丹东蒲公英专性无融合生殖特性

采用田间去雄套袋、花粉活性与花粉管萌发观测等交配系统实验,辅以染色体分析、胚囊发育观察以及流式细胞仪检测,对丹东蒲公英(Taraxacum antungense)生殖特性进行系统研究。结果表明,去雄套袋情况下,结籽率高达96%,由此证明交配系统具有极高的无融合发生率;自花授粉不能萌发,花粉活性仅为20.6%,异花授粉虽可萌发,但生长缓慢,花粉在到达子房前,花粉管已停止生长并消失;二分体时期,合子端大孢子发育为功能性大孢子,珠孔端大孢子退化消失,经蓼型发育,形成7细胞8核,卵细胞继续发育形成原胚,中央细胞形成胚乳,其它细胞退化消失,花未开放前,已形成球形胚。此外,丹东蒲公英为三倍体。流式细胞仪检测结果表明,丹东蒲公英为专性无融合生殖,胚乳自主发育。综合以上研究结果,说明丹东蒲公英具专性无融合生殖特性。     

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.     

入侵植物美洲商陆的传粉生态学特性

从开花物候、花朵数量性状、花粉活力、花粉组织化学、柱头可授性、花粉在柱头上的萌发状况、杂交指数、花粉胚珠比、传粉媒介以及繁育系统等方面,研究了外来入侵植物美洲商陆(Phytolacca americana)的传粉生态学特性,为揭示该物种成功入侵的机理提供依据.结果表明:美洲商陆种群花期可达45~70 d,单花花期为2~3d,可进一步分为杯状花期、花瓣平展期、花瓣下垂期、花瓣反卷期;花冠直径在下垂期最大且不超过1 cm,花药与柱头间距离在1 ~2.5 mm,有利于自交的发生;花瓣平展期与花瓣下垂期花粉活力差异显著(P<0.05),杯状花期与花瓣平展期花粉活力差异不显著(P>0.05),花瓣平展期花粉活力可达85%;雌蕊柱头可授性在花瓣平展期最强;杯状花期合生柱头开裂,花瓣平展期柱头9~ 10裂,接受花粉的表面积增大;花药散粉时间与合生柱头开裂时间相吻合,有助于柱头接受花粉;扫描电镜下观察到花粉在花瓣平展期的柱头上已萌发;每朵花可提供1667~3222粒花粉,胚珠9~10个,花粉胚珠比(P/O)为340.88±34.99,表现为兼性自交;美洲商陆杂交指数(OCI)为3,花粉粒属于含脂型,主要传粉昆虫有蜜蜂、胡蜂、食蚜蝇、细腰蜂.综上所述,美洲商陆自交亲和,花粉活力高、柱头可授性强,且高花粉活力与强柱头可授性出现在相同的时期,增加了花粉落置柱头及在柱头上萌发的几率;虫媒花,访花者行为与花朵相适应,有利于提高坐果率,这样的繁殖机制与传粉特点是美洲商陆成功入侵的主要因素之一.     

新牧Ⅰ号杂花苜蓿异交机制与自花粉的生殖干扰

通过控制试验和荧光观测等手段对新牧Ⅰ号杂花苜蓿Medicago varia Martyn'Xinmu No.1'柱头可授期与最佳授粉时间、自花粉的堵塞效应、花粉萌发与花粉管生长状况等进行研究,结果显示:(1)苜蓿柱头可授期与单花寿命具高度的同步性,在单花开放的第1天授粉,传粉效率最高,结果率达65.170%±2.01%(P<0.01),为柱头的最佳授粉时期;在单花开放后第4天授粉,其结果率仍达34.25%±6.73%.(2)自花授粉比异花授粉有着较低的花粉萌发率和花粉管生长速度;清除柱头自花粉后再授异花粉,其结荚率/花序和英内种子粒数由原来的51.760%±5.37%和2.11±0.18粒,提高到72.31%±6.24%(P<0.01)和3.46±0.25粒(P<0.01),自花粉对柱头的堵塞效应非常明显.(3)在繁育系统中,苜蓿采取了雌雄异熟和自交不亲和两套机制来避免自交,但是由于其独特的花结构,即使雄蕊先熟,在保证苜蓿异交机制中也没有起到有效的作用,而其典型的自交不亲和系统,虽然保证了苜蓿较低的自交率,却无法避免自花粉的生殖干扰.     

