Chinese Bulletin of Botany ›› 2023, Vol. 58 ›› Issue (5): 733-742.DOI: 10.11983/CBB22225
• EXPERIMENTAL COMMUNICATIONS • Previous Articles Next Articles
Ren Dengfu1, Zhai Yaxin2, Zhang Aiqin1,*()
Received:
2022-09-21
Accepted:
2023-02-28
Online:
2023-09-01
Published:
2023-09-21
Contact:
*E-mail: 1131646332@qq.com
Ren Dengfu, Zhai Yaxin, Zhang Aiqin. The Variation of Reciprocal Herkogamy in Five Distylous Populations of Goniolimon speciosum in Xinjiang[J]. Chinese Bulletin of Botany, 2023, 58(5): 733-742.
Figure 1 The flowering branch, floral morphs, pollen and stigma morphology in Goniolimon speciosum (A) Flowering branch; (B), (C) Flowers with S- and L-morph; (D) Pistil and stamen of H-morph; (E), (H) Pollen and stigma morphology of L-morph; (F), (I) Pollen and stigma morphology of S- and HS-morph; (G), (J) Pollen and stigma morphology of HL-morph. S-morph: Flower with stigma significantly lower than the anther, as short-styled morph flower; L-morph: Flower with stigma significantly higher than the anther, as long-styled morph flower; H-morph: Flower with stigma and anther in the same position, as homostylous morph flower; HS-morph: Flower with the same pollen and stigma morphology as S-morph flower; HL-morph: Flower with the same pollen and stigma morphology as L-morph flower. (A) Bar=2 cm; (B)-(D) Bars=2 mm; (E)-(G) Bars=10 μm; (H)-(J) Bars=20 μm
Population | Location | Number of plant samples (L, S, H) | Floral morph frequency (L/S/H) | Proportion of H-morph (%) | χ2 (L/S) | P-values (L/S) |
---|---|---|---|---|---|---|
KNS | 87.024°E, 48.698°N, 1424 m | 166, 212, 91 | 1.82/2.33/1 | 32.62 | 5.598 | 0.018 |
HXG | 87.984°E, 43.811°N, 1853 m | 104, 162, 105 | 0.99/1.54/1 | 28.30 | 12.674 | 0.000 |
NS | 87.233°E, 43.517°N, 1904 m | 82, 113, 44 | 1.86/2.57/1 | 18.41 | 4.928 | 0.026 |
GG | 87.167°E, 43.500°N, 1919 m | 44, 51, 34 | 1.29/1.50/1 | 26.36 | 0.516 | 0.473 |
ZS | 80.988°E, 43.150°N, 1980 m | 52, 68, 40 | 1.30/1.70/1 | 25.00 | 2.133 | 0.144 |
Table 1 The floral morph composition and frequency in five populations of Goniolimon speciosum
Population | Location | Number of plant samples (L, S, H) | Floral morph frequency (L/S/H) | Proportion of H-morph (%) | χ2 (L/S) | P-values (L/S) |
---|---|---|---|---|---|---|
KNS | 87.024°E, 48.698°N, 1424 m | 166, 212, 91 | 1.82/2.33/1 | 32.62 | 5.598 | 0.018 |
HXG | 87.984°E, 43.811°N, 1853 m | 104, 162, 105 | 0.99/1.54/1 | 28.30 | 12.674 | 0.000 |
NS | 87.233°E, 43.517°N, 1904 m | 82, 113, 44 | 1.86/2.57/1 | 18.41 | 4.928 | 0.026 |
GG | 87.167°E, 43.500°N, 1919 m | 44, 51, 34 | 1.29/1.50/1 | 26.36 | 0.516 | 0.473 |
ZS | 80.988°E, 43.150°N, 1980 m | 52, 68, 40 | 1.30/1.70/1 | 25.00 | 2.133 | 0.144 |
Floral parameter | Population | S-morph (n=20-30) | L-morph (n=20-30) | H-morph (n=20-30) |
---|---|---|---|---|
Corolla tube length (mm) | KNS | (6.20±0.10)a | (6.03±0.11)a | (6.17±0.11)a |
Corolla opening diameter (mm) | KNS | (6.17±0.09)a | (6.02±0.14)a | (6.09±0.13)a |
Pistil height (mm) | KNS | (6.93±0.09)c | (8.39±0.09)a | (7.84±0.11)b |
Stamen height (mm) | KNS | (8.26±0.06)a | (7.13±0.06)c | (7.81±0.07)b |
Number of pollen grains per flower | KNS | (1127±46)a | (1158±36)a | (1110±24)a |
Number of ovules per flower | KNS | 1 | 1 | 1 |
Number of stigmatic pollen loads (total, inter-morph) | KNS | (17±3)b, (2.5±0.7)a | (27±4)ab, (1.4±0.4)a | (33±7)a, (1.3±0.5)a |
