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1.
 多年来, 不同繁育系统的榕树(Ficus spp.)的进化问题引起生物学家们极大的兴趣。前人通过对不同繁育系统榕树雌花的花柱长度、传粉榕小蜂产卵器长度和繁殖率的比较, 推测榕树的雌雄异株是由雌雄同株进化而来的。为验证这一推论, 选取雌雄同株的垂叶榕(Ficus benjamina)和钝叶榕(F. curtipes)以及雌雄异株的斜叶榕(F. tinctoria)和鸡嗉子榕(F. semicordata), 进行了雌花花柱长度、传粉榕小蜂产卵器长度及繁殖率的比较。研究结果显示: 1)两种雌雄同株榕树的传粉榕小蜂(Eupristina koningsbergeri和Eupristina sp.)的产卵器长度, 显著长于两种雌雄异株榕树的传粉榕小蜂(Liporrhopalum gibbosae和Ceratosolen gravelyi)产卵器的长度, 且雌雄同株榕树雌花花柱长度的变异大于雌雄异株雌花花柱长度的变异; 2)两种雌雄同株榕树的雌花花柱长度呈单峰分布, 且花柱长度的变异大于传粉榕小蜂产卵器长度的变异; 两种雌雄异株榕树花序的雌花花柱长度呈双峰分布, 雌花花柱长度的变异也大于传粉榕小蜂产卵器的长度变异; 3)两种雌雄同株榕树的传粉榕小蜂产卵器长度能到达雌花子房的比例更高, 可更有效地产生瘿花, 而雌雄异株榕树产生种子的优势更强。研究表明: 在传粉榕小蜂产卵器长度及花序雌花花柱分布方面, 雌雄异株榕树有着明显的优势, 但在繁殖率方面没有绝对优势。因此, 前人从雌花花柱分布及繁殖率比较而做出榕树进化的推测并不正确。要真正解决榕树的进化问题, 需要多学科、多指标的综合分析和深入研究。  相似文献   

2.
张媛  杨大荣  彭艳琼 《植物生态学报》2010,34(11):1303-1309
榕树(Ficusspp.)及其传粉榕小蜂(Agaonidae)之间经过长期的协同进化,已形成了高度专一的互惠共生关系。在雌雄同株的榕树中,同一个榕果内既繁殖种子,又繁殖榕小蜂,雌花资源在繁殖种子和榕小蜂之间是怎样分配的?该研究选择广泛分布于西双版纳地区的高榕(F.altissima)及其传粉榕小蜂系统来回答这个问题。高榕果内的雌花柱头形态变异较大,有3种类型的柱头——球型、弯钩型和火炬型,它们分别占到雌花总量的54.00%、36.93%和9.07%。3种类型柱头的雌花分别具有不同长度的花柱,球型柱头雌花的平均花柱长度最短,火炬型柱头次之,弯钩型柱头雌花的平均花柱长度最长。在高榕果内,有传粉者Eupristina altissima和欺骗者Eupristina sp.两类小蜂进入榕果内繁殖,前者的产卵器长度比96.01%以上的雌花花柱长,后者的产卵器也要长于85.73%的雌花花柱,从产卵器长度和雌花花柱长度的匹配情况看,它们应该可以利用绝大多数雌花产卵繁殖后代。然而,繁殖榕小蜂的雌花主要是短花柱的雌花,其中60.64%是球型柱头的雌花;而繁殖种子的主要是花柱较长的弯钩型柱头和火炬型柱头的雌花。显然,繁殖榕小蜂和种子的雌花不仅花柱长度有差异,柱头也分化出了不同的形态,变异的柱头形状也是调节榕树-榕小蜂繁殖平衡的手段之一。  相似文献   

3.
榕树与其传粉榕小蜂的共生关系常被认为是专一性的,但该系统中有些榕小蜂可在不同种榕树或者同种榕树的不同亚种、变种和地理型上产卵和传粉。探讨榕小蜂在不同寄主中的繁殖和传粉特征,有利于理解非专性榕蜂系统形成的过程及稳定机制。本研究中,作者分别对比分析了传粉榕小蜂Ceratosolen emarginatus在木瓜榕(Ficus auriculata)的两种地理型auriculata-form和oligodon-form上的产卵和传粉特征。结果显示,进蜂量为1,2,3只时,相同寄主上的榕小蜂后代和种子数量均随进蜂量的增加而增加,且平均单只繁殖雌蜂的后代及种子数量均无差异。这可能是由于进蜂量较低时,两寄主可被利用的繁殖资源较充足,榕小蜂间不存在干扰竞争,可最大化地利用雌花资源。另一方面,进蜂量相同时,同一寄主上产生的种子数量明显多于榕小蜂后代数量,说明榕树的繁殖利益更占优势。榕小蜂在auriculata-form上产生的后代总量和平均单只雌蜂后代数量与oligodon-form均无差异,但后者产生的种子数量明显多于前者,说明当繁殖资源充足时寄主不影响榕小蜂的繁殖,然而寄主差异影响种子产生,即auriculata-form和oligodon-form的繁殖能力已发生分化。  相似文献   

