High resilience to extreme climatic changes in the CAM epiphyte Tillandsia utriculata L. (Bromeliaceae).
Journal
Physiologia plantarum
ISSN: 1399-3054
Titre abrégé: Physiol Plant
Pays: Denmark
ID NLM: 1256322
Informations de publication
Date de publication:
Mar 2020
Mar 2020
Historique:
received:
12
02
2018
revised:
09
07
2018
accepted:
12
07
2018
pubmed:
24
8
2018
medline:
25
3
2020
entrez:
24
8
2018
Statut:
ppublish
Résumé
Climate change is expected to increase the frequency of extreme climatic events, yet few studies have addressed the capacity of plant species to deal with such events. Species that are widespread are predicted to be highly plastic and able to acclimate to highly changing conditions. To study the plasticity in physiological responses of the widely distributed epiphyte Tillandsia utriculata, we transplanted individuals from a coastal scrub and broadleaf evergreen forest to a similar coastal scrub site and forest. After a 45-day acclimation, the plants were moved to a semi-controlled greenhouse at each site, and then subjected to a 20-day drought. Physiological variables were measured during the acclimation and the drought. The individuals of scrub and forest populations had similar relative water content and carbon assimilation in the contrasting conditions of the two transplantation sites despite the high discrepancy between the environments at their original site. Electron transport rates were higher in individuals from the scrub population. Electron transport rates were also higher than estimated from carbon assimilation, suggesting that photorespiration was present. The individuals of the coastal scrub population had a higher capacity to dissipate excess energy this way. The relative distance index of plasticity was high overall, indicating that some traits are highly plastic (titratable acidity, carbon assimilation) in order to maintain the stability of others (maximum quantum yield F
Substances chimiques
Water
059QF0KO0R
Carbon
7440-44-0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
547-562Subventions
Organisme : SEP-CONACYT
ID : 80181
Organisme : SEP-CONACYT
ID : 221490
Organisme : INEGI-CONACYT
ID : 290916
Informations de copyright
© 2018 Scandinavian Plant Physiology Society.
Références
Ackerly DD (2003) Community assembly, niche conservatism, and adaptive evolution in changing environments. Int J Plant Sci 164: 165-184
Angert AL, Schemske DW (2005) The evolution of species' distributions: reciprocal transplants across the elevation ranges of Mimulus cardinals and M. lewisii. Evolution 59: 1671-1684
Bader MY, Menke G, Zotz G (2009) Pronounced drought tolerance characterizes the early life stages of the epiphytic bromeliad Tillandsia flexuosa. Funct Ecol 23: 472-479
Baker HG (1965) Characteristics and modes of origin of weeds. In: Baker HG, Stebbins GL (eds) The Genetics of Colonizing Species. Academic Press, New York, pp 147-168
Baquedano FJ, Valladares F, Castillo FJ (2008) Phenotypic plasticity blurs ecotypic divergence in the response of Quercus coccifera and Pinus halepensis to water stress. Eur J For Res 127: 495-506
Benzing DH (2000) Bromeliaceae: Profile of an Adaptive Radiation. Cambridge University Press, Cambridge
Benzing DH, Renfrow A (1971) The significance of photosynthetic efficiency to habitat preference and phylogeny among Tillandsioid bromeliads. Bot Gaz 132: 19-30
Bilger W, Björkman O (1990) Role of the xanthophyll cycle in photoprotection elucidated by measurements of light-induced absorbance changes, fluorescence and photosynthesis in Hedera canariensis. Photosynth Res 25: 173-185
Borland AM, Griffiths H (1989) The regulation of citric acid accumulation and carbon recycling during CAM in Ananas comosus. J Exp Bot 40: 53-60
Brock MT, Weinig C, Galen C (2005) A comparison of phenotypic plasticity in the native dandelion Taraxacum ceratophorum and its invasive congener T. officinale. New Phytol 166: 173-183
Cach-Pérez MJ, Andrade JL, Chilpa-Galván N, Tamayo-Chim M, Orellana R, Reyes-García C (2013) Climatic and structural factors influencing epiphytic bromeliad community assemblage along a gradient of water-limited environments in the Yucatan Peninsula, Mexico. Trop Conserv Sci 6: 283-302
