宁夏枸杞的花粉呈现式样及交配系统研究北大核心CSCD

被子植物的花回馈、雌雄蕊时空分离特征和花粉呈现式样等花部特征及传粉者效率会影响雄性适合度和有性繁殖过程。宁夏枸杞(Lycium barbarum)是中国宁夏、新疆、内蒙等干旱和半干旱地区分布的特有种。该研究对新疆喀什地区宁夏枸杞自然种群的花部综合征、花粉呈现式样、花回馈、传粉者行为与交配方式的关系进行观察及统计分析,以探讨其花粉逐步呈现的适应性及其在提高雌雄繁殖过程中的意义。结果表明:(1)宁夏枸杞的单花寿命为(4.07±0.15) d,而雄性持续时间(0.07±0.01 d)比雌性持续时间短(4±0.01 d);花寿命内雌蕊长度比雄蕊长,属柱头探出式异位类型;花粉呈现式样为不完全逐步呈现。(2)花寿命不同阶段花回馈间存在显著差异。(3)意大利蜜蜂(Apis mellifera)、熊蜂(Bombus sp.)、食蚜蝇(Syrphidae sp.)是宁夏枸杞在自然居群的主要访花者,其中熊蜂和食蚜蝇是主要传粉者,但传粉者效率低,属于高移出低沉积类型。(4)宁夏枸杞的花粉胚珠比(2 448.11±448.32)及授粉实验结果均表现出兼性异交特征;自发自交及人工自花授粉花的座果率及结籽率很低,属于自交不亲和类型;自然传粉花的座果率及结籽率比人工去雄异花低,存在其较高的花粉限制(40.71%)。研究发现,宁夏枸杞花部综合征表现出雌雄异位和花粉不完全逐步呈现式样,这是避免雌雄功能及雄蕊各花药间的干扰、减少花粉同步移出及保障其雄性适合度的有效途径,但自然居群的传粉者种类限制、传粉效率低以及自交不亲性是导致宁夏枸杞花粉限制及降低雌性繁殖成功的主要原因。     

塔落岩黄芪主要传粉蜂的传粉效率研究

塔落岩黄芪 (Hedysarum laeve)是毛乌素沙地重要豆科植物, 在我国西部生态系统恢复与重建中起着重要作用, 但其自交率非常低, 必须依靠传粉昆虫授粉才能结实。野生传粉蜂是其主要传粉者。为了明确塔落岩黄芪的主要传粉蜂组成及优势传粉蜂的传粉效率, 2004–2006年, 我们设置了4个2 m×2 m样方观测访花昆虫的组成并对主要传粉蜂的访花频率、花粉移出率和柱头花粉沉降数目及单花停留时间进行了观测。结果表明白脸条蜂(Anthophora albifronella)、海切叶蜂(Megachile maritima)和散熊蜂(Bombus sporsdicus)是塔落岩黄芪的主要传粉蜂, 其中白脸条蜂在数量和访花频率上占有明显优势, 但其花粉移出率比海切叶蜂和散熊蜂的低, 3种蜂的柱头花粉沉降数目没有显著区别。通过对这3种蜂的花粉移出率、柱头花粉沉降数目和访花频率综合分析后, 我们认为白脸条蜂是塔落岩黄芪最有效的传粉蜂。     

橙花瑞香的繁殖特性研究

瑞香属植物具有重要的药用和观赏价值,在中国资源丰富,但自然条件下低坐果率限制了该属植物的进一步开发和利用。该研究以橙花瑞香为对象,通过对其有性繁殖及传粉特性的研究,探索其自然坐果率低的原因,内容包括花部特征的测量分析,MTT染色法测定花粉活性,联苯胺-过氧化氢法测定柱头可授性,扫描电镜观察柱头、花粉的形态,传粉者观察,通过花粉胚珠比(P/O)和人工授粉实验推测橙花瑞香的繁育系统类型。结果表明:橙花瑞香的花部结构特殊,管状小花,花药两轮,雌雄蕊分离。花开后的花粉具有活性,柱头具有可授性,扫描电镜下,柱头和花粉的结构没有发育异常,且柱头上有花粉落置。橙花瑞香的传粉者主要是夜间访花的蛾类,访花频率低。P/O及人工授粉实验表明橙花瑞香的繁育系统为专性异交。橙花瑞香的坐果率非常低,自然坐果率为1.4%,人工异花授粉为23.3%,低坐果率可能是受其开花量大、异花花粉限制、资源限制以及花部结构等因素的影响。     

