Floral biology, breeding system and pollination ecology of an endangered tree Tetracentron sinense Oliv. (Trochodendraceae)
© Gan et al.; licensee Springer. 2013
Received: 4 July 2013
Accepted: 21 October 2013
Published: 29 October 2013
Tetracentron sinense Oliv. is an endangered tree mainly distributed in south-central China. The breeding system and pollination ecology of T. sinense are unclear. With a conservation perspective, the floral biology, breeding system and pollination ecology of Tetracentron sinense Oliv. were investigated, in order to discuss the endangered factors related to pollination, and to provide important information for its conservation.
Our results revealed four important aspects of the reproductive biology of T. sinense. 1) T. sinense usually flowers by the beginning of June, and the flowering period of the population is about two months, and the florescence of florets lasted for 15 to 24 days with delicate fragrance. 2) The pollen/ovule ratio is 720 ± 28, and the outcrossing index is three. Artificial pollination experiments showed that T. sinense is self-compatible, with facultative xenogamy and no indication of agamospermy. 3) The pollination syndrome is ambophily, and self-pollination plays an important role in fruit production if wind and insect pollination is unavailable. 4) Insect pollinators were predominantly represented by Coleoptera, Diptera and Hymenoptera. Syrphid fly and bees were the main effective pollinators.
The results suggested that T. sinense exhibits a mixed-mating system, and autogamy in its breeding system may provide reproductive assurance for the population maintenance. During flowering and pollination in natural population, the decrease of population density and harsh environmental condition might be one of crucial reasons resulting in endanger for this species.
Information on the reproductive biology of endangered plants is crucial for predicting their survival capacity and suggesting the appropriate conservation measures (Rodriguez-Perez2005). Such studies may help to identify the factors affecting the reproduction of individual plants and the subsequent maintenance or regeneration of populations. A number of studies have suggested that the maintenance of plant populations is strongly influenced by both demographic (reproductive success) and genetic (inbreeding depression, evolutionary potential) mechanisms (Frankham & Ralls1998, Saccheri et al.1998). As determining the demographic and genetic crucial parameters, the breeding system lies at the very heart of population health and maintenance (Gaudeul & Till-Bottraud2004).
Pollination is an important link of successful plant reproduction, and is often dependent on mutualistic interactions with animals. A reduction in pollinator service can directly influence reproductive output, decreasing the quantity and/or quality of fruit and seed set and promoting selfing in self-compatible species (Rodriguez-Perez2005). In a broad sense, an increase in selfing rate would result in a reduction in gene flow within and/or among populations and thus cause an increase in inbreeding depression (Buza et al.2000). Many studies have suggested that rare plants exhibit slightly higher levels of self-compatibility than common plants (Saunders and Sedonia2006). Therefore, the inbreeding depression of a rare plant due to a lack of pollinator visits, is usually the most important factor resulting in endanger for the species.
Tetracentron sinense Oliv. is a deciduous tree with a catkin-like inflorescence, and placed in its own family, Tetracentraceae previously (Fu & Bartholomew2001), or more commonly in Trochodendraceae together with the monotypic Trochodendron (Martyn & Peter2007). This species is today mainly distributed in south-central China (Fu & Bartholomew2001), and scattered within a region 1100–3 500 m above sea level (Martyn & Peter2007). Due to its rarity and poor ability to regenerate naturally, it is considered 'rare’ according to the International Union for the Conservation of Nature (IUCN) (Fu1992). Since its vesselless wood is quite rare in angiosperm suggesting primitiveness, the species has received much taxonomic attention (Chen et al.2007, Angiosperm Phylogeny Group2009). However, studies on the reproductive biology of T. sinense are relatively scarce (Gan et al.2012). Until recently, little is known about the breeding system and pollination ecology of T. sinense, the most well known plants due to its economic importance.
In this paper, floral biology, breeding system and pollination ecology of an endangered tree T. sinense Oliv. were studied with a conservation perspective. The objective of this work was to deepen the understanding of the reproductive biology of T. sinense, and to identify the factors resulting in endanger during flowering and pollination, as well as to examine the implications of the results for its conservation.