七叶树花粉活力和柱头可授性变化的研究

采用花粉离体萌发法研究不同蔗糖浓度、硼酸浓度和不同温度对七叶树花粉萌发的影响及花粉活力测定,用联苯胺-过氧化氢法测定柱头可授性.结果表明:七叶树花粉萌发的最佳培养基是12％蔗糖+30 mg/L硼酸,花粉萌发的最适温度为25℃.雄花在开花当天花粉活力最高达75.69％,并在开花当天的上午10:00时,花粉活力最强,10:00～16:00花粉活力保持较高活力,是最佳授粉时段.两性花的柱头可授期持续时间较长,为8～9 d,开花3d达到最强,开花1～4 d柱头可授性保持较高水平,为授粉的最佳时间段.因此,从七叶树的花部特征、花粉活力与柱头可授性及花粉萌发的条件看,在长期的自然选择下七叶树在花部结构和开花生理上都是相配合的,以保障生殖成功.     

宁夏枸杞传粉生态学初步研究

田间观察检测了宁夏枸杞(Lycium barbarum L.)9个品系的开花物候、开花动态、花粉活力、柱头可授性及其繁育系统,并对花粉萌发、花粉管生长以及访花者的种类和访花行为进行了初步研究.结果表明,宁夏枸杞整个居群有长达5个月的花期,单花的花期仅为3～4 d,花粉活力可保持15 d左右,柱头可授性在72 h左右,雌雄生殖单位在持续时间上有较长的相遇期;花粉数量与胚珠比(P/O)为4 000左右,杂交指数(OCI)介于3或4,繁育系统为异交型,需要传粉者;荧光显微观察表明,参试的3个品系的花粉均能在柱头上萌发,2个有自交不亲和现象,其位置发生在花柱的上半部分和子房内.访花昆虫有17种,分属双翅目、膜翅目和鳞翅目,花的结构和开花式样适合以意大利蜜蜂和食蚜蝇为主的多种昆虫传粉.     

膏桐花粉活力与柱头可授性及其生殖特性研究

采用TTC法测定了膏桐花粉的活力和寿命,用联苯胺-过氧化氢法测定其柱头可授期,以套袋结果检测花粉活力与柱头可授性的变化,以研究柱头颜色变化与柱头可授性的关系以及开花式样对生殖成功的影响.结果表明:(1)膏桐雄花单花花期一般为2 d,花后0~9 h内花粉活力相对较高,24~33 h后花粉活力较低,48 h后花粉基本无活力.(2)膏桐雌花单花期为5~12 d,柱头可授性在花后1~4 d最强,5~8 d可授性开始逐渐降低,第9天基本失去可授性.(3)膏桐柱头表面无明显的渗出物,柱头的可授性与柱头颜色的变化相关,柱头绿色越多,柱头可授性越强;遇降雨时,少量雌花的花瓣展开而柱头仍呈球状,或者花瓣不展开而柱头先伸出,此时柱头可授性较差.(4)膏桐常表现为雄性先熟,尽管雌花数目较少,但开放速率较快,且集中在第3~5天开放,雌花开放完毕也仍有雄花未开放,为展开后的柱头留有较长时间等候昆虫传送花粉,为保障生殖成功提供了机会,但少数花序先开雌花,后开雄花,有支持异交而降低自交的倾向.     

光果甘草生殖生物学特性的初步研究

对光果甘草的花部特征、花粉活力、柱头可授性和花粉-胚珠比(P/O)进行了初步研究.结果表明:(1)光果甘草雄蕊异型,雌雄蕊异位,有利于避免自花授粉;(2)开花当天花粉活力在上午12:00最高,为91.8%,14:00迅速下降,16:00到达最低,16:00以后逐渐上升;(3)柱头可授性可持续4 d,以开花当天可授性最强;(4)花粉-胚珠比(P/O)为1 751.1±217.002,表明其繁育系统类型为兼性异交.     

楸树的开花生物学及繁育系统研究

本文对楸树的开花习性进行观察记录,从花粉生活力、柱头可授性及套袋实验等方面对楸树的传粉机制进行研究。结果表明,楸树为典型的雌雄同花植物,花冠张开后,雌蕊柱头二裂开始张开,具有可授性,且张开120°时可授性最强;雌蕊柱头在张开期间具有较高生活力,花冠脱落后生活力开始下降,楸树单花花粉量大,可达9.4×106;楸树自交不亲和,不存在无融合生殖现象,且人工异花授粉坐果率高达94%。通过对楸树花器官的形态学及传粉的研究,为楸树的繁殖效率及其杂交育种研究奠定基础。     