草乌传粉过程中的广告效应与回报物质研究

虫媒传粉植物与其传粉者之间的相互作用被认为是被子植物花多样性的一个重要选择压力。这种相互作用体现在植物对传粉者的吸引以及传粉者行为对花粉的转运两个方面。本项研究通过去除不同的花部器官研究了草乌(Aconitum kusnezoffii)对其传粉者的吸引, 并结合传粉者的访问行为和草乌花的生物学特性探讨了传粉过程与交配系统的适应。红光熊蜂(Bombus ignites)是草乌的有效传粉者。去除花萼片显著降低了红光熊蜂的访问频率, 但去除特化成蜜腺叶的花瓣并没有显著改变红光熊蜂的访问频率, 这表明草乌吸引红光熊蜂的主要结构是由5枚萼片组成的花部外观形态, 而非花瓣。花蜜是草乌提供给红光熊蜂的回报物质, 糖浓度为39.23%, 组氨酸浓度为0.25 μg/μL。草乌花较大、单花花期长、雌雄异熟、花粉寿命长, 是一个自交亲和但需传粉者传粉完成繁殖过程的异交物种。草乌花序是无限花序, 当上部的花处于雄性阶段时, 下部的花正好处于雌性阶段。而红光熊蜂在草乌花序上的访问顺序通常自下而上, 带来异交花粉为下部的花进行异花授精, 同时又带走上部花的花粉, 这就很好地促进了草乌的异交。草乌雄蕊自外向内逐渐成熟, 是一种有效的限制传粉者单次访问浪费大量花粉的花粉装配策略, 能提高植物通过花粉散布获得的雄性适合度。     

荒漠短命植物异喙菊的小花异形性及繁殖特性

异喙菊(Heteracia szovitsii)是分布于新疆北部荒漠、具短寿命花和多态果实的菊科一年生短命植物。本文对该物种的开花式样和花部特征以及繁育系统与昆虫传粉特性进行了研究,以期明确其头状花序中小花的形态差异及其与多态果实间的关系、揭示其在短的花寿命内的繁殖特性。结果表明:该物种头状花序中发育成多态果实的3类小花在数量、冠毛的有无以及舌片长/宽、子房宽、花柱裂片长和子房喙长之间均存在不同程度的差异,且3类小花冠毛的有无以及子房宽和喙长与多态果实的形态一致,说明多态果实的数量与形态在小花发育过程中就已完成分化。花序中的小花每天集中在上午开放,使花序在功能上犹如一朵花,可快速增大花展示和对传粉者的吸引,以使异交在开花后短时间内完成;3类小花的自花花粉均可在花柱裂片上萌发并长出花粉管,说明该物种自交亲和。3类小花不去雄套袋后均能结实,且自然授粉后的结实率显著高于不去雄套袋的,说明该物种能自主自花授粉,且异花授粉促进了结实。3类小花通过雄性先熟以及次级花粉呈现中的泵/刷机制,将花粉呈现在花柱上部和未展开的柱头裂片外侧刷状毛上以及裂片顶端,延长了花粉呈现(雄性阶段)持续的时间,减少了花内雌雄功能间的干扰,有利于传粉者异花传粉,提高了雄/雌性适合度;同时,柱头裂片展开时可将自花花粉落置到裂片上,以完成自主自花授粉。主要传粉者六显甜花蜂(Halictus sexnotatulus)的访花时间与花序开放时间、花粉活力最高期和柱头最佳授粉期高度吻合,有利于雄性阶段花粉的输出以及雌性阶段柱头接受花粉,保障授粉在开花后短时间内快速有效地完成以及异交成功。在新疆北部荒漠的春季环境中,具短寿命花的异喙菊既可在低温多风导致传粉者不足或活动受限时,通过快速自主自花授粉及自交亲和机制来提供繁殖保障,也可在传粉者活动正常时,通过集中开花、雄性先熟及次级花粉呈现等机制来快速完成异交,提高雌/雄性及后代的适合度。     