Plant material and study site
Tetracentron sinense Oliv. is a deciduous tree to 40 m or more tall, with arching branches. Twigs are greyish-brown, with leaves alternate on the current shoot. Inflorescences are short pedunculate, with 80–125 sessile flowers. Flowers are yellowish green and hermaphrodite. Sepals 4 and are ovate-orbicular, but petals are absent. Stamens 4 and are exserted at anthesis, and then the filaments are subterete or slightly flattened. Anthers are dehiscent by a lateral slit. Styles 4 and are erect at first, and then become recurved and subulate at anthesis. Stigmas are along the ventral surface of the style.
The studies were conducted between April 2010 and October 2011 at the Longwo conservation station of Dafengding Natural Reserve, located in the northeast Meigu County, Sichuan Province, China (103°08′E, 28°46′N). The study site has an annual mean temperature of 9.6°C and received an annual mean rainfall of 1100 mm, and the relative humidity about 85%, and the pH of soil is acidic. The rainy season is from late June to October. The conservation station comprises a large population of T. sinense, with more than one hundred individuals scattered across from 2000 to 2400 meters above sea level, and the average inter-tree distance is 15 ± 6 m.
Phenology and floral biology
The time of anthesis initiation, and the blooming peak (months in which more than 50% of the individuals were in flower) and the termination in flowers were observed according to the methodology given in Dafni (1992). To describe the flowering period of an inflorescence and single flower, 40 inflorescences (4 inflorescences per tree) were tagged to study the time of anthesis additionally.
The floral biology was studied in 20 flowers from 10 inflorescences (one inflorescence per tree), revealing details such as morphological changes, anther dehiscence, nectar production, odor, and stigmatic status. For each flower, the pollen grains produced by two undehisced anthers were counted, and the average multiplied by the number of stamens. The ovules were counted after the dissection of ovaries under a stereoscopic microscope. The pollen–ovule ratio (P/O) and the outcrossing index (OCI) were calculated as recommended by Cruden (1977).
Pollen viability and stigma receptivity
Two flowers in different flowering stage were respectively sampled at random. The pollen viability was detected by MTT assay, and deeply/completely stained pollens were considered viable, according to Dafni (1992). The stigma receptivity was verified with the catalase activity method (Zeisler1938).
To determine the breeding system, pollination experiments were performed on randomly chosen from 10 trees in the population. On each plant, 4 to 10 inflorescences (depending on availability on each plant) were randomly tagged and only one of the treatments assigned to each inflorescence (i.e. to every single flower on that inflorescence). Inflorescences (n = 6 for each treatment) subjected to hand-pollination were bagged with thick waterproof paper bags before anthesis and bagged again after hand-pollination. The pollination bags were partly opened 5 days after each treatment to monitor fruit set. When required, the flowers were emasculated on the day of anthesis, before the anthers dehisced. The following treatments were conducted (Saunders and Sedonia,2006): (1) Control: the flowers were tagged and left to open pollination; (2) Geitonogamy: emasculated and bagged flowers were hand-pollinated using pollen from the same plant but from another flower (to test for self-compatibility); (3) Xenogamy: emasculated and bagged flowers were hand-pollinated using pollen from different plants (to test for outcrossing ability); (4) Cross-pollination under natural conditions: uncovered and emasculated flowers were pollinated freely (to test for pollen limitation); (5) Autogamy: flower buds were bagged and isolated from visitors (to test for autonomous self-pollination within a single flower); (6) Apomixis: flowers were bagged and emasculated before anthesis (to test for the agamospermy).
In addition, 1000 seeds for each treatment were weighed to determine the mean seed mass. To look for differences in germination among pollination treatments, a germination experiment using 100 randomly chosen seeds from each treatment was performed according to Luo et al. (2010).
