柱和短花柱的花部特征、花粉和花柱形态、花粉活力、柱头可授性、花粉/胚珠比、杂交指数、杂交亲和性、花粉管观察进行研究。结果表明,(1)长花柱和短花柱的花冠直径、花冠筒长度、柱头高度、花药高度和花筒中部直径均表现出两型性;(2)花粉和柱头观察发现花粉极轴长、花粉赤道轴长、花柱直径、柱头乳突细胞和花粉数量均有差异;(3)长花柱的花粉/胚珠比为384.20,短花柱为369.70,属于兼性异交类型;长花柱和短花柱的花粉活力和柱头可授性能在较长时间内维持较高活力;(4)长花柱杂交指数值为5,短花柱为4,表明繁育系统类型为异交,部分自交亲和,需要传粉者;6种授粉组合均能结实,异型花间授粉的结实数明显高于同型自花授粉和异株同型授粉;短花柱为母本的异型花间授粉组合亲和性优于其他组合;欧报春存在自交不亲和性,长花柱的自交不亲和性低于短花柱。     

青篱柴通过促进亲和花粉生长而提高传粉精确性

异型花柱植物的适应意义在于提高亲和花粉的传递, 从而促进异交, 但是有不少研究发现柱头上落置了大量不亲和花粉。目前, 很少有人研究柱头是否有利于亲和花粉的萌发和花粉管伸长, 以及通过去雄处理排除花内和植株内不亲和花粉干扰从而验证二型花柱植物是否可以促进异交。本研究以亚麻科青篱柴属(Tirpitzia)的二型花柱植物青篱柴(T. sinensis)为研究对象, 分居群调查了青篱柴长、短柱型的植株数量, 测量不同柱型的花粉与柱头大小以及观察其表面纹饰, 测定不同开花时间长、短柱型的柱头活性与花粉活力, 统计自然状态下柱头上落置的不同表型花粉比例, 进一步统计花内、株内去雄和自然对照下柱头上落置的不同表型花粉比例, 计算型间、型内和混合授粉花粉管长度和花粉萌发率, 人工授粉检测其是否型内异交不亲和与自交不亲和。结果表明, 自然居群中长、短柱型青篱柴植株数量没有显著性差异; 短柱型青篱柴花粉体积显著大于长柱型, 且二者花粉表面纹饰不同, 但不同柱型的柱头表面积与表面纹饰无差异; 青篱柴开花第一天的花粉活力显著高于开花第二天, 而柱头活性在开花前两天无显著性差异; 自然状态下柱头上落置的不亲和花粉比例显著高于亲和花粉; 在长柱型青篱柴中, 花内和株内去雄显著提高了柱头上亲和花粉的落置比例; 柱头上授型内花粉, 其花粉萌发率和花粉管的长度都显著低于授型间花粉; 授粉结果表明青篱柴为型内异交不亲和与自交不亲和。二型花柱植物通过促进亲和花粉的萌发和花粉管的伸长而有利于型间授粉, 从而显著提高其传粉精确性。     

花粉—雌蕊相互作用的控制机理

本文介绍了近年来在花粉—雌蕊相互作用的控制机理及发育调控中取得的一些进展。花粉与雌蕊的识别由一系列不亲和基因所控制的专一性糖蛋白所介导。在花成熟后期这些基因开始表达,合成大量的S蛋白质,从而植物获得自交不亲和的特性。雌蕊S蛋白质位于柱头或花柱中,它们能抑制自交不亲和花粉管生长。     

长花柱型滇丁香小孢子发生及雄配子体发育

利用常规石蜡切片法和细胞学压片法,对异型花柱植物滇丁香的长花柱型植株的小孢子发生、雄配子体发育及花粉萌发进行观察。结果表明:(1)长花柱型滇丁香具5枚花药,花药4室。(2)花药壁由1层表皮、1层花药内壁、2层中层和1~3层绒毡层组成;花药壁发育方式为基本型,绒毡层类型为腺质绒毡层。(3)小孢子母细胞减数分裂的胞质分裂为同时型,四分体排列方式为四面体型,偶有左右对称型;不同药室间小孢子母细胞减数分裂不同步。(4)成熟花粉粒为二细胞型。(5)小孢子发生和雄配子体发育过程正常,表明长花柱型滇丁香属于发育正常的两性花。(6)授粉4h后,长花柱型滇丁香的花粉在长、短两种花柱柱头上的萌发率分别达(91.8±1.6)%和(93.2±1.1)%,且两者间无显著性差异(t=1.585,df=8,p=0.152),表明长花柱型滇丁香的成熟花粉粒在长、短两种花柱柱头上的萌发均正常。     

耧斗菜属长果耧斗菜在陕西省的新分布

该文报道了耧斗菜属植物长果耧斗菜(Aquilegia yangii Y. LuoL. Li)的新分布区——陕西省凤县通天河国家森林公园,将该种的分布区向东扩展到了陕西省的秦岭地区,丰富了陕西省新增植物分布记录,为秦岭地区的物种多样性研究提供了证据。     

