Abiotic factors modulate phenotypic plasticity in an apomictic shrub [Miconia albicans (SW.) Triana] along a soil fertility gradient in a Neotropical savanna
Cibele S. Bedetti A B , Débora B. Aguiar A , Maria C. Jannuzzi A , Maria Z. D. Moura A and Fernando A. O. Silveira A B CA Faculdade de Ciências e da Saúde, Centro Universitário UNA, Campus Guajajaras, Belo Horizonte, Minas Gerais, Brazil.
B Departamento de Biologia Vegetal, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Avenida Antônio Carlos 6627, Pampulha, Belo Horizonte, MG 31270-901, Brazil.
C Corresponding author. Email: faosilveira@gmail.com
Australian Journal of Botany 59(3) 274-282 https://doi.org/10.1071/BT10275
Submitted: 15 October 2010 Accepted: 17 March 2011 Published: 9 May 2011
Abstract
Phenotypic plasticity is an important means by which plants cope with environmental heterogeneity; therefore, understanding variation in plant traits in heterogeneous habitats is important to predict responses to changing environments. In this study, we examined the patterns of intraspecific variation in leaf traits of Miconia albicans (Melastomataceae), a widespread, obligatory apomictic shrub, across a soil fertility gradient in the Cerrado (Brazilian savanna). We predicted high plasticity because selection favours high phenotypic plasticity in asexual populations with low genetic variability. Leaves were sampled in campo sujo (grassland), cerrado (savanna) and cerradão (woodland) in south-eastern Brazil during both dry and rainy seasons to calculate leaf area, specific leaf area, leaf tissue thickness, trichome and stomata density. We found significant between-season variation in leaf traits, indicating that the production of season-specific leaves is a strategy to cope with the strong seasonality. Both multivariate analysis and the relative distance plasticity index indicate lower plasticity during the dry season, especially under shade. Our results show that the phenotypic plasticity can be modulated by changes in abiotic factors and the combination of shade and drought can limit the expression of phenotypic plasticity.
References
Bieras AC, Sajo MG (2009) Leaf structure of the cerrado (Brazilian savanna) woody plants. Trees (Berlin) 23, 451–471.| Leaf structure of the cerrado (Brazilian savanna) woody plants.Crossref | GoogleScholarGoogle Scholar |
Boerger MRT, Gluzekar RM, Pil MW, Goldenberg R, Medri M (2008) Leaf morphology variation of Miconia sellowiana (DC.) Naudin (Melastomataceae) in distinct vegetation types at the state of Paraná. Revista Brasileira de Botânica 31, 443–452.
| Leaf morphology variation of Miconia sellowiana (DC.) Naudin (Melastomataceae) in distinct vegetation types at the state of Paraná.Crossref | GoogleScholarGoogle Scholar |
Chen FS, Zeng DH, Fahey TJ, Yao CY, Yu ZY (2010) Response of leaf anatomy of Chenopodium acuminatum to soil resource availability in a semi-arid grassland. Plant Ecology 209, 375–382.
| Response of leaf anatomy of Chenopodium acuminatum to soil resource availability in a semi-arid grassland.Crossref | GoogleScholarGoogle Scholar |
Dickison WC (2000) ‘Integrative plant anatomy.’ (Harcourt Academic Press: San Diego, CA)
Ely F, Torres F, Gaviria J (2005) Relación entre la morfoanatomía foliar de três espécies de Miconia (Melastomataceae) con su hábitat y distribución altitudinal en el parque nacional Sierra Nevada de Mérida, Venezuela. Acta Botanica Venezuelica 28, 275–300.
Feucht W, Schimid PPS, Christ E (1986) Distribution of flavanols in meristematic and mature tissues of Prunus avium shoots. Journal of Plant Physiology 25, 1–8.
Franceschi VR, Nakata PA (2005) Calcium oxalate in plants: formation and function. Annual Review of Plant Biology 56, 41–71.
| Calcium oxalate in plants: formation and function.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXmtVaru74%3D&md5=b4687d747305e095d90302f8eba7dfa9CAS | 15862089PubMed |
Franco AC (2002) Ecophysiology of woody plants. In ‘The Cerrados of Brazil: ecology and natural history of a neotropical savanna’. (Eds PS Oliveira, RJ Marquis) pp. 178–197. (Columbia University Press: New York)
Furley PA (1999) The nature and diversity of neotropical savanna vegetation with particular reference to the Brazilian cerrados. Global Ecology and Biogeography 8, 223–241.
| The nature and diversity of neotropical savanna vegetation with particular reference to the Brazilian cerrados.Crossref | GoogleScholarGoogle Scholar |
Gahan PB (1984) ‘Plant histochemistry and citochemistry: an introduction.’ (Academic Press: London)
Goldenberg R (2004) O gênero Miconia (Melastomataceae) no estado do Paraná. Acta Botanica Brasilica 18, 927–947.