Flower visitors were observed in the field over the peak of flowering in 2010 and 2011 on sunny days. Observations were made synchronously by several observers posted at three sites in the population from 0800 to 1800 every day, and were set periods (40 min). The pollinators and their behavior during the visits were observed and recorded, and used in conjunction with descriptions of floral morphology to evaluate their efficacy as pollinators. Representative floral visitors were collected and identified by specialists, and some of them were observed and photographed under a scanning electron microscopy for the presence and placement of T. sinense pollen (Saunders and Sedonia2006). These data, along with field observations, were used to ascertain which visitors were likely to be pollinators. T. sinense pollen was sufficiently distinct from synchronously flowering species that it could be distinguished on the insects with confidence. Voucher specimens of the insect visitors are deposited in the Herbarium of China West Normal University. Nearly 270 h of observation at the reserve was spent in the field watching flowers for floral visitors.
To determine the role of wind in pollination, glass microslides coated in sticky vaseline gel were tied vertically at 80 cm height in the canopy, and 2, 4, 6 and 8 m away from canopy of the isolated trees (n = 5) and scored after 24 h (Dafni1992). In addition, previously emasculated flowers (n = 200) were bagged with 1 mm2 plastic mesh to prevent the entry of insects and then monitored for fruit set. Some of these bagged flowers (n = 20) were removed after 24 h to determine the number of pollen grains deposited on the stigma as a result of wind.
The fruit setting, seed mass and germination rate among pollination treatments in artificial pollination experiment were analyzed with one-way ANOVAs followed by Duncan test using the statistic software SPSS 17.0.
Phenology and floral biology
Flower buds appeared at the end of April in this population. Flowering started by the beginning of June, and reached its maximum by the beginning of July, and finished at the beginning of August. Fruiting started 4 weeks after the commencement of blooming. Fruits became mature by the beginning of October. Thus, the flowering period of the population lasted for about two months, and fruiting period for about 3 months.
The green catkin-like inflorescences were produced near the base of the petiole, and sessile flowers with absent petals were laid in whorls of 4. The flowering period of an inflorescence lasted for about one month, and the lifespan of a single flower (from sepals opening to stamens lost) was 15–24 days. At the early stage of anthesis, the delicate fragrance from T. sinense flower was investigated, and then gradually weakened. The nectary is on the surface of ovary, and some flower-visiting insects were observed to stretch their mouthparts into the floral base for nectar.
Timing of pollen viability and stigma receptivity
The pollen viability and stigma receptivity of T. sinense
Developmental stage of flower
32.65 ± 1.91
30.63 ± 1.70
Stamens on the right and left of flower elongating
36.44 ± 2.71
Dehiscence of anthers on the right and left
62.47 ± 1.89
Stamens on the upper and lower of flower elongating
55.35 ± 2.64
Dehiscence of anthers on the upper and lower
47.02 ± 2.32
Pollen–ovule ratio (P/O) and the outcrossing index (OCI)
In a single flower of T. sinense, the pollen number is 18000 ± 706 (n = 20), and the ovule number is 25 ± 1 (n = 20), so the pollen-ovule ratio is 720 ± 28.
Diameter of inflorescence is 4.02 ±0.15 mm (n = 10) = 2;
Temporal separation between anther dehiscence and stigma receptivity: protogyny = 0; and
Stigma and anthers spatially separated: stamens are positioned higher than stigmas (stamens on the right and left of flower 1.82 ± 0.05 mm; stamens on the upper and lower of flower 0.86 ± 0.02 mm, n = 20) = 1.
The weight and germination rate of seed for T. sinense from three pollination treatments
Weight per 1000 seeds (mg)
90.70 ± 2.20a
76.80 ± 1.50b
81.60 ± 0.80b
Germination rate of seed (%)
Floral visitors and their rewards
Eristalis tenax Linnaeus
Syrphus vitripennis Meigen
Allograpta nigritibia Huo
Palumbia sinensis Curran
Xylocopa sinensis Smith
These insect visitors exhibited two kinds of different behavioral patterns. The species of Cerambycidae and Syrphidae often stayed on an inflorescence for about 1 min, when crawling and stretching their mouthparts into the flower base for foraging nectar. In contrast, the insects of Vespidae and Apidae usually flew around the inflorescence, and only stayed briefly to stretch their mouthparts into the flower base for foraging nectar, and then quickly flew to another inflorescence.