簇枝补血草花的二态性及繁育系统研究

白花丹科被列为异型花柱较多的科,该文以补血草属簇枝补血草为材料,通过对野外居群的花部特征、花期物候和繁育系统等研究,探讨花部形态多态性及其对生殖的影响。簇枝补血草具有两种类型植株,具玉米状柱头和A型花粉的植株称为C型植株;具乳头状柱头和B型花粉的植株称为P型植株,且A/B型花粉的大小、外壁纹饰不同。单花发育过程中两型植株的花萼、雌蕊大小差异明显,随着花的成熟差异逐渐消失。两型植株都为雌蕊高于雄蕊,柱头探出式雌雄异位;C型植株的花期较P型植株长约2 d。一天当中,A型花粉活力高峰期为13:00,B型花粉在11:00和15:00都表现为高峰期;玉米状柱头可授性最强时期在13:00～15:00,乳头状柱头则在15:00。两型花粉可育性在盛花期最高,终花期时B型花粉可育性明显高于A型。荧光染色观察发现花粉萌发和花粉管的生长速度都为:异型授粉＞同型授粉,B型花粉在乳头状柱头上不能完成受精。此外,人工授粉实验也表明异型授粉结实率显著高于同型,P型植株经同型授粉结实现象并不明显,存在少量无融合生殖。研究表明簇枝补血草花部具二态性,繁育系统为兼性异交,其中乳头状柱头对A型花粉亲和,对B型花粉不亲和,但玉米状柱头却对A/B型花粉都亲和,这打破了该科的异型自交不亲和的例证。     

The effect of temperature on stigmatic receptivity in sweet cherry (Prunus avium L.)

Plant reproduction is highly vulnerable to environmental conditions such as temperature and, consequently, planet warming may have significant consequences on the reproductive phase with serious implication in agricultural crops. Although pollen tube growth is clearly affected by temperature, little information is available on its effect on the female side and on flower receptivity. In this work, the effect of temperature has been evaluated on stigmatic receptivity of sweet cherry in vivo, in the laboratory, and in planta, in the field. Results herein show that temperature has a clear effect on the duration of stigmatic receptivity. Thus, whereas high temperature reduced stigmatic receptivity, low temperature enlarged it. The stigma lost the capacity to offer support first for pollen penetration, second for pollen germination and, finally, for pollen adhesion. The effect of temperature was more pronounced on pollen germination and penetration than on pollen adhesion. High temperature reduced the germination capacity of the pollen as early as the first day after anthesis, a time when no apparent signs of stigma degeneration are apparent. This clear effect of temperature on stigmatic receptivity and pollen performance may have clear implication in crop performance and in establishing screening criteria of best‐adapted genotypes.     

Arabinogalactan-protein secretion is associated with the acquisition of stigmatic receptivity in the apple flower

Background and Aims

Stigmatic receptivity plays a clear role in pollination dynamics; however, little is known about the factors that confer to a stigma the competence to be receptive for the germination of pollen grains. In this work, a developmental approach is used to evaluate the acquisition of stigmatic receptivity and its relationship with a possible change in arabinogalactan-proteins (AGPs).

Methods

Flowers of the domestic apple, Malus × domestica, were assessed for their capacity to support pollen germination at different developmental stages. Stigmas from these same stages were characterized morphologically and different AGP epitopes detected by immunocytochemistry.

Key Results

Acquisition of stigmatic receptivity and the secretion of classical AGPs from stigmatic cells occurred concurrently and following the same spatial distribution. While in unpollinated stigmas AGPs appeared unaltered, in cross-pollinated stigmas AGPs epitopes vanished as pollen tubes passed by.

Conclusions

The concurrent secretion of AGPs with the acquisition of stigmatic receptivity, together with the differential response in unpollinated and cross-pollinated pistils point out a role of AGPs in supporting pollen tube germination and strongly suggest that secretion of AGPs is associated with the acquisition of stigma receptivity.Key words: AGPs, arabinogalactan proteins, apple, Malus × domestica, pollen, pollen tube, stigma, stigmatic receptivity, flower receptivity     

Asynchronous development of stigmatic receptivity in the pear (Pyrus communis; Rosaceae) flower

