Abstract
Commelina erecta is a successful weed species. The aims of this study were to analyse the morpho-anatomy of the fruit and dimorphic seeds of the weed C. erecta, the dynamics and type of dormancy, and water entry. Flowers and fruits at different development stages were processed using standard anatomical techniques. Besides, experiments of imbibition, germinability and water entry were performed on both seed types. In the fruit of C. erecta, free and coated seeds are developed within dehiscent and indehiscent carpels, respectively. Dehiscent carpels open through a region of mechanical weakness in the dorsal vascular bundle. This region does not form in the indehiscent carpel. The main anatomical differences between the two seed types were observed in the testa and in the number of covering layers. Imbibition experiments showed that the covering of both seed types is water permeable, so these seeds lack physical dormancy and may exhibit physiological dormancy. Germinability experiments showed that the dormancy in free seeds is variable throughout the reproductive season, whereas, in coated seeds, it is high throughout the reproductive season. The embryotega is an area where the hardness of the seed coat is interrupted and facilitates water entry. Differences in the morpho-anatomy of carpels result in the formation of dimorphic seeds with different covering layers and different germination properties. These different properties allow some seeds germinate immediately after falling from the mother plant, and others to be incorporated into the seed bank. These results are useful for designing weed management strategies in agroecosystems.
Similar content being viewed by others
Data availability
Not applicable.
Code availability
Not applicable.
References
Arregui MC, Scotta R, Sánchez D (2006) Improved weed control with broadleaved herbicides in glyphosate-tolerant soybean (Glycine max). J Crop Prot 25:653–656. https://doi.org/10.1016/j.cropro.2005.09.006
Ballester P, Ferrándiz C (2017) Shattering fruits: variations on a dehiscent theme. Curr Opin Plant Biol 35:68–75. https://doi.org/10.1016/j.pbi.2016.11.008
Baskin C, Baskin J (2014) Seeds: ecology, biogeography and evolution of dormancy and germination. Academic Press, San Diego
Baskin J, Baskin C (2021) The great diversity in kinds of seed dormancy: a revision of the Nikolaeva-Baskin classification system for primary seed dormancy. Seed Sci Res 31:249–277. https://doi.org/10.1017/S096025852100026X
Bates D, Mächler M, Bolker B, Walker S (2015) Fitting linear mixed-effects models using lme4. J Stat Soft 67:1–48. https://doi.org/10.18637/jss.v067.i01
Boesewinkel FD, Bouman F (1995) The seed: structure and function. In: Kigel J, Galili G (eds) Seed development and germination. Marcel Dekker, New York, pp 1–24
Bose A, Paria N (2019) Seedling morphology of some selected members of Commelinaceae and its bearing in taxonomic studies. Plant Sci Today 6:218–231. https://doi.org/10.14719/pst.2019.6.2.527
Bregman R, Bouman F (1983) Seed germination in Cactaceae. Bot J Linn Soc 86:357–374. https://doi.org/10.1111/j.1095-8339.1983.tb00977.x
Budd GD, Thomas EL, Allison JCS (1979) Vegetative regeneration depth of germination and seed dormancy in Commelina benghalensis L. Rhod J Agric Res 17:151–153
Cocucci AE (2005) Morphogenetic seed types of Spermatophyta. Pl Syst Evol 250:1–6. https://doi.org/10.1007/s00606-002-0255-4
Costea M, El Miari H, Laczkó L, Fekete R, Molnár AV, Lovas-Kiss Á, Green AJ (2019) The effect of gut passage by waterbirds on the seed coat and pericarp of diaspores lacking “external flesh”: evidence for widespread adaptation to endozoochory in angiosperms. PLoS ONE 14(12):e0226551. https://doi.org/10.1371/journal.pone.0226551