The visiting behavior of potential pollinators was significantly influenced by the external environmental factors, such as temperature (p = 0.019). On sunny days, the temperature was lower during the period of 0900 to 1040, when the visiting insects were rarely observed (7.13 ± 0.77 times). The visiting frequency of insects increased with the increase of temperature and illumination, and reached its peak (18.33 ± 3.76 times) from 1100 to 1340. Thereafter, the number of visiting insects reduced rapidly due to the decrease of temperature and illumination. Especially, almost no pollinator was observed after 1540 on sunny days, as well as on cloudy or rainy days.
The relationship between flowering and pollination
Our results suggest that the pollination syndrome of T. sinense is ambophily (pollination by both wind and insects). In pollination experiments, emasculated flowers bagged with plastic mesh set fruits, indicating T. sinense is wind-pollinated. Because inflorescences covered by paper bags did not set fruit, but did when hand-pollinated, the tree does not set fruits by apomixis. A lot of airborne pollen caught on the glass microslides also supports the effectiveness of wind pollination. The anemophilous floral features of T. sinense include the absence of petals, the papillate stigma, exposed anthers and stigma and elongated catkin-like inflorescences (Vikas2011; Yamasaki & Sakai2013). This species also appears to be insect-pollinated because insects with pollen on their bodies visited the flowers. As most of the pollen was observed on the mouthparts, chest and legs of flower visitors (Syrphid fly and bees), these insects may be effective pollinators. T. sinense exhibits floral characteristics that are adapted to insect pollination: (1) the floral traits such as herkogamy, protogyny and the recurved styles, are all helpful for insect-pollination (Mayer et al.2011); (2) The inflorescences with many closely ranked and sessile flowers are beneficial for insect visitors to stay for a long time; (3) The anthesis of a single flower is longer (lasted for 15 to 24 days), and the time of releasing pollen for the stamens of T. sinense flower is relatively concentrated; (4) In the population, the blossom is relatively concentrated in July, and the delicate fragrance and nectary were investigated during anthesis, which can provide important visiting reward as pollen and nectar for insect visitors (Dafni1992, Yamasaki & Sakai2013).
The extent of ambophily in angiosperms has been recently reviewed by Culley et al. (2002). Relatively few flowering plants show ambophily (pollination by both wind and insects) (Yamasaki & Sakai2013). Generally, ambophily is considered an intermediate condition during a transition to either full wind pollination or biotic pollination (Culley et al.2002). In some pioneer plants (including Salix spp. and Azadirachta indica), ambophily is advantageous because of changing wind conditions during forest succession (Karrenberg et al.2002, Vikas2011). In other plants (for example, Mallotus japonicus), the decrease of population density also contribute to the maintenance of ambophily (Yamasaki & Sakai2013). Previous studies have reported that in wind-pollinated plants, pollen limitation increases rapidly with the increases in distance from a pollen source (Hesse & Pannell2011). In contrast, pollen limitation does not strongly depend on distance from a pollen source in insect-pollinated plants (Albrecht et al.2009). As been extensively deforested in history resulting in the decrease of its population density, at present most T. sinense sporadiclly scatter in the mountains, valleys, stream or steep cliffs (Fu1992). In the population, the distance between individuals is 15 ± 6 m, larger than the average traveling distance (8 m) of airborne pollens, and the amount of airborne pollen rapidly decreased with distance from the pollen source, resulting in the increase of pollen limitation from wind pollination. Therefore, the entomophilous characteristic of T. sinense may remedy the pollen limitation from wind pollination, which is an adaptive strategy for T. sinense to assure the reproduction success. So we think the maintenance of ambophily in T. sinense should attribute to the decrease of population density.
