{"title":"是什么保持了花柱的张力?通过实验测试了解马兰头花科植物爆发性花柱运动的生物力学。","authors":"Marcus Jerominek, Regine Claßen-Bockhoff","doi":"10.1007/s10265-024-01535-2","DOIUrl":null,"url":null,"abstract":"<p><p>Pollination in Marantaceae is mediated by an explosive style movement. Before release, style tension is held by the hooded staminode. When a pollinator touches the trigger appendage of the hooded staminode the latter deforms and the style rapidly curls upwards. This movement has been interpreted as a turgor movement by some authors, but recent studies clearly indicate that setup, hold and release of tension are purely mechanical processes. However, in view of the high diversity of hooded staminodes, the question arises what keeps the tension in species with very thin staminodes. To test the holding mechanisms, we conducted mechanical and physico-chemical release experiments in four species with robust and four species with thin hooded staminodes in their natural tropical environment. We found almost the same response of all species to mechanical treatments, but species-specific reactions to different physico-chemical conditions. This indicates that style release follows the same mechanical principles in all species, but that the sensitivity of the explosive movement depends on material properties like tissue thickness and turgescence. As to the holding mechanisms, we found different degrees of floral synorganization. The hood of the hooded staminode formerly interpreted as an important holding structure does not play a noteworthy role. Instead, the basal plate of the hooded staminode antagonises the pressure of the style head against the holding point of the hooded staminode in species with robust hooded staminodes and well-developed basal plates. In some species with a thin hooded staminode, the latter is closely attached to the style and most likely stabilises tension by adhesive forces. In another species, a morphologically analogous structure adopts the function of the basal plate. We conclude that the holding mechanism of the style tension diversified during the evolution of Marantaceae whereas the release mechanism itself has been conserved throughout the family.</p>","PeriodicalId":16813,"journal":{"name":"Journal of Plant Research","volume":" ","pages":"745-762"},"PeriodicalIF":2.7000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"What keeps the style under tension? Experimental tests to understand the biomechanics of the explosive style movement in Marantaceae.\",\"authors\":\"Marcus Jerominek, Regine Claßen-Bockhoff\",\"doi\":\"10.1007/s10265-024-01535-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Pollination in Marantaceae is mediated by an explosive style movement. Before release, style tension is held by the hooded staminode. When a pollinator touches the trigger appendage of the hooded staminode the latter deforms and the style rapidly curls upwards. This movement has been interpreted as a turgor movement by some authors, but recent studies clearly indicate that setup, hold and release of tension are purely mechanical processes. However, in view of the high diversity of hooded staminodes, the question arises what keeps the tension in species with very thin staminodes. To test the holding mechanisms, we conducted mechanical and physico-chemical release experiments in four species with robust and four species with thin hooded staminodes in their natural tropical environment. We found almost the same response of all species to mechanical treatments, but species-specific reactions to different physico-chemical conditions. This indicates that style release follows the same mechanical principles in all species, but that the sensitivity of the explosive movement depends on material properties like tissue thickness and turgescence. As to the holding mechanisms, we found different degrees of floral synorganization. The hood of the hooded staminode formerly interpreted as an important holding structure does not play a noteworthy role. Instead, the basal plate of the hooded staminode antagonises the pressure of the style head against the holding point of the hooded staminode in species with robust hooded staminodes and well-developed basal plates. In some species with a thin hooded staminode, the latter is closely attached to the style and most likely stabilises tension by adhesive forces. In another species, a morphologically analogous structure adopts the function of the basal plate. We conclude that the holding mechanism of the style tension diversified during the evolution of Marantaceae whereas the release mechanism itself has been conserved throughout the family.</p>\",\"PeriodicalId\":16813,\"journal\":{\"name\":\"Journal of Plant Research\",\"volume\":\" \",\"pages\":\"745-762\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Plant Research\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s10265-024-01535-2\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/3/27 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Plant Research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s10265-024-01535-2","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/3/27 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
What keeps the style under tension? Experimental tests to understand the biomechanics of the explosive style movement in Marantaceae.
Pollination in Marantaceae is mediated by an explosive style movement. Before release, style tension is held by the hooded staminode. When a pollinator touches the trigger appendage of the hooded staminode the latter deforms and the style rapidly curls upwards. This movement has been interpreted as a turgor movement by some authors, but recent studies clearly indicate that setup, hold and release of tension are purely mechanical processes. However, in view of the high diversity of hooded staminodes, the question arises what keeps the tension in species with very thin staminodes. To test the holding mechanisms, we conducted mechanical and physico-chemical release experiments in four species with robust and four species with thin hooded staminodes in their natural tropical environment. We found almost the same response of all species to mechanical treatments, but species-specific reactions to different physico-chemical conditions. This indicates that style release follows the same mechanical principles in all species, but that the sensitivity of the explosive movement depends on material properties like tissue thickness and turgescence. As to the holding mechanisms, we found different degrees of floral synorganization. The hood of the hooded staminode formerly interpreted as an important holding structure does not play a noteworthy role. Instead, the basal plate of the hooded staminode antagonises the pressure of the style head against the holding point of the hooded staminode in species with robust hooded staminodes and well-developed basal plates. In some species with a thin hooded staminode, the latter is closely attached to the style and most likely stabilises tension by adhesive forces. In another species, a morphologically analogous structure adopts the function of the basal plate. We conclude that the holding mechanism of the style tension diversified during the evolution of Marantaceae whereas the release mechanism itself has been conserved throughout the family.
期刊介绍:
The Journal of Plant Research is an international publication that gathers and disseminates fundamental knowledge in all areas of plant sciences. Coverage extends to every corner of the field, including such topics as evolutionary biology, phylogeography, phylogeny, taxonomy, genetics, ecology, morphology, physiology, developmental biology, cell biology, molecular biology, biochemistry, biophysics, bioinformatics, and systems biology.
The journal presents full-length research articles that describe original and fundamental findings of significance that contribute to understanding of plants, as well as shorter communications reporting significant new findings, technical notes on new methodology, and invited review articles.