4.
榕属植物及其传粉昆虫榕小蜂是自然界协同进化的经典模型,榕果内雌花资源如何分配一直是备受关注的问题。为验证季节变化对榕树-榕小蜂互利共生系统生长与繁殖的影响,该研究以西双版纳地区的聚果榕(Ficus racemosa)为材料,分析了季节变化对榕果大小、自然进蜂量以及榕树-榕小蜂繁殖的影响,并利用人工控制性放蜂实验和模型拟合,探讨榕果最适进蜂量及不同季节进蜂量对雌花资源分配的影响。结果表明:季节对榕果直径有显著影响,雨季的榕果直径显著小于干热季和雾凉季;不同季节的自然进蜂量也有显著差别,苞片口对调节进蜂数量有重要作用;季节对榕树-榕小蜂繁殖分配也有影响,雾凉季产生的种子数量和榕小蜂数量均最多;同时人工控制实验和二次抛物线模型拟合结果表明,母代雌蜂数量与种子及榕小蜂后代数量均呈抛物线关系,雌蜂数量过多或过少都对榕树-榕小蜂的繁殖不利,自然进蜂量与拟合的最优进蜂量基本一致。研究结果说明榕果进化出了适应西双版纳地区季节变化的繁殖策略。  相似文献   

5.
 榕树(Ficus)及其传粉榕小蜂(Agaonidae)构成了高度专一的互惠共生体系。榕树的果实(以下简称榕果)内也寄生着一些非传粉小蜂。 绝大多数非传粉小蜂在榕果外把产卵器刺入果壁产卵到果腔内, 只有极少数种类能够进入果腔内产卵。在西双版纳地区, 钝叶榕(Ficus curtipes)上的杨氏榕树金小蜂(Diaziella yangi)类似于传粉者钝叶榕小蜂(Eupristina sp.), 它也是进入榕果内产卵繁殖后代的, 这就为比 较研究榕果内产卵小蜂与寄主榕树间的关系提供了材料。该文从形态学、行为学和生态学角度比较研究了这两种进入榕果内产卵的小蜂与寄主 钝叶榕之间的作用关系, 研究结果显示: 1)杨氏榕树金小蜂与钝叶榕小蜂的雌蜂头部形状存在趋同进化; 2)两种小蜂的产卵器的平均长度都比 雌花花柱长, 因而能把卵产在子房里; 3)钝叶榕小蜂从瘿花出来需要3~5 h, 交配需要17~19 min, 杨氏榕树金小蜂从瘿花出来只需18~20 min, 交配时间为20~30 s; 4)在自然群落中, 大约90%的雌花期榕果里都只进一只杨氏榕树金小蜂和一只钝叶榕小蜂, 杨氏榕树金小蜂能通过传粉来 增加榕树种子数量, 但对钝叶榕小蜂种群的繁衍造成了极显著的负面影响; 5)两种小蜂于同一时期进入榕果内繁殖, 子代同期成熟羽化, 发育 期与榕树雄花的发育期同步。研究表明: 进入榕果内繁殖的两种小蜂与寄主榕树之间存在着协同进化关系, 杨氏榕树金小蜂为榕树有效地传粉, 这可能是一个由寄生者向互惠方向进化的实例。  相似文献   

