荫生鼠尾草的雄蕊变异知多少

为适应昆虫传粉的鼠尾草属植物,在其长期的演化过程中,它们的雄蕊均形成了一种独特的杠杆结构,这已是人们早就知晓的事实。生长在北京郊区小龙门地区的荫生鼠尾草(Salivio umbratica),它与其他鼠尾草属植物一样,在雄蕊结构上与传粉的昆虫之间相互形成了巧妙的适应关系。     

花内雄蕊分化及其适应意义

对花内雄蕊存在显著分化的现象进行了分析与归纳, 总结了花内雄蕊分化的各种主要形式及其繁殖适应意义。“花内雄蕊分化”是指花内雄蕊与雄蕊之间存在显著分化的现象, 这一概念可以把二强雄蕊、四强雄蕊和异型雄蕊等以往单独进行研究的相关性状结合起来, 并明确区分了几种新的花内雄蕊分化形式, 以期更准确全面地认识这些相关性状的适应意义与进化。该文将花内雄蕊分化区别为花丝的分化、花药的分化、雄蕊合生的分化、雄蕊运动的分化、退化雄蕊5大类。花丝的分化主要是花丝长度的分化, 如四强雄蕊、二强雄蕊和单强雄蕊; 花药分化主要指花药颜色、花药与花粉粒大小和花药开裂时间等的分化; 雄蕊合生的分化主要体现为花内部分雄蕊合生而部分雄蕊离生; 雄蕊运动的分化指的是花内雄蕊在运动时间或方式上存在差异, 造成雄蕊处于不同的成熟阶段和位于不同的空间位置; 退化雄蕊则是花内部分雄蕊失去了生产花粉的繁殖功能, 通常也发生了花药形态上的巨大改变。异型雄蕊不仅存在花丝和花药的形态分化, 还存在着明显的功能分化, 是分化程度很高的一类特殊的花内雄蕊分化形式。一些特殊的繁育系统, 如异长花柱和镜像花柱等在种内不同个体上存在着不同形式的花内雄蕊分化。花内雄蕊分化在花内造成了多个不同的花药位置, 在很大程度上影响了雌雄异位程度, 对植物自交与异交水平、花内雌雄功能干扰等有着潜在作用; 花内雄蕊分化形成的多个不同空间位置的雄蕊还增加了对多种访花者的吸引与适应潜力, 有可能影响到访花者的类型与访花行为, 得以适应多种传粉者。此外, 花内雄蕊分化可将花粉逐渐分批次分发给访花者, 提高花粉散布效率, 可看成是“花粉呈现理论”所指的花粉装配与分发机制之一。现有的实验研究发现, 花内雄蕊分化能够吸引传粉者、保护正常花药和花粉、促进花粉散发(降低花粉竞争)、实行延迟自交和降低花内雌雄功能干扰等。花内雄蕊分化还缺少系统研究, 有些雄蕊分化形式如单强雄蕊和雄蕊运动的分化还没有针对性的实验揭示其适应意义, 鸭跖草科和某些豆科植物的雄蕊三型分化等现象也缺少进化适应意义的研究。花内雄蕊分化对植物雌性和雄性适合度可能不同的影响、如何与访花者相互作用、如何与其它花部特征一起影响植物繁殖过程等, 可能是这一领域值得今后优先研究的课题。     

鼠尾草属不同物种的雄蕊杠杆机制对传粉者空间变异的进化响应

被子植物虫媒传粉植物的物种分化通常被认为是花性状响应传粉环境(传粉者)的空间变异而发生适应性分化的结果。通过对鼠尾草属(Salvia) 3个物种(共4个居群)传粉互作系统的比较, 探索了花性状对不同传粉环境的进化响应。结果表明: 各居群的传粉者组成、主要传粉者类型及其大小各不相同, 杠杆状雄蕊及相关花部性状大小在不同居群间具有显著差异; 各居群均表现出腹部传粉和背部传粉2种传粉模式, 但背部传粉仍然是最有效的传粉方式; 居群间杠杆状雄蕊长度与传粉者体长表现出极显著的正相关, 然而花冠长与传粉者体长表现出负相关; 花冠口高度和柱头高度与传粉者胸厚也表现出一定的协同变异。鼠尾草属植物的杠杆状雄蕊及相关花部性状在传粉系统的进化过程中表现出高度的可塑性, 表明雄蕊杠杆传粉机制对传粉环境的变异非常敏感, 在该属植物的物种分化过程中具有关键作用。     