Cach-Pérez MJ, Andrade JL, Cetzal-Ix W, Reyes-García C (2016) Environmental influence on the inter- and intraspecific variation in the density and morphology of stomata and trichomes of epiphytic bromeliads of the Yucatan Peninsula. Bot J Linn Soc 181: 441-458
Cach-Pérez MJ, Andrade JL, Reyes-García C (2018) Morphophysiological plasticity in epiphytic bromeliads across a precipitation gradient in the Yucatan Peninsula, Mexico. Trop Conserv Sci 11: 1940082918781926
Carvajal DE, Loayza AP, Rios RS, Gianoli E, Squeo FA (2017) Population variation in drought-resistance strategies in a desert shrub along an aridity gradient: interplay between phenotypic plasticity and ecotypic differentiation. Perspect Plant Ecol Evol Syst 29: 12-19
Centro de Investigación Científica de Yucatán Herbarium 2017. Available at <http://www.cicy.mx/unidad-de-recursos-naturales/herbario> (accessed 20 November 2017)
Chaves CJN, Leal BSS, de Lemos-Filho JP (2017) How are endemic and widely distributed bromeliads responding to warming temperatures? A case study in a Brazilian hotspot. Flora 238: 110-118
Chazdon R, Kaufmann S (1993) Plasticity of leaf anatomy of two rainforest shrubs in relation to photosynthetic light acclimation. Funct Ecol 7: 385-394
Cook B, Smerdon J, Seager R, Coats S (2014) Global warming and 21st century drying. Climate Dynam 43: 1-21
Crayn DM, Winter K, Smith JAC (2004) Multiple origins of crassulacean acid metabolism and the epiphytic habit in the Neotropical family Bromeliaceae. Proc Natl Acad Sci USA 101: 3703-3708
Easterling DR, Meehl GA, Parmesan C, Changnon SA, Karl TR, Mearns LO (2000) Climate extremes: observations, modeling and impacts. Science 289: 2068-2074
Freschi L, Takahashi CA, Cambui CA, Semprebom TR, Cruz AB, Mioto PT, Versieux LM, Calvente A, Latansio-Aidar SR, Aidar MPM, Mercier H (2010) Specific leaf areas of the tank bromeliad Guzmania monostachia perform distinct functions in response to water shortage. J Plant Physiol 167: 526-533
Genty B, Briantais JM, Baker NR (1989) The relationship between quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990: 87-92
Gianoli F (2004) Plasticidad fenotípica adaptativa en plantas. In: Marino H (ed) Fisiología Ecológica en Plantas. Ediciones Universitarias de Valparaíso, Mecanismos y Respuestas a Estrés en Ecosistemas, pp 13-25
Godoy O, Valladares F, Castro-Díez P (2011) Multispecies comparison reveals that invasive and native plants differ in their traits but not in their plasticity. Funct Ecol 25: 1248-1259
Godoy O, Valladares F, Castro-Díez P (2012) The relative importance for plant invasiveness of trait means, and their plasticity and integration in a multivariate framework. New Phytol 195: 912-922
González-Salvatierra C, Andrade JL, Orellana R, Peña-Rodríguez LM, Reyes-García C (2013) Microambiente lumínico y morfología y fisiología foliar de Bromelia karatas (Bromeliaceae) en una selva baja caducifolia de Yucatán, México. Bot Sci 91: 75-84
Graham EA, Andrade JL (2004) Drought tolerance associated with vertical stratification of two co-occurring epiphytic bromeliads in a tropical dry forest. Am J Bot 91: 699-706
Grassein F, Till-Bottraud I, Lavorel S (2010) Plant resource-use strategies: the importance of phenotypic plasticity in response to a productivity gradient for two subalpine species. Ann Bot 106: 637-645
Griffith TM, Sultan SE (2005) Shade tolerance plasticity in response to neutral vs green shade cues in Polygonum species of contrasting ecological breadth. New Phytol 166: 141-148
Griffiths H (1989) Crassulacean acid metabolism: a re-appraisal of physiological plasticity in form and function. Adv Bot Res 15: 43-92
Griffiths H, Lüttge U, Stimmel KH, Crook CE, Griffiths NM, Smith JAC (1986) Comparative ecophysiology of CAM and C3 bromeliads. III. Environmental influences on CO2 assimilation and transpiration. Plant Cell Environ 9: 385-393
Griffiths H, Smith JA, Lüttge U, Popp M, Cram WJ, Diaz M, Lee HS, Medina E, Schäfer C, Stimmel KH (1989) Ecophysiology of xerophytic and halophytic vegetation of a coastal alluvial plain in northern Venezuela. New Phytol 111: 273-282
Haslam R, Borland AM, Maxwell K, Griffiths H (2003) Physiological response of CAM epiphyte Tillandsia usneoides L. (Bromeliaceae) to variations in light and water supply. J Plant Physiol 160: 627-634