6.
张凤萍  彭艳琼  杨大荣 《生态学报》2009,29(10):5252-5257
钝叶榕 (Ficus curtipes)是雌雄同株,它除了依赖钝叶榕传粉榕小蜂Eupristina sp.传粉外,另外两种进入果内繁殖的杨氏榕树金小蜂Diaziella yangi 和Lipothymus sp.金小蜂也能有效地为它传粉,这3种小蜂同时产卵于雌花的子房内,在榕果内繁殖后代.通过控制性放蜂试验,比较研究钝叶榕3种传粉者的传粉效率,结果表明:自然状态下,3种小蜂在绝大多数榕果里只各进1头.在控制性放蜂试验中,3种小蜂的传粉效率均随着放入雌蜂数量的增加而增加,两种金小蜂的传粉效率有时比钝叶榕传粉榕小蜂的传粉效率还高.当钝叶榕传粉榕小蜂分别与两种金小蜂同时放入榕果内传粉时,其生产的种子数量居于或者是接近两种小蜂单独传粉时形成的种子数量,传粉效率没有显著增加.在比较3种小蜂单种分别放1头和2头的传粉效率时,增加单果放蜂数量,钝叶榕传粉榕小蜂和Lipothymus sp. 的平均传粉效率降低,但杨氏榕树金小蜂的平均传粉效率是增加的.对3种不同属传粉小蜂传粉效率的比较,可为研究榕-蜂互惠系统的互惠的起源提供依据.  相似文献   

7.
【目的】榕树(Ficus)依赖专性榕小蜂(Agaonidae)传粉,同时为传粉榕小蜂提供繁衍后代的场所,两者形成动植物间经典的协同进化关系。在雌花期果内,榕小蜂需在有限的存活时间内完成传粉和产卵,而传粉榕小蜂如何在传粉与产卵之间进行权衡仍然是悬而未解的问题。本研究旨在明确传粉榕小蜂——一种栉颚榕小蜂Ceratosolen sp.在雌雄同株的聚果榕Ficus racemosa雌花期果内的行为活动及繁殖模式。【方法】借助测微尺测量聚果榕榕果雌花花柱长度与传粉榕小蜂(Ceratosolen sp.)产卵器长度,通过显微视频记录传粉榕小蜂在雌花期果内搜索、传粉及产卵行为;结合单果控制性引蜂试验,测定不同阶段榕小蜂个体大小、孕卵量、携粉量,以及雄花期最终繁殖的榕小蜂后代和榕果种子数量。【结果】聚果榕雌花花柱长度存在树间变异,榕小蜂产卵器长度比绝大多数的雌花花柱长,说明该小蜂可以产卵于大部分的雌花子房里。通常个体大的榕小蜂孕卵量更多,但个体大小与携粉量之间相关性不显著。观察发现,榕小蜂进入雌花期榕果内,前6 h集中产卵,可产下孕卵量的95%,平均搜索用时27 s,产卵用时46 s,此期间传粉行为少见,花粉筐中携带花粉量亦无明显变化;榕小蜂进果后6-24 h,主要执行传粉,其行为主动,连贯高效,单次传粉用时平均为2 s,最终可传完携粉量的80%。控制引蜂试验也证实榕小蜂进入榕果内前6 h主要执行产卵繁殖后代,之后6-24 h主要执行传粉以繁殖榕树种子。【结论】在雌雄同株的聚果榕雌花期榕果内,榕小蜂先产卵、后传粉。本研究首次展示了传粉榕小蜂在聚果榕雌花期榕果内的产卵和传粉行为,并获得与行为相匹配的产卵量和传粉繁殖量,反映了具主动传粉行为的榕小蜂在传粉和产卵之间存在时间和数量上的权衡。  相似文献   

8.
西双版纳热带雨林对叶榕传粉生物学(英)   总被引:9,自引:0,他引:9  
研究了西双版纳热带雨林地区雌雄异株植物对叶榕 (FicushispidaL .)的生物学、传粉物候学以及榕小蜂(CeratosolensolmsimarchaliMayr)的传粉和繁殖行为。研究结果表明 :雌雄异株的对叶榕与其他雌雄同株的榕属植物不同 ,它的种子形成与传粉者有着更为复杂的相互关系。对叶榕一年结隐花果 6~ 8次 ,结果高峰期 4~ 5次 ,其中雄性植株仅产生花粉和孕育榕小蜂 ,而雌性植株 (无雄蕊 )则需榕小蜂带花粉进入隐花果内 ,进行传粉授精 ,使之发育成种子。对叶榕的成熟花粉不能从花药开裂处自行散发出来 ,必须由榕小蜂采集才能散落。榕小蜂雌蜂羽化、交配后 ,找到雄花区 ,用足、触角、口器在推动中采集花粉。雌蜂飞出熟榕果找寻雌株或雄株榕树上的幼嫩隐花果 ,一般需 3~ 6 7min ;一部分雌蜂在雄株中寻找幼嫩的隐花果 ,进去产卵繁殖 ,另一部分雌蜂则寻找雌株雌花期嫩隐花果进去传粉。雌蜂在雌株榕树的隐花果内传粉时间为 15~ 2 3h ,在雄株榕树的隐花果内产卵时间为 6~ 9h。对叶榕小蜂在雌株上进入单个隐花果的数量多少关系到雌花结实率 ;观察表明 ,每个隐花果最佳进蜂数为 2头 ;榕小蜂传粉后榕树成熟种子形成率在 5 4 .1%~ 82 .5 %之间 ,平均为 73.8% ;而在雄株上雌蜂进蜂数量则关系到榕小蜂在隐花果内的产卵率 ,  相似文献   