琼花生殖器官结构及传粉昆虫的观察

为了探讨影响琼花Viburnum macrocephalum f.keteleeri有性生殖的因素,对其生殖生物学和传粉生物学进行了研究。研究内容主要包括琼花花部特征、生殖器官解剖结构、花粉活力、花粉胚珠比(P/O)、繁育系统、传粉形式、传粉昆虫和花粉管生长路径等。结果表明:(1)琼花聚伞花序由大型不孕花和小型可孕花组成,可孕花雌雄蕊发育正常,雄蕊5枚,雌蕊1枚,干型柱头,单子房,倒生胚珠;不孕花的雌雄蕊在发育早期正常,而在花期时退化。雄蕊退化表现为雄蕊消失、花丝缩短或消失或花药大小不一;而雌蕊退化表现为雌蕊缩小或柱头开裂;有时雌雄蕊也存在瓣化现象。(2)自然条件下,单花花粉活性在散粉4–5d后明显下降,居群花粉活力在4月25日–28日开始显著下降。(3)花粉胚珠比P/O值为12800–18700,属专性异交型;繁育系统为异株异花授粉,属虫媒传粉植物。(4)可孕花大量散粉时间为9:00–16:00,昆虫访花高峰时段为11:00–15:00,访花昆虫中以蝶类和蜂类为主,蝶类访花频率最高。(5)落置柱头的花粉萌发率较高,花粉粒授粉后1h左右开始萌发,花粉管从柱头乳突细胞的间隙穿入花柱,沿花柱中央引导组织生长,18h左右进入子房,20h左右从珠孔进入胚囊。讨论了琼花的不孕花形成、花部结构适应、花型演化趋势、低结实率和花粉管生长特点。     

黑果枸杞两种花型的花部综合征与传粉特性

黑果枸杞(Lycium ruthenicum)是中国西北地区极端环境中分布的国家二级保护植物, 该物种在新疆南部的自然种群中出现了同型花柱类型(同位花)和柱头探出式雌雄异位类型(异位花)个体, 并且遭遇沙尘暴频繁的种群中异位花个体出现频率减少。该研究对喀什市自然种群中黑果枸杞两种不同花型植株的花部综合征和传粉特性进行比较研究, 以期探讨该物种不同花型植株在南疆早春极端环境中的花部特征的可塑性及其适应性机制。结果表明: 同位花雌雄蕊高度间无显著差异, 而异位花雌蕊高度显著高于雄蕊; 同位花花冠直径、花冠筒长、胚珠数均高于异位花, 而异位花雌雄蕊空间距离、花粉数及花粉胚珠比均比同位花高。黑果枸杞同位花个体比例(68%)高于异位花个体(32%), 种群水平及个体水平同位花花期((117.00 ± 2.25) d, (101.65 ± 1.98) d)比异位花((26.00 ± 1.00) d, (18.75 ± 1.00) d)长, 而单花水平上异位花单花寿命((4.50 ± 0.14) d)比同位花((3.13 ± 0.11) d)长。两种类型花在花早期(紫色)分泌的花蜜量均高于花后期(白色)。在紫色花阶段(花开放早期), 同位花上的主要传粉者意大利蜜蜂、熊蜂和食蚜蝇的访花频率和停留时间均高于异位花; 而白色花阶段(花开放后期)意大利蜜蜂、熊蜂在异位花上的访花频率比同位花高。在不同花色阶段, 同位花柱头花粉落置数、花粉移出率、花粉传递效率均比异位花高, 并且同位花自然坐果率及结籽率均比异位花高。在新疆南部的沙尘暴极端环境下, 同位花通过较高的自交亲和性保障繁殖, 而异交为主的异位花提高了异交率。异位花与同位花在花部综合征和花报酬上的差异, 是影响其繁殖成功的主要因素。     