Herbario Nacional de México. 2018. Universidad Nacional Autónoma de México. Available at http://www.ib.unam.mx/botanica/herbario/ (accessed 15 May 2018)
Jones H (1992) Plant and Microclimate: A Quantitative Approach to Environmental Plant Physiology. Cambridge University Press, Cambridge
Jump AS, Peñuelas J (2005) Running to stand still: adaptation and the response of plants to rapid climate change. Ecol Lett 8: 1010-1020
de la Rosa-Manzano E, Andrade JL, Zotz G, Reyes-García C (2017) Physiological plasticity of epiphytic orchids from two contrasting tropical dry forests. Acta Oecol 85: 25-32
Laube S, Zotz G (2003) Which abiotic factors limit vegetative growth in a vascular epiphyte? Funct Ecol 17: 598-604
Luther HE (2012) An Alphabetical List of Bromeliad Binomials, 30th Edn. Marie Selby Botanical Gardens and Bromeliad Society International, Sarasota, Florida
Martin CE, Adams WW (1987) Crassulacean acid metabolism, CO2-recycling, and tissue desiccation in the Mexican epiphyte Tillandsia schiedeana Steud (Bromeliaceae). Photosynth Res 11: 237-244
Martin CE, Christensen NL, Strain BR (1981) Seasonal patterns of growth, tissue acid fluctuations, and 14CO2 uptake in the crassulacean acid metabolism epiphyte Tjllandsia usneoides L. (Spanish moss). Oecologia 49: 322-328
Martin CE, Eades CA, Pitner RA (1986) Effects on crassulacean acid metabolism in the epiphyte Tillandsia usneoides L. (Bormeliaceae). Plant Physiol 80: 23-26
Martin CE, Tüffers A, Herppich WB, von Willert DJ (1999) Utilization and dissipation of absorbed light energy in the epiphytic crassulacean acid metabolism bromeliad Tillandsia ionantha. Int J Plant Sci 160: 307-313
Maxwell K (2002) Resistance is useful: diurnal patterns of photosynthesis in C3 and crassulacean acid metabolism epiphytic bromeliads. Funct Plant Biol 29: 679-687
Miner BG, Sultan SE, Morgan SG, Padilla DK, Relyea RA (2005) Ecological consequences of phenotypic plasticity. Trends Ecol Evolut 20: 685-692
Niewiadomska E, Borland AM (2008) Crassulacean acid metabolism: a cause or consequence of oxidative stress in planta? In: Lüttge U (ed) Progress in Botany. Springer, Berlin, pp 247-266
Oliva G, Martinez A, Collantes M, Dubcovsky J (1993) Phenotypic plasticity and contrasting habitat colonization in Festuca pallescens. Can J Bot 71: 970-977
Palacio K, Rodríguez N (2007) Plasticidad fenotípica en Lippia alba (Verbenaceae) en respuesta a la disponibilidad hídrica en dos ambientes lumínicos. Acta Biol Colomb 12: 187-198
Palacio-López K, Gianoli E (2011) Invasive plants do not display greater phenotypic plasticity than their native or non-invasive counterparts: a meta-analysis. Oikos 120: 1393-1401
Parra E, Rodríguez N (2007) Plasticidad fenotípica de Lippia alba y Lippia origanoides (Verbenaceae) en respuesta a la disponibilidad de luz. Acta Biol Colomb 12: 91-102
Pett-Ridge J, Silver WL (2002) Survival, growth and ecosystem dynamics of displaced bromeliads in montane tropical forest. Biotropica 34: 211-224
Pinzón JP, Ramírez IM, Carnevali G (2011) Morphometric analyses within the Tillandsia utriculata L. complex (Bromeliaceae) allow for the recognition of a new species, with notes on its phylogenetic position. J Torrey Bot Soc 138: 353-365
Pinzón JP, Ramírez-Morillo IM, Carnevali G, Barfuss MH, Till W, Tun J, Ortiz-Díaz JJ (2016) Phylogenetics and evolution of the Tillandsia utriculata complex (Bromeliaceae, Tillandsioideae) inferred from three plastid DNA markers and the ETS of the nuclear ribosomal DNA. Bot J Linn Soc 181: 362-390
Pires MV, de Almeida AAF, Abreu PP, da Costa SD (2012) Does shading explain variation in morphophysiological traits of tropical epiphytic orchids grown in artificial conditions? Acta Physiol Plant 34: 2155-2164
Pompelli MF, Pompelli MG, Cabrini EC, Alves MCJL, Ventrella MC (2012) Leaf anatomy, ultrastructure and plasticity of Coffea arabica L. in response to light and nitrogen. Biotemas 25: 13-28
Ramírez IM, Carnevali G, Chi F (2004) Guía Ilustrada de las Bromeliaceae de la Porción Mexicana de la Península de Yucatán. Centro de Investigación científica de Yucatán. A.C. México, México
Ran F, Zhang X, Zhang Y, Korpelainen H, Li C (2013) Altitudinal variation in growth, photosynthetic capacity and water use efficiency of Abies faxoniana Rehd. et Wils. Seedlings as revealed by reciprocal transplantations. Trees 27: 1405-1416