9.
【目的】榕树(Ficus)依赖专性榕小蜂(Agaonidae)传粉,同时为传粉榕小蜂提供繁衍后代的场所,两者形成动植物间经典的协同进化关系。在雌花期果内,榕小蜂需在有限的存活时间内完成传粉和产卵,而传粉榕小蜂如何在传粉与产卵之间进行权衡仍然是悬而未解的问题。本研究旨在明确传粉榕小蜂——一种栉颚榕小蜂Ceratosolen sp.在雌雄同株的聚果榕Ficus racemosa雌花期果内的行为活动及繁殖模式。【方法】借助测微尺测量聚果榕榕果雌花花柱长度与传粉榕小蜂(Ceratosolen sp.)产卵器长度,通过显微视频记录传粉榕小蜂在雌花期果内搜索、传粉及产卵行为;结合单果控制性引蜂试验,测定不同阶段榕小蜂个体大小、孕卵量、携粉量,以及雄花期最终繁殖的榕小蜂后代和榕果种子数量。【结果】聚果榕雌花花柱长度存在树间变异,榕小蜂产卵器长度比绝大多数的雌花花柱长,说明该小蜂可以产卵于大部分的雌花子房里。通常个体大的榕小蜂孕卵量更多,但个体大小与携粉量之间相关性不显著。观察发现,榕小蜂进入雌花期榕果内,前6 h集中产卵,可产下孕卵量的95%,平均搜索用时27 s,产卵用时46 s,此期间传粉行为少见,花粉筐中携带花粉量亦无明显变化;榕小蜂进果后6-24 h,主要执行传粉,其行为主动,连贯高效,单次传粉用时平均为2 s,最终可传完携粉量的80%。控制引蜂试验也证实榕小蜂进入榕果内前6 h主要执行产卵繁殖后代,之后6-24 h主要执行传粉以繁殖榕树种子。【结论】在雌雄同株的聚果榕雌花期榕果内,榕小蜂先产卵、后传粉。本研究首次展示了传粉榕小蜂在聚果榕雌花期榕果内的产卵和传粉行为,并获得与行为相匹配的产卵量和传粉繁殖量,反映了具主动传粉行为的榕小蜂在传粉和产卵之间存在时间和数量上的权衡。  相似文献   

10.
传粉榕小蜂与榕树的繁衍   总被引:10,自引:2,他引:8       下载免费PDF全文
榕树传粉现象被广泛地作为研究协同进化特别是互惠共生的重要模式之一。本文总结了榕果与传粉榕小蜂的有关研究,试图解释其形态结构之间的相互适应,总结传粉榕小蜂的传粉行为,探讨传粉榕小蜂在雌雄同株及雌雄异株榕树上的传粉模式,讨论传粉榕小蜂的寄主专一性,并展望中国在榕小蜂方面的研究前景。  相似文献   

11.
Fig trees (Ficus: Moraceae) are pollinated by female fig wasps (Agaonidae) whose larvae develop inside galled flowers of unusual inflorescences (figs). Most fig trees also support communities of non‐pollinating fig wasps. Figs of different species display great size variation and contain tens to tens of thousands of flowers. Around one‐half the species of fig trees have the gynodioecious breeding system, where female trees have figs that produce seeds and male trees have figs that support development of pollinators. Mutual mimicry between receptive male and female figs ensures that pollinators enter female figs, even though the insects will die without reproducing, but the need to give no sex‐specific cues to the pollinators may constrain differences in size between receptive male and female figs. We compared relationships between inflorescence size and some measures of reproductive success in male and female figs of Ficus montana grown under controlled conditions in the presence of the pollinator Kradibia tentacularis and its main parasitoid Sycoscapter sp. indesc. Female figs that contained more flowers produced more seeds, but male figs did not increase the production of female pollinator K. tentacularis fig wasps in proportion of the flower number. Although more flowers were galled by the pollinators in male figs containing more female flowers, the high larval mortality caused by parasitism and nutritional limitation prevented the increase in the production of adult female offspring. Selection may favor the increase in flower numbers within figs in female plants of F. montana, but contrarily constrain this attribute in male plants.  相似文献   