鼠尾草属东亚分支的传粉模式

简述了世界鼠尾草属传粉模式多样性,从宏观层面对东亚鼠尾草属分布中心———中国的鼠尾草属传粉模式进行归纳与总结。研究补充了以往所缺乏的东亚鼠尾草属核心类群的雄蕊结构和传粉模式,并提出雄蕊结构的可能进化方向。根据花器官形态、内部结构、雄蕊特征、花粉接触传粉昆虫的部位,将中国分布的鼠尾草属植物划分为3种模式类型:TypeⅠ,短药隔杠杆传粉模式(short-lever type),主要发生在弧隔鼠尾草亚属(subg.Salvia Benth.),其雄蕊药隔短,属原始结构类型;TypeⅡ,长药隔杠杆传粉模式(long-lever type),主要发生在荔枝草亚属(subg.Sclarea Benth.),雄蕊药隔明显伸长,是典型的背部杠杆传粉结构;TypeⅢ,退化杠杆传粉模式(degraded-lever type),主要发生在鼠尾草亚属(subg.Allagospadonopsis Briq.),花冠筒变短变窄,雄蕊下臂明显退化,传粉者无需进入冠筒即可取食花蜜,花粉触碰昆虫头部,进而杠杆作用弱化。研究表明,鼠尾草属传粉模式的进化趋向于提高传粉者的专一性,同时保证传粉过程的有效性、精确性和忠实性,推测具有退化雄蕊下臂的TypeⅢ模式可能更为进化。比较美洲和地中海2个进化分支的雄蕊结构和进化趋势,东亚多样性中心可能是一个独立的进化分支。毫无疑问,雄蕊结构与花器官和传粉功能高度相关,是适应传粉者的进化表型,它的进化对东亚分支的物种辐射与多样性形成可能具有关键作用。     

光果甘草二体雄蕊的发育及其适应意义

甘草属(Glycyrrhiza)植物具“9 + 1”二体雄蕊, 其中9枚合生雄蕊的上部花丝分离, 分离的花丝在发育过程中存在由早期长、短交错的二组排列方式转变为后期以雄蕊管最长的1枚雄蕊为中心向两边渐次缩短的倒“V”形排列。为了解这种雄蕊发育动态、分化现象及发育成熟后的适应意义, 该文以光果甘草(G. glabra)为实验材料, 比较了雄蕊发育过程中的形态变化、成熟花粉的理化性质及在传粉中的作用。结果显示: 雄蕊发育早期长、短两组雄蕊在花药大小与形状上存在分化, 但后期伴随着花丝的快速生长与花粉的成熟、散出, 花药大小与形状趋于一致; 花粉组织化学成分及授粉成功率无差异, 但成熟花粉的数量和花粉活力存在差异; 去雄处理虽然使访花者在一天内的两个访花高峰期的访花频次降低, 但结实率高于自然对照, 说明以异交为主的花去除雄蕊后, 降低了雌、雄蕊间的功能干扰, 提高了传粉昆虫的授粉率; 发育早期长、短交错排列的二组雄蕊到成熟期时发生的倒“V”形排列的转变, 使不同数量与活性的花粉分布在花内不同空间, 最大化接触访花者, 实现了资源节约, 提高了雄蕊的雄性适合度, 即在有限的空间内用最节约的雄性资源投入、使传粉空间与传粉几率最大化的方式, 来提高雄性功能。     