| O gênero Miconia (Melastomataceae) no estado do Paraná.Crossref | GoogleScholarGoogle Scholar |
Goldenberg R, Shepherd GJ (1998) Studies on the reproductive biology of Melastomataceae in cerrado vegetation. Plant Systematics and Evolution 211, 13–29.
| Studies on the reproductive biology of Melastomataceae in cerrado vegetation.Crossref | GoogleScholarGoogle Scholar |
Gonçalves-Alvim SJ, Fernandes GW (2001) Biodiversity of galling insects: historical, community and habitat effects in the Neotropical savanna. Biodiversity and Conservation 10, 79–98.
| Biodiversity of galling insects: historical, community and habitat effects in the Neotropical savanna.Crossref | GoogleScholarGoogle Scholar |
Haridasan M (1988) Performance of Miconia albicans (SW.) Triana, an aluminium accumulating species in acidic and calcareous soils. Communications in Soil Science and Plant Analysis 19, 1091–1103.
| Performance of Miconia albicans (SW.) Triana, an aluminium accumulating species in acidic and calcareous soils.Crossref | GoogleScholarGoogle Scholar |
Howe HF, Westley LC (1990) ‘Ecological relationships of plants and animals.’ (Oxford University Press: New York)
Jensen WA (1962) ‘Botanical histochemistry.’ (Freeman: San Francisco, CA)
Johansen DA (1940) ‘Plant microtechnique.’ (McGraw-Hill Book Co.: New York)
Kraus JE, Arduin M (1997) ‘Manual básico de métodos em Morfologia Vegetal.’ (EDUR: Seropédica)
Lake JA, Quick WP, Beerling DJ, Woodward FI (2001) Signals from mature to new leaves. Nature 411, 154–155.
| Signals from mature to new leaves.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXjslGltLg%3D&md5=b8234737bb5e08c2e86411d59ef65627CAS | 11346781PubMed |
Larcher W (1995) ‘Physiological plant ecology.’ (Springer-Verlag: Berlin)
Lee DW, Oberbauer SF, Johnson P, Khirnapilay B, Mansor M, Mohamad H, Yap SK (2000) Effects of irradiance and spectral quality on leaf structure and function in seedlings of two Southeast Asian Hopea (Dipterocarpaceae) species. American Journal of Botany 87, 447–455.
| Effects of irradiance and spectral quality on leaf structure and function in seedlings of two Southeast Asian Hopea (Dipterocarpaceae) species.Crossref | GoogleScholarGoogle Scholar | 10766716PubMed |
Lemos-Filho JP, Goulart MF, Lovato MB (2008) Populational approach in ecophysiological studies: the case of Plathymenia reticulata, a tree from Cerrado and Atlantic Forest. Brazilian Journal of Plant Physiology 20, 205–216.
| Populational approach in ecophysiological studies: the case of Plathymenia reticulata, a tree from Cerrado and Atlantic Forest.Crossref | GoogleScholarGoogle Scholar |
Marques AR, Garcia QS, Passos Rezende JL, Fernandes GW (2000) Variations of two species of Miconia in the Brazilian cerrado under different light intensities. Tropical Ecology 41, 47–56.
Marquis RJ, Diniz IR, Morais HC (2001) Patterns and correlates of interspecific variation in foliar insect herbivory and pathogen attack in Brazilian Cerrado. Journal of Tropical Ecology 17, 127–148.
| Patterns and correlates of interspecific variation in foliar insect herbivory and pathogen attack in Brazilian Cerrado.Crossref | GoogleScholarGoogle Scholar |
Marquis RJ, Morais HC, Diniz IR (2002) Interactions among cerrado plants and their herbivores: unique or typical? In ‘The Cerrados of Brazil: ecology and natural history of a neotropical savanna’. (Eds PS Oliveira, RJ Marquis) pp. 306–328. (Columbia University Press: New York)
Micro-Optic (2000) ‘Motic Images 2000: version 1.2.’ (CD-ROM) (Micro-optic Industrial Group Corporation: Richmond, Canada)
Nicotra AB, Hermes JP, Jones CS, Schlichting CD (2007) Geographic variation and plasticity to water and nutrients in Pelargonium australe. New Phytologist 176, 136–149.
| Geographic variation and plasticity to water and nutrients in Pelargonium australe.Crossref | GoogleScholarGoogle Scholar | 17803645PubMed |
Oliveira-Filho AT, Ratter JA (2002) Vegetation physiognomies and woody flora of the cerrado biome. In ‘The Cerrados of Brazil: ecology and natural history of a neotropical savanna’. (Eds PS Oliveira, RJ Marquis) pp. 91–120. (Columbia University Press: New York)
Pearce DW, Millard S, Bray DF, Rood SR (2006) Stomatal characteristics of riparian poplar species in a semi-arid environment. Tree Physiology 26, 211–218.
