Plant Diversity ›› 2023, Vol. 45 ›› Issue (04): 456-468.DOI: 10.1016/j.pld.2022.10.001
• Articles • Previous Articles Next Articles
Ting-Ting Zou, Sen-Tao Lyu, Qi-Lin Jiang, Shu-He Shang, Xiao-Fan Wang
Received:
2022-06-07
Revised:
2022-10-04
Online:
2023-08-21
Published:
2023-07-25
Contact:
Xiao-Fan Wang,E-mail:wangxf@whu.edu.cn
Supported by:
Ting-Ting Zou, Sen-Tao Lyu, Qi-Lin Jiang, Shu-He Shang, Xiao-Fan Wang
通讯作者:
Xiao-Fan Wang,E-mail:wangxf@whu.edu.cn
基金资助:
Ting-Ting Zou, Sen-Tao Lyu, Qi-Lin Jiang, Shu-He Shang, Xiao-Fan Wang. Pre- and post-pollination barriers between two exotic and five native Sagittaria species: Implications for species conservation[J]. Plant Diversity, 2023, 45(04): 456-468.
Ting-Ting Zou, Sen-Tao Lyu, Qi-Lin Jiang, Shu-He Shang, Xiao-Fan Wang. Pre- and post-pollination barriers between two exotic and five native Sagittaria species: Implications for species conservation[J]. Plant Diversity, 2023, 45(04): 456-468.
[1] Adair, R., Keener, B., Kwong, R., et al., 2012. The biology of Australian weeds 58. Sagittaria platyphylla (Engelmann) J.G.Smith, S. montevidensis Cham. & Schltdl. and S. calycina Engelmann. Plant Protect. Q. 27, 47-58. [2] Ainouche, M.L., Fortune, P.M., Salmon, A., et al., 1999. Hybridization, polyploidy and invasion: lessons from Spartina (Poaceae). Biol. Invasions 11, 1159-1173. [3] Archibald, J.K., Mort, M.E., Crawford, D.J., et al., 2005. Life history affects the evolution of reproductive isolation among species of Coreopsis (Asteraceae). Evolution 59, 2362-2369. [4] Ayres, D.R., Garcia-Rossi, D., Davis, H.G., et al., 1999. Extent and degree of hybridization between exotic (Spartina alterniflora) and native (S. foliosa) cordgrass (Poaceae) in California, USA determined by random amplified polymorphic DNA (RAPDs). Mol. Ecol. 8, 1179-1186. [5] Baack, E., Melo, M.C., Rieseberg, L.H., et al., 2015. The origins of reproductive isolation in plants. New Phytol. 207, 968-984. [6] Baldwin, B.G., 1992. Phylogenetic utility of the internal transcribed spacers of nuclear ribosomal DNA in plants: an example from the Compositae. Mol. Phylogenet. Evol. 1, 3-16. [7] Bandelt, H-J., Forster, P., Rohl, A., 1999. Median-joining networks for inferring intraspecific phylogenies. Mol. Biol. Evol. 16, 37-48. [8] Beans, C.M., Roach, D.A., 2015. An invasive plant alters pollinator-mediated phenotypic selection on a native congener. Am. J. Bot. 102, 50-57. [9] Bertin, R.I., 1990. Paternal success following mixed pollinations of Campsis radicans. Am. Midl. Nat. 124, 153-163. [10] Brock, M.T., 2009. Prezygotic barriers to gene flow between Taraxacum ceratophorum and the invasive Taraxacum officinale (Asteraceae). Oecologia 161, 241-251. [11] Brys, R., Broeck, A.V., Mergeay, J., et al., 2014. The contribution of mating system variation to reproductive isolation in two closely related Centaurium species (Gentianaceae) with a generalized flower morphology. Evolution 68, 1281-1293. [12] Brys, R., van Cauwenberghe, J., Jacquemyn, H., et al., 2016. The importance of autonomous selfing in preventing hybridization in three closely related plant species. J. Ecol. 104, 601-610. [13] Burgess, K.S., Morgan, M., Husband, B.C., 2008. Interspecific seed discounting and the fertility cost of hybridization in an endangered species. New Phytol. 