野牡丹科植物与蜂类某些类群的进化关系初探

本文提出熊蜂、胡蜂等采集野牡丹科植物花粉的现象,进而探讨了野牡丹科植物与熊蜂、胡蜂……等之间的共同进化关系,并指出野牡丹科植物与熊蜂等类群,在系统进化中有平行进化的关系。     

熊蜂携带花粉的电镜鉴定及与采访植物协同演化关系的研究

通过对蜜蜂总科（Apoidea）熊蜂属Bombus15个亚属、20种的熊蜂蜂王花粉篮中携带的花粉进行电镜扫描鉴定,结果结合熊蜂及植物比较形态学、熊蜂亚属及采访植物间进化关系进行了分析。结果表明：熊蜂的采访植物包括被子植物的9目、10科,涉及原始、进化及中间3种植物类型,且颚眼距较长的熊蜂亚属既采访长管花也采访短管花植物,颚眼距较短的熊蜂亚属则只倾向于采访短管花植物。     

广东大雾岭自然保护区野牡丹科植物资源调查与鉴定研究

对大雾岭自然保护区的野牡丹科植物资源进行了初步调查。依照《广东植物志》分类方法进行鉴定,调查结果为:大雾岭野牡丹科植物有野牡丹属、锦香草属和虎颜花属共三个属的5种,1个亚种。另外还发现一种植物特征与毛菍类似但叶片为7基出脉的植物,有待于进一步确定其归属。本次调查为野牡丹科植物野生资源的保护和科学利用提供了资料。     

华北地区六种熊蜂的地理分布及生态习性

2005～2007年连续3年对华北地区小峰熊蜂Bombus hypocrita、密林熊蜂B.patagiatus、红光熊蜂B.ignitus、明亮熊蜂B.lucorum、火红熊蜂B.pyrosoma和重黄熊蜂B.picipes等6种熊蜂的地理分布和生态习性进行研究。结果表明,这6种熊蜂在华北地区的地理分布差异很大,火红熊蜂分布最广,重黄熊蜂分布最窄。6种熊蜂在垂直分布上也存在差异,红光熊蜂分布于较低海拔高度地区,明亮熊蜂分布于较高海拔高度地区,但在海拔1300～1800m范围内6种熊蜂都有分布。6种熊蜂中,火红熊蜂的年活动周期较长,为180天左右。小峰熊蜂、明亮熊蜂、密林熊蜂和重黄熊蜂的年活动周期居中。红光熊蜂的年活动周期最短,为140天左右。6种熊蜂采访植物涉及到17科63种,采访植物存在一定的偏好性,主要采访豆科、菊科、蔷薇科和唇形科等植物;而且,不同种熊蜂采集植物的种类也存在较大差异。     

封面照片:红光熊蜂Bombus ignitus Smith

熊蜂是一类重要的传粉昆虫,隶属于膜翅目Hymenoptera蜜蜂科Apidae熊蜂属Bombus,目前,全世界已知熊蜂种类约250种,中国约108种。熊蜂具有进化程度低、趋光性差、耐低温等生物学特性,适应温室环境能力强,因此,熊蜂属中一些易于人工驯养的种类被逐渐开发出来,并提供温室果菜传粉应用,取得了良好的经济效益和生态效益。     

10种野牡丹科植物引种栽培及应用研究

通过对广州地区6个野牡丹科植物野生种及国外引进4个园艺栽培种进行物候学、抗寒性系统观察,综合评价观赏价值和适应性后对其打分,筛选出7个野牡丹科植物可大规模应用于广州及周边地区园林绿化,丰富了本市园林植物品种种类。     

蜜蜂及熊蜂微孢子虫rRNA基因研究

核糖体RNA(rRNA)是一种理想的进化计时器,已广泛地应用于研究微生物的系统发育和进化关系。蜜蜂和熊蜂都被微孢子虫感染,关于蜜蜂和熊蜂微孢子虫rRNA基因研究主要有rRNA基因序列的测定分析、二级结构的研究和用rRNA基因检测诊断微孢子虫等。这些对蜜蜂和熊蜂微孢子虫系统发育的研究和微孢子虫的防治等具有重要的推动作用。     