GG | (25±3)b, (0.6±0.3)a | (49±3)a, (1.1±0.3)a | (56±13)a, (1.6±0.9)a | |
ZS | (22±3)b, (0.7±0.3)a | (54±4)a, (1.1±0.3)a | (54±5)a, (1.1±0.3)a |
Table 2 Comparisons of floral parameters of Kanasi (KNS) population and stigmatic pollen loads among floral morphs in three field populations in Goniolimon speciosum
Floral parameter | Population | S-morph (n=20-30) | L-morph (n=20-30) | H-morph (n=20-30) |
---|---|---|---|---|
Corolla tube length (mm) | KNS | (6.20±0.10)a | (6.03±0.11)a | (6.17±0.11)a |
Corolla opening diameter (mm) | KNS | (6.17±0.09)a | (6.02±0.14)a | (6.09±0.13)a |
Pistil height (mm) | KNS | (6.93±0.09)c | (8.39±0.09)a | (7.84±0.11)b |
Stamen height (mm) | KNS | (8.26±0.06)a | (7.13±0.06)c | (7.81±0.07)b |
Number of pollen grains per flower | KNS | (1127±46)a | (1158±36)a | (1110±24)a |
Number of ovules per flower | KNS | 1 | 1 | 1 |
Number of stigmatic pollen loads (total, inter-morph) | KNS | (17±3)b, (2.5±0.7)a | (27±4)ab, (1.4±0.4)a | (33±7)a, (1.3±0.5)a |
GG | (25±3)b, (0.6±0.3)a | (49±3)a, (1.1±0.3)a | (56±13)a, (1.6±0.9)a | |
ZS | (22±3)b, (0.7±0.3)a | (54±4)a, (1.1±0.3)a | (54±5)a, (1.1±0.3)a |
Figure 3 Comparisons of fruit set of floral morphs under four pollination treatments in Goniolimon speciosum Different lowercase letters indicate significant differences among treatments (P<0.05).
[1] | 阿依古丽·阿卜杜热伊木, 焦芳芳, 张爱勤, (2021). 异型花柱植物喀什补血草的传粉者功能群与花粉转移效率. 植物生态学报 45, 51-61. |
[2] |
周伟, 王红 (2009). 被子植物异型花柱及其进化意义. 植物学报 44, 742-751.
DOI |
[3] |
Armbruster WS, Pérez-Barrales R, Arroyo J, Edwards ME, Vargas P (2006). Three-dimensional reciprocity of floral morphs in wild flax (Linum suffruticosum): a new twist on heterostyly. New Phytol 171, 581-590.
PMID |
[4] |
Baker HG (1948). Dimorphism and monomorphism in the Plumbaginaceae. I. Aurvey of the family. Ann Bot 12, 207-219.
DOI URL |
[5] |
Baker HG (1966). The evolution, functioning and breakdown of heteromorphic incompatibility systems. I. The Plumbaginaceae. Evolution 20, 349-368.
DOI PMID |
[6] | Barrett SCH (1992). Heterostylous genetic polymorphisms:model systems for evolutionary analysis. In: Barrett SCH, ed. Evolution and Function of Heterostyly. Berlin: Springer-Verlag. pp. 1-29. |
[7] |
Barrett SCH (2002). Sexual interference of the floral kind. Heredity 88, 154-159.
PMID |
[8] |
Barrett SCH (2019). ‘A most complex marriage arrangement’: recent advances on heterostyly and unresolved questions. New Phytol 224, 1051-1067.
DOI URL |
[9] |
Brys R, Jacquemyn H (2020). The impact of individual inaccuracy of reciprocal herkogamy on legitimate pollen deposition and seed set in a distylous self-incompatible herb. J Ecol 108, 81-93.
DOI URL |
[10] |
Brys R, Jacquemyn H, Beeckman T (2008). Morph-ratio variation, population size and female reproductive success in distylous Pulmonaria officinalis (Boraginaceae). J Evol Biol 21, 1281-1289.
DOI URL |
[11] |
Charlesworth D, Charlesworth B (1979). A model for the evolution of distyly. Am Nat 114, 467-498.
DOI URL |
[12] |
Chen ML (2012). Floral morphology and breeding system in Polygonum hastato-sagittatum Mak. (Polygonaceae). Flora 207, 365-371.
DOI URL |
[13] |
Costa J, Castro S, Loureiro J, Barrett SCH (2017). Experimental insights on the function of ancillary pollen and stigma polymorphisms in plants with heteromorphic incompatibility. Evolution 71, 121-134.