毛菍传粉生物学研究

为探讨毛菍(Melastoma sanguineum Sims.)传粉生物学特性,对海南霸王岭国家级自然保护区林缘、林内和林隙3个生境内毛菍的花期、花部形态、访花昆虫等进行观察,同时对其繁育系统相关指标进行了测定。结果表明：毛菍无花蜜分泌;花瓣对访花昆虫有吸引作用;访花昆虫主要有蜂类、食蚜蝇类和丽金龟类;主要传粉昆虫有木蜂、熊蜂,其中木蜂传粉活动最为活跃,为最有效传粉昆虫。毛菍具典型的异型雄蕊,长、短雄蕊在传粉过程中具有明确的功能分化,推测这是毛菍保证传粉成功的策略。毛菍为自交亲和的异交种,需要昆虫传粉;人工自交和异交均具有较高的坐果率;不存在无融合生殖、主动自花授粉和滞后自交的生殖保障现象;其繁育系统是兼性自交。昼夜温差较小和相对湿度较高的林内和林隙生境有利于延长群体花期;光照充足、温度相对较高的林缘生境,花朵发育较快,柱头可授性的时间稍早。花粉、传粉者和环境条件是制约毛菍野外传粉效率的主要因素。     

重庆特有濒危植物缙云黄芩的繁育系统研究

缙云黄芩（Scutellaria tsinyunensis）为重庆市缙云山特有分布种,目前已经处于濒危状态。本文在定点观测的基础上,运用过氧化氢检测法、花粉-胚珠比（P/O）和套袋实验等方法对缙云黄芩的开花特征和繁育系统进行了分析。结果表明：缙云黄芩花展示和花设计具有适合蜂类等传粉昆虫的传粉综合征,熊蜂(Bombus)和食芽蝇为主要的访花者,P/O为7 618±390,繁育系统为专性异交,传粉套袋实验也证实其必需传粉者异花传粉且可能自交不亲和;其雌雄蕊紧靠的花部结构及花粉活力和柱头可授性低、昆虫的访花频率较低等内外因素致使其自然坐果率较低(20.08%)且结实少(5.6个/株)。由于缙云黄芩小坚果萌发率较低,其有性生殖能力较低,居群扩大困难,应尽快采用人工栽培助其复壮等保护措施。     

贯叶连翘的开花动态与繁育系统研究

野外观察贯叶连翘的开花进程和花部形态特征,运用花粉萌发、杂交指数、花粉-胚珠比等方法测定其繁育系统。结果显示:贯叶连翘雌雄异熟,柱头先花药成熟,雌雄蕊无明显异位。单花花期4～5d。仅在开花当日有昆虫传粉,蜜蜂为主要传粉者。花粉在花药开裂1h后活力最大,萌发率达40.10%,花粉在柱头萌发3h后接近子房。根据杂交指数(OCI)推测其繁育系统属于异交,部分自交亲和,有时需要传粉者。花粉-胚珠比(P/O)则表明贯叶连翘的繁育系统为兼性异交。贯叶连翘结实率低,可能与花粉活力,花粉管的生长速度及花粉在柱头的竞争有关。     

How does secondary pollen presentation affect the fitness of Polygala vayredae (Polygalaceae)?

Secondary pollen presentation is the relocation and presentation of pollen in floral structures (termed pollen presenters) other than the anthers. These pollen presenters are often found close to the stigma and have been hypothesized to increase the accuracy of pollen transfer, although no experimental studies have been done. We examined the function of the pollen presenter and its efficiency in pollen dispersal, female fitness, and the degree of interference created by self-pollen in the shrublet Polygala vayredae, an insect-pollinated species with secondary pollen presentation. Herkogamy, a mechanism generally involved in the reduction of self-interference, was also evaluated. Significant pollen was lost (49% of total pollen) during the secondary relocation in the pollen presenter. However, pollen was exported from the pollen presenter, and subsequent pollen losses were similar to those in species with primary pollen presentation. Despite the presence of a self-incompatibility system, the numbers of developed pollen tubes as well as fruit and seed production were significantly reduced by the self-pollen interference created at the stigmatic papillae level. The extent of herkogamy correlated positively with female fitness. The secondary pollen presentation mechanism may in fact be an accurate system for pollen transport, but it may also have its costs. Further comparative studies involving species with primary and secondary pollen presentation are needed to fully understand the advantages and disadvantages of secondary pollen presentation.     

