J Syst Evol ›› 2017, Vol. 55 ›› Issue (1): 44-53.doi: 10.1111/jse.12210

• Research Articles • Previous Articles     Next Articles

Temporal variation in relative frequency of nectariferous and nectarless inflorescences and its effect on subsequent fecundity in an ephemeral plant, Corydalis ambigua (Fumariaceae)

Xing-Nan Zhao1, Ji-Min Zhao2, Ji-Xun Guo1*, and Yan-Wen Zhang1,2,3*   

  1. 1Institute of Grassland Science, Northeast Normal University and Key Laboratory for Vegetation Ecology, Ministry of Education, Changchun 130024, China
    2Department of Biology, Changchun Normal University, Changchun 130032, China
    3Department of Biology, Eastern Liaoning University, Dandong 180003, Liaoning, China
  • Received:2016-01-20 Online:2016-05-13 Published:2017-01-12

Abstract: The occurrence of nectarlessness flowers in nectar-producing plants is a common and stable phenomenon in many species, but their occurrence is still not well understood. The aim of this study is to examine a question from both the plant and pollinator perspectives: why do nectar-producing species produce some nectarless flowers within a plant? We investigate the distribution patterns of nectarless flowers in natural populations and their variation among the populations and years in a spring-flowering self-incompatible perennial herb plant, Corydalis ambigua Chem. & Schlecht (Fumariaceae), we observed the foraging behavior of bumblebees to nectariferous and nectarless inflorescences. We also examined the differences in reproductive success between inflorescence types and the effect of nectar production on flower production of the next flowering season. The results indicated that the frequencies of nectarless flowers varied among inflorescences, individuals, and populations and between years. Plants can revise or keep their inflorescence types or change nectar production status in the next growing season. Bumblebees visited both types with equal frequency but different foraging behavior, which resulted in lower seed production in nectarless inflorescences. However, nectarless inflorescences may save more energy and result in larger bulbs, which produce more flowers in the next flowering season. We found that although nectarless flowers resulted in lower seed set in nectarless inflorescence or individuals, they could affect bumblebees’ foraging behavior and further promote the effective output of pollen. In addition, the resource savings could enhance plant reproductive success in the next flowering season.

Key words: Bombus, bumblebee, Corydalis ambigua, cost of reproduction, foraging behavior, nectarless flower, reproductive strategy

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[1] Ruhai Li1, 2, 3, Sheng Qiang1*. Application of Cryo-sectioning Technique in Weed Fruits[J]. Chin Bull Bot, 2010, 45(06): 739 -743 .
[2] . [J]. Chin Bull Bot, 1994, 11(专辑): 43 .
[3] WANG Fu-Qing LI Min QU Yong-Mei. Observation on Microstructure of Male Abortion in Chinese Cabbage[J]. Chin Bull Bot, 2001, 18(01): 105 -109 .
[4] Wu Xian-jun;Li Ping;Zhao Zhen-ju;Wang Qian;Li Chao-luan;Huang Rong and Cheng Fa-ling. Studies on the biological characteristics of Cycas panzhihuaensis, I. Morphology and anatomy of vegetative organs[J]. Chin Bull Bot, 1995, 12(专辑): 38 -40 .
[5] Bin Jin-hua and Pan Rui-zhi. Methyl Jasmonates: Biochemistry Biophysiolgy and Role in Plant Resistance[J]. Chin Bull Bot, 1995, 12(04): 17 -21 .
[6] Junbin Zhao;;Yiping Zhang;;Fuqiang Song;Zaifu Xu;Laiyun Xiao. Spring Phenology of Introduced Species in Response to Extreme Chilliness in Xishuangbanna Tropical Botanical Garden[J]. Chin Bull Bot, 2010, 45(04): 435 -443 .
[7] Yin Hong-zhang(H. C. Yin) and Xia zhen-au(Hsia Chen-au). The Fifty Years of Plant Physiology in China[J]. Chin Bull Bot, 1983, 1(02): 1 -6 .
[8] Chen Chun-xian;Sun Jing-san and Zhu Li-huang. Genetic Basis on Albinos Frequently Derived from Anther Culture[J]. Chin Bull Bot, 1997, 14(04): 13 -17 .
[9] Xing Jian-min;Zha Li-hang;Li Zuo-hu;Liu Da-lu;Ye He-chun and Li Guo-feng. Advances in the Study on Taxol Production by Plant Cell Culture[J]. Chin Bull Bot, 1997, 14(03): 22 -29 .
[10] Zhang Zhong-ming;Cui Ke-ming and Fan Yong-jun. Staining Plant Material Section With Toluiding Blue O Before Removal of Paraffin[J]. Chin Bull Bot, 1997, 14(02): 58 -60 .