D’Ambrogio de Argüeso A (1986) Manual de Técnicas en Histología Vegetal. Hemisferio Sur .SA., Buenos Aires
da Silva EA, Toorop PE, Nijsse J, Bewley JD, Hilhorst HW (2005) Exogenous gibberellins inhibit coffee (Coffea arabica cv. Rubi) seed germination and cause cell death in the embryo. J Expl Bot 56:1029–1038
Dellaferrera IM, Guarise N, Amsler A (2007) Relevamiento de malezas en cultivos de soja en sistemas de siembra directa con glifosato del departamento de San Justo (Provincia de Santa Fe). Rev FAVE Cienc Agrarias 5/6:15–25. https://doi.org/10.14409/fa.v5i1/2.1318
Evert RF (2006) Esau’s plant anatomy: meristems, cells, and tissues of the plant body: their structure, function, and development. Wiley, Hoboken
Faccini D, Vitta JI (2005) Germination characteristics of Amaranthus quitensis as affected by seed production date and duration of burial. Weed Res 45:371–378. https://doi.org/10.1111/j.1365-3180.2005.00469.x
Faden RB (1998) Commelinaceae. In: Kubitzki K (ed) The Families and Genera of Vascular plants. plants, vol 4. Springer-Verlag, Berlin, pp 109–128
Ferreira MI, Reinhardt CF (1999) The role of temperature in the germination of subterranean and aerial seeds of Commelina benghalensis L. S Afr J Plant Soil 16:165–168. https://doi.org/10.1080/02571862.1999.10635004
Franceschi VR, Nakata PA (2005) Calcium oxalate in plants: formation and function. Annu Rev Plant Biol 56:41–71. https://doi.org/10.1146/annurev.arplant.56.032604.144106
Goddard RH, Webster TM, Carter R, Grey TL (2009) Resistance of Benghal Dayflower (Commelina benghalensis) Seeds to Harsh Environments and the Implications for Dispersal by Mourning Doves (Zenaida macroura) in Georgia, U.S.A. Weed Sci 57:603–612. https://doi.org/10.1614/WS-09-046.1
Goggin DE, Steadman KJ, Emery RN, Farrow SC, Benech-Arnold RL, Powles SB (2009) ABA inhibits germination but not dormancy release in mature imbibed seeds of Lolium rigidum Gaud. J Exp Bot 60:3387–3396
Grootjen CJ (1983) Development of ovule and seed in Cartonema spicatum R. Br. (Cartonemataceae). Aust J Bot 31:297–305. https://doi.org/10.1071/BT9830297
Gupta R, Chakrabarty SK (2013) Gibberellic acid in plant: still a mystery unresolved. Plant Signal Behav 8:e25504
Hassani SB, Saboora A, Radjabian T, Fallah Husseini H (2009) Effects of temperature, GA3 and cytokinins on breaking seed dormancy of Ferula assafoetida L. Iran J Sci Technol (sciences) 33:75–85
Hassemer G (2019) Further advances to the nomenclatural, taxonomic and geographic knowledge of the New World Commelina (Commelinaceae): toward a continental treatment. Phytotaxa 400:89–122. https://doi.org/10.11646/phytotaxa.400.3.1
Hu XW, Pan J, Min DD, Fan Y, Ding XY, Fan SG, Baskin CC, Baskin JM (2017) Seed dormancy and soil seedbank of the invasive weed Chenopodium hybridum in north-western China. Weed Res 57:54–64. https://doi.org/10.1111/wre.12237
Huss JC, Gierlinger N (2021) Functional packaging of seeds. New Phytol 230:2154–2163. https://doi.org/10.1111/nph.17299
ISTA (2008) International rules for seed testing. International. Seed Testing Association, Bassersdorf
Jang BK, Park K, Lee SY, Lee H, Song SK, Kim J, Hee C, Cho JS (2023) Comparison of the seed dormancy and germination characteristics of six Clematis species from south Korea. Sci Hortic 307:111488
Johansen DA (1940) Plant Microtechnique. McGraw-Hill Book Co, New York
Johri BM, Ambegaokar KB, Srivastava PS (1992) Comparative embryology of angiosperms, vol 2. Springer-Verlag, Berlin
Kraus TA, Grosso MA, Basconsuelo SC, Bianco CA, Malpassi RN (2007) Morphology and anatomy of shoot, root, and propagation systems in Hoffmannseggia glauca. Plant Biol 9:705–712. https://doi.org/10.1055/s-2007-965080