舌瓣鼠尾草退化杠杆雄蕊的相关花部特征及传粉机制

杠杆状雄蕊是鼠尾草属(Salvia)物种形成的关键性状, 背部杠杆传粉模式作为该属植物与传粉者精确互作的经典案例被广泛深入研究, 但是在该属物种中还存在许多非典型的杠杆结构和传粉模式。雄蕊结构及其与传粉者互作的多样性, 使得鼠尾草属成为研究植物传粉模式转变的模式材料, 舌瓣鼠尾草(S. liguliloba)即是一种具非典型的退化杠杆状雄蕊结构和传粉特征的代表性物种。该文着重对舌瓣鼠尾草的花器官结构和传粉特征进行研究, 并与具有短药隔杠杆的毛地黄鼠尾草 (S. digitaloides)做比较分析, 以期揭示退化杠杆可能的进化选择压力及其生态学意义。结果表明, 舌瓣鼠尾草具有较短的花冠、更窄的冠筒和较短的雄、雌蕊(p < 0.05)。退化萎缩的雄蕊下臂, 冠筒内的狭小空间限制了唯一的有效传粉昆虫——三条熊蜂(Bombus trifasciatus)推动雄蕊做杠杆状运动, 而是靠近花药直接利用头部完成授粉。相比经典的杠杆状雄蕊结构及其传粉过程, 小型花冠和退化杠杆雄蕊是对专一性和活跃度较高传粉昆虫的适应, 可能具有完全不同的进化途径和繁殖策略。     

植物雄蕊合生的多样性、适应意义及分类学意义初探

定义并总结了雄蕊合生现象,对雄蕊合生的类型、适应意义、进化及分类学意义进行了初步的讨论和总结.本文定义"雄蕊合生"为,花内雄蕊与雄蕊之间部分或整体的结合生长,既包括愈合与黏合,也包括结合紧密的贴生和靠生.根据雄蕊合生部位的不同,将雄蕊合牛分为"花丝合生"、"花药合生"和"花丝花药均合生"等三大类.每一类中还存在着合生程度不同的子类型.雄蕊合生的结构还可能进一步与柱头或花柱合生在一起,形成"合蕊柱"一类的复杂结构.雄蕊合生在裸子植物较进化的科如百岁兰科和买麻藤科中就出现了,在种子植物中集中分布在近50个科内,且从系统关系来看,雄蕊合生各个类型可能发生过多次进化上的反复.在被子植物中,花丝合生类型更多地与较早进化的类群联系在一起,且多出现在离瓣花中;花药合生及花丝花药均合生则较晚进化,多与有着明显花冠筒的合瓣花伴随出现.这暗示着,雄蕊的合牛结构有可能与花部其他特征一起影响了植物的繁殖过程,具有一定的适应意义.目前,还没有实验研究针对雄蕊合生各个类型开展实验以揭示其发育机制和适应意义.理论上,花丝合乍能增强雄蕊的强度,有时候还形成了围绕子房与花柱的杯状、管状或环状结构,能对子房和花柱有着保护作用且承受传粉者在花内移动的压力:花丝合生还可将雄蕊固定在一个较为稳定的位置,使得花药接触传粉者身体的部位相对固定,减少了花粉浪费.花药合生能将花内花药都集中到同一个位置,花粉接触传粉者身体的同一部位,从而降低花粉损耗和提高异交授粉的准确性.花丝花药均合生可以同时具有以上两种合生方式的适应意义,而且还极大改变了雄蕊的结构与空间位置,改变了花药与柱头之间的空间位置(雌雄异位),对花内自交可能性和雌雄功能干扰有着潜在的影响.雄蕊合生各个类型的适应意义及其对访花者类型与行为和植物繁殖策略的影响,还需要开展实验进行针对性的研究.由于雄蕊形态与结构较为稳定,雄蕊合生的不同方式以及合生程度可以作为科与种的分类参考.     

植物居群的基因流动态及其相关适应进化的研究进展

生物自然居群间的基因流不但可以阻止遗传分化以维持物种的完整性, 而且也能积极响应生物多样化的进程。理解与基因流相关的适应性进化及其内在机理将有助于我们更好地认识生物物种形成和多样化的原始动力以及真正原因。该文通过对植物种内和种间居群基因流动态进行讨论, 阐述了近年来有关植物基因流动态的一些重要理论观念和研究进展, 以期为相关领域动态及趋势研究提供参考。     

植物居群的基因流动态及其相关适应进化的研究进展

生物自然居群间的基因流不但可以阻止遗传分化以维持物种的完整性,而且也能积极响应生物多样化的进程。理解与基因流相关的适应性进化及其内在机理将有助于我们更好地认识生物物种形成和多样化的原始动力以及真正原因。该文通过对植物种内和种间居群基因流动态进行讨论,阐述了近年来有关植物基因流动态的一些重要理论观念和研究进展,以期为相关领域动态及趋势研究提供参考。     