On the Mechanisms of Secondary Pollen Presentation in the Campanulales-Asterales-Complex1

Families of the Campanulales-Asterales-complex are characterized by special mechanisms for secondary pollen presentation: pump mechanism, brushing mechanism, deposition mechanism, cup mechanism and combination of cup mechanism with brushing mechanism. These different mechanisms are based on three successive events: elongation of the filaments, opening of the anthers, elongation of the style. The diversity of the mechanisms arises through different auxiliary structures such as an indusium, hairs or an anther tube, and the relative rate and time of filament and style growth. An advantage of secondary pollen presentation lies in the prolongation of the male phase of anthesis through portioned pollen release. A probable phylogeny of the different mechanisms of secondary pollen presentation is proposed (Fig. 7).     

Secondary pollen presentation and the temporal dynamics of stylar hair retraction and style elongation in Campanula trachelium (Campanulaceae)

To increase the accuracy of pollen capture and transfer by pollinators some plant species have developed secondary pollen presentation structures. Because the presence of secondary pollen presentation structures at the pistil may reduce the spatial separation between the sexual functions and increase the risk of self‐interference and selfing, temporal segregation of the sexual organs, triggered by visiting insects, can be expected to occur. We investigated secondary pollen presentation and the temporal dynamics of the sexual phases in combination with the physiological self‐incompatibility system in Campanula trachelium, a protandrous insect‐pollinated herb. Stylar hair retraction (male function) and curling of the stigmatic lobes (female function) were modelled using Gompertz growth functions. Finally, we performed pollination experiments in the lab and field to assess seed set and pollen limitation under natural conditions. About 68% of the total pollen load was captured by stylar hairs. Manual manipulation of the stylar hairs, mimicking pollinator visitation, significantly shortened the male phase and accelerated the female phase, resulting in a significant decline in temporal overlap between the two sexual functions. Conversely, when pollinators and/or manual manipulations were lacking, the male phase was substantially prolonged and sexual overlap was maximal. This suggests that spreading of the sexual phases and thus the risk of sexual interference are largely determined by the interaction between stylar hairs and visiting pollinators. Natural seed set was high and not pollinator limited. Overall, these results indicate that secondary pollen presentation and partial protandry resulted in efficient pollen capture, transfer and deposition.     

Anther diversity and function inVerticordia DC. (Myrtaceae)

Anther form and structure across the taxonomic groups inVerticordia were examined. The three anther types which were recognised — rectangular, oblong and saccate, accord well with the three subgenera into which the genus has been divided. The sporogenous part of the anther has a fairly typical angiosperm anatomy. However in many species there is a small or large gland in the upper filament/connective which contains lipidic contents. The anatomy of this structure is based on that of the oil glands which are ubiquitous in Myrtaceae primary tissues. However the gland is usually much larger than these and is schizolysigenous in origin. Evolutionary development of the anthers in the genus is related to pollination systems and the development of secondary pollen presentation from the upper style in some groups. Anther glands may have originally had a protective function for the sporogenous tissue. However in different groups the function has changed or the gland has disappeared. In some species in subgenusChrysoma (which does not have secondary pollen presentation) the gland contents seem to be an additional food source for pollinators. In other groups, with the development of secondary pollen presentation the protective function has become redundant and anther glands have either disappeared or produce contents which have become part of the process of pollen dispersal.     