《群居性昆虫:级的进化途径及繁殖》

本书讨论了群居性昆虫的繁殖及其重要的调节机理,提出了激素和性外激素在群居性昆虫级的发育中的作用,各种级别的功能,并阐述了繁殖差异的生理基础与群居生物学方面的关系,以及不同级别在群体内自动平衡的微妙调节机能等。全书264页。目次：1．昆虫级的进化,2．昆虫级的概念Z3．白蚁性的级别及繁殖策略;4．蚂蚁的工以与以后形成的调节及群落发展;5．胡蜂的生理与繁殖;6．隧蜂科的繁殖和级;7．木蜂科的级;已熊蜂的级和繁殖Zg．蜜蜂及无刺蜂级的发展繁殖策略和生产力的控制;10．蜜蜂王蜂的生殖生理和习性的差异性;！1．真群居性…     

野牡丹科十属植物研究进展

本文综述了野牡丹科十属植物的化学成分、生物活性以及临床应用等内容,是对该科属植物近40多年来相关研究的首次较系统的归纳总结,为相关植物的进一步研究和开发利用提供参考.     

马先蒿属花冠形态的多样性与传粉式样的关系

马先蒿属(Pediculais)是有花植物中花冠形态多样化最为集中的属。该属主要的传粉者是熊蜂属(Bormbus)昆虫;在北美,熊蜂和蜂鸟是马先蒿植物一些种类有效的传粉者;也发现壁蜂(Osmia)为其传粉。不同的传粉机制要求某一特定的取食式样储藏和释放花粉。本文讨论了花冠类型的进化趋势与传粉式样和花粉形态的关系。传粉者的选择压力是决定花冠多样化的重要因素之一;花冠类型与传粉者和传粉行为紧密相关。马先蒿植物和传粉者的相互依赖与其花冠类型、功能和物候互相适应,但花冠类型与花粉形态两者之间似乎没有明显的一一对应关系。通过北美、日本和喜马拉雅不同地理分布马先蒿种类的比较研究表明,具有相同花冠类型的种类有着相同的传粉方式,花冠形态与传粉式样存在紧密的协同进化关系。     

Molecular phylogenetics of Melastomataceae and Memecylaceae: implications for character evolution

Melastomataceae are among the most abundant and diversified groups of plants throughout the tropics, but their intrafamily relationships and morphological evolution are poorly understood. Here we report the results of parsimony and maximum likelihood (ML) analyses of cpDNA sequences from the rbcL and ndhF genes and the rpl16 intron, generated for eight outgroups (Crypteroniaceae, Alzateaceae, Rhynchocalycaceae, Oliniaceae, Penaeaceae, Myrtaceae, and Onagraceae) and 54 species of melastomes. The sample represents 42 of the family's currently recognized ～150 genera, the 13 traditional tribes, and the three subfamilies, Astronioideae, Melastomatoideae, and Memecyloideae (= Memecylaceae DC.). Parsimony and ML yield congruent topologies that place Memecylaceae as sister to Melastomataceae. Pternandra, a Southeast Asian genus of 15 species of which five were sampled, is the first- branching Melastomataceae. This placement has low bootstrap support (72%), but agrees with morphological treatments that placed Pternandra in Melastomatacaeae because of its acrodromal leaf venation, usually ranked as a tribe or subfamily. The interxylary phloem islands found in Memecylaceae and Pternandra, but not most other Melastomataceae, likely evolved in parallel because Pternandra resembles Melastomataceae in its other wood characters. A newly discovered plesiomorphic character in Pternandra, also present in Memecylaceae, is a fibrous anther endothecium. Higher Melastomataceae lack an endothecium as do the closest relatives of Melastomataceae and Memecylaceae. The next deepest split is between Astronieae, with anthers opening by slits, and all remaining Melastomataceae, which have anthers opening by pores. Within the latter, several generic groups, corresponding to traditional tribes, receive solid statistical support, but relationships among them, with one exception, are different from anything predicted on the basis of morphological data. Thus, Miconieae and Merianieae are sister groups, and both are sister to a trichotomy of Bertolonieae, Microlicieae + Melastomeae, and Dissochaeteae + Blakeeae. Sonerileae/Oxysporeae are nested within Dissochaeteae, Rhexieae within Melastomeae, and African and Asian Melastomeae within neotropical Melastomeae. These findings have profound implications for our understanding of melastome morphological evolution (and biogeography), implying, for example, that berries evolved from capsules minimally four times, stamen connectives went from dorsally enlarged to basal/ventrally enlarged, and loss of an endothecium preceded poricidal dehiscence.     