两性花的雄蕊运动:多样性和适应意义

雄蕊运动指雄蕊在自身能量支持下发生的主动运动,不包括雄蕊在访花者触碰下造成的被动位移。该文总结了雄蕊的应激运动、快速猛烈弹射、缓慢运动以及级联运动等4种主要类型,分析了这些运动类型的系统分布及繁殖适应意义等方面的研究进展。雄蕊的应激运动由访花者或其他外力诱发,可能起到促进散粉和实现繁殖保障的作用;雄蕊快速猛烈的弹射运动可将花粉猛然撒向空中或访花者身上,促进了花粉的风媒或虫媒散布;缓慢运动的雄蕊可能通过在不同花期改变雄蕊的空间位置和雌雄异位程度来调节繁殖策略,或主动将雄蕊花药移至特定部位(如柱头表面)实现自交;雄蕊逐一、依次发生的级联运动较为复杂,主要分布在刺莲花科、梅花草科、旱金莲科和芸香科中,目前还缺乏实验研究;但根据\"花粉呈现理论\"以及其他类型的雄蕊运动研究结果,雄蕊的级联运动可以将花粉分批呈现给不同的传粉者,通过不同传粉者的分别传粉来提高花粉的输出;而且可避免已散粉雄蕊对即将散粉雄蕊的干扰,同时可能也降低了雌雄功能干扰和(或)花内自交。在芸香(Ruta graveolens)中,级联运动之后的雄蕊还会在花末期再同时向花中央运动;这种多向、多次运动方式是目前发现的最复杂的雄蕊运动类型。雄蕊运动领域值得今后开展进一步实验研究的方向主要有:1)雄蕊运动尤其是级联运动对雌雄功能干扰(性别间干扰)、雄蕊与雄蕊的\"性别内干扰\"等植物繁殖格局的影响;2)雄蕊运动与雌雄异熟、雌雄异位等花部特征的相互作用;3)雄蕊运动复杂类型的生理与发育机制。     

The pollination niche and its role in the diversification and maintenance of the southern African flora

The flora of southern Africa has exceptional species richness and endemism, making it an ideal system for studying the patterns and processes of evolutionary diversification. Using a wealth of recent case studies, I examine the evidence for pollinator-driven diversification in this flora. Pollination systems, which represent available niches for ecological diversification, are characterized in southern Africa by a high level of ecological and evolutionary specialization on the part of plants, and, in some cases, by pollinators as well. These systems are asymmetric, with entire plant guilds commonly specialized for a particular pollinator species or functional type, resulting in obvious convergent floral evolution among guild members. Identified modes of plant lineage diversification involving adaptation to pollinators in these guilds include (i) shifts between pollination systems, (ii) divergent use of the same pollinator, (iii) coevolution, (iv) trait tracking, and (v) floral mimicry of different model species. Microevolutionary studies confirm that pollinator shifts can be precipitated when a plant species encounters a novel pollinator fauna on its range margin, and macroevolutionary studies confirm frequent pollinator shifts associated with lineage diversification. As Darwin first noted, evolutionary specialization for particular pollinators, when resulting in ecological dependency, may increase the risk of plant extinction. I thus also consider the evidence that disturbance provokes pollination failure in some southern African plants with specialized pollination systems.     

Systematics and evolution of the Disa draconis complex (Orchidaceae)

The systematic status of Disa draconis (L.f.) Sw. is revised following extensive field studies of population variation in the Western Cape, South Africa. Principal component and cluster analyses revealed clear distinctions between populations from sandplain, semi-arid and montane environments. Diagnostic characters were found in each of the population clusters indicating the existence of a species complex, rather than a single taxon as in the current taxonomy. We propose, therefore, that the name D. draconis (L.f.) Sw. be restricted to the individuals of the sandplain populations from which the type was collected. We reinstate an earlier name, Disa harveiana Lindl., to describe the montane populations which possess several autapomorphic characters. We also show that the geographical variation in spur length and flowering time within this species can be partitioned into two geographically distinct subspecies: D. harveiana subsp. harveiana and D. harveiana subsp. longicalcarata Johnson & Linder. The populations from the semi-arid Karoo region were recognized as a distinct new species, Disa karooica Johnson & Linder, on the basis of their peculiar petal structure. A cladistic analysis indicated that the three species forming the D. draconis complex form a monophyletic and relatively specialized lineage within Disa sect. Coryphaea. The revised classification also has important conservation implications as D. draconis , previously considered a common species, is now restricted to a few highly threatened populations on the west coast near Cape Town.     