177, 276-284. [14] Carney, S.E., Hodges, S.A., Arnold, M.L., 1996. Effects of differential pollen-tube growth on hybridization in the Louisiana irises. Evolution 50, 1871-1878. [15] Castro, M., Loureiro, J., Husband, B.C., et al., 2020. The role of multiple reproductive barriers: strong post-pollination interactions govern cytotype isolation in a tetraploid-octoploid contact zone. Ann. Bot. 126, 991-1003. [16] Chen, J-K., 1989. Systematic and Evolutionary Botanical Studies on Chinese Sagittaria. Wuhan University Press, Wuhan. [17] Coyne, J.A., Orr, H.A., 1989. Patterns of speciation in Drosophila. Evolution 43, 362-381. [18] Coyne, J.A., Orr, H.A., 1997. “Patterns of speciation in Drosophila” revisited. Evolution 51, 295-303. [19] Dell'olivo, A., Hoballah, M.E., Gubitz, T., et al., 2011. Isolation barriers between Petunia axillaris and Petunia integrifolia (Solanaceae). Evolution 65, 1979-1991. [20] Diaz, A., Macnair, M.R., 1999. Pollen tube competition as a mechanism of prezygotic reproductive isolation between Mimulus nasutus and its presumed progenitor M. guttatus. New Phytol. 144, 471-478. [21] Dietzsch, A.C., Stanley, D.A., Stout, J.C., 2011. Relative abundance of an invasive alien plant affects native pollination processes. Oecologia 167, 469-479. [22] Ellstrand, N.C., Schierenbeck, K.A., 2006. Hybridization as a stimulus for the evolution of invasiveness in plants? Euphytica 148, 35-46. [23] Huang, S-Q., 2003. Flower dimorphism and the maintenance of andromonoecy in Sagittaria guyanensis ssp. lappula (Alismataceae). New Phytol. 157, 357-364. [24] Huang, S-Q., Shi, X-Q., 2013. Floral isolation in Pedicularis: how do congeners with shared pollinators minimize reproductive interference? New Phytol. 199, 858-865. [25] Huang, S-Q., Song, N., Wang, Q., et al., 2000. Sex expression and the evolutionary advantages of male flowers in an andromonoecious species, Sagittaria guyanensis subsp. lappula (Alismataceae). Acta Bot. Sin. 42, 1108-1114. [26] Huang, S-Q., Tang, L-L., Sun, J-F., et al., 2006. Pollinator response to female and male floral display in a monoecious species and its implications for the evolution of floral dimorphism. New Phytol. 171, 417-424. [27] Jewell, C., Papineau, A.D., Freyre, R., et al., 2012. Patterns of reproductive isolation in Nolana (Chilean bellflower). Evolution 66, 2628-2636. [28] Keller, B., Ganz, R., Mora-Carrera, E., et al., 2021. Asymmetries of reproductive isolation are reflected in directionalities of hybridization: integrative evidence on the complexity of species boundaries. New Phytol. 229, 1795-1809. [29] Kellner, A., Ritz, C.M., Wissemann, V., 2012. Hybridization with invasive Rosa rugosa threatens the genetic integrity of native Rosa mollis. Bot. J. Linn. Soc. 170, 472-484. [30] Knope, M.L., Pender, R.J., Crawford, D.J., et al., 2013. Invasive congeners are unlikely to hybridize with native Hawaiian Bidens (Asteraceae). Am. J. Bot. 100, 1221-1226. [31] Larcombe, M.J., Silva, J.C., Tilyard, P., et al., 2016. On the persistence of reproductive barriers in Eucalyptus: the bridging of mechanical barriers to zygote formation by F1 hybrids is counteracted by intrinsic post-zygotic incompatibilities. Ann. Bot. 118, 431-444. [32] Levin, D.A., Francisco-Ortega, J., Jansen, R.K., 1996. Hybridization and the extinction of rare plant species. Conserv. Biol. 10, 10-16. [33] Librado, P., Rozas, J., 2009. DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics 25, 1451-1452. [34] Lowry, D.B., Modliszewski, J.L., Wright, K.M., et al., 2008. The strength and genetic basis of reproductive isolating barriers in flowering