DOI PMID |
[14] | Darwin CR (1877). The different forms of flowers on plants of the same species. London: John Murray. pp. 244-277. |
[15] | Dulberger R (1975). Intermorph structural differences between stigmatic papillae and pollen grains in relation to incompatibility in Plumbaginaceae. Proc Roy Soc B Biol Sci 188, 257-274. |
[16] | Dulberger R (1992). Floral polymorphisms and their functional significance in the heterostylous syndrome. In: Barrett SCH, ed. Evolution and Function of Heterostyly. Berlin: Springer-Verlag. pp. 41-84. |
[17] |
Ferrero V, Castro S, Sánchez JM, Navarro L (2011). Stigma-anther reciprocity, pollinators, and pollen transfer efficiency in populations of heterostylous species of Lithodora and Glandora (Boraginaceae). Plant Syst Evol 291, 267-276.
DOI URL |
[18] |
Fisher RA (1935). On the selective consequences of East’s (1927) theory of heterostylism in Lythrum. J Genet 30, 369-382.
DOI URL |
[19] |
Ganders FR (1979). The biology of heterostyly. New Zeal J Bot 17, 607-635.
DOI URL |
[20] |
Haddadchi A, Fatemi M (2015). Self-compatibility and floral traits adapted for self-pollination allow homostylous Nymphoides geminata (Menyanthaceae) to persist in marginal habitats. Plant Syst Evol 301, 239-250.
DOI URL |
[21] | Huu CN, Plaschil S, Himmelbach A, Kappel C, Lenhard M (2022). Female self-incompatibility type in heterostylous Primula is determined by the brassinosteroid-inactivating cytochrome P450 CYP734A50. Curr Biol 32, 671-676. |
[22] | Jiang XF, Zhu XF, Li QJ (2018). Variation in the degree of reciprocal herkogamy affects the degree of legitimate pollination in a distylous species. AoB Plants 10, ply022. |
[23] |
Kéry M, Matthies D, Schmid B (2003). Demographic stochasticity in population fragments of the declining distylous perennial Primula veris (Primulaceae). Basic Appl Ecol 4, 197-206.
DOI URL |
[24] | Kubitzki K (1993). Plumbaginaceae. In: Kubitzki K, Rohwer JG, Bittrich V, eds. Flowering Plants. Dicotyledons: Magnoliid, Hamamelid and Caryophyllid Families. Berlin: Springer- Verlag. pp. 523-530. |
[25] |
Liu SJ, Wu LY, Huang SQ (2016). Shortened anther-stigma distance reduces compatible pollination in two distylous Primula species. J Plant Ecol 9, 224-232.
DOI URL |
[26] |
Lloyd DG, Webb CJ (1986). The avoidance of interference between the presentation of pollen and stigmas in angiosperms I. Dichogamy. New Zeal J Bot 24, 135-162.
DOI URL |
[27] | Lloyd DG, Webb CJ (1992). The selection of heterostyly. In: Barrett SCH, ed. Evolution and Function of Heterostyly. Berlin: Springer-Verlag. pp. 179-207. |
[28] |
Mather K, de Winton D (1941). Adaptation and counter- adaptation of the breeding system in Primula: the nature of breeding systems. Ann Bot 5, 297-311.
DOI URL |
[29] |
Matias R, Pérez-Barrales R, Consolaro H (2020). Patterns of variation in distylous traits and reproductive consequences in Erythroxylum species and populations. Am J Bot 107, 910-922.
DOI URL |
[30] |
Matzke CM, Hamam HJ, Henning PM, Dougherty K, Shore JS, Neff MM, McCubbin AG (2021). Pistil mating type and morphology are mediated by the brassinosteroid inactivating activity of the S-locus gene BAHD in heterostylous Turnera species. Int J Mol Sci 22, 10603.
DOI URL |
[31] |
Mora-Carrera E, Stubbs RL, Keller B, Léveillé-Bourret É, de Vos JM, Szövényi P, Conti E (2023). Different molecular changes underlie the same phenotypic transition: origins and consequences of independent shifts to homostyly within species. Mol Ecol 32, 61-78.
DOI URL |
[32] |
Pérez-Barrales R, Arroyo J (2010). Pollinator shifts and the loss of style polymorphism in Narcissus papyraceus (Amaryllidaceae). J Evol Biol 23, 1117-1128.
DOI URL |
[33] |
Pérez-Barrales R, Arroyo J, Armbruster WS (2007). Differences in pollinator faunas may generate geographic differences in floral morphology and integration in Narcissus papyraceus (Amaryllidaceae). Oikos 116, 1904-1918.