From anther and pollen ripening to pollen presentation

The events and processes occurring between pollen maturation, opening of the anther and presentation of pollen to dispersing agents are described. In the final phases of pollen development, starch is always stored; this occurs before the anther opens. Depending on the species, this starch may be totally or partially transformed into: (a) other types of polysaccharides (fructans and rarely callose); (b) disaccharides (sucrose); (c) monosaccharides (glucose and fructose, all situated in the cytoplasm. While awaiting dispersing agents and during dispersal, polysaccharides, especially fructans, and sucrose may be interconverted to control osmotic pressure and prevent loss and uptake of water. Opening of the anther is preceded by disappearance of the locular fluid and in many cases by partial dehydration of the pollen. Pollen generally has a water content between 5 and 50%. Pollen with a high water content may or may not be able to control water retention during pollen exposure and dispersal. Pollen may be dispersed in monads or grouped in pollen dispersing units by the following mechanisms: (i). tangling of filamentous pollen; (ii). adhesion by viscous substances (pollenkitt, tryphine, elastoviscin) derived from the tapetum; (iii). common walls. When the anther opens, the pollen may be dispersed immediately, remain until dispersed (primary presentation), or be presented to pollinators in another part of the flower (secondary presentation).     

PROTANDRY,INCOMPATIBILITY, AND SECONDARY POLLEN PRESENTATION IN CEPHALANTHUS OCCIDENTALS (RUBIACEAE)

Cephalanthus occidentalis L. is protandrous and presents pollen secondarily on the stigma surface. Because self-pollen is present on the stigma, the degree of selling vs. outcrossing in this species will depend on 1) the phenology of pollen presentation and stigma receptivity; 2) whether the species is self-incompatible; and 3) the rates of self vs. crossed pollen tube growth. This study describes floral morphology and phenology, self-incompatibility, and pollen tube growth rates in self- and crosspollinations of C. occidentalis. Light and scanning electron microscopy were used to study stigma morphology after flower opening, while controlled pollinations tested for incompatibility. Stigmas were unreceptive initially but became receptive by the second day after flower opening. Ninety-two percent of cross-pollinated flowers set fruit, compared to 12% fruit set in self-pollinations. Pollen tubes from selfed and out-crossed pollen initially had similar growth rates. Out-crossed pollen tubes began to grow rapidly ca. 5 hr after pollination of a receptive stigma, whereas selfed pollen tubes ceased growth or grew slowly after this time. Pollen tubes from out-crossed pollen grew the length of the style within 24 hr after pollination, while selfed pollen tubes were inhibited at the stigma-style junction. Our results indicate that C. occidentalis has selfincompatibility, in addition to protandry and secondary pollen presentation. Protandry allows removal of self-pollen from the unreceptive stigma, while self-incompatibility prevents fertilization by unremoved self-pollen.     

动物传粉植物花粉呈现时序的进化意义

由动物传粉的植物为了使供体花粉能够被高效地传递到受体柱头上, 进化出了多种多样的花部特征, 花粉呈现时序便是其中之一。植物主要通过包装机制和分摊机制控制花粉呈现的速度以限制昆虫一次拜访转移的花粉量。花粉呈现理论(PPT)认为: 花粉逐步呈现策略倾向于出现在传粉者数量丰富但传粉效率低的植物中, 而花粉同时呈现策略则多出现在传粉者少但传粉效率高的植物中。本文对花粉呈现时序的相关研究进行了总结, 重点介绍: (1) 限制花粉转移的花部机制; (2)花粉呈现理论; (3)花粉呈现时序的适应意义。目前的研究主要集中在花粉呈现时序对传粉动物的适应性上, 但环境因子对花粉呈现时序也有一定的影响。PPT数学模型还不能完全预测特定环境中植物的花粉呈现时序。因此, 有必要选择合适的植物类群, 从花部综合特征、传粉系统、交配系统和环境等方面进行综合研究, 进一步揭示动物传粉植物花粉呈现时序的适应意义。     

Pollen grains: Why so many?