12.
Abstract. Plants pollinated by specialists are often thought to receive exceptionally high-quality pollinator service, but in relatively low and unpredictable quantities. We examine and reject this hypothesis for an obligate mutualism between a subtropical New World fig ( Ficus aurea ) and its species-specific pollinator ( Pegoscapus jimenezi ). Fig wasps lay eggs within the flowers they pollinate; their offspring destroy a large proportion of fig's seeds. In a 6-year study of this interaction in Florida, U.S.A., we found that pollination intensity was in fact relatively high. Also contrary to expectations, reproductive success of both mutualists (as well as other wasps cohabiting the figs) was extremely variable and generally low, at three different scales of sampling: among figs from a single crop of one tree (thirty-four figs), among crops produced at different times by that tree (126 figs), and across trees over a 1-year period (379 figs). Although variable, fig contents were not completely unpredictable. For example, seed and wasp numbers increased with the number of flowers in a fig, and female and male flower numbers increased together. Little is yet known about the causes either of these relationships or of the massive fig-to-fig variation itself, although there is some evidence that they exist in other fig species as well. Further investigations of these patterns should shed new light on the ecology and evolution of this mutualism.  相似文献   

13.
The nursery pollination system of fig trees (Ficus) results in the plants providing resources for pollinator fig wasp larvae as part of their male reproductive investment, with selection determining relative investment into pollinating wasps and the pollen they carry. The small size of Ficus pollen suggests that the quantities of pollen transported by individual wasps often limits male reproductive success. We assessed variation in fig wasp pollen loads and its influence on seed production in actively pollinated (Ficus montana) and passively pollinated (Ficus carica) dioecious fig trees.The ratios of number of male flowers on number of female flowers in a glasshouse-maintained F. montana population were highly variable. When fig wasps were introduced into receptive female figs, the resulting seed numbers were strongly linked to the numbers of pollinators that had been seeking access to pollen, relative to the number of anthers in their natal figs. In F. carica estimates of the amounts of pollen produced per fig and the quantities of pollen carried by emerging fig wasps suggest that less than 10% of the pollen is transported. Pollinators of F. carica that emerged earlier from figs carried more pollen, and also generated more seeds when introduced into receptive female figs.We show here that all pollinators are not equally valuable and producing more pollinators is not necessarily a good option in terms of Ficus male fitness. Previous results on F. montana figs showed that only around half of the flowers where pollinators lay eggs produced adult offspring. The amount of pollen collected by young female fig wasps may be a major determinant of their reproductive success.  相似文献   

14.
15.
Figs and their pollinating fig wasps are dependent on one another for propagation of their own kinds. The wasps reproduce by ovipositing through the styles of female flowers within the closed fig receptacles (syconia). About half of the female flowers within the syconia of monoecious figs have styles which are longer than the ovipositors of the wasp, and they will therefore produce seeds rather than wasp larvae. Since a longer ovipositor would enable a wasp to reach more ovules and deposit more eggs, the question arises at to why longer ovipositors have not evolved.
In an attempt to answer this question, four seemingly plausible hypotheses are examined but each is shown to be problematical in some way. Consideration is then given to a fifth hypothesis which proposes that ovipositor length is constrained by abortion of syconia with relatively few seed embryos and many agaonid larvae. It is argued first that this pattern of abortion will be selected during a sustained period of heavy wasp infestation because seeds will then become scarce relative to pollen-carrying wasps. Increased expenditure by the fig on seed production would therefore be favoured by natural selection. A greater expenditure on seeds would occur if young syconia with exceptionally heavy wasp infestations were dropped and the saved nutrients invested in syconia of a subsequent crop containing average levels of wasp larvae and seeds. Provided that the energy and nutrient cost of dropping young syconia is small, the selective advantage to the wasp of longer ovipositors is eliminated in this way. A stable coexistence of figs and wasps is therefore possible. The paper concludes by discussing two general predictions of the abortion hypothesis, and how these may be tested.  相似文献   