Küster E (1956) Die Pfl anzenzelle, 3rd edn. Gustav Fischer Verlag, Jena
Lee SY, Park K, Jang BK, Ji B, Lee H, Baskin CC, Cho JS (2022) Exogenous gibberellin can effectively and rapidly break intermediate physiological dormancy of Amsonia elliptica seeds. Front Plant Sci 13:1043897. https://doi.org/10.3389/fpls.2022.1043897
Luque R, Sousa HC, Kraus JE (1996) Métodos de coloração de Roeser (1972) -modificado- e Kropp (1972) visando a substituição do azul de astra por azul de alcião 8 GS ou 8GX. Acta Bot Brasil 10:199–212. https://doi.org/10.1590/S0102-33061996000200001
Matsuo M, Michinaga H, Terao H, Tsuzuki E (2004) Aerial seed germination and morphological characteristics of juvenile seedlings in Commelina benghalensis L. Weed Biol Manag 4:148–153. https://doi.org/10.1111/j.1445-6664.2004.00135.x
Mummenhoff K, Polster A, Mühlhausen A, Theißen G (2009) Lepidiumas amodelsystem for studying the evolution of fruit development in Brassicaceae. J Exp Bot 60:1503–1513
Murgia ML, Attene G, Rodriguez M, Bitocchi E, Bellucci E, Fois D, Nanni L, Gioia T, Albani DM, Papa R, Rau D (2017) A comprehensive phenotypic investigation of the “pod-shattering syndrome” in common bean. Front Plant Sci 8:251. https://doi.org/10.3389/fpls.2017.00251
Nikolaeva MG (1977) Factors controlling the seed dormancy pattern. In: Khan AA (ed) The physiology and biochemistry of seed dormancy and germination. Amsterdam, North-Holland, pp 51–74
Nisensohn LA, Tuesca DH, Vitta JI (2011) Características reproductivas de Commelina erecta L. asociadas con su propagación en sistemas agrícolas. Agriscientia 28:51–60. https://doi.org/10.31047/1668.298x.v28.n1.2784
Orozco-Segovia A, Márquez-Guzmán J, Sánchez-Coronado ME, Gamboa de Buen A, Baskin JM, Baskin CC (2007) Seed anatomy and water uptake in relation to seed dormancy in Opuntia tomentosa (Cactaceae, Opuntioideae). Ann Bot 99:581–592. https://doi.org/10.1093/aob/mcm001
Panigo ES, Dellaferrera IM, Acosta JM, Bender AG, Garetto JI, Perreta MG (2012) Glyphosate-induced structural variations in Commelina erecta L. (Commelinaceae). Ecotoxicol Environ Saf 76:135–142. https://doi.org/10.1016/j.ecoenv.2011.10.002
Panigo ES, Nisensohn LA (2018) Commelina erecta L. In: Fernández O, Leguizamón, ES, Acciaresi HA, Troiani HO, Villamil CB (eds). Malezas e invasoras de la Argentina. Tomo III: historia y biología. EdiUNS, Bahía Blanca, pp 181–190
Panigo ES, Dellaferrera IM, Olivella J, Chantre GR, Sabbatini MR, Perreta MG (2015) Comportamiento germinativo de dos poblaciones de Commelina erecta L. con diferente historia productiva. Resumen. Libro de resumen del XXII Congreso Latinoamericano de Malezas (ALAM) y I Congreso Argentino de Malezas (ASACIM), pp 148
Panigo ES, Gisbert A, Dellaferrera IM, Perreta MG (2021) Effect of different post-ripening treatments on the germination of Commelina erecta L. ovoid seeds. Resumen. Bol Soc Argent Bot Suplemento 56:122–123
Pearse AGE (1985) Histochemistry: theoretical and applied, 4th edn, vol 2. Analytical technology. Churchill Livingstone, Edinburgh
Pellegrini MO, Forzza RC (2017) Synopsis of Commelina L. (Commelinaceae) in the state of Rio de Janeiro, reveals a new white-flowered species endemic to Brazil. PhytoKeys 78:59–81. https://doi.org/10.3897/phytokeys.78.11932
Pereira MP, Corrêa FF, Polo M, de Castro EM, Cardoso AÁ, Pereira FJ (2016) Seed germination of Schinus molle L. (Anacardiaceae) as related to its anatomy and dormancy alleviation. Seed Sci Res 26:351–361. https://doi.org/10.1017/S0960258516000167
Puente R, Faden RB (2001) Commelinaceae Spiderwort Family. J Arizona-Nevada Acad Sci 33:19–26
R Core Team (2022) R: a language and environment for statistical computing. R Vienna: Foundation for Statistical Computing. Available at: http://www.R-project.org/. Accessed 26 Sept 2022