DOI URL |
[34] |
Santos-Gally R, de Castro A, Pérez-Barrales R, Arroyo J (2015). Stylar polymorphism on the edge: unusual flower traits in Moroccan Narcissus broussonetii (Amaryllidaceae). Bot J Linn Soc 177, 644-656.
DOI URL |
[35] |
Shibayama Y, Kadono Y (2003). Floral morph composition and pollen limitation in the seed set of Nymphoides indica populations. Ecol Res 18, 725-737.
DOI URL |
[36] |
Simón-Porcar VI, Santos-Gally R, Arroyo J (2014). Long- tongued insects promote disassortative pollen transfer in style-dimorphic Narcissus papyraceus (Amaryllidaceae). J Ecol 102, 116-125.
DOI URL |
[37] |
Takeshima R, Nishio T, Komatsu S, Kurauchi N, Matsui K (2019). Identification of a gene encoding polygalacturonase expressed specifically in short styles in distylous common buckwheat (Fagopyrum esculentum). Heredity 123, 492-502.
DOI PMID |
[38] |
Tamari F, Shore JS (2004). Distribution of style and pollen polygalacturonases among distylous and homostylous Turnera and Piriqueta spp. (Turneraceae). Heredity 92, 380-385.
PMID |
[39] | Washitani I (2000). Creeping ‘fruitless falls’:reproductive failure in heterostylous plants in fragmented landscapes. In: Kato M, ed. The Biology of Biodiversity. Tokyo: Tokyo: Springer-Verlag. pp. 133-145. |
[40] |
Wu LY, Chang FF, Liu SJ, Armbruster WS, Huang SQ (2018). Heterostyly promotes compatible pollination in buckwheats: comparisons of intraflower, intraplant, and interplant pollen flow in distylous and homostylous Fagopyrum. Am J Bot 105, 108-116.
DOI URL |
[41] |
Yuan S, Barrett SCH, Duan TT, Qian X, Shi MM, Zhang DX (2017). Ecological correlates and genetic consequences of evolutionary transitions from distyly to homostyly. Ann Bot 120, 775-789.
DOI URL |
[42] |
Yuan S, Barrett SCH, Li CH, Li XJ, Xie KP, Zhang DX (2019). Genetics of distyly and homostyly in a self-compatible Primula. Heredity 122, 110-119.
DOI |
[43] |
Zhang W, Hu YF, He X, Zhou W, Shao JW (2021). Evolution of autonomous selfing in marginal habitats: spatiotemporal variation in the floral traits of the distylous Primula wannanensis. Front Plant Sci 12, 781281.
DOI URL |
[44] |
Zhong L, Barrett SCH, Wang XJ, Wu ZK, Sun HY, Li DZ, Wang H, Zhou W (2019). Phylogenomic analysis reveals multiple evolutionary origins of selfing from outcrossing in a lineage of heterostylous plants. New Phytol 224, 1290-1303.
DOI PMID |
[45] |
Zhou W, Barrett SCH, Li HD, Wu ZK, Wang XJ, Wang H, Li DZ (2017). Phylogeographic insights on the evolutionary breakdown of heterostyly. New Phytol 214, 1368-1380.
DOI PMID |
[46] |
Zhou W, Barrett SCH, Wang H, Li DZ (2015). Reciprocal herkogamy promotes disassortative mating in a distylous species with intramorph compatibility. New Phytol 206, 1503-1512.
DOI PMID |
[47] |
Zhu XF, Jiang XF, Li L, Zhang ZQ, Li QJ (2015). Asymmetrical disassortative pollination in a distylous primrose: the complementary roles of bumblebee nectar robbers and syrphid flies. Sci Rep 5, 7721.
DOI |
[1] | Ayiguli ABUDUREYIMU, JIAO Fang-Fang, ZHANG Ai-Qin. Pollinator functional groups and their pollen transfer efficiency in heterostylous Limonium kaschgaricum (Plumbaginaceae) [J]. Chin J Plant Ecol, 2021, 45(1): 51-61. |
[2] | Haidong Li, Zongxin Ren, Zhikun Wu, Kun Xu, Hong Wang. Variation in floral traits of distylous Primula poissonii (Primulaceae) along geographic gradients [J]. Biodiv Sci, 2015, 23(6): 747-758. |
[3] | Wei Zhou;Hong Wang . Heterostyly in Angiosperms and Its Evolutionary Significance [J]. Chinese Bulletin of Botany, 2009, 44(06): 742-751. |
[4] | Min Liu, Shan Sun, Qing-jun Li. The relation between stigma position and receptivity in two flexistylous gingers [J]. Biodiv Sci, 2007, 15(6): 639-644. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||