plants. Philos. Trans. R. Soc. B-Biol. Sci. 363, 3009-3021. [35] Lyu, N., Du, W., Wang, X-F., 2016. Unique growth paths of heterospecific pollen tubes result in late entry into ovules in the gynoecium of Sagittaria (Alismataceae). Plant Biol. 19, 108-114. [36] Ma, Y-P., Xie, W-J., Sun, W-B., et al., 2016. Strong reproductive isolation despite occasional hybridization between a widely distributed and a narrow endemic Rhododendron species. Sci. Rep. 6, 19146. [37] Ma, Y.P., Marczewski, T., Xue, D., et al., 2019. Conservation implications of asymmetric introgression and reproductive barriers in a rare primrose species. BMC Plant Biol. 19, 286. [38] Mack, R.N., Simberloff, D., Mark Lonsdale, W., et al., 2000. Biotic Invasions: causes, epidemiology, global consequences, and control. Ecol. Appl. 10, 689-710. [39] Martin, F.D., 1970. Pollen germination on foreign stigmas. Bull. Torrey Bot. Club 97, 1-6. [40] Matallana, G., Oliveira, P.E., da Silva, P.R.R., et al., 2016. Post-pollination barriers in an assemblage of Bromeliaceae in south-eastern Brazil. Bot. J. Linn. Soc. 181, 521-531. [41] Matsumoto, T.K., Hirobe, M., Sueyoshi, M., et al., 2021. Selective pollination by fungus gnats potentially functions as an alternative reproductive isolation among five Arisaema species. Ann. Bot. 127, 633-644. [42] McFarlane, S.E., Pemberton, J.M., 2019. Detecting the true extent of introgression during anthropogenic hybridization. Trends Ecol. Evol. 34, 315-326. [43] Miguez, M.B., Amela Garcia, M.T., 2019. Breeding system, floral biology and pollinators of Sagittaria montevidensis subsp. montevidensis Cham. et Schlech. (Alismataceae). Aquat. Bot. 158. [44] Minnaar, C., de Jager, M.L., Anderson, B., 2019. Intraspecific divergence in floral-tube length promotes asymmetric pollen movement and reproductive isolation. New Phytol. 224, 1160-1170. [45] Montgomery, B.R., Soper, D.M., Delph, L.F., 2010. Asymmetrical conspecific seed-siring advantage between Silene latifolia and S. dioica. Ann. Bot. 105, 595-605. [46] Morales, C.L., Traveset, A., 2008. Interspecific pollen transfer: magnitude, prevalence and consequences for plant Fitness. Crit. Rev. Plant Sci. 27, 221-238. [47] Moreira-Hernandez, J.I., Muchhala, N., 2019. Importance of pollinator-mediated interspecific pollen transfer for angiosperm evolution. Annu. Rev. Ecol. Evol. Syst. 50, 191-217. [48] Munguia-Rosas, M.A., Jacome-Flores, M.E., 2020. Reproductive isolation between wild and domesticated chaya (Cnidoscolus aconitifolius) in sympatry. Plant Biol. 22, 932-938. [49] Ndlovu, M.S., Coetzee, J.A., Nxumalo, M.M., et al., 2020. The establishment and rapid spread of Sagittaria platyphylla in South Africa. Water 12, 1472. [50] Nishida, S., Kanaoka, M.M., Hashimoto, K., et al., 2014. Pollen-pistil interactions in reproductive interference: comparisons of heterospecific pollen tube growth from alien species between two native Taraxacum species. Funct. Ecol. 28, 450-457. [51] Owens, G.L., Rieseberg, L.H., 2014. Hybrid incompatibility is acquired faster in annual than in perennial species of sunflower and tarweed. Evolution 68, 893-900. [52] Paudel, B.R., Burd, M., Shrestha, M. et al., 2018. Reproductive isolation in alpine gingers: how do coexisting Roscoea (R. purpurea and R. tumjensis) conserve species integrity? Evolution 72, 1840-1850. [53] Qiu, J., Gao, C., Wei, H.L., et al., 2021. Flowering biology of Rhododendron pulchrum. Horticulturae 7, 508. [54] Ramsey, J., Bradshaw, H.D., Schemske, D.W., 