16.
1. Figs on male dioecious fig trees (Ficus, Moraceae) are breeding sites for pollinator fig wasps (Hymenoptera, Agaonidae), but figs on female plants are traps that produce only seeds. As the short‐lived fig wasps cannot reproduce in female figs, natural selection should favour individuals that avoid them. Several studies have failed to detect such discrimination, a result attributed to inter‐sexual mimicry and ‘selection to rush’ in the wasps, but their experiments failed to explicitly take into account fig age (how long they had been waiting to be pollinated). 2. We compared the relative attraction of male and female figs of known ages of the South East Asian Ficus montana Burm. f. to its pollina tor Liporrhopalum tentacularis Grandi and examined how the reproductive success of the plant and its pollinator change with the age of the figs. 3. Mean retention time for un‐pollinated figs on female plants was 16 days whereas in male figs it was 12 days. Female figs remained attractive for up to 2 weeks, although the wasps were less willing to enter older figs. After pollinator entry, receptivity continued for several days, lasting longer in figs entered by a single wasp. Consistent with abortion rates, attractiveness persisted longer in female figs. Older figs produced fewer fig wasp offspring, but similar numbers of seeds. 4. The sexual differences in floral longevity in F. montana may represent part of a previously un‐recognised reproductive strategy in some fig trees that allows male plants to ‘export’ pollinators while also maintaining a resident fig wasp population.  相似文献   

17.
Abstract. Pollination of fig trees depends on mutualist wasps that reproduce within their flowers. Until recently, it was assumed that there was a short window of time during which a fig crop could be pollinated. Hence, pollination of figs was thought to depend on extreme efficiency of the wasps in locating receptive trees. In that context, extensive data on the Costa Rican fig tree Ficus pertusa L. have been very difficult to understand. In F. pertusa , figs of different crops attract wasps at different stages of their development. The crops that attract wasps the earliest in their development are the most heavily visited ones, but mature the fewest pollinator offspring and seeds on a per-fig basis. Using simulation models of pollinator population dynamics and field data, we show that (i) attractiveness of a crop is prolonged, (ii) wasps prefer large figs when given a choice, and (iii) the observed pattern of preferential early visitation of crops can be explained by temporal variations in pollinator abundance. This emphasizes the importance of population-level mechanisms to explain the fig/fig wasp mutualism.  相似文献   

18.
Fig-pollinating wasps lay their eggs in fig flowers. Some species of fig-pollinating wasps are active pollinators, while others passively transfer pollen. In dioecious fig species, the ovules of male figs produce wasps but no seeds. By observations and experiments on four dioecious Ficus species we show that (i) passive pollinators distribute pollen haphazardly within figs, but fertilization of female flowers in male figs is inhibited. Consequently, wasp larvae will develop in nonfertilized ovules: they cannot benefit from pollination; (ii) active pollinators efficiently fertilize flowers in which they oviposit. Lack of pollination increases larval mortality. Hence, fig pollinators are not obligate seed eaters but ovule gallers. Active pollination has probably evolved as a way to improve progeny nourishment.
Comparison of pollination and oviposition process in male and female figs, suggests that stigma shape and function have coevolved with pollination behaviour, in relation to constraints linked with dioecy.  相似文献   

19.
The host-specific relationship between fig trees (Ficus) and their pollinator wasps (Agaonidae) is a classic case of obligate mutualism. Pollinators reproduce within highly specialised inflorescences (figs) of fig trees that depend on the pollinator offspring for the dispersal of their pollen. About half of all fig trees are functionally dioecious, with separate male and female plants responsible for separate sexual functions. Pollen and the fig wasps that disperse it are produced within male figs, whereas female figs produce only seeds. Figs vary greatly in size between different species, with female flower numbers varying from tens to many thousands. Within species, the number of female flowers present in each fig is potentially a major determinant of the numbers of pollinator offspring and seeds produced. We recorded variation in female flower numbers within male and female figs of the dioecious Ficus montana growing under controlled conditions, and assessed the sources and consequences of inflorescence size variation for the reproductive success of the plants and their pollinator (Kradibia tentacularis). Female flower numbers varied greatly within and between plants, as did the reproductive success of the plants, and their pollinators. The numbers of pollinator offspring in male figs and seeds in female figs were positively correlated with female flower numbers, but the numbers of male flowers and a parasitoid of the pollinator were not. The significant variation in flower number among figs produced by different individuals growing under uniform conditions indicates that there is a genetic influence on inflorescence size and that this character may be subject to selection.  相似文献   

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