Rascher U, Liebig M, Lüttge U (2000) Evaluation of instant light response curves of chlorophyll fluorescence parameters obtained with a portable chlorophyll fluorometer on site in the field. Plant Cell Environ 23: 1397-1405
Reyes-García C, Mejia-Chang M, Griffiths H (2012) High but not dry: diverse epiphytic bromeliad adaptations to exposure within a seasonally dry tropical forest community. New Phytol 193: 745-754
Rozendaal DMA, Hurtado VH, Poorter L (2006) Plasticity in leaf traits of 38 tropical tree species in response to light; relationships with light demand and adult stature. Funct Ecol 20: 207-216
Schumacher E, Kueffer C, Edwards PJ, Dietz H (2009) Influence of light and nutrient conditions on seedling growth of native and invasive trees in the Seychelles. Biol Invasions 11: 1941-1954
Secretaría de Gobernación, SEGOB (2003) Enciclopedia de los municipios de México. Instituto Nacional para el Federalismo y el Desarrollo Municipal (INAFED), Sistema Nacional de Información Municipal, México, Chiapas
Skillman JB, Winter K (1997) High photosynthetic capacity in a shade-tolerant crassulacean acid metabolism plant (implications for sunfleck use, nonphotochemical energy dissipation, and susceptibility to photoinhibition). Plant Physiol 113: 441-450
Smith JAC (1989) Epiphytic bromeliads. In: Lüttge U (ed) Vascular Plants as Epiphytes: Evolution and Ecophysiology. Springer, Berlin, pp 109-138
Smith JAC, Lüttge U (1985) Day-night changes in leaf water relations associated with the rhythm of crassulacean acid metabolism in Kalanchoë daigremontiana. Planta 163: 272-282
Spalding MH, Stumpf DK, Ku MSB, Burris RH, Edwards GE (1979) Crassulacean acid metabolism and diurnal variations of internal CO2 and O2 concentrations in Sedum praealtum DC. Funct Plant Biol 6: 557-567
Stiles KC, Martin CE (1996) Effects of drought stress on CO2 exchange and water relations in the CAM epiphyte Tillandsia utriculata (Bromeliaceae). J Plant Physiol 149: 721-728
Sultan SE (2001) Phenotypic plasticity for fitness components in Polygonum species of contrasting ecological breadth. Ecology 82: 328-343
Thomas CD, Cameron A, Green RE, Bakkenes M, Beaumont LJ, Collingham YC, Erasmus BFN, de Siqueira MF, Grainger A, Hannah L, Hughes L, Huntley B, van Jaarsveld AS, Midgley GF, Miles L, Ortega-Huerta MA, Peterson AT, Phillips OL, Williams SE (2004) Extinction risk from climate change. Nature 427: 145-148
Thompson JD, McNeilly T, Gray AJ (1991) Population variation in Spartina anglica Hubbard, C.E. .2. Reciprocal transplants among 3 successional populations. New Phytol 117: 749-763
Thuiller W, Araujo MB, Pearson RG, Whittaker RJ, Brotons L, Lavorel S (2004) Biodiversity conservation: uncertainty in predictions of extinction risk. Nature 430: 145-148
Tropicos 2012. Missouri Botanical Garden. Available at <http://www.tropicos.org/Name/4300587> (accessed 30 January 2018)
Valladares F, Sanchez-Gomez D, Zavala MA (2006) Quantitative estimation of phenotypic plasticity: bridging the gap between the evolutionary concept and its ecological applications. J Ecol 94: 1103-1116
Valladares F, Matesanz S, Guilhaumon F, Araújo MB, Balaguer L, Benito-Garzón M, Cornwell W, Gianoli E, Kleunen M, Naya DE, Nicotra AB, Poorter H, Zavala MA (2014) The effects of phenotypic plasticity and local adaptation on forecasts of species range shifts under climate change. Ecol Lett 17: 1351-1364
Vázquez DP, Gianoli E, Morris WF, Bozinovic F (2017) Ecological and evolutionary impacts of changing climatic variability. Biol Rev 92: 22-42
Walther GR, Post E, Convey P, Menzel A, Parmesan C, Beebee TJC, Fromentin JM, Hoegh-Guldberg O, Bairlein F (2002) Ecological responses to recent climate change. Nature 416: 389-395
Warren RJ, Lake JK (2013) Trait plasticity, not values, best corresponds with woodland plant success in novel and manipulated habitats. J Plant Ecol 6: 201-210
Williams DG, Mack RR, Black RA (1995) Ecophysiology of introduced Pennisetum setaceum on Hawaii: the role of phenotypic plasticity. Ecology 76: 1569-1580
Winter K, Schröppel-Meier G, Caldwell MM (1986) Respiratory CO2 as carbon source for nocturnal acid synthesis at high temperatures in three species exhibiting Crassulacean acid metabolism. Plant Physiol 81: 390-394