While stigma anatomy is well documented for a good number of species, little information is available on the acquisition and cessation of stigmatic receptivity. The aim of this work is to characterize the development of stigma receptivity, from anthesis to stigma degeneration, in the pentacarpellar pear (Pyrus communis) flower. Stigma development and stigmatic receptivity were monitored over two consecutive years, as the capacity of the stigmas to offer support for pollen germination and pollen tube growth. In an experiment where hand pollinations were delayed for specified times after anthesis, three different stigmatic developmental stages could be observed: (1) immature stigmas, which allow pollen adhesion but not hydration; (2) receptive stigmas, which allow proper pollen hydration and germination; and (3) degenerated stigmas, in which pollen hydrates and germinates properly, but pollen tube growth is impaired soon after germination. This developmental characterization showed that stigmas in different developmental stages coexist within a flower and that the acquisition and cessation of stigmatic receptivity by each carpel occur in a sequential manner. In this way, while the duration of stigmatic receptivity for each carpel is rather short, the flower has an expanded receptive period. This asynchronous period of receptivity for the different stigmas of a single flower is discussed as a strategy that could serve to maximize pollination resources under unreliable pollination conditions.     

Papillar integrity as an indicator of stigmatic receptivity in kiwifruit (Actinidia deliciosa)

Stigmatic receptivity is a major factor limiting fruit set inkiwifruit (Actinidia deliciosa). The aim of this work was toknow what determines the cessation of stigmatic receptivityin this species. Stigmatic receptivity has been analysed inkiwifruit through the capacity of the stigma to sustain pollengermination and has been related to stigmatic development anddegeneration.The stigma of kiwifruit flowers has a papillatesurface which from anthesis is covered with an abundant exudate.Papillae are unicellular and contain a number of phenolic deposits.During the lifetime of the flower these papillae gradually loseturgidity, while stigmatic secretion increases until 5 d afteranthesis when papillae start rupturing and the papillar contentis liberated into the germination medium. Stigmatic receptivityis high at anthesis and lasts for the next 4 d. However, itdrastically decreases 5 d after anthesis and it is nil 2 d later.The pattern of stigmatic receptivity closely fits that of papillarintegrity, indicating that stigmatic receptivity relies on thisintegrity. Since papillar integrity can easily be evaluatedin stigmatic arms, this criterion can be used as a quick methodto estimate stigmatic receptivity. Key words: Actinidia deliciosa, kiwifruit, stigma, receptivity, pollen     

Self-incompatibility and the pollen-stigma interaction inTradescantia ohiensis rafin

Summary Self-incompatibility (SI) is reported for an accession ofTradescantia ohiensis. Pollen tube inhibition is stigmatic. The stigma is wet and papillate, the papillr surface bearing conspicuous blebs particularly in the mid- and basal regions of the cell. A proteinaceous pellicle is present on the surface of the papillar cuticle. The penetration of the stains calcofluor white and alcian blue into the cell wall of fresh stigma papillae strongly indicates that the permeability of the papillae is greatest at the mid-region of the cell and not at the tip. When single pollen grains are attached to the tip of a papilla there is either no response at all or the pollen adheres to the papilla. When attached in the mid-region pollen adheres, and often germinates. It is concluded that the sites of pollen receptivity are the mid- and basal regions of the papular cell.     

Stigma-surface Esterase Activity and Stigma Receptivity in Some Taxa Characterized by Wet Stigmas

Stigma-surface esterase activity and stigma receptivity througha sequence of developmental stages of the pistil have been studiedin four taxa characterized by having wet stigmas — Petuniahybrida, Nicotiana tabacum, Crinum defixum and Amaryllis vittata.The style is solid in the first two and hollow in the lattertwo taxa. In all the taxa, stigma—surface esterase couldbe detected in a thin surface layer (pellicle) from a very earlystage of pistil development, irrespective of the presence orabsence of the exudate. However, the taxa showed variation instigma receptivity. In Petunia and Nicotiana, stigmas from pistilsof all the stages supported pollen germination and tube growth.In Amaryllis and Crinum, stigmas of only the mature pistils,when the exudate is present on the stigma, supported normalpollen germination and tube growth. It is inferred that in taxacharacterized by a wet stigma and solid style, the factors requiredfor pollen germination are present from an early stage of pistildevelopment and the exudate per se is not involved in pollengermination. In taxa characterized by a wet stigma and hollowstyle, however, the pellicle does not carry the factors requiredfor pollen germination and tube growth; they appear to be presentin the exudate. Petunia hybrida Vilm, Nicotiana tabacum L., Crinum defixum, Ker-Gawl, Amaryllis vittata Ait., tobacco, pollination, pollen germination, stigmatic exudate, stigma receptivity, stigma-surface esterase, esterase activity     