Functional morphology of the visual system and mating strategies in bumblebees (Hymenoptera,Apidae, Bombus)

Bumblebee mating behaviour intrigued Darwin over 150 years ago and has elicited much interest since. Despite our increasing knowledge about male mating strategies, we still know little about the signals and cues involved, the sender‐receiver relationship and the functional adaptations of the involved sensory systems. Although several authors have noticed a close relationship between the mating system and male‐specific elaboration of the visual system, studies on the functional adaptations have yet to be conducted. We investigated the functional morphology of the compound eyes in 11 species of Bombus from various subgenera in detail. Of these, four species (Bombus confusus, Bombus melaleucus, Bombus mendax, Bombus niveatus) have enlarged male eyes, characterized by a higher number of ommatidia compared with worker eyes and a frontal zone with enlarged facets, which is likely to be associated with improved spatial resolution and contrast sensitivity. In these species, perching mating strategies are found. In contrast, males of species that patrol scent routes (Bombus hortorum, Bombus lapidarius, Bombus pascuorum, Bombus pratorum, Bombus soroeensis, Bombus terrestris, Bombus wurflenii) show no distinct eye adaptations, and their eye morphology closely resembles that of the workers. A phylogenetic analysis of male eye structure indicates that enlarged males eyes may have been the ancestral state in Bombus. © 2014 The Linnean Society of London     

Aluminium accumulation in leaves of 127 species in Melastomataceae,with comments on the order Myrtales

The distribution and systematic significance of aluminium accumulation is surveyed based on semi-quantitative tests of 166 species, representing all tribes and subfamilies of the Melastomataceae as well as a few members of related families within the Myrtales. The character is strongly present in nearly all members of the Memecylaceae and in most primitive taxa of the Melastomataceae, while non-accumulating taxa are widespread in the more derived tribes of the Melastomataceae. The variable distribution of Al accumulation in advanced clades of the latter family is probably associated with the tendency to herbaceousness, although it is unclear whether the more herbaceous representatives have developed more specialized Al-response mechanisms that may exclude high Al levels from the shoot. It is hypothesized that Al accumulation is symplesiomorphic for Melastomataceae and Memecylaceae, and that the feature characterizes the most primitive families in the Myrtales. Indeed, Al accumulation is also characteristic of Crypteroniaceae, Rhynchocalycaceae and Vochysiaceae. Crypteroniaceae and Rhynchocalycaceae probably take a basal position in a sister clade of the Memecylaceae and Melastomataceae, while Al accumulation suggests a basal position for Vochysiaceae in the Myrtaceae clade.     