Resource polyphenism increases species richness: a test of the hypothesis

A major goal of evolutionary biology is to identify the causes of diversification and to ascertain why some evolutionary lineages are especially diverse. Evolutionary biologists have long speculated that polyphenism—where a single genome produces alternative phenotypes in response to different environmental stimuli—facilitates speciation, especially when these alternative phenotypes differ in resource or habitat use, i.e. resource polyphenism. Here, we present a series of replicated sister-group comparisons showing that fishes and amphibian clades in which resource polyphenism has evolved are more species rich, and have broader geographical ranges, than closely related clades lacking resource polyphenism. Resource polyphenism may promote diversification by facilitating each of the different stages of the speciation process (isolation, divergence, reproductive isolation) and/or by reducing a lineage''s risk of extinction. Generally, resource polyphenism may play a key role in fostering diversity, and species in which resource polyphenism has evolved may be predisposed to diversify.     

A preliminary classification of evolutionary radiations

Rapid increases in taxonomic diversity are generally described as adaptive or evolutionary radiations. Such radiations differ widely in the rate and extent of morphologic innovation, taxonomic diversification and phylogenetic breadth, suggesting that several patterns, and likely processes, are involved. At least four distinct patterns of evolutionary radiation can be identified: novelty events, which generate new morphological complexity (altering the body plan of the group under consideration) but not necessarily with the associated production of many lower taxa; broad diversification events involving many independent lineages that undergo diversification, generate many new species and are driven by new ecological opportunities; economic radiations of a limited group of ecologically (but not necessarily phylogenetically) related clades exploiting a limited new ecologic opportunity; and adaptive radiations that may occur at any taxonomic level, but involve a rapid increase in diversity within a single clade, including “true”; adaptive radiations. Many events produce simple diversity increases with no corresponding increase in genetic/developmental/morphological/behavioral sophistication, but the most evolutionarily interesting events add new levels of complexity.     

Phylogeny and radiation of pollination systems in DISA (Orchidaceae)

We studied the patterns of adaptive radiation in Disa, a large orchid genus in southern Africa. A cladogram for 27 species was constructed using 44 morphological characters. Pollination systems were then mapped onto the phylogeny in order to analyze pathways of floral evolution. Shifts from one pollination system to another have been a major feature of the evolutionary diversification of Disa. Unlike many plant genera that are pollinated mainly by a single group of insects, radiation in Disa has encompassed nearly all major groups of pollinating insects; in all, 19 different specialized pollination systems have been found in the 27 species included in this analysis. Another striking pattern is the repeated evolution of broadly similar pollination systems in unrelated clades. For example, butterfly-pollinated flowers have evolved twice; showy deceptive flowers pollinated by carpenter bees, twice; long-spurred flowers pollinated by long-tongued flies, four times; night-scented flowers pollinated by moths, three times; and self-pollination, three times. This suggests that a few dominant pollinator species in a region may be sufficient to generate diversification in plants through repeated floral shifts that never retrace the same pathways.     

Remarkable new evidence for island radiation in birds

If island biogeography has a sweet spot, it's where islands generate their own species diversity rather than merely taking on mainland immigrants. In birds and other highly dispersive taxa, however, this 'zone of radiation', may be vanishingly small. Darwin's finches and Hawaiian Honeycreepers are among only a handful of examples of island radiation in birds (Price 2008), suggesting that winged powers of dispersal make sufficient isolation from mainland colonists unlikely, while also hindering speciation within and among isolated islands. Nevertheless, two studies in this issue of Molecular Ecology join a string of other recent analyses suggesting that island radiation in birds remains under-appreciated (see also Moyle et al. 2009; Kisel & Barraclough 2010; Rosindell & Phillimore 2011). Melo et al. (2011) use a phylogenetic analysis of white-eyes on islands in the Gulf of Guinea to identify two previously overlooked island radiations, and reveal replicated adaptive divergence on islands where species occur in pairs. Sly et al. (2011), meanwhile, consider possible explanations for speciation and geographic differentiation within a large island, and find the same type of oceanic barriers that are critical to bird speciation across archipelagos may also contribute to divergence that appears to have occurred within a single island.