灰枣开花生物学特性研究

通过田间定位观察、MTT检测和扫描电镜观察等方法对灰枣的开花生物学特性进行了观察,探讨其生殖成功基础.结果表明:(1)灰枣单花寿命约33 h;(2)灰枣花粉胚珠比为15 196±4 290;(3)花粉活力在散粉后7 d内相对较高,12 d后所有花粉丧失活性;(4)从蕾裂期到花瓣雄蕊分离期雌蕊两心皮聚拢,此后在花瓣展平期柱头开始分离,柱头在分离后开始具有强可授性;(5)花柱分离后,位于腹缝线两侧的细胞也发育成柱头乳突,从而增加了可接受花粉的面积;(6)花药散粉早于柱头可授期,花粉不能自发落置在柱头上,表现出雌雄异熟和雌雄空间异位的花部特征.     

芥菜型油菜与白菜正反杂交的胚胎学研究

利用荧光技术对芥菜型油菜(Brassica juncea)与白菜(B. pekinesis)种间正反杂交后花粉萌发和花粉管生长过程进行了观察。结果显示: 芥菜型油菜与白菜正交授粉后, 花粉在柱头上能正常萌发, 多数花粉管沿花柱到达胚珠完成受精, 且受精方式有珠孔受精、合点受精和中部受精, 少量花粉管生长不正常, 出现花粉管顶端膨大扭曲, 花粉管分支等异常现象; 反交授粉后, 花粉在柱头上萌发时柱头乳突细胞产生强烈胼胝质反应, 影响花粉管生长, 只有少量花粉管通过花柱到达胚珠完成受精。用石蜡切片技术观察了正反杂交后杂种的胚胎发育, 正交杂种胚胎发育较早, 胚和胚乳生长较正常, 杂种胚一般均能发育至成熟; 反交杂种胚发育至心型期便不能继续发育, 胚乳也停滞在游离核阶段并最终败育。综合分析 表明, 芥菜型油菜与白菜正反杂交都存在一定程度的受精不亲和性。     

Stigma/style cell cycle inhibitor 1 (SCI1), a tissue-specific cell cycle regulator that controls upper pistil development

A cDNA encoding a small lysine-rich protein of unknown function was identified in a tobacco (Nicotiana tabacum) stigma/style suppression subtractive hybridization cDNA library. After its characterization, the corresponding gene was designated stigma/style cell cycle inhibitor 1 (SCI1). Fluorescence microscopy with an SCI1-GFP protein fusion demonstrated its nuclear localization, which was confined to the interchromatic region. Real-time RT-PCR and in situ hybridization experiments showed that SCI1 is stigma/style-specific and developmentally regulated. SCI1 RNAi knockdown and overexpression plants had stigmas/styles with remarkably enlarged and reduced areas, respectively, which was attributable to differences in cell numbers. These results indicate that SCI1 is a tissue-specific negative cell cycle regulator. The differences in cell division had an effect on the timing of the differentiation of the stigmatic papillar cells, suggesting that their differentiation is coupled to stigma cell divisions. This is consistent with a role for SCI1 in triggering differentiation through cell proliferation control. Our results revealed that SCI1 is a novel tissue-specific gene that controls cell proliferation/differentiation, probably as a component of a developmental signal transduction pathway.     

Floral morphogenesis of Caltha and Trollius (Ranunculaceae) and its systematic significance

The floral morphogenesis of Caltha palustris L. and Trollius buddae Schipcz. was observed with a scanning electron microscope (SEM). The primordia of all floral organs initiate spirally and centripetally and develop centripetally. The spiral initiation sequence may be a basic pattern in Ranunculaceae. The primordia of bracts, sepals, and other floral organs are different in shape: the bract primordia are triangle, the sepal primordia crescent, and the petal (in Trollius), stamen, and carpel primordia hemispheric. This may indicate that the bracts, the sepals and other floral organs are different in origin. The petals are retarded in early developmental stages in Trollius buddae Schipcz, and have purses at the base. The retarded petals are very common in Ranunculaceae and the purse of the petal is similar to that of some Aquilegia species. The microspores in a longitudinal series of stamens develop centripetally in Caltha and Trollius; this may be a basic pattern in Ranunculaceae. The carpel primordia are plicate. In the developmental process of the carpels, the stigmatic tissue appears from the apex of the style and is decurrent along the ventral suture in Caltha, but there is no obvious stigmatic tissue in Trollius. Based on floral morphogenesis characteristics as well as the results from molecular systematics, comparative morphology and palynology studies, we consider that Caltha is not closely related to Trollius and that these two genera should not be treated in the same tribe.     