Cytological variation and pathogenicity of the bumble bee parasite Nosema bombi (Microspora, Nosematidae)

In three field seasons, 2003-2005, bumble bees were collected in southern Sweden and eastern Denmark in search of microsporidian parasites. Of the 16 bumble bee species studied, microsporidia were found in Bombus hortorum, Bombus hypnorum, Bombus lapidarius, Bombus lucorum, Bombus pascuorum, Bombus pratorum, Bombus ruderarius, Bombus subterraneus and Bombus terrestris. Only one microsporidian species, Nosema bombi, was recorded. A microsporidium found in B. pratorum differed cytologically from microsporidia of the other host species. In the most frequently infected host, B. terrestris, the prevalence was 20.6%. Totally 1049 specimens were dissected. The light microscopic and ultrastructural cytology and pathology of N. bombi is described with focus on the variation recorded. Variation was especially prominent in the shape, size and coupling of spores, and in the length and arrangement of the polar filament. In four host species microsporidian infection was restricted to peripheral fat cells.     

Distribution and Diversity of Pteridophytes and Melastomataceae along Edaphic Gradients in Yasuní National Park, Ecuadorian Amazonia1

We documented the floristic composition of pteridophytes (ferns and fern allies) and Melastomataceae in Yasuní National Park, Amazonian Ecuador. Our main questions were: (1) Are the density of individuals, species richness, and/or species diversity (measured with Shannon's H′) of the two plant groups related to edaphic differences? and (2) How many of the pteridophyte and Melastomataceae species are non–randomly distributed in relation to a soil base content gradient within terra firme (non–inundated forest). To answer these questions, we sampled 27 line transects of 500 × 5 m distributed in an area of ca 20 × 25 km. The study area included a permanent 50 ha plot established to monitor forest dynamics; thus, our results also provide information on landscape–scale floristic variability to which results from within the plot can be compared. A total of 45,608 individuals and 140 species of pteridophytes, and 4893 individuals and 89 species of the Melastomataceae, were counted in the transects. Both with pteridophytes and with Melastomataceae, a clear negative correlation was found between the amount of extractable bases in the soil and the number of plant individuals encountered in a transect. With Melastomataceae, species richness and species diversity also were negatively correlated with soil base content, but with pteridophytes they were not. More than 50 percent of the common species of both pteridophytes and Melastomataceae were nonrandomly distributed along the soil cation content gradient within terra firme. We conclude that while the species richness patterns observed in one plant group are not indicative of similar patterns in other plant groups, it seems likely that a substantial (but unknown) proportion of species belonging to other plant groups will be found to show distribution patterns that reflect edaphic preferences within terra firme forests.     

A new species, Memecylon mundanthuraianum, of Melastomataceae from India

A new species of Melastomataceae, Memecylon mundanthuraianum , is described here with illustrations from the Kalakkad-Mundanthurai Tiger Reserve of Tamil Nadu, India.     

Phylogeny and circumscription of the near-endemic Brazilian tribe Microlicieae (Melastomataceae)

The members of tribe Microlicieae in the flowering plant family Melastomataceae are nearly all endemic to the cerrado biome of Brazil. Traditional classifications of the Melastomataceae have attributed between 15 and 17 genera to the Microlicieae, but subsequent revisions have circumscribed the tribe more narrowly. The monophyly and intergeneric relationships of the Microlicieae were evaluated through phylogenetic analyses with molecular and morphological data sets. Incorporation of DNA sequences from the intron of the chloroplast gene rpl16 into a previously generated family-wide data set yielded a clade comprising Chaetostoma, Lavoisiera, Microlicia, Rhynchanthera, Stenodon, and Trembleya ("core Microlicieae"), with Rhynchanthera as the first-diverging lineage. The other four genera of Microlicieae sampled are placed in other clades: Eriocnema with Miconieae; Siphanthera with Aciotis, Nepsera, and Acisanthera of Melastomeae; Castratella as sister to Monochaetum of Melastomeae; and Cambessedesia as part of an unresolved polytomy in a large clade that includes most Melastomataceae. Analyses of the chloroplast genes rbcL and ndhF that included three core genera produced similar results, as did the combined analysis of all three data sets. Combined parsimony analyses of DNA sequences from rpl16 and the nuclear ribosomal intercistronic transcribed spacer (ITS) region of 22 species of core Microlicieae yielded generally low internal support values. Lavoisiera, recently redefined on the basis of several morphological characters, was strongly supported as monophyletic. A morphological phylogenetic analysis of the Microlicieae based on 10 parsimony-informative characters recovered a monophyletic core Microlicieae but provided no further resolution among genera. Penalized likelihood analysis with two calibration time windows produced an age estimate of 3.7 million years for the time of initial divergence of strictly Brazilian core Microlicieae. This date is in general agreement with the estimated age of the most active stage of development of cerrado vegetation and implies an adaptive shift from hydric to seasonally dry habitats during the early evolution of this group.     