In this study, fruits were produced after the autogamy treaments, suggesting T. sinense is autonomously self-pollinated. T. sinense also exhibits several floral traits specially associated with self-pollination: bisexual flower, the recurved style positioned lower than the anthers, protogyny, no temporal separation between pollen viability and stigma receptivity (Faegri & van der Pijl1979). However, the fruit set, seed mass and germinate rate from autogamy are significantly lower than that from xenogamy and control. In addition, pollination experiments showed that fruit set of T. sinense in natural population was limited by pollinators, and there is no agamospermy. So we conclude that autonomous self-pollination plays an important role in fruit production if wind- and insect-pollination is unavailable.
Breeding system and its adaptability
Artificial pollination experiments showed that T. sinense is self-compatible and outcrossing fertile, and no apomixes is occurred. The fruit set from xenogamy is higher than that from control and cross-pollination under natural conditions, indicating the pollinator limitation in natural population. The results showed that T. sinense is self-compatible, and sometimes needs pollination vector, and can be pollinated by wind and insect (Syrphid fly and bees), which is in accordance with that from out-crossing index and pollen-ovule ratio. According to Dafni (1992), the out-crossing index is 3, indicating T. sinense is self-compatible, with facultative xenogamy, and sometimes needs pollinators. The pollen-ovule ratio (720 ± 28) belongs to the range of 244.7-2588.0 corresponding to the values reported for facultative xenogamy (Cruden1977). Therefore, the mating system of T. sinense is mixed with self-pollination and out-crossing, and there is no apomixes. While, the fruit set from xenogamy and control is respectively higher 25.87% and 18.43% than that from autogamy, and the seed germination rate from autogamy is respectively lower 56.43% and 32.35% than that from xenogamy and control, suggesting that outcrossing predominated in the breeding system of T. sinense.
Evolution of plant mating strategies always has one main theme related to the evolution of cross- versus self-fertilization (Barrett1998). The evolutionary pathway from obligate outcrossing based on self-incompatibility to predominant self-fertilization has possibly been followed by more different lines of evolution in flowering plants than any others (Stebbins1974). It was predicted that predominant selfing and predominant outcrossing should be alternative stable outcomes of mating system evolution in most plant population (Lande and Schemske1985), which was be validated by the existence of some species with stable, mixed mating-systems in natural plant populations (Barrett and Harder1996). Our results showed that in the mating system of T. sinense existed both selfing and outcrossing simultaneously. However outcrossing predominated in T. sinense, and autonomous self-pollination just played an assistant role to assure production in the breeding system, when conditions for outcrossing are unfavorable, such as shift of environment conditions, or the normal pollinators are missing or reduced in abundance (Huang et al.2006).
Factors resulting in endanger during flowering and pollination
Despite the occurrence of successful insect pollination, the pollinator activity is easily influenced by environmental condition, and almost no visiting insect was observed on rainy or cloudy days in this study. In Meigu Dafengding Natural Reserve, the flowering period of T. sinense is just coincident with the rainy season (June to August), which has a negative impact on the flower-visiting behavior of insects. In addition, the density of airborne pollen grains declined completely 8 m away from the canopy, and the average inter-tree distance is 15 ± 6 m due to the decrease of population density, which may have a negative effect on wind-pollination for this species. Thus, the successful reproduction for T. sinense may only rely on self-pollination or geitonogamy in most cases, which would result in autogamous and geitonogamous selfing. However, selfing would result in inbreeding depression or reduction of genetic diversity, and then decreasing the ability of the population to adapt in response to environmental change (Buza et al.2000, Gaudeul & Till-Bottraud2003), which would be unfavorable to natural regeneration of T. sinense. Thereby, the decrease of population density and harsh environmental condition during flowering and pollination might be one of crucial reasons resulting in endanger for this species. The urgent task is to comprehensively analyze the factors resulting in poor ability to regenerate naturally during genetic and developmental process of T. sinense, and to formulate effective protective measures. Especially, it is necessary to enlarge its population and individual number as soon as possible through artificial intervention.