Characterization of Aquilegia Polycomb Repressive Complex 2 homologs reveals absence of imprinting

Epigenetic regulation is important for maintaining gene expression patterns in multicellular organisms. The Polycomb Group (PcG) proteins form several complexes with important and deeply conserved epigenetic functions in both the plant and animal kingdoms. The plant Polycomb Repressive Complex 2 (PRC2) contains four core proteins, Enhancer of Zeste (E(z)), Suppressor of Zeste 12 (Su(z)12), Extra Sex Combs (ESC), and Multicopy Suppressor of IRA 1 (MSI1), and functions in many developmental transitions. In some plant species, including rice and Arabidopsis, duplications in the core PRC2 proteins allow the formation of PRC2s with distinct developmental functions. In addition, members of the plant specific VEL PHD family have been shown to associate with the PRC2 complex in Arabidopsis and may play a role in targeting the PRC2 to specific loci. Here we examine the evolution and expression of the PRC2 and VEL PHD families in Aquilegia, a member of the lower eudicot order Ranunculales and an emerging model for the investigation of plant ecology, evolution and developmental genetics. We find that Aquilegia has a relatively simple PRC2 with only one homolog of Su(z)12, ESC and MSI1 and two ancient copies of E(z), AqSWN and AqCLF. Aquilegia has four members of the VEL PHD family, three of which appear to be closely related to Arabidopsis proteins known to associate with the PRC2. The PRC2 and VEL PHD family proteins are expressed at a relatively constant level throughout Aquilegia vulgaris development, with the VEL PHD family and MSI1 expressed at higher levels during and after vernalization and in the inflorescence. Both AqSWN and AqCLF are expressed in Aquilegia endosperm but neither copy is imprinted.     

滇鼠刺花的形态发生（鼠刺科）

在扫描电镜下 ,观察了滇鼠刺 (IteayunnanensisFranch .)花的形态发生。花 3朵一束 ,排成总状花序。花器官为轮状结构 ,向心发生 ;花萼以 2 /5螺旋式相继发生 ,5个花瓣原基几乎同步地在花萼内侧与其互生的位置发生。雄蕊单轮对萼。当雄蕊发生后 ,花顶中心的分生组织开始凹陷 ,成为浅锅状 ;在其周围出现一个环状的分生组织 ,随之 ,2心皮原基产生 ,进而发育为马蹄形。初期的心皮相互分离 ,随着进一步发育 ,心皮内卷 ,彼此靠近、紧贴 ,逐渐于腹面合生 ,形成 2室的中轴胎座 ;花柱的腹维管束通过薄壁组织连通 ;花期柱头融合 ,因此该种为合生心皮。对鼠刺属 (Itea)及相关类群花发育性状和花结构进行了比较 ,支持把鼠刺属提升为鼠刺科 (Iteaceae)的观点。     

桦木科植物花柱适应风媒传粉的特征

植物体为适应自己的传粉系统, 表现出高度的适应特征。风媒花植物为适应风传播花粉, 要形成特殊的结构, 以扩大接受花粉粒的面积。利用扫描电镜观察了桦木科(Betulaceae)6属18种植物花柱的形态及花粉粒在花柱上的萌发过程, 探讨了桦木科植物花柱适应风媒传粉的特征。结果表明, 桦木科植物的二心皮(铁木、云南鹅耳枥稀为三心皮)雌蕊具柱状花柱, 柱头不发达, 花柱表皮细胞长条状, 纵向排列紧密。传粉时, 花柱表皮细胞能执行柱头的功能, 接受花粉粒, 为花粉粒萌发提供场所和萌发条件。桦木科植物花柱有2种类型: 一种是花柱表皮细胞能形成乳突, 花粉管经乳突细胞进入花柱; 另一种是花柱表皮细胞不形成乳突, 花粉管经过花柱表皮细胞或胞间隙进入花柱。无论花柱表皮细胞是否形成乳突, 乳突的形态、大小以及花粉管和乳突的结合方式等在族间、属间、属内种间存在差异。与基部被子植物相比, 桦木科植物的花柱呈现适应风媒传粉的进化特征。桦木科植物花柱表皮细胞形成的乳突与基部被子植物柱头乳突功能相同, 是桦木科植物风媒传粉的适应策略。     

The morphology of styles and stigmas inVicia (Leguminosae), and its systematic implications

The morphology and development of styles and stigmas ofVicia, one of the five genera of tribe Vicieae, were studied by scanning electron microscopy to contribute to a revision of infrageneric classification. Among the 22 species examined, variations were found as to: (1) whether a boundary between stigma and style is V-shaped when viewed from the adaxial side or not; (2) whether stylar hairs sprout on all sides of the style or only on the abaxial side; (3) whether a hairy area of the style connects with the stigma area first at lateral sides or at an adaxial side; (4) whether styles are tapered or bottle-neck-shaped; (5) whether styles are straight or bend abaxially. Based on these variations, five morphological types of styles and stigmas were provided with a diagnostic key. Comparisons with related tribes Cicereae, Coronilleae, Galegeae, Hedysareae, Loteae and Trifolieae as possible outgroups suggested that the V-shaped boundary between stigma and style is a synapomorphy of some species withinVicia, and that a dorsally compressed and abaxially tufted style, which was distributed in separate subgenera and sections sensu Kupicha but is now known to occur together with the V-shaped boundary, has evolved only one time in the genus, rather than more than once as supposed earlier.