Narcy Anai Pereira-Zaldívar, Luis David Patiño-López, Raúl Rodríguez-García, José Luis Andrade, Manuel Jesús Cach-Pérez, Celene Espadas-Manrique, Felipe Barredo-Pool, Casandra Reyes-García
{"title":"在大气附生凤梨科植物中,由毛状体介导的外部水分输送可能补偿了维管效率的降低。","authors":"Narcy Anai Pereira-Zaldívar, Luis David Patiño-López, Raúl Rodríguez-García, José Luis Andrade, Manuel Jesús Cach-Pérez, Celene Espadas-Manrique, Felipe Barredo-Pool, Casandra Reyes-García","doi":"10.1071/FP25140","DOIUrl":null,"url":null,"abstract":"<p><p>Complex trichomes in the leaves of epiphytic Bromeliaceae absorb water and nutrients, while also facilitating long distance water transport along the leaf surface, a phenomenon previously characterized for two Tillandsia species. This study aimed to determine trichome traits that govern external water transport speed, and its relation to life form, xylem transport capacity and environmental conditions. Using near-infrared optical techniques, we characterized trichome-mediated transport in 19 species and analyzed its association with trichome and vascular traits, functional group, and habitat parameters. External leaf water transport was observed in 10 species, all of which were atmospheric life forms (nebulophytes and pseudobulbs). Transport speed positively correlated with trichome area, wing length, and degree of overlap. Species with higher trichome overlap had lower xylem capacity (Kx ) and tracheid diameter and numbers, suggesting that the atmospheric life form is related to secure, inefficient vascular systems, which may be partly compensated with external transport. External transport was more common in species from habitats with high maximum vapor pressure deficits and low aridity indices, suggesting it enhances water uptake by rapidly redistributing water across available trichomes before evaporation can occur.</p>","PeriodicalId":12483,"journal":{"name":"Functional Plant Biology","volume":"52 ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Trichome mediated external water transport may compensate for reduced vascular efficiency in atmospheric epiphytic Bromeliaceae.\",\"authors\":\"Narcy Anai Pereira-Zaldívar, Luis David Patiño-López, Raúl Rodríguez-García, José Luis Andrade, Manuel Jesús Cach-Pérez, Celene Espadas-Manrique, Felipe Barredo-Pool, Casandra Reyes-García\",\"doi\":\"10.1071/FP25140\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Complex trichomes in the leaves of epiphytic Bromeliaceae absorb water and nutrients, while also facilitating long distance water transport along the leaf surface, a phenomenon previously characterized for two Tillandsia species. This study aimed to determine trichome traits that govern external water transport speed, and its relation to life form, xylem transport capacity and environmental conditions. Using near-infrared optical techniques, we characterized trichome-mediated transport in 19 species and analyzed its association with trichome and vascular traits, functional group, and habitat parameters. External leaf water transport was observed in 10 species, all of which were atmospheric life forms (nebulophytes and pseudobulbs). Transport speed positively correlated with trichome area, wing length, and degree of overlap. Species with higher trichome overlap had lower xylem capacity (Kx ) and tracheid diameter and numbers, suggesting that the atmospheric life form is related to secure, inefficient vascular systems, which may be partly compensated with external transport. External transport was more common in species from habitats with high maximum vapor pressure deficits and low aridity indices, suggesting it enhances water uptake by rapidly redistributing water across available trichomes before evaporation can occur.</p>\",\"PeriodicalId\":12483,\"journal\":{\"name\":\"Functional Plant Biology\",\"volume\":\"52 \",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Functional Plant Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1071/FP25140\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Functional Plant Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1071/FP25140","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Trichome mediated external water transport may compensate for reduced vascular efficiency in atmospheric epiphytic Bromeliaceae.
Complex trichomes in the leaves of epiphytic Bromeliaceae absorb water and nutrients, while also facilitating long distance water transport along the leaf surface, a phenomenon previously characterized for two Tillandsia species. This study aimed to determine trichome traits that govern external water transport speed, and its relation to life form, xylem transport capacity and environmental conditions. Using near-infrared optical techniques, we characterized trichome-mediated transport in 19 species and analyzed its association with trichome and vascular traits, functional group, and habitat parameters. External leaf water transport was observed in 10 species, all of which were atmospheric life forms (nebulophytes and pseudobulbs). Transport speed positively correlated with trichome area, wing length, and degree of overlap. Species with higher trichome overlap had lower xylem capacity (Kx ) and tracheid diameter and numbers, suggesting that the atmospheric life form is related to secure, inefficient vascular systems, which may be partly compensated with external transport. External transport was more common in species from habitats with high maximum vapor pressure deficits and low aridity indices, suggesting it enhances water uptake by rapidly redistributing water across available trichomes before evaporation can occur.
期刊介绍:
Functional Plant Biology (formerly known as Australian Journal of Plant Physiology) publishes papers of a broad interest that advance our knowledge on mechanisms by which plants operate and interact with environment. Of specific interest are mechanisms and signal transduction pathways by which plants adapt to extreme environmental conditions such as high and low temperatures, drought, flooding, salinity, pathogens, and other major abiotic and biotic stress factors. FPB also encourages papers on emerging concepts and new tools in plant biology, and studies on the following functional areas encompassing work from the molecular through whole plant to community scale. FPB does not publish merely phenomenological observations or findings of merely applied significance.
Functional Plant Biology is published with the endorsement of the Commonwealth Scientific and Industrial Research Organisation (CSIRO) and the Australian Academy of Science.
Functional Plant Biology is published in affiliation with the Federation of European Societies of Plant Biology and in Australia, is associated with the Australian Society of Plant Scientists and the New Zealand Society of Plant Biologists.