In summary, we investigated the floral biology, breeding system and pollination ecology of Tetracentron sinense Oliv. The occurrence of successful wind and insect pollination indicates that T. sinense is ambophilous, and the maintenance of ambophily may attribute to the decrease of population density. The breeding system of T. sinense is mixed with self-pollination and out-crossing, with no indication of agamospermy. Outcrossing predominated in the mating system, and autonomous self-pollination in its breeding system may provide reproductive assurance for the population maintenance. During flowering and pollination in natural population of Tetracentron sinense, the decrease of population density and harsh environmental condition might be one of crucial reasons resulting in endanger for this species.
We thank all students who help to collecting and analyzing data: Yongshen Pan, Li Zhao, and Wenfeng Lan. We are grateful to Jingting Li and Keke Huo from for insect identification respectively. This work was supported by National Natural science Foundation of China (NO.31370367) and the key fund of natural science of education department, Sichuan Province, China (No.12ZA169).
- Albrecht M, Duell P, Obrist MK, et al.: Effective long distance pollen dispersal in Centaurea jacea . PLoS ONE 2009, 4: e6751. 10.1371/journal.pone.0006751PubMed CentralView ArticlePubMedGoogle Scholar
- Angiosperm Phylogeny Group: An update of the angiosperm phylogeny group classification for the orders and families of flowering plants: APG III. Botanical Journal of the Linnean Society 2009, 161: 105–121.View ArticleGoogle Scholar
- Barrett SCH: The evolution of mating strategies in flowering plants. Trends in Plant Science 1998, 3: 335–341. Barrett 1998 Barrett 1998 10.1016/S1360-1385(98)01299-0View ArticleGoogle Scholar
- Barrett SCH, Harder LD: Ecology and evolution of plant mating. Trends in Ecology and Evolution 1996, 11: 73–79. 10.1016/0169-5347(96)81046-9View ArticlePubMedGoogle Scholar
- Buza L, Young A, Thrall P: Genetic erosion, inbreeding and reduced fitness in fragmented populations of the endangered tetraploid pea Swainsona recta . Biological Conservation 2000, 93: 177–186. 10.1016/S0006-3207(99)00150-0View ArticleGoogle Scholar
- Chen L, Ren Y, Endress PK, et al.: Floral organogenesis in Tetracentron sinense (Trochodendraceae) and its systematic significance. Plant Systematic and Evolution 2007, 264: 183–193. 10.1007/s00606-006-0505-yView ArticleGoogle Scholar
- Cruden RW: Pollen ovule ratios: A conservative indicator of breeding systems in flowering plants. Evolution 1977,31(1):32–46. 10.2307/2407542View ArticleGoogle Scholar
- Culley TM, Weller SG, Sakai AK: The evolution of wind pollination in angiosperms. Trends in Ecology &and Evolution 2002, 17: 361–369. 10.1016/S0169-5347(02)02540-5View ArticleGoogle Scholar
- Dafni A: Pollination Ecology. New York: Oxford University Press; 1992:1–57.Google Scholar
- Faegri K, van der Pijl L: The principles of pollination ecology. 3rd edition. Rev. New York: Pergamon Press; 1979.Google Scholar
- Frankham R, Ralls K: Inbreeding leads to extinction. Nature 1998, 392: 441–442. 10.1038/33022View ArticleGoogle Scholar
- Fu LG: Plant red book in China—rare and endangered plants (Book I).Beijing. Beijing: China Science Press; 1992:452–453. 682–683 682–683Google Scholar
- Fu DZ, Bartholomew B: Tetracentron in Wu ZY and Raven P H. Flora of China, 6: 125. Beijing: Science Press and Missouri Botanical Garden Press; 2001.Google Scholar