Ritz C, Streibig JC (2005) Bioassay analysis using R. J Stat Softw 12:1–22
Roth I (1977) Fruits of Angiosperms. In: Linsbauer K (ed) Encyclopedia of Plant Anatomy. Gebrüder Borntraeger, Berlin, pp 148–194
Ruzin SE (1999) Plant microtechnique and microscopy. Oxford University Press, Oxford
Spjut RW (1994) A systematic treatment of fruit types. Mem N Y Bot Gard 70:1–182
Steedman HF (1950) Alcian Blue 8GS: a new stain for mucin. J Cell Sci 91:477–479. https://doi.org/10.1242/jcs.s3-91.16.477
Streibig JC, Kudsk P (1993) Herbicide bioassays. CRC Press Inc, Boca Ratón
Takhtajan AL (1985) Comparative anatomy of the seeds, vol. 1: monocotyledons. Nauka Press, Leningrad
Walker SR, Evenson JP (1985) Biology of Commelina benghaiensis L. in south-eastern Queensland. Seed dormancy, germination and emergence. Weed Res 25:245–250. https://doi.org/10.1111/j.1365-3180.1985.tb00641.x
Wilson JA (1981) Stomatal responses to ABA and COj in epidermis detached from well-watered and water-stressed plants of Commelina communis L. J Exp Bot 32:261–269. https://doi.org/10.1093/jxb/32.1.261
Acknowledgements
The authors thank Dr. Raúl Pozner for critical reading of the manuscript.
Funding
This work was supported by the Agencia Nacional de Promoción Científica y Tecnológica, Argentina (PICT 2018–03944 to MGP) and Universidad Nacional del Litoral, Santa Fe, Argentina (CAI + D2020-50520190100078LI to AGR and CAI + D2016-50020150100015LI to ESP).
Author information
Authors and Affiliations
Contributions
ESP, AGR, MGP, and GRC conceived and designed research. ESP, AGR, and MGP procured funding. ESP, AGR, EO and IMD collected samples in the field and conducted experiments. All authors analyzed data. ESP and AGR wrote the manuscript, and prepared figures. All authors read and approved the final manuscript.
Corresponding authors
Ethics declarations
Ethics approval
Not applicable.
Consent to participate
All authors have seen and agree with the content of this manuscript.
Consent for publication
All authors agree with the publication of this manuscript.
Competing interests
The authors declare no competing interests.
Additional information
Handling Editor: Peter Nick
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
709_2023_1904_MOESM1_ESM.pdf
Supplementary file1 ESM 1 Ovule development, megasporogenesis and megagametogenesis in Commelina erecta. (a) and (b) ovule primordium in which the megasporocyte, and the inner and outer integuments primordium can be recognized; note the advanced growth of the inner tegument compared to the outer tegument (c) and (d) megaspores tetrad with the three micropylar megaspores degenerating, and the chalazal one enlarged; the inner integument grows more rapidly than the outer integument, completely surrounding the nucellus and delimiting the micropyle (e–h) successive stages of megagametophyte formation; an eight-nucleate Polygonum-type embryo sac is observed at ripe stage. Abbreviations: an antipodal cell, cc central cell, dm degenerate megaspores, fm functional megaspore, ii inner integument, m micropyle, mc megasporocyte, mp micropylar pole, n nucellus, oi outer integument, ov ovary wall, s embryo sac, sy synergid cell, te megaspores tetrad. Scale bars: a = 20 µm; b, d-f, h = 30 µm; c, g = 100 µm. (PDF 2752 kb)
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Panigo, E.S., Oggero, E., Dellaferrera, I.M. et al. Fruit dehiscence mechanism and release of dimorphic seeds with different germination properties in Commelina erecta. Protoplasma 261, 377–393 (2024). https://doi.org/10.1007/s00709-023-01904-z
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00709-023-01904-z