Regulation of seed number and female incitation of mate competition by a pH-dependent proteinaceous inhibitor of pollen grain germination in Leucaena leucocephala

Summary Leucaena leucocephala generally produces pods with more than 7–9 seeds. This is regulated by the stigmatic inhibition of pollen grain germination when the pollen grains are less than a critical number in the stigma. This number-dependent inhibition of pollen grain germination is effected by a pH-dependent proteinaceous inhibitor active at the stigmatic pH. Only when the pollen grains in the stigma exceed the critical number, they inactivate the inhibitor by collectively raising the stigmatic pH and thus overcoming the inhibition. The adaptive significance of such pre-fertilization mechanism for the female in inciting mate competition among the pollen grains is discussed. The evolution of en masse pollen grain dispersal units is explained as a sexual selection strategy by males in response to such stigmatic inhibition by females.     

Different regulatory processes control pollen hydration and germination in Arabidopsis

To elucidate the functional differences in how Arabidopsis stigmas regulate pollen hydration and germination, we analyzed receptivity of stigmas, epidermal surfaces (leaves, stems of inflorescence bolts, and floral organs), and an abiotic surface (cover glass) for pollen hydration and germination. Using 65% relative humidity (RH), we found that mature pollen grains were able to hydrate and germinate on stigmas at flower developmental stages 9–13, but not on the distal end of pistils at stage 8, epidermal surfaces, or glass. Furthermore, under 100% RH, pollen grains could hydrate on all tested surfaces, but pollen germination was observed only on the young floral organs (stages 9–12) and the stigmas at stages 9–13. The distal ends of pistils at stage 8, the epidermal surfaces, and the cover glass did not support pollen germination even under 100% RH. Our results indicate that pistil factors regulating pollen hydration and germination are synthesized at stage 9 when stigmatic papillar cells begin to develop. Although pistil factors involved in pollen hydration may only be present on the stigma, the factors involved in pollen germination may localize on both the stigma and surfaces of unopened floral organs.     

Stigma development and receptivity in almond (Prunus dulcis)

BACKGROUND AND AIMS: Fertilization is essential in almond production, and pollination can be limiting in production areas. This study investigated stigma receptivity under defined developmental stages to clarify the relationship between stigma morphology, pollen germination, tube growth and fruit set. METHODS: Light and scanning electron microscopy were employed to examine stigma development at seven stages of flower development ranging from buds that were swollen to flowers in which petals were abscising. Flowers at different stages were hand pollinated and pollen germination and tube growth assessed. Artificial pollinations in the field were conducted to determine the effect of flower age on fruit set. KEY RESULTS: Later stages of flower development exhibited greater stigma receptivity, i.e. higher percentages of pollen germination and more extensive tube growth occurred in older (those opened to the flat petal stage or exhibiting petal fall) than younger flowers. Enhanced stigma receptivity was associated with elongation of stigmatic papillae and increased amounts of stigmatic exudate that inundated papillae at later developmental stages. Field pollinations indicated that the stigma was still receptive and nut set was maintained in older flowers. CONCLUSIONS: Stigma receptivity in almond does not become optimal until flowers are past the fully open stage. The stigma is still receptive and fruit set is maintained in flowers even at the stage when petals are abscising. Strategies to enhance pollination and crop yield, including the timing and placement of honey bees, should consider the effectiveness of developmentally advanced flowers.     

POLLINATION IN LUPINUS NANUS SUBSP. LATIFOLIUS (LEGUMINOSAE)

Floral morphology and phenology and the timing of stigmatic receptivity and pollen viability were studied to elucidate the mechanisms by which self-pollination in Lupinus nanus subsp. latifolius is minimized under natural conditions. Pollen germination and pollen tube growth suggest that a physiological self-incompatibility system does not exist. Instead, self-pollination is minimized by protandry and by a collar of peristigmatic hairs, which initially inhibit access of autologous pollen to the stigma. These hairs subsequently wilt, permitting self-pollination of unvisited flowers. Pollen germinates in vivo one day before substantial metabolic enzyme activity can be detected. Citric acid cycle enzymes are not detectable in pollen, but those of anaerobic metabolism are. Beginning on the second day postanthesis, stigmatic secretions exude from weak areas on lateral walls of the elongate epidermal papillae, welling up in the interstices between these cells. This contrasts with the stigmas of other papilionoid legumes, in which secretions accumulate beneath the cuticle covering the stigmatic cells, and the often-thin cuticle must be ruptured before pollen and exudate can come into contact.