My objective is the examination of selective forces that affect pollen number. Relationships among other floral traits of animalpollinated plants, including pollen size, stigma area and depth, and the pollen-bearing area of the pollinator may affect pollen number and also provide a model to examine how change in one trait may elicit change in other traits. The model provides a conceptual framework for appreciating intra- and inter-specific differences in these traits. An equivalent model is presented for wind-pollinated plants. For these plants the distance between putative mates may be the most important factor affecting pollen number. I briefly consider how many pollen grains must reach a stigma to assure fruit set. I use pollen-ovule ratios (P/Os) to examine how breeding system, sexual system, pollen vector, and dispersal unit influence pollen grain number. I also compare the P/Os of plants with primary and secondary pollen presentation and those that provide only pollen as a reward with those that provide nectar as part or all of the reward. There is a substantial decrease in P/O from xenogamy to facultative xenogamy to autogamy. Relative to homoecious species the P/Os of species with most other sexual systems are higher. This suggests that there is a cost associated with changes in sexual system. The P/Os of wind-pollinated plants are substantially higher than those of animal-pollinated plants, and the available data suggest there is little difference in the pollination efficiency of the various animal vectors. The P/Os of plants whose pollen is dispersed in tetrads, polyads, or pollinia are substantially lower than those of species whose pollen is dispersed as monads. There was no difference in the P/Os of plants with primary and secondary pollen presentation. The P/Os of plants that provide only pollen as a reward were higher than those that provide nectar as a reward. All of these conclusions merit additional testing as they are based on samples that are relatively small and/or systematically biased.     

Pollen placement and reproductive isolation between two brazilianPolygala species (Polygalaceae)

Polygala vauthieri andP. monticola var.brizoides have secondary pollen presentation from a basket-like structure on the style apex. This basket is loaded after the first visit by a bee. Pollen reception, therefore, can precede the issue of pollen. A sticky stigma secretion glues the pollen from the basket under the head of the bee visitor in an exactly predetermined spot on the left side only. This position mostly forms a kind of safe spot, where the bee can not remove the pollen. The exact position on the bee's head is determined by the species specific distance between style tip and nectary in the visited flower. In this way the two sympatric species deposit the pollen 2 mm apart on the visitor and so can avoid hybridization pollination, while being visited by the same group of bees.     

Pollenkitt – its composition, forms and functions

Two types of sticky pollen coat material exist in angiosperms, both produced by the anther tapetum. Pollenkitt is the most common adhesive material present around pollen grains of almost all angiosperms pollinated by animals, whereas tryphine seems to be restricted only to Brassicaceae. Tapetal cell protoplasts have different patterns of development according to the products formed during their development and degeneration. If tryphine is formed, the tapetal cell protoplasts lose their individuality at the microspore stage. If pollenkitt is formed, their contents degenerate at later stages. Cell content is totally reabsorbed, when ripe pollen is not surrounded by any gluing material. Current knowledge of pollenkitt formation, deposition on pollen grains and chemical composition are reviewed and discussed. Methods for detecting this viscous fluid are also presented. The many functions of pollenkitt, deduced from personal observations and the literature, act in the period between anther opening and pollen hydration on the stigma; they are: (1) to hold pollen in the anther until dispersal; (2) to enable secondary pollen presentation; (3) to facilitate pollen dispersal; (4) to protect pollen from water loss; (5) to protect pollen from ultra-violet radiation; (6) to maintain sporophytic proteins responsible for pollen–stigma recognition inside exine cavities; (7) to protect pollen protoplasts from fungi and bacteria; (8) to keep together pollen grains during transport; (9) to protect pollen from hydrolysis and exocellular enzymes; (10) to render pollen attractive to animals; (11) to render pollen visible to animal eyes; (12) to hide pollen from animal eyes; (13) to avoid predation of pollen through smell; (14) to enable adhesion to insect bodies; (15) to enable pollen packaging by bees and to form corbicules; (16) to provide a digestible reward for pollinators; (17) to enable pollen clumps to reach the stigma; (18) to allow self-pollination; (19) to facilitate adhesion to the stigma; (20) to facilitate pollen rehydration. Depending on the developmental program of the species, these functions may act during pollen presentation, in relation to pollinators, during pollen dispersal and when pollen reaches the stigma.