- Gan XH, Xie D, Cao LL: Sporogenesis and development of gametophytes in an endangered plant, Tetracentron sinense Oliv. Biological Research 2012,45(4):393–398. 10.4067/S0716-97602012000400011View ArticlePubMedGoogle Scholar
- Gaudeul M, Till-Bottraud I: Low selfing rate in an endangered perennial plant, Eryngium alpinum L. American Journal of Botany 2003, 90: 716–723. 10.3732/ajb.90.5.716View ArticlePubMedGoogle Scholar
- Gaudeul M, Till-Bottraud I: Reproductive Eecology of the Eendangered Aalpine Species Eryngium alpinum L. (Apiaceae): Pphenology, Ggene Ddispersal and Rreproductive Ssuccess. Annals of Botany 2004, 93: 711–721. 10.1093/aob/mch098PubMed CentralView ArticlePubMedGoogle Scholar
- Hesse E, Pannell JR: Density-dependent pollen limitation and reproductive assurance in a wind-pollinated herb with contrasting sexual systems. Journal of Ecology 2011, 99: 1531–1539. 10.1111/j.1365-2745.2011.01880.xView ArticleGoogle Scholar
- Huang Y, Zhang CQ, Blackmore S, et al.: A preliminary study on pollination biology of Omphalogramma souliei Franch. (Primulaceae), a species endemic to China. Plant. Systematic. Evoluation. 2006, 261: 89–98. 10.1007/s00606-006-0430-0View ArticleGoogle Scholar
- Karrenberg S, Kollmann J, Edwards PJ: Pollen vectors and inflorescence morphology in four species of Salix . Plant Systematic and Evolution 2002, 235: 181–188. 10.1007/s00606-002-0231-zView ArticleGoogle Scholar
- Lande R, Schemske DW: The evolution of self-fertilization and inbreeding depression. Genetic models. Evolution 1985, 39: 24–40. 10.2307/2408514View ArticleGoogle Scholar
- Luo JD, Gan XH, Jia XJ, et al.: Biological characteristic of seeds of endangered plant Tetracentron sinense (Tetracentraceae). Acta Botanica Yunnanica 2010,32(3):204–210. 10.3724/SP.J.1143.2010.09233View ArticleGoogle Scholar
- Martyn R, Peter C: Tetracentron sinense. Kew: The Board of Trustees of the Royal Botanic Gardens; 2007:168–173.Google Scholar
- Mayer C, Adler L, Armbruster WS, et al.: Pollination ecology in the 21st century: key questions for future research. Journal of Pollination Ecology 2011,3(2):8–23.Google Scholar
- Rodriguez-Perez J: Breeding system, flower visitors and seedling survival of two endangered species of Helianthemum (Cistaceae). Ann Bot 2005, 95: 1229–1236. 10.1093/aob/mci137PubMed CentralView ArticlePubMedGoogle Scholar
- Saccheri I, Kuussaari M, Kankare M, et al.: Inbreeding and extinction in a butterfly metapopulation. Nature 1998, 392: 491–494. 10.1038/33136View ArticleGoogle Scholar
- Saunders NE, Sedonia DS: Reproductive biology and pollination ecology of the rare Yellowstone Park endemic Abronia ammophila (Nyctaginaceae). Plant Species Biology 2006, 21: 75–84. 10.1111/j.1442-1984.2006.00153.xView ArticleGoogle Scholar
- Stebbins GL: Flowering plants: evolution above the species level. Cambridge, Massachusetts: Belknap Press; 1974:15.View ArticleGoogle Scholar
- Vikas TR: Reproductive biology of Azadirachta indica (Meliaceae), a medicinal tree species from arid zones. Plant Species Biology 2011, 26: 116–123. 10.1111/j.1442-1984.2010.00311.xView ArticleGoogle Scholar
- Yamasaki E, Sakai S: Wind and insect pollination (ambophily) of Mallotus spp. (Euphorbiaceae) in tropical and temperate forests. Aust J Bot 2013, 61: 60–66. 10.1071/BT12202View ArticleGoogle Scholar
- Zeisler M: Über die Abgrenzung der eigentlichen Narbenflä che mit Hilfe von Reaktionen. Beihefte zum Botanischen Central Blatt 1938, 58: 308–318.Google Scholar
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