Ferns and Melastomataceae as indicators of vascular plant composition in rain forests of Colombian Amazonia

In a case-study from Colombian Amazonia, species information from ferns and Melastomataceae was used to explain the compositional patterns of other vascular plant species in 40 widely distributed 0.1-ha plots. Canonical correspondence analysis was applied to regress vascular plant species composition in the forests against information from these two indicator groups (summarized as axes of principal coordinate analyses), together with that from soils, landscape, and the spatial sampling design. In total, 53,941 individuals of 2480 vascular plant species were recorded. Of these, 17,473 individuals and 132 species were from ferns and Melastomataceae. In 19 well-drained upland (tierra firme) plots 19,622 vascular plant individuals and 1716 species were found, with 3793 plants and 91 species from ferns and Melastomataceae. In both the set of all landscapes and the subset of tierra firme forests the principal PCoA axes of the two indicator groups were highly related to the main patterns of forest species composition. In principle, therefore, ferns and Melastomataceae can be used to detect and forecast changes in the forest composition of the study area. However, evidence was not obtained that ferns and Melastomataceae show more potential to predict the main patterns in species composition of forests than soil, landscape, and spatial variables. The partioning of the total variation in forest composition showed that the correlation of ferns and Melastomataceae with other forest plants was quite independent from that of soil, landscape, and space. Direct effects of ferns and Melastomataceae on other plants might be obtained from experimental studies of between-plant interactions, concentrating on the seedling or juvenile stages of trees and lianas, both above-ground as well as in the rooting environment.     

火红熊蜂微卫星标记的筛选及种特异性分析

火红熊蜂Bombus pyrosoma是中国特有的熊蜂资源, 在华北地区分布十分丰富, 是众多野生植物和农作物的重要传粉者。为了探究火红熊蜂的遗传结构及其进化关系, 首次开展了该种熊蜂卫星标记的筛选及其种特异性研究。本研究采用生物素-磁珠吸附分离法从火红熊蜂基因组中筛选微卫星标记, 并选取黑熊蜂亚属Melanobombus其他7种熊蜂进行了这些标记的种特异性验证。结果表明： 不同探针与磁珠杂交产生的微卫星标记阳性克隆率存在很大差异, TC探针的微卫星阳性克隆率最高为82%; TG探针次之, 为28%; AT和GC探针分离未获得微卫星标记克隆。根据获得的阳性克隆的序列设计引物进行筛选验证, 共获得31对熊蜂微卫星序列特异性引物。微卫星标记分析发现, 完美型(perfect)18个, 占58.1%; 非完美型(imperfect)10个, 占32.3%; 混合完美型(compound perfect)1个, 占3.2%; 混合非完美型(compound imperfect)2个, 占6.4%。不同探针的微卫星核心序列重复数不同, TC探针和TG探针的微卫星核心序列最高重复数分别为28和15个, 最低重复数分别为7和11个。利用所获得的31对微卫星引物对黑熊蜂亚属其他7种熊蜂进行检测, 有26对引物可以扩增所测试的7种熊蜂, 其他5对引物只能扩增部分熊蜂种类, 其中BPM5是火红熊蜂种特异性引物。本研究从火红熊蜂基因组中筛选的微卫星标记, 不仅可用于火红熊蜂的遗传结构、 分子进化和资源保护等方面的研究, 而且可进一步用于黑熊蜂亚属其他种群的遗传特性分析。