2003. Components of reproductive isolation between the monkeyflowers Mimulus lewisii and M. cardinalis (Phrymaceae). Evolution 57, 1520-1534. [55] Rozas, J., Ferrer-Mata, A., Sanchez-DelBarrio, J.C., et al., 2017. DnaSP 6: DNA sequence polymorphism analysis of large data sets. Mol. Biol. Evol. 34, 3299-3302. [56] Sanchez-Vilas, J., Turner, A., Pannell, J.R., 2011. Sexual dimorphism in intra- and interspecific competitive ability of the dioecious herb Mercurialis annua. Plant Biol. 13, 218-222. [57] Sobel, J.M., Chen, G.F., 2014. Unification of methods for estimating the strength of reproductive isolation. Evolution 68, 1511-1522. [58] Tamura, K., Stecher, G., Kumar, S., 2021. MEGA11: molecular evolutionary genetics analysis version 11. Mol. Biol. Evol. 38, 3022-3027. [59] Tang, J., Sun, S-G., Haung, S-Q., 2022. Experimental sympatry suggests geographic isolation as an essential reproductive barrier between two sister species of Pedicularis. J. Systemat. Evol. 00, 1-12. [60] Todesco, M., Pascual, M.A., Owens, G.L., et al., 2016. Hybridization and extinction. Evol. Appl. 9, 892-908. [61] Tong, Z-Y., Huang, S-Q., 2016. Pre- and post-pollination interaction between six co-flowering Pedicularis species via heterospecific pollen transfer. New Phytol. 211, 1452-1461. [62] Walsh, P.S., Metzger, D.A., Higushi, R., 1991. Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material. Biotechniques 10, 506-513. [63] Wang, H., Wang, Q., Bowler, P., et al., 2016. Invasive aquatic plants in China. Aquat. Invasions 11, 1-9. [64] Wang, H., Xiao, K.Y., Wu, Z.G., et al., 2020. Delta arrowhead (Sagittaria platyphylla) in the Yangtze River: an invasive aquatic plant and the potential ecological consequences. BioInvasions Rec. 9, 618-626. [65] Wang, Q.F., Li, W., Wang, G.X., et al., 2021. Aquatic Plant of China. Hubei Science and Technology Press. Wuhan. [66] Wang, X-F., Tan, Y-Y., Chen, J-H., et al., 2006. Pollen tube reallocation in two preanthesis cleistogamous species, Ranalisma rostratum and Sagittaria guyanensis ssp. lappula (Alismataceae). Aquat. Bot. 85, 233-240. [67] Zaya, D.N., Leicht-Young, S.A., Pavlovic, N.B., et al., 2015. Genetic characterization of hybridization between native and invasive bittersweet vines (Celastrus spp.). Biol. Invasions 17, 2975-2988. [68] Zhang, Z.H., Rengel, Z., Meney, K., 2007. Growth and resource allocation of Canna indica and Schoenoplectus validus as affected by interspecific competition and nutrient availability. Hydrobiologia 589, 235-248. [69] Zhong, S., Liu, M.L., Wang, Z.J., et al., 2019. Cysteine-rich peptides promote interspecific genetic isolation in Arabidopsis. Science 364, 851. [70] Zou, T-T., 2022. ITS sequence of native and alien Sagittaria species and their hybrids. Figshare. Dataset. [71] Zou, T-T., Wang, C-H., Lyu, S.-T., et al., 2022. Effects of heterospecific pollen on stigma behavior in Campsis radicans: causes and consequences. Am. J. Bot. 109, 1-12. |
[1] | Fei-Fei Li, Qiang Hao, Xia Cui, Ruo-Zhu Lin, Bin-Sheng Luo, Jin-Shuang Ma. Global invasive alien plant management lists: Assessing current practices and adapting to new demands [J]. Plant Diversity, 2025, 47(04): 666-680. |
[2] | Zhi-Li Zhou (周知里), Tial C. Ling, Jian-Li Zhao (赵建立), Xin-Zhi Wang (王欣之), Lin-Lin Wang (王林林), Li Li (李莉), Wen-Jing Wang (王雯婧), Dong-Rui Jia (贾东瑞), Zhi-Kun Wu (吴之坤), Xu-Dong Sun (孙旭东), Yong-Ping Yang (杨永平), Yuan-Wen Duan (段元文). Parallel loss of anthocyanins triggers the incipient sympatric speciation in an alpine ginger [J]. Plant Diversity, 2025, 47(03): 429-439. |