| Stomatal characteristics of riparian poplar species in a semi-arid environment.Crossref | GoogleScholarGoogle Scholar | 16356918PubMed |
Ratter JA, Ribeiro JF, Bridgewater S (1997) The Brazilian cerrado vegetation and threats to its biodiversity. Annals of Botany 80, 223–230.
| The Brazilian cerrado vegetation and threats to its biodiversity.Crossref | GoogleScholarGoogle Scholar |
Reis C, Bieras AC, Sajo MG (2005) Leaf anatomy of Melastomataceae from the cerrado of São Paulo State. Revista Brasileira de Botânica 28, 451–466.
| Leaf anatomy of Melastomataceae from the cerrado of São Paulo State.Crossref | GoogleScholarGoogle Scholar |
Renner SS (1989) A survey of reproductive biology in Neotropical Melastomataceae and Memecylaceae. Annals of the Missouri Botanical Garden 76, 496–518.
| A survey of reproductive biology in Neotropical Melastomataceae and Memecylaceae.Crossref | GoogleScholarGoogle Scholar |
Richards AJ (1997) ‘Plant breeding systems.’ (Chapman & Hall: London)
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. Functional Ecology 20, 207–216.
| Plasticity in leaf traits of 38 tropical tree species in response to light: relationships with light demand and adult stature.Crossref | GoogleScholarGoogle Scholar |
Rossatto DR, Kolb RM (2009) An evergreen neotropical savanna tree (Gochnatia polymorpha, Asteraceae) produces different dry- and wet-season leaf types. Australian Journal of Botany 57, 439–443.
| An evergreen neotropical savanna tree (Gochnatia polymorpha, Asteraceae) produces different dry- and wet-season leaf types.Crossref | GoogleScholarGoogle Scholar |
Rossatto DV, Hoffmann WA, Franco AC (2009) Stomatal traits of cerrado and gallery forest congeneric pairs growing in a transitional region in central Brazil. Acta Botanica Brasilica 23, 499–508.
| Stomatal traits of cerrado and gallery forest congeneric pairs growing in a transitional region in central Brazil.Crossref | GoogleScholarGoogle Scholar |
Sanches MC, Ribeiro SP, Dalvi VC, Barbosa SM, Caldas SH, Lemos-Filho JP (2010) Differential leaf traits of a neotropical tree Cariniana legalis (Mart.) Kuntze (Lecythidaceae): comparing saplings and emergent trees. Trees (Berlin) 24, 79–88.
| Differential leaf traits of a neotropical tree Cariniana legalis (Mart.) Kuntze (Lecythidaceae): comparing saplings and emergent trees.Crossref | GoogleScholarGoogle Scholar |
Sandquist DR, Ehleringer JR (1997) Intraspecific variation of leaf pubescence and drought response in Encelia farinose associated with contrasting desert environments. New Phytologist 135, 635–644.
| Intraspecific variation of leaf pubescence and drought response in Encelia farinose associated with contrasting desert environments.Crossref | GoogleScholarGoogle Scholar |
Scholz FG, Bucci SJ, Goldstein G, Meinzer FC, Franco AC, Salazar A (2008) Plant- and stand-level variation in biophysical and physiological traits along tree density gradients in the Cerrado. Brazilian Journal of Plant Physiology 20, 217–232.
| Plant- and stand-level variation in biophysical and physiological traits along tree density gradients in the Cerrado.Crossref | GoogleScholarGoogle Scholar |
Valladares F, Niinemets Ü (2008) Shade tolerance, a key plant feature of complex nature and consequences. Annual Review of Ecology, Systematics and Evolution 39, 237–257.
| Shade tolerance, a key plant feature of complex nature and consequences.Crossref | GoogleScholarGoogle Scholar |
Valladares F, Gianoli E, Gómez JM (2007) Ecological limits to plant phenotypic plasticity. New Phytologist 176, 749–763.
| Ecological limits to plant phenotypic plasticity.Crossref | GoogleScholarGoogle Scholar | 17997761PubMed |
Valladares F, Sanchez-Gomes D, Zavala MA (2006) Quantitative estimation of phenotypic plasticity. Journal of Ecology 94, 1103–1116.
| Quantitative estimation of phenotypic plasticity.Crossref | GoogleScholarGoogle Scholar |
Vogelman TC, Nishio JN, Smith WK (1996) Leaves and light capture: light propagation and gradients of carbon fixation within leaves. Trends in Plant Science 1, 65–70.
| Leaves and light capture: light propagation and gradients of carbon fixation within leaves.Crossref | GoogleScholarGoogle Scholar |
Zar JH (1996) ‘Biostatistical analysis.’ (Prentice Hall: Upper Saddle River, NJ)