[3] | Wei Gu, Ting Zhang, Shui-Yin Liu, Qin Tian, Chen-Xuan Yang, Qing Lu, Xiao-Gang Fu, Heather R. Kates, Gregory W. Stull, Pamela S. Soltis, Douglas E. Soltis, Ryan A. Folk, Robert P. Guralnick, De-Zhu Li, Ting-Shuang Yi. Phylogenomics, reticulation, and biogeographical history of Elaeagnaceae [J]. Plant Diversity, 2024, 46(06): 683-697. |
[4] | Sen-Tao Lyu, Ting-Ting Zou, Qi-Lin Jiang, Xiao-Fan Wang. Maintenance of andromonoecy in an autogamous species: Superior male function in male flowers of the endangered Sagittaria guayanensis [J]. Plant Diversity, 2024, 46(06): 783-790. |
[5] | Yiqing Chen, Lina Dong, Huiqin Yi, Catherine Kidner, Ming Kang. Genomic divergence and mutation load in the Begonia masoniana complex from limestone karsts [J]. Plant Diversity, 2024, 46(05): 575-584. |
[6] | Liping Shan, Meng Hou. Herbivore and native plant diversity synergistically resist alien plant invasion regardless of nutrient conditions [J]. Plant Diversity, 2024, 46(05): 640-647. |
[7] | Hui Feng, Achyut Kumar Banerjee, Wuxia Guo, Yang Yuan, Fuyuan Duan, Wei Lun Ng, Xuming Zhao, Yuting Liu, Chunmei Li, Ying Liu, Linfeng Li, Yelin Huang. Origin and evolution of a new tetraploid mangrove species in an intertidal zone [J]. Plant Diversity, 2024, 46(04): 476-490. |
[8] | Zhen Yang, Lisong Liang, Weibo Xiang, Lujun Wang, Qinghua Ma, Zhaoshan Wang. Conservation genomics provides insights into genetic resilience and adaptation of the endangered Chinese hazelnut, Corylus chinensis [J]. Plant Diversity, 2024, 46(03): 294-308. |
[9] | Xiang-Zhou Hu, Cen Guo, Sheng-Yuan Qin, De-Zhu Li, Zhen-Hua Guo. Deep genome skimming reveals the hybrid origin of Pseudosasa gracilis (Poaceae: Bambusoideae) [J]. Plant Diversity, 2024, 46(03): 344-352. |
[10] | Yumeng Ren, Lushui Zhang, Xuchen Yang, Hao Lin, Yupeng Sang, Landi Feng, Jianquan Liu, Minghui Kang. Cryptic divergences and repeated hybridizations within the endangered “living fossil” dove tree (Davidia involucrata) revealed by whole genome resequencing [J]. Plant Diversity, 2024, 46(02): 169-180. |
[11] | Jian-Feng Huang, Clive T. Darwell, Yan-Qiong Peng. Enhanced and asymmetric signatures of hybridization at climatic margins: Evidence from closely related dioecious fig species [J]. Plant Diversity, 2024, 46(02): 181-193. |
[12] | Yu-Juan Zhao, Gen-Shen Yin, Xun Gong. RAD-sequencing improves the genetic characterization of a threatened tree peony (Paeonia ludlowii) endemic to China: Implications for conservation [J]. Plant Diversity, 2023, 45(05): 513-522. |
[13] | Dan-Qi Li, Lu Jiang, Hua Liang, Da-Hai Zhu, Deng-Mei Fan, Yi-Xuan Kou, Yi Yang, Zhi-Yong Zhang. Resolving a nearly 90-year-old enigma: The rare Fagus chienii is conspecific with F. hayatae based on molecular and morphological evidence [J]. Plant Diversity, 2023, 45(05): 544-551. |
[14] | Lin Lin, Xiao-Long Jiang, Kai-Qi Guo, Amy Byrne, Min Deng. Climate change impacts the distribution of Quercus section Cyclobalanopsis (Fagaceae), a keystone lineage in East Asian evergreen broadleaved forests [J]. Plant Diversity, 2023, 45(05): 552-568. |
[15] | Hong Qian. Intercontinental comparison of phylogenetic relatedness in introduced plants at the transition from naturalization to invasion: A case study on the floras of South Africa and China [J]. Plant Diversity, 